Comparison of pH and counter-ion effect in surfactant-assisted remediation

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初二英语写作风格与文体特色判断练习题40题

初二英语写作风格与文体特色判断练习题40题

初二英语写作风格与文体特色判断练习题40题1.This story is full of vivid descriptions and exciting events. The writing style can be described as________.A.boringB.plainC.livelyD.dull答案:C。

本题考查记叙文写作风格判断。

A 选项boring 意为“无聊的”;B 选项plain 意为“平淡的”;C 选项lively 意为“生动活泼的”;D 选项dull 意为“枯燥的”。

题干中提到故事充满生动的描述和令人兴奋的事件,所以写作风格应是生动活泼的,答案是C。

2.The narrative has a simple plot and straightforward language. The writing style is________.plexB.confusingC.simplisticD.intricate答案:C。

本题考查记叙文写作风格判断。

A 选项complex 意为“复杂的”;B 选项confusing 意为“令人困惑的”;C 选项simplistic 意为“简单的”;D 选项intricate 意为“错综复杂的”。

题干中提到叙事有简单的情节和直白的语言,所以写作风格是简单的,答案是C。

3.The story is told in a slow-paced manner with detailed descriptions.The writing style is________.A.hurriedB.rushedC.leisurelyD.fast-paced答案:C。

本题考查记叙文写作风格判断。

A 选项hurried 意为“匆忙的”;B 选项rushed 意为“急促的”;C 选项leisurely 意为“悠闲的”;D 选项fast-paced 意为“快节奏的”。

药物分析常用英语词汇

药物分析常用英语词汇

药物分析专业英语词汇表Aabsorbance吸收度absorbanceratio吸收度比值absorption吸收absorptioncurve吸收曲线absorptioncoefficient吸收系数accuratevalue准确值Acid—dyecolormcty酸性染料比色法acidimcty酸量法acidity酸度activity活度adjustedretentiontime调整保留时间absorbent吸收剂absorption吸附alkalinity碱度alumina氧化铝,矾土ambienttemperature室温ammoniumthiocyanate硫氰酸铵analyticalqualitycontrol分析质量控制anhydroussubstance 干燥品antioxidant抗氧剂applicationofsample点样areanormalizationmethod面积归一法arsenic砷arsenicsport砷斑assay含量测定assaytolerance含量限度attenuation衰减acidburette酸式滴定管alkaliburette碱式滴定管amortar研钵Bbackextraction反萃取bandabsorption谱带吸收batch批batchnumber批号Benttendorlfmethod白田道夫法betweendayprecision日间密度精biotransformation生物转化blanktest空白试验boilingrange沸程BritishPharmacopeia英国药典bromatetitration溴酸盐滴定法brominemethod溴量法bromothymolblue溴麝香酚蓝bulkdrug原料药by—product副产物breaker烧杯buretteglassbeadnozzle滴定管brownacidburette棕色酸式滴定管Ccalibrationcurve校正曲线calomelelectrode甘汞电极calorimetry量热分析capacityfactor容量因子capillarygaschromatography毛细管气相色谱法carriergas载气characteristicsdescription性状chelatecompound螯合物chemicalequivalent化学当量Chinesepharmacopeia中国药典Chinesematerialmedicine中成药Chinesematerialmidicalpreparation中药制剂chiral手性的chiralcarbonatom手性碳原子chromatogram色谱图chromatography色谱法chromatographiccolumn色谱柱chromatographiccondition色谱条件clarity澄清度coefficientofdistribution分配系数coefficientofvariation变异系数colorchangeinterval变色范围colorreaction显色反应colormetry比色法columnefficiency柱效columntemperature柱温comparativetest比较试验completenessofsolution溶液的澄清度conjugate缀合物concentration—timecurve浓度时间曲线confidenceinterval置信区间confidencelevel置信水平controlledtrial对照试验correlationcoefficient相关系数contrasttest对照试验congealingpoint凝点contentunifarmity装量差异controlledtrial对照试验correlationcoefficient相关系数contrasttest对照试验counterion反离子cresalred甲酚红cuvettecell比色池cyanide氰化物casserolesmall勺皿Ddead—stoptitration永定滴定法deadtime死时间deflection偏差deflectionpoint拐点degassing脱气deionizedwater去离子水deliquescence潮解depressorsubstancestest降压物质检查法desiccant干燥剂detection检查developingreagent展开剂developingchamber展开室deviation偏差dextrose右旋糖diastereoisomer非对映异构体diazotization重氮化differentialthermalanalysis差示热分析法differentialscanningcalorimetry差示扫描热法Gutzeit古蔡daytodayprecision日间精密度dissolution溶出度directinjection直接进样2,6-dichlorindophenoltitration2,6-二氯靛酚滴定法digestion消化diphastictitration双向滴定disintegrationtest崩解试验dispersion分散度dissolubility溶解度dissolutiontest溶解度检查distillingrange滴程distributionchromatography分配色谱dose剂量drugqualitycontrol药品质量控制dryingtoconstantweight干燥至恒重duplicatetest重复试验diskmethodwatermethod压片法Eeffectiveconstituent有效成分effectiveplatenumber有效板数effectiveofcolumn柱效electrophoresis电泳elimination消除eluate洗脱液elution洗脱enamtiomer对映体endabsorption末端吸收endogenoussubstances内源性物质enzymedrug酶类药物enzymeinduction酶诱导enzymeinhibition酶抑制epimer差向异构体equilibriumconstant平衡常数errorinvolumetricanalysis容量分析误差exclusionchromatography排阻色谱法expirationdate失效期externalstandardmethod外标法extract提取物extrationgravimetry提取重量法extractiontitration提取容量法extrapolatedmethod外插法Erlenmeyerflask锥形瓶evaporatingdishsmall蒸发皿elongatedbulb胖肚electronicbalanceMettlerAL204MettlerAL204电子天平Ffactor系数fehling’sreaction斐林实验filter过滤finenessoftheparticles颗粒细度flowrate流速fluorescentagent荧光剂fluorescencespectrophotometry荧光分光光度法fluorescencedetection荧光检测器fluorescenceanalysis荧光分析法foreignpigment有色杂质formulary处方集free游离freezingtest冻结试验fusedsilica熔融石英filterpaper滤纸Ggaschromatography气相色谱法gas-liquidchromatography气液色谱法gaspurifier气体净化器Generalidentificationtest一般鉴别试验generalnotices凡例Generalrequirements(药典)通则goodclinicalpractices药品临床管理规范goodlaboratorypractices药品实验室管理规范goodmanufacturingpractices(GMP)药品生产质量管理规范goodsupplypractices(GSP)药品供应管理规范gradientelution梯度洗脱grating光栅gravimetricmethod重量法Gutzeittest古蔡(检砷)法glassfunnellongstem玻璃漏斗gradcylinder量筒glassrod玻棒graduatedpipettes刻度吸管GC气相色谱Hheavymetal重金属halfpeakwidth平峰宽heatconductivity热导率heightequivalenttoatheoreticalplate理论塔板高度heightofaneffectiveplate有效塔板高度high-performanceliquidchromatography(HPLC)高效液相色谱法high-performancethin-layerchromatography(HPTLC)高效薄层色谱法hydrate水合物hydrolysis水解hydrophilicity亲水性hydrophobicity疏水性hydroxylvalue羟值hyperchromiceffect浓色效应hypochromiceffect淡色效应HHS-typeconstanttemperaturewaterbathHHS型恒温水锅HPLC高效液相色谱法Iidentification鉴别ignitiontoconstantweight灼烧至恒重immobilephase固定相immunoassay免疫测定impurity杂质inactivation失活index索引indicatorelectrode指示电极indicator指示剂inhibitor抑制剂injectingseptum进样隔膜胶垫instrumentalanalysis仪器分析injectionvalue进样阀insulinassay胰岛素生物检测法integrator积分仪intercept截距interface接口internalstandardsubstance内标物质Internationalunit国际单位invitro体外invivo体内iodide碘化物iodoformreation碘仿反应iodometry碘量法ionpairchromatography离子对色谱ionsuppression离子抑制ionsuppression离子抑制ionicstrength离子强度ion-pairingagent离子对试剂ionization电离isoabsorptivepoint等吸收点isocraticelution等溶剂组成洗脱isoelectricpoint等电点isoosmoticsolution等渗溶液irreversibleindicator不可逆指示剂irreversiblepotential不可逆电位KKarlFischertitration卡尔-费舍尔滴定Kjeldahlmethodfornitrogen凯氏定氮法Koberreagent 科伯试剂Kovatsretentionindex科瓦茨保留指数Llabelledamount标示量leadingpeak前延峰levelingeffect均化效应licensedpharmacist执业药师limitcontrol限量控制limitofdetection检测限limitofquantitation定量限limittest杂质限度试验lossondrying干燥失重lowpressuregradientpump氧压梯度泵linearityandrange线性及范围linearityscanning线性扫描luminescence发光litmuspaper石蕊试纸lyophilization冷冻干燥Mmainconstituent主成分make-upgas尾吹气maltolreaction麦芽酚试验Marquistest马奎斯试验massanalyzerdetector质量分析检测器massspectrometricanalysis质谱分析massspectrum质谱图meandeviation平均偏差meltingpoint熔点meltingrange熔距metabolite代谢物metastableion亚稳离子micellarchromatography胶束色谱法microanalysis微量分析microcrystal微晶microdialysis微透析migrationtime迁移时间Milliporefiltration微孔过滤mobilephase流动相molecularformula分子式monitor检测monochromator单色器monographs正文Nnaturalproduct天然产物Nessler’sreagent碱性碘化汞试液neutralization中和nitrogencontent总氮量nonaqueousacid-basetitration非水酸碱滴定nonprescriptiondrug,overthecounterdrugs非处方药nonspecificimpurity一般杂质non-volatilematter不挥发物normalphase正相normalization归一化法Nesslercolorcomparisontube纳氏比色管Onotice凡例octadecylsilanebondedsilicagel十八烷基硅烷键合硅胶odorless辛基硅烷odorless无臭officialname法定名officialtest法定试验on-columndetector柱上检测器on-columninjection柱头进样onthedriedbasis按干燥品计opalescence乳浊opticalactivity光学活性opticalisomerism旋光异构opticalpurity光学纯度organicvolatileimpurities有机挥发性杂质orthogonaltest正交试验orthophenanthroline邻二氮菲outlier可疑数据overtones倍频封oxidation-reductiontitration氧化还原滴定oxygenflaskcombustion氧瓶燃烧Ppackedcolumn填充柱packingmaterial色谱柱填料palladiumioncolorimetry钯离子比色法parention母离子particulatematter不溶性微粒partitioncoefficient分配系数patternrecognition(ppm)百万分之几peaksymmetry峰不对称性peakvalley峰谷peakwidthathalfheight半峰宽percenttransmittance透光百分率pHindicatorabsorbanceratiomethodpH指示剂吸光度比值法pharmaceuticalanalysis药物分析pharmacopeia药典pharmacy药学photometer光度计polarimetry旋光测定法polarity极性polydextrangel葡聚糖凝胶potentiometer电位计potentiometrictitration电位滴定法precipitationform沉淀形式precision精密度preparation制剂prescriptiondrug处方药pretreatment预处理primarystandard基准物质principalcomponentanalysis主成分分析prototypedrug原型药物purification纯化purity纯度pyrogen热原pycnometermethod比重瓶法plasticwashbottle洗瓶platformbalance天平pipette移液管pyknowmeterflasks容量瓶Qqualitycontrol质量控制qualityevaluation质量评价qualitystandard质量标准quantitativedetermination定量测定quantitativeanalysis定量分析quasi-molecularion准分子离子Rracemization消旋化randomsampling随机抽样rationaluseofdrug合理用药readilycarbonizablesubstance易炭化物质reagentsprayer试剂喷雾剂recovery回收率referenceelectrode参比电极relatedsubstance相关物质relativedensity相对密度relativeintensity相对强度repeatability重复性replicatedetermination平行测定reproducibility重现性residualbasichydrolysismethod剩余碱水解法residualliquidjunctionpotential残余液接电位residualtitration剩余滴定residuceonignition炽灼残渣resolution分辨率responsetime响应时间retention保留reversedphasechromatography反相色谱法reverseosmosis反渗透rinse淋洗robustness可靠性round修约reagentbottles试剂瓶roundbottomflask圆底烧瓶rubbersuctionbulb洗耳球Ssafety安全性Sakaguchitest坂口试验saltbridge盐桥saltingout盐析sampleapplicator点样器sampleapplication点样sampling取样saponificationvalue皂化值saturatedcalomelelectrode饱和甘汞电极selectivity选择性significantdifference显着性水平significanttesting显着性检验silicaget硅胶silverchlorideelectrode氯化银电极similarity相似性sodiumdodecylsulfate十二基酸钠solid-phaseextraction固相萃取solubility溶解度specificabsorbance吸收系数specification规格specificity专属性specificrotation比旋度specificweight比重spiked加入标准的splitinjection分流进样sprayreagent显色剂stability稳定性standardcolorsolution标准比色液standarddeviation标准差standardization标定standardsubstance标准品statisticalerror统计误差sterilitytest无菌试验stocksolution储备液stoichiometricpoint化学计量点storage贮藏straylight杂散光substrate底物substituent取代基sulfate硫酸盐sulphatedash硫酸盐灰分support载体suspension旋浊度swellingdegree膨胀度symmetryfactor对称因子systematicerror系统误差separatingfunnel分液漏斗stopcock玻璃活塞scissors剪刀spiritlamp酒精灯silicagelGthinlayer硅胶G薄层板Ttable片剂tailingfactor拖尾因子tailingpeak拖尾峰testsolution试液thermalanalysis热分析法thermalconductivitydetector热导检测器thermogravimetricanalysis热重分析法TheUnitedStatesPharmacopoeia美国药典ThePharmacopoeiaofJapan日本药局方thinlayerchromatography薄层色谱thiochromereaction硫色素反应thymol百里酚thymolphthalein百里酚酞titer滴定度three-dimensionalchromatogram三维色谱图titrant滴定剂titrationerror滴定误差titrimetricanalysis滴定分析法tolerance容许限totalash总灰分totalqualitycontrol全面质量控制traditionaldrugs传统药traditionalChinesemedicine中药turbidance浑浊turbidimetricassay浊度测定法turbidimetry比浊度turbidity浊度Uultracentrifugation超速离心ultravioletirradiation紫外线照射unduetoxicity异常毒性uniformdesign均匀设计uniformityofdosageunits含量均匀度uniformityofvolume装量均匀性uniformityofweight重量均匀性Vvalidity可靠性variance方差viscosity粘度volatileoildeterminationapparatus挥发油测定器volatilization挥发性volumetricanalysis容量分析volumetricsolution滴定液volumetricflasks比重瓶Wwavelength波长wavenumber波数weighingbottle称量瓶weighingform称量形式well-closedcontainer密闭容器whiteboard白瓷板XxylenecyanolblueFF二甲苯蓝FFxylenolorange二甲酚橙ZZigzagscanning锯齿扫描zwitterions两性离子Zymolysis酶解作用zoneelectrophoresis区带电泳。

药物分析报告常用英语词汇

药物分析报告常用英语词汇

药物分析专业英语词汇表Aabsorbance 吸收度absorbance ratio 吸收度比值absorption 吸收absorption curve 吸收曲线absorption coefficient 吸收系数accurate value 准确值Acid—dye colormcty 酸性染料比色法acidimcty 酸量法acidity 酸度activity 活度adjusted retention time 调整保留时间absorbent 吸收剂absorption吸附alkalinity 碱度alumina 氧化铝,矾土ambient temperature 室温ammonium thiocyanate 硫氰酸铵analytical quality control 分析质量控制anhydrous substance 干燥品antioxidant 抗氧剂application of sample 点样area normalization method 面积归一法arsenic砷arsenic sport 砷斑assay 含量测定assay tolerance 含量限度attenuation 衰减acid burette 酸式滴定管alkali burette 碱式滴定管a mortar 研钵Bback extraction 反萃取band absorption 谱带吸收batch 批batch number 批号Benttendorlf method 白田道夫法between day precision 日间密度精biotransformation 生物转化blank test 空白试验boiling range 沸程British Pharmacopeia 英国药典bromate titration 溴酸盐滴定法bromine method 溴量法bromothymol blue 溴麝香酚蓝bulk drug 原料药by—product 副产物breaker 烧杯burette glass bead nozzle 滴定管brown acid burette 棕色酸式滴定管Ccalibration curve 校正曲线calomel electrode 甘汞电极calorimetry 量热分析capacity factor 容量因子capillary gas chromatography 毛细管气相色谱法carrier gas 载气characteristics description 性状chelate compound 螯合物chemical equivalent 化学当量Chinese pharmacopeia 中国药典Chinese material medicine 中成药Chinese material midical preparation 中药制剂chiral 手性的chiral carbon atom 手性碳原子chromatogram 色谱图chromatography 色谱法chromatographic column 色谱柱chromatographic condition 色谱条件clarity 澄清度coefficient of distribution 分配系数coefficient of variation 变异系数color change interval 变色范围color reaction 显色反应colormetry 比色法column efficiency 柱效column temperature 柱温comparative test 比较试验completeness of solution 溶液的澄清度conjugate 缀合物concentration—time curve 浓度时间曲线confidence interval 置信区间confidence level 置信水平controlled trial 对照试验correlation coefficient 相关系数contrast test 对照试验congealing point 凝点content unifarmity装量差异controlled trial 对照试验correlation coefficient 相关系数contrast test 对照试验counter ion 反离子cresal red 甲酚红cuvette cell 比色池cyanide氰化物casserole small 勺皿Ddead—stop titration 永定滴定法dead time 死时间deflection 偏差deflection point 拐点degassing 脱气deionized water 去离子水deliquescence 潮解depressor substances test 降压物质检查法desiccant 干燥剂detection 检查developing reagent 展开剂developing chamber 展开室deviation 偏差dextrose 右旋糖diastereoisomer 非对映异构体diazotization 重氮化differential thermal analysis 差示热分析法differential scanning calorimetry 差示扫描热法Gutzeit 古蔡day to day precision 日间精密度dissolution 溶出度direct injection 直接进样2,6-dichlorindophenol titration 2,6-二氯靛酚滴定法digestion 消化diphastic titration 双向滴定disintegration test 崩解试验dispersion 分散度dissolubility 溶解度dissolution test 溶解度检查distilling range 滴程distribution chromatography 分配色谱dose 剂量drug quality control 药品质量控制drying to constant weight 干燥至恒重duplicate test 重复试验disk method water method 压片法Eeffective constituent 有效成分effective plate number 有效板数effective of column 柱效electrophoresis 电泳elimination 消除eluate 洗脱液elution 洗脱enamtiomer 对映体end absorption 末端吸收endogenous substances 内源性物质enzyme drug 酶类药物enzyme induction 酶诱导enzyme inhibition 酶抑制epimer 差向异构体equilibrium constant 平衡常数error in volumetric analysis 容量分析误差exclusion chromatography 排阻色谱法expiration date 失效期external standard method 外标法extract 提取物extration gravimetry 提取重量法extraction titration 提取容量法extrapolated method外插法Erlenmeyer flask 锥形瓶evaporating dish small 蒸发皿elongated bulb 胖肚electronic balance MettlerAL204 MettlerAL204电子天平Ffactor 系数fehling’s reaction 斐林实验filter 过滤fineness of the particles 颗粒细度flow rate 流速fluorescent agent 荧光剂fluorescence spectrophotometry 荧光分光光度法fluorescence detection 荧光检测器fluorescence analysis 荧光分析法foreign pigment 有色杂质formulary 处方集free 游离freezing test 冻结试验fused silica 熔融石英filter paper 滤纸Ggas chromatography 气相色谱法gas-liquid chromatography 气液色谱法gas purifier 气体净化器General identification test 一般鉴别试验general notices 凡例General requirements (药典) 通则good clinical practices 药品临床管理规范good laboratory practices 药品实验室管理规范good manufacturing practices(GMP) 药品生产质量管理规范good supply practices(GSP) 药品供应管理规范gradient elution 梯度洗脱grating 光栅gravimetric method 重量法Gutzeit test 古蔡(检砷)法glass funnel long stem 玻璃漏斗grad cylinder 量筒glass rod 玻棒graduated pipettes 刻度吸管GC 气相色谱Hheavy metal 重金属half peak width 平峰宽heat conductivity 热导率height equivalent to a theoretical plate 理论塔板高度height of an effective plate 有效塔板高度high-performance liquid chromatography (HPLC)高效液相色谱法high-performance thin-layer chromatography (HPTLC)高效薄层色谱法hydrate 水合物hydrolysis 水解hydrophilicity 亲水性hydrophobicity 疏水性hydroxyl value 羟值hyperchromic effect 浓色效应hypochromic effect 淡色效应HHS-type constant temperature water bath HHS型恒温水锅HPLC 高效液相色谱法Iidentification 鉴别ignition to constant weight 灼烧至恒重immobile phase 固定相immunoassay 免疫测定impurity 杂质inactivation 失活index 索引indicator electrode 指示电极indicator 指示剂inhibitor 抑制剂injecting septum 进样隔膜胶垫instrumental analysis 仪器分析injection value 进样阀insulin assay 胰岛素生物检测法integrator 积分仪intercept 截距interface 接口internal standard substance 内标物质International unit 国际单位in vitro 体外in vivo 体内iodide 碘化物iodoform reation 碘仿反应iodometry 碘量法ion pair chromatography 离子对色谱ion suppression 离子抑制ion suppression 离子抑制ionic strength 离子强度ion-pairing agent 离子对试剂ionization 电离isoabsorptive point 等吸收点isocratic elution 等溶剂组成洗脱isoelectric point 等电点isoosmotic solution 等渗溶液irreversible indicator 不可逆指示剂irreversible potential 不可逆电位KKarl Fischer titration 卡尔-费舍尔滴定Kjeldahl method for nitrogen 凯氏定氮法Kober reagent 科伯试剂Kovats retention index 科瓦茨保留指数Llabelled amount 标示量leading peak 前延峰leveling effect 均化效应licensed pharmacist 执业药师limit control 限量控制limit of detection 检测限limit of quantitation 定量限limit test 杂质限度试验loss on drying 干燥失重low pressure gradient pump 氧压梯度泵linearity and range 线性及范围linearity scanning 线性扫描luminescence 发光litmus paper 石蕊试纸lyophilization 冷冻干燥Mmain constituent 主成分make-up gas 尾吹气maltol reaction 麦芽酚试验Marquis test 马奎斯试验mass analyzer detector 质量分析检测器mass spectrometric analysis 质谱分析mass spectrum 质谱图mean deviation 平均偏差melting point 熔点melting range 熔距metabolite 代谢物metastable ion 亚稳离子micellar chromatography 胶束色谱法microanalysis 微量分析microcrystal 微晶microdialysis 微透析migration time 迁移时间Millipore filtration 微孔过滤mobile phase 流动相molecular formula 分子式monitor 检测monochromator 单色器monographs 正文Nnatural product 天然产物Nessler’s reagent 碱性碘化汞试液neutralization 中和nitrogen content 总氮量nonaqueous acid-base titration 非水酸碱滴定nonprescription drug ,over the counter drugs 非处方药nonspecific impurity 一般杂质non-volatile matter 不挥发物normal phase 正相normalization 归一化法Nessler color comparison tube 纳氏比色管Onotice 凡例octadecyl silane bonded silicagel 十八烷基硅烷键合硅胶odorless 辛基硅烷odorless 无臭official name 法定名official test 法定试验on-column detector 柱上检测器on-column injection 柱头进样on the dried basis 按干燥品计opalescence 乳浊optical activity 光学活性optical isomerism 旋光异构optical purity 光学纯度organic volatile impurities 有机挥发性杂质orthogonal test 正交试验orthophenanthroline 邻二氮菲outlier 可疑数据overtones 倍频封oxidation-reduction titration 氧化还原滴定oxygen flask combustion 氧瓶燃烧Ppacked column 填充柱packing material 色谱柱填料palladium ion colorimetry 钯离子比色法parent ion 母离子particulate matter 不溶性微粒partition coefficient 分配系数pattern recognition(ppm)百万分之几peak symmetry 峰不对称性peak valley 峰谷peak width at half height 半峰宽percent transmittance 透光百分率pH indicator absorbance ratio method pH指示剂吸光度比值法pharmaceutical analysis 药物分析pharmacopeia 药典pharmacy 药学photometer 光度计polarimetry 旋光测定法polarity 极性polydextran gel 葡聚糖凝胶potentiometer 电位计potentiometric titration 电位滴定法precipitation form 沉淀形式precision 精密度preparation 制剂prescription drug 处方药pretreatment 预处理primary standard 基准物质principal component analysis 主成分分析prototype drug 原型药物purification 纯化purity 纯度pyrogen 热原pycnometer method 比重瓶法plastic wash bottle 洗瓶platform balance 天平pipette 移液管pyknowmeter flasks 容量瓶Qquality control 质量控制quality evaluation 质量评价quality standard 质量标准quantitative determination 定量测定quantitative analysis 定量分析quasi-molecular ion 准分子离子Rracemization 消旋化random sampling 随机抽样rational use of drug 合理用药readily carbonizable substance 易炭化物质reagent sprayer 试剂喷雾剂recovery 回收率reference electrode 参比电极related substance 相关物质relative density 相对密度relative intensity 相对强度repeatability 重复性replicate determination 平行测定reproducibility 重现性residual basic hydrolysis method 剩余碱水解法residual liquid junction potential 残余液接电位residual titration 剩余滴定residuce on ignition 炽灼残渣resolution 分辨率response time 响应时间retention 保留reversed phase chromatography 反相色谱法reverse osmosis 反渗透rinse 淋洗robustness 可靠性round 修约reagent bottles 试剂瓶round bottom flask 圆底烧瓶rubber suction bulb 洗耳球Ssafety 安全性Sakaguchi test 坂口试验salt bridge 盐桥salting out 盐析sample applicator 点样器sample application 点样sampling 取样saponification value 皂化值saturated calomel electrode 饱和甘汞电极selectivity 选择性significant difference 显著性水平significant testing 显著性检验silica get 硅胶silver chloride electrode 氯化银电极similarity 相似性sodium dodecylsulfate 十二基酸钠solid-phase extraction 固相萃取solubility 溶解度specific absorbance 吸收系数specification 规格specificity 专属性specific rotation 比旋度specific weight 比重spiked 加入标准的split injection 分流进样spray reagent 显色剂stability 稳定性standard color solution 标准比色液standard deviation 标准差standardization 标定standard substance 标准品statistical error 统计误差sterility test 无菌试验stock solution 储备液stoichiometric point 化学计量点storage 贮藏stray light 杂散光substrate 底物substituent 取代基sulfate 硫酸盐sulphated ash 硫酸盐灰分support 载体suspension 旋浊度swelling degree 膨胀度symmetry factor 对称因子systematic error 系统误差separating funnel 分液漏斗stopcock 玻璃活塞scissors 剪刀spirit lamp 酒精灯silica gel G thin layer 硅胶G薄层板Ttable 片剂tailing factor 拖尾因子tailing peak 拖尾峰test solution 试液thermal analysis 热分析法thermal conductivity detector 热导检测器thermogravimetric analysis 热重分析法The United States Pharmacopoeia 美国药典The Pharmacopoeia of Japan 日本药局方thin layer chromatography 薄层色谱thiochrome reaction 硫色素反应thymol 百里酚thymolphthalein 百里酚酞titer 滴定度three-dimensional chromatogram 三维色谱图titrant 滴定剂titration error 滴定误差titrimetric analysis 滴定分析法tolerance 容许限total ash 总灰分total quality control 全面质量控制traditional drugs 传统药traditional Chinese medicine 中药turbidance 浑浊turbidimetric assay 浊度测定法turbidimetry 比浊度turbidity 浊度Uultracentrifugation 超速离心ultraviolet irradiation 紫外线照射undue toxicity 异常毒性uniform design 均匀设计uniformity of dosage units 含量均匀度uniformity of volume 装量均匀性uniformity of weight 重量均匀性Vvalidity 可靠性variance 方差viscosity 粘度volatile oil determination apparatus 挥发油测定器volatilization 挥发性volumetric analysis 容量分析volumetric solution 滴定液volumetric flasks 比重瓶Wwave length 波长wave number 波数weighing bottle 称量瓶weighing form 称量形式well-closed container 密闭容器white board 白瓷板Xxylene cyanol blue FF 二甲苯蓝FF xylenol orange 二甲酚橙ZZigzag scanning 锯齿扫描zwitterions 两性离子Zymolysis 酶解作用zone electrophoresis 区带电泳。

CFA名词字典

CFA名词字典

公开市场委员会 公开市场操作 公开喊价 开放式基金 未平仓合约数 开放型投资公司 开口抵押 开盘价格 营运资产 营业预算 流动资本 营运现金流量 抽样特性曲线 营业成本 营业周期 营运效率比率 营业费用 经营暴露 营业收益 经营性租赁 经营杠杆 营业损失 经营管理 经营合并 营业利润率 营运利润比率 公积金 损益表 营业收益 机会成本 股本资本的机会成本 生产的机会成本 机会集合 最佳资本结构 最优股利政策 最优资产组合
应付账款周转率 回收时间 回收期法 收款人 支付型互换期权 支付固定方 债券 后续支付期权 支付日 付款净值结算 实物支付 损益 支付矩阵/矩阵 股利发放率 工资支付计划 波峰 同行比较法 盯住 钉住汇率 盯住汇率制 固定价格 定价 养老基金 养老金计划 养老金 条形图 应收帐款百分比法 完成百分比法 百分数 完全共线性 完全避险 完美市场 奖励费 履约保证 业绩评估 绩效费用
最优化 最佳产量 期权 期权买方 期权合约 期权成本 期货合约期权 期货期权 实物期权 期权单 期权费 期权定价模型 期权卖方 期权系列 期权卖方 期权调整价差 无期权债券 期权清算公司 期权市场 指令簿处理人员 指令驱动系统 序列测定 序列测定 普通年金 普通业务 最小二乘法 最初发行的折扣债券 原始押金 序数效用 其他支票存款 其他综合损益 其他退休福利 其他收入 其他因素不变 其他情况不变 差错交易
Optimizer Optimum capacity Option Option buyer Option contract Option cost Option on a futures contact Option on futures Option on the physical Option orders Option premium (or option price or premium) Option Pricing Model (OPM) Option seller Option series Option writer Option-adjusted spread (OAS) Option-free bond Options Clearing Corporation (OCC) Options market Order book official Order-driven system Ordinal level data Ordinal scale Ordinary annuity Ordinary business Ordinary least squares (OLS) Original issue discount bond Original margin Orinal utility Other Checkable Depoists ( OCD ) Other comprehensive income Other postretirement benefits Other revenues Other things constant Other things equal Out trade

常用分析化学专业英语词汇

常用分析化学专业英语词汇

常用分析化学专业英语词汇absorbance 吸光度absorbent 吸附剂absorption curve 吸收曲线absorption peak 吸收峰absorptivity 吸收系数accident error 偶然误差accuracy 准确度acid-base titration 酸碱滴定acidic effective coefficient 酸效应系数acidic effective curve 酸效应曲线acidity constant 酸度常数activity 活度activity coefficient 活度系数adsorption 吸附adsorption indicator 吸附指示剂affinity 亲和力aging 陈化amorphous precipitate 无定形沉淀amphiprotic solvent 两性溶剂amphoteric substance 两性物质amplification reaction 放大反应analytical balance 分析天平analytical chemistry 分析化学analytical concentration 分析浓度analytical reagent (AR) 分析试剂apparent formation constant 表观形成常数aqueous phase 水相argentimetry 银量法ashing 灰化atomic spectrum 原子光谱autoprotolysis constant 质子自递常数auxochrome group 助色团back extraction 反萃取band spectrum 带状光谱bandwidth 带宽bathochromic shift 红移blank 空白blocking of indicator 指示剂的封闭bromometry 溴量法buffer capacity 缓冲容量buffer solution 缓冲溶液burette 滴定管calconcarboxylic acid 钙指示剂calibrated curve 校准曲线calibration 校准catalyzed reaction 催化反应cerimetry 铈量法charge balance 电荷平衡chelate 螯合物chelate extraction 螯合物萃取chemical analysis 化学分析chemical factor 化学因素chemically pure 化学纯chromatography 色谱法chromophoric group 发色团coefficient of variation 变异系数color reagent 显色剂color transition point 颜色转变点colorimeter 比色计colorimetry 比色法column chromatography 柱色谱complementary color 互补色complex 络合物complexation 络合反应complexometry complexometric titration 络合滴定法complexone 氨羧络合剂concentration constant 浓度常数conditional extraction constant 条件萃取常数conditional formation coefficient 条件形成常数conditional potential 条件电位conditional solubility product 条件溶度积confidence interval 置信区间confidence level 置信水平conjugate acid-base pair 共轭酸碱对constant weight 恒量contamination 沾污continuous extraction 连续萃取continuous spectrum 连续光谱coprecipitation 共沉淀correction 校正correlation coefficient 相关系数crucible 坩埚crystalline precipitate 晶形沉淀cumulative constant 累积常数curdy precipitate 凝乳状沉淀degree of freedom 自由度demasking 解蔽derivative spectrum 导数光谱desiccant; drying agent 干燥剂desiccator 保干器determinate error 可测误差deuterium lamp 氘灯deviation 偏差deviation average 平均偏差dibasic acid 二元酸dichloro fluorescein 二氯荧光黄dichromate titration 重铬酸钾法dielectric constant 介电常数differential spectrophotometry 示差光度法differentiating effect 区分效应dispersion 色散dissociation constant 离解常数distillation 蒸馏distribution coefficient 分配系数distribution diagram 分布图distribution ratio 分配比double beam spectrophotometer 双光束分光光度计dual-pan balance 双盘天平dual-wavelength spectrophotometry 双波长分光光度法electronic balance 电子天平electrophoresis 电泳eluent 淋洗剂end point 终点end point error 终点误差enrichment 富集eosin 曙红equilibrium concentration 平衡浓度equimolar series method 等摩尔系列法Erelenmeyer flask 锥形瓶eriochrome black T (EBT) 铬黑T error 误差ethylenediamine tetraacetic acid (EDTA) 乙二胺四乙酸evaporation dish 蒸发皿exchange capacity 交换容量extent of crosslinking 交联度extraction constant 萃取常数extraction rate 萃取率extraction spectrphotometric method 萃取光度法Fajans method 法杨斯法ferroin 邻二氮菲亚铁离子filter 漏斗filter 滤光片filter paper 滤纸filtration 过滤fluex 溶剂fluorescein 荧光黄flusion 熔融formation constant 形成常数frequency 频率frequency density 频率密度frequency distribution 频率分布gas chromatography (GC) 气相色谱grating 光栅gravimetric factor 重量因素gravimetry 重量分析guarantee reagent (GR) 保证试剂high performance liquid chromatography (HPLC) 高效液相色谱histogram 直方图homogeneous precipitation 均相沉淀hydrogen lamp 氢灯hypochromic shift 紫移ignition 灼烧indicator 指示剂induced reaction 诱导反应inert solvent 惰性溶剂instability constant 不稳定常数instrumental analysis 仪器分析intrinsic acidity 固有酸度intrinsic basicity 固有碱度intrinsic solubility 固有溶解度iodimetry 碘滴定法iodine-tungsten lamp 碘钨灯iodometry 滴定碘法ion association extraction 离子缔合物萃取ion chromatography (IC) 离子色谱ion exchange 离子交换ion exchange resin 离子交换树脂ionic strength 离子强度isoabsorptive point 等吸收点Karl Fisher titration 卡尔•费歇尔法Kjeldahl determination 凯氏定氮法Lambert-Beer law 朗泊-比尔定律leveling effect 拉平效应ligand 配位体light source 光源line spectrum 线状光谱linear regression 线性回归liquid chromatography (LC) 液相色谱macro analysis 常量分析masking 掩蔽masking index 掩蔽指数mass balance 物料平衡matallochromic indicator 金属指示剂maximum absorption 最大吸收mean, average 平均值measured value 测量值measuring cylinder 量筒measuring pipette 吸量管median 中位数mercurimetry 汞量法mercury lamp 汞灯mesh [筛]目methyl orange (MO) 甲基橙methyl red (MR) 甲基红micro analysis 微量分析mixed constant 混合常数mixed crystal 混晶mixed indicator 混合指示剂mobile phase 流动相Mohr method 莫尔法molar absorptivity 摩尔吸收系数mole ratio method 摩尔比法molecular spectrum 分子光谱monoacid 一元酸monochromatic color 单色光monochromator 单色器neutral solvent 中性溶剂neutralization 中和non-aqueous titration 非水滴定normal distribution 正态分布occlusion 包藏organic phase 有机相ossification of indicator 指示剂的僵化outlier 离群值oven 烘箱paper chromatography(PC) 纸色谱parallel determination 平行测定path lenth 光程permanganate titration 高锰酸钾法phase ratio 相比phenolphthalein (PP) 酚酞photocell 光电池photoelectric colorimeter 光电比色计photometric titration 光度滴定法photomultiplier 光电倍增管phototube 光电管pipette 移液管polar solvent 极性溶剂polyprotic acid 多元酸population 总体postprecipitation 后沉淀precipitant 沉淀剂precipitation form 沉淀形precipitation titration 沉淀滴定法precision 精密度preconcentration 预富集predominance-area diagram 优势区域图primary standard 基准物质prism 棱镜probability 概率proton 质子proton condition 质子条件protonation 质子化protonation constant 质子化常数purity 纯度qualitative analysis 定性分析quantitative analysis 定量分析quartering 四分法random error 随机误差range 全距(极差)reagent blank 试剂空白Reagent bottle 试剂瓶recording spectrophotometer 自动记录式分光光度计recovery 回收率redox indicator 氧化还原指示剂redox titration 氧化还原滴定referee analysis 仲裁分析reference level 参考水平reference material (RM) 标准物质reference solution 参比溶液relative error 相对误差resolution 分辨力rider 游码routine analysis 常规分析sample 样本,样品sampling 取样self indicator 自身指示剂semimicro analysis 半微量分析separation 分离separation factor 分离因数side reaction coefficient 副反应系数significance test 显著性检验significant figure 有效数字simultaneous determination of multiponents 多组分同时测定single beam spectrophotometer 单光束分光光度计single-pan balance 单盘天平slit 狭缝sodium diphenylamine sulfonate 二苯胺磺酸钠solubility product 溶度积solvent extraction 溶剂萃取species 型体(物种)specific extinction coefficient 比消光系数spectral analysis 光谱分析spectrophotometer 分光光度计spectrophotometry 分光光度法stability constant 稳定常数standard curve 标准曲线standard deviation 标准偏差standard potential 标准电位standard series method 标准系列法standard solution 标准溶液standardization 标定starch 淀粉stationary phase 固定相steam bath 蒸气浴stepwise stability constant 逐级稳定常数stoichiometric point 化学计量点structure analysis 结构分析supersaturation 过饱和systematic error 系统误差test solution 试液thermodynamic constant 热力学常数thin layer chromatography (TLC) 薄层色谱titrand 被滴物titrant 滴定剂titration 滴定titration constant 滴定常数titration curve 滴定曲线titration error 滴定误差titration index 滴定指数titration jump 滴定突跃titrimetry 滴定分析trace analysis 痕量分析transition interval 变色间隔transmittance 透射比tri acid 三元酸true value 真值tungsten lamp 钨灯ultratrace analysis 超痕量分析UV-VIS spectrophotometry 紫外-可见分光光度法volatilization 挥发Volhard method 福尔哈德法volumetric flask 容量瓶volumetry 容量分析Wash bottle 洗瓶washings 洗液water bath 水浴weighing bottle 称量瓶weighting form 称量形weights 砝码working curve 工作曲线xylenol orange (XO) 二甲酚橙zero level 零水平异步处理dispatch_async(dispatch_get_glo bal_queue(0, 0), ^{// 处理耗时操作的代码块... [self test1];//通知主线程刷新dispatch_async(dispatch_get_mai n_queue(), ^{//或者说是通知主线程刷新,NSLog(............);});。

医药行业专业英语词汇

医药行业专业英语词汇

医药行业专业英语词汇(非常有用)FDA和EDQM术语: CLINICAL?TRIAL:临床试验? ANIMAL?TRIAL:动物试验? ACCELERATED?APPROVAL:加速批准? STANDARD?DRUG:标准药物? INVESTIGATOR:研究人员;调研人员PREPARING?AND?SUBMITTING:起草和申报? SUBMISSION:申报;递交? BENIFIT (S):受益? RISK(S):受害? DRUG?PRODUCT:药物产品? DRUG?SUBSTANCE:原料药? ESTABLISHED?NAME:确定的名称? GENERIC?NAME:非专利名称? PROPRIETARY?NAME:专有名称;? INN(INTERNATIONAL?NONPROPRIETARY?NAME):国际非专有名称? ADVERSE?EFFECT:副作用? ADVERSE?REACTION:不良反应? PROTOCOL:方案? ARCHIVAL?COPY:存档用副本? REVIEW?COPY:审查用副本? OFFICIAL?COMPENDIUM:法定药典(主要指USP、?NF).? USP (THE?UNITED?STATES?PHARMACOPEIA):美国药典NF(NATIONAL?FORMULARY):(美国)国家处方集? OFFICIAL=PHARMACOPEIAL=?COMPENDIAL:药典的;法定的;官方的? AGENCY:审理部门(指FDA)? IDENTITY:真伪;鉴别;特性? STRENGTH:规格;规格含量(每一剂量单位所含有效成分的量)? LABELED?AMOUNT:标示量? REGULATORY?SPECIFICATION:质量管理规格标准(NDA提供)? REGULATORY?METHODOLOGY:质量管理方法? REGULATORY?METHODS?VALIDATION:管理用分析方法的验证COS/CEP?欧洲药典符合性认证ICH(International?Conference?on?Harmonization?of?Technical?Requirements?for?Registration?of PharmaceuticalsforHumanUse)人用药物注册技术要求国际协调会议ICH文件分为质量、安全性、有效性和综合学科4类。

大学英语专业写作5-comparison and contrast

大学英语专业写作5-comparison and contrast

• The business of a comparison and contrast essay is frequently (but not always) to demonstrate a preference for one thing over another. • The trick is to allow the preference to grow out of the comparison without actually stating the obvious. Let the reader figure out the preference from the language we use in the contrast; let the language do its work.
• Practice: • My hometown --- Old and New
Before 1980 population streets dirty, narrow, twisting, squares, broad, bikes parallel, bridges, cars old, small, crowded paper-making, Tall, spacious beer-making, printing, furniture Now
• Comparison and contrast are ways of looking at objects and thinking about how they are alike and different. • For instance, all of these items are alike because they are kinds of food, but there are many ways that they are different. They belong to different food groups. Some must be cooked before eating, and some can be eaten raw. • When you write comparison and contrast, you will pay attention to these kinds of details.

Effects of pH and salt concentration

Effects of pH and salt concentration

Effects of pH and Salt Concentration on Oil-in-Water Emulsions Stabilized Solely by Nanocomposite Microgel ParticlesBernard P.Binks,*,†Ryo Murakami,†Steven P.Armes,‡and Syuji Fujii‡Surfactant&Colloid Group,Department of Chemistry,Uni V ersity of Hull,Hull HU67RX,and Department of Chemistry,Dainton Building,Uni V ersity of Sheffield,Sheffield S37HF,United KingdomRecei V ed No V ember9,2005.In Final Form:January3,2006Aqueous dispersions of lightly cross-linked poly(4-vinylpyridine)/silica nanocomposite microgel particles are used as a sole emulsifier of methyl myristate and water(1:1by volume)at various pH values and salt concentrations at 20°C.These particles become swollen at low pH with the hydrodynamic diameter increasing from250nm at pH 8.8to630nm at pH2.7.For batch emulsions prepared at pH3.4,oil-in-water(o/w)emulsions are formed that are stable to coalescence but exhibit creaming.Below pH3.3,however,these emulsions are very unstable to coalescence and rapid phase separation occurs just after homogenization(pH-dependent).The pH for50%ionization of the pyridine groups in the particles in the bulk(p K a)was determined to be3.4by acid titration measurements of the aqueous dispersion.Thus,the charged swollen particles no longer adsorb at the oil-water interface.For continuous emulsions (prepared at high pH with the pH then decreased abruptly or progressively),demulsification takes place rapidly below pH3.3,implying that particles adsorbed at the oil-water interface can become charged(protonated)and detached from the interface in situ(pH-responsive).Furthermore,at a fixed pH of4.0,addition of sodium chloride to the aqueous dispersion increases the degree of ionization of the particles and batch emulsions are significantly unstable to coalescence at a salt concentration of0.24mol kg-1.The degree of ionization of such microgel particles is a critical factor in controlling the coalescence stability of o/w emulsions stabilized by them.IntroductionRecently there has been growing interest in emulsions stabilized by colloidal particles,so-called Pickering emulsions.1-3The energy of attachment of a single particle of intermediate wettability at the oil-water interface can be very high relative to the thermal energy kT,so particles once at the interface can be considered as effectively irreversibly adsorbed.4The effectiveness of the particulate emulsifier depends on the particle wettability,particle size,particle shape,particle concentration,and interparticle interactions.1,2These particulate emulsifiers offer a number of potential advantages over conventional surfactants such as imparting improved stability against coalescence and a reduced rate and extent of creaming/sedimentation owing to the enhanced viscosity of the continuous phase.1,2Inorganic particles such as silica,carbon black,barium sulfate,and calcium carbonate have been widely used as particulate emulsifiers.5However,the use of organic latex particles is much less common.Recently,tailor-made sterically stabilized polystyrene latex particles were synthesized and used to stabilize emulsions of oil and water.6-9 The tertiary amine methacrylate-based steric stabilizer was designed to be stimulus-responsive;the wettability of the particle at the oil-water interface can be changed by tuning the tem-perature,pH,or salt concentration.Temperature-induced phase inversion from oil-in-water(o/w)to water-in-oil(w/o)emulsions with increasing temperature6and demulsification of o/w emul-sions in situ with decreasing pH9can be realized.In principle,certain types of microgel particles could also act as a stimulus-responsive particulate emulsifier.Such particles comprise a cross-linked latex which is swollen in a good solvent.10-12In an aqueous medium,the transition between swollen and nonswollen particles can be triggered by adjusting the dispersion temperature,pH,or salt concentration.Poly(N-isopropylacrylamide),PNIPAM,is the most widely studied polymer for the preparation of temperature-sensitive microgel particles.10-12pH-sensitive microgel particles usually comprise either a weak polybase,e.g.,poly(4-vinylpyridine)or poly(2-vinylpyridine),or a weak polyacid,e.g.,poly(acrylic acid)or poly(methacrylic acid),which is often copolymerized with NIPAM or styrene.13-19These microgel particles are swollen either below(polybase)or above(polyacid)the p K a of the ionizable groups.We are aware of only two literature examples in which microgel particles act as a particulate emulsifier.Ngai et al.synthesized PNIPAM-stat-poly(methacrylic acid)copolymer microgel par-ticles cross-linked with N,N′-methylenebisacrylamide.20The microgel particles were swollen by either lowering the temperature or increasing the pH of the aqueous dispersion.At high pH,both*To whom correspondence should be addressed.E-mail: b.p.binks@ (B.P.B.).†University of Hull.‡University of Sheffield.(1)Binks,B.P.Curr.Opin.Colloid Interface Sci.2002,7,21.(2)Aveyard,R.;Binks,B.P.;Clint,J.H.Ad V.Colloid Interface Sci.2003, 100-102,503.(3)Tambe,D.E.;Sharma,M.M.Ad V.Colloid Interface Sci.1994,52,1.(4)Binks,B.P.;Lumsdon,ngmuir2000,16,8622.(5)Binks,B.P.;Lumsdon,ngmuir2000,16,2539.(6)Binks,B.P.;Murakami,R.;Armes,S.P.;Fujii,S.Angew.Chem.,Int.Ed. 2005,44,4795.(7)Amalvy,J.I.;Armes,S.P.;Binks,B.P.;Rodrigues,J.A.;Unali,G.-F. mun.2003,1826.(8)(a)Amalvy,J.I.;Unali,G.-F.;Li,Y.;Granger-Bevan,S.;Armes,S.P.; Binks,B.P.;Rodrigues,J.A.;Whitby,ngmuir2004,20,4345.(b)Read, E.S.;Fujii,S.;Amalvy,J.I.;Randall,D.P.;Armes,ngmuir2004,20, 7422.(9)Fujii,S.;Randall,D.P.Armes,ngmuir2004,20,11329.(10)Murray,M.J.;Snowden,M.J.Ad V.Colloid Interface Sci.1995,54,73.(11)Saunders,B.R.;Vincent,B.Ad V.Colloid Interface Sci.1999,80,1.(12)Pelton,R.Ad V.Colloid Interface Sci.2000,85,1.(13)Ferna´ndez-Nieves,A.;Ferna´ndez-Barbero,A.;Vincent,B.;de las Nieves,ngmuir2001,17,1841.(14)Kim,K.S.;Vincent,B.Polym.J.2005,37,565.(15)Kratz,K.;Hellweg,T.;Eimer,W.Colloids Surf.,A2000,170,137.(16)Pinkrah,V.T.;Snowden,M.J.;Mitchell,J.C.;Seidel,J.;Chowdhry,B. Z.;Fern,ngmuir2003,19,585.(17)Hoare,T.;Pelton,ngmuir2004,20,2123.(18)Loxley,A.;Vincent,B.Colloid Polym.Sci.1997,275,1108.(19)Rooney,M.T.V.;Seitz,mun.1999,36,267.(20)Ngai,T.;Behrens,S.H.;Auweter,mun.2005,331.2050Langmuir2006,22,2050-205710.1021/la053017+CCC:$33.50©2006American Chemical SocietyPublished on Web01/31/2006swollen particles at25°C and nonswollen ones at60°C act as an efficient emulsifier for o/w emulsions.However,no stable emulsions could be obtained at pH2,irrespective of the temperature.In our recent paper,Fujii et al.described the synthesis of poly(4-vinylpyridine)/silica,P4VP/SiO2,nanocomposite mi-crogel particles and their use as a pH-responsive particulate emulsifier of water and several oils.21At high pH(8-9),the emulsions were stable to coalescence but exhibited creaming/ sedimentation.o/w emulsions were formed with methyl myristate and n-dodecane,whereas a w/o emulsion was preferred with 1-undecanol.In contrast,these nanocomposite microgel particles proved to be ineffective emulsifiers at pH2-3,with macroscopic phase separation occurring immediately after emulsion formation. Thus,these particles exhibit pH-dependent emulsification. Furthermore,the addition of HCl to a methyl myristate-in-water emulsion originally prepared at pH8-9caused rapid and complete demulsification in situ.Thus,these particles also exhibit pH-responsive behavior.The main aim of this study is to explore in more detail the behavior of both the pH-dependent and pH-responsive emulsions of methyl myristate in water identified in ref21,and determine the critical pH required for their demulsification by employing three different emulsification protocols.The properties of these emulsions are elucidated using conductivity,optical microscopy, and light diffraction measurements and are correlated with the known properties of the nanocomposite microgel particles in aqueous solution in the absence of oil.Ionizable colloidal particles in water are significantly affected by the addition of salt,22-24 since the presence of salt affects the degree of ionization.We have therefore also investigated the effect of salt concentration, at fixed pH,on both the aqueous dispersions and the emulsions prepared from them to understand more fully the impact of particle ionization on emulsifier efficiency.Experimental SectionMaterials.P4VP/SiO2nanocomposite microgel particles were prepared by statistical copolymerization of4-vinylpyridine with a bifunctional cross-linker in the presence of an ultrafine(20nm diameter)hydrophilic silica sol in an aqueous medium.21Ammonium persulfate and ethylene glycol dimethacrylate(EGDMA)were employed as the free radical initiator and cross-linker,respectively. The particles were lightly cross-linked;1.0wt%EGDMA was employed on the basis of the amount of4-vinylpyridine monomer. Cross-linking of P4VP with EGDMA is essential to prevent the P4VP chains from dissolving at low pH.25Details of the synthesis have been reported elsewhere.21The milky white dispersion of P4VP/ SiO2particles obtained was carefully purified by centrifugation-redispersion cycles,with each successive supernatant being decanted and replaced with doubly distilled water until no excess silica sol remained,as observed by transmission electron microscopy.Ther-mogravimetric analysis indicated a mean silica content of ap-proximately35wt%,which is consistent with the silica content reported for the non-cross-linked P4VP/SiO2microgel particles.21,25 This fact suggests that the lightly cross-linked microgel particles should have the so-called“currant bun”particle morphology that confers dual surface character at or above neutral pH,i.e.,segregated nanodomains of hydrophilic silica and hydrophobic P4VP chains.26-30All water used in this study was first passed through an Elga reverse osmosis unit and then through a Milli-Q reagent water system. Methyl myristate(99%,Aldrich)was used as the oil and was columned twice through basic aluminum oxide.Hydrochloric acid (AR grade,Fisher Scientific)used for adjusting the pH and sodium chloride(AnalaR,BDH)were used without further purification. Methods.Preparation of Aqueous Dispersions of Microgel Particles.(i)Aqueous Dispersions of Particles at Various pH Values in the Absence of Added Salt.An aqueous dispersion(1.0wt%)of P4VP/SiO2microgel particles was prepared by diluting the original 7.96wt%aqueous dispersion,at pH8-9,using Milli-Q water.The pH was then lowered by adding a small volume of aqueous HCl. (ii)Aqueous Dispersions of Particles at pH4.0in the Presence of Salt.Solid NaCl was placed in a glass vessel,and approximately 5mL of a1.0wt%aqueous dispersion of P4VP/SiO2microgel particles was added.The mixture was stirred with a magnetic stirrer for1h.The pH of the mixture was adjusted to4.0using aqueous HCl,and the mixture was stirred for a further hour.All preparations were carried out at room temperature.Characterization of Aqueous Dispersions of Microgel Particles. To determine the p K a value of the P4VP/SiO2particles,5.0mL of the aqueous dispersion was titrated with aqueous HCl.The pH was monitored using a pH meter(Hydrus400,FisherBrand)equipped with a pH electrode(FB68791)at room temperature.Calibration was carried out using buffer solutions of pH4,7,and10.Dynamic light scattering of a1.0wt%aqueous microgel dispersion was carried out using a Malvern Nano ZS ZEN3600instrument under a N2atmosphere at a scattering angle of173°.Three measurements were made at each pH,with30min being allowed for equilibration. potentials were calculated from the measured electrophoretic mobilities determined using the Malvern Nano ZS ZEN3600 instrument.Measurements were averaged over20runs using dilute dispersions(0.01wt%)at different pH values.The dispersion was diluted with aqueous Na2SO4to provide a suitable background electrolyte concentration to minimize electrical double layer effects. The measurements were carried out at20°C.Preparation of Emulsions.In this study we employed three different emulsification protocols.(i)Protocol1(Batch Emulsion).Equal volumes(5.0mL)of oil and aqueous dispersion at different pH values or salt concentrations were placed in a glass vessel(inner volume14mL)at room temperature.The two phases were kept in a thermostated bath at20°C and then homogenized at13000rpm for2min with an Ultra Turrax T25homogenizer(1cm head)at20°C.(ii)Protocol2(Continuous Emulsion with pH Changes after Homogenization).Equal volumes(32mL)of methyl myristate and 1wt%aqueous dispersion at pH8.1were placed in a glass vessel (inner volume120mL)at room temperature.The two phases were kept in a thermostated bath at20°C and then homogenized at13000 rpm for4min(twice as long due to the increased volume)with an Ultra Turrax T25homogenizer(1cm head)at20°C.The emulsion was subdivided into glass vessels of8mL each whose pH was individually adjusted rapidly by addition of a small volume of aqueous HCl to the continuous phase.(iii)Protocol3(Continuous Emulsion).Equal volumes(5.0mL) of oil and1wt%aqueous dispersion at pH8.1were placed in a glass vessel(inner volume14mL)at room temperature.The two phases were kept in a thermostated bath at20°C and then homogenized at13000rpm for2min with an Ultra Turrax T25 homogenizer(1cm head)at20°C.The pH of the emulsion immediately after preparation was7.5and was progressively lowered by adding a small volume of aqueous HCl with gentle shaking. Characterization of Emulsions.The emulsion type was inferred by observing whether a drop of the emulsion dispersed when added to a small volume of water or oil.The stabilities of emulsions at20(21)Fujii,S.;Read,E.S.;Binks B.P.;Armes,S.P.Ad V.Mater.2005,17, 1014.(22)Stone-Masui,J.;Watillion,A.J.Colloid Interface Sci.1975,52,479.(23)Schulz,S.F.;Gisler,T.;Borkovec,M.;Sticher,H.J.Colloid Interface Sci.1975,52,479.(24)Binks,B.P.;Rodrigues,J.A.Angew.Chem.,Int.Ed.2005,44,441.(25)Fujii,S.;Blanazs,A.;Read,E.S.;Armes,S.P.;Binks B.P.;Murakami, ngmuir,to be submitted for publication.(26)Barthet,C.;Hickey,A.J.;Cairns,D.B.;Armes,S.P.Ad V.Mater.1999, 11,408.(27)Percy,M.J.;Amalvy,J.I.;Barthet,C.;Armes,S.P.;Greaves,S.J.; Watts,J.F.;Wiese,H.J.Mater.Chem.2002,12,697.(28)Percy,M.J.;Barthet,C.;Lobb,J.C.;Khan,M.A.;Lascelles,S.F.; Vamvakaki,M.;Armes,ngmuir2000,16,6913.(29)Agarwal,G.K.;Titman,J.J.;Percy,M.J.;Armes,S.P.J.Phys.Chem. B2003,107,12497.(30)Amalvy,J.I.;Percy,M.J.;Armes,S.P.;Leite,C.A.P.;Galembeck,F. Langmuir2005,21,1175.pH and Salt Concentration Effects on o/w Emulsions Langmuir,Vol.22,No.5,20062051°C were assessed by monitoring the movement of the oil -emulsion and water -emulsion interfaces.For water-continuous emulsions,the upward movement of the water -emulsion boundary was used as a measure of the stability to creaming,and the position of the oil -emulsion interface was used as an indicator of coalescence.The conductivities of aqueous NaCl,aqueous dispersions,and emulsions were measured using a Jenway 4510conductivity meter with Pt/Pt black electrodes.The pH of an emulsion was monitored by a Hydrus 400pH meter (FisherBrand).Small samples of emulsion/dispersion were placed in a hemocytometer cell (Weber Scientific)and viewed with a Nikon Labophot microscope fitted with a QICAM 12-bit Mono Fast 1394camera (QImaging).Photographs of vials containing emulsions were taken with a Dimage Xg digital camera (Konica Minolta).All images were processed with Image-Pro Plus version 5.1software (Media Cybernetics).Volume-weighted droplet size distributions of o/w emulsions were measured using a Malvern MasterSizer 2000instrument at room temperature.The emulsion droplets were diluted in water at the same pH and NaCl concentration as those in the original aqueous dispersion and circulated through the dispersion unit.The optical unit was cleaned between samples by being rinsed with 2-propanol and pure water several times.At least two measurements were made on separate samples for each system.Results and DiscussionThe nanocomposite microgel particles used here become increasingly cationic upon lowering the pH of the aqueous dispersion.This is mainly due to protonation of the pyridine groups on the P4VP chains but also due in part to protonation of the anionic silanol groups on the surface of the silica sol.More importantly,the particles also become much more hydrophilic and swollen with water.It is worthwhile to consider the relationship between the pH of the aqueous dispersion and the degree of ionization of the polymerized pyridine groups in the particles.Let us consider the following equilibrium for 4VPand define the proton dissociation constant of a pyridine group K a asand the degree of ionization of a pyridine group R asCombining eqs 1and 2,we obtain the Henderson -Hasselbach equationorFigure 1shows the relationship between R and pH calculated on the basis of eq 4.It is found that the R value depends critically on the pH -p K a difference,especially when the values of pH and p K a lie close together.Since emulsion stability depends crucially on the wettability of the particles at the interface,1it was expected that the behavior of emulsions stabilized with these P4VP/SiO 2microgel particles would change drastically at pH values close to the p K a of the particles in the bulk aqueous dispersion.Aqueous Particle Dispersions.Effect of pH .Values of the potential and hydrodynamic diameter of the nanocompositemicrogel particles are plotted against the pH of the aqueous dispersion in Figure 2.These potential data show a classical “S”shape,being positive at low pH and negative at high pH.The isoelectric point of the particles is estimated to be around 6,which is practically identical to the value reported for non-cross-linked P4VP/SiO 2microgel particles.27The particles possess one cationic (pyridine)and two anionic (silanol and sulfate)ionizable surface groups.The sulfate groups,originating from the persulfate initiator,are ionized over a wide range of pH because the p K a values for sulfuric acid in water are -3and 2.31Similarly,the silica sols used to prepare these P4VP/SiO 2particles remain anionic over a wide range,displaying negative potentials ranging from -30mV at pH 2.5to -56mV at pH 9.1.27Hence,the P4VP/SiO 2particles are anionic at high pH owing to their ionized silanol and sulfate groups,but become cationic at low pH due to protonation of the pyridine groups.The hydrodynamic diameter of the nonprotonated “hard”sphere microgel particle is almost constant (at about 250nm)at pH >8.At around pH 3.4(which corresponds approximately to the p K a value of the P4VP chains;see later),the diameter increases dramatically with decreasing pH.This is attributed to swelling of the cationic microgel particles with water.Just either side of their isoelectric-C 5H 4NH +T -C 5H 4N +H +K a ){[-C 5H 4N][H +]}/[-C 5H 4NH +](1)R )[-C 5H 4NH +]/{[-C 5H 4N]+[-C 5H 4NH +]}(2)pH -p K a )log[(1-R )/R ](3)R )1/(1+10pH -p K a )(4)Figure 1.Degree of ionization of basic groups,e.g.,pyridine,versus pH -p K a calculated using eq4.Figure 2. potential (4)and hydrodynamic diameter (9)of P4VP/SiO 2microgel particles versus pH for an aqueous dispersion at 20°C in the absence of salt.The dotted line indicates a p K a of 3.4.At each pH,three measurements of size were made,standard deviation 10nm.2052Langmuir,Vol.22,No.5,2006Binks et al.point (pH 6),the microgel particles are too flocculated to allow estimation of their primary diameter.Figure 3shows optical microscopy images of 1.0wt %aqueous dispersions at different pH values.At pH 7.5(d),there is no significant observable matter because the discrete particles are too small (about 250nm).Highly flocculated particles are observed around the isoelectric point (c)as expected.On lowering the pH further,slightly cationic particles remain weakly flocculated (b).Because the particles are highly cationic and swollen below their p K a value of 3.4(a),they are barely visible since the refractive index difference between the aqueous medium and the microgel particles is very small.18,19Effect of Salt Concentration .Figure 4shows the titration curves of 5.0mL of 1.0wt %aqueous dispersions of the P4VP/SiO 2particles at various molalities of NaCl (m NaCl )using HCl.In all cases,an inflection point can be observed as the pyridine groupsbecome protonated on addition of acid.The pH value obtained for a given amount of HCl increases with increasing m NaCl .The p K a value for each curve was estimated by determining the slopes of the different parts of the curve and estimating the pH at which the slope is a minimum.In Figure 5a the dependence of the p K a on m NaCl is shown.At m NaCl )0,the p K a is 3.4,but addition of NaCl increases this value.It is expected that the particles are nonswollen above the p K a vs m NaCl curve while cationic and swollen below it.Furthermore,the degree of ionization of the P4VP chains in the particles as a function of m NaCl at a fixed pH 4can be evaluated using eq 4and the p K a values given in Figure 5a.As seen in Figure 5b,addition of salt enhances ionization due to screening of the charges;R increases sharply from a value of ∼0.2at m NaCl )0to more than 0.8at 0.05mol kg -1NaCl.It has been reported that microgel particles con-taining ionizable groups become deswollen in the presence of salt because an increase in ionic strength decreases the Debye screening length and hence reduces the repulsive electrostatic forces between charged groups.14,15However,our light scat-tering measurements gave a hydrodynamic diameter of the microgel particles of 700nm at pH 4.0and m NaCl )0.2mol kg -1,compared with ∼300nm in the absence of salt.In addition,microscopy observations showed that at this pH particles are flocculated in the absence of salt,Figure 3e,but barely visible and hence probably swollen at m NaCl )0.24mol kg -1,Figure 3f.Therefore,the P4VP chains are cationic and swollen at low pH and high m NaCl .It is also noticed that the molality of NaCl corresponding to R )0.5is estimated to be 0.01mol kg -1at this pH.Emulsions of Oil and Water.Effect of pH .Figure 6shows the conductivities of 1.0wt %aqueous dispersions of the P4VP/SiO 2particles and also of the emulsions obtained from the homogenization of methyl myristate and an aqueous dispersion (1:1by volume)using protocol 1at different pH values.The conductivity of the aqueous dispersion monotonically increases on lowering the pH.At 3.4e pH e 8.9,the conductivity of the emulsion is much higher than that of pure methyl myristate and is comparable to that of the aqueous dispersion.In addition,drop tests indicated that these emulsions were water-continuous.Thus,o/w emulsions are obtained at all pH values.However,at pH 3.3,complete phase separation of the emulsion was observed less than 3min afterhomogenization.Figure 3.Optical micrographs of 1.0wt %aqueous dispersions of P4VP/SiO 2microgel particles at various solution pH values in the absence of salt:(a)3.0,(b)3.4,(c)5.5,(d)7.5,(e)4.0.(f)is for pH 4.0in the presence of 0.24mol kg -1NaCl.The scale bar is the same on eachmicrograph.Figure 4.Titration curves obtained for 1.0wt %aqueous dispersions of P4VP/SiO 2microgel particles using aqueous HCl at various NaCl concentrations:(1)0,(2)0.010,(3)0.020,(4)0.040,(5)0.060,(6)0.10,(7)0.14,(8)0.22,(9)0.26mol kg -1.Figure 5.(a)p K a of the P4VP/SiO 2microgel particles estimated from Figure 4against NaCl molality.(b)Estimated degree of ionization of pyridine groups in the P4VP/SiO 2microgel particles as a function of NaCl molality using eq 4and p K a values shown in (a)at pH 4.pH and Salt Concentration Effects on o/w Emulsions Langmuir,Vol.22,No.5,20062053The average drop diameter of o/w emulsions prepared using protocol 1immediately after homogenization is plotted against pH in Figure 7.At 4e pH e 8.9,a distinct shallow minimum occurs at around pH 5-6.This pH corresponds approximately to the isoelectric point,where the P4VP/SiO 2particles are known to be highly flocculated (Figure 3c).Thus,the flocculated particles appear to stabilize finer oil drops.Significant flocculation of the emulsion drops occurs at 3.4e pH <4(see later).If the flocs are stable to dilution,the apparent diameter measured is larger than that of individual drops.The close correspondence of the mean and median diameters reflects the unimodal log-normal size distributions in these samples.In Figure 8,optical micrographs of the emulsions prepared using protocol 1and diluted with water at the same pH as that of the aqueous dispersion are shown immediately after homog-enization.At relatively high pH (c,d),drops are discrete,spherical,and simple (not multiple).At 3.4e pH <4(b),drops are also spherical and simple but appear flocculated.Below pH 3.3(a),smaller drops are observed (the sample was taken from theaqueous phase after phase separation),although the emulsions rapidly phase separated.However,these drops disappeared from the aqueous phase within 24h.The long-term stability (after 6months)of o/w emulsions prepared using protocol 1is evaluated in terms of the fractions of resolved oil,f o ,due to coalescence and resolved water,f w ,due to creaming.In Figure 9a,the parameter f o (or f w )is defined as the volume of oil (or water)resolved relative to the initial volume of oil (or water).The emulsions at and above pH 3.4creamed to a similar extent at all pH values but were completely stable to coalescence.On the other hand,at pH 3.3,emulsions are very unstable to coalescence and complete phase separationoccurredFigure 6.Conductivities of a 1.0wt %aqueous dispersion of P4VP/SiO 2microgel particles and methyl myristate-in-water emulsions prepared from the dispersion using protocol 1immediately after preparation as a function of pH.The vertical dotted line indicates the boundary between stable and unstable emulsions (with respect tocoalescence).Figure 7.Average drop diameters of o/w emulsions as a function of pH for freshly prepared emulsions using protocol 1.Sizes determined using light diffraction (0,arithmetic mean diameter;9,median diameter)are shown.The standard deviation of the mean is in the range 3-5µm.The dashed line indicates the boundary between stable and unstableemulsions.Figure 8.Optical micrographs of o/w emulsions prepared using protocol 1immediately after preparation at various pH values of the 1.0wt %aqueous particle dispersion:(a)3.0,(b)3.4,(c)5.5,(d)7.5.The scale bar is the same on eachmicrograph.Figure 9.Long-term stability of o/w emulsions stored at 20°C:emulsions prepared using protocol 1(a)or protocol 2(b)after 6months and protocol 3(c)after 48h.All emulsions are of the o/w type.f o (4)relates to coalescence,and f w ([)relates to creaming.The dotted line indicates the boundary between stable and unstable emulsions.2054Langmuir,Vol.22,No.5,2006Binks et al.within3min of preparation.This distinct boundary between stable and unstable emulsions lies at around pH3.4.It can be recalled that the pH of this boundary is identical to the p K a of the particles in the bulk aqueous dispersion(Figure5a).Therefore, once particles become sufficiently ionized,they become more hydrophilic,swell,and no longer adsorb at the oil-water interface, leading to significant coalescence of bare oil drops.Parts b and c of Figure9show the stability of continuous emulsions prepared using protocols2and3,respectively.Here, the pH of the emulsion was monitored instead of that of the aqueous dispersion.Equating the pH of the dispersion with that of the emulsion is valid since the pH of emulsions prepared by protocol1was practically identical to that of the aqueous dispersions prior to homogenization.Although the microgel particles are already adsorbed in protocols2and3,an abrupt decrease in emulsion pH starting from around8is effected for protocol2whereas a progressive reduction occurs with protocol 3.However,there is no significant difference between the results using protocol2or3,so the demulsification is independent of the manner in which the emulsion pH is adjusted.In both protocols,demulsification again occurs rapidly below pH3.4, implying that the initially adsorbed particles become swollen cationic microgels and then detach from the oil-water interfaces in situ;i.e.,both the emulsifier and the emulsion are pH-responsive.The critical pH for demulsification of continuous emulsions prepared using protocols2and3is practically identical to the p K a value of the P4VP/SiO2particles in the aqueous dispersion. This behavior differs from that of hexadecane-in-water emulsions stabilized by poly[2-(dimethylamino)ethyl methacrylate-block-methyl methacrylate](PDMA-b-PMMA)-stabilized polystyrene particles,in which the emulsion prepared at high pH(8)was not significantly demulsified by adding HCl to the emulsion.8In both systems,a part of the particles is immersed in the oil phase. However,in the present system,the nanocomposite microgel particles can be swollen by water,and then the surface of the particles immersed in the oil phase as well as the core can be protonated by lowering the pH.It is suggested that the difference in the demulsification behavior between the PV4P/SiO2microgel particle system and the PDMA-b-PMMA-stabilized polystyrene particle system is due to the difficulty of achieving high degrees of protonation of PDMA groups in the oil phase.21Effect of Salt Concentration.In the absence of salt,all emulsions prepared below the p K a of the particles,i.e.,above R)0.5,were very unstable and rapidly phase separated.On the other hand, the addition of salt increases the p K a value,and the degree of ionization at a fixed pH is also increased.It was therefore expected that the P4VP/SiO2particles would become more charged and hydrophilic in the presence of added NaCl,leading to coalescence instability of the emulsions.Figure10shows the conductivities of a1.0wt%aqueous dispersion of P4VP/SiO2particles and the corresponding methyl myristate-in-water emulsion plotted against m NaCl at pH4.The conductivity of an aqueous NaCl solution alone is included as a reference.The conductivity of the aqueous dispersion increases with increasing m NaCl and is practically identical to that of the aqueous NaCl solution,implying that at this pH the particles make a negligible contribution to the measured conductivity.At m NaCl)0.20mol kg-1,the conductivity of the emulsion is much larger than that of methyl myristate and is approximately half that of the aqueous dispersion due to the obstruction effect of the oil drops.In addition,drop tests confirmed the existence of o/w emulsions at all m NaCl values.At m NaCl)0.22mol kg-1it was not possible to measure the conductivity of the emulsion due to the significant coalescence which occurred at this m NaCl. At m NaCl)0.24mol kg-1rapid phase separation occurred within 3min of homogenization,as expected.The mean diameter of drops in the o/w emulsions immediately after preparation is plotted against m NaCl in Figure11.This graph can be divided into three regions:below0.055mol kg-1,between 0.055and0.23mol kg-1,and above0.23mol kg-1,corresponding to emulsions that are stable to coalescence,emulsions increasingly unstable to coalescence,and complete phase separation,respec-tively.The smallest drop diameters of30µm appear in the first region where emulsions are flocculated by low salt concentration (see later).These values reflect those of the flocs rather than discrete drops.In the light scattering measurements,emulsions were diluted and sheared in the dispersion unit.However,after the measurement,both discrete and flocculated oil drops were observed;the diameters of the flocs ranged from20to50µm as judged by optical microscopy.Above0.05mol kg-1,the mean drop diameter increases gradually with increasing m NaCl as a result of coalescence and reaches an average diameter of160µm,after which stable emulsions cannot be prepared. Optical micrographs of fresh emulsions diluted with water at pH4using the same m NaCl as that for the aqueous dispersionare Figure10.Conductivity versus NaCl molality at20°C:(2)1.0 wt%aqueous dispersion at pH4.0,(4)aqueous NaCl at pH4.0, (9)o/w emulsion at pH4.0.Figure11.Drop diameter of o/w emulsions versus NaCl molality in the aqueous dispersion for batch emulsions of equal volumes of methyl myristate and a1.0wt%aqueous dispersion of P4VP/SiO2 microgel particles at pH4.Sizes were determined by light diffraction (0,arithmetic mean diameter;9,median diameter).The error bar for the mean was estimated from the standard deviation of two sets of data.pH and Salt Concentration Effects on o/w Emulsions Langmuir,Vol.22,No.5,20062055。

药物分析报告常用英语词汇

药物分析报告常用英语词汇

药物分析专业英语词汇表Aabsorbance 吸收度 absorbance ratio 吸收度比值absorption 吸收 absorption curve 吸收曲线absorption coefficient 吸收系数 accurate value 准确值Acid—dye colormcty 酸性染料比色法 acidimcty 酸量法acidity 酸度 activity 活度adjusted retention time 调整保留时间 absorbent 吸收剂absorption吸附 alkalinity 碱度alumina 氧化铝,矾土 ambient temperature 室温ammonium thiocyanate 硫氰酸铵 analytical quality control 分析质量控制 anhydrous substance 干燥品antioxidant 抗氧剂 application of sample 点样area normalization method 面积归一法 arsenic 砷arsenic sport 砷斑 assay 含量测定assay tolerance 含量限度 attenuation 衰减acid burette 酸式滴定管 alkali burette 碱式滴定管a mortar 研钵Bback extraction 反萃取 band absorption 谱带吸收batch 批 batch number 批号Benttendorlf method 白田道夫法 between day precision 日间密度精biotransformation 生物转化 blank test 空白试验boiling range 沸程 British Pharmacopeia 英国药典bromate titration 溴酸盐滴定法 bromine method 溴量法bromothymol blue 溴麝香酚蓝bulk drug 原料药by—product 副产物breaker 烧杯burette glass bead nozzle 滴定管 brown acid burette 棕色酸式滴定管Ccalibration curve 校正曲线 calomel electrode 甘汞电极calorimetry 量热分析 capacity factor 容量因子capillary gas chromatography 毛细管气相色谱法carrier gas 载气characteristics description 性状chelate compound 螯合物 chemical equivalent 化学当量Chinese pharmacopeia 中国药典 Chinese material medicine 中成药Chinese material midical preparation 中药制剂 chiral 手性的chiral carbon atom 手性碳原子 chromatogram 色谱图chromatography 色谱法 chromatographic column 色谱柱chromatographic condition 色谱条件 clarity 澄清度coefficient of distribution 分配系数 coefficient of variation 变异系数color change interval 变色范围 color reaction 显色反应colormetry 比色法 column efficiency 柱效column temperature 柱温 comparative test 比较试验completeness of solution 溶液的澄清度 conjugate 缀合物concentration—time curve 浓度时间曲线 confidence interval 置信区间confidence level 置信水平 controlled trial 对照试验correlation coefficient 相关系数 contrast test 对照试验congealing point 凝点 content unifarmity装量差异controlled trial 对照试验 correlation coefficient 相关系数contrast test 对照试验 counter ion 反离子cresal red 甲酚红 cuvette cell 比色池cyanide氰化物 casserole small 勺皿Ddead—stop titration 永定滴定法 dead time 死时间deflection 偏差 deflection point 拐点degassing 脱气 deionized water 去离子水deliquescence 潮解 depressor substances test 降压物质检查法 desiccant 干燥剂detection 检查 developing reagent 展开剂developing chamber 展开室 deviation 偏差dextrose 右旋糖 diastereoisomer 非对映异构体diazotization 重氮化 differential thermal analysis 差示热分析法 differential scanning calorimetry 差示扫描热法Gutzeit 古蔡 day to day precision 日间精密度dissolution 溶出度direct injection 直接进样 2,6-dichlorindophenol titration 2,6-二氯靛酚滴定法 digestion 消化diphastic titration 双向滴定 disintegration test 崩解试验dispersion 分散度 dissolubility 溶解度dissolution test 溶解度检查 distilling range 滴程distribution chromatography 分配色谱 dose 剂量drug quality control 药品质量控制 drying to constant weight 干燥至恒重duplicate test 重复试验disk method water method 压片法Eeffective constituent 有效成分 effective plate number 有效板数 effective of column 柱效electrophoresis 电泳 elimination消除eluate 洗脱液 elution 洗脱enamtiomer 对映体 end absorption 末端吸收endogenous substances 内源性物质 enzyme drug 酶类药物enzyme induction 酶诱导 enzyme inhibition 酶抑制epimer 差向异构体 equilibrium constant 平衡常数error in volumetric analysis 容量分析误差exclusion chromatography 排阻色谱法 expiration date 失效期external standard method 外标法 extract 提取物extration gravimetry 提取重量法 extraction titration 提取容量法 extrapolated method外插法Erlenmeyer flask 锥形瓶 evaporating dish small 蒸发皿elongated bulb 胖肚 electronic balance MettlerAL204 MettlerAL204电子天平Ffactor 系数 fehling’s reaction 斐林实验filter 过滤 fineness of the particles 颗粒细度flow rate 流速fluorescent agent 荧光剂 fluorescence spectrophotometry 荧光分光光度法fluorescence detection 荧光检测器fluorescence analysis 荧光分析法foreign pigment 有色杂质formulary 处方集 free 游离freezing test 冻结试验 fused silica 熔融石英filter paper 滤纸Ggas chromatography 气相色谱法 gas-liquid chromatography 气液色谱法 gas purifier 气体净化器General identification test 一般鉴别试验 general notices凡例General requirements (药典) 通则 good clinical practices 药品临床管理规范 good laboratory practices 药品实验室管理规范 good manufacturing practices(GMP) 药品生产质量管理规范good supply practices(GSP) 药品供应管理规范 gradient elution 梯度洗脱grating 光栅 gravimetric method 重量法Gutzeit test 古蔡(检砷)法 glass funnel long stem 玻璃漏斗grad cylinder 量筒 glass rod 玻棒graduated pipettes 刻度吸管 GC 气相色谱Hheavy metal 重金属 half peak width 平峰宽heat conductivity 热导率height equivalent to atheoretical plate 理论塔板高度 height of an effective plate有效塔板高度high-performance liquid chromatography (HPLC)高效液相色谱法high-performance thin-layer chromatography (HPTLC)高效薄层色谱法hydrate 水合物 hydrolysis 水解hydrophilicity 亲水性 hydrophobicity 疏水性hydroxyl value 羟值 hyperchromic effect 浓色效应hypochromic effect 淡色效应 HHS-type constant temperature waterbath HHS型恒温水锅 HPLC 高效液相色谱法Iidentification 鉴别 ignition to constant weight 灼烧至恒重 immobile phase 固定相immunoassay 免疫测定 impurity 杂质inactivation 失活 index 索引indicator electrode 指示电极 indicator 指示剂inhibitor 抑制剂 injecting septum 进样隔膜胶垫instrumental analysis 仪器分析 injection value 进样阀insulin assay 胰岛素生物检测法 integrator 积分仪intercept 截距 interface 接口internal standard substance 内标物质 International unit 国际单位in vitro 体外 in vivo 体内iodide 碘化物 iodoform reation 碘仿反应iodometry 碘量法ion pair chromatography 离子对色谱 ion suppression 离子抑制ion suppression 离子抑制 ionic strength 离子强度ion-pairing agent 离子对试剂 ionization 电离isoabsorptive point 等吸收点 isocratic elution 等溶剂组成洗脱 isoelectric point 等电点isoosmotic solution 等渗溶液irreversible indicator 不可逆指示剂irreversible potential 不可逆电位KKarl Fischer titration 卡尔-费舍尔滴定Kjeldahl method for nitrogen 凯氏定氮法 Kober reagent 科伯试剂Kovats retention index 科瓦茨保留指数Llabelled amount 标示量 leading peak 前延峰leveling effect 均化效应 licensed pharmacist 执业药师 limit control 限量控制limit of detection 检测限 limit of quantitation 定量限 limit test 杂质限度试验loss on drying 干燥失重 low pressure gradient pump 氧压梯度泵 linearity and range 线性及范围linearity scanning 线性扫描 luminescence 发光litmus paper 石蕊试纸 lyophilization 冷冻干燥Mmain constituent 主成分 make-up gas 尾吹气maltol reaction 麦芽酚试验 Marquis test 马奎斯试验mass analyzer detector 质量分析检测器 mass spectrometric analysis 质谱分析 mass spectrum 质谱图mean deviation 平均偏差 melting point 熔点melting range 熔距 metabolite 代谢物metastable ion 亚稳离子 micellar chromatography 胶束色谱法 microanalysis 微量分析microcrystal 微晶 microdialysis 微透析migration time 迁移时间 Millipore filtration 微孔过滤 mobile phase 流动相molecular formula 分子式 monitor 检测monochromator 单色器 monographs 正文Nnatural product 天然产物 Nessler’s reagent 碱性碘化汞试液 neutralization 中和nitrogen content 总氮量nonaqueous acid-base titration 非水酸碱滴定 nonprescription drug ,over the counter drugs 非处方药 nonspecific impurity 一般杂质non-volatile matter 不挥发物 normal phase 正相normalization 归一化法 Nessler color comparison tube 纳氏比色管Onotice 凡例 octadecyl silane bonded silicagel 十八烷基硅烷键合硅胶 odorless 辛基硅烷odorless 无臭 official name 法定名official test 法定试验 on-column detector 柱上检测器on-column injection 柱头进样 on the dried basis 按干燥品计opalescence 乳浊 optical activity 光学活性optical isomerism 旋光异构 optical purity 光学纯度organic volatile impurities 有机挥发性杂质 orthogonal test 正交试验orthophenanthroline 邻二氮菲 outlier 可疑数据overtones 倍频封 oxidation-reduction titration 氧化还原滴定oxygen flask combustion 氧瓶燃烧Ppacked column 填充柱 packing material 色谱柱填料palladium ion colorimetry 钯离子比色法 parent ion 母离子particulate matter 不溶性微粒 partition coefficient 分配系数pattern recognition(ppm)百万分之几 peak symmetry 峰不对称性peak valley 峰谷 peak width at half height 半峰宽percent transmittance 透光百分率pH indicator absorbance ratio method pH指示剂吸光度比值法pharmaceutical analysis 药物分析 pharmacopeia 药典pharmacy 药学 photometer 光度计polarimetry 旋光测定法 polarity 极性polydextran gel 葡聚糖凝胶 potentiometer 电位计potentiometric titration 电位滴定法 precipitation form 沉淀形式precision 精密度 preparation 制剂prescription drug 处方药 pretreatment 预处理primary standard 基准物质 principal component analysis 主成分分析prototype drug 原型药物 purification 纯化purity 纯度 pyrogen 热原pycnometer method 比重瓶法 plastic wash bottle 洗瓶platform balance 天平 pipette 移液管pyknowmeter flasks 容量瓶Qquality control 质量控制 quality evaluation 质量评价quality standard 质量标准 quantitative determination 定量测定quantitative analysis 定量分析 quasi-molecular ion 准分子离子Rracemization 消旋化 random sampling 随机抽样rational use of drug 合理用药 readily carbonizable substance 易炭化物质 reagent sprayer 试剂喷雾剂recovery 回收率 reference electrode 参比电极related substance 相关物质 relative density 相对密度relative intensity 相对强度 repeatability 重复性replicate determination 平行测定 reproducibility 重现性residual basic hydrolysis method 剩余碱水解法residual liquid junction potential 残余液接电位residual titration 剩余滴定 residuce on ignition 炽灼残渣resolution 分辨率 response time 响应时间retention 保留 reversed phase chromatography 反相色谱法reverse osmosis 反渗透 rinse 淋洗robustness 可靠性 round 修约reagent bottles 试剂瓶 round bottom flask 圆底烧瓶rubber suction bulb 洗耳球Ssafety 安全性 Sakaguchi test 坂口试验salt bridge 盐桥 salting out 盐析sample applicator 点样器 sample application 点样sampling 取样 saponification value 皂化值saturated calomel electrode 饱和甘汞电极 selectivity 选择性significant difference 显著性水平 significant testing 显著性检验silica get 硅胶 silver chloride electrode 氯化银电极similarity 相似性 sodium dodecylsulfate 十二基酸钠solid-phase extraction 固相萃取 solubility 溶解度specific absorbance 吸收系数 specification 规格specificity 专属性 specific rotation 比旋度specific weight 比重 spiked 加入标准的split injection 分流进样 spray reagent 显色剂stability 稳定性 standard color solution 标准比色液standard deviation 标准差 standardization 标定standard substance 标准品 statistical error 统计误差sterility test 无菌试验 stock solution 储备液stoichiometric point 化学计量点 storage 贮藏stray light 杂散光 substrate 底物substituent 取代基 sulfate 硫酸盐sulphated ash 硫酸盐灰分 support 载体suspension 旋浊度 swelling degree 膨胀度symmetry factor 对称因子 systematic error 系统误差separating funnel 分液漏斗 stopcock 玻璃活塞scissors 剪刀 spirit lamp 酒精灯silica gel G thin layer 硅胶G薄层板Ttable 片剂 tailing factor 拖尾因子tailing peak 拖尾峰 test solution 试液thermal analysis 热分析法 thermal conductivity detector 热导检测器thermogravimetric analysis 热重分析法The United States Pharmacopoeia 美国药典The Pharmacopoeia of Japan 日本药局方thin layer chromatography 薄层色谱thiochrome reaction 硫色素反应thymol 百里酚 thymolphthalein 百里酚酞实用标准文案titer 滴定度 three-dimensional chromatogram 三维色谱图titrant 滴定剂 titration error 滴定误差titrimetric analysis 滴定分析法 tolerance 容许限total ash 总灰分 total quality control 全面质量控制traditional drugs 传统药 traditional Chinese medicine 中药turbidance 浑浊 turbidimetric assay 浊度测定法turbidimetry 比浊度 turbidity 浊度Uultracentrifugation 超速离心 ultraviolet irradiation 紫外线照射undue toxicity 异常毒性 uniform design 均匀设计uniformity of dosage units 含量均匀度 uniformity of volume 装量均匀性uniformity of weight 重量均匀性Vvalidity 可靠性 variance 方差viscosity 粘度 volatile oil determination apparatus 挥发油测定器 volatilization 挥发性volumetric analysis 容量分析 volumetric solution 滴定液volumetric flasks 比重瓶Wwave length 波长 wave number 波数weighing bottle 称量瓶 weighing form 称量形式well-closed container 密闭容器 white board 白瓷板Xxylene cyanol blue FF 二甲苯蓝FF xylenol orange 二甲酚橙ZZigzag scanning 锯齿扫描 zwitterions 两性离子Zymolysis 酶解作用 zone electrophoresis 区带电泳文档大全。

药物分析常用英语词汇

药物分析常用英语词汇

药物分析专业英语词汇表Aabsorbance吸收度absorbanceratio吸收度比值absorption吸收absorptioncurve吸收曲线absorptioncoefficient吸收系数accuratevalue准确值Acid—dyecolormcty酸性染料比色法acidimcty酸量法acidity酸度activity活度adjustedretentiontime调整保留时间absorbent吸收剂absorption吸附alkalinity碱度alumina氧化铝,矾土ambienttemperature室温ammoniumthiocyanate硫氰酸铵analyticalqualitycontrol分析质量控制anhydroussubstance 干燥品antioxidant抗氧剂applicationofsample点样areanormalizationmethod面积归一法arsenic砷arsenicsport砷斑assay含量测定assaytolerance含量限度attenuation衰减acidburette酸式滴定管alkaliburette碱式滴定管amortar研钵Bbackextraction反萃取bandabsorption谱带吸收batch批batchnumber批号Benttendorlfmethod白田道夫法betweendayprecision日间密度精biotransformation生物转化blanktest空白试验boilingrange沸程BritishPharmacopeia英国药典bromatetitration溴酸盐滴定法brominemethod溴量法bromothymolblue溴麝香酚蓝bulkdrug原料药by—product副产物breaker烧杯buretteglassbeadnozzle滴定管brownacidburette棕色酸式滴定管Ccalibrationcurve校正曲线calomelelectrode甘汞电极calorimetry量热分析capacityfactor容量因子capillarygaschromatography毛细管气相色谱法carriergas载气characteristicsdescription性状chelatecompound螯合物chemicalequivalent化学当量Chinesepharmacopeia中国药典Chinesematerialmedicine中成药Chinesematerialmidicalpreparation中药制剂chiral手性的chiralcarbonatom手性碳原子chromatogram色谱图chromatography色谱法chromatographiccolumn色谱柱chromatographiccondition色谱条件clarity澄清度coefficientofdistribution分配系数coefficientofvariation变异系数colorchangeinterval变色范围colorreaction显色反应colormetry比色法columnefficiency柱效columntemperature柱温comparativetest比较试验completenessofsolution溶液的澄清度conjugate缀合物concentration—timecurve浓度时间曲线confidenceinterval置信区间confidencelevel置信水平controlledtrial对照试验correlationcoefficient相关系数contrasttest对照试验congealingpoint凝点contentunifarmity装量差异controlledtrial对照试验correlationcoefficient相关系数contrasttest对照试验counterion反离子cresalred甲酚红cuvettecell比色池cyanide氰化物casserolesmall勺皿Ddead—stoptitration永定滴定法deadtime死时间deflection偏差deflectionpoint拐点degassing脱气deionizedwater去离子水deliquescence潮解depressorsubstancestest降压物质检查法desiccant干燥剂detection检查developingreagent展开剂developingchamber展开室deviation偏差dextrose右旋糖diastereoisomer非对映异构体diazotization重氮化differentialthermalanalysis差示热分析法differentialscanningcalorimetry差示扫描热法Gutzeit古蔡daytodayprecision日间精密度dissolution溶出度directinjection直接进样2,6-dichlorindophenoltitration2,6-二氯靛酚滴定法digestion消化diphastictitration双向滴定disintegrationtest崩解试验dispersion分散度dissolubility溶解度dissolutiontest溶解度检查distillingrange滴程distributionchromatography分配色谱dose剂量drugqualitycontrol药品质量控制dryingtoconstantweight干燥至恒重duplicatetest重复试验diskmethodwatermethod压片法Eeffectiveconstituent有效成分effectiveplatenumber有效板数effectiveofcolumn柱效electrophoresis电泳elimination消除eluate洗脱液elution洗脱enamtiomer对映体endabsorption末端吸收endogenoussubstances内源性物质enzymedrug酶类药物enzymeinduction酶诱导enzymeinhibition酶抑制epimer差向异构体equilibriumconstant平衡常数errorinvolumetricanalysis容量分析误差exclusionchromatography排阻色谱法expirationdate失效期externalstandardmethod外标法extract提取物extrationgravimetry提取重量法extractiontitration提取容量法extrapolatedmethod外插法Erlenmeyerflask锥形瓶evaporatingdishsmall蒸发皿elongatedbulb胖肚electronicbalanceMettlerAL204MettlerAL204电子天平Ffactor系数fehling’sreaction斐林实验filter过滤finenessoftheparticles颗粒细度flowrate流速fluorescentagent荧光剂fluorescencespectrophotometry荧光分光光度法fluorescencedetection荧光检测器fluorescenceanalysis荧光分析法foreignpigment有色杂质formulary处方集free游离freezingtest冻结试验fusedsilica熔融石英filterpaper滤纸Ggaschromatography气相色谱法gas-liquidchromatography气液色谱法gaspurifier气体净化器Generalidentificationtest一般鉴别试验generalnotices凡例Generalrequirements(药典)通则goodclinicalpractices药品临床管理规范goodlaboratorypractices药品实验室管理规范goodmanufacturingpractices(GMP)药品生产质量管理规范goodsupplypractices(GSP)药品供应管理规范gradientelution梯度洗脱grating光栅gravimetricmethod重量法Gutzeittest古蔡(检砷)法glassfunnellongstem玻璃漏斗gradcylinder量筒glassrod玻棒graduatedpipettes刻度吸管GC气相色谱Hheavymetal重金属halfpeakwidth平峰宽heatconductivity热导率heightequivalenttoatheoreticalplate理论塔板高度heightofaneffectiveplate有效塔板高度high-performanceliquidchromatography(HPLC)高效液相色谱法high-performancethin-layerchromatography(HPTLC)高效薄层色谱法hydrate水合物hydrolysis水解hydrophilicity亲水性hydrophobicity疏水性hydroxylvalue羟值hyperchromiceffect浓色效应hypochromiceffect淡色效应HHS-typeconstanttemperaturewaterbathHHS型恒温水锅HPLC高效液相色谱法Iidentification鉴别ignitiontoconstantweight灼烧至恒重immobilephase固定相immunoassay免疫测定impurity杂质inactivation失活index索引indicatorelectrode指示电极indicator指示剂inhibitor抑制剂injectingseptum进样隔膜胶垫instrumentalanalysis仪器分析injectionvalue进样阀insulinassay胰岛素生物检测法integrator积分仪intercept截距interface接口internalstandardsubstance内标物质Internationalunit国际单位invitro体外invivo体内iodide碘化物iodoformreation碘仿反应iodometry碘量法ionpairchromatography离子对色谱ionsuppression离子抑制ionsuppression离子抑制ionicstrength离子强度ion-pairingagent离子对试剂ionization电离isoabsorptivepoint等吸收点isocraticelution等溶剂组成洗脱isoelectricpoint等电点isoosmoticsolution等渗溶液irreversibleindicator不可逆指示剂irreversiblepotential不可逆电位KKarlFischertitration卡尔-费舍尔滴定Kjeldahlmethodfornitrogen凯氏定氮法Koberreagent 科伯试剂Kovatsretentionindex科瓦茨保留指数Llabelledamount标示量leadingpeak前延峰levelingeffect均化效应licensedpharmacist执业药师limitcontrol限量控制limitofdetection检测限limitofquantitation定量限limittest杂质限度试验lossondrying干燥失重lowpressuregradientpump氧压梯度泵linearityandrange线性及范围linearityscanning线性扫描luminescence发光litmuspaper石蕊试纸lyophilization冷冻干燥Mmainconstituent主成分make-upgas尾吹气maltolreaction麦芽酚试验Marquistest马奎斯试验massanalyzerdetector质量分析检测器massspectrometricanalysis质谱分析massspectrum质谱图meandeviation平均偏差meltingpoint熔点meltingrange熔距metabolite代谢物metastableion亚稳离子micellarchromatography胶束色谱法microanalysis微量分析microcrystal微晶microdialysis微透析migrationtime迁移时间Milliporefiltration微孔过滤mobilephase流动相molecularformula分子式monitor检测monochromator单色器monographs正文Nnaturalproduct天然产物Nessler’sreagent碱性碘化汞试液neutralization中和nitrogencontent总氮量nonaqueousacid-basetitration非水酸碱滴定nonprescriptiondrug,overthecounterdrugs非处方药nonspecificimpurity一般杂质non-volatilematter不挥发物normalphase正相normalization归一化法Nesslercolorcomparisontube纳氏比色管Onotice凡例octadecylsilanebondedsilicagel十八烷基硅烷键合硅胶odorless辛基硅烷odorless无臭officialname法定名officialtest法定试验on-columndetector柱上检测器on-columninjection柱头进样onthedriedbasis按干燥品计opalescence乳浊opticalactivity光学活性opticalisomerism旋光异构opticalpurity光学纯度organicvolatileimpurities有机挥发性杂质orthogonaltest正交试验orthophenanthroline邻二氮菲outlier可疑数据overtones倍频封oxidation-reductiontitration氧化还原滴定oxygenflaskcombustion氧瓶燃烧Ppackedcolumn填充柱packingmaterial色谱柱填料palladiumioncolorimetry钯离子比色法parention母离子particulatematter不溶性微粒partitioncoefficient分配系数patternrecognition(ppm)百万分之几peaksymmetry峰不对称性peakvalley峰谷peakwidthathalfheight半峰宽percenttransmittance透光百分率pHindicatorabsorbanceratiomethodpH指示剂吸光度比值法pharmaceuticalanalysis药物分析pharmacopeia药典pharmacy药学photometer光度计polarimetry旋光测定法polarity极性polydextrangel葡聚糖凝胶potentiometer电位计potentiometrictitration电位滴定法precipitationform沉淀形式precision精密度preparation制剂prescriptiondrug处方药pretreatment预处理primarystandard基准物质principalcomponentanalysis主成分分析prototypedrug原型药物purification纯化purity纯度pyrogen热原pycnometermethod比重瓶法plasticwashbottle洗瓶platformbalance天平pipette移液管pyknowmeterflasks容量瓶Qqualitycontrol质量控制qualityevaluation质量评价qualitystandard质量标准quantitativedetermination定量测定quantitativeanalysis定量分析quasi-molecularion准分子离子Rracemization消旋化randomsampling随机抽样rationaluseofdrug合理用药readilycarbonizablesubstance易炭化物质reagentsprayer试剂喷雾剂recovery回收率referenceelectrode参比电极relatedsubstance相关物质relativedensity相对密度relativeintensity相对强度repeatability重复性replicatedetermination平行测定reproducibility重现性residualbasichydrolysismethod剩余碱水解法residualliquidjunctionpotential残余液接电位residualtitration剩余滴定residuceonignition炽灼残渣resolution分辨率responsetime响应时间retention保留reversedphasechromatography反相色谱法reverseosmosis反渗透rinse淋洗robustness可靠性round修约reagentbottles试剂瓶roundbottomflask圆底烧瓶rubbersuctionbulb洗耳球Ssafety安全性Sakaguchitest坂口试验saltbridge盐桥saltingout盐析sampleapplicator点样器sampleapplication点样sampling取样saponificationvalue皂化值saturatedcalomelelectrode饱和甘汞电极selectivity选择性significantdifference显着性水平significanttesting显着性检验silicaget硅胶silverchlorideelectrode氯化银电极similarity相似性sodiumdodecylsulfate十二基酸钠solid-phaseextraction固相萃取solubility溶解度specificabsorbance吸收系数specification规格specificity专属性specificrotation比旋度specificweight比重spiked加入标准的splitinjection分流进样sprayreagent显色剂stability稳定性standardcolorsolution标准比色液standarddeviation标准差standardization标定standardsubstance标准品statisticalerror统计误差sterilitytest无菌试验stocksolution储备液stoichiometricpoint化学计量点storage贮藏straylight杂散光substrate底物substituent取代基sulfate硫酸盐sulphatedash硫酸盐灰分support载体suspension旋浊度swellingdegree膨胀度symmetryfactor对称因子systematicerror系统误差separatingfunnel分液漏斗stopcock玻璃活塞scissors剪刀spiritlamp酒精灯silicagelGthinlayer硅胶G薄层板Ttable片剂tailingfactor拖尾因子tailingpeak拖尾峰testsolution试液thermalanalysis热分析法thermalconductivitydetector热导检测器thermogravimetricanalysis热重分析法TheUnitedStatesPharmacopoeia美国药典ThePharmacopoeiaofJapan日本药局方thinlayerchromatography薄层色谱thiochromereaction硫色素反应thymol百里酚thymolphthalein百里酚酞titer滴定度three-dimensionalchromatogram三维色谱图titrant滴定剂titrationerror滴定误差titrimetricanalysis滴定分析法tolerance容许限totalash总灰分totalqualitycontrol全面质量控制traditionaldrugs传统药traditionalChinesemedicine中药turbidance浑浊turbidimetricassay浊度测定法turbidimetry比浊度turbidity浊度Uultracentrifugation超速离心ultravioletirradiation紫外线照射unduetoxicity异常毒性uniformdesign均匀设计uniformityofdosageunits含量均匀度uniformityofvolume装量均匀性uniformityofweight重量均匀性Vvalidity可靠性variance方差viscosity粘度volatileoildeterminationapparatus挥发油测定器volatilization挥发性volumetricanalysis容量分析volumetricsolution滴定液volumetricflasks比重瓶Wwavelength波长wavenumber波数weighingbottle称量瓶weighingform称量形式well-closedcontainer密闭容器whiteboard白瓷板XxylenecyanolblueFF二甲苯蓝FFxylenolorange二甲酚橙ZZigzagscanning锯齿扫描zwitterions两性离子Zymolysis酶解作用zoneelectrophoresis区带电泳。

两种现象做比较的英语作文题目

两种现象做比较的英语作文题目

两种现象做比较的英语作文题目Comparison of Two PhenomenaThe world we live in is a complex and multifaceted place, filled with a myriad of phenomena that captivate our attention and challenge our understanding. In this essay, we will explore and compare two distinct phenomena that have significant impacts on our lives and the broader societal landscape.The first phenomenon we will examine is the rapid advancements in technology and its transformative effects on our daily routines and the way we interact with the world around us. Over the past few decades, we have witnessed an unprecedented surge in technological innovations, from the ubiquitous smartphones that have become extensions of our very beings to the revolutionary breakthroughs in artificial intelligence and automation that are reshaping entire industries. The integration of technology into almost every aspect of our lives has brought about both remarkable conveniences and profound societal shifts.On one hand, the technological revolution has empowered us with unprecedented access to information, communication, andentertainment. With a few taps on our screens, we can instantly connect with loved ones across the globe, access a wealth of knowledge at our fingertips, and immerse ourselves in captivating digital experiences. This has led to a more interconnected world, where geographical boundaries have become increasingly blurred, and the exchange of ideas and cultural experiences has been greatly facilitated.Moreover, the advancements in technology have also transformed the way we work and conduct business. The rise of remote work, cloud-based collaboration, and intelligent automation has enabled greater flexibility, efficiency, and productivity in the workplace. Employees can now work from the comfort of their homes, collaborate seamlessly with teams dispersed across the world, and delegate mundane tasks to intelligent algorithms, freeing up time and resources for more strategic and creative endeavors.However, the ubiquity of technology has also brought about significant challenges and concerns. The constant bombardment of digital stimuli has led to increased levels of distraction, anxiety, and social isolation, as individuals struggle to maintain a healthy balance between their online and offline lives. The reliance on technology has also raised privacy and security concerns, as personal data and sensitive information become increasingly vulnerable to cyber threats and misuse.Furthermore, the rapid pace of technological change has disrupted traditional industries and business models, leading to job displacement and the need for workers to continuously upskill and adapt to new demands. The fear of automation and artificial intelligence replacing human labor has become a source of anxiety for many, as the long-term societal implications of these technological advancements remain uncertain.The second phenomenon we will examine is the growing awareness and concern for environmental sustainability and the urgent need to address the pressing challenges posed by climate change. In recent years, the global community has witnessed a surge in environmental activism, with individuals and organizations alike recognizing the grave consequences of human-induced environmental degradation and the imperative to adopt more sustainable practices.The effects of climate change, such as rising sea levels, extreme weather events, and the depletion of natural resources, have become increasingly evident and pose a significant threat to the well-being of our planet and its inhabitants. This has led to a heightened sense of responsibility and a call for collective action to mitigate the impact of our actions on the environment.One of the most notable manifestations of this environmentalconsciousness is the rise of renewable energy sources, such as solar, wind, and hydropower, as viable alternatives to fossil fuels. Governments, businesses, and individuals are increasingly investing in and adopting these clean energy solutions, driven by a desire to reduce carbon emissions and contribute to a more sustainable future.Additionally, there has been a growing emphasis on sustainable consumption and production practices, with consumers becoming more mindful of their purchasing decisions and the environmental impact of the goods and services they consume. This has led to the proliferation of eco-friendly products, the implementation of circular economy models, and the promotion of sustainable lifestyle choices, such as reducing waste, recycling, and adopting plant-based diets.However, the transition towards environmental sustainability is not without its challenges. The shift away from established industries and practices often faces resistance from vested interests and requires significant financial investments and political will to overcome. Furthermore, the uneven distribution of the impacts of climate change, with developing countries often bearing the brunt of the consequences, has raised questions of global equity and the need for collaborative international efforts to address these complex issues.In conclusion, the comparison of these two phenomena – the technological revolution and the growing environmentalconsciousness – reveals the multifaceted and interconnected nature of the challenges and opportunities we face as a global society. While the advancements in technology have brought about remarkable conveniences and transformative changes, they have also given rise to new concerns and societal disruptions. Similarly, the heightened awareness of environmental sustainability has catalyzed positive changes, but the path towards a truly sustainable future remains fraught with obstacles.As we navigate these complex landscapes, it is crucial that we strive to strike a delicate balance between technological progress and environmental stewardship, leveraging the power of innovation to address the pressing environmental challenges we face. By fostering collaborative efforts, embracing sustainable practices, and cultivating a deeper understanding of the intricate relationships between technology and the natural world, we can work towards a future that is both technologically advanced and environmentally responsible, ensuring the well-being of our planet and the generations to come.。

PHt伤口愈合

PHt伤口愈合

Up-Regulation of Keratinocyte Growth Factor and Receptor:A Possible Mechanism of Action of Phenytoin in Wound HealingSwarga Jyoti Das and Irwin Olsen 1Department of Periodontology,Eastman Dental Institute for Oral Health Care Sciences,University College London,University of London,256Gray’s Inn Road,London WC1X 8LD,United KingdomReceived March 7,2001A number of studies suggest that keratinocyte growth factor (KGF)plays a major part in reepitheli-alisation after injury,via binding to the specific KGF receptor (KGFR).Several pharmacological agents,in-cluding the anti-epileptic drug phenytoin (PHT),have been widely used clinically to promote wound healing.Although the mechanism of action of PHT in this pro-cess is still not well understood,it is possible that the activity of PHT in wound healing is mediated via KGF and the KGFR.In the present study,using the enzyme-linked immunosorbant assay and flow cytometry we have shown that PHT increases KGF secretion and KGFR expression by more than 150%in gingival fibro-blasts and epithelial cells,respectively.Moreover,semi-quantitative reverse transcriptase-polymerase chain reaction analysis showed that PHT also mark-edly increased both KGF and KGFR gene transcrip-tion by these cells.Our findings thus suggest that the wound healing activity of PHT in vivo may be medi-ated,at least partly,via KGF and its receptor.©2001Academic PressKey Words:ELISA;FGF;flow cytometry;KGF;KGFR;phenytoin;regeneration;RT-PCR;wound healing.Wound healing is a complex process involving cell migration,proliferation,differentiation,and the for-mation of new extracellular matrix (1).Many of these events are controlled by growth factors and are medi-ated by the transduction of intracellular signals follow-ing the binding of the factors to specific transmem-brane tyrosine kinase receptors.The role of growth factors specific for epithelial cells is,for example,ofmajor importance in the regrowth of damaged epithe-lial tissues,which occurs rapidly after injury (2,3).Keratinocyte growth factor (KGF)is the seventh member of the fibroblast growth factor (FGF)family and has 30to 45%homology with the other members of the FGF family.It is synthesised and secreted by mes-enchymal cells such as fibroblasts and is a potent mi-togen for a wide variety of epithelial cells (4).KGF acts via the KGF receptor (KGFR),which is a splice variant of the FGF receptor-2/bek gene that binds both KGF and acidic FGF with high affinity and basic FGF with lower affinity (5).However,KGFR is expressed only by epithelial cells,whereas FGF receptor-2is expressed by several different cell types (6).There is substantial evidence that KGF is involved in the wound healing process since KGF transcripts have been reported to be markedly up-regulated within 24h of injury (7)and an enhanced rate of epithelial regeneration has been observed following topical appli-cation of recombinant KGF (8,9).In addition,a rela-tively lower level of this growth factor has been ob-served in wound tissues in certain conditions associated with impaired wound healing (10,11).Se-vere delay in wound reepithelialisation in transgenic KGFR-knockout mice also suggests the importance of KGFR signalling in wound healing processes (12).Wound healing has also been shown to be en-hanced by a number of pharmacological agents,in-cluding phenytoin (PHT),a potent anti-epileptic drug.Accelerated repair of periodontal wounds with reduced postsurgical inflammation and pain was first noted with PHT in 1958(13)and,subsequently,in the healing of dental extraction sockets (14).Favourable results have also been reported with top-ical application of PHT in the treatment of various types of ulcers,burns,abscess cavities,and surgical wounds (15,16).In addition,PHT has been used to treat lichen planus and discoid lupus erythematosus,although with variable success (17).1To whom correspondence and reprint requests should be ad-dressed.Department of Periodontology,Room RL 16Levy Wing,Eastman Dental Institute for Oral Health Care Sciences,University College London,University of London,256Gray’s Inn Road,London WC1X 8LD,UK.Fax:0044(0)207915-1254.E-mail:iolsen@.Biochemical and Biophysical Research Communications 282,875–881(2001)doi:10.1006/bbrc.2001.4621,available online at onDespite numerous clinical trials and case studies, however,the mechanism of action of PHT in wound healing is still not well understood.Since KGF and KGFR have been shown to play a pivotal part in tissue repair processes,it is possible that the action of PHT is mediated at least partly via this growth factor and its receptor.In the present study we have therefore exam-ined the effects of PHT on the expression of KGF and KGFR and on the activity of their corresponding genes in gingival cells in vitro,as a model of the wound healing effects of PHT in vivo.MATERIALS AND METHODSPreparation of PHT.PHT(Sigma,Poole,UK)was dissolved in 100%ethanol(BDH,Laboratory supplies,Poole,UK)to obtain a stock solution of5mg/ml.It was used atfixed concentration of5and 10␮g/ml in the experiments described below.The samefinal con-centration of ethanol was used in both the control and PHT-containing media.Cell culture.Normal gingival tissue samples were obtained un-der the Eastman Dental Institute and Hospital Joint Ethics and Research Committee.Confluent cultures of gingivalfibroblast(GF) cells were obtained by incubating biopsy samples of normal gingiva (NG)fromfive healthy individuals(three males and two females;age range30to40years,mean age35Ϯ7.1),as previously described (18).The cells were detached from the monolayer by treating them with0.25%trypsin in1mM ethylenediaminetetraacetic acid(EDTA) (Gibco Life Technologies Ltd.,Paisley,UK),collected by centrifuga-tion and serially passaged in25cm2tissue cultureflasks(Falcon, Becton Dickinson Labware;Cowley,UK).The number and viability of the cells were determined by trypan blue staining at the time of each passage.Cells at the3rd–5th passages were used in this study. Gingival epithelial cells(GE)were grown from the epithelium, which was separated mechanically from the connective tissue of the excised normal gingiva.The epithelial tissue was cut into1mm3 pieces and cultured at37°C in a humidified atmosphere of air with 5%CO2in Keratinocyte Basal Medium-2(KBM-2)containing whole bovine pituitary extract,recombinant human epidermal growth fac-tor(rh EGF),insulin,hydrocortisone,transferrin,epinephrine,and gentamycin(BioWhittaker;Wokingham,UK).When individual col-onies of the outgrowth of the GE cells reached an average size of between50to200cells,they were detached using trypsin-EDTA and serially passaged.The viability of the GE cells was confirmed by trypan blue exclusion at the time of passage.The purity of the GE cell culture was ascertained by positive staining of the cells with an antibody(clone MNF116)against cytokeratins5,6,8,and17(Dako Ltd.,High Wycombe,UK)(data not shown).Cells at the2nd and3rd passages were used in this study.Treatment offibroblasts with PHT:KGF secretion.GF cells were seeded at a density of2ϫ104into24-well tissue culture plates (Falcon)and incubated until they become confluent.The medium was then replaced with fresh medium containing1%FCS for48h, after which the medium was replaced with fresh1%FCS-containing medium in the absence and presence of5and10␮g/ml of PHT.These concentrations were selected on the basis of posttherapeutic serum levels(19).A sample of the supernatant was removed from each of three replicate wells on each of4subsequent days of incubation, centrifuged at13,000rpm for1min and stored atϪ20°C.The amount of KGF secreted by the cells into the culture medium was measured by ELISA,as described previously(20).Briefly,96-well microtitre plates(Immulon4)(Dynex Technologies,Inc.,Chan-tilly,VA)were coated with5␮g/ml of a mouse monoclonal antibody (mAb)against human KGF(preparation number IG4)(Amgen Inc., Thousand Oaks,CA)in carbonate-bicarbonate buffer(pH9.6)and incubated at4°C overnight.The wells were washed three times with phosphate buffer saline(PBS)containing0.1%Tween20(PBS-T) (BDH)and nonspecific protein binding sites were blocked using200␮l of PBS containing1%(w/v)bovine serum albumin(BSA)(BDH) for1h at room temperature.After washing,100␮l of the culturesupernatants to be tested were added to three replicate wells and incubated for2h at room temperature.The washing step was re-peated and biotinylated mAb against human KGF(preparation num-ber A1)(Amgen),diluted to20ng/ml in PBS containing0.2%BSA and0.02%Tween20,was added for30min at room temperature. The plates were washed again and the binding of the biotinylated mAb was detected by incubation with a1:1000dilution of extravidin-peroxidase(Sigma),for30min at room temperature,followed by incubation with100␮l of3,3Ј,5,5Ј-tetramethyl-benzidine(ICN Bio-medicals,Costa Mesa,CA)in0.1M citrate-phosphate buffer(pH5.0) containing0.03%hydrogen peroxide(Sigma)for30min at37°C.The reaction was terminated by the addition of50␮l of2M H2SO4and the absorbance at450nm measured spectrophotometrically(Titer-tek Multiskan Plus,Helsinki,Finland).The concentration of KGF in the supernatant was calculated from a standard curve constructed by using between0.31and5.00ng/ml of recombinant human KGF (Amgen)in complete medium containing1%FCS.The results shown are derived from the average of three replicate wells for each time point in each experiment.Flow cytometry(FCM)analysis of KGFR expression by GE cells. GE cells were grown in25cm2tissue cultureflasks to80%confluency in KBM-2and then for48h in the absence of rh EGF.The medium was then replaced by fresh medium without EGF incubated in the absence and presence of10␮g/ml of PHT for3days and the cells prepared for FCM as described previously(21).Briefly,the cells were detached using20mM EDTA in PBS,centrifuged andfixed with3% paraformaldehyde.Aliquots of105cells were stained with an affinity-purified rabbit polyclonal antibody against human KGFR/ FGFR-2(C-17)(Santa Cruz Biotechnology,CA)for1h at room temperature and washed with PBS containing saponin,to permea-bilise the cells,and sodium azide(wash buffer).They were then incubated withfluorescein isothiocyanate(FITC)-labelled swine anti-rabbit antibody(Dako).Cells incubated with only secondary antibody were used as negative control.The averagefluorescence intensity(AFI)was measured using a FACScanflow cytometer(Bec-ton Dickinson,Oxford,UK).The experiments were carried out twice using each of thefive cell lines.Extraction of RNA and RT-PCR analysis of KGF and KGFR.The GF and GE cells were incubated in the absence and presence of PHT for3days,as described above.The cells were harvested using trypsin-EDTA and total RNA isolated as described previously(22). The RNA was measured by absorbance at260nm using an Ultrospec 2000spectrophotometer(Pharmacia Biotech,Cambridge,UK).Pro-tein contamination of the RNA preparations was assessed by mea-suring the absorbance at280nm.Thefirst strand of cDNA was synthesized from the total RNA using an oligonucleotide(oligo dT)primer(Promega,Madison,WI) and cloned Moloney murine leukaemia virus reverse transcriptase (Stratagene,Cambridge,UK).The resulting cDNA prepared from RNA extracted from the GF and GE cells were amplified using primer pairs specific for the KGF and KGFR genes,respectively.The primer pair used to amplifying KGF cDNA had the sequences[tct gtc gaa cac agt ggt acc t]and[gtg tgt cca ttt agt tga tgc at]for the forward and reverse direction,respectively,generating an expected PCR product of266bp(23).The primer pair used for amplification of KGFR cDNA was[tcg ggg ata aat agt ttc caa tg]and[ctg ttt tgg cag gac agt ga]for the forward and reverse direction,respectively,and generates a PCR product of141bp(6).In addition,the housekeeping gene glyceraldehyde-3-phosphate dehydrogenase(GAPDH)was am-plified at the same time and under the same PCR conditions as those for KGF and KGFR.The expression of the GAPDH gene is consid-ered to be constitutive and was used in this study as an internal standard for estimating the relative level of KGF and KGFR mRNA.The primer sequences used for amplification of the GAPDH cDNA,as used in previous study,was [cca ccc atg gca tcc cat ggc a]and [ctg gac ggc agg tca ggt cca cc]for the forward and reverse direction,respec-tively,generating a product of 600bp (23).All three pairs of primers used in this study were obtained from Amersham Pharmacia Biotech (Amersham,UK).All PCR reactions were carried out within a linear range (25and 30cycles for KGF and KGFR,respectively),as initially determined by PCR amplification in 5-cycle steps,from 15to 40cycles (data not shown).The amplification programme consisted of initial denatur-ation at 96°C for 3min,followed by repeated cycles of denaturation at 95°C for 30s,annealing at 60°C for 30s,extension at 72°C for 90s,and final extension at 72°C for 10min.The amplified PCR products were identified by comparing the electrophoretic mobility of the predicted product with that of a 100bp DNA size marker (Helena Biosciences Ltd.,Sunderland,UK).The PCR reaction was repeated twice for each sample with different RNA from each separate tissue culture experiment.To determine the relative amount of KGF mRNA transcripts present in each sample,the intensities of the KGF and GAPDH PCR bands in the same lane of each gel were measured using the Scion Image Software Programme (Scion Corporation,Frederick,MD).The intensity of the amplified GAPDH product was taken as the baseline value and the ratio of the KGF band to the GAPDH band intensity in each sample was calculated.These ratios were used as a measure of the relative expression of KGF mRNA in each of the samples,which is shown as a KGF expression index (KFI):KFI ϭintensity of KGF band/intensity of GAPDH band ϫ100.Further,the KFI of each PHT-treated cell sample was compared with the KFI of the control cells and expressed as the KFI relative to the control.The relative amount of KGFR transcripts in each sample was measured in a similar way as that of the KGF transcripts and calculated as the KGFR expression index (KRI).The KRI of each PHT-treated cell sample was compared with the KRI of the control cells and expressed as the KRI relative to the control.DNA sequencing.The amplified PCR products were purified from the agarose gels by using the QIAquick gel extraction kit (QIAGEN Ltd.,West Sussex,UK)and amplified using the forward primer of each of the primer pairs used to amplify KGF and KGFR cDNA and the DNA sequencing kit (Applied Biosystem,Warrington,UK).The amplified product was then analysed by capillary electrophoresis using the automatic ABI PRISM DNA sequencing analysis software (310Genetic analyzer)(Perkin Elmer,Cambridge,UK).The nucle-otide sequence obtained was compared with the sequence submittedoriginally for the KGF (Accession No.M25295)(24)and KGFR gene (Accession No.M80634)(6).Statistical analysis.The data were analysed by using a paired two-tailed Student’s t test.Values of P Յ0.05were considered as statistically significant.RESULTSCellular reaction to PHT.The characteristic elon-gated,spindle-shaped morphology of GF cells was maintained even after incubation for 7days in the presence of 5and 10␮g/ml of PHT.In addition,when the cells were stained with trypan blue to evaluate their viability,no deleterious effect of the drug was detectable (data not shown).PHT was also observed to be similarly nontoxic and to have no apparently detri-mental effect on the GE cells.Effect of PHT on KGF secretion.ELISA assay of the culture media of the control and PHT-treated GF cells was carried out to determine the effects of PHT on KGF secretion during 4days of culture,as shown in Fig.1.Relatively low levels of KGF were present in the su-pernatants of the control cultures (average of 1.18Ϯ0.09ng/ml;range 0.78to 1.47ng/ml).In marked con-trast,much greater amounts of KGF were secreted into the culture media of cells incubated with PHT,reach-ing maximum levels on day 3with both drug concen-trations (1.95Ϯ0.33ng/ml;range 1.48to 1.99ng/ml and 2.66Ϯ0.39ng/ml;range 1.97to 2.66ng/ml,with 5␮g/ml and 10␮g/ml of PHT,respectively).A greater amount of KGF secretion was observed at all time periods at the concentration of 10␮g/ml compared with 5␮g/ml of PHT.The amount of KGF secretion induced by PHT,rel-ative to the control cultures,is shown in Table 1.The maximum relative levels of KGF secretion were on day 1,and were 1.9and 2.5times greater than the control level with 5and 10␮g/ml of PHT,respectively.Effect of PHT on KGF gene transcription.In order to determine whether the elevated levels of KGF secre-TABLE 1Effects of PHT on KGF Secretion by GF Cells in VitroIncubation time(days)Relative level of KGF secretionPHT (5␮g/ml)PHT (10␮g/ml)1 1.9(0.33–2.49) 2.5*(0.41–3.31)2 1.8(0.44–3.28) 2.3(1.09–3.49)3 1.3(0.86–2.91) 1.8(1.21–4.35)41.4(0.45–3.08)1.8(0.79–4.90)Note.The values shown are the relative average amounts of KGF secretion ϮSEM in the PHT-treated cultures compared with the control cultures,defined as 1.0.The range of secretion levels is shown in brackets,and the maximum relative secretion in the PHT-treated cultures is shown in bold type.*Statistically significant difference compared with controls (P Ͻ0.05).FIG.1.Effects of PHT on KGF secretion by GF cells.Cultures of normal gingival fibroblasts were incubated in the absence (white bars)and presence of 5␮g/ml (black bars)and 10␮g/ml (grey bars)of PHT.The data shown is the average of triplicate assays from ten separate experiments ϮSEM (vertical lines).tion induced by PHT in vitro was associated with in-creased transcription of the respective gene,semi-quantitative PCR was carried out using GAPDH as the internal control,as described under Materials and Methods.Figure 2shows a representative gel and the corresponding image analysis profiles of the RT-PCR products of GF cells cultured in the absence and pres-ence of PHT.All the samples showed the single band corresponding to the predicted molecular size of the GAPDH gene sequence (600bp),confirming that the RNA extracted from the samples was intact and not degraded.In addition to this GAPDH band,the band corresponding to the KGF gene sequence (266bp)was observed in the control as well as the PHT-treated cells.The surface areas of the histograms obtained from image analysis of the GAPDH and KGF band intensities were considered to be equivalent to the lev-els of the respective mRNAs in the samples.The rela-tive expression of KGF gene transcripts,defined as the KFI,was calculated from these histogram profiles.The KFI values obtained in this representative experiment were 19for the control cells and 28and 47for the cells treated with 5and 10␮g/ml of PHT,respectively (1.5and 2.4times the control level,respectively).The overall average KFI for the five control cell line in duplicate experiments was found to be 17Ϯ3(range 6to 34),whereas cells incubated with 5and 10␮g/ml of PHT produced KFI values of 26Ϯ6(range 11to 58)and 34Ϯ8(range 14to 75),respectively.Thus,incu-bation of GF cells in the presence of 5and 10␮g/ml of PHT up-regulated the activity of the KGF gene by approximately 150and 200%,respectively,and these differences were statistically significant (P Ͻ0.05).Effect of PHT on KGFR expression.To examine the effect of PHT on KGFR expression,the GE cells were immunostained with antibody specific for FGFreceptor-2and analysed by FCM,as described under Materials and Methods.Representative fluorescence pro-files of KGFR expression are shown in Fig.3and dem-onstrate that the relative level of this antigen in the PHT-treated cells was 180%higher than in the control cells (AFI values of 202and 115,respectively).In ten experiments using five cell lines in duplicate,the average relative level of KGFR expression in the PHT-treated cells was calculated to be 161Ϯ22(range 66to 200)using 10␮g/ml of PHT,which was 1.5times the control level (AFI of 100Ϯ15;range 49to 139).This difference was found to be statistically significant (P Ͻ0.05).Effect of PHT on KGFR gene transcription.A rep-resentative PCR gel of KGFR and the image analysis profiles are shown in Fig. 4.Integrity of the RNA samples was shown by the presence of the single band of the GAPDH gene sequence (600bp).A band corre-sponding to the KGFR gene sequence (141bp)was also observed in both the control and PHT-treated cells.The image analysis profiles of the relative intensities of the GAPDH and KGFR bands,expressed as the KRI,indicated that the KRI value in the PHT-treated cells was higher than in the control cells (64and 43,respectively).The overall KRI of ten experiments using five cell lines in duplicate was found to be 42Ϯ6(range 19to 70)with 10␮g/ml of PHT,whereas it was 28Ϯ4(range 16to 43)in the control cells.Thus,incubation of the GE cells in the presence of PHT up-regulated the activity of the KGFR gene by approximately 150%,although this difference was not statistically significant (P Ͼ0.05).Specificity of PCR products.The nucleotide se-quences obtained from the DNA sequencing PCR of KGF and KGFR were identical to the previously re-ported sequences for KGF (22)and KGFR (6),thusFIG.2.Effects of PHT on KGF gene transcription in GF cells.A representative experiment showing the RT-PCR analysis of the GF cells cultured in the absence and presence of 5and 10␮g/ml of PHT for 3days.Each panel shows the electrophoretic mobility of the RT-PCR products and the corresponding image analysis of these bands:A,control cultures;B and C,GF cells incubated with 5and 10␮g/ml of PHT,respectively.Note the presence of GAPDH bands (600bp)of similar intensity in all three panels and increasing amounts of the KGF gene product (266bp)in panels B and C.Numbers in brackets are the KFI values in this experiment,which are 19,21,and 47for the control,5and 10␮g/ml of PHT,respectively.confirming the specificity of the PCR products and also the primer pairs used to amplify the KGF and KGFR mRNA in this study (data not shown).DISCUSSIONWound healing is a complex series of cellular and molecular events which include inflammation,cell mi-gration,angiogenesis,matrix remodelling,and reepi-thelialisation.These entail the coordinated functions of many types of cell,including keratinocytes,fibroblasts,endothelial,and inflammatory cells,and are closely regulated by growth factors and cytokines.Reepitheli-alisation,involving keratinocyte migration and prolif-eration,is considered to be one of the major features of wound healing.KGF has been shown to enhance the migration and proliferation of keratinocytes (4,25)and is also involved in matrix remodelling (26).It is notable that KGF is involved not only in reepithelialisation during wound healing,but also in destruction of reac-tive oxygen species in keratinocytes by induction of glutathione peroxidase,thereby protecting the epider-mis from oxidative injury due to free radicals (27).The cellular events that occur during wound healing are also modulated by various pharmacological agents,including PHT.PHT is a widely used anti-epileptic drug,although it has a wide range of pharmacologic effects in addition to its anti-epileptic activity.Its pri-mary site of action appears to be within the motor cortex,where the spread of seizure activity is inhibited by a membrane potential-dependent blockade of Na ϩchannels and perhaps presynaptic Ca ϩchannels (28).However,PHT was also found to have a secondary therapeutic role in promoting the wound healing which accompanies the occurrence of gingival hyperplasia that affects approximately 50%of patients taking this drug (29).Subsequently,a number of clinical trials have provided evidence of an increased rate of repair with reduced oedema and inflammation and enhanced formation of granulation tissue following the topical application of PHT to cutaneous wounds (13,14,16,17).Since KGF and KGFR signalling events havebeenFIG.3.Effects of PHT on KGFR expression by GE cells.A repre-sentative experiment showing FCM analysis of the fluorescence profiles of 10,000cells derived from a control and 10␮g/ml of PHT-treated cultures.A solid vertical line is drawn arbitrarily on the histograms to indicate the mean AFI value of the KGFR positive cells in the control culture (115).Note that the profile of PHT-treated cells has shifted to right side of the vertical line,indicating a higher level of KGFR expres-sion in PHT-treated cells (AFI of 202).The dashed lines represent the profiles of the negative control cells in correspondingexperiment.FIG.4.Effects of PHT on KGFR mRNA transcripts in GE cells.Representative experiments of normal GE cells cultured in the absence and presence of PHT.Each panel shows the electrophoretic mobility of the RT-PCR products and the corresponding image analysis of these bands:A,control cultures;B,PHT-treated cultures.Note the presence of GAPDH bands (600bp)of similar intensity in both panels.The KRI values obtained from this representative experiment are 43and 64for the control and PHT-treated cells,respectively.strongly implicated in the remodelling of damaged ep-ithelial tissue in vivo(7–9),in the present study we have examined whether PHT up-regulates this growth factor and its receptor in vitro.Ourfindings demonstrate,for thefirst time,that PHT significantly increases KGF secretion and KGF gene transcription by GF cells.The reason for the wide variation which we found in KGF response is unclear, but may be related to the differential uptake,metabo-lism and binding of PHT to gingival cells obtained from different individuals(15).Although the precise effects of PHT on these cells has yet to be delineated,the up-regulation of KGF by PHT may be mediated via other growth factors,inflammatory mediators,hor-mones,and hormone antagonists which have been shown to regulate KGF expression in vitro and during wound healing in vivo(11,30–35).It is notable that recent studies have identified an-other member of the FGF family having a high degree of structural homology with KGF.However,unlike the original KGF studied here(KGF-1),this new growth factor,KGF-2,is mitogenic forfibroblasts as well as epithelial cells and has been shown to be involved in wound healing processes in vivo(36).Since the PCR primers and antibodies used in this study are specific for KGF-1,further studies are required to determine whether KGF-2is also modulated by PHT.KGFR has also been implicated in wound reepithe-lialisation,by signal transduction following the bind-ing of KGF(6).In addition,severe delay in the wound healing process has been reported in transgenic KGFR knockout mice(12).In the present study we used FCM to determine whether PHT also affected the expression of the KGFR.Although this technique measures rela-tive antigen levels,it is nevertheless proportional to the actual number of antigen molecules present in or on the cells(37).Moreover,the polyclonal antibody used for immunostaining of the GE cells was directed against the intracellular domain of the FGF receptor-2 which is present in the KGFR splice variant expressed by epithelial cells only(6).Furthermore,the GE cells were confirmed to be of epithelial lineage by positive staining for cytokeratins,as noted under Materials and Methods.However,their characteristic slow growth and short life span in primary culture limited the use of more than one concentration of PHT for measuring the KGFR response,in contrast to the KGF response by the more rapidly-growing and longer-lived GF cells. Ourfindings have demonstrated that relatively higher KGFR levels are expressed by the PHT-treated cells compared with the control GE cells,thereby providing increased KGFR availability to form biologically active complexes with KGF which could enhance reepitheli-alisation of PHT-treated wounds in vivo.As with KGF, however,while the precise mechanisms involved in the regulation of KGFR have yet to be identified,the ex-pression of this receptor is clearly subject to the influ-ence of growth factors and inflammatory cytokines which are expressed during the wound healing process (38).In conclusion,our study has shown that PHT in-duces both KGF and the KGFR at the protein level and also up-regulates the activity of the corresponding genes in vitro,suggesting the possibility that the action of PHT in wound healing in vivo may also be mediated at least partly via KGF and the KGFR. ACKNOWLEDGMENTSThe authors are grateful to the staff of the Periodontology Clinic, Eastman Dental Hospital,London,for generously providing redun-dant surgical materials.We also thank Amgen,Inc.(Thousand Oaks, CA)for providing the recombinant human KGF and mAbs against human KGF to carry out these experiments.S.J.Das acknowledges The Association of Commonwealth Universities for a Commonwealth Scholarship.REFERENCES1.Clark,R. A. F.(1993)Basics of cutaneous wound repair.J.Dermatol.Surg.Oncol.19,693–706.2.Risau,W.(1990)Angiogenic growth factors.Prog.Growth FactorRes.2,71–79.3.Pierce,G.F.,and Mustoe,T.A.(1995)Pharmacological enhance-ment of wound healing.Annu.Rev.Med.46,467–481.4.Rubin,J.S.,Osada,H.,Finch,P.W.,Taylor,W.G.,Rudikoff,S.,and Aaronson,S.A.(1989)Purification and characterisation of a newly identified growth factor specific for epithelial cells.Proc.A86,802–806.5.Ornitz,D.M.,Xu,J.,Colvin,J.S.,McEwan,D.G.,MacArthur,C.A.,Coulier,F.,Gao,G.,and Goldfarb,M.(1996)Receptorspecificity of thefibroblast growth factor family.J.Biol.Chem.271,15292–15297.6.Miki,T.,Bottaro,D.P.,Fleming,T.P.,Smith,C.L.,Burgess,W.H.,Chan,AM-L.,and Aaronson,S.A.(1991)Determination of ligand-binding specificity by alternative splicing:Two distinct growth factor receptors encoded by a single gene.Proc.Natl.A89,246–250.7.Werner,S.,Peters,K.G.,Longaker,M.T.,Fuller-Pace, F.,Banda,M.J.,and Williams,L.T.(1992)Large induction of keratinocyte growth factor expression in the dermis during wound A89,6896–6900.8.Pierce,G.F.,Yanagihara,D.,Klopchin,K.,Danilenko,D.M.,Hsu,E.,Kennery,W.C.,and Morris,C.F.(1994)Stimulation of all epithelial elements during skin regeneration by keratinocyte growth factor.J.Exp.Med.179,831–840.9.Staiano-Coico,L.,Krueger,G.J.,Rubin,J.S.,D’limi,D.,Vallat,L.,Valentino,L.,Fahey,T.,III,Hawes,A.,Kingston,G.,and Madden,M.R.(1993)Human keratinocyte growth factor effects in a porcine model of epidermal wound healing.J.Exp.Med.178, 865–878.10.Werner,S.,Breeden,M.,Hubner,G.,Greenhalgh,D.G.,andLongaker,M.T.(1994)Induction of keratinocyte growth factor expression is reduced and delayed during wound healing in the genetically diabetic mouse.J.Invest.Dermatol.103,469–473.11.Brauchle,M.,Fassler,R.,and Werner,S.(1995)Suppression ofkeratinocyte growth factor expression by glucocorticoids in vitro and during wound healing.J.Invest.Dermatol.105,579–584.12.Werner,S.,Smola,H.,Liao,X.,Longaker,M.T.,Kreig,T.,Hofschneider,P.H.,and Williams,L.T.(1994)The function of。

关于对比的英文花式表达

关于对比的英文花式表达

关于对比的英文花式表达Literary Devices for Contrasting Ideas: A Comprehensive Guide.In the realm of written expression, the ability to effectively convey contrasting ideas is crucial. Language possesses a myriad of nuanced tools that enable writers to juxtapose opposing concepts, highlight disparities, and underscore points of divergence. This guide delves into an array of literary devices that serve this specific purpose, providing a comprehensive understanding of their usage and impact.1. Antithesis.Antithesis, a staple of rhetorical discourse, places two opposing ideas side by side to accentuate their contrasting nature. Its essence lies in presenting a stark contrast that draws the reader's attention to the fundamental differences between two concepts.Example: "The world is a comedy to those who think, a tragedy to those who feel." (Horace Walpole)。

The Relationship between pH and Chemical Reactions

The Relationship between pH and Chemical Reactions

The Relationship between pH andChemical ReactionsChemical reactions are an essential part of our everyday lives. They occur in nature, in our bodies, and in the products we use. The pH scale is a measure of the acidity or basicity of a solution and is an important factor in many chemical reactions. In this article, we will explore the relationship between pH and chemical reactions and how the pH of a solution affects these reactions.What is pH?The pH of a solution is a measure of the concentration of hydrogen ions (H+) in the solution. The pH scale ranges from 0 to 14, with 0 being the most acidic and 14 being the most basic. A solution with a pH of 7 is neutral, meaning it is neither acidic nor basic.Acids are substances that release hydrogen ions when they dissolve in water. The more hydrogen ions are released, the more acidic the solution becomes, and the lower the pH. Bases, on the other hand, are substances that accept hydrogen ions when they dissolve in water. The more hydrogen ions are accepted, the more basic the solution becomes, and the higher the pH.Chemical Reactions and pHThe pH of a solution can affect many different chemical reactions. For example, enzymes, which are proteins that catalyze (speed up) chemical reactions in the body, function best in a narrow pH range. If the pH of the environment is too low or too high, the enzyme may not function properly, and the reaction will not occur.Additionally, the pH of a solution can affect the solubility of certain compounds. For example, many metals are insoluble in water at low pH but become soluble at high pH. This can be important in industrial processes where metals need to be dissolved in water for further processing.Another example of how pH affects chemical reactions is in acid-base reactions. In these reactions, an acid reacts with a base to form a salt and water. The strength of the acid and base can affect the rate of the reaction. Strong acids and bases react more quickly than weak acids and bases.Acid-base reactions are important in many industrial processes. For example, in the manufacture of soap, a strong base is used to react with a fatty acid to form a soap molecule. The pH of the reaction mixture must be carefully controlled to ensure the reaction proceeds efficiently.Controlling pHControlling pH is an important part of many chemical processes. For example, in the production of beer, the pH of the mash (the mixture of malted barley and water) must be carefully controlled to ensure the enzymes in the mash function properly and break down the starches into sugars.There are several ways to control pH. One way is to add an acid or base to the solution. This is often done in industrial processes where the pH needs to be controlled very precisely. Another way to control pH is to adjust the concentration of buffering compounds in the solution. Buffers are substances that can absorb excess acid or base without significantly changing the pH of the solution.ConclusionThe pH of a solution is an important factor in many chemical reactions. It can affect the solubility of compounds, the function of enzymes, and the rate of acid-base reactions. Controlling pH is an important part of many industrial processes, and there are several ways to control pH, including adding acids or bases or adjusting the concentration of buffering compounds. The next time you see a chemical reaction, consider the role that pH might play in the process.。

英语四级作文类型总结

英语四级作文类型总结

英语四级作文类型总结In English, there are several common types of compositions that appear in the English CET-4 (College English Test Band 4) exam. Mastering these types can significantly enhance your writing skills and improve your performance on the test. Here's a summary of the main composition types:1. Descriptive Essay:This type of essay requires you to vividly describe a person, place, object, or event. You need to use sensory details to paint a clear picture for the reader and evoke emotions. Focus on using descriptive language and appeal to the reader's senses.2. Narrative Essay:In a narrative essay, you tell a story. This could be a personal experience, a fictional story, or even ahistorical event. It should have a clear beginning, middle, and end, with a central theme or message. Pay attention to storytelling techniques such as character development, plot structure, and dialogue.3. Argumentative Essay:An argumentative essay requires you to take a stance on a controversial topic and provide evidence to support your viewpoint. You should present logical arguments, cite relevant facts and statistics, and anticipate and counter opposing arguments. Structure your essay with a clear introduction, body paragraphs presenting your arguments, and a strong conclusion.4. Expository Essay:In an expository essay, you explain or inform the reader about a specific topic. This could involve defining a concept, analyzing a process, comparing and contrasting ideas, or providing a cause-and-effect explanation. Focus on presenting information in a clear, organized manner, anduse examples or evidence to support your points.5. Persuasive Essay:Similar to an argumentative essay, a persuasive essay aims to convince the reader to adopt your viewpoint or take a specific action. However, persuasive essays often rely more on emotional appeals and rhetorical devices to sway the audience. Use persuasive language, anecdotes, and appeals to ethos, pathos, and logos to strengthen your argument.6. Problem-Solution Essay:In this type of essay, you identify a problem or issue, analyze its causes and effects, and proposesolutions to address it. It's important to clearly define the problem, provide evidence of its significance, andoffer realistic and feasible solutions. Your essay should demonstrate critical thinking and problem-solving skills.7. Comparison and Contrast Essay:This essay type involves examining the similarities and differences between two or more subjects. You might compare and contrast different theories, literary works, historical events, or cultural phenomena. Organize your essay by discussing one aspect at a time and usetransitions to guide the reader through your analysis.8. Cause and Effect Essay:In a cause and effect essay, you explore the reasons why something happens (the causes) and the consequences or outcomes that result (the effects). It's important to establish clear causal relationships and support your analysis with evidence. Consider both immediate and underlying causes, as well as short-term and long-term effects.By understanding and practicing these different types of essays, you can become more proficient in expressing yourself effectively in writing and improve your performance on the English CET-4 exam. Remember tocarefully read and analyze the essay prompt, plan your essay structure, and revise and edit your writing for clarity and coherence.。

用对比法写英语作文

用对比法写英语作文

用对比法写英语作文英文回答:In the vast tapestry of human experience, the contrast between two opposing forces serves as a catalyst for growth, understanding, and enlightenment. It is through the juxtaposition of contrasting elements that we gain a deeper appreciation for their individual nuances and the intricate interplay that defines the human condition.The dichotomy between nature and civilization presentsa compelling example of this dynamic. Nature, in its untamed and awe-inspiring grandeur, embodies the raw powerof the natural world. It is a realm of untamed wilderness, tumultuous storms, and the intricate tapestry of life that thrives within its embrace. Civilization, on the other hand, stands as a testament to human ingenuity and ambition. Itis a realm of towering structures, bustling cities, and the complex systems that govern our daily lives.The juxtaposition of these two forces invites us to contemplate the delicate balance between our primalinstincts and the societal norms we have constructed. It is in the wilderness that we find solace from the demands of modern life, reconnecting with our ancestral past and the unyielding rhythms of nature. Conversely, civilization provides us with comfort, security, and the fruits of scientific and technological advancements.Another striking contrast that shapes our understanding of the world is that between war and peace. War, with its horrors and devastation, strips away the veneer ofcivilization and exposes the raw depths of human depravity. It is a time of conflict, violence, and immense suffering, leaving an enduring scar on the hearts and minds of those who experience it. Peace, on the other hand, represents a state of harmony and tranquility. It is a time of cooperation, understanding, and the pursuit of common goals.The contrast between war and peace highlights the importance of valuing human life above all else. It urgesus to seek peaceful resolutions to conflicts and to worktirelessly towards a future where dialogue and diplomacy prevail over violence and destruction. Only by understanding the full horrors of war can we truly appreciate the preciousness of peace.Another significant contrast that influences our world is that between poverty and wealth. Poverty, with its debilitating effects on individuals and communities, serves as a stark reminder of the inequalities that exist within our societies. It is a condition of deprivation, lack of opportunity, and vulnerability, leaving countless people struggling to meet their basic needs. Wealth, on the contrary, represents an abundance of resources and privileges.The contrast between poverty and wealth underscores the need for social justice and economic equality. It challenges us to examine the systems that perpetuate inequality and to work towards creating a more just and equitable society. By understanding the plight of those living in poverty, we can develop a greater sense of empathy and compassion, motivating us to advocate forchange.In the realm of the human mind, the contrast between love and hate offers a profound exploration of ouremotional spectrum. Love, with its all-encompassing warmth and unwavering devotion, represents the purest form of human connection. It is a force that brings people together, fosters understanding, and creates unbreakable bonds. Hate, on the other hand, is a destructive emotion characterizedby anger, animosity, and the desire to inflict harm.The contrast between love and hate reminds us of the transformative power of empathy and forgiveness. By cultivating love in our hearts, we can bridge divides, promote reconciliation, and create a more harmonious world. Conversely, hate only breeds division, pain, and suffering, leaving a lasting legacy of bitterness and sorrow.中文回答:自然与文明,自然代表着原始的冲动和与生俱来的本性,而文明代表着人类的智慧和野心。

The effects of pH on the properties of solvents

The effects of pH on the properties of solvents

The effects of pH on the properties ofsolvents化学实验中经常需要控制pH值,以确保反应正常进行。

不同的溶剂在不同的pH值下的性质也会出现显著的变化。

本文将探讨pH值对溶剂性质的影响。

一、溶解度溶解度是指在一定温度下,溶液中能溶解的最大量的溶质。

pH值通常直接影响溶剂中对应物质的溶解度。

例如,盐酸(HCl)是一个酸性物质。

当它被添加到水中时,会与水中的氢氧根离子(OH-)反应,生成氯化离子(Cl^-)和水分子(H2O):HCl + H2O → Cl^- + H3O+这个反应释放出氢离子(H+),这种离子在水中会与水分子结合形成氢氧根离子(OH-)。

这些反应会导致水中氢氧根离子(OH-)的浓度下降,从而缓解氯离子(Cl^-)的溶解度,使其更容易在水中形成化学化学平衡。

因此,pH值较低时,Cl^- 的溶解度更高。

二、极性pH值的变化还会影响溶剂的极性。

pH较低时,水中的氢离子浓度(H3O+)会增加,从而使水分子中的氢原子变得更加正极化(+)。

这使得水分子在pH较低的溶液中具有较高的电荷密度,从而导致水分子更加极性。

三、稳定性pH值的变化还会影响溶剂的稳定性。

根据Le Chatelier原理,当系统中发生一些变化时,系统将倾向于做出响应以抵消这些变化。

例如,当酸性物质(如盐酸)溶解在水中时,水的pH值将降低。

水中的氢氧根离子(OH^-)会与盐酸中的氢离子(H+)结合形成H2O,从而平衡这一过程。

但是,在高浓度的酸性或碱性条件下,溶液中水的分解速率会变得更快。

pH对溶液的稳定性有很大影响。

四、对化学反应的影响pH值的变化还会直接影响到化学反应的过程和效率。

许多化学反应需要特定的pH条件下才能进行。

对于酶催化反应而言,pH条件更显著。

例如,酶catalase 只在中性条件下才能正常运行。

在pH太低或太高的条件下,catalase的分子结构会发生变化,从而降低其反应效率。

英文作文中间段

英文作文中间段

英文作文中间段全文共3篇示例,供读者参考篇1The middle paragraph in an English essay is a crucial part of the overall structure and flow of the piece. It acts as the body of the essay, providing detailed information, arguments, and evidence to support the thesis statement. In this section, the writer expands on the main points introduced in the introduction and prepares the reader for the conclusion.One important aspect of a strong middle paragraph is coherence and cohesion. Each paragraph should have a clear topic sentence that introduces the main idea of the paragraph, followed by supporting sentences that provide evidence and examples to back up the claim. Transitions between sentences and paragraphs should also be smooth to ensure a seamless flow of ideas.Additionally, the middle paragraph should bewell-organized and structured. The writer should present their points in a logical order, building upon each other to create a convincing argument. This may involve using different types ofparagraph structures, such as comparison and contrast, cause and effect, or problem and solution.Moreover, the middle paragraph is an opportunity to delve deep into the topic and provide in-depth analysis. This is where the writer can showcase their understanding of the subject matter and demonstrate critical thinking skills. By presenting relevant information and evidence, the writer can persuade the reader to see things from their perspective.In conclusion, the middle paragraph is a crucial part of an English essay, providing the substance and support needed to convey the writer's message. By following the guidelines of coherence, organization, and analysis, the writer can create a compelling and well-structured piece of writing that engages the reader and effectively communicates the intended message.篇2The middle paragraph of an English essay is crucial for developing and expanding upon your main arguments. It serves as the bridge between the introduction and conclusion, providing key details, evidence, and analysis to support your thesis statement.In this section, you should delve deeper into the main points you introduced in the introduction and set the stage for the conclusion. It is important to provide detailed examples, relevant facts, and analysis to strengthen your argument and persuade the reader of your viewpoint.One effective way to structure the middle paragraph is to use the "PEE" method, which stands for Point, Evidence, and Explanation. Start by stating your main point clearly and concisely. Then, provide evidence, such as quotes, statistics, or examples, to support your point. Finally, explain how the evidence you provided supports your argument and ties back to your thesis statement.Additionally, it is important to ensure smooth transitions between paragraphs in the middle section of your essay. Use transition words and phrases to connect ideas and guide the reader through your argument seamlessly. Some examples of transition words include "furthermore," "moreover," "in addition," and "however."Overall, the middle paragraph is where you can really delve into the meat of your argument and provide the necessary evidence and analysis to support your claims. Make sure to be thorough in your research, provide strong evidence, and clearlyexplain how it all ties back to your thesis statement. By following these guidelines, you can craft a strong and persuasive middle paragraph that will effectively support your overall argument in an English essay.篇3The middle paragraph is the core of an English essay. It is where the main argument is developed, supported, and elaborated upon. In this section, the writer presents their main ideas and provides evidence to back up their claims. It is crucial to ensure that the middle paragraph is well-structured and organized, with a clear and logical flow of ideas.To begin with, the middle paragraph should start with a topic sentence that introduces the main argument or point of the paragraph. This sentence should be concise and straightforward, setting the tone for the rest of the paragraph. The topic sentence acts as a guide for the reader, helping them understand what the paragraph is about and what to expect.After the topic sentence, the writer should provide evidence to support their argument. This evidence can take many forms, such as facts, statistics, examples, or quotes from experts. It isessential to ensure that the evidence is relevant and credible, helping to strengthen the writer's argument.Next, the writer should analyze and interpret the evidence, showing how it supports their main argument. This analysis should be thorough and detailed, demonstrating a clear understanding of the evidence and its implications. By providing a thoughtful analysis, the writer can further convince the reader of the validity of their argument.Additionally, the writer should consider including counterarguments in the middle paragraph. Addressing potential objections or opposing viewpoints can help strengthen the writer's argument by showing that they have considered other perspectives and still maintain their position. By acknowledging and refuting counterarguments, the writer can demonstrate their critical thinking skills and strengthen their argument.Finally, the middle paragraph should end with a concluding sentence that summarizes the main points of the paragraph and transitions smoothly to the next paragraph. This sentence should tie back to the topic sentence and reinforce the main argument of the paragraph. By providing a strong conclusion, the writer can ensure that their argument is cohesive and well-supported.In conclusion, the middle paragraph is a crucial part of an English essay, where the main argument is developed and supported. By following the guidelines outlined above, writers can create strong, well-structured middle paragraphs that effectively convey their ideas and persuade readers of their argument.。

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Geosciences JournalVol. 7, No. 2, p. 163 167, June 2003Comparison of pH and counter-ion effect in surfactant-assisted remediationABSTRACT: In order to determine whether pH or counter-ion is more effective in modifying surfactant effectiveness, column exper-iments were performed. Ottawa sand was selected for model soil and toluene was used as a model contaminant. DOSL (anionic sur-factant) was used for this study. The greatest recovery of toluene in column tests was 92%, which was obtained with a surfactant + NaOH. The effect of NaCl in changing effectiveness was less than that of NaOH. Much greater effectiveness was observed using sur-factant solutions containing NaOH. The effect of NaOH in chang-ing effectiveness was not due to Na+ effects, but to the OH− as shown by these experimental results. The effect of counter-ion (Na+) was small, and was much less than that of pH in surfactant-assisted remediation.Key words: pH, counter-ion, surfactant, recovery, toluene, remediation 1. INTRODUCTIONContamination of soils and groundwater with hydropho-bic chemicals is a widespread problem. The removal of hydrophobic organic substances from contaminated soils and groundwater is difficult because of low solubilities and high interfacial tensions (Sabatini et al., 1997, Lee et al., 2001a). A common method for remediation of aquifers con-taminated with hydrophobic organic substances is pump-and-treat. This method is neither effective nor economical. An extensive study on soil and groundwater remediation has demonstrated that surfactant (surface active agents) flushing is a viable alternative for improving the efficiency of pump-and-treat remediation (Pennell et al., 1997, Lee et al., 2001a, 2002a). These studies show that aqueous sur-factant solutions significantly enhance the removal of hydrophobic contaminants from soil and groundwater. Surfactants have the ability to both solubilize hydropho-bic substances and to lower interfacial tensions and increase mobility of the contaminants. However, surfactant-based technologies are still ineffective on silts and clays due to their small particle size and large specific surfaces. Further, aqueous surfactant solutions are affected by environmental conditions such as pH, counter-ion conditions, temperature, and the clay type and percentage etc. Rosen (1989) and Harwell (1992) observed that micelle formation of surfac-tant is also enhanced by high pH conditions. Chang and Rosano (1984) reported that generally the higher pH, the lower surface tension of a surfactant solution. Lee et al. (2002b) suggested that the effect of electrolyte of target area in surface-based remediation should be considered for remediation design. The addition of an electrolyte such as NaCl to an anionic surfactant solution can both increase the micelle aggregation number (size of micelle) and decrease the CMC (Hiemenz, 1986), thereby modifying surfactant effectiveness for remediation. The addition of NaOH for pH adjustment adds two ions, Na+ and OH−, to the surfactant solution. Changes in effectiveness for remediation could be caused either by pH changes or by changes on the counter-ion Na+. More laboratory work and/or pilot scale tests are needed to understand the modifying surfactant effective-ness. In order to determine whether OH− or Na+ more effec-tive in modifying surfactant effectiveness, experiments were performed with electrolyte (NaCl, NaOH) added to the surfactant solutions.2. MATERIALS AND METHODS2.1. MaterialsMaterials used as model soil require high permeability, low cation exchange capacity, and low total organic carbon content. Ottawa sand was selected because it met these cri-teria, and because of its uniformity, simple mineralogy, and availability. It was obtained from the U.S. Silica Company (Ottawa, IL, USA). The mean grain diameter of Ottawa sand is 0.45mm, and the specific surface area is 0.007m2/g (Lee, 1999). Ottawa sand was washed with deionized water to remove fine materials and air dried prior to use. Toluene (C6H5CH3) was used for the model contamina-tion. Toluene (reagent grade), a non-chlorinated aromatic hydrocarbon, is a major industrial hydrophobic organic compound and is commonly found at waste disposal sites. It is similar to benzene but is less toxic. Toluene is com-pletely soluble in organic solvents such as hexane so that it can be easily extracted. It was obtained from Fisher Scien-tific (Chicago, IL, USA). The characteristics of toluene are shown in Table 1.4% (v/v) DOSL (Dowfax 8390 anionic surfactant) was selected for this study. Surfactant concentration of 4% (v/v) provides the best removal efficiency in a previous study (Lee, 1999). DOSL has good solubilizing abilities forDal-Heui Lee*Jong-Sik RyuEun-Sik Kim}School of Earth and Environmental Sciences, Seoul National University, Seoul 151-747, Korea *Corresponding author: dhlee44@snu.ac.kr164Dal-Heui Lee, Jong-Sik Ryu and Eun-Sik Kimhydrophobic organic molecules (Rouse et al., 1993). Anionic surfactants are usually chosen for surfactant-based remedi-ation procedures because of their lower degree of adsorp-tion on soil than that by cationic and nonionic surfactant (Lee et al., 2002b). DOSL (sodium diphenyl oxide disul-fonate) was obtained Dowfax Chemical (Midland, MI, USA)and meets criteria as an indirect food additive under U.S.Food and Drug Administration (FDA) (Regulation 21CFR-178.3400) and is rapidly biodegradable by soil and/or aquatic microorganisms. The characteristics of DOSL are shown in Table 2.2.2. MethodsThe glass column used in this study was 5cm (O.D.) in diameter and 30 in height. This column was obtained from Supelco Company. Experimental methods and procedures were similar to those performed in prior research (Lee et al.,2001b). Glass wool and glass beads were placed at the col-umns base, and 350 g of Ottawa sand was placed over the beads. Compaction of the dry soil in 0.5cm layers was standardized by tapping the side of the column 25 times.After a column was packed, deionized water was pimped ata rate of 4ml/min into the column for 3 hours to saturate the soil (Fig. 1). The contaminant (5ml of toluene) was then injected by syringe into the upper middle of the col-umn, which is a method of contamination analogous to a point source of contamination at the field scale. Then 4%(v/v) surfactant solutions with/without 2% NaCl or deion-ized water was pumped into the columns top at a rate of 4/min. The same number of Na + moles were added as those from NaOH in this experiments (Lee et al., 2001a, b). In order to evaluate the effects of pH on surfactant-based lab-scale remediation, the pH of surfactant solutions was varied by adjusting pH with a 10% NaOH (2.5 M) solution. pH values of the 4% (v/v) DOSL solutions were adjusted to 10based on prior study (Lee et al., 2002a, b). Effluent was col-lected in 5 individual 250ml fractions to give a total vol-ume of 1250ml. Each treatment was evaluated in duplicate columns.2.3. Analytical MethodsToluene in aqueous samples was extracted by solvent extraction with hexane using standard separatory funnel method 3510 (Lee, 1999; Lee et al., 2001b) and analysed by gas chromatography with split/splitless injection system (Hewlett Packard Model 5890 series II) (Lee, 1999). The solid samples were extracted using a soxhlet extractionTable 1. Characteristics of model organic contaminant Toluene a FormulaC 6H 5CH 3Molecular weight 92.1Liquid density (g/cm 3)0.87Aqueous solubility b (mg/l)510Log octanol-water partition coefficient 2.69Liquid-air interfacial tension (dyne/cm)29Liquid-water interfacial tension (dyne/cm)36Total gas density (kg/m 3) 1.27Viscosity (cP)0.9a Data from Fisher Scientific, Chicago, IL.b20−25o C, atmospheric pressure.Table 2. The Characteristics of used surfactant.Trade NameDOSL (Dowfax 8390)Chemical name Diphenyl oxide disulfonates Molecular weight 642HLBa13CMC b(mM)0.5Molecular formula C 16H 33C 12H 7O(SO 3Na)2Type Anionic Company Dow Chemical, Midland, MI Water solubility Completely miscible Specific gravity 1.03−1.13Data come from manufacturers.aHLB =hydrophile-lipophile balance.bCMC =critical micelle concentration.Fig. 1. Schematic diagram of continuous leaching experimental apparatus.Comparison of pH and counter-ion 165method. Prior to the analysis of the extracted samples, the response factor and linearity of detection for the internal standard and contaminant were determined. After calculat-ing the response factor, a calibration graph was prepared.The quantitative determination of contaminant concentra-tion was based on these internal standard reference com-pounds, so that sample peak areas were compared with those of their respective internal standards (ethylbenzene for toluene) (Lee, 1999).3. RESULTS AND DISCUSSIONFigure 2 and Table 3 show the effect of NaOH in removal effectiveness of toluene. The increase was 16% for anionic DOSL, 12% for anionic Sandopan JA36 (Lee et al., 2001a),and 9% for the nonionic Triton X100 (Lee et al., 2001a).This increase was much less than that observed for another sand column experiments (Lee, 1997, 1999). In this study,much greater effectiveness was observed using surfactant solutions containing NaOH. NaOH increased the effective-ness of a nonionic surfactant (Pluronic L44) by 50%, an anionic surfactant (Sandopan JA36) by 57%, and water by 10% in a pure sand column. The model contaminant was toluene in this study (Lee, 1997). Also, monitored pH val-ues of effluent solutions during experiments were almost same as the initial solution pH at the start of each test.Chang and Rosano (1984) and Rosen (1989) found that micelle formation in surfactant solutions was enhanced by high pH conditions and the surface tension of surfactant solutions was decreased by high pH. Both factors may have affected our results. However, the cause of lesser affects compared to Lee’s (1997) results is not known althoughprobably resulted from the different model surfactants.Hydrogen ion concentration in solution was an important factor in surfactant effectiveness (Rosen, 1989). Figure 2shows that DOSL surfactant solution with NaOH affects clearly toluene removal from contaminated soil columns.The addition of small amounts of pH neutral electrolyte such as NaCl to an anionic surfactant solution can both increase the micelle aggregation number (size of micelle)and decrease the CMC (Critical Micelle Concentration),thereby modifying surfactant effectiveness for remediation (Harwell, 1992). Also Rosen (1989) showed that the addi-tion of small amounts of pH neutral electrolyte to solution of ionic surfactants appears to increase the extent of solu-bilization of hydrocarbons that are solubilized in the inner core of the micelle. Increased binding of cations (Na +)should cause the CMC of the surfactant to decrease and the aggregation number to increase with the stabilization of micelles. Therefore, experiments were conducted to exam-ine the effect of cations (Na +) in the removal toluene from the Ottawa sand. Figure 3 and Table 4 show the effect of NaCl in removal effectiveness of toluene. In contrast, Na +as 2% NaCl (wt NaCl per volume solution) had almost no effect on DOSL effectiveness compared to surfactant solu-tions without the added NaCl. We should also point out thatFig. 2. Effect of NaOH on leaching of toluene from sand.T able 3. The effect of 10% NaOH (2.5M) in removal (%) of toluene.Surfactant Without NaOH With NaOH EffectivenessDOSL799216% increase Sandopan JA36*748312% increase Triton X100*74819% increase*from Lee et al. (2001a)166Dal-Heui Lee, Jong-Sik Ryu and Eun-Sik KimDOSL is considered as a low Na+ surfactant containing about 0.1%−0.3% NaCl (Rouse et al., 1993) so that counter-ion effects of Na+ from the DOSL itself should be very minor. The effect of Na+ was small, and was much less than that of pH (Table 5). The effect of NaOH in changing effec-tiveness is not due to Na+ effects, but rather to the OH− as shown by these experimental results.Based on results of these column tests, DOSL with elec-trolyte (especially NaOH) can be a good candidate for sur-factant-assisted soil or groundwater remediation. In addition to the high percentage removal of toluene observed in our column experiments, DOSL has good solubilizing abilities for 1,2,4-trichlorobenzene, phenanthrene, naphthalene and related substances (Deshpande et al., 2000). Also, DOSL should show minimal loss during surfactant flushing because of low sorption to soil particle and resistance to precipita-tion with cations (Na+).4. CONCLUSIONS1) Much greater effectiveness was observed using sur-factant solutions containing NaOH. 2) The effect of NaCl in changing effectiveness was less than that of NaOH. 3) The effect of NaOH in changing effectiveness was not due to Na+ counter-ion effects, but rather to the OH−. Subsur-face aquifers will rarely contain such high pH waters, and buffering of pH in surfactant solutions to pH 10 may prove difficult and expensive for many aquifers. If possible, how-ever, maintaining a high pH surfactant solution in field remediation is desirable because it will enhance contami-nant removal.Fig. 3. Effect of NaCl on leaching of toluene from sand.Table 4. The effect of 2% NaCl in removal (%) of toluene.Surfactant Without NaCl With NaCl EffectivenessDOSL8080No increaseSandopan JA36*75795% increaseTriton X100*75761% increase*from Lee et al. (2001a)Table 5. Comparison of NaOH and NaCl removal (%) effect in surfactant-based remediation.NaOH or NaCl DOSL (anionic)Sandopan JA36 (anionic)Triton X100 (nonionic) Unadjusted pH and without NaCl797474pH 10 with NaOH and without NaCl928381pH 11 with NaOH and without NaCl c888180pH 10 with NaOH and with NaCl a,c897976pH 11 with NaOH and with NaCl b,c857976a++b Na+ from NaCl equivalent to pH 11 Na+ in NaOHc from Lee (1997, 1999)Comparison of pH and counter-ion167ACKNOWLEDGMENTS: We would like to thank Dr. R.D. Cody of Iowa State University, U.S.A. for the discussion. Authors also express appreciation to the members of the Environmental Geochemistry Labo-ratory, Seoul National University, Korea. This study was supported by the BK21 project, Ministry of Education.REFERENCESChang, D.L. and Rosano, H.L., 1984, Interaction of long chain dim-ethylamine oxide with sodium dodecyl sulfate in water. ACS Symposium Series 129, 129−140.Deshpande, S., Shiau, B.J., Wade, D., Sabatini, D.A. and Harwell, J.H., 2000, Dowfax surfactant components for enhancing con-taminant solubilization. Water Research, 34, 1030−1036. Harwell, J.H., 1992, Factors affecting surfactant performance in groundwater remediation applications. ACS Symposium Series 491, 124−131.Hiemenz, P.C., 1986, Principles of colloid and surface chemistry, 2nd ed. New York, Marcel Dekker Inc., p. 427−488.Lee, D.-H., 1997, The effect of surfactants in leaching hydrophobic organic compounds from sand. M.S. thesis, Iowa State Univer-sity, Ames, USA, 88 p.Lee, D.-H., 1999, Experimental investigation of the removal of hydrophobic organic compounds from two Iowa soils using food grade surfactants and recovery of used surfactants. Ph.D. Disser-tation, Iowa State University, Ames, USA, 200 p.Lee, D.-H., Cody, R.D. and Hoyle, B.L., 2001a, Laboratory evalua-tion of the use of surfactant for groundwater remediation and the potential for recycling them. Ground Water Monitoring andRemediation, 21, 49−57.Lee, D.-H., Cody, R.D. and Hoyle, B.L., 2001b, Comparison of six surfactants in removing toluene and trichlorobenzene from a sandy soil under laboratory conditions. Canadian Geotechnical Journal, 38, 1329−1334.Lee, D.-H., Cody, R.D. and Kim, D.-J., 2002a, Surfactant recycling by solvent extraction in surfactant-aided remediation. Separation and Purification Technology, 27, 77−82.Lee, D.-H., Cody, R.D. and Kim, D.-J., 2002b, Choi, S.C., 2002b, Effect of soil texture on surfactant-based remediation of hydro-phobic organic-contaminated soil. Environment International, 27, 681−688.Pennell, K.D., Adinolfi, A.M., Abriola, L.M. and Diallo, M.S., 1997, Solubilization of a dodecane, tetrachloroethylene, and 1,2-dichlo-ribenzene in micellar solutions of ethoxylated nonionic surfac-tants. Environmental Science and Technology, 31, 1382−1389. Sabatini, D.A., Knox, R.C., Harwell, J.H., Soerens, T., Chen, L., Brown, R.E. and West, C.C., 1997, Design of a surfactant reme-diation field demonstration based on laboratory and modeling studies, Ground Water, 35, 954−963.Rosen, M.J., 1989, Surfactants and interfacial phenomena. John Wiley & Sons, New York, 431 p.Rouse, J.D., Sabatini, D.A. and Harwell, J.H., 1993, Minimizing sur-factant losses using twin-head anionic surfactants in subsurface remediation. Environmental Science and Technology, 27, 2072−2078.Manuscript received August 27, 2002Manuscript accepted March 30, 2003。

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