sdarticle(1)

合集下载

期刊索引

期刊索引

Elsevier ScienceDirect(SD)荷兰Elsevier Science 出版集团出版的期刊是世界上公认的高质量学术期刊,其中大部分期刊被S CI、SSCI、EI所收录。

目前其SDOS(Science Direct Onsite)网络全文数据库包括1995年以来Es evier Science 出版的1800余种高品质全文学术期刊,涵盖了生命科学、计算机科学、工程、环境科学、农业和生物科学、数学、经济、商业、管理、社会科学、艺术和人文科学等23个学科领域。

SD收录的图书不在图书馆购买范围之内,因此不能阅读、下载SD的图书。

Web of Science数据库Web of Science是美国Thomson Scientific(汤姆森科技信息集团)基于WEB开发的产品,是大型综合性、多学科、核心期刊引文索引数据库,包括三大引文数据库(科学引文索引(Science Citation Index,简称SCI)、社会科学引文索引(Social Sciences Citation Index,简称SSCI)和艺术与人文科学引文索引(Arts & Humanities Citation Index,简称A&HCI))和两个化学信息事实型数据库(C urrent Chemical Reactions,简称CCR和Index Chemicus,简称IC),以及科学引文检索扩展版(S cience Ciation Index Expanded,SCIE)、科技会议文献引文索引(Conference Proceedings Citation Index-Science,CPCI-S)和社会科学以及人文科学会议文献引文索引(Conference Proceedings Ci tation index-Social Science&Humannalities,CPCI-SSH)三个引文数据库,以ISI Web of Knowledge作为检索平台。

英文作文article

英文作文article

英文作文articleTitle: The Impact of Technology on Education。

In today's rapidly evolving world, technology plays an increasingly significant role in every aspect of our lives, including education. The integration of technology into education has brought about both positive and negative impacts, shaping the way students learn and educators teach. This article explores the various ways in which technology influences education and discusses its implications for the future.First and foremost, technology has revolutionized the way information is accessed and disseminated. With the internet and digital devices, students now have access to a vast amount of information at their fingertips. They can easily conduct research, explore diverse perspectives, and engage with multimedia resources to enhance their learning experience. This accessibility to information has democratized education, breaking down barriers to learningand empowering students from all backgrounds to pursue knowledge.Moreover, technology has transformed the traditional classroom environment. Interactive whiteboards, educational apps, and online platforms have become commonplace, providing educators with tools to create dynamic and engaging lessons. These digital resources cater todifferent learning styles and allow for personalized instruction, enabling students to learn at their own pace and according to their individual needs. Additionally, technology facilitates collaboration among students through online forums, video conferencing, and shared documents, fostering a sense of community and enhancing communication skills.Furthermore, technology has opened up new avenues for creativity and innovation in education. Students can now utilize multimedia tools to express their ideas, create multimedia presentations, and develop digital projects. Virtual reality (VR) and augmented reality (AR) technologies offer immersive learning experiences, allowingstudents to explore virtual environments and simulate real-world scenarios. These innovative approaches not only make learning more engaging but also cultivate critical thinking, problem-solving, and digital literacy skills essential for success in the 21st century.However, despite its numerous benefits, the widespread use of technology in education also poses challenges and concerns. One major issue is the digital divide, whichrefers to the gap between those who have access to technology and those who do not. Socioeconomic disparities and inadequate infrastructure can hinder access to digital devices and high-speed internet, depriving certain students of the opportunities afforded by technology. Bridging this divide requires concerted efforts from policymakers, educators, and technology providers to ensure equitable access to technology for all students.Additionally, the overreliance on technology in education raises concerns about its potential drawbacks. Excessive screen time and digital distractions can impede students' focus and concentration, leading to decreasedacademic performance and impaired social skills. Moreover, the proliferation of online resources raises questions about the quality and credibility of information available to students. Educators must teach students how tocritically evaluate sources and discern fact from fiction in an age of information overload.In conclusion, technology has undoubtedly reshaped the landscape of education, offering unprecedentedopportunities for learning and innovation. From enhancing access to information to fostering collaboration and creativity, technology has the potential to revolutionize education for the better. However, realizing this potential requires addressing challenges such as the digital divide and mitigating the risks associated with overreliance on technology. By harnessing the power of technology responsibly, educators can empower students to thrive in a digital age and prepare them for the challenges of the future.。

U2T1SD

U2T1SD

Section DⅠ. Material analysis本课是第二单元第一话题的第四课时,主活动是1a和Project。

通过Grammar 来巩固总结一般过去时和现在完成时的区别,通过Functions 来复习重要的表达法。

1a按照“总—分—总”的模式分别介绍了各种污染的成因及危害。

通过完成文章后的表格,训练和提高学生获取信息的能力。

教师还可以利用表格内容,引导学生整合信息复述课文,巩固课文内容。

1b属于同义转换练习。

Project部分培养学生动手动脑的能力,让学生运用收集的信息和所学知识,通过墙报的形式来宣传污染带来的危害,让更多的人关注环境污染,树立环保意识,增强人们的忧患意识和社会责任感。

Ⅱ.Teaching aims1.Knowledge aims:掌握本课的重点词汇和短语。

总结一般过去时和现在完成时的区别;复习本话题的重点表达法。

2.Skill aims:能读懂与环境污染问题有关的文章。

能根据关键词复述课文。

3. Emotional aims: (optional)通过了解各种污染带来的危害,帮助学生树立环保意识,爱护环境,保护地球。

14.Culture awareness: (optional)通过学习,引导学生了解环境污染对人类健康有巨大的危害,不同种类的污染体现在不同的方面。

Ⅲ. The key points and difficult points1. Key points:Words and phrases: coal, create, blood, planet, in many ways, with the development of industry, high blood pressure Grammar: the differences between the simple past and present perfect2. Difficult points:能根据关键词复述课文。

sdarticle11

sdarticle11

annual volatilities of spot prices were 163.91% for copper, 119.05% for chromium, 168.24% for uranium, 153.87% for zinc, and 44.46% for lead. These data show that increasingly more companies are being exposed to high risks in natural resources prices, implying that the stable supply of natural resources is very important for the national economy and for the survival of a company.
1216
C. Won / Energy 34 (2009) 1215–1224

pricing model which is both easy to apply and realistic in order to help firms’ investment decision-making.
There are two major competing procedures for evaluating risky projects in natural resources developments: one is decision analytic, based on traditional discounted cash flow and stochastic dynamic programming (Fleten et al. [11], Smith and McCardle [27], Szklo et al. [28]) and the other is option pricing model (OPM) or contingent claims analysis, based on the no-arbitrage theory of financial markets (Brennan and Schwartz [3], Ekern [9], Emhjellen and Alaouze [10], Laughton [18], Paddock et al. [22], Schwartz [25], Sezgen et al. [26]). In this paper, we develop a new pricing model of natural resources projects by applying contingent claim analysis in order to help firms evaluate the projects more accurately and easily. Our model is different from previous models in several respects. First, our model uses different assumptions about underlying variables and different methodology. For example, we treat both output prices and development costs as stochastic and derive a closed-form solution through Martingale framework. While most of the previous literature treats only output prices as stochastic (Brennan and Schwartz [3], Dixit [6], Gibson and Schwartz [14], Laughton [18], Paddock et al. [22], Pindyck [23], Schwartz [24, 25], Sezgen et al. [26]) and does costs as uncertain, we make our model more realistic by treating both output prices and development costs as stochastic processes, because development costs change over time depending upon the fluctuations in materials and labor costs necessary for the developments. In addition, whereas we utilize Martingale principle to derive the pricing equation, other authors use different methods, such as an arbitrage argument through self-financing (Brennan and Schwartz [3]), a dynamic decision tree (Smith and McCardle [27]), and a real option framework by considering various managerial flexibility in the process of developments (Cortazar and Casassus [5], Fleten et al. [11], Laughton [18], Olsen and Stensland [21], Paddock et al. [22], Sezgen et al. [26], Szklo et al. [28]).

research article 中各部分的内容和作用

research article 中各部分的内容和作用

research article 中各部分的内容和作用
在Research Article中,通常包含以下几个部分,这些部分各自具有其特定的内容与作用:
1. 摘要(Abstract):摘要部分通常简明扼要地概括了研究的主要内容、方法、结果和结论。

它为读者提供了关于研究的快速概览,帮助读者决定是否需要进一步阅读整篇文章。

2. 引言(Introduction):引言部分详细介绍了研究的背景和目的,为理解后续的研究内容提供了背景信息。

它解释了为什么这个研究是重要的,以及预期的研究结果如何影响该领域的知识。

3. 方法(Methods):这一部分详细描述了用于收集数据或执行实验的程序和过程。

它确保其他研究人员能够复制并验证研究结果。

4. 结果(Results):结果部分呈现了通过研究获得的数据。

这些数据通常以图表、表格等形式呈现,以便读者可以直观地理解。

5. 讨论(Discussion):在讨论部分,研究人员会解释研究结果的含义,将其与之前的研究进行比较,并探讨可能的解释和局限性。

此外,他们通常也会提出对未来研究的建议。

6. 结论(Conclusion):结论部分总结了研究的主要发现,并强调这些发现对领域的影响和贡献。

它也指出了研究的局限性和未来可能的研究方向。

以上是Research Article中常见的各个部分的内容和作用。

具体组成部分可能会根据研究领域和期刊的要求有所不同。

在撰写Research Article时,遵循期刊的格式和结构要求是非常重要的。

sdarticle11

sdarticle11

Effect of shearing on crystallization behavior ofpoly(ethylene naphthalate)W.J.Yoon,H.S.Myung,B.C.Kim,S.S.Im *Department of Textile Engineering,Hanyang University,Haengdang,Seongdong,Seoul 133-791,South KoreaReceived 11August 1999;received in revised form 24September 1999;accepted 30September 1999AbstractThe effect of shear history on the isothermal crystallization behavior of poly(ethylene naphthalate)(PEN)was investigated by rheological and morphological measurements.Time sweep measurements of storage modulus (G H )and dynamic viscosity (h H )were carried out on the molten PEN by Advanced Rheometric Expansion System (ARES)in the parallel-plate geometry at several different temperatures and frequencies,followed by structural analysis by differential scanning calorimeter (DSC),X-ray diffractometer,and polarizing microscopy for the shear-induced crystallized PEN specimens in the ARES measurements.The rate of isothermal crystallization of PEN was notably affected by temperature,while the shear rate has an important effect on the structures of the resultant crystals.At a constant shear rate,the rate of crystallization by shear-induced structuring mechanism was increased with lowering temperature over the temperature range 230–250ЊC.The rate of crystallization was increased with increasing shear rate at a given temperature.An increase in shear rate increased both nucleation and number of crystallites.Further,it increased the content of the a -form crystal in the specimen.On the other hand,lower shear rate offered more favorable conditions for forming the b -form crystal.DSC analysis exhibited that the b -form crystal had higher melting temperature (T m )than the a -form crystal.The wide angle X-ray diffraction (WAXD)patterns also ascertained that higher content of the a -form crystal was produced in the PEN specimen crystallized at higher frequency.᭧2000Elsevier Science Ltd.All rights reserved.Keywords :Poly(ethylene naphthalate);Rheology;Shear-induced crystallization1.IntroductionShear-induced structural changes in polymeric materials take an increasing interest in the field of polymer proces-sing.In real polymer processing very complex deformation histories are involved,which can influence ultimate proper-ties of plastics.Recent advances in experimental techniques that allow in situ measurements of materials under deforma-tion have escalated research in this subject area.It has been known for a long time that flow stress have accelerating effect on the crystallization of semi-crystalline polymers [1–6].It is supposed that the application of a shear stress to a polymer melt should lead to formation of orientation and reduce the entropy of the melt,which results in a higher melting temperature and,hence,lead to an increased super-cooling [3,7].Several experiments have been described in the literature where attempts were made to quantify the shear stress-induced crystallization in molten semi-crystal-line polymers such as polypropylene [3,8,9],polyethylene oxide [10],polypropylene [11–13],and polybutene-1[3,14].Some investigators used rotational viscometers andmeasured either the volume change [15]or the number of nuclei formed during shearing [11,14].The polymers enum-erated above are apt to process because of low melting point and viscosity.On the other hand,PEN has good thermal and mechanical properties and is being used as engineering plastics.PEN is reported to have two different triclinic crystalline structures,a -form and b -form crystals.Of two crystal forms,the b -form crystal is known to be more stable than the a -form.The effect of crystallization temperature on the resultant crystal structure is well recognized;lower temperature favors formation of the a -form crystal.The critical temperature is reported about 230ЊC.However,the effect of shear history on the crystal structure of PEN has not been reported.In this study,the shear-induced crystallization behavior of PEN was investigated on the rheological basis.The effect of shear history on the crystalline structure was also discussed in terms of thermal and morphological properties.2.Experimental 2.1.MaterialThe PEN tested was a commercially available gradePolymer 41(2000)4933–49420032-3861/00/$-see front matter ᭧2000Elsevier Science Ltd.All rights reserved.PII:S0032-3861(99)00703-X*Corresponding author.Tel.:ϩ82-2-2292-0495;fax:ϩ82-2-2297-5859.E-mail address:imss007@email.hanyang.ac.kr (S.S.Im).supplied by Kolon Group in South Korea.The inherent viscosity,0.344dl/g was determined in a mixture of trifluoroacetic acid and chloroform (1/3v/v%)with an Ubbelohde viscometer at 25^0:1ЊC :The polymer was dried in a vacuum oven at 120ЊC for 24h prior to use.2.2.Measurement of physical propertiesThe dynamic rheological properties were measured by ARES (Rheometric Scientifics)in the parallel plate geome-try.The plate diameter was 12.5mm,strain level was 5%,and gap between the plates was 1mm.The PEN chips were melted at 300ЊC.The initial gap was set to a value equiva-lent to final gap plus 50m m.The excess sample squeezed out by reducing the gap was carefully trimmed off.The value was reset to the final gap value,1mm.To remove the residual stress the newly set PEN specimen was relaxed for about 5min at the temperature in nitrogen atmosphere,then cooled to the predetermined temperature for rheologi-cal measurements.A time-sweep experiment was continued for the specimen till the G H reached the ceiling value of the apparatus.After ARES measurement,the molten PEN sample was detached from the plates for measuring other properties such as thermal and morphological properties by DSC,X-ray diffractometer and polarizing optical micro-scopy.Thermal properties were measured by Perkin–Elmer DSC-7over the temperature 50–300ЊC at the heating rate of 10ЊC/min under nitrogen purge.The isothermalcrystallization experiment was performed by two different methods.Firstly,the PEN sample was heated to 300ЊC at the heating rate of 200ЊC/min,and held for about 5min,then they were cooled to the preset temperature to bring about the isothermal crystallization for same time required in ARES experiment.Secondly,the PEN chips were melted at 300ЊC between two slide glasses for 5min on the hot stage.They were moved to an oil bath very quickly and isothermally crystallized at 230,240,and 250ЊC for 4,10,and 24h,respectively.Wide angle X-ray diffraction patterns of the isothermally crystallized PEN specimen in the oil bath and ARES were obtained by X-ray diffractometer (Rigaku Denki)with Ni-filtered CuK a radiation at 35kV and 35mA.Morphology of quiescent and shear-induced crystallized PEN specimen was observed by polarized microscopy (Nikon HFX-IIA).The spherulite structure was observed by microtoming the specimen.3.Results and discussionIn the plot of G H and h H versus time at a given frequency for a polymer,the two parameters may give information on the change in physicochemical properties of the polymer.For thermally sensitive polymer melts,an irreversible decrease of viscosity with time at a constant shear rate suggests the possibility of thermal degradation of polymer molecules,whereas an irreversible increase of viscosityW.J.Yoon et al./Polymer 41(2000)4933–49424934Fig.1.Variation of G H with time for PEN melt at 240ЊC at three different frequencies.with time indicates the possibility of chemical crosslinkingbetween polymer molecules.Both thermal degradation andchemical crosslinking show irreversibility in the rheologicalresponses.On the other hand,a reversible change in G H and h H with time at a constant frequency may be caused by changing in the physical state of the polymer melts.A typi-cal example of the physical change is the isothermal crystal-lization.As the crystallites grow to larger sized spheruliteswithin the PEN melt through nucleation and growth,thehomogeneous melt system changes to the heterogeneoussystem.Thus the G H and h H increase with the crystallization time.Figs.1and2show the variation of the G H and h H of PEN melt with time at240ЊC at three different shear rates(1,3, and5rad/s).At the early stage of experiment,both G H and h H are increased slowly,indicating an induction time for crystallization.The induction period is the stage when randomly entangled polymer chains transform to the regular aligned lattice.Because of topological obstruction of such entanglements,the polymer crystallization is extremely slow[16].However,an abrupt increase of both parameters follows in some minutes.This phenomenon can be ascribed to the formation of tiny crystals so-called crystallites prob-ably due to shear-induced crystallization.It can be easily imagined that the homogeneous PEN melt changes to a suspension system with proceeding crystallization,in which numerous crystallites are dispersed in the homo-geneous molten polymer matrix.The viscosity increases due to increasing the volume fraction of dispersed crystal-lites with progressing crystallization,which is also reportedby others[7,9,11,14,17].The ceiling value of G H is the same regardless of frequen-cies and temperatures whenfinishing crystallization asshown in Fig.1.On the other hand,the ceiling value of h H is gradually decreased with increasing the applied frequency as shown in Fig.2.This is attributable to pseudo-plasticity.That is,the heterogeneous system is expected toshow yield behavior[18].At low shear rates the hetero-geneous systems exhibit very high viscosity,and almostunbounded viscosity at zero shear rate.The viscosity,however,is rapidly decreased if the shear rate exceeds acritical value.Consequently,the ceiling viscosity at1rad/sis greater than at5rad/s.In addition,the ceiling value of h H shows a gradual decrease with time after having reached maximum as shown in Fig.2,which is more noticeable at the higher frequency.The gradual decrease of h H seems to result from the restructuring of the heterogeneous systems. That is,the viscosity is decreased with shearing on account of destruction of the orderedfiller particle structure.The destruction of the pseudostructure offiller particles is increased as shear rate is increased.Fig.2reflects this.It is also noted in Figs.1and2that the induction time forcrystallization is decreased as frequency is increased.Anapplication of shear stress to a polymer melt would giverise to two characteristic responses,orientation and slippageof polymer molecules.They are associated with theW.J.Yoon et al./Polymer41(2000)4933–49424935Fig.2.Variation of h H with time for PEN melt at240ЊC at three different frequencies.W.J.Yoon et al./Polymer41(2000)4933–49424936Fig.3.Variation of G H(A)and h H(B)for PEN melt at3rad/s at three different temperatures.W.J.Yoon et al./Polymer41(2000)4933–49424937Fig.4.DSC thermograms of PEN isothermally crystallized at(A)230ЊC,(B)240ЊC and(C)250ЊC at various frequencies.macroscopic phenomena of elasticity and flow,respectively.That is,the oriented polymer molecule has fewer possible conformations than the unoriented one,which results in lower entropy.At the melting temperature,the free energy of the crystal equals the free energy of the melt as written by [3]T mD H f D S f H m ϪH cS m ϪS c1Hence,for an oriented melt,the ensuing reduction in entropy raises T m .Further,it increases the degree of super-cooling,accelerating the rate of crystallization.In general,higher shear rate gives better chance for orientation.Con-sequently,the induction time for cystallization is decreased with increasing shear rate.In Fig.3(A)and (B)shows that the annealing temperaturehas a profound effect on the nucleation and crystallization mechanism of PEN melts.The increase of G H and h H with annealing time represents the extent of crystallization of the melts with annealing time.Fig.3suggests that the number and growth rate of the nucleated crystallites is greater at 230ЊC than at 250ЊC.That is,both nucleation density and growth rate of crystallites are diminished with raising the annealing temperature.This stands to reason because the maximum rate of the homogeneous crystallization of PEN melts is observed in the vicinity of 215ЊC.The viscosity behavior of the PEN melt with crystalliza-tion in Fig.3may be accounted for by adopting the Mooney equation in a qualitative manner [19].ln h =h 1K E F 21ϪF 2=F m2W.J.Yoon et al./Polymer 41(2000)4933–49424938Fig.4.(continued )Table 1The values of T m H and T m HH of PEN with frequency (230,240and 250indicate temperature.(a)and (b)indicate v 0 a and v 0 b ;respectively (see Fig.6).1,3and 5indicate frequencyT m HT m HH T m HT m HH T m HT m HH PEN230(a)259.2272.1PEN240(a)266.7PEN250(a)270.1PEN230(b)264.1270.9PEN240(b)272.1PEN250(b)280.1PEN2301255.6270.3PEN2401259.3269.3PEN2501269.1PEN2303256.0270.0PEN2403261.9268.7PEN2503270.4PEN2305256.2269.7PEN2405263.6268.0PEN2505270.7F m true volume of fillerapparent volume occupied by the filler3 in which h is the viscosity of the suspension,h l is the viscosity of the suspending medium,f2is the volume frac-tion of thefiller,f m is the maximum volume fraction that thefiller can have,and K E is the Einstein coefficient,whose value is known to be2.5for the dispersed sphericalfiller.W.J.Yoon et al./Polymer41(2000)4933–49424939Fig.5.WAXD patterns of PEN isothermally crystallized at(A)230ЊC,(B)240ЊC and(C)250ЊC at various frequencies.Referring to the Mooney equation,the crystallization patterns of PEN melts at 230ЊC and at 250ЊC are distinc-tively different from each other.The Mooney equation predicts that the degree of increasing the suspension visc-osity with increasing f 2is greatly increased if the spheres form aggregates because the aggregation of spheres (spheru-litic crystallites or crystals in this study)increases the appar-ent filler volume fraction.That is,the immobile portions (homogeneous molten PEN matrix in this study)caged by aggregated spheres also act as filler portion.On this assump-tion,it may be suggested that an application of higher shear rate during isothermal crystallization tends to increase the heterogeneous crystallization characteristics.Hence,the higher nucleation density and higher growth rate of the nucleated crystallites is obtained at higher frequency,and the resultant is more abundant with less stable a -form crys-tals (this will be discussed later in detail).The melt endotherms of quiescently and shear-induced crystallized PEN were shown in Fig.4and the correspond-ing peak temperatures are listed in Table 1.The double melting endotherm behavior is displayed during heating the PEN sample in the DSC cell.In the melting process of the shear-induced crystallized PEN sample,three endother-mic peaks are identified;a broad endotherm,a low endotherm (T m H ),and a high endotherm (T m HH )as shown in Fig.4.The broad endotherm might be due to the thermal history during cooling and reheating,and both low and high endotherms are due to the melting of original lamella and recrystallized one,respectively.These results well coincide with the results of Zachman et al.[20]:(1)no change of crystal modification is observed during DSC scanning;(2)the double melting behavior of PEN is due to the mechan-ism based on melting and recrystallization;(3)the b -form crystal has the T m higher than the a -form crystal by 2ЊC;and (4)the peaks of two forms of crystal are not separated in DSC thermogramsIn Fig.4(A)–(C)v 0rad =s indicates quiescent crystal-lization.(A)indicates that the PEN sample was crystallized at 230,240,and 250ЊC for the same time that required in the ARES experiments,and (B)expresses the PEN sample crys-tallized in an oil bath at the same temperature as in (A)for the time long enough to fully crystallize.Since the crystal-lization time in (A)is much shorter than in (B),an exother-mic peak is observed in the thermogram (A)at around 205ЊC.The v 0rad =s (b)curves in Fig.4(B)show a single melting peak.The T m shifts to higher temperature and peak width gets narrower as the crystallization time and tempera-ture are increased.This is attributable to the increased perfectness of the resultant crystal structure,which is observed more clearly when the sample is crystallized at higher temperature as can be seen in Fig.4(C).Only the b -form crystal exists when the sample is isothermally crys-tallized at 250ЊC after having melted at 300ЊC.This result matches well with the X-ray data.As mentioned the T m of the b -form crystal is higher than the a -form crystal by 2–4ЊC.It has been known that PEN has two different triclinic crystal structures.Buchner et al.reported that crystalW.J.Yoon et al./Polymer 41(2000)4933–49424940Fig.5.(continued )structures are influenced by both melting and isothermal crystallization temperature.They observed that the b -form crystal appeared mainly when PEN was isothermally crys-tallized above 230ЊC quiescently and the a -form crystal did below 230ЊC after having melted at 300ЊC [20].Fig.5presents WAXD patterns of PEN specimens shear-inducedcrystallized at (A)230ЊC,(B)240ЊC,(C)250ЊC at several frequencies.In Fig.5(A)the WAXD patterns for v 0rad =s shows diffraction peaks at 15.6and 23.3Њwhich correspond to (010)and (100)plane of the a -form crystal,respectively.The intensity of these peaks has a tendency to increase with increasing frequency.It means that the appli-cation of shear promotes the formation of the a -form crystal and the increase of frequency increases the content of the a -form crystal.In Fig.5(B)the (010)plane peak of the a -form crystal is smaller than that of the sample crystallized at 230ЊC in Fig.5(A)for v 0rad =s :However,the plane peak is increased with increasing frequency.In the case of the (100)plane peak,a shoulder appears at v 0rad =s :As frequency increases,the intensity of the plane peak standing for the a -form crystal shows tendency to increase.Particu-larly,for v 0rad =s in Fig.5(C)any plane peak of the a -form crystal is not observed,which is consistent with the results reported by Buchner et al.[20].The (010)and (100)plane peaks appear simultaneously,and keep on growing with increasing frequency.In addition,all diffraction peaks of Fig.5shift to lower angle when frequency is increased.This suggests that there is deformation in the crystal struc-tures as well.Thus,this X-ray trace of the sample is similar to those of Fig.5(A)and (B),suggesting similarity in the crystallization behavior at 230–250ЊC.In general,the b -form crystal is thermodynamically more stable but more difficult to nucleate than the a -form crystal and the form of the crystal is largely determined by kinetic factors during crystallization such as the rate of nucleation and spherulite growth [21].In the case of the a -form crystal,one chain passes through the unit cell and the chains in the crystal are extended.In the case of the b -form crystal,however,four chains pass through the unit cell and the chains in the crystal are not completely extended.When the polymer is sheared,the number of crystallites increases with shear rate,representing faster nucleation.Wolkowicz [14]mentioned that the number of crystallites increased exponentially with time at all shear rates.Also,this can be confirmed in Fig.6,which indicates that nuclea-tion becomes increasingly profuse with increasing frequency until the crystalline structure formed is no longer distinguishable with a microscope [3,22].Hence,the content of the a -form crystal in the speci-men increases with frequency because the a -form crys-tal is apt to nucleate due to fast nucleation.Consequently,the resultant a -form crystal is thermody-namically less stable than the b -form crystal because of much reduced entropy by molecular orientation under high shear force.References[1]Hill MJ,Keller A.J Macromol Sci (Phys)1969;B3(1):153.[2]Andrews EH.J Polym Sci 1966;A-2(4):663.[3]Haas TW,Maxwell B.Polym Eng Sci 1969;9:226.W.J.Yoon et al./Polymer 41(2000)4933–49424941(B)(A)(C)Fig.6.Polarizing optical micrographs of PEN crystallized at 240ЊC (A)v 0;(B)v 1;and (C)v 5:[4]Pennings AJ,van der Mark JMAA,Booj HC.kolloid Z v Z Polym1970;236:99.[5]Mackley MR,Keller A.Polymer1973;14:16.[6]Peterlin A.Polym Eng Sci1976;16:126.[7]Kobayashi K,Nagasawa T.J Macromol Sci(Phys)1970;B4:331.[8]Lagasse RR,Maxwell B.Polym Eng Sci1976;16:189.[9]Titomanlio G,Brucato V.Plastics Processing Society,The TenthAnnual Meeting,Akron,OH,1965,p.93.[10]Ulrich RD,Price FP.J Appl Polym Sci1976;14:401.[11]Eder G,Janeschizt-Kriehl H,Liedauer S.Progr Polym Sci1989;15:629.[12]Liedauer S,et al.Int Polym Proc VIII1993;3:236–44.[13]Moitzi J,Skallcky P.Polymer1993;34:3168.[14]Wolkowicz MD.J Polym Sci:Polym Symp1978;63:365.[15]Sherwood CH,Price FP,Stein RS.J Polym Sci;Polym Symp1977;63:77.[16]Imai M,et al.Phys.Rev.1995;B52:12696.[17]Kim JG,Park HJ,Lee JW.Korean J Rheol1997;4:174.[18]Carreau PJ,De Kee DCR,Chhabra RP.Rheology of polymericsystems,New York:Hanser,1997.[19]Nielsen LE.Polymer rheology,New York:Marcel Dekker,1977.[20]Buchner S,Wiswe D,Zachman HG.Polymer1989;30:480.[21]Zachman HG,Wiswe D,Riekel C.Macromol Chem Suppl1985;12:175.[22]Kim SP,Kim SC.Polym Eng Sci1993;33:83.W.J.Yoon et al./Polymer41(2000)4933–4942 4942。

SD使用介绍及Elsevier期刊投稿常识

SD使用介绍及Elsevier期刊投稿常识



Elsevier Editorial System (EES),集在线投稿、评审和编辑功能于 一体的电子平台。 2002建立, 3.2million active end users per year 1900 journals use EES 100,000 new manuscripts received per month EES 支持: 作者在线投稿并追踪稿件状态 指派编辑 编辑部/编辑在线邀请审稿专家 审稿专家在线审稿 编辑部管理稿件信息 基于网络,无需安装,available 24/7 year around
Submit a paper
Review and give recommendation
REJECT Revise the paper
[Revision required]
Michael Derntl: Basics of Research Paper Writing and Publishing. http://www.pri.univie.ac.at/~derntl/papers/meth-se.pdf
ScienceDirect化学的学科分类

化学 – 分析化学 – 化学(综合) – 电化学 – 无机化学 – 有机化学 – 物理和理论化学 – 光谱学

化学工程 – 生物工程 – 催化 – 化学工程(综合) – 化学品健康与安全 – 胶体与表面化学 – 过滤与分离 – 流体运动和传递过程 – 工艺化学和技术
内容
1) Elsevier期刊投稿流程 2) EES投稿平台
1) Elsevier期刊投稿流程
Elsevier学术期刊出版流程
a. 寻找合适的期刊 b. 准备论文 c. 提交论文 d. 检查状态

my first article散文

my first article散文

my first article散文I still remember the day when I wrote my first article. It was a sunny afternoon, and I was sitting at my desk, pen in hand, staring at a blank piece of paper. I had always loved writing, but I had never actually written an article before. I was nervous and excited at the same time.I started by jotting down some ideas. I thought about the things that mattered to me, the experiences that had shaped me, and the ideas that I wanted to share with the world. As I wrote, the words seemed to flow effortlessly from my pen. I was surprised at how easily the ideas came to me, and how clearly I was able to express them.Before I knew it, an hour had passed, and I had a page full of handwritten notes. I read through them, feeling a sense of pride and accomplishment. Those were my thoughts, my words, my voice. It was a powerful feeling.Over the next few days, I typed up my article and edited it carefully. I revised it several times, making sure that every sentence was clear and every word was chosen with care. Finally, I was ready to publish my first article.I submitted it to a local newspaper, and a few weeks later, I received a letter in the mail. My article had been accepted, and it wasgoing to be published in the next issue. I was overjoyed. My dream of becoming a writer was finally coming true.Looking back on that experience, I realize that writing that first article was more than just a成就感. It was a journey of self-discovery. It taught me that I had something valuable to say, and that my voice mattered. It gave me the confidence to keep writing, to keep sharing my ideas with the world.I will always cherish that first article, and the memories of the process of creating it. It will always remind me of the power of words, and the importance of following your dreams.。

sdarticle2

sdarticle2

Computational noteElectronic dipole polarizabilities of polychlorinated dibenzofurans and semiempirical PM6level performanceAndrea Alparone,Vito Librando *Research Centre for Analysis,Monitoring and Minimization Methods of Environmental Risk,Department of Chemistry,University of Catania,viale A.Doria 8,Catania I-95125,ItalyPolychlorinated dibenzofurans (PCDFs)are widespread and per-sistent environmental contaminants [1].Electronic dipole polariz-abilities (a )of PCDFs were previously computed at the B3LYP level with cc-pVDZ,6-31G Ãand 6-31G ÃÃbasis sets in order to elucidate the effect of the substituent position on the congener specific tox-icity [2,3]and aqueous solubility [4].Recently,semiempirical PM6method [5]has been implemented in MOPAC 2007package [6],giving satisfactory estimates of molecular properties such as heats of formation [5]and electronic a values [7,8].This work is principally concerned on the validation of the PM6method in the determination of a values,focusing attention on DF and the 135PCDF congeners (Fig.S1of the Supporting Material).Static a ij (i,j =x ,y ,z )components were calculated at the AM1,PM3and PM6levels.Additionally,we computed a ij values for DF and its octacloro substituted congener at the HF,MP2and PBE0levels with aug-cc-pVDZ basis set on the B3LYP/6-31G ÃÃgeometry.Present computations were performed with MOPAC 2007[6]and PC GAMESS [9,10]programs.Calculated average polarizability,h a i ¼1=3ða xx þa yy þa zz Þ,and polarizability anisotropy,D a ¼f 1½ða xx Àa yy Þ2þða xx Àa zz Þ2þða yy Àa zz Þ2þ6ða 2xy þa 2xz þa 2yz Þ g 1=2,are given in Tables S1–S3of the Supporting Material.The results show that PM6is noticeably superior to both the commonly em-ployed semiempirical AM1and PM3methods,reproducing the PBE0/aug-cc-pVDZ (and also MP2/aug-cc-pVDZ)h a i values of DF and 1,2,3,4,5,6,7,8-OCDF within 5a.u.(2–3%)and D a data within 8–11a.u.(3–8%),geometrical effects (PM6vs.B3LYP/6-31G ÃÃ)being almost negligible.Note that the corresponding deviations for h a i obtained using the AM1,PM3and B3LYP/6-31G ÃÃ[3]data are substantially larger,being 36–94a.u.(25–34%),41–76a.u.(27–28%),24–47a.u.(16–17%),respectively,while those for D a are 22–25a.u.(9–20%),16–43a.u.(12–18%)and 11–14a.u.(4–11%),respectively.However,least-mean squared fitting linear relationships between the semiempirical and B3LYP/6-31G ÃÃh a i and D a data (See Figs.S2and S3of the Supporting Material)aresatisfactory (r 2=0.97–1.00).As can be appreciated from Figs.S4and S5of the Supporting Material,on passing from PM6to AM1(PM3),h a i and D a values decrease and increase by 21–33%(26–28%)and 13–31%(19–23%),respectively.These discrepancies are principally originated from differences in the out of the plane polarizability component.Due to its relatively low computational cost and good accuracy,PM6is a promising method for the predic-tion of a of large p -conjugated systems and is particularly indi-cated for QSPR studies.AcknowledgementWork partially supported by MIUR,Rome.Appendix A.Supplementary dataSupplementary data associated with this article can be found,in the online version,at doi:10.1016/j.theochem.2008.09.023.References[1]S.Safe,Crit.Rev.Toxicol.21(1990)51.[2]S.Hirokawa,T.Imasaka,T.Imasaka,Chem.Res.Toxicol.18(2005)232.[3]C.Gu,X.Jiang,X.Ju,G.Yu,Y.Bian,Chemosphere 67(2007)1325.[4]G.Yang,X.Zhang,Z.Wang,H.Liu,X.Ju,J.Mol.Struct.(Theochem)766(2006)25.[5]J.J.P.Stewart,J.Mol.Model.13(2007)1173.[6]J.J.P.Stewart,MOPAC 2007,Stewart Computational Chemistry,Colorado Springs,CO,USA,[7]T.Puzyn,N.Suzuki,M.Haranczyk,J.Rak,J.Chem.Inf.Model.48(2008)1174.[8]A.Alparone,V.Librando,Z.Minniti,Chem.Phys.Lett.460(2008)151.[9]M.W.Schmidt,K.K.Baldridge,J.A.Boatz,S.T.Elbert,M.S.Gordon,J.H.Jensen,S.Koseki,N.Matsunaga,K.A.Nguyen,S.J.Su,T.L.Windus,M.Dupuis,J.A.Montgomery,put.Chem.14(1993)1347.[10]A.A.Granovsky,PC GAMESS version 7.0,Available from:<http://classic.chem.msu.su/gran/gamess/index.html/>.0166-1280/$-see front matter Ó2008Elsevier B.V.All rights reserved.doi:10.1016/j.theochem.2008.09.023*Corresponding author.Tel.:+39957385201;fax:+3995580138.E-mail address:vlibrando@unict.it (V.Librando).Journal of Molecular Structure:THEOCHEM 894(2009)128Contents lists available at ScienceDirectJournal of Molecular Structure:THEOCHEMj o ur na l h o me pa ge :w w w.e ls e v ie r.c o m/lo c a t e/t he o c hem。

Elsevier(爱思唯尔)数据库在科技论文写作中的应用

Elsevier(爱思唯尔)数据库在科技论文写作中的应用

Elsevier(爱思唯尔)数据库在科技论文写作中的应用张成(石家庄经济学院,河北石家庄 050031)前言Elsevier(爱思唯尔)是一家世界领先的科学、技术和医学信息产品和服务提供商,其主要产品包括学术期刊、教科书和数据库。

爱思唯尔著名数据库ScienceDirect,简称SD,是著名的学术数据库,SD是Elsevier公司的核心产品。

石家庄经济学院已与中国地质图书馆达成了文献资源的共建共享协议,我校师生可以利用中国地质图书馆为我校提供的“中国地质图书馆远程访问系统”的VPN账号访问和利用爱思唯尔著名数据库ScienceDirect。

本文结合具体实例重点介绍ScienceDirect数据库在科技论文写作中的使用方法以及技巧。

1 Elsevier简介爱思唯尔(Elsevier)是世界上最大的医学与其他科学文献出版社之一,其前身可追溯自16世纪,而现代公司则起于1880年,其作者和审稿多由世界著名的诺贝尔奖获得者担任。

期刊有2200多种,包括《柳叶刀》和《细胞》等世界著名期刊;图书有4000多册/年,包括《格雷氏解剖学》等著名出版品牌的参考工具书;数据库有ScienceDirect、Scopus、Embase、xpharm等。

2 ScienceDirect数据库2.1 ScienceDirect数据库简介SD是Elsevier公司的核心产品,是全球最著名的科技医学全文数据库之一,其直观友好的使用界面,使研究人员可以迅速链接到Elsevier出版社丰富的电子资源,包括期刊全文、单行本电子书、参考工具书、手册以及图书系列等。

用户可在线访问24个学科2200多种期刊,15000多种图书,查看1000多万篇全文文献。

全球范围内,ScienceDirect获得了134个国家1100万科研人员的认可,每月全文下载量达数百万篇,目前,已有200多所高校、中科院、国家图书馆等机构加入SD中国集团。

2.2 网站登录双击“Inte rnet Explorer”,地址栏输入:/,进入“爱思唯尔”检索网站主页。

article英文作文格式

article英文作文格式

article英文作文格式1. I woke up late this morning, feeling groggy and disoriented. My alarm clock had failed me, leaving me scrambling to get ready for the day. I rushed through my morning routine, throwing on clothes and grabbing a quick breakfast. It was a chaotic start to the day, but I managed to make it out the door on time.2. As I walked to work, I noticed the sun shining brightly in the clear blue sky. The weather was perfect not too hot, not too cold. It put me in a good mood and made the walk more enjoyable. I couldn't help but smile as I passed by people on the street, feeling the warmth of the sun on my skin.3. When I arrived at the office, I was greeted by a mountain of paperwork on my desk. It seemed like there was no end to the tasks that needed to be completed. I took a deep breath and dove right in, determined to tackle each item one by one. The day was going to be busy, but I was upfor the challenge.4. During lunchtime, I decided to take a break and go for a walk outside. The fresh air and change of scenery helped clear my mind and recharge my energy. I strolled through the nearby park, admiring the colorful flowers and listening to the birds chirping. It was a peaceful moment amidst the chaos of the workday.5. Back at the office, I found myself in a meeting with my colleagues. We discussed upcoming projects and brainstormed ideas. It was a collaborative and productive session, with everyone sharing their thoughts and opinions.I enjoyed the lively discussion and felt inspired by the creativity in the room.6. As the workday came to a close, I felt a sense of accomplishment. Despite the challenges and busyness, I had managed to complete all my tasks. I packed up my things and headed home, looking forward to a relaxing evening.7. At home, I decided to unwind by watching a movie. Itwas a comedy that had me laughing out loud. The humor was a welcome distraction from the stresses of the day. I curled up on the couch with a bowl of popcorn, enjoying the movie and letting the laughter wash over me.8. Finally, it was time to go to bed. I crawled under the covers, feeling grateful for the day that had passed. It had been a rollercoaster of emotions, but ultimately a fulfilling and rewarding experience. As I closed my eyes, I looked forward to what tomorrow would bring.。

第三章期刊文献数据库检索第六节Elsevier电子期刊数据库

第三章期刊文献数据库检索第六节Elsevier电子期刊数据库
3.精确检索:检索词加上引号“”表示短语精确检 索,系统查找与引号内完全匹配的记录。
4.作者检索 先输入名的全称或缩写,然后输入姓的全拼
5.截词符 * 表示无限截词,即在检索词的末尾加上*,表示
可以代替n个字母。 6.禁用词(stop word)
系统遇到禁用词,会自动省略,以空格取代。 主要的禁用词有of、the、in、she、he、to be、 because、if、when等。
7.系统具有识别单复数的功能,输入单词的单数形 式,可以检索到该单词的单数、复数及所有格形 式。不规则复数变化除外。
8.检索希腊字母时,用其英文拼写代替。 9.上下标字符按普通字符输入。
四、检索结果显示与全文下载
(一)通过浏览检索,得到期刊列表。找到 所需期刊,点击期刊名,就可进入期刊的 卷期/目次页面浏览。
一、概况 二、检索途径 三、检索规则 四、检索结果显示与全文下载 五、个性化服务
一、概况
Elsevier公司出版的电子期刊数据库 ScienceDirect(SD)是的公司核心电子产品 之一。该数据库目前已经收录了自1995年以 来的2500多种电子期刊上的全文,共800多 万篇,至今下载量达38亿,内容学科包括4 大类24个学科。
(二)通过快速检索、高级检索、专家检索 可以得到文章记录列表。记录可以按出版 时间索功能、检索界面优化, 还提供了使用者多角度、多层次的个性化 服务,如保存检索式、察看检索历史、各 类快速链接,定制文献通报服务等。
个性化服务内容
(1)查看近期检索操作,可以保存检索式、 检索结果等。
(2)定制个人喜爱的期刊及目次(Favorites) (3)定制文献通报服务(E-mail Alert) (4)建立快速链接(My Quick Links) (5)上面提到的通报服务,用户还可以利用

SD数据库使用说明(教学课件)

SD数据库使用说明(教学课件)

AND OR AND NOT
默认算符,要求多个检索词同时出现在文章中 检索词中的任意一个或多个出现在文章中 后面所跟的词不出现在文章中
通配符 * 取代单词中的任意个(0,1,2…)字母
通配符 ? 取代单词中的1个字母
W/n PRE/n “” ‘’
() 作者检索
两词相隔不超过n个词,词序不定 两词相隔不超过n个词,词序一定 宽松短语检索,标点符号、连字符、停用字等会被自动忽略
检索-Search:检索历史
检索-Search:检索保存与检索提示
检索-Search:发送文章与引文输出
E-mail文章、输出引文
检索-Search:发送文章与引文输出
检索-Search:排序与二次检索
二次检索 title(therapy) 按时间或相关度排序
检索-Search:查看文章与引文提示
字段全称
简写编码
all
all
title-abs-key
tak
title
ttl
abstract
abs
keywords
key
authors
aut
specific-author
aus
references
ref
srctitle
src
affiliation
aff
专家检索模式: Field_name (search_term)
Elsevier 是Reed Elsevier集团中的科学部门, 全球最 大的科学文献出版发行商.
Elsevier 的理念:通过提供信息的解决方案,提高全球 范围内研究人员的效率,推动科学,技术和医学的发展.
数据库产品:因您而变 大势所趋
Elsevier的作者:诺贝尔奖得主

spm英文作文格式article

spm英文作文格式article

spm英文作文格式article下载温馨提示:该文档是我店铺精心编制而成,希望大家下载以后,能够帮助大家解决实际的问题。

文档下载后可定制随意修改,请根据实际需要进行相应的调整和使用,谢谢!并且,本店铺为大家提供各种各样类型的实用资料,如教育随笔、日记赏析、句子摘抄、古诗大全、经典美文、话题作文、工作总结、词语解析、文案摘录、其他资料等等,如想了解不同资料格式和写法,敬请关注!Download tips: This document is carefully compiled by theeditor. I hope that after you download them,they can help yousolve practical problems. The document can be customized andmodified after downloading,please adjust and use it according toactual needs, thank you!In addition, our shop provides you with various types ofpractical materials,such as educational essays, diaryappreciation,sentence excerpts,ancient poems,classic articles,topic composition,work summary,word parsing,copyexcerpts,other materials and so on,want to know different data formats andwriting methods,please pay attention!I love music. It makes me feel happy and relaxed.Yesterday I went to the park. It was a sunny day. There were many people there.My dog is so cute. He always follows me around.I had a great meal today. The food was delicious.I don't like rainy days. They make me feel down.。

英文作文article格式

英文作文article格式

英文作文article格式Title: The Power of Music。

Music is a universal language that has the ability to transcend cultural barriers and connect people from all walks of life. It has the power to evoke emotions, bring back memories, and even inspire change. Whether it's the soothing melodies of a lullaby or the energetic beats of a rock concert, music has the ability to touch our souls and leave a lasting impact.In today's fast-paced world, music serves as a form of escapism for many. It provides a temporary refuge from the stresses and pressures of everyday life. With just a few notes, a song can transport us to a different time and place, allowing us to momentarily forget our worries and immerse ourselves in the rhythm and melody. It is a form of therapy that can heal our souls and rejuvenate our spirits.Furthermore, music has the power to unite people in away that few other things can. It brings together individuals from different backgrounds and cultures, creating a sense of community and belonging. Whether it's through a shared love for a particular genre or acollective experience at a concert, music has the ability to break down barriers and foster a sense of togetherness. It is a language that everyone can understand, regardless of their native tongue.Moreover, music has the ability to evoke strong emotions and memories. A single song can transport us back in time, evoking memories of past experiences and emotions. It has the power to make us laugh, cry, or feel a sense of nostalgia. It has the ability to capture the essence of a moment and preserve it forever in our hearts and minds.In addition, music has the power to inspire change and bring about social awareness. Throughout history, musicians have used their platform to raise awareness about important social issues and advocate for change. From Bob Dylan's protest songs to Beyoncé's empowering anthems, music has the ability to spark conversations and ignite movements. Ithas the power to give a voice to the voiceless and inspire individuals to take action.In conclusion, music is a powerful force that has the ability to transcend boundaries and connect people on a deeper level. It serves as a form of therapy, a means of unity, a source of emotional connection, and a catalyst for change. Whether we're singing in the shower or attending a live concert, music has the power to touch our souls and leave a lasting impact. So, let's embrace the power of music and let it guide us on our journey through life.。

羰基保护_sdarticle

羰基保护_sdarticle

Copper(II)tetrafluoroborate as a novel and highly efficientcatalyst for acetal formationRaj Kumar and Asit K.Chakraborti *Department of Medicinal Chemistry,National Institute of Pharmaceutical Education and Research (NIPER),S ector 67,S .A.S .Nagar,Punjab 160062,IndiaReceived 24July 2005;revised 23September 2005;accepted 28September 2005Available online 11October 2005Dedicated to Professor Mark S.CushmanAbstract—Commercially available copper(II)tetrafluoroborate hydrate has been found to be a highly efficient catalyst for dimethyl/diethyl acetal formation in high yields from aldehydes and ketones by reaction with trimethyl/triethyl orthoformate at room tem-perature and in short period.Acetalisation was carried out under solvent-free conditions with electrophilic aldehydes/ketones.For weakly electrophilic aldehydes/ketones (e.g.,benzaldehyde,cinnamaldehyde and acetophenone)and for aldehydes having a substi-tuent that can coordinate with the catalyst,the corresponding alcohol was used as solvent.Ó2005Elsevier Ltd.All rights reserved.1.IntroductionProtection of aldehyde and ketone carbonyl groups is a frequently desired exercise in organic synthesis as it is often necessary to carry out a reaction on a multifunc-tional substrate without affecting an aldehyde/ketone group.One convenient method of protecting aldehydes and ketones is to convert them into the corresponding acetals.1Acetalisation can be achieved by treatment with alcohols in the presence of a protic 1,2or Lewis 1,3acid catalyst.A common regimen for acetal formation is protic 1,4or Lewis 1,5acid catalysed reaction of alde-hydes and ketones with trialkyl orthoformates.Other methods use MeOH–PhSO 2NHOH–MeONa,1b alkoxy-silanes in the presence of TMSOTf,1b (EtO)3CH–DDQ–EtOH 6and CAN–Na 2CO 3–ROH.7However,these methods have one or more drawbacks such as long reaction times,high temperatures,use of costly re-agents/catalysts,use of additional reagents,requirement of special efforts for catalyst preparation,requirement of stoichiometric amount of the catalysts,the need to use special apparatus and moderate yields and side reac-tions.Thus,the development of an improved method is still desirable.2.Results and discussionsWhen designing a new method,we realised that the use of trialkyl orthoformates as the acetalisation agent in the presence of a suitable transition metal catalyst should constitute a better procedure operable under mild conditions.The efficiency of the method would depend upon the coordination property of the metal catalyst to activate trialkyl orthoformate and/or the carbonyl substrate.Recently,we have reported that copper(II)tetrafluoroborate is an excellent catalyst for electrophilic activation during acylation,8diacetate for-mation 9and thia-Michael addition 10reactions.In this report,we disclose a highly efficient acetal formation reaction catalysed by copper(II)tetrafluoroborate (Scheme 1).Various aldehydes and ketones were treated with tri-methyl orthoformate in the presence of Cu(BF 4)2Æx H 2O0040-4039/$-see front matter Ó2005Elsevier Ltd.All rights reserved.doi:10.1016/j.tetlet.2005.09.168Keywords :Dimethyl acetals;Diethyl acetals;Aldehydes;Ketones;Copper(II)tetrafluoroborate hydrate;Catalyst;Trimethyl orthofor-mate;Triethyl orthoformate.*Corresponding author.Tel.:+9101722214682686;fax:+9101722214692;e-mail:akchakraborti@niper.ac.in(1mol %)at $25–30°C under neat conditions.The reactions were monitored by IR and GCMS and the optimum results are provided in Table 1.Substituted benzaldehydes with Me,Cl,Br,NO 2and OCOPh groups (entries 1–7),1-naphthaldehyde (entry 8),9-anthraldehyde (entry 9),aryl alkyl aldehydes (entries 10and 11)and saturated cyclic ketones (entries 12and 13)afforded excellent results after 2–15min.The reac-tions could also be monitored visually:immediately after the addition of the catalyst to the mixture of alde-hyde and trimethyl orthoformate an exothermic reaction takes place and the reaction mixture becomes homoge-neous (for solid aldehydes)indicating completion of ace-tal formation.In the case of 9-anthraldehyde,as the product was solid,a small excess (3equiv)of trimethyl orthoformate was required.In the cases of benzaldehyde,cinnamaldehyde,aceto-phenone and aldehydes bearing substituents that are capable of coordinating with the metal ion,the acetalformation was slow under neat conditions.However,in these cases,the reactions proceeded well using MeOH as solvent affording excellent yields (Table 2).The phenyl/styryl groups in benzaldehyde,cinnamalde-hyde and acetophenone made aldehyde/ketone carbonyl less electrophilic due to resonance and inhibited the effective formation of coordinate bonds with the cata-lyst.For aldehydes bearing substituents that can coordi-nate with the metal cation (e.g.,OR,F,CN,NMe 2,etc.)no effective activation of trimethyl orthoformate by the metal salt took place and acetal formation was retarded.The moderate yield obtained with 4-dimethylamino-benzaldehyde after 12h (Table 2,entry 6)supported the role of a coordinating effect of the substituent in influencing acetal parison of acetal for-mation from 4-methylbenzaldehyde,4-chlorobenzalde-hyde and 4-nitrobenzaldehyde (Table 1,entries 1–3)with those from 4-methoxybenzaldehyde,4-fluorobenz-aldehyde and 4-cyanobenzaldehyde (Table 2,entries 2–4),respectively,highlighted the coordinating effect of the substituents in the latter cases.The role of MeOH may be explained by the fact that initial reaction ofTable 2.Cu(BF 4)2Æx H 2O catalysed dimethyl acetal formation from aldehydes/ketones in dry MeOH aEntryAldehyde/ketone Time (min)Yield (%)b ,cCHO1R =H 593d 2R =F 10953R =CN 10924R =OMe 20915R =NMe 212h58CHOO R6R =Me 30887R =c -C 5H 910928CHOPh20919O308510S 2082O111.5h 96aThe aldehyde/ketone (2.5mmol)in dry methanol (1mL)was treated with CH(OMe)3(2.0equiv)in the presence of Cu(BF 4)2Æx H 2O (1mol %)at room temperature ($25–30°C).bIsolated yield of the corresponding acetal.cThe products were characterised by IR and NMR.dA 36%yield was obtained on carrying out the reaction under neat conditions.Table 1.Cu(BF 4)2Æx H 2O catalysed dimethyl acetal formation from aldehydes/ketones under solvent-free conditions aEntryAldehyde/ketone Time (min)Yield (%)b ,cCHO3R 1R 21R 1=R 2=H;R 3=Me 5922R 1=R 2=H;R 3=Cl 5903R 1=R 2=H;R 3=NO 23924R 1=R 2=H;R 3=OCOPh 5915R 1=Br;R 2=R 3=H 5886R 1=Cl;R 2=R 3=H 5907R 1=R 3=H;R 2=NO 28928CHO15859CHO1582d10Ph CHO 28511CHOPh38612O57813O295aThe aldehyde/ketone (2.5mmol)was treated with CH(OMe)3(2.0equiv)in the presence of Cu(BF 4)2Æx H 2O (1mol %)at room temperature ($25–30°C)under neat conditions.bIsolated yield of the corresponding acetal.cThe products were characterised by IR,NMR.dThe reaction was carried out using 3equiv of CH (OMe)3.8320R.Kumar,A.K.Chakraborti /Tetrahedron Letters 46(2005)8319–8323aldehyde with MeOH leads to the formation of a hemi-acetal,which undergoes nucleophilic attack on trimethyl orthoformate complexed with Cu(BF 4)2Æx H 2O and results in acetal formation.4Since there are limited reports for diethyl acetal forma-tion,3e,f,4,5c–e,gwe planned to evaluate the catalytic effi-ciency of Cu(BF 4)2Æx H 2O during the reaction of a few representative aldehydes and ketones with triethyl orthoformate (Table 3).Excellent results were obtained in each case.As observed in the case of dimethyl acetal formation,the reactions of benzaldehyde,cinnamaldehyde and aceto-phenone required dry EtOH as solvent for diethyl acetal formation.A comparison of the results of entries 1and 6(Table 2)prompted us to study selective acetal formation during intermolecular competition between benzaldehyde 1and 4-dimethylaminobenzaldehyde 2.Thus,a mixture of 1(2.5mmol)and 2(2.5mmol)in dry MeOH (1mL)was treated with trimethyl orthoformate (5mmol)in the presence of Cu(BF 4)2Æx H 2O (1mol %)for 5min at room temperature (Scheme 2).Excellent selectivity was observed,(dimethoxymethyl)benzene 3and 4-(dimethoxymethyl)-N ,N -dimethylaniline 4were formed in a ratio of 88:12(NMR).Similarly,the differ-ence in the rate of reaction of 1and acetophenone 5(Table 2,compare the results of entries 1and 11)encouraged us to study the selectivity of acetal forma-tion during inter-and intramolecular competition stud-ies involving aldehyde and ketone carbonyl groups.Thereaction of 1(2.5mmol)and 5(2.5mmol)with trimethyl orthoformate (5mmol)in dry MeOH (1mL)in the pres-ence of Cu(BF 4)2Æx H 2O (1mol %)at room temperature for 5min (Scheme 2)resulted in the formation of 3and 2,2-dimethoxy-1-phenylethane 6in a ratio of 86:14(NMR).The reaction of 4-acetylbenzaldehyde 7(2.5mmol)with trimethyl orthoformate (5mmol)in MeOH (1mL)in the presence of Cu(BF 4)2Æx H 2O (1mol %)for 5min at room temperature resulted in the formation of 4-(dimethoxymethyl)acetophenone 8and 2,2-dimethoxy-(40-dimethoxymethyl)-1-phenyl-ethane 9in a ratio of 77:23(GCMS).3.ConclusionsWe have described herein the use of Cu(BF 4)2Æx H 2O as ahighly efficient and reusable catalyst for dimethyl and diethyl acetal formation at room temperature.The advantages include,(i)the use of a cheap,easy to handle and commercially available catalyst,(ii)room tempera-ture reaction conditions,(iii)short reaction times,(iv)high yields and (v)excellent chemoselectivity.4.Experimental4.1.Typical procedure for acetal formation under neat conditionsTo a magnetically stirred mixture of 4-methylbenzalde-hyde (0.3g, 2.5mmol)and trimethyl orthoformate (0.53g,5mmol),Cu(BF 4)2Æx H 2O (6.0mg,0.025mmol,1mol %)was added and the mixture was stirred at 25–30°C until completion of the reaction (5min,TLC,IR).The mixture was diluted with saturated aq NaHCO 3(10mL)and extracted with EtOAc (3·10mL).TheTable 3.Cu(BF 4)2Æx H 2O catalysed diethyl acetal formation from aldehydes and ketones aEntryAldehyde/ketone Time (min)Yield (%)b ,cCHO1R =H 1093d 2R =Me 3953R =NO 25954CHO Ph 10925CHOPh 380d6O375The aldehyde/ketone (1equiv)was treated with CH(OEt)3(2.0equiv)in the presence of Cu(BF 4)2Æx H 2O (1mol %)at rt ($25–30°C)in the absence of solvent (except for entries 1,5and 7).bIsolated yield of the corresponding acetal.cThe products were characterised by IR,NMR.dThe reaction was carried out in dry ethanol (1mL).R.Kumar,A.K.Chakraborti /Tetrahedron Letters 46(2005)8319–83238321combined EtOAc extracts were washed with water(2·10mL),dried(Na2SO4)and concentrated under reduced pressure to afford4-(dimethoxy)methylbenzene(colour-less oil,0.415g,92%,entry1,Table1),IR(neat):2936, 2828,1618,1447,1353,1201,1105,1054,912, 807cmÀ1;1H NMR(300MHz,CDCl3):d=2.33(s, 3H),3.30(s,6H),5.35(s,1H),7.15(d,2H,J=7.6Hz), 7.32(d,2H,J=7.6Hz);13C NMR(75MHz,CDCl3): d=21.2,52.53,103.16,126.56,128.81,135.13,138.06, identical with an authentic sample.5e5.Representative experimental procedure for acetalformation in the presence of solventTo a magnetically stirred mixture of4-cyanobenzalde-hyde(0.327g, 2.5mmol)and trimethyl orthoformate (0.53g,5mmol)in dry MeOH(1mL),Cu(BF4)2Æx H2O (6.0mg,0.025mmol,1mol%)was added and the mix-ture was stirred at25–30°C until completion of the reac-tion(10min,TLC,IR).The reaction mixture was diluted with saturated aq NaHCO3(10mL)and extracted with EtOAc(3·10mL).The combined EtOAc extracts were washed with water(2·10mL), dried(Na2SO4)and concentrated under reduced pres-sure to afford pure4-(cyano)dimethoxymethylbenzene (colourless oil,0.407g,92%,entry3,Table2),IR(neat): 2938,2832,2229,1353,1209,1101,1057,988,822, 556cmÀ1;1H NMR(300MHz,CDCl3):d=3.32(s, 6H),5.43(s,1H),7.50(d,2H,J=8.3H z),7.68(d, 2H,J=8.3H z);13C NMR(75MHz,CDCl3): d=52.56,101.62,112.14,118.52,127.45,131.91, 143.10,identical with an authentic sample.2cThe remaining reactions were carried out following these general procedures.On each occasion,the spectral data(IR,1H NMR and13C NMR)of the prepared known compounds were found to be identical with those reported in the literature.The following compounds had not been reported.2-(Bromo)dimethoxymethylbenzene(Table1,entry5): IR(neat):2933,2829,1468,1364,1204,1103,1057, 980,755cmÀ1.1H NMR(300MHz,CDCl3):d=3.35 (s,6H),5.55(s,1H),7.14(t,1H,J=7.5Hz),7.28(t, 1H,J=7.5Hz),7.52(d,1H,J=7.6Hz),7.59(d,1H, J=7.6Hz).13C NMR(75MHz,CDCl3):d=53.57, 102.71,122.75,126.92,128.18,129.84,132.66,136.68. Anal.Calcd for C9H11BrO2:C,46.78;H,4.80.Found. C,46.80;H, 4.82.2-(Chloro)dimethoxymethylbenzene (Table1,entry6):IR(neat):2934,2830,1366,1201, 1107,1058,981,756cmÀ1.1H NMR(300MHz, CDCl3):d=3.37(s,6H),5.62(s,1H),7.22–7.29(m, 2H),7.33–7.36(m,1H),7.60–7.63(m,1H).13C NMR (75MHz,CDCl3):d=53.68,100.86,126.45,128.02, 129.50,129.65,133.11,135.28.Anal.Calcd for C9H11ClO2:C,57.92;H, 5.94.Found.C,57.91;H, 5.97.9-Dimethoxymethylanthracene(Table1,entry9): Mp:107–108°C IR(KBr):2932,1448,1186,1105, 1066,891,740cmÀ1.1H NMR(300MHz,CDCl3): d=3.50(s,6H),6.53(s,1H),7.38–7.61(m,4H),7.93 (d,2H,J=8.4Hz),8.39(s,1H),8.68(d,2H, J=8.4Hz).13C NMR(75MHz,CDCl3):d=53.68,100.86,126.45,128.02,129.50,129.65,133.11,135.28. Anal.Calcd for C17H16O2:C,80.93;H,6.39.Found. C,80.96;H,6.41.3,4-(Dimethoxy)dimethoxymethylbenz-ene(Table2,entry6):IR(neat):2937,2832,1607, 1594,1414,1259,1194,1136,1102,990,863,863,795, 762cmÀ1.1H NMR(300MHz,CDCl3):d=3.32(s, 6H),3.88(s,3H),3.90(s,3H),5.33(s,1H),6.84–6.97 (m,1H), 6.98–6.99(m,2H).13C NMR(75MHz, CDCl3):d=52.34,55.53,102.86,109.33,110.40, 119.00,126.48,130.61,148.64.Anal.Calcd for C11H16O4C,62.25;H,7.60.Found.C,62.23;H,7.63. 4-Cyclopentyloxy-3-methoxy dimethoxymethylbenzene (Table2,entry7):IR(neat):2954,2829,1607,1510, 1351,1264,1160,1102,1053,988,862,804cmÀ1.1H NMR(300MHz,CDCl3):d=1.57–1.61(m,2H), 1.79–1.97(m,6H),3.32(s,6H),3.85(s,3H),4.73–4.79 (m,1H),5.31(s,1H),6.84(d,1H,J=8.1Hz),6.93–6.97(m,2H).13C NMR(75MHz,CDCl3):d=24.03, 32.77,52.75,55.95,80.32,103.29,110.10,114.16, 119.07,130.54,147.73,149.81.Anal.Calcd for C15H22O4:C,67.64;H,8.33.Found.C,67.63;H,8.35.Supplementary dataSupplementary data associated with this article can be found,in the online version,at doi:10.1016/j.tetlet. 2005.09.168.References and notes1.(a)Meskens,F.A.J.Synthesis1981,501–521;(b)Greene,T.W.;Wuts,P.G.M.In Protecting Groups in Organic Synthesis,3rd ed.;John Wiley and Sons:New York,1999.2.p TsOH-MgSO4:(a)Lu,T.-J.;Yang,J.-F.;Sheu,L.-J.J.Org.Chem.1995,60,2931–2934;p TsOH under microwave heating:(b)Pe´rio, B.;Dozias,M.-J.;Jacquault,P.;Hamelin,J.Tetrahedron Lett.1997,38,7867–7870;Polymer-supported acid catalysts in an electroosmotic flow reactor:(c)Wiles, C.;Watts,P.;Haswell,S.J.Tetrahedron2005,61,5209–5217.3.Montmorillonite K-10:(a)Li,T.-S.;Li,S.-H.;Li,J.-T.;Li,H.-Z.J.Chem.Res.(S)1997,26–27;I2under microwaveheating:(b)Kalita, D.J.;Borah,R.;Sarma,J. C.Tetrahedron Lett.1998,39,4573–4574;MCM-41:(c) Tanaka,Y.;Sawamura,N.;Iwamoto,M.Tetrahedron Lett.1998,39,9457–9460;I2:(d)Basu,M.K.;Samajdar, S.;Becker,F.F.;Banik,B.K.Synlett2002,319–321;CoCl2:(e)Velusamy,S.;Punniyamurthy,T.Tetrahedron Lett.2004,45,4917–4920;RuCl3:(f)De,S.K.;Gibbs, R.A.Tetrahedron Lett.2004,45,8141–8144.4.TBATB:Gopinath,R.;Haque,S.J.;Patel,.Chem.2002,67,5842–5845.5.Rh(II)triphos:(a)Ott,J.;Tombo,G.M.R.;Schmid,B.;Venanzi,L.M.;Wang,G.;Ward,T.R.Tetrahedron Lett.1989,30,6151–6154;TiCl4:(b)Clerici,A.;Pastori,N.;Porta,O.Tetrahedron1998,54,15679–15690;ZrCl4:(c) Firouzabadi,H.;Iranpoor,N.;Karimi,B.Synlett1999, 321–323;NBS:(d)Karimi,B.;Seradj,H.;Ebrahimian,G.-R.Synlett1999,1456–1458;Bi(OTf)3:(e)Leonard,N.M.;Oswald,M.C.;Freiberg,D.A.;Nattier,B.A.;Smith,R.C.;Mohan,.Chem.2002,67,5202–5207;B10H14:(f)Lee,S.H.;Lee,J.H.;Yoon,C.M.Tetrahedron Lett.2002,43,2699–2703;LiBF4:(g)Hamada,N.;Kazahaya,K.;Shimizu,H.;Sato,T.Synlett2004,1074–8322R.Kumar,A.K.Chakraborti/Tetrahedron Letters46(2005)8319–83231076;InCl3:(h)Ranu,B.C.;Jana,R.;Samanta,S.Adv.S ynth.Catal.2004,346,446–450.6.Karimi, B.;Ashtiani, A.M.Chem.Lett.1999,1199–1200.7.Nair,V.;Rajan,R.;Balagopal,L.;Nair,L.G.;Ros,S.;Mohanan,K.Indian J.Chem.2005,44B,141–143.8.Chakraborti,A.K.;Gulhane,R.;Shivani Synthesis2004,111–115.9.Chakraborti,A.K.;Thilagavathi,R.;Kumar,R.Synthe-sis2004,831–833.10.Garg,S.K.;Kumar,R.;Chakraborti,A.K.TetrahedronLett.2005,46,1721–1724.R.Kumar,A.K.Chakraborti/Tetrahedron Letters46(2005)8319–83238323。

典型外文数据库SD和EI

典型外文数据库SD和EI

11.1 Science Direct 及时了解所在领域的最新研究?
检索提示
主题提示
期刊提示
引文提示
11.1 Science Direct How to publish with Elsevier?
•如何给Elsevier期刊投稿
•提高稿件接受率的技巧
在线投稿-SD主页 刊
11.1 Science Direct 选择期
Techstreet标准、Scirus、USPTO专利、esp@cenet等 多种数据库,是目前全球最全面的工程领域二次文献数据 库,并配有自由词库、分类码库、Ei受控词库等。 • Ei公司自1992年收录中国期刊,2003年被收录的在中国出
版的期刊已近300种。
11.2 Engineering Village 2
• 检索界面、途径与规则
• 辅助检索:索引、词表
• 快速检索(Quick Search)及实例 • 专家检索(Expert Search)及实例 • 精炼检索(Refine Search)及实例 • 组合检索(Combile Search)及实例 • 其它服务
快速检索
用户从一个下拉式菜单中选择要检索的各个项
Browse 浏览功能帮助看到以查询词开头的 依字母顺序排的主题词表。
11.2 Engineering Thesaurus search“Exact Term”检索 Village 2
Exact Term查询功能会为用户提供查询词在 控制词汇表中的按字母顺序排列的广义词、 狭义词和相关词
11.2 Engineering Village 2 EV2中的Compendex的使用方法
快速检索
限定条件
11.2 Engineering Village 2

山东大学硕士学位论文格式规范

山东大学硕士学位论文格式规范

山东大学2012年硕士学位论文格式规范1.1基本要求及结构硕士学位论文一般应用中文撰写,英语水平较好的同学提倡并鼓励用中、外文双语撰写。

学位论文字数一般为2-5万字左右(论文正文应该在40~80页),用A4纸张双面打印装订。

硕士学位论文一般应由以下几部分组成,依次为:1、论文封面;2、扉页;3、原创性声明和关于论文使用授权的声明(附件一);4、中、外文论文目录;5、中文摘要;6、英文摘要;7、符号说明;8、论文正文(包括文献综述);9、附录、附图表;10、引文出处及参考文献;11、致谢;12、攻读学位期间发表的学术论文目录;13、学位论文评阅及答辩情况(附件二);14、外文论文(软件工程硕士根据自己外文情况选择是否用外文撰写)。

1.2格式规范及撰写指南论文封面,由山东大学研究生院统一印制,学生个人不需要自己准备。

封面需填写的内容说明如下:(1)分类号:须采用《中国图书资料分类法》进行标注,软件工程专业为TP311;(2)单位代码:10422;(3)密级:非涉密(公开)论文及涉密论文的正本不需标注密级。

被确定为涉密论文的副本必须在封面右上角处注明所确定的论文密级(内部、或秘密或机密),同时还应注明相应的保密年限。

各密级的最长保密年限及书写格式规定如下:内部 5 年(最长5年,可少于5年);秘密★ 10 年(最长10年,可少于10年);机密★ 20 年(最长20年,可少于20年);(4)学号:填写自己的学号;(5)作者姓名:请填写个人姓名;(6)专业:以国务院学位委员会批准的专业目录中的专业为准,一般为二级学科,软件工程学科专业为软件工程硕士;(7)指导教师和技术职务:指导教师的署名技术职务一律以批准招生的为准,且只能写一名指导教师,实行双导师制,企业指导教师(限一名)必须写在括号中;(8)论文完成时间:上半年毕业答辩的同学填写4月10-20日中的某一日,下半年申请毕业答辩的同学填写10月10-20日中的某一日;以上几项字体须用四号加重黑体字打印。

igcse英语article范文

igcse英语article范文

igcse英语article范文The IGCSE English examination is a challenging yet rewarding experience for students seeking to demonstrate their proficiency in the English language. As an international qualification recognized globally, the IGCSE English exam assesses a range of essential skills, including reading comprehension, writing, and language use. Preparing for this examination requires a comprehensive understanding of the assessment criteria and a dedication to honing one's abilities in various aspects of the English language.One of the key components of the IGCSE English exam is the article writing task. This genre of writing is designed to test a student's ability to effectively communicate ideas, express opinions, and engage the reader. The article format allows students to showcase their creativity, organizational skills, and command of the English language.When approaching the article writing task, it is essential to understand the specific requirements and expectations outlined by the exam board. The IGCSE English syllabus typically specifies thelength, format, and content guidelines for the article. Students must be mindful of these parameters and ensure that their writing adheres to the prescribed structure.The opening paragraph of the article is crucial in capturing the reader's attention and setting the tone for the entire piece. It should introduce the central theme or focus of the article, providing a clear and concise overview of the main ideas to be explored. Effective use of hooks, such as thought-provoking questions or intriguing statements, can help draw the reader in and encourage them to continue reading.Following the introduction, the body paragraphs of the article should delve deeper into the chosen topic, presenting a logical and well-structured argument or discussion. Each paragraph should have a clear topic sentence that guides the reader through the progression of ideas. The use of supporting evidence, examples, and relevant facts can strengthen the overall persuasiveness and credibility of the article.Effective article writing also requires a strong command of language and a keen eye for detail. Students should strive to use a diverse vocabulary, employ various sentence structures, and maintain a cohesive and coherent flow throughout the piece. Attention to grammar, spelling, and punctuation is essential to ensure the articleis polished and professional in its presentation.One of the hallmarks of a well-written IGCSE English article is the ability to present a balanced and objective perspective on the chosen topic. While students are encouraged to express their own opinions and viewpoints, they should also acknowledge and address alternative perspectives or counterarguments. This demonstrates a nuanced understanding of the subject matter and a willingness to engage in critical thinking.In addition to the content and language proficiency, the IGCSE English article writing task also requires students to consider the intended audience and the appropriate tone and style for the piece. The article should be tailored to the specific needs and expectations of the reader, whether it be a general public audience or a more specialized readership.Effective article writing also involves the skillful use of organizational techniques, such as the incorporation of headings, subheadings, and transitional phrases. These elements help to guide the reader through the article, ensuring a clear and logical flow of ideas. Additionally, the use of relevant and engaging visuals, such as images or infographics, can enhance the overall presentation and appeal of the article.Throughout the writing process, students should engage in a cycle of drafting, revising, and editing to refine their work. This iterative approach allows for the identification and correction of any errors or weaknesses, as well as the opportunity to enhance the overall quality and coherence of the article.Ultimately, the IGCSE English article writing task is a valuable opportunity for students to showcase their language proficiency, critical thinking skills, and ability to communicate effectively in written form. By understanding the expectations of the exam and dedicating time to honing their writing abilities, students can approach this component of the IGCSE English examination with confidence and a strong foundation for success.。

  1. 1、下载文档前请自行甄别文档内容的完整性,平台不提供额外的编辑、内容补充、找答案等附加服务。
  2. 2、"仅部分预览"的文档,不可在线预览部分如存在完整性等问题,可反馈申请退款(可完整预览的文档不适用该条件!)。
  3. 3、如文档侵犯您的权益,请联系客服反馈,我们会尽快为您处理(人工客服工作时间:9:00-18:30)。

An approach to the simulation of PCMsin building applications using TRNSYSManuel Iba ´n ˜eza,1,Ana La ´zaro b ,Bele ´n Zalba b,2,Luisa F.Cabeza c,*a Dept.de Medi Ambient i Cie`ncies del So `l,Universitat de Lleida,Rovira Roure 191,25198Lleida,Spain b Dept.de Ingenierı´a Meca ´nica,Universidad de Zaragoza,Marı´a de Luna s/n,50018Zaragoza,Spain c Dept.d’Informa`tica i Enginyeria Industrial,Universitat de Lleida,Jaume II 69,25001Lleida,Spain Received 12February 2004Available online 16December 2004AbstractThe use of phase change materials (PCMs)for thermal storage in buildings was one of the first applica-tions studied,together with typical storage tanks.An interesting possibility in building application is the impregnation of PCMs into porous construction materials,such as plasterboard or concrete,to increase thermal mass.The thermal improvements in a building due to the inclusion of PCMs depend on the cli-mate,design and orientation of the construction,but also to the amount and type of PCM.Therefore,these projects require a complete simulation of the thermal behaviour of the designed space in the conditions of use established a priori.In this paper a simple methodology for the energetic simulation of buildings including elements with PCMs using the program TRNSYS is presented and validated.This procedure does not aim a simulation of the real transfer processes inside the materials with PCM,but to evaluate the influence of walls/ceiling/floor with PCM in the whole energy balance of a building.The key parameter in the simulations is the equivalent heat transfer coefficient which has to be determined for each material.Experimental evaluation1359-4311/$-see front matter Ó2004Elsevier Ltd.All rights reserved.doi:10.1016/j.applthermaleng.2004.11.001*Corresponding author.Tel.:+34973702742;fax:+34973702702.E-mail addresses:m.ibanez@macs.udl.es (M.Iba ´n ˜ez),bzalba@unizar.es (B.Zalba),lcabeza@diei.udl.es (L.F.Cabeza).1Tel.:+34973702538;fax:+34973702613.2Tel.:+34976762566;fax:+34976762189./locate/apthermengApplied Thermal Engineering 25(2005)1796–1807M.Iba´n˜ez et al./Applied Thermal Engineering25(2005)1796–18071797 of the coefficient is presented.The methodology is applied in a building such as a prototype room built with concrete panels with PCM.Ó2004Elsevier Ltd.All rights reserved.Keywords:Simulation;Phase change material(PCM);Thermal energy storage(TES);TRNSYS1.IntroductionThe use of phase change materials(PCMs)for thermal storage in buildings was one of thefirst applications studied,together with typical storage tanks[1].The former application of PCMs de-scribed in the literature was their use for heating and cooling in buildings,by Telkes in1975[2] and Lane in1986[3].The use of building material for thermal storage was pointed out already in 1975by Barkmann and Westtling[4]and later by other authors.An interesting possibility in building application is the impregnation of PCMs into porous con-struction materials,such as plasterboard or concrete,to increase thermal mass.The use of PCMs to store coolness have been developed for air conditioning applications,where cold is collected and stored from ambient air during night,and its relieved to the indoor ambient during the hottest hours of the day.This concept is known as free cooling(Zalba[5],Vakilaltojjar and Saman[6,7], Bruno and Saman[8]).In the last decade the integration of PCMs in building walls has regained interest and several projects are going on at the moment(Mehling et al.[9]).For each application,before the con-struction phase,the most adequate melting temperature of the PCM,the percentage of PCM to mix in the mortar with conventional materials,or the position of panels with PCM in the build-ing depending on its use and architectonic characteristics of the buildings,must be considered. The optimization of these parameters is fundamental to demonstrate the possibilities of success of the PCMs in building materials.Like in many other technologies,the success of the product depends more in the way of use than in the product itself.The thermal improvements in a building due to the inclusion of PCMs depend on the climate,design and orientation of the construction and operation of the building,but also to the amount and type of PCM.Therefore,these projects require a complete simulation of the thermal behaviour of the designed space in the conditions of use established a priori.Nowadays,there are different commercial programs for the thermal simulation of buildings: EnergyPlus,TRNSYS15,ESP-r,RADCOOL,DOE-2,I DA-I CE3,HVACSim,CLI M2000,and many others.Some studies done with these programs,like the one presented by Natural Re-sources Canada(NCR[10])outline the threefirst ones for their versatility and reliability. Although all the possibilities of these programs,none of them have modules that allow direct simulation of the effect of adding a PCM in a wall or window.However,they include algorithms to simulate active walls with tubes including a circulatingfluid.The temperature of the liquid compared to the internal ambient drives the surfaces to radiative heating or cooling of the indoor spaces.At the same time,while analytical models of several PCM building elements are available, very few authors have worked on the simulation of the effect of PCMs in buildings using whole thermal building simulation programs(Peippo et al.[11],Feustel and Stetiu[12],Jokisalo et al.1798M.Iba´n˜ez et al./Applied Thermal Engineering25(2005)1796–1807[13],Schossig et al.[14]).Peippo et al.[11]were one of thefirst to discuss the use of PCMs walls for short-term heat storage in a building simulation environment.In their proposal all surfaces of the south-facing direct-gain room excluding thefloor were covered by PCM panels.The PCM considered was fatty acid impregnated into conventional13mm-thick plasterboard.The energy simulation balances were analyzed by the code FHOUSE(Aro-Heinila¨and Sunanen[15]).Owing to computational limitations,the effect of latent heat of the PCM was accounted for by defining an effective specific heat capacity.The project from Feustel and Stetiu[12]studied the use of PCM imbedded in gypsum wallboards.A functional description of the specific heat was implemented into some of the wall modules available for the program RADCOOL(Stetiu et al.[16]).The paper by Jokisalo et al.[13]include the model of a concrete wall that contains macroencapsulated PCM, that is,tubesfilled with a hydrated salt.The mathematical model of this wall is included to the component of TRNSYS14.2(Beckman et al.[17])that simulates the behaviour of a single room. These algorithms cannot be easily included in simulations of more complex buildings with different zones.The project from Schossig et al.[14]is about microencapsulated PCM mixed with gypsum for interior wall application.The authors implemented the possibility to calculate non-linear thermal properties of construction materials in the simulation environment ESP-r(Clarke [18]).Therefore,the aim of this work is to present and compare a methodology that allows to easily simulating using a standard program the effect of the inclusion PCMs in the elements of a build-ing.The objective is not to develop a strict model of the wall to explain its thermal behaviour.The construction materials have to be characterized previously in a laboratory.The goal is to have a tool that allowed the analysis of the thermal effect of these materials in the building as a whole. Within this general objective,it is interesting for the methodology to allow:•The inclusion of materials with PCM in walls,ceiling and/orfloor.•The possibility of an easy definition of the thermal behaviour of these materials,once they are well characterized.•The characteristics of the materials with PCM located in different parts of the building can vary with the inclusion of different PCMs and in different percentages.Due to its versatility for the complete simulation of a building,to the analysis done by the I EA (2003)[19]for radiative construction elements,and to the possibilities of connection of the sim-ulation module of a building with other installations,solar or HVAC,the program TRNSYS15is selected as base tool for the purpose.TRNSYS is an acronym for aÔtransient simulation programÕand is a quasi-steady simulation model.This program was developed at the University of Wiscon-sin by the members of the Solar Energy Laboratory(Beckman et al.[17]).2.MethodologyOne of the components to simulate building thermal behaviour in TRNSYS is Type56ÔMulti-Zone buildingÕ.This component model deals with the thermal balances of a building having up to 25thermal zones.The building model in Type56is a non-geometrical balance model with one air node per zone,representing the thermal capacity of the zone air volume and capacities that areM.Iba´n˜ez et al./Applied Thermal Engineering25(2005)1796–18071799 closely connected like furniture with the air node.Separate equipment components can be coupled to the zones as either internal convective gains or ventilation gains.In order to use Type56a separate pre-processing program PREBID is executed.The PREBID program reads in and processes afile containing the building description and generates twofiles that are used by the Type56component during a TRNSYS simulation.The inputs and outputs of Type56depend upon the building description and options within the PREBID program. Thermally active building elements are used to condition buildings by integrating afluid system into massive parts of the building itself.Examples are radiantfloor heating or cooling systems, radiant ceilings or wall heating or cooling systems,all well known.To take into account the behaviour of radiant heating and cooling in dynamic simulation programs specific models or modelling methods have been proposed in TRNSYS15.Koschenz and Lehmann[20]developed a powerful method for modelling thermo-active construction element systems and integrated it in the multi-zone building model TYPE56of TRNSYS15.In the integrated model the heat con-duction through the element is reduced to a one-dimensional form by applying resistance models. Thereby,the existing transfer function method of the building model TYPE56for walls can be used for solving the one dimensional heat conduction problem.The developed theory can be ap-plied for dynamic simulation.The model is defined easily within the building description as a wall with a so-called active layer.As input data for the active layer geometric data andfluid data are required.But an expert mode is available in which an equivalent heat transfer coefficient is defined by the user.Due to the thermal behaviour and applications analogies(free cooling,free heating)between the radiative active walls and those including PCM,it seems adequate to simulate walls including PCM as a differentiate type of active system.The methodology here presented consists in giving to the TRNSYS program the characteristics of a wall with PCM to a standard active wall. Essentially,the wall with PCM keeps its temperature approximately constant in the central part during the phase change of the PCM,and the thermal conductivity of the wall can be a function of the temperature.These behaviours are easily simulated in TRNSYS using walls with active layers with the proper external control.Only ultra-pure paraffins melt and freeze sharply at a given temperature but mixtures of PCM show a region of temperatures where melting takes place,if desired the functions for specific enthalpy can also be introduced to Type56active layers [12].To simulate that the storage and release of energy,the control of thefluidflow and temperature of the active layer in Type56is suggested.When the active layer reaches the PCM phase change temperatures,the circulation of thefluid at the phase change temperature is imposed in the simulation:•for the energy storage in the active layer with PCM,with an ambient with higher temperature, the circulatingfluid will release thermal energy of the wall giving an analogue thermal effect to the melting of PCM in a solid–liquid phase change and the storage in the PCM,until the given maximum storage capacity is reached,•for the energy release from the active layer with PCM,with an ambient with lower temperature, the circulatingfluid will store energy in the wall at the phase change temperature,in a similar way to the solidification of the PCM,until all the previously stored energy is released and all the PCM is solid,and1800M.Iba´n˜ez et al./Applied Thermal Engineering25(2005)1796–1807•usually,partial charge and discharge processes of the PCM occur without reaching the maxi-mum storage capacity or complete discharge;then,the liquidflux at the PCM phase change temperature do not stop.Together with the circulating waterflow and temperature in the active layer,a third fundamen-tal element in the simulation is the equivalent heat transfer coefficient.This parameter,that can be defined by the user and introduced in each step of the simulation,is the one that really character-izes the operative way of the thermal behaviour of the wall with PCM,because it allows to give to the simulation the rate at which the thermal energy transfer processes due to the storage material occur.TRNSYS15allows controlling the Type56in the simulation through modules connected to it. Standard TRNSYS modules can be used to control Type56introducing the necessary active wall temperature functions.For simplicity of the whole project,in the presented method one of the controllers included in the standard package of TRNSYS was modified generating a new one, from now on called Type222.This subprogram will determine in each step of the simulation the enthalpy of the PCM,its temperature and the variations with the previous simulation step. Depending on these parameters,with Type222theflow and temperature of thefluid inside the tubes of the active wall,and the equivalent heat transfer coefficient are calculated and Type 222acts on Type3and Type56.Once all the components on a TRNSYS system have been identified and a mathematical description of each component is available,it is interesting to construct theflow diagram system.A simplified informationflow diagram for the building with PCM is shown in Fig.1.As it can be seen in Fig.1,the main component of the TRNSYS deckfile constructed for this purpose are Type56and Type222.Additional components required are a Type9data reader,Type16radi-M.Iba´n˜ez et al./Applied Thermal Engineering25(2005)1796–18071801 ation processor,Type3pump,Type33psychometrics,Type69sky temperature,Type93input value recall,and Type55and Type5for treatment of the output data.The working way of Type56in the diagram of Fig.1is not different from those corresponding to other building simulations with active layers.There are three inlets,related to the active layer, for each wall/ceiling/floor containing PCMs:inlet temperature offluid in the active layer,inlet massflow rate in the active layer and user-defined equivalent heat transfer coefficient.The outlets are stored in Type93and simultaneously introduced in Type222.Four outlets,to evaluate element temperature and enthalpy,are given for each wall/ceiling/floor with PCM:node temperature of active layer,inside surface temperature,outside surface temperature and energy input byfluid of active layer to zone.3.Experimental validationUsing the operative methodology proposed in the previous section it is possible to evaluate the PCM behaviour in a wall without simulating the real heat transfer processes.An empirical justi-fication is given in this section.The validation has been planned using a concrete block with5%kg PCM/kg concrete.The ther-mophysical properties of the PCM microencapsulated used MICRONALÒcan be obtained from the manufacturer BASF.The dimensions of the sample block are8cm·8cm·15cm.To perform the experimental tests,an energy storage test rig built in the University of Zaragoza was used(Fig.2)[5].This test rig is an air closed loop that goes inside a chamber where the mate-rial to be tested islocated.1802M.Iba´n˜ez et al./Applied Thermal Engineering25(2005)1796–1807The laboratory test is conducted in the following way.The sample temperature is initially homogeneous,around18°C.Just one side of the block is not thermally insulated,therefore the heat transfer in the block is unidimensional.This side(8cm·8cm)is placed in the space with air at constant temperature(above30°C).Then energy transfer from the surface in contact with the air to the opposite side of the block is related to the thermal properties of the sample.The opposite surface,15cm far away,is defined hereafter as the control surface.This control surface temperature and the air temperature are measured ter,1min time averages are studied.According to the methodology proposed in this paper,the laboratory test is simulated using the Type56of TRNSYS15under the proper control.Thefirst step is to define the material for the wall in Type56using the thermophysical parameters previously determined of the concrete block PCM5%.This amount of PCM is estimated from previously published data in other applications [14].The density of the concrete with PCM5%was estimated as2050kg mÀ3,the thermal conduc-tivity1.0W mÀ1KÀ1and the heat capacity800J kgÀ1KÀ1.The second step is to simulate the PCM effect;therefore an active layer has to be introduced to model the heat storage capacity of the wall.The active layer control is done using three inputs defined in Type56:circulating waterflow and temperature in the active layer,and the equivalent heat transfer coefficient.A high waterflow is selected to avoid the influence of this parameter.The circulatingfluid temperature is determined according to MICRONALÒcharacteristics.Waterflow is turned on or offto simulate the maximum heat storage capacity defined according to the PCM content and its phase change enthalpy.The equivalent heat transfer coefficient is the key parameter unknown.It has to be determined for each new composite material.The simulation of the test has been done using different values of the key parameter.Simulated temperatures in the control surface have been compared to measured parison has been done computing the RMSE of measured and simulated data for thefirst3h of test.Table1is a summary of the results.The minimum RMSE,0.39,is obtained using an equivalent heat transfer coefficient of10W mÀ2KÀ1.Hereafter,10W mÀ2KÀ1is chosen as the reliable value to simulat-ing concrete block MICRONALÒ5%using the methodology developed.Fig.2shows the temperatures of control surface measured and simulated using the equivalent heat transfer coefficient of10W mÀ2KÀ1.Agreement between experimental and simulated data is really good.In the same graph the air heated temperature is plotted.It is also drawn the temper-ature of control surface simulated without using the active layer approach,assuming a wall with-out latent heat storage.Simulated and measured control surface temperatures tend to the air temperature.The simulated temperatures without PCM demonstrate the lower thermal inertia of this wall.It is proven that it is possible tofind an equivalent heat transfer coefficient that makes suitable the simulation using TRNSYS of building components incorporating PCM.Though in this test a constant equivalent heat transfer coefficient has given accurate results it is not discarded that for Table1Comparison of measured and modelled temperature values for different equivalent heat transfer coefficients Equiv.heat transfer coefficient(WmÀ2KÀ1)5102550100 RMSE(°C)0.500.39 1.03 1.54 2.17M.Iba´n˜ez et al./Applied Thermal Engineering25(2005)1796–18071803 different materials or in different temperature ranges a temperature dependent coefficient could be needed.4.ApplicationThe presented methodology has been applied to the discussion of the characteristics of a pro-totype of a room developed within the MOPCON project.This construction is done with concrete panels that include PCM(Fig.3).The presented results cannot be generalized and are only an example of application.Ultimately,the effect of PCM storage must be evaluated in each case application,taking into account the climate,the construction,and the operation of the building. Here,the simulations done were located in Lleida,using hourly data of temperature,humidity and solar radiation for the average year during June,July and August[21].Within the project MOPCON,the goal of the analysis was an economical optimization of the use of the PCM,therefore the following three variables were considered:•the panels including PCM can be installed in one or more walls,ceiling andfloor,•the thermal storage capacity by volume unit in the panels varies as function of the percentage of PCM included,and•the phase change temperature of the PCM was also discussed.I n this work,also the different possible dimensions of the prototype room were studied,with the same structure of Fig.3.The results of this fourth variable are not presented here.The combina-tion of the considered variables,shown in Fig.4,gives200alternatives that needed comparison by simulation.Due to the application within the considered project,free cooling,for the evaluation of the ef-fect of the panels with PCM,the selected parameter of interest is the indoor air temperature in the prototype room.The difference of the maximum temperature with and without PCM is calculated daily.The average of these differences during the studied period of three months is considered a good indicator of the answer of the prototype room to the inclusion of PCM.As example,some of the results are presented here.Fig.5shows the maximum temperature of the prototype room during July for some configurations.The PCM was considered to be included only in the ceiling,and two phase change temperatures were compared (25and 30°C),combined with two thermal storage densities (15,000kJ m À3and 60,000kJ m À3).The graphical result al-ready shows that a phase change temperature around 25°C would be the most interesting.Table 2presents the results of the most interesting alternatives of the average of the difference between daily maximum temperatures in the (Fig.6)prototype room with PCM and a prototype room withoutPCM.Fig.4.Prototype room sketch.1804M.Iba ´n ˜ez et al./Applied Thermal Engineering 25(2005)1796–1807M.Iba´n˜ez et al./Applied Thermal Engineering25(2005)1796–18071805Table2Average of the difference between maximum daily temperatures for several alternatives(°C)Ceiling West wall Ceiling+south wall Ceiling+west wall 25°C—5000kJ mÀ30.770.300.84 2.5725°C—37,500kJ mÀ3 1.59 1.03 2.13 2.9225°C—60,000kJ mÀ3 1.98 1.11 2.68 3.5830°C—15,000kJ mÀ30.780.500.62 1.6330°C—37,500kJ mÀ3 1.130.81 1.78 2.6430°C—60,000kJ mÀ3 1.53 1.18 2.35 3.021806M.Iba´n˜ez et al./Applied Thermal Engineering25(2005)1796–1807The study of the prototype room using the simulation program TRNSYS allows to obtain information for future designs and applications.To minimize the quantity of used PCM and, therefore the production costs of the panel,but to get an interesting effect of reduction of maxi-mum temperatures,the following recommendations should be followed:1.The PCM should be included in the ceiling and west wall of the prototype room.2.The needed storage capacity of the panels for the maximum air temperature to be reducedenough to be measured is around15,000kJ mÀ3and37,500kJ mÀ3.3.The used PCM for the climatic conditions and the design of this application should have aphase change temperature between25°C and27.5°C.With these considerations,an average maximum ambient temperature decrease up to3°C would be obtained.5.ConclusionA simple methodology for the energetic simulation of buildings including elements with PCMs with the program TRNSYS is presented.The method uses the simulation possibilities of active layers for radiative heating and cooling of the Type56of TRNSYS15.The control of the behaviour of the active layer must be done from the exterior of Type56.This proce-dure does not aim a simulation of the real transfer processes inside the materials with PCM, but to evaluate the influence of walls/ceiling/floor with PCM in the whole energy balance of a building.The method is validated in a laboratory experience using concrete that incorporates PCMs.The equivalent heat transfer coefficient is a key parameter which has to be evaluated for each material. The coefficient is related to the heat transfer rate between the PCM microencapsulated and the concrete.The suitability of the methodology has been proven when the proper equivalent heat transfer coefficient is used.The methodology was used in a building such as a prototype room built with concrete panels with PCM.The simulations showed interesting results for the determination of the PCM in walls/ceiling/floor,storage capacity of the panels with PCM,and the optimum phase change temperature used.Although the methodology requires more experimental validation,it can already be concluded that it is a good tool for discussion of the application of PCMs in buildings.AcknowledgmentsThe present work was developed under MOPCON EU CRAFT Project G5ST-2002-50331.The authors would like to acknowledge ASPICA Constructora S.A.(Spain)and B.S.A.Arquitectura y Gestio´n S.L.(Spain)for the design of the cubicle,and all the other partners in the project for their help and contributions:PROKEL S.A.(Greece),MEDYSYS(France),I NTRON B.V.(Nether-lands)and Fundacio´n INASMET(Spain).References[1]B.Zalba,J.M.Marı´n,L.F.Cabeza,H.Mehling,Review on thermal energy storage with phase change:materials,heat transfer analysis and applications,Appl.Thermal Eng.23(2003)251–283.[2]M.Telkes,Thermal storage for solar heating and cooling,in:Proceedings of the Workshop on Solar Energy Storage Subsystems for the Heating and Cooling of Buildings,Charlottesville,VA,USA,1975.[3]ne,Solar Heat Storage:Latent Heat Material,Technology,vol.,CRC Press,Florida,1986.[4]H.G.Barkmann,F.C.Wessling,Use of buildings structural components for thermal storage,in:Proceedings of the Workshop on Solar Energy Storage Subsystems for the Heating and Cooling of Buildings,Charlottesville,VA,USA,1975.[5]B.Zalba,Almacenamiento te´rmico de energı´a mediante cambio de fase,Procedimiento experimental,Ph.D.Thesis,University of Zaragoza,Spain,2002.[6]S.M.Vakilaltojjar,W.Saman,Analysis and modelling of a phase change storage system for air conditioning applications,Appl.Thermal Eng.21(2001)249–263.[7]S.M.Vakilaltojjar,W.Saman,Domestic heating and cooling with thermal storage,in:Proceedings of Terrastock 2000,Stuttgart,Germany,2000,pp.381–386.[8]F.Bruno,W.Saman,Testing of a PCM energy storage system for space heating,in:Proceedings of the World Renewable Energy Congress WI ,Cologne,Germany,2002.[9]H.Mehling,S.Hiebler,L.F.Cabeza,News on the application of PCMs for heating and cooling of buildings,I EA,ECES I A,Annex 17,Advanced Thermal Energy Storage Through Phase Change Materials and Chemical Reactions—Feasibility Studies and Demonstration Projects,3rd Workshop,Tokyo,Japan,2002.[10]NRC,Defining the methodology for the next-generation HOT2000simulator.Available at www.buildings-group.nrcan.gc.ca/docs/pdf/final_report_survey.pdf ,1998.[11]K.Peippo,P.Kauranen,P.D.Lund,A multicomponent PCM wall optimised for passive solar heating,EnergyBuildings 17(1991)259–270.[12]H.E.Feustel,C.Stetiu,Thermal performance of phase change wallboard for residential cooling application,Report LBL-38320,Lawrence Berkeley National Laboratory,1997.[13]J.Jokisalo,mberg,K.Sire´n,Thermal simulation of PCM structures with TRNSYS,in:8th nternational Conference on Thermal Energy Storage,Stuttgart,Germany,2000.[14]P.Schossig,H.-M.Henning,T.Haussman,A.Raicu,Encapsulated phase-change materials integrated intoconstruction materials,in:Proceedings of the 9th I nternational Conference on Thermal Energy Storage—Futurestock Õ2003,Warsaw,Poland,2003.[15]V.Aro-Heinila ¨,M.Suvanen,Simulation program for energy analysis of multiroom houses for solar energy studies,Report TKK-F-A436,Helsinki University of Technology,1980.[16]C.Stetiu,H.E.Feustel,F.C.Winkelmann,Development of a model to simulate the performance of hydronicradiant cooling ceilings,ASHRAE Trans.101(1995)730–743.[17]W.A.Beckman et al.,TRNSYS,Reference manual,vol.2,Solar energy Laboratory,Madison,USA,2001.[18]J.A.Clarke,Energy simulation in building design,Adam Hilger Ltd.,1985.[19]I EA,RADTest—Radiant heating and cooling test cases,A Report of Task 22,subtask C,Building EnergyAnalysis Tools Comparative Evaluation Tests,I nternational Energy Agency,2003.[20]M.Koschenz,B.Lehmann,Handbuch thermoaktive Bauteilsysteme TABS,EMPA Abteilung Energiesysteme/Haustechnik,CH-8600Du ¨bendorf,2000.[21]M.Iba ´n ˜ez,L.F.Cabeza,An approach to the simulation of PCMs in building applications using TRNSYS,in:Proceedings of the III International TRNSYS Users Õday,Barcelona,Spain,2004.M.Iba ´n ˜ez et al./Applied Thermal Engineering 25(2005)1796–18071807。

相关文档
最新文档