High Temperature Resummation in the Linear $delta$-Expansion

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降温速率对梨瓜细胞冻干特性的影响

降温速率对梨瓜细胞冻干特性的影响

张哲,郎元路,吴巧燕,等. 降温速率对梨瓜细胞冻干特性的影响[J]. 食品工业科技,2022,43(19):31−42. doi: 10.13386/j.issn1002-0306.2021120035ZHANG Zhe, LANG Yuanlu, WU Qiaoyan, et al. Effect of Cooling Rate on Freeze-drying Characteristics of Pear Melon Cells[J].Science and Technology of Food Industry, 2022, 43(19): 31−42. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2021120035· 研究与探讨 ·降温速率对梨瓜细胞冻干特性的影响张 哲*,郎元路,吴巧燕,张志强,陈佳楠,计宏伟,田津津(天津商业大学机械工程学院,天津 300134)摘 要:为了探究降温速率对梨瓜细胞冻干过程中的影响,基于低温显微镜成像及真空冷冻干燥技术,对梨瓜细胞进行了不同降温速率(5、15、25、35、50 ℃/min )下的冻干可视化实验,分析了脱水干燥过程中的细胞形态学参数(当量直径、面积、周长、体积)以及内压在冻干过程中的变化规律,并对干燥组织的多孔物料特征参数(孔隙率)进行了研究。

结果表明:冻结温度随着降温速率的增长整体呈逐渐降低的趋势;冻干过程中,降温速率为25 ℃/min 时,细胞形态学参数和内压变化最小,其中,细胞形态学参数变化率与内压均随降温速率的增大呈先减小再缓慢增加的趋势;过高和过低的降温速率下,梨瓜细胞形态与内压变化较大,不利于梨瓜的冻干处理;当降温速率大于5 ℃/min 时,孔隙率较大且受降温速率的影响较小,只在一定范围内发生微小波动;梨瓜的最佳降温速率为25 ℃/min ,该降温速率下的细胞形态及溶质损害最小。

英语作文要求温度高

英语作文要求温度高

英语作文要求温度高High Temperature。

Temperature is an important factor that affects our daily lives. It can bring both comfort and discomfort depending on its level. In this essay, we will discuss the topic of high temperature and its impact on various aspects of our lives.High temperature refers to a condition where the level of heat in the environment is significantly above the average. This can occur during summer months or in regions with a tropical climate. When the temperature rises, it can have both positive and negative effects on different aspects of our lives.One of the positive impacts of high temperature is the ability to enjoy outdoor activities. During summer, people can engage in various outdoor sports such as swimming, hiking, and playing beach volleyball. The warm weathercreates a pleasant atmosphere for these activities,allowing individuals to spend quality time with friends and family. Moreover, high temperature can also be beneficialfor agriculture. Certain crops thrive in warm weather, and farmers can take advantage of this by cultivating heat-loving plants such as tomatoes, peppers, and watermelons.However, high temperature also brings severalchallenges and negative consequences. One of the most significant issues is the health risks associated with extreme heat. Heatwaves can lead to heatstroke, dehydration, and other heat-related illnesses. The elderly, young children, and individuals with pre-existing medical conditions are particularly vulnerable to these risks. Additionally, high temperature can worsen air pollution.The combination of heat and stagnant air can trap pollutants, leading to poor air quality. This can have adverse effects on respiratory health and can exacerbate conditions such as asthma and allergies.Furthermore, high temperature can also impact the economy and infrastructure. In regions where hightemperatures are not the norm, the sudden increase in heat can strain the power grid. Air conditioners and othercooling systems consume a significant amount of electricity, and the increased demand can lead to power outages. Moreover, extreme heat can damage roads, railways, andother infrastructure. Asphalt can soften and deform under high temperatures, causing cracks and potholes. This not only affects transportation but also requires costly repairs.To mitigate the negative effects of high temperature, several measures can be taken. Firstly, it is crucial to raise awareness about the health risks associated with extreme heat. This can be done through educational campaigns and public service announcements. People shouldbe encouraged to stay hydrated, seek shade, and avoid prolonged exposure to the sun during peak hours. Secondly, urban planning can play a significant role in reducing the impact of high temperature. The construction of green spaces, parks, and the planting of trees can help cool down urban areas and improve air quality. Additionally, the useof reflective materials in buildings and roads can reduceheat absorption and lower temperatures.In conclusion, high temperature has both positive and negative effects on various aspects of our lives. While it allows for enjoyable outdoor activities and benefits agriculture, it also poses health risks, worsens air pollution, and affects the economy and infrastructure. By taking necessary precautions and implementing appropriate measures, we can mitigate the negative consequences of high temperature and create a more comfortable and sustainable environment for all.。

High Temperature Rheological Characteristics of Brucite Fiber Modified Asphalt Mastics

High Temperature Rheological Characteristics of Brucite Fiber Modified Asphalt Mastics

High Temperature Rheological Characteristics of Brucite Fiber ModifiedAsphalt MasticsBowen Guan1,a,Shuanfa Chen2,Rui Xiong1, Yanping Sheng2 and Lili Ma2 1Key Laboratory for Special Area Highway Engineering of Ministry of Education,Chang’ anUniversity, Xi’ an 710064, China2School of Materials Science and Engineering, Chang’an University, Xi’an 710061, Chinaa guanbowen2001@Keywords: Brucite fiber, Asphalt mastic, Rheological characteristic.Abstract. The rheological properties of brucite fiber asphalt mastics are studied by the Brookfield viscosity test in this paper. The results show that at 105℃ and 120℃, brucite fiber asphalt mastics shows the characteristics of non-Newtonian fluid. At 135℃ and 150℃, it shows the characteristics of Newtonian fluid gradually. When the temperature is higher than 150℃, the asphalt mastics has fully manifested the characteristics of Newtonian fluid. The viscosity increases with the increasing of the dosage of brucite fiber. The value of ZSV increases with the increasing of the dosage of brucite fiber. According to the change law of ZSV, the anti-rutting performance of asphalt mastics is improved by the addition of brucite fiber.IntroductionBrucite fiber asphalt concrete is a pavement composite material, whose performance can be improved by the addition of brucite fiber [1]. Compared with the other modification methods, the cracks such as the temperature shrinkage crack and the reflective crack in the asphalt concrete can be prevented and the damage of rutting deformation and fatigue can be reduced [2]. It plays a prominent role in improving the quality and extending service life of asphalt concrete [3]. As a new type of pavement material, high temperature rheological characteristics of brucite fiber modified asphalt mastics has not been reported at home and abroad. Therefore, the rheological properties of brucite fiber asphalt mastics are studied by the Brookfield viscosity test in this paper.ExperimentalRaw materials. SBS modified asphalt is used in the research. Table 1 shows the test results of asphalt (JTJ052-2000, 2000).Table 1 Test Results of SBS modified asphaltItemsPenetration[(100g, 5s,25℃)/0.1mm]Ductility[(5℃)/cm]Softeningpoint [℃]Residue after RTFOTMass lossPenetrationratio of[25℃/%]Ductility[(5℃)/cm]SBS 71 48 89.5 -0.02 68.9 24The grade 7 of brucite fiber, which is produced from mine tailings, is used in the paper. Brucite fiber mine is rare in the world. However, it is abundant in China, whose reserve is total 780 million tons. Brucite fiber is quite different from asbestos in chemical compositions, crystal structures, and chemical properties. The physical properties is listed in Table 2. From Table 2, it can be seen that brucite fiber have the high tensile strength.Table 2 Physical properties of brucite fiberItems Density [ g/cm3] Tensile strength [Mpa] Young’s modulus [Gpa] Brucite 2.4 932 14.7–19.6Test Methods.To evaluate the high temperature rheological characteristics of brucite fiber modified asphalt mastics, Brookfield viscosity test is performed are tested according to the ASTM D 4402 standard method.Test results and discussionBrucite fiber asphalt mastics with four different dosages (0%, 2%, 4% and 6%) are tested in different temperature (105℃, 120℃, 135℃, 150℃). Test results are showed in Table 3, Table 4, Table 5 and Table 6.Table 3 Viscosity Results of asphalt mastics in 105℃Dosage ( brucite fiber : asphalt)6:100 4:100 2:100 0:100Speed [r/min] Viscosity[Pa·s]Speed[r/min]Viscosity[Pa·s]Speed[r/min]Viscosity[Pa·s]Speed[r/min]Viscosity[Pa·s]0.3 91.667 0.3 71.667 0.3 45.21 1.5 19.667 0.5 82 0.5 70.5 0.5 44.95 2 190.6 80 0.6 69.083 0.6 43.33 2.5 181 72.5 1 60.75 1 40.86 3 17.751.5 67.667 1.5 55.5 1.5 37.98 4 16.9382 62.5 2 51.375 2 34.23 5 16.32.5 58.3 2.5 48.5 2.5 33.48 6 15.6253 52.667 3 46.417 3 30.15 10 13.94 47.75 4 43.187 12 13.3125 44.7 5 40.46 38.7080.3 71.667Table 4 Viscosity Results of asphalt mastics in 120℃Dosage ( brucite fiber : asphalt)6:100 4:100 2:100 0:100Speed [r/min] Viscosity[Pa·s]Speed[r/min]Viscosity[Pa·s]Speed[r/min]Viscosity[Pa·s]Speed[r/min]Viscosity[Pa·s]0.5 20.000 0.5 14.500 10.0 7.450 10.0 -1.0 18.000 1.0 13.750 12.0 7.375 12.03.7291.5 16.667 1.5 13.167 20.0 7.075 20.0 3.5502.0 15.750 2.0 12.750 30.0 6.783 30.03.4002.5 15.000 2.5 12.400 50.0 6.400 50.03.2053.0 14.500 3.0 12.000 60.0 6.2754.0 13.813 4.0 11.6255.0 13.200 5.0 11.2006.0 12.750 6.0 10.91710.0 11.600 10.0 10.10012.0 11.187 12.0 9.81220.0 10.163 20.0 9.025Table 5 Viscosity Results of asphalt mastics in 135℃Dosage ( brucite fiber : asphalt)6:100 4:100 2:100 0:100Speed [r/min] Viscosity[Pa·s]Speed[r/min]Viscosity[Pa·s]Speed[r/min]Viscosity[Pa·s]Speed[r/min]Viscosity[Pa·s]1.5 6.667 1 5.25 302.467 30 1.158 3 5.75 1.5 5 50 2.43 50 1.135 5.2 2 4.75 60 2.4 60 1.1176 5 3 4.417 100 2.335 100 1.09 10 4.55 4 4.2512 4.396 5 4.120 4.025 6 430 3.725 10 3.72550 3.41 12 3.62560 3.35 20 3.41230 3.20850 2.995Table 6 Viscosity Results of asphalt mastics in 150℃Dosage ( brucite fiber : asphalt)6:100 4:100 2:100 0:100Speed [r/min] Viscosity[Pa·s]Speed[r/min]Viscosity[Pa·s]Speed[r/min]Viscosity[Pa·s]Speed[r/min]Viscosity[Pa·s]2.5 2.9 1 3 50 1.17 50 0.544 2.688 2 2.625 60 1.158 60 0.53755 2.5 3 2.417 100 1.13 100 0.52510 2.25 4 2.31312 2.188 5 2.2520 2.013 6 2.16730 1.9 10 1.97550 1.775 12 1.91760 1.729 20 1.763100 1.628 30 1.65850 1.55560 1.517100 1.43From Table 3, Table 4 Table 5 and Table 6, it can be seen that viscosity decreases with the increasing of the rotate speed at 105℃ and 120℃, which shows the characteristics of non-Newtonian fluid. The rotate speed has little effect on the viscosity at 135℃and 150℃, which shows the characteristics of Newtonian fluid gradually. It can be inferred that when the temperature is higher than 150℃, the asphalt mastics has fully manifested the characteristics of Newtonian fluid and the viscosity is no longer affected by the rotate speed. It can be seen that the viscosity increases with the increasing of the dosage of brucite fiber.Among all the results, the viscosity can be characterized with the rotate speed in the test, and the rotate speed can be used as an independent variable in the regression Equation 1.η=αv+β (1) Where: η— Viscosity, Pa·s; v — Rotate speed, r/min; α — gradient of the formula; β — the constant coefficient of the formula.Through regression analysis of the test, the regression formula can be got in Table 7. Recently there has been considerable interest, especially in Europe, in the use of zero shear viscosity (ZSV) as a specification criterion for asphalt mastics. The equation used enables the calculation of zero-shear viscosity η from viscosity measurements conducted under various shear conditions, that is, with rotational viscometer at different shear rates.Table 7 Regression equations and ZSV of asphalt masticsDosage Temperature Regression equation CorrelationcoefficientZSV6:100 105 η= -9.393v + 85.13 0.909 85.13 120 η= -0.686v + 17.24 0.993 17.24 135 η= -0.282v + 5.479 0.986 5.479 150 η= -0.107v + 2.249 0.970 2.2494:100 105 η= -3.535v + 68.11 0.947 68.11 120 η= -0.452v + 13.35 0.984 13.35 135 η= -0.180v + 4.136 0.984 4.136 150 η= -0.080v + 1.826 0.978 1.8262:100 105 η= -5.685v + 46.87 0.984 46.87 120 η= -0.023v + 7.607 0.972 7.607 135 η= -0.001v + 2.521 0.990 2.521 150 η= -0.000v + 1.206 0.988 1.2060:100 105 η= -0.574v + 19.65 0.943 19.65 120 η= -0.011v + 3.812 0.962 3.812 135 η= -0.000v + 1.180 0.955 1.180 150 η= -0.000v + 0.555 0.998 0.555From Table 7, it can be seen that the value of ZSV increases with the increasing of the dosage of brucite fiber at the same temperature. With the decreasing of the temperature, the value of ZSV is improved significantly. So the anti-rutting performance of asphalt mastics is improved by the addition of brucite fiber.Conclusions(1) At 105℃ and 120℃, brucite fiber asphalt mastics shows the characteristics of non-Newtonian fluid. At 135℃and 150℃, it shows the characteristics of Newtonian fluid gradually. When the temperature is higher than 150℃, the asphalt mastics has fully manifested the characteristics of Newtonian fluid.(2) The viscosity increases with the increasing of the dosage of brucite fiber.(3) According to the change law of ZSV, the anti-rutting performance of asphalt mastics is improved by the addition of brucite fiber.References[1] X. Ma, F.J. Ni and X. Gu: Journal of Highway and Transportation Research and Development,Vol. 23 (2006) No.1,p.24.[2] F. Dong, P. Wan, K. Zhou, J. Liu and S. Luo: Bull. Mineral. Petrol. Geochem, Vol. 16 (1997)No.1,p.43[3] R. Zheng, K. Wei: China Mines Ind, Vol. 7 (1998) No.2,p.21.Advanced Building Materials10.4028//AMR.250-253High Temperature Rheological Characteristics of Brucite Fiber Modified Asphalt Mastics10.4028//AMR.250-253.703。

高温测试的英文

高温测试的英文

高温测试的英文High Temperature TestingIntroductionHigh temperature testing is a crucial process in various industries, including automotive, aerospace, electronics, and materials testing. This test evaluates the performance and reliability of products and materials under extreme heat conditions. It helps manufacturers ensure that their products can withstand high temperatures, prevent failures, and maintain optimal functionality.Purpose of High Temperature TestingThe primary purpose of high temperature testing is to simulate real-world conditions and understand how products or materials behave when exposed to elevated temperatures. This testing ensures that the product meets customer expectations, complies with industry standards, and performs reliably even in extreme environments. Additionally, high temperature testing helps identify design flaws, manufacturing errors, and weak points that can result in failures or accidents.Methods of High Temperature TestingThere are several methods commonly used for high temperature testing:1. Ambient high temperature testing: In this method, the product or material is placed in a controlled environment with elevated temperatures. The temperature is gradually increased and maintained for a specific period to simulate long-term exposure. This method aims to evaluate the product's performance and reliability under constant high temperatures.2. Cycling high temperature testing: This method involves subjecting the product or material to alternating high and low temperatures. The temperature is cycled within a specific range for a defined number of cycles. This test helps assess the thermal fatigue resistance, dimensional stability, and the ability of the product to withstand repeated temperature changes.3. Rapid temperature change testing: This testing method involves exposing the product or material to rapid temperature changes. This process simulates sudden temperature fluctuations that may occur during transportation, start-up, or environmental conditions. It helps evaluate how the product responds to thermal shocks and assess its thermal stress resistance.4. Thermal gradient testing: In this method, a temperature gradient is created across the product or material. This test helps evaluate the thermal conductivity, heat transfer properties, and thermal stresses that occur due to temperature variations. Itprovides valuable information on how the product is affected by temperature gradients and helps optimize its design.Equipment Used in High Temperature TestingHigh temperature testing requires specialized equipment to create and control extreme heat conditions. Some commonly used equipment includes:1. Climatic chambers: These chambers have temperature control mechanisms that can simulate a wide range of high temperatures. They are designed to maintain a consistent temperature throughout the testing process.2. Ovens and furnaces: These are used to subject materials or small components to high temperatures for extended periods. Ovens are generally used for ambient high-temperature testing, while furnaces can reach higher temperatures and are suitable for materials testing.3. Thermal shock chambers: These chambers are used in rapid temperature change testing. They can quickly transition between hot and cold temperatures to simulate sudden thermal shocks.4. Thermal conductivity meters: These devices measure the thermal conductivity and heat transfer properties of materials. They are crucial in thermal gradient testing to evaluate how materials respond to temperature variations.Benefits of High Temperature TestingHigh temperature testing offers several benefits to manufacturers and consumers:1. Reliability and safety: Testing products and materials at high temperatures helps identify potential failures that may occur in extreme conditions. This ensures that the product performs reliably and safely, reducing the risk of accidents or malfunctions.2. Compliance with regulations and standards: Many industries have specific regulations and standards regardinghigh-temperature performance. Testing ensures that the product meets these requirements and avoids penalties or legal repercussions.3. Cost savings: Identifying design flaws or weak points during testing helps manufacturers make necessary improvements before mass production. This prevents costly recalls, warranty claims, and customer dissatisfaction.4. Enhanced product performance: High temperature testing helps manufacturers optimize product design and materials for better performance and durability under extreme conditions. This can lead to improved customer satisfaction and increased market competitiveness.ConclusionHigh temperature testing is a crucial step in ensuring the reliability, safety, and performance of products and materials. By subjecting them to extreme heat conditions, manufacturers canidentify weaknesses, make necessary improvements, and deliver high-quality products that meet customer expectations. This testing process plays a vital role in various industries, helping them comply with regulations, reduce costs, and provide superior products to consumers.。

气温攀升学术英语作文

气温攀升学术英语作文

气温攀升学术英语作文Title: The Escalation of Temperature: A Global Academic Perspective。

Introduction。

The escalation of temperature has emerged as a critical concern in contemporary discourse, transcending geographical boundaries and disciplinary confines. This essay delves into the multifaceted dimensions of rising temperatures, encompassing scientific, environmental, and societal implications.Scientific Understanding。

At the core of the discussion lies the scientific understanding of temperature escalation. Over the past century, anthropogenic activities, notably the combustion of fossil fuels and deforestation, have significantly contributed to the amplification of greenhouse gases in theatmosphere. These gases, including carbon dioxide and methane, trap heat, leading to a phenomenon known as the greenhouse effect. Consequently, global temperatures have witnessed a steady rise, manifesting in phenomena such as global warming and climate change.Environmental Ramifications。

High-temperature pH measuring during hot-water extraction of hemicelluloses from wood

High-temperature pH measuring during hot-water extraction of hemicelluloses from wood

Industrial Crops and Products 61(2014)9–15Contents lists available at ScienceDirectIndustrial Crops andProductsj o u r n a l h o m e p a g e :w w w.e l s e v i e r.c o m /l o c a t e /i n d c r opHigh-temperature pH measuring during hot-water extraction of hemicelluloses from woodJens Krogell a ,∗,Kari Eränen b ,Kim Granholm c ,Andrey Pranovich a ,Stefan Willför aaÅbo Akademi Process Chemistry Center,c/o Laboratory of Wood and Paper Chemistry,Porthansgatan 3,FI-20500Åbo Turku,FinlandbÅbo Akademi Process Chemistry Center,c/o Laboratory of Industrial Chemistry and Reaction Engineering,Biskopsgatan 8,FI-20500Åbo Turku,Finland cÅbo Akademi Process Chemistry Center,c/o Laboratory of Analytical Chemistry,Biskopsgatan 8,FI-20500Åbo Turku,Finlanda r t i c l ei n f oArticle history:Received 25February 2014Received in revised form 4June 2014Accepted 23June 2014Available online 12July 2014Keywords:Hot-water extraction HemicellulosesHigh-temperature pH pH calibration Spruce wooda b s t r a c tA high-temperature pH measuring system was developed,calibrated,and validated for measuring pH during hot-water extraction of hemicelluloses from wood.The aim was to measure in-line pH during extraction in order to control the extraction pH.An yttria-stabilized Zr/ZrO 2electrode was used for measuring the potential.Phthalate and phosphate buffers were used to calibrate the system at 160,170,and 180◦C.Also,different buffer concentrations were tested for stability.Tap water and different salt solutions were tested to investigate the system response to pure water and water solutions.Calibration curves were acquired from the calibration results and Nernst equation was used to calculate the in-line pH during wood extractions.The setup showed stable and reliable potential readings during both calibration tests and wood extractions.The in-line pH was found to be 0.35pH units higher than when measured at room temperature with a conventional pH meter.©2014Elsevier B.V.All rights reserved.1.IntroductionHigh-temperature pH measurements are vastly desirable and important in several scientific and industrial fields such as geother-mal studies,water coolant circuits in nuclear reactors,plumbing,food industries,and high-temperature thermodynamic studies of aqueous solutions (Lvov et al.,1998;Manna et al.,2004;Huang et al.,2009;Jung and Yeon,2010).Biorefinery of renewable plant materials is a new emerging field where high-temperature pH mea-suring will become important.Nowadays modern biorefineries aim to utilize as much as possi-ble of a wide range of different renewable raw materials.Paper mills today use the cellulose in wood for paper production and the other wood components,mainly hemicelluloses and lignin,are often burned for energy production.Although the energy produced is vital for the process,utilizing more or even all the components in the tree for more value-added products the industry might improve the financial revenue significantly.A common method for obtaining various hemicelluloses from wood is with pressurized hot-water extraction (Song et al.,2008;Leppänen et al.,2011;Krogell et al.,2013).In recent years,studies on hot-water extraction of hemi-celluloses from wood presents an interesting additional step in∗Corresponding author.Tel.:+358400690029;fax:+35822154868.E-mail addresses:jekrogel@abo.fi,krogellj@ (J.Krogell).a biorefinery process (Yoon and van Heiningen,2008,2010;Liu,2010),where pH plays an important role.The extracted hemicel-luloses could be used as feedstock for bioethanol,biopolymers,emulsion stabilizers,and in possible health applications (Hartman et al.,2006;Ragauskas et al.,2006;Willför et al.,2008;Mikkonen et al.,2009;Xu et al.,2011).Many water properties change at higher temperature;the dielectric constant decrease,viscosity decreases,lower surface ten-sion (Yang et al.,1998),and also pH decrease.These property changes could be a reason why hot-water extraction is such a good method for hemicellulose extraction.The drop in pH during a hot-water extraction of wood is a result of a combination of the enhanced auto-ionization of water at higher temperatures,which increases the H 3O +ion concentration (Zumdahl and Zumdahl,2007)and an induced formation of acetic acid from cleaved acetyl groups from the hemicellulose chains (Liu,2010).It is a well-known fact that in acidic media,acid hydrolysis cleaves the glycosidic bonds between the sugar units in the hemicellulose chain with chain degradation and loss of molar mass as results (Lai,2001).The pH may also affect the dissolution of the hemicelluloses from the wood matrix through breaking of glycosidic bonds;however this is not yet fully proven.These examples show the importance of pH and correct in-line pH measuring and eventually in-line pH-control during extraction of hemicelluloses from wood.The conventional glass pH electrodes are not suitable for mea-surements of pH at elevated temperatures because the hydrogen/10.1016/j.indcrop.2014.06.0460926-6690/©2014Elsevier B.V.All rights reserved.10J.Krogell et al./Industrial Crops and Products61(2014)9–15ion sensitive glass membrane will degrade and loose its ion sensi-tivity(Galster,1991;Morf,1995).The upper working temperature for commercial laboratory pH electrodes are about80–100◦C, depending on if the inner reference electrolyte is in gel or liq-uid form(SI Analytics,2012).Further on,calibration of pH meters is also difficult at higher temperatures.The pH measurement is highly temperature dependent,especially at elevated temperatures (>100◦C),very little information on measured pH values for buffers at these temperatures are to be found.Some literature mention measured pH values above100◦C but they are few and originate from1960s(Le Peintre,1960;Krykov et al.,1966).Over the last decades,beginning in the early1980s,high-temperature and high-pressure compatible pH electrodes have been developed.These electrodes are mainly ceramic solid metal/metal oxide electrodes and the yttria-stabilized zirconium oxide(YS Zr/ZrO2)electrode is probably the most common (Niedrach,1980a;Niedrach and Stoddard,1985;Lvov et al.,2000, 2003).The YS Zr/ZrO2ceramic membrane is in fact an oxygen-ion conducting membrane,but because of the close relation between oxygen and hydrogen ions in the potential determining reaction O2+4H++4e−=2H2Othe electrode also functions well as a hydrogen sensitive(pH)elec-trode(Niedrach,1980a,b).Since the Zr/ZrO2electrode also is very stable regarding corrosion and redox potential at high tempera-tures it has been used as an excellent reference electrode when measuring corrosion and redox potentials in high temperature aqueous solutions(Niedrach,1982;Niedrach and Stoddard,1985).The aims of this work were to construct,calibrate,and validate the setup for a high-temperature and high-pressure pH measur-ing system,as well as evaluate the measurements for hot-water extraction of hemicelluloses from spruce wood.2.Material and methods2.1.Reactor setupThe experiments were carried out in a1000mL stainless steel 316batch reactor system(Autoclave Engineers,PA,USA)(Fig.1). The system was equipped with a Dispersimax TM turbine stirrer, heating mantle,and a sampling valve.The temperature was con-trolled by a Eurotherm2416temperature controller(Eurotherm, VA,USA)and logged to a computer with PicoLog TC datalogger and PicoLog software.Furthermore the system was equipped with a solid ZrO2-based high-temperature and high-pressure pH elec-trode(Corr Instruments,TX,USA)and a high-temperature and high-pressure Ag/AgCl reference electrode(Corr Instruments,TX, USA).The pH electrode was an yttria-stabilized Zr/ZrO2membrane electrode with a Queon TM seal and a pressure range of0–136bars and temperature range of90–305◦C.The reference electrode was a0.1N KClfilled internal pressure-balanced Ag/AgCl electrode witha ceramic frit as a junction partly based on ZrO2,Queon TM seal and a pressure range of0–136bars and temperature range of0–305◦C. The potential was recorded with a MeterLab®PHM220lab pH meter(Radiometer Analytical,Lyon,France)high-input impedance voltmeter and logged to a computer.2.2.MaterialsThree different sets of water samples were used for testing the system response for only water.Normal tap water from the labora-tory tap,ultrapure water with0.05M NaCl(Merck KGaA,Damstadt, Germany,Analysis grade),and ultrapure water with0.05M KCl (J.T.Baker®,Deventer,The Netherlands,Analysis grade).The ultra-pure water was taken from a Milli-Q Advantage A10Ultrapure Fig.1.Batch extractor setup.ADC,analog digital converter;PI,pressure indicator; TIC,temperature indicator and controller.Water purification system(Millipore Corporation,Billerica,MA, USA).Potassium hydrogen phthalate,C8H5KO4(Merck KGaA, Damstadt,Germany),Potassium dihydrogen phosphate,Na2HPO4 (VWR,Leuven,Belgium),and sodium monohydrogen phosphate, H2KPO4(J.T.Baker,Deventer,Holland)were used for the calibration solutions.All salts for calibration solution preparation were of analysis grade.The wood used in the extractions was knot-free sapwood from a healthy Norway spruce tree,felled in southern Finland.2.3.Methods2.3.1.TheoryNormally when measuring pH,a conventional laboratory pH meter,the glass electrode,is used.The pH meter measures the difference in potential caused by hydrogen ion activity in a solu-tion between a hydrogen ion sensitive electrode and a reference electrode(usually an Ag/AgCl electrode).Normally both electrodes are embedded in the pH probe along with a thermometer.In fact, the measured potential consists of several intermediate potentials within the pH meter.Such are the potential difference between the sample solution and the gel layers on the glass membrane(inside, as well as outside),the potential difference between the reference electrode and the reference electrolyte solution and the potential difference between the reference electrolyte and the sample solu-tion through a junction.These form a potential chain where all but the potential between the sample solution and the glass membrane are constant.With the measured potential and the temperature the pH meter uses Nernst equation(1)(Christian,1994).Although the high-temperature pH electrode used in this study is not glass-basedJ.Krogell et al./Industrial Crops and Products61(2014)9–1511 it has been shown that it follows Nernstian behavior and thereforeEqs.(1)and(2)can be used(Lvov et al.,2003).E=E0−2.303RTF×(−lg(˛H))(1)or rearranged Eq.(2)to calculate pH from the potentialpH=E0−ES(2)where E is the measured potential,E0is the standard electrode potential,R is the gas constant,T is the temperature in Kelvin,Fis Faradays constant,a is the activity of the measured specie,in this case the hydrogen ion and S is2.303×RT/F.S is also known as the calibration slope.The standard electrode potential,E0,is a constant that includes the different internal potentials e.g.diffusion poten-tial,different phase boundaries potential,as well as an asymmetry potential.The asymmetry potential exists across the glass mem-brane and is a result from physical defects of the membrane such as non-uniform composition,mechanical and chemical attacks,and the degree of hydration.This will slowly change with time and it is therefore very important to calibrate the pH meter from time to time(Christian,1994).2.3.2.CalibrationBecause the working range of the commercial high-temperature pH electrode used in this work is from90◦C to200◦C,it is not possible to calibrate the system with buffers at room temperature, as it is normally done with conventional laboratory pH meters. And because the potential response is very temperature depend-ent,calibration at room temperature would not be valid at higher temperatures anyway.Nernst equation(Eq.(2))is used for calculating pH values from the measured potential.To be able to do so,E0and S should be known and to determine E0and S for the system one should have solutions with known and stable pH at the used tempera-tures.Data on pH values for diluted sulfuric acid(0.0005M)and diluted sodium hydroxide(0.001M)at elevated temperatures was provided by the manufacturer and these solutions were tested at 170◦C.Unfortunately the potential responses from the electrodes were not very stable(especially for the NaOH)and,because of drifting,no good readings could be achieved.Hence buffers with different pH were tested at160◦C,170◦C,and180◦C.The different buffer solutions were0.05mol/kg potassium hydrogen phthalate with a pH of4.005at25◦C,0.025mol/kg disodium hydrogen phos-phate+0.025mol/kg potassium dihydrogen phosphate with a pH of 6.857at25◦C.These buffers gave stable mV readings at the studied temperatures.The pH values for these buffers at the high tempera-tures were taken from Galster(1991)in accordance to the electrode manufacturer.Galster reported pH values for the phthalate buffer up to150◦C so an extrapolation was made with goodfit to provide the pH values for160,170,and180◦C.The pH values for the phos-phate buffer was reported for100,125,150,175,200,225,and 250◦C so a model wasfitted to the plotted curve to get the pH val-ues at160,170,and180◦C for the phosphate buffer as well.With these acquired values,it was possible to plot the known pH val-ues against the measured potential of the phthalate and phosphate buffers at different temperatures to acquire the calibration curves.Inserting the y-axis intercept(E0)and the slope(S)from the calibration curve with the potential(E)measured during a wood extraction into Eq.(2)gives the in-line pH value during the extrac-tion.2.3.3.Wood extractionWood extractions were carried out with wood particles (1.25–2mm)of spruce sapwood with a liquid to wood ratio of33at 170◦C to test the system response.A removable protection net was20406080100120140160180200 2503003504004504321Time (h)Potentia l (m V)Temperature (°C)Temperatur ePotentialTapwater20406080100120140160180200 3253503754004321KClNaClTemperatur ePotentialTime (h)Potentia l (m V)Temperature (°C)water with saltsUltrapureFig.2.Potential response from different water tests at160,170and180◦C Tap water (top)and ultrapure water with0.05M NaCl and0.05M KCl salt addition(bottom).constructed and installed in the reactor between the electrodes and the wood material and stirrer.This was used during wood extrac-tions to prevent wood particles from damaging the electrodes and prevent particles to get stuck inside the protective tube of the elec-trodes.Samples of the extract were taken from the reactor when the temperature reached170◦C,after2.5min,5min,10min,20min, 60min,and120min.The samples were then cooled down to room temperature and pH was measured with a conventional glass elec-trode pH meter.The heating time for the system to reach170◦C was about40min.3.Results and discussion3.1.Water testsTap water,0.25M NaCl and0.25M KCl solutions of ultrapure water were tested to investigate how the electrodes respond to pure water and water solutions.Parallel experiments were made at160,170,and180◦C for each sample.The salt solutions showed by far the best stability for electrochemical potential readings with very little signal noise compared to the tap water(Fig.2).The tap water tests showed more signal noise than the salt solutions, which corroborates that ions in general,not necessarily hydrogen ions,present in the solution stabilize the system due to increased conductivity(Galster,1991).The conductivity for tap water was 218␮S/cm,and much higher for the0.25M NaCl and the0.25M KCl solutions,2.9mS/cm and3.4mS/cm,respectively.A slight shift in potential between the parallel experiments,nor-mally between0and5mV could be observed for all the different water tests.Recalculated to pH a difference of5mV corresponds to about0.08pH units at room temperature.The difference in poten-tial was also slightly increasing with a couple of mV during the experiment time for the tap water.Overall the repeatability can be considered good since the difference in mV between the experi-ments only corresponds to a difference in pH of about0.08.TheJ.Krogell et al./Industrial Crops and Products 61(2014)9–1513y = 0.00002x 2+ 0.00119x +3.96800R² = 0.999003.544.5520015010050Phthalate bufferTemperature (°C)pHy = 0.00002x 20.00194x + 6.88378-R² = 0.9963067830025020015010050Phosphate bufferTemperature (°C)pHFig.4.pH values at different temperatures for 0.05mol/kg potassium hydrogen phthalate buffer and 0.025mol/kg disodium hydrogen phosphate +0.025mol/kg potassiumdihydrogen phosphate buffer.The thick lines are values from literature (Galster,1991)while the dotted line is an extrapolation of the literature values.y = -76.01x + 950.27y = -87.89x + 986.21y = -90.09x + 992.39y = -92.29x + 1,001.4625030035040045050055060065070012108642100 °C 160 °C 170 °C 180 °CPot ent ial (mV)Estimated pHFig.5.Calibration curves for 100◦C,160◦C,170◦C,and 180◦C with the slope factor and intercept described in the line equations for the different temperatures.With the measured potential for the different buffers at the dif-ferent temperatures and the estimated pH it was possible to plot the potential versus the estimated pH (Fig.5).The plot describes lines with a slope and an intercept,which are used in Eq.(2)for calculating the in-line pH value during wood extractions at the different temperatures.Table 2presents the slopes and intercepts,as well as the potentials and estimated pH values at the different temperatures.To check how close the measured slope was to the theoretical values,a comparison between these two was made.The theoretical slope for the high temperatures was calculated as mentioned in Section 2.3.1and the results are presented in Table 3.The theoretical calibration slope is naturally a straight line,but the measured slope starts to differ from the theoretical after 100◦C.As stated earlier,not even laboratory pH meters show the theo-retical pH even at room temperature;normally a deviation of a couple of percent is acceptable (SCHOTT Instruments handylab pH 12Operation manual 2011).Therefore,the deviation of the slope for the high-temperature pH electrodes at the high temperatures is to be expected.Furthermore,as the electrodes undergo aging the potential response also changes with time.The high-temperature electrodes have also showed this behavior,approximately a dif-ference of 5mV over a 6months period.Therefore it is important to calibrate the electrodes before using them on a weekly basis as it is for conventional glass pH meters.The change in poten-tial varies depending on usage,application conditions,and storage conditions.A buffer concentration study was made to investigate what effect the buffer concentration has on the potential response.Phthalate buffer (pH 4)and phosphate buffer (pH 7)was selectedfor300350400450500550600650mol/L(mV)Potential Fig.6.Potential response for phthalate buffer and phosphate buffer solutions with different concentration at 160◦C,170◦C and 180◦C.this study with three different concentrations respectively,0.01M,0.05M and 0.1M.Fig.6shows the result from the concentration study.The results in Fig.6suggest that the potential responses are slightly lower with increased temperature for both buffers.This phenomenon can be explained from the nature of Nernst equa-tion (1);when the temperature increases on the right-hand side of the equality sign it decreases the potential on the left-hand side.The same was seen in the buffer solution experiments (Fig.3).The slight incline of the lines in Fig.6shows that the potential response is slightly lower for more diluted buffers.In terms of pH,this means that pH actually increases when a buffer is diluted.This is due to a decrease in ionic strength,which will increase the activity coef-ficient of the buffer salt leading to a slight increase in pH (Perrin and Dempsey,1974;Christian,1994).This phenomenon was also observed when the same buffers with the same concentrations were tested at room temperature with a conventional pH meter.The relative standard deviation for the buffer concentration tests were between 0.25and 3.2mV for the phthalate buffer and below 1mV for the phosphate buffer.A general trend was that the RSD decreased with increasing concentration,especially for the phos-phate buffer.The stable results from the buffer concentration study also confirm that the high-temperature electrodes were working properly and can be used in practice,i.e.for wood extractions.3.3.Wood extractionWith stable and reliable potential readings from the different buffers,it was possible to recalculate the measured potential read-ings from the wood extractions using Eq.(2)and slope and intercept14J.Krogell et al./Industrial Crops and Products 61(2014)9–153.03.54.04.55.03:303:002:302:001:301:000:300:00Time (h)Fig.7.In-line pH measurements during two 170◦C hot-water extractions of spruce wood.Solid lines represent in-line measurements and dotted lines pH measured with a conventional glass electrode at room temperature.from Table 2to actual in-line pH during wood extraction.Two par-allel wood extractions were made at 170◦C and the in-line pH of those extractions is presented in Fig.7,as well as the measured pH after sample cool down.The pH value measured in-line was about 0.35pH units higher than that measured at room temperature.A reason for this dif-ference could be that the dissociation of acetic acid,the main contributor to the pH drop during the extraction,is slightly exother-mic and p K a increases at higher temperatures (Fisher and Barnes,1972).The equilibrium is therefore shifted toward the protonated form of the acid,with less free hydrogen ions in the solution.When the samples cool down to ambient temperatures,the pH thus decreases.Previous studies of hot-water extraction of hemicellu-loses from spruce show the same pH profile and also a significant depolymerization of the hemicelluloses when the pH decreases (Song et al.,2008,2011;Krogell et al.,2013).At pH 4and below,the average molar mass decreased substantially already after 10min of extraction.These new findings in our study suggest that the hydrol-ysis of hemicellulose chains takes place already at significantly higher pH at these elevated temperatures.With a potential RSD 0.5mV that corresponds to a pH RSD of 0.01units between the parallel wood extractions show yet again good repeatability and stability and more important,the pH measured in-line follows in parallel with the pH measured with a laboratory pH meter after the samples cooled down.This gives an indication that the in-line pH system is working and the calculation theory is correct.This will have a positive impact on the possibility to measure and adjust the pH in hot-water extractions of a particular plant biomass and thus to control the extraction and subsequent degradation of polymeric substances.4.ConclusionsRepeatable and reliable high-temperature pH measurements can be made during hot-water extraction of hemicelluloses from wood with an yttria stabilized Zr/ZrO 2pH electrode after calibra-tion with phthalate and phosphate buffers.The in-line pH at 170◦C was shown to be about 0.35units higher than when samples had been cooled down to room temperature and measured with at con-ventional pH meter.The in-line pH measurement possible it opens up for the possibility of continuous in-line pH control during extrac-tion process and with that a better opportunity to tailor the end products.AcknowledgementsThe authors would like to thank Lietai Yang,Ph.D.at Corr Instruments for the help with the many questions about the elec-trodes and Jimmy Dahlqvist at the Åbo Akademi University metalworkshop for manufacturing of the custom made protective net for the electrodes.This work is part of the activities at the Åbo Akademi University Process Chemistry Center.Financial support from FuBio Joint Research 2is gratefully acknowledged,as well as support from the Doctoral Program for Biomass Refining (BIOREGS)and European Polysaccharide Network of Excellence (EPNOE).ReferencesChristian,G.D.,1994.Potentiometry.Analytical Chemistry,191.,5th ed.John Wiley&Sons,Inc.,New York,pp.299–345.Fisher,J.R.,Barnes,H.L.,1972.The ion-product constant of water to 350◦C.J.Phys.Chem.76,90–99.Galster,H.,1991.pH measurement Fundamentals,Methods,Applications,Instru-mentations.VCH Verlagsgesellschaft,Weinheim,pp.60,168,262.Hartman,J.,Albertsson,A.-C.,Söderqvist Lindblad,M.,Sjöberg,J.,2006.Oxygenbarrier materials from renewable sources:material properties of softwood hemicellulose-based films.J.Appl.Polym.Sci.100,2985–2991.Huang,J.,Wu,X.,Han,E.-H.,2009.Influence of pH on 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最新大气复习资料含答案

最新大气复习资料含答案

大气复习资料含答案大气复习资料一、概念解释(1)Globe warming:Global warming is the increase in the average measured temperature of the Earth's near-surfaceair and oceans since the mid-twentieth century, and itsprojected continuation.(2) Temperature inversions:A temperature inversions is a thin layer of the atmosphere where the decrease in temperaturewith height is much less than normal (or in extreme cases,the temperature increases with height).(3)ESP: Electrostatic precipitator, which is like a gravity setter or centrifugal separator, but electrostatic forcedrives the particles to the wall.(4)HEPA: High Efficiency Particulate Air(5)Lean bum :Lean burn refers to the use of lean mixtures in an internal combustion engine .The air-fuel can be as highas 65:1 ,so the mixture has considerably less fuel incomparison to the stoichiometric combustion ratio (14.7 forpetrol , for example ).(6)Plume rise: the plume rising a distance △h above the top of the stack before leveling out.(7)Wet scrubber: A device that collects particles by contacting the dirty gas stream with liquid drops.(8) Photochemical smog:(9)Thermal NO: Thermal NO x refers to NO x formed through high temperature oxidation of the diatomic nitrogen found incombustion air.(10)A/F ratio: Air to fuel ratio for auto engines.(11)PM2.5:particle with the aerodynamic diameter less than2.5 um, which is also called Respirable Particles.(12)Alternative fuel: Several other fuels except of conventional gasoline and diesel, which have been used formany years in slighutly modified automobile engines, forreasons of cost and availability.(13)VOCs: Volatile organic compounds are those organic liquids or solids whose room temperature vapor pressure aregreater than about 0.01 psia(=0.0007atm) and whoseatmospheric boiling points are up to about 500℉, whichmeans most organic compounds with less than 12 carbon atoms.(1)SCR and SNCR:6NO+4NH3→5N2+6H2O, 4NO+4NH3+O2→4N2+6H2O2NO2+4NH3→3N2+6H2O.These reactions can be carried out over a variety of catalysts, the temperature is between 1600℉and 1800℉, once the temperature increases, the dominant reaction isNH3+O2→NO+1.5H2O, the catalytic processes are called SCR,and the higher-temperature ones, without catalysts, callSNCR.(2)Aerodynamic diameter: Airborne particles have irregular shapes, and their aerodynamic behavior is expressed interms of the diameter of an idealized spherical particleknown as Aerodynamic diameter.(3)Primary Particles: Particles found in the atmosphere in the form in which they were emitted, for examples, NO,CO,SO2(4)Point Sources: small number of large sources that emit larger amounts per source, at higher elevations (powerplants, smelters, cement plants, etc.) called point sources 二、Answer following questions(1)Which are the main constituents for the ground level ozone formation?Ozone is formed when the following constituents are present. Nitrogen oxides, Volatile Organic, Compounds, Sunlight, High temperature(>18 ℃)NO+VOC+O2+Sunlight→NO2+O3(2)Please list five major types of wet scrubbers.Plate Scrubber (板式)Packed Scrubber (填料式)Preformed Spray Scrubber(喷雾式)Gas-Atomized Spray Scrubber (气体雾化)Centrifugal Scrubber (离心式)Impingement-Entrainment Scrubber(冲击夹带式)Mechanically Aided Scrubber (机械辅助式)Moving Bed Scrubber (移动床式)(3)How to control VOCs pollution by prevention? Two examples. Substitution(代替),Replacing gasoline as a motor fuel with compressed natural gas or propane is a form of substitution. Process Modification(过程修改),Replacing gasoline-powered vehicles with electric-powered vehicles is a form of process modification.Leakage(渗漏)Control,Storing large amounts of gasoline in floating roof tanks.(4)Please introduce the process of forced-oxidation LimestoneWetScrubbing briefly?(5)What are the most different points between SCR and SNCR?(6)Can TWC be applied in the treatment of diesel exhaust(=emissionof diesel engine)? Why?·The characteristic of emission of diesel engine: Ample PM and Excessive O2, Lower temperature;·The difficulty in the reaction of solid-gas-solid.Key: The mixture process of fuel and air for gas engines is distinguished from that for diesel engines, hence the character of one type engine is different from the other one: there are mainlyfive gases (NOX , HC, CO and O2, CO2) in the exhaust of gas motors,while there are ample O2and four other gases mentioned above in thetailpipe emission of diesel engine. And the presence of abundant O2 would inhibit the performance of TWC.Moreover, the contact and reaction of solid-solid-gas resulting in the difficulties for catalysts to oxidation the particulate in the exhaust of diesel engine, while the contact and reaction of solid-gas-gas occur in the exhaust of gasoline engine and the latter reaction is easier.(7)What kinds of indoor air pollutants are mostly concernedbypublic?a)Randomb)Combustion by-products1.CO, CO2, SO2,Formaldehyde,Hydrocarbons,NOx2.Particulates, polyaromatic hydrocarbonsc)Cigarettes d)Volatile organic compoundsf) Biological contaminants(8)List the technology strategy for the control of particles.(9)Give names of three typical kinds of combustion reactors.Whichhas lowest operator temperature among those reactors?1.Direct flame incineration2.Thermal incineration3.Catalytic incineration (has lowest operator temperature)(10)What are the major development problems of Forced-oxidation limestone wet scrubbing?(11)What are primary air pollutants and secondary airpollutants?Any example?primary air pollutants are directly from the sources, for examples, NO, CO, SO2.The secondary air pollutants are from the primary pollutants, such as NO2, NO3, fine particles.NO+CH+O2+sunlight → NO2+O3 (12)Basic strategy of control for particulate pollutants(threeaspects )?Impaction 碰撞 Interception 截留 Diffusion 扩散By forcing the individual particles to contact each other,By contacting them with drops of water,By preventing the emission of gaseous Pollutants.(13)How to reduce the formation of NOx in flue gas bymodifying the combustion processes?p459(14)Please explain the formation of acid rain?Sulfur oxides and nitrogen oxidesNO NO2 HNO3nitric acid SO2H2SO4sulfuric acid(15)What are basic principles of electrostatic Precipitators(sixactivities)?·Ionization - Charging of particles·Migration - Transporting the charged particles to the collecting surfaces·Collection - Precipitation of the charged particles onto thecollecting surfaces·Charge dissipation - Neutralizing the charged particles on the collecting surfaces·Particle dislodging - Removing the particles from the collecting surface to the hopper·Particle removal - Conveying the particles from the hopper to a disposal point三、Calculation1) Estimate the concentration of carbon monoxide at the downwind edge of a city. The city may be considered to consist of three parallel strips, located perpendicular to the wind. For all of the strips the wind velocity u equals 3 m/s . The properties of each of the strips are described in the following table,solution :uHb c += c 1=0+(100*5000)/(3*400)=416.7 μg/m 3 uHqL c +=1C c 2=416.7+(500*2000)/(3*500)=1083.4μg/m 3 uHqL c +=2C c 3=1083.4+(100*5000)/(3*400)=1500.1μg/m 32) An ESP is designed to treat 540,000 acfm (actual cubic feet per minute ) with 99% efficiency . Assuming an effective drift velocity of 0.12 m/s , calculate therequired plate area and the number of plates. The plate size is 5.4m tall by 3m long (A =-Q×㏑(1-η)/ωp , acfm =1ft 3/min, 1m=3.28ft, 1m 2=1550 in 2=10.7639 ft 2).solution1ft 3/min=(1/3.28)3m 3/min=0.0283 m 3/min540000acfm=540000*0.028315282 m 3/min=254.7 m 3/sA= -(254.7/0.12)ln(1-0.99)=9774.47m 2N=9774.47/514.3=6043) We wish to treat an airstream containing 0.005mol fraction (0.5%, 5000ppm )toluene, moving at a flow rate 2240m 3/h at 0℃ and 1 atm , so as to remove 99% of the toluene by water absorption. Estimate the required water flow rate. Here Henry’s law constant is 10000 atm .Solution :4)A power plant flue gas contains 1000ppm of SO 2 and is emitted at a rate of 224m 3/s at 546K and 1 atm . A Forced-oxidation limestone wet scrubbing system is to be used to achieve 90% removal of the SO 2. Calculate the amount of CaSO 4·2H 2O contained in the final solid product in t/d.Solution : RTPV n = =(101325*224*1000*10-6)/(8.315*546)=4.999mol/s SO 2~ CaSO 4·2H 2O so n (c a so 4)=n (so 2)=4.999mol/s*90%=4.4991mol/sm=4.4991mol/s *172g/mol *3600*24s/d *10-6 t/d=66.86 t/d5)A power plant emits 36 kg/h of SO 2 at height H=120m and the wind speed is 2 m/s. Dispersion Coefficients: σy =40m and σz =30m, Estimate the ground-level concentration of SO 2 from this source at a distance 1km directly downwind?()⎪⎭⎪⎬⎫⎪⎩⎪⎨⎧⎥⎥⎦⎤⎢⎢⎣⎡⎥⎦⎤⎢⎣⎡+-+⎥⎥⎦⎤⎢⎢⎣⎡⎥⎦⎤⎢⎣⎡--⎥⎥⎦⎤⎢⎢⎣⎡⎥⎥⎦⎤⎢⎢⎣⎡-=22221exp 21exp 21exp 2,,z z y z y H z H z y u Q z y x C σσσπσσ Solution :u=2m/s , H=120m, Q=36kg/h=10g/s , y=0 , z=H=120 , x=1000m⎭⎬⎫⎩⎨⎧+⎥⎦⎤⎢⎣⎡⎥⎦⎤⎢⎣⎡+-=130********exp 30*40*3.14*10*210C =0.406)A power plant flue gas contains 1000×10-6 (1000ppm )of NOx ,and isemitted at a rate of 89.6m3/s at 546K and 1 atm. The NOx is 90%mol NO, balance NO2. A selective catalytic reduction system is to be used to remove the NOx. Calculate the minimum of ammonia needed in kg/h.Solution: 4NO+4NH3+O2→4N2+6H2O 2O+4NH3+O2→3N2+6H2OPV=nRT n=(101325*89.6*1000*10-6)/(8.315*546)=2.0mol/sn(no)=0.9*2mol/s=1.8mol/s so n(no2)=2.0-1.8=0.2mol/sn(NH3)= n(no)+2* n(no2)=1.8+0.4=2.2mol/sm=2.2mol/s * 17 g/mol =37.4g/s=134.64kg/h7)The efficiency of an ESP is 98%. The efficiency of the ESP drops to 93% as a result of flow rate changes. Calculate the ratio of flow rates for the above situation. Use appropriate assumptionSolution: A =-Q×㏑(1-η)/ωp SO Q=-A*ωp/㏑(1-η)Assume the plate area A and the effective drive velocity ωp are unchanged.ThenQ1/Q2=(-A1*ωp/㏑(1-η1)/ (-A2*ωp/㏑(1-η2)=㏑(1-η2)/ ㏑(1-η1)=㏑(1-0.93)/ ㏑(1-0.98)=0.68。

2024年高一英语气候科学研究进展练习题40题

2024年高一英语气候科学研究进展练习题40题

2024年高一英语气候科学研究进展练习题40题1.Climate change is mainly caused by the increase in _____.A.greenhouse gasesB.pollutionC.wasteD.noise答案:A。

“greenhouse gases”是温室气体,气候变化主要是由温室气体增加引起的。

“pollution”污染,范围太广,不一定直接导致气候变化。

“waste”废物,和气候变化关系不大。

“noise”噪音,与气候变化毫无关系。

2.Scientists are studying ways to reduce _____.A.climate changeB.global warmingC.pollution levelsD.carbon emissions答案:D。

“carbon emissions”是碳排放,科学家正在研究减少碳排放的方法。

“climate change”气候变化是结果不是要减少的对象。

“global warming”全球变暖也是结果。

“pollution levels”污染水平,比较宽泛,不如减少碳排放具体针对气候变化。

3.The melting of glaciers is a result of _____.A.rising temperaturesB.polluted airC.waste disposalD.noise pollution答案:A。

冰川融化是温度上升的结果。

“polluted air”污染的空气,不是冰川融化的直接原因。

“waste disposal”废物处理,与冰川融化无关。

“noise pollution”噪音污染,和冰川融化毫无关系。

4.One way to combat climate change is to increase the use of _____.A.fossil fuelsB.renewable energyC.nuclear powerD.coal答案:B。

蒸汽和热量计算机说明书

蒸汽和热量计算机说明书

Steam and Heat Computer for Industrial Energy Calculation of Steam and WaterApplication •Energy management •Chemical industry•Heating and air conditioning •Pharmaceutical industry •Food and beverage•Plant and panel manufactureYour benefits•Calculation of the following applications:Steam mass, steam heat quantity, net steam quantity, steam-heat differential,water heat quantity, waterheat differential•Simultaneous calculation of up to three applications per device •Real time clock•Log book function for error messages and parameter changes with date and time •Presettable allocation of the inputs/outputs to each application•Configuration and operation using a serial interface and ReadWin 2000 PC software•Modular expansion using plug-in cards•Large back-lit LC display with color change in the event of an error•Quick and safe configuration with application-guided operation (Quick Setup)•Online help function on all parameters optional •Calculation as per IAPWS-IF 97•Meets standards EN 1434-1, 2, 5 and 6 and OIML R75•Bi-directional flow applications or energy measurement is possible •Split-range flow measurements •Averaging of several input signals•Flow compensation due to improved differential pressure procedure •UL recognized component to UL 3111-1Products Solutions ServicesTechnical Information RMS621Energy managerTI00092R/09/EN/14.1671355039RMS6212Endress+HauserFunction and system designMeasuring principleUp to three different applications per device can be processed simultaneously. Two separate counters are available for each application, each of them is resettable.Connection of measured variables 0/4 to 20 mA, PFM or pulse for sensors such as flow (differential pressure probes, vortex, turbine, orifice plate, among others) or pressure. When measuringtemperatures, Pt100, Pt500 and Pt1000 in a 3- or 4-wire system can be connected directly or as a 4 to 20 mA signal using temperature transmitters (e.g. TMT181). A separate transmitter power supply is installed for each analog or pulse input. The available outputs are signal types 0/4 to 20 mA, pulse, digital and relay. The number of inputs, outputs, relays and transmitter powersupplies contained in the basic device can be individually extended over a maximum of three plug-in cards.In applications with overheated steam, the process is monitored for saturated steam or wet steam. If the saturated steam curve is reached, this can be output as an alarm value. The summation of the calculated values is not interrupted when process limits (e.g. saturated steam curve) are exceeded or below set values. The most recently valid values are registered in the event memory when they leave or return to the valid process limits.ApplicationsSteam massCalculation of the mass flow in a steam line from the process variables for flow, pressure and temperature. In saturated steam operation, the mass flow is calculated from two input variables (pressurecompensated or temperature-compensated).Steam heat quantityCalculation of the mass flow and its quantity of heat (energy) in a steam line from the processvariables for flow, pressure and temperature. Saturated steam operation is possible, calculation is the same as for steam mass.p 1Calculation of the steam mass flow and steam heat quantity from the input variables for flow (Q), pressure (p) and temperature (T)Steam - heat - differentialCalculation of the quantity of heat emitted or absorbed in a steam application using temperature differential measurement from the process variables for flow, pressure and two temperature values.Balancing a steam generation process (phase transition: water → steam) or a steam heating process (phase transition: steam → water) is steam quantityCalculation of the quantity of heat that can be extracted from a steam mass flow until it condenses to water. Process variables: flow, pressure, temperature. For saturated steam, the calculation is made from two input variables.RMS621Endress+Hauser 3p 2Calculation of the steam-heat differential and net steam quantity from the input variables for flow(Q),pressure (p) and the temperature differential (T1 - T2)Water heat quantityCalculation of the quantity of heat in a water flow from the process variables for flow and temperature.Water-heat differentialCalculation of the quantity of heat that is emitted or absorbed by a water flow in a heating or cooling system. The quantity of heat is calculated from the process variable for flow and the differential from the feed and return temperature. Bidirectional energy calculations, such as the calculating systemswith changing flow direction (charging/discharging the heat accumulator) are also possible.3Calculation of the water heat quantity and water-heat differential from the input variables for flow (Q)and the temperature differential (T1 - T2)Measuring systemThe analog input variables are digitized, the pulse and PFM signals recorded using period length/frequency measurement and processed further in the arithmetic unit controlled by themicrocontroller. The energy values are calculated in accordance with the highly precise equations of the international industry standard IAPWS-IF97, which makes the calculation quicker and more precise. This guarantees maximum precision and high calculating speed in all temperature ranges.The internal real time clock with power reserve is used to integrate the flow values. Both the input variables and the results can be transferred via the outputs.When a differential pressure signal is used, the sensor data is recalculated over the entire working range of the flow sensors.Configuration of the inputs, outputs, alarm values, the display as well as commissioning andmaintenance of the device can be performed via 8 soft keys with the back-lit dot matrix display, or using the RS232 interface with the ReadWin 2000 PC software or using an external display and operating unit.RMS6214Endress+HauserA menu-guided quick setup is available on request for the initial start-up. Online help makes on-site operation easier. The color change of the background lighting visualizes alarm value violations or faults. A function expansion of the device by means of expansion cards can be made at any time.Arithmetic unitRMS621Endress+Hauser 5InputMeasured variable Current, PFM, pulse, temperatureInput signal Flow, differential pressure, pressure, temperatureNumber:•2 x 0/4 to 20 mA/PFM/pulse•2 x Pt100/500/1000 (in basic device)Maximum number:10 (depends on the number and type of expansion cards)Galvanic isolationThe inputs are galvanically isolated between the individual expansion cards and the basic device (see also ’Galvanic isolation’ under Output).RMS6216Endress+HauserOuputOutput signal Current, pulse, transmitter power supply (TPS) and switching output Galvanic isolationBasic device:The specified insulation voltage is the AC testing voltage U eff , which is applied between the connections.Basis for assessment: IEC 61010-1 (EN 61010-1), protection class II, overvoltage category II.Current - pulse output variableCurrent •0/4 to 20 mA +10% overrange, invertible•maximum loop current 22 mA (short-circuit current)•Load maximum 750 Ω at 20 mA •Accuracy 0.1% of full scale value•Temperature drift: 0.1% / 10 K (18 °F) ambient temperature change •Output Ripple < 10 mV at 500 Ω for frequencies < 50 kHz •Resolution 13 Bit•Error signals 3.6 mA and 21 mA limits as per NAMUR NE43 adjustablePulseBasic device:•Frequency range to 2 kHz•Voltage level 0 to 1 V low, 24 V high ±15%•Load minimum 1 kΩ•Pulse width 0.25 to 1 000 msExpansion cards (digital passive, open collector):•Frequency range to 2 kHz •I max = 200 mA •U max = 24 V ±15%•U low/max = 1.3 V bei 200 mA •Pulse width 0.25 to 1 000 ms NumberNumber:2 x 0/4 to 20 mA/pulse (in basic device)RMS621Endress+Hauser 7maximum number•8 x 0/4 to 20 mA/pulse (depends on the number of expansion cards)•6 x digital passive (depends on the number of expansion cards)Signal sourcesAll available multifunctional inputs (current, PFM or pulse inputs) and results can be freely allocated to the outputs.Switching outputFunctionLimit relay switches in these operating modes: minimum, maximum safety, gradient, alarm,saturated steam alarm, frequency/pulse, device error Switch behaviorBinary, switches when the alarm value is reached (potential-free NO contact)Relay switching capacitymaximum 250 V AC , 3 A / 30 V DC, 3 AWhen using relays on expansion cards, a mixture of low voltage and extra-low voltage is not permitted.Switching frequency maximum 5 Hz Switching thresholdProgrammable (wet steam alarm is preset at 2 °C (3.6 °F) at the factory)Hysteresis 0 to 99%Signal sourceAll available inputs and calculated variables can be allocated freely to the switching outputs.Number•1 (in basic device)•Maximum number: 7 (depends on the number and type of expansion cards)Number of output states 100 000Scan rate 500 msTransmitter power supply and external power supply•Transmitter power supply unit, terminals 81/82 or 81/83 (optional universal expansion cards 181/182 or 181/183):–Maximum supply voltage 24 V DC ±15%–Impedance < 345 Ω–Maximum output current 22 mA (for U out > 16 V)–HART® communication is not impaired –Number: 2 (in basic device)–maximum number: 5 (depending on the number and type of expansion cards)•Additional power supply (e.g. external display), terminals 91/92:–Supply voltage 24 V DC ±5%–Maximum current 80 mA, short-circuit proof –Number: 1–Source resistance < 10 ΩRMS6218Endress+HauserPower supply4Power supply; 90 to 250 V AC 50/60 Hz, 20 to 36 V DC , 20 to 28 V AC 50/60 HzThe terminals are bridged internally and can be used as support points for series wiring.5PFM, current and pulse inputs of the energy managerRMS621Endress+Hauser9 6Temperature inputs of the energy manager; terminals 1, 2, 5, 6: input 1; terminals 3, 4, 7, 8: input 2*Optional: Terminal assignment temperature expansion cardThe terminals 1 and 5 or 3 and 7 respectively must be bridged for 3-wire connection.7Outputs of the energy managers1Relay 1; terminal 142, 143 (relay 1) and 152, 153 (relay 2) as an option in expansion card2Pulse and current outputs3Pulse outputs (Open Collector) as an option in expansion card8Transmitter power supplyRMS62110Endress+Hauser 9Interfaces RS48510Connection of remote display and operating unit (option)1Energy manager2Display and operating unitSupply voltage•Low voltage power unit: 90 to 250 V AC 50/60 Hz•Extra-low voltage power unit: 20 to 36 V DC, 20 to 28 V AC 50/60 HzPower consumption8 to 26 VA (in Abhängigkeit der Ausbaustufe)Connection data interface RS232•Connection: 3.5 mm jack plug on front panel•Transmission protocol: ReadWin 2000•Transmission rate: maximum 57600 BaudRS485•Connection: plug-in terminals 101/102 (in basic device)•Transmission protocol: (serial: ReadWin 2000; parallel: open standard)•Transmission rate: maximum 57600 BaudOptional: additional RS485 interface•Connection: plug-in terminals 103/104•Transmission protocol and transmission rate same as standard RS485 interfaceRMS621Endress+Hauser 11Performance characteristicsReference operating conditions •Power supply 230 V AC ±10%; 50 Hz ±0.5 Hz •Warm-up period > 30 min •Ambient temperature range 25 °C (77 °F) ±5 K (±9 °F)•Air humidity 39% ± 10% relative humidityMaximum measured error •Current: 0.1% of full scale value •PFM: 0.01% of full scale value •Temperature (4-wire connection):–Pt100: 0.03% of full scale value –Pt500: 0.1% of full scale value –Pt1000: 0.08% of full scale valueResolution •Current: 13 Bit •Temperature: 16 BitInfluence of ambient temperature•Current: 0.4% / 10 K (18 °F) ambient temperature change •PFM: 0.1% / 10 K (18 °F) ambient temperature change •Temperature: 0.01%/ 10 K (18 °F) ambient temperature change InstallationMounting location In the cabinet on DIN rail according to IEC 60715 TH 35Device overheating when using expansion cards ‣When using extension cards, venting with an air current of at least 0.5 m/s is necessary.Orientation No restrictions.RMS62112Endress+HauserEnvironmentAmbient temperature range –20 to 60 °C (–4 to 140 °F)Storage temperature –30 to 70 °C (–22 to 158 °F)Climate class As per IEC 60 654-1 Class B2 / EN 1434 Klasse ’C’ (no condensation permitted)Electrical safetyAs per IEC 61010-1: ambient < 2 000 m (6 560 ft) above sea level Degree of protection •Basic device: IP 20•External display: IP 65Electromagnetic compatibility•Interference emission:IEC 61326 Class A •Interference immunity:–Power failure: 20 ms, no influence –Starting current limitation: I max /I n ≤ 50% (T50% ≤ 50 ms)–Electromagnetic fields: 10 V/m as per IEC 61000-4-3–Conducted HF: 0.15 to 80 MHz, 10 V as per IEC 61000-4-3–Electrostatic discharge: 6 000 V contact, indirect as per IEC 61000-4-2–Burst (power supply): 2 000 V as per IEC 61000-4-4–Burst (signal): 1 000 V/2 000 V as per IEC 61000-4-4–Surge (AC power supply): 1 000 V/2 000 V as per IEC 61000-4-5–Surge (DC power supply): 1 000 V/2 000 V as per IEC 61000-4-5–Surge (signal): 500 V/1 000 V as per IEC 61000-4-5RMS621Endress+Hauser 13Mechanical construction11Housing for DIN rail as per IEC 60751 TH35; dimensions in mm (in) 12Display and operating unit for panel mounting (available as an option or as an accessory); dimensions in mm (in)A B C D EA0032351 13Unit upgrade with expansion cards (optional or available as accessories)A, E Slots A and E equipped in the basic deviceB, C,DSlots B, C and D can be upgraded with expansion cardsWeight •Basic device: 500 g (17.6 oz) (in maximum configuration with expansion cards)•Remote control unit: 300 g (10.6 oz)RMS62114Endress+HauserMaterial Housing: polycarbonate plastic, UL 94V0Terminals Coded, pluggable screw terminals; Clamping area 1.5 mm 2 (16 AWG) solid, 1.0 mm 2 (18 AWG)flexible with wire end ferrule (applies to all connections).OperabilityOperating concept •Display (optional):160 x 80 Dot-matrix LCD with blue background lighting Color changes to red in the event of an error (adjustable)•LED status display:Operation: 1 x green Fault message: 1 x red •External display and operating unit (optional or as accessory):A display and operating unit can also be connected to the energy manager in the panel mounted housing, dimensions (WxHxT) 144 (5.67) x 72 (2.83) x 43 (1.69) mm (in))The connection to the integrated RS485 interface is made using the connecting cable (l = 3 m (9.84 ft)) which is included in the accessories set. Parallel operation of the external display unit with a device-internal displayin the RMS621 is possible.14External display and operating unit in the panel mounted housingOperating elements Eight front-panel soft keys interact with the display (function of the keys is shown in the display).Remote operation RS232 interface (3.5 mm (0.14 in)): jack plug on front panel): configuration via PC operating software.Real time clock •Deviation: 2.6 min per year •Power reserve: 14 daysMathematical functions•Flow, difference pressure calculation: EN ISO 5167•Continuous calculation of mass, density, enthalpy, heat quantity using stored algorithms and tables •Water / steam calculation as per IAPWS-IF97RMS621Endress+Hauser 15Certificates and approvalsCE mark The measuring system meets the legal requirements of the applicable EC guidelines. These are listed in the corresponding EC Declaration of Conformity together with the standards applied. The manufacturer confirms successful testing of the device by affixing to it the CE mark.UL approval UL recognized componentEAC mark The product meets the legal requirements of the EEU guidelines. The manufacturer confirms the successful testing of the product by affixing the EAC mark.Other standards and guidelines•IEC 60529:Degrees of protection by housing (IP code)•IEC 61010-1:Safety requirements for electrical measurement, control and laboratory instrumentation.•IEC 61326-Serie:Electromagnetic compatibility (EMC requirements).•NAMUR NE21, NE43:Standardization association for measurement and control in chemical and pharmaceutical industries ().•IAPWS-IF 97:International applicable and recognized calculation standard (since 1997) for steam and water.Issued by the International Association for the Properties of Water and Steam (IAPWS).•OIML R75:International construction regulation and test specification for water energy managers from the Organisation Internationale de Métrologie Légale.•EN 1434 1, 2, 5 und 6•EN ISO 5167:Flow measurement of fluids with throttle devices.Ordering informationDetailed ordering information is available from the following sources:•In the Product Configurator on the Endress+Hauser website: -> Click "Corporate"-> Select your country -> Click "Products" -> Select the product using the filters and search field ->Open product page -> The "Configure" button to the right of the product image opens the Product Configurator.•From your Endress+Hauser Sales Center:Product Configurator - the tool for individual product configuration •Up-to-the-minute configuration data •Depending on the device: Direct input of measuring point-specific information such as measuring range or operating language •Automatic verification of exclusion criteria •Automatic creation of the order code and its breakdown in PDF or Excel output format •Ability to order directly in the Endress+Hauser Online ShopRMS62116Endress+HauserApplication packagesThe following table contains an overview of the order codes for the expansion cards with the possible applications.RMS621Endress+Hauser 17AccessoriesVarious accessories, which can be ordered with the device or subsequently from Endress+Hauser, are available for the device. Detailed information on the order code in question is available from your local Endress+Hauser sales center or on the product page of the Endress+Hauser website: .Device-specific accessories •Display and operating unit (optional or as an accessory):Remote display for panel mounting (dimensions (WxHxD) 144 (5.67) x 72 (2.83) x 43 (1.69) mm (in))•IP 66 protective housing for field mounting DIN rail instrumentationExpansion cards A function expansion of the device by means of max. 3 extension cards (universal and/or temperature cards) is possible.•Extension card temperature Inputs: 2 x Pt100/500/1000Outputs: 2 x 0/4 to 20 mA/pulse, 2 x digital, 2 x relay •Extension card universal Inputs: 2 x 0/4 to 20 mA/PFM/pulse with TPS Outputs: 2 x 0/4 to 20 mA/pulse, 2 x digital, 2 x relay •PC configuration software ReadWin 2000 and serial configuration cable with jack plug 3.5 mm (0.14 in).Communication-specific accessories PROFIBUS interfaceDocumentation•System components and data managers - Solutions for the loop: FA00016K/09•Operating instructions RMS621: BA00255R/09/。

A note on the high temperature expansion of the density matrix for the isotropic Heisenberg

A note on the high temperature expansion of the density matrix for the isotropic Heisenberg

a r X i v :c o n d -m a t /0611454v 1 [c o n d -m a t .s t a t -m e c h ] 17 N o v 2006A note on the high temperature expansion of the density matrix for the isotropic HeisenbergchainZengo Tsuboi ∗Okayama Institute for Quantum Physics †,Kyoyama 1-9-1,Okayama 700-0015,JapanAbstractG¨o hmann,Kl¨u mper and Seel derived the multiple integral formula of the density matrix of the XXZ Heisenberg chain at finite tem-peratures.We have applied the high temperature expansion (HTE)method to isotropic case of their formula in a finite magnetic field and obtained coefficients for several short-range correlation functions.For example,we have succeeded to obtain the coefficients of the HTE ofthe 3rd neighbor correlation function <σz j σz j +3>for zero magneticfield up to the order of 25.These results expand our previous re-sults on the emptiness formation probability [Z.Tsuboi,M.Shiroishi,J.Phys.A:Math.Gen.38(2005)L363]to more general correlation functions.MSC:82B23;45G15;82B20;82B80PACS:75.10.Jm,02.30.Ik,05.70.-a,05.30.-dKey words:correlation function;density matrix;high temperature expan-sion;nonlinear integral equation;quantum transfer matrix Report-no:OIQP-06-10to appear in Physica A1IntroductionG¨o hmann,Kl¨u mper and Seel derived [1](see also [2,3,4,5])a multiple integral formula of matrix elements of a density matrix of a finite segmenttsuboi@pref.okayama.jp†URL:http://www.pref.okayama.jp/kikaku/kouryoushi/english/kouryoushi.htm1of arbitrary length m of the anti-ferromagnetic spin1/2XXZ Heisenberg infinite chain atfinite temperature in afinite magneticfield by combining the quantum transfer matrix approach[6]-[10]and the algebraic Bethe ansatz technique.Their formula generalizes the multiple integral formulae for zero temperature[11,12,13]tofinite temperature case.This is a fundamental quantity since thermal average of any operators acting non-trivially on the segment of length m can be expressed in terms of their formula.Thus it is an important problem to perform this multiple integral and extract concrete numbers from it.Their formula contains an auxiliary function,which is a solution of a nonlinear integral equation.This nonlinear integral equation is essentially same as the one for the free energy[8,9].Thus to evaluate their formula consists of two non-trivial tasks:to solve the nonlinear integral equation and to integrate the multiple integrals.In our previous paper[14], we applied the high temperature expansion(HTE)method to a multiple integral formula[3]of the emptiness formation probability P(m)for the XXX model,which is the probability of m adjacent spins being aligned upward,and succeeded to obtain the coefficients of P(3)up to the order of 42.As for zero magneticfield case,there is also numerical calculation[15] for the multiple integral for m=2,3.The purpose of this paper is to expand our previous results on the HTE for P(m)[14]to more general correlation functions for the spin1/2isotropic Heisenberg chain in a magneticfield h.In section2,we introduce the multiple integral formula of the matrix elements of the density matrix[1].In section3,we evaluate this multiple integral by the HTE method.Based on the result of the HTE of the density matrix,we will calculate the HTE of two point correlation functions(3.1)-(3.3).In particular for zero magneticfield case,we have succeeded to obtain the coefficients of the HTE of a3rd neighbor correlation function up to the order of25(cf.eq.(3.10)).Section4is devoted to concluding remarks.2Integral representation of the density ma-trixThe Hamiltonian of the spin-1/2isotropic Heisenberg chain in a magnetic field h is given asH=JLj=1(σx jσx j+1+σy jσy j+1+σz jσz j+1)−hσk j+L=σk j is assumed.Let us introduce2×2matrices:e11= 1000 ,e21= 0100 ,e12= 0010 ,e22= 0001 (2.2)These matrices are embedded into the space(C2)⊗L on which the Hamilto-nian(2.1)acts:e jαβ=I⊗(j−1)⊗eαβ⊗I⊗(L−j),(2.3) where I=e11+e22,α,β∈{1,2}and j∈{1,2,...,L}.The above Paulimatrices can be written in terms of these matrices:σx j=e j12+e j21,σy j=ie j12−ie j21,σz j=e j11−e j22.We also putσ+j=e j21andσ−j=e j12.G¨o hmann,Kl¨u mper and Seel derived[1]an integral representation of the density matrix of the XXZ chain atfinite temperature T.The isotropic (XXX)limit of their formula is given as follows.<e1α1β1e2α2β2···e mαmβm>=limL→∞T re1α1β1e2α2β2···e mαmβme−HT re−H2π(1+a(y j))(y j−i)eα+j−1y m−eα+jj ×mj=|α+|+1 C dy j a(y j))(y j+i)eβ−j−1y m−eβ−j j×det1≤j,k≤m ∂(k−1)ξG(y j,ξ)|ξ=01≤j<k≤m(y j−y k−i),(2.4)where a(v)and G(v,ξ)are solutions of the following integral equations.log a(v)=−hv(v+i)T− C dy1+(v−y)2,(2.5)G(v,ξ)=−1π11+a(y).(2.6)Here(αn)m n=1and(βn)m n=1are sequences of1or2.We define the number of 1in(αn)m n=1as|α+|and the position n of j-th1in(αn)m n=1asα+j:αα+j=1,1≤α+1<α+2<···<α+|α+|≤m.We also define the number of2in(βn)m n=1as|β−|and the position n of j-th2in(βn)m n=1asβ−j:ββ−j=2,31≤β−1<β−2<···<β−|β−|≤m .We shall put α+j =α+|α+|−j +1for j ∈{1,2,...,|α+|}and β−j =β−j −|α+|for j ∈{|α+|+1,|α+|+2,...,|α+|+|β−|}.The contour C surrounds the real axis anti-clockwise manner.a (v )=1/a (v ).The emptiness formation probability is a special case ofthis density matrix element:P (m )=<e j 11e j +111···e j +m−111>.In this case,the multiple integral formula (2.4)reduces to the one in [3].3High temperature expansionIn this paper,we will calculate the HTE of the following two-point correlation functions for finite magnetic field h :<σz j σz j +2>=<(e j 11−e j 22)(e j +111+e j +122)(e j +211−e j +222)>,(3.1)<σz j σz j +3>=<(e j 11−e j 22)(e j +111+e j +122)(e j +211+e j +222)(e j +311−e j +322)>,(3.2)<σ+j σ−j +2>=<e j 21(e j +111+e j +122)e j +212>.(3.3)At h =0,one can express nearest neighbor and 2nd neighbor correlationfunctions in terms of P (2),P (3):<σz j σz j +1>=4P (2)−1,<σz j σzj +2>=8(P (3)−P (2)+12<σz j σz j +2>which holds for isotropic model (XXX -model)at h =0.Moreover one can calculate the nearest neighbor correlation functions by taking the derivative of the free energy of the XXZ -chain withrespect to the anisotropy parameter.On the other hand,<σz j σzj +3>can not be expressed only in terms of P (m )even at h =0.At first,we will calculate the HTE of a (v )from the NLIE (2.5).Note that this calculation is similar to the one for the HTE for the free energy [9].We assume the following expansion for small |J/T |:a (v )=exp ∞ k =1a k (v ) J T + a 1(v )2T )2+a 1(v )3T)3(3.4)+a 1(v )42+a 2(v )2T)4+···.Substituting (3.4)into (2.5),and comparing coefficients of (J/T )m on both4sides,we obtain the following integral equation for each m (m ∈Z ≥1):a m (v )=−hv (v +i )δm,1−Cdy2+A m (y )8,A 3(y )=a 1(y )a 2(y )192,....(3.6)We can solve(3.5)recursively.The first few terms of {a m (v )}are a 1(v )=−hv (1+v 2),a 2(v )=h(1+v 2)2,a 3(v )=−h3(1+v 2)4−h (1−3v 2)2J 2(1+v 2)2−h 3Tk.(3.8)Substituting (3.8)into (2.6),we can obtain the coefficients.The first few5terms of{g k(v,ξ)}are g0(v,ξ)=−i(1+v2)(1+(v−ξ)2)(1+ξ2)+h(1+v2)(1+(v−ξ)2)(1+ξ2)2−h(2+2v2−2vξ+ξ2)2J(v2+1)2((v−ξ)2+1)(ξ2+1)2+h2(iξ−2iv)24J3((v−ξ)2+1),....(3.9)One see that only g0(v,ξ)has a pole at v=ξ.Taking note on the above results and substituting(3.4)and(3.8)into(2.4),we can calculate the coef-ficients of the HTE for the density matrix in afinite magneticfield h only by taking residues at the origin.Then we can calculate the HTE of the two point functions(3.1)-(3.3)by using the result on the HTE of matrix elements of the density matrix.For example,the HTE of a3rd neighbor correlation function at h=0up to the order of25is given as follows:<σz jσz j+3>=−t3−t4+58t545−545t7315−3227t914175+34762571t1151975−1354469786t13363825+4993399351951t15638512875−337708981437007t1732564156625+15824076710853959t19 9280784638125−1840071379448207089t21714620417135625−10941168707397851825299t23 49308808782358125+4135206247498584771500543t25h=2,4,6,8up to the order of20;<σ+jσ−j+2>for h=2,4,6,8up to the order of30.In[16,17],the HTE of correlation functions for zero magnetic field were calculated up to the order of19by other method.It is remarkable that we can also treat nonzero magneticfield case and the orders of our HTE are higher than the ones in[16,17].We have plotted the Pad´e approximations of the HTE of these correlation functions forfinite magneticfields h in Figures1-5.Once we introduce the HTE,we can also consider J<0case by analytic continuation,though original multiple integral formula(2.4)was defined for J>0case.We have also plotted quantum Monte Carlo simulation(QMC)data by Shiroishi[18] based on the open source software in the ALPS project[19,20].The system size of the simulations is L=128.Our HTE results agree well with these QMC data except in the very low temperature regions.At least in the region where the Pad´e approximation seems to converge,<σz jσz j+2>for J>0at h=0and for J<0,<σz jσz j+3>for J<0and<σ+jσ−j+2>at h=0 monotonously decrease with respect to temperature(here we omit afigure of<σz jσz j+2>for J<0);<σz jσz j+3>for J>0at h=0monotonously increases with respect to temperature.When h>0infigures1,2,5,peaks appear at non-trivial temperatures.4Concluding remarksIn this paper,we have evaluated the multiple integral formula of the density matrix by using the HTE method,and thereby obtained the HTE of several two point correlation functions.Together with our previous paper[14]on P(m),we recognized that the HTE method is efficient to evaluate the mul-tiple integral formulae of correlation functions[1]-[3].In[23],the multiple integral formula(2.4)has been reduced tofinite sums over products of single integrals for short segments of length2and3.If a similar reduction is done for length4,one will be able to calculate the HTE whose order is higher than the one in this paper.Acknowledgments We would like to thank Masahiro Shiroishi for discus-sions and providing us his unpublished QMC data[18].Mathematica Com-putation in this work was carried out at the Yukawa Institute Computer Facility.7T/J0 1 2 3 4 5 6 7 8T/JT/|J|T/J0 1 2 3 4 5 6 7T/|J|References[1]F.G¨o hmann,A.Kl¨u mper and A.Seel:J.Phys.A:Math.Gen.38(2005)1833-1841;cond-mat/0412062.[2]F.G¨o hmann,A.Kl¨u mper and A.Seel:J.Phys.A:Math.Gen.37(2004)7625–7651;hep-th/0405089.[3]F.G¨o hmann,A.Kl¨u mper and A.Seel:Physica B359-361(2005)807-809;cond-mat/0406611.[4]F.G¨o hmann, A.Seel:Theor.Math.Phys.146(2006)119-130;Teor.Mat.Fiz.146(2006)146-160;hep-th/0505091.[5]F.G¨o hmann,N.P.Hasenclever,A.Seel:J.Stat.Mech.0510(2005)P015;cond-mat/0509765.[6]M.Suzuki:Phys.Rev.B31(1985)2957–2965.[7]M.Suzuki and M.Inoue:Prog.Theor.Phys.78(1987)787–799.[8]A.Kl¨u mper:Ann.Physik1(1992)540–553;Z.Phys.B91(1993)507–519.[9]C.Destri and H.J.de Vega:Phys.Rev.Lett.69(1992)2313-2317;Nucl.Phys.B438[FS](1995)413-454;hep-th/9407117.[10]M.Suzuki:J.Stat.Phys.110(2003)945-956;Physica A321(2003)334-339.[11]M.Jimbo,K.Miki,T.Miwa and A.Nakayashiki:Phys.Lett.A168(1992)256-263.[12]M.Jimbo and T.Miwa:J.Phys.A:Math.Gen.29(1996)2923-2958.[13]N.Kitanine,J.M.Maillet,V.Terras:Nucl.Phys.B567(2000)554-582;math-ph/9907019.[14]Z.Tsuboi,M.Shiroishi:J.Phys.A:Math.Gen.38(2005)L363-L370;cond-mat/0502569.[15]M.Bortz and F.G¨o hmann:Eur.Phys.J.B46(2005)399-408;cond-mat/0504370.[16]N.Fukushima,Y.Kuramoto,J.Phys.Soc.Jpn.71(2002)1238-1241;cond-mat/0110550.13[17]N.Fukushima:J.Stat.Phys.111(2003)1049-1090;cond-mat/0212123.[18]M.Shiroishi:private communications.[19]F.Alet,P.Dayal,A.Grzesik,A.Honecker,M.Koerner,euchli,S.R.Manmana,I.P.McCulloch,F.Michel,R.M.Noack,G.Schmid,U.Schollwoeck,F.Stoeckli,S.Todo,S.Trebst,M.Troyer,P.Werner,S.Wessel:J.Phys.Soc.Jpn.Suppl.74(2005)30-35;cond-mat/0410407.(see also )[20]F.Alet,S.Wessel and M.Troyer:Phys.Rev.E71(2005)036706;cond-mat/0308495.[21]M.Takahashi:J.Phys.C10(1977)1289-1301.[22]K.Sakai,M.Shiroishi,Y.Nishiyama and M.Takahashi:Phys.Rev.E67(2003)065101(R);cond-mat/0302564.[23]H.E.Boos,F.G¨o hmann,A.Kl¨u mper,J.Suzuki:J.Stat.Mech.0604(2006)P001;hep-th/0603064.14。

高二英语科学概念高级应用单选题45题

高二英语科学概念高级应用单选题45题

高二英语科学概念高级应用单选题45题1.The force acting on an object is directly proportional to its acceleration. If the force on an object is doubled, its acceleration will _____.A.be halvedB.remain the sameC.be doubledD.be quadrupled答案:C。

解析:根据牛顿第二定律F=ma,力与加速度成正比。

当力加倍时,加速度也会加倍。

A 选项加速度减半错误;B 选项加速度不变错误;D 选项加速度变为四倍错误。

2.In an electromagnetic field, the direction of the magnetic field is perpendicular to the direction of the electric field. If the electric field points north, the magnetic field cannot point _____.A.eastB.southC.westD.north答案:D。

解析:因为磁场方向与电场方向垂直,所以当电场指向北时,磁场不能指向北。

A 选项东与北垂直,有可能;B 选项南与北垂直,有可能;C 选项西与北垂直,有可能。

3.When an object is in equilibrium, the sum of all forces acting on it is _____.A.zeroB.greater than zeroC.less than zeroD.indeterminate答案:A。

解析:物体处于平衡状态时,所受合力为零。

B 选项大于零错误,物体将有加速度;C 选项小于零错误,同理;D 选项不确定错误。

4.The work done on an object is equal to the force applied multiplied by the distance moved in the direction of the force. If a force of 10 N moves an object 5 meters in its direction, the work done is _____.A.2 JB.50 JC.15 JD.25 J答案:B。

2024年高一英语气候科学研究进展单选题40题

2024年高一英语气候科学研究进展单选题40题

2024年高一英语气候科学研究进展单选题40题1.Climate change is mainly caused by the increase in _____.A.greenhouse gasesB.ozone layerC.pollutantsD.water vapor答案:A。

温室气体的增加是气候变化的主要原因。

选项B 臭氧层主要起到阻挡紫外线的作用,与气候变化的主要原因关系不大。

选项 C 污染物的范围比较广,不是气候变化的主要原因。

选项 D 水汽也不是气候变化的主要原因。

2.The phenomenon of global warming is closely related to _____.A.carbon dioxide emissionsB.air pollutionC.water pollutionD.soil pollution答案:A。

全球变暖现象与二氧化碳排放密切相关。

选项B 空气污染不是全球变暖的直接主要原因。

选项C 水污染与全球变暖关系不大。

选项D 土壤污染也与全球变暖没有直接关系。

3.The term “El Niño” refers to _____.A.a weather patternB.a climate change phenomenonC.an ocean currentD.a type of storm答案:A。

“厄尔尼诺”是一种天气模式。

选项B 它不是气候变化现象本身。

选项C 它不是洋流。

选项D 它不是一种风暴。

4.The “greenhouse effect” is caused by _____.A.the absorption of heat by the atmosphereB.the reflection of sunlight by the EarthC.the emission of heat by the SunD.the cooling of the Earth答案:A。

温度升高万物生长英语作文

温度升高万物生长英语作文

温度升高万物生长英语作文As the global temperatures continue to rise, the effects onthe natural world are becoming increasingly apparent. The phenomenon of global warming has far-reaching consequences, affecting everything from the behavior of animal species tothe growth patterns of plant life. This essay will explorethe various ways in which rising temperatures are influencing the growth and development of living organisms.Firstly, the increase in temperature can lead to longer growing seasons for many plants. This extended period of warmth allows for a surge in growth, as plants have more time to photosynthesize and produce food. However, this can also mean that certain species may outcompete others for resources, leading to shifts in the composition of ecosystems.Secondly, warmer temperatures can affect the timing of biological events, such as flowering in plants and migrationin animals. For instance, some plants may flower earlier inthe year, which can disrupt the life cycles of pollinatorsthat rely on these plants for food. Similarly, changes in the timing of animal migrations can have cascading effects on predator-prey relationships and the overall balance of food webs.Thirdly, rising temperatures can also influence thedistribution of species. Some species may move to higher altitudes or latitudes in search of cooler temperatures,which can lead to the colonization of new habitats and potentially the displacement of native species.Moreover, the increased temperature can lead to more frequent and severe heatwaves, which can be detrimental to many forms of life. Heat stress can cause physiological damage to plants and animals, reducing their ability to grow, reproduce, and survive.Lastly, the impact of higher temperatures on the growth of organisms is not solely direct. Indirect effects include changes in precipitation patterns, which can lead to droughts or floods, both of which can significantly affect the growth and survival of various species.In conclusion, the rise in global temperatures is a complex issue with profound implications for the growth and survival of all living organisms. It is crucial for scientists, conservationists, and policymakers to continue studying these effects and to develop strategies to mitigate the impacts of climate change on biodiversity.。

中国石油大学高级英语译文及答案

中国石油大学高级英语译文及答案

Unit 1 Sources of EnergyText APetroleumSentence structure analysis1. Instead of originating in accumulating woody matter, petroleum may be the product of the accumulating fattymatter of ocean organisms such as plankton, the myriads of single-celled creatures that float in the surface layer of the ocean. (Para.2) 石油,并不是来自于逐渐积聚的木质物质,而可能是来自于逐渐积聚的海洋生物的脂肪物质。

比如浮游生物:大量浮游在海水表层的单细胞生物。

这是一个简单句,主语petroleum,谓语动词may be,表语product,构成句子主干。

instead of 介词短语作状语,such as plankton是product一词的同位语,the myriads of single-celled creatures that float in the surface layer of the ocean是名词性短语,做plankton的同位语。

2. It is only necessary that the organisms settle down into the ooze underlying shallow arms of the ocean underconditions of oxygen shortage. (Para. 3) 生物有机体只需在缺氧的条件下沉积到海湾浅水处的淤泥里。

该句的框架为:it is +adj.+that从句,it做形式主语,真正的主语是that从句的内容。

现在分词短语underlying…做后置定语修饰ooze。

分子筛特殊再生方案

分子筛特殊再生方案

Yulin TSA INITIAL CONDITIONING PROCEDUREPurposeThe TSA’s contain a layer of CaX material to remove CO2and N2O.Water typically does not contact this layer.But under some plant upsets maintenance,or during loading of sieve;water may reach this material.As the residual water content on the CaX increases,its capacity for CO2and N2O decreases,which can lead to premature break through(i.e.shorter on-stream times).Normal regeneration temperatures are not high enough to completely remove water from the CaX material,so high temperature regeneration is required.This procedure describes the steps for the initial regeneration of the TSA.ScopeThis procedure assumes the ASU has been isolated and secured,such that it is safe to operate the main air compressor,DCAC,and the TSA.Warnings/NotesThe high temperature regeneration causes a few situations that must be monitored closely.∙The TSA regeneration circuit isn’t designed for high temperature and pressure.The regeneration circuit pressure must operate<0.5bar g∙The temperature to the main exchanger<65C.∙Ensure the area around the TSA and Regeneration Heaters is clear.∙The minimum regeneration flow rate is13,700Nm3/hr.If the regeneration flow is too low it won’t be effective in removing the water or steaming of the sieve could occur.∙Breakthrough of CO2(>50ppm CO2)onto a hot bed could cause some damage to the sieve.∙In order to achieve the desired effect,the total heat time for each adsorber vessel must be>12hours with regeneration flow conditions of14500Nm3/hr at300Cregen inlet temp.Assume heater outlet temp is330C to account for piping heat leak.∙The on-line time for the adsorber is about30hours at33C air inlet temperature and 15000Nm3/hr of air flow.∙TSA on line time for adsorber can be increased if air temperature is lower.At15000 nm3/h bootstrap flow,28C and5barg inlet conditions,the on stream time is approx 38hours.∙The steam and electric heaters must be run to achieve the330C regeneration temperature.∙During regen,air flow to the on stream adsorber should be limited to the adsorber regeneration flow of14500Nm3/hr to minimize on stream adsorber water load and maximize on stream time.Procedure1.Start the MAC,Front end system.主压缩机,空冷塔和TSA正常运转。

以全球气候变暖导致水平面上升的英语作文

以全球气候变暖导致水平面上升的英语作文

以全球气候变暖导致水平面上升的英语作文全文共3篇示例,供读者参考篇1The Big Wet ProblemDid you know the oceans are getting bigger and bigger? I didn't realize it at first, but my teacher Mrs. Green taught us all about it in science class. She said it's a huge problem caused by global warming that could flood lots of cities and islands if we don't do something about it soon.So what's going on exactly? Well, the earth is getting hotter overall because of things like burning too much coal, oil and gas for energy, cutting down forests, and polluting the air with gases from cars, factories and farms. All that extra heat is melting the big ice sheets in Greenland and Antarctica.When that ice melts, the water runs into the oceans and seas, making the level go up higher and higher. It's kind of like if you have a glass of water with some ice cubes, and the ice cubes start to melt - the water level in the glass rises. Except in this case, the glass is our whole planet!Mrs. Green showed us some pictures of islands in the Pacific Ocean that are already being flooded because of rising seas. Some of the houses were surrounded by water up to the windows! In other places, the ocean was creeping over coastal roads and parks. She said at the current rate, sea levels could rise over 2 feet by the year 2100. That may not sound like much, but it's enough to cause big problems.Big cities like New York, Miami, Los Angeles, Shanghai, Mumbai and many others are right along the coast. Even a small sea level rise of a few inches could lead to more flooding from storm surges when hurricanes hit. And a rise of several feet means parts of those cities could wind up underwater! Millions of people might have to move inland to stay dry.Islands countries in the Pacific and Caribbean could be in even bigger trouble since they are so tiny and flat, with shores very close to sea level already. Some whole islands may disappear completely one day if we don't stop the oceans from rising.It's a scary thought to imagine your house, school, or whole town being swallowed up by the sea. I really don't want that to happen here or anywhere else. So what can we do about it?The main cause of all this, like I said, is global warming from human activities pumping too many greenhouse gases into the air. So we need to find ways to cut down on those gases. We can use more renewable energy like solar and wind instead of burning coal and oil. We can drive less and walk, bike, or take the bus more. We can plant more trees to absorb carbon dioxide. And we can reduce, reuse, and recycle more to cut down on waste.It will take cooperation from everyone - kids, parents, teachers, world leaders, scientists and more - to make big changes. But we have to do it, because the alternative of rising seas is too sad and scary. Just imagine your favorite beach getting smaller and smaller until it disappears under the waves. Or imagine having to move away from your home because it's flooded. Those things could really happen if we don't take action now.I'm going to do my part by recycling more, walking to school instead of getting rides, and reminding my family to turn off lights and appliances when not using them. Mrs. Green said even small actions can help a lot when millions of people do them. I'll also tell my friends and neighbors about this big wet problem so they can help too.It might seem weird to think about the whole world's oceans rising up. But the science is clear - it's happening because of global warming, and it will keep happening faster unless we change our habits. I don't want my future kids or grandkids to have an even bigger mess on their hands. We need to take better care of our planet, starting right now, before it's too late.篇2Sea Level Rise: The Threat of Rising WatersHi everyone! My name is Jamie, and I'm here to talk to you about something that's really important and could affect all of us – sea level rise.You might be wondering, "What is sea level rise?" Well, it's when the level of the oceans around the world starts to get higher and higher. And you know what's causing it? Global warming!Global warming is making the Earth's temperature go up little by little. This warming is happening because of things like pollution from factories, cars, and other human activities that release something called greenhouse gases into the air. These gases trap heat from the sun and make the Earth warmer than it should be.So, how does global warming cause sea levels to rise? There are a few reasons:Melting glaciers and ice sheets: You know those huge masses of ice that cover places like Greenland and Antarctica? They're called glaciers and ice sheets. Well, as the Earth gets warmer, that ice starts to melt. And when all that ice melts, it turns into water that flows into the oceans, making them rise higher and higher.Thermal expansion: This might sound like a complicated term, but it's actually pretty simple. Basically, when water gets warmer, it expands and takes up more space. So, as the oceans get warmer because of global warming, the water in them expands, causing the sea level to rise.Now, you might be thinking, "But the oceans are so big! How much can the sea level really rise?" Well, let me tell you, even a small rise in sea level can be really dangerous.For people who live in coastal areas or on islands, a rising sea level can cause flooding, which can damage homes, businesses, and roads. It can also make it harder for people to get clean drinking water, since seawater can contaminate freshwater sources.And it's not just people who are affected. Rising sea levels can also harm animals and plants that live near the coast. Their homes and habitats can be flooded or washed away, making it hard for them to survive.But that's not all! Even if you don't live near the coast, sea level rise can still affect you. It can cause more severe storms and hurricanes, which can bring flooding and destruction to inland areas too.So, what can we do about this? Well, the most important thing is to try to stop global warming from getting worse. We need to find ways to reduce our greenhouse gas emissions, like using renewable energy sources like solar and wind power instead of burning fossil fuels like coal and oil.We also need to protect coastal areas and wetlands, which can help absorb some of the water from rising seas. And we need to be prepared for the changes that are already happening by building better flood defenses and planning for how to deal with sea level rise.But you know what? Even though this might sound scary, I believe that if we all work together, we can find ways to solve this problem. Scientists and engineers are working on newtechnologies to help us, and lots of people are trying to live in more environmentally friendly ways.And you know what else? Kids like us can help too! We can learn about this issue and share what we know with our friends and families. We can also do little things like turning off lights when we're not using them, recycling, and walking or riding our bikes instead of taking a car.Every little bit helps, and if we all work together, we can make a difference. So let's get started and do our part to protect our planet from sea level rise!篇3The Watery WorldThe Earth is a wonderful planet that we all call home. It has majestic mountains, lush green forests, and vast blue oceans. But something is happening to our planet that is causing big problems, especially for the oceans. It's called global warming, and it's making the oceans rise higher and higher. Let me tell you all about it.Global warming happens when there is too muchheat-trapping gas in the air. This gas is called carbon dioxide, and it comes from things like factories, power plants, and cars.When there's a lot of carbon dioxide in the air, it acts like a thick blanket that traps the heat from the sun close to the Earth's surface. This trapped heat makes the Earth warmer than it should be, causing what we call the "greenhouse effect."As the Earth gets warmer, some very strange things start to happen. One of the biggest problems is that the ice at the North and South Poles starts to melt. You see, these polar ice caps are made of frozen water that has been around for thousands of years. But when the Earth's temperature rises, even a little bit, this ancient ice begins to turn into liquid water.Now, you might be thinking, "So what? Let the ice melt –we'll just have more water to drink!" But the problem is, this melted ice water doesn't stay in the polar regions. Instead, it flows into the oceans, adding more and more water to the seas. And when you add more water to something that's already full, like the oceans, it has to go somewhere. That's why the sea levels are rising!But that's not the only reason the oceans are getting higher. You see, water expands when it gets warmer, just like how a balloon gets bigger when you blow air into it. As the Earth's temperature rises, the water in the oceans is also getting warmer, causing it to take up more space and rise higher.So, with melting ice from the poles and the expansion of warmer ocean water, the sea levels are rising at an alarming rate. Scientists predict that by the end of this century, the oceans could be up to three feet higher than they are now! That might not sound like much, but it's enough to cause big problems for many coastal cities and islands around the world.Imagine if you lived in a place like Miami, Florida, or the Island of Tuvalu in the Pacific Ocean. These low-lying areas could be completely flooded by the rising seas, forcing people to leave their homes and find new places to live. Even cities that aren't right on the coast, like New York or London, could experience more flooding and storm surges because of the higher sea levels.But it's not just humans who will be affected by rising seas. Many animals and plants that live in coastal areas could lose their habitats as the water levels rise. Beaches could disappear, and wetlands could be submerged, destroying the homes of countless species.It's a scary thought, isn't it? A world where the oceans are constantly creeping higher and higher, swallowing up land and forcing people and animals to flee. But there is hope! We can all do our part to slow down global warming and sea level rise.One of the most important things we can do is to reduce our carbon footprint, which means cutting down on the amount of carbon dioxide we release into the air. We can do this by using less electricity, driving less, and recycling more. We can also plant more trees, which absorb carbon dioxide and release oxygen back into the air.Governments and businesses also need to take action by switching to cleaner energy sources, like solar and wind power, and by making their factories and vehicles more energy-efficient.It might seem like a big challenge, but if we all work together, we can make a difference. Every little bit helps, whether it's turning off the lights when you leave a room or walking to school instead of taking the bus. Because the truth is, we only have one planet, and it's our job to take care of it.So let's do our part to keep the Earth healthy and the oceans at a safe level. Let's work together to create a future where our children and grandchildren can enjoy the beauty of our planet, just like we do now. A future where the oceans are still vast and blue, and the land is safe and dry. It's up to us to make it happen!。

高温天气英语作文1

高温天气英语作文1

Title: Coping with the Intense Heatwave: Strategies and ReflectionsAs the global climate continues to undergo significant changes, intense heatwaves have become an increasingly common occurrence, posing challenges to our daily lives, health, and even the environment. In this essay, we will delve into the impact of high-temperature weather, explore effective strategies for coping with it, and reflect on the longer-term implications for society.The Impact of High-Temperature WeatherFirstly, let's acknowledge the immediate impact of heatwaves. For humans, prolonged exposure to extreme heat can lead to heat exhaustion, heat stroke, and even death, especially among the elderly, young children, and those with pre-existing health conditions. Additionally, the high temperatures strain power grids, causing blackouts and disruptions to essential services. Crops suffer, waterways dry up, and wildlife faces significant challenges in finding food and shelter. Furthermore, air quality deteriorates due to increased ground-level ozone, exacerbating respiratory issues. Strategies for CopingStay Hydrated: Drink plenty of water throughout the day, even if you don't feel thirsty. Avoid sugary drinks and caffeinated beverages, which can actually dehydrate you further.Limit Outdoor Exposure: When possible, avoid direct sunlight during the hottest hours of the day (typically between 10 am and 4 pm). If you must go outside, wear light-colored, loose-fitting clothing and a wide-brimmed hat to protect yourself from the sun.Use Air Conditioning Wisely: Air conditioning can provide relief from the heat, but it's important to use it efficiently to conserve energy. Set the thermostat to a comfortable temperature (around 24-26°C) and use fans to circulate the air.Check on Vulnerable Individuals: Make sure to regularly check on elderly neighbors, friends, or relatives who may be at risk of heat-related illnesses.Plan Ahead: If you're traveling, research the weather conditions in advance and plan your itinerary accordingly. Bring extra water and sunscreen, and consider postponing outdoor activities during peak heat hours.Promote Green Spaces: Urban green spaces like parks and gardens can help cool down cities by providing shade and evaporative cooling. Encourage the development and preservation of these areas in your community.Longer-Term Implications and SolutionsBeyond individual coping strategies, we must also address the root causes of climate change, which is largely responsible for the frequency and intensity of heatwaves. This includes reducing greenhouse gas emissions through sustainable practices such as energy efficiency, renewable energy adoption, and reduced consumption. Governments and businesses have a crucial role to play in setting ambitious climate targets and implementing policies that incentivize these changes.Additionally, investing in heatwave preparedness and response systems is vital. This includes early warning systems, public education campaigns, and emergency response plans to ensure that communities are equipped to handle the health and infrastructure impacts of extreme heat.In conclusion, coping with intense heatwaves requires a multi-faceted approach that combines individual actions, community support, and policy interventions. By adopting these strategies and addressing the underlying causes of climate change, we can mitigate the impacts of high-temperature weather and build a more resilient future for all.。

关于极端高温的英语作文

关于极端高温的英语作文

Extreme High Temperatures: Impacts, Challenges, and SolutionsExtreme high temperatures have become a global phenomenon, posing significant challenges to our planet and its inhabitants. These record-breaking heat waves are not just uncomfortable, but they also have profound impacts on our environment, health, economy, and society.Firstly, the environmental impact of extreme high temperatures is alarming. Prolonged heatwaves lead to accelerated melting of ice caps and glaciers, contributing to sea level rise and the disruption of ecosystems. Additionally, hotter temperatures can lead to increased evaporation, altering rainfall patterns and affecting water availability. This, in turn, has a direct impact on agriculture and food security, as crops suffer from drought and heat stress.Moreover, the health consequences of extreme heat are numerous and severe. Heatwaves can lead to heat exhaustion and heatstroke, especially among the elderly, children, and those with pre-existing health conditions. The rise in temperature also increases the risk of vector-bornediseases like dengue and malaria, as mosquitoes and other insects thrive in warmer climates.Furthermore, the economy also bears the brunt ofextreme high temperatures. Heatwaves disrupt supply chains, affecting production and distribution of goods and services. The tourism industry, particularly in coastal areas, isalso affected as the sweltering heat drives away tourists. Additionally, the demand for cooling systems and air conditioning skyrockets, leading to increased energy consumption and greenhouse gas emissions.Finally, the social impact of extreme heat is also significant. Heatwaves disrupt daily life, forcing peopleto stay indoors and avoid outdoor activities. This can lead to isolation and mental health issues, especially during prolonged heatwaves. Moreover, the unequal distribution of heat exposure often results in social disparities, with certain communities, such as those living in urban heat islands or low-income areas, disproportionately affected.In light of these challenges, it is imperative that we take action to address extreme high temperatures. Onecrucial step is to reduce greenhouse gas emissions andmitigate climate change. This involves promoting renewable energy sources, improving energy efficiency, and adopting sustainable practices in all sectors. Additionally, we need to enhance our resilience to heatwaves by improving infrastructure and urban design to reduce the urban heat island effect.Moreover, it is essential to strengthen public health systems and provide heatwave warnings and advice to vulnerable populations. This includes educating the public on heat-related illnesses and providing access to cooling centers during extreme heat events.Furthermore, policies and regulations need to be formulated to address the social disparities caused by heatwaves. This includes ensuring that all communities have access to cooling facilities and resources, and that vulnerable populations are prioritized in heatwave response plans.In conclusion, extreme high temperatures pose significant threats to our planet and society. By taking action to mitigate climate change, enhance resilience, and address social disparities, we can reduce the impacts ofheatwaves and create a more sustainable and resilientfuture for all.**极端高温:影响、挑战与解决方案**极端高温已经成为全球性的现象,给我们的星球和居民带来了巨大挑战。

高中英语语新闻练习题 72

高中英语语新闻练习题 72

英语新闻-填词Chinese scientists develop ultrastrong, high thermal insulating ceramicsChinese scientists have created a new porous ceramic that is ultrastrong at elevated temperatures and simultaneously high thermal insulating, two properties needed for making the shell of hypersonic aircraft.The team, 1 Chu Yanhui from the South China University of Technology, developed porous high-entropy diboride ceramics exhibiting remarkable load-carrying capability, high thermal insulating performance, and superior thermal stability of up to 2,000 degrees Celsius. Such features have made it an attractive option for reliable thermal insulation under extreme conditions, according to the university.Searching for a porous ceramic that is both strong and resistant to extreme heat has been a holy grail for material scientists with the advent of hypersonic flight technologies. The two features, however, are difficult to achieve simultaneously in 2 porous ceramics, whose previous record of maximum temperature stood at 1,500 degrees Celsius.Researchers said the new material has broad 3 prospects in the aerospace, energy, and chemical industries.英语新闻-语法填空Chinese scientists develop ultrastrong, high thermal insulating ceramicsChinese scientists have created a new porous ceramic that is ultrastrong at elevated temperatures and simultaneously high thermal insulating, two 1 (property) needed for making the shell of hypersonic aircraft.The team, led by Chu Yanhui from the South China University of Technology, developed porous high-entropy diboride ceramics exhibiting 2 (remark) load-carrying capability, high thermal insulating performance, and superior thermal stability of up to 2,000 degrees Celsius. Such features have made it an attractive option for reliable thermal insulation under extreme conditions, according to the university.Searching for a porous ceramic that is both strong and resistant to extreme heat has been a holy grail for material scientists with the advent of hypersonic flight technologies. The two features, however, are difficult to achieve simultaneously in conventional porous ceramics, whose previous record of maximum temperature stood 3 1,500 degrees Celsius.Researchers said the new material has broad application prospects in the aerospace, energy, and chemical industries.中文新闻:中国科学家开发出超强、高绝热陶瓷中国科学家发明了一种新型多孔陶瓷,它在高温下超强,同时具有高绝热性,这是制造高超音速飞机外壳所需的两种特性。

(整理)科普知识学英语 海水表面温度达近150年来最高

(整理)科普知识学英语 海水表面温度达近150年来最高

Sea surface temperatures in the Northeast Shelf Large Marine Ecosystem during 2012 were the highest recorded in 150 years, according to the latest Ecosystem Advisory issued by NOAA's Northeast Fisheries Science Center (NEFSC). These high sea surface temperatures (SSTs) are the latest in a trend of above average temperature seen during the spring and summer seasons, and part of a pattern of elevated temperatures occurring in the Northwest Atlantic, but not seen elsewhere in the ocean basin over the past century. The advisory reports on conditions in the second half of 2012.Sea surface temperature for the Northeast Shelf Ecosystem reached a record high of 14 degrees Celsius (57.2°F) in 2012, exceeding the previous record high in 1951. Average SST has typically been lower than 12.4 C (54.3 F) over the past three decades.Sea surface temperature in the region is based on both contemporary satelliteremote-sensing data and long-term ship-board measurements, with historical SST conditions based on ship-board measurements dating back to 1854. The temperature increase in 2012 was the highest jump in temperature seen in the time series and one of only five times temperature has changed by more than 1 C (1.8 F).The Northeast Shelf's warm water thermal habitat was also at a record high level during 2012, while cold water habitat was at a record low level. Early winter mixing of the water column went to extreme depths, which will impact the spring 2013 plankton(浮游生物) bloom. Mixing redistributes nutrients and affects stratification of the water column as the bloom develops.Temperature is also affecting distributions of fish and shellfish on the Northeast Shelf. The advisory provides data on changes in distribution, or shifts in the center of the population, of seven key fishery species over time. The four southern species -- black sea bass, summer flounder, longfin squid and butterfish -- all showed a northeastward or upshelf shift. American lobster has shifted upshelf over time but at a slower rate than the southern species. Atlantic cod and haddock(黑线鳕)have shifted downshelf.""Many factors are involved in these shifts, including temperature, population size, and the distributions of both prey and predators," said Jon Hare, a scientist in the NEFSC's Oceanography Branch. A number of recent studies have documented changing distributions of fish and shellfish, further supporting NEFSC work reported in 2009 that found about half of the 36 fish stocks studied in the Northwest Atlantic Ocean, many of them commercially valuable species, have been shifting northward over the past four decades.在东北保质大型海洋生态系统在2012年的海表面温度最高记录150年来,根据最新的生态系统咨询由NOAA的东北渔业科学中心(NEFSC)发行。

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DFT-IF-UERJ-99/10
High Temperature Resummation in the Linear δ -Expansion
Marcus B. Pinto1
1 ∗
and Rudnei O. Ramos2

2
arXiv:hep-ph/9903353v2 3 Aug 1999
Departamento de F´ ısica, Universidade Federal de Santa Catarina, 88.040-900 Florian´ opolis, SC, Brazil Departamento de F´ ısica Te´ orica - Inst. de F´ ısica, Universidade do Estado do Rio de Janeiro, 20.550-013 Rio de Janeiro, RJ, Brazil
II. THE LINEAR δ-EXPANSION APPLIED TO THE EVALUATION OF THE THERMAL MASS IN THE λφ4 THEORY
1
A. The Linear δ-Expansion
The optimized linear δ -expansion is an alternative nonperturbative approximation which has been successfully used in a plethora of different problems in particle theory [15,17–19], quantum mechanics [20,21] statistical physics [22], nuclear matter [23] and lattice field theory [24]. One advantage of this method is that the selection and evaluation (including renormalization) of Feynman diagrams are done exactly as in ordinary perturbation theory using a very simple modified propagator which depends on an arbitrary mass parameter. Nonperturbative results are then obtained by fixing this parameter. An interesting result obtained with this method in the finite temperature domain is given in Ref. [18] where the critical temperature value for the Gross-Neveu model in 1+1 dimensions nicely converges, order by order, towards the exact result set by Landau’s theorem (Tc = 0) 1 . The sinear δ -expansion to a theory described by a Lagrangian density L starts with an interpolation defined by Lδ = (1 − δ )L0 (η ) + δ L = L0 (η ) + δ [L − L0 (η )], (2.1) where L0 (η ) is the Lagrangian density of a solvable theory which can contain an arbitrary mass parameter (η ). The Lagrangian density Lδ interpolates between the solvable L0 (η ) (when δ = 0) and the original L (when δ = 1). In this work we consider the λφ4 model described by 1 1 λ L = (∂µ φ)2 − m2 φ2 − φ4 + Lct , 2 2 4! where 1 1 λ Lct = A (∂µ φ)2 − B m2 φ2 − Cφ4 2 2 4! (2.3) (2.2)
Abstract
The optimized linear δ-expansion is applied to the λφ4 theory at high temperature. Using the imaginary time formalism the thermal mass is evaluated perturbatively up to order δ2 . A variational procedure associated with the method generates nonperturbative results which are used to obtain the critical temperature for the phase transition. Our results are compared with the ones given by propagator dressing methods. PACS number(s): , 12.38.Lg
∗ E-mail: † E-mail:
fsc1mep@fsc.ufsc.br rudnei@dft.if.uerj.br
I. INTRODUCTION
The breakdown of perturbation expansion in high temperature quantum field theory is a well known problem [1,2] whose solution is still a matter of study and discussion today, with different authors using different methods [3–11]. High temperature perturbation expansion breaks down due to the appearance of infrared divergences close to critical temperatures (in field theories displaying a second order phase transition or a weakly first order transition [12,13]), or for massless field theories, like QCD. In particular, there are parameter regimes where conventional perturbation schemes become unreliable at high temperature when powers of the coupling constants become surmounted by powers of the temperature. In general, these problems are treated with resummation techniques which try to account, in a self-consistent way, for the leading contributions in the infrared region. Among these schemes are the popular daisy and super-daisy schemes [3,4], composite operator method [6] and field propagator dressing methods [7,8]. Some of these resummation methods have been compared in Ref. [9], where their difficulties and possible caveats have also been discussed. The majority of approaches used within this subject have a potential drawback concerning the achievement of self-consistency as higher order diagrams are resummed. This happens because the dressed propagator changes order by order. Therefore, special care must be taken when selecting the correct order in the coupling constants. Another problem associated with some of these methods is related to the implementation of renormalization, as discussed in Ref. [11]. In this paper, we apply the optimized linear δ -expansion [14,15] (for earlier references see, e.g., [16]) to the λφ4 theory obtaining the thermal mass to second order in the perturbative parameter δ . Our results show that the use of a proper optimization scheme is equivalent to solve the gap equation for the thermal mass, where leading and higher order infrared regularizing contributions are nonperturbatively taken into account. An advantage of the linear δ -expansion is that the same simple propagator is used in the evaluation of any diagram, avoiding the potential bookkeeping problems mentioned above. This makes the method particularly useful and simple to use in different applications, including the study of nonperturbative high temperature effects. This work is organized as follows. In Sec. II we briefly describe the linear δ -expansion technique and then use it to evaluate the thermal mass up to order δ 2 in the 3+1d λφ4 theory. Details of the renormalization up to this order are given in Sec. III where we also discuss renormalization at higher orders in δ . We show that it does not present any additional difficulty when compared to renormalization in the usual perturbative or loop expansions. In Sec. IV we present our results for the thermal mass, including the critical temperature for the phase transition, and compare them with other results found in the literature. In Sec. V concluding remarks are given.
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