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Modulating the Electrolyte Inner Solvation Structure via Low Polarity Co-solvent for Low-Temperature Aqueous Zinc-Ion Batteries 被引量:1
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作者 Yongchao Kang Feng Zhang +6 位作者 Houzhen Li Wangran Wei Huitong Dong Hao Chen Yuanhua Sang Hong Liu Shuhua Wang 《Energy & Environmental Materials》 SCIE EI CAS CSCD 2024年第5期104-113,共10页
Aqueous zinc-ion batteries are regarded as the promising candidates for large-scale energy storage systems owing to low cost and high safety;however,their applications are restricted by their poor low-temperature perf... Aqueous zinc-ion batteries are regarded as the promising candidates for large-scale energy storage systems owing to low cost and high safety;however,their applications are restricted by their poor low-temperature performance.Herein,a low-temperature electrolyte for low-temperature aqueous zinc-ion batteries is designed by introducing low-polarity diglyme into an aqueous solution of Zn(ClO_(4))_(2).The diglyme disrupts the hydrogenbonding network of water and lowers the freezing point of the electrolyte to-105℃.The designed electrolyte achieves ionic conductivity up to16.18 mS cm^(-1)at-45℃.The diglyme and ClO_(4)^(-)reconfigure the solvated structure of Zn^(2+),which is more favorable for the desolvation of Zn^(2+)at low temperatures.In addition,the diglyme effectively suppresses the dendrites,hydrogen evolution reaction,and by-products of the zinc anode,improving the cycle stability of the battery.At-20℃,a Zn‖Zn symmetrical cell is cycled for 5200 h at 1 mA cm^(-2)and 1 mA h cm^(-2),and a Zn‖polyaniline battery achieves an ultra-long cycle life of 10000 times.This study sheds light on the future design of electrolytes with high ionic conductivity and easy desolvation at low temperatures for rechargeable batteries. 展开更多
关键词 aqueous zinc-ion batteries high performance inner solvation structure low polarity co-solvent low-temperature electrolyte
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Effect of Co-solvent and Pressure on the Thermal Decomposition of 2,2′Azobis-(isobutyronitrile) in Supercritical CO_2 被引量:1
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作者 Hong Ping LI Jun LIU +1 位作者 Hai Fei ZHANG Bu Xing HAN 《Chinese Chemical Letters》 SCIE CAS CSCD 2001年第8期713-714,共2页
The thermal decomposition of 2, 2'-azobis (isobutyronitrile) (AIBN) in supercritical CO2 with cosolvent methanol or cyclohexane has been studied by using UV/Vis spectroscopic method at 335.15 K and at 12.0 MPa and... The thermal decomposition of 2, 2'-azobis (isobutyronitrile) (AIBN) in supercritical CO2 with cosolvent methanol or cyclohexane has been studied by using UV/Vis spectroscopic method at 335.15 K and at 12.0 MPa and 14.0 MPa. Both of the cosolvents can accelerate the decomposition rate, and the effect of methanol is more significant than that of the cyclohexane. 展开更多
关键词 Supercritical CO2 co-solvent 2 2′-Azobis(isobutyronitrile) thermal decomposition pressure effect.
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Dispersion of ZnO Nanocrytals in Co-solvent and Its Application in Photovoltaic Material 被引量:1
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作者 CHEN Shao-jie ZHANG Qiu-yu ZHANG Jun-ping GU Jun-wei ZHOU Jian SHI You-qiang 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2011年第6期906-909,共4页
To overcome the aggregation of nanocrystals in a blend of inorganic material with conjugated polymers to prepare photovoltaic material, we used a co-solvent blend of CHCl3 with MeOH at a certain volume fraction to dis... To overcome the aggregation of nanocrystals in a blend of inorganic material with conjugated polymers to prepare photovoltaic material, we used a co-solvent blend of CHCl3 with MeOH at a certain volume fraction to disperse inorganic nanocrystals. The results show that when the volume fraction of MeOH is 50%, ZnO nanocrystals with an average diameter of 30 nm disperse well in the co-solvent solution. Its application in photovoltaic material was investigated in this work, and the photoluminescence(PL) spectra show that when ZnO was 50%(volume fraction) in solution and 25%(volume fraction) in film, the fluorescence quenching reached the maximum values 83.34% and 64.4%, respectively, indicating that electron could transfer from conjugated polymer to electron-acceptor ZnO effectively. 展开更多
关键词 ZnO nanocrystal DISPERSION co-solvent Photovoltaic material
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Influence of Co-Solvent on the Extraction Behaviour of Uranium and Thorium Nitrates with Organophosphorous Compounds 被引量:1
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作者 K. C. Pitchaiah K. Sujatha +4 位作者 C. V. S. Brahmmananda Rao N. Sivaraman T. G. Srinivasan K. Nagarajan P. R. Vasudeva Rao 《International Journal of Analytical Mass Spectrometry and Chromatography》 2014年第2期33-42,共10页
Supercritical Fluid Extraction (SFE) is emerging as a powerful technique in the extraction of metal ions. In the present study, the extraction of nitrates of uranium and thorium was carried out using supercritical car... Supercritical Fluid Extraction (SFE) is emerging as a powerful technique in the extraction of metal ions. In the present study, the extraction of nitrates of uranium and thorium was carried out using supercritical carbon dioxide (Sc-CO2) modified with various organophosphorous compounds such as dialkylalkyl phosphonates, trialkyl phosphates and trialkyl phosphine oxides in the presence of co-solvents such as methanol, dichlormethane and n-hexane. The influence of ligand and co-solvent on the extraction of the metal nitrates was studied in detail. These studies have established that co-solvent plays an important role in the extraction as well as fractionation of uranium and thorium nitrates. Polar co-solvent, methanol provided faster extraction without fractionation whereas the non-polar solvent, e.g. n-hexane provided some fractionation of metal nitrates though the extraction kinetics was slower. 展开更多
关键词 co-solvent URANIUM and THORIUM ORGANOPHOSPHOROUS COMPOUNDS
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Supercritical Synthesis of Ethyl Esters via Transesterification from Waste Cooking Oil Using a Co-Solvent 被引量:1
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作者 Tapaswy Muppaneni Harvind K. Reddy Shuguang Deng 《Journal of Environmental Protection》 2015年第9期986-994,共9页
Biofuels became more promising alternative to the fossil fuels because of the depletion of fossil resources, renewability, environmental benefits, and energy security. Ethanolysis of waste cooking oil with hexane as c... Biofuels became more promising alternative to the fossil fuels because of the depletion of fossil resources, renewability, environmental benefits, and energy security. Ethanolysis of waste cooking oil with hexane as co-solvent was carried out for the production of fatty acid ethyl ester (FAEE). This process reduced the severity of process parameters with high purity biodiesel yield. Process variables such as co-solvent ratio, ethanol to oil molar ratio, reaction temperature and reaction time were optimized. The maximum biodiesel yield of 88% was obtained at ethanol/oil molar ratio of 40:1, co-solvent (hexane) to oil ratio of 0.2% (v/v), reaction temperature of 300°C in 20 min of reaction time. Fatty acid ethyl ester (biodiesel) samples produced from this process were measured and evaluated using GC-MS analytical instrument. Thermo gravimetric analysis (TGA) was also performed to examine the thermal stability of waste cooking oil, ethyl esters and fuel blends. Fuel properties of ethyl esters were determined and compared with the ASTM standards for biodiesel, regular diesel and ethyl esters from different feedstock. 展开更多
关键词 FATTY Acid Ethyl ESTERS SUPERCRITICAL ETHANOLYSIS co-solvent Waste Cooking Oil
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Enhancement of Lipase-catalyzed Synthesis of Caffeic Acid Phenethyl Ester in Ionic Liquid with DMSO Co-solvent
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作者 顾双双 王俊 +3 位作者 魏贤彬 崔红生 吴向阳 吴福安 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2014年第Z1期1314-1321,共8页
Caffeic acid phenethyl ester(CAPE) is a natural and rare ingredient with several biological activities, but its industrial production using lipase-catalyzed esterification of caffeic acid(CA) and 2-phenylethanol(PE) i... Caffeic acid phenethyl ester(CAPE) is a natural and rare ingredient with several biological activities, but its industrial production using lipase-catalyzed esterification of caffeic acid(CA) and 2-phenylethanol(PE) in ionic liquids(ILs) is hindered by low substrate concentrations and long reaction time. To set up a high-efficiency bioprocess for production of CAPE, a novel dimethyl sulfoxide(DMSO)–IL co-solvent system was established in this study.The 2%(by volume) DMSO–[Bmim][Tf2N] system was found to be the best medium with higher substrate solubility and conversion of CA. Under the optimum conditions, the substrate concentration of CA was raised 8-fold,the reaction time was reduced by half, and the conversion reached 96.23%. The kinetics follows a ping-pong bi-bi mechanism with inhibition by PE, with kinetic parameters as follows: Vmax= 0.89 mmol · min-1· g-1, Km,CA=42.9 mmol · L-1, Km,PE= 165.7 mmol · L-1, and Ki,PE= 146.2 mmol · L-1. The results suggest that the DMSO cosolvent effect has great potential to enhance the enzymatic synthesis efficiency of CAPE in ILs. 展开更多
关键词 BIOCATALYSIS Caffeic acid phenethyl ESTER co-solvent Kinetics Ionic liquid
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Effects of Water-Soluble Co-Solvent on Properties of W/O Pickering Emulsions
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作者 张旭斌 谢世巍 +1 位作者 蔡旺锋 王富民 《Transactions of Tianjin University》 EI CAS 2016年第3期218-227,共10页
Effects of water-soluble co-solvents (WSCs)on the properties of water/oil Picketing emulsions were investigated. Picketing emulsions were prepared in the system of 1,2,4-trimethylbenzene (TMB)/hydrophobic sil- ica... Effects of water-soluble co-solvents (WSCs)on the properties of water/oil Picketing emulsions were investigated. Picketing emulsions were prepared in the system of 1,2,4-trimethylbenzene (TMB)/hydrophobic sil- ica/water with varied concentrations of WSCs (ethanol, acetic acid and glycerin). Mean droplet diameter distribu- tions of the obtained emulsions were studied to investigate the effects of WSCs types and concentrations. The results demonstrated that mean droplet diameter distributions decreased at first and then increased with the increase of WSC concentration. Moreover, the effect of WSC concentration on the phase inversion locus was further investi- gated. At the same time, infrared radiation (IR)spectrometer was used to investigate the mechanism. The results showed that the WSC attaching on hydrophobic silica changed the wettability of the particles, which facilitated the formation and phase inversion of the emulsion. The hydrogen bonds between the co-solvent groups attaching on the solid particles made a great effect on the droplet size of the emulsion and strengthened the interaction among emulsifiers. Overall, proper WSC was in favor of the stability of Picketing emulsion. 展开更多
关键词 Pickering emulsion water-soluble co-solvent mean droplet diameter distribution phase inversion locus
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Optimization of Biodiesel Production from Waste Vegetable Oil Assisted by Co-Solvent and Microwave Using a Two-Step Process
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作者 Chin-Chiuan Lin Ming-Chien Hsiao 《Journal of Sustainable Bioenergy Systems》 2013年第1期1-6,共6页
The two-step catalyzing process for biodiesel production from waste vegetable oil was assisted by both co-solvent and microwave irradiation. Central composite design (CCD) was employed to optimize the reaction conditi... The two-step catalyzing process for biodiesel production from waste vegetable oil was assisted by both co-solvent and microwave irradiation. Central composite design (CCD) was employed to optimize the reaction conditions. Optimal reaction conditions of the first step were alcohol to oil molar ratio of 9:1, catalyst (H2SO4) amount 1 wt%, reaction temperature 333 K, and reaction time 7.5 minutes;while for the second step, optimal reaction conditions were alcohol to oil molar ratio 12:1, catalyst (NaOH) amount 1 wt%, reaction temperature 333 K, and reaction time 2.0 minutes. The total reaction time was 9.5 min and the conversion rate of fatty acid methyl esters (FAMEs) achieved was 97.4%. The total reaction time was shorter than previous studies. Therefore, the co-solvent and microwave assisted two-step catalyzing process has a potential application in producing biodiesel from waste vegetable oil. 展开更多
关键词 WASTE VEGETABLE OIL co-solvent MICROWAVE TWO-STEP Process
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Fabricating low-temperature-tolerant and durable Zn-ion capacitors via modulation of co-solvent molecular interaction and cation solvation 被引量:8
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作者 Fuyun Li Le Yu +5 位作者 Qiaomei Hu Songtao Guo Yueni Mei Qing Liu Yapeng He Xianluo Hu 《Science China Materials》 SCIE EI CAS CSCD 2021年第7期1609-1620,共12页
Aqueous Zn-based energy-storage devices have aroused much interest in recent years.However,uncontrollable dendrite growth in the Zn anode significantly limits their cycle life.Moreover,the poor low-temperature perform... Aqueous Zn-based energy-storage devices have aroused much interest in recent years.However,uncontrollable dendrite growth in the Zn anode significantly limits their cycle life.Moreover,the poor low-temperature performance arising from the freezing of aqueous electrolytes at sub-zero temperatures restricts their practical applications in cold regions.Here,we fabricated low-temperature-tolerant and durable Zn-ion hybrid supercapacitors(ZHSCs)via modulating a co-solvent water/ethylene glycol electrolyte.The interaction of intermolecular hydrogen bonds between water and ethylene glycol as well as cation solvation was systematically investigated by tuning the co-solvent composition.The results illustrate that the ZnSO_(4)/water/ethylene glycol(65%)electrolyte possesses high ionic conductivity at low temperatures and effectively prevents the dendrite formation of the Zn anode.The as-fabricated ZHSCs exhibit long-term cyclability and are capable of working at sub-zero temperatures as low as -40℃.The present ZHSCs are anti-freezing and cost-effective,which may find new applications in the fields of next-generation electrochemical energy storage devices. 展开更多
关键词 low temperature co-solvent electrolyte Zn-ion capacitors ionic conductivity rational modulation
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Influence of co-solvent hydroxyl group number on properties of water-based conductive carbon pastes 被引量:3
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作者 Chengjie Hua Xiaoming Li +6 位作者 Lijuan Shen Hong Lei Xiaoqian Guo Zhuo Liu Qingqiang Kong Lijing Xie cheng-Meng Chen 《Particuology》 SCIE EI CAS CSCD 2017年第4期35-41,共7页
A series of water-based conductive carbon pastes were prepared by wet ball milling, followed by vacuum defoaming using isopropyl alcohol, propylene glycol or glycerin as co-solvents. Screen printing was then used to p... A series of water-based conductive carbon pastes were prepared by wet ball milling, followed by vacuum defoaming using isopropyl alcohol, propylene glycol or glycerin as co-solvents. Screen printing was then used to prepare conductive patterns. To determine the influence of co-solvent hydroxyl group number on the properties of water-based conductive carbon pastes, the rheological properties of the pastes and the surface morphologies and conductivities of the printed patterns were characterized. The results show that paste viscosity increased with the number of hydroxyl groups and the latter also affected thixotropy. In addition, the boiling points and surface tensions of the co-solvents increased consistently with hydroxyl group number, affecting the hydrodynamic flow. The conductive carbon paste created using propylene glycol as a co-solvent was the best for screen printing because of its weak coffee-ring effect and appro- priate rheological properties, resulting in a smooth coating surface and uniform deposition of the fillers. The resistivity of the pattern printed using paste PG, containing the closest packing of conductive carbon black particles, was 0.44 Ω cm. 展开更多
关键词 Water-based conductive carbon paste Alcohol co-solvent Screen printing Rheological property Marangoni flow
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基于静态溶蜡速率探究清防蜡药剂的影响因素
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作者 刘永卫 王鹏里 +4 位作者 刘松梅 赵浚凯 卢聪 吕雄伟 鱼涛 《石油化工应用》 2025年第7期100-104,共5页
石蜡是在原油开采过程中,随着原油在管线中上移的过程产生的,其会导致原油管线内径减小,造成管线堵塞,影响原油开采的正常运行,使用合理的药剂体系可以有效避免这一问题。为探究溶剂复配、表面活性剂和助溶剂种类及含量对溶蜡剂溶蜡速... 石蜡是在原油开采过程中,随着原油在管线中上移的过程产生的,其会导致原油管线内径减小,造成管线堵塞,影响原油开采的正常运行,使用合理的药剂体系可以有效避免这一问题。为探究溶剂复配、表面活性剂和助溶剂种类及含量对溶蜡剂溶蜡速率的影响。本研究复配了一种溶蜡剂主剂,并通过实验探究了表面活性剂和助溶剂对其溶蜡效果的影响。结果表明,当加入0.5%Span-80和8%正辛醇时,可使主剂溶蜡速率提高25.35%。本文研究成果对蜡沉积清理的理论研究和技术发展具有重要意义。 展开更多
关键词 溶蜡速率 表面活性剂 助溶剂
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[BMIM]Cl/共溶剂体系对临汾肥煤解聚性能的影响研究
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作者 谷俊玲 程亚楠 +3 位作者 王琳 王美君 常丽萍 孔娇 《现代化工》 北大核心 2025年第10期95-102,109,共9页
由于1-丁基-3-甲基咪唑氯盐([BMIM]Cl)解聚煤时存在粘度大、难分离的问题,为此向[BMIM]Cl中添加甲醇、N-甲基吡咯烷酮(NMP)、二甲基亚砜(DMSO)、N,N-二甲基甲酰胺(DMF)、水为共溶剂,研究[BMIM]Cl/共溶剂体系对浮沉酸洗后的临汾肥煤(LFS... 由于1-丁基-3-甲基咪唑氯盐([BMIM]Cl)解聚煤时存在粘度大、难分离的问题,为此向[BMIM]Cl中添加甲醇、N-甲基吡咯烷酮(NMP)、二甲基亚砜(DMSO)、N,N-二甲基甲酰胺(DMF)、水为共溶剂,研究[BMIM]Cl/共溶剂体系对浮沉酸洗后的临汾肥煤(LFS)解聚性能的影响。利用TG、FT-IR等分析手段对解聚产物及残煤的物理化学特性进行了系统表征。结果表明,相较于纯[BMIM]Cl,添加甲醇后,体系粘度降低,溶解性提高;解聚产物中GC×GC-MS可检测化合物增多,主要为2~5环芳烃化合物;对解聚产物的FT-ICR MS分析表明,其分子量主要分布在300~500 Da范围内,且以O_(x)类化合物为主,占比高达50.79%,可能为脂肪酸、1~5环的芳酚和芳酸等化合物。 展开更多
关键词 临汾肥煤 [BMIM]Cl 共溶剂 解聚性能 多环芳烃
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锆铪萃取分离体系溶液化学基础研究进展 被引量:1
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作者 吴明 吴净昀 +6 位作者 周多多 瞿军 何正艳 张臻悦 池汝安 王力军 徐志高 《稀有金属》 北大核心 2025年第6期949-961,共13页
核级锆(Zr)和核级铪(Hf)是保障核工业发展的重要基础材料。溶剂萃取分离是制备核级锆铪的技术关键。本文从溶液化学平衡角度,阐释了酸性介质有利于抑制锆铪离子的水解聚合,提高其反应活度。根据软硬酸碱理论和活性功能基差异,总结了近... 核级锆(Zr)和核级铪(Hf)是保障核工业发展的重要基础材料。溶剂萃取分离是制备核级锆铪的技术关键。本文从溶液化学平衡角度,阐释了酸性介质有利于抑制锆铪离子的水解聚合,提高其反应活度。根据软硬酸碱理论和活性功能基差异,总结了近年来研发的萃取剂主要有含O, N, P和S等不同类型,并评价了其主要优点和不足。结合有机膦酸类萃取剂的二聚体结构特征,阐述了具有电子给体特征的惰性有机溶剂对该类萃取剂的“解聚”作用机制。并且,从界面化学反应平衡角度,解释了具有一定溶解度的有机溶剂,对提升萃取反应效率的必要性。除此之外,还结合软硬酸碱理论和霍夫迈斯特序列,综述了锆铪溶剂萃取分离体系助萃剂、盐析剂和反萃剂等选用的基本原则,以期为锆铪高效溶剂萃取分离体系的研发和应用提供基础理论指导。 展开更多
关键词 锆(Zr) 铪(Hf) 溶剂萃取分离 助萃剂 盐析效应 反萃剂
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酸性共溶剂制备高长、羧基化汉麻纤维用于柔性导电传感
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作者 吕晓阳 刘源 +4 位作者 毕文静 曹磊 常德鹏 张显权 夏芹芹 《林业工程学报》 北大核心 2025年第3期86-93,共8页
汉麻纤维因其较高的力学强度、透气性、抑菌等优良性能被广泛用于纺织原料中。脱胶是从汉麻中直接提取纤维的必要步骤,但传统脱胶方法在低成本、绿色环保和高纤维质量等方面无法较好协调。本研究合成由氯化胆碱、柠檬酸和过氧化氢组成... 汉麻纤维因其较高的力学强度、透气性、抑菌等优良性能被广泛用于纺织原料中。脱胶是从汉麻中直接提取纤维的必要步骤,但传统脱胶方法在低成本、绿色环保和高纤维质量等方面无法较好协调。本研究合成由氯化胆碱、柠檬酸和过氧化氢组成的低成本、环保的酸性共溶剂,在温和条件下提取高长、高强、羧基化的汉麻纤维,并从脱胶效率、纤维素聚合度、羧基化程度等方面分析该酸性共溶剂的协同机理以及所制备的汉麻纤维的性能;进一步通过气相沉积技术,促使吡咯单体在汉麻纤维基底上进行聚合,成功合成柔性导电传感纤维材料。实验结果表明,该酸性共溶剂在80℃下对汉麻处理1 h后,木质素的脱除率高达86%,获得长达1 m、聚合度为2536、羧基化含量为0.30 mmol/g、拉伸强度为500 MPa的汉麻纤维;与碱处理相比,该体系更加温和高效,并在脱胶的同时实现对汉麻纤维的羧基化改性。此外,用该方法制备的汉麻纤维,其聚吡咯负载量可达43.85%,电导率为9.6 mS/m,在不同压力作用下电阻变化明显;与碱处理相比,聚吡咯负载量提高30%,导电性能显著提高31倍。研究结果证明该类绿色酸性共溶剂在温和条件下能够高效制备高质量纤维,并极大扩展了汉麻纤维在柔性织物导电传感方面的应用潜力。 展开更多
关键词 汉麻纤维 共溶剂 聚合度 羧基化 导电传感
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两嵌段共聚物在二元混合溶剂中的自组装:混致不溶效应的影响 被引量:1
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作者 李星业 王志远 +4 位作者 王铮 尹玉华 蒋润 张朋飞 李宝会 《高分子学报》 北大核心 2025年第8期1438-1448,共11页
采用模拟退火方法研究了AB两嵌段共聚物在二元混合溶剂中的自组装行为.考察了共聚物的体积分数、溶剂的性质及组成对自组装聚集体形态的影响,构建了聚集体形态随不同参量变化的相图,获得了多种不同形态的胶束,并揭示了聚集体的形成机制... 采用模拟退火方法研究了AB两嵌段共聚物在二元混合溶剂中的自组装行为.考察了共聚物的体积分数、溶剂的性质及组成对自组装聚集体形态的影响,构建了聚集体形态随不同参量变化的相图,获得了多种不同形态的胶束,并揭示了聚集体的形成机制.体系中两种溶剂(称为S和O)均为B嵌段的良溶剂,并且S溶剂对B嵌段的吸引作用强于O溶剂,S溶剂为A嵌段的不良溶剂.研究发现,当S溶剂的体积分数CS较小且A嵌段的体积分数fA较小,或者S溶剂与A嵌段间排斥作用较弱时,B嵌段的混致不溶效应起主导作用,共聚物主要形成以B嵌段为核、A嵌段为冠的胶束.胶束的核中有大量的S溶剂,并伴随着S溶剂的液液相分离现象.相反,当CS较大且S溶剂与A嵌段间排斥作用较强时,溶剂与A嵌段间的排斥作用起主导作用,共聚物主要形成以A嵌段为核、B嵌段为冠的胶束.当CS居间,或CS较小且fA较大时,上述两种作用的竞争导致共聚物形成多样化的补丁状、层状、聚集状和大蒜状等复杂胶束形态. 展开更多
关键词 模拟退火 两嵌段共聚物 混合溶剂 混致不溶 自组装
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均聚物在二元混合溶剂中的构象与聚集行为:粗粒化分子动力学模拟
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作者 王志远 李星业 +4 位作者 王铮 尹玉华 蒋润 张朋飞 李宝会 《高分子学报》 北大核心 2025年第10期1862-1872,共11页
刺激-响应型聚合物因能对外界环境变化(如温度、溶液组成等)产生可逆的物理或化学响应,而具有广泛的应用前景.这种响应可以表现为其链构象、溶解度等的变化.聚合物在混合溶剂中常表现出复杂的链构象和聚集行为,其中一个著名的例子是混... 刺激-响应型聚合物因能对外界环境变化(如温度、溶液组成等)产生可逆的物理或化学响应,而具有广泛的应用前景.这种响应可以表现为其链构象、溶解度等的变化.聚合物在混合溶剂中常表现出复杂的链构象和聚集行为,其中一个著名的例子是混致不溶(co-nonsolvency),即聚合物在由两种良溶剂混合组成的溶液中溶解度降低的现象.然而,目前关于混致不溶现象的物理机理仍存在很大争议.本文采用粗粒化分子动力学模拟,研究了均聚物单链和多链在混合溶剂中的链构象和聚集行为.结果表明,在混合溶剂中,多链体系中聚合物的链构象显著不同于与其对应的单链体系的链构象,随着共溶剂比例的增加,链呈现出分散-聚集-再分散的转变,意味着混致不溶效应的发生;同时,共溶剂呈现液-液相分离,高分子和共溶剂共同形成聚集体,构成共溶剂的浓相;并且,在聚集体内部的总粒子数密度大于体系的平均粒子数密度.此外,聚合物与共溶剂之间的相互作用强度对聚合物的径向密度分布有显著影响;随着该相互作用强度的变大,聚集体内部总粒子数密度逐渐增大.本研究揭示了混合溶剂中聚合物的微观结构的变化机制,并为理解聚合物在混合溶剂中的行为以及调控聚合物溶液的宏观性质提供理论依据. 展开更多
关键词 分子动力学模拟 混合溶剂 混致不溶 链构象 聚集行为
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羽毛微纤增强弹性纤维的绿色制备及传感性能研究
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作者 高天 郭志广 +2 位作者 刘吉东 吴军 刘新华 《安徽工程大学学报》 2025年第2期54-59,84,共7页
随着人工智能的快速发展,导电弹性纤维受到更多科研工作者的关注。然而,目前可拉伸导电纤维的绿色、高效制备及力学性能提升策略匮乏,这严重制约了其进一步应用。为此,本文基于氯化钙(CaCl_(2))-氯化胆碱-丙烯酸,设计了一种新型的可聚... 随着人工智能的快速发展,导电弹性纤维受到更多科研工作者的关注。然而,目前可拉伸导电纤维的绿色、高效制备及力学性能提升策略匮乏,这严重制约了其进一步应用。为此,本文基于氯化钙(CaCl_(2))-氯化胆碱-丙烯酸,设计了一种新型的可聚合低共熔溶剂体系(CaCl_(2)-PDES)用于绿色、高效地制备羽毛微纤力学增强弹性纤维。结果表明,CaCl_(2)-PDES溶剂体系不仅对羽毛具有可控溶解和剥离的作用,还可实现原位光聚合。当CaCl_(2)的浓度为2 wt.%,溶解温度为120℃时,羽毛能够被溶解为微米级(直径约为5μm)的蛋白质短纤,蛋白质短纤的存在增强了PAA-ChCl基弹性纤维的力学性能(断裂强度提升了1.7倍,0.62 MPa)。蛋白质微纤赋予纤维良好力学性能的同时,也保持了纤维良好的快速、灵敏的传感性能(拉伸、回复的反应时间分别为133 ms和172 ms,GF为0.78~1.44)。这项工作有效缓解了废弃生物质羽毛的高值化再利用的难题,同时为生物质弹性导电纤维的绿色制备提供了新的研究思路。 展开更多
关键词 羽毛 可聚合低共熔溶剂 离子导电弹性纤维 微纤增强
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油煤共炼馏分油制取环烷烃溶剂油
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作者 李晓宏 张轩 +2 位作者 汪亚斌 杜若宇 问王伟 《石化技术与应用》 2025年第4期280-283,292,共5页
对油煤共炼馏分油进行了加氢处理和馏分切割,得到了一系列环烷烃溶剂油,并考察了加氢处理过程中的反应条件对加氢处理产物分布、含硫(氮)量以及环烷烃溶剂油族组成的影响。结果表明:环烷烃溶剂油中的环烷烃质量分数受反应温度影响较大,... 对油煤共炼馏分油进行了加氢处理和馏分切割,得到了一系列环烷烃溶剂油,并考察了加氢处理过程中的反应条件对加氢处理产物分布、含硫(氮)量以及环烷烃溶剂油族组成的影响。结果表明:环烷烃溶剂油中的环烷烃质量分数受反应温度影响较大,其次为反应压力,最后为氢油体积比和体积空速;在反应温度370℃,反应压力18 MPa,氢油体积比1000,体积空速0.6 h^(-1)的条件下得到的环烷烃溶剂油的性质最优,其含硫量为3.81μg/g,含芳烃量为1.98μg/g,溴值(以100 g油计)为3.43 g/g,均满足我国3#低芳型溶剂油的标准要求。 展开更多
关键词 油煤共炼 加氢 溶剂油 环烷烃 含硫量 含氮量 芳烃
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CoS纳米片自支撑电极的制备及水分解性能
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作者 王庆典 孟艳芝 +4 位作者 李光振 邢苗苗 李晓茵 张德亮 牟红宇 《山东化工》 2025年第9期1-5,共5页
过渡金属硫化物因其独特的电子结构,被认为具有成为理想电解水催化剂的潜力。然而,其大都采用可溶性金属盐以及过量硫源作为前驱体,并通过液相和/或硫化技术来合成,合成过程比较繁琐且反应过程中会产生大量的含硫有毒化合物,不利于工业... 过渡金属硫化物因其独特的电子结构,被认为具有成为理想电解水催化剂的潜力。然而,其大都采用可溶性金属盐以及过量硫源作为前驱体,并通过液相和/或硫化技术来合成,合成过程比较繁琐且反应过程中会产生大量的含硫有毒化合物,不利于工业化生产且不符合绿色发展的要求。实验以溶有钴盐的绿色溶剂-低共熔溶剂(DESs)作为电解液,在碳布基底上采用简单的一步电沉积法制备CoS纳米片自支撑电极(CoS@CC)。制备的CoS为均匀生长在碳布表面的纳米片结构。研究表明:钴盐和硫脲的物质的量比例为1∶2、电沉积10圈时,当达到10 mA/cm^(2)的电流密度时,CoS@CC自支撑电极的析氢和析氧过电位仅为96和310 mV。此外,在全解水测试中,仅需要1.55 V的电压即可达到10 mA/cm^(2)的电流密度。 展开更多
关键词 CoS@CC 复合材料 催化剂 自支撑电极 低共熔溶剂 制氢
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An effective'salt in dimethyl sulfoxide/water'electrolyte enables high-voltage supercapacitor operated at-50℃ 被引量:1
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作者 Yingbin Liu Chang Yu +5 位作者 Xuedan Song Siyi Hou Shuqin Lan Jinhe Yu Yuanyang Xie Jieshan Qiu 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2024年第6期361-367,I0009,共8页
Compared with organic electrolytes,aqueous electrolytes exhibit significantly higher ionic conductivity and possess inherent safety features,showcasing unique advantages in supercapacitors.However,challenges remain fo... Compared with organic electrolytes,aqueous electrolytes exhibit significantly higher ionic conductivity and possess inherent safety features,showcasing unique advantages in supercapacitors.However,challenges remain for low-salt aqueous electrolytes operating at high voltage and low temperature.Herein,we report a low-salt(0.87 m,m means mol kg^(-1))'salt in dimethyl sulfoxide/water'hybrid electrolyte with non-flammability via hybridizing aqueous electrolyte with an organic co-solvent of dimethyl sulfoxide(hydrogen bond acceptor).As a result,the 0.87 m hybrid electrolyte exhibits enhanced electrochemical stability,a freezing temperature below-50℃,and an outstanding ionic conductivity of 0.52mS cm~(-1)at-50℃.Dimethyl sulfoxide can anchor water molecules through intermolecular hydrogen bond interaction,effectively reinforcing the stability of water in the hybrid electrolyte.Furthermore,the interaction between dimethyl sulfoxide and water molecules diminishes the involvement of water in the generation of ordered ice crystals,finally facilitating the low-temperature performance of the hybrid electrolyte.When paired with the 0.87 m'salt in dimethyl sulfoxide/water'hybrid electrolyte,the symmetric supercapacitor presents a 2.0 V high operating voltage at 25℃,and can operate stably at-50℃.Importantly,the suppressed electrochemical reaction of water at-50℃further leads to the symmetric supercapacitor operated at a higher voltage of 2.6 V.This modification strategy opens an effective avenue to develop low-salt electrolytes for high-voltage and low-temperature aqueous supercapacitors. 展开更多
关键词 Dimethyl sulfoxide co-solvent High voltage Low temperature SUPERCAPACITORS
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