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环境水样中全氟磺酸类和全氟羧酸类化合物分析方法研究进展 被引量:5
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作者 吴建刚 龙强 +3 位作者 肖文 黄博珠 赵金平 向运荣 《环境化学》 CAS CSCD 北大核心 2018年第8期1851-1859,共9页
全氟化合物(PFCs)作为一类难降解的持久性污染物,由于其可能导致肝毒性、致癌性、免疫毒性、生殖毒性以及干扰内分泌等特性,近年来成为研究的热点.通常环境水样中PFCs含量较低,其中全氟磺酸类化合物(PFSAs)和全氟羧酸类化合物(PFCAs)为... 全氟化合物(PFCs)作为一类难降解的持久性污染物,由于其可能导致肝毒性、致癌性、免疫毒性、生殖毒性以及干扰内分泌等特性,近年来成为研究的热点.通常环境水样中PFCs含量较低,其中全氟磺酸类化合物(PFSAs)和全氟羧酸类化合物(PFCAs)为痕量水平,因此环境水样中PFSAs和PFCAs的分析需要建立灵敏可靠的分析方法.国内外已针对环境水样中PFSAs和PFCAs的分析开展了大量研究,但全面系统的评述其分析方法近年来的新进展鲜见报道.本文全面总结了近5年来环境水样中PFSAs和PFCAs前处理方法及检测技术的新进展,主要包含基于色谱质谱的分析方法、基于光谱的分析方法、基于酶联免疫吸附测定(ELISA)的分析方法等三类;重点对样品前处理方法和检测技术的新进展进行综述;并对各种方法的优缺点进行了比较和评述.在此基础上对其发展趋势进行展望,以期为相关研究提供参考. 展开更多
关键词 环境水样 pfsas和PFCAs 检测方法 前处理方法 进展
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全氟表面活性剂对电极反应的影响─—非离子型全氟表面活性剂与碳氢链表面活性剂的比较 被引量:1
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作者 祖延兵 颜佳伟 《材料保护》 CAS CSCD 北大核心 1997年第12期8-10,共3页
研究了非离子型全氟表面活性剂在汞电极表面的吸附行为及对若干典型电还原反应的影响,并与相应的碳氢链表面活性剂作了比较。结果表明,在零电荷电位附近,两类表面活性剂均以憎水链吸附于电极表面,由于全氟链的吸附活性弱于碳氢链,... 研究了非离子型全氟表面活性剂在汞电极表面的吸附行为及对若干典型电还原反应的影响,并与相应的碳氢链表面活性剂作了比较。结果表明,在零电荷电位附近,两类表面活性剂均以憎水链吸附于电极表面,由于全氟链的吸附活性弱于碳氢链,其对电极表面的屏蔽作用及对电极反应的阻碍均较弱。在负极化区,憎水链脱附,亲水基团吸附于电极表面,这时两类表面活性剂对电极反应的阻碍作用一般相差不大。 展开更多
关键词 电极反应 非离子型 表面活性剂 CHSAS pfsas
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PVA-PFSA/PAN渗透汽化膜强化乙酸乙酯酯化脱水及工艺过程模拟 被引量:2
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作者 袁海宽 许振良 +3 位作者 马晓华 魏永明 齐峻 曾义红 《华东理工大学学报(自然科学版)》 CAS CSCD 北大核心 2009年第2期174-179,共6页
以聚丙烯腈(PAN)中空纤维超滤膜为底膜,以酒石酸(Tac)为交联剂,制备了聚乙烯醇(PVA)与全氟磺酸(PFSA)共混复合膜,并用于乙酸乙酯-水、乙酸乙酯-乙醇-水溶液的脱水研究。考察了分离乙酸乙酯-水二元溶液时,料液温度和含水量对复合膜分离... 以聚丙烯腈(PAN)中空纤维超滤膜为底膜,以酒石酸(Tac)为交联剂,制备了聚乙烯醇(PVA)与全氟磺酸(PFSA)共混复合膜,并用于乙酸乙酯-水、乙酸乙酯-乙醇-水溶液的脱水研究。考察了分离乙酸乙酯-水二元溶液时,料液温度和含水量对复合膜分离性能的影响;40℃下分离含水2%(质量分数,下同)的乙酸乙酯水溶液时,其总渗透通量81.1 g/(m2.h),分离因子为1 890;考察了复合膜用于分离乙酸乙酯-乙醇-水(质量比90∶2∶8)三元溶液时,料液温度的影响及脱水效果。结果表明:40℃时复合膜对三元溶液的总渗透通量可达251.0 g/(m2.h),此温度下,只需12 h就可将含8%初始水的三元溶液脱水至4.66%。PVA-PFSA/PAN渗透汽化膜对乙酸乙酯体系的脱水效果良好,可应用于强化乙酸乙酯酯化生产工艺。利用Aspen Plus 11.1软件对工艺流程进行了模拟,结果表明:在同等操作条件下,渗透汽化膜强化酯化工艺流程相对于普通的反应精馏,提高了乙酸乙酯的单程收率和原料的转化率,简化了乙酸乙酯生产流程。 展开更多
关键词 聚乙烯醇(PVA) 全氟磺酸(PFSA) 渗透汽化 强化酯化 模拟
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燃料电池用WO_3/PFSA复合膜的制备及研究
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作者 杨金燕 魏小兰 《电池工业》 CAS 2010年第3期142-146,共5页
用具有溢氢效应的三氧化钨(WO3)对全氟磺酸聚合物电解质膜(PFSA)改性,制备了一系列WO3/PFSA复合膜。对制备的复合膜进行扫描电镜(SEM)、能谱(EDX)测试,结果表明复合膜的表面均匀而致密,W元素分布在整个膜中。热重实验表明复合膜的热稳... 用具有溢氢效应的三氧化钨(WO3)对全氟磺酸聚合物电解质膜(PFSA)改性,制备了一系列WO3/PFSA复合膜。对制备的复合膜进行扫描电镜(SEM)、能谱(EDX)测试,结果表明复合膜的表面均匀而致密,W元素分布在整个膜中。热重实验表明复合膜的热稳定性能提高了。复合膜具有明显的阻醇作用,并随膜中WO3含量的增加阻醇性能增强。质子电导率的测试结果表明,在非极化状态下复合膜的质子电导率和Nafion誖112膜相比有所降低。 展开更多
关键词 直接甲醇燃料电池 WO3 PFSA膜 甲醇渗透率 质子电导率
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Miscibility on blends of PVA and PFSA by viscometry
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作者 郎万中 许振良 +2 位作者 郭亚军 褚联峰 童蔚 《Journal of Shanghai University(English Edition)》 CAS 2009年第3期260-262,共3页
The intrinsic viscosity and viscometric interaction parameters of perfluorosulfonic acid (PFSA) and poly(vinyl alcohol) (PVA) were measured by dilute solution viscometry. The miscibility between PFSA and PVA was... The intrinsic viscosity and viscometric interaction parameters of perfluorosulfonic acid (PFSA) and poly(vinyl alcohol) (PVA) were measured by dilute solution viscometry. The miscibility between PFSA and PVA was estimated by the criteria of AB and μ. The results indicated that PFSA and PVA were completely miscible for any weight fraction in aqueous solution. 展开更多
关键词 MISCIBILITY dilute solution viscometry perfluorosulfonic acid (PFSA) poly(vinyl alcohol)(PVA)
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氮气吸附等温线分析PFSA/SiO2复合催化剂孔结构 被引量:5
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作者 袁海宽 马晓华 许振良 《中国科学:化学》 CAS CSCD 北大核心 2011年第6期1094-1094,共1页
采用溶胶-凝胶法制备了全氟磺酸/二氧化硅(PFSA/SiO2)复合催化剂.调整PFSA与TEOS的配比,可制得不同PFSA负载量的复合催化剂.将PFSA含量分别为5%,13%,20%和40%的催化剂记为PFSA-5,PFSA-13,PFSA-20和PFSA-40.四种催化剂的等温线均属于Ⅳ... 采用溶胶-凝胶法制备了全氟磺酸/二氧化硅(PFSA/SiO2)复合催化剂.调整PFSA与TEOS的配比,可制得不同PFSA负载量的复合催化剂.将PFSA含量分别为5%,13%,20%和40%的催化剂记为PFSA-5,PFSA-13,PFSA-20和PFSA-40.四种催化剂的等温线均属于Ⅳ型等温线,PFSA-5,PFSA-13和PFSA-20催化剂属H1型滞后环,而PFSA-40催化剂属H2型滞后环.采用BET法确定比表面积,BJH法计算孔径分布.结果显示,在PFSA/SiO2催化剂内形成了较为发达的圆柱状中孔,且分布较为均一.随着催化剂内PFSA负载量的增大,表面积和孔容逐渐减小.PFSA-40催化剂的表面积和孔容急剧降低,主要是由于过多的PFSA负载量使SiO2孔网络的连续性受到破坏,或部分孔道被堵塞所造成的.总的来说,高度分散和多孔的结构使催化剂的比表面积增大,提高了活性中心的可接近程度,同时也降低催化剂的成本.中孔材料的吸附脱附等温线中存在吸附滞后,滞后环的形状反映了孔结构类型.PFSA-5,PFSA-13和PFSA-20催化剂的吸附滞后环属于H1型,一般由大小均一且形状规则的孔造成.而PFSA-40催化剂的滞后环变成了H2型,催化剂内形成具有瓶颈状的圆柱状孔,且分布不均一.采用对比曲线法(t曲线)可修正由BJH方法得到的PFSA/SiO2催化剂的孔径分布.PFSA-5,PFSA-13和PFSA-20催化剂的t曲线有三个阶段构成,分别命名为Stage A,StageB,Stage C.Stage A,孔壁内N2多层吸附;StageC,N2外表面吸附;StageB中,PFSA-5,PFSA-13和PFSA-20催化剂的t曲线非常陡,表明孔内毛细管凝聚的发生,同时也预示中孔结构形成.PFSA-40催化剂的t曲线StageB的水平偏离表明其内有微孔存在,即PFSA-40催化剂内部并不是分布均一的中孔,这与氮气吸附滞后的分析结果相一致.另外,t曲线的微分形状与多孔材料的孔径分布非常相似,能定性反映PFSA/SiO2催化剂的孔径分布.PFSA-5,PFSA-13和PFSA-20催化剂的微分曲线在t=0.6~1.0nm存在较为尖锐的峰,意味着均一孔结构的形成.PFSA-40催化剂的微分曲线上所形成的峰并不明显,表明PFSA-40催化剂具有较宽的孔径分布,与吸附滞后的分析结果一致.因此,使用t曲线及其微分曲线来分析PFSA/SiO2催化剂的孔径分布是对BJH法很好的补充. 展开更多
关键词 孔结构 PFSA/SiO2复合催化剂 吸附-脱附等温线 吸附滞后 t曲线
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Preparation of PFSA/PSf hollow fiber composite membranes with recovered PFSA for the pervaporation separation of EtOH/H_2O 被引量:1
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作者 LANG WanZhong1,2,TONG Wei2,XU ZhenLiang2 & GUO YaJun1 1Department of Chemistry,Shanghai Normal University,Shanghai 200234,China 2Chemical Engineering Research Center,East China University of Science and Technology,Shanghai 200237,China 《Science China Chemistry》 SCIE EI CAS 2010年第1期273-280,共8页
Perfluorosulfonic acid/Polysulfone(PFSA/PSf) hollow fiber composite membranes have been prepared by dip-coating method using PSf ultrafiltration(UF) membrane as substrate with recovered PFSA.The composite membranes we... Perfluorosulfonic acid/Polysulfone(PFSA/PSf) hollow fiber composite membranes have been prepared by dip-coating method using PSf ultrafiltration(UF) membrane as substrate with recovered PFSA.The composite membranes were applied to the pervaporation separation of 95% ethanol(EtOH)/H2O mixture.SEM images show that the thickness of the PFSA skin layer of the composite membranes is about 2 μm,much thinner than those of other PFSA composite membranes revealed in the literatures.Effects of annealing temperature,coating solution concentration and counter-ions of PFSA on the pervaporation performances of the composite membranes were investigated.The total flux decreases and separation factor increases with the increase of annealing temperature.The highest permeation flux of 3230 g m-2 h-1 and a separation factor of 5.4 is obtained for the composite membrane annealed at 80°C.The lowest permeation flux of 396 g m-2 h-1 and a separation factor of 27.7 is obtained for the composite membrane annealed at 160°C.The permeation performances of the PFSA/PSf composite membrane are evidently influenced by the counter-ions of PFSA.The flux sequence of the PFSA/PSf composite membranes with different counter-ions is H+>Li+>Ca2+>Mg2+>Na+>K+>Ba2+>Fe3+>Al3+,and the separation factor sequence is H+<Li+<Al3+<Na+<Mg2+<Ca2+<K+ <Ba2+<Fe3+.The apparent activation energy △Eapp values of the composite membranes with different counter-ions were calculated by Arrhenius law.The sequence of △Eapp values for the membranes with monovalent counter-ions is Li+>Na+>K+.There are very little variations of △Eapp values between the composite membranes with three divalent counterions(Mg2+,Ca2+ and Ba2+),and the △Eapp values of the composite membranes with two trivalent counterions(Fe3+ and Al3+) are relatively high. 展开更多
关键词 PERVAPORATION HOLLOW fiber composite membrane perfluorslulfonic acid(PFSA) ethanol(EtOH)/H2O MIXTURE
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Formulation of carbon black-ionomer dispersions for thin film formation in fuel cells
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作者 Eva Hoffmann Su Zhang +2 位作者 Martin Thoma Cornelia Damm Wolfgang Peukert 《Particuology》 SCIE EI CAS CSCD 2019年第3期7-21,共15页
The performance of proton exchange membrane fuel cells (PEMFC) is strongly determined by the structure and composition of the electrode layer.The interactions between the ionomer,carbon black particles,and solvent aff... The performance of proton exchange membrane fuel cells (PEMFC) is strongly determined by the structure and composition of the electrode layer.The interactions between the ionomer,carbon black particles,and solvent affect the suspension properties and thus the layer morphology.We analyze the effect of the ionomer-to-carbon (I/C) weight ratio for two different types of carbon black on the suspension and layer characteristics.Highly branched carbon blacks with a high surface area tend to form less cracked layers.As less branched carbons can pack together more closely,a smaller pore size results in a larger capillary pressure during drying and thus more cracks.The added ionomer adsorbs on the carbon particles and improves the colloidal stability of the carbon black particles.The carbon black aggregates are thus smaller,resulting in closer packing and thinner layers.Moreover,the addition of the ionomer increases the critical coating thickness (CCT) of the layers because drying stresses are dissipated by the deformation of the ionomer,preventing crack formation.An optimum I/C weight ratio is identified for optimal layer formation and minimized crack formation. 展开更多
关键词 Perfluorosulfonic acid (PFSA) IONOMER Carbon black Layer FORMATION CRACKING POROSITY
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Probe Staurosporine Drug Binding Site on Protein Kinase by PFSC
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作者 ZHENG Kun YANG Hong +3 位作者 ZHAO Xiaofei JIANG Yang SUN Chuantao YANG Jia'an 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2014年第4期644-649,共6页
We used a new approach,protein folding shape code(PFSC),to predict the potential staurosporine binding sites in protein kinases.Firstly,all available three dimensioned(3D) structures of protein kinases in protein ... We used a new approach,protein folding shape code(PFSC),to predict the potential staurosporine binding sites in protein kinases.Firstly,all available three dimensioned(3D) structures of protein kinases in protein databank(PDB) were converted into one-dimensional PFSC description,based on which a PFSC-kinome library was constructed.Secondly,a set of protein kinase-staurosporine complexes were analyzed to define the common structural features of the binding sites.Thirdly,the structural features of the staurosporine binding sites were used to virtually screen the PFSC-kinome library to predict multiple protein receptors that have potential binding capacity for staurosporine.Collectively,the development of the similar method for predicting drug binding site demonstrates that virtual screening protein database can provide valuable information on drug discovery and understanding of pharmacological pathways. 展开更多
关键词 STAUROSPORINE Adenosine triphosphate(ATP)-binding site Protein fold shape code(PFSC) Protein folding structural alignment(PFSA) Protein databank(PDB)
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