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磺化芳香聚合物与其他聚合物共混制备复合膜是改善磺化芳香聚合物质子交换膜性能的一种有效方法。就最近几年来碱性聚合物及其他聚合物与磺化芳香聚合物复合的研究现状进行了分析,对其中存在的问题进行了阐述。 相似文献
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Seansoo Hwang HyeonGyeong Lee Yu-Gyeong Jeong Chanhee Choi Inhyeok Hwang SeungHyeon Song Sang Yong Nam Jin Hong Lee Kihyun Kim 《International journal of molecular sciences》2022,23(22)
To mitigate the dependence on fossil fuels and the associated global warming issues, numerous studies have focused on the development of eco-friendly energy conversion devices such as polymer electrolyte membrane fuel cells (PEMFCs) that directly convert chemical energy into electrical energy. As one of the key components in PEMFCs, polymer electrolyte membranes (PEMs) should have high proton conductivity and outstanding physicochemical stability during operation. Although the perfluorinated sulfonic acid (PFSA)-based PEMs and some of the hydrocarbon-based PEMs composed of rationally designed polymer structures are found to meet these criteria, there is an ongoing and pressing need to improve and fine-tune these further, to be useful in practical PEMFC operation. Incorporation of organic/inorganic fillers into the polymer matrix is one of the methods shown to be effective for controlling target PEM properties including thermal stability, mechanical properties, and physical stability, as well as proton conductivity. Functionalization of organic/inorganic fillers is critical to optimize the filler efficiency and dispersion, thus resulting in significant improvements to PEM properties. This review focused on the structural engineering of functionalized carbon and silica-based fillers and comparisons of the resulting PEM properties. Newly constructed composite membranes were compared to composite membrane containing non-functionalized fillers or pure polymer matrix membrane without fillers. 相似文献
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《国际聚合物材料杂志》2012,61(13):683-689
Hexagonal boron nitride (h-BN) particles have attracted increasing interest due to mechanical properties, chemical stability, electrical features, thermal stability, and good lubrication property. In this work hexagonal boron nitride were used as inorganic fillers, which increase the mechanical and thermal stabilities of the membrane. The proton conducting polymer membranes were prepared by blending of sulfonated polysulfone, polyvinyl phosphonic acid, and boron nitride. Scanning electron microscopy indicated the homogeneous distribution of hBN nanoparticles in the polymer matrix. hBN increased the proton conductivity and in the anhydrous state the maximum proton conductivity was determined as 7.9 × 10?3 S/cm at 150°C for PVPA-SPSU-5hBN. 相似文献
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Mohammad Ebrahimi Wojciech Kujawski Kateryna Fatyeyeva Joanna Kujawa 《International journal of molecular sciences》2021,22(11)
Today, the use of polymer electrolyte membranes (PEMs) possessing ionic liquids (ILs) in middle and high temperature polymer electrolyte membrane fuel cells (MT-PEMFCs and HT-PEMFCs) have been increased. ILs are the organic salts, and they are typically liquid at the temperature lower than 100 °C with high conductivity and thermal stability. The membranes containing ILs can conduct protons through the PEMs at elevated temperatures (more than 80 °C), unlike the Nafion-based membranes. A wide range of ILs have been identified, including chiral ILs, bio-ILs, basic ILs, energetic ILs, metallic ILs, and neutral ILs, that, from among them, functionalized ionic liquids (FILs) include a lot of ion exchange groups in their structure that improve and accelerate proton conduction through the polymeric membrane. In spite of positive features of using ILs, the leaching of ILs from the membranes during the operation of fuel cell is the main downside of these organic salts, which leads to reducing the performance of the membranes; however, there are some ways to diminish leaching from the membranes. The aim of this review is to provide an overview of these issues by evaluating key studies that have been undertaken in the last years in order to present objective and comprehensive updated information that presents the progress that has been made in this field. Significant information regarding the utilization of ILs in MT-PEMFCs and HT-PEMFCs, ILs structure, properties, and synthesis is given. Moreover, leaching of ILs as a challenging demerit and the possible methods to tackle this problem are approached in this paper. The present review will be of interest to chemists, electrochemists, environmentalists, and any other researchers working on sustainable energy production field. 相似文献
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采用相转化法制备了磺化聚砜(SPSF)/聚醚砜(PES)共混新型纳滤膜,并研究了SPSF/PES共混质量比、水解的苯乙烯–马来酸酐共聚物(H–PSMA)的添加量、铸膜液预蒸发时间和温度对膜的脱盐率及水通量的影响。结果表明,当SPSF/PES共混质量比为4∶6,添加剂H–PSMA的质量分数为2%,铸膜液预蒸发时间为3 min,预蒸发温度为70℃时,在操作压力为0.5 MPa,料液温度为25℃下,SPSF/PES共混膜对2 g/L的Na_2SO_4盐溶液脱盐率为56.77%,水通量为24.45 L/(m~2·h)。 相似文献
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A novel phenomenon of mechanoelectrical conversion in a flexible solid‐state polymer electrolyte membrane (PEM) is presented, hereafter denoted as flexoelectric effect. The flexoelectric coefficient (≈323 µC m?1), that is, a measure of the converted mechanoelectrical energy, is the highest among all flexoelectric materials hitherto reported. It is proposed in this work that the flexoelectricity in PEMs operates based on electrical energy generation driven by ion polarization/depolarization across the PEM subjected to a pressure gradient during bending. Of particular interest is the phenomenon of polarity switching during bending, that is, reversal of the polarization direction with increasing succinonitrile (SCN) concentration (i.e., 10–20 wt%). The size disparity between the solvated cations and anions is attributed as the key factor in determining the polarization direction, which is responsible for the polarity switching. Of particular importance is that the present flexoelectric PEM itself is a key component of the solid‐state lithium ion battery and thus their integration opens up a new avenue for energy harvesting and storage devices. 相似文献
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辐照改性聚丙烯抗熔垂能力的研究 总被引:1,自引:0,他引:1
采用熔垂测试仪测量了不同配方辐照改性聚丙烯(PP)的抗熔垂能力,分析了温度、敏化剂含量、辐照剂量和高相对分子质量物质等因素对PP抗熔垂能力的影响,提出了PP辐照过程中长支链的形成机理,解释了PP抗熔垂能力随辐照剂量变化的规律。结果表明,辐照改性能显著提高PP的抗熔垂能力,PP的抗熔垂能力随温度的升高而降低,并随敏化剂含量的增加而提高,在辐照过程中加入极少量高相对分子质量物质能有效提高PP的抗熔垂能力;辐照改性的PP可在较宽的温度范围内表现出较强的抗熔垂能力,有利于发泡、热成型等。 相似文献
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A sulfonated poly(ether ether ketone) (SPEEK) membrane with fairly high degree of sulfonation (DS) swells excessively and even dissolves at high temperature. To solve these problems, sulfonated phenolphthalein poly(ether sulfone) (SPES-C, DS 53.7%) is blended with the SPEEK matrix (DS 55.1%, 61.7%) to prepare SPEEK/SPES-C blend membrane. The decrease in swelling degree and methanol permeability of the membrane is dose-dependent. Pure SPEEK (DS 61.7%) membrane dissolves completely in water at 70ºC, whereas the swelling degree of the SPEEK (DS 61.7%)/SPES-C (40%, by mass) membrane is 29.7% at 80ºC. From room temperature to 80ºC, the methanol permeability of all SPEEK (DS 55.1%)/SPES-C blend membranes is about one order of magnitude lower than that of Nafion®115. At higher temperature, the addition of SPES-C polymer increases the dimensional stability and greater proton conductivity can be achieved. The SPEEK (DS 55.1%)/SPES-C (40%, by mass) membrane can withstand temperatures up to 150ºC. The proton conductivity of SPEEK (DS 55.1%)/SPES-C (30%, by mass) membrane approaches 0.16 S8226;cm-1, matching that of Nafion61650;115 at 140ºC and 100% RH, while pure SPEEK (DS 55.1%) membrane dissolves at 90ºC. The SPEEK/SPES-C blend membranes are promising for use in direct methanol fuel cells because of their good dimensional stability, high proton conductivity, and low methanol permeability. 相似文献
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Polyethersulfone was sulfonated by heterogeneous method with chlorosulfonic acid. Ion exchange capacity was controlled to 0.68 meq/g to reduce fouling. Sulfonation was confirmed by Fourier transform infrared spectroscopy and 1H‐nuclear magnetic resonance. Polyethersulfone and sulfonated polyethersulfone ultrafiltration membranes were prepared successively by the typical phase inversion method. Membrane performance of sulfonated polyethersulfone was compared with that of polyethersulfone. In the preparation of ultrafiltration membranes, the effect of the addition of dichloromethane and poly(vinyl pyrrolidone) in a casting solution was investigated on the membrane performance. It was observed that the addition of dichloromethane increased the solute rejection rate. By changing the ratio between polymer and poly(vinyl pyrrolidone), membrane performance could be controlled. Negatively charged sulfonated polyethersulfone could reduce fouling at higher or lower pH than isoelectric point of protein bovine serum albumin. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 2046–2055, 1999 相似文献
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利用静电纺丝技术制备了聚吲哚/聚丙烯腈(PIN/PAN)聚合物基电解质膜,代替纸基铝空气电池中的纤维素纸(C-P),并应用于固态铝空气电池。探究了PIN含量对电解质膜离子电导率及吸液率的影响。采用SEM和FTIR对PIN/PAN聚合物基电解质膜表面形貌及化学组成进行分析。借助电化学工作站和电池测试系统,分析了电解质膜离子电导率及固态铝空气电池放电特性。结果表明,采用PIN/PAN聚合物基电解质膜可有效提升固态铝空气电池性能,在3 mA.cm-2、5 mA.cm-2、7 mA.cm-2电流密度下,放电时长比纸基铝空气电池分别提升了21%、27%、34%,且放电时长与电解质膜的吸液率及离子电导率相关。其中4%PIN/PAN聚合物基电解质膜离子电导率可达6.7×10-4 S.cm-1,同时对碱性溶液具有良好的吸附能力,吸液率最高可达496%,为纤维素纸的3.2倍。 相似文献
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In this paper, the effect of hydrogen reduction of silver ions on the performance and structure of new solid polymer electrolyte polyetherimide (PEI)/Pebax2533 (Polynylon12/tetramethylene oxide block copolymer, PA12-PTMO)/AgBF4 composite membranes is investigated. For PEI/Pebax2533/AgBF4 composite membranes prepared with different AgBF4 concentration, the permeances of propylene and ethylene increase with the increase of AgBF4 concentration due to the carrier-facilitated transport, resulting in a high selectivity. But for propylene/propane mixture, the mixed-gas selectivity is lower than its ideal selectivity. The hydrogen reduction strongly influences the membrane performance, which causes the decrease of propylene permeance and the increase of propane permeance. With the increase of hydrogen reduction time, the membranes show a clearly color change from white to brown, yielding a great selectivity loss. The data of X-ray diffraction and FT-IR prove that silver ions are reduced to Ag0 after hydrogen reduction, and aggregated on the surface of PEI/Pebax2533/AgBF4 composite membranes. 相似文献
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水溶性交联聚合物微球的制备及性能 总被引:18,自引:1,他引:18
采用反相微乳液聚合制备水溶性交联聚合物微球。交联比为0 1%、0 5%、1 0%时,微球平均粒径分别为74 9、151 8、214 9nm。水化时间由0增至144h时,微球平均粒径由106 7nm增大到189 5nm。盐质量分数由0增至0 5%时,微球平均粒径由202 7nm减小到93 5nm。微孔滤膜封堵性能随水化时间无明显变化,随盐质量分数的增加而明显降低。岩心封堵实验表明,交联聚合物微球对气测渗透率为3 058μm2的岩心的流动阻力可达120kPa。 相似文献
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