首页> 美国卫生研究院文献>Polymers >Development of Polymeric Membranes Based on Quaternized Polysulfones for AMFC Applications
【2h】

Development of Polymeric Membranes Based on Quaternized Polysulfones for AMFC Applications

机译:基于季铵化聚砜的AMFC应用聚合物膜的开发

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

A series of quaternary ammonium-functionalized polysulfones were successfully synthesized using a chloromethylation two-step method. In particular, triethylammonium and trimethylammonium polysulfone derivatives with different functionalization degrees from 60% to 150% were investigated. NMR spectroscopic techniques were used to determine the degree of functionalization of the polymers. The possibility to predict the functionalization degree by a reaction tool based on a linear regression was highlighted. Anionic membranes with a good homogeneity of thickness were prepared using a doctor-blade casting method of functionalized polymers. The chemical–physical data showed that ion exchange capacity, water content, and wettability increase with the increase of functionalization degree. A higher wettability was found for membranes prepared by the trimethylamine (TMA) quaternary ammonium group. A degree of functionalization of 100% was chosen for an electrochemical test as the best compromise between chemical–physical properties and mechanical stability. From anionic conductivity measurement a better stability was found for the triethylamine (TEA)-based membrane due to a lower swelling effect. A power density of about 300 mW/cm for the TEA-based sample at 60 °C in a H /O fuel cell was found.
机译:使用氯甲基化两步法成功地合成了一系列季铵官能化的聚砜。特别地,研究了具有60%至150%的不同官能化度的三乙铵和三甲铵聚砜衍生物。 NMR光谱技术用于确定聚合物的官能化程度。强调了基于线性回归通过反应工具预测功能化程度的可能性。使用功能化聚合物的刮刀流延法制备具有良好厚度均匀性的阴离子膜。化学-物理数据表明,离子交换能力,水含量和润湿性随功能化程度的增加而增加。发现由三甲胺(TMA)季铵基制备的膜具有更高的润湿性。电化学测试选择100%的官能度作为化学-物理性质和机械稳定性之间的最佳折衷。从阴离子电导率测量中,由于较低的溶胀作用,发现基于三乙胺(TEA)的膜具有更好的稳定性。发现在60°C的H / O燃料电池中,基于TEA的样品的功率密度约为300 mW / cm。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号