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Enhanced hiqh-temperature polymer electrolyte membrane for fuel cells based on 1H- 1,2,3-benzotriazole and sulfonated poly(vinyl alcohol)

机译:基于1H-1,2,3-苯并三唑和磺化聚(乙烯醇)的燃料电池增强的HiQH-温度聚合物电解质电解质膜

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Fuel cells based on polymer electrolyte membranes have been widely studied during the last four decades due to their promising high energy conversion efficiency, their high energy density power sources for both automobiles and stationary applications. The development of anhydrous proton conducting membrane is important for the operation of polymer electrolyte membrane fuel cell (PEMFC) at intermediate temperature (100-200 °C). Therefore, there has been a great deal of research in the development of anhydrous electrolyte membranes with high proton conductivities at higher temperatures [1-4]. One approach was the use of nitrogen-containing aromatic heterocycles molecules -with boiling points higher than water- as proton carriers, either as doping agents or immobilized in the polymer backbone, originating polymers with intrinsic proton conductivity. 1H-1,2,3-benzotriazole (BTri) is a novel heterocyclic molecule with melting and boiling points of 100 and 350 °C, respectively. Previously it was used as dopant in polyvinyl phosphonic acid and Nation and high proton conductivity (10~3 S/cm at 150 °C) was reported [5]. In this study, we have prepared the acid-base composite materials by mixing of a sulfonated poly(vinyl alcohol) (PVA) with the high proton exchange capacity and an organic base heterocycle, 1 H-1,2,3-benzotriazole. Sulfonic acid groups were introduced into PVA matrix at various molar ratios by modifying the chemical structure of the PVA through esterification with sulfosuccinic acid (SSA), which has sulfonic acid groups. The resulting cross linked polymer was blended with 1 H-1,2,3-benzotriazole at several molar ratios (Table 1) to obtain a matrix that has acid groups immobilized into the chain and azoles interacting with the acid groups in the matrix. The polymers were characterized with Fourier transform infrared (FT-IR), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). The proton conductivity of the anhydrous samples was studied by an impedance spectrometer, and the results are compared with the previously reported systems.
机译:基于聚合物电解质膜的燃料电池由于其具有高能量转换效率,其高能量密度电源,用于汽车和静止应用而被广泛研究了最近四十年。无水质子传导膜的开发对于在中间温度(100-200℃)下聚合物电解质膜燃料电池(PEMFC)的操作是重要的。因此,在较高温度下具有高质子电解膜的无水电解质膜的发展存在大量研究[1-4]。一种方法是使用含氮的芳族杂环分子 - 沸点高于水 - 作为质子载体的沸点,作为掺杂剂或固定在聚合物主链中,源自固有质子电导率的聚合物。 1H-1,2,3-苯并三唑(BTRI)是一种新型杂环分子,分别熔融和沸点为100和350℃。以前,将其用作聚乙烯膦酸中的掺杂剂,并报告了Nation和高质子电导率(150℃的10〜3 s / cm)[5]。在该研究中,我们通过将磺化聚(乙烯醇)(PVA)与高质子交换能力和有机碱杂环,1 H-1,2,3-苯并三唑混合制备酸碱复合材料。通过用磺酸(SSA)通过酯化通过磺酸(SSA)来改变PVA的化学结构,在各种摩尔比以各种摩尔比引入PVA基质中。将得到的交联聚合物以几摩尔比(表1)与1h-1,2,3-苯并三唑共混物(表1),得到将酸基团固定在链中的酸基团和与基质中的酸基团相互作用的酰胺。该聚合物的特征在于傅里叶变换红外(FT-IR),热重分析(TGA)和差示扫描量热法(DSC)。通过阻抗光谱仪研究无水样品的质子电导率,并将结果与​​先前报道的系统进行比较。

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