کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8961309 | 1646478 | 2018 | 10 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
HT-PEMs based on nitrogen-heterocycle decorated poly (arylene ether ketone) with enhanced proton conductivity and excellent stability
دانلود مقاله + سفارش ترجمه
دانلود مقاله ISI انگلیسی
رایگان برای ایرانیان
کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
شیمی
الکتروشیمی
پیش نمایش صفحه اول مقاله

چکیده انگلیسی
The proton transport can be enhanced by properly controlling the chemical structure of side chains. In this work, polyelectrolytes supported on poly (arylene ether ketone), decorated with four kinds of nitrogen-heterocycles, were prepared as alternative materials for high-temperature proton exchange membrane (HT-PEM) applications. Particularly, the “prominent basic” alongside backbone makes positive imidazole group more effective than other three to promote phosphoric acid doping, enhance proton conductivity and avoid phosphoric acid leakage. The obtained BrPAEK-MeIm1.6 membranes (1.6 imidazole/unit), with PA doping level of 19.2 in 1 h acid absorption process, exhibited the conductivity of 0.091 S cmâ1 at 170 °C. Under harsh experimental conditions, membrane with higher imidazole exhibited relatively higher phosphoric acid retention ability (27% enhancement). The stability of proton conductivity has also been demonstrated, which indicates that the PA/BrPAEK-MeIm1.6 come to an equilibrium state with 77.7% of initial conductivity after 5 h. Then, there is almost negligible conductivity loss within 30 h. These results provide a basic understanding of nitrogen-heterocyclic addition and PA absorption and open up avenues for further research in this area.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: International Journal of Hydrogen Energy - Volume 43, Issue 33, 16 August 2018, Pages 16248-16257
Journal: International Journal of Hydrogen Energy - Volume 43, Issue 33, 16 August 2018, Pages 16248-16257
نویسندگان
Jinsheng Li, Shuang Wang, Fengxiang Liu, Xue Tian, Xu Wang, Hao Chen, Tiejun Mao, Zhe Wang,