کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6610829 | 459557 | 2015 | 32 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Efficient conversion of waste polyvinyl chloride into nanoporous carbon incorporated with MnOx exhibiting superior electrochemical performance for supercapacitor application
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی شیمی
مهندسی شیمی (عمومی)
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چکیده انگلیسی
We herein demonstrate a rational template carbonization approach to convert waste polyvinyl chloride into nanoporous carbon, in which inexpensive Mg(OH)2 serves as hard template. The carbon-blank sample that is obtained by designating the mass ratio of polyvinyl chloride and Mg(OH)2 as 1:2 at the carbonization temperature of 700 °C is amorphous and highly porous in essence. It also exhibits large BET surface area of 958.6 m2 gâ1, high pore volume of 3.56 cm3 gâ1, and hierarchical pore size distribution. To further improve the electrochemical performance, various amounts of MnOx nanoparticles are incorporated into the nanoporous carbon by direct redox reaction between carbon-blank sample and KMnO4 solution at 70 °C. Therein, carbon-Mn2 sample (the mass ratio of carbon-blank sample and KMnO4 is 1:1) behaves the optimal electrochemical performance. Though its porosity to some extent decreases, its specific capacitance has greatly elevated up to 751.5 F gâ1 at 1.0 A gâ1, compared with that of the carbon-blank sample (â¼47.8 F gâ1). The incremental capacitance of the carbon-Mn2 sample is mostly attributed to the contribution of pseudocapacitance incurred by faradic reaction of MnOx material. The present synthesis method opens up an avenue to properly dispose waste polyvinyl chloride into nanoporous carbon, especially with the promise in supercapacitor application.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Electrochimica Acta - Volume 176, 10 September 2015, Pages 197-206
Journal: Electrochimica Acta - Volume 176, 10 September 2015, Pages 197-206
نویسندگان
Liang Xiao Cheng, Lei Zhang, Xiang Ying Chen, Zhong Jie Zhang,