Preparation and electrochemical performance of activated carbon microspheres from recycled novolak phenol formaldehyde

被引:11
作者
Guan, Mingjie [1 ,2 ]
Li, Hui [1 ]
Chen, Xianwen [1 ]
Zhang, Shu [1 ]
机构
[1] Nanjing Forestry Univ, Coll Mat Sci & Engn, Nanjing 210037, Peoples R China
[2] Nanjing Forestry Univ, Coinnovat Ctr Efficient Proc & Utilizat Forest Re, Nanjing 210027, Peoples R China
基金
中国国家自然科学基金;
关键词
Porous activated carbon microspheres; Recycled novolak phenol formaldehyde; Hydrothermal method; Supercapacitors; PRINTED-CIRCUIT BOARD; POROUS CARBON; WASTE-WATER; TEMPLATE SYNTHESIS; RESIN; ADSORPTION; COMPOSITES; ELECTRODES; SEPARATION; PROGRESS;
D O I
10.1016/j.wasman.2020.10.022
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this study, an attempt is made to obtain porous activated carbon microspheres (ACMs) as supercapacitor electrodes by recycling waste novolak phenol formaldehyde (NPF) resins. These NPF-ACMs were prepared by a three-step procedure of hydrothermal synthesis, carbonization, and activation in turn. The effects of temperature, time, and sodium dodecyl sulfonate (SDS) addition on NPF-based microspheres were studied by the orthogonal method. The optimal preparation process of NPF-based microspheres was the following: 230 degrees C, 4 h, and a mass ratio of SDS: NPF of 24:1 by hydrothermal synthesis. Based on the above optimal conditions, NPF-ACMs were made, the yield of the microspheres after carbonization and chemical activation are 54% and 38%, and their electrochemical properties were analyzed. The NPF-ACMs had uniform size, a high surface area of 2528 m(2) g(-1), good dispersion, a low impedance of 0.46 Omega, highest specific capacitance of 118.6 F g(-1) at 0.5 A g(-1), good rate capability with 79% retention from 0.1 to 10 A g(-1). Moreover, it showed high capacitance retention of 99.5% after 1000 cycles at a scan rate of 5 mV s(-1). The results showed that waste NPF can be used as promising ACMs of the electrode material to increase its utilization value. (C)) 2020 Elsevier Ltd. All rights reserved.
引用
收藏
页码:635 / 641
页数:7
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