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主管单位 中华人民共和国
工业和信息化部
主办单位 哈尔滨工业大学 主编 李隆球 国际刊号ISSN 0367-6234 国内刊号CN 23-1235/T

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引用本文:赵纯,丁昊杰,程诺,刘臻,张键,郑怀礼,邓慧萍.阴极电场活化过硫酸盐原位再生饱和活性炭纤维[J].哈尔滨工业大学学报,2021,53(5):9.DOI:10.11918/201907220
ZHAO Chun,DING Haojie,CHENG Nuo,LIU Zhen,ZHANG Jian,ZHENG Huaili,DENG Huiping.In situ regeneration of saturated activated carbon fibers by cathodic electric field activated persulfate process[J].Journal of Harbin Institute of Technology,2021,53(5):9.DOI:10.11918/201907220
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阴极电场活化过硫酸盐原位再生饱和活性炭纤维
赵纯1,2,丁昊杰2,程诺2,刘臻2,张键2,3,郑怀礼2,邓慧萍4
(1.煤矿灾害动力学与控制国家重点实验室(重庆大学),重庆 400044; 2.三峡库区生态环境教育部重点实验室(重庆大学),重庆 400045; 3.石河子大学 水利建筑工程学院,新疆 石河子 832003; 4.同济大学 环境科学与工程学院,上海 200092)
摘要:
针对传统电再生活性炭过程中存在的高能耗、再生液二次污染严重等问题,采用阴极电场活化过硫酸盐原位再生苯酚饱和活性炭纤维(ACF),考察ACF的再生效能以及再生液中污染物的降解效能.通过Langmuir和Freundlich吸附等温模型对ACF吸附的过程进行拟合;探究电流密度、过硫酸盐浓度、再生时间对电阴极/过硫酸盐再生体系的影响;通过ACF的多次吸附饱和-再生循环实验分析该体系应用潜力并阐述再生机理.结果表明:ACF对苯酚的吸附更符合Freundlich吸附等温模型,为非均一吸附;电阴极/过硫酸盐体系的再生效率为62.71%,且再生液中苯酚总量仅为ACF最大吸附容量的3.10%;最优工况为电流密度57.14 mA/cm2,过硫酸盐浓度0.1 mol/L,再生时间6 h.在电阴极/过硫酸盐体系多次再生的过程中,过硫酸盐及其产生的硫酸根自由基会对ACF的孔隙结构和表面形貌产生一定的破坏.3次再生后,再生效率仍能达到40%左右,表明该体系具有较强的应用潜力.
关键词:  电化学再生  活性炭纤维  过硫酸盐  硫酸根自由基  苯酚
DOI:10.11918/201907220
分类号:X703.1
文献标识码:A
基金项目:国家自然科学基金(51308563);大型仪器基金(201406150031);中央高校基本科研业务费专项课题(2019CDXYCH0027)
In situ regeneration of saturated activated carbon fibers by cathodic electric field activated persulfate process
ZHAO Chun1,2,DING Haojie2,CHENG Nuo2,LIU Zhen2,ZHANG Jian2,3,ZHENG Huaili2,DENG Huiping4
(1.State Key Laboratory of Coal Mine Disaster Dynamics and Control (Chongqing University), Chongqing 400044, China; 2.Key Laboratory of the Three Gorges Reservoir Region’s Environment (Chongqing University), Ministry of Education, Chongqing 400045, China; 3. College of Water & Architectural Engineering, Shihezi University, Shihezi 832003, Xinjiang, China; 4.College of Environmental Science and Engineering, Tongji University, Shanghai 200092, China)
Abstract:
In view of the problems of high energy consumption and serious secondary pollution during traditional electric regeneration of activated carbon, cathodic electric field was adopted to activate persulfate in situ for regenerating phenol saturated activated carbon fiber (ACF), and the regeneration efficiency of ACF and degradation efficiency of pollutants in the regeneration solution were investigated. The adsorption process of ACF was fitted by Langmuir and Freundlich adsorption isotherm models. The effects of current density, persulfate concentration, and regeneration time on the electric cathode/persulfate regeneration process were investigated. Besides, the application potential and regeneration mechanism were analyzed by multiple adsorption–regeneration cycles experiments. Results show that the adsorption of phenol by ACF was more consistent with the Freundlich adsorption isotherm model, indicating heterogeneous adsorption. The regeneration efficiency of the electric cathode/persulfate regeneration process was 62.71%, and the total amount of phenol in the regeneration solution was only 3.10% of the maximum adsorption capacity of ACF. The optimal operating conditions were current density of 57.14 mA/cm2, persulfate concentration of 0.1 mol/L, and regeneration time of 6 h. During the multiple regeneration of the electric cathode/persulfate process, the persulfate and the resulting sulfate radical would damage the pore structure and surface morphology of ACF to some extent. After three times of regeneration, the regeneration efficiency could still reach about 40%, which indicates that the process has strong application potential.
Key words:  electrochemical regeneration  activated carbon fiber (ACF)  persulfate  sulfate radical  phenol

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