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Recycling benzene and ethylbenzene from in-situ catalytic fast pyrolysis of plastic wastes  ( SCI-EXPANDED收录)   被引量:43

文献类型:期刊文献

英文题名:Recycling benzene and ethylbenzene from in-situ catalytic fast pyrolysis of plastic wastes

作者:Wang, Jia[1,2,3,4,5] Jiang, Jianchun[1,2,3] Sun, Yunjuan[2,3] Zhong, Zhaoping[4] Wang, Xiaobo[6] Xia, Haihong[2,3] Liu, Guanghua[7] Pang, Shusheng[8] Wang, Kui[2,3] Li, Mi[5] Xu, Junming[2,3] Ruan, Roger[9,10] Ragauskas, Arthur J.[5,11,12]

第一作者:Wang, Jia;王婧

通信作者:Jiang, JC[1]

机构:[1]Nanjing Forestry Univ, Coll Chem Engn, Longpan Rd 159, Nanjing 210037, Jiangsu, Peoples R China;[2]Chinese Acad Forestry, Inst Chem Ind Forest Prod, 16 Suojin Five Village, Nanjing 210042, Jiangsu, Peoples R China;[3]Nanjing Forestry Univ, Coinnovat Ctr Efficient Proc & Utilizat Forest Re, Longpan Rd 159, Nanjing 210037, Jiangsu, Peoples R China;[4]Southeast Univ, Minist Educ, Key Lab Energy Thermal Convers & Control, 2 Sipailou, Nanjing 210096, Jiangsu, Peoples R China;[5]Univ Tennessee, Dept Chem & Biomol Engn, Knoxville, TN 37996 USA;[6]Nanjing Xiaozhuang Univ, Sch Environm Sci, Nanjing 211171, Jiangsu, Peoples R China;[7]Dongguan Baida New Energy Co Ltd, Dongguan 523001, Guangdong, Peoples R China;[8]Univ Canterbury, Dept Chem & Proc Engn, Christchurch, New Zealand;[9]Univ Minnesota, Ctr Biorefining, 1390 Eckles Ave, St Paul, MN 55108 USA;[10]Univ Minnesota, Dept Bioprod & Biosyst Engn, 1390 Eckles Ave, St Paul, MN 55108 USA;[11]Univ Tennessee, Inst Agr, Ctr Renewable Carbon, Dept Forestry Wildlife & Fisheries, Knoxville, TN 37996 USA;[12]Oak Ridge Natl Lab, Biosci Div, Joint Inst Biol Sci, Oak Ridge, TN 37831 USA

年份:2019

卷号:200

外文期刊名:ENERGY CONVERSION AND MANAGEMENT

收录:;WOS:【SCI-EXPANDED(收录号:WOS:000495520600034)】;

基金:The authors are grateful for the National Natural Science Foundation of China (No. 31530010), the Guangdong Innovative and Entrepreneurial Research Team Program (No. 2016ZT06N467), the National Natural Science Foundation of China (No. 31870714), the Key Lab. of Biomass Energy and Material, Jiangsu Province (No. JSBEM-S-201602), the Talent Introduction Project Funded by National Forestry and Grassland Administration (No. KJZXSF2019002), and the Natural Science Foundation of the Jiangsu Higher Education Institutions of China (No. 17KJB610005).

语种:英文

外文关键词:Polystyrene; Thermochemical conversion; Aromatic hydrocarbons; USY zeolites

摘要:Recovering waste plastics by catalytic fast pyrolysis to selectively generate aromatic hydrocarbons is a promising approach to dispose of solid wastes. In the present work, catalytic conversion of polystyrene over ultra-stable Y zeolites (USY) was conducted to directionally produce benzene and ethylbenzene. Experimental results indicated that catalyst type considerably affected the distribution of aromatic hydrocarbons, and USY with high surface area (734 m(2)/g), large pore size (5.6 nm), and an abundant amount of strong acid sites (1.21 mmol/g) exhibited the most effective shape selectivity for ethylbenzene and benzene generation as the yield enhanced rate reached 401.8% and 61.1%, respectively. Plastic type also played a vital role in the formation of desirable aromatic hydrocarbons, and polystyrene was more beneficial to the production of ethylbenzene as a 54-fold increase was obtained compared to polycarbonate in the catalytic degradation process. Concerning reaction conditions to maximize the formation of benzene and ethylbenzene in the catalytic decomposition of polystyrene, the catalyst/feedstock mass ratio, Si/Al mole ratio in USY, and catalytic conversion temperature could be optimized at 1.5, 5.3, and 650 degrees C, respectively.

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