Employing CO2 as reaction medium for in-situ suppression of the formation of benzene derivatives and polycyclic aromatic hydrocarbons during pyrolysis of simulated municipal solid waste

被引:37
作者
Lee, Jechan [1 ]
Choi, Dongho [1 ]
Tsang, Yiu Fai [2 ]
Oh, Jeong-Lk [3 ]
Kwon, Eilhann E. [1 ]
机构
[1] Sejong Univ, Dept Environm & Energy, Seoul 05006, South Korea
[2] Educ Univ Hong Kong, Dept Sci & Environm Studies, Tai Po, Hong Kong, Peoples R China
[3] Land & Housing Inst, Adv Technol Dept, Daejeon 34047, South Korea
基金
新加坡国家研究基金会;
关键词
Biomass; Polymer; Carbon dioxide; Municipal solid waste; Waste disposal; Waste-to-energy; THERMAL-DEGRADATION; COAL-GASIFICATION; CARBON-DIOXIDE; MSW; BIOMASS; MECHANISMS; WOOD; PAH; TEMPERATURE; EMISSIONS;
D O I
10.1016/j.envpol.2017.02.028
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This study proposes a strategic principle to enhance the thermal efficiency of pyrolysis of municipal solid waste (MSW). An environmentally sound energy recovery platform was established by suppressing the formation of harmful organic compounds evolved from pyrolysis of MSW. Using CO2 as reaction medium/feedstock, CO generation was enhanced through the following: 1) expediting the thermal cracking of volatile organic carbons (VOCs) evolved from the thermal degradation of the MSWs and 2) directly reacting VOCs with CO2. This particular influence of CO2 on pyrolysis of the MSWs also led to the in-situ mitigation of harmful organic compounds (e.g., benzene derivatives and polycyclic aromatic hydrocarbons (PAHs)) considering that CO2 acted as a carbon scavenger to block reaction pathways toward benzenes and PAHs in pyrolysis. To understand the fundamental influence of CO2, simulated MSWs (i.e., various ratios of biomass to polymer) were used to avoid any complexities arising from the heterogeneous matrix of MSW. All experimental findings in this study suggested the foreseeable environmental application of CO2 to energy recovery from MSW together with disposal of MSW. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:476 / 483
页数:8
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