CO2-mediated pyrolysis for syngas generation from wood-plastic composite waste

被引:0
作者
Kwon, Dohee [1 ]
Kim, Jee Young [1 ]
Song, Hocheol [1 ]
Lee, Jaewon [2 ]
Tsang, Yiu Fai [3 ,4 ]
Kwon, Eilhann E. [1 ]
机构
[1] Hanyang Univ, Dept Earth Resources & Environm Engn, Seoul 04763, South Korea
[2] Hanyang Univ, Dept Mat Sci & Chem Engn, Ansan 15588, South Korea
[3] Educ Univ Hong Kong, Dept Sci & Environm Studies, Tai Po, Hong Kong 999077, Peoples R China
[4] Educ Univ Hong Kong, State Key Lab Marine Pollut, Tai Po, Hong Kong 999077, Peoples R China
基金
新加坡国家研究基金会;
关键词
Wood plastic composite; Waste-to-Energy; Pyrolysis; Syngas; Carbon dioxide; MINERAL FILLERS; CO2; BIOMASS; DOLOMITE; DECOMPOSITION; TEMPERATURE; CONVERSION; KINETICS;
D O I
10.1016/j.energy.2025.134917
中图分类号
O414.1 [热力学];
学科分类号
摘要
Wood-plastic composites (WPCs) are extensively utilized in construction, furniture, and outdoor applications due to their superior physicochemical properties. However, their low biodegradability presents a critical challenge for waste management. This study explores upcycling WPC waste into syngas via CO2-mediated pyrolysis. CO2 serves as reaction medium, enhancing thermal decomposition and partial oxidation of volatile matters (VMs) generated from pyrolysis of WPCs to form carbon monoxide (CO) through homogeneous reactions. To further optimize the role of CO2, a multi-stage pyrolysis operating isothermally at 700 degrees C was employed. In this configuration, the reactivity of CO2 was more pronounced at lower temperatures than that during single-stage pyrolysis, indicating that the additional thermal energy accelerated CO2-induced reactions. The introduction of a nickel-based catalyst accelerated the CO2-induced homogeneous reactions by facilitating the adsorption and reaction of CO2 with VMs during pyrolysis. Thus, utilizing CO2 as a reaction medium in the catalytic pyrolysis process represents a strategic pathway for the upcycling of WPC waste.
引用
收藏
页数:11
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