生物炭
催化作用
碳热反应
热解
二甲苯
低密度聚乙烯
化学
聚乙烯
催化裂化
木质素
聚丙烯
材料科学
有机化学
化学工程
甲苯
核化学
工程类
相(物质)
作者
Pei Huang,Wenguang Zhou,Kuangli Jin,Yunpu Wang,Jun Qian,Lei Liu,Hongyu Peng,Jiabo Wu,Jinye Hu,Mengjiao Wang,Weixin Wang,Ting Luo,Liangliang Fan
标识
DOI:10.1021/acssuschemeng.2c05804
摘要
A novel biochar-supported metal catalyst was prepared in this study using a one-step carbothermal reduction synthesis method for the catalytic pyrolysis of plastics. Several catalysts with different metals (Cu, Fe, Ni, and Ru) loaded on three biochar supports from lignin, soybean straw, and Chlorella vulgaris were evaluated using XRD, FTIR, NH3-TPR, and TEM. Zerovalent metal nanoparticles, including Ni, Cu, and Ru, and various functional groups were observed on the biochar surface. The chemical selectivities of gasoline hydrocarbons (C4–C12 hydrocarbons) reached 76.2% with a remarkable catalytic cracking effect of Ni/lignin biochar on low density polyethylene (LDPE). Catalytic performance was comparable to that of the Ru-based catalyst, which contributed to 85.6% of gasoline hydrocarbons. The Ni/lignin catalytic cracking of plastic waste simulated by LDPE, polypropylene (PP), and polystyrene (PS) showed a maximum selectivity of 87.9% for C4–C12 hydrocarbons and yields of 78.1 mg/g for benzene, toluene, and xylene (BTX). The mechanism related to the cleavage of long chain radicals of polyethylene, polypropylene, and polystyrene as well as the aromatization of aliphatics were proposed.
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