Catalytic Pyrolysis of Polypropylene to Benzene, Toluene, and Xylene (BTX) Using a Double-Fluidized-Bed Reactor

被引:0
|
作者
Wang, Hongqi [1 ]
van Akker, Matthijs [2 ]
Winkelman, Jozef G. M. [1 ]
Heeres, Andre [3 ]
Heeres, Hero Jan [1 ]
机构
[1] Univ Groningen, Engn & Technol Inst, Green Chem React Engn, NL-9747 AG Groningen, Netherlands
[2] BioBTX BV, NL-9747 AA Groningen, Netherlands
[3] Hanze Univ Appl Sci, NL-9747 AS Groningen, Netherlands
关键词
HIGH-DENSITY POLYETHYLENE; CRACKING CATALYSTS; PLASTIC WASTE; AROMATICS; DEGRADATION; BIOMASS; FUELS;
D O I
10.1021/acs.energyfuels.4c05316
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The current plastic value chain is highly linear, leading to large amounts of waste plastics that harm the environment and human health. Recycling is required, and among the options, catalytic pyrolysis is particularly suited to convert polyolefin-rich plastic waste into useful chemicals such as benzene, toluene, and xylene (BTX). In this paper, we demonstrate ex situ catalytic pyrolysis of polypropylene in a continuous double-fluidized-bed reactor to produce BTX. The optimal pyrolysis temperature in the first fluidized-bed reactor was 550 degrees C, giving a BTX yield of 22.3 wt % (based on PP input). Lowering the nitrogen flow rate and the use of smaller catalyst particle sizes favor BTX formation. Our novel reactor concept showed good operational stability at longer times on stream (TOS, 10 h). Catalyst activity was slightly reduced during TOS, as is evident from a small decrease in BTX yields. Detailed catalyst characterization studies showed that coke formation is the main reason for catalyst deactivation. In addition, chemoselectivity was also a function of TOS and the selectivity to benzene and toluene decreased, while higher amounts of xylenes were formed.
引用
收藏
页码:3564 / 3574
页数:11
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