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Hydrogen Production from Glycerol and Plastics by Sorption-Enhanced Steam Reforming

热解 化学工程 氧化钙 材料科学 甘油 制氢 焦炭 催化作用 吸附 产量(工程) 蒸汽重整 聚乙烯 吸附 废物管理 化学 有机化学 冶金 复合材料 工程类
作者
Petch Chunakiat,Nipitpon Panarmasar,Prapan Kuchonthara
出处
期刊:Industrial & Engineering Chemistry Research [American Chemical Society]
卷期号:62 (49): 21057-21066
标识
DOI:10.1021/acs.iecr.3c02072
摘要

Hydrogen (H2) serves as a vital precursor in numerous processes, and it is envisioned to serve as a clean energy source in the future. The utilization of waste materials for the production of H2 presents a noteworthy opportunity to advance the sustainability of H2-based energy. In this study, the effect of cofeeding three different types of plastic, polyethylene (PE), polypropylene (PP), and polystyrene (PS), with glycerol was investigated in the two-step process of pyrolysis and steam reforming (PSR) to produce H2. Experiments were performed using a two-stage fixed bed reactor at 973 K. For each type of plastic, the yield of H2 in the copresence of glycerol was higher than the combined yield of that from the plastic and glycerol separately. This result demonstrated the effectiveness of the synergistic relationship between plastics and glycerol in enhancing H2 production through PSR. Among the plastics, PE gave the highest H2 yield followed by PP and PS. Bifunctional nickel oxide/calcium oxide (NiO-CaO) catalysts were synthesized for the pyrolysis sorption-enhanced steam reforming process (PSESR) of plastics with glycerol at 973 K. The maximum H2 yield was obtained from the PSESR of PE with glycerol when using a NiCa/silica fiber (SF) catalyst. Using NiO combined with CaO in PSESR can promote the cracking of volatile pyrolysis products, reducing the coke deposition and increasing CO2 adsorption. Furthermore, the nonporous structure of the SF support afforded easier access to the active sites in comparison to the conventional porous alumina support.

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