Pyrolysis of lignocellulosic biomass with high-density polyethylene to produce chemicals and bio-oil with high liquid yields

热解 高密度聚乙烯 生物量(生态学) 烧焦 材料科学 木质纤维素生物量 聚乙烯 化学工程 燃烧热 催化作用 热解油 有机化学 柴油 制浆造纸工业 化学 木质素 燃烧 农学 工程类 生物
作者
Witchakorn Charusiri,Naphat Phowan,Tharapong Vitidsant
出处
期刊:Sustainable Chemistry and Pharmacy [Elsevier BV]
卷期号:25: 100567-100567 被引量:22
标识
DOI:10.1016/j.scp.2021.100567
摘要

The pyrolysis of waste plastic and lignocellulosic material feedstocks increases the hydrogen/carbon ratio of the plastic-biomass mixture and may be advantageous for refining the properties of pyrolysis oil, which can be directly used as a fuel without any need for upgrading by catalytic hydrodeoxygenation. In this paper, high-density polyethylene (HDPE) and brown salwood were tested in a custom-built laboratory-scale fixed-bed reactor to investigate the co-pyrolysis reaction at temperatures ranging from 500 to 650 °C, nitrogen flow rates ranging from 40 to 160 mL min−1, and HDPE-to-biomass ratios ranging from 0.1 to 0.9. The results revealed that the temperature mostly influenced the pyrolysis products, whereas increasing the temperature to 600 °C promoted pyrolysis oil production, reaching a yield of 35.10 ± 1.20 wt%. Further increasing the reaction temperature to 650 °C decreased the yield to 34.57 ± 0.49 wt% because secondary cracking reactions produce a noncondensable gas rich in hydrocarbons. Physicochemical analysis of the pyrolyzed organic phase revealed a gross calorific heating value of up to approximately 38.19 MJ kg−1. Additionally, co-pyrolysis of HDPE improved the production of furans, and acid derivatives were obtained in the aqueous fraction via the thermal conversion of hemicellulose and lignin; conversely, the obtained char exhibited a notably low surface area and few superficial micropores and was used to further develop activated carbon for use as a catalyst in the catalytic pyrolysis of waste materials.
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