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In-situ catalytic co-pyrolysis of yellow poplar and high-density polyethylene over mesoporous catalysts

机译:黄杨与高密度聚乙烯在介孔催化剂上的原位催化共热解

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摘要

Catalytic co-pyrolysis of biomass and hydrogen-rich materials is an effective approach for enhancing the production of bio-based hydrocarbons. In this work, mesoporous solid acid materials, such as hierarchical mesoporous MFI (meso MFI), hierarchical mesoporous Y (meso Y) and Al-SBA-15, were used as the catalysts for the catalytic co-pyrolysis of yellow poplar (YP) and high-density polyethylene (HDPE). Among three catalysts, meso MFI revealed the highest catalytic efficiency for the production of aromatic hydrocarbons from catalytic pyrolysis of YP or HDPE due to its effective pore structure, large channels, and high acidity. Moreover, meso MFI showed the highest synergistic formation of aromatic hydrocarbons during the catalytic co-pyrolysis of YP and HDPE as a result of hydrogen donating effect of HDPE and catalytic interactions between YP- and HDPE-derived pyrolyzates. The amounts of solid residue obtained from the catalytic co-pyrolysis of YP and HDPE over meso MFI were also much lower than their theoretical yields.
机译:生物质和富氢材料的催化共热解是提高生物基碳氢化合物产量的有效方法。在这项工作中,介孔固体酸材料,例如分级介孔MFI(介孔MFI),分级介孔Y(介孔Y)和Al-SBA-15,被用作黄杨(YP)催化共热解的催化剂和高密度聚乙烯(HDPE)。在三种催化剂中,中观MFI由于其有效的孔结构,大通道和高酸度,显示出YP或HDPE催化热解生产芳烃的最高催化效率。此外,由于HDPE的氢给氢作用以及YP和HDPE衍生的热解产物之间的催化相互作用,在YP和HDPE的催化共热解过程中,中观MFI显示出最高的协同形成芳烃的能力。 YP和HDPE在介孔MFI上催化共热解得到的固体残留物的量也远低于其理论收率。

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