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用于城市固体废物增值利用的基于赤泥的多孔纳米催化剂。

Red-mud based porous nanocatalysts for valorisation of municipal solid waste.

作者信息

Ahmed Mohamed H M, Batalha Nuno, Qiu Tengfei, Hasan Md Mahmudul, Atanda Luqman, Amiralian Nasim, Wang Lianzhou, Peng Hong, Konarova Muxina

机构信息

Nanomaterials Centre, Australian Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, Brisbane 4072, Australia.

School of Chemical Engineering, The University of Queensland, Brisbane 4072, Australia.

出版信息

J Hazard Mater. 2020 Sep 5;396:122711. doi: 10.1016/j.jhazmat.2020.122711. Epub 2020 Apr 23.

Abstract

Red mud samples were used to catalyse in-situ co-pyrolysis of pinewood and low-density polyethylene for the production of high-quality bio-oil. The sodium cation in the crude red-mud was exchanged with barium and calcium cations and further tested to explore their role in oil upgrading. The relationship between red-mud catalytic activity and its constituents was explored using synthetic sodalite. The red-mud catalysts exhibited a considerable aromatisation capacity compared to the thermal co-pyrolysis, as the selectivity towards monocyclic aromatic hydrocarbons increased from 12.7 to 19.6%, respectively. Long-chain molecules cracking was more significant in synthetic sodalite associated with their acidic active sites. The addition of barium and calcium cations to the red-mud largely improved oxygen elimination as a result of the enhanced catalyst basicity. In contrast, the aromatisation ability of red-mud significantly impeded by the large cation size (Ba and Ca) due to the limited diffusion of pyrolysis vapours to the active sites. Ba-exchanged red-mud catalysts reduced the content of carboxylic acids in the bio-oil to 1.8 % while maintained a high yield of the organic fraction (34 %). Ca-exchanged red-mud catalysts produced the lowest fraction of oxygenated compounds (35.1 %); however, the organic phase yield was as low as 23.6 %. The modified red-mud catalysts reduced the fraction of oxygenated compounds from 69.9-35.1% during the biomass-plastic co-pyrolysis.

摘要

采用赤泥样品催化松木和低密度聚乙烯的原位共热解,以生产高质量生物油。将粗赤泥中的钠离子与钡离子和钙离子进行交换,并进一步测试以探索它们在油品提质中的作用。使用合成方钠石探索了赤泥催化活性与其成分之间的关系。与热共热解相比,赤泥催化剂表现出相当可观的芳构化能力,因为对单环芳烃的选择性分别从12.7%提高到了19.6%。在与酸性活性位点相关的合成方钠石中,长链分子的裂解更为显著。由于催化剂碱性增强,向赤泥中添加钡离子和钙离子大大改善了氧的脱除。相比之下,由于热解蒸汽向活性位点的扩散受限,大阳离子尺寸(钡和钙)显著阻碍了赤泥的芳构化能力。钡交换赤泥催化剂将生物油中羧酸的含量降低到1.8%,同时保持了较高的有机馏分产率(34%)。钙交换赤泥催化剂产生的含氧化合物馏分最低(35.1%);然而,有机相产率低至23.6%。改性赤泥催化剂在生物质-塑料共热解过程中将含氧化合物的馏分从69.9%降低到了35.1%。

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