污泥生物炭负载Ni-M双金属催化剂原位催化分解城市生活垃圾气化排放氨

Xueyu Ding, Yaji Huang, Xinxin Dong, Jiaqi Zhao, Mengzhu Yu, Xinqi Tian, Jinlei Li, Xuewei Zhang, Yuxin Li, Zekun Wei
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引用次数: 1

摘要

气化技术可以有效地实现城市生活垃圾的能源回收,减少其对环境的负面影响。然而,氨作为城市生活垃圾气化产生的污染物,其排放被认为对人类有害,需要进行处理。本工作旨在通过原位催化法分解城市生活垃圾气化产生的NH3污染物。生活垃圾样品由大米、纸张、聚苯乙烯颗粒、橡胶手套、纺织品和木屑组成。采用共浸渍法制备了Ni-M (M=Co, Fe, Zn)双金属催化剂,并用x射线衍射、N2等温吸附、扫描电镜、透射电镜和NH3程序升温脱附等手段对催化剂进行了表征。在实验之前,先将催化剂与生活垃圾样品均匀混合,然后在卧式固定床反应器中进行原位催化试验。比较了第二金属(Co, Fe, Zn)对催化性能的影响,筛选了最佳的Ni-M双金属。结果表明,Ni-Co /SSC催化剂对NH3的分解活性最好,在650℃时,NH3的分解率达到40.21%。Ni - Co/SSC的最佳催化性能可以解释为其较小的Ni粒径有利于活性位点的分散,以及Co的加入降低了NH3分解过程中NH物质缔合分解的能垒。在450℃~ 700℃范围内,Ni-Co /SSC的活性增加,因为NH3分解反应为吸热反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In-situ catalytic decomposition of emitted ammonia from municipal solid waste gasification by Ni–M bimetallic catalysts supported on sewage sludge-derived biochar

In-situ catalytic decomposition of emitted ammonia from municipal solid waste gasification by Ni–M bimetallic catalysts supported on sewage sludge-derived biochar

Gasification technology can effectively realize energy recovery from municipal solid waste (MSW) to reduce its negative impact on the environment. However, ammonia, as a pollutant derived from MSW gasification, needs to be treated because its emission is considered harmful to mankind. This work aims to decompose the NH3 pollutant from MSW gasification by an in-situ catalytic method. The MSW sample is composed of rice, paper, polystyrene granules, rubber gloves, textile and wood chips. Ni–M (M=Co, Fe, Zn) bimetallic catalysts supported on sewage sludge-derived biochar (SSC) were prepared by co-impregnation method and further characterized by X-ray diffraction, N2 isothermal adsorption, scanning electron microscopy, transmission electron microscopy and NH3 temperature programmed desorption. Prior to the experiments, the catalysts were first homogeneously mixed with the MSW sample, and then in-situ catalytic tests were conducted in a horizontal fixed-bed reactor. The effect of the second metal (Co, Fe, Zn) on the catalytic performance was compared to screen the best Ni-M dual. It was found that the Ni–Co/SSC catalyst had the best activity toward NH3 decomposition, whose decomposition rate reached 40.21% at 650 °C. The best catalytic performance of Ni–Co/SSC can be explained by its smaller Ni particle size that facilitates the dispersion of active sites as well as the addition of Co reducing the energy barrier for the associative decomposition of NH species during the NH3 decomposition process. Besides, the activity of Ni–Co/SSC increased from 450 °C to 700 °C as the NH3 decomposition reaction was endothermic.

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