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负载于还原氧化石墨烯上的铈和锡氧化物用于低温下NH₃选择性催化还原NO

Cerium and tin oxides anchored onto reduced graphene oxide for selective catalytic reduction of NO with NH at low temperatures.

作者信息

Wang Yanli, Kang Ying, Ge Meng, Zhan Liang

机构信息

State Key Laboratory of Chemical Engineering, Key Laboratory for Specially Functional Polymers and Related Technology of Ministry of Education, Shanghai Key Laboratory of Multiphase Materials Chemical Engineering, East China University of Science and Technology Shanghai 200237 China

CAS Key Laboratory of Carbon Materials, Institute of Coal Chemistry, Chinese Academy of Sciences Taiyuan 030001 China.

出版信息

RSC Adv. 2018 Oct 26;8(63):36383-36391. doi: 10.1039/c8ra05151h. eCollection 2018 Oct 22.

Abstract

A series of cerium and tin oxides anchored on reduced graphene oxide (CeO-SnO /rGO) catalysts are synthesized using a hydrothermal method and their catalytic activities are investigated by selective catalytic reduction (SCR) of NO with NH in the temperature range of 120-280 °C. The results indicate that the CeO-SnO /rGO catalyst shows high SCR activity and high selectivity to N in the temperature range of 120-280 °C. The catalyst with a mass ratio of (Ce + Sn)/GO = 3.9 exhibits NO conversion of about 86% at 160 °C, above 97% NO conversion at temperatures of 200-280 °C and higher than 95% N selectivity at 120-280 °C. In addition, the catalyst presents a certain SO resistance. It is found that the highly dispersed CeO nanoparticles are deposited on the surface of rGO nanosheets, because of the incorporation of Sn into the lattice of CeO. The mesoporous structures of the CeO-SnO /rGO catalyst provides a large specific surface area and more active sites for facilitating the adsorption of reactant species, leading to high SCR activity. More importantly, the synergistic interaction between cerium and tin oxides is responsible for the excellent SCR activity, which results in a higher ratio of Ce/(Ce + Ce), higher concentrations of surface chemisorbed oxygen and oxygen vacancies, more strong acid sites and stronger acid strength on the surface of the CeSn(3.9)/rGO catalyst.

摘要

采用水热法合成了一系列负载在还原氧化石墨烯(CeO-SnO /rGO)上的铈和锡氧化物催化剂,并在120-280℃温度范围内通过NH对NO的选择性催化还原(SCR)研究了它们的催化活性。结果表明,CeO-SnO /rGO催化剂在120-280℃温度范围内表现出高SCR活性和对N的高选择性。质量比(Ce + Sn)/GO = 3.9的催化剂在160℃时NO转化率约为86%,在200-280℃温度下NO转化率高于97%,在120-280℃时N选择性高于95%。此外,该催化剂具有一定的抗SO性能。发现由于Sn掺入CeO晶格中,高度分散的CeO纳米颗粒沉积在rGO纳米片表面。CeO-SnO /rGO催化剂的介孔结构提供了大的比表面积和更多的活性位点,有利于反应物物种的吸附,从而导致高SCR活性。更重要的是,铈和锡氧化物之间的协同相互作用导致了优异的SCR活性,这使得CeSn(3.9)/rGO催化剂表面具有更高的Ce/(Ce + Ce)比、更高浓度的表面化学吸附氧和氧空位、更多的强酸位点以及更强的酸强度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77f7/9088850/0ffdc186633c/c8ra05151h-f1.jpg

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