溶剂热法制备同时脱除1,2-二氯苯和呋喃的锰基催化剂

Juan Qiu, Yaqi Peng, Minghui Tang, Shengyong Lu, Xiaodong Li, Jianhua Yan
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引用次数: 3

摘要

本研究采用溶剂热法合成了锰基双金属氧化物催化剂。不同的金属(Ce、Co和Fe)对催化剂的物理化学性质有很大的影响,导致催化剂同时去除1,2-二氯苯(1,2- dcb)和呋喃的催化活性不同,作为多氯二苯并二苯并呋喃(PCDD/Fs)的模型。Fe-MnOx表现出最好的催化活性,在240℃下对1,2- dcb的去除率为62%,对呋喃的去除率为100%。采用了Brunauer-Emmett-Teller (BET)、x射线衍射(XRD)、扫描电镜(SEM)、x射线光电子能谱(XPS)、H2程序升温还原(H2- tpr)、氨程序升温脱附(NH3-TPD)等分析技术。与纯MnOx催化剂相比,Fe-MnOx具有更高的比表面积(117.9 m2/g)。SEM观察显示Fe-MnOx呈花状纳米片结构。XPS分析表明,Mn4+/Mn3+和活性氧在1,2- dcb和呋喃的催化氧化中起关键作用。考察了锰基双金属氧化物催化剂对1,2- dcb和呋喃的氧化活性、选择性和稳定性。1,2- dcb与呋喃之间存在竞争,使得呋喃的吸附先于1,2- dcb发生。
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Solvothermal preparation of Mn-based catalysts for simultaneous removal of 1,2-dichlorobenzene and furan

In this study, Mn-based bimetallic oxide catalysts were synthesized via the solvothermal method. Different metals (Ce, Co and Fe) exhibited a great impact on the physicochemical properties of catalysts, resulting in different catalytic activities for the simultaneous removal of 1,2-dichlorobenzene (1,2-DCB) and furan, as a model of polychlorinated dibenzodioxins and dibenzo-furans (PCDD/Fs). Fe–MnOx presented the best catalytic activity, with a removal efficiency of 62% for 1,2-DCB and 100% for furan at 240 °C. Several analytical techniques were employed, namely, Brunauer–Emmett–Teller (BET), X-ray diffraction (XRD), scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS), H2 temperature-programmed reduction (H2-TPR), and ammonia temperature programmed desorption (NH3-TPD). Compared with pure MnOx catalysts, Fe–MnOx shows a higher specific surface area of 117.9 m2/g. SEM observations showed flower-like nanosheet structures for Fe–MnOx. XPS analysis indicated that Mn4+/Mn3+ and active oxygen play the key roles in the catalytic oxidation of 1,2-DCB and furan. The catalytic activity, selectivity and stability of Mn-based bimetallic oxide catalysts for the oxidation of 1,2-DCB and furan were tested. Competition exists between 1,2-DCB and furan such that the adsorption of furan occurs prior to 1,2-DCB.

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