School of Chemistry and Chemical Engineering, Hefei University of Technology, Hefei 230009, China; Anhui Province Key Laboratory of Advanced Catalytic Materials and Reaction Engineering, Hefei University of Technology, Hefei 230009, China.
School of Chemistry and Chemical Engineering, Hefei University of Technology, Hefei 230009, China.
J Environ Sci (China). 2021 Mar;101:1-15. doi: 10.1016/j.jes.2020.07.027. Epub 2020 Aug 21.
A series of MnM/palygorskite (PG) (M = La, W, Mo, Sb, Mg) catalysts was prepared by the wetness co-impregnation method for low-temperature selective catalytic reduction (SCR) of NO with NH. Conversion efficiency followed the order Sb > Mo > La > W > Mg. A combination of various physico-chemical techniques was used to investigate the influence of Sb-modified Mn/PG catalysts. MnSb/PG catalyst showed highest NO conversion at low temperatures in the presence of SO which reveals that addition of Sb oxides effectively enhances the SCR activity of catalysts. A SO step-wise study showed that MnSb/PG catalyst displays higher durable resistance to SO than Mn/PG catalyst, where the sulfating of active phase is greatly inhibited after Sb doping. Scanning electron microscopy and X-ray diffraction results showed that Sb loading enhances the dispersion of Mn oxides on the carrier surface. According to the results of characterization analyses, it is suggested that the main reason for the deactivation of Mn/PG is the formation of manganese sulfates which cause the permanent deactivation of Mn-based catalysts. For Sb-doped Mn/PG catalyst, SO ad-species formed were mainly combined with SbO rather than MnO. This preferential interaction between SbO and SO effectively shields the MnO as active species from being sulfated by SO resulting in the improvement of SO tolerance on Sb-added catalyst. Multiple information support that, owing to the addition of Sb, original formed MnO crystallite has been completely transformed into highly dispersed amorphous phase accounting for higher SCR activity.
采用等体积浸渍法制备了一系列 MnM/凹凸棒石(PG)(M=La、W、Mo、Sb、Mg)催化剂,用于 NH3 低温选择性催化还原(SCR)NO。转化率的顺序为 Sb>Mo>La>W>Mg。采用多种物理化学技术结合研究了 Sb 改性 Mn/PG 催化剂的影响。在 SO 存在下,MnSb/PG 催化剂在低温下表现出最高的 NO 转化率,表明添加 Sb 氧化物可有效提高催化剂的 SCR 活性。SO 分步研究表明,MnSb/PG 催化剂比 Mn/PG 催化剂具有更高的耐 SO2 能力,Sb 掺杂后,活性相的硫酸盐化得到了极大抑制。扫描电子显微镜和 X 射线衍射结果表明,Sb 负载增强了 Mn 氧化物在载体表面的分散性。根据表征分析结果,Mn/PG 失活的主要原因是形成了锰硫酸盐,导致 Mn 基催化剂永久性失活。对于 Sb 掺杂的 Mn/PG 催化剂,形成的 SO 吸附物种主要与 SbO 结合而不是 MnO。SbO 与 SO 之间的这种优先相互作用可有效保护 MnO 作为活性物质免受 SO2 的硫酸盐化,从而提高了添加 Sb 催化剂的抗 SO2 能力。多种信息表明,由于 Sb 的添加,原始形成的 MnO 晶相已完全转化为高度分散的无定形相,从而提高了 SCR 活性。