Qin Caihong, Huang Xuemin, Dang Xiaoqing, Huang Jiayu, Teng Jingjing, Kang Zhongli
School of Environmental and Municipal Engineering, Xi'an University of Architecture and Technology, No. 13 Yanta Road, Xi'an, Shaanxi 710055, PR China.
School of Environmental and Municipal Engineering, Xi'an University of Architecture and Technology, No. 13 Yanta Road, Xi'an, Shaanxi 710055, PR China.
Chemosphere. 2016 Nov;162:125-30. doi: 10.1016/j.chemosphere.2016.07.085. Epub 2016 Aug 2.
A series of Ag-Mn/γ-Al2O3 were prepared under different Ag/Mn impregnation sequence and tested in the sequential adsorption-plasma catalytic removal of toluene. When Mn was impregnated first, the resulting catalyst, Ag-Mn(F)/γ-Al2O3, had longer breakthrough time, gave less emission of toluene, had higher CO2 selectivity, and had better carbon balance and COx yield compared to catalysts prepared via other impregnation sequences. After 120 min of NTP treatment, the carbon balance of Ag-Mn(F)/γ-Al2O3 was 91%, with 87% as COx contributions. A Brunauer-Emmett-Teller (BET) analysis and X-ray photoelectron spectroscopy (XPS) results show that, the impregnation sequence impacts the BET surface area and the ratio and existing state of Ag on the surface of the catalysts. The longer breakthrough time when using Ag-Mn(F)/γ-Al2O3 as catalyst is attributed to the large amount of Ag(+) on the surface. Ag(+) is a new active site for toluene adsorption. When Ag was impregnated first (Ag(F)-Mn/γ-Al2O3) or Ag and Mn co-impregnated (Ag-Mn-C/γ-Al2O3), the predominant specie was Ag(+). Both Ag(0) and Ag(+) species were detected on Ag-Mn(F)/γ-Al2O3. Ag(0) cooperation with MnOx may promote the migration of surface active oxygen. This would facilitate the oxidation of adsorbed toluene with CC bond already weakened by Ag(+) and would result in higher CO2 selectivity and better carbon balance as seen in the Ag-Mn(F)/γ-Al2O3 system.
通过不同的银/锰浸渍顺序制备了一系列Ag-Mn/γ-Al₂O₃,并用于甲苯的顺序吸附-等离子体催化去除测试。当先浸渍锰时,所得催化剂Ag-Mn(F)/γ-Al₂O₃与通过其他浸渍顺序制备的催化剂相比,具有更长的穿透时间、更低的甲苯排放、更高的二氧化碳选择性以及更好的碳平衡和一氧化碳生成率。在非热等离子体(NTP)处理120分钟后,Ag-Mn(F)/γ-Al₂O₃的碳平衡为91%,其中87%以一氧化碳的形式贡献。布鲁诺尔-埃米特-泰勒(BET)分析和X射线光电子能谱(XPS)结果表明,浸渍顺序会影响催化剂的BET表面积以及银在催化剂表面的比例和存在状态。使用Ag-Mn(F)/γ-Al₂O₃作为催化剂时较长的穿透时间归因于其表面大量的Ag(+)。Ag(+)是甲苯吸附的新活性位点。当先浸渍银(Ag(F)-Mn/γ-Al₂O₃)或银和锰共浸渍(Ag-Mn-C/γ-Al₂O₃)时,主要物种是Ag(+)。在Ag-Mn(F)/γ-Al₂O₃上同时检测到Ag(0)和Ag(+)物种。Ag(0)与氧化锰的协同作用可能促进表面活性氧的迁移。这将有利于氧化已被Ag(+)削弱了碳碳键的吸附甲苯,从而导致如Ag-Mn(F)/γ-Al₂O₃体系中更高的二氧化碳选择性和更好的碳平衡。