Strategies for immobilization of manganese on expanded natural clays: Catalytic activity in the CWPO of methyl orange

被引:27
作者
Alejandro Galeano, Luis [1 ,3 ]
Gil, Antonio [2 ]
Angel Vicente, Miguel [3 ]
机构
[1] Univ Narino, Dept Quim, Grp Invest Mat Func & Catalisis GIMFC, Pasto, Colombia
[2] Univ Publ Navarra, Dept Quim Aplicada, Pamplona 31006, Spain
[3] Univ Salamanca, Fac Ciencias Quim, Dept Quim Inorgan, E-37008 Salamanca, Spain
关键词
Al/Mn-pillared clay; MnS cluster; Azo-dye methyl orange; CWPO; WET PEROXIDE OXIDATION; PILLARED CLAYS; TRANSITION-METAL; AZO-DYE; REDUCTIVE DISSOLUTION; HYDROGEN-PEROXIDE; PHOTOSYSTEM-II; AL-FE; PHENOL; ACID;
D O I
10.1016/j.apcatb.2011.03.023
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The efficiency of the immobilization of manganese on natural bentonite has been studied by the comparison of three methods: (i) pillaring with Al-13 followed by wet impregnation with aqueous manganese nitrate, (ii) pillaring with a mixed Al/Mn oligomeric solution and thermal treatment, and (iii) Mn2+-homoionization of the starting clay and subsequent in situ generation of MnS clusters by H2S gas treatment. The resulting solids were characterized by atomic absorption spectroscopy (AAS), cationic exchange capacity (CEC), powder X-ray diffraction (XRD), scanning electron microscopy/energy dispersive X-ray analysis (SEM-EDX), nitrogen adsorption at 196 degrees C and thermal analysis (DSC/TGA). Catalytic assessment of the materials was made in the Wet Peroxide Oxidation (CWPO) of the azo-dye methyl orange in aqueous solution at room temperature and atmospheric pressure. The in situ generation of the intercalated MnS clusters was shown to be the most efficient method for the metal incorporation in the interlayer of the hosting aluminosilicate. The solids obtained by this method resulted to be stable against the chemical leaching of the metal as well as the most active to catalyze the CWPO reaction under very mild conditions of temperature, pressure and pH (18 degrees C, 0.7 atm and 7.5). (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:252 / 260
页数:9
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