An analysis of the first steps of phenol adsorption-oxidation over coprecipitated Mn-Ce catalysts: a DRIFTS study

被引:19
作者
D'alessandro, Oriana [1 ,2 ]
Thomas, Horacio J. [1 ,2 ,3 ]
Sambeth, Jorge E. [1 ,2 ]
机构
[1] UNLP CCT CONICET La Plata, Ctr Invest & Desarrollo Ciencias Aplicadas Dr Jor, RA-1900 La Plata, Argentina
[2] Fac Ciencias Exactas UNLP, RA-1900 La Plata, Argentina
[3] Planta Piloto Multiproposito PLAPIMU CICPBA, Gonnet, Argentina
关键词
Mn-Ce composite; Phenol oxidation; Phenolate; Carboxylate; Monodentate phenoxy group; MIXED-OXIDE CATALYSTS; WET OXIDATION; MANGANESE; FORMALDEHYDE; DEGRADATION; COMBUSTION; REMOVAL; SILICA; HPLC;
D O I
10.1007/s11144-012-0470-0
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
A series of Mn-Ce(M) solids (M = K or Na), with molar ratios 100-0, 50-50 and 0-100 were prepared by co-precipitation of manganese and cerium nitrate from NaOH or KOH solutions at pH = 11. In addition, part of the solids precipitated with NaOH were dried and impregnated with a Cu2+ salt. The solids were characterized by XRD, Specific Surface Area, XPS and EDS. The characterization analyses show the formation of Mn mixed oxides with different oxidation states (Mn3+, Mn4+), for samples without Ce or Mn-Ce(M) 50-50. In the latter solid and in the one where there is no Mn, the formation of CeO2 (fluorite type) was detected. The samples were tested in the phenol removal in water at 100 A degrees C and at atmospheric pressure with the aim to analyze the adsorbed species in the first stage of the adsorption-oxidation mechanisms. The results indicate, on the one hand, that [MnOx] is the active species in the process and that the most active solids are those that present (i) a higher concentration of O-I, (ii) a higher amount of Mn4+ ions. DRIFT spectroscopy showed a possible mechanism of phenol adsorption on two sites, in the first one by H interaction of OH (phenol) with an OH of the catalyst and in the second, by the formation of a phenolate species between an O (OH phenol) and Mnn+.
引用
收藏
页码:295 / 309
页数:15
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