Functionalization of activated carbon surface with sulfonated styrene as a facile route for solid acids preparation

被引:28
作者
Diyuk, Vitaliy E. [1 ]
Mariychuk, Ruslan T. [2 ]
Lisnyak, Vladyslav V. [1 ]
机构
[1] Kyiv Natl Taras Shevchenko Univ, Fac Chem, 64 Volodymyrska Str, UA-01601 Kiev, Ukraine
[2] Presov Univ, Dept Ecol, Fac Humanities & Nat Sci, SK-08116 Presov, Slovakia
关键词
Microporous materials; Chemical synthesis; Thermogravimetric analysis (TGA); Energy spectroscopy for chemical analysis (ESCA); Adsorption; Surface properties; MESOPOROUS CARBON; CATALYST; ESTERIFICATION; BIODIESEL; BIOCHAR; PHENOL;
D O I
10.1016/j.matchemphys.2016.09.034
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We propose a facile route for the surface functionalization of activated carbons (ACs), which are used as a solid matrix with good mechanical properties, but have the deficiency of the active surface sites to form the AC-based solid acids (ACSA) by the direct chemical method. The route includes three stages that provide active and stable strong acidic surface layer. The surface chemistry changes at the functionalization stages were controlled with thermogravimetric (TG) and thermoprogrammed desorption (TPD) methods. N-2 adsorption-desorption studies demonstrate the conservation of the AC meso- and macro-porosity. According to XPS, DRIFT, TG-TPD-IR, and potential titrimetry data, the ACSA obtained by sulfonation of the styrene functionalized AC are contained up to 1.1 mmol g(-1) of the strong acidic SO3H groups. The surface functionalization, as reported route, gives no prominent structural changes, from XRD data, the large macropores and transport channels maintain, from SEM data, and MicroRaman sp&tra show no defecting of the initial carbon matrix. The obtained ACSA are effective catalysts for the dehydration of 2-propanol and combine the high efficiency of work with the increased thermal stability of the surface layer. The thermoresistance of the ACSA significantly exceeds that of the Amberlyst-15 WET catalyst. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:138 / 145
页数:8
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