Oxidation of H2S on activated carbon KAU and influence of the surface state

被引:56
作者
Brazhnyk, Dmitrii V.
Zaitsev, Yuri P.
Bacherikova, Irina V.
Zazhigalov, Valery A.
Stoch, Jerzy
Kowal, Andrzey
机构
[1] Natl Acad Sci Ukraine, Inst Sorpt & Problems Endocrinol, Ukranian Polish Lab Catalysis, Kiev, Ukraine
[2] Polish Acad Sci, Inst Catalysis & Surface Chem, PL-30239 Krakow, Poland
关键词
hydrogen sulfides; selective oxidation; activated carbon;
D O I
10.1016/j.apcatb.2005.12.028
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
Properties of the oxidized activated carbon KAU treated at different temperatures in inert atmosphere were studied by means of DTA, Boehm titration, XPS and AFM methods and their catalytic activity in H2S oxidation by air was determined. XPS analysis has shown the existence of three types of oxygen species on carbon catalysts surface. The content of oxygen containing groups determined by Boehm titration is correlated with their amount obtained by XPS. Catalytic activity of the KAU catalysts in selective oxidation of hydrogen sulfide is connected with chemisorbed charged oxygen species (O-3.1 oxygen type with BE 536.8-537.7 eV) present on the carbons surface. Formation of dense sulfur layer (islands of sulfur) on the carbons surface and removal of active oxygen species are the reason of the catalysts deactivation in H,S selective oxidation. The treatment of deactivated catalyst in inert atmosphere at 300 degrees C gives full regeneration of the catalyst activity at low temperature reaction but only its partial reducing at high reaction temperature. The last case is connected with transformation of chemisorbed charged oxygen species into C=O groups. The KAU samples treated in flow of inert gas at 900-1000 degrees C were very active in H2S oxidation to elemental sulfur transforming up to 5 157 mmol H2S/g catalyst at 180 degrees C with formation of 1.7-1.9 g S-x/g catalyst. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:557 / 566
页数:10
相关论文
共 62 条
[1]   Effect of pH and surface chemistry on the mechanism of H2S removal by activated carbons [J].
Adib, F ;
Bagreev, A ;
Bandosz, TJ .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1999, 216 (02) :360-369
[2]   Effect of surface characteristics of wood-based activated carbons on adsorption of hydrogen sulfide [J].
Adib, F ;
Bagreev, A ;
Bandosz, TJ .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1999, 214 (02) :407-415
[3]   XPS SIMS STUDY ON THE SURFACE-CHEMISTRY OF COMMERCIALLY AVAILABLE ACTIVATED CARBONS USED AS CATALYST SUPPORTS [J].
ALBERS, P ;
DELLER, K ;
DESPEYROUX, BM ;
SCHAFER, A ;
SEIBOLD, K .
JOURNAL OF CATALYSIS, 1992, 133 (02) :467-478
[4]   SURFACE-CHEMISTRY OF CARBON - ACTIVATION OF MOLECULAR-OXYGEN [J].
ATAMNY, F ;
BLOCKER, J ;
DUBOTZKY, A ;
KURT, H ;
TIMPE, O ;
LOOSE, G ;
MAHDI, W ;
SCHLOGL, R .
MOLECULAR PHYSICS, 1992, 76 (04) :851-886
[5]   On the mechanism of hydrogen sulfide removal from moist air on catalytic carbonaceous adsorbents [J].
Bagreev, A ;
Bandosz, TJ .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2005, 44 (03) :530-538
[6]   A role of sodium hydroxide in the process of hydrogen sulfide adsorption/oxidation on caustic-impregnated activated carbons [J].
Bagreev, A ;
Bandosz, TJ .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2002, 41 (04) :672-679
[7]   pH of activated carbon surface as an indication of its suitability for H2S removal from moist air streams [J].
Bagreev, A ;
Adib, F ;
Bandosz, TJ .
CARBON, 2001, 39 (12) :1897-1905
[8]   Effect of pore structure and surface chemistry of virgin activated carbons on removal of hydrogen sulfide [J].
Bandosz, TJ .
CARBON, 1999, 37 (03) :483-491
[9]  
Boehm H.P., 1966, CHEM IDENTIFICATION, V16,, P179, DOI [10.1016/S0360-0564(08)60354-5, DOI 10.1016/S0360-0564(08)60354-5]
[10]  
BOLOTIN AB, 1988, ZH STRUKT KHIM, V29, P19