Study of the structural evolutions of mesoporous MCM-48 silica infiltrated with carbon by different techniques

被引:20
作者
Parmentier, J
Vix-Guterl, C
Gibot, P
Reda, M
Ilescu, M
Werckmann, J
Patarin, J
机构
[1] Univ Haute Alsace, Ecole Natl Super Chim Mulhouse, Lab Mat Min, CNRS,UMR 7016, F-68093 Mulhouse, France
[2] CNRS, UMR 9069, Inst Chim Surfaces & Interfaces, F-68057 Mulhouse, France
[3] CNRS, UMR 7504, Inst Phys & Chim Mat, F-67037 Strasbourg, France
关键词
MCM-48; thermal stability; porogen agent; carbon infiltration processes;
D O I
10.1016/S1387-1811(03)00396-2
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The physico-chemical properties of ordered mesoporous carbons obtained by a negative replication process are strongly influenced by their preparations. In order to get a better understanding of the carbon formation, the structural evolution of the mesoporous MCM-48 silica templates before and after C infiltration by two different processes (and a subsequent oxidation), was studied using various techniques such as XRD, N-2 adsorption/desorption and TEM. It was shown that the use of a liquid carbon precursor such as a sucrose solution led to a strong alteration of the silica template (loss of long-range ordering, disappearance of the narrow mesopore size distribution). This was attributed to (i) the high temperature of the process (1173 K) and (ii) to the water vapor released during the carbonization that hydrolysed the poorly hydrothermally stable silica network. On the contrary, the pyrolytic decomposition of a gaseous carbon precursor such as propylene, performed at lower temperature (1023 K) and without water release, only led to minor modifications. These behaviors may influence the physico-chemical properties of the resulting carbon. For both impregnation processes, carbon acts as a highly stable porogene agent. Heat-treatment at a temperature as high as 1473 K in an inert atmosphere and a subsequent oxidation for the removal of the carbon succeeded in preserving the long-range ordering of the starting silica template and its surface area. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:87 / 96
页数:10
相关论文
共 25 条
[1]   THE DETERMINATION OF PORE VOLUME AND AREA DISTRIBUTIONS IN POROUS SUBSTANCES .1. COMPUTATIONS FROM NITROGEN ISOTHERMS [J].
BARRETT, EP ;
JOYNER, LG ;
HALENDA, PP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1951, 73 (01) :373-380
[2]  
BRINKER CJ, 1990, SOL GEL SCI PHYSICS, P680
[3]   Adsorption of gases in multimolecular layers [J].
Brunauer, S ;
Emmett, PH ;
Teller, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1938, 60 :309-319
[4]  
BUNAUER S, 1940, J AM CHEM SOC, V62, P1723
[5]  
Carrott MMLR, 2000, LANGMUIR, V16, P9103
[6]  
Carrott MMLR, 1999, LANGMUIR, V15, P8895
[7]   A detailed study of thermal, hydrothermal, and mechanical stabilities of a wide range of surfactant assembled mesoporous silicas [J].
Cassiers, K ;
Linssen, T ;
Mathieu, M ;
Benjelloun, M ;
Schrijnemakers, K ;
Van Der Voort, P ;
Cool, P ;
Vansant, EF .
CHEMISTRY OF MATERIALS, 2002, 14 (05) :2317-2324
[8]  
HENCH LL, 1990, CHEM REV, V90, P59
[9]   Synthesis of ordered mesoporous carbon molecular sieves CMK-1 [J].
Joo, SH ;
Jun, S ;
Ryoo, R .
MICROPOROUS AND MESOPOROUS MATERIALS, 2001, 44 :153-158
[10]   Structural study of mesoporous MCM-48 and carbon networks synthesized in the spaces of MCM-48 by electron crystallography [J].
Kaneda, M ;
Tsubakiyama, T ;
Carlsson, A ;
Sakamoto, Y ;
Ohsuna, T ;
Terasaki, O ;
Joo, SH ;
Ryoo, R .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (06) :1256-1266