Sorption and pore condensation behavior of nitrogen, argon, and krypton in mesoporous:: MCM-48 silica materials

被引:121
作者
Thommes, M
Köhn, R
Fröba, M
机构
[1] Univ Hamburg, Inst Inorgan & Appl Chem, D-20146 Hamburg, Germany
[2] Quantachem GMBH, D-85235 Odelzhausen, Germany
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2000年 / 104卷 / 33期
关键词
D O I
10.1021/jp994133m
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
We present results of a systematic study on the sorption- and phase behavior of nitrogen, argon, and krypton at 77 and 87 K in different pristine mesoporous MCM-48 silica phases (BJH pore diameters 2-3 nm) and MCM-38 silica/iron(III) host compound, which consists of two interwoven, but unconnected three-dimensional pore systems. Different methods (e.g., BET, BJH, SF) were used to analyze nitrogen (77 K) and argon (87 K) sorption isotherms in order to characterize the MCM-48 silica materials with respect to surface area, pare volume and pore diameter. In contrast to nitrogen, argon, and krypton sorption isotherms on all MCM-48 silica materials reveal phase transitions accompanied by sorption hysteresis of type H1 (IUPAC classification) down to temperatures T well below the bulk triple-point temperature T-R, i.e., 87 K (T-R - T approximate to 28.5 K) in the case of krypton and 77 K (T-R - T approximate to 6.5 K) in the case of argon. Details of the sorption hysteresis depend on temperature and pore size, e.g., with increasing temperature and decreasing pore size a shrinkage of the hysteresis loops is observed. In contrast to the argon/MCM-48 silica system, argon sorption isotherms at T-R - T approximate to 6.5 K in controlled-pore glass of BJH pore diameter ca. 16 nm reveal no pore condensation and hysteresis, indicating that in such wide pores the pore condensation line does not extend down to this temperature for pressures up to the corresponding bulk sublimation pressure.
引用
收藏
页码:7932 / 7943
页数:12
相关论文
共 107 条
[1]   Post-synthetic preparations of titanium-containing mesopore molecular sieves [J].
Ahn, WS ;
Lee, DH ;
Kim, TJ ;
Kim, JH ;
Seo, G ;
Ryoo, R .
APPLIED CATALYSIS A-GENERAL, 1999, 181 (01) :39-49
[2]   Cubosome description of the inorganic mesoporous structure MCM-48 [J].
Alfredsson, V ;
Anderson, MW ;
Ohsuna, T ;
Terasaki, O ;
Jacob, M ;
Bojrup, M .
CHEMISTRY OF MATERIALS, 1997, 9 (10) :2066-2070
[3]   Structure of MCM-48 revealed by transmission electron microscopy [J].
Alfredsson, V ;
Anderson, MW .
CHEMISTRY OF MATERIALS, 1996, 8 (05) :1141-1146
[4]   Photocatalytic reduction of CO2 with H2O on Ti-MCM-41 and Ti-MCM-48 mesoporous zeolite catalysts [J].
Anpo, M ;
Yamashita, H ;
Ikeue, K ;
Fujii, Y ;
Zhang, SG ;
Ichihashi, Y ;
Park, DR ;
Suzuki, Y ;
Koyano, K ;
Tatsumi, T .
CATALYSIS TODAY, 1998, 44 (1-4) :327-332
[5]   Ligand-assisted liquid crystal templating in mesoporous niobium oxide molecular sieves [J].
Antonelli, DM ;
Nakahira, A ;
Ying, JY .
INORGANIC CHEMISTRY, 1996, 35 (11) :3126-3136
[6]   X-RAY-DIFFRACTION STUDY OF MESOPHASES OF CETYLTRIMETHYLAMMONIUM BROMIDE IN WATER, FORMAMIDE, AND GLYCEROL [J].
AUVRAY, X ;
PETIPAS, C ;
ANTHORE, R ;
RICO, I ;
LATTES, A .
JOURNAL OF PHYSICAL CHEMISTRY, 1989, 93 (21) :7458-7464
[7]   LIQUID-FILM INSTABILITIES IN CONFINED GEOMETRIES [J].
AWSCHALOM, DD ;
WARNOCK, J ;
SHAFER, MW .
PHYSICAL REVIEW LETTERS, 1986, 57 (13) :1607-1610
[8]   TEMPLATING OF MESOPOROUS MOLECULAR-SIEVES BY NONIONIC POLYETHYLENE OXIDE SURFACTANTS [J].
BAGSHAW, SA ;
PROUZET, E ;
PINNAVAIA, TJ .
SCIENCE, 1995, 269 (5228) :1242-1244
[9]   TEMPERATURE-DEPENDENCE OF GAS-ADSORPTION ON A MESOPOROUS SOLID - CAPILLARY CRITICALITY AND HYSTERESIS [J].
BALL, PC ;
EVANS, R .
LANGMUIR, 1989, 5 (03) :714-723
[10]   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