Wetting stability of Si-MCM-41 mesoporous material in neutral, acidic and basic aqueous solutions

被引:178
作者
Landau, MV [1 ]
Varkey, SP
Herskowitz, M
Regev, O
Pevzner, S
Sen, T
Luz, Z
机构
[1] Ben Gurion Univ Negev, Dept Chem Engn, IL-84105 Beer Sheva, Israel
[2] Blechner Ctr Ind Catalysis & Proc Dev, Beer Sheva, Israel
[3] Weizmann Inst Sci, Dept Chem Phys, IL-76100 Rehovot, Israel
基金
以色列科学基金会;
关键词
Si-MCM-41; structure degradation; wetting stability;
D O I
10.1016/S1387-1811(99)00133-X
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The wetting stability of three calcined Si-MCM-41 materials synthesized at room temperature and under hydrothermal conditions with and without pH adjustment and salt addition was studied by SAXS, SEM, HR-TEM, BET-BJH, FTIR and NMR techniques. The stability was investigated after wetting with neutral, basic and acidic aqueous solutions and further recalcination. Calcined Si-MCM-41 materials synthesized at room temperature fully degraded under wetting with neutral water. Crystallization under hydrothermal conditions improved their wetting stability. pH adjustment and NaCl addition during hydrothermal crystallization led to a further improvement. It was proposed, based on spectroscopic data, that the structure degradation during wetting is caused by hydration of the siloxane structure at the wetting stage followed by siloxane hydrolysis-hydroxylation of strained Si(-OSi-)(4) units and their rearrangement-redehydroxylation during recalcination. This leads to intergrowth of curved hexagonal crystal rods, reduction of the surface area and pore volume of the material forming a disordered pore structure with increased pore walls thickness. The water-stable Si-MCM-41 synthesized with pH adjustment and salt addition was also insensitive to wetting with acidic aqueous solution. However, treatment of this non-strained material with a basic solution at pH 7.8-8.9 resulted in silica leaching and a reduction in crystallinity, the mean pore diameter and the pore volume. The rod shape and surface area remained relatively unchanged after wetting at pH 7.8. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:149 / 163
页数:15
相关论文
共 17 条
[1]   A NEW FAMILY OF MESOPOROUS MOLECULAR-SIEVES PREPARED WITH LIQUID-CRYSTAL TEMPLATES [J].
BECK, JS ;
VARTULI, JC ;
ROTH, WJ ;
LEONOWICZ, ME ;
KRESGE, CT ;
SCHMITT, KD ;
CHU, CTW ;
OLSON, DH ;
SHEPPARD, EW ;
MCCULLEN, SB ;
HIGGINS, JB ;
SCHLENKER, JL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (27) :10834-10843
[2]   Thermal and hydrothermal stability of framework-substituted MCM-41 mesoporous materials [J].
Chen, LY ;
Jaenicke, S ;
Chuah, GK .
MICROPOROUS MATERIALS, 1997, 12 (4-6) :323-330
[3]  
Choudhary VR, 1997, P INDIAN AS-CHEM SCI, V109, P229
[4]   ROOM-TEMPERATURE FORMATION OF MOLECULAR-SIEVE MCM-41 [J].
EDLER, KJ ;
WHITE, JW .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1995, (02) :155-156
[5]   ORGANIZATION OF ORGANIC-MOLECULES WITH INORGANIC MOLECULAR-SPECIES INTO NANOCOMPOSITE BIPHASE ARRAYS [J].
HUO, QS ;
MARGOLESE, DI ;
CIESLA, U ;
DEMUTH, DG ;
FENG, PY ;
GIER, TE ;
SIEGER, P ;
FIROUZI, A ;
CHMELKA, BF ;
SCHUTH, F ;
STUCKY, GD .
CHEMISTRY OF MATERIALS, 1994, 6 (08) :1176-1191
[6]   INFRARED-REFLECTANCE SPECTRA OF HEAT-TREATED, SOL-GEL-DERIVED SILICA [J].
KAMITSOS, EI ;
PATSIS, AP ;
KORDAS, G .
PHYSICAL REVIEW B, 1993, 48 (17) :12499-12505
[7]  
Kim JM, 1996, B KOR CHEM SOC, V17, P66
[8]  
KISELEV AV, 1972, INFRARED SPECTRA SUR
[9]   ORDERED MESOPOROUS MOLECULAR-SIEVES SYNTHESIZED BY A LIQUID-CRYSTAL TEMPLATE MECHANISM [J].
KRESGE, CT ;
LEONOWICZ, ME ;
ROTH, WJ ;
VARTULI, JC ;
BECK, JS .
NATURE, 1992, 359 (6397) :710-712
[10]   Application of large pore MCM-41 molecular sieves to improve pore size analysis using nitrogen adsorption measurements [J].
Kruk, M ;
Jaroniec, M ;
Sayari, A .
LANGMUIR, 1997, 13 (23) :6267-6273