Catalytical studies on trimethylsilylated Ti-MCM-41 and Ti-MCM-48 materials

被引:58
作者
Igarashi, Naoko
Hashimoto, Kazuhito
Tatsumi, Takashi
机构
[1] Univ Tokyo, Adv Sci & Technol Res Ctr, Meguro Ku, Tokyo 1538904, Japan
[2] Tokyo Inst Technol, Midori Ku, Div Catalyt Chem, Chem Resources Lab,Midori Ku, Yokohama, Kanagawa 2268503, Japan
关键词
Ti-MCM-41; Ti-MCM-48; hydrophobicity; trimethylsilylation; epoxidation catalyst;
D O I
10.1016/j.micromeso.2007.02.041
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Titanium-incorporated MCM-41 and MCM-48 materials (Ti-MCM-41 and Ti-MCM-48, respectively) have been trimethylsilylated by employing various silylating agents (i.e., hexamethyldisilazane (HMDZ) and trimethylchlorosilane (TMCS) in toluene, and a mixture of TMCS and hexametyldisiloxane (HMDS)). Their catalytic activities in various oxidation reactions as well as their physical properties are compared. The highly reactive HMDZ has achieved the maximum degree of silylation to introduce 2.35 and 2.06 trimethylsilyl groups per 1 nm(2) on the surface of Ti-MCM-41 and -48, respectively. IR spectra have confirmed that HMDZ can react with hydrogen-bonded silanol groups as well as isolated silanol groups, generating a new band at 3700 cm(-1) while TMCS does not. These silylated materials show remarkably high catalytic activity in the oxidation of substrates with various molecular sizes (from C-6 to C-12) with H2O2 and tert-butyl hydroperoxide (TBHP) compared to non-silylated samples. Introducing a small amount of H2O so as to double the H2O content in a reaction system for the oxidation of cyclododecene using TBHP has approximately doubled the catalytic activity. Such unexpected results were only observed with highly hydrophobic samples, Furthermore, by conducting the reaction at 343 K for 6 h over highly silylated Ti-MCM-48, high conversion of 98% has been attained. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:269 / 280
页数:12
相关论文
共 39 条
[1]   Surface characterization and functionalization of MCM-41 silicas via silazane silylation [J].
Anwander, R ;
Nagl, I ;
Widenmeyer, M ;
Engelhardt, G ;
Groeger, O ;
Palm, C ;
Röser, T .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (15) :3532-3544
[2]  
Anwander R, 1998, STUD SURF SCI CATAL, V117, P135
[3]   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
[4]   Organically modified titanium-rich Ti-MCM-41, efficient catalysts for epoxidation reactions [J].
Bhaumik, A ;
Tatsumi, T .
JOURNAL OF CATALYSIS, 2000, 189 (01) :31-39
[5]   SYNTHESIS, CHARACTERIZATION, AND CATALYTIC ACTIVITY OF TI-MCM-41 STRUCTURES [J].
BLASCO, T ;
CORMA, A ;
NAVARRO, MT ;
PARIENTE, JP .
JOURNAL OF CATALYSIS, 1995, 156 (01) :65-74
[6]   Improvement in hydrophobicity of Ti-MCM-41 using a new silylation agent MSTFA [J].
Bu, J ;
Rhee, HK .
CATALYSIS LETTERS, 2000, 65 (1-3) :141-145
[7]   Silylation of Ti-MCM-41 by trimethylsilyl-imidazole and its effect on the olefin epoxidation with aqueous H2O2 [J].
Bu, J ;
Rhee, HK .
CATALYSIS LETTERS, 2000, 66 (04) :245-249
[8]  
Chen JS, 1995, ANGEW CHEM INT EDIT, V34, P2694
[9]   OXIDATION OF OLEFINS WITH HYDROGEN-PEROXIDE AND TERT-BUTYL HYDROPEROXIDE ON TI-BETA CATALYST [J].
CORMA, A ;
ESTEVE, P ;
MARTINEZ, A ;
VALENCIA, S .
JOURNAL OF CATALYSIS, 1995, 152 (01) :18-24
[10]   ACTIVITY OF TI-BETA CATALYST FOR THE SELECTIVE OXIDATION OF ALKENES AND ALKANES [J].
CORMA, A ;
CAMBLOR, MA ;
ESTEVE, P ;
MARTINEZ, A ;
PEREZPARIENTE, J .
JOURNAL OF CATALYSIS, 1994, 145 (01) :151-158