(C3H6O2)2(SI6O12)2, A NEW SILICA SODALITE SYNTHESIZED, USING 1,3-DIOXOLANE AS TEMPLATE

被引:26
作者
VANDEGOOR, G [1 ]
BEHRENS, P [1 ]
FELSCHE, J [1 ]
机构
[1] UNIV KONSTANZ, FAK CHEM, D-78434 CONSTANCE, GERMANY
来源
MICROPOROUS MATERIALS | 1994年 / 2卷 / 06期
关键词
CLATHRASIL; TEMPLATE; HOST-GUEST INTERACTION; SODALITE; PHASE TRANSITION;
D O I
10.1016/0927-6513(94)E0064-2
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A clathrasil with SOD structure has been obtained using 1,3-dioxolane as a template. The synthesis was achieved under hydrothermal conditions at temperatures between 423 and 433 K in the SiO2-Na2O-C3H6O2-H2O system. The choice of the template was guided by stereochemical comparisons with the templates known for silica sodalite synthesis, ethylene glycol and 1,3,5-trioxane. The powder X-ray diffraction (XRD) measurement of dioxolane silica sodalite (C3H6O2)2(Si6O12)2 showed the typical pattern of silica sodalites with sharp, discrete reflections indicating high crystallinity. Indexing and refinement of the diffraction pattern gave a body-centered cubic unit cell with a lattice constant a0 = 8.868 (1) angstrom at room temperature, which is significantly larger than previously found in other silica sodalites. The value of a0 agrees with the Si-O-Si bonding angle derived from the position of the Si-29 NMR signal. Infrared (IR) and H-1, C-13 nuclear magnetic resonance (NMR) spectroscopic data are in agreement with dioxolane molecules occluded in a porous matrix. The weight loss during thermal analysis in an oxygen atmosphere shows that within the limits of the method each sodalite cage is occupied by one 1,3-dioxolane molecule. Differential scanning calorimetry (DSC) between 120 and 470 K reveals a reversible, temperature-induced phase transition at 271 K.
引用
收藏
页码:493 / 500
页数:8
相关论文
共 41 条
[1]  
ALMOND MJ, 1989, ADV SPECTOS, V17
[2]   SPECTRA OF ACETALS .1. THE INFRARED AND RAMAN SPECTRA OF 1-3-DIOXOLAN [J].
BARKER, SA ;
BOURNE, EJ ;
PINKARD, RM ;
WHIFFEN, DH .
JOURNAL OF THE CHEMICAL SOCIETY, 1959, (FEB) :802-806
[3]  
Barrer R. M., 1982, HYDROTHERMAL CHEM ZE
[4]   MODELING THE SIMILARITIES AND DIFFERENCES BETWEEN THE SODALITE CAGES (BETA-CAGES) IN THE GENERIC MATERIALS - SODALITE, ZEOLITES OF TYPE-A, AND ZEOLITES WITH FAUJASITE FRAMEWORKS [J].
BEAGLEY, B ;
TITILOYE, JO .
STRUCTURAL CHEMISTRY, 1992, 3 (06) :429-448
[5]  
BEHRENS P, UNPUB
[6]   SYNTHESIS OF SILICA-SODALITE FROM NON-AQUEOUS SYSTEMS [J].
BIBBY, DM ;
DALE, MP .
NATURE, 1985, 317 (6033) :157-158
[7]  
BIBBY DM, 1989, ACS SYM SER, V398, P209
[8]   A PROPOSAL FOR A MECHANISM OF NUCLEATION IN ZEOLITE SYNTHESIS [J].
BRUNNER, GO .
ZEOLITES, 1992, 12 (04) :428-430
[9]   REMARKS ON SYMMETRIES OCCURRING IN THE SODALITE FAMILY [J].
DEPMEIER, W .
ZEITSCHRIFT FUR KRISTALLOGRAPHIE, 1992, 199 (1-2) :75-89
[10]   TETRAGONAL TETRAHEDRA DISTORTIONS IN CUBIC SODALITE FRAMEWORKS [J].
DEPMEIER, W .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 1984, 40 (JUN) :185-191