Physicochemical characterization of silicalite-1 nanophase material

被引:174
作者
Ravishankar, R
Kirschhock, C
Schoeman, BJ
Vanoppen, P
Grobet, PJ
Storck, S
Maier, WF
Martens, JA
De Schryver, FC
Jacobs, PA
机构
[1] Katholieke Univ Leuven, Ctr Oppervlaktechem & Katalyse, Dept Interfasechem, B-3001 Heverlee, Belgium
[2] Lulea Univ Technol, Dept Chem Technol, Lulea, Sweden
[3] Katholieke Univ Leuven, Lab Mol Dynam & Spect, B-3001 Heverlee, Belgium
[4] Max Planck Inst Kohlenforsch, Mulheim, Germany
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 1998年 / 102卷 / 15期
关键词
D O I
10.1021/jp973147u
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
A silicalite-1 nanophase material with an elementary particle size of 18-100 nm is synthesized from clear solution and isolated and purified using supercentrifugation. The nanopowder is characterized in detail using scanning electron microscopy, high-resolution transmission electron microscopy, attenuated force microscopy, Si-29 magic angle spinning NMR, C-13 cross polarization magic angle spinning NMR, X-ray diffraction, dinitrogen physisorption, and thermogravimetric analysis and compared with micrometer-sized silicalite-1. The nanosized and micrometer-sized materials have many common properties including the refined structure and the nature and concentrations of tetrapropylammonium species incorporated during the synthesis. Unique properties of the nanophase are a splitting of the characteristic framework vibration at 550 cm(-1) into a doublet at 555 and 570 cm(-1), a high concentration of defect sites, and a strain in the crystallites along the "a" crystallographic direction. The nanophase exhibits a two-stage dinitrogen physisorption in the low-pressure region, ascribed to adsorptions in micropores created by the stacking of the nanoparticles in addition to adsorptions in the intracrystalline micropores.
引用
收藏
页码:2633 / 2639
页数:7
相关论文
共 49 条
  • [1] Barrer RM., 1982, HYDROTHERMAL CHEM ZE
  • [2] FACTORS GOVERNING THE SYNTHESIS OF ZEOLITES FROM SILICOALUMINATE HYDROGELS - A COMPARATIVE-STUDY OF THE CRYSTALLIZATION MECHANISMS OF ZEOLITES-Y, MORDENITE AND ZSM-5
    BODART, P
    NAGY, JB
    GABELICA, Z
    DEROUANE, EG
    [J]. JOURNAL DE CHIMIE PHYSIQUE ET DE PHYSICO-CHIMIE BIOLOGIQUE, 1986, 83 (11-12) : 777 - 790
  • [3] A HIGH-RESOLUTION SOLID-STATE SI-29 NMR-STUDY OF ZSM-5 TYPE ZEOLITES
    BOXHOORN, G
    KORTBEEK, AGTG
    HAYS, GR
    ALMA, NCM
    [J]. ZEOLITES, 1984, 4 (01): : 15 - 21
  • [4] AN INVESTIGATION INTO THE STRUCTURE AND POSITION OF ORGANIC-BASES IN ZSM-5-TYPE ZEOLITES BY HIGH-RESOLUTION SOLID-STATE C-13 NMR-SPECTROSCOPY
    BOXHOORN, G
    VANSANTEN, RA
    VANERP, WA
    HAYS, GR
    HUIS, R
    CLAGUE, D
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1982, (04) : 264 - 265
  • [5] Adsorption of gases in multimolecular layers
    Brunauer, S
    Emmett, PH
    Teller, E
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1938, 60 : 309 - 319
  • [6] KINETICS OF ZEOLITE A CRYSTALLIZATION
    CIRIC, J
    [J]. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1968, 28 (02) : 315 - &
  • [7] Low-temperature synthesis and characterization of a stable colloidal TPA-silicalite-1 suspension
    Corkery, RW
    Ninham, BW
    [J]. ZEOLITES, 1997, 18 (5-6): : 379 - 386
  • [8] USES OF IR SPECTROSCOPY IN IDENTIFYING ZSM ZEOLITE STRUCTURE
    COUDURIER, G
    NACCACHE, C
    VEDRINE, JC
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1982, (24) : 1413 - 1415
  • [9] DIRECT MEASUREMENTS OF THE CRYSTAL-GROWTH RATE AND NUCLEATION BEHAVIOR OF SILICALITE, A ZEOLITIC SILICA POLYMORPH
    CUNDY, CS
    LOWE, BM
    SINCLAIR, DM
    [J]. JOURNAL OF CRYSTAL GROWTH, 1990, 100 (1-2) : 189 - 202
  • [10] HOMOGENEOUS VERSUS HETEROGENEOUS ZEOLITE NUCLEATION
    DOKTER, WH
    VANGARDEREN, HF
    BEELEN, TPM
    VANSANTEN, RA
    BRAS, W
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1995, 34 (01): : 73 - 75