Birdwood kaolinite: a highly ordered kaolinite that is difficult to intercalate - an XRD, SEM and Raman spectroscopic study

被引:49
作者
Frost, RL
Van Der Gaast, SJ
Zbik, M
Kloprogge, JT
Paroz, GN
机构
[1] Queensland Univ Technol, Ctr Instrumental & Dev Chem, Brisbane, Qld 4001, Australia
[2] Netherlands Inst Sea Res, NL-1790 AB Den Burg, Netherlands
[3] Univ S Australia, Ian Wark Res Inst, Adelaide, SA 5095, Australia
关键词
acetamide; defect structure; disorder; SEM; formamide; intercalation; kaolinite; Raman spectroscopy; XRD;
D O I
10.1016/S0169-1317(01)00071-0
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
The intercalation of a highly ordered kaolinite from Birdwood, South Australia, has been studied using a combination of electron microscopy. X-ray diffraction and Raman microscopy. Highly ordered kaolinites normally intercalate easily and to a high degree. The kaolinite under study was found to intercalate acetamide and formamide with difficulty and more than IS days were required to achieve more than 20% intercalation. Further treatment did not improve the degree of intercalation past 60%. The difficulty of intercalation is attributed to the co-existence of two kaolinite phases, a highly ordered (with a Hinckley index > 1.3) and a highly disordered kaolinite, the latter material appears to coat the highly ordered kaolinite thereby limiting the intercalation. The presence of two forms of silica and a dickite were identified in the sample using X-ray diffraction. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:177 / 187
页数:11
相关论文
共 46 条
  • [21] Drift spectroscopic study of the mechanism of selective shear-flocculation of hematite from kaolinite
    Gong, WQ
    JOURNAL OF WUHAN UNIVERSITY OF TECHNOLOGY-MATERIALS SCIENCE EDITION, 1997, 12 (1-2): : 83 - 93
  • [22] DRIFT SPECTROSCOPIC STUDY OF THE MECHANISM OF SELECTIVE SHEAR-FLOCCULATION OF HEMATITE FROM KAOLINITE
    龚文琪
    Journal of Wuhan University of Technology-Materials Science, 1997, (Z1) : 83 - 93
  • [23] RAMAN-STUDY OF OH-STRETCHING VIBRATIONS IN KAOLINITE AT LOW-TEMPERATURE
    PAJCINI, V
    DHAMELINCOURT, P
    APPLIED SPECTROSCOPY, 1994, 48 (05) : 638 - 641
  • [24] Microstructural characterisation of geopolymers synthesised from kaolinite/stilbite mixtures using XRD, MAS-NMR, SEM/EDX, TEM/EDX, and HREM
    Xu, H
    Van Deventer, JSJ
    CEMENT AND CONCRETE RESEARCH, 2002, 32 (11) : 1705 - 1716
  • [25] Mid-infrared and near-infrared spectroscopic study of kaolinite-potassium acetate intercalation complex
    Zhang, Jinshan
    Cheng, Hongfei
    Liu, Qinfu
    He, Junkai
    Frost, Ray L.
    JOURNAL OF MOLECULAR STRUCTURE, 2011, 994 (1-3) : 55 - 60
  • [26] Low-temperature infrared spectroscopic study of OH-stretching modes in kaolinite and dickite
    Balan, Etienne
    Delattre, Simon
    Guillaumet, Maxime
    Salje, Ekhard K. H.
    AMERICAN MINERALOGIST, 2010, 95 (8-9) : 1257 - 1266
  • [27] THE COMBINED INELASTIC NEUTRON SCATTERING (INS) AND SOLID-STATE DFT STUDY OF HYDROGEN-ATOMS DYNAMICS IN KAOLINITE-DIMETHYLSULFOXIDE INTERCALATE
    Smrcok, L'Ubomir
    Tunega, Daniel
    Ramirez-Cuesta, Anibal Javier
    Ivanov, Alexander
    Valuchova, Jana
    CLAYS AND CLAY MINERALS, 2010, 58 (01) : 52 - 61
  • [28] XRD and Raman spectroscopic comparative study on phase transformation of γ-Al2O3 at high temperature
    Fang Ping
    He Mai
    Xie Yun-long
    Luo Meng-fei
    SPECTROSCOPY AND SPECTRAL ANALYSIS, 2006, 26 (11) : 2039 - 2042
  • [29] Modification of kaolinite surfaces through mechanochemical treatment -: a mid-IR and near-IR spectroscopic study
    Frost, RL
    Makó, É
    Kristóf, J
    Kloprogge, JT
    SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2002, 58 (13) : 2849 - 2859
  • [30] Operando XAS/XRD and Raman Spectroscopic Study of Structural Changes of the Iron Molybdate Catalyst during Selective Oxidation of Methanol
    Gaur, Abhijeet
    Schumann, Max
    Raun, Kristian Viegaard
    Stehle, Matthias
    Beato, Pablo
    Jensen, Anker Degn
    Grunwaldt, Jan-Dierk
    Hoj, Martin
    CHEMCATCHEM, 2019, 11 (19) : 4871 - 4883