A low-defect kaolinite of 7.18-Γ basal spacing was expanded upon intercalation with hydrazine. The 001 d-spacing was broad and the peak resolved into components at 10.28, 9.48, and 8.80 Γ . It was found that the ordered kaolinite predominantly expanded to 9.48 Γ with 31.2% and 10.28 Γ with 38.0% of t
The Role of Water in the Intercalation of Kaolinite with Potassium Acetate
β Scribed by Ray L. Frost; Janos Kristof; Gina N. Paroz; Thu Ha Tran; J.Theo Kloprogge
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- English
- Weight
- 165 KB
- Volume
- 204
- Category
- Article
- ISSN
- 0021-9797
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β¦ Synopsis
Water in intercalated kaolinites is observed first as bands inthe hydroxyl-stretching region at 3300 to 3550 cm-1 and bythe water H-O-H bending vibrations in the 1560 to 1680-cm-1 region. For potassium-acetate-intercalated kaolinite, hydroxyl-stretching bands attributed to water are observed at approximately 3540, approximately 3475, approximately 3430, and approximately 3380 cm-1. Water bending modes areobserved at 1560, 1586, 1610, and 1679 cm-1. These bands are attributed to (a) water molecules adsorbed on the kaolinite surface, (b) zeolitic water, (c) molecular first layer water, and (d) orderedwater on the hydroxyl surface, respectively. The intensities ofthe bands are a function of the method of preparation of the intercalated kaolinite. As the kaolinite was washed for varying time intervals, the 1560 cm-1 band decreased in intensity more rapidly than the 1610 cm-1 band. Even after washing for 24 h significant concentrations of water remained on the kaolinite and only heating removed the water. The 1560, 1586, and 1610 cm-1 bands are attributed (a) to free or non-hydrogen-bonded water held in the interlayer spaces of the kaolinite, (b) to water in the hydration sphere of the potassium ion, and (c) to surface-adsorbed water on the kaolinite layers. In kaolinites intercalated under pressure, an additional band was observed at 1679 cm-1. It is proposed that this band is due to water coordinated to the kaolinite surface. Copyright 1998 Academic Press.
π SIMILAR VOLUMES
The modification of kaolinite hydroxyl surfaces of both ordered and disordered kaolinites has been studied under a range of conditions and intercalating agents. This has been achieved by the study of the kaolinite hydroxyl deformation vibrations by the application of diffuse reflectance Fourier tran
Kaolinite hydroxyl surfaces have been modified upon intercalation with potassium acetate under a range of conditions. Modification is observed by changes in the hydroxyl stretching region using Raman and infrared spectroscopy. Upon the intercalation of low defect kaolinite with potassium acetate und
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