Abstract:In das Schichtengitter des Kaolinits kann Hydrazin reversibel eingelagert werden. Der Schichtabstand erhöht sich dabei von 7,16 Å auf 10,41 Å. Die Einlagerungsgeschwindigkeit wird wesentlich beeinflußt von den noch unbekannten Assoziationsgleichgewichten in der wässerigen Hydrazinlösung.
Eine eindimensionale FOURIER‐Projektion auf die Schichtnormale gibt einen Hinweis auf die Anordnung der Hydrazinmolekeln zwischen den Silicatschichten.
Kaoline mit den Gitterstörungen des sogenannten Fire‐Clay‐Typs reagieren m… Show more
“…After washing the intercalates with water to remove the KAc, he found that kaolinite, dickite, and hydrated halloysite reverted to their original spacings, but that nacrite formed a well-defined hydrate with d(001) equal to 8.35/~. Weiss et al (1963) reported a 8.33-/~ phase formed by the water washing of a kaolinite which had been expanded by urea but did not identify this material as a hydrated phase of kaolinite. By means of KAcand urea-intercalates, van Olphen and Deeds (1963) obtained a 8.45-.~ spacing for a well-defined hydrate of what they considered to be dickite.…”
“…After washing the intercalates with water to remove the KAc, he found that kaolinite, dickite, and hydrated halloysite reverted to their original spacings, but that nacrite formed a well-defined hydrate with d(001) equal to 8.35/~. Weiss et al (1963) reported a 8.33-/~ phase formed by the water washing of a kaolinite which had been expanded by urea but did not identify this material as a hydrated phase of kaolinite. By means of KAcand urea-intercalates, van Olphen and Deeds (1963) obtained a 8.45-.~ spacing for a well-defined hydrate of what they considered to be dickite.…”
“…With dimethyl sulphoxide (Weiss et al, 1966;Olejnik et al, 1968;Sanchez Camazano and Gonzalez Garcia, 1966) it was found that the S=O bond was perpendicular to the clay sheets with the oxygen atom 1-8 A from the plane containing the hydroxyl groups, a geometry almost identical to that found for the C = O in formamide. Pyridine N-oxide (Olejnik et al, 1970Weiss and Orth, 1973) also forms an intercalate with kaolinite and the available evidence shows that the molecule has its long axis almost perpendicular to the clay sheets with the oxygen atom at 2.0/~ from the hydroxyl plane.…”
Section: Intercalates With Other Small Moleculesmentioning
confidence: 82%
“…The N-H-9 9 O bond was found to be weaker than the N-H--9 O--C bond in liquid formamide and also the formamide molecules were shown to be at a large angle to the mineral sheets. This last point was also made by Weiss et al (1963) who used a one-dimensional Fourier projection to show that the -NH~ group was near the silicate oxygens of one sheet with the HCO group near the OH's of the neighboring layer. The essential features of the bonding between formamide and the dickite brought out by the structural evaluation were (Figures I, 2): (i) the three hydrogen bonds from the clay hydroxyls to the carbonyl oxygen, (ii) the hydrogen bond from the amide nitrogen to one of these three hydroxyls and (iii) the hydrogen bond from the amide nitrogen to the silicate oxygen of the next sheet.…”
Abstract--The recent determination of the three-dimensional crystal structure of a dickite:formamide intercalate allows insight into the clay:organic bonding schemes of amides and other small organic molecule intercalates of the kaolin minerals. It is demonstrated that the observed basal spacings of intercalates with these molecules are consistent with hydrogen bonding schemes in which, if possible, triple hydrogen bonds from the clay hydroxyls to ~( are formed. Variations in basal spacing within a series of amides can be explained by considering the maximization of hydrogen bonding while avoiding close van der Waals contacts.
“…To our knowledge, the preparation of kaolinite-CTAC complex using U as precursor was not published before. Direct intercalation of U into kaolinite was carried out using solution [1,2,4,8,9,16,20,26,28,34,37,38], mechanochemical (co-grinding) [13, 21-23, 25-28, 31, 32, 37], and homogenization [41] techniques. These techniques resulted in high degree of intercalation, but the mechanochemical and homogenization techniques require less time and consume an order of magnitude less chemicals.…”
Because of its suitability for producing kaolinite nanoscrolls, the kaolinitecetyltrimethylammonium chloride intercalation complex is of interest in the research area of kaolinite nanocomposites. Experimental and molecular simulation analyses are used to investigate this intercalation complex, revealing its real structure formed through partially methoxy-modified kaolinite. Cost-efficient homogenization method is applied to synthesize the eco-friend kaolinite-urea pre-intercalation complex, which was found to be favorable to intercalate cetyltrimethylammonium chloride into the interlayer space of kaolinite. The influence of the pre-intercalated urea molecules, the partial modification of kaolinite structure with methoxy groups, and the presence of methanol molecules in the interlayer space of kaolinite on the intercalation of cetyltrimethylammonium chloride is characterized experimentally by X-ray diffraction, thermal analysis, Fourier transform infrared spectroscopy, and electron microscopy. The kaolinite-cetyltrimethylammonium chloride complex is identified at the basal spacing of 3.82 nm with the chemical formula of Al 2 Si 2 O 5 (OH) 3.7 (OCH 3 ) 0.3 (CTAC) 1.6 (Me) 1.6 . Our molecular simulations predict methanolcontaining structures between methoxy-functionalized kaolinite layers with diffuse guest molecular arrangements.
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