Diffraction patterns products

Stmctural order varies from x-ray indifferent (amorphous) to some degree of crystallinity. The latter product has been named pseudoboehmite or gelatinous boehmite. Its x-ray diffraction pattern shows broad bands that coincide with the strong reflections of the weU-crystallized boehmite. 

Lastochkina et al. [216] reported on the preparation of KTaOi.5F3-H20, but the X-ray powder diffraction pattern obtained for the anhydrous product, KTaOi.5F3, does not correspond with the pattern given for K2Ta203F6 in [215]. 

The dichlorodibenzo-p-dioxin component was isolated by passing a dioxane solution of the mixture through acetate ion exchange resin to remove phenolics. The eluted product was recrystallized from benzene. The x-ray powder diffraction pattern of the precipitate was identical with that of 2,7-dichlorodibenzo-p-dioxin. Analysis of the mother liquor by GLC showed a singular peak consistent with 2,7-dichlorodibenzo-p-dioxin. The mother liquor was cooled to 5°C and yielded transparent crystals. This material had an x-ray diffraction pattern congruent to a sample of 2,8-dichlorodibenzo-p-dioxin obtained from A. E. Pohland (FDA). The two patterns were quite distinct from each other 14, 15). 

A room temperature powder X-ray diffraction pattern for Na8[GaSi04]6(C104)2 Sodalite with Si as an internal standard for phase identification in the reaction products has been studied. X-ray powder diffraction study confirms the cubic structure of Na8[GaSi04]6(C104)2 sodalite synthesized... 

Fig. 1. The x-ray diffraction patterns of hydrolytic precipitation products of Al, showing how four different organic acids influence the transformation to more crystalline phases. The initial Al concentration was l.lxl 0 3M at an OH/A1 molar ratio of 3 and the solution was aged for 40 d at room temperature in the presence of 10 4M organic acid (Kwong and Huang 1979b).

X-ray powder diffractometry can be used to study solid state reactions, provided the powder pattern of the reactant is different from that of the reaction product. The anhydrous and hydrated states of many pharmaceutical compounds exhibit pronounced differences in their powder x-ray diffraction patterns. Such differences were demonstrated earlier in the case of fluprednisolone and carbamazepine. Based on such differences, the dehydration kinetics of theophylline monohydrate (CvHgN H20) and ampicillin trihydrate (Ci6H19N304S 3H2O) were studied [66]. On heating, theophylline monohydrate dehydrated to a crystalline anhydrous phase, while the ampicillin trihydrate formed an amorphous anhydrate. In case of theophylline, simultaneous quantification of both the monohydrate and the anhydrate was possible. It was concluded that the initial rate of this reaction was zero order. By carrying out the reaction at several... 

The identities of the products were confirmed by infrared spectroscopy and x-ray powder diffraction patterns. Physical data on the inorganic tin additives studied are given in Table II. 

The method is limited however to the vacuum region <10-3 torr. Standard deviations of the temperature in the order of +5 °K and 1 °K were found at 1225 °K and at 300 °K respectively. This same method was also used by Wiedemann44 to follow continuously the evolution of gaseous decomposition products with simultaneous recording of the heating X-ray45 diffraction pattern (TMBA-X-ray method). 

A possible economically attractive alternative would be the production of acrylic acid in a single step process starting from the cheaper base material propane. In the nineteen nineties the Mitsubishi Chemical cooperation published a MoVTeNb-oxide, which could directly oxidise propane to acrylic acid in one step [6], Own preparations of this material yielded a highly crystalline substance. Careful analysis of single crystal electron diffraction patterns revealed that the MoVTeNb-oxide consists of two crystalline phases- a hexagonal so called K-Phase and an orthorhombic I-phase, which is the actual active catalyst phase, as could be shown by preparing the pure phases and testing them separately. 

The equations that describe the magnetic effects and the changes of electron diffraction patterns are got in consequence with the data of X-ray investigation of amorphous alloys and the products of crystallization. 

Initial attempts to prepare Cf metal using metallothermic reduction methods (Section II,A) were less than successful due to the high vapor pressure of Cf metal 28, 46). Reduction of californium oxide with La metal (Section II,B) and collection of the product Cf metal on a fused silica fiber (in the apparatus shown schematically in Fig. 15), were found to give metal with usable X-ray diffraction patterns (5). Later, the same method was used to collect Cf metal both on a fused silica fiber for X-ray diffraction analysis and on an electron microscopy grid for electron diffraction analysis 56). As more Cf became available, preparations via this method were carried out on 0.4-1.0-mg samples of californium oxide (55), using fibers of quartz. Be, or C (suitable for direct X-ray diffraction analysis) to collect the product Cf metal. 

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