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951.
The thermal decomposition of some M
2
I
HPO3 (M-Li, Na, K) phosphites under nitrogen atmosphere was investigated. A stepwise mechanism of thermal decomposition has been proposed.
Zusammenfassung Es wurde die thermische Zersetzung von Phosphiten M 2 I HPO3 (M-Li, Na, K) in Stickstoffatmosphere untersucht. Die Schritte des Mechanismus der thermischen Zersetzung wurden vorgeschlagen.相似文献
952.
J. Magoński 《Journal of solution chemistry》1990,19(6):597-607
The significant role of the proton exchange and homoconjugation (formation of AHA– and A1HA
1
–
complexes) equilibria in protonic hetero systems (HA+A
1
–
) has been shown from analysis of published data and from my own simple experiments. It is concluded that there is a need to reconsider some basic hydrogen bond problems. One of these problems-the existence of heteroconjugates in polar solvents — has been verified and illustrated with suitable experimental evidence (IR and UV-VIS spectra). The most accepted experimental evidence for the double minimum potential in the hydrogen bridge has been questioned as being in disagreement with the equilibrium law. A simple relation between the heteroconjugation constant, the parent homoconjugation constants and the proton exchange constant is also postulated. This relation fulfills important theoretical requirements, however, it is not applicable in extreme cases.To the memory of Bogdan Przybyszewski. 相似文献
953.
D. Rosmann K. -W. Klinkhammer A. Schmidt 《Monatshefte für Chemie / Chemical Monthly》1996,127(5):461-468
Zusammenfassung Arsen-tris(2,2-dimethylpropionat) (1) kristallisiert monoklin in der Raumgruppe P21/n mita=926.2,b=2158.6,c=983.7 pm, =94.92° undZ=4. As hat gegenüber O die Koordinationszahl 3+3. Antimontripropionat (2) kristallisiert monoklin in der Raumgruppe P21/c mita=930.2,b=863.0,c=1575.2 pm, =90.27 undZ=4. Die Moleküle sind intermolekular zu Ketten verknüpft, wodurch Sb die Koordinationszahl 3+3 (+3) erreicht.
Structure of arsen(III) and antimony(III) carboxylates
Summary Arsen-tris(2,2-dimethylpropionate) (1) crystallizes monoclinic in the space group P21/n witha=926.2,b=2158.6,c=983.7 pm, =94.92°, andZ=4. As has a coordination number of 3+3. Antimony tripropionate (2) crystallizes monoclinic in the space group P21/c witha=930.2,b=863.0,c=1575.2 pm, =90.27, andZ=4. The molecules are bridged to chains; therefore, Sb reaches the coordination number 3+3 (+3).相似文献
954.
D. Duracher F. Sauzedde A. Elaissari A. Perrin C. Pichot 《Colloid and polymer science》1998,276(3):219-231
Cationic hydrophilic copolymer latexes were synthesized at 70 °C either by batch or two-step emulsifier-free emulsion poly-merization
of styrene (St), N-iso-propylacrylamide (NIPAM), and aminoethylmethacrylate hydro-chloride (AEM) using 2,2′-azobis (2-amidinopropane) dihydrochloride
as initiator. At first, batch polymerization kinetics were followed by gas chromatography (GC), revealing that NIPAM rapidly
homopolymerized, before the polymerization of styrene had started. Particle size analysis by quasi-elastic light scattering
(QELS) and transmission electron microscopy (TEM) showed that monodispersed particles were obtained with the formation of
a poly[NIPAM] rich shell. Adding a small amount of the cationic monomer caused a strong decrease of the particle size without
affecting the size monodispersity. When a shot process was used, a narrow particle size distribution was maintained, provided
that the monomer addition was performed at a relatively high conversion of the first batch step. The poly[NIPAM] rich shell
layer was larger with the shot process, but increasing the amino-containing monomer in the recipe resulted in a dramatic decrease
of the thickness. Combination of transmission, scanning and atomic force microscopy techniques showed that these hydrophilic
particles exhibited odd-shaped structures, the unevenness being dependent upon the performed process. Kinetic data and particle
morphology information were inferred for discussion of the polymerization mechanism of this system.
Received: 21 August 1997 Accepted: 22 October 1997 相似文献
955.
H. Balard M. Sidqi E. Papirer J. B. Donnet A. Tuel H. Hommel A. P. Legrand 《Chromatographia》1988,25(8):712-716
Summary The surface properties of silicas modified with – diols having between 4 and 16 carbon atoms were investigated by inverse gas chromatography. It is shown, that the value of the dispersive component of the surface energy does not change monotonously: a minimum value is recorded when the surface is covered by a monolayer of methylene groups. Further, when measuring the adsorption enthalpies of polar probes, an alternation of their H values is observed: grafts having an odd number of carbon atoms systematically show higher H values than the others. A trans-trans configuration of the grafted chains which allows optimum interactions is proposed, suggesting a preferential diesterification reaction of both terminal hydroxyl groups of odd diols. 相似文献
956.
Heat transfer from a plasma flow to a metallic or nonmetallic spherical particle is studied in this paper for the extreme case of free-molecule flow regime. Analytical expressions are derived for the heat flux due to, respectively, atoms, ions, and electrons and for the floating potential on the sphere exposed to a two-temperature plasma flow. It has been shown that the local or average heat flux density over the whole sphere is independent of the sphere radius and approximately in direct proportion to the gas pressure. The presence of a macroscopic relative velocity between the plasma and the sphere causes substantially nonuniform distributions of the local heat flux and enhances the total heat flux to the sphere. The heat flux is also enhanced by the gas ionization. Appreciable difference between metallic and nonmetallic spheres is found in the distributions along the oncoming flow direction of the floating potential and of the local heat flux densities due to ions and electrons. The total heat flux to the whole sphere is, however, almost the same for these different spheres. For a fixed value of the electron temperature, the heat flux decreases with increasing temperature ratio Te/Th. 相似文献
957.
Summary The interaction of some benzene and naphthalene derivatives with sodium dodecyl sulphate, hexadecyltrimethylmmonium bromide and polyoxyethylene [23] dodecanol micelles has been evaluated by high operformance liquid chromatography using micellar mobile phases. The micelle-solute association constants have been obtained for the compounds investigated. Good correlation between free energy of transfer for water-micelles and for octanol-water has been observed. 相似文献
958.
U. K. Chakrabarti S. J. Pearton W. S. Hobson C. R. Abernathy 《Plasma Chemistry and Plasma Processing》1993,13(2):333-350
Vinyl iodide (C2H3I) microwave discharges with additions of H2 and Ar are found to provide faster etch rates than conventional CH4/H2/Ar discharges for InP, InGaAs, GaAs, and AlGaAs. This is a result of the relatively high volatilities of indium, gallium, and aluminum iodide species. The etched features are smooth and anisotropic over a wide range of do self-biases (–150 to –350 V), process pressures (1–20mTorr), and microwave powers (150–500 W). The polymer that forms on the mask during the plasma exposure can be readily removed in O2 discharges. Electron spectroscopy for chemical analysis (ESCA) showed that the etched surfaces are slightly deficient in the group V elements under most conditions, but changes to the optical properties of the semiconductors are minimal. No defects are visible by transmission electron microscopy (TEM) in GaAs or InP samples etched at dc biases –250 V. 相似文献
959.
A. N. Ageev A. A. Aratskova L. D. Belyakova T. N. Gvozdovich A. V. Kiselev Ya. I. Yashin J. Kàlal F. Švec 《Chromatographia》1983,17(10):545-548
Summary The retention of benzene derivatives with nonpolar and polar substituents on a porous methacrylate copolymer containing epoxy groups using both nonpolar and polar eluents was investigated. When n-hexane is used as the eluent, the retention of n-alkylbenzenes and polymethylbenzenes is weaker than that of benzene. In the case of benzene derivatives containing polar functional groups their capacity ratios (k) on this porous polymer increases approximately linearly with the increase of the adsorbate molecules dipole moment. The retention characteristics of the methacrylate copolymer were compared with that of a styrene-divinylbenzene copolymer and silica gels with a hydroxylated surface and with a surface modified by chemically bonded alkylsilyl groups. 相似文献
960.