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41.
M. E. Niyazymbetov B. Kostizella I. Keitel K. H. Schwartz 《Russian Chemical Bulletin》1991,40(1):182-186
The cathodic electrolysis of aliphatic alcohols and alkylphosphonates in acetonitrile with 0.5 N Et4NClO4 as the base electrolyte leads to mono- and ditransesterified phosphonates. The yield and ratio of these products is a function of the nature of the starting reagents and amount of current passed.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 1, pp. 200–204, January, 1991. 相似文献
42.
Summary A method is proposed for calculating surface selfdiffusion coefficients in sparingly soluble monolayers at fluid interfaces based on radiotracer measurements and allowing for counter geometry. On this basis an analysis of experimental results is possible without having to allow for processes competing with surface self-diffusion. Monolayers of various long-chainn-alcohols andn-alkane-carboxylic acids were studied in the area range between 0.23 nm2/molecule and 2.0 nm2/molecule. Surface self-diffusion coefficientsD
s
were determinded only up to areas of 0.75 nm2/molecule since, in case of greater areas, the analysis of surface concentration becomes inexact due to the increasing influence of density convection. For the systems studied,D
s
values lie in the order of 10–5 cm2/s. In all compounds studied, the values ofD
s
increase with area per molecule. In addition, dependence on the type of hydrophilic group and alkyl-chain length of monolayer molecules was proved. The results are discussed by means of various model concepts.
With 8 figures and 1 table 相似文献
Zusammenfassung Ein Verfahren zur Berechnung der Oberflächenselbstdiffusionskoeffizienten in schwerlöslichere Monoschichten an fluiden Phasengrenzen auf der Grundlage von Radiotracermessungen und unter Berücksichtigung der Zählrohrgeometrie wird vorgeschlagen. Auf dieser Basis ist eine Auswertung der Experimentalergebnisse möglich, ohne daß zur Oberflächenselbstdiffusion in Konkurrenz stehende Transportvorgänge berücksichtigt werden müssen. Untersucht wurden Monoschichten verschiedener längerkettigern-Alkanole undn-Alkancarbonsäuren im Flächenbereich zwischen 0,23 nm2/Molekül und 2 nm2/Molekül. OberflächenselbstdiffusionskoeffizientenD s wurden nur bis zu Flächenwerten von 0,75 nm2/Molekül bestimmt, weil bei höheren Flächen die Auswertung der Oberflächenkonzentrationsänderungen wegen des zunehmenden Einflusses von Dichtekonvektion ungenau wird. DieD s -Werte liegen für die untersuchten Systeme in der Größenordnung 10–5 cm2/s. Bei allen untersuchten Verbindungen nehmen die Werte von Ds mit steigender Fläche pro Molekül zu. Außerdem wurde die Abhängigkeit von der Art der hydrophilen Gruppe und der Alkylkettenlänge der Monoschichtmoleküle nachgewiesen. Die Ergebnisse wurden anhand verschiedener Modellvorstellungen diskutiert.
With 8 figures and 1 table 相似文献
43.
Daniel Raucher Moshe Levy 《Journal of polymer science. Part A, Polymer chemistry》1975,13(6):1339-1346
The photopolymerization of vinyl fluoride, in the presence of peroxide, was studied in dimethyl sulfoxide (DMSO) solution and in bulk. It was found that high rates of reaction could be obtained in spite of the fact that the polymer precipitates at an early stage. By continuous supply of monomer the precipitated polymer was converted into a transparent bulk polymer. 相似文献
44.
The following Theorem is proved:Let K be a finitely generated field over its prime field. Then, for almost all e-tuples (σ)=(σ 1, …,σ e)of elements of the abstract Galois group G(K)of K we have:
- If e=1,then E tor(K(σ))is infinite. Morover, there exist infinitely many primes l such that E(K(σ))contains points of order l.
- If e≧2,then E tor(K(σ))is finite.
- If e≧1,then for every prime l, the group E(K(σ))contains only finitely many points of an l-power order.
45.
Ricardo Schwartz Schor 《Communications in Mathematical Physics》1978,59(3):213-233
In this work we study thev-dimensional Ising model at low temperatures and establish the existence of an upper gap in the energy-momentum spectrum of the two-point function forv3. Forv=2, it is known that this gap is absent.Supported in part by Conselho Nacional de Pesquisas (CNPq-Brazil), Universidade Federal de Minas Gerais (Brazil) and the National Science Foundation under Grant PHY76-17191 相似文献
46.
Observation of the 35 GHz EPR spectrum of γ-irradiated 10 M NaOH/H2O and 10 M NaOD/D2O glassy ices at 77°K has revealed proton spin flip satellites associated with the trapped elctron EPR line. This suggests that forbidden satellite transitions contribute to the lineshape of the trapped electron line in the 9 GHz spectrum which has commonly been studied. 相似文献
47.
Carbon–hydrogen bond dissociation enthalpies (BDEs) were computed for all haloethenes, C2H4−nXn (n=0–3, X=F, Cl, Br, I), at the B3LYP/6-311+G(3df,2p) level using isodesmic reactions. It was found that C–H bond strengths in the monohaloethenes varied substantially, by as much as 18 kJ mol−1, dependent upon the bond's stereochemical position relative to the halogen. BDEs in the dihaloethanes varied in the order CX2CH–H>(E)-CHXCX–H>(Z)-CHXCX–H. Trends in the computed bond enthalpies were discussed and explained on the basis of relative steric repulsions and hyperconjugative delocalization interactions, as determined from Natural Bond Orbital analysis. 相似文献
48.
P. M. Henrichs J. M. Hewitt L. J. Schwartz D. B. Bailey 《Journal of polymer science. Part A, Polymer chemistry》1982,20(3):775-782
Spin-lattice relaxation times and nuclear Overhauser enhancements (NOE) for 13C nuclei in copolymers of acrylonitrile and vinylidene chloride were measured at 20.1 and 67.9 MHz. In the ? CCl2? region of the spectrum T1 and NOE values of the various resonances are equal within experimental error and are invariant to changes in composition. The T1 and NOE values of the ? CCl2? region, however, are not equal to those of the ? CH? or ? CN region. As a result compositions cannot be calculated by direct comparison of the areas in the ? CCl2? region and either the ? CH? or the ? CN region. Discrepancies can be corrected for the ? CH? resonances by multiplication of the area by an empirical constant. A similar constant for the ? CN region is composition-dependent at 20.1 and 67.9 MHz. A chemical shift anisotropy mechanism is postulated as important for relaxation of the ? CN resonances. The overall influence of variable T1 and NOE values on quantitative determination of polymer composition is considered. 相似文献
49.
50.
Recent developments in the field of reactive compatibilization of polymer blends prepared by melt processing focus on the addition of low molecular weight compounds. This work deals with in situ compatibilization through the formation of graft or crosslinked copolymers at the interface. Mixtures of semicrystalline hydrocarbon polymers have been subjected to free radical reactivity, in a co-rotating twin screw extruder (ZSK 30) in a single step. The particular system, high density polyethylene and polyamide 6, was blended in the presence of a peroxide and a reactive bifunctional monomer, maleic anhydride. Because of a combined effect, the reaction appears to occur mainly at the interface, where the resulting grafted copolymer acts as an anchor for the final stabilization of the biphasic system. Different analytical techniques, such as differential scanning calorimetry, scanning electron microscopy and tensile testing, helped in characterizing the resulting blends and confirmed the high level of interfacial grafting and the expected improvement in mechanical properties. 相似文献