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31.
Robert C. Hopkins 《Journal of Polymer Science.Polymer Physics》1969,7(11):1907-1918
A new apparatus for investigating dynamic strain birefringence in polymer films at frequencies up to 10 Hz and at various degrees of internal sample orientation is described. Samples are elongated at constant low rates while simultaneously being strained sinusoidally. Fast changes in sample retardance are recorded while slow changes are automatically compensated with a servo-controlled Soleil-Babinet compensator. The signal-to-noise ratio of the system is greatly enhanced by incorporating a highly monochromatic laser light source, a synchronous amplifier, and a light beam modulator based on a rotating polarizer. Data obtained from this apparatus can be used to elucidate polymer relaxation mechanisms at various frequencies over a wide range of static strains. 相似文献
32.
The equilibrium segregation in the system W(100) plus two monolayers of total carbon content has been studied in the range 1600 to 2073 K. The energy of segregation is ?56(±2) kcal mole?1. The kinetics of carbon segregation at 1350 and 1420 K were observed. From a semi-empirical treatment an upper limit to the activation energy for volume diffision is deduced to be 59 (±8) kcal mole?1. 相似文献
33.
Daniel E. Haines Vincent M. Miskowski Michael D. Hopkins 《Journal of Cluster Science》2004,15(4):489-502
An analysis of the available electrochemical and electronic-sectroscopic data for quadruply metal–metal bonded complexes reveals that the 1(*) transition energy is an approximately linear function of the difference between the electrode potentials at which they are reduced and oxidized to the bond-order 3. 5 complexes. A theoretical framework for interpreting this correlation is provided by extending to the redox potentials a simple zero-differential-overlap model previously applied to 1(*) transition energies. It is suggested on the basis of this model that the simplicity of the empirical relationship between 1(*) energies and redox potentials is a consequence of the particular one- and two-electron energy terms that characterize these complexes; a linear relationship is not required by theory. 相似文献
34.
Hopkins JM Bowdridge M Robertson KN Cameron TS Jenkins HA Clyburne JA 《The Journal of organic chemistry》2001,66(17):5713-5716
Reactions of the nucleophilic carbene 1,3-dimesityl-imidazol-2-ylidene (1) with diazofluorene, diphenyldiazomethane, and azidotrimethylsilane were examined. Specifically, carbene 1 reacts with diazofluorene and diphenyldiazomethane to give addition products (azines: 3 and 4, respectively). Compounds 3 and 4 were further characterized in the solid-state by single-crystal X-ray crystallographic studies. [3 (a = 9.7936(6) A, b = 10.0529(7) A, c = 16.251(1) A, alpha = 75.765(1) degrees, beta = 79.711(1) degrees, gamma = 64.321(1) degrees, Z = 2, space group P1); 4 (a = 11.681(3) A, b = 11.861(4) A, c = 21.186(3) A, alpha = 90 degrees, beta = 97.05(2) degrees, gamma = 90 degrees, Z = 4, space group P2(1)/n)]. The structural parameters of 3 and 4 are discussed with reference to previously characterized symmetrical and unsymmetrical azines. Structural data suggest that charge separation is possible in 3. 相似文献
35.
The space group of alpha(')-NaV2O5 turns below T(c) = 34 K from Pmmn with all V sites equivalent, into Fmm2 with three independent vanadium sites per layer. This is incompatible with models of charge ordering into V4+ and V5+. Our structure determination indicates that the phase transition consists of a charge ordering with three distinct valence states, formally V4+, V4.5+, and V5+. The singlet formation is not associated with dimerization on the spin ladder, but with the formation of spin clusters. Finally, we ascribe the quadrupling of the c axis to the large polarizability of the V2O5 skeleton. 相似文献
36.
Acoustic performance in ultrasonic transmitters can be improved by means of a suitable electrical driving response and matching/tuning networks. It is important to predict this electrical response, but doing so is not easy because it departs notably from the nominal pattern with the loading probes. In practice, the analysis of HV pulser spikes in NDE applications requires fairly complex models in the transient regime and, in addition, non-linear problems could arise, especially in the case of tuned transmitters. In this paper, the most relevant influences of loading characteristics of NDT ultrasonic probes on the pulser electrical driving responses are evaluated in time and frequency domains. Conventional pulse generators and typical NDE pulsers are considered. Driving responses are analysed across commercial ultrasonic probes and, alternatively, across similar purely electrical loads. Distinct influences on pulser responses from electrical and motional sections of the probes are identified. All these aspects are studied on the basis of experimental and computer results. 相似文献
37.
38.
F. G. Hopkins G. v. Ritter M. Krüger und W. Smidowitsch 《Fresenius' Journal of Analytical Chemistry》1896,35(1):727-728
Ohne Zusammenfassung 相似文献
39.
E. Cohen J. W. Commelin Pfeffer van 't Hoff Ladenburg Adie Tammann Raoult Naccari Ponsot H. N. Morse D. W. Horn J. C. W. Frazer B. S. Hopkins E. J. Hoffmann W. L. Kennon L. F. Lovelace W. W. Holland F. M. Rogers P. B. Dunbar B. Mears B. F. Lovelace Berkeley Hartley Barlow und L. Kahlenberg 《Fresenius' Journal of Analytical Chemistry》1909,48(4-5):273-278
Ohne Zusammenfassung 相似文献
40.
C. G. Hopkins 《Fresenius' Journal of Analytical Chemistry》1899,38(7):461
Ohne Zusammenfassung 相似文献