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M. W. Evans 《Foundations of Physics Letters》1996,9(4):397-405
The equations of free-space electrodynamics are derived directly from the Riemann curvature tensor and the Bianchi identity of general relativity by contracting on two indices to give a novel antisymmetric Ricci tensor. Within a factore/h, this is the field-strength tensor G of free-space electrodynamics. The Bianchi identity for G describes free-space electrodynamics in a manner analogous to, but more general than, Maxwell's equations for electrodynamics, the critical difference being the existence in general and special relativity of the Evans-Vigier fieldB
(3). 相似文献
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Phenylalanine, tyrosine and dihydroxyphenylalanine (DOPA) were identified unambiguously and quantitatively determined in single ventral thoracic nerve cords from the locust, Schistocerca gregaria, by gas chromatography-negative-ion chemical ionisation mass spectrometry. Deuterium-labelled analogues of each compound were added to a single ventral thoracic nerve cord in hydrochloric acid; the tissue was homogenised and the suspension centrifuged. The remaining hydrochloric acid was eliminated azeotropically by repeated additions of acetonitrile followed by evaporation under a stream of nitrogen and the resultant residue derivatised by reaction with hexafluoroisopropanol and pentafluoropropionic anhydride. Under negative-ion chemical ionisation conditions, the hexafluoroisopropanol-pentafluoropropionyl derivatives produced characteristic ions which were sufficiently abundant to be suitable for selected-ion monitoring. This method is highly specific and gave a limit of detection below the nanogram level. The amounts of phenylalanine, tyrosine and DOPA in a single ventral thoracic nerve cord were, respectively, 194 +/- 81, 347 +/- 88 and 11 +/- 11 ng per tissue. 相似文献
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C. Evans D. Weir J. C. Scaiano A. Mac Eachern J. T. Arnason P. Morand B. Hollebone L. C. Leitch B. J. R. Philogegne 《Photochemistry and photobiology》1986,44(4):441-451
The photochemistry of α-terthienyl (αT) and its mono- and dodo derivatives has been examined using nanosecond laser Hash photolysis techniques. The triplet states of these intermediates have been characterized, and show strong triplet-triplet absorptions with maxima in the 450 to 490 nm region. The triplet lifetimes are normally reduced by efficient triplet-triplet annihilation and self-quenching both of which approach diffusion control. Triplet lifetimes in methanol obtained by extrapolation to zero laser dose and zero concentration are 30, 12.5 and 9.4 μs for αT and its mono- and dodo derivatives, respectively; the effect of iodo substitution on the lifetimes is attributed to heavy atom effects. The triplet states are efficiently quenched by oxygen and the electron acceptor methyl viologen, while amines tire very poor triplet quenchers. The iodo derivatives are photolabile. undergoing C-I bond cleavage from the singlet state, a process that was studied in benzene solvent, where the complex between iodine atoms and benzene can be readily characterized. Modification of αT by replacement of the central thiophene ring by an aromatic ring (i.e. DTB) causes drastic changes in the triplet and singlet state kinetic and spectroscopic characteristics. 相似文献
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Simple yet accurate expressions for the electrical double-layer interaction force and energy between the particles that hold for a wide range of surface potential is required in the modeling, simulation, and optimization of many processes employed in industry. In this paper, simple approximate expressions for the interaction are obtained based on the asymptotic results and the numerical solution to the Poisson-Boltzmann equation for identical parallel plates with constant surface potential up to 180/z(i) mV at 25 degrees C, and the Derjaguin approximation. Within the moderate surface potential range, the semianalytical expressions agree well with the exact numerical results and are convenient to use for the purpose of process modeling and simulation. Copyright 2000 Academic Press. 相似文献
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The differences between the far-infrared absorption of liquid (+)3-methylcyclohexanone and the racemic mixture are interpreted as supporting evidence for the direct observation of rotation-translation coupling. 相似文献
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Wet oxidation of BPL porous carbon by H2O2 and HNO3 changes the pore structure and also increases the concentration of surface oxides. KOH uptake is increased by oxidation and is seen to be dependent on KOH concentration and to a lesser extent on inert electrolyte concentration. Enthalpy of immersion measurements have allowed the estimation of the enthalpy of hydration of the surface oxides and the enthalpy of neutralization of the easily accessible acid oxides. 相似文献