Linking numbers appear in local quantum field theory in the presence of tensor fields, which are closed two-forms on Minkowski space. Given any pair of such fields, it is shown that the commutator of the corresponding intrinsic (gauge-invariant) vector potentials, integrated about spacelike separated, spatial loops, are elements of the center of the algebra of all local fields. Moreover, these commutators are proportional to the linking numbers of the underlying loops. If the commutators are different from zero, the underlying two-forms are not exact (i.e. there do not exist local vector potentials for them). The theory then necessarily contains massless particles. A prominent example of this kind, due to J.E. Roberts, is given by the free electromagnetic field and its Hodge dual. Further examples with more complex mass spectrum are presented in this article.
We consider some reaction–diffusion equations perturbed by white noise and prove Schauder estimates for the elliptic problem
associated with the generator of the corresponding transition semigroup, defined in the Banach space of continuous functions.
This requires the proof of some new interpolation result. 相似文献
We consider local minimizers of elliptic variational integrals with integrand f of nearly linear growth. In the scalar case N= 1 a side condition of the type u≥Φ may be incorporated, for N > 1 u is an unconstrained minimizer and f is required just to depend on the modulus of Du. We show in both cases that u has H?lder continuous first derivatives in the interior of the domain Ω. 相似文献
The rates of the mononuclear heterocyclic rearrangement of the phenylhydrazone of 3-benzoyl-5-phenyl-1,2,4-oxadiazole (1) into 2,5-diphenyl-4-benzoylamino-1,2,3-triazole (II) have heen measured in dioxane/water (50:50, v:v) in the range of pS+ 3.8–12.2 at various temperatures and the activation parameters determined. On the basis of the results obtained, we present evidence for the occurrence of two different types of reaction: the first, base-catalyzed; the second, pS+ -independent. In the base-catalyzed range the catalysis is of the general type. 相似文献
Chlorodifluoroacetyl azide, ClF(2)CC(O)N(3), was prepared and characterized by IR (gas, Ar matrix), Raman (liquid), UV-vis (gas), and (19)F, (13)C NMR spectroscopy. The vibrational spectra were analyzed in terms of a single conformer, gauche-syn, where the Cl-C and the N(α)═N(β) bonds are gauche and syn to the C═O bond, respectively. The photo and thermal decomposition reactions of the azide were studied with the aid of matrix isolation. In both cases, a new isocyanate species ClF(2)CNCO was produced and characterized by matrix IR spectroscopy. The conformational properties and the Curtius rearrangement pathways of this new carbonyl azide were theoretically explored, which suggest the preference of a concerted over stepwise decomposition for the global minimum gauche-syn conformer. 相似文献
High resolution infrared spectra (0.001 cm−1 FWHM) have been measured for mixtures of 1-chloro-1,1-difluoroethane in Ne, expanded in a supersonic planar jet. The ν6 fundamental, infrared active with a dominant parallel transition moment, exhibits a remarkable splitting of about 0.035 cm−1 for both 35Cl and 37Cl isotopomers. Several mechanisms of interaction of ν6 with states with high torsional excitation are critically examined to explain the observed effect. It is concluded that the observed torsional splitting patterns can be explained in terms of a torsional Coriolis interaction between ν6 and a highly excited torsional mode, 6ν18. A full numerical analysis, performed including a torsional Coriolis term in the Hamiltonian, shows that the interaction mechanism requires a torsional barrier height of about 1270 cm−1. 相似文献
New photosensitive materials can be obtained by electrochemical oxidation of thiocyanate and selenocyanate salts. Using (K,Na)SCN eutectic melt, the formation of an electrodic deposit, with photoelectrochemical properties, has already been reported by us. To improve the photoelectrochemical characteristics of the deposit, futher investigations were carried out in the following sistems: selenocyanate ammoniate, KSCH-Acetamide eutectic mixture and KSCN ethylene carbonate solution:. Attempts to obtain a massive deposit in the ammoniate solution were unsuccessful due to ammonia oxidation. Measurements performed on the other KSCN systems show that temperature is a parameter of remarkable importance. In fact, lowering the temperature one obtains a decrease on formation of parathiocyanogen on behalf of the polytrithiocyanogen, the species that gives rise to the photoeffect. 相似文献