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排序方式: 共有494条查询结果,搜索用时 15 毫秒
1.
A protocol to correct for intra‐ and interspecific variation in tail hair growth to align isotope signatures of segmentally cut tail hair to a common time line
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2.
Reactions of the hydrated electron, H atoms, 2-propanol, and methanol radicals with the TiO2 nano-particles have been studied either directly or by competition kinetics. The radicals were produced by radiolysis of 2-propanol, t-butanol, or methanol aqueous solutions in acid pH's. The reactions involve electron injection to the conduction band. As expected, the t-butanol radical is inert towards TiO2 under our conditions, while the other reducing radicals react with TiO2. The reactivity decreases in the order: eaq−>H>CH3COHCH3>CH2OH. Two TiO2 nanocrystallite sizes, with average diameters of 1.0 and 4.7 nm were compared. For equal concentrations (in terms of TiO2 molecules), the rate of electron injection shows relatively little dependency on particle size. The rates of interfacial electron transfer and transfer coefficient are also reported. 相似文献
3.
The temporal characteristics of stimulated Raman scattering (SRS) under 22-ps laser excitation were studied in eight oxide crystals with a T 2 optical-phonon dephasing time variable by up to two orders of magnitude. The measured SRS pulse width was shortened from 13.8 ps for Ba(NO3)2 (T 2 = 26.5 ps) to 4 ps for the LiNbO3 (T 2 = 0.38 ps) crystal. The dependence of SRS pulse width on the dephasing time was analyzed in the framework of the known SRS theory. 相似文献
4.
Picosecond stimulated Raman scattering in crystals 总被引:1,自引:0,他引:1
T. T. Basiev P. G. Zverev A. Ya. Karasik V. V. Osiko A. A. Sobol’ D. S. Chunaev 《Journal of Experimental and Theoretical Physics》2004,99(5):934-941
The comparative values of the peak and integral cross sections of spontaneous Raman scattering and the optical dephasing time of molecular vibrations were determined for several oxide crystals by spontaneous Raman spectroscopy. The spectral, time, and energy parameters of stimulated Raman scattering (SRS) were measured for ten crystals using picosecond YLF: Nd laser pumping with a radiation wavelength of 1047 nm. An analysis of the experimental dependence of the threshold energy of pumping SRS on the integral and peak cross sections of spontaneous Raman scattering showed that the SRS gain increment explicitly depended on the integral cross section and was independent of the peak cross section of spontaneous Raman scattering as the ratio between the pumping pulse width (11 ps) and the time of optical dephasing of molecular vibrations changed from 0.42 to 9.3. The gain coefficients of steady-state stimulated Raman scattering under threshold stimulated Raman scattering conditions were determined for all the crystals studied on the basis of the measured threshold SRS pumping energies, the duration and width of the spectrum of pulses, the nonlinear interaction length, the intensity of pumping, and the theoretical dependences that relate the steady-state and transient SRS gain increments. The steady-state SRS gain coefficients obtained in this work fitted well a linear dependence on the peak cross sections of spontaneous Raman scattering, which substantiated the correctness of our analysis and measurements. 相似文献
5.
Agnes Kurucz 《Algebra Universalis》2002,47(4):409-424
We show that in many cases the decision problems for varieties of cylindric algebras are much harder than those for the corresponding relation algebra reducts. We also give examples of varieties of cylindric and relation algebras which are algorithmically more complicated than the subvarieties of their representable algebras. 相似文献
6.
The reaction of bis(hydroxymethyl)phenylphosphine with isobutyl diphenylborate in the presence of triethylamine leads to the formation of triethylammonium 2,2,5-triphenyl-1,3,2,5-dioxaborataphosphorinane (1). The reaction of compound 1 with electrophilic reagents (O, S, Se, CH2O, RHal) leads to quaternization of the phosphorus atom, giving the corresponding phosphine oxides, sulfides, and selenides and P,B-containing betaines. In the reactions of compound 1 with amines aminomethylphosphines of the diazaphosphorinane and diazadiphosphacyclooctane series are formed. Ammonium 1,3,2,5-dioxaborataphosphorinanes dissociate in solutions and enter into ion exchange with phosphonium iodides, leading to phosphonium 1,3,2,5-dioxaborataphosphorinanes. The latter, in the case of the aminomethylphosphonium cation, undergo intramolecular rearrangement with the formation of P,B-containing betaines and aminomethylphosphines.Deceased.A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan' Scientific Center, Russian Academy of Sciences, 420083 Kazan'. Translated fromIzvestiya Akademii Nauk, Seriya Khimicheskaya, No. 6, pp. 1398–1405, June, 1992. 相似文献
7.
Szantai E Ronai Z Szilagyi A Sasvari-Szekely M Guttman A 《Journal of chromatography. A》2005,1079(1-2):41-49
The investigation of the genetic background and phenotype structures of complex diseases, such as cardiovascular or psychiatric disorders and tumors, is one of the most scrutinized fields of the post genomic era. Besides the multiplex analysis of genetic markers and polymorphisms throughout the whole genome, more and more attention is focused on the interaction between the etiological factors of these traits. Haplotype determination, rather than multiplex genotyping seems to be one of the first building blocks of this endeavor. This review focuses on the importance and theoretical background of haplotyping, and summarizes the recent examples of novel and emerging haplotyping techniques by capillary gel electrophoresis based DNA fragment analysis, a powerful tool for the examination of the inheritance of complex traits. 相似文献
8.
Agnes G. Nagy 《Journal of organometallic chemistry》1985,291(3):335-340
Polarizations, polarization ranges and ratios of polarization ranges for vinylene groups in seven series, namely chalcone derivatives, ferrocene analogues of chalcone, stilbene derivatives, ferrocene analogues of stilbene, and styrene derivatives, were studied. The polarization ranges spanning the intervals between 13C NMR chemical shifts of the derivatives substituted by p-NO2 and p-NMe2 groups are compared in these related compounds. The influence of the side-chain groups in the vinylene moiety and of the sign of the polarization on the substituent-effect are discussed. 相似文献
9.
10.
Tamas Benko Agnes Szanyi Peter Mizsey Zsolt Fonyo 《Central European Journal of Chemistry》2006,4(1):92-110
The sustainable development and consumption need more efficient use of natural resources. As a consequence, the use of industrial
solvents demands their recovery instead of end-of-pipe treatment. It is not always clear, however, which treatment alternative
should be applied. Based on an industrial case study, the environmental and economic evaluation and comparison of the treatment
alternatives of a non-ideal solvent mixture containing azeotropes is investigated for determining the preferable option. For
the recovery of the industrial solvent mixture, two different separation alternatives are evaluated: a less effective alternative
and a novel design based on hybrid separation tools. An end-of-pipe treatment alternative, incineration, is also considered
and the split of the solvent mixtures between recovery and incineration is investigated. The environmental evaluation of the
alternatives is carried out using ‘Eco-indicator 99 life-cycle impact assessment methodology’. Economic investigation is also
accomplished. The economic features clearly favour the total recovery, however, the environmental evaluation detects that
if a recovery process of low efficiency is applied, its environmental burden can be similar or even higher than that of the
incineration. This motivates engineers to design more effective recovery processes and reconsider the evaluation of process
alternatives at environmental decision making. 相似文献