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91.
92.
We explain how the field of logarithmic‐exponential series constructed in 20 and 21 embeds as an exponential field in any field of exponential‐logarithmic series constructed in 9 , 6 , and 13 . On the other hand, we explain why no field of exponential‐logarithmic series embeds in the field of logarithmic‐exponential series. This clarifies why the two constructions are intrinsically different, in the sense that they produce non‐isomorphic models of Th$(mathbb {R}_{mbox{an, exp}})$; the elementary theory of the ordered field of real numbers, with the exponential function and restricted analytic functions. 相似文献
93.
Alharbi F. F. Aman Salma Ahmad Naseeb Ejaz Syeda Rabia Khosa Rabia Yasmin Abid Abdul Ghafoor Manzoor Sumaira Al-Buriahi M. S. Alrowaili Z. A. Farid Hafiz Muhammad Tahir 《Journal of Solid State Electrochemistry》2022,26(5):1251-1258
Journal of Solid State Electrochemistry - Scientists are increasingly interested in improving electroactive technologies for supercapacitor applications, since energy storage devices have improved... 相似文献
94.
Faiçal Abdmouleh Salma Charfi Aref Jeribi 《Journal of Mathematical Analysis and Applications》2012,386(1):83-90
In this paper, we consider the sum and the product of two operators acting on a Banach space and we present some new and quite general conditions to investigate their Wolf, Schechter and Browder essential spectra. 相似文献
95.
Numerical calculations have been done of the viscosity of the soft-sphere liquid, using a new molecular dynamics technique. It is based on a formulation of hydrodynamics which is discrete in space and time, and exactly renormalizable. The present data turn out to be sufficient to estimate the viscosity, but determination of the full equations of motion (and therefore renormalization) requires further calculations using a smaller discrete time interval; these are presently under way. The present results indicate that this method is more than 100 times more efficient than previous (Green-Kubo or nonequilibrium molecular dynamics) methods. This suggests that the discrete formulation is the most natural way to approach hydrodynamics. 相似文献
96.
A dead-time correction system, based on CAMAC-modules is developed for the -ray spectrometry of short-lived radionuclides. The linearity of the method is realized up to about 104 cps. 相似文献
97.
I. Salma L. Almási É. Zemplén-Papp 《Journal of Radioanalytical and Nuclear Chemistry》1990,140(2):263-270
A CAMAC system was installed for pulse height analysis and correction of counting losses due to the dead-time of a multichannel analyzer and the pulse pile-up. A computer program was developed to control the whole system, and to collect and store data in both conventional and cyclic measurement modes. 相似文献
98.
A number of new and interesting 2-amino-4-(N-substituted)imino-4,5-dihydrothiazoles were synthesized by reacting thiourea (or thiourea hydrochloride) with N-alkyl- or N,N-dialkyl-N′-p-toluenesulfonyl-α-chloroacetamidines, where the N,N-alkyl groups were ethyl, cyclohexyl, benzyl, β-phenethyl, (3,5-dimethyl-1-adamantyl)-methyl, as well as N,N-dimethyl- and N,N-pentamethylene. Reactions of N-alkyl-N-p-toluenesulfonyl-2-chloroacetamidines (substituents being N-ethyl, N-benzyl and N,N-dimethyl) with thiourea hydrochloride in hot 2-propanol furnished 2-amino-4-(p-toluenesulfonyl)imino-4,5-dihydrothiazole (in 51, 60 and 65% yields, respectively) and the corresponding amine hydrochloride. In hot acetone or butanone, the reactions of these N-sulfonyl-2-chloroacetamidines with excess thiourea provided 2-amino-4-N-(alkyl or N,N-dialkyl)imminium-4,5-dihydrothiazole chlorides in 25–80% yield. The by-product from these reactions was p-toluenesulfonamide. The structures of the products were established by chemical transformations and spectral methods (nmr and mass spectra). 相似文献
99.
An air pollution study was conducted at two urban residential sites in Budapest from 9 April to 17 May 1996. Size-fractionated aerosol samples were simultaneously collected on a daily basis, and meteorological conditions were recorded at both sampling sites. Stacked filter units (SFUs) with an upper size inlet cutoff were used as sampling devices separating the urban aerosol into coarse [about 2- to 10-μm equivalent aerodynamic diameter (EAD)] and fine (<2 μm EAD) size fractions. In addition, atmospheric concentrations of some criteria pollutants, i.e., NO, NO2, SO2, CO, and total mass of the suspended particulate matter (TSP) were measured every half-hour at one of the sampling sites with commercial equipment. The SFU filters were weighed and analyzed by a light reflectance technique, particle-induced X-ray emission analysis, and instrumental neutron activation analysis. Atmospheric concentrations for 31 aerosol species have been obtained so far. The analytical results were used to characterize the levels and the multielemental composition of the urban aerosol at both sampling sites and for both size fractions, to investigate the atmospheric concentrations and diurnal variation of the criteria pollutants, and to compare the time trends of aerosols and trace gases. The present paper reports on the status of the air pollution study and gives a discussion of the results. 相似文献
100.
A novel sequential injection (SI) method was developed for the determination of penicillamine (PA) and ephedrine (EP) based on the reaction of these drugs with tris(bipyridyl)ruthenium(II) (Ru(bpy)32+) and peroxydisulfate (S2O82−) in the presence of light. Derivatization of PA and EP with aldehydes has resulted in a significant enhancement of the chemiluminescence emission signal by at least 25 times for PA and 12 times for EP, leading to better sensitivities and lower detection limits for both drugs. The instrumental setup utilized a syringe pump and a multiposition valve to aspirate the reagents, (Ru(bpy)32+ and S2O82−), and a peristaltic pump to propel the sample. The experimental conditions affecting the derivatization reaction and the chemiluminescence reaction were systematically optimized using the univariate approach. Under the optimum conditions linear calibration curves between 0.2–24 μg mL−1 for PA and 0.2–20 μg mL−1 for EP were obtained. The detection limits were 0.1 μg mL−1 for PA and 0.03 μg mL−1 for EP. The procedure was applied to the analysis of PA and EP in pharmaceutical products and was found to be free from interferences from concomitants usually present in these preparations. 相似文献