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181.
The adsorption of CO2 on a raw activated carbon A and three modified activated carbon samples B, C, and D at temperatures ranging from 303 to 333 K and the thermodynamics of adsorption have been investigated using a vacuum adsorption apparatus in order to obtain more information about the effect of CO2 on removal of organic sulfur-containing compounds in industrial gases. The active ingredients impregnated in the carbon samples show significant influence on the adsorption for CO2 and its volumes adsorbed on modified carbon samples B, C, and D are all larger than that on the raw carbon sample A. On the other hand, the physical parameters such as surface area, pore volume, and micropore volume of carbon samples show no influence on the adsorbed amount of CO2. The Dubinin-Radushkevich (D-R) equation was the best model for fitting the adsorption data on carbon samples A and B, while the Preundlich equation was the best fit for the adsorption on carbon samples C and D. The isosteric heats of adsorption on carbon samples A, B, C, and D derived from the adsorption isotherms using the Clapeyron equation decreased slightly increasing surface loading. The heat of adsorption lay between 10.5 and 28.4 kJ/mol, with the carbon sample D having the highest value at all surface coverages that were studied. The observed entropy change associated with the adsorption for the carbon samples A, B, and C (above the surface coverage of 7 ml/g) was lower than the theoretical value for mobile adsorption. However, it was higher than the theoretical value for mobile adsorption but lower than the theoretical value for localized adsorption for carbon sample D. 相似文献
182.
The molar heat capacity of the azeotropic mixture composed of ethanol and toluene was measured by a high precision adiabatic calorimeter from 80 to 320 K. The glass transition and phase transitions of the azeotropic mixture were determined based on the heat capacity measurements. A glass transition at 103.350 K was found. A solid-solid phase transition at 127.282 K, two solid-liquid phase transitions at 153.612 and 160.584 K were observed, which correspond to the transition of metastable crystal to stable crystal of ethanol and the melting of ethanol and toluene, respectively. The thermodynamic functions and the excess ones of the mixture relative to the standard temperature 298.15 K were derived based on the relationships of the thermodynamic functions and the function of the measured heat capacity with respect to temperature. 相似文献
183.
C. Jolicoeur B. Riedl D. Desrochers L. L. Lemelin R. Zamojska O. Enea 《Journal of solution chemistry》1986,15(2):109-128
The limiting partial molar volumes V
o
and heat capacities C
p
o
of 20 amino acids have been determined in water and in 8 molar urea at 25.0°C using flow calorimetry and flow densimetry. The side chain contributions to V
o
and C
p
o
were obtained as the difference between the properties of the various amino acids and those of glycine, both in water and in 8M urea. The solvent accessible surface area of the amino acid residues were obtained using a method developed by Hermann, and the total surface areas were separated into their hydrophobic A
Hb
and hydrophilic components. In water, C
p
o
values for the various residues C
p
o
(R) were found well correlated with A
Hb
, though much less so in the urea solution. Hence, C
p
o
(R) values, in water yield a good estimate of side chain hydrophobicity, but the (waterurea) transfer heat capacities appear strongly affected by specific solvation effects in the urea solution.Presented at the sixth Italian meeting on Calorimetry and Thermal Analysis (AICAT) held in Naples, December 4–7, 1984. 相似文献
184.
Heat capacities C
p
and volumes V have been obtained at 25°C for the transfer of cholesteryl oleyl carbonate (ChOC) from a reference solvent, the highly-branched alkane 2,2,4,4,6,8,8-heptamethylnonane into various solvents. These include normal, branched, and cyclic alkanes as well as the pure cholesteric ChOC. V and most C
p
are associated with the change of environmental free volume during the transfer process and are predicted by the Prigogine-Flory theory. However, for n-alkane solvents with more than twelve carbons, C
p
is large, positive, and unattributable to free volume changes. It is consistent with a restriction of alkane segmental motion by the ChOC. The same mechanism has been proposed to explain an antiplasticization effect of ChOC on transitions in polymers. 相似文献
185.
The adsorption equilibrium of water on microporous adsorbents (zeolites of NaA-, NaY- and NaX-type as well as their ion exchanged
forms) and on mesoporous adsorbents (different silica gels and composite material i.e. silica gel + salt hydrate) has been
studied experimentally and theoretically. Using the Dubinin theory of pore filling the characteristic curves of the adsorption
systems and other relevant dependences such as isotherms, isobars, isosteres and the curve of the differential heat of adsorption
were calculated. For all systems investigated the adsorption were calculated. Aads and the desorption potential Ades of the closed heat storage system were estimated. These values define the working range of the adsorption/desorption cycle
and allow to calculate the specific heat storage density Δ hsp. On the basis of Δ hsp the different adsorbents were compared in order to select the optimal porous storage material for a given application.
The presented experimental and theoretical investigations show that the adsorption systems water-zeolite and water-composites
are promising working pairs for thermochemical heat storage processes for hot tap water supply and space heating of single
family dwellings. The advantage of the water-composite system is the low desorption temperature (solar energy) the main shortcoming
the low temperature lift. The advantage of the water zeolite system is the high temperature lift, the shortcoming are the
relative high desorption temperatures. 相似文献
186.
A simple equation has been derived relating the temperature dependence of activity functions with excess enthalpies and excess heat capacities. Using experimentally determined parameters at 298.15°K, it is possible to predict osmotic coefficients and mean activity coefficients of alkali halides in water up to 1 m from 273°K to about 350°K. In general, the predicted functions agree with the measured values within the uncertainty of the activity data. An equation is also given for the pressure dependence of the excess free energies, but it was not possible to check the limitation of this equation due to lack of activity data at various pressures.To whom correspondence should be addressed. 相似文献
187.
188.
Rainer P. H. Garten 《中国化学会会志》1994,41(3):259-274
Selected prominent problems in the analysis of advanced ceramic materials are surveyed. The importance of reliability of results is discussed in the field of elemental trace- and microanalysis in view of its interaction with economy, power of detection, local resolution and speciation selectivity. Particular problems in the analysis of major constituents, trace components and microlocal distributions are based on the striking propertics of ceramics; they are exemplified. Analytical assistance must start from the beginning of the production processing, in the preparation of the powdered base materials. Determination of the stoichiometry requires high accuracy and differentiation of chemical species in bulk and surface analysis of ceramic base powders. Element trace determination by direct instrumental methods requires standard reference materials for calibration; these are currently inavailable in a sufficient variety. For optimum reliability and power of detection, element traces must be prepared in isolated form in a small excitation volume for analysis. A review on the state-of-the-art of wet-chemical combined procedures is presented. Decomposition position procedures are emphasized, due to their risk of contributing severe systematic error. Combustion in elementary fluorine is presented for decomposition of refractory materials. The performance of some direct procedures is discussed. Very efficient methods are available for element trace determinations in ceramic materials, offering high detection power. Several approaches for high-resolution local microanalysis in non-conductive ceramic materials are identified as the most promising development in the analysis of sintered compact ceramic products and devices. 相似文献
189.
Zhengjie Pi Joseph P. Kennedy James W. Summers 《Journal of polymer science. Part A, Polymer chemistry》2002,40(21):3644-3651
The tertiary chlorine (Clt) content of vinyl chloride/2‐chloropropene copolymers [P(VC‐co‐2CP)] was determined by NMR spectroscopy. Copolymers containing 6.8–47.0 Clt's per P(VC‐co‐2CP) chain were used to initiate the cationic grafting of α‐methylstyrene, norbornadiene, indene, and norbornene with Et2AlCl under various conditions. Grafting was demonstrated by selective solvent extraction, and the effect of the experimental conditions on the grafting efficiency was examined. Select rheological and thermal characteristics of P(VC‐co‐2CP) grafts, including the glass‐transition temperature, heat deflection temperature, and discoloration upon heating, were studied. P(VC‐co‐2CP) carrying 7–11 poly(α‐methylstyrene) or polynorbornadiene branches per chain raised the glass‐transition temperature to, or above, that of a blend control. P(VC‐co‐2CP)s fitted with polyindene or polynorbornene branches were less effective in raising the mechanical properties. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 3644–3651, 2002 相似文献
190.
Z. L. Zhang M. H. Zhong J. Liu F. M. Liu Z. Z. Wang F. P. Zhong F. Wu 《Journal of Thermal Analysis and Calorimetry》1999,58(2):421-433
In this work some calorimetric measurements were also carried out on the electrorefining silver by using different current densities with a Calvet type microcalorimeter at room temperature. The ratio (R) of the measured heat (
m) to the input electric energy (
in) and the excess heat (
ex), i.e., difference between
m and
in during the electrorefining process, were discussed in terms of general thermodynamics. It was found that the R and
ex for silver were related with the current density or cell voltage employed in the experiment. The results obtained here also indicate that the heat generation under different conditions, such as different currents or voltages may be caused partially by the irreversibility of the process or by some unknown processes.This revised version was published online in November 2005 with corrections to the Cover Date. 相似文献