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81.
A novel alcohol dehydration membrane with a three layer structure has been prepared. The top layer is a thin dense film of chitosan (CS), and the support layer is made of microporous polyacrylonitrile (PAN). Between the dense and microporous layer, there is an intermolecular cross-linking layer. This novel composite membrane has a high separation factor of more than 8000 and a good permeation rate of 0.26 kg/m2 h for the pervaporation of 90 wt% ethanol aqueous solution at 60°C, 0.8 kg/m2 h flux for a n-PrOH/water system and around 1 kg/m2 h flux for an i-PrOH/water system using 80 wt% alcohol concentration at 60°C. The separation factor for both cases is more than 105. The separation performance varies with feed composition, operating temperature and conditions of membrane preparation. The results show that the separation factor and flux of this membrane increase with raising the operating temperature. At the same time, the crosslinking layer improves durability of the composite membrane, and the pervaporation performance can be adjusted by changing the structure of the cross-linking layer. The cross section of the composite membrane has been examined by SEM. 相似文献
82.
Poly(vinyl chloride) (PVC)-based membrane of pentathia-15-crown-5 exhibits good potentiometric response for Hg2+ over a wide concentration range (2.51 × 10−5 to 1.00 × 10−1 mol dm−3) with a slope of 32.1 mV per decade of Hg2+ concentration. The response time of the sensor is as fast as 20 s. The electrode has been used for a period of six weeks and exhibits fairly good discriminating ability towards Hg2+ in comparison to alkali, alkaline and some heavy metal ions. The electrode can be used in the pH range from 2.7 to 5.0. 相似文献
83.
84.
Poly(dimethylsiloxane) (PDMS)-HTiNbO5 nanocomposite membranes with various HTiNbO5 nanofiller content were prepared by melt intercalation. WAXS diffraction measurements and TEM observations have suggested that the HTiNbO5 mineral was exfoliated in the PDMS matrix. The influence of the filler in the membrane was evaluated by water diffusion, gas permeation (CO2, N2, O2, ethane and ethylene), toluene pervaporation and by CO2 sorption measurements.A filler content of only 2 wt.% in PDMS-HTiNbO5 nanocomposite membranes slows down the water diffusion significantly, and a filler content of 5 wt.% reduces also the permeability of the films for toluene. The addition of a filler content up to 10 wt.% do not significantly influences the gas permeability (P) except for CO2. The PDMS matrix appears to be highly permeable and, therefore, a decreasing effect on P is only marked for a very high HTiNbO5 content. This effect is more pronounced for CO2, the P value of which decreases by 80% when the amount of nanofiller is 40 wt.%. The sorption measurements show that the interaction between CO2 and PDMS is weak (isotherms agree with Henry’s law). The filler decreases the solubility of CO2 in the films (S = 7.94 × 10−3 and S = 5.44 × 10−3 cm3 STPcm−3 film cmHg−1 for PDMS and PDMS-HTiNbO5 40 wt.%, respectively). 相似文献
85.
The apparent solubility (S), concentration-average diffusivity (D), and permeability (P), for C0_2, CH_4 and N_2 through PPO and aryl-brominated PPO at 35℃for pressure ranging from 1 to 26 atm are reported. It is found that P, D, and S of the membranes to all the three gases vary with the extent of bromination. S increases with the increase of the percent of bromine in each case, but D to CO_2 increases remarkably only at higher degree of brominafion, and therefore, P to CO_2 is increased by more than 100% over a wide range ofpressure in the case. The solubility data are well described by the dual mode sorption model. It is found that the gas molecules sorbed by the Langmuir mode are relatively more immobilized and the contribution of the nonequilibrinm character of the polymer to gas permeation increases obviously for CO_2 and is hardly changed for CH_4 with increasing bromine content. These observations are interpreted in terms of changes in specific free volume (SFV)and the cohesive energy density (CED) of the polymers. 相似文献
86.
87.
Let A be a subalgebra of Uq (sl(2)) generated by K, K-1 and F and Aδ be a subalgebra of Uq (sl(2)) generated by K, K-1 (and also Fd if q is a primitive d-th root of unity with d an odd number). Given an Aδ -module M, a Uq (sl(2))-module AAδ M is constructed via the iterated Ore extension of Uq (sl(2)) in a unified framework for any q. Then all the submodules of AAδ M are determined for a fixed finite-dimensional indecomposable Aδ -module M . It turns out that for some indecomposable Aδ -module M , the Uq (sl(2))-module AAδ M is indecomposable, which is not in the BGG-categories Oq associated with quantum groups in general. 相似文献
88.
《Analytical letters》2012,45(4):513-527
Abstract An enzyme membrane electrode usable for the assay of oxalate in foodstuffs is described. A commercially available preactivated polyamide membrane was used for the immobilization of oxalate oxidase. The bioactive disk thus obtained was associated with an amperometric transducer. The resulting self-contained enzyme electrode wich allows oxalate determination in various materials with minimal pretreatment exhibits a linear calibration ranging from 10–7 M and 10–4 M in the cell. The response-time was comprised between 20 seconds and 1 minute, depending on the oxalate content in the sample. The electrode-response was very stable for at least 4 months, a period during which more than 150 assays were performed. The results obtained with several food materials were in good agreement with those obtained with the conventional spectrophotometric method. Assays were also performed with a microprocessor-based analyzer normally used for glucose measurements with a glucose oxidase electrode When the analyzer is equipped with an oxalate oxidase membrane, without further setting, oxalate can be determined in the range 5 10?3 M-10?1 M in the sample. 相似文献
89.
Soft membranes are commonly employed in shape-morphing applications, where the material is programmed to achieve a target shape upon activation by an external trigger, and as coating layers that alter the surface characteristics of bulk materials, such as the properties of spreading and absorption of liquids. In particular, polymer gel membranes experience swelling or shrinking when their solvent content change, and the non-homogeneous swelling field may be exploited to control their shape. Here, we develop a theory of swelling material surfaces to model polymer gel membranes and demonstrate its features by numerically studying applications in the contexts of biomedicine, micro-motility, and coating technology. We also specialize the theory to thermo-responsive gels, which are made of polymers that change their affinity with a solvent when temperature varies. 相似文献
90.
Let k be an algebraically closed field of characteristic p 2, and gl(m|n) be the general linear Lie superalgebra over k. The Cartan invariants for the restricted supermodule category for gl(m|n) are presented. 相似文献