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501.
Biodiesels and biolubricants are synthetic esters produced mainly via a transesterification of other esters from bio-based resources, such as plant-based oils or animal fats. Microwave heating has been used to enhance transesterification reaction by converting an electrical energy into a radiation, becoming part of the internal energy acquired by reactant molecules. This method leads to major energy savings and reduces the reaction time by at least 60% compared to a conventional heating via conduction and convection. However, the application of microwave heating technology alone still suffers from non-homogeneous electromagnetic field distribution, thermally unstable rising temperatures, and insufficient depth of microwave penetration, which reduces the mass transfer efficiency. The strategy of integrating multiple technologies for biodiesel and biolubricant production has gained a great deal of interest in applied chemistry. This review presents an advanced transesterification process that combines microwave heating with other technologies, namely an acoustic cavitation, a vacuum, ionic solvent, and a supercritical/subcritical approach to solve the limitations of the stand-alone microwave-assisted transesterification. The combined technologies allow for the improvement in the overall product yield and energy efficiency. This review provides insights into the broader prospects of microwave heating in the production of bio-based products.  相似文献   
502.
We examine here our spectroscopic modification of the Pippard relation which is a linear variation of the thermal expansivity alpha(p) with the frequency shifts (1/nu)(partial differentialnu/partial differentialp)(T) close to the melting point in ammonia solid II. For this we use our calculated frequencies for the Raman mode of nu (51 cm(-1)) in ammonia solid II for the pressures of 3.65, 5.02 and 6.57 kbars. We establish this linearity between alpha(p) and (1/nu)(partial differentialnu/ partial differentialp)(T) for the pressures studied in ammonia solid II close to the melting point. The observed behaviour of ammonia solid II is explained in terms of our spectroscopic relation given here.  相似文献   
503.
Gezici O  Kara H 《Talanta》2011,85(3):1472-1482
The stationary phase characteristics of the material obtained through immobilization of humic acid (HA) to aminopropyl silica (APS) via amide-bond formation were investigated. The material was characterized in terms of elemental analysis, FTIR, thermogravimetric analyses, pH point of zero charge measurements, potentiometric titrations, and contact angle measurements. Amount of HA bonded to APS was determined from the elemental analysis results, and found as 170 mgHA/gAPS. Stability of the material was studied in aqueous media at different pH values, and amount of HA released at pH = 8 did not exceed 2% of the total immobilized HA. Stationary phase characteristics of the well-characterized material were investigated in an HPLC system by using some low-molecular weight polar compounds (i.e. some nucleosides and nucleobases) as test solutes. Effect of some experimental variables such as column conditioning, composition of mobile phase, and temperature on the chromatographic behavior of the studied compounds was studied. Role of ammonium solutions at different pH values on retentive properties of the species was also studied. Retention factors (k′) versus volume percentage of organic modifier exhibited a U-curve, which was evaluated as an indication for RPLC/HILIC mixed-mode behavior of the stationary phase. Orthogonality between RPLC and HILIC modes was analyzed through geometric approach, and found as 48.5%. Base-line separation for the studied groups of compounds was achieved under each studied mode, and some differentiations were observed in elution order of the compounds depending on the HPLC mode applied. Chromatograms recorded under RPLC and HILIC modes were compared with those recorded on APS under similar conditions, and thus the influence/importance of HA immobilization process was evaluated in detail. In light of the obtained results, immobilized HA is represented as a useful stationary phase for HPLC separations.  相似文献   
504.
505.
The substrate scope of the [2+2] cycloaddition-cycloreversion (CA-CR) reaction between electron-deficient (2,2-dicyanovinyl)benzene (DCVB) or (1,2,2-tricyanovinyl)benzene (TCVB) derivatives and N,N-dimethylanilino (DMA)-substituted acetylenes was investigated. The structural features of the cyanobutadiene products of these transformations were examined and the rates of selected CA-CR reactions were measured. Rate constants for reactions utilizing pentafluorinated TCVB and DCVB were found to be one to two orders of magnitude larger than those for the unsubstituted analogues. Multiple, consecutive CA-CR reactions were performed with substrates incorporating two reactive 2,2-cyanovinyl or 4-ethynylanilino sites. 1,4-Bis(2,2-dicyanovinyl)-2,3,5,6-tetrafluorobenzene and 1,4-bis[(4'-dihexylamino)phenylethynyl]benzene were selected as suitably reactive monomers for the synthesis of regular [AB] oligomers wherein the push-pull chromophores were formed in the chain-growth step. Oligomers of two types were isolated: macrocyclic [AB](n) and open-chain B[AB](n) oligomers, with n≤4.  相似文献   
506.
An off-line column preconcentration technique using a micro-column of 2,6 diacetylpyridine functionalized Amberlite XAD-4 with inductively coupled plasma mass spectrometry (ICP-MS) as a means of detection has been developed. The aim of the method was to determine rare earth elements (REEs) (La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu) in seawater. Sample solutions (2–10 mL) were passed through the column which was then washed with ultra-pure water to remove residual matrix. The adsorbed cations on the resin were eluted by using 2 mL of 0.1 mol L−1 HNO3 containing 10 ng mL−1 indium as an internal standard. The eluent was analyzed for the metal concentrations using ICP-MS. Sample pH as well as the sample and eluent flow rates were optimized. The sorption capacity of resin was determined by the batch process, by equilibrating 0.05 g of the resin with solutions of 50 mL of 25 mg L−1 of individual metal ions for 4 h at pH 6.0 at 26 °C. The sorption capacities for the resin were found to range between 47.3 μmol g−1 (for Lu) and 136.7 μmol g−1 (for Gd). Limits of detection (3σ), without any preconcentration, ranged from 2 ng L−1 to 10.3 ng L−1 (for Tm and Lu respectively). The proposed method was applied to the determination of REEs in seawater and tap water samples.  相似文献   
507.
CdSe thin films were deposited on glass substrates using Successive Ionic Layer Adsorption and Reaction (SILAR) method at room temperature and ambient pressure. The relationship between refractive index and energy bandgap was investigated. The film thickness effect on the structural, morphological, optical and electrical properties of CdSe thin films was investigated. The X-ray diffraction (XRD) and scanning electron microscopy (SEM) studies showed that all the films exhibit polycrystalline nature with hexagonal structure and are covered well with glass substrates. The crystalline and surface properties of the films improved with increasing film thickness. The optical absorption studies revealed that the films are found to be a direct allowed transition. The energy bandgap values were changed from 1.93 to 1.87 eV depending on the film thickness. The electron effective mass (me?/mo), refractive index (n), optical static and high frequency dielectric constant (εo, ε) values were calculated by using the energy bandgap values as a function of the film thickness. The resistivity of the films changed between 106 and 102 Ω-cm with increasing film thickness at room temperature.  相似文献   
508.

The acid-catalyzed hydrolysis of 2-oxo-3-(p-substituted)-phenyl-5-methyl-1,2,3-oxathiazolidines (1) have been studied in 60% (v/v) 1,4 dioxane-aqueous solutions of perchloric and hydrochloric acids at 10.0 ± 0.05°C. The analysis of the kinetic data by the order of the catalytic effects of the acids, activation parameters, kinetic solvent isotope effect, and substituent effect are all in agreement with an A-2 mechanism in the studied range.  相似文献   
509.
In this paper, a novel method, named the consistent Burgers equation expansion (CBEE) method, is proposed to solve nonlinear evolution equations (NLEEs) by the celebrated Burgers equation. NLEEs are said to be CBEE solvable if they are satisfied by the CBEE method. In order to verify the effectiveness of the CBEE method, we take (2+1)-dimensional Burgers equation as an example. From the (1+1)-dimensional Burgers equation, many new explicit solutions of the (2+1)-dimensional Burgers equation are derived. The obtained results illustrate that this method can be effectively extended to other NLEEs.  相似文献   
510.
This paper studies the dynamics of optical solitons with parabolic and dual-power law nonlinearities. The dark 1-soliton solution is first obtained by the ansatz method along with the necessary constraint conditions, for both of these nonlinearities. Subsequently, the invariance, conservation laws and double reductions of the governing nonlinear Schrödinger's equation are studied and the conserved densities are thus revealed.  相似文献   
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