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1.
你可以使用一个4060B二进制计数器/振荡器制成一个简单而又准确的长迟延定时器(如图1)。该图所示的电路能够比普遍集成电路定时器提供更长的迟延时间,一般从几毫秒到数小时。输入端的正逻辑电平将计数器置于复位状态,输出端的正逻辑电平将计数器置于低度状态。当输入 相似文献
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Adamovich MI Aggarwal MM Alexandrov YA Ameeva ZV Andreeva NP Anzon ZV Arora R Badyal SK Bhalla KB Bhasin A Bhatia VS Bubnov VI Burnett TH Cai X Chasnikov IY Chernova LP Chernyavski MM Dressel B Eligbaeva GZ Eremenko LE Friedlander EM Gadzhieva SI Gaitinov AS Ganssauge ER Garpman S Gerassimov SG Gill A Grote JG Gulamov KG Gulyamov UG Gupta VK Hackel S Heckman HH Haung H Judek B Kachroo S Kadyrov FG Kalyachkina GS Kanygina EK Kaul GL Kaur M Kharlamov SP Koss T Kumar V Lal P Larionova VG 《Physical review letters》1990,65(4):412-415
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A technique for automatic anatomically selective enhancement of digital chest radiographs is developed. Anatomically selective enhancement is motivated by the desire to simultaneously meet the different enhancement requirements of the lung field and the mediastinum. A recent peak detection algorithm and a set of rules are applied to the image histogram to determine automatically a gray-level threshold between the lung field and mediastinum. The gray-level threshold facilitates anatomically selective gray-scale modification and/or unsharp masking. Further, in an attempt to suppress possible white-band or black-band artifacts due to unsharp masking at sharp edges, local contrast adaptively is incorporated into anatomically selective unsharp masking by designing an anatomy-selective emphasis parameter which varies asymmetrically with positive and negative values of the local image contrast 相似文献
5.
The kinetic behaviour of Cl(-), Br(-) and SCN(-) exchanges on hydrous tin oxide have been investigated under conditions of particle diffusion and the limited bath technique. Values for the diffusion coefficients, energy of activation and entropy of activation have been calculated. The data obtained have been compared with those reported for other organic and inorganic exchangers. 相似文献
6.
Ong LG Abd-Aziz S Noraini S Karim MI Hassan MA 《Applied biochemistry and biotechnology》2004,118(1-3):73-79
The oil palm sector is one of the major plantation industries in Malaysia. Palm kernel cake is a byproduct of extracted palm
kernel oil. Mostly palm kernel cake is wasted or is mixed with other nutrients and used as animal feed, especially for ruminant
animals. Recently, palm kernel cake has been identified as an important ingredient for the formulation of animal feed, and
it is also exported especially to Europe, South Korea, and Japan. It can barely be consumed by nonruminant (monogastric) animals
owing to the high percentages of hemicellulose and cellulose contents. Palm kernel cake must undergo suitable pretreatment
in order to decrease the percentage of hemicellulose and cellulose. One of the methods employed in this study is fermentation
with microorganisms, particularly fungi, to partially degrade the hemicellulose and cellulose content. This work focused on
the production of enzymes by Aspergillus niger and profiling using palm kernel cake as carbon source. 相似文献
7.
The reduction of 2,6-dichlorophenolindophenol (DCPI) by sulphides and sulphites has been studied kinetically by the stopped-flow technique. The reaction is first-order with respect to each of the reactants. From the distribution diagrams for the species DH(+)(2), DH and D(-) for DCPI and H(2)Q, HQ(-) and Q(2-) for sulphides or sulphites, a mechanism is proposed which suggests partial reactions of all possible combinations of the reacting species at any pH. An equation for calculation of the second-order reaction rate constants k at any pH is derived, which gives k as a function of [H(+)], the partial reaction rate constants and the dissociation constants of DCPI and H(2)S or H(2)SO(3). Values of the overall reaction rate constants over a wide pH-range have been determined, together with values of k for all possible partial reactions. For particular pH-values the second-order reaction rate constant was determined by four different methods. Mean values of k = 251 +/- 1 and 240 +/- 1 l.mole(-1).sec(-1) were obtained for pH 3.15 and 4.17, respectively, for the DCPI-Na(2)S reaction and k = 137 +/- 1, 127 +/- 1 and 136 +/- 1 l.mole(-1).sec(-1) for pH 2.02, 4.25 and 5.10, respectively, for the DCPI-Na(2)SO(3) reaction. From the slopes of the linear Arrhenius plots activation energies of 6.6 +/- 0.2 and 4.0 +/- 0.1 kcal/mole for the DCPI-Na(2)S and DCPI-Na(2)SO(3) reactions, respectively were calculated. The effect of ionic strength on the reactions supports the proposed mechanism. 相似文献
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Mangos MM Min KL Viazovkina E Galarneau A Elzagheid MI Parniak MA Damha MJ 《Journal of the American Chemical Society》2003,125(3):654-661
The ability of modified antisense oligonucleotides (AONs) containing acyclic interresidue units to support RNase H-promoted cleavage of complementary RNA is described. Manipulation of the backbone and sugar geometries in these conformationally labile monomers shows great benefits in the enzymatic recognition of the nucleic acid hybrids, while highlighting the importance of local strand conformation on the hydrolytic efficiency of the enzyme more conclusively. Our results demonstrate that the duplexes support remarkably high levels of enzymatic degradation when treated with human RNase HII, making them efficient mimics of the native substrates. Furthermore, interesting linker-dependent modulation of enzymatic activity is observed during in vitro assays, suggesting a potential role for this AON class in an RNase H-dependent pathway of controlling RNA expression. Additionally, the butyl-modified 2'F-ANA AONs described in this work constitute the first examples of a nucleic acid species capable of eliciting high RNase H activity while possessing a highly flexible molecular architecture at predetermined sites along the AON. 相似文献
10.
A simple method has been developed for the simultaneous determination of N-butylscopolamine bromide and oxazepam in pharmaceutical formulations using first-order digital derivative spectrophotometry. Acetonitrile was selected as the solvent in which both compounds showed well-defined bands. Both analytes showed good stability in this solvent when solutions of the analytes were exposed to light and temperatures between 20 degrees and 80 degrees C. The simultaneous determination of both drugs was performed by the zero-crossing method at 226.0 and 257.0 nm for N-butylscopolamine and oxazepam, respectively. The linear range of determination was found to be 2.5 x 10(-7) to 8.0 x 10(-5) mol/L for N-butylscopolamine and 7.1 x 10(-8) to 8.0 x 10(-5) mol/L for oxazepam. A very good level of repeatability (relative standard deviation) of 0.2% was observed for N-butylscopolamine and oxazepam. The ingredients commonly found in pharmaceutical formulations do not interfere. The proposed method was applied to the determination of these drugs in pharmaceutical formulations (capsules). 相似文献