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排序方式: 共有672条查询结果,搜索用时 15 毫秒
1.
Anuradha Sharma Gurmeet K. Bakshi Madhu Raka 《Finite Fields and Their Applications》2007,13(4):1071-1085
Polyadic codes constitute a special class of cyclic codes and are generalizations of quadratic residue codes, duadic codes, triadic codes, m-adic residue codes and split group codes, which have good error-correcting properties. In this paper, we give necessary and sufficient conditions for the existence of polyadic codes of prime power length. Examples of some good codes arising from the family of polyadic codes of prime power length are also given. 相似文献
2.
Madhu V. Nayakkankuppam 《Mathematical Programming》2007,109(2-3):477-504
We describe an approach to the parallel and distributed solution of large-scale, block structured semidefinite programs using
the spectral bundle method. Various elements of this approach (such as data distribution, an implicitly restarted Lanczos
method tailored to handle block diagonal structure, a mixed polyhedral-semidefinite subdifferential model, and other aspects
related to parallelism) are combined in an implementation called LAMBDA, which delivers faster solution times than previously
possible, and acceptable parallel scalability on sufficiently large problems.
This work was supported in part by NSF grants DMS-0215373 and DMS-0238008. 相似文献
3.
Frank N. Proske Madan L. Puri 《Proceedings of the American Mathematical Society》2003,131(9):2937-2944
In this article we prove a strong law of large numbers for Borel measurable nonseparably valued random elements in the case of generalized random sets.
4.
5.
A highly selective, sensitive, and fairly rapid and economical differential pulse polarographic (DPP) method has been reported for the determination of trace amounts of vanadium and molybdenum in standard alloys and various environmental samples. The morpholine-4-carbodithioates of these metals were retained (>99% recovery) quantitatively on microcrystalline naphthalene in the pH range 4.5-6.9 for vanadium and 1.5-4.5 for molybdenum. These metals were determined by DPP after desorption with 10 ml of 1 M HCl. Vanadium and molybdenum may also be preconcentrated by passing their aqueous solutions under similar conditions on morpholine-4-dithiocarbamate CTMAB-naphthalene adsorbent packed in a column at a flow rate of 1-5 ml min(-1) and determined similarly. The detection limits are 0.20 ppm for vanadium and 0.04 ppm for molybdenum at minimum instrumental settings (signal to noise ratio=2). The linearity is maintained in the following concentration ranges, vanadium 0.50-10.0 and molybdenum 0.10-9.0 ppm, with a correlation factor of 0.9996 (confidence interval of 95%, slopes 0.0196 and 0.01497 muA mug(-1), intercepts 3.65x10(-3) and -1.92x10(-3) respectively) and relative standard deviation of 1.1% in the microcrystalline method, while in the column method, the linearity is maintained in the concentration ranges, 0.50-6.5 for vanadium and 0.10-5.5 ppm for molybdenum with correlation factor of 0.9994 (with confidence interval of 95%, slopes 0.0194, 0.015 muA mug(-1), intercepts 3.60x10(-3) and -1.90x10(-3) respectively) and relative standard deviation of 1.4%. Various parameters such as the effect of pH, reagent, naphthalene and CTMAB concentrations, volume of aqueous phase and interference of a large number of metal ions on the estimation of vanadium and molybdenum have been studied in detail to optimize the conditions for their voltammetric determination at trace level in various standard alloys and environmental samples. 相似文献
6.
A column preconcentration method has been developed for the determination of trace amounts of manganese by preconcentration on 2-nitroso-1-naphthol-4-sulfonic acid (nitroso-S)-tetradecyldimethylbenzylammonium (TDBA) naphthalene as an adsorbent using a simple funnel tipped glass tube. Manganese reacts with nitroso-S to form a water soluble brown colored chelate anion. The chelate anion forms a water insoluble Mn-Nitroso-S-TDBA ion pair on naphthalene packed in a column in the pH range 9.6-10.5 at a flow rate of 1-2 ml/min. The solid mass consisting of manganese complex and naphthalene is dissolved in 5 ml of dimethylformamide (DMF) and the metal determined by second derivative spectrophotometry. The calibration curve is linear in the concentration range 0.25-35.0 micrograms of Mn in 5 ml of the final DMF solution. Eight replicate determinations of 25 micrograms of standard manganese solution give a mean peak height of 4.0 with a correlation coefficient of 0.9995 and relative standard deviation of +/- 1.1%. The sensitivity was calculated to be 0.502(d2 A/d lambda 2)/microgram ml-1 from the slope of the calibration curve. The detection limit was 0.020 microgram ml-1 for manganese at the minimum instrumental settings (signal to noise ratio = 2). Various parameters effecting the method such as the effect of pH, volume of aqueous phase and interference of a number of metal ions on the determination of manganese have been evaluated to optimize the conditions for its determination in standard alloys and biological samples. 相似文献
7.
A highly selective, sensitive and rapid differential pulse polarographic method (DPP) has been developed for the simultaneous estimation of trace amounts of lead and cadmium in standard alloys, biological and environmental samples. The morpholine-4-carbodithioates of the samples were absorbed on microcrystalline naphthalene in the pH range of 5-10 for lead and 3.4-11 for cadmium. The metal complexes were desorbed with 10 ml of 1M HCl and determined simultaneously with a differential pulse polarograph. These metals can alternatively be quantitatively adsorbed on morpholine-4-dithiocarbamate-cetyltrimethylammonium bromide-naphthalene adsorbent packed in a column and determined similarly. The detection limits are 0.14 ppm for Pb and 0.014 ppm for Cd at minimum instrumental settings (signal-to-noise ratio = 2). The linearity is maintained in the concentration ranges of Pb, 0.7-15 ppm and Cd, 0.07-10 ppm with a correlation factor of 0.9997 and relative standard deviations of 0.95 and 0.81%, respectively. Various parameters such as the effect of pH, volume of aqueous phase, and interference of a number of metal ions on the estimation of lead and cadmium have been studied in detail to optimize the conditions for their simultaneous estimation in various biological and environmental samples. 相似文献
8.
N-methylethylxanthocarbamate has been used as an analytical reagent for the determination of trace amounts of cadmium in standard alloys, biological, and environmental samples. The reagent has been found to form a water insoluble complex with cadmium. It is quantitatively adsorbed over microcrystalline naphthalene in the pH range 2.5 to 12.0. The metal complex is desorbed with HCl and cadmium determined with a differential pulse polarograph. The detection limit is 0.05 ppm (signal-to-noise ratio = 2) and the linearity is maintained in the concentration range 0.2–25 g/ml, with correlation coefficient of 0.9995 and a relative standard deviation of ±0.81%. Characterization of the electroactive process includes an examination of the degree of reversibility. Various parameters, such as the effect of pH, reagent concentration, amount of naphthalene, volume of aqueous phase, and the interference of a large number of metal ions on the determination of cadmium, have been studied in detail to optimize the conditions for its determination in various complex materials. 相似文献
9.
N. T. Madhu P. K. Radhakrishnan W. Linert 《Journal of Thermal Analysis and Calorimetry》2006,84(3):607-611
The
phenomenological, kinetic and mechanistic aspects of the nitrate, chloride,
bromide and iodide complexes of nickel(II) with1,2-(diimino-4’-antipyrinyl)ethane
(GA) have been studied by TG and DTG techniques. The kinetic parameters like
activation energy, pre-exponential factor and entropy of activation were computed.
The rate controlling process in all stages of decomposition is random nucleation
with one nucleus on each particle (Mampel model). 相似文献
10.
Cobalt-2-(5-bromo-2-pyridylazo)-5-diethylaminophenol (5-Br-PADAP)-tetraphenylborate ion associated complex is quantitatively adsorbed on microcrystalline naphthalene in the pH range 3.5-9.5 from a fairly large volume of the aqueous samples (preconcentration factor ~30). After filtration, the solid mass consisting of the cobalt complex and naphthalene was dissolved with 5 ml of dimethylformamide (DMF) and the metal determined by first-derivative spectrophotometry. The cobalt-5-Br-PADAP complex can alternatively be quantitatively retained on ammonium tetraphenylborate-naphthalene adsorbent filled in a column (preconcentration factor 120) in the same pH range and determined similarly. The detection limit is 30 ppb (signal-to-noise ratio=2) and the calibration curve is linear over 0.3-8.0 mug of cobalt in 5 ml of the final DMF solution. Eight replicate determinations of 1.0 mug of cobalt gave a mean peak height of 0.208 (at 611.5 nm) with a relative standard deviation of 1.2%. The sensitivity of the method is 1.04 (dA/dnm) ml mug(-1) found from the slope of the calibration curve. The interference of a large number of anions and cations on the determination of cobalt has been studied and the optimized conditions developed were utilized for its trace determination in various standard alloys and biological samples. 相似文献