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991.
Summary This paper continues earlier work by the same authors concerning the shape and size of the stability regions of general linear discretization methods for initial value problems. Here the treatment is extended to cover also implicit schemes, and by placing the accuracy of the schemes into a more central position in the discussion general method-free statements are again obtained. More specialized results are additionally given for linear multistep methods and for the Taylor series method.This research has been supported by Swiss National Foundation, Grant No. 82-524.077This research has been supported by the Heinrich-Hertz-Stiftung, B 32 No. 203/79 相似文献
992.
W. Höhn 《Numerische Mathematik》1982,40(2):207-227
Summary Several regularization methods for parabolic equations backwards in time together with the usual additional constraints for their solution are considered. The error of the regularization is estimated from above and below. For a boundary value problem in time-method, finite elements as well as a time discretization are introduced and the error with respect to the regularized solution is estimated, thus giving an overall error of the discrete regularized problem. The algorithm is tested in simple numerical examples. 相似文献
993.
C. I. Goldstein 《Numerische Mathematik》1982,38(1):61-82
Summary The finite element method with non-uniform mesh sizes is employed to approximately solve Helmholtz type equations in unbounded domains. The given problem on an unbounded domain is replaced by an approximate problem on a bounded domain with the radiation condition replaced by an approximate radiation boundary condition on the artificial boundary. This approximate problem is then solved using the finite element method with the mesh graded systematically in such a way that the element mesh sizes are increased as the distance from the origin increases. This results in a great reduction in the number of equations to be solved. It is proved that optimal error estimates hold inL
2,H
1 andL
, provided that certain relationships hold between the frequency, mesh size and outer radius. 相似文献
994.
《Arabian Journal of Chemistry》2022,15(12):104368
Protein hydrolysates have the potential to be natural and safer sources of bioactive peptides. In this study, two proteases were used to hydrolyze Chinese sturgeon (Acipenser sinensis) protein, and the hydrolysates were then purified to yield antioxidant peptides. The degree of hydrolysis of 23.56 % and 18.14 % was obtained using papain and alcalase 2.4L, respectivly, and hydrolysates had 96.80 % and 87.24 % total amino acid content, respectivly. The papain hydrolysate (PH) and alcalase 2.4L hydrolysate (AH) showed good antioxidant activity against DPPH? (IC50 of 3.64 and 3.15 mg/mL) and ABTS?+ (IC50 of 1.92 and 1.58 mg/mL), respectively. The low-molecular-weight (<1000 Da) fraction of both hydrolysates demonstrated the highest antiradical activity (IC50 of 2.59 and 2.31 mg/mL, DPPH) and (IC50 of 1.54 and 1.36 mg/mL, ABTS), respectively. Nine peptides were separated from both hydrolysates using reverse phase high performance liquid chromatography (RP-HPLC). The IC50 for ABTS?+ scavenging activity of peptide P5 with valine, glycine and asparagine (MW of 282.13 Da) from PH, and peptide P3 with histidine, glycine and alanine (MW of 302.74 Da) from AH was 0.89 and 0.72 mg/mL, respectively. The fractions and purified peptides obtained from Chinese sturgeon hydrolysates could be utilized as natural antioxidant substitutes in pharmaceuticals and food products. 相似文献
995.
Graphite arc emission spectrometry has become possible as a result of the invention of novel types of optical spectrometers
with Echelle-optics and semiconductor array detectors, and by the application of electronically controlled, high current arc
generators. An optimization of the excitation parameters to boron carbide analysis is reported here, measuring background
corrected line intensities that were integrated for the time of total evaporation of 5 mg boron carbide sample with or without
added chemical modifiers. The following set of experimental conditions were compared with respect of analytical sensitivity
and precision: (A) no modifier, Ar + O2 (20%), 16 A; (B) sample + graphite powder (1 + 1), Ar + O2 (20%), 16 A; (C) sample + CaF2 (1 + 1), Ar, 25 A; (D) sample + CaF2 + graphite powder (1 + 1 + 1), Ar, 25 A. The graphite powder modifier resulted in improved precision in general, and the
CaF2 was effective as a plasma ionization buffer and fluorinating agent. The best compromise was found under conditions B, when
oxygen was present in the discharge atmosphere. This is likely due to the stepwise conversion of the boron carbide matrix
to the more volatile boron oxide. Under conditions B, detection limits in the ranges of 0.3–9 μg g−1 for Al, Ca, Cr, Cu, Fe, Mg, Mn and Si and that of 18–38 μg g−1 for Ti, W, and Zr were attained. Average RSDs of 10.2 and 9.7% were found, respectively, without and with internal referencing
to boron. 相似文献
996.
A system has been developed for online preconcentration and determination of Cd using thermospray flame furnace atomic absorption
spectrometry (TS-FF-AAS). It is based on the solid-phase extraction of Cd in an Amberlite XAD-2 minicolumn loaded with 2-(2-thiazolylazo)-5-dimethylaminophenol
(TAM), and the metal ion is eluted with 1 mol L−1 hydrochloridric acid, followed by its determination. The online system allows determining Cd with a detection limit of 8.0 ng L−1 and a quantification limit of 25.0 ng L−1. The precision (repeatability), calculated as the relative standard deviation (% RSD) in sample solutions containing 0.5
and 3.0 μg L−1 of Cd, was 6.1 and 4.5%, respectively. The preconcentration factor obtained was 24. The system’s accuracy was confirmed by
analyzing the following certified reference materials (CRMs): Rice flour NIES 10b, Apple leaves NIST 1515 and Orchard leaves
NBS 1571. This procedure was applied to the determination of Cd in cabbage and powdered guarana samples. 相似文献
997.
An analytical method using alumina modified with water-soluble polyacrylic acid polymer for the simultaneous separation and
preconcentration of trace Cu and Cd in a column system, and their determination by flame atomic absorption spectrometry was
developed. The conditions for coating Al2O3 with polyacrylic acid were optimized, then the column was packed with 50 mg of this sorbent. Cd and Cu solution was passed
through a glass column at pH 4.5, and elution was carried out with 5 mL of 0.05 M HCl at a flow rate of 1 mL min−1. A sorption capacity of 10 mg Cu and 12 mg Cd was obtained for 1 g sorbent. The detection limit was calculated as 4.5 μg L−1 for Cu and 1.54 μg L−1 for Cd in the final solution. Enrichment factors of 300 for Cd and 400 for Cu were obtained. 相似文献
998.
A coulometric procedure has been developed by which 18 to 240 μg quantities of bromate may be determined to within 0.3 μg. The bromate is allowed to react with bromide in an acid solution and electrolytically generated cuprous copper is used for the titration. A dual platinum electrode indicator system is used in an amperometric end-point procedure 相似文献
999.
T.F. Wynn P. Clardy L. Vaughn J.D. Bradshaw J.N. Bower M.S. Epstein J.D. Winefordner 《Analytica chimica acta》1981,124(1):155-161
A system for measuring atomic fluorescence of atoms produced via an electrically-heated graphite filament in a flame (acetylene/air or acetylene/nitrous oxide) and excited with a 300-W Eimac xenon are lamp is described. The experimental system also included wavelength modulation for background emission/fluorescence/scatter correction and an optically-triggered electronic integrator for efficient monitoring of the analyte fluorescence signal. Copper, aluminum and molybdenum were determined in jet engine lubricating oil samples (1 μl) with no pretreatment. The determinations are evaluated with respect to the accuracy and repeatability criteria of the U.S. Joint Oil Analysis Program. 相似文献
1000.
José Neri G.?Paniz érico Marlon de M.?Flores Ayrton F.?MartinsEmail author 《Mikrochimica acta》2005,152(1-2):89-92
With the aim of avoiding cumbersome sample treatment, we present a device for the introduction of solid soil samples into
AAS-flames for gold determination, as well as the proposition of earth from anthills as a gold occurrence indicator. A previous
ground sample of anthill earth (0.50 mg) was weighed directly into a small recipient of polyethylene which was then connected
to a sampling boronsilicate glass chamber. The sample was carried by an airflow (5 L min−1) to a quartz cell positioned between the burner top and the optical beam. The generated atomic vapor produced a transient
signal which was totally integrated in three seconds. The performance was compared with conventional flame atomic absorption
spectrometry after proper sample digestion. No significant differences were observed between both procedures (mean deviation
±1.90%), and a LOQ of 0.03 μg Au was achieved using the proposed method. The anthill earth was found to be very suitable for
indication of gold occurrence in soils and related materials. 相似文献