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991.
A. Dávid G. Horváth Z. Mészáros T. Meisel Z. Halmos 《Journal of Thermal Analysis and Calorimetry》1974,6(1-2):59-66
The thermal behaviour of tetrahydroperparine (THP) and its derivatives with various acids has been investigated. The acid is liberated from the formate derivative basically in two steps, while the other aliphatic acids are released quantitatively before the thermal decomposition of the THP molecule. The thermoanalytical curves, electrical conductivity data measured in the molten phase, and infrared spectra prove that while part of the formic acid is hydrogen-bonded the other part is bound ionically in the molecule. It may be assumed that the marked biological activity of the compound can be explained by this difference in the nature of the bonds. 相似文献
992.
J R J Delben D R Chaves P D Candelorio A A S T Delben 《Journal of Thermal Analysis and Calorimetry》2006,83(2):411-414
New glasses have been synthesized in the system ZrF46BaF26PrF3. Glasses were prepared by conventional fusion method and the
vitreous domain was established. For vitreous samples the thermal stability
parameters were determined, so that the best compositions could be selected
according to a compromise between high glass forming ability and thermal stability
vs. crystallization. 相似文献
993.
A system was designed to automate the determination of three image dyes in an instant photographic material. The method involves extracting negative samples with dimethylsulfoxide and filtering the extract, followed by quantitating the dye coverage (dye per unit area of negative) through a spectrophotometric flow-injection procedure. Significant spectral overlap exists among the dyes, and as a result calculation of coverage requires solving three simultaneous equations. A microcomputer and data acquisition system were employed for controlling the detector and flow-injection system, acquiring and integrating the detector response, calculating coverage, producing and displaying control charts, and automatically transferring results to a VAX based corporate database. In addition to automating sample preparation and measurement steps as much as possible, the goal of this project was to automate the data manipulation and transfer steps. 相似文献
994.
Martin B. Hocking David T. Syme David E. Axelson Kirk H. Michaelian 《Journal of polymer science. Part A, Polymer chemistry》1990,28(11):2969-2982
The comonomer required, p-maleimidobenzoic acid (MBA) was first prepared in good yield by refinements of published methods. p-Carboxysuccinanilic acid (CSA), and p-succinimidobenzoic acid (SBA), were also prepared to provide models useful for IR and NMR for spectroscopic assignments of the new copolymers. Polymerization of MBA with acrylamide in glacial acetic acid at 60°C gave copolymers with estimated viscosity average molecular weights of 60,000 to 90,000. Yields and viscosity average molecular weights decreased as the MBA to acrylamide monomer feed ratio was increased. The rate of incorporation of MBA into the copolymer rose from 7 to 23% when the mole ratio in the feed was raised from 5 to 20%. Decreasing the initiator concentration increased molecular weights by less than predicted and reduced the yield of copolymer for any given feed ratio of MBA to acrylamide. In all cases about 30–40% of the MBA units in the purified copolymers were hydrolyzed. A change to dimethyl sulfoxide solvent gave good, and poor yields of copolymer at 5 and 10 mol % MBA, respectively, and no copolymer at 20 mol % MBA. Viscosity average molecular weights of the copolymer products prepared in DMSO were somewhat lower than obtained for the copolymers prepared in acetic acid. Polymerization in a DMSO-water mixture gave a negligible yield of polymeric product. Instead, only hydrolysates of MBA precipitated when the coloured polymerization solutions were added to methanol. 相似文献
995.
V. Ščasnár L. Beneš Š. Bezek T. Trnovec 《Journal of Radioanalytical and Nuclear Chemistry》1984,82(2):287-297
Simple and rapid extraction method for quantitative and selective isolation of the new local anesthetic pentacaine from biological materials is proposed. The technique of ion-pair formation was found to be more effective than usual access using the extraction of the nonionized species. The extraction yield of the unchanged molecule3H-pentacaine after double extraction and single scrubbing was found to be more than 90%. The radiochemical purity was over 90%. The method appears suitable for pharmacokinetic studies in the animal body. 相似文献
996.
A study of the substoichiometric extraction of phosphorus is described. Phosphorus was extracted in the form of ternary compounds
such as ammonium phosphomolybdate, 8-hydroxyquinolinium phosphomolybdate, tetraphenylarsonium phosphomolybdate and tri-n-octylamine
phosphomolybdate. Consequently, phosphorus was extracted substoichiometrically by the addition of a substoichiometric amount
of molybdenum for all four phosphomolybdate compounds. On the other hand, phosphorus could be separated substoichiometrically
with a substoichiometric amount of tetraphenylarsonium chloride or tri-n-octylamine. Stoichiometric ratios of these ternary
compounds obtained substoichiometrically were 1∶12∶3 for phosphorus, molybdenum and organic reagent. Applicability of these
compounds to phosphorus determination was also discussed. 相似文献
997.
The polymerization of acrylonitrile (AN) initiated by oxygen-ascorbic acid (AA)-ferric ion system was studied in dil. HNO3 at 40°. The rate of polymerization, Rp, was found gravimetrically. In the [Fe3+] range, (2–5 × 10?5 M, Rp was proportional to [AN]1.5 ± 0.05, [O2]0.5 ± 0.02 [AA]0 and [Fe3+]0; for [Fe3+] = (5–30) × 10?5 M, it was proportional to [AN]1.8 ± 0.05, [O2]0.6 ± 0.02, [AA]0 and [Fe3+]?0.9 ± 0.05. A plausible reaction scheme is proposed and rate law presented to explain these results. Rp increased with ionic strength and [HNO3] (up to ~0.25 M). An initial rate increase with temperature followed by a decrease was noticed. Chain lengths of the polymers were determined viscometrically. 相似文献
998.
High performance liquid chromatography followed by post-column reaction detection in the far-red spectral region provides added sensitivity and selectivity. A homogeneous fluorescence energy transfer assay in the competitive mode based on the binding of biotin and streptavidin was developed as an on-line post-column reaction detection system. The labels used for energy transfer were R-Phycoerythrin conjugated to biotin and Cyanine 5 labeled with streptavidin. The energy transfer peak was measured at 670 nm and excitation was achieved using the 488 nm line of an argon ion laser. The biotin concentration in plasma ultrafiltrate ranged from 0.024 to 6.12 ng/mL (n = 6). The precision of the two controls, 0.24 and 2. 44 ng/mL, was found to be 18.70% and 9.92% relative standard deviation respectively. Accuracy was 10.47% and 1.95% difference from spiked, respectively (n = 6). The limit of detection was 21.70 pg/mL (8.90 x 10(-11)M) calculated based on a factor of 2x the standard deviation of the blank (n = 6). The correlation coefficient for the calibration curve was found to be 0.9995. Recovery from plasma ultrafiltrate at 2.44 ng/mL was 103.40% (n = 6). Detection selectivity was indicated by the absence of background fluorescence in six different plasma samples collected from six individual donors. Endogenous levels were detected in two of the six pools of plasma ultrafiltrates. 相似文献
999.
Sergeev GB Shabatina TI Solov'ev VN Nemukhin AV 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2000,56(13):2527-2537
The results on spectroscopic study of low temperature interactions of metal atoms, small clusters and nanoparticles with different organic and inorganic substances in the temperature range 12-300 K are presented. Complexation and reactions of atoms and clusters of magnesium, samarium and silver with carbon dioxide, ethylene and some mesogenic cyanophenyls were studied by the technique of matrix isolation and low temperature co-condensation of metal and ligand vapors, low temperature UV-Vis, IR- and ESR-spectroscopy in combination with quantum chemistry calculations. It was shown that cryochemical reactions of metal particles of different sizes reflected the system's redundant energy. 相似文献
1000.
Molander P Haugland K Hegna DR Ommundsen E Lundanes E Greibrokk T 《Journal of chromatography. A》1999,864(1):103-109
Sub-ambient column temperatures, promoting strong interactions between the analyte and the stationary phase material, were utilized to focus large volumes of the polyolefin antioxidant Irganox 1076 [benzenepropanoic acid, 3.5-bis(1,1-dimethylethyl)-4-hydroxy-, octadecyl ester] on the column inlet, using pure acetonitrile as sample solvent and mobile phase. Injection volumes up to 100 microl were successfully employed on a 50 cm x 320 microm I.D. capillary column packed with 5 microm Kromasil 100 ODS particles. Irganox 1076 was eluted after completed injection by temperature programming, using a temperature program from 7 to 90 degrees C, in 3 degrees C min(-1). UV detection, using a low-dispersion "U"-shaped flowcell, was performed at 280 nm. The method was applied for the determination of Irganox 1076 that was extracted from low-density polyethylene (0.6 ppm, w/w). Both Soxhlet and microwave-aided solvent extractions were performed, using chloroform and acetonitrile as solvents, respectively. The microwave-aided extraction with acetonitrile was found to give approximately the same yield as the standard Soxhlet reference method. Consequently, small volumes of acetonitrile could be used both as extraction solvent, sample solvent and mobile phase, simplifying the analysis process. The mass limit of detection of the method was found to be 3.3 ng, corresponding to a concentration limit of detection of 33 ng ml(-1), utilizing an injection volume of 100 microl. The within and between day precision of retention times displayed relative standard deviations below 1.2%. 相似文献