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31.
Summary In this paper, polymeric hollow fibers prepared from pH-stable polypropylene were used as columns for micellar electrokinetic
capillary chromatography (MECC). The electroosmotic flow (EOF) for polypropylene hollow fibers was evaluated in the pH range
of 5.0–12.0. With untreated polypropylene hollow fibers a stabilized but enhanced EOF was achieved when SDS was used in the
buffer, decreasing the separation window for uncharged substances in MECC to impractical levels. Uncharged acrylamide and
charged 2-acryloylamido-2-methylpropane sulfonic acid surface modifications were used to lower the strength of the EOF, increase
the separation window and prevent local overheating that could melt the column wall. 相似文献
32.
Supercritical fluid chromatography using flameless sulfur chemiluminescence detection has been investigated for the analysis of sulfur compounds in petroleum products. The chromatography and detection system was easy to implement and exhibited good precision, linearity, selectivity, and sensitivity. A minimum detectable limit of 0.3 pg sulfur/s was obtained, and response to sulfur in different sulfur species was nearly equimolar. 相似文献
33.
34.
Summary A program is described which calculates the number of effective plates and the coating efficiency over the entire range of a test chromatogram. The peak widths at half height are derived by assuming a Gaussian peak shape. The interpolated peak width at k=4 is used for computing a standardized number of effective plates. Plate height, column permeability, overall performance and a novel parameter called sampling efficiency are calculated from 5 other figures — i. e. carrier gas code, pressure drop, column length, column temperature and particle size.Dedicated to Dr. Leslie S. Ettre for his 60th birthday. 相似文献
35.
Summary A flow-through two electrode wall-jet cell with a platinum measuring electrode and a cell volume of 20 nl has been designed and evaluated. It has been used to detect phenols by reversed phase liquid chromatography using short micro bore columns. The linear dynamic range between the measured current and the concentration is greater than 103 (1.5×10–7–5×10–4 mol/l) and the minimum analyzable amount was found to be 10 pg for pyrocatechol. A negligible broadening in the detector permits the use of micro columns down to 0.5 mm internal diameter, packed with 5 m particles, without any substantial distortion of eluted zones.Presented at the 14th International Symposium on Chromatography London, September, 1982 相似文献
36.
An application of coupled column ion chromatography (IC)-inductively coupled plasma mass spectrometry (ICP-MS) is presented for speciation of chromium in waste waters. By coupling an anion column with a cation column, both the cationic Cr(III) and anionic Cr(VI) species can be analyzed with detection limits below 0.5 μg/1. The separation of the interfering ions (chloride, chlorate, perchlorate, sulphate, sulphite, sulphide, thiosulphate, carbonate, cyanide and some organic compounds) from the chromium peaks is discussed, and the use of different chromium isotopes for data acquisition is compared. Based on the results, m/z 52 was considered as an ideal isotope for speciation of chromium in waste waters by the coupled column IC-ICP-MS, because it did not suffer from polyatomic interferences and due to the high sensitivity for chromium. The analysis of the waste water samples should be performed as soon as possible after sampling according to the stability tests of the species. 相似文献
37.
As an extension of previous reports, the barium carbonate procedure has been optimized in detail for the preparation of apolar columns. The aim was to produce optimum overall column characteristics, and to maintain them unchanged under the prolonged influence of the highest possible temperature. The main parameters under optimization were glass variety, leaching of glass surface with aqueous HCl, and amount of barium carbonate deposited, while deactivation and coating were kept constant. The basic column characteristics were adsorption properties and thermostability of deactivation, acid/base behaviour and separation efficiency. They were determined by a new, quantitative testing procedure. Intense leaching was able to eliminate almost totally the differences between glass varieties and to create a well-defined glass surface. While untreated glass, leached glass, and barium carbonate treated glass showed specific weak points in the respective column quality, the combination of leaching and barium carbonate treatment yielded the highest and most stable quality. Some technical modifications of the preparation procedure are described, including deactivation in the gas phase, and use of pentane as a solvent for static coating. 相似文献
38.
Summary The feasibility of using columns prepared by mixing together ion exchange and reversed-phase packing materials, for the simultaneous separation of ionised and unionised molecules, has been examined using a range of test solutes. Columns prepared in this way showed chromatographic properties which were intermediate between those of the individual phases. The dual nature of the retention mechanism allowed the retention of ionisable molecules to be adjusted using pH whilst that of uncharged compounds was unaffected. The simultaneous chromatography of model compounds and their glucuronide, sulphate and glycine conjugates, under a variety of conditions, was demonstrated. 相似文献
39.
Summary The capabilities of sulfur hexafluoride as a mobile phase for supercritical-fluid chromatography are investigated. An evaluation
of its overall utility on the basis of separations of standard aromatic hydrocarbon odel mixtures performed on a variety of
bonded-phase, packed columns with UV detection is presented. The dependence of separation performance upon operational parameters
is also examined. A comparative evaluation of the chroamtographic properties of supercitrical sulfur hexafluoride and those
of supercritical carbon dioxide is developed from these separations under corresponding supercritical state conditions. 相似文献
40.
Summary Flexibility, strength and adsorption inertness of fused-silica capillaries permits their extensive application for the preparation
of micro-packed columns in gas chromatography. Decreasing the column diameter (from 0.5 to 0.15 mm) and the diameter of the
sorbent particles (from 100 to 5 μm) results in a marked reduction of the height equivalent to a theoretical plate (HETP),
as well as in diminishing the dependence of the HETP on the carrier gas flow rate.
The chromatographic characteristics of fused-silica capillary micro-packed columns and open-tubular columns are compared.
The fused-silica capillary micro-packed column can be used to advantage for performing rapid and trace analyses and have been
shown to be adapted for application in gas-solid chromatography. Separation of organic and inorganic compounds on fused-silica
capillary micro-packed columns is illustrated by practical examples.
Presented at the 15th International Symposium on Chromatography, Nürnberg, October 1984 相似文献