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21.
A method is described for neutron activation analysis of thorium by employing thorium-233. Decontamination steps include anion exchange in 12.5 N HCL, precipitation of fluoride, extraction with mesityl oxide and thorium oxalate precipitation. The time spent is less than 1 h; spurious activities in counting samples amount only to 2% and can easily be corrected for. The sensitivity of the method is ca. 0.02 μg of thorium in a neutron flux of 1012n/cm2/sec with an irradiation time of 5 min. 相似文献
22.
Abramova N Borisov Y Bratov A Gavrilenko P Domínguez C Spiridonov V Suglobova E 《Talanta》2000,52(3):533-538
Application of a potassium ion sensor based on an ion sensitive field effect transistor (ISFET) for ion control of a dialysis solution in an artificial kidney and in blood plasma of patients treated by hemodialysis is presented. Sensors and their long-term stability were characterised in constant contact with test solutions. Test results are compared to those obtained with conventional ion-selective electrodes and commercial blood ion analyser. Tested ISFET sensors showed high reliability in potassium ion measurements in the physiologically significant concentration range which, along with low cost of their production, makes them promising for cited application. 相似文献
23.
Carabias-Martínez R Rodríguez-Gonzalo E Revilla-Ruiz P Domínguez-Alvarez J 《Journal of chromatography. A》2003,990(1-2):291-302
Micellar electrokinetic capillary chromatography (MEKC) with diode array detection was used for the separation of 13 compounds (eight herbicides widely used in agriculture: metribuzin, lenacil, ethofumesate, atrazine, terbutryn, isoproturon, chlorotoluron and linuron, and five of their principal degradation products; namely, deethylatrazine, 2-hydroxyatrazine, deethyl-2-hydroxyatrazine, deisopropylatrazine and 3-chloro-4-methylphenylurea). Peak separation for the 13 analytes was not successful when a single surfactant system was employed, neither sodium dodecyl sulfate (SDS) nor dioctyl sulfosuccinate (DOSS) sodium salt. However, a mixture of these herbicides was successfully separated using a mixed micellar system involving SDS–DOSS in less than 14 min. An application study of an on-line concentration technique for MEKC was carried out to enhance sensitivity. The optimized on-line stacking procedure consisted simply of the addition of 50 mM of sodium chloride to the injection sample, the stacking effect being more intensive as analyte polarity increased. When this stacking procedure was combined with an off-line sample preconcentration step, based on solid-phase extraction, analytes could be detected in the ppb range. The whole method was applied to ultra-high-quality and natural waters. Linear relationships between the analytical signal and the initial analyte concentration were found to be independent of the type of water, except for the more polar analytes for which small differences were observed. 相似文献
24.
The complete assignment of the proton chemical shifts of coumarin ( 1 ), all monomethoxy derivatives and the six possible dimethoxyl substituted compounds at the aromatic ring was achieved at 60 MHz in a quantitative study utilizing Pr(fod)3 as the shift reagent. It was found that in addition to the complexation at the lactone carbonyl a second interaction of the lanthanide shift reagent occurs when two methoxyl groups are found in an ortho distribution. The results are discussed in comparison to data published for flavones in the presence of Pr(fod)3 shift reagent. 相似文献
25.
The electrical conductivities of sodium chloride and sodium iodide solutions in formamide-water mixtures of different composition have been measured at 25°C. From these data, the limiting equivalent conductances for these salts have been determined. The correspondingWalden products are compared together with the one reported for sodium bromide in the same solvent mixtures, and they are analysed as functions of the anion size. Further, the limiting ionic equivalent conductances are estimated for the different ions. The variation of the ionicWalden products with solvent composition is discussed in terms of ionic solvation and solvent structure.
Elektrische Leitfähigkeit von Halogensalzen in wäßrigen Formamid-Lösungen
Zusammenfassung Es wurden die elektrischen Leitfähigkeiten von Natriumchlorid- und Natriumjodidlösungen in Formamid-Wasser-Mischungen verschiedener Zusammensetzung bei 25°C gemessen. Aus diesen Daten wurden die Grenzäquivalenzleitfähigkeiten für diese Salze bestimmt. Die entsprechendenWalden-Produkte wurden mit den für Natriumbromid in den gleichen Lösungsmittelgemischen berichteten verglichen und hinsichtlich der Anionengrößen analysiert. Außerdem wurden die ionischen Grenzäquivalenzleitfähigkeiten für die einzelnen Ionen abgeschätzt. Die Variation der ionischenWalden-Produkte mit der Lösungsmittelzusammensetzung wurde bezüglich Ionensolvatation und Lösungsmittelstruktur diskutiert.相似文献
26.
Optimisation of stir bar sorptive extraction for the analysis of volatile phenols in wines 总被引:2,自引:0,他引:2
An easy, fast and reliable analytical method is proposed for the determination of the concentration of volatile phenols (ethyl- and vinylphenols) in wines. The novel stir bar sorptive extraction (SBSE) technique is employed, following a simple and fast procedure that allows 15 samples to be extracted simultaneously using very small sample volume. Extracts are desorbed in a thermodesorption system (TDS) coupled on-line to a gas chromatograph-mass spectrometry system. The SBSE offers better recovery and linear regression coefficient (r2) for the four volatile phenols than solid-phase extraction (SPE). The mass spectrometric detection in selected ion monitoring mode contributes to the lower detection limit and good sensibility obtained with this method. 相似文献
27.
The electrochemistry of monoclinic and tetragonal vanadium-doped zirconias (VZrO2), prepared from gel precursors with vanadium loadings ranging from 0.5 to 15 mol%, has been studied using abrasive-conditioned
graphite/polyester composite electrodes immersed in aqueous HCl and HClO4 solutions. Isolated vanadium centers form a solid solution in the zirconia lattice with a solubility limit close to 5 mol%.
Above 5 mol%, finely dispersed V2O5 is formed. Vanadium centers located at the boundary sites of the zirconia lattice display successive one-electron transfer
processes near to +0.25 and +0.10 V vs. SCE, whereas finely dispersed V2O5 yields three successive reduction processes at +0.46, +0.30, and +0.16 V vs. SCE. Electrochemical data indicate the presence
of both V5+ and V4+ centers in the lattice of monoclinic and tetragonal zirconias, the V5+/V4+ ratio decreasing as the vanadium loading increases.
Electronic Publication 相似文献
28.
Carabias-Martínez R Rodríguez-Gonzalo E Domínguez-Alvarez J García Pinto C Hernández-Méndez J 《Journal of chromatography. A》2003,1005(1-2):23-34
A preconcentration study based on the cloud point phenomenon was carried out for a set of triazine herbicides, three of them chloro-substituted and three of them methylthio-substituted. Concentration factors and recoveries were calculated as function of the percentage of the non-ionic surfactant Triton X-114 employed. From these values, obtained from a cloud point extraction (CPE) procedure, the distribution coefficient between the Triton X-114 micelles and water, Kc, prior to CPE was calculated for each triazine and related to the corresponding octanol-water partition coefficient, Kow. In order to confirm the results obtained with the triazine herbicides, two sets of data from chemically different organic pollutants--organophosporous and chlorophenols--obtained from the literature were assessed, concluding that they display a similar behaviour to that of the triazine herbicides. This can be used to predict the CPE behaviour of other organic pollutants from their octanol-water partition coefficients. The Kc values were compared with the analyte concentration ratio in the surfactant-rich phase and aqueous phase (Ksa) with a view to obtaining a link between the analyte behaviour prior to and after cloud point extraction procedures. 相似文献
29.
Carabias-Martínez R Rodríguez-Gonzalo E Domínguez-Alvárez J Hernández-Méndez J 《Electrophoresis》2002,23(3):494-501
The separation and determination of a mixture of chloro- and methylthiotriazines in water samples by both micellar electrokinetic capillary chromatography (MEKC) and nonaqueous capillary zone electrophoresis (NA-CZE) were compared. The characteristics of both methods proved to be very similar in terms of separation efficiency and analysis times, but application of these methods for the analysis of triazines in natural waters, with a prior preconcentration step, revealed significant differences. A preconcentration step by solid-phase extraction (SPE) with Oasis HLB cartridges was accomplished for the determination of triazines at sub-ppb levels in drinking and river waters; when NA-CZE was used after this SPE step, electropherograms with fewer interferences and more stable baselines were obtained than when separation was carried out using MEKC. Another aspect related to the application to real samples was the lack of precision encountered upon evaluating the electrophoretic signals generated when using SPE coupled with NA-CZE. Here, we demonstrate the importance of choosing an appropriate internal standard for analyte quantification. It is recommended that a triazine belonging to the same family as that of the triazine to be determined should be used as internal standard. 相似文献
30.
A procedure based on the technique of the pyrolysis-gas chromatography-mass spectrometry (Py-GC-MS) has been applied, in this work, in order to determine the composition of diterpenoid resin employed in art works. The method is based on the on line derivatization of these resins using hexamethyldisilazane (HMDS). Results obtained were compared with those previously reported in literature from Venice turpentine, Strasbourg turpentine, colophony, sandarac and Manila copal using this same method and with those others from in situ thermally assisted hydrolysis and methylation with tetramethylammonium hydroxide (TMAH). Canada balsam, copper resinate and Copaiba balsam have been also analyzed extending the scope of this method in the field of the analysis of artwork materials. Several non-reported trimethylsilylated derivatives of compounds present in the diterpenoid resins have been identified. An improvement in sensitivity has been obtained by using HMDS as derivatizing reagent, together with a better resolution of the most representative peaks. Additionally, this method reduces the number of pyrolytic fragmentation, recombination, dehydration and isomerization products formed during the pyrolysis process and, in consequence, more simplified chromatograms are obtained. Finally, the reported procedure has been successfully used for characterizing two diterpenoid resin-based varnishes present in the canvas painting "The Betrothal of the Virgin" (Anonymous, 17th century) which is included in the pictorial collection of Saint Joseph Church in Taormina (Italy) and the Magdalena Tryptich (Master of Alzira, 16th century, Valencia, Spain). 相似文献