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581.
Garcia SC Schott K Charão M Moro A Bulcão R Grotto D Valentini J Bohrer D Cardoso S Pomblum V 《Biomedical chromatography : BMC》2008,22(5):460-468
Reduced glutathione (GSH) is a well-known multifunctional antioxidant. Its depletion is linked to a number of pathologies, such as renal insufficiency. Feasible methodologies in clinical chemistry are vital. Therefore a methodology for GSH quantification was optimized and validated by HPLC-UV. Important aspects such as acid deproteinization and GSH stability were established. The erythrocytes were hemolyzed, deproteinized, derivatized with 5,5-dithio-bis (2-nitrobenzoic) acid and analyzed using HPLC, on an RP18 gradient elution, lambda=330 nm. The method was applied to hemodialysis patients (n=75) compared with healthy subjects (n=40). The assay was linear from 0.5 to 3.0 mm (r2>0.99). The intra- and inter-run reproducibilities were obtained with CV%<10%. The accuracy (bias %) ranged from 1.32 to -6.38%, and the recovery was >94%. The derivatized sample was stable for 60 days at -20 degrees C. The GSH levels in hemodialysis patients showed a significant increase compared with healthy subjects (p<0.05) and an inverse correlation with age (r=-0.286; p=0.013) was found. This method used UV detection, reduction of the phosphate concentration in the mobile phase and effective protein removal with trichloroacetic acid. The method proved to be reproducible, precise, accurate and stable. Thus, it can be suggested for routine laboratory tests for the verification of physiopathological conditions. 相似文献
582.
Ruzene DS Silva DP Vicente AA Gonçalves AR Teixeira JA 《Applied biochemistry and biotechnology》2008,147(1-3):85-96
The effects of alkaline treatments of the wheat straw with sodium hydroxide were investigated. The optimal condition for extraction
of hemicelluloses was found to be with 0.50 mol/l sodium hydroxide at 55 °C for 2 h. This resulted in the release of 17.3%
of hemicellulose (% dry starting material), corresponding to the dissolution of 49.3% of the original hemicellulose. The yields
were determined by gravimetric analysis and expressed as a proportion of the starting material. Chemical composition and physico-chemical
properties of the samples of hemicelluloses were elucidated by a combination of sugar analyses, Fourier transform infrared
(FTIR), and thermal analysis. The results showed that the treatments were very effective on the extraction of hemicelluloses
from wheat straw and that the extraction intensity (expressed in terms of alkali concentration) had a great influence on the
yield and chemical features of the hemicelluloses. The FTIR analysis revealed typical signal pattern for the hemicellulosic
fraction in the 1,200–1,000 cm−1 region. Bands between 1,166 and 1,000 cm−1 are typical of xylans. 相似文献
583.
584.
585.
Paulo C. Nascimento Luciana D. Del‐Fabro Denise Bohrer Leandro M. de Carvalho Marcelo B. Rosa Simone M. Noremberg 《Electroanalysis》2008,20(10):1078-1084
Simultaneous determination of Al(III) and Fe(III) in posthemodialysis fluids was investigated by the Adsorptive stripping voltammetry of solochrome violet metal complexes. The adsorption of the complexes on the mercury electrode (HMDE) was investigated by out of phase altenating current voltammetry in presence of the main matrix interfering species. Sample digestion by UV irradiation was investigated to overcome the matrix interference. The proposed method was valid for real posthemodialysis samples containing or not Desferrioxamine B. Detection limits of 1.4 and 1.8 μg L?1 were calculated for Al(III) and Fe(III), respectively. Recoveries ranging from 88.1 to 106.3% were obtained from spiking experiments. 相似文献
586.
Leandro M. de Carvalho Paulo C. do Nascimento Denise Bohrer Raquel Stefanello Eduardo J. Pilau Marcelo B. da Rosa 《Electroanalysis》2008,20(7):776-781
This paper describes a new voltammetric procedure for the inorganic speciation of As(III) and As(V) in water samples. The procedure is based on the chemical reduction of arsenate [As(V)] to arsenite [As(III)] followed by the voltammetric determination of total arsenic as As(III) at the hanging mercury drop electrode (HMDE) by adsorptive cathodic stripping voltammetry (AdCSV) in the presence of sodium diethyl dithiocarbamate (SDDC). The reduction step involved the reaction with a mixture of Na2S2O5 and Na2S2O3 in the concentrations 2.5 and 0.5 mg mL?1, respectively, and the sample heating at 80 °C for 45 min. The linear range for the determination of total arsenic as As(III) in the presence of SDDC was between 5 and 150 μg L?1 for a deposition time of 60 s (r=0.992). A detection limit of 1.05 μg L?1 for total As was calculated for the method in water samples using a deposition time of 60 s. The detection limits of 4.2 μg L?1 and 15.0 μg L?1 for total As in seawater and dialysis concentrates, respectively, were calculated using a deposition time of 60 s. The relative standard deviations calculated were 2.5 and 4.0% for five measurements of 20 μg L?1 As(V) as As(III) in water and dialysis concentrates, respectively, after chemical reduction under optimized conditions. The method was applied for the determination of As(III) and total As in samples of dialysis water, mineral water, seawater and dialysis concentrates. Recovery values between 86.0 and 104.0% for As(III) and As(V) added to the samples prove the satisfactory accuracy and applicability of the procedure for the arsenic monitoring. 相似文献
587.
Viviane Dalmoro Jo?o H. Z. dos Santos Denise S. Azambuja 《Journal of Solid State Electrochemistry》2012,16(1):403-414
Protection from corrosion of the aluminum alloy AA2024-T3 coated with a tetraethoxysilicate (TEOS)/aminotrimethyllenephosphonic
acid (ATMP) film in a 0.05-mol L−1 NaCl solution was evaluated using electrochemical impedance spectroscopy, scanning electron microscopy, energy disperse spectroscopy,
and atomic force microscopy. The present work investigates the influence of different pretreatment procedures of the alloy
surface and the ATMP concentration on the corrosion resistance of the coated samples. The undoped sol–gel coatings did not
provide adequate corrosion protection. The best corrosion protection was achieved using acetic acid pretreatment and subsequent
deposition of an ATMP-modified TEOS film with an optimal concentration of 5.00 × 10−4 mol L−1 in the deposition bath. The acetic acid pretreatment promotes a decrease in galvanic corrosion and the surface enrichment
of aluminum favoring the metalosiloxane and the metal–phosphonic bonds with increasing likely reaction sites, thus promoting
the formation of a more homogeneous and compact coating with improved resistance. 相似文献
588.
Trantzschel T Bernarding J Plaumann M Lego D Gutmann T Ratajczyk T Dillenberger S Buntkowsky G Bargon J Bommerich U 《Physical chemistry chemical physics : PCCP》2012,14(16):5601-5604
Hyperpolarization (HP) techniques are increasingly important in magnetic resonance imaging (MRI) and spectroscopy (MRS). HP methods have the potential to overcome the fundamentally low sensitivity of magnetic resonance (MR). A breakthrough of HP-MR in life sciences and medical applications is still limited by the small number of accessible, physiologically relevant substrates. Our study presents a new approach to extend PHIP to substrates that primarily cannot be hyperpolarized due to a steady intramolecular re-arrangement, the so-called keto-enol tautomerism. To overcome this obstacle we exploited the fact that instead of the instable enol form the corresponding stable ester can be used as a precursor molecule. This strategy now enables the hydrogenation which is required to apply the standard PHIP procedure. As the final step a hydrolysis is necessary to release the hyperpolarized target molecule. Using this new approach ethanol was successfully hyperpolarized for the first time. It may therefore be assumed that the outlined multi-step procedure can be used for other keto-enol tautomerized substances thereby opening the application of PHIP to a multitude of molecules relevant to analyzing metabolic pathways. 相似文献
589.
Sliem MA Turner S Heeskens D Kalidindi SB Van Tendeloo G Muhler M Fischer RA 《Physical chemistry chemical physics : PCCP》2012,14(22):8170-8178
Stearate@Cu/ZnO nanocomposite particles with molar ratios of ZnO?∶?Cu = 2 and 5 are synthesized by reduction of the metal-organic Cu precursor [Cu{(OCH(CH(3))CH(2)N(CH(3))(2))}(2)] in the presence of stearate@ZnO nanoparticles. In the case of ZnO?∶?Cu = 5, high-angle annular dark field-scanning transmission electron microscopy (HAADF-STEM) combined with electron-energy-loss-spectroscopy (EELS) as well as attenuated total reflection Fourier transform infrared (ATR-IR) spectroscopy are used to localize the small amount of Cu deposited on the surface of 3-5 nm sized stearate@ZnO particles. For ZnO?∶?Cu = 2, the microstructure of the nanocomposites after catalytic activity testing is characterized by HAADF-STEM techniques. This reveals the construction of large Cu nanoparticles (20-50 nm) decorated by small ZnO nanoparticles (3-5 nm). The catalytic activity of both composites for the synthesis of methanol from syn gas is evaluated. 相似文献
590.
Hattori S Schmidt JA Mahler DW Danielache SO Johnson MS Yoshida N 《The journal of physical chemistry. A》2012,116(14):3521-3526
The sulfur kinetic isotope effect (KIE) in the reaction of carbonyl sulfide (OCS) with O((3)P) was studied in relative rate experiments at 298 ± 2 K and 955 ± 10 mbar. The reaction was carried out in a photochemical reactor using long path FTIR detection, and data were analyzed using a nonlinear least-squares spectral fitting procedure with line parameters from the HITRAN database. The ratio of the rate of the reaction of OC(34)S relative to OC(32)S was found to be 0.9783 ± 0.0062 ((34)ε = (-21.7 ± 6.2)‰). The KIE was also calculated using quantum chemistry and classical transition state theory; at 300 K, the isotopic fractionation was found to be (34)ε = -14.8‰. The OCS sink reaction with O((3)P) cannot explain the large fractionation in (34)S, over +73‰, indicated by remote sensing data. In addition, (34)ε in OCS photolysis and OH oxidation are not larger than 10‰, indicating that, on the basis of isotopic analysis, OCS is an acceptable source of background stratospheric sulfate aerosol. 相似文献