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71.
H.-D. Pfannes D. S. Vieira Junior R. Paniago J. H. Dias Filho 《Hyperfine Interactions》2005,165(1-4):247-252
The formation of local moments and the effect of charge carrriers in dilute magnetic semiconductors can be well understood using local probe techniques like Mossbauer Spectroscopy. We report here on Mossbauer studies in the systems Fe0.008Ge1 ? x D x (D = As, Bi), Fe0.008Ge1 ? x In x , and Fe0.008Ge1 ? x Sn x . At room temperature magnetic interactions were observed for donor (D) impurities at the Fe site in the Fe0.008Ge system. No such magnetic ordering was observed for acceptor (In) or neutral (Sn) impurities. 相似文献
72.
73.
H. L. Seifert J. M. Wouters D. J. Vieira H. Wollnik X. G. Zhou X. L. Tu Z. Y. Zhou G. W. Butler 《Zeitschrift für Physik A Hadrons and Nuclei》1994,349(1):25-32
The ground state masses of thirty-nine neutronrich nuclei from51Ca to72Ni have been measured using the Time-of-Flight Isochronous (TOFI) spectrometer. Eight of these masses have been measured for the first time and thirty-one are remeasurements of neutron-rich nuclei previously reported. Good agreement between these results and a previous TOFI experiment was observed except for the most neutron-rich isotopes of vanadium through iron with the present results being more bound and in better agreement with theory. The low binding energy of68Ni, as indicated by an unreasonably low two-neutron separation energy, suggests the presence of a high-lying, long-lived isomeric state in this nucleus. 相似文献
74.
A new methodology for the determination of the fluorescence quantum yield of dyes adsorbed onto microcrystalline cellulose is presented and applied to rhodamine 101, cresyl violet and auramine O. It is based on a previously reported method by Ruetten and Thomas (J. Phys. Chem., 1998, 102, 598-606), which is not applicable to the dyes used in the present study. It uses ground-state diffuse reflectance spectra obtained with and without filters, which prevents the luminescence of the dye from reaching the integrating sphere and the photodetector. New equations are presented here, correcting for the fluorescence emission of the dye, which depends on the detector sensitivity. Cut-on filters, which have a transmittance close to unity in the absorption region, and close to zero in the emission region, of the dye are used to obtain corrected reflectance spectra. The influence of the substrate was also taken into account. This methodology may be applied to other probes and surfaces or emissions of a different nature (i.e., phosphorescence or delayed fluorescence), and constitutes a very simple and general procedure to solve the important problem of luminescence quantum yield determination of probes adsorbed onto solid powdered surfaces. 相似文献
75.
J. L. C. Diniz R. D. Vieira J. T. Castro A. C. Benjamin J. L. F. Freire 《Experimental Mechanics》2006,46(6):765-775
This paper presents the analysis of stress and strain data acquired with the finite element method and with tests that used
post-yielding strain gages bonded onto the external surface of pipes that suffered thickness metal loss and that had been
loaded with internal pressure. These metal loss areas were produced by three different processes: actual internal corrosion,
careful machining of external patches by spark-erosion, and milling of internal or external patches to simulate limited or
extensive strip corrosion defects with depths up to 70% of the pipe’s thickness. Results show that: (1) the extensive longitudinal
internal or external defect areas behave as extensive strips with a high degree of freedom to deform elastically and plastically
in the circumferential and thickness directions, and (2) large restraints are offered to the longitudinal strains by the non-corroded
thick walls parallel to the strip. Using the above experimental observation, a simple mathematical model was developed to
predict the burst pressure of pipes with longitudinal extensive and reasonably constant depths of metal loss. This model employed
thin-pipe-strength-of-material equations associated to a bulging correction factor, the material’s uniaxial ultimate strength
and the von Mises criterion. The onset of plastic collapse predicted by the simple model was successfully compared with results
determined from actual hydrostatic tests that were carried out with full scale pipe specimens and from finite element results
generated by the use of a commercial program. The developed model was also helpful in showing that the yield and burst behaviors
of new or corroded pipeline specimens under laboratory test conditions can be directly compared and extended to the yield
and burst behaviors of buried pipeline in field operation. 相似文献
76.
Quantitation of sunitinib,an oral multitarget tyrosine kinase inhibitor,and its metabolite in urine samples by nonaqueous capillary electrophoresis time of flight mass spectrometry 下载免费PDF全文
Juana Rodríguez Gregorio Castañeda Lorena Muñoz Jose C. Villa 《Electrophoresis》2015,36(14):1580-1587
A rapid, sensitive, and specific method was developed and validated using a nonaqueous‐capillary electrophoresis method with TOF‐MS for determination of sunitinib and N‐desethyl sunitinib in human urine. In order to avoid ionic suppression a urine samples dilution with methanol 1:10 previous step was used. This was the only treatment step to urine samples before the injection. Despite this dilution of the urine, the detection limit was as low as 0.07 mg/L for sunitinib and 0.15 mg/L for N‐desethyl sunitinib. Separation of compounds was achieved with a mixture of 5 mM ammonium formate in methanol. The calibration curves were linear over the range of 0.5–50.0 mg/L for the two analyzed compounds. The within‐run and between‐run precisions were within 5%, while the accuracy ranged from 96.0 to 100.4%. This method can be used in routine clinical practice to monitor sunitinib and N‐desethyl sunitinib drugs in the urine of cancer patients treated with once daily administration. 相似文献
77.
Vivian E. Cornelio Mariele M. Pedroso André S. Afonso João B. Fernandes M.Fátima G.F. da Silva Ronaldo C. Faria Paulo C. Vieira 《Analytica chimica acta》2015
The hemoglobin (Hb) released from erythrocytes is a primary nutritive component for many blood-feeding parasites. The aspartic protease cathepsin D is a hemoglobinase that is involved in the Hb degradation process and is considered an interesting target for chemotherapy intervention. However, traditional enzymatic assays for studying Hb degradation utilize spectrophotometric techniques, which do not allow real-time monitoring and can present serious interference problems. Herein, we describe a biosensor using simple approach for the real-time monitoring of Hb hydrolysis as well as an efficient screening method for natural products as enzymatic inhibitors using a quartz crystal microbalance (QCM) technique. Hemoglobin was anchored on the quartz crystal surface using mixed self-assembled monolayers. The addition of the enzyme caused a mass change (frequency shift) due to Hb hydrolysis, which was monitored in real time. From the frequency change patterns of the Hb-functionalized QCM, we evaluated the enzymatic reaction by determining the kinetic parameters of product formation (kcat). The QCM enzymatic assay using immobilized human Hb was shown to be an excellent approach for screening possible inhibitors in complex mixtures, opening up a new avenue for the discovery of novel inhibitors. 相似文献
78.
A Novel Alkaloid from Aspidosperma pyricollum (Apocynaceae) and Complete 1H and 13C Chemical Shift Assignments 下载免费PDF全文
Hádria M. do Carmo Raimundo Braz‐Filho Ivo J. Curcino Vieira 《Helvetica chimica acta》2015,98(10):1381-1386
A novel natural product indole, alkaloid, named rel‐pyricolluminol ( 1 ), was isolated from Aspidosperma pyricollum Müll .Arg . together with six known metabolites sitsirikine ( 2 ), aparicin ( 3 ), ulein ( 4 ), stemmadenine ( 5 ), lupeol ( 6 ), and (3β)‐sitoster‐3‐yl β‐D ‐glucopyranoside ( 7 ). These compounds were characterized on the basis of their spectral data, mainly 1D‐ (1H,13C‐DEPTQ) and 2D‐NMR (1H,1H‐COSY, NOESY, HSQC, and HMBC), and mass spectra (EI‐MS and HR‐ES‐MS), involving also comparison with data from the literature. 相似文献
79.
João M. Leça Ana C. Pereira Ana C. Vieira Marco S. Reis José C. Marques 《Analytica chimica acta》2015
Vicinal diketones, namely diacetyl (DC) and pentanedione (PN), are compounds naturally found in beer that play a key role in the definition of its aroma. In lager beer, they are responsible for off-flavors (buttery flavor) and therefore their presence and quantification is of paramount importance to beer producers. Aiming at developing an accurate quantitative monitoring scheme to follow these off-flavor compounds during beer production and in the final product, the head space solid-phase microextraction (HS-SPME) analytical procedure was tuned through experiments planned in an optimal way and the final settings were fully validated. Optimal design of experiments (O-DOE) is a computational, statistically-oriented approach for designing experiences that are most informative according to a well-defined criterion. This methodology was applied for HS-SPME optimization, leading to the following optimal extraction conditions for the quantification of VDK: use a CAR/PDMS fiber, 5 ml of samples in 20 ml vial, 5 min of pre-incubation time followed by 25 min of extraction at 30 °C, with agitation. The validation of the final analytical methodology was performed using a matrix-matched calibration, in order to minimize matrix effects. The following key features were obtained: linearity (R2 > 0.999, both for diacetyl and 2,3-pentanedione), high sensitivity (LOD of 0.92 μg L−1 and 2.80 μg L−1, and LOQ of 3.30 μg L−1 and 10.01 μg L−1, for diacetyl and 2,3-pentanedione, respectively), recoveries of approximately 100% and suitable precision (repeatability and reproducibility lower than 3% and 7.5%, respectively). The applicability of the methodology was fully confirmed through an independent analysis of several beer samples, with analyte concentrations ranging from 4 to 200 g L−1. 相似文献
80.
Gabriela Furlan Giordano Luis Carlos Silveira Vieira Angelo Luiz Gobbi Renato Sousa Lima Lauro Tatsuo Kubota 《Analytica chimica acta》2015
An integrated platform was developed for point-of-use determination of ethanol in sugar cane fermentation broths. Such analysis is important because ethanol reduces its fuel production efficiency by altering the alcoholic fermentation step when in excess. The custom-designed platform integrates gas diffusion separation with voltammetric detection in a single analysis module. The detector relied on a Ni(OH)2-modified electrode. It was stabilized by uniformly depositing cobalt and cadmium hydroxides as shown by XPS measurements. Such tests were in accordance with the hypothesis related to stabilization of the Ni(OH)2 structure by insertion of Co2+ and Cd2+ ions in this structure. The separation step, in turn, was based on a hydrophobic PTFE membrane, which separates the sample from receptor solution (electrolyte) where the electrodes were placed. Parameters of limit of detection and analytical sensitivity were estimated to be 0.2% v/v and 2.90 μA % (v/v)−1, respectively. Samples of fermentation broth were analyzed by both standard addition method and direct interpolation in saline medium based-analytical curve. In this case, the saline solution exhibited ionic strength similar to those of the samples intended to surpass the tonometry colligative effect of the samples over analyte concentration data by attributing the reduction in quantity of diffused ethanol vapor majorly to the electrolyte. The approach of analytical curve provided rapid, simple and accurate analysis, thus contributing for deployment of point-of-use technologies. All of the results were accurate with respect to those obtained by FTIR method at 95% confidence level. 相似文献