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931.
A. S. Bansode Siddharth Patel T. Rajesh Kumar B. Muralidhar T. Sundararajan Sarit Kumar Das 《Heat and Mass Transfer》2007,43(10):1037-1047
A 3D numerical study was carried out to analyze flow, heat and mass transfer first in a single half-cell cathode channel of
proton exchange membrane (PEM) fuel cell. From practical point of view, it is necessary to put the appropriate number of cells
in a stack. Hence, the above study on a single half-cell is extended to a stack of channels. Due to stacking, the assumption
of uniform flow distribution would no longer hold true. Therefore, the channel flow-maldistribution is considered. The water
formed at the active surface due to the electrochemical reaction diffuses through the porous layer and eventually enters the
gas flow duct. The higher gas velocities in the duct result in faster water vapour removal which leads to a lower value of
water vapour into the duct and hence a lower Nusselt number. 相似文献
932.
Direct Determination of Trace Dopamine in an Ascorbic Acid Solution at a Bare Glassy Carbon Electrode Using Differential Pulse Voltammetry
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Lijian Sun Jing Chen Fangmin Zhao Na Liu Yingqiu Zhang Jianbo Jia Jianguo Wang 《Electroanalysis》2015,27(6):1411-1415
It is difficult to monitor dopamine (DA) accurately with a bare glassy carbon electrode because of the interference of ascorbic acid (AA). In this paper, a method for the determination of DA in an AA solution using differential pulse voltammetry was established. Because AA loses its electrochemical activity after being oxidized, hydrogen peroxide was used to oxidize AA, and the interference of AA was completely eliminated. As a result, trace DA could be directly determined in the AA solution with a bare glassy carbon electrode. When trace DA was determined in a 1.0 mmol L?1 AA solution, there was a wide linear range from 3.0×10?8 mol L?1 to 1.0×10?5 mol L?1. The application of this method was demonstrated by the selective measurement of DA in an injection without pretreatment. 相似文献
933.
A Nitrite Electrochemical Sensor Based on Boron‐Doped Diamond Planar Electrochemical Microcells Modified with a Monolacunary Silicotungstate Polyoxoanion
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Yosra Sahraoui Amel Sbartai Sana Chaliaa Abderrazak Maaref Amor Haddad Nicole Jaffrezic‐Renault 《Electroanalysis》2015,27(6):1359-1367
A new boron doped diamond microcells (BDD) was modified, for rapid, selective and highly sensitive determination of nitrite, using a coating film of polyoxometalates (POMs), formed by cyclic voltammetry on the molecular p‐phenylenediamine (PPD) functionalized BDD. The scanning electron microscopy (SEM) technique was used to examine the morphology of (PPD/SiW11) modified (BDD) electrode. It was found that (SiW11) layer was uniformly formed on the electrode surface. It was observed that (BDD/PPD/SiW11) showed excellent electrocatalytic activities towards nitrite ion. Under the selected conditions, the anodic peak maximum at ?0.6 V was linear versus nitrite concentration in the 40 µM–4 mM range, and the detection limit obtained was 20 µM. The newly developed electrode has been successfully applied to the determination of nitrite content in real river water samples. 相似文献
934.
Electroanalytical Studies of Chromone Based Ionophores for the Selective Determination of Arsenite Ion
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Neha Gupta Ashok Kumar Singh Shubhrajyotsna Bhardwaj Divya Singhal 《Electroanalysis》2015,27(5):1166-1175
Two chemosensors 4H‐1‐benzopyran‐3‐carboxaldehyde, 4‐oxo‐, 3‐(2‐phenylhydrazone), [I1] and 4H‐1‐benzopyran‐3‐carboxaldehyde, 4‐oxo‐, 3‐[2‐(2,4‐dinitrophenyl)hydrazone], [I2] with hydrazone‐NH group as binding site have been shown excellent selectivity for arsenite ion. It is confirmed by the UV‐vis titration that I2 is more selective than I1. The performance of the coated graphite electrode (CGE) was found to be better than polymeric membrane electrode (PME) in terms of linear range of 4.89×10?7–1.0×10?1 mol L?1, low detection limit of 8.31×10?8 mol L?1 and short response time. The proposed sensors were also used to determine the arsenite ion in different water samples. 相似文献
935.
Franck Charmantray Nadia Touisni Laurence Hecquet Thierry Noguer Christine Mousty 《Electroanalysis》2015,27(6):1341-1344
This paper describes the development of an amperometric biosensor based on galactose oxidase (GAOx) immobilization within a laponite clay film deposited on Carbon Screen‐Printed Electrodes modified by electrodeposited Prussian Blue and coated with poly‐(O‐phenylenediamine) (PPD/PB/CSPEs). Amperometric performances of GAOx@laponite/PPD/PB/CSPEs bioelectrodes were determined using several GAOx substrates. Using these modified electrodes the reduction of enzymatically generated hydrogen peroxide was performed at ?0.2 V vs. Ag‐AgCl. In an initial attempt, E.Coli transketolase activity on its immobilized form was followed using a bienzymatic GAOx‐TK biosensor. 相似文献
936.
Simple,Rapid and Sensitive Electrochemical Method for the Determination of the Triketone Herbicide Sulcotrione in River Water Using a Glassy Carbon Electrode
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We report a novel, simple, rapid and sensitive electrochemical method for the determination of sulcotrione, a member of the relatively new class of triketone herbicides, using differential pulse voltammetry on a glassy carbon electrode. Its electrochemical behavior including influences of electrolyte composition, pH and scan rate was studied to select optimal experimental parameters for its determination. In Britton? Robinson buffer at pH 3 sulcotrione provided a well‐defined reduction peak at ?0.84 V (vs. Ag/AgCl electrode), with good repeatability (relative standard deviation of 2.3 % for 8 measurements at 10 µM concentration level). With optimized parameters differential pulse voltammetry rendered two linear concentration ranges from 0.2 to 2 µM and from 2 to 50 µM with a detection limit of 0.05 µM. The proposed procedure was successfully applied to the determination of sulcotrione in spiked river water samples with satisfactory recoveries (93–109 %). The developed method may represent a simple, rapid and sensitive alternative to highly toxic mercury electrodes and chromatographic methods. 相似文献
937.
Electrochemical Activity of Wedelolactone and Probing its Interaction with DNA Using Voltammetry at a Carbon Electrode
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Wedelolactone (WLA) is a polyphenolic coumestan derivative found in extracts of plants used in traditional medicine. Due to its cytostatic activity, WLA is one of natural compounds tested as potential anticancer drugs. In this work we for the first time studied electrochemical properties of WLA using cyclic (CV) and square‐wave (SWV) voltammetry at the basal‐plane pyrolytic graphite electrode. A reversible pair of peaks, corresponding to catechol/o‐benzoquinone redox system, was observed using CV around 0.275 V vs. Ag|AgCl|3 M KCl reference electrode. Measurements of SWV signal of WLA in the presence of single‐ or double‐stranded DNA suggested a weak interaction without evident preference for double‐stranded DNA. An indirect assay, employing electroactive DNA intercalator doxorubicin as competitor, confirmed absence of intercalative DNA binding of WLA. 相似文献
938.
Determination of Allura Red and Tartrazine in Food Samples by Sequential Injection Analysis Combined with Voltammetric Detection at Antimony Film Electrode
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J. A. Rodríguez M. G. Juárez C. A. Galán‐Vidal J. M. Miranda E. Barrado 《Electroanalysis》2015,27(10):2329-2334
An antimony film electrode prepared on‐line and installed as part of a sequential injection system, was used as an electrochemical detector to determine azo dyes in food samples. The influence of several flow variables were evaluated using a central composite design. In optimal conditions, the linear range of the calibration curve varied from 1–5 µM, with a limit of detection limit of 0.3 µM. The relative standard deviation of analytical repeatability was <5.0 %.The method was validated by comparing the results obtained with those provided by HPLC; no significant difference were seen. 相似文献
939.
Amperometric Folic Acid Quantification Using a Supramolecular Tetraruthenated Nickel Porphyrin µ‐Peroxo‐Bridged Matrix Modified Electrode Associated to Batch Injection Analysis
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Luís M. C. Ferreira Paulo R. Martins Koiti Araki Henrique H. Toma Lúcio Angnes 《Electroanalysis》2015,27(10):2322-2328
A supramolecular Nickel (II) porphyrin complex containing four pyridyl‐bis(2,2′‐bipyridyl)chloro ruthenium meso substituents was submitted to successive voltammetric cycles in high alkaline media to produce a supramolecular matrix with Nickel centers linked by µ‐peroxo bridges, producing a highly stable thin film able to act as redox mediator for electrocatalytic oxidation of folic acid. The characterization of electrode surface material was performed by Scanning Electron Microscopy and Electrochemical Impedance Spectroscopy. The modified electrode was inserted into a batch injection electrochemical cell used for the rapid and precise quantification of folic acid in pharmaceutical products. The favorable hydrodynamic conditions provided by amperometry‐BIA association allowed a very high throughput with good linear range (1 to 200 µmol L?1) and low detection limit (7.37×10?7 mol L?1). The electrochemical method was applied to the quantification of folic acid in different tablet samples. The results were comparable with values indicated by the manufacturer and those found using high HPLC according to the Brazilian Pharmacopoeia; commercial samples were submitted to a procedure in order to remove lactose of tablets, since carbohydrates act as interfering species. This procedure together with the electrochemical method showed to be simple, rapid, efficient and an appropriate alternative for quantifying this compound in real samples. 相似文献
940.
Construction of a Novel Carbon Paste Clarithromycin Sensor for Low Level Concentration Measurement,Applications to Pharmaceutical and Biological Analysis
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A potentiometric carbon paste sensor was fabricated for determination of clarithromycin based on incorporation of the ion association complex of the clarithromycin‐phosphotungstate. The proposed sensor exhibited a Nernstian slope of 59.2±0.3 mV per decade for clarithromycin over a wide concentration range of 7.4×10?7 to 1.5×10?3 M, with a low detection limit of 5.0×10?7 M. The proposed sensor manifested advantages of very fast response, long life time and, most importantly, excellent selectivity for clarithromycin relative to a wide variety of common foreign inorganic cation, and also biological species. The sensor was successfully applied to determine clarithromycin in clarithromycin tablet, blood serum and urine samples. The inclusion complex formation between β‐cyclodextrin and clarithromycin was studied by the proposed sensor. The influence of the temperature on the response of the sensor was investigated and the temperature coefficient of the sensor was calculated. 相似文献