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961.
The new enhancement in the determination of pH using optical fiber system is described here. This work uses the membrane made of cellulose acetate membrane for reagent immobilization and congo red (pKa 3.7) and neutral red (pKa 7.2) as pH indicators. An effective covalent chemical binding procedure is used to immobilize the indicators. The response time, reversibility, linear range, reproducibility, and long-term stability of fiber optic sensor with congo red as well as neutral red have been determined. The linear range measured for the sensor based on the congo red and neutral red is 4.2-6.3 and 4.1-9.0, respectively. The response time of sensor membrane is measured by varying the substance pH values between 11.0 and 2.0. 相似文献
962.
963.
WANG Jian-ya FANG Zhao-lun . Research Center for Analytical Sciences Northeastern University Shenyang P. R. China . School of Petrochemical Engineering Shenyang University of Technology Shenyang P. R. China 《高等学校化学研究》2006,22(3):287-291
Introduction Determinationofglucoseisrequiredinmedicine industry,foodindustry,clinicaldiagnosisaswellas variousresearchfields.Therefore,intensiveefforts havebeendirectedtothedevelopmentofanalytical methodsfordeterminationofglucose,suchasthose basedonbiose… 相似文献
964.
965.
A novel application of an electrochemical biosensor is here employed as analytical method for the detection and presumptive identification of antimicrobial drug residues in milk. The measurement was based on carbon dioxide production rate in relation to inhibition of microbial grow (Escherichia coli ATCC 11303). In this pilot study quinolone and tetracycline residues have been taken into consideration because use of these last in livestock production has been identified as area of particular concern. The experimental approach and analytical method developed appear adequate for the purpose, and compared to older screening methods as, for example, the microbial inhibition assays and immunoassays, offers the advantages of (i) very short analysis time (about 120 min); (ii) smaller sample amount (approximately 0.5 mL); (iii) no sample treatment (iv) good precision; and (v) the possibility of following, in a continuous manner, the inhibition process. Moreover, sensitivity of electrochemical biosensor system is resulted very high considering that for all quinolones and tetracyclines investigated it has been possible detect a residue concentration below or equal to 25 μg L−1. Under this point of view, it must be considered that the maximum residue limits fixed by UE for quinolones and tetracyclines in milk are, at present, all higher of this concentration. 相似文献
966.
《Electroanalysis》2006,18(1):53-58
Cathodic adsorptive stripping voltammetry (AdSV) as highly sensitive and selective method for quantifying trace amounts of dissolved Ni2+‐ions has been integrated into an electrochemical robotic device using the wells of microtiter plates as low‐volume electrochemical cells. A three‐electrode assembly integrating a Bismuth film‐modified glassy carbon electrode as working electrode and a glass capillary for delivering Ni2+ standard solution in conjunction with an adapted software allowed multiple AdSV measuring cycles to be performed one after the other in the individual compartments of a 24‐well microtiter plate. Of advantage for the automation was the possibility of an in‐well electrochemical removal of used and a replating of fresh Bi films in between distinct measuring cycles. With optimized parameters for the accumulation of the complex between Ni2+‐ions and dimethylglyoxime onto the surface of the Bi film electrode and the subsequent stripping procedure, automated adsorptive stripping voltammetry in the established system offered a linear dynamic range of up to 170 nM, a sensitivity of 12 nA/nM Ni2+ and a limit of of detection of 2.1 nM (N=16) for the detection of trace levels of Ni2+‐ions. Automated AdSV certainly is of convenience for studying larger number of samples due to the high‐throughput capability of the robotic apparatus. As example, the automatic quantification of Ni2+‐ion release from electropolished surfaces of NiTi shape memory alloys during corrosion in NaCl solutions is described. 相似文献
967.
《Electroanalysis》2006,18(5):433-439
This paper presents the results of investigation on selectivity of the sulfur dioxide amperometric sensor with Nafion membrane in the presence of carbon monoxide and nitrogen dioxide as the interferents. There have been compared selectivity coefficients, for the sensors containing the following internal electrolytes: solution of sulfuric acid (concentration 5 mol dm?3) in pure water (A) and solution of sulfuric acid (concentration 5 mol dm?3) in mixed solvent dimethylsulfoxide‐water with an DMSO: H2O mole ratio of 1 : 2 (B). Values of the selectivity coefficients have been calculated based on the calibration curves. Analysis of both calibration curves and selectivity coefficients plays a significant role in optimization of a working point of a particular sensor. The investigated sensor operates in a three‐electrode system, where the working and counter electrodes are vacuum sublimation deposited on the membrane surface. 相似文献
968.
提出了一种用硅双结型色敏器件测量色温的方法.在合理的测控电路下,硅双结型色敏器件的电流对数比与实验灯泡的色温值呈良好的单值对应,经单片机处理后可以得到分段线性关系.通过对电流对数比与波长随线的数据拟合,结果表明,用硅双结型色敏器件测量色温,其测量温度可以到10^4K以上,精度可以达到10K.本文的方法与传统方法相比减少了工作量,降低了费用,具有通用性和实用价值. 相似文献
969.
YouQunCHU ChunAnMA FengMingZHAO HuiHUANG 《中国化学快报》2004,15(7):805-807
The multi-walled carbon nanotubes (MWNTs) electrode was constructed using polytetrafluoroethylene as binder, and the electrochemical reductive behavior of oxygen in alkaline solution was first examined on this electrode. Compared with other carbon materials, MWNTs show higher electrocatalytic activity, and the reversibility of O2 reduction reaction is greatly improved. The experiments reveal that the electrochemical reduction of O2 to HO2 is controlled by adsorption. The preliminary results illustrate the potential application of MWNTs in fuel cells. 相似文献
970.
The field of the rapid characterization of products by HS-MS is reviewed. The general principle of HS-MS systems consists of introducing volatile components present in the HS of a sample without prior chromatographic separation into the ionization chamber of a mass spectrometer. The spectrum resulting from simultaneous ionization and fragmentation of the mixture of molecules introduced constitutes a “fingerprint” that is characteristic of the product being analyzed. Exploitation of this spectral information allows one determine the composition of the sample. 相似文献