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631.
乳酸环丙沙星单扫描示波极谱法研究 总被引:3,自引:0,他引:3
研究了乳酸环丙沙星的极谱伏安行为,在pH=8.3的0.02mol/L,NH4Cl-NH3.H2O底液中,乳酸环丙沙星能产生1个灵敏的还原峰,峰电位为-1.61V,其导数峰高与浓度在3.9×10^-8~1.8×10^-6mol/L和1.8×10^6~1.1×10^-5mol/L范围内呈现良好的线性关系,相关系数r=0.9997,检测下限为2.5×10^-8mol/L,用于乳酸环丙沙星注射液的测定,相 相似文献
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633.
In order to visually display the migration and crystallization process of salt solution in porous cultural relics, copper sulfate solution with color rendering property was selected to record the migration, crystallization and resolution of salt solution in simulated SiO2 samples under different environmental conditions in real time through high-resolution recording system, scanning electron microscope system, salt phase X-ray diffraction system, and so on. The results showed the migration of salt solution in porous samples was related to the structural characteristics of the porous samples, the migration rate of salt solution, the evaporation rate and the change frequency of crystallization–resolution, etc., in which the large pore size of the sample, the higher the concentration and the faster migration and evaporation rate of salt solution, the greater the change rate of the brine accumulation zone or salt crystallization zone in the different porous samples. During the humidification–drying cycles of rainfall, the higher the cycle frequency of humidification–drying was, the higher the drying temperature was, the more frequent the crystallization-analysis change of salt in the salt-bearing sample was, and the more extensive the distribution of salt crystal zone was. This is the first time to visualize the salt belt by simulating the changing process of a salt solution with a color rendering property in porous samples. This has scientific theoretical guidance for the study of the migration–crystallization changes of soluble salts contained in porous silicate cultural relics. The visibility analysis results of multilayer salt crystal belts can also provide the preliminary basis for further effective desalination of salt bearing cultural relics. 相似文献
634.
Square-wave adsorptive stripping voltammetry technique was used to determine rosiglitazone (ROS) on the hanging mercury dropping electrode (HMDE) surface, in Britton Robinson buffer, pH = 5. The voltammetric cathodic peak was observed at ?1520 mV vs. Ag/AgCl reference electrode. The voltammetric peak response was characterized with respect to pH, supporting electrolyte, accumulation potential, preconcentration time, scan rate, frequency, pulse amplitude, surface area of the working electrode and the convection rate. Under optimal conditions, the voltammetric current is proportional to the concentration of ROS over the concentration range of 5 × 10?8–8 × 10?7 mol l?1 (r = 0.9899) with a detection limit of 3.2 × 10?11 mol l?1 using 120 s accumulation time. The developed SW-AdSV procedure showed a good reproducibility, the relative standard deviation RSD% (n = 10) at a concentration level of 5 × 10?7 mol l?1 was 0.33%, whereas the accuracy was 101% ± 1.0. The proposed method was successfully applied to assay the drug in the human urine and plasma samples with mean recoveries of 90 ± 0.71% and 86 ± 1.0%, respectively. 相似文献
635.
《Analytical letters》2012,45(13):1519-1531
Abstract The application of adsorptive stripping analysis in combination with differential pulse voltammetry for the determination of some triazine- and nitro group- containing pesticides like Dinobutone, DNOK, Ametryne and Prometryne is described. Conditions for determinations in the concentration range from approx. 0.1 to 50 ppb are given. 相似文献
636.
Four new oxazoline based macrocycles have been constructed, said cycles were found to possess varying cytotoxicity against six different cancer cell lines: IC50 values of 6.4 μM towards HeLa and 11.9 μM towards LnCaP being the most potent. Two of the four macrocycles were found to have marginal cytotoxicity against MM.1S and MM.1R, myeloma cancer cell lines, and further evaluation showed that they also possessed rapid cellular uptake and accumulation characteristics. Through the structure-activity relationship comparisons between the four compounds, it was found that the C6 position of the E-ring is amendable to substitution and could possibly serve as a conjugation site for the development of a selective delivery system to MM.1R. 相似文献
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在0.01mol/LKOH底液中(pH=11.7),用单扫示波极谱法可获得钙-芦丁络合吸附波,检出限为8.0×10-7mol/L.测得电活性络合物组成为Ca(Ⅱ)∶Rt=1∶2,条件稳定常数为β=4.8×1010.电极表面反应速率常数为ks=1.27s-1. 相似文献
640.
在pH9.3的Na2B4O7Na2CO3缓冲溶液中,铬(Ⅵ)与十六烷基三甲基溴化铵(CTMAB)在滴汞电极上吸附还原,峰电位-0.31V(vs.SCE).铬(Ⅵ)在1.9×10-82.1×10-6mol/L范围内与峰高呈线性关系检出限为77×10-9mol/L用于工业废水中铬的测定,结果与光度法一致 相似文献