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981.
《Analytica chimica acta》2003,477(2):315-324
This paper describes a method for the determination of lysine based on a flow injection (FI) differential potentiometry system. The flow injection manifold is composed of a support electrolyte solution channel and a water channel acting as a carrier into which the sample solution is injected. The lysine biosensor was consisted of lysine oxidase chemically immobilized on a nylon membrane and attached to an all-solid-state ammonium electrode. A circular ammonium electrode was used as a reference. Hence, the possible interference of endogenous ammonium can be partly corrected by differential potentiometry. In order to increase the sensitivity of the response, the reaction was kinetically developed following a stopped-flow method. As a result, the sensitivity increased from 20 to 40 mV per decade when comparing the FI and the stopped-flow values. Furthermore, the peak-to-peak stopped-flow signals generated can be used as a more selective analytical response for lysine. The quantification of lysine in mixture samples containing small amounts of ammonium can be achieved with an acceptable accuracy, with prediction errors lower than 4%. However, when the ammonium concentration exceeded the lysine concentration, multivariate calibration with non-linear partial least squares (PLS) regression was needed to improve the lysine quantification, with an overall prediction error around 10%. 相似文献
982.
Subnanogram detection of steroids has become increasingly important today. One applicable method for gas chromatographic determination of subnanogram quantities of estrogens as halogenated derivatives is electron capture detection. HFB-derivatives of 7 different estrogens were automatically injected onto a prolonged narrow bore wall-coated glass capillary column. Normal split injection could not be used for this trace analysis because of too much loss of sample. Only small amounts of sample were available from which double analysis had to be performed. Cross-contamination of the automatic sampling system as well as precision of retention times and peak areas were determined. The type of injection described showed better quantitative results compared to the splitless injection technique. All details of the system used together with the results are this discussed in this paper. 相似文献
983.
催化动力学流动注射荧光光度法测定微量亚硝酸根 总被引:6,自引:0,他引:6
基于亚硝酸根离子在硫酸介质中催化溴酸钾氧化罗央明6G使其荧光强度降低的反应,建立了快速,灵敏,简便的催化动力学流动注射荧光光度法测定亚硝酸根的新方法。 相似文献
984.
直接荧光法和流动注射荧光法测定微量磷的研究 总被引:4,自引:0,他引:4
建立了利用罗丹明6G-磷钼杂多酸离子缔合物测定微量磷的直接荧光法和流动注射荧光法,最大激发光波长350nm,最大发射光波长555nm,流动注射荧光法保持直接荧光法灵敏度高、选择性好的优点,同时使测定更加简便、快速,用于测定铜合金、钢样、锰矿中微量磷获得满意结果。 相似文献
985.
A novel organic reagent 3-(8-quinolinylazo)-4-hydroxybenzoic acid (QAHBA) was synthesized for chemically modified nanometer-sized alumina, and it was characterized with infrared spectrum and 1H NMR spectra. By using modified nanometer-sized alumina as micro-column packing material, a new method of flow injection (FI) on-line preconcentration coupled to ICP-OES was developed for simultaneous determination of trace metals (Ag, Pd, Au, Ga, In and Nb) in geological and environmental samples. The effects of pH, sample flow rate, sample volume, elution and interfering ions on the recovery of the analytes have been investigated. Under the optimized operating conditions, the adsorption capacity of the modified nanometer-sized alumina for Ag, Pd, Au, Ga, In and Nb were found to be 5.1, 7.6, 17.7, 15.6, 8.1 and 12.3 mg g−1, respectively. With 4 min preconcentration time and 24 s elution time, the enrichment factor was 10 and the sample frequency was 10 h−1. The detection limits of this method for Ag, Pd, Au, Ga, In and Nb were 0.12, 0.44, 0.27, 0.19, 0.54 and 0.18 μg l−1, respectively, while the R.S.D.s were 1.6, 2.3, 4.5, 1.6, 1.9 and 1.7% (n = 7, c = 50 ng ml−1), respectively. The proposed method has been applied to the determination of these trace metals in geological-certified reference materials and natural water samples with satisfactory results. 相似文献
986.
987.
Ji-Yen Cheng Chien-Chih Chiang Yah-Ru Cheng Hsuan-Shen Chen Leh-Jame Lin Ta-Chau Chang 《中国化学会会志》1997,44(2):97-100
The spectral features of satellite holes are used to investigate 9-aminoacridine-DNA interactions. The hole depths of the outer ring vibronic modes are reduced more than that of the inner ring vibronic modes, implying that inner ring motion is less perturbed than outer ring motion. As a result, the mode coupling between the inner ring and outer ring is reduced upon binding to DNA. However, similar hole frequency and width of the satellite hole corresponding to the NH2 mode upon binding to DNA imply that the amino group of 9-aminoacridine sits outside the DNA. 相似文献
988.
Streptomyces SP.N 14, isolated from soil samples, produced extracellular L-glutamate oxidase (GOD) in liquid culture. After
a two-step ammonium sulfate purification and dextran G-150 chromatography, the specific activity was reached at 28.2 U/mg.
The partial purified enzyme and horseradish peroxidase (HRP) were covalently coupled to alkylamine controlled pore glass (CPG)
by means of glutaraldehyde. About 200–300 U/g of immobilized GOD and 300–400 U/g of immobilized HRP were obtained. The immobilized
enzymes were packed into a teflon tube and used in flow injection analysis (FIA) for glutamate in broth. A good linear range
was observed for this immobilized enzyme system at 0.1–2.0 mM, and the precision was 2.8% (n = 25). More than 80 samples were measured within an hour. One enzyme column with about 4 U of immobilized GOD and 5 U of
immobilized HRP, applied for 50 assays/d, has been used for more than 50 d. The concentration of L-glutamate remaining lower
than 2.0 mM, the determination of glutamate in this system was not affected by pH and temperature within the range of 6.0–7.0
and 25–35‡C, respectively. The system was applied to determine L-glutamate in broth samples during L-glutamate fermentation,
and good correlation was achieved between results obtained with the system and with the Warburg’s method. 相似文献
989.
Immunoassay (IA) is a sensitive and selective approach for low level quantitation of drugs. Magnetic separation immunoassays use magnetic beads to facilitate the separation of bound labeled antigens from free antigens in solution. Digoxin was chosen for this study because low level analysis (ngmL–1) in biological samples isrequired, antibodies to digoxin were commercially available and derivatization procedures for fluorescence labeling were well established. A competitive immunoassay format was used in this study. Streptavidin coated magnetic beads were attached to biotinylated anti-digoxin antibodies for the separation. The inhibition curve for off-line magnetic separation immunoassay of digoxin in spiked plasma was characterized and the dynamic range of the curve was 0.25–2.5ngmL–1. A power fit weighted by the inverse of concentration was found to provide the best fit to the data (r=0.9934). The percent RSDs for the two controls, 0.8 and 2.2ngmL–1, were 9.95% and 20.62% (n=6) and the percent errors were 11.75% and 22.63% (n=6), respectively. The limit of detection (LOD) in plasma is 0.14ngmL–1. The dynamic range of the inhibition curve for on-line magnetic separation immunoassay of digoxin was 0.5–15ngmL–1 of digoxin. A quadratic fit was found to provide the best fit to the data (r=0.9937). The percent RSDs for the two controls, 4.0 and 12ngmL–1, were 14.1% and 10.7% (n=6) and the percent errors were 5.8% and 3.3% (n=6) from the spiked value, respectively. The LOD was estimated to be 0.44ngmL–1 (determined as two times the standard deviation of the blank, n=6). The on-line method has the advantages of being relatively easy to automate in the continuous flow mode and is adaptable for use in conjunction with HPLC separations. 相似文献
990.
This paper reports the development of a new approach for total phenol distillation using a focussed microwave oven, aiming its determination in petroleum refinery effluents and sour waters. In the procedure, 25 ml of sample is distilled during 15 min at 210 W power. At these conditions, recoveries as high as 95% are obtained, making possible the determination of total phenol in the samples without any interference and in a time significantly lower than that required by the reference method. In the course of the research, the influence of the distilled volume was investigated and a Doehlert matrix was employed for the multivariate optimization of the irradiation power and time. Quantification of phenol was spectrophotometrically performed in a FIA system, exploring classical reaction of phenol with 4-amineantipyrine and ferricyanide. Aqueous standards solutions of phenol could be directly injected in the FIA system for calibration purposes, making the procedure very simple and low time-consuming. A detection limit of 10 μg l−1 was achieved as well as a quantification limit of 33 μg l−1, becoming the procedure very suitable to be applied in the control of total phenols in effluents from petroleum industry. 相似文献