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51.
研究了原子化器温度、载气流速、KBH4 浓度等条件对流动注射 氢化物发生 原子吸收光谱法 (FI-HG -AAS)测定硒时的影响。建立了FI-HG -AAS测定大米中硒的分析方法。在优化的工作条件下 ,测定硒的最低检测浓度为 0 3 3 μg·L- 1,线性范围为 0~ 5 0 μg·L- 1,相对标准偏差小于 4% ,加标回收率为 94%~ 1 0 2 %。本法克服了传统的间断氢化物发生 原子吸收光谱法分析速度慢、样品耗量大、操作繁琐且因手工进样在进样速度和进样体积上容易带来误差等缺点。方法操作简便、快速 ,灵敏度及自动化程度高 ,已广泛应用于大米及富硒大米中微量硒的测定 相似文献
52.
Adrenaline was found to inhibit strongly the electrochemiluminescence (ECL) from the Ru(bpy)32+/tripropylamine system when a working Pt electrode was maintained at 1.05 V (versus Ag/AgCl) in pH 8.0 phosphate buffer. On this basis, a flow injection (FI) procedure with inhibited electrochemiluminescence detection has been developed for determination of adrenaline. The method exhibited a good reproducibility, sensitivity, and stability with a detection limit (signal-to-noise ratio = 3) of 7.0×10−9 mol l−1 and dynamic concentration range of 2×10−8 to 1×10−4 mol l−1. The relative standard deviation was 2.2% for 1.0×10−6 mol l−1 adrenaline (n=11). The method was successfully applied to the determination of adrenaline in pharmaceutical samples. Moreover, ECL emission spectra, UV-Vis absorption spectra and cyclic voltammograms of Ru(bpy)32+/tripropylamine/adrenaline were studied. The inhibition mechanism has been proposed as the interaction of electrogenerated Ru(bpy)32+* and the o-benzoquinone derivatives, adrenochrome and adrenalinequinone, at the electrode surface. 相似文献
53.
54.
The development of iodide-based methods for batch and on-line determinations of phosphite in aqueous samples 总被引:2,自引:0,他引:2
Recent developments in the field of microbiology and research on the origin of life have suggested a possible significant role for reduced, inorganic forms of phosphorus (P) such as phosphite [HPO32−, P(+III)] and hypophosphite [H2PO2−, P(+I)] in the biogeochemical cycling of P. New, robust methods are required for the detection of reduced P compounds in order to confirm the importance of these species in the overall cycling of P in the environment. To this end, we have developed new batch and flow injection (FI) methods for the determination of P(+III) in aqueous solutions. The batch method is based on the reaction of P(+III) with a mixed-iodide solution containing tri-iodide (I3−) and penta-iodide (I5−). The oxidation of P(+III) consumes free I3− and I5− in solution. The remaining I3− and I5− subunits are then allowed to react with the amylose content in starch to form a blue complex, which has a λmax of 580 nm. The measurement of this blue complex is directly correlated with the concentration of P(+III). The on-line FI method employs the same reaction between P(+III) and mixed-iodide producing phosphate [P(+V)] that is determined spectrophotometrically by the molybdenum blue method employing ascorbic acid at a λmax of 710 nm. The linear range for both the batch and FI determination of P(+III) was 1.0–50 μM with detection limits of 0.70 and 0.36 μM, respectively. Interference studies for the batch method show that arsenite [As(+III)] and sulfite [S(+IV)] can also be determined by this technique; however, these interferences can be circumvented by oxidizing As(+III) and S(+IV) using KMnO4 which is an ineffective oxidant for P(+III). Both methods were applied to P(+III) determinations in ultra-pure water and simulated creek water. Results and analytical figures of merit are reported and future work is considered. 相似文献
55.
Automated flow-based anion-exchange method for high-throughput isolation and real-time monitoring of RuBisCO in plant extracts 总被引:1,自引:0,他引:1
In this work, a miniaturized, completely enclosed multisyringe-flow system is proposed for high-throughput purification of RuBisCO from Triticum aestivum extracts. The automated method capitalizes on the uptake of the target protein at 4 °C onto Q-Sepharose Fast Flow strong anion-exchanger packed in a cylindrical microcolumn (105 × 4 mm) followed by a stepwise ionic-strength gradient elution (0-0.8 mol/L NaCl) to eliminate concomitant extract components and retrieve highly purified RuBisCO. The manifold is furnished downstream with a flow-through diode-array UV/vis spectrophotometer for real-time monitoring of the column effluent at the protein-specific wavelength of 280 nm to detect the elution of RuBisCO. Quantitation of RuBisCO and total soluble proteins in the eluate fractions were undertaken using polyacrylamide gel electrophoresis (PAGE) and the spectrophotometric Bradford assay, respectively. A comprehensive investigation of the effect of distinct concentration gradients on the isolation of RuBisCO and experimental conditions (namely, type of resin, column dimensions and mobile-phase flow rate) upon column capacity and analyte breakthrough was effected. The assembled set-up was aimed to critically ascertain the efficiency of preliminary batchwise pre-treatments of crude plant extracts (viz., polyethylenglycol (PEG) precipitation, ammonium sulphate precipitation and sucrose gradient centrifugation) in terms of RuBisCO purification and absolute recovery prior to automated anion-exchange column separation. Under the optimum physical and chemical conditions, the flow-through column system is able to admit crude plant extracts and gives rise to RuBisCO purification yields better than 75%, which might be increased up to 96 ± 9% with a prior PEG fractionation followed by sucrose gradient step. 相似文献
56.
Picomole‐level Formaldehyde Determination in Gaseous and Beer Samples Using Flow Injection Chemiluminescence Analysis 下载免费PDF全文
Based on the linear enhancement of formaldehyde (FA) within 7.0 ~ 1000 pmol l?1 on luminol—bovine serum albumin (BSA) chemiluminescence (CL) system, FA determination in air and beer samples using CL with flow injection (FI) was proposed. The detection limit was 2.5 pmol l?1 (3σ) and the relative standard deviations were less than 4.5% (n = 7). At a flow rate of 2.0 mL min?1, a whole analysis from sampling to washing only needed 32 s, offering a sample throughput of 112 h?1. This proposed method was successfully utilized to determine FA vapor pressure in liquid (121.8 ± 3.8 Pa), FA content in real air sample (8.93 ± 0.03 mg m?3), and FA levels in beer (199.5 ± 5.6 ~ 225.2 ± 3.5 mg l?1), giving determination recoveries from 90.7% to 109.3%. The mechanism of BSA—FA interaction was also investigated, showing FA binding to BSA was a spontaneous process mainly through hydrogen bonding and van der Waals force by FI‐CL, with binding constant K of 1.89 × 106 l mol?1 and the number of binding sites n of 0.86. Molecular docking analysis further revealed FA could enter into the pocket at subdomain IIA of BSA, with K of 1.71 × 105 l mol?1 and ΔG of ‐29.68 kJ mol?1. 相似文献
57.
采用溶胶凝胶技术对 Luminol- Co( ) - H2 O2 体系中的 Co( )和 Luminol试剂进行了固定化 ,并将其用于化学发光法测定 H2 O2 。试验结果表明 ,固定柱的洗脱液中 Co( )的浓度稳定 ,测定的线性范围为 2× 1 0 - 6~ 1× 1 0 - 4 mol·L- 1 ,相关系数大于 0 .997,检出限为 0 .6μmol·L- 1 。1 0次测定的 RSD为 1 .7% ,单次测定能在 1 min内完成。方法成功地用于雨水中 H2 O2 的测定。 相似文献
58.
Roman Mikhailov 《代数通讯》2013,41(7):2191-2207
Given a group Π, we study the group homology of centralizers Π g , g ? Π, and of their central quotients Π g /〈 g〉. This study is motivated by the structure of the Hochschild and the cyclic homology of group algebras, and is based on Quillen's approach to the cyclic homology of algebras via algebra extensions. A method of computing the de Rham complex of a group algebra by means of a Gruenberg resolution is also developed. 相似文献
59.
Non-attendance to meaning by students is a prevalent phenomenon in school mathematics. Our goal is to investigate features of instruction that might account for this phenomenon. Drawing on a case study of two high school algebra teachers, we cite episodes from the classroom to illustrate particular teaching actions that de-emphasize meaning. We categorize these actions as pertaining to (a) purpose of new concepts, (b) distinctions in mathematics, (c) mathematical terminology, and (d) mathematical symbols. The specificity of the actions that we identify allows us to suggest several conjectures as to the impact of the teaching practices observed on student learning: that students will develop the belief that mathematics involves executing standard procedures much more than meaning and reasoning, that students will come to see mathematical definitions and results as coincidental or arbitrary, and that students’ treatment of symbols will be largely non-referential. 相似文献
60.
The induction theory for a Hopf group coalgebra is outlined. Given a Hopf group coalgebra H, the notions of a quotient Hopf group coalgebra and group coisotropic quantum subgroup of H are introduced. The properties of (co)induced representations are studied and the geometric interpretation and simplicity
theory of such representations are given.
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