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141.
通过表面张力和等温滴定量热方法,研究了非离子表面活性剂Tween-20与牛血清白蛋白(BSA)的相互作用. 结果表明,BSA与Tween-20的相互作用较弱,当Tween-20浓度增大时,能将吸附于表面上的BSA分子取代. BSA/Tween-20混合体系的性质随温度的变化趋势与单一非离子型表面活性剂相似. BSA浓度在3.7×10-5~11.1×10-5 kg•L-1范围内,Tween-20的cmc不随BSA浓度的变化而变化. 当Tween-20的含量一定时,Tween-20与BSA相互作用过程的热效应也与BSA 的浓度无关. BSA/Tween-20混合体系的热力学参数表明, BSA的存在使Tween-20的cmc减小,体系的熵变增大. 相似文献
142.
2-(8-羟基喹啉-5-磺酸-7-偶氮)-1,8-二羟基-3,6-萘二磺酸与牛血清白蛋白的相互作用 总被引:5,自引:0,他引:5
用平衡透析法和分光光度法研究了 2 (8 羟基喹啉 5 磺酸 7 偶氮 ) 1,8 二羟基 3,6 萘二磺酸与牛血清白蛋白 (BSA)在酸性溶液中的结合反应 ,认为 8Q5SAC与BSA之间的结合力是以静电引力为主的非共键作用力 ,并探讨了其结合模型。在 2 98K下 ,测得这一反应的最大结合数为 35~ 40 ,结合常数为 6 .1× 10 5L mol。还研究了溶液基本条件如酸度和离子强度等对 8Q5SAC与牛血清白蛋白分子复合物形成的影响 ,在pH =3.34条件下 ,标准工作曲线的线性范围为 0 .2 0~ 46 .90mg L。 相似文献
143.
Utilization of ferric chelate complex of trans-1,2-cyclohexanediaminetetraacetic acid (CDTA) for the oxidative scrubbing of H2S and CH3SH in Kraft mill streams can be beneficial from the standpoints of iron protection against precipitation and oxygen-mediated regenerative oxidation of the ferrous chelate CDTA. The physical solubility of methyl mercaptan in CDTA–Fe(III) complex cannot be measured directly because of oxidation of the sulfur-bearing gaseous species with the ferric chelate. Therefore, this investigation was carried out to determine the gas–liquid partition coefficients and Henry's law constants of methyl mercaptan in aqueous iron-free CDTA solutions and non-reacting ferrous chelate solutions (CDTA–Fe(II) complex), using the static headspace method with an estimated accuracy of about 2%. Experiments with aqueous solutions of chelate concentrations varying between 38 and 300 mol m−3 were carried out at temperatures between 298 and 333 K and atmospheric pressure. It was shown that the methyl mercaptan solubility decreases with increasing temperature for all systems but was not much influenced, in the studied conditions, by the chelate concentration especially at larger temperatures. 相似文献
144.
Hitoshi?MatsukiEmail author Michio?Yamanaka Hiroshi?Kamaya Shoji?Kaneshina Issaku?Ueda 《Colloid and polymer science》2005,283(5):512-520
The dissociation equilibrium between uncharged local anesthetic lidocaine (LC) and charged local anesthetic LC (LCH+) in a surface-adsorbed film was investigated by measuring the surface tension and pH of aqueous solutions of a mixture of hydrochloric acid and LC. The surface tension values decreased slightly with increasing total molality mt at 0X20.5, where X2 is the mole fraction of LC in the mixture, while they decreased rapidly with increasing mt at 0.5<X21. It was shown from the pH measurements that almost all LC molecules were changed into LCH+ ions by protonation at 0X20.5 and both forms coexisted only at 0.5<X21. The quantities of the respective LC and LCH+ transferred from the aqueous solution to the adsorbed film, i.e., their surface densities, were calculated by applying the thermodynamic equations derived to the surface tension and pH data. A greater quantity of LC than LCH+ existed in the adsorbed film at the coexisting composition. The partitioning behavior of LC and LCH+ in the adsorbed film was characterized by three composition regions: (1) slight partitioning of low surface-active LCH+ in the region at 0X20.5, (2) preferential partitioning of LC at 0.5<X2<around 0.7, and (3) negative partitioning of LCH+ at around 0.7X21. The present results clearly indicate that uncharged local anesthetics transfer into hydrophobic environments such as cell membranes more than charged ones. 相似文献
145.
CNDO/force calculations have been employed to calculate the O-H stretching force constants for various structures of associated
water species such as water-dimethylether, water-acetonitrile, water-lithium fluoride, linear and cyclic water polymers. The
variation in the O-H stretching force constant in Am… O-H… Dn species where Am
and Dn represent, respectively,m number of electron-acceptor andn number of electron-donor molecules, is explained on the basis of the cooperativity effect. With increasing electron-acceptor
power of A and electron-donor power of D, the hydrogen-bonded O-H stretching force constant is significantly reduced. The
results obtained in these studies are in general agreement with experimental observations reported earlier. 相似文献
146.
恒电流库仑法测定基准试剂三氧化二砷的含量 总被引:2,自引:0,他引:2
用恒电流库仑法测定基准试剂三氧化二砷的含量,以恒电流通过含有碘化钾,基准试剂三氧化二砷试样的弱碱性水溶液,利用工作电极铂阳极上电生滴定剂I2与亚砷酸盐定量反应,以死停终点法确定滴定终点,测量出电解电流和电解时间,根据法拉第电解定律并利用EXCEL计算出基准试剂三氧化二砷的含量。方法的回收率为100%。 相似文献
147.
E. U. Franck 《Journal of solution chemistry》1973,2(2-3):339-356
A survey is given of recent experimental results obtained from high-temperature, high-pressure investigations with water, aqueous solutions, and ionic fluids. Data on the static dielectric constant of water to 550°C and 5 kbar are given and discussed with respect to their relation to water structure. Infrared and Raman spectra of HDO in pure water have been obtained to 400°C and 4 kbar, which give information on hydrogen bonding. Xe–H2O and CO2–H2O mixtures were investigated in the infrared. Ni(II) and Cu(II) complexes were investigated by absorption spectroscopy in aqueous solutions of high chloride content to 350°C and 2–6 kbar. The gas-liquid critical point of ammonium chloride was found at 880°C and 1635 bars. This fluid appears to be predominantly ionic even in the critical region. The possibility of converting pure polar fluids such as ammonia and water into concentrated ionic solutions by self-ionization at very high pressures is mentioned.This paper was presented at the symposium, The Physical Chemistry of Aqueous Systems, held at the University of Pittsburgh, Pittsburgh, Pennsylvania, June 12–14, 1972, in honor of the 70th birthday of Professor H. S. Frank. 相似文献
148.
Interfacial layers have been widely applied to study the formation and stability of emulsion-based systems. However, the application of isolated interfaces to address digestibility of emulsions is often limited because of the complexity of experimental methods and results. This review summarizes the latest developments in analytical methods and literature data on effects of digestion on interfacial layers. Particular emphasis is given to understand the changes on interfacial magnitudes during oral, gastric, and duodenal digestion, either applied separately or sequentially. Limitations of interfacial aspects and key factors that influence emulsion microstructure in bulk and lipid digestion are identified. Understanding the behavior of interfacial layers upon gastrointestinal digestion promotes an accurate tracking of the physiological fate of emulsions. 相似文献
149.
Yasuyuki Takeda Chihiro Takagi 《Journal of inclusion phenomena and macrocyclic chemistry》1994,17(1):93-97
The theory is derived to determine the dimer-formation constant,K
2, of a crown ethermetal salt 111 complex in organic solvents of low dielectric constant by solvent extraction. The theoretical predictions are verified experimentally by extraction of sodium picrate (NaA) with 15-crown-5 (15C5) into carbon tetrachloride. All the experiments were conducted at 25°C. The logK
2 value of the Na(15C5)A complex in carbon tetrachloride has been determined to be 4.05±0.11. Moreover, the partition constant of the complex is calculated. 相似文献
150.
M. Paluch 《Colloid and polymer science》1998,276(7):648-652
The results of experimental studies of the adsorption at the solution/air interface from an aqueous mixture: 2,4,6-trimethylphenol–2,4,6-trichlorophenol
are presented. The surface properties of the above-mentioned mixture were studied by surface potential and surface tension
measurements. These measurements were carried out as a function of the concentration of 2,4,6-trimethylphenol aqueous solution
at a constant concentration of 2,4,6-trichlorophenol.
Using the results obtained and based on the Gibbs equation, Helmholtz formula and Motomura’s method the relative surface excesses
of adsorbed substances, effective dipole moments, surface molar fractions of solutes and miscibility of adsorbed films were
determined.
Received: 7 November 1997 Accepted: 26 February 1998 相似文献