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11.
The partial molar volumes at infinite dilution of cryptand-222 (C-222) in water, methanol, acetonitrile, ethanol, dimethylsulfoxide, propanol, 2-propanol, chloroform, benzene, 1-butanol, cyclohexane, butyl-methylketone, hexane, tetrahydronaphthalene, heptane, octane, cyclohexylbenzene and decane were measured at concentrations ranging from 0.01 to 0.1 mol-L–1 at 25°C. The partial molar volumes at infinite dilution showed remarkable dependency on the molar volume of the solvent. The partial molar volumes at infinite dilution for C-222 increase as the solvent molar volume increases. 相似文献
12.
Lizhuang Zou Buxing Han Haike Yan K.L. Kasperski Yuming Xu L.G. Hepler 《Journal of colloid and interface science》1997,190(2):472
The enthalpies of adsorption and the isotherms for adsorption of naphthenic acid onto Na-montmorillonite, Na-kaolinite, and Na-illite were studied by means of calorimetry and the static method at 298.15 K. The results show that the enthalpies of adsorption and saturated adsorption amounts of naphthenic acid on different clays change in the order Na-montmorillonite > Na-illite > Na-kaolinite. The interaction between naphthenic acid and clays is discussed. 相似文献
13.
Ultra-trace analysis of U,Th, Ca and selected heavy metals in high purity refractory metals with isotope dilution mass spectrometry 总被引:1,自引:0,他引:1
A method for the determination of trace impurities (U, Th, Ca, Fe, Cr, Ni, Cu, and Cd) in the refractory metals molybdenum and tungsten with isotope dilution mass Spectrometry (IDMS) has been developed. This method enables determinations of uranium and thorium down to the lowest pg/g level with high precision and accuracy. Selective chromatographic, extractive and electrolytic methods for the trace-matrix separation were combined with positive thermal ionization mass spectrometry. Different samples of high purity (4N) and of ultra high purity (UHP) materials for advanced technologies were analysed. The detection limits reached are (in ng/g): U 0.006, Th 0.008, Ca 10, Fe 19, Cr 0.5, Ni 0.6, Cu 2.7, and Cd 0.12. A comparison of results with other sensitive analytical methods (ICP-MS, GDMS, SIMS) makes obvious the urgent necessity of a reliable calibration method like IDMS because the analytical results obtained by the other methods often spread over a wide range. 相似文献
14.
M. Fujisawa T. Matsushita Y. Matsui K. Akasaka T. Kimura 《Journal of Thermal Analysis and Calorimetry》2004,77(1):225-231
The heat capacities of binary aqueous solutions of 1,2-ethanediol, 1,2-propanediol and 1,2-butanediol were measured at temperatures
ranging from 283.15 to 338.15 K by differential scanning calorimetry. The partial molar heat capacities at the infinite dilution
were then calculated for the respective alkanediols. For 1,2-ethanediol or 1,2-propanediol, the partial molar heat capacities
at the infinite dilution of increased with increasing temperature. In contrast, the partial molar heat capacities of 1,2-butanediol
at the infinite dilution decreased with increasing temperature.
Heat capacity changes by dissolution of the alkanediols were also determined. Heat capacity changes caused by the dissolution
of 1,2-ethanediol or 1,2-propanediol were increase with increasing temperature. On the other hand, heat capacity changes caused
by the dissolution of 1,2-butanediol are decrease with increasing temperature. Thus our results indicated that the structural
changes of water caused by the dissolution of 1,2-butanediol differed from that of the two other alkanediols.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
15.
Monperrus M Tessier E Veschambre S Amouroux D Donard O 《Analytical and bioanalytical chemistry》2005,381(4):854-862
A robust method has been developed for simultaneous determination of mercury and butyltin compounds in aqueous samples. This method is capable of providing accurate results for analyte concentrations in the picogram per liter to nanogram per liter range. The simultaneous determination of the mercury and tin compounds is achieved by species-specific isotope dilution, derivatization, and gas chromatography–inductively coupled plasma mass spectrometer (GC–ICP–MS). In derivatization by ethylation and propylation, reaction conditions such as pH and the effect of chloride were carefully studied. Ethylation was found to be more sensitive to matrix effects, especially for mercury compounds. Propylation was thus the preferred derivatization method for simultaneous determination of organomercury and organotin compounds in environmental samples. The analytical method is highly accurate and precise, with RSD values of 1 and 3% for analyte concentrations in the picogram per liter to nanogram per liter range. By use of cleaning procedures and SIDMS blank measurements, detection limits in the range 10–60 pg L–1 were achieved; these are suitable for determination of background levels of these contaminants in environmental samples. This was demonstrated by using the method for analysis of real snow and seawater samples. This work illustrates the great advantage of species-specific isotope dilution for the validation of an analytical speciation method—the possibility of overcoming species transformations and non-quantitative recovery. Analysis time is saved by use of the simultaneous method, because of the use of a single sample-preparation procedure and one analysis. 相似文献
16.
The predictive accuracy for estimating infinite dilution activity coefficients by a modification of the UNIFAC method wherein the group interaction parameters were based on only data (referred to as -based UNIFAC) has been studied. Estimates and measured values were compared for six prototypical solutes in a series of homologous n-alkanes, l-alcohols and alkanenitrile solvents. Despite the fact that the interaction parameters were derived using only data, this approach still gave serious errors due to several inherent problems in the original UNIFAC model. Its performance is sometimes even poorer than that of the original UNIFAC method. For example for nitromethane in alcohols and p-dioxane in nitriles values predicted by the -based UNIFAC are essentially zero. The large errors for these systems are most likely due to inaccurate interaction parameters in the -based UNIFAC method. 相似文献
17.
The enthalpies of dilution of l-cystine in solutions of two strong alkalis and one strong acid have been determined by isothermal flow-mix calorimetry at the temperatures 298.15 K, 303.15 K, 308.15 K, 313.15 K and 318.15 K. Equations of apparent enthalpies of dilution have been obtained from the experimental data in terms of the improved McMillan-Mayer theory. Enthalpic interaction coefficients, h2, h3, and h4, are obtained and the values of pair-wise enthalpic interaction coefficient, h2, discussed in the light of solute-solute and solute-solvent interactions. 相似文献
18.
Enthalpies of dilution of aqueous systems containing formamide, dimethyl-formamide, the mixture of these amides, and each amide separately with mannitol, inositol, and cyclohexanol have been determined at 25°C. The data have been treated in terms of the Savage-Wood additivity principle and in combination with literature data. New values for the methylene-amide, carbinol-amide, and amide-amide group interaction enthalpies are presented. These may be used with data on a wider variety of solute systems to obtain interaction enthalpies for new groups. 相似文献
19.
An isotope dilution method for the determination of chloride ion in aqueous samples is described. The method makes use of the isotopic shift in the rotational lines of the 1–0 band of HCl emitted in the near infrared region of the spectrum by vibrationally excited HCl molecules present in a hydrogen/entrained air flame. Chloride ion in the sample is converted to chlorine gas by electrolysis and swept into a hydrogen/entrained air flame where it is converted into HCl. Because isotope dilution is an absolute method of analysis, matrix effects are minimized, and the chlorine generation step need not be quantitative. With the system described in this paper, samples must contain at least 9 mg of chloride ion per ml, and a 2-ml sample is required. Over the range from 10 to 30 mg Cl− ml−1, the average error was −0.96%, and the average relative standard deviation was 3.3% for seven samples using seven of the more intense lines in the P branch. Compared with standard silver nitrate titrations, the isotope dilution procedure was not affected by such common interferences as bromide ion and iodide ion. The technique was applied to several seawater samples from different regions. 相似文献
20.
氯化钙/水-醇溶液稀释热 总被引:3,自引:0,他引:3
电解质溶液稀释热是溶液的重要热性质之一.由它可计算不同浓度下电解质的溶解热、表现相对摩尔焓、溶液中反应热和化合物生成热等.在电解质溶液理论研究中,稀释热也是重要的基础数据.由稀释热可推算溶液中组分的活度系数、渗透系数、相对偏摩尔焓及表观摩尔热容等[1-3].在化工生产中,稀释热是化工过程能量计算不可缺少的数据.电解质水溶液稀释热已有不少研究[2,4].但电解质混合溶剂体系稀释热报导甚少.随着加盐精馏技术、海水淡化技术等研究的进展,急需这方面数据.本文作者已报告了CaCl2/C2H5OH-H2O体系[5]和CaCl2/n-C… 相似文献