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101.
Sonia Natale 《Algebras and Representation Theory》2002,5(5):445-455
We conclude the classification of Hopf algebras of dimension 12 over an algebraically closed field of characteristic zero. 相似文献
102.
Przemysław Bartczak Sonia Żółtowska Małgorzata Norman Łukasz Klapiszewski Jakub Zdarta Andrzej Komosa Ignacy Kitowski Filip Ciesielczyk Teofil Jesionowski 《Adsorption》2016,22(4-6):517-529
For the first time in the published literature, a study is described concerning the use of the saw-sedge Cladium mariscus (C. mariscus) for adsorption of 2,4-dichlorophenoxyacetic acid (2,4-D) from aqueous systems. Among the experiments carried out, the elemental composition of C. mariscus was determined (C = 48.0 %, H = 7.1 %, N = 0.95 %, S = 0.4 %), FTIR spectroscopic analysis was performed to confirm the chemical structure of the adsorbent, and porous structure parameters were measured: BET surface area (A BET = 0.6 m2/g), total pore volume (V p = 0.001 cm3/g) and average pore size (S p = 6.6 nm). It was shown that the effectiveness of removal of 2,4-D from aqueous systems using C. mariscus depends on parameters of the process: contact time, system pH, mass of sorbent, and temperature. Maximum adsorption was attained for a solution at pH = 3. Further increase in the alkalinity of the tested systems led to a reduction in the effectiveness of the process. The kinetic of adsorption of 2,4-D by C. mariscus was also determined, and thermodynamic aspects were investigated. The experimental data obtained correspond to a pseudo-second-order kinetic model of type 1. Additionally the negative values obtained for ΔHº indicate that the process is exothermic, and the negative values of ΔGº show it to be spontaneous. As the temperature of the system increases the spontaneity of adsorption is reduced, in accordance with the exothermic nature of the process. 相似文献
103.
104.
Sonia Ben Abdelkhalek Nabil Kallel Sami Kallel Octavio Peña Mohamed Oumezzine 《Journal of magnetism and magnetic materials》2012
Critical behavior in the La0.6Sr0.4Mn0.8Fe0.1Cr0.1O3 ceramics was studied using magnetization methods. Results show that the paramagnetic–ferromagnetic transition is of second order. Based on the critical behavior analysis using the Banerjee criterion and the Kouvel–Fisher method, we find the critical exponents: β=0.395±0.010, γ=1.402±0.010, and δ=5.208±0.007, for which the magnetic interaction is satisfied within the three-dimensional Heisenberg model. Results indicate the presence of short-range interactions. The magnetic entropy change (−ΔSM) reached maximum values of 1.75, 1.45, 1.15, 0.8 and 0.43 J Kg−1 K−1 under a magnetic field variation of 5, 4, 3, 2 and 1 T, respectively. Nevertheless, these (−ΔSM) values are much low for any potential application at this moment. The nature of this phenomenon is discussed in relation to the characteristics of the magnetic phase transition and critical exponents. 相似文献
105.
Sonia Natale 《Algebras and Representation Theory》2010,13(6):673-691
We determine the structure of Hopf algebras that admit an extension of a group algebra by the cyclic group of order 2. We
study the corepresentation theory of such Hopf algebras, which provide a generalization, at the Hopf algebra level, of the
so called Tambara-Yamagami fusion categories. As a byproduct, we show that every semisimple Hopf algebra of dimension < 36
is necessarily group-theoretical; thus 36 is the smallest possible dimension where a non group-theoretical example occurs. 相似文献
106.
Losada C Albertí JJ Saurina J Sentellas S 《Analytical and bioanalytical chemistry》2012,404(2):539-551
Recently, liquid chromatography coupled to inductively coupled plasma mass spectrometry (LC-ICP/MS) has been introduced to deal with some applications in the field of pharmaceutical, biomedical, and clinical analysis. In the case of drug research, the number of drugs and their metabolites containing detectable elements is quite limited. In this paper, LC-ICP/MS has been demonstrated to be suitable for the determination of S-containing drugs and their metabolites. In order to minimize the interference of polyatomic oxygen (m/z 32), the indirect detection of S, by means of the SO(+) ion (m/z 48), was optimized. For quantification purposes, it has been encountered that the percentage of organic solvent in the mobile phase strongly affects the sensitivity. Here, corrective strategies based on calibration curves established at different solvent concentrations (solvent-zone quantification) and post-column gradient compensation have been proposed to circumvent sensitivity variations. Results obtained have shown that suitable calibration models have been built for any compound regardless of the solvent percentage at which it is eluted from the chromatographic column. To prove the applicability of this methodology, the metabolism of ethacrynic acid and tiotropium bromide has been studied in vitro and in vivo. In the first case, ethacrynic acid does not contain S in its structure, however, the major route of metabolism for this compound consists of the formation of glutathione adduct and its further degradation. In the second case, tiotropium bromide contains two S atoms in its structure. 相似文献
107.
Del Sordo Filho Giovanni Torrecilha Jefferson Koyaishi Scapin Marcos Antônio Oliveira Sonia Maria Barros da Silva Paulo Sergio Cardoso 《Journal of Radioanalytical and Nuclear Chemistry》2021,329(1):61-70
Journal of Radioanalytical and Nuclear Chemistry - This study has evaluated chemical, radiological composition and determined the cation exchange capacity (CEC) for three commercially available... 相似文献
108.
Coriani S Thorvaldsen AJ Kristensen K Jørgensen P 《Physical chemistry chemical physics : PCCP》2011,13(10):4224-4229
The atomic axial tensor (AAT) of vibrational circular dichroism is expressed as the frequency derivative at zero frequency of a linear response function for operators referencing a nuclear displacement and a magnetic field. This is used in the density matrix-based quasienergy derivative Lagrangian approach of Thorvaldsen et al. [J. Chem. Phys., 2008, 129, 214108] to express the AAT in a form where the need to solve response equations for the nuclear displacements is removed, significantly reducing the computation cost compared to existing formulations. The density matrix-based quasienergy derivative Lagrangian approach also allows us straightforwardly to use London atomic orbitals to remove the gauge-origin dependence and to account for the atomic orbitals' dependence on the nuclear coordinates. The formalism is entirely based on atomic-orbital density and integral matrices and therefore amenable to linear scaling for sufficiently sparse matrices and given a linearly scaling response solver. 相似文献
109.
María Sáenz José Alvarado Francisco Pena-Pereira Sonia Senra-Ferreiro Isela Lavilla Carlos Bendicho 《Analytica chimica acta》2011,(1):50
A new miniaturized methodology based on the combination of headspace single drop microextraction and microvolume fluorospectrometry is proposed in this work for the determination of free and hydrolyzed formaldehyde in textile samples. The proposed method is based on the extraction and in-drop derivatization of free and hydrolyzed formaldehyde using the Hantzsch reaction. The effect of experimental variables affecting the performance of the proposed method, such as fluorescence parameters, nature of the extractant phase composition (including acetylacetone concentration, pH, ammonium acetate concentration and presence of an organic solvent), sample temperature, NaCl concentration and microextraction time was carefully investigated. Under optimized conditions, instrumental detection and quantification limits were 26 and 87 μg L−1, respectively, whereas procedural detection and quantification limits were 1.0 and 3.5 mg kg−1, respectively. Repeatability, expressed as relative standard deviation, was 4.6% (n = 9). The method was successfully applied to the determination of free and hydrolyzed formaldehyde in several textile samples, the found results being in good agreement with those obtained with the EN ISO 14184-1:1998 method. 相似文献
110.
Three new tetracyclic polyisoprenylated xanthones, named oxy-guttiferones M, K2, and I, along with oxy-guttiferone K and guttiferone M, have been isolated from the fruits of Garcinia cambogia. Their structures were elucidated by MS and NMR spectroscopic experiments. The absolute configurations of oxy-guttiferone K, taken as a model of tetracyclic xanthones, and guttiferone M, as a model of polyisoprenylated benzophenones, have been determined by comparison of their experimentally measured circular dichroism (CD) curves with the TDDFT-predicted curves. 相似文献