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This paper describes a novel approach to detect Cd(II) using the combination of the differential pulse anodic stripping voltammetry and magnetic nanoparticle based dispersive solid phase microextraction as an efficient, green and accurate method. Currents of Cd(II) increased linearly in the range from 75 to 2000 ng L−1 Cd(II) with a detection limit of 21.6 ng L−1. The RSD values of 2.6 and 6.0 % for 1.00 and 0.10 μg L−1 respectively showed that proposed method has an acceptable repeatability. Recovery values between 92.3 and 98.6 % showed that this approach can be successfully used for determination of Cd(II) in water samples. 相似文献
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This study was undertaken to establish one of the most reliable sampling methods and to precisely evaluate the bias involved in the collection of airborne pollutant samples. For the purpose of our study, we investigated the performance of three different types of sampling techniques by measuring major aromatic volatile organic compounds (VOC) in outdoor air; the target analytes specifically include benzene, toluene, ethylbenzene, and xylene (commonly called BTEX). As the first step of our approach, we designed and developed a multi-channel sampling system consisting of a six-port mass flow controller (SJU-MFC) system. Because this system allowed the collection of up to six replicate samples, our measurement results were analyzed and screened statistically for the derivation of high-quality BTEX data. The feasibility of this sampling system was further tested through a comparison with concurrent measurement data sets obtained by two additional, but independent, sampling techniques: (1) automatic continuous sampler (ACS) and (2) on-line GC (O-GC) system. Based on the data sets collected concurrently by three different sampling methods, we attempted to evaluate the compatibility of sampling techniques. Although the results obtained by SJU-MFC system were not statistically different from those of the O-GC system, they were moderately distinguishable from those of ACS. Such patterns were seen consistently, when examined by correlation analysis. The overall results of our study thus generally point out that the compatibility of data sets, when the proper caution is taken, improve significantly among different sampling methodologies. 相似文献
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Work function (WF) of undoped and Gd-doped PbZrO3 (PZG) was determined during isothermal oxidation and reduction experiments at 400 and 500 °C in the P(O2) range between 10 and 2.1×104 Pa. The obtained results are discussed in terms of two competitive effects, such as (i) an acceptor-type effect due to oxygen
chemisorption and its subsequent incorporation into the oxide lattice and (ii) donor-type effect due to p(O2)-induced structural transitions, such as decomposition of PbZrO3 resulting in the formation of a surface layer composed of PbO and ZrO2. Both effects have different rates of appearence and the effect on electrical potential. It was found that oxidation results
in irreproducible changes of surface properties involving the formation of a low-dimensional surface layer. 相似文献
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This work reports the gas/solid equilibration kinetics for the O2/CaTiO3 system. The electrical conductivity measurement was applied for monitoring the kinetics in the ranges of temperature 973-1323 K and oxygen partial pressure 10 Pa-72 kPa. It was found that the gas/solid equilibration kinetics for the polycrystalline CaTiO3 specimen in the above experimental conditions is determined by bulk diffusion rather than by grain boundary conditions. The obtained data of the electrical conductivity vs. time were used for the determination of the chemical diffusion coefficient as a function of temperature at low and high p(O2), respectively:
(1) 相似文献
19.
The primary purpose of the present work is the determination of the thermopower component related to electronic charge carriers for undoped calcium titanate. The second purpose of this work is establishment of the relationship between this thermopower component and the electronic component of electrical conductivity. An essential part of the present study includes the determination of the thermopower components corresponding to different charge carriers (electrons, electron holes and ions). The determination procedures are based on the following three models: Symmetrical model. This model assumes consistency between thermopower and electrical conuctivity in terms of the n-p transition (this model assumes that minimum of electrical conductivity corresponds to the electronic component of the thermopower equal zero). It was shown that this model does not apply for CaTiO3. The Heikes model. This model is based on Heikes formula and also hopping mechanism of the transport of electrons. It was shown that thermopower of CaTiO3 cannot be described by this model and, consequently, thermopower vs. electrical conductivity cannot be considered within the Jonker formalism. General model. This model is based on a general thermopower equation for mixed conductors without any simplifying assumptions. Application of this model indicates that the electronic component of thermopower is not consistent with the minimum of electrical conductivity. 相似文献
20.
Tibor Novák Péter Bakó György Keglevich András Dobó Károly Vékey László Tóke 《Journal of inclusion phenomena and macrocyclic chemistry》2001,40(3):207-212
Five chiral -D-glucose-based monoaza-15-crown-5 ethers with phosphinoxidoalkyl side chains of one to five carbon atoms (5a–e)have been synthesised. The cation binding ability of the new lariat ethers was evaluated bythe picrate extraction method. The substituents at the nitrogen atom were not a major influenceon the cation extraction ability of the azacrown ether; the compounds showed, however, a significant asymmetric induction as phase transfer catalysts in the Michael addition of2-nitropropane to chalcone (95% ee). 相似文献