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961.
Liandi Ma Liuxing Feng A. Hioki K. H. Cho J. Vogl A. Berger G. Turk S. Macleod G. Labarraque W. F. Tong D. Schiel C. Yafa L. Valiente L. A. Konopelko C. Quetel P. Vermaercke J. V. L. Manzano M. Linsky E. Cortés S. Tangpitayakul L. Plangsangmas L. Bergamaschi R. Hearn 《Accreditation and quality assurance》2010,15(1):39-44
The CCQM-P106 pilot study was organized by the inorganic working group of the Comité Consultatif pour la Quantité de Matière (CCQM) as a feasibility comparison to study the applicability of different analysis methods to the polypropylene sample and test the abilities of the participants for measuring the Cd, Cr, Hg and Pb in polypropylene. National Institute of Metrology P.R. China (NIM) acted as the coordinating laboratory of this pilot study. There were 21 laboratories that submitted the final results. The median values of the mass fraction of Cd, Cr, Hg and Pb were 36.12 mg kg?1 (the median absolute deviation about the median (MADe) = 0.46 mg kg?1), 252.5 mg kg?1 (MADe = 3.4 mg kg?1), 387.0 mg kg?1 (MADe = 10.1 mg kg?1) and 466.2 mg kg?1 (MADe = 8.9 mg kg?1), respectively. Isotope dilution mass spectrometry (IDMS), inductively coupled plasma-mass spectrometry (ICP-MS), inductively coupled plasma-optical emission spectrometry (ICP-OES), atomic absorption spectrometry (AAS), instrumental neutron activation analysis (INAA) and X-ray fluorescence (XRF) measurement methods were used, and microwave digestion was used by the most of the participants. In general, very good agreement of the results was observed. Moreover, compared to the results of other methods, the results of IDMS still showed less spread amongst laboratories and had a smaller uncertainty. In addition, the results of some analytes used by XRF and INAA also got satisfactory agreement with the median value. 相似文献
962.
Namgee Jung Yoon-Hwan Cho Kwang-Hyun Choi Ju Wan Lim Yong-Hun Cho Minjeh Ahn Yun Sik Kang Yung-Eun Sung 《Electrochemistry communications》2010,12(6):754-757
The cathode electrode structure of the direct methanol fuel cell (DMFC) was improved by a novel catalyst ink preparation method. Regulation of the solvent polarity in the cathode catalyst ink caused increases in the electrochemical active surface (EAS) for the oxygen reduction reaction (ORR) as well as decreases in the methanol crossover effect. In a two-step preparation, agglomerates consisting of catalyst and Nafion ionomers were decreased in size, and polar groups in the ionomers formed organized networks in the cathode catalyst layer. Despite Pt catalysts in the cathode being only 0.5 mg cm? 2, the maximum power density of the improved membrane electrode assembly (MEA) was 120 mW cm? 2, at 3 M methanol, which was much larger than that of traditional MEA (67 mW cm? 2). 相似文献
963.
Low and high molecular weight fucoidans (F(5-30K) and F(>30K)) were chemically modified through the addition of sulfate groups, and the effect of oversulfation on the in vitro anticancer activity was investigated. After the addition of sulfate groups, a considerable increase of 35.5 to 56.8% was observed in the sulfate content of the F(5-30K) fraction, while the sulfate content of the F(>30K) fraction increased to a lesser extent (from 31.7 to 41.2%). Significant differences in anticancer activity were observed between the oversulfated F(5-30K) and F(>30K) fractions, with activities of 37.3-68.0% and 20.6-35.8%, respectively. This variation in the anticancer activity of oversulfated fucoidan derivatives was likely due to differences in their sulfate content. The results suggest that the molecular conformation of these molecules is closely related to the extent of sulfation in the fucan backbones and that the sulfates are preferably substituted when the fucoidan polymers are in a loose molecular conformation. 相似文献
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967.
Chantiwas R Hupert ML Pullagurla SR Balamurugan S Tamarit-López J Park S Datta P Goettert J Cho YK Soper SA 《Lab on a chip》2010,10(23):3255-3264
Mixed-scale nano- and microfluidic networks were fabricated in thermoplastics using simple and robust methods that did not require the use of sophisticated equipment to produce the nanostructures. High-precision micromilling (HPMM) and photolithography were used to generate mixed-scale molding tools that were subsequently used for producing fluidic networks into thermoplastics such as poly(methyl methacrylate), PMMA, cyclic olefin copolymer, COC, and polycarbonate, PC. Nanoslit arrays were imprinted into the polymer using a nanoimprinting tool, which was composed of an optical mask with patterns that were 2-7 μm in width and a depth defined by the Cr layer (100 nm), which was deposited onto glass. The device also contained a microchannel network that was hot embossed into the polymer substrate using a metal molding tool prepared via HPMM. The mixed-scale device could also be used as a master to produce a polymer stamp, which was made from polydimethylsiloxane, PDMS, and used to generate the mixed-scale fluidic network in a single step. Thermal fusion bonding of the cover plate to the substrate at a temperature below their respective T(g) was accomplished by oxygen plasma treatment of both the substrate and cover plate, which significantly reduced thermally induced structural deformation during assembly: ~6% for PMMA and ~9% for COC nanoslits. The electrokinetic transport properties of double-stranded DNA (dsDNA) through the polymeric nanoslits (PMMA and COC) were carried out. In these polymer devices, the dsDNA demonstrated a field-dependent electrophoretic mobility with intermittent transport dynamics. DNA mobilities were found to be 8.2 ± 0.7 × 10(-4) cm(2) V(-1) s(-1) and 7.6 ± 0.6 × 10(-4) cm(2) V(-1) s(-1) for PMMA and COC, respectively, at a field strength of 25 V cm(-1). The extension factors for λ-DNA were 0.46 in PMMA and 0.53 in COC for the nanoslits (2-6% standard deviation). 相似文献
968.
Asymmetrical-flow field flow fractionation (AFFF) separates constituents based on hydrodynamic size and is emerging as a powerful
tool for obtaining high-resolution information on the size, molecular weight, composition, and stability of nanoscale particles
in liquid media. We employ a customized AFFF system combining on-line detectors for multi-angle light scattering, dynamic
light scattering, and UV–Vis absorption. Our objective is to develop optimized measurement protocols for the characterization
of gold nanoparticles (GNPs), which are widely utilized in biomedical research and other nanotechnology applications. Experimental
conditions have been optimized by controlling key parameters, including injection volume and solids concentration, mobile
phase composition, membrane type and pore size, and ratio of channel-to-cross-flow rates. Individual citrate-stabilized GNP
components (nominally 10, 20, 30, 40, and 60 nm) and GNPs functionalized with polyethylene glycol were separated from multicomponent
GNP mixtures by AFFF and subsequently characterized. We discuss the effects due to variations in measurement parameters and
GNP surface modification on observed retention, recovery, and peak resolution. 相似文献
969.
We propose three-dimensional (3D) optical microscopy using axially distributed image sensing. In the proposed method, the micro-objects are optically magnified and their axially distributed images are recorded by moving the image sensor along a common optical axis. The 3D volumetric images are generated from the recorded axial image set using a computational reconstruction algorithm based on ray backprojection. Preliminary experimental results are presented. To the best of our knowledge, this is the first report on 3D optical microscopy using axially distributed sensing. 相似文献
970.
Here we describe an anion excluding ion‐permeable membrane, which we evaluate on an O2‐electroreducing cathode poised at a strongly oxidizing potential, near the reversible potential of the O2/H2O half cell. The bioelectrocatalyst of the O2 cathode consists of the cross‐linked electrostatic adduct of a polycationic redox hydrogel and bilirubin oxidase (BOD), a polyanion at neutral at pH 7.3. If an uncured Nafion dispersion is applied on this bioelectrocatalyst, the polyanionic Nafion displaces the BOD in the electrostatic adduct, de‐wiring the BOD. We show here that insertion of a polycationic poly(acrylamide‐co‐vinylimidazole) (PAA‐PVI) between the bioelectrocatalyst and the Nafion prevents the dewiring of BOD. The resulting bi‐layer membrane effectively excludes the urate, thiocyanate and NADH anions. 相似文献