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1.
Correlations predicting frictional pressure drop and liquid holdup during horizontal gas-liquid pipe flow with a small liquid holdup 总被引:1,自引:0,他引:1
Experimental data and correlations available in the literature for the liquid holdup εL and the pressure gradient ΔPTP/L for gas-liquid pipe flow, generally, do not cover the domain 0 < εL < 0.06. Reliable pressure-drop correlations for this holdup range are important for calculating flow rates of natural gas, containing traces of condensate. In the present paper attention is focused on reliable measurements of εL and ΔPTPIL values and on the development of a phenomenological model for the liquid-holdup range 0 < εL < 0.06. This model is called the “apparent rough surface” model and is referred to as the ARS model. The experimental results presented in this paper refer to air-water and air-water + ethyleneglycol systems with varying transport properties in horizontal straight smooth glass tubes under steady-state conditions. The holdup and pressure gradient values predicted with the ARS model agree satisfactorily with both our experimental results and data obtained from the literature referring to small liquid-holdup values 0 < εL < 0.06. Further, it has been shown that in the domain 38 < < 72 mPa m the interfacial tension of the gas-liquid system has no significant effect on the liquid holdup. The pressure gradient, however, increases slightly with decreasing surface tension values. 相似文献
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The absorption spectra of a number of saturated hydrocarbons in the vacuum ultra-violet region have been examined and compared with their photoelectron and electron-loss spectra. Important conclusions about the quantum defect associated with the excited electrons and the nature of the excited states have been drawn from the relative positions of these spectra. The Rydberg bands of ethane, which were initially thought to originate in the C-C bond, have been shown to be associated with an electron largely localized in the CH3 group. 相似文献
6.
Chargaff’s second parity rule (CSPR) asserts that the frequencies of short polynucleotide chains are the same as those of
the complementary reversed chains. Up to now, this hypothesis has only been observed empirically and there is currently no
explanation for its presence in DNA strands. Here we argue that CSPR is a probabilistic consequence of the reverse complementarity
between paired strands, because the Gibbs distribution associated with the chemical energy between the bonds satisfies CSPR.
We develop a statistical test to study the validity of CSPR under the Gibbsian assumption and we apply it to a large set of
bacterial genomes taken from the GenBank repository. 相似文献
7.
Axial spatial distribution focusing: improving MALDI‐TOF/RTOF mass spectrometric performance for high‐energy collision‐induced dissociation of biomolecules 下载免费PDF全文
8.
Denis A. Brosnan John P. Sanders Stephanie A. Hart 《Journal of Thermal Analysis and Calorimetry》2011,106(1):109-115
Thermal analysis techniques have been used in characterizing building materials from significant historic properties in the
Charleston, South Carolina area. Determining the chemical and physical effects of deterioration resulting from long periods
of exposure is a first step in formulating preservation strategies. In this regard, simultaneous thermal analysis coupled
with evolved gas analysis has been used to study reactions between air, seawater, and masonry materials. Further, the traditional
petrographic identification of mortar composition is greatly facilitated through use of thermal analysis. Simultaneous thermal
analysis allows for an exact determination of the calcium carbonate content in mortars as an alternative to the use of an
inferred value based on chemical analysis data. The partial dissolution of calcium carbonate in the presence of sea salt is
a major deterioration process. Further, natural cements manufactured in the United States are identified, in part, based on
their thermogravimetric (TG) traces and their evolved gases. The data indicates that natural cements form some carbonate phases
in addition to the major hydrate phases. Clay bricks are found to exhibit interaction with sea water, with uptake of bicarbonate
suggested. Additionally, there is evidence of re-hydroxylation in the 160 year old bricks. The bricks made in coastal zones
contain a considerable free silica fraction that is composed of a small percentage of cristobalite. The silica content of
the clay bricks is seen to result in very high thermal expansion coefficients in the area of 10 × 10−6 to 12 × 10−6 K−1. These studies provide guidance in restoration efforts where authenticity of cements is important. In the event that replacement
bricks are required, matching the thermal expansion coefficient of the original bricks is a requirement for preservation of
the masonry structure. 相似文献
9.
David S. Hart Chithkala Harinarayan Gunnar Malmquist Andreas Axén Mandakini Sharma Robert van Reis 《Journal of chromatography. A》2009,1216(20):4372-4376
Increased recombinant protein expression yields and a large installed base of manufacturing facilities designed for smaller bulk sizes has led to the need for high capacity chromatographic resins. This work explores the impact of three pore sizes (with dextran distribution coefficients of 0.4, 0.53, and 0.64), dextran surface extender concentration (11–20 mg/mL), and ligand density (77–138 μmol H+/mL resin) of cation exchange resins on the dynamic binding capacity of a therapeutic antibody. An intermediate optimal pore size was identified from three pore sizes examined. Increasing ligand density was shown to increase the critical ionic strength, while increasing dextran content increased dynamic binding capacity mainly at the optimal pore size and lower conductivities. Dynamic binding capacity as high as 200 mg/mL was obtained at the optimum pore size and dextran content. 相似文献
10.
William D. Banks Derrick N. Hart Pieter Moree C. Wesley Nevans 《Monatshefte für Mathematik》2009,1(1):303-322
In 1984, G. Robin proved that the Riemann hypothesis is true if and only if the Robin inequality σ(n) < e
γ
n log log n holds for every integer n > 5040, where σ(n) is the sum of divisors function, and γ is the Euler–Mascheroni constant. We exhibit a broad class of subsets S{\mathcal {S}} of the natural numbers such that the Robin inequality holds for all but finitely many n ? S{n \in \mathcal {S}} . As a special case, we determine the finitely many numbers of the form n = a
2 + b
2 that do not satisfy the Robin inequality. In fact, we prove our assertions with the Nicolas inequality n/φ(n) < e
γ
log log n; since σ(n)/n < n/φ(n) for n > 1 our results for the Robin inequality follow at once. 相似文献