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71.
The maximum number of non-vanishing and independent second order photoelastic coefficients required by the seven pentagonal
and the two icosahedral point groups 5(C5),
(S10),
(C5h
),
m2(D5h
), 52(D5), 5m(C5v
),
2m(D5d
); 235(I), 2/m
(I
h
)—that describe the quasicrystals symmetry groups in two and three dimensions—is obtained. The schemes of non-vanishing and
independent coefficients have been calculated and listed. Finally the results of this group-theoretical study are briefly
discussed. 相似文献
72.
The transport coefficients for the nine point groups
—which represent the symmetry groups of the quasicrystals in two and three dimensions—have been evaluated and tabulated in
this work, employing group-theoretical methods. 相似文献
73.
The Balancing Domain Decomposition algorithm uses in each iteration solution of local problems on the subdomains coupled with a coarse problem that is used to propagate the error globally and to guarantee that the possibly singular local problems are consistent. The abstract theory introduced recently by the first-named author is used to develop condition number bounds for conforming linear elements in two and three dimensions. The bounds are independent of arbitrary coefficient jumps between subdomains and of the number of subdomains, and grow only as the squared logarithm of the mesh size . Computational experiments for two- and three-dimensional problems confirm the theory.
74.
Ramakrishna P. Bhat 《Tetrahedron letters》2005,46(28):4801-4803
β-Acetylamino ketones have been obtained in a one-pot coupling of an aldehyde with an enolisable ketone, acetyl chloride and acetonitrile in the presence of zeolite Hβ as catalyst at room temperature (26-28 °C). The procedure has the advantages of mild workup, circumvention of high temperature and inert atmosphere. The catalyst was found to be recyclable. 相似文献
75.
Activity coefficients of hydrochloric acid have been determined from electromotive-force measurements of cells containing mixtures of hydrochloric acid and calcium chloride at constant total ionic strengthsI=0.1, 0.5, 1.0, 2.0, and 3.0 mole-kg–1 at 298.15°K. Interpretations based on Scatchard's and Pitzer's equations indicate that Pitzer's equations probably provide a more convenient guide to the thermodynamic properties of the mixed-electrolyte solutions. Activity coefficients for calcium chloride were derived from these equations. 相似文献
76.
Two flow injection analyses (FIA) methods for the determination of diffusion coefficients in a straight single tube FIA system were developed. Based on the analytical solution of the convection-diffusion equation, linear relationships of the logarithmic values of the dispersion coefficient (D) and the half-peak width (W1/2) with the diffusion coefficient (Dm) were obtained. Experiments were designed to verify these methods. For example, for potassium hexacyanoferrate (III) a Dm value of 0.72 × 105 cm2 s−1 was found versus a literature value of 0.76 × 105 cm2 s−1 (error, 5%). For potassium hexacyanoferrate (II) a Dm value of 0.67 × 105 cm2 s−1 was obtained versus a literature value of 0.63 × 105 cm2 s−1 (error, 6%). The diffusion coefficients of some important biomedical compounds, such as dopamine, epinephrine, norepinephrine and ascorbic acid, were then determined. The values of 105 Dm/cm2 s−1 are 0.60 ± 0.03, 0.44 ± 0.02, 0.60 ± 0.01 and 0.68 ± 0.06, respectively. 相似文献
77.
The Born→Green→Yvon equation for molecular fluid has been deduced considering the orientational distribution functions. The
isotropic and anisotropic parts of the distribution function have been separated. The expressions deduced can be used in the
case of mixtures and for the non-central type of intermolecular potential energy. 相似文献
78.
Francesco Malatesta Giacomo Carrara Maria Perla Colombini Ambrogio Giacomelli 《Journal of solution chemistry》1993,22(8):733-749
The activity coefficients of Co(en)3Cl3 and K2SO4 were measured by means of a cell with ion-exchange liquid membranes following the method described in paper I. The results prove that this method is even more valuable with multicharged salts than with 1-1 electrolytes. The values obtained are precise and reliable down to dilution limits never before accessible, e.g., 4×10–5 mol-kg–1 in Co(en)3Cl3. High dilution levels are of particular importance when dealing with highly charged electrolytes since the trend at higher concentrations often leads to errors both in extrapolation to infinite dilution and in the absolute activity coefficients. As an application, the activity coefficients of [Co(en)3]2(SO4)3-suspected to be wrongly evaluated in past literature-were measured, and their values at low concentrations were actually lower than those quoted before. 相似文献
79.
Diffusion coefficients of copper sulfate-water and copper sulfate-sulfuric acid-water solutions have been determined at 25°C using conductimetric and diaphragm-cell techniques. The ternary diffusion measurements indicate that diffusion of sulfuric acid can produce large counterflows of copper sulfate and vice versa. If diffusion of copper sulfate in aqueous sulfuric acid solutions is treated as a binary process, the measured apparent diffusivities of copper sulfate can be 1 to 8% lower than the salt's true diffusivity. Equations are developed to predict transport coefficients from the concentrations and mobilities of the diffusing species. 相似文献
80.
Enthalpies of dilution of formamide, N-methylformamide, N-ethylformamide, N-propylformamide, N-butylformamide, N-pentylformamide, N,N-diethyl-formamide, N,N-dipropylformamide, N,N-dibutylformamide, and N,N-dipentyl-formamide dissolved in N,N-dimethylformamide as solvent have been measured calorimetrically at 25°C. The results are interpreted in terms of the McMillan-Mayer theory. Enthalpic interaction parameters are obtained for pairs, triplets, and in some cases, quadruplets of solute molecules. In general, the enthalpic pair interaction coefficients are negative, whereas the triplet coefficients are positive. The interaction enthalpies are positive only for N-methylformamide and formamide. The magnitudes of the enthalpic pair and triplet interaction coefficients increase with increasing number of C atoms in the N-alkyl groups. The results for the formamides presented in this paper are compared with those for corresponding acetamides published earlier. Although the trends are comparable, distinct differences are observed. The contribution of the -CH3 group at the CO side of the dialkylacetamides to the enthalpic interaction coefficients appears to be negligible. The same is true for -CH2 groups at the NH side of a number of amides and related compounds. The enthalpic pair interaction coefficients of the mono-N-alkylsubstituted formamides show a shift of about 100 J-kg-mol–2 as compared with isomeric N-alkylacetamides. This is discussed in terms of the difference in proton donating and accepting ability of several types of amide molecules. It is concluded that substitution effects should be incorporated in additivity models for these type of systems. 相似文献