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991.
Propylene epoxidation over Ti/MCM-41 catalysts prepared by chemical vapor deposition 总被引:3,自引:0,他引:3
Ti-containing mesoporous catalysts were prepared by chemical vapor deposition (CVD) of TiCl4 on silica MCM-41 in the 700–900 °C temperature range. These samples were characterized (with XRD, ICP, nitrogen adsorption, FT-IR, ESCA, and TEM) and evaluated for the epoxidation of propylene with two alkyl hydroperoxides. The increase of CVD temperature resulted in the decrease of titanium content, catalyst hydroxyl population, crystallinity, and surface area. Catalyst selectivity to the desired product – propylene oxide – was highly sensitive to the deposition temperature. The best Ti/MCM-41 catalyst was prepared at the temperature of 800 °C, which had the maximum propylene oxide yield of 94.3%. 相似文献
992.
993.
Fiber-bundle push-out, single-fiber push-in, and single-fiber push-out tests were conducted in order to examine the applicability of these methods for determining the interfacial shear strength of carbon-carbon composites. The fiber-bundle push-out test resulted mostly in fractures along the fiber/matrix interface but created a small amount of fractures in the matrix. Hence, the evaluated strength was regarded as an approximate value. In order to precisely evaluate the interfacial strength, push-in and push-out tests for a single fiber were performed using a micro-Vickers indentation tester. In these tests, the load has to be placed within a target fiber, and the indentation should not extend to the matrix. This condition restricted the load that could be applied to a carbon fiber. Within this limit, a single carbon fiber could not be pushed-in. For the sake of load reduction, single-fiber push-out tests were conducted using thin specimens. The thickness appropriate for a single-fiber push-out specimen was estimated based on the interfacial shear strength obtained by the bundle push-out tests. Below this thickness, single-fiber push-out tests could be successfully performed. 相似文献
994.
John F. Quinn Author Vitae Author Vitae Leonie Barner Author Vitae Author Vitae 《Polymer》2007,48(22):6467-6480
Ionizing radiation, such as γ, ultraviolet, microwave and X-ray radiation, has long been used in polymer chemistry as a means of initiating polymerization, crosslinking gels and decomposing particular polymer components. More recently, ionizing radiation has found application in tandem with living radical polymerization to form novel polymeric materials with defined molecular weight and narrow molecular weight distribution. In particular, γ-rays and ultraviolet light both have shown promise as sources of initiation in reversible addition-fragmentation chain transfer (RAFT) polymerization. The ability to apply these sources of initiation at low temperatures is useful in applications where elevated temperature is likely to be detrimental to the system, for instance, in preparing protein-polymer conjugates. Similarly, the use of these initiating sources at low temperature is particularly suitable for some monomers, such as allyl compounds, which have not been synthesized using any other living radical approach. The current review examines the development of ionizing radiation as a tool in RAFT polymerization, with particular reference to the elucidation of the polymerization mechanism, the synthesis of high functionality polymers and probing the kinetic parameters of the RAFT process. 相似文献
995.
M. Pérez-Luna A. Cosultchi J. A. Toledo-Antonio C. Angeles-Chavez E. M. Arce-Estrada 《Catalysis Letters》2006,107(1-2):103-110
Three Ni/ZrO2–SO4=/Al2O3 catalysts with different concentrations of platinum (0.2, 0.3 and 0.4 wt%) were prepare and tested for n-butane isomerization reaction at 338 K, in absence and in presence of hydrogen. The results shown that, at low temperature,
platinum contributes to the olefin or butyl ion formation and the reaction follows a bimolecular pathway. However, when the
reaction occurs in the presence of hydrogen, the formation of butyl ions is inhibited. The main feature of platinum addition
is the stabilization of the catalytic activity, which is indicated by the slow deactivation constants compared to that of
the unpromoted catalyst. 相似文献
996.
Recent studies of self-condensation and co-condensation of melamine-formaldehyde resins; cure at low temperatures 总被引:1,自引:0,他引:1
Self-condensation: recent research on the chemical pathways by which alcoholated melamine-formaldehyde (MF) resins react with themselves and on the product structures is summarized. Model compound studies suggest that
bridges are less stable than widely thought unless they are in hexahydro-1,3,5-triazine ring structures. In acyclic structures they are probably less stable than
bridges. Co-condensation: studies of how the composition of MF resins influences the rates of reaction with poly(ol) co-reactant show that MF resins that contain very low levels of
and/or
functionality are quite reactive. Reactivities of a variety of poly(ester) and acrylic coreactants were studied. By combining reactive MF resins with reactive co-reactants one can formulate high solids enamels that cure by co-condensation in 30 min at 50 to 65 °C with 0.5 parts per hundred (phr) of p-toluenesulfonic acid (p-TSA) catalyst. Cure at 25 °C appears feasible with higher catalyst levels. 相似文献
997.
Walter Brockmann 《The Journal of Adhesion》1989,29(1):53-61
Adequate adhesion between metals and polymers is primarily the result of chemical bonds in the boundary layer. This region, however, is subject to degradation by moisture. Three modes of deterioration are observed. The first is a largely reversible weakening effect in the polymer layer near the metal oxide surface. The structure of this layer differs from that of the bulk and is influenced by the chemical and physical properties of the surface. The second is a slow transformation of the oxide by hydration and a diffusion of oxide constituents into the polymer. This process is irreversible and is influenced by the state of the surface and chemical properties of the polymer. The third is a fast deterioration of the oxide by primary corrosion usually initiating at an unprotected edge but occasionally arising within the body of a joint. 相似文献
998.
999.
Hongwu Xu Alexandra Navrotsky M. Lou Balmer Yali Su 《Journal of the American Ceramic Society》2002,85(5):1235-1242
The crystal structures for a suite of substituted pollucites with the compositions CsTi x Al1– x Si2 O6+0.5 x , 0 ≤ x ≤ 1, have been determined from Rietveld analysis of powder synchrotron XRD data. Our results indicate that the pollucite end member (CsAlSi2 O6 ) has a tetragonal structure (space group I 41 / a ), whereas all other compositions are cubic (space group Ia 3 d ). The increased symmetry for the titanium-substituted structures is presumably due to the incorporation of additional O2− anions (needed for compensating the charge imbalance between Ti4+ and Al3+ ), which effectively holds open the expanded cubic framework. In situ cooling experiments of the substituted phase CsTi0.1 Al0.9 Si2 O6.05 reveal a displacive transformation to the tetragonal structure at ∼230 K. This transformation is tricritical in nature and is analogous to the tetragonal-to-cubic transition in pollucite on heating. 相似文献
1000.
William R. Chase Muraleedharan G. Nair Alan R. Putnam Saroj K. Mishra 《Journal of chemical ecology》1991,17(8):1575-1584
Acinetobacter calcoaceticus, a gram-negative bacterium isolated from field soil, was found to be responsible for the biotransformation of 2(3H)-benzoxazolinone (BOA) to 2,2-oxo-1,1-azobenzene (AZOB). Experiments were conducted to evaluate the transformation of BOA to AZOB by this microbe in sterile and nonsterile soil. Transformation studies with soils inoculated withA. calcoaceticus indicated that the production of AZOB increased linearly with the concentration of BOA in sterile soil and showed a quadratic trend in nonsterile soils. This also indicated that all soil types studied for the transformation experiments might containA. calcoaceticus capable of the conversion of benzoxazolinones. 相似文献