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81.
82.
A new Ag/Al2O3 catalyst for removing NOx in lean exhaust gas was developed. Oxidized Ag/Al2O3 catalyst is highly active for reduction of NOx with ethanol and propene, whereas reduced Ag/Al2O3 catalyst is less active for these reactions. Selectivity to N2 is also high on the oxidized Ag/Al2O3 compared to that on the reduced Ag/Al2O3. XRD and SEM studies of these two types of Ag catalysts suggest that oxidation induces an interaction between Ag and the
support, where the particles are grown in large size. In contrast, the metallic Ag particles are finely dispersed by the reduction
process. Although dispersion of Ag particles is decreased by the oxidation process, the catalytic activity is increased. This
suggests that the Ag-alumina sites created in the high temperature oxidizing environment are active in catalytic reduction
of NOx.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
83.
The hexane-soluble fractions of hydroliquefied products from three Yallourn brown coal lithotypes have been separated into five fractions by combined silica-alumina packed column chromatography. Analyses of various fractions by g.c.-m.s. permitted the identification of ≈50 components in the saturate fraction and 40 components in the diaromatic fraction, together with 30 components in the monoaromatics. The components identified were quite similar among hexane-soluble portions of all three lithotypes. A marked predominance of even carbon number alkane (C23-C29) was observed in the hydrocarbon fractions from pale lithotype over , and medium light lithotype over both pure ZnCl2 and . However, medium dark lithotype over both melt catalysts produced a saturate fraction with an odd carbon number(C22-C28) preference. Based on spectral methods, Soxhlet extracts obtained from untreated lithotypes (hexane and benzene solubles) were characterized as complex mixtures of higher molecular weight(300–1000) aliphatic hydrocarbons, which were supposed to be a precursor of the saturates produced from the corresponding lithotype in the catalytic hydroliquefaction. 相似文献
84.
Hiromi Yoshida Mikiko Tatsumi Goro Kajimoto 《Journal of the American Oil Chemists' Society》1991,68(8):566-570
Effects of microwave heating on the oxidative stability ofd-tocopherols were studied in relation to the production of fatty acids in oils. During microwave heating, the stability of
tocopherols decreased in the orderδ>β>γ>α. This order did not depend on the types of ethyl esters of fatty acids or oils present. But, the shorter the chainlength
and the lower the degree of unsaturation of the fatty acid ethyl esters, the greater was the reduction in amount of individual
tocopherols. A similar tendency was observed when tocopherol-stripped vegetable oils, with equimolar mixtures of tocopherols
added, were treated under the same conditions. The reduction in tocopherols became greater with increasing levels of free
fatty acids. 相似文献
85.
Yoshihiro Kubota Yusuke Nishizaki Hisanori Ikeya Masami Saeki Tetsunari Hida Sachiko Kawazu Michitaka Yoshida Hidekazu Fujii Yoshihiro Sugi 《Microporous and mesoporous materials》2004,70(1-3):135-149
Two types of organic–inorganic hybrid base catalysts are prepared. Organic-functionalized molecular sieves (OFMSs), particularly “amine-immobilized porous silicates”, are designed based on common idea to immobilize catalytic active sites on silicate surface. Silicate–organic composite materials (SOCMs), such as “ordered porous silicate–quaternary ammonium composite materials”, are the precursors of ordered porous silicates obtained during the synthesis. Both the OFMS and the SOCM are used as the catalysts for Knoevenagel condensation. Among the OFMSs, there is clear tendency that the use of molecular sieve with larger pore volume and/or surface area gives the product in higher yield. Aminopropylsilyl (AP)-functionalized mesoporous silicates such as AP-MCM-41 gives the product in high yield under mild conditions. No loss of activity is observed after repeated use for three times. The SOCMs are also active for the same reaction. The precursors of the mesoporous silicates are more active than those of microporous silicates. This material can be repeatedly used without significant loss of activity. High activity is not due to the leached species. The active sites of the SOCM catalysts are considered to be SiO− moieties located on the pore-mouth. Activity of the SOCM increases when the reaction is carried out without solvent, whereas decrease in activity of the OFMS is observed in the solvent-free system. 相似文献
86.
The rate of evaporation of monodisperse water droplets was first evaluated by solving numerically the modified Maxwell equation, assuming the cellular model for a droplet clouds. The results are discussed in comparison with those for a single isolated droplet, which can be obtained analytically. The critical conditions for the droplet cloud to be stable are then evaluated as a function of droplet number concentration, droplet size and initial conditions of the surrounding air. Secondly, the equilibrated system, where a water droplet cloud is steadily mixed with unsaturated air, was analysed on the basis of enthalpy and material balance of the system to evaluate the total volume change of the droplets. Some of these analyses were verified by experiment, using an ultramicroscopic technique which is useful for droplet size analysis. 相似文献
87.
Tetsuto Kanzaki Yo Ishikawa Nobuhiro Morisaki Kohji Shirai Yasushi Saito Sho Yoshida 《Lipids》1987,22(10):704-710
Studies were done on changes in phospholipid content and fatty acid composition of phospholipids and on the role of the acylation
pathway in synthesis of phospholipids in the development of abnormal fatty acid composition in the glomeruli of rats 2 and
10 mo after induction of diabetes with streptozotocin. The proportions of individual phospholipids in the glomeruli of rats
were not changed 2 mo after induction of diabetes, but the proportion of phosphatidylethanolamine (PE) decreased and that
of sphingomyelin increased 10 mo after induction of diabetes. In contrast, in liver the proportion of PE was increased and
that of phosphatidylcholine was decreased. These results showed that changes of individual phospholipids in glomeruli were
time-dependent and tissue-specific. Two mo after induction of diabetes, the main change in the phospholipid fatty acid composition
of diabetic glomeruli was a decrease in arachidonic acid (AA); the main change in serum free fatty acids (FFA) was an increase
in linoleic acid (LA) and a decrease in AA. Ten mo after induction of diabetes, the main changes in the phospholipid fatty
acid composition of glomeruli were an increase in LA and a decrease in AA; the main change of the serum FFA composition was
a decrease in AA. Thus, the fatty acid composition of glomerular phospholipids was not directly correlated to that of the
serum in diabetic rats. Acyl-CoA synthetase and acyltransferase activities increased in diabetic glomeruli with either AA
or LA as substrate, but activity toward LA increased more at 2 mo after induction of diabetes. Acyl-CoA synthetase activity
increased in diabetic glomeruli with LA as substrate, but that did not change with AA as substrate at 10 mo after induction
of diabetes. Furthermore, acyltransferase activity decreased in diabetic glomeruli with AA as substrate, although that did
not change with LA as substrate at 10 mo after induction of diabetes. 相似文献
88.
The free‐radical graft polymerization of vinyl acetate onto nonporous silica particles was studied experimentally. The grafting procedure consisted of surface activation with vinyltrimethoxysilane, followed by free‐radical graft polymerization of vinyl acetate in ethyl acetate with 2,2′‐azobis(2,4‐dimethylpentanenitrile) initiator. Initial monomer concentration was varied from 10 to 40% by volume and the reaction was spanned from 50 to 70°C. The resulting grafted polymer, which was stable over a wide range of pH levels, consisted of polymer chains that are terminally and covalently bonded to the silica substrate. The experimental polymerization rate order, with respect to monomer concentration, ranged from 1.61 to 2.00, consistent with the kinetic order for the high polymerization regime. The corresponding rate order for polymer grafting varied from 1.24 to 1.43. The polymer graft yield increased with both initial monomer concentration and reaction temperature, and the polymer‐grafted surface became more hydrophobic with increasing polymer graft yield. The present study suggests that a denser grafted polymer phase of shorter chains was created upon increasing temperature. On the other hand, both polymer chain length and polymer graft density increased with initial monomer concentration. Atomic force microscopy–determined topology of the polymer‐grafted surface revealed a distribution of surface clusters and surface elevations consistent with the expected broad molecular‐weight distribution for free‐radical polymerization. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 300–310, 2003 相似文献
89.
Tsuyoshi Hagio Kazuo Kobayashi Hisayoshi Yoshida Hiroaki Yasunaga Hiroshi Nishikawa 《Journal of the American Ceramic Society》1989,72(8):1482-1484
Pressureless sintering of hexagonal boron nitride (BN) was performed using a powder activated by mechano-chemical treatments. Physical properties of the sintered BN bodies depend on the type of starting powder and the conditions of the treatments. The BN body, which was obtained at 2000°C using an appropriate activated powder, was 99 wt% pure and was excellent in mechanical and physical properties, in spite of its low density (1.64 g/cm3 ). 相似文献
90.
Jinhua Chen Upita Septiani Masaharu Asano Yasunari Maekawa Hitoshi Kubota Masaru Yoshida 《应用聚合物科学杂志》2007,103(3):1966-1972
In this study the fluoropolymers, poly(ethylene‐co‐tetrafluoroethylene) (ETFE) and poly(vinylidene fluoride) (PVDF) films, together with the radiation‐induced crosslinked polytetrafluoroethylene (cPTFE) film were compared on the basis of their preparation and properties of radiation‐grafted polymer electrolyte membranes. The polymer electrolyte membranes were prepared by radiation grafting of styrene into the base films and subsequent sulfonation. The proton conductivity and chemical stability of the three types of membranes with a similar ion exchange capacity (IEC) near 1.0 mmol/g were investigated and are discussed in detail. Although the ETFE‐based polymer electrolyte membrane was relatively more stable, its proton conductivity was lower than those of the PVDF‐ and cPTFE‐based membranes. On the other hand, the cPTFE‐based membrane showed a significantly higher proton conductivity, but its chemical stability was shorter than that of the ETFE‐based membrane. It is considered that the difference in the preparation and properties of the polymer electrolyte membranes was due to the difference in the degree of crystallinity as well as in the chemical structure of the fluoropolymer base films. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 1966–1972, 2007 相似文献