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61.
Sn-incorporated folded sheets mesoporous materials (Sn-FSM-16) with various contents of Sn were synthesized by using a mixture of water glass, SnCl4 and NaOH as starting materials. Hexadecyltrimethyl-ammonium chloride (surfactant) was used to intercalate into the layered silicate. The reaction process was followed by measurements of XRD patterns of intermediates. The Sn-FSM-16 was formed via the following mechanism: (1) layered silicates such as - - and -Na2Si2O5 were formed as intermediates by the calcination of the mixture of the starting materials; (2) the surfactant was intercalated into the layered silicates; (3) the surfactant-silicate complex with hexagonal structure was obtained as a precursor of Sn-FSM-16; (4) the precursor was calcined to decompose the surfactant in the interlayer and was changed to Sn-FSM-16. The structural aspect of Sn in Sn-FSM-16 was studied by XPS profiles of Sn 3d
5/2 and Si2p, 29 Si MAS NMR and FTIR. The content of Sn in Sn-FSM increased with increasing concentrations of both Sn and NaOH in the starting materials. The surface area of Sn-FSM-16 decreased with an increase of Sn content in Sn-FSM (1160–620 m2/g). 相似文献
62.
Kazuhiko Takeuchi Taka-aki Hanaoka Takehiko Matsuzaki Yoshihiro Sugi Shigeto Ogasawara Yoshimoto Abe Takahisa Misono 《Catalysis Today》1994,20(3):423-435
An in situ diffuse reflectance FT-IR technique was employed to investigate the active surface species and the reaction mechanism of the oxygenate formation in the vapor phase hydroformylation of ethene on Co/SiO2 promoted with various noble metals such as Ir, Rh, Pt, Re, Ru, and Pd. Co(A)/SiO2 and Ir(CO)/SiO2 which were derived from cobalt(II) acetate and Ir4(CO)12, respectively, were quite inactive in the reaction, and showed only quite small peaks of adsorbed CO under the conditions of 1.1 MPa of C2H4/CO/H2 at 298 K. In contrast, Co(A)-Ir(CO)/SiO2, which were very active in the reaction, exhibited strong absorption bands of linear and bridged CO species. At 423–463 K, propanal adsorbed on the catalyst and acyl species which is suggested as the intermediate for the formation of propanal were also observed on this catalyst. By exposing CO preadsorbed on this catalyst to C2H4/H2 at 289 K and 0.1 MPa, the intensity of the linear CO band decreased, and the bands of propanal and acyl species emerged simultaneously, whereas that of the bridged CO band remained constant after the initial drop. These results suggested that the oxygenates are formed via the CO insertion into adsorbed ethyl species, and linear CO species plays a major role in the CO insertion on these noble metal-promoted cobalt catalysts. 相似文献
63.
Masayuki Nogami Yoshihiro Abe Ayako Kato 《Journal of the American Ceramic Society》1995,78(4):1066-1070
Silica glasses doped with small-sized CdSx -Se1-x crystals were prepared by the sol-gel method. Gels synthesized by the hydrolysis of Si(OC2 H5 )4 , in the presence of CdSeO4 with NH4 SCN dissolved in HNO3 or NH4 OH, were heated in H2 -N2 atmosphere. The pH value of solutions for CdSeO4 and NH4 SCN primarily determined the fraction of anions in CdSx Se1-x crystals. The anion content in crystals was dependent on the pH value of the solvent and/or heat-treatment temperature, and the sulfur fraction changed from 0.1 to 0.6. The optical absorption spectra were red-shifted as the selenium content and the crystal size increased, and the emission spectra showed a sharp band near the absorption edge position and a broad tail extending into the long wavelength. The optical band gap energies increased reciprocally proportional to the square of the crystal size. 相似文献
64.
N,N'- Unsymmetrical dialkyl-3,4:9,10-perylenebis(dicarboximide)s (in which alkyl = methyl, ethyl, propyl, butyl, isobutyl, pentyl, hexyl and octyl) were prepared by the condensation of N-alkyl-3,4:9,10-perylene-tetracarboxylic monoanhydride monoimide with the appropriate alkyl-amines. The properties of these derivatives as pigments were tested and their thermal stability measured. 相似文献
65.
羧甲基纤维素阳离子化衍生物的研究现状 总被引:3,自引:0,他引:3
羧甲基纤维素阳离子化改性是制备性能优良的天然两性高分子的重要方法之一。文章综述了迄今为止羧甲基纤维素阳离子化改性所用的阳离子单体的主要类型及其接枝的若干主要途径,其中包括自由基型接枝共聚、高分子侧基反应、聚合后功能化等三大类。 相似文献
66.
聚合物熔体在圆锥短口模的挤出胀大方程 总被引:3,自引:1,他引:3
深入讨论了聚合物熔体在不同长径比、不同角度圆锥短口模的挤出胀大现象及机理,利用生产用挤出机进行不同角度的圆锥短口模实验。结果表明,圆锥短口模挤出过程中,熔体在收敛流道受到拉伸流变,导致强烈的入口弹性效应,表现为熔体在短口模挤出时显著的挤出胀大。理论和实验研究结果进一步表明不同圆锥口模入口角对实验材料表现出有不同的挤出胀大值。 相似文献
67.
68.
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
69.
Carbon materials are often used as catalyst supports, and for catalysts in electrodes of a polymer electrolyte fuel cell, carbon black has been used. Recently, it was found, however, that activated carbon could replace carbon black and besides, significantly improve the activity of the electrode catalyst layer for oxygen reduction. In the present study, to optimize the pore structure of activated carbon for further activity improvement, the influence of the pore structure on the activity was investigated using activated carbon of various specific surface areas and mean pore diameters. A catalyst layer was formed from activated carbon loaded with platinum and a polymer electrolyte. The activity of the layer was measured in an oxygen-saturated perchloric acid solution, supporting the layer on a rotating glassy carbon disk electrode. We found that increases in the specific surface area and mean pore diameter increased the activity and that the latter was more effective than the former mainly due to the enhanced mass-transfer in the pores; the catalyst layer formed from activated carbon with the largest mean pore diameter was the most active. Unless pores excessively develop and lose connections between particles, a large pore diameter is therefore desired for the fuel cell electrodes. 相似文献
70.