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101.
Keiji Kunimatsu Takahiro Senzaki Minoru Tsushima Masatoshi Osawa 《Electrochimica acta》2007,52(18):5715-5724
Hydrogen evolution reaction (HER) on a polycrystalline Pt electrode has been investigated in Ar-purged acids by surface-enhanced infrared absorption spectroscopy and electrochemical kinetic analysis (Tafel plot). A vibrational mode characteristic to H atom adsorbed at atop sites (terminal H) was observed at 2080-2095 cm−1. This band appears at 0.1 V (RHE) and grows at more negative potentials in parallel to the increase in hydrogen evolution current. Good signal-to-noise ratio of the spectra enabled us to establish the quantitative relation between the band intensity (equivalently, coverage) of terminal H and the kinetics of HER, from which we conclude that terminal H atom is the reaction intermediate in HER and the recombination of two terminal H atoms is the rate-determining step. The quantitative analysis of the infrared data also revealed that the adsorption of terminal H follows the Frumkin isotherm with repulsive interaction. 相似文献
102.
Poly(acrylamide‐co‐maleic acid) [P(AAm/MA)] hydrogels, with various compositions, were prepared from ternary mixtures of acrylamide (AAm)/maleic acid (MA)/water by using 60Co γ‐rays. The effect of composition of these hydrogels, on the competitive removal of Pb2+, Cd2+, and Zn2+ ions from aqueous solution, was investigated. The hydrogel compositions and their adsorption behaviors were determined by use of differential pulse polarography, a very sensitive electroanalytical technique. It was observed that the external stimuli of pH, temperature, and ionic strength have an important role on the adsorption. The increments of MA content in P(AAm/MA) hydrogels caused a significant increase in the adsorption these ions. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 2401–2406, 2004 相似文献
103.
The adsorption of cobalt phthalocyanine dye onto activated carbon in a continuous stirred tank adsorber was studied. The variables investigated were: adsorbent mass, adsorbent particle size and fluid flowrate. Several models based on film, pore and surface diffusion were constructed and fitted to the experimental data. Experimental results showed: (i) the increasing importance of the film mass transfer resistance for increasing adsorbent loads; (ii) the increasing importance of the surface diffusion mechanism for increasing adsorbent loads; and (iii) the better discrimination among different models for higher adsorbent loads and lower flowrate. 相似文献
104.
Laiyuan Chen Liwu Lin Zhusheng Xu Tao Zhang Dongbai Liang Qin Xin Pinliang Ying 《Catalysis Letters》1995,35(3-4):245-258
Infrared investigations on the interaction of methane with silica, aluminas (, and ) and HZSM-5 zeolite have been carried out. At low temperature (173 K), methane adsorption was observed over these oxides and HZSM-5 zeolite. Our findings featured that the infrared inactive
1 band (2917 cm–1) of a gaseous methane molecule became active and shifted to lower frequencies (2900 and 2890 cm–1) when it adsorbed on the surfaces of these adsorbents. Our results also demonstrate that hydroxyl groups played a very important role in methane adsorption over the acidic oxides and the HZSM-5 zeolite. When interaction between the hydroxyl groups and methane took place, the band shift of the hydroxyl groups varied with different oxides. The strength of the interaction decreased according to the following sequence, Si-OH-Al>Al-OH>Si-OH, which is in accordance with the order of their acidities. At higher temperatures, methane interacted quite differently with various oxides and HZSM-5 zeolite. It has been observed that the hydroxyl groups of silica, -alumina and HZSM-5 zeolite could exchange with CD4 at temperatures higher than 773K, while those on -alumina could exchange at a temperature as low as 573 K. Another interesting observation was the formation of formate species over Al2O3 (both and ) at temperatures higher than 473 K. The formate species would decompose to CO2, or produce carbonate at much higher temperatures. Formation of formate species was not observed over silica and HZSM-5 under similar conditions, -Al2O3 did not adsorb or react with methane in any case. 相似文献
105.
微波法制备的有机膨润土及吸附性能研究 总被引:7,自引:0,他引:7
研究了利用微波制备双阳型有机膨润土的适宜条件,对微波法制备有机膨润土的机理进行了分析,并与常规法合成的有机膨润土在结构与吸附性能方面进行了对比。结果表明,微波法制备双阳型有机膨润土的适宜条件为两种阳离子型表面活性剂总用量为100CEC,微波辐照能量210J/mL。与常规湿法的相比,有机膨润土的层间距、有机碳含量有所提高,对染料的去除率有较大提高。 相似文献
106.
Several investigations have been carried out on Cu/ZnO catalysts by employing extended Xray absorption fine structure (EXAFS) and Xray photoelectron spectroscopy (XPS). EXAFS investigations of Cu/ZnO catalysts subjected to hydrogen reduction show the presence of Cu1+ species and Cu microclusters. The proportion of Cu1+ depends on the rate of increase of the reduction temperature and on the amount of alumina added. An XPS study of the interaction of CO with model Cu/ZnO catalysts prepared in situ in the electron spectrometer shows the formation of CO2
-, CO3
2- and C2O4
2- species, their proportion relative to CO increasing with the Cu1+/Cu0 ratio. A study of the interaction of CH3OH with Cu clusters deposited on ZnO films reveals reversible molecular adsorption and the formation of CH3O on clean Cu clusters. If the Cu clusters are pretreated with oxygen, however, both CH3O and HCOO- species are produced. Model Cu/ZnO catalyst surfaces containing both Cu1+ and Cu0 species show interesting oxidation properties. On a Cu0-rich catalyst surface, only the CH3O species is formed on interaction with CH3OH. On a Cu1+rich surface, the HCOO- ion is the predominant species. 相似文献
107.
超高交联树脂吸附对硝基苯乙酮和对硝基苯甲酸的研究 总被引:1,自引:0,他引:1
研究了NDA-150、NDA-99、NDA-88、Amberlite XAD-4.4种吸附树脂对对硝基苯乙酮和对硝基苯甲酸的静态吸附行为。结果表明NDA—150树脂对硝基化合物的吸附效果较好。并研究NDA-150树脂的动态吸附和脱附行为.结果显示:NDA-150树脂对对硝基苯甲酸的吸附容量为2.32mmol/g干树脂,对对硝基苯乙酮的吸附容量为3.06mmol/g干树脂。NDA—150树脂易于脱附,吸附对硝基苯甲酸后.用2%NaOH:乙醇(体积比1:1)作脱附剂,温度313K;吸附对硝基苯乙酮后,用甲醇作脱附剂,温度333K,体积6BV,脱附率均接近100%。 相似文献
108.
For Tanzanian soils dominant in hydrous oxides of iron and amorphous ferri-alumino silicate, a 48-hour (hr) mixing period with the sulphate (SO4) solution was adequate for a near-equilibrium condition. Although differing in their SO4 sorption capacity, all the soils sorbed SO4 at or beyond 1µg ml–1 sulphur (S) concentration in the supernatant. Hydroxyl (OH) ions were displaced during SO4 sorption as indicated by a significant positive correlation between the amount of sorbed SO4 and the difference in pH values determined in 0.1N K2 SO4 and 0.1N KCl, i.e. the dpH values.In a greenhouse experiment, alfalfa was grown on eight soils at six adjusted S concentrations. Sulphur deficiency symptoms appeared in the control pots of those soils which were low in native sorbed SO4, SO4 sorption capacity and initial soil solution S concentration. Sulphur fertilization increased dry matter (DM) yield as well as response to applied S. The external S concentration, i.e. adjusted S concentration required for 95% of the maximum DM yield, ranged from 0.8 to 8.2µg S ml–1 with values less than 2.0 on most of the soils. The external S concentration decreased hyperbolically as the SO4 sorption capacity of the soils increased. The total amount of fertilizer S required to obtain the external S concentration in solution, and at the same time satisfy the SO4 sorption capacity of the soil at the external S concentration (determined from the sorption isotherm) was defined as the external S requirement for the specified yield level of alfalfa. The external S requirement for 95% of the maximum yield of alfalfa varied from soil to soil due to differences in their capacity and intensity for S nutrition.Part of a thesis by the senior author for the MSc (Agric) degree of the University of Dar es Salaam 相似文献
109.
110.
J. F. Toro-Vazquez Alejandro Rocha-Uribe 《Journal of the American Oil Chemists' Society》1993,70(6):589-594
The adsorption of peroxides, unsaturated carbonyls, free fatty acids and carotenoids from unrefined sesame oil on vegetable
carbon (5%, w/w) in a miscella system was studied. Three different solvent conditions (hexane/ethanol, 100:0, 95:5 and 75:25,
vol/vol), combined in a factorial design with five levels of solvent (0, 10, 20, 30 and 40%, w/w), were used to develop the
miscella. Equilibrium adsorption was not achieved during the 100 min of adsorption, mainly because the oil components were
involved in oxidation reactions during the adsorption process. However, for a given solvent concentration, adsorption of the
oil components showed a significant linear regression on their respective initial concentration in the miscella (Ci). Peroxides and carbonyls showed, at all solvent levels investigated, an affinity for the carbon more independent of their
Ci than free fatty acids and carotenoids. In general, at the same Ci, a higher adsorption was achieved as solvent concentration increased. The results indicated that free fatty acid adsorption
may depend on competitive adsorption based on molecule hydrophobicity. However, in spite of the higher hydrophobicity of carotenoids,
compared with free fatty acids, they might not be competing for the same adsorbing sites. Ethanol showed a prooxidant effect
that increased peroxide production during adsorption but did not affect the reaction involved in carbonyl production. 相似文献