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71.
The role of gas phase CH3 radicals in the oxidative coupling of CH4 over 1 wt% Sr/La2O3 is supported by the observations that (i) this is a very effective catalyst for the generation of CH3 · radicals and (ii) the concentration of CH3 · radicals increases with temperature over the range of 450 °C–800 °C. 相似文献
72.
E Aida Pea‐Ramos Youling L Xiong Guillermo E Arteaga 《Journal of the science of food and agriculture》2004,84(14):1908-1918
Whey protein isolate (WPI) was hydrolysed for 1 h using Alcalase, Protamex and Flavourzyme. Native WPI, hydrolysed WPI and two commercial WPI hydrolysates were subjected to fractionation by size exclusion chromatography. Antioxidant activity of WPI fractions was measured with a liposome‐oxidising system (50 µM FeCl3/0.1 µM ascorbate, pH 7.0). Lipid oxidation was measured as thiobarbituric acid‐reactive substances (TBARS). Gel electrophoresis and amino acid analysis were run to identify the peptide composition. The influence of amino acid composition on antioxidant activity was evaluated using multivariate analysis methods (correlation analysis, principal component analysis, multiple linear regression and discriminant analysis). TBARS assays indicated the presence of antioxidant activity in all protein fractions, including non‐hydrolysed WPI. For native and hydrolysed WPI samples the first fraction (> 45 kDa) showed a higher TBARS inhibition effect (24–27%) when compared with lower‐molecular‐weight fractions and hydrolysate mixtures. In contrast, for commercial WPI hydrolysates a higher inhibitory effect was found in most of the lower‐molecular‐weight fractions (30–55%). The ability of WPI fractions to delay lipid oxidation was found to be related to the prevalence of histidine and hydrophobic amino acids. Copyright © 2004 Society of Chemical Industry 相似文献
73.
La-OMS-2催化剂催化甲苯氧化制苯甲醛 总被引:1,自引:0,他引:1
合成了氧化锰八面体(OMS-2)分子筛,采用离子交换法和浸渍法制备了稀土金属La改性的OMS-2分子筛(La-OMS-2)催化剂,并用于甲苯液相选择性氧化制苯甲醛,考察了催化剂用量、反应温度、反应时间、氧气流量及溶剂种类对甲苯转化率和苯甲醛选择性的影响,对La-OMS-2催化剂进行了X射线衍射表征和BET比表面积测定。实验结果表明,离子交换法制备的La-OMS-2-A催化剂的活性高于浸渍法制备的La-OMS-2-B催化剂,在甲苯0.1mol、溶剂冰乙酸10mL、氧气流量60mL/min、La-OMS-2-A催化剂用量0.10g、反应温度353K、反应时间1.0h的条件下,甲苯转化率达61%,苯甲醛收率为56%。加入La对OMS-2分子筛中的MnO晶格结构产生了影响,提高了苯甲醛的收率。 相似文献
74.
英台地区天然水驱油藏的开发特点及稳产技术 总被引:2,自引:0,他引:2
陈国利 《油气地质与采收率》2003,10(6):45-47
掌握边底水运动规律,控制并利用活跃的边底水能量,是成功开发天然水驱油藏的关键。英台地区的英台、四方坨子和一棵树等三个油田均为天然水驱油藏,天然能量充足。油藏投入开发后初期含水较高,含水上升极快,造成产油量大幅度递减。针对其开发特点,适时采用大泵、电潜泵提液强采,通过大量补孔层间接替以及加密调整和扩边等稳产技术措施,确保了油藏以3%-5%的采油速度长期稳产,水驱采收率高达50%以上。 相似文献
75.
I.Z. Ismagilov R.P. Ekatpure L.T. Tsykoza E.V. Matus E.V. Rebrov M.H.J.M. de Croon M.A. Kerzhentsev J.C. Schouten 《Catalysis Today》2005,105(3-4):516-2
This paper describes the optimization of three processes applied in fabrication of a microstructured reactor for complete oxidation of volatile organic compounds. The first process involves the optimization of the electro discharge machining (EDM) method to produce a set of microchannels with a high length to diameter ratio of 100, with a standard deviation from the average diameter below 0.2%, and with a surface roughness not higher than 2.0 μm. To satisfy these criteria, fabrication of microchannels must be carried out with two machining passes in the Al51st alloy. Then, the effect of several parameters on the anodization current efficiency with respect to oxide formation was studied. The best process conditions to get a 30 μm porous alumina layer in a 0.4 M oxalic acid electrolyte, were found to be a temperature of 1 °C, an anodic current density of 5 mA/cm2, and 23 h oxidation time. At last, the resulting coatings were impregnated with an aqueous solution of copper dichromate followed by drying and calcination at 450 °C to produce active catalysts. The effect of a copper dichromate concentration, number of impregnation cycles (1 or 2), and different after-treatments on catalytic activity and stability in complete oxidation of n-butane were studied. The catalytic activity of the obtained coatings is superior to that of alumina supported pelletized catalysts even at much lower loadings of active metals. 相似文献
76.
Ahmad Nozad Golikand Elaheh Lohrasbi Mohammad Ghannadi Maragheh Mehdi Asgari 《Journal of Applied Electrochemistry》2008,38(6):869-874
The effect of carbon surface oxidation on platinum supported carbon particles (Pt/C) with nitric acid was investigated by
cyclic voltammetry, electrochemical impedance spectroscopy, polarization experiments and chronoamperometry. Cyclic voltammograms,
polarization curves and electrochemical impedance spectra showed that the treated catalyst had much larger active surface
area and higher ionic conductivity than the untreated catalyst, and provided enhanced performance for oxygen reduction. The
formation of acidic groups was examined by IR spectra. The Pt/C surface oxidation had a large effect on the performance of
a gas diffusion electrode for oxygen reduction reaction. 相似文献
77.
Anodic oxidation of mecoprop herbicide at lead dioxide 总被引:1,自引:0,他引:1
The electrochemical oxidation of an aqueous solution containing mecoprop (2-(2-methyl-4-chlorophenoxy)propionic acid) has
been studied at PbO2 anodes by cyclic voltammetry and bulk electrolysis. The influence of current density, hydrodynamic conditions, temperature
and pH on the degradation rate and current efficiency is reported. The results obtained show that the use of PbO2 leads to total mineralization of mecoprop due to the production of oxidant hydroxyl radical electrogenerated from water discharge.
The current efficiency for the electro-oxidation of mecoprop is enhanced by low current density, high recycle flow-rates and
high temperature. In contrast, the pH effect was not significant. It has also been observed that mecoprop decay kinetics follows
a pseudo-first-order reaction and the rate constant increases with rising current density. 相似文献
78.
Debasmita Das Purabi Rani Samaddar Pratik Kumar Sen Kaushik Das 《Journal of Applied Electrochemistry》2008,38(6):743-749
Galvanostatic steady state current potential measurements were carried out for oxidation of a series of aliphatic alcohols
having varying number of hydroxyl groups. The anodically deposited layer of MnO2 on platinum was used as the electrode material. The deposit was characterised by scanning electron microscopy (SEM), energy
dispersive X-ray analysis (EDAX) and electrode potential measurements. The catalytic role of MnO2 in the electro-oxidation of alcohols was indicated by the chronopotentiograms and the cyclic voltammograms. An analysis of
the electrochemical data indicated a catalytic EC mechanism in which Mn (V) is generated electrochemically and consumed chemically
in succession. Based on this and the hydrogen bonding interaction between alcoholic hydroxyl groups and MnO2 layer, a mechanism was proposed which accounts for the variation in the observed electrochemical reaction orders. Tafel behaviour
was found to be followed only approximately. Current efficiency of the electrochemical oxidation of polyols was studied. Replacement
of platinum by carbon as current collector was found to leave the electrocatalytic activity of the MnO2 deposit practically unaltered. 相似文献
79.
Teresa Łuczak 《Journal of Applied Electrochemistry》2008,38(4):469-476
The electrooxidation of phenylethanolamine (2-amino-1-phenylethanol) at a gold electrode in alkaline electrolyte has been
studied. Measurement of the differential capacitance of the electric double layer versus the electrode potential has shown
that the adsorption of phenylethanolamine at the gold-solution interface plays a significant role in the oxidation mechanism.
The effect of amine concentration, electrolyte pH and potential scan rate on the electrooxidation is analysed. 相似文献
80.
ZhangBaoji WangXieqing 《中国炼油与石油化工》2003,(3):49-52
A Ti/Si complex zeolite has been prepared. X-ray diffraction and infrared spectrometry study has shown that two structures, namely the ZSM-5 and MCM-41, exist in the sample. BET tests have revealed that the complex zeolite contains regular mesopores of 2.6 nm. Ultraviolet spectrometry analysis has shown that the Ti species exist in the zeolite skeleton in the form of tetra-coordinate valence. The Ti/Si complex zeolite (TS-1/Ti-MCM-41) has apparently improved catalytic activity with respect to the macromolecular organic compound oxidation as compared to individual components of either Ti or Si containing zeolites (TS-1 and Ti-MCM-41). 相似文献