全文获取类型
收费全文 | 24426篇 |
免费 | 2393篇 |
国内免费 | 1290篇 |
专业分类
电工技术 | 330篇 |
综合类 | 1366篇 |
化学工业 | 11874篇 |
金属工艺 | 2646篇 |
机械仪表 | 402篇 |
建筑科学 | 307篇 |
矿业工程 | 554篇 |
能源动力 | 852篇 |
轻工业 | 1590篇 |
水利工程 | 40篇 |
石油天然气 | 776篇 |
武器工业 | 165篇 |
无线电 | 686篇 |
一般工业技术 | 2737篇 |
冶金工业 | 3266篇 |
原子能技术 | 312篇 |
自动化技术 | 206篇 |
出版年
2024年 | 86篇 |
2023年 | 608篇 |
2022年 | 833篇 |
2021年 | 881篇 |
2020年 | 904篇 |
2019年 | 842篇 |
2018年 | 843篇 |
2017年 | 1001篇 |
2016年 | 924篇 |
2015年 | 816篇 |
2014年 | 1172篇 |
2013年 | 1526篇 |
2012年 | 1542篇 |
2011年 | 1517篇 |
2010年 | 1164篇 |
2009年 | 1318篇 |
2008年 | 1003篇 |
2007年 | 1428篇 |
2006年 | 1312篇 |
2005年 | 1086篇 |
2004年 | 1021篇 |
2003年 | 964篇 |
2002年 | 782篇 |
2001年 | 659篇 |
2000年 | 608篇 |
1999年 | 494篇 |
1998年 | 374篇 |
1997年 | 346篇 |
1996年 | 291篇 |
1995年 | 246篇 |
1994年 | 238篇 |
1993年 | 184篇 |
1992年 | 183篇 |
1991年 | 190篇 |
1990年 | 166篇 |
1989年 | 140篇 |
1988年 | 56篇 |
1987年 | 48篇 |
1986年 | 37篇 |
1985年 | 65篇 |
1984年 | 59篇 |
1983年 | 36篇 |
1982年 | 42篇 |
1981年 | 11篇 |
1980年 | 12篇 |
1979年 | 12篇 |
1978年 | 7篇 |
1976年 | 7篇 |
1975年 | 5篇 |
1951年 | 13篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
61.
62.
63.
V. V. Skorokhod M. B. Shtern A. V. Kuz’mov A. V. Ragulya 《Powder Metallurgy and Metal Ceramics》2006,45(5-6):221-225
A study has been made on the effects of loading scheme and conditions restricting macroscopic strain on the work-hardening
kinetics and strain accumulation in the solid state in sintering materials with bimodal pore size distributions. Active loading
intensifies the reduction in the small pores. The greatest effect comes from combining sintering with hydrostatic compression.
At the same time, kinematic constraints (partial or complete adhesion in surfaces) substantially retards the shrinkage of
large pores, which means that the porous structure can be controlled.
__________
Translated from Poroshkovaya Metallurgiya, Nos. 5–6(449), pp. 10–15, May–June, 2006. 相似文献
64.
A kinetic study on simultaneous interpenetrating polymer network formation of epoxy resin based on diglycidyl ether of Bisphenol A (DGEBA) and unsaturated polyester (UP) was performed by means of differential scanning calorimetry (DSC). Isothermal DSC characterizations of neat resins and their mixture (in a weight ratio of 50/50) were performed at different temperatures. Dynamic DSC characterization of the systems were performed at three different heating rates. A lower total heat of reaction developed during simultaneous polymerization in dynamic DSC tests was found, compared to the total heats developed during pure resins network formation. This phenomenon can be interpreted as an effect of network interlock that could not be compensated for completely by an increase in curing temperature. The kinetics of the reactions was described by empirical models. The DGEBA, in a 50/50 UP/DGEBA blend, indicated a higher rate constant than the pure DGEBA. The obtained results suggests that the hydroxyl end group of UP in the blend provided a favorably catalytic environment for the DGEBA cure. The results are in good agreement with the literature data. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2689–2698, 2002 相似文献
65.
Athanasios Eftaxias Josep Font Agusti Fortuny Azael Fabregat Frank Stüber 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2005,80(6):677-687
The wet air oxidation of phenol over a commercial active carbon catalyst was studied in a trickle bed reactor (TBR) in the temperature and oxygen partial pressure ranges of 120–160 °C and 0.1–0.2 MPa, respectively. The performance of the active carbon was compared in terms of phenol and COD destruction. The weight change of active carbon due to reaction was also measured. Finally, oxic phenol adsorption isotherms were assessed in batch conditions at 25, 125 and 160 °C. In order to use the conversion data obtained from the TBR for a kinetic study, special care was taken to check the kinetic control in the TBR experiments. Several kinetic models including power law or Langmuir–Hinshelwood expressions were considered to describe the catalytic oxidation of phenol over active carbon. The simple power law model with first order dependence on both phenol and oxygen concentration predicted satisfactorily the experimental data not only over the entire range of operating conditions studied, but also outside its validity range. Copyright © 2005 Society of Chemical Industry 相似文献
66.
67.
Maciej Winiewski Artur Jakubiak Jan Szymanowski 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》1995,63(3):209-214
Decyl isonicotiniate and decyl nicotiniate permit a rapid extraction of palladium(II) from its hydrochloride solutions. Decyl picoliniate is not a suitable extractant. 4-Octylphenylamine can act as a phase transfer catalyst when its concentration in the organic phase is at least 2·5 × 10?4 M . It seems that the interfacial adsorption of pyridine carboxylates and of 4-octylphenylamine is not the decisive phenomenon in palladium(II) extraction. The negligible protonation of the pyridine-type extractants and the phase transfer catalysis explains well the quick extraction of palladium(II) with the commercial and highly hydrophobic extractant ACORGA CLX-50. 相似文献
68.
Oscar A. Garro Emilio Rodríguez Roberto Palacios Unda Danley A. S. Callieri 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》1995,63(4):367-373
The kinetics of alcoholic fermentation of a strain of Zymomonas mobilis, isolated from sugarcane juice, has been studied with the objective of determining the constansts of a non-structured mathematical model that represents the fermentation process. Assays in batch and in continuous culture have been carried out with different initial concentrations of glucose. The final concentrations of glucose, ethanol and biomass were determined. The following kinetic parameters were obtained: μmax, 0·5 h?1; Ks, 4·64 g dm?3; Pmax, 106 g dm?3; Yx/s, 0·0265 g g?1; m, 1·4 g g?1 h?1; α, 17·38 g g?1; β, 0·69 g g?1 h?1. 相似文献
69.
Chestnuts were dehydrated by using a combined method of osmotic dehydration followed by air drying. Samples were osmotically pretreated with sucrose (60% w/w) and glucose (56% w/w) for 8 h, air-dried at temperatures of 45, 55, and 65°C, at a relative humidity of 30% and at a velocity of 2.7 m·s-1 and the experimental data of the drying kinetics were obtained. Whole samples were dried with different peelings: (a) removal of endocarp and pericarp (peeled) and (b) additionally the internal rough surface (cut). In all cases, cut chestnuts show greater drying rates than peeled samples, indicating that a significant mass transfer resistance in the layer nearest to the surface takes place. Peeled samples pretreated with sucrose solutions behave in a similar way to untreated samples. For the rest of the samples, the cut samples osmotically treated with sucrose solutions and all the samples treated with the glucose solution, the drying rates decrease during drying. Drying kinetics are successfully modeled by employing a diffusional model that takes the shrinkage into account. The effective coefficient of water diffusion was evaluated and correlated with temperature. The quality of the final product was monitored by color change. In spite of the fact that the total color difference is not modified by the osmotic treatment, the L*, a*, and b* color coordinates of cut samples treated with sucrose and glucose solutions do undergo changes; the L* and a* coordinates change less than the b*. 相似文献
70.
本文测算了自蔓延高温合成TiAl基合金粉末的爆炸烧结特性常数值:γ=1.44,lgβ=25.25,并为试验证实,这为获取大尺寸TiAl基合金提供了理论依据。 相似文献