全文获取类型
收费全文 | 57910篇 |
免费 | 8187篇 |
国内免费 | 4091篇 |
专业分类
电工技术 | 20496篇 |
综合类 | 4915篇 |
化学工业 | 3922篇 |
金属工艺 | 1109篇 |
机械仪表 | 2877篇 |
建筑科学 | 4316篇 |
矿业工程 | 4855篇 |
能源动力 | 1919篇 |
轻工业 | 1554篇 |
水利工程 | 1118篇 |
石油天然气 | 1052篇 |
武器工业 | 661篇 |
无线电 | 7181篇 |
一般工业技术 | 3154篇 |
冶金工业 | 1539篇 |
原子能技术 | 424篇 |
自动化技术 | 9096篇 |
出版年
2024年 | 262篇 |
2023年 | 839篇 |
2022年 | 1545篇 |
2021年 | 2008篇 |
2020年 | 2206篇 |
2019年 | 1676篇 |
2018年 | 1627篇 |
2017年 | 2164篇 |
2016年 | 2374篇 |
2015年 | 2782篇 |
2014年 | 4191篇 |
2013年 | 3523篇 |
2012年 | 4959篇 |
2011年 | 5226篇 |
2010年 | 3928篇 |
2009年 | 3926篇 |
2008年 | 3887篇 |
2007年 | 4425篇 |
2006年 | 3756篇 |
2005年 | 2924篇 |
2004年 | 2303篇 |
2003年 | 2018篇 |
2002年 | 1564篇 |
2001年 | 1350篇 |
2000年 | 1062篇 |
1999年 | 777篇 |
1998年 | 565篇 |
1997年 | 460篇 |
1996年 | 411篇 |
1995年 | 293篇 |
1994年 | 299篇 |
1993年 | 211篇 |
1992年 | 157篇 |
1991年 | 101篇 |
1990年 | 91篇 |
1989年 | 67篇 |
1988年 | 44篇 |
1987年 | 34篇 |
1986年 | 22篇 |
1985年 | 28篇 |
1984年 | 25篇 |
1983年 | 20篇 |
1982年 | 14篇 |
1981年 | 4篇 |
1980年 | 5篇 |
1979年 | 6篇 |
1974年 | 3篇 |
1970年 | 3篇 |
1959年 | 3篇 |
1951年 | 3篇 |
排序方式: 共有10000条查询结果,搜索用时 593 毫秒
51.
一种零电压转换有源功率因数校正电路的研究 总被引:1,自引:0,他引:1
提出了一种基于UC3854的零电压转换有源功率因数校正(ZVT-APFC)的控制电路实现方案,介绍了ZVT电路工作原理,着重分析了由分立元件构成的辅助开关管的驱动电路,通过实验证实了驱动电路的稳定性和可靠性,并通过效率比较验证了ZVT-APFC电路的优良性能。与采用UC3855的电路相比,该电路方案具有简单、可靠、成本低等优点。 相似文献
52.
采用凝胶成型法制备加氢催化剂载体,并进行了工业放大试验。通过BET、NH3-TPD、H2-TPR等表征手段及实际的加氢反应性能评价对凝胶成型法制备的载体及加氢催化剂与常规方法进行对比分析,结果表明,采用凝胶成型法所制得的载体及催化剂均具有较高的孔体积和比表面积、较低的堆密度,其机械强度可满足工业要求,总酸量及中强酸酸量得到提升,催化剂活性组分与载体强结合力得到削弱,金属利用率提高,应用性能明显优于传统方法制备的加氢催化剂载体。通过该方法完成了加氢催化剂载体的工业生产,所生产的载体应用于天津院THDS-3加氢精制催化剂取得了良好的工业应用效果。 相似文献
53.
J. Gegner 《Materialwissenschaft und Werkstofftechnik》2003,34(3):290-297
Chemical Composition and Microstructure of Polymer‐Derived Glasses and Ceramics in the Si–C–O System. Part 2: Characterization of microstructure formation by means of high‐resolution transmission electron microscopy and selected area diffraction Liquid or solid silicone resins represent the economically most interesting class of organic precursors for the pyrolytic production of glass and ceramics materials on silicon basis. As dense, dimensionally stable components can be cost‐effectively achieved by admixing reactive filler powders, chemical composition and microstructure development of the polymer‐derived residues must be exactly known during thermal decomposition. Thus, in the present work, glasses and ceramics produced by pyrolysis of the model precursor polymethylsiloxane at temperatures from 525 to 1550 °C are investigated. In part 1, by means of analytical electron microscopy, the bonding state of silicon was determined on a nanometre scale and the phase separation of the metastable Si–C–O matrix into SiO2, C and SiC was proved. The in‐situ crystallization could be considerably accelerated by adding fine‐grained powder of inert fillers, such as Al2O3 or SiC, which permits effective process control. In part 2, the microstructure is characterized by high‐resolution transmission electron microscopy and selected area diffraction. Turbostratic carbon and cubic β‐SiC precipitate as crystallization products. Theses phases are embedded in an amorphous matrix. Inert fillers reduce the crystallization temperature by several hundred °C. In this case, the polymer‐derived Si–C–O material acts as a binding agent between the powder particles. Reaction layer formation does not occur. On the investigated pyrolysis conditions, no crystallization of SiO2 was observed. 相似文献
54.
We report on picosecond time resolved spectroscopy of photogenerated infrared active vibrations in thin films of 2,5-dioctyloxy poly(phenylene vinylene). We excited the films by ?4 ps long pulses of 565 nm laser light with 2×1013 photons/cm2 per pulse and repetition rate of 76 MHz. We then followed the temporal evolution of the infrared active vibrational (IRAV) spectrum using a subsequent, variably delayed, weak tunable IR probe pulses of similar temporal duration. Under these conditions, we show clear spectroscopic evidence for photogenerated infrared active vibrations at times which are shorter than our temporal resolution (<4 ps). We suggest that the transient IRAV absorption is due to secondary polarons formation following exciton dissociation. 相似文献
55.
基于Intranet/Internet的大坝安全监测信息查询系统 总被引:2,自引:2,他引:0
大坝安全监测信息的网上发布可以让人们了解各种实时、动态信息,文 中主要介绍了在Intranet/Internet下采用ASP(active server pages)结合VBScript,JavaS cript及ActiveX技术进行大坝安全监测信息查询系统开发的方法及步骤,并结合实际系统的 开发加以说明。 相似文献
56.
本文介绍了欧洲轿车新战略决策,也即:将要提高轿车的电池电压,,阻燃材料的比率和工作温度;Synolite5001-T-1牌聚酯树脂的阻燃防炎性能优于酚醛树脂。 相似文献
57.
NMOS器件两次沟道注入杂质分布和阈电压计算 总被引:1,自引:1,他引:0
分别考虑了深浅两次沟道区注入杂质在氧化扩散过程中对表面浓度的贡献。对两次注入杂质的扩散分别提取了扩散系数的氧化增强系数、氧化衰减系数和有效杂地系数,给出了表面浓度与工艺参数之间的模拟关系式,以峰值浓度为强反型条件计算了开启电压,文章还给出了开启电压、氧化条件、不同注入组合之间的关系式。 相似文献
58.
一种基于阵列式触觉传感器的主动触觉搜索方法及仿真 总被引:2,自引:1,他引:1
本文在一种二指节手指模型的基础上,提出了一种新的主动触觉搜索策略和方法,综合利用阵列式触觉传感铭的输出图象来不断改变机械手的姿态,从而依次有序地搜索到三维物体的特征点,并据此生成物体的三维图形。此外还讨论了上述方法的计算机仿真实现。 相似文献
59.
Nitric oxide reduction and carbon monoxide oxidation over carbon-supported copper-chromium catalysts 总被引:1,自引:0,他引:1
S. Stegenga R. van Soest F. Kapteijn J. A. Moulijn 《Applied catalysis. B, Environmental》1993,2(4):257-275
Carbon supported copper-chromium catalysts are shown to be very active for both the reduction of nitric oxide with carbon monoxide and the oxidation of carbon monoxide with oxygen. Mixed copper-chromium oxide active phases have good activity in the simultaneous removal of nitric oxide and carbon monoxide from exhaust gases. The influence of several catalyst variables has been investigated. The activity per volume of catalyst increases with increasing loading, while the intrinsic activity shows a maximum around C/M=100−50. An optimum catalyst for nitric oxide reduction and carbon monoxide oxidation has a copper/chromium ratio of 2/1. The apparent activation energy for the carbon monoxide oxidation over carbon supported copper-chromium catalysts is 77 kJ/mol, suggesting that the Cu---O bond rupture is the rate-limiting process. The reduction of nitric oxide takes place at higher temperatures. Since all catalysts have a low selectivity for molecular nitrogen formation at lower temperatures, the dissociation of nitric oxide is probably rate determining, resulting in a slightly reduced catalyst system. In an excess of carbon monoxide the reaction is first-order in nitric oxide and zero-order in carbon monoxide. Moisture inhibits the reaction by reversible competitive adsorption, whereas carbon dioxide does not. Oxygen completely inhibits the reduction of nitric oxide due to the more rapid reoxidation of the catalytic sites compared to nitric oxide. Therefore, the reduction of nitric oxide takes place only when all oxygen has been converted and, hence, is shifted to higher temperatures. As a possible consequence, the production of nitrous oxide is reduced. Nitric oxide and molecular oxygen react preferentially with carbon monoxide, so, in an excess of oxidizing component, gasification of the carbon support occurs at higher temperatures after carbon monoxide has been completely consumed. 相似文献
60.