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101.
ABSTRACT: The absorbance of 2,2-diphenyl-1-picrylhydrazyl (DPPH) at 517 nm in methanol and acetone decreased by 20 and 35% for 120 min at 25 °C under light, respectively; in the dark it did not change significantly for 150 min. Decomposition of DPPH under 21% oxygen after 90 min under light was significantly higher than that under 1% oxygen. Absorbance of DPPH in pH 4 buffer solution in methanol, and in pH 10 buffer solution in acetone, decreased by 55 and 80%, respectively, under light for 120 min. The evaluation of antioxidant activity by the changes of DPPH absorbance should be carefully interpreted since the absorbance of DPPH at 517 nm is decreased by light, oxygen, pH, and type of solvent in addition to the antioxidant. 相似文献
102.
K. Y. Cheah T. S. Tang Fujio Mizukami Shu-ichi Niwa Makoto Toba Y. M. Choo 《Journal of the American Oil Chemists' Society》1992,69(5):410-416
A new catalyst, ruthenium-tin-alumina is found to selectively hydrogenate oleic acid to 9-octadecen-1-ol (oleyl + elaidyl
alcohol) at low pressure with high yield. Catalyst preparation methods, catalyst raw materials and activation conditions have
a significant effect on the activity of the catalyst. The optimum atomic ratio of ruthenium to tin is about 1:2. Catalyst
prepared by an improved sol-gel method shows higher activity and selectivity than catalysts prepared by impregnation and coprecipitation
methods. Chloride is found to have a negative effect on catalytic activity. The best catalyst is prepared from chloride-free
ruthenium and tin raw materials. Under the optimum reaction conditions of 250°C and 5.6 MPa, the selectivities for 9-octadecen-1-ol
and total alcohol (9-octadecen-1-ol + stearyl alcohol) formation are 80.9% and 97%, respectively, at a conversion of 81.3%. 相似文献
103.
乙基叔丁基醚/β分子筛膜反应精馏 总被引:2,自引:2,他引:0
研究了混合碳四和乙醇合成乙基叔丁基醚(ETBE)的反应精馏过程。实验以支撑β分子筛膜为催化精馏元件,异丁烯转化率高达95%,回流比和醇烯摩尔比是影响异丁烯转化率的主要因素。与甲基叔丁基醚(MTBE)的反应精馏过程相比,以乙醇取代甲醇,只需对MTBE生产的操作条件作一些简单的调整,就可在其生产装置上合成ETBE。 相似文献
104.
尼龙6/马来酸酐-苯乙烯多单体接枝聚丙烯反应共混物 总被引:8,自引:0,他引:8
用双螺杆挤出机制备了聚丙烯(PP)与尼龙6(PA6)的共混物.先用多组分熔融接枝的方法将马来酸杆(MAH)和苯乙烯(St)共同接枝于聚丙烯(PP)上,制得多单体接枝聚丙烯PP-g-(MAH-St),该接枝物具有较高的MAH接枝率。利用MFR、SEM、TEM和力学性能测试等分析方法,研究了多组分熔融接枝聚丙烯PP-g-(MAH-St)对PA6/PP共混物的形态结构和力学性能等的影响。结果表明,PP-g-(MAH-St)中的酸酐基团与PA6末端的氨基发生化学反应,原位形成的PP-PA6共聚物能有效地改善PA6与PP的相容性,可以使PP均匀地分散在PA6基体中,相区尺寸明显减小,可至0.1μm,并使共混物的力学性能得到均衡的提高,冲击韧性的提高尤其显著,达到了橡胶改性所难以达到的效果。 相似文献
105.
光催化氧化后四环素的分解率与COD去除率之间关系的探讨 总被引:1,自引:0,他引:1
以粉状无机半导体(ZnO)为催化剂,探讨了水溶液中四环素经光催化氧化分解率和COD去除率之间的关系。实验表明,在本实验中四环素的分解率和COD去除率之间有较好的正相关性。当反庆系统中有足量的活性催化剂和足够的光照时间时,绝大部分四环素将被较彻底地氧化分解成CO2,这不仅有助于光催化反应机理的研究,助于今后在环保中的实际应用。 相似文献
106.
107.
The bulk modification of SBS rubber with maleic anhydride in a mixing chamber of a Haake rheomixer was studied. The effect of temperature, maleic anhydride, and benzoyl peroxide concentrations on the grafting efficiency was evaluated. High grafting efficiency was achieved when the ratio of peroxide and maleic anhydride concentration was high. On the other hand, on this condition high insoluble fraction was generated. The addition of a diamine, 4,4′‐diaminediphenylmethane to the reaction mixture minimizes the amount of insoluble polymer. However, the grafted MAH content also decreases. The graft copolymer was characterized by infrared spectroscopy and the grafting extension was determined by titration. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2953–2960, 2002; DOI 10.1002/app.10355 相似文献
108.
Fusae Nakanishi 《Polymer International》1992,27(3):237-241
Preparation of photoreactive Langmuir-Blodgett (LB) films was carried out using polymers/oligomers prepared from long-chain dialkyl esters of di-and tetra-olefins and having cyclobutane rings in the main chain. These polymers/oligomers formed stable monolayers on a water surface when mixed with arachidic acid. These monolayers could be deposited onto a substrate successfully forming Y-type films. The oligomer LB films were polymerized on irradiation. The polymer LB films showed a photo-reversible process between polymers and oligomers, depending on wavelength of the irradiating light. On the basis of spectral data and molecular weight change, this behaviour was found to be caused by cleavage and formation of cyclobutane rings. 相似文献
109.
针对双组分等温平行反应体系,分析讨论了以提高催化剂活性和选择性为目标时催化剂活性组分的最优分布形式(为δ-函数分布),并给出了确定这种反应体系的催化剂的最佳活性层位置的计算方法。结果表明:以提高选择性为目标的最佳活性层位置比以提高活性为目标的要更靠近催化剂核心,实用的最优位置应介于二者之间。最后,本文还研究了反应动力学级数、本性选择性以及内扩散模数(Thiele 模数)等因素对最佳活性层位置的影响。 相似文献
110.
Marcus T. Schmitz Bashir M. Al-Hashimi Petru Eles 《Design Automation for Embedded Systems》2002,6(4):401-424
In this paper, we introduce the LOPOCOS (Low Power Co-synthesis) system, a prototype CAD tool for system level co-design. LOPOCOS targets the design of energy-efficient embedded systems implemented as heterogeneous distributed architectures. In particular, it is designed to solve the specific problems involved in architectures that include dynamic voltage scalable (DVS) processors. The aim of this paper is to demonstrate how LOPOCOS can support the system designer in identifying energy-efficient hardware/software implementations for the desired embedded systems. Hence, highlighting the necessary optimization steps during design space exploration for DVS enable architectures. The optimization steps carried out in LOPOCOS involve component allocation and task/communication mapping as well as scheduling and dynamic voltage scaling. LOPOCOS has the following key features, which contribute to this energy efficiency. During the voltage scaling valuable power profile information of task execution is taken into account, hence, the accuracy of the energy estimation is improved. A combined optimization for scheduling and communication mapping based on genetic algorithm, optimizes simultaneously execution order and communication mapping towards the utilization of the DVS processors and timing behaviour. Furthermore, a separation of task and communication mapping allows a more effective implementation of both task and communication mapping optimizationsteps. Extensive experiments are conducted to demonstrate the efficiency of LOPOCOS. We report up to 38% higher energy reductions compared to previous co-synthesis techniques for DVS systems. The investigations include a real-life example of an optical flow detection algorithm. 相似文献