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应力波因子技术中一些问题的回顾和展望 总被引:7,自引:0,他引:7
首先就正在发展中的应力波因子技术的起源和思想进行了回顾,然后就该技术的早期工作进行了系统的归纳和评价,最后就该技术应用和理论研究的现状进行了评论并指出了将来应解决的问题。 相似文献
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电子机械系统微型化就是把不同功能的各种元器件封装到紧密空间, 目的在于分析有关封装设计负载下降的方案. 采用计算机程序配置发生器生成系统的热传递路径的几何构造和平面基板上热分布作为样本的方法,把这些构造的温度解决方案压缩进入快速估计公式中,使封装设计能够自由地进行相关的热传递分析. 通过涉及到几何学方面复杂的传热路径的系统热传递分析,快速完成每个设计改变. 结果表明系统微型化热设计,就是系统构造和整个向周围环境热损耗之间的耦合,就是热通过自然对流和辐射,从系统外壳上的一个区域向周围扩散. 最后得出结论,外壳材料热传导性跨越的参数领域,以及系统的性能长度为系统级热传递领域,对系统的构造敏感.性能长度对塑料封装系统而言约为1cm,对陶瓷及合金封装约为3~10cm,在铜或铝金属包层系统为10~40 cm. 相似文献
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Poly(propylene carbonate) (PPC) was synthesized by the zinc glutarate catalyzed copolymerization of carbon dioxide and propylene oxide (PO). Hydrolytic degradability of the PPC polymer was examined in tetrahydrofuran solutions containing 10 wt.% acidic or basic aqueous solutions of varying pH using viscometry and GPC analysis. Further, the hydrolysis behaviors of all PPC solutions were compared with those of poly(com/scidirimg/entities/25b.gif" alt="var epsilon" title="var epsilon" border="0">-caprolactone) (PCL) and poly(d,l-lactic acid) (PLA). All polymers studied show higher degradability in strong basic conditions than in strong acidic conditions, but very low degradability in moderate acidic, basic and neutral conditions. Moreover, PPC is degraded less in strong acidic conditions than the polyesters, while in strong basic conditions, the polycarbonate is more easily degraded. The difference in degradabilities of these polymers in acidic conditions is associated with the different nucleophilicities of their carbonyl oxygen atoms, while in basic conditions the differences are associated with the different electrophilicities of the corresponding carbonyl carbon atoms. With regard to the hydrolysis results and the structural and chemical nature of the polymer backbones, degradation mechanisms are proposed for the acid- and base-catalyzed hydrolyses of PPC, PCL and PLA. 相似文献
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Jos E. Bez ngel Marcos-Fernndez Rosa Lebrn-Aguilar Antonio Martínez-Richa 《Polymer》2006,47(26):8420-8429
A new convenient route for the synthesis of poly(com/scidirimg/entities/25b.gif" alt="var epsilon" title="var epsilon" border="0">-caprolactone) (PCL) with α,ω-telechelic diols' end-groups is presented. Synthesis of α,ω-telechelic PCL diols (HOPCLOH) was achieved by ring-opening polymerization (ROP) of com/scidirimg/entities/25b.gif" alt="var epsilon" title="var epsilon" border="0">-caprolactone (CL) catalyzed with ammonium decamolybdate (NH4)8[Mo10O34] and using diethylene glycol (DEG) as initiator. Obtained HOPCLOH was characterized by 1H and 13C NMR, FT-IR, GPC and MALDI-TOF. Comparative studies demonstrate that ammonium decamolybdate (NH4)8[Mo10O34] is better catalyst than Sn-octanoate (SnOct2) toward CL polymerization in presence of DEG, under the conditions tested. A biodegradable poly(ester-urethane-urea) derivative was efficiently prepared from synthesized HOPCLOH. Obtained polymer shows minor differences with respect to the properties recorded for a poly(ester-urethane-urea) obtained from commercial HOPCLOH. 相似文献
67.
Tatiana V. Magdesieva Magdalena Graczyk Oleg M. Nikitin Kim P. Butin 《Electrochimica acta》2006,52(3):1265-1280
We have studied a reaction between the reduced form of titanocene dichloride (Cp2TiCl2) and a group of organic halides: benzyl derivatives (4-Xcom/sd/entities/sbnd" class="glyphImg">C6H4CH2Cl, X = H, NO2, CH3; 4-Xcom/sd/entities/sbnd" class="glyphImg">C6H4CH2Br, X = H, NO2, PhC(O); 4-Xcom/sd/entities/sbnd" class="glyphImg">C6H4CH2SCN, X = H, NO2) as well as three aryl halides (4-NO2C6H4Hal, Hal = Cl, Br; 4-CH3O-C6H4Cl). It has been shown that the electrochemical reduction of Cp2TiCl2 in the presence of these benzyl halides leads to a catalytic cycle resulting in the reductive dehalogenation of these organic substrates to yield mostly corresponding toluene derivatives as the main product. No dehalogenation has been observed for aryl derivatives. Based on electrochemical data and digital simulation, possible schemes of the catalytic process have been outlined. For non-substituted benzyl halides halogen atom abstraction is a key step. For the reaction of nitrobenzyl halides the complexation of Ti(III) species with the nitro group takes place, with the electron transfer from Ti(III) to this group (owing to its highest coefficient in LUMO of the nitro benzyl halide) followed by an intramolecular dissociative electron redistribution in the course of the heterolytic Ccom/sd/entities/sbnd" class="glyphImg">Hal bond cleavage.The results for reduced titanocene dichloride centers immobilized inside a polymer film showed that the catalytic reductive dehalogenation of the p-nitrobenzyl chloride does occur but with a low efficiency because of the partial deactivation of the film due to the blocking of the electron charge transport between the electrode and catalytic centers. 相似文献
68.
The requirement for higher quality drinking water necessitates the application of more efficient water treatment techniques. Nanofiltration is one promising option for enhanced water treatment, for example, in enhanced organic matter removal. The characteristics of different nanofiltration membranes vary remarkably, and the selection of a membrane has to be made according to the requirements of an application. In this study six nanofiltration membranes (NF70, NF255, NTR-7450, NTR-7410, Desal-5 and TFC-S) were evaluated in improving the quality of chemically pre-treated surface water in a pilot-scale process. The results indicate that the membrane with high organics removal and slightly reduced ion removal characteristics (NF255) performed best in terms of product water quality as well as membrane productivity and fouling. The most permeable membrane (NTR-7410) suffered intensive fouling and insufficient product water quality. An interesting finding was that the permeates of all the tested membranes possessed a significant potential for microbial growth, despite the low nutrient contents. 相似文献
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