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71.
The swelling behavior and the elastic properties of nanocomposite hydrogels have been investigated. The hydrogels were prepared by free-radical polymerization of the monomers acrylamide (AAm), N,N-dimethylacrylamide (DMA), and N-isopropylacrylamide (NIPA) in aqueous clay suspensions at 21 °C. Laponite with a radius of gyration in distilled water of 20 nm was used as clay particles in the hydrogel preparation. The reactions with AAm monomer were carried out in the presence of the chemical crosslinker N,N′-methylenebis(acrylamide) (BAAm). It was found that the volume of nanocomposite hydrogels immersed in water rapidly increases and attains a maximum value after about one day. Surprisingly, further increase in the swelling time results in the deswelling of the gels until they reach a limiting swelling ratio after about 5 days. This unusual swelling behavior is observable only when the clay concentration in the hydrogel is above the overlap threshold c∗. Swelling measurements combined with the elasticity tests show that the effective crosslink density first decreases, but then increases with increasing time of swelling of the hydrogels. The results were explained in terms of the rearrangements of the highly entangled polymer chains and clay particles during the gel volume change. 相似文献
72.
抗静电可染丙纶的结构与性能 总被引:1,自引:0,他引:1
研究了聚丙烯、抗静电组分、可染组分三元共混体系纤维的抗静电性能、力学性能、染色性能及形态结构。研究表明:抗静电组分和可染组分有一定的相互影响,当抗静电组分加入量在4%~6%;而可染组分加入量在8%~10%时为共混体系的最佳配合范围,共混纤维成品丝既表现出良好的抗静电性能,又表现出良好的可染性能,实现了常压沸染深色的效果。还发现,共混纤维拉伸丝的比电阻小于卷绕丝的比电阻。 相似文献
73.
A copolymer of 4‐vinylpyridine (4‐VP) and styrene was synthesized by radical mass polymerization using 2,2′‐azobisisobutyronitrile as initiator. An insoluble (linear) pyridinium‐type polymer was prepared by the reaction of P (4VP–St) with 1‐bromooctane. An anion exchange membrane was prepared using a composite of pyridinium‐type polymer and a fibrous woven structure for use in electrochemistry. The composite membrane was characterized by X‐ray diffraction, tensile strength, scanning electron microscopy, and electrochemistry measurements. The experimental results showed that the fibrous woven product had improved the tensile strength more than had the membrane made of a pyridinium‐type polymer alone. The composite membrane was used in alkaline fuel cells, and its properties were measured by electrochemical analysis. The ionic conductivity of the membrane was acceptable, but its performance as a direct methanol fuel cell (DMFC) was not. The primary reason for this was analyzed, and research is ongoing, with analysis to be discussed in later reports. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 2248–2251, 2006 相似文献
74.
Copolymers of poly(acrylamide-co-acryloyloxyethyltrimethylammonium chloride or AM–CMA) and poly(acrylamide-co-methacryloyloxyethyltrimethylammonium chloride or AM–CMA) prepared by inverse emulsion polymerization were characterized by different analytical techniques. The chemical composition of the copolymers was estimated by elemental analysis and by nuclear magnetic resonance spectroscopy (NMR). NMR spectroscopy and computer simulation were further used for investigating the polymers' sequence distribution. The poly(AM–CMA) copolymers are chemically more homogeneous than are the poly(AM–CMA). The configurational propagation of dyads and triads for the homopolymers obeys Bernouilli's statistics. For the copolymers, the chemical sequences distribution is governed by Markov's first-order statistics. 相似文献
75.
NC74-1型氨合成催化剂的升温还原及应用 总被引:1,自引:0,他引:1
介绍了NC74-1氨合成催化剂在山东华鲁恒升化工股份有限公司大氮肥氨合成的装填、升温还原及使用情况。 相似文献
76.
庄日道 《网络安全技术与应用》2014,(8):71-71
随着网络的逐步普及,局域网的建设走向信息化已成为必然选择,它不仅为现代化教学,综合化信息管理,办公自动化等一系列应用提供基本操作平台而且能提供多种服务。本人联系工作实践,阐述局域网常见故障和处理的方法,并针对计算机局域网常见硬件故障,提出相应处理对策。 相似文献
77.
Some volatile acids were found to dramatically reduce the effectiveness of additives based on 2,2,6,6-tetramethylpiperidine as photostabilizers for polypropylene films. Strong acids such as HCl, HBr, and HNO3 had the largest effect with sulfurous acid somewhat less detrimental. Weak organic acids did not impair the effectiveness of the hindered amine light stabilizers. The role of acid concentration and contact time were explored for the HCl–piperidyl additive system. Secondary and tertiary amines were included in the study as well as oligomeric additives and an N-oxyl derivative. The latter is less basic than the free amines, and it was correspondingly less effected by acid exposures. The possibilities for acid exposure during the compounding, fabrication, and use of stabilized polyolefin articles is discussed as well as the effects of acids in terms of proposed stabilization mechanisms for the hindered amines. 相似文献
78.
79.
Hatice Kaplan Can A. Lale Doan Zakir M. O. Rzaev Ayegül Hasegeli Uner Ali Güner 《应用聚合物科学杂志》2006,100(5):3425-3432
The ternary copolymerization of maleic anhydride (MA), vinyl acetate (VA), and acrylic acid (AA) [P(MA‐co‐VA‐co‐AA)], which is considered to be an acceptor–donor–acceptor system, was carried out in 1,4‐dioxane with benzoyl peroxide as an initiator at 70°C under a nitrogen atmosphere. Constants of complex formation for the monomer systems in the study were determined by UV–visible (hydrogen‐bonding complex) and 1H‐NMR (charge transfer complex) methods, respectively. The results show that polymerization of the P(MA‐co‐VA‐co‐AA) system proceeds by an alternating terpolymerization mechanism. It is shown that the synthesized copolymers have typical polyelectrolyte behavior, ability for reversible hydrolysis–anhydrization reactions, and semicrystalline structures. In these cases, including radical polymerization, and formation of semicrystalline structures, the hydrogen‐bonding effect plays a significant role. The in vitro cytotoxicities of the synthesized terpolymer and alternating copolymer were evaluated using Raji cells (human Burkitt lymphoma cell line). The antitumor activities of prepared anion‐active copolymers were studied using methyl–thiazol–tetrazolium colorimetric assay and 50% of the cytotoxic dose of each copolymer and terpolymer were calculated. Hydrolyzed P(MA‐co‐VA‐co‐AA) and P(MA‐alt‐AA) copolymers have sufficiently high antitumor activity, which depends on the amount of hydrogen‐bonding carboxylic groups and their regular distribution in the side chain of functional macromolecules. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 3425–3432, 2006 相似文献
80.
生物质与煤共燃研究(Ⅰ)生物质的低温热解 总被引:6,自引:4,他引:6
介绍了生物质与煤共燃的研究流程及其主要的研究方法,通过对三种主要农业剩余生物质(锯屑,谷壳和花生壳)热解过程中的失重率变化,物理性质变化,工业分析变化,元素分析变化和发热量变化的研究发现,三种生物质在热解温度220℃-300℃,热解时间30min-60min下进行低温热解时,热解过程主要受热解温度控制,受热解时间控制较弱,随热解温度升高,热解时间延长,生物质的热失重率逐渐升高,生物质逐渐变得易于研磨。在工业分析上挥发分逐渐减少,固定碳及灰分不断提高,水分含量大幅下降;在元素分析上O元素的含量不断下降,C元素的含量不断上升,从而发热量不断增加,研究表明,当热解温度为270℃-300℃时,热解生物质的各项性质可与煤接近。 相似文献