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主要研究了CDMA蜂窝通信系统的工作原理,且以基于IS-95标准的前向链路为主。利用MATLAB软件建立了前向链路中各器件的模块,实现了CDMA基带信号发生器,并在时域及频内进行了测量。 相似文献
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S—135钢板是水电站用高强耐磨不锈钢板,既要求强度高、韧性好,又要求耐磨、耐蚀性强,生产难度较大。除我厂外,目前国内尚无其它厂家能够生产这种钢板。该钢板在加热轧制,冷却过程中要解决很多技术难点。我们通过采用特殊的控制轧制和控制冷却工艺,很好地解决了诸多技术难点,使S—135钢板的开发研制取得了成功。为电站用高强度耐磨不锈钢生产提供了宝贵的经验,也为控制轧制及控制冷却技术在中板生产行业的应用起到了积极的推动作用。 相似文献
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Muhammad Khurram Tufail Niaz Ahmad Le Yang Lei Zhou Muhammad Adnan Naseer Renjie Chen Wen Yang 《中国化学工程学报》2021,39(11):16-36
The development of an inorganic electrochemical stable solid-state electrolyte is essentially responsible for future state-of-the-art all-solid-state lithium batteries (ASSLBs). Because of their advantages in safety, working temperature, high energy density, and packaging, ASSLBs can develop an ideal energy storage system for modern electric vehicles (EVs). A solid electrolyte (SE) model must have an economical synthesis approach, exhibit electrochemical and chemical stability, high ionic conductivity, and low interfacial resistance. Owing to its highest conductivity of 17 mS·cm-1, and deformability, the sulfide-based Li7P3S11 solid electrolyte is a promising contender for the high-performance bulk type of ASSLBs. Herein, we present a current glimpse of the progress of synthetic procedures, structural aspects, and ionic conductivity improvement strategies. Structural elucidation and mechanistic approaches have been extensively discussed by using various characterization techniques. The chemical stability of Li7P3S11 could be enhanced via oxide doping, and hard and soft acid/base (HSAB) concepts are also discussed. The issues to be undertaken for designing the ideal solid electrolytes, interfacial challenges, and high energy density have been discoursed. This review aims to provide a bird's eye view of the recent development of Li7P3S11-based solid-state electrolyte applications and explore the strategies for designing new solid electrolytes with a target-oriented approach to enhance the efficiency of high energy density all-solid-state lithium batteries. 相似文献
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The insecticidal nonprotein amino acid S-(-carboxyethyl)-cysteine (S-CEC) is the major free amino acid in the seeds of severalCalliandra spp. where it accounts for up to 2.9 % of dry weight. Lesser amounts of other related S-containing amino acids and an array of nonprotein imino acids derived from pipecolic acid are other constituents. High concentrations of imino acids, which also show insecticidal activity, are maintained in the mature leaves, but sulfur compounds are lacking. In this study the disappearance of S-CEC from the germinating seeds and young seedlings ofC. rubescens was monitored over time. After 10 weeks, S-CEC continues to be found in high concentrations in the stems and new leaves. As young leaves mature, sulfur compounds quickly decrease in concentration. Traces of S-CEC are found in new leaves of plants up to nine months after germination. Whether high concentration of S-CEC in young leaves is due to transportation from the seed or de novo synthesis is unclear. The ecological implications are discussed. 相似文献
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In this paper, we present an analysis and synthesis approach for guaranteeing that the phase of a single-input, single-output closed-loop transfer function is contained in the interval [−α,α] for a given α>0 at all frequencies. Specifically, we first derive a sufficient condition involving a frequency domain inequality for guaranteeing a given phase constraint. Next, we use the Kalman–Yakubovich–Popov theorem to derive an equivalent time domain condition. In the case where S-1-26/0?wchp=dGLbVlW-zSkzk" alt="View the MathML source" title="View the MathML source" align="absbottom" border="0" height=16 width="39"/>, we show that frequency and time domain sufficient conditions specialize to the positivity theorem. Furthermore, using linear matrix inequalities, we develop a controller synthesis approach for guaranteeing a phase constraint on the closed-loop transfer function. Finally, we extend this synthesis approach to address mixed gain and phase constraints on the closed-loop transfer function. 相似文献
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采用分步溶剂萃取法对脂肪酶Novozyme 435催化2,2-二甲基环丙烷甲酸乙酯(DMCPE)不对称水解得到的S-(+)-2,2-二甲基环丙烷甲酸(S-(+)-DMCPA)制备液进行萃取分离.结果表明,采用等体积正己烷为萃取剂,在35℃和200r/min下,对酶法制备液萃取3次,每次萃取40min,底物DMCPE的萃取收率可达99.2%;继而采用等体积的乙酸乙酯在30℃,200r/min条件下,对萃余液进行2次萃取,每次萃取30min,产物S-(+)-DMCPA的萃取收率为99.5%.该研究对从酶法制备液中实现产物S-(+)-DMCPA的分离和未转化底物DMCPE的回收再利用,以及今后该分离过程的放大具有一定的借鉴和指导意义. 相似文献
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