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This paper describes a new reactive blending approach to improve the compatibility of poly(l-lactide) (PLLA) and poly(?-caprolacton) (PCL). For this purpose, the ring-opening polymerization of l-lactide (LLA) was carried out in the presence of PCL-OH (OH groups on one end). The P(CL-b-LLA) block copolymers were in situ formed during polymerization, and as a result, PLLA/P(CL-b-LLA) blends were obtained. The characterization of GPC and 1H NMR verified the synthesis of PLLA/P(CL-b-LLA) blends. Furthermore, the 13C NMR spectroscopy showed that no transesterification reaction occurred to a significant extent during LLA polymerization process. The in situ formed P(CL-b-LLA) compatibilizes the phase separated structure of PCL domains in PLLA matrix. The size of PCL domains in PLLA matrix became much smaller than that in a solution blended sample. The average sizes of PCL domains are controllable in the level of sub-micron scale. 相似文献
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The melting behavior and nonisothermal crystallization kinetics of pure polyamide 6 (PA 6) and its molecular composites with polyamide 66 (PA 66) were investigated with differential scanning calorimetry. The PA 6/PA 66 composites had one melting peak, whereas the coextruded PA 6/PA 66 blends had two melting peaks. With the addition of PA 66 to PA 6 via in situ anionic polymerization, the melting temperature, crystallization temperature, and crystallinity of PA 6 in the composites decreased. The half‐time of nonisothermal crystallization increased for a PA 6/PA 66 molecular composite containing 12 wt % PA 66, in comparison with that of pure PA 6. The commonly used Ozawa equation was used to fit the nonisothermal crystallization of pure PA 6 and its composites. The Ozawa exponent values in the primary stage were equal to 1.28–3.03 and 1.28–2.97 for PA 6 and its composite with 12 wt % PA 66, respectively, and this revealed that the mechanism of primary crystallization of PA 6 and PA 6/PA 66 was mainly heterogeneous nucleation and growth. All the results indicated that the incorporation of PA 66 into PA 6 at the molecular level retarded the crystallization of PA 6. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 2172–2177, 2005 相似文献
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从可持续发展视角,研究了装备维修保障可持续发展基本问题,界定了装备维修保障可持续发展的内涵,描述了装备维修保障可持续发展的主要目标,分析了装备维修保障可持续发展的立足点和动力源,总结了装备维修保障可持续发展对价格机制创新的内在要求。 相似文献
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Parametric Stabilization of Quantized Interconnected Systems with Application to Coupled Inverted Pendulums 下载免费PDF全文
Ning Chen Guisheng Zhai Yuqian Guo Weihua Gui Xiaoyu Shen 《Asian journal of control》2015,17(3):1061-1069
This paper studies the analysis of parametric stability and decentralized state feedback control of a kind of quantized interconnected systems. The output of each controller is quantized logarithmically before it is input to the subsystem, and the quantized density would affect the stability of the systems. First, a decentralized state feedback controller is designed for interconnected systems without quantization and the corresponding stable region is obtained. Second, for a given controller, the lower bound of the quantization density is evaluated from parameters of local controllers. Finally, the proposed method is applied to coupled inverted pendulums systems which can be viewed as quantized interconnected systems. The simulation results show that by using the proposed quantized controllers, the interconnected inverted pendulum systems are parametrically stabilized. 相似文献
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Multi-Agent协商是目前研究的一个热点,而从底层开发出一个Multi-Agent协商系统是非常复杂和困难的。该文在研究JADE仿真平台技术的基础上,对基于JADE仿真平台的Multi-Agent协商进行了设计与实现,为研究Multi-Agent协商有着重要的意义。 相似文献
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Jiafeng Zhu Qingyuan Bi Yinghao Tao Wenyao Guo Jinchen Fan Yulin Min Guisheng Li 《Advanced functional materials》2023,33(15):2213131
Designing and developing visible-light-responsive materials for solar to chemical energy is an efficient and promising approach to green and sustainable carbon-neutral energy systems. Herein, a facile in situ growth hydrothermal strategy using Mo-modified ZnIn2S4 (Mo-ZIS) nanosheets coupled with NiTiO3 (NTO) microrods to synthesize multifunctional Mo-modified ZIS wrapped NTO microrods (Mo-ZIS@NTO) photocatalyst with enhanced interfacial electric field (IEF) effect and typical S-scheme heterojunction is reported. Mo-ZIS@NTO catalyst possesses wide-spectrum light absorption properties, excellent visible light-to-thermal energy effect, electron mobility, charges transfer, and strong IEF and exhibits excellent solar-to-chemical energy conversion for efficient visible-light-driven photocatalytic hydrogen evolution. Notably, the engineered Mo1.4-ZIS@NTO catalyst exhibits superior performance with H2 evolution rate of up to 14.06 mmol g−1 h− 1 and the apparent quantum efficiency of 44.1% at 420 nm. The scientific explorations provide an in-depth understanding of microstructure, S-scheme heterojunction, enhanced IEF, Mo-dopant facilitation effect. Moreover, the theoretical simulations verify the critical role of Mo element in promoting the adsorption and activation of H2O molecules, modulating the H adsorption behavior on active S sites, and thus accelerating the overall catalytic efficiency. The photocatalytic hydrogen evolution mechanism via S-scheme heterojunction with adjustable IEF regulation over Mo1.4-ZIS@NTO is also demonstrated. 相似文献