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M.C. García-Gutiérrez A. Nogales C. Domingo G. Broza K. Schulte T.A. Ezquerra 《Polymer》2006,47(1):341-345
We report the appearance of a novel self-assembling of a fraction of single-wall carbon nanotubes (SWCNT) within a SWCNT-polymer nanocomposite subjected to flow fields upon injection molding processing. By combining X-ray diffraction and Raman spectroscopy techniques, both working on a microfocus fashion, we probe that a fraction of the thinnest SWCNT self-assembles into a rectangular lattice in the sample regions where the shear stress induces the highest levels of nanotube aggregation. Additionally, we demonstrate that a modest amount in weight of nanotubes is enough to template the morphology of crystallization during flow providing a method to obtain a highly desirable fiber-like morphology. 相似文献
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通过在结晶器保护渣中添加Li2O和B2O3作助熔剂,在实验室内模拟渣膜的形成条件,结合岩相和扫描电镜能谱分析,研究了Li2O3和B2O3对含稀土氧化物保护渣结晶矿物组成的影响.结果表明:稀土氧化物可以促进保护渣中枪晶石析出,抑制玻璃相形成,提高保护渣结晶率;当稀土氧化物含量达到一定数值,保护渣结晶矿物中可以形成稀土硅酸钙相,稀土氧化物继续增加,会有未溶稀土氧化物固态质点出现;保护渣中加入少量B2O3和Li2O作助熔剂,不仅可以促进硅灰石生成,而且能够有效抑制高熔点的枪晶石和稀土硅酸钙形成,防止渣膜形成过程中过早析出高熔点相. 相似文献
115.
Oleic acid (OA)-modified CaCO3 nanoparticles were prepared using surface modification method. Infrared spectroscopy (IR) was used to investigate the structure of the modified CaCO3 nanoparticles, and the result showed that OA attached to the surface of CaCO3 nanoparticles with the ionic bond. Effect of OA concentration on the dispersion stability of CaCO3 in heptane was also studied, and the result indicated that modified CaCO3 nanoparticles dispersed in heptane more stably than unmodified ones. The optimal proportion of OA to CaCO3 was established. The effect of modified CaCO3 nanoparticles on crystallization behavior of polypropylene (PP) was studied by means of DSC. It was found that CaCO3 significantly increased the crystallization temperature, crystal-lization degree and crystallization rate of PP, and the addition of modified CaCO3 nanoparticles can lead to the for-mation of β-crystal PP. Effect of the modified CaCO3 content on mechanical properties of PP/CaCO3 nanocompo-sites was also studied. The results showed that the modified CaCO3 can effectively improve the mechanical proper-ties of PP. In comparison with PP, the impact strength of PP/CaCO3 nanocomposites increased by about 65% and the flexural strength increased by about 20%. 相似文献
116.
The crystallization behavior of polypropylene (PP) copolymer obtained by in situ reactor copolymerization with or without a nucleating agent and/or nano‐CaCO3 particles was investigated both by thermal analysis and by polarized light microscopy. The Avrami model is successfully used to describe the crystallization kinetics of the studied copolymer. The results of the investigation show that a dramatic decrease of the half‐time of crystallization t1/2, as well as a significant increase of the overall crystallization rate, are observed in the presence of the nucleating agent. These effects are further promoted in the presence of the nano‐CaCO3 particles. The incorporation of the nucleating agent and nano‐CaCO3 particles into PP copolymer remarkably improved the mechanical properties and heat distortion temperature. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 431–438, 2004 相似文献
117.
在TS-2分子筛胶液制备过程中,添加了络合稳定剂H2O2。实验分析表明:钛酸四丁酯与H2O2形成过氧化钛物种,可以有效避免锐钛矿TiO2形成,提高骨架钛含量,在高温条件下晶化仍能得到催化性能较好的TS-2分子筛。利用丙烯环氧化反应对TS-2分子筛进行了考评,H2O2的转化率可达94%,H2O2生成PO的选择性可达97%。反应体系的酸碱性对环氧化产物分布影响显著,碱性物质的加入可以显著提高PO的选择性,抑制PO和溶剂发生的副反应,但是过量的碱性添加物会造成TS-2分子筛的失活。 相似文献
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Polypropylene (PP) was blended with a linear low-density polyethylene (LLDPE, containing 5% hexene comonomer) over a composition range of 10–90% of PP. The crystallization and morphology of the PP–LLDPE blends were studied by differential scanning calorimetry (DSC), polarized optical microscopy with a hot stage (HSOM), and scanning electron microscopy (SEM). In particular, the isothermal crystallization of PP in molten LLDPE was investigated. It was observed that the crystallization and melting behavior of PP and LLDPE changed in the blends, indicating that there was some degree of miscibility between the PP and the LLDPE. A depression of the equilibrium melting temperature (T) of PP in the blends with no more than 15% of PP confirmed that PP was miscible with LLDPE at and below 15% of PP. In addition, a drastic decrease in T from the 25% PP blend to the 20% blend led us to conclude that the miscible behavior between PP and LLDPE became favorable at a PP concentration of 20%. The optical microscopic images showed that, in the blends with 10 and 15% of PP, the PP crystallized as open-armed diffuse spherulites, similar to those in the miscible blends. In contrast, the PP crystallized in a phase-separated matrix or droplets with more than 25% of PP, when obvious phase separation occurred. The SEM image revealed that the PP lamella was able to penetrate the PP and LLDPE phase boundary and grow in the LLDPE phase. The above results displayed that the PP dissolved in the LLDPE, and, particularly, when the PP concentration was below 20%, the dissolution was substantial. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 82: 628–639, 2001 相似文献