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1.
Y. Cohen K. Landskron N. Ttreault S. Fournier‐Bidoz B. Hatton G.A. Ozin 《Advanced functional materials》2005,15(4):593-602
The synthesis and characterization of a novel silicon–silica nanocomposite material are reported. A self‐assembly method allows the encapsulation of silicon nanoclusters within the channels of a periodic mesoporous silica thin film. The result is the formation of a silicon–silica nanocomposite film with bright, room‐temperature photoluminescence in the visible range, and a nanosecond luminescence lifetime. The properties of the nanocomposite material have been studied by several analytical techniques, which collectively show the existence within the channels of non‐diamondoid‐structure‐type silicon nanoclusters with various hydrogenated silicon sites. It is estimated that the silicon nanoclusters in the silica mesoporous films occupy up to 39 % of the accessible pore volume. The nanocomposite film shows improved resistance to air oxidation compared to crystalline silicon. The high loading and chemical stability to oxidation under ambient conditions are important advantages in terms of the development of silicon‐based light‐emitting diodes from this class of materials. 相似文献
2.
3.
《中国稀土学报(英文版)》2022,40(10):1509-1518
Gd2O3:Eu3+@CsPbBr3 quantum dots (QDs) mesoporous hollow nanocomposites with good luminescent properties and high stability were built. Among which, the hollow Gd2O3:Eu3+ spheres and CsPbBr3 QDs were prepared by urea homogeneous precipitation and hot-injection method, respectively. Finally, the Gd2O3:Eu3+@CsPbBr3 QDs shell–core compounds were constructed through mechanical stirring. The structure, morphology, stability and luminescent properties were studied by Fourier transform infrared spectroscopy (FT-IR), differential scanning calorimetry/thermogravity (DSC/TG), X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), photoluminescence excitation/photoluminescence (PLE/PL) and life decay tools. Compared to the original CsPbBr3 QDs, Gd2O3:Eu3+@CsPbBr3 QDs display better photostability, thermal stability and current stability. The resulting Gd2O3:Eu3+@CsPbBr3 QDs composite exhibits good yellow emission. The Gd2O3:Eu3+@CsPbBr3 QDs mixed silicone resin was directly coated on the blue LED chip, then the w-LED device with the color coordinate of (0.31, 0.32) was successfully assembled. The Gd2O3:Eu3+@CsPbBr3 QDs compounds with excellent luminescent properties and stability are expected to be widely used in lighting and display areas. 相似文献
4.
MCM-41 silicates prepared in the presence of octyltrimethylammonium bromide either by a conventional method or by post-synthesis
hydrothermal treatment were characterized by nitrogen adsorption in a wide range of relative pressure from 10-6 to 1. Hydrothermally restructured samples were found to have lower BET surface areas, lower external surface areas and thicker
silica walls than the non-treated sample. More importantly, in addition to their characteristic mesopores (ca. 3 nm), they
were shown to have considerable amounts of micropores. The relative amount of micropores and mesopores was shown to be dependent
on the treatment conditions. Thus, it is demonstrated that the postsynthesis hydrothermal restructuring is a convenient synthesis
route to MCM-41 silicates with bimodal pore size distribution involving controllable amounts of microporosity.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
5.
S. Perathoner P. Lanzafame R. Passalacqua G. Centi R. Schlgl D.S. Su 《Microporous and mesoporous materials》2006,90(1-3):347-361
SBA15–TiO2 samples prepared by introducing titanium with a grafting method and having TiO2 loadings below 15 wt.% have been characterized by XRF, XRD, IR, porosimetry, SEM, HRTEM, and UV–Visible diffuse reflectance. Differently from the samples reported in the literature characterized by a high TiO2 loading, no evidences have been found for the presence of titania particles inside or outside the mesopores of SBA-15. Three different titanium species were instead evidenced to be present. The first two derive from the reaction of titanium with silanol groups in the corona area of inner SBA-15 walls leading to the formation of either TiO4 tetrahedral sites (by reaction by hydroxyl nests of surface defect sites) and/or pseudo-octahedral surface sites anchored by two (or more) Si or Ti ions through bridging oxygens. The third species derives from the reaction of titanium in the regions with high sylanol density, e.g. in the micropores located in the corona of SBA-15 channels, leading to the formation of TiO2-like nanoareas (probably Si-doped) with dimensions of around 1–2 nm maximum. The potential interest of these materials as photocatalysts, for the presence of a TiO2-like nanoareas highly accessible by reactants, is discussed. 相似文献
6.
Dehydrogenation of Light Alkanes Over Rhenium Catalysts on Conventional and Mesoporous MFI Supports 总被引:1,自引:0,他引:1
Anne Krogh Rovik Anke Hagen Iver Schmidt Søren Dahl Ib Chorkendorff Claus Hviid Christensen 《Catalysis Letters》2006,109(3-4):153-156
Recently, Re/HZSM-5 (Si/Al = 15) was shown to be an efficient catalyst for ethane dehydrogenation and aromatization at 823 K
and atmospheric pressure. In this reaction, the major initial products were benzene, toluene and xylene (BTX), but increasing
amounts of ethene were produced with time on stream due to deactivation of the catalyst. We show that by use of rhenium impregnated
MFI supports with very few or no acidic sites (Si/Al > 500), highly selective ethane dehydrogenation catalysts are obtained
with ethene selectivities of 98%. By use of mesoporous MFI supports (Si/Al >500) the lifetime of the catalyst appears to be
slightly improved compared to conventional MFI crystals. The beneficial effect of a mesoporous MFI support is convincingly
demonstrated in propane dehydrogenation, where both conversion and selectivities on the mesoporous MFI (Si/Al > 500) impregnated
with Re are significantly higher than on Re supported on a comparable conventional MFI support. 相似文献
7.
以酸性多孔ZSM-5沸石(HZSM-5-M)和高比表面积的氧化硅(SiO2)为载体,采用等体积浸渍法制备了负载Ni2P催化剂(Ni2P/HZSM-5-M和Ni2P/SiO2),对比研究了它们在苯乙炔选择性加氢反应中的催化性能。采用XRD、N2吸附-脱附、NH3-TPD、H2-TPR、SEM和TEM对载体及其负载的Ni2P催化剂进行了表征。催化剂活性结果为:当反应时间为2 h,苯乙炔在Ni2P/HZSM-5-M催化剂的转化率为98.5%,而在Ni2P/SiO2催化剂上仅为45.6%。说明Ni2P/HZSM-5-M催化剂的加氢活性显著高于Ni2P/SiO2催化剂。这是因为,与Ni2P/SiO2催化剂相比,在Ni2P/HZSM-5-M催化剂上形成了小颗粒的Ni2P活性相。同时,Ni2P/HZSM-5-M催化剂的活性具有良好的重复性。 相似文献
8.
9.
Nan Yao Guoxing Xiong Shishan Sheng Mingyuan He Weishen Yang Xinhe Bao 《Catalysis Letters》2002,78(1-4):37-41
A novel sol–gel process is used to synthesize mesoporous silica–alumina catalysts with controlled pore size distribution without using templates or pore-regulating agents. The nitrogen sorption analysis shows that the synthesized materials have high specific surface area in the range 587–692 m2/g and similar mesoporous distribution within 2–11 nm. Ultrasound is applied to prepare precursor silica–alumina sol with narrow particle diameter distribution. By calculation, it is found that ultrasonic treatment is able to provide 22.94 kJ/mol energy, which is just in accordance with the weak bond's bonding energy. Based on the calculation result, it is proposed that the role of ultrasonic treatment followed by acid peptization is to provide energy to break down the weak bonds. After gelation, the regular and close packing of similar-sized sol particles is capable of formation of controlled-sized interstices which are the precursors of mesopores. Solid-state 27Al MAS NMR and TEM are used to characterize the samples' structure and particle morphology. They show that most of the aluminum is located in the tetrahedral position in the present materials. According to TEM results, it is shown that the synthesized materials have spherical particles with size of about 15 nm. 相似文献
10.
Griselda A. Eimer Liliana B. Pierella Gustavo A. Monti Oscar A. Anunziata 《Catalysis Letters》2002,78(1-4):65-75
A novel route in the synthesis of Al-MCM-41 and Al-MCM-48, using tetraethoxysilane (TEOS) and sodium aluminate (NaAlO2) as Si and Al source has been obtained. The effect of surfactant nature and the synthesis conditions such as surfactant/Si ratio and hydrothermal treatment time on the formed mesostructure regularity has been studied. Different methods of template removal have also been evaluated. The samples were characterized by X-ray diffraction, nitrogen physisorption, FT-IR, and solid-state MAS NMR spectroscopy. 相似文献