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1.
三聚硫氰酸单钠盐是一种新型的多官能团化精细化学品。介绍了三聚硫氰酸单钠盐的制备方法,以及其在橡胶硫化、橡胶与金属的硫化粘合等领域的应用研究进展。  相似文献   
2.
As a new advanced oxidation technology, photocatalytic technology has broad application prospects in the field of wastewater treatment. However, in the actual use process, there will be difficulties in catalyst recovery and reuse. This article successfully prepared bacterial cellulose (BC) loaded silver and titanium dioxide nanoparticles (Ag-plated TiO2/BC composite pellicle) by in situ embedding method. BC not only works as the carrier to load TiO2 and Ag NPs but also adsorbs dyes to promote the reaction. As a reusable photocatalytic film, it is convenient to use and recycle in terms of testing and characterization compared with powders. The results show that Ag and TiO2 nanoparticles were closely embedded in BC. We evaluated the photocatalytic degradation performance of the catalyst on methylene blue (MB), active red X-3B, and Rhodamine B. When the reaction time was 2 h, the dye removal rates were 71%, 68%, and 82.6%. At the same time, through the inhibition zone experiment, it was found that the material has a certain inhibitory effect on both Escherichia coli and Staphylococcus aureus. Therefore, the supported catalyst prepared by this method has the advantages of high catalytic activity, relatively stable property, easy recovery, and tailorability, making it potentially applicable in sewage post-treatment links.  相似文献   
3.
采用Ni-P复合改性HZSM-5催化剂催化木质素降解制备高附加值的单酚类化学品,探讨了催化剂种类、金属负载量、反应温度、反应时间以及溶剂种类对木质素催化降解制备酚类化合物的影响。同时采用X射线衍射仪(XRD)、比表面积和孔径分析仪(BET)、化学吸附仪(NH3-TPD)、热重分析仪(TG)以及气相色谱质谱联用仪(GC/MS)对催化剂以及液相产物进行分析表征,同时探讨其催化失活以及再生机制。结果表明:Ni、P高度分散在HZSM-5催化剂的表面,Ni的添加有效地弱化了C-C键,致使β-O-4和α-O-4发生断裂,有效地提高了木质素加氢解聚的活性,减少了焦炭的生成,但催化剂的再生水热稳定性较差,重复使用性较低。当采用甲醇为供氢试剂,在反应温度为220℃,氢气压力为2MPa,反应时间为8h,催化剂负载量为10%,NaOH为共催化剂时,其木质素的转化率为98.6%,酚类化合物的含量达到74.97%。产物以苯酚、愈创木酚和紫丁香酚为主,低温促进了紫丁香酚的产生。  相似文献   
4.
针对镀液温度变化的非线性和滞后性,设计了采用专家规则的镀液温度实时控制系统。该系统在实时监测的基础上,构建了综合评判镀液温度偏差和镀液温度偏差变化率的专家规则,实现了镀液温度的自适应快速调节。仿真分析结果表明,该系统克服了非线性和滞后性的不良影响,能够实现镀液温度的实时控制。  相似文献   
5.
《Ceramics International》2021,47(18):25287-25295
The presence of SiC nanoparticles within the Graphene oxide (GO) incorporated electroless deposited NiP layers (NiP-GO) on carbon steel substrate was studied in this work. The effect of co-deposition of GO nanoplatelets and/or SiC nanoparticles on the morphology and structure of the heat-treated NiP coatings were investigated by scanning electron microscope and X-ray diffraction, respectively. The results revealed that the heat-treated NiP and NiP–SiC coatings consisted of Ni and Ni3P phases, whereas the NiP-GO also contains the intermediated Ni2P and Ni12P5 metastable phases due to the incomplete precipitation of Ni3P. Such metastable phases are significantly decreased by the incorporation of SiC nanoparticles in NiP-GO coatings. The mechanical properties of the coatings were characterized by microhardness measurement and “pin on disk” wear test. The corrosion tests were conducted in aqueous 3.5 %wt NaCl using electrochemical measurement for Ni–P, NiP-GO, NiP–SiC, and NiP-GO-xSiC coatings. By co-deposition of SiC nanoparticles, the hardness of NiP-GO is significantly increased and the wear loss is reduced, especially at a high sliding distance during the wear test. The corrosion behavior of the NiP-GO coatings containing different amounts of SiC nanoparticles has been investigated.  相似文献   
6.
This work demonstrates a facile Nb2O5-decorated electrocatalyst to prepare cost-effective Ni–Fe–P–Nb2O5/NF and compared HER & OER performance in alkaline media. The prepared electrocatalyst presented an outstanding electrocatalytic performance towards hydrogen evolution reaction, which required a quite low overpotential of 39.05 mV at the current density of ?10 mA cm?2 in 1 M KOH electrolyte. Moreover, the Ni–Fe–P–Nb2O5/NF catalyst also has excellent oxygen evolution efficiency, which needs only 322 mV to reach the current density of 50 mA cm?2. Furthermore, its electrocatalytic performance towards overall water splitting worked as both cathode and anode achieved a quite low potential of 1.56 V (10 mA cm?2).  相似文献   
7.
Thermal and mechanical resistances of palladium composite membranes prepared by Electroless Pore-Plating (ELP-PP) and containing SBA-15 as intermediate layer were improved by doping the silica material with Pd nuclei before its incorporation on the composite membrane. Textural properties of synthesized SBA-15 materials (both raw and doped ones) were analyzed by XRD, N2 adsorption-desorption at 77 K and TEM, while the main properties of the composite membrane were determined by SEM and gravimetric analyses. Moreover, membrane permeation tests were also carried out with pure gases, hydrogen and nitrogen, and binary mixtures of them at temperature of 400 °C and pressure driving forces in the range of 0.5–2.5 bar. The use of bare SBA-15 intermediate layer leads to the appearance of cracks on the Pd layer during permeation experiments at high temperature. In contrast, the use of Pd-doped SBA-15 particles avoids this problem, thus improving both thermal and mechanical resistances of the composite ELP-PP Pd-membrane. Following this preparation method, an estimated Pd thickness of 7.1 μm was obtained, reaching a hydrogen permeance of 3.81·10?4 mol s?1 m?2 Pa?0.5 and ensuring an ideal H2/N2 separation factor higher than 2550 at 400 °C.  相似文献   
8.
Substrate surface modification is a key pretreatment during fabrication of composite palladium membranes for hydrogen purification in hydrogen energy applications. The suspension of a natural porous material, Nontronite-15A mineral, without any organic additives was employed in dip-coating of the porous Al2O3 substrate. The Nontronite-15A mineral was characterized by SEM, XRD, TG−DSC and granulometry analysis. The surface and cross-section of the coated porous Al2O3 tubes were observed by SEM, and their pore size distribution and nitrogen flux were also measured. Palladium membranes were fabricated over the coated Al2O3 tubes by a suction-assisted electroless plating. The optimal loading amount of the Nontronite-15A mineral is just to fill in and level up the surface cavities of the Al2O3 substrate rather than to form an extra continuous layer. A thin and selective palladium membrane was successfully obtained, and its permeation performances were tested. The kinetic analyses on the hydrogen flux indicate that the hydrogen permeation behavior exhibits typical characteristics for most of the palladium membranes. During the stability test at 450 °C for 192 h, no membrane damage was detected, and the hydrogen flux increased slightly.  相似文献   
9.
ABSTRACT

In the present paper, the mechanical properties and the scratch failure mechanisms of Ni–P electroless coatings are described. The material microstructure was studied in as-deposited and annealed conditions through SEM and EDS analyses. Nanoindentation measurements on the coatings showed a remarkable hardening due to the crystallization and precipitation behaviour produced by annealing. The scratch tests, conducted by increasing the load during scratch, revealed the coating failure mechanisms in a broad range of applied stresses up to delamination.  相似文献   
10.
Surface oxidation of the in-flight powders during the preparation of amorphous coatings in high velocity oxygen fuel process causes the formation of oxygen-rich intersplat regions. These regions are brittle in nature and can dramatically deteriorate the mechanical performance of the coatings. To solve this problem, the starting FeCrMoCBY amorphous feedstock powders were modified by electroless plating a thin layer of Ni–W–P amorphous phase. It was found that the covering of the Ni–W–P layer can significantly reduce the oxygen content in the resultant Fe-based amorphous coatings. The wear resistance of the coatings with and without the modification of Ni–W–P thin layer was comparatively studied by ball-on-disk wear tests against Si3N4 counterpart in air. It revealed that the wear of two types of coatings follows the same oxidation wear mechanism but the modified coating exhibits much better wear resistance due to the improved oxidation resistance.  相似文献   
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