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991.
992.
993.
Xiaohong LI Jun AI Wenying LI Dongxiong LI 《Frontiers of Chemical Engineering in China》2010,4(4):476-480
A co-precipitation method was employed to prepare Ni/Al2O3-ZrO2, Co/Al2 O3-ZrO2 and Ni-Co/Al2O3-ZrO2 catalysts. Their properties were characterized by N2 adsorption (BET), thermogravimetric analysis (TGA), temperature-programmed reduction (TPR), temperature-programmed desorption
(CO2-TPD), and temperature-programmed surface reaction (CH4-TPSR and CO2-TPSR). Ni-Co/Al2O3-ZrO2 bimetallic catalyst has good performance in the reduction of active components Ni, Co and CO2 adsorption. Compared with mono-metallic catalyst, bimetallic catalyst could provide more active sites and CO2 adsorption sites (C + CO2 = 2CO) for the methane-reforming reaction, and a more appropriate force formed between active components and composite support
(SMSI) for the catalytic reaction. According to the CH4-CO2-TPSR, there were 80.9% and 81.5% higher CH4 and CO2 conversion over Ni-Co/Al2O3-ZrO2 catalyst, and its better resistance to carbon deposition, less than 0.5% of coke after 4 h reaction, was found by TGA. The
high activity and excellent anti-coking of the Ni-Co/Al2O3-ZrO2 catalyst were closely related to the synergy between Ni and Co active metal, the strong metal-support interaction and the
use of composite support. 相似文献
994.
采用直热法粉末触变成形工艺制备了SiCp体积分数为60%的SiCp/2024铝基复合材料,研究了成形压力对其孔隙率、抗弯强度、热膨胀系数的影响。结果表明,成形压力过大不利于提高复合材料的密度;成形压力为60 MPa时,复合材料的抗弯强度最大,为289.33MPa;随着成形压力增加,复合材料的热膨胀系数先增加后减小。在成形压力为60 MPa时,复合材料在200℃的热膨胀系数最小,为6.687×10^-6 K^-1。 相似文献
995.
Zhonghua Xiang Dapeng Cao Xiaohong Shao Wenchuan Wang Jianwei Zhang Weize Wu 《Chemical engineering science》2010,65(10):3140-3146
The Cu3(BTC)2 Metal—oragnic frameworks (MOFs) are synthesized by four different processes, i.e. solvothermal method (sample 1), microwave-assisted solvothermal method (sample 2), a combination of solvothermal method and supercritical carbon dioxide (Sc-CO2) activation (sample 3) and a combination of microwave-assisted solvothermal method and Sc-CO2 activation (sample 4). By comparing the N2 adsorption isotherms of the four samples, it is found that the sample 4 displays the greatest N2 uptake. Due to the best performance of sample 4 in N2 adsorption, we further study H2 adsorption in the sample 4. Results indicate that the excess and absolute hydrogen uptakes of this material reach 4.12 and 4.49 wt% at T=77 K and P=18 bar, respectively, which is the largest one among all these reports on Cu3(BTC)2 for H2 storage at the same condition. Therefore, it is believed that a combination of the two technologies of microwave-assisted method and supercritical Sc-CO2 activation provides a new approach for chemical engineers rapidly and efficiently preparing MOFs for high-capacity H2 storage. 相似文献
996.
Preparation and electrochemical performance of polyaniline-based carbon nanotubes as electrode material for supercapacitor 总被引:2,自引:0,他引:2
Nitrogen-containing carbon nanotubes (CNTs) with open end and low specific surface area were prepared via the carbonization of polyaniline (PANI) nanotubes synthesized by a rapidly mixed reaction. On the basis of analyzing the morphologies and structures of the original and carbonized PANI nanotubes, the electrochemical properties of PANI-based CNTs obtained at different temperatures as electrode materials for supercapacitors using 30 wt.% aqueous solution of KOH as electrolyte were investigated by galvanostatic charge/discharge and cyclic voltammetry. It was found that the carbonized PANI nanotubes at 700 °C exhibit high specific capacitance of 163 F g−1 at a current density of 0.1 A g−1 and excellent rate capability in KOH solution. Using X-ray photoelectron spectroscopy measurement the nitrogen state and content in PANI-CNTs were analysed, which could play important roles for the enhancement of electrochemical performance. When the appropriate content of nitrogen is present, the presence of pyrrole or pyridone and quaternary nitrogen is beneficial for the improvement of electron mobility and the wettability of electrode. 相似文献
997.
Werner E. G. Müller Prof. Dr. Xiaohong Wang Prof. Dr. Bärbel Sinha Dr. Matthias Wiens Dr. Heinz‐C. Schröder Prof. Dr. Klaus Peter Jochum Dr. 《Chembiochem : a European journal of chemical biology》2010,11(8):1077-1082
The giant basal spicules (GBS) from Monorhaphis chuni (Porifera [sponges], Hexactinellida) represent the largest biosilica structures on Earth and can reach lengths of 300 cm (diameter of 1.1 cm). The amorphous silica of the inorganic matrix is formed enzymatically by silicatein. During this process, the enzyme remains trapped inside the lamellar‐organized spicules. In order to localize the organic silicatein scaffold, the inside of a lamella has been analyzed by nano‐secondary ion mass spectrometry (NanoSIMS). It is shown that the GBSs are composed of around 245 concentrically arranged individual siliceous lamellae. These surround an internal siliceous axial cylinder. The lamellae adjacent to the cylinder are thicker (10–30 μm) than the more peripheral lamellae (2–10 μm). One lamella of a thickness of 18 μm has been selected for further analysis. This lamella itself is composed of three sublamellae with an individual thickness of 2–6 μm each, which are then further organized into three cylindrical slats (thickness: 1.6–1.8 μm). Other than the main lamellae, the sublamellae are not separated from each other by gaps. The element analysis of the sublamellae by NanoSIMS revealed that the siliceous matrix is embedded in an organic matrix that consists of up to 6–10 wt/% of C. The pattern of C distribution reflects a distinct zonation of the organic material within the solid intralamellar biosiliceous material. A growth model for the lamella starting from nanosized silica particles is proposed: During formation of a lamella nanosized silica particles fuse, through biosintering processes, to slats that build the individual sublamellae, which then finally form the lamellae. In turn, those lamellae may form the higher structural entity, the axial cylinder. 相似文献
998.
TiO2-Al2O3 mixed oxides with different compositions ranging from 40wt-% to 95wt-% of TiO2 were prepared by sol-gel method and impregnated with different amounts of VO x . Supports and catalysts were characterized by X-ray diffraction (XRD), physisorption, temperature preprogrammed reduction (H2-TPR), and ammonia temperature programmed desorption (NH3-TPD). TiO2 content in the support had obvious effect on the crystal structure, texture characteristic, acid property, and catalytic activity in dehydrogenation of ethylbenzene (EB) with carbon dioxide. The highest catalytic activity was acquired when the TiO2 content was 50 wt-%. 相似文献
999.
目的: 分析当归多糖对糖尿病神经病变(DPN)大鼠TLR4/MyD88/NF-κB通路抑制影响。方法: 选取SPF级Wistar雄性大鼠105只,随机选取15只作为正常组,剩余90只大鼠制备DPN模型,成功造模75只,随机分成5组,模型组、当归多糖低、中、高剂量组和阳性对照组,每组15只。模型组和正常组大鼠采用2 mL/100 g生理盐水灌胃,当归多糖低、中、高剂量组大鼠给予当归多糖药液灌胃,阳性对照组给予弥可保+二甲双胍溶液灌胃,每日给药体积均为2 mL/100 g。每天1次,连续灌胃10 d。给药3、10 d后检测大鼠机械缩足反应阈值(PWT)、热缩足反射潜伏期(PWL),末次给药后检测大鼠空腹血糖、血清丙二醛(MDA)、超氧化物歧化酶(SOD)、过氧化氢酶(CAT)活性、谷胱甘肽过氧化物酶(GSH-Px)、白细胞介素-6(IL-6)、髓鞘碱性蛋白(MBP)、TNF-α及C反应蛋白(CRP)含量,检测大鼠运动神经传导速度(MNCV)、感觉神经传导速度(SNCV),大鼠坐骨神经内核因子-κB(NF-κB) mRNA、髓样分子因子88(MyD88) mRNA及Toll样受体4(TLR4) mRNA表达。结果: 模型组及当归多糖低剂量组大鼠空腹血糖、MDA含量显著高于正常组,CAT、SOD及GSH-Px含量显著低于正常组,当归多糖中、高剂量组大鼠空腹血糖、MDA含量显著低于模型组、阳性对照组,CAT、SOD及GSH-Px含量显著高于模型组、阳性对照组,差异有统计学意义(P<0.05);模型组、当归多糖低剂量组大鼠血清IL-6、MBP、TNF-α及CRP含量均显著高于正常组,当归多糖中、高剂量组大鼠血清IL-6、MBP、TNF-α及CRP含量均显著低于模型组、阳性对照组,差异有统计学意义(P<0.05);模型组、当归多糖低剂量组大鼠NF-κB mRNA、MyD88 mRNA及TLR4 mRNA表达量均显著高于正常组,当归多糖中、高剂量组大鼠NF-κB mRNA、MyD88 mRNA及TLR4 mRNA表达量均显著低于模型组、阳性对照组,差异有统计学意义(P<0.05)。结论: 当归多糖可显著改善DPN大鼠的周围神经损伤状态,促进神经传导的恢复,其机制可能与阻断TLR4/MyD88/NF-κB信号路径的转导,降低炎性因子水平,减轻神经的氧化应激损伤有关。 相似文献
1000.