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51.
In this research, Ni/SiO2 catalyst was modified with different amount of Gd2O3 and characterized with temperature-programmed desorption of CO2 (CO2-TPD) and NH3 (NH3-TPD), temperature-programmed reduction with H2 (H2-TPR) and X-ray diffraction (XRD). It was found that Gd2O3-modified Ni/SiO2 catalysts possessed higher CO2 adsorption and activation ability due to the formation of surface carbonate species. H2-TPR and XRD characterizations found that the strong interaction among nickel, Gd2O3 and SiO2 took place, which improved the dispersion of Ni. Gd2O3-modified Ni/SiO2 catalysts exhibited higher activity and stability for the combined oxy-CO2 reforming of methane in fluidized-bed reactor. The H2/CO ratio in produced syngas could be controlled via controlling reaction temperature and CO2/O2 ratio in feed. 相似文献
52.
丁辛醇装置丁醛加氢催化剂在装置扩能投产以后热点上移 (失活 )的速率较快 ,针对催化剂老化的原因进行分析、判断 ,找出原因 ,采用相应的解决措施 ,可延长催化剂使用寿命 ,增加装置效益 相似文献
53.
Stephan Boden Martina Bieberle Uwe Hampel 《Chemical engineering journal (Lausanne, Switzerland : 1996)》2008,139(2):351-362
Cone-beam type X-ray computed tomography (CBCT) is a potential method to measure three-dimensional phase distributions in vessels. An example for that is the measurement of gas profiles in stirred chemical reactors. Such data are highly valuable for the assessment and evaluation of chemical processes, for optimisation of the reactor and stirrer design, and for evaluation of computational fluid dynamics codes used to model the fluid flow and heat transfer in reactive systems. However, there are considerable difficulties for accurate quantitative measurements due to beam hardening and radiation scattering effects. In a theoretical and experimental work we have investigated the non-linear effects of both physical phenomena and developed a suitable measurement setup as well as calibration and software correction methods to achieve a highly accurate measurement of void fraction profiles with CBCT. 相似文献
54.
55.
乙烯裂解炉内传递和反应过程综合数值模拟Ⅱ.反应管内传递和反应过程的数值模拟 总被引:4,自引:0,他引:4
采用乙烯裂解炉传递反应过程综合数学模型中的反应管数学模型,对工业裂解炉反应管进行了系统的数值模拟,得到了反应管内流场、温度场和浓度场的详细信息,揭示了反应管内流动、传热、传质和裂解反应的基本特点。模拟结果表明,沿反应管轴向油气吸热升温,裂解反应加剧,产物产率逐渐发生变化;沿反应管径向存在明显的流体流速和温度的变化,而产物产率的变化不如流体流速和温度的变化明显。通过比较湍流粘度和分子粘度的大小,认为29.975~30mm的径向区域为层流层,层流层的存在使得临近管壁的区域内流体流速和温度变化显著。 相似文献
56.
The effects of H2O and NH3 on the kinetics of the liquid phase hydrogenation of tetralin to decalin at 6.9 MPa and 330°C over commercial P---Ni---Mo/alumina catalysts in the presence of H2S have been investigated. H2O functioned as a mild kinetic inhibitor to an extent sensitive to the H2S level. Quasi in situ XPS was used to investigate the catalyst structure after exposure to H20/H2S. 相似文献
57.
Adaptation of the microscopic properties of redox catalysts to the type of gas-solid reactor 总被引:1,自引:0,他引:1
Catalysts of selective oxidation usually work in a simultaneous redox mode in reactant/air cofed reactors. The solid must provide selective lattice oxygen according to a kinetic mechanism depending on operating conditions that differ from one reactor to another. Better catalytic performance can be obtained in a recirculating solids reactor because it allows separate optimization of the reduction and oxidation steps. Among the microscopic properties of the catalyst, the crystal morphology is to be taken into account because it influences its reactivity on stream. These considerations lead to a new approach of the catalyst-reaction-reactor trio. 相似文献
58.
本文主要完成了液态金属钠高温沸腾实验回路的应力分析与计算,确定了回路高温区连接管系的布置型式和支吊架系统,是该回路总体设计的重要组成部分。 相似文献
59.
A. Martin D. Gutschick N. I. Jaeger G. Schulz-Ekloff H. Miessner B. Lücke 《Catalysis Letters》1994,27(1-2):119-130
In situ FTIR spectroscopy has been applied to study the reason of the different selectivity behaviour of rhodium in the CO hydrogenation reaction in dependence on the different particle size. Several forms of molecularly adsorbed CO are observed, such as linearly- and bridgedbonded CO on metallic rhodium as well as dicarbonyl species with Rh(I) centres formed by oxidation of Rh(0) with protons in presence of CO. Furthermore, non-reactive formate, acetate, and carbonate species are produced as side products of the reaction. The higher selectivity to oxygenates, particularly to methanol, is explained by the existence of multiple-bonded CO present only on small rhodium crystallites. The multiple-bonded CO formed at low temperatures is converted at higher temperatures to the highly reactive formyl species, which is hydrogenated to methanol. 相似文献
60.