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231.
The partition coefficients of ethylene between hydrate and vapor for methane + ethylene + water and methane + ethylene + SDS + water systems 总被引:1,自引:0,他引:1
The hydrate formation of CH4+C2H4 mixture was studied experimentally in two different cases, with and without the presence of sodium dodecyl sulfate (SDS) in water. The results manifested that the presence of SDS could not only accelerate the hydrate formation process, but also increase the partition coefficient of ethylene between hydrate and vapor drastically. The partition coefficients of ethylene between hydrate and vapor for methane + ethylene + water with the presence of 500 ppm SDS in water were then systematically measured. The experimental temperature ranged from 273.15 to 278.15 K, the pressure ranged from 2.5 to 5.5 MPa, the initial gas-liquid volume ratio ranged from 95 to 240 standard volumes of gas per volume of liquid, and the mole percentage of ethylene in feed gas mixture ranged from 5.28% to 79.36%. The results demonstrated that ethylene could be enriched in hydrate phase and partition coefficients were increased with the presence of SDS in water. This conclusion is of industrial significance; it implies that it is feasible to recover ethylene from gas mixture, e.g., various kinds of refinery gases or cracking gases in ethylene plant, by forming hydrate. 相似文献
232.
Electrolytic recovery of chlorine from hydrogen chloride gas with fused molten salt electrolyte LiCl/KCl 总被引:1,自引:0,他引:1
A method of electrolytic recovery of chlorine from hydrogen chloride gas based on the fused molten salt LiCl/KCl is under development. For the feasibility study, described here, a reticulated vitreous carbon (or porous carbon) cathode was immersed in a low-melting eutectic of LiCl/KCl. A graphite rod was used as the anode. Gaseous dilute hydrogen chloride, in a mixture with nitrogen, was reduced to elemental hydrogen and chloride at the cathode, and chlorine was produced at the anode. At stoichiometric current, current efficiency is greater than 90%. The removal efficiency is as high as 97%.Patent pending (May 1995). 相似文献
233.
酯交换法合成碳酸二苯酯研究进展 总被引:4,自引:0,他引:4
对碳酸二苯酯合成用催化剂、合成工艺、反应装置等进行了综述。认为国内应加强酯交换法合成碳酸二苯酯的基础研究 ,尽快实现其产业化 相似文献
234.
235.
Steven Swier Yong Sung Chun Jeffrey Gasa Montgomery T. Shaw R.A. Weiss 《Polymer Engineering and Science》2005,45(8):1081-1091
Sulfonated poly(ether ketone ketone) ionomers (SPEKK) with ion‐exchange capacities (IEC) between 0.2 and 3.4 meq/g were prepared by sulfonating PEKK with a mixture of concentrated and fuming sulfuric acids. Sulfonation occurs only on the phenyl rings attached to ether and ketone groups. The glass transition temperature of the dry SPEKK ionomers increased linearly with increasing IEC, and the ionomers were thermally stable to ~250°C, above which desulfonation occurred. Water‐swollen ionomers exhibited microphase separated morphologies, and the average correlation length determined by small angle X‐ray scattering increased with increasing IEC. The proton conductivity of hydrated SPEKK membranes measured by impedance spectroscopy ranged from ~10–3 to 10–1 S/cm as the IEC increased from ~1.0 to 2.4 meq/g. Single cell performance curves on membrane‐electrode assemblies (MEA) indicated that the SPEKK membranes approached the performance of Nafion? for an IEC of 2 meq/g. POLYM. ENG. SCI., 45:1081–1091, 2005. © 2005 Society of Plastics Engineers 相似文献
236.
介绍了国外利用天然气生产油口的生产工艺,探讨了山西省利用丰富的煤层气资源发展合成油的可能性和优势,并提出了相应的发展建议。 相似文献
237.
Hyoun-Ee Kim Steven J. Zinkle William R. Allen 《Journal of the American Ceramic Society》1990,73(2):425-429
Alumina enriched in 17 O was successfully fabricated from aluminum isopropoxide and water containing the 17 O isotope. This material was necessary for an experiment to study the radiation damage expected in alumina exposed to a nuclear fusion reactor environment. The enrichment levels of specimens subjected to different preparation schedules were measured using a nuclear reaction analysis technique. Replacement of the 17 O isotope in the ceramic by atmospheric oxygen occurred readily. Therefore, successful fabrication of suitably enriched alumina specimens required that all processing steps be performed under vacuum or inertgas environments. The optimum fabrication procedure produced enriched alumina specimens of >99.5% of theoretical density, ∽10-μm grain size, and a flexural strength of 280 MPa. 相似文献
238.
Reed M. Izatt Steven R. Izatt Don W. Mcbride Jr. Jerald S. Bradshaw James J. Christensen 《Israel journal of chemistry》1985,25(1):27-32
Macrocycle-mediated fluxes of Cd(NO3)2 and of several binary mixtures of Cd(NO3)2 with the nitrate salt of either Na+, K+, Rb+ Cs+, Ag+, Ca2+, Sr2+, Pb2+, Zn2+, or Cu2+ have been determined in a H2O-CHCl3–H2O liquid membrane system. Of the macrocycles studied, 2.2 and 2.2DD most successfully transported Cd2+ In the Cd2+–Mn+ mixtures, Cd2+ was transported selectively with 2.2 when Mn+ was either an alkali or an alkaline earth cation. However, when Mn+ was either Ag+, Pb2+, or Cu2+ the Cd2+ flux was reduced sharply. Generally, cation flux was greater for 2.2DD than for 2.2 with selectivity for Cd2+ being altered also in several cases. Relative fluxes from binary cation mixtures depend on metal cation radius, macrocycle cavity diameter, ligand ring substituent and log K for metal ion-macrocycle interaction. 相似文献
239.
本文介绍了一种特殊的高转速、无稳心搅拌系统,具备简洁、高效、稳定、安全的特点,经使用证明,效果良好,性能可靠,为高速搅拌及无稳心反应釜的应用提供了一条新的设计及运用的途径。 相似文献
240.
Shampa Kandoi Jeff Greeley Marco A. Sanchez-Castillo Steven T. Evans Amit A. Gokhale James A. Dumesic Manos Mavrikakis 《Topics in Catalysis》2006,37(1):17-28
A microkinetic model for methanol decomposition on platinum is presented. The model incorporates competitive decomposition
pathways, beginning with both O–H and C–H bond scission in methanol, and uses results from density functional theory (DFT)
calculations [Greeley and Mavrikakis, J. Am. Chem. Soc. 124 (2002) 7193, Greeley and Mavrikakis, J. Am. Chem. Soc. 126 (2004)
3910]. Results from reaction kinetics experiments show that the rate of H2 production increases with increasing temperature and methanol concentration in the feed and is only nominally affected by
the presence of CO or H2 with methanol. The model, based on the values of binding energies, pre-exponential factors and activation energy barriers
derived from first principles calculations, accurately predicts experimental reaction rates and orders. The model also gives
insight into the most favorable reaction pathway, the rate-limiting step, the apparent activation energy, coverages, and the
effects of pressure. It is found that the pathway beginning with the C–H bond scission (CH3OH→H2COH→HCOH→CO) is dominant compared with the path beginning with O–H bond scission. The cleavage of the first C–H bond in methanol
is the rate-controlling step. The surface is highly poisoned by CO, whereas COH appears to be a spectator species. 相似文献