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91.
92.
塔河油区奥陶系原油的成熟度较高,且受生物严重降解.不同的生物标志化合物成熟度参数仅对有机质生成原油的不同阶段起到标尺作用,需优选既能较好地抗生物降解且适用于较宽的成熟度范围的指标来分析塔河油气运移的可能途径.三环萜烷/17α(H)-藿烷、重排甾烷/规则甾烷及Ts/(Ts+Tm)的比值是比较适用于塔河油区这种特殊性质的原油的生物标志化合物.根据研究,奥陶系原油油气存在两个注入通道,早期主要是由南向北方向运移,油气成熟度相对较低,成藏较早;晚期由东向西运移,原油成熟度相对于早期的较高,原油成藏稍晚. 相似文献
93.
94.
生烃化学动力学在川东北普光气田的应用 总被引:9,自引:2,他引:7
普光气田是四川盆地近期发现的规模最大、埋藏最深、资源丰度最高的气田。通过认识普光气田各个烃源岩层的贡献量、生烃关键期与构造演化的关系、油气成藏具体模式等,建立生烃化学动力学模型、标定参数,结合地区烃源岩参数和地史、热史资料,定量描述该地区的生烃过程及油裂解成气过程。认为:普光地区的主力烃源岩为下志留统泥岩;主要干酪根生油期为早二叠世末到早三叠世末期(距今286Ma至240Ma);主要干酪根生气期为中三叠世(距今240Ma至230Ma);主要气源是原油后期热裂解气,原油裂解成气的时间比较晚,主要油裂解成气期为早白垩世(距今144Ma至97.5Ma),从而决定了普光气田的成藏模式为“多期成藏,油气转化,晚期定位”。图2表3参33 相似文献
95.
非洲油气勘探区战略选择建议 总被引:8,自引:5,他引:3
非洲不同类型的沉积盆地主要可归纳为:古、中生代挠曲盆地,中、新生代大陆边缘断陷盆地,板内裂谷盆地和大陆边缘进积三角洲盆地。通过盆地油气成藏条件地质综合评价、不同勘探阶段的类比和最终勘探潜力分析,对非洲的沉积盆地进行了划分,在此基础上,总结出非洲油气勘探区选择应遵循的原则。对于油气勘探长期战略选区,原则上,优选低成本油气远景区,即使存在高风险,但亦可获得高回报;对于油气勘探中期发展策略选区,应该寻找地质条件好的油气资源区,投资中短期高利润项目;对于油气勘探中短期发展策略选区,一般应优选中低成本、低风险、低利润且短期能获得油气发现和勘探突破的有利油气勘探区。图1表3参5 相似文献
96.
Rinkenauer Gerhard; Osman Allen; Ulrich Rolf; Müller-Gethmann Hiltraut; Mattes Stefan 《Canadian Metallurgical Quarterly》2004,133(2):261
Lateralized readiness potentials (LRPs) were used to determine the stage(s) of reaction time (RT) responsible for speed-accuracy trade-offs (SATs). Speeded decisions based on several types of information were examined in 3 experiments, involving, respectively, a line discrimination task, lexical decisions, and an Erikson flanker task. Three levels of SAT were obtained in each experiment by adjusting response deadlines with an adaptive tracking algorithm. Speed stress affected the duration of RT stages both before and after the start of the LRP in all experiments. The latter effect cannot be explained by guessing strategies, by variations in response force, or as an indirect consequence of the pre-LRP effect. Contrary to most models, it suggests that SAT can occur at a late postdecisional stage. (PsycINFO Database Record (c) 2010 APA, all rights reserved) 相似文献
97.
Frank J. Owens 《Materials Letters》2007,61(10):1997-1999
Molecular orbital calculations of the ionization potential of single wall carbon nanotubes having donor NH2 and acceptor NO2 groups bonded to the side walls and ends and boron and nitrogen substituted for carbon show substantial increases in ionization potential compared to carbon nanotubes with no functional groups and no carbon substitutions. The presence of a carbon vacancy on the side wall also causes a substantial increase in the ionization potential. The effect of tube length on the ionization energy is also calculated. The calculations also suggest that at appropriate levels of boron and nitrogen doping the armchair carbon nanotubes could be high temperature organic ferromagnetic materials. 相似文献
98.
Electric charges at the surface of a passive stainless steel are generally considered as concentrated either in the passive film itself, or at the metal/passive film interface, or in the electrical double layer at the film solution interface. Rest potential time dependence after immersion of a passive surface in aqueous electrolytes suggests however that slow processes occur in the onset of the surface charge. Specific experiments, such as streaming potential measurements and electrochemical impedance spectroscopy in a thin electrolyte cell, were carried out for understanding better this phenomenon. An AISI 304 type austenitic stainless steel with polished or bright annealed surface finishes was immersed in NaCl aqueous solutions with various pH and chloride concentrations. The streaming potential time evolution shows two steps: a first rapid one (∼2 min) is attributed to the onset of the surface charge. The second step is much slower (approximately several hours) and possibly due to an interphase layer between the passive film and the solution. Following this idea, the whole kinetics is controlled by cation migration across the interphase when the pH is larger than the isoelectric pH (pHiep), while chloride ions are incorporated in the interphase when pH < pHiep. Impedance measurements allow determining both the kinetics of charge transport and the thin cell conductivity. When glass is used as reference material for the cell walls instead of stainless steel, the Nyquist plots show a high-frequency response. For stainless steel cell walls, a low-frequency response is observed, attributed to a slow charge reorganisation inside the interphase layer. The charge distribution at metal/electrolyte interface is discussed in terms of a gel-like layer which possibly takes place at the passive film/electrolyte interface. 相似文献
99.
Eleonora M. Ungureanu Liviu Birzan George Buica Enache Cristian 《Electrochimica acta》2006,52(3):794-803
The cyclic voltammetry behavior of a series of five 1-substituted azulenes has been investigated as well as the electrochemical chlorination of these compounds. In the case of azulene compounds containing electron withdrawing groups which have higher oxidation potentials than that of the chloride ion, the electrochemical chlorination led usually to 3-chloro derivatives. The electrochemical chlorination fails for azulenes with lower oxidation potentials. Additionally some polyhalogenated compounds were obtained by controlled potential electrolyses. The paper also discusses the reaction mechanism of the electrochemical halogenation of 1-substituted azulenes. 相似文献
100.
Mikhail Yu. Sinev Yurii P. Tulenin Olga V. Kalashnikova Viktor Yu. Bychkov Vladimir N. Korchak 《Catalysis Today》1996,32(1-4):157-162
The analysis of methane oxidation in a wide range of pressures (0.05–10 atm) demonstrates that the efficiency of CH3 radicals recombination is of great importance for high selectivity of C2 hydrocarbons formation. The relative efficiency of different “colliders” assisting the stabilization of exited C2H*6 molecules increases in the series: solid surface> Ar> He. The increase of the overall reaction rate upon increasing pressure of the inert gases in the case of catalysts having a higher surface area and more developed pore structure is likely due to the contribution of the surface-induced chain reaction in the volume of pores. 相似文献