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51.
大学生求学满意度实证研究--某高校学生个体特征对满意度单项要素的影响分析 总被引:1,自引:0,他引:1
求学满意度,又称为求学满意程度,它取决于教育需求主体对教育服务的预期同其实际所感知的教育服务水平的对比。教学计划、教学组织、教师教学、教学设施、校园环境、学生5知识技能等都是影响求学满意度的因素。本文在调查取得基本数据的基础上,使用相关的统计检验方法,分析了性别、生源地和不同年级这些学生个体地征对求学满意度单项要素的影响。主要结论有:学生性别差异对满意度单项要素的影响基本是随机的;不同生源地的学生对教学计划和管理制度两个要素的评价具有差异;不同年级的学生对教学设施和知识掌握程度的评价具有显著性差异;学生对学校服务评价单项因素差异很少,总体满意度在一定程度上反应学校的实际情况。 相似文献
52.
针对单机架可逆式冷轧机生产过程中,由于不同热轧生产厂的热轧板形原料性能、板形差别较大、从而造成弯辊力预设定值和实际指标相差较大的问题,利用现场生产工艺数据丰富,采用人工智能BP神经网络的方法,通过大量数据输入进行训练,大大的提高了生产过程中弯辊力预设定值的准确性。 相似文献
53.
从应变范围区分法(SRP),应变能区分法(SEP)的有关概念出发,研究DD3单晶镍基合金拉—拉应力状态下的蠕变—疲劳性能和保持时间的影响,并对其进行了定量计算;同时,用应变能区分法的数值法(SEP—NCM)实现对拉—拉应力状态下蠕变—疲劳的寿命预测。 相似文献
54.
The residual stresses in -Al2O3 scales formed on high-purity FeCrAl and FeCrAlY during oxidation at 1200°C and subsequent cooling and reheating were studied using photostimulated luminescence spectroscopy. Systematic measurements of the stress in the oxide were made as a function of both alloy thickness and cooling rate and the development of stresses in the oxide scale during thermal cycling was investigated as a function of the temperature. Depending on the ratio of the alloy and oxide-scale thicknesses, substantial stress relaxation was observed to occur during cooling at a rate of 8 K/min. Compressive growth stresses of 1 GPa were determined by comparing the residual-stress measurements at room temperature with those calculated based on thermal-expansion mismatch. No significant differences in the growth stresses, the total residual stresses, or the stress relaxation during thermal cycling were observed between the oxides formed on the Y-doped and undoped FeCrAl samples. Stress relaxation is also shown to lead to the development of tensile stresses in the oxide scale under certain conditions, in particular, those associated with slow cooling followed by rapid heating. 相似文献
55.
冷镦挤复合的连接成形工艺分析及模具设计 总被引:2,自引:0,他引:2
基于镦挤连接成形的金属塑性变形规律,分析了一次连接成形件的冷镦挤复合成形的形变特点和工艺特点,进行了冷镦挤一次连接成形工艺过程的可行性分析设计和模具设计,并得到了生产实践验证。 相似文献
56.
针对在塑料挤出过程中温度控制的重要性,介绍了一种新型的PID温度控制系统。该系统采用高性能单片机芯片,可以方便地对系统加热、冷却周期及PID的各个参数进行在线设定和修改,提高了塑料挤出机的温控精度。 相似文献
57.
In order to analyse iron phosphate complexes and gel-like phases encountered in the single superphosphate process, experiments were performed with a free-Al, Fe apatite crystal of Durango from Mexico phosphate rock and sulfuric acid. Reaction products were studied by X-ray diffraction and surface analysis methods namely X-ray photoelectron spectroscopy and scanning electron microscopy. Results show that in a free Al, Fe-system, part of the Ca(H2PO4 )2.H2O (MCPM) forms before precipitation of any CaSO4(CS) and gel-like phase such H2SO4.yH3PO4.xH2O is formed. When iron is added, the precipitation rate of (CS) and (MCPM) increases and Fe3(H3O)H8(PO4)6.6H2O is formed. When Fe and Al are added, a gel-like phase is quickly formed with a molar ratio that changes with time and develops into crystalline compounds. The composition of this gel may be represented as a mixture of two phases: H2SO4.yH3PO4.xH2O and a gel containing Al-Fe-Si. 相似文献
58.
由于绿原化工有限公司过磷酸钙装置生产能力由 6 70 t/ d(实物量 )提高到 84 0 t/ d,折流混合器负荷增大 ,出现折流环磨损加快等问题。采用若干技改措施 :扩大折流环内径、改变折流混合器喷射方向、采用新材料制作折流环 ,使折流混合器能满足 84 0 t/ d过磷酸钙生产的需要 相似文献
59.
Polystyrene (PS)/poly(ethylene oxide) (PEO) prototype brushes were prepared by alternating free‐radical copolymerization of methacryloyl‐terminated PS and α‐vinylbenzyl‐ω‐hydroxy or α‐vinylbenzyl‐ω‐perfluoroalkyl (Rf) PEO macromonomers with the addition of Lewis acid (SnCl4). It was found from their dilute‐solution properties that PS/PEO end‐capped with Rf (PBRf), and PS/PEO having OH groups at terminal ends (PBOH) prototype brushes formed a single molecule in benzene and aggregates in chloroform, respectively. However, the brush PBOH formed a single molecule in N,N‐dimethylformamide. Such aggregation behaviors seemed to be caused by the interaction between hydroxy groups of PEO chain ends. The brush PBOH was also converted into PBRf‐type brush by chemical modification, using corresponding acid chloride. The substitution of Rf groups was ~70% due to slipping of terminal hydroxy groups into PEO internal domains. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 772–778, 2006 相似文献
60.
The electrochemical reduction of nitrate ion was studied by cyclic voltammetry on Pt(1 1 1) and [n(1 1 1) × (1 1 1)] stepped Pt surfaces, where n (=14, 10, 7, 6, 5, 4, 3, 2) is the number of terrace atoms, in 0.1 M HClO4 + 10 mM KNO3. The electrocatalytic nitrate reduction was found to hardly proceed on Pt(1 1 1) in the hydrogen adsorption region, while the electrocatalytic activity was improved with the increase in the step density. Inactivation was observed in the presence of adsorbed hydrogen or nitrate-derived reduced adsorbate, i.e. adsorbed NO, on (1 1 1) step sites. It was, therefore, concluded that the electrocatalytically active NO3− species does not adsorb on the (1 1 1) terraces but on the (1 1 1) monoatomic steps. The nitrate reduction current increased with the step density in a non-linear relationship. The overall current density at 0.21 V (RHE) corresponding to the peak potential of the main electrocatalytic nitrate reduction wave which was maximum at n = 2, abruptly increased with short terraces, i.e. n < 5, where the current wave of adsorbed hydrogen on the Pt stepped surface with comparatively narrow (1 1 1) terraces, denoted as Hnt, also appeared unmodified for n < 5 on voltammograms recorded in 0.1 M HClO4 in the absence of nitrate. 相似文献