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41.
唐宇慧 《组合机床与自动化加工技术》2004,(7):57-59
文章在建立理想边缘成像模型的基础上,分析研究了一般成像系统的点扩展函数与空间采样频率的关系及对图像边缘定位精度的影响,给出了边缘定位误差.同时,还分析研究了量化精度对图像边缘的移位影响,给出了移位误差.最后,给出了本文的分析研究在零件视觉精密检测的应用情况. 相似文献
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43.
磷氮阻燃腈纶结构性能及阻燃机理研究 总被引:5,自引:0,他引:5
研究了含磷酸二氢铵和脲复合阻燃剂的共混阻燃腈纶的结构和性能。研究表明,在纤维成形加工过程中,部分阻燃剂聚合生成聚磷酸铵和聚脲,阻燃剂以微粒状均匀分散并包埋在纤维内部;阻燃剂的加入使纤维高序区大分子间等距离排列的规整性和片状结构单元等距离平行排列的程度降低,热稳定性亦略有下降;但纤维的宏形态结构及物理机械性能没有明显变化;磷氮阻燃腈纶具有良好的阻燃性和阻燃耐久性,经碱洗20次、水洗30次后,阻燃剂的磷和氮的保留率分别高达82.9%和89.5%,纤维的LOI值仍在26%以上。 相似文献
44.
The extinction mechanism of a CH4/N2-air counterflow nonpremixed flame interacting with a single vortex was numerically studied. An augmented reduced mechanism was used to treat the CH4 oxidation reactions. The contribution of each term in the energy and the OH species equations were evaluated to investigate the unsteady extinction mechanism of nonpremixed flame. The flame temperature began to decrease due to the convection heat loss when the flame interacted with a vortex. The investigation of the radical behavior during the flame-vortex interaction process also provided useful information on the unsteady extinction mechanism. The OH radical concentration could be used as a good tracer of the state of the unsteady extinction of nonpremixed flame. The reduction mechanism of OH concentration was confirmed by analyzing the contribution of each term in the OH species equation. At initial stage of flame-vortex interaction, the OH production and consumption rates increased gradually, while the OH concentration was kept nearly constant. Near the extinction limit, the OH production rate decreased rapidly due to the low flame temperature, and the balance between the OH production and OH consumption by diffusion could not be maintained. The unsteady nonpremixed flame interacting with a vortex under the conditions of regime (V) shown in the spectral combustion diagram [Thévenin, D., Renard, P.H., Fiechtner, G.J., Gord, J.R., Rolon, J.C., 2000. Regimes of non-premixed flame-vortex interactions. Proceedings of the Combustion Institute 28, 2101-2108.] was finally extinguished due to low reactivity, which was induced by the low flame temperature. 相似文献
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46.
火焰原子吸收光谱法测定苋菜中8种矿物元素 总被引:5,自引:0,他引:5
用空气-乙炔火焰原子吸收光谱法对苋菜中钾、钙、镁、铁、锌、铜、锰、铅8种矿物元素进行了测定,对样品前处理方法、酸度、共存元素干扰及元素线性范围进行了实验。在选定的实验条件下,可以用火焰原子吸收光谱法对苋菜中8种元素进行分别测定,互不干扰。方法的相对标准偏差为0.08%~3.17%(n=5),加标回收率为91.5%~102%。 相似文献
47.
Tri(acryloyloxyethyl) phosphate (TAEP) was blended in different ratios with epoxy acrylate EB600 and polyurethane acrylate EB270 to obtain a series of UV curable flame retardant resins. The thermal degradation mechanisms of their cured films in air were studied by thermogravimetric analysis, in situ Fourier‐transform infrared spectroscopy, and direct pyrolysis/mass spectrometry measurements. The results showed that the phosphate group in TAEP first degraded to form poly(phosphoric acid) before the degradation of EB600. Then, the formed poly(phosphoric acid) effectively promoted the conversion of EB600 to form char, which prevented the sample from further burning. However, urethane group in EB270 degraded simultaneously with phosphate group in TAEP, leading to not effectively increase the conversion of EB270 to char during the thermal degradation. It was thus found that the addition of TAEP more effectively improved the thermal stability, flame retardance, and the char yield during combustion of EB600 than those of EB270. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 99: 3130–3137, 2006 相似文献
48.
49.
聚酰胺66的复配阻燃研究 总被引:3,自引:0,他引:3
采用35%磷-溴-锑复配阻燃体系对聚酰胺66进行阻燃,极限氧指数可提高到33.6%,达到UL94-V0级(1.6mm),且无熔融滴落。阻燃体系的添加会导致聚酰胺66力学性能的下降,但与无机阻燃体系相比较,磷-溴-锑复配阻燃体系对聚酰胺66的力学性能影响较小。采用扫描电镜观察阻燃剂在聚酰胺66中的分散效果,发现分散均匀的体系,在水中或者在110℃的析出实验条件下,阻燃剂的析出量很小,可以维持较长时间的阻燃效果。 相似文献
50.
A series of phosphorus‐containing, wholly aromatic thermotropic copolyesters from acetylated 2‐(6‐oxide‐6H‐dibenz〈c,e〉〈1,2〉oxa phosphorin‐6‐yl)‐1,4‐dihydroxy phenylene, p‐acetoxybenzoic acid, terephthalic acid, and isophthalic acid were prepared by melting polycondensation. The structure and basic properties of the polymers, such as the glass‐transition temperature (Tg), melting temperature (Tm), thermal stability, crystallinity, and liquid crystallinity, were investigated with Fourier transform infrared, elemental analysis, differential scanning calorimetry (DSC), thermogravimetric analysis, wide‐angle X‐ray diffraction, and hot‐stage polarizing optical microscopy. The copolyesters had relatively high Tg values ranging from 183 to 192°C. The Tm values obtained from DSC curves for samples P‐20 and P‐25 were 290 and 287°C, respectively (where the number in the sample name indicates the molar fraction of the phosphorus‐containing monomer in the reactants). The initial flow temperatures of other samples observed with hot‐stage polarizing microscopy were 271–290°C. The 5% degradation temperatures in nitrogen ranged from 431 to 462°C, and the char yields at 640°C were 41–52%. All the copolyesters, except P‐40, were thermotropic and nematic. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 1278–1284, 2002 相似文献