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981.
炭黑对轮胎胎面胶热物性的影响 总被引:1,自引:0,他引:1
研究了炭黑品种和用量对轮胎胎面胶热扩散系数(α)、导热系数(λ)及比热容(C)3种热物性参数的影响规律。结果表明,随着炭黑填充量的增加,胎面胶的α及λ均逐渐增大,C逐渐减小。炭黑的结构性对胎面胶α的影响程度大于炭黑的粒径;温度相同时,炭黑的结构性越高,其填充胎面胶的α越大;随着炭黑填充量的增加,3种炭黑填充胎面胶α之间的差距呈现先增大后减小的变化趋势。炭黑的结构性及粒径对胎面胶C的影响没有固定的规律,但在低温区,炭黑的粒径越大,其填充胎面胶的C越大,且炭黑填充量对此差距无影响。炭黑的结构性对胎面胶λ的影响程度大于炭黑的粒径;温度相同时,炭黑的结构性越高,其填充胎面胶的λ越大;当炭黑用量较低时,其对胎面胶λ的影响程度相对较小,随着炭黑填充量的增加,3种炭黑填充胎面胶λ之间的差距呈现先增大后减小的变化趋势。 相似文献
982.
A wireless sensor network (WSN) commonly whilst a body sensor network (BSN) must be secured with requires lower level security for public information gathering, strong authenticity to protect personal health information. In this paper, some practical problems with the message authentication codes (MACs), which were proposed in the popular security architectures for WSNs, are reconsidered. The analysis shows that the recommended MACs for WSNs, e.g., CBC- MAC (TinySec), OCB-MAC (MiniSec), and XCBC-MAC (SenSee), might not be exactly suitable for BSNs. Particularly an existential forgery attack is elaborated on XCBC-MAC. Considering the hardware limitations of BSNs, we propose a new family of tunable lightweight MAC based on the PRESENT block cipher. The first scheme, which is named TukP, is a new lightweight MAC with 64-bit output range. The second scheme, which is named TuLP-128, is a 128-bit variant which provides a higher resistance against internal collisions. Compared with the existing schemes, our lightweight MACs are both time and resource efficient on hardware-constrained devices. 相似文献
983.
984.
UASB-SBR工艺处理啤酒废水 总被引:1,自引:0,他引:1
阐述了UASB-SBR组合工艺处理啤酒废水的工艺流程,实践表明,UASB-SBR系统具有运行稳定、费用低、抗冲击负荷强等优点。 相似文献
985.
Boron-based metal-free catalysts for oxidative dehydrogenation of propane (ODHP) have drawn great attention in both academia and industry due to their impressive activity and olefin selectivity. Herein, the SiO2 and B2O3 sequentially coated honeycomb cordierite catalyst is designed by a two-step wash-coat method with different B2O3 loadings (0.1%-10%) and calcination temperatures (600, 700, 800 ℃). SiO2 obtained by TEOS hydrolysis acts as a media layer to bridge the cordierite substrate and boron oxide via abundant Si-OH groups. The welldeveloped straight channels of honeycomb cordierite make it possible to carry out the reactor under high gas hourly space velocity (GHSV) and the thin wash-coated B2O3 layer can effectively facilitate the pore diffusion on the catalyst. The prepared B2O3/SiO2@HC monolithic catalyst exhibits good catalytic performance at low boron oxide loading and achieves excellent propylene selectivity (86.0%), olefin selectivity (97.6%, propylene and ethylene) and negligible CO2 (0.1%) at 16.9% propane conversion under high GHSV of 345,600 ml·(g B2O3)-1·h-1, leading to a high propylene space time yield of 15.7 g C3H6·(g B2O3)-1·h-1 by suppressing the overoxidation. The obtained results strongly indicate that the boron-based monolithic catalyst can be properly fabricated to warrant the high activity and high throughput with its high gas/surface ratio and straight channels. 相似文献
986.
Acetylene as a reducing agent for the selective catalytic reduction (C2H2-SCR) of NO in the presence of excess oxygen on various Ce-exchanged zeolites was investigated for the first time. Under the conditions of 1600 ppm NO, 800 ppm C2H2, and 9.95 % O2 in He, the Ce-H-ZSM-5 (Si/Al=25) catalyst shows about 83% NO conversion to N2 at the temperatures ranged from 300 to 350 °C. It is followed by the other zeolites in the activity order of Ce-H-Y (Si/Al=2.5), Ce-H-_ (Si/A1=20∼30), and Ce-H-SAPO (Si/Al=34), Ce-H-5A (Si/Al=12). Almost no NO conversion was obtained over Ce-Na-ZSM-5 (Si/Al=25) and Na-ZSM-5 (Si/Al=25) catalyst samples. The Conversion of NO to N2 increased with O2 concentration in the range of 0.1 ∼ 9.95% over the CeH-ZSM-5 (Si/Al=25) catalyst. It is suggested that O2 plays an important role in the C2H2-SCR of NO reaction, by oxidizing NO to NO2 on acid sites in assistant with cerium species of the catalyst. A large amount of CO, which seems to be in proportion with the NO conversion to N2, was produced. Long-term experiments up to 56 h combined with a excursion of the reaction temperature up to 650 °C over the Ce-H-ZSM-5 (Si/A1=25) confirmed the catalyst’s durable performance under the reaction conditions. It is found that the de-NOx activity of Ce-H-ZSM-5 catalyst can be enhanced by the presence of 50 ppm of sulfur dioxide in the dry-feed reaction conditions. 相似文献
987.
硅烷/聚硅氧烷化学改性双酚A型环氧树脂研究 总被引:6,自引:0,他引:6
提出了一种有机硅改性电子封装用双酚A型环氧树脂新方法——用二氯二甲基硅烷(DMS)或其与。α,ω-二氯聚二甲基硅氧烷(DPS)的混合物来改性双酚A型环氧树脂;测定了固化物的冲击强度、拉伸强度、断裂伸长率、玻璃化转变温度等;用扫描电子显微镜观察了改性材料的断面形态。结果表明,环氧树脂经5.7份DMS或0.7份DMS、10份DPS改性后,均达到了很好的增韧和提高耐热性等效果,符合电子封装材料改性要求;后者的增韧效果更为显著,其断面SEM照片呈现特殊的褶皱状微团结构。 相似文献
988.
End amino, carboxylic acid, and hydroxyl functionalized styrene–butadiene–styrene (SBS) triblock copolymers were prepared with 1,5‐diazabicyclo[3.1.0]hexane, carbon dioxide, and epoxy ethane as capping agents, respectively. The effects of the end polar groups on the morphology and dynamic mechanical properties were investigated. Transmission electron microscopy images suggested that the group at the end of the polystyrene (PS) segment made the morphology of the PS domains disordered and incompact. Dynamic mechanical results showed that the storage and loss modulus increased after SBS was end‐functionalized. End amino and carboxylic acid groups improved the compatibility and storage stability of SBS‐modified asphalt. However, the effect of the end‐hydroxyl group on the improvement of the storage stability of SBS‐modified asphalt was not obvious. The differential scanning calorimetry analysis of SBS‐modified asphalt further showed that the compatibility and storage stability of SBS‐modified asphalt were improved by the attachment of amino or carboxylic acid groups through the anionic polymerization method. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 8–16, 2007 相似文献
989.
Equipped with 512-bit wide SIMD instructions and large numbers of computing cores, the emerging x86-based Intelr Many Integrated Core (MIC) Architecture provides not only high floating-point performanc... 相似文献
990.
Calcium carbonate/natural rubber (NR) latex nanometer composites were prepared by adding nanometer CaCO3 whose surface had been treated to natural rubber latex (NRL) before sulfuration. The physical, thermooxidative aging, and thermal degradation properties and the ultra‐microstructure were analyzed with a multipurpose material testing meter, a thermal analysis meter and a Philips XL‐30 SEM, respectively. The results showed that the structures and properties of nanometer composites could be clearly improved by NRL mixed with surface‐treated nanometer CaCO3. The physical properties of the nanometer composites were best when the content of surface treatment agent was 2.5% (to nanometer CaCO3), the nanometer CaCO3/NRL content was 3:100, and the stirring time for treating the surface of the nanometer CaCO3 was 20 min. Simultaneously, the thermooxidative aging resistance of the nanometer composites also was significantly improved. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 3442–3447, 2006 相似文献