全文获取类型
收费全文 | 78321篇 |
免费 | 7122篇 |
国内免费 | 5427篇 |
专业分类
电工技术 | 2606篇 |
技术理论 | 2篇 |
综合类 | 7050篇 |
化学工业 | 26550篇 |
金属工艺 | 5713篇 |
机械仪表 | 6024篇 |
建筑科学 | 4096篇 |
矿业工程 | 2613篇 |
能源动力 | 1792篇 |
轻工业 | 4265篇 |
水利工程 | 1068篇 |
石油天然气 | 4664篇 |
武器工业 | 1011篇 |
无线电 | 3919篇 |
一般工业技术 | 9424篇 |
冶金工业 | 2342篇 |
原子能技术 | 411篇 |
自动化技术 | 7320篇 |
出版年
2024年 | 573篇 |
2023年 | 1759篇 |
2022年 | 2938篇 |
2021年 | 3114篇 |
2020年 | 2587篇 |
2019年 | 2118篇 |
2018年 | 2007篇 |
2017年 | 2276篇 |
2016年 | 2579篇 |
2015年 | 2602篇 |
2014年 | 3985篇 |
2013年 | 3776篇 |
2012年 | 4972篇 |
2011年 | 5722篇 |
2010年 | 4399篇 |
2009年 | 4833篇 |
2008年 | 4084篇 |
2007年 | 5403篇 |
2006年 | 4983篇 |
2005年 | 4344篇 |
2004年 | 3486篇 |
2003年 | 3250篇 |
2002年 | 2785篇 |
2001年 | 2275篇 |
2000年 | 2003篇 |
1999年 | 1616篇 |
1998年 | 1344篇 |
1997年 | 960篇 |
1996年 | 839篇 |
1995年 | 695篇 |
1994年 | 643篇 |
1993年 | 442篇 |
1992年 | 340篇 |
1991年 | 280篇 |
1990年 | 220篇 |
1989年 | 140篇 |
1988年 | 120篇 |
1987年 | 63篇 |
1986年 | 47篇 |
1985年 | 46篇 |
1984年 | 42篇 |
1983年 | 27篇 |
1982年 | 27篇 |
1981年 | 21篇 |
1980年 | 28篇 |
1979年 | 22篇 |
1978年 | 11篇 |
1977年 | 8篇 |
1975年 | 6篇 |
1951年 | 12篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
61.
为研究古建筑木结构透榫节点的M-θ力学模型,在分析透榫节点构造特征与受力机理的基础上,建立其数值模型,用透榫节点的试验数据验证了该数值模型的正确性,并分析了节点缝隙、木材横纹弹性模量和大榫头长度对透榫节点受弯承载力的影响。根据受力分析结果,建立以弹性点、屈服点与极限点为特征点的三折线多参数M-θ力学模型,其结果与多数的试验结果基本吻合,并将该力学模型应用于木构架的受力分析。研究结果表明:透榫节点的滞回耗能能力强,节点的变形主要集中在榫头处。当榫头与卯口之间的缝隙增大时,节点的受弯承载力降低。随木材横纹弹性模量的提高和大榫头长度的增加,节点的受弯承载力有一定提高。文章建立的M-θ力学模型能较好反映透榫节点的受力过程,适用于木构架的受力分析,其荷载 位移骨架曲线与试验结果基本吻合。研究成果可为古建筑木结构的维修与保护提供参考。 相似文献
62.
以高精度三维地震资料为基础,结合构造演化恢复和区域构造背景,系统研究了准噶尔盆地车排子凸起断裂分布和形成机制。结果表明,车排子凸起发育深部和浅部2套断裂体系,深部断裂体系和浅部断裂体系分别发育3种断裂样式。车排子凸起共经历5个构造演化阶段,其中,晚二叠世挤压-逆冲控制了深部断裂体系的初始形成,晚侏罗世逆冲-走滑控制了深部断裂体系的最终定型,新近纪叠加掀斜、局部伸展控制了浅部断裂体系的形成。不同断裂体系在油气成藏过程中均起到了重要作用。其中:深部断裂体系的红车断裂是重要的油源断裂,低序级断层控制形成了石炭系火山岩优质储集体;浅部断裂体系使得油气向浅部层系运移调整,同时形成了断块圈闭、断鼻圈闭和断层-岩性圈闭等丰富的圈闭类型。 相似文献
63.
64.
《能源学会志》2020,93(6):2381-2387
To enhance the activity of catalysts for CO removal, the perovskite-type catalysts La1-xSrxCoO3 (x = 0, 0.2, 0.4, 0.6, and 0.8) with different Sr2+ doping amount were synthesized by flame spray synthesis (FSS) method. The perovskite-type catalyst synthesized by FSS has a much larger specific surface area (SSA) than that prepared by other conventional methods. The SSA of catalyst increases with the increase of Sr2+ doping amount and the SSA of La0.2Sr0.8CoO3 reaches 31.65 m2/g. Compared with other conventional methods, FSS method significantly improves the activity of catalyst and makes it close to the performances of catalysts with surface modification. The substitution of La3+ by Sr2+ promotes the generation of secondary phase Co3O4 and SrCO3. The catalytic activity of La1-xSrxCoO3 increases with the addition of Sr2+, which results from the increasing active sites and oxygen vacancies. Interestingly, La0.4Sr0.6CoO3 performs the highest activity for CO oxidation and the CO conversion reaches 50% at 148.6 °C and 90% at 165.9 °C. The oxidation of CO over La1-xSrxCoO3 catalyst may follow a combination of MvK and L-H mechanisms according to the experimental results of H2-TPR. Moreover, the catalyst exhibits good catalytic activity in consecutive oxidation cycles. In consecutive oxidation experiments with La0.4Sr0.6CoO3, the CO conversion reaches 50% at 168.8 °C and 90% at 197.8 °C in the eighth oxidation cycle. These results prove that FSS method can further improve the activity of catalysts and is suitable for the preparation of efficient catalysts. 相似文献
65.
A novel synthetic route has been proposed to prepare hausmannite nanoparticles. The synthetic route comprises an iron mediated constant current cathodic electrodeposition of manganite and heat treatment of the latter to obtain hausmannite. The obtained nanostructures have been characterized using X-ray Diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectrometry (EDX) and Fourier transform Infrared Spectrometry (FTIR). The role of iron in the formation of manganite precursor has been studied by cyclic voltammetry (CV) and differential thermal analysis (DTA). A formation mechanism based on iron mediated formation of Mn3+ and subsequent cathodic reduction of the disproportionated products has been proposed accordingly. The prepared nanoparticles exhibited specific capacitance of 143 F g−1 in 0.5 M Na2SO4 solution. The retained specific capacity was 87% after 2000 cycles. 相似文献
66.
为了寻找抗菌候选化合物,采用基于片段的药物发现方法,以氨基膦酸酯和磺酰氯为原料,设计合成了15个含膦酸酯结构单元的磺胺衍生物,经IR、1HNMR和13CNMR确认结构。采用两倍稀释法测定目标化合物的MIC(最小抑菌浓度)。结果表明:部分目标化合物呈潜在的抗菌活性,对所测试标准菌和耐药菌均有抑制活性。其中,化合物Ⅱf〔N-[(二乙氧基膦酰基)-4-氟苯甲基]-4-甲氧基苯磺酰胺〕对金黄色葡萄球菌(S. aureus)、大肠埃希菌(E. coli)、耐甲氧西林金黄色葡萄球菌(MRSA)及耐氟喹诺酮类大肠杆菌(MREC)的MIC分别为32、64、128和128μg/mL,化合物Ⅱl〔N-[(二乙氧基膦酰基)-4-氟苯甲基]-4-氟苯磺酰胺〕对S. aureus、E. coli、MRSA及MREC的MIC分别为32、32、64和64μg/mL,抗菌活性优于对照药磺胺嘧啶。 相似文献
67.
《International Journal of Hydrogen Energy》2020,45(27):13975-13984
An intervening barrier for photocatalytic water decomposition and pollutant degradation is the frustratingly quick recombination of e− - h+ pairs. Delicate design of heterojunction photocatalysts by coupling the semiconductors at nanoscale with well-matched geometrical and electronic alignments is an effective strategy to ameliorate the charge separation. Here a facile and environment-friendly l-cysteine-assisted hydrothermal process under weakly alkaline conditions is demonstrated for the first time to fabricate ZnIn2S4/In(OH)3 hollow microspheres with intimate contact, which are verified by XRD, SEM, (HR)TEM, XPS, N2 adsorption-desorption, UV–Vis DRS and photoluminescence spectra. ZnIn2S4/In(OH)3 heterostructure (L-cys/Zn2+ = 4, molar ratio) with a band-gap of 2.50 eV, demonstrates the best photocatalytic performance for water reduction and MB degradation under visible light, outperforming its counterparts (In(OH)3 and ZnIn2S4). The excellent activity of ZnIn2S4/In(OH)3 heterostructure arises from the intercrossed band-edge positions as well as the unique hollow structure with large surface area and wide pore-size distribution, which are beneficial for the efficient charge migration from bulk to surface as well as at the interface between ZnIn2S4 and In(OH)3. This work provides an efficient and eco-friendly strategy for one-pot synthesis of heterostructured composites with intimate contact for photocatalytic application. 相似文献
68.
Dr. Vlastimil Jirasko Dr. Nils-Alexander Lakomek Dr. Susanne Penzel Dr. Marie-Laure Fogeron Prof. Dr. Ralf Bartenschlager Prof. Dr. Beat H. Meier Dr. Anja Böckmann 《Chembiochem : a European journal of chemical biology》2020,21(10):1453-1460
Proton-detected 100 kHz magic-angle-spinning (MAS) solid-state NMR is an emerging analysis method for proteins with only hundreds of microgram quantities, and thus allows structural investigation of eukaryotic membrane proteins. This is the case for the cell-free synthesized hepatitis C virus (HCV) nonstructural membrane protein 4B (NS4B). We demonstrate NS4B sample optimization using fast reconstitution schemes that enable lipid-environment screening directly by NMR. 2D spectra and relaxation properties guide the choice of the best sample preparation to record 2D 1H-detected 1H,15N and 3D 1H,13C,15N correlation experiments with linewidths and sensitivity suitable to initiate sequential assignments. Amino-acid-selectively labeled NS4B can be readily obtained using cell-free synthesis, opening the door to combinatorial labeling approaches which should enable structural studies. 相似文献
69.
随着社交媒体的发展,用户之间的关系网络对于社交媒体的分析有很大的帮助。因此,该文主要研究用户好友关系检测。以往的关于用户好友关系抽取的研究主要基于社交媒体上的结构化信息,比如其他好友关系,用户的不同属性等。但是,很多时候用户本身并没有大量的好友信息存在,同时也不一定有很多确定的属性。因此,我们希望基于用户发表的文本信息来对用户关系进行预测。不同于以往的潜在好友推荐算法,该文提出了一种基于注意力机制以及长短时记忆网络(long short-term memory,LSTM)的好友关系预测模型,将好友之间的评论分开处理,通过分析用户之间的评论来判断是否具备一定的好友关系。该模型将好友双方信息拼接后的结果作为输入,并将注意力机制应用于LSTM的输出。实验表明,用户之间的评论对于好友关系预测确实有较大的实际意义,该文提出的模型较之于多个基准系统的效果,取得了明显的提升。在不加入任何其它非文本特征的情况下,实验结果的准确率达到了77%。 相似文献
70.
In this study, the decomposition of methanol into the CO and H species on the Pd/tungsten carbide (WC)(0001) surface is systematically investigated using periodic density functional theory (DFT) calculations. The possible reaction pathways and intermediates are determined. The results reveal that saturated molecules, i.e., methanol and formaldehyde, adsorb weakly on the Pd/ WC(0001) surface. Both CO and H prefer three-fold sites, with adsorption energies of −1.51 and −2.67 eV, respectively. On the other hand, CH3O stably binds at three-fold and bridge sites, with an adsorption energy of −2.58 eV. However, most of the other intermediates tend to adsorb to the surface with the carbon and oxygen atoms in their sp3 and hydroxyl-like configurations, respectively. Hence, the C atom of CH2OH preferentially attaches to the top sites, CHOH and CH2O adsorb at the bridge sites, while COH and CHO occupy the three-fold sites. The DFT calculations indicate that the rupture of the initial C–H bond promotes the decomposition of CH3OH and CH2OH, whereas in the case of CHOH, O–H bond scission is favored over the C–H bond rupture. Thus, the most probable methanol decomposition pathway on the Pd/WC(0001) surface is CH3OH → CH2OH → trans-CHOH → CHO → CO. The present study demonstrates that the synergistic effect of WC (as carrier) and Pd (as catalyst) alters the CH3OH decomposition pathway and reduces the noble metal utilization. 相似文献