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51.
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研究了不同工艺参数对980 MPa级连续退火双相钢组织及力学性能的影响,利用光学显微镜、透射电镜(TEM)以及拉伸试验对双相钢的微观组织和力学性能进行测试及分析。结果表明:DP980钢的退火组织主要由铁素体、马氏体岛和少量的贝氏体组成,马氏体岛附近的位错密度较高。随着均热温度的升高,DP980钢的抗拉强度呈现先降低后升高的趋势,屈服强度与抗拉强度的趋势一致,伸长率先升高后降低。随着过时效温度的升高,DP980钢的抗拉强度和屈服强度降低,降低幅度较小,伸长率上升,但变化不明显,说明通过调整过时效温度来调控其力学性能的作用较小。 相似文献
53.
Polymer Bulletin - Preparation of konjac glucomannan-grafted poly(trimethyl allyl ammonium chloride) (KGM-g-PTMAAC) was carried out using KGM as polysaccharide matrix and TMAAC as cationic... 相似文献
54.
Zhongkai Zhao Yohanes A. Situmorang Ping An Nichaboon Chaihad Jing Wang Xiaogang Hao Guangwen Xu Abuliti Abudula Guoqing Guan 《化学工程与技术》2020,43(4):625-640
In the future, hydrogen will be an important energy carrier and industrial raw material. Catalytic steam reforming of bio-oils is a promising and economically viable technology for hydrogen production. However, during the reforming process, the catalysts are rapidly deactivated due to coke formation and sintering. Thus, maintaining the activity and stability of catalysts is the key issue in this process. Optimized operation conditions could extend the catalyst lifetime by affecting the coke morphology or promoting coke gasification. This article summarizes the recent developments in the field of catalytic steam reforming of bio-oils, focusing on the operation conditions, the properties of the catalysts, and the effects of the catalyst supports. The expected insights into the catalytic steam reforming of bio-oils will provide further guidance for hydrogen production from bio-oils. 相似文献
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济阳坳陷下古生界潜山油气藏特征及成藏模式 总被引:1,自引:1,他引:0
济阳坳陷下古生界潜山具有多样性、复杂性的特点,潜山差异性的形成演化、油气成藏主控因素和控藏模式不明确,严重制约了该区潜山油气勘探。在潜山分类的基础上,综合利用系统恢复、分类对比和典型解剖等方法,揭示了济阳坳陷下古生界不同类型潜山的形成演化过程和油气成藏主控因素差异性,分类建立了油气成藏模式。研究表明,济阳坳陷下古生界主要发育高位新盖侵蚀残丘潜山、中位古盖拉张断块潜山、中位新古盖拉张剪切断块潜山、中位中古盖挤压拉张断块潜山和低位古盖拉张滑脱断块潜山5种潜山类型。不同类型潜山的形成演化和油气成藏各具特色,其中,高位新盖侵蚀残丘潜山的发育受隆升、侵蚀作用控制,油气成藏主要受控于油源和盖层条件,表现为"单向供烃、砂体-不整合岩溶体联合输导、残丘控藏"的成藏模式;中位古盖拉张断块潜山的发育受掀斜、断裂作用控制,油气成藏主要受控于储集条件,表现为"单向供烃、顺向断层输导、反向断层控藏"的成藏模式;中位新古盖拉张剪切断块潜山的发育受反转、翘倾和走滑切割作用控制,油气成藏主要受控于输导条件,表现为"多源供烃、断溶体立体输导、断裂控藏"的成藏模式;中位中古盖挤压拉张断块潜山的形成受强烈挤压、拉张滑脱作用控制,油气成藏主要受控于储集条件,表现为"多源供烃、断缝体输导、断褶控藏"的成藏模式;低位古盖拉张滑脱断块潜山的形成受强烈拉张滑脱作用控制,油气成藏主要受控于输导条件,表现为"顶部供烃、断缝体输导、断裂控藏"的成藏模式。 相似文献
58.
Wang Yi-Ting Shen Jie Li Zhi-Xu Yang Qiang Liu An Zhao Peng-Peng Xu Jia-Jie Zhao Lei Yang Xun-Jie 《计算机科学技术学报》2020,35(4):724-738
Journal of Computer Science and Technology - Entity linking (EL) is the task of determining the identity of textual entity mentions given a predefined knowledge base (KB). Plenty of existing... 相似文献
59.
Ning An Yunhao Cai Hongbo Wu Ailing Tang Kangning Zhang Xiaotao Hao Zaifei Ma Qiang Guo Hwa Sook Ryu Han Young Woo Yanming Sun Erjun Zhou 《Advanced materials (Deerfield Beach, Fla.)》2020,32(39):2002122
Compared with inorganic or perovskite solar cells, the relatively large non-radiative recombination voltage losses (ΔVnon-rad) in organic solar cells (OSCs) limit the improvement of the open-circuit voltage (Voc). Herein, OSCs are fabricated by adopting two pairs of D–π–A polymers (PBT1-C/PBT1-C-2Cl and PBDB-T/PBDB-T-2Cl) as electron donors and a wide-bandgap molecule BTA3 as the electron acceptor. In these blends, a charge-transfer state energy (ECT) as high as 1.70–1.76 eV is achieved, leading to small energetic differences between the singlet excited states and charge-transfer states (ΔECT ≈ 0.1 eV). In addition, after introducing chlorine atoms into the π-bridge or the side chain of benzodithiophene (BDT) unit, electroluminescence external quantum efficiencies as high as 1.9 × 10−3 and 1.0 × 10−3 are realized in OSCs based on PBTI-C-2Cl and PBDB-T-2Cl, respectively. Their corresponding ΔVnon-rad are 0.16 and 0.17 V, which are lower than those of OSCs based on the analog polymers without a chlorine atom (0.21 and 0.24 V for PBT1-C and PBDB-T, respectively), resulting in high Voc of 1.3 V. The ΔVnon-rad of 0.16 V and Voc of 1.3 V achieved in PBT1-C-2Cl:BTA3 OSCs are thought to represent the best values for solution-processed OSCs reported in the literature so far. 相似文献
60.
Bo Wang Edison Huixiang Ang Yang Yang Yufei Zhang Hongbo Geng Minghui Ye Cheng Chao Li 《Advanced functional materials》2020,30(28)
Orthorhombic molybdenum trioxide (MoO3) is one of the most promising anode materials for sodium‐ion batteries because of its rich chemistry associated with multiple valence states and intriguing layered structure. However, MoO3 still suffers from the low rate capability and poor cycle induced by pulverization during de/sodiation. An ingenious two‐step synthesis strategy to fine tune the layer structure of MoO3 targeting stable and fast sodium ionic diffusion channels is reported here. By integrating partially reduction and organic molecule intercalation methodologies, the interlayer spacing of MoO3 is remarkably enlarged to 10.40 Å and the layer structural integration are reinforced by dimercapto groups of bismuththiol molecules. Comprehensive characterizations and density functional theory calculations prove that the intercalated bismuththiol (DMcT) molecules substantially enhanced electronic conductivity and effectively shield the electrostatic interaction between Na+ and the MoO3 host by conjugated double bond, resulting in improved Na+ insertion/extraction kinetics. Benefiting from these features, the newly devised layered MoO3 electrode achieves excellent long‐term cycling stability and outstanding rate performance. These achievements are of vital significance for the preparation of sodium‐ion battery anode materials with high‐rate capability and long cycling life using intercalation chemistry. 相似文献