全文获取类型
收费全文 | 92325篇 |
免费 | 1686篇 |
国内免费 | 490篇 |
专业分类
电工技术 | 945篇 |
综合类 | 2360篇 |
化学工业 | 13878篇 |
金属工艺 | 4958篇 |
机械仪表 | 3381篇 |
建筑科学 | 2484篇 |
矿业工程 | 578篇 |
能源动力 | 1727篇 |
轻工业 | 4491篇 |
水利工程 | 1415篇 |
石油天然气 | 483篇 |
武器工业 | 5篇 |
无线电 | 10091篇 |
一般工业技术 | 17737篇 |
冶金工业 | 2802篇 |
原子能技术 | 314篇 |
自动化技术 | 26852篇 |
出版年
2024年 | 43篇 |
2023年 | 198篇 |
2022年 | 372篇 |
2021年 | 641篇 |
2020年 | 578篇 |
2019年 | 713篇 |
2018年 | 15018篇 |
2017年 | 13897篇 |
2016年 | 10532篇 |
2015年 | 1030篇 |
2014年 | 944篇 |
2013年 | 1248篇 |
2012年 | 3755篇 |
2011年 | 10040篇 |
2010年 | 8670篇 |
2009年 | 5921篇 |
2008年 | 6977篇 |
2007年 | 7920篇 |
2006年 | 256篇 |
2005年 | 1300篇 |
2004年 | 1219篇 |
2003年 | 1221篇 |
2002年 | 587篇 |
2001年 | 121篇 |
2000年 | 196篇 |
1999年 | 79篇 |
1998年 | 71篇 |
1997年 | 44篇 |
1996年 | 66篇 |
1995年 | 28篇 |
1994年 | 21篇 |
1993年 | 23篇 |
1992年 | 21篇 |
1991年 | 39篇 |
1988年 | 16篇 |
1969年 | 24篇 |
1968年 | 43篇 |
1967年 | 34篇 |
1966年 | 42篇 |
1965年 | 44篇 |
1963年 | 28篇 |
1962年 | 22篇 |
1961年 | 18篇 |
1960年 | 30篇 |
1959年 | 35篇 |
1958年 | 37篇 |
1957年 | 36篇 |
1956年 | 34篇 |
1955年 | 63篇 |
1954年 | 68篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
71.
Influence of pencil lead hardness on voltammetric response of graphite reinforcement carbon electrodes 总被引:1,自引:0,他引:1
Paulo Henrique Campos Prado Tavares Paulo Jorge Sanches Barbeira 《Journal of Applied Electrochemistry》2008,38(6):827-832
This work studied the voltammetric response of graphite reinforcement electrodes made of different pencil lead hardness. The
studies showed that harder graphite leads, regardless of their manufacturer, are more appropriate as electrode material for
voltammetric purposes due to their higher peak currents, increasing sensitivity and reproducibility, with ΔEp closer to the theoretical value for a reversible system. 相似文献
72.
In the present work, the ohmic resistance of an integrated planar-SOFC (IP-SOFC) has been evaluated by developing a model
whose equations have been solved numerically through an FEM method. The model allows to estimate the distribution of voltage
and current density in the cell. A comparison between simulated and experimental data of area specific resistance is reported,
which shows satisfactory agreement. The mathematical model has also been used to carry out some parametric studies for optimisation
purposes. Indeed, a reduction in cell pitch length and an increase in electrode thickness are predicted to lead to a reduction
in ohmic losses in IP-SOFCs. 相似文献
73.
Polymer/Silica nanocomposite latex particles were prepared by emulsion polymerization of methyl methacrylate (MMA) with dimethylaminoethyl methacrylate (DM). The reaction was performed using a nonionic surfactant and in the presence of silica nanoparticles as the seed. The polymer‐coated silica nanoparticles with polymer content and number average particle sizes ranged from 32 to 93 wt % and 114–310 nm, respectively, were obtained depending on reaction conditions. Influences of some synthetic conditions such as MMA, DM, surfactant concentration, and the nature of initiator on the coating of the silica nanoparticles were studied. Electrostatic attraction between anionic surface of silica beads and cationic amino groups of DM is the main driving force for the formation of the nanocomposites. It was demonstrated that the ratio of DM/MMA is important factor in stability of the system. The particle size, polymer content, efficiency of the coating reaction, and morphology of resulted nanocomposite particles showed a dependence on the amount of the surfactant. Zeta potential measurements confirmed that the DM was located at the surface of the nanocomposites particles. Thermogravimeteric analysis indicated a relationship between the composition of polymer shell and polymer content of the nanocomposites. The nanocomposites were also characterized by FTIR and differential scanning calorimetry techniques. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献
74.
Reda Karoum Antonio de Lucas-Consuegra Fernando Dorado Jose Luis Valverde Alain Billard Philippe Vernoux 《Journal of Applied Electrochemistry》2008,38(8):1083-1088
The electrochemical promotion of catalysis (EPOC) of propene combustion was investigated using Pt sputtered thin film on an
O2− conductor, 8 mol% Y2O3-stabilized-ZrO2 (YSZ). In order to separate the influence of the thermal migration of the O2− oxide ions from the electrolyte to the catalyst surface and the impact of an electrical polarization on the catalytic activity,
several light-off experiments (cool down and heat up procedures) were successively performed under different polarizations,
i.e. OCV, +2 and −2 V. These experiments have clearly shown that the presence of O2− (thermally or electrochemically induced) inhibits the catalytic activity of the platinum for the propene deep oxidation.
These results demonstrate the importance to define a normalized rate enhancement ratio, ρ
n
, from a reference value of the catalytic rate corresponding to a Pt surface state free of O2− ions. 相似文献
75.
Habibeh Haddad Dabaghi Abdolmajid Bayandori Moghaddam Mahmood Kazemzad Rassoul Dinarvand Fezze Aryanasab Mohammad Reza Nabid 《Journal of Applied Electrochemistry》2008,38(3):409-413
Electrochemical treatment processes can significantly contribute to the protection of the environment through the minimization
of waste and toxic materials in effluents. From a pharmaceutical point of view and due to the existing resemblance between
the electrochemical and biological reactions, it can be assumed that the oxidation mechanisms on the electrode and in the
body share similar principles. In this paper, the application of electrochemical studies in the design of an environmentally
friendly method was delineated for the new hydrocaffeic acid (HCA, 3,4-dihydroxy hydrocinnamic acid) derivatives synthesis
at carbon electrodes in an undivided cell. In this cell, the EC mechanism reaction was involved, comprising two steps alternatively;
(1) electrochemical oxidation and (2) chemical reaction. In particular, the electro-organic reactions of HCA, an important
biological molecule, were studied in a water–acetonitrile (90:10 v/v) mixture in the presence of benzenesulfinic acid (3) and p-toluenesulfinic acid (4). The research included the use of a variety of experimental techniques, such as cyclic voltammetry, controlled-potential
electrolysis and product spectroscopic identification. 相似文献
76.
Namsin Park Takeyuki Shiraishi Kazuyoshi Kamisugi Yoshitaka Hara Keita Iizuka Takashi Kado Shuzi Hayase 《Journal of Applied Electrochemistry》2008,38(3):371-375
A direct ethanol fuel cell (DEFC), which is less prone to ethanol crossover, is reported. The cell consists of PtRu/C catalyst as the anode, Nafion® 117 membrane, and Ni–Co–Fe (NCF) composite catalyst as the cathode. The NCF catalyst was synthesized by mixing Ni, Co, and Fe complexes into a polymer matrix (melamine-formaldehyde resins), followed by heating the mixture at 800 °C under inert atmosphere. TEM and EDX experiments suggest that the NCF catalyst has alloy structures of Ni, Co and Fe. The catalytic activity of the NCF catalyst for the oxygen reduction reaction (ORR) was compared with that of commercially available Pt/C (CAP) catalyst at different ethanol concentrations. The decrease in open circuit voltage (Voc) of the DEFC equipped with the NCF catalysts was less than that of CAP catalyst at higher ethanol concentrations. The NCF catalyst was less prone to ethanol oxidation at cathode even when ethanol crossover occurred through the Nafion®117 film, which prevents voltage drop at the cathode. However, the CAP catalyst did oxidize ethanol at the cathode and caused a decrease in voltage at higher ethanol concentrations. 相似文献
77.
Khalid Mahmood Zia Mehdi Barikani Ijaz Ahmad Bhatti Mohammad Zuber Haq Nawaz Bhatti 《应用聚合物科学杂志》2008,109(3):1840-1849
A series of polyurethane (PU) elastomers was prepared by the reaction of poly(?‐caprolactone) and 4,4′‐diphenylmethane diisocyanate, which was extended with a series of chain extenders (CEs) having 2–10 methylene units in their structure. The completion of the reaction was confirmed by Fourier transform infrared spectroscopy. The chemical structures of the synthesized PU samples were characterized with Fourier transform infrared, 1H‐NMR, and 13C‐NMR spectroscopy, and the thermal properties were determined by thermogravimetric analysis, DSC, and dynamic mechanical thermal analysis techniques. The mechanical properties were also studied and are discussed. The thermogravimetric analysis and DSC analysis showed that CE length had a considerable effect on the thermal properties of the prepared samples. The dynamic mechanical thermal analysis and damping peaks were also affected by the number of methylene units in the CE length. The elastomer extended with 1,2‐ethane diol exhibited optimum thermal properties, whereas the elastomer based on 1,10‐decane diol displayed the worst thermal properties. Tensile strength and elongation at break decreased with increasing CE length, whereas hardness showed the opposite trend. The glass‐transition temperature moved toward lower temperatures with increasing CE length. The decrease in the glass‐transition temperature and tensile properties were interpreted in terms of decreasing hard segments and increasing chain flexibility. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献
78.
79.
80.
Johan F. Hoorn 《Cognition, Technology & Work》2008,10(4):249-249