首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   3559篇
  免费   226篇
  国内免费   19篇
电工技术   42篇
综合类   8篇
化学工业   619篇
金属工艺   47篇
机械仪表   96篇
建筑科学   102篇
矿业工程   1篇
能源动力   137篇
轻工业   215篇
水利工程   15篇
石油天然气   7篇
无线电   570篇
一般工业技术   593篇
冶金工业   755篇
原子能技术   9篇
自动化技术   588篇
  2023年   19篇
  2022年   56篇
  2021年   88篇
  2020年   58篇
  2019年   72篇
  2018年   90篇
  2017年   87篇
  2016年   102篇
  2015年   93篇
  2014年   141篇
  2013年   281篇
  2012年   197篇
  2011年   185篇
  2010年   176篇
  2009年   178篇
  2008年   167篇
  2007年   151篇
  2006年   120篇
  2005年   94篇
  2004年   76篇
  2003年   82篇
  2002年   78篇
  2001年   59篇
  2000年   56篇
  1999年   83篇
  1998年   261篇
  1997年   148篇
  1996年   109篇
  1995年   81篇
  1994年   61篇
  1993年   55篇
  1992年   28篇
  1991年   32篇
  1990年   35篇
  1989年   35篇
  1988年   24篇
  1987年   17篇
  1986年   16篇
  1985年   22篇
  1984年   11篇
  1983年   14篇
  1982年   8篇
  1981年   7篇
  1980年   8篇
  1979年   3篇
  1978年   3篇
  1977年   9篇
  1976年   16篇
  1974年   2篇
  1970年   4篇
排序方式: 共有3804条查询结果,搜索用时 10 毫秒
141.
Ha H  Payer J 《Electrochimica acta》2011,(7):2781-2791
The precipitation and growth of AgCl on silver in physiological NaCl solution were investigated. AgCl was found to form at bottom of scratches on the surface which may be the less effective sites for diffusion or the favorable sites for heterogeneous nucleation. Patches of silver chloride expanded laterally on the substrate until a continuous film formed. The ionic transport path through this newly formed continuous film was via spaces between AgCl patches. As the film grew, the spaces between AgCl patches closed and ion transport was primarily via micro-channels running through AgCl patches. The decrease of AgCl layer conductivity during film growth were attributed to the clogging of micro-channels or decrease in charge carrier concentration inside the micro-channels. Under thin AgCl layer, i.e. on the order of a micrometer, the dissolution of silver substrate was under mixed activation-Ohmic control. Under thick AgCl layer, i.e. on the order of tens of micrometers, the dissolution of silver substrate was mediated by the Ohmic resistance of AgCl layer.  相似文献   
142.
The pit propagation behavior of copper (UNS C11000) was investigated from an electrochemical perspective using the artificial pit method. Pit growth was studied systematically in a range of HCO3, SO42− and Cl containing-waters at various concentrations. Pit propagation was mediated by the nature of the corrosion products formed both inside and over the pit mouth (i.e., cap). Certain water chemistry concentrations such as those high in sulfate were found to promote fast pitting that could be sustained over long times at a fixed applied potential but gradually stifled in all but the lowest concentration solutions. In contrast, Cl containing waters without sulfate ions resulted in slower pit growth and eventual repassivation. These observations were interpreted through understanding of the identity, amount and porosity of corrosion products formed inside and over pits. These factors controlled their resistive nature as characterized using electrochemical impedance spectroscopy. A finite element model (FEM) was developed which included copper oxidation kinetics, transport by migration and diffusion, Cu(I) and Cu(II) solid corrosion product formation and porosity governed by equilibrium thermodynamics and a saturation index, as well as pit current and depth of penetration. The findings of the modeling were in good agreement with artificial pit experiments. Malachite, bronchantite, cuprite, nantokite and atacamite corrosion products were both observed in experiment and predicted by the model. Stifling and/or repassivation occurred when the resistance of the corrosion product layer became high enough to lower the pit bottom potential and pit current density such as 10-5 A/cm2 could be attained with thick and dense layer. The ramifications of these findings towards pit propagation characteristics in potable waters will be discussed with improved insight into the roles of Cl and SO42− ions.  相似文献   
143.
The Mode I interlaminar fracture behavior of woven carbon fiber/epoxy composite laminates incorporating partially cured carbon nanotube/epoxy composite films has been investigated. Laminates with films containing carbon nanotubes (CNTs) in the as‐received state and functionalized with polyamidoamine were evaluated, as well as laminates with neat epoxy films. Double‐cantilever beam (DCB) specimens were used to measure GIc, the critical strain energy release rate (fracture toughness) versus crack length. Post‐fracture microscopic inspection of the fracture surfaces was performed. Results show that initial fracture toughness was improved with the amino‐functionalized CNT/epoxy interleaf films, but the important factor appears to be the polyamidoamine functionalization, not the CNTs. The initial fracture toughness remained relatively unaffected with the incorporation of neat epoxy and as‐received CNT/epoxy interleaf films. Plateau fracture toughness was unchanged with the use of functionalized CNT/epoxy interleaf films, and was reduced with the use of neat epoxy and as‐received CNT/epoxy interleaf films. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011  相似文献   
144.
M.L. DigarS.L. Hung  T.C. Wen 《Polymer》2002,43(5):1615-1622
A series of cross-linked polyurethane acrylate (PUA) electrolytes have been prepared by using 4,4′-methylene bis(phenyl isocyanate), polyethylene glycol, hydroxyethyl methacrylate and different reactive vinyl/divinyl diluents, such as methyl methacrylate (MMA), ethyl acrylate and acrylonitrile, tripropylene glycol diacrylate (TPGDA). The electrolytes were prepared by UV radiation induced cross-linking of the PUA-diluent mixture followed by swelling in a liquid electrolyte (LP-30). Depending upon the composition of the components, these electrolytes exhibited a wide range of mechanical and electrical properties. The system containing MMA as reactive diluent showed highest conductivity, but poor mechanical properties and stability in the liquid electrolyte. The TPGDA cross-linked system possesses a good combination of ionic conductivity and stability in liquid electrolytes. These systems showed good compatibility with Li-electrodes and sufficient electrochemical stability to allow safe operation in rechargeable Li-batteries.  相似文献   
145.
The equilibrium and kinetics of solvent extraction of Cu2+ from aqueous solutions containing equimolar EDTA with Aliquat 336 in n‐decanol and kerosene at 298 K were investigated. The concentrations of Cu2+ (8–50 mol m?3), Cl? (5–60 mol m?3), and Aliquat 336 (20–100 mol m?3) were varied. A semi‐empirical model with three parameters was proposed to describe the equilibrium behavior, in which the non‐idealities in both aqueous and organic phases were considered. Over the ranges studied, the model agreed reasonably well with the experimental data (standard deviation, 15%). The forward and backward reaction rate constants were determined as (5.31 ± 0.16)×10?6 m9/4 mol?3/4 s?1 and (2.62 ± 0.09)×10?7 s?1, respectively, at 298 K. An interfacial reaction mechanism was proposed, which revealed that the reaction between the chelated anions and trimeric amine molecules at the interface was rate limiting. The derived rate laws were consistent with the experimental results. © 2002 Society of Chemical Industry  相似文献   
146.
A new diimide–diacid monomer, N,N′‐bis(4‐carboxyphenyl)‐4,4′‐oxydiphthalimide (I), was prepared by azeotropic condensation of 4,4′‐oxydiphthalic anhydride (ODPA) and p‐aminobenzoic acid (p‐ABA) at a 1:2 molar ratio in a polar solvent mixed with toluene. A series of poly(amide–imide)s (PAI, IIIa–m) was synthesized from the diimide–diacid I (or I′, diacid chloride of I) and various aromatic diamines by direct polycondensation (or low temperature polycondensation) using triphenyl phosphite and pyridine as condensing agents. It was found that only IIIk–m having a meta‐structure at two terminals of the diamine could afford good quality, creasable films by solution‐casting; other PAIs III using diamine with para‐linkage at terminals were insoluble and crystalline; though IIIg–i contained the soluble group of the diamine moieties, their solvent‐cast films were brittle. In order to improve their to solubility and film quality, copoly(amide–imide)s (Co‐PAIs) based on I and mixtures of p‐ABA and aromatic diamines were synthesized. When on equimolar of p‐ABA (m = 1) was mixed, most of Co‐PAIs IV had improved solubility and high inherent viscosities in the range 0.9–1.5 dl g?1; however, their films were still brittle. With m = 3, series V was obtained, and all members exhibited high toughness. The solubility, film‐forming ability, crystallinity, and thermal properties of the resultant poly(amide–imide)s were investigated. © 2002 Society of Chemical Industry  相似文献   
147.
A quick method of preparing transparent organic-inorganic hybrid material was studied. The hybrid, PVA/PSA, was prepared through incorporating the nanoscaled polysilicic acid (PSA) obtained through hydrolysis and condensation of metasilicate salt directly into a polyvinyl alcohol (PVA). The interfacial force, microstructure, and dynamic mechanical property of the hybrid were studied by means of spectroscopy (FTIR, X-ray diffraction and solid-state 29Si NMR) and dynamic mechanical analysis, and the results were compared with that of the hybrids, PVA/TEOS, prepared through the traditional sol-gel process. It was found that the microstructure of PVA/PSA was different from that of PVA/TEOS because of the different preparation methods. The structures of the crystals in both hybrids were similar to that of the pure PVA. Other physical properties, such as Tg, storage modulus, tensile strength and solvent resistance of the PVA/PSA hybrid, were improved significantly with the addition of the silica content. The extent of improvement was a little lower than that for the PVA/TEOS.  相似文献   
148.
Due to the high cost of adsorbents and their thermal regeneration in recent years,much research has focused on the search for cheaper adsorbents for treating wastewater from textile industry.The single component adsorption of an acidic dye,Acid Yellow 117,and a basic dye,Methylene Blue,onto several adsorbents—bamboo,waste wood,bamboo char,waste wood char,bamboo activated carbon,wood activated carbon and active carbon F400 were conducted.Based on a Langmuir analysis,the monolayer adsorption capacities were determined.Three of the adsorbents were selected for binary layer adsorption to check the multilayer concept and the potential application for better adsorbent usage.The two cheapest adsorbents,bamboo and wood are compared with the commercial activated carbon F400,and all three systems were successful.  相似文献   
149.
From a high-throughput screening (HTS) hit with inhibitory activity against virus-induced cytophathic in the low micromolar range, we have developed a potent anti-influenza lead through careful optimization without compromising the drug-like properties of the compound. An orally bioavailable compound was identified as a lead agent with nanomolar activity against influenza, representing a 140-fold improvement over the initial hit.  相似文献   
150.
Psychophysical experiments were conducted in the UK, Taiwan, France, Germany, Spain, Sweden, Argentina, and Iran to assess colour emotion for two‐colour combinations using semantic scales warm/cool, heavy/light, active/passive, and like/dislike. A total of 223 observers participated, each presented with 190 colour pairs as the stimuli, shown individually on a cathode ray tube display. The results show consistent responses across cultures only for warm/cool, heavy/light, and active/passive. The like/dislike scale, however, showed some differences between the observer groups, in particular between the Argentinian responses and those obtained from the other observers. Factor analysis reveals that the Argentinian observers preferred passive colour pairs to active ones more than the other observers. In addition to the cultural difference in like/dislike, the experimental results show some effects of gender, professional background (design vs. nondesign), and age. Female observers were found to prefer colour pairs with high‐lightness or low‐chroma values more than their male counterparts. Observers with a design background liked low‐chroma colour pairs or those containing colours of similar hue more than nondesign observers. Older observers liked colour pairs with high‐lightness or high‐chroma values more than young observers did. Based on the findings, a two‐level theory of colour emotion is proposed, in which warm/cool, heavy/light, and active/passive are identified as the reactive‐level responses and like/dislike the reflective‐level response. © 2010 Wiley Periodicals, Inc. Col Res Appl, 2012  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号