全文获取类型
收费全文 | 125866篇 |
免费 | 20986篇 |
国内免费 | 4192篇 |
专业分类
电工技术 | 5742篇 |
技术理论 | 7篇 |
综合类 | 6470篇 |
化学工业 | 31248篇 |
金属工艺 | 5921篇 |
机械仪表 | 6340篇 |
建筑科学 | 8683篇 |
矿业工程 | 3033篇 |
能源动力 | 3556篇 |
轻工业 | 12186篇 |
水利工程 | 1933篇 |
石油天然气 | 5961篇 |
武器工业 | 737篇 |
无线电 | 16115篇 |
一般工业技术 | 21180篇 |
冶金工业 | 5118篇 |
原子能技术 | 957篇 |
自动化技术 | 15857篇 |
出版年
2024年 | 360篇 |
2023年 | 1379篇 |
2022年 | 2329篇 |
2021年 | 3566篇 |
2020年 | 3869篇 |
2019年 | 5257篇 |
2018年 | 5473篇 |
2017年 | 6035篇 |
2016年 | 6173篇 |
2015年 | 7169篇 |
2014年 | 7898篇 |
2013年 | 9692篇 |
2012年 | 7864篇 |
2011年 | 7985篇 |
2010年 | 7802篇 |
2009年 | 7392篇 |
2008年 | 6796篇 |
2007年 | 6570篇 |
2006年 | 6500篇 |
2005年 | 5499篇 |
2004年 | 4455篇 |
2003年 | 4716篇 |
2002年 | 5322篇 |
2001年 | 4528篇 |
2000年 | 3475篇 |
1999年 | 2946篇 |
1998年 | 1837篇 |
1997年 | 1535篇 |
1996年 | 1552篇 |
1995年 | 1233篇 |
1994年 | 926篇 |
1993年 | 716篇 |
1992年 | 549篇 |
1991年 | 395篇 |
1990年 | 307篇 |
1989年 | 246篇 |
1988年 | 215篇 |
1987年 | 129篇 |
1986年 | 89篇 |
1985年 | 60篇 |
1984年 | 53篇 |
1983年 | 40篇 |
1982年 | 37篇 |
1981年 | 21篇 |
1980年 | 33篇 |
1979年 | 8篇 |
1978年 | 4篇 |
1977年 | 3篇 |
1951年 | 4篇 |
1890年 | 1篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
991.
以钠硼解石天然矿粉为原料,经水热解聚和相转化制备出硼酸钙产品。通过化学分析、XRD及TG—DTG分析表明:产品中的物相主要是白硼钙石(4CaO·5B2O3-7H2O)、硬硼钙石(2CaO·3B2O3·5H2O)和羟硼钙石(3CaO·2B2O3·9H2O)。实验确定了适宜的工艺条件,即:反应体系液固体积质量比为2.5mL/g左右;解聚温度120℃;解聚时间8h左右;干燥温度在200℃左右。在此工艺条件下制得的硼酸钙产品的氧化钠质量分数在0.5%以下,很好地满足了无碱玻璃纤维工业对含硼原料的要求。 相似文献
992.
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
993.
Hydrophilic coatings based on 3‐glicidoxy propyl trimethoxy silane (GPTMS) and polyethylene glycol (PEG) were prepared with the incorporation of tetramethoxysilane (TMOS) and silica nanoparticle colloidal suspension by a sol–gel process. Characterization of the coatings has been performed by Fourier Transform Infrared (FTIR) and Attenuated Total Reflectance Infrared (ATR‐IR) techniques. Morphological properties were characterized by Scanning Electron Microscopy (SEM). The distribution of Si atoms in the hybrid system was obtained by Si mapping. The particle size in sol solution of the coating was measured by light scattering analyzer. Optical properties were characterized by using UV–vis spectrophotometer. The hydrophilicity of the coating was determined by contact angle measurements, and also the results have been confirmed by surface energy and water uptake investigations. The obtained results indicate that the surfactants affected the contact angles remarkably but did not change the transparency. It has been found that applying silica nano particles leads to coatings with different properties than those using TMOS, while siloxane contents were the same in these two set of coatings. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 5322–5329, 2006 相似文献
994.
The reactive compatibilization of syndiotactic polystyrene (sPS)/oxazoline‐styrene copolymer (RPS)/maleic anhydride grafted ethylene‐propylene copolymer (EPR‐MA) blends is investigated in this study. First, the miscibility of sPS/RPS blends is examined by thermal analysis. The cold crystallization peak (Tcc) moved toward higher temperature with increased PRS, and, concerning enthalpy relaxation behaviors, only a single enthalpy relation peak was found in all aged samples. These results indicate that the sPS/RPS blend is miscible along the various compositions and RPS can be used in the reactive compatibilization of sPS/RPS/EPR‐MA blends. The reactive compatibilized sPS/RPS/EPR‐MA blends showed finer morphology than sPS/EPR‐MA physical blends and higher storage modulus (G') and complex viscosity (η*) when RPS contents were increased. Moreover, the impact strength of sPS/RPS/EPR‐MA increased significantly compared to sPS/EPR‐MA blend, and SEM micrographs after impact testing show that the sPS/RPS/EPR‐MA blend has better adhesion between the sPS matrix and the dispersed EPR‐MA phase. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 2084–2091, 2002 相似文献
995.
Neung‐Ju Lee Ja‐Chul Koo Sung‐Suk Ju Seong‐Bae Moon Won‐Jei Cho In‐Cheol Jeong Song‐Jae Lee Moo‐Youn Cho Emmanuel A Theodorakis 《Polymer International》2002,51(7):569-576
The attachment of anticancer agents to polymers is a promising approach towards reducing the toxic side‐effects and retaining the potent antitumour activity of these agents. A new tetrahydrophthalimido monomer containing 5‐fluorouracil (ETPFU) and its homopolymer and copolymers with acrylic acid (AA) and with vinyl acetate (VAc) have been synthesized and spectroscopically characterized. The ETPFU contents in poly(ETPFU‐co‐AA) and poly(ETPFU‐co‐VAc) obtained by elemental analysis were 21 mol% and 20 mol%, respectively. The average molecular weights of the polymers determined by gel permeation chromatography were as follows: Mn = 8900 g mol?1, Mw = 13 300 g mol?1, Mw/Mn = 1.5 for poly(ETPFU); Mn = 13 500 g mol?1, Mw = 16 600 g mol?1, Mw/Mn = 1.2 for poly(ETPFU‐co‐AA); Mn = 8300 g mol?1, Mw = 11 600 g mol?1, Mw/Mn = 1.4 poly(ETPFU‐co‐VAc). The in vitro cytotoxicity of the compounds against FM3A and U937 cancer cell lines increased in the following order: ETPFU > 5‐FU > poly(ETPFU) > poly(ETPFU‐co‐AA) > poly(ETPFU‐co‐VAc). The in vivo antitumour activities of all the polymers in Balb/C mice bearing the sarcoma 180 tumour cell line were greater than those of 5‐FU and monomer at the highest dose (800 mg kg?1). © 2002 Society of Chemical Industry 相似文献
996.
M. S. Hedenqvist J. E. Ritums M. Cond‐Brana G. Bergman 《Polymer Engineering and Science》2004,44(1):113-122
The transport of water, hydrochloric acid, hydrobromic acid and tetrachloroethylene in an poly(ethylene‐co‐chlorotrifluoroethylene) and polyvinylidene fluoride were studied at 70°C by the sorption/desorption technique. The effects on the structure and mechanical properties were studied using size‐exclusion chromatography, infrared spectroscopy, differential scanning calorimetry and tensile testing. Solute concentrations in the polymers indicated that both the water and HCl/HBr components diffused into the polymers on exposure to acid solutions. The calculated water contents of the diffusing acids generally differed from the water content in the solution. The ratio of water content in the diffusing acid to that in the surrounding acid solution was generally a function of the relative vapor activity of water and HCl/HBr. It was possible to describe the 35%HCl and 47%HBr desorption data using a two component model. It was here assumed that the water and HCl/HBr diffused separately, each having its own constant diffusion coefficient. The water diffusivity was obtained from the pure water system, and this allowed the HCl/HBr diffusivity to be calculated. It was found that the diffusivity decreased, in a non‐simple way, as a function of solute size. The exposure to solute did not lower the molar mass of the polyvinylidene fluoride. Differential scanning calorimetry indicated the development of low‐melting point polyvinylidene fluoride crystals during the exposure to all solutes. This seemed to be a consequence of the long‐term exposure (175 to 376 days) at 70°C. The long‐term exposure stiffened several of the polyvinylidene fluoride resins and occasionally made them less ductile. The poly(ethylene‐co‐chlorotrifluoroethylene) also became stiffer, but it was otherwise unaffected as far as observation by the other available techniques was concerned. 相似文献
997.
Jan‐Chan Huang 《应用聚合物科学杂志》2004,91(5):2894-2902
Experimental values of the Flory–Huggins parameter, χ, between polymers and solvents, are frequently used to determine the solubility parameters of the polymers. A method using nonlinear curve fitting of RTχ/V was compared to the linear regression method commonly used. It was found that the formulas for the solubility parameter were the same, but the linear method produced a slightly different entropy term. The nonlinear method gave a lower correlation coefficient and wider confidence intervals and was more effective at distinguishing systems than the linear model. The effect of the deviation of probes in the solubility parameter model is discussed. Using probes with low solubility parameters to measure the polymer solubility parameter gave wider confidence intervals. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 2894–2902, 2004 相似文献
998.
The purpose of this work was to study how mineral fillers would behave in a polypropylene (PP) matrix when PP modified with maleic anhydride (MA) and/or itaconic acid (IA) was used as a coupling agent in the preparation of mineral‐filled PP composites. The composites were characterized with tensile mechanical measurements and morphological analysis. The optimum amount of the coupling agent to be used to obtain composites with improved mechanical properties was established. The results indicated that these coupling agents enhanced the tensile strength of the composites significantly, and the extent of the coupling effect depended on the nature of the interface that formed. The incorporation of coupling agents enhanced the resistance to deformation of the composite. The behavior of IA‐modified PP as a coupling agent was similar to that of a commercial MA‐modified PP for the filled PP composites. Evidence of improved interfacial bonding was revealed by scanning electron microscopy studies, which examined the surfaces of fractured tensile test specimens; their microstructures confirmed the mechanical results with respect to the observed homogeneous or optimized dispersion of the mineral‐filler phase in these composites. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2343–2350, 2007 相似文献
999.
Although leather has a number of desirable properties such as thermal stability and fire retardancey, in addition to high toughness, it has a few drawbacks such as weight, high water absorption, poor soil and rot resistance, and nonuniformity. If these defects are overcome, leather's usefulness would be further enhanced and its competitive position with respect to synthetics would increase. This study reports the physical and mechanical properties of buffalo leather after chemical graft copolymerization with ethyl acrylate, butyl acrylate, and 2‐ethyl hexyl acrylate using benzoyl peroxide as an initiator. The optimum conditions for grafting (e.g., monomer and initiator concentrations, temperature and time of grafting, and solvent leather ratio) were extensively investigated. The study achieved outstanding properties for buffalo leather in reduction of water uptake after grafting, especially on using 2‐ethyl hexyl acrylate and butyl acrylate monomers. FT‐IR and solid 13C‐NMR for leather before and after grafting confirmed the grafting process.© 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 1478–1483, 2003 相似文献
1000.
Hongcang Zhou Baosheng Jin Zhaoping Zhong Yaji Huang Rui Xiao Youfei Zheng 《Korean Journal of Chemical Engineering》2007,24(3):489-494
The coal partial gasification catalyzed by limestone, sodium carbonate and dolomite was studied using a bench-scale atmospheric
fluidized bed in the presence of air and steam at 900 °C. The effects of limestone, sodium carbonate and dolomite on composition,
heating value, gas yield of product gas and carbon conversion in the catalytic coal partial gasification have been examined.
The experimental results show that the catalysts can effectively improve the gas quality, the heating value and the gas yield
of product gas and carbon conversion. The catalytic effect of sodium carbonate is better than that of limestone and dolomite.
The increase of limestone loading can enhance the quality of product gas, such as the content of combustible gas, the high
heating value and the gas yield, during coal partial gasification.
This work was presented at the 6
th
Korea-China Workshop on Clean Energy Technology held at Busan, Korea, July 4–7, 2006. 相似文献