首页 | 官方网站   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   15012篇
  免费   1061篇
  国内免费   224篇
工业技术   16297篇
  2024年   36篇
  2023年   126篇
  2022年   131篇
  2021年   243篇
  2020年   258篇
  2019年   276篇
  2018年   244篇
  2017年   331篇
  2016年   372篇
  2015年   427篇
  2014年   690篇
  2013年   697篇
  2012年   931篇
  2011年   1042篇
  2010年   782篇
  2009年   913篇
  2008年   848篇
  2007年   1009篇
  2006年   1086篇
  2005年   901篇
  2004年   807篇
  2003年   718篇
  2002年   564篇
  2001年   487篇
  2000年   394篇
  1999年   398篇
  1998年   303篇
  1997年   251篇
  1996年   161篇
  1995年   149篇
  1994年   134篇
  1993年   148篇
  1992年   107篇
  1991年   75篇
  1990年   44篇
  1989年   53篇
  1988年   27篇
  1987年   14篇
  1986年   13篇
  1985年   22篇
  1984年   26篇
  1983年   20篇
  1982年   26篇
  1980年   4篇
  1975年   1篇
  1974年   1篇
  1951年   7篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
91.
LLDPE及其催化剂技术进展   总被引:3,自引:0,他引:3  
综述了线性密度聚乙烯(LLDPE)研究的最进展情况,特别对乙烯原位聚合工艺和后过渡金属镍、钯催化剂进行了详细的叙述,对我国LLDPE的生产提出了自己的看法。  相似文献   
92.
取样光栅周期中等效啁啾的实验研究   总被引:2,自引:0,他引:2  
在Moire取样Bragg光纤光栅(SBG)的理论基础上,首次通过用相位模板旋转和2次曝光的方法,得出了带有取样啁啾的SBG的各个Fourier级数的等效啁啾率。实验数据和理论值的误差小于9%。  相似文献   
93.
Halogen-induced charge transfer polymerization of pyrrole in aqueous media   总被引:1,自引:0,他引:1  
E.T. Kang  T.C. Tan  K.G. Neoh  Y.K. Ong 《Polymer》1986,27(12):1958-1962
Simultaneous polymerization and doping of pyrrole have been carried out in the presence of a halogenic electron acceptor, bromine (Br2) or iodine (I2), in aqueous dispersion or in a two-phase solvent system. The morphology of the polypyrrole (PPY) so produced is granular and porous. The electrical conductivity of the PPY-I2 charge transfer (CT) complex is of the order of 101 ohm−1 cm−1 while that of the PPY-Br2 complex is about one order of magnitude less. Both complexes are stable in the atmosphere. The physicochemical properties of the PPY-I2 and PPY-Br2 CT complexes prepared under various experimental conditions are examined in detail.  相似文献   
94.
本文采用反相微乳液聚合的方法合成了丙烯酰胺(AM)/丙烯酰氧基乙基三甲基氯化铵(AD-AMQUAT)/聚氧乙烯大单体(PEO-A)/N,N'-亚甲基双丙烯酰胺(Bis)的四元共聚物微粒.研究了该微粒助留剂的结构与性能.这种微粒和纸纤维能够通过离子键和氢键作用显著地增强助留效果.  相似文献   
95.
Free radical emulsion polymerization of methyl methacrylate (MMA) and 2‐ethylhexyl acrylate (EHA) results in the synthesis of pressure‐sensitive adhesives (PSAs) with good tack properties. Management of both the copolymer composition and the polymerization process allows one to control the behavior of the PSA. Semicontinuous (SC) processes create polymer particles whose instantaneous composition is close to that of the feed particle The SC Mixture process (continuous feeding with comonomer blends) affords nearly homogeneous latex particles and PSA films. The SC Gradient process (separate feedings at inversely varying rates) affords heterogeneous particles and films. The Batch process leads to somewhat heterogeneous films, but the hard (MMA‐rich) microdomains are made compatible with their soft (EHA‐rich) matrix because of the assumed formation of tapered‐type copolymers. Tack measurements indicate the importance of the particle and film structures. Too much hardness or softness leads to unacceptable lacks of adhesion and cohesion, respectively. Homogeneous structures prove adequate, but their tack properties collapse with rising temperature. Heterogeneous structures, with extensive phase segregation, prove unsatisfactory because they lack adhesion and cohesion. Finally, the association of well‐balanced composition and compatible heterogeneity is the criterion for suitable PSA behavior. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 2749–2756, 2003  相似文献   
96.
磁性聚乙烯醇缩丁醛微球的制备和性质   总被引:2,自引:0,他引:2  
运用乳化复合技术制备出磁性聚乙烯醇缩丁醛微球。该微球呈珠状 ,平均粒径为10~ 2 0nm ,具有较大的蛋白质固载量 ,可作为载体对多种酶及蛋白质加以固定。并研究了磁性聚乙烯醇缩丁醛微球制备条件、吸附时间、pH值等对磁性聚乙烯醇缩丁醛微球固定蛋白载量的影响  相似文献   
97.
丙烯酸酯与甲基丙烯酸酯的共聚及性能研究   总被引:22,自引:0,他引:22  
采用悬浮聚合法,以丙烯酸-2-乙基-己酯与甲基丙烯酸十二酯为单体,合成了共聚型高吸油性树脂。研究了共聚单体的配比、交联剂用量、引发剂用量诸因素对高吸油性树脂的性能影响。制得的树脂可以吸其自身质量的11.8倍的煤油、14.7倍的苯、6.5倍的泵油。  相似文献   
98.
In the research presented here, we explore the use of a low‐energy plasma to deposit thin silicone polymer films using tetramethyldisiloxane (TMDSO) (H(CH3)2? Si? O? Si? (CH3)2H) on the surface of an ethylene propylene diene elastomeric terpolymer (EPDM) in order to enhance the surface hydrophobicity, lower the surface energy and improve the degradation/wear characteristics. The processing conditions were varied over a wide range of treatment times and discharge powers to control the physical characteristics, thickness, morphology and chemical structure of the plasma polymer films. Scanning electron microscopy (SEM) shows that pore‐free homogeneous plasma polymer thin films of granular microstructure composed of small grains are formed and that the morphology of the granular structure depends on the plasma processing conditions, such as plasma power and time of deposition. The thicknesses of the coatings were determined using SEM, which confirmed that the thicknesses of the deposited plasma‐polymer films could be precisely controlled by the plasma parameters. The kinetics of plasma‐polymer film deposition were also evaluated. Contact angle measurements of different solvent droplets on the coatings were used to calculate the surface energies of the coatings. These coatings appeared to be hydrophobic and had low surface energies. X‐ray photoelectron spectroscopy (XPS) and photoacoustic Fourier‐transform infrared (PA‐FT‐IR) spectroscopy were used to investigate the detailed chemical structures of the deposited films. The optimum plasma processing conditions to achieve the desired thin plasma polymer coatings are discussed in the light of the chemistry that takes place at the interfaces. Copyright © 2004 Society of Chemical Industry  相似文献   
99.
底排弹射击密集度的试验研究   总被引:1,自引:0,他引:1  
底排弹底排装置的工作特性对底排弹的距离散布有着明显的影响。本文以初步的静态和飞行试验结果为依据,讨论了利用现有试验手段对底排因素引起的距离散布进行分析和计算的方法,并在此基础上提出了减小底排弹距离散布的途径。  相似文献   
100.
The ring-opening polymerization of hexamethylcyclodisilazane (D2NMe), initiated by methyl triflate in 1,2-dichloroethane, forms in the first, fast kinetic step both linear polymer and cyclic dimer (D4NMe). Subsequently a slow depolymerization process occurs leading to exclusively cyclotrisilazane (D3NMe). On the basis of kinetic measurements carried out using an adiabatic calorimetric technique and complementary experiments, mechanisms of both propagation, cyclization and back-biting reactions are proposed. The influence of the reaction temperature was also studied; it is demonstrated that, at low temperature, polymerization does not lead to cyclic oligomer formation. In such conditions, the polymerization presents a ‘living’ character.  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-23

京公网安备 11010802026262号