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991.
新型复合环氧光学树脂的制备与性能研究 总被引:8,自引:0,他引:8
通过2,2-二巯基乙硫醚(MES)与环氧氯丙烷反应合成了2,2-二巯基二乙硫醚二缩水甘油醚型环氧树脂(DGEMES),通过FTIR和MS对其进行表征;用乙二胺作为固化剂,将DGEMES与双酚A型环氧树脂(DGEBA)复合固化,得到了新型高折射率和低色散的光学树脂.DGEMES是一种较好的共聚单体,可以同时提高共聚树脂的折射率和阿贝数;DGEBA/DGEMES/乙二胺共固化树脂的nd=1.59~1.62,νd=35~39;当DGEMES的质量分数为40%时,固化树脂的折射率达到1.60以上,冲击强度22.5kJ/m2,且其它性能较均衡.此外,以甲基六氢苯酐(B-650)为固化剂,还合成了具有中等折射率的DGEBA/DGEMES/B-650共固化树脂(nd=1.54~1.56,νd=38~40),并对其光学和机械性能进行了研究. 相似文献
992.
SDS micelles flocculate in the presence of Al3+, creating an aggregate with pollutant-removing properties. The fraction of SDS micelles flocculating depends on the concentrations
of SDS and Al3+. This paper describes how this fraction also changes with pH. There are two reasons for this dependence: a change in pH has
a strong effect in the solution chemistry of Al3+, converting it into the compound [Al13O4(OH)24]7+, a strong flocculant, or precipitating it as Al(OH)3; and at low pH protons may compete with Al3+ as binding counter-ions for micelles. An increase in pH allows flocculation of SDS at high concentrations of Al3+, which under unmodified pH does not occur. Micelle flocculates are reported in this work to exist between pH 5 and pH 8,
suggesting the potential use of Adsorptive Micellar Flocculation for the removal of anionic pollutants from waste waters not
necessarily limited to acidic solutions.
Received: 18 August 2000 Accepted: 5 October 2000 相似文献
993.
Understanding adsorption phenomena involving humic acids and clays is a difficult challenge owing to their complex nature.
Thus, to progress in the study of such systems, attempts were made to replace natural systems by polyacids and oxides of simpler
chemical and morphological structure. Since the present investigation was dedicated to determine some characteristics of acidic
soils which contain traces of aluminium ions, these ions were added to the adsorbent/polyacid systems as trace constituents.
Phenomena related to the interactions of humic or polyacrylic acid with aluminium oxide and kaolinite clay have been investigated
and the well-differentiated interfacial behaviour of the oxide and kaolinite was determined and discussed. The results of
electrophoretic mobility measurements demonstrated the huge time-dependent effect of polymeric layers adsorbed on oxides and
modified clays.
Received: 24 July 2000 Accepted: 20 December 2000 相似文献
994.
SHI Zuoqing XU Mancai LIN Xue XU Mingcheng FAN Yunge SHI Rongfu YANG Yizhong HE Binglin 《Chinese Journal of Reactive Polymers》2000,(1)
1 INTRODUCTIONPhenol and many substitUted phenols, such as nitrophenols, chlorophenols and aminophenolset al, are the common organic pollutantS existing in wane water of many chemical plants.Treatment of the wastewater containing phenols is an important project for environmentprotection and has been studied by various methods, such as dialysis ['l, microbial degradation ['1,oxidation l'l, extracting with solvents I4] and adsorption with polymeric adsorbents IS]. Theadsorption method is v… 相似文献
995.
XU Zhida ZENG Hanmin FENG Yangqiao Materials Science Institute of Zhongshan University Guangzhou China Research Institute of Guangzhou Petrochemical Complex Guangzhou China 《Chinese Journal of Reactive Polymers》2000,(2)
Sulfideisoneofthemainpollutionsources.Ifthereweremorethiolsingasoline,thiolswouldmakegasolinegivingoffafoulsmellandcausingcorrosionofmetal.Therefore,manycountriessetstrictdemandstothiolscontentingasoline.Ingeneral,thecontentofthiol-sulfuringasolineisrequestedtobelow10ppm.ActivatedCarbonFiber(ACF)isanewkindofecomaterial[1].Itssuperadsorptioncapacitymakesithavewiderandwiderapplicationprospectsinenvironmentalprotection.ThefurtherstudiesonACFareboththeoreticallyandpracticallyimportant.Therear… 相似文献
996.
997.
The industrial porous co-polymers and resins in the form of spherical granules include three main matrices which serve as
the basis of the large-scale production of ion-exchange materials: styrene/divinylbenzene, vinylpyridine/divinylbenzene and
acrylonitrile/divinylbenzene. Complex thermal methods (TG, DTG and DTA) were used to study the carbonization processes of
various industrial products utilized as starting materials for the preparation of synthetic active carbons. The DTG results,
the thermal effects observed during the programmed heating of samples, and the mass-spectrometric and IR-spectroscopic data
up to 800°C provided a picture of a multi-stage carbonization process. This includes the removal of moisture from the polymer
matrices, the primary cross-linking of the chains, their aromatization and condensation due to the cross-linking of polynuclear
structures, and the removal of ‘excess carbon’ as simple molecules and free radicals of hydrocarbon type. The results promoted
the choice of the optimal regimes in which to carryout the isothermal pyrolysis of various polymer matrices and preliminary
chemical modifications to increase the yields on carbon and to prepare synthetic active carbons such as those of SCN, SCAN
and SCS types. General schemes were proposed for the chemical reactions accompanying the carbonization process for these polymer
matrices.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
998.
Changes in density and surface tension of water in silica pores 总被引:3,自引:0,他引:3
T. Takei K. Mukasa M. Kofuji M. Fuji T. Watanabe M. Chikazawa T. Kanazawa 《Colloid and polymer science》2000,278(5):475-480
The density and surface tension of water in small pores of silicas have been investigated. These physical properties of water
in the pores were calculated from a comparison of pore volumes and pore radii which were estimated from adsorption and desorption
isotherms of nitrogen and water. Below a pore radius of about 5 nm both the density and the surface tension of water in the
pores were smaller than those of the bulk liquid and decreased with a decrease in pore size. The density of water in the pores
decreased with an increase in the concentration of surface hydroxyl groups. Similarly the surface tension of water in the
pores is influenced by the surface hydroxyl groups. Anomalous changes in the density and surface tension of the water in the
pores are attributed to the interaction of water molecules with surface hydroxyl groups and hydrogen-bond formation among
water molecules.
Received: 20 April 1999 Accepted in revised form: 17 November 1999 相似文献
999.
1000.