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991.
992.
Pickering乳滴模板法制备有机/无机杂化的核壳微球越来越引起人们的关注,主要因为该方法制备出的微球具有以无机粒子为壳层的超粒子结构(supracolloidal structure),能够赋予微球独特的功能.胶体粒子在乳滴表面自组装形成有序的球面胶体壳,得到稳定Pickering乳液,固定乳滴表面的胶体粒子来制备核壳结构的微球或者以胶体粒子为壳层的微胶囊(colloidosome).本文综述了我们课题组以Pickering乳滴模板法制备超粒子结构有机/无机杂化微胶囊包括实心微球方面的工作.我们选择具有不同性能、种类的胶体粒子以及具有不同性质和功能的核材料,采用Pickering乳滴模板法,对吸附在乳滴表面的胶体粒子用不同的固定方法制备具有不同结构和性能的微球和微胶囊,利用基于多重Pickering乳液的聚合技术制备双纳米复合的超粒子结构多核聚合物微球. 相似文献
993.
In this study, CoFe2O4/Sawdust and NiFe2O4/Sawdust magnetic nanocomposites were synthesized using a hydrothermal method, and then characterized using X-ray powder diffraction, Infrared, scanning electron microscopy, Brunauer–Emmett–Teller/Barrett–Joyner–Halenda, and vibrating-sample magnetometer techniques. In this study, unmodified sawdust (US), modified sawdust (MS), unmodified CoFe2O4/sawdust (UCS), modified CoFe2O4/sawdust (MCS), unmodified NiFe2O4/sawdust (UNS), and modified NiFe2O4/Sawdust (MNS) magnetic nanocomposites, which are inexpensive, economical, environmentally friendly absorbents, and have a high selective hydrophobic, were used for the removal of oil from the water surface. The results show that the UCS, MCS, UNS, and MNS magnetic nanocomposites can selectively absorb the oil spreading on the water surface, due to its superhydrophobicity and superoleophilicity, and can be easily collected from water under the influence of a magnetic field. In addition, the results showed that the absorbents reach their equilibrium at the 30-min mark. Among all the absorbents, the MNS magnetic nanocomposite showed the maximum absorption capacity (18.172 g/g) at the 40-min mark. The results of the kinetic studies showed that the second-order kinetic equation with the highest correlation coefficient had the best fit with the experimental results. 相似文献
994.
以溶于十八烯的Se作为Se前驱体,在无膦条件下制备得到了具有较高量子产率的Mn:ZnSe纳米晶.为了进一步提高纳米晶的稳定性和发光强度,运用外延生长的方法进行ZnS壳层包覆并得到了具有核-壳结构的Mn:ZnSe/ZnS纳米晶.X射线衍射、透射电子显微镜及吸收和荧光光谱测试结果表明,该方法合成的Mn:ZnSe纳米晶以及核-壳结构Mn:ZnSe/ZnS纳米晶均为闪锌矿结构,具有良好的单分散性,包覆ZnS外壳层后量子产率可达到60%以上.此外,对ZnS壳层厚度和Mn2+的掺杂量对Mn:ZnSe/ZnS纳米晶发光强度的影响及发光机制也进行了初步讨论. 相似文献
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A silane‐modified mono‐lacunary Keggin‐type polyoxometalate (POM), (Bu4N)4[SiW11O39{(CH2?CH? Si)2O}] (SiW11? CH?CH2), was obtained by reaction of vinyltrimethoxysilane with K8(SiW11O39) in acidic MeCN/H2O mixed solutions. Then, the modified polyoxometalate was physically blended with the pyromellitic dianhydride (PMDA)‐4,4′‐oxydianiline (ODA) poly(amic acid) and the blends were thermally imidized to form polyimide/ polyoxometalate composites. The X‐ray diffraction (XRD) analysis indicates that the polyoxometalate clusters cannot form crystalline structures in the composite, suggesting that the blending leads to improved compatibility between the polymer matrix and the modified polyoxometalate. The EDS (W‐mapping) studies on the composite films reveal that the polyoxometalate clusters are well dispersed in the polyimide matrix. The physical incorporation of modified POM into polyimide remarkably reduced the dielectric constant of the latter from 3.29 to 2.05 when 20 wt% of SiW11? CH?CH2 was used. Besides, the addition of the modified POM into polyimide increased the storage modulus of polyimide without severely affecting its thermal properties. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
1000.
In this study the curing kinetics of epoxy based on the diglycidyl ether of bisphenol A (DGEBA), 4,4′‐diaminodiphenyl sulfone (DDS) as a hardener, and SiO2/TiO2 (70:30) as a nanofiller was investigated by nonisothermal differential scanning calorimetry (DSC). The effects of different weight contents of SiO2/TiO2 nanoparticles were studied using DSC in Dynamic Mode and the best value of the nanofiller was found to be 5 phr (parts per hundred). Dynamic measurements were used to obtain the total heat of reaction of the epoxy system as well as its activation energy (Ea) based on the isoconversional methods of Kissinger and Ozawa. The process revealed a dependence of the activation energy on conversion (α). The morphology of the cured system was investigated by scanning electron microscopy (SEM). It showed a strong cross‐linking between the resin and hardner and a relatively better dispersion of surface modified filler nanoparticles. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献