简介：

简介：hard-core/soft-shell钙碳酸盐(CaCO3)的合成/poly(甲基methacrylate)(PMMA)混合结构化的nanoparticles(<100nm)由把分裂成原子的微乳液聚合，过程被报导。聚合物链通过acoupling代理人的使用被抛锚到nano-CaCO3的表面上，triethoxyvinylsilane(TEVS)。铵persulfate(APS)，钠dodecyl硫酸盐(SDS)和n-pentanol分别地被用作开始者，表面活化剂和cosurfactant。coreshell乳胶粒子的聚合机制被讨论。由PMMA的nano-CaCO3的封装用一台传播电子显微镜(TEM)被证实。coreshell粒子的grafting百分比被thermogravimetric分析(TGA)调查。nano-CaCO3/PMMAcoreshell粒子被Fourier变换描绘红外线(FTIR)光谱学和微分扫描热量测定(DSC)。FTIR结果在nano-CaCO3粒子和PMMA的接口揭示了一个强壮的相互作用的存在，它成功地暗示聚合物链是grafted到通过联合代理人的连接的nano-CaCO3粒子的表面上。另外，TGA和DSC结果与纯nano-PMMA的相比显示了coreshell材料的热稳定性的改进。nano-CaCO3/PMMA粒子被混合进聚丙烯(PP)矩阵由融化处理。它能也用扫描PMMA锁住的电子显微镜学(SEM)被观察grafted在聚合物矩阵(PP矩阵)防碍到CaCO3nanoparticles上CaCO3的聚集并且因此与PP矩阵改进CaCO3nanoparticles的相容性。

简介：PureAl2O3-2SiO2powderswerepreparedbysol-gelandcoprecipitationmethods,andtheiralkaliactivationreactivitieswerecompared.Thealkali-activationreactivityofthepowderpreparedbythesol-gelmethodwashigherthanthatofthepowderpreparedbythecoprecipitationmethod.Thepowderswereinvestigatedby27AIand29Simagic-anglespinningnuclearmagneticresonancespectroscopy（MASNMR）tounderstandtherelationshipbetweentheirstructureandalkali-activationreactivity.The27AlMASNMRdatashowedthatthefive-coordinateAIcontentofthepowderpreparedbythesol-gelmethodwashigherthanthatofthepowderpreparedbycoprecipitation.Thehighercontentoffive-coordinateAlcorrespondedtohigheralkali-activationreactivity.The29SiMASNMRdatashowedthatforthepowderpreparedbythesol-gelmethod,siliconwasreplacedbyaluminumatsecondarycoordinationsitesofthecentralSiatomsduringcalcination.However,forthepowderpreparedbysingle-batchcoprecipitation,themainchangewasfromalowdegreeofpolycondensationtoahighdegreeofpolycondensation.