液封液桥内热毛细对流的数值模拟

建立了液封液桥(不相溶混的双层同轴液柱)内热毛细对流的物理数学模型,采用涡量-流 函数法、利用有限差分格式对微重力条件下液封液桥内热毛细对流进行了数值模拟,得到了 双层液柱主流区的温度场和流场,证实了液封技术能削弱液桥主流区的热毛细对流,从而提 高浮区晶体生长质量,找出了液封厚度以及内、外层流体物性参数比对液桥内热毛细对流的 影响规律.     

Encapsulation of Bromocresol Green pH Indicator into a Sol‐Gel Matrix

The bromocresol green pH indicator was encapsulated into transparent monolithic silica matrices using acid catalyzed sol‐gel reaction. Tetraethylorthosilicate was used for the entrapment of the bromocresol green indicator. The immobilized bromocresol green shows behavior similar to its solution counterpart. It retains its structure during the sol‐gel reactions in terms of response to pH and albumine. The polarized light microscopy has indicated that the bromocresol green molecules are strongly interacted within the host silica network.     

Core–shell‐type multiarm star polyethylenimine‐block‐poly(ε‐caprolactone): Synthesis and guest encapsulation potential

Novel multiarm star copolymers with poly(?‐caprolactone) (PCL) as the arms and hyperbranched polyethylenimine (HPEI) as the core have been successfully prepared by the tin(II) 2‐ethylhexanoate catalyzed ring‐opening polymerization of ?‐caprolactone (CL) with HPEI used directly as a macroinitiator. Not only primary but also secondary amine groups of HPEI participate in initiating the ring‐opening polymerization of CL with almost 100% initiation efficiency. The average degree of polymerization of the PCL arms can be controlled by the feed ratio of the monomers to the initiating sites. Because of the polarity difference of the PCL arms and HPEI core, the obtained multiarm star polymers display an inverted micellar structure with potential extraction and encapsulation of water‐soluble guests. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4165–4173, 2006     

碱土铝酸盐系长余辉粉表面包膜的探讨

简介了长余辉发光材料的发光原理,主要讨论包覆温度、包覆时间及pH值对比表面积、包膜量的影响,从实验中找出最佳的工艺包覆条件。     

Promotion of Proton Conductivity by Encapsulation of Metal-Organic Polyhedra in Metal-Organic Frameworks

A Zr-based metal-organic polyhedron (MOP) was self-assembled in a porous MOF host, DUT-68, successfully to synthesize MOP-1@DUT-68. The MOP guest (MOP-1) has a diameter of about 20 Å, larger than that of the square windows (pore sizes of ∼14 Å) of DUT-68 but smaller than that of the rhombicuboctahedral cage (27.7 Å), which means that the migration and leaching of MOP-1 could be effectively prohibited if MOP-1 is encapsulated in the MOF′s cavities. The proton conductivity of MOP-1@DUT-68 is 1.14×10⁻³ S cm⁻¹ (at 80 °C under 98 % relative humidity), which is three orders of magnitude higher than that of DUT-68. Compared with MOP-1⊂DUT-68, which was synthesized by impregnation, MOP-1@DUT-68 is more prone to form faster proton-conduction pathways and thus provides higher proton conductivity.     

Terpyridine-Based 3D Metal–Organic-Frameworks: A Structure–Property Correlation

Design, synthesis, and applications of metal–organic frameworks (MOFs) are among the most salient fields of research in modern inorganic and materials chemistry. As the structure and physical properties of MOFs are mostly dependent on the organic linkers or ligands, the choice of ligand system is of utmost importance in the design of MOFs. One such crucial organic linker/ligand is terpyridine (tpy), which can adopt various coordination modes to generate an enormous number of metal–organic frameworks. These frameworks generally carry physicochemical characteristics induced by the π-electron-rich (basically N-electron-rich moiety) terpyridines. In this minireview, the construction of 3D MOFs associated with symmetrical terpyridines is discussed. These ligands can be easily derivatized at the lateral phenyl (4′-phenyl) position and incorporate additional organic functionalities. These functionalities lead to some different binding modes and form higher dimensional (3D) frameworks. Therefore, these 3D MOFs can carry multiple features along with the characteristics of terpyridines. Some properties of these MOFs, like photophysical, chemical selectivity, photocatalytic degradation, proton conductivity, and magnetism, etc. have also been discussed and correlated with their frameworks.