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Silica Core (silica + core)
Selected AbstractsPreparation and Characterization of Uniformly Sized Sub-micrometer Spherical Silica/Organic Polymer Hybrid ParticlesADVANCED ENGINEERING MATERIALS, Issue 9 2003X.-s. Xing Hybrid particles with a core-shell structure, consisting of a silica core and a polyvinyl alcohol (PVA) shell, (see Figure for an SEM image of a particle material of this type), were fabricated via a two-step sol-gel process. The PVA molecular chains are probably physically adsorbed onto the surface of silica cores by hydrogen bonds and van der Waals forces. [source] Synthesis and properties of organic/inorganic hybrid nanoparticles prepared using atom transfer radical polymerizationJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2008Tzong-Liu Wang Abstract The synthesis of organic/inorganic hybrid materials was conducted by atom transfer radical polymerization (ATRP) of styrene and methyl methacrylate (MMA) from the surface of silica colloids. Colloidal initiators were prepared by the functionalization of silica nanoparticles with (3-(2-bromoisobutyryl)propyl) dimethylethoxysilane (BIDS). Well-defined polymer chains were grown from the nanoparticle surfaces to yield individual particles composed of a silica core and a well-defined outer polystyrene (PS) or poly(methyl methacrylate) (PMMA) layer. Fourier transform infrared (FTIR) and solid state 13C and 29Si-NMR spectroscopy confirmed the successful modification of nanosilica surfaces. Subsequent grafting of polymers on silica surfaces by ATRP was also performed with success based on FTIR and NMR data. Scanning electron microscopy (SEM) and silicon mapping showed both hybrid materials were homogeneous dispersion systems. Energy dispersive X-ray spectrometer (EDS) analysis indicated that the BIDS initiator was covalently attached on surfaces of silica nanoparticles and ATRP of styrene and MMA were accomplished. Thermogravimetric analysis (TGA) results displayed higher thermal stabilities for both nanohybrids in comparison with the linear-type vinyl polymers. Contact angle measurements revealed the nanomaterials character for both silica-based hybrid materials. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Hydrothermal Alteration and Cu-Au Mineralization at Nena High Sulfidation-type Deposit, Frieda River, Papua New GuineaRESOURCE GEOLOGY, Issue 4 2002Joseph Onglo Espi Abstract. The Nena Cu-Au deposit, located in the Frieda River mineral district of northwestern mainland Papua New Guinea, is a composite structurally-lithologically controlled high sulfidation (HS) system. Its hydrothermal alteration and Cu-Au mineralization are presented in this paper. Initially propylitized andesitic volcanics veined by epithermal quartz were pervasively superimposed by zoned HS alteration. The zonation grades from vuggy silica core to sulfur-rich, pyritic silica-alunite halo followed by pyrophyllite-dickite-kaolinite interval and finally to thin illite-smectite margin, suggesting progressive decrease in temperature and increase in pH. This zonation is enveloped by chlorite-epidote-calcite-gypsum alteration. The acid altered rocks were then invaded by multiple phases of pyrite, subsequently crosscut by quartz, vein alunite and barite. Then sequential deposition of bladed covellite, enargite, luzonite and stibioluzonite occurred from the NW to the SE portions of the deposit, forming a zonation suggestive of progressive decrease in temperature, sulfur fugacity and sulfidation stage. Most ore mineralization occurs in the vuggy silica core. Gold mineralization commenced from the transition of enargite to luzonite and continued throughout the stibioluzonite stage. Associated with gold deposition are Au-rich pyrite, tennantite-tetrahedrite, chalcopyrite-bornite, native tellurium, electrum, calaverite, bismuthinite and galena. Native sulfur occupied the remaining cavities and represents the waning stage of the hydrothermal system. Fluid inclusions studies distinguished magmatic (>300,350d,C, 9,15 wt% NaCl equiv.) and meteoric (<150,200d,C, 1,2 wt% NaCl equiv.) fluids (Holzberger et al., 1996). Temperatures and salinities of fluid inclusions from barite associated with Cu sulfides show a general decrease from NW (330d,C, 9,15 wt% NaCl equiv.) to SE (172d,C, 10 wt% NaCl equiv.) parts of the deposit, indicating gradual entrainment of ground water (Hitchman and Espi, 1997). Interaction of magmatic fluids with meteoric water accompanied by changes in temperature, salinity, acidity and oxidation state of the resultant fluids is interpreted to have been the main cause of metal precipitation. Finally, supergene processes generated Au zone with an underlying chalcocite-covellite-digenite blanket over the primary sulfides at depth. Gold occurs as lattice constituent in scorodite, limonite-goethite and jarosite. Chalcocite is more abundant and widespread than other Cu sulfides. Acidic fluids deposited powdery alunite and kaolinite, vein alunite and amorphous silica. Weakly secondary biotite-quartz altered porphyry located below the known HS Cu-Au deposit contains chalcopyrite-bornite and is overprinted by quartz-alunite-pyro-phyllite-pyrite assemblage. This feature indicates close temporal, spatial and genetic relation between the two deposit types. [source] Preparation and Characterization of Uniformly Sized Sub-micrometer Spherical Silica/Organic Polymer Hybrid ParticlesADVANCED ENGINEERING MATERIALS, Issue 9 2003X.-s. Xing Hybrid particles with a core-shell structure, consisting of a silica core and a polyvinyl alcohol (PVA) shell, (see Figure for an SEM image of a particle material of this type), were fabricated via a two-step sol-gel process. The PVA molecular chains are probably physically adsorbed onto the surface of silica cores by hydrogen bonds and van der Waals forces. [source] Nanoporous, Ultralow-Dielectric- Constant Fluoropolymer Films from Agglomerated and Crosslinked Hollow Nanospheres of Poly(pentafluorostyrene)- block -Poly(divinylbenzene)ADVANCED MATERIALS, Issue 21 2005G.-D. Fu Nanoporous fluoropolymer films with dielectric constants below 2 are prepared via consecutive surface-initiated atom transfer radical polymerizations of pentafluorostyrene (PFS) and divinylbenzene (DVB) on silica nanospheres. After agglomeration of the nanospheres, crosslinking of the nanospheres by UV, and removal of the silica cores (see Figure), a nanoporous fluoropolymer film with a dielectric constant as low as 1.7 is formed. [source] A novel and facile preparation method of hollow silica spheres containing small SiO2 coresJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 15 2007Xinjian Cheng Abstract This article presents a novel and facile preparation method of hollow silica spheres with loading small silica inside. In this approach, positively charged SiO2/polystyrene core-shell composite particles were synthesized first, when the silica shells from the sol-gel process of tetraethoxysilane were then coated on the surfaces of composite particles via electrostatic interaction, the polystyrene was dissolved subsequently even synchronously in the same medium to form hollow silica spheres with small silica cores. TEM, SEM, and FTIR measurements were used to characterize these composite spheres. Based on this study, some inorganic or organic compounds could be loaded into these hollow silica spheres. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 3431,3439, 2007 [source] | ||||||||||||||||||||||