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Silica Nanoparticles (silica + nanoparticle)
Kinds of Silica Nanoparticles Selected AbstractsChemInform Abstract: One-Step, Three-Component Synthesis of Highly Substituted Pyridines Using Silica Nanoparticle as Reusable Catalyst.CHEMINFORM, Issue 13 2010Subhash Banerjee Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source] Kinetics of adsorption of 2-CEES and HD on impregnated silica nanoparticles under static conditionsAICHE JOURNAL, Issue 5 2009Amit Saxena Abstract Silica nanoparticles of high surface area (887.3 m2/g) were synthesized using aerogel route and, thereafter, impregnated with those reactive chemicals, which have already been proven to be effective against sulfur mustard (HD). Thus, developed adsorbents were tested for their potential by conducting studies on kinetics of adsorption of 2-chloroethylethyl sulfide (2-CEES) and HD under static conditions. Kinetics of adsorption was studied using linear driving force model and Fickian diffusion model. The kinetic parameters such as equilibration constant, equilibration capacity, diffusional exponent, and adsorbate-adsorbent interaction constant were also determined. Trichloroisocyanuric acid impregnated silica nanoparticles (10% w/w) showed the maximum uptake of 2-CEES (1824 mg/g) and HD (1208 mg/g). Values of diffusional exponent indicated the mechanisms to be Fickian and anomalous. Chemical interaction seemed to be another mechanism involved in the toxicant uptake rate. Hydrolysis, dehydrochlorination, and oxidation reactions were found to be the route of degradation of toxicants. © 2009 American Institute of Chemical Engineers AIChE J, 2009 [source] Nanoparticle formation through solid-fed flame synthesis: Experiment and modelingAICHE JOURNAL, Issue 4 2009W. Widiyastuti Abstract The preparation of silica nanoparticles through solid-fed flame synthesis was investigated experimentally and theoretically. Monodispersed submicrometer- and micrometer-sized silica powders were selected as solid precursors for feeding into a flame reactor. The effects of flame temperature, residence time, and precursor particle size were investigated systematically. Silica nanoparticles were formed by the nucleation, coagulation, and surface growth of the generated silica vapors due to the solid precursor evaporation. Numerical modeling was conducted to describe the mechanism of nanoparticle formation. Evaporation of the initial silica particles was considered in the modeling, accounting for its size evolution. Simultaneous mass transfer modeling due to the silica evaporation was solved in combination with a general dynamics equation solution. The modeling and experimental results were in agreement. Both results showed that the methane flow rate, carrier gas flow rate, and initial particle size influenced the effectiveness of nanoparticle formation in solid-fed flame synthesis. © 2009 American Institute of Chemical Engineers AIChE J, 2009 [source] Structural estimation of particle arrays at air,water interface based on silica particles with well-defined and highly grafted poly(methyl methacrylate)POLYMER ENGINEERING & SCIENCE, Issue 6 2010Jung-Min Moon Silica nanoparticles with well-defined, highly grafted dense poly(methyl methacrylate) (MMA) were prepared by surface-initiated activators regenerated by electron transfer for atom transfer radical polymerization (ARGET ATRP) of methyl methacrylate with an initiator-fixed silica particle in the presence of air. Two different polymerizations of MMA were carried out under the same conditions using tris[2-(dimethylamino)ethyl]amine (Me6TREN) and N,N,N,,N,,N,-pentamethyldiethylene-triamine (PMDETA) as the ligand, respectively. In the CuCl2/PMDETA system, polymerization appeared to be more controlled with a lower polydisperisty compared with the CuCl2/Me6TREN system. The monolayer of these particles was formed at the air,water interface using Langmuir-Blodgett (LB) technique. Multilayers of the particles were fabricated by repetition of LB depositing. A surface pressure,area (,,A) measurement and SEM observation were used to characterize the particle arrays. POLYM. ENG. SCI., 2010. © 2009 Society of Plastics Engineers [source] Glutathione-Induced Intracellular Release of Guests from Mesoporous Silica Nanocontainers with Cyclodextrin GatekeepersADVANCED MATERIALS, Issue 38 2010Hyehyeon Kim Cyclodextrins tethered onto a mesoporous silica nanoparticle via disulfide stalking are effective gatekeepers not only to entrap guest molecules in the pore but also to release the guest in response to glutathione (GSH). The PEGylated nanocontainers also exhibit efficient GSH-mediated release of doxorubicin in cancer cells. Our approach offers unique applications for multifunctional delivery systems. [source] Immobilization of flame retardant onto silica nanoparticle surface and properties of epoxy resin filled with the flame retardant-immobilized silicaJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 22 2009Takeshi Yamauchi Abstract To prepare silica nanoparticle having flame retardant activity, the immobilization of flame retardant onto hyperbranched poly(amidoamine) (PAMAM)-grafted silica was investigated. Grafting of PAMAM onto a silica surface was achieved in a solvent-free dry-system using PAMAM dendrimer synthesis methodology. The immobilization of bromine flame retardant, poly(2,2,,6,6,-tetrabromobisphenol-A) diglycidyl ether (PTBBA), was successfully achieved by the reaction of terminal amino groups of PAMAM-grafted silica (Silica-PAMAM) with epoxy groups of PTBBA. The immobilization of PTBBA was confirmed by FTIR and thermal decomposition GC-MS. The amount of PTBBA immobilized onto Silica-PAMAM was determined to be 60 wt %. PTBBA-immobilized Silica-PAMAM (Silica-PAMAM-PTBBA) was dispersed uniformly in a epoxy resin, and the epoxy resin was cured in the presence of hexamethylenediamine. Flame retardant activity of the epoxy resin filled with Silica-PAMAM-PTBBA was estimated by limiting oxygen index (LOI). The LOI of epoxy resin filled with Silica-PAMAM-PTBBA was higher than that filled with untreated silica and free PTBBA. It was confirmed that the flame retardant activity of epoxy resin was improved by the addition of the Silica-PAMAM-PTBBA. The elimination of PTBBA from the epoxy resin filled with Silica-PAMAM-PTBBA into boiling water was hardly observed by immobilization of PTBBA onto silica surface. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 6145,6152, 2009 [source] Study of the MR relaxation of microglia cells labeled with Gd-DTPA-bearing nanoparticlesCONTRAST MEDIA & MOLECULAR IMAGING, Issue 3 2009Emeline Julie Ribot Abstract Therapies involving cells as vehicles need to visualize in situ the trafficking of the cells concerned. This cellular imaging can be driven by cell contrast agent-based nanoparticle internalization and non-invasive MRI (magnetic resonance imaging) detection. Here, microglial cells, that would transport a suicide gene to a glioma, were incubated for different times, with various concentrations of silica nanoparticles on which numerous Gd-DTPA were grafted. The goal of this study was to investigate the repartition of cell-associated particles. MRI was used to quantitatively follow the particle uptake process. Fluorescence microscopy images showed that, although most of the nanoparticles were internalized, some remained adsorbed on the extracellular membrane surface. The cells were then submitted to various treatments: glycine to release bound nanoparticles and/or ultrasound to destroy the cell membranes. The R1 relaxation rates were measured at 4.7 T. R1 was maximal for 4,h of incubation, decreased after 8,h and remained stable for the 24 following hours. The magnetic resonance signal of ultrasonicated and glycine-treated cells made it possible to quantify the loss of bound nanoparticles after 8,h. Nevertheless, this release did not prevent cell detection since the internalized nanoparticles are enough concentrated to visualize the labeled cells even after 4 days of cell growth. These results highlight the compartmentalization of nanoparticles in microglia and the evolution of the MR signal of the labeled cells. This study could be of importance to interpret in vivo the MR signal changes that could occur after administration of such nanoparticle-labeled cells in therapeutic strategies. Copyright © 2009 John Wiley & Sons, Ltd. [source] Comparison of DNA-Reactive Metabolites from Nitrosamine and Styrene Using Voltammetric DNA/Microsomes SensorsELECTROANALYSIS, Issue 9 2009Sadagopan Krishnan Abstract Voltammetric sensors made with films of polyions, double-stranded DNA and liver microsomes adsorbed layer-by-layer onto pyrolytic graphite electrodes were evaluated for reactive metabolite screening. This approach features simple, inexpensive screening without enzyme purification for applications in drug or environmental chemical development. Cytochrome P450 enzymes (CYPs) in the liver microsomes were activated by an NADPH regenerating system or by electrolysis to metabolize model carcinogenic compounds nitrosamine and styrene. Reactive metabolites formed in the films were trapped as adducts with nucleobases on DNA. The DNA damage was detected by square-wave voltammetry (SWV) using Ru(bpy) as a DNA-oxidation catalyst. These sensors showed a larger rate of increase in signal vs. reaction time for a highly toxic nitrosamine than for the moderately toxic styrene due to more rapid reactive metabolite-DNA adduct formation. Results were consistent with reported in vivo TD50 data for the formation of liver tumors in rats. Analogous polyion/ liver microsome films prepared on 500,nm silica nanoparticles (nanoreactors) and reacted with nitrosamine or styrene, provided LC-MS or GC analyses of metabolite formation rates that correlated well with sensor response. [source] Direct and Rapid Detection of Diphtherotoxin via Potentiometric Immunosensor Based on Nanoparticles Mixture and Polyvinyl Butyral as MatrixesELECTROANALYSIS, Issue 24 2005Dianping Tang Abstract In this paper a novel potentiometric immunosensor for direct and rapid detection of diphtherotoxin (D-Ag) has been developed by means of self-assembly of monoclonal diphtheria antibody (D-Ab) onto a platinum electrode based on nanoparticles mixture (containing gold nanoparticles and silica nanoparticles) and polyvinyl butyral (PVB) as matrixes. At first, D-Ab was absorbed onto the surface of nanoparticles mixture, and then they were entrapped into polyvinyl butyral sol-gel network on a platinum electrode. The detection is based on the change in the potentiometric response before and after the antigen-antibody reaction in a phosphate buffer solution (pH,7.0). The immobilized D-Ab exhibited direct potentiometric response toward D-Ag. In comparison to the conventional applied methods, this strategy could allow antibodies immobilized with higher loading amount and better retained immunoactivity, as demonstrated by potentiometric response, cyclic voltammetry and electrochemical impedance spectroscopy of the immunosensor. The immunosensor with nanoparticles mixture exhibited much higher sensitivity, better reproducibility, and long-term stability than that with gold nanoparticles or silica nanoparticles alone. The linear range was from 5.0×10,3 to 1.2,,g,mL,1 with a detection limit of 1.1×10,3,,g,mL,1. Up to 16 successive assay cycles with retentive sensitivity were achieved for the probes regenerated with in 0.2,mol,L,1 glycine-hydrochloric acid (Gly-HCl) buffer solution and 0.25,mol,L,1 NaCl. Moreover, the immunosensor with nanoparticles mixture was applied to evaluate a number of practical specimens with potentiometric results in acceptable agreement with those given by the ELISA method, implying a promising alternative approach for detecting diphtherotoxin in the clinical diagnosis. [source] Capillary electrophoretic separation of biologically active amines and acids using nanoparticle-coated capillariesELECTROPHORESIS, Issue 9 2008Yu-Fen Huang Abstract This manuscript describes dynamic coating of capillaries with poly(L -lysine) (PLL) and silica nanoparticles (SiO2 NPs) and use of the as-prepared capillaries for the separation of biogenic amines and acids by CE in conjunction with LIF detection. The directions of EOF are controlled by varying the outmost layer of the capillaries with PLL and SiO2 NPs, respectively. Over the pH range 3.0,5.0, the (PLL,SiO2NP)n,PLL capillaries have an EOF toward the anodic end and are more suitable for the separation of acids with respect to speed, while the (PLL,SiO2NP)n capillaries have an EOF toward the cathodic end and are more suitable for the separation of biogenic amines regarding speed and sensitivity. The separations of standard solutions containing five amines and two acids by CE with LIF detection using (PLL,SiO2NP)2,PLL and (PLL,SiO2NP)3 capillaries were accomplished within 10 and 7,min, providing plate numbers of 3.8 and 5.0×104,plates/m for 5-hydroxytryptamine (5-HT), respectively. The LODs for 5-HT and 5-hydroxyindole-3-acetic acid (5-HIAA) are 32 and 2,nM and 0.2 and 1.5,nM when using the (PLL,SiO2NP)2,PLL and (PLL,SiO2NP)3 capillaries, respectively. Identification and quantification of 5-HIAA, homovanillic acid, and DL -vanillomandelic acid in urine samples from a male before and after drinking green tea were tested to validate practicality of the present approach. The results show that the (PLL,SiO2NP)2,PLL capillary provides greater resolving power, while the (PLL,SiO2NP)3 capillary provides better sensitivity, higher efficiency, and longer durability for the separation of the amines and acids. [source] Synthesis, Characterisation and Optical Properties of Silica Nanoparticles Coated with Anthracene Fluorophore and Thiourea Hydrogen-Bonding SubunitsEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 36 2008Pilar Calero Abstract Bifunctionalised hybrid silica nanoparticles have been synthesised and characterised, and their optical emission properties in the presence of certain anions in acetonitrile solutions have been studied. The alkoxysilane derivatives N -butyl- N, -[3-(trimethoxysilyl)propyl]thiourea (1), N -phenyl- N, -[3-(trimethoxysilyl)propyl]thiourea (2) and 3-[(anthracen-10-yl)methylthio]propyltriethoxysilane (3) were prepared and used to functionalise uncoated LUDOX silica nanoparticles with a mean diameter of 18,±,2 nm. The functionalisation of the nanoparticle surfaces was carried out by two different approaches. The first approach relies on the consecutive grafting of the two subunits. In this protocol, the nanoparticles were first functionalised with anthracene derivative 3 (solid NA), and then treated with the corresponding binding sites 1 or 2 to result in the NA-Pt3 and NA-Bt3 solids. The second approach deals with the simultaneous grafting of 1 or 2 and the signalling subunit 3 in different ratios. This method was used for the preparation of the NA1Pt1, NA1Bt1, NA1Pt3 and NA1Bt3 nanoparticles. The bifunctionalised silica nanoparticles were characterised by using standard techniques. Acetonitrile suspensions of NA nanoparticles (5 mg in 20 mL) showed anthracene bands centred at ca. 350, 370 and 390 nm. Upon excitation at 365 nm, a typical emission band with fine structure in the 390,450 nm range was observed. Similar absorption and emission spectra were found for the bifunctionalised nanoparticles. The work is completed with a prospective study of the fluorescence of the prepared nanoparticles in the presence of organic (acetate, benzoate) and inorganic (F,, Cl,, Br,, CN,, HSO4, and H2PO4,) anions. The apparent binding constants (adsorption constants) for the interaction of NA-Pt3 with anions in acetonitrile were determined by performing a Langmuir-type analysis of fluorescence titration data.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) [source] Different Morphological Organic,Inorganic Hybrid Nanomaterials as Fluorescent Chemosensors and Adsorbents for CuII IonsEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 10 2008Soo Jin Lee Abstract Functionalized silica nanotubes (FSNT), functionalized mesoporous silica (FMS), and functionalized silica nanoparticles (FSNP-15) with an immobilized phenanthroline moiety as a fluorescent receptor were fabricated by a sol,gel reaction, and their binding abilities with metal ions were evaluated by fluorophotometry in water/acetonitrile (8:2, v/v) at pH 7. They selectively recognized Cu2+ ions among other metal cations such as Co2+, Cd2+, Hg2+, Ni2+, Fe3+, Ag+, Pb2+, and Zn2+, because the Cu2+ ion selectively binds to the nitrogen atoms of the phenanthroline moiety. Among the three silica nanomaterials with the immobilized receptor 1, the sensitivity of FSNT for Cu2+ ions is better than those of FMS and FSNP-15, indicating that the adsorption capacity for metal ions is dependent on the shape and surface area of the supporting nanomaterials. FSNT (10 mg) adsorb 75,% of the Cu2+ ions (2.0,×,10,4 mM) while FSNP-15 (10 mg) adsorb only 36,%. The detection limit of FSNT for Cu2+ ions was ca. 3.0,×,10,8M. FSNT and FMS can be easily renewed by treatment with a solution of HCl and tetrabutylammonium hydroxide. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) [source] Synthesis of Monodisperse Silica Nanoparticles Dispersable in Non-Polar Solvents,ADVANCED ENGINEERING MATERIALS, Issue 5 2010Eoin Murray Three synthetic routes to hydrophobic silica nanoparticles are compared in this paper. First, the established synthetic method based on the Stöber process was examined. Monodisperse colloidal silica particles with diameters of 15,25,nm were prepared via the hydrolysis of tetraethyl orthosilicate (TEOS) by aqueous ammonia in ethanol. The surfaces of these particles were rendered hydrophobic with octadecyltrimethoxysilane (ODTMS) after the reaction or, more conveniently, during the growth phase. Secondly, silica particles with diameters of 15,50,nm were prepared using a one-pot synthesis in which TEOS was hydrolyzed by an amino acid and the resulting particles were coated with ODTMS. Lastly a novel, direct approach to the synthesis of hydrophobic organosilica nanoparticles was developed using ODTMS as the single silica source. Hydrolysis of the ODTMS by aqueous ammonia in ethanol yielded monodisperse colloidal organosilica particles with diameters of 15,30,nm. [source] A New Series of Quadrupolar Type Two-Photon Absorption Chromophores Bearing 11, 12-Dibutoxydibenzo[a,c]-phenazine Bridged Amines; Their Applications in Two-Photon Fluorescence Imaging and Two-Photon Photodynamic TherapyADVANCED FUNCTIONAL MATERIALS, Issue 15 2009Marappan Velusamy Abstract A new series of quadrupolar type two-photon absorption (2PA) chromophores 3,9 bearing a core arylamine-[a,c]phenazine-arylamine motif are synthesized in high yields. Palladium-catalyzed Stille coupling and CN coupling reactions are utilized to prepare target chromophores. Detailed characterization and systematic studies of these molecules, including absorption and fluorescence emission, are conducted. These compounds are found to exhibit very large 2PA cross section values, for example, ,7000 GM at 800,nm for 8 in toluene. Two-photon-induced fluorescence imaging is successfully demonstrated in vitro using compound- 8 -encapsulated silica nanoparticles with excellent bio-compatibility. In combination with the capability of both one- and two-photon singlet-oxygen sensitizations, this nanocomposite demonstrates its promising potential in dual functionality toward two-photon fluorescence imaging and two-photon photodynamic therapy. [source] Near-Infrared Mesoporous Silica Nanoparticles for Optical Imaging: Characterization and In Vivo BiodistributionADVANCED FUNCTIONAL MATERIALS, Issue 2 2009Chia-Hung Lee Abstract The characterization of near-infrared (NIR) mesoporous silica nanoparticles (MSN) suitable for in vivo optical imaging with high efficiency is presented. Trimethylammonium groups modified MSN (MSN-TA) with the average size of 50,100,nm was synthesized with incorporation of the TA groups into the framework of MSN. It was further adsorbed with indocyanine green (ICG) by electrostatic attraction to render MSN-TA-ICG as an efficient NIR contrast agent for in vivo optical imaging. The studies in stability of MSN-TA-ICG against pH indicated the bonding is stable over the range from acidic to physiological pH. The in vivo biodistribution of MSN-TA-ICG in anesthetized rat demonstrated a rather strong and stable fluorescence of MSN-TA-ICG that prominent in the organ of liver. Transmission electron microscopy (TEM) imaging and elemental analysis of silicon further manifested the physical and quantitative residences of MSN-TA-ICG in major organs. This is the first report of MSN functionalized with NIR-ICG capable of optical imaging in vivo. [source] Designed Fabrication of Silica-Based Nanostructured Particle Systems for Nanomedicine Applications,ADVANCED FUNCTIONAL MATERIALS, Issue 23 2008Yuanzhe Piao Abstract Suitably integrating multiple nanomaterials into nanostructured particle systems with specific combinations of properties has recently attracted significant attention in the research community. In particular, numerous particle systems have been designed and fabricated by integrating diverse materials with monodispersed silica nanoparticles. One or more distinct nanomaterials can be assembled on, encapsulated within, or integrated both inside and on the surface of silica nanoparticles using different chemistries and techniques to create multifunctional nanosystems. Research on these particle systems for biomedical applications has progressed rapidly during recent years due to the synergistic advantages of these complexes compared to the use of single components. This feature article surveys recent research progress on the fabrication strategies of these nanoparticle systems and their applications to medical diagnostics and therapy, thereby paving the way for the emerging field of nanomedicine. [source] Acrylic Nanocomposite Resins for Use in Stereolithography and Structural Light Modulation Based Rapid Prototyping and Rapid Manufacturing Technologies,ADVANCED FUNCTIONAL MATERIALS, Issue 16 2008Matthias Gurr Abstract A novel family of optically transparent acrylic nanocomposites containing up to 30,wt,% silica nanoparticles with an average diameter of 20,nm was developed for application in structural light modulation (SLM) and stereolithography (SL) technologies. The uniform dispersion of nanoparticles affords a significantly improved toughness/stiffness-balance of the photopolymerized and postcured nanocomposites. It is possible to increase stiffness, as expressed by Young's modulus, from 1290 to 1700,MPa without encountering the embrittlement typical for many other conventional filled polymers. Fracture behaviour is examined by means of fracture mechanics investigation and SEM analyses of fracture surfaces. According to TEM analyses and measurement of optical transmittance remarkable uniform dispersion of silica nanoparticles was achieved. The silica nanoparticle concentrations up to 17,wt,% give only marginally higher viscosities and do not affect transmittance, while slightly increasing the exposure times needed in photopolymerization. Moreover, the silica nanoparticles afford materials with reduced shrinkage and improved properties. The green effective ankle splay out (EASO) measured on H-shaped diagnostic specimens, is significantly reduced for the nanocomposite materials from 1.38,mm for the unfilled material to 0.82,mm for nanocomposites containing 30,wt,% nanosilica. The building accuracy is increased significantly with increasing content of silica nanofillers. [source] Layer-By-Layer Assembly of ,-Estradiol Loaded Mesoporous Silica Nanoparticles on Titanium Substrates and Its Implication for Bone HomeostasisADVANCED MATERIALS, Issue 37 2010Yan Hu Drug-loadingmesoporous silica nanoparticles that serve as a nanoreservoir-type drug-delivery system are successfully attached to titanium substrates via the layer-by-layer assembly technique (see scheme). The obtained structure demonstrates great potential for regulating the biological behaviors of osteoblasts/ steoclasts in order to maintain bone homeostasis. The approach we present here may have wide applications in implant technology, tissue engineering, and regenerative medicine. [source] SiO2 Nanoparticle Sequestration via Reactive Functionalization in Holographic Polymer-Dispersed Liquid CrystalsADVANCED MATERIALS, Issue 36 2009John D. Busbee Holographic photopolymerization of reactively functionalized silica nanoparticles in polymer/liquid-crystal systems leads to sequestration of the silica nanoparticles in the polymeric domain of holographic polymer-dispersed liquid-crystals Bragg gratings. Excellent dispersion of the nanoparticles maintains the optical properties of the reflection grating without additional scattering while lowering the voltage necessary to switch the state of the grating. [source] Orthogonal Transformations on Solid Substrates: Efficient Avenues to Surface ModificationADVANCED MATERIALS, Issue 34 2009Leena Nebhani Abstract The performance of solid substrates is not only governed by their molecular constitution, but is also critically influenced by their surface constitution at the solid/gas or solid/liquid interface. In here, we critically review the use of orthogonal chemical transformations (so-called click chemistry) to achieve efficient surface modifications of materials ranging from gold and silica nanoparticles, polymeric films, and microspheres to fullerenes as well as carbon nanotubes. In addition, the functionalization of surfaces via click chemistry with biomolecules is explored. Although a large host of reactions fulfilling the click -criteria exist, pericyclic reactions are most frequently employed for efficient surface modifications. The advent of the click chemistry concept has led,as evident from the current literature,to a paradigm shift in current approaches for materials modification: Away from unspecific and nonselective reactions to highly specific true surface engineering. [source] Nanocomposite Foams: Conducting Nanocomposite Polymer Foams from Ice-Crystal-Templated Assembly of Mixtures of Colloids (Adv. Mater.ADVANCED MATERIALS, Issue 28 200928/2009) The cover shows an electron microscopy image of a nanocomposite "soft" polymer foam reinforced with armored cell walls of "hard" nanoparticles obtained by freeze-drying a mixture of colloids dispersed in water. On p. 2894 Stefan Bon and co-workers demonstrate the versatility of their ice-crystal templating assembly strategy by fabricating a gas sensor from a "soft" polymer latex, silica nanoparticles, and colloidal carbon black. [source] Antimicrobial Activity of Silver Nanocrystals Encapsulated in Mesoporous Silica NanoparticlesADVANCED MATERIALS, Issue 17 2009Monty Liong Silver nanocrystals encapsulated in mesoporous silica nanoparticles are prepared by coating hydrophobic silver nanocrystals with amphiphilic surfactants and growing mesostructured silica around the materials. The nanoparticles can be used as antimicrobial agents for both Gram-positive and -negative bacteria through oxidative dissolution of the silver nanocrystals. The surface characteristics of the silica exterior affect the binding to the bacteria and the cytotoxicity. [source] In vitro Studies of Functionalized Mesoporous Silica Nanoparticles for Photodynamic TherapyADVANCED MATERIALS, Issue 2 2009Hsiung-Lin Tu A versatile platform for photodynamic therapy (PDT), mesoporous silica nanoparticles functionalized with protoporphyrin IX (PpIX-MSNs), has been developed. In vitro studies on HeLa cells show high uptake efficiency. Phototoxicity results give both irradiation time- and dosage-dependent cell death events. Because of the ease of incorporating other biomedical functional groups, we believe MSNs would be an ideal platform for biomedical applications. [source] Nanoscale Engineering of Biomaterial Surfaces,ADVANCED MATERIALS, Issue 4 2007M. Lipski Single-step independent modification of the texture and chemistry of a material surface through the assembly of functionalized silica nanoparticles (NPs) is described. Such NP surface modifications enhance the differentiation of human-marrow-derived mesenchymal cells into an osteogenic lineage and present a new paradigm for nanoscale biomimetic engineering of a biomaterial surface. [source] Hybrid Inorganic-Organic Materials Carrying Tertiary Amine and Thiourea Residues Tethered on Mesoporous Silica Nanoparticles: Synthesis, Characterization, and Co-Operative CatalysisADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 1-2 2009Alessandra Puglisi Abstract Mesoporous silica nanoparticles carrying different loadings of tertiary amine and thiourea residues (residues ratios 53/47, 68/32, and 22/78, respectively) were synthesized by the co-condensation method and fully characterized by CP MAS NMR, powder XRD, SEM, BET, BJH and FT-IR techniques. These materials were tested as bifunctional catalysts in the conjugate addition of acetylacetone to 2-nitrostyrene, a reaction that under solvent-free conditions occurred in quantitative yield. By carrying out several experiments with the bifunctional catalysts featuring different molar ratios of active sites, and with different combinations of monofunctional supported and non-supported catalyst, the co-operativity of the tertiary amine and thiourea residues in catalyzing the reaction was demonstrated. The use of the bifunctional catalyst was extended to the addition of acetylacetone to an activated imine. Catalyst recycling for a total of three reaction cycles was demonstrated without significant erosion of activity. [source] Epoxy composites reinforced by different size silica nanoparticlesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2010Cheng-Fang Ou Abstract Three series of epoxy/SiO2 composites, containing 0.3,7 wt % nanosized SiO2 with different specific surface area, were prepared by solution blending. The resulting composites exhibit the higher glass transition temperature (Tg) than that of pure epoxy. The Tg of composite showed a maximum increment of 35.3°C by the addition of 7 wt % A300. The trade name of A300 is Aerosil 300. It is one of the fumed silica nanoparticles products of Degussa. The decomposition temperatures (Td) of composites were always higher than that of pure epoxy and showed a maximum increment of 20.8°C by the addition of 5 wt % A300. The light transmittance of composites was as a function of the SiO2 content and size. The water permeability of composites decreased with increasing SiO2 content and the 7 wt % A300 composite exhibits a maximum decrement percentage of 35.6%. The Tg, Td, storage modulus, and water-vapor barrier property are as a function of the SiO2 content and size. These properties increased as the content of SiO2 increased. The finer SiO2 are more effective in increasing the Tg, Td, and water-vapor barrier property. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Effect of the structure of silane-coupling agent on dynamic mechanical properties of dental resin-nanocompositesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2008Irini D. Sideridou Abstract This work was aimed at the study by dynamic mechanical analysis (DMA) of dental composites consisted of a Bis-GMA/TEGDMA (50/50 wt/wt) matrix and silica nanoparticles (Aerosil OX50) as filler, silanized with various silanes. The silanes used were 3-[(1,3(2)-dimethacryloyloxypropyl)-2 (3)-oxycarbonylamido] propyltriethoxy-silane (UDMS), 3-methacryloxypropyl-trimethoxysilane (MPS), octyltrimethoxysilane (OTMS), blends of UDMS/OTMS (50/50 wt/wt), or MPS/OTMS (50/50 wt/wt). The total amount of silane was kept constant at 10% by weight fraction relative to the filler weight. The silanized nanoparticles were mixed with the dimethacrylate matrix (60% filler by weight fraction). The composites were light cured and tested by DMA for the determination of storage modulus (E,), loss modulus (E,), tangent delta (tan ,), and glass transition temperature (Tg). Measurements were performed in samples immediately after curing and samples stored in water at 37°C for 1, 7, 30, or 120 days. OTMS-composite in which OTMS does not form covalent bond with the dimethacrylate matrix showed lower elastic modulus both in dry and wet conditions. The ability of bifunctional UDMS for crosslinking was found not to increase the elastic behavior of the composite, as it was expected, compared with that of MPS-composite, because of the high amount of the silane used. After immersion in water the elastic modulus of OTMS-composite remained constant, while that of the other composites increased after 1 day and then remained constant up to 120 days. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [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] Mechanochemical modification of silica with poly(1-vinyl-2-pyrrolidone) by grinding in a stirred media millJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2007Voronov A. Abstract The polymerization of 1-vinyl-2-pyrrolidone (VP) mechanochemically initiated by grinding silica was investigated in a wet stirred media mill. The polymerization itself proceeds from the silica grinding without any additional initiator. We have found that the amount of grafted polymer increases with an increase in total ground silica surface. The suspension of polymer-modified silica nanoparticles showed high colloidal stability in water because of the appearance of grafted hydrophilic PVP on the surface during the reactive grinding. Because the nanoparticles SiO2 - graft -PVP are biocompatible, the developed polymer nanocomposite material can be of particular interest for the performance of membranes and for the fabrication of biocompatible hydrogels with enhanced mechanical properties and porosity. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 3708,3714, 2007 [source] Pyrolysis studies of polyethylene terephthalate/silica nanocompositesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2007Jin Zheng Abstract The decomposition of pure polyethylene terephthalate (PET) and PET/silica nanocomposites was investigated by thermal gravimetry (TG) and pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS). The influence of the nanosized silica on the pyrolysis properties of the composites was found from the results that the activation energies of decomposition and the residual carbon content increase with silica nanoparticles. It is deduced that the increase of the activation energies and the residual carbon content result from the adsorption of the decomposed products on the surface of silica. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 2007 [source] | ||||||||||||||||||||||||||||||||||