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Siloxane
Kinds of Siloxane Terms modified by Siloxane Selected AbstractsFormation and Properties of Responsive Siloxane-Based Polymeric Surfaces with Tunable Surface Reconstruction KineticsADVANCED FUNCTIONAL MATERIALS, Issue 3 2009Julie Ann Crowe-Willoughby Abstract Here, the formation of responsive polymeric materials with tunable response time is reported. These structures are fabricated by chemically modifying poly(vinylmethyl siloxane) (PVMS) networks with alkanethiols bearing a hydrophilic end-group (COOH or OH). The response time is facilitated by the liquid nature of the PVMS backbone and increases with increase in length of the methylene spacer (CH2)n in the alkanethiol pendent group. While for n,=,2 and 6, the surface reconstructs almost instantaneously, specimens with n,=,11 resist reconstruction because of strong van der Waals forces, leading to the formation of semi-crystalline regions. It is demonstrated that the responsive nature of PVMSS(CH2)11OH can be fine-tuned by varying the temperature; it possesses a faster response at temperatures above the melting point of the S(CH2)11OH moiety. [source] Multiple Applications of Polyvinyl SiloxaneJOURNAL OF PROSTHODONTICS, Issue 3 2000Johvin Perry DDS [source] Numerical simulation of dense gas flows on unstructured grids with an implicit high resolution upwind Euler solverINTERNATIONAL JOURNAL FOR NUMERICAL METHODS IN FLUIDS, Issue 7 2004P. Colonna Abstract The study of the dense gas flows which occur in many technological applications demands for fluid dynamic simulation tools incorporating complex thermodynamic models that are not usually available in commercial software. Moreover, the software mentioned can be used to study very interesting phenomena that usually go under the name of ,non-classical gasdynamics', which are theoretically predicted for high molecular weight fluids in the superheated region, close to saturation. This paper presents the numerical methods and models implemented in a computer code named zFlow which is capable of simulating inviscid dense gas flows in complex geometries. A detailed description of the space discretization method used to approximate the Euler equations on unstructured grids and for general equations of state, and a summary of the thermodynamic functions required by the mentioned formulation are also given. The performance of the code is demonstrated by presenting two applications, the calculation of the transonic flow around an airfoil computed with both the ideal gas and a complex equation of state and the simulation of the non-classical phenomena occurring in a supersonic flow between two staggered sinusoidal blades. Non-classical effects are simulated in a supersonic flow of a siloxane using a Peng,Robinson-type equation of state. Siloxanes are a class of substances used as working fluids in organic Rankine cycles turbines. Copyright © 2004 John Wiley & Sons, Ltd. [source] ChemInform Abstract: New in situ Generated Ruthenium Catalyst for Enyne Metathesis: Access to Novel Cyclic Siloxanes.CHEMINFORM, Issue 24 2001David Semeril 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] Mechanical and morphological properties of organic,inorganic, hybrid, clay-filled, and cyanate ester/siloxane toughened epoxy nanocompositesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2007S. Nagendiran Abstract Organic,inorganic hybrids involving cyanate ester and hydroxyl-terminated polydimethylsiloxane (HTPDMS) modified diglycidyl ether of bisphenol A (DGEBA; epoxy resin) filled with organomodified clay [montmorillonite (MMT)] nanocomposites were prepared via in situ polymerization and compared with unfilled-clay macrocomposites. The epoxy-organomodified MMT clay nanocomposites were prepared by the homogeneous dispersion of various percentages (1,5%), and the resulting homogeneous epoxy/clay hybrids were modified with 10% HTPDMS and ,-aminopropyltriethoxysilane as a coupling agent in the presence of a tin catalyst. The siliconized epoxy/clay prepolymer was further modified separately with 10% of three different types of cyanate esters, namely, 4,4,-dicyanato-2,2,-diphenylpropane, 1,1,-bis(3-methyl-4-cyanatophenyl) cyclohexane, and 1,3-dicyanato benzene, and cured with diaminodiphenylmethane as a curing agent. The reactions during the curing process between the epoxy, siloxane, and cyanate were confirmed by Fourier transform infrared analysis. The results of dynamic mechanical analysis showed that the glass-transition temperatures of the clay-filled hybrid epoxy systems were lower than that of neat epoxy. The data obtained from mechanical studies implied that there was a significant improvement in the strength and modulus by the nanoscale reinforcement of organomodified MMT clay with the matrix resin. The morphologies of the siloxane-containing, hybrid epoxy/clay systems showed heterogeneous character due to the partial incompatibility of HTPDMS. The exfoliation of the organoclay was ascertained from X-ray diffraction patterns. The increase in the percentage of organomodified MMT clay up to 5 wt % led to a significant improvement in the mechanical properties and an insignificant decrease in the glass-transition temperature versus the unfilled-clay systems. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 [source] Recent progress in the development, characterization and application of polymeric pseudophases for electrokinetic chromatographyELECTROPHORESIS, Issue 22-23 2002Christopher P. Palmer Abstract This review article details the development, characterization and application of polymeric materials as pseudostationary phases for electrokinetic chromatography over the past two years. Recent developments in cationic polymers and anionic siloxane, acrylamide and polymerized surfactants (micelle polymers) are reviewed. Also reviewed is recent progress in the development and characterization of chiral polymeric phases for chiral separations by electrokinetic chromatography, and application of a polymeric pseudophase with electrospray ionization mass spectrometric detection. [source] Functionalized-Silk-Based Active Optofluidic DevicesADVANCED FUNCTIONAL MATERIALS, Issue 7 2010Konstantinos Tsioris Abstract Silk protein from the silkworm Bombyx mori has excellent chemical and mechanical stability, biocompatibility, and optical properties. Additionally, when the protein is purified and reformed into materials, the biochemical functions of dopants entrained in the protein matrix are stabilized and retained. This unique combination of properties make silk a useful multifunctional material platform for the development of sensor devices. An approach to increase the functions of silk-based devices through chemical modifications to demonstrate an active optofluidic device to sense pH is presented. Silk protein is chemically modified with 4-aminobenzoic acid to add spectral-color-responsive pH sensitivity. The functionalized silk is combined with the elastomer poly(dimethyl siloxane) in a single microfluidic device. The microfluidic device allows spatial and temporal control of the delivery of analytic solutions to the system to provide the optical response of the optofluidic device. The modified silk is stable and spectrally responsive over a wide pH range from alkaline to acidic. [source] Formation and Properties of Responsive Siloxane-Based Polymeric Surfaces with Tunable Surface Reconstruction KineticsADVANCED FUNCTIONAL MATERIALS, Issue 3 2009Julie Ann Crowe-Willoughby Abstract Here, the formation of responsive polymeric materials with tunable response time is reported. These structures are fabricated by chemically modifying poly(vinylmethyl siloxane) (PVMS) networks with alkanethiols bearing a hydrophilic end-group (COOH or OH). The response time is facilitated by the liquid nature of the PVMS backbone and increases with increase in length of the methylene spacer (CH2)n in the alkanethiol pendent group. While for n,=,2 and 6, the surface reconstructs almost instantaneously, specimens with n,=,11 resist reconstruction because of strong van der Waals forces, leading to the formation of semi-crystalline regions. It is demonstrated that the responsive nature of PVMSS(CH2)11OH can be fine-tuned by varying the temperature; it possesses a faster response at temperatures above the melting point of the S(CH2)11OH moiety. [source] Preparation of Functional Hybrid Glass Material from Platinum (II) Complexes for Broadband Nonlinear Absorption of LightADVANCED FUNCTIONAL MATERIALS, Issue 2 2009Roman Zieba Abstract The synthesis of trans -di(arylalkynyl)diphosphine platinum(II) complexes bearing trialkoxysilane groups is described, as well as the preparation of siloxane-based hybrid materials from organometallic chromophores through a modified sol,gel process. Glass materials prepared from trans -[P(n,Bu)3]2Pt[(C,C,p,C6H4,C,C,p,C6H4,CH2O(CO)NH(CH2)3Si(OC2H5)3]2 generally show spectral transmittance, absorption and luminescence similar to that of solutions reported in the literature. Measurements of optical power limiting for the hybrid glass are carried out, and show broadband nonlinear absorption throughout the whole visible wavelength range with clamping values in the range 0.2,7,µJ at 120,mM chromophore concentration. The sol,gel process using urethane-propyltriethoxysilane-functionalized chromophores as precursors appears to be a valid method for formation of robust silicate materials with grafted diarylethynyl Pt(II) complexes for OPL devices. [source] Lanthanide-Containing Light-Emitting Organic,Inorganic Hybrids: A Bet on the FutureADVANCED MATERIALS, Issue 5 2009Luís D. Carlos Abstract Interest in lanthanide-containing organic,inorganic hybrids has grown considerably during the last decade, with the concomitant fabrication of materials with tunable attributes offering modulated properties. The potential of these materials relies on exploiting the synergy between the intrinsic characteristics of sol,gel derived hosts (highly controlled purity, versatile shaping and patterning, excellent optical quality, easy control of the refractive index, photosensitivity, encapsulation of large amounts of isolated emitting centers protected by the host) and the luminescence features of trivalent lanthanide ions (high luminescence quantum yield, narrow bandwidth, long-lived emission, large Stokes shifts, ligand-dependent luminescence sensitization). Promising applications may be envisaged, such as light-emitting devices, active waveguides in the visible and near-IR spectral regions, active coatings, and bio-medical actuators and sensors, opening up exciting directions in materials science and related technologies with significant implications in the integration, miniaturization, and multifunctionalization of devices. This review provides an overview of the latest advances in Ln3+ -containing siloxane-based hybrids, with emphasis on the different possible synthetic strategies, photoluminescence features, empirical determination [source] Numerical simulation of dense gas flows on unstructured grids with an implicit high resolution upwind Euler solverINTERNATIONAL JOURNAL FOR NUMERICAL METHODS IN FLUIDS, Issue 7 2004P. Colonna Abstract The study of the dense gas flows which occur in many technological applications demands for fluid dynamic simulation tools incorporating complex thermodynamic models that are not usually available in commercial software. Moreover, the software mentioned can be used to study very interesting phenomena that usually go under the name of ,non-classical gasdynamics', which are theoretically predicted for high molecular weight fluids in the superheated region, close to saturation. This paper presents the numerical methods and models implemented in a computer code named zFlow which is capable of simulating inviscid dense gas flows in complex geometries. A detailed description of the space discretization method used to approximate the Euler equations on unstructured grids and for general equations of state, and a summary of the thermodynamic functions required by the mentioned formulation are also given. The performance of the code is demonstrated by presenting two applications, the calculation of the transonic flow around an airfoil computed with both the ideal gas and a complex equation of state and the simulation of the non-classical phenomena occurring in a supersonic flow between two staggered sinusoidal blades. Non-classical effects are simulated in a supersonic flow of a siloxane using a Peng,Robinson-type equation of state. Siloxanes are a class of substances used as working fluids in organic Rankine cycles turbines. Copyright © 2004 John Wiley & Sons, Ltd. [source] Synthesis, characterization, and comparison of properties of novel fluorinated poly(imide siloxane) copolymersJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2008Anindita Ghosh Abstract Four new poly(imide siloxane) copolymers were prepared by a one-pot solution imidization method at a reaction temperature of 180°C in ortho -dichlorobenzene as a solvent. The polymers were made through the reaction of o -diphthaleic anhydride with four different diamines,4,4,-bis(p -aminophenoxy-3,3,-trifluoromethyl) terphenyl, 4,4,-bis(3,-trifluoromethyl- p -aminobiphenyl ether)biphenyl, 2,6-bis(3,-trifluoromethyl- p -aminobiphenyl ether)pyridine, and 2,5-bis(3,-trifluoromethyl- p -aminobiphenylether)thiopene,and aminopropyl-terminated poly dimethylsiloxane as a comonomer. The polymers were named 1a, 1b, 1c, and 1d, respectively. The synthesized polymers showed good solubility in different organic solvents. The resulting polymers were well characterized with gel permeation chromatography, IR, and NMR techniques. 1H-NMR indicated that the siloxane loading was about 36%, although 40 wt % was attempted. 29Si-NMR confirmed that the low siloxane incorporation was due to a disproportionation reaction of the siloxane chain that resulted in a lowering of the siloxane block length. The films of these polymers showed low water absorption of 0.02% and a low dielectric constant of 2.38 at 1 MHz. These polyimides showed good thermal stability with decomposition temperatures (5% weight loss) up to 460°C in nitrogen. Transparent, thin films of these poly(imide siloxane)s exhibited tensile strengths up to 30 MPa and elongations at break up to 103%, which depended on the structure of the repeating unit. The rheological properties showed ease of processability for these polymers with no change in the melt viscosity with the temperature. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Mechanical and morphological properties of organic,inorganic, hybrid, clay-filled, and cyanate ester/siloxane toughened epoxy nanocompositesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2007S. Nagendiran Abstract Organic,inorganic hybrids involving cyanate ester and hydroxyl-terminated polydimethylsiloxane (HTPDMS) modified diglycidyl ether of bisphenol A (DGEBA; epoxy resin) filled with organomodified clay [montmorillonite (MMT)] nanocomposites were prepared via in situ polymerization and compared with unfilled-clay macrocomposites. The epoxy-organomodified MMT clay nanocomposites were prepared by the homogeneous dispersion of various percentages (1,5%), and the resulting homogeneous epoxy/clay hybrids were modified with 10% HTPDMS and ,-aminopropyltriethoxysilane as a coupling agent in the presence of a tin catalyst. The siliconized epoxy/clay prepolymer was further modified separately with 10% of three different types of cyanate esters, namely, 4,4,-dicyanato-2,2,-diphenylpropane, 1,1,-bis(3-methyl-4-cyanatophenyl) cyclohexane, and 1,3-dicyanato benzene, and cured with diaminodiphenylmethane as a curing agent. The reactions during the curing process between the epoxy, siloxane, and cyanate were confirmed by Fourier transform infrared analysis. The results of dynamic mechanical analysis showed that the glass-transition temperatures of the clay-filled hybrid epoxy systems were lower than that of neat epoxy. The data obtained from mechanical studies implied that there was a significant improvement in the strength and modulus by the nanoscale reinforcement of organomodified MMT clay with the matrix resin. The morphologies of the siloxane-containing, hybrid epoxy/clay systems showed heterogeneous character due to the partial incompatibility of HTPDMS. The exfoliation of the organoclay was ascertained from X-ray diffraction patterns. The increase in the percentage of organomodified MMT clay up to 5 wt % led to a significant improvement in the mechanical properties and an insignificant decrease in the glass-transition temperature versus the unfilled-clay systems. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 [source] Equivalences between refractive index and equilibrium water content of conventional and silicone hydrogel soft contact lenses from automated and manual refractometry,JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 1 2007José M. González-Méijome Abstract Purpose The purpose of the present study was to develop mathematical relationships that allow obtaining equilibrium water content and refractive index of conventional and silicone hydrogel soft contact lenses from refractive index measures obtained with automated refractometry or equilibrium water content measures derived from manual refractometry, respectively. Methods Twelve HEMA-based hydrogels of different hydration and four siloxane-based polymers were assayed. A manual refractometer and a digital refractometer were used. Polynomial models obtained from the sucrose curves of equilibrium water content against refractive index and vice-versa were used either considering the whole range of sucrose concentrations (16,100% equilibrium water content) or a range confined to the equilibrium water content of current soft contact lenses (,20,80% equilibrium water content). Results Values of equilibrium water content measured with the Atago N-2E and those derived from the refractive index measurement with CLR 12,70 by the applications of sucrose-based models displayed a strong linear correlation (r2 = 0.978). The same correlations were obtained when the models are applied to obtain refractive index values from the Atago N-2E and compared with those (values) given by the CLR 12,70 (r2 = 0.978). No significantly different results are obtained between models derived from the whole range of the sucrose solution or the model limited to the normal range of soft contact lens hydration. Conclusions Present results will have implications for future experimental and clinical research regarding normal hydration and dehydration experiments with hydrogel polymers, and particularly in the field of contact lenses. © 2006 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2007 [source] VISCOELASTICITY OF A SIMULATED POLYMER AND COMPARISON WITH CHICKPEA FLOUR DOUGHSJOURNAL OF FOOD PROCESS ENGINEERING, Issue 3 2006NIDHI YADAV ABSTRACT An integrated approach consisting of compression and stress relaxation is performed with a simulated model system of poly dimethyl siloxane (PDMS), a viscoelastic polymer material when the compressive strain, height of sample and crosshead speed were varied. The parameters derived are the forces at the end of compression and relaxation, energy for compression and the extent of elasticity of the sample based on the ratios of forces as well as the proposed energy values. The results were verified with food doughs undergoing large deformations that show a nonlinear behavior. The proposed extent of elasticity based on the ratios of energy stored and compression can be used as an index for the characterization of viscoelasticity. A nonlinear three-parameter model had also been proposed to predict the stress decay characteristics as a function of time, which was found suitable for the PDMS system, and was better than the two-parameter Peleg model as judged by lower variance values (0.0006,0.018 and 0.002,0.048, respectively). Further, an actual system of food doughs in the form of chickpea (Cicer arietinum L.) flour dough was used to verify the proposed model and viscoelastic index at different moisture contents (27,39%) subjected to compressive strains of 25,75%. The nonlinear relaxation characteristics of the food dough are sensitive to moisture content as well as to strain level. [source] Effect of surface modifying macromolecules stoichiometric ratio on composite hydrophobic/hydrophilic membranes characteristics and performance in direct contact membrane distillationAICHE JOURNAL, Issue 12 2009M. Qtaishat Abstract The stoichiometric ratio for the synthesis components of hydrophobic new surface modifying macromolecules (nSMM) was altered systematically to produce three different types of nSMMs, which are called hereafter nSMM1, nSMM2, and nSMM3. The newly synthesized SMMs were characterized for fluorine content, average molecular weight, and glass transition temperature. The results showed that fluorine content decreased with increasing the ratio of ,,,-aminopropyl poly(dimethyl siloxane) to 4,4,-methylene bis(phenyl isocyanate). The synthesized nSMMs were blended into hydrophilic polyetherimide (PEI) host polymer to form porous hydrophobic/hydrophilic composite membranes by the phase inversion method. The prepared membranes were characterized by the contact angle measurement, X-ray photoelectron spectroscopy, gas permeation test, measurement of liquid entry pressure of water, and scanning electron microscopy. Finally, these membranes were tested for desalination by direct contact membrane distillation and the results were compared with those of commercial polytetraflouroethylene membrane. The effects of the nSMM type on the membrane morphology were identified, which enabled us to link the membrane morphology to the membrane performance. It was found that the nSMM2/PEI membrane yielded the best performance among the tested membranes. In particular, it should be emphasized that the above membrane was superior to the commercial one. © 2009 American Institute of Chemical Engineers AIChE J, 2009 [source] Synthesis and characterization of fluorene-based copolymers containing siloxane or distilbene moieties on their main chainJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 6 2009Hoon-Je Cho Abstract Two novel types of polyfluorene copolymers containing siloxane linkages or distilbene moieties on their main-chains were synthesized by Ni(0)-mediated Yamamoto coupling polymerization. These polymers, designated P2Silo05, P2Silo15, PF-P02, and PF-P05 were prepared by copolymerization between 2,7-dibromo-9,9,-dihexylfluorene and bis(bromobenzene)-terminated disiloxane monomer (for P2Silo05 and P2Silo15) or dibromodistilbene monomer (for PF-P02 and PF-P05). All of the polymers were highly soluble in common organic solvents such as chloroform, toluene, and p -xylene. The glass transition temperatures of the polymers were between 92 and 113 °C, and the decomposition temperatures for a 5% weight loss (Td) were above 420 °C for all of the polymers, demonstrating high thermal stability. The molecular weight (Mw) of the polymers ranged from 4.2 × 104 to 8.8 × 104. The blue shift of the maximum in the UV-visible absorption was greater in polymers with a higher molar percentage of siloxane linkages or distilbene moieties than in homo poly (dihexylfluorene) (PDHF). However, the photoluminescence spectra of the polymers were similar to those of PDHF in terms of the onsets and patterns. Single-layer light-emitting diodes were fabricated with a configuration of ITO/PEDOT:PSS/polymers/Ca/Al. The maximum electroluminescence emission wavelengths of the polymers were 425,450 nm, corresponding to pure blue light. The CIE co-ordinates of the polyfluorenes containing siloxane linkages or distilbene moieties ranged from (0.21, 0.21) to (0.17, 0.10), indicating deeper blue light than that of PDHF {CIE co-ordinates of (0.25, 0.29)}, with P2Silo15 giving the deepest blue-light {CIE co-ordinates of (0.17, 0.10)}. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 1595,1608, 2009 [source] Synthesis and characterization of poly[styrene- b -methyl(3,3,3-trifluoropropyl)siloxane] diblock copolymers via anionic polymerizationJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 19 2005Lingmin Yi Abstract A series of narrow molecular weight distribution (MWD) polystyrene- b -poly[methyl(3,3,3-trifluoropropyl)siloxane] (PS- b -PMTFPS) diblock copolymers were synthesized by the sequential anionic polymerization of styrene and trans -1,3,5-trimethyl-1,3,5-tris(3,,3,,3,-trifluoropropyl)cyclotrisiloxane in tetrahydrofuran (THF) with n -butyllithium as the initiator. The diblock copolymers had narrow MWDs ranging from 1.06 to 1.20 and number-average molecular weights ranging from 8.2 × 103 to 37.1 × 103. To investigate the properties of the copolymers, diblock copolymers with different weight fractions of poly[methyl(3,3,3-trifluoropropyl)siloxane] (15.4,78.8 wt %) were prepared. The compositions of the diblock copolymers were calculated from the characteristic proton integrals of 1H NMR spectra. For the anionic ring-opening polymerization (ROP) of 1,3,5-trimethyl-1,3,5-tris(3,,3,,3,-trifluoropropyl)cyclotrisiloxane (F3) initiated by polystyryllithium, high monomer concentrations could give high polymer yields and good control of MWDs when THF was used as the polymerization solvent. It was speculated that good control of the block copolymerization under the condition of high monomer concentrations was due to the slowdown of the anionic ROP rate of F3 and the steric hindrance of the polystyrene precursors. There was enough time to terminate the ROP of F3 when the polymer yield was high, and good control of block copolymerization could be achieved thereafter. The thermal properties (differential scanning calorimetry and thermogravimetric analysis) were also investigated for the PS- b -PMTFPS diblock copolymers. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 4431,4438, 2005 [source] Synthesis and second-order nonlinear optical properties of multifunctional polysiloxanes with sulfonyl-based chromophoresJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 7 2005Jianli Hua Abstract Two new polysiloxanes (P1 and P2) with a high density of sulfonyl-based chromophores were prepared by a new two-step method. Poly[methyl-3-(9-carbazolyl)propyl siloxane] was partially formulated by the standard Vilsmeier reaction, and formyl groups of high reactivity were condensed with cyanoacetylated chromophores; this yielded polysiloxanes P1 and P2 in almost complete conversions. Their structures were verified with 1H NMR, IR, and ultraviolet,visible spectra. P1 and P2 exhibited good solubility in common organic solvents and were thermally stable. The maximum absorptions appeared at about 452 and 390 nm for P1 and P2, respectively, in tetrahydrofuran; they were blueshifted about 42 and 8 nm, respectively, in comparison with those of the corresponding chromophores with a nitro acceptor and resulted in a wider transparency window. The P1 values of the nonlinear optical coefficient (d33), measured by in situ second harmonic generation, was 16.2 pm/V. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 1317,1324, 2005 [source] Synthesis and cationic photopolymerization of epoxy-functional siloxane monomers and oligomersJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 19 2003Myoungsouk Jang Abstract A series of difunctional silicon-containing monomers were prepared with a novel method consisting of the monohydrosilation of an ,,,-difunctional SiH-terminated siloxane with a vinyl-functional epoxide or oxetane followed by the dehydrodimerization of the resulting SiH-functional intermediate. This method used simple, readily available starting materials and could be conducted as a streamlined one-pot, two-step synthesis. This novel method was also applied to the synthesis of several epoxy,silicone oligomers. The reactivities of these new monomers and oligomers were examined with Fourier transform real-time infrared spectroscopy and optical pyrometry. Those monomers containing epoxycyclohexyl groups displayed excellent reactivity in cationic ring-opening polymerization in the presence of lipophilic onium salt photoinitiators. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 3056,3073, 2003 [source] Influence of Matrix Type on Surface Roughness of Three Resins for Provisional Crowns and Fixed Partial DenturesJOURNAL OF PROSTHODONTICS, Issue 2 2009Raul Ayuso-Montero DDS Abstract Purpose: This study evaluated the effect of matrix type on the surface roughness of resins for provisional crowns and fixed partial dentures. Materials and Methods: Ninety specimens of two acrylic resins (Trim II, Tab2000) and one bis-acryl composite (Protemp II Garant) were fabricated using one of three matrices: irreversible hydrocolloid (Cavex CA37), poly(vinyl siloxane) (Aquasil) or vacuum-formed matrix (Bio-flow Hard). The sample size for each resin-matrix combination was 10. The vestibular face of one natural maxillary central incisor was used as a model to fabricate all the specimens, following the custom fabrication technique. The average roughness measurements, Ra (,m), were obtained using a profilometer, and the data were analyzed using Kruskal-Wallis and Mann-Whitney U- tests. The results were contrasted against the surface roughness of the tooth using a one-sample t- test. Results: Aquasil and vacuum-formed matrix had a smoother surface than Cavex CA37 regardless of the resin tested (p < 0.05). Protemp II Garant had the smoothest surface regardless of the matrix used, with no significant differences when polymerized against the three different matrices. Trim II polymerized against Cavex CA37 had a rougher (p < 0.05) surface than Aquasil or vacuum-formed matrix. Tab2000 had the smoothest surface (p < 0.05) when polymerized against a vacuum-formed matrix. Conclusions: There is no universal matrix that produces the smoothest surface: this depends on the compatibility between the resin and the matrix. Protemp II Garant polymerized against Cavex CA37 matrix yields a surface that is smooth enough not to require polishing unless this surface is adjusted. [source] Dentist Communication with the Dental Laboratory for Prosthodontic Treatment Using ImplantsJOURNAL OF PROSTHODONTICS, Issue 3 2006Zahra Afsharzand DMD Purpose: A questionnaire was sent to U.S. dental laboratories to evaluate the level of communication between dentists and laboratory technicians and to determine trends in procedures and materials used in fixed and removable implant restorations. Methods and Materials: Dental laboratories were randomly chosen from the National Association of Dental Laboratories for each of the 50 states. The questionnaire was mailed to the laboratory directors for 199 dental laboratories. One hundred fourteen dental laboratories returned the survey, yielding a response rate of 57%. Of those laboratories, 37 indicated that they did not participate in the fabrication of fixed implant restorations, yielding a response rate of 39%. Forty-two dental laboratories indicated that they did not participate in the fabrication of implant-retained overdenture prostheses, yielding a response rate of 36%. Results: Results from this survey show inadequate communication by dentists in completing work authorization forms. Custom trays are used more frequently for implant-retained overdenture impressions and stock trays for impressions of fixed implant prostheses. Poly(vinyl siloxane) is the material most commonly used for both fixed and removable implant-supported prostheses. Two implants with stud attachments are used more widely than those with bar attachments for implant-retained overdentures. Conclusions: Most laboratories working on implant prosthodontic cases report inadequate communication between the laboratory and dentists related to materials and techniques used in fabrication of implant restorations. [source] Structural formation of hybrid siloxane-based polymer monolith in confined spacesJOURNAL OF SEPARATION SCIENCE, JSS, Issue 10-11 2004Kazuyoshi Kanamori Abstract Structural deformation of phase-separated methylsiloxane gel under the influence of a surface has been studied. Competitive wetting of siloxane gel phase on a surface during phase formation is found to significantly affect the final morphology in a confined space. When the spinodal wavelength is sufficiently shorter than the size of the available space, a uniform bicontinuous structure forms in confined geometry. However, gel skeletons in the vicinity of a surface are elongated with decreasing size of the space, and finally when the size of the space becomes shorter than the spinodal wavelength, all the gel phase wets on a surface, showing a "wetting transition". Homogeneous bicontinuous methylsiloxane gels were successfully prepared, avoiding such structural deformation, in a long cylindrical fused silica capillary and used for capillary HPLC. The capillary gels exhibited excellent separation efficiency of nitrobenzenes and it was found that the surface character can be altered by incorporating surfactants, which will enable more advanced and extended control of surface character, depending on the analytes. [source] Fibrinolytic Poly(dimethyl siloxane) SurfacesMACROMOLECULAR BIOSCIENCE, Issue 9 2008Hong Chen Abstract PDMS surfaces have been modified to confer both resistance to non-specific protein adsorption and clot lyzing properties. The properties and chemical compositions of the surfaces have been investigated using water contact angle measurements, ATR FT-IR spectroscopy, and XPS. The ability of the PEG component to suppress non-specific protein adsorption was assessed by measurement of radiolabeled fibrinogen uptake from buffer. The adsorption of plasminogen from human plasma to the various surfaces was studied. In vitro experiments demonstrated that lysine-immobilized surfaces with free , -amino groups were able to dissolve fibrin clots, following exposure to plasma and tissue plasminogen activator. [source] Fabrication of Artificial Petal Sculptures by Replication of Sub-micron Surface Wrinkles,MACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 2 2010Alexandra Schweikart Abstract In this contribution, we discuss wrinkling as a process resulting in well-defined periodic micron-sized structures, as known from the interface of several plant cells. We show possible pathways to transfer this principle to artificial materials such as epoxy resins or polymers. While topographical structuring of surfaces by wrinkling is meanwhile well established for elastomers like poly (dimethyl siloxane), so far the step towards other classes of materials has not been taken. This puts several limitations to potential applications of artificial wrinkled structures, as elastomers show poor dimensional stability, low optical quality, and tend to swell in organic solvents. As well, artificial structures formed by wrinkling are not tension-free on the microscopic level, which makes them metastable. Residual mechanical tensions can affect dimensional stability on long timescales. We introduce two processes, micro thermoforming and molding, as means to overcome these restrictions and to pattern non-elastomeric materials by using wrinkled elastomers as templates. The two approaches allow the formation of negative and positive replicas and allow the transfer of sub-micron features with high fidelity. [source] Influence of Particle Morphology and Flow Conditions on the Dispersion Behavior of Fumed Silica in Silicone PolymersPARTICLE & PARTICLE SYSTEMS CHARACTERIZATION, Issue 3 2004John Boyle Abstract The dispersion behavior of agglomerates of several grades of fumed silica in poly(dimethyl siloxane) liquids has been studied as a function of particle morphology and applied flow conditions. The effects of primary particle size and aggregate density and structure on cohesivity were probed through tensile and shear strength tests on particle compacts. These cohesivity tests indicated that the shear strength of particle compacts was two orders of magnitude higher than the tensile strength at the same overall packing density. Experiments carried out in both steady and time-varying simple-shear flows indicate that dispersion occurs through tensile failure. In the steady-shear experiments,enhanced dispersion was obtained at higher levels of applied stress and, at comparable levels of applied stress, dispersion was found to proceed faster at higher shear rates. Experiments conducted in time-varying flows further corroborated the results obtained in tensile cohesivity tests. Experiments in which the mean and maximum stresses in the time-varying flows were matched to the stresses produced in steady shear flows highlight the influence of flow dynamics on dispersion behavior. [source] Epoxy nanocomposites curing by microwavesPOLYMER ENGINEERING & SCIENCE, Issue 8 2006Nurseli Uyan In this work, chemically modified sodium montmorillonite and epoxy monomer were used to prepare nanocomposites in two consecutive stages. In the first stage, dodecylamine, octadecylamine, hexadecylamine, and hexadecyltrimethyl ammonium bromide were used to prepare various organophilic clays. In the second stage, the bisphenol-A based epoxy monomer and predetermined amounts of organoclay were mixed together and then cured by an aliphatic polyamine for 20 min under microwave at 400 W. Furthermore, ,-, diacrylate poly(dimethylsiloxane) was added to the mixture before the curing process to modify the toughness of the samples. The mixture was poured into the poly(tetrafluoroethylene) mold; the epoxy resin/curing agent ratio was maintained as 2/1. The clear films formed after microwave irradiation were removed from the mold, cooled, and then stored in a cool and dry medium until characterization. The samples were analyzed by wide angle X-ray diffraction, differential scanning calorimetry, and mechanical tests. Surfaces of the cold fractured samples were also observed under the scanning electron microscope. The results revealed that microwave curing of the samples of 5% organoclay and 5% siloxane showed improvement in mechanical properties. POLYM. ENG. SCI. 46:1104,1110, 2006. © 2006 Society of Plastics Engineers [source] In situ generated diphenylsiloxane-polyimide adduct-based nanocompositesPOLYMER ENGINEERING & SCIENCE, Issue 1 2005Manisha G. Goswami Arylsiloxane was incorporated into polyimide (PI) via electronic interaction with polyamic acid (PAA)/PI, and a wide spectrum of properties were evaluated for different compositions. The samples prepared with relatively low concentrations (0.0001,0.1%) of oligomers showed unusual synergism, which is attributed to the generation of nanostructures dispersed in the continuous PI matrix. The incorporation of siloxane with bulky phenyl groups contributed to enhanced thermal stability as determined by thermogravimetric analysis. Water uptake and methanol absorption by these composites were evaluated and correlated with the underlying micro- and nanostructures. Fourier Transform Infrared (FTIR) spectroscopy was used to elucidate the probable reaction mechanism (including in situ polymerization of arylsilanol), and to study the synthetic aspects associated with the molecular composites and nanocomposites formation. POLYM. ENG. SCI., 45:142,152, 2005. © 2004 Society of Plastics Engineers [source] Morphology and surface properties of some siloxane,organic copolymersPOLYMER INTERNATIONAL, Issue 6 2009Maria Cazacu Abstract BACKGROUND: It is well known that, due to their extremely low polarity, polysiloxanes are incompatible with almost any organic system. This incompatibility leads to phase separation in mixed siloxane,organic systems. RESULTS: Three siloxane,organic copolymers, poly[(5,5,-methylene-bis-salicylaldehyde)-imine-(1,3-bis(propylene)tetramethyldisiloxane)] (Paz1), poly[(2,5-dihydroxy-1,4-benzoquinone)-imine-(1,3-bis(propylene)tetramethyldisiloxane)] (Paz2) and poly[1,3-bis(propylene)tetramethyldisiloxane diamide] (Pam), were prepared by the reaction of 1,3-bis(3-aminopropyl)tetramethyldisiloxane with appropriate organic partners (5,5,-methylene-bis-salicylaldehyde, 2,5-dihydroxy-1,4-benzoquinone and oxalyl chloride, respectively). The morphologies dictated by the incompatibility between siloxane and polar organic moieties were investigated using differential scanning calorimetry and scanning electron microscopy. The surface activity of the copolymers and water vapour sorption capacity were also measured. CONCLUSION: Even though the polar sequences are very short ones, the highly flexible siloxane-containing sequence permits the self-assembly of these into more or less polar domains. Such an organization influences the properties of the resulting materials, an important place being occupied by the surface properties. Copyright © 2009 Society of Chemical Industry [source] Synthesis and characterization of liquid crystalline elastomers bearing fluorinated mesogenic units and crosslinking mesogensPOLYMERS FOR ADVANCED TECHNOLOGIES, Issue 12 2009Fan-Bao Meng Abstract Several new side-chain liquid crystalline (LC) polysiloxanes and elastomers (IP - VIP) bearing fluorinated mesogenic units and crosslinking mesogens were synthesized by a one-step hydrosilylation reaction with poly(methylhydrogeno)siloxane, a fluorine-containing LC monomer 4,-undec-10-enoyloxy-biphenyl-4-yl 4-fluoro-benzoate and a crosslinking LC monomer 4,-(4-allyloxy-benzoxy)-biphenyl-4-yl 4-allyloxy-benzoate. The chemical structures and LC properties of the monomers and polymers were characterized by use of various experimental techniques such as FTIR, 1H-NMR, EA, TGA, DSC, POM and XRD. The effect of crosslinking mesogens on mesomorphic properties of the fluorinated LC polymers was studied as well. The obtained polymers and elastomers were soluble in many solvents such as toluene, tetrahydrofuran, chloroform, and so forth. The temperatures at which 5% weight loss occurred (Td) were greater than 250°C for all the polymers, and the weight of residue near 600°C increased slightly with increase of the crosslinking mesogens in the fluorinated polymer systems. The samples IP, IIP, IIIP and IVP showed both smectic A and nematic phases when they were heated and cooled, but VP and VIP exhibited only a nematic mesophase. The glass transition temperature (Tg) of polymers increased slightly with increase of crosslinking mesogens in the polymer systems, but the mesophase,isotropic phase transition temperature (Ti) and smectic A,nematic mesophase transition temperature (TS-N) decreased slightly. It suggests that the temperature range of the mesophase became narrow with the increase of crosslinking mesogens for all the fluorinated polymers and elastomers. In XRD curves, the intensity of sharp reflections at low angle decreased with increase of crosslinking mesogens in the fluorinated polymers systems, indicating that the smectic order derived from fluorinated mesogenic units should be destroyed by introduction of more crosslinking mesogens. Copyright © 2008 John Wiley & Sons, Ltd. [source] | |||||||||||||||||||||||||||||||