Home About us Contact
|
Home About us Contact | ||
|
|
||
Multifunctional Monomers (multifunctional + monomer)
Selected AbstractsMethacrylate-based monolithic column with mixed-mode hydrophilic interaction/strong cation-exchange stationary phase for capillary liquid chromatography and pressure-assisted CECELECTROPHORESIS, Issue 19 2008Jian Lin Abstract A novel porous polymethacrylate-based monolithic column by in situ copolymerization of 3-sulfopropyl methacrylate (SPMA) and pentaerythritol triacrylate in a binary porogenic solvent consisting of cyclohexanol/ethylene glycol was prepared. The monolith possessed in their structures bonded sulfonate groups and hydroxyl groups and was evaluated as a hydrophilic interaction and strong cation-exchange stationary phases in capillary liquid chromatography (cLC) and pressure-assisted CEC using small polar neutral and charged solutes. While the SPMA was introduced as multifunctional monomer, the pentaerythritol triacrylate was used to replace ethylene glycol dimethacrylate as cross-linker with much more hydrophilicity due to a hydroxyl sub-layer. The different characterization of monolithic stationary phases were specially designed and easily prepared by altering the amount of SPMA in the polymerization solution as well as the composition of the porogenic solvent for cLC and pressure-assisted CEC. The resulting monolith showed the different trends about the effect of the permeabilities on efficiency in the pressure-assisted CEC and cLC modes. A typical hydrophilic interaction chromatography mechanism was observed at higher organic solvent content (ACN%>70%) for polar neutral analytes. For polar charged analytes, both hydrophilic interaction and electrostatic interaction contributed to their retention. Therefore, for charged analytes, selectivity can be readily manipulated by changing the composition of the mobile phase (e.g., pH, ionic strength and organic modifier). With the optimized monolithic column, high plate counts reaching greater than 170,000,plates/m for pressure-assisted CEC and 105,000 plates/m for cLC were easily obtained, respectively. [source] Comparison of monofunctional and multifunctional monomers in phosphate binding molecularly imprinted polymersJOURNAL OF MOLECULAR RECOGNITION, Issue 6 2008Xiangyang Wu Abstract In this study, molecularly imprinted polymers (MIPs) prepared using a multifunctional and a monofunctional monomer were compared with respect to their affinities, selectivities, and imprinting efficiencies for organophosphates. This is of interest because multifunctional monomers have higher affinities than traditional monofunctional monomers for their target analytes and thus should yield MIPs with higher affinities and selectivities. However, polymers containing multifunctional monomer may also have a higher number of unselective, non-templated binding sites. This increase in background binding sites could lead to a decrease in the magnitude of the imprinting effect and in the selectivity of the MIP. Therefore, phosphate selective imprinted and non-imprinted polymers (NIPs) were prepared using a novel multifunctional triurea monomer. The binding properties of these polymers were compared with polymers prepared using a monofunctional monourea monomer. The binding affinities and selectivities of the monomers, imprinted polymers, and NIPs were characterized by NMR titration, binding uptake studies, and binding isotherms. MIPs prepared with the triurea monomer showed higher binding affinity and selectivity for the diphenylphosphate anion in organic solvents than the MIPs prepared with the monofunctional monomer. Surprisingly, the binding properties of the NIPs revealed that the polymers prepared using the multifunctional and monofunctional monomers were very similar in affinity and selectivity. Thus, the multifunctional monomers increase not only the affinity of the MIP but also enhance the imprinting effect. Copyright © 2008 John Wiley & Sons, Ltd. [source] Cover Picture: TiO2 Nanoparticle,Photopolymer Composites for Volume Holographic Recording (Adv. Funct.ADVANCED FUNCTIONAL MATERIALS, Issue 10 2005Mater. Abstract TiO2 nanoparticle,photopolymer composites have been employed for volume holographic recording, as reported by Sánchez and co-workers on p.,1623. Photoinduced segregation of the high refractive index, grafted nanoparticles between polymer-rich areas leads to improved refractive-index modulation amplitudes with respect to the base material without nanoparticles. The cover schematically shows a holographic grating registered in this nanocomposite material. These nanocomposite materials should enable the production of holographic optical elements to efficiently control light with angle and wavelength selectivity. This could be used, for example, in liquid-crystal display technology. A new and efficient photopolymer for the recording of volume holograms is presented. The material comprises a mixture of UV-sensitive acrylates and grafted titanium dioxide nanoparticles with an average size of 4,nm. We report the formation of holographic gratings with refractive-index modulation amplitudes of up to 15.5,×,10,3,an improvement of more than a factor of four over the base material without nanoparticles,while maintaining a low level of scattering and a high transparency in the visible-wavelength range. The influence of the composition of the acrylate system on the final properties of the holographic material is also investigated and discussed. The presence of multifunctional monomers favors the compositional segregation of the different components, while the addition of monofunctional acrylate, highly compatible with the grafting of the nanoparticles, favors the dilution of these nanoparticles. [source] Synthesis, characterization, and cure reaction of methacrylate-based multifunctional monomers for dental compositesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2007Mousa Ghaemy Abstract The synthesis of 2,2-bis[(4-(2-hydroxy-3-methacryloxyethoxy)phenyl]propane (BHEP) and (1-methacryloxy-3-ethoxymethacryloxy-2-hydroxy)propane (MEHP) for use as the monomer phase in dental composites are reported. The monomers were prepared by the reaction of 2-hydroxyethyl methacrylate (HEMA) with diglycidyl-ether of bisphenol A (DGEBA) and with glycidyl methacrylate (GMA), respectively. The progress of the reaction was followed by measuring the disappearance of the epoxide group peak using FTIR and the structure of the monomers was characterized by 1H-NMR. BHEP and MEHP have lower viscosity because of the presence of long aliphatic spacer on both sides of the aromatic ring in BHEP and the absence of aromatic rings and the presence of only one hydroxyl group in each molecule of MEHP. Thermal curing of the monomers was conducted in a DSC using benzoyl peroxide as an initiator. Photopolymerization of the monomers was also conducted with the visible light using camphorquinone and N,N -dimethylaminoethyl methacrylate as the photoinitiating system. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 [source] Comparison of monofunctional and multifunctional monomers in phosphate binding molecularly imprinted polymersJOURNAL OF MOLECULAR RECOGNITION, Issue 6 2008Xiangyang Wu Abstract In this study, molecularly imprinted polymers (MIPs) prepared using a multifunctional and a monofunctional monomer were compared with respect to their affinities, selectivities, and imprinting efficiencies for organophosphates. This is of interest because multifunctional monomers have higher affinities than traditional monofunctional monomers for their target analytes and thus should yield MIPs with higher affinities and selectivities. However, polymers containing multifunctional monomer may also have a higher number of unselective, non-templated binding sites. This increase in background binding sites could lead to a decrease in the magnitude of the imprinting effect and in the selectivity of the MIP. Therefore, phosphate selective imprinted and non-imprinted polymers (NIPs) were prepared using a novel multifunctional triurea monomer. The binding properties of these polymers were compared with polymers prepared using a monofunctional monourea monomer. The binding affinities and selectivities of the monomers, imprinted polymers, and NIPs were characterized by NMR titration, binding uptake studies, and binding isotherms. MIPs prepared with the triurea monomer showed higher binding affinity and selectivity for the diphenylphosphate anion in organic solvents than the MIPs prepared with the monofunctional monomer. Surprisingly, the binding properties of the NIPs revealed that the polymers prepared using the multifunctional and monofunctional monomers were very similar in affinity and selectivity. Thus, the multifunctional monomers increase not only the affinity of the MIP but also enhance the imprinting effect. Copyright © 2008 John Wiley & Sons, Ltd. [source] Study of Laser-Induced Photopolymerizations by Optical PyrometryMACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 15 2004Patrick Lin Abstract Summary: Studies of the 355 nm laser induced free radical and cationic photopolymerization reactions of mono- and multifunctional monomers were conducted. These investigations were carried out with the aid of a specially constructed optical pyrometry instrument that provides rapid, reproducible temperature versus time profiles for these fast photopolymerization reactions. Using this technique, the effects of various reaction parameters and monomer structures on the rate and extent of the photopolymerization reactions were examined. Optical pyrometry instrument for the monitoring of laser-induced photopolymerizations. [source] Kinetic Study and New Applications of UV Radiation CuringMACROMOLECULAR RAPID COMMUNICATIONS, Issue 18 2002Christian Decker Abstract Highly crosslinked polymers can be readily synthesized by photoinitiated polymerization of multifunctional monomers or functionalized polymers. The reaction can be followed in situ by real-time infrared (RT-IR) spectroscopy, a technique that records conversion versus time curves in photosensitive resins undergoing ultrafast polymerization upon UV exposure. For acrylate-based resins, UV-curing proceeds with long kinetic chains (7700 mol/radical) in spite of the high initiation rate. RT-IR spectroscopy proved very valuable in assessing the influence of various parameters, such as initiation efficiency, chemical structure of the telechelic oligomer, light intensity, inhibitory effect of oxygen, on polymerization kinetics. Interpenetrating polymer networks can be rapidly synthesized by means of UV irradiation of a mixture of difunctional acrylate and epoxy monomers in the presence of both radical and cationic-type photoinitiators. The same UV technology can be applied to crosslink solid polymers at ambient temperature, which bear different types of reactive groups (acrylate and vinyl double bonds, epoxy ring). UV radiation curing has been successfully used to produce within seconds weathering resistant protective coatings, high-resolution relief images, glass laminates and nanocomposites materials. Photoinitiated crosslinking polymerization. [source] Light-induced crosslinking polymerization,POLYMER INTERNATIONAL, Issue 11 2002Christian Decker Abstract Light-induced polymerization of multifunctional monomers is a powerful method to transform a liquid resin into a solid polymer almost instantly, selectively in the illuminated areas. The reaction can conveniently be followed by real-time infrared spectroscopy, a technique which records directly conversion versus time curves in photosensitive resins undergoing ultrafast curing upon UV or laser exposure. The photoinitiator was shown to play a key role in laser-induced polymerization because of the monochromatic character of the emitted radiation. By using highly sensitive acrylate photoresists, relief images of micronic size were obtained by fast scanning with a focused laser beam. The laser direct imaging technology makes image transfer obsolete and eliminates the manufacture of photolithographic masks. Polymer networks of different architectures have been obtained by UV irradiation of various monomer blends: acrylate,epoxide, acrylate,vinyl ether, acrylate,polyene, vinyl ether,maleate and thiol,polyene. With monomers polymerizing by different mechanisms, ie radical and cationic types, interpenetrating polymer networks have been generated upon UV exposure in the presence of adequate photoinitiators. The crosslinking reaction was also performed in the solid state on polybutadiene which was plasticized with a multifunctional acrylate or thiol monomer. Thermoplastic elastomers were transformed within a fraction of a second into an insoluble material showing a greatly improved resistance to heat and chemicals, because of the tight polymer network formed. © 2002 Society of Chemical Industry [source] | ||||||||||