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Bifunctional Initiator (bifunctional + initiator)
Selected AbstractsMicrophase-Separated Poly(vinylpyridine) Block Copolymer Prepared with a Novel Bifunctional InitiatorMACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 7 2009Masami Shoji Abstract A vinylpyridine block copolymer was prepared by stepwise controlled/living radical polymerization with a novel bifunctional initiator, 4-(2-bromopropanoyloxy)- N -(p -methylbenzyloxy)-2,2,6,6-tetramethylpiperidine. The initiator was synthesized in a facile manner using commercially available p -xylene and 4-hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (4-hydroxy TEMPO). Through stepwise atom transfer radical polymerization (ATRP) of methyl methacrylate (MMA) and nitroxide-mediated radical polymerization (NMRP) of 4-vinylpyridine (4VP), the PMMA- b- P4VP copolymer was prepared with a wide range of the copolymer compositions. Microphase-separation was demonstrated in cross sectional TEM images of self-standing block copolymer membranes. [source] Atom Transfer Radical Polymerization of Styrene Using a Bifunctional InitiatorCHINESE JOURNAL OF CHEMISTRY, Issue 9 2001Jin-Ying Yuan Abstract A bifunctional alkyl halide, namely l, 2-bis(2,-bromobutyryl) ethane (BBrBE), was synthesized and used to initiate the bulk atom transfer radical polymerization (ATRP) of styrene (St) at 110°C in the presence of CuBr/2,2,-bipyridyl. The narrow polydispersity of polystyrene (PSt) with precisely two arms could be synthesized. The initiate ability of the two active bromide functional groups at both sides of BBrBE for St and the propagation ability of the two arms were confirmed to be similar by the characterization of the individual arms obtained upon hydrolysis of the ester link between the core and the branches. [source] Mathematical Modeling of Atom-Transfer Radical Polymerization Using Bifunctional InitiatorsMACROMOLECULAR THEORY AND SIMULATIONS, Issue 3 2006Mamdouh Al-Harthi Abstract Summary: Bifunctional initiators can produce polymers with higher molecular weight at higher initiator concentrations than monofunctional initiators. In this study, we developed a mathematical model for ATRP with bifunctional initiators. The most important reactions in ATRP were included in the model. The method of moments was used to predict monomer conversion, average molecular weights and polydispersity index as a function of polymerization time in batch reactors. The model was used to understand the mechanism of ATRP and to quantify how polymerization conditions affect monomer conversion and polymer properties by examining the effect of several rate constants (activation, deactivation, propagation and chain termination) and of catalyst and initiator concentration on polymerization kinetics and polymer properties. When compared to monofunctional initiators, bifunctional initiators not only produce polymers with higher molecular weight averages at higher polymerization rates, but also control their molecular weight distributions more effectively. Effect of initial catalyst concentration on polydispersity index as a function of time. [source] Analyzing the real advantages of bifunctional initiator over monofunctional initiator in free radical polymerizationJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2010Paula F. de M. P. B. Machado Abstract Monofunctional initiators are extensively used in free radical polymerization. To enhance productivity, a higher temperature is usually used; however, this leads to lower molecular weights. Bifunctional initiators can increase the polymerization rate without decreasing the average molecular weight and this can be desirable. A bifunctional initiator is an important issue to be investigated, and it is of great interest to industries. The objective of this work is to study polymerization reactions with mono- and bi-functional initiators through comprehensive mathematical models. Polystyrene is considered as case study. This work collects and presents some experimental data available in literature for polymerization using two different types of bifunctional initiators. Model prediction showed good agreement with experimental data. It was observed that the initial initiator concentration has a huge impact on the efficiency of initiators with functionality bigger than one and high concentrations of bifunctional initiator make the system behave as if it were a system operating with monofunctional initiator. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Mathematical Modeling of Atom-Transfer Radical Polymerization Using Bifunctional InitiatorsMACROMOLECULAR THEORY AND SIMULATIONS, Issue 3 2006Mamdouh Al-Harthi Abstract Summary: Bifunctional initiators can produce polymers with higher molecular weight at higher initiator concentrations than monofunctional initiators. In this study, we developed a mathematical model for ATRP with bifunctional initiators. The most important reactions in ATRP were included in the model. The method of moments was used to predict monomer conversion, average molecular weights and polydispersity index as a function of polymerization time in batch reactors. The model was used to understand the mechanism of ATRP and to quantify how polymerization conditions affect monomer conversion and polymer properties by examining the effect of several rate constants (activation, deactivation, propagation and chain termination) and of catalyst and initiator concentration on polymerization kinetics and polymer properties. When compared to monofunctional initiators, bifunctional initiators not only produce polymers with higher molecular weight averages at higher polymerization rates, but also control their molecular weight distributions more effectively. Effect of initial catalyst concentration on polydispersity index as a function of time. [source] Analyzing the real advantages of bifunctional initiator over monofunctional initiator in free radical polymerizationJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2010Paula F. de M. P. B. Machado Abstract Monofunctional initiators are extensively used in free radical polymerization. To enhance productivity, a higher temperature is usually used; however, this leads to lower molecular weights. Bifunctional initiators can increase the polymerization rate without decreasing the average molecular weight and this can be desirable. A bifunctional initiator is an important issue to be investigated, and it is of great interest to industries. The objective of this work is to study polymerization reactions with mono- and bi-functional initiators through comprehensive mathematical models. Polystyrene is considered as case study. This work collects and presents some experimental data available in literature for polymerization using two different types of bifunctional initiators. Model prediction showed good agreement with experimental data. It was observed that the initial initiator concentration has a huge impact on the efficiency of initiators with functionality bigger than one and high concentrations of bifunctional initiator make the system behave as if it were a system operating with monofunctional initiator. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Novel synthesis of rod-coil block copolymers by combination of coordination polymerization and ATRPJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 17 2007Koji Ishizu Abstract Combination of coordination polymerization and atom transfer radical polymerization (ATRP) was applied to a novel synthesis of rod-coil block copolymers. The procedure included the following steps: (1) monoesterification reaction of ethylene glycol with 2-bromoisobutyryl bromide yielded a ,-bromo, ,-hydroxy bifunctional initiator, (2) CpTiCl3 (bifunctional initiator) catalyst was prepared from a mixture of trichlorocyclopentadienyl titanium (CpTiCl3) and bifunctional initiator. Coordination polymerization of n- butyl isocyanate initiated by such catalyst provided a well-defined macroinitiator, poly(n- butyl isocyanate)-Br (PBIC-Br), and (3) ATRP method of vinyl monomers using PBIC-Br provided rod (PBIC)-coil block copolymers. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 4037,4042, 2007 [source] Microphase-Separated Poly(vinylpyridine) Block Copolymer Prepared with a Novel Bifunctional InitiatorMACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 7 2009Masami Shoji Abstract A vinylpyridine block copolymer was prepared by stepwise controlled/living radical polymerization with a novel bifunctional initiator, 4-(2-bromopropanoyloxy)- N -(p -methylbenzyloxy)-2,2,6,6-tetramethylpiperidine. The initiator was synthesized in a facile manner using commercially available p -xylene and 4-hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (4-hydroxy TEMPO). Through stepwise atom transfer radical polymerization (ATRP) of methyl methacrylate (MMA) and nitroxide-mediated radical polymerization (NMRP) of 4-vinylpyridine (4VP), the PMMA- b- P4VP copolymer was prepared with a wide range of the copolymer compositions. Microphase-separation was demonstrated in cross sectional TEM images of self-standing block copolymer membranes. [source] Analyzing the real advantages of bifunctional initiator over monofunctional initiator in free radical polymerizationJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2010Paula F. de M. P. B. Machado Abstract Monofunctional initiators are extensively used in free radical polymerization. To enhance productivity, a higher temperature is usually used; however, this leads to lower molecular weights. Bifunctional initiators can increase the polymerization rate without decreasing the average molecular weight and this can be desirable. A bifunctional initiator is an important issue to be investigated, and it is of great interest to industries. The objective of this work is to study polymerization reactions with mono- and bi-functional initiators through comprehensive mathematical models. Polystyrene is considered as case study. This work collects and presents some experimental data available in literature for polymerization using two different types of bifunctional initiators. Model prediction showed good agreement with experimental data. It was observed that the initial initiator concentration has a huge impact on the efficiency of initiators with functionality bigger than one and high concentrations of bifunctional initiator make the system behave as if it were a system operating with monofunctional initiator. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Mathematical Modeling of Atom-Transfer Radical Polymerization Using Bifunctional InitiatorsMACROMOLECULAR THEORY AND SIMULATIONS, Issue 3 2006Mamdouh Al-Harthi Abstract Summary: Bifunctional initiators can produce polymers with higher molecular weight at higher initiator concentrations than monofunctional initiators. In this study, we developed a mathematical model for ATRP with bifunctional initiators. The most important reactions in ATRP were included in the model. The method of moments was used to predict monomer conversion, average molecular weights and polydispersity index as a function of polymerization time in batch reactors. The model was used to understand the mechanism of ATRP and to quantify how polymerization conditions affect monomer conversion and polymer properties by examining the effect of several rate constants (activation, deactivation, propagation and chain termination) and of catalyst and initiator concentration on polymerization kinetics and polymer properties. When compared to monofunctional initiators, bifunctional initiators not only produce polymers with higher molecular weight averages at higher polymerization rates, but also control their molecular weight distributions more effectively. Effect of initial catalyst concentration on polydispersity index as a function of time. [source] | ||||||||||