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Weight Averages (weight + average)
Kinds of Weight Averages Terms modified by Weight Averages Selected AbstractsSyntheses of aliphatic polyesters catalyzed by lanthanide triflatesJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 1 2009Mazen Garaleh Abstract Polycondensations of 1,6-hexane diol and sebacic acid were conducted in bulk with addition of a lanthanide triflate as acidic catalyst. With exception of promethium triflate all lanthanide triflates were studied. A particularly low molecular weight was obtained with neodym triflate and the best results with samarium triflate. With Sm(OTf)3 weight average (Mw) values up to 65 kDa (uncorrected SEC data) were achieved after optimization of the reaction conditions. Comparison of these results with those obtained from bismuth, magnesium, and zinc triflates, on the one hand, and comparison with the acidities of all catalysts, on the other, indicates that the esterification mechanism involves complexation of monomer by metal ions. Preparation of multiblock copoly(ether ester)s failed due to insufficient incorporation of poly(tetrahydrofuran) diols. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 170,177, 2009 [source] Mean-Square Radius of Gyration and Degree of Branching of Highly Branched Copolymers Resulting from the Copolymerization of AB2 With AB MonomersMACROMOLECULAR THEORY AND SIMULATIONS, Issue 8 2004Zhiping Zhou Abstract Summary: The evolution of the various structural units incorporated into hyperbranched polymers formed from the copolymerization of AB2 and AB monomers has been derived by the kinetic scheme. The degree of branching was calculated with a new definition given in this work. The degree of branching monotonously increased with increasing A group conversion (x) and the maximum value could reach 2r/(1,+,r)2, where r is the initial fraction of AB2 monomers in the total. Like the average degree of polymerization, the mean-square radius of gyration of the hyperbranched polymers increased moderately with A group conversion in the range x,<,0.9 and displayed an abrupt rise when the copolymerization neared completion. The characteristic ratio of the mean-square radius of gyration remained constant for the linear polymers. However, the hyperbranched polymers did not possess this character. In comparison with the linear polymerization, the weight average and z -average degree of polymerization increased due to the addition of the branched monomer units AB2 and the mean-square radius of gyration decreased quickly for the products of copolymerization. [source] 4-Acetoxystyrene nitroxide-mediated controlled radical polymerization: Comparison with styreneJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2010Andrew S. Cho Abstract The nitroxide-mediated controlled radical polymerization (NM-CRP) of 4-acetoxystyrene with an alkoxyamine was analyzed by a combined experimental and modeling approach. At low nitroxide concentrations, thermal initiation was significant, and control of the polydispersity was poor, as was observed previously for styrene. A continuum model based on the method of moments was used to regress the parameters for the reversible nitroxide uncoupling/coupling reactions (activation energy of uncoupling), thermal initiation (activation energy of initiation), and termination (frequency factor of recombination). The model was able to capture the molecular weight averages and the polydispersity index as a function of time and the nitroxide concentration qualitatively and quantitatively. Using this mechanistic framework, we developed kinetic Monte Carlo models that allowed the molecular weight distributions to be predicted explicitly in good agreement with experimental data. A comparison of the NM-CRP of 4-acetoxystyrene and styrene is provided to illustrate the effect of the acetoxy substituent. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Terpolymerization monitoring with ATR-FTIR spectroscopyJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 11 2001Hong Hua Abstract Butyl acrylate, methyl methacrylate, and vinyl acetate solution and emulsion terpolymerizations were conducted. Attenuated total relflection-Fourier transform infrared spectroscopy equipped with conduit and diamond-composite sensor technology was used to monitor solution terpolymerizations off-line and emulsion terpolymerizations in-line. Monomer conversion and terpolymer composition changes as a function of time were calculated by monitoring the peak height of characteristic absorbances of each monomer. Results obtained from the ReactIRÔ 1000 reaction-analysis system agreed well with those determined by traditional gravimetry and 1H NMR spectroscopy. For the solution terpolymerizations, improved models developed previously to incorporate solvent effects on solution polymerizations of butyl acrylate and vinyl acetate monomers were applied to predict monomer conversion, copolymer composition, and molecular weight averages. Comparisons between experimental data and model predictions are presented. © 2001 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 39: 1860,1876, 2001 [source] Determination of molecular weight distribution parameters of polymers and additives by field desorption mass spectrometryLUBRICATION SCIENCE, Issue 2 2002K. Vivekanandan Abstract The applicability of the field desorption mass spectrometry (FD-MS) technique to the determination of the molecular weight distribution parameters of various commercially available petroleum sulphonates is demonstrated. The technique has been substantiated using standards such as polyethylene glycols, polystyrenes, and sodium petroleum sulphonates. This study of molecular weight averages compares the results from gel permeation chromatography and FD-MS. [source] An Experimental Study on the Free-Radical Copolymerization Kinetics with Crosslinking of Styrene and Divinylbenzene in Supercritical Carbon DioxideMACROMOLECULAR REACTION ENGINEERING, Issue 1 2009Pedro R. García-Morán Abstract A study on the effect of process conditions and composition of the reacting mixture on the kinetics and particle properties in the copolymerization of styrene and divinylbenzene in supercritical carbon dioxide is presented. Polystyrene -block- polydimethylsiloxane and Krytox 257 FSL (Dupont) were used as stabilizers, and their performance compared. A 38 mL, high-pressure view cell, equipped with one frontal and two lateral sapphire windows, was used as the reacting vessel. The polymer product was characterized for total monomer conversion, gel content, molecular weight averages of the sol fraction and particle size distribution. Acceptable polymerization rates and partially-agglomerated spherical particles were produced under the conditions tested. [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] | ||||||||||