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Cured Material (cured + material)
Selected AbstractsNew thermosets obtained by the cationic copolymerization of diglycidyl ether of bisphenol A with ,-caprolactone with an improvement in the shrinkage.JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 10 2007Abstract Diglycidyl ether of bisphenol A was cured with different proportions of ,-caprolactone with ytterbium triflate as an initiator. The curing was studied by means of differential scanning calorimetry and Fourier transform infrared in the attenuated total reflection mode. The latter was used to monitor the competitive reactive processes and to quantify the conversions of the epoxide, lactone, and intermediate spiroorthoester groups. A partial depolymerization process from the cured material to free ,-caprolactone was also identified. The formation of a stable carbocation and the coordinative capability of ytterbium triflate were the reasons for this unexpected process. The thermal and dynamic mechanical properties of the cured materials were determined with differential scanning calorimetry, thermogravimetric analysis, and dynamic mechanical thermal analysis. An increase in the proportion of ,-caprolactone resulted in an increased curing rate, a decrease in the shrinkage after gelation, and a significant decrease in the glass transition temperature. The introduction of ester linkages into the three-dimensional structure led to more thermally degradable thermosets. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 1968,1979, 2007 [source] A Quantum-Mechanical QSAR Model to Predict the Refractive Index of Polymer MatricesMOLECULAR INFORMATICS, Issue 10 2006Andrew Abstract Refractive index (RI) is an important optical property for polymer matrices, especially when the color or tint of the cured material is of interest. This is certainly the case for dental restorative applications. In this work, results are presented for a quantitative,structure activity relationship derived from relevant semiempirical quantum mechanical information. This model predicts the RI for a wide variety of polymer matrices using representative structures of polymers, including resin components of several currently used dental restorative materials. The AM1 semiempirical method was used for calculations due to its speed and general reliability. Several structural subunits of the polymer chains were used for the QSAR analysis, but dimer moieties produced the best results for some 60 polymers. The final QSAR model was composed of a multilinear equation that featured the highest occupied molecular orbital , the lowest unoccupied molecular orbital gap and a polarizability index as the two descriptors best able to account for the variation in the data. The final model had R2=0.963, R2cv=0.959, F=740, and s2=0.0002. Other quality indicators for the correlation and the individual descriptors were within acceptable limits. The presence of electronically related descriptors is encouraging, as these are conceptually tied to the phenomenon of RI. The difference between a theoretically predicted value for poly(propylene oxide) and its monomer was 0.04, as compared to 0.09 from experimental data. [source] Spectroscopic ellipsometry and ellipsometric porosimetry studies of CVD low-k dielectric filmsPHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 5 2008P. Marsik Abstract Aurora® ELK, a porous low-k SiCOH film deposited by CVD, was used to study the effect of UV curing. Samples were cured for various curing times and the purpose of this work is to observe the effects of UV curing on optical, mechanical and structural properties of the low-k film. We have used 1) ellipsometric porosimetry to determine the porosity and the pore-size distribution and 2) nitrogen purged UV ellipsometry in a range from 2 to 9 eV to observe the changes of the dielectric function of the cured material. Additional FTIR and laser-induced surface acoustic wave measurements were performed. The porogen removal and the increase of porosity were observed, and a k-value of 2.3 was reached for the optimum curing time. However for longer curing times, densification and reduction of the porosity occurs. The growth of the hydrogen incorporation has been observed. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Kinetic study of the curing of mixtures of DGEBA and five-membered cyclic carbonates with lanthanum triflate as cationic initiatorJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2007Roser Cervellera Abstract Mixtures of diglycidylether of bisphenol A (DGEBA) with 1,3-benzodioxolane-2-one (CC) or 4-phenoxymethyl-1,3-dioxolane-2-one (PGEC) were cured in the presence of lanthanum triflate. FTIR/ATR was used to study the evolution of carbonate and epoxide groups to follow the reactive processes that take place during curing. DSC was applied to study the thermal characteristics of the curing process and to determine the glass-transition temperatures of the cured materials. The kinetics of the curing was studied isothermally by means of FTIR and the kinetic model was selected through the isokinetic relationships. DSC experiments were used to study the kinetics in nonisothermal conditions by means of isoconversional procedures and the Coats,Redfern and Criado methodologies. By TMA we could monitor the evolution of the shrinkage during isothermal curing. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2875,2884, 2007 [source] New thermosets obtained by the cationic copolymerization of diglycidyl ether of bisphenol A with ,-caprolactone with an improvement in the shrinkage.JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 10 2007Abstract Diglycidyl ether of bisphenol A was cured with different proportions of ,-caprolactone with ytterbium triflate as an initiator. The curing was studied by means of differential scanning calorimetry and Fourier transform infrared in the attenuated total reflection mode. The latter was used to monitor the competitive reactive processes and to quantify the conversions of the epoxide, lactone, and intermediate spiroorthoester groups. A partial depolymerization process from the cured material to free ,-caprolactone was also identified. The formation of a stable carbocation and the coordinative capability of ytterbium triflate were the reasons for this unexpected process. The thermal and dynamic mechanical properties of the cured materials were determined with differential scanning calorimetry, thermogravimetric analysis, and dynamic mechanical thermal analysis. An increase in the proportion of ,-caprolactone resulted in an increased curing rate, a decrease in the shrinkage after gelation, and a significant decrease in the glass transition temperature. The introduction of ester linkages into the three-dimensional structure led to more thermally degradable thermosets. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 1968,1979, 2007 [source] |