کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5180455 | 1502544 | 2015 | 11 صفحه PDF | دانلود رایگان |
- Analysis of algorithms to produce cross-linked phenolic structures.
- Iterative cross-linking approach produced low variability high cross-linked configurations.
- Algorithm parameters influence the final densities and energetics of cross-linked phenolic.
- Mechanical and thermal properties depend strongly on density and degree of cross-linking.
- Good agreement with experiments was found for thermal conductivity and Young's modulus.
Algorithms to generate atomistic models of cross-linked phenolic resins suitable for molecular dynamics simulations were investigated. The influence of five parameters (initial volume of uncross-linked material, cross-linking approach, relaxation time, equilibration temperature) on generating cross-linked structures was studied quantitatively using a full factorial sensitivity analysis. The parameters were found to be dependent on the degree of cross linking (D). For low cross-linking, only the equilibration temperature has a significant impact on the final energetics and densities. However, for higher cross-linking (DÂ >Â 70%), the equilibration temperature, initial volume and cross-linking approach were shown to influence the phenolic structures. Iterative, rather than single step, methods were shown to produce better structures. The initial volume of the uncross-linked material was identified as having the most influence on the final volume of fully cross-linked systems. By optimizing all five parameters, highly cross-linked samples with low energetics and consistent densities could be generated. To validate the models, thermo-mechanical properties of cross-linked phenolic samples were characterized as a function of density and degree of cross-linking. Good agreement with experimental values was obtained for properties such as the glass transition temperature, coefficient of thermal expansion (CTE), elastic moduli, and thermal conductivity.
Journal: Polymer - Volume 62, 7 April 2015, Pages 39-49