2008
DOI: 10.1016/j.polymer.2008.01.037
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Structure–property relationships of controlled epoxy networks with quantified levels of excess epoxy etherification

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Cited by 34 publications
(36 citation statements)
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“…Some authors confirm that the etherification reaction can occur under specific conditions (i) at temperatures higher than 150 °C25, 26 and (ii) with an epoxide conversion above 90% 24, 27, 28. Indeed, the etherification reaction takes place at intermediate and high reaction extents, when the amount of hydroxyl groups in the system is high enough and the primary amine content has been reduced 17, 29. It is also the case when the epoxide groups are in stoichiometric excess 29.…”
Section: Resultsmentioning
confidence: 94%
See 1 more Smart Citation
“…Some authors confirm that the etherification reaction can occur under specific conditions (i) at temperatures higher than 150 °C25, 26 and (ii) with an epoxide conversion above 90% 24, 27, 28. Indeed, the etherification reaction takes place at intermediate and high reaction extents, when the amount of hydroxyl groups in the system is high enough and the primary amine content has been reduced 17, 29. It is also the case when the epoxide groups are in stoichiometric excess 29.…”
Section: Resultsmentioning
confidence: 94%
“…Indeed, the etherification reaction takes place at intermediate and high reaction extents, when the amount of hydroxyl groups in the system is high enough and the primary amine content has been reduced 17, 29. It is also the case when the epoxide groups are in stoichiometric excess 29. Moreover, the homopolymerization of glycidyl groups, the fourth potential reaction, which requires the presence of Lewis bases (i.e., tertiary amines) or Lewis acid catalysts (i.e., BF 3 complexed with an amine), was considered negligible.…”
Section: Resultsmentioning
confidence: 99%
“…It was seen that as M C increased in the system the higher the K IC value became. Sherman et al [27] attribute this to an increase in the free volume of the materials, which allows more space resulting in an increase of chain motions capable to accommodate the applied load. Nevertheless, linear correlation was not found for the system under study, the results showed that the K IC values did not increase as M C increased.…”
Section: Determination Of Average Molecularmentioning
confidence: 99%
“…The epoxide ring is highly reactive to amines and crosslinks with other epoxy monomers by the ring opening polymerization process, which results in a crosslinked polymer [12–15]. As this crosslinked polymer is difficult to recycle once its useful life is over, it is usually disposed of in landfill sites [16, 17], thereby affecting the environment. Consequently, in this study, we look at alternate ways to recycle the epoxy polymer.…”
Section: Introductionmentioning
confidence: 99%