2015
DOI: 10.3390/polym7040680
|View full text |Cite
|
Sign up to set email alerts
|

Enhancement in the Glass Transition Temperature in Latent Thiol-Epoxy Click Cured Thermosets

Abstract: Tri and tetrafunctional thiol were used as curing agent for diglycidyl ether of bisphenol A (DGEBA) catalyzed by a commercially available amine precursor, LC-80. Triglycidyl isocianurate (TGIC) was added in different proportions to the mixture to increase rigidity and glass transition temperature (Tg). The cooperative effect of increasing functionality of thiol and the presence of TGIC in the formulation leads to an increased Tg without affecting thermal stability. The kinetics of the curing of mixtures was st… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

6
37
0

Year Published

2015
2015
2024
2024

Publication Types

Select...
9

Relationship

3
6

Authors

Journals

citations
Cited by 41 publications
(43 citation statements)
references
References 16 publications
6
37
0
Order By: Relevance
“…A negative side effect would be that the exothermicity of the second process would increase because of the higher excess of epoxy groups, but the reaction rate would still be low and therefore the crosslinking process could be easily controlled anyway. In addition, one can use other epoxy monomers/resins and change the amount of initiator or type of catalyst to control the reactivity of the curing process. Other dual‐curing thermosetting systems such as off‐stoichiometric thiol–acrylate or epoxy–amine could be used as well, providing suitable catalysts or initiators were used to activate the curing reactions in a controlled way in order to achieve a SHR and therefore enable easy thermal management during processing.…”
Section: Resultsmentioning
confidence: 99%
“…A negative side effect would be that the exothermicity of the second process would increase because of the higher excess of epoxy groups, but the reaction rate would still be low and therefore the crosslinking process could be easily controlled anyway. In addition, one can use other epoxy monomers/resins and change the amount of initiator or type of catalyst to control the reactivity of the curing process. Other dual‐curing thermosetting systems such as off‐stoichiometric thiol–acrylate or epoxy–amine could be used as well, providing suitable catalysts or initiators were used to activate the curing reactions in a controlled way in order to achieve a SHR and therefore enable easy thermal management during processing.…”
Section: Resultsmentioning
confidence: 99%
“…Tertiary amines are commonly used as base catalysts in thiol-epoxy formulations, but they are usually too reactive, making it hard to control the reaction and shortening their pot-life. It was recently shown [25,26] that it is possible to increase the pot life of thiol-epoxy formulations by means of polymer-encapsulated amines or thermally stable aromatic-aliphatic ureas, being the former the most effective way. Thus, it is possible to prepare formulations, store them safely before application, and process them at temperatures high enough to quickly release the amine catalyst and produce a completely cured material in a short period of time.…”
Section: Introductionmentioning
confidence: 99%
“…Other typical hardeners of epoxy resins are polythiols [156][157][158][159] and polyisocyanates [160][161][162][163]. Like carboxylic acids, their nucleophilicity is usually much lower than amines or dihydrazides and base-catalyzed conditions must be used to observe adequate curing rates.…”
Section: Thiols and Isocyanatesmentioning
confidence: 99%