1956
DOI: 10.1002/jctb.5010060807
|View full text |Cite
|
Sign up to set email alerts
|

Chemical and spectroscopic studies of epoxy resin reactions in the surface coating field

Abstract: Esterification of epoxy resins with fatty acids at 260° occurs in two stages (1) addition of one fatty acid molecule to an epoxy group to form a hydroxy‐ester, (2) esterification of the original and of the so‐formed hydroxy groups. The curing process of epoxy resins with amines has been studied by infra‐red spectroscopy, and by measurement of the material produced which is non‐extractable by solvents. The combined data provide some indication of the curing mechanism.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
8
0

Year Published

1967
1967
2017
2017

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations
Cited by 50 publications
(8 citation statements)
references
References 5 publications
0
8
0
Order By: Relevance
“…49 Applying BlocBuilder to control GMA-containing feeds is problematic as the epoxy functionality in the monomer could react with the carboxylic acid attached to BlocBuilder, leading to branched, insoluble products. Indeed, the epoxy/carboxylic acid reaction has long been widely used in curing systems 50 and in reactive compatibilization. 51,52 Our earlier work did not indicate any sort of premature cross-linking, likely due to the dilution of the acid end group from the macroinitiator.…”
Section: Introductionmentioning
confidence: 99%
“…49 Applying BlocBuilder to control GMA-containing feeds is problematic as the epoxy functionality in the monomer could react with the carboxylic acid attached to BlocBuilder, leading to branched, insoluble products. Indeed, the epoxy/carboxylic acid reaction has long been widely used in curing systems 50 and in reactive compatibilization. 51,52 Our earlier work did not indicate any sort of premature cross-linking, likely due to the dilution of the acid end group from the macroinitiator.…”
Section: Introductionmentioning
confidence: 99%
“…It has been shown [14][15][16][17] that in the absence of catalysts, epoxy/anhydride polymerization reactions occur mainly through consecutive addition/esterification steps, leading to a crosslinked polyester network. The mechanism involves the attack of hydroxyl groups of the epoxy resin on the anhydride molecules to form a monoester having a free carboxyl group.…”
Section: Resultsmentioning
confidence: 99%
“…An uncatalyzed reaction pathway may be possible due to the presence of hydroxyl groups on the epoxy resins or from impurities in the raw materials. However, in most cases, the use of catalyst is necessary to ensure an efficient polymerization [19][20][21][22]. Catalysis of epoxy-anhydride reactions is often performed with Lewis base catalysts such as tertiary amines, amidines, quaternary onium salts, or metal salts.…”
Section: Accepted Manuscriptmentioning
confidence: 99%