Epoxy Resins and Composites II
DOI: 10.1007/bfb0017916
|View full text |Cite
|
Sign up to set email alerts
|

Kinetics, thermodynamics and mechanism of reactions of epoxy oligomers with amines

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

7
149
0
2

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations
Cited by 369 publications
(158 citation statements)
references
References 49 publications
7
149
0
2
Order By: Relevance
“…In case of the 50% WS sample, a higher intensity of the absorbance peak (at 3500 cm -1 ) may be observed than for unmodified epoxy resin [26,27]. This fact may be attributed both to the presence of the organic filler in the composite material, as well as the effect catalytic reaction of the curing process caused by the presence of additional -OH groups originating from the filler [28,29]. Detailed description of all observed at FT-IR spectra peaks was presented in Table 1.…”
Section: Evaluation Of Composite Materials' Properties and Structurementioning
confidence: 93%
“…In case of the 50% WS sample, a higher intensity of the absorbance peak (at 3500 cm -1 ) may be observed than for unmodified epoxy resin [26,27]. This fact may be attributed both to the presence of the organic filler in the composite material, as well as the effect catalytic reaction of the curing process caused by the presence of additional -OH groups originating from the filler [28,29]. Detailed description of all observed at FT-IR spectra peaks was presented in Table 1.…”
Section: Evaluation Of Composite Materials' Properties and Structurementioning
confidence: 93%
“…This remake indicates that the curing reaction is autocatalytic, and within the experiment temperature range, the temperature will little affect the autocatalytic reaction mechanism. As illustrated in Scheme 3, the autocatalytic reaction mechanism results from the hydroxyl groups generated from the epoxy-amine ring-opening reaction that can catalyze the further curing reaction via a trimolecular transition state [34,35]. …”
Section: Figmentioning
confidence: 99%
“…The addition of CNTs [19,20,31] and EG [24] decreased the "H of epoxy, whereas CNF had no pronounced effect on the heat of the TGDDM/DDS cure reaction [32] and silanized and polyaniline modified CNFs increased the "H of epoxy [33,34]. It is believed that the addition of hydroxyl-containing compounds (water, alcohols, phenols, acids) considerably promoted the interaction of epoxy compounds with amines and other nucleophilic reagents [35]. In this case, the epoxy ring carbon atom became more sensitive to nucleophilic attack.…”
Section: Effects Of Gos On the Cure Reactionmentioning
confidence: 99%