2013
DOI: 10.4028/www.scientific.net/amr.634-638.3008
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis of Two Novolac Type Epoxy Resin Curing Agents and their Application

Abstract: Two Novolac Resins Were Synthesized by the Reaction between Bisphenol A and Benzaldehyde (bis-BENR) or Bisphenol A and P-hydroxybenzaldehyde (bis-PHNR). Fourier Transform Infrared Spectroscopy (FTIR) and Nuclear Magnetic Resonance (NMR) Were Applied to Characterize the Molecular Structure of Bis-BENR (or Bis-PHNR). then the Two Novolac Resins Were Used as Curing Agent for Bisphenol A Type Epoxy Resin (DGEBA). the Curing Reaction and Curing Kinetics Were Studied by Dynamic FTIR and Differential Scanning Calorim… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2022
2022
2022
2022

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 18 publications
0
2
0
Order By: Relevance
“…It can be seen from the figure that the characteristic peak of epoxy group (at 915 cm −1 ) of the EP system corresponding to the synthetic curing agent completely disappeared after curing for 6 h, indicating that the curing degree was relatively complete. 18 …”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…It can be seen from the figure that the characteristic peak of epoxy group (at 915 cm −1 ) of the EP system corresponding to the synthetic curing agent completely disappeared after curing for 6 h, indicating that the curing degree was relatively complete. 18 …”
Section: Resultsmentioning
confidence: 99%
“…It can be seen from the gure that the characteristic peak of epoxy group (at 915 cm À1 ) of the EP system corresponding to the synthetic curing agent completely disappeared aer curing for 6 h, indicating that the curing degree was relatively complete. 18 It is worth noting that aer curing the E-51/TLMPA mixture, no characteristic peak was found at 2500-2600 cm À1 , the common spectrum segment of the -SH group. 19 The strength of -SH group itself is weak and difficult to detect also due to the interference of conjugated double bonds or triple bonds in the system.…”
Section: Ftir Characterizationmentioning
confidence: 92%