Study of the hygrothermal aging of a phenolic matrix and glass fiber composite

The hygrothermal-oxidative aging of a phenolic/short glass fiber composite was studied in a humid environment (100% relative humidity) for over a year at three temperatures: 50°C, 70°C, and 90°C. Wet aging of this composite is rarely studied in the literature due to the nature of its matrix. Indeed, phenolic resins are usually used to resist thermal stress at very high temperatures. Infrared spectroscopy by ATR mode, dynamic thermomechanical analyses, water sorption measurements and optical microscopy were used in a complementary way to monitor the influence of humidity, oxygen and temperature on the composite structure. From the first aging times, resin plasticizing and post-curing of resin are associated to cracks occurring from the resin/fiber interface, due to the hydration of the fibers which would be treated by silane-type coupling agent. Sub-crosslinking would be related to the presence of intermediate products such as amides, imides, or phenol groups in excess, strongly hydrophilic. Consequently, along with time, hydrolysis is accelerated. Moreover, the oxidation products revealed by FTIR analyses will favor interactions with water. The cracks are then deviated inwards the resin matrix.

Authors

Institutions

Publication Details

Journal
Journal of Composite Materials
Published
2025-03-29
DOI
https://doi.org/10.1177/00219983251331731
Citations
1
Primary Topic
Natural Fiber Reinforced Composites
Type
article
Field-Weighted Citation Impact
0.61
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Study of the hygrothermal aging of a phenolic matrix and glass fiber composite

Océane-Sophie Bérot, Bouchra Hassoune‐Rhabbour, Philippe Durand, Hélène Canot et al.
1 citations
Journal of Composite Materials
Natural Fiber Reinforced Composites
0.61
article

Study of the hygrothermal aging of a phenolic matrix and glass fiber composite

Océane-Sophie Bérot, Bouchra Hassoune‐Rhabbour, Philippe Durand, Hélène Canot, Valérie Nassiet, Hervé Acheritobehere, Caroline Laforet
article en
1 citations

Abstract

The hygrothermal-oxidative aging of a phenolic/short glass fiber composite was studied in a humid environment (100% relative humidity) for over a year at three temperatures: 50°C, 70°C, and 90°C. Wet aging of this composite is rarely studied in the literature due to the nature of its matrix. Indeed, phenolic resins are usually used to resist thermal stress at very high temperatures. Infrared spectroscopy by ATR mode, dynamic thermomechanical analyses, water sorption measurements and optical microscopy were used in a complementary way to monitor the influence of humidity, oxygen and temperature on the composite structure. From the first aging times, resin plasticizing and post-curing of resin are associated to cracks occurring from the resin/fiber interface, due to the hydration of the fibers which would be treated by silane-type coupling agent. Sub-crosslinking would be related to the presence of intermediate products such as amides, imides, or phenol groups in excess, strongly hydrophilic. Consequently, along with time, hydrolysis is accelerated. Moreover, the oxidation products revealed by FTIR analyses will favor interactions with water. The cracks are then deviated inwards the resin matrix.

Journal of Composite MaterialsVol. 59(20)
Conservatoire National des Arts et Métiers (FR), Université de Bretagne Sud (FR), Laboratoire Génie de Production (FR), Roxel (France) (FR)
Openalex Percentile: Top 38%
Natural Fiber Reinforced Composites
0.61
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.