Solvent-free encapsulation of curing agents for high performing one-component epoxy adhesives

Authors
Jee, Sung MinAhn, Cheol-HeePark, Jong HyukKim, Tae AnnPark, Min
Issue Date
2020-12-01
Publisher
ELSEVIER SCI LTD
Citation
COMPOSITES PART B-ENGINEERING, v.202
Abstract
One-component epoxy adhesives, in which the epoxy resin and curing agent are premixed, have many commercial advantages including reduced working time and stable performance. However, these adhesives suffer from a short shelf life even at room temperature. Here, core-shell structured curing agents were prepared via a dry particle coating (DPC) process that improved the storage stability of one-component epoxy adhesives. The DPC process is a simple, economic, and solvent-free method to fabricate core-shell structured materials using mechanical forces. Graphene nanoplatelets (GNPs) were used as encapsulating materials due to their high thermal conductivity and large surface areas. With the GNP-encapsulated curing agents, a one-component epoxy adhesive displayed significantly enhanced storage stability while maintaining its fast curing behavior. In particular, the pot life of the adhesive increased to 60 days, which is over two-times longer than that of a pristine epoxy adhesive. The curing temperature increased by up to 5.6 degrees C, which is a smaller increase than that observed when non-thermally conductive materials were used for encapsulation. Furthermore, the GNPs provided reinforcement in the cured epoxy adhesive, thereby improving the lap shear strength by 20-30%.
Keywords
NANOCOMPOSITES; COMPOSITES; MICROENCAPSULATION; STRENGTH; FRACTURE; NANOCOMPOSITES; COMPOSITES; MICROENCAPSULATION; STRENGTH; FRACTURE; Thermosetting resin; Cure behavior; Mechanical properties; Thermal analysis
ISSN
1359-8368
URI
https://pubs.kist.re.kr/handle/201004/117697
DOI
10.1016/j.compositesb.2020.108438
Appears in Collections:
KIST Article > 2020
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE