High impact strength of aliphatic polyketone/polyamide 6 blends induced by a chemical reaction
Source abstract
Abstract
Compatibility and physical properties of aliphatic polyketon (PK)/polyamide 6 (PA6) blend were investigated. The PK and PA6 showed high adhesion strength and thus impact strength of PK/PA6 blends was very high. It was observed that PK-PA6 copolymers are formed by a chemical reaction between the two polymers and the copolymers act as a reactive compatibilizer in the PK/PA6 blends. The presence of the PK-PA6 copolymer was confirmed by FTIR analysis. The adhesion strength between PK and PA6 was very high compared to a typical incompatible polymer pair. PA6 investigated herein has two end groups, NH 2 and carboxylic acid. We also adopted end-capped PA6 that has two carboxylic acid end groups. The adhesion strength and impact strength of the PK/end-capped PA6 blends was much lower than that of PK/PA6 blends. More importantly, the PK-PA6 copolymer was not formed in the PK/end-capped PA6 blends. Thus, it was concluded that the chemical reaction occurs between the carbonyl of PK and the primary amine end group of PA6. Due to the high impact strength of PK/PA6 blends, possible applications could be automotive parts where higher impact strength is required.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Polymer crystallization and properties · Polymer Nanocomposites and Properties · Synthesis and properties of polymers
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Division of Advanced Materials Science and Engineering, Kongju National University, Cheonan, S. Korea
Department Aero-Materials Engineering, Jungwon University, Goesan-gun, Republic of Korea
Department of Chemistry, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea
POK Business Division, Hyosung Chemical, Seoul, Republic of Korea
R&D Center of Green Environment Corporation, Cheonan, S. Korea
Funding
Kongju National University
References (29)
Show source-provided references
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