Preparation of an Electrically Conductive Flexible Coating onto the Polyester Films from Wool Keratin Particles/Poly(ethylene glycol dimethacrylate)/Polyaniline for Soft Electrode Design


Tecer A.

7th Eurasia Biochemical Approaches & Technologies Congress (EBAT), Antalya, Türkiye, 6 - 09 Kasım 2025, ss.136, (Yayınlanmadı)

  • Yayın Türü: Bildiri / Yayınlanmadı
  • Basıldığı Şehir: Antalya
  • Basıldığı Ülke: Türkiye
  • Sayfa Sayıları: ss.136
  • Yozgat Bozok Üniversitesi Adresli: Evet

Özet

Electrically conductive and flexible coating materials are of great importance, particularly in

electrochemical applications such as biosensor design, heavy metal ion detection, and the sensing of

biomacromolecules. In the development of such materials, the use of sustainable biopolymers and

environmentally friendly approaches has received significant attention.1 Keratin, a natural protein

derived from waste wool, stands out due to its biocompatibility, functional groups, and environmental

sustainability.2 Polyaniline (PAn), on the other hand, is one of the most widely studied conducting

polymers owing to its tunable oxidation states, high electrical conductivity, and facile synthesis.

Furthermore, gel-like network structures such as PEGDMA provide compatibility with organic–

inorganic hybrid systems, offering both flexibility and functional coating capabilities. Previous studies

have reported that the polymerization conditions of aniline (Ani/APS molar ratio, reagent volumes,

and reaction time) have critical effects on PAn yield, surface morphology, and conductivity. In this

context, the development of environmentally friendly, flexible, and conductive composite materials

represents a significant research field for biosensor electrode design. In this study, electrically

conductive and flexible electrode materials were prepared by in situ surface polymerization of aniline

on commercial polyester films. During synthesis, keratin particles (KerSH) derived from sustainable

wool waste were immobilized onto the polyester surface through a PEGDMA gel-like paste. This was

achieved via a thiol-ene “click” reaction between PEGDMA and thioglycolic acid (TGA), resulting in the

encapsulation of KerSH particles within the PEGDMA network. Subsequently, aniline monomers were

polymerized in the presence of ammonium persulfate (APS) oxidant on the gel coating, leading to the

formation of a conductive polyaniline (PAn) layer. The effects of polymerization parameters (reagent

volumes and Ani/APS molar ratio) on the PAn content (%) and surface resistivity were systematically

investigated. The prepared composite films were characterized in terms of functional groups by ATR-

FTIR spectroscopy, morphology by optical microscopy, and surface wettability by contact angle and

wetting time measurements. The results demonstrated that the developed materials exhibited high

electrical conductivity along with chemically active surface functionalities, making them promising

candidates for application in biosensor electrode design.