Journals / Turkish Journal of Chemistry / 2020 / Cilt: 44 - Sayı: 3

Improvement of the adhesion of conductive poly(m-toluidine) onto chemically reduced-wool fabrics

Pages
775–790
Publication Date
2022-11-01
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The performance ofPMT/wool composite was also examined in the electromagnetic shielding effectiveness (EMSE) measurements within 30MHz-3 GHz.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Wool has disulphide bonds containing-hydrophobic external keratin layers, which act as a barrier for themodification through coating with hydrophilic materials.
📊
Key Findings & Data:The effects of conditions, such as the composition of reduction-bath and types of dopants wereinvestigated, on the mass increase (%) and surface resistivity of the composite.
💡
Conclusion & Impact:The performance ofPMT/wool composite was also examined in the electromagnetic shielding effectiveness (EMSE) measurements within 30MHz-3 GHz.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Wool has disulphide bonds containing-hydrophobic external keratin layers, which act as a barrier for themodification through coating with hydrophilic materials. For that reason, in this work, to ensure a dense and homogenousconductive polymer coating onto the wool, the fabrics were subjected to the reduction process in the aqueous alkalinemedium containing agents that can attack these disulphide bonds. Then, one of the polyaniline derivatives, poly(mtoluidine) (PMT), was coated onto wool by in situ polymerization of m-toluidine sulphate using ammonium persulfate(APS) as an oxidant. The effects of conditions, such as the composition of reduction-bath and types of dopants wereinvestigated, on the mass increase (%) and surface resistivity of the composite. The reduction pretreatment of wool withsodium hydrosulphide significantly improved the coating density, conductivity, and colour shade of PMT on the surface,compared to an untreated one. The coating stability of PMT/wool composite was examined by rubbing test and detergentwashing, through surface resistivity measurements. The changes in structural and surface properties of wool fabricswere determined with ATR-FTIR, contact angle, and optical microscopic techniques, respectively. The performance ofPMT/wool composite was also examined in the electromagnetic shielding effectiveness (EMSE) measurements within 30MHz-3 GHz.

🔖

Cite This Article

ERDOĞAN, M. K., KARAKIŞLA, M., SAÇAK, M. (2022). Improvement of the adhesion of conductive poly(m-toluidine) onto chemically reduced-wool fabrics. Turkish Journal of Chemistry, Cilt: 44 - Sayı: 3, 775–790. https://ajindex.com/articles/601531

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (12)

  1. Maestá Bezerra F, García Carmona Ó, García Carmona C, Souza Plath AM, Lis M. Biofunctional wool using β - cyclodextrins as vehiculizer of citronella oil. Process Biochem 2019
  2. doi: 10.1016/j.procbio.2018.11.018 2. Wang Q, Li J, Bai Y, Lu X, Ding Y et al. Photodegradation of textile dye Rhodamine B over a novel biopolymer– metal complex wool-Pd/CdS photocatalysts under visible light irradiation. Journal of Photochemistry and Photobiology B: Biology 2013
  3. doi: 10.1016/j.jphotobiol.2013.07.007 3. Kantouch A-a, Abdel-Fattah S, Hebeish A. Manganese(IV)-Initiated Graftcopolymerization of Methyl Methacrylate on Wool Fibers. Polymer Journal 1972
  4. 3 (6): 675-680. doi: 10.1295/polymj.3.675 4. Shavandi A, Ali MA. Graft polymerization onto wool fibre for improved functionality. Progress in Organic Coatings 2019
  5. doi: 10.1016/j.porgcoat.2019.01.054 5. Misra BN, Mehta IK, Sharma RK. Grafting onto wool. Polymer Bulletin 1980
  6. 3 (1): 115-121. doi: 10.1007/BF00263214 6. Ranjbar-Mohammadi M, Arami M, Bahrami H, Mazaheri F, Mahmoodi NM. Grafting of chitosan as a biopolymer onto wool fabric using anhydride bridge and its antibacterial property. Colloids and Surfaces B: Biointerfaces 2010
  7. 76 (2): 397-403. doi: 10.1016/j.colsurfb.2009.11.014 7. Zhao W, Kong M, Feng C, Cheng X, Liu Y et al. Investigation of gelling behavior of thiolated chitosan in alkaline condition and its application in stent coating. Carbohydrate Polymers 2016
  8. doi: 10.1016/j.carbpol.2015.09.049 8. Vijayaraghavan R, Vedaraman N, Muralidharan C, Mandal AB, MacFarlane DR. Aqueous ionic liquid solutions as alternatives for sulphide-free leather processing. Green Chemistry 2015
  9. 17 (2): 1001-1007. doi: 10.1039/C4GC01476F 9. Matsuda H, Takahashi M, Shinoda K, Kikyotani S, Inagaki H. Process for producing reduced keratinous substances using urea or thiourea. 1979, Google Patents. 10. Wang K, Li R, Ma JH, Jian YK, Che JN. Extracting keratin from wool by using l-cysteine. Green Chemistry 2016
  10. 18 (2): 476-481. doi: 10.1039/C5GC01254F 11. Kuzuhara A, Hori T. Reduction mechanism of tioglycolic acid on keratin fibers using microspectrophotometry and FT-Raman spectroscopy. Polymer 2003
  11. 44 (26): 7963-7970. 12. Kakkar P, Madhan B, Shanmugam G. Extraction and characterization of keratin from bovine hoof: A potential material for biomedical applications. SpringerPlus 2014
  12. 3 (1): 596. doi: 10.1186/2193-1801-3-596 13. Zhang P, Zhang N, Wang Q, Wang P, Yuan J et al.