Eco-friendly functionalization of hexagonal boron nitride nanosheets with carbon dots towards reinforcement of the protective performance of water-borne epoxy coatings. (16th March 2022)

• Record Type: Journal Article
• Authors: Yu, Yue; Cui, Mingjun; Zheng, Wenru; Zhao, Haichao
• Is Part Of: New journal of chemistry. Volume 46:Number 13(2022)
• Page Start: 6330
• Page End: 6342
• Publication Date: 2022-03-16
• Subjects: Chemistry -- Periodicals; Chimie -- Périodiques; 540
• DOI: 10.1039/d2nj00310d
• Languages: English
• ISSNs: 1144-0546

Abstract

Abstract : A h-BN@CDs/WEP coating shows superior corrosion protection under intact or damaged status owing to the improved barrier properties and interfacial bonding of the coating. Abstract : As a structural analogue of graphene, hexagonal boron nitride (h-BN) is receiving increased attention in the field of anticorrosive polymer coatings due to its electrical insulation and high barrier properties. However, the hydrophobicity of h-BN nanosheets makes them easily aggregate in water, thereby limiting their application in water-borne polymer coatings for corrosion protection. In this study, carbon dots (CDs) derived from citric acid are prepared as a dispersant for improving the dispersion of h-BN nanosheets in a water-borne epoxy (WEP) coating by taking advantage of the π–π interaction between h-BN and CDs. The possible reaction between oxygen functional groups on the CD surface and unreacted epoxy resin/curing agent could increase the compatibility and crosslinking density between h-BN and the WEP matrix, which in turn effectively reinforces the barrier effect of the composite coating. EIS results show that the impedance modulus of the h-BN@CDs/WEP coating is higher than 10 8 Ω cm 2 after 34 d of exposure in 3.5 wt% NaCl solution, nearly three orders of magnitude higher than those of pure WEP and h-BN/WEP (∼10 5 Ω cm 2 ). Additionally, salt spray and LEIS results reveal the superior corrosion protection performance of the h-BN@CDs/WEP coating even under damaged status.