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Epoxy acrylate which is commercially utilized for UV curable coatings although has excellent adhesion, flexibility, hardness and chemical resistance, they lack in antimicrobial properties. Citric acid (CA) is economical as well as a bio-based compound which possess an antimicrobial activity. So, the purpose of this research investigation is the preparation of CA-based oligomer which can be further incorporated with epoxy acrylate and tri (propylene glycol) Diacrylate (TPGDA) to form uv curable coating and the study of its antimicrobial property.

A UV-curable unsaturated oligomer (CUV) was synthesized from CA and glycidyl methacrylate (GMA). The chemical structure of CUV was confirmed by FTIR, ¹H NMR, GPC, hydroxyl value, acid value and iodine value. Further, CUV was assimilated as an antimicrobial as well as crosslinking agent to copolymerize with epoxy acrylate oligomer and a series of UV-cured antimicrobial coatings were concocted by employing UV-curing machine. The consequence of varying the fraction of CUV on the mechanical, chemical, thermal and antimicrobial properties of UV-cured wood coatings was explored.

Results exhibited good mechanical, chemical and thermal properties. In addition, it was perceived that the zone of inhibition against S. aureus got enlarged with increasing content of CUV in the coating formulation.

The synthesized bio-based CUV reveals an extensive potential to ameliorate the antimicrobial properties of UV-curable coatings.

The purpose of this study is to synthesize structurally different phenalkamines based on cardanol, a renewable material obtained from cashew nut shell liquid, and to evaluate their effect on performance properties of the coatings.

For this purpose, the Mannich reaction between cardanol, formaldehyde and various diamines such as diaminodiphenyl methane (DDM), hexamethylene diamine, Jeffamine D400 and Jeffamine T403 were carried out to produce novel phenalkamines. Resultant phenalkamines were used as curing agents for commercial DGEBPA epoxy resin and were evaluated for performance properties.

The mechanical, optical, chemical, thermal and anticorrosive properties were evaluated and compared with those of commercial phenalkamine AG141. It was observed that anticorrosive properties evaluated using a salt spray test and electrochemical impedance spectroscopy revealed significant improvement in anticorrosive performance of coatings cured with synthesized phenalkamines based on DDM and T403 as compared to the coatings based on commercial phenalkamine AG141.

To obtain optimum performance properties of the coatings, a combination of phenalkamines can be used.

Curing time and gel times of all the phenalkamines can be further studied under wet and humid conditions. In addition, the variation in coating properties under humid conditions can be investigated.

In this study, newer phenalkamines were synthesized and used as curing agents for epoxy coatings. So far, there have been no reports indicating the synthesis and application of phenalkamines based on polyetheramines, namely, Jeffamine D400 and Jeffamine T403, in coating applications.

This paper aims to prepare acrylic functional ricinoleic acid monomer and incorporate it in conventional miniemulsion polymerization. Subsequently, paints were formulated to study the variation in final coating properties.

Synthesis process involved the esterification of ricinoleic acid with 2-hydroxy methyl methacrylate in the presence of FASCAT-4100 catalyst. The final product of the reaction, methacrylated ricinoleic acid (MRA), was confirmed using Fourier-transform infrared spectroscopy and ¹H-nuclear magnetic resonance spectroscopy and determining acid and iodine value. Further, MRA was incorporated in various concentrations (1, 2 and 3 Wt.%) along with methyl acrylate and butyl acrylate in conventional miniemulsion polymerization and paints were formulated thereof.

It was observed that with the addition of MRA monomer, flexibility of emulsion films increased as indicated by glass transition temperature and elongation value (percentage). Moreover, with the addition of MRA monomer, improvement in mechanical and chemical properties of the coatings was observed.

Even a low concentration MRA monomer (as low as 3 per cent) caused a significant reduction in the glass transition temperature of emulsion films. Thus, it can be efficiently used in applications such as adhesives and elastomeric coatings.

The acrylic functional monomer derived from ricinoleic acid is unique and not yet incorporated in miniemulsion polymerization. The synthesized monomer can be used in coatings where low Tg emulsions are required.