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dc.contributor.authorSeah, Geok Leng.
dc.description.abstractAnti-biofouling aims to prevent the acculumulation of biological organisms like proteins and micro-organisms on surfaces. This can be achieved by applying anti-biological and fouling release non-toxic polymeric coatings on surfaces. Conventional production of polymer composites is a time consuming process which involves a long thermal curing step of the monomers into thermosets. An attractive cost saving and environmentally friendly alternative is to perform curing via UV radiation. It shortens the curing time greatly, lowers the curing temperature and requires little or no solvent. Thus, it is increasingly popular in the coating and microelectronic industries. Acrylates and other radical initiated monomers are widely studied and used in industry. However, they are highly sensitive to oxygen and have poor adhesion strength on many surfaces, making them poor coatings. By contrary, epoxides are more stable in oxygen and have good adhesion properties, establishing them as good coatings for many surfaces. Unfortunately, they are not as well studied and hence not widely used. It is desired to create an IPN of both epoxides and acrylates to retain the advantages of the individual polymers while increasing the hardness, impact strength and chemical resistance to produce a good anti-biofouling coating. Nanofillers are commonly added into polymer matrix to improve various properties of the materials. Hence, nanocomposites of TMPT(EO)A added with different nanofillers were UV-cured and studied kinetically. DPC was used to carry out the curing with the analysis of curing kinetics and photoreactivity simultaneously. Surface energy, tensile strength and hardness of the IPNs were analyzed via static water contact angle measurement, tensile test and Vicker micro hardness test. In this study, TMPTA, TMPT(EO)A, PEGDA, TPGDA, CN8003, CN104 and Epolam 5015 were used in the investigation of the formation of simultaneous IPNs with TMPT(EO)A, PEGDA and TPGDA as the most reactive monomers among the seven monomers and oligomers. The effects of composition of individual monomers and temperature were investigated under optimum photoinitiator concentration. The highest percentage conversion and highest rate of reaction was when the experiment was conducted at 70 ˚C with the highest acrylates proportion. The activation energies of the IPNs were found to be either between or lower than that of the monomers. IPNs containing CN8003 were suitable for fouling release purposes due to their low elastic modulus and surface energy. Its flexibility allows it to be an inner coating of the anti-biofouling system. IPNs containing TMPT(EO)A had high surface energy, tensile strength, elastic modulus and hardness, making it a good candidate as an anti-fouling resistive outer layer. Unmodified nanoclay-TMPT(EO)A nanocomposites had the highest photoreactivity and percentage conversion at 1 wt% unmodified nanoclay.en_US
dc.format.extent82 p.en_US
dc.subjectDRNTU::Engineering::Materials::Nanostructured materialsen_US
dc.subjectDRNTU::Science::Chemistry::Organic chemistry::Polymersen_US
dc.subjectDRNTU::Engineering::Materials::Composite materialsen_US
dc.subjectDRNTU::Engineering::Materials::Functional materialsen_US
dc.titleDevelopment of Interpenetrating Network (IPN) hybrid composite for thin film protectionen_US
dc.contributor.supervisorLu Xuehongen_US
dc.contributor.supervisorMarc Jean Medard Abadieen_US
dc.contributor.schoolSchool of Materials Science & Engineeringen_US
dc.description.degreeMaster of Engineering (MSE)en_US
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