Abstract

Organomodified clays are known to be effective in polymer blend compatibilization if located preferentially at the domain interfaces, but little is known regarding the origin of their localization. In this study, we investigate the effect of organomodifier, clay loading, and shear environment on the compatibilization extent in nonreactive polyethylene (LDPE)/poly(ethylene oxide) (PEO) and reactive maleic anhydride functional polyethylene (PE-g-MA)/PEO polymer blends. We pose important questions: If clay is to compatibilize blends by interfacial localization, how does organomodifier affect its localization? How does an increase in clay loading affect the shape and elasticity of the interface? What is the shear intensity needed to overcome the equilibrium distribution of clays and delaminate it from the interface? We utilize laser scanning confocal microscopy and 3D image analysis to calculate characteristic phase size and gain unique insights into the connection between the clay loading and the interfacial...

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