Abstract

Desiccant composites were prepared from a polystyrene homopolymer (PS) and a high impact copolymer (HIPS). Five zeolites were used as adsorbents, which included the A and X types frequently used in industrial practice. Composites containing zeolites up to 50 vol% were homogenized in an internal mixer and then compression molded to 1 mm thick plates. The results proved that the water adsorption capacity of zeolites depends on the total volume of the pores, whereas the rate of adsorption on thermodynamics, on the equilibrium constant of adsorption. On the other hand, zeolite characteristics influence the moisture adsorption of the composites only marginally; adsorption capacity is determined by zeolite content, whereas the rate of adsorption is determined by the properties of the polymer. Composites prepared with X type zeolites have somewhat smaller water adsorption capacity than those containing their A type counterparts. The dispersion of the zeolite is good both in PS and in HIPS composites. Mechanical properties are excellent mainly because of the good interfacial adhesion between the components. Because of their larger surface energy, composites containing X type zeolites have larger viscosity and they reinforce the polymer more than A type desiccants. Matrix characteristics influence mainly application related properties; reinforcement and ductility is better in HIPS than in PS composites. POLYM. COMPOS., 35:2112–2120, 2014. © 2014 Society of Plastics Engineers

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.