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Morphology and chain mobility of reactive blend nanocomposites of PP‐EVA/Clay
Authors:José M Mata‐Padilla  Francisco J Medellín‐Rodríguez  Carlos A Ávila‐Orta  Eduardo Ramírez‐Vargas  Gregorio Cadenas‐Pliego  Mario Valera‐Zaragoza  Sofía M Vega‐Díaz
Affiliation:1. Centro de Investigación y Estudios de Posgrado, Facultad de Ciencias Químicas, Universidad Autónoma de San Luis Potosí, Av. Dr. Manuel Nava 6, Zona Universitaria, San Luis Potosí, México;2. Centro de Investigación en Química Aplicada (CIQA), Blvd. Enrique Reyna Hermosillo 140, Saltillo, Coahuila, México;3. Universidad del Papaloapan, Tuxtepec, Oaxaca, México;4. Research Center for Exotic Nanocarbons (JST), Shinshu University, Japan
Abstract:Polypropylene (PP)‐ethylene vinyl acetate (EVA)/clay nanocomposites were prepared via reactive blending using dicumyl peroxide (DCP) as an initiator with the goal of enhancing the interaction between both phases and modified nanoclay. The effect of the reactive blending and clay incorporation strategies (direct and masterbatch) on the blend and nanostructure morphology, and chain mobility of nanocomposites were studied. The chemical analysis showed the chemical bonding of PP‐EVA, which helped to enhance the interaction in the nanocomposites. The nanocomposites obtained from the direct clay strategy presented a co‐continuous morphology of bordering intercalated and agglomerated nanoclay sheets, while the nanocomposites obtained from the masterbatch strategy showed that blend morphology change from droplet to co‐continuous with the increase of EVA concentration, with intercalated/exfoliated nanoclay sheets located in the EVA domains and at the interface. The dynamic mechanical and creep‐recovery results showed different behavior for the both strategies in terms of chain mobility and relaxation. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40897.
Keywords:polyolefins  elastomers  crosslinking  clay  nanostructured polymers
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