Silica/clay organo-heterostructures to promote polyethylene–clay nanocomposites by in situ polymerization
Author
dc.contributor.author
Zapata, Paula A.
Author
dc.contributor.author
Belver, Carolina
es_CL
Author
dc.contributor.author
Quijada Abarca, Juan
es_CL
Author
dc.contributor.author
Aranda, Pilar
es_CL
Author
dc.contributor.author
Ruiz Hitzky, Eduardo
es_CL
Admission date
dc.date.accessioned
2014-03-14T18:38:18Z
Available date
dc.date.available
2014-03-14T18:38:18Z
Publication date
dc.date.issued
2013
Cita de ítem
dc.identifier.citation
Applied Catalysis A: General 453 (2013) 142– 150
en_US
Identifier
dc.identifier.other
doi 10.1016/j.apcata.2012.12.012
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/126460
General note
dc.description
Artículo de publicación ISI
en_US
Abstract
dc.description.abstract
Two clay organo-heterostructures have been prepared and employed as fillers and catalyst supports for
the development of polyethylene–clay nanocomposites. The new silica–clay organo-heterostructures
have been obtained from two organoclays modified with tetramethoxysilane. In contrast to related
heterostructures reported previously the organic moieties are not removed by heating and their presence
intends to confer hydrophobicity to the interlayer region of the clay, even after delamination by
hydrolysis-polymerization of the alkoxysilane takes place. These organo-heterostructures were used
for preparing clay–polyethylene nanocomposites by in situ polymerizations in which the organoheterostructures
were added together with the metallocene catalyst, and by using the silica–clay as
support for the metallocene catalysts. The polymers formed when the organo-heterostructures were
used as support for the catalyst have higher molecular weights than the standard polyethylene formed
under homogeneous conditions. Moreover, the presence of the inorganic silica network developed in the
interlayer region of the organoclay favours the existence of a larger organophilic region in which it is
possible to accommodate both the catalyst and the monomer, and hence when the polymer grows in this
environment it can assist in the exfoliation of the clay layers inside the polyethylene matrix. The polymer
particle morphology improved with the presence of the clay in the polymerization. The molecular weight
for support systems presented an increasing ca. 40% compared to neat PE, and by TEM it was found that
the clay layers were well dispersed in the PE matrix.