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dc.contributor.authorPlanellas Oates, Marc
dc.contributor.authorSacristan, Matias
dc.contributor.authorRey, Lorena
dc.contributor.authorOlmo Osuna, Cristian
dc.contributor.authorAymami Bofarull, Juan
dc.contributor.authorCasas Becerra, María Teresa
dc.contributor.authorValle Mendoza, Luis Javier del
dc.contributor.authorFranco García, María Lourdes
dc.contributor.authorPuiggalí Bellalta, Jordi
dc.contributor.otherUniversitat Politècnica de Catalunya. Departament d'Enginyeria Química
dc.date.accessioned2014-05-15T07:14:40Z
dc.date.created2014-07
dc.date.issued2014-07
dc.identifier.citationPlanellas, M. [et al.]. Micro-molding with ultrasonic vibration energy: New method to disperse nanoclays in polymer matrices. "Ultrasonics sonochemistry", Juliol 2014, vol. 21, núm. 4, p. 1557-1569.
dc.identifier.issn1350-4177
dc.identifier.urihttp://hdl.handle.net/2117/22993
dc.description.abstractUltrasound technology was proved as an efficient processing technique to obtain micro-molded specimens of polylactide (PLA) and polybutylene succinate (PBS), which were selected as examples of biodegradable polyesters widely employed in commodity and specialty applications. Operational parameters such as amplitude, molding force and processing time were successfully optimized to prepare samples with a decrease in the number average molecular weight lower than 6%. Ultrasonic waves also seemed an ideal energy source to provide effective disaggregation of clay silicate layers, and therefore exfoliated nanocomposites. X-ray diffraction patterns of nanocomposites prepared by direct micro-molding of PLA or PBS powder mixtures with natural montmorillonite or different organo-modified clays showed the disappearance of the 0 0 1 silicate reflection for specimens having up to 6 wt.% clay content. All electron micrographs revealed relatively homogeneous dispersion and sheet nanostructures oriented in the direction of the melt flow. Incorporation of clay particles during processing had practically no influence on PLA characteristics but enhanced PBS degradation when an organo-modifier was employed. This was in agreement with thermal stability data deduced from thermogravimetric analysis. Cold crystallization experiments directly performed on micro-molded PLA specimens pointed to a complex influence of clay particles reflected by the increase or decrease of the overall non-isothermal crystallization rate when compared to the neat polymer. In all cases, the addition of clay led to a clear decrease in the Avrami exponent.
dc.format.extent13 p.
dc.language.isoeng
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Spain
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.subjectÀrees temàtiques de la UPC::Enginyeria química
dc.subject.lcshPolymers
dc.subject.lcshNanocomposites (Materials)
dc.subject.otherCold crystallization
dc.subject.otherExfoliated structures
dc.subject.otherMicro-molding
dc.subject.otherNanocomposites
dc.subject.otherPolybutylene succinate
dc.subject.otherPolylactide
dc.titleMicro-molding with ultrasonic vibration energy: New method to disperse nanoclays in polymer matrices
dc.typeArticle
dc.subject.lemacPolímers
dc.subject.lemacNanocompòsits (Materials)
dc.contributor.groupUniversitat Politècnica de Catalunya. MACROM - Cristal·lografia, Estructura i Funció de Macromolècules Biològiques
dc.contributor.groupUniversitat Politècnica de Catalunya. PSEP - Polimers Sintètics: Estructura i Propietats. Polimers Biodegradables
dc.identifier.doi10.1016/j.ultsonch.2013.12.027
dc.description.peerreviewedPeer Reviewed
dc.relation.publisherversionhttp://www.sciencedirect.com/science/article/pii/S1350417714000030#
dc.rights.accessRestricted access - publisher's policy
local.identifier.drac14126261
dc.description.versionPostprint (published version)
dc.date.lift10000-01-01
local.citation.authorPlanellas, M.; Sacristan, M.; Rey, L.; Olmo, C.; Aymami, J.; Casas, M.; del Valle, LJ.; Franco, M.; Puiggali, J.
local.citation.publicationNameUltrasonics sonochemistry
local.citation.volume21
local.citation.number4
local.citation.startingPage1557
local.citation.endingPage1569


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