Pilar Posadas

Dr. Pilar Posadas

CSIC, Instituto de Ciencia y Tecnología de Polímeros, E-28006 Madrid, Spain
orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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15 April 2010 in Macromolecules
Verified
Journal Article
Closed access
Juan Lopez ValentinJuan Lopez Valentin
Juan Lopez Valentin
Pilar PosadasPilar Posadas
Pilar Posadas
AFA. Fernández-Torres
A. Fernández-Torres
MMM. A. Malmierca
M. A. Malmierca
LGL. González
L. González
KSKay Saalwachter
Kay Saalwachter

18 August 2014 in Macromolecules
Verified
Journal Article
Open access
MMM. A. Malmierca
M. A. Malmierca
Antonio González-JiménezAntonio González-Jiménez
Antonio González-Jiménez
IMI. Mora-Barrantes
I. Mora-Barrantes
Pilar PosadasPilar Posadas
Pilar Posadas
ARA. Rodríguez
A. Rodríguez
Juan Lopez ValentinJuan Lopez Valentin
Juan Lopez Valentin
The network structure and chain dynamics of ionic elastomers based on carboxylated nitrile rubber (XNBR) cross-linked with different content of magnesium oxide (MgO) have been studied by different low-field time-domain NMR experiments. Ionic contacts created during the vulcanization tend to aggregate trapping some polymer segments that show restricted mobility as it was quantified by analyses of refocused free induction decays. Increasing the MgO content above the stoichiometric fraction has no effect on the amount of trapped polymer segments, but it increases the network cross-link density as measured by multiple-quantum (MQ) NMR experiments. The central finding of this work is that MgO addition above the stoichiometric content enhances the mechanical properties by creating a larger number of smaller ionic clusters, which act as dynamic cross-links, but are not readily seen by other techniques. Changes in the network structure and morphology of segregated thermolabile ionic domains have an impact on the ionic rearrangement dynamics and, in consequence, on the thermoplastic behavior of these materials at elevated temperatures.

1 May 2007 in Applied Clay Science
Verified
Journal Article
Closed access
Juan Lopez ValentinJuan Lopez Valentin
Juan Lopez Valentin
Miguel Angel Lopez-ManchadoMiguel Angel Lopez-Manchado
Miguel Angel Lopez-Manchado
ARA. Rodríguez
A. Rodríguez
Pilar PosadasPilar Posadas
Pilar Posadas
LIL. Ibarra
L. Ibarra

1 June 2006 in Journal of Colloid and Interface Science
Verified
Journal Article
Closed access
Juan Lopez ValentinJuan Lopez Valentin
Juan Lopez Valentin
Miguel Angel Lopez-ManchadoMiguel Angel Lopez-Manchado
Miguel Angel Lopez-Manchado
Pilar PosadasPilar Posadas
Pilar Posadas
ARA. Rodríguez
A. Rodríguez
Angel Marcos-FernandezAngel Marcos-Fernandez
Angel Marcos-Fernandez
LIL. Ibarra
L. Ibarra

1 June 2020 in Polymer
Verified
Journal Article
Closed access
Pilar Bernal OrtegaPilar Bernal Ortega
Pilar Bernal Ortega
MBM. Mar Bernal
M. Mar Bernal
Antonio González-JiménezAntonio González-Jiménez
Antonio González-Jiménez
Pilar PosadasPilar Posadas
Pilar Posadas
Rodrigo NavarroRodrigo Navarro
Rodrigo Navarro
JVJuan L. Valentín
Juan L. Valentín

23 March 2017 in Soft Matter
Verified
Journal Article
Closed access
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Antonio González-JiménezAntonio González-Jiménez
Antonio González-Jiménez
MMMarta A. Malmierca
Marta A. Malmierca
Pilar Bernal OrtegaPilar Bernal Ortega
Pilar Bernal Ortega
Pilar PosadasPilar Posadas
Pilar Posadas
RPRoberto Pérez-Aparicio
Roberto Pérez-Aparicio
Juan Lopez ValentinJuan Lopez Valentin
Juan Lopez Valentin
Shape-memory elastomers based on a commercial rubber cross-linked by both ionic and covalent bonds have been developed. The elastomeric matrix was a carboxylated nitrile rubber (XNBR) vulcanized with magnesium oxide (MgO) providing ionic interactions that form hierarchical structures. The so-named ionic transition is used as the unique thermal transition responsible for the shape-memory effect (SME) in these elastomers. These ionic interactions fix the temporary shape due to their behavior as dynamic cross-links with temperature changes. Covalent cross-links were incorporated with the addition of different proportions of dicumyl peroxide (DCP) to the ionic elastomer to establish and recover the permanent shape. In this article, the SME was modulated by modifying the degree of covalent cross-linking, while keeping the ionic contribution constant. In addition, different programming parameters, such as deformation temperature, heating/cooling rate, loading/unloading rate and percentage of tensile strain, were evaluated for their effects on shape-memory behavior.