Temperature dependence on free volume in cured natural rubber and styrene-butadiene rubber blends

A systematic study on the evolution of free volume as a function of the temperature in vulcanized at 433 K natural rubber (NR) and styrene butadiene rubber (SBR) in 25-75, 50-50, 75-25 NR-SBR (percent content of pure NR and SBR, respectively) blends was studied by positron annihilation lifetime spec...

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Autores principales: Mansilla, Marcela Angela, Marzocca, Angel José
Publicado: 2011
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_15393755_v83_n5_p_Salgueiro
http://hdl.handle.net/20.500.12110/paper_15393755_v83_n5_p_Salgueiro
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spelling paper:paper_15393755_v83_n5_p_Salgueiro2023-06-08T16:20:50Z Temperature dependence on free volume in cured natural rubber and styrene-butadiene rubber blends Mansilla, Marcela Angela Marzocca, Angel José Complex behavior Cross-link densities Lifetime data Linear functions Nanoholes Natural rubbers ortho-Positronium lifetime Positron annihilation lifetime spectroscopy State of cure Styrene butadiene rubber Sulfenamides Systematic study Temperature curves Temperature dependence Thermal expansion coefficients Butadiene Curing Differential scanning calorimetry Free volume Glass transition Positron annihilation spectroscopy Positrons Styrene Sulfur Thermal expansion Rubber A systematic study on the evolution of free volume as a function of the temperature in vulcanized at 433 K natural rubber (NR) and styrene butadiene rubber (SBR) in 25-75, 50-50, 75-25 NR-SBR (percent content of pure NR and SBR, respectively) blends was studied by positron annihilation lifetime spectroscopy. All samples were prepared with sulfur and TBBS (n-t-butyl-2-benzothiazole sulfenamide) as accelerator. The glass transition temperatures of the samples studied were determined by differential scanning calorimetry (DSC) and from lifetime data. In general, a sigmoidal-like complex behavior of the long-lived lifetime component, linked to the nanohole free volume, as a function of the temperature was found. For SBR, the slope of the ortho-positronium lifetime against temperature curves could be well-fitted using a linear function. For blends and also for NR, two different linear functions were necessary. This last behavior is explained in terms of the supercooled process involving a reconfiguration of the elastomeric chains. In the case of blends, the state of cure of NR and SBR in each NR-SBR sample was also taken into account in the discussion of the results obtained. Besides, thermal expansion coefficients of the free volumes in the transition and glassy region of all compounds were estimated. The differences observed in the values of this parameter are discussed by taking into account the morphology and formulation of each blend, the crosslink densities, and the role of the interphases formed between both NR and SBR elastomers. © 2011 American Physical Society. Fil:Mansilla, M.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Marzocca, A.J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2011 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_15393755_v83_n5_p_Salgueiro http://hdl.handle.net/20.500.12110/paper_15393755_v83_n5_p_Salgueiro
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Complex behavior
Cross-link densities
Lifetime data
Linear functions
Nanoholes
Natural rubbers
ortho-Positronium lifetime
Positron annihilation lifetime spectroscopy
State of cure
Styrene butadiene rubber
Sulfenamides
Systematic study
Temperature curves
Temperature dependence
Thermal expansion coefficients
Butadiene
Curing
Differential scanning calorimetry
Free volume
Glass transition
Positron annihilation spectroscopy
Positrons
Styrene
Sulfur
Thermal expansion
Rubber
spellingShingle Complex behavior
Cross-link densities
Lifetime data
Linear functions
Nanoholes
Natural rubbers
ortho-Positronium lifetime
Positron annihilation lifetime spectroscopy
State of cure
Styrene butadiene rubber
Sulfenamides
Systematic study
Temperature curves
Temperature dependence
Thermal expansion coefficients
Butadiene
Curing
Differential scanning calorimetry
Free volume
Glass transition
Positron annihilation spectroscopy
Positrons
Styrene
Sulfur
Thermal expansion
Rubber
Mansilla, Marcela Angela
Marzocca, Angel José
Temperature dependence on free volume in cured natural rubber and styrene-butadiene rubber blends
topic_facet Complex behavior
Cross-link densities
Lifetime data
Linear functions
Nanoholes
Natural rubbers
ortho-Positronium lifetime
Positron annihilation lifetime spectroscopy
State of cure
Styrene butadiene rubber
Sulfenamides
Systematic study
Temperature curves
Temperature dependence
Thermal expansion coefficients
Butadiene
Curing
Differential scanning calorimetry
Free volume
Glass transition
Positron annihilation spectroscopy
Positrons
Styrene
Sulfur
Thermal expansion
Rubber
description A systematic study on the evolution of free volume as a function of the temperature in vulcanized at 433 K natural rubber (NR) and styrene butadiene rubber (SBR) in 25-75, 50-50, 75-25 NR-SBR (percent content of pure NR and SBR, respectively) blends was studied by positron annihilation lifetime spectroscopy. All samples were prepared with sulfur and TBBS (n-t-butyl-2-benzothiazole sulfenamide) as accelerator. The glass transition temperatures of the samples studied were determined by differential scanning calorimetry (DSC) and from lifetime data. In general, a sigmoidal-like complex behavior of the long-lived lifetime component, linked to the nanohole free volume, as a function of the temperature was found. For SBR, the slope of the ortho-positronium lifetime against temperature curves could be well-fitted using a linear function. For blends and also for NR, two different linear functions were necessary. This last behavior is explained in terms of the supercooled process involving a reconfiguration of the elastomeric chains. In the case of blends, the state of cure of NR and SBR in each NR-SBR sample was also taken into account in the discussion of the results obtained. Besides, thermal expansion coefficients of the free volumes in the transition and glassy region of all compounds were estimated. The differences observed in the values of this parameter are discussed by taking into account the morphology and formulation of each blend, the crosslink densities, and the role of the interphases formed between both NR and SBR elastomers. © 2011 American Physical Society.
author Mansilla, Marcela Angela
Marzocca, Angel José
author_facet Mansilla, Marcela Angela
Marzocca, Angel José
author_sort Mansilla, Marcela Angela
title Temperature dependence on free volume in cured natural rubber and styrene-butadiene rubber blends
title_short Temperature dependence on free volume in cured natural rubber and styrene-butadiene rubber blends
title_full Temperature dependence on free volume in cured natural rubber and styrene-butadiene rubber blends
title_fullStr Temperature dependence on free volume in cured natural rubber and styrene-butadiene rubber blends
title_full_unstemmed Temperature dependence on free volume in cured natural rubber and styrene-butadiene rubber blends
title_sort temperature dependence on free volume in cured natural rubber and styrene-butadiene rubber blends
publishDate 2011
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_15393755_v83_n5_p_Salgueiro
http://hdl.handle.net/20.500.12110/paper_15393755_v83_n5_p_Salgueiro
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AT marzoccaangeljose temperaturedependenceonfreevolumeincurednaturalrubberandstyrenebutadienerubberblends
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