Reprotonated polyanilines: The stability of conductivity at elevated temperature

Reprotonation of polyaniline base with various acids opens a way to conducting materials widely differing in physical properties. The thermal stability of the resulting polyaniline salts was tested by measurements of the conductivity at 125 °C for up to 500 h. Polyaniline sulfate was the most stable...

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Veröffentlicht in:Polymer degradation and stability 2014-04, Vol.102, p.67-73
Hauptverfasser: Stejskal, Jaroslav, Prokeš, Jan, Trchová, Miroslava
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container_title Polymer degradation and stability
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creator Stejskal, Jaroslav
Prokeš, Jan
Trchová, Miroslava
description Reprotonation of polyaniline base with various acids opens a way to conducting materials widely differing in physical properties. The thermal stability of the resulting polyaniline salts was tested by measurements of the conductivity at 125 °C for up to 500 h. Polyaniline sulfate was the most stable and its resistivity increased only by 3.6 times after that time. The stability differed considerably depending on the acid used for reprotonation. The room-temperature conductivity of polyaniline salt is determined by the strength of the acid and its ionic bond with the imine nitrogen in polyaniline. The thermal stability of conductivity, however, is controlled by the ability of the acid to constitute hydrogen bonds with the secondary amine nitrogens in polyaniline. For that reason, oxygen-containing counter-ions, such as sulfates or sulfonates, produce more stable salts with polyaniline, compared with polyaniline protonated with, e.g., hydrochloric acid. The presence of hydroxyl group in the counter-ions also enhances the thermal stability of the polyaniline salt. These conclusions are supported by the analysis of FTIR spectra.
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The thermal stability of the resulting polyaniline salts was tested by measurements of the conductivity at 125 °C for up to 500 h. Polyaniline sulfate was the most stable and its resistivity increased only by 3.6 times after that time. The stability differed considerably depending on the acid used for reprotonation. The room-temperature conductivity of polyaniline salt is determined by the strength of the acid and its ionic bond with the imine nitrogen in polyaniline. The thermal stability of conductivity, however, is controlled by the ability of the acid to constitute hydrogen bonds with the secondary amine nitrogens in polyaniline. For that reason, oxygen-containing counter-ions, such as sulfates or sulfonates, produce more stable salts with polyaniline, compared with polyaniline protonated with, e.g., hydrochloric acid. The presence of hydroxyl group in the counter-ions also enhances the thermal stability of the polyaniline salt. 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The thermal stability of the resulting polyaniline salts was tested by measurements of the conductivity at 125 °C for up to 500 h. Polyaniline sulfate was the most stable and its resistivity increased only by 3.6 times after that time. The stability differed considerably depending on the acid used for reprotonation. The room-temperature conductivity of polyaniline salt is determined by the strength of the acid and its ionic bond with the imine nitrogen in polyaniline. The thermal stability of conductivity, however, is controlled by the ability of the acid to constitute hydrogen bonds with the secondary amine nitrogens in polyaniline. For that reason, oxygen-containing counter-ions, such as sulfates or sulfonates, produce more stable salts with polyaniline, compared with polyaniline protonated with, e.g., hydrochloric acid. The presence of hydroxyl group in the counter-ions also enhances the thermal stability of the polyaniline salt. 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source Elsevier ScienceDirect Journals
subjects Ageing
Applied sciences
Conducting polymer
Conductivity
Degradation
Exact sciences and technology
High temperature
Hydrogen bonding
Hydroxyl groups
Physical properties
Polyaniline
Polyanilines
Polymer industry, paints, wood
Properties and testing
Stability
Sulfates
Sulfonates
Technology of polymers
Thermal stability
title Reprotonated polyanilines: The stability of conductivity at elevated temperature
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