Polyacetylene Prepared by Chemical Dehydration of Poly(Vinyl Alcohol)

Recently, polyacetylene (PA) has been receiving renewed scientific attention due to its electrical properties, potentially useful for energy applications (e.g., fabrication of electrodes for rechargeable batteries and supercapacitors), and unique functional characteristics (e.g., gas trap, oxygen scavenger, EMI shielding, etc.). This chemical compound can be obtained in the form of polyacetylene–PVOH copolymers simply through the chemical dehydration of poly(vinyl alcohol) (PVOH), which is a very common type of polymer, widely used in packaging and other technological areas. This very inexpensive chemical reaction for the large-scale synthesis of PA/polyvinylenes is investigated by reacting PVOH with sulfuric acid at room temperature. In this process, PVOH, shaped in the form of a film, is dipped in sulfuric acid (i.e., H2SO4 at 95%–97%) and, after complete chemical dehydration, it is mechanically removed from the liquid phase by using a nylon sieve. The reduction process leads to a substantial PVOH film conversion into PA, as demonstrated by infrared spectroscopy (ATR mode). Indeed, the ATR spectrum of the reaction product includes all the characteristic absorption bands of PA. The reaction product is also characterized through the use of UV–Vis spectroscopy in order to evidence the presence in the structure of conjugated carbon–carbon double bonds of various lengths. Differential scanning calorimetry (DSC) and thermogravimetric analysis are used to investigate the PA solid-state cis–trans isomerization and thermal stability in air and nitrogen, respectively. XRD is used to verify the polymer amorphous nature.

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Publication Details

Journal
Coatings
Published
2024-09-20
DOI
https://doi.org/10.3390/coatings14091216
Citations
1
Primary Topic
Polydiacetylene-based materials and applications
Type
article
Field-Weighted Citation Impact
0.25
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article

Polyacetylene Prepared by Chemical Dehydration of Poly(Vinyl Alcohol)

G. Carotenuto, L. Nicolais
1 citations
Coatings
Polydiacetylene-based materials and applications
0.25
article

Polyacetylene Prepared by Chemical Dehydration of Poly(Vinyl Alcohol)

G. Carotenuto, L. Nicolais
article en
1 citations

Abstract

Recently, polyacetylene (PA) has been receiving renewed scientific attention due to its electrical properties, potentially useful for energy applications (e.g., fabrication of electrodes for rechargeable batteries and supercapacitors), and unique functional characteristics (e.g., gas trap, oxygen scavenger, EMI shielding, etc.). This chemical compound can be obtained in the form of polyacetylene–PVOH copolymers simply through the chemical dehydration of poly(vinyl alcohol) (PVOH), which is a very common type of polymer, widely used in packaging and other technological areas. This very inexpensive chemical reaction for the large-scale synthesis of PA/polyvinylenes is investigated by reacting PVOH with sulfuric acid at room temperature. In this process, PVOH, shaped in the form of a film, is dipped in sulfuric acid (i.e., H2SO4 at 95%–97%) and, after complete chemical dehydration, it is mechanically removed from the liquid phase by using a nylon sieve. The reduction process leads to a substantial PVOH film conversion into PA, as demonstrated by infrared spectroscopy (ATR mode). Indeed, the ATR spectrum of the reaction product includes all the characteristic absorption bands of PA. The reaction product is also characterized through the use of UV–Vis spectroscopy in order to evidence the presence in the structure of conjugated carbon–carbon double bonds of various lengths. Differential scanning calorimetry (DSC) and thermogravimetric analysis are used to investigate the PA solid-state cis–trans isomerization and thermal stability in air and nitrogen, respectively. XRD is used to verify the polymer amorphous nature.

CoatingsVol. 14(9)
Federico II University Hospital (IT), National Research Council (IT), Institute of Polymers, Composites and Biomaterials (IT), University of Naples Federico II (IT)
Openalex Percentile: Top 48%
Polydiacetylene-based materials and applications
0.25
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