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Chemical Fingerprinting of Polymers Using Electron Energy-Loss Spectroscopy
[Image: see text] Electron energy-loss spectroscopy (EELS) is becoming an important tool in the characterization of polymeric materials. The sensitivity of EELS to changes in the chemical structure of polymeric materials dictates its applicability. In particular, it is important for compositional an...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459415/ https://www.ncbi.nlm.nih.gov/pubmed/34568672 http://dx.doi.org/10.1021/acsomega.1c02939 |
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author | Pal, Ruchi Bourgeois, Laure Weyland, Matthew Sikder, Arun K. Saito, Kei Funston, Alison M. Bellare, Jayesh R. |
author_facet | Pal, Ruchi Bourgeois, Laure Weyland, Matthew Sikder, Arun K. Saito, Kei Funston, Alison M. Bellare, Jayesh R. |
author_sort | Pal, Ruchi |
collection | PubMed |
description | [Image: see text] Electron energy-loss spectroscopy (EELS) is becoming an important tool in the characterization of polymeric materials. The sensitivity of EELS to changes in the chemical structure of polymeric materials dictates its applicability. In particular, it is important for compositional analysis to have reference spectra of pure components. Here, we report the spectra of the carbon K-edge of six polymers (polyethylene, polypropylene, polybutylene terephthalate, and polylactic acid) including copolymers (styrene acrylonitrile and acrylonitrile butadiene styrene), to be used as reference spectra for future EELS studies of polymers. We have successfully decomposed the carbon K-edge of each of the polymers and assigned the observed peaks to bonding transitions. The spectra have been acquired in standard experimental conditions, and electron beam damage has been taken into account during establishment of spectral–structural relationships. We found that the more commonly available low-energy resolution spectrometers are adequate to chemically fingerprint linear saturated hydrocarbons such as PE, PP, and PLA. We have thus moved a step closer toward creating an atlas of polymer EELS spectra, which can be subsequently used for chemical bond mapping of polymeric materials with nanoscale spatial resolution. |
format | Online Article Text |
id | pubmed-8459415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-84594152021-09-24 Chemical Fingerprinting of Polymers Using Electron Energy-Loss Spectroscopy Pal, Ruchi Bourgeois, Laure Weyland, Matthew Sikder, Arun K. Saito, Kei Funston, Alison M. Bellare, Jayesh R. ACS Omega [Image: see text] Electron energy-loss spectroscopy (EELS) is becoming an important tool in the characterization of polymeric materials. The sensitivity of EELS to changes in the chemical structure of polymeric materials dictates its applicability. In particular, it is important for compositional analysis to have reference spectra of pure components. Here, we report the spectra of the carbon K-edge of six polymers (polyethylene, polypropylene, polybutylene terephthalate, and polylactic acid) including copolymers (styrene acrylonitrile and acrylonitrile butadiene styrene), to be used as reference spectra for future EELS studies of polymers. We have successfully decomposed the carbon K-edge of each of the polymers and assigned the observed peaks to bonding transitions. The spectra have been acquired in standard experimental conditions, and electron beam damage has been taken into account during establishment of spectral–structural relationships. We found that the more commonly available low-energy resolution spectrometers are adequate to chemically fingerprint linear saturated hydrocarbons such as PE, PP, and PLA. We have thus moved a step closer toward creating an atlas of polymer EELS spectra, which can be subsequently used for chemical bond mapping of polymeric materials with nanoscale spatial resolution. American Chemical Society 2021-09-13 /pmc/articles/PMC8459415/ /pubmed/34568672 http://dx.doi.org/10.1021/acsomega.1c02939 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Pal, Ruchi Bourgeois, Laure Weyland, Matthew Sikder, Arun K. Saito, Kei Funston, Alison M. Bellare, Jayesh R. Chemical Fingerprinting of Polymers Using Electron Energy-Loss Spectroscopy |
title | Chemical Fingerprinting of Polymers Using Electron
Energy-Loss Spectroscopy |
title_full | Chemical Fingerprinting of Polymers Using Electron
Energy-Loss Spectroscopy |
title_fullStr | Chemical Fingerprinting of Polymers Using Electron
Energy-Loss Spectroscopy |
title_full_unstemmed | Chemical Fingerprinting of Polymers Using Electron
Energy-Loss Spectroscopy |
title_short | Chemical Fingerprinting of Polymers Using Electron
Energy-Loss Spectroscopy |
title_sort | chemical fingerprinting of polymers using electron
energy-loss spectroscopy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459415/ https://www.ncbi.nlm.nih.gov/pubmed/34568672 http://dx.doi.org/10.1021/acsomega.1c02939 |
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