Cargando…

FTIR product study of the Cl-initiated oxidation products of CFC replacements: (E/Z)-1,2,3,3,3-pentafluoropropene and hexafluoroisobutylene

A product study of the reactions of (E/Z)-1,2,3,3,3-pentafluoropropene ((E/Z)-CF(3)CF[double bond, length as m-dash]CHF) and hexafluoroisobutylene ((CF(3))(2)C[double bond, length as m-dash]CH(2)) initiated by Cl atoms were developed at 298 ± 2 K and atmospheric pressure. The experiments were carrie...

Descripción completa

Detalles Bibliográficos
Autores principales: Rivela, Cynthia B., Gibilisco, Rodrigo G., Tovar, Carmen M., Barnes, Ian, Wiesen, Peter, Blanco, María B., Teruel, Mariano A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8696996/
https://www.ncbi.nlm.nih.gov/pubmed/35423798
http://dx.doi.org/10.1039/d1ra00283j
_version_ 1784619946035118080
author Rivela, Cynthia B.
Gibilisco, Rodrigo G.
Tovar, Carmen M.
Barnes, Ian
Wiesen, Peter
Blanco, María B.
Teruel, Mariano A.
author_facet Rivela, Cynthia B.
Gibilisco, Rodrigo G.
Tovar, Carmen M.
Barnes, Ian
Wiesen, Peter
Blanco, María B.
Teruel, Mariano A.
author_sort Rivela, Cynthia B.
collection PubMed
description A product study of the reactions of (E/Z)-1,2,3,3,3-pentafluoropropene ((E/Z)-CF(3)CF[double bond, length as m-dash]CHF) and hexafluoroisobutylene ((CF(3))(2)C[double bond, length as m-dash]CH(2)) initiated by Cl atoms were developed at 298 ± 2 K and atmospheric pressure. The experiments were carried out in a 1080 L quartz-glass environmental chamber coupled via in situ FTIR spectroscopy to monitor the reactants and products. The main products observed and their yields were as follows: CF(3)C(O)F (106 ± 9)% with HC(O)F (100 ± 8)% as a co-product for (E/Z)-CF(3)CF[double bond, length as m-dash]CHF, and CF(3)C(O)CF(3) (94 ± 5)% with HC(O)Cl (90 ± 7)% as a co-product for (CF(3))(2)C[double bond, length as m-dash]CH(2). Atmospheric implications of the end-product degradation are assessed in terms of their impact on ecosystems to help environmental policymakers consider HFOs as acceptable replacements.
format Online
Article
Text
id pubmed-8696996
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-86969962022-04-13 FTIR product study of the Cl-initiated oxidation products of CFC replacements: (E/Z)-1,2,3,3,3-pentafluoropropene and hexafluoroisobutylene Rivela, Cynthia B. Gibilisco, Rodrigo G. Tovar, Carmen M. Barnes, Ian Wiesen, Peter Blanco, María B. Teruel, Mariano A. RSC Adv Chemistry A product study of the reactions of (E/Z)-1,2,3,3,3-pentafluoropropene ((E/Z)-CF(3)CF[double bond, length as m-dash]CHF) and hexafluoroisobutylene ((CF(3))(2)C[double bond, length as m-dash]CH(2)) initiated by Cl atoms were developed at 298 ± 2 K and atmospheric pressure. The experiments were carried out in a 1080 L quartz-glass environmental chamber coupled via in situ FTIR spectroscopy to monitor the reactants and products. The main products observed and their yields were as follows: CF(3)C(O)F (106 ± 9)% with HC(O)F (100 ± 8)% as a co-product for (E/Z)-CF(3)CF[double bond, length as m-dash]CHF, and CF(3)C(O)CF(3) (94 ± 5)% with HC(O)Cl (90 ± 7)% as a co-product for (CF(3))(2)C[double bond, length as m-dash]CH(2). Atmospheric implications of the end-product degradation are assessed in terms of their impact on ecosystems to help environmental policymakers consider HFOs as acceptable replacements. The Royal Society of Chemistry 2021-04-01 /pmc/articles/PMC8696996/ /pubmed/35423798 http://dx.doi.org/10.1039/d1ra00283j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Rivela, Cynthia B.
Gibilisco, Rodrigo G.
Tovar, Carmen M.
Barnes, Ian
Wiesen, Peter
Blanco, María B.
Teruel, Mariano A.
FTIR product study of the Cl-initiated oxidation products of CFC replacements: (E/Z)-1,2,3,3,3-pentafluoropropene and hexafluoroisobutylene
title FTIR product study of the Cl-initiated oxidation products of CFC replacements: (E/Z)-1,2,3,3,3-pentafluoropropene and hexafluoroisobutylene
title_full FTIR product study of the Cl-initiated oxidation products of CFC replacements: (E/Z)-1,2,3,3,3-pentafluoropropene and hexafluoroisobutylene
title_fullStr FTIR product study of the Cl-initiated oxidation products of CFC replacements: (E/Z)-1,2,3,3,3-pentafluoropropene and hexafluoroisobutylene
title_full_unstemmed FTIR product study of the Cl-initiated oxidation products of CFC replacements: (E/Z)-1,2,3,3,3-pentafluoropropene and hexafluoroisobutylene
title_short FTIR product study of the Cl-initiated oxidation products of CFC replacements: (E/Z)-1,2,3,3,3-pentafluoropropene and hexafluoroisobutylene
title_sort ftir product study of the cl-initiated oxidation products of cfc replacements: (e/z)-1,2,3,3,3-pentafluoropropene and hexafluoroisobutylene
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8696996/
https://www.ncbi.nlm.nih.gov/pubmed/35423798
http://dx.doi.org/10.1039/d1ra00283j
work_keys_str_mv AT rivelacynthiab ftirproductstudyoftheclinitiatedoxidationproductsofcfcreplacementsez12333pentafluoropropeneandhexafluoroisobutylene
AT gibiliscorodrigog ftirproductstudyoftheclinitiatedoxidationproductsofcfcreplacementsez12333pentafluoropropeneandhexafluoroisobutylene
AT tovarcarmenm ftirproductstudyoftheclinitiatedoxidationproductsofcfcreplacementsez12333pentafluoropropeneandhexafluoroisobutylene
AT barnesian ftirproductstudyoftheclinitiatedoxidationproductsofcfcreplacementsez12333pentafluoropropeneandhexafluoroisobutylene
AT wiesenpeter ftirproductstudyoftheclinitiatedoxidationproductsofcfcreplacementsez12333pentafluoropropeneandhexafluoroisobutylene
AT blancomariab ftirproductstudyoftheclinitiatedoxidationproductsofcfcreplacementsez12333pentafluoropropeneandhexafluoroisobutylene
AT teruelmarianoa ftirproductstudyoftheclinitiatedoxidationproductsofcfcreplacementsez12333pentafluoropropeneandhexafluoroisobutylene