Poly(styrene/pentafluorostyrene)‐block‐poly(vinyl alcohol/vinylpyrrolidone) amphiphilic block copolymers for kinetic gas hydrate inhibitors: Synthesis, micellization behavior, and methane hydrate kinetic inhibition

ABSTRACT Amphiphilic block copolymers of short poly(styrene) (PS) or poly(2,3,4,5,6‐pentafluorostyrene) (PPFS) segments with comparatively longer poly(vinyl acetate) or poly(vinylpyrrolidone) (PVP) segments are synthesized using a 2‐cyanopropan‐2‐yl N ‐methyl‐ N ‐(pyridin‐4‐yl)dithiocarbamate switch...

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Published in:Journal of Polymer Science Part A: Polymer Chemistry
Main Authors: Rajput, Faraz, Colantuoni, Antonio, Bayahya, Salim, Dhane, Riadh, Servio, Phillip, Maric, Milan
Other Authors: McGill University, Natural Sciences and Engineering Research Council of Canada
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2018
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Online Access:http://dx.doi.org/10.1002/pola.29219
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spelling crwiley:10.1002/pola.29219 2024-06-23T07:54:37+00:00 Poly(styrene/pentafluorostyrene)‐block‐poly(vinyl alcohol/vinylpyrrolidone) amphiphilic block copolymers for kinetic gas hydrate inhibitors: Synthesis, micellization behavior, and methane hydrate kinetic inhibition Rajput, Faraz Colantuoni, Antonio Bayahya, Salim Dhane, Riadh Servio, Phillip Maric, Milan McGill University Natural Sciences and Engineering Research Council of Canada 2018 http://dx.doi.org/10.1002/pola.29219 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fpola.29219 https://onlinelibrary.wiley.com/doi/pdf/10.1002/pola.29219 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor Journal of Polymer Science Part A: Polymer Chemistry volume 56, issue 21, page 2445-2457 ISSN 0887-624X 1099-0518 journal-article 2018 crwiley https://doi.org/10.1002/pola.29219 2024-06-13T04:24:44Z ABSTRACT Amphiphilic block copolymers of short poly(styrene) (PS) or poly(2,3,4,5,6‐pentafluorostyrene) (PPFS) segments with comparatively longer poly(vinyl acetate) or poly(vinylpyrrolidone) (PVP) segments are synthesized using a 2‐cyanopropan‐2‐yl N ‐methyl‐ N ‐(pyridin‐4‐yl)dithiocarbamate switchable reversible addition–fragmentation chain transfer (RAFT) agent toward application as kinetic gas hydrate inhibitors (KHIs). Polymerization conditions are optimized to provide water‐soluble block copolymers by first polymerizing more activated monomers such as S and PFS to form a defined macro chain‐transfer agent (linear degree of polymerization with conversion, comparatively low dispersity) followed by chain extensions with less activated monomers VAc or VP by switching to the deprotonated form of the RAFT agent. The critical micelle concentrations of these amphiphilic block copolymers (after VAc unit hydrolysis to vinyl alcohol units) are measured using zeta surface potential measurements to estimate physical behavior once mixed with the hydrates. A PS‐poly(vinyl alcohol) block copolymer improved inhibition to 49% compared to the pure methane–water system with no KHIs. This inhibition was further reduced by 27% by substituting the PS with a more hydrophobic PPFS. A block copolymer of PS–PVP exhibited 20% greater inhibition than the PVP homopolymer and substituting PS with a more hydrophobic PPFS resulted in a 35% further decreased in methane KHI. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018 , 56 , 2445–2457, 56 , 2445–2457 Article in Journal/Newspaper Methane hydrate Wiley Online Library Journal of Polymer Science Part A: Polymer Chemistry 56 21 2445 2457
institution Open Polar
collection Wiley Online Library
op_collection_id crwiley
language English
description ABSTRACT Amphiphilic block copolymers of short poly(styrene) (PS) or poly(2,3,4,5,6‐pentafluorostyrene) (PPFS) segments with comparatively longer poly(vinyl acetate) or poly(vinylpyrrolidone) (PVP) segments are synthesized using a 2‐cyanopropan‐2‐yl N ‐methyl‐ N ‐(pyridin‐4‐yl)dithiocarbamate switchable reversible addition–fragmentation chain transfer (RAFT) agent toward application as kinetic gas hydrate inhibitors (KHIs). Polymerization conditions are optimized to provide water‐soluble block copolymers by first polymerizing more activated monomers such as S and PFS to form a defined macro chain‐transfer agent (linear degree of polymerization with conversion, comparatively low dispersity) followed by chain extensions with less activated monomers VAc or VP by switching to the deprotonated form of the RAFT agent. The critical micelle concentrations of these amphiphilic block copolymers (after VAc unit hydrolysis to vinyl alcohol units) are measured using zeta surface potential measurements to estimate physical behavior once mixed with the hydrates. A PS‐poly(vinyl alcohol) block copolymer improved inhibition to 49% compared to the pure methane–water system with no KHIs. This inhibition was further reduced by 27% by substituting the PS with a more hydrophobic PPFS. A block copolymer of PS–PVP exhibited 20% greater inhibition than the PVP homopolymer and substituting PS with a more hydrophobic PPFS resulted in a 35% further decreased in methane KHI. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018 , 56 , 2445–2457, 56 , 2445–2457
author2 McGill University
Natural Sciences and Engineering Research Council of Canada
format Article in Journal/Newspaper
author Rajput, Faraz
Colantuoni, Antonio
Bayahya, Salim
Dhane, Riadh
Servio, Phillip
Maric, Milan
spellingShingle Rajput, Faraz
Colantuoni, Antonio
Bayahya, Salim
Dhane, Riadh
Servio, Phillip
Maric, Milan
Poly(styrene/pentafluorostyrene)‐block‐poly(vinyl alcohol/vinylpyrrolidone) amphiphilic block copolymers for kinetic gas hydrate inhibitors: Synthesis, micellization behavior, and methane hydrate kinetic inhibition
author_facet Rajput, Faraz
Colantuoni, Antonio
Bayahya, Salim
Dhane, Riadh
Servio, Phillip
Maric, Milan
author_sort Rajput, Faraz
title Poly(styrene/pentafluorostyrene)‐block‐poly(vinyl alcohol/vinylpyrrolidone) amphiphilic block copolymers for kinetic gas hydrate inhibitors: Synthesis, micellization behavior, and methane hydrate kinetic inhibition
title_short Poly(styrene/pentafluorostyrene)‐block‐poly(vinyl alcohol/vinylpyrrolidone) amphiphilic block copolymers for kinetic gas hydrate inhibitors: Synthesis, micellization behavior, and methane hydrate kinetic inhibition
title_full Poly(styrene/pentafluorostyrene)‐block‐poly(vinyl alcohol/vinylpyrrolidone) amphiphilic block copolymers for kinetic gas hydrate inhibitors: Synthesis, micellization behavior, and methane hydrate kinetic inhibition
title_fullStr Poly(styrene/pentafluorostyrene)‐block‐poly(vinyl alcohol/vinylpyrrolidone) amphiphilic block copolymers for kinetic gas hydrate inhibitors: Synthesis, micellization behavior, and methane hydrate kinetic inhibition
title_full_unstemmed Poly(styrene/pentafluorostyrene)‐block‐poly(vinyl alcohol/vinylpyrrolidone) amphiphilic block copolymers for kinetic gas hydrate inhibitors: Synthesis, micellization behavior, and methane hydrate kinetic inhibition
title_sort poly(styrene/pentafluorostyrene)‐block‐poly(vinyl alcohol/vinylpyrrolidone) amphiphilic block copolymers for kinetic gas hydrate inhibitors: synthesis, micellization behavior, and methane hydrate kinetic inhibition
publisher Wiley
publishDate 2018
url http://dx.doi.org/10.1002/pola.29219
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fpola.29219
https://onlinelibrary.wiley.com/doi/pdf/10.1002/pola.29219
genre Methane hydrate
genre_facet Methane hydrate
op_source Journal of Polymer Science Part A: Polymer Chemistry
volume 56, issue 21, page 2445-2457
ISSN 0887-624X 1099-0518
op_rights http://onlinelibrary.wiley.com/termsAndConditions#vor
op_doi https://doi.org/10.1002/pola.29219
container_title Journal of Polymer Science Part A: Polymer Chemistry
container_volume 56
container_issue 21
container_start_page 2445
op_container_end_page 2457
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