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Improved Gas Hydrate Kinetic Inhibition for 5-Methyl-3-vinyl-2-oxazolidinone Copolymers and Synergists
[Image: see text] Kinetic hydrate inhibitors (KHIs) are used to prevent deposits and plugging of oil and gas production flow lines by gas hydrates. The key ingredient in a KHI formulation is a water-soluble amphiphilic polymer. Recently, polymers of a new commercially available 5-ring vinylic monome...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10413837/ https://www.ncbi.nlm.nih.gov/pubmed/37576614 http://dx.doi.org/10.1021/acsomega.3c03986 |
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author | Kelland, Malcolm A. Dirdal, Erik G. Ghosh, Radhakanta Ajiro, Hiroharu |
author_facet | Kelland, Malcolm A. Dirdal, Erik G. Ghosh, Radhakanta Ajiro, Hiroharu |
author_sort | Kelland, Malcolm A. |
collection | PubMed |
description | [Image: see text] Kinetic hydrate inhibitors (KHIs) are used to prevent deposits and plugging of oil and gas production flow lines by gas hydrates. The key ingredient in a KHI formulation is a water-soluble amphiphilic polymer. Recently, polymers of a new commercially available 5-ring vinylic monomer 5-methyl-3-vinyl-2-oxazolidinone (VMOX) were investigated as KHIs and shown to perform better than some commercial KHI polymers such as poly(N-vinyl pyrrolidone). This initial study using slow constant cooling (SCC) in rocking cells with a synthetic natural gas has now been expanded to further explore low molecular weight PVMOX homopolymers and VMOX copolymers as well as blends with nonpolymeric synergists. A PVMOX homopolymer with improved KHI performance was found using 3-mercaptoacetic acid as a chain transfer agent in the radical polymerization of VMOX. Among a range of copolymers, VMOX:n-butyl acrylate copolymers in particular gave good KHI performance, better than the PVMOX homopolymer. Among the potential synergists, trialkylamine oxides (alkyl = n-butyl or iso-pentyl) and tetra(n-pentyl)ammonium bromide to 2500 ppm were found to be antagonistic with PVMOX at the test concentrations while some alcohols and glycols were synergetic. The best synergist was 2,4,7,9-tetramethyl-5-decyne-4,7-diol (TMDD). For example, a mixture of 2500 ppm TMDD with 2500 ppm PVMOX (M(w) 2400 g/mol) performed significantly better than 5000 ppm PVMOX. Addition of 1250 ppm TMDD to 2500 ppm VMOX:n-butyl acrylate 6:4 copolymer lowered the hydrate onset temperature in SCC tests by a further 3 °C compared to the copolymer alone giving hydrate onset at 4.2 °C. |
format | Online Article Text |
id | pubmed-10413837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-104138372023-08-11 Improved Gas Hydrate Kinetic Inhibition for 5-Methyl-3-vinyl-2-oxazolidinone Copolymers and Synergists Kelland, Malcolm A. Dirdal, Erik G. Ghosh, Radhakanta Ajiro, Hiroharu ACS Omega [Image: see text] Kinetic hydrate inhibitors (KHIs) are used to prevent deposits and plugging of oil and gas production flow lines by gas hydrates. The key ingredient in a KHI formulation is a water-soluble amphiphilic polymer. Recently, polymers of a new commercially available 5-ring vinylic monomer 5-methyl-3-vinyl-2-oxazolidinone (VMOX) were investigated as KHIs and shown to perform better than some commercial KHI polymers such as poly(N-vinyl pyrrolidone). This initial study using slow constant cooling (SCC) in rocking cells with a synthetic natural gas has now been expanded to further explore low molecular weight PVMOX homopolymers and VMOX copolymers as well as blends with nonpolymeric synergists. A PVMOX homopolymer with improved KHI performance was found using 3-mercaptoacetic acid as a chain transfer agent in the radical polymerization of VMOX. Among a range of copolymers, VMOX:n-butyl acrylate copolymers in particular gave good KHI performance, better than the PVMOX homopolymer. Among the potential synergists, trialkylamine oxides (alkyl = n-butyl or iso-pentyl) and tetra(n-pentyl)ammonium bromide to 2500 ppm were found to be antagonistic with PVMOX at the test concentrations while some alcohols and glycols were synergetic. The best synergist was 2,4,7,9-tetramethyl-5-decyne-4,7-diol (TMDD). For example, a mixture of 2500 ppm TMDD with 2500 ppm PVMOX (M(w) 2400 g/mol) performed significantly better than 5000 ppm PVMOX. Addition of 1250 ppm TMDD to 2500 ppm VMOX:n-butyl acrylate 6:4 copolymer lowered the hydrate onset temperature in SCC tests by a further 3 °C compared to the copolymer alone giving hydrate onset at 4.2 °C. American Chemical Society 2023-07-25 /pmc/articles/PMC10413837/ /pubmed/37576614 http://dx.doi.org/10.1021/acsomega.3c03986 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Kelland, Malcolm A. Dirdal, Erik G. Ghosh, Radhakanta Ajiro, Hiroharu Improved Gas Hydrate Kinetic Inhibition for 5-Methyl-3-vinyl-2-oxazolidinone Copolymers and Synergists |
title | Improved Gas Hydrate Kinetic Inhibition for 5-Methyl-3-vinyl-2-oxazolidinone
Copolymers and Synergists |
title_full | Improved Gas Hydrate Kinetic Inhibition for 5-Methyl-3-vinyl-2-oxazolidinone
Copolymers and Synergists |
title_fullStr | Improved Gas Hydrate Kinetic Inhibition for 5-Methyl-3-vinyl-2-oxazolidinone
Copolymers and Synergists |
title_full_unstemmed | Improved Gas Hydrate Kinetic Inhibition for 5-Methyl-3-vinyl-2-oxazolidinone
Copolymers and Synergists |
title_short | Improved Gas Hydrate Kinetic Inhibition for 5-Methyl-3-vinyl-2-oxazolidinone
Copolymers and Synergists |
title_sort | improved gas hydrate kinetic inhibition for 5-methyl-3-vinyl-2-oxazolidinone
copolymers and synergists |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10413837/ https://www.ncbi.nlm.nih.gov/pubmed/37576614 http://dx.doi.org/10.1021/acsomega.3c03986 |
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