Hydrolysis of aromatic polyurethane in water under high pressure of CO2

We have demonstrated a hydrolysis reaction of polyurethane (PU) under high pressure of carbon dioxide (CO2) in water. We employed the PU sample, poly(methylene bis-(1,4-phenylene)hexamethylene dicarbamate), denoted as M-PU, which was synthesized from 4,4′-diphenyl methane diisocyanate and 1,4-butane...

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Main Authors: Motokucho, Suguru, Yamaguchi, Akito, Nakayama, Yu, Morikawa, Hiroshi, Nakatani, Hisayuki
Format: Other/Unknown Material
Language:English
Published: Wiley Periodicals, Inc. 2017
Subjects:
Online Access:https://nagasaki-u.repo.nii.ac.jp/record/969/files/JPSpartA55_2004.pdf
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spelling ftnagasakiuniv:oai:nagasaki-u.repo.nii.ac.jp:00000969 2024-09-15T18:01:39+00:00 Hydrolysis of aromatic polyurethane in water under high pressure of CO2 Motokucho, Suguru Yamaguchi, Akito Nakayama, Yu Morikawa, Hiroshi Nakatani, Hisayuki 2017-03-16 application/pdf https://nagasaki-u.repo.nii.ac.jp/record/969/files/JPSpartA55_2004.pdf eng eng Wiley Periodicals, Inc. 10.1002/pola.28576 Journal of Polymer Science Part A: Polymer Chemistry 12 55 2004 2010 0887624X https://nagasaki-u.repo.nii.ac.jp/record/969/files/JPSpartA55_2004.pdf c 2017 Wiley Periodicals, Inc. This is the peer reviewed version of the following article: Journal of Polymer Science Part A: Polymer Chemistry, 55(12), pp.2004-2010; 2017, which has been published in final form at https://doi.org/10.1002/pola.28576. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. carbon dioxide carbonic acid degradation polyurethanes recycling AM 2017 ftnagasakiuniv 2024-08-23T06:19:41Z We have demonstrated a hydrolysis reaction of polyurethane (PU) under high pressure of carbon dioxide (CO2) in water. We employed the PU sample, poly(methylene bis-(1,4-phenylene)hexamethylene dicarbamate), denoted as M-PU, which was synthesized from 4,4′-diphenyl methane diisocyanate and 1,4-butane diol (BD). The optimum hydrolysis reaction condition was 190 °C under CO2 pressures over 4.1 MPa in water medium, and 93% hydrolysis of M-PU was achieved. After the reaction, the water-soluble parts were obtained, and isolated by column chromatography. The isolated products were 4,4′-methylenedianiline (MDA) and 1,4-butane diol (BD), which were components of repeating unit of M-PU. In addition, the hydrolysis reaction gave no byproduct. This hydrolysis under high pressure of CO2 with water is a reaction by which M-PU is selectively hydrolyzed into MDA and BD by cleaving urethane linkage. Moreover, the resulting hydrolyzed products were easily obtained by evaporation of aqueous layer after the reaction, indicating an efficient chemical recycling of PU was achieved. Journal of Polymer Science Part A: Polymer Chemistry, 55(12), pp.2004-2010; 2017 journal article Other/Unknown Material Carbonic acid NAOSITE: Nagasaki University Academic Output SITE
institution Open Polar
collection NAOSITE: Nagasaki University Academic Output SITE
op_collection_id ftnagasakiuniv
language English
topic carbon dioxide
carbonic acid
degradation
polyurethanes
recycling
spellingShingle carbon dioxide
carbonic acid
degradation
polyurethanes
recycling
Motokucho, Suguru
Yamaguchi, Akito
Nakayama, Yu
Morikawa, Hiroshi
Nakatani, Hisayuki
Hydrolysis of aromatic polyurethane in water under high pressure of CO2
topic_facet carbon dioxide
carbonic acid
degradation
polyurethanes
recycling
description We have demonstrated a hydrolysis reaction of polyurethane (PU) under high pressure of carbon dioxide (CO2) in water. We employed the PU sample, poly(methylene bis-(1,4-phenylene)hexamethylene dicarbamate), denoted as M-PU, which was synthesized from 4,4′-diphenyl methane diisocyanate and 1,4-butane diol (BD). The optimum hydrolysis reaction condition was 190 °C under CO2 pressures over 4.1 MPa in water medium, and 93% hydrolysis of M-PU was achieved. After the reaction, the water-soluble parts were obtained, and isolated by column chromatography. The isolated products were 4,4′-methylenedianiline (MDA) and 1,4-butane diol (BD), which were components of repeating unit of M-PU. In addition, the hydrolysis reaction gave no byproduct. This hydrolysis under high pressure of CO2 with water is a reaction by which M-PU is selectively hydrolyzed into MDA and BD by cleaving urethane linkage. Moreover, the resulting hydrolyzed products were easily obtained by evaporation of aqueous layer after the reaction, indicating an efficient chemical recycling of PU was achieved. Journal of Polymer Science Part A: Polymer Chemistry, 55(12), pp.2004-2010; 2017 journal article
format Other/Unknown Material
author Motokucho, Suguru
Yamaguchi, Akito
Nakayama, Yu
Morikawa, Hiroshi
Nakatani, Hisayuki
author_facet Motokucho, Suguru
Yamaguchi, Akito
Nakayama, Yu
Morikawa, Hiroshi
Nakatani, Hisayuki
author_sort Motokucho, Suguru
title Hydrolysis of aromatic polyurethane in water under high pressure of CO2
title_short Hydrolysis of aromatic polyurethane in water under high pressure of CO2
title_full Hydrolysis of aromatic polyurethane in water under high pressure of CO2
title_fullStr Hydrolysis of aromatic polyurethane in water under high pressure of CO2
title_full_unstemmed Hydrolysis of aromatic polyurethane in water under high pressure of CO2
title_sort hydrolysis of aromatic polyurethane in water under high pressure of co2
publisher Wiley Periodicals, Inc.
publishDate 2017
url https://nagasaki-u.repo.nii.ac.jp/record/969/files/JPSpartA55_2004.pdf
genre Carbonic acid
genre_facet Carbonic acid
op_relation 10.1002/pola.28576
Journal of Polymer Science Part A: Polymer Chemistry
12
55
2004
2010
0887624X
https://nagasaki-u.repo.nii.ac.jp/record/969/files/JPSpartA55_2004.pdf
op_rights c 2017 Wiley Periodicals, Inc. This is the peer reviewed version of the following article: Journal of Polymer Science Part A: Polymer Chemistry, 55(12), pp.2004-2010; 2017, which has been published in final form at https://doi.org/10.1002/pola.28576. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.
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