Environment-friendly chemical recycling of aliphatic polyurethanes by hydrolysis in a CO2-water system

In order to develop a chemical recycling system of polyurethanes (PUs), environment-friendly hydrolysis of two types of aliphatic PUs was studied under pressured CO2 in water, in which the carbonic acid generated from CO2 acted as an acid catalyst. Two PUs, namely H-PU or I-PU, were synthesized star...

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Main Authors: Motokucho, Suguru, 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/970/files/JAPS135_45897.pdf
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spelling ftnagasakiuniv:oai:nagasaki-u.repo.nii.ac.jp:00000970 2024-09-15T18:01:40+00:00 Environment-friendly chemical recycling of aliphatic polyurethanes by hydrolysis in a CO2-water system Motokucho, Suguru Nakayama, Yu Morikawa, Hiroshi Nakatani, Hisayuki 2017-10-26 application/pdf https://nagasaki-u.repo.nii.ac.jp/record/970/files/JAPS135_45897.pdf eng eng Wiley Periodicals, Inc. 10.1002/app.45897 Journal of Applied Polymer Science, 135(8), art.no.45897; 2017 8 135 45897 00218995 https://nagasaki-u.repo.nii.ac.jp/record/970/files/JAPS135_45897.pdf c 2017 Wiley Periodicals, Inc. This is the peer reviewed version of the following article: Journal of Applied Polymer Science, 135(8), art.no.45897; 2017, which has been published in final form at https://doi.org/10.1002/app.45897. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. degradation polyurethane recycling AM 2017 ftnagasakiuniv 2024-08-23T06:19:41Z In order to develop a chemical recycling system of polyurethanes (PUs), environment-friendly hydrolysis of two types of aliphatic PUs was studied under pressured CO2 in water, in which the carbonic acid generated from CO2 acted as an acid catalyst. Two PUs, namely H-PU or I-PU, were synthesized starting from 1,4-butanediol and 1,6-hexamethylene diisocyanate or isophorone diisocyanate, respectively. The hydrolysis of PUs depended on the experimental conditions, such as the temperature and CO2 pressure. As a result, 98% of H-PU and 91% of I-PU were successfully hydrolyzed under the typical conditions of 190?°C for 24 h at 8.0 MPa CO2. The reaction mixtures afforded 1,4-butanediol and diamines without the formation of any byproducts. Both of these raw materials generated from the originated PUs by selective hydrolytic cleavage of the urethane linkages, and they were easily isolated in high yields simply by evaporation of the water-soluble components within the reaction mixture. By comparing the results of the two aliphatic PUs with those of an aromatic PU (M-PU), the hydrolyzability was found to decrease in the order H-PU, I-PU, and M-PU. The difference can be ascribed to the hydrophilicity of the aliphatic or aromatic groups connected to the urethane moieties at the terminals of PUs. Journal of Applied Polymer Science 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 degradation
polyurethane
recycling
spellingShingle degradation
polyurethane
recycling
Motokucho, Suguru
Nakayama, Yu
Morikawa, Hiroshi
Nakatani, Hisayuki
Environment-friendly chemical recycling of aliphatic polyurethanes by hydrolysis in a CO2-water system
topic_facet degradation
polyurethane
recycling
description In order to develop a chemical recycling system of polyurethanes (PUs), environment-friendly hydrolysis of two types of aliphatic PUs was studied under pressured CO2 in water, in which the carbonic acid generated from CO2 acted as an acid catalyst. Two PUs, namely H-PU or I-PU, were synthesized starting from 1,4-butanediol and 1,6-hexamethylene diisocyanate or isophorone diisocyanate, respectively. The hydrolysis of PUs depended on the experimental conditions, such as the temperature and CO2 pressure. As a result, 98% of H-PU and 91% of I-PU were successfully hydrolyzed under the typical conditions of 190?°C for 24 h at 8.0 MPa CO2. The reaction mixtures afforded 1,4-butanediol and diamines without the formation of any byproducts. Both of these raw materials generated from the originated PUs by selective hydrolytic cleavage of the urethane linkages, and they were easily isolated in high yields simply by evaporation of the water-soluble components within the reaction mixture. By comparing the results of the two aliphatic PUs with those of an aromatic PU (M-PU), the hydrolyzability was found to decrease in the order H-PU, I-PU, and M-PU. The difference can be ascribed to the hydrophilicity of the aliphatic or aromatic groups connected to the urethane moieties at the terminals of PUs. Journal of Applied Polymer Science journal article
format Other/Unknown Material
author Motokucho, Suguru
Nakayama, Yu
Morikawa, Hiroshi
Nakatani, Hisayuki
author_facet Motokucho, Suguru
Nakayama, Yu
Morikawa, Hiroshi
Nakatani, Hisayuki
author_sort Motokucho, Suguru
title Environment-friendly chemical recycling of aliphatic polyurethanes by hydrolysis in a CO2-water system
title_short Environment-friendly chemical recycling of aliphatic polyurethanes by hydrolysis in a CO2-water system
title_full Environment-friendly chemical recycling of aliphatic polyurethanes by hydrolysis in a CO2-water system
title_fullStr Environment-friendly chemical recycling of aliphatic polyurethanes by hydrolysis in a CO2-water system
title_full_unstemmed Environment-friendly chemical recycling of aliphatic polyurethanes by hydrolysis in a CO2-water system
title_sort environment-friendly chemical recycling of aliphatic polyurethanes by hydrolysis in a co2-water system
publisher Wiley Periodicals, Inc.
publishDate 2017
url https://nagasaki-u.repo.nii.ac.jp/record/970/files/JAPS135_45897.pdf
genre Carbonic acid
genre_facet Carbonic acid
op_relation 10.1002/app.45897
Journal of Applied Polymer Science, 135(8), art.no.45897; 2017
8
135
45897
00218995
https://nagasaki-u.repo.nii.ac.jp/record/970/files/JAPS135_45897.pdf
op_rights c 2017 Wiley Periodicals, Inc. This is the peer reviewed version of the following article: Journal of Applied Polymer Science, 135(8), art.no.45897; 2017, which has been published in final form at https://doi.org/10.1002/app.45897. 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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