Effects of Gas Adsorption on the Mechanical Properties of Amorphous Polymer

This study investigates the properties of a polymer-gas mixture formed through diffusion, based on the changes in the partial pressure and observed changes in the impact and tensile strengths owing to the gas dissolution. The high-pressure gas dissolves into a solid-state polymer through diffusion b...

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Published inPolymers Vol. 11; no. 5; p. 817
Main Authors Kim, Shin Won, Sohn, Joo Seong, Kim, Hyun Keun, Ryu, Youngjae, Cha, Sung Woon
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 07.05.2019
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Abstract This study investigates the properties of a polymer-gas mixture formed through diffusion, based on the changes in the partial pressure and observed changes in the impact and tensile strengths owing to the gas dissolution. The high-pressure gas dissolves into a solid-state polymer through diffusion based on the difference in the partial pressure. This dissolved gas is present in the amorphous region within the polymeric material temporarily, which results in the polymer exhibiting different mechanical properties, while the gas remains dissolved in the polymer. In this study, the mechanical properties of amorphous polyethylene terephthalate (APET) specimens prepared by dissolving CO using a high-pressure vessel were investigated, and the resulting impact and tensile strengths were measured. These experiments showed that the increase in sorption rate of CO caused an increase in the impact strength. At 2.9% CO absorption, the impact strength of APET increased 956% compared to that of the reference specimen. Furthermore, the tensile strength decreased by up to 71.7% at 5.48% CO sorption; the stress-strain curves varied with the gas sorption rate. This phenomenon can be associated with the change in the volume caused by CO dissolution. When the APET absorbed more than 2.0% CO gas, sample volume increased. A decrease in the network density can occur when the volume is increased while maintaining constant mass. The CO gas in the polymer acted as a cushion in impact tests which have sorption rates above 2%. In addition to the reduction in the network density in the polymer chain, Van Der Waals forces are decreased causing a decrease in tensile strength only while CO is present in the APET. These observations only occur prior to CO desorption from the polymer.
AbstractList This study investigates the properties of a polymer–gas mixture formed through diffusion, based on the changes in the partial pressure and observed changes in the impact and tensile strengths owing to the gas dissolution. The high-pressure gas dissolves into a solid-state polymer through diffusion based on the difference in the partial pressure. This dissolved gas is present in the amorphous region within the polymeric material temporarily, which results in the polymer exhibiting different mechanical properties, while the gas remains dissolved in the polymer. In this study, the mechanical properties of amorphous polyethylene terephthalate (APET) specimens prepared by dissolving CO2 using a high-pressure vessel were investigated, and the resulting impact and tensile strengths were measured. These experiments showed that the increase in sorption rate of CO2 caused an increase in the impact strength. At 2.9% CO2 absorption, the impact strength of APET increased 956% compared to that of the reference specimen. Furthermore, the tensile strength decreased by up to 71.7% at 5.48% CO2 sorption; the stress–strain curves varied with the gas sorption rate. This phenomenon can be associated with the change in the volume caused by CO2 dissolution. When the APET absorbed more than 2.0% CO2 gas, sample volume increased. A decrease in the network density can occur when the volume is increased while maintaining constant mass. The CO2 gas in the polymer acted as a cushion in impact tests which have sorption rates above 2%. In addition to the reduction in the network density in the polymer chain, Van Der Waals forces are decreased causing a decrease in tensile strength only while CO2 is present in the APET. These observations only occur prior to CO2 desorption from the polymer.
This study investigates the properties of a polymer-gas mixture formed through diffusion, based on the changes in the partial pressure and observed changes in the impact and tensile strengths owing to the gas dissolution. The high-pressure gas dissolves into a solid-state polymer through diffusion based on the difference in the partial pressure. This dissolved gas is present in the amorphous region within the polymeric material temporarily, which results in the polymer exhibiting different mechanical properties, while the gas remains dissolved in the polymer. In this study, the mechanical properties of amorphous polyethylene terephthalate (APET) specimens prepared by dissolving CO using a high-pressure vessel were investigated, and the resulting impact and tensile strengths were measured. These experiments showed that the increase in sorption rate of CO caused an increase in the impact strength. At 2.9% CO absorption, the impact strength of APET increased 956% compared to that of the reference specimen. Furthermore, the tensile strength decreased by up to 71.7% at 5.48% CO sorption; the stress-strain curves varied with the gas sorption rate. This phenomenon can be associated with the change in the volume caused by CO dissolution. When the APET absorbed more than 2.0% CO gas, sample volume increased. A decrease in the network density can occur when the volume is increased while maintaining constant mass. The CO gas in the polymer acted as a cushion in impact tests which have sorption rates above 2%. In addition to the reduction in the network density in the polymer chain, Van Der Waals forces are decreased causing a decrease in tensile strength only while CO is present in the APET. These observations only occur prior to CO desorption from the polymer.
This study investigates the properties of a polymer–gas mixture formed through diffusion, based on the changes in the partial pressure and observed changes in the impact and tensile strengths owing to the gas dissolution. The high-pressure gas dissolves into a solid-state polymer through diffusion based on the difference in the partial pressure. This dissolved gas is present in the amorphous region within the polymeric material temporarily, which results in the polymer exhibiting different mechanical properties, while the gas remains dissolved in the polymer. In this study, the mechanical properties of amorphous polyethylene terephthalate (APET) specimens prepared by dissolving CO 2 using a high-pressure vessel were investigated, and the resulting impact and tensile strengths were measured. These experiments showed that the increase in sorption rate of CO 2 caused an increase in the impact strength. At 2.9% CO 2 absorption, the impact strength of APET increased 956% compared to that of the reference specimen. Furthermore, the tensile strength decreased by up to 71.7% at 5.48% CO 2 sorption; the stress–strain curves varied with the gas sorption rate. This phenomenon can be associated with the change in the volume caused by CO 2 dissolution. When the APET absorbed more than 2.0% CO 2 gas, sample volume increased. A decrease in the network density can occur when the volume is increased while maintaining constant mass. The CO 2 gas in the polymer acted as a cushion in impact tests which have sorption rates above 2%. In addition to the reduction in the network density in the polymer chain, Van Der Waals forces are decreased causing a decrease in tensile strength only while CO 2 is present in the APET. These observations only occur prior to CO 2 desorption from the polymer.
This study investigates the properties of a polymer−gas mixture formed through diffusion, based on the changes in the partial pressure and observed changes in the impact and tensile strengths owing to the gas dissolution. The high-pressure gas dissolves into a solid-state polymer through diffusion based on the difference in the partial pressure. This dissolved gas is present in the amorphous region within the polymeric material temporarily, which results in the polymer exhibiting different mechanical properties, while the gas remains dissolved in the polymer. In this study, the mechanical properties of amorphous polyethylene terephthalate (APET) specimens prepared by dissolving CO2 using a high-pressure vessel were investigated, and the resulting impact and tensile strengths were measured. These experiments showed that the increase in sorption rate of CO2 caused an increase in the impact strength. At 2.9% CO2 absorption, the impact strength of APET increased 956% compared to that of the reference specimen. Furthermore, the tensile strength decreased by up to 71.7% at 5.48% CO2 sorption; the stress−strain curves varied with the gas sorption rate. This phenomenon can be associated with the change in the volume caused by CO2 dissolution. When the APET absorbed more than 2.0% CO2 gas, sample volume increased. A decrease in the network density can occur when the volume is increased while maintaining constant mass. The CO2 gas in the polymer acted as a cushion in impact tests which have sorption rates above 2%. In addition to the reduction in the network density in the polymer chain, Van Der Waals forces are decreased causing a decrease in tensile strength only while CO2 is present in the APET. These observations only occur prior to CO2 desorption from the polymer.
Author Kim, Shin Won
Kim, Hyun Keun
Ryu, Youngjae
Cha, Sung Woon
Sohn, Joo Seong
AuthorAffiliation School of Mechanical Engineering, Yonsei University, 50, Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea; 0shinmy0@yonsei.ac.kr (S.W.K.); ssamjjang87@yonsei.ac.kr (J.S.S.); sagegny@yonsei.ac.kr (H.K.K.); yjryu1027@yonsei.ac.kr (Y.R.)
AuthorAffiliation_xml – name: School of Mechanical Engineering, Yonsei University, 50, Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea; 0shinmy0@yonsei.ac.kr (S.W.K.); ssamjjang87@yonsei.ac.kr (J.S.S.); sagegny@yonsei.ac.kr (H.K.K.); yjryu1027@yonsei.ac.kr (Y.R.)
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/31067699$$D View this record in MEDLINE/PubMed
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crossref_primary_10_1364_OL_418096
crossref_primary_10_3390_polym12061313
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10.1021/ie404270g
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ContentType Journal Article
Copyright 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
2019 by the authors. 2019
Copyright_xml – notice: 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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Issue 5
Keywords gas adsorption
impact strength
polymer
carbon dioxide
tensile strength
network density
amorphous region
polymer-gas mixture
Language English
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Snippet This study investigates the properties of a polymer-gas mixture formed through diffusion, based on the changes in the partial pressure and observed changes in...
This study investigates the properties of a polymer–gas mixture formed through diffusion, based on the changes in the partial pressure and observed changes in...
This study investigates the properties of a polymer−gas mixture formed through diffusion, based on the changes in the partial pressure and observed changes in...
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StartPage 817
SubjectTerms Adsorption
Amorphous materials
amorphous region
Carbon dioxide
Cushions
Density
Dissolution
Dissolved gases
Experiments
gas adsorption
Gas mixtures
Gases
Impact strength
Impact tests
Mechanical properties
network density
Partial pressure
Polyethylene terephthalate
polymer
polymer-gas mixture
Polymers
Pressure vessels
Sorption
Stress-strain curves
Tensile strength
Van der Waals forces
Viscosity
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Title Effects of Gas Adsorption on the Mechanical Properties of Amorphous Polymer
URI https://www.ncbi.nlm.nih.gov/pubmed/31067699
https://www.proquest.com/docview/2557236754
https://search.proquest.com/docview/2231941431
https://pubmed.ncbi.nlm.nih.gov/PMC6572250
https://doaj.org/article/3a72aa5f7d9e498d8478d5c66f2aa651
Volume 11
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