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 in | Polymers Vol. 11; no. 5; p. 817 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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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.) |
Author_xml | – sequence: 1 givenname: Shin Won surname: Kim fullname: Kim, Shin Won email: 0shinmy0@yonsei.ac.kr organization: School of Mechanical Engineering, Yonsei University, 50, Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea. 0shinmy0@yonsei.ac.kr – sequence: 2 givenname: Joo Seong orcidid: 0000-0002-5499-0543 surname: Sohn fullname: Sohn, Joo Seong email: ssamjjang87@yonsei.ac.kr organization: School of Mechanical Engineering, Yonsei University, 50, Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea. ssamjjang87@yonsei.ac.kr – sequence: 3 givenname: Hyun Keun surname: Kim fullname: Kim, Hyun Keun email: sagegny@yonsei.ac.kr organization: School of Mechanical Engineering, Yonsei University, 50, Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea. sagegny@yonsei.ac.kr – sequence: 4 givenname: Youngjae orcidid: 0000-0003-3942-2254 surname: Ryu fullname: Ryu, Youngjae email: yjryu1027@yonsei.ac.kr organization: School of Mechanical Engineering, Yonsei University, 50, Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea. yjryu1027@yonsei.ac.kr – sequence: 5 givenname: Sung Woon surname: Cha fullname: Cha, Sung Woon email: swcha@yonsei.ac.kr organization: School of Mechanical Engineering, Yonsei University, 50, Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea. swcha@yonsei.ac.kr |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31067699$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_ijggc_2019_102930 crossref_primary_10_3390_polym12051173 crossref_primary_10_3390_polym15051153 crossref_primary_10_1364_OL_418096 crossref_primary_10_3390_polym12061313 crossref_primary_10_3390_polym14030596 crossref_primary_10_3390_polym16091276 crossref_primary_10_3390_polym13020232 crossref_primary_10_3390_nano11010094 |
Cites_doi | 10.1021/acs.macromol.6b00215 10.1021/ie404270g 10.1016/j.polymer.2013.10.037 10.1002/pen.760170304 10.1016/S0032-3861(03)00112-5 10.1115/1.2904310 10.1016/j.polymer.2016.05.018 10.1002/pen.20366 10.1021/ie8019483 |
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 |
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Keywords | gas adsorption impact strength polymer carbon dioxide tensile strength network density amorphous region polymer-gas mixture |
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References_xml | – ident: ref1 – ident: ref2 – volume: 49 start-page: 3987 year: 2016 ident: ref18 article-title: White Polymer Free Volume and Its Connection to the Glass Transition publication-title: Macromolecules doi: 10.1021/acs.macromol.6b00215 contributor: fullname: Ronald – volume: 2011 start-page: 9 year: 2011 ident: ref5 article-title: Fraunhofer UMSICHT studies customization of plastics via CO2 impregnation publication-title: Addit. Polym. – year: 2005 ident: ref6 contributor: fullname: Kim – year: 2016 ident: ref14 – ident: ref19 doi: 10.1021/ie404270g – volume: 54 start-page: 6860 year: 2013 ident: ref9 article-title: Stress induced lamellar thickening in poly(ethylene succinate) publication-title: Polymer doi: 10.1016/j.polymer.2013.10.037 contributor: fullname: Guoming – ident: ref8 doi: 10.1002/pen.760170304 – ident: ref17 doi: 10.1016/S0032-3861(03)00112-5 – volume: 24 start-page: 824 year: 2000 ident: ref3 article-title: Change of Glass Transition Temperature of PETG Containing Gas publication-title: Korean Soc. Mech. Eng. contributor: fullname: Cha – year: 2016 ident: ref15 – volume: 34 start-page: 579 year: 2010 ident: ref10 article-title: Investigation of Properties of the PET Film Dependent on the Biaxial Stretching publication-title: Polymer contributor: fullname: Lee – volume: 116 start-page: 439 year: 1994 ident: ref7 article-title: Experimental Characterization of the Tensile Behavior of Microcellular Polycarbonate Foams publication-title: J. Eng. Mater. Technol. doi: 10.1115/1.2904310 contributor: fullname: Vipin – ident: ref12 doi: 10.1016/j.polymer.2016.05.018 – volume: 45 start-page: 1639 year: 2005 ident: ref4 article-title: Effect of CO2 Sorption and Desorption on the Creep Response of Polycarbonate publication-title: Polym. Eng. Sci. doi: 10.1002/pen.20366 contributor: fullname: Arun – ident: ref11 – volume: 456 start-page: 174 year: 2015 ident: ref13 article-title: Study of volume swelling and interfacial tension of the polystyrene–carbon dioxide–dimethyl ether system publication-title: Polymer contributor: fullname: Mashmood – volume: 48 start-page: 7117 year: 2009 ident: ref16 article-title: Solubility and Diffusivity of Carbon Dioxide in Solid-State Isotactic Polypropylene by the Pressure-Decay Method publication-title: Ind. Eng. Chem. Res. doi: 10.1021/ie8019483 contributor: fullname: Da |
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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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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 |
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