SURFACE REARRANGEMENTS OF OXYGEN PLASMA TREATED POLYSTYRENE: SURFACE DYNAMICS AND HUMIDITY EFFECT

The time evolution of oxygen plasma treated polystyrene (PS) surfaces was investigated upon storing them in the air under controlled humidity conditions. The methods of water contact angle, X-ray photoelectron spectroscopy (XPS), sum frequency generation (SFG) vibrational spectroscopy, and atomic fo...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Chinese journal of polymer science 2005-03, Vol.23 (2), p.187-196
Hauptverfasser: Li, Junwei, Oh, Kyunghui, Yu, Hyuk
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 196
container_issue 2
container_start_page 187
container_title Chinese journal of polymer science
container_volume 23
creator Li, Junwei
Oh, Kyunghui
Yu, Hyuk
description The time evolution of oxygen plasma treated polystyrene (PS) surfaces was investigated upon storing them in the air under controlled humidity conditions. The methods of water contact angle, X-ray photoelectron spectroscopy (XPS), sum frequency generation (SFG) vibrational spectroscopy, and atomic force microscopy (AFM) were used to infer the surface properties and structure. Chemical groups containing oxygen were formed on the PS surface with the plasma treatment,demonstrated by water contact angle and XPS. The surface polarity decayed markedly on time, as assessed by steady increasein the water contact angle as a function of storage time, from zero to around 60°. The observed decay is interpreted as arising from surface rearrangement processes to burying polar groups away from the uppermost layer of the surfaces, which is in contact with air. On the other hand, XPS results show that the chemical composition in the first 3 nm surface layer is unaffected by the surface aging, and the depth profile of oxygen is essentially the same with time. A possible change of PS surface roughness was examined by AFM, and it showed that the increase of water contact angle during surface aging could not be attributed to surface roughness. Thus, it is concluded that surface aging is attributable to surface reorganization and the motion of oxygen containing groups is confined within the XPS probing depth. SFG spectroscopy, which is intrinsically interface-specific, was used to detect the chemical structure of PS surface at the molecular level after various aging times.The results are interpreted as follows. During the aging of the plasma treated PS surfaces, the oxygen containing groups undergo reorientation processes toward the polymer bulk and/or parallel to the surface, while the CH2 moiety stands up on the PS surface. Our results indicate that the surface configuration changes do not require large length scale segmental motions or migration of macromolecules. Motions that are responsible for surface configuration changes could be relatively small rotational motions. The aging behaviors under different relative humidity conditions were shown to be similar from 18% to 91%, whereas the kinetics of surface polarity decays were faster in higher relative humidity. Here, the surface rearrangement of polystyrene films that were previously treated by oxygen plasma and aged, and was investigated in terms of contact angle after the water immersion. The contact angles of the water-i
doi_str_mv 10.1142/S0256767905000266
format Article
fullrecord <record><control><sourceid>proquest_chong</sourceid><recordid>TN_cdi_proquest_miscellaneous_29592247</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cqvip_id>15587558</cqvip_id><sourcerecordid>29592247</sourcerecordid><originalsourceid>FETCH-LOGICAL-c261t-d7dd013df032d580df671d94e970da7aebc86ec7a210d237ca7dbea5e687fc1f3</originalsourceid><addsrcrecordid>eNo1jEtOwzAARC0EEqVwAHYWC3YB24ntZGklThspnypJJbKKXNsphdDSpr0MZ-FOXIFWhcVoFu_NAHCP0RPGHnmuEKGMMx4gihAijF2AEfbcwGEEuZdgdMLOiV-Dm2F4Q4h5nPIR0NW8jEUoYSlFWYp8IjOZ1xUsYli8NBOZw1kqqkzA-ijUMoKzIm2quillLn--v-D_PGpykSVhBUUewek8S6KkbqCMYxnWt-CqU_1g7_56DOaxrMOpkxaTJBSpownDe8dwYxB2TYdcYqiPTMc4NoFnA46M4soutM-s5opgZIjLteJmYRW1zOedxp07Bo_n38_dZnuww779WA3a9r1a281haElAA0I8fhQfzqJ-3ayX29V62S6Ufu9WvW0xpT4_xv0FON1eVA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>29592247</pqid></control><display><type>article</type><title>SURFACE REARRANGEMENTS OF OXYGEN PLASMA TREATED POLYSTYRENE: SURFACE DYNAMICS AND HUMIDITY EFFECT</title><source>Alma/SFX Local Collection</source><creator>Li, Junwei ; Oh, Kyunghui ; Yu, Hyuk</creator><creatorcontrib>Li, Junwei ; Oh, Kyunghui ; Yu, Hyuk</creatorcontrib><description>The time evolution of oxygen plasma treated polystyrene (PS) surfaces was investigated upon storing them in the air under controlled humidity conditions. The methods of water contact angle, X-ray photoelectron spectroscopy (XPS), sum frequency generation (SFG) vibrational spectroscopy, and atomic force microscopy (AFM) were used to infer the surface properties and structure. Chemical groups containing oxygen were formed on the PS surface with the plasma treatment,demonstrated by water contact angle and XPS. The surface polarity decayed markedly on time, as assessed by steady increasein the water contact angle as a function of storage time, from zero to around 60°. The observed decay is interpreted as arising from surface rearrangement processes to burying polar groups away from the uppermost layer of the surfaces, which is in contact with air. On the other hand, XPS results show that the chemical composition in the first 3 nm surface layer is unaffected by the surface aging, and the depth profile of oxygen is essentially the same with time. A possible change of PS surface roughness was examined by AFM, and it showed that the increase of water contact angle during surface aging could not be attributed to surface roughness. Thus, it is concluded that surface aging is attributable to surface reorganization and the motion of oxygen containing groups is confined within the XPS probing depth. SFG spectroscopy, which is intrinsically interface-specific, was used to detect the chemical structure of PS surface at the molecular level after various aging times.The results are interpreted as follows. During the aging of the plasma treated PS surfaces, the oxygen containing groups undergo reorientation processes toward the polymer bulk and/or parallel to the surface, while the CH2 moiety stands up on the PS surface. Our results indicate that the surface configuration changes do not require large length scale segmental motions or migration of macromolecules. Motions that are responsible for surface configuration changes could be relatively small rotational motions. The aging behaviors under different relative humidity conditions were shown to be similar from 18% to 91%, whereas the kinetics of surface polarity decays were faster in higher relative humidity. Here, the surface rearrangement of polystyrene films that were previously treated by oxygen plasma and aged, and was investigated in terms of contact angle after the water immersion. The contact angles of the water-immersed samples were found to change and approach the initial values before the immersion asymptotically.</description><identifier>ISSN: 0256-7679</identifier><identifier>EISSN: 1439-6203</identifier><identifier>DOI: 10.1142/S0256767905000266</identifier><language>eng</language><subject>氧等离子体 ; 聚苯乙烯 ; 表面处理</subject><ispartof>Chinese journal of polymer science, 2005-03, Vol.23 (2), p.187-196</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c261t-d7dd013df032d580df671d94e970da7aebc86ec7a210d237ca7dbea5e687fc1f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/86788X/86788X.jpg</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Li, Junwei</creatorcontrib><creatorcontrib>Oh, Kyunghui</creatorcontrib><creatorcontrib>Yu, Hyuk</creatorcontrib><title>SURFACE REARRANGEMENTS OF OXYGEN PLASMA TREATED POLYSTYRENE: SURFACE DYNAMICS AND HUMIDITY EFFECT</title><title>Chinese journal of polymer science</title><addtitle>Chinese Journal of Polymer Science</addtitle><description>The time evolution of oxygen plasma treated polystyrene (PS) surfaces was investigated upon storing them in the air under controlled humidity conditions. The methods of water contact angle, X-ray photoelectron spectroscopy (XPS), sum frequency generation (SFG) vibrational spectroscopy, and atomic force microscopy (AFM) were used to infer the surface properties and structure. Chemical groups containing oxygen were formed on the PS surface with the plasma treatment,demonstrated by water contact angle and XPS. The surface polarity decayed markedly on time, as assessed by steady increasein the water contact angle as a function of storage time, from zero to around 60°. The observed decay is interpreted as arising from surface rearrangement processes to burying polar groups away from the uppermost layer of the surfaces, which is in contact with air. On the other hand, XPS results show that the chemical composition in the first 3 nm surface layer is unaffected by the surface aging, and the depth profile of oxygen is essentially the same with time. A possible change of PS surface roughness was examined by AFM, and it showed that the increase of water contact angle during surface aging could not be attributed to surface roughness. Thus, it is concluded that surface aging is attributable to surface reorganization and the motion of oxygen containing groups is confined within the XPS probing depth. SFG spectroscopy, which is intrinsically interface-specific, was used to detect the chemical structure of PS surface at the molecular level after various aging times.The results are interpreted as follows. During the aging of the plasma treated PS surfaces, the oxygen containing groups undergo reorientation processes toward the polymer bulk and/or parallel to the surface, while the CH2 moiety stands up on the PS surface. Our results indicate that the surface configuration changes do not require large length scale segmental motions or migration of macromolecules. Motions that are responsible for surface configuration changes could be relatively small rotational motions. The aging behaviors under different relative humidity conditions were shown to be similar from 18% to 91%, whereas the kinetics of surface polarity decays were faster in higher relative humidity. Here, the surface rearrangement of polystyrene films that were previously treated by oxygen plasma and aged, and was investigated in terms of contact angle after the water immersion. The contact angles of the water-immersed samples were found to change and approach the initial values before the immersion asymptotically.</description><subject>氧等离子体</subject><subject>聚苯乙烯</subject><subject>表面处理</subject><issn>0256-7679</issn><issn>1439-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNo1jEtOwzAARC0EEqVwAHYWC3YB24ntZGklThspnypJJbKKXNsphdDSpr0MZ-FOXIFWhcVoFu_NAHCP0RPGHnmuEKGMMx4gihAijF2AEfbcwGEEuZdgdMLOiV-Dm2F4Q4h5nPIR0NW8jEUoYSlFWYp8IjOZ1xUsYli8NBOZw1kqqkzA-ijUMoKzIm2quillLn--v-D_PGpykSVhBUUewek8S6KkbqCMYxnWt-CqU_1g7_56DOaxrMOpkxaTJBSpownDe8dwYxB2TYdcYqiPTMc4NoFnA46M4soutM-s5opgZIjLteJmYRW1zOedxp07Bo_n38_dZnuww779WA3a9r1a281haElAA0I8fhQfzqJ-3ayX29V62S6Ufu9WvW0xpT4_xv0FON1eVA</recordid><startdate>20050301</startdate><enddate>20050301</enddate><creator>Li, Junwei</creator><creator>Oh, Kyunghui</creator><creator>Yu, Hyuk</creator><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W92</scope><scope>~WA</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20050301</creationdate><title>SURFACE REARRANGEMENTS OF OXYGEN PLASMA TREATED POLYSTYRENE: SURFACE DYNAMICS AND HUMIDITY EFFECT</title><author>Li, Junwei ; Oh, Kyunghui ; Yu, Hyuk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c261t-d7dd013df032d580df671d94e970da7aebc86ec7a210d237ca7dbea5e687fc1f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>氧等离子体</topic><topic>聚苯乙烯</topic><topic>表面处理</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Junwei</creatorcontrib><creatorcontrib>Oh, Kyunghui</creatorcontrib><creatorcontrib>Yu, Hyuk</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-工程技术</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Chinese journal of polymer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Junwei</au><au>Oh, Kyunghui</au><au>Yu, Hyuk</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>SURFACE REARRANGEMENTS OF OXYGEN PLASMA TREATED POLYSTYRENE: SURFACE DYNAMICS AND HUMIDITY EFFECT</atitle><jtitle>Chinese journal of polymer science</jtitle><addtitle>Chinese Journal of Polymer Science</addtitle><date>2005-03-01</date><risdate>2005</risdate><volume>23</volume><issue>2</issue><spage>187</spage><epage>196</epage><pages>187-196</pages><issn>0256-7679</issn><eissn>1439-6203</eissn><abstract>The time evolution of oxygen plasma treated polystyrene (PS) surfaces was investigated upon storing them in the air under controlled humidity conditions. The methods of water contact angle, X-ray photoelectron spectroscopy (XPS), sum frequency generation (SFG) vibrational spectroscopy, and atomic force microscopy (AFM) were used to infer the surface properties and structure. Chemical groups containing oxygen were formed on the PS surface with the plasma treatment,demonstrated by water contact angle and XPS. The surface polarity decayed markedly on time, as assessed by steady increasein the water contact angle as a function of storage time, from zero to around 60°. The observed decay is interpreted as arising from surface rearrangement processes to burying polar groups away from the uppermost layer of the surfaces, which is in contact with air. On the other hand, XPS results show that the chemical composition in the first 3 nm surface layer is unaffected by the surface aging, and the depth profile of oxygen is essentially the same with time. A possible change of PS surface roughness was examined by AFM, and it showed that the increase of water contact angle during surface aging could not be attributed to surface roughness. Thus, it is concluded that surface aging is attributable to surface reorganization and the motion of oxygen containing groups is confined within the XPS probing depth. SFG spectroscopy, which is intrinsically interface-specific, was used to detect the chemical structure of PS surface at the molecular level after various aging times.The results are interpreted as follows. During the aging of the plasma treated PS surfaces, the oxygen containing groups undergo reorientation processes toward the polymer bulk and/or parallel to the surface, while the CH2 moiety stands up on the PS surface. Our results indicate that the surface configuration changes do not require large length scale segmental motions or migration of macromolecules. Motions that are responsible for surface configuration changes could be relatively small rotational motions. The aging behaviors under different relative humidity conditions were shown to be similar from 18% to 91%, whereas the kinetics of surface polarity decays were faster in higher relative humidity. Here, the surface rearrangement of polystyrene films that were previously treated by oxygen plasma and aged, and was investigated in terms of contact angle after the water immersion. The contact angles of the water-immersed samples were found to change and approach the initial values before the immersion asymptotically.</abstract><doi>10.1142/S0256767905000266</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0256-7679
ispartof Chinese journal of polymer science, 2005-03, Vol.23 (2), p.187-196
issn 0256-7679
1439-6203
language eng
recordid cdi_proquest_miscellaneous_29592247
source Alma/SFX Local Collection
subjects 氧等离子体
聚苯乙烯
表面处理
title SURFACE REARRANGEMENTS OF OXYGEN PLASMA TREATED POLYSTYRENE: SURFACE DYNAMICS AND HUMIDITY EFFECT
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T06%3A37%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_chong&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=SURFACE%20REARRANGEMENTS%20OF%20OXYGEN%20PLASMA%20TREATED%20POLYSTYRENE%EF%BC%9A%20SURFACE%20DYNAMICS%20AND%20HUMIDITY%20EFFECT&rft.jtitle=Chinese%20journal%20of%20polymer%20science&rft.au=Li,%20Junwei&rft.date=2005-03-01&rft.volume=23&rft.issue=2&rft.spage=187&rft.epage=196&rft.pages=187-196&rft.issn=0256-7679&rft.eissn=1439-6203&rft_id=info:doi/10.1142/S0256767905000266&rft_dat=%3Cproquest_chong%3E29592247%3C/proquest_chong%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=29592247&rft_id=info:pmid/&rft_cqvip_id=15587558&rfr_iscdi=true