Pure gas and vapor permeation properties of poly[1-phenyl-2-[ p-(trimethylsilyl)phenyl]acetylene] (PTMSDPA) and its desilylated analog, poly[diphenylacetylene] (PDPA)
The permeabilities of He, H 2, N 2, O 2, CO 2, CH 4, C 2H 6, C 3H 8, and n-C 4H 10 in poly[1-phenyl-2-[ p-(trimethylsilyl)phenyl]acetylene] (PTMSDPA) and poly[diphenylacetylene] (PDPA) are presented and compared to those of poly(1-trimethylsilyl-1-propyne) (PTMSP), poly(1-phenyl-1-propyne) (PPP), an...
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container_title | Polymer (Guilford) |
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creator | Raharjo, Roy D. Lee, Hyuck J. Freeman, Benny D. Sakaguchi, Toshikazu Masuda, Toshio |
description | The permeabilities of He, H
2, N
2, O
2, CO
2, CH
4, C
2H
6, C
3H
8, and
n-C
4H
10 in poly[1-phenyl-2-[
p-(trimethylsilyl)phenyl]acetylene] (PTMSDPA) and poly[diphenylacetylene] (PDPA) are presented and compared to those of poly(1-trimethylsilyl-1-propyne) (PTMSP), poly(1-phenyl-1-propyne) (PPP), and polysulfone. Like PTMSP, PTMSDPA, a disubstituted glassy acetylene-based polymer, exhibits higher permeabilities to organic vapors than to permanent gases due to its rigid polyacetylene backbone and bulky side groups, which provide a relatively high fractional free volume (FFV) value of 0.26. Desilylation was performed on PTMSDPA. The resulting material, PDPA, is totally insoluble in common organic solvents, so it has much higher chemical resistance than PTMSDPA. Additionally, due to its insolubility in polymerization solvents, desilylation provides the only known route to high molar mass PDPA. The FFV of the resulting membrane (PDPA) is reduced by approximately 12% relative to that of PTMSDPA. This leads to a decrease in gas permeability values and selectivity of organic vapors relative to nitrogen. For example, the oxygen permeability is reduced from 1200 to 500 Barrers upon desilylation. The pure gas selectivities decrease from 9 to 3 for
n-C
4H
10/N
2 and from 26 to 9 for C
3H
8/N
2. |
doi_str_mv | 10.1016/j.polymer.2005.05.093 |
format | Article |
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2, N
2, O
2, CO
2, CH
4, C
2H
6, C
3H
8, and
n-C
4H
10 in poly[1-phenyl-2-[
p-(trimethylsilyl)phenyl]acetylene] (PTMSDPA) and poly[diphenylacetylene] (PDPA) are presented and compared to those of poly(1-trimethylsilyl-1-propyne) (PTMSP), poly(1-phenyl-1-propyne) (PPP), and polysulfone. Like PTMSP, PTMSDPA, a disubstituted glassy acetylene-based polymer, exhibits higher permeabilities to organic vapors than to permanent gases due to its rigid polyacetylene backbone and bulky side groups, which provide a relatively high fractional free volume (FFV) value of 0.26. Desilylation was performed on PTMSDPA. The resulting material, PDPA, is totally insoluble in common organic solvents, so it has much higher chemical resistance than PTMSDPA. Additionally, due to its insolubility in polymerization solvents, desilylation provides the only known route to high molar mass PDPA. The FFV of the resulting membrane (PDPA) is reduced by approximately 12% relative to that of PTMSDPA. This leads to a decrease in gas permeability values and selectivity of organic vapors relative to nitrogen. For example, the oxygen permeability is reduced from 1200 to 500 Barrers upon desilylation. The pure gas selectivities decrease from 9 to 3 for
n-C
4H
10/N
2 and from 26 to 9 for C
3H
8/N
2.</description><identifier>ISSN: 0032-3861</identifier><identifier>EISSN: 1873-2291</identifier><identifier>DOI: 10.1016/j.polymer.2005.05.093</identifier><identifier>CODEN: POLMAG</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Applied sciences ; Exact sciences and technology ; Miscellaneous ; Organic polymers ; Permeability ; Physicochemistry of polymers ; Poly[1-phenyl-2-[ p-(trimethylsilyl)phenyl]acetylene] ; Poly[diphenylacetylene] ; Properties and characterization</subject><ispartof>Polymer (Guilford), 2005-08, Vol.46 (17), p.6316-6324</ispartof><rights>2005 Elsevier Ltd</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-ebdeb4e0c9b33d46b84e0b1bfefecfd6f0d1e425c2d7f497b9a5b7daa78dcd603</citedby><cites>FETCH-LOGICAL-c511t-ebdeb4e0c9b33d46b84e0b1bfefecfd6f0d1e425c2d7f497b9a5b7daa78dcd603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.polymer.2005.05.093$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16987766$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Raharjo, Roy D.</creatorcontrib><creatorcontrib>Lee, Hyuck J.</creatorcontrib><creatorcontrib>Freeman, Benny D.</creatorcontrib><creatorcontrib>Sakaguchi, Toshikazu</creatorcontrib><creatorcontrib>Masuda, Toshio</creatorcontrib><title>Pure gas and vapor permeation properties of poly[1-phenyl-2-[ p-(trimethylsilyl)phenyl]acetylene] (PTMSDPA) and its desilylated analog, poly[diphenylacetylene] (PDPA)</title><title>Polymer (Guilford)</title><description>The permeabilities of He, H
2, N
2, O
2, CO
2, CH
4, C
2H
6, C
3H
8, and
n-C
4H
10 in poly[1-phenyl-2-[
p-(trimethylsilyl)phenyl]acetylene] (PTMSDPA) and poly[diphenylacetylene] (PDPA) are presented and compared to those of poly(1-trimethylsilyl-1-propyne) (PTMSP), poly(1-phenyl-1-propyne) (PPP), and polysulfone. Like PTMSP, PTMSDPA, a disubstituted glassy acetylene-based polymer, exhibits higher permeabilities to organic vapors than to permanent gases due to its rigid polyacetylene backbone and bulky side groups, which provide a relatively high fractional free volume (FFV) value of 0.26. Desilylation was performed on PTMSDPA. The resulting material, PDPA, is totally insoluble in common organic solvents, so it has much higher chemical resistance than PTMSDPA. Additionally, due to its insolubility in polymerization solvents, desilylation provides the only known route to high molar mass PDPA. The FFV of the resulting membrane (PDPA) is reduced by approximately 12% relative to that of PTMSDPA. This leads to a decrease in gas permeability values and selectivity of organic vapors relative to nitrogen. For example, the oxygen permeability is reduced from 1200 to 500 Barrers upon desilylation. The pure gas selectivities decrease from 9 to 3 for
n-C
4H
10/N
2 and from 26 to 9 for C
3H
8/N
2.</description><subject>Applied sciences</subject><subject>Exact sciences and technology</subject><subject>Miscellaneous</subject><subject>Organic polymers</subject><subject>Permeability</subject><subject>Physicochemistry of polymers</subject><subject>Poly[1-phenyl-2-[ p-(trimethylsilyl)phenyl]acetylene]</subject><subject>Poly[diphenylacetylene]</subject><subject>Properties and characterization</subject><issn>0032-3861</issn><issn>1873-2291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqNkd1q3DAQhU1podu0j1DQTUsC9UY_tmxflZD-BRK60PQqBCFLo0SL1nIlbcAv1OesHC-EXrUwIEb6zjlopijeErwmmPDT7Xr0btpBWFOM6_VcHXtWrEjbsJLSjjwvVhgzWrKWk5fFqxi3GGNa02pV_N7sA6A7GZEcNHqQow9ohLADmawf0Bh87pKFiLxBc8wNKcd7GCZX0vIGjeVxCnYH6X5y0brJnSyPt1JBmhwMcIuON9dXPz5tzk4eI2yKSMMjKxPofCedv_uweGu7yP9Sz9LXxQsjXYQ3h_Oo-Pnl8_X5t_Ly-9eL87PLUtWEpBJ6DX0FWHU9Y7rifZubnvQGDCijucGaQEVrRXVjqq7pO1n3jZayabXSHLOj4v3imz_-aw8xiZ2NCpyTA_h9FLRtOCWk_g-QY8pol8F6AVXwMQYwYswDk2ESBIt5fWIrDusT8_rEXB3LuneHABmVdCbIQdn4JOZd2zScZ-7jwkEey4PNLlFZGBRoG0Alob39R9IfyxW34g</recordid><startdate>20050808</startdate><enddate>20050808</enddate><creator>Raharjo, Roy D.</creator><creator>Lee, Hyuck J.</creator><creator>Freeman, Benny D.</creator><creator>Sakaguchi, Toshikazu</creator><creator>Masuda, Toshio</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SE</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope><scope>F28</scope><scope>FR3</scope></search><sort><creationdate>20050808</creationdate><title>Pure gas and vapor permeation properties of poly[1-phenyl-2-[ p-(trimethylsilyl)phenyl]acetylene] (PTMSDPA) and its desilylated analog, poly[diphenylacetylene] (PDPA)</title><author>Raharjo, Roy D. ; Lee, Hyuck J. ; Freeman, Benny D. ; Sakaguchi, Toshikazu ; Masuda, Toshio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c511t-ebdeb4e0c9b33d46b84e0b1bfefecfd6f0d1e425c2d7f497b9a5b7daa78dcd603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Applied sciences</topic><topic>Exact sciences and technology</topic><topic>Miscellaneous</topic><topic>Organic polymers</topic><topic>Permeability</topic><topic>Physicochemistry of polymers</topic><topic>Poly[1-phenyl-2-[ p-(trimethylsilyl)phenyl]acetylene]</topic><topic>Poly[diphenylacetylene]</topic><topic>Properties and characterization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Raharjo, Roy D.</creatorcontrib><creatorcontrib>Lee, Hyuck J.</creatorcontrib><creatorcontrib>Freeman, Benny D.</creatorcontrib><creatorcontrib>Sakaguchi, Toshikazu</creatorcontrib><creatorcontrib>Masuda, Toshio</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Corrosion Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><jtitle>Polymer (Guilford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Raharjo, Roy D.</au><au>Lee, Hyuck J.</au><au>Freeman, Benny D.</au><au>Sakaguchi, Toshikazu</au><au>Masuda, Toshio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pure gas and vapor permeation properties of poly[1-phenyl-2-[ p-(trimethylsilyl)phenyl]acetylene] (PTMSDPA) and its desilylated analog, poly[diphenylacetylene] (PDPA)</atitle><jtitle>Polymer (Guilford)</jtitle><date>2005-08-08</date><risdate>2005</risdate><volume>46</volume><issue>17</issue><spage>6316</spage><epage>6324</epage><pages>6316-6324</pages><issn>0032-3861</issn><eissn>1873-2291</eissn><coden>POLMAG</coden><abstract>The permeabilities of He, H
2, N
2, O
2, CO
2, CH
4, C
2H
6, C
3H
8, and
n-C
4H
10 in poly[1-phenyl-2-[
p-(trimethylsilyl)phenyl]acetylene] (PTMSDPA) and poly[diphenylacetylene] (PDPA) are presented and compared to those of poly(1-trimethylsilyl-1-propyne) (PTMSP), poly(1-phenyl-1-propyne) (PPP), and polysulfone. Like PTMSP, PTMSDPA, a disubstituted glassy acetylene-based polymer, exhibits higher permeabilities to organic vapors than to permanent gases due to its rigid polyacetylene backbone and bulky side groups, which provide a relatively high fractional free volume (FFV) value of 0.26. Desilylation was performed on PTMSDPA. The resulting material, PDPA, is totally insoluble in common organic solvents, so it has much higher chemical resistance than PTMSDPA. Additionally, due to its insolubility in polymerization solvents, desilylation provides the only known route to high molar mass PDPA. The FFV of the resulting membrane (PDPA) is reduced by approximately 12% relative to that of PTMSDPA. This leads to a decrease in gas permeability values and selectivity of organic vapors relative to nitrogen. For example, the oxygen permeability is reduced from 1200 to 500 Barrers upon desilylation. The pure gas selectivities decrease from 9 to 3 for
n-C
4H
10/N
2 and from 26 to 9 for C
3H
8/N
2.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.polymer.2005.05.093</doi><tpages>9</tpages></addata></record> |
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subjects | Applied sciences Exact sciences and technology Miscellaneous Organic polymers Permeability Physicochemistry of polymers Poly[1-phenyl-2-[ p-(trimethylsilyl)phenyl]acetylene] Poly[diphenylacetylene] Properties and characterization |
title | Pure gas and vapor permeation properties of poly[1-phenyl-2-[ p-(trimethylsilyl)phenyl]acetylene] (PTMSDPA) and its desilylated analog, poly[diphenylacetylene] (PDPA) |
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