Tunable phase transition behaviors of pH-sensitive polyaspartamides having various cationic pendant groups
New pH-sensitive graft copolymers based on poly(2-hydroxyethyl aspartamide) (PHEA) were prepared by attaching various cationic monomers, such as 4-(aminomethyl)pyridine (PY), 1-(3-aminopropyl)imidazole (IM), and N-(3-aminopropyl)dibuthylamine (BU), as pH-sensitive units and octadecylamine (C₁₈) as a...
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Veröffentlicht in: | Colloid and polymer science 2009-08, Vol.287 (8), p.919-926 |
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description | New pH-sensitive graft copolymers based on poly(2-hydroxyethyl aspartamide) (PHEA) were prepared by attaching various cationic monomers, such as 4-(aminomethyl)pyridine (PY), 1-(3-aminopropyl)imidazole (IM), and N-(3-aminopropyl)dibuthylamine (BU), as pH-sensitive units and octadecylamine (C₁₈) as a hydrophobic segment on poly(succinimide). Phase transition of each copolymer solution occurred at a vicinity of the pK a value of the cationic groups, and their insoluble pH ranges were broadened as the feed amount of pH-sensitive moieties was increased. Depending on the cationic grafts having different pK a values, the pH ranges where the copolymer became insoluble could be tuned. Copolymers PHEA-g-C₁₈-PY, PHEA-g-C₁₈-IM, and PHEA-g-C₁₈-BU exhibited phase separations in solutions at pH ranges of 4~6, 6~8, and 9~12, respectively. These polymers have the unique feature of their pH sensitivity profiles being identified to three regimes. Under low pH conditions (below pK a ), the polymer solution is transparent. At medium pH (around pK a ), polymer precipitation occurred in solution. At pH > pK a , the polymer solution is gradually dissolved again. |
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Phase transition of each copolymer solution occurred at a vicinity of the pK a value of the cationic groups, and their insoluble pH ranges were broadened as the feed amount of pH-sensitive moieties was increased. Depending on the cationic grafts having different pK a values, the pH ranges where the copolymer became insoluble could be tuned. Copolymers PHEA-g-C₁₈-PY, PHEA-g-C₁₈-IM, and PHEA-g-C₁₈-BU exhibited phase separations in solutions at pH ranges of 4~6, 6~8, and 9~12, respectively. These polymers have the unique feature of their pH sensitivity profiles being identified to three regimes. Under low pH conditions (below pK a ), the polymer solution is transparent. At medium pH (around pK a ), polymer precipitation occurred in solution. At pH > pK a , the polymer solution is gradually dissolved again.</description><identifier>ISSN: 0303-402X</identifier><identifier>EISSN: 1435-1536</identifier><identifier>DOI: 10.1007/s00396-009-2046-8</identifier><identifier>CODEN: CPMSB6</identifier><language>eng</language><publisher>Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag</publisher><subject>Aminoacid polymers ; Applied sciences ; Cationic ; Characterization and Evaluation of Materials ; Chemistry ; Chemistry and Materials Science ; Complex Fluids and Microfluidics ; Copolymers ; Exact sciences and technology ; Food Science ; Graft copolymers ; Monomers ; Nanotechnology and Microengineering ; Original Contribution ; Phase transformations ; Physical Chemistry ; Physicochemistry of polymers ; Polymer Sciences ; Precipitation ; Segments ; Soft and Granular Matter ; Synthetic biopolymers</subject><ispartof>Colloid and polymer science, 2009-08, Vol.287 (8), p.919-926</ispartof><rights>Springer-Verlag 2009</rights><rights>2009 INIST-CNRS</rights><rights>Colloid and Polymer Science is a copyright of Springer, 2009.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-a949948d6b05c9370be37ef167838babbff7265ffff6302e1e1b3d31cea914a93</citedby><cites>FETCH-LOGICAL-c402t-a949948d6b05c9370be37ef167838babbff7265ffff6302e1e1b3d31cea914a93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00396-009-2046-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00396-009-2046-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21699799$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Han Woong</creatorcontrib><creatorcontrib>Jin, Hye-Seung</creatorcontrib><creatorcontrib>Yang, Sung Yun</creatorcontrib><creatorcontrib>Kim, Jong-Duk</creatorcontrib><title>Tunable phase transition behaviors of pH-sensitive polyaspartamides having various cationic pendant groups</title><title>Colloid and polymer science</title><addtitle>Colloid Polym Sci</addtitle><description>New pH-sensitive graft copolymers based on poly(2-hydroxyethyl aspartamide) (PHEA) were prepared by attaching various cationic monomers, such as 4-(aminomethyl)pyridine (PY), 1-(3-aminopropyl)imidazole (IM), and N-(3-aminopropyl)dibuthylamine (BU), as pH-sensitive units and octadecylamine (C₁₈) as a hydrophobic segment on poly(succinimide). Phase transition of each copolymer solution occurred at a vicinity of the pK a value of the cationic groups, and their insoluble pH ranges were broadened as the feed amount of pH-sensitive moieties was increased. Depending on the cationic grafts having different pK a values, the pH ranges where the copolymer became insoluble could be tuned. Copolymers PHEA-g-C₁₈-PY, PHEA-g-C₁₈-IM, and PHEA-g-C₁₈-BU exhibited phase separations in solutions at pH ranges of 4~6, 6~8, and 9~12, respectively. These polymers have the unique feature of their pH sensitivity profiles being identified to three regimes. Under low pH conditions (below pK a ), the polymer solution is transparent. At medium pH (around pK a ), polymer precipitation occurred in solution. At pH > pK a , the polymer solution is gradually dissolved again.</description><subject>Aminoacid polymers</subject><subject>Applied sciences</subject><subject>Cationic</subject><subject>Characterization and Evaluation of Materials</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Complex Fluids and Microfluidics</subject><subject>Copolymers</subject><subject>Exact sciences and technology</subject><subject>Food Science</subject><subject>Graft copolymers</subject><subject>Monomers</subject><subject>Nanotechnology and Microengineering</subject><subject>Original Contribution</subject><subject>Phase transformations</subject><subject>Physical Chemistry</subject><subject>Physicochemistry of polymers</subject><subject>Polymer Sciences</subject><subject>Precipitation</subject><subject>Segments</subject><subject>Soft and Granular Matter</subject><subject>Synthetic biopolymers</subject><issn>0303-402X</issn><issn>1435-1536</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp9kcFq3DAQhkVpoNttHiCnCkrpye1IsmXrWELaBAI9NIHcxFgrb7x4JVdjL-TtK9ehlB6iiw7zzc_PN4xdCPgsAOovBKCMLgBMIaHURfOKbUSpqkJUSr9mG1CgihLkwxv2lugAAKXResMOd3PAdvB8fETyfEoYqJ_6GHjrH_HUx0Q8dny8Lsj_mZwyGocnpBHThMd-54kvYNjzE6Y-zsQdLgG946MPOwwT36c4j_SOnXU4kD9__rfs_tvV3eV1cfvj-83l19vC5X5TgaY0pmx2uoXKGVVD61XtO6HrRjUttm3X1VJXXX5agfTCi1btlHAejSjRqC37tOaOKf6aPU322JPzw4DB53rWCGMqUWc7W_bhP_IQ5xRyOSuaWlZGlVJmSqyUS5Eo-c6OqT9ierIC7CLfrvJtlm8X-bbJOx-fk5EcDl3W6nr6uyiFNqY2S1e5cpRHYe_TPw1eCH-_LnUYLe5TDr7_KUEoELpSVb70b19Zn1I</recordid><startdate>20090801</startdate><enddate>20090801</enddate><creator>Park, Han Woong</creator><creator>Jin, Hye-Seung</creator><creator>Yang, Sung Yun</creator><creator>Kim, Jong-Duk</creator><general>Berlin/Heidelberg : Springer-Verlag</general><general>Springer-Verlag</general><general>Springer</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope></search><sort><creationdate>20090801</creationdate><title>Tunable phase transition behaviors of pH-sensitive polyaspartamides having various cationic pendant groups</title><author>Park, Han Woong ; Jin, Hye-Seung ; Yang, Sung Yun ; Kim, Jong-Duk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-a949948d6b05c9370be37ef167838babbff7265ffff6302e1e1b3d31cea914a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Aminoacid polymers</topic><topic>Applied sciences</topic><topic>Cationic</topic><topic>Characterization and Evaluation of Materials</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Complex Fluids and Microfluidics</topic><topic>Copolymers</topic><topic>Exact sciences and technology</topic><topic>Food Science</topic><topic>Graft copolymers</topic><topic>Monomers</topic><topic>Nanotechnology and Microengineering</topic><topic>Original Contribution</topic><topic>Phase transformations</topic><topic>Physical Chemistry</topic><topic>Physicochemistry of polymers</topic><topic>Polymer Sciences</topic><topic>Precipitation</topic><topic>Segments</topic><topic>Soft and Granular Matter</topic><topic>Synthetic biopolymers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Han Woong</creatorcontrib><creatorcontrib>Jin, Hye-Seung</creatorcontrib><creatorcontrib>Yang, Sung Yun</creatorcontrib><creatorcontrib>Kim, Jong-Duk</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><jtitle>Colloid and polymer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Han Woong</au><au>Jin, Hye-Seung</au><au>Yang, Sung Yun</au><au>Kim, Jong-Duk</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tunable phase transition behaviors of pH-sensitive polyaspartamides having various cationic pendant groups</atitle><jtitle>Colloid and polymer science</jtitle><stitle>Colloid Polym Sci</stitle><date>2009-08-01</date><risdate>2009</risdate><volume>287</volume><issue>8</issue><spage>919</spage><epage>926</epage><pages>919-926</pages><issn>0303-402X</issn><eissn>1435-1536</eissn><coden>CPMSB6</coden><abstract>New pH-sensitive graft copolymers based on poly(2-hydroxyethyl aspartamide) (PHEA) were prepared by attaching various cationic monomers, such as 4-(aminomethyl)pyridine (PY), 1-(3-aminopropyl)imidazole (IM), and N-(3-aminopropyl)dibuthylamine (BU), as pH-sensitive units and octadecylamine (C₁₈) as a hydrophobic segment on poly(succinimide). Phase transition of each copolymer solution occurred at a vicinity of the pK a value of the cationic groups, and their insoluble pH ranges were broadened as the feed amount of pH-sensitive moieties was increased. Depending on the cationic grafts having different pK a values, the pH ranges where the copolymer became insoluble could be tuned. Copolymers PHEA-g-C₁₈-PY, PHEA-g-C₁₈-IM, and PHEA-g-C₁₈-BU exhibited phase separations in solutions at pH ranges of 4~6, 6~8, and 9~12, respectively. These polymers have the unique feature of their pH sensitivity profiles being identified to three regimes. Under low pH conditions (below pK a ), the polymer solution is transparent. At medium pH (around pK a ), polymer precipitation occurred in solution. At pH > pK a , the polymer solution is gradually dissolved again.</abstract><cop>Berlin/Heidelberg</cop><pub>Berlin/Heidelberg : Springer-Verlag</pub><doi>10.1007/s00396-009-2046-8</doi><tpages>8</tpages></addata></record> |
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subjects | Aminoacid polymers Applied sciences Cationic Characterization and Evaluation of Materials Chemistry Chemistry and Materials Science Complex Fluids and Microfluidics Copolymers Exact sciences and technology Food Science Graft copolymers Monomers Nanotechnology and Microengineering Original Contribution Phase transformations Physical Chemistry Physicochemistry of polymers Polymer Sciences Precipitation Segments Soft and Granular Matter Synthetic biopolymers |
title | Tunable phase transition behaviors of pH-sensitive polyaspartamides having various cationic pendant groups |
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