Amphiphilic Block-Random Copolymers: Self-Folding Behavior and Stabilizers in Emulsion Polymerization
Polystyrene-b-[polystyrene-r-poly(acrylic acid)] block-random copolymers have been synthesized at various molecular weights (7000–23 200 g/mol) and with compositions between 6 and 39 mol % acrylic acid by nitroxide-mediated polymerization. Emulsion polymerizations of styrene stabilized by block-ran...
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Veröffentlicht in: | Macromolecules 2019-06, Vol.52 (12), p.4510-4519 |
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description | Polystyrene-b-[polystyrene-r-poly(acrylic acid)] block-random copolymers have been synthesized at various molecular weights (7000–23 200 g/mol) and with compositions between 6 and 39 mol % acrylic acid by nitroxide-mediated polymerization. Emulsion polymerizations of styrene stabilized by block-random copolymers yielded stable latexes at stabilizer concentrations ≥3 wt % based on monomer. A series of emulsion polymerizations with varying stabilizer content suggests that a novel nucleation mechanism occurs in block-random copolymer-stabilized emulsion polymerizations, exhibiting distinctly different behaviors from block copolymers or conventional small-molecule surfactants. Moreover, alkaline aqueous dispersions of the block-random copolymers were prepared with ease up to concentrations of 300 g/L, whereas similar block copolymers are limited to ∼1 g/L. Analysis of the dispersions via dynamic light scattering and atomic force microscopy suggests that single-chain nanoparticles form via a self-folding process with hydrodynamic diameters between 2.4 and 5 nm. The novel stabilizer structures may be tuned for rapid dispersion through their anchoring block [polystyrene] and high stabilization efficiency through the stabilizing block [polystyrene-r-poly(acrylic acid)]. |
doi_str_mv | 10.1021/acs.macromol.9b00519 |
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D ; Reck, Bernd ; Cunningham, Michael F</creator><creatorcontrib>Sanders, Connor A ; George, Sean R ; Deeter, Gary A ; Campbell, J. D ; Reck, Bernd ; Cunningham, Michael F</creatorcontrib><description>Polystyrene-b-[polystyrene-r-poly(acrylic acid)] block-random copolymers have been synthesized at various molecular weights (7000–23 200 g/mol) and with compositions between 6 and 39 mol % acrylic acid by nitroxide-mediated polymerization. Emulsion polymerizations of styrene stabilized by block-random copolymers yielded stable latexes at stabilizer concentrations ≥3 wt % based on monomer. A series of emulsion polymerizations with varying stabilizer content suggests that a novel nucleation mechanism occurs in block-random copolymer-stabilized emulsion polymerizations, exhibiting distinctly different behaviors from block copolymers or conventional small-molecule surfactants. Moreover, alkaline aqueous dispersions of the block-random copolymers were prepared with ease up to concentrations of 300 g/L, whereas similar block copolymers are limited to ∼1 g/L. Analysis of the dispersions via dynamic light scattering and atomic force microscopy suggests that single-chain nanoparticles form via a self-folding process with hydrodynamic diameters between 2.4 and 5 nm. 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Moreover, alkaline aqueous dispersions of the block-random copolymers were prepared with ease up to concentrations of 300 g/L, whereas similar block copolymers are limited to ∼1 g/L. Analysis of the dispersions via dynamic light scattering and atomic force microscopy suggests that single-chain nanoparticles form via a self-folding process with hydrodynamic diameters between 2.4 and 5 nm. The novel stabilizer structures may be tuned for rapid dispersion through their anchoring block [polystyrene] and high stabilization efficiency through the stabilizing block [polystyrene-r-poly(acrylic acid)].</description><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kMFKAzEQhoMoWKtv4CEvsHWSTXY33trSqlBQbO9Lks3a1GRTNq3QPr0prVdhYBjm_4bhQ-iRwIgAJU9Sx5GXug8-uJFQAJyIKzQgnELGq5xfowEAZZmgorxFdzFuAAjhLB8gM_bbtU3lrMYTF_R39im7Jng8DdvgDt708RkvjWuzeXCN7b7wxKzljw09Tjm83EmV2GOKYdvhmd-7aEOHP86sPcpdGu_RTStdNA-XPkSr-Ww1fc0W7y9v0_Eik7ngu0yAVlyRkohK8dLkUGquTNWYqpUtBxANoUq2piRMaCpyVhSM09IU1LSasnyI2PlsUhFjb9p621sv-0NNoD6ZqpOp-s9UfTGVMDhjp-0m7Psu_fg_8gu1HnJq</recordid><startdate>20190625</startdate><enddate>20190625</enddate><creator>Sanders, Connor A</creator><creator>George, Sean R</creator><creator>Deeter, Gary A</creator><creator>Campbell, J. D</creator><creator>Reck, Bernd</creator><creator>Cunningham, Michael F</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0001-8226-5990</orcidid></search><sort><creationdate>20190625</creationdate><title>Amphiphilic Block-Random Copolymers: Self-Folding Behavior and Stabilizers in Emulsion Polymerization</title><author>Sanders, Connor A ; George, Sean R ; Deeter, Gary A ; Campbell, J. D ; Reck, Bernd ; Cunningham, Michael F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a395t-90cb5b17198b57e307c5be8de8faf5009d12bafe7149c2934664527e62efc243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sanders, Connor A</creatorcontrib><creatorcontrib>George, Sean R</creatorcontrib><creatorcontrib>Deeter, Gary A</creatorcontrib><creatorcontrib>Campbell, J. D</creatorcontrib><creatorcontrib>Reck, Bernd</creatorcontrib><creatorcontrib>Cunningham, Michael F</creatorcontrib><collection>CrossRef</collection><jtitle>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sanders, Connor A</au><au>George, Sean R</au><au>Deeter, Gary A</au><au>Campbell, J. D</au><au>Reck, Bernd</au><au>Cunningham, Michael F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amphiphilic Block-Random Copolymers: Self-Folding Behavior and Stabilizers in Emulsion Polymerization</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>2019-06-25</date><risdate>2019</risdate><volume>52</volume><issue>12</issue><spage>4510</spage><epage>4519</epage><pages>4510-4519</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><abstract>Polystyrene-b-[polystyrene-r-poly(acrylic acid)] block-random copolymers have been synthesized at various molecular weights (7000–23 200 g/mol) and with compositions between 6 and 39 mol % acrylic acid by nitroxide-mediated polymerization. Emulsion polymerizations of styrene stabilized by block-random copolymers yielded stable latexes at stabilizer concentrations ≥3 wt % based on monomer. A series of emulsion polymerizations with varying stabilizer content suggests that a novel nucleation mechanism occurs in block-random copolymer-stabilized emulsion polymerizations, exhibiting distinctly different behaviors from block copolymers or conventional small-molecule surfactants. Moreover, alkaline aqueous dispersions of the block-random copolymers were prepared with ease up to concentrations of 300 g/L, whereas similar block copolymers are limited to ∼1 g/L. Analysis of the dispersions via dynamic light scattering and atomic force microscopy suggests that single-chain nanoparticles form via a self-folding process with hydrodynamic diameters between 2.4 and 5 nm. The novel stabilizer structures may be tuned for rapid dispersion through their anchoring block [polystyrene] and high stabilization efficiency through the stabilizing block [polystyrene-r-poly(acrylic acid)].</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.macromol.9b00519</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-8226-5990</orcidid></addata></record> |
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title | Amphiphilic Block-Random Copolymers: Self-Folding Behavior and Stabilizers in Emulsion Polymerization |
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