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Solution Properties of 1,3-Cyclohexadiene Polymers by Small Angle Neutron and Light Scattering
1,3-Cyclohexdiene polymers (PCHD) and their derivatives are of interest due to the six-member rings in the main chain, which are expected to impart higher mechanical strength and better thermal and chemical stability, as compared to common vinyl polymers. For example, hydrogenated PCHD has the highe...
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Published in: | Macromolecules 2006-01, Vol.39 (2) |
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creator | Yun, Seok I Melnichenko, Yuri B Wignall, George D Hong, Kunlun Mays, Jimmy Britt, Phillip F Terao, Ken Nakamura, Yo |
description | 1,3-Cyclohexdiene polymers (PCHD) and their derivatives are of interest due to the six-member rings in the main chain, which are expected to impart higher mechanical strength and better thermal and chemical stability, as compared to common vinyl polymers. For example, hydrogenated PCHD has the highest glass transition temperature (T{sub g} {approx} 231 C) of all hydrocarbon polymers, and it also shows good heat, weather, impact, abrasion, and chemical resistance as well as low water absorption. In addition, PCHD has unique photochemical properties, such as excellent transparency, due to the isolated double bonds in the main chain. Also, block copolymers containing PCHD show unusual phase separation behavior. For example, a styrene/1,3-CHD block copolymer (PS-b-PCHD) with 50 vol % CHD (1,4/1,2 {approx} 95/5) exhibits a core-shell or hollow cylinder morphology, while a typical styrene/acyclic diene (isoprene or butadiene) block copolymer with similar composition exhibits a lamellar structure. Such phase behavior and many other properties strongly depend on the conformation of the polymer in solution or bulk. However, almost no data have been reported on the conformation of PCHD, probably because of the lack of well-defined and well-characterized samples. Here we report solution properties of PCHD in tetrahydrofuran (THF) and chloroform by multiangle laser light scattering, viscometry, and small-angle neutron scattering (SANS). |
doi_str_mv | 10.1021/ma052022h |
format | article |
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For example, a styrene/1,3-CHD block copolymer (PS-b-PCHD) with 50 vol % CHD (1,4/1,2 {approx} 95/5) exhibits a core-shell or hollow cylinder morphology, while a typical styrene/acyclic diene (isoprene or butadiene) block copolymer with similar composition exhibits a lamellar structure. Such phase behavior and many other properties strongly depend on the conformation of the polymer in solution or bulk. However, almost no data have been reported on the conformation of PCHD, probably because of the lack of well-defined and well-characterized samples. 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(ORNL), Oak Ridge, TN (United States)</creatorcontrib><creatorcontrib>High Flux Isotope Reactor</creatorcontrib><title>Solution Properties of 1,3-Cyclohexadiene Polymers by Small Angle Neutron and Light Scattering</title><title>Macromolecules</title><description>1,3-Cyclohexdiene polymers (PCHD) and their derivatives are of interest due to the six-member rings in the main chain, which are expected to impart higher mechanical strength and better thermal and chemical stability, as compared to common vinyl polymers. For example, hydrogenated PCHD has the highest glass transition temperature (T{sub g} {approx} 231 C) of all hydrocarbon polymers, and it also shows good heat, weather, impact, abrasion, and chemical resistance as well as low water absorption. In addition, PCHD has unique photochemical properties, such as excellent transparency, due to the isolated double bonds in the main chain. Also, block copolymers containing PCHD show unusual phase separation behavior. For example, a styrene/1,3-CHD block copolymer (PS-b-PCHD) with 50 vol % CHD (1,4/1,2 {approx} 95/5) exhibits a core-shell or hollow cylinder morphology, while a typical styrene/acyclic diene (isoprene or butadiene) block copolymer with similar composition exhibits a lamellar structure. Such phase behavior and many other properties strongly depend on the conformation of the polymer in solution or bulk. However, almost no data have been reported on the conformation of PCHD, probably because of the lack of well-defined and well-characterized samples. Here we report solution properties of PCHD in tetrahydrofuran (THF) and chloroform by multiangle laser light scattering, viscometry, and small-angle neutron scattering (SANS).</description><subject>ABSORPTION</subject><subject>BUTADIENE</subject><subject>CHLOROFORM</subject><subject>COPOLYMERS</subject><subject>DIENES</subject><subject>DOUBLE BONDS</subject><subject>HYDROCARBONS</subject><subject>ISOPRENE</subject><subject>LASERS</subject><subject>LIGHT SCATTERING</subject><subject>MORPHOLOGY</subject><subject>NEUTRON DIFFRACTION</subject><subject>OPACITY</subject><subject>PHYSICS OF ELEMENTARY PARTICLES AND FIELDS</subject><subject>POLYMERS</subject><subject>SMALL ANGLE SCATTERING</subject><subject>SOLUTIONS</subject><subject>TETRAHYDROFURAN</subject><subject>TRANSITION TEMPERATURE</subject><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqNjMFqAjEUAENR6Fp76B88PHf1JXFp9yhS6UFE2J6VGJ-7KdmkJE_o_n09-AE9zRyGEeJF4lyikoveYKVQqe5BFPJmZfWuq5EoENWyrFX99igmOX8jSlktdSEOTfRXdjHAPsUfSuwoQ7yAfNXlerA-dvRrzo4CwT76oaeU4TRA0xvvYRVaT7CjK6fbwIQzbF3bMTTWMFNyoZ2K8cX4TM93PonZ5uNr_VnGzO6YrWOynY0hkOWjRNRK1_pf0R8yPEis</recordid><startdate>20060101</startdate><enddate>20060101</enddate><creator>Yun, Seok I</creator><creator>Melnichenko, Yuri B</creator><creator>Wignall, George D</creator><creator>Hong, Kunlun</creator><creator>Mays, Jimmy</creator><creator>Britt, Phillip F</creator><creator>Terao, Ken</creator><creator>Nakamura, Yo</creator><scope>OTOTI</scope></search><sort><creationdate>20060101</creationdate><title>Solution Properties of 1,3-Cyclohexadiene Polymers by Small Angle Neutron and Light Scattering</title><author>Yun, Seok I ; Melnichenko, Yuri B ; Wignall, George D ; Hong, Kunlun ; Mays, Jimmy ; Britt, Phillip F ; Terao, Ken ; Nakamura, Yo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-osti_scitechconnect_10032393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>ABSORPTION</topic><topic>BUTADIENE</topic><topic>CHLOROFORM</topic><topic>COPOLYMERS</topic><topic>DIENES</topic><topic>DOUBLE BONDS</topic><topic>HYDROCARBONS</topic><topic>ISOPRENE</topic><topic>LASERS</topic><topic>LIGHT SCATTERING</topic><topic>MORPHOLOGY</topic><topic>NEUTRON DIFFRACTION</topic><topic>OPACITY</topic><topic>PHYSICS OF ELEMENTARY PARTICLES AND FIELDS</topic><topic>POLYMERS</topic><topic>SMALL ANGLE SCATTERING</topic><topic>SOLUTIONS</topic><topic>TETRAHYDROFURAN</topic><topic>TRANSITION TEMPERATURE</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yun, Seok I</creatorcontrib><creatorcontrib>Melnichenko, Yuri B</creatorcontrib><creatorcontrib>Wignall, George D</creatorcontrib><creatorcontrib>Hong, Kunlun</creatorcontrib><creatorcontrib>Mays, Jimmy</creatorcontrib><creatorcontrib>Britt, Phillip F</creatorcontrib><creatorcontrib>Terao, Ken</creatorcontrib><creatorcontrib>Nakamura, Yo</creatorcontrib><creatorcontrib>Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)</creatorcontrib><creatorcontrib>High Flux Isotope Reactor</creatorcontrib><collection>OSTI.GOV</collection><jtitle>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yun, Seok I</au><au>Melnichenko, Yuri B</au><au>Wignall, George D</au><au>Hong, Kunlun</au><au>Mays, Jimmy</au><au>Britt, Phillip F</au><au>Terao, Ken</au><au>Nakamura, Yo</au><aucorp>Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)</aucorp><aucorp>High Flux Isotope Reactor</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Solution Properties of 1,3-Cyclohexadiene Polymers by Small Angle Neutron and Light Scattering</atitle><jtitle>Macromolecules</jtitle><date>2006-01-01</date><risdate>2006</risdate><volume>39</volume><issue>2</issue><issn>0024-9297</issn><eissn>1520-5835</eissn><abstract>1,3-Cyclohexdiene polymers (PCHD) and their derivatives are of interest due to the six-member rings in the main chain, which are expected to impart higher mechanical strength and better thermal and chemical stability, as compared to common vinyl polymers. For example, hydrogenated PCHD has the highest glass transition temperature (T{sub g} {approx} 231 C) of all hydrocarbon polymers, and it also shows good heat, weather, impact, abrasion, and chemical resistance as well as low water absorption. In addition, PCHD has unique photochemical properties, such as excellent transparency, due to the isolated double bonds in the main chain. Also, block copolymers containing PCHD show unusual phase separation behavior. For example, a styrene/1,3-CHD block copolymer (PS-b-PCHD) with 50 vol % CHD (1,4/1,2 {approx} 95/5) exhibits a core-shell or hollow cylinder morphology, while a typical styrene/acyclic diene (isoprene or butadiene) block copolymer with similar composition exhibits a lamellar structure. Such phase behavior and many other properties strongly depend on the conformation of the polymer in solution or bulk. However, almost no data have been reported on the conformation of PCHD, probably because of the lack of well-defined and well-characterized samples. Here we report solution properties of PCHD in tetrahydrofuran (THF) and chloroform by multiangle laser light scattering, viscometry, and small-angle neutron scattering (SANS).</abstract><cop>United States</cop><doi>10.1021/ma052022h</doi></addata></record> |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | ABSORPTION BUTADIENE CHLOROFORM COPOLYMERS DIENES DOUBLE BONDS HYDROCARBONS ISOPRENE LASERS LIGHT SCATTERING MORPHOLOGY NEUTRON DIFFRACTION OPACITY PHYSICS OF ELEMENTARY PARTICLES AND FIELDS POLYMERS SMALL ANGLE SCATTERING SOLUTIONS TETRAHYDROFURAN TRANSITION TEMPERATURE |
title | Solution Properties of 1,3-Cyclohexadiene Polymers by Small Angle Neutron and Light Scattering |
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