Synthesis and properties of side chain fluorinated polyurethanes and evaluation of changes in microphase separation
•This study successfully prepared a side chain fluorinated chain extender and introduced into polyurethane.•19F NMR, 19F-19F NMR successfully resolved and determined the structure of fluorinated chain extender.•Calculate the degree of microphase separation of AMPF/PUs by FTIR curve fitting.•Side cha...
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description | •This study successfully prepared a side chain fluorinated chain extender and introduced into polyurethane.•19F NMR, 19F-19F NMR successfully resolved and determined the structure of fluorinated chain extender.•Calculate the degree of microphase separation of AMPF/PUs by FTIR curve fitting.•Side chain fluorinated chain extender can effectively improve the mechanical properties of polyurethane.
To develop marketable new waterproof and breathable membranes, this study successfully applied a simple synthesis method to combine pentadecafluorooctanoyl chloride and 2-Amino-2-methyl-1,3-propanediol into a novel long-segment side-chain fluorinated chain extender (AMPF), the structure was examined using nuclear magnetic resonance (NMR) spectroscopy. To promote environmental-friendliness, biodegradable polycaprolactone (PCL) was chosen to supply the soft segment of polyurethane (PU), methylene diphenyl diisocyanate to supply the hard segment, The successful introduction of AMPF into the PCL-based PU enabled the production of AMPF/PUs. To investigate the effect of AMPF on PCL-based PU, NMR and gel permeation chromatography were performed for the preliminary analysis of AMPF/PUs; curve fitting was applied in Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. The atomic force microscopy to determine the difference in van der Waals forces and microphase separation in AMPF/PUs; a thermal gravimetric analysis and dynamic mechanical analysis were conducted to determine the thermal properties of AMPF/PUs, and tensile test were conducted to determine the mechanical properties of AMPF/PUs. The results reveal that AMPF/PUs have a high degree of microphase separation, and the heat resistance of AMPF/PUs can be improved by 4–5 %, while the tensile strength can be increased by about 28 MPa with the increase of AMPF content. From the contact angle test, it is known that the increase of AMPF content can convert the hydrophilic polyurethane (77.8 ± 2.7°) into the hydrophobic (95.2 ± 2.1°) polyurethane. Therefore, it is shown that AMPF can not only improve the strength of polyurethane but also provide hydrophobic properties. This fluorinated chain extender shows considerable potential for the coatings materials and waterproof and breathable fabrics. |
doi_str_mv | 10.1016/j.porgcoat.2020.105702 |
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To develop marketable new waterproof and breathable membranes, this study successfully applied a simple synthesis method to combine pentadecafluorooctanoyl chloride and 2-Amino-2-methyl-1,3-propanediol into a novel long-segment side-chain fluorinated chain extender (AMPF), the structure was examined using nuclear magnetic resonance (NMR) spectroscopy. To promote environmental-friendliness, biodegradable polycaprolactone (PCL) was chosen to supply the soft segment of polyurethane (PU), methylene diphenyl diisocyanate to supply the hard segment, The successful introduction of AMPF into the PCL-based PU enabled the production of AMPF/PUs. To investigate the effect of AMPF on PCL-based PU, NMR and gel permeation chromatography were performed for the preliminary analysis of AMPF/PUs; curve fitting was applied in Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. The atomic force microscopy to determine the difference in van der Waals forces and microphase separation in AMPF/PUs; a thermal gravimetric analysis and dynamic mechanical analysis were conducted to determine the thermal properties of AMPF/PUs, and tensile test were conducted to determine the mechanical properties of AMPF/PUs. The results reveal that AMPF/PUs have a high degree of microphase separation, and the heat resistance of AMPF/PUs can be improved by 4–5 %, while the tensile strength can be increased by about 28 MPa with the increase of AMPF content. From the contact angle test, it is known that the increase of AMPF content can convert the hydrophilic polyurethane (77.8 ± 2.7°) into the hydrophobic (95.2 ± 2.1°) polyurethane. Therefore, it is shown that AMPF can not only improve the strength of polyurethane but also provide hydrophobic properties. This fluorinated chain extender shows considerable potential for the coatings materials and waterproof and breathable fabrics.</description><identifier>ISSN: 0300-9440</identifier><identifier>EISSN: 1873-331X</identifier><identifier>DOI: 10.1016/j.porgcoat.2020.105702</identifier><language>eng</language><publisher>Lausanne: Elsevier B.V</publisher><subject>19F-19F NMR ; Atomic beam spectroscopy ; Atomic force microscopy ; Biodegradability ; Chains ; Contact angle ; Curve fitting ; Diisocyanates ; Dynamic mechanical analysis ; Fluorinated ; Fluorination ; Gravimetric analysis ; Heat resistance ; Hydrophobicity ; Liquid chromatography ; MDI derived polyurethane ; Mechanical properties ; Microphase separation ; NMR ; NMR spectroscopy ; Nuclear magnetic resonance ; Photoelectrons ; Polycaprolactone ; Polyurethane ; Polyurethane resins ; Separation ; Spectrum analysis ; Synthesis ; Tensile strength ; Tensile tests ; Thermal resistance ; Thermodynamic properties ; Van der Waals forces</subject><ispartof>Progress in organic coatings, 2020-08, Vol.145, p.105702, Article 105702</ispartof><rights>2020 Elsevier B.V.</rights><rights>Copyright Elsevier BV Aug 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c340t-f09e0f810cab5a4f15fee46556b0f10bd936f193c7db0349d1516934223e84983</citedby><cites>FETCH-LOGICAL-c340t-f09e0f810cab5a4f15fee46556b0f10bd936f193c7db0349d1516934223e84983</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0300944019315152$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids></links><search><creatorcontrib>Li, Jia-Wun</creatorcontrib><creatorcontrib>Tsai, Hui-An</creatorcontrib><creatorcontrib>Lee, Hsun-Tsing</creatorcontrib><creatorcontrib>Cheng, Yung-Hsin</creatorcontrib><creatorcontrib>Chiu, Chih-Wei</creatorcontrib><creatorcontrib>Suen, Maw-Cherng</creatorcontrib><title>Synthesis and properties of side chain fluorinated polyurethanes and evaluation of changes in microphase separation</title><title>Progress in organic coatings</title><description>•This study successfully prepared a side chain fluorinated chain extender and introduced into polyurethane.•19F NMR, 19F-19F NMR successfully resolved and determined the structure of fluorinated chain extender.•Calculate the degree of microphase separation of AMPF/PUs by FTIR curve fitting.•Side chain fluorinated chain extender can effectively improve the mechanical properties of polyurethane.
To develop marketable new waterproof and breathable membranes, this study successfully applied a simple synthesis method to combine pentadecafluorooctanoyl chloride and 2-Amino-2-methyl-1,3-propanediol into a novel long-segment side-chain fluorinated chain extender (AMPF), the structure was examined using nuclear magnetic resonance (NMR) spectroscopy. To promote environmental-friendliness, biodegradable polycaprolactone (PCL) was chosen to supply the soft segment of polyurethane (PU), methylene diphenyl diisocyanate to supply the hard segment, The successful introduction of AMPF into the PCL-based PU enabled the production of AMPF/PUs. To investigate the effect of AMPF on PCL-based PU, NMR and gel permeation chromatography were performed for the preliminary analysis of AMPF/PUs; curve fitting was applied in Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. The atomic force microscopy to determine the difference in van der Waals forces and microphase separation in AMPF/PUs; a thermal gravimetric analysis and dynamic mechanical analysis were conducted to determine the thermal properties of AMPF/PUs, and tensile test were conducted to determine the mechanical properties of AMPF/PUs. The results reveal that AMPF/PUs have a high degree of microphase separation, and the heat resistance of AMPF/PUs can be improved by 4–5 %, while the tensile strength can be increased by about 28 MPa with the increase of AMPF content. From the contact angle test, it is known that the increase of AMPF content can convert the hydrophilic polyurethane (77.8 ± 2.7°) into the hydrophobic (95.2 ± 2.1°) polyurethane. Therefore, it is shown that AMPF can not only improve the strength of polyurethane but also provide hydrophobic properties. This fluorinated chain extender shows considerable potential for the coatings materials and waterproof and breathable fabrics.</description><subject>19F-19F NMR</subject><subject>Atomic beam spectroscopy</subject><subject>Atomic force microscopy</subject><subject>Biodegradability</subject><subject>Chains</subject><subject>Contact angle</subject><subject>Curve fitting</subject><subject>Diisocyanates</subject><subject>Dynamic mechanical analysis</subject><subject>Fluorinated</subject><subject>Fluorination</subject><subject>Gravimetric analysis</subject><subject>Heat resistance</subject><subject>Hydrophobicity</subject><subject>Liquid chromatography</subject><subject>MDI derived polyurethane</subject><subject>Mechanical properties</subject><subject>Microphase separation</subject><subject>NMR</subject><subject>NMR spectroscopy</subject><subject>Nuclear magnetic resonance</subject><subject>Photoelectrons</subject><subject>Polycaprolactone</subject><subject>Polyurethane</subject><subject>Polyurethane resins</subject><subject>Separation</subject><subject>Spectrum analysis</subject><subject>Synthesis</subject><subject>Tensile strength</subject><subject>Tensile tests</subject><subject>Thermal resistance</subject><subject>Thermodynamic properties</subject><subject>Van der Waals forces</subject><issn>0300-9440</issn><issn>1873-331X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkM1KAzEURoMoWKuvIAOup95MMtNmpxT_oOBCBXchzdy0KW0yJplC397U0bWrQPKdL_ceQq4pTCjQ5nYz6XxYaa_SpILqeFlPoTohIzqbspIx-nlKRsAASsE5nJOLGDcA0DAmRiS-HVxaY7SxUK4tuuA7DMliLLwpom2x0GtlXWG2vQ_WqYQ55LeHPmBaK4cDhnu17VWy3h2xTLhVfsnYzurcuFYRi4idCj-ZS3Jm1Dbi1e85Jh-PD-_z53Lx-vQyv1-UmnFIpQGBYGYUtFrWihtaG0Te1HWzBENh2QrWGCqYnrZLYFy0tKaNYLyqGM64mLExuRl681ZfPcYkN74PLn8pq2yCC1pznlPNkMqTxhjQyC7YnQoHSUEeBcuN_BMsj4LlIDiDdwOIeYe9xSCjtug0tjagTrL19r-Kb1Q7iZ0</recordid><startdate>202008</startdate><enddate>202008</enddate><creator>Li, Jia-Wun</creator><creator>Tsai, Hui-An</creator><creator>Lee, Hsun-Tsing</creator><creator>Cheng, Yung-Hsin</creator><creator>Chiu, Chih-Wei</creator><creator>Suen, Maw-Cherng</creator><general>Elsevier B.V</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>202008</creationdate><title>Synthesis and properties of side chain fluorinated polyurethanes and evaluation of changes in microphase separation</title><author>Li, Jia-Wun ; Tsai, Hui-An ; Lee, Hsun-Tsing ; Cheng, Yung-Hsin ; Chiu, Chih-Wei ; Suen, Maw-Cherng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-f09e0f810cab5a4f15fee46556b0f10bd936f193c7db0349d1516934223e84983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>19F-19F NMR</topic><topic>Atomic beam spectroscopy</topic><topic>Atomic force microscopy</topic><topic>Biodegradability</topic><topic>Chains</topic><topic>Contact angle</topic><topic>Curve fitting</topic><topic>Diisocyanates</topic><topic>Dynamic mechanical analysis</topic><topic>Fluorinated</topic><topic>Fluorination</topic><topic>Gravimetric analysis</topic><topic>Heat resistance</topic><topic>Hydrophobicity</topic><topic>Liquid chromatography</topic><topic>MDI derived polyurethane</topic><topic>Mechanical properties</topic><topic>Microphase separation</topic><topic>NMR</topic><topic>NMR spectroscopy</topic><topic>Nuclear magnetic resonance</topic><topic>Photoelectrons</topic><topic>Polycaprolactone</topic><topic>Polyurethane</topic><topic>Polyurethane resins</topic><topic>Separation</topic><topic>Spectrum analysis</topic><topic>Synthesis</topic><topic>Tensile strength</topic><topic>Tensile tests</topic><topic>Thermal resistance</topic><topic>Thermodynamic properties</topic><topic>Van der Waals forces</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Jia-Wun</creatorcontrib><creatorcontrib>Tsai, Hui-An</creatorcontrib><creatorcontrib>Lee, Hsun-Tsing</creatorcontrib><creatorcontrib>Cheng, Yung-Hsin</creatorcontrib><creatorcontrib>Chiu, Chih-Wei</creatorcontrib><creatorcontrib>Suen, Maw-Cherng</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Progress in organic coatings</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Jia-Wun</au><au>Tsai, Hui-An</au><au>Lee, Hsun-Tsing</au><au>Cheng, Yung-Hsin</au><au>Chiu, Chih-Wei</au><au>Suen, Maw-Cherng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and properties of side chain fluorinated polyurethanes and evaluation of changes in microphase separation</atitle><jtitle>Progress in organic coatings</jtitle><date>2020-08</date><risdate>2020</risdate><volume>145</volume><spage>105702</spage><pages>105702-</pages><artnum>105702</artnum><issn>0300-9440</issn><eissn>1873-331X</eissn><abstract>•This study successfully prepared a side chain fluorinated chain extender and introduced into polyurethane.•19F NMR, 19F-19F NMR successfully resolved and determined the structure of fluorinated chain extender.•Calculate the degree of microphase separation of AMPF/PUs by FTIR curve fitting.•Side chain fluorinated chain extender can effectively improve the mechanical properties of polyurethane.
To develop marketable new waterproof and breathable membranes, this study successfully applied a simple synthesis method to combine pentadecafluorooctanoyl chloride and 2-Amino-2-methyl-1,3-propanediol into a novel long-segment side-chain fluorinated chain extender (AMPF), the structure was examined using nuclear magnetic resonance (NMR) spectroscopy. To promote environmental-friendliness, biodegradable polycaprolactone (PCL) was chosen to supply the soft segment of polyurethane (PU), methylene diphenyl diisocyanate to supply the hard segment, The successful introduction of AMPF into the PCL-based PU enabled the production of AMPF/PUs. To investigate the effect of AMPF on PCL-based PU, NMR and gel permeation chromatography were performed for the preliminary analysis of AMPF/PUs; curve fitting was applied in Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. The atomic force microscopy to determine the difference in van der Waals forces and microphase separation in AMPF/PUs; a thermal gravimetric analysis and dynamic mechanical analysis were conducted to determine the thermal properties of AMPF/PUs, and tensile test were conducted to determine the mechanical properties of AMPF/PUs. The results reveal that AMPF/PUs have a high degree of microphase separation, and the heat resistance of AMPF/PUs can be improved by 4–5 %, while the tensile strength can be increased by about 28 MPa with the increase of AMPF content. From the contact angle test, it is known that the increase of AMPF content can convert the hydrophilic polyurethane (77.8 ± 2.7°) into the hydrophobic (95.2 ± 2.1°) polyurethane. Therefore, it is shown that AMPF can not only improve the strength of polyurethane but also provide hydrophobic properties. This fluorinated chain extender shows considerable potential for the coatings materials and waterproof and breathable fabrics.</abstract><cop>Lausanne</cop><pub>Elsevier B.V</pub><doi>10.1016/j.porgcoat.2020.105702</doi></addata></record> |
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subjects | 19F-19F NMR Atomic beam spectroscopy Atomic force microscopy Biodegradability Chains Contact angle Curve fitting Diisocyanates Dynamic mechanical analysis Fluorinated Fluorination Gravimetric analysis Heat resistance Hydrophobicity Liquid chromatography MDI derived polyurethane Mechanical properties Microphase separation NMR NMR spectroscopy Nuclear magnetic resonance Photoelectrons Polycaprolactone Polyurethane Polyurethane resins Separation Spectrum analysis Synthesis Tensile strength Tensile tests Thermal resistance Thermodynamic properties Van der Waals forces |
title | Synthesis and properties of side chain fluorinated polyurethanes and evaluation of changes in microphase separation |
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