Preparation and dynamic properties of an anisotropic natural rubber film as viewed by electron spin resonance-spin probe method
Natural rubber (NR) films with the thickness of about 1 mm were prepared by removing the liquid phase from NR latex, which was previously irradiated. The primary radiation dose varied from 0 kGy (for unirradiated NR) to 200 kGy. Dry NR films were uniaxially stretched, and the degree of deformation,...
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Veröffentlicht in: | Polymer engineering and science 2013-11, Vol.53 (11), p.2284-2291 |
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creator | Valić, Srećko Bonato, Jasminka Andreis, Mladen Klepac, Damir Didović, Mirna Petković |
description | Natural rubber (NR) films with the thickness of about 1 mm were prepared by removing the liquid phase from NR latex, which was previously irradiated. The primary radiation dose varied from 0 kGy (for unirradiated NR) to 200 kGy. Dry NR films were uniaxially stretched, and the degree of deformation, defined as λ = l/l0 (l0 and l being the lengths of relaxed and uniaxially deformed sample, respectively), was varied from λ = 1.0 (relaxed state) to λ = 2.7. Samples were then irradiated with secondary dose, which was chosen to be 100 or 200 kGy. NR films were characterized by differential scanning calorimetry and electron spin resonance–spin probe method. In addition, samples were exposed to accelerated thermal aging, and changes in molecular dynamics and structure were obtained. It has been shown that the application of deformation during the cross‐linking leads to the restriction in segmental mobility for the lower secondary dose, whereas for the higher secondary dose, larger values of λ induce an opposite effect originating from the structural changes. Thermally aged samples show higher amount of the gel phase and consequently higher fraction of slow motional chain segments. POLYM. ENG. SCI., 53:2284–2291, 2013. © 2013 Society of Plastics Engineers |
doi_str_mv | 10.1002/pen.23534 |
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The primary radiation dose varied from 0 kGy (for unirradiated NR) to 200 kGy. Dry NR films were uniaxially stretched, and the degree of deformation, defined as λ = l/l0 (l0 and l being the lengths of relaxed and uniaxially deformed sample, respectively), was varied from λ = 1.0 (relaxed state) to λ = 2.7. Samples were then irradiated with secondary dose, which was chosen to be 100 or 200 kGy. NR films were characterized by differential scanning calorimetry and electron spin resonance–spin probe method. In addition, samples were exposed to accelerated thermal aging, and changes in molecular dynamics and structure were obtained. It has been shown that the application of deformation during the cross‐linking leads to the restriction in segmental mobility for the lower secondary dose, whereas for the higher secondary dose, larger values of λ induce an opposite effect originating from the structural changes. Thermally aged samples show higher amount of the gel phase and consequently higher fraction of slow motional chain segments. POLYM. ENG. SCI., 53:2284–2291, 2013. © 2013 Society of Plastics Engineers</description><identifier>ISSN: 0032-3888</identifier><identifier>EISSN: 1548-2634</identifier><identifier>DOI: 10.1002/pen.23534</identifier><identifier>CODEN: PYESAZ</identifier><language>eng</language><publisher>Hoboken, NJ: Blackwell Publishing Ltd</publisher><subject>Anisotropy ; Applied sciences ; Chemical processes ; Crosslinking ; Deformation ; Differential scanning calorimetry ; Electron spin ; Exact sciences and technology ; Irradiation ; Mobility ; Molecular dynamics ; Molecular structure ; Natural polymers ; Natural rubber ; Physicochemistry of polymers ; Radiation ; Rubber</subject><ispartof>Polymer engineering and science, 2013-11, Vol.53 (11), p.2284-2291</ispartof><rights>Copyright © 2013 Society of Plastics Engineers</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2013 Society of Plastics Engineers, Inc.</rights><rights>Copyright Blackwell Publishing Ltd. 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The primary radiation dose varied from 0 kGy (for unirradiated NR) to 200 kGy. Dry NR films were uniaxially stretched, and the degree of deformation, defined as λ = l/l0 (l0 and l being the lengths of relaxed and uniaxially deformed sample, respectively), was varied from λ = 1.0 (relaxed state) to λ = 2.7. Samples were then irradiated with secondary dose, which was chosen to be 100 or 200 kGy. NR films were characterized by differential scanning calorimetry and electron spin resonance–spin probe method. In addition, samples were exposed to accelerated thermal aging, and changes in molecular dynamics and structure were obtained. It has been shown that the application of deformation during the cross‐linking leads to the restriction in segmental mobility for the lower secondary dose, whereas for the higher secondary dose, larger values of λ induce an opposite effect originating from the structural changes. Thermally aged samples show higher amount of the gel phase and consequently higher fraction of slow motional chain segments. POLYM. ENG. SCI., 53:2284–2291, 2013. © 2013 Society of Plastics Engineers</description><subject>Anisotropy</subject><subject>Applied sciences</subject><subject>Chemical processes</subject><subject>Crosslinking</subject><subject>Deformation</subject><subject>Differential scanning calorimetry</subject><subject>Electron spin</subject><subject>Exact sciences and technology</subject><subject>Irradiation</subject><subject>Mobility</subject><subject>Molecular dynamics</subject><subject>Molecular structure</subject><subject>Natural polymers</subject><subject>Natural rubber</subject><subject>Physicochemistry of polymers</subject><subject>Radiation</subject><subject>Rubber</subject><issn>0032-3888</issn><issn>1548-2634</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>N95</sourceid><recordid>eNp1kl9v0zAUxSMEEmXwwDewhJBAIp0T2_nzOI2xTprGBAMeLce56TwSJ_gmjD7x1bldy7SiIluxE__OcXx8o-hlwucJ5-nhAH6eCiXko2iWKFnEaSbk42jGuUhjURTF0-gZ4g0nVqhyFv2-DDCYYEbXe2Z8zeqVN52zbAj9AGF0gKxvaIW6w36kr7TozTgF07IwVRUE1ri2YwbZTwe3ULNqxaAFS6xnODjPAmDvjbcQ372SdQWsg_G6r59HTxrTIrzYjgfRlw8nV8eL-Pzj6dnx0XlsVS5lLEUjpDWZAglFbuqiKQuelypTdcFlY6Gp8jpTRV7WyqoypQbC2kTUKiurkouD6M3Glzb_MQGOunNooW2Nh35CnaiUl5LLNCH01T_oTT8FT3-nE1lmmcz5Q2ppWtDON5SNsWtTfSRkIQTP0vW28R5qCR4ovt4DJQe7_HwPT60GupS9grc7AmJG-DUuzYSozz5_2mXfPWCrCZ0HpAe65fWIG8k-axt6xACNHoLrTFjphOt1sWkqNn1XbMS-3mZm0Jq2CXTbDu8FaV4mMpcZcYcb7pbOsfq_ob48ufjrvE3QIR3sXmHCd53lIlf628UpzVL5_utioa_EH3At73U</recordid><startdate>201311</startdate><enddate>201311</enddate><creator>Valić, Srećko</creator><creator>Bonato, Jasminka</creator><creator>Andreis, Mladen</creator><creator>Klepac, Damir</creator><creator>Didović, Mirna Petković</creator><general>Blackwell Publishing Ltd</general><general>Wiley</general><general>Society of Plastics Engineers, Inc</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>N95</scope><scope>XI7</scope><scope>ISR</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>201311</creationdate><title>Preparation and dynamic properties of an anisotropic natural rubber film as viewed by electron spin resonance-spin probe method</title><author>Valić, Srećko ; Bonato, Jasminka ; Andreis, Mladen ; Klepac, Damir ; Didović, Mirna Petković</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5744-43f34ca65e4e87ad8f98079565d804fcefb7d65879d5c592929e3cc13d569b903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Anisotropy</topic><topic>Applied sciences</topic><topic>Chemical processes</topic><topic>Crosslinking</topic><topic>Deformation</topic><topic>Differential scanning calorimetry</topic><topic>Electron spin</topic><topic>Exact sciences and technology</topic><topic>Irradiation</topic><topic>Mobility</topic><topic>Molecular dynamics</topic><topic>Molecular structure</topic><topic>Natural polymers</topic><topic>Natural rubber</topic><topic>Physicochemistry of polymers</topic><topic>Radiation</topic><topic>Rubber</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Valić, Srećko</creatorcontrib><creatorcontrib>Bonato, Jasminka</creatorcontrib><creatorcontrib>Andreis, Mladen</creatorcontrib><creatorcontrib>Klepac, Damir</creatorcontrib><creatorcontrib>Didović, Mirna Petković</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Gale Business: Insights</collection><collection>Business Insights: Essentials</collection><collection>Gale In Context: Science</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Polymer engineering and science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Valić, Srećko</au><au>Bonato, Jasminka</au><au>Andreis, Mladen</au><au>Klepac, Damir</au><au>Didović, Mirna Petković</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation and dynamic properties of an anisotropic natural rubber film as viewed by electron spin resonance-spin probe method</atitle><jtitle>Polymer engineering and science</jtitle><addtitle>Polym Eng Sci</addtitle><date>2013-11</date><risdate>2013</risdate><volume>53</volume><issue>11</issue><spage>2284</spage><epage>2291</epage><pages>2284-2291</pages><issn>0032-3888</issn><eissn>1548-2634</eissn><coden>PYESAZ</coden><abstract>Natural rubber (NR) films with the thickness of about 1 mm were prepared by removing the liquid phase from NR latex, which was previously irradiated. The primary radiation dose varied from 0 kGy (for unirradiated NR) to 200 kGy. Dry NR films were uniaxially stretched, and the degree of deformation, defined as λ = l/l0 (l0 and l being the lengths of relaxed and uniaxially deformed sample, respectively), was varied from λ = 1.0 (relaxed state) to λ = 2.7. Samples were then irradiated with secondary dose, which was chosen to be 100 or 200 kGy. NR films were characterized by differential scanning calorimetry and electron spin resonance–spin probe method. In addition, samples were exposed to accelerated thermal aging, and changes in molecular dynamics and structure were obtained. It has been shown that the application of deformation during the cross‐linking leads to the restriction in segmental mobility for the lower secondary dose, whereas for the higher secondary dose, larger values of λ induce an opposite effect originating from the structural changes. Thermally aged samples show higher amount of the gel phase and consequently higher fraction of slow motional chain segments. POLYM. ENG. SCI., 53:2284–2291, 2013. © 2013 Society of Plastics Engineers</abstract><cop>Hoboken, NJ</cop><pub>Blackwell Publishing Ltd</pub><doi>10.1002/pen.23534</doi><tpages>8</tpages></addata></record> |
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subjects | Anisotropy Applied sciences Chemical processes Crosslinking Deformation Differential scanning calorimetry Electron spin Exact sciences and technology Irradiation Mobility Molecular dynamics Molecular structure Natural polymers Natural rubber Physicochemistry of polymers Radiation Rubber |
title | Preparation and dynamic properties of an anisotropic natural rubber film as viewed by electron spin resonance-spin probe method |
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