Evolution of crosslinking structure in vulcanized natural rubber during thermal aging in the presence of a constant compressive stress
•Constant compressive stress promoted the fracture of polysulfide and disulfide bonds.•Reactive sulfur-containing side (RSS) groups were formed under compressive stress.•RSS groups could participate in re-crosslinking reactions in the presence of heat.•RSS groups increased the hysteresis loss of NR...
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Veröffentlicht in: | Polymer degradation and stability 2023-11, Vol.217, p.110513, Article 110513 |
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creator | Kong, Yiran Chen, Xiangfei Li, Zhouxian Li, Guangxian Huang, Yajiang |
description | •Constant compressive stress promoted the fracture of polysulfide and disulfide bonds.•Reactive sulfur-containing side (RSS) groups were formed under compressive stress.•RSS groups could participate in re-crosslinking reactions in the presence of heat.•RSS groups increased the hysteresis loss of NR under deformation.
The evolution process of the crosslinking structure in sulfur-cured natural rubber (NR) under the combined effect of compressive stress and temperature was investigated using a homemade constant-stress device. The aged NR samples were characterized by infrared spectroscopy, chemical probe method, differential scanning calorimetry, and mechanical analysis. The results revealed that compressive stress promoted the breakage of sulfur bonds (mainly low-energy ones) between NR chains, leading to a decline in crosslink density and an increase in mesh size. According to the Arrhenius equation, a compressive stress of 1.78 MPa reduced the apparent activation energy for the breakage of polysulfide bonds from 56.3 kJ/mol to 48.2 kJ/mol, resulting in a 14.4% decrease. The sulfur-containing side groups formed after the breakage of polysulfide bonds not only participated in post-crosslinking reactions after stress release but also increased the hysteresis loss of NR under large deformation. |
doi_str_mv | 10.1016/j.polymdegradstab.2023.110513 |
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The evolution process of the crosslinking structure in sulfur-cured natural rubber (NR) under the combined effect of compressive stress and temperature was investigated using a homemade constant-stress device. The aged NR samples were characterized by infrared spectroscopy, chemical probe method, differential scanning calorimetry, and mechanical analysis. The results revealed that compressive stress promoted the breakage of sulfur bonds (mainly low-energy ones) between NR chains, leading to a decline in crosslink density and an increase in mesh size. According to the Arrhenius equation, a compressive stress of 1.78 MPa reduced the apparent activation energy for the breakage of polysulfide bonds from 56.3 kJ/mol to 48.2 kJ/mol, resulting in a 14.4% decrease. The sulfur-containing side groups formed after the breakage of polysulfide bonds not only participated in post-crosslinking reactions after stress release but also increased the hysteresis loss of NR under large deformation.</description><identifier>ISSN: 0141-3910</identifier><identifier>DOI: 10.1016/j.polymdegradstab.2023.110513</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>activation energy ; Aging ; calorimetry ; Compression stress ; Crosslinked network ; crosslinking ; deformation ; degradation ; equations ; evolution ; hysteresis ; infrared spectroscopy ; Natural rubber ; polymers ; rubber ; sulfur ; temperature</subject><ispartof>Polymer degradation and stability, 2023-11, Vol.217, p.110513, Article 110513</ispartof><rights>2023 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c366t-976fe014f8581188500917f9c4c88b3df1b6de4f325079c10599cf26f0799ab63</citedby><cites>FETCH-LOGICAL-c366t-976fe014f8581188500917f9c4c88b3df1b6de4f325079c10599cf26f0799ab63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S014139102300263X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids></links><search><creatorcontrib>Kong, Yiran</creatorcontrib><creatorcontrib>Chen, Xiangfei</creatorcontrib><creatorcontrib>Li, Zhouxian</creatorcontrib><creatorcontrib>Li, Guangxian</creatorcontrib><creatorcontrib>Huang, Yajiang</creatorcontrib><title>Evolution of crosslinking structure in vulcanized natural rubber during thermal aging in the presence of a constant compressive stress</title><title>Polymer degradation and stability</title><description>•Constant compressive stress promoted the fracture of polysulfide and disulfide bonds.•Reactive sulfur-containing side (RSS) groups were formed under compressive stress.•RSS groups could participate in re-crosslinking reactions in the presence of heat.•RSS groups increased the hysteresis loss of NR under deformation.
The evolution process of the crosslinking structure in sulfur-cured natural rubber (NR) under the combined effect of compressive stress and temperature was investigated using a homemade constant-stress device. The aged NR samples were characterized by infrared spectroscopy, chemical probe method, differential scanning calorimetry, and mechanical analysis. The results revealed that compressive stress promoted the breakage of sulfur bonds (mainly low-energy ones) between NR chains, leading to a decline in crosslink density and an increase in mesh size. According to the Arrhenius equation, a compressive stress of 1.78 MPa reduced the apparent activation energy for the breakage of polysulfide bonds from 56.3 kJ/mol to 48.2 kJ/mol, resulting in a 14.4% decrease. The sulfur-containing side groups formed after the breakage of polysulfide bonds not only participated in post-crosslinking reactions after stress release but also increased the hysteresis loss of NR under large deformation.</description><subject>activation energy</subject><subject>Aging</subject><subject>calorimetry</subject><subject>Compression stress</subject><subject>Crosslinked network</subject><subject>crosslinking</subject><subject>deformation</subject><subject>degradation</subject><subject>equations</subject><subject>evolution</subject><subject>hysteresis</subject><subject>infrared spectroscopy</subject><subject>Natural rubber</subject><subject>polymers</subject><subject>rubber</subject><subject>sulfur</subject><subject>temperature</subject><issn>0141-3910</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqNUD1PwzAUzAASpfAfvCCxJNhxkiYDA6rKh1SJBWbLcZ6LS2IH26lUfgC_G5swMeHF7z3f3fNdklwRnBFMqpt9Npr-OHSws7xznrdZjnOaEYJLQk-SBSYFSWlD8Fly7tweh1OUZJF8bQ6mn7wyGhmJhDXO9Uq_K71DzttJ-MkCUhodpl5wrT6hQ5qHIe-RndoWLOomG9H-DewQpnwXu8AIAzRacKAFRG2OhNHhZ9qHYogvTh0gbgnVRXIqee_g8vdeJq_3m5f1Y7p9fnha321TQavKp82qkhCsyLqsCanrEuOGrGQjClHXLe0kaasOCknzEq8aEcw3jZB5JUPX8Laiy-R61h2t-ZjAeTYoJ6DvuQYzOUZJSauALYsAvZ2hP6FYkGy0auD2yAhmMXO2Z38yZzFzNmce-A8zH4KfgwLLnFAxjE5ZEJ51Rv1T6RuIlJmG</recordid><startdate>202311</startdate><enddate>202311</enddate><creator>Kong, Yiran</creator><creator>Chen, Xiangfei</creator><creator>Li, Zhouxian</creator><creator>Li, Guangxian</creator><creator>Huang, Yajiang</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>202311</creationdate><title>Evolution of crosslinking structure in vulcanized natural rubber during thermal aging in the presence of a constant compressive stress</title><author>Kong, Yiran ; Chen, Xiangfei ; Li, Zhouxian ; Li, Guangxian ; Huang, Yajiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c366t-976fe014f8581188500917f9c4c88b3df1b6de4f325079c10599cf26f0799ab63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>activation energy</topic><topic>Aging</topic><topic>calorimetry</topic><topic>Compression stress</topic><topic>Crosslinked network</topic><topic>crosslinking</topic><topic>deformation</topic><topic>degradation</topic><topic>equations</topic><topic>evolution</topic><topic>hysteresis</topic><topic>infrared spectroscopy</topic><topic>Natural rubber</topic><topic>polymers</topic><topic>rubber</topic><topic>sulfur</topic><topic>temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kong, Yiran</creatorcontrib><creatorcontrib>Chen, Xiangfei</creatorcontrib><creatorcontrib>Li, Zhouxian</creatorcontrib><creatorcontrib>Li, Guangxian</creatorcontrib><creatorcontrib>Huang, Yajiang</creatorcontrib><collection>CrossRef</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Polymer degradation and stability</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kong, Yiran</au><au>Chen, Xiangfei</au><au>Li, Zhouxian</au><au>Li, Guangxian</au><au>Huang, Yajiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evolution of crosslinking structure in vulcanized natural rubber during thermal aging in the presence of a constant compressive stress</atitle><jtitle>Polymer degradation and stability</jtitle><date>2023-11</date><risdate>2023</risdate><volume>217</volume><spage>110513</spage><pages>110513-</pages><artnum>110513</artnum><issn>0141-3910</issn><abstract>•Constant compressive stress promoted the fracture of polysulfide and disulfide bonds.•Reactive sulfur-containing side (RSS) groups were formed under compressive stress.•RSS groups could participate in re-crosslinking reactions in the presence of heat.•RSS groups increased the hysteresis loss of NR under deformation.
The evolution process of the crosslinking structure in sulfur-cured natural rubber (NR) under the combined effect of compressive stress and temperature was investigated using a homemade constant-stress device. The aged NR samples were characterized by infrared spectroscopy, chemical probe method, differential scanning calorimetry, and mechanical analysis. The results revealed that compressive stress promoted the breakage of sulfur bonds (mainly low-energy ones) between NR chains, leading to a decline in crosslink density and an increase in mesh size. According to the Arrhenius equation, a compressive stress of 1.78 MPa reduced the apparent activation energy for the breakage of polysulfide bonds from 56.3 kJ/mol to 48.2 kJ/mol, resulting in a 14.4% decrease. The sulfur-containing side groups formed after the breakage of polysulfide bonds not only participated in post-crosslinking reactions after stress release but also increased the hysteresis loss of NR under large deformation.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.polymdegradstab.2023.110513</doi></addata></record> |
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subjects | activation energy Aging calorimetry Compression stress Crosslinked network crosslinking deformation degradation equations evolution hysteresis infrared spectroscopy Natural rubber polymers rubber sulfur temperature |
title | Evolution of crosslinking structure in vulcanized natural rubber during thermal aging in the presence of a constant compressive stress |
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