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dc.title | Low temperature crystallization behavior of natural rubber by dynamic mechanical analysis | en |
dc.contributor.author | Yao, Minglong | |
dc.contributor.author | Wang, Zhepeng | |
dc.contributor.author | Robertson, Christopher G. | |
dc.relation.ispartof | Rubber Chemistry And Technology | |
dc.identifier.issn | 0035-9475 Scopus Sources, Sherpa/RoMEO, JCR | |
dc.identifier.issn | 1943-4804 Scopus Sources, Sherpa/RoMEO, JCR | |
dc.date.issued | 2024 | |
utb.relation.volume | 97 | |
utb.relation.issue | 4 | |
dc.citation.spage | 619 | |
dc.citation.epage | 630 | |
dc.type | article | |
dc.language.iso | en | |
dc.publisher | American Chemical Society | |
dc.identifier.doi | 10.5254/rct.24.00050 | |
dc.relation.uri | https://meridian.allenpress.com/rct/article-abstract/97/4/619/503588/LOW-TEMPERATURE-CRYSTALLIZATION-BEHAVIOR-OF?redirectedFrom=fulltext | |
dc.description.abstract | A fundamental study of low temperature crystallization of natural rubber (NR) gum polymer (raw elastomer) was conducted using dynamic mechanical analysis (DMA) in oscillatory shear rheology mode. Isothermal crystallization was followed using DMA for crystallization temperatures ranging from-15 to-35 degrees C, with the maximum rate of crystallization noted at-25 degrees C. After the isothermal crystallization (annealing) for times from 6 to 9 h, DMA heating scans revealed two melting transitions (a and b ) with locations that depended on the prior annealing temperature. The locations of these melting transitions were comparable with literature results for melting peaks by differential scanning calorimetry. At temperatures above these melting transitions, we identified two additional relaxations in the DMA heating trace that did not depend on the prior crystallization history. We also found evidence of the melt memory effect in polymer crystallization, which is discussed. During annealing at-25 degrees C, high cis-1,4 isoprene rubber (IR) showed considerably slower and lower extent of crystallization than NR, and crosslinked NR did not show noticeable crystallization within the 12-h experiment. | en |
utb.faculty | University Institute | |
dc.identifier.uri | http://hdl.handle.net/10563/1012360 | |
utb.identifier.wok | 001412905400012 | |
utb.source | J-wok | |
dc.date.accessioned | 2025-02-25T14:29:32Z | |
dc.date.available | 2025-02-25T14:29:32Z | |
dc.description.sponsorship | Center for Frontier Research and Technology of Zhongce Rubber Group Co., Ltd. | |
utb.ou | Centre of Polymer Systems | |
utb.contributor.internalauthor | Robertson, Christopher G. | |
utb.fulltext.sponsorship | This paper is dedicated in memory of C. Michael Roland, who contributed immensely to the field of rubber physics, strongly supported the journal Rubber Chemistry and Technology as editor and author, and was an important mentor and friend to author C. G. Robertson. The authors thank Jean-Marc Chenal from INSA de Lyon (France) for providing DSC data from his 2007 publication. The Center for Frontier Research and Technology of Zhongce Rubber Group Co., Ltd. supported this research, for which we are grateful. We appreciate technical insights shared by Yi Zhu and Dezheng Tan from Zhongce Rubber Group Co., Ltd. | |
utb.wos.affiliation | [Yao, Minglong; Wang, Zhepeng] Zhongce Rubber Grp Co Ltd, Ctr Frontier Res & Technol, Hangzhou 310008, Zhejiang, Peoples R China; [Robertson, G. Christopher] Tomas Bata Univ Inzlin, Univ Inst, Ctr Polymer Syst, Tr Tomase Bati 5678, Zlin 76001, Czech Republic; [Robertson, G. Christopher] Polymer Technol Serv LLC, Akron, OH 44333 USA | |
utb.fulltext.projects | - |
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