globalchange  > 过去全球变化的重建
DOI: 10.1002/pi.5803
WOS记录号: WOS:000467962300013
论文题名:
Toward superior applications of thermoplastic elastomer blends: double T-g increase and improved ductility
作者: Burgoa, Aizeti1; Hernandez, Ricardo1; Vilas, Jose L.2,3
通讯作者: Burgoa, Aizeti
刊名: POLYMER INTERNATIONAL
ISSN: 0959-8103
EISSN: 1097-0126
出版年: 2019
卷: 68, 期:6, 页码:1130-1139
语种: 英语
英文关键词: thermoplastic elastomer blend ; TPE ; glass transition temperature ; improved ductility ; interfacial interactions ; morphology
WOS关键词: GLASS-TRANSITION TEMPERATURE ; CO-CONTINUOUS STRUCTURES ; POLYMER BLENDS ; MECHANICAL-PROPERTIES ; NITRILE RUBBER ; REACTIVE COMPATIBILISATION ; MORPHOLOGY DEVELOPMENT ; HEAT-RESISTANT ; MISCIBILITY ; BEHAVIOR
WOS学科分类: Polymer Science
WOS研究方向: Polymer Science
英文摘要:

With the aim of curbing air pollution and addressing climate change, the use of low density thermoplastic elastomers (TPEs) in transportation could be a useful way to lighten the vehicle weight. For that, melt blending of high performance rubber and thermoplastics is an attractive way of preparing high performance TPEs. In this work, several TPEs have been prepared by melt blending of hydrogenated acrylonitrile butadiene rubber (HNBR) with polyamide 6 (PA6), adding different amounts of carboxylated HNBR (XHNBR) as compatibilizer: 40/60/0, 40/42/18, 40/30/30 and 40/18/42 (PA6/HNBR/XHNBR). The resulting blends were investigated using melt rheological measurements, morphological observations (scanning electron microscopy and polarized optical microscopy), dynamic mechanical analysis, differential scanning calorimetry analysis and mechanical tests. A biphasic morphology was noted for all TPEs. An increase in XHNBR amount changes the morphology from dispersed to co-continuous. This evolution is explained by the change in the melt rheological properties of the HNBR/XHNBR rubber phase. Moreover, the introduction of 42% XHNBR resulted in an increase in the glass transition temperature of both rubber and PA6 phases. This double T-g increase phenomenon was attributed to the interfacial interactions between the carboxyl groups in XHNBR and the amine end groups in PA6. Additionally, thermal analysis revealed a reduced crystallinity of PA6 in the blend, which corresponds to enhanced interfacial interactions. The interfacial adhesion and the co-continuous morphology resulted in an improved ductility. This study reveals the possibility of obtaining TPE blends with tunable thermal and mechanical properties by controlling both interfacial interactions and morphology. (c) 2019 Society of Chemical Industry


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资源类型: 期刊论文
标识符: http://119.78.100.158/handle/2HF3EXSE/139731
Appears in Collections:过去全球变化的重建

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作者单位: 1.Leartiker S Coop, Polymer Dept, Markina Xemein, Spain
2.Univ Basque Country UPV EHU, Fac Sci & Technol, Dept Phys Chem, Macromol Chem Res Grp,Labquimac, Leioa, Spain
3.Basque Ctr Mat Applicat & Nanostruct, BCMat, UPV EHU Sci Pk, Leioa, Spain

Recommended Citation:
Burgoa, Aizeti,Hernandez, Ricardo,Vilas, Jose L.. Toward superior applications of thermoplastic elastomer blends: double T-g increase and improved ductility[J]. POLYMER INTERNATIONAL,2019-01-01,68(6):1130-1139
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