Carbon Nanotube Migration in a Compatibilized Blend System, Leading to Kinetically Induced Enhancement in Electrical Conductivity and Mechanical Properties
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作者:
Azubuike, Lilian
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Univ Calgary, Dept Chem & Petr Engn, 2500 Univ Dr NW, Calgary, AB T2N 1N4, CanadaUniv Calgary, Dept Chem & Petr Engn, 2500 Univ Dr NW, Calgary, AB T2N 1N4, Canada
Azubuike, Lilian
[1
]
Wang, Jun
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Hong Kong Univ Sci & Technol Guangzhou, Adv Mat Thrust, Guangzhou 511453, Peoples R China
Hong Kong Univ Sci & Technol, Dept Chem & Biol Engn, Hong Kong 999077, Peoples R ChinaUniv Calgary, Dept Chem & Petr Engn, 2500 Univ Dr NW, Calgary, AB T2N 1N4, Canada
Wang, Jun
[2
,3
]
Sundararaj, Uttandaraman
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Univ Calgary, Dept Chem & Petr Engn, 2500 Univ Dr NW, Calgary, AB T2N 1N4, CanadaUniv Calgary, Dept Chem & Petr Engn, 2500 Univ Dr NW, Calgary, AB T2N 1N4, Canada
Sundararaj, Uttandaraman
[1
]
机构:
[1] Univ Calgary, Dept Chem & Petr Engn, 2500 Univ Dr NW, Calgary, AB T2N 1N4, Canada
[2] Hong Kong Univ Sci & Technol Guangzhou, Adv Mat Thrust, Guangzhou 511453, Peoples R China
[3] Hong Kong Univ Sci & Technol, Dept Chem & Biol Engn, Hong Kong 999077, Peoples R China
Kinetic factors that facilitate carbon nanotube (CNT) migration in a polymer blend from a high-density polyethylene (HDPE) phase to a poly (p-phenylene ether) (PPE) phase were studied, with the objective to induce CNT migration and localization at the interface. Herein, a CNT filler was pre-localized in an HDPE polymer and then blended with PPE at different blend compositions of 20:80, 40:60, 60:40, and 80:20 of PPE/HDPE at a constant filler concentration of 1 wt%. The level of CNT migration was studied at different mixing times of 5 and 10 min. The electrical conductivity initially increased by 2-3 orders of magnitude, with an increase in the PPE content up to 40%, and then it decreased significantly by up to 12 orders of magnitude at high PPE content up to 100%. We determined that the extent of migration was related to the difference in the melt viscosity between the constituent polymers. A triblock copolymer styrene-ethylene/butylene-styrene (SEBS) was used to improve the blend miscibility, and 2 wt% copolymer was found to be the optimum concentration for the electrical properties for the two blend compositions of 20:80 and 80:20 of PPE/HDPE, at a constant filler concentration of 1 wt%. The introduction of the SEBS triblock copolymer significantly increased the conductivity almost by almost four orders of magnitude for PPE/HDPE/80:20 composites with 1 wt% CNT and 2 wt% SEBS compared to the uncompatibilized blend nanocomposite. The mechanical strength of the compatibilized blend nanocomposites was found to be higher than the unfilled compatibilized blend (i.e., without CNT), uncompatibilized blend nanocomposites, and the pristine blend, illustrating the synergistic effect of adding nanofillers and a compatibilizer. SEM and TEM microstructures were used to interpret the structure-property relationships of these polymer blend nanocomposites.
机构:
Indian Inst Technol, Dept Met Engn & Mat Sci, Bombay 400076, Maharashtra, IndiaIndian Inst Technol, Dept Met Engn & Mat Sci, Bombay 400076, Maharashtra, India
Bose, Suryasarathi
;
Bhattacharyya, Arup R.
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Indian Inst Technol, Dept Met Engn & Mat Sci, Bombay 400076, Maharashtra, IndiaIndian Inst Technol, Dept Met Engn & Mat Sci, Bombay 400076, Maharashtra, India
Bhattacharyya, Arup R.
;
Kulkarni, Ajit R.
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Indian Inst Technol, Dept Met Engn & Mat Sci, Bombay 400076, Maharashtra, IndiaIndian Inst Technol, Dept Met Engn & Mat Sci, Bombay 400076, Maharashtra, India
Kulkarni, Ajit R.
;
Poetschke, Petra
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机构:
Leibniz Inst Polymer Res Dresden, Dept Polymer React & Blends, D-01069 Dresden, GermanyIndian Inst Technol, Dept Met Engn & Mat Sci, Bombay 400076, Maharashtra, India
机构:
Helmholtz Zentrum Geesthacht, Polymer Res Inst, D-21502 Geesthacht, GermanyHelmholtz Zentrum Geesthacht, Polymer Res Inst, D-21502 Geesthacht, Germany
Du, Bing
;
Handge, Ulrich A.
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Helmholtz Zentrum Geesthacht, Polymer Res Inst, D-21502 Geesthacht, GermanyHelmholtz Zentrum Geesthacht, Polymer Res Inst, D-21502 Geesthacht, Germany
Handge, Ulrich A.
;
Majeed, Shahid
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Helmholtz Zentrum Geesthacht, Polymer Res Inst, D-21502 Geesthacht, GermanyHelmholtz Zentrum Geesthacht, Polymer Res Inst, D-21502 Geesthacht, Germany
Majeed, Shahid
;
Abetz, Volker
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Helmholtz Zentrum Geesthacht, Polymer Res Inst, D-21502 Geesthacht, GermanyHelmholtz Zentrum Geesthacht, Polymer Res Inst, D-21502 Geesthacht, Germany
机构:
Indian Inst Technol, Dept Met Engn & Mat Sci, Bombay 400076, Maharashtra, IndiaIndian Inst Technol, Dept Met Engn & Mat Sci, Bombay 400076, Maharashtra, India
Bose, Suryasarathi
;
Bhattacharyya, Arup R.
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机构:
Indian Inst Technol, Dept Met Engn & Mat Sci, Bombay 400076, Maharashtra, IndiaIndian Inst Technol, Dept Met Engn & Mat Sci, Bombay 400076, Maharashtra, India
Bhattacharyya, Arup R.
;
Kulkarni, Ajit R.
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机构:
Indian Inst Technol, Dept Met Engn & Mat Sci, Bombay 400076, Maharashtra, IndiaIndian Inst Technol, Dept Met Engn & Mat Sci, Bombay 400076, Maharashtra, India
Kulkarni, Ajit R.
;
Poetschke, Petra
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机构:
Leibniz Inst Polymer Res Dresden, Dept Polymer React & Blends, D-01069 Dresden, GermanyIndian Inst Technol, Dept Met Engn & Mat Sci, Bombay 400076, Maharashtra, India
机构:
Helmholtz Zentrum Geesthacht, Polymer Res Inst, D-21502 Geesthacht, GermanyHelmholtz Zentrum Geesthacht, Polymer Res Inst, D-21502 Geesthacht, Germany
Du, Bing
;
Handge, Ulrich A.
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Helmholtz Zentrum Geesthacht, Polymer Res Inst, D-21502 Geesthacht, GermanyHelmholtz Zentrum Geesthacht, Polymer Res Inst, D-21502 Geesthacht, Germany
Handge, Ulrich A.
;
Majeed, Shahid
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Helmholtz Zentrum Geesthacht, Polymer Res Inst, D-21502 Geesthacht, GermanyHelmholtz Zentrum Geesthacht, Polymer Res Inst, D-21502 Geesthacht, Germany
Majeed, Shahid
;
Abetz, Volker
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Helmholtz Zentrum Geesthacht, Polymer Res Inst, D-21502 Geesthacht, GermanyHelmholtz Zentrum Geesthacht, Polymer Res Inst, D-21502 Geesthacht, Germany