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High-cycle-life and high-loading copolymer network with potential application as a soft actuator

Rehman, Hafeez Ur (författare)
Shanghai Jiao Tong Univ, Sch Mat Sci & Engn, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China.
Chen, Yujie (författare)
Shanghai Jiao Tong Univ, Sch Mat Sci & Engn, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China.
Hedenqvist, Mikael S. (författare)
KTH,Fiber- och polymerteknologi
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Pathan, Radan (författare)
Shanghai Jiao Tong Univ, Dept Automat, Shanghai 200240, Peoples R China.
Liu, Hezhou (författare)
Shanghai Jiao Tong Univ, Collaborat Innovat Ctr Adv Ship & Dee Sea Explora, Shanghai 200240, Peoples R China.
Wang, Hesheng (författare)
Shanghai Jiao Tong Univ, Dept Automat, Shanghai 200240, Peoples R China.
Chen, Tao (författare)
Shanghai Jiao Tong Univ, Sch Mat Sci & Engn, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China.
Zhang, Xiaomiao (författare)
Shanghai Gen Hosp, Songjiang Rd 650, Shanghai 201620, Peoples R China.
Li, Hua (författare)
Shanghai Jiao Tong Univ, Collaborat Innovat Ctr Adv Ship & Dee Sea Explora, Shanghai 200240, Peoples R China.
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Shanghai Jiao Tong Univ, Sch Mat Sci & Engn, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China Fiber- och polymerteknologi (creator_code:org_t)
ELSEVIER SCI LTD, 2019
2019
Engelska.
Ingår i: Materials & design. - : ELSEVIER SCI LTD. - 0264-1275 .- 1873-4197. ; 182
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Thermo-responsive polymer materials ate appealing in emerging fields including soft robotics, artificial muscles, and actuators. However, realising a single smart polymer material that can achieve immense strain, fast actuation, and high loading remains a challenge. We attempted to address these limitations by fabricating a thermo-responsive copolymer network structure of poly(urethane-caprolactone-siloxane). The relative concentrations of these precursors were adjusted to realise a high mechanical strength of >= 17 MPa, 100% shape fixation, and a quick shape recovery time of <= 15 s. Experimental results revealed that the soft segments largely determines the extensibility and crystallinity of the copolymer material. The thermal gradient of the soft part enables the copolymer to self-heal during shape recovery. The copolymer network was applied to a load lifting device as an artificial muscle and was able to lift 200 times its weight with a short response time of <5 s and maximum power density that was half that of mammalian skeletal muscles. With its fast actuation, high loading, and self-healing abilities, the developed therrno-activated smart copolymer material is potentially applicable to a wide range of fields such as soft robotics, biomimetic devices, and prosthetics.

Ämnesord

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)

Nyckelord

Shape memory
Self-healing
Artificial muscle
Polyurethane
Polydimethylsiloxane
Kemi
Chemistry
Kemi
Chemistry

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