TY - JOUR
T1 - In situ covalent bonding in polymerization to construct robust hydrogel lubrication coating on surface of silicone elastomer
AU - Gao, Luyao
AU - Ma, Shuanhong
AU - Ma, Zhengfeng
AU - Zheng, Zijian
AU - Zhou, Feng
AU - Liang, Yongmin
N1 - Funding Information:
We gratefully acknowledge support from the National Key Research and Development Program of China ( 2016YFC1100401 ), the National Natural Science Foundation of China ( 51705507 , 51805514 , 51828302 ). Professor Zhou thanks to the project of Bureau of International Cooperation, Chinese Academy of Sciences ( 121B62KYSB2017009 ) and CAS ( QYZDY-SSWJSC013 ).
Funding Information:
We gratefully acknowledge support from the National Key Research and Development Program of China (2016YFC1100401), the National Natural Science Foundation of China (51705507, 51805514, 51828302). Professor Zhou thanks to the project of Bureau of International Cooperation, Chinese Academy of Sciences (121B62KYSB2017009) and CAS (QYZDY-SSWJSC013).
Publisher Copyright:
© 2020 Elsevier B.V.
PY - 2020/8/20
Y1 - 2020/8/20
N2 - With the great process of hydrogels-based lubricating materials, it is still a big challenge to controllably and firmly modify thin hydrogels lubrication film onto the surface of elastic/hydrophobic substrates with low surface energy. Herein, one novel strategy to grow firm hydrogels lubrication coating on the surface of PDMS elastomer is reported by the combination of surface catalytic initiated radical polymerization (SCIRP) method and in situ bridge molecule anchoring strategy. In typical case, PAAm/PAA hydrogels lubrication layer can be in situ generated and covalently anchored on the surface of PDMS by using –C=C groups as coupling sites in the assembled KH570 molecule at ambient temperature. Meanwhile, the thickness of the growth hydrogels layer is highly controllable and can be finely regulated from dozens of micrometers to several hundred micrometers. The bonding strength of the growth hydrogels layer against PDMS substrate can be achieved to 30 N/m. Correspondingly, the growth hydrogels layer demonstrates excellent water-lubrication and anti-wear properties based on these above characteristics. We believe that this method would exhibit potential applications in the fields of biomedical device, microfluidic and soft actuation.
AB - With the great process of hydrogels-based lubricating materials, it is still a big challenge to controllably and firmly modify thin hydrogels lubrication film onto the surface of elastic/hydrophobic substrates with low surface energy. Herein, one novel strategy to grow firm hydrogels lubrication coating on the surface of PDMS elastomer is reported by the combination of surface catalytic initiated radical polymerization (SCIRP) method and in situ bridge molecule anchoring strategy. In typical case, PAAm/PAA hydrogels lubrication layer can be in situ generated and covalently anchored on the surface of PDMS by using –C=C groups as coupling sites in the assembled KH570 molecule at ambient temperature. Meanwhile, the thickness of the growth hydrogels layer is highly controllable and can be finely regulated from dozens of micrometers to several hundred micrometers. The bonding strength of the growth hydrogels layer against PDMS substrate can be achieved to 30 N/m. Correspondingly, the growth hydrogels layer demonstrates excellent water-lubrication and anti-wear properties based on these above characteristics. We believe that this method would exhibit potential applications in the fields of biomedical device, microfluidic and soft actuation.
KW - Hydrogels coating
KW - Interface bonding
KW - Surface polymerization
KW - Water lubrication
KW - Wear-resistance
UR - http://www.scopus.com/inward/record.url?scp=85084186420&partnerID=8YFLogxK
U2 - 10.1016/j.colsurfa.2020.124753
DO - 10.1016/j.colsurfa.2020.124753
M3 - Journal article
AN - SCOPUS:85084186420
SN - 0927-7757
VL - 599
JO - Colloids and Surfaces A: Physicochemical and Engineering Aspects
JF - Colloids and Surfaces A: Physicochemical and Engineering Aspects
M1 - 124753
ER -