TY - JOUR
T1 - Soft silicone elastomers exhibiting large actuation strains
AU - Bele, Adrian
AU - Dascalu, Mihaela
AU - Tugui, Codrin
AU - Stiubianu, George Theodor
AU - Varganici, Cristian Dragos
AU - Racles, Carmen
AU - Cazacu, Maria
AU - Skov, Anne Ladegaard
N1 - Publisher Copyright:
© 2022 Wiley Periodicals LLC.
PY - 2022
Y1 - 2022
N2 - Poly(dimethyl-co-methylvinyl)siloxane-α,ω-diols with 1.5, 5.5, and 8.5 mol% vinyl group contents, respectively, are obtained via an environmental friendly synthesis and used as platforms for further chemical modification via a green process. This chemical modification consists of UV-activated thiol-ene addition of 3-chloro-1-propanethiol to the vinyl groups, as proven by NMR analysis. Cross-linking with tetraethyl orthosilicate (in excess) of such modified polymers leads to dielectric elastomers with higher values of dielectric permittivity than those of non-chemically modified vinyl copolymers cross-linked under similar conditions. In addition, at high chloropropyl content, there is a significant decrease in Young's modulus, attributed to the plasticizing effect of the alkyl segment of the attached chloropropyl, and only a slight increase in breakdown strength is observed. All these changes induced by the chloropropyl group act synergistically in favor of the electromechanical performances of the resulting elastomers that exhibit large out-of-plane actuation strains of 53% and 61% for polar contents of 5.5 and 8.5 mol%, respectively, at an applied electric field of 40 V/μm. These are to the best of our knowledge the largest out-of-plane actuation strains from silicone elastomers reported in literature.
AB - Poly(dimethyl-co-methylvinyl)siloxane-α,ω-diols with 1.5, 5.5, and 8.5 mol% vinyl group contents, respectively, are obtained via an environmental friendly synthesis and used as platforms for further chemical modification via a green process. This chemical modification consists of UV-activated thiol-ene addition of 3-chloro-1-propanethiol to the vinyl groups, as proven by NMR analysis. Cross-linking with tetraethyl orthosilicate (in excess) of such modified polymers leads to dielectric elastomers with higher values of dielectric permittivity than those of non-chemically modified vinyl copolymers cross-linked under similar conditions. In addition, at high chloropropyl content, there is a significant decrease in Young's modulus, attributed to the plasticizing effect of the alkyl segment of the attached chloropropyl, and only a slight increase in breakdown strength is observed. All these changes induced by the chloropropyl group act synergistically in favor of the electromechanical performances of the resulting elastomers that exhibit large out-of-plane actuation strains of 53% and 61% for polar contents of 5.5 and 8.5 mol%, respectively, at an applied electric field of 40 V/μm. These are to the best of our knowledge the largest out-of-plane actuation strains from silicone elastomers reported in literature.
KW - Artificial muscles
KW - Dielectric elastomer
KW - Lateral strain
KW - Silicone
KW - Thiol-ene addition
U2 - 10.1002/app.52261
DO - 10.1002/app.52261
M3 - Journal article
AN - SCOPUS:85124532477
SN - 0021-8995
VL - 139
JO - Journal of Applied Polymer Science
JF - Journal of Applied Polymer Science
IS - 33
M1 - 52261
ER -