Electrochemical activity of sulfur networks synthesized through RAFT polymerization
C Almeida, H Costa, P Kadhirvel… - Journal of Applied …, 2016 - Wiley Online Library
Novel results concerning the inverse vulcanization of sulfur using reversible addition–
fragmentation chain transfer (RAFT) polymerization are here reported. It is shown that RAFT
polymerization can be used to carry out this crosslinking process, with the additional
possibility to extend the reaction time from a few minutes as with classical free radical
polymerization (FRP) to several hours. Higher control on viscosity and processability of the
synthesized networks, as well as, the implementation of semibatch feed policies during …
fragmentation chain transfer (RAFT) polymerization are here reported. It is shown that RAFT
polymerization can be used to carry out this crosslinking process, with the additional
possibility to extend the reaction time from a few minutes as with classical free radical
polymerization (FRP) to several hours. Higher control on viscosity and processability of the
synthesized networks, as well as, the implementation of semibatch feed policies during …
Electrochemical activity of sulfur networks synthesized through RAFT polymerization
M Costa, C Almeida, H Costa, AM Queiroz, RCS Dias… - 2016 - repositorio-aberto.up.pt
Novel results concerning the inverse vulcanization of sulfur using reversible addition-
fragmentation chain transfer (RAFT) polymerization are here reported. It is shown that RAFT
polymerization can be used to carry out this crosslinking process, with the additional
possibility to extend the reaction time from a few minutes as with classical free radical
polymerization (FRP) to several hours. Higher control on viscosity and processability of the
synthesized networks, as well as, the implementation of semibatch feed policies during …
fragmentation chain transfer (RAFT) polymerization are here reported. It is shown that RAFT
polymerization can be used to carry out this crosslinking process, with the additional
possibility to extend the reaction time from a few minutes as with classical free radical
polymerization (FRP) to several hours. Higher control on viscosity and processability of the
synthesized networks, as well as, the implementation of semibatch feed policies during …