scholarly journals Polymer Electrolytes with Exclusively Cationic Conductivity

1988 ◽  
Vol 135 ◽  
Author(s):  
H. Liu ◽  
Y. Okamoto ◽  
T. Skotheim ◽  
Y. S. Pak ◽  
S. G. Greenbaum ◽  
...  

AbstractThe synthesis of exclusively cation conducting polymer electrolytes based on a nylon-l backbone, ethylene-oxide side chains, and attached dibutyl phenolate anions is described. The tendency for ion pair formation appears to be reduced as the conductivity of the sodium-containing compound reaches −2 × 10−6 S-cm−1 at 50°C. 23Na nuclear magnetic resonance measurements demonstrate: i) motional narrowing of the mobile Na+ resonance above the glass transition temperature; ii) mobile Na+ concentrations of ∼75% at 40°C; iii) insensitivity of the linewidth to applied hydrostatic pressure up to 2 kbar. Similaries between these findings, and those in “conventional” polymer-salt electrolytes are discussed.

2013 ◽  
Vol 46 (21) ◽  
pp. 8580-8588 ◽  
Author(s):  
Nicolaas A. Stolwijk ◽  
Christian Heddier ◽  
Manuel Reschke ◽  
Manfred Wiencierz ◽  
Joachim Bokeloh ◽  
...  

1999 ◽  
Vol 42 (4) ◽  
pp. 1055-1060 ◽  
Author(s):  
R. R. Ruan ◽  
Z. Long ◽  
K. Chang ◽  
P. L. Chen ◽  
I. A. Taub

Gels ◽  
2021 ◽  
Vol 7 (2) ◽  
pp. 45
Author(s):  
Guodong Deng ◽  
Timothy D. Schoch ◽  
Kevin A. Cavicchi

Ion-pair comonomers (IPCs) where both the anion and cation contain polymerizable functional groups offer a route to prepare polyampholyte, ion-containing polymers. Polymerizing vinyl functional groups by free-radical polymerization produces bridging ion-pairs that act as non-covalent crosslinks between backbone segments. In particular the homopolymerization of the IPC vinyl benzyl tri-n-octylphosphonium styrene sulfonate produces a stiff, glassy polymer with a glass transition temperature (Tg) of 191 °C, while copolymerization with a non-ionic acrylate produces microphase separates ionomers with ion-rich and ion-poor domains. This work investigates the tuning of the Tg of the polyelectrolyte or ion-rich domains of the ionomers by copolymerizing with vinyl benzyl tri-n-octylphosphonium p-toluene sulfonic acid. This chemically similar repeat unit with pendant rather than bridging ion-pairs lowers the Tg compared to the polyelectrolyte or ionomer containing only the IPC segments. Rheological measurements were used to characterize the thermomechanical behavior and Tg of different copolymers. The Tg variation in the polyelectrolyte vs. weight fraction IPC could be fit with either the Gordon–Taylor or Couchman–Karasz equation. Copolymerization of IPC with a chemically similar cationic monomer offers a viable route to systematically vary the Tg of the resulting polymers useful for tailoring the material properties in applications such as elastomers or shape memory polymers.


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