In
this present investigation, we applied an eco-friendly bacterial
cellulose (BC) membrane along with a polyethylene (PE) separator as
a separator for lead-acid battery systems. The key factor of the research
is to lower the cost of the lead-acid battery by introducing the BC
membrane along with a thin PE separator. The specific surface areas
of the BC membrane and the PE separator were 46.72 and 35.89 m2 g–1, respectively, with high porosity,
which can enhance the electrolyte uptake and movement. The identified
pore sizes of the BC membrane and the PE separator are 13.67 and 56.18
nm, respectively. The closely arranged microfibrils in the BC membrane
with the smaller pore size can uptake a high amount of electrolyte,
and it can hold it for a long period with the hydrogen interactions.
In addition, the BC membrane and the PE separator exhibited higher
thermal stabilities. The water uptake property of the BC membrane
is 130% at 30 °C, which results in considerable electrolyte uptake.
The ion exchange capacity of AGM, PE separator, and BC membrane are
∼0.0, ∼ 0.0, and 0.127 meq/g, respectively. The higher
IEC is attributed to the presence of hydrophilic functional groups
in the BC membrane, which increase the ion transportation in the membrane.
The ion conductivity of the BC membrane is considerably higher than
those of the AGM and PE separator. The charge and discharge performances
of the AGM and BC-PE battery systems were analyzed using lead-acid
battery cells. The exhibited discharge performances of both battery
systems were considerably similar at 0.1 and 0.2 A discharge current.
The final discharge capacities of the AGM battery and the BC-PE battery
were 0.96 and 0.94 Ah, respectively, at 0.1 A under identical conditions.
A considerable cyclic stability was observed in the BC-PE battery
system during long-term operation. From our experimental analysis
results, a cost-effective hybrid combination of a BC membrane along
with a PE separator can be considered as an efficient separator for
lead-acid battery systems.