Cellulose-based membranes
have tremendous potential to
improve
the sustainability and performance of high value applications, such
as filters and energy devices, particularly as fluorinated compounds
are becoming more regulated. Yet, a deeper understanding of how cellulose
films are formed and their structure, in both the wet and dry state,
is needed to meet application specific demands and scale-up. We investigated
cellulose dewatering using dead-end filtration and the effect of particle
size, pressure, temperature, ionic strength, and pH were explored.
Dewatering times, filtration cake resistance and compressibility of
microfibrillated celluloses (MFCs) and cellulose nanofibrils (CNFs),
(and a combination thereof) were measured to understand the role of
fibrillation and intermolecular forces during dewatering and forming
of membranes. In this fundamental work, dewatering behavior was well
described by conventional filtration theory and increasing the pressure
from 1 to 4 bar reduced dewatering times by one-half with no significant
impact on the mechanical properties. Cake compressibility was found
to be directly related to particle size and degree of fibrillation,
indicating that finer grades of MFCs and CNFs could be more effectively
dewatered at higher pressures. Adjusting pH and ionic strength of
cellulose dispersions could similarly reduce dewatering times, yet
impacted the wet and dry mechanical properties. This work serves as
a basis to better understand the structure–property relationships
that develop during dewatering of MFCs and CNFs.