Electrochemical membrane filtration is widely reported
to enhance
water contaminants’ degradation or rejection via anodic oxidation
or cathodic repulsion. Despite their advances, electrochemical membranes
or electrocatalysts often suffer from corrosion or passivation, especially
under strong electrode potentials or reactions. Moreover, the formation
of toxic byproducts, such as chlorinated organic compounds and oxyhalides
(e.g., ClO4
–) is another major concern.
This study investigated the membrane aging processes of two types
of conductive membranes, multiwalled carbon nanotubes (MWCNTs) and
ferrite/graphitic carbon nitride hybrids (Fe3O4@g-C3N4) coated on ceramic membranes. Under
high current densities (∼20 mA·cm–2)
with anodic potentials (∼10 V), MWCNTs and Fe3O4@g-C3N4 catalysts underwent evident
oxidation as indicated by an increase of the intensity ratio of the
Raman spectral bands (I
D/I
G) and charge transfer resistance (R
ct) of two electrochemical membranes. Under variations of electrode
potentials, chloride or bromide were shown to be oxidized to bromate
(BrO3
–) and chlorate (ClO3
–) at levels of 1–10 mmol·L–1. The formation of BrO3
– and ClO3
– was dependent on the solution pH, current
densities (1–20 mA·cm–2), and initial
concentrations of Br or Cl ions. To warrant a safe and rational design
and operation of electrochemically reactive membrane processes, membrane
aging and toxic byproduct’s formation deserve careful characterization
under relevant water filtration environments.