Interaction Analysis between Gravity-Driven Ceramic Membrane and Smaller Organic Matter: Implications for Retention and Fouling Mechanism in Ultralow Pressure-Driven Filtration System.

Gravity-driven membranes (GDM) generally achieve high retention performance in filtration of organic matter with a smaller size than the membrane pore, yet the in-depth mechanism remains unclear. Thorough analysis of the retention mechanism is crucial for optimizing GDM properties and improving GDM filtration performance. The performance and interaction mechanism of gravity-driven ceramic membrane (GDCM) filtrating smaller organic matter (SOM) were systematically studied. Rejection rate grew noticeably for like-charged foulant, whereas it only grew slightly for opposite-charged foulant as operation height decreased. Flux declined more seriously at lower operation height, probably due to heavier cake fouling caused by the rejected foulant. Interactions of ceramic membrane-SOM were analyzed through extended Derjaguin-Landau-Verwey-Overbeek theory (XDLVO) and hydrodynamic permeation drag (PD). Among van der Waals (LW), acid-base (AB), and electrostatic (EL) forces in XDLVO, EL played a significant role on GDCM filtrating SOM, and altering membrane electrostatic property could greatly influence SOM filtration. Furthermore, the rising PD force largely weakened the EL dominant zone with operation height increasing, while barely influencing the LW and AB dominant zones. Therefore, the weakened EL-dominant repulsive zone caused less rejection of like-charged foulant with operation height increasing. Fe2O3- and MnO2-modified membranes further validated the comprehensive influence of LW, AB, EL, and PD interactions on GDCM filtration. The possible "trade-off" of pore blocking-cake fouling with operation height decreasing demonstrated potential enhancement for both rejection and antifouling performance by electrically modified membrane under ultralow pressure. This study provides insight on membrane selection/preparation/modification and performance control of ultralow pressure-driven filtration.

Synergistic oxidation - filtration process analysis of catalytic CuFe2O4 - Tailored ceramic membrane filtration via peroxymonosulfate activation for humic acid treatment.

This work synthesized catalytic CuFe2O4 tailored ceramic membrane (CuFeCM), and systematically investigated the intercorrelated oxidation - filtration mechanism of peroxymonosulfate (PMS)/CuFeCM catalytic filtration for treating humic acid (HA). PMS/CuFeCM filtration exhibited enhanced HA removal efficiency while reduced the irreversible fouling resistance as compared with the conventional CM filtration. Results from HA characterizations showed that PMS/CuFeCM catalytic filtration oxidized HA into conjugated structures of smaller molecular weight. The unsaturated bonds further caused the re-agglomeration of HA, hence enhancing the size exclusion of CuFeCM. Meanwhile, oxidized HA particles with changing physicochemical properties reduced the total attractive interaction energy between CuFeCM and HA, mainly attributed to the reduced acid-base interaction energy according to the Extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) analysis. The changing of HA properties and HA-CuFeCM physicochemical interactions rendered more re-agglomerated HA particles retained above membrane with less attachment, which induced decreasing irreversible fouling resistance and facilitated easier external fouling removal by hydraulic cleaning. Overall, the PMS/CuFeCM configuration demonstrated in this study could provide a new insight into the synergistic oxidation - filtration interaction mechanism of hybrid catalytic ceramic membrane filtration process.