ABSTRACT
We introduced a modified sol-gel method using polyvinyl alcohol (PVA) as an additive to improve the permeability of γ-Al2O3 membranes by minimizing the thickness of the selective layer and maximizing the porosity. First, the analysis revealed that the thickness of γ-Al2O3 decreased as the concentration of PVA increased in the boehmite sol. Second, the properties of the γ-Al2O3 mesoporous membranes were greatly influenced by the modified route (method B) compared to the conventional route (method A). The results showed that the porosity and surface area of the γ-Al2O3 membrane increased, and the tortuosity decreased considerably using method B. This effect was attributed to the adsorption of PVA molecules on the surface of the boehmite particles, which depended on the synthesis route. The experimentally determined pure water permeability trend and the Hagen-Poiseuille mathematical model confirmed that the modified method improved the performance of the γ-Al2O3 membrane. Finally, the γ-Al2O3 membrane fabricated via a modified sol-gel method with a pore size of 2.7 nm (MWCO = 5300 Da) exhibited a pure water permeability of over 18 LMH/bar, which is three times higher than that of the γ-Al2O3 membrane prepared using the conventional method.
ABSTRACT
Compared to traditional membrane materials, alumina membranes are particularly beneficial for industrial wastewater treatment. However, the development of mesoporous α-alumina membranes for ultrafiltration applications is still a challenge due to uncontrolled pore size. In this study, we optimized the sol-gel method for the fabrication of a high-performance mesoporous α-alumina membrane. The peptization conditions (pH and peptization time) and phase transformation of boehmite were investigated to achieve better properties of the α-alumina membrane. The surface properties of the membrane were observed to be improved by reducing the system pH to 3.5 and increasing the peptization time to 24 h. The effect of sintering temperature on the phase transformation behavior, microstructures and performance of the membranes was also elucidated. An α-alumina ultrafiltration membrane with an average thickness of 2 µm was obtained after sintering at 1100 °C. The molecular weight cut-off of the α-alumina membrane, as obtained by the filtration of aqueous PEG solution, was approximately 163 kDa (12.5 nm). This is the smallest pore size ever reported for pure α-alumina membranes.
ABSTRACT
Numerous reports have elucidated that TiO2 nanoparticles (TiO2-NPs) exhibit respectable photocatalytic degradation capacities due to their high specific surface areas. However, the current recovery process leads to a loss of TiO2-NPs; therefore, there is a need to immobilize TiO2-NPs on the substrate used. Herein, TiO2-coated yttria-stabilized zirconia/silica nanofiber (TiO2-coated YSZ/silica NF) was prepared by coating TiO2 on the surface of YSZ/silica NF using a sol-gel process. The TiO2 coating layer on the nanofiber surface improved the separation ability of the membrane as well as the photocatalytic degradation ability. The pore size of the TiO2-coated YSZ/silica NF membrane was less than that of the pristine YSZ/silica NF membrane, and it rejected over 99.6% of the 0.5 µm polymeric particles. In addition, the TiO2-coated YSZ/silica NF membrane showed excellent adsorption/degradation of humic acid (HA, 88.2%), methylene blue (MB, 92.4%), and tetracycline (TC, 99.5%). Six recycling tests were performed to evaluate the reusability of the TiO2-coated YSZ/silica NF membrane. The adsorption/degradation efficiency for HA, MB, and TC decreased by 3.7%, 2.8%, and 2.2%, respectively. We thus verified the high separation ability, excellent photocatalytic degradation ability, and excellent reusability of the TiO2-coated YSZ/silica NF membranes.
