Performance of TiO2-Based Tubular Membranes in the Photocatalytic Degradation of Organic Compounds.

This work presents the photocatalytic degradation of organic pollutants in water with TiO2 and TiO2/Ag membranes prepared by immobilising photocatalysts on ceramic porous tubular supports. The permeation capacity of TiO2 and TiO2/Ag membranes was checked before the photocatalytic application, showing high water fluxes (≈758 and 690 L m-2 h-1 bar-1, respectively) and <2% rejection against the model pollutants sodium dodecylbenzene sulfonate (DBS) and dichloroacetic acid (DCA). When the membranes were submerged in the aqueous solutions and irradiated with UV-A LEDs, the photocatalytic performance factors for the degradation of DCA were similar to those obtained with suspended TiO2 particles (1.1-fold and 1.2-fold increase, respectively). However, when the aqueous solution permeated through the pores of the photocatalytic membrane, the performance factors and kinetics were two-fold higher than for the submerged membranes, mostly due to the enhanced contact between the pollutants and the membranes photocatalytic sites where reactive species were generated. These results confirm the advantages of working in a flow-through mode with submerged photocatalytic membranes for the treatment of water polluted with persistent organic molecules, thanks to the reduction in the mass transfer limitations.

Antibacterial properties of photochemically prepared AgTiO2 membranes.

Biofouling reduces the membrane performance and has become a problem in many applications. One of the strategies to reduce biofouling is to apply antibacterial materials to the membrane surface, which prevents the attachment and growth of microorganisms. In this study, the surface of flat ceramic supports was covered with TiO2 powder, and silver was applied by photoreduction using a CH3COOAg solution at room temperature. After the photoreduction, AgOx and metallic silver were found on the TiO2 as analyzed by XPS. While a negligible amount of silver was released from the prepared AgTiO2 membranes into water, the dissolution of silver was enhanced in a 0.09 M NaCl solution. The AgTiO2 membranes inhibited the growth of Escherichia coli in dark conditions. The inhibition cannot be explained only by the concentration of silver ions released from the membranes. Microscopic observation showed that direct contact with AgTiO2 kills E. coli. The results showed the possibility of improving the antibacterial activity of membranes by applying an AgTiO2 coating.

Influence of Salts on the Photocatalytic Degradation of Formic Acid in Wastewater.

Conventional wastewater treatment technologies have difficulties in feasibly removing persistent organics. The photocatalytic oxidation of these contaminants offers an economical and environmentally friendly solution. In this study, TiO2 membranes and Ag/TiO2 membranes were prepared and used for the decomposition of dissolved formic acid in wastewater. The photochemical deposition of silver on a TiO2 membrane improved the decomposition rate. The rate doubled by depositing ca. 2.5 mg of Ag per 1 g of TiO2. The influence of salinity on formic acid decomposition was studied. The presence of inorganic salts reduced the treatment performance of the TiO2 membranes to half. Ag/TiO2 membranes had a larger reduction of ca. 40%. The performance was recovered by washing the membranes with water. The anion adsorption on the membrane surface likely caused the performance reduction.

Impact of Ionic Liquid Structure and Loading on Gas Sorption and Permeation for ZIF-8-Based Composites and Mixed Matrix Membranes.

Carbon dioxide (CO2) capture has become of great importance for industrial processes due to the adverse environmental effects of gas emissions. Mixed matrix membranes (MMMs) have been studied as an alternative to traditional technologies, especially due to their potential to overcome the practical limitations of conventional polymeric and inorganic membranes. In this work, the effect of using different ionic liquids (ILs) with the stable metal-organic framework (MOF) ZIF-8 was evaluated. Several IL@ZIF-8 composites and IL@ZIF-8 MMMs were prepared to improve the selective CO2 sorption and permeation over other gases such as methane (CH4) and nitrogen (N2). Different ILs and two distinct loadings were prepared to study not only the effect of IL concentration, but also the impact of the IL structure and affinity towards a specific gas mixture separation. Single gas sorption studies showed an improvement in CO2/CH4 and CO2/N2 selectivities, compared with the ones for the pristine ZIF-8, increasing with IL loading. In addition, the prepared IL@ZIF-8 MMMs showed improved CO2 selective behavior and mechanical strength with respect to ZIF-8 MMMs, with a strong dependence on the intrinsic IL CO2 selectivity. Therefore, the selection of high affinity ILs can lead to the improvement of CO2 selective separation for IL@ZIF-8 MMMs.

Single Gas Permeance Performance of High Silica SSZ-13 Zeolite Membranes.

Continuous and high silica SSZ-13 zeolite membranes were prepared on porous mullite supports from high SiO2/Al2O3 ratio or aluminum-free precursor synthesis gel. Single gas permeance (CO2 and CH4) of the high silica SSZ-13 zeolite membrane was decreased with the SiO2/Al2O3 ratio in the precursor synthesis gel, while the ideal CO2/CH4 selectivity of the membrane was gradually increased. Moreover, effects of synthesis conditions (such as H2O/SiO2 and RNOH/SiO2 ratios of precursor synthesis gel, crystallization time) on the single gas permeance performance of high silica SSZ-13 zeolite membranes were studied in detail. Medium H2O/SiO2 and RNOH/SiO2 ratios in the initial synthesis gel were crucial to prepare the good CO2 perm-selective SSZ-13 zeolite membrane. When the molar composition of precursor synthesis gel, crystallization temperature and time were 1.0 SiO2: 0.1 Na2O: 0.1 TMAdaOH: 80 H2O, 160 °C and 48 h, CO2 permeance and ideal CO2/CH4 selectivity of the SSZ-13 zeolite membrane were 0.98 × 10-7 mol/(m²·s·Pa) and 47 at 25 °C and 0.4 MPa. In addition, the SiO2/Al2O3 ratio of the corresponding SSZ-13 zeolite was 410 by X-ray fluorescence spectroscopy.

Photocatalytic activity of titanium dioxide modified by silver nanoparticles.

Photocatalytic activity of Ag/TiO(2) composites obtained by photoreduction treatment (PRT) was investigated. The composite materials, containing various ratio of silver nanoparticles (0.6-3.7 wt %) were obtained by depositing silver on the Evonic-Degussa P25 titania surface. Selected samples whose color varied between light rose and purple brown were examined by SEM, TEM, XPS, DRS, and BET techniques. Flat band potential was determined using Roy method. TEM analysis showed spherically shaped silver nanoparticles of the diameter 4-12 nm. The XPS measurements revealed that silver particles were obtained mainly in metallic form. DRS spectra and photovoltage measurements showed that silver nanoparticles modified the P25 spectral properties but they changed neither the band gap nor the location of flat band potential. The photocatalytic activity of Ag/P25 composite was compared to the photocatalytic activity of pure P25 in the photooxidation reaction of an important potable water contaminant humic acid (HA) and two model compounds, oxalic acid (OxA) and formic acid (FA). The photodecomposition reaction was investigated in a batch reactor containing aqueous suspension of a photocatalyst illuminated by either UV or artificial sunlight (halogen lamp). The tests proved that a small amount of silver nanoparticles deposited on the titania surface triggers the increase in photocatalytic activity; this increase depends, however, on the decomposed substance.