Fouling and inactivation of titanium dioxide-based photocatalytic systems

Copyright © 2015 Taylor & Francis Group, LLC. Titanium dioxide is an effective photocatalyst for the breakdown of many environmental contaminants. The complex mixtures that can occur in water matrices can significantly affect the breakdown of the contaminants in water by titanium dioxide (TiO2). The authors discuss a wide variety of foulants and inhibitors of photocatalytic TiO2 systems and review different methods that can be effective for their fouling prevention. Approaches to regenerate a fouled or contaminated TiO2 catalysts are explored and the effect of substrates on immobilized titanium dioxide is also reviewed

Stability of Fe-oxide nanoparticles coated with natural organic matter under relevant environmental conditions

© IWA Publishing 2014 Manufactured nanoparticles (MNPs) are increasingly released into the environment and thus research on their fate and behaviour in complex environmental samples is urgently needed. The fate of MNPs in the aquatic environment will mainly depend on the physico-chemical characteristics of the medium. The presence and concentration of natural organic matter (NOM) will play a significant role on the stability of MNPs by either decreasing or exacerbating the aggregation phenomenon. In this study, we firstly investigated the effect of NOM concentration on the aggregation behaviour of manufactured Fe-oxide nanoparticles. Then, the stability of the coated nanoparticles was assessed under relevant environmental conditions. Flow field-flow fractionation, an emerging method which is gaining popularity in the field of nanotechnology, has been employed and results have been compared to another size-measurement technique to provide increased confidence in the outcomes. Results showed enhanced stability when the nanoparticles are coated with NOM, which was due to electrosteric stabilisation. However, the presence of divalent cations, even at low concentration (i.e. less than 1 mM) was found to induce aggregation of NOM-coated nanoparticles via bridging mechanisms between NOM and Ca2+

Agglomeration behaviour of titanium dioxide nanoparticles in river waters: A multi-method approach combining light scattering and field-flow fractionation techniques

© 2015 Elsevier Ltd. Titanium dioxide nanoparticles (TiO2 NPs) are currently one of the most prolifically used nanomaterials, resulting in an increasing likelihood of release to the environment. This is of concern as the potential toxicity of TiO2 NPs has been investigated in several recent studies. Research into their fate and behaviour once entering the environment is urgently needed to support risk assessment and policy development. In this study, we used a multi-method approach combining light scattering and field-flow fractionation techniques to assess both the aggregation behaviour and aggregate structure of TiO2 NPs in different river waters. Results showed that both the aggregate size and surface-adsorbed dissolved organic matter (DOM) were strongly related to the initial DOM concentration of the tested waters (i.e. R2>0.90) suggesting that aggregation of TiO2 NPs is controlled by the presence and concentration of DOM. The conformation of the formed aggregates was also found to be strongly related to the surface-adsorbed DOM (i.e. R2>0.95) with increasing surface-adsorbed DOM leading to more compact structures. Finally, the concentration of TiO2 NPs remaining in the supernatant after sedimentation of the larger aggregates was found to decrease proportionally with both increasing IS and decreasing DOM concentration, resulting in more than 95% sedimentation in the highest IS sample

Modification of nanofiber support layer for thin film composite forward osmosis membranes via layer-by-layer polyelectrolyte deposition

© 2018 by the authors. Licensee MDPI, Basel, Switzerland. Electrospun nanofiber-supported thin film composite membranes are among the most promising membranes for seawater desalination via forward osmosis. In this study, a high-performance electrospun polyvinylidenefluoride (PVDF) nanofiber-supported thin film composite (TFC) membrane was successfully fabricated after molecular layer-by-layer polyelectrolyte deposition. Negatively-charged electrospun polyacrylic acid (PAA) nanofibers were deposited on electrospun PVDF nanofibers to form a support layer consisted of PVDF and PAA nanofibers. This resulted to a more hydrophilic support compared to the plain PVDF nanofiber support. The PVDF-PAA nanofiber support then underwent a layer-by-layer deposition of polyethylenimine (PEI) and PAA to form a polyelectrolyte layer on the nanofiber surface prior to interfacial polymerization, which forms the selective polyamide layer of TFC membranes. The resultant PVDF-LbL TFC membrane exhibited enhanced hydrophilicity and porosity, without sacrificing mechanical strength. As a result, it showed high pure water permeability and low structural parameter values of 4.12 L m−2 h−1 bar−1 and 221 µm, respectively, significantly better compared to commercial FO membrane. Layer-by-layer deposition of polyelectrolyte is therefore a useful and practical modification method for fabrication of high performance nanofiber-supported TFC membrane

Thin-film composite membrane on a compacted woven backing fabric for pressure assisted osmosis

© 2016 Elsevier B.V. The water flux in forward osmosis (FO) process declines substantially when the draw solution (DS) concentration reaches closer to the point of osmotic equilibrium with the feed solution (FS). Using external hydraulic pressure alongside the osmotic driving force in the pressure assisted osmosis (PAO) has been found effective in terms of enhancing water flux and even potentially diluting the DS beyond osmotic equilibrium. The net gain in water flux due to the applied pressure in the PAO process closely depends on the permeability of the FO membrane. The commercial flat sheet cellulose triacetate (CTA) FO membrane has low water permeability and hence the effective gain in water flux in the PAO process is low. In this study, a high performance thin film composite membrane was developed especially for the PAO process through casting polyethersulfone (PES) polymer solution on a compacted woven fabric mesh support followed by interfacial polymerisation for polyamide active layer. This PAO membrane possesses a water flux of 37 L m2h− 1using 0.5 M NaCl as DS and deionised water as the feed at an applied hydraulic pressure of 10 bar. Besides, the membrane was able to endure the external hydraulic pressure required for the PAO process owing to the embedded backing fabric support. While the membranes with low structural parameters are essential for higher water flux, this study shows that for PAO process, polymeric membranes with larger structural parameters may not be suitable for PAO. They generally resulted in compaction and poor mechanical strength to withstand hydraulic pressure

Coagulation performance and floc characteristics of polytitanium tetrachloride and titanium tetrachloride compared with ferric chloride for coal mining wastewater treatment

© 2015 Elsevier B.V. Abstract The production and discharge of large volumes of wastewater during coal mining activities are one of the major environmental issues in Australia. Therefore, it is crucial to develop and optimise effective treatment processes for the safe disposal of coal mining wastewater (CMWW). In this study, we investigated the performance of a recently developed polytitanium tetrachloride (PTC) coagulant and compared with the performance of titanium tetrachloride (TiCl4) and the commonly used ferric chloride (FeCl3) coagulant for the treatment of CMWW from one of the coal mining sites in Australia. The use of Ti-based coagulants is particularly attractive for the CMWW treatment due to the advantage of being able to recycle the sludge to produce functional titanium dioxide (TiO2) photocatalyst; unlike the flocs formed using conventional coagulants, which need to be disposed in landfill sites. The results showed that both PTC and TiCl4 performed better than FeCl3 in terms of turbidity, UV254 and inorganic compounds (e.g. aluminium, copper or zinc) removal, however, PTC performed poorly in terms of dissolved organic carbon removal (i.e. less than 10%). While charge neutralisation and bridging adsorption were the main coagulation mechanisms identified for TiCl4 treatment; sweep coagulation and bridging adsorption seemed to play a more important role for both PTC and FeCl3 treatments. The flocs formed by PTC coagulation achieved the largest floc size of around 900 μm with the highest floc growth rate. Both Ti-based coagulants (i.e., PTC and TiCl4) showed higher strength factor than FeCl3, while TiCl4 coagulant yielded the flocs with the highest recovery factor. This study indicates that Ti-based coagulants are effective and promising coagulants for the treatment of CMWW

Synthesis and NOx removal performance of anatase S-TiO2/g-CN heterojunction formed from dye wastewater sludge.

In this study, sludges generated from Ti-based flocculation of dye wastewater were used to retrieve photoactive titania (S-TiO2). It was heterojunctioned with graphitic carbon nitride (g-CN) to augment photoactivity under UV/visible light irradiance. Later the as-prepared samples were utilized to remove nitrogen oxides (NOx) in the atmospheric condition through photocatalysis. Heterojunction between S-TiO2 and g-CN was prepared through facile calcination (@550 °C) of S-TiO2 and melamine mix. Advanced sample characterization was carried out and documented extensively. Successful heterojunction was confirmed from the assessment of morphological and optical attributes of the samples. Finally, the prepared samples' level of photoactivity was assessed through photooxidation of NOx under both UV and visible light irradiance. Enhanced photoactivity was observed in the prepared samples irrespective of the light types. After 1 h of UV/visible light-based photooxidation, the best sample STC4 was found to remove 15.18% and 9.16% of atmospheric NO, respectively. In STC4, the mixing ratio of S-TiO2, to melamine was maintained as 1:3. Moreover, the optical bandgap of STC4 was found as 2.65 eV, where for S-TiO2, it was 2.83 eV. Hence, the restrained rate of photogenerated charge recombination and tailored energy bandgap of the as-prepared samples were the primary factors for enhancing photoactivity

Hydrophilic/Hydrophobic Silane Grafting on TiO2 Nanoparticles: Photocatalytic Paint for Atmospheric Cleaning

In this study, anatase titania was utilized to prepare a durable photocatalytic paint with substantially enhanced photoactivity towards NO oxidation. Consequently, to alleviate the choking effect of photocatalytic paint and incorporate self‐cleaning properties, the parent anatase titania was modified with Al(OH)3 and a number of organosilane (tetraethyl orthosilicate, propyltrimethoxysilane, triethoxy(octadecyl)silane, and trimethylchlorosilane) coatings. A facile hydrolysis approach in ethanol was employed to coat the parent titania. To facilitate uniform dispersion in photocatalytic paint and strong bonding with the prevailing organic matrix, it is necessary to avail both hydrophobic and hydrophilic regions on the titania surface. Therefore, during the preparation of modified titania, the weight proportion of the total weight of alkyl silane and trimethylchlorosilane was adjusted to a ratio of 1:1. As the parent titania has few hydrophilic portions on the surface, tetraethyl orthosilicate was coated with an organic silane having an extended alkyl group as a hydrophobic group and tetraethyl orthosilicate as a hydrophilic group. When these two silane mixtures are hydrolyzed simultaneously and coated on the surface of parent titania, a portion containing a large amount of tetraethyl orthosilicate becomes hydrophilic, and a part containing an alkyl silane becomes hydrophobic. The surface morphology and the modified titania’s optical attributes were assessed using X‐ray powder diffraction (XRD), scanning electron microscopy (SEM), energy‐dispersive X‐ray spectroscopy (EDS), UV‐Vis diffuse reflectance spectroscopy (DRS), and electrochemical impedance spectroscopy (EIS) analysis. Based on the advanced characterizations, the NO removal mechanism of the modified titania is reported. The modified titania coated at 20 wt.% on the ceramic substrate was found to remove ~18% of NO under one h of UV irradiation. An extensive UV durability test was also carried out, whereby the coated surface with modified titania was exposed to 350 W/m2 of UV irradiance for 2 weeks. The results indicated that the coated surface appeared to preserve the self‐cleaning property even after oil spraying. Hence, facile hydrolysis of multiple organosilane in ethanol could be a viable approach to design the coating on anatase titania for the fabrication of durable photoactive paint