Synergistic control of urban heat island and urban pollution island effects using green infrastructure.

Urban heat island (UHI) and urban pollution island (UPI) effects are two major challenges that affect the liveability and sustainability of cities under the circumstance of climate change. However, existing studies mostly addressed them separately. Urban green infrastructure offers nature-based solutions to alleviate urban heat, enhance air quality and promote sustainability. This review paper provides a comprehensive synthesis of the roles of urban green spaces, street trees, street hedges, green roofs and vertical greenery in mitigating UHI and UPI effects. These types of green infrastructure can promote the thermal environment and air quality, but also potentially lead to conflicting impacts. Medium-sized urban green spaces are recommended for heat mitigation because they can provide a balance between cooling efficiency and magnitude. Conversely, street trees pose a complex challenge since they can provide cooling through shading and evapotranspiration while hindering pollutant dispersion due to reduced air ventilation. Integrated research that considers simultaneous UHI and UPI mitigation using green infrastructure, their interaction with building features, and the urban geographical environment is crucial to inform urban planning and maximize the benefits of green infrastructure installations.

In Situ-Generated Reactive Oxygen Species in Precharged Titania and Tungsten Trioxide Composite Catalyst Membrane Filters: Application to As(III) Oxidation in the Absence of Irradiation.

This study demonstrates that in situ-generated reactive oxygen species (ROSs) in prephotocharged TiO2 and WO3 (TW) composite particle-embedded inorganic membrane filters oxidize arsenite (As(III)) into arsenate (As(V)) without any auxiliary chemical oxidants under ambient conditions in the dark. TW membrane filters have been charged with UV or simulated sunlight and subsequently transferred to a once-through flow-type system. The charged TW filters can transfer the stored electrons to dissolved O2, producing ROSs that mediate As(III) oxidation in the dark. Dramatic inhibition of As(V) production with O2 removal or addition of ROS quenchers indicates an ROS-mediated As(III) oxidation mechanism. Electron paramagnetic spectroscopic analysis has confirmed the formation of the HO2•/O2•- pair in the dark. The WO3 fraction in the TW filter significantly influences the performance of the As(III) oxidation, while As(V) production is enhanced with increasing charging time and solution pH. The As(III) oxidation is terminated when the singly charged TW filter is fully discharged; however, recharging of TW recovers the catalytic activity for As(III) oxidation. The proposed oxidation process using charged TW membrane filters is practical and environmentally benign for the continuous treatment of As(III)-contaminated water during periods of unavailability of sunlight.

Simultaneous nitrification-denitrification using baffled osmotic membrane bioreactor-microfiltration hybrid system at different oxic-anoxic conditions for wastewater treatment.

The efficacy of a baffled osmotic membrane bioreactor-microfiltration (OMBR-MF) hybrid system equipped with thin film forward osmosis membrane for wastewater treatment was evaluated at laboratory scale. The novel OMBR-MF hybrid system involved baffles, that separate oxic and anoxic zones in the aerobic reactor for simultaneous nitrification and denitrification (SND), and a bioreactor comprised of thin film composite-forward osmosis (TFC-FO) and polyether sulfone-microfiltration (PES-MF) membranes. The evaluation was conducted under four different oxic-anoxic cycle patterns. Changes in flux, salinity build-up, and microbial activity (e.g., extracellular polymeric substances (EPS) were assessed. Over the course of a 34 d test, the OMBR-MF hybrid system achieved high removal of total organic carbon (TOC) (86-92%), total nitrogen (TN) (63-76%), and PO4-P (57-63%). The oxic-anoxic cycle time of 0.5-1.5 h was identified to be the best operating condition. Incorporation of MF membrane effectively alleviated salinity build-up in the reactor, allowing stable system operation.

TiO2-Coated Optical Fibres for Groundwater Remediation.

In this study, polyethylene glycol (PEG) was tested as an alternative polymer to improve the coating of TiO2 particles onto optical fibres. The addition of PEG helped dispersing effectively the particles in solution to control their deposition and therefore achieving better properties of the coating film. Results showed that PEG increased the effectiveness of the coating and the prepared fibres showed better performance for the removal of methylene blue (MB). This was attributed to the morphological changes induced by PEG. EDX mapping of the fibre surface showed that the addition of PEG lead to a better coverage of the fibre surface; increasing the active surface area for subsequent photocatalytic degradation. This study also showed that the light intensity, pH and initial concentration of MB have a significant influence. Finally, it was demonstrated that the coatings using PEG were better ordered and structured; showing a distinct layer-by-layer deposition.

Removal behaviors and fouling mechanisms of charged antibiotics and nanoparticles on forward osmosis membrane.

Fouling and rejection mechanisms of both charged antibiotics (ABs) and nanoparticles (NPs) were determined using a negatively-charged polyamide thin film composite forward osmosis (FO) flat sheet membrane. Two types of ABs and NPs were selected as positively and negatively charged foulants at pH 8. The ABs did not cause significant membrane fouling, but the extent of fouling and rejection changed based on the electrostatic attraction or repulsion forces. The addition of opposite charged AB and NP resulted in a decline of the membrane flux by 11.0% but a 6.5% AB average rejection efficiency improvement. On the other hand, mixing of like-charged ABs and NPs generated repulsive forces that improved average rejection efficiency about 5.5% but made no changes in the membrane flux. In addition, NPs and ABs were mixed and tested at various concentrations and pH levels to rectify the behavior of ABs. The aggregate size and removal efficiency were observed to vary with the change in the electron double layer of the mixture. It can help to make the strategy to control the ABs in the FO process and consequently it enables the FO process to produce environmentally safe effluent.

Understanding the organic micropollutants transport mechanisms in the fertilizer-drawn forward osmosis process.

We systematically investigated the transport mechanisms of organic micropollutants (OMPs) in a fertilizer-drawn forward osmosis (FDFO) membrane process. Four representative OMPs, i.e., atenolol, atrazine, primidone, and caffeine, were chosen for their different molecular weights and structural characteristics. All the FDFO experiments were conducted with the membrane active layer on the feed solution (FS) side using three different fertilizer draw solutions (DS): potassium chloride (KCl), monoammonium phosphate (MAP), and diammonium phosphate (DAP) due to their different properties (i.e., osmotic pressure, diffusivity, viscosity and solution pH). Using KCl as the DS resulted in both the highest water flux and the highest reverse solute flux (RSF), while MAP and DAP resulted in similar water fluxes with varying RSF. The pH of the FS increased with DAP as the DS due to the reverse diffusion of NH4+ ions from the DS toward the FS, while for MAP and DAP DS, the pH of the FS was not impacted. The OMPs transport behavior (OMPs flux) was evaluated and compared with a simulated OMPs flux obtained via the pore-hindrance transport model to identify the effects of the OMPs structural properties. When MAP was used as DS, the OMPs flux was dominantly influenced by the physicochemical properties (i.e., hydrophobicity and surface charge). Those OMPs with positive charge and more hydrophobic, exhibited higher forward OMP fluxes. With DAP as the DS, the more hydrated FO membrane (caused by increased pH) as well as the enhanced RSF hindered OMPs transport through the FO membrane. With KCl as DS, the structural properties of the OMPs were dominant factors in the OMPs flux, however the higher RSF of the KCl draw solute may likely hamper the OMPs transport through the membrane especially those with higher MW (e.g., atenolol). The pore-hindrance model can be instrumental in understanding the effects of the hydrodynamic properties and the surface properties on the OMPs transport behaviors.

Volatile fatty acids and biogas recovery using thermophilic anaerobic membrane distillation bioreactor for wastewater reclamation.

The effects of bioreactor temperatures and salinities of an anaerobic membrane distillation bioreactor (anMDBR) on the permeation performance and their potential recovery of bioresources were fully examined in this study. To the best of our knowledge, this is the first study of a lab-scale anMDBR process utilizing sub-merged hollow fiber membranes. The hybrid system utilizing both membrane distillation (MD) and anaerobic bioreactors achieved 99.99% inorganic salt rejection regardless the operation temperatures and high initial flux from (2-4 L m-2 h-1) at 45-65 °C. However, after 7-day operation, the flux dropped by 16-50% proportional to the bioreactor temperatures. It was found that the effects of bioreactor temperatures had strong impacts on both the permeation performance and fouling behavior while salinity had insignificant effect. A compact non-porous fouling layer was observed on the membrane surface from the bioreactor operated at 65 °C while only a few depositions was found on the membrane from 45 °C bioreactor. In the present study, the optimal anMDBR temperature was found to be 45 °C, showing a balanced biogas production and membrane permeation performance including less fouling formation. At this bioreactor temperature (45 °C), the biogas yield was 0.14 L/g CODremoval, while maintaining a methane recovery of 42% in the biogas, similar recovery to those at bioreactor temperatures of 55 and 65 °C. The potential recovery of volatile fatty acids made anMDBR a more economically efficient system, in addition to its lower operation cost and smaller footprint compared with most other technologies for on-site wastewater treatment.

Preparation and characterization of TiO2 generated from synthetic wastewater using TiCl4 based coagulation/flocculation aided with Ca(OH)2.

This study focused on the preparation of undoped and Ca-doped titania from flocculation generated sludge. Initially, TiCl4 was utilised to perform coagulation and flocculation in synthetic wastewater and an optimised dose of coagulant was determined by evaluating the turbidity, dissolved organic carbon (DOC) and zeta potential of the treated water. Later, using Ca(OH)2 as a coagulant aid, the effects on effluent pH, turbidity and DOC removal were investigated. Both Ca-doped and undoped anatase TiO2 were prepared from the flocculated sludge for morphological and photocatalytic evaluation. During the standalone use of TiCl4, maximum turbidity and DOC removal were found at 11.63 and 14.54 mg Ti/L, respectively. At the corresponding coagulant dose, rapid deprotonation of water caused the pH of the effluent to reach below 3.77 mg Ti/L. Whereas, when using Ca(OH)2 as a coagulant aid, a neutral pH (7.26) was attained at a simultaneous dosing of 32.40 mg Ca/L and 14.54 mg Ti/L. When aided with Ca(OH)2, the turbidity removal was further increased by 54.28% and the DOC removal was somewhat similar to the standalone use of TiCl4. TiO2 was prepared by incinerating the collected sludge at 600 °C for 2 h. Both XRD and SEM analysis were conducted to observe the morphology of the prepared titania. The XRD pattern of the TiO2 showed only an anatase phase along with the presence of a high atomic proportion of Ca (4.14%). Consequently, a high amount of Ca atoms inhibited the level of TiO2 phase and no obvious presence of CaO was observed. The prepared Ca-doped TiO2 at the optimised dose of Ca(OH)2 was found to be inferior to the undoped TiO2 during the photodegradation of acetaldehyde. However, a reduced dose of Ca(OH)2 (<15 mg Ca/L) exhibited a substantial increase in photoactivity under UV irradiance.

Removal of fluoride in membrane-based water and wastewater treatment technologies: Performance review.

The presence of excess fluoride in aqueous media above local environmental standards (e.g., the U.S. Environmental Protection Agency (EPA) standard of 4 mg/L) affects the health of aquatic life. Excess fluoride in drinking water above the maximum contaminant level (e.g., the World Health Organization (WHO) standard of 1.5 mg/L) also affects the skeletal and nervous systems of humans. Fluoride removal from aqueous solutions is difficult using conventional electrochemical, precipitation, and adsorption methods owing to its ionic size and reactivity. Thus, new technologies have been introduced to reduce the fluoride concentration in industrial wastewater effluents and various drinking water sources. Membrane technology is one of the newer technologies found to be very effective in significantly reducing fluoride to desired standards levels; however, it has received less attention than other technologies because it is perceived as a costly process. This study critically reviewed the performance of various membrane process and compared it with effluent and zero liquid discharge (ZLD) standards. The performance review has been conducted with the consideration of the theoretical background, rejection mechanisms, technical viability, and parameters affecting flux and rejection performance. This review includes membrane systems investigated for the defluoridation process but operated under pressure (i.e., reverse osmosis [RO] and nanofiltration [NF]), temperature gradients (i.e., membrane distillation [MD]), electrical potential gradients (i.e., electrodialysis [ED] and Donnan dialysis [DD]), and concentration differences (i.e., forward osmosis [FO]). Moreover, the study also addressed the advantages, limitations, & applicable conditions of each membrane based defluoridation process.

Core-Shell Interface-Oriented Synthesis of Bowl-Structured Hollow Silica Nanospheres Using Self-Assembled ABC Triblock Copolymeric Micelles.

Hollow porous silica nanospheres (HSNs) are emerging classes of cutting-edge nanostructured materials. They have elicited much interest as carriers of active molecule delivery due to their amorphous chemical structure, nontoxic nature, and biocompatibility. Structural development with hierarchical morphology is mostly required to obtain the desired performance. In this context, large through-holes or pore openings on shells are desired so that the postsynthesis loading of active-molecule onto HSNs via a simple immersion method can be facilitated. This study reports the synthesis of HSNs with large through-holes or pore openings on shells, which are subsequently termed bowl-structured hollow porous silica nanospheres (BHSNs). The synthesis of BHSNs was mediated by the core-shell interfaces of the core-shell corona-structured micelles obtained from a commercially available ABC triblock copolymer (polystyrene- b-poly(2-vinylpyridine)- b-poly(ethylene oxide) (PS-P2VP-PEO)). In this synthesis process, polymer@SiO2 composite structure was formed because of the deposition of silica (SiO2) on the micelles' core. The P2VP block played a significant role in the hydrolysis and condensation of the silica precursor, i.e., tetraethylorthosilicate (TEOS) and then maintaining the shell's growth. The PS core of the micelles built the void spaces. Transmission electron microscopy (TEM) images revealed a spherical hollow structure with an average particle size of 41.87 ± 3.28 nm. The average diameter of void spaces was 21.71 ± 1.22 nm, and the shell thickness was 10.17 ± 1.68 nm. According to the TEM image analysis, the average large pore was determined to be 15.95 nm. Scanning electron microscopy (SEM) images further confirmed the presence of large single pores or openings in shells. These were formed as a result of the accumulated ethanol on the PS core acting to prevent the growth of silica.

Hierarchical Composite Membranes with Robust Omniphobic Surface Using Layer-By-Layer Assembly Technique.

In this study, composite membranes were fabricated via layer-by-layer (LBL) assembly of negatively charged silica aerogel (SiA) and 1H,1H,2H,2H-perfluorodecyltriethoxysilane (FTCS) on a polyvinylidene fluoride phase inversion membrane and interconnecting them with positively charged poly(diallyldimethylammonium chloride) (PDDA) via electrostatic interaction. The results showed that the PDDA-SiA-FTCS coated membrane had significantly enhanced the membrane structure and properties. New trifluoromethyl and tetrafluoroethylene bonds appeared at the surface of the coated membrane, which led to lower surface free energy of the composite membrane. Additionally, the LBL membrane showed increased surface roughness. The improved structure and property gave the LBL membrane an omniphobic property, as indicated by its good wetting resistance. The membrane performed a stable air gap membrane distillation (AGMD) flux of 11.22 L/m2 h with very high salt rejection using reverse osmosis brine from coal seam gas produced water as feed with the addition of up to 0.5 mM SDS solution. This performance was much better compared to those of the neat membrane. The present study suggests that the enhanced membrane properties with good omniphobicity via LBL assembly make the porous membranes suitable for long-term AGMD operation with stable permeation flux when treating challenging saline wastewater containing low surface tension organic contaminants.

Nanostructured Biomass Based Carbon Materials from Beer Lees for Hydrogen Storage.

The present work describes the preparation of carbon materials from beer lees and their hydrogen adsorption abilities. Activated carbons (ACs) from beer lees were prepared through chemical activation using potassium hydroxide as an activating agent. The low temperature nitrogen adsorption isotherm studies on prepared ACs were conducted at 77 K to determine their physical properties and adsorption energy distribution. The beer lees based carbons have energetically heterogeneous surfaces and high surface area ranging from 1927-2408 m2/g. ACs prepared in this study show the gravimetric hydrogen adsorption capacity of 2.43-2.92 wt% depending on their physical properties.

Combining high performance fertiliser with surfactants to reduce the reverse solute flux in the fertiliser drawn forward osmosis process.

Solutions to mitigate the reverse diffusion of solutes are critical to the successful commercialisation of the fertiliser drawn forward osmosis process. In this study, we proposed to combine a high performance fertiliser (i.e., ammonium sulfate or SOA) with surfactants as additives as an approach to reduce the reverse diffusion of ammonium ions. Results showed that combining SOA with both anionic and non-ionic surfactants can help in reducing the reverse salt diffusion by up to 67%. We hypothesised that, hydrophobic interactions between the surfactant tails and the membrane surface likely constricted membrane pores resulting in increased rejection of ions with large hydrated radii such as SO42-. By electroneutrality, the rejection of the counter ions (i.e., NH4+) also therefore subsequently improved. Anionic surfactant was found to further decrease the reverse salt diffusion due to electrostatic repulsions between the surfactant negatively-charged heads and SO42-. However, when the feed solution contains cations with small hydrated radii (e.g., Na+); it was found that NH4+ ions can be substituted in the DS to maintain its electroneutrality and thus the diffusion of NH4+ to the feed solution was increased.

Computing the effective diffusion coefficient of solutes in a multi-salts solutions during forward osmosis (FO) membrane filtration: Experiments and mathematical modelling.

Diffusion coefficient of solutes through a porous membrane media is different from diffusion coefficient through a free homogenous media. Porosity, tortuosity and the thickness of the membrane significantly affect the diffusion through a specific thickness of a membrane and therefore it is termed as effective diffusion coefficient (Deff) which is lower than the actual diffusion coefficient, D. The Deff of single or dual solutes through a porous membrane layer are well documented but not for multiple salts. Therefore, in this study, single, dual and multiple salt mixtures were passed through a flat sheet cellulose triacetate Forward Osmosis (FO) membrane to obtain a semi-empirical relationship with the Deff and its water flux. This will allow computing the structural coefficient of FO membranes. Research community have spent tremendous efforts in membrane modification to reduce the structural coefficient to improve FO process efficiency. Our finding suggests that optimising the draw solution chemistry can achieve this goal.

Engineering the Re-Entrant Hierarchy and Surface Energy of PDMS-PVDF Membrane for Membrane Distillation Using a Facile and Benign Microsphere Coating.

To consolidate the position of membrane distillation (MD) as an emerging membrane technology that meets global water challenges, it is crucial to develop membranes with ideal material properties. This study reports a facile approach for a polyvinylidene fluoride (PVDF) membrane surface modification that is achieved through the coating of the surface with poly(dimethylsiloxane) (PDMS) polymeric microspheres to lower the membrane surface energy. The hierarchical surface of the microspheres was built without any assistance of a nano/microcomposite by combining the rapid evaporation of tetrahydrofuran (THF) and the phase separation from condensed water vapor. The fabricated membrane exhibited superhydrophobicity-a high contact angle of 156.9° and a low contact-angle hysteresis of 11.3°-and a high wetting resistance to seawater containing sodium dodecyl sulfate (SDS). Compared with the control PVDF-hexafluoropropylene (HFP) single-layer nanofiber membrane, the proposed fabricated membrane with the polymeric microsphere layer showed a smaller pore size and higher liquid entry pressure (LEP). When it was tested for the direct-contact MD (DCMD) in terms of the desalination of seawater (3.5% of NaCl) containing SDS of a progressively increased concentration, the fabricated membrane showed stable desalination and partial wetting for the 0.1 and 0.2 mM SDS, respectively.

Evaluation of fertilizer-drawn forward osmosis for sustainable agriculture and water reuse in arid regions.

The present study focused on the performance of the FDFO process to achieve simultaneous water reuse from wastewater and production of nutrient solution for hydroponic application. Bio-methane potential (BMP) measurements were firstly carried out to determine the effect of osmotic concentration of wastewater achieved in the FDFO process on the anaerobic activity. Results showed that 95% water recovery from the FDFO process is the optimum value for further AnMBR treatment. Nine different fertilizers were then tested based on their FO performance (i.e. water flux, water recovery and reverse salt flux) and final nutrient concentration. From this initial screening, ammonium phosphate monobasic (MAP), ammonium sulfate (SOA) and mono-potassium phosphate were selected for long term experiments to investigate the maximum water recovery achievable. After the experiments, hydraulic membrane cleaning was performed to assess the water flux recovery. SOA showed the highest water recovery rate, up to 76% while KH2PO4 showed the highest water flux recovery, up to 75% and finally MAP showed the lowest final nutrient concentration. However, substantial dilution was still necessary to comply with the standards for fertigation even if the recovery rate was increased.

Adsorption and Photocatalytic Degradation of Methylene Blue Using Potassium Polytitanate and Solar Simulator.

Solar photocatalytic degradation of organic water pollutants can be used to degrade toxic organic pollutants in water. In this study, potassium titanate nanofibres were synthesized by an aqueous peroxide route at high pH and examined as photocatalysts for photodegradation of methylene blue (MB) using a solar simulator. Initially, MB was adsorbed on the surface of potassium polytitanates to achieve adsorption equilibrium before the photocatalysts were illuminated using solar simulator. The results showed that potassium polytitanate nanofibres were effective adsorbents of MB and also facilitated its photocatalytic degradation. Sulphate ion evolution during photocatalysis confirmed that some mineralisation occurred and hence photo-oxidative degradation of MB took place. The optimum operational conditions for the photocatalytic degradation of MB were found at 0.05 g/L of photocatalyst load, 10 mg/L MB and pH 7. The stability and regeneration of the photocatalyst specimen was also studied for 3 degradation cycles using adsorption/photocatalysis model. Morphological structure analysis of potassium titanate showed nanocrystallines structure of longitudinally-oriented isolated fibre with a length up to several micrometres with diameters ranging from 10 to 20 nanometres.

Fatty acid fouling of forward osmosis membrane: Effects of pH, calcium, membrane orientation, initial permeate flux and foulant composition.

Octanoic acid (OA) was selected to represent fatty acids in effluent organic matter (EOM). The effects of feed solution (FS) properties, membrane orientation and initial permeate flux on OA fouling in forward osmosis (FO) were investigated. The undissociated OA formed a cake layer quickly and caused the water flux to decline significantly in the initial 0.5hr at unadjusted pH3.56; while the fully dissociated OA behaved as an anionic surfactant and promoted the water permeation at an elevated pH of 9.00. Moreover, except at the initial stage, the sudden decline of water flux (meaning the occurrence of severe membrane fouling) occurred in two conditions: 1. 0.5mmol/L Ca(2+), active layer facing draw solution (AL-DS) and 1.5mol/L NaCl (DS); 2. No Ca(2+), active layer-facing FS (AL-FS) and 4mol/L NaCl (DS). This demonstrated that cake layer compaction or pore blocking occurred only when enough foulants were absorbed into the membrane surface, and the water permeation was high enough to compact the deposit inside the porous substrate. Furthermore, bovine serum albumin (BSA) was selected as a co-foulant. The water flux of both co-foulants was between the fluxes obtained separately for the two foulants at pH3.56, and larger than the two values at pH9.00. This manifested that, at pH3.56, BSA alleviated the effect of the cake layer caused by OA, and OA enhanced BSA fouling simultaneously; while at pH9.00, the mutual effects of OA and BSA eased the membrane fouling.

Titania produced from Ti-salt flocculated sludge: photocatalytic activity under solar light.

In this study, titania photocatalyst was produced from the wastewater sludge of Ti-salt flocculation. The high photocatalytic activity of titania reported was evaluated based on a single organic substrate. However, the photocatalytic activity is a substrate-specific; one photocatalyst showed different photocatalytic degradation rates for different substrates. Thus, to investigate the substrate-specific photocatalytic activity of titania, various substrates of humic acid (HA), dichloroacetic acid (DCA), rhodamine B (RhB), metsulfuron methyl (M&M) and phenol were used under simulated solar light irradiation. Results showed titania had a high activity rate for RhB, moderate activity for HA and DCA and low activity for M&M and phenol indicating substrate-specific activities. When compared with Degussa-P25, titania showed higher activity for M&M, while the opposite was observed for HA and phenol. The specific-substrate behaviour of titania could depend on specific physicochemical and electronic interactions between titania, substrates, and their intermediates compounds formed.

Synthesis and characterisation of potassium polytitanate for photocatalytic degradation of crystal violet.

Potassium titanate nanostructures were synthesised by hydrothermal treatment of TiO2 (P25) in KOH and H2O2. As-produced powders were characterised by scanning electron microscopy, energy-dispersive X-ray spectroscopy, transmission electron microscopy, X-ray diffraction, and nitrogen adsorption-desorption methods. Longitudinally-oriented-wire-like structures with a length up to several micrometres and diameters ranging from 10 to 30 nm were obtained. Larger size fibrous nanowires resulting from the hydrothermal treatment showed high affinity in adsorbing crystal violet (CV), which was mainly due to their high surface area. The photocatalytic bleaching of CV solution revealed that the wires are photoactive under ultraviolet light irradiation. Macroporous nanowires are considered as effective adsorbents of CV, capable of photocatalytic degradation, and they can be easily separated from the solution by settling.