Highly Efficient Removal of 2,4,5-Trichlorophenoxyacetic Acid by Adsorption and Photocatalysis Using Nanomaterials with Surface Coating by the Cationic Surfactant.

Extensive removal of 2,4,5-trichlorophenoxyacetic acid (2,4,5-T) using titania (TiO2) nanoparticles by adsorption and photocatalysis with a surface coating by cetyltrimethylammonium bromide (CTAB) is reported. The CTAB-coated TiO2 nanoparticles (CCTN) were characterized by FT-IR, zeta-potential measurements, and UV-vis diffuse reflectance spectroscopy (UV-vis-DRS). 2,4,5-T removal increased significantly after surface modification with CTAB compared with bare TiO2 nanoparticles. Optimal parameters affecting 2,4,5-T removal were found to be pH 4, CCTN dosage 10 mg/mL, and adsorption time 180 min. The maximum adsorptive removal of 2,4,5-T using CCTN reached 96.2% while highest adsorption capacity was 13.4 mg/g. CCTN was also found to be an excellent photocatalyst that achieved degradation efficiency of 99.2% with an initial concentration of 25 mg/L. The removal mechanisms of 2,4,5-T using CCTN by both adsorption and photocatalysis are discussed in detail based on changes in functional group vibrations and surface charge. Our results indicate that CCTN is an excellent material for 2,4,5-T removal in water by both adsorption and photocatalysis.

Highly adsorptive removal of ciprofloxacin and E. coli inactivation using amino acid tryptophan modified nano-gibbsite.

Adsorption of essential amino acid, Tryptophan (Tryp) on synthesized gibbsite nanoparticles and their applications in eliminating of antibiotic ciprofloxacin (CFX) and bacteria Escherichia coli (E. coli) in aqueous solution. Nano-gibbsite which was successfully fabricated, was characterized by XRD, TEM-SAED, FT-IR, SEM-EDX and zeta potential measurements. The selected parameters for Tryp adsorption on nano-gibbsite to form biomaterial, Tryp/gibbsite were pH 11, gibbsite dosage 20 mg/mL and 1400 mg/L Tryp. The optimum conditions for CFX removal using Tryp/gibbsite were adsorption time 60 min, pH 5, and 20 mg/mL Tryp/gibbsite dosage. The CFX removal significantly raised from 63 to 90% when using Tryp/gibbsite. The Freundlich and pseudo-second-order models achieved the best fits for CFX adsorption isotherm and kinetic on Tryp/gibbsite, respectively. The amount of CFX increased with increasing ionic strength, suggesting that both electrostatic and non-electrostatic interactions were important. After four reused time, CFX removal was greater than 66%, demonstrating that Tryp/gibbsite is reusable with high performance in removing CFX. The application in bacterial activity in term of E. coli reached greater than 98% that was the best material for bacteria inactivation. The present study reveals that Tryp/gibbsite is an excellent bio-material for removing CFX and E. coli.

Significance of MOF adsorbents in uranium remediation from water.

Uranium is considered as one of the most perilous radioactive contaminants in the aqueous environment. It has shown detrimental effects on both flora and fauna and because of its toxicities on human beings, therefore its exclusion from the aqueous environment is very essential. The utilization of metal-organic frameworks (MOFs) as an adsorbent for the removal of uranium from the aqueous environment could be a good approach. MOFs possess unique properties like high surface area, high porosity, adjustable pore size, etc. This makes them promising adsorbents for the removal of uranium from contaminated water. In this paper, sources of uranium in the water environment, human health disorders, and application of the different types of MOFs as well as the mechanisms of uranium removal have been discussed meticulously.

Removal of Acid Orange G Azo Dye by Polycation-Modified Alpha Alumina Nanoparticles.

Highly positively charged poly(vinyl benzyl trimethylammonium chloride) (PVBMA) was successfully synthesized with approximately 82% of yield. The PVBMA was characterized by the molecular weight (Mw ) of 343.45 g mol-1 and the molecular weight distribution, (D) of 2.4 by 1 H NMR and SEC measurements. The PVBMA was applied as an effective agent for α-Al2 O3 surface modification in the adsorptive removal of the azo dye acid orange G (AOG). The AOG removal performance was significantly enhanced at all pH compared to without surface modification. The experimental parameters were optimal at pH 8, free ionic strength, 15 min of adsorption time, and 5 mg mL-1 α-Al2 O3 adsorbents. The AOG adsorption which was mainly controlled by the PVBMA-AOG electrostatic attractions was better applicable to the Langmuir isotherm and the pseudo-second kinetic model. The PVBMA-modified α-Al2 O3 demonstrates a high-performance and highly reusable adsorbent with great AOG performances of approximately 90.1% after 6 reused cycles.

Adsorptive removal of dichlorophenoxyacetic acid (2,4-D) using novel nanoparticles based on cationic surfactant-coated titania nanoparticles.

A novel nanomaterial based on cationic surfactant-coated TiO2 nanoparticle (CCTN) was systematically fabricated in this work. Synthesized titania nanoparticles were thoroughly characterized by XRD, FT-IR, HR-TEM, TEM-EDX, SEM with EDX mapping, BET, and ζ potential measurements. The adsorption of cationic surfactant, cetyltrimethylammonium bromide (CTAB), on TiO2 was studied under various pH and ionic strength conditions. Adsorption of CTAB on TiO2 increased with ionic strength increment in the presence of hemimicelle monolayer structure, indicating that nonelectrostatic and electrostatic forces control CTAB uptake. CTAB adsorption isotherms on TiO2 were according to a two-step model. Potential application in pesticide removal of 2,4-dichorophenoxy acetic acid (2,4-D) using CCTN was also studied. Optimum parameters for 2,4-D treatment through adsorption technique were pH 5, adsorption time of 120 min, and CCTN dosage of 10 mg·mL-1. Very low 2,4-D removal efficiency using TiO2 without CTAB coating was found to be approximately 28.5% whereas the removal efficiency was up to about 90% by using CCTN under optimum conditions, and the maximum adsorption capacity of 12.79 mg·g-1 was found. Adsorption isotherms of 2,4-D on CCTN were more suitable with the Langmuir model than Freundlich. Adsorption mechanisms of 2,4-D on CCTN were mainly governed by Columbic attraction based on isotherms and surface charge changes.

Adsorption and transformation of tetracyclines on alpha alumina particles with surface modification by anionic surfactant.

The adsorption and transformation of tetracyclines (TCs) antibiotics, including oxytetracycline (OTC), chlortetracycline (CTC), and tetracycline (TC), on the sodium dodecyl sulfate (SDS) surfactant-modified α-Al2O3 particles were comprehensively investigated in this study. The TCs adsorption was significantly enhanced by using the modified adsorbents compared with the use of the unmodified adsorbents. The experimental conditions were systematically optimized and found to be pH 4, NaCl 1 mM, the contact time of 180 min, and the adsorbent dosage of 25 mg. mL-1. The high maximum adsorption capacities were approximately 320, 85, and 91 mg. g-1 for TC, OTC, and CTC, respectively. Meanwhile, the great removal efficiencies of the three antibiotics TC, OTC, and CTC were correspondingly 91.85, 88.4, and 98.3%. The TCs adsorption isotherm and kinetics on the SDS-modified α-Al2O3 particles mainly governed by the electrostatic and hydrophobic interactions were clarified by a suitable two-step model, the Fourier transform infrared spectroscopy (FT-IR) and zeta potential measurements. Meanwhile, the TCs structural transformation determined by the liquid chromatography with tandem mass spectrometry (LC-MS/MS) measurement was promoted through the adsorption on the α-Al2O3 surface. The TCs transformation rates strongly affected by the TCs adsorption were in the order of CTC > TC > OTC. The found results are promised that the SDS-modified α-Al2O3 particles might behave as high-performance adsorbents to remove the TCs from aqueous solutions.

Synthesis and Characterization of Novel Core-Shell ZnO@SiO2 Nanoparticles and Application in Antibiotic and Bacteria Removal.

A novel core-shell nanomaterial, ZnO@SiO2, based on rice husk for antibiotic and bacteria removal, was successfully fabricated. The ZnO@SiO2 nanoparticles were characterized by X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDX), Fourier transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), photoluminescence spectroscopy (PL), Brunauer-Emmett-Teller (BET) method, diffuse reflectance ultraviolet-vis (DR-UV-vis) spectroscopy, X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, and ζ-potential measurements. ß-Lactam antibiotic amoxicillin (AMX) was removed using ZnO@SiO2 nanoparticles with an efficiency greater than 90%, while Escherichia coli removal was higher than 91%. The optimum effective conditions for AMX removal using ZnO@SiO2, including solution pH, adsorption time, and ZnO@SiO2 dosage, were 8, 90 min, and 25 mg/mL, respectively. The maximum adsorption capacity reached 52.1 mg/g, much higher than those for other adsorbents. Adsorption isotherms of AMX on ZnO@SiO2 were more in accordance with the Freundlich model than the Langmuir model. The electrostatic attraction between negative species of AMX and the positively charged ZnO@SiO2 surface induced adsorption, while the removal of E. coli was governed by both electrostatic and hydrophobic interactions. Our study demonstrates that ZnO@SiO2 based on rice husk is a useful core-shell nanomaterial for antibiotic and bacteria removal from water.

Highly adsorptive protein inorganic nanohybrid of Moringa seeds protein and rice husk nanosilica for effective adsorption of pharmaceutical contaminants.

The present study aims to investigate adsorption characteristics and mechanisms of Moringa (MO) seeds protein on nanosilica rice husk and their applications in removal of pharmaceutical residues including the fluoroquinolone antibiotic levofloxacin (LFX) and the nonsteroidal anti-inflammatory drug diclofenac (DCF) in aquatic environment. Molecular weight of MO protein was determined by gel-permeation chromatography (GPC) method while its amino acids were quantified by high performance liquid chromatography (HPLC). The number-(Mn) and weight-average molecular weights (Mw) of MO protein were 1.53 × 104 and 1.61 × 104 g/mol, respectively. Different effective conditions on adsorption protein on nanosilica including contact time, pH, adsorbent dosage, and ionic strength were systematically optimized and found to be 180 min, 10, 10 mg/mL and 1 mM KCl, respectively. The surface charge change by zeta potential, surface modification by Fourier-transform infrared spectroscopy (FT-IR) and adsorption isotherms demonstrated that protein adsorption on nanosilica was governed by both electrostatic and non-electrostatic interactions. Application of protein functionalized nanosilica (ProFNS) in LFX and DCF removal were also thoroughly studied. The selected conditions for LFX and DCF removal using ProFNS were 1 mM KCl for both LFX and DCF; pH 8 and pH 6; contact time 90 and 120 min, and adsorption dosage 10 and 5 mg/ml for LFX and DCF, respectively. Adsorption isotherms of protein on nanosilica as well as LFX and DCF onto ProFNS at different ionic strengths were reasonably fitted by the two-step model while a pseudo-second-order model could fit adsorption kinetic well. The removal of LFX and DCF using ProFNS significantly increased from 51.51% to 87.35%, and 7.97%-50.02%, respectively. High adsorption capacities of 75.75 mg/g for LFX and 59.52 mg/g for DCF, indicate that ProFNS is a great performance for pharmaceutical residues removal in water environment.

pH- and Thermo-Responsive Water-Soluble Smart Polyion Complex (PIC) Vesicle with Polyampholyte Shells.

A diblock copolymer (P(VBTAC/NaSS)17-b-PAPTAC50; P(VS)17A50) composed of amphoteric random copolymer, poly(vinylbenzyl trimethylammonium chloride-co-sodium p-styrensunfonate) (P(VBTAC/NaSS); P(VS)) and cationic poly(3-(acrylamidopropyl) trimethylammonium chloride) (PAPTAC; A) block, and poly(acrylic acid) (PAAc49) were prepared via a reversible addition-fragmentation chain transfer radical polymerization. Scrips V, S, and A represent VBTAC, NaSS, and PAPTAC blocks, respectively. Water-soluble polyion complex (PIC) vesicles were formed by mixing P(VS)17A50 and PAAc49 in water under basic conditions through electrostatic interactions between the cationic PAPTAC block and PAAc49 with the deprotonated pendant carboxylate anions. The PIC vesicle collapsed under an acidic medium because the pendant carboxylate anions in PAAc49 were protonated to delete the anionic charges. The PIC vesicle comprises an ionic PAPTAC/PAAc membrane coated with amphoteric random copolymer P(VS)17 shells. The PIC vesicle showed upper critical solution temperature (UCST) behavior in aqueous solutions because of the P(VS)17 shells. The pH- and thermo-responsive behavior of the PIC vesicle were studied using 1H NMR, static and dynamic light scattering, and percent transmittance measurements. When the ratio of the oppositely charged polymers in PAPTAC/PAAc was equal, the size and light scattering intensity of the PIC vesicle reached maximum values. The hydrophilic guest molecules can be encapsulated into the PIC vesicle at the base medium and released under acidic conditions. It is expected that the PIC vesicles will be applied as a smart drug delivery system.

Removal of beta-lactam antibiotic in water environment by adsorption technique using cationic surfactant functionalized nanosilica rice husk.

This study aims to investigate the adsorption characteristics of cationic surfactant, cetyltrimethylamonium bromide (CTAB) onto negatively nanosilica rice husk surface and the application for antibiotic treatment in water environment. Adsorption of CTAB onto nanosilica increased with an increase of solution pH, due to an enhancement of the electrostatic attraction between cationic methylamomethylamonium groups and negatively charged nanosilica surface enhanced at higher pH. Adsorption of CTAB decreased with a decrease of ionic strength while a common intersection point (CIP) was observed for adsorption isotherm at different ionic strengths, suggesting that hydrophobic interactions between alkyl chains in CTAB molecules significantly induced adsorption and admicelles with bilayer formation were dominant than monolayer of hemimicelles. The CTAB functionalized nanosilica (CFNS) was applied for removal of beta-lactam amoxicillin (AMX). The best conditions for AMX treatment using CFNS were selected as pH 10, contact time 60 min and CFNS dosage 10 mg/mL. Removal efficiency of AMX using CFNS reached to 100% under optimum conditions while it was only 25.01% using nanosilica without CTAB. The maximum AMX adsorption capacity using CFNS of about 25 mg/g was much higher than other adsorbents. The effects of different organics such as humic acid, anionic surfactant, and other antibiotics on AMX removal using CFNS were also studied. A two-step model can fit CTAB uptake isotherms onto nanosilica and AMX onto CFNS well at different KCl concentrations. Based on the desorption of CTAB with AMX adsorption as well as adsorption isotherms, the change in surface charge and functional vibration groups after adsorption, we indicate that AMX adsorption onto CFNS was mainly controlled by electrostatic interaction. We reveal that CFNS is an excellent adsorbent for antibiotic treatment from aqueous solution.

Biochar Adsorbents for Arsenic Removal from Water Environment: A Review.

Arsenic intake can cause human health disorders to the lungs, urinary tract, kidney, liver, hyper-pigmentation, muscles, neurological and even cancer. Biochar is potent, economical and ecologically sound adsorbents for water purification. After surface modifications, adsorption capacity of biochar significantly increased due to high porosity and reactivity. Adsorption capacities of the biochar derived from the municipal solid waste and KOH mixed municipal solid waste were increased from 24.49 and 30.98 mg/g for arsenic adsorption. Complex formation, electrostatic behavior and ion exchange are important mechanisms for arsenic adsorption. Organic arsenic removal using biochar is a major challenge. Hence, more innovative research should be conducted to achieve one of the 17 sustainable development goals of the United Nations i.e. "providing safe drinking water for all". This review is focused on the arsenic removal from water using pristine and modified biochar adsorbents. Recent advances in production methods of biochar adsorbents and mechanisms of arsenic removal from water are also illustrated.

Synthesis, characterization of novel ZnO/CuO nanoparticles, and the applications in photocatalytic performance for rhodamine B dye degradation.

Photocatalytic deg radation of environmental pollutants is being up to date for the treatment of contaminated water. In the present study, ZnO/CuO nanomaterials were successfully fabricated by a simple sol-gel method and investigate the photo-degradation of rhodamine B (RhB). The synthesized ZnO/CuO nanoparticles were characterized by X-ray diffraction (XRD), energy-dispersive spectroscopy (EDS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV-Vis diffuse reflectance spectroscopy (UV-Vis-DRS), thermal analysis (TGA), surface charge, and Fourier transform infrared spectroscopy (FTIR). The photo-degradation of the dye RhB was followed spectroscopically. The overall composition of ZnO/CuO material was found to be wurtzite phase, with particle size of 30 nm, and the Vis light absorption increased with an increase of Cu content. The ZnO/CuO nanomaterials were highly active leading to a photo-degradation of 10 ppm RhB reaching 98% within 180 min at 0.1 g/L catalyst dosage. The change in surface charge after degradation evaluated by ζ potential measurements and the differences in functional vibration group monitored by Fourier transform infrared spectroscopy (FTIR) indicates that the RhB adsorption on the Zn45Cu surface was insignificant. And scavenging experiments demonstrate that the RhB degradation by ZnO/CuO nanomaterials involves to some degree hydroxyl radicals.

Adsorption of Binary Mixture of Highly Positively Charged PTMA5M and Partially Negatively Charged PAA onto PSL Particles Studied by Means of Brownian Motion Particle Tracking and Electrophoresis.

Effects of ionic strength on the adsorption of highly charged polycationic ((2-dimethylamino)ethyl methacrylate) methyl chloride quaternary salt (PTMA5M) individually as well as in a binary mixture with polyanionic acrylic acid (PAA) onto polystyrene sulfate latex (PSL) particles with negative charges were investigated by means of Brownian movement particle tracking and measurement of electrophoretic mobility. In addition, the adsorption mechanism was confirmed by Fourier transform infrared (FT-IR) and energy-dispersive X-ray (EDX) spectroscopic methods. The hydrodynamic thickness of the adsorbed polyelectrolyte layer (δH) and electrophoretic mobility (EPM) of particles as a function of concentration ratios of the two polyelectrolytes were measured to clarify the effect of negatively charged molecules on the structure of the positively charged adsorbed layer at various ionic strengths. Extremely thick δH was confirmed for the case of excess dosage of polycations. The δH decreased more significantly with the addition of PAA than increasing ionic strength. Interestingly, in the presence of PAA, the adsorbed layer thickness increased more at lower ionic strength than at higher ionic strength. In addition, the initial δH decreases remarkably after a time lapse of 1 h. Contrary to the decrease of the δH, almost all EPM either remained unchanged or increased over time depending on the concentration ratio of the two polyelectrolytes. Constant charge density, desorption of polyanions, and then reconformation of the adsorbed polycationic layer are proposed model components.

Temporal Changes of Adsorbed Layer Thickness and Electrophoresis of Polystyrene Sulfate Latex Particles after Long Incubation of Oppositely Charged Polyelectrolytes with Different Charge Densities.

The different desorption concepts of the two polyelectrolytes PTMA5M and PTMC5M, which have similar molecular weights and differ in the charge density on the polystyrene sulfate latex (PSL) particles by 25 times, and with various charge densities in a long incubation, were systematically investigated based on hydrodynamic adsorbed layer thickness (δH) and electrophoretic mobility (EPM) under two ionic strengths in the present study. Herein, in the case of highly charged polyelectrolyte PTMA5M, desorption continued for 4 h and re-adsorbing proceeded after a longer incubation time higher than 4 h. Meanwhile, in the case of lowly charged polyelectrolyte PTMC5M, an adsorption-desorption equilibrium was suggested to take into account the unchanging of both δH and EPM.

Adsorptive Removal of Anionic Azo Dye New Coccine Using Silica and Silica-gel with Surface Modification by Polycation.

In the present work, adsorption of anionic azo dye, new coccine (NCC) on silica and silica-gel in an aquatic environment was discovered. Effective conditions such as adsorption time, pH, the influence of dosage on NCC adsorption using strong polycation, poly-diallyl-dimethylammonium chloride (PDADMAC) modified silica (PMS) and PDADMAC modified silica-gel (PMSG) were systematically studied. The removal of NCC using PMS and PMSG were much higher than that using raw silica and silica-gel without PDADMAC in all pH ranges from 3 to 10. The adsorption of NCC onto PMS and PMSG was achieved maxima at the same conditions of contact time 30 min, pH 6. The optimum adsorbent dosages of PMS and PMSG for NCC removal were 10 and 20 mg·mL-1, respectively. Experimental results of NCC adsorption isotherms onto PMS and PMSG at different ionic strength were fitted by Langmuir and Freundlich models. The NCC removal efficiencies using PMS and PMSG were higher than 87%, indicating that PMS and PMSG are novel and reusable adsorbents for removal of anionic dye. Based on adsorption isotherms, and surface group changes after PDADMAC modification and NCC adsorption examined by Fourier transform infrared spectroscopy (FTIR), we demonstrate that electrostatic interaction between positively charged adsorbents' surfaces and negative sulfonic groups of NCC are the main driving force for anionic azo dye adsorption onto PMS and PMGS adsorbents.

Synthesis and Characterization of Novel Hybridized CeO2@SiO2 Nanoparticles Based on Rice Husk and Their Application in Antibiotic Removal.

This work aims to synthesize a core-shell material of CeO2@SiO2 based on rice husk as a novel hybridized adsorbent for antibiotic removal. The phase structures of CeO2@SiO2 and CeO2 nanoparticles that were fabricated by a simple procedure were examined by X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), and Fourier transform infrared (FT-IR) spectroscopy, while their interfacial characterizations were performed by scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), the Brunauer-Emmett-Teller (BET) method, and ζ-potential measurements. The removal efficiency of the antibiotic amoxicillin (AMX) using CeO2@SiO2 nanoparticles was much greater than that using SiO2 and CeO2 materials in solutions of different pH values. The optimum conditions for AMX removal using CeO2@SiO2 including contact time and adsorbent dosage were 120 min and 5 mg/mL, respectively. The maximum AMX removal using CeO2@SiO2 reached 100% and the adsorption capacity was 12.5 mg/g. Adsorption isotherms of AMX onto CeO2@SiO2 were fitted by Langmuir, Freundlich, and two-step adsorption models, while the adsorption kinetics of AMX achieved a better fit by the pseudo-second-order model than the pseudo-first-order model. The electrostatic and nonelectrostatic interactions between the zwitterionic form of AMX and the positively charged CeO2@SiO2 surface were controlled by adsorption. The effects of different organics such as humic acid, ionic surfactants, and pharmaceutical substances on AMX removal using CeO2@SiO2 were also thoroughly investigated. The high AMX removal efficiencies of about 75% after four regenerations and about 70% from an actual water sample demonstrate that CeO2@SiO2-based rice husk is a hybrid nanomaterial for antibiotic removal from water environments.

Esterification of sugarcane bagasse by citric acid for Pb2+ adsorption: effect of different chemical pretreatment methods.

In this study, different pretreatment strategies of sugarcane bagasse prior to citric acid modification were investigated in terms of Pb2+ adsorption capacity. Pretreatment strategies included the use of NaOH, HCl, and C2H5OH in various concentrations. In order to fundamentally understand how these pretreatment methods affect the modification of sugarcane bagasse by citric acid as well as the Pb2+ adsorption capacity of sugarcane bagasse, three main components of sugarcane bagasse namely cellulose, hemicellulose, and lignin were isolated and esterified by citric acid under the same conditions. ATR-FTIR, XPS, SEM, and an analysis of the number of carboxylic acid groups were used to investigate the physicochemical and chemical properties of the materials. These three components were proved to participate in adsorption and induce the esterification with citric acid. Hence, pretreatment with ethanol and 0.01 M NaOH which could retain cellulose, hemicellulose, and lignin in sugarcane bagasse achieved a high Pb2+ adsorption capacity, i.e., 122.4 and 97 mg/g after the esterification with citric acid. In contrast, pretreatment with 0.5 M NaOH and 0.1 M HCl removed lignin and hemicellulose, leading to the lowest value of approximately 45 mg/g for citric acid esterified-pretreated sugarcane bagasse. XPS analysis and number of carboxylic group measurement confirmed the esterification between bagasse and citric acid. To understand the adsorption mechanism of adsorbent, two kinetic models including pseudo-first-order model and pseudo-second-order model were applied. The experimental data were well described by the pseudo-second-order model. The adsorption isotherm data were fitted Langmuir and Freundlich.

Selective electrodialysis for simultaneous but separate phosphate and ammonium recovery.

Nutrients were extracted from digester supernatant sampled from a full-scale enhanced biological phosphorus removal (EBPR) wastewater treatment plant. A four-compartment selectrodialysis setup was used to extract ammonium and phosphate in two separate compartments. The initial phosphate recovery rate was measured to be 0.072 mmol m-2 s-1 and the initial ammonium recovery rate was measured to be 1.31 mmol m-2 s-1. The ammonium recovery rate was 18 times higher than that for phosphate, whereas the molar concentration of ammonium in the feed was 10 times higher than that of phosphate. An average recovery of 72 ± 1% and 90 ± 10% for ammonium and phosphate was observed after 3 h of operation. A monovalent anion selective (MVA) membrane was used to avoid ammonium and reduce the concentration of monovalent anions in the phosphorus stream. The pH in the phosphorus stream was kept at 10 so phosphate did not pass the MVA membrane. A membrane area of 26 m2 per m3 digester supernatant was required to recover 70% of phosphate and ammonium for the digester supernatant that contained 6 mM phosphate and 105 mM ammonium.

COVID-19 impacts of inbound tourism on Australian economy.

The pandemic COVID-19 has severely impacted upon the world economy, devastating the tourism industry globally. This paper estimates the short-run economic impacts of the inbound tourism industry on the Australian economy during the pandemic. The analysis covers effects both at the macroeconomic as well as at the industry and occupation level, from direct contribution (using tourism satellite accounts) to economy-wide effects (using the computable general equilibrium modelling technique). Findings show that the pandemic affects a range of industries and occupations that are beyond the tourism sector. The paper calls for strong support from the government on tourism as the recovery of tourism can deliver spillover benefits for other sectors and across the whole spectrum of occupations in the labour market.

Separation and determination of alkyl sulfate surfactants in wastewater by capillary electrophoresis coupled with contactless conductivity detection after preconcentration by simultaneous adsorption using alumina beads.

The aim of the present study is to determine four anionic alkyl sulfate (AS) surfactants with different alkyl chains, namely, C8, C10, C12, and C14, in wastewater by CE with capacitively coupled contactless conductivity detection (CE-C4 D). The conditions effective for the separation of the four AS surfactants were systematically optimized and found to be in a Tris-His (50 mM/20 mM) BGE solution at a pH of 8.95, using a separation voltage of +15 kV, hydrodynamic injection by siphoning using a 20 cm injection height and an injection time of 20 s. The LODs for C8, C10, C12, and C14 were 2.58, 2.30, 2.08, and 3.16 mg/L, respectively. The conditions used to achieve the simultaneous adsorption and preconcentration of the AS surfactants using Al2 O3 beads were pH of 3 and 0.1 mM NaCl. The adsorption efficiencies were found to be 45.6, 50.8, 81.7, and 99.9%, while the desorption efficiencies reached 66.1, 70.4, 83.9, and 100.0% for C8, C10, C12, and C14, respectively. The concentrations of the AS surfactants in wastewater samples were quantified by CE-C4 D after preconcentration by simultaneous adsorption using Al2 O3 beads. The results obtained from the proposed method were consistent with those obtained by HPLC-MS/MS, with a deviation of less than 15%. Our results indicate that the CE-C4 D performed after preconcentration by an adsorption technique using Al2 O3 beads is a new, inexpensive, and suitable method for quantifying AS surfactants in wastewater samples.