Characterization and Performance of Peanut Shells in Caffeine and Triclosan Removal in Batch and Fixed-Bed Column Tests.

Peanut shells' adsorption performance in caffeine and triclosan removal was studied. Peanut shells were analyzed for their chemical composition, morphology, and surface functional groups. Batch adsorption and fixed-bed column experiments were carried out with solutions containing 30 mg/L of caffeine and triclosan. The parameters examined included peanut shell particle size (120-150, 300-600, and 800-2000 µm), adsorbent dose (0.02-60 g/L), contact time (up to 180 min), bed height (4-8 cm), and hydraulic loading rate (2.0 and 4.0 m3/m2-day). After determining the optimal adsorption conditions, kinetics, isotherm, and breakthrough curve models were applied to analyze the experimental data. Peanut shells showed an irregular surface and consisted mainly of polysaccharides (around 70% lignin, cellulose, and hemicellulose), with a specific surface area of 1.7 m2/g and a pore volume of 0.005 cm3/g. The highest removal efficiencies for caffeine (85.6 ± 1.4%) and triclosan (89.3 ± 1.5%) were achieved using the smallest particles and 10.0 and 0.1 g/L doses over 180 and 45 min, respectively. Triclosan showed easier removal compared to caffeine due to its higher lipophilic character. The pseudo-second-order kinetics model provided the best fit with the experimental data, suggesting a chemisorption process between caffeine/triclosan and the adsorbent. Equilibrium data were well-described by the Sips model, with maximum adsorption capacities of 3.3 mg/g and 289.3 mg/g for caffeine and triclosan, respectively. In fixed-bed column adsorption tests, particle size significantly influenced efficiency and hydraulic behavior, with 120-150 µm particles exhibiting the highest adsorption capacity for caffeine (0.72 mg/g) and triclosan (143.44 mg/g), albeit with clogging issues. The experimental data also showed good agreement with the Bohart-Adams, Thomas, and Yoon-Nelson models. Therefore, the findings of this study highlight not only the effective capability of peanut shells to remove caffeine and triclosan but also their versatility as a promising option for water treatment and sanitation applications in different contexts.

Electronic Tongue Coupled to an Electrochemical Flow Reactor for Emerging Organic Contaminants Real Time Monitoring.

Triclosan, which is a bacteriostatic used in household items, has raised health concerns, because it might lead to antimicrobial resistance and endocrine disorders in organisms. The detection, identification, and monitoring of triclosan and its by-products (methyl triclosan, 2,4-Dichlorophenol and 2,4,6-Trichlorophenol) are a growing need in order to update current water treatments and enable the continuous supervision of the contamination plume. This work presents a customized electronic tongue prototype coupled to an electrochemical flow reactor, which aims to access the monitoring of triclosan and its derivative by-products in a real secondary effluent. An electronic tongue device, based on impedance measurements and polyethylenimine/poly(sodium 4-styrenesulfonate) layer-by-layer and TiO2, ZnO and TiO2/ZnO sputtering thin films, was developed and tested to track analyte degradation and allow for analyte detection and semi-quantification. A degradation pathway trend was observable by means of principal component analysis, being the sample separation, according to sampling time, explained by 77% the total variance in the first two components. A semi-quantitative electronic tongue was attained for triclosan and methyl-triclosan. For 2,4-Dichlorophenol and 2,4,6-Trichlorophenol, the best results were achieved with only a single sensor. Finally, working as multi-analyte quantification devices, the electronic tongues could provide information regarding the degradation kinetic and concentrations ranges in a dynamic removal treatment.

Fate of triclosan in laboratory-scale activated sludge reactors - Effect of culture acclimation.

Triclosan (TCS); a widely used antimicrobial biocide, exists in several pharmaceutical and personal care products. Due to its wide usage, TCS is detected in wastewater at varying concentrations. Biological treatability of TCS and its effect on chemical oxygen demand (COD) removal efficiency were investigated running laboratory-scale pulse-fed sequencing batch reactors with acclimated and non-acclimated cultures. The culture was acclimatized to TCS by gradually increasing its concentration in the synthetic feed wastewater from 100 ng/L to 100 mg/L. There were no effects of TCS on COD removal efficiency up to the TCS concentration of 500 ng/L for both acclimatized and non-acclimatized cases. However, starting from a concentration of 1 mg/L, TCS affected the COD removal efficiency adversely. This effect was more pronounced with non-acclimatized culture. The decrease in the COD removal efficiency reached to 47% and 42% at the TCS concentration of 100 mg/L, under acclimation and non-acclimation conditions respectively. Adsorption of TCS into biomass was evidenced at higher TCS concentrations especially with non-acclimated cultures. 2,4-dichlorophenol and 2,4-dichloroanisole were identified as biodegradation by-products. The occurrence and distribution of these metabolites in the effluent and sludge matrices were found to be highly variable depending, especially, on the culture acclimation conditions.

Ionic liquid assisted electrospun cellulose acetate fibers for aqueous removal of triclosan.

The cellulose acetate (CA) membrane prepared via electrospun was innovatively utilized as fiber-adsorbent for the separation of aqueous triclson (TCS). It was found that the presence of the room temperature ionic liquid (RTIL) in the precursor amplified electric force toward the CA-solution, thereby benefiting the formation of CA fibers. The as-spun CA fibers exhibit excellent adsorptive performance toward TCS, with fast adsorption kinetics, and the maximum adsorption capacity achieved to 797.7 mg g(-1), which established much better performance in contrast to conventional adsorbents. We proposed that the adsorption of TCS onto CA fibers was primarily facilitated by the hydrogen bonding between the abundant carbonyl, hydroxyl groups of CA surface, and the hydrogen atoms of phenol functional groups in TCS molecular.

Facile fabrication of magnetic carbon composites from hydrochar via simultaneous activation and magnetization for triclosan adsorption.

Advanced magnetic carbon composites with high specific surface area and high microporosity are required for both environmentally and agriculturally related applications. However, more research is needed for the development of a facile and highly efficient synthesis process. In the present work, a novel approach of simultaneous activation and magnetization is proposed for the fabrication of magnetic carbon composites via the thermal pyrolysis of hydrochar (i.e., a solid residue from a hydrothermal carbonization process) that has been pretreated with mixtures of ferric chloride (FeCl3) and zinc chloride (ZnCl2). The main objective of this study is the investigation of the variation of characteristics of magnetic carbon composites produced at various conditions, as well as triclosan (TCS) adsorption behavior on such composites. This presented simple one-step synthesis method has the following advantages: (a) the hydrochar is activated with high surface area and pore volume (up to 1351 m(2)/g and 0.549 cm(3)/g, respectively), (b) activation and magnetization are simultaneously achieved without further modification, (c) the magnetic particles (γ-Fe2O3) are stable under an acidic medium (pH of 3.0 and 4.0), and (d) the products have the potential to remove TCS from aqueous solutions with a maximum adsorption capacity of 892.9 mg/g. The results indicate the effectiveness of this facile synthesis strategy in converting low-value biowaste into a functional material with high performance for pollutant removal from aqueous solutions.

Transformation products and human metabolites of triclocarban and triclosan in sewage sludge across the United States.

Removal of triclocarban (TCC) and triclosan (TCS) from wastewater is a function of adsorption, abiotic degradation, and microbial mineralization or transformation, reactions that are not currently controlled or optimized in the pollution control infrastructure of standard wastewater treatment. Here, we report on the levels of eight transformation products, human metabolites, and manufacturing byproducts of TCC and TCS in raw and treated sewage sludge. Two sample sets were studied: samples collected once from 14 wastewater treatment plants (WWTPs) representing nine states, and multiple samples collected from one WWTP monitored for 12 months. Time-course analysis of significant mass fluxes (α=0.01) indicate that transformation of TCC (dechlorination) and TCS (methylation) occurred during sewage conveyance and treatment. Strong linear correlations were found between TCC and the human metabolite 2'-hydroxy-TCC (r=0.84), and between the TCC-dechlorination products dichlorocarbanilide (DCC) and monochlorocarbanilide (r=0.99). Mass ratios of DCC-to-TCC and of methyl-triclosan (MeTCS)-to-TCS, serving as indicators of transformation activity, revealed that transformation was widespread under different treatment regimes across the WWTPs sampled, though the degree of transformation varied significantly among study sites (α=0.01). The analysis of sludge sampled before and after different unit operation steps (i.e., anaerobic digestion, sludge heat treatment, and sludge drying) yielded insights into the extent and location of TCC and TCS transformation. Results showed anaerobic digestion to be important for MeTCS transformation (37-74%), whereas its contribution to partial TCC dechlorination was limited (0.4-2.1%). This longitudinal and nationwide survey is the first to report the occurrence of transformation products, human metabolites, and manufacturing byproducts of TCC and TCS in sewage sludge.

Rotating disk sorptive extraction of triclosan and methyl-triclosan from water samples.

A method of sample preparation based on use of rotating disk sorptive extraction (RDSE) has been developed for determination of triclosan (TCS) and methyl-triclosan (MTCS) in water samples. The sorptive and desorptive behavior of the analytes was studied by use of a rotating disk coated with polydimethylsiloxane (PDMS) on one of its surfaces. Chemical and extraction behavior were studied to establish the best conditions for extraction. The optimum conditions for both analytes were: sample volume 25 mL, pH 4.5, NaCl concentration 6% (w/v), disk rotational velocity 1,250 rpm, and extraction time 80 min. A desorption time of 30 min was used with 5 mL methanol. The detection limits for TCS and MTCS were 46 and 34 ng L(-1), respectively. Recovery was evaluated at two concentrations, 160 and 800 ng L(-1), and the values obtained were between 80 and 100%. The method was applied to analysis of influent water at two treatment plants in Santiago, Chile.

Effect of wastewater chlorination on endocrine disruptor removal.

Endocrine disrupting chemicals (EDCs) are compounds of mainly anthropogenic origin that interfere with the endocrine system of animals and humans thus causing a series of disorders. Wastewater treatment plants are one of the major routes for transporting such chemicals to the water courses. In the context of this study, several chlorination batch tests were performed in order to assess the effectiveness of chlorination to remove bisphenol A (BPA), triclosan (TCS), nonylphenol (NP) and its ethoxylates (NP1EO and NP2EO) from secondary effluent. According to the results, an appreciable removal of NP, BPA and TCS to the order of 60-84% was observed as an effect of moderate chlorination doses. This was not the case for NP1EO and NP2EO as even at high chlorine doses, removal efficiencies were lower (37% for NP1EO and 52% for NP2EO). Removal efficiencies of NP, BPA and TCS are practically independent of contact time, although this was not the case for NP1EO and NP2EO. Based on toxicity experiments, it is anticipated that following chlorination of the target chemicals, production of more toxic metabolites is taking place. Therefore the effectiveness of chlorination to remove EDCs is questionable and more research is needed to guarantee safe wastewater reuse.

Analysis of wastewater samples by direct combination of thin-film microextraction and desorption electrospray ionization mass spectrometry.

An analysis method for aqueous samples by the direct combination of C18/SCX mixed mode thin-film microextraction (TFME) and desorption electrospray ionization mass spectrometry (DESI-MS) was developed. Both techniques make analytical workflow simpler and faster, hence the combination of the two techniques enables considerably shorter analysis time compared to the traditional liquid chromatography mass spectrometry (LC-MS) approach. The method was characterized using carbamazepine and triclosan as typical examples for pharmaceuticals and personal care product (PPCP) components which draw increasing attention as wastewater-derived environmental contaminants. Both model compounds were successfully detected in real wastewater samples and their concentrations determined using external calibration with isotope labeled standards. Effects of temperature, agitation, sample volume, and exposure time were investigated in the case of spiked aqueous samples. Results were compared to those of parallel HPLC-MS determinations and good agreement was found through a three orders of magnitude wide concentration range. Serious matrix effects were observed in treated wastewater, but lower limits of detection were still found to be in the low ng L(-1) range. Using an Orbitrap mass spectrometer, the technique was found to be ideal for screening purposes and led to the detection of various different PPCP components in wastewater treatment plant effluents, including beta-blockers, nonsteroidal anti-inflammatory drugs, and UV filters.

Miniaturized extraction methods of triclosan from aqueous and fish roe samples. Bioconcentration studies in zebrafish larvae (Danio rerio).

Triclosan, an antibacterial and antifungal agent, is widely used in household and personal care products, processed foods and food packaging, etc., and thus also released into the environment. Triclosan is acutely and chronically toxic to aquatic organisms and bioaccumulates in fish tissue. Here, we propose a new miniaturized triclosan extraction method for aqueous and fish roe samples, based on the use of a vortex mixer and an ultrasonic probe, respectively, and useful for triclosan determination by gas chromatography coupled to a micro electron capture detector. Different solvents for extraction and sorbents for clean-up purposes were tested. Multivariate optimization of the variables affecting ultrasonic extraction (ultrasound radiation amplitude, sonication time, sample temperature, and the ratio of sample amount and extracting volume) was carried out. Solvent extraction using ethyl acetate and further clean-up with mixed bed cartridges with two layers of Florisil® and Florisil® impregnated with 10% sulfuric acid only for fish roe samples was finally selected. Extraction efficiencies of up to 95% and 90%, and detection limits of 0.165 ng ml(-1) and 2.7 ng g(-1) for aqueous and fish roe samples were obtained, respectively. The optimized method was used in bioconcentration studies with zebrafish larvae (Danio rerio), as an alternative method to the Organization for Economic Cooperation and Development technical guideline 305. Bioconcentration values, BCF = 2,630 and 2,018 at exposure concentrations of 30 and 3 µg L(-1), respectively, were assessed. These results are in agreement with those reported in the literature, showing the feasibility of the method for estimation of toxicokinetic parameters and bioconcentration factors using zebrafish larvae instead of adult fishes, reducing considerable animal testing, as suggested by the European legislation.

Simultaneous determination of triclosan, triclocarban, and transformation products of triclocarban in aqueous samples using solid-phase micro-extraction-HPLC-MS/MS.

The presence of triclosan and triclocarban, two endocrine-disrupting chemicals and antimicrobial agents, and transformation products of triclocarban, 1,3-di(phenyl)urea, 1,3-bis(4-chlorophenyl)urea and 1,3-bis(3,4-dichlorophenyl)urea, in tap water, treated household drinking water, bottled water, and river water samples were investigated using solid-phase micro-extraction coupled with-HPLC-MS/MS, a rapid, green, and sensitive method. Factors influencing the quantity of the analytes extracted onto the solid-phase micro-extraction fiber, such as addition of salt, sample pH, extraction time, desorption time, and sample volume, were optimized using solid-phase micro-extraction-HPLC-MS/MS. The results showed that the method gave satisfactory sensitivities and precisions for analyzing sub-part-per-trillion levels of triclosan, triclocarban, and transformation products of triclocarban in samples collected locally. The recoveries of analytes ranged from 97 to 107% for deionized water samples, and 99 to 110% for river water samples, and limits of detection were in the range of 0.32-3.44 and 0.38-4.67 ng/L for deionized water and river water samples, respectively. On average, the daily consumption of triclosan and triclocarban by an adult by consuming 2 liters of different types of drinking water were estimated to be in the range of 6.13-425 ng/day as a result of the concentrations of triclosan and triclocarban measured in this study.

Determination of trace triclosan in environmental water by microporous bamboo-activated charcoal solid-phase extraction combined with HPLC-ESI-MS.

A sensitive and efficient analytical method for triclosan (TCS) determination in water, which involves enrichment with bamboo-activated charcoal and detection with HPLC-ESI-MS, was developed. The influence of several operational parameters, including the eluant and its volume, the flow rate, the volume andacidity of the sample, and the amount of bamboo-activated charcoal, were investigated and optimized. Under the optimum conditions, linearity of the method was observed in the range of 0.02-20 µg/L, with correlation coefficients (r(2) ) >0.9990. The limit of detection was 0.002 µg/L based on the ratio of chromatographic signal to baseline noise (S/N = 3). The spiked recoveries of TCS in real water samples were achieved in the range of 97.6-112.5%. The proposed method was applied to analyze TCS in real aqueous samples. All the surface water samples collected in Xiaoqing River had detectable levels of TCS with concentrations of 42-197 ng/L.

Triclosan: its occurrence, fate and effects in the Australian environment.

Triclosan (TCS) is an antimicrobial agent used widely in household products such as soaps, household cleaners, cosmetics, sportswear, mouthwash and toothpaste. It is a bioaccumulative compound known for its high toxicity to algae, daphnids, fish and other aquatic organisms. We investigated its occurrence in effluents, biosolids and surface waters in Australia, as well as its fate in Australian soils and wastewater treatment plants (WWTPs), including the effects on microbial processes in soils. The concentrations of TCS in 19 effluents ranged from 23 to 434 ng/L (median 108 ng/L) and in 17 biosolids from 0.09 to 16.79 mg/kg on dry weight basis (median 2.32 mg/kg). TCS at concentrations of up to 75 ng/L were detected in receiving waters from five creeks affected by effluent discharge from WWTPs. The removal rate of TCS in five selected WWTPs ranged from 72 and 93%, ascribed mainly to sorption onto sludge and biological degradation. Biodegradation in a clay loam soil was noted with a half life of 18 days. However the half-lives under field conditions are expected to be very different. The studies on the effect of TCS on soil microbiological processes showed that triclosan can disrupt the nitrogen cyclein sensitive soils at concentrations ≥5 mg/kg. In view of the recent risk assessment by the Australian regulatory agency NICNAS, there is an urgent need to assess exposure to TCS and its effect on ecosystem health.

In-sample acetylation-non-porous membrane-assisted liquid-liquid extraction for the determination of parabens and triclosan in water samples.

A procedure for the determination of seven parabens (esters of 4-hydroxybenzoic acid), including the distinction between branched and linear isomers of propyl- and butyl-parabens and triclosan in water samples, was developed and evaluated. The procedure includes in-sample acetylation-non-porous membrane-assisted liquid-liquid extraction and large volume injection-gas chromatography-ion trap-tandem mass spectrometry. Different derivatisation strategies were considered, i.e. post-extraction silylation with N-methyl-N-(tert-butyldimethylsilyl)-trifluoroacetamide and in situ acylation with acetic anhydride (Ac(2)O) and isobutylchloroformate. Moreover, acceptor solvent and the basic catalyser of the acylation reaction were investigated. Thus, in situ derivatisation with Ac(2)O and potassium hydrogenphosphate (as basic catalyser) was selected. Potassium hydrogenphosphate overcomes some drawbacks of other basic catalysers, e.g. toxicity and bubble formation, while leads to higher responses. Subsequently, other experimental variables affecting derivatisation-extraction yield such as pre-stirring time, salt addition and volume of Ac(2)O were optimised by an experimental design approach. Under optimised conditions, the proposed method achieved detection limits from 0.1 to 1.4 ng L(-1) for a sample volume of 18 mL and extraction efficiencies, estimated by comparison with liquid-liquid extraction, between 46% (for methyl- and ethyl-parabens) and 110% (for benzylparaben). The reported sample preparation approach is free of matrix effects for parabens but affected for triclosan with a reduction of approximately 40% when wastewater samples are analysed; therefore, both internal and external calibration can be used as quantification techniques for parabens, but internal standard calibration is mandatory for triclosan. The application of the method to real samples revealed the presence of these compounds in raw wastewater at concentrations up to 26 ng mL(-1), the prevalence of the linear isomer of propylparaben (n-PrP), and the coexistence of the two isomers of butylparaben (i-BuP and n-BuP) at similar levels.

Removal of triclosan during wastewater treatment process and sewage sludge composting-A case study in the middle reaches of the Yellow River.

Triclosan (TCS) is widely used as an antibacterial disinfectant in personal care products, especially in rapidly-urbanizing countries, such as China. Almost all TCS enters wastewater treatment plants (WWTPs), but the fate of the TCS in the WWTPs is unclear. TCS may be present in sewage sludge or in effluent, and the discharge of TCS into an ecosystem can pose environmental risks. In the present study, influent, effluent, and sewage sludge were collected from four typical urban WWTPs, and the fate of TCS in the plants was investigated. The study was conducted in Zhengzhou, a city in the middle reaches of the Yellow River in China. The sewage sludge was used for aerobic composting to study the influences of different ventilation treatments on the biodegradation effects of TCS and the changes in the microbial community during the composting process. The results showed that the mean concentration of TCS in the influent of the four typical WWTPs was 397.1 ng/L. The mean level of TCS in the effluent was 8.0 ng/L. The mean concentration of TCS in the sewage sludge was 814.4 ng/g. For the four WWTPs, the percentages of TCS removal were 97.6% (Nansanhuan), 97.6% (Xinzheng), 98.8% (Wulongkou), and 97.9% (Chenyu), respectively. The sewage sludge enrichment rates for TCS ranged between 36.4% and 49%. Therefore, there is a need to focus on the environmental risks from sewage sludge. During aerobic composting, the TCS was effectively degraded under three ventilation strategies. Thus, improved ventilation could enhance the degradation rate of TCS. Moreover, TCS degradation occurred in the mesophilic period and in the early stage of the thermophilic phase period. Finally, the degradation rates of TCS in sewage sludge samples composted with low-, medium-, and high-ventilation treatments were 48.1%, 59.0%, and 59.5%, respectively. Thus, high ventilation could provide enough oxygen for the pile and enhanced microorganism activity, benefiting the degradation of TCS. In addition, the microbial communities change during the composting process, and a diversity index of the changes can help explain the composting process.

Removal of organic micropollutants from biologically treated greywater using continuous-flow vacuum-UV/UVC photo-reactor.

Despite growing apprehension regarding the fate of organic micropollutants (MPs) of emerging concern, little attention has been paid to their presence in domestic greywater, where they mainly originate from personal care products. Many MPs are not fully removed in conventional greywater treatments and require additional treatment. Vacuum-UV radiation (VUV) can generate ·OH in situ, via water photolysis, initiating advanced oxidation process (AOP) without any chemical addition. Despite growing interest in VUV-based AOP, its performance in real-life grey- or wastewater matrices has hardly been investigated. The present study investigates the removal of triclosan (TCS) and oxybenzone (BP3), common antibacterial and UV-filter MPs, in deionized water (DIW) and in treated greywater (TGW) using combined UVC/VUV or UVC only radiation in a continuous-flow reactor. Degradation kinetics of these MPs and their transformation products (TPs) were addressed, as well as bacterial growth inhibition of the resulting reactor's effluent. In DIW, MP degradation was much faster under the combined UVC/VUV irradiation. In TGW, the combined radiation successfully removed both MPs but at lower efficiency than in DIW, as particles and dissolved organic matter (DOM) acted as radical scavengers. Filtration and partial DOM removal prior to irradiation improved the process efficiency and reduced energy requirements under the combined radiation (from 1.6 and 167 to 1.1 and 6.0 kWh m-3·Ö¼order-1 for TCS and BP3, respectively). VUV radiation also reduced TP concentrations in the effluent. As a result, bacterial growth inhibition of triclosan solution irradiated by VUC/VUV was lower than that irradiated by UVC light alone, for UV dose > 120 mJ cm-2.

A novel strategy for selective removal and rapid collection of triclosan from aquatic environment using magnetic molecularly imprinted nano-polymers.

Triclosan (TCS) is a kind of chronic toxicity to aquatic organisms. Due to its highly effective antimicrobial, TCS has been widely applied in personal-care products, which naturally poses a potential risk to the ecological system and human health since its release into water-ecological environment. Therefore, it urgently demands a selective, easily separated, recyclable, and low-cost adsorbent to remove the residues of TCS from aquatic environments. In this study, a novel magnetic molecularly imprinted nano-polymers (TMIPs) were prepared for selective adsorption and convenient collection of TCS in aquatic samples, based on a core-shell technique using TCS as template molecule and SiO2-coated Fe3O4 nanoparticles as the support substrate. The functional groups, particle size, morphology and magnetic property of TMIPs were characterized by Fourier-transform infrared spectroscopy, scanning electron microscope, transmission electron microscopy and vibrating sample magnetometer, respectively. The obtained TMIPs possessed excellent adsorption capacity (Qe = 53.12 mg g-1), speedy adsorption equilibrium time (2 min) and high selectivity (k' = 6.321) for TCS. Moreover, the pH-tolerance and stability tests manifested that the adsorption capacity of TMIPs for TCS was acid-resistance and could retain 94.2% of the maximum Qe after 5 times removal-regeneration cycles. The feature of magnetically susceptibility can simplify the procedures of sample handling in TCS determination, because the TMIPs of TCS are easy to be recycled from aquatic samples. As an application demonstration, the toxicity test in microalgae confirmed that a tiny amount of TMIPs could significantly eliminate the toxic effect of TCS on Chlamydomonas reinhardtii via the efficient binding with TCS.

Eco-friendly rapid removal of triclosan from seawater using biomass of a microalgal species: Kinetic and equilibrium studies.

Triclosan is an important emerging pollutant. It has become ubiquitous due to its incomplete elimination in municipal wastewater treatment plants causing serious environmental problems. Biomass from microorganisms as sorbent of pollutants can be an eco-friendly alternative for triclosan removal. In this work, the elimination of triclosan using biomass (dead and living) of the marine microalga Phaeodactylum tricornutum was characterized in cultures exposed to light and in a complex solution (seawater). Maximum removal capacity, isotherms, kinetics, FTIR characterization, pH effect and reuse were evaluated and discussed. Photodegradation of triclosan was also evaluated. Both biomasses showed similar effectiveness; around 100% of pollutant was eliminated when its concentration was 1 mg L-1 in only 3 h using a biomass concentration of 0.4 g L-1. A pseudo-second order model guided the biosorption process. Considering the photodegradation as a first-order process, the whole process (photodegradation + biosorption) was suitably modelled with pseudo-third order and Elovich kinetics. Biosorption increased with the decrease in pH. Temkin isotherm showed the best fit for the experimental data. Both biomasses showed good reuse after five cycles, losing only 7% in efficiency. P. tricornutum biomass is an attractive eco-material for triclosan elimination with low-cost and easy handling than other sorbents.

Biomimetic lipophilic activated carbon for enhanced removal of triclosan from water.

Triclosan, an antimicrobial micro-pollutant with a high bio-accumulation potential represented by its high octanol-water partition coefficient (log Kow) of 4.76 is commonly encountered in water and wastewater worldwide. The present study focuses on biomimetic surface modification of commercial activated carbon (PAC) with long chain fatty acid namely docosahexaenoic acid (DHA) resulting in enhanced affinity for the hydrophobic micro-pollutant; triclosan (TCS). The sorption process of the resulting modified lipophilic carbon (PACM) was investigated for the effect of various experimental conditions. The Freundlich isotherm and pseudo-second-order kinetic models had a better fit. PACM exhibited the maximum adsorption capacity of 395.2 mg g-1 in contrast to 71.5 mg g-1 obtained for PAC. The surface morphology in terms of surface area, surface acidity, pore size, contact angle, etc. and were also evaluated. The contact angle of 134.3° obtained for PACM confirmed its highly hydrophobic nature. The efficacy of PACM was also evaluated using real-world secondary treated effluent containing triclosan confirming its applicability for tertiary treatment of wastewater. The study established that the biomimetic approach of creating lipid-like sites on the carbon surface results in the enhanced removal of lipophilic micro-pollutants. It can also be utilized for the removal and recovery of a wide variety of other organic micro-pollutants.

Occurrence and removal of triclosan in Canadian wastewater systems.

Triclosan (TCS) is an antimicrobial agent used in many personal care and cleaning products. It has been detected in most environmental compartments and the main entry pathway is wastewater effluents and biosolids. TCS was analyzed in 300 samples of raw influent, final effluent, and biosolids from 13 wastewater treatment plants (WWTPs) across Canada representing five types of typical wastewater treatment systems. TCS was almost always detected in influent (median 1480 ng/L), effluent (median 107 ng/L), and biosolids (median 8000 ng/g dry weight) samples. Removals of TCS from lagoons as well as secondary and advanced treatment facilities were significantly higher than primary treatment facilities (p < 0.001). TCS removal was strongly correlated with organic nitrogen removal. TCS removals at most lagoons and plants that use biological treatment were higher during summer compared with winter. However, no seasonal or temperature effects were observed at the two primary facilities, likely due to the absence of biological activity. Aerobically digested solids contained the lowest levels (median 555 ng/g) while anaerobically digested primary solids contained the highest levels of TCS (median 22,700 ng/g). The results of this large comprehensive study demonstrate that TCS is consistently present in wastewater and biosolids at relatively high concentrations and that removal from wastewater and levels in biosolids are strongly influenced by the wastewater and solids treatment types.