A polythiophene/UiO-66 composite coating for extraction of volatile organic compounds migrated from ion-exchange resins prior to their determination by gas chromatography.

A Poly (3,4-ethylenedioxothiophene) (PEDOT)/UiO-66 composite was electrodeposited on an etched stainless-steel wire as head-space solid-phase microextraction (HS-SPME) coating. A robust, well controlled thickness, and uniform coating of metal organic framework composites can be realized by the electrodeposited strategy. The incorporated UiO-66 not only enhanced the uniformity and stability of the composite coating, but also effectively decreased the stacking phenomenon of PEDOT and improved its extraction efficiency, which was over 100 times higher than that of the PEDOT coating without UiO-66. The composite coating was used to enrich seven types of volatile organic compounds (VOCs) in ion-exchange resins, including methyl cyclohexane, benzene, toluene, ortho-xylene, styrene, para-xylene and divinyl-benzene. The results of adsorption isotherm analysis showed that π stacking effect played dominant role between the composite coating and VOCs in the extraction process. The composite coating was characterized by scanning electron microscopy, X-ray diffraction, Fourier transform infrared and thermogravimetric analysis, respectively. A determination method for seven kinds of VOCs was established by HS-SPME coupled with gas chromatography-flame ionization detection (GC-FID). Under the optimal experimental conditions, the detection linear range (LRs) was 0.09-100 ng mL-1, and the detection limit (LODs) was 0.03-0.06 ng mL-1 (S/N = 3). The method was applied for the migration detection of VOCs in four types of ion-exchange resin, which showed satisfactory recovery (84.5-117.2%).

Deep eutectic solvent functionalized graphene oxide composite adsorbent for miniaturized pipette-tip solid-phase extraction of toluene and xylene exposure biomarkers in urine prior to their determination with HPLC-UV.

A deep eutectic solvent functionalized graphene oxide composite adsorbent (DFG) was synthesized through reversible-addition fragmentation chain-transfer polymerization. The synthesized DFG had multiple adsorption interactions after covalent modification with a deep eutectic solvent (allyltriethylammonium bromide/ethylene glycol). Adsorption isotherms and kinetics studies of DFG indicate that the adsorption of hippuric acid (HA) and methylhippuric acid (MHA) was monolayer chemical adsorption. The comparison of DFG with commercial adsorbents demonstrates that the adsorption ability of DFG was superior. This was due to the multiple adsorption interactions of DFG for the three analytes (mainly π-interaction, hydrogen bonding, electrostatic adsorption, and hydrophobic interaction). The DFG adsorbent was applied to miniaturized pipette-tip solid-phase extraction (MPT-SPE), followed by high-performance liquid chromatography (HPLC) to determine biomarkers in urine for toluene and xylene exposure. The DFG-MPT-SPE-HPLC method required only 2.00 mg of DFG as adsorbent, 0.50 mL of washing solvent, and 0.40 mL of elution solvent to achieve a wide linear range (0.200-200 µg mL-1), high recoveries (90.9-99.1%), and high precision (RSD ≤ 6.3%). The proposed method was applied to determine HA and MHA in urine samples from occupational workers. Graphical abstract Deep eutectic solvent functionalized graphene oxide composite adsorbent for miniaturized pipette-tip solid-phase extraction of toluene and xylene exposure biomarkers in urine prior to their determination with HPLC-UV.

Combination of highly efficient microflora to degrade paint spray exhaust gas.

Spray paint exhaust gas contains recalcitrant volatile organic compounds (VOCs), such as benzene, toluene and xylene (BTX). Treating BTX with a biofilter often achieves unsatisfactory results because the biofilter lacks efficient microbial community. In this work, three strains for BTX degradation were isolated and identified as Pseudomonas putida, Bacillus cereus and Bacillus subtilis by using 16S rRNA sequencing technology. A consortium of highly efficient microbial community was then constructed on a stable biofilm to treat BTX in a biofilter. A relatively suitable ratio of P. putida, B. cereus and B. subtilis was obtained. An efficiency of over 90% was achieved in the biofilter with VOC concentration of 1000 mg/m3 through inoculation with the microbial community after only 10 days of operation. Thus, fast start-up of the biofilter was realised. Analysis of intermediate products by gas chromatography-mass spectrometry indicated that BTX was degraded into short-chain aldehydes or acids via ring opening reactions.

Record-Setting Selectivity for p-Xylene by an Intrinsically Porous Zero-Dimensional Metallocycle.

In its crystalline state, a dinuclear Cu-based metallocycle discriminates between the three isomers of xylene with liquid-phase selectivity in the order p-xylene ≫ m-xylene ≫ o-xylene. This selectivity holds over a wide concentration range, with p-xylene concentrations as low as 5%. Single-crystal X-ray diffraction and gas chromatography further indicate that the metallocyclic host extracts trace amounts of p-xylene from commercially pure o-xylene (≥99%); using NMR spectroscopy, we show that the metallocycle exhibits exclusive selectivity for p-xylene. Crystallographic studies show that the selectivity is based on the size and shape of the guest in combination with the flexibility of the host.

Sericin-coated polyester based air-filter for removal of particulate matter and volatile organic compounds (BTEX) from indoor air.

Particulate matter and volatile organic compounds have emerged as a prime environmental concern with increasing air pollution in metropolitan cities leading to lung and heart-related issues. This paper describes a facile and novel method for fabrication of polyester based air filter via surface coating with Sericin for imparting effective removal of particulate matter and volatile organic compounds. A simple dip-coating method followed by thermal fixation has been adopted to coat Sericin on the polyester fiber. The developed changes in surface functionality and morphology of the polyester fiber were confirmed by Attenuated total reflection Fourier-transform infrared spectroscopy and Field emission scanning electron microscopy analysis. The fabricated air filter was tested for removal of particulate matter (generated burning incense stick) and volatile organic compounds (generated vaporizing gasoline), in an indoor chamber. The Sericin coated filter was able to remove the PM2.5 and PM 10 (from 1000 µg/m3 level to 5 µg/m3 in a 6.28 m3 chamber) within 27 and 23 min of operation, respectively. The fabricated filter very effectively removed particulate matter for 2160 cycles with intermittent washing. The Sericin-coated air filter also proved very effective for removal of volatile organic compounds (Benzene, Toluene, Ethylbenzene and Xylene) from an indoor chamber at a varying initial concentration of 100-1000 µg/m3. The adsorption behavior was described by Langmuir-Freundlich (sips) isotherm and pseudo-first order kinetics with minimal error. The maximum adsorption capacity (mg/g) obtained with Sips Isotherm fitting followed the order Xylene (6.97)>Ethyl Benzene (5.68)> Toluene (5.35) >Benzene (4.78).

A needle-to-post air discharge ion source in tandem with FAIMS system.

A needle-to-post ionization source was designed for high-field asymmetric waveform ion mobility spectrometry (FAIMS). The needle-to-post ion source includes asymmetric electrode comprised of a copper post with a diameter of 2 mm and a stainless-steel needle with 200-µm tip radius and length of 28 mm. With the discharge voltage of -5.6 kV and N2 gas flow, glow discharge was realized at atmospheric pressure. The mass spectra of ionized ions about acetone, ethanol and ethyl acetate were gotten by Thermo Scientific LTQ XL ion trap mass spectrometer (MS). The MS experimental results show that the main ions are protonated and dimer ions. The needle-to-post ion source was mounted on the FAIMS system and FAIMS spectra are gotten successfully. Separation of p-xylene, o-xylene and m-xylene was realized. It shows that the needle-to-post electrode could be used as the ion source in a FAIMS system.

Changes in bacterial diversity and catabolic gene abundance during the removal of dimethylphenol isomers in laboratory-scale constructed wetlands.

Constructed wetlands (CWs) are well-established wastewater treatment technologies and applied for bioremediation of contaminated water. Despite the optimal performance of CWs, the understanding of the bacterial processes in the rhizosphere, where mainly microbial degradation processes take place, is still limited. In the present study, laboratory-scale CWs planted with Juncus effusus and running under controlled conditions were studied in order to evaluate removal efficiency of dimethylphenols (DMPs), also in comparison to an unplanted bed. Next to removal rates, the bacterial community structure, diversity, and distribution, their correlation with physiochemical parameters, and abundance of the phenol hydroxylase gene were determined. As a result, better removal performance of DMP isomers (3,4-, 3,5-, and 2,6-DMP added as singles compounds or in mixtures) and ammonium loads, together with a higher diversity index, bacterial number, and phenol hydroxylase gene abundance in Juncus effusus CW in comparison with the non-planted CW, indicates a clear rhizosphere effect in the experimental CWs. An enhancement in the DMP removal and the recovery of the phenol hydroxylase gene were found during the fed with the DMP mixture. In addition, the shift of bacterial community in CWs was found to be DMP isomer dependent. Positive correlations were found between the bacteria harboring the phenol hydroxylase gene and communities present with 3,4-DMP and 3,5-DMP isomers, but not with the community developed with 2,6-DMP. These results indicate that CWs are highly dynamic ecosystems with rapid changes in bacterial communities harboring functional catabolic genes.

Lab-In-Syringe automation of stirring-assisted room-temperature headspace extraction coupled online to gas chromatography with flame ionization detection for determination of benzene, toluene, ethylbenzene, and xylenes in surface waters.

Online coupling of Lab-In-Syringe automated headspace extraction to gas chromatography has been studied. The developed methodology was successfully applied to surface water analysis using benzene, toluene, ethylbenzene, and xylenes as model analytes. The extraction system consisted of an automatic syringe pump with a 5 mL syringe into which all solutions and air for headspace formation were aspirated. The syringe piston featured a longitudinal channel, which allowed connecting the syringe void directly to a gas chromatograph with flame ionization detector via a transfer capillary. Gas injection was achieved via opening a computer-controlled pinch valve and compressing the headspace, upon which separation was initialized. Extractions were performed at room temperature; yet sensitivity comparable to previous work was obtained by high headspace to sample ratio VHS/VSample of 1.6:1 and injection of about 77% of the headspace. Assistance by in-syringe magnetic stirring yielded an about threefold increase in extraction efficiency. Interferences were compensated by using chlorobenzene as an internal standard. Syringe cleaning and extraction lasting over 10 min was carried out in parallel to the chromatographic run enabling a time of analysis of <19 min. Excellent peak area repeatabilities with RSD of <4% when omitting and <2% RSD when using internal standard corrections on 100 µg L-1 level were achieved. An average recovery of 97.7% and limit of detection of 1-2 µg L-1 were obtained in analyses of surface water.

Separation of Xylene Isomers through Multiple Metal Site Interactions in Metal-Organic Frameworks.

Purification of the C8 alkylaromatics o-xylene, m-xylene, p-xylene, and ethylbenzene remains among the most challenging industrial separations, due to the similar shapes, boiling points, and polarities of these molecules. Herein, we report the evaluation of the metal-organic frameworks Co2(dobdc) (dobdc4- = 2,5-dioxido-1,4-benzenedicarboxylate) and Co2( m-dobdc) ( m-dobdc4- = 4,6-dioxido-1,3-benzenedicarboxylate) for the separation of xylene isomers using single-component adsorption isotherms and multicomponent breakthrough measurements. Remarkably, Co2(dobdc) distinguishes among all four molecules, with binding affinities that follow the trend o-xylene > ethylbenzene > m-xylene > p-xylene. Multicomponent liquid-phase adsorption measurements further demonstrate that Co2(dobdc) maintains this selectivity over a wide range of concentrations. Structural characterization by single-crystal X-ray diffraction reveals that both frameworks facilitate the separation through the extent of interaction between each C8 guest molecule with two adjacent cobalt(II) centers, as well as the ability of each isomer to pack within the framework pores. Moreover, counter to the presumed rigidity of the M2(dobdc) structure, Co2(dobdc) exhibits an unexpected structural distortion in the presence of either o-xylene or ethylbenzene that enables the accommodation of additional guest molecules.

Comparison of the atmospheric- and reduced-pressure HS-SPME strategies for analysis of residual solvents in commercial antibiotics using a steel fiber coated with a multiwalled carbon nanotube/polyaniline nanocomposite.

A low-cost, sensitive and reliable reduced-pressure headspace solid-phase microextraction (HS-SPME) setup was developed and evaluated for direct extraction of residual solvents in commercial antibiotics, followed by determination by gas chromatography with flame ionization detection (GC-FID). A stainless steel narrow wire was made porous and adhesive by platinization by a modified electrophoretic deposition method and coated with a polyaniline/multiwalled carbon nanotube nanocomposite. All experimental variables affecting the extraction efficiency were investigated for both atmospheric-pressure and reduced-pressure conditions. Comparison of the optimal experimental conditions and the results demonstrated that the reduced-pressure strategy leads to a remarkable increase in the extraction efficiency and reduction of the extraction time and temperature (10 min, 25 °Ï¹ vs 20 min, 40 °Ï¹). Additionally, the reduced-pressure strategy showed better analytical performances compared with those obtained by the conventional HS-SPME-GC-FID method. Limit of detections, linear dynamic ranges, and relative standard deviations of the reduced-pressure HS-SPME procedure for benzene, toluene, ethylbenzene, and xylene (BTEX) in injectable solid drugs were obtained over the ranges of 20-100 pg g-1, 0.02-40 µg g-1, and 2.8-10.2%, respectively. The procedure developed was successful for the analysis of BTEX in commercial containers of penicillin, ampicillin, ceftriaxone, and cefazolin. Graphical abstract Schematic representation of the developed RP-HS-SPME setup.

Control del formaldehído, xileno y compuestos orgánicos volátiles mediante el sistema integral de friocongelación y fotocatalización / Prevention and control of formaldehyde, xylene and volatile organic compounds by photocatalysis and freezing integral system mileida

Antecedentes: En anatomía patológica, existen variedad de agentes químicos que deben ser controlados. Por su potencial cancerígeno destacan el Formaldehído (CH2 O), Xileno y los Compuestos Orgánicos Volátiles (COVs). Objetivo: Valorar la eficacia del uso de purificadores mediante la fotocatalización y los sistemas de friocongelación, para el control de los niveles de exposición a CH2 O, Xileno y COVs. Objetivo Secundario: Comparar mediciones de Formaldehído con otros 3 hospitales de la Comunidad de Madrid. Metodología: Se realizaron 26 mediciones ambientales en Anatomía Patológica del Hospital Universitario de Fuenlabrada (HUF), en febrero del año 2017 y en marzo del mismo año, posterior a la instalación de los purificadores y sistemas de friocongelación, en las áreas de laboratorio y sala de tallado. Se valora Xileno y COVs con el método PID (detector de fotoionización, PID por sus siglas en inglés, PhotoIonization Detector) y de CH2 O a través de un Sistema de Detección de Gas. Como criterio para valorar la exposición a COVs se tomó como gas de referencia el isobutileno con un VLA-EC de 100 ppm. Para el Xileno se compararon los resultados con el VLA-EC 100 ppm y para el CH2 O con el VLA-EC de 0,3 ppm, establecidos en la guía de «Límites de Exposición Profesional para Agentes Químicos» del Instituto Nacional de Seguridad e Higiene en el Trabajo. Resultados: Los niveles de exposición previos no superaban los valores límites. Se observó que tras la implantación de las medidas preventivas colectivas estos valores disminuyeron, obteniéndose resultados estadísticamente significativos: COVs (p= 0.0002; IC 95% 2.393- 5.506), Xileno (p= 0.0002; IC 95% 1.021- 2.359) y CH2 O (p= 0.0004; IC 95% 0.210-0.350). Conclusiones: El sistema integral de friocongelación y purificación mediante fotocatalización optimizan el control de la exposición a dichos agentes químicos, anulando las fuentes de emisión

Background: In anatomical pathology, there are a variety of chemical agents that must be controlled due to their carcinogenic potential, such as formaldehyde (CH2 O), Xylene and Volatile Organic Compounds (VOCs). Objective: To evaluate the effectiveness use of purifiers by photocatalysis and freezing systems for the control of exposure levels to CH2 O, Xylene and VOCs. Secondary Objective: To compare the Formaldehyde measurements among other 3 hospitals in the Community of Madrid. Methodology: 26 environmental assessments were performed in the Anatomical Pathology Department at the Hospital Universitario de Fuenlabrada (HUF, Madrid), in February 2017 and in March of the same year, after installing the purifiers and the freezing systems in the laboratory and room carved areas. Xylene and VOCs are evaluated using the PID method (Photo-Ionization Detector) and CH2 O through a Gas Detection System. As a criterion for assessing exposure to VOCs, isobutylene was used as a reference gas with a VLA-EC of 100 ppm. For Xylene the results were compared with the VLA-EC 100 ppm and for the CH2 O with the VLA-EC of 0.3 ppm, established in the guide of "Occupational Exposure Limits for Chemical Agents" from the National Institute of Occupational Safety and Health. Results: Previous exposure levels did not exceed the limit values. It was observed that these values decreased after the implementation of collective preventive measures, obtaining statistically significant results: VOCs (p = 0,0002, 95% CI 2,393-5,506), Xylene (P = 0,0002, 95% CI 1,021-2,359) and CH2 O (p = 0,0004, 95% CI 0,210-0,350). Conclusions: The integrated system of freeze-thawing and photocatalytic purification optimize the exposure control to these chemical agents, canceling emission sources

Micro-solid phase extraction of benzene, toluene, ethylbenzene and xylenes from aqueous solutions using water-insoluble ß-cyclodextrin polymer as sorbent.

Water-insoluble ß-cyclodextrin polymer was synthesized by chemical cross-linking using epichlorohydrin (EPI) as a cross-linker agent. The produced water-insoluble polymer was used as a sorbent for the micro-solid phase extraction (µ-SPE) of benzene, toluene, ethylbenzene and xylenes (BTEX) from water samples. The µ-SPE device consisted of a sealed tea bag envelope containing 15mg of sorbent. For the evaluation of the extraction efficiency, parameters such as extraction and desorption time, desorption solvent and salt concentration were investigated. At an extraction time of 30min in the course of the extraction process, analytes were extracted from a 10mL aqueous sample solution. The analytes were desorbed by ultrasonication in 200µL of acetonitrile for 20min. Analysis of the analytes was done by a gas chromatography-flame ionization detector (GC-FID) system. The enrichment factor (EF) was found to be in the range 23.0-45.4 (EFmax=50.0). The method provided linearity ranges of between 0.5 and 500.0ng/mL (depending on the analytes), with good coefficients of determination (r2) ranging between 0.997 and 0.999 under optimized conditions. Detection limits for BTEX were in the range of between 0.15 and 0.60ng/mL, while corresponding recoveries were in the range of 46.0-90.0%. The relative standard deviation of the method for the analytes at 100.0ng/mL concentration level ranged from 5.5 to 11.2% (n=5). The proposed method was concluded to be a cost effective and environmentally-friendly extraction technique with ease of operation and minimal usage of organic solvent.

Biodegradation of BTEX Aromatics by a Haloduric Microbial Consortium Enriched from a Sediment of Bohai Sea, China.

This study focused on a haloduric BTEX-degrading microbial consortium EC20 enriched from Bohai Sea sediment. EC20 degraded 87% of BTEX at 435 mg L-1 initial concentration (benzene, toluene, ethylbenzene, and xylenes in equal proportions) in the presence of 3.4% NaCl. 16S rRNA gene-based PCR-DGGE profiles revealed that the dominant bacteria in EC20 were Proteobacteria, Actinobacteria, Bacteroidetes, and Firmicutes at the phylum level, and Pseudomonas, Mesorhizobium, Achromobacter, Stenotrophomonas, and Halomonas at the genus level. PCR detection of genes coding the key enzymes which participated in BTEX degradation pathways showed that the enriched consortium EC20 contained TOL pathway and TOD pathway to initiate biodegradation of BTEX.

Health Issues of Primary School Students Residing in Proximity of an Oil Terminal with Environmental Exposure to Volatile Organic Compounds.

Residential proximity to industrial sites has been associated with adverse effects on human health. Children are more susceptible to airborne environmental exposure because their immune and respiratory systems are still developing. This study aimed to investigate whether living close to an oil terminal in Genoa where there is higher VOCs exposure is associated with an increased rate of school absenteeism because of disease in primary school children. Five schools were chosen for the recruitment of children and students residing in the industrial site (A) were compared to those living in residential sites (B). Sixty-six of the 407 students involved in the project were also selected for VOC monitoring. Source apportionment was carried out by comparing profiles of VOCs; principal component analysis was performed to study the correlation between profiles, and Kriging interpolation model was used to extend profiles to all participants. The concentration means of total VOCs were significantly higher in the industrial areas compared to controls. Adjusting for potential confounders, children who lived in area A had a significantly higher risk of being absent from school due to sore throat, cough, and cold compared to controls. o-Xylene, which is dispersed during the industrial activity, showed clear evidence of a significant association with respiratory symptoms.

Zeolite/iron oxide composite as sorbent for magnetic solid-phase extraction of benzene, toluene, ethylbenzene and xylenes from water samples prior to gas chromatography⬜mass spectrometry.

This study reports a new composite based on ZSM-5 zeolite decorated with iron oxide magnetic nanoparticles as a valuable sorbent for magnetic solid-phase extraction (MSPE). A proposal is made to determine benzene, toluene, ethylbenzene and xylenes (BTEX) as model analytes in water samples using gas chromatography-mass spectrometry. A two-step multivariate optimization strategy, using Plackett⬜Burman and circumscribed central composite designs, was employed to optimize experimental parameters affecting MSPE. The method was evaluated under optimized extraction conditions (i.e., amount of sorbent, 138mg; extraction time, 11min; sample pH, pH of water (i.e., 5.5⬜6.5); eluent solvent volume, 0.5mL; and elution time, 5min), obtaining a linear response from 1 to 100µgL(↙1) for benzene; from 10 to 100µgL(↙1) for toluene, ethylbenzene and o-xylene; and from 10 to 75µgL(↙1) for m,p-xylene. The repeatability of the proposed method was evaluated at a 40µgL(↙1) spiking level and coefficients of variation ranged between 8 and 11% (n=5). Limits of detection were found to be 0.3µgL(↙1) for benzene and 3µgL(↙1) for the other analytes. These values satisfy the current normative of the Environmental Protection Agency and European Union for BTEX content in waters for human consumption. Finally, drinking water, wastewater and river water were selected as real water samples to assess the applicability of the method. Relative recoveries varied between 85% and 114% showing negligible matrix effects.

Achieving synergy between chemical oxidation and stabilization in a contaminated soil.

Eight in situ solidification/stabilization (ISS) amendments were tested to promote in situ chemical oxidation (ISCO) with activated persulfate (PS) in a contaminated soil. A 3% (by weight) dose of all ISS amendments selected for this study completely activated a 1.5% dose of PS within 3 h by raising temperatures above 30 °C (heat activation) and/or increasing pH above 10.5 (alkaline activation). Heat is released by the reaction of CaO with water, and pH increases because this reaction produces Ca(OH)2. Heat activation is preferred because it generates 2 mol of oxidizing radicals per mole of PS, whereas alkaline activation releases only 1. The relative contribution of heat vs. alkaline activation increased with CaO content of the ISS amendment, which was reflected by enhanced contaminant oxidation with increasing CaO content, and was confirmed by comparing to controls promoting purely heat or alkaline (NaOH) activation. The test soil was contaminated with benzene, toluene, ethylbenzene, and xylenes (BTEX) and polycyclic aromatic hydrocarbons (PAH), particularly naphthalene (NAP). ISS-activated PS oxidized between 47% and 84% of the BTEX & NAP, and between 13% and 33% of the higher molecular weight PAH. ISS-activated PS reduced the leachability of BTEX & NAP by 76%-91% and of the 17 PAH by 83%-96%. Combined ISCO/ISS reduced contaminant leachability far than ISCO or ISS treatments alone, demonstrating the synergy that is possible with combined remedies.

Synthetic musk in seafood products from south Europe using a quick, easy, cheap, effective, rugged and safe extraction method.

This study aims at developing a method for the determination of 9 synthetic musk compounds in seafood products by combining the quick, easy, cheap, effective, rugged, and safe (QuEChERS) method and determination by gas chromatography mass spectrometry (GC-EI-MS). Method detection limits (MDL) ranging between 0.001 and 1.94 ng g(-1) were obtained. The linearity is higher than 0.9899 in the range MDL - 100 ng g(-1) with precision below 18% and recoveries between 46% and 120% were obtained. The method was applied to quantify musk compounds in seafood products from the European southwest coast (oysters, mussels, salmon organs, glass eels). Galaxolide and Tonalide exhibited the highest concentration levels ranging between MDL - 96.4 ng g(-1) and MDL - 6.85 ng g(-1), respectively. Contamination levels observed for the two nitro musks (musk xylene and musk ketone) are significantly lower ranging between MDL - 0.6 ng g(-1) and MDL - 0.09 ng g(-1), respectively. Analysis of different organs of salmons showed higher concentrations in liver and gonad than in muscle tissues.

Removal of BTEX by using a surfactant--Bio originated composite.

The application of ostrich bone waste-loaded a cationic surfactant (OBW-OH-CTABr) bioadsorbent for benzene, toluene, ethylbenzene and p-xylene (BTEX) removal from the synthetic and real waters have been studied, and the prepared biomaterials were studied by Fourier transform infrared (FTIR), X-ray diffraction (XRD), surface area measurements (BET), scanning electron microscopy (SEM), Energy-dispersive X-ray spectroscopy (EDX) and point of zero (pH(PZC)). The immobilization of CTABr molecules on the framework of modified OBW showed good tendency to adsorb BTEX from aqueous solution. The exposure time to obtain equilibrium for maximum removal of BTEX was observed to be 60 min. The removal kinetics of BTEX has been evaluated in terms of pseudo-first- and -second-order kinetics, and the Freundlich and Langmuir isotherm models have also been utilized to the equilibrium removal data. The removal process was spontaneous and endothermic in nature and followed pseudo-second-order kinetic model. The immobilized CTABr showed high reusability because of its high adsorption efficiency after 12th cycles. The proposed low-cost bioadsorbent could also be utilized to adsorb BTEX from the real water (Anzali lagoon water). The OBW-OH-CTABr composite is indeed an attractive biomaterial for drinking water-based pollutants and act as an adsorbent for BTEX and oil spills especially in third world due to its low-cost preparation and regeneration and clean processing of the biomaterial with no byproducts after utilize.

Combined removal of a BTEX, TCE, and cis-DCE mixture using Pseudomonas sp. immobilized on scrap tyres.

The simultaneous aerobic removal of a mixture of benzene, toluene, ethylbenzene, and o,m,p-xylene (BTEX); cis-dichloroethylene (cis-DCE); and trichloroethylene (TCE) from the artificially contaminated water using an indigenous bacterial isolate identified as Pseudomonas plecoglossicida immobilized on waste scrap tyres was investigated. Suspended and immobilized conditions were compared for the removal of these volatile organic compounds. For the immobilized system, toluene, benzene, and ethylbenzene were completely removed, while the highest removal efficiencies of 99.0 ± 0.1, 96.8 ± 0.3, 73.6 ± 2.5, and 61.6 ± 0.9% were obtained for o-xylene, m,p-xylene, TCE, and cis-DCE, respectively. The sorption kinetics of contaminants towards tyre surface was also evaluated, and the sorption capacity generally followed the order of toluene > benzene > m,p-xylene > o-xylene > ethylbenzene > TCE > cis-DCE. Scrap tyres showed a good capability for the simultaneous sorption and bioremoval of BTEX/cis-DCE/TCE mixture, implying a promising waste material for the removal of contaminant mixture from industrial wastewater or contaminated groundwater.