Monte Carlo, molecular dynamic, and experimental studies of the removal of malachite green using g-C3N4/ZnO/Chitosan nanocomposite in the presence of a deep eutectic solvent.

Deep-eutectic solvents (DES) have emerged as promising candidates for preparing nanocomposites. In this study, a DES-based graphitic carbon nitride (g-C3N4)/ZnO/Chitosan (Ch) nanocomposite was synthesized to remove malachite green (MG) dye from water. The DES was prepared by mixing and heating citric acid as a hydrogen bond acceptor and lactic acid as a hydrogen bond donor. This is the first report of the removal of MG using DES-based nanocomposites. Experiments on kinetics and isothermal adsorption were conducted to systematically explore the adsorption performances of nanocomposite toward dye. At 25 °C, the highest adsorption performance was obtained with alkaline media (>90 % removal). The greatest adsorption capacity (qm) was 59.52 mg g-1 at conditions (30 mg L-1 MG solution, pH 9, 3 mg nanocomposite per 10 mL of MG solution, 25 °C, 150 rpm, and 150 min) based on the calculation from the best-fitting isotherm model (Langmuir). The adsorption process was most appropriately kinetically described by the PSO model. The Monte Carlo (MC) and molecular dynamic (MC) results are correlated with experimental findings to validate the theoretical predictions and enhance the overall understanding of the adsorption process. Electronic structure calculations reveal the nature of interactions, including hydrogen bonding and electrostatic forces, between the nanocomposite and MG molecules.

Graphene oxide intercalated Alk-MXene adsorbents for efficient removal of Malachite green and Congo red from aqueous solutions.

Currently, adsorbents with high adsorption performance for eliminating pollutants from discharged wastewater have received many researchers' attention. To this aim, a novel AMXGO absorbent was fabricated by intercalating graphene oxide (GO) into alkalized MXene (Alk-MXene) layer which exhibited high efficacy for the removal of cationic Malachite Green (MG) and anionic Congo Red (CR). Analysis of FTIR, XRD, SEM and TG presented that AMXGO absorbent have a typical three-dimensional layer by layer structure and abundant oxygen-containing groups and its thermal stability was remarkably improved. BET results elucidated that AMXGO1 adsorbent has larger specific surface area and pore volume (16.686 m2 g-1, 0.04733 cm3 g-1) as compared to Alk-MXene (4.729 m2 g-1, 0.02522 cm3 g-1). A dependence of adsorption performance on mass ratio between Alk-MXene and GO, initial dye concentration, contact time, temperature and pH was revealed. Maximum adsorption capacity of MG (1111.6 mg/g) and CR (1133.7 mg/g) were particularly found for AMXGO1 absorbent with a mass ratio of 3:1 and its removal for both dyes were higher than 92%. The adsorption process of AMXGO1 adsorbent for both MG and CR complies with pseudo-second-order kinetic model and Freundlich isotherm model. In addition, adsorption mechanism was explored that synergism effects as electrostatic attraction, π-π conjugates, intercalation adsorption and pore filling were the main driving force for the high adsorption performance of dye. Therefore, AMXGO adsorbent has a potential application prospect in the purification of dye wastewater.

Enhanced artificial intelligence for electrochemical sensors in monitoring and removing of azo dyes and food colorant substances.

It is necessary to determine whether synthetic dyes are present in food since their excessive use has detrimental effects on human health. For the simultaneous assessment of tartrazine and Patent Blue V, a novel electrochemical sensing platform was developed. As a result, two artificial azo colorants (Tartrazine and Patent Blue V) with toxic azo groups (-NN-) and other carcinogenic aromatic ring structures were examined. With a low limit of detection of 0.06 µM, a broad linear concentration range 0.09µM to 950µM, and a respectable recovery, scanning electron microscopy (SEM) was able to reveal the excellent sensing performance of the suggested electrode for patent blue V. The electrochemical performance of an electrode can be characterized using cyclic and differential pulse voltammetry, and electrochemical impedance spectroscopy. Moreover, the classification model was created by applying binary classification assessment using enhanced artificial intelligence comprises of support vector machine (SVM) and Genetic Algorithm (GA), respectively, a support vector machine and a genetic algorithm, which was then validated using the 50 dyes test set. The best binary logistic regression model has an accuracy of 83.2% and 81.1%, respectively, while the best SVM model has an accuracy of 90.3% for the training group of samples and 81.1% for the test group (RMSE = 0.644, R2 = 0.873, C = 205.41, and = 5.992). According to the findings, Cu-BTC MOF (copper (II)-benzene-1,3,5-tricarboxylate) has a crystal structure and is tightly packed with hierarchically porous nanomaterials, with each particle's edge measuring between 20 and 37 nm. The suggested electrochemical sensor's analytical performance is suitable for foods like jellies, condiments, soft drinks and candies.

Water stable graphene oxide metal-organic frameworks composite (ZIF-67@GO) for efficient removal of malachite green from water.

Malachite green (MG) is extensively applied in aquaculture worldwide as a therapeutic agent. MG and its primary metabolite leucomalachite green (LMG) are commonly detected in aquaculture products. MG can cause serious health concerns (in vivo carcinogenic/genotoxic). The extensive water solubility of MG leads to water pollution and hence it is mandatory to remove MG from water. The current study explores adsorptive removal of MG from water using highly water stable Zeolitic Imidazolate framework/graphene oxide composites (ZIF-67@GO). Adsorption performance of newly synthesized composites is justified for MG removal with excellent results of pseudo second order (R2 = 0.99955) which is well-fitted in this case. ZIF-67@GO data of adsorption isotherm for MG is observed using Freundlich Model (R2 = 0.99999) and with adsorption capacity value observed (134.79 mg/g) with removal efficiency of 99.18%, indicates π-staking and electrostatic association between ZIF-67@GO and MG molecules. Synthesized material has retained reusability while removal efficiency reduced only by 6% after many cycles. Furthermore, factors effecting absorption like contact time, pH, adsorbent dose and quantity and temperature are also determined.

Acrylic acid functionalized graphene oxide: High-efficient removal of cationic dyes from wastewater and exploration on adsorption mechanism.

A novel p(AA)-g-GO material was prepared by grafting polymerization of acrylic acid (AA) onto graphene oxide (GO) skeleton, presenting efficient removal of dyes from wastewater, because the layer spacing of GO is expanded and successfully introduced numerous polar carboxyl groups. The study revealed a rapid adsorption kinetic process and the adsorption capacity for methylene blue (MB) increases with pH, contact time, initial dye concentration and temperature. The maximum adsorption capacity is about 1448.2 mg/g at 25 °C for MB according to the Langmuir isotherm. More importantly, the adsorbent maintains excellent adsorption capacity after five cycles of adsorption-desorption and has remarkable selective separability for methylene blue/methyl orange mixed solution at pH = 10. Furthermore, the equilibrium adsorption capacities for other cationic dyes as malachite green (MG), basic fuchsin (BF) and rhodamine B (RhB) reached 582.1, 571.7 and 437.1 mg/g, respectively. Additionally, the mechanism analysis indicated that electrostatic interactions, π-π conjugation and hydrogen bonding are the predominant forces for adsorbing cationic dyes. Therefore, p(AA)-g-GO is an outstanding adsorbent and has a potential application prospect in the treatment of dye wastewater.

Synthesize of ß-cyclodextrin functionalized dendritic fibrous nanosilica and its application for the removal of organic dye (malachite green).

Dye removal from industrial waste water has become an important issue. The highvisibility, undesirability and recalcitrance are the significant environmental problemfor the dyes. In the present work,ß-cyclodextrin functionalized KCC-1 (KCC-1-NH-ß-CD)was synthesized and utilized to the removal of hazardous malachite green. In order to study the morphology of the synthesized nano adsorbent, Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM) were obtained from the surface of the sample. Additionally, the functionalization of KCC-1 with ß-cyclodextrin was confirmed with Furrier Transform Infrared spectroscopy (FTIR). The textural property of KCC-1 was verified using nitrogen adsorption/ desorption analysis (BET equation). UV-Vis spectroscopy utilized for the investigation of malachite green by KCC-1-NH-ß-CD. Specific surface area of the adsorbent was calculated to be 140 m2 /g and it can be stated that the synthesized nano adsorbent has high removal efficiency. It should be noted that the adsorption capacity of the employed nano adsorbent was more than 95%, which could be attributed to high porosity of ß-cyclodextrin functionalized KCC-1.

Electrospun reduced graphene oxide/TiO2/poly(acrylonitrile-co-maleic acid) composite nanofibers for efficient adsorption and photocatalytic removal of malachite green and leucomalachite green.

Electrospun reduced graphene oxide/TiO2/poly(acrylonitrile-co-maleic acid) composite nanofibers (E-spun RGO/TiO2/PANCMA NFs) were fabricated using electrospinning of the dispersive solution of PANCMA, GO and TiO2 followed by post-chemical reduction. The obtained composite nanofibers were compressed in a dialyzer and then used to absorb and degrade malachite green (MG) and leucomalachite green (LMG) from aqueous solution. Compared to the E-spun TiO2/PANCMA and GO/TiO2/PANCMA NFs, the E-spun RGO/TiO2/PANCMA NFs exhibited higher adsorption capacity and photocatalytic degradation ability. Under optimized conditions, 90.6% of MG and 93.7% of LMG from 50 mL aqueous sample solution were adsorbed on the RGO/TiO2/PANMA NFs (3.0 mg fibers) in 2.0 min, and subsequent the 91.4% and 95.2% of MG and LMG adsorbed on the NFs were degradated in 60 min under UV irradiation, respectively. In addition, the E-spun RGO/TiO2/PANMA NFs exhibited good reusability and could be reused in multiple cycles of operations for adsorption and photocatalytic degradation of MG and LMG. This work demonstrated that the electrospun composite nanofibers are promising materials for removal of pollutants from environmental water samples.

Integration of plasmonic effect into MIL-125-NH2: An ultra-efficient photocatalyst for simultaneous removal of ternary system pollutants.

Industrial effluents often contain mixed metal ions and dyes, and it is difficult to efficiently remove both types of contaminants simultaneously. Here, MIL-125-NH2@Ag/AgCl composites were for the first time developed through a facile deposition-photoreduction method for simultaneously removing Cr(VI)/Rhodamine B (RhB)/Malachite Green (MG) ternary system pollutants under visible-light irradiation. The capacities of Cr(VI) reduction dramatically increased to 98.4% in the coexistence of RhB and MG compared to that of binary (Cr(VI)/RhB (69.6%) or Cr(VI)/MG (67.5%)) and single Cr(VI) (29%) systems. In the meantime, the degradation efficiencies of dyes especially RhB in the ternary system were also improved compared to that of their individual systems. On the grounds of all the experimental results, it can be concluded that the efficient light-harvesting and electrons migration in MIL-125-NH2@Ag/AgCl and the synergistic effect of redox reactions between Cr(VI) and dyes hinder the recombination of photo-induced electron-hole pairs, which are responsible for their high photocatalytic activity to eliminate the mixed pollutants. This study provides a new route to construct high-performance photocatalysts for the practical treatment of wastewater containing mixed pollutants.

Mutual effects behind the simultaneous removal of toxic metals and cationic dyes by interlayer-expanded MoS2 nanosheets.

Simultaneous removal of coexisting metals and dyes from industrial wastewaters is challenging, and the mutual effects behind the co-adsorption of these pollutants remain unclear. Herein, interlayer-expanded MoS2 (IE-MoS2) nanosheets prepared by a one-pot simple and scalable method were tested to simultaneously remove toxic metals and cationic dyes. The adsorption capacities of IE-MoS2 nanosheets were 499, 423, 500, 355, and 276 mg/g for Pb(II), Cu(II), methylene blue, malachite green, and rhodamine B, respectively, in a mono-contaminant system. Interestingly, the sequestration amount of Pb(II) was dependent on the concentrations of dyes in the binary Pb(II)-dye systems, while uptake of cationic dyes was almost not influenced by coexisting Pb(II). The simultaneous adsorption mechanism was further confirmed by spectroscopic methods. The IE-MoS2 nanosheets were easily regenerated and reused for six adsorption-desorption cycles without structure destruction, thus avoiding the potential hazards of nanomaterial to the ecosphere. More interestingly, high-efficiency uptake of Pb(II) from intentionally contaminated natural water and model textile effluent was obtained by using a column filled with IE-MoS2 nanosheets. In summary, IE-MoS2 nanosheets with facile and scalable synthesis method, efficient adsorption performance, and excellent reusability showed potential promise for the integrative treatment of complex wastewater bearing both metals and organic pollutants.

Preparation and Coagulation Performance of Carboxypropylated and Carboxypentylated Lignosulfonates for Dye Removal.

In this work, 1-carboxypropyled (1-CPRLS) and 5-carboxypentyled lignosulfonates (5-CPELS) were synthesized using 2-chlorobutanoic acid and 6-chlorohexanoic acid as carboxylate group donors via SN1 and SN2 mechanisms, respectively. 1-Carboxypropyl and 5-carboxypentyl lignosulfonates with the charge densities of -3.45 and -2.94 meq g-1 and molecular weights of 87,900 and 42,400 g·mol-1 were produced, respectively, under mild conditions. The carboxylate content and degree of substitution (DS) of the 1-CPRLS product were 2.37 mmol·g-1 and 0.70 mol·mol-1, while those of 5-CPELS products were 2.13 mmol·g-1 and 0.66 mol·mol-1, respectively. The grafting of carboxypropyl and carboxypentyl groups to lignosulfonate was confirmed by Fourier transform infrared (FT-IR) and nuclear magnetic resonance (1H-NMR and 13C-NMR) spectroscopies. In addition, 1-CPRLS and 5-CPELS were applied as coagulants for removing ethyl violet (EV) dye from a simulated solution, and their performance was related to their charge densities and molecular weights. Furthermore, fundamental discussion is provided on the advantages of (1) producing 1-CPRLS and (2) the superior properties and performance of 1-CPRLS to carboxyethylated lignosulfonate.

Enhanced decolorization of malachite green by a magnetic graphene oxide-CotA laccase composite.

In this study, a CotA laccase from Bacillus subtilis cjp3 was successfully immobilized onto magnetic graphene oxide (MGO) nanomaterials via covalent bonding with hydrochloride/N-hydroxysuccinimide (EDC/NHS). The morphology, structure, and properties of the MGO-laccase were then characterized by scanning-electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), Fourier-transform infrared spectroscopy (FT-IR), X-ray-photoelectron spectroscopy (XPS), and a magnetic-property-measurement system (MPMS). The magnetic composite exhibited an extremely high binding capacity of ~145.04mg/g and maintained maximal relative enzyme activities at 25°C, pH7, and a reaction time of 2h. The pH, thermal, operational, and storage stabilities of MGO-laccase were significantly improved over those of free laccase. Moreover, MGO-laccase exhibited a higher tolerance than that of free laccase in the presence of organic solvents, inhibitors, metal ions, and salts. Furthermore, MGO-laccase showed good decolorization performance of malachite green (MG), with decolorization rates reaching 99% after 5h of reaction at 30°C and pH6. In addition, the maximum saturation magnetization of MGO-laccase was 27.7emu/g, allowing for rapid magnetic separation. Accordingly, magnetic separation allowed MGO-laccase to maintain 75% of its activity after ten consecutive decolorization cycles.

The roles of Pleurotus ostreatus HAUCC 162 laccase isoenzymes in decolorization of synthetic dyes and the transformation pathways.

Fungal laccases have shown great potential in industrial and environmental applications. They are generally produced as laccase isoenzymes. Thus, to further study the properties of different laccase isoenzymes and their performance in bio-remediation is essential for a deep understanding of laccase function and application. In this study, three Pleurotus ostreatus HAUCC 162 laccase isoenzymes were heterologously expressed, and the effects of different inhibitors, metal ions, and organic solvents on the activity of recombinant laccases were evaluated. In the dye decolorization test, LACC6 showed the highest ability to remove Malachite green (MG), Remazol Brilliant Blue R (RBBR), Bromophenol blue (BB), and Methyl orange (MO) among the three recombinant laccases. Removal rates within 24 h were 91.5%, 84.9%, 79.1%, and 73.1% for MG (100 mg/L), RBBR (100 mg/L), BB (100 mg/L), and MO (100 mg/L), respectively. The MG and RBBR transformation pathways were proposed by using High Performance Liquid Chromatography-Mass Spectrometry (LC-MS) analysis. Based on the results of this work, the production of recombinant LACC6 or improving the portion of LACC6 in the crude extracellular laccase may advance synthetic dye removal.

Efficient decolourization of malachite green with biosynthesized iron oxide nanoparticles loaded carbonated hydroxyapatite as a reusable heterogeneous Fenton-like catalyst.

In this study, iron oxide nanoparticles (IO-NPs) with a mean diameter of 102.85 nm were firstly synthesized via a facile green route using Ulva spp. aqueous extract as a bioreductant agent. Then, IO-NPs were loaded into carbonated hydroxyapatite (c-Hap) and the final product was named as the iron oxide nanoparticles loaded carbonated hydroxyapatite (IO-NPs-Lc-Hap). Subsequently, IO-NPs-Lc-Hap was characterized by FT-IR, SEM, XRD and EDX analysis methods. MG colour removal efficiencies of Ulva spp., Hap, IO-NPs and IO-NPs-Lc-Hap materials were also evaluated by adsorption and/or Fenton-like reaction methods. IO-NPs-Lc-Hap with the highest decolourization capacity was chosen as a heterogeneous Fenton-like catalyst for Malachite Green (MG). For Fenton-like decolourization of MG, the optimum H2O2 concentration, initial dye concentration and catalyst concentration were determined to be 30 mM, 100 mg/L and 1.0 g/L, respectively. At these optimum conditions, 100% decolourization efficiency and 33.3% COD removal were obtained. On the other hand, 94% decolourization efficiency and 42% COD removal were achieved for the real textile wastewater at the obtained optimum conditions. The experimental decolourization reaction rate for MG was determined as -rd = 0.0779 [(mg dye0.3) (g cat-0.3) (min-1)] × qt0.7. Also, the catalyst had high decolourization efficiencies at the end of six sequence usages.

Development of a PRiME cartridge purification method for rapid determination of malachite green and leucomalachite green in Chinese softshell turtle.

A high-throughput PRiME (process, robustness, improvements, matrix effects, ease of use) sample purification procedure was developed to simplify the multiple steps of traditional SPE in extracting the malachite green and leucomalachite green in Chinese softshell turtle (Pelodiscus sinensis). The sample loading volume, extracting solvent type, and pH value of the employed PRiME hydrophilic-lipophilic balance cartridge for sample purification were optimized to be 3 mL, acetonitrile, and pH 5, respectively. In comparison with traditional SPE, the PRiME process is cost-effective, solvent-saving, and simple to operate, which only consists of a passing through step without traditional sorbent conditioning and impurity washing. Afterward, eluate was analyzed by ultra-performance liquid chromatography-tandem mass spectrometry, and the proposed method was validated for linearity (R2 > 0.9992), intraday precision (2.44-3.22%), interday precision (3.28-6.58%), sensitivity (LOD ≤ 0.18 µg/kg and, LOQ ≤ 0.60 µg/kg), and recovery (88.7-94.1%, RSD < 6.79%). The results indicated that the PRiME technique can simplify the sample preparation procedure by avoiding the tedious steps, such as conditioning, washing, etc. It would be of significant interest for environmental and food safety applications in the market of Chinese softshell turtle and related products.

Green one-step synthesis of ZnO/cellulose nanocrystal hybrids with modulated morphologies and superfast absorption of cationic dyes.

Zinc oxide/cellulose nanocrystal (ZnO/CNC) hybrids with modulated morphologies were prepared by using bamboo CNC as templates via green one-step technique. The effect of pH values on the morphology, microstructure, thermal stability, antibacterial efficiency and dye absorption kinetics of hybrids were investigated. A possible mechanism for various hybrid morphologies at different pH values was provided. All the samples exhibited high antibacterial ratios of 91.4%-99.8% against both Escherichia coli and Staphylococcus aureus. ZnO/CNC8.5 gave quick removal efficiency with high dye removal ratios in methylene blue (MB, 93.55%) and malachite green (MG, 99.02%), especially >91.47% and 97.85% within 5 min. The absorption capacity could reach up to 46.77 mg/g for MB and 49.51 mg/g for MG. Besides, absorption kinetics showed that the absorption behavior followed the pseudo-second-order kinetic model (R2 > 0.99996). Such ZnO/CNC hybrids show outstanding and low-cost adsorbent for efficient absorption of cationic dyes in wastewater treatment field.

Removal of malachite green from aqueous solutions using a modified chitosan composite.

The synthesis of a novel composite adsorbent prepared from coir pith activated carbon (CPAC), chitosan and sodium dodecyl sulphate (SDS, an anionic surfactant) is reported. The characterisation of the composite was done using SEM, XRD, UV-visible and IR spectroscopy studies. The effectiveness of the composite was made for the removal of a toxic cationic dye, malachite green (MG) from waste water based on adsorption studies. The reaction conditions for the adsorption studies were optimized based on initial dye concentration, dose rate, reaction time, pH and temperature. Langmuir and Freundlich isotherm models were adopted to study the mechanism of adsorption. The adsorption process was found to follow pseudo second order kinetics. The results of the present study indicate that the CPAC based composite could be an effective low cost adsorbent for the removal of MG from waste water.

Biosynthesis of silver nanoparticles by cell-free extracts from some bacteria species for dye removal from wastewater.

OBJECTIVES: To investigate the biosynthesis of silver nanoparticles (AgNPs) using extracts of some bacterial isolates Bacillus pumilus, Bacillus paralicheniformis and Sphingomonas paucimobilis. The formation of AgNPs was detected by the change in color into yellow and confirmed by the UV-Vis spectroscopy. The nanoparticles were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and Fourier transform infrared spectroscopy (FTIR). RESULTS: The obtained AgNPs were spherical to oval in shape with particle size ranged from 4 to 20 nm and surface area 118 m2/g. The AgNPs have been used as nanocatalyst for the removal of malachite green dye (MG) from aqueous solution. The dye was chosen as a model dye released in wastewater. The AgNPs showed excellent nanocatalyst for the removal of MG. The dye removal process was observed by the continuous decrease in dye absorbance at 617 nm until it vanished over 160 min. The removal kinetics followed closely the pseudo-first-order kinetic model. CONCLUSION: The B. paralicheniformis strain KJ-16 was the most effective isolated bacteria to give extract for biosynthesis of AgNPs and dye removal. This method may be considered easy and eco-friendly, and could be applicable for large-scale decontamination of wastewater from harmful dyes.

Highly-porous diatom biosilica stationary phase for thin-layer chromatography.

This study showed that a nanostructured, highly-porous stationary phase composed of randomly-deposited biosilica frustules isolated from living cells of diatom Pinnularia sp. significantly improved the conventional thin-layer chromatography (TLC) based separation of the triphenylmethane dyes malachite green and fast green relative to silica gel by two mobile phases (9:1:1 v/v 1-butanol:ethanol:water, 5:1:2 v/v 1-butanol:acetic acid:water). Although both stationary phases were composed of amorphous silica rich in silanol groups with particle size of 10-12 µm, diatom biosilica frustules were highly porous, hollow shells with surface structure dominated by 200 nm pore arrays. Diatom biosilica significantly improved the mobility of both malachite green and fast green, enabling the resolution of these analytes. The diatom biosilica layer had a high void fraction of 96% but reduced the flow velocity and permeability constant by a factor of two relative to silica gel. TLC performance was enhanced, as evidenced by ten-fold reduction in theoretical plate height for both analytes using the 1-butanol:acetic acid:water mobile phase, and an increased difference in retention time between malachite green and fast green (ΔRf = 0.26) using the 1-butanol:ethanol:water mobile phase. Analysis of plate height vs. solvent front position by the modified van Deemter equation suggested that dispersive mass transfer was reduced, leading to improved analyte resolution, and that surface of the frustule decreased boundary layer resistance, leading to increased analyte flux. Overall, the basis for improved chromatographic performance is believed to be the unique nano- and microstructure of the diatom biosilica frustule.

Analysis of Triphenylmethane Dye Residues and their Leuco-Forms in Frozen Fish by LC-MS/MS, Fish Microbial Quality, and Effect of Immersion in Whole Milk on Dye Removal.

A rapid and sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was validated and used to quantify crystal violet (CV), leucocrystal violet (LCV), malachite green (MG), leucomalachite green (LMG), and brilliant green (BG) residues in frozen fish (121 samples) from various countries, in order to detect the use of prohibited antibiotic dyes in fish for human consumption. The microbial quality of the fish was also assessed along with the effectiveness of a simple treatment with whole fat milk to reduce the levels of CV and LCV contamination. CV and LCV were the only two residues detected. They were found in farmed Pangasius (0.362 to 41.34 µg/kg and 0.178 to 10.58 µg/kg, respectively) and Tilapia (1.24 to 9.48 µg/kg and 1.29 to 2.81 µg/kg). Based on aerobic plate count (APC), 74%, 59%, and 55% of the samples of Tilapia fillets (from China) and Pangasius fillets (United Arab Emirates and Vietnam), and 100% and 50% of the skin samples of Hake (Argentina and U.S.A.) were of unacceptable microbial quality (APC > 107 cfu/g). Human pathogens, namely Escherichia coli, Staphylococcus aureus, and Vibrio spp., were detected in most fish. A significant reduction in CV and LCV concentrations by more than a third was achieved after immersing Pangasius and Tilapia fillets in whole fat milk for 120 minutes. These findings support the necessity of regular inspections and monitoring of CV and other antibiotic dye residues in fish, along with routine assessments of fish microbial quality, in order to protect public health. PRACTICAL APPLICATION: The described LC-MS/MS method can be used to rapidly and simultaneously quantify antibiotic dye residues in frozen fish. CV and LCV were detected in farmed Pangasius and Tilapia fillets and their concentrations was reduced by more than one third after immersing the fillets in whole milk for 120 min, a treatment which is not intended to replace safe fish farming practices upstream to artificially lower the level of banned dyes in fish. The findings support the necessity of regular inspections and monitoring of CV and other antibiotic dye residues in fish, along with assessments of fish microbial quality, to protect public health.

Burkholderia cepacia immobilized on eucalyptus leaves used to simultaneously remove malachite green (MG) and Cr(VI).

A multifunctional biomaterial capable of simultaneously removing malachite green (MG) and Cr(VI) was prepared by immobilizing Burkholderia cepacia (B. cepacia) on eucalyptus leaves (EL). The maximum uptake of MG (60 mg/L) and Cr(VI) (20 mg/L) were 94.8% and 71.9% respectively, which was more efficient than when using EL or free cells alone. SEM-EDS demonstrated that B. cepacia was attached to EL and that Cr(VI) was biosorbed into the immobilized cells. FTIR showed that the degradation by functional groups of immobilized cells was in keeping with the products, detected by GC-MS, which suggested that MG could be degraded to 4-dimethylamino benzophenone and 4-dimethylamino phenol. The removal of both MG and Cr(VI) by EL immobilized cells fit the pseudo-second order adsorption kinetic model well (with both R2>0.983). The equilibrium adsorption capacity of MG was 9.59, 18.67 and 28.64 mg/g for initial MG concentrations of from 30, 60, 90 mg/L, respectively when the concentration of Cr(VI) was held constant at 20 mg/L. The adsorption capacity of Cr(VI) increased from 3.49, 7.68 to 9.79 mg/g as the initial Cr(VI) concentrations increased (10, 20, 30 mg/L) while the MG concentration was kept constant at 60 mg/L. The results showed that eucalyptus leaves as a low cost and eco-friendly material have some potential to be an effective immobilization for environmental applications.