Adsorptive removal of heavy metals from wastewater using Cobalt-diphenylamine (Co-DPA) complex.

Heavy metals like Cadmium, Lead, and Chromium are the pollutants emitted into the environment through industrial development. In this work, a new diphenylamine coordinated cobalt complex (Co-DPA) has been synthesized and tested for its efficiency in removing heavy metals from wastewater, and its adsorption capacity was investigated. The effectiveness of heavy metals removal by Co-DPA was evaluated by adjusting the adsorption parameters, such as adsorbent dose, pH, initial metals concentration, and adsorption period. Heavy metal concentrations in real sample were 0.267, 0.075, and 0.125 mg/L for Cd2+, Pb2+, and Cr3+ before using as-synthesized Co-DPA to treat wastewater. After being treated with synthesized Co-DPA the concentration of heavy metals was reduced to 0.0129, 0.00028, 0.00054 mg/L for Cd2+, Pb2+, and Cr3+, respectively, in 80 min. The removal efficiency was 95.6%, 99.5%, and 99.5% for the respective metals. The adsorption process fitted satisfactorily with Freundlich isotherm with R2(0.999, 0.997, 0.995) for Cd2+, Pb2+, and Cr3+, respectively. The kinetic data obeyed the pseudo-second order for Cd2+ and Cr2+ and the pseudo-first order for Pb2+. Based on the results obtained within the framework of this study, it is concluded that the as-synthesized Co-DPA is a good adsorbent to eliminate heavy metal ions like Cd2+, Pb2+, and Cr3+from wastewater solution. In general, Co-DPA is a promising new material for the removal of heavy metal ions from water.

Recovery and separation of glycyrrhizic acid from Natural Deep Eutectic Solvent (NADES) extract by macroporous resin: adsorption kinetics and isotherm studies.

Natural Deep Eutectic Solvents (NADESs) have emerged as a green and sustainable alternative to conventional organic solvents to extract bioactive compounds. However, the recovery of bioactive compounds from the NADES extracts is challenging, restricting their large-scale applications. The present work investigated the recovery of glycyrrhizic acid (GA) from choline-chloride/lactic acid NADES extract using macroporous resins. GA possesses a wide spectrum of biological activities, and it is extracted from the well-known herb Glycyrrhiza glabra. During resin screening, DIAIONTM SP700 showed high adsorption and desorption capacities. The adsorption kinetics study demonstrated that the adsorption of GA on SP700 followed Pseudo First-order kinetic model. Moreover, the adsorption behaviors were elucidated by the Freundlich isotherm using a correlation coefficient based on a static adsorption study at different temperatures and pH. Furthermore, the thermodynamic parameters, for instance, the change of Gibbs free energy (ΔG*), entropy (ΔS*), and enthalpy (ΔH*), showed that the adsorption process was spontaneous, favorable and exothermic. In addition, the sample after macroporous resin treatment, which is enriched with GA exhibited good anticancer potential analyzed by SRB assay. The regenerated NADES solvent was recycled twice, keeping more than 90% extraction efficiency, indicating good reusability of NADES in the GA extraction process by using macroporous resin.

"Adsorptive removal of Congo Red dye from its aqueous solution by Ag-Cu-CeO2 nanocomposites: Adsorption kinetics, isotherms, and thermodynamics".

Eliminating synthetic dyes and organic contaminants from water is crucial for safeguarding human health and preserving the environment. In this study, we explored the effectiveness of Ag-Cu-CeO2 nanocomposites as adsorbents to remove Congo Red dye from water. Three compositions of Ag-Cu-CeO2 nanocomposites (10:20:70, 15:15:70, and 20:10:70) have been synthesized by the aqueous coprecipitation method. A comprehensive analysis was performed by different techniques including X-ray diffraction, Fourier transform infrared spectroscopy, BET surface area determination, Thermogravimetric analysis, Scanning electron microscopy, and TEM. The synthesized nanocomposites have a dimension of 5 ± 1 nm and a high surface area (51.832-78.361 m2g-1). Among these, the nanocomposite with composition 15:15:70 showed the highest adsorption capacity of 4.71 mg/g adsorption (96.83 % removal) from the 0.8 × 10-4 M (55.6 mg/l) Congo Red solution at pH values of 2 at 20 °C with contact time of 3h. The adsorption data is best fitted in the Freundlich adsorption isotherm and pseudo-second-order kinetic model. The negative values of enthalpy variation (-27.57, -26.43, and -16.73 kJ/mol) demonstrated that the adsorption was spontaneous and exothermic. The cycling run showed a mere 12 % deactivation after five cycles of use thus indicating that Ag-Cu-CeO2 nanocomposites hold great potential as effective and eco-friendly adsorbents to remove Congo Red from water.

Evidence of electronic influence in the adsorption of cationic and zwitterionic dyes on zeolites.

The adsorption of a cationic dye, Methylene blue (MB), and a zwitterionic dye, 8-Hydroxyquinoline (8-HQ), onto zeolites synthesized from different clays has been investigated. The presence of certain metals and the Si/Al ratio of the parent clay has an overall effect on the type of zeolites produced. Zeolites LTA and FAU Y were obtained using the hydrothermal method. X-ray diffraction and Fourier transform infrared spectroscopy (FTIR) spectral analysis was used to study the adsorption phenomena of the adsorbates on the adsorbents. The adsorption profile of MB (Topological Polar Surface Area (TPSA) 43.9 Å2 and 8-HQ (TPSA 33.1 Å2) compared favourably with a Freundlich isotherm with R2 > 0.9 for all the zeolitic materials synthesized. Adsorption capacities of zeolite FAU was significantly different from zeolite LTA for MB removal. The higher adsorption capacity of zeolite FAU was attributed to geometric effects resulting in greater shrinkage in the inter lattice spacing of zeolite LTA leading to a reduction in surface area. Adsorption of the relatively smaller 8-HQ however, did not show significant difference in the two zeolite types. Surface and structural characterization showed that adsorbates/adsorbents interactions were driven by both geometric (inter lattice spacing which imparts higher surface area of the adsorbent) and electronic (electrostatic repulsions through electron back donation from metals in the zeolitic structure) considerations.

Bridged EGFET Design for the Rapid Screening of Sorbents as Sensitisers in Water-Pollution Sensors.

We further simplify the most 'user-friendly' potentiometric sensor for waterborne analytes, the 'extended-gate field effect transistor' (EGFET). This is accomplished using a 'bridge' design, that links two separate water pools, a 'control gate' (CG) pool and a 'floating gate' (FG) pool, by a bridge filled with agar-agar hydrogel. We show electric communication between electrodes in the pools across the gel bridge to the gate of an LND150 FET. When loading the gel bridge with a sorbent that is known to act as a sensitiser for Cu2+ water pollution, namely, the ion exchanging zeolite 'clinoptilolite', the bridged EGFET acts as a potentiometric sensor to waterborne Cu2+. We then introduce novel sensitisers into the gel bridge, the commercially available resins PurometTM MTS9140 and MTS9200, which are sorbents for the extraction of mercury (Hg2+) pollution from water. We find a response of the bridged EGFET to Hg2+ water pollution, setting a template for the rapid screening of ion exchange resins that are readily available for a wide range of harmful (or precious) metal ions. We fit the potentiometric sensor response vs. pollutant concentration characteristics to the Langmuir-Freundlich (LF) model which is discussed in context with other ion-sensor characteristics.

Response of biochar derives from farm waste on phosphorus sorption and desorption in texturally different soils.

The information on changes in phosphorus (P) sorption and desorption characteristics and transformations after biochar application to high P fixing soils is still unclear. In the present study, we evaluated the differential response of biochar derives from five different farm waste viz. Lucaena sp., Albbizia sp., Mangifera indica, Triticum aestivum and Oryza sativa applied at 1 and 3 g kg-1 (w/w) on P sorption and desorption in three texturally different (silt loam, clay loam and sandy loam) soils. The amount of P sorbed by the clay loam was significantly (p<0.05) higher than the silt loam and sandy loam, regardless of added P concentration. The Freundlich isotherms exhibit a better fit (R2 = 0.564-0.996 in silt loam, 0.640-0.993 in clay loam and 0.724-0.993 in sandy loam soil) to P sorption data as compared with the Langmuir isotherm. Biochar application significantly decreased the P desorption maxima and desorption constant. The R2 values ranged from 0.447 to 0.999 in silt loam, 0.438 to 0.996 in clay loam, 0.545 to 0.989 in sandy loam. Lucaena biochar showed highest adsorption maxima, thereby suggesting highest P release, whereas soils treated with Triticum aestivum biochar had the lowest adsorption maxima in both clay loam and sandy loam soil. These results indicated that biochar application can significantly enhance P availability; the extent of which is determined by soil texture and type of biochar. The results of present study highlight that biochar application would help increase soil P availability by enhancing fertilizer-P use efficiency associated with decreased P sorption capacity due to increased flush of available-P in soil colloidal complex.

Surface activity, kinetics, thermodynamics and comparative study of adsorption of selected cationic and anionic dyes onto H3PO4-functionalized bagasse from aqueous stream.

The discharge of dyes into the water body creates toxicity to aquatic organisms because of their aromatic structure and difficult degradation. So, the treatment of dye-contaminated wastewater is required before releasing it. In the present study, thermally treated (600 °C) and H3PO4 (55%)-functionalized bagasse, henceforth called thermochemically activated bagasse (TCAB), was synthesized as potential adsorbent for the effective removal of selected cationic and anionic dyes from their aqueous stream. TCAB characterization was done employing FT-IR, SEM, XRD, zeta potential, BET, and PZC techniques. The comparative study shows that the relative adsorption on TCAB followed the sequence, methyl red (185 mg/g) > safranin (178 mg/g) > congo red (146 mg/g) > brilliant green (139 mg/g) > malachite green (130 mg/g) > bromocresol green (94 mg/g). The adsorption efficiency was investigated concerning the effect of change in TCAB dose (0.05-0.3 g/100 mL), initial dye concentration (20-200 mg/L), pH (4.0-10.0), ionic strength (0.1-0.5 M KCl), urea concentration (0.1-0.5 M) and temperature (25-45 °C). The representative adsorption isotherms belong to typical L-type. The time-dependent dye removal was best explained by the pseudo-second-order (PSO) kinetic model (R2 = 0.9859-0.9991), while equilibrium data were best explained by the Freundlich model (R2 = 0.9881-0.9961). Thermodynamic study showed the spontaneous (ΔG0 <0) and exothermic nature (ΔH0 <0) of the adsorption of different cationic and anionic dyes. The cyclic adsorption ability of TCAB for different dyes was checked up to three cycles (185 to 168 mg/L for MR, 178 to 165 mg/L for SF, 146 to 130 mg/L for CR, 139 to 127 mg/L for BG, 130 to 114 mg/L for MG and 94 to 80 mg/L for BCG), and no significant decrease in the adsorption capacity was noticed. So, the present study provides valuable insights into the adsorption of cationic and anionic dyes onto H3PO4-functionalized bagasse. Addressing the adsorptive aspects enhances the clarity, reliability and applicability of the study's findings and contributes to its overall scientific impact.

Modelling heavy-metal phytoextraction capacities of Helianthus annuus L. and Brassica napus L.

Greenhouse experiments were conducted to test the phytoextraction potential of sunflower (Helianthus annuus L.) and rape (Brassica napus L.) during the initial growth in the heavy metal (i.e., Cd, Ni, Zn, and Pb) contaminated soil. The target plants were grown for 30 d in pots filled up with soil treated with various concentrations of heavy metals. The wet/dry weights of plants and heavy-metal concentrations were measured, and the bioaccumulation factors (BAFs) and Freundlich-type uptake model were then used to measure their capacities of phytoextracting accumulated heavy metals from the soil. It was observed that the wet/dry weights of sunflower and rapeseed decreased, and heavy-metal mass uptake increased in plants commensurate with the elevating heavy metal concentrations in the soil. The sunflower BAF for heavy metals was higher than that of rapeseed. The Freundlich-type uptake model suitably described the phytoextraction capacities of sunflower and rapeseed in a soil contaminated with a single heavy metal and can be used to compare the phytoextraction capacities of different plants for the same heavy metal or of the same plant with different heavy metals. Although this study is based on limited data from two species of plants and soils contaminated with one heavy metal, it provides a basis for evaluating the ability of plants to accumulate heavy metals during their initial growth stages. Additional studies utilizing diverse hyperaccumulator plants and soils polluted with multiple heavy metals are essential to enhance the suitability of the Freundlich-type uptake model for assessing the phytoextraction capacities of intricate systems.

Transport and retention of n-hexadecane in cadmium-/naphthalene-contaminated calcareous soil sampled in a karst area.

Studying the transport of petroleum hydrocarbons in cadmium-/naphthalene-contaminated calcareous soils is crucial to comprehensive assessment of environmental risks and developing appropriate strategies to remediate petroleum hydrocarbons pollution in karst areas. In this study, n-hexadecane was selected as a model petroleum hydrocarbon. Batch experiments were conducted to explore the adsorption behavior of n-hexadecane on cadmium-/naphthalene-contaminated calcareous soils at various pH, and column experiments were performed to investigate the transport and retention of n-hexadecane under various flow velocity. The results showed that Freundlich model better described the adsorption behavior of n-hexadecane in all cases (R2 > 0.9). Under the condition of pH = 5, it was advantageous for soil samples to adsorb more n-hexadecane, and the maximum adsorption content followed the order of: cadmium/naphthalene-contaminated > uncontaminated soils. The transport of n-hexadecane in cadmium/naphthalene-contaminated soils at various flow velocity was well described by two kinetic sites model of Hydrus-1D with R2 > 0.9. Due to the increased electrostatic repulsion between n-hexadecane and soil particles, n-hexadecane was more easily able to breakthrough cadmium/naphthalene-contaminated soils. Compared to low flow velocity (1 mL/min), a higher concentration of n-hexadecane was determined at high flow velocity, with 67, 63, and 45% n-hexadecane in effluent from cadmium-contaminated soils, naphthalene-contaminated soils, and uncontaminated soils, respectively. These findings have important implications for the government of groundwater in calcareous soils from karst areas.

Optimization Study of the Capacity of Chlorella vulgaris as a Potential Bio-Remediator for the Bio-Adsorption of Arsenic (III) from Aquatic Environments.

This study examined the ability of the green microalgae Chlorella vulgaris to remove arsenic from aqueous solutions. A series of studies was conducted to determine the optimal conditions for biological arsenic elimination, including biomass amount, incubation time, initial arsenic level, and pH values. At 76 min, pH 6, 50 mgL-1 metal concentration, and 1 gL-1 bio-adsorbent dosage, the maximum removal of arsenic from an aqueous solution was 93%. The uptake of As (III) ions by C. vulgaris reached an equilibrium at 76 min of bio-adsorption. The maximum adsorptive rate of arsenic (III) by C. vulgaris was 55 mg/gm. The Langmuir, Freundlich, and Dubinin-Radushkevich equations were used to fit the experimental data. The best theoretical isotherm of Langmuir, Freundlich, or/and Dubinin-Radushkevich for arsenic bio-adsorption by Chlorella vulgaris was determined. To choose the best theoretical isotherm, the coefficient of correlation was used. The data on absorption appeared to be linearly consistent with the Langmuir (qmax = 45 mgg-1; R2 = 0.9894), Freundlich (kf = 1.44; R2 = 0.7227), and Dubinin-Radushkevich (qD-R = 8.7 mg/g; R2 = 0.951) isotherms. The Langmuir and Dubinin-Radushkevich isotherms were both good two-parameter isotherms. In general, Langmuir was demonstrated to be the most accurate model for As (III) bio-adsorption on the bio-adsorbent. Maximum bio-adsorption values and a good correlation coefficient were observed for the first-order kinetic model, indicating that it was the best fitting model and significant in describing the arsenic (III) adsorption process. SEM micrographs of treated and untreated algal cells revealed that ions adsorbed on the algal cell's surface. A Fourier-transform infrared spectrophotometer (FTIR) was used to analyze the functional groups in algal cells, such as the carboxyl group, hydroxyl, amines, and amides, which aided in the bio-adsorption process. Thus, C. vulgaris has great potential and can be found in eco-friendly biomaterials capable of adsorbing arsenic contaminants from water sources.

Evaluation of ciprofloxacin (CIP) and clarithromycin (CLA) adsorption with weathered PVC microplastics.

The sorption kinetics of two of the most frequently used antibiotics onto recycled (weathered) polyvinyl chloride (PVC) was investigated, using Freundlich and Langmuir isotherm models. Various experimental conditions were set, including pH, contact time, rotational speed, temperature, and initial concentration. The batch experimental results indicated that Freundlich model was better fitted than Langmuir (R2: 98.7 and 84.7, for CIP and CLA respectively). Maximum adsorption capacity is 45.9 mg/g and 22.0 mg/g for CIP and CLA, respectively. Enthalpy (ΔH), and entropy (ΔS) values were negative for CIP, indicating that the reaction was exothermic and spontaneous, respectively. It was vice versa for CLA. Field emission scanning electron microscope (FESEM) and Fourier transform infrared spectrometer (FT-IR) analysis confirmed the physical adsorption mechanism. The results demonstrated that the recycled PVC microplastic has a good capacity for adsorption for both antibiotics.

pH-equilibration of human hair: Kinetics and pH-dependence of the partition ratios for H+ - and OH- -ions based on a Freundlich isotherm.

Hair is an insoluble, fibrous, α-keratinous, protein composite material, providing outer coverage, e.g., for mammals. In the context of a wider study on the effects of pH on human hair properties, we investigated the time-dependence of pH-equilibration study across the acid and the basic pH-range, using appropriate pure solutions of hydrochloric acid and sodium hydroxide. The results show that pH-equilibration follows essentially equal 1st-order kinetics across the pH-range. The characteristic process time does not change significantly and is in the range of 2.5-5 h. The analysis enables to determine the equilibrium uptakes of H+- and OH- -ions. These follow the expected U-shaped path across the pH-range. For both acidic and alkaline conditions, data are well described by two very similar sorption isotherms of the Freundlich-type. In consequence, partition ratios for both ions are highest near neutrality (pH 7: >6000) and drop off strongly towards low and high pHs (<50). Hair is thus a very strong 'sink' for H+ and OH-. This observation fundamentally challenges traditional views of limited ion uptake, namely, in the mid-pH-range due to hindered diffusion. It also does not support considerations on special roles of certain pHs, specific groups of amino acids, or morphological components. Our analysis thus suggests that established views of the interaction of hair and pH need to be reconsidered, The Freundlich isotherm approach appears to provide a versatile tool to refine our understanding of the interactions of hair and possibly other keratinous materials (horn, nail, feathers) with acids and bases.

Ficus Benjamin's leaf, a native sorbent for the exclusion of Methyl violet 10B from aquatic media.

Due to the use of non-recyclable materials and the high costs of the technologies, removal of dyes from wastewater is becoming more and more pricey. This paper presents the capacity of Ficus Benjamina (FB) leaf powder to eradicate methyl violet dye 10 B (MV) in an aqueous fluid. The surface characteristics and presence of various functional groups on the surface of sorbent were revealed by SEM and FTIR studies. Diverse constraints on the elimination of methyl violet 10 B in an aqueous environment were also studied, including starting dye concentration, temperature, and contact duration. The Elovich & liquid film diffusion models, along with Lagergren first-order, pseudo-second-order, Bangham, and modified Freundlich modeling operated to assess kinetics. Experiments confirmed the pseudo-second-order concept. To investigate tentative data, multiple linear Langmuir, Freundlich, Temkin, as well as two parameters nonlinear isotherm models were applied, with findings indicating that sorption data were like both linear and non-linear isotherms. Sorption data were found to be in excellent agreement with the Freundlich isotherm with R2 value (0.99). The sorption capacity of the sorbent was computed i.e. 312.2 mg/g. Thermodynamic characteristics were also computed. It was concluded that the sorption of methyl violet 10 B sorption on FB leaf powder is exothermic. Hence, it is a potentially cost-effective bio sorbent for exclusion of dye from wastewater.

Effects of liming and different land use types on phosphorus sorption characteristics in acidic agricultural soil of Sodo Zuria Woreda, Southern Ethiopia.

Background: Phosphorus (P) sorption measurements and lime application are of great importance for the sustainable management of P-adsorptive soils. Aim: Therefore, this study aimed to evaluate soil phosphorus sorption under different land-use types and to assess lime input during phosphorus sorption. Treatments include the land use of enclosures, grazing, cultivated and ensut land. Method: Surface soil samples were collected to study the physicochemical properties of specific soils. Lime was mixed with the soils of cultivated land for 30 days. P sorption was subsequently assessed for all land-use types by equilibrating soil samples in 0.01 M CaCl2 containing 30 mL of KH2PO4 at 0, 10, 20, 30, 40, and 50 mg/L. Result: The results showed that land use type had a significant impact on external P demand (EPR). The Langmuir model proved useful information in explaining P sorption. P fixation ranged from 136 to 731.67 mg.kg-1 according to Langmuir model and EPR values ranged from 45.9 to 398.7 mg P kg-1 soil. Exclusory area soil has high sorption compared to other land-use whereas enset land-uses the lowest sorption. The result of correlation analysis revealed that exchangeable Aluminium and clay had positively correlated on P-sorption maximum and SPR of both models. Conclusion: It was concluded that there was a significant difference among land-use systems of P-sorption and there had an influence of lime on acidic soil to reduce EPR. So black market p-fertilizer utilization is not recommended to study site. Liming also restored the soil chemistry of cultivated land. Nevertheless, field trials were proposed to validate mineralization rates and EPR values in cultivated soils.

Synthesis, Characterization, and Application of Dichloride (5,10,15,20-Tetraphenylporphyrinato) Antimony Functionalized Pectin Biopolymer to Methylene Blue Adsorption.

In this work, pectin biopolymers were functionalized with dichloride (5,10,15,20-tetraphenylporphyrinato) antimony [Sb(TPP)Cl2] at various compositions (0.5%, 1%, and 2%). The prepared compounds were characterized with several analytical methods, including X-ray fluorescence (XRF) spectrometry, Fourier-transform infrared spectroscopy (FT-IR), electrospray ionization mass spectrometry (EIS), scanning electron microscope (SEM), X-ray diffraction (XRD), and thermogravimetric-differential thermal (TGA/DTG) analysis. The XRF technique evidenced the presence of Sb metal in the composite beads. FT-IR suggested that the interaction between pectin and the [Sb(TPP)Cl2] complex was assured by inter- and intramolecular C-H⋯O, C-H⋯Cl hydrogen bonds and weak C-H⋯Cg π interactions (Cg is the centroid of the pyrrole and phenyl rings). The morphological features of the prepared polymeric beads were affected by the addition of [Sb(TPP)Cl2] particles, and the surface became rough. The thermal residual mass for the composite beads (29%) was more important than that of plain beads (23%), which confirmed the presence of inorganic matter in the modified polymeric beads. At 20 °C, the highest adsorption amounts of methylene blue were 39 mg/g and 68 mg/g for unmodified pectin and pectin-[Sb(TPP)Cl2] beads, respectively. The adsorption mechanism correlated well with the kinetic equation of the second order and the isotherm of Freundlich. The prepared polymeric beads were characterized as moderate-to-good adsorbents. The calculated thermodynamic parameters demonstrated an exothermic and thermodynamically nonspontaneous mechanism.

Removal of Brilliant Green Dye from Water Using Ficus benghalensis Tree Leaves as an Efficient Biosorbent.

The presence of dyes in water stream is a major environmental problem that affects aquatic and human life negatively. Therefore, it is essential to remove dye from wastewater before its discharge into the water bodies. In this study, Banyan (Ficus benghalensis, F. benghalensis) tree leaves, a low-cost biosorbent, were used to remove brilliant green (BG), a cationic dye, from an aqueous solution. Batch model experiments were carried out by varying operational parameters, such as initial concentration of dye solution, contact time, adsorbent dose, and pH of the solution, to obtain optimum conditions for removing BG dye. Under optimum conditions, maximum percent removal of 97.3% and adsorption capacity (Qe) value of 19.5 mg/g were achieved (at pH 8, adsorbent dose 0.05 g, dye concentration 50 ppm, and 60 min contact time). The Langmuir and Freundlich adsorption isotherms were applied to the experimental data. The linear fit value, R2 of Freundlich adsorption isotherm, was 0.93, indicating its best fit to our experimental data. A kinetic study was also carried out by implementing the pseudo-first-order and pseudo-second-order kinetic models. The adsorption of BG on the selected biosorbent follows pseudo-second-order kinetics (R2 = 0.99), indicating that transfer of internal and external mass co-occurs. This study surfaces the excellent adsorption capacity of Banyan tree leaves to remove cationic BG dye from aqueous solutions, including tap water, river water, and filtered river water. Therefore, the selected biosorbent is a cost-effective and easily accessible approach for removing toxic dyes from industrial effluents and wastewater.

Copper and zinc adsorption from bacterial biomass - possibility of low-cost industrial wastewater treatment.

The increasing interest of all stakeholders to achieve environmental protection with socioeconomic development puts pressure on industrial processes for less negative impact on the environment. The use of biomass for wastewater treatment has increased due to its low costs and technical feasibility. The present study aimed the use of biomass from a waste of known polluted area for the adsorption of Zn and Cu in a fixed-bed reactor. Samples were collected in Cubatão (Brazil) and cultivated in LB medium. Resulting cultivable bacterial communities were identified as Enterococcus faecalis and Pseudomonas aeruginosa. Adsorption experiments were performed varying the metallic ion concentration and the amount of biomass. Adsorption experiments showed efficiency rates up to 90%. As the concentration of metallic ions increased, the adsorption efficiency decreased, indicating that the active sites were saturated. Activated charcoal demonstrated lower adsorption rates than biomass. Elution process showed that HNO3 had better efficiency than HCl. Zn adsorption fitted better for Lineweaver-Burk model (Qmax = 200 mg/g of biomass), while Cu adsorption fitted better for Langmuir model (Qmax = 164 mg/g of biomass). Results here demonstrated that the adsorption of Zn and Cu simulating an industrial wastewater by the biomass from a contaminated area is technically feasible.

Removal of p-cresol using wash waters from lipopeptide production.

This work shows the efficiency of wash waters from lipopeptide production as a remediation strategy to treat urban water samples contaminated with p-cresol. The harvesting step in surfactin production involved a centrifugation step, generating a major soluble fraction and a fraction that is adsorbed to the biomass. The adsorbed fraction was recovered by washing steps. These wash waters containing lipopeptides (mostly surfactins), were successfully used to adsorb and solubilize p-cresol. The method of decontamination applied to an artificially contaminated natural water was monitored using a biosensor based on laccase/magnetic nanoparticles. Given the amount of surfactin within the wash water, the removal of p-cresol from artificially contaminated water was approximately 46.0%. This result confirms the successful and sustainable application of surfactin-rich wash waters to remove p-cresol from artificially contaminated natural water. The adsorption mechanism is potentially based on a multi-layer adsorption process, considering Langmuir and Freundlich adsorption isotherms.

Chromium (VI) bioremoval from contaminated wastewater using Pseudomonas aeruginosa ATHA23 producing biofilm supported on clinoptilolite.

More has yet to be investigated on the increased efficiency of microbes for the removal of heavy metals from industrial wastewaters. The objective was to determine the Cr (VI) bioabsorption and bioreduction ability of biofilm-producing bacteria supported on clinoptilolite from contaminated aqueous solutions. Chromium (VI)-tolerant bacteria, namely Pseudomonas aeruginosa ATHA23, were identified by biochemical methods and 16S rDNA sequencing and were deposited in NCBI (accession number: KF680991). Preparation of clinoptilolite, bacterial growth and isolation, biofilm production including extracellular polysaccharides (EPS) and Cr (VI) removal efficiency, affected by the experimental treatments, were investigated. The use of FTIR characterized clinoptilolite properties with and without biofilm in the presence and absence of Cr (IV). Higher Cr (VI) levels in the bacterial growth medium, increased EPS production with the highest value (0.171 mg L-1), produced 18 h after treating the bacteria with Cr (VI) (100 mg L-1). However, in the absence of Cr (VI), EPS significantly decreased to 0.117 mg L-1. Plackett-Burman and Taguchi statistical analyses were used to optimize the experimental treatments affecting the removal efficiency of Cr (VI). Among the anions (nitrate, sulfate, and chloride), sulfate decreased Cr removal efficiency. The absorption data were best fitted to the pseudo-second order, and the data of Cr adsorption by clinoptilolite-biofilm were also better fitted to Freundlich isotherm model. The Cr (VI) bioremediation potential of P. aeruginosa ATHA23 by the production of biofilm supported on clinoptilolite has been shown for the first time, which is of significance for the environment and the industry.

Total organic carbon content as an index to estimate the sorption capacity of micro- and nano-plastics for hydrophobic organic contaminants.

The worldwide existing micro- and nano-plastics (MNPs) showed high sorption capacity for hydrophobic organic contaminants (HOCs), and thus leading to change of the environmental behaviors and fates of HOCs. However, there is a lack of general index for evaluating the sorption capacity of MNPs for HOCs. Herein, we investigated the sorption of chlorobenzene, naphthalene and phenanthrene to 10 MNPs of different polymer types with and without UV-aging, respectively. It was found that the sorption was well fitted by Freundlich isotherm model with coefficients R2 in the range of 0.892-1.00, and aging of most MNPs resulted in decreased sorption capacity for naphthalene and phenanthrene but slightly increased sorption capacity for chlorobenzene. More importantly, for the 8 MNPs commonly present in the environment and with measured total organic carbon (TOC) covering the range of 23.0-91.9%, the logarithm sorption constant (logKd) values of the studied HOCs positively correlated with TOC contents of MNPs, with a good determination coefficient (R2) of 0.923 for naphthalene, 0.694 for chlorobenzene, and 0.565 for phenanthrene. Our study demonstrated that the TOC content of MNPs is a good index for estimating the contribution of total MNPs to the sorption of nonpolar HOCs in the environmental media.