Adsorption of organic and inorganic arsenic from aqueous solutions using MgAl-LDH with incorporated nitroprusside.

An evaluation was made of the use of MgAl-LDH with incorporated nitroprusside as an adsorbent to remove inorganic arsenic (As(III) and As(V)) and organic arsenic (DMA) from aqueous matrices. The material was synthesized by the co-precipitation method at constant pH and was characterized by Raman spectroscopy, infrared spectroscopy, thermogravimetry, X-ray diffraction, and high-resolution transmission electron microscopy, before and after use in the adsorption process. The effects on adsorption of contact time, initial metalloid concentration, and pH were investigated. For an initial concentration of 10 mg L-1 and pH 2.00, the MgAl-LDH with incorporated nitroprusside was only able to adsorb the DMA and As(V) species, with removal percentages of 25.10 and 103.8%, respectively. At pH 6.02 and 12.00, only the inorganic species were adsorbed, with removal percentages of 22.93% and 60.07%, respectively, for As(III), and 89.81% and 71.64%, respectively, for As(V). Application of the Langmuir and Freundlich isotherm models indicated that the features of the adsorption process depended on the pH of the medium and the arsenic species. The results showed that the use of MgAl-LDH with incorporated nitroprusside has potential for the development of techniques for the speciation of arsenic species.

Anthocyanin immobilization in carboxymethylcellulose/starch films: A sustainable sensor for the detection of Al(III) ions in aqueous matrices.

A robust and sustainable sensor for the detection of Al(III) ions in water was developed by immobilization of anthocyanin (AN) from black rice in a film formed by carboxymethylcellulose (CMC) and starch. Characterization of the films was performed using solubility, thickness, FTIR, and mechanical analysis. The film exhibited an irreversible color change from red to purple in response to the presence of Al(III). The best colorimetric response of the sensor was observed at pH 4.5 and a time of 60 min, achieving the detection of 3 mg L-1 of Al(III). For concentrations higher than 5 mg L-1, the sensor response time decreased to 20 min. The minimum Al(III) concentration detected with the naked eye was lower than the maximum permissible concentrations in aqueous effluents according to different legislations, indicating the potential of this study to develop sensors for the detection of Al(III).

Selective separation of Cu, Ni and Ag from printed circuit board waste using an environmentally safe technique.

Printed circuit boards (PCBs) make up a large part of e-waste and include high concentrations of high-value metals. Therefore, the recovery of these metals is interesting from both the environmental and economic points of view. Here, the extraction/separation of copper, nickel and silver from PCB leachate was studied using an aqueous two-phase system (ATPS) formed by triblock copolymers with an electrolyte and water, which is in compliance with the principles of green chemistry. The best conditions for the selective extraction consisted of 1-(2-pyridylazo)-2-naphthol (3.5 mmol kg-1) at pH = 6.0 in 6 sequential steps for the Cu(II), dimethylglyoxime (5.00 mmol kg-1) at pH = 9.0 for the Ni(II) and thiocyanate (5.20 mmol kg-1) at pH = 9.0 for the Ag(I). These conditions were applied sequentially for extraction of Cu, Ni and Ag from the PCB leachate, obtaining high separation factor (S) values between the analyte and the metallic concomitants (SCu,Ni = 1,460, SCu,Fe = 15,500, SCu,Ag = 15,900, SNi,Fe = 32,700, SNi,Ag = 34,700 and SAg,Fe = 4800). The maximum extraction percentages (%E) for Cu, Ni and Ag were 99.9%, 99.9% and 99.8%, respectively. After the extraction, a single step stripping process was performed, resulting in more than 82% of the ion available in a clean lower phase. For the first time, an ATPS has been used for sequential extraction of several metal analytes from a real sample.

Use of aqueous two-phase PEG-salt systems for the removal of anionic surfactant from effluents.

Linear alkylbenzene sulfonates (LAS) are synthetic anionic surfactants that are extensively used in many industries. As a result, large volumes of effluents containing high levels of these compounds are discharged into water bodies, causing risks to aquatic flora and fauna. Then, there is a need for environmentally safe and economically viable technologies for the removal of LAS from aqueous matrices. The present work evaluates the use of aqueous two-phase systems (ATPS) composed of PEG and sulfate salts for this purpose, considering the effects of tie line length (TLL), molar mass of polymer, and type of cation-forming salt on the partitioning behavior of LAS. All the LAS partition coefficient (KLAS) values were greater than unity, and the LAS extraction efficiencies (%ELAS) were higher than 97%. The system consisting of PEG 1500 + (NH4)2SO4 + H2O provided the highest KLAS (1083.34) and %ELAS (99.9%), indicating that the method provided good extraction of LAS to the top phase. This system was applied using a real effluent sample in laboratory-scale experiments as well as in bench-scale batch trials. The results obtained at the laboratory scale showed %ELAS values greater than 98%, while the best KLAS value obtained in the batch experiments was 8.50 (±1.75) (%ELAS = 78.17%). These values demonstrated the potential of ATPS for the removal of LAS from industrial effluents.

A method for dye extraction using an aqueous two-phase system: Effect of co-occurrence of contaminants in textile industry wastewater.

This paper reports a green and efficient procedure for extraction of the dyes Malachite Green (MG), Methylene Blue (MB), and Reactive Red 195 (RR) using an aqueous two-phase system (ATPS). An ATPS consists mainly of water, together with polymer and salt, and does not employ any organic solvent. The extraction efficiency was evaluated by means of the partition coefficients (K) and residual percentages (%R) of the dyes, under different experimental conditions, varying the tie-line length (TLL) of the system, the pH, the type of ATPS-forming electrolyte, and the type of ATPS-forming polymer. For MG, the best removal (K = 4.10 × 10(4), %R = 0.0069%) was obtained with the ATPS: PEO 1500 + Na2C4H4O6 (TLL = 50.21% (w/w), pH = 6.00). For MB, the maximum extraction (K = 559.9, %R = 0.258%) was achieved with the ATPS: PEO 400 + Na2SO4 (TLL = 50.31% (w/w), pH = 1.00). Finally for RR, the method that presented the best results (K = 3.75 × 10(4), %R = 0.237%) was the ATPS: PEO 400 + Na2SO4 (TLL = 50.31% (w/w), pH = 6.00). The method was applied to the recovery of these dyes from a textile effluent sample, resulting in values of K of 1.17 × 10(4), 724.1, and 3.98 × 10(4) for MG, MB, and RR, respectively, while the corresponding %R values were 0.0038, 0.154, and 0.023%, respectively. In addition, the ATPS methodology provided a high degree of color removal (96.5-97.95%) from the textile effluent.

Synthesis and application of a new carboxylated cellulose derivative. Part I: Removal of Co(2+), Cu(2+) and Ni(2+) from monocomponent spiked aqueous solution.

A new carboxylated cellulose derivative (CTA) was prepared from the esterification of cellulose with 1,2,4-Benzenetricarboxylic anhydride. CTA was characterized by percent weight gain (pwg), amount of carboxylic acid groups (nCOOH), elemental analysis, FTIR, TGA, solid-state (13)C NMR, X-ray diffraction (DRX), specific surface area, pore size distribution, SEM and EDX. The best CTA synthesis condition yielded a pwg and nCOOH of 94.5% and 6.81mmolg(-1), respectively. CTA was used as an adsorbent material to remove Co(2+), Cu(2+) and Ni(2+) from monocomponent spiked aqueous solution. Adsorption studies were developed as a function of the solution pH, contact time and initial adsorbate concentration. Langmuir model better fitted the experimental adsorption data and the maximum adsorption capacities estimated by this model were 0.749, 1.487 and 1.001mmolg(-1) for Co(2+), Cu(2+) and Ni(2+), respectively. The adsorption mechanism was investigated by using isothermal titration calorimetry. The values of ΔadsH° were in the range from 5.36 to 8.09kJmol(-1), suggesting that the mechanism controlling the phenomenon is physisorption. Desorption and re-adsorption studies were also performed. Desorption and re-adsorption efficiencies were closer to 100%, allowing the recovery of both metal ions and CTA adsorbent.

Aqueous two-phase systems: an efficient, environmentally safe and economically viable method for purification of natural dye carmine.

Partition of the natural dye carmine has been studied in aqueous two-phase systems prepared by mixing aqueous solutions of polymer or copolymer with aqueous salt solutions (Na(2)SO(4) and Li(2)SO(4)). The carmine dye partition coefficient was investigated as a function of system pH, polymer molar mass, hydrophobicity, system tie-line length and nature of the electrolyte. It has been observed that the carmine partition coefficient is highly dependent on the electrolyte nature and pH of the system, reaching values as high as 300, indicating the high potential of the two-phase extraction with ATPS in the purification of carmine dye. The partition relative order was Li(2)SO(4)"Na(2)SO(4). Carmine molecules were concentrated in the polymer-rich phase, indicating an enthalpic specific interaction between carmine and the pseudopolycation, which is formed by cation adsorption along the macromolecule chain. When the enthalpic carmine-pseudopolycation interaction decreases, entropic forces dominate the natural dye-transfer process, and the carmine partitioning coefficient decreases. The optimization of the extraction process was obtained by a central composite face-centered (CCF) design. The CCF design was used to evaluate the influence of Li(2)SO(4) and PEO 1500 concentration and of the pH on the partition coefficient of carmine. The conditions that maximize the partition of carmine into the top phase were determined to be high concentrations of PEO and Li(2)SO(4) and low pH values within the ranges studied.