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.

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.

Application of hydrophobic extractant in aqueous two-phase systems for selective extraction of cobalt, nickel and cadmium.

This work developed a new and efficient method of extracting and separating Co(II), Ni(II) and Cd(II) in aqueous two-phase systems (ATPS) composed of triblock copolymer (L64)+Na(2)C(4)H(4)O(6)+water and L64+Li(2)SO(4)+water using the hydrophobic extractant 1-nitroso-2-naphtol, which complexes the metal ions and partitions in the triblock copolymer micelles in the ATPS top phase. Metal extraction from the salt-rich phase to the copolymer - rich phase is strongly affected by the fine-tuning of the following parameters: amount of added extractant, type of electrolyte, pH, and tie-line length. Excellent separation factors (S(i,j)) between the metals were obtained at pH=3.00 (S(Co,Cd)=1550 and S(Ni,Cd)=16,700) and pH=1.00 (S(Co,Ni)=826). In the interference study, Co(II) was selectivity extracted in the top phase in the presence of Ni(II) and Cd(II) in a concentration of up to 20 times the cobalt level in the system.

Monosegmented flow analysis exploiting aqueous two-phase systems for the determination of cobalt.

An environmentally safe procedure has been developed for the extraction, separation and determination of metal ions using a monosegmented flow analysis technique that exploits an aqueous two-phase system (ATPS-MSFA). The ATPS-MSFA method was applied for the determination of cobalt, based on the reaction between Co(II) and KSCN, which produces a metallic complex that spontaneously partitions to the top phase of the ATPS composed of poly(ethylene oxide), ammonium sulfate and water. The linear range was 5.00 to 500 µmol kg(-1) (R = 0.9998; n = 13) with a coefficient of variation equal to 1.14% (n = 7). The method yielded a limit of detection and a limit of quantification of 2.17 and 7.24 µmol kg(-1), respectively. The ATPS-MSFA method was applied to the determination of cobalt in a nickel-cadmium battery sample and the results were validity with flame atomic absorption spectrometry using addition standard.

Copper recovery from ore by liquid-liquid extraction using aqueous two-phase system.

We investigated the extraction behavior of Cu(II) in the aqueous two-phase system (ATPS) formed by (L35+MgSO(4)+H(2)O) or (L35+(NH(4))(2)SO(4)+H(2)O) in the presence of the extracting agent 1-(2-pyridylazo)-2-naphthol (PAN). At pH=3 and a PAN concentration of 0.285 mmol kg(-1), both ATPS lead to the effective separation of Cu(II) from other metallic ions (Zn(II), Co(II), Ni(II) and Fe(III)). High separation factors range between 1000 and 10,000 were obtained for the extraction of Cu(II) and concomitant metallic ions. This ATPS was used for the extraction of Cu(II) from a leached ore concentrate with a extraction percentage of 90.4 ± 1.1%; other metals were mainly located in the bottom phase.

Aqueous two-phase systems: a new approach for the determination of p-aminophenol.

A new method has been developed for the spectrophotometric determination of p-aminophenol (PAP) in water, paracetamol formulations and human urine samples with a recovery rate between 94.9 and 101%. This method exploits an aqueous two-phase system (ATPS) liquid-liquid extraction technique with the reaction of PAP, sodium nitroprusside and hydroxylamine hydrochloride in pH 12.0, which produces the [Fe(2)(CN)(10)](10-) anion complex that spontaneously concentrates in the top phase of the ATPS ([Formula in text]). The ATPS does not require an organic solvent, which is a safer and cleaner liquid-liquid extraction technique for the determination of PAP. The linear range of detection was from 5.00 to 500 µg kg(-1) (R ≥ 0.9990; n=8) with a coefficient of variation of 2.11% (n=5). The method exhibited a detection limit of 2.40 µg kg(-1) and a quantification limit of 8.00 µg kg(-1). The ATPS method showed a recovery that ranged between 96.4 and 103% for the determination of PAP in natural water and wastewater samples, which was in excellent agreement with the results of the standard 4-aminoantipyrine method that was performed on the same samples.

A green and sensitive method to determine phenols in water and wastewater samples using an aqueous two-phase system.

A greener and more sensitive spectrophotometric procedure has been developed for the determination of phenol and o-cresol that exploits an aqueous two-phase system (ATPS) using a liquid-liquid extraction technique. An ATPS is formed mostly by water and does not require organic solvent. Other ATPS components used in this study were the polymer, polyethylene oxide, and some salts (i.e., Li(2)SO(4), Na(2)SO(4) or K(2)HPO(4)+KOH). The method is based on the reaction between phenol, sodium nitroprusside (NPS) and hydroxylamine hydrochloride (HL) in an alkaline medium (pH 12.0), producing the complex anion [Fe(2)(CN)(10)](10-) that spontaneously concentrates in the top phase of the system. The linear range was 1.50-500microgkg(-1) (R>or=0.9997; n=8) with coefficients of variation equal to 0.38% for phenol and 0.30% for o-cresol (n=5). The method yielded limits of detection (LODs) of 1.27 and 1.88microgkg(-1) and limits of quantification (LOQs) of 4.22 and 6.28microgkg(-1) for phenol and o-cresol, respectively. Recoveries between 95.7% and 107% were obtained for the determination of phenol in natural water and wastewater samples. In addition, excellent agreement was observed between this new ATPS method and the standard 4-aminoantipyrine (4-AAP) method.