Ismail M. M. Rahman

Non-destructive separation of metal ions from wastewater containing excess aminopolycarboxylate chelant in solution with an ion-selective immobilized macrocyclic material

Although the excellent metal-binding capacities of aminopolycarboxylate chelants (APCs) facilitate their extensive use, pre- and post-toxicity of APCs and their high persistence in aquatic environments evoke concerns. Several treatment techniques with a principal focus on the degradation of APCs at the pre-release step have been proposed. Here, we report a technique for the separation of metal ions from waste solution containing excess APCs using a solid phase extraction system with an ion-selective immobilized macrocyclic material, commonly known as a molecular recognition technology (MRT) gel. Synthetic metal solutions with 100-fold chelant content housed in H2O matrices were used as samples. The MRT gel showed a higher recovery rate compared with other SPE materials at 20 degrees C using a flow rate of 0.2 mL min(-1). The effects of solution pH, metal-chelant stability constants and ionic radii were assessed for 32 metals. Compared to the conventional treatment options for such waste solutions, our proposed technique has the advantage of non-destructive separation of both metal ions and chelants.

Selective separation of arsenic species from aqueous solutions with immobilized macrocyclic material containing solid phase extraction columns.

A combination of solid phase extraction (SPE) columns was used for selective separation of water-soluble arsenic species: arsenite, arsenate, monomethylarsonic acid (MMA) and dimethylarsinic acid (DMA). The SPE columns, namely AnaLig TE-01 (TE-01), AnaLig AN-01 Si (AN-01) and AnaLig As-01 PA (As-01), contain immobilized macrocyclic material as the sorbent and commonly known as molecular recognition technology (MRT) gel. The retention, extraction and recovery behavior of the MRT gel SPE columns were studied at pH 4-10. Fortified deionized water spiked with 100 μM of arsenic species were treated at the flow rate of 0.2 mL min⁻¹. HNO₃ (1.0 and 6.0 M) was used as eluent to recover the retained arsenic species from TE-01 and AN-01 SPE columns. Arsenic species retained in the As-01 column were eluted with HNO₃ (0.1 M) followed by NaOH (2.0 M). Likely interference from the various coexisting ions (Na(+), K(+), Ca²(+), Mg²(+), Cl⁻, NO₃⁻, CH₃COO⁻, PO₄³⁻, SO₄²⁻, ClO₄⁻) (10 mM) were negligible. Quantitative separation of As(III), As(V), MMA and DMA was achieved based on the differences in extraction and recovery behavior of the MRT gel SPE columns with pH for different arsenic species. Complexation between arsenic species and MRT gel is the core phenomenon of the proposed technique as the complexation of MRT gels is expected to be stronger than the resin-based separation processes. MRT gel SPE columns are advantageous as compared with other reported SPE columns in terms of its performance with As(III). Effortless regeneration and unaltered separation performance of the sorbent materials for more than 100 loading and elution cycles are other sturdy characteristics to consider the MRT gel SPE columns for sensitive and selective arsenic species separation.

Effect of Extraction Variables on the Biodegradable Chelant-Assisted Removal of Toxic Metals from Artificially Contaminated European Reference Soils

Development of aminopolycarboxylate chelants (APCs) having enhanced biodegradability is gaining increasing focus to replace the EDTA and its homologs with those used widely for the ex situ treatment of contaminated soils and are potential eco-threats. The paper reports the chelant-assisted extraction of the toxic metals (Cd, Cu, Pb, and Zn) from the metal-spiked European reference soils (Eurosoil 1 and Eurosoil 4) using biodegradable APCs, namely EDDS, GLDA, and HIDS. The effects of chelant-to-metal molar ratio, solution pH, and metal/chelant stability constants were evaluated, and compared with that of EDTA. The selectivity aptitude of the biodegradable chelants towards the toxic metals was assumed from the speciation calculations, and a proportionate correlation was observed at neutral pH. Pre- and post-extractive solid phase distributions of the target metals were defined using the sequential extraction procedure and dissolution of metals from the theoretically immobilized fraction was witnessed. The effect of competing species (Al, Ca, Fe, Mg, and Mn) concentrations was proven to be minimized with an excess of chelant in solution. The highlight of the outcomes is the superior decontamination ability of GLDA, a biodegradable APC, at minimum chelant concentration in solution and applicability at a wide range of pH environments.

Decontamination of spent iron-oxide coated sand from filters used in arsenic removal

Sand filters devised with iron-rich adsorbents are extensively promoted and deployed in the arsenic-prone south and south-east Asian countries (e.g., Bangladesh). The approach offers superior performance in removing arsenic while the spent sludge from the sand filters is an issue of concern due to the possibility of toxic releases after being discarded. In this work, a new technique is proposed for the treatment of spent iron-oxide coated sand (IOCS) from filters used in arsenic removal. Chelant-washing of the arsenic-loaded IOCS is combined with the solid phase extraction treatment to accomplish the objective. The unique point of the proposed process is the cost-effective scheme, which includes the option of recycling of the washing solvent beside the decontamination of the spent arsenic-rich sludge.

Chelant-induced reclamation of indium from the spent liquid crystal display panels with the aid of microwave irradiation.

Indium is a rare metal that is mostly consumed as indium tin oxide (ITO) in the fabrication process of liquid crystal display (LCD) panels. The spent LCD panels, termed as LCD-waste hereafter, is an increasing contributor of electronic waste burden worldwide and can be an impending secondary source of indium. The present work reports a new technique for the reclamation of indium from the unground LCD-waste using aminopolycarboxylate chelants (APCs) as the solvent in a hyperbaric environment and at a high-temperature. Microwave irradiation was used to create the desired system conditions, and a substantial abstraction of indium (≥80%) from the LCD-waste with the APCs (EDTA or NTA) was attained in the acidic pH region (up to pH 5) at the temperature of ≥120 °C and the pressure of ~50 bar. The unique point of the reported process is the almost quantitative recovery of indium from the LCD-waste that ensured via the combination of the reaction facilitatory effect of microwave exposure and the metal extraction capability of APCs. A method for the selective isolation of indium from the extractant solution and recycle of the chelant in solution is also described.

Determination of lead in solution by solid phase extraction, elution, and spectrophotometric detection using 4-(2-pyridylazo)-resorcinol

AbstractLead (+2) was selectively adsorbed on a solid phase extraction (SPE) gel (molecular recognition technology, MRT), quantitatively extracted, and spectrophotometrically determined as the Pb(II)-PAR (4-(2-pyridylazo)-resorcinol) complex. The linear range was 0.01 to 0.75 mg L−1 and the detection limit was 6.4 µg L−1. The MRT-SPE allows selective Pb(II) extraction from complex ion-rich matrices, which is difficult with other techniques. Interference from common matrix ions such as Fe2+, Ni2+, Cu2+ or Co2+ is minimized.

Selective separation of some ecotoxic transition metal ions from aqueous solutions using immobilized macrocyclic material containing solid phase extraction system

The original version of the article was published in Cent. Eur. J. Chem. 9(6) (2011), pp 1019–1026. Unfortunately, the original version of this article contains mistakes in the body of Fig. 1. Here we display the corrected version of the Fig. 1.

Chelant-Assisted Depollution of Metal-Contaminated Fe-Coated Sands and Subsequent Recovery of the Chemicals Using Solid-Phase Extraction Systems

The disposal of potentially toxic element (PTE)-loaded sludge that is produced during industrial or commercial wastewater treatments evoke concerns because of the probability of hazardous environmental consequences. In the current work, we proposed a chelant-assisted decontamination technique of the laboratory-produced PTE-loaded (As, Cd, Pb) polymeric-Fe-coated sludge and subsequent recovery of the chelants and PTEs. The chelant options include both biodegradable (EDDS, GLDA, and HIDS) and non-biodegradable (EDTA) alternatives. The washing performance was compared and discussed in terms of the solution pH and relative stabilities of the complexes of PTEs and chelants in solution. The changes in solution pH or chelants have no significant effect on the chelant-induced removal efficiency of Cd, and the same result was observed for Pb at extreme and moderate acidic pH. The As-extraction rate is also improved with chelant in the solution despite a limited interaction between the chelant and the arsenic species in the solution. The column-packed solid-phase extraction (SPE) system, which was equipped with macrocycle, chelating resin, or ion-exchange resin, was used to explore the corresponding separation performance of the PTEs and chelant. The macrocycle-equipped SPE system shows better selectivity than other SPEs in terms of extraction and recovery performance of the PTEs regardless of the chelants. Some unique points of the proposed process are minimum environmental burden due to the use of biodegradable materials in the washing solution and cost minimization by recycling the ingredients.

A silica gel-bound macrocycle system for the selective separation of toxic cadmium from metal-affluent aqueous matrix

Selective separation of cadmium(II) on a macrocycle immobilized solid phase extraction (SPE) system namely AnaLig Cd-01, and commonly known as molecular recognition technology (MRT) gel, have been examined. The MRT-SPE able to retain the cadmium from the metal-affluent aqueous matrix at the pH range of 2 to 8, and the captured species can be recovered via elution with 1 and 6 M HNO3. Besides the effects of solution pH and eluent concentration, the impacts of sample loading flow rates and coexisting matrix ions were also investigated and optimized. The Cd(II) retention capacity of the MRT-SPE was 0.26 mmol g-1, and it can be reused for more than 100 loading and elution cycles. The Cd(II) recovery attained from the metal-spiked natural waters was satisfactory (95.3–98.1%). However, the Cd(II) retention ability of the MRT-SPE was significantly decreased when excess of chelant remain in the aqueous waste matrix.Graphical abstract

Chemical-Induced Washing Remediation of Metal-Contaminated Soils

The immobilization or removal of toxic components using aqueous extractants, with or without additives, is one of the commonly practiced techniques for the treatment of metal-contaminated soils. However, rather than the use of water alone, the solution with chemical-additives is preferred due to the less time requirement and better separation effectiveness. There is a long-favored list of additives that have been used for the chemical-induced washing remediation of soils, which include acids, bases, chelants, surfactants, and so forth. The objective of this chapter is to provide a brief overview of the chemical-assisted soil washing approaches.