Selective separation of Cr(III) and Fe(III) from liquid effluents using a chelating resin

2012 ◽  
Vol 66 (9) ◽  
pp. 1968-1976 ◽  
Author(s):  
Sandra Fernandes ◽  
Inês S. Romão ◽  
Carlos M. R. Abreu ◽  
Margarida J. Quina ◽  
Licínio M. Gando-Ferreira

This study aimed to assess the selective separation of Cr(III) from Fe(III) from liquid solutions by using a chelating ion exchange resin, Diaion CR 11, from Mitsubishi Chemical Corporation, in the H+ form. Equilibrium experiments with synthetic solutions of iron and chromium were carried out in batch mode. For both metals favorable adsorption isotherms were obtained, and the experimental data were well described by the Langmuir model. However, the resin exhibited higher affinity for iron than for chromium. The regeneration experiments revealed that, for both metals, HCl provided higher removal efficiencies than H2SO4 and HNO3. Moreover, precipitation with NaOH allows selectively separate chromium and iron to be stripped from the resin. Experiments in fixed bed operation were carried out to assess the dynamic behavior of the sorption of Cr(III) and Fe(III) into the tested resin by using synthetic and industrial solutions. The experiments with industrial effluent showed that the resin can remove low levels of contaminant transition metal ions, and thus the effluent can be purified for reuse of chromium during periods of 20–25 min. The resin regeneration was achieved with a sequential treatment with HCl and NaOH/H2O2. High efficiencies were observed for both monocomponent and multicomponent systems. A global strategy for separating and recovering Cr(III) from an effluent that also contains Fe(III) is presented, involving the integration of ion exchange (saturation and regeneration phases) and precipitation processes. In conclusion, our approach demonstrates that efficient separation of chromium and iron is possible if ion exchange operation in a fixed bed configuration is optimized and combined with conventional processes such as precipitation.

Author(s):  
Abdelhamid Addala ◽  
Moussa Boudiaf ◽  
Maria Elektorowicz ◽  
Embarek Bentouhami ◽  
Yacine Bengeurba

Abstract Under varied conditions, the IRC 718 ion-exchange resin is used to extract chromium (VI) ions from aqueous solutions. On chromium (VI) removal effectiveness, the effects of adsorption dosage, contact time, beginning metal concentration, and pH were examined. The batch ion exchange process reached equilibrium after around 90 minutes of interaction. With an initial chromium (VI) concentration of 0.5 mg/dm3, the pH-dependent ion-exchange mechanism revealed maximal removal in the pH 2.0–10 range . The adsorption mechanism occurs between Cr(VI) determined as the electron acceptor, and IRC 718 determined as the electron donor. The equilibrium ion-exchange potential and ion transfer quantities for Amberlite IRC 718 were calculated using the Langmuir adsorption isotherm model. The overall ion exchange capacity of the resin was determined to be 187.72 mg of chromium (VI)/g of resin at an ideal pH of 6.0.


2003 ◽  
Vol 75 (3) ◽  
pp. 169-177 ◽  
Author(s):  
R. Al-Merey ◽  
Z. Hariri ◽  
J. Abu Hilal

Eng ◽  
2021 ◽  
Vol 2 (4) ◽  
pp. 512-530
Author(s):  
Alex L. Riley ◽  
Christopher P. Porter ◽  
Mark D. Ogden

The extraction of Cu from mixed-metal acidic solutions by the thiourea-functionalized resin Puromet MTS9140 was studied. Despite being originally manufactured for precious metal recovery, a high selectivity towards Cu was observed over other first-row transition metals (>90% removal), highlighting a potential for this resin in base metal recovery circuits. Resin behaviour was characterised in batch-mode under a range of pH and sulphate concentrations and as a function of flow rate in a fixed-bed setup. In each instance, a high selectivity and capacity (max. 32.04 mg/g) towards Cu was observed and was unaffected by changes in solution chemistry. The mechanism of extraction was determined by XPS to be through reduction of Cu(II) to Cu(I) rather than chelation. Elution of Cu was achieved by the use of 0.5 M–1 M NaClO3. Despite effective Cu elution (82%), degradation of resin functionality was observed, and further detailed through the application of IC analysis to identify degradation by-products. This work is the first detailed study of a thiourea-functionalized resin being used to selectively target Cu from a complex multi-metal solution.


2020 ◽  
Vol 11 (10) ◽  
pp. 5467-5481 ◽  
Author(s):  
Thomas J. Robshaw ◽  
Keith Bonser ◽  
Glyn Coxhill ◽  
Robert Dawson ◽  
Mark D. Ogden

Abstract This work aims to contribute to addressing the global challenge of recycling and valorising spent potlining; a hazardous solid waste product of the aluminium smelting industry. This has been achieved using a simple two-step chemical leaching treatment of the waste, using dilute lixiviants, namely NaOH, H2O2 and H2SO4, and at ambient temperature. The potlining and resulting leachate were characterised by spectroscopy and microscopy to determine the success of the treatment, as well as the morphology and mineralogy of the solid waste. This confirmed that the potlining samples were a mixture of contaminated graphite and refractory materials, with high variability of composition. A large quantity of fluoride was solublised by the leaching process, as well as numerous metals, some of them toxic. The acidic and caustic leachates were combined and the aluminium and fluoride components were selectively extracted, using a modified ion-exchange resin, in fixed-bed column experiments. The resin performed above expectations, based on previous studies, which used a simulant feed, extracting fluoride efficiently from leachates of significantly different compositions. Finally, the fluoride and aluminium were coeluted from the column, using NaOH as the eluent, creating an enriched aqueous stream, relatively free from contaminants, from which recovery of synthetic cryolite can be attempted. Overall, the study accomplished several steps in the development of a fully-realised spent potlining treatment system. Graphic Abstract


1999 ◽  
Vol 30 (3) ◽  
pp. 258-264 ◽  
Author(s):  
K. Madhavan Nampoothiri ◽  
Ashok Pandey

Investigations were carried out with the aim of producing L-glutamic acid from Brevibacterium sp. by utilizing a locally available starchy substrate, cassava (Manihot esculenta Crantz). Initial studies were carried out in shake flasks, which showed that even though the yield was high with 85-90 DE (Dextrose Equivalent value), the maximum conversion yield (~34%) was obtained by using only partially digested starch hydrolysate, i.e. 45-50 DE. Fermentations were carried out in batch mode in a 5 L fermenter, using suitably diluted cassava starch hydrolysate, using a 85-90 DE value hydrolysate. Media supplemented with nutrients resulted in an accumulation of 21 g/L glutamic acid with a fairly high (66.3%) conversation yield of glucose to glutamic acid (based on glucose consumed and on 81.74% theoretical conversion rate). The bioreactor conditions most conducive for maximum production were pH 7.5, temperature 30°C and an agitation of 180 rpm. When fermentation was conducted in fed-batch mode by keeping the residual reducing sugar concentration at 5% w/v, 25.0 g/L of glutamate was obtained after 40 h fermentation (16% more the batch mode). Chromatographic separation by ion-exchange resin was used for the recovery and purification of glutamic acid. It was further crystallized and separated by making use of its low solubility at the isoelectric point (pH 3.2).


1992 ◽  
Vol 26 (1-2) ◽  
pp. 189-196 ◽  
Author(s):  
C. N. Mazidji ◽  
B. Koopman ◽  
G. Bitton

A chelating resin (Chelex 50-100) and ion-exchange resin (Dowex 50W-X8) were evaluated for removal of heavy metals in toxicity fractionation. Microtox and β-galactosidase activity were employed as toxicity endpoints. The resins were packed into 4 raL glass Pasteur pipettes for use. Chelating resin provided complete removal of toxicity due to polyvalent heavy metal cations (Cd, Cu, Hg, Pb, Zn). Ion-exchange resin was ineffective in removing mercury toxicity. Neither resin provided complete removal of Ag+ toxicity. Toxicity of organic compounds was, at most, partially removed. Performance of the ion-exchange and chelating resins was insensitive to hardness and pH. Based on these results, chelating resin is recommended for heavy metal removal as part of a toxicity fractionation procedure.


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