Biosorption of copper using nopal fibres: moolooite formation and magnesium role in the reactive crystallization mechanism
In this contribution, we present findings on biosorption of Cu (II) ions using novel alkali-treated nopal fibres. The biosorption data at equilibrium were fitted to several isotherm models and the biosorbent was characterized by XRD and SEM–EDX. The biosorption mechanism was investigated using a hol...
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Published in: | Cellulose (London) Vol. 27; no. 17; pp. 10259 - 10276 |
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Main Authors: | , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Dordrecht
Springer Netherlands
01-11-2020
Springer Nature B.V |
Subjects: | |
Online Access: | Get full text |
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Summary: | In this contribution, we present findings on biosorption of Cu (II) ions using novel alkali-treated nopal fibres. The biosorption data at equilibrium were fitted to several isotherm models and the biosorbent was characterized by XRD and SEM–EDX. The biosorption mechanism was investigated using a holistic approach of pH shifts, apparent colour variations and changes in the concentration of Cu(II) and dissolved hard ions (calcium and magnesium) in the Cu(II) solution. The correlation between the colour, XRD analysis, pH shifts and hard cations released from the biosorbent into the solution suggested the existence of two crystal formations, malachite and moolooite, in what appears to be a microprecipitation mechanism via reactive crystallization. The role of magnesium during the transformation of malachite into moolooite during the copper binding mechanism is analysed. Magnesium cations were released into the solution during malachite growth but were taken up from the solution during the moolooite crystal growth phase. The shift of the molar ratio Mg/Ca was located between the two inflexion points of the crystal growth transition. This specific location at the sorption isotherm was correlated with the colour evolution by a linear discriminant model confirming its association with the polymorphs.
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ISSN: | 0969-0239 1572-882X |
DOI: | 10.1007/s10570-020-03449-3 |