Reactivity and heavy metal removal capacity of calcium alginate beads loaded with Ca–Al layered double hydroxides

Layered double hydroxides (LDHs) present multiple applications due to their versatility and reactivity. Thus, Ca–Al LDHs with Friedel’s salt structure (HC) have been proposed as heavy metal scavengers due to their buffering capacity at basic pHs. Nevertheless, the control of the reactivity of LDHs s...

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Bibliographic Details
Authors: Borgiallo, Andres, Rojas Delgado, Ricardo
Format: article
Status:Published version
Publication Date:2019
Country:Argentina
Institution:Consejo Nacional de Investigaciones Científicas y Técnicas
Repository:CONICET Digital (CONICET)
Language:English
OAI Identifier:oai:ri.conicet.gov.ar:11336/125635
Online Access:http://hdl.handle.net/11336/125635
Access Level:Open access
Keyword:CHELATION
HYDROCALUMITE
IONIC GELATION
PH BUFFERING
PRECIPITATION
https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
Description
Summary:Layered double hydroxides (LDHs) present multiple applications due to their versatility and reactivity. Thus, Ca–Al LDHs with Friedel’s salt structure (HC) have been proposed as heavy metal scavengers due to their buffering capacity at basic pHs. Nevertheless, the control of the reactivity of LDHs such as HC is necessary to optimize their applications. Here, the reactivity of an HC prepared by a coprecipitation method was modified by its inclusion in calcium alginate (CaAlg) beads prepared by ionic gelation. The obtained beads (CaAlg/HC) showed good dispersion of the HC particles in the alginate matrix and were used to test the acid base reactivity and heavy metal uptake capacity compared with pure CaAlg beads and HC powder separately. The pH buffering capacity of CaAlg beads was enriched by the inclusion of HC that, in turn, was modulated in its reactivity. Thus, the HC dissolution times changed from mere seconds for the powder to tens of minutes when enclosed in the beads in a kinetic profile determined by the diffusive step. On the other hand, Cu2+ uptake capacity of CaAlg/HC beads combined the Cu(OH)2 precipitation capacity of HC with the complexation capacity of alginate, reaching good affinity and capacity for the obtained beads. Nevertheless, the precipitation of the hydroxide was produced outside the bead, which would induce the addition of an additional separation step to produce an acceptable Cu2+ elimination.