TY - JOUR
T1 - Selective adsorption of gadolinium from real leachate using a natural bentonite clay
AU - Dotto, Guilherme L.
AU - Vieillard, Julien
AU - Pinto, Diana
AU - Lütke, Sabrina F.
AU - Silva, Luis F.O.
AU - dos Reis, Glaydson S.
AU - Lima, Éder C.
AU - Franco, Dison S.P.
N1 - Publisher Copyright:
© 2023 Elsevier Ltd
PY - 2023/6
Y1 - 2023/6
N2 - This article investigated the recovery of Gd3+ from real leachate of phosphogypsum (PG) using natural bentonite clay. Firstly, a detailed adsorption study was performed using synthetic Gd3+ solutions. Then, it was investigated the clay performance in the real PG leachate. The characterization results indicate classical bentonite characteristics, such as rugosity and an SBET 91.3 m² g−1, with meso (Dp =3.82 nm) and macroporous (Dp =52.6 nm). In addition, it was identified that the major functional groups are hydroxyl and silicate, with the presence of organic matter. The initial pH solution effect indicates that the optimum removal of Gd3+ is at pH (6), attributing to the pHpzc being at 5.75 and the negatively charged surface above the pHpzc. The Avrami fractional order model was the most suitable for describing the experimental kinetic data. The Langmuir was the proper model for describing the adsorption isotherms, indicating that the Gd3+ forms a monolayer at the surface of the bentonite. The maximum adsorption capacity at pH 6.0 was 121.5 mg g−1. The thermodynamic parameters indicate that the adsorption is spontaneous, with a standard enthalpy change of − 92.30 kJ mol−1, indicating an ionic exchange, where the Gd3+ tends to be organized at the surface, according to the standard entropy change of − 206.0 J K−1 mol−1. The fixed bed adsorption test showed that Gd3+ could be adsorbed for up to 200 min without regeneration. Regeneration results show that the citric acid is more efficient in desorbing the Gd3+ from the bentonite, reaching up to 8 cycles without efficiency loss. Finally, the bentonite clay could selectively recover Gd3+ from the real PG leachate.
AB - This article investigated the recovery of Gd3+ from real leachate of phosphogypsum (PG) using natural bentonite clay. Firstly, a detailed adsorption study was performed using synthetic Gd3+ solutions. Then, it was investigated the clay performance in the real PG leachate. The characterization results indicate classical bentonite characteristics, such as rugosity and an SBET 91.3 m² g−1, with meso (Dp =3.82 nm) and macroporous (Dp =52.6 nm). In addition, it was identified that the major functional groups are hydroxyl and silicate, with the presence of organic matter. The initial pH solution effect indicates that the optimum removal of Gd3+ is at pH (6), attributing to the pHpzc being at 5.75 and the negatively charged surface above the pHpzc. The Avrami fractional order model was the most suitable for describing the experimental kinetic data. The Langmuir was the proper model for describing the adsorption isotherms, indicating that the Gd3+ forms a monolayer at the surface of the bentonite. The maximum adsorption capacity at pH 6.0 was 121.5 mg g−1. The thermodynamic parameters indicate that the adsorption is spontaneous, with a standard enthalpy change of − 92.30 kJ mol−1, indicating an ionic exchange, where the Gd3+ tends to be organized at the surface, according to the standard entropy change of − 206.0 J K−1 mol−1. The fixed bed adsorption test showed that Gd3+ could be adsorbed for up to 200 min without regeneration. Regeneration results show that the citric acid is more efficient in desorbing the Gd3+ from the bentonite, reaching up to 8 cycles without efficiency loss. Finally, the bentonite clay could selectively recover Gd3+ from the real PG leachate.
KW - Adsorption
KW - Gadolinium
KW - Kinetics
KW - Natural clay
KW - Selectivity
KW - Thermodynamics
UR - http://www.scopus.com/inward/record.url?scp=85151435461&partnerID=8YFLogxK
U2 - 10.1016/j.jece.2023.109748
DO - 10.1016/j.jece.2023.109748
M3 - Article
AN - SCOPUS:85151435461
SN - 2213-3437
VL - 11
JO - Journal of Environmental Chemical Engineering
JF - Journal of Environmental Chemical Engineering
IS - 3
M1 - 109748
ER -