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The effect agitation on the leaching efficiency of REE from bauxite residue in 1.5 M H2SO4 at 90 °C (with and without microwave pretreatment) within 30 min residence time. The dashed lines represent the maximum leaching efficiency that could be achieved using 3 M HNO3 at 90 °C without microwave pretreatment. Error bars represent the standard error of the mean for four replicates.

The effect agitation on the leaching efficiency of REE from bauxite residue in 1.5 M H2SO4 at 90 °C (with and without microwave pretreatment) within 30 min residence time. The dashed lines represent the maximum leaching efficiency that could be achieved using 3 M HNO3 at 90 °C without microwave pretreatment. Error bars represent the standard error of the mean for four replicates.

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Some rare earth elements (REEs) are classified under critical materials, i.e., essential in use and subject to supply risk, due to their increasing demand, monopolistic supply, and environmentally unsustainable and expensive mining practices. To tackle the REE supply challenge, new initiatives have been started focusing on their extraction from alt...

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... Under atmospheric circumstances, a single acid could not entirely dissolve red dirt, according to this study. Reid et al. (2017) examined the REEs' leaching from red mud from Canada under atmospheric pressure using various acids. For 30 min, HCl, HNO 3 , and H 2 SO 4 were employed at varied leaching settings with concentration of acids ranging from 0.5 to 3 mol/L and temperature ranging from 25°-90°C. ...
... The kinetic modeling of nickel leaching from the spent catalyst was carried out within 6 h, and four models were evaluated based on a literature review for leaching: [30][31][32][33][34] (1) diffusion control through the fluid film (Eq 2); (2) solid product diffusion control (Eq 3); (3) surface chemical reaction control (Eq 4); and (4) porous product layer (Eq 5). In the equations, k 1 , k 2 , k 3 , and k 4 (h À1 ) are the rate constants, t is the time reaction (min), and x is the fractional conversion of nickel. ...
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... Since the kinetic behavior presented for almost all REE was very similar ( Fig. 4 and 5), the leaching mechanism was investigated only for the sum of all REE. For the fitting, the experimental data obtained up to 10 min for the US-assisted leaching and up to 20 min for leaching at silent condition, that is, the experimental data obtained up to the time required for each system to approach equilibrium, were considered [46,47]. The results obtained from the shrinking core model fitting are shown in Fig. 6. ...
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... The by-product obtained is red mud or bauxite residue. It is then washed to recover caustic soda and then dumped off (Reid et al., 2017;Samal et al., 2013). A schematic representation of the Bayer process has been depicted in Fig. 1. ...
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... Table 1 presents the Sc concentration in different Bauxite Residues worldwide as reported in literature. (Reid et al., 2017) It has been estimated that 70% of the world's Sc resources might be found in bauxite minerals and bauxite residue (Petrakova et al., 2016). Scandium is a very rarely concentrated element, making commercially usable deposits of this critical material very rare. ...
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... The PG morphology had a nonlinear progression with microwave irradiation time, which was due to the factor that the drying rate of microwaved gypsum depended primarily on the particle moisture content (a nonlinear trend) and the microwave power [69]. It was observed that, as the microwave irradiation duration increased, the PG morphology had changed gradually, resulting in increased surface roughness and particle porosity [68]. In contrast, there were no morphological changes when the PG samples were heated in a conventional oven at 100 or 150 • C. The research of Yang et al. [70] had shown that microwave irradiation could induce the formation of CaSO 4 ·0.5H 2 O, which required temperatures exceeding 107 • C, by creating localized hot spots. ...
... In the study of Lindroth et al., when a sample of wet gypsum was exposed to 1400 W for 2 min, a small amount of CaSO 4 ·0.5H 2 O was produced, with no CaSO 4 production [71]. In the study of Adrian Lambert et al. [68], as the microwave power and duration was increased, there was a sharp drop in CaSO 4 ·2H 2 O content, accompanied by a proportional increase in CaSO 4 ·0.5H 2 O and CaSO 4 . Thus, it could be seen that microwave heating and irradiation caused a distinct change in the crystal structure of the PG sample, causing a shift from the doubly hydrated gypsum to hemihydrated gypsum to anhydrous gypsum. ...
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