Residual Na, K, Mg, and Ca in crystallized aluminum chloride limit alumina purity during recovery from coal fly ash. This study investigated a purification route combining low-temperature thermal decomposition (250–450 °C), stepwise leaching (single-step leaching tests: 60–160 °C), and final calcination (950 °C). Steam enhanced dechlorination compared with argon. At comparable mass loss and residual chlorine levels, treatment at 350 °C for 360 min favored subsequent Mg and Ca removal over treatment at 400 °C for 240 min. The former yielded alumina containing 150 ppm MgO and 182 ppm CaO after leaching and calcination. K and Ca were readily removed under mild conditions, whereas Mg removal benefited from longer leaching times. Structural rearrangement during boehmite formation may facilitate impurity release. Two-step leaching with dilute hydrochloric acid, initially adjusted to pH 4, improved Mg removal. After calcination, alumina purity reached 99.73%, compared with 95.44% for the control. Simulated leachate reuse showed greater sensitivity of Mg removal to impurity accumulation. An experiment using 10 kg of aluminum chloride hexahydrate achieved removal efficiencies above 99.4% for Na, K, and Ca and 98.02% for Mg, with 95.29% Al recovery. These results support thermal decomposition coupled with stepwise leaching for selective impurity removal while retaining Al.
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Zheng et al. (2026) studied this question.
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