Recovery of rare earths from glass polishing waste for the production of aluminium-rare earth alloys

Gerven, Tom Van; Vlugt, Thijs J. H.; Yang, Yongxiang; Spooren, Jeroen; Nielsen, Peter; Amirthalingam, Murugaiyan; Offerman, S.E.

doi:10.1016/j.resconrec.2021.105766

Cited by 16 publications

(1 citation statement)

References 22 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Cerium salts obtained in a and environmentally harmful production process are an alternative to iron and aluminium compounds but are 3-6 times more expensive [51,52]. Therefore, recovering them from industrial waste such as spent polishing powders (16,000 tons per year; [53]), spent catalysts [54,55] can contribute to a significant reduction in their prices. According to the European Commission reports from 2017-2023, Light Rare Earth Elements (LREE) recycling remains at an extremely low level of approximately 1% [56][57][58].…”

Section: Preparation Of Cerium Compoundsmentioning

confidence: 99%

Recovery of Cerium Salts from Sewage Sludge Resulting from the Coagulation of Brewery Wastewater with Recycled Cerium Coagulant

Lejwoda,

Białecka,

Barbusiński

et al. 2024

Materials

View full text Add to dashboard Cite

Due to the high cost and limited sources of cerium coagulants, it is extremely important to take measures to recycle this raw material. This paper presents the new possibility of recovering cerium(III) chloride, cerium(III) sulphate, cerium(IV) sulphate, and potentially phosphate from sewage sludge (101.5 g/kg Ce and 22.2 g/kg total P) through a brewery wastewater treatment process using recycled CeCl3 as a coagulant. In order to recover the Ce and P, the sludge was subjected to extraction using an HCl solution. Optimal process conditions were determined by means of central composite design and response surface methodology (CCD/RSM) for three input parameters (HCl mass, reaction time, and extractant volume). Under optimal conditions (0.35 g HCl per 1 g of sludge, 40 min reaction time, extractant volume of 25 mL per 1 g of sludge), the highest efficiency obtained was 99.6% and 97.5% for Ce and P, respectively. Cerium(III) oxalate as Ce2(C2O4)3∙10H2O was precipitated from the obtained solution using H2C2O4 (99.97%) and decomposed into CeO2 (at 350 °C), which was afterwards subjected to a reaction with HCl (30%, m/m) and H2O2 (30%, m/m), which led to the crystallisation of CeCl3∙7H2O with a purity of 98.6% and a yield of 97.0%. The obtained CeO2 was also subjected to a reaction with H2SO4 (96%, m/m) and H2O2 (30%, m/m), which produced Ce2(SO4)3 with a yield of 97.4%. The CeO2 was also subjected to a reaction with only H2SO4 (96%, m/m), which produced Ce(SO4)2 with a yield of 98.3%. The filtrate obtained after filtering the Ce2(C2O4)3∙10H2O contained 570 mg/L of P, which enabled its use as a source of phosphorus compounds. The presented processes of Ce and potentially P recovery from sewage sludge originating from brewery wastewater contribute to the idea of a circular economy.

show abstract