4.7 Article

Microwave acid baking process for recovery of rare-earth concentrate from phosphor of end-of-life fluorescent lamps

Journal

JOURNAL OF CLEANER PRODUCTION
Volume 307, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.jclepro.2021.127235

Keywords

Fluorescent lamps; Phosphor; Recycling; Baking; Activation energy; Microwave

Funding

  1. Indian Institute of Technology, Roorkee, India [FIG-100714]

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A novel processing route involving microwave-assisted acid baking and water leaching was explored for recycling waste phosphor from end-of-life fluorescent lamps. Various parameters were optimized, and the process showed high efficiency in rare-earth dissolution. Additionally, cost estimations indicated economic viability with significant contribution from terbium.
A novel processing route of microwave-assisted acid baking followed by water leaching of waste phosphor retrieved from end-of-life fluorescent lamps is investigated. The waste phosphor consists of a mixture of monochromatic phosphor phases (Y2O3:Eu3+, BaMgAl10O17:Eu2+, CeMgAl11O19:Tb3+, LaPO4:Ce3+Tb3+), and the baking parameters like microwave power, baking duration, and acid dose were optimized using randomized block statistical design of experiments. The thermodynamic considerations of the sulfation process are evaluated by the thermogravimetric analysis of the phosphor-acid mixture. The estimated thermal decomposition activation energies for the predicted sulfation reactions are 652.9, 375.9, and 409.5 kJ/mol at 0.7, 0.85, and 1 mL/g acid dosage, respectively, in the temperature range of 231-308 degrees C. It was found that the microwave baking at 800 W for 3 min at 1 mL/g acid ratio yielded 82.5% overall rare-earth dissolution, including 93.6% terbium, 39.6% lanthanum, and similar to 100% europium and yttrium dissolution. Cerium dissolution was negligible in the investigated experimental conditions. The dissociation of the LaPO4:Ce3+Tb3+ phase governs the overall rare earth dissolution during the baking process. The XRD analysis of the products suggests that the lanthanum and cerium values interact with phosphoric acid at the phosphor surface to form polyphosphates (LaPO4, CePO4), deteriorates the dissolution efficiency. The partially reacted Ce (III) values were oxidized to a stable Ce (IV) state, which leads to its accumulation in the leach residue. The mass balance at optimal conditions indicates that 184 g phosphor of 100 tubular lights units yielded 73 g of 98% pure Y-Eu-Tb oxides. The specific energy expenditure for the present lab-scale study was calculated at 8 kWh/kg of phosphor. The cost estimations indicate that the process is economically viable with a total value generation of 14.47 US$/kg with 89% contribution of terbium and cost of processing is 0.69 US$/Kg phosphor.

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