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dc.contributor.authorYang, Jeremy
dc.contributor.authorBurra, Kiran
dc.contributor.authorCorrell-Brown, Riordan
dc.contributor.authorZhou, Christine
dc.contributor.authorLiu, Xinan
dc.contributor.authorGupta, Ashwani
dc.date.accessioned2026-08-23T07:44:31Z
dc.date.available2026-08-23T07:44:31Z
dc.date.copyright2026/06/01
dc.date.issued2026
dc.identifier.issn2997-0253
dc.identifier.otherjerta-26-1065.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4315530
dc.description.abstractAbstract. The expansion of solar energy has intensified concerns about the end-of-life management of solar panels. High-purity constituent materials can be recovered through chemical delamination, but conventional solvents such as toluene acid and nitric acid and hydrofluoric acids pose substantial environmental and health risks. We evaluate d-limonene, a biodegradable green solvent, for solar panel recycling by investigating its interaction with ethylene–vinyl acetate (EVA), the critical encapsulant layer in solar panels. This study focused on the dissolution and swelling kinetics of EVA samples with varying degrees of cross-linking in d-limonene. Results showed that the EVA dissolution behavior strongly depends on its degree of cross-linking. Linear EVA beads readily dissolved within 2.5 h at room temperature, whereas lightly cross-linked EVA films required elevated temperatures (∼70 °C) for dissolution. The highly cross-linked EVA used in commercial solar panels remained insoluble even at 70 °C, but exhibited substantial swelling. The swelling kinetics showed a linear relationship between the reciprocal swelling rate and time, indicating dominance by stress relaxation in the cross-linked structure. The swelling ratio reached approximately 2 after 90 min at room temperature. At 70 °C, the initial swelling rate increased by approximately sixfold, while the maximum swelling ratio increased marginally. This temperature-accelerated swelling enabled effective delamination and separation of solar panel fragments. Fourier transform infrared spectroscopy showed that characteristic peaks of filtered d-limonene after delamination were identical to those of pristine d-limonene, indicating negligible byproduct formation and allowing solvent reuse after simple filtration.
dc.publisherThe American Society of Mechanical Engineers (ASME)
dc.titleEvaluating the Green Solvent d-Limonene for Sustainable Chemical Delamination in Solar Panel Recycling
dc.typeJournal Paper
dc.journal.volume2
dc.journal.issue6
dc.journal.titleJournal of Energy Resources Technology, Part A: Sustainable and Renewable Energy
dc.identifier.doi10.1115/1.4071511
dc.treeJournal of Energy Resources Technology, Part A: Sustainable and Renewable Energy:;2026:;volume( 002 ):;issue:006
dc.contenttypeFulltext


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