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Microwave-driven oleic acid esterification over chlorosulfonic acid-treated hydroxyapatite: synergism for intensified biodiesel production

Treating hydroxyapatite (HAP) with sulfonic acid without structural destruction remains challenging owing to the sensitivity of HAP to acidic pH. In this work, natural derived HAP was prepared using natural phosphate via a dissolution/precipitation process. Notwithstanding the challenge, the prepare...

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Bibliographic Details
Published in:RSC advances 2024-10, Vol.14 (45), p.3319-3333
Main Authors: Rezki, Boutaina, Essamlali, Younes, Amadine, Othmane, Sair, Said, Aadil, Mina, Zahouily, Mohamed
Format: Article
Language:English
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Summary:Treating hydroxyapatite (HAP) with sulfonic acid without structural destruction remains challenging owing to the sensitivity of HAP to acidic pH. In this work, natural derived HAP was prepared using natural phosphate via a dissolution/precipitation process. Notwithstanding the challenge, the prepared HAP was treated with three concentrations of chlorosulfonic acid in dichloromethane to prepare HAP-S1, HAP-S2 and HAP-S3 depending on the acid content under carefully controlled conditions. The treatment of HAP with the lowest acid concentration led to the preservation of the apatite framework with surface modification of sulfonic acid groups. As the acid concentration increased, HAP, CaHPO 4 and CaSO 4 were obtained. A further increase in the acid concentration led to the formation of CaSO 4 with the coexistence of Ca(H 2 PO 4 ) 2 ·H 2 O. Subsequently, the catalytic activity of HAP-S1 was evaluated in oleic acid esterification under microwave irradiation, resulting in a yield of up to 87% under optimized conditions of 10 wt% of catalyst to oleic acid weight, 10 : 1 methanol to oleic acid molar ratio, and 40 min reaction duration under microwave irradiation at 150 °C. The activity of HAP-S1 was attributed to the active S&z.dbd;O and S-O-H functional groups, and a possible mechanism of acid-catalyzed esterification is proposed. The catalyst was also tested in the transesterification reaction of rapeseed oil, achieving a conversion of 40.2% after 60 min reaction duration under microwave irradiation. Furthermore, the catalyst was evaluated in a two-step esterification reaction to investigate its activity towards acidified feedstocks. Results showed that after two successive runs, acidity was reduced by 79.6% with a total FAME yield of 40.13%. The obtained results indicate that this catalyst, being an acid catalyst, is more suitable for direct esterification. Microwave-assisted oleic acid esterification to methyl oleate using a sulfonated natural-hydroxyapatite catalyst: an efficient process for biodiesel production using a natural phosphate-derived acid catalyst.
ISSN:2046-2069
2046-2069
DOI:10.1039/d4ra05862c