Transesterification of waste cooking oil using clinoptilolite/ industrial phosphoric waste as green and environmental catalysts
This paper focuses on creating a new, environmentally sustainable catalyst made of industrial phosphoric waste and clinoptilolite for transesterification of waste cooking oil. A state-of-the-art CaO-based catalyst supported on the industrial phosphoric waste was obtained from a clinoptilolite zeolit...
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Veröffentlicht in: | Energy (Oxford) 2022-04, Vol.244, p.123138, Article 123138 |
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Sprache: | eng |
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Zusammenfassung: | This paper focuses on creating a new, environmentally sustainable catalyst made of industrial phosphoric waste and clinoptilolite for transesterification of waste cooking oil. A state-of-the-art CaO-based catalyst supported on the industrial phosphoric waste was obtained from a clinoptilolite zeolite-like material and alkali-activated CaO. So after ordinary purification, the clinoptilolite, and the weighed calcium oxide were stirred for 24 h at room temperature and then kept at 800 °C for 2 h for the formation of the catalyst. For assessment of the catalyst, the study used XRF, FT-IR, SEM, XRD, and BET. Under optimized conditions, the highest purity of biodiesel for waste cooking oil was 84.76%, the oil to methanol volume ratio was 1.47, the catalyst dosage was 8.08 wt%, the temperature was 54.72 °C, and the duration was 119 min. Results indicated that using waste cooking oil as raw materials and clinoptilolite/CaO as a catalyst for biodiesel development is a cost-effective and eco-friendly oil-recycling method and minimizes the production costs of biodiesel to improve biodiesel's competitiveness vis petroleum diesel.
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•The study presented a novel catalyst from industrial phosphoric waste/Clinoptilolite.•The variables of the transesterification process were optimized using RSM.•BET, XRF, SEM, FT-IR, and XRD were used for characterizing the synthesis catalyst.•Under optimum conditions, the FAME content of 84.76% was obtained over 119 min. |
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ISSN: | 0360-5442 1873-6785 |
DOI: | 10.1016/j.energy.2022.123138 |