2020
DOI: 10.1016/j.micromeso.2019.109856
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Use of pinene as a solvent for the synthesis of aluminophosphate and its application in the hydrogenation of pinene

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Cited by 3 publications
(6 citation statements)
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“…The support APO‐PT (pinene‐thermal‐synthesized aluminophosphate) was prepared following the procedure given in the reference 21 . Briefly, 3.9 g of Al(OH) 3 (Al source), 5.8 g of H 3 PO 4 (P source), and 5.6 g of triethylamine (TEA, structure‐directing agent) were added into 50 g of α‐pinene (solvent) and stirred for 4 h. The obtained gel was placed into a PTFE‐lined autoclave (100 mL) for crystallization at 453 K for 36 h. Subsequently, the crystallization product was filtered, washed, dried at 383 K for 24 h, and then calcined in a muffle at 773 K for 5 h. The product was used as the catalyst support.…”
Section: Methodsmentioning
confidence: 99%
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“…The support APO‐PT (pinene‐thermal‐synthesized aluminophosphate) was prepared following the procedure given in the reference 21 . Briefly, 3.9 g of Al(OH) 3 (Al source), 5.8 g of H 3 PO 4 (P source), and 5.6 g of triethylamine (TEA, structure‐directing agent) were added into 50 g of α‐pinene (solvent) and stirred for 4 h. The obtained gel was placed into a PTFE‐lined autoclave (100 mL) for crystallization at 453 K for 36 h. Subsequently, the crystallization product was filtered, washed, dried at 383 K for 24 h, and then calcined in a muffle at 773 K for 5 h. The product was used as the catalyst support.…”
Section: Methodsmentioning
confidence: 99%
“…The support APO-PT (pinene-thermal-synthesized aluminophosphate) was prepared following the procedure given in the reference. 21 Briefly, 3.9 g of Al(OH) 3 (Al source), 5.8 g of H 3 PO 4 (P source), and 5.6 g of triethylamine (TEA, structure-directing agent) were added into 50 g of α-pinene (solvent) and stirred for 4 h. The obtained gel was placed into a PTFE-lined autoclave (100 mL) for crystallization at 453 K for 36 h. Subsequently, the crystallization product was filtered, washed, dried at 383 K for 24 h, and then calcined in a muffle at 773 K for 5 h. The product was used as the catalyst support. The catalyst Ni/APO-PT was prepared as follows: 1.5 g of APO-PT was added into a 10 mL nickel nitrate solution, where the Ni ion concentration was 10 wt% under ultrasonic vibration for 1 h. Then, the solvent was evaporated under an infrared lamp, and the remaining solid powder (Ni(NO 3 ) 2 /APO-PT) was calcined at 723 K for 3 h in a muffle.…”
Section: Preparation Of the Ni/apo-pt Catalystmentioning
confidence: 99%
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