2018
DOI: 10.1016/j.fuel.2018.06.121
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Transesterification of non-edible oils over potassium acetate impregnated CaO solid base catalyst

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Cited by 60 publications
(21 citation statements)
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“…The diffraction lines at 18.2° and 34.2° indicate the existence of Ca(OH) 2 in a certain amount, which could be due to the water absorption of CaO. The characteristic diffraction lines of CaCO 3 appeared in 23.4°, 36.2°, and 39.3°, which may be formed by the reaction of CaO and CO 2 during calcination [30]. The diffraction line at 27.9° showed the presence of B 2 O 3 [23].…”
Section: Resultsmentioning
confidence: 99%
“…The diffraction lines at 18.2° and 34.2° indicate the existence of Ca(OH) 2 in a certain amount, which could be due to the water absorption of CaO. The characteristic diffraction lines of CaCO 3 appeared in 23.4°, 36.2°, and 39.3°, which may be formed by the reaction of CaO and CO 2 during calcination [30]. The diffraction line at 27.9° showed the presence of B 2 O 3 [23].…”
Section: Resultsmentioning
confidence: 99%
“…By comparing with other CaO modified catalyst reports, the niobium/calcium oxides mix display higher conversion respect to Ca/Mg, 24 Ca/Ce 30 catalysts, similar values when compared with PA/CaO 29 and CaO/CuFe 2 O 4 31 catalysts, and lower conversion when relates with the yield performane of catalyst as Ca:Zn, 22,23 Sr 2+ -CaO/MgO, 25 CaO-MgO, 26 KF/CaO, 28 and CaO-CeO 2 . 32 Considering that the optimal temperature is higher than the boiling point of methanol, which cause the loss of reactant by vaporization, this can influence the results on the optimization of the molar ratio, which is higher compared with other reports [22][23][24][25][26][27][28][29][30][31][32] for CaO catalysts (1:9 to 1:30). About other aspects like reaction time (2 to 6 h) and mass amount of catalyst (2 to 5 wt.%) our results are in the range.…”
Section: Resultsmentioning
confidence: 89%
“…Using potassium acetate (PA) to prepare PA/CaO solid base catalyst, Fadhil et al 29 tested two non-edible oils, using 9:1 methanol to oil molar ratio, at 60 °C, 120 min, and obtaining a maximum conversion of 93%.…”
Section: Introductionmentioning
confidence: 99%
“…The weak vibration of M+-O stretching adsorption bands at 544.80 cm −1 , and 463.04 cm −1 belonged to Fe-O and K-O bonding, respectively [62].The deformation bands of M + -OH converted to Si-O-M + located at 964.71 cm −1 and 912.26 cm −1 were assigned to Fe and K, respectively [63]. Upon the formation of Si-O-M + , the intensity of the siloxane absorption band was reduced and shifted to lower frequency due to the reduction of electron density [64].…”
Section: Functional Group Analysismentioning
confidence: 99%