کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
204948 | 461093 | 2016 | 10 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Kinetics of ethylic esterification of lauric acid on acid activated montmorillonite (STx1-b) as catalyst Kinetics of ethylic esterification of lauric acid on acid activated montmorillonite (STx1-b) as catalyst](/preview/png/204948.png)
• We used an acid activated montmorillonite as catalyst to fatty acid esterification with ethanol.
• High fatty acid conversions were observed.
• Eley–Rideal mechanism was successfully used to describe the kinetic reaction.
• The catalyst showed activity after reuse cycles.
This work reports a kinetic study of catalyzed esterification of lauric acid with anhydrous ethanol related to biodiesel production. The catalyst consists of a clay mineral (montmorillonite STx1-b) prepared according to procedure previously described in literature. The acid activation was confirmed by X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). Operating parameters: temperature (T = 140 and 180 °C), molar ratio ethanol to lauric acid (MR = 6:1 and 12:1) and catalyst loading (CAT = 2 and 10 wt%, in relation to the fatty acid mass) were evaluated as a preliminary study to the kinetics. Temperature is clearly the factor that most contributes to higher conversions of fatty acid, however, its effect was less pronounced with the use of the catalyst. Moreover, reaction kinetic experiments were performed at different conditions (T = 140, 160 and 180 °C; MR = 3:1, 6:1 and 9:1, CAT = 0, 10 and 20 wt%) as well as kinetics modeling are presented. The Eley–Rideal mechanism with surface reaction between adsorbed ethanol and lauric acid in the bulk as the limiting step was proposed to represent the catalyzed reactions, in which the global reaction rate was expressed as the sum of non-catalyzed (thermal conversion) and catalyzed reactions. From the results presented, it can be seen that the catalyst montmorillonite STx1-b was able to lead the system to high conversions in shorter time when compared to the non-catalyzed reaction.
Journal: Fuel - Volume 181, 1 October 2016, Pages 600–609