کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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204896 | 461093 | 2016 | 9 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Highly selective acetalization of glycerol with acetone to solketal over acidic carbon-based catalysts from biodiesel waste Highly selective acetalization of glycerol with acetone to solketal over acidic carbon-based catalysts from biodiesel waste](/preview/png/204896.png)
• Green carbon-based solid with high catalytic activity in the glycerol acetalization reaction.
• High selectivity of solketal products of the acetalization reaction.
• Carbon-based acid preparation: an efficient approach for the valorization of a biodiesel waste, glycerin.
• High stability of the acid group surfaces present on the carbon-based catalyst surface.
The glycerol acetalization reaction in the presence of acetone was evaluated using acidic carbon-based catalysts from biodiesel waste as catalysts. Acidic carbon-based catalysts were prepared with different glycerin:sulfuric acid mass ratios at 457 K for 24 h. The amount of acid groups as well as the acidity (mainly attributed to sulfur groups) enhance with an increase of glycerol:sulfuric acid ratio (1:2 and 1:3, named GC-1:2 and GC-1:3, respectively), reaching 0.9 mmol g−1 for sulfur and 3.8 mmol g−1 for total acidity. Very promising results were obtained when these carbon-based catalysts were tested as catalysts in glycerol acetalization, reaching about 80% of glycerol conversion and about 95% of solketal selectivity, this product has been applied as a fuel additive. Furthermore, the carbon-based catalysts surface groups showed high stability under the reaction conditions tested in this study. These results indicated that acidic carbon-based catalysts derived from glycerin are very attractive catalysts for glycerol acetalization.
Biodisel production byproduct (glycerol) is transformed in a environmental acid carbon which is used as catalyst in glycerol acetalization.Figure optionsDownload as PowerPoint slide
Journal: Fuel - Volume 181, 1 October 2016, Pages 46–54