2014
DOI: 10.1039/c4cy00714j
|View full text |Cite
|
Sign up to set email alerts
|

Selective glycerol transformations to high value-added products catalysed by aluminosilicate-supported iron oxide nanoparticles

Abstract: Conversion of glycerol to cyclic acetals (with paraformaldehyde, benzaldehyde, furfural and acetone) and to mono-, di-and triacetylglycerides (with levulinic acid) was investigated using a supported iron oxide nanoparticle system of a mesoporous aluminosilicate heterogeneous catalyst (Fe/Al-SBA-15). The effect of various parameters on the reaction, temperature, mol% of catalyst or ratio of glycerol : substrate were studied. An optimization of the reaction conditions carried out with glycerol by means of experi… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

3
39
0

Year Published

2015
2015
2023
2023

Publication Types

Select...
7

Relationship

1
6

Authors

Journals

citations
Cited by 54 publications
(44 citation statements)
references
References 41 publications
(35 reference statements)
3
39
0
Order By: Relevance
“…When the resultant catalyst was tested in the esterification of glycerol with acetic acid, the mesoporous support with 15 wt% MPA exhibited a superior catalytic activity with complete conversion of glycerol (100%) with a selectivity of 14%, 67% and 19% towards mono-, di-and triacetin at 110 • C, 6:1 molar ratio of acetic acid to glycerol in 3 h. The catalyst was recycled four times and was found to be stable. The use of supported iron oxide nanoparticle system of a mesoporous aluminosilicate (Fe/Al-SBA-15) catalyst with >99% glycerol conversion to a mixture of 71% di-and 28% triacetin was reported [121]. Though levulinic acid was used as against the conventional acetic acid but the catalyst remains stable even after five consecutive cycles.…”
Section: Acetin (Glycerol Esters)mentioning
confidence: 99%
See 1 more Smart Citation
“…When the resultant catalyst was tested in the esterification of glycerol with acetic acid, the mesoporous support with 15 wt% MPA exhibited a superior catalytic activity with complete conversion of glycerol (100%) with a selectivity of 14%, 67% and 19% towards mono-, di-and triacetin at 110 • C, 6:1 molar ratio of acetic acid to glycerol in 3 h. The catalyst was recycled four times and was found to be stable. The use of supported iron oxide nanoparticle system of a mesoporous aluminosilicate (Fe/Al-SBA-15) catalyst with >99% glycerol conversion to a mixture of 71% di-and 28% triacetin was reported [121]. Though levulinic acid was used as against the conventional acetic acid but the catalyst remains stable even after five consecutive cycles.…”
Section: Acetin (Glycerol Esters)mentioning
confidence: 99%
“…The use of supported iron oxide nanoparticle system of a mesoporous aluminosilicate heterogeneous catalyst (Fe/Al-SBA-15) in acetalization of glycerol with paraformaldehyde, benzaldehyde, furfural and acetone was investigated at 100 • C [121]. All the reactions gave very good conversion and selectivity to glycerol formal.…”
Section: Acetalmentioning
confidence: 99%
“…Glycerol has a large number of applications in the pharmaceutical, cosmetic, and food industries [5,6]. Currently, chemical efforts focus on finding new uses for glycerol to output large surplus produced by industry and turn it into products with high added value [7,8] The catalytic transformation of glycerol into various chemicals by hydrogenolysis [9,10], polymerization [11] etherification [12,13], oxidation [14], dehydration [15,16], esterification [17] and acetalysation [18], among other, has been reported.…”
Section: Introductionmentioning
confidence: 99%
“…The use of solid acids, such as supported heteropoly acids having high catalytic efficiency, results in high solubility in polar media and hence there is difficulty in separation from the reaction medium. [22] The main drawback of sulphated zirconia is that it is prone to deactivation after one reaction usage due to the formation of coke precursors. Ionic liquids suffer from drawbacks such as toxicity during their preparation, high cost and their disposal after reaction.…”
Section: Introductionmentioning
confidence: 99%