Surfactant-assisted synthesis of MgO: Characterization and catalytic activity on the transesterification of dimethyl carbonate with glycerol
- Authors
- Simanjuntak, Fidelis Stefanus Hubertson; Lim, Seung Rok; Ahn, Byoung Sung; Kim, Hoon Sik; Lee, Hyunjoo
- Issue Date
- 2014-08-22
- Publisher
- ELSEVIER SCIENCE BV
- Citation
- APPLIED CATALYSIS A-GENERAL, v.484, pp.33 - 38
- Abstract
- Various forms of MgO were synthesized and used as catalysts in the transesterification of dimethyl carbonate (DMC) with glycerol for the synthesis of glycerol carbonate (GLC). MgO synthesized using a surfactant (a triblock copolymer of ethylene oxide/propylene oxide/ethylene oxide, known as Pluronic F127) showed a much higher GLC yield of 75.4% compared to other MgO catalysts synthesized without using a surfactant at reaction conditions of 90 degrees C, DMC/glycerol = 2, and catalyst/glycerol = 5 wt%. With an increase of the weight ratio of the surfactant/Mg precursor, the catalytic activity was increased. However, the activity did not change substantially when the surfactant/Mg precursor ratio was greater than 5. The high catalytic activity of MgO prepared with the surfactant (MgO-S) is attributed to the higher basic site concentration on the surface. This originated from low-coordination oxide ions at the corner sites (O-3c(2-)), as shown in the basic site titration and UV-diffuse reflectance analysis results. It is also noted that MgO-S could be easily recovered after the reaction and reused at least five times without serious catalyst deactivation. (C) 2014 Elsevier B.V. All rights reserved.
- Keywords
- MAGNESIUM-OXIDE; NANOCRYSTALLINE MGO; INORGANIC MATERIALS; HYDROXIDE; SIZE; NANOSTRUCTURES; BIODIESEL; MAGNESIUM-OXIDE; NANOCRYSTALLINE MGO; INORGANIC MATERIALS; HYDROXIDE; SIZE; NANOSTRUCTURES; BIODIESEL; Glycerol; Dimethyl carbonate; Glycerol carbonate; Magnesium oxide; Surfactant
- ISSN
- 0926-860X
- URI
- https://pubs.kist.re.kr/handle/201004/126451
- DOI
- 10.1016/j.apcata.2014.06.028
- Appears in Collections:
- KIST Article > 2014
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