TRACING/DEVELOPMENT OF CATALYSTS FOR REDOX REACTION OF METHYL LINOLEATE (BIODIESEL) WITH GLYCEROL
Thermodynamic calculations showed that the following transfer hydrogenation reaction with glycerol as hydrogen donor ???????????????????????????????????????????????? ???? ???? ??????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????...
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Main Author: | |
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Format: | Final Project |
Language: | Indonesia |
Subjects: | |
Online Access: | https://digilib.itb.ac.id/gdl/view/66487 |
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Institution: | Institut Teknologi Bandung |
Language: | Indonesia |
Summary: | Thermodynamic calculations showed that the following transfer hydrogenation reaction
with glycerol as hydrogen donor
???????????????????????????????????????????????? ???? ???? ???????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????? ???? ???? ????????????????????????????????????????????????????????
methyl linoleate glycerol methyl oleate dihydroxyacetone
will be able to proceed to the right with a complete conversion even at room temperature,
provided a suitable catalyst is available. Thus, if such a catalyst could be found then a
process with high commercial value could be established : methyl linoleate will be
hydrogenated into methyl oleate and, at the same time, glycerol will be dehydrogenated
into a higher added-value product, that is dihydroxyacetone. Further literature study
revealed that compounds (Ni½Zn½)(OOCH)2.2H2O, Ni(CrIII)2O (OOCH)6.3H2O, and
Ni(FeIII)2O(OOCH)6.3H2O are potential candidates to become the catalyst for the above
redox reaction between methyl linoleate and glycerol.
The objective of the research proposed here is to obtain experiments-based
prove/disprove on the hypothesis of effectivity of the catalysts candidates and to further
explore the exact operating conditions for the catalyst candidates that are proven to be the
most effective. The experimental examinations will be carried out by adding the catalyst
into solution of biodiesel, glycerol, and acetone with the addition of DMSO (if the catalyst
was not an imidazole complex) which was then reacted at a reaction temperature (= 40 °C)
and at the reflux temperature of the reaction mixture (about 56 °C) for 6 hours. The
biodiesel resulting from the reaction under reflux conditions was then analyzed for iodine
value, peroxide value and its oxidation stability through the rancimat test.
Based on the experiment, among the catalyst candidates tested, none of the catalysts
proved effective for carrying out a redox reaction (catalytic hydrogenation-transfer) at a
relatively low temperature (<100 °C) for 6 hours |
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