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TEMPLATE DESIGN © 2007 
www.PosterPresentations.com 
Preparation of Bio-diesel From Waste Oil 
Ashley White*, Bruce E. Wenzel, and Ken S. Lee 
Department of Chemistry, Jackson State University, P. O. Box 17910 
1400 J. R. Lynch Street, Jackson, MS 39217 
Abstract 
Energy crisis with higher price and 
dependency on fossil fuel has forced us to 
find alternative resources other than current 
energy system based on crude oil. It is our 
interest to find and develop cheaper energy 
resources including biomass. One example 
of current research for the alternative fuel is 
bio-diesel made from vegetable oil, like 
soybean oil. The current method uses 
vegetable oil; however, it might trigger 
several problems such as a price hike in the 
crop, which is needed for our general 
consumption. Therefore, we are interested in 
a way to make a bio-diesel from waste like 
used cooking oil. In this study we will make 
bio-diesel from cooking oil, which has been 
used in fast food restaurants and has no 
commercial value. 
Cooking oils have been used in restaurants 
were collected and used for making bio-diesel. 
The comparative study of the used oil 
and bio-diesel from various restaurants were 
made. The result of GC analysis on the fatty 
acids, various FAMEs (fatty acid methyl 
esters), glycerides in the used oil and formed 
bio-diesel product will be discussed. 
Distribution of methyl esters of saturated and 
unsaturated fatty acid (longer than C10) will 
be presented as well. 
Introduction 
Solution 
Acidity Determination 
Result of Acid Treatment with Resin 
Resin Treatment was done for 1hr. 
*72 hrs of treatment. 
Sample (5g) of WVO was mixed in 50 ml of Ethanol and it 
was titrated with standardized KOH solution. 
Bio-diesel Production 
The vegetable oil is mixed with methyl 
alcohol and converted to the methyl esters of 
fatty acids (FAME) by means of a catalyst. 
Effects of Catalysts Used on Frying Oil 
Product Cleanup 
Infrared Analysis 
Acidity calculated as mg KOH/g of sample 
Acidity=56.1 MC/W 
M: Molarity of KOH 
C: Corrected volume of KOH solution 
W: weight of Waste Veg. Oil 
1. Cool reaction mixture down. 
2. Centrifuge for 5 min. 
3. Take top layer for further treatment. 
4. Shake 3x with 10-20 ml dilute (1.0 M) HCl. 
5. Distil under vacuum. 
6. Shake with deionized water 3x or until neutral pH. 
7. Store over anhydrous MgSO4 
8. Filter. 
9.Weigh the filtrate. 
The U. S. is highly dependent on foreign 
sources of petroleum for most of its liquid 
fuels. In the second millennium, these 
sources are becoming depleted and are 
mainly in politically unstable regions. 
• Develop fuel derived from renewable, 
natural resources such as frying oil. 
Our Approach 
• Develop a process for converting natural vegetable 
oils into fuel for diesel engines. 
•Some common vegetable oils come from: soybeans, 
cottonseed, canola, peanuts, palm trees, etc. 
•Used frying oil from local restaurants: American Deli 
and Ruby Tuesday 
•High acidity of used oil has to be treated and it will be 
done with usage of resin, Dowex (MTO-Dowex M43 Anion 
Exchange Resin from SUPELCO). 
•Acidity of used oil before and after treatment with resin 
were determined. 
•Treatment of acid in used oil . Used oil was mixed with 
resin. It was stirred for 1 hour. Resin was filtered off. 
Trial 1 2 3 4 5 Avg 
Before 14.3 13.7 13.6 13.5 13.3 13.7 
After 12.6 12.7 12.7 13.3 
* 
11.6 
* 
12.7 
Reaction Conditions 
•10-100g of vegetable oil 
•10-28 ml dry methyl alcohol 
•0.1-0.9 g NaOCH3 catalyst 
•Temperature: 60°C 
•Stir vigorously 
•Reaction time: 1hr 
Weights and Volumes of Reactants 
Run Oil Weight MeOh 
(ml) 
Cat (g) 
1 Tributyrin 10 10 0.09 
2 Tributyrin 10 10 0.09 
3 Olive Oil 100 28 0.9 
4 New 
Cooking Oil 
100 28 0.9 
Chemical Reaction Example 
Catalyst Amount of 
Oil (g) 
FAME (g) Yield (%) 
NaOH 50 15.626 31.24 
NaOMe 100 43.972 43.97 
Ba(OH)2 50 27.676 55.35 
Product Yields 
Run FAME (g) Yield (%) 
1 4.05 39 
2 5.09 49 
3 82.8 82 
4 91.0 90 
Odis Lee Webb, II for his help 
Funding Sources: NIH (RCMI): G122RR13459-07S1 
NSF(STARGE):NSF-HRD-0411559 
H2C 
HC 
H2C 
O 
O 
O 
C 
O 
C 
O 
C 
O 
H2 
C 
H2 
C 
H2 
C 
H2 
C CH3 
H2 
C CH3 
H2 
C CH3 
+ CH3OH 
Catalyst 
60oC 
H3C 
O CH 
2 
H2 
C 
CH3 
O 
Trybutyrin 
Methyl butanoate (FAME) 
0 
25 
50 
75 
100 
125 
150 
175 
200 
4000 3500 3000 2500 2000 1500 1000 500 
SAMP1 
1ST BIODIESEL 
%Transmission 
Wavenumber (cm-1) 
Time (secs) FAME Area (%) 
16.82 Methyl palmitate 16.76 
18.45 Methyl linoleate 29.82 
18.50 Methyl oleate 46.93 
18.72 Methyl sterate 6.48 
GC-MS Analysis 
Acknowledgements

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Biod poster2

  • 1. TEMPLATE DESIGN © 2007 www.PosterPresentations.com Preparation of Bio-diesel From Waste Oil Ashley White*, Bruce E. Wenzel, and Ken S. Lee Department of Chemistry, Jackson State University, P. O. Box 17910 1400 J. R. Lynch Street, Jackson, MS 39217 Abstract Energy crisis with higher price and dependency on fossil fuel has forced us to find alternative resources other than current energy system based on crude oil. It is our interest to find and develop cheaper energy resources including biomass. One example of current research for the alternative fuel is bio-diesel made from vegetable oil, like soybean oil. The current method uses vegetable oil; however, it might trigger several problems such as a price hike in the crop, which is needed for our general consumption. Therefore, we are interested in a way to make a bio-diesel from waste like used cooking oil. In this study we will make bio-diesel from cooking oil, which has been used in fast food restaurants and has no commercial value. Cooking oils have been used in restaurants were collected and used for making bio-diesel. The comparative study of the used oil and bio-diesel from various restaurants were made. The result of GC analysis on the fatty acids, various FAMEs (fatty acid methyl esters), glycerides in the used oil and formed bio-diesel product will be discussed. Distribution of methyl esters of saturated and unsaturated fatty acid (longer than C10) will be presented as well. Introduction Solution Acidity Determination Result of Acid Treatment with Resin Resin Treatment was done for 1hr. *72 hrs of treatment. Sample (5g) of WVO was mixed in 50 ml of Ethanol and it was titrated with standardized KOH solution. Bio-diesel Production The vegetable oil is mixed with methyl alcohol and converted to the methyl esters of fatty acids (FAME) by means of a catalyst. Effects of Catalysts Used on Frying Oil Product Cleanup Infrared Analysis Acidity calculated as mg KOH/g of sample Acidity=56.1 MC/W M: Molarity of KOH C: Corrected volume of KOH solution W: weight of Waste Veg. Oil 1. Cool reaction mixture down. 2. Centrifuge for 5 min. 3. Take top layer for further treatment. 4. Shake 3x with 10-20 ml dilute (1.0 M) HCl. 5. Distil under vacuum. 6. Shake with deionized water 3x or until neutral pH. 7. Store over anhydrous MgSO4 8. Filter. 9.Weigh the filtrate. The U. S. is highly dependent on foreign sources of petroleum for most of its liquid fuels. In the second millennium, these sources are becoming depleted and are mainly in politically unstable regions. • Develop fuel derived from renewable, natural resources such as frying oil. Our Approach • Develop a process for converting natural vegetable oils into fuel for diesel engines. •Some common vegetable oils come from: soybeans, cottonseed, canola, peanuts, palm trees, etc. •Used frying oil from local restaurants: American Deli and Ruby Tuesday •High acidity of used oil has to be treated and it will be done with usage of resin, Dowex (MTO-Dowex M43 Anion Exchange Resin from SUPELCO). •Acidity of used oil before and after treatment with resin were determined. •Treatment of acid in used oil . Used oil was mixed with resin. It was stirred for 1 hour. Resin was filtered off. Trial 1 2 3 4 5 Avg Before 14.3 13.7 13.6 13.5 13.3 13.7 After 12.6 12.7 12.7 13.3 * 11.6 * 12.7 Reaction Conditions •10-100g of vegetable oil •10-28 ml dry methyl alcohol •0.1-0.9 g NaOCH3 catalyst •Temperature: 60°C •Stir vigorously •Reaction time: 1hr Weights and Volumes of Reactants Run Oil Weight MeOh (ml) Cat (g) 1 Tributyrin 10 10 0.09 2 Tributyrin 10 10 0.09 3 Olive Oil 100 28 0.9 4 New Cooking Oil 100 28 0.9 Chemical Reaction Example Catalyst Amount of Oil (g) FAME (g) Yield (%) NaOH 50 15.626 31.24 NaOMe 100 43.972 43.97 Ba(OH)2 50 27.676 55.35 Product Yields Run FAME (g) Yield (%) 1 4.05 39 2 5.09 49 3 82.8 82 4 91.0 90 Odis Lee Webb, II for his help Funding Sources: NIH (RCMI): G122RR13459-07S1 NSF(STARGE):NSF-HRD-0411559 H2C HC H2C O O O C O C O C O H2 C H2 C H2 C H2 C CH3 H2 C CH3 H2 C CH3 + CH3OH Catalyst 60oC H3C O CH 2 H2 C CH3 O Trybutyrin Methyl butanoate (FAME) 0 25 50 75 100 125 150 175 200 4000 3500 3000 2500 2000 1500 1000 500 SAMP1 1ST BIODIESEL %Transmission Wavenumber (cm-1) Time (secs) FAME Area (%) 16.82 Methyl palmitate 16.76 18.45 Methyl linoleate 29.82 18.50 Methyl oleate 46.93 18.72 Methyl sterate 6.48 GC-MS Analysis Acknowledgements