Sunday, October 13, 2013

Biofuels

Part 1: Synthesizing Biofuel

In this practical, we attempted to synthesize biofuel using corn oil. Corn oil is a triglyceride, made of glycerol molecules joined to three fatty acid chains by ester linkages.




Molecular structure of corn oil

The process of creating a biofuel is from corn oil is known as transesterification - transforming corn oil (an ester) into biofuel (another ester).

Method
> Add 100 m1 of corn oil into a 500 ml beaker
> In a separate beaker add 55.0 ml of methanol and 22.5 ml of 0.1 M NaOH solution.
> Place the beaker of corn oil on a hot plate, heat until 60 degrees Celsius
> Add the mixture from step 2 in eight phases, leaving 5 min between each phase. The temperature of the reaction mixture should be kept between 60 and 70 degrees Celsius to prevent it from spurting
> Let the mixture cool and separate over a week
> Place in a separating funnel and discard the lower layer (glycerol)
> Add 10 ml of 0.1 M acetic acid and invert the separating funnel gently 5 times
> Discard the lower layer
> Repeat the extraction step using 10 ml of distilled water
> Pour the the washed biofuel into a 100 ml beaker. Heat at 70-80 degrees Celsius for 10-15 min to evaporate the residual water.

Calculations for percentage yield
% yield = mass of dry biofuel/mass of corn oil x 100
= 69.84/89.26 x 100
= 78.2% (3sf)

NB: the final mass of the dry biofuel is lower than the actual value as spillage occurred during experimentation

Part 2: Determining the efficiency of fuels

In this demonstration, our teacher showed us how the efficiency of fuels can be determined by enthalpy changes.

Method
> Place 2 pieces of cotton wool at into a crucible
> Measure 10 ml of chosen fuel and pour into the crucible
> Measure 10 ml of distilled water into a clean 50 ml beaker
> Fix the beaker above the crucible using a retort stand
> Measure the initial temperature of the distilled water
> Ignite the fuel with a lighted splint and start the stopwatch
> Adjust the height of the beaker such that it is above the tip of the flame
> After 2 minutes, record the temperature of the water
> Extinguish the flame by covering it with a wire gauze with ceramic center

Results

Fuel
Initial temperature/˚C
Final temperature/˚C
Temperature change/˚C
Cyclohexane
31.0
75.0
+44.0
Methanol
31.0
100.0
+69.0


NB: Water reached boiling point in < 2 min when methanol was used as a fuel

Calculations for enthalpy change
We need to find the enthalpy (heat) change of water caused by one mole of fuel to determine its efficiency.

Enthalpy change of water = mass of water (kg) x specific heat capacity of water (kJ/ kg K) x change in temperature (˚C or K)
OR
q = mc∆T

NB: ˚C and K have same unit intervals and are interchangeable with reference to change in temperature
NB: specific heat capacity of water = 4.181 kJ/ kg K

Fuel
q (= mc∆T)
Cyclohexane
0.01 x 4.181 x 44 =1.83964 kJ
Methanol
0.01 x 4.181 x 69 =2.88489 kJ

Since we want to calculate the enthalpy change of water caused per mole of fuel, we need to calculate the amounts of fuel in moles.

Density of cyclohexane = 779.00 kg/m3
Mass of 10 ml of cyclohexane = 779 x 10/100x 1000 = 7.79 g
No. of moles of cyclohexane (C6H12) = 7.79/ (6 x 12.0 + 12 x 1.0) = 0.092738 mol

Density of methanol = 791.30 kg/m3
Mass of 10 ml of methanol = 791.3 x 10/1003 x 1000 = 7.931 g
No. of moles of methanol (CH3OH) = 7.931/ (12.0 + 4 x 1.0 + 16.0) = 0.24728 mol

Fuel
Enthalpy change per mol (kJ/mol) (3sf)
Cyclohexane
1.83964 ÷ 0.092378 = 19.9
Methanol
2.88489 ÷ 0.24728 = 11.7

Conclusion: Cyclohexane is the more efficient fuel

Sources of error
- Boiling point of water cannot exceed 100˚C and would affect the accuracy of measurement for methanol.
- Heat lost to surroundings
- Incomplete combustion of fuel due to insufficient oxygen
- Flame was extinguished after 2 min, hence not all the fuel was combusted

References
Image of triglyceride. Retrived from http://www.proteinpower.com/drmike/wp-content/uploads/2008/02/triglyceride.jpg
Image of corn oil molecule. Retrieved from https://sci9bestq3bm.wikispaces.com/Corn+Oil-Ensure

Saturday, October 5, 2013

Extraction of D-Limonene from orange peel

In this practical, we extracted D-Limonene, an essential oil from orange peel using steam distillation. D-Limonene not only smells great, it can be used as a fuel (it is combustible) and is green because it comes from a waste material, orange peel.

Properties of D-Limonene
- Density: 0.84 g/cm3
- Boiling point: 176 degrees Celsius
- Unsaturated hydrocarbon with chemical formula C10H16

D-Limonene

Method
> Scrape the white pith from the skins of 4 medium oranges
> Blend with distilled water until a fine puree is formed
> Transfer to 250 ml round-bottomed flask
> Attach flask to distillation apparatus. Turn on hotplate to highest setting
> When the thermometer shows 100 degrees Celsius, turn on the tap to run water through the condenser
> The distillate contains D-Limonene and water. D-Limonene should form a layer on top of the water and can be removed using a dropper
> If there is no distinct separation extract using NaCl and dichloromethane
> Confirm presence of D-Limonene by adding extract to aqueous bromine. Bromine should decolourise.




Distillation apparatus

D-Limonene forms a layer above water

Calculating yield

Mass of orange peel/g
50.50
Mass of d-limonene/g
1.20

% yield = mass of limonene/mass of orange peel x 100 
= 1.20/50.50 x 100 = 2.4%

D-Limonene yield is considerably higher than yield lavender essential oil, which is about 0.3% mass-for-mass.

Science behind
An essential oil is a concentrated hydrophobic liquid containing volatile aroma compounds from plantsThe essential oil of orange is made of more than 90% D-Limonene. D-Limonene is secreted from little pockets on the surface of orange peel and gives orange its distinctive smell.

Orange peel zest cells
SEM image of citrus peel

When the water and peel puree is heated, water and volatile compounds (including D-Limonene) vapourise and enter the condensor. They are then condensed to form the hydrosol, a mixture of water and orange essence. The D-Limonene, being hydrophobic and less dense than water, forms a layer on top of the water.

D-Limonene is used in perfumes and household cleaners for its fragrance. It is also a safe, effective and environmentally-friendly solvent used in adhesive and stain removers, cleaners and paint strippers.

Orange essential oil is a byproduct of orange juice manufacturing that can be obtained by centrifugation. D-Limonene can then be extracted from the orange oil by steam distillation. Because orange oil, unlike other essential oils, is a byproduct, it is one of the cheapest, making D-Limonene cost-effective.

References

Thursday, October 3, 2013

Paper Recycling

In this lesson, we made recycled paper.

Method
> Fill a fishtank with tap water
> Shred used paper into small pieces
> Blend with tap water until it forms a pulp mixture
> Pour the pulp into the fish tank filled with water
> Repeat until there is enough pulp in the fish tank to form a thin layer of paper pulp when passed through the screen
> Using the paper mould, remove some pulp from the fish tank, letting the water drain
> Place on a towel and let dry overnight
> Remove from the mould. This is recycled paper!







Paper is made of fibers (usually cellulose fibers derived from wood) pressed together.
Scanning electron microscope image of cross section of filter paper

When blended with water, the cellulose fibers are broken apart as water molecules disrupt the hydrogen bonds between them and they are re-suspended. Passing the pulp through the paper screen forms a thin layer of fibers on the screen. When dried, these fibers form hydrogen bonds to form a sheet of paper.

Industrial practice
Paper is mixed with water and chemicals to break it down, then heated and chopped to yield strands of cellulose. The resulting mixture is called a pulp or slurry. It is passed through screens which removes plastic or glue contaminants. The mixture is then cleaned, de-inked, bleached and mixed with water. It can then be made into new paper. The same fibers can be recycled about seven times, but the cellulose fibers get shorter each time, reducing the quality of the paper.

Benefits
Paper production accounts for about 35% of felled trees. Recycling paper saves trees. Recycling 1 ton of copier paper saves approximately 2 tons of wood. Recycling paper also uses less energy than making new paper.

We can also help by reducing our use of paper and re-using paper which reduces the need for recycling and paper manufacturing in the first place :)

References
http://en.wikipedia.org/wiki/Paper_recycling
http://en.wikipedia.org/wiki/Paper
http://www.sciencephoto.com/image/215422/350wm/H1000661-Filter_paper,_SEM-SPL.jpg