biodiesel from used kitchen grease or waste vegetable oil

8/14/2019 Biodiesel From Used Kitchen Grease or Waste Vegetable Oil

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Biodiesel From Used Kitchen Grease or Waste Vegetable Oil

This is how to make your own biodiesel fuel from used cooking oil. The oil -- waste vegetable oil(WVO), used fryer grease, animal fats, lard -- is often free for the taking. All you need is a fewcommon chemicals and some equipment you can easily buy or make yourself. The result is a cheap,clean-burning, non-toxic, renewable, high-quality diesel motor fuel you can use in your car without

modifications.

CAUTION: Wear proper protective gloves, apron, and eye protection and do not inhale any vapors.Methanol can cause blindness and death, and you don't even have to drink it, it's absorbed throughthe skin. Sodium hydroxide can cause severe burns and death. Together these two chemicals formsodium methoxide. This is an extremely caustic chemical. These are dangerous chemicals -- treatthem as such! Always have a hose running when working with them. The workspace must bethoroughly ventilated. No children or pets allowed. See Safety for further information.

Making biodiesel

Ingredients

Mixture:Waste vegetable oil (WVO) -- used cooking oil, fryer grease, animal fats, lardMethanol (CH3OH) -- 99%+ pureSodium hydroxide (NaOH -- caustic soda, lye) -- must be dry

Titration:Isopropyl alcohol (rubbing alcohol) -- 99%+ pureDistilled waterPhenolphthalein solution (not more than a year old, kept protected from strong light) -- "Phenol" or"Phenol Red" from swimming pool or hot tub supply stores may not be the same as

phenolphthalein; it can be used but the directions for use may be different

Washing:VinegarWater

Procedure

1. Filter WVO to remove any food scraps or solid particles.

2. Heat WVO to remove any watercontent (optional).

3. Perform titration to determine how much catalyst is needed.


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4. Prepare sodium methoxide.

5. Heat WVO, mix in the sodium methoxide while stirring.

6. Allow to settle, remove the glycerine.

7. Wash and dry.

8. Checkquality.

This procedure is called transesterification, similar to saponification. Sound familiar?Saponification is soap making. To make soap you take a transfatty acid or triglyceride (oil orkitchen grease) and blend it with a solution of sodium hydroxide (NaOH, caustic soda or lye) andwater. This reaction causes the ester chains to separate from the glycerine. These ester chains are

what becomes the soap. They're also called lipids. Their unique characteristic of being attracted topolar molecules such as water on one end and to non-polar molecules like oil on the other end iswhat makes them effective as soap.

In transesterification, lye and methanol are mixed to create sodium methoxide (Na+ CH3O-). Whenmixed in with the WVO this strong polar-bonded chemical breaks the transfatty acid into glycerineand also ester chains (biodiesel), along with some soap if you're not careful (more on that later). Theesters become methyl esters. They would be ethyl esters if reacted with booze (ethanol) instead ofmethanol.

Figures 1-3 show these two reactions. The zigzag lines in the triglyceride diagram (Figure 1) are

shorthand for carbon chains. At both ends of each line segment is a carbon atom.

Figure 1

In Figures 2 and 3 these zigzags are shorthanded as R1, 2 and 3.


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Figure 2

Figure 3

1. Filtering

Filter the WVO to remove food particles. You may have to warm it up a bit first to get it to runfreely, 95 deg F (35 deg C) should be enough. Use a double layer of cheesecloth in a funnel, or arestaurant or canteen-type coffee filter.

2. Removing the water

Many people heat the WVO first to remove any water content. Waste oil will probably containwater, which can slow down the reaction and cause saponification (soap formation). The less waterin the WVO the better.

This is how they do it. Raise the temperature to 212 deg F (100 deg C), hold it there and allow anywater to boil off. Use the mixer to avoid steam pockets forming below the oil and exploding,splashing hot oil out of the container. Or drain water puddles out from the bottom as they form --you can save any oil that comes out with the water later.

When boiling slows, raise the temperature to 265 deg F (130 deg C) for 10 minutes. Remove heatand allow to cool.

You may be lucky and find a regular source of WVO that doesn't need to have the water boiled off,in which case don't do it -- boiling means extra energy and time. Personally I don't boil off the waterfirst, I'd rather avoid the extra step in the process and save the energy it uses. But unless you're sure,

it may be better to be on the safe side.


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3. Titration

To determine the correct amount of lye required, a titration must be performed on the oil beingtransesterified. This is the most difficult step in the process, and the most critical -- make yourtitration as accurate as possible.

IMPORTANT: The lye must be dry -- keep it away from water, store it in an airtight container.

Make up a solution of one gram of lye to one liter of distilled water. Make sure it dissolvescompletely. This sample is then used as a reference tester for the titration process. It's important notto let the sample get contaminated, it can be used for many titrations.

Mix 10 milliliters of isopropyl alcohol in a small container with a 1 milliliter sample of WVO --make sure it's exactly 1 milliliter. Take the WVO titration sample from the reaction vessel (Figure 5#1) after it's been warmed up and stirred.

Add to this solution 2 drops of phenolphthalein, an acid-base indicator that's colorless in acid andred in base.

IMPORTANT: Phenolphthalein has a shelf life of about a year, it is very sensitive to degradationby light so after a while it will start giving erroneous readings.

Using a graduated eye dropper (with increments marked in tenths of milliliters) or some othercalibrated instrument (from medical supply outlets), while carefully keeping track of the amounts,drop measured amounts of the lye/water solution a couple of tenths of milliliters at a time into theWVO/isopropyl/phenolphthalein solution.

Follow each drop with vigorous stirring of the solution. In cold weather the WVO might congeal

and not work so you might need to do the titration in a heated room. If conditions are righteventually the solution turns pink (magenta), and stays pink for 10 seconds. This is the indicatorcolor for a pH range of 8-9 (see the photograph in the left column of this page, "Color of titratedliquid sample when at the correct pH"). It's important to find the exact amount, to just reach this pHwithout dropping in too much!

It's a good idea to do this entire process more than once to ensure that your number is correct. I'vefound that depending on the type of WVO, how hot it got in the fryer, what was cooked in it andhow long it was used, the amount of lye/water solution needed to titrate it is usually 1.5 to 3milliliters. You can also use litmus paper or a digital pH tester instead of the phenolphthalein. Try itwith fresh cooking oil from your kitchen too, it should need much less lye to reach pH 8-9.

The calculation

The next step is to determine the amount of lye needed for the reaction. Take the number ofmilliliters derived from the titration and multiply by the number of liters of WVO to betransesterified.

There is one more thing to be included in the calculation. Every liter of neat vegetable oil (fresh --never been cooked) needs 3.5 grams of lye for the reaction. So for every liter of WVO to be


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transesterified add an additional 3.5 grams of lye.

Example: The titration determined that it took 2.4 milliliters to reach pH 8-9 and you'll betransesterifying 150 liters of oil.

2.4 grams times 150 liters equals 360 grams lye

Plus 3.5 grams times 150 liters equals 525 grams lye

360 + 525 = 885 grams lye

If the titration result was 1.8 milliliters to reach pH 8-9, the final amount of lye needed for thereaction would be 795 grams.

I've found over time that the number of grams of lye needed per liter of WVO has generally beenbetween 6 and 7.

Test batches

The first few times you do this process or if you're planning on transesterifying a lot of WVO it is agood practice to first try out your lye amounts on a 1 liter batch in a kitchen blender. This worksreally well and you don't need to heat up the WVO too much, just enough so it will spin well in the

blender. Blenders are very thorough at mixing the ingredients so heating is not as critical.

Start by mixing up the lye and methanol in a blender (one that will never be used for food again).First make sure the blender and all utensils used are dry. Forming the exothermal sodium methoxide

polar molecule will heat up the blender container a bit. Keep mixing until all the lye has beendissolved.

Once the sodium methoxide is prepared, add to the blender 1 liter of WVO. Make certain all yourweights and volumes are precise. If you're unsure of the titration result numbers then use 6-6.25grams of lye per liter of used WVO, or 3.5 grams for fresh vegetable oil. Blender batches need only

be run for about 15-20 minutes for separation to be completed before switching off. The settlingtakes some time to complete. The solution can be poured from the blender into another containerright after switching off the blender.

It is good to do a few batches with varying amounts of lye recorded so later when checking resultsone can choose the lye quantity that did the best job.

When too much lye is used the result can be a troublesome gel that is tough to do anything with.(See Glop soap.) When not enough lye is used the reaction does not go far enough so someunreacted WVO will be mixed with the biodiesel and glycerine. This will form three levels with

biodiesel on top above unreacted WVO with glycerine on the bottom. If there is too much water inthe WVO it will form soaps and settle right above the glycerine forming a fourth level in thecontainer. This layer is not too easy to separate from the unreacted WVO and glycerine layers.

4. Preparing the sodium methoxide

Generally the amount of methanol needed is 20% of the WVO by mass. The densities of these twoliquids are fairly close so measuring 20% of methanol by volume should be about right. To be


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completely sure, measure out a half-liter of both fluids, weigh, and calculate exactly what 20% bymass is. Different WVOs can have different densities depending on what type of oil it originallywas and how long it was used in the deep fryer.

Example: When transesterifying 100 liters of WVO, use 20 liters of methanol.

The methanol is mixed into a solution with the sodium hydroxide (lye), creating sodium methoxidein an exothermic reaction (ie it gets warm from bonds forming). Keep all utensils the lye comes in

contact with as dry as possible.

CAUTION:Treat sodium methoxide with extreme caution! Do not inhale any vapors! If any sodium methoxidegets splashed on your skin, it will burn you without your feeling it (killing the nerves) -- washimmediately with lots of water. Always have a hose running when working with sodium methoxide.

Sodium methoxide is also very corrosive to paints. Lye reacts with aluminum, tin and zinc. Useglass, enamel or stainless steel containers -- stainless steel is best. Used restaurant equipment supplystores and scrap metal recycling yards are two good places to look for this type of equipment. Brazeon plumbing fittings for drains, etc. where needed.

5. Heating and mixing

Pre-heat WVO reclaimed from a restaurant's waste grease barrel to 120-130 deg F (48-54 deg C).

A propeller or paint stirrer coupled to a 1/2-inch electric drill works fine as a mixer.

Too much agitation causes splashing and bubbles through vortexing and reduces mix efficiency.

There should be a vortex just appearing on the surface. Adjust the speed, or the pitch or size of thestirrer to get the right effect.

If you want a quieter processor, an electric pump plumbed to form a mixing loop for stirring theWVO would do a nice job. Mount the pump above the level that glycerine will gel at to preventclogging up the pump (see below).

Add the sodium methoxide to the WVO while stirring; stir the mixture for 50 minutes to an hour.The reaction is often complete in 30 minutes, but longer is better.

The transesterification process separates the methyl esters from the glycerine. The CH3O of the

methanol then caps off the ester chains and OH from the NaOH (lye) stabilizes the glycerine.

6. Settling and separation

Allow the solution to sit and cool for at least eight hours, preferably longer. The methyl esters --biodiesel -- will be floating on top while the denser glycerine will have congealed on the bottom ofthe container forming a hard gelatinous mass (the mixing pump must be mounted above this level).

An alternative method is to allow the reactants to sit for at least an hour after mixing while keepingthe brew above 100 deg F (38 deg C), which keeps the glycerine semi-liquid (it solidifies below 100deg F). Then carefully decant the biodiesel.


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This can be done by draining the reactants out of the bottom of the container through a transparenthose. The semi-liquid glycerine has a dark brown color; the biodiesel is honey-colored. Keep awatch on what flows through the sight tube: when the lighter-colored biodiesel appears divert it to aseparate container. If any biodiesel stays with the glycerine it is easy to retrieve it later once theglycerine has solidified.

If you left the mixture in the tank until the glycerine gelled, reheat the tank just enough to liquify theglycerine again. Don't stir it! Then decant it out as above.

Figure 4 shows one example of a system for separating two liquids with different densities. Thiscould make a good pre-filter or be used to separate oils, soap and glycerine/esters goop. Marine/boatfuel cleaning systems do a good job of filtering.

Figure 4 Figure 5

Figure 5 shows the reaction vessel (#1) where the WVO is mixed (also could be done with a pump)and heated. Heating is accomplished by (#2) a hotplate, propane-burner, or a diesel stove would

work well.

A proposed alternative using very little electricity is illustrated in Figure 6.This system would use a furnace-type burner run on reclaimed esters toheat its reaction vessel. The vessel's stirring action is created by thermoinversion currents generated by the vessel's external cooling tubes and a

baffled exhaust vent that runs up through its center.

Figure 5 also shows a blender (#3) used to mix up the sodium methoxide.When making 16 liter (5 gal) batches, I use a yard-sale glass blender for thesodium methoxide solution (and for nothing else!), but I can't fit it all in at

once, so I measure out three separate portions.Glycerine

The glycerine from WVO is brown and usually turns to a solid below about 100 deg F (38 deg C).Glycerine from fresh oil often stays a liquid at lower temperatures.

Reclaimed glycerine can be composted after being vented for three weeks to allow residualmethanol to evaporate off or after heating it to 150 deg F (66 deg C) to boil off any methanolcontent (the boiling point of methanol is 148.5 deg F, 64.7 deg C). The excess methanol can berecovered for re-use when boiled off if you run the vapors through a condenser.

Another way of disposing of the glycerine, though a great bit more complicated, would be toseparate its components, mostly methanol, pure glycerine and wax. This is often accomplished bydistilling it, but glycerine has a high boiling point even under high vacuum so this method is

Figure 6


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difficult.

The glycerine by-product makes an excellent industrial-type degreaser/soap. One way to purify it isheat it to 150 deg F (65.5 deg C) to boil off excess methanol, making it safe for skin contact (take

precautions with fumes). Once the glycerine is back to a liquid the impurities sink to the bottom andthe color will become a more uniform dark brown. This can be cut with water leaving it a tan color,less concentrated and softer and easier to handle when washing hands. Produced this way thedegreaser could be sold in squeeze or pump dispensers.

Other ideas for disposing of the glycerine are breaking it down to usable methane gas, with amethane digester or, for a much wilder idea, it could be broken down with pyrolisis. Pyrolisis wasused extensively to run cars on firewood in oil-scarce Europe and elsewhere during World War 2.The processor has a heat source that heats the fuel (wood or glycerine) in an airtight box withoutoxygen. This allows the fuel to release its methane while not allowing it to burn. The methane istrapped in an inflatable storage container or compressed into a tank. This is an area of biodieseldevelopment that warrants further work.

Soap residue

Suspended in the biodiesel will also be some soapy residues. These are the result of Na+ ions fromthe sodium hydroxide (NaOH) reacting with water created when the methanol bonds with the esterchains along with any other water that was suspended in the WVO.

If the reaction produces more than the usual amount of soap, this happens when lye comes intocontact with water before it has a chance to react with the WVO -- in this case the excess watershould have been boiled off first. (See Step 2, above, Removing the water.)

The part of the process where it's vital to keep all water out of the reaction is when making the

sodium methoxide. Keep the blender and all utensils the lye comes in contact with as dry aspossible. The chances of a good clean splitting of esters from glycerine with little soap by-productare much better on a warm dry summer day than on a damp winter day.

7. Washing and drying

There is more than one school of thought on getting the biodiesel from this stage to the fuel tank.One is to let it sit for a while (about a week), allowing the majority of the soap residues to settle

before running the biodiesel through a filtration system then into the vehicle/home fuel tank.

Another method is to wash the soaps out of the fuel with water, one or more times. When washingbiodiesel the first time it's best to add a small amount of acetic acid (vinegar) before adding thewater. The acetic acid brings the pH of the solution closer to neutral because it neutralizes and dropsout any lye suspended in the biodiesel.

Figure 7 shows a simple way of washing using a translucent PVC type container with a valve 3-4inches from bottom. For 5 gallon batches use those 5-7 gallon buckets found everywhere these days.If a translucent container can't be found one fabricated with a sight tube (#6) ought to work.

Fill with water until it is halfway between the container's bottom and the valve, then fill up with thebiodiesel to be washed. After a gentle stirring (keep it gentle, you don't want to agitate up soaps)


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followed by 12-24 hours of settling, the oil and water will separate, the cleaned oilcan be decanted out the valve, leaving the denser soapy water to be drained out the

bottom (#5).

This process might have to be repeated two or three times to remove close to 100%of soaps. The second and third washings can be done with water alone. After thethird washing any remaining water gets removed by re-heating the oil slowly(Figure 8), the water and other impurities sink to bottom. The finished product

should be pH 7, checked with litmus paper or with a digital pH tester.

The water from the third wash can be used for the first or second washes for the next batch. Theimpurities can be left in the re-heater for the next batch and removed when it accumulates. Thesoaps can be concentrated, left-over biodiesel can be decanted out and what's left isa biodegradable soap good for many industrial-type uses (degreasers etc.).

I had some success with trapping the concentrated very hydrated sodium from thissoap. The way I did this was by pouring the soap onto a stretched cheese cloth and

allowing the water to run through leaving the sodium on the cloth. This is as far asI've gone with this so far but it seems one could press much of the water from thesodium then vacuum dessicate this saturated sodium under dry conditions back to ausable sodium hydroxide.

Transesterified and washed biodiesel will become clearer over time as anyremaining soaps drop out of the solution.

Another idea I have been working with is chilling down the biodiesel thus allowing the soaps tocondense and settle out faster. When the oil gets chilled it seems to speed up the settling of theresidual lye. With a short settling time the oil clears considerably.

Bubble washing

Some experimenters are getting good results with the Idaho bubble washing technique. It takeslonger, but uses less water. They find it very effective, giving a clean, polished product.

Here's how they do it. The bubbles are formed by compressed air passing through an air stone. For asmall installation, buy an aerator at an aquarium shop -- they come in several sizes and cost about$10 to $40. Sometimes they have a filter attached -- throw it away.

Add about 30 milliliters of vinegar (acetic acid) per 100 liters of biodiesel and then about 50%water. Then drop in the air stone.

The air stone sinks to the bottom of the tank. When you switch on the aerator, the air bubbles risethrough the biodiesel, carrying a film of water which washes the biodiesel as it passes through. Atthe surface, the bubble bursts, leaving a small drop of water which sinks back down through the

biodiesel, washing again.

If the mixture is still cloudy after a couple of hours, add a little more vinegar.

Bubble-wash for 12 hours or longer (up to 24), then drain off the washing water, skim off any waxfloating on top. Repeat the bubble wash two more times; keep the water from the 2nd and 3rd wash

Figure 7

Figure 8


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for washing the next batch.

For severe soap formations, first heat the biodiesel/soap mixture to 122 deg F (50 deg C). Addenough vinegar to bring the pH to slightly below 7. Stir for half an hour, cool and continue with

bubble drying as usual.

See also Bubble washing

8. Quality

The quality of the fuel product can be checked by visually examining it and checking its pH. The pHof the finished product can be checked with pH paper or a digital tester. It should be neutral (pH 7).It should look like clear vegetable oil with a light brown tint, similar to filtered apple cider.

There are not supposed to be any films, particles or cloudiness to it. Films would be remainingsoapy residue, re-wash or re-filter it at 5 micron or finer. Cloudiness would be water still in it, re-heat it. Particles could be anything and indicates the filter is failing.

Any oils will clear up considerably when heated but the test is, when it cools back down is it stillclear? If it is not yet clear then allowing it to settle out for an additional week or two should beenough to clear it up.

For final filtering it is best to use a marine-type fuel filter -- the ones with a transparent canister so itis possible to keep an eye on the fuel's clarity. I used to trust when I washed it to just pouring fuelinto the tank through folded cheesecloth in a funnel. After running into an increased number of dirtyfuel filters I've become more careful.

It is important to know also that biodiesel does a great job of cleaning up fossil diesel fuel filmscoating the interior parts of any old diesel engine. For this reason, take care to check and changeyour vehicle's fuel filters when first switching over to biodiesel. I like putting a small, cheap, clearor translucent plastic in-line fuel filter right before my vehicle's stock filter. This will prefilter thefuel before it reaches the vehicle's fuel filter, which is more expensive to replace. This also makes iteasy to see when fuel is flowing and to keep an eye on the condition of the filter.

Limitations

Biodiesel does have some limitations. First it has cold-weather starting problems. Depending on thetype of oil used, around 40 deg F (4-5 deg C) it may start to solidify. One remedy is to mix with a

proportion of fossil diesel. Or try a Racor or Diesel-Therm electric fuel heater. Heated garages arenice too. Some people report that standard antigelling compounds work fine, others say they'reunpredictable. (Be aware that antigelling agents can be highly toxic.)

Retard the injection timing by 2-3 degrees -- this overcomes some of the effect of biodiesel's highercetane number. The engine loses a bit of the extra power you get with biodiesel, but it runs quieterand the fuel burns cooler, reducing NOx emissions. (See also NOx emissions and biodiesel.)

There can be an increased rate of corrosion of rubber parts in the fuel system over time with 100%

biodiesel. Newer cars do not use rubber parts. Biodiesel has been used in many older motorswithout any problems. Viton parts are best, but others are just as good.

biodiesel from used kitchen grease or waste vegetable oil

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