In response to numerous questions about what happens to the collected algae this instructable should help someone to build a microbial fuel cell (MFC) with household items and materials. As its name suggests, an MFC uses microbes to catalyze electricity-producing reactions.

This instructable is based on work done by Bruce Logan and his team at Penn State University and on the microbial fuel cells built by Abbie Groff, a student at Conestoga Valley High School in Lancaster, PA. The research she performed with her MFCs helped her win the Grand Champion Award at the 2005 Lancaster County Science Fair.

Now to be completely honest the fuel cell we will build is not "purely" an algae fuel cell, it is a microbial fuel cell that uses anaerobic bacteria to decompose organic matter, in our case dead algae.

The fuel cell will consume the algae (or other organic material) with two significant by-products, electricity (always useful) and methane gas. In a production system the methane must be captured for further use for instance as fuel for a steam powered generator which processes its exhaust plume through an algae based (or other) exhaust gas scrubber.

In this design its very cleverly captured in the sealed anode and if you come up with some clever way to do something with it, I'd be very pleased to hear it.

Step 1: Bill of Materials


Drill or drill press
Razor knife or scissors
Hot glue gun
Funnel - Optional for filling bottles
Soldering iron
Lead Solder
Materials and where I got them. I have no relationship with any of these stores or products. They are inexpensive and should be commonly available:

  • Two heavy duty plastic bottles with sealable lids. Wide mouth bottles are best choice for ease of inserting broad surface area electrodes.
  • Low power aquarium air pump
I recommend the Hagen Elite 799 available at PetSmart for around $6. Rated at 1.8W.
  • 1 x 2" PVC pipe 1-2 feet long
  • 2 x 1 quart mason jars or similar
  • 1 x 2" PVC Nipple or Sprinkler system riser
  • 4 x PVC slip caps. You can probably get away with two, I use two for storing the salt bridge
  • 2 x 1in square Silkscreen material or other nonconductive mesh
Cut to 2 circles that match the outdiameter of the PVC nipple
  • Agar - 100g per Liter of water
  • Salt - 400g per Liter of water ( 14 oz/Qt ).
  • Carbon cloth or carbon paper
Carbon cloth of various types can be purchased online. These folks http://www.uscomposites.com/carbonpage.html offer it for around $40/yd. I'm using plain old fashioned carbon paper with wire mesh support. Eventually I plan to experiment with alternative designs that use carbon filtration technologies.

  • Nitrogen for removing oxygen from water. This can be readily obtained from several sources locally and online.
    • Welding supply places will have Nitrogen and Argon in tanks for various sizes. Around $35 for a small tank here.
    • Local tire dealers. Local tire dealers often replace air in tires with nitrogen (for a fee). They will happily fill up your inner tube or inexpensive pressure tank (for a fee).
    • Bacteria for a MFC can be obtained from several sources.
    • Shultz Liquid Plant food
Most likely, wastewater or anaerobic sediments will initially contain enough organic matter to serve as food for the bacteria, but this will eventually run out. Algae will provide the food source (substrate) used to maintain the MFC. The liquid plant food and soil water will provide trace minerals and nutriets.

Step 2: Preparing the Electrolyte

Okay so here's the first tricky bit. We're going to make an algar/salt solution and use it to fill the salt bridge. Now the really clever bit is figuring out how to keep the salt bridge upright while the agar cools.

Agar can be obtained from health food stores and high end supermarkets with health food departments. The clerks will be able to help you if you ask if they carry 'the dietary supplement agar and calcium supplements with calcium carbonate because a friend recommended them" instead "Hey, you guys got any stuff for a microbial reactor salt bridge?"

Preparing Tablet or Powdered Agar:

Dissolve 1 bar, 10 tablets or 7 grams of powdered agar in 1/2 quart of the soilwater we prepared in the last step. Warm the agar in a hot water bath by placing it in a glass bottle. Heat water on the stove until just about boiling, remove from heat and place the agar bottle in the water. The microwave is another good way. Simply heat up a bowl of water and place the bottle with agar in the center.

As it warms the agar will begin to melt, warm the agar until it becomes liquid. Add the salt and mix well to dissolve the salt in the agar. Remove from the heat

Dissolving salt:

  • Finely ground salt such as canners salt or table salt dissolves much faster than coarsely ground salt (rock salt).
  • It is not clear that all salt added must be dissolved if a solution is to obtain maximum electron exchange
  • Salt dissolves much faster in hot water than in cold water.
  • Salt dissolves much slower as the salt concentration increases. The last bit of salt may take a long ime to dissolve.
  • Agitation greatly increases the rate at which salt dissolves
  • A layer of salt on the bottom may take days to dissolve if left undisturbed

Step 3: Making the Salt Bridge

Now that we've prepared the agar/salt electrolyte solution we're going to fill the salt bridge with it. Here's what I recommend.

Get a short glass large enough to hold the bridge PVC upright. Cut a piece of cardboard large enough to span the glass and at least double the size of the bridge pipe. Cut a circular hole in the center that matches the outer diameter of the bridge.

Place a PVC nipple on one end of the pipe. Insert the pipe though the hole in the cardboard and place in the glass so that it is standing on the flat end of the nipple. This should hold the bridge upright while the agar cools and solidifies.

Now carefully take the melted agar/saline solution and using the funnel fill the salt bridge to the top. I found that wrapping a wash cloth around the base of the pipe where it exits the cardboard made overflow much easier to deal with when filling the bridge. Carefully place a second PVC cap on the end to prevent accidental spillage and allow to cool.

Once the agar has cooled and solidified remove it from the assembly. It may be stored in the refrigerator.

Now using a drill or drill press with a large diameter bit drill out the end of two PVC slip caps leaving a short collar around the end. When the slip is placed over the end of the salt bridge it should hold a circular piece of non-conductive/non-reactive mesh such as plastic silk screen material firmly in place.

Step 4: Obtaining Culture Media

As I mentioned in the introduction this is not truly an algae based fuel cell. This fuel cell relies upon algae to provide biomass feedstock for the production of electricity, methane and CO2. The fuel cell itself is driven by bacteria adapted to live in sediment where no oxygen is found. These anaerobic bacteria can be obtained from several sources.

One of the recommendations from the folks at Penn State was to obtain some primary affuent (waste water) from the local water purification plant. But that was just too icky.

Anaerobic bacteria are also found in the benthic zone. According to Wikipedia:

The benthic zone is the ecological region at the lowest level of a body of water such as an ocean or a lake, including the sediment surface and some sub-surface layers. Organisms living in this zone are called benthos. They generally live in close relationship with the substrate bottom; many such organisms are permanently attached to the bottom. The superficial layer of the soil lining the given body of water is an integral part of the benthic zone, as it influences greatly the biological activity which takes place there. Examples of contact soil layers include sand bottoms, rock outcrops, coral, and bay mud.

Therefore much like we obtained our algae culture from natural sources we will obtain culture amples from available natural resources.

So go to a local lake or creek, a swamp is good if you're lucky enough to have one. If you fish or you are have a friend who fishes ask them where the best catfish or suckers are to be found. Tell them you're looking for bottom feeders which indicates a rich organic base.

Basically you're going to wade into the water until you're pretty deep in bottom muck, optimally the water will cover the tube when it is buried to obtain the sample. Push or drive the tube into the bottom to a depth of at least 6" inches or more. If the tube is not fully submerged when the sample is taken fill it before inserting and "top it off" with lake, pond or running water take water from near the bottom if possible.

Tilt the pipe over and place a slip cap over the mud end. Top off the pipe with ambient water and place a slip cap over the other end. Keep the pipe closed until you are ready to use it ( step 7 I think ). The bacteria of interest are anaerobic which means we want to expose it to oxygen as LITTLE as possible.

Once again wikipedia provides:

Anaerobic is a technical word which literally means without air (where "air" is generally used to mean oxygen), as opposed to aerobic.

In wastewater treatment the absence of oxygen is indicated as anoxic; and anaerobic is used to indicate the absence of a common electron acceptor such as nitrate, sulfate or oxygen. An anaerobic adhesive is a bonding agent that does not cure in the presence of air.

Take each of the mason jars and scoop down deep in the bed, possibly scooping down several times. Fill each jar with deep mud. This should generally insure that you get a good healthy sample of bacteria along with sufficient additional material to create high quaility nutrient media.

Try to disturb the water and bed as little as possible fill the Mason jars with ambient water. This will capture trace elements which may be present and beneficial to our bacteria.

Leave everything alone until we're ready to use them.

So now we're going to make a salt bridge.

Step 5: Constructing the Electrodes

Layers of copper/galvanized steel mesh
carbon paper

Copper Mesh Swatches from TWP Inc.

Almost any conductive metal mesh such as window screen mesh. I'm particularly excited about investigating the role of galvanized steel and zinc mesh. The most efficient MFC electrodes use a very expensive platinum or titanium catalyst. However zinc is so closely associated with effective energy transfer that it be very interesting indeed.

In this case both electrodes will be constructed using the same technology, layers of carbon paper interlaced with layers of wire mesh. The carbon paper layers are slightly smaller in size than the mesh layers. Copper wire is soldered to the exposed wire mesh around the edge.

Wire mesh layers should be placed on the outside to contain the carbon paper and maintain integrity of the electrodes in the mud or sand. The assembly should be tight to ensure good connectivity between the carbon and mesh layers plus circulation of media and water.

Apply solder liberally around the outside edge to ensure the best connectivity between the layers.

Once the electrodes have been assembled the exposed metal mesh should be protected with a good coating of hot glue.

Now we will insert the electrodes into the caps for later assembly into the MFC.

Drill a small hole in the center of one of the caps and a larger 1/4" hole off to the side. Pass the electrode wire through the small hole leaving the electrode to dangle where it will be approximately centered in the jar. Seal the wire hole with hot glue.

Push a length of air through the hole long enough to reach to the bottom of the cathode jar. Insert the air stone into the tube and seal. Seal the hole around the tube with hot glue or epoxy.

This assembly is called the cathode top and electrode.

Take the lid for the other jar. Pass the wire from the second electrode through that, also placed so that it hang approximately in the middle of the jar. The bacteria culture fed by the vinegar should thrive in the de-gassed water and it should not be necessary to bury the electrode in the mud.

Now that the sub-assemblies are complete we are ready to put our MFC together and fire it up.

Step 6: Assembling the Reactor - Part I

Now its time to bring it all home.

Cut a hole in each of the reactor bottles at the same height equal to the outside diameter of the slip caps. Holding the bridge pipe upright remove the temporary slip cap. Cut a circle of silkscreen material (pantyhose might work) or other plastic mesh to the diameter of the pipe. Place the silkscreen over the agar. Now get the slip caps we drilled out when we created the salt bridge and verify that they hold the agar/electrolyte. Place glue on the pipe and seat the slip cap.

Depending on the screen material used to hold the agar/electrolyte solution in place it it probably possible to use the slip bushing (pictured). This would be secured to the side of the bottle and the saltr bridge inserted into with a sleeve of retaining mesh held in place by the bushing. The bushing is held in place with hot glue and the salt bridge secured with it.

Now we're going to prepare a conductive solution for the cathode chamber. Again using the solubility of salt maxes out at 400g/L we're going to prepare enough solution fill one bottle. Heating the water and other suggestions that were used during creating the salt bridge also apply here. If heat is used allow the water to cool completely before proceeding.

Step 7: Assembling the Reactor - Part II Assembling the Cathode

In this design the two chambers are not particularly distinct. At the moment I am inclined to think that they should be approximately equal but that may be nothing other than my own compulsion to symmetry.

Pick one chamber for the cathode (saltwater/electrolyte chamber) and one chamber for the anode (mud/culture chamber).

Prepare enough salt solution to fill the cathode chamber following the procedure outlined in step 3 without the agar. When the solution has cooled fill the cathode chamber with the electrolyte.

Now place the cathode cap containing the air hose, bubbler stone and electrode on the cathode. Approximately center the electrode in the jar and close the lid fully then open a small amount to allow air to vent.

Next we will populate the anode chamber with bacteria and culture media which should produce electricity.

Step 8: Assembling the Reactor - Part III Assembling the Anode

Now we turn our attention back to the we obtained earlier. The collected water will be used as culture media and the mud in the pipe will be used to provide the culture.

We'll be diverging from Abbie's design a bit. Where Abbie used the actual mud we're going to try to extract a sample and culture the bacterium.

I have been advised by Dr. Logan at Penn State that they do not de-gas the influent since the bacteria will handle it due to the low solubility of oxygen. The material in italics may be bypassed but I left it in case anyone ever wants to de-gasify water for some reason.

"'To do that we're going to de-gas the water using nitrogen, argon or other inert gas. Strictly speaking you don't have to do this but it will give our bacteria a better chance to breed.

We're going to do it slowly. Since the options for obtaining gas range from inner tube to pressure tank I give you the following simple instruction. Connect a section of aquarium air tube to the end of a hose that is connected to the gas reserve. Hopefully you have some way to regulate the gas. If you're using an inner tube I suggest filling a balloon (insert it over the valve and push the valve in) and using that to dispense the gas by inserting the air hose into the end and letting the gas slowly out of the balloon. Yeah, I know, it ain't easy being that cheap. Get over it or spend some money for a tank with a valve.

Now having arranged by some mechanism to regulate the gas flow of the nitrogen into the air tube attach the bubbler stone to it. Fill the anode chamber (one bottle) with the culture media water. Agitate well. Insert the bubbler stone into it and slowly bubble nitrogen through the solution.

How much nitrogen to bubble and for how long? A very, very good question and as soon as I have an answer I'll update this. I've asked the folks at Penn State so its not impossible this will be updated. Try to stretch it out, say 15 minutes maybe stirring occassionally.

If you've got the nitrogen do both bottles since we'll be topping off the culture media.

Once you've de-gassified the water or not its time to introduce the culture (mud).

This is also the time to put in some algae sludge if you have some.

See I said it was an algae fuel cell....

Grab the sample pipe and place the mud end in the anode chamber preferably under water before removing the slip cap. You might need to push it off with a long screwdriver or kitchen fork. Pull the slip cap off of the other end and slowly begin pushing mud out with a dowel or broom handle. You want to push out the bottom 2-3 inches of mud then take out the pipe. This should give you a solid culture of primarily anaerobic bacteria. Top off the culture media if needed from the second jar and add 2 drops of vinegar for each quart of culture media in the jar to supplement the natural nutrients.

Now place the anode cap and electrode in the anode jar and seal the edge with hot glue. The anode should be air tight and is not designed to be recharged at this time. Once the food is exhausted the bacteria will die. This will be indicated by a drop off in the output voltages.

Because the MFC cannot be recharged it is properly called a battery. To rectify this (get, a little electrical joke...very little) use a container which gives a solid, air tight seal and add a feeder hole and tube to it. Remember to seal the feeder tube when not in use and preferably flush with nitrogen.

Step 9: Operating Your MFC

Now if you attach an external circuit through a resistor you should begin getting voltage out of your MFC. The voltage will increase the bacterial population grows and then begin to decrease.

If you don't get voltage there could be any number of good reasons, including the culture. Try again, make sure you get a good seal on the anode.

Electrode construction and connectivity is also important.

For more information and design alternative on Microbial fuel cells I recommend

Dr. Bruce Logan's excellent work

Abigail Groff's outstanding page on her award winning project. Without her work this instructable would not be done.

And don't forget the folks at MicrobialFuelCell.org

I hope you enjoyed this instructable, I will be updating and revising as time goes on.
<p>how many volts produced?</p>
<p>Hi, I am going to make a mfc. I used 10 lit containers for anode and cathode chambers and 3 inch dia. pvc pipe for salt bridge. Now i am unable to get graphite electrodes. Kindly guide me, what should I do? Can I use carbon brushes for this purpose?</p><p>If yes then what shuold be its size. ? Kindly help me as soon as possible. </p>
<p>Carbon brushes used in washing machines and large dc motors should be good enough for 10 litres setup . Also i would recommend using 3 containers of about 3-4 litre capacity and they can be connected externally in parallel </p>
<p>HI, I am wiki. I am going to make a mfc with 10 lit chambers i.e anode and cathode with 3 inch dia. pvc pipe as a salt bridge. Now i am unable to find graphite electrodes.</p><p>kindly guide me as soon as possibe.</p><p>Can i use carbon burshes as electrodes? if yes then what should be its size?</p>
<p>Great instructions. I'm planning to give it a go.</p><p>I'm trying to understand the step: &quot;Once the electrodes have been assembled the exposed metal mesh should be protected with a good coating of hot glue.&quot;</p><p>A picture would have been helpful.</p><p>Do you completely cover both sides of the mesh (as in trying to completely seal it to make sure not water gets in), or do you only do one side of the electrode, or do you leave an opening in it for the solution to make contact? </p><p>Please explain a wee bit more. </p>
<p>This was a very early prototype and you might find some of the other designs more efficient. I switch to using various types of carbon electrodes.</p><p>The hot glue is to seal the electrode around the edges and cover any projecting metal bits that stick out past the solder. The main body must be exposed to the medium.</p>
<p>Can this wire be used as electrodes in the above MFC?</p><p><a href="http://www.amazon.com/Plastic-Coated-Value-Coils-24-Translucent/dp/B003K7AINE/ref=pd_sim_ac_2?ie=UTF8&refRID=0HFMH4R2WEZ14MCPN2D8" rel="nofollow">http://www.amazon.com/Plastic-Coated-Value-Coils-2...</a></p><p>Thanks.</p>
That link doesn't seem to be working any more. From the text of the link I would expect the plastic coating to insulate the wires and prevent the MFC from working properly.<br><br>The electrode(s) must be conductive, however they do not need to be carbon. Carbon is used by the scientific community to prevent any secondary reactions from interfering with the measurements but that is not a production requirement.
<p>Can you explain how electrons are generated from the bacteria and then transferred from the bacteria to the electrode?</p><p>Thanks!</p>
<p>The last time I checked the research the process was not well understood. From what I understand certain types of anaerobic bacteria generate electricity as a side effect of biological processes. The research has, as far as I know, focused primarily on identifying the strains that demonstrate this the most.</p>
<p>How long will this experiment take approximately?</p>
<p>Initial energy production should begin within a few days and will run as long as there are nutrients to feed the organisms. The salt bridge is subject to breakdown over time and the electrolyte could eventually be depleted and need replacement.</p>
<p>I'm a student who tried to build an mfc at home. I used waste water as the anode substance, and carbon electrodes, in both anode and cathode. but im not getting any voltage reading. is their something wrong?</p>
<p>There's not enough information for me to make any sort of an informed guess. What sort of waste water did you use and what did you use to create the individual cells? There are more detailed instructions in Part II.</p>
Does electric current is obtained spontaneously or take some hours for the process? <br>
It takes a while for current to ramp up. Its a function of volume and colony size.
Hi. i want to do a project on the MFCs, the problem im facing now is with the length of agar-salt bridge. so I want to know the length of the agar-salt bridge for a working volume of 1 lit or 2 lit inoculum and it retention time also. how long did a agar-salt bridge is capable of holding a MFC??
What kind of waste does the MCF produce?
It seems to me that a resistor is necessary to a fuel cell's operation. What resistance, in this manner, should be applied?
As you probably know resistance is a function of load. This design, as with many others, are designed for scientific purposes ( such as science fair projects ). Due to natural variation in resistor manufacturing ( normally +- 10% ) the only scientifically reproduceable voltage is the open circuit voltage. Obviously once a load is applied current and voltage vary.<br><br>Generally speaking this sort of design is best suited to trickle charge applications.
Ok thanks.
hello egbertfitzwilly......<br> I m making a microbial fuel cell in which i am using a sulfides as a substrate.. and aerobic bacterial cultures. i made a two nylone made chambers with salt bridge. Now i am about to start my work and my guide told me to staderdize a fuel cell,,, so i am not getting how to standerdize a fuel cell with a use of sulfides as a subsrate. i need a help with every type of actions which carry out a good work. it will be a great help of you if you guide me as any......<br>
Try this design:<br><br>https://www.instructables.com/id/Make-a-Microbial-Fuel-Cell-MFC-Part-II/
Do you have to use agar.
No, if you you look at my other instructables I've substituted Knox unflavored gelatin.
Hi,<br> I'm a student who tried to build an mfc at home. I used waste water as the anode substance, and graphite electrodes, in both anode and cathode. But my multimeter is showing a negative voltage reading. What have I done wrong?<br>
If you are showing a negative non-zero voltage you have connected your voltmeter backwards.
A couple of thoughts on de-gassing:<br><br>One quick way to degas a solution is to boil it for a few minutes. Gas solubility decreases a lot with temperature. Of course you won't be able to boil your culture, but sterilizing the media might help to keep stray yeasts out of it.<br>Other gases will work as well, such as helium, which is more readily available for party ballons in smaller disposable cylinders. <br><br>You can also remove the oxygen specifically by electrolyzing the solution since you have nice electrodes and a very fine salt bridge. During the electrolysis of salt water, at the cathode (-) side dissolved oxygen is reduced to hydroxide, OH-, and hydrogen gas is evolved. In the other compartment, the anode(+), oxygen gas is evolved, while acidifying the adjacent solution.
Thank you for this excellent input. I will experiment with this for my other &quot;How to make Sodium Hydroxide&quot; instructable series...
This is really cool. Just wondering how many amps are you able to pull out of it and in that condition what was the output voltage. In other words what's the maximun output power you're able to achieve? <br><br>Does the algae have to have sunlight in order to do its thing?<br><br>Keep rocking this kind of cool stuff.
Thank you for these kind words.<br><br>There is no relationship between microbial fuel cells and algae scrubbers. The output voltage from an MFC varies according to volume, microbe type and available food.
side topic: New application for MFCs - desalination. This might interest you:<br/><br/>&#8220;Water desalination can be accomplished without electrical energy input or high water pressure by using a source of organic matter as the fuel to desalinate water,&#8221; reported in a recent online issue of Environmental Science and Technology. Please read more at <br/><br/><a rel="nofollow" href="http://earthalternate.blogspot.com/2009/08/electricity-and-desalination-from.html">http://earthalternate.blogspot.com/2009/08/electricity-and-desalination-from.html</a><br/>
tell me more<br>i was looking for this kind of solution for months<br>wow is this a miracle or what ?
I'd say its more in the &quot;or what&quot; category.....
the blog isnt showing up !!!
"Later on the research team modified the microbial fuel cell by adding a third chamber between the two existing chambers. They also put certain ion specific membranes between the central chamber and the positive and negative electrodes. The ion specific membranes permit either positive or negative ions to pass but not both. Now they place salty water to be desalinated in the central chamber." I wonder what they used for membranes? I'll take a look at Logan's site and see if he's published anything on this. It's the first I've heard of this application or a 3 chamber cell. Thanks for the info
Idea on methane collection: Add a valved aquarium tube ended in an interface with attachable valved end connected to a lightweight &quot;bag&quot;. Put on empty - remove when full, vacuum empty, replace. Make 2 for efficiency.
a species of bacteria known as Methanobacterium palustre can convert CO2 to methane. will it work in this setup??
I'm not really a scientist, I just play one on instructables...-)<br> <br> Here's a link to the base article:<br> <br> <a href="http://pubs.acs.org/doi/abs/10.1021/es803531g" rel="nofollow">Direct Biological Conversion of Electrical Current into Methane by Electromethanogenesis</a><br> <br> I would recommend the Jello based design as a test platform. It is much more adaptable and a number of configurations can be tested at once. Current can readily be applied across the electrodes or through the media depending on the experimental model.<br> <br> If your goal is the production of methane I would suggest that you will get better results with an algae farm. There are numerous tank designs that will scale up extremely well. The energy input cost, even with pumps, is lower. The Chinese have reported ( in peer reviewed journals, see the Journal of Power Sources ) that get 1L of methane for each liter of algae sludge mixed with approximately 50% paper pulp.<br> <br> The sludge and pulp is placed into an anaerobic digester and the methane captured. The exhausted sludge is dried and used as a high grade fertilizer.<br> <br> All of these technologies are low-tech and within the grasp of virtually anyone.<br>
I want to make an electrolytic cell which uses carbon and produces methane as explained in this article: http://www.azonano.com/news.asp?NewsID=17238 The problem is that I don't know how to proceed with this idea. Some Help Please!
&nbsp;I'm a little confused as to exactly what &quot;silkscreen material&quot; means. If its a nonconducive mesh, how will the electrons produced by the anaerobic bacteria get to the cathode?
Silkscreen material is a fine mesh fabric used in silkscreening. It is inexpensive and readily available so it can be used to provide mechanical support to the bridge while allowing the free flow of electrolyte solution ( and the associated ions ) through the mesh.<br /> <br /> Without it the agar (or other salt bridge media) will break down and collapse quite rapidly (eventually it will completely degrade in any event). A mechanical support ( such as silkscreen material ) can delay that.<br /> <br />
&nbsp;Are there some alternatives I could use to replace silkscreen material?<br /> <br /> I'm not sure where exactly to go to get access to it. Also, should the agar be touching this material when its actually placed over the pipe?<br /> <br /> Sorry for taking your time.<br />
I'm always pleased to answer questions. There are many things you can try such as pantyhose material. Silkscreen material will be available at most art supply stores.<br /> <br /> I would place it over the end when I poured in the gelatin/electrolyte mixture,&nbsp; This will bind the agar and the mesh together.<br /> <br /> Also consider possibly cutting out a circle or two that will fit in the pipe and can be manipulated down onto the interior surface.<br /> <br /> You might try one or two without worrying about the mesh just to work out the rest of the process details and get an idea of expected voltages over, say, a week or two.<br />
what kind of voltage is it capable of putting out?
I got an update from a kid doing some classroom work. He's reporting .120V (maybe a typo) from 1-2 ml of E. Coli innoculant.<br/><br/><a rel="nofollow" href="http://groups.google.com/group/DIYbio-SF/browse_thread/thread/f2178d7f12c053a7">http://groups.google.com/group/DIYbio-SF/browse_thread/thread/f2178d7f12c053a7</a><br/>
That's a very good question. If you get a good answer please share it with the rest of us...:-) Current flow is going to be controlled by the bacterial population which is not optimized by sticking a pipe into a riverbed. I asked Dr. Logan about populations and he suggested a mixed population but didn't give me a detailed recommendation. I'm hoping to experiment a great deal in selectively breeding a population optimized for algae sludge by feeding them, well, algae sludge and let the best germs win... It's also not clear to me what the theoretical limits are, if any. A metal oxide battery/fuel cell has a theoretical max of 1.2V, I don't know if an MFC has a similar limitation or how far it can be scaled up. The folks at PS are wastewater specialists and speak glowingly of scalability but I haven't investigated that in any detail. I'm actually interested, at this point, in finding out what the cell volume/sunlight/nutrient ratio to determine the smallest functional cell that can be configured into a power grid is. Putting a bunch of them together is a sure fire way to scale up, but to what I cannot say at this time...
How has the methane been captured in the anode? In certain cases even carbon dioxide will be given out as a byproduct in the anode. How can these gases be obtained as an an output from the cell?

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