How to turn plastic waste into diesel fuel cheaply

[Excalibur]

My pyrolysis is essentially how Wheels described his, a series of pots, which function, like Excalibur's description of the "doubler" in the distillery. I also have a pot for each cut as well.

However, the downside, as Excalibur pointed out, is more heaters, more heat, but a lot more control, because all of my heaters are electric, which gives greater control.

The result is my product ranges from clear to amber.

[wheels]

My more heaters, more heat, but a lot more control, because all of my heaters are electric, which gives greater control.

The result is my product ranges from clear to amber.

Yes the only way to do it in my opinion. The more control results in a more precise output range of Hydrocarbon.
I have electric heating on all my pots, but so far have no used them. This is only because from the Catalyst onwards, my Plant takes a slightly different track than everyone else. Although my catalyst cracks, the main reason for it to be there is for removal of a specific chemical that is used in all Ewaste plastics as a fire retardant. If that is not removed, it causes all sorts of corrosive issues and is very toxic. Plus it retards combustion of the Fuel in the Burner. It will do the same in an engine and for such a reason, I have not gone too far down the path of using my Fuel in an engine just yet. I have done it to test if it works, but I need to do a great deal more work in that area to understand long term issues that may or may not arise. Anyway....
back to the story. So my Catalyst is heated to a very high temperature to initiate the conversion process and then the Vapor stream needs to be cooled dramatically before reaching the First Pot. But what I have found is that the Vapor arrives at the first pot at a suitable temperature and so I do not need to heat it again. A bonus because it save energy heating the Pot. That captures any heavy fractions and the vapor is allowed to flow to the second pot, where I am trying to rapidly get it down to a much cooler temperature before any "solvent" ranges flow on to the Chilled pot. If I allow to much heat to flow on into the Chilled pot, then the chiller can not cope and it gets too warm and I end up with a very light fuel floating on top of the bubbler water.
I am currently working on a new feed design and that will allow the continual feeding of the plant along with being able to process multiple plastic types separately, yet simultaneously and each type can have a particular process applied to meet their individual need. But it will result in a wider ranging hydrocarbon output that will need greater effort in cracking and containing.

[Beyond Biodiesel]

My pyrolysis is essentially how Wheels described his, a series of pots, which function, like Excalibur's description of the "doubler" in the distillery. I also have a pot for each cut as well.

However, the downside, as Excalibur pointed out, is more heaters, more heat, but a lot more control, because all of my heaters are electric, which gives greater control.

The result is my product ranges from clear to amber.

[Excalibur]

[wheels]

Ever notice how the 2nd condenser distillate is always cleaner and clearer?

Yes and that also fits my my thoughts on the Molecular length grabbing particulates and carrying them through. The second pot will have far shorter chains.
By the way, Viscosity can be linked to chain length, although in theory, it is a lot more complex than that.

[Excalibur]

Rozier, I would put another TC here....

This TC would be connected to a temperature controller that keeps retort temperature within a predetermined range.

I think that even in an industrial distillation plant there'd be some degree of particulate carry over. Ever notice how the 2nd condenser distillate is always cleaner and clearer? The object is to gently, gently heat the feedstock, holding it within a tight temperature range. Avoid hurrying/bullying the boiling process because it leads to a poorly distilled product. It's the operators job to find the retort temperature point that gives good flow but excludes excessive particulate carry over. The rule is: higher temperature is not always better. It's a balance between the 2 parameters.

Keep talking and sharing ideas..

[wheels]

I have noted that when we run plastic or oil there is always what i call, small black carbon carry over. We now filter out that at end of process. Due you also have this happen in your machine?
Thanks Folks.

Yes. And to be honest, I don't know why apart from assuming it is because of the viscosity of the Hydrocarbon being vaporized. My Plant processes ABS Plastics (don't try this anyone, the stuff is toxic, corrosive and difficult to process) and ABS is full of Plasticizers. Mostly Clay. It is silky smooth fine clay particles and it all comes through the process to the end fuel. The only way to remove it is centrifuge, because the particles are so fine, they go straight through filters, or at the least, plug them instantly. So it is not always because of boil over. I have a feeling it could be because a Fuel/oil molecule is long enough that it can partly wrap itself around very fine particles. And we are talking particles fine enough to go right through filters, so they are at least less than 5micron in size. A Centrifuge will take particles down to 0.1 of a micron. But it is a long slow process of cycling the Fuel till it is clean.

[rozier56]

rozier56

Tanks for your comments.
Need to point a few points of info.
Wheels the inner basket shown in the distillation column is actually filled with baffle materials, ie. mild steel bolts and packed tightly providing good surface area for distillation.
The reduced flow pipe that Excaliber has from the distillation to the condenser i believe will slow down the gas outflow escaping from the distillation to the condenser.Because the system is open ended, it wont necessary cause a back pressure but must influence flow rate to the condenser. If one looks at most moonshine stills depicted you will see they have a similar design.I believe this allows better condenser operation. The other option is to go with bigger/longer condenser. I am going to try Excaliber style first to see the result.
Excaliber my temp probe on the distillation column is on top of the right bend before going to condenser.We ran that oil run at 360*c at distillation.
I also found out that the sample sumitted was actually taken from my plant sample point prior to filtration, hence high impurities.{not to smart}
I have noted that when we run plastic or oil there is always what i call, small black carbon carry over. We now filter out that at end of process. Due you also have this happen in your machine?
Thanks Folks.

[Excalibur]

Diesel report on some truck engine oil that we converted.
WOULD APPRECIATE YOUR COMMENTS!
NO CATALYST USED.

[wheels]

A word pf caution re the Sulphur content. DO NOT use sulpher rich fuels in modern Vehicles that have Catalytic converters in the Exhaust system. Many modern Diesels now have thee for No2 emmision control and Sulphur simply blocks them up and renders them useless.

[Excalibur]

Excaliber, attached is a drawing of my retort,reflux and the condenser.
Note the condenser is the same size of reflux outlet.I believe this system allows to much gas outflow through the condenser and results in too much outflow not condensed through the exhaust. This will affect through put and quality.
Noticed on your system that you have a lead pipe of 40mm, leading to the condenser.Surely this will slow down the gas outflow from reflux,allowing better condenser conditions.This will also create a little back pressure on the system enhancing the reflux performance.
What is the length of that pipe connecting the reflux to the condenser.
Note my reflux outlet is 80mm diam and so is the condenser inlet. I have 8 smaller pipes in the condenser for gas cooling.

Nice drawing! The length of pipe is nearly 3m. I don't consider the pipe diameter to give any significant or undue back pressure.
The condenser needs to be able to condense all condensable vapors passing through under all conditions. If condensable vapors are escaping out the end, it is either not efficient enough or simply not big enough.

It's great to get a lab test on your diesel.
Low flashpoint is too much volatile content. Hold the diesel at a temperature that allows those volatiles to evap off. I suggest do this on the fly while/as the product is made.
Contaminants could benefit from filtering or possibly are the result of a system that is being driven too hard. Where retort boiling is too vigorous, the reflux becomes overwhelmed and contaminants are allowed to flow downstream. Then it is not proper distilling. Distilling/cracking requires careful adherence to temperature control. The retort contents will behave nicely if it is run at a pace it is happy with. Forcibly hurrying it will result in undistilled product with contamination. It would be better to use good distilling practices than it would be to have to clean up poorly distilled product afterwards.
I think we are stuck with sulphur content (but at least we are recycling!).

[wheels]

Diesel report on some truck engine oil that we converted.
WOULD APPRECIATE YOUR COMMENTS!
NO CATALYST USED.

Several things. Firstly, the fuel has a lot of contamination. You need much better filtration. You can also leave the Fuel to settle for a week or so in a large tank, then either pump off the top of the tankful or pour off the bottom. Fine particles will tend to go right through Fuel filters. The best form of filtration is Centrifuge and keep cycling the Fuel over and over.
Sulphur content is very high and needs removing from the fuel. But It is very hard to remove Sulphur. It requires a complex Hydrogenation/Catalytic process.

[wheels]

Excaliber, attached is a drawing of my retort,reflux and the condenser.
Note the condenser is the same size of reflux outlet.I believe this system allows to much gas outflow through the condenser and results in too much outflow not condensed through the exhaust. This will affect through put and quality.
Noticed on your system that you have a lead pipe of 40mm, leading to the condenser.Surely this will slow down the gas outflow from reflux,allowing better condenser conditions.This will also create a little back pressure on the system enhancing the reflux performance.
What is the length of that pipe connecting the reflux to the condenser.
Note my reflux outlet is 80mm diam and so is the condenser inlet. I have 8 smaller pipes in the condenser for gas cooling.

You do NOT want back pressure of any amount. In fact if we could easily create a vacuum, while the process is working, that would be even better.
Condensing the Vapor is about cooling it as fast and efficiently as possible. The speed of the vapor traveling through needs to be slow. So a large condenser diameter is better than a small one. If you have uncondensed vapor making its way through to the bubbler, then you need more cooling.
Everything works on temperature, not speed of vapor. The reflux MUST be held at the right temperature to condense the heavy vapor and have it return to the Retort. I dont think you need the inner jacket or whatever it is. 'That will stop the vapors from having free access to the reflux vessel wall, where the gas is condensed.

[wheels]

Pics of rope?

The orange rope is PP. It is a little harder to see the white rope on my screen, but I think they are both PP. Do they both feel the same?

[rozier56]

rozier56

Diesel report on some truck engine oil that we converted.
WOULD APPRECIATE YOUR COMMENTS!
NO CATALYST USED.