I recently started a career as a chemical engineer and was assigned to design a purfication system for a ABE fermentation. At the distillation step of my purfication process I decided to use 1" metal Pall rings in my column. I found the column to be about 1 foot in diameter and the packing height to be about 14 ft tall. I wanted to know if I need a column the same height as the packing height or should the column be slightly larger than the packing height of 14ft and why?
Thanks
WorkingBugs
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Calculating Distillation Column Height
Started by Guest_workingbugs_*, Feb 09 2011 04:19 PM
6 replies to this topic
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#1
Guest_workingbugs_*
Posted 09 February 2011 - 04:19 PM
#2
Posted 09 February 2011 - 05:09 PM
WorkingBugs:
I am not knowledgeable in the Acetone-butanol-ethanol (ABE) fermentation process, but I do know a little about packed distillation towers. I dont believe you should be trying to use 1 Pall rings in a 12 ID distillation column. If I had to use my guessing cap, I would say you should apply a ½ or 5/8 size of Pall ring. I havent the calculations to back me up, but my suspicion is that the 1 size ring will not give you enough contact space and your HETP will be very high and that is not even taking into consideration that you will suffer a lot of by-passing and channeling. Have you checked your decision with the experts the fabricator and supplier of your Pall rings? I certainly recommend you get in contact with your proposed packing supplier and make sure of your selection. Note that I highlight the word YOUR. That means that you are taking ALL THE RESPONSIBILITY for the resulting performance of the distillation performance. I would not recommend you do that unless you are collecting the commensurate amount of monies to justify that risk.
You dont have the experience in having done this type of design and implementation work before, so Ill make some unsolicited recommendations for you to ponder:
- I assume that you are working at the production plant level and that you are to design and have a purification train built for separating the feed Acetone, Butanol, and Ethanol. I have to do this since you have given us zilch input or scope of work information. If so, you should specify what you want to separate to a packing manufacturer who can work with you and help with the packing design.
- To do the above, you have to pre-select a packing supplier and that is what you should do first.
- Have the packing supplier supply all the packing, supports, distributors, and re-destributors required by the packing supplier's own design. Try to have the packing supplier assume the responsibility for the performance expected and be prepared to supply him/her with all the required basic data and backup information. Do not take that liability yourself - unless you are independently wealthy.
- Make sure you allow for the recommended bed spacings and heights. You will require multiple beds withing the same tower, so make sure you allow for packing removal at the bottom of each bed and packing introduction at the top of each bed.
- Make sure you allow for sufficient tower sump capacity. For a 12 tower I would allow for at least 3 feet of sump height. I would allow a minimum of 12 between beds for distribution and access. I would allow 24 above the top bed for disengagement space. I would estimate that each bed would be about 56 tall, making it 3 packed beds in the tower.
- Based on the above, I estimate the over-all tower to be (3+14+2+2) = 21 feet tall and that doesnt include the tower support skirt that is needed, assuming you used a thermosyphon reboiler. I estimatel the skirt would add another 6 feet, making the total tower height 27 ft twice the height of your packed beds. A tower this thin with a 27:1 L/D ratio is going to require substantial structural support - don't forget that you will need platforms and access ladders to inspect, dump, and load packing. You will also need lighting.
I hope this helps.
#3
Posted 09 February 2011 - 07:52 PM
Hi
Agree with Art's line of thought, just my 2 c
- try to keep the column dia around 500-600 mm and not less, you will have wall effects that affects the column performance.
- working from the above dia, suggest you check what packing will give you reasonable flood at max-min flow. this includes turndown and startup conditions
- most important, choose the right material for your system and a packing type/size that will not easily foul (pall rings have good fouling resistance in general)
- your manway size depends on your column internals size, inspection needs and column dia. you cant have a manway in a 300 mm, its going to be too small "a hand hole"
would suggest you have a read at H Kister books on distillation design & operation, you will find all you need there including design guidelines. also as Art suggested, try to use your internals vender and best to talk to few
cheers,
SM
Agree with Art's line of thought, just my 2 c
- try to keep the column dia around 500-600 mm and not less, you will have wall effects that affects the column performance.
- working from the above dia, suggest you check what packing will give you reasonable flood at max-min flow. this includes turndown and startup conditions
- most important, choose the right material for your system and a packing type/size that will not easily foul (pall rings have good fouling resistance in general)
- your manway size depends on your column internals size, inspection needs and column dia. you cant have a manway in a 300 mm, its going to be too small "a hand hole"
would suggest you have a read at H Kister books on distillation design & operation, you will find all you need there including design guidelines. also as Art suggested, try to use your internals vender and best to talk to few
cheers,
SM
#4
Posted 10 February 2011 - 09:49 AM
Hello all
I agree, for the most of it with what has already been said. I disagree that 500-600mm is a diameter under which a design should not be made.
My comments:
Pall rings are no longer state of art packing, and you should be able to find more efficient packing (better price/efficiency/capacity compromise)
1" nominal size in a 12" ID column is bit outside of the recommendations, but is no way completely unnacceptable. You just have to take into account additional wall effects. Yet I'd prefer 5/8" nominal size. I have seen many industrial columns in the 250-500mm diameter range.
I would seriously consider a structured packed column.
I have not found any information indicating how you reached the 12" ID and the 1" pall / 14' deep bed. I have designed and run colmuns not larger than 300mm ID (10') without problems. Of course insulation is critical.
When you dump the packings into the column, special care is needed.
No water in the feed?
I agree, for the most of it with what has already been said. I disagree that 500-600mm is a diameter under which a design should not be made.
My comments:
Pall rings are no longer state of art packing, and you should be able to find more efficient packing (better price/efficiency/capacity compromise)
1" nominal size in a 12" ID column is bit outside of the recommendations, but is no way completely unnacceptable. You just have to take into account additional wall effects. Yet I'd prefer 5/8" nominal size. I have seen many industrial columns in the 250-500mm diameter range.
I would seriously consider a structured packed column.
I have not found any information indicating how you reached the 12" ID and the 1" pall / 14' deep bed. I have designed and run colmuns not larger than 300mm ID (10') without problems. Of course insulation is critical.
When you dump the packings into the column, special care is needed.
No water in the feed?
#5
Guest_workingbugs_*
Posted 11 February 2011 - 08:24 AM
Sorry about the lack of information. Let me try and clear some things up. We are trying to scale up this process from the 500 gal scale to the 4000 gal scale. As of right now our distillation purification step for distillation is outsourced to a local distillery that we have relations with. My job is to make the process in-house. My goal is to have the stripped vapors of water and butanol (trace ethanol and acetone) from the fermentation condensed and fed into a decanter. The decanter then feeds to two columns (a butanol and a water column) the bottom products would be butanol and water out of their respective columns with the overhead vapors being that of all the components due to the azeotropes. The overhead vapors would then be condensed and fed back to the decanter until the desired separation is achieved. As for sizing the column, I did this by guide from 'Separation Process Principles' By Seader and 'Plant Design and Economics for Chemical Engineers' By Peters and Timmerhaus for packed column Design. The height I got for packing was by advice from someone at the distillery who uses ~12 trays to do what we need (I also read a paper that said this exact feat could be accomplished with 10 trays) and then I used the HETP method and guidelines of HETP=Dt if Dt < .5 m for the packing height. I have not talked to any random packing suppliers yet. This was my first stab at this and I wanted to get some prices for things so I can put together a quick economics flow sheet to present to my boss. If you need anything else to give me any advice, please don't hesitate to ask and I will try my best to furnish you with the information.
Regards
WorkingBugs
Regards
WorkingBugs
#6
Posted 11 February 2011 - 10:29 AM
WorkingBugs:
Congratulations. You are now doing the smartest thing a young chemical engineer can do in your present situation: define and evaluate what you have as a scope of work and start to identify your work path and resources. Your lack of experience immediately should lead you to consult with those that you can identify as having the experience that you lack and using them as your starting resource. And in order to maximize the effectiveness of that kind of resource you have to make sure that you pass on all the basic data and scope to your resources in order to make sure you receive their maximum, usable, and correct input. That is where good communications come into play.
I have been in similar situations when I was a young graduate and so, will take this opportunity to emphasize some valuable inputs that you have already received and that, in my opinion, you should heed:
- Confirm and make sure your estimates for the Packed bed height is correct. As I stated, you may be able to use a packing supplier to work with you on this application. By making sure that this first step is correct, you can then verify the estimated overall height required for the distillation column and accessories. This is important because this is the largest part of the total investment.
- What Siretb seriously recommends as a structured packed column may be the smartest solution to effecting a good separation with the shortest overall height. Again, this can be verified with the right packing manufacturer and your knowledge of the cleanliness of your feed strea
- Bear in mind that structured packing may not work out with a small diameter column (12 or even 24 ID) without having to have body flanges on the column which adds costs and introduces flange leaks and maintenance. Again, this is another point to work out with a packing supplier.
- Finalize your decision on what kind of reboiler you intend to use. This may also impact on the overall height. This also applies to your overheads condenser and reflux requirements.
- As both Siretb and Smalawi advise you, be careful and fully aware that wall effects, fouling, channeling, and good distribution become very important subjects when you deal with small diameter packed columns. The perfect perpendicular position of the column and its internal liquid distributors becomes very important especially in relatively tall, slender columns. This is why I caution you on making sure you allow for any required structural steel that may be needed to reinforce the column integrity and alignment as well as personnel access.
What we need from you in order to help you is ALL the basic data and scope of work you can feed the Forum. Without that, we cant offer suggestions, comments, advice, or recommendations. I hope we can help you further and out Forum has always served as way station to those that seek help.
Hope to continue to hear from you.
#7
Guest_workingbugs_*
Posted 11 February 2011 - 04:10 PM
Thanks Art,
What I have up to this point is the mass and energy balance leading into the columns. Into the butanol column I have an inlet temp of 34 C. There is 28 kg/day of water, 138 kg/day of butanol, 6.9 kg/day ethanol, and 3.5 kg/day acetone. The distillate has a butanol water ratio of 3 and a total flow of 120 kg/day assuming all ethanol and acetone go to the distillate. The Bottoms is 1% water the rest being butanol. For the water column the feed is 372kg/day water, 44 kg/day butanol,17 kg/day ethanol and 9 kg/day acetone. This time all the butanol goes to the top of the column and again the butanol water ratio is 3. The rest of the water goes to the bottoms and is used elsewhere. The acetone and ethanol again go to the distillate. The distillate rate is 84 kg/day. The distillate temperature of the butanol column should be around 71 C and the bottoms temp should be around 98 C with the column running at 93 C (the boiling point of the butanol/water azeotrope.) The water column is also run at 93 C with the Distillate temp being around 69 C and the Bottoms at 81 C. I hope this information helps.
What I have up to this point is the mass and energy balance leading into the columns. Into the butanol column I have an inlet temp of 34 C. There is 28 kg/day of water, 138 kg/day of butanol, 6.9 kg/day ethanol, and 3.5 kg/day acetone. The distillate has a butanol water ratio of 3 and a total flow of 120 kg/day assuming all ethanol and acetone go to the distillate. The Bottoms is 1% water the rest being butanol. For the water column the feed is 372kg/day water, 44 kg/day butanol,17 kg/day ethanol and 9 kg/day acetone. This time all the butanol goes to the top of the column and again the butanol water ratio is 3. The rest of the water goes to the bottoms and is used elsewhere. The acetone and ethanol again go to the distillate. The distillate rate is 84 kg/day. The distillate temperature of the butanol column should be around 71 C and the bottoms temp should be around 98 C with the column running at 93 C (the boiling point of the butanol/water azeotrope.) The water column is also run at 93 C with the Distillate temp being around 69 C and the Bottoms at 81 C. I hope this information helps.
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