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Solubility Data
#1
Posted 05 April 2006 - 10:47 AM
Ive got to design a absorption column and to do part of my design i need to know the solubilty of so2 and nox in caustic soda and i cant find it anywhere! i was just wondering if anyone could help! thank you!
#2
Posted 06 April 2006 - 11:36 AM
Doug
#3
Posted 06 April 2006 - 01:17 PM
Doug
if equilibrium is reached. The mass transfer and kinetics can limit the amount that is absorbed. So there is no clear cut answer to the question - like you said.
#4
Posted 10 April 2006 - 08:12 AM
I'm a little confused by your talk of equilibrium. When you reach the point where you cannot absorb additional acid gases, you have exhausted your caustic and you no longer have an alkaline solution. I suppose that ideally you might strive to reach that point for the sake of maximum caustic utilization, but pH is a tricky thing and can swing rapidly fron high to low pH as you approach "equilibrium". Therefore, practically I don't think you'd ever get too close to a pH of 7. If you accept that, then you are always operating with an alkaline sorbent solution and you never reach solution/gas "equilibrium". You can reach steady state by operating the process continuously and setting a "blowdown or drawoff" flowrate to produce the desired solution pH. The desired pH would definitely be in the alkaline range.
Doug
#5
Posted 12 April 2006 - 12:25 PM
#6
Posted 14 April 2006 - 07:34 AM
Doug
#7
Posted 19 April 2006 - 02:56 AM
Concerning NOX, usually you have both NO and NO2 ; the partition depends on the upstream process. In incinération you have about 10% NO2 and 90% NO
NO2 is soluble in caustic, NO is not. To scrub NO you need an oxidizing agent, like sodium chlorite, hydrogen peroxide, ....
You will find a lot of litterature concerning NOx wet scrubbing.
Some people also use ozone of phosphorus to oxidize (in the gas phase) the NOx all the way to nitric acid.
If you plan to use caustic, keep in mind that at a high ph (>8.5) you'll start collecting the CO2, if any is present.
#8
Posted 19 April 2006 - 08:04 AM
Doug
#9
Posted 19 April 2006 - 12:23 PM
no there is no CO2 in my absorption column. Only NOx and SOx. The NOx and SOx are quite dilute and make up about 17% of the incoming gas the rest is steam. Does this mean i can still consider it to be total absorbtion in my column?my tutor said that for my equilibrium line i should look at the solubilty of nox and sox in water as they react with the water first and then with caustic soda and the reaction with the water is the rate determining step-is this correct? Thank you for you help.
#10
Posted 20 April 2006 - 09:54 AM
If you are using caustic you cannot calculate the absorber based on the SO2 (or NO2) solubility, because the reaction SO2 + NaOH --> NaHSO3 or Na2SO3 (depending on pH) is a very fast reaction, that will speedup the transfer. (refer to Perry's handbook for the basics, see enhancement factor)
You may have two limiting factors
the gas side mass transfer coefficient (at low concentrations)
the liquid side mass transfer coefficient (at high SO2 concentrations, for example)
so in a such case you need to worry about both sides, liquid and gas.
Since NO is barely soluble and will not readily react with NaOH, you may use solubility data to calculate your equilibrium line and select your operating line.
For SO2, at a pH high enough (say > 7) there is almost (almost) no SO2 as such in the liquid phase. so the equilibrium line is almost flat, and the only controlling parameters will be the kg.a and kl.a . The main criteria for selecting L/G would then be how concentrated you would allow the bleed to be (obviously less than saturation)
for NO2, the solubility is limited, but there will be some enhancement because of reaction with NO2
Are you a student?
If your need more help, please supply the actual flowrate, full composition incl. concentrations of NO / NO2 / SO2 , and temperature / pressure , along with specifications
I think that you'll need more than caustic if you have much NO (nitrogen monoxide)
#11
Posted 21 April 2006 - 05:45 AM
my flow rate going into my absorption column is 3652.707 kg/hr and 88% of it is steam, 1.5% is SOx and 10% is NOx. is this a very concentrated stream? also do you know how much nox and sox i am legally allowed to give off in my plant? im still a little bit confused about what i have to do for my equilibrium line. thank you so much for your help!
#12
Posted 21 April 2006 - 08:38 AM
, not lumped together as NOx
T and P were not supplied, also
#13
Posted 21 April 2006 - 09:14 AM
#14
Posted 27 April 2006 - 06:22 AM
In your case, I do not have enough information to advise what would be best.
Now, I will not discuss this matter any further if you don'nt give the full composition, including NOx speciation.
#15
Guest_Jonathan_*
Posted 30 April 2006 - 06:31 AM
I have recently begun working for a company that often has cause to design packed beds to reduce NOx emissions. They are acid plants so I guess NO will get oxidised and this is why we always refer to it as NOx and dont consider the make-up.
I am having problems with design of these columns though - I thought we might be able to share our information. The reaction takes place in the liquid phase and can be considered fast and irreversible. The limiting step is the adsorption to the liquid and so you need to use the Kga value for working out the height per transfer unit. Because it's a fast irreversible reaction you can consider the operating and equilibrium lines to both be straight. This means that you can calculate the number of transfer stages by just ln (y1/y2) where y is the gas conc in and out respectively. If you want i can e-mail a pdf of my source.
Emission limits depend on where the plant is - In China for example you can emit a lot compared to UK. We tend to be working on ppm though.
What this is leaving me with is the question of Kga values - where can I get these from for these scrubbers??
#16
Posted 03 May 2006 - 02:35 AM
Reinhardt Billet 's Packed tower ISBN 3-527-28616-0 has lots of useful correlations for Kl.a Kg.a and holdup in packed towers
#17
Posted 15 November 2006 - 12:14 PM
I too am designing a scrubber for HCl, SO2 with NaOH scrubbing. Now my question is: what is the pH needed to say that the reactions in the scrubber are irreversible, meaning NTU = ln(y1/y2)?
And, should I measure that pH at the flow out side of the liquid of the bottom of the scrubber?
Also, is it common for scrubbers that your G to L ratio is constant?
Thanks
Albert
#18
Guest_arvind.che_*
Posted 18 May 2007 - 06:00 AM
Doug
if equilibrium is reached. The mass transfer and kinetics can limit the amount that is absorbed. So there is no clear cut answer to the question - like you said.
you have told about the mt and kinetics . is there no possibility to generate the chemical dat by vle experiment.if i am wrong then plz guide me
#19
Posted 13 October 2009 - 12:26 AM
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