Membrane separations experimental set up

In summary: The figure in your OP is just for one module (co-current flow). It includes the whole lab manual so I don't have to just give you vague details without anyone knowing the whole context of the experiment.In summary, the objective of the experiment is to determine the membrane selectivity to oxygen from measurements of the membrane transmissibility to nitrogen and oxygen. The model will predict the dependence of permeate flow rate and purity on the retentate production rate, pressure, and composition, as well as the membrane transmissibilities.
  • #1
gfd43tg
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Hello,

I will be doing an experiment to separate N2 from O2 in air using membrane separations. I need to write my own experimental procedure to find the objectives of the experiment.

OBJECTIVES:
i. Determine the membrane selectivity to O2 from measurements of the membrane transmissibility to N2 and O2.

ii. Characterize the membrane to determine how air-separation performance depends on feed pressure, retentate flow rate, and module configuration (i.e., co-current or counter-current).

iii. Develop a mathematical model to predict the dependence of permeate flow rate and purity on the retentate production rate, pressure, and composition, as well as the membrane transmissibilities. Discuss model limitations.

iv. Based on the experimental and model results, recommend optimal operating conditions (pressure, flow rate, module configuration) to produce a >95 mol% N2 product stream. Describe tradeoffs in operating conditions.

Here is our experimental set up

upload_2015-10-3_14-53-4.png


I'm trying to figure out how to do objective i. I need to figure out the selectivity of the membrane for oxygen over nitrogen. It says I should calculate the transmissibility of the two species. the transmissibility, ##k_{pi}## is defined
$$ k_{pi} = \frac {\mathcal{P}_{i}}{L_{m}} $$

Where ##\mathcal{P}_{i}## is the permeability of species ##i##, and ##L_{m}## is the length of the membrane. You can calculate the molar flux, ##J_{i}##

$$ J_{i} = k_{pi}(P_{ir}-P_{ip}) $$

Where ##P_{ir}## is the retentate pressure (feed pressure), and ##P_{ip}## is the permeate pressure. I get I can find the feed pressure from the first gauge, but from the diagram there is no pressure gauge for the permeate. I figured I could calculate the molar flux because the permeate flow rate is equal to the area of the membrane times the average molar flux

$$ V_{p} = A_{T} \langle J_{i} \rangle $$

So I could use the rotameter to find ##V_{p}##, then knowing ##A_{T}## I can calculate the ##\langle J_{i} \rangle##. Once I have ##\langle J_{i} \rangle##, I would do

$$ \langle J_{i} \rangle = k_{pi}(P_{feed}-P_{permeate}) $$

But I run again into the problem of not knowing ##P_{permeate}##. If I can get that, then I know the selectivity is trivial

$$ \alpha_{ij} = \frac {k_{pi}}{k_{pj}} $$

Any ideas how I might be able to do this? One thought is using the temperature of the permeate to find the permeate pressure with the ideal gas law.
 
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  • #2
As you release the filter products into the air again without additional pumps, I would expect a pressure close to atmospheric pressure behind the membrane (no needle valve at the middle line).
 
  • #3
I read on wikipedia that a needle valve is used for precise flow measurements. How does that relate to your expectation of a pressure neat atmospheric pressure?
 
  • #4
It is unrelated because my comment refers to the line without it.
 
  • #5
Right, but I'm interpreting your meaning as the lack of a needle valve implies atmospheric pressure. If this is the correct interpretation, I'm curious how that is so.
 
  • #6
I don't see anything that could change the pressure. It's basically an open pipe.

The needle valve can maintain a pressure difference between its sides.
 
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  • #7
Okay, sounds good. Thank you! I will come back if I get stuck on the other objectives.
 
  • #8
I have to admit, something strange in the lab manual procedure

Downstream of the toggle valves, a pressure gauge indicates the inlet (feed) pressure. After passing a pressure-relief valve set at 100 psig, a thermocouple measures the inlet temperature. The temperature console enables measurement of either the inlet or permeate temperature. Note that the temperature measurements are necessary for determining the molar flow rate of permeate.

I don't understand why I would need the temperature to determine the flow rate of the permeate if I have a flow meter, as seen in the diagram. Here is an overall diagram. The one I posted earlier is just for one module (co-current flow). I included the whole lab manual so I don't have to just give you vague details without anyone knowing the whole context of the experiment.

upload_2015-10-3_18-59-58.png
 

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  • #9
Density depends on temperature and pressure. I don't know your flow meter, if it just measures volumetric flow you need the density of the medium to calculate mass flow.
Even it measures mass flow directly, its measurement will still depend on temperature a bit. Better flow meters have internal thermometers and software to correct for that.
 
  • #10
This bit of information may help from the lab manual
Permeate
Permeate flow rate is indicated on a rotameter and is measured by a dry-test gas meter. The dry-test gas meter is highly accurate and registers total volume in ft3 (note: this is not the volume at STP). To measure permeate flow rate, use a stopwatch to make timed-volume measurements with the dry-test gas meter.

I figure I will read from the rotameter the volume and divide by time to get volumetric flow rate. Then I need the temperature to know the density of the gas. From the figure in my OP, what's the purpose of having both a rotameter and a flow meter?
 
  • #11
Maylis said:
Then I need the temperature to know the density of the gas.
And pressure. Yes, that's the point.
Maylis said:
From the figure in my OP, what's the purpose of having both a rotameter and a flow meter?
I don't know.
 
  • #12
Turns out the volumetric flow meter range is too small, so it maxes out even at small flow rates
 

1. What is a membrane separation experimental set up?

A membrane separation experimental set up is a laboratory technique used for separating mixtures of substances using a semipermeable membrane. This method relies on the differences in the size, charge, and solubility of particles to selectively allow certain substances to pass through the membrane while blocking others.

2. What are the different types of membranes used in membrane separation experiments?

There are three main types of membranes used in membrane separation experiments: reverse osmosis membranes, ultrafiltration membranes, and nanofiltration membranes. These membranes have different pore sizes and are used for different types of separations based on the size and properties of the particles being separated.

3. What factors should be considered when setting up a membrane separation experiment?

Some important factors to consider when setting up a membrane separation experiment include the type and properties of the membrane being used, the properties of the substances being separated, the operating conditions (such as pressure and temperature), and the flow rate of the solution being separated.

4. How is the performance of a membrane separation experiment measured?

The performance of a membrane separation experiment can be measured by calculating the separation efficiency, which is the ratio of the amount of desired substance that passes through the membrane to the amount of undesired substance that is rejected by the membrane. Other factors such as flux rate and selectivity can also be used to evaluate the performance of a membrane separation experiment.

5. What are some common applications of membrane separation experiments?

Membrane separation experiments have a wide range of applications in various industries, including water treatment, food and beverage production, pharmaceuticals, and biotechnology. They can be used to purify water, concentrate liquids, and separate proteins, enzymes, and other biomolecules from a solution.

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