Question

In: Chemistry

An ion exchange column containing 99.3 g of amberlite ion exchange resin was used to remove...

An ion exchange column containing 99.3 g of amberlite ion exchange resin was used to remove Cu2+ from a solution where Co = 0.452 M CuSO4. The tower height = 30.5 cm and diameter =2.59 cm. The flow rate was 1.37 cm3 solution/s to the tower. The breakthrough data are shown below:

Time (s)                                 C [ g Cu mol/L ]

420                                            0

480                                           0.0033

510                                          0.0075

540                                          0.0157

600                                          0.0527

660                                           0.1063

720                                           0.1433

780                                          0.1634

810                                          0.1722

870                                           0.1763

900                                           0.180

The concentration at desired breakthrough is C/Co = 0.010.

Determine the following:

1.1 The breakthrough time.

1.2 Fraction of total capacity used up to the breakthrough point.

1.3 Length of unused bed.

1.4 Saturation loading capacity of the solid adsorbent.

NB: Units of C/Co is gmol/L

Solutions

Expert Solution

First calculate the value of for every concentration.

Then make a curve between times v/s C/Co

The breakthrough time from the curve can be calculated around = 490 seconds. ( The point where C/Co = 0.010)

(1.2) Total or stoichiometric capacity of the packed bed =

The time equivalent to the usable capacity of the bed up to the break-point time is =  

Hence, the fraction of total capacity used up to the break-point is

(1.3) Length of unused bed =

(1.4) Saturation loading capacity of the solid adsorbent =

To determine the saturation capacity of the carbon, air flow rate is

Density of

Totoal alcohol adsorbed is


Saturation capacity is


Related Solutions

An ion exchange column containing 99.3 g of amberlite ion exchange resin was used to remove...
An ion exchange column containing 99.3 g of amberlite ion exchange resin was used to remove Cu2+ from a solution where Co = 0.452 M CuSO4. The tower height = 30.5 cm and diameter =2.59 cm. The flow rate was 1.37 cm3 solution/s to the tower. The breakthrough data are shown below: Time (s)                               C [ Cu mol g]/L 420                                         0 480                                    0.0033 510                                      0.0075 540                                       0.0157 600                                         0.0527 660                                           0.1063 720                                            0.1433 780                                           0.1634 810                                              0.1722 870                                              0.1763 900                                               0.180...
Explain how to use an ion exchange column containing carboxymethyl resin to separate a protein mixture...
Explain how to use an ion exchange column containing carboxymethyl resin to separate a protein mixture containing insulin (pl = 5.4), hemoglobin (pl = 7.1) and cytochrome c (pl = 10.6).
An anion-exchange resin can be used instead of the cation-exchange resin in this experiment to separate...
An anion-exchange resin can be used instead of the cation-exchange resin in this experiment to separate the three amino acids in the known mixture. What changes to experimental protocol are required to achieve complete resolution? Support your response with an explanation. (HINT: consider pH). You have been provided a mixture containing four amino acids (Glu, His, Pro and Lys) to be separated by ion-exchange chromatography using a Dowex 50 cation-exchange, prepared in a loading buffer at pH 2.0. The following...
Silver ion, Ag+, can be recovered from photographic solutions by adsorbing onto an ion exchange resin...
Silver ion, Ag+, can be recovered from photographic solutions by adsorbing onto an ion exchange resin (Langmuir adsorption) Ag+ +Ex↔ Ag-Ex logKL =12.30 (where Ex represents an adsorbing site on the resin). According to the manufacturer, the resin has 1.20 x10-5 moles of adsorbing sites per gram of resin. a) If you have a liter of solution with [Ag+] = 0.030 mM, how much resin will you need to adsorb all the silver assuming 100% binding? b) Calculate the predicted...
A gas stream containing 3% A is passed through a packed column to remove 99% of...
A gas stream containing 3% A is passed through a packed column to remove 99% of A by absorption in water. The absorber will operate at 25 C and 1 atm, and the gas and liquid rates are to be 20 mole/h ft2 and 100 mole/h ft2 respectively. Mass transfer coefficient and equilibrium data are as follows: y* = 3.1 x at 25 C k_xa = 60 mol/h ft3 unit mol fraction k_ya = 15 mol/h ft3 unit mol fraction...
what is charge of the cationic exchange beads? which protein comes off the ion exchange column...
what is charge of the cationic exchange beads? which protein comes off the ion exchange column first?( Use the charge on the protein? Why does the second protein come off with 2M NaCl? Is there another possible way of removing the second protein from the column? Both of the proteins used here are colored. How could we separate proteins that were colorless or white Where is myoglobin found? what is its function? Explain how ion-exchange chromatography works? Why might you...
Ion-Exchange Column: You condition the column with 6 M HCl. Before you transfer the unknown to...
Ion-Exchange Column: You condition the column with 6 M HCl. Before you transfer the unknown to the ion-exchange column you need to wash the column until pH is above 6. Why?
how to calculate affinity column recovery and ion exchange recovery in LDH lab?
how to calculate affinity column recovery and ion exchange recovery in LDH lab?
Explain a different way of eluting a second protein in an ion-exchange column (other than by...
Explain a different way of eluting a second protein in an ion-exchange column (other than by the addition of salt). Explain why this method is not often used with proteins.
A mixture of three proteins shown below was applied to an ion-exchange column with CM-Sepharose as...
A mixture of three proteins shown below was applied to an ion-exchange column with CM-Sepharose as the stationary phase. Predict the order of elution of the proteins at neutral pH, assuming that the mixture was applied at low ionic strength and eluted with buffers of increasing ionic strength. Explain. Cytochrome c (12.0 kDa, pI = 10.6) Phosphofructokinase 1 (34.1 kDa, pI = 6.64) Bovine serum albumin (66.5 kDa, pI = 4.70)
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT