An Analysis of Sodium Bicarbonate [PDF]

In last week's laboratory, we synthesized Sodium Bicarbonate (NaHCO3) from Sodium Chloride. (NaCl) via the old ... Ammon

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CHEM 121L General Chemistry Laboratory Revision 2.2

An Analysis of Sodium Bicarbonate In last week’s laboratory, we synthesized Sodium Bicarbonate (NaHCO3) from Sodium Chloride (NaCl) via the old Solvay Process. NaCl(aq) + NH3(aq) + CO2(s) + H2O

NH4Cl(aq) + NaHCO3(s)

(Eq. 1)

A common side-reaction that occurs during the heating of the Bicarbonate to drive off Ammonium Chloride (NH4Cl) is the conversion of some of the Bicarbonate to Sodium Carbonate (Na2CO3): 2 NaHCO3(s)

Na2CO3(s) + CO2(g) + H2O(g)

(Eq. 2)

Thus, we wish to analyze our product to determine the percentage Sodium Bicarbonate and Sodium Carbonate it contains.

Sodium Bicarbonate

Sodium Carbonate

We will use a form of Volumetric Analysis called Titrimetry to analyze our product for these percentages. A volumetric analysis involves measuring the volume of a solution of known concentration, the Titrant, which is needed to completely react with an Analyte; Sodium Bicarbonate and Sodium Carbonate, in the present case. This titration reaction is complete when a stoichiometrically equivalent amount of titrant has been added to the analyte and all the analyte has been consumed. The point at which this occurs, called the Endpoint, is visually noted because an added Indicator changes color, or has some other distinct visual change, when the

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titration reaction is complete. The trick in any titration is to stop adding titrant at the exact point at which the indicator's color changes because only at this point will a stoichiometrically correct amount of titrant have been added to the analyte.

A Buret is the volume measuring device used to deliver the titrant into the analyte Solution.

A Graduated 50 mL Burette (http://en.wikipedia.org/wiki/File:Burette_vertical.svg)

This device is constructed such that it can be read with a high degree of precision. Accepted tolerances for burets are listed in the Appendix below. The amount (moles) of analyte present can be calculated from the volume of titrant added to reach the endopoint via: # moles Analyte = (Stoich. Ratio) x MTitrant x (Vf - Vi)

(Eq. 3)

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Here, (Stoich. Ratio) refers to the reaction stoichiometry between the Titrant and the Analyte in the titration reaction. Once the number of moles of Analyte has been determined, its mass can then be calculated using its molecular weight. In our case, we have two analytes in our sample; Sodium Bicarbonate and Sodium Carbonate. Both of these Sodium salts are water soluble and ionize upon solvation in Water: NaHCO3(aq)

Na+(aq) + HCO3-(aq)

(Eq. 4)

Na2CO3(aq)

2 Na+(aq) + CO32-(aq)

(Eq. 5)

The resulting Bicarbonate (HCO3-) and Carbonate (CO32-) ions are both basic. Hence, they will react with a strong acid such as Hydrochloric Acid (HCl), which itself ionizes to H+(aq) and Cl(aq) in Water. CO32-(aq) + H+(aq)

HCO3-(aq)

(Eq. 6)

HCO3-(aq) + H+(aq)

H2CO3(aq)

(Eq. 7)

Therefore, an acid such as HCl can serve as the titrant for our titration.

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Because we have two analytes, HCO3- and CO32-, we will need two different indicators, one to indicate the endpoint for the reaction between H+ and CO32- and the other to indicate the endpoint for the reaction between H+ and HCO3-. The indicator Phenolphthalein will serve as an endpoint indicator for the former reaction and Bromcresol Green will indicate the endpoint for the latter. We will add acid to a solution of our sample until the acid completely reacts with the Carbonate (CO32-) present to form Bicarbonate (HCO3-). The number moles Carbonate present can be determined from the Volume and Molarity of the acid added: # moles CO32- = (1 mole CO32-/1 mole H+) x MHCl x VHCl(1st EndPt)

(Eq. 8)

The Endpoint of this reaction can be detected because the Acid-Base Indicator Phenolphthalein will change color from Pink to Clear at the pH prevailing when this reaction is complete. After this endpoint is reached, the acid will begin reacting with the Bicarbonate just generated and the Bicarbonate present in the initial sample. And, again, knowing the Volume and Molarity of the added acid, we can determine the number moles Bicarbonate: # moles HCO3- Total = (1 mole HCO3-/1 mole H+) x MHCl x VHCl(1st to 2nd EndPt) (Eq. 9)

The Endpoint of this reaction can be detected by using the Acid-Base Indicator Bromocresol Green; which changes from Blue to Yellow at the pH that prevails at the completion of this reaction. The amount of Bicarbonate present in the original sample will then be the difference between the total Bicarbonate determined above and the amount generated by the Carbonate initially present. Thus, the amount of Bicarbonate originally present in our sample is given by: # mole HCO3- Original = # moles HCO3- Total - # moles CO32-

(Eq. 10)

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This entire procedure depends on knowing the concentration of the acid used as the titrant. We will determine this concentration using a Standardization procedure. This involves performing the same experiment on a sample of Sodium Carbonate of known mass. CO32-(aq) + 2 H+(aq)

H2CO3(aq)

(Eq. 11)

Then, # moles HCl = [mass Na2CO3 / MWNa2CO3] x (2 mole HCl/1 mole Na2CO3) (Eq. 12)

Molarity HCl = # moles HCl / VHCl[L]

(Eq. 13)

Finally, the Carbonic Acid produced as a result of these titrations can decompose into Carbon Dioxide (CO2): H2CO3(aq)

CO2(g) + H2O

(Eq. 14)

We can drive our titration reactions to completion by boiling the analyte solution to drive off any CO2 producded. So, we will first Standardize our HCl solution against a known mass of Sodium Carbonate. Then we will determine the percentage Sodium Carbonate in our sample by titrating it with the standardized acid to a Phenolphthalein endpoint. We will subsequently determine the percentage Sodium Bicarbonate by titrating the resulting solution to a Bromocresol Green endpoint.

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Pre-Lab Safety Questions 1.

When diluting a more concentrated acid solution, why is it advisable to add the acidic solution to Water, with stirring, rather than add the Water to the acidic solution?

2.

What should you do if a small amount of a dilute acid solution gets on your skin? What if the amount is much larger and the acid is more concentrated?

3.

If a dilute acid solution gets in your eyes, you should flush your eyes in the eye-wash. For how long should you flush them?

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Procedure Preparation of ~0.1M HCl Solution 1.

Use the 8M HCl provided to prepare 400 mL of ~0.1M HCl. Have your instructor check your Pre-Lab calculation before you proceed.

Standardization 1.

Set-up a buret to deliver your acid solution. Your instructor will demonstrate how to use this device. Do not proceed without this instruction.

2.

Fill your buret with the HCl solution. Your instructor will demonstrate this. Make sure the buret tip is full. Make an initial volume reading to the correct precision; 0.02 mL for a 50 mL buret.

3.

Weigh a sample of 0.20g Sodium Carbonate to a precision of 0.1mg on glazed weighing paper. Add this to a 250 mL Erlenmeyer Flask. Add about 25 mL Water and swirl to dissolve the Carbonate. Add a few drops of Phenolphthalein.

4.

Begin adding the acid to the flask from the buret no faster than 0.5 mL/second. Swirl the flask constantly. Continue until the pink color disappears. Now add 2-4 drops of Bromocresol Green (blue at high pH and yellow at low pH). Titrate to a blue-green color, which appears just before the Endpoint. Interrupt the titration at this point and boil the solution carefully for two or three minutes to drive off the Carbon Dioxide. This helps drive the reaction to completion. The color should revert to blue. Cool the solution to Room Temperature (~10 minutes) and continue the addition of acid to the pale green Endpoint. Make a volume reading at this point.

5.

Repeat this procedure twice more.

Analysis of Sample 1.

Weigh a sample of 0.20g Sample to a precision of 0.1mg on glazed weighing paper. Add this to a 250 mL Erlenmeyer Flask. Add about 25 mL Water and swirl to dissolve the Carbonate. Add a few drops of Phenolphthalein.

2.

Again fill your buret and make a volume reading.

3.

Add acid until you reach the Phenolphthalein Endpoint. Make a volume reading.

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4.

Add a few drops of Bromocresol Green and finish the addition of acid as before. Make a volume reading.

5.

Repeat the procedure at least twice more.

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Data Analysis 1.

Determine the Molarity of the HCl solution based on the data for each of the three Standardization experiments. Report the average value.

2.

Determine the number of moles Sodium Carbonate and Sodium Bicarbonate in each sample analyzed.

3.

Convert the number of moles of each substance to numbers of grams using the appropriate molecular weights.

4.

Calculate the Weight Percentage of Sodium Carbonate and Sodium Bicarbonate in each sample. Report the respective averages.

P a g e | 10

Post Lab Questions 1.

Suppose a titration of 0.200g of Sodium Carbonate requires 35.50 mL of HCl. What is the molarity of the HCl solution?

2.

Suppose the above titration (problem #1) is in error by 0.05 mL; too much. What is the percentage error introduced into the molarity of the HCl solution?

3.

The indicator Thymol Blue changes color (Blue to Yellow) over the same pH range as Phenolphthalein. Why is Phenolphthalein a better choice of indicator than Thymol Blue?

P a g e | 11

Appendix - Tolerances for Class A Volumetric Burets at 20oC

Capacity (mL) 5 10 25 50 100

Tolerances (mL) 0.01 0.02 0.03 0.05 0.20

With the exception of Graduated Cylinders, the Tolerances for Class B devices is typically twice that of a Class A device. (ASTM E694)

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