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Experiment 7
Objective
 Apply the concept of complexometric titration in the
 determination of total hardness in drinking water
Simple Water and Complexes
Water
 Drinking
   Hard water is better for
    drinking because it
    contains minerals
Water
         Cleaning
           Soft water is better for
            cleaning because it
            doesn’t form scum with
            soap
Water
 Hardness of water
   Depends on source
   Caused by Ca2+ and
    Mg2+ forming
    precipitates with soap
Water
         Hardness of water
           Most Ca2+ in water
            come from CaCO3
            exoskeletons of aquatic
            microorganisms like
            diatoms
Complexes
 Coordination between
  metal and ligand
    An atom in the ligand
     (called the donor)
     donates electrons to the
     metal ion, forming a
     bond.
 New properties
    Complexes are usually
     more stable than the
     components due to the
     rearrangement of the
     energy levels of the d-
     orbital (crystal field
     theory)
Complexes - Ligands
                Monodentate
                Polydentate
                   Chelating agents – Gr.
                    “chelos”, meaning teeth
                      Polyanionic
                      Complex-forming
                      Reacts in a 1:1 ratio
Complexes - Usage
 Catalysts
   Polymerization, hydrogenation, hydroboration, etc.
 Medicine
   cis-diamminedichloroplatinum(II)
                                        Cl            NH3
 Chelators
   Heavy Metal Poisoning Treatment
                                               Pt
   Cleaning agent
   Food enhancement
                                        Cl            NH3
   Anti-b acterial
   Titrants
Step by step discussion
*simple dilutions are not discussed
Solution Preparation
Solution Preparation
 250 mL 0.050 M std CaCO3soln
                           + 20 mL dH2O, +few             Cover with watch
                           drops 6M HCl                   glass (slower
     1.2511 g CaCO3
                           (Dissolve                      evaporation rate to
     standard
                           precipitate, basic             keep beaker from
                           CO32-)                         getting dry)
            Rinse watch glass to                  Evaporate to 10 mL.
            beaker                                Cool.


 Quantitatively transfer to 250 mL vol flask. Dilute to mark.
Solution Preparation
 pH 10 buffer
                                                Transfer to 250 mL
  142 mL conc NH3 +
                        Adjust soln to pH 10    vol flask. Dilute to
  17.5 g NH4Cl
                                                mark.



     pOH     pKb log([NH 4 ] /[ NH 3 ])
     pOH       log(1.8 x10 5 ) log(2.1016m ol/ 0.327m ol)
     pOH     4.74 0.808
      pH     8.45
Add ammonia to increase pH!
Solution Preparation
 pH 10 buffer
                                             Transfer to 250 mL
  142 mL conc NH3 +
                      Adjust soln to pH 10   vol flask. Dilute to
  17.5 g NH4Cl
                                             mark.


 Different minimum pH values for different cations
   Mn2+, Fe2+,  5-6 pH
   Fe3+, Th4+  1-1.5 pH
   Ca2+  8
   Mg2+  10
Solution Preparation
 pH 10 buffer
                                           Transfer to 250 mL
142 mL conc NH3 +
                    Adjust soln to pH 10   vol flask. Dilute to
17.5 g NH4Cl
                                           mark.


 As a rule of thumb,
    The higher the pH (more basic solution), the sharper
     the endpoint
    The higher the formation of constant the lower the
     minimum pH
Solution Preparation
 500 mL 0.050 M EDTA

                                          +1.0 g
9.31 g Na2H2EDTA•2H2O   +200 mL dH2O
                                          MgCl2•6H2O


                                       Dissolve in 500 mL vol
                                       flask. Heat if
                                       necessary.
Solution Preparation
 500 mL 0.050 M EDTA
 Why add 1.0 g MgCl2•6H2O?
   Diverse ion effect: increase solubility (easier
    preparation)
   Sharper endpoint in titration
        Ensures presence of Mg2+ in sample
        Supposedly does not affect titration procedure
 What exactly happens when we add MgCl2?
   Good question.
Solution Preparation
 500 mL 0.050 M EDTA
 What happens when we DON’T add MgCl2?
   Endpoint not as sharp if Mg2+ is not present in solution
   Only total hardness can be computed (Ca2+ and Mg2+)
                      HO       O
                           S
                      O
                                       O
                                               O
              O                        Mg
                  N                N
                                           N
               O

       Figure 1. Structure of eriochrome black T – magnesium complex
Standardization




           http://xkcd.com/927/
Standardization
 10.00m L 0.0050 M wrk    + 3 mL buffer       Titrate to blue
 std CaCO3                + 6 drps EBT        endpoint


 Reactions: (Consider w/o MgCl2)
   Start:
       Ca2+ + HIn2-  CaHIn (Kf = 2.5x105)
   Before equivalence point:
       Ca2+ + H2Y2-  CaH2Y(Kf = 5.0x1010)
   At the end point:
       CaHIn + Y2-  CaH2Y + HIn2-
Standardization
     w/o MgCl2


Ca2+ + HIn2- 
CaHIn




           Ca2+ + H2Y2-  CaH2Y
                                  CaHIn + Y2-  CaH2Y + HIn2-
Standardization
 10.00 mL 0.0050 M wrk        + 3 mL buffer        Titrate to blue
 std CaCO3                    + 6 drps EBT         endpoint

 Reactions: (Consider w/ MgCl2)
    Start:
        Ca2+ + HIn2-  CaHIn (Kf = 2.5x105)    Calcium-EBT complexation
   Before equivalence point:
        Ca2+ + H2Y2-  CaH2Y(Kf = 5.0x1010)        Calcium consumption
        Ca2+ + MgH2Y  CaH2Y + Mg2+             Magnesium Displacement
        Mg2+ + CaHIn  MgHIn + Ca2+         Magnesium-EBT complexation
   Near the endpoint: Assume all Ca2+ consumed
        Mg2+ + H2Y2-  MgH2Y             Released Magnesium consumption
   At the end point:
        MgHIn + H2Y2-  MgH2Y + HIn2-           Magnesium Displacement
Standardization
     w/ MgCl2


Ca2+ + HIn2-                            Mg2+ + H2Y2-  MgH2Y
CaHIn




           Ca2+ + H2Y2-  CaH2Y
           Ca2+ + MgH2Y  CaH2Y + Mg2+         MgHIn + H2Y2-  MgH2Y + HIn2-
           Mg2+ + CaHIn  MgHIn + Ca2+
Standardization
 w/ MgCl2

                                Amount of EDTA corresponding to
                                Free EDTA to titrate released Mg2+




             Amount of EDTA to titrate Ca2+      Amount of EDTA to
                                                 titrate Mg2+ in
                                                 indicator (negligible)
Standardization
 The amount of MgCl2 that was supposed to be
 added was not in significant (0.0049 mol, compared
 to EDTA that has 0.025 mol)

 The addition of MgCl2 should be stoichiometric (Y=X)
 or negligible (Y≈0) to EDTA in order for the titration to
 be unaffected
Sample Analysis
Sample Analysis
             50 mL         + 3 mL buffer       Titrate to blue
             Viva          + 6 drps EBT        endpoint

 Reactions: (Consider w/o MgCl2)
    Start:
       Mg2+ + HIn2-  MgHIn (Kf = 1.0x107) Magnesium-EBT complexation
   Before equivalence point:
       Ca2+ + H2Y2-  CaH2Y(Kf = 5.0x1010)       Calcium consumption
   Near the endpoint: Assume all Ca2+ consumed
       Mg2++H2Y2-MgH2Y(Kf=4.9x108) Present Magnesium consumption
   At the end point:
       MgHIn + H2Y2-  MgH2Y + HIn2-         Magnesium Displacement
Sample Analysis
     w/o MgCl2

                                 Mg2+ + H2Y2-  MgH2Y
Mg2+ + HIn2-  MgHIn




          Ca2+ + H2Y2-  CaH2Y
                                    CaHIn + Y2-  CaH2Y + HIn2-
Sample Analysis
             50 mL        + 3 mL buffer        Titrate to blue
             Viva         + 6 drps EBT         endpoint

 Reactions: (Consider w/ MgCl2)
    Start:
       Mg2+ + HIn2-  MgHIn (Kf = 1.0x107) Magnesium-EBT complexation
   Before equivalence point:
     Ca2+ + H2Y2-  CaH2Y(Kf = 5.0x1010)        Calcium consumption
      Ca2+ + MgH2Y  CaH2Y + Mg2+                  Magnesium release
   Near the endpoint: Assume all Ca2+ consumed
     Mg2++H2Y2-MgH2Y(Kf=4.9x108) Present Magnesium consumption
                                  Released Magnesium consumption
   At the end point:
     MgHIn + H2Y2-  MgH2Y + HIn2-          Magnesium Displacement
Sample Analysis
     w/ MgCl2


Mg2+ + HIn2-  MgHIn                    Mg2+ + H2Y2-  MgH2Y




          Ca2+ + H2Y2-  CaH2Y
          Ca2+ + MgH2Y  CaH2Y + Mg2+         MgHIn + H2Y2-  MgH2Y + HIn2-
Sample Analysis
 w/ MgCl2

                             Amount of EDTA corresponding to
                             Free EDTA to titrate released and present Mg2+




             Amount of EDTA to titrate Ca2+      Amount of EDTA to
                                                 titrate Mg2+ in
                                                 indicator (negligible)
Sample Analysis
 w/ MgCl2

                  Y




             X    Amount of EDTA to
                  titrate Mg2+ in
                  indicator (negligible)
Sample Analysis
 w/ MgCl2
    Let X =

    Y=
                 Y




              X
Sample Analysis
 w/ MgCl2
    Let X =

    Y=
                 Y




              X
Sample Analysis
 The amount of MgCl2 that was supposed to be
  added was significant (0.0049 mol, compared to
  EDTA that has 0.025 mol)
 The addition of MgCl2 should be negligible
  (EDTA:Mg≈0) with respect to EDTA in order for the
  titration to be unaffected
Sample Analysis
 Back Titration with EDTA is possible
    Add standardized amount of EDTA
    Back titrate with Mg2+
Molarity of Primary Standard
 Weight 1o std: 1.2511 g
 %Purity 1o std: 99.9%
 Final volume std: 250 mL
 Vol std sol'n: 5 mL
 Final vol working std: 50 mL
Molarity of Primary Standard
 The molarity of the working standard can be
 computed from the given
Volume of titrant used in
standardization
               Trial 1   Trial 2   Trial 3
   Volume
working std      10        10        10
   CaCO3
Final volume    14.1       28       41.8
    Initial
                0.4       14.1       28
   volume
 Net volume     13.7      13.9      13.8
Molarity of EDTA
       Volume    Net volume
                              Molarity
      wrking std   EDTA
Std A   10 mL     13.7 mL

 Molarity:
Titer of EDTA
                 nEDTA =
       Molarity            Titer
                 nCaCO3
Std A 0.003646 M    1

 Titer:
Total Hardness of Viva
         Volume of              Total
                                          Total hardness in ppm
          Water    Vol EDTA   Amount of
                                                 CaCO3
          Sample               Calcium
Sample A  50 mL     19.5 mL

 Total Amount of Calcium:



 Total hardness in ppm CaCO3:
Collective Data
  Team      Group   Trial1   Trial2   Trial3   Average
              1     142.58   142.58   139.02    141.40
    1         2
              3     140.61   139.89   140.61   140.37
Team Mean                                      140.88
              4     148.57   149.32   147.83   148.57
    2         5     151.40   140.83   140.13   144.12
              6     141.29   142.02   144.92   142.74
Team Mean                                      145.14
             7      148.38   138.63   136.54   141.19
             8
    3
             9
             10     139.15   142.66   138.45   140.09
Team Mean                                      140.64

  Mean                                         142.64
  Stdev                                         4.73
  RSD                                           33.2
To Viva or not to Viva, that is the question
PPM Viva
 Total hardness of 192.49 ppm CaCO3
Conclusion
 25.8% difference between the mean and the claimed
  value

 Viva’s water is softer than they claim it to be
References
   J. Roger Hart; J. Chem. Educ., 1984, 61 (12), p 1060.
   Blitz, Jonathan P. COMPLEXOMETRIC DETERMINATION OF Mg2+ and Ca2+. 2010. 25 January
    2012 <http://www.ux1.eiu.edu/~cfjpb/teaching/quant/labs/experiment8.pdf>.
   Garrett, Simon J. CEM 333 EDTA Formation Constants. 1998. 25 January 2012
    <http://www.cem.msu.edu/~cem333/EDTATable.html>.
   Jackson School of Geosciences. COORDINATION CHEMISTRY. n.d. 25 January 2012
    <http://www.geo.utexas.edu/courses/376m/coord_chem.htm>.
   Jon A. McCleverty, Thomas J. Meyer. "Applications of Coordination Complexes." 2003. Platinum
    Metals Review. 25 January 2012 <http://www.platinummetalsreview.com/pdf/101-104-pmr-
    jul04.pdf>.
   Mccord, Dr. Stephen P. Determination of Water Hardness using Complexometric titration. 2005. 25
    January 2012 <http://mccord.cm.utexas.edu/courses/spring2005/ch455/Spr05455Wk4Lab.pdf>.
   Old Dominion University. Chapter 12: EDTA Titrations. n.d. 25 January 2012
    <http://www.odu.edu/sci/xu/chem321/chem321chapter12.pdf>.
   Prince George's Community College. ANALYSIS OF CALCIUM BY EDTA TITRATION TO ASSESS
    WATER . n.d. 25 January 2012 <http://academic.pgcc.edu/psc/chm103/EDTA_Ca.pdf>.
   Reckhow Research Group. CHAPTER XVI VOLUMETRIC METHODS. 17 June 2011. 25 January
    2012 <http://www.ecs.umass.edu/cee/reckhow/courses/572/572bk16/572BK16.html>.
   Sinex, Scott A. EDTA - A Molecule with a Complex Story. 1 August 2007. 25 January 2012
    <http://www.chm.bris.ac.uk/motm/edta/edtah.htm>.
   UC Davis Department of Chemistry. EDTA TITRATIONS. 31 March 2004. 25 January 2012
    <http://www-chem.ucdavis.edu/2C/Old/06EDTA.pdf >.
“He who asks is a fool for five minutes, but he who
            does not ask remains a fool forever.”

                                       Chinese Proverb

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Quantitative Determination of Total Hardness in Drinking Water by Complexometric EDTA Titration

  • 2. Objective  Apply the concept of complexometric titration in the determination of total hardness in drinking water
  • 3. Simple Water and Complexes
  • 4. Water  Drinking  Hard water is better for drinking because it contains minerals
  • 5. Water  Cleaning  Soft water is better for cleaning because it doesn’t form scum with soap
  • 6. Water  Hardness of water  Depends on source  Caused by Ca2+ and Mg2+ forming precipitates with soap
  • 7. Water  Hardness of water  Most Ca2+ in water come from CaCO3 exoskeletons of aquatic microorganisms like diatoms
  • 8. Complexes  Coordination between metal and ligand  An atom in the ligand (called the donor) donates electrons to the metal ion, forming a bond.  New properties  Complexes are usually more stable than the components due to the rearrangement of the energy levels of the d- orbital (crystal field theory)
  • 9. Complexes - Ligands  Monodentate  Polydentate  Chelating agents – Gr. “chelos”, meaning teeth  Polyanionic  Complex-forming  Reacts in a 1:1 ratio
  • 10. Complexes - Usage  Catalysts  Polymerization, hydrogenation, hydroboration, etc.  Medicine  cis-diamminedichloroplatinum(II) Cl NH3  Chelators  Heavy Metal Poisoning Treatment Pt  Cleaning agent  Food enhancement Cl NH3  Anti-b acterial  Titrants
  • 11. Step by step discussion *simple dilutions are not discussed
  • 13. Solution Preparation  250 mL 0.050 M std CaCO3soln + 20 mL dH2O, +few Cover with watch drops 6M HCl glass (slower 1.2511 g CaCO3 (Dissolve evaporation rate to standard precipitate, basic keep beaker from CO32-) getting dry) Rinse watch glass to Evaporate to 10 mL. beaker Cool. Quantitatively transfer to 250 mL vol flask. Dilute to mark.
  • 14. Solution Preparation  pH 10 buffer Transfer to 250 mL 142 mL conc NH3 + Adjust soln to pH 10 vol flask. Dilute to 17.5 g NH4Cl mark. pOH pKb log([NH 4 ] /[ NH 3 ]) pOH log(1.8 x10 5 ) log(2.1016m ol/ 0.327m ol) pOH 4.74 0.808 pH 8.45 Add ammonia to increase pH!
  • 15. Solution Preparation  pH 10 buffer Transfer to 250 mL 142 mL conc NH3 + Adjust soln to pH 10 vol flask. Dilute to 17.5 g NH4Cl mark.  Different minimum pH values for different cations  Mn2+, Fe2+,  5-6 pH  Fe3+, Th4+  1-1.5 pH  Ca2+  8  Mg2+  10
  • 16. Solution Preparation  pH 10 buffer Transfer to 250 mL 142 mL conc NH3 + Adjust soln to pH 10 vol flask. Dilute to 17.5 g NH4Cl mark.  As a rule of thumb,  The higher the pH (more basic solution), the sharper the endpoint  The higher the formation of constant the lower the minimum pH
  • 17. Solution Preparation  500 mL 0.050 M EDTA +1.0 g 9.31 g Na2H2EDTA•2H2O +200 mL dH2O MgCl2•6H2O Dissolve in 500 mL vol flask. Heat if necessary.
  • 18. Solution Preparation  500 mL 0.050 M EDTA  Why add 1.0 g MgCl2•6H2O?  Diverse ion effect: increase solubility (easier preparation)  Sharper endpoint in titration  Ensures presence of Mg2+ in sample  Supposedly does not affect titration procedure  What exactly happens when we add MgCl2?  Good question.
  • 19. Solution Preparation  500 mL 0.050 M EDTA  What happens when we DON’T add MgCl2?  Endpoint not as sharp if Mg2+ is not present in solution  Only total hardness can be computed (Ca2+ and Mg2+) HO O S O O O O Mg N N N O Figure 1. Structure of eriochrome black T – magnesium complex
  • 20. Standardization http://xkcd.com/927/
  • 21. Standardization 10.00m L 0.0050 M wrk + 3 mL buffer Titrate to blue std CaCO3 + 6 drps EBT endpoint  Reactions: (Consider w/o MgCl2)  Start:  Ca2+ + HIn2-  CaHIn (Kf = 2.5x105)  Before equivalence point:  Ca2+ + H2Y2-  CaH2Y(Kf = 5.0x1010)  At the end point:  CaHIn + Y2-  CaH2Y + HIn2-
  • 22. Standardization  w/o MgCl2 Ca2+ + HIn2-  CaHIn Ca2+ + H2Y2-  CaH2Y CaHIn + Y2-  CaH2Y + HIn2-
  • 23. Standardization 10.00 mL 0.0050 M wrk + 3 mL buffer Titrate to blue std CaCO3 + 6 drps EBT endpoint  Reactions: (Consider w/ MgCl2)  Start:  Ca2+ + HIn2-  CaHIn (Kf = 2.5x105) Calcium-EBT complexation  Before equivalence point:  Ca2+ + H2Y2-  CaH2Y(Kf = 5.0x1010) Calcium consumption  Ca2+ + MgH2Y  CaH2Y + Mg2+ Magnesium Displacement  Mg2+ + CaHIn  MgHIn + Ca2+ Magnesium-EBT complexation  Near the endpoint: Assume all Ca2+ consumed  Mg2+ + H2Y2-  MgH2Y Released Magnesium consumption  At the end point:  MgHIn + H2Y2-  MgH2Y + HIn2- Magnesium Displacement
  • 24. Standardization  w/ MgCl2 Ca2+ + HIn2-  Mg2+ + H2Y2-  MgH2Y CaHIn Ca2+ + H2Y2-  CaH2Y Ca2+ + MgH2Y  CaH2Y + Mg2+ MgHIn + H2Y2-  MgH2Y + HIn2- Mg2+ + CaHIn  MgHIn + Ca2+
  • 25. Standardization  w/ MgCl2 Amount of EDTA corresponding to Free EDTA to titrate released Mg2+ Amount of EDTA to titrate Ca2+ Amount of EDTA to titrate Mg2+ in indicator (negligible)
  • 26. Standardization  The amount of MgCl2 that was supposed to be added was not in significant (0.0049 mol, compared to EDTA that has 0.025 mol)  The addition of MgCl2 should be stoichiometric (Y=X) or negligible (Y≈0) to EDTA in order for the titration to be unaffected
  • 28. Sample Analysis 50 mL + 3 mL buffer Titrate to blue Viva + 6 drps EBT endpoint  Reactions: (Consider w/o MgCl2)  Start:  Mg2+ + HIn2-  MgHIn (Kf = 1.0x107) Magnesium-EBT complexation  Before equivalence point:  Ca2+ + H2Y2-  CaH2Y(Kf = 5.0x1010) Calcium consumption  Near the endpoint: Assume all Ca2+ consumed  Mg2++H2Y2-MgH2Y(Kf=4.9x108) Present Magnesium consumption  At the end point:  MgHIn + H2Y2-  MgH2Y + HIn2- Magnesium Displacement
  • 29. Sample Analysis  w/o MgCl2 Mg2+ + H2Y2-  MgH2Y Mg2+ + HIn2-  MgHIn Ca2+ + H2Y2-  CaH2Y CaHIn + Y2-  CaH2Y + HIn2-
  • 30. Sample Analysis 50 mL + 3 mL buffer Titrate to blue Viva + 6 drps EBT endpoint  Reactions: (Consider w/ MgCl2)  Start:  Mg2+ + HIn2-  MgHIn (Kf = 1.0x107) Magnesium-EBT complexation  Before equivalence point:  Ca2+ + H2Y2-  CaH2Y(Kf = 5.0x1010) Calcium consumption Ca2+ + MgH2Y  CaH2Y + Mg2+ Magnesium release  Near the endpoint: Assume all Ca2+ consumed  Mg2++H2Y2-MgH2Y(Kf=4.9x108) Present Magnesium consumption Released Magnesium consumption  At the end point:  MgHIn + H2Y2-  MgH2Y + HIn2- Magnesium Displacement
  • 31. Sample Analysis  w/ MgCl2 Mg2+ + HIn2-  MgHIn Mg2+ + H2Y2-  MgH2Y Ca2+ + H2Y2-  CaH2Y Ca2+ + MgH2Y  CaH2Y + Mg2+ MgHIn + H2Y2-  MgH2Y + HIn2-
  • 32. Sample Analysis  w/ MgCl2 Amount of EDTA corresponding to Free EDTA to titrate released and present Mg2+ Amount of EDTA to titrate Ca2+ Amount of EDTA to titrate Mg2+ in indicator (negligible)
  • 33. Sample Analysis  w/ MgCl2 Y X Amount of EDTA to titrate Mg2+ in indicator (negligible)
  • 34. Sample Analysis  w/ MgCl2 Let X = Y=  Y X
  • 35. Sample Analysis  w/ MgCl2 Let X = Y=  Y X
  • 36. Sample Analysis  The amount of MgCl2 that was supposed to be added was significant (0.0049 mol, compared to EDTA that has 0.025 mol)  The addition of MgCl2 should be negligible (EDTA:Mg≈0) with respect to EDTA in order for the titration to be unaffected
  • 37. Sample Analysis  Back Titration with EDTA is possible  Add standardized amount of EDTA  Back titrate with Mg2+
  • 38.
  • 39. Molarity of Primary Standard  Weight 1o std: 1.2511 g  %Purity 1o std: 99.9%  Final volume std: 250 mL  Vol std sol'n: 5 mL  Final vol working std: 50 mL
  • 40. Molarity of Primary Standard  The molarity of the working standard can be computed from the given
  • 41. Volume of titrant used in standardization Trial 1 Trial 2 Trial 3 Volume working std 10 10 10 CaCO3 Final volume 14.1 28 41.8 Initial 0.4 14.1 28 volume Net volume 13.7 13.9 13.8
  • 42. Molarity of EDTA Volume Net volume Molarity wrking std EDTA Std A 10 mL 13.7 mL  Molarity:
  • 43. Titer of EDTA nEDTA = Molarity Titer nCaCO3 Std A 0.003646 M 1  Titer:
  • 44. Total Hardness of Viva Volume of Total Total hardness in ppm Water Vol EDTA Amount of CaCO3 Sample Calcium Sample A 50 mL 19.5 mL  Total Amount of Calcium:  Total hardness in ppm CaCO3:
  • 45. Collective Data Team Group Trial1 Trial2 Trial3 Average 1 142.58 142.58 139.02 141.40 1 2 3 140.61 139.89 140.61 140.37 Team Mean 140.88 4 148.57 149.32 147.83 148.57 2 5 151.40 140.83 140.13 144.12 6 141.29 142.02 144.92 142.74 Team Mean 145.14 7 148.38 138.63 136.54 141.19 8 3 9 10 139.15 142.66 138.45 140.09 Team Mean 140.64 Mean 142.64 Stdev 4.73 RSD 33.2
  • 46. To Viva or not to Viva, that is the question
  • 47. PPM Viva  Total hardness of 192.49 ppm CaCO3
  • 48. Conclusion  25.8% difference between the mean and the claimed value  Viva’s water is softer than they claim it to be
  • 49. References  J. Roger Hart; J. Chem. Educ., 1984, 61 (12), p 1060.  Blitz, Jonathan P. COMPLEXOMETRIC DETERMINATION OF Mg2+ and Ca2+. 2010. 25 January 2012 <http://www.ux1.eiu.edu/~cfjpb/teaching/quant/labs/experiment8.pdf>.  Garrett, Simon J. CEM 333 EDTA Formation Constants. 1998. 25 January 2012 <http://www.cem.msu.edu/~cem333/EDTATable.html>.  Jackson School of Geosciences. COORDINATION CHEMISTRY. n.d. 25 January 2012 <http://www.geo.utexas.edu/courses/376m/coord_chem.htm>.  Jon A. McCleverty, Thomas J. Meyer. "Applications of Coordination Complexes." 2003. Platinum Metals Review. 25 January 2012 <http://www.platinummetalsreview.com/pdf/101-104-pmr- jul04.pdf>.  Mccord, Dr. Stephen P. Determination of Water Hardness using Complexometric titration. 2005. 25 January 2012 <http://mccord.cm.utexas.edu/courses/spring2005/ch455/Spr05455Wk4Lab.pdf>.  Old Dominion University. Chapter 12: EDTA Titrations. n.d. 25 January 2012 <http://www.odu.edu/sci/xu/chem321/chem321chapter12.pdf>.  Prince George's Community College. ANALYSIS OF CALCIUM BY EDTA TITRATION TO ASSESS WATER . n.d. 25 January 2012 <http://academic.pgcc.edu/psc/chm103/EDTA_Ca.pdf>.  Reckhow Research Group. CHAPTER XVI VOLUMETRIC METHODS. 17 June 2011. 25 January 2012 <http://www.ecs.umass.edu/cee/reckhow/courses/572/572bk16/572BK16.html>.  Sinex, Scott A. EDTA - A Molecule with a Complex Story. 1 August 2007. 25 January 2012 <http://www.chm.bris.ac.uk/motm/edta/edtah.htm>.  UC Davis Department of Chemistry. EDTA TITRATIONS. 31 March 2004. 25 January 2012 <http://www-chem.ucdavis.edu/2C/Old/06EDTA.pdf >.
  • 50. “He who asks is a fool for five minutes, but he who does not ask remains a fool forever.” Chinese Proverb