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CHEM1612 - Pharmacy Week 9: Concentration Cells

CHEM1612 - Pharmacy Week 9: Concentration Cells. Dr. Siegbert Schmid School of Chemistry, Rm 223 Phone: 9351 4196 E-mail: siegbert.schmid@sydney.edu.au. Unless otherwise stated, all images in this file have been reproduced from:

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CHEM1612 - Pharmacy Week 9: Concentration Cells

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  1. CHEM1612 - PharmacyWeek 9: Concentration Cells Dr. SiegbertSchmid School of Chemistry, Rm 223 Phone: 9351 4196 E-mail: siegbert.schmid@sydney.edu.au

  2. Unless otherwise stated, all images in this file have been reproduced from: Blackman, Bottle, Schmid, Mocerino and Wille,Chemistry, John Wiley & Sons Australia, Ltd. 2008      ISBN: 9 78047081 0866

  3. Electrochemistry • Blackman, Bottle, Schmid, Mocerino & Wille: Chapter 12, Sections 4.8 and 4.9 Key chemical concepts: • Redox and half reactions • Cell potential • Voltaic and electrolytic cells • Concentration cells Key Calculations: • Calculating cell potential • Calculating amount of product for given current • Using the Nernst equation for concentration cells

  4. Silver electrode Ag+ + e– Ag AgCl Ag+ + Cl– Overall: AgCl + e– Ag + Cl– E0 = 0.22 V AgCl (s) + e–Ag (s) + Cl– (sat) A thin coating of AgCl is deposited on the pure metal surface. Ag|AgCl|Cl–

  5. ? 0.22 Ag+/Ag 0.0V H2/H+ Pop Quiz 2 • A Fe3+/Fe2+ cellwith [Fe3+]=[Fe2+] =1 M has a potential of 0.55V respect to the Ag/AgCl electrode (E0= 0.22 V). What is the potential of this electrode respect to the SHE? Answer. The reaction that occurs in the two half-cells are: Fe3+ + e- → Fe2+ at the cathode E = 0.55 V; E0 = ? Ag + Cl- +e-→ AgCl at the anode E0= 0.22 V The potential of this electrode respect to the SHE is the difference of the two electrode potentials: E = E0 - 0.22 E0Fe3+/Fe2+ = 0.55 + 0.22 = 0.77 V

  6. Measurement of pH We could construct a concentration cell, using the standard hydrogen electrode (SHE) and a hydrogen electrode: H2(g, 1 atm) 2H+(aq, unknown) + 2e-anode 2H+ (aq, 1M) + 2e-H2(g, 1 atm) cathode 2H+ (1M) 2H+ (unknown) Ecell = ? unknown

  7. pH electrode The pH electrode potential is typically measured versus a fixed reference calomel electrode. E’ is the sum of the constant offset potentials of the inner glass surface/solution, the Ag/AgCl electrode, and the calomel electrode. Eglass electrode= E’ + RT/2.303F log [H+] • Based on a thin glass membrane: a modified glass enriched in H+ and resulting in a hydration layer a few micrometers thick. • Inside the membrane is a 'reference solution' of known [H+] (1M HCl). • The potential difference relevant to pH measurement builds up across the outside glass/solution interface marked ||.

  8. Nernst Equation The Nernst equation describes the effect of concentration on cell potential. Zn(s) + Cu2+(aq) Zn2+(aq) + Cu(s) When Q < 1, [reactants] >[products] and the cell can do more work. When Q = 1, Ecell = E0cell (standard conditions [x] = 1 M). When Q > 1 , [products] > [reactants] and Ecell is lower.

  9. - K 0 V ~1037 Ecell decreases as the reaction proceeds, until at equilibrium Ecell= 0 and . Potential of an electrochemical cell Zn(s) + Cu2+(aq) Zn2+(aq) + Cu(s) Ecell (Volts)

  10. Recap: Examining Q To K Ratios If Q/K < 1 • Ecell is positive for the reaction as written. The smaller the Q/K ratio, the greater the value of Ecell and the more electrical work the cell can do. If Q/K = 1, • Ecell = 0. The cell is at equilibrium and can no longer do work. If Q/K > 1, • Ecell is negative for the reaction as written. The cell will operate in reverse – the reverse reaction will take place and do work until Q/K = 1 at equilibrium.

  11. At equilibrium Q=K Link between E 0 and K Q: What happens if the reaction proceeds until equilibrium is reached? A: The reaction stops, therefore the voltage, or electrical potential, is zero (the battery is flat). In mathematical terms: So the equilibrium constant determines the cell potential. Large K products favoured  large standard cell potential, E0

  12. Redox reactions are special • For redox reactions there is a direct experimental method to measure K and ΔG°.

  13. Relation between E 0 and K Figure from Silberberg, “Chemistry”, McGraw Hill, 2006. K is plotted on a logarithmic scale to give a straight line.

  14. Example question 2 Q: A voltaic cell consisting of a Ni/Ni2+ half-cell and Co/Co2+ half-cell is constructed with the following initial concentrations: [Ni2+] = 0.80 M; [Co2+]=0.2 M. a) What is the initial Ecell? b) What is the [Ni2+] when the voltage reaches 0.025 V? c) What are the equilibrium concentrations of the ions? Given: E 0Ni2+/Ni = -0.25 V; E 0Co2+/Co = -0.28 V Ni2+ + 2e- →NiE 0 = -0.25V Co →Co2+ + 2e- E 0 = +0.28V Co(s) + Ni2+(aq)  Co2+(aq) + Ni(s) E 0 = 0.03 V

  15. Example question 2a a) What is the initial Ecell? Co(s) + Ni2+(aq)  Co2+(aq) + Ni(s) E 0 = 0.03 V

  16. Example question 2b b) What is the [Ni2+] when the voltage reaches 0.025V? Q = 1.47 Co(s) + Ni2+(aq)  Co2+(aq) + Ni(s)

  17. Co(s) + Ni2+(aq)  Co2+(aq) + Ni(s) 0.80-x 0.20+x Example question 2c c) What are the equilibrium concentrations of the ions? K = 10.24

  18. Concentration Cells in Nature Concentration cells are present all around us, e.g. • nerve signalling: concentration gradients produce electrical current • ion pumps across cell membranes: Na+ / K+ pump, Ca2+ pump • energy production and storage in cells: ATP

  19. Nerve cells Energy from ATP hydrolysis is used by ion pumps, so that across the nerve cell membrane concentration gradients are maintained: Ion Concentration Gradient: Inside Outside K+High Low Na+Low High The membrane potential is more positive outside than inside the cell. • On nerve stimulation, Na+ enters cell, the inside cell membrane becomes > +ive, then K+ ions leave cell to re-equilibrate the outside. • These rapid (ms) changes in charge across the membrane stimulate the neighbouring region and the electrical impulse moves down the length of the cell. Figure from Silberberg, “Chemistry”, McGraw Hill, 2006.

  20. Nerve cells • Nernst Equation gives the membrane potential generated by the differing extracellular versus intracellular concentrations of each ion: Substituting n = 1, T = 37oC: ( in mV) 1 mV = 10-3 V

  21. Cellular Electrochemistry • Biological cells apply the principles of electrochemical cells to generate energy in a complex multistep process. • Bond energy in food is used to generate an electrochemical potential. • The potential is used to create the bond energy of the high-energy molecule adenosine triphosphate (ATP) (energy currency for the cell). ATP4- + H2O→ADP3- + HPO42- + H+ ΔG °’ = -30.5 kJ mol-1 ΔGo’ (solution at pH 7 and at human body temperature 37oC.)

  22. Inside mitochondria, redox reactions are performed by a series of proteins that form the electron-transport chain (ETC) which contain redox couples, such as Fe2+/Fe3+. Large potential differences provide enough energy to convert ADP into ATP. Bond Energy to Electrochemical Potential Figure from Silberberg, “Chemistry”, McGraw Hill, 2006.

  23. Bond Energy to Electrochemical Potential In nature, the most important reducing agent is a complex molecule named nicotinamide adenine dinucleotide, abbreviated NADH, which functions as a hydride donor (H-). = NADH = biological reducing agent NAD+ = biological oxidising agent

  24. Electron Transport Chain (ETC) ETC consists of three main steps, each of which has a high enough potential difference to produce one ATP molecule. The reaction that ultimately powers ETC is the reduction of oxygen in the presence of NADH: 2H+ + 2e- + ½ O2→H2O Eo’ = +0.82 NADH + H+→NAD+ + 2H+ + 2e-Eo’ = -0.32 NADH(aq) + H+(aq) + ½O2(aq)→NAD+(aq) + H2O(l) Eo’overall = 1.14 V Substantial energy release! ΔGo’ = -nFEo’ = -2 · 96485 C mol-1· 1.14 V = - 220 kJ mol-1

  25. ATP Synthesis • In short: e- are transported along the chain, while protons are forced into the intermembrane space. • This creates a H+concentration cell across the membrane. • In this step, the cell acts as an electrolytic cell, i.e. uses a spontaneous process to drive a non-spontaneous process. • When [H+]intermembrane/[H+]matrix ~ 2.5 a trigger allows protons to flow back across membrane, and ATP is formed. Figure from Silberberg, “Chemistry”, McGraw Hill, 2006. • It’s not simple: Noble prize in 1997 to Boyer and Walker for elucidating this.

  26. Summary CONCEPTS • Concentration cells • Nernst equation • E 0 and K • Link between E , Q and K • Applications of concentration cells CALCULATIONS • Work out cell potential from reduction potentials; • Work out cell potential for any concentration (Nernst equation) • Work out K from E 0 • Work out pH from concentration cell

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