160 likes | 727 Views
Accuracy of the Debye-H ü ckel limiting law. Example : The mean activity coefficient in a 0.100 mol kg -1 MnCl 2 (aq) solution is 0.47 at 25 o C. What is the percentage error in the value predicted by the Debye-Huckel limiting law?
E N D
Accuracy of the Debye-Hückel limiting law Example: The mean activity coefficient in a 0.100 mol kg-1 MnCl2(aq) solution is 0.47 at 25oC. What is the percentage error in the value predicted by the Debye-Huckel limiting law? Solution: First use equation 10.4 to calculate the ionic strength and then use eq. 10.3 to calculate the mean activity coefficient. From eq. 10.4, I = ½(22*0.1 + 12*(2*0.1)) = 0.3 From eq. 10.3 log(γ) = -|2*1|A*(0.3)1/2; = - 2*0.509*0.5477 = - 0.5576 so γ = 0.277 Error = (0.47-0.277)/0.47 * 100% = 41%
Extended Debye-Hückel law • (10.5) B is an adjustable empirical parameter.
Calculating parameter B Example : The mean activity coefficient of NaCl in a diluted aqueous solution at 25oC is 0.907 (at 10.0mmol kg-1). Estimate the value of B in the extended Debye-Huckel law. Solution: First calculate the ionic strength I = ½(12*0.01 + 12*0.01) = 0.01 From equation 10.5 log(0.907) = - (0.509|1*1|*0.011/2)/(1+ B*0.011/2) B = - 1.67
Half-reactions and electrodes Two types of electrochemical cells: 1. Galvanic cell: is an electrochemical cell which produces electricity as a result of the spontaneous reactions occurring inside it. 2. Electrolytic cell: is an electrochemical cell in which a non spontaneous reaction is driven by an external source of current.
Other important concepts include: Oxidation: the removal of electrons from a species. Reduction: the addition of electrons to a species. Redox reaction: a reaction in which there is a transfer of electrons from one species to another. Reducing agent: an electron donor in a redox reaction. Oxidizing agent: an electron acceptor in a redox reaction. • Two type of electrodes: Anode: the electrode at which oxidation occurs. Cathode: the electrode at which reduction occurs
Electrochemical cells • Liquid junction potential: due to the difference in the concentrations of electrolytes. • The right-hand side electrochemical cell is often expressed as follows: Zn(s)|ZnSO4(aq)||CuSO4(aq)|Cu(s) • The cathode reaction (copper ions being reduced to copper metal) is shown on the right. The double bar (||) represents the salt bridge that separates the two beakers, and the anode reaction is shown on the left: zinc metal is oxidized into zinc ions
In the above cell, we can trace the movement of charge. • Electrons are produced at the anode as the zinc is oxidized • The electrons flow though a wire, which we can use for electrical energy • The electrons move to the cathode, where copper ions are reduced. • The right side beaker builds up negative charge. Cl- ions flow from the salt bridge into the zinc solution and K+ ions flow into the copper solution to keep charge balanced. To write the half reaction for the above cell, Right-hand electrode: Cu2+(aq) + 2e- → Cu(s) Left-hand electrode: Zn2+(aq) + 2e- → Zn(s) The overall cell reaction can be obtained by subtracting left-hand reaction from the right-hand reaction: Cu2+(aq) + Zn(s) → Cu(s) + Zn2+(aq)
Expressing a reaction in terms of half-reactions Example : Express the formation of H2O from H2 and O2 in acidic solution as the difference of two reduction half-reactions. Redox couple: the reduced and oxidized species in a half-reaction such as Cu2+/Cu, Zn2+/Zn…. Ox + v e-→ Red The quotient is defined as: Q = aRed/aOx Example: Write the half-reaction and the reaction quotient for a chlorine gas electrode.
Notation of an electrochemical cell • Phase boundaries are denoted by a vertical bar. • A double vertical line, ||, denotes the interface that the junction potential has been eliminated. • Start from the anode.
Cell Potential • Cell potential: the potential difference between two electrodes of a galvanic cell (measured in volts V). • Maximum electrical work : we,max = ΔG • Electromotive force, E, • Relationship between E and ΔrG: ΔrG = -νFE where ν is the number of electrons that are exchanged during the balanced redox reaction and F is the Faraday constant, F = eNA. • At standard concentrations at 25oC, this equation can be written as ΔrGθ = -νFEθ