Copper galvanic cell

The zinc-copper galvanic cell is under standard conditions when the concentration of each ion is 1.00 M, as shown in Figure 19-13. The cell potential under these conditions can be determined by connecting the electrodes to a voltmeter. The measured potential is 1.10 V, with the Zn electrode at the higher (more negative) potential, so Zn gives up electrons and E eii = 1.10 V ... 

FIGURE 11.4 Polarization in zinc-copper galvanic cell. 

Cables with a copper sheathing are used only seldom. The protective cover is the same as with a corrugated steel-sheathed cable. If a cable with copper sheathing is connected to a lead-sheathed cable (A-PMbc) (see Table 13-1), the copper sheathing acts as a cathode in a galvanic cell and is therefore cathodically protected. 

Copper-base alloys will corrode in aerated conditions. It is, therefore, sometimes appropriate to consider cathodic protection. It becomes particularly relevant when the flow rates are high or when the design of an item causes the copper to be an anode in a galvanic cell (e.g. a copper alloy tube plate in a titanium-tubed heat exchanger). Corrosion can be controlled by polarisation to approximately — 0-6V (vs. CU/CUSO4) and may be achieved using soft iron sacrificial anodes. 

An interesting application of electrode potentials is to the calculation of the e.m.f. of a voltaic cell. One of the simplest of galvanic cells is the Daniell cell. It consists of a rod of zinc dipping into zinc sulphate solution and a strip of copper in copper sulphate solution the two solutions are generally separated by placing one inside a porous pot and the other in the surrounding vessel. The cell may be represented as ... 

From the chemical viewpoint, the galvanic cell is a current source in which a local separation of oxidation and reduction process exists. This is explained below by the example of the Daniell element (Fig. 3). Here the galvanic cell contains copper as the positive electrode, zinc as the nega-... 

An electrochemical cell in which electrolysis takes place is called an electrolytic cell. The arrangement of components in electrolytic cells is different from that in galvanic cells. Typically, the two electrodes share the same compartment, there is only one electrolyte, and concentrations and pressures are far front standard. As in all electrochemical cells, the current is carried through the electrolyte by the ions present. For example, when copper metal is refined electrolytically, the anode is impure copper, the cathode is pure copper, and the electrolyte is an aqueous solution of CuS04. As the Cu2f ions in solution are reduced and deposited as Cu atoms at the cathode, more Cu2+ ions migrate toward the cathode to take their place, and in turn their concentration is restored by Cu2+ produced by oxidation of copper metal at the anode. 

When two electrodes contain different amounts of excess charge, there is a difference in electrical potential between them. Because it has more excess electrons, the zinc electrode is at a higher electrical potential than the copper electrode. In a galvanic cell, the difference in electrical potential causes electrons to flow from a region where the concentration of electrons is higher to a region where the concentration of electrons is lower. In this case, eiectrons flow from the zinc electrode toward the copper electrode, as shown at the molecular level in Figure 19-12. 

It is found that the dissolution of zinc sulfides occurs more rapidly when they are in contact with copper sulfide or iron sulfide than when the sulfides of these types are absent. This enhancement is brought about by the formation of a galvanic cell. When two sulfide minerals are in contact, the condition for dissolution in acidic medium of one of the sulfides is that it should be anodic to the other sulfide in contact. This is illustrated schematically in Figure 5.3 (A). Thus, pyrite behaves cathodically towards several other sulfide minerals such as zinc sulfide, lead sulfide and copper sulfide. Consequently, pyrite enhances the dissolution of the other sulfide minerals while these minerals themselves understandably retard the dissolution of pyrite. This explains generally the different leaching behavior of an ore from different locations. The ore may have different mineralogical composition. A particle of sphalerite (ZnS) in contact with a pyrite particle in an aerated acid solution is the right system combination for the sphalerite to dissolve anodically. The situation is presented below ... 

It is instructive at the present stage to study the comparison of zinc and copper electrodes against the hydrogen electrode in order to delineate the very basic and centrally important ingredients on which the essence of electrochemistry is based. For this purpose, a galvanic cell is assembled to study the reaction as shown below ... 

The dissolution of zinc in a mineral acid is much faster when the zinc contains an admixture of copper. This is because the surface of the metal contains copper crystallites at which hydrogen evolution occurs with a much lower overpotential than at zinc (see Fig. 5.54C). The mixed potential is shifted to a more positive value, E mix, and the corrosion current increases. In this case the cathodic and anodic processes occur on separate surfaces. This phenomenon is termed corrosion of a chemically heterogeneous surface. In the solution an electric current flows between the cathodic and anodic domains which represent short-circuited electrodes of a galvanic cell. A. de la Rive assumed this to be the only kind of corrosion, calling these systems local cells. 

Danlell cell a galvanic cell composed of copper/copperGI) ion and zinc/zinc ion half-cells. 

Galvanic (voltaic) cells produce electricity by using a redox reaction. Let s take that zinc/copper redox reaction that we studied before (the direct electron transfer one) and make it a galvanic cell by separating the oxidation and reduction half-reactions. 

This reaction occurs on the surface of the zinc strip, where electrons are transferred from zinc atoms to copper(II) ions when these atoms and ions are in direct contact. A common technological invention called a galvanic cell uses redox reactions, such as the one described above, to release energy in the form of electricity. 

Figure 11.1 shows one example of a galvanic cell, called the Daniell cell. One half of the cell consists of a piece of zinc placed in a zinc sulfate solution. The other half of the cell consists of a piece of copper placed in a copper(II) sulfate solution. A porous barrier, sometimes called a semi-permeable membrane, separates these two half-cells. It stops the copper(II) ions from coming into direct contact with the zinc electrode. 

The zinc anode and copper cathode of a Daniell cell are both metals, and can act as electrical conductors. However, some redox reactions involve substances that cannot act as electrodes, such as gases or dissolved electrolytes. Galvanic cells that involve such redox reactions use inert electrodes. An inert electrode is an electrode made from a material that is neither a reactant nor a product of the cell reaction. Figure 11.6 shows a cell that contains one inert electrode. The chemical equation, net ionic equation, and half-reactions for this cell are given below. 

In the galvanic cell, the zinc anode gradually dissolves. The copper cathode grows as more copper is deposited onto it. In the electrolytic cell, the copper anode gradually dissolves. The zinc cathode grows as more zinc is deposited onto it. The process in which a metal is deposited, or plated, onto the cathode in an electrolytic cell is known as electroplating. Electroplating is very important in industry, as you will learn later in this chapter. 

Sometimes, the rusting of iron is promoted accidentally. For example, by connecting an iron pipe to a copper pipe in a plumbing system, an inexperienced plumber could accidentally speed up tbe corrosion of tbe iron pipe. Copper is less reactive than iron. Therefore, copper acts as the cathode and iron as the anode in numerous small galvanic cells at the intersection of the two pipes. 

The galvanic cell pictured in Figure 7.1 is not at equilibrium. If switch S is closed, electrons will spontaneously flow from the zinc (anode) to the copper (cathode) electrode. This flow will continue imtil the reactants and products attain their equilibrium concentrations. If switch S is opened before the cell reaches equilibrium, the electron flow will be interrupted. The voltmeter would register a positive voltage, which is a measure of the degree to which the redox reaction drives electrons from the anode to the cathode. Since this voltage is a type of energy that has the potential to do work, it is referred to as a redox potential or cell potential, denoted as... 

Electrochemical Reactions. Consider a simple galvanic cell, composed of two metal electrodes, zinc and copper, immersed in two different aqueous solutions of unit activity—in this case, 1.0 M ZnS04 and 1.0 M CUSO4, respectively, connected by an electrical circuit, and separated by a semipermeable membrane (see Figure 3.8). The membrane allows passage of ions, but not bulk flow of the aqueous solutions from one side of the cell to the other. Electrons are liberated at the anode by the oxidation (increase in the oxidation number) of the zinc electrode ... 

The voltage we measure is characteristic of the metals we use. As an additional example, unit activity solutions of CuCE and AgCl with copper and silver electrodes, respectively, give a potential difference of about 0.45 V. We could continue with this type of measurement for aU the different anode-cathode combinations, but the number of galvanic cells needed would be very large. Fortunately, the half-reactions for most metals have been calculated relative to a standard reference electrode, which is arbitrarily selected as the reduction of hydrogen ... 

Rg. 7.14. A galvanic cell composed of a copper electrode in cupric ion solution and a standard hydrogen electrode (a) gives a measurable potential difference Ee (b). 

The following items are obtained from the stockroom for the construction of a galvanic cell two 250-mL beakers and a salt bridge, a voltmeter with attached wires and clips, 200 mL of 0.010 M CrCl3(aq) solution, 200 mL of 0.16 M CuS04(aq) solution, a piece of copper wire, and a chrome-plated piece of metal, (a) Describe the construction of the galvanic cell. 

---