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A mixture of copper and gold metals that is subjected to electrorefining contains tellurium as an impurity. The standard reduction potential between tellurium and its lowest common oxidation state, \(\mathrm{Te}^{4+},\) is $$ \mathrm{Te}^{4+}(a q)+4 \mathrm{e}^{-} \longrightarrow \mathrm{Te}(s) \quad E_{\mathrm{red}}^{\circ}=0.57 \mathrm{V} $$ Given this information, describe the probable fate of tellurium impurities during electrorefining. Do the impurities fall to the bottom of the refining bath, unchanged, as copper is oxidized, or do they go into solution as ions? If they go into solution, do they plate out on the cathode?

Short Answer

Expert verified
During the electrorefining process, tellurium impurities will go into the solution as Te^(4+) ions, and they'll likely plate out on the cathode as they have a higher standard reduction potential than copper (0.57 V) but lower than gold (1.50 V).

Step by step solution

01

Understand the electrorefining process

Electrorefining is a process that involves applying an electrical current to dissolve and purify metals. An anode (positive electrode) made of impure metal is put into an electrolyte solution containing metal ions. A cathode (negative electrode) is placed in the same solution. The metal ions in the solution are attracted to the cathode, where they gain electrons and are reduced to metal atoms. These metal atoms build up on the cathode, while the impurities either fall to the bottom or stay in the solution.
02

Compare the standard reduction potentials

To determine the behavior of tellurium during electrorefining, we need to compare the standard reduction potentials (E°) of copper (Cu), gold (Au), and tellurium (Te). The given standard reduction potential of tellurium is: \[ \mathrm{Te}^{4+}(a q)+4 \mathrm{e}^{-} \longrightarrow \mathrm{Te}(s) \quad E_{\mathrm{red}}^{\circ}=0.57 \mathrm{V} \] Now let's look up the standard reduction potentials for copper and gold. They are: Copper: \[ \mathrm{Cu}^{2+}(a q)+2 \mathrm{e}^{-} \longrightarrow \mathrm{Cu}(s) \quad E_{\mathrm{red}}^{\circ}=0.34 \mathrm{V} \] Gold: \[ \mathrm{Au}^{3+}(a q)+3 \mathrm{e}^{-} \longrightarrow \mathrm{Au}(s) \quad E_{\mathrm{red}}^{\circ}=1.50 \mathrm{V} \]
03

Determine the fate of tellurium impurities

During the electrorefining process, metals with lower reduction potentials (more negative) are easier to oxidize and dissolve, while metals with higher reduction potentials (more positive) are more readily reduced and plated out on the cathode. To determine the fate of tellurium, it's important to compare its reduction potential with those of copper and gold: - Te: E° = 0.57 V - Cu: E° = 0.34 V - Au: E° = 1.50 V Since Te has a higher standard reduction potential than Cu but lower than Au, Te is more readily oxidized (goes into solution as ions) than Au and more likely to be reduced (plated out) than Cu. Thus, we can conclude that tellurium impurities will go into the solution as Te^(4+) ions, and they'll likely plate out on the cathode during the electrorefining process.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Standard Reduction Potential
When studying electrochemistry, the standard reduction potential (E°) is a key concept, as it helps us predict the behavior of elements in an electrolytic process.

Standard reduction potential is a measure of the tendency of a chemical species to be reduced, and it's represented by a voltage value. When comparing different substances, those with more positive E° values have a greater likelihood of gaining electrons and becoming reduced. In contrast, substances with more negative E° values tend to lose electrons and undergo oxidation.

In the context of electrorefining, by comparing the E° values of different metals, we can determine which metal will be deposited, or plated, onto the cathode. Metals with higher E° values plate onto the cathode preferentially, as they are more likely to gain electrons from the cathode.
Oxidation States
Understanding oxidation states is essential for explaining chemical reactions, especially in electrorefining. An oxidation state indicates the degree of oxidation of an atom within a compound. It is represented by a numerical value that can be positive, zero, or negative.

In the given exercise, we are considering Tellurium (Te) in its +4 oxidation state, denoted as Te^(4+). Oxidation states allow us to write and balance chemical equations accurately. They also help in determining how electrons are transferred in a redox reaction, which is the basis of the electrorefining process. An atom's oxidation state helps predict how it will interact when electrical current is applied: whether it will lose electrons and dissolve into the solution or gain electrons and precipitate onto the electrode.
Metal Purification
The process of refining and purifying metals is fundamental in obtaining materials with the desired levels of purity for industrial applications. Metal purification, like electrorefining, employs the principles of electrochemistry to separate pure metals from their impurities.

During electrorefining, an electrical current is used to transfer metal ions from an impure anode to a pure cathode submerged in an electrolyte solution. Impurities with different reduction potentials either remain in the electrolyte, dissolve, or collect at the bottom as sludges, depending on their nature and their reaction to the electrical current.

The efficiency of this process is influenced by various factors, including the relative standard reduction potentials of the metals involved, ensuring that the desired metal is deposited at the cathode, while impurities are removed, resulting in a high-purity final product.

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Most popular questions from this chapter

(a) \(\mathrm{A} \mathrm{Cr}^{3+}(a q)\) solution is electrolyzed, using a current of 7.60 \(\mathrm{A} .\) What mass of \(\mathrm{Cr}(s)\) is plated out after 2.00 days? (b) What amperage is required to plate out 0.250 mol Cr from a \(\mathrm{Cr}^{3+}\) solution in a period of 8.00 \(\mathrm{h} ?\)

Gold exists in two common positive oxidation states, \(+1\) and \(+3 .\) The standard reduction potentials for these oxidation states are $$ \begin{array}{ll}{\mathrm{Au}^{+}(a q)+\mathrm{e}^{-}} \quad {\longrightarrow \mathrm{Au}(s) \quad E_{\mathrm{red}}^{\circ}=+1.69 \mathrm{V}} \\\ {\mathrm{Au}^{3+}(a q)+3 \mathrm{e}^{-} \longrightarrow \mathrm{Au}(s)} \quad {E_{\mathrm{red}}^{\circ}=+1.50 \mathrm{V}}\end{array} $$ (a) Can you use these data to explain why gold does not tarnish in the air? ( b) Suggest several substances that should be strong enough oxidizing agents to oxidize gold metal. (c) Miners obtain gold by soaking gold-containing ores in an aqueous solution of sodium cyanide. A very soluble complex ion of gold forms in the aqueous solution because of the redox reaction $$ \begin{array}{rl}{4 \mathrm{Au}(s)+8 \mathrm{NaCN}(a q)+2} & {\mathrm{H}_{2} \mathrm{O}(l)+\mathrm{O}_{2}(g)} \\ {\longrightarrow} & {4 \mathrm{Na}\left[\mathrm{Au}(\mathrm{CN})_{2}\right](a q)+4 \mathrm{NaOH}(a q)}\end{array} $$ What is being oxidized, and what is being reduced in this reaction? (d) Gold miners then react the basic aqueous product solution from part (c) with Zn dust to get gold metal. Write a balanced redox reaction for this process. What is being oxidized, and what is being reduced?

A cell has a standard cell potential of \(+0.177 \mathrm{V}\) at 298 \(\mathrm{K}\) . What is the value of the equilibrium constant for the reaction ( a ) if \(n=1 ?(\mathbf{b})\) if \(n=2 ?(\mathbf{c})\) if \(n=3 ?\)

A voltaic cell utilizes the following reaction: $$ \mathrm{Al}(s)+3 \mathrm{Ag}^{+}(a q) \longrightarrow \mathrm{Al}^{3+}(a q)+3 \mathrm{Ag}(s) $$ What is the effect on the cell emf of each of the following changes? (a) Water is added to the anode half-cell, diluting the solution. (b) The size of the aluminum electrode is increased. (c) A solution of AgNO \(_{3}\) is added to the cathode half-cell, increasing the quantity of Ag' but not changing its concentration. (d) HCl is added to the AgNO\(_{3}\) solution precipitating some of the Ag' as AgCl.

Using the standard reduction potentials listed in Appendix E, calculate the equilibrium constant for each of the following reactions at \(298 \mathrm{K} :\) $$ \begin{array}{l}{\text { (a) } \mathrm{Fe}(s)+\mathrm{Ni}^{2+}(a q) \longrightarrow \mathrm{Fe}^{2+}(a q)+\mathrm{Ni}(s)} \\ {\text { (b) } \mathrm{Co}(s)+2 \mathrm{H}^{+}(a q) \longrightarrow \mathrm{Co}^{2+}(a q)+\mathrm{H}_{2}(g)} \\ {\text { (c) } 10 \mathrm{Br}^{-}(a q)+2 \mathrm{MnO}_{4}^{-}(a q)+16 \mathrm{H}^{+}(a q) \rightarrow} \\ {\quad 2 \mathrm{Mn}^{2+}(a q)+8 \mathrm{H}_{2} \mathrm{O}(l)+5 \mathrm{Br}_{2}(l)}\end{array} $$

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