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How does the tendency of iron to rust depend on the pH of the solution?

Short Answer

Expert verified
Iron rusts more in acidic solutions and less in basic solutions.

Step by step solution

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01

Understanding Iron Rusting

Iron rusts when it reacts with oxygen in the presence of water or moisture, forming iron oxide (rust). The rate of rusting is influenced by the pH of the solution.
02

Analyzing pH Influence

The pH level of a solution indicates its acidity or basicity. Low pH levels (acidic conditions) promote rusting, whereas high pH levels (basic conditions) inhibit rusting. Neutral conditions (pH=7) allow rusting at a moderate rate.
03

Applying Chemistry Knowledge

In acidic solutions (pH < 7), hydrogen ions ( H^+ ) can facilitate the oxidation of iron, speeding up rust formation. In basic solutions (pH > 7), hydroxide ions ( OH^- ) tend to react with iron to form protective complexes, slowing rusting.
04

Conclusion on pH and Rust

Overall, as the pH decreases (more acidic), the tendency for iron to rust increases. As the pH increases (more basic), the tendency for iron to rust decreases.

Key Concepts

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

pH influence
The pH of a solution is a scale used to specify its acidity or basicity. This scale ranges from 0 to 14, where a pH of 7 is considered neutral, less than 7 indicates acidity, and greater than 7 indicates basicity. The pH of the environment significantly impacts the rate and likelihood of iron rusting. In acidic solutions, rusting occurs more quickly, while basic solutions slow down the rusting process. Understanding this concept is crucial, especially for preventing corrosion in various environments. Therefore, by managing the pH levels, it is possible to either accelerate or decelerate the rate of iron oxidation.
oxidation of iron
Oxidation is a chemical process where an element loses electrons. In the case of iron, oxidation occurs when iron atoms give up electrons to oxygen, resulting in iron oxide, commonly known as rust. This phenomenon is what you observe when metal corrodes or rusts. The presence of water (moisture) is critical, as it facilitates the movement of electrons from iron to oxygen. This is why iron tends to rust faster in damp conditions. The chemistry unfolds as follows: iron gives electrons to oxygen, forming iron(II) or iron(III) oxides, which are the compounds responsible for the reddish-brown appearance of rust. In environments with varying pH levels, the extent and rate of this oxidation process drastically change.
acidic conditions
In acidic conditions where the pH is less than 7, there are many hydrogen ions ( H^+ ) present. These hydrogen ions play a substantial role in prompting the oxidation process of iron. They react with iron and assist in breaking it down into iron ions and free electrons, which then combine with water and oxygen to form rust. Acidic environments, therefore, expedite rusting.
  • More hydrogen ions lead to quicker electron transfer from iron.
  • This accelerates the formation of iron oxide.
  • Examples include industrial zones where pollution can lower pH and expedite rusting.
This is a critical factor to consider in protecting iron objects and structures from corrosion.
basic conditions
When the solution is basic, with a pH greater than 7, hydroxide ions ( OH^- ) are abundant. These ions react with iron differently compared to acidic environments. Instead of promoting the breakdown of iron, they form iron hydroxide. This compound can create a protective film around the iron surface, slowing down further corrosion and rust formation.
  • High pH leads to the formation of iron hydroxide.
  • This acts as a barrier against oxygen and water.
  • Such environments include areas treated with protective coatings or alkaline cleaning agents.
By maintaining basic conditions, the longevity of iron structures can be significantly enhanced, illustrating the importance of controlling pH to prevent rusting.

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Most popular questions from this chapter

Consider a galvanic cell composed of the SHE and a half-cell using the reaction \(\mathrm{Ag}^{+}(a q)+e^{-} \longrightarrow \mathrm{Ag}(s)\). (a) Calculate the standard cell potential. (b) What is the spontaneous cell reaction under standard-state conditions? (c) Calculate the cell potential when \(\left[\mathrm{H}^{+}\right]\) in the hydrogen electrode is changed to (i) \(1.0 \times 10^{-2} M\) and (ii) \(1.0 \times 10^{-5} M\), all other reagents being held at standard- state conditions. (d) Based on this cell arrangement, suggest a design for a pH meter.

Calculate the standard potential of the cell consisting of the \(\mathrm{Zn} / \mathrm{Zn}^{2+}\) half-cell and the SHE. What will the emf of the cell be if \(\left[\mathrm{Zn}^{2+}\right]=0.45 \mathrm{M}, P_{\mathrm{H}_{2}}=2.0 \mathrm{~atm},\) and \(\left[\mathrm{H}^{+}\right]=1.8 M ?\)

From the following information, calculate the solubility product of \(\mathrm{AgBr}\) : $$ \begin{array}{ll} \mathrm{Ag}^{+}(a q)+e^{-} \longrightarrow \mathrm{Ag}(s) & E^{\circ}=0.80 \mathrm{~V} \\ \mathrm{AgBr}(s)+e^{-} \longrightarrow \mathrm{Ag}(s)+\mathrm{Br}^{-}(a q) & E^{\circ}=0.07 \mathrm{~V} \end{array} $$

Define the following terms: anode, cathode, cell voltage, electromotive force, standard reduction potential.

A piece of magnesium ribbon and a copper wire are partially immersed in a \(0.1 M \mathrm{HCl}\) solution in a beaker. The metals are joined externally by another piece of metal wire. Bubbles are seen to evolve at both the \(\mathrm{Mg}\) and Cu surfaces. (a) Write equations representing the reactions occurring at the metals. (b) What visual evidence would you seek to show that Cu is not oxidized to \(\mathrm{Cu}^{2+} ?(\mathrm{c})\) At some stage, \(\mathrm{NaOH}\) solution is added to the beaker to neutralize the HCl acid. Upon further addition of \(\mathrm{NaOH},\) a white precipitate forms. What is it?

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