Chapter 23: Problem 34
Distinguish between substitutional and interstitial alloys. What conditions favor formation of substitutional alloys?
Chapter 23: Problem 34
Distinguish between substitutional and interstitial alloys. What conditions favor formation of substitutional alloys?
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Get started for freeConsider the thermodynamics of calcination. (a) The following equation is a generic reaction representing calcination of a metal carbonate: $$\mathrm{MCO}_{3}(s) \longrightarrow \mathrm{MO}(s)+\mathrm{CO}_{2}(g)$$ Would you expect this reaction to become more or less spontaneous as the temperature increases? (b) What is the standard free energy, \(\Delta G^{\circ}\), for the reaction corresponding to the calcination of \(\mathrm{PbCO}_{3}\) (Equation 23.1) at \(25^{\circ} \mathrm{C}\) under standard conditions? Is this reaction spontaneous? If not, at what temperature does this reaction become spontaneous (assuming \(\Delta H^{\circ}\) and \(S^{\circ}\) values do not change with temperature)?
The element vanadium exhibits multiple oxidation states in its compounds, including \(+2\). The compound \(\mathrm{VCl}_{2}\) is known, whereas \(\mathrm{ScCl}_{2}\) is unknown. Use electron configurations and effective nuclear charges to account for this difference in behavior.
(a) In the basic oxygen process for steel formation, what reactions cause the temperature in the converter to increase? (b) Write balanced chemical equations for the oxidation of carbon, sulfur, and silicon in the converter.
The reduction of metal oxides is often accomplished using carbon monoxide as a reducing agent. Carbon (coke) and carbon dioxide are usually present, leading to the following reaction: $$\mathrm{C}(\mathrm{s})+\mathrm{CO}_{2}(g) \rightleftharpoons 2 \mathrm{CO}(g)$$ Using data from Appendix \(\mathrm{C}\), calculate the equilibrium constant for this reaction at \(298 \mathrm{~K}\) and at \(2000 \mathrm{~K}\), assuming that the enthalpies and entropies of formation do not depend upon temperature.
Write balanced chemical equations that correspond to the steps in the following brief account of the metallurgy of molybdenum: Molybdenum occurs primarily as the sulfide, \(\mathrm{MoS}_{2}\). On boiling with concentrated nitric acid, a white residue of \(\mathrm{MoO}_{3}\) is obtained. This is an acidic oxide; when it is dissolved in excess hot concentrated ammonia, ammonium molybdate crystallizes on cooling. On heating ammonium molybdate, white \(\mathrm{MoO}_{3}\) is obtained. On further heating to \(1200^{\circ} \mathrm{C}\) in hydrogen, a gray powder of metallic molybdenum is obtained.
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