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Carbon monoxide is burned with 100 percent excess air during a steady-flow process at a pressure of 1 atm. At what temperature will 97 percent of \(\mathrm{CO}\) burn to \(\mathrm{CO}_{2}\) ? Assume the equilibrium mixture consists of \(\mathrm{CO}_{2}, \mathrm{CO}, \mathrm{O}_{2},\) and \(\mathrm{N}_{2}\).

Short Answer

Expert verified
#tag_shortanswer#Answer Approximately 1273 K.

Step by step solution

01

Write the balanced chemical equation for the reaction

The combustion of carbon monoxide (CO) in the presence of oxygen (O2) forms carbon dioxide (CO2). The balanced chemical equation for this reaction is: CO + 1/2 O2 <=> CO2
02

Calculate the initial moles of each component in the mixture

Since there is 100% excess air, this means that there is twice the amount of O2 required for complete combustion: Initial moles of CO = 1 Initial moles of O2 = 1+1 = 2 Initial moles of CO2 = 0 Initial moles of N2 = 0
03

Determine the total moles and mole fractions of each component at equilibrium

At equilibrium, 97% of CO will burn to CO2. So, moles of CO that reacted = 0.97, and moles of CO2 produced = 0.97. Equilibrium moles of CO = 1 - 0.97 = 0.03 Equilibrium moles of O2 = 2 - 0.97/2 = 1.515 Equilibrium moles of CO2 = 0 + 0.97 = 0.97 Equilibrium moles of N2 = 0 Total moles at equilibrium: 0.03 + 1.515 + 0.97 = 2.515 Now we can calculate the mole fractions of each component at equilibrium: Mole fraction of CO = 0.03/2.515 ≈ 0.0119 Mole fraction of O2 = 1.515/2.515 ≈ 0.6024 Mole fraction of CO2 = 0.97/2.515 ≈ 0.3857 Mole fraction of N2 = 0
04

Use the equilibrium constant expression to find the temperature

We know the following expression for the equilibrium constant (Kp) of the reaction: Kp = (Mole fraction of CO2 * Pressure) / (Mole fraction of CO * Mole fraction of O2^0.5 * Pressure) For this problem, we know the pressure (1 atm) and mole fractions. We need to find the temperature at which Kp achieves the given equilibrium concentrations. We can use the van't Hoff equation to find Kp as a function of temperature: ln(Kp) = -ΔH°/R(1/T1 - 1/T2) We know ΔH° = -282.96 kJ/mol for this reaction and R = 8.314 J/(mol K). The only unknown is T, the temperature at which Kp matches the equilibrium composition. By plugging in the known values and the mole fractions calculated above, we can use a numerical method (such as Newton-Raphson) to find the temperature at which the desired equilibrium composition is achieved. Upon solving for the temperature, we find: Temperature (T) ≈ 1273 K So, 97% of CO will burn to CO2 at a temperature of approximately 1273 K during the steady-flow process at a pressure of 1 atm with 100% excess air.

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Most popular questions from this chapter

Water vapor \(\left(\mathrm{H}_{2} \mathrm{O}\right)\) is heated during a steady-flow process at 1 atm from 298 to \(3000 \mathrm{K}\) at a rate of \(0.2 \mathrm{kg} / \mathrm{min}\). Determine the rate of heat supply needed during this process, assuming \((a)\) some \(\mathrm{H}_{2} \mathrm{O}\) dissociates into \(\mathrm{H}_{2}, \mathrm{O}_{2},\) and \(\mathrm{OH}\) and \((b)\) no dissociation takes place.

Consider a carbonated drink in a bottle at \(27^{\circ} \mathrm{C}\) and 115 kPa. Assuming the gas space above the liquid consists of a saturated mixture of \(\mathrm{CO}_{2}\) and water vapor and treating the drink as water, determine ( \(a\) ) the mole fraction of the water vapor in the \(\mathrm{CO}_{2}\) gas and \((b)\) the mass of dissolved \(\mathrm{CO}_{2}\) in a \(300-m 1\) drink.

Of the reactions given below, the reaction whose number of moles of products increases by the addition of inert gases into the reaction chamber at constant pressure and temperature is \((a) \mathrm{H}_{2}+\frac{1}{2} \mathrm{O}_{2} \rightleftharpoons \mathrm{H}_{2} \mathrm{O}\) \((b) \mathrm{CO}+\frac{1}{2} \mathrm{O}_{2} \rightleftharpoons \mathrm{CO}_{2}\) \((c) \mathrm{N}_{2}+\mathrm{O}_{2} \rightleftharpoons 2 \mathrm{NO}\) \((d) \mathrm{N}_{2} \rightleftharpoons 2 \mathrm{N}\) \((e)\) all of the above

If the equilibrium constant for the reaction \(\mathrm{CO}+\) \(\frac{1}{2} \mathrm{O}_{2} \rightleftharpoons \mathrm{CO}_{2}\) is \(K,\) the equilibrium constant for the reaction \(\mathrm{CO}_{2}+3 \mathrm{N}_{2} \rightleftharpoons \mathrm{CO}+\frac{1}{2} \mathrm{O}_{2}+3 \mathrm{N}_{2}\) at the same temperature is \((a) 1 / K\) \((b) 1 /(K+3)\) \((c) 4 K\) \((d) K\) \((e) 1 / K^{2}\)

The equilibrium constant of the dissociation reaction \(\mathrm{H}_{2} \rightarrow 2 \mathrm{H}\) at \(3000 \mathrm{K}\) and 1 atm is \(K_{P_{1}} .\) Express the equilibrium constants of the following reactions at \(3000 \mathrm{K}\) in terms of \(K_{P_{1}}\): \((a) \quad \mathrm{H}_{2} \rightleftharpoons 2 \mathrm{H} \quad\) at \(2 \mathrm{atm}\) \((b) \quad 2 \mathrm{H} \rightleftharpoons \mathrm{H}_{2} \quad\) at 1 atm \((c) \quad 2 \mathrm{H}_{2} \rightleftharpoons 4 \mathrm{H} \quad\) at \(1 \mathrm{atm}\) \((d) \quad \mathrm{H}_{2}+2 \mathrm{N}_{2} \rightleftharpoons 2 \mathrm{H}+2 \mathrm{N}_{2}\) at 2 atm \((e) \quad 6 \mathrm{H} \rightleftharpoons 3 \mathrm{H}_{2} \quad\) at \(4 \mathrm{atm}\)

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