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The fuel in high-efficiency natural gas vehicles consists primarily of methane \(\left(\mathrm{CH}_{4}\right) .\) (a) How much heat is produced in burning 1 mol of \(\mathrm{CH}_{4}(g)\) under standard conditions if reactants and products are brought to \(298 \mathrm{~K}\) and \(\mathrm{H}_{2} \mathrm{O}(l)\) is formed? (b) What is the maximum amount of useful work that can be accomplished under standard conditions by this system?

Short Answer

Expert verified
The heat produced in burning 1 mol of CH4(g) is 965.1 kJ/mol, and the maximum amount of useful work that can be accomplished under standard conditions by this system is 884.3 kJ/mol.

Step by step solution

01

Determine the balanced chemical equation for the combustion of CH4

Using the formula for the combustion of a hydrocarbon, we can find the balanced chemical equation for the combustion of CH4: CH4 (g) + 2 O2 (g) -> CO2 (g) + 2 H2O (l)
02

Find the standard enthalpy change of the reaction

We can calculate the standard enthalpy change of the reaction (∆H°) as follows: ∆H° = [n * ∆H°f(products)] - [n * ∆H°f(reactants)] Standard enthalpy of formation (∆H°f) values for the compounds are as follows: ∆H°f(CH4 (g)) = -74.8 kJ/mol ∆H°f(O2 (g)) = 0 kJ/mol (since it's an element in its standard state) ∆H°f(CO2 (g)) = -393.5 kJ/mol ∆H°f(H2O (l)) = -285.8 kJ/mol Now, we can calculate ∆H° for the reaction: ∆H° = [1(-393.5) + 2(-285.8)] - [1(-74.8) + 2(0)] ∆H° = (-393.5 - 2 * 285.8) - (-74.8) ∆H° = -965.1 kJ/mol The heat produced in burning 1 mol of CH4(g) is 965.1 kJ/mol.
03

Calculate the standard Gibbs free energy change of the reaction

Now we need to find the standard Gibbs free energy change of the reaction (∆G°) to determine the maximum amount of useful work that can be accomplished under standard conditions. We can do this by using the following equation: ∆G° = ∆H° - T∆S° First, we need to find the standard entropy change (∆S°) for the reaction: ∆S° = [n * S°(products)] - [n * S°(reactants)] Standard molar entropy (S°) values for the compounds are as follows: S°(CH4 (g)) = 186.3 J/mol·K S°(O2 (g)) = 205.2 J/mol·K S°(CO2 (g)) = 213.8 J/mol·K S°(H2O (l)) = 69.9 J/mol·K Now, we can calculate ∆S° for the reaction: ∆S° = [1(213.8) + 2(69.9)] - [1(186.3) + 2(205.2)] ∆S° = (213.8 + 2 * 69.9) - (186.3 + 410.4) ∆S° = -270.8 J/mol·K Now we can calculate the ∆G° for the reaction at 298 K: ∆G° = ∆H° - T∆S° ∆G° = -965.1 kJ/mol - (298 K)(-270.8 J/mol·K) / 1000 (to convert J to kJ) ∆G° = -965.1 kJ/mol + 80.8 kJ/mol ∆G° = -884.3 kJ/mol The maximum amount of useful work that can be accomplished under standard conditions by this system is 884.3 kJ/mol.

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Key Concepts

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

Standard Enthalpy Change
Standard enthalpy change, represented as \( \Delta H^\circ \), is a fundamental concept in chemical thermodynamics. It refers to the heat absorbed or released during a chemical reaction when all reactants and products are in their standard states. Values are measured under standard conditions, typically at 298 K and 1 atm pressure.

For the combustion of methane, \( \Delta H^\circ \) is calculated using the enthalpy of formation values of the involved compounds. Methane, water, and carbon dioxide each have specific enthalpy values that need to be plugged into the equation:
  • \( \Delta H^\circ(\text{CH}_4 (g)) = -74.8 \text{ kJ/mol} \)
  • \( \Delta H^\circ(\text{O}_2 (g)) = 0 \text{ kJ/mol} \)
  • \( \Delta H^\circ(\text{CO}_2 (g)) = -393.5 \text{ kJ/mol} \)
  • \( \Delta H^\circ(\text{H}_2\text{O} (l)) = -285.8 \text{ kJ/mol} \)
Using these values, we determine the overall enthalpy change as \(-965.1 \text{ kJ/mol}\). This indicates a significant release of heat energy, revealing why methane is an efficient fuel.
Standard Gibbs Free Energy
The standard Gibbs free energy change \( \Delta G^\circ \) helps us understand a reaction's spontaneity and the maximum work it can perform. A negative \( \Delta G^\circ \) indicates a spontaneous reaction at constant temperature and pressure. To calculate \( \Delta G^\circ \), use the equation:
  • \( \Delta G^\circ = \Delta H^\circ - T\Delta S^\circ \)
In the methane combustion example:
  • \( \Delta H^\circ = -965.1 \text{ kJ/mol} \)
  • \( T = 298 \text{ K} \)
  • \( \Delta S^\circ = -270.8 \text{ J/mol}\cdot\text{K} = -0.2708 \text{ kJ/mol}\cdot\text{K} \)
After calculation, we find \( \Delta G^\circ = -884.3 \text{ kJ/mol} \), confirming the reaction is highly spontaneous and could produce a significant amount of work, crucial for natural gas vehicles.
Standard Entropy Change
Standard entropy change \( \Delta S^\circ \) provides insight into the disorder or randomness in a system during a reaction. Higher entropy typically means more disorder.

In chemical thermodynamics, reactions tend toward states that increase entropy. For the methane combustion reaction, \( \Delta S^\circ \) is negative, calculated using the standard molar entropies:
  • \( S^\circ(\text{CH}_4 (g)) = 186.3 \text{ J/mol}\cdot\text{K} \)
  • \( S^\circ(\text{O}_2 (g)) = 205.2 \text{ J/mol}\cdot\text{K} \)
  • \( S^\circ(\text{CO}_2 (g)) = 213.8 \text{ J/mol}\cdot\text{K} \)
  • \( S^\circ(\text{H}_2\text{O} (l)) = 69.9 \text{ J/mol}\cdot\text{K} \)
With a calculated \( \Delta S^\circ \) of \(-270.8 \text{ J/mol}\cdot\text{K} \), it suggests the system becomes less disordered. The gases form liquid water, a more ordered state.
Natural Gas Vehicles
Natural gas vehicles (NGVs) run on compressed natural gas (CNG), primarily composed of methane. Methane's efficient combustion makes it an ideal fuel source, releasing less greenhouse gas than gasoline or diesel.

The benefits of using NGVs include:
  • Lower emissions contributing to cleaner air
  • Cost efficiency due to cheaper fuel prices
  • Widespread availability of natural gas resources
  • Silent operation and smooth driving experience
By leveraging the combustion process of methane, NGVs epitomize the practical application of chemical thermodynamics in reducing environmental impact while enhancing fuel efficiency.
Chemical Thermodynamics
Chemical thermodynamics studies energy changes, particularly heat and work, in chemical reactions. It provides a structured way to understand how and why reactions occur, combining endothermic, exothermic, and energy releases.

Key areas include:
  • Understanding reaction spontaneity using Gibbs free energy
  • Predicting reaction heat flow through enthalpy
  • Assessing system order with entropy changes
  • Applying energy principles to real-world applications, like engines and power generation
Chemical thermodynamics not only explains basic scientific principles but also frames their practical applications, such as in NGVs where efficient energy conversion is crucial for design and function.

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Most popular questions from this chapter

Consider a system consisting of an ice cube. (a) Under what conditions can the ice cube melt reversibly? (b) If the ice cube melts reversibly, is \(\Delta E\) zero for the process? Explain.

A standard air conditioner involves a refrigerant that is typically now a fluorinated hydrocarbon, such as \(\mathrm{CH}_{2} \mathrm{~F}_{2}\). An air- conditioner refrigerant has the property that it readily vaporizes at atmospheric pressure and is easily compressed to its liquid phase under increased pressure. The operation of an air conditioner can be thought of as a closed system made up of the refrigerant going through the two stages shown here (the air circulation is not shown in this diagram). During expansion, the liquid refrigerant is released into an expansion chamber at low pressure, where it vaporizes. The vapor then undergoes compression at high pressure back to its liquid phase in a compression chamber. (a) What is the sign of \(q\) for the expansion? (b) What is the sign of \(q\) for the compression? (c) In a central air-conditioning system, one chamber is inside the home and the other is outside. Which chamber is where, and why? (d) Imagine that a sample of liquid refrigerant undergoes expansion followed by compression, so that it is back to its original state. Would you expect that to be a reversible process? (e) Suppose that a house and its exterior are both initially at \(31^{\circ} \mathrm{C}\). Some time after the air conditioner is turned on, the house is cooled to \(24^{\circ} \mathrm{C}\). Is this process spontaneous or nonspontaneous?

Consider a reaction $\mathrm{A}_{2}(g)+\mathrm{B}_{2}(g) \rightleftharpoons 2 \mathrm{AB}(g),$ with atoms of A shown in red in the diagram and atoms of \(\mathrm{B}\) shown in blue. (a) If \(K_{\mathrm{c}}=1,\) which box represents the system at equilibrium? (b) If \(K_{\mathrm{c}}=1,\) which box represents the system at \(Q < K_{\mathrm{c}} ?(\mathbf{c})\) Rank the boxes in order of increasing magnitude of \(\Delta G\) for the reaction. [ Sections 19.5 and 19.7\(]\)

(a) What sign for \(\Delta S\) do you expect when the pressure on 0.600 mol of an ideal gas at \(350 \mathrm{~K}\) is increased isothermally from an initial pressure of 0.750 atm? (b) If the final pressure on the gas is 1.20 atm, calculate the entropy change for the process. (c) Do you need to specify the temperature to calculate the entropy change? Explain.

Consider the reaction $$ \mathrm{PbCO}_{3}(s) \rightleftharpoons \mathrm{PbO}(s)+\mathrm{CO}_{2}(g) $$ Using data in Appendix C, calculate the equilibrium pressure of \(\mathrm{CO}_{2}\) in the system at (a) \(400^{\circ} \mathrm{C}\) and (b) \(180^{\circ} \mathrm{C}\).

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