Calculating Enthalpy Of Combustion Of Acetylene Using Hess's Law

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The enthalpy of combustion is a crucial thermochemical property, representing the heat released when one mole of a substance completely combusts in oxygen under standard conditions. This value is essential in various fields, including chemical engineering, where it's used for reactor design and energy balance calculations, and in environmental science, where it helps assess the energy potential of fuels and the impact of combustion processes. In this comprehensive guide, we will delve into the process of calculating the enthalpy of combustion for acetylene (C2H2C_2H_2), a highly versatile and widely used fuel in welding, cutting, and chemical synthesis. We will employ Hess's Law, a fundamental principle of thermochemistry, and standard enthalpies of formation to accurately determine the heat released during the combustion of acetylene. By understanding these principles and calculations, you will gain valuable insights into the energy transformations that occur during chemical reactions and their practical implications.

Acetylene (C2H2C_2H_2) holds significant importance across various industrial applications. Its high energy content and intense flame make it ideal for welding and cutting metals, where high temperatures are required. In chemical synthesis, acetylene serves as a crucial building block for producing a wide range of organic compounds, including plastics, synthetic rubber, and pharmaceuticals. Understanding the enthalpy of combustion of acetylene is paramount for optimizing these processes, ensuring efficiency, and maintaining safety. A precise determination of the heat released during combustion enables engineers to design equipment that can effectively manage the thermal output, preventing overheating and potential hazards. Furthermore, this knowledge is essential for accurately assessing the energy balance of chemical reactions involving acetylene, contributing to more sustainable and cost-effective industrial practices. In this article, we will explore the step-by-step method for calculating the enthalpy of combustion of acetylene, providing you with the tools and understanding necessary for real-world applications.

Understanding Enthalpy of Formation and Hess's Law

Before diving into the calculation, let's clarify two key concepts: enthalpy of formation and Hess's Law. The standard enthalpy of formation (Ξ”Hf∘\Delta H_f^\circ) is the change in enthalpy when one mole of a compound is formed from its constituent elements in their standard states (usually at 298 K and 1 atm). These values are often tabulated and readily available for many compounds, providing a crucial foundation for thermochemical calculations. For instance, the standard enthalpy of formation of carbon dioxide (CO2CO_2) represents the heat released or absorbed when one mole of CO2CO_2 is formed from solid carbon (graphite) and gaseous oxygen under standard conditions. Similarly, the standard enthalpy of formation of water (H2OH_2O) refers to the enthalpy change associated with the formation of one mole of liquid water from gaseous hydrogen and oxygen. Understanding these standard values is essential for applying Hess's Law effectively.

Hess's Law is a cornerstone of thermochemistry, stating that the enthalpy change for a chemical reaction is independent of the path taken between the initial and final states. In simpler terms, the total enthalpy change for a reaction is the same whether it occurs in one step or multiple steps. This principle allows us to calculate the enthalpy change of a reaction by summing the enthalpy changes of a series of reactions that add up to the overall reaction. Hess's Law is particularly useful when the direct measurement of the enthalpy change for a reaction is difficult or impossible. For example, the enthalpy change for the combustion of a complex organic compound can be calculated by breaking down the reaction into a series of simpler steps involving the formation and combustion of intermediate products. This indirect approach provides a practical and reliable method for determining the enthalpy change of reactions, making Hess's Law an indispensable tool in thermochemical calculations.

Given Information and the Combustion Reaction

We are given the balanced chemical equation for the combustion of acetylene:

2C2H2(g)+5O2(g)β†’4CO2(g)+2H2O(l)2 C_2 H_2 (g) + 5 O_2 (g) \rightarrow 4 CO_2 (g) + 2 H_2 O (l)

And we have a table of standard enthalpies of formation (Ξ”Hf∘\Delta H_f^\circ) for the compounds involved. Note that the physical states (gaseous or liquid) are crucial because they affect the enthalpy values. The table typically looks like this:

Compound Ξ”Hf∘\Delta H_f^\circ (kJ/mol)
C2H2(g)C_2 H_2 (g) +226.7
O2(g)O_2 (g) 0
CO2(g)CO_2 (g) -393.5
H2O(l)H_2 O (l) -285.8

Here, the standard enthalpy of formation for oxygen (O2O_2) is 0 kJ/mol because it is an element in its standard state. The positive value for acetylene indicates that its formation from carbon and hydrogen is an endothermic process, meaning it requires energy input. Conversely, the negative values for carbon dioxide and water indicate that their formation is exothermic, releasing energy. These values are critical for applying Hess's Law and calculating the overall enthalpy change for the combustion reaction. By understanding the standard enthalpies of formation for each compound, we can accurately determine the heat released or absorbed during the reaction, providing valuable insights into the energy transformations involved.

Applying Hess's Law to Calculate the Enthalpy of Combustion

According to Hess's Law, the enthalpy change for a reaction (Ξ”Hreaction∘\Delta H_{reaction}^\circ) can be calculated using the following equation:

Ξ”Hreaction∘=βˆ‘Ξ”Hf∘(products)βˆ’βˆ‘Ξ”Hf∘(reactants)\Delta H_{reaction}^\circ = \sum \Delta H_f^\circ (products) - \sum \Delta H_f^\circ (reactants)

This equation essentially states that the enthalpy change of a reaction is the difference between the sum of the standard enthalpies of formation of the products and the sum of the standard enthalpies of formation of the reactants. This method allows us to indirectly calculate the enthalpy change by using the known enthalpies of formation for each compound involved in the reaction. It is a powerful tool because it avoids the need for direct calorimetric measurements, which can be complex and time-consuming. Instead, we can rely on tabulated values and a simple calculation to determine the enthalpy change accurately.

For our reaction, we can expand this equation as follows:

Ξ”Hcombustion∘=[4Γ—Ξ”Hf∘(CO2)+2Γ—Ξ”Hf∘(H2O)]βˆ’[2Γ—Ξ”Hf∘(C2H2)+5Γ—Ξ”Hf∘(O2)]\Delta H_{combustion}^\circ = [4 \times \Delta H_f^\circ (CO_2) + 2 \times \Delta H_f^\circ (H_2O)] - [2 \times \Delta H_f^\circ (C_2H_2) + 5 \times \Delta H_f^\circ (O_2)]

Here, we multiply the standard enthalpy of formation of each compound by its stoichiometric coefficient from the balanced chemical equation. This is crucial because the enthalpy change is an extensive property, meaning it depends on the amount of substance involved. The stoichiometric coefficients ensure that the enthalpy changes are correctly scaled to the number of moles of each compound participating in the reaction. For example, if the balanced equation shows 2 moles of a product being formed, we must multiply its standard enthalpy of formation by 2 to account for the total enthalpy change associated with the formation of that amount of product. Similarly, we account for the reactants by subtracting their total enthalpy contributions from the total enthalpy of the products.

Plugging in the Values and Calculating

Now, let's substitute the given values into the equation:

Ξ”Hcombustion∘=[4Γ—(βˆ’393.5Β kJ/mol)+2Γ—(βˆ’285.8Β kJ/mol)]βˆ’[2Γ—(+226.7Β kJ/mol)+5Γ—(0Β kJ/mol)]\Delta H_{combustion}^\circ = [4 \times (-393.5 \text{ kJ/mol}) + 2 \times (-285.8 \text{ kJ/mol})] - [2 \times (+226.7 \text{ kJ/mol}) + 5 \times (0 \text{ kJ/mol})]

Perform the multiplications:

Ξ”Hcombustion∘=[βˆ’1574Β kJ/molβˆ’571.6Β kJ/mol]βˆ’[+453.4Β kJ/mol+0Β kJ/mol]\Delta H_{combustion}^\circ = [-1574 \text{ kJ/mol} - 571.6 \text{ kJ/mol}] - [+453.4 \text{ kJ/mol} + 0 \text{ kJ/mol}]

Add the values within the brackets:

Ξ”Hcombustion∘=βˆ’2145.6Β kJ/molβˆ’453.4Β kJ/mol\Delta H_{combustion}^\circ = -2145.6 \text{ kJ/mol} - 453.4 \text{ kJ/mol}

Finally, subtract to find the enthalpy of combustion:

Ξ”Hcombustion∘=βˆ’2599Β kJ/mol\Delta H_{combustion}^\circ = -2599 \text{ kJ/mol}

This calculation shows the total heat released when 2 moles of acetylene are combusted. However, the problem asks for the enthalpy of combustion for 1 mole of acetylene. Therefore, we need to divide the result by 2.

Calculating Enthalpy of Combustion per Mole

To find the enthalpy of combustion for 1 mole of acetylene, we divide the total enthalpy change by 2:

Ξ”Hcombustion(perΒ mole)∘=βˆ’2599Β kJ/mol2=βˆ’1299.5Β kJ/mol\Delta H_{combustion (per \text{ mole})}^\circ = \frac{-2599 \text{ kJ/mol}}{2} = -1299.5 \text{ kJ/mol}

Thus, the enthalpy of combustion of 1 mole of acetylene is approximately -1299.5 kJ/mol. This negative value indicates that the combustion of acetylene is an exothermic reaction, releasing a significant amount of heat. The high heat release is one of the reasons why acetylene is widely used in applications like welding and cutting, where high temperatures are required. Furthermore, this calculated value can be used for various practical applications, such as designing combustion systems, evaluating the energy content of acetylene fuel, and assessing the environmental impact of its combustion.

Conclusion: Significance of Enthalpy of Combustion

The enthalpy of combustion of acetylene, calculated to be approximately -1299.5 kJ/mol, is a critical value that underscores its utility as a high-energy fuel. This negative value signifies that the combustion of acetylene is a highly exothermic process, meaning it releases a substantial amount of heat into the surroundings. This characteristic is what makes acetylene ideal for applications such as welding and cutting metals, where intense heat is required to melt and fuse materials. The high heat output also contributes to its effectiveness in chemical synthesis, where it serves as a precursor for various industrial compounds.

The precise calculation of the enthalpy of combustion is not merely an academic exercise; it has significant practical implications. Understanding the energy released during combustion allows engineers and scientists to design and optimize combustion systems for maximum efficiency and safety. For example, in welding applications, knowing the enthalpy of combustion helps in selecting the appropriate fuel-to-oxygen ratio to achieve the desired flame temperature and cutting speed. In chemical reactors, the enthalpy of combustion is a crucial parameter for managing heat transfer and preventing thermal runaway, which can lead to hazardous conditions. Moreover, in the context of energy production, the enthalpy of combustion is used to evaluate the energy potential of fuels and to assess their environmental impact. A fuel with a high enthalpy of combustion can potentially deliver more energy per unit mass, but it is also essential to consider the emissions produced during combustion, such as carbon dioxide and other pollutants.

In summary, the ability to accurately calculate the enthalpy of combustion of compounds like acetylene is vital for a wide range of applications, from industrial processes to environmental assessments. By utilizing Hess's Law and standard enthalpies of formation, we can determine the heat released during combustion reactions, enabling us to make informed decisions about fuel selection, process design, and safety protocols. This thermochemical property provides a fundamental understanding of energy transformations in chemical reactions, contributing to safer, more efficient, and sustainable practices in various fields.