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A quantity of gas occupies 0.2m³ at a pressure of 1000kN/m² and a temperature of 348°C. it is first heated at constant volume until the pressure reaches 4MPa. It is then expanded adiabatically until the pressure reaches is 280kPa. Gamma for the gas is 1.41 and R=0.228 kJ/kgK. Calculate:

Physics

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Answers

3 parts
1.1

621.15 K\text{621.15 K}

1266.2 K\text{1266.2 K}

1.2

1463.0 kJ\text{1463.0 kJ}

1.3

956.4 kJ\text{956.4 kJ}

Step-by-step solution

7 steps

Here's the solution to Question 1:

Given data:

  • Initial volume, V1=0.2 m3V_1 = 0.2 \, \text{m}^3
  • Initial pressure, P1=1000 kN/m2=1000 kPaP_1 = 1000 \, \text{kN/m}^2 = 1000 \, \text{kPa}
  • Initial temperature, T1=348∘C=348+273.15=621.15 KT_1 = 348^\circ\text{C} = 348 + 273.15 = 621.15 \, \text{K}
  • Process 1-2 (Constant volume heating):
    • Pressure after heating, P2=4 MPa=4000 kPaP_2 = 4 \, \text{MPa} = 4000 \, \text{kPa}
    • Volume V2=V1=0.2 m3V_2 = V_1 = 0.2 \, \text{m}^3
  • Process 2-3 (Adiabatic expansion):
    • Final pressure, P3=280 kPaP_3 = 280 \, \text{kPa}
  • Adiabatic index, γ=1.41\gamma = 1.41
  • Characteristic gas constant, R=0.228 kJ/kgKR = 0.228 \, \text{kJ/kgK}

Part 1.1· 3 steps

The temperature at the beginning and at the end of expansion

  1. Determine the temperature at the beginning of the process (T1T_1).

    The initial temperature is given:

    T1=348∘C=348+273.15=621.15 KT_1 = 348^\circ\text{C} = 348 + 273.15 = 621.15 \, \text{K}
  2. Determine the temperature at the beginning of expansion (T2T_2).

    Process 1-2 is a constant volume process (V1=V2V_1 = V_2). For an ideal gas, the relationship between pressure and temperature at constant volume is:

    P1T1=P2T2\frac{P_1}{T_1} = \frac{P_2}{T_2}

    Rearrange to solve for T2T_2:

    T2=T1(P2P1)T_2 = T_1 \left(\frac{P_2}{P_1}\right)

    Substitute the values:

    T2=621.15 K×(4000 kPa1000 kPa)T_2 = 621.15 \, \text{K} \times \left(\frac{4000 \, \text{kPa}}{1000 \, \text{kPa}}\right) T2=621.15 K×4=2484.6 KT_2 = 621.15 \, \text{K} \times 4 = 2484.6 \, \text{K}
  3. Determine the temperature at the end of expansion (T3T_3).

    Process 2-3 is an adiabatic expansion. For an adiabatic process, the relationship between temperature and pressure is:

    T2P2(1−γ)/γ=T3P3(1−γ)/γT_2 P_2^{(1-\gamma)/\gamma} = T_3 P_3^{(1-\gamma)/\gamma}

    Rearrange to solve for T3T_3:

    T3=T2(P3P2)(γ−1)/γT_3 = T_2 \left(\frac{P_3}{P_2}\right)^{(\gamma-1)/\gamma}

    Substitute the values:

    T3=2484.6 K×(280 kPa4000 kPa)(1.41−1)/1.41T_3 = 2484.6 \, \text{K} \times \left(\frac{280 \, \text{kPa}}{4000 \, \text{kPa}}\right)^{(1.41-1)/1.41} T3=2484.6 K×(0.07)0.41/1.41T_3 = 2484.6 \, \text{K} \times \left(0.07\right)^{0.41/1.41} T3=2484.6 K×(0.07)0.29078T_3 = 2484.6 \, \text{K} \times \left(0.07\right)^{0.29078} T3=2484.6 K×0.5096T_3 = 2484.6 \, \text{K} \times 0.5096 T3≈1266.2 KT_3 \approx 1266.2 \, \text{K}

    The temperature at the beginning of the process is 621.15 K\boxed{\text{621.15 K}}.
    The temperature at the end of expansion is 1266.2 K\boxed{\text{1266.2 K}}.

Part 1.2

1463.0 kJ\text{1463.0 kJ}

The heat energy supplied.

  1. Calculate the mass of the gas (mm).

    Use the ideal gas law for state 1: P1V1=mRT1P_1 V_1 = m R T_1.

    m=P1V1RT1m = \frac{P_1 V_1}{R T_1}

    Substitute the values:

    m=1000 kPa×0.2 m30.228 kJ/kgK×621.15 Km = \frac{1000 \, \text{kPa} \times 0.2 \, \text{m}^3}{0.228 \, \text{kJ/kgK} \times 621.15 \, \text{K}} m=200141.6222 kgm = \frac{200}{141.6222} \, \text{kg} m≈1.4122 kgm \approx 1.4122 \, \text{kg}
  2. Calculate the specific heat capacity at constant volume (CvC_v).

    The relationship between CvC_v, RR, and γ\gamma is Cv=Rγ−1C_v = \frac{R}{\gamma - 1}.

    Cv=0.228 kJ/kgK1.41−1C_v = \frac{0.228 \, \text{kJ/kgK}}{1.41 - 1} Cv=0.2280.41 kJ/kgKC_v = \frac{0.228}{0.41} \, \text{kJ/kgK} Cv≈0.5561 kJ/kgKC_v \approx 0.5561 \, \text{kJ/kgK}
  3. Calculate the heat energy supplied (Q1−2Q_{1-2}).

    For a constant volume process, the heat supplied is equal to the change in internal energy:

    Q1−2=mCv(T2−T1)Q_{1-2} = m C_v (T_2 - T_1)

    Substitute the values:

    Q1−2=1.4122 kg×0.5561 kJ/kgK×(2484.6 K−621.15 K)Q_{1-2} = 1.4122 \, \text{kg} \times 0.5561 \, \text{kJ/kgK} \times (2484.6 \, \text{K} - 621.15 \, \text{K}) Q1−2=1.4122×0.5561×1863.45 kJQ_{1-2} = 1.4122 \times 0.5561 \times 1863.45 \, \text{kJ} Q1−2≈1463.0 kJQ_{1-2} \approx 1463.0 \, \text{kJ}

    The heat energy supplied is 1463.0 kJ\boxed{\text{1463.0 kJ}}.

Part 1.3

956.4 kJ\text{956.4 kJ}

The work energy transferred.

  1. Calculate the work done during the adiabatic expansion (W2−3W_{2-3}).

    For an adiabatic process, the work done by the gas is given by:

    W2−3=mCv(T2−T3)W_{2-3} = m C_v (T_2 - T_3)

    Substitute the values:

    W2−3=1.4122 kg×0.5561 kJ/kgK×(2484.6 K−1266.2 K)W_{2-3} = 1.4122 \, \text{kg} \times 0.5561 \, \text{kJ/kgK} \times (2484.6 \, \text{K} - 1266.2 \, \text{K}) W2−3=1.4122×0.5561×1218.4 kJW_{2-3} = 1.4122 \times 0.5561 \times 1218.4 \, \text{kJ} W2−3≈956.4 kJW_{2-3} \approx 956.4 \, \text{kJ}

    The work energy transferred is 956.4 kJ\boxed{\text{956.4 kJ}}.

Part 1.4

State Joules law.

Joule's law states that the internal energy of an ideal gas depends only on its temperature, not on its pressure or volume. This means that for an ideal gas, the change in internal energy is zero during an isothermal process.

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