Molten steel at 1900 K having dissolved hydrogen needs to be vacuum degassed. The equilibrium partial pressure of hydrogen to be maintained to achieve 1 ppm (mass basis) of dissolved hydrogen is ......... Torr (rounded off to two decimal places). Given: For the hydrogen dissolution reaction in molten steel \( \left( \frac{1}{2} {H}_2(g) = [{H}] \right) \), the equilibrium constant (expressed in terms of ppm of dissolved H) is: \[ \log_{10} K_{eq} = \frac{1900}{T} + 2.4 \] 1 atm = 760 Torr.
We need to find the equilibrium partial pressure of hydrogen at 1900 K.
Step 1: Calculate \( K_{eq} \) at 1900 K Substituting \( T = 1900 \): \[ \log_{10} K_{eq} = \frac{1900}{1900} + 2.4 = 1 + 2.4 = 3.4 \] \[ K_{eq} = 10^{3.4} = 2511.88 \] Step 2: Use the equilibrium constant to calculate the partial pressure of hydrogen The equilibrium constant for the hydrogen dissolution reaction is: \[ K_{eq} = \frac{P_{{H}_2}}{[{H}]^2} \] Since 1 ppm corresponds to \( [{H}] = 10^{-6} \) (ppm is a mass basis, but we will assume concentration is proportional), we have: \[ P_{{H}_2} = K_{eq} \times [{H}]^2 = 2511.88 \times 10^{-6} = 0.0025 \, {Torr} \]
Consider the gas phase reaction: \[ CO + \frac{1}{2} O_2 \rightleftharpoons CO_2 \] At equilibrium for a particular temperature, the partial pressures of \( CO \), \( O_2 \), and \( CO_2 \) are found to be \( 10^{-6} \, {atm} \), \( 10^{-6} \, {atm} \), and \( 16 \, {atm} \), respectively. The equilibrium constant for the reaction is ......... \( \times 10^{10} \) (rounded off to one decimal place).
Consider the following reactions and their standard Gibbs free energies (in J): \[ {Fe(s)} + \frac{1}{2} {O}_2(g) \rightleftharpoons {FeO(s)} \quad \Delta G^\circ = -264900 + 65T \] \[ 2 {H}_2(g) + {O}_2(g) \rightleftharpoons 2 {H}_2{O(g)} \quad \Delta G^\circ = -492900 + 109T \] Assuming Fe and FeO to be pure and no solubility of gases in the solids, the value of \( \frac{p_{H_2O}}{p_{H_2}} \) required to reduce solid FeO to solid Fe at 1000 K is _________ (rounded off to two decimal places). Given: Ideal gas constant \( R = 8.314 \, {J mol}^{-1} {K}^{-1} \).
The reaction represented by \( A \rightarrow B \) follows first-order kinetics. At a given temperature, 20% of the reaction is completed in 223 s. The time taken to complete 50% of the reaction at the same temperature is _________ s (rounded off to the nearest integer).
Match the phenomena in Column I with the typical observations in Column II.
Radiative heat flux \( \dot{q} \) at a hot surface at a temperature \( T_s \) can be expressed as \[ \dot{q} = A f(T_s, T_\infty) (T_s - T_\infty) \] where \( A \) is a constant and \( T_\infty \) is the temperature of the surroundings (temperatures are expressed in K). The function \( f(T_s, T_\infty) \) is given by ______.
Match the steel plant related processes in Column I with the associated information in Column II.
Consider the phase diagram of a one-component system given below. \( V_{\alpha} \), \( V_{\beta} \), and \( V_{{Liquid}} \) are the molar volumes of \( \alpha \), \( \beta \), and liquid phases, respectively. Which one of the following statements is TRUE? Given: The change in molar enthalpies, \( \Delta H_{\alpha \to \beta} \) and \( \Delta H_{\beta \to {Liquid}} \), are positive.
For two continuous functions \( M(x, y) \) and \( N(x, y) \), the relation \( M dx + N dy = 0 \) describes an exact differential equation if