H 2 S ( g ) ⟶ H 2 ( g ) + S ( g ) H_2S(g)\longrightarrow H_2(g) + S(g) H 2 S ( g ) ⟶ H 2 ( g ) + S ( g )
here it is given as Kp =0.719 atm and p(H2 S)=.193 atm
so we will take x part of H2 S is change,
so we can write the equilibrium reaction as
H 2 S ( g ) ⟶ H 2 ( g ) + S ( g ) H_2S(g)\longrightarrow H_2(g) + S(g) H 2 S ( g ) ⟶ H 2 ( g ) + S ( g )
0.193 0 0
0.193-x x x
we can write for equilibrium constant Kp as
K p = P H 2 × P S P H 2 S K_p= \frac{P_{H_2}\times P_{S}}{P_{H_2S}} K p = P H 2 S P H 2 × P S
0.719 = x × x 0.193 − x 0.719= \frac{x\times x}{0.193-x} 0.719 = 0.193 − x x × x
0.139-0.719x = x 2 x=x^2 x = x 2
x 2 + 0.719 x − 0.139 = 0 x^2+0.719x-0.139=0 x 2 + 0.719 x − 0.139 = 0
using quadratic formula we can find
x = − 0.719 ± ( . 71 9 2 − ( 4 × 1 × ( − . 139 ) ) ) 2 x=\frac{-0.719 \pm\sqrt{(.719^2-(4\times1\times(-.139)))}}{2} x = 2 − 0.719 ± ( .71 9 2 − ( 4 × 1 × ( − .139 )))
x= − 0.719 + 1.04 2 = 0.1605 , x = − 0.719 − 1.04 2 = − 0.8795 \frac{-0.719+1.04}{2}=0.1605,x=\frac{-0.719-1.04}{2}=-0.8795 2 − 0.719 + 1.04 = 0.1605 , x = 2 − 0.719 − 1.04 = − 0.8795
so here , P H 2 = P S = 0.1605 a t m , a n d P H 2 S = 0.719 − 0.1605 = 0.5585 a t m P_{H_2}=P_S=0.1605 atm, and P_{H_2S}=0.719-0.1605=0.5585 atm P H 2 = P S = 0.1605 a t m , an d P H 2 S = 0.719 − 0.1605 = 0.5585 a t m
Here total pressure will be sum of all
PT = 0.1605+0.1605+0.5585=0.8795 atm
P T = 0.8795 a t m P_T= 0.8795 atm P T = 0.8795 a t m
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