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aalyn [17]
2 years ago
14

Consider the air over a city to be a box 100km on a side that reaches up to an altitude of 1.0 km. Clean air is blowing into the

box along one of its sides with a speed of 4 m/s. Suppose an air pollutant with a reaction rate k=0.20/hr is emitted into the box at a total rate of 10.0kg/s. Find the steady-state concentration if the air is assumed to be completely mixed.
Chemistry
1 answer:
Mariana [72]2 years ago
4 0

Explanation:

It is known that equation for steady state concentration is as follows.

            C_{a} = \frac{QC}{Q + kV}

where,   Q = flow rate

              k = rate constant

              V = volume

              C = concentration of the entering air

Formula for volume of the box is as follows.

                 V = a^{2}h

                    = 100 \times 100 \times 1

                    = 10000 km^{3}

Now, expression to determine the discharge is as follows.

                  Q = Av

                      = 100 \times 1 \times \frac{4 m}{s} \times \frac{km}{1000 m}

                      = 0.4 km^{3}/s

And,    m (loading) = 10kg/s,

           k = 0.20/hr

as   1 km^3 = 10^{12} L (if u want kg/L as concentration)

Now, calculate the concentration present inside as follows.

     C_{in} = \frac{10kg/s}{0.4 km^3/s}

                 = 25 kg/km^3

Now, we will calculate the concentration present outwards as follows.

       C_{out} = {C_{in}}{(1 + k \times t)},

and,      t = \frac{V}{Q}

               = 25000 s or 6.94 hr

Hence,   C_{out} = \frac{25}{(1 + 0.20 \times 6.94)}

                         = 10.47 kg/km^3

Thus, we can conclude that the the steady-state concentration if the air is assumed to be completely mixed is C_{out} = 10.47 kg/km^3 and C_{in} = 25 kg/km^3 .

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Answer:

618 J/Kmol

T > 1.36 x 10³ K

Explanation:

The  balanced reaction of interest is:

                           SO₃ (g) + SCl₂ (l) ⇒    SOCl₂ (l) +     SO₂ (g)

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ΔHºf (kJ/mol)      -396          -50.0          -245.6         -296.8

Sº(J/mol·K)             256.7       184               ?               -248.1

ΔGº=  -75.2 kJ

We know, we can find the standard  change inGibb´s free energy from the equation:

ΔGºrxn =  ΔHºrxn - TΔSºrxn

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ΔHºrxn = ( -245.6 + (-296.8) ) - ( -396 - 50) kJ = - 96.4 kJ

Similarly  for ΔSºrxn

 ΔSºrxn = (-0.248.1 +Sº SOCl₂) - (0.256.7 +0.184) kJ/K

= -0.689 kJ /K -+ Sº SOCl₂

Plugging the values for the expression for  ΔGºrxn:

-75.2 kJ = -96.4 kJ - 298 K  x  ( -0.689 kJ /K + Sº SCl₂ )

-75.2 kJ = -96.4 kJ + 205.3 Kj - 298 Sº SCl₂

-184  kJ = -298 K  x Sº SCl₂

0.618 kJ/molK = Sº SCl₂

= 0.618 kJ/K x 1000 J = 618 J/Kmol

For the second part we will still be using the Gibb´s free energy change  equation as above , but now we will solve for T when the reaction becomes  non-spontaneous.

For the reaction to become non-spontaneous  ΔGº is positive, and this happens when the term  TΔSº becomes greater tha ΔHº:

ΔGºrxn =  ΔHºrxn - TΔSºrxn

0 =   ΔHºrxn - TΔSºrxn ⇒  TΔSºrxn  =  ΔHºrxn

                                           T= ΔHºrxn / ΔSºrxn

ΔSºrxn  = -0.689 J/Kmol + 0.618 J/Kmol = -0.0710 kJ/Kmol

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T =  - 96.4 kJ / -0.071 kJ/K = 1.36 x 10³ K

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