Calculations

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Calculations:

Initial standard:
−1
M (bet )=551.48 gmol
m(bet )=0.5130.0005 g % ∆ m=0.0975

m
n(bet )= % ∆ n=% ∆ m
M

0.513
n(bet )=
551.48
n(bet )=0.000930 9 ×10−7 mol % ∆ n=0.0975

n
c=
v
% ∆ c=% ∆ n+% ∆ v

v=0.5 0.0002l % ∆ v =0.04


0.000930
c= % ∆ c=0.0975+ 0.04
0.5
c=0.001863 × 10−6 mol l−1 % ∆ c=0.138

diluted standards:

vi
c f =c i % ∆ c f =% ∆ ci + % ∆ v i+ % ∆ v f
vf

0.002
c f (1)=0.00186 % ∆ c f =0.138+2.5+0.04
0.1
c f (1)=0.0000372± 1× 10−6 mol l−1 % ∆ c f =2.68

0.004
c f (2)=0.00186 % ∆ c f =0.138+1.25+0.04
0.1
c f (2)=0.0000744 ±1 ×10−6 mol l −1 % ∆ c f =1.428

0.006
c f (3)=0.00186 % ∆ c f =0.138+0.833+0.04
0.1
c f (3)=0.000112± 1× 10−6 mol l−1 % ∆ c f =1.01
0.008
c f (4 )=0.00186 % ∆ c f =0.138+0.625+0.04
0.1
c f (4 )=0.000149 ±1 ×10−6 mol l−1 % ∆ c f =0.803

0.01
c f (5)=0.00186 % ∆ c f =0.138+0.5+ 0.04
0.1
−6 −1
c f (5)=0.000186 ±1 ×10 mol l % ∆ c f =0.678
calculation of absorbance, concentration relationship.

Io
log 10 =l c
I
Io
log 10 = Absorbance=|¿|
I

using gradient of absorbance, concentration graph as ( l).


Additionally, adding the y intercept.

|¿|1257 c−0.01071
secondary standard:

m=0.983 0.0005 g % ∆ m=0.0699

m
n= % ∆ n=% ∆ m
M

0.983
n=
551.48
−6
n=0.00178 ±1 ×10 mol % ∆ n=0.0699

n
c= % ∆ c=% ∆ n+% ∆ v
v

v=0.5 ± 0.0002l % ∆ v =0.04


0.00178
c= % ∆ c=0.0699+ 0.04
0.5
−6
c=0.00357 ±2.99 ×10 mol l
−1
% ∆ c=0.1099

diluted secondary standard:

vi
c f =c i % ∆ c f =% ∆ ci + % ∆ v i+ % ∆ v f
vf

0.03
c=0.00357 % ∆ c f =0.1099+0.1+0.04
0.5
−7
c=0.000214 ± 4 ×10 mol l
−1
% ∆ c f =0.2199
Temperature vs concentration relationship:

Linear fit:

Each absorbance value is converted to a concentration using the


established relationship:

|¿|1257 c−0.01071

this give us the equation:

c=( −8.96 ×10−7 ) T +0.000247

considering the line of worst fit, we get the relationship:

∆ m=(−8.96 ×10 +6.81× 10 ) =2.15× 10


−7 −7 −7

−5
∆ ICPT =( 0.000247−0.000230 )=1.70 ×10

c=( −8.96 ×10 ± 2.15 ×10 ) T +0.000247 ±1.70 × 10


−7 −7 −5
Temperature vs concentration relationship revisited:

Arrhenius equation.
−E a

k = A e RT

where A is the Arrhenius constant, e is the mathematical value 2.72,


Ea is the activation energy of the reaction, R is the gas constant 8.314
JKmol-1 and T is the temperature in °C.

By combining the Arrhenius equation for the rate constant, k with the
1st order kinetics equation we get a very accurate relationship

( )
−Ea

− A e RT t
[ c ] =[c ]o e
substituting values, we get…
−226.3
T
−3.74 e
c=0.0002168 e

from this we can calculate further values

[c ]o=0.0002168

− At=−3.74
t=3 ×60=180 s
A=0.0208

−Ea
=−2263
R
−1
R=8.314 JK mol
−1
Ea =18814 J mol

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