Mayo-Lewis equation


Mayo-Lewis equation

The Mayo-Lewis equation or copolymer equation in polymer chemistry describes the distribution of monomers in a copolymer ["Copolymerization. I. A Basis for Comparing the Behavior of Monomers in Copolymerization; The Copolymerization of Styrene and Methyl Methacrylate" Frank R. Mayo and Frederick M. Lewis J. Am. Chem. Soc.; 1944; 66(9) pp 1594 - 1601; DOI|10.1021/ja01237a052] :

Taking into consideration a monomer mix of two components M_1, and M_2, and the four different reactions that can take place at the reactive chain end terminating in either monomer (M^*,) with their reaction rate constants k,:

:M_1^* + M_1 xrightarrow{k_{11 M_1M_1^* ,:M_1^* + M_2 xrightarrow{k_{12 M_1M_2^* ,:M_2^* + M_1 xrightarrow{k_{21 M_2M_1^* ,:M_2^* + M_2 xrightarrow{k_{22 M_2M_2^* ,

and with reactivity ratio's defined as:

:r_1 = frac{k_{11{k_{12 ,:r_2 = frac{k_{22{k_{21 ,

the copolymer equation is given as:

:frac {dleft [M_1 ight] }{dleft [M_2 ight] }=frac{left [M_1 ight] left (r_1left [M_1 ight] +left [M_2 ight] ight)}{left [M_2 ight] left (left [M_1 ight] +r_2left [M_2 ight] ight)}

with the concentration of the components given in square brackets. The equation gives the copolymer composition at any instant during the polymerization.

Limiting cases

From this equation several limiting cases can be derived:
* r_1 = r_2 >> 1 , with both reactivity ratios very high the two monomers have no inclination to react to each other except with themselves leading to a mixture of two homopolymers.
* r_1 = r_2 > 1 , with both ratio's larger than 1, homopolymerization of component M_1 is favored but in the event of a crosspolymerization by M_2 the chain-end will continue as such giving rise to block copolymer
* r_1 = r_2 approx 1 , with both ratio's around 1, monomer 1 will react as fast with another monomer 1 or monomer 2 and a random copolymer results.
* r_1 = r_2 approx 0 , with both values approaching 0 the monomers are unable to react in homopolymerization and the result is an alternating polymer
* r_1 >> 1 >> r_2 , In the initial stage of the copolymerization monomer 1 is incorporated faster and the copolymer is rich in monomer 1. When this monomer gets depleted, more monomer 2 segments are added. This is called composition drift.

An example is maleic anhydride and stilbene, with reactivity ratio:
* Maleic anhydride (r_1, = 0.08) & cis-stilbene ( r_2 , = 0.07)
* Maleic anhydride ((r_1, = 0.03) & trans-stilbene ( r_2 , = 0.03)

Both of these compounds do not homopolymerize and instead, they react together to give exclusively alternating copolymer.

Another form of the equation is:

F_1=1-F_2=frac{r_1 f_1^2+f_1 f_2}{r_1 f_1^2+2f_1 f_2+r_2f_2^2},

where F, stands the mole fraction of each monomer in the copolymer:

F_1 = 1 - F_2 = frac{d M_1}{d (M_1 + M_2)} ,

and f, the mole fraction of each monomer in the feed:

f_1 = 1 - f_2 = frac{M_1}{(M_1 + M_2)} ,

When the copolymer composition has the same composition as the feed, this composition is called the "azeotrope".

Calculation of reactivity ratios

The reactivity ratio's can be obtained by rewriting the copolymer equation to:

frac{f(1-F)}{F} = r_2 - r_1left(frac{f^2}{F} ight) ,

with

f = frac{ [M_1] }{ [M_2] } , in the feed

and

F = frac{d [M_1] }{d [M_2] } , in the copolymer

A number of copolymerization experiments are conducted with varying monomer ratio's and the copolymer composition is analysed at low conversion. A plot of frac{f(1-F)}{F}, versus frac{f^2}{F}, gives a straight line with slope r_1, and intercept r_2,.

A semi-empirical method for the determination of reactivity ratio's is called the Q-e scheme.

Equation derivation

Monomer 1 is consumed with reaction rate ["Introduction to polymers" R.J. Young ISBN 0412221705] :

frac{-d [M_1] }{dt} = k_{11} [M_1] sum [M_1^*] + k_{21} [M_1] sum [M_2^*] ,

with sum [M_x^*] the concentration of all the active centers terminating in monomer 1 or 2.

Likewise the rate of disappearance for monomer 2 is:

frac{-d [M_2] }{dt} = k_{22} [M_2] sum [M_2^*] + k_{21} [M_2] sum [M_1^*] ,

Division of both equations yields:

frac{d [M_1] }{d [M_2] } = frac{ [M_1] }{ [M_2] } left( frac{k_{11}frac{sum [M_1^*] }{sum [M_2^*] } + k_{21 {k_{12}frac{sum [M_2^*] }{sum [M_2^*] } + k_{22 ight) ,

The ratio of active center concentrations can be found assuming steady state with:

frac{dsum [M_1^*] }{dt} = frac{dsum [M_2^*] }{dt} approx 0,

meaning that the concentration of active centres remains constant, the rate of formation for active center of monomer 1 is equal to the rate of their destruction or:

k_{21} [M_1] sum [M_2^*] = k_{12} [M_2] sum [M_1^*] ,

or

frac{sum [M_1^*] }{sum [M_2^*] } = frac{k_{21} [M_1] }{k_{12} [M_2] },

External links

* copolymer equation applet @eng.utah.edu [http://www.eng.utah.edu/~nairn/applets/Copoly.html Link]
* copolymers @zeus.plmsc.psu.edu [http://zeus.plmsc.psu.edu/~manias/MatSE443/chapter5.pdf Link]

References


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