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Radical copolymerization

Radical copolymerization. Regular copolymer. Random copolymer. Block copolymer. Graft copolymer. Actual copolymer (case). Chap 11. Free Radical Copolymerization. Copolymer Equation. Only Binary Case Two Monomers; M1 + M2. Steady State Assumption.

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Radical copolymerization

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  1. Radical copolymerization Regular copolymer Random copolymer Block copolymer Graft copolymer Actual copolymer (case) Chap 11. Free Radical Copolymerization

  2. Copolymer Equation Only Binary Case Two Monomers; M1 + M2 Steady State Assumption and chain transfer & termination compared w/ propagation ……①

  3. Copolymer Equation ……② Instantaneous ratio of monomers in copolymer From ① and ② monomer reactivity ratio where , Copolymer Eq.

  4. Meaning of r & Definition of f1, F1 Meaning of r characterizes the reactivity of the 1 radical with respect to the two monomers, 1 and 2 then homopolymerization growth is preferred then only reaction with 2 will occur Define f1, F1 f1, f2 : mole fractions of monomers in feed F1, F2 : mole fractions of monomers in polymer …… ③ ……④ ……⑤ From ③, ④ How come?

  5. Ideal Copolymerization Ideal Copolymerization where Most ionic copolymerizations are characterizes by the ideal type of behavior When , the two monomers show equal reactivity toward both propagating species random copolymer

  6. Ideal Copolymerization or One of the monomer us nire reactive than The other toward both propagating spices. The copolymer will contain a larger proportion of the more reactive monomer in random placement 1 F1 1 0 f1 Surfing to the internet For further details about Ideal Copolymerization Click next homepage. http://www.chem.rochester.edu/~chem421/copoly.htm

  7. Alternating Copolymerization Alternating Copolymerization 1 or Cross-over point 0 1 As r1, r2 approach to zero, alternating tendency can be observed If → perfect alternation! If plots cross the line representing , If , then, become a homopolymer

  8. Alternating Copolymerization Mean of Cross-over Point At these crossover points the copolymer and feed compositions are the same and copolymerization occurs without a change in the feed composition Such copolymerizaions are termed Azeotropic copolymeriztions. Condition of Azeotropic copolymeriztion and ∵

  9. Alternating Copolymerization ∴

  10. Alternating Copolymerization ( and ) Both types of propagating species preferentially add monomer M1. there is a tendency toward consecutive Homopolymerization of the two monomers. And then monomer M2 will subsequently homopolymerize. In the result r1r2=1 ideal or random fix r2=0.5 Addition monimer A and A* Can not prepare copolymer It’s alternating up to 0.5, and above 0.5 there’s no formation of copolymer

  11. Alternating Copolymerization r2=0.5 azeotropic comp alternating r2=0.5 r1=1 no azeotrope r1, r2 > 1 Case tend to be a block copolymerization

  12. Alternating Copolymerization Drift: r1, r2 > 1 block azeotrope r1, r2 <1 alternating Block COPOLYMERIZATION finally , HW #6. Solve S.S. expression for a monomer concentration and substitute into the original composition equation which contains the active center. You can get eq. in terms of active center concentrations and if necessary define new kind of new reactivity ratio in eq.

  13. Experimental Determination of r1 & r2 Experimental Determination of r1 & r2 • Mayo and Lewis rearrange copolymer eq. and can get copolymer comp. monomer comp     then vary r1 value (put) and iterate

  14. Experimental Determination of r1 & r2 2. Finemann and Ross Recall A const. B const. at low conversion Slope : r1 Intersection : r2

  15. Relationship Between ξand F1, f1 Relationship Between ξ and F1, f1 Material Balance for M1 where [M] = total # of moles of monomers decrease of M1 monomer

  16. Effect of Reaction Condition Reaction medium Depend on Solubility, PH, Viscosity, and Polarity Temperature But the effect of temperature on r is not large Pressure But the effect of pressure on r is not large Reactivity Next page

  17. Effect of Reaction Condition Structure and Reactivity I. Resonance Stabilization II. Polar Effects III. Steric Effects • I.Resonance Stabilization * Walling’s “Free Radicals in Solution”

  18. Structure and Reactivity Define rA, rB : monomer reactivity ratios RA, RB : active center reactivity ratios

  19. Structure and Reactivity TABLE I. Propagation Rate Constants, Monomer Reactivity Ratios, and Active Center Reactivity Ratios for Radical Chain-Growth Polymerizations1 1All values are based on data collected at 60℃ 2AN=acrylonitrile; MA=methylacrylate; MMA=methylmetacrylate; STY=styrene; VA=vinyl acetate

  20. Structure and Reactivity Active Center Reactivity Ratios vs. Monomer Reactivity Ratios when then when The effect in relative reactivity of the active center is more stronger than that of monomer. The monomer reactivity gets affect in opposite way comparing to the active center reactivity.

  21. Structure and Reactivity Odian Table 6-3. Relative Reactivities(1/r) of Monomers

  22. Structure and Reactivity @ Substituent Effects Φ, CH2=CH- > -C≡N, -COR > -COOH, -COOR > -Cl > -O-COR, -R > -OR, -H monomers increase relative reactivity by resonance stabilization. The resonance stability of the monomer increases the reactivity of the monomer. The resonancestability of the radical is weakened reactivity of the radical. Table 6-4 Rate Constant(k12) for Radical-Monomer Reactions

  23. Structure and Reactivity Resonance stabilization of Active Center Transition State Theory AB* Activated complex ΔER A + B P.E. compound ΔHR Increasing Separation of A & B

  24. Structure and Reactivity AB Morse curve P.E. A+B repulsion curve Increasing Separation of A & B ΔE1‡ > ΔE3‡ then Rxn III is less stable than Rxn I ΔHR3‡ < ΔHR1‡ R  P.E. R + M Reaction I R  ΔE1‡ Reaction III R  ΔE3‡ Rs  + M Increasing Separation of Reactant

  25. Structure and Reactivity Resonance stability of Active Center becomes primary Resonance stability ofMonomer becomes secondary

  26. Structure and Reactivity |-ΔH | ① > ② > ③ > ④ ΔE‡ ④ > ③ > ② > ① Surfing to the internet For further details about Free Radical Polymerization Click the link below. http://www.chem.rochester.edu/~chem421/frfull.htm

  27. Structure and Reactivity II. Polar Effects Tend to cause alternation in a copolymerization i.e. for polar effects e : tendency to give monomer a polar effects Alfrey-Price Q,e scheme (Polarity Values)

  28. Structure and Reactivity @ Q-e scheme of Alfred Price forecast randomness of copolymerization , As know r, prediction is possible to polar, resonance effect Guidance to chemists where P : active center reactivity Q : monomer reactivity i, j : active center, monomer, respectively

  29. Structure and Reactivity So that, this equation forecasts Base materials use styrene : (arbitrary) fair results, but not absolute in predicting r using Q-e scheme. alternating tendency is correct

  30. Structure and Reactivity Active Center Reacting Ratios P-e scheme

  31. Structure and Reactivity The criticism againstQ-e scheme Reference state arbitrarily set. Alternating effect was observed due to fixed charges not due to the induced dipole Exercise) How to indicate Randomness of Copolymer with Q-e scheme ? We can forecast alternation or randomness through Q-e scheme, however, why can not forecast Blockcopolymerization? (algebraic standpoint) Surfing to the internet For further details about Free Radical Polymerization Click the link below http://www.kcpc.usyd.edu.au/resources/notes/gilbertnotes3.pdf

  32. Structure and Reactivity III. Steric Effects 1) 1,2-disubstituted ethylene do not homopolymerize readily 2) 1,1-disubstituted ethylene II. Polar Effects planar conformation tetrahedral conformation more reactive

  33. Structure and Reactivity 3) Cis-trans Effect The trans is stabilized the cis than thermodynamics(Heat of Hydrogenation) Planarity! Easier for trans than cis Steric Effect! Surfing to the internet For further details about Free Radical Polymerization Click the link below. http://pslc.ws/macrog/lab/unit1.htm

  34. Structure and Reactivity Table 6-5 Rate Constants( ) for Radical-Monomer Reactionsa a Values were calculated from data in Table 3-11 and 6-2 and [66] 1,1-disubs. High reactive Mono subs. Tri subs. Trans 1,2 Cis 1,2

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