Long chain branched EPDM compositions and processes for production thereof
Highly branched compositions including: (i) from about 96 wt % to about 99.9 wt % metallocene catalyzed ethylene propylene diene derived units; and (ii) from about 0.1 wt % to about 4 wt % multifunctional monomer derived units, wherein the highly branched composition has: (a) a Mooney viscosity ML (1+4) at 125° C. of about 30 to 100 MU, (b) a Mooney relaxation area MLRA of about 100 to about 1000, (c) a branching index, g′(vis) of less than about 0.9, (d) a phase angle, δ, of less than about 55 degrees at a complex modulus of 10 kPa, measured at 190° C., and (e) a degree of shear thinning greater than about 0.95, measured at 190° C., are disclosed herein. Homogeneous blends including this composition are also described. Processes to make the highly branched composition and the homogeneous blend are also described herein.
1. A process for producing a highly branched composition comprising:
(i) contacting:
(a) from about 96 wt % to about 99.9 wt % of at least one metallocene catalyzed ethylene propylene diene rubber, based on the total weight of the rubber and multifunctional monomers;
(b) from about 0.1 to about 4 wt % of at least one multifunctional monomer, based on the total weight of the rubber and multifunctional monomers;
(c) at least one free radical generator; and
(ii) obtaining a highly branched composition.
2. The process of claim 1 , wherein the highly branched composition has one or more of the following properties:
(a) a Mooney viscosity ML (1+4) at 125° C. of about 30 to 100 MU;
(b) a Mooney relaxation area MLRA of about 100 to about 1000;
(c) a branching index, g′(vis) of less than about 0.9;
(d) a phase angle, δ, of less than about 55 degrees at a complex modulus of 10 kPa, measured at 190° C.; and
(e) a degree of shear thinning greater than about 0.95, measured at 190° C.
3. The process of claim 1 , wherein from about 0.1 wt % to about 3.5 wt % of the free radical generator is used in the contacting step, based on the total weight of the rubber and multifunctional monomers.
4. The process of claim 1 , wherein the multifunctional monomer comprises one or more of vinyl compounds, allylic compounds, acrylate compounds, and combinations thereof.
5. The process of claim 1 , wherein the multifunctional monomer is selected from the group consisting of 3,9-divinyl-2,4,8,10-tetraoxaspiro[5,5]undecane, 2,5-norbornadiene, divinylphenylphosphine, divinyl sulfone, divinyl sulfoxide, 1-3-divinyltetramethyldisiloxane, 1,2 polybutadiene, divinyl benzene, and combinations thereof.
6. The process of claim 1 , wherein the multifunctional monomer is selected from the group consisting of triallyl trimesate, triallyl trimellitate, diallyl terephthalate, diallyl isophthalate, diallyl phthalate, triallylcyanurate, triallylisocyanurate, triallylamine, triallyl 1,3,5-benzenetricarboxylate, triallylphosphine, triallyl phosphate, 1,3,5-triallyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione, and combinations thereof.
7. The process of claim 1 , wherein the multifunctional monomer is selected from the group consisting of trimethylolpropane trimethacrylate, trimethylolpropane triacrylate, polyethylene glycol dimethacrylate, ethylene glycol dimethacrylate, triethylene glycol diacrylate, pentaerythritol triacrylate, pentaerythrithyl tetramethacrylate 1,4-butanediol diacrylate, 1,6-hexanediol diacrylate, and combinations thereof.
8. The process of claim 1 , wherein from about 98 wt % to about 99.9 wt % ethylene propylene diene rubber is used in the contacting step, based on the total weight of the rubber and multifunctional monomers.
9. The process of claim 1 , wherein from about 0.5 wt % to about 2 wt % multifunctional monomer is used in the contacting step, based on the total weight of the rubber and multifunctional monomers.
10. The process of claim 1 , wherein the free radical generator comprises one or more of benzoyl peroxide, methyl ethyl ketone peroxide, tert-butyl peroxy benzoate, tert-butyl perbenzoate, tert-butylperoxy acetate, tert-butyl (2-ethylhexyl) monoperoxy carbonate, n-butyl-4,4-di-(tert-butyl peroxy) valerate, 1,1-bis(tert-butylperoxy)cyclohexane, 1,1-bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane, 2,2-bis(tert-butylperoxy)butane, tert-butylcumylperoxide, bis-(tert-butylperoxy isopropyl)benzene, di-tert-butylperoxide, 2,5-dimethyl-2,5-di(tert-butylperoxy)hexane, cyclohexanone peroxide, t-butylperoxyisopropyl carbonate, di-ti-butyl terphthalate, 2,5-dimethyl-2,5-di(t-butylperoxy)hexene, 2,5-dimethyl-2,5-di(t-butylperoxy) hexyne-3, di-(tert-amyl) peroxide, bis(alpha-methylbenzyl) peroxide, benzoyl peroxide, 3,6,9-triethyl-3,6,9-trimethyl-1,4,7-triperoxonane, bis(tert-butylperoxy)-diisopropylbenzene, di-tert-butyl peroxide, cumene hydroperoxide, tert-butyl hydroperoxide, hydroperoxides, dilauryl peroxide, dicumyl peroxide, derivatives thereof, or combinations thereof.
11. The process of claim 1 , wherein the metallocene catalyzed ethylene propylene diene rubber comprises at least 35 wt % ethylene, based on the total weight of the metallocene catalyzed ethylene propylene diene rubber.
12. The process of claim 1 , wherein the metallocene catalyzed ethylene propylene diene rubber comprises at least 2 wt % ethylidenenorbornene, based on the total weight of the metallocene catalyzed ethylene propylene diene rubber.
13. The process of claim 1 , further comprising drying the highly branched composition to remove residual free radical generator.