Process for the treatment of linear low density polyethylene by organic peroxides which generate free radicals

Abstract

The invention relates to a process of thermomechanical treatment in the molten state, in the presence of organic peroxides, of co-polymers with a density less than 0.935, obtained by co-polymerization under a pressure of less than 4 MP a of ethylene and a higher alpha-olefin. The co-polymers thus treated may advantageously be used for the manufacture of finished objects such as films according to the current techniques of conversion of "high pressure" type polyethylene.

We claim: 
     
       1. A process for treating co-polymers of linear low density polyethylene having a density of less than 0.935, a fluidity index at 190° C. under 2.16 kg as per NFT 51016 standard, Method A, of between 0.3 and 50, and a branching index greater than 0.95, in which the co-polymer is obtained by .Iadd.a gaseous phase .Iaddend.copolymerization under a pressure less than 4 MP a , of a mixture of ethylene and .Iadd.4 to 20 percent by weight of .Iaddend.a higher .Iadd.C 3-8  .Iaddend.alpha-olefin .[.containing 4 to 20 percent by weight of the higher alpha-olefin.]., .Iadd.in the presence of a catalyst containing a compound of a transition metal of sub-groups IVa, Va and VIa of the Periodic Table of Elements, the said catalyst being activated by an organometallic compound, this process .Iaddend.comprising treating the co-polymer thermomechanically in the molten state at a temperature less than 220° C., in the presence of an organic peroxide which produces free radicals, in which the organic peroxide is employed in an amount within the range of 0.005% to 1% by weight of the co-polymer, such that the treated co-polymer has a branching index within the range of 0.8 to 0.95 and its gelling rate, as measured by extraction with boiling xylene, is zero. 
     
     
       2. A process as claimed in claim 1 in which the organic peroxide is employed in an amount within the range of 0.02% to 0.2% by weight of the co-polymer. .[.3. A process as claimed in claim 1 in which the co-polymer is obtained from a mixture of ethylene and a C 3  -C 8  alpha-olefin by copolymerization in the presence of a catalyst containing a compound of a transition metal of sub-groups IVa, Va, VIa of the Periodic Table of 
     
     
        Elements..]. 4. A process as claimed in claim .[.3.]. .Iadd.1 .Iaddend.in which the alpha-olefin is selected from the group consisting of propylene, 
     
     
        n-butene-1, methyl-4-pentene-1, n-hexene-1, and n-octene-1. 5. A process as claimed in claim 1 in which the organic peroxide is selected from the group consisting of di-terbutyl peroxide, dicumyl peroxide, .[.2,5-dimethyl-.].2,5-dimethyl-2,5-di(terbutylperoxy)-hexane, 2,5-dimethyl-2,5-di(terbutylperoxy)-hexyne, butyl-4,4-bis(terbutylperoxyvalerate), dicumyl hydroperoxide, 1,1-bis(terbutylperoxy)-3,3,5-trimethylcyclohexane, 
     
     
        1,3-di(terbutylperoxy)di-isopropylbenzene. 6. A process as claimed in claim 1 in which the co-polymer is subjected to the thermomechanical treatment in two stages at temperatures within the range of 130° C. to 220° C., the first stage of the treatment being carried out at a temperature at which the organic peroxide used has a half-life period greater than 13 times the duration of this first treatment stage, the second stage of treatment being carried out at a temperature at which the organic peroxide used has a half-life period of less than 0.4 times the 
     
     
        duration of this second treatment period. 7. Co-polymers prepared by the 
     
     
        process of claim 1. 8. Film formed of the co-polymers produced by the method of claim 1.