Low Density Polyethylene Polymeric Compositions

The present invention relates to crosslinked polymers, especially blends of polymers, and shaped articles constructed therefrom. In particular, the present invention relates to crosslinked polyethylenes.

It is known that the properties of polymers may be considerably modified by crosslinking of the polymer chains. This is particularly true of polyethylenes which, in crosslinked form, have found important commercial applications.

The present invention is based on the finding that a certain class of polyethylenes, when crosslinked, exhibits substantial advatages.

Accordingly, the present invention provides a substantially cross-linked polymeric composition comprising a linear low density ethylene homo- or copolymer which, prior to cross-linking, is characterised by a density at 25.degree. C. of 0.940 gm/cm.sup.3 or less and a linearity expressed in terms of pendant methyl groups per 10.sup.3 carbon atoms of the polymer chain of less than 30 with a substantial absence of long chain branches. For the avoidance of doubt, the term "copolymer" as employed herein is used in a broad sense to mean polymers produced from at least two different monomeric species and to include terpolymers and the like.

The ethylene homo- or copolymer preferably has a density at 25.degree. C. prior to crosslinking of from 0.916 to 0.940 gm/cm.sup.3, particularly from 0.919 to 0.940 gm/cm.sup.3 especially less than 0.930 gm/cm.sup.3 e.g. from 0.919 to 0.930 gm/cm.sup.3.

The degree of branching of the polymeric chains prior to cross-linking is expressed in terms of the average number of pendant methyl groups per 10.sup.3 carbon atoms of the ethylene homo- or copolymer chain which, as will be appreciated, is a measure of all side groups which contain a methyl group, e.g. any alkyl group and may be determined in accordance with known analytical procedures, for example the infra-red analytical technique reported by A. H. Willbourn in J. Poly. Sci 1959 34 569. Preferred polymers are those having 10 or less pendant methyl groups per 10.sup.3 carbon atoms of the polymer chain and those having 15 to 30 pendant methyl groups per 10.sup.3 carbon atoms of the polymer chain. Preferably the polymer contains on average less than 20 pendant methyl groups per 10.sup.3 carbon atoms of the polymer chain.

The ethylene homo- or copolymers are characterised by a substantial absence of long chain branches and preferably have no more than 5 long chain branches and more preferably no more than 1 long chain branch, on average per 10.sup.3 carbon atoms of the polymer chain. By long chain branches as employed herein is preferably meant branches greater in length than C.sub.8 more preferably greater in length than C.sub.6.

The degree of long chain branching may, for example, be established by computing the differences between the number of short branches, determined for example, by .sup.13 C nuclear magnetic resonance spectroscopy, in accordance with the method reported by M. E. A. Cuddy and A. Bunn in Polymer, 1976 Vol, 17 April page 345, and the total number of branches determined as pendant methyl groups by infra-red spectroscopy.

Of particular interest are those polymers wherein substantially all branches are C.sub.2 to C.sub.6 branches especially C.sub.2 branches.

The linear low density ethylene homo or copolymers of the invention may be distinguished from the conventional, i.e. branched, low density polyethylenes by their higher .DELTA.T values where .DELTA.T as employed herein is defined as the difference in .degree.C. between the temperature at which the polymer melts and the temperature at which the onset of crystallisation occurs. Typically .DELTA.T values of greater than 15.degree. C., for example 15.degree. to 20.degree. C. particularly 16.degree. to 20.degree. C., are observed in the linear low density ethylene homo or copolymers employed in the compositions of the invention.

The linear low density ethylene homo or copolymers of the invention may be characterised by their molecular weight distribution index (Mw/Mn) as measured by standard methods (e.g. GPC). Thus the polymers of special interest are characterised by a molecular weight distribution index of below 8 and preferably in the range 3 to 8 e.g; 3 to 7. A related parameter is the stress exponent, the polymers of interest being characterised by a stress exponent in the range 1.20 to 1.40 where stress exponent is defined as ##EQU1##

A further characteristic feature of the polymers employed in the compositions in accordance with the invention is their degree of unsaturation particularly in terms of terminal vinyl groups per 10.sup.3 carbon atoms of the polymeric chain, values of at least 0.2, particularly 0.2 to 1.5 for example 0.3 to 1.5 as measured for example by infra-red spectroscopy being typical.

The degree of cross-linking of the compositions may be expressed in terms of the gel content (ANSI/ASTM D2765-68). Preferably the gel content of the cross-linked compositions is at least 40%, more preferably above 50%, particularly above 65% and up to 95%, of the polymeric components of the composition.

The cross-linked compositions of the invention may be further characterised by their high elongation versus modulus performance. Thus typical elongation at break values at 150.degree. C. exceed 300%, for example 300 to 1000%, for filled and unfilled cross-linked compositions having a 100% secant modulus at 150.degree. C. in the range 3.5 to 4 Kg/cm.sup.2 measured in accordance with ASTM D 1708-66. Preferred compositions are characterised by elongation at break values at 150.degree. C. of at least 300%, particularly at least 500%, for example at least 600%, 700%, 800%, and often 900% for cross-linked compositions having at 100% secant modulus at 150.degree. C. in the range 3.5 to 4 Kg/cm.sup.2.

Ethylene copolymers which may be employed in the compositions of the invention are preferably low density copolymers of ethylene with olefinically unsaturated monomers polymerizable therewith. Suitable such monomers are C.sub.3 to C.sub.20, preferably C.sub.3 to C.sub.8, olefins, preferably .alpha.-olefins such as n-propyl-1-ene, n-but-1-ene, n-pent-1-ene, n-hex-1-ene, n-hept-1-ene and n-oct-1-ene, or olefinically unsaturated esters such as C.sub.2 -C.sub.8 alkenyl C.sub.2 -C.sub.8 carboxylic acid esters for example vinyl acetate and C.sub.1 -C.sub.8 alkyl C.sub.3 -C.sub.8 alkenoates for example ethyl acrylate. Copolymers preferably contain greater than 50 weight percent, more preferably greater than 60 weight percent, for example greater than 70 weight percent, especially greater than 85 weight percent, for example 95 to 98 weight percent, ethylene, the optimum amount depending of course on the comonomer employed.

Random, block or graft copolymers may be employed, particularly random copolymers.

Of special interest in the compositions of the invention are blends of the linear ethylene homo or copolymers with other homo- or copolymers blended prior to cross-linking. Examples of suitable homo- or copolymers which may be blended into the compositions include thermoplastic polymers, particularly other polyethylenes, for example branched low density polyethylenes especially those having at least 5 more preferably at least 10 long chain branches (e.g. greater than C.sub.10 preferably greater than C.sub.20) per 10.sup.3 carbon atoms of the polyethylene chain such as those having on average at least 5 more preferably at least 10 especially at least 15 pendent methyl groups per 10.sup.3 carbon atoms of the polyethylene chain (particularly those polyethylenes having at least 20 more preferably at least 40 branches greater in length than C.sub.200 per average molecule), and a density at 25.degree. C. below 0.940 gm/cm.sup.3 for example in the range 0.910 to 0.940 gm/cm.sup.3, or linear high density polyethylenes having on average less than 20 preferably less than 15, for example less than 10, especially 0.5 to 5, pendent methyl groups per 10.sup.3 carbon atoms of the polyethylene chain and a density at 25.degree. C. greater than 0.940 gm/cm.sup.3 for example 0.941 to 0.960 gm/cm.sup.3, other polyolefins for example polypropylene, and copolymers for example ethylene/propylene copolymers and EPDM terpolymer.

Further examples of suitable blend polymers include elastomeric polymers particularly silicone elastomers as well as copolymers of ethylene with ethylenically unsaturated aliphatic esters, especially such copolymers when substantially free of halogen-containing substituents. Preferred elastomeric polymers are those exhibiting a characteristic rubber-like elastic deformability under the action of comparatively small stress the material returning substantially to its undeformed state on the removal of the applied stress, particularly those which in the uncross-linked state have an elastic modulus of 30N/mm.sup.2 or less, measured at room temperature in accordance with the method described in ASTM D638-72.

The preferred elastomers for use in the present invention are ethylene/acrylic ester copolymers and ethylene/vinyl acetate copolymers, especially those containing at least 3.6 moles of ethylene per 1000 grams of polymer. Examples of suitable elastomers include:

(a) An ethylene/alkyl acrylate or ethylene/alkyl methacrylate copolymer, wherein the alkyl group has 1-4 carbon atoms; the proportion of the acrylic ester being about 2.5-8.0 moles of ester groups per kilogram of the copolymer.

(b) A terpolymer of ethylene with an alkyl acrylate or methacrylate wherein the alkyl group has 1-4 carbon atoms and a third copolymerizable monomer, which may be, for example one of the following:

(i) a C.sub.1 -C.sub.12 alkyl monoester or diester of a butenedioic acid,

(ii) acrylic acid,

(iii) methacrylic acid,

(iv) carbon monoxide,

(v) acrylonitrile,

(vi) a vinyl ester,

(vii) an alkyl acrylate or alkyl methacrylate, the alkyl group having at least five carbon atoms; and

(viii) maleic anhydride; or

(c) Ethylene/vinyl acetate copolymers especially those containing at least 35% by weight vinyl acetate.

In the above terpolymer the proportion of the acrylic ester is equivalent to about 2.5-8.0 moles of ester groups per kilogram of the polymer, and the proportion of the third monomer is no higher than about 10 weight percent of the polymer.

The elastomer can be a simple copolymer of ethylene with methyl acrylate, ethyl acrylate, propyl acrylate isopropyl acrylate, a butyl acrylate, methyl methacrylate, ethyl methacrylate, propyl methacrylate, isopropyl methacrylate, a butyl methacrylate or vinyl acetate. Such copolymers that are not commercially available can be made by conventional and well known methods. These copolymers preferably have a melt index within the range of 0.1-70 at 190.degree. C., more preferably 0.5-15 as measured by ASTM method number D-1238-52T, or the substantially equivalent method ASTM D-1238-73.

The terpolymer of ethylene with an acrylic ester and a third monomer may contain as the third monomer an ester or half ester of fumaric acid or maleic acid, wherein the alcohol moiety can be, for example, methyl, ethyl, propyl, isopropyl, various isomers of butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl and the like. The third monomer may also be, among others, a vinyl ester such as, for example, vinyl acetate or vinyl butyrate. It can also be an acrylic ester such as, for example, various isomeric forms of pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, pentadecyl and octadecyl acrylate and methacrylates. It is not practical to use as the third monomer an acrylic ester in which the alcohol moiety contains more than 18 carbon atoms.

Excellent results have been obtained using as the elastomer component of the polymer composition of a terpolymer of ethylene, methyl acrylate and a cure-site monomer comprising carboxyl groups available from Du Pont under the trade name Vamac.

Physical properties and other details concerning this material are to be found in a brochure available from Du Pont entitled "Vamac ethylene/acrylic Elastomers--A new Class of Heat & Oil Resistant Rubber" by J. F. Haymon, R. E. Fuller, W. K. Witsiepe and R. N. Greene under reference BA-0002, the disclosure of which is incorporated herein by reference, corresponding essentially to articles appearing in Rubber Age, May 1976, and De Nederlands Rubberindustrie No. 7177.

Mixtures of any of the above mentioned elastomers with each other or with other elastomers may be used where appropriate although it has been found that the presence of hydrocarbon elastomers has a deleterious effect upon the oil resistance of the polymer composition and thus these are preferably not included, or if present, are preferably incorporated in an amount of not more than 5% by weight based on the total weight of the polymer composition.

It is believed to be advantageous for the solubility parameter of the elastomer to be greater than 9, and, in advantageous compositions according to the invention, it is further preferred that the solubility parameters of the polymeric components of the blend should be similar, e.g. they will differ by not more than 0.5, preferably by not more than 0.25.

For the purpose of this specification, solubility parameter is defined as that measured by the method of Brandrup & Immergut, Polymer Handbook Chapter 4 page 340 (2nd Edition) and is expressed as (cals/cm.sup.3).sup.1/2.

Some types of polymer materials inherently have a solubility parameter greater than 9 whereas others can have solubility parameters greater than or less than 9 depending on their precise chemical composition. Still others, of course, have solubility parameters which are inherently less than 9.

The cross-linked polymeric compositions of the invention which have been derived from blends of linear low density homo or copolymers with thermoplastic or elastomeric homo- or copolymers offer various unforeseen advantages and are accordingly of special interest. Thus reduced hot creep and hot tension set phenomena are typically exhibited by the blend compositions, particularly the blends with other polyethylenes, considerably facilitating moulding of the compositions. In addition cross-linking may be more readily achieved, particularly the blends with other polyethylenes such as branched low density polyethylenes, for example after incorporating from 5 to 50 weight percent of the blend polymer. The blend polymers frequently offer increased thermal ageing and resistance to hydrocarbon fluid particularly where the solubility parameter of the blend component exceeds 9, for example blends with elastomers such as ethylene/vinyl acetate.

Preferably the weight ratio of the blended polymeric component or components to the linear low density ethylene homo- or copolymer in the composition lies in the range 0 to 20:1 particularly 0 to 1:1, more preferably 0 to 0.5:1, especially 0 to 0.2:1, for example 0 to 0.15:1 respectively.

The preferred blends have a density at 25.degree. C. below 0.960 gm/cm.sup.3, especially below 0.940 gm/cm.sup.3 with branched low density polyethylenes. In some cases blends with a density at 25.degree. C. of below 0.925 gm/cm.sup.3 exhibit particularly interesting properties especially high elongation at break versus 100% secant modulus at 150.degree. C. properties.

Particularly interesting linear low density ethylene homo or copolymers, including blends, are the resins commercially available from E. I. Du Pont de Nemours (Canada), Corruna, Ontario under the trade name "Sclair" and in particular the resins listed below in Table 1 under type reference.

Examples of linear low density polyethylene homo- or copolymers including blends of special interest are further characterised in Table 2.

Examples of other linear low density polyethylenes are those commercially available from Gulf Oil under the Gulf type references set out in Table 3.

For most purposes, it is preferred that the compositions incorporate at least 10 weight percent filler, either reinforcing fillers (e.g. of particle size from 0.01 to 1 micron) or non-reinforcing fillers (e.g. of particle size from 1 to 120 microns). It is generally found that a higher degree of reinforcement is secured by the use of reinforcing fillers such as high surface area carbon blacks or silicas than would be obtained with other types of polyethylenes and that usually no significant detriment to physical properties are observed with non-reinforcing fillers such as calcium carbonate or thermal black, as would be observed in other types of polyethylenes.

The compositions of the invention may include other additives, such as stabilizers, for example UV stabilisers and antioxidants, flame retardants, anti-tracking fillers and pigments, the nature and amounts of additives included depending naturally on the specific use for which the compositions are intended.

The compositions of the invention may be produced in conventional manner e.g. by milling the components in a Banbury mixer. They may then be processed into shaped articles e.g. by extrusion or moulding. Shaped articles so produced also form part of the present invention. When it is proposed to cross-link the compositions of the invention in the solid state, e.g. by exposure to ionising radiation, preferably the compositions are quenched after the hot shaping stage, at least across the crystalline melting point of the composition. Preferably quenching rates of at least 5.degree. C./sec, e.g. at least 10.degree. C./sec, more preferably at least 20.degree. C./sec and in the case of thin articles such as films advantageously at least 100.degree. C./sec, are employed. Quenching may be achieved by contacting the shaped article with a heat exchange fluid such as water. It has been found that quenching achieves a decrease in crystallinity and thereby an increase in modulus e.g. 2% secant modules, in the cross-linked material.

Cross-linking preferably takes place at or subsequent to the shaping stage, depending on the manner of cross-linking and the nature of the shaped article. It may be effected by the incorporation of from 0.2 to 5 weight percent of a cross-linking agent such as a free radical initiator for example an organic peroxide, such as dicumyl peroxide or 2,5-di-(t-butyl-peroxy)hexane, alone or in combination with a cocuring agent such as a poly-functional vinyl or allyl compound, for example triallyl cyanurate, triallyl isocyanurate or pentaerythritol tetra-methacrylate. One preferred mode of chemically cross-linking involved grafting a hydrolysable silane or silane derivatives e.g. an alkoxysilane such as vinyl trimethoxysilane to the polyethylene base structure and subsequently hydrolysing to effect cross-linking by silanol condensation in manner known per se. Catalysts may be employed to facilitate silanol condensation e.g. organotin catalysts such as dibutyltindilaurate.

Alternatively, cross-linking may be effected by exposure to high energy irradiation such as an electron beam or .gamma.-rays. Dosages in the range 2 to 80 Mrads, preferably 5 to 50 Mrads, e.g. 8 to 20 Mrads are appropriate. For the purposes of cross-linking by irradiation, preferably from 0.2 to 5 weight percent or a pro-rad such as a poly-functional vinyl or allyl compound, for example triallyl cyanurate or triallyl isocyanurate are incorporated into the composition prior to the cross-linking treatment.

The above mentioned non-cross-linked compositions incorporating an effective amount of a cross-linking agent or prorad are new and also form part of the present invention.

The compositions of the present invention are particularly suitable for the production of dimensionally recoverable articles, that is to say, articles, the dimensional configuration of which may be made substantially to change when subjected to an appropriate treatment. Of particular interest are heat recoverable articles, the dimensional configuration of which may be made substantially to change when subjected to heat treatment. Heat recoverable articles may be produced by deforming a dimensionally heat stable configuration to a heat unstable configuration, in which case the article tends to assume the original heat stable configuration on the application of heat alone. As is made clear in U.S. Pat. No. 2,027,962, however, the original dimensionally heat stable configuration may be a transient form in a continuous process in which, for example, an extruded tube is expanded, whilst hot, to a dimensionally heat-unstable form. Alternatively a preformed dimensionally heat stable article may be deformed to a dimensionally heat-unstable form in a separate stage. In the production of dimensionally recoverable articles, the composition may be cross-linked at any stage in the production process that will accomplish the desired dimensional recoverability e.g. prior to the shaping of the dimensionally unstable configuration. One manner of producing a heat recoverable article comprises shaping the pre-cross-linked composition into the desired heat stable form subsequently cross-linking the composition, heating the article to a temperature above the crystalline melting point of the composition, deforming the article and cooling the article whilst in the deformed state so that the deformed shape of the article is retained. In use, since the deformed state of the article is heat unstable, application of heat will cause the article to assume its original heat stable shape. Such dimensionally recoverable articles may be employed as sleeves for covering and sealing splices and terminations in electrical conductors, for environmentally sealing damaged regions or joints in utility supply systems, e.g. gas or water pipes, district heating systems, ventilation and heating ducts and conduits or pipes carrying domestic or industrial effluent.

The compositions of the present invention are also particularly suitable for the production of insulation material, particularly jacketing materials for wires and cables. Such materials may be produced in conventional manner, for example by extrusion onto conductors to form wires or onto wires to form cables with simultaneous or subsequent cross-linking.

They are also useful as high voltage insulation incorporating an anti-tracking filler such as alumina trihydrate especially to achieve an initial tracking voltage according to ASTM D2303 of greater than 2.5 kV and/or when including as a blend component, in the linear low density ethylene homo- or copolymer, silicone elastomers or ethylene copolymers. Suitable antitracking fillers and blendable silicone elastomers and ethylene copolymers are described by R. J. Penneck and R. J. T. Clabburn in "Heat Shrinkable Cable Termination System for High Voltage Cables" Proc. 10th Electrical Insulation Conference, Chicago USA Sept. 20-23 1971, page 292-297 and in UK Pat. Nos. 1,303,432 and 1,137,952 the contents of which are incorporated herein by reference.

Furthermore, by the incorporation of appropriate fillers, e.g. carbon black, the compositions may be rendered semiconducting or conducting and in such form are particularly suitable as semi-conductive or conductive polymers for use in electrical heating materials, e.g. in the form of heating tapes, strips or panels, in the electrical screening of electrical power cables or in the electrical stress relief of splices and termination in high voltage electric cables.

Another important application of the cross-linked compositions of the invention is in the production of semi-permeable membranes. For such use the compositions of the invention are produced in film form preferably with a film thickness of less than 1.0 mm, more preferably in the range 0.001 to 0.5 mm. The film is also preferably grafted with monomers designed to modify the selectivity of the membrane to vary the permeability thereof to various ionic species. Examples of graftable monomers include olefinically unsaturated acids or derivatives thereof, particularly methacrylic and acrylic acids. Such grafting may be accomplished in known manner by subjecting the film to high energy radiation, e.g. to an electron beam, U.V. or .gamma.-radiation in the presence of the monomeric species to be grafted. The film may be in non-cross-linked form prior to exposure to the radiation such that the radiation treatment serves also to cross-link the composition. Preferably, however, the film is cross-linked prior to grafting to achieve better ion-selectivity.

Membranes produced in accordance with the invention are particularly useful as separators in electrochemical processes, for example as separators in electrolytic cells and particularly batteries such as Ag/Zn, Hg/Zn, Ni/Cd and Ni/Zn cells. Such membranes possess several advantages such as longer service life in electrolytic cell environments, improved wet strength and lower swelling tendency than conventional polyethylene membranes.

The compositions are particularly useful in any of the above applications in view of their notable ability to accept loadings of additives, particularly fillers, e.g. 10 weight percent or more, without detriment to the properties of the composition, their notable mechanical properties in cross-linked form, e.g. elongation at break, hot modulus, abrasion resistance and tensile strength, and/or their chemical resistance, e.g. to solvents, particularly organic solvents such as oil and petroleum jelly.

The invention is illustrated by the following examples wherein parts and percentages are by weight and temperatures are in .degree.C.

Various cross-linked compositions are produced by milling the ingredients of each formulation (see below) together on a twin roll mill to form a hide. The hides are pressed into uniform plaques and cured at 200.degree. C. for 10 minutes. The ingredients of the various formulations employed are set out below:

The tensile properties of the resultant plaques are set out below and determined by standard test methods:

The following formulations A and B were melt extruded at 195.degree. at which temperature grafting of the silane onto the polyethylene base structure is initiated via the decomposition of the peroxide.

80 parts: Sclair 8105

20 parts: DYNH-3 (trade name--a branched low density polyethylene available from Union Carbide)

2 parts: Vinyltrimethoxysilane

0.1 parts: Dicumyl peroxide

100 parts: DYNH-3

2 parts: Vinyltrimethoxysilane

0.2 parts: Dicumyl peroxide

The resulting material was cooled and pelletised.

The following formulation C was also melt extruded and pelletised:

100 parts: DYNH-3

1 part: Dibutyltindilaurate

2 parts: Santanox R (trade name--an antioxidant available from Monsanto Ltd)

95 parts of pelletised formulation A were blended with 5 parts of pelletised formulation C and injection moulded into short tube sections. The resulting tube sections were allowed to cool, and then immersed in water at 80.degree. for 24 hours. The procedure was repeated for a blend of formulations B and C.

The materials produced from formulation A were found to possess substantially superior elongation at 150.degree. than those produced from formulation B.

Plaques are made up in analogous manner to that described in Example 1 from commercial grade Sclair linear low density polyethylenes (11W, 11D, 8105, 8305 and 8405) and Gulf 9633 and 9636 linear low density polyethylenes in the absence of any additive other than any already present in the commercial grade product. Instead of the heat cure step of Example 1, the plaques are exposed to electron beaming at radiation dosages of 10, 15, 20 and 25 Mrads. Thereafter, the various plaques are examined to determine their 100% secant modulus at 150.degree.. For comparison purposes, the procedure was repeated with the following commercially available branched low density polyethylenes i.e. DYNH-3, PN220 (BXL) and CARLONE 30-002BA (Shell). The results are set out graphically in FIGS. 1 and 2 and define two envelopes, one characteristic of the linear low density polyethylenes and the other characteristic of the branched low density polyetheylenes. These figures demonstrate the greater ability of the linear low density polyethylenes to crosslink at any given radiation dosage than the branched low density polyethylenes (FIG. 1) and the superior hot properties of the crosslinked linear low density polyethylenes than the crossliked conventional branched low density polyethylenes (FIG. 2).

The procedure of Example 3 is repeated incorporating 0.2% of triallyl cyanurate as prorad in each product prior to cross-linking. Results are slightly improved over those obtained in Example 3.

In order to demonstrate how ethylene homo and copolymers employed in the compositions of the invention are distinguished from branched low density polyethylenes, accompanying FIG. 3 shows a plot of AT (T.sub.m -T.sub.c) versus density at 25.degree. C. values for the linear low density Dupont Sclair resins 11W.sup.1, 8105.sup.2, 8107.sup.3, 8305.sup.5 and 8405.sup.6 against commercially available branched low density polymers DYNH-3.sup.7 (Union Carbide), PN 220.sup.8 (BXL) Carlona 25-002GA.sup.9 (Shell), Carlona 30-002BA.sup.10 (Shell), EXXON LT-117.sup.11 (EXXON) and Gulf 2604M.sup.12 (Gulf Oil), the materials being represented on the Figure by the superscripts 1 to 12.

Example 3 is repeated at radiation dosages of 10, 15 and 20 Mrads or plaques made up from blends of commercial grade Sclair linear low density polyethylenes with varying amounts of a conventional branched low density polyethylene and the 100% secant modulus at 150.degree. C. determined for each plaque. The results are shown graphically in FIG. 4 indicating a synergistic effect in 100% secant modulus properties at 150.degree. for cross-linked mixtures of linear and branched low density polyethylenes.

A formulation of the following composition:

Sclair 8405: 62.55 parts

Whiting G400: 30.00 parts

Vulcan 9: 3.00 parts

Zinc stearate: 1.50 parts

Maglite D: 1.50 parts

Irganox 1010: 1.25 parts and

Triallyl cyanurate: 0.20 parts

is formed into tubing in a laboratory extruder under the following operating conditions:

barrel temperature zone 1: 120.degree.-130.degree.

barrel temperature zone 2: 130.degree.-140.degree.

die temperature: 140.degree.-150.degree.

die diameter: 25.+-.1 mm

wall thickness: 1.+-.0.01 mm

haul off speed: 0.4 meters/minute

The extruded tubing is subjected to a dosage of 10 Mrads electron beaming in an electron accelerator and then cut into 20 cm lengths. Each length is expanded after heating, on a former to give 500% expansion as measured by change in wall thickness. The resulting heat shrinkable product is suitable for shrinking onto a substrate of from 26 to 120 mm diameter without danger of splitting. The example is repeated with the additional stage of quenching the extruded tube by immersion in water as soon as it leaves the extruder thereby achieving an increase in modulus of the material after cross-linking.

The procedure of Example 7 is repeated employing the following formulation.

The sleeve so produced could be expanded to greater than 600% without exhibiting split sensitivity and in addition an excellent balance of properties is achieved. Typical properties are set out below.

150.degree. C. Properties

100% secant modulus: 0.35-0.40 MPa

Tensile strength: 0.95 MPa

Elongation: >430%

Room Temperature Properties

Tensile strength: 24.5 MPa

Elongation: 590%

2% Secant modulus: 130.0 MPa

-40.degree. C. Properties

Tensile strength: 29.0 MPa

Elongation: 365%

Heat Ageing (168 hours at 150.degree. C.)

Tensile strength: 22.4 MPa

Elongation: 525%

Solvent Resistance (168 hours Petroleum Jelly 70.degree. C.)

Tensile strength: 18.5 MPa

Elongation: 532%

Electrical Properties

Electrical strength: 161 Kv/cm

Permativity: 3.14

Volume Resistivity: 7.7.times.10.sup.13 ohm cm

Water Uptake: 0.21%

Specific Gravity: 1.057 g/cm.sup.3

The procedure of Example 7 is repeated employing a formulation of the following composition

Sclair 8105: 61.55 parts

Thermax (trade name--a thermal carbon black available from Vanderbilt Ltd): 30.00 parts

Zinc stearate: 1.50 parts

Maglite D: 1.50 parts

Irganox 1010: 1.25 parts

Triallyl cyanurate: 0.20 parts

The resulting semi-conductive heat shrinkable tube may be employed in the stress grading of the termination in a screened high voltage cable.

The procedure of Example 7 is repeated employing the following formulation

The conductive sleeve so produced possesses an excellent balance of properties, allowing its use as a screen for electrical cables, typical properties being set out below

Room Temperature

Tensile strength (MPa): 19.57

Elongation (%): 325

150.degree. C.

Tensile strength (MPa): 2.3

Elongation (%): 365

100% secant modulus (MPa): 0.8

Heat Shock: 4 hrs @ 200.degree. C.

Elongation (%): 275

Heat ageing: 7 days @ 150.degree. C.

Elongation (%): 225

Solvent Resistance: days

Transformer Oil:

Elongation (%): 270

Specific Gravity: 1.086

Volume Resistivity (ohm cm): 6.0

The procedure of Example 7 is repeated employing the following high voltage anti-tracking insulation formulations:

The sleeves so produced were found to have the following properties.

As will be observed, the sleeve produced from the linear low density polyethylene (Formulation 2) is significantly superior in all its physical properties particularly elongation at break at 150.degree., to that produced from the branched low density polyethylene (Formulation 1) whilst retaining the high anti-tracking property according to ASTM D 2303.

Sclair 8405: 74.5 parts

Timinox (antimony trioxide): 8.0 parts

Chlorowax (Hoeschst): 16.0 parts

Agerite Resin D (Vanderbilt): 1.5 parts

was extruded onto a heated copper conductor (110.degree. C.) to yield a jacket having excellent insulation characteristics and particularly good mechanical properties e.g. high abrasion resistance.

Sclair 11D was extruded as a film 0.025 mm thick under the following extrusion conditions:

Zone 1: 140.degree.

Zone 2: 165.degree.

Zone 3: 175.degree.

Die: 175.degree.

Blow up ratio: 2.5:1

The resulting film is immersed in a solution comprising by volume 55% benzene, 5% carbon tetrachloride and 40% acrylic acid and irradiated with .gamma.-radiation to a dosage of 0.5 Mrads at a dosage rate of 0.05 Mrads per hour. The film is washed with a 40% aqueous solution of potassium hydroxide. The resulting film is emminently suitable for use as a battery separator having an areal resistivity in 40% aqueous potassium hydroxide of 0.1 to 0.2 ohm/cm.sup.2 and excellent mechanical properties, for example tensile strength.

The following compositions were blended employing a laboratory Banbury internal mixer.

Vamac N123 (Trade name--an ethylene/methyl acrylate elastomer available from Dupont and having a solubility parameter of 9.1): 30

Carbon black: 2

Antimony trioxide: 6

Decabromodiphenylether: 12

Crodamine IHT (Trade name--a release agent available from (Crode Ltd): 0.375

Irganox 1010: 0.375

Triallyl cyanurate: 1

Whiting G400: 16

Sclair resin: 30

The Sclair resin, Vamac N123 and Irganox 1010 were loaded into the mixer and mixed at room temperature for 1 minute. The carbon black, antimony trioxide, decabromodiphenylether and calcium carbonate were then added and mixed until temperature of the mix rose to 140.degree.. Crodamine IHT and triallyl cyanurate were then introduced and mixed in for 45 seconds. This mix was then put onto a mill and sheeted off. Compression moulded plaques were made from the sheeted material and irradiated with an electron beam to a dosage of 12 Mrads. The plaques were tested for heat shock resistance (4 hours at 200.degree. C.) and for resistance to ASTM Oil No. 2 and diesel oil by immersion in the fluids for 24 hours at 90.degree.. The results are set out below. As a comparison the sclair resin is replaced by DYNH-3.