Halogen-free decorative homogeneous surface coverings

Abstract

Halogen-free decorative surface covering compositions comprising a polymer blend, the polymer blend comprising: a) at least one thermoplastic elastomer, the thermoplastic elastomer being a block copolymer comprising hard and soft sequences, wherein the hard sequence is a (co)polymer of one or more vinyl aromatic monomer(s) and wherein the soft sequence is a (co)polymer of one or more alkylene(s) or of a mixture of one or more alkylene(s) and one or more vinylaromatic monomers; b) at least one thermoplastic polyurethane.

Claims

1. Process for the preparation of a halogen-free decorative surface covering, comprising the steps of: i. providing a plurality of single coloured strands, each single coloured strand comprising a polymer blend, which comprises: a) at least one thermoplastic elastomer, said thermoplastic elastomer being a block copolymer comprising hard and soft sequences, wherein the hard sequence is a (co)polymer of one or more vinyl aromatic monomer(s) and wherein the soft sequence is a (co)polymer of one or more alkylene(s) or of a mixture of one or more alkylene(s) and one or more vinylaromatic monomers; b) at least one thermoplastic polyurethane; ii. granulating each single coloured strand separately to form single coloured granules or merging the plurality of single coloured strands and granulating the merging outcome to form multi coloured marbled granules; iii. converting said single or multi coloured marbled granules into a multi coloured halogen-free surface covering.

2. The process according to claim 1 wherein the each single coloured strand is provided by mixing and compounding components of the polymer blend, wherein the compounding is performed at a temperature comprised between 140 and 220° C.

3. The process according to claim 1 wherein the merging outcome of step ii) is obtained from calendering or extruding the plurality of single coloured strands.

4. The process according to claim 1 wherein the calendering in step ii) is performed at a temperature comprised between 110 and 160° C.

5. The process according to claim 1 wherein the extruding in step ii) is performed at a temperature comprised between 40 and 150° C.

6. The process according to claim 1 wherein step iii) comprises pressing using a belt press and wherein the belt press operates at: a temperature comprised between 130 and 220° C.; a speed comprised between 2 and 25 m/min, preferably between 10 and 18 m/min; a pressure comprised between 3 and 20 bar.

7. The process according to claim 1 wherein step iii) comprises calendering using a calender, and wherein the calender operates at: a temperature comprised between 130 and 220° C.; a speed comprised between 2 and 25 m/min.

8. The method according to claim 1 comprising the additional step of contacting the multi coloured halogen-free surface covering with a topcoat layer said topcoat layer comprising a cross-linked material.

9. The method according to claim 1, wherein the topcoat layer is obtained from curing a radiation curable coating composition, said radiation curable composition comprising ethylenically unsaturated acrylic, ester, ether or urethane comprising polymers, oligomers or monomers.

10. The method according to claim 1, wherein the at least one thermoplastic elastomer (a) comprises between 10 and 70% by weight.

11. The method according to claim 1, wherein the at least one thermoplastic elastomer (a) comprises from 30 to 90% by weight of at least one vinyl aromatic monomer.

12. The method according to claim 1, wherein the at least one thermoplastic elastomer (a) is selected from the group consisting of styrene-butadiene-styrene, styrene-isoprene-styrene, styrene-isobutylene-styrene, styrene-ethylene-butylene-styrene and styrene-ethylene-propylene-styrene.

13. The method according to claim 1, wherein the at least one thermoplastic polyurethane (b) comprises an aromatic thermoplastic polyurethane.

14. The method according to claim 1, wherein each single coloured strand comprises from 25 and 70% by weight of the polymer blend, said polymer blend comprising from 60 to 20% by weight of thermoplastic elastomer (a) and from 40 to 80% by weight, preferably from 50 to 70% by weight of thermoplastic polyurethane (b), the sum of (a) and (b) being 100%.

15. The method according to claim 1, wherein each single coloured strand comprises from 20 to 70% by weight of one or more filler(s) and from 0.1 to 10% by weight of the one or more pigments and/or dyes.

16. The method according to claim 1, wherein each single coloured strand comprises from 0.5 to 5% by weight of one or more silicones selected from the group consisting of the siloxane homopolymers or copolymers comprising dimethylsiloxane units, methylhydrogen siloxane units, diphenylsiloxane units, phenylmethylsiloxane units, dimethylhydrogen siloxane units and trimethylsiloxane units.

17. The method according to claim 1, wherein said thermoplastic elastomer (a) and said thermoplastic polyurethane (b) together constitute 100% of said polymer blend.

18. The method according to claim 14, wherein each single coloured strand comprises between 30 and 75% by weight of one or more ingredients selected from the group consisting of lubricants, compatibilizers, silicones, antioxidants, fillers, pigments, dyes and additives, wherein the polymer blend and the one or more ingredients together constitute 100% of each single coloured strand.

Description

DETAILED DESCRIPTION OF THE INVENTION

(1) Decorative surface coverings include any design covering such as floor-, wall- and ceiling coverings.

(2) The decorative surface coverings of the present invention are substantially halogen free what the expression “halogen free” has to be understood as devoid of any halogen comprising polymers, without excluding the presence of halogen comprising impurities or halogen comprising additives present in a concentration of less than 1 percentage.

(3) The decorative surface coverings of the present invention comprise a blend of one or more thermoplastic elastomer and one or more thermoplastic polyurethanes.

(4) The one or more thermoplastic elastomers are block copolymers comprising hard and soft blocks, wherein the hard blocks are obtained from the polymerisation of one or more vinyl aromatic monomer(s) and wherein the soft blocks are obtained from polymerisation of one or more alkylene(s) or the copolymerisation of one or more alkylene(s) and one or more vinyl aromatic monomer(s).

(5) The vinyl aromatic monomer is selected from the group consisting of styrene and α-methyl styrene wherein the benzene ring may be substituted by one to three (C1-C4) alkyls, preferably methyl or ethyl groups or vinylnaphthalene optionally substituted by one or more methyl or ethyl groups.

(6) The vinyl aromatic monomer preferably is selected from the group consisting of styrene, α-methyl styrene and vinyl toluene. The vinyl aromatic monomer more preferably is styrene.

(7) The alkylene preferably is selected from the group consisting of ethylene, propylene, butylene, pentene, hexane, octane, butadiene, isoprene, 1,3-pentadiene, 2,3-dimethyl-1,3-butadiene, pyperylene, 2,4-hexadiene, 3-butyl-1,3-octadiene and phenyl-1,3-butadiene. The alkylene more preferably is butadiene or isoprene.

(8) The thermoplastic elastomers of the present invention can be in the form of a linear diblock, triblock and multiblock copolymer or in the form of radial block copolymers. A mixture of linear and radial block copolymers can also be used according to the present invention.

(9) The soft blocks of the thermoplastic elastomer preferably contains a total alkylene monomer which is more than 50% a mole, preferably at least 70% mole, the remaining portion, if any, consisting of other copolymerizable monomers such as vinylaromatic monomers.

(10) The thermoplastic elastomer of the present invention preferably comprises between 10 and 70% by weight, more preferably between 10 and 60% by weight, most preferably between 20 and 50% by weight of hard blocks.

(11) The thermoplastic elastomer of the present invention preferably comprises of from 30 to 90% by weight, preferably of from 40 to 80% by weight, more preferably of from 50 to 70% by weight of at least one vinyl aromatic monomer.

(12) The hard blocks are characterized by a glass transition temperature which is higher than the service temperature; the soft blocks are characterized by a glass transition temperature which is lower than the service temperature and which is preferably comprised between 20 and −110° C., preferably between −10 and −100° C., more preferably between −20 and −90° C.

(13) The soft blocks of the thermoplastic elastomer may be partially or fully hydrogenated.

(14) The weight average molecular weight of the thermoplastic elastomer preferably ranges from 100,000 to 500,000 g/mole, more preferably from 150,000 to 400,000 g/mole.

(15) The thermoplastic elastomer of the present invention preferably is selected from the group consisting of styrene-butadiene-styrene, styrene-isoprene-styrene, styrene-isobutylene-styrene, styrene-ethylene-butylene-styrene and styrene-ethylene-propylene-styrene.

(16) The thermoplastic elastomer preferably is a styrene-butadiene-styrene block copolymer.

(17) Examples of thermoplastic elastomers suitable for being used in the blend of the present invention include Europrene (Polimeri Europe), Kraton (Kraton Performance Polymers Inc.), Stereon (Firestone Polymers), Styroflex (Styrolution), Finaprene (Total Petrochemicals), Tufprene (Asahi Kasei Corp) and Laprene and Soprene (So.F.Ter group).

(18) The thermoplastic polyurethane are obtained from reaction of a diisocyanate compound with at least one difunctional compound capable of reacting with an isocyanate group, preferably at least one difunctional hydroxyl group comprising compound and optionally a chain extender.

(19) The diisocyanate compound may be aromatic or aliphatic.

(20) Aromatic diisocyanates include, for example, 4,4′-, 2,2′- and 2,4′-methylene diphenyl diisocyanate and toluene diisocyanate; aliphatic diisocyanates include, for example, 1,6-hexamethylene diisocyanate, isophorone diisocyanate and 2,2′-, 4,4′- and 2,4′-dicyclohexylmethane diisocyanate. Mixtures of aromatic and aliphatic diisocyanates may be used.

(21) Preferred are isocyanate compositions comprising aromatic diisocyanates and more preferably methylene diphenyl diisocyanate.

(22) The difunctional compound capable of reacting with an isocyanate group preferably is a difunctional hydroxyl group comprising compound and may be selected from derivatives of polyesteramides, polythioethers, polycarbonates, polyacetals, polyolefins, polysiloxanes, polyesters, polyethers, polycaprolactone and mixtures thereof. Polyesters, polyethers, polycaprolactone are preferred.

(23) Suitable chain extenders include aliphatic diols such as 1,4-butanediol or 1,6-hexanediol or aminoalcohols such as N-methyldiethanolamine.

(24) The weight average molecular weight of the thermoplastic polyurethane preferably ranges from 50,000 to 400,000 g/mole, more preferably from 75,000 to 200,000 g/mole.

(25) Examples of thermoplastic polyurethanes suitable for being used in the blend of the present invention include Epamould (Epaflex Polyurethanes), Laripur (Coim S.p.A.), Apilon (Api Plastic S.p.A.), Estane and Pearlcoat/Pearlthane (Lubrizol), Avalon (Huntsman Polyurethanes), Elastollan (BASF) and Pellethane (Dow Chemical Co).

(26) The decorative surface coverings of the present invention are obtained from processing a composition comprising from 30 and 60% by weight, preferably from 35 to 55% by weight, more preferably from 40 to 50% by weight of the polymer blend comprising the above specified thermoplastic elastomer and thermoplastic polyurethane said polymer blend comprising between 40 and 80% by weight of thermoplastic polyurethane and between 60 and 20% by weight of thermoplastic elastomer. Preferably the polymer blend comprises between 50 and 70% by weight of thermoplastic polyurethane and between 50 and 30% by weight of thermoplastic elastomer.

(27) Preferred compositions according to the present invention further comprise ingredients such as lubricants, compatibilizers, silicones, antioxidants, fillers and pigments or dyes.

(28) Examples of suitable lubricants are of the stearic acid type, the fatty acid ester type, the fatty acid amide type, the paraffin hydrocarbon type, the napthenic hydrocarbon type, the metal soap type, the silicone type, polyethylene glycol type and waxes, used alone or as a mixture.

(29) Preferred lubricants include stearic acid and zinc stearate.

(30) Examples of suitable compatibilizers include ethylene/alkyl acrylate copolymers, ethylene/alkyl acrylate/carbon monoxide copolymers, ethylene/alkyl acrylate/carbon monoxide copolymers grafted with carboxylic acid anhydride groups, ethylene/alkyl acrylate/mono methyl maleate copolymers, ethylene/alkyl acrylate copolymers grafted with carboxylic acid anhydride groups, ethylene/vinyl acetate copolymers, ethylene/vinyl acetate copolymers grafted with carboxylic acid anhydride groups, ethylene/vinyl acetate/carbon monoxide copolymers; ethylene/vinyl acetate/carbon monoxide copolymers grafted with carboxylic acid anhydride groups and block copolymers comprising one or more alkylene(s) and one or more vinyl aromatic monomer(s) and grafted with carboxylic acid anhydride groups.

(31) Examples of silicones are polysiloxanes including polymers and copolymers comprising dimethylsiloxane units, methylhydrogensiloxane units, diphenylsiloxane units, phenylmethylsiloxane units, dimethylhydrogensiloxane units and trimethylsiloxane units.

(32) A preferred silicone is polydimethylsiloxane.

(33) Examples of suitable antioxidants include phenolic and thioester antioxidants. The antioxidants may be used alone or in combination. Preferred antioxidants are pentaerythritol tetrakis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate)(Irganox 1010) and octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate (Irganox 1076), both available from BASF.

(34) Examples of fillers suitable for the composition of the present invention can be any conventional filler, especially those types traditionally used in surface coverings.

(35) The filler can be organic, inorganic, or a combination of both, such as with different morphologies. Examples include, but are not limited to, coal fly ash, carbonate salts such as magnesium carbonate, calcium carbonate and calcium-magnesium carbonate, barium sulfate, carbon black, metal oxides, inorganic material, natural material, alumina trihydrate, magnesium hydroxide, bauxite, talc, mica, dolomite, barite, kaolin, silica, post-consumer glass, or post-industrial glass, synthetic and natural fiber, or any combination thereof.

(36) Preferably the filler comprises talc, mica, calcium carbonate, barite, kaolin, bauxite, dolomite, silica, glass, or any combination thereof.

(37) Examples of pigments and dyes suitable for the composition of the present invention are metallic oxides such as titanium dioxide, iron oxide, zinc oxide and the like, metal hydroxides, metal powders, sulphides, sulphates, carbonates, silicates, iron blues, organic reds, organic maroons and the like.

(38) The compositions according to the present invention can optionally contain one or more additives, such as, modifying resins, cross-linking agents, stabilizer, foaming agents, tackifiers, dispersion agents and/or other conventional organic or inorganic additives commonly used in polyolefin or in other surface coverings, such as, but not limited to, UV-stabilizers, antistatic agents, thermal and light stabilizers, flame retardants, or any combination thereof.

(39) Preferably the composition includes at least one pigment, flame retardant, thermal stabilizer, light stabilizer, antistatic agent, or any combination thereof.

(40) According to a first aspect of the present invention a decorative surface covering, more particularly floor and wall covering is provided.

(41) The decorative surface covering of the present invention comprises: from 25 and 70% by weight, preferably from 30 to 60% by weight, more preferably from 40 to 50% by weight of the polymer blend comprising one or more thermoplastic elastomer(s) and one or more thermoplastic polyurethane(s); from 2 to 8% by weight, preferably from 3 to 7% by weight, more preferably from 4 to 6% by weight of one or more compatibilizer(s); from 0.1 to 1.1% by weight, preferably from 0.3 to 0.9% by weight, more preferably from 0.5 to 0.7% by weight of one or more of the above lubricant(s); from 0.5 to 5% by weight, preferably from 1.5 to 4.5% by weight, more preferably from 2 to 4% by weight of one or more silicone(s); from 0.1 to 1% by weight, preferably from 0.15% to 0.7% by weight, more preferably from 0.2 to 0.5% by weight of one or more antioxidant(s); from 20 to 70% by weight, preferably from 30 to 60% by weight, more preferably from 40 to 50% by weight of one or more filler(s); from 0.1 to 10% by weight, preferably from 0.2 to 8% by weight, more preferably from 0.3 to 6% by weight of the one or more pigments and/or dyes; from 0 to 5% by weight, preferably from 0.1 to 4% by weight, more preferably from 0.3 to 5% by weight of the one or more additive(s),
based on the total weight of the composition.

(42) According to a second aspect of the present invention a method for producing said decorative surface coverings is provided.

(43) The method comprises: mixing the components of the composition, compounding the component-mix and providing a single coloured compound in strand form, repeating the mixing and compounding step for a plurality of compositions, wherein each of said compositions may be different.

(44) By a different composition the present invention means a composition differing from another composition by the type and the quantity of one or more ingredients (thermoplastic elastomer(s), thermoplastic polyurethane(s), compatibilizer(s), silicone(s), lubricant(s), antioxidant(s), filler(s), pigment(s), dye(s) and additive(s))

(45) The steps of mixing and compounding are repeated wherein different pigmentations result in a plurality of single coloured compounds in sheet form.

(46) Mixing generally is performed in a Banbury mixer, continuous mixer, a ribbon mixer or any combination thereof to form a blend.

(47) Compounding generally is performed in an extruder at a temperature comprised between 140 and 220° C., preferably between 150 and 200° C., more preferably between 160 and 190° C.

(48) A first embodiment of the method of the present invention comprises the further steps of: granulating each single coloured strand separately to form single coloured granules, scattering single coloured granules of different colour on a steel belt in a belt press, preferably a double belt press, or feeding them to a calender, converting the granules in a multi coloured sheet.

(49) A second embodiment of the method of the present invention comprises the further steps of: merging the plurality of single coloured strands by calendering to form a multilayer sheet, granulating the resulting multilayer sheet to form multi coloured granules, scattering multi coloured granules on a steel belt in a belt press, preferably a double belt press, or feeding them to a calender, converting the granules in a multi coloured sheet.

(50) A third embodiment of the method of the present invention comprises the further steps of: merging the plurality of single coloured strands by calendering to form a multi coloured marbled sheet, granulating the resulting multi coloured marbled sheet to form multi coloured marbled granules, scattering multi coloured marbled granules on a steel belt in a belt press, preferably a double belt press, or feeding them to a calender, converting the granules in a multi coloured sheet.

(51) A fourth embodiment of the method of the present invention comprises the further steps of: merging the plurality of single coloured strands by a granulating extruder to form multi coloured marbled granules, scattering multi coloured marbled granules on a steel belt in a belt press, preferably a double belt press, or feeding them to a calender, converting the granules in a multi coloured sheet.

(52) The calendering step, prior to the granulating step, is performed at a temperature comprised between 110 and 160° C., preferably between 120 and 150° C., more preferably between 130 and 140° C.

(53) The speed of the rollers in general is comprised between 2 and 15 m/min, preferably between 4 and 12 m/min, more preferably between 6 and 10 m/min.

(54) The granulating extruder step is performed at a temperature comprised between 40 and 150° C., preferably between 80 and 150° C., more preferably between 100 and 140° C. The speed of the screw in general is comprised between 10 and 30 rpm, preferably between 16 and 25 rpm, more preferably between 18 and 25 rpm.

(55) In each of the embodiments one to four, conversion of the granules into a multi coloured sheet is done under the following operation conditions: the temperature of the belt press or the calender is comprised between 130 and 220° C., preferably between 150 and 210° C., more preferably between 170 and 200° C., the speed of the belt press or the calender is comprised between 2 and 25 m/min, preferably between 10 and 18 m/min, more preferably between 12 and 16 m/min. the pressure of the belt press is comprised between 3 and 20 bar, preferably between 5 and 18 bar, more preferably between 8 and 15 bar,

(56) Further the method of the present invention comprises the additional step of providing a topcoat on the multi coloured sheet, wherein the topcoat is a cross-linked layer, preferably obtained by subjecting a radiation curable coating composition to actinic irradiation.

(57) The radiation curable coating composition in general comprises ethylenically unsaturated acrylic, ester, ether or urethane comprising polymers, oligomers or monomers and may be organic solvent free or water-borne.

(58) The process for contacting radiation curable coating composition with the multi-coloured marble sheet comprises any liquid coating application technique, known in the art, such as curtain coating, roller application or spray coating.

(59) The properties of the decorative surface coverings of the present invention are comparable or these of conventional PVC-based decorative surface coverings.

(60) On the other hand, the decorative surface coverings of the present invention have properties which are comparable to or superior than the currently existing PVC-free decorative surface coverings.

(61) The decorative surface coverings of the present invention can be produced on existing equipment intended for the production of PVC comprising surface coverings.

(62) They prove outstanding scratch and scuff resistance, form stability (creep) and are approved for wet room installations. They are easy to maintain and dry buff and is moreover easily recyclable due to the absence of a vulcanisation step.

EXAMPLES

(63) The following illustrative examples are merely meant to exemplify the present invention but is not destined to limit or otherwise define the scope of the present invention.

(64) The compositions, according to the formulation as given in table 1 to 5, were melt-mixed in an extruder at a temperature of about 170° C. delivering a single coloured compound in strand form.

(65) TABLE-US-00001 TABLE 1 Constituent % by weight Thermoplastic elastomer Calprene C-540 20.0 Thermoplastic polyurethane Pearlcoat 163K 25.0 Compatibilizer Fusabond N525 5.0 Filler Alrimal 447 S 44.0 Silicone Rhodorsil 30.000 3.0 Antioxidant Irganox 1010 0.3 Lubricant Ligastar ZN101/6 1.6 Pigment Titanium dioxide 1.1

(66) TABLE-US-00002 TABLE 2 Constituent % by weight Thermoplastic elastomer Europrene SOL T 6414 20.0 Thermoplastic polyurethane Elastollan 1185A10 20.0 Compatibilizer Kraton FG1901 10.0 Filler Afrimal 447 S 28.0 Myanit A10 10.0 Reasorb 90 6.0 Silicone Rhodorsil 30.000 3.0 Antioxidant Irganox 1076 0.3 Lubricant Ligastar ZN101/6 1.6 Pigment Titanium dioxide 1.1

(67) TABLE-US-00003 TABLE 3 Constituent % by weight Thermoplastic elastomer Finaclear 602 D 35.0 Thermoplastic polyurethane Pearlcoat 127K 10.0 Compatibilizer Kraton FG1901 5.0 Filler Martinal ON313 44.0 Silicone Rhodorsil 30.000 3.0 Antioxidant Irganox 1076 0.5 Lubricant Ligastar ZN101/6 1.4 Pigment Titanium dioxide 1.1

(68) TABLE-US-00004 TABLE 4 Constituent % by weight Thermoplastic elastomer Tufprene A 35.0 Thermoplastic polyurethane Pearlcoat 127K 10.0 Compatibilizer Fusabond C250 5.0 Filler Martinal OL104 LEO 44.0 Silicone Rhodorsil 30.000 3.0 Antioxidant Irganox 1010 0.5 Lubricant Ligastar ZN101/6 1.4 Pigment Titanium dioxide 1.1

(69) TABLE-US-00005 TABLE 5 Constituent % by weight Thermoplastic elastomer Calprene C-540 5.0 Thermoplastic polyurethane Pearlcoat 163K 40.0 Compatibilizer Kraton FG1901 5.0 Filler Afrimal 447 S 27.0 Myanit A10 10.0 Reasorb 90 7.0 Silicone Rhodorsil 30.000 3.0 Antioxidant Irganox 1076 0.5 Lubricant Ligastar ZN101/6 1.4 Pigment Titanium dioxide 1.1

(70) In these tables Calprene® C540 is a linear styrene/butadiene/styrene block copolymer from Dynasol; Europrene® SOL T6414 is a radial styrene butadiene block copolymer from Polimeri Europa; Finaclear® 602 D is a styrene/butadiene/styrene block copolymer from Total Petrochemicals; Tufprene® A is a styrene/butadiene block copolymers from Asahi Kasei; Pearlcoat® 163K is a polyether based thermoplastic polyurethane from Lubrizol; Pearlcoat®, 127K is a polyester-based thermoplastic polyurethane from Lubrizol; Elastollan 1185A 10 is an aromatic thermoplastic polyether polyurethane from BASF; Fusabond® N525 is an anhydride modified ethylene copolymer from Dupont; Fusabond® C250 is a modified ethylene vinyl acetate copolymer from Dupont; Kraton® FG1901 G is a linear triblock copolymer based on styrene and ethylene/butylene comprising maleic anhydride from Kraton; Afrimal 447 S is aluminumhydroxide from Alpha Calcit; Myanit A 10 is medium particle size dolomite from Omya; Reasorb 90 is calcium carbonate from Omya; Martinal ON 313 and Martinal® OL 104 LEO is aluminumhydroxide from Albemarle; Rhodorsi® 47 V30.000 is polydimethylsiloxane from Clearco Products; Irganox 1010 and Irganox 1076 is a sterically hindered phenolic antioxidant from Ciba Specialty Chemicals; Ligastar Zn 101/6 is zinc stearate from Peter Greven and titanium dioxide is from Sachtleben.

(71) For the respective compositions of table 1 to 5, except for the pigment (titanium dioxide), three strands of different colour, were prepared and subsequently granulated and calendered in a roller mill at a temperature of 134° C. and a roller speed of 10 m/min. to form marbled sheets 1 to 5.

(72) Each thus obtained sheet was then granulated to obtain multi coloured marbled granules of suitable sizes (e.g. 0.1 to 40 mm). The granules were scattered on the steel belt in a double belt press, wherein the double belt press operates at a temperature of 185° C., a pressure of 18 bar and a belt speed of 12 m/min., and pressed to a multi coloured, sheet.

(73) The respective multi coloured sheets 1 to 5, then were subjected to partially specific testing methods of the inventor that can be shortly described as follows:

(74) Scratch Resistance

(75) The apparatus with the scratching tool is placed over the sample so that a wagon can be pulled across the surface. The applied force starts with 0.5N and increase 0.5N each time until a scratch appears. The results are expressed as load (N) resulting in a scratch that can be seen (=visual) and load (N) resulting in a scratch that can be felt (feeling).

(76) Friction

(77) Friction is measured with a modified Tortus friction tester. Instead of using the measuring foot, a sled is fastened to the machine by a line. The force required to drag the sled over the surface of the sample with the motor of the machine is recorded as the friction value.

(78) Soiling and Cleaning

(79) A flooring sample is placed inside a drum with the wear surface exposed. A rubber-coated tetrahedron (or tetrapod) weight and a soiling compound are added and are tumbled as the drum rotates 1000 revolutions.

(80) After the soiling and scratching of the surface, loose dirt is wiped off by using a paper tissue.

(81) The test material is laid flat and fixed to the sample holders on the moving board of the cleaning device.

(82) The cleaning procedure simulates cleaning/washing by machine. The cleaning is carried out with a detergent dissolved in water. The rotating cleaning pad passes over the surface 6 times.

(83) The test results are visually evaluated by using a grey scale and ranked according to the degree of soiling and scratching. The results are described on a scale from 0 to 5, wherein 0 stands for severe damage while 5 stands for no visible change.

(84) Fire Retardance

(85) The fire retardance is based on the radiant panel test EN ISO 9239-1, wherein a test specimen is placed horizontally below a gas-fired radiant panel inclined at 30°. The specimen is exposed to a defined field of total heat flux, 11 kW/m2 at the hotter end close to the radiant panel, and decreasing to 1 kW/m2 at the other end farther away from the radiant panel.

(86) A pilot flame front from a line burner is applied to the hotter end in order to ignite the specimen.

(87) The progress of the flame front along the length of the specimen is recorded in terms of the time it takes to travel to various distances. The smoke development during the test is measured on the basis of light obscuration by smoke in the exhaust duct. The duration of the test is 30 minutes.

(88) The classification criterion is the critical heat flux (CHF) defined as the radiant flux at which the flame extinguishes or the radiant flux after a test period of 30 minutes, whichever is lower. In other words, CHF is the flux corresponding to the furthest extent of spread of flame.

(89) In this test BFL stands for a critical flux ≥8.0 kW.Math.m-2; CFL stands for a critical flux ≥4.5 kW.Math.m-2; DFL stands for a critical flux ≥3.0 kW.Math.m-2 and s1 stands for a smoke production ≤750%.Math.minutes.

(90) The test results for sheets 1 to 5, obtained from processing the compositions of table 1 to 5 respectively, are shown in table 6 and all are situated within the ranges as indicated in column 3 (Floor according to the invention)

(91) TABLE-US-00006 TABLE 6 Scratch Floor according Resistance Rubber Floor to the invention Demands Visual (N) 1 2.5-3   ≥2 Feeling (N) 2 4-5 ≥3 Friction 2.3-2.6 1.5-2.0 1.3-2 Soiling and 4 4-5   3 Cleaning Fire Retardance C.sub.FL s1 B.sub.FL s1 C.sub.FL s1
Dry Buffing

(92) In order to judge dry maintenance performance of a floor material evaluation of the result of dry buffing is very appropriate. Dry buffing is the most efficient method to use to restore the floor's surface once wear has become visible. As the pad of the dry buffing consists of non-woven fiber and resinous binder in which abrasive particles may or may not be distributed, frictional heat is produced by frictional rubbing of the pad on floor's surface, thus removing completely or partially most of the wear indicators. It is best to dry-buff right after the floor has been machine cleaned. Dry buffing limits renewed soiling. Best result is obtained by 500 to 1500 rpm and the use of a red pad.

(93) Dry buffing was performed using a high speed Clean Star D-430 buffing machine manufactured by Amano. Colour change, gloss, abrasion and blister on the surface layer were examined after one, two or three times of a 20 second dry buffing. The gloss of the floor material of the present invention was markedly increased with the number of polishing times. In addition, the procedure caused no changes in colour, generated no obvious abrasion and formed no blisters, thus showing the markedly excellent dry maintenance performance by a high speed buffing machine.

(94) The decorative floor coverings, processed from the compositions of the present invention, are characterized by an improved processability compared to rubber flooring: as a result of the absence of the vulcanisation step, a process characterized by more flexibility in process temperatures and melt viscosity is feasible. Because no vulcanisation is performed, the decorative surface coverings of the present invention are about 100% recyclable.