US3616138A - Carpet structure with foamed secondary backing - Google Patents

Carpet structure with foamed secondary backing Download PDF

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Publication number
US3616138A
US3616138A US871757*A US3616138DA US3616138A US 3616138 A US3616138 A US 3616138A US 3616138D A US3616138D A US 3616138DA US 3616138 A US3616138 A US 3616138A
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Prior art keywords
carpet
resin
foamed
adhesive
backing
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US871757*A
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Victor Harold Wentworth
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Monsanto Chemicals Ltd
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Monsanto Chemicals Ltd
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Classifications

    • DTEXTILES; PAPER
    • D05SEWING; EMBROIDERING; TUFTING
    • D05CEMBROIDERING; TUFTING
    • D05C17/00Embroidered or tufted products; Base fabrics specially adapted for embroidered work; Inserts for producing surface irregularities in embroidered products
    • D05C17/02Tufted products
    • D05C17/023Tufted products characterised by the base fabric
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N7/00Flexible sheet materials not otherwise provided for, e.g. textile threads, filaments, yarns or tow, glued on macromolecular material
    • D06N7/0063Floor covering on textile basis comprising a fibrous top layer being coated at the back with at least one polymer layer, e.g. carpets, rugs, synthetic turf
    • D06N7/0071Floor covering on textile basis comprising a fibrous top layer being coated at the back with at least one polymer layer, e.g. carpets, rugs, synthetic turf characterised by their backing, e.g. pre-coat, back coating, secondary backing, cushion backing
    • D06N7/0073Floor covering on textile basis comprising a fibrous top layer being coated at the back with at least one polymer layer, e.g. carpets, rugs, synthetic turf characterised by their backing, e.g. pre-coat, back coating, secondary backing, cushion backing the back coating or pre-coat being applied as an aqueous dispersion or latex
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N7/00Flexible sheet materials not otherwise provided for, e.g. textile threads, filaments, yarns or tow, glued on macromolecular material
    • D06N7/0063Floor covering on textile basis comprising a fibrous top layer being coated at the back with at least one polymer layer, e.g. carpets, rugs, synthetic turf
    • D06N7/0071Floor covering on textile basis comprising a fibrous top layer being coated at the back with at least one polymer layer, e.g. carpets, rugs, synthetic turf characterised by their backing, e.g. pre-coat, back coating, secondary backing, cushion backing
    • D06N7/0076Floor covering on textile basis comprising a fibrous top layer being coated at the back with at least one polymer layer, e.g. carpets, rugs, synthetic turf characterised by their backing, e.g. pre-coat, back coating, secondary backing, cushion backing the back coating or pre-coat being a thermoplastic material applied by, e.g. extrusion coating, powder coating or laminating a thermoplastic film
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N2203/00Macromolecular materials of the coating layers
    • D06N2203/04Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06N2203/042Polyolefin (co)polymers
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N2203/00Macromolecular materials of the coating layers
    • D06N2203/04Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06N2203/045Vinyl (co)polymers
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N2205/00Condition, form or state of the materials
    • D06N2205/04Foam
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/23907Pile or nap type surface or component
    • Y10T428/23986With coating, impregnation, or bond
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/23907Pile or nap type surface or component
    • Y10T428/23993Composition of pile or adhesive
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • Y10T428/249953Composite having voids in a component [e.g., porous, cellular, etc.]
    • Y10T428/249976Voids specified as closed
    • Y10T428/249977Specified thickness of void-containing component [absolute or relative], numerical cell dimension or density
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • Y10T428/249953Composite having voids in a component [e.g., porous, cellular, etc.]
    • Y10T428/249982With component specified as adhesive or bonding agent
    • Y10T428/249985Composition of adhesive or bonding component specified

Definitions

  • Sullivan ABSTRACT Carpets, particularly tufted carpets having a primary backing of hessian or jute, having a secondary backing which comprises an extruded foamed aliphatic thermoplastic resin having a glass transition temperature below ordinary room temperature.
  • the resin is an olefin polymer or copolymer, e.g., polyethylene, and the foamed resin has a predominantly closed cell structure, the majority of the cells having a diameter of 0002-01 inch.
  • the foamed resin can be up to 0.5-inch thick; can be in the form ofa continuous sheet, a woven fabric or net, or a plurality of adjacent sheets; and, if desired, can be perforated, corrugated, or embossed.
  • It can be fastened to the back of the carpet in any convenient manner, e.g., by sewing it in place or by adhering it by means ofa suita' ble adhesive such as a pressure-sensitive adhesive, a latex adhesive, or a heat-sensitive adhesive.
  • a suita' ble adhesive such as a pressure-sensitive adhesive, a latex adhesive, or a heat-sensitive adhesive.
  • This invention relates to carpets, and particularly tocarpets having a secondary backing.
  • the invention which comprises a carpet having a secondary backing comprising an extruded foamed aliphatic thermoplastic resin that has a glass-transition temperature below ordinary room temperature, is particularly applicable to tufted carpets which are not woven in the traditional way but comprise individual tufts of pile yarn pulled through a primary backing fabric, normally of jute or hessian, and anchored in place by means of a binding composition.
  • Binding compositions can for example be those described in British Patent specifications Nos. 903,009 and 969,368.
  • more conventional carpets for example Wilton or Axminster, can usefully have applied to them a secondary backing according to the invention.
  • the aliphatic thermoplastic resin is one derived by polymerization or copolymerization of an ethylenically unsaturated monomer.
  • the monomer is preferably an ethylenically unsaturated hydrocarbon, and more specifically an olefin, but it may for instance be a nitrile, such as acrylonitrile; vinyl or vinylidene chloride, vinyl acetate, or an acrylate, such as ethyl acrylate or methyl methacrylate.
  • the most suitable hydrocarbon monomers are ethylene, propylene, and the butylenes.
  • the polymer may be polyethylene (lowdensity or high-density material) or polypropylene.
  • copolymers of at least 50 percent by weight of the ethylenically unsaturated monomers mentioned above, with up to 50 percent by weight of other ethylenically unsaturated monomers copolymerizable therewith, such as maleates, fumarates, divinyl benzene, divinyl phthalate, diallyl maleate, etc. may be employed in the practice of this invention.
  • a copolymer of one of the hydrocarbon monomers (such as ethylene) with another ethylenically unsaturated monomer, such as one of those given above is employed.
  • the copolymer can, for example, be an ethylene-vinyl acetate copolymer.
  • the resin has a glass-transition temperature below ordinary room temperature.
  • the glass-transition temperature of a resin sometimes known as its second-order transition temperature, is defined as the temperature below which the resin is hard and rigid but above which it possesses elastic properties.
  • glass-transition temperature is thus normally below about 20" C., and preferably below C.
  • resins derived by polymerization or copolymerization of the monomers mentioned above for example polyethylene, intrinsically possess glass-transition temperatures below room temperature, but others, for example, polyvinyl chloride, may require the addition of a plasticizer in order to achieve a sufficiently low glasstransition temperature.
  • plasticizers include, for example, dioctyl phthalate and chlorinated diphenyl.
  • the resin is in the form of an extruded foam, which can be made by extruding a foamable resin composition containing a blowing agent.
  • the blowing agent is preferably a normally gaseous substance but it can be a volatile liquid. in many cases the blowing agent is one that is normally gaseous but which while under pressure before extrusion is present in the liquid state.
  • volatile substances include lower aliphatic hydrocarbons, such as: ethane, propane, a butane or butene, or a pentane or pentene; lower alkyd halides, such as methyl chloride, trichloromethane or 1,2- dichlorotetrafluoroethane; and inorganic gases such as carbon dioxide or nitrogen.
  • the lower aliphatic hydrocarbons especially a butane, or mixture of butanes
  • the blowing agent can also be a chemical blowing agent, which can for example be a bicarbonate such as for example sodium bicarbonate or ammonium bicarbonate, or an organic nitrogen compound that yields nitrogen on heating, such as for example dinitrosopentamethylenediamine or barium azodicarboxylate.
  • a bicarbonate such as for example sodium bicarbonate or ammonium bicarbonate
  • an organic nitrogen compound that yields nitrogen on heating such as for example dinitrosopentamethylenediamine or barium azodicarboxylate.
  • From 3 to 30 percent, especially 7 to'20 percent, by weight based on the weight of the resin is generally a suitable proportion of blowing agent.
  • the use of from 7to l5percent by weight of butane in conjunction with polyethylene has given excellent results.
  • the foamable resin contains a nucleating agent, which assists in the formation of a large number of small cells.
  • a nucleating agent which assists in the formation of a large number of small cells.
  • nucleating agents can be employed, including finely divided inert solids such as for example silica or alumina, preferably in conjunction with zinc stearate, or small quantities of a substance that decomposes at the extrusion temperature to give a gas.
  • An example of the latter class of nucleating agents is sodium bicarbonate, used if desired in conjunction with a weak acid such as tartaric acid or citric acid.
  • a small proportion of the nucleating agent for example up to 5 percent by weight of the resin, is usually effective.
  • Extrusion of the resin takes place through a die, which is normally of the slit type so that a sheet of resin is produced.
  • Slit dies that have modified so as to produce a more uniform product, as described in British Patent specifications 1,034,120 and 1,089,561 can often be advantageously used.
  • the density of the foamed resin may vary between fairly wide limits. Foamed resins having a density between 1 pound per cubic foot or slightly less and l0 pound per cubic foot or more are suitable. Resins having a density between 1 and 7 pounds per cubic foot, and preferably between 2 and 4 pounds per cubic foot, are generally most useful, particularly in the case of a foamed polyethylene.
  • thefoamed resin has a predominantly closed cell structure, the majority of the cells may for example have a diameter of from 0.002 to 0.1 inch. Preferably the majority of the cells have a diameter offrom 0.003 to 0.01 inch.
  • the foamed resin may be in the form; of a continuous sheet, perforated by a number of holes about 0.l inch in diameter and spaced about 0.25 inch apart, or it can be a woven fabric or net comprising strands of the extruded foamed resin. Alternatively, a number of strips of foamed resin can be used side by side, and the resin can be corrugated or embossed.
  • a very suitable form of foamed resin is that described in British Patent specification No. 1,089,561.
  • the foamed resin may be up to 0.5-in.cl1 thick. Usually however, it will be in the range of about 0.05 inch to 0.3-inch thick. Preferably, the thickness is from 0.! inch to 0.25 inch.
  • the foamed resin may be fastened to the carpet in any convenient way.
  • a suitable adhesive for instance an "impact" or pressure-sensitive adhesive, or one that comprises a polymer latex, especially a latex of a natural or synthetic rubber such as a styrene/butadiene rubber or a nitrile rubber.
  • a mineral filler such as barytes, china clay, whiting or titanium dioxide may also be present. Excellent results can often be obtained using as adhesive a composition comprising a latex and a filler of the kind that are commonly applied as a binding composition to a primary backing of tufted carpets.
  • the foamed resin secondary backing can conveniently be applied to the partially dried binding composition on the primary backing, thus eliminating the need for additional adhesive.
  • the adhesive or binding composition is dried out. Drying is facilitated if the foamed resin is perforated as mentioned above. Good results are obtainable by applying a heat-sensitive adhesive such as polyvinyl acetate to the foamed resin and then placing the treated resin against the back of the carpet while the latter is hot, for example from a drying operation.
  • the first carpet was a tufted one comprising tufts of rayon pulled through a hessian primary backing fabric and anchored in place by a binding composition comprising a styrenebutadiene copolymer containing 60 percent by weight of combined styrene together with whiting as a filler.
  • the secondary backing consisted of strips of foamed polyethylene having a density of 2 pounds per cubic foot, containing predominantly closed cells of diameter about 0.040 inch.
  • the strips were 0.125 inch thick and 8 inches wide and were made by extruding a foamable polyethylene composition containing 3 percent by weight of finely divided silica, l percent by weight of zinc stearat'e and 10 percent by weight of butane through a slit orifice of length 2 inches, a width 0.040 inches and a land 0.75 inch.
  • the secondary backing was stuck to the back of the carpet by means of a commercial adhesive of the impact type, a thin layer of adhesive being spread on the back of the carpet and on the secondary backing and allowed to dry for minutes, and the two surfaces then being pressed firmly together.
  • Example I was repeated using strips of foamed ethylene vinyl acetate copolymer wherein the copolymer had a vinyl acetate content of 35 percent.
  • EXAMPLE Vll Examples 1 and II were repeated except that the polyethylene was applied to the primary backing in the form of a perforated continuous sheet.
  • the improvement which comprises a secondary backing sheet adhered thereto; said secondary backing sheet comprising an extruded foamed aliphatic thermoplastic resin; said resin having a glass-transition temperature below ordinary room temperature; said secondary backing sheet having a multiplicity of voids extending therethrough from one face of the sheet to the other and being a woven fabric comprising strands of the extruded foamed aliphatic thermoplastic resin, said voids being formed by the interstices of the weave.
  • the improved carpet of claim 1 wherein the carpet is a tufted carpet comprising individual tufts of pile yarn pulled through a primary backing fabric.

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Carpets (AREA)
  • Laminated Bodies (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

Carpets, particularly tufted carpets having a primary backing of hessian or jute, having a secondary backing which comprises an extruded foamed aliphatic thermoplastic resin having a glass transition temperature below ordinary room temperature. Preferably, the resin is an olefin polymer or copolymer, e.g., polyethylene, and the foamed resin has a predominantly closed cell structure, the majority of the cells having a diameter of 0.002-0.1 inch. The foamed resin can be up to 0.5-inch thick; can be in the form of a continuous sheet, a woven fabric or net, or a plurality of adjacent sheets; and, if desired, can be perforated, corrugated, or embossed. It can be fastened to the back of the carpet in any convenient manner, e.g., by sewing it in place or by adhering it by means of a suitable adhesive such as a pressure-sensitive adhesive, a latex adhesive, or a heatsensitive adhesive.

Description

United States Patent [72] Inventor Victor Harold Wentworth Uxbridge, England [21] Appl. No, 871,757 [22] Filed Aug. 12, 1969 [45] Patented Oct. 26, 1971 [73] Assignee Monsanto Chemicals Limited London, England [3 2] Priority Nov. 23, 1964 [3 3] Great Britain [31 47,533/64 Continuation of application Ser. No. 506,400, Nov. 4, 1965, now abandoned.
[54] CARPET STRUCTURE WITH FOAMED SECONDARY BACKING 5 Claims, No Drawings [52] U.S.C1 161/67, 161/112, 161/143, 161/159 [51] Int. Cl D05c 17/02 [50] Field of Search 161/62-67, 109, 112,113, 159-161; 156/72 [5 6] References Cited UNITED STATES PATENTS 2,312,200 2/1943 Teague et a1. 161/76 3,100,926 8/1963 Richmond 264/45 Primary ExaminerRobert F. Burnett Assistant Examiner-Linda M. Carlin Attorneys-Herbert B. Roberts, Arthur S. Hoffman and Paul E. Sullivan ABSTRACT: Carpets, particularly tufted carpets having a primary backing of hessian or jute, having a secondary backing which comprises an extruded foamed aliphatic thermoplastic resin having a glass transition temperature below ordinary room temperature. Preferably, the resin is an olefin polymer or copolymer, e.g., polyethylene, and the foamed resin has a predominantly closed cell structure, the majority of the cells having a diameter of 0002-01 inch. The foamed resin can be up to 0.5-inch thick; can be in the form ofa continuous sheet, a woven fabric or net, or a plurality of adjacent sheets; and, if desired, can be perforated, corrugated, or embossed. It can be fastened to the back of the carpet in any convenient manner, e.g., by sewing it in place or by adhering it by means ofa suita' ble adhesive such as a pressure-sensitive adhesive, a latex adhesive, or a heat-sensitive adhesive.
CARPET STRUCTURE WITH FOAMED SECONDARY BACKING This application is a continuation of copending application Ser. No. 506,400, filed Nov. 4, 1965 and now abandoned.
This invention relates to carpets, and particularly tocarpets having a secondary backing.
It has been proposed to apply to carpets, particularly those of the tufted type, a secondary backing consisting of hessian fabric in order to improve the appearance and provide additional stiffness for the carpet as a whole. A secondary backing of hessian has been found to have some disadvantages, how ever, including the serious one that it can make the carpet more likely to slip on polished floors.
It is therefore an object of this invention to provide an improved backing for carpets and the like.
It is a further object of this invention to provide an improved carpet having a secondary backing comprising an extruded foamed aliphatic thermoplastic resin having a glasstransition temperature below ordinary room temperature.
Each of the above objects has been realized through the development of a new type of secondary backing that not only improves the appearance and handle of the carpet, but also increases its resilience, resistance to wear and apparent depth and is moreover less likely than hessian to slip on floor surfaces.
The invention, which comprises a carpet having a secondary backing comprising an extruded foamed aliphatic thermoplastic resin that has a glass-transition temperature below ordinary room temperature, is particularly applicable to tufted carpets which are not woven in the traditional way but comprise individual tufts of pile yarn pulled through a primary backing fabric, normally of jute or hessian, and anchored in place by means of a binding composition. Binding compositions can for example be those described in British Patent specifications Nos. 903,009 and 969,368. However, more conventional carpets, for example Wilton or Axminster, can usefully have applied to them a secondary backing according to the invention.
The aliphatic thermoplastic resin is one derived by polymerization or copolymerization of an ethylenically unsaturated monomer. The monomer is preferably an ethylenically unsaturated hydrocarbon, and more specifically an olefin, but it may for instance be a nitrile, such as acrylonitrile; vinyl or vinylidene chloride, vinyl acetate, or an acrylate, such as ethyl acrylate or methyl methacrylate. The most suitable hydrocarbon monomers are ethylene, propylene, and the butylenes. For instance, the polymer may be polyethylene (lowdensity or high-density material) or polypropylene. Moreover, copolymers of at least 50 percent by weight of the ethylenically unsaturated monomers mentioned above, with up to 50 percent by weight of other ethylenically unsaturated monomers copolymerizable therewith, such as maleates, fumarates, divinyl benzene, divinyl phthalate, diallyl maleate, etc., may be employed in the practice of this invention. Preferably, a copolymer of one of the hydrocarbon monomers (such as ethylene) with another ethylenically unsaturated monomer, such as one of those given above is employed. Thus, the copolymer can, for example, be an ethylene-vinyl acetate copolymer.
The resin has a glass-transition temperature below ordinary room temperature. The glass-transition temperature of a resin, sometimes known as its second-order transition temperature, is defined as the temperature below which the resin is hard and rigid but above which it possesses elastic properties. The
glass-transition temperature is thus normally below about 20" C., and preferably below C. Many of the resins derived by polymerization or copolymerization of the monomers mentioned above, for example polyethylene, intrinsically possess glass-transition temperatures below room temperature, but others, for example, polyvinyl chloride, may require the addition of a plasticizer in order to achieve a sufficiently low glasstransition temperature. Suitable plasticizers include, for example, dioctyl phthalate and chlorinated diphenyl.
The resin is in the form of an extruded foam, which can be made by extruding a foamable resin composition containing a blowing agent. The blowing agent is preferably a normally gaseous substance but it can be a volatile liquid. in many cases the blowing agent is one that is normally gaseous but which while under pressure before extrusion is present in the liquid state. Examples of volatile substances that can be used include lower aliphatic hydrocarbons, such as: ethane, propane, a butane or butene, or a pentane or pentene; lower alkyd halides, such as methyl chloride, trichloromethane or 1,2- dichlorotetrafluoroethane; and inorganic gases such as carbon dioxide or nitrogen. The lower aliphatic hydrocarbons, especially a butane, or mixture of butanes, are preferred. The blowing agent can also be a chemical blowing agent, which can for example be a bicarbonate such as for example sodium bicarbonate or ammonium bicarbonate, or an organic nitrogen compound that yields nitrogen on heating, such as for example dinitrosopentamethylenediamine or barium azodicarboxylate. From 3 to 30 percent, especially 7 to'20 percent, by weight based on the weight of the resin is generally a suitable proportion of blowing agent. For example, the use of from 7to l5percent by weight of butane in conjunction with polyethylene has given excellent results.
Preferably the foamable resin contains a nucleating agent, which assists in the formation of a large number of small cells. A wide range of nucleating agents can be employed, including finely divided inert solids such as for example silica or alumina, preferably in conjunction with zinc stearate, or small quantities of a substance that decomposes at the extrusion temperature to give a gas. An example of the latter class of nucleating agents is sodium bicarbonate, used if desired in conjunction with a weak acid such as tartaric acid or citric acid. A small proportion of the nucleating agent, for example up to 5 percent by weight of the resin, is usually effective.
Extrusion of the resin takes place through a die, which is normally of the slit type so that a sheet of resin is produced. Slit dies that have modified so as to produce a more uniform product, as described in British Patent specifications 1,034,120 and 1,089,561 can often be advantageously used.
The density of the foamed resin may vary between fairly wide limits. Foamed resins having a density between 1 pound per cubic foot or slightly less and l0 pound per cubic foot or more are suitable. Resins having a density between 1 and 7 pounds per cubic foot, and preferably between 2 and 4 pounds per cubic foot, are generally most useful, particularly in the case of a foamed polyethylene.
Preferably thefoamed resin has a predominantly closed cell structure, the majority of the cells may for example have a diameter of from 0.002 to 0.1 inch. Preferably the majority of the cells have a diameter offrom 0.003 to 0.01 inch.
The foamed resin may be in the form; of a continuous sheet, perforated by a number of holes about 0.l inch in diameter and spaced about 0.25 inch apart, or it can be a woven fabric or net comprising strands of the extruded foamed resin. Alternatively, a number of strips of foamed resin can be used side by side, and the resin can be corrugated or embossed.
A very suitable form of foamed resin is that described in British Patent specification No. 1,089,561.
The foamed resin may be up to 0.5-in.cl1 thick. Usually however, it will be in the range of about 0.05 inch to 0.3-inch thick. Preferably, the thickness is from 0.! inch to 0.25 inch.
The foamed resin may be fastened to the carpet in any convenient way. For example, it may be sewn in place or stuck to the back of the carpet by means of a suitable adhesive, for instance an "impact" or pressure-sensitive adhesive, or one that comprises a polymer latex, especially a latex of a natural or synthetic rubber such as a styrene/butadiene rubber or a nitrile rubber. A mineral filler such as barytes, china clay, whiting or titanium dioxide may also be present. Excellent results can often be obtained using as adhesive a composition comprising a latex and a filler of the kind that are commonly applied as a binding composition to a primary backing of tufted carpets. Where the carpet tufted, the foamed resin secondary backing can conveniently be applied to the partially dried binding composition on the primary backing, thus eliminating the need for additional adhesive. After the foamed resin is applied to the carpet the adhesive or binding composition is dried out. Drying is facilitated if the foamed resin is perforated as mentioned above. Good results are obtainable by applying a heat-sensitive adhesive such as polyvinyl acetate to the foamed resin and then placing the treated resin against the back of the carpet while the latter is hot, for example from a drying operation.
The invention is illustrated by the following Examples.
EXAMPLE I This example describes the production of carpets having a secondary backing according to the invention.
The first carpet was a tufted one comprising tufts of rayon pulled through a hessian primary backing fabric and anchored in place by a binding composition comprising a styrenebutadiene copolymer containing 60 percent by weight of combined styrene together with whiting as a filler.
The secondary backing consisted of strips of foamed polyethylene having a density of 2 pounds per cubic foot, containing predominantly closed cells of diameter about 0.040 inch. The strips were 0.125 inch thick and 8 inches wide and were made by extruding a foamable polyethylene composition containing 3 percent by weight of finely divided silica, l percent by weight of zinc stearat'e and 10 percent by weight of butane through a slit orifice of length 2 inches, a width 0.040 inches and a land 0.75 inch.
The secondary backing was stuck to the back of the carpet by means of a commercial adhesive of the impact type, a thin layer of adhesive being spread on the back of the carpet and on the secondary backing and allowed to dry for minutes, and the two surfaces then being pressed firmly together.
A good bond was obtained and the carpet as a whole had an excellent handle and resilience. When laid on a floor the apparent depth and the resistance to wear and slipping were improved compared with those of a similar carpet having a secondary backing of hessian.
EXAMPLE II The same foamed resin secondary backing was applied in the same way to an Axminster woven carpet, and the same advantages were obtained.
EXAMPLE [11 Example I was repeated using strips of foamed ethylene vinyl acetate copolymer wherein the copolymer had a vinyl acetate content of 35 percent.
EXAMPLE lV Example I was repeated using foamed polyvinyl chloride resin having incorporated therein 50 parts of dioctyl phthalate.
EXAMPLE V Example I was repeated using foamed polyisobutylene in place of foamed polyethylene.
EXAMPLE Vl Example I was repeated using a foamed ethyl acrylate copolymer.
EXAMPLE Vll Examples 1 and II were repeated except that the polyethylene was applied to the primary backing in the form of a perforated continuous sheet.
The above description and particularly the examples are set forth for pu oses of illustration only. Magi; modifications and variations WI 1 be apparent to those skill in the art and can be made without departing from the scope of the invention herein described.
What is claimed is:
1. In combination with a carpet having a primary backing. the improvement which comprises a secondary backing sheet adhered thereto; said secondary backing sheet comprising an extruded foamed aliphatic thermoplastic resin; said resin having a glass-transition temperature below ordinary room temperature; said secondary backing sheet having a multiplicity of voids extending therethrough from one face of the sheet to the other and being a woven fabric comprising strands of the extruded foamed aliphatic thermoplastic resin, said voids being formed by the interstices of the weave.
2. The improved carpet of claim 1 wherein the carpet is a tufted carpet comprising individual tufts of pile yarn pulled through a primary backing fabric.
3. The improved carpet of claim 1 wherein the extruded foamed aliphatic thermoplastic resin is polyethylene.
4. The improved carpet of claim 1 wherein adhesion of the secondary backing sheet to the primary carpet backing is accomplished by means of a pressure-sensitive adhesive.
5. The improved carpet of claim 1 wherein adhesion of the secondary backing sheet to the primary carpet backing is accomplished by means of a heat-sensitive polyvinyl acetate adhesive.
i i i I i

Claims (4)

  1. 2. The improved carpet of claim 1 wherein the carpet is a tufted carpet comprising individual tufts of pile yarn pulled through a primary backing fabric.
  2. 3. The improved carpet of claim 1 wherein the extruded foamed aliphatic thermoplastic resin is polyethylene.
  3. 4. The improved carpet of claim 1 wherein adhesion of the secondary backing sheet to the primary carpet backing is accomplished by means of a pressure-sensitive adhesive.
  4. 5. The improved carpet of claim 1 wherein adhesion of the secondary backing sheet to the primary carpet backing is accomplished by means of a heat-sensitive polyvinyl acetate adhesive.
US871757*A 1964-11-23 1969-08-12 Carpet structure with foamed secondary backing Expired - Lifetime US3616138A (en)

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Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3975562A (en) * 1974-02-08 1976-08-17 Veb Leuna-Werke "Walter Ulbricht" Textile floor covering with bottom of thermoplastic foam and a method of producing it
US4199639A (en) * 1977-07-25 1980-04-22 Walter Ronc Sandwich-structured double layer floor covering
US4412877A (en) * 1981-04-06 1983-11-01 E. I. Du Pont De Nemours & Co. Embossing secondary backings of carpets
US4529639A (en) * 1984-06-27 1985-07-16 Collins & Aikman Corporation Molded foam-backed carpet assembly and method of producing same
US4579764A (en) * 1984-06-27 1986-04-01 Collins & Aikman Corporation Molded carpet assembly with sound deadening foam backing
USRE34951E (en) * 1986-08-29 1995-05-23 Interface, Inc. Flame retardant tufted carpet tile and method of preparing same
US5560972A (en) * 1988-07-25 1996-10-01 Interface, Inc. Latex fusion bonded pile carpets and carpet tile
WO1999025231A1 (en) * 1997-11-17 1999-05-27 Kanter Ray D Shock absorbing carpet system
US20020132085A1 (en) * 2000-11-24 2002-09-19 Higgins Kenneth B. Textile product and method
US20030161990A1 (en) * 2001-07-20 2003-08-28 Higgins Kenneth B. Residential carpet product and method
US20030170420A1 (en) * 2001-07-20 2003-09-11 Higgins Kenneth B. Residential carpet product and method
US20030219570A1 (en) * 2000-07-17 2003-11-27 Kanter Ray D. Shock absorbing carpet system
US6838147B2 (en) 1998-01-12 2005-01-04 Mannington Mills, Inc. Surface covering backing containing polymeric microspheres and processes of making the same
US20060134374A1 (en) * 2004-12-16 2006-06-22 Mohawk Carpet Corporation Vinyl polymer adhesives with post-consumer recycled glass powder filler
US7182989B2 (en) 2002-07-31 2007-02-27 Milliken & Company Flooring system and method
US20100258334A1 (en) * 2009-04-10 2010-10-14 Toyota Boshoku Kabushiki Kaisha Skin material of vehicle interior equipment and manufacturing method for the same
WO2016113025A1 (en) * 2015-01-12 2016-07-21 Protektorwerk Florenz Maisch Gmbh & Co. Kg Method, sewing device, and combined extruding and sewing device for sewing woven fabric to an extrudate

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1560722A1 (en) * 1966-11-17 1970-09-17 Gundernhausen Chemie Process for the production of floor covering with a non-slip covering back
GB1366703A (en) * 1971-06-04 1974-09-11 Monsanto Ltd Foamed resin laminates
US5204155A (en) * 1991-11-12 1993-04-20 Interface, Inc. Resilient foam-backed carpet and method of preparation

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3975562A (en) * 1974-02-08 1976-08-17 Veb Leuna-Werke "Walter Ulbricht" Textile floor covering with bottom of thermoplastic foam and a method of producing it
US4199639A (en) * 1977-07-25 1980-04-22 Walter Ronc Sandwich-structured double layer floor covering
US4412877A (en) * 1981-04-06 1983-11-01 E. I. Du Pont De Nemours & Co. Embossing secondary backings of carpets
US4529639A (en) * 1984-06-27 1985-07-16 Collins & Aikman Corporation Molded foam-backed carpet assembly and method of producing same
US4579764A (en) * 1984-06-27 1986-04-01 Collins & Aikman Corporation Molded carpet assembly with sound deadening foam backing
USRE34951E (en) * 1986-08-29 1995-05-23 Interface, Inc. Flame retardant tufted carpet tile and method of preparing same
US5560972A (en) * 1988-07-25 1996-10-01 Interface, Inc. Latex fusion bonded pile carpets and carpet tile
US6572952B1 (en) * 1997-11-17 2003-06-03 Ray D. Kanter Shock absorbing carpet system
WO1999025231A1 (en) * 1997-11-17 1999-05-27 Kanter Ray D Shock absorbing carpet system
US6090462A (en) * 1997-11-17 2000-07-18 Kanter; Ray D. Shock absorbing carpet system
US6838147B2 (en) 1998-01-12 2005-01-04 Mannington Mills, Inc. Surface covering backing containing polymeric microspheres and processes of making the same
US20030219570A1 (en) * 2000-07-17 2003-11-27 Kanter Ray D. Shock absorbing carpet system
US20020132085A1 (en) * 2000-11-24 2002-09-19 Higgins Kenneth B. Textile product and method
US20030161990A1 (en) * 2001-07-20 2003-08-28 Higgins Kenneth B. Residential carpet product and method
US20030170420A1 (en) * 2001-07-20 2003-09-11 Higgins Kenneth B. Residential carpet product and method
US7182989B2 (en) 2002-07-31 2007-02-27 Milliken & Company Flooring system and method
US20060134374A1 (en) * 2004-12-16 2006-06-22 Mohawk Carpet Corporation Vinyl polymer adhesives with post-consumer recycled glass powder filler
US20100258334A1 (en) * 2009-04-10 2010-10-14 Toyota Boshoku Kabushiki Kaisha Skin material of vehicle interior equipment and manufacturing method for the same
US8516697B2 (en) 2009-04-10 2013-08-27 Toyota Boshoku Kabushiki Kaisha Skin material of vehicle interior equipment and manufacturing method for the same
US8524622B2 (en) * 2009-04-10 2013-09-03 Toyota Boshoku Kabushiki Kaisha Skin material of vehicle interior equipment and manufacturing method for the same
WO2016113025A1 (en) * 2015-01-12 2016-07-21 Protektorwerk Florenz Maisch Gmbh & Co. Kg Method, sewing device, and combined extruding and sewing device for sewing woven fabric to an extrudate

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GB1089563A (en) 1967-11-01
FR1468932A (en) 1967-02-10

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