EP0003965B1 - Resinous polymer sheet materials having selective, surface decorative effects and methods of making the same - Google Patents

Resinous polymer sheet materials having selective, surface decorative effects and methods of making the same Download PDF

Info

Publication number
EP0003965B1
EP0003965B1 EP79100313A EP79100313A EP0003965B1 EP 0003965 B1 EP0003965 B1 EP 0003965B1 EP 79100313 A EP79100313 A EP 79100313A EP 79100313 A EP79100313 A EP 79100313A EP 0003965 B1 EP0003965 B1 EP 0003965B1
Authority
EP
European Patent Office
Prior art keywords
cross
wear layer
blowing
resinous polymer
polymerization initiator
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
EP79100313A
Other languages
German (de)
English (en)
French (fr)
Other versions
EP0003965A1 (en
Inventor
Harry Anthony Shortway
Alan Albert Graham
Charles Halisher Miller
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Congoleum Corp
Original Assignee
Congoleum Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Congoleum Corp filed Critical Congoleum Corp
Publication of EP0003965A1 publication Critical patent/EP0003965A1/en
Application granted granted Critical
Publication of EP0003965B1 publication Critical patent/EP0003965B1/en
Expired legal-status Critical Current

Links

Images

Classifications

    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, 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
    • D06N7/00—Flexible sheet materials not otherwise provided for, e.g. textile threads, filaments, yarns or tow, glued on macromolecular material
    • D06N7/0005—Floor covering on textile basis comprising a fibrous substrate being coated with at least one layer of a polymer on the top surface
    • D06N7/0007—Floor covering on textile basis comprising a fibrous substrate being coated with at least one layer of a polymer on the top surface characterised by their relief structure
    • D06N7/0013—Floor covering on textile basis comprising a fibrous substrate being coated with at least one layer of a polymer on the top surface characterised by their relief structure obtained by chemical embossing (chemisches Prägen)
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B44—DECORATIVE ARTS
    • B44C—PRODUCING DECORATIVE EFFECTS; MOSAICS; TARSIA WORK; PAPERHANGING
    • B44C1/00—Processes, not specifically provided for elsewhere, for producing decorative surface effects
    • B44C1/20—Applying plastic materials and superficially modelling the surface of these materials
    • B44C1/205—Applying plastic materials and superficially modelling the surface of these materials chemical modelling
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B44—DECORATIVE ARTS
    • B44C—PRODUCING DECORATIVE EFFECTS; MOSAICS; TARSIA WORK; PAPERHANGING
    • B44C1/00—Processes, not specifically provided for elsewhere, for producing decorative surface effects
    • B44C1/24—Pressing or stamping ornamental designs on surfaces
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, 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
    • D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/04—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06N3/06—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds with polyvinylchloride or its copolymerisation products
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, 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
    • D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/04—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06N3/06—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds with polyvinylchloride or its copolymerisation products
    • D06N3/08—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds with polyvinylchloride or its copolymerisation products with a finishing layer consisting of polyacrylates, polyamides or polyurethanes or polyester
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, 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
    • D06N7/00—Flexible sheet materials not otherwise provided for, e.g. textile threads, filaments, yarns or tow, glued on macromolecular material
    • D06N7/0005—Floor covering on textile basis comprising a fibrous substrate being coated with at least one layer of a polymer on the top surface
    • D06N7/0007—Floor covering on textile basis comprising a fibrous substrate being coated with at least one layer of a polymer on the top surface characterised by their relief structure
    • D06N7/001—Floor covering on textile basis comprising a fibrous substrate being coated with at least one layer of a polymer on the top surface characterised by their relief structure obtained by mechanical embossing

Definitions

  • the present invention relates to decorative sheet materials, and more particularly to decorative resinous polymer sheet materials having controlled, selective placement of surface decorative effects of use as floor, wall and ceiling coverings; desk, table and counter tops; surface layers on leather, fabrics, wood, paper, paper products, glass, metals, plastics, etc.; upholstery, drapery, clothing and apparel materials; interiors for cars, trucks, trains, airplanes, and other vehicles or other means of transportation; covers for books, periodicals and other publications; boxes, cartons, containers, and other receptacles; maps, road markers and similar and like articles.
  • the present invention is concerned with resinous polymer decorative sheet materials having smooth, glossy or lustrous surfaces in some areas; or embossed, dead or dull mat surfaces in other areas; or embossed, glossy or lustrous surfaces in still other areas; or smooth, dead and dull mat surfaces in still other areas; all of such areas sharply contrasting with each other and in perfect registry with a pattern or design printed on such decorative sheet materials.
  • Decorative sheet materials of a resinous polymer composition have been manufactured for many years and one of the commonest means of creating or enhancing the decorative effects has been to provide selected portions of the surface of such decorative sheet materials with different types of contrasting finishes or effects, or surface gloss or luster differentials, for example, with smooth, glossy or lustrous surfaces; embossed, dead or dull mat surfaces; embossed, glossy or lustrous; and smooth, dead or dull mat surfaces, all sharply contrasting with one another.
  • differential mechanical embossing inlaying or chemical etching, and other methods
  • differential mechanical embossing combined with pattern or design printing has always created registration problems and related difficulties.
  • Inlaying and chemical etching methods have normally been costly and process-time consuming.
  • a resinous polymer sheet material for use in preparing a product having surface decorative effects comprising a base layer or substrate; a printing composition layer forming a pattern or design on said base layer or substrate; a resinous polymer wear layer on said printing composition layer comprising substantially uniformly therein reactive polymerizable and cross-linkable monomeric materials; and a polymerization initiator capable of initiating a polymerization and cross-linking reaction to polymerize and to cross-link said reactive polymerizable and cross-linkable monomeric materials to. increase the melt viscosity of said resinous polymer wear layer.
  • the invention further provides a method of making a resinous polymer sheet material having surface decorative effects comprising laying down or forming a base layer or substrate; applying a printing composition layer forming a pattern or design on said base layer or substrate; applying to said printing composition layer a resinous polymer wear layer having substantially uniformly therein reactive polymerizable and cross-linkable monomeric materials; including in areas of said resinous polymer sheet material a polymerization initiator capable of initiating a polymerization and cross-linking reaction to polymerize and to cross-link said reactive polymerizable and cross-linkable monomeric materials; and heating the surface of said resinous polymer wear layer to cause said polymerization initiator to bring about a reaction polymerizing and cross-linking said reactive polymerizable and cross-linkable monomeric materials at the areas of said polymerization initiator, whereby the melt viscosity of said resinous polymer wear layer in said areas is increased.
  • the mechanically embossed flat, dead or dull mat finish or texture is not capable of resisting the softening and melting effects of the elevated temperatures during any subsequent fusion and/or blowing or foaming operations and therefore softens and melts sufficiently as to flow together and form a sleek, glossy or lustrous finish which contrasts sharply with the adjacent flat, dead or dull mat finish of the polymerized and/or cross-linked areas of higher melt viscosities.
  • a resinous polymer sheet material 10 comprising a base layer or substrate 11 of a relatively flat sheet backing material 12 and a potentially foamable polymer composition 13 which, after mechanical embossing at an elevated temperature and under pressure and after subsequent blowing and foaming at an even more elevated temperature, possesses a relatively high, blown or foamed, uninhibited cellular resinous polymer composition 14 and a relatively low, relatively unblown or unfoamed, inhibited, relatively or substantially non-cellular resinous polymer composition 16.
  • substantially non-cellular does not mean completely non-cellular but does indicate that the cells therein, if any, are very much smaller in size and very much fewer in number than the cells in the so-called cellular portions 14.
  • a printing ink composition 18, in the form of a desired pattern or design usually containing many different colors, is applied to the surface of the potentially foamable resinous polymer composition 13, prior to the mechanical embossing at the elevated temperature and pressure and the subsequent blowing and foaming at the even more elevated temperature.
  • the pattern or design of the printing ink composition 18 possesses certain predetermined areas or colors 20 which, in this embodiment, contain a blowing modifier, such as an inhibitor, and a free-radical polymerization initiator or catalyst, such as an organic peroxide.
  • a blowing modifier such as an inhibitor
  • a free-radical polymerization initiator or catalyst such as an organic peroxide.
  • other predetermined areas or colors 21 do not contain any blowing modifier or any free-radical polymerization initiator or any catalyst, for purposes to become clearer from a further reading an an understanding of this specification.
  • a resinous polymer composition in the form of a wear layer 22 is applied substantially uniform over the printing ink composition 18.
  • the blowing modifier or inhibitor restricts the blowing or foaming of the potentially foamable resinous polymer composition 13 in the areas A which correspond to and are in perfect registry with the areas 20.
  • blowing or foaming and expansion of the potentially foamable resinous polymer composition 13 is not restricted or deterred in the areas B which do not lie directly over the
  • the free-radical polymerization initiator or catalyst which is also present in areas 20 causes, for reasons which will be explained in greater detail hereinafter, the surface areas of the wear layer 22 lying directly over the areas 20 to have an embossed flat, dead or dull mat finish or texture, whereas the other areas B of the wear layer 22 not lying directly over the areas 20 and which do not contain any of the free-radical polymerization initiator or catalyst have a sleek, glossy or lustrous finish. The two types of finishes are in sharp contrast to each other.
  • the areas 20 not only contain the free-radical polymerization initiator or catalyst, but also contain the blow modifier or inhibitor, as well as a predetermined pigment or color of the printing ink composition 18, in accordance with the multicolor pattern or design.
  • the embossed, flat, dead or dull finish or texture in areas A are in complete and perfect registry with the relatively low, unblown or unfoamed portions 16 of the resinous polymer composition 13, as well as the predetermined pigment or color of the pattern or design.
  • the smooth, glossy or lustrous finish in areas B are in complete and perfect registry with the relatively high, blown or foamed portions 14 of the resinous polymer composition 13, as well as the other predetermined pigments or colors of the pattern or design.
  • the base layer or substrate 11 may comprise a relatively flat, fibrous backing sheet material 12 and/or a blown or unblown resinous polymer composition having a chemically embossed or unembossed surface and/or other relatively flat sheet materials.
  • a relatively flat, backing web or sheet material 12 may be used, if desired or required, as the base layer or substrate 11 for the resinous polymer sheet materials 10 of the present inventive concept.
  • a backing sheet material 12 may comprise a felted or matted fibrous sheet of overlapping, intermingled fibers and/or filaments; or a non-woven, knitted, woven or otherwise textile fabricated construction; or a sheet of resinous polymer composition; or paper or a paper product or similar or like equivalent constructions and materials.
  • a felted fibrous sheet material comprising inorganic fibers, such as asbestos; or organic fibers, such as cellulose, cotton, jute, or rayon; or synthetic or man-made fibers and/or filaments, such as polyolefins, polyamides, acrylics, glass, etc., is the most commonly employed backing sheet material but many others are equally suitable and are utilizable in special situations.
  • Such backing sheet materials are set forth in many prior art patents, such as United States Patents 3,293,094; 3,293,108 and 3,660,187.
  • Such a relatively flat backing sheet material 12 will depend to a large extent upon the particular product to be made and the particular subsequent use for which it is intended. Normally, such thicknesses are in the range of from 0,254 mm (10 mils) to 2,28 mm (90 mils), but other thicknesses, especially those greater than 2,28 mm (90 mils), may be used in special and particular circumstances.
  • the relatively flat backing sheet material 12 may be used by itself as tne base layer or substrate, or it may be used in conjuction with other sheet materials, such as, for example, a layer of potentially foamable or nonfoamable resinous polymer composition. Or the relatively flat, backing sheet material 12 may be omitted completely and the foamable or nonfoamable resinous polymer composition may be used by itself.
  • resinous polymer compositions may be made by well-known standard and conventional methods and may contain one or more synthetic resins, such as a polymer or copolymer of vinyl chloride, or other resins, such as plyurethanes, as the main constituent resin.
  • a blowing or foaming agent such as azonicarbonamide, if a blowing or foaming agent is desired; various accelerator/stabilizers or catalysts such as dibasic lead phthalate, zinc octoate, zinc oxide, lead octoate, dibasic lead phosphite, etc.; various light and/or heat stabilizers, and metallic soaps; plasticizers as dioctyl phthalate, butyl benzyl phthalate, dibutyl sebacate, etc.; coloring agents and pigments as titanium dioxide; solvents and diluents as methyl ethyl ketone, mineral spirits etc.; fillers as clay and limestone; and many other conventional and well-known additives and improvement agents.
  • a blowing or foaming agent such as azonicarbonamide, if a blowing or foaming agent is desired
  • various accelerator/stabilizers or catalysts such as dibasic lead phthalate, zinc octoate, zinc oxide, lead octo
  • blowing or foaming agent has a sufficiently high decomposition temperature that it is not activated or decomposed prematurely during the earlier procedures of heating, gelling, and the mechanical embossing to be described hereinafter.
  • blowing or foaming agents and their decomposition temperatures at which they release gas vigorously include: azodicarbonamide (199°C) (390°F.) N,N'-dimethyl-N,N'-dinitrosotere- phthalamide (104,4°C) (220°F.); azobisisobutyronitrile (î 14,6°C) (240°F.); p,p'-oxybis(benzene- sulfonylhydrazide (160°C) (320°F.) dinitrosopentamethylenetetramine (80%) (187,8°C) (370°F); p,p'- oxybis(benzenesulfonylsemicarbazide) (218,3°C) (425°F.); barium azodicarboxylate (248,9°C) (above 480°F) and many others.
  • decomposition temperature values relate to the release of gas vigorously in dioctyl phthalate.
  • the resinous polymer composition is also preferably a dispersion of a synthetic resin in a liquid medium.
  • the dispersion medium can be a plasticizer in the case of a plastisol, or water in the case of an aqueous latex, or it can be an organic solvent in the case of an organosol. Excellent results are obtained with a dispersion of a synthetic resin in a plasticizer as a plastisol and such form is the preferred and typical form for the application of the present invention.
  • a few preferred and typical plasticizers useful in forming such plastisols are dibutyl sebacate, diotcyl sebacate, dioctyl adipate, didecyladipate, dioctyl azelate, dibutyl phthalate, dicapryl phthalate, dioctyl phthalate, dibutoxy ethyl phthalate, tricresyl phosphate, octyl diphenyl phosphate, dipropylene glycol dibenzoate, butyl benzyl sebacate, dibenzyl sebacate, dibenzyl phthalate, butyl benzyl phthalate.
  • All the plastisol compositions set forth in the preceding table are foamable resinous polymer compositions, inasmuch as azodicarbonamide is included in all the formulations. Such a blowing agent would be excluded if a non-foamable resinous polymer composition was desired or required.
  • the plastisol may be doctored by a doctor blade, or roll coated, or poured, or cast, or otherwise applied to a strippable carrier which may be a steel belt, a rubber belt, release paper, or a felt or other fabric or material having a release coating thereon and subsequently stripped therefrom.
  • the plastisol may be doctored by a doctor blade, or roll coated, or poured, or cast, or otherwise applied and adhered to the carrying sheet material in a substantially uniform manner in a relatively uniform thin coating by procedures well-known in the art.
  • the thickness of such a plastisol coating as a foamable resinous polymer composition, as applied and still wet, is in the range of from 0,127 mm (5 mils) to 27 mm (50 mils), or even more, if so desired or required.
  • the plastisol After the plastisol has been applied to the carrying backing sheet material, it is then heated under relatively gentle or moderate heat in an oven or other suitable heating device for a period of time of from about 1 minute to about 4 minutes at an elevated temperature of from 115,6°C (240°F)., to 243,4°C (470°F)., but more normal commercially from 143,3°C (290°F)., to 176,7°C (35 0 " F )., whereby the plastisol firms and gels so that it can be more easily handled and processed subsequently.
  • the temperature and time relationships are mutually interdependent and the higher the temperature, the shorter is the required time, and vice versa.
  • the elevated temperature is not sufficiently high as to activate or to decompose the particular blowing or foaming agent which may be present as to cause blowing or foaming of the resinous polymer composition.
  • the gelled, firm resinous polymer composition is then cooled and is printed or coated with a suitable printing ink composition in the desired or required pattern or design which may possess many colors.
  • a suitable printing ink composition in the desired or required pattern or design which may possess many colors.
  • the particular pattern or design which is used does not relate to the essence of the invention and any suitable pattern or design may be selected.
  • predetermined parts or portions of the pattern or design printed on the surface of the resinous polymer composition contain a blow modifier or inhibitor in different amounts, concentrations, or types, and so forth, depending upon the variety of differential blowing or foaming effects desired.
  • a blow modifier or inhibitor in different amounts, concentrations, or types, and so forth, depending upon the variety of differential blowing or foaming effects desired.
  • a polymerization initiator or catalyst for a purpose to be described hereinafter more fully, with reference to certain reactive polymerizable monomers also to be described more fully hereinafter.
  • the concentration of the free-radical polymerization initiator or catalyst in the printing ink composition will vary and will range from about 1 percent by weight to about 35 or 40 percent by weight, and preferably from about 1 percent to about 10 percent by weight, based on the total weight of the printing ink composition.
  • free-radical polymerization initiators or catalysts as they are often referred to in the industry, are perhaps more properly identified as organic peroxides, or per-compounds, which materials are largely chemically characterized by the presence in their structure of the thermally unstable oxygen- oxygen grouping (that is, -0-0-, a peroxy group). Such a group decomposes, normally upon being heated to certain elevated temperatures, to form free radicals to initiate the polymerization reaction.
  • the specific free-radical polymerization initiator or catalyst which is selected for a particular polymerization or reaction depends upon the temperature at which the specific reaction or polymerization takes place, upon the rate of decomposition of the free-radical polymerization initiator or organic peroxide, upon the rate of generation or free radicals, upon the presence of metal ions or by the solvents of diluents in which the organic peroxides are often supplied commercially, upon the percent peroxide and the percent oxygen in the assay, upon the activation energy (k cal per mole), etc.
  • dicumyl peroxide is the preferred and typical organic peroxide or free-radical polymerization initiator or catalyst, of use with the majority of polymerizable reactive monomers. Such preference is due basically to the fact that dicumyl peroxide fits in very desirably with respect to its one minute half-life temperature in relationship to the normal gelling temperature of the plastisol used, to the normal fusion temperature of the resinous polymer composition used, and to the normal decomposition temperature of the blowing or foaming agent used (azodicarbonamide).
  • azodicarbonamide blowing or foaming agent used
  • di-butyl tin dilaurate would be a preferred and typical cross-linking catalyst, if a different resinous polymer composition, such as a polyurethane, is used.
  • resinous polymer composition such as a polyurethane
  • Other preferred and typical organic peroxides and per-compounds include:
  • compounds cover several classes of peroxides and encompass a very wide range, all of which, nevertheless, are utilizable under selected conditions, with particular reference to the plastisol gelling temperature, the plastisol and resinous polymer composition fusion temperatures, and the blowing and foaming temperatures, which, with respect to the preferred operating conditions of the present inventive concept, are normally commercially in the range of about 148,9°C (300°F)., 176,7°C (350°F)., and 201,7°C (395°F)., respectively.
  • a preferred range of peroxides is noted as possessing one minute half-lives of from 132,8°C (272°F). to 191,1°C (376°F)., with especially preferred commercial ranges of one minute half-lives from 157,7°C (305°F) to 173,9°C (345°F).
  • the concentration of the remaining constituents of the printing ink compositions which includes resins, pigments and dyes, solvents and diluents, blow modifiers and inhibitors, plasticizers, etc., are conventional and are within the ranges noted in the prior art, such as the previously mentioned United States Patents.
  • blow modifiers or inhibitors it is to be stated that, although essentially all of the blow modifiers or inhibitors mentioned in these United States Patents are utilizable within the broader aspects of the present invention, three preferred and typical examples of such are trimellitic anhydride, fumaric acid, and benzotriazole.
  • a few preferred and typical printing ink compositions are as follows:
  • a wear layer in the form of a resinous polymer composition or plastisol is then applied thereto.
  • a wear layer composition contains conventional or standard constituents, such as resins (preferred and typical being polyvinyl chloride, medium to low molecular weight), plasticizers, stabilizers, pigments or dyes (on rare occasion), solvent and diluents, viscosity improvement and controlling agents, and like additives and materials.
  • resins preferred and typical being polyvinyl chloride, medium to low molecular weight
  • plasticizers such as polyvinyl chloride, medium to low molecular weight
  • stabilizers such as polyvinyl chloride, medium to low molecular weight
  • pigments or dyes on rare occasion
  • solvent and diluents such as viscosity improvement and controlling agents, and like additives and materials.
  • concentrations of such constituents are conventional and standard and are in the ranges set forth in the previously cited United States Patents.
  • a further ingredient comprising one or more reactive polymerizable monomeric materials, the polymerization and/or cross-linking of which can be initiated by the previously described polymerization initiators or organic peroxides.
  • Such polymerization initiators are advantageously located in certain predetermined portions or colors of the pattern or design of the printing ink composition, whereby certain predetermined portions of the reactive polymerizable monomers lying directly thereover are polymerized and/or cross-linked, whereas certain other predetermined portions or colors of the pattern or design of the printing ink composition which do not contain any polymerization initiator therein do not polymerize and/or cross-link the reactive polymerizable monomers lying thereover.
  • the inherent viscosities of the polyvinyl chloride resins used in such wear layer compositions are in the range of from about 0.6 to about 1.2 but, depending upon conditions and circumstances, may be as high as about 1.6, as measured and determined by A.S.T.M. D-1 243-66 prior to the initiation of the mechanical embossing procedure, which will be more fully described hereinafter.
  • the reactive polymerizable monomers are included substantially uniformly in the wear layer and are polyfunctional and contain at least two olefinically unsaturated sites in its molecule.
  • Such monomers must be capable of polymerization at desired elevated temperatures usually higher than the plastisol gelling temperature but lower than the blowing agent decomposition temperature. Such polymerization takes place in all areas of the wear layer which are lying directly over the free-radical polymerization initiator or organic peroxide located in certain selected portions or colors of the printing ink composition.
  • Preferred and typical reactive polymerizable monomers include:
  • Such monomers are polyfunctional and include difunctional, trifunctional and tetrafunctional monomers. However, if desired, a certain amount of monofunctional monomers may be included in the wear layer in admixture with the polyfunctional monomers. Such combinations often possess unique and very desirable characteristics and properties.
  • monofunctional monomers When monofunctional monomers are included with the polyfunctional monomers, they are present in amounts of from about 5% by weight to about 50% by weight, based on the total weight of all monomers in the resinous wear layer formulation.
  • the total weight of all monomers in the wear layer is in the range of from about 5 parts by weight to about 40 parts by weight, based on 100 parts by weight of resin (phr) in the wear layer formulation, or preferably from about 15 parts by weight to about 35 parts by weight, based on 100 parts of resin (phr) in the resinous wear layer formulation.
  • the particular reactive polymerizable monomer or monomers which are selected for a particular use must, of course, be compatible with or dispersible in the resin representing the major constituent in the resinous wear layer formulation. It is usually contained in a copolymer, polymer or homopolymer of polyvinyl chlonde. That is, the reactive polymerizable monomer must be miscible or dispersible in substantially all proportions with the main resin and must be capable of being easily and intimately dissolved or dispersed therein without separating into separate, distinct layers or portions, or occupying separate, discrete portions or phases in the resinous wear layer composition. And, of course, the reactive polymerizable monomer must also be relatively inert at low temperatures and non-reactive with respect to the other constituents of the resinous wear layer composition.
  • the thickness of such a resinous wear layer composition is in the range of from 0,051 mm (2 mils) to 0,762 mm (30 mils), or greater, if so required by special circumstances, requirements, or conditions.
  • the wear layer containing the reactive polymerizable monomers After the wear layer containing the reactive polymerizable monomers has been applied and adhered to the printed pattern or design of the printing ink composition, it is heated under moderately gentle heat in an oven or other suitable heating device for a period of time of from about 1 minute to about four minutes at an elevated temperature of from 11 5,6°C (240°F) to 243,3°C (470°F), whereby it hardens or firms and gels so that it can be easily handled in further operations.
  • the temperature and time are so interrelated as to be interdependent and the higher the temperature, the shorter is the time of application of the heat, and vice versa.
  • the elevated temperature however, must not be that high as to activate or decompose the blowing or foaming agent which is normally present. Also, the temperature and the time must not be that great as to bring about a polymerization of the reactive polymerizable monomers in the wear layer. " .
  • the polymerization and cross-linking of the monomers in the wear layer take place during the embossing procedure which follows and which takes place under about the same temperature as the preceding gelling procedure but under additional pressure whereby the embossing of the surface of the wear layer and the polymerization of the reactive polymerizable monomers take place in the same operation.
  • such temperature are, of course, below the temperature at which the blowing or foaming agent in the plastisol composition will be activated or decompose to release their gases in a vigorous manner.
  • the depth of the mechanical embossing may be as little as a fraction of 0,0254 mm (a mil) or it may be as much as about 0,381 mm (15 mils), but preferably is from 0,0254 mm (1 mil) to 0,102 mm (4 mils), depending upon the type, thickness, and the nature of the wear layer being so embossed mechanically, upon the decorative effect which is desired or required, upon the type and the form of the mechanical embossing, and so forth.
  • the entire surface of the wear layer is embossed so as to give it temporarily the desired flat, dead or dull mat finish or texture allover.
  • a finish or texture is substantially completely lacking in brilliance, gloss, luster or sheen.
  • the surface may be roughened, corrugated, coarse, lined or knurled in a regular or irregular, predetermined or random fashion and may possess numerous very small knobs, projections, ridges, points, or protuberances to give it the desired flat, dead or dull mat appearance.
  • the mechanical embossing may also take the form of very many, very fine lines which are straight and parallel are swirling curves, as many as about 60 or 80 or even 100 or more lines per 25,4 mm (inch), or it may be the result of pressing paper, textured materials or fabrics, woven, knitted or nonwoven against the surface of the wear layer to create thereon the desired finish or texture.
  • the mechanical embossing to yield the desired flat, dead or dull mat finish or texture or other finishes may take place under pressures which may be as low as 0,0137 MPa (2 pounds per square inch gauge) up to 2,055 MPa (300 pounds per square inch gauge), depending upon the existing temperature which is in the range of from 11 5,6°C (240°F), to 243,3°C (470°F). If the pressure is applied in a press platen, the pressure may be maintained for a period of time of from about 10 seconds to as much as about 4 minutes. If the pressure is applied by means of a heated embossing roll, then the temperatures and the pressures will be in the higher portions of the aforementioned ranges, whereas the time of the application of the pressure will be correspondingly relatively short.
  • the passing of or the wrapping of the resinous polymer sheet material around a portion of the periphery of the heated embossing roil can be used to extend the duration of the application of heat.
  • the pressures which are exerted, however, must be sufficient as to establish a good intimate contact between the heated embossing surface and the resinous polymeric materials being embossed.
  • the temperatures and the pressures which are realized during the embossing procedure are normally sufficient to activate or decompose the free-radical polymerization catalyst or organic peroxide in the predetermined portions of the printing ink composition which will bring about a polymerization or a cross-linking of the reactive polymerizable monomers lying over such predetermined portions.
  • such portions of the wear layer possess an increased melt viscosity therein and a harder, more resistant surface which is capable of resisting any softening or melting tendencies during the subsequent heating involved in the blowing or foaming procedure. In this way, such portions are capable of retaining their flat, dead or dull mat embossed surface finishes or textures through the higher heating during the blowing and foaming operations.
  • those predetermined portions of the wear layer which lie over those portions of the printing ink composition which do not contain any free-radical polymerization initiator or organic peroxide are not materially polymerized or cross-linked, do not possess an increased melt viscosity and do not obtain a harder or more resistant surface and, consequently, when they are exposed to the greater heat of the blowing or foaming operation, they will not be able to resist any softening or melting tendencies, which are created and they will melt and soften and flow to fuse into a glossy, lustrous finish having a relatively high brilliance and sheen.
  • Such a glossy, lustrous surface is very smooth and very planar and very reflective of any light incident thereon, as contrasted sharply to the flat, dead or dull mat finish which is not smooth or sleek and is not as reflective of any light incident thereon.
  • the contrast created by these two types of finishes or textures is striking.
  • the final resulting product in one form thereof, greatly resembles a ceramic tile flooring such as is commonly found in bathrooms, both as floor and as wall surfaces.
  • the sleek, glossy or lustrous finish greatly resembles the surface of a glazed or fired ceramic tile, whereas the flat, dead or dull mat surface greatly resembles the grout or cementitious materials which are placed between the glazed ceramic tile...
  • the multi-layered assembly comprising: the backing sheet material and/or the potentially foamable (or non-foamable) plastisol; the printed pattern or design of the printing ink composition, portions or colors of which contain modifiers or inhibitors and free-radical polymerization initiators or organic peroxides, other portions or colors of which do not contain modifiers or inhibitors or free-radical polymerization initiators or organic peroxides; and the upper wear layer containing substantially uniformly therein the reactive polymerizable monomers, after being mechanically embossed over its entire surface, is heated to a sufficiently elevated temperature which is capable of fusing the resins in the resinous polymer compositions and which is also capable of activating or decomposing the blowing or foaming agents in the potentially foamable plastisols to cause vigorous blowing or foaming therein.
  • the surface of the wear layer is raised to the more highly elevated temperature whereby those areas thereof, which do not possess the higher melt viscosities or the polymerized or cross-linked monomers, soften, melt and flow to form the sleek, glossy and lustrous surfaces. And, naturally those other areas which possess the higher melt viscosities and the polymerized or cross-linked monomers resist the higher temperatures and do not soften, melt or flow but retain their flat, dead or dull mat surface finish or texture.
  • the temperature of the entire assembly must reach the fusion temperature of the resins in order to obtain the desired maximum strength.. Fusion is normally obtained at a temperature of from 162,8°C (325°F) to 243°C (470°F), depending upon the particular polymeric product being used.
  • blowing and foaming temperatures are ambient air temperatures and not temperatures of the product exposed to such ambient air temperature.
  • the plastisol or the originally potentially foamable resinous polymer composition initially contained a blowing or a foaming agent therein, such as azodicarbonamide, which was substantially uniformly distributed therein.
  • a blowing or foaming agent such as azodicarbonamide
  • those portions of the printing ink composition 18 lying in zones A additionally contained a blowing or foaming modifier, such as an inhibitor, and hence those portions of the resinous polymer composition lying thereunder in zones A are relatively unblown or unfoamed due to the inhibiting action of the blowing or foaming inhibitor.
  • those portions of the printing ink composition 18 lying in zones B did not contain any blowing or foaming modifier, such as an inhibitor, and hence such portions of the resinous polymer composition lying thereunder in zones B are relatively blown or foamed substantially completely.
  • blowing or foaming modifier such as an inhibitor
  • those portions of the printing ink composition 18 in zones A also contained a free-radical polymerization initiator or organic peroxide which was activated or decomposed during the embossing operation operation to polymerize and/or cross-link the reactive polymerizable monomer in the wear layer 22 and to increase the melt viscosities of such portions. As a result, such portions retained their flat, dead or dull mat finish or texture throughout the blowing or foaming operation.
  • those portions of the printing ink composition 18 in zones B did not contain any free-radical polymerization initiator or organic peroxide and there was no polymerization or cross-linking of the polymerizable monomer in the wear layer thereover and the melt viscosities of such portions did not increase. As a result, such portions were not able to resist the elevated temperatures of the blowing and foaming cycle, and they melted, softened and flowed to form sleek, glossy and lustrous surfaces in such zones B.
  • the sleek, glossy or lustrous finish areas should have gloss levels in the range of from about 15 to about 90, or even higher; the flat, dead or dull mat finish areas should have gloss levels in the range of from about 70 down to about 3, or even less; with the differences in the gloss levels between the two contrasting finishes being in the range of at least about 10 in gloss level ranges below 50 and at least about 20 in gloss level ranges equal to or above 50.
  • Such numerical gloss level values are determined by the procedures set forth in A.S.T.M. 523-67 (1972) at an angle of 60°.
  • the principles of the present inventive concept are equally applicable to the obtaining of a sleek, glossy or lustrous finish in some certain selected areas and the obtaining of even more sleek, glossy or lustrous finishes in certain other selected areas, again keeping the differences in the gloss level values greater than about 20, inasmuch as the gloss levels involved in such embodiment will be greater than about 50.
  • Such sleek and very sleek contrasts may be obtained by omitting the mechanical embossing procedure with a roughened surface and by substituting therefor a platen-pressing or press-rolling operation with a very smooth, highly polished surface, whereby the entire surface of the resinous wear layer is given an extremely smooth, sleek, shiny, glossy or lustrous finish.
  • High temperature and pressures are subsequently similarly employed, as previously described in connection with the blowing and foaming step, whereby the polyfunctional reactive polymerizable and cross-linkable monomers in the wear layer lying over the polymerization and cross-linking initiators in the printing ink composition, having been cross-linked during the heated platen-pressing or press-rolling operation, effectively resist such heating and pressure and "freeze" those particular areas, whereby they are capable of retaining their extremely sleek, shiny, glossy or lustrous finish throughout such subsequent blowing or foaming operation.
  • those other areas which contain the monomeric materials not lying over any polymerization or cross-linking initiators or organic peroxides still contain such monomeric materials in unpolymerized and un-cross-linked state and hence, soften, melt and flow and thus lose some of their extremely sleek, shiny, glossy or lustrous finish but do develop or retain sufficient of their previous extremely sleek, shiny, glossy or lustrous finish at least about 20 units in gloss level, less than the gloss level of the extremely sleek, shiny, glossy or lustrous finish.
  • the blowing or foaming action of the potentially foamable plastinol is of such a strong and vigorous nature that the gases which are developed or liberated by the blowing or foaming agent tend to escape upwardly from the heated plastinol and tend to enter the wear layer to undesirably affect the smoothness and evenness of the wear layer surface and particularly those areas thereof having a low melt viscosity, or substantially no polymerized and/or cross-linked monomers therein, or sleek, glossy or lustrous surfaces. Such could be ruinous to the smoothness of such surfaces and would be undesirable from an aesthetic viewpoint. Additionally, such affects the strong contrast between the sleek, glossy or lustrous surfaces and the embossed, flat, dead or dull surfaces adjacent thereto.
  • This undesirable effect can be avoided by placing a relatively thin barrier coat or layer having a thinness of only about 0,152 mm (6 mils) or less, down to about 0,0854 or 0,0508 mm (1 or 2 mils), on top of the potentially foamable plastisol before the printed pattern or design is applied thereto, or alternatively such a barrier coat is applied over the printed pattern or design before the application of the wear layer.
  • a barrier coat or film effectively prevents the gases from escaping upwardly from the blowing or foaming plastisol and entering the wear layer.
  • the barrier layer is applicable as a film but is normally applied as a plastisol resinous polymer composition in a thin layer of a resin such as a vinyl chloride polymer or copolymer having a relativley very high molecular weight. Gelling of such a plastisol barrier layer naturally follows at an elevated temperature below the activation, or decomposing temperature of the blowing or foaming agent and the polymerization initiator or organic peroxide.
  • the thickness of the barrier coat or layer must not be that great as to prevent the blow modifier or inhibitor from exerting its blow modifying or inhibiting effects downwardly through the barrier layer into the plastisol during the blowing operation or the polymerization initiator from exerting its effects upwardly during the polymerization and/or cross-linking of the reactive polymerizable monomers.
  • additives and agents such as, for example, ethoxylated nonylphenol, a viscosity depressant, or other plasticizers and stabilizers solvents or diluents, fillers, etc., can be used.
  • the base layer or substrate 11 may comprise simply a fibrous backing sheet material and that other layers, such as non-foamable or potentially foamable resinous polymer compositions or plastisols or other sheet materials may be omitted.
  • FIGS 4 and 4A depict, respectively, the resinous polymer sheet material before and after the completion of the embossing and subsequent heating steps in its manufacture.
  • a resinous polymer sheet material 30 comprising a relatively flat backing sheet material 32 of fibrous nature, such as an asbestos felt upon which is printed a printing ink composition 38 in the form of a desired pattern or design in a plurality of colors, as usual.
  • a smoothing of leveling resinous polymer coating such as an acrylic coating, may be applied to the asbestos felt 32, if its surface is too uneven, hairy, fibrous, or irregular before the printing of the printing ink composition 38 thereon.
  • a wear layer 42 is then applied to the surface of the printed pattern or design in the usual way and contains therein polymerizable reactive monomers substantially uniformly.
  • the wear layer 42 is then embossed in overall fashion under sufficient pressure and at a sufficiently elevated temperature for a sufficiently long period of time as to create on its surface the desired finish or texture, such as a flat, dead or dull mat finish or texture.
  • the reactive polymerizable monomers in the wear layer 42 are polymerized and/or cross-linked and the melt viscosity is increased but only in those portions thereof which lie directly over the free-radical polymerization initiator or organic peroxide in the printing ink composition. All other areas which do not lie over any free-radical polymerization initiator or organic peroxide do not have any polymerized and/or cross-linked monomers in the wear layer and the melt viscosity of such areas is also substantially unchanged.
  • the mechanically embossed sheet material is raised to an even more elevated temperature, somewhat similar to the temperature which would exist under blowing of foaming conditions, the polymerized and/or cross-linked portions of the wear layer which also have a relatively higher melt viscosities, are able to resist the softening and the melting effects of such heating and retain their mechanical embossment and remain flat, dead or dull mat in appearance.
  • the relatively flat, dead or dull mat finish or texture is designated in Figure 4A by the reference letter A and it is to be noted that such areas are in complete and precise registry with the areas 40 containing the free-radical polymerization initiator or organic peroxide and with the particular color of the printed pattern or design containing such material.
  • the relatively sleek, glossy or lustrous surfaces are designated by the reference letter B and are over areas of the printing ink composition which do not contain any free-radical polymerization initiator or organic peroxide and thus in complete and precise registry with such areas which protruberances are noted in the surface of the wear layer 42 in the zones A.
  • the base layer or the substrate 11 may comprise simply a resinous polymer composition and that other layers, such as a relatively flat, fibrous sheet material, or other sheet materials may be omitted.
  • a resinous polymer sheet material 50 comprising a relatively flat and relatively thin sheet of release paper 55 of a conventional character as are commercially available.
  • release paper 55 is deposited or laid down a layer of a potentially foamable resinous polymer composition 53 which contains a conventional blowing or foaming agent such as azodicarbonamide.
  • the surface of the potentially foamable plastisol 53 is gelled and is then printed with a printing ink composition 58 which contains a free-radical polymerization initiator or organic peroxide and a particular pigment-or color in areas 60, whereas other areas 61 do not contain any free-radical polymerization initiator or organic peroxide but do contain pigment or coloring agent. No blow modifiers or inhibitors are included in any portion of the printing ink composition 58.
  • a wear layer 62 is then applied to the surface of the printing ink composition 58 and contains substantially uniformly therein quantities of a reactive polymerizable monomer.
  • the wear layer is then embossed mechanically under sufficient pressure and at a sufficiently elevated temperature and for a sufficiently long period of time as to create thereon the desired flat, dead or dull mat finish or texture in an overall pattern of embossment, during which time the reactive polymerizable monomer is normally polymerized and cross-linked.
  • a conventional blowing or foaming operation then follows at an even more elevated temperature whereby the blowing or foaming agent causes the expansion of the resinous polymer composition.
  • Such expansion is well shown in Figure 5A.
  • the higly polymerized or cross-linked monomers in the areas 60 which areas also possess higher melt viscosities, resist the softening or melting effects of the heat during the blowing and foaming operation and such areas 60 remain in a. desired flat, dead or dull mat finish or texture.
  • the areas 61 which do not lie over any portions of the printing ink composition 58 which contain any free-radical polymerization initiator or organic peroxide are not polymerized or cross-linked and do not have higher melt viscosities and are unable to resist the softening or melting tendencies created during the heating of the blowing and foaming cycle and hence such areas melt and flow together to form a sleek, glossy or lustrous surface which contrasts sharply with the kann, dead or dull mat finish or texture of the areas 60. Areas A are again flat, dead or dull, whereas areas B are sleek, glossy or lustrous.
  • the blowing or foaming is uniform and no chemically embossed effects are realized on the surface of the wear layer. Small protuberances are noted in the surface of the wear layer 62 in zones A. These will be discussed in greater detail hereinafter.
  • the relatively flat and relatively thin sheet of release paper is removed from the bottom surface of the resinous polymer composition subsequent to the blowing of foaming cycle. However, if the resinous polymer composition, printing ink composition, and wear layer possess sufficient strength as to permit the handling thereof, or if another carrier is supplied therefor, then the release paper may be removed prior to the blowing and foaming operation.
  • the resinous wear layer 62 may have incorporated substantially uniformly therein a polymerization initiator or organic peroxide which is activatable or decomposable at an even higher temperature than the decomposition or activation temperature of the polymerization initiator or organic peroxide in the printing ink composition 58.
  • Zones A which contain polymerized and/or cross-linked monomers have higher melt viscosities retain their appearance and their protuberances. Zones B develop their sleek, glossy or lustrous appearance, as before. Thus far, only the polymerization initiator in zones A have been activated and/or decomposed. The polymerization initiator or organic peroxide in the wear layer has not been activated or decomposed as yet because it possesses a higher activation temperature.
  • the polymerization initiator or organic peroxide in the wear layer is activated or decomposed, whereby all the reactive polymerizable monomer in the wear layer, including the zones B, are polymerized and/or cross-linked.
  • the surface of the wear layer 62 in zones A has an embossed, flat, dead or dull textured finish
  • the surface of the wear layer 62 in zones B has a sleek, glossy or lustrous finish but both zones A and B contain high concentrations of polymerized and or cross-linked reactive polymerizable monomers and both portions have relatively high melt viscosities.
  • FIGS 6 and 6A there is illustrated still another modification of the principles of the present inventive concept.
  • a conventional base layer or substrate comprising a relatively flat, fibrous backing sheet material 72 such as an asbestos felt, upon which is applied a printing ink composition 78 in the form of a desired multi-colored pattern or design wherein certain predetermined portions or colors 80 contains a free-radical polymerization initiator or organic peroxide and a particular pigment or coloring agent.
  • Other predetermined printed portions 81 of the printing ink composition 78 on the surface of the fibrous backing sheet material 72 contain no free-radical polymerization initiator or organic peroxide but do contain a different pigment or coloring agent.
  • there is no potentially foamable plastisol involved there is no need for a blowing or foaming modifier or inhibitor in the printing ink composition 78 or in any portion thereof.
  • An upper wear layer 82 comprising a resinous polymer composition is then applied to the surface of the printing ink composition 78 and contains substantially uniformly therein a reactive polymerizable monomeric material.
  • the wear layer 82 is then heated to a relatively low temperature in order to gel and harden or form its surface and to facilitate its subsequent handling and processing. No mechanical embossing of any type takes place on the surface of the wear layer 82, and in this respect it differs from the modification previously discussed with reference to Figures 4 and 4A.
  • a resinous polymer sheet material 90 comprising a conventional, relatively flat, fibrous sheet material 92 such as an asbestos felt.
  • a resinous polymer composition 94 which is shown in the blown condition due to the prior inclusion therein of a conventional blowing or foaming agent, such as azodicarbonamide, which was activated and decomposed by exposure to heat at a sufficiently elevated temperature for a sufficient period of time.
  • a barrier coat or layer 95 is situated atop the blown cellular resinous polymer composition 94 and serves to prevent any of the gases developed and liberated during the blowing and foaming operation from escaping.
  • a printing ink composition 98 is applied to the surface of the barrier coat 95 in the form of a multi-colored pattern or design. Portions of the printed pattern or design contained in a free-radical polymerization initiator or organic peroxide in areas 93, whereas certain other areas did not contain any free-radical polymerization initiator or organic peroxide.
  • zones A Such differences in appearance, of course, is caused by the fact that the free-radical polymerization initiator or organic peroxide in zones A caused a polymerization and/or cross-linking of the reactive polymerizable monomeric material in the wear layer 91, along with an increase in the melt viscosity thereat, whereby the mechanical embossment in such zones survived the heating at the elevated temperatures of the blowing and foaming cycle.
  • zones B whereat there was no free-radical polymerization initiator or organic peroxide in the printing ink composition 98, there was correspondingly no polymerization and/or cross-linking of the reactive polymerizable monomeric materials in the wear layer 91, and there was no increase in the melt viscosity in such zones B.
  • Such areas B are no longer embossed mechanically and they are no longer flat, dead or dull mat finished or textured but have become sleek, glossy and lustrous in appearance.
  • FIG 8 there is illustrated another modification of the basic principles of the present inventive concept.
  • a resinous polymer sheet material 100 comprising a conventional, relatively flat, fibrous sheet material, such as an asbestos felt.
  • Applied to the fibrous backing sheet material 102 is a layer of a resinous polymer composition 104 which is shown in an unblown or unfoamed state inasmuch as there was no blowing of foaming agent originally included in the plastisol composition. In the absence of blowing or foaming, the resinous polymer composition is non-cellular in the final product.
  • a printing ink composition 108 is applied to the surface of the resinous polymer composition 104 in the form of a multi-colored pattern or design. Portions of the printing ink composition 108 contains a free-radical polymerization initiator or organic peroxide, such as in areas 103, whereas other portions of the printing ink composition 108 do not contain any free-radical polymerization initiator or organic peroxide, as in areas 106.
  • the final height of the resinous polymer sheet material 100 is considerably less than that of Figure 7 which, as noted previously, did contain a blowing or foaming agent, such as azodicarbonamide, in its resinous polymer composition 94.
  • a blowing or foaming agent such as azodicarbonamide
  • Such difference in appearance is caused by the fact that the free-radical polymerization initiator or organic peroxide in zones A caused a polymerization and/or cross-linking of the reactive polymerizable monomeric material in the wear layer 101, along with an increase in the melt viscosity thereat, whereby the mechanical embossment in such zones A survived the heating at the elevated temperatures of the fusion cycle.
  • zones B whereat there was no free-radical polymerization initiator or organic peroxide in the printing ink composition 108 there was correspondingly no polymerization and/or cross-linking of the reactive polymerizable monomeric materials in the wear layer 101, and there was no increase in the melt viscosity in such zones B.
  • Such areas 106 were not able to resist the softening, melting and flowing tendencies created by the elevated temperatures during the fusion of the resins.
  • Such areas B are no longer mechanically embossed and they are no longer flat, dead or dull mat finished but have become sleek, glossy and lustrous.
  • Preferred and typical printing ink compositions for such a modification are as follows:
  • the structure of the product of this embodiment would be identical to the structure of the product illustrated in Figures 2 and 3, except for the reversal of the sleek, glossy or lustrous finish areas and the flat, dead or dull texture areas.
  • the portions of the wear layer lying over the polymerization initiator are relatively highly polymerized and cross-linked and have relatively high melt viscosities, whereas the portions of the wear layer lying over the blowing modifier or inhibitor are relatively low in polymerized or cross-linked monomer and have relatively low melt viscosities.
  • the polymerization initiator or organic peroxide may be contained in several different portions or colors of the printed pattern or design in several different concentrations. With the proper selection of desired varying concentrations several varying gradations of surface finishes or textures may be obtained. Sharpness of individual contrast may be lessened to some degree but a much greater variety of effects, finishes and textures is thus available.
  • Such variations and gradations of surface finishes and textures is also obtainable by the use of several different polymerization initiators or organic peroxides having several different levels or degrees of activity or several different temperatures of activation or decomposition.
  • Polymerization initiators or organic peroxides which have greater activity tend to polymerize the reactive polymerizable monomers to a greater degree and to increase the melt viscosity of the corresponding portions of the wear layer to a greater extent, whereby greater resistance is created to the melting, softening and flowing effects during the blowing and foaming cycles.
  • the placing of a high activity polymerization initiator or organic peroxide in one area of the printed pattern or design will tend to maintain the embossed flat dead or dull mat finish applied during the embossing procedure, whereas the placing of a low activity polymerization initiator or organic peroxide in a different area of the printed pattern or design will tend to permit the embossed flat dead or dull finish or texture to partially disappear to yield a different texture and/or gloss level or degree for the sleek, glossy or lustrous finish.
  • multiple mat and gloss and multiple finish and texture levels are obtainable.
  • an additional effect is obtainable by including an additional polymerization initiator or organic peroxide having a relatively high temperature of activation or decomposition in the wear layer in a substantially uniform manner.
  • the several different polymerization initiators or organic peroxides may be activated or decomposed at several different stages of the procedure whereby several different finishes or textures may be obtained. Then, at a much later stage, such as, for example, during the blowing and foaming cycle, the high temperature polymerization initiator or organic peroxide may then be activated to polymerize and/or cross-link the reactive polymerizable monomers in the entire resinous wear layer. Such would tend to increase the melt viscosities of all the different areas of the resinous wear layer as an overall effect.
  • a resinous wear layer such as described previously herein, is cast upon or otherwise formed on a suitably textured or embossed surface, such as a coarsely textured, parchment-type release paper, or other roughened, uneven, crinkled, rugose, or bumpy surface, or any similar or like protuberant or irregular surface having release properties and characteristics given to it.
  • the resinous wear layer composition is sufficiently fluid as to flow into and completely fill all the nooks and crannies, recesses and niches of the textured or embossed surface and thus to assume surface features and characteristics substantially identical thereto.
  • a surface being so irregular, uneven, pebbly or grainy that it does not reflect light regularly but more or less scatters it, would present a flat, dead or dull mat textured or embossed appearance to the eye, if the release surface were to be removed therefrom so that one could see the shaped surface of the resinous wear layer composition.
  • a printing ink composition or a plurality of such compositions, such as described previously herein, is applied or otherwise deposited on the surface of the cast resinous wear layer composition, after it has been gelled by conventional and standard procedures.
  • a desired design or pattern is thus applied, and, as described previously herein, certain predetermined areas of the printed pattern or design contain polymerization initiator or organic peroxide and, if desired, also a blowing of foaming modifier or inhibitor, whereas other predetermined areas of the printed pattern or design contain either (1) no polymerization initiator or organic peroxide at all, or (2) a different concentration of the same polymerization initiator or organic peroxide, or (3) a different polymerization initiator or organic peroxide having a different level or degree of activity or a different temperature of activation or decomposition.
  • the printing ink composition is then dried.
  • a resinous barrier coat such as described orevinusty herein, may then be applied to or otherwise deposited on the dried printed pattern or design of the printing ink composition.
  • a base layer or substrate preferably comprising a relatively flat, fibrous backing sheet of asbestos fibers, such as described previously herein, and a potentially foamable resinous polymer composition, such as a polyvinyl chloride plastisol, also as described previously herein is then laminated or otherwise adhered to the surface of the barrier coat, preferably under pressure and at elevated temperatures in a laminator, to form a unitary, integral structure.
  • a potentially foamable resinous polymer composition such as a polyvinyl chloride plastisol
  • the strippable coarsely textured release surface upon which the resinous wear layer was originally cast or formed is then removed and reveals a suitable textured or embossed surface on the resinous wear layer, precisely corresponding to the textured or embossed surface or the release material.
  • Heating to an even more elevated temperature in a fusion or blowing or foaming oven atmosphere brings about several actions.
  • those portions of the resinous wear layer which do not contain any polymerized and/or cross-linked reactive polymerizable monomers and which do not possess relatively high melt viscosities soften and melt at such temperatures and flow to form a sleek, glossy or lustrous surface or finish, whereas those other portions of the resinous wear layer which do contain polymerized and/or cross-linked reactive polymerizable monomers and which possess relatively higher melt viscosities are able to resist the softening and melting tendencies at such elevated temperatures and do not flow but maintain their original textured or embossed flat, dead or dull surfaces.
  • blowing or foaming agent such as azodicarbonamide
  • a blowing or foaming agent such as azodicarbonamide
  • the final product is, of course, substantially similar to the final product obtained in the previously described methods but possesses the procedural advantage that no separate mechanical embossing step is required.
  • the resinous barrier coat is applied to the dried printed pattern or design of the printing ink composition, prior to the heating of the printing ink composition and the polymerization initiator therein and the resinous wear layer and the reactive polymerizable monomer therein to bring about the polymerization and/or cross-linking of the reactive polymerizable monomer.
  • the resinous barrier coat may be omitted completely or, if desired, it may be applied or otherwise adhered to the resinous wear layer prior to the application of the printed pattern or design.
  • the important function to be realized is that the polymerization initiator in the printing ink composition be able to bring about the polymerization and/or cross-linking of the reactive polymerizable monomer and that the barrier coat is present, if needed, when the potentially foamable resinous polymer composition is subsequently blown or foamed and the. generated gases are released.
  • FIG 9 there is illustrated a resinous polymer sheet material 110 comprising a typical, relatively flat, backing web or sheet material 112 similar to the backing sheet material 12 described previously.
  • Such resinous polymer composition 113 is then processed as described previously herein, including, for example, a heating, gelling and firming, and cooling operation, and is printed or coated with a suitable printing ink oomposition 118 having a desired pattern or design of various colors, such as 118a, 118b, 118c, 118d, and 118e.
  • a relatively thin barrier coat or layer 115 such as the previously described barrier coat or layer, may be placed over the potentially foamable resinous polymer compositions 113, either before the printed pattern or design 118 is applied thereto, or, as shown in Figure 9, after the printed pattern or design is appl ed to the resinous polymer composition 113.
  • the purpose of such a barrier coat or layer has been described previously herein.
  • Heating and fusion, as well as blowing or foaming takes place as described previously.
  • the mechanical embossing of the surface of the wear layer 122 is retained substantially uniformly throughout, even after such operations.
  • Figure 10 shows a relatively flat, resinous polymer sheet material 120 comprising: a fibrous backing layer 112, a printing ink composition 118 uniformly containing a polymerization initiator, catalyst, or organic peroxide; a barrier coat or layer 115; and a wear layer 122, all substantially as described previously with particular reference to Figure 9.
  • a resinous polymer composition 123 is employed which contains a blowing or foaming agent. The previously described procedures of heating, gelling and firming of the resinous polymer composition 123 and of the wear layer 122, along with the subsequent overall mechanical embossing of the surface of the gelled wear layer 122, and the other previously described procedures take place, followed by conventional heating and fusion, and blowing or foaming in a fusion oven.
  • Figure 10 illustrates the blown resinous polymer sheet material 123, subsequent to the heating, fusion and blowing or foaming operations. The mechanical embossing on the surface of the wear layer 122 is retained substantially uniformly throuqhout.
  • Figure 11 shows a relatively flat, resinous polymer sheet material 130 comprising: a fibrous backing layer 112; a resinous polymer composition 133 containing a blowing or foaming agent; a printing ink composition 138 substantially uniformly containing equal concentrations and amounts of a free radical polymerization initiator, catalyst, or organic peroxide in all portions of areas thereof, as well as a blowing or foaming modifier or inhibitor which is contained only in certain selected portions or areas thereof 138a of the printing ink composition layer 138; a relatively thin barrier coat or layer 115; and a resinous polymer wear layer 122 which contains a reactive polymerizable monomeric material substantially uniformly therein.
  • a blowing or foaming agent has been uniformly included in the resinous polymer composition 133 and it is heated and fused and blown or foamed, as illustrated. However, due to the presence of the blowing or foaming modifier or inhibitor which is present in certain selected portions or areas 138a of the printing ink composition 138, the blowing or foaming operation proceeds selectively as is well known in the chemical embossing art, and the finished embossed product is illustrated in Figure 11.
  • a resinous polymer sheet material 140 comprising: a typical, relatively flat, backing web or sheet material 122; a resinous polymer composition 143 which is potentially foamable or non-foamable, as desired or required; a substantially uniform resinous polymer coating such as a clear printing ink composition 144 which contains substantially uniformly therein from about 1% to about 35% or 40% by weight, and preferably from about 1% to about 10% by weight, of a polymerization initiator, catalyst, or organic peroxide; a printing ink composition 148 which does not contain any polymerization initiator, catalyst, or organic peroxide; a relatively thin barrier coat or layer 145, if a blowing or foaming agent is included in the resinous polymer composition layer 143; and a wear layer 142 containing substantially uniformly therein one or more reactive polymerizable monomeric materials.
  • a clear printing ink composition 144 which contains substantially uniformly therein from about 1% to about 35% or 40% by weight, and preferably from about 1% to about 10% by weight
  • Figure 12 illustrates the resinous polymer sheet material 140, either immediately prior to the heating and fusion, and blowing or foaming operation (if a blowing of foaming agent is present), or subsequent to the heating and fusion operations, if no blowing or foaming agent was present.
  • the mechanical embossing on the entire surface of the wear layer 142 is retained substantially uniformly throughout these operations of heating, fusion, blowing or foaming.
  • Still another embodiment of the present invention leading to the retention of the overall mechanical embossing on the surface of the wear layer through the heating and fusion, and blowing or foaming operations is describable without the need or the necessity for still another Figure in the drawings.
  • Such embodiment excludes the presence of any polymerizable initiator, catalyst, or organic peroxide from the printing ink composition, as in Figures 9-11, and also excludes the presence of any polymerization initiator, catalyst, or organic peroxide existing in a separate layer, as in Figure 12.
  • the polymerization initiator, catalyst, or organic peroxide is included directly and uniformly in the wear layer containing the reactive polymerizable monomeric materials, usually from about 0.5% by weight to about 5% by weight and preferably about 1 % to about 2% by weight based on the weight of the reactive polymerizable monomeric materials.
  • the polymerizable initiator, catalyst, or organic peroxide may be included in the barrier coat 115 of Figure 9 from about 0.08% to about 0.8% by weight and preferably from about 0.16% to about 0.32% by weight based on the total weight of the barrier coat composition.
  • a resinous polymer sheet material such as illustrated in Figures 1-3 of the drawings is made by the following procedures:
  • Zones B are printed with a standard or conventional printing ink composition containing a predetermined pigment but which does not contain any blow modifier or inhibitor or any free-radical polymerization initiator or organic peroxide.
  • standard or conventional printing ink composition comprises:
  • Zones A are printed with the following printing ink composition containing a different pigment or coloring agent: Parts
  • the printed, gelled potentially foamable plastisol is then allowed to dry and a wear layer is applied thereto to a wet thickness of about 0,038 cm (0.015 inch) and having the following formulation:
  • Gelling and firming of the wear layer plastisol is accomplished by heating in an oven atmosphere having an elevated temperature of just under 149°C (300°F), for a period of time of about 3 minutes.
  • the gelled wear layer is then mechanically embossed with a fine overall pattern of a parchment paper-like texture in a Watson-Stillman Press for about 2 minutes under a pressure of about 0,959 MPa (140 psig) and at an elevated temperature created in the wear layer of just over 149°C (300°F).
  • the heated embossing takes place, along with the polymerization and/or cross-linking of the trimethylolpropane trimethacrylate in the wear layer but only in those portions thereof lying directly over the dicumyl peroxide, whereas there is substantially no polymerization and/or cross-linking to any significant or substantial degree in those other areas of the wear layer not lying directly over the dicumyl peroxide.
  • the melt viscosity of the wear layer portions lying over the dicumyl peroxide is materially increased, whereas the melt viscosity of the wear layer portions not lying over the dicumyl peroxide is substantially unchanged.
  • the mechanically embossed material is then heated in a fusion oven maintained at an elevated temperature of about 201,7°C (395°F), for about 2-3/4 minutes. Fusion of the resins takes place, along with the blowing and foaming of the potentially foamable plastisol in those areas not lying directly under the trimellitic anhydride inhibitor in the printing ink composition. There is very little blowing or foaming in the areas lying directly under the trimellitic anhydride.
  • the chemical embossing differential effect is excellent.
  • the elevated portions or lands of the wear layer develop a sleek, glossy or lustrous finish or texture, with high brilliance and sheen, whereas the lower or depressed portions or mortars retain the flat, dead or dull mat finish created therein by the mechanical embossing in the Watson-Stillman Press.
  • the appearance of the material, after the blowing or foaming cycle is very much like that of a glossy, glazed ceramic tile of high sheen, surrounded by a flat, dead or dull mat finish giving the appearance of grout or other cementitious material between the ceramic tiles.
  • the different colors of the printed pattern or design of the printing ink composition are in complete and perfect registry with (1) the above-described mechanical embossing effects of the contrasting sleek, glossy or lustrous areas and the flat, dead or dull areas, as well as (2) the above-described chemical embossing effect of higher and lower areas on the surface of the wear layer.
  • melt viscosity determinations for the relatively high polymerized and cross-linked portions and the relatively lowly polymerized and un-cross-linked portions of the resinous wear layer it has been established that the following melt viscosity ranges are suitable for the application of the principles of the present inventive concept.
  • the torque readings for the highly cross-linked portions of the wear layer should be in the range of from about 1000 to about 4000 meter-grams and the torque readings for the relatively un-cross-linked portions should be in the range of from about 300 to about 900, with differences in the torque readings for the two contrasting portions in the same product being at least about 250 meter grams.
  • cross-linked polymeric materials refers solely to the polymerization and cross-linking of the poly-functional reactive polymerizable monomeric materials, such as the trimethylolpropane trimethylacrylate, for example, in the resinous wear layer, which, of course, is cross-linked and thermoset.
  • the main resin in the wear layer is substantially uniformly and homogeneously distributed therein and is in a fused and polymerized state. However, it is not cross-linked and is still in a thermoplastic state, as compared to the cross-linked and thermoset polyfunctional polymeric materials in those portions of the wear layer lying over the polymerization or cross-linking initiator or organic peroxide.
  • Brabender determinations are run on samples of the highly polymerized portions of the resinous wear layer and on the relatively unpolymerized portions of the resinous wear layer at 150°C., at a shear rate of 30 revolutions per minute for fifteen minutes at which time the 53-gram samples are at equilibrium.
  • a type 6 roller mixer measuring head is used to determine the melt rheology of the wear layer plastisols.
  • the highly polymerized portions of the resinous wear layer yield torque readings of 2510 meter grams, whereas the relatively unpolymerized portions yield readings of only 650 meter grams.
  • a resinous polymer sheet material such as is illustrated in Figure 7 of the drawings is made as follows:
  • the results obtained in this Example are generally comparable to the results obtained in Example I, with the exception that the resinous polymer sheet material of this Example is not chemically embossed and the blowing or foaming operation is substantially uniform in its effect whereby the surfaces of the wear layer are substantially level and of the same height.
  • the flat, dead or dull embossed mat finish and the sleek, glossy or lustrous finish lie substantially in the same level plane.
  • concentration of polymerized or cross-linked trimethylolpropane trimethacrylate it is relatively high in those areas lying over the dicumyl peroxide and relatively low in those areas not lying directly over the dicumyl peroxide.
  • the melt viscosities are again relatively higher and lower, as indicated in Example I. Bumps as shown in the drawings are discernible and felt by the "finger-test”.
  • Barrier coat BC-1 is used in order to insure that no gases developed during the blowing or foaming escape up into the wear layer.
  • a resinous polymer sheet material such as is illustrated in Figure 8 of the drawings is made as follows:
  • zones A are retained after the mechanical embossment and through the fusion heating at elevated temperatures.
  • texture in zones B is lost during the fusion heating at the elevated temperatures and the final appearance of such zones B is sleek, glossy and lustrous. Elevated or raised bumps shown in the drawings are detectible and felt by the "finger-test”. Inasmuch as no blowing or foaming is involved in this Example, no barrier coat is employed.
  • the polyfunctional reactive polymerizable monomeric material namely, the trimethylolpropane trimethacrylate
  • the trimethylolpropane trimethacrylate is polymerized and is cross-linked solely in those areas of the wear layer lying directly over the polymerization initiator, namely, the dicumyl peroxide.
  • the trimethylolpropane trimethacrylate is substantially unpolymerized and is not cross-linked.
  • Example I The procedures generally described in Example I are followed substantially as set forth therein with certain variations as follows: the P-1 potentially foamable plastisol composition is used; the wet thickness is about 0,475 mm (18.7 mils); gelling takes place in a heated air atmosphere at about 149°C (300°F), for 3 minutes; a BC-1 barrier coat is used and has a thickness of about 0,076 mm (3 mils); it is gelled in a heated air atmosphere at about 149°C (300°F)., for about 3 minutes; the printing ink composition is P-1 and contains dicumyl peroxide and trimellitic anhydride as the polymerization initiator or organic peroxide and the blow modifier or inhibitor respectively; the non-active printing ink composition contains no polymerization initiator or organic peroxide or any equivalent material; the resinous wear layer is a W-1 composition and contains trimethylolpropane trimethacrylate as the reactive polymerizable monomer; it is about 0,304 mm (12 mils) thick and is gelled in a heated
  • the results obtained in this Example are generally comparable to the results obtained in Example 1.
  • the relatively low, relatively unblown mortar areas have embossed, flat, dead or dull finishes or textures, whereas the relatively elevated, relatively blown land areas possess a sleek, glossy or lustrous surface.
  • the mortar areas have a relatively high concentration of polymerized cross-linked monomer and have a high melt viscosity.
  • the land areas have practically no concentrations of polymerized cross-linked monomer and have a relatively low melt viscosity.
  • the product is commercially acceptable as a resilient floor covering.
  • Example V The procedures set forth in Example V are followed substantially as described therein with the exception that the P-1 printing ink composition used therein is replaced by printing ink compositions P-7 through P-17, as described previously herein, as eleven additional Examples:
  • Example V The procedures described in Example V are followed substantially as described therein with the exception that the dicumyl peroxide polymerization initiator in the printing ink composition is replaced by: .
  • Example V The procedures set forth in Example V are followed substantially as described therein with the following exceptions, with respect to the printing ink compositions used therein, wherein printing ink compositions identified as P-2 through P-5 in the pertinent table are used:
  • Example V The procedures described in Example V are followed substantially as set forth therein with the exception that the wear layer composition W-1 used therein is replaced by wear layer compositions W-3, W-6, W-7, W-9, W-10 and W-12, as described in the pertinent table herein.
  • the results of these Examples are generally comparable to the results obtained in Example V with wear layer compositions W-1.
  • the contrast between the embossed, flat, dead or dull textured areas and the sleek, glossy or lustrous smooth finish areas is very pronounced.
  • the differences in polymerization and/or cross-linking of the reactive polymerizable monomers in the respective wear layers are marked and considerable.
  • the differences in the melt viscosities of the various areas of the wear layer is also observed and is marked and considerable.
  • the products are commerically acceptable as resilient floor coverings.
  • Example V The results of these Examples are generally comparable to the results obtained in Example V.
  • the polymerization and/or cross-linking and the increase in melt viscosity are as described therein, along with the contrasting flat, dead or dull textures areas and the sleek, glossy or lustrous areas.
  • Example II The results of this Example are generally comparable to the results obtained in Example I.
  • the differences in polymerization and/or cross-linking of the reactive polymerizable monomer and the difference in melt viscosities of the various portions of the wear layer are noted, along with the contrasting surfaces of a flat, dead or dull mat texture and a sleek, smooth, glossy or lustrous finish.
  • the product is commercially acceptable as a resilient floor covering. Similar to the product of Example I, the portion of the wear layer in the flat, dead or dull mat finish area is cross-linked and thermoset, whereas the portion of the wear layer in the sleek, smooth, glossy or lustrous finish areas is not cross-linked nor is it thermoset but is still thermoplastic.
  • Example V The procedures described in Example V are followed substantially as described therein with the exception that the barrier coat composition BC-1 which is used therein is replaced by the barrier coat composition BC-2, as previously described hereinbefore.
  • the results of this Example are generally comparable to the results obtained in Example V.
  • the thickness of the barrier coat is also 0,114 mm (4.5 mils).
  • Example V The procedures described in Example V are followed substantially as described therein with the exception that the thickness of the barrier coat is changed to 0,038 mm (1.5 mils), 0,1016 mm (4 mils), and 0,127 mm (5 rnils), rather than the 0,114 mm (4.5 mils) thickness it possessed in Example V.
  • the results of these Examples are generally comparable to the results obtained in Example V.
  • Example V The procedures described in Example V are followed substantially as set forth therein with the exception that the mechanical embossing takes place under applied pressures of 0,343 Mpa (50 psig), 0,60 Mpa (86 psig) and 0,685 Mpa (100 psig), rather than the applied pressure of 0,754 MPa (110 psig) as employed in Example V.
  • the results of these Examples are generally comparable to the results obtained in Example V.
  • the flat, dead or dull mat finish areas contain cross-linked and thermoset resin, whereas the sleek, smooth, glossy or lustrous finish areas contain un-cross-linked, thermoplastic resin.
  • Example V The procedures described in Example V are followed substantially as set forth therein with the exception that the conditions for the mechanical embossing of the resinous wear layer are changed to: 0,959 MPa (140 psig), at 182,2°C (360°F), for a period of time of about 15 seconds.
  • Example V The procedures described in Example V are followed substantially as set forth therein with the exception that the conditions for the mechanical embossing of the resinous wear layer are changed to: 0,60 MPa (86 psig), 157,2°C (315°F), for a period of time of about 2 minutes.
  • Example II The results of this Example are generally comparable to the results obtained in Example I.
  • the polymerized and cross-linked thermoset portions of the resinous wear layer which have the higher melt viscosity retain the surface features and characteristics of the coarsely-textured parchment-type release paper, whereas the un-cross-linked thermoplastic portions of the resinous wear layer become sleek, smooth and glossy and lustrous.
  • Example XLVII The procedures described in Example XLVII are followed substantially as set forth therein with the exception that the heated, pressure-applying embossing roll is engraved with very fine parallel lines, fifty lines to 2,54 cm (the inch), which create the flat, dead or dull mat texture or finish, and contain cross-linked, thermoset resin, in contrast to the sleek, smooth, glossy or lustrous portions which contain un-cross-linked thermoplastic resin.
  • the results of this Example are generally comparable to the results of Example XLVII.
  • the resinous polymer sheet material illustrated in Figures 2 and 3 generally is made by the following alternative "upside-down" procedure wherein the composition of the potentially foamable plastisol, the printing ink compositions, the barrier coat composition, and the wear layer composition are as described in Example V.
  • the resinous wear layer plastisol containing the reactive polymerizable monomer and while still in highly fluid form is cast upon the surface of a coarsely textured, parchment-type release paper to a depth of about 0,381 mm (15 mils).
  • the wear layer plastisol is sufficiently fluid as to flow into and completely fill all the irregular recesses of the release paper, thereby assuming the surface features and characteristics of the release paper.
  • the wear layer is then gelled at 149°C (300°F).
  • Various printing ink compositions some containing both dicumyl peroxide polymerization initiator and trimellitic anhydride blow modifier and others not containing any polymerization initiators or organic peroxides or any blow modifiers or inhibitors, are applied to various areas of the exposed face of the gelled wear layer in the desired pattern or design. The printing ink compositions are then dried.
  • a 0,076 mm (3-mil) barrier coat is applied and adhered to the printing ink compositions and is heated at a temperature of about 160°C (320°F), for a sufficient period of time to not only gel the resinous barrier coat but also to activate or decompose the dicumyl peroxide in the wear layer to polymerize and/or cross-link the reactive polymerizable monomers lying in the same vertical zones and to increase the melt viscosities of the resins in such vertical zones.
  • a base layer or substrate comprising a potentially foamable plastisol composition and an adhered fibrous sheet of felted asbestos fibers is then laminated to the gelled barrier coat by passage through a laminator device under pressure and at an elevated temperature.
  • the resulting laminated product is unitary and integral in structure.
  • the coarsely textured parchment-type release paper is then stripped from the wear layer whose surface is thus exposed and found to be correspondingly coarsely textured and parchment-like in appearance, possessing a flat, dead or dull texture all over its surface.
  • This laminated product is then passed through a heated fusion oven at temperatures of about 201,7°C (395°F), and the resins are fused along with the blowing and the foaming operation wherein the blowing and foaming agent and the blowing modifier or inhibitor carry out their previously described chemical embossing procedures.
  • the resulting blown product is generally similar and comparable to the product of Example V.
  • Those portions of the wear layer wherein the reactive polymerizable monomers are polymerized and/or cross-linked and also possess a higher melt viscosity retain their coarsely textured parchment-type, flat, dead or dull mat structure and appearance.
  • the surfaces are melted to form sleek, smooth, glossy or lustrous finishes, occurring during the blowing and the foaming operation.
  • the cross-linked portions are thermoset, whereas the portions which are not cross-linked are thermoplastic.
  • Example V The procedures described in Example V are followed substantially as set forth therein with the exception that cumene hydroperoxide which is a polymerization initiator or organic peroxide activatable or decomposable only at relatively high temperatures is additionally included in the resinous wear layer substantially uniformly in a concentration of about 7 parts by weight based on 100 parts of resin, phr.
  • cumene hydroperoxide which is a polymerization initiator or organic peroxide activatable or decomposable only at relatively high temperatures is additionally included in the resinous wear layer substantially uniformly in a concentration of about 7 parts by weight based on 100 parts of resin, phr.
  • the cumene hydroperoxide is not activated or decomposed during the gelling operations or during the mechanical embossing operations, at which time the dicumyl peroxide is activated or decomposed in the printing ink composition whereby certain selected portions of the wear layer become polymerized and/or cross-linked, and develop relatively high melt viscosities, as described in this specification and in Example V in greater detail.
  • the cumene hydroperoxide is subsequently activated or decomposed at the more elevated temperatures which are present during the fusion, blowing or foaming cycle, whereby the reactive polymerizable monomers in the remaining sleek, smooth, glossy or lustrous finish areas are polymerized and/or cross-linked at that time, along with the increase in the melt viscosities in such sleek, smooth, glossy or lustrous portions.
  • the softening, melting and flowing in such areas precedes the polymerization and/or cross-linking and increase in melt viscosities in such areas.
  • Gloss level measurements are obtained for the wear layer surfaces (both land and mortar areas) of various polyvinyl chloride resinous sheet materials which are made by hand-operated, manually controlled laboratory procedures at 60°, using a Gardner Laboratories glossmeter standardized to an appropriate gloss plate for the 60° meter. Such laboratory procedures are not as sophisticated or as refined as are commercial plant manufacturing procedures and occasional blisters and irregularities cause lower than normal gloss readings.
  • the various polyvinyl chloride resinous sheet materials are obtained by the procedures generally described in Example I, with any variations in such procedures being noted.
  • Gloss level measurements are obtained for the wear layer surfaces (both land and mortar) of various polyvinyl chloride resinous sheet materials which are made by automated, electronically-controlled commercial production plant procedures, at 60° using a Gardner Laboratories glossmeter standardized to an appropriate gloss plate for the 60° meter. Such commercial production plant procedures are very sophisticated and very refined and yield gloss level measurements higher than those obtained by laboratory procedures.
  • the various polyvinyl chloride resinous sheet materials are obtained by the procedures generally described in Example I, with any variations in such procedures being noted.
  • Hot melt viscosities for various polyvinyl chloride plastisols are obtained, employing the C. W. Brabender "Plasticorder" with a jacket temperature of 150°C - to equilibrium in fifteen minutes; a shear rate of thirty revolutions per minute; and a sample weight of 53 grams.
  • the reactive polymerizable monomeric materials and the organic peroxide or free-radical polymerization initiator are as indicated.
  • Monomer “A” is trimethylolpropane trimethacrylate; monomer “B” is 1,6-hexanediol dimethacrylate; and monomer “C” is pentaerythritol triacrylate.
  • the organic peroxide or free-radical polymerization initiator is 40% active dicumyl peroxide, supported on precipitated calcium carbonate.
  • the resin for the first two controls is 100 parts polyvinyl chloride resin.
  • the resin for the second two controls is 89.5 parts of polyvinyl chloride resin and 10.5 parts of polyvinyl chloride blending resin.
  • the resin for the second chart is 100 parts polyvinyl chloride resin. 53.3 parts per hundred resin plasticizer blend are used for the controls.
  • Example II The procedures set forth in Example I are followed substantially as described therein with the exceptions that a barrier coat or layer is used, as shown in Figure 9, and all the various colored portions and areas of the printing ink composition used in applying the desired pattern or design to the gelled and cooled resinous polymer plastisol composition have the following formulations containing the same concentrations and amounts of dicumyl peroxide polymerization initiator or catalyst:
  • Omission of the azodicarbonamide blowing or foaming agent (1.1 parts) from the formulation of the resinous polymer plastisol composition of Example I provides a final unblown or unfoamed product, such as illustrated in Figure 9, wherein the mechanical embossing is substantially completely retained throughout the heating and fusion, and blowing or foaming operations. In such a case where there is no blowing or foaming, the barrier coat or layer is eliminated.
  • Example I The procedures set forth in Example I are followed substantially as described therein, with the exception that none of the printing ink compositions contain any polymerization initiators, catalysts, or organic peroxides and have the following formulations:
  • a separate layer or coating such as a clear printing ink composition containing dicumyl peroxide polymerization initiator or catalyst is applied overall, as shown in the structure of the product illustrated in Figure 12.
  • a clear printing ink composition has the following formulation:
  • Example I The procedures set forth in Example I are followed substantially as described therein with the exceptions that a barrier coat or layer is used and none of the printing ink compositions have any polymerization initiators, catalysts, or organic peroxides therein.
  • Such printing ink compositions have the following formulations:
  • Example LV no separate overall layer or coating such as a clear printing ink composition containing any polymerization initiators, catalysts, or organic peroxides as is used in Example LV, is included in the structure of the product.
  • the product, immediately prior to the heating and fusion, and the blowing or foaming operation, is generally similar to the product which is illustrated in Figure 1 of the drawings. Subsequently, it is observed that the mechanical embossing on the surface of the wear layer is substantially retained completely through the heating and fusion, and the blowing or foaming operation.
  • Example I The procedures set forth in Example I are followed substantially as described therein with the exceptions that a barrier coat or layer is used and none of the printing ink compositions have any polymerization initiators, catalysts, or organic peroxides therein.
  • Such printing ink compositions have the formulations described in Example LVI.
  • Example LV no separate overall coating such as a clear printing ink composition containing any polymerization initiators, catalysts, or organic peroxides, as is used in Example LV is included in the structure of the product.
  • the product, immediately prior to the heating and fusion, and the blowing or foaming operation, is generally similar to the product which is illustrated in Figure 9 of the drawings except that the printing ink compositions contain no polymerization initiators, catalysts or organic peroxides. Subsequently, it is observed that the mechanical embossing on the surface of the wear layer is substantially retained completely through the heating and fusion, and the blowing or foaming operation.

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Laminated Bodies (AREA)
  • Printing Methods (AREA)
EP79100313A 1978-02-21 1979-02-02 Resinous polymer sheet materials having selective, surface decorative effects and methods of making the same Expired EP0003965B1 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US87917178A 1978-02-21 1978-02-21
US879171 1978-02-21
US94224678A 1978-09-14 1978-09-14
US942246 1978-09-14

Publications (2)

Publication Number Publication Date
EP0003965A1 EP0003965A1 (en) 1979-09-19
EP0003965B1 true EP0003965B1 (en) 1983-01-26

Family

ID=27128525

Family Applications (1)

Application Number Title Priority Date Filing Date
EP79100313A Expired EP0003965B1 (en) 1978-02-21 1979-02-02 Resinous polymer sheet materials having selective, surface decorative effects and methods of making the same

Country Status (15)

Country Link
EP (1) EP0003965B1 (es)
JP (1) JPS5835873B2 (es)
AU (1) AU512127B2 (es)
BR (1) BR7901058A (es)
DE (1) DE2964579D1 (es)
ES (1) ES477875A1 (es)
HU (1) HU181863B (es)
IE (1) IE47809B1 (es)
IL (1) IL56537A (es)
MX (1) MX151304A (es)
NO (1) NO790276L (es)
NZ (1) NZ189540A (es)
PH (1) PH15917A (es)
PL (1) PL121885B1 (es)
RO (1) RO80313A (es)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6555216B2 (en) 1997-02-20 2003-04-29 Mannington Mill, Inc. Contrasting gloss surface coverings optionally containing dispersed wear-resistant particles and methods of making the same

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4603074A (en) * 1985-05-22 1986-07-29 Gencorp Inc. Vinyl chloride polymer laminate
US7014802B1 (en) 1997-02-20 2006-03-21 Mannington Mills, Of Delaware, Inc. Methods to make a surface covering having a natural appearance
US6114008A (en) * 1997-02-20 2000-09-05 Mannington Mills, Inc. Surface coverings having a natural appearance and methods to make a surface covering having a natural appearance
US5961903A (en) * 1997-02-20 1999-10-05 Mannington Mills, Inc. Method of making a surface covering having a natural appearance
US7081291B2 (en) 2002-01-11 2006-07-25 Domco Tarkett Inc. Selectively embossed surface coverings and processes of manufacture
US8969514B2 (en) 2007-06-04 2015-03-03 Synergy Pharmaceuticals, Inc. Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases
CN117926991A (zh) * 2016-07-18 2024-04-26 博优国际集团公众有限公司 呈现出三维浮雕和装饰图像的适合作为地板或墙壁覆盖物的多层片材

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3519527A (en) * 1966-04-08 1970-07-07 Richard P Crowley Embossed plastic surface coverings and method of preparing same
US3544490A (en) * 1967-01-04 1970-12-01 Gulf Research Development Co Ethylene polymer foam compositions and process for making same
US3821059A (en) * 1972-04-05 1974-06-28 Armstrong Cork Co Segmentally accommodating loose-lay floor
US3870591A (en) * 1972-06-27 1975-03-11 Armstrong Cork Co Dimensionally stable, flexible plastic surface coverings
JPS4933107A (es) * 1972-07-30 1974-03-27
JPS5230617B2 (es) * 1973-07-20 1977-08-09
JPS51495A (en) * 1974-06-19 1976-01-06 Glory Kogyo Kk Shoruiketsusokukino shidoseigyosochi
JPS5139561A (ja) * 1974-10-01 1976-04-02 Aida Eng Ltd Kinzokufunmatsuseizosochi
US3958043A (en) * 1974-11-19 1976-05-18 Armstrong Cork Company Method of making chemically embossed surface coverings
JPS5210153A (en) * 1975-07-14 1977-01-26 Yoshihiro Hata Folding glasses
US4113487A (en) * 1975-10-31 1978-09-12 Toppan Printing Co., Ltd. Method for manufacture of expanded articles having an embossed surface

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6555216B2 (en) 1997-02-20 2003-04-29 Mannington Mill, Inc. Contrasting gloss surface coverings optionally containing dispersed wear-resistant particles and methods of making the same

Also Published As

Publication number Publication date
AU4408379A (en) 1979-09-27
DE2964579D1 (en) 1983-03-03
JPS54123310A (en) 1979-09-25
IE47809B1 (en) 1984-06-27
IE790193L (en) 1979-08-21
BR7901058A (pt) 1979-10-02
PL213594A1 (pl) 1979-12-17
RO80313A (ro) 1982-12-06
AU512127B2 (en) 1980-09-25
MX151304A (es) 1984-11-08
IL56537A (en) 1982-07-30
EP0003965A1 (en) 1979-09-19
NZ189540A (en) 1981-04-24
HU181863B (en) 1983-11-28
PL121885B1 (en) 1982-06-30
JPS5835873B2 (ja) 1983-08-05
NO790276L (no) 1979-08-22
PH15917A (en) 1983-04-22
IL56537A0 (en) 1979-03-12
ES477875A1 (es) 1980-04-01

Similar Documents

Publication Publication Date Title
US4187131A (en) Resinous polymer sheet materials having selective, surface decorative effects and methods of making the same
US4214028A (en) Resinous polymer sheet materials having surface decorative effects and methods of making the same
US4248922A (en) Resinous polymer sheet materials having selective, surface decorative effects and methods of making the same
US4217385A (en) Resinous polymer sheet materials having selective, surface decorative effects and methods of making the same
US4273819A (en) Differential gloss products and methods of making the same
US4844849A (en) Method of making embossed decorative sheets
US4491616A (en) Resinous polymer sheet material having surface decorative effects of contrasting gloss and method of making the same
US4068030A (en) Multilevel embossing by printing with a reactive monomer
US2918702A (en) Method of producing resilient plastic surface covering
US3399106A (en) Embossed resinous compositions and process for preparing same
NO740375L (es)
US3224894A (en) Process for producing decorative surface covering
US3870591A (en) Dimensionally stable, flexible plastic surface coverings
US4298646A (en) Differential gloss products and methods of making the same
US3196030A (en) Decorative foam surface covering and process therefor
US3574659A (en) Process of textured resinous sheet preparation
JPS61102251A (ja) 化粧積層品
US3278322A (en) Process for producing a decorative surface covering
EP0003965B1 (en) Resinous polymer sheet materials having selective, surface decorative effects and methods of making the same
JPH06226921A (ja) 化粧表面カバー
EP0192218B1 (en) Printable composition for making embossed decorative sheets
US3265548A (en) Processes for preparing decorative surface coverings
US3343975A (en) Process of producing decorative surface covering
CA1195558A (en) Differential gloss products and methods of making the same
CA1114608A (en) Resinous polymer sheet materials having selective, surface decorative effects and methods of making the same

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Designated state(s): BE CH DE FR GB IT NL SE

ITCL It: translation for ep claims filed

Representative=s name: ING. C. GREGORJ S.P.A.

17P Request for examination filed
DET De: translation of patent claims
ITF It: translation for a ep patent filed

Owner name: ING. C. GREGORJ S.P.A.

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Designated state(s): BE CH DE FR GB IT NL SE

REF Corresponds to:

Ref document number: 2964579

Country of ref document: DE

Date of ref document: 19830303

ET Fr: translation filed
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: CH

Payment date: 19840113

Year of fee payment: 6

REG Reference to a national code

Ref country code: CH

Ref legal event code: PUE

Owner name: CONGOLEUM CORPORATION

REG Reference to a national code

Ref country code: GB

Ref legal event code: 732

REG Reference to a national code

Ref country code: FR

Ref legal event code: TP

NLS Nl: assignments of ep-patents

Owner name: CONGOLEUM CORPORATION (1984 DELAWARE CORPORATION)

ITPR It: changes in ownership of a european patent

Owner name: CESSIONE;CONGOLEUM CORPORATION

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CH

Effective date: 19880229

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 19920131

Year of fee payment: 14

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: BE

Payment date: 19920212

Year of fee payment: 14

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 19930108

Year of fee payment: 15

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SE

Payment date: 19930125

Year of fee payment: 15

Ref country code: FR

Payment date: 19930125

Year of fee payment: 15

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Effective date: 19930228

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 19930228

Year of fee payment: 15

BERE Be: lapsed

Owner name: CONCOLEUM CORP.

Effective date: 19930228

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Effective date: 19931103

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Effective date: 19940202

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Effective date: 19940203

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Effective date: 19940901

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 19940202

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Effective date: 19941031

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

EUG Se: european patent has lapsed

Ref document number: 79100313.0

Effective date: 19940910

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT