US3185582A - Process for making and finishing artificial hides or leathers - Google Patents

Process for making and finishing artificial hides or leathers Download PDF

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US3185582A
US3185582A US92170A US9217061A US3185582A US 3185582 A US3185582 A US 3185582A US 92170 A US92170 A US 92170A US 9217061 A US9217061 A US 9217061A US 3185582 A US3185582 A US 3185582A
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lap
latex
bonded
water
water content
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US92170A
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Alegre Antonio Albareda
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Priority to DENDAT1288061D priority Critical patent/DE1288061B/de
Priority to FR1115866D priority patent/FR1115866A/en
Priority to FR1115864D priority patent/FR1115864A/en
Priority to DEA21751A priority patent/DE1204618B/en
Priority to US92170A priority patent/US3185582A/en
Application filed by Individual filed Critical Individual
Priority to FR888990A priority patent/FR81199E/en
Priority to GB7777/62A priority patent/GB992261A/en
Priority to NL275386A priority patent/NL126058C/xx
Priority to ES0275317A priority patent/ES275317A1/en
Application granted granted Critical
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Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/12Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins
    • CCHEMISTRY; METALLURGY
    • C14SKINS; HIDES; PELTS; LEATHER
    • C14CCHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
    • C14C11/00Surface finishing of leather
    • C14C11/003Surface finishing of leather using macromolecular compounds
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/58Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
    • D04H1/64Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives the bonding agent being applied in wet state, e.g. chemical agents in dispersions or solutions
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/0056Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the compounding ingredients of the macro-molecular coating
    • D06N3/0061Organic fillers or organic fibrous fillers, e.g. ground leather waste, wood bark, cork powder, vegetable flour; Other organic compounding ingredients; Post-treatment with organic compounds
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/04Artificial 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
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/04Artificial 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
    • D06N3/10Artificial 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 styrene-butadiene copolymerisation products or other synthetic rubbers or elastomers except polyurethanes
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/904Artificial leather

Definitions

  • the present invention relates to a process for making and finishing artificial hides or leathers.
  • the main object of this invention is to produce a material having characteristics similar to natural leather.
  • Porosity is a distinctive feature of natural leather and is the feature of natural leather which makes same preferred over plastic materials for many uses. I have found that by bonding and coating natural or synthetic fibers with a natural or synthetic latex, in the hereinafter described manner, useful materials can be attained, the characteristics or" feel and porosity of which are practically the same as those of natural leather.
  • textile fibers such as cotton, rayon, nylon, acetated fibers, etc., and their waste or combinations of same, are formed into Webs, e.g., in a carding engine, and by laying the Webs one over the other a lap is made of the desired thickness.
  • This lap may also be prepared in a machine commonly called a Curlator.
  • the lap of the desired thickness is dipped into a latex bath which is characterized by the ability to coagulate at atemperature in the range of from about 60 to about 80 C. and is of approximately the following composition:
  • the latex-impregnated lap obtained from the immersion in the latex bath then is heated to a temperature in the range of from about 60 to about 80 C. for a time period requisite to effect the coagulation of the latex and to bond the fibers of the lap together.
  • Any suitable means can be employed to effect the coagulation-efiecting heating of the lap.
  • the lateximpregnated lap is passed continuously through an oven, the inside temperature of whichis maintained at about 200 to 300 C., at a rate which allows the latex-impregnated lap to be heated to the aforementioned latexcoagulation conditions.
  • Coagulation can also be obtained by means of dielectric heating, hot contact, or infrared rays, etc. The object of the invention is not affected by the means for heating the impregnated lap.
  • a latex bath having substantially the above-characteristics is employed in order to achieve a final leather-like product of uniform properties.
  • Latices which coagulate much below 60 C., e.g., at about 40 C., are difficult to utilize in that premature coagulation in the latex bath preliminary to 3,185,582 Patented May 25, 1965 the impregnation of the lap is a problem.
  • latices which coagulate at much above 80 C. e.g., at about 95 C.
  • the increased tendency of water in the latex-impregnated lap to evaporate sets up convection currents in the latex solids dispersion which causes rubber particles therein to tend to migrate to the surface of the impregnated lap and coagulate there.
  • This migration deprives the fibers located within the interior of the lap of intended bonding material, whereby an inferior product which is likely to delaminate is obtained.
  • the impregnated lap loses part of its water by evaporation, but it still contains an appreciable proportion of that initially present, e.g., about 100 to about 300% by weight, based on the dry weight of the bonded lap, and the resultant water-containing bonded lap is squeezed through rolls or by press, neither the rolls nor the press being heated, to reduce the water content of the bonded lap, after which operation the material of reduced water content is dried at a temperature not above 120 C.
  • the material after squeezing and before drying, shall contain an amount of water of from to 50% of the total weight of such material so that, upon the evaporation of the water in the drying step, the spaces occupied by the water in said bonded material of reduced water content are superseded by air cells which, in the resultant dry artificial leather product, impart to it the characteristic of porosity.
  • the porous, bonded material when it is dry it is coated by means of aerographing, brushing, calender spreading or analogous methods, the coating, or paint, being prepared with casein containing plasticizers such as sulphoricina-ted oil, glycerine, dibutyl phthalate, etc., pigments to impart the desired color such as synthetic iron oxides, loading or filling materials to provide appropriate feel, such as titanium dioxide, lithopone, barium chloride, barium sulphate,
  • Coating materials prepared with the foregoing elements lack bonding power and resistance in order to avoid premature aging; and their abrasive resistance also usually has to be increased. All of these necessary properties are obtained by adding to the said coating materials aqueous dispersions of resins such as acrylonitrilebutadiene copolymers, butadiene-styrene copolymers, polyvinyl chloride, polymethyl-methacrylate, other poly- 1 meric derivatives of the acrylates, mixtures of said resins,
  • resins such as acrylonitrilebutadiene copolymers, butadiene-styrene copolymers, polyvinyl chloride, polymethyl-methacrylate, other poly- 1 meric derivatives of the acrylates, mixtures of said resins,
  • composition An example of a coating mixture, or paint, employed in the present invention may be prepared according to the following composition:
  • Pigments for example, synthetic iron oxides,
  • Dibutyl phthalate 20 to 35 After applying one coat of the paint on the porous artificial leather, another coat is applied, or two or three as circumstances require, in the latter instances with a paint similar to that described above but free of Wetting agent and characterized by a substantial or total reduction in glycerine or dibutyl phthalate content. As the coats are applied they are dried. When these coats are dry a lustre coat is applied which may be as follows:
  • Casein Parts by weight (dry) Casein (dissolved in water, 15 100 Resin (any one or a combination of those given above) 50 Plasticizer (sulphoricinated oil, for example) 25 to 60 Approximately 2% of formaldehyde or other antiferment is added to all these compositions to avoid posterior decomposition of the casein.
  • the lustre coating is dry, the resulting coated material is treated again with a 15% to 20% formaldehyde solution and thereafter dried at room temperature or in a drying chamber with hot air at 50 to 80 C. After such drying, the material is ironed at 70 to 80 C. for 5 to 30 seconds at a pressure of approximately from about 25 to about 50 kgs./cm
  • a coating e.g., based primarily on plasticized polyvinyl chloride free of casein, is applied to the porous, dry bonded lap prepared by the aforementioned impregnating, coagulating, squeezing and drying steps to provide an excellent leatherlike product.
  • polyvinyl chloride coating layer is the following:
  • the latex contained in the agglomerating mixture present in the impregnated fiber lap is coagulated by means of heat, and then the material is squeezed, eliminating water contained in the coagulated mass in a proportion which may represent from one to three times the weight of the artificial leather in dry condition.
  • the material After squeezing, the material must still contain from 20 to 50% of its weight in water.
  • the pressure exerted by the press or squeezing cylinders for squeezing the material after coagulation has to be adjusted so as to leave in the material a water content varying from 20 to 50% of the Weight of the material, according to the end uses for which the artificial leather is intended.
  • the material is dried, and once the drying is totally completed the material is suitable for receiving a coating of a weight ranging from 70 to 300 grams per square meter, approximately, and
  • the ultimate use of the artifical leather of the present invention does not necessarily require that it be porous, over the first PVC coating which is perfectly anchored on the agglomerated fibers to provide a material possessing the precisely desired degree of porosity, other coating layers may be applied, thus increasing the thickness thereof as desired.
  • a method for producing a substitute leather from a lap of fibers comprising impregnating said lap with a latex selected from the group consisting of natural latex, synthetic latex, and mixtures thereof, heating the resultant latex-impregnated lap at a temperature in the range of from about 60 to about C.
  • a method for producing a substitute leather from a lap of fibers consisting of impregnating said lap with a latex, heating the impregnated lap at a temperature in the range of from about 60 to about 80 C. for a time period sutiicient to coagulate the latex and bind the fibers of the lap together and to produce a bonded lap containing water in an amount appreciably above 50% by weight of said latex-impregnated lap, squeezing said water-containing bonded lap to reduce the water content thereof to a level in the range of from about 20 to about 50% by weight based on the dry weight of the lap, drying the resulting bonded lap of reduced water content at a temperature of about C.
  • said latex is selected from the group consisting of natural latex, synthetic latex, and mixtures thereof.
  • a method for producing a substitute leather from a lap of fibers consisting of impregnating said lap with a latex selected from the group consisting of natural latex, synthetic latex, and mixtures thereof,
  • resultingporous, dry lap with a plurality of coats including a first coat, intermediate coats, and a final coat,,of a resinous dispersion mixture comprising casein, a polymer selected from the group consisting of butadiene-styrene, butadiene-acrylonitrile, polyvinyl chloride, methylmethacrylate, and mixtures thereof, and pigments, fillers, and at least one plasticizer heating the coated lap after each coating to a temperature sufiicient to dry thecoating material and thereby provide a producthaving substantially the porosity of a similarly coated natural leather.
  • a resinous dispersion mixture comprising casein, a polymer selected from the group consisting of butadiene-styrene, butadiene-acrylonitrile, polyvinyl chloride, methylmethacrylate, and mixtures thereof, and pigments, fillers, and at least one plasticizer heating the coated lap after each coating to a temperature sufiicient to dry theco
  • a method for producinga substitute leather from a lap of fibers consisting of impregnating said lap with latex, heating the impregnated lap at a temperature in the range of about 60 to about 80 C. for a time period suflicient to coagulate the latex and bind the fibersof the lap together and, to produce a bonded lap containing Water in an amount appreciably above 50% by weight of said latex-impregnated lap, squeezing said water-containing bonded lap to reduce the water content" thereof toa level in the range of about 20 to about 50% by Weight based on the dry lap, drying the resulting bonded lap-of reduced water content at a temperature of about 120 coating material is deposited on said lap in a total amount C.
  • said latex is selected from the group consisting of natural latex, synthetic latex and mixtures thereof.

Description

United States Patent '0 "ice 3,185,582 PROCESS FOR MAKING AND FlNlSHlNG .ARTHECIAL HIDES R LEATHERS Antonio Albareda Alegre, 5 Jose Bertrand St, Barcelona, Spain No Drawing. Filed Feb. 28, 1961, Ser. No. 92,170 Claims priority, application Spain, Dec. 17, 1953,
9 Claims. (Cl. 117-11 The present invention relates to a process for making and finishing artificial hides or leathers.
This application is a continuation-in part of my copending application Serial No. 475,318, filed December 14, 1954. t
The main object of this invention is to produce a material having characteristics similar to natural leather. Porosity is a distinctive feature of natural leather and is the feature of natural leather which makes same preferred over plastic materials for many uses. I have found that by bonding and coating natural or synthetic fibers with a natural or synthetic latex, in the hereinafter described manner, useful materials can be attained, the characteristics or" feel and porosity of which are practically the same as those of natural leather.
In accordance with the process of this invention, textile fibers, such as cotton, rayon, nylon, acetated fibers, etc., and their waste or combinations of same, are formed into Webs, e.g., in a carding engine, and by laying the Webs one over the other a lap is made of the desired thickness. This lap may also be prepared in a machine commonly called a Curlator. Then, in a continuous system, the lap of the desired thickness is dipped into a latex bath which is characterized by the ability to coagulate at atemperature in the range of from about 60 to about 80 C. and is of approximately the following composition:
. Parts by weight (dry) Natural or synthetic latex of approximately In accordance with the present method, the latex-impregnated lap obtained from the immersion in the latex bath then is heated to a temperature in the range of from about 60 to about 80 C. for a time period requisite to effect the coagulation of the latex and to bond the fibers of the lap together. Any suitable means can be employed to effect the coagulation-efiecting heating of the lap. In one technique of the heating step, the lateximpregnated lap is passed continuously through an oven, the inside temperature of whichis maintained at about 200 to 300 C., at a rate which allows the latex-impregnated lap to be heated to the aforementioned latexcoagulation conditions. Coagulation can also be obtained by means of dielectric heating, hot contact, or infrared rays, etc. The object of the invention is not affected by the means for heating the impregnated lap.
In accordance with the invention, a latex bath having substantially the above-characteristics is employed in order to achieve a final leather-like product of uniform properties. Latices which coagulate much below 60 C., e.g., at about 40 C., are difficult to utilize in that premature coagulation in the latex bath preliminary to 3,185,582 Patented May 25, 1965 the impregnation of the lap is a problem. On the other hand, latices which coagulate at much above 80 C., e.g., at about 95 C., suffer from the disadvantage that during the coagulation heating step the increased tendency of water in the latex-impregnated lap to evaporate sets up convection currents in the latex solids dispersion which causes rubber particles therein to tend to migrate to the surface of the impregnated lap and coagulate there. This migration deprives the fibers located within the interior of the lap of intended bonding material, whereby an inferior product which is likely to delaminate is obtained.
In the method of this invention, during the heating step for coagulating the latex in the latex-impregnated lap, the impregnated lap loses part of its water by evaporation, but it still contains an appreciable proportion of that initially present, e.g., about 100 to about 300% by weight, based on the dry weight of the bonded lap, and the resultant water-containing bonded lap is squeezed through rolls or by press, neither the rolls nor the press being heated, to reduce the water content of the bonded lap, after which operation the material of reduced water content is dried at a temperature not above 120 C. For the implementation of the present invention, it is indispensable that the material, after squeezing and before drying, shall contain an amount of water of from to 50% of the total weight of such material so that, upon the evaporation of the water in the drying step, the spaces occupied by the water in said bonded material of reduced water content are superseded by air cells which, in the resultant dry artificial leather product, impart to it the characteristic of porosity.
In one embodiment of the present invention, when the porous, bonded material is dry it is coated by means of aerographing, brushing, calender spreading or analogous methods, the coating, or paint, being prepared with casein containing plasticizers such as sulphoricina-ted oil, glycerine, dibutyl phthalate, etc., pigments to impart the desired color such as synthetic iron oxides, loading or filling materials to provide appropriate feel, such as titanium dioxide, lithopone, barium chloride, barium sulphate,
kaolin or bentonite, etc.
Coating materials prepared with the foregoing elements lack bonding power and resistance in order to avoid premature aging; and their abrasive resistance also usually has to be increased. All of these necessary properties are obtained by adding to the said coating materials aqueous dispersions of resins such as acrylonitrilebutadiene copolymers, butadiene-styrene copolymers, polyvinyl chloride, polymethyl-methacrylate, other poly- 1 meric derivatives of the acrylates, mixtures of said resins,
and other resins of similar effects.
An example of a coating mixture, or paint, employed in the present invention may be prepared according to the following composition:
Parts by weight (dry) Resins (anyone or combination of those given above) Casein (15% solution in ammonia) 15 to 100 Filler (those previously mentioned, for example,
titanium dioxide, lithopone, barium chloride,
etc.) Pigments (for example, synthetic iron oxides,
Dibutyl phthalate 20 to 35 After applying one coat of the paint on the porous artificial leather, another coat is applied, or two or three as circumstances require, in the latter instances with a paint similar to that described above but free of Wetting agent and characterized by a substantial or total reduction in glycerine or dibutyl phthalate content. As the coats are applied they are dried. When these coats are dry a lustre coat is applied which may be as follows:
Parts by weight (dry) Casein (dissolved in water, 15 100 Resin (any one or a combination of those given above) 50 Plasticizer (sulphoricinated oil, for example) 25 to 60 Approximately 2% of formaldehyde or other antiferment is added to all these compositions to avoid posterior decomposition of the casein. When the lustre coating is dry, the resulting coated material is treated again with a 15% to 20% formaldehyde solution and thereafter dried at room temperature or in a drying chamber with hot air at 50 to 80 C. After such drying, the material is ironed at 70 to 80 C. for 5 to 30 seconds at a pressure of approximately from about 25 to about 50 kgs./cm
In certain of such embodiments of the invention, excellent results are obtained by reducing the amount of the filler and increasing the proportion of zinc stearate. The articles thus produced are characterized, on rubbing, by a natural gloss which is hardly distinguishable from that of natural leather. This is why in the basic mixture of the foregoing examples a proportion of zinc stearate ranging broadly from 10 to 200 parts is mentioned. When proportions of zinc stearate of from 50 to 150 parts are used, the percentages of fillers referred to, i.e., lithopone, titanium dioxide, barium chloride, etc., are totally or nearly totally suppressed.
In another embodiment of the present invention, a coating, e.g., based primarily on plasticized polyvinyl chloride free of casein, is applied to the porous, dry bonded lap prepared by the aforementioned impregnating, coagulating, squeezing and drying steps to provide an excellent leatherlike product.
An example of the polyvinyl chloride coating layer is the following:
Parts Polyvinyl chloride From 55 to 62 Dioctyl phthalate From 12 to '16 Dioctyl adipate From 12 to 16 Filler (for instance, CaCO From to 12 Epoxy resin (plasticizer) From 1 to 3 Pigments From 1 to 4 Cadmium barium laurate From 0.25 to 0.75 Epoxy resin (synergistic stabilizer) From 1 to 2 After coating, the resultant material is heated at a temperature of 170 C. for approximately from 2 to 5 minutes so that gelification of the coating is produced, then the material is pressed and eventually engraved.
With the method of my invention, the latex contained in the agglomerating mixture present in the impregnated fiber lap is coagulated by means of heat, and then the material is squeezed, eliminating water contained in the coagulated mass in a proportion which may represent from one to three times the weight of the artificial leather in dry condition. After squeezing, the material must still contain from 20 to 50% of its weight in water. The pressure exerted by the press or squeezing cylinders for squeezing the material after coagulation has to be adjusted so as to leave in the material a water content varying from 20 to 50% of the Weight of the material, according to the end uses for which the artificial leather is intended.
After the squeezing step the material is dried, and once the drying is totally completed the material is suitable for receiving a coating of a weight ranging from 70 to 300 grams per square meter, approximately, and
by means of such a coating layer a finish very similar to that of natural leather is obtained, with the coated material retaining practically all the porosity necessary for it being a suitable leather substitute.
By means of the present invention the troublesome industrial processes devised for imparting porosity to PVC films or other plastic coatings, which processes entail a piercing technique, are avoided.
If the ultimate use of the artifical leather of the present invention does not necessarily require that it be porous, over the first PVC coating which is perfectly anchored on the agglomerated fibers to provide a material possessing the precisely desired degree of porosity, other coating layers may be applied, thus increasing the thickness thereof as desired.
- With either of the two described methods, artificial hides and leathers having porous and resistant finishes are obtained which are excellently adapted for use in industries and applications such as footwear and upholstery requiring the porosity or finish of natural hides or leathers.
I claim:
1. A method for producing a substitute leather from a lap of fibers comprising impregnating said lap with a latex selected from the group consisting of natural latex, synthetic latex, and mixtures thereof, heating the resultant latex-impregnated lap at a temperature in the range of from about 60 to about C. for a time period requisite to coagulate said latex and bind the fibers of said lap together and to produce a bonded lap containing Water in an amount appreciably above 50% by weight of said latex-impregnated lap, thereafter squeezing said Water-containing bonded lap to reduce the water content thereof to a level in the range of from about 20 to about 50% by weight based on the dry Weight of the lap, and then drying the resulting bonded lap of reduced water content at a temperature of about 120 C. to provide a porous, bonded lap having free spaces therewithin corresponding essentially to those spaces occupied by said water present in said bonded lap of reduced water content preliminary to said drying step.
2. The method according to claim 1 wherein the water content of said water-containing bonded lap, preliminary to said squeezing step, is in the range of from about to about 300% by weight.
3. A method for producing a substitute leather from a lap of fibers, said method consisting of impregnating said lap with a latex, heating the impregnated lap at a temperature in the range of from about 60 to about 80 C. for a time period sutiicient to coagulate the latex and bind the fibers of the lap together and to produce a bonded lap containing water in an amount appreciably above 50% by weight of said latex-impregnated lap, squeezing said water-containing bonded lap to reduce the water content thereof to a level in the range of from about 20 to about 50% by weight based on the dry weight of the lap, drying the resulting bonded lap of reduced water content at a temperature of about C. to provide a porous bonded lap having free spaces therewithin corresponding essentially to those spaces occupied by said water present in said bonded lap of reduced water content preliminary to said drying step, coating the resulting porous, dry lap with at least one coat of a mixture comprising a polyvinyl chloride, a polymer selected from the group consisting of butadiene-acrylonitrile, butadienestyrene, methylmethacrylate and mixtures thereof, and pigments, stabilizers, fillers, and at least one plasticizer, and heating the coated lap after each coating to a temperature sufiicient to gel the coating material, and eventually pressing and engraving the coated lap to thereby provide a product having substantially the porosity and aspect of natural leather.
4. The process in accordance with claim 3, wherein said latex is selected from the group consisting of natural latex, synthetic latex, and mixtures thereof.
5. A method for producing a substitute leather from a lap of fibers, said method consisting of impregnating said lap with a latex selected from the group consisting of natural latex, synthetic latex, and mixtures thereof,
heating the impregnated lap to coagulate the latex and bind the fibers of the lap together and to provide a bonded lap containing water in an amount appreciably above 50% by Weight of said latex-impregnated lap, squeezing said Water-containing bonded lap to reduce the Water content thereof to a level inthe range of from about 20 to about 50% by weightbasedcon the dry lap, drying the resulting bonded lap of reduced water content at a temperature of about 120 C. to provide a porous, bonded lap having free spaces therewithin corresponding essentially tothose spaces occupied by said water present in said bonded lap of reduced water content preliminary to said drying step, coating the. resultingporous, dry lap with a plurality of coats, including a first coat, intermediate coats, and a final coat,,of a resinous dispersion mixture comprising casein, a polymer selected from the group consisting of butadiene-styrene, butadiene-acrylonitrile, polyvinyl chloride, methylmethacrylate, and mixtures thereof, and pigments, fillers, and at least one plasticizer heating the coated lap after each coating to a temperature sufiicient to dry thecoating material and thereby provide a producthaving substantially the porosity of a similarly coated natural leather.
6. A method for producinga substitute leather from a lap of fibers consisting of impregnating said lap with latex, heating the impregnated lap at a temperature in the range of about 60 to about 80 C. for a time period suflicient to coagulate the latex and bind the fibersof the lap together and, to produce a bonded lap containing Water in an amount appreciably above 50% by weight of said latex-impregnated lap, squeezing said water-containing bonded lap to reduce the water content" thereof toa level in the range of about 20 to about 50% by Weight based on the dry lap, drying the resulting bonded lap-of reduced water content at a temperature of about 120 coating material is deposited on said lap in a total amount C. to provide a porous, bonded lap having free spaces therewithin corresponding essentially to those spaces occupied by said water present in said bonded lap of reduced water content preliminary to said drying step, coating the resulting porous, dry lap with at least one coat containing polyvinyl chloride, fillers, stabilizers, pigments, and a plasticizer, and heating the resulting coated lap after each coating to a temperature sufficient to gel the material in the coating, thereby providing a product having substantially the porosity of natural leather.
7. The process according to claim 6 wherein said latex is selected from the group consisting of natural latex, synthetic latex and mixtures thereof.
8. The process in accordance with claim 6 wherein said coated lap is heatedat 170 C. for from 2 to 5 minutes after each coating.
9. The process in accordance with claim 6 wherein said of from 70 to 300 grams per square meter.
References Cited by the Examiner UNITED STATES PATENTS RICHARD D. NEVIUS, Primary Examiner.
JOSEPH REBOLD, Examiner.

Claims (1)

1. A METHOD FOR PRODUCING A SUBSTITUTE LEATHER FROM A LAP OF FIBERS COMPRISING IMPREGNATING SAID LAP WITH A LATEX SELECTED FROM THE GROUP CONSISTING OF NATURAL LATEX, SYNTHETIC LATEX, AND MIXTURES THEREOF, HEATING THE RESULTANT LATEX-IMPREGNATED LAP AT A TEMPERATURE IN THE RANGE OF FROM ABOUT 60* TO ABOUT 80*C. FOR A TIME PERIOD REQUISITE TO COAGULATE SAID LATEX AND BIND THE FIBERS OF SAID LAP TOGETHER AND TO PRODUCE A BONDED LAP CONTAINING WATER IN AN AMOUNT APPRECIABLY ABOVE 50% BY WEIGHT OF SAID LATEX-IMPREGNATED LAP, THEREAFTER SQUEEZING SAID WATER-CONTAINING BONDED LAP TO REDUCE THE WATER CONTENT THEREOF TO A LEVEL IN THE RANGE OF FROM ABOUT 20 TO ABOUT 50% BY WEIGHT BASED ON THE DRY WIGHT OF THE LAP, AND THEN DRYING THE RESULTING BONDED LAP OF REDUCED WATER CONTENT AT A TEMPERATURE OF ABOUT 120*C. TO PROVIDE A POROUS, BONDED LAP HAVING FREE SPACES THREWITHIN CORRESPONDING ESSENTIALLY TO THOSE SPACES OCCUPIED BY SAID WATER PRESENT IN SAID BONDED LAP OF REDUCED WATER CONTENT PRELIMINARY TO SAID DRYING STEP.
US92170A 1953-12-17 1961-02-28 Process for making and finishing artificial hides or leathers Expired - Lifetime US3185582A (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
DENDAT1288061D DE1288061B (en) 1961-02-28
DEA21751A DE1204618B (en) 1953-12-17 1954-12-16 Process for treating the surface of artificial leather
FR1115866D FR1115866A (en) 1953-12-17 1954-12-16 Process for finishing artificial skins or leathers made essentially with natural or synthetic fibers agglomerated by a natural or synthetic latex
FR1115864D FR1115864A (en) 1953-12-17 1954-12-16 Process for obtaining the hardening of artificial skins or leathers
US92170A US3185582A (en) 1953-12-17 1961-02-28 Process for making and finishing artificial hides or leathers
FR888990A FR81199E (en) 1961-02-28 1962-02-23 Process for finishing artificial skins or leathers made essentially with natural or synthetic fibers agglomerated by a natural or synthetic latex
GB7777/62A GB992261A (en) 1961-02-28 1962-02-28 A process for making and finishing artificial hides or leathers
NL275386A NL126058C (en) 1961-02-28 1962-02-28
ES0275317A ES275317A1 (en) 1961-02-28 1962-02-28 Process for making and finishing artificial hides or leathers

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US92170A US3185582A (en) 1953-12-17 1961-02-28 Process for making and finishing artificial hides or leathers

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NL (1) NL126058C (en)

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US3356517A (en) * 1963-12-17 1967-12-05 Scott Paper Co Heat coagulatable paper coating composition
US3376158A (en) * 1966-03-16 1968-04-02 Du Pont Process for producing microporous polymeric structures by freeze-coagulation of latices
US3483016A (en) * 1966-08-02 1969-12-09 United Shoe Machinery Corp Treatment of collagen fiber sheet
US3494781A (en) * 1966-12-20 1970-02-10 Shell Oil Co Process for producing a leather substitute
US3519459A (en) * 1964-09-23 1970-07-07 Ciba Ltd Process for producing finely porous coatings
US3524792A (en) * 1966-11-07 1970-08-18 Robert T Dawes Elastically-stretchable,leather-like material and method of making the same
US3620797A (en) * 1969-01-14 1971-11-16 Dhj Ind Inc Impregnation of a nonwoven fabric
US3874913A (en) * 1972-05-12 1975-04-01 Peter Frederick Lofts Method for making a nonwoven fabric
US3920868A (en) * 1971-10-22 1975-11-18 Hoechst Ag Process for the manufacture of a chemically bonded non-woven fiber material in sheet form
US3958057A (en) * 1974-06-28 1976-05-18 Kuraray Co., Ltd. Leather-like sheet material having excellent pearl-like tint and process for preparation thereof
US20050044647A1 (en) * 2002-09-20 2005-03-03 Colgate-Palmolive Company Oral care implement
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US8151397B2 (en) 2002-08-09 2012-04-10 Colgate-Palmolive Company Oral care implement having flexibly supported cleaning elements extending in opposite directions
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DE1290115B (en) * 1963-01-10 1969-03-06 Pfeiffer Richard Process for the production of colored fleece artificial leather
DE2621195C2 (en) * 1976-05-13 1982-10-14 Giulini Chemie Gmbh, 6700 Ludwigshafen Stiffening materials for shoes and parts of shoes
NL8600359A (en) * 1986-02-13 1987-09-01 Polysar Financial Services Sa LATEX, PROCESS FOR THE MANUFACTURE OF A CONSOLIDATED FILES AND CONSOLIDATED FILES, MADE BY THE METHOD.
CN107937632B (en) * 2017-12-22 2020-01-17 德州兴隆皮革制品有限公司 Method for manufacturing sofa leather

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US2064360A (en) * 1934-07-25 1936-12-15 Brown Co Manufacture of smooth-faced webs of interfelted fiber
US2191654A (en) * 1938-08-10 1940-02-27 Du Pont Leather finish
US2446806A (en) * 1941-06-12 1948-08-10 Bernard Andre Production of substitute leather
US2686764A (en) * 1951-11-09 1954-08-17 Du Pont Leather-finishing compositions containing caprolactam and a resinous polymer
US2696447A (en) * 1952-05-13 1954-12-07 Armstrong Cork Co Felt base floor covering
US2731358A (en) * 1952-11-10 1956-01-17 Armstrong Cork Co Plastic floor coverings and method for producing same
US2742377A (en) * 1952-05-13 1956-04-17 Armstrong Cork Co Flexible floor covering and method of making the same
CA607607A (en) * 1960-10-25 C. Wetterau Paul Decorative surface coverings
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CA607607A (en) * 1960-10-25 C. Wetterau Paul Decorative surface coverings
US1905749A (en) * 1929-09-17 1933-04-25 Brown Co Manufacture of artificial leather
US2064360A (en) * 1934-07-25 1936-12-15 Brown Co Manufacture of smooth-faced webs of interfelted fiber
US2191654A (en) * 1938-08-10 1940-02-27 Du Pont Leather finish
US2446806A (en) * 1941-06-12 1948-08-10 Bernard Andre Production of substitute leather
US2686764A (en) * 1951-11-09 1954-08-17 Du Pont Leather-finishing compositions containing caprolactam and a resinous polymer
US2696447A (en) * 1952-05-13 1954-12-07 Armstrong Cork Co Felt base floor covering
US2742377A (en) * 1952-05-13 1956-04-17 Armstrong Cork Co Flexible floor covering and method of making the same
US2731358A (en) * 1952-11-10 1956-01-17 Armstrong Cork Co Plastic floor coverings and method for producing same
US3039913A (en) * 1959-05-04 1962-06-19 Little Inc A Reinforced resin sheet

Cited By (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3356517A (en) * 1963-12-17 1967-12-05 Scott Paper Co Heat coagulatable paper coating composition
US3519459A (en) * 1964-09-23 1970-07-07 Ciba Ltd Process for producing finely porous coatings
US3376158A (en) * 1966-03-16 1968-04-02 Du Pont Process for producing microporous polymeric structures by freeze-coagulation of latices
US3483016A (en) * 1966-08-02 1969-12-09 United Shoe Machinery Corp Treatment of collagen fiber sheet
US3524792A (en) * 1966-11-07 1970-08-18 Robert T Dawes Elastically-stretchable,leather-like material and method of making the same
US3494781A (en) * 1966-12-20 1970-02-10 Shell Oil Co Process for producing a leather substitute
US3620797A (en) * 1969-01-14 1971-11-16 Dhj Ind Inc Impregnation of a nonwoven fabric
US3920868A (en) * 1971-10-22 1975-11-18 Hoechst Ag Process for the manufacture of a chemically bonded non-woven fiber material in sheet form
US3874913A (en) * 1972-05-12 1975-04-01 Peter Frederick Lofts Method for making a nonwoven fabric
US3958057A (en) * 1974-06-28 1976-05-18 Kuraray Co., Ltd. Leather-like sheet material having excellent pearl-like tint and process for preparation thereof
US7845042B2 (en) 2002-08-09 2010-12-07 Colgate-Palmolive Company Oral care implement
US8990996B2 (en) 2002-08-09 2015-03-31 Colgate-Palmolive Company Toothbrush
US10512323B2 (en) 2002-08-09 2019-12-24 Colgate-Palmolive Company Oral care implement
US9603441B2 (en) 2002-08-09 2017-03-28 Colgate-Palmolive Company Toothbrush
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US7047591B2 (en) 2002-09-20 2006-05-23 Colgate-Palmolive Company Oral care implement
US20050044647A1 (en) * 2002-09-20 2005-03-03 Colgate-Palmolive Company Oral care implement
US7458125B2 (en) 2002-09-20 2008-12-02 Colgate-Palmolive Company Oral care implement
US20070119010A1 (en) * 2002-09-20 2007-05-31 Hohlbein Douglas J Oral care implement
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Also Published As

Publication number Publication date
DE1204618B (en) 1965-11-11
FR81199E (en) 1963-08-09
DE1288061B (en) 1969-01-30
FR1115864A (en) 1956-04-30
NL126058C (en) 1968-10-15
FR1115866A (en) 1956-04-30
ES275317A1 (en) 1962-07-16
GB992261A (en) 1965-05-19

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