US3326713A - Breathable and waterproof coated fabric and process of making same - Google Patents

Breathable and waterproof coated fabric and process of making same Download PDF

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US3326713A
US3326713A US340893A US34089364A US3326713A US 3326713 A US3326713 A US 3326713A US 340893 A US340893 A US 340893A US 34089364 A US34089364 A US 34089364A US 3326713 A US3326713 A US 3326713A
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fabric
coating
elastomer
fluorochemical
breathable
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Vernon C Smith
Jr Everett H Hinton
Delbert A Davis
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Burlington Industries Inc
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Burlington Industries Inc
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    • 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
    • D06N3/0059Organic ingredients with special effects, e.g. oil- or water-repellent, antimicrobial, flame-resistant, magnetic, bactericidal, odour-influencing agents; perfumes
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/20Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
    • Y10T442/2041Two or more non-extruded coatings or impregnations
    • Y10T442/2098At least two coatings or impregnations of different chemical composition
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/20Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
    • Y10T442/2221Coating or impregnation is specified as water proof
    • Y10T442/2238Fluorocarbon containing

Definitions

  • the present invention relates to coated fabric, e.g. rainwear or the like. More particularly, the invention is concerned with a coated fabric of the type indicated which is breathable and waterproof yet retains the desirable hand and appearance of an uncoated product.
  • the principal object of the present invention is to obviate prior art difliculties and provide a coated fabric, suitable for use as rainwear or the like, which is breathable and waterproof and also demonstrates a highly desirable textile hand.
  • a more specific object of the invention is to provide a coated fabric of the type indicated which has the appearance and hand of an uncoated product.
  • Another object is to provide a process for preparing the ihdicated fabric.
  • FIGURE 1 is an enlarged vertical sectional view of a fabric processed according to the invention.
  • FIGURE 2 is a corresponding view of a similar product without the pretreatment of the invention.
  • the objects of the invention are realized by pretreating the fabric with a fiuorochemical compound having oil repellent properties and then coating the fabric with any conventional type of waterproofing resin or elastomer composition.
  • the fiuorochemical compound is applied to the fabric in the form of a dispersion or solution in water or organic liquid.
  • the thus treated fabric is dried and cured and the waterproofing composition is then applied in an appropriate vehicle, e.g. an organic solvent, followed again by drying and curing.
  • an appropriate vehicle e.g. an organic solvent
  • a fluorochemi cal may be applied to nylon or cotton fabric after which the fabric is dried and cured.
  • a polyurethane coating or the equivalent may then be applied to the fabric.
  • the polyurethane coating on the fiuorochemical pretreated product seems to ride on the surface of the fabric without significant penetration into the fabric due apparently to the action of the fiuorochemical compound.
  • any of the conventional fiuorochemical compounds which have oil repellent properties can be used herein.
  • acrylates and methacrylates of hydroxyl compounds containing a highly fluorinated residue and their polymers and copolymers can be used.
  • Fluorochemical compounds of this type are defined with greater particularity in U.S. Patents 2,642,416; 2,826,564; 2,839,513;
  • fiuorochemical compounds which can be employed include the chromium coordination complexes of saturated perfluoromonocarboxylic acids of which the chromium complexes of perfluorobutyric acid and perfiuorooctanoic acid are representative.
  • Fluorochemical compounds suitable for use herein are available commercially, for example, those marketed under the tradename Scotchgard 1 such as Scotchgard PC 205 and PC 208 and Zepel. Of these compounds, the Scotchgard PC 205 and FC 208 products, which are available in emulsion form, may be described according to U.S. Patent 2,803,615 by the following general formula:
  • R1 II in which X is a value between 3 and 13 inclusive, R is lower alkyl, such as methyl, ethyl, propyl, and the like, having 1-6 atoms, R is alkylene containing 1-12 carbon atoms and R is H, methyl or ethyl.
  • the product Zepel is also available in emulsion form and while it is chemically different from the Scotchgard products, it is a fluorochemical oil repellent containing fluorocarbon tails composed of CF groups which may end in a terminal CF group.
  • fiuorochemical compounds of the type indicated are known to demonstrate a water repellent effect but they are not considered to be waterproofing materials. Nevertheless, in the present case, the fluorocarbon pretreatment followed by the treatment with a waterproofing material gives a waterproofing effect superior to that obtained when the pretreatment is omitted. This is highly unusual and points up the unexpected nature of the invention.
  • the fiuorochemical compound may be applied to the fabric by padding the latter with an aqueous or organic system containing the pretreating compound.
  • aqueous emulsions or like compositions containing from 0.5% to 5% by weight fiuorochemical compound as supplied or compounds are used with from 0.01 to 1.0% of the compound or mixture of such compounds being deposited on the fabric, based on the weight of dry fabric.
  • the conditions which are used to dry and cure the fabric after application of the fiuorochemical compound will vary depending on the fluorocarbon and liquid medium utilized as well as the fabric undergoing treatment. However, a temperature in the range of 300 to 375 F. for 1 to 5 minutes will usually be sufficient for this purpose.
  • the waterproofing composition there may be used any known water-insoluble film-forming, curable resin or polymer.
  • Silastic or silicone elastomer coatings are preferred but other materials, e.g. acrylics, vinyls, polyurethanes and the like may be used.
  • a typical silastic for use herein is that commercially available as Dow XT- 40025 or Dow XT-40057 (30% solids as received, prod- Registered trademark of Minnesota Mining and Manufacturing Company (also known as 3M 2 Registered trademark of E. I. Du Pont.
  • x has an average value from 1.9 to 2, inclusive.
  • the waterproofing resin will generally be applied from a solution, dispersion or emulsion thereof in an inert organic liquid which does not affect the fabric or the fiuorochemical compound.
  • a preferred solvent is Varsol (a product of the Standard Oil Company), although other vehicles which may be used include xylene, toluene, heptane, trichloroethylene, perchloroethylene or any other solvent which is compatible with the elastomer being used.
  • the amount of waterproofing resin applied to the fabric will vary but, generally speaking, this will be in the area of 0.1 oz. to 2.0 oz. per square yard additional weight added to the fabric.
  • Knife coating or other appropriate means may be used and the fabric may be so coated on what is to be its front side or back side only or both sides. Desirably, care is taken to insure that all, or substantially all, of the resin is just below the fabric surface so as to minimize the possibility of a rubbery or Waxy feel and assure adhesion. At the same time, however, care must be taken not to press or force the material down too far into the fabric since this might have an undesirable effect on the hand.
  • the conditions used to dry and cure the fabric after the application of the film-forming resin composition will also vary considerably depending on such conditions as the fabric structure and composition, the nature of the resins used, etc. Usually, however, the temperature of drying is in the range 200300 F. for 1-10 minutes followed by curing at 250 -375 for 1-10 minutes. The temperature of the cure is limited only by the heat properties of the fiber in the fabric.
  • catalysts may be used in both the fluorochemical pretreatment and the subsequent resin or elastomer application. Additionally, it will be recognized that the invention is applicable broadly to any and all fabrics comprising natural and/or synthetic fibers, e.g. cotton, rayon, glass, nylon, polyester (polyethylene terephthalate), acrylics, etc.
  • Example A A 100% cotton rainwear fabric was padded with 3% Scotchgard 205 and 1% Rhotex A-9, dried and cured two minutes at 350 F. to obtain an oil rating of 110.
  • This Scotchgard treated fabric (specimen 1 below) was then knife coated with a mixture of 66% Dow XT40025 (or Dow 23), 0.5% QZ-80925, 1.8% Catalyst 23A, 0.5% HAc and 31.2% Varsol 3.
  • a control sample (specimen 2) without Scotchgard was knife coated with the same silastic elastomer mixture. Both fabrics were knife coated two times on the back of the fabric. The results obtained were:
  • the beneficial effect of the fiuorochemical pretreatment is readily apparent from the above example.
  • the hydrostatic head rating of the silastic rubber coated fabric is increased from 35 cm. for no pretreatment to 110 cm. with the pretreatment.
  • Hydrostatic head is the best measure of the waterproofness of a fabric or film and the rating of 110 cm., for the pretreated specimen 1 indicates that the product is essentially waterproof, yet it retains a good amount of breathability or water vapor transmission.
  • the silastic elastomer is durable to laundering and dry cleaning, at least a major proportion of the silastic properties being retained through five commercial dry cleanings or even more.
  • the product obtained using the fiuorochemical pretreatment product was much softer and there was no evidence of silastic elastomer strikethrough whereas the silastic elastomer coated fabric obtained without the pretreatment was stiff and showed evidence of severe strikethrough to the face of the fabric.
  • the product prepared according to the invention (specimen 1 above)
  • no plastic or rubber film was evident on the fabric surface, the fabric retaining its textile appearance and feel. This is an extremely important advantage over prior waterproofing procedures where the rubber or plastic film is evident to the touch and gives the product a clammy or otherwise undesirable feel.
  • Example B Results-Hydrostatic Head Specimens Amount Fluoro- 3-M Oil Elastomer carbon in pretreat Rating Formulation Original After 5 Dry Cleanings 0 0 None 0 0 i 0 0 20% in Varsol- 33 10 Scotchgard 205-. 0 do 34 10 lg? gcogclrilgarg 30g.” do 36 10 co 0 gar 0 ⁇ 1% Rhotex A-9- i 100 48 15 ZePeL" 100+ -do 45 1s 3% Scotchgard -.90 NoneControl 37 (Commercial fin.).
  • this material or its equivalent may be advantageously used in conjunction with the fluorochemical materials as a water repellent extender or to otherwise enhance the properties of the fluorochemical for present purposes.
  • the fluorochemical serves to provide a water repellent face.
  • the fluorochemical will be a satisfactory water repellent without an extender such as Zelan, Phobotex, etc., but with addition of the proper amount of these extenders, a superior Water repellent face can be obtained.
  • the amount of Zelan which may be used for such purposes should be sufficiently low to give an oil rating of about 90 or above. More than this amount of Zelan, e.g. the 8% used in the example, has an undesirable effect on the hydrostatic head after the silicone elastomer is applied.
  • Example F Approximately 100 yards each of the following fabric were processed full width on commercial coating equipment:
  • ScotchgartL- 100 2 coats backside 115 42 17 0 0 do 33 .47 18 2.5% Scotchgard 100 1 coat each side- 74 69 19 0 o 34 .59 20 2.5% Seotchgaid" 100 2 coats backside... 150+ .59 21 0 0 ..do 36 .49
  • the fabric in this case was -l00% cotton raincoat fabric.
  • a mixture of 20% solids Dow XT40025 with Varsol was knife coated in all cases using a process as outlined in Example A above.
  • Specimens 20 and 21 dilfer from specimens 16 and 17 in that an attempt was made to apply a heavier knife coating to specimens 20 and 21.
  • the results show that a heavier coating was applied and it will be noted that despite the weight of the coating, the hydrostatic head of the non-pretreated fabric did not improve beyond 36 cm.
  • the pre pared fabric was padded with a bath containing on the weight of the bath.
  • the padded fabric was dried and cured simultaneously at 350 at 15 y.p.m.
  • the treated fabric was then knife coated on the back side with a formulation as follows:
  • Catalyst 23A (Dow Corning) is a product used as the 3-M Elastomer Temp. 7 Original Specimens Oil Coating Drying, Fiber Fabric Color Hydrostatic Rating Weight, F. Content Description Head, Avg.
  • this particular gray raincoat fabric was thicker and heavier than the olive. Both fabrics passed under the knife at the same knife setting. The gray fabric being thicker received a thinner coat of silicone elastomer as evidenced by the elastorner coating weight. It will be noted that although the coating weight of 0.3 oz./sq. yd. was half that of the other samples, the gray raincoat fabric performed equally as well as a comparable fabric with a heavier coating.
  • the fabric was passed through a mixture of silicone elastotrier/solvent as in Example A and the excess squeezed out by running through a nip roll.
  • the padded fabric was then run continuously into a tenter frame for drying and curing. While the amount of silicone elastomer deposited from the dilute solution used did not make large changes in the hydrostatic head, in each case the presence of the fluorochemical increased the hydrostatic head significantly.
  • Zelan is a pyridinium acid chloride derivative of stearamide. It is available as a pre-emulsified solid which forms a stable emulsion on stirring in hot water.
  • the following structure is typical of compounds of this type.
  • Rhotex A-9 is a product supplied by Rohm & Haas Company as a water dispersible emulsion of Phobotex is a tradename for Cibas water repellent product called a triazine fatty water repellent and is a WATER RESISTANCE RAIN TESTSTANDARD TEST METHOD AATCC 35-1961 Shower Rain Storm Height of Column 2 ft 2 ft 3 ft. Time of Exposure 30 seconds... 2 min 5 min Test fails if more than 1 gram penetrates (ASA Ir-22 standards #10.27-1960).
  • the fabric is first coated with a definite thickness of elastomer which may be vinyl, rubber or the like.
  • the coating even if colored to match the fabric color is nevertheless visible and has the feel of conventional rubber coated raincoat.
  • the coating is filled with starch and this starch is subsequently expanded by heat and then removed with acids or enzymes so as to leave many microporous interconnecting holes through the thickness of the fabric.
  • This leaching technique makes the film breathable, or at least allows the passage of water vapor through the film.
  • Another prior technique utilizes salt which is then leached out to leave mi-croporous holes.
  • the steps in this alternate process involve (a) grinding together the elastomer, color, salt and any other ingredient; (b) knife coat the resulting elastomer composition; (c) dry and cure; (d) leach out the salt (or starch if the latter is used); (e) dry; and (f) apply water repellent to the uncoated surface.
  • the present process eliminates the leaching operation and gives the desirable characteristics noted above by the controlled coating of the elastomer which results from the preliminary application of the fiuorochemical compound.
  • the natural voids formed by the interstices of the fabric and by means of the controlled coating fill these voids until submicroscopic voids are achieved. It is believed that without the fluorochemical treatment, the elastomer utilized will not fill up the natural voids present in fabric. Rather, the solvent or liquid vehicle penetrates into the accessible regions between the fibers and around the yarn bundle, since from visual observation, there is very little change in the size of the natural voids before or after coating the elastomer.
  • the fluorochemical or fluorocarbon pretreatment does not permit the solvent to penetrate into the accessible region between the fibers and around the yarn bundle. Accordingly, the solvent/elastomer system coated on the fabric must remain at or near the surface. The only accessible region for the elastomer is the fiber bundle near the surface and the natural voids are filled to give the submicroscopic voids which give breathability while retaining the desired waterproofness and hand.
  • FIGURE 1 shows the fabric 2 with one surface (e.g. the outer face) coated with a fluorocarbon barrier layer 4.
  • the opposite surface of the fabric carries a similar fluorocarbon barrier layer 6 with the waterproofing elastomer coating 8 thereover.
  • FIG- URE 2 illustrates the case where no fluorocarbon pretreatment is used. In this situation, the entire fabric 10 is deeply penetrated and more or less saturated with elastomer as shown by the shading resulting in a product having poor hand.
  • a coated fabric suitable for rainwear which is breathable and waterproof and 'having substantially the appearance and hand of an uncoated fabric, which comprises a fabric, a first coating on said fabric of a fluorochemical having an oil rating of at least 70, a second coating thereon of a waterproof curable polymer, said first fluorochemical coating being at least partially disposed within the interstices of the fabric whereby the said second waterproof coating is prevented from substantially penetrating the said interstices and whereby said second coating lies substantially at or near the surface of the fabric.
  • a process for producing a textile fabric suitable for rainwear which is breathable and waterproof and having substantially the appearance and hand of an uncoated fabric comprising depositing at least partially within the interstices of the fabric a fluorochemical having an oil rating of at least about 70, curing the fluorochemical, applying to the fabric a curable waterproofing polymer composition and curing said polymer composition, whereby the cured fluorochemical prevents substantion penetration of the uncured polymer into the interstices of the fabric.
  • composition is an elastomer in liquid vehicle, said composition being applied by knife coating.
  • composition is an elastomer in a liquid vehicle, said composition being applied by padding.

Description

June 20, 1967 V.* c. SMITH ET AL 3,326,713
BREATHABLE AND WATERPROOF COATED FABRIC AND PROCESS OF MAKING SAME Filed Jan. 29, 1964 INVENTOR3 Vii/VOA 6'. 31w 1w [Fl/17577 M ////yrang JR J54 es/rrfl .Daw:
ATTORNEYS United States Patent 0 3,326,713 BREATHABLE AND WATERPROOF COATED FABRIC AND PROCESS OF MAKING SAME Vernon C. Smith and Everett H. Hinton, Jr., Greensboro, and Delbert A. Davis, Kernersville, N.C., assignors to Burlington Industries, Inc., Greensboro, N.C., a cor= poration of Delaware Filed Jan. 29, 1964, Ser. No. 340,893
8 Claims. (Cl. 117-76) The present invention relates to coated fabric, e.g. rainwear or the like. More particularly, the invention is concerned with a coated fabric of the type indicated which is breathable and waterproof yet retains the desirable hand and appearance of an uncoated product.
Extensive prior efforts have been made to obtain rainwear fabrics which are not only waterproof and breathable, but also possess a soft and otherwise desirable hand. Despite these efforts, however, no completely satisfactory product has previously been developed. Thus, for example, while it is possible to prepare fabrics having desirable degrees of breathability and waterproofing using specialized and costly coating techniques or treatments, the resulting products usually demonstrate an unattractive hand. In particular, the coating may make the fabric stiff or boardy and even with a thin and soft type of coating, the product generally has an undesirable rubbery or waxy feel.
Obviously, it is not an easy thing to obtain an optimum combination of the desired characteristics since breathability and waterproofing, for example, are at least to some extent opposed to each other. Essentially the same is true in the case of hand since almost any coating material which is used in normal manner to waterproof a fabric will have some undesirable effect on the hand.
The principal object of the present invention is to obviate prior art difliculties and provide a coated fabric, suitable for use as rainwear or the like, which is breathable and waterproof and also demonstrates a highly desirable textile hand. A more specific object of the invention is to provide a coated fabric of the type indicated which has the appearance and hand of an uncoated product. Another object is to provide a process for preparing the ihdicated fabric. Other objects will alsobe apparent from the following detailed description of the invention and the accompanying drawings wherein:
FIGURE 1 is an enlarged vertical sectional view of a fabric processed according to the invention; and
FIGURE 2 is a corresponding view of a similar product without the pretreatment of the invention.
Broadly stated, the objects of the invention are realized by pretreating the fabric with a fiuorochemical compound having oil repellent properties and then coating the fabric with any conventional type of waterproofing resin or elastomer composition. Advantageously, the fiuorochemical compound is applied to the fabric in the form of a dispersion or solution in water or organic liquid. The thus treated fabric is dried and cured and the waterproofing composition is then applied in an appropriate vehicle, e.g. an organic solvent, followed again by drying and curing. Without intending to be limited to any particular theory, it appears that the fluorocarbon prevents the solvent or liquid vehicle used for applying the Waterproofing material from soaking into the fabric and carrying the clastomer or equivalent into the interstices of the fabric where breathability and hand might be detrimentally affected.
As a typical illustration of the invention, a fluorochemi cal may be applied to nylon or cotton fabric after which the fabric is dried and cured. A polyurethane coating or the equivalent may then be applied to the fabric. A comparison of this fabric with the corresponding product where the fiuorochemical pretreatment is omitted, shows that the dual treated fabric has a much softer hand and is otherwise more attractive. The polyurethane coating on the fiuorochemical pretreated product seems to ride on the surface of the fabric without significant penetration into the fabric due apparently to the action of the fiuorochemical compound.
Any of the conventional fiuorochemical compounds which have oil repellent properties can be used herein. For example, acrylates and methacrylates of hydroxyl compounds containing a highly fluorinated residue and their polymers and copolymers can be used. Fluorochemical compounds of this type are defined with greater particularity in U.S. Patents 2,642,416; 2,826,564; 2,839,513;
2,803,615. Other fiuorochemical compounds which can be employed include the chromium coordination complexes of saturated perfluoromonocarboxylic acids of which the chromium complexes of perfluorobutyric acid and perfiuorooctanoic acid are representative. Fluorochemical compounds suitable for use herein are available commercially, for example, those marketed under the tradename Scotchgard 1 such as Scotchgard PC 205 and PC 208 and Zepel. Of these compounds, the Scotchgard PC 205 and FC 208 products, which are available in emulsion form, may be described according to U.S. Patent 2,803,615 by the following general formula:
R3 F G-(OFz)x-SO2NR OC0=CH;
R1 II in which X is a value between 3 and 13 inclusive, R is lower alkyl, such as methyl, ethyl, propyl, and the like, having 1-6 atoms, R is alkylene containing 1-12 carbon atoms and R is H, methyl or ethyl. The product Zepel is also available in emulsion form and while it is chemically different from the Scotchgard products, it is a fluorochemical oil repellent containing fluorocarbon tails composed of CF groups which may end in a terminal CF group.
Generally speaking, fiuorochemical compounds of the type indicated (e.g. Scotchgard) are known to demonstrate a water repellent effect but they are not considered to be waterproofing materials. Nevertheless, in the present case, the fluorocarbon pretreatment followed by the treatment with a waterproofing material gives a waterproofing effect superior to that obtained when the pretreatment is omitted. This is highly unusual and points up the unexpected nature of the invention.
As noted, the fiuorochemical compound may be applied to the fabric by padding the latter with an aqueous or organic system containing the pretreating compound. Usually, aqueous emulsions or like compositions containing from 0.5% to 5% by weight fiuorochemical compound as supplied or compounds are used with from 0.01 to 1.0% of the compound or mixture of such compounds being deposited on the fabric, based on the weight of dry fabric.
The conditions which are used to dry and cure the fabric after application of the fiuorochemical compound will vary depending on the fluorocarbon and liquid medium utilized as well as the fabric undergoing treatment. However, a temperature in the range of 300 to 375 F. for 1 to 5 minutes will usually be sufficient for this purpose.
As the waterproofing composition, there may be used any known water-insoluble film-forming, curable resin or polymer. Silastic or silicone elastomer coatings are preferred but other materials, e.g. acrylics, vinyls, polyurethanes and the like may be used. A typical silastic for use herein is that commercially available as Dow XT- 40025 or Dow XT-40057 (30% solids as received, prod- Registered trademark of Minnesota Mining and Manufacturing Company (also known as 3M 2 Registered trademark of E. I. Du Pont.
uct of Dow Corning Corp). This and other suitable silastic of siloxane elastomers are described in US. Patent 3,076,726 and may be represented by the formula:
wherein x has an average value from 1.9 to 2, inclusive.
The waterproofing resin will generally be applied from a solution, dispersion or emulsion thereof in an inert organic liquid which does not affect the fabric or the fiuorochemical compound. A preferred solvent is Varsol (a product of the Standard Oil Company), although other vehicles which may be used include xylene, toluene, heptane, trichloroethylene, perchloroethylene or any other solvent which is compatible with the elastomer being used.
The amount of waterproofing resin applied to the fabric will vary but, generally speaking, this will be in the area of 0.1 oz. to 2.0 oz. per square yard additional weight added to the fabric. Knife coating or other appropriate means may be used and the fabric may be so coated on what is to be its front side or back side only or both sides. Desirably, care is taken to insure that all, or substantially all, of the resin is just below the fabric surface so as to minimize the possibility of a rubbery or Waxy feel and assure adhesion. At the same time, however, care must be taken not to press or force the material down too far into the fabric since this might have an undesirable effect on the hand.
The conditions used to dry and cure the fabric after the application of the film-forming resin composition will also vary considerably depending on such conditions as the fabric structure and composition, the nature of the resins used, etc. Usually, however, the temperature of drying is in the range 200300 F. for 1-10 minutes followed by curing at 250 -375 for 1-10 minutes. The temperature of the cure is limited only by the heat properties of the fiber in the fabric.
Conventional catalysts may be used in both the fluorochemical pretreatment and the subsequent resin or elastomer application. Additionally, it will be recognized that the invention is applicable broadly to any and all fabrics comprising natural and/or synthetic fibers, e.g. cotton, rayon, glass, nylon, polyester (polyethylene terephthalate), acrylics, etc.
The invention is illustrated, but not limited, by the following examples wherein parts are by weight unless otherwise stated:
Example A A 100% cotton rainwear fabric was padded with 3% Scotchgard 205 and 1% Rhotex A-9, dried and cured two minutes at 350 F. to obtain an oil rating of 110. This Scotchgard treated fabric (specimen 1 below) was then knife coated with a mixture of 66% Dow XT40025 (or Dow 23), 0.5% QZ-80925, 1.8% Catalyst 23A, 0.5% HAc and 31.2% Varsol 3. At the same time, a control sample (specimen 2) without Scotchgard was knife coated with the same silastic elastomer mixture. Both fabrics were knife coated two times on the back of the fabric. The results obtained were:
The beneficial effect of the fiuorochemical pretreatment is readily apparent from the above example. Thus, the hydrostatic head rating of the silastic rubber coated fabric is increased from 35 cm. for no pretreatment to 110 cm. with the pretreatment. Hydrostatic head is the best measure of the waterproofness of a fabric or film and the rating of 110 cm., for the pretreated specimen 1 indicates that the product is essentially waterproof, yet it retains a good amount of breathability or water vapor transmission. It was also found that the silastic elastomer is durable to laundering and dry cleaning, at least a major proportion of the silastic properties being retained through five commercial dry cleanings or even more. Furthermore, the product obtained using the fiuorochemical pretreatment product was much softer and there was no evidence of silastic elastomer strikethrough whereas the silastic elastomer coated fabric obtained without the pretreatment was stiff and showed evidence of severe strikethrough to the face of the fabric. Additionally, with the product prepared according to the invention (specimen 1 above), no plastic or rubber film was evident on the fabric surface, the fabric retaining its textile appearance and feel. This is an extremely important advantage over prior waterproofing procedures where the rubber or plastic film is evident to the touch and gives the product a clammy or otherwise undesirable feel.
5 The following results were obtained on testing speci- Water Resistance Test Storm (3 it. head, 5 min),
Spray Rating Grams Water Passing Specimens Through Fabric Original After 5 Dry Original After 5 Dry Cleanings Cleanings The dry cleaning durability of the finish applied to the fabric according to the present invention is readily apparent from the foregoing.
,. It is important to the success of the invention that the fiuorochemical pretreatment have the proper oil rating. This is shown by the following example wherein the standard 3-M oil rating technique is used for evaluation purposes:
Example B Results-Hydrostatic Head Specimens Amount Fluoro- 3-M Oil Elastomer carbon in pretreat Rating Formulation Original After 5 Dry Cleanings 0 0 None 0 0 i 0 0 20% in Varsol- 33 10 Scotchgard 205-. 0 do 34 10 lg? gcogclrilgarg 30g." do 36 10 co 0 gar 0 {1% Rhotex A-9- i 100 48 15 ZePeL" 100+ -do 45 1s 3% Scotchgard -.90 NoneControl 37 (Commercial fin.).
From the above data, the importance of a proper oil rating before application of the solvent/elastomer can be seen. Although the amount of elastomer applied to the fabrics was less than optimum, all samples were prepared under exactly the same conditions. It will be seen that, as the oil rating increases, the hydrostatic head increases. A minimum oil rating of at least about 70 is necessary for present purposes, the beneficial and unexpected action of the fluorochemical not occurring at significantly lower oil ratings.
Example ,C
This example illustrates the use of the present process with various types of fabrics using the process of Example A except for the indicated pretreatment:
In the above, the hydrostatic test results clearly indicate the benefit of the fluorochemical pretreatment. Regardless of fiber content, the pretreatment with fluorocarbon always results in a higher hydrostatic head rating.
6 The harmful efiect of using too much Zelan, an oleophilic water repellent commercially available from Du Pont, in the fluorochemical pretreatment bath is shown by the above.
While this example shows the undesirable effects of using a relatively large amount of Zelan, it will be appreciated that this material or its equivalent may be advantageously used in conjunction with the fluorochemical materials as a water repellent extender or to otherwise enhance the properties of the fluorochemical for present purposes. For instance, if the elastomer is coated on the back side only, then the fluorochemical serves to provide a water repellent face. The fluorochemical will be a satisfactory water repellent without an extender such as Zelan, Phobotex, etc., but with addition of the proper amount of these extenders, a superior Water repellent face can be obtained. The amount of Zelan which may be used for such purposes should be sufficiently low to give an oil rating of about 90 or above. More than this amount of Zelan, e.g. the 8% used in the example, has an undesirable effect on the hydrostatic head after the silicone elastomer is applied.
Example F Approximately 100 yards each of the following fabric were processed full width on commercial coating equipment:
All of the above fabrics were knife coated two coats on OL/yd; the back side of the fabric with 20%lsollids mixture of ten fabric 42 Dow XT-40025 Elastomer and Varso so vent. Olive cotton raincoating 67 Example D Gray cotton raincoating 7.2 This example illustrates the results obtained by varia- D /C tt n poplin 5.4 tion in the knife coating applications of the elastomer: Cotton sheeting 3.78
Pretreatment Added Speci- Amount Oil Knife Coating Hydrostatic weight of men Fluorocarbon Rating Variation Head Coating,
oz./sq. yd.
16 2.5% ScotchgartL- 100 2 coats backside 115 42 17 0 0 do 33 .47 18 2.5% Scotchgard 100 1 coat each side- 74 69 19 0 o 34 .59 20 2.5% Seotchgaid" 100 2 coats backside... 150+ .59 21 0 0 ..do 36 .49
The fabric in this case was -l00% cotton raincoat fabric. A mixture of 20% solids Dow XT40025 with Varsol was knife coated in all cases using a process as outlined in Example A above.
Specimens 20 and 21 dilfer from specimens 16 and 17 in that an attempt was made to apply a heavier knife coating to specimens 20 and 21. The results show that a heavier coating was applied and it will be noted that despite the weight of the coating, the hydrostatic head of the non-pretreated fabric did not improve beyond 36 cm.
After suitable scouring to obtain clean fabric, the pre pared fabric was padded with a bath containing on the weight of the bath. The padded fabric was dried and cured simultaneously at 350 at 15 y.p.m. The treated fabric was then knife coated on the back side with a formulation as follows:
whereas the hydrostatic head for the pretreated fabric Percent increased substantially.E l E DOW XTAOOQS n 660 e Catalyst 23-A 1,8 The importance of having the appropriate Oll rating 0925 binder 05 for the fluorochemical treatment is further shown by this Varso] 3 Solvent 3 1'2 example using the process of Example A except for the HAc 5 changes indicated:
El t Added Specimen Pretreatment 551%, Type Coating Hydrostatic Coating Percent Head, cm. Weight, Formula Oil Rating ozJsq. yd.
22 2% swmhgard-w 20 zoom each side... .85
h d... 23 o 20 .-..do 38 1.12
8% Zelan 7 Fabrics were dried at the temperature shown below at 30 y.p.m. The following results were obtained after curing at 375 F. at 10 y.p.m.:
mixture of various fatty oils and alcohols attached in some manner to a methylolmelamine nucleus.
Catalyst 23A (Dow Corning) is a product used as the 3-M Elastomer Temp. 7 Original Specimens Oil Coating Drying, Fiber Fabric Color Hydrostatic Rating Weight, F. Content Description Head, Avg.
Avg.
24 100 0.68 200 100% cotton. Rainwear- 150+ 25 100 *0. 29 200 ...do 150+ 26 100 0. 67 240 Dacron/cotton d 83 27 100 1. 34 240 100% Nylon- W hite 150+ 28 100 0.96 200 100% cotton..... Sheeting-. Bleached..- 85
*Note, this particular gray raincoat fabric was thicker and heavier than the olive. Both fabrics passed under the knife at the same knife setting. The gray fabric being thicker received a thinner coat of silicone elastomer as evidenced by the elastorner coating weight. It will be noted that although the coating weight of 0.3 oz./sq. yd. was half that of the other samples, the gray raincoat fabric performed equally as well as a comparable fabric with a heavier coating.
The fabrics so produced were further tested for other catalyst for Dow XT40025; while QZ80925 (also Dow repellent properties described below: Corning) is a binder and crosslinker for the Dow Original After 5 dry cleanings Specimens Spray Storm Water Vapor Spray Storm Water Vapor Face Test Transmission, Face Test Transgms/sq m./24 mission hrs.
Example G XT-40025.
This example illustrates a modification of the present process wherein the silicone elastomer is appled by padding rather than by knife coating as in the other examples:
After the fluorocarbon pretreatment, when used, the fabric was passed through a mixture of silicone elastotrier/solvent as in Example A and the excess squeezed out by running through a nip roll. The padded fabric was then run continuously into a tenter frame for drying and curing. While the amount of silicone elastomer deposited from the dilute solution used did not make large changes in the hydrostatic head, in each case the presence of the fluorochemical increased the hydrostatic head significantly.
It is to be noted, with respect to the various products referred to by tradename in the above examples and not hitherto otherwise identified, that Zelan is a pyridinium acid chloride derivative of stearamide. It is available as a pre-emulsified solid which forms a stable emulsion on stirring in hot water. The following structure is typical of compounds of this type.
Rhotex A-9 is a product supplied by Rohm & Haas Company as a water dispersible emulsion of Phobotex is a tradename for Cibas water repellent product called a triazine fatty water repellent and is a WATER RESISTANCE RAIN TESTSTANDARD TEST METHOD AATCC 35-1961 Shower Rain Storm Height of Column 2 ft 2 ft 3 ft. Time of Exposure 30 seconds... 2 min 5 min Test fails if more than 1 gram penetrates (ASA Ir-22 standards #10.27-1960).
SPRAY RATINGAATCC standard test method 22-1961.
01L RATINcMinnesota Mining and Manufacturing oil reiiglltiigr test 3M Technical Bulletin, appendix A, dated June gigriir vArort TaANsMrssIoNStandard test method ASTM A modified test where a sample of fabric for testing is securely and tightly mounted over a dish containing water. Sample and dish placed in a test chamber where air is circulated at a rate not less than 500 feet/minute.
Results reported as grams (water vapor transmitted) per sq. meter (of fabric area) per 24 hours (grams/sq. meter/24 hours).
On the basis of the foregoing description, the advantages of the present invention over prior techniques will be apparent to those skilled in the art. For example, in one existing prior procedure which is used on a commercial basis, the fabric is first coated with a definite thickness of elastomer which may be vinyl, rubber or the like. The coating, even if colored to match the fabric color is nevertheless visible and has the feel of conventional rubber coated raincoat. In said prior process, the coating is filled with starch and this starch is subsequently expanded by heat and then removed with acids or enzymes so as to leave many microporous interconnecting holes through the thickness of the fabric. This leaching technique makes the film breathable, or at least allows the passage of water vapor through the film. However, it will be recognized that such an operation is much more complicated than that contemplated herein. Another prior technique utilizes salt which is then leached out to leave mi-croporous holes. The steps in this alternate process involve (a) grinding together the elastomer, color, salt and any other ingredient; (b) knife coat the resulting elastomer composition; (c) dry and cure; (d) leach out the salt (or starch if the latter is used); (e) dry; and (f) apply water repellent to the uncoated surface. In contrast, the present process eliminates the leaching operation and gives the desirable characteristics noted above by the controlled coating of the elastomer which results from the preliminary application of the fiuorochemical compound. With the present method, the natural voids formed by the interstices of the fabric and by means of the controlled coating fill these voids until submicroscopic voids are achieved. It is believed that without the fluorochemical treatment, the elastomer utilized will not fill up the natural voids present in fabric. Rather, the solvent or liquid vehicle penetrates into the accessible regions between the fibers and around the yarn bundle, since from visual observation, there is very little change in the size of the natural voids before or after coating the elastomer. The fluorochemical or fluorocarbon pretreatment on the other hand, does not permit the solvent to penetrate into the accessible region between the fibers and around the yarn bundle. Accordingly, the solvent/elastomer system coated on the fabric must remain at or near the surface. The only accessible region for the elastomer is the fiber bundle near the surface and the natural voids are filled to give the submicroscopic voids which give breathability while retaining the desired waterproofness and hand.
The drawings herein further illustrate the manner in which the fluorocarbon pretreatment functions to give the desired results. Thus, FIGURE 1 shows the fabric 2 with one surface (e.g. the outer face) coated with a fluorocarbon barrier layer 4. The opposite surface of the fabric carries a similar fluorocarbon barrier layer 6 with the waterproofing elastomer coating 8 thereover. FIG- URE 2 illustrates the case where no fluorocarbon pretreatment is used. In this situation, the entire fabric 10 is deeply penetrated and more or less saturated with elastomer as shown by the shading resulting in a product having poor hand.
It will be appreciated that various modifications may be made in the invention described herein while remaining within the scope of the invention as defined in the following claims wherein we claim:
1. A coated fabric suitable for rainwear which is breathable and waterproof and 'having substantially the appearance and hand of an uncoated fabric, which comprises a fabric, a first coating on said fabric of a fluorochemical having an oil rating of at least 70, a second coating thereon of a waterproof curable polymer, said first fluorochemical coating being at least partially disposed within the interstices of the fabric whereby the said second waterproof coating is prevented from substantially penetrating the said interstices and whereby said second coating lies substantially at or near the surface of the fabric.
2. The fabric of claim 1 wherein said curable polymer is a siloxane elastomer.
3. The fabric of claim 1 wherein said fluorochemical is selected from the group consisting of acrylates and methacrylates of hydroxyl compounds containing a highly fluorinated residue and their polymers and copolymers.
4. The coated fabric of claim 1 wherein the base layer of fabric has fluorochemical on both its sides and the waterproofing elastomer is on only one side.
5. The fabric of claim 1 wherein said fluorochemical coating has an oil rating of from -100.
6. A process for producing a textile fabric suitable for rainwear which is breathable and waterproof and having substantially the appearance and hand of an uncoated fabric, comprising depositing at least partially within the interstices of the fabric a fluorochemical having an oil rating of at least about 70, curing the fluorochemical, applying to the fabric a curable waterproofing polymer composition and curing said polymer composition, whereby the cured fluorochemical prevents substantion penetration of the uncured polymer into the interstices of the fabric.
7. The process of claim 6 wherein said composition is an elastomer in liquid vehicle, said composition being applied by knife coating.
8. The process of claim 6 wherein said composition is an elastomer in a liquid vehicle, said composition being applied by padding.
References Cited UNITED STATES PATENTS 2,191,362 2/1940 Widrner et al 117-1355 2,318,429 5/1943 Smith 117-1355 X 2,642,416 6/1953 Ahlbrecht et al. 117-136 X 2,673,823 4/1954 Biefeld et al. 117-1355 X 2,759,900 8/1956 Caldwell et al. 117-1355 2,802,754 8/1957 Ashby et al. 117-76 2,803,615 8/1957 Ahlbrecht et al 260-296 2,825,711 4/1958 Mayfield 117-1355 X 2,826,564 4/1958 Bovey et al. 260-835 2,839,513 6/1958 Ahlbrecht et a1 260-861 2,872,428 2/1959 Schroeder 117-1355 X 3,076,726 2/1963 Ault et al 117-161 X 3,081,193 4/1963 Stasse 117-76 X WILLIAM D. MARTIN, Primary Examiner. T. G. DAVIS, Assistant Examiner.

Claims (1)

1. A COATED FABRIC SUITABLE FOR RAINWEAR WHICH IS BREATHABLE AND WATERPROOF AND HAVING SUBSTANTIALLY THE APPEARANCE AND HAND OF AN UNCOATED FABRIC, WHICH COMPRISES A FABRIC, A FIRST COATING ON SAID FABRIC OF A FLUOROCHEMICAL HAVING AN OIL RATING OF AT LEAST 70, A SECOND COATING THEREON OF A WATERPROOF CURABLE POLYMER, SAID FIRST FLUOROCHEMICAL COATING BEING AT LEAST PARTIALLY DISPOSED WITHIN THE INTERSTICES OF THE FABRIC WHEREBY THE SAID SECOND WATERPROOF COATING IS PREVENTED FROM SUBSTANTIALLY PENETRATING THE SAID INTERSTICES AND WHEREBY SAID SECOND COATING LIES SUBSTANTIALLY AT OR NEAR THE SURFACE OF THE FABRIC.
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Cited By (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3462295A (en) * 1966-02-17 1969-08-19 Gen Mills Inc Process for rendering cellulosic and fibrous materials oil - water - repellent and product therefrom
US3462294A (en) * 1968-02-29 1969-08-19 Deering Milliken Res Corp Coating
US3502537A (en) * 1966-01-04 1970-03-24 Bondina Ltd Air-permeable protective materials
US3575103A (en) * 1968-08-19 1971-04-13 Ray E Charles Refuse compaction handling equipment utilizing fluids under low pressure
US3646749A (en) * 1969-12-24 1972-03-07 King Seeley Thermos Co Machine-washable metallized fibrous article and method of making same
US4265962A (en) * 1976-12-20 1981-05-05 Burlington Industries, Inc. Low penetration coating fabric
US4613544A (en) * 1984-12-04 1986-09-23 Minnesota Mining And Manufacturing Co. Waterproof, moisture-vapor permeable sheet material and method of making the same
US5698303A (en) * 1988-03-14 1997-12-16 Nextec Applications, Inc. Controlling the porosity and permeation of a web
US5846604A (en) * 1988-03-14 1998-12-08 Nextec Applications, Inc. Controlling the porosity and permeation of a web
US5856245A (en) * 1988-03-14 1999-01-05 Nextec Applications, Inc. Articles of barrier webs
US5874164A (en) * 1988-03-14 1999-02-23 Nextec Applications, Inc. Barrier webs having bioactive surfaces
US5876792A (en) * 1988-03-14 1999-03-02 Nextec Applications, Inc. Methods and apparatus for controlled placement of a polymer composition into a web
US5912116A (en) * 1988-03-14 1999-06-15 Nextec Applications, Inc. Methods of measuring analytes with barrier webs
US5935637A (en) * 1989-03-10 1999-08-10 Nextec Applications, Inc. Method of feedback control for the placement of a polymer composition into a web
US5954902A (en) * 1988-03-14 1999-09-21 Nextec Applications, Inc. Controlling the porosity and permeation of a web
US5958137A (en) * 1989-03-10 1999-09-28 Nextec Applications, Inc. Apparatus of feedback control for the placement of a polymer composition into a web
US6040251A (en) * 1988-03-14 2000-03-21 Nextec Applications Inc. Garments of barrier webs
US6071602A (en) * 1995-06-07 2000-06-06 Nextec Applications, Inc. Controlling the porosity and permeation of a web
US6083602A (en) * 1988-03-14 2000-07-04 Nextec Applications, Inc. Incontinent garments
WO2001046505A2 (en) * 1999-12-23 2001-06-28 Kimberly-Clark Worldwide, Inc. Nonwoven webs having liquid impermeability
US6312523B1 (en) 1988-03-14 2001-11-06 Nextec Applications, Inc. Apparatus of feedback control for the placement of a polymer composition into a web
US20030008585A1 (en) * 1995-03-21 2003-01-09 Hi-Tex, Inc. Treated textile fabric
US6541138B2 (en) 1996-08-07 2003-04-01 Hi-Tex, Inc. Treated textile fabric
US20040134045A1 (en) * 2001-05-12 2004-07-15 Konstantinos Poulakis Method for producing a touch-and-close fastener element
US20050181691A1 (en) * 2004-02-18 2005-08-18 Milliken & Company Dual function fabrics and method of making same
US20070021019A1 (en) * 2005-07-21 2007-01-25 Hi-Tex, Inc. Treated textile fabric
US20070231573A1 (en) * 2006-03-29 2007-10-04 Chapman Thermal Products, Inc. Fire retardant and heat resistant yarns and fabrics treated for increased strength and liquid shedding
US20100071119A1 (en) * 2006-03-29 2010-03-25 Chapman Therman Products, Inc. Yarns and fabrics that shed liquids, gels, sparks and molten metals and methods of manufacture and use
US20110145984A1 (en) * 2009-11-30 2011-06-23 Chapman Thermal Products, Inc. Methods of protecting a person from hot high heat capacity materials and hot corrosive material
US9630031B2 (en) 2006-03-29 2017-04-25 Chapman Thermal Products, Inc. Lightweight protective fabrics and clothing for protection against hot or corrosive materials

Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2191362A (en) * 1936-06-27 1940-02-20 Ciba Products Corp Treatment of textile materials
US2318429A (en) * 1940-08-03 1943-05-04 Du Pont Aqueous dispersion of polymerized alkyl methacrylate and method of preparing same
US2642416A (en) * 1950-05-26 1953-06-16 Minnesota Mining & Mfg Fluorinated acrylates and polymers
US2673823A (en) * 1949-08-26 1954-03-30 Owens Corning Fiberglass Corp Method of producing vapor permeable fluid impermeable fabric and product
US2759900A (en) * 1954-12-23 1956-08-21 Eastman Kodak Co Textile coating compositions containing polyacrylates with carboxyalkyl ethers
US2802754A (en) * 1956-10-31 1957-08-13 Gen Electric Water-repellent cotton textiles
US2803615A (en) * 1956-01-23 1957-08-20 Minnesota Mining & Mfg Fluorocarbon acrylate and methacrylate esters and polymers
US2825711A (en) * 1954-06-28 1958-03-04 Du Pont Plastisol compositions, process of preparing same, water vapor permeable coated fabrics prepared therefrom and processes therefor
US2826564A (en) * 1953-12-21 1958-03-11 Minnesota Mining & Mfg Fluorinated acrylates and polymers
US2839513A (en) * 1956-07-25 1958-06-17 Minnesota Mining & Mfg Fluorinated acrylate esters and polymers thereof
US2872428A (en) * 1955-01-31 1959-02-03 Shell Dev Polyepoxide emulsions and method of treating textiles therewith
US3076726A (en) * 1960-05-23 1963-02-05 Dow Corning Siloxane coating method and article obtained therefrom
US3081193A (en) * 1960-01-21 1963-03-12 Ucb Sa Process for the treatment of polyamide fabrics

Patent Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2191362A (en) * 1936-06-27 1940-02-20 Ciba Products Corp Treatment of textile materials
US2318429A (en) * 1940-08-03 1943-05-04 Du Pont Aqueous dispersion of polymerized alkyl methacrylate and method of preparing same
US2673823A (en) * 1949-08-26 1954-03-30 Owens Corning Fiberglass Corp Method of producing vapor permeable fluid impermeable fabric and product
US2642416A (en) * 1950-05-26 1953-06-16 Minnesota Mining & Mfg Fluorinated acrylates and polymers
US2826564A (en) * 1953-12-21 1958-03-11 Minnesota Mining & Mfg Fluorinated acrylates and polymers
US2825711A (en) * 1954-06-28 1958-03-04 Du Pont Plastisol compositions, process of preparing same, water vapor permeable coated fabrics prepared therefrom and processes therefor
US2759900A (en) * 1954-12-23 1956-08-21 Eastman Kodak Co Textile coating compositions containing polyacrylates with carboxyalkyl ethers
US2872428A (en) * 1955-01-31 1959-02-03 Shell Dev Polyepoxide emulsions and method of treating textiles therewith
US2803615A (en) * 1956-01-23 1957-08-20 Minnesota Mining & Mfg Fluorocarbon acrylate and methacrylate esters and polymers
US2839513A (en) * 1956-07-25 1958-06-17 Minnesota Mining & Mfg Fluorinated acrylate esters and polymers thereof
US2802754A (en) * 1956-10-31 1957-08-13 Gen Electric Water-repellent cotton textiles
US3081193A (en) * 1960-01-21 1963-03-12 Ucb Sa Process for the treatment of polyamide fabrics
US3076726A (en) * 1960-05-23 1963-02-05 Dow Corning Siloxane coating method and article obtained therefrom

Cited By (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3502537A (en) * 1966-01-04 1970-03-24 Bondina Ltd Air-permeable protective materials
US3462295A (en) * 1966-02-17 1969-08-19 Gen Mills Inc Process for rendering cellulosic and fibrous materials oil - water - repellent and product therefrom
US3462294A (en) * 1968-02-29 1969-08-19 Deering Milliken Res Corp Coating
US3575103A (en) * 1968-08-19 1971-04-13 Ray E Charles Refuse compaction handling equipment utilizing fluids under low pressure
US3646749A (en) * 1969-12-24 1972-03-07 King Seeley Thermos Co Machine-washable metallized fibrous article and method of making same
US4265962A (en) * 1976-12-20 1981-05-05 Burlington Industries, Inc. Low penetration coating fabric
US4613544A (en) * 1984-12-04 1986-09-23 Minnesota Mining And Manufacturing Co. Waterproof, moisture-vapor permeable sheet material and method of making the same
US5912116A (en) * 1988-03-14 1999-06-15 Nextec Applications, Inc. Methods of measuring analytes with barrier webs
US5698303A (en) * 1988-03-14 1997-12-16 Nextec Applications, Inc. Controlling the porosity and permeation of a web
US5856245A (en) * 1988-03-14 1999-01-05 Nextec Applications, Inc. Articles of barrier webs
US5874164A (en) * 1988-03-14 1999-02-23 Nextec Applications, Inc. Barrier webs having bioactive surfaces
US5876792A (en) * 1988-03-14 1999-03-02 Nextec Applications, Inc. Methods and apparatus for controlled placement of a polymer composition into a web
US6312523B1 (en) 1988-03-14 2001-11-06 Nextec Applications, Inc. Apparatus of feedback control for the placement of a polymer composition into a web
US5846604A (en) * 1988-03-14 1998-12-08 Nextec Applications, Inc. Controlling the porosity and permeation of a web
US5954902A (en) * 1988-03-14 1999-09-21 Nextec Applications, Inc. Controlling the porosity and permeation of a web
US6129978A (en) * 1988-03-14 2000-10-10 Nextec Applications, Inc. Porous webs having a polymer composition controllably placed therein
US6040251A (en) * 1988-03-14 2000-03-21 Nextec Applications Inc. Garments of barrier webs
US6083602A (en) * 1988-03-14 2000-07-04 Nextec Applications, Inc. Incontinent garments
US5958137A (en) * 1989-03-10 1999-09-28 Nextec Applications, Inc. Apparatus of feedback control for the placement of a polymer composition into a web
US5935637A (en) * 1989-03-10 1999-08-10 Nextec Applications, Inc. Method of feedback control for the placement of a polymer composition into a web
US6289841B1 (en) 1989-03-10 2001-09-18 Nextec Applications, Inc. Method and apparatus for controlled placement of a polymer composition into a web
US6884491B2 (en) 1995-03-21 2005-04-26 Hi-Tex, Inc. Treated textile fabric
US20030008585A1 (en) * 1995-03-21 2003-01-09 Hi-Tex, Inc. Treated textile fabric
US6071602A (en) * 1995-06-07 2000-06-06 Nextec Applications, Inc. Controlling the porosity and permeation of a web
US6541138B2 (en) 1996-08-07 2003-04-01 Hi-Tex, Inc. Treated textile fabric
US20040018787A1 (en) * 1996-08-07 2004-01-29 Hi-Tex, Inc. Treated textile fabric
WO2001046505A2 (en) * 1999-12-23 2001-06-28 Kimberly-Clark Worldwide, Inc. Nonwoven webs having liquid impermeability
WO2001046505A3 (en) * 1999-12-23 2002-01-03 Kimberly Clark Co Nonwoven webs having liquid impermeability
GB2375723A (en) * 1999-12-23 2002-11-27 Kimberly Clark Co Nonwoven webs having liquid impermeability
US7445741B2 (en) * 2001-05-12 2008-11-04 Gottlieb Binder Gmbh & Co. Method for producing a touch-and-close fastener element
US20040134045A1 (en) * 2001-05-12 2004-07-15 Konstantinos Poulakis Method for producing a touch-and-close fastener element
US20050181691A1 (en) * 2004-02-18 2005-08-18 Milliken & Company Dual function fabrics and method of making same
US7517819B2 (en) 2004-02-18 2009-04-14 Milliken & Company Dual function fabrics and method of making same
US20090178205A1 (en) * 2004-02-18 2009-07-16 Klutz David S Method of making dual function fabrics
US7901733B2 (en) 2004-02-18 2011-03-08 Milliken & Company Method of making dual function fabrics
US20070021019A1 (en) * 2005-07-21 2007-01-25 Hi-Tex, Inc. Treated textile fabric
US7531219B2 (en) 2005-07-21 2009-05-12 Hi-Tex, Inc. Treated textile fabric
US20070231573A1 (en) * 2006-03-29 2007-10-04 Chapman Thermal Products, Inc. Fire retardant and heat resistant yarns and fabrics treated for increased strength and liquid shedding
US20100071119A1 (en) * 2006-03-29 2010-03-25 Chapman Therman Products, Inc. Yarns and fabrics that shed liquids, gels, sparks and molten metals and methods of manufacture and use
US9630031B2 (en) 2006-03-29 2017-04-25 Chapman Thermal Products, Inc. Lightweight protective fabrics and clothing for protection against hot or corrosive materials
US20110145984A1 (en) * 2009-11-30 2011-06-23 Chapman Thermal Products, Inc. Methods of protecting a person from hot high heat capacity materials and hot corrosive material

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