US2387394A - Coated fabric material - Google Patents

Coated fabric material Download PDF

Info

Publication number
US2387394A
US2387394A US314683A US31468340A US2387394A US 2387394 A US2387394 A US 2387394A US 314683 A US314683 A US 314683A US 31468340 A US31468340 A US 31468340A US 2387394 A US2387394 A US 2387394A
Authority
US
United States
Prior art keywords
coating
coated
plasticizer
product
parts
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US314683A
Inventor
William D Hedges
John C Lowman
Thomas J Kerr
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Columbus Coated Fabrics Corp
Original Assignee
Columbus Coated Fabrics Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Columbus Coated Fabrics Corp filed Critical Columbus Coated Fabrics Corp
Priority to US314683A priority Critical patent/US2387394A/en
Application granted granted Critical
Publication of US2387394A publication Critical patent/US2387394A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/507Polyesters
    • D06M15/51Unsaturated polymerisable polyesters
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/01Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
    • D06M15/03Polysaccharides or derivatives thereof
    • D06M15/05Cellulose or derivatives thereof
    • D06M15/07Cellulose esters
    • 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
    • Y10T442/2369Coating or impregnation improves elasticity, bendability, resiliency, flexibility, or shape retention of the fabric

Description

Oct 23, 1945." w. D. Hl-:DGEs ET A1.
vCOATED FABRIC MATERIAL Filed Jan. 19, '1940 LJ ak,
Patented Oct. 23, 19f15 e COATED FABRIC MATERIAL William D. Hedges, John C. Lowman, and Thomas J. Kerr, Columbus, Ohio, assigiiors to Columbus Coated Fabrics Corporation, Columbus, Ohio, a corporation of Ohio Application January 19, 1940, Serial No. 314,683
3 Claims.
This invention relates to coatings and more particularly to coated fabrics and the application of flexible coating on a base material which is adapted to be folded and flexed.
It is an object of this invention to provide a coated material which is highly flexible and wherein the final product can be folded or twisted without damaging the coating film.
Another object of this invention is to provide an improved method of coating fabric or other suitable base supporting material which can -be `dried to produce a tack-free durable material.
Another object is to produce alcoated fabric having a pyroxylin coating film which is of improved pliability and which retains its durability and flexibility for a longer period oftime than similar coated materials made heretofore.
Another object is to provide a coating applicable to flexible base material to provide a wear` resistant surface which does not become dull Aand brlttleupon aging and exposure to the elements.
Another object is to provide a method of applying multiple coating films upon a flexible base to build up a coated sheet material which will not become tacky or soften when heated for several hours atl85 to 200 degrees F.
Another object is to provide a coated flexible base material which is adapted for use in making furnishings which must withstand outdoor exposure, `such -as porch furniture, awnings, etc.
Another Object is to make a waterproof, ilexible coated fabric of improved durability and which resists checking, chalking or cracking for a longer period of time than similar coated material made prior to this invention.
A further object is to provide a multiple coated fabric base with coating `compositions plasticized withia maleic acid modified castor oil plasticizer.
These and other objects will be readily apparent from the following description taken in connection with the drawing.
'In the'drawing:
Figure 1 is a side elevation view, partly in sec- Figure 3 is a similar view as Figure 2, showing the intermediate application of a color coat between the base coat vand the clear coat;
Figure 4 is a similar cross sectional View as in Figures 2 and 3, illustrating the application of a color base coat and a clear coat .in the manufacture of a coated fabric product.
In the manufacture of coated fabric it has been conventional heretofore to plasticize the coating composition with castor oil, blown oil, dibutyl phthalate, tricresyl phosphate and the like, but coated materials prepared by the use of these coatings have been found to have either a low exudation temperature or upon aging lose their flexibility and rapidly dull and eventually f crack, requiring replacement. The use of blown tion,` illustrating diagrammatically the method of applying one or more coatings to a cloth or fabric base material;
`Figure 2 is an enlarged fragmentary cross secftion view showing the application of two base coats and a superposed clear coating ona fabric -base material;
oils somewhat overcomes the diliiculty with exudation ofthe softening or plasticizing agent but the product does not have the required ilexibility.
It has been discovered that fabrics, felted material and the like flexible base products may be given one or multiple applications of coating films `wherein-the coating comprises a maleic acid-glycol reacted castor oil constituent as the softener or plasticizer to produce a highly improved coated fabric material. Further, by the application of an oleoresinous or varnish drying coat over the coated fabric,`the material may be given a high gloss which is very durable on aging. Each of the under coating films is plasticized with the modified castor oil plrasticizing resinous product. Where the nal gloss coating iilm is an oleoresinous varnish it will not contain plasticizer. After applying the coating the material is thereafter dried to produce a coated fabric having a high exudation temperature which in general will show no exudation of the softener over the temperature ranges 'to which pyroxylin coated fabrics can be safely subjected.
As examples illustrating typical formulae of the plasticizing agent utilized in compounding the coating compositions for application to the flexible base material, the following are given:
Example I A mixture of 1'50 parts by weight of castor oil, 31 parts by weight of glycol and 50 parts by weight of maleic anhydride is heated together in. a lC'lCilQIl chamber, with or without stirring or blowing with CO2. at a temperature of approximately 230 degrees C. for 12 hours. The reaction chamber is preferably equipped with a stirrer, and provision is made for escape of the water formed during the reaction, while at the same time loss of glycol is prevented. When the product is heat treated for this length of time the produce is in the form of a gel. If it is desired to carry.v4
Eample II In this example, 400 parts by weight of castor oil, 26 parts by weight of diethylene glycol and 50 parts by Weight of maleic anhydride are mixed 4 together and heated as described under Example I. Using the same temperature in cooking, the time is reduced from 12 to 8 hours. The acid number and valcohol solubility of the final resinous product are affected by the same factors as are noted under Example I. In this case the final product has an acid number of about 9 without the use of CO2. By heat treating the resin for longer than 8 hours at a temperature between 200 and 250 degrees C. the final resinous product will be in the form of a diflicultly soluble gel.
Example III In this example, 800 parts by Weight of castor oil, 50 parts by weight of maleic anhydride and 26 parts by weight of glycol, preferably diethylene glycol, are mixed together and heated, as set out above in Example I. In this instance the cooking time is about 14 hours at 230 degrees C. The resinous product produced has an acid number of about 9. A longer cooking time will produce a substantially insoluble resin. Where the resin is to be cooked to produce a product having a high viscosity it is preferable to add toluol or xylol in sufficient amount while the resin is hot so as to prevent the product from going over into an insoluble state upon cooling. The resins made as described will continue to polymerlze at temperatures below 200 degrees C. and even below 100 degrees C. so that the introduction of solvent to prevent the polymerization from continuing so as to produce an insoluble solid gel is required.
' castor oi1 are mixed with 26 parts by weight of diethylene glycol and 50 parts by weight of maleic anhydride and the mixture heat treated as in the previous example. The time required. for cooking this batch is much longer than that for the previous example. It was found impossible to produce a gel from this combination even after cooking the resinous batch for 27 hours at 275 degrees C. The product, however, results in yielding a bodied oily resin having definite advantages as a plasticizer over raw castor oil.
It will be understood that the above formulations are merely illustrative of the modified castor oil product utilized as the plasticizer and that the speciiic ingredients and particular proportions set out in the examples may be varied and equivalent compounds used in place of the materials mentloned.
In the application of the coatingy to the cloth or fabric base, referring particularly to Figure 1, the material A to be coated is moved along over guide rolls I and the coating composition applied from a suitable container 2 onto a spreading roller 3 which evenly coats the fabric as it is moved along. Thereafter the coating is dried by passing the coated fabric through a drying oven 4. This oven preferably" comprises suitable means such as a fan 5 and electric heater means 6, for moving the heated air in contact with the coating and in a direction opposite to that of the movement of the fabric, as shown by the arrows in Figure 1. Each of the coatings is preferably dried at a temperature rangeof to 250 degrees F. for about three minutes, depending upon the composition, and thereafter the coated fabric is moved therealong and additional coats applied if desired. Upwards of 12 to 15 coats may be applied; ordilnarily, however, seven or eight coats are sufficient to provide a durable coated fabric.
As shown in Figures 2, 3 and 4, a base coat or filler B is applied to a fabric or flexible backing A and thereafter a color coat C over the base coat. Finally, if desired, a clear flexible varnish or lacquer coat Dis applied thereover producing a high gloss finish.
In general the higher viscosity platicizer compositions show less tendency to exude than the lower viscosity less polymerized plasticizing product. The plasticizer formulated using 800 parts of castor oil, a's illustrated in Example III, has a viscosity of approximately 450 centipoises, and in the formulation of Example IV using 1000 parts of castor oil, the viscosity of the nal product is approximately 60 centipoises.
Coated fabrics and similar iiexible backing material are made in accordance with this invention by applying one or more coatings comprising the plasticizer formulated according to that illustrated in Figures 1 to 4 so as to provide a durable flexible coated base product. Nltrocellulose or pyroxylin coated fabrics made in this way exhibit greater exibility and are more durable upon aging than coated fabrics made heretofore utilizing castor' oil as the plasticizer.
As typical examples of the formulae suitable for application to flexible backing material, the following are given:
Example V The solvent is that conventionally used in compounding nitrocellulose compositions and in this instance comprises `by Volume ethyl acetate 45 per cent, alcohol 321/2 per cent, hydrocarbon (toluol or xylol) 221/2 per cent. Different pigments may be used which are preferably ground in the nitrocellulose and plasticizer composition, such as is commonly done in a ball mill. If desired suitable driers may be incorporated to speed up the film formation, particularly where slow drying pigments are used. The addition of zinc preferably in the form of naphthanate will retard the drying' actionvof the fast drying pigments so that mixtures of zinc naphthanate with Nitrocellulose (1/2 sec. or `20-30 A `Butyl acetyl ricinoleate `,litrocellulose (1/2 sec. or 20-30 Pigment ascuas `other pigments which accelerate the drying of the coating may be made to control the final product.
The above ingredients are compounded in the conventional manner.` 'The cloth is then coated `with 'the coating composition and dried. Coated fabric made with this formulation does not `exude or soften at 190 degrees F. and its flexing sec. vislcosity) Plasticizer. (Example III) Plasticizer (Example IV) Pigment Superfloss (diatomaceous earth) The above coating composition is compounded as the pigment formulation of Example V and is :adapted for use in making garments, typewriter i covers and similar coated fabrics where the maplasticizer in making coated fabrics of this invention is as follows: i
Example VI I Parts by weight sec. vis-V 12.0 20.0 10.0 Solvent 45.0
The coating is compounded as in Example V cosity) Plasticizer (Example IV) and is similarly applied to the fabric or flexible Parts by weight backing and dried to provide a soft flexible coated Y material.
`As a typical formula for a base coating, the
. following may be used:
Example VIII `'I'he solvent `used is amixture of ethyl acetate,
` l alcohol `and hydrocarbon solventV as given above inl Example V. Other suitable solvent mixtures commonly utilized in compounding cellulose nitrate compositions may be used.
Where it is desired to apply varnish or oil dry ing coating over a pyroxylin coated fabric to give it a higher gloss and `pleasing appearance, it is essential that the plasticizer used in formulating `the base coat does notexude at the tempera- `ture at which `the varnish coating is applied and dried thereon. The coating compositions formulated as disclosed when employing the maleic anhydride-polyhydric modified .castor oil as a plasticizer for the` base coating provide an ideal base `over which oil varnish, oleoresinous, alkyd `resin or similar clear varnish orlacque'r lcompol l `sltions may be applied and dried. 'I'his 'is readily accomplished because the plastcizer does not exude during drying of the varnish at 1185 to 200 degrees F.
`A clear lacquer or resinous coating containin the improved plasticizer and suitable as a coating to be applied over the case is as follows:
Example IX Parts by weight `Nitrocellulose (1/.sec. or 20-30 sec. viscosity) 12.0
Drying cil modified alkyd resin 4.0
Plasticizer (Example III) 20.0
Solvent 45.0
Asoftener or plasticizer utilized in compounding the sizing or coating composition.` In4 this way an improved coated fabric Vor filament is provided which will exhibit a high degree of flexibility and freedom from exudation of softener vwhen the coated fabric is subjected to relativelyhgh temperatures such as `to 200 degrees 1i.`
When the resinous plasticizers herein disclosed are used to replace raw castor oil on a part-byweight basis the plasticized film is somewhat less pliable. If the plasticizing resin is used to replace only a portion of the castor oil a softer nlm results than when the resinous plasticizer aloneis employed, and the exibility oi: the coating is greatly increased and the exudation point of the plasticizer is raised materially. It has been found unexpectedly that when upholstering material vor the like coated fabric made according to this invention is aged, it retains its original properties better after it has `aged several months than a similar material made utilizing raw castor. oil as aplasticizer before it has aged. It is believed that this results from the influence of the pigment on the drying action of the resinous plasticizer which forms` a. gel and continues to plasticize the filament without weakening it, while in the case of raw castor oil `no such results are produced. Further, more of the resinous plasticizer disclosed `herein may be incorporated in the coating film Without encounter` ing exudation difficulties than is possible'uslng raw castor oil. In this way artificial leather may Having thus fully described our invention. what we claim as new and desire to secure by V Letters Patent is: l
.1. A coated product comprising a flexible base and a coating thereon, said coating comprising a nitrocellulose film forming constituent and a plasticizer comprising the reaction product of substantially 800 parts by weight of castor oil, substantially 50 parts by weight of maleic anhydride and substantially 26 parts by weight of diethylene glycol for a period of about 14 hours at a temperature of substantially 230 C., said reaction product being characterized by the fact that its acid number is about 9, and said coated product being characterized by the fact that it will retain `its pliability and flexibility at extremely low temperatures, that the coating thereon will not soften or exude at temperatures of from 185 to 200 F. and will not crack or spew when subjected to weathering.
2. A coated product comprising a flexible base and a coating thereon, said coating comprising a nitrocellulose lm forming constituent and a plasticizer comprising the reaction product of substantially 150 parts by weight of castor oil, substantially 50 parts by weight of maleic anhydride and substantially 31 parts by weight of glycol for a period of about 12 hours at a temperature of substantially 230 C., said reaction V.product being characterized by the fact that its acid number is about 9, and said coated product being characterized by the fact that it will retain its pliability and flexibility at extremely low temperatures, that the coating thereon will not soften or 'exude at temperatures of from 185 to 200 F. and will not crack or spew when subjected to weathering.
3. A coated product comprising a ilexible base and a coating thereon, said coating comprising a nitrocellulose film forming constituent and a plasticizer comprising the reaction product of substantially 800 parts by weight of castor oil, substantially 50 parts by weight of maleic anhydride WILLIAM D. HEDGEs. JOHN c. LOWMAN. THOMAS J. KERR.
US314683A 1940-01-19 1940-01-19 Coated fabric material Expired - Lifetime US2387394A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US314683A US2387394A (en) 1940-01-19 1940-01-19 Coated fabric material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US314683A US2387394A (en) 1940-01-19 1940-01-19 Coated fabric material

Publications (1)

Publication Number Publication Date
US2387394A true US2387394A (en) 1945-10-23

Family

ID=23220992

Family Applications (1)

Application Number Title Priority Date Filing Date
US314683A Expired - Lifetime US2387394A (en) 1940-01-19 1940-01-19 Coated fabric material

Country Status (1)

Country Link
US (1) US2387394A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2671456A (en) * 1951-09-20 1954-03-09 Abraham Y Schultz Footwear washing apparatus
US3158525A (en) * 1960-09-26 1964-11-24 Du Pont Resin coated unwoven fabric

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2671456A (en) * 1951-09-20 1954-03-09 Abraham Y Schultz Footwear washing apparatus
US3158525A (en) * 1960-09-26 1964-11-24 Du Pont Resin coated unwoven fabric

Similar Documents

Publication Publication Date Title
US2387394A (en) Coated fabric material
US1950417A (en) Wrinkle finish for flexible articles
US2331977A (en) Process for making soft materials for raincoats, etc.
US1955355A (en) Asphaltic coating compositions and materials coated therewith
US2268022A (en) Drying oil composition
US1818575A (en) Rubber-coated fabric and process of making it
US1986787A (en) Cellulose derivative composition
US2719090A (en) Heat fugitive yellow coating composition and process of making it and a film formed of it
US1976191A (en) Wrinkle resin finish
US1689892A (en) Wrinkling finish
US2387396A (en) Upholstering fabric
US2201892A (en) Leather finish
US2387395A (en) Air dry
US2316099A (en) Linoleumlike products
US1883408A (en) Wrinkle finish coating
US2897166A (en) Process for the preparation of coating of soft resins from polyisocyanates and compounds containing hydroxyl groups
US1990474A (en) Oil acid varnish and product coated therewith
US1936500A (en) Rubber coated fabric
US1933697A (en) Modified castor oils and coating compositions containing the same
US1795199A (en) Rubber-coated fabric
US1959363A (en) Coated material
US1942736A (en) Coating composition
US2455540A (en) Flexible wrinkle finish and process of making
US2417405A (en) Artificial leather product
US2003068A (en) Protective finish