Flame Retardant Textile Fabrics

Purely for safety purposes, flame retardance or flame resistance of a fabric is a highly desirable characteristic. Of many methods available for developing various levels of flame retardancy all possess a variety of disadvantages, the principal ones being the inability of the flame retardant material, or treatment, to last through laundering or dry cleaning operations. Another principal disadvantage of treatments of fabrics to develop this characteristic of flame retardance is the loss of hand in the substrate. The problem is greatly aggravated in some areas of handling, particularly where it is necessary to meet statutory requirements for flame retardance in garments. Their physical condition being in the form of a bundle of fine fibers invites and encourages the sustenance of a flame if one gets started in the fabric. That is, a large area of oxidation is presented to any flame which gets started.

It is accordingly a basic object of this invention to provide a method employing familiar techniques in the textile industry for the application of flame retardant materials to textile fibers, whether the fibers be in the form of woven cloth, knitted cloth or in the form of balls of the thread prior to being woven into the cloth.

It is another object of the invention to provide technique which can be melted with the dispersed dyestuff application techniques for rendering fabric flame retardant.

Other objects and advantages of the invention will in part be obvious and in part appear hereinafter.

The present invention relates to a novel approach to flame proofing disperse dyeable synthetic materials which entails a process similar to dyeing but using colorless pigments with flame retardant properties. The colorless pigments are highly brominated aromatic and cyclic aliphatic compounds, which are extremely heat stable, high melting solids, which in addition are easily pulverized by milling to any desired particle size, ranging from 1 to 2 microns in average diameter.

Once the particles of the brominated aromatic compounds have been reduced to the optimum size, they are dispersed in water, at any concentration, by slowly adding them to water under strong agitation with a high speed, high shear mixer. In some cases a strong surface active agent must be added to effect uniform and thorough wetting of the flame retardant particles. After addition of the solid has been completed, the resulting dispersion can be stabilized by adding small quantities of a protective colloid (commonly called thickener) such as carboxymethylcellulose, ethoxy- or methoxycellulose of selected molecular weight to achieve an optimum viscosity to prevent the fine particles from settling. The resulting milky, viscous paste remains stable for an indefinite length of time, if stored under normal storing conditions.

The dispersion obtained as described above, can be applied to disperse dyeable synthetic materials by exhaustion or padding techniques, normally employed to dye these materials. The dispersion, general preparation procedure of, as described above, will be referred to as "FR Dispersion".

The FR Dispersion can be applied by three different techniques:

I. Batch process, at atmospheric pressure in presence of dye carrier with or without a dye levelling agent, commonly known as atmospheric dyeing process;

II. Batch process, under pressure, with or without a carrier and/or levelling agent, commonly referred to as pressure dyeing process;

III. Continuous process, at atmospheric pressure without the use of carriers and or levelling agents, commonly called as the thermosol process.

This operation is normally performed by immersing the goods to be processed in water contained in a suitable vessel at room temperature, wetting them thoroughly in the same and then heating them to a predetermined temperature. At this point a dye carrier and, if necessary, a levelling agent, and any other desired auxiliary, are added. The goods are thoroughly wetted in this solution. At this point the FR Dispersion and the disperse dyestuffs, if necessary, are incorporated in any given order, at regular intervals to allow the solution to reach equilibrium. The solution containing the goods, which at all times are maintained in constant motion by mechanical means, is slowly heated to the boil and boiled for a prolonged period of time. A sample of the material is now pulled and checked for color and flammability. Adjustments, if needed, are now made and the bath cooled replaced with solution of a scouring agent, and the goods are scoured and rinsed.

The above described process mainly applies to textile materials, but is not exclusive for the same and can be used on staple, tow, continuous filament or spun yarns, piece goods, such as knits, woven, non-woven fabrics, carpets, continuous films and the like.

This operation is normally carried out on becks, jigs, skein dyeing machines, tow and staple dyeing machines and the like.

The dye carriers are normally water insoluble organic materials which can be made water dispersible or emulsifiable by addition of suitable emulsifying or dispersing agents. The best known carriers are trichlorobenzene, biphenyl, orthophenyl phenol, butyl benzoate, methyl naphthalene, dichlorobenzene, perchloroethylene and the like. The mechanism of dyeing with carriers has been extensively studied and many more or less well-founded theories have been voiced on the subject. However, the mechanism of carriers is inconsequential to the scope of this invention.

The term disperse dyestuff applies to finely divided pigmentary organic materials of micron or submicron particle size dispersed or dispersible in water under given conditions. These materials are known to impart color fastness under most conditions, to hard to dye materials. The brominated aromatic compounds used in this invention, are similar to disperse dyes in their physical characteristics and their behavior towards some synthetic materials in the respect of their absorptivity and fastness when applied to those materials as described above.

Another means of dyeing disperse dyeable materials is using hermetically closed vessels and raising the temperature above the atmospheric boiling point of water. This high temperature has an effect similar to the one exerted by dye carriers and the need for carriers to effect the dyeing operation is either completely eliminated or reduced to a minimum. Water at high temperature, normally around 125.degree. C., appears to have a similar carrier effect as the materials listed above have been found to have.

The equipment used in this case is similar to that described above for dyeing at atmospheric pressure, with the difference that in this case it is tightly closed. The machines most commonly used are the yarn package dyeing machine, Burlington Engineering's Pressure Beck, Gatson County's Jet Dyeing Machine and others based on the same pressure dyeing principle.

The carriers used in this case are similar or the same as used in atmospheric dyeing and the dyeing procedure is also much the same as above with the difference that the dye bath is heated to .+-.125.degree. C.

In this case again the FR Dispersions show the same behavior as disperse dyes and are absorbed by the disperse dyeable materials.

In the case of continuous application by the pad-dry-thermosol process, the brominated aromatic material must possess a melting point 20.degree.-30.degree. C., lower than the thermosol temperature employed, but the melting point must be 10.degree.-20.degree. C., higher than the drying temperature used. In addition the brominated compounds must not undergo decomposition at the thermosol temperatures and/or change its color, crystalline structure, etc., at those temperatures. The preferred brominated materials melt between 125.degree. C., and 175.degree. C., and remain stable, without discoloration and/or evaporation when heated to 250.degree. C., and maintained at this temperature for 5 minutes.

The brominated flame retardant, predispersed in water, is dissolved in a predetermined amount of water and the disperse dyes, if needed, and any auxiliary required, are added to this solution. The material to be treated is then dipped in this treating bath and the excess removed by squeezing it between two rollers. The wet material is then dried by passing it over a series of hot cans, between sets of infrared dryers, through a chamber with circulating hot air or any other means available for drying, at temperatures ranging between 100.degree. C., and 125.degree. C., for a period of time long enough to reduce the moisture content of the treated goods as close to zero as possible.

The goods thus treated are then baked at temperatures ranging between 200.degree. C., and 250.degree. C., immediately after drying or at any convenient time thereafter for periods of time between 1 minute and 3 minutes. This heat treatment, normally referred to as thermosoling, has the effect of melting the brominated materials and driving it into the core of the substrate resulting in a permanent fixation of the same. The brominated treating material must not sublime or evaporate at the thermosol temperatures, since condensation on colder surfaces of the thermosol machines and dripping onto the goods being treated will result in unwanted spotting of the same. The brominated materials must also not discolor at the thermosol temperatures since this will result in yellowing of white goods or shade change of dyed goods. The brominated compounds must also not interact with the disperse dyestuffs, any other auxiliary they are used in conjunction with and/or the material they are applied to, at room or elevated temperatures, since this might lead to severe color changes of the dyes, impaired yield, degradation of the substrate, corrosion of the machinery, etc.

The goods can now be soaped off in any convenient way, to remove surface or loose particles. This step is unimportant to the scope of the invention.

The process of this invention, is applicable to textile materials, in staple, tow, yarn, woven, non-woven, circular knitted, tricot knitted, raschel knitted, double knitted, crimped, texturized, flocked, tufted, etc., form to continuous films, sheets, etc., used for packaging, decorations, insulation, etc., and any other material dyeable by the pad-dry-thermosol process.

The chemical nature of the treated materials is a polymer obtained by condensation of terephthalic acid with a glycol, normally ethylene or propylene glycol, known under the generic name of polyester. The polymer might also be modified by copolymerization with other materials so as to achieve any desired special effect.

The flame retardant treatment thus applied will withstand any conventional way of cleaning, will not affect, hand, color, texture, appearance, etc., of the substrate, will not, if appropriate compounds are used, degrade by the action of sunlight, heat, moisture aging, bacterial action, etc., alone or in combination with each other.

The present invention also relates to a new method of flame retarding textile and related materials using a commonly employed method in pigment printing and dyeing, that is, through the use of a primary binder which serves as an adhesive to fasten the flame retardant to a given substrate. In addition this technique can also be employed to flame retard the said binders, which normally are emulsions of synthetic polymeric materials which are highly flammable and contribute to the flammability of flame retardant substrates.

The subject of the present invention consists of two basic elements, the flame retardant element and a binding element.

The film retarding element is a colorless highly halobrominated, organic compound, solid at room temperature, possessing high melting and decomposition points, which is easily reduced to an extremely small particle size by conventional means of grinding. The solid flame retardant material is reduced to a submicron or micron particle/size and suspended in water in a fashion similar to the preparation of pigment dispersions. In some cases, specially when extremely heat stable materials are used, a synergist which will contribute to render the halobrominated solids more heat unstable must be employed. This synergist must possess similar characteristics to the halobrominated flame retardant, that is, it is a micropulverized solid possessing good heat stability, finely dispersed in water. In addition it must react with the halobrominated flame retarder at combustion temperatures to form a gaseous non-flammable gas which will prevent oxygen from reaching the flaming substrate, thus impeding the oxidation process.

The second element used in this embodiment of the invention is an emulsion of a high molecular weight polymer, commonly referred to as latex. The polymer employed can be the result of polymerizing acrylic acid, methacrylic acid, acrylamide, methacrylamide, acrylonitrile, esters of acrylic and methacrylic acids, vinyl chloride, vinylidene chloride, styrene, butadiene, maleic or fumaric acids and esters of same and the like. The polymer can be homopolymers or copolymers of the above described monomers. These emulsion polymers are commercially available in differing grades depending on the ultimate properties desired. They have in common the fact that they form films at room or elevated temperatures, alone or in the presence of plasticizers. The properties of the film depending on the chemical composition of the same.

Due to the fact that the latexes possess extremely good adhesive properties, they are normally used for bonding purposes. They are used for bonding of pigments to hard to dye substrates, to bond fibers with fibers to obtain non woven fabrics, to bond fibers to fabrics to produce flocked fabrics and to bond fabrics to fabrics, fabrics to foams, fabrics to films, to non wovens, etc., to obtain laminated fabrics. They are also used for fabric backcoating to achieve various effects such as dimensional stability, to prevent ravelling, to give fabrics non slipping characteristics, with a filler, to impart opacity to the same, etc., and for finishing to achieve, dimensional stability, to increase strength, decrease air permeability, impart water repellency, etc.

This invention relates to two uses of these materials:

a. To bond the flame retarder to non reactive substrates by the use of latex adhesives; and

b. To use the flame retardant to make the latex films non-combustible or self extinguishing when they are applied to flame retarded substrates.

a. In this application the solid flame retardant is the predominant ingredient and the latex is the minor ingredient.

The micropulverized solid flame retardant is first dispersed in water containing a wetting agent by adding it slowly to the aqueous phase under strong agitation, with a high speed, high shear mixer. After addition of the solid has been completed, the resulting dispersion is stabilized by adding small quantities of a protective colloid (commonly called thickener) such as carboxy methyl cellulose, methoxy or ethoxycellulose of selected molecular weight to achieve an optimum viscosity and prevent the particles from settling.

The FR flame retardant is now diluted with water to a predetermined strength and sufficient amount of latex to achieve adhesion is added. This solution is now applied to the substrate by dipping it into this solution and removing the excess by squeezing between two rollers. The wet substrate is now air dried at any convenient temperature and baked at 125.degree. C. to 150.degree. C. for 180 to 90 seconds.

The resulting material is flame retardant when tested by commonly used flammability tests and the flame retardant is not lost after multiple launderings and/or dry cleanings. The feel or hand of the flame retardant material is unchanged, but can be made stiff, if desirable, by selecting a harder latex.

b. The FR dispersion prepared as described above, is diluted in water, the latex is added and the viscosity adjusted by the use of a thickener.

This treating batch is now applied by different techniques depending on the final effect desired. It can be padded, knife coated, roller coated, sprayed, roller printed, screen printed, applied by saturation and the like. The substrates are now air dried at any convenient temperature, and baked as above.

This technique is usually employed when the substrate to which the latex is applied is either intrinsically flame retardant or has been flame proofed in a separate operation. It can be used to flame retard latices, which will be employed as flocking adhesives, for fabric backcoating, pigment dyeing or printing, bonding or non woven fabric lamination and the like.

The process of this embodiment of the invention is applicable to textile materials, in staple, tow, yarn, fiber, woven fabrics, non-woven fabrics, circular and flat knits, carpets and the like, to paper, to films, to foams, etc.

The substrate can be of natural origin such as cotton, linen, jute, coco fiber, wool, silk and the like, man made such as regenerated cellulose, cellulose di and triacetates, fiberglass and the like or synthetic polymeric materials such as nylon, polyester, acrylics, polypropylene and the like.

The present invention utilizes brominated aromatic compounds, preferably brominated as flame retarding materials. The preferred aromatic compounds employed are derivatives of ##STR1##

Where A through N are the same or different and can be H, Br, CH.sub.3, C.sub.2 H.sub.5, C.sub.3 H.sub.7, ##STR2## C.sub.4 H.sub.9 and the like; and X, Y, Z can be the same or different and can be H, CH.sub.3, C.sub.2 H.sub.5, C.sub.3 H.sub.7, C.sub.6 H.sub.5, ##STR3## and the like, wherein N' and M' are the same or different and can be chosen among H, NH.sub.4, NH.sub.2, Na, K, Li, Ca, Mg, Ba, Sb, T, I, and the like.

Aliphatic cyclic compounds of the nature: ##STR4##

The preferred entities are:

1. Polybrominated benzenes of the general formula: ##STR5## where A' to F' are the same or different and may be H or Br, with at least one Br present on the benzene ring.

2. Polybromo monoalkyl benzene of the general formula: ##STR6## where R.sub.1 may be alkyl, preferably of 1-5 carbons such as methyl, ethyl, propyl, butyl, pentyl, isopropyl, tert butyl; unsaturated alkyls haloalkyl or polyhaloalkyl wherein the moiety may include up to four bromine atoms where the halogens are chlorine and/or bromine and A', B', C', D', E' are as defined in numbered paragraph 1 immediately preceding.

3. Polybromo dialkyl benzene of the general formula: ##STR7## where R.sub.1 and R.sub.2 are the same or different and are the same as R.sub.1 in numbered paragraph 2 immediately preceding.

4. Polybrominated phenols of the general formula: ##STR8## wherein A' to E' are as defined in paragraph 1, and wherein X' is H, R.sub.1, ##STR9## C.sub.6 H.sub.5, C.sub.6 H.sub.n X.sub.m "', wherein n is 1 to 4, X is Br and m varies between 1 to 5, where R.sub.3 and R.sub.4 are the same or different and can be H, alkyl preferably of 1-5 carbon atoms, bromoalkyl, polybromoalkyl and the like; aryl, phenyl, bromoaryl, bromophenyl, polybromoaryl, polybromophenyl, NH.sub.4, NH.sub.2, Na, K, Li, Ca, Ba, Sb, Ti and the like; or ##STR10## wherein R.sub.3 is as defined hereinabove.

5. Polybrominated biphenyls of the general formula: ##STR11## where A" to J" are the same or different and are H, Br, lower alkyl C.sub.1 to C.sub.5, aryl, ##STR12## X" being OH, NH.sub.2, ONH.sub.4, Na, K and the like.

6. Polybrominated terphenyls of the general formula: ##STR13## where A" to N" have the values assigned to A" to J" in numbered paragraph 5 hereof.

7. Polybrominated aniline of the general formula: ##STR14## where A" to E" have the values assigned to A" to N" in numbered paragraph 6 immediately preceding, and X" and Y" are H, lower alkyl C.sub.1 to C.sub.5, aryl, bromoalkyl, polybromoalkyl, bromoaryl, polybromoaryl, phenyl bromophenyl, polybromophenyl and the like.

8. Polybrominated aromatic mono and polyacids, anhydrides or esters of the same or the general formula: ##STR15##

9. Polybrominated bisphenol A of the general formula: ##STR16## wherein A" to H" have the values assigned in numbered paragraph 5 hereinbove; and R.sub.1 and R.sub.2 have the values assigned in numbered paragraph 3 above.

In the process of preparing the proofing agents of the present invention the polyhalogenated solid material is milled to a convenient particle size, ranging from 0.1 to 10 microns, using any suitable means such as pebble mills, hammer mills, and grinders, jet grinders and the like.

The water-insoluble organic bromine compound is present in one embodiment of the invention in a concentration of about 50 percent to about 75 percent. It is also true that the fine powder thus obtained is dispersed in 0.25 to 1 part, preferably, 0.3 to 0.4 parts of water containing a small amount (0.1 to 0.5%) of a nonionic wetting agent of the ethoxylated nonylphenol type. Using a high speed high shear mixer or blender, the dispersion is stabilized with a small amount of a protective colloid such as hydroxyethyl cellulose; 0.2 to 0.5% of the latter is normally sufficient.

The resultant product may be used in the concentration thus obtained or may be diluted with 0.5 to 10 parts of water to each part of the dispersion.

The substrate to be treated is immersed in the resultant dispersion which can also contain 5 to 30% of the weight of the goods of a dye carrier and then slowly heated to the boil if open equipment is used or to 110.degree.-140.degree. C., preferably 125.degree. C., if a sealed machine is used. This solution can also contain disperse dyestuffs as well as the flame retarder. This solution is now maintained at the desired temperature for 1-5 hours, preferably 1-2 hours allowing the dyes and the flame retardant to exhaust uniformly onto the substrate being treated.

After the operation has been completed the treating solution is cooled to room temperature and discarded. The goods are then rinsed to remove any surface deposits and dried by any convenient means at any convenient temperature.

Another means of applying the fire retardant is by dipping the substrate to be treated in a solution containing 5-50%, preferably 10-25%, of the concentrated flame retardant dispersion insuring complete and even impregnation and the excess solution removed, suitably by pressing between two rollers or the like. The treated substrate is then air dried at between 100.degree. and 120.degree. C., and baked between 175.degree. and 225.degree. C., for 30 to 120 seconds.

The substrates which might be treated by this method include all synthetic thermoplastic materials which are dyeable with disperse dyestuffs, which include polyester, polypropylene, polyethylene, cellulose di and tri acetates.

The substrate to be treated may be in the form of staple, tow, filaments, yarn, thread, continuous fiber, woven, knitted and non-woven fabrics, carpet, sheets, films and the like. The quantities to be used will vary depending on the construction of the material, its flammability and the flame retardant specification to be met.

In the process of preparing the flame proofing agent of the present invention, there is also utilized a synergist which reacts with the halobrominated organic material at the flame temperatures inducing its decomposition and liberating a non-flammable gas which forms a blanket around the flaming substrate, displacing the oxygen from the vicinity of the same thus impeding the oxidation process of the combustion.

The synergists are normally metallic oxides of the general formula:

where Me can be Al, Ga, Si, Ge, As, Sb, Bi, Ti, Zr, and the like and n is the valence of the metal in its oxidized state. Especially are the oxides of aluminum, germanium, antimony and titanium useful.

These oxides must also be present in a fine particle state of the same size as the halobrominated compound or smaller.

The synergist is blended with the halobrominated compound during the preparation of the FR dispersion, the ratio of halobrominated compound to synergist depending on the stability of the halobrominated material and the reactivity of the particular metallic oxide employed. It was found that normally 3 to 7 parts halobrominated flame retarder for each part of metalllic oxide, preferably 4-6 parts to 1 part, give the best results.

The emulsion polymers, commonly referred to as synthetic latices in one embodiment of the invention, are commercially available materials, obtained by emulsion homo- or co-polymerization of monomers of the general class: ##STR17## where R.sub.1 and R.sub.2 can be the same or different and can be selected among H, Cl, Br, CH.sub.3, CnHm where n is 1 to 5 and m=2n+1, COOH, CONH.sub.2, CN, CH.dbd.CH.sub.2, C.sub.6 H.sub.5 and the like.

The preferred monomers are alkyl esters of acrylic and methacrylic acids, acryl and methacryl amides, acrylonitrile, acrylic and methacrylic acids, maleic or fumaric acids and alkyl esters of the same vinyl and vinylidene chlorides, styrene and butadiene.

Due to the infinite number of possible combinations we will class the polymers in the following groups:

a. Acrylic latices, mainly homo-or-co-polymers of alkyl esters of acrylic or methacrylic acids which can also contain acrylic or methacrylic acid acrylonitrile, acrylamide, n-methylol acrylamide, vinyl and vinylidene chlorides and the like. The alkyl group of the esters can also contain hydroxyl groups. The presence of reactive groups, such as HO, CONH.sub.2, COOH, ##STR18## suggests the possibility of further crosslinkage of the effect of heat leading to a higher molecular weight and thus much more stable polymers. These type of polymers are referred to as cross-linking, self-cross linking or thermosetting latices.

b. Acrylonitrile Latices: where the major ingredient is acrylonitrile which can be found as homo polymers or copolymers as in a.

c. Vinylchloride Latices: where the major constitutent is this monomer homo-polymerized or copolymerized as in a.

d. Vinylidene chloride latices;

e. ABS (acrylonitrile-butadiene-styrene) latices; where these three monomers are the principal ingredients and can also be copolymerized with other monomers as in a.

f. SBR (styrene-butadiene-rubber) latices.

g. Also there are employed emulsion polymers obtained by the reaction of a polyisocyanate and an aliphatic polyol which can be a polyether, a polyester, or a polycaprolactone, the preferred polyisocyanate being a mixture of isomers of toluene diisocyanate and the preferred polyol being a polyethylene glycol condensate having a molecular weight in excess of 3,000 commonly referred to as a polyurethane latex.

The reason for blending these various monomers is to achieve polymers with varying film properties, such as:

1. Feel or hand of film. This can vary from soft to hard and from tacky or dry. This parameter is measured by the glass transition temperature (T.G.) or in some cases by T.sub.300 (temperature at which the torsional modulus of an air dried film is 300 Kg/CM.sup.2). Both are measured in .degree.C. and can range from -100.degree. C. to +100.degree. C. As a general rule, the lower the TG or T.sub.300 the softer the film, the film becoming harder with increasing temperatures.

2. Solvent swelling resistance. Latices are known to swell when wetted with organic, specially chlorinated solvents, resulting in lack of durability to dry cleaning. This property is improved by introducing crosslinkable sites into the molecule of the polymer.

3. Film strength. The strength of the film is also improved by increasing the molecular weight of the polymer through the introduction of crosslinkable sites which are made to react by heat and/or catalysts.

4. Adhesion of film. This property is very important since the durability of the flame retarder will greatly depend on it.

In the process of preparing the flame retardant dispersion, 1 to 4 parts, preferably 2 to 3 parts, of a finely divided powdered halobrominated organic material is dispersed in 1 part of water containing 0.1 to 1% of anionic wetting agent by the use of a high shear mixer. After addition is completed 0.1 to 1 part, preferably 0.2 to 0.4 parts, based on the weight of the halobrominated organic compound of a metallic oxide is slowly added. After addition is complete the dispersion is stabilized by adding 0.1 to 0.5%, preferably 0.2 to 0.3%, on the weight of the dispersion of a protective colloid such as ethoxy cellulose.

In the case when it is necessary to flame retard a given substrate 0.5 to 1.5 parts, preferably 0.8 to 1.2 parts, of FR dispersion are dissolved in 1 part of water with mild agitation. To this solution, 0.05 to 0.4, preferably 0.1 to 0.3 parts of a latex containing 35 to 65%, preferably 45 to 55%, of a polymer is added. In treating hydrophobic substrates, 0.5 to 1.5%, preferably 0.8 to 1.2% of a wetting agent is added.

The substrate to be treated is dipped in this solution and the excess removed by squeezing between two rollers. The wet material is air dried in an oven at 80.degree. C. to 130.degree. C., preferably 100.degree. C. to 110.degree. C., and baked at 140.degree. C. to 180.degree. C., preferably 150.degree. C. to 170.degree. C. for 1/2 to 5 minutes, preferably 11/2 to 3 minutes.

When the substrate to be treated is either intrinsically flame resistant or has been flame retarded in a separate operation and must be treated with a flammable latex to achieve some desirable effect on the substrate the treating solution is prepared as follows: To 1 part of water 0.5 to 1.5 parts, preferably 0.8 to 1.2 parts, of latex is added, and the solution is mixed until uniform. 0.05 to 0.2 parts, preferably 0.1 to 0.15 parts, based on the weight of the latex of FR dispersion is added and mixed to uniformity. At this point any other needed auxiliaries, such as pigments, thickeners, fillers, plasticizers, wetting agents, catalysts, and the like, are incorporated in any required proportion and the solution mixed.

The treating solution is now applied to the flame resistant substrate any any convenient way, such as padding, coating, printing, saturation and the like and the wet goods are dried and baked as above.

70 parts of finely pulverized hexabromo benzene having an average particle size of 1.5 microns were slowly added to 30 parts of water, under rapid agitation, containing 0.25% of an ethoxylated nonyl phenol type wetting agent. After addition was completed the agitation was continued for an extra 15 minutes. To this dispersion 10 parts of a 4% hydroxyethyl cellulose solution in water having a viscosity of approximately 300,000 centipoises were added and the resulting dispersion was agitated for an additional 15 minutes. This dispersion was designated I.

A piece of a spun woven polyester fabric weighing 10 grams fastened to a rod was immersed in 150 milliliters of water at room temperature with a pH of 6.0 adjusted with monosodium phosphate contained in a beaker. This beaker was placed in an oil bath. The rod was now attached to a mechanism which imparted an up and down motion at a rate of 20 strokes per minute. The oil bath was now heated by means of an electrical resistance until the temperature of the water reached 50.degree. C. Heating was now interrupted and 2.5 grams of self-emulsifiable biphenyl predissolved in 2.5 grams of water at 50.degree. C. were added as a swelling agent. This solution was maintained at 50.degree. C. for 10 minutes to allow the biphenyl to penetrate the fabric. At this point 2 grams of dispersion I and 1 gram of disperse Blue 1 (color index #42025) were added. This solution was now heated, at a rate of 0.5.degree. C., per minute, to the boil. The bath was maintained at the boil for 2 hours. At this point the beaker was removed from the oil bath and placed in a cooling bath. The rod with the fabric was removed from the beaker and rinsed using running water at room temperature. The fabric was removed from the rod and dried in an oven at 105.degree. C.

The fabric was now folded and sewn with a non flame retarded cotton thread to form a seam. The flammability along the seam was now tested using method DOC FF3-71 giving a void area of 1.5 inches initially and 2.0 inches after 50 launderings and tumble dryings. A similar fabric non flame retarded was consumed entirely when tested by this method.

70 parts of finely pulverized tetrabromo ortho chlorotoluene having an average particle size of less than 2 microns was dispersed in water in the same manner as dispersion I. This dispersion was designated II.

A piece weighing 10 grams of a tufted polypropylene carpet with a jute backing was treated similarly as in Example I, but using 1.0 grams of dispersion II. After dyeing cycle was completed the carpet was dried at 80.degree. C. until dry.

The dyed carpet exhibited approximately 10% less color than a sample dyed similarly but without the flame retardant.

The flammability of the treated carpet was tested using flammability standard for carpets and rugs DOC FF1-70, giving a burn 1 inch in diameter, whereas the control carpet was totally consumed when tested by this procedure.

70 parts of pulverized tris tribromophenyl phosphate having a particle size less than 2 microns was dispersed in water in the same fashion as dispersion I.

A package of 100% polyester filament yarn weighing approximately 1,000 grams, wound on a spring type tube, was placed in a closed vessel equipped with a heating element and a centrifugal pump which would pump liquid through the center to the periphery of the package. A funnel type vessel equipped with a valve is connected to the inlet of the pump. This is used to make additions of chemicals and/or dyes. The vessel containing the package was covered with a lid which was then fastened tightly with bolts.

Approximately 8 liters of water at room temperature were pumped into the dye vessel with this liquid circulating through the package. The water was heated to 110.degree. C. and the pH adjusted to 6.0 with monosodium phosphate. The liquid was circulated for 5 minutes at the same temperature. At this point 50 grams of disperse yellow #3 (color index #11855) pasted in 50 grams of water containing 0.1% dispersing agent were allowed to flow into the dye chamber. This solution was allowed to circulate through the package for 5 minutes. At this point 50 grams of dispersion III were added and the solution circulated for 5 minutes. 50 grams of self-emulsifiable 1,3,4 trichlorobenzene were now added and heating was begun at a rate of 1.degree. C. per minute until a temperature of 121.degree. C. was reached. The solution was maintained at this temperature for 60 minutes and then allowed to cool to 70.degree.-80.degree. C. when it was discharged and replaced with water containing 1 gr/lt tetrasodium pyrophosphate 1 gr/lt sodium hydrosulphite and 0.5 grs/lt non-ionic detergent at 70.degree. C. and with this liquid circulating through the yarn package the temperature was raised to 100.degree. C. and maintained at the same for 20 minutes. The scouring solution was now discharged and replaced with water at 50.degree. C. The water was drained off, the package removed from the vessel and air dried in an oven at 105.degree. C.

The yarn from the package was now knitted into a sock, a fold was made in this sock which was stitched with a sewing machine using non-flame retarded cotton thread resembling a seam and the flammability was tested alng this seam following method described in DOC FF3-71, flammability of children's sleepwear. The sample treated as described above gave a void area of 21/2 inches, while a sample dyed under the same conditions, but without dispersion was consumed in its entire length. No difference in coloration was seen when both samples were compared visually.

70 parts of hexabromo biphenyl having an average particle size of 2 microns and a melting point between 136.degree. C. and 150.degree. C. was dispersed in 30 parts of water in the same fashion as dispersion I. This suspension was designated dispersion IV.

20 parts of dispersion IV were dissolved in 80 parts of water and 0.5 parts of an alkyl-aryl sulfonate wetting agent were added to this solution.

A piece of 100% polyester double knit fabric was immersed in this solution and the excess removed by squeezing it between two rollers. The fabric picked up 110% of its weight of the solution and was now air dried in an oven at 105.degree. C. The particles of hexabromobiphenyl were noticeable on the surface and would become loose on shaking the fabric. The treated material was now baked at 200.degree. C. for 90 seconds in a forced air oven. The banking had the effect of melting the flame retardant and driving it into the core of the fiber. No dusting off was observed after the baking operation.

The treated fabric was judged flame retardant when tested according to standard for the flammability of children's sleepwear DOC FF3-71.

In recapitulation, it will be apparent from inspection of the examples that my technique for rendering a fabric flame retardant is to disperse it in the fabric. In so doing I formulate the flame retarding material in an extremely fine particle size suspended in an aqueous medium with a protective colloid material so that a solution or dispersion of this can be used for padding of the material. Generally the materials used will be in the form of fibers, but fabrics are also contemplated. The end result is that the extremely fine particles enter the fibers and on drying of the paste in which they are incorporated, or mere aqueous suspension in which they are used, they are mechanically included within the surface of the fiber itself, there to function as the flame retardant. To obtain maximum dispersion I have found that particle size of 0.10 micron or smaller is desirable but that particle sizes up to 3 microns average particle diameter, are useful. Generally, the one to 2 micron range is preferred.

When I speak of particle size I speak of the average in statistical terms. This is measured either in a Colter Counter or a Fisher Counter, or a microscopic measurement. Also sedimentation rates are sometimes used. The techniques for accomplishing such measurements are generally quite well known among chemists and need not be set forth herein in detail.

An inherent fundamental requirement of the process however is that the material used as the flame retardant be a highly insoluble compound. Hence, ideally, the flame retardant material will show a statistical particle size wherein about 90% or more of the particles will be under 2 microns in diameter.

If the particles could be reduced to less than one micron, in diameter, it would be advantageous in the fabric and thus would not cause loss of luster.

As suspending agents, various organic protective colloidal materials soluble in water are useful. For example, the Cellosize materials, and ethoxy cellulose, methoxy cellulose and other carboxyalkyl celluloses are quite useful. Polyvinylacetate is useful also. Generally, any colloidal protective material which is virtually inert on a fabric and serves to hold the materials in suspension will be useful.

I have specified that the material should be highly insoluble. Basically, the more insoluble the material the better. Generally, I prefer to confine the use of the flame retardants to those showing insolubility of less of 1/10th part per 1000 parts of solvent.

70 parts of finely divided decabromo biphenyl possessing an average particle size between 1 and 2 microns was slowly added to 50 parts water containing 0.2% anionic wetting agent of the alkyl-aryl sulfonate type, under strong agitation with a high speed, high shear mixer. After completing the addition of the brominated compound 12 parts of finely divided antimony-trioxide possessing an average particle size between 1 and 2 microns were slowly added while agitation was continued. After all the antimony-trioxide was added the resulting milky white dispersion was stabilized by addition of 5 parts of a 4% aqueous solution, having a viscosity of 300,000 centipoise, of ethoxycellulose. This dispersion, thus obtained, remained uniform after prolonged storage at room temperature and was designated dispersion V.

50 parts of dispersion V were now dissolved in 40 parts of water and 10 parts of a 50% aqueous emulsion of a copolymer of ethyl acrylate and acrylamide having a T.sub.300 of -47.degree. C. were added.

A woven fabric weighing 4 ozs. per square yard composed of 50% cotton and 50% polyester was now treated with this solution by immersing it in the same and removing the excess by squeezing between two rollers. The wet pick-up was 90%. The fabric was now dried at 110.degree. C. and baked at 150.degree. C. for 3 minutes.

The fabric thus obtained was quite soft to the feel and was further softened by padding it through a 10% emulsion of polyethylene softener in water.

The flame resistance of the fabric thus treated was evaluated by testing according to the test method given in "Standard for the Flammability of Children's Sleepwear" DOC FF3-71 giving an initial average char length of 11/2 inches and 2 inches after 50 launderings and tumble dryings.

70 parts of finely divided hexabromo benzene having an average particle size between 1 and 2 microns were dispersed in 50 parts of water in a similar fashion to dispersion V. 15 Parts of aluminum oxide were added to the dispersed brominated compound and this dispersion was stabilized as dispersion V. This material was designated dispersion VI.

40 Parts of dispersion VI were dissolved in 52 parts of water and 8 parts of a 50% emulsion of a styrene butadiene copolymer having a glass transition temperature of -80.degree. C. were added.

A piece of 100% cotton circular knit weighing 8 ozs/yd.sup.2 were immersed in this solution and the excess removed by squeezing between two rollers. The wet pick-up was 120% and the fabric was dried at 110.degree. C. and baked at 150.degree. C. for 3 minutes. The fabric was softened by padding through a 10% emulsion of a polyethylene softener and dried.

The fabric was judged flame retardant by using method outlined in DDC FF3-71, giving an initial average char length of 1 inch and 21/2 inches after 50 launderings and tumble dryings.

70 Parts of finely divided pentabromo toluene and 20 parts of titanium dioxide having an average particle size of between 1 and 2 microns were dispersed in 50 parts of water as in Example V. This dispersion was designated dispersion VII.

50 Parts of dispersion VII were dissolved in 40 parts of water and 10 parts of a 50% acrylonitrile-styrenebutadiene latex having a glass transition temperature of -60.degree. C. were added to this solution. The resulting mixture was padded onto a woven fabric composed of 80% rayon and 20% cellulose diacetate in a similar fashion as in Examples V and VI. The fabric was dried at 110.degree. C., baked at 150.degree. C., top softened with a 10% emulsion of a polyethylene softener and redried.

The treated fabric gave an average char length of 3 inches initially, when tested according to AATCC Flammability Test 34-1967, an average char length of 4 inches after 5 launderings and tumble dryings and an average char length of 5 inches after 5 commerical dry cleanings.

70 Parts of Tris dibromophenyl phosphate and 10 parts of antimony trioxide having an average particle size between 1 and 2 microns were dispersed in 40 parts of water as in Example V. This dispersion was designated dispersion VIII.

50 Parts of a 50% emulsion of a butyl acrylate-N-methylol acrylamide-acrylonitrile copolymer latex having a glass transition temperature of 0.degree. C. were dispersed in 30 parts of water. To this solution 10 parts of a 50% aqueous dispersion of disperse blue 1 (color index #42025) and 10 parts of dispersion VIII were added and the resulting mixture agitated until uniform.

A 100% woven fiberglass drapery fabric was immersed in this solution, the excess removed by squeezing between two rollers to obtain a wet pick-up of 50%, dried at 110.degree. C. and baked at 150.degree. C. for 3 minutes.

This fabric gave an average char length of 3 inches when tested using AATCC flammability test 34-1967, after 5 launderings and tumble drying and 5 commerical dry cleanings.

70 Parts of finely divided tribromoaniline and 15 parts of micropulverized aluminum trioxide having a particle size of between 1 and 2 microns were dispersed in 50 parts of water following procedure given in Example V. This dispersion was designated as dispersion IX.

0.5 Parts of tetrasodium pyrophosphate were dissolved in 14.5 parts of water. Under strong agitation 10 parts of a finely divided clay and 5 parts of dispersion IX were added. Upon completion of the addition 45 parts of a 50% aqueous emulsion of a polymer obtained by the copolymerization of ethyl acrylate, n-methylol acrylamide, acrylonitrile and acrylic acid having a glass transition temperature of -2.degree. C. were mixed in. The viscosity of this dispersion was adjusted to 35,000 centipoises by adding 24 parts of a 4% solution of methoxy cellulose. Finally, 1 part of a 10% solution of oxalic acid (acid catalyst) was mixed into this dispersion. This dispersion was designated IX-A.

A piece of the 80% rayon 20% cellulose diacetate fabric treated in Example VII was coated on one side with dispersion IX-A using a doctor blade to a loading of 70% on the weight of the fiber. The fabric was dried at 125.degree. C. and cured at 160.degree. C. for 2 minutes.

The fabric thus treated gave a char length of 3 inches when tested according to AATCC method 34-1967, initially after 5 launderings and 5 dry cleanings. The same fabric coated with the same composition, but without dispersion V was consumed entirely when tested by this flammability method.

70 Parts of finely pulverized tetrabromo phthalic anhydride and 10 parts of arsenic trioxide having an average particle size between 1 and 2 microns were dispersed in 40 parts of water similarly to Example V. The resulting dispersion was designated X.

Using a standard pebble mill a latex exterior paint was prepared using the following formulations:

The dispersions were prepared by predissolving the ingredients in the given order in a tank equipped with a high-speed high-shear mixer and then transferring the resulting dispersion into the pebble mill and milling for 5 hours.

Two pieces of plywood were coated on both sides with dispersions X-A and X-B using a paint brush and air dried at room temperature.

The flammability of both pieces of plywood was tested by applying to them a flame from a butane blow torch for 15 seconds. The piece of plywood treated with dispersion X-A immediately extinguished after removal of the blow torch giving a charred surface where the flame was in contact with the coating, whereas the plywood coated with dispersion X-B continued burning until completely consumed.

70 parts of finely divided hexachlorocyclopentadienodibromocyclooctane and 10 parts of micropulverized antimony trioxide having a particle size between 1 and 2 microns were dispersed in 40 parts of water following procedure given in Example V. This dispersion was designated dispersion XI.

20 Parts of dispersion XI were dispersed in 40 parts of water and 40 parts of a 50% aqueous emulsion of a polymer obtained by reaction of a mixture of isomers of toluene diisocyanate and a condensation product of ethylene glycol having a molecular weight of approximately 4,000 and a hydroxyl of Example VI.

A piece of 100% nylon upholstery fabric was immersed in this solution and excess removed by squeezing between two rollers to achieve a 70% wet pickup and then dried at 125.degree. C.

The fabric thus treated was judged flame retardant when it gave a 3" char length when listed according to AATCC method 34-1969, whereas the untreated fabric burned the entire length when tested according to the same method.

Using the techniques and formulations of any of the examples given, namely I through XI, the following compounds may be used for application to the various bases identified in the several examples:

Polybrominated biphenyl=hexabromo

Polybrominated biphenyl oxide=decabromo biphenoloxide

Polybrominated benzene=hexabromo

Polybrominated toluene=pentabromo toluene

Polybrominated chlorotoluene=tetrabromine

Polybrominated phenol=pentabromo phenol

Polybrominated aniline=tribromo aniline

Polybrominated benzoic acid=dibromo benzoic acid

Tris phosphates of polybrominated phenols

Polybrominated cyclopentane=tetrabromo cyclo

Polybrominated cyclophexane=hexabromo cyclo

Polybrominated cyclooctane=hexabromo cyclo

Polybrominated cyclodecane=hexabromo cyclo

Polybrominated cyclododecane=hexabromo cyclo

Hexachlorocyclopentadieno-dibromocyclooctane=hexabromo cyclo

N,N'-ethyl-bis(dibromo-norbornene-dicarboximide)=hexabromo cyclo

Per chloro penta cyclodecane

The matter of flammability of a material and particularly the flammability of a fabric is something which is purely relative. Virtually any organic compound because it is composed of carbon-hydrogen-oxygen atoms will burn if conditions are right. As a matter of public safety those materials which go into general circulation and general public use which have high natural flammability are currently the subject matter of rather close regulation. The regulations stem from statutory authority given to the Department of Commerce which has issued regulations defining flammability, principally of fabrics. In all of the examples of this specification and the use of the variety of compounds mentioned, the basic problem is to attain a level of flame retardance in material treated which will at least meet the standards established by the Department of Commerce under its statutory authority. Thus, these regulations are summarized as folows:

Department of Commerce Fabric Flammability 3-71 (DOC-FF) Public Law No. 88, 1953, 83rd Congress, amended 1956, sets up standards for flame retardancy.

Public Law 90, 90th Congress, Department of Commerce regulations set up standards of flammability.

Department of Commerce Fabric Flammability 1-70, Federal Register 35, 74, Apr. 16, 1970, sets up standard for carpets and rugs; expanded Dec. 29, 1970, Federal Register 35, 251, small carpets and rugs, Dec. 29, 1970.

Department of Commerce Fabric Flammability 3-71; Children's Sleepware standard for flammability; Federal Register 36, 146, July 29, 1971.

Department of Commerce Fabric Flammability 4-72, sets up standards for mattresses.

Department of Transportation-Automotive Safety standard No. 302 deals with flammability of interior materials for cars.

The Federal Hazardous Substances Act also establishes certain standards of flammability but these standards are within the scope of the tests outlined. In other words it would appear that as a practical matter of operativeness the flammability of a material if it is to be considered nonflammable should be equivalent to that required under the regulations.

In summary and as a possible reference point I have tabulated in the following the identity of the product, the agency whose regulations apply and the nature of tests, etc., which is established by its authority.