IL47037A

IL47037A - Fire retardant copolymers

Info

Publication number: IL47037A
Application number: IL47037A
Authority: IL
Original assignee: Stauffer Chemical Co
Priority date: 1974-06-10
Filing date: 1975-04-07
Publication date: 1977-12-30
Also published as: NL7505905A; GB1512404A; JPS512795A; BE830035A; IL47037A0; DE2524525A1; FR2273825A1

Description

47037/2 Plre retardant copolymers STAUPFSR CHEMICAL COMPANY FIRE RETARDANT COPOLYMERS Abstract of the Disclosure Fire retardant copolymers of: (1) a bis (hydrocarbyl) vinylphosphonate, (2) a monomer which contains one ethylenically unsaturated bond, and (3) acrylic or methacrylic acid are disclosed. These copolymers are useful in a variety of applications, including as coatings, and as additives for enhancing the fire retardancy of thermoplastics.

Technical Disclosure of the Invention Prior art attempts to form copolymers of various bis (hydrocarbyl) vinylphosphonate, such as bis (beta-chloroethyl) vinylphosphonate, with monomers containing ethylenic unsat-uration, e.g. vinyl chloride, methyl methacrylate , and the like, have not produced products which were substantially free of unreacted vinylphosphonate. Two examples of such prior art processes are described in U.S. Patent No. 3,726,839 to Jung II Jin and U.S. Patent No. 3,691,127 to Paul Kraft et al.

The present invention relates to a copolymer of such a vinylphosphonate with an ethylenically unsaturated monomer and either acrylic or methacrylic acid. This novel copolymer contains higher levels of polymerized vinylphosphonate than found in copolymers known to the prior art. The amount of vinyl phosphonate varies between about 5-85% by weight of the final composition, the weight of ethylenically unsaturated monomer varies between about 10-85% by weight and the amount of either acrylic or methacrylic acid varies between about 2-50%. Preferred amounts are about 20-75% vinylphosphonate, about 20-60% ethylenically unsaturated monomer and about 5-40% acrylic or methacrylic acid. Particularly preferred weight amounts for these components are about 35-50%, about 35-50% and about 5-20% about 15-40% by weight, the final product contains sufficient pendant carboxyl groups to render it water soluble when neutralized. This allows the copolymer to be solubilized in water for coating applications.

The type of bis (hydrocarbyl) vinylphosphonate intended to be used in forming the copolymer of the present invention has the structure: X 0 - OR ' CH„ = C - P OR wherein X is selected from the group consisting of hydrogen, halogen, cyano, aryl, such as phenyl, Ci-C18 alkyl and 0 wherein R and R1 are hydrocarbyl and substituted hydrocarbyl groups consisting essentially of hydrogen and carbon and containing up to about 18 carbon atoms inclusive with the proviso that R and R' may be the same, different or conjoint, i.e., R and R' may form one single radical.

The use, in this disclosure, of the expression, "hydrocarbyl" and "substituted hydrocarbyl" groups refers to the radicals obtained upon the removal of a hydrogen from a hydrocarbon or substituted hydrocarbon group which may be either an aliphatic or aromatic group. These hydrocarbyl groups may be substituted with any non-interfering groups, i.e, with any group which does not interfere with the polymerization of the bis- (hydrocarbyl) vinylphosphonate. Such substituent groups include, for example, chloro, bromo, fluoro, nitro, . C-3350 47037/2 Illustrative of such groups as are rep esented by R and R' are alkyl or alkenyl groups, such as methyl, ethyl, propyl, butyl, pentyl, hexyl, nonyl, pentenyl, and hexenyl groups and all of their respective isomers; cycloalkyl or cyclpalkenyl groups, such as cyclopropyl, cyclobutyl, cyclo-pentyl, cyclohexyl and cyclohexenyl groups and the like; while typical aryl groups represented by R and R" include phenyl, benzyl, phenethyl, tolyl and naphthyl groups and the like.

Representative of the above depicted bis (hydrocarbyl) vinyl phosphonates which may be used in preparing the fire re-tardant vinyl chloride copolymer latices of this invention are: Bis (beta-chloroethyl) vinylphosphonate; Bis (beta-chloropropyl) vinylphosphonate; Bis (beta-chloroethyl) 1-methylvinylphosphonate; Bis (beta-chloroethyl) 1-cyanovinylphosphonate; Bis (beta-chloroethyl) 1-chlorovinylphosphonate; Bis (beta-chloroethyl) 1-phenylvinylphosphonate; Dimethyl vinylphosphonate; Diethyl vinylphosphonate; Bis (omega-chlorobutyl) vinylphosphonate; Di-n-butyl vinylphosphonate; Di-isobutyl vinylphosphonate; Bis (2-chloroisopropyl) 1-methylvinylphosphonate; Diphenyl vinylphosphonate; and Bis (2 , 3-dibromopropyl) vinylphosphonate.

It is, however, to be emphasized that it is preferred to employ bis (beta-chloroethyl) vinylphosphonate in preparing the copolymer latices of this invention since the latter monomer is a commercially available material and lower in cost than any of the other above listed bis (hydrocarbyl) vinyl-phosphonates .

The types of monomers that contain one ethylenically unsaturated bond, i.e., vinyl compounds which copolymerize with the bis (hydrocarbyl) vinylphosphonate, form the second component of the copolymer of the present invention. Included with this class are: the vinyl halides such as vinyl chloride, vinyl bromide, vinyl fluoride and trifluoroethylene ; vinylidene halides such as vinylidene chloride, vinylidene bromide and vinylidene fluoride; alpha-olefins such as ethylene, propylene and butylene; vinyl esters of carboxylic acids such as vinyl acetate, vinyl butyrate, and vinyl stearate; the Ci-C2o alkyl esters of acrylic and methacrylic acid such as methyl methacry-late, methyl acrylate, ethyl aerylate, butyl acrylate, 2-ethyl-hexyl acrylate and lauryl acrylate; aryl, halo- and nitro- substituted benzyl esters of acrylic and methacrylic acid such as benzyl acrylate and 2-chlorobenzyl acrylate; ethylenically unsaturated dicarboxylic acids, their anhydrides and their Ci-C2o mono- and dialkyl esters such as aconitic acid, fumaric acid, maleic acid, itaconic acid, citraconic acid, maleic anhydride, dibutyl fumarate and monoethyl maleate; amides of ethylenically unsaturated carboxylic acids such as acrylamide and methacrylamide ; vinyl aryl compounds such as styrene and alpha-methyl styrene; nitriles of ethylenically unsaturated carboxylic acids such as acrylonitrile and methacrylonitrile; and, Ci-C2o alkyl vinyl ethers such as methyl vinyl ether, ethyl vinyl ether and stearyl vinyl ether. Preferred for use as optional comonomers are the vinyl halides particularly vinyl chloride; and vinylidene halides, particularly vinylidene chloride; the vinyl aryl compounds particularly styrene and the lower alkyl esters of acrylic and methacrylic acids .

The copolymer latices of this invention may be prepared by means of free radical initiated emulsion polymerization processes well known to those skilled in the art. In these procedures, the various monomers and catalysts are emulsified, in water, by means of one or more surface-active emulsifiers whereupon the polymerization reaction is then initiated.

Suitable water soluble, free radical initiating catalysts for use in preparing the copolymer latices of this invention include sodium, potassium and ammonium persulfate and hydrogen peroxide or one may use a redox system such, for example, as a mixture of a persulfate with an alkali metal bisulfite, thiosulfate or hydrosulfite. These catalysts should be present in a concentration of from 0.1 to 5% by weight, of the total monomer charge. With respect to the emulsifier or surfactant, it is possible to utilize one or more anionic, cationic, or non-ionic emulsifiers such, for example, as the alkyl carboxylic acid salts; the alkyl sulfate, sulfonate, phosphate, or sulfosuccinate salts; the alkyl aryl ether alcohols, and the alkyl aryl polyether sulfate salts. The selected emulsifier or emulsifiers should be present in a total concentration of from about 0.3 to 8%, by weight, of the total monomer charge. In addition, a protective colloid such as polyvinyl alcohol, methyl cellulose or gelatin can also, if desired, be present in the recipe in a concentration of from about 0.05 to 5%, by weight, of the total monomer charge.

The actual polymerization reaction will ordinarily be conducted at a temperature of from about 30 to 80°C. for a period of from about 6 to 24 hours, depending upon such C-3350 resulting from this polymerization process will ordinarily have a resin solids content of from about 20 to 50%, by weight, wherein the particles range in size from about 0.02 to 2 microns .

It should also be noted that, if desired, the copolymers of this invention can alternatively be prepared _¾ri in the form of aqueous suspensions which contain from 0.01 to 5%, as based upon the total weight of the monomer mixture, of a suspension agent, such as gelatin, starch, hydroxy-methyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, carboxymethyl cellulose, talc, clay, polyvinyl alcohol and the like. As a catalyst for the polymerization, one may use from about 0.05 to 5%, as based on the total weight of the monomer mixture, of a monomer soluble azo or peroxide catalyst such, for example, as azobisisobutyronitrile , lauroyl peroxide, benzoyl peroxide, isopropylperoxy dicarbonate, t-butyl peroxypivalate and the like.

Polymerization may ordinarily be initiated by heating the system to a temperature in the range of from about 20° to 150°C. for a period of from about 5 to 24 hours with agitation being applied throughout the course of the reaction. The resulting product will comprise an aqueous suspension of the copolymers which will be in the form of particulate solids having a resin solids content in the range of from about 5 to 60%, by weight. These copolymer particles will have a particle size in the range of from about 2 to 500 microns with a range of from about 20 to 250 microns being preferred when these copolymers are to be used as additives for preparing flame retardant thermoplastic polymers .

C-3350 The following Examples further illustrate the invention : EXAMPLE 1 A latex according to the present invention was pre-pared by mixing 558 grams of water, 1.5 grams of sodium lauryl sulfate and 2.0 grams of Triton X-20O, a sodium sulfonate salt of an ethoxylated alkyl phenol anionic emulsifier sold by Rohm & Haas Co., Inc., in a 3-necked flask under nitrogen and heating the mixture to 80°C. Forty grams of a catalyst solution of ammonium persulfate (2% solution) was added. To the resulting solution was then added a monomer mixture comprising 60 grams of methyl methacrylate , 60 grams of bis (beta-chloroethyl) vinyl-phosphonate and 30 grams of methacrylic acid in a dropwise manner over a period of one hour while maintaining the tem-perature at 80°C. The reaction medium was then heated to 90°C. for 5 minutes with no refluxing acrylic monomer noted.

The medium was cooled and an essentially gum free latex was filtered therefrom.

The latex was neutralized to a pH of 7-9 with dilute ammonium hydroxide and was cast into a film. The dried film exhibited an LOI of 26 using the test procedure described by Fenimore and Martin in the November, 1966 issue of Modern Plastics EXAMPLE 2 The procedure used in Example 1 was repeated but no methacrylic acid was used in the monomer mixture. The latex that was obtained contained about 20-30% unreacted oil which gas chromatographic analysis showed to be unreacted bis (beta-chloroethyl) vinylphosphonate.

C-3350 EXAMPLE 3 Another latex was prepared as set forth in Example 1. The components added to the reaction mixture were: Component Amounts (In Grams) Water 200 Methylmethacrylate 35 Bis (beta-chloroethyl) vinylphosphonate 35 Methacrylic acid 5 Sodium lauryl sulfate 0.8 Triton X-200 1 Ammonium persulfate (2% sol.) 20 Sodium meta bisulfite 10 A stable latex was again obtained.

EXAMPLE 4 A water soluble copolymer was formed by adding the following components to an appropriate reaction vessel: Component Amounts (In Grams) Water 200 Bis (beta-chloroethyl) vinylphosphonate 40 vinyl chloride 40 Acrylic acid 20 Surfactant (10% Sipex UB) 15 Triton X-200 2.5 Ammonium bisulfite (2% solution) 70 C-3350 This reaction mixture was heated at 50°C. for 5 hours with agitation (at 20 rpm) and had a 26% solids content. After neutralization with ammonium hydroxide to a pH of 7.0 a clear, water soluble system was produced. When added to water and applied as a surface coating, a hard flame resistant coating was produced.

The copolymers of this invention are useful as fire retardant additives for the types of thermoplastics listed in U.S. Patent no. 3,726 839 to Jung II Jin, and as coatings that have fire retardant properties.

Claims

C-3350 WHAT IS CLAIMED IS:

1. A fire resistant copolymer of: (1) a bis (hydrocarbyl) vinylphosphonate having the formula: X 0 wherein X is selected from the group consisting of hydrogen halogen, cyano, aryl, Ci-C18 alkyl, alkenyl, cycloalkyl or cycloalkenyl , and 0 wherein R and R' are hydrocarbyl and substituted hydrocarbyl groups consisting essentially of hydrogen and carbon and containing up to about 18 carbon atoms inclusive with the proviso that R and R1 may be the same, different or conjoint; (2) a monomer which contains one ethylenically unsaturated bond and which is copolymerizable with the vinylphosphonate; and (3) a monomer selected from the group consisting of acrylic and methacrylic acid.

2. A copolymer as claimed in claim 1 comprising from about 5-85% by weight of the vinylphosphonate.

3. A copolymer as claimed in claim 1 comprising from about 20-75% by weight of the vinylphosphonate. C-3350

4. A copolymer as claimed in claim 1 comprising fromiv about 35-50% by weight of the vinylphosphonate.

5. A copolymer as cliamed in claim 1 comprising from about 10-85% by weight of the ethylenically unsaturated monomer.

6. A copolymer as claimed in claim 1 comprising from about 20-60% by weight of the ethylenically unsaturated compound

7. A copolymer as claimed in claim 1 comprising from about 35-50% by weight of the ethylenically unsaturated compound

8. A copolymer as claimed in claim 1 comprising from about 2 and 50% by weight of acrylic acid or methacrylic acid.

9. A copolymer as claimed in claim 1 comprising from about 5-40% acrylic or methacrylic acid.

10. A copolymer as claimed in claim 1 comprising from about 5-20% by weight of acrylic or methacrylic acid.

11. A copolymer as claimed in claim 1 wherein the vinylphosphonate is bis (beta-chloroethyl) vinylphosphonate.

12. A copolymer as claimed in claim 1 wherein the ethylenically unsaturated monomer is selected from the group consisting of the vinyl halides, the vinylidene halides, the alpha-olefins , the vinyl esters of carboxylic acids, the C!-C2o alkyl esters of acrylic or methacrylic acid, the aryl, halo- and nitro- substituted benzyl esters of acrylic and methacrylic acid, ethylenically unsaturated dicarboxylic acids, the amides of ethylenically unsaturated carboxylic acids, the vinyl aryl compounds, the nitriles of ethylenically unsaturated carboxylic acids, and the Ca-C2o alkyl vinyl ethers . C-3350

13. A copolymer as claimed in claim 12 wherein the ethylenically unsaturated monomer is methyl methacrylate.

14. A copolymer as claimed in claim 12 wherein the ethylenically unsaturated monomer is vinyl chloride.

15. A copolymer as claimed in claim 7 wherein the ethylenically unsaturated monomer is vinyl bromide.

16. A copolymer as claimed in claim 1 comprising about 35-50% by weight of vinylphosphonate, about 35-50% by weight of the ethylenically unsaturated monomer, and from about 5-20% by weight of acrylic or methacrylic acid.