NON-BLOOMING, STABILIZED FLAME RETARDANT
COMPOSITIONS AND METHOD OF FLAME
RETARDING POLYOLEFINS
BACKGROUND OF THE INVENTION
Field Of The Invention:
The present invention is directed to stabilized flame retardant compositions for polymers, preferably polyolefms, and methods of flame retarding polymers, particularly aliphatic polyolefms, by adding thereto a combination of flame retardant compounds (a) and (b) wherein (a) is an aromatic oligomeric compound, preferably having a weight average molecular weight of at least 2,000 and including aromatic bromine, (b) is a monomer ic or dimeric aromatic compound, preferably having a molecular weight less than 2,000 and including aliphatic bromine, wherein the weight ratio of (a):(b) is in the range of about 1 : 10 to 10: 1, preferably at least 1 : 1, more preferably at least 1.1:1, most preferably at least 1.3: 1. Optionally , the composition also contains (c) an antioxidant process stabilizer; and (d) a UV degradation retardant selected from the group consisting of an ultraviolet (UV) stabilizer; a UV absorber; a UV screener; and a combination of any two or more of said UV degradation retarders. This combination of flame retardants, antioxidant process stabilizer and UV degradation retardant(s) shows low surface migration (bloom) characteristics in polymers, particularly aliphatic (non-aromatic) polyolefms; and good retention of physical properties and/or color in polyolefm fibers and films, particularly for polyethylene, polypropylene and copolymers thereof.
Background Of The Invention And Prior Art:
It is known that halogen-containing compounds, together with antimony oxide, are frequently utilized with polymers, to impart flame retardant properties to the polymers. Commercially available halogenated flame - retardants that have a high melting point tend to contain large amounts of aromatic halogens or are polymeric. These molecules tend to be inefficient flame retardants for polyolefms. Lower molecular weight halogen compounds that are efficient flame retardants and that contain aliphatic bromine tend to undergo surface migration in polyolefms. This leads to marring of the surface appearance of the polyolefm.
It is also known to add one or more antioxidant process stabilizers during the manufacture of polyolefms to prevent oxidation of olefins during the polymerization reaction, and to add one or more antioxidants to a polyolefm during processing, e.g., during fiber formation, to prevent oxidation of the polyolefm.
Commercially available halogenated flame retardants also are generally reactive with UV light in polyolefms, e.g., polypropylene, causing degradation of the polyolefm, as demonstrated by decreasing tensile strength of the polyolefm-containing polymer composition. The addition of one or more UV degradation retardants decreases the degradation rate.
GPP-39®, a trademark of Great Lakes Chemical Corporation, is a graft copolymer of polypropylene with brominated polystyrene. It was developed as a flame retardant for polypropylene fiber. Attempts to UV stabilize the GPP-39 in polypropylene gave results similar to unstabilized
polypropylene - the polypropylene degradation rate was still too high for use of the GPP-39 flame retardant in polypropylene fiber applications.
This invention, accordingly, is directed to improvements in stabilized flame retarded polymer compositions, and in particular polyolefm compositions, more particularly, toward flame retarded and UV stabilized polyolefm fiber compositions, where there is a tendency for the flame retardant to bloom and a great tendency to degrade under exposure to UV light, and is directed towards inhibiting this bloom and degradation.
U.S. Patent No. 3,730,929 teaches that the use of a fatty acid or a metal salt of a fatty acid minimizes the tendency toward exudation. Dispersants have been disclosed to reduce blooming in U.S. Patent No. 4,006, 118.
U.S. Patent No. 4,699,734 discloses that an epoxy resin, e.g. , Epon 1031 , an epoxy having an epoxy equivalent of about 220, an elastomer ic resin, e.g. , a styrene-butadiene-styrene block copolymer, and a nucleating agent, such as a fire -dried fumed silica gel, are needed to minimize surface migration of the flame retardant in polypropylene. When any one or more of the ingredients were omitted, then the surface appearance was poor to fair after aging.
WO 98/17718 discloses the use of aliphatic-containing bromine molecules as synergists for tris(tribromoneopentyl) phosphate in polyolefm resins. Tris(tribromoneopentyl) phosphate may act as a bloom suppressant for PE-68 and Nonen-52.
U.S. Patent No. 5,559, 172 discloses the use of an oligomer based on tetrabromobisphenol A, ethylene dibromide, and end-capped with methyl bromide as a flame retardant for vinyl aromatic resins, such as ABS and HIPS, and blends with polycarbonate and polyphenylene oxide. The oligomer is disclosed to exhibit good thermal color stability and no bloom in these polymer compositions. U.S. Patent No. 5,530,044 discloses a composition of an oligomer material where the end group is an unreactive alkyl group. Neither patent discloses that the oligomeric flame retardant is an effective flame retardant for polyolefms, nor does either patent disclose reduced exudation in polyolefms .
Hei 5-320439 discloses that tetrabromobisphenol S bis(2,3- dibromopropyl) ether in combination with brominated bisphenol A carbonate oligomers, or with brominated bisphenol ethyl ether oligomer s, gave less surface exudation than tetrabromobisphenol S bis(2,3-dibromopropyl) ether used alone in polypropylene. The tetrabromobisphenol S bis(2,3- dibromopropyl) ether monomer to oligomer weight ratio is 99: 1 to 1 : 1 , with the range of 19: 1 to 3:2 being preferred.
Japanese Patent Application Kokai Sho 54-106557 discloses the use of a combination of tetrabromobisphenol A bis(2,3-dibromopropyl) ether and brominated bisphenol A carbonate oligomers as a low bloom, efficient flame retardant combination for polypropylene. The preferred weight ratio range of ether to carbonate flame retardants is 9: 1 to 1: 1. Ratios of less than 1 : 1 are not disclosed as being useful, and many of the oligomeric species tested had a weight average molecular weight below 2,000.
Japanese Patent Application Kokai Hei 8-59902 discloses the use of brominated epoxy resins as bloom inhibitors for tetrabromobisphenol A bis(2,3-dibromopropyl) ether. The weight ratio range of epoxy to tetrabromobisphenol A bis(2,3-dibromoρropyl) ether is 1: 1 to 1:2. An attempt to use bisphenol A carbonate oligomers or brominated bisphenol ethyl ether oligomers gave either poor flammability performance, high bleeding or both.
Japanese Patent Application Kokai Sho 57-192443 discloses a flame retardant composition obtained by combining polypropylene with a mixture comprising a brominated bisphenol A ethyl ether oligomer with a mixture of tetrabromobisphenol A bis(2,3-dibromopropyl) ether and tetrabromobisphenol S bis(2,3-dibromopropyl) ether and/or tris (2,3- dibromopropyl) isocyanurate. As stated in this published application, low bleeding and high flame retarding could not be achieved with only the oligomeric compound (a) and monomeric/dimeric compound (b); thus, at least a three component mixture is disclosed to be needed for acceptable flame retardancy and bloom characteristics since the higher molecular weight oligomer of the present invention and the correct weight ratios, were not utilized.
Japanese Patent Application Hei 4-309542 discloses a flame- retardant resin composition formed by compounding 100 parts by weight polyolefin resin with 5-50 parts by weight organic halogen flame retardant having a bromoalkyl group in its structure, antimony trioxide at 3/1 - 1/6 antimony /halogen in the organic halogen flame retardant (molar ratio), 0.05-2.0 parts by weight alicyclic aliphatic epoxy compound, and 0.1 - 10.0 parts by weight pentaerythritol and/or pentaerythritol oligomer.
There is still a need for a simple flame retardant/UV stabilizer composition that exhibits good flame retardant performance with low surface exudation, and reduced polymer degradation in polymer compositions, particularly polyolefms, when the polymer containing the flame retardant/stabilizer combination is exposed to UV light.
SUMMARY OF THE INVENTION
The present invention is directed to a unique blend of brominated flame retardants. Preferably, the composition also contains an antioxidant process stabilizer, and UV degradation retardant(s) combination including one or more UV degradation retardants selected from a UV stabilizer, a UV absorber, a UV blocker or screener, and any combination thereof that exhibits low surface migration (surface bleeding) even under accelerated oven testing while mamtaimng good flame retardancy despite the fact that one of the flame retardant components may show exudation when used by itself. The brominated flame retardant composition includes two or more flame retardant components, and must contain at least one oligomeric flame retardant. The oligomeric flame retardant component (component (a)) should contain aromatic bromine or a combination of aromatic bromine and aliphatic bromine while the monomeric or dimeric flame retardant component (component (b)) contains aliphatic bromine, and may contain a mixture of aliphatic bromine and aromatic bromine. Furthermore, the oligomeric flame retardant component should be compatible with the monomeric or dimeric flame retardant component, and should have a weight average molecular weight (Mw) of at least 2,000, as measured by GPC (Gel Permeation Chromatography) . In addition, the weight ratio of the oligomeric flame retardant component (a) to the monomeric or dimeric flame retardant component (b) should be in the range of about 1 : 10 to
10: 1 , preferably at least 1 : 1 , more preferably at least 1.1 : 1 , most preferably at least 1.2: 1 and to achieve the full advantage of the present invention, at least 1.3: 1. If the ratio of component (a) to component (b) is too low, then good flame retardancy will be exhibited but the final composite will show bloom after 24 hours of accelerated aging. Conversely, if the ratio of component (a) to component (b) is too high, then the composite will show low surface migration but poor flammability performance.
In addition to the combination of brominated flame retardants, in accordance with the present invention, additional optional additives to the polymers, particularly polyolefins, include about 0.05% to about 2% , preferably about 0.1 % to about 1 % , based on the weight of the polymer, of an antioxidant acting as a process stabilizer, and about 0.1 % to about 3 % , preferably about 0.2% to about 2%, based on the weight of the polymer, of one or more UV degradation retardants selected from the group consisting of a UV stabilizer, a UV absorber, a UV blocker or screener, and any combination thereof. Typical antioxidant process stabilizers include aromatic phosphites, aliphatic phosphites, aromatic phosphonites, aliphatic phosphonites or combinations of these. Examples of UV degradation retarders include a hindered amine light stabilizer (HALS), UV absorber and/or a UV screener. Typical HALS include aliphatic hindered amines, dimeric hindered aliphatic amines, polymers containing the aliphatic amine in the backbone of the polymer or as a pendant group, or combinations of different HALS. The amine may be secondary or ternary and may be either a liquid or a solid. UV absorbers include alkoxy- or hydroxy-substituted benzophenones or hydroxyphenyl or substituted hydroxyphenyl benzotriazoles. UV screeners may consist of inorganic or organic pigments, metal oxides such as titanium dioxide and carbon black. Substituted phenols, especially hindered phenols and
isocyanurate substituted cresols, may be used as antioxidants. The stabilizer package may also contain acid scavengers such as metal salts of carboxylic acids and other basic or alkaline materials.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
For the purpose of promoting an understanding of the principles of the invention, reference will now be made to preferred embodiments and specific language will be used to describe the same. It will nevertheless be understood that no limitation of the scope of the invention is thereby intended, such alterations and further modifications in the illustrated embodiments, and such further applications of the principles of the invention as illustrated herein being contemplated as would normally occur to one skilled in the art to which the invention pertains.
The present invention relates to a mixture of an oligomeric flame retardant component (a), preferably having a weight average molecular weight of at least 2,000, with a non-oligomeric (monomeric or dimeric) flame retardant component (b), preferably having a weight average molecular weight of less than 2,000. Preferably, a polymer stabilizer combination also is included in the composition comprising (c) an antioxidant process stabilizer and (d) a UV degradation retardant selected from the group consisting of (i) a UV stabilizer, (ii) a UV absorber, (iii) a UV blocker or UV screener; and (iv) any combination of two or more of the foregoing UV degradation retardants. In paπicular, the oligomeric flame retardant component (a) can be represented by the following formula I:
(I) where G is a connecting group selected from the group consisting of a single bond, a branched or unbranched divalent aliphatic radical of from 1 to 10 carbons, oxygen, sulfur, sulfoxide, sulfone, or oxygen-silicon; x is an integer from 1-4; and R and R' are each (same or different) a branched or unbranched alkyl radical, A is a branched or unbranched alkyl diradical; and n is a positive integer greater or equal to 2.
In certain embodiments, G is a connecting group of the formula -CYY' where Y and Y' (same or different) are each an aliphatic hydrocarbon radical and, in particular, methyl radicals. In other preferred embodiments, G is an SO2 connecting group.
In other embodiments, A may be CH2CH2. In the preferred embodiment, G is a C(CH3)2 connecting group; and A is a CH H connecting group, R and R' are CH2CH2Br groups.
Alternatively, or in addition, the oligomeric flame retardant component (a) may consist of a bromine-containing epoxy oligomer with a weight average molecular weight of 1 ,000-50,000 of the following formula (II):
(ID where G is a connecting group selected from the group consisting of a single bond, a branched or unbranched divalent aliphatic radical of from 1 to 10 carbons, oxygen, sulfur, sulfoxide, sulfone, or oxygen-silicon, X is an integer from 1-4, and R" and R"' are, independently, a branched or unbranched alkyl epoxy radical, branched or unbranched alkyl alcohol radical, branched or unbranched alkyl ether radical or branched or unbranched alkylhalide alcohol radical; C is a branched or unbranched alkyl diradical containing a hydroxy or ether group and n is a positive integer greater than or equal to 2.
In the preferred embodiment for formula II, G' is a (CH3)2C group, C is a CH2CHOHCH2 group, R"' is
JCL
H2C CH CH2
x is 2 and n is greater than 2.
The second, monomeric or dimeric flame retardant component (b) comprises a material having the following formula III:
(HI)
where G" is a connecting group selected from the group consisting of a single bond, a branched or unbranched divalent aliphatic radical of from 1 to 10 carbon atoms, oxygen, sulfur, sulfoxide, sulfone, or oxygen-silicon; x" is an integer from 0-4; and R"" and R'"" (same or different) each is selected from a branched or unbranched alkyl radical, branched or unbranched alkyl halide radical, and wherein at least of one R"" and R"'" contains bromine; A' is a branched or unbranched alkyl diradical or halogenated dialkyl radical; and n is a positive integer of 0 or 1.
In certain embodiments, G" is a connecting group of the formula
-CYY', where Y and Y' (same or different) each is an aliphatic hydrocarbon radical and, in particular, methyl radicals. In other embodiments, G" is an SO2 connecting group. In other embodiments, R"" and R""' are 2,3-dibromopropyl groups.
In the preferred embodiment, G" is a C(CH3)2 connecting group; n is 0; and both R"" and R""' are CH2CH2BrCH2Br groups. In a separate
embodiment, G" is an SO2 connecting group; n=0; and both R"" and R""' are 2,3-dibromopropyl groups.
The second, monomeric or dimeric flame retardant component (b) may also be selected from the following flame retardants: ethylene bis(5,6-dibromonorborane-2, 3-dicarboximide); hexabromocyclododecane; the Diels-Alder adduct of hexachlorocyclopentadiene with 1,5-cyclooctadiene; and tris(tribromoneopentyl)phosphate; bis(2,3-dibromopropyl)tetrabromophthalate, and the like.
The optional stabilizer package should contain an antioxidant, acting as a process stabilizer, and one or more UV degradation retardants.
Typical process stabilizers contain aromatic phosphites, aliphatic phosphites, aromatic phosphonites, aliphatic phosphonites, benzufuran(2) ones, especially
3-arylbenzofuranones, hydroxyl amines, or any combinations of these.
Examples are tris(2,4-di-tert-butyl-phenyl) phosphite, also known as Alkanox® 240 (Alknox® is a trademark of Great Lakes Chemical Corporation) or
Irgafos® 168 (Irgafos® is a trademark of Ciba Specialty Chemicals); bis(2,4-di- tert-butyl-phenyl)pentaerythritol diphosphite, also called Alkanox® P-24 or
Ultranox® 626 (Ultranox® is a trademark of General Electric Corporation); tetrakis (2,4-di-tert-butyl-phenyl)4,4'-biphenylene-diphosphonite, also known as Alkanox® 24-44 or Irgafos® P-EPQ; bis(2,4-dicumylphenyl)pentaerythritol diphosphite, also called Alkonox® 28 or Doverphos® S-9228 (Doverphos® is a registered trademark of Dover Corporation); and tris(p-nonyl- phenyl)phosphite, also called Alkanox® TNPP or Doverphos® 4-HR.
Substituted phenols, especially hindered phenols and isocyanurate substituted methylene phenols, may be used as antioxidant process
stabilizers. Specific examples of such antioxidants are 2-(2'-hydroxy-3',5'-di- tert-butylbenzyl)isocyanurate, also known as Anox™ 1C-14 (Anox™ is a trademark of Great Lakes Chemical Corporation) or IRGANOX® 3114, a trademark of CIBA Specialty Chemicals; tetrakismethylene (3,5-di-t-butyl-4- hydroxyhydrocinnamate)methane, also called Anox™ 20 or IRGANOX® 1010; octadecyl 3-(3',5'-di-t-butyl-4'-hydroxyphenyl)propionate, also called Anox™ PP18 or IRGANOX® 1076; and l,3,5-tris(2,6-dimethyl-3-hydroxy-4-tert- butylbenzyl)isocyanurate, also called Cyanox® 1790. (Cyanox® is a registered trademark of Cytec Corporation).
The stabilizer package preferably also contains at least one of a
UV degradation retarder or UV stabilizer such as a hindered amine light stabilizer (HALS), UV absorber or a UV screener. Typical HALS include aliphatic hindered amines; dimeric hindered aliphatic amines; polymers containing the aliphatic amine in the backbone of the polymer or as a pendant group; or combinations of different HALS, and hydroxyl amines. The amine may be secondary or ternary and may be either a liquid or a solid. Specific examples of HALS include bis-(l,2,2,6,6-pentamethyl-4-piperidinyl)-sebacate, also known as Lowlite® 76 (Lowlite® is a trademark of Great Lakes Chemical Corporation) or Tinuvin® 765 (Tinuvin® is a trademark of Ciba Specialty Chemicals) or Tinuvin® 292; bis-(2,2,6,6-tetramethyl-4-piperidinyl)-sebacate, also called Lowlite® 77 or Tinuvin 770®; butanedioic acid, dimethyl ester, polymer with 4-hydroxy-2,2,6,6-tetramethyl-l-piperidineethanol, also called Lowlite® 62 or Tinuvin® 622; poly-methylpropyl-3-oxy-[4(2, 2,6,6- tetramefhyl)piperdinyl] siloxane, also called Uvasil® 299 (Uvasil® is a trademark of Great Lakes Chemical Corporation); poly-methylpropyl-3-oxy- [4(l,2,2,6,6-pentamethyl)piperdinyl] siloxane, also called Uvasil® 816; decanedioic acid, bis[2,2,6,6-tetramethyl-l-(octyloxy)-4-piperidinyl] ester, also
called Tinuvin® 123; (poly[[6-[l , l ,3,3-tetramethylbuty)amino]-l,3,5-triazine- 2, 4-diyl] [(2,2,6, 6-tetramethyl-4-piperidinyl)imino]-l ,6-hexanediyl[2, 2,66- tetramethyl-4-piperidinyl)imino]] , also called Chimassorb® 944 (Chimassorb® is a trademark of Ciba Specialty Chemicals), also known as Lowlite® 94; 1-piperidineethanol, 4-hydroxy-2,2,6,6-tetramefhyl-, polymer with butanedioic acid, called Tinuvin® 622, Tinuvin® 111, l,3,5-triazine-2,4,6-triamine; N,N"'- 1 , 2-ethanediylbis [N-[3-[[4 , 6-bis [buty 1( 1 , 2 ,2 , 6 , 6-pentamethyl-4- piper idinyl)amino]- 1 , 3 , 5-triazin-2-y l]methy laminojpropy 1] -N' ,N"-dibuty 1-N' , N"- bis(l,2,2,6,6-pentamethyl-4-piperidinyl), also known as Chimassorb® 119; 3- dodecyl-N-(2,2,6,6-tetramethyl-4-piperidinyl)succinimide, also called Cyasorb® UV 3604 (Cyasorb® is a trademark of Cytec Corporation); 3-dodecyl-N- (2,2,6,6-tetramefhyl-4-piperidinyl)succinimide, also called Cyasorb® UV3581; poly [[6-(4-morpholinyl)- 1 ,3, 5-triazine-2, 4-diyl] [(2,2,6, 6-tetramethyl-4- piperidmyl)imino]-l ,6-hexanediy] [(2.2,6,6-tetramethyl-4-piperidinyl)imino]] , also called Cyasorb UV 3346; and 7-oxa-3,20- diazadispiro[5, l , l l ,2]heneicosan-21-one. 2,2,4,4-tetramethyl-20-
(oxiranylmethyl)-, homopolymer, also known as Hostavin® N 30 (Hostavin® is a registered trademark of Clariant Corporation). Specific examples of mixed HALS containing systems are Chimasorb® 111 , a blend of Tinuvin® 622 and Chimasorb® 119, and FS 410® a blend of Chimasorb® 944 and di(octadecyl)hydroxyl amine.
UV absorbers include alkoxy or hydroxy substituted benzophenones or hydroxyphenyl or substituted hydroxyphenyl benzotriazoles. Specific examples of UV absorbers are 2,4-dihydroxybenzophenone, 2-hydroxy-4-n-octoxy-benzophenone, also called Lowlite® 22 or Chimassorb® 81; 2-(2'-hydroxy-3',5'-ditert-butyl-phenyl)-5-chlorobenzotriazole, also known as Lowlite® 27 or Tinuvin® 327; 2-(2'-hydroxy-3'-tert-butyl-5'-methyl-phenyl)-
5-chlorobenzotriazole, also called Lowlite® 26 or Tinuvin® 326; 2-(2'-hydroxy- 3',5'-di-t-amylphenyl)benzotriazole, also called Lowlite ® 28 or Tinuvin® 328; and 2-(2'-hydroxy-5'-methyl-phenyl)benzotriazole, called Lowlite® 55 or Tinuvin® P. UV screeners may consist of inorganic or organic pigments, metal oxides such as titanium dioxide, and carbon black.
The stabilizer package may also contain acid scavengers such as metal salts of carboxylic acids. Typical examples include calcium stearate, zinc stearate, calcium lactate, aluminum-magnesium hydrotalcite and other basic or alkaline materials. Optionally, the stabilizer package, when added to the fibrous or non-fibrous polymer, may include a flame retardant synergist in an amount in a ratio of flame retardant: flame retardant synergist in the range of about 10: 1 to 3: 1 , preferably in the range of about 2-6: 1. Examples of flame retardant synergists include antimony trioxide, zinc borate, and sodium antimonate.
The combination of the flame retardant components, optional antioxidant process stabilizer and optionally one or more UV degradation retarders are useful as flame retardants, particularly when compounded with other plastic compounds or polymer compositions, particularly polyolefms, preferably aliphatic polyolefms, such as polyethylene and polypropylene and copolymers thereof. The combination of flame retardant compounds of the present invention is less prone to surface migration, while maintaining good flame retardancy. The preferred addition of the antioxidant process stabilizer and one or more UV degradation retarders prevents the degradation of physical properties and/or color in the polymer, particularly in polyolefin fibers and film, particularly polypropylene.
The combination of flame retardants of the present invention is useful as a stabilized flame retardant in polymeric materials such as polystyrene; high impact polystyrene; copolymers of styrene; polycarbonates; polyurethanes; polyi ides; polyamides; polyethers; acrylics; polyesters; epoxies; phenolics; elastomers, such as butadiene/styrene copolymers and butadiene/acrylonitrile copolymers; te olymers of acrylonitrile, butadiene and styrene; natural rubber; butyl rubber; polysiloxanes, and particularly polyolefins, including fibers made from any of the foregoing. Preferred polymers (particularly fiber or film) include those of olefinically-saturated monomers, such as ethylene, propylene, butene, butadiene and copolymers of two or more of such alkylene monomers. Blends of polymers may also be flame retarded and stabilized with the combination of flame retardants and stabilizers/UV degradation retardants disclosed herein.
The most preferred polymers are aliphatic polyolefins, particularly polyethylene, polypropylene, and copolymers of propylene and ethylene, preferably where the polyolefm and polyolefm copolymers are in fiber form.
The oligomeric flame retardant component (a) of the present invention may be prepared by reacting a diphenol with a divalent reactant, for example carbonyl dichloride, in the presence of a base, in a solvent such as methylene chloride. A second phenol can be added to end cap the oligomer.
The flame retarded polymer compositions of the present invention may be prepared by mixing the oligomeric flame retardant component
(a), the monomeric or dimeric flame retardant component (b), preferably also the optional antioxidant process stabilizer (c), and the optional UV degradation
retarder (d) with the polymer to be flame retarded, e.g. , at the same time. However, a premixing of the flame retardant components (a) and (b) with the optional process stabilizer component (c) and the optional UV degradation retarder(s) (d) is preferred. The flame retardant components (a) and (b) , the optional stabilizer component (c), and the optional UV degradation retarder(s) (d) may be blended by mixing the powders; melting the components and then mixing; or one component may be melted or softened and the components then mixed. Typical mixing apparatus includes, but is not limited to, high shear mixers, such as a Banbury mixer; tumble type blenders; and extruders. It is further preferred to mix the components (a) and (b) with the optional stabilizer and UV degradation retarder(s) (c) and (d) and then blend the complete package with the polymer. The flame retardant stabilized mixtures of the present invention may be used as a fine powder, as a compacted material, or may be used with a small amount of a suitable binder as a master batch. Suitable binders include, but are not limited to, calcium stearate, antimony trioxide, polyethylene, polypropylene, propylene/ethylene copolymers, and poly(brominated styrene). Suitable forms of the compounds of this invention include powder, compacted, prilled, chilsinated, and the like.
The compositions of this invention, when including components (c) and (d), may also be added in a stepwise manner. For example, the antioxidant process stabilizer component (c) can be added to the polyolefm followed by addition of the flame retardant components (a) and (b) and then a UV degradation retardant (d), such as HALS; or followed by the flame retardant components (a) and (b) and then a UV degradation retarder, e.g. , HALS, and then an acid scavenger. One skilled in the art can envision multiple methods of sequencing the addition of the ingredients of the composition of this invention.
Optionally, the flame retardant combination, when added to the fibrous or non- fibrous polymer, preferably a polyolefm used to make a polyolefm in fiber or film form, may include a flame retardant synergist in an amount in a weight ratio of flame retardant: flame retardant synergist in the range of about 10: 1 to 3: 1 , preferably in the range of about 2-6: 1. Examples of flame retardant synergists include antimony trioxide, zinc borate, and sodium antimonate.
Reference will now be made to specific examples of combinations of flame retardant components (a) and (b), described above. It is to be understood that the examples are provided to more completely describe preferred embodiments, and that no limitation of the scope of the invention is intended thereby.
General Experimental Procedure:
The oligomeric component (a), monomeric or dimeric component (b), antimony trioxide (5: 1 weight ratio of total flame retardant to antimony trioxide), are weighed into the polyolefm and the mixture is thoroughly hand mixed in a poly bag. Alternatively, the oligomeric component (a) and monomeric or dimeric component (b) are mixed in a ribbon blender and then weighed, with antimony oxide, into the polyolefm and then thoroughly mixed. The material is compounded on a Berstorff ZE-25 twin screw extruder at the conditions shown below (see Table 1).
TABLE 1
Compounding Conditions On Berstorff ZE-25 Twin Screw Extruder
Barrel 2 Temperature (°C) 195 Screw Speed (rpm) 200
Barrel 3 Temperature (°C) 200 Barrel 4 Temperature (°C) 200 Feeder Belt
Barrel 5 Temperature (°C) 200 Feed Rate (g/min) 150-200
Barrel 6 Temperature (°C) 200
Barrel 7 Temperature (°C) 200 Typical Melt Temperature (°C) 220
Die Temperature (°C) 205 Typical Melt Pressure (psi) 350-450
A belt feeder was used to feed the formulation mixture to the throat (i.e. , barrel 1) of the twin screw. The throat was cooled to 80-90°F. The formulation strands were cooled in a 6 foot water bath (Ca. 75-80°F), then air dried and pelletized using a Conair/Jetro Model #304 pelletizer.
Experimental For Molding Bloom Plaques On A Boy 50 Ton:
Bloom plaques (Gardner impact plaques) and 1/16th inch UL-94 bars were molded on a Boy 50 Ton injection molder (Model #159-50 at the conditions shown below (See Table 2).
TABLE 2
Bloom Plaque And l/16 h Inch UL-94 Bar Molding On A Boy 50 Ton
Barrel 1 Temperature (°C) 200 Injection Time (sec) 10
Barrel 2 Temperature (°C) 200 Cooling Time (sec) 30 Barrel 3 Temperature (°C) 200
Nozzle Temperature (°C) 225 Typical Melt Temperature (°F) 440-450
Mold Temperature (°F) 90 Typical Inject Pressure (psi) 450-475
Bloom plaques and UL-94 bars were conditioned at 70-75 °F for 24 hours prior to start of testing.
Experimental For Accelerated Aging (Bloom) Test @ 80 °C (24 and 168 hours):
Two sets of 3 Bloom plaques per formulation were placed in wire mesh racks and conditioned in a circulating/vented oven at 80 °C for 24 and 168 hours. Each set was allowed to condition an additional 24 hours at 70-75 °F prior to performing the bloom test.
Visual haze was recorded. A 2.5" x 2.5" black cloth (broad cloth, 65% polyester/35 % cotton blend) was used to swipe the surface of the plaques.
EXAMPLES OF BLOOM SUPPRESSION WHILE MAINTAINING V-O OR V-2 FLAME RATING
Example Flame Retardant Component Bloom UL-94 (phr) Rating
A B C 24 hr 168 hr
1 11 medium to heavy medium to heavy V-O
2 3 medium to heavy medium to heavy V-2
3 24 very slight very slight fail
4 30.8 none none V-l
5 6 1 medium to heavy medium to heavy V-O
6 12.3 15.5 medium to heavy medium to heavy V-O
7 6.4 23.2 none none V-O
8 4 8 none none V-O
EXAMPLES OF BLOOM SUPPRESSION WHILE MAINTAINING V-O OR V-2 FLAME RATING
ample Flame Retardant Component Bloom UL-94 (phr) Rating
A B C 24 hr 168 hr
9D 7.3 3.7 light to medium medium V-O
10": 7.6 3.8 light V-O
1 1F 7.8 3.9 no bloom very light V-2
A = tetrabromobisphenol A bis(2,3-dibromopropyl ether) B = methyl end-capped tetrabromobisphenol A/ethylene dibromide oligomer (Mw < 2,000) C = methyl end-capped tetrabromobisphenol A/ethylene dibromide oligomer (Mw > 2,000) D = molecular weight 1100, mixture of CH2CH2Br and H end groups* E = molecular weight 2340, mixture of CH2CH2Br and CH3 end groups F = molecular weight 6110, CH2CH2Br end groups
* See JP 4849832
The above table demonstrates that the low molecular weight component blooms by itself even at low loadings (Examples 1 and 2). Furthermore, the oligomeric flame retardant, while showing low bloom characteristics, is an inefficient flame retardant (Examples 3 and 4). The combination of the two components gave compositions exhibiting excellent flame retardancy. However, high loadings of the monomeric component compared to the oligomeric component shows excellent flame retardancy but unacceptable surface exudation (Examples 5 and 6). Compositions were the ratio of oligomeric to monomeric flame retardant is above 1 : 1 show both good flame retardancy and low surface exudation (Examples 7 and 8).
Numerous modifications and alternative embodiments of the invention will be apparent to those skilled in the art in view of the foregoing description. Accordingly, this description is to be construed as illustrative only and is for the purpose of teaching those skilled in the art the best mode of carrying out the invention. The details may be varied substantially without departing from the spirit of the invention, and the exclusive use of all modifications which come within the scope of the appended claims is reserved.