U.S. patent application number 12/148188 was filed with the patent office on 2008-10-30 for flame retardant halogenated polymer compositions.
Invention is credited to James D. Siebecker, Larry D. Timberlake.
Application Number | 20080269416 12/148188 |
Document ID | / |
Family ID | 39887755 |
Filed Date | 2008-10-30 |
United States Patent
Application |
20080269416 |
Kind Code |
A1 |
Timberlake; Larry D. ; et
al. |
October 30, 2008 |
Flame retardant halogenated polymer compositions
Abstract
A halogenated aryl ether oligomer is formed by halogenation of
an aryl ether oligomer and is useful as a flame retardant for
flammable macromolecular materials. Typically, the halogenated aryl
ether oligomer comprises the following repeating monomeric units:
##STR00001## wherein R is hydrogen or alkyl, especially C.sub.1 to
C.sub.4 alkyl, Hal is halogen, m is at least 1, n is 0 to 3 and x
is at least 2.
Inventors: |
Timberlake; Larry D.; (West
Lafayette, IN) ; Siebecker; James D.; (West
Lafayette, IN) |
Correspondence
Address: |
Jaimes Sher;CHEMTURA CORPORATION
199 Benson Road
Middlebury
CT
06749
US
|
Family ID: |
39887755 |
Appl. No.: |
12/148188 |
Filed: |
April 16, 2008 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
60926374 |
Apr 25, 2007 |
|
|
|
Current U.S.
Class: |
525/132 ;
525/420; 525/437; 525/534; 528/212 |
Current CPC
Class: |
C08K 5/06 20130101; C09K
21/08 20130101; C08K 5/0066 20130101; C07C 43/29 20130101 |
Class at
Publication: |
525/132 ;
528/212; 525/420; 525/534; 525/437 |
International
Class: |
C08L 71/12 20060101
C08L071/12; C08L 67/00 20060101 C08L067/00 |
Claims
1. A halogenated aryl ether oligomer formed by halogenation of an
aryl ether oligomer.
2. The oligomer of claim 1, wherein the halogen content of the
halogenated aryl ether oligomer is in the range of about 50 to
about 83 wt % of the oligomer.
3. The oligomer of claim 1 and having an average of least 3 aryl
rings.
4. The oligomer of claim 1, wherein the halogen is bromine.
5. The oligomer of claim 1, wherein the aryl ether oligomer is
brominated, comprises at least 5 aryl rings and has a molecular
weight up to 1,000,000 Daltons.
6. The oligomer of claim 1, wherein the oligomer comprises the
following repeating monomeric units: ##STR00011## wherein R is
hydrogen or alkyl, especially C.sub.1 to C.sub.4 alkyl, Hal is
halogen, m is at least 1, n is 0 to 3 and x is at least 2.
7. The oligomer of claim 6, wherein x is 5 to 20.
8. The oligomer of claim 6, wherein Hal comprises bromine.
9. The oligomer of claim 6, wherein said halogenated aryl ether
oligomer also comprises end groups each independently comprising
alkyl, alkoxy, aryl, aryloxy, hydrogen, halogen and hydroxyl.
10. A flame retardant polymer composition comprising (a) a
flammable macromolecular material and (b) a halogenated aryl ether
oligomer flame retardant formed by halogenation of an aryl ether
oligomer.
11. The composition of claim 10, wherein the halogen content of the
halogenated aryl ether oligomer is in the range of about 50 to
about 83 wt % of the oligomer.
12. The composition of claim 10 and having an average of least 3
aryl rings.
13. The composition of claim 10, wherein the halogen is
bromine.
14. The composition of claim 10, wherein the aryl ether oligomer is
brominated, comprises at least 5 aryl rings and has a molecular
weight up to 1,000,000 Daltons.
15. A flame retardant polymer composition comprising (a) a
flammable macromolecular material and (b) a halogenated aryl ether
oligomer flame retardant formed by halogenation of an aryl ether
oligomer, wherein said halogenated aryl ether oligomer comprises
the following repeating monomeric units: ##STR00012## wherein R is
hydrogen or alkyl, especially C.sub.1 to C.sub.4 alkyl, Hal is
halogen, m is at least 1, n is 0 to 3 and x is at least 2.
16. The composition of claim 15, wherein x is 5 to 20.
17. The composition of claim 15, wherein Hal comprises bromine.
18. The composition of claim 15, wherein said halogenated aryl
ether oligomer also comprises end groups each independently
comprising alkyl, alkoxy, aryl, aryloxy, hydrogen, halogen and
hydroxyl.
19. The composition of claim 15, wherein the flammable
macromolecular material (a) is a thermoplastic polymer or a
thermosetting polymer.
20. The composition of claim 15, wherein the flammable
macromolecular material (a) is polystyrene and the amount of
halogenated aryl ether oligomer flame retardant in the composition
is between about 5 and about 25 wt %.
21. The composition of claim 16, wherein the flammable
macromolecular material (a) is polypropylene and the amount of
halogenated aryl ether oligomer flame retardant in the composition
is between about 20 and about 50 wt %.
22. The composition of claim 15, wherein the flammable
macromolecular material (a) is polyethylene and the amount of
halogenated aryl ether oligomer flame retardant in the composition
is between about 5 and about 35 wt %.
23. The composition of claim 15, wherein the flammable
macromolecular material (a) is a polyamide or polyester and the
amount of halogenated aryl ether oligomer flame retardant in the
composition is between about 5 and about 25 wt %.
24. A flame retardant polymer composition comprising (a) a
flammable macromolecular material and (b) a halogenated aryl ether
having the following formula: ##STR00013## wherein each R.sup.1 is
independently selected from hydrogen, hydroxy, halogen and alkyl,
wherein each R.sup.2 is independently selected from hydrogen,
hydroxy, halogen and alkyl, provided at least one R.sup.2 is
halogen, n is 5, m is 4, and x is from 1 to 10.
25. The composition of claim 24, wherein x is from 2 to 6.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application claims the benefit of the filing date of
U.S. Provisional Application No. 60/926,374 filed Apr. 25, 2007,
the entire contents of which are incorporated herein by
reference.
FIELD
[0002] This invention relates to flame retardant halogenated
polymer compositions.
BACKGROUND
[0003] Decabromodiphenyl oxide (deca) and decabromodiphenylethane
(deca-DPE) are commercially available materials widely used to
flame retard various polymer resin systems. The structure of these
materials is as follows:
##STR00002##
[0004] One of the advantages of using deca and deca-DPE in polymer
resins that are difficult to flame retard, such as high-impact
polystyrene (HIPS) and polyolefins, is that the materials have a
very high (82-83%) bromine content. This allows a lower load level
in the overall formulation, which in turn serves to minimize any
negative effects of the flame retardant on the mechanical
properties of the polymer.
[0005] Despite the commercial success of deca, there remains
significant interest in developing alternative halogenated flame
retardant materials that are equally or more efficient, not only
because of economic pressures but also because they may allow lower
flame retardant loadings, which in turn may impart improved
performance properties. Improved properties, such as non-blooming
formulations, or better mechanical properties can potentially be
met by producing polymeric or oligomeric flame retardant compounds.
These types of materials would become entangled in the base resin
polymer matrix, depending on the compatibility, and hence should
show fewer tendencies to bloom.
[0006] There are a number of commercially available flame retardant
materials that can be considered oligomers or polymers of
halogenated monomers. Examples of these monomers include
tetrabromobisphenol A (TBBPA) and dibromostyrene (DBS), which have
the following structures:
##STR00003##
[0007] Commercially, TBBPA and DBS are typically not used in their
monomeric form, but are converted into an oligomeric or polymeric
species. One class of oligomers is the brominated carbonate
oligomers based on TBBPA. These are commercially available from
Chemtura Corporation (examples include Great Lakes BC-52, Great
Lakes BC-52HP.TM., and Great Lakes BC-58.TM.) and by Teijin
Chemical (FireGuard 7500 and FireGuard 8500). These products are
used primarily as flame retardants for polycarbonate and
polyesters.
[0008] Brominated epoxy oligomers, based on condensation of TBBPA
and epichlorohydrin, are commercially available and sold by
Dainippon Ink and Chemicals under the Epiclon.RTM. series, and also
by ICL Industrial Products (examples are F-2016 and F-2100) and
other suppliers. The brominated epoxy oligomers find use as flame
retardants for various thermoplastics both alone and in blends with
other flame retardants.
[0009] Another class of brominated polymeric flame retardants based
on TBBPA is exemplified by Teijin FG-3000, a copolymer of TBBPA and
1,2-dibromoethane. This aralkyl ether finds use in ABS and other
styrenic polymers. Alternative end-groups, such as aryl or methoxy,
on this polymer are also known as exemplified by materials
described in U.S. Pat. No. 4,258,175 and U.S. Pat. No. 5,530,044.
The non-reactive end-groups are claimed to improve the thermal
stability of the flame retardant.
[0010] TBBPA is also converted into many other different types of
epoxy resin copolymer oligomers by chain-extension reactions with
other difunctional epoxy resin compounds, for example, by reaction
with the diglycidylether of bisphenol A. Typical examples of these
types of epoxy resin products are D.E.R..TM. 539 by the Dow
Chemical Company, or Epon.TM. 828 by Hexion Corporation. These
products are used mainly in the manufacture of printed circuit
boards.
[0011] DBS is made for captive use by Chemtura Corporation and is
sold as several different polymeric species (Great Lakes
PDBS.sub.--80.TM., Great Lakes PBS-64HW.TM., and Firemaster
CP44-HF.TM.) to make poly(bromostyrene) type flame retardants.
These materials represent homopolymers or copolymers. Additionally,
similar brominated polystyrene type flame retardants are
commercially available from Albemarle Chemical Corporation
(Saytex.RTM. HP-3010, Saytex.RTM. HP-7010, and PyroChek 68PB). All
these polymeric products are used to flame retard thermoplastics
such as polyamides and polyesters.
[0012] Unfortunately, one of the key drawbacks of the existing
brominated polymer materials is their relatively low bromine
content, which makes them less efficient as a flame retardant and
consequently typically has a negative effect on the desirable
physical properties of the flame retardant formulations containing
them, such as impact strength. For example, whereas deca and
deca-DPE contain 82-83% bromine, oligomers or polymers based on the
brominated monomers mentioned above generally have a bromine
content in the range of 52%-68%, depending on the material. This
therefore typically requires a flame retardant loading level in a
polymer formulation significantly higher than that required for
deca, often resulting in inferior mechanical properties for the
formulation.
[0013] Other considerations also influence the impact the flame
retardant has on the final properties of the formulated resin.
These considerations include the flame retardant thermal stability
and the compatibility with the host resin. In situations where
these other considerations are relatively constant, the bromine
content, and hence flame retardant load level, has a major
influence on the properties of the overall formulation.
[0014] To address the need for flame retardant materials that to
not detract from the mechanical properties of the target resin, we
have now developed a family of materials that can be classified as
halogenated, and particularly brominated, aryl ether oligomers. In
particular, we have found that the use of these halogenated aryl
ether oligomers results in superior mechanical properties in resins
such as HIPS and polyolefins and that the materials also provide
excellent properties in engineering thermoplastics such as
polyamides and polyesters. The aryl ether oligomers can be
halogenated to a higher level than the oligomers and polymers that
are commercially available today, which should have a positive
effect on their mechanical property performance. It is also found
that these aryl aryl ether oligomers, even at lower levels of
halogenation, give formulations with acceptable mechanical
properties Japanese Unexamined Patent Application Publication
2-129,137 discloses flame retardant polymer compositions in which
the polymer is compounded a with halogenated
bis(4-phenoxyphenyl)ether shown by general formula [I]:
##STR00004##
in which X is a halogen atom, a and d are numbers in the range of
1-5, and b and c are numbers in the range of 1-4. However, the
flame retardant is produced by brominating the
bis(4-phenoxyphenyl)ether as a discrete compound and not an
oligomeric material obtained by polymerizing an aryl ether monomer.
In contrast, employing a material having an oligomeric distribution
as in the present invention is believed to improve its performance
properties as a flame retardant.
[0015] In an article entitled "Synthesis and Stationary Phase
Properties of Bromo Phenyl Ethers, Journal of Chromatography, 267
(1983), pages 293-301, Dhanesar et al disclose a process for the
site-specific bromination of phenyl ethers containing from 2 to 7
benzene rings. Again the ethers appear to be discrete compounds
with no oligomeric distribution and, although the products are said
to be useful in the separation of organic compounds, no reference
is given to their possible use as flame-retardants.
SUMMARY
[0016] In one aspect, the present invention resides in a
halogenated aryl ether oligomer formed by halogenation of an aryl
ether oligomer.
[0017] Conveniently, the halogen content of the halogenated aryl
ether oligomer is in the range of about 50 to about 83 wt %, such
as in the range of about 65 to about 80 wt % of the oligomer.
Generally, the halogen comprises bromine.
[0018] Conveniently, the halogenated aryl ether oligomer has an
average of least 3 aryl and typically at least 5 aryl rings.
Generally, the molecular weight of the halogenated oligomer is up
to 1,000,000 Daltons.
[0019] In one embodiment, the halogenated aryl ether oligomer
comprises the following repeating monomeric units:
##STR00005##
wherein R is hydrogen or alkyl, especially C.sub.1 to C.sub.4
alkyl, Hal is halogen, normally bromine, m is at least 1, n is 0 to
3 and x is at least 2, such as 3 to 100,000, for example 5 to
20.
[0020] In a further aspect, the present invention resides in a
flame retardant polymer composition comprising (a) a flammable
macromolecular material and (b) a halogenated aryl ether oligomer
flame retardant formed by halogenation of an aryl ether
oligomer.
[0021] In yet a further aspect, the present invention resides in a
flame retardant polymer composition comprising (a) a flammable
macromolecular material and (b) a halogenated aryl ether oligomer
flame retardant formed by halogenation of an aryl ether oligomer
wherein said halogenated aryl ether oligomer comprises the
following repeating monomeric units:
##STR00006##
wherein R is hydrogen or alkyl, especially C.sub.1 to C.sub.4
alkyl, Hal is halogen, normally bromine, m is at least 1, n is 0 to
3 and x is at least 2, such as 3 to 100,000, for example 5 to
20.
[0022] Conveniently, said halogenated aryl ether oligomer also
comprises end groups each independently comprising an alkyl,
alkoxy, aryl, aryloxy, hydrogen, halogen or hydroxyl group.
[0023] In still yet a further aspect, the present invention resides
in a flame retardant polymer composition comprising (a) a flammable
macromolecular material and (b) a halogenated aryl ether flame
retardant having the following formula:
##STR00007##
wherein each R.sup.1 is independently selected from hydrogen,
hydroxy, halogen and alkyl, wherein each R.sup.2 is independently
selected from hydrogen, hydroxy, halogen and alkyl, provided at
least one R.sup.2 and normally at least one R.sup.1 is halogen,
normally bromine, n is 5, m is 4, and x is from 1 to 10, for
example from 2 to 6.
[0024] Conveniently, the flammable macromolecular material (a) is a
thermoplastic polymer, such as polystyrene, poly(acrylonitrile
butadiene styrene), a polycarbonate, a polyolefin, a polyester
and/or a polyamide.
[0025] In one embodiment, the flammable macromolecular material (a)
is polystyrene and the amount of halogenated aryl ether oligomer
flame retardant in the composition is between about 5 and 25 wt %,
such as between about 10 and 20 wt %.
[0026] In another embodiment, the flammable macromolecular material
(a) is polypropylene and the amount of halogenated aryl ether
oligomer flame retardant in the composition is between about 20 and
50 wt %, such as between about 25 and 40 wt %.
[0027] In a further embodiment, the flammable macromolecular
material (a) is polyethylene and the amount of halogenated aryl
ether oligomer flame retardant in the composition is between about
5 and 35 wt %, such as between about 20 and 30 wt %.
[0028] In a further embodiment, the flammable macromolecular
material (a) is a polyamide or a polyester and the amount of
halogenated aryl ether oligomer flame retardant in the composition
is between about 5 and 25 wt %, such as between about 10 and 20 wt
%.
[0029] Alternatively, the flammable macromolecular material (a) is
a thermosetting polymer, such as an epoxy resin, an unsaturated
polyester, a polyurethane and/or a rubber.
DESCRIPTION OF THE EMBODIMENTS
[0030] Described herein is a halogenated aryl ether oligomer formed
by halogenation, particularly bromination, of an aryl ether
oligomer and use of the halogenated oligomer as a flame retardant
for flammable macromolecular polymers. Suitable macromolecular
polymers include thermoplastic polymers, such as polystyrene,
poly(acrylonitrile butadiene styrene), polycarbonates, polyolefins,
polyesters and polyamides, and thermosetting polymers, such as
epoxy resins, unsaturated polyesters, polyurethanes and
rubbers.
[0031] The term "oligomer" is used herein to mean a compound formed
by oligomerization of one or more monomers so as to have repeating
units derived from said monomer(s) irrespective of the number of
said repeating units. Because the aryl ether precursor used to the
produce the present flame retardant is produced by an
oligomerization process, the precursor and the halogenated product
will generally have a distribution of molecular weight. In
particular, the oligomer generally has an average of least 3 aryl
and typically at least 5 aryl rings, with the average molecular
weight of the halogenated oligomer being up to 1,000,000
Daltons.
[0032] Typically, the present halogenated aryl ether oligomer
comprises the following repeating monomeric units:
##STR00008##
wherein R is hydrogen or alkyl, especially C.sub.1 to C.sub.4
alkyl, Hal is halogen, m is at least 1, n is 0 to 3 and x is at
least 2, such as 3 to 100,000, for example 5 to 20. The halogen can
be fluorine, chlorine, bromine and/or iodine, especially bromine.
Generally, the halogenated aryl ether oligomer also comprises end
groups each independently comprising an alkyl, alkoxy, aryl,
aryloxy, hydrogen, halide or hydroxyl group.
[0033] In one embodiment, the halogenated aryl ether oligomer flame
retardant has the following formula:
##STR00009##
wherein each R.sup.1 is independently selected from hydrogen,
hydroxy, halogen and alkyl, wherein each R.sup.2 is independently
selected from hydrogen, hydroxy, halogen and alkyl, provided at
least one R.sup.2 is halogen, normally bromine, n is 5, m is 4, and
x is from 1 to 100,000, for example from 3 to 20.
[0034] Generally, the halogen content of the present halogenated
aryl ether oligomer is in the range of about 50 to about 83 wt %,
such as in the range of about 65 to about 80 wt % of the
oligomer.
[0035] In another embodiment, the flame retardant used herein
comprises a halogenated aryl ether having the following
formula:
##STR00010##
wherein each R.sup.1 is independently selected from hydrogen,
hydroxy, halogen and alkyl, wherein each R.sup.2 is independently
selected from hydrogen, hydroxy, halogen and alkyl, provided at
least one R.sup.2 and normally at least one R.sup.1 is halogen,
normally bromine, n is 5, m is 4, and x is from 1 to 10, for
example from 2 to 6. In the case of this embodiment, the
halogenated aryl ether may have an oligomeric distribution or may
be a discrete compound.
[0036] The present flame retardant is produced by halogenation,
normally bromination, of a polyaryl ether precursor, which in turn
can be made by oligomerization of a hydroxyhaloaryl material, such
as bromophenol, or reaction of a dihalo aryl material, such as
dibromobenzene, with a dihydroxyaryl material, such as resorcinol,
using an ether synthesis, such as the Ullmann ether synthesis. In
this process, the reagents are heated under reflux, typically at
about 125.degree. C. to about 200.degree. C., in a polar organic
solvent, such as N,N-dimethylformamide or benzophenone, in the
presence of a strong base and a copper-containing catalyst.
[0037] A representative disclosure of the Ullmann ether synthesis
is given by Laskoski et al. in "Oligomeric Cyanate Ester Resins:
Application of a Modified Ullmann Synthesis in the Preparation of
Thermosetting Polymers", Journal of Polymer Science. Part A.
polymer Chemistry, Vol. 44, (2006), pages 4559-4565.
[0038] Bromination of the resultant polyaryl ether is readily
achieved by the reaction of the polyaryl ether with bromine in the
presence of a Lewis acid catalyst, such as aluminum chloride.
Depending on the amount of bromine desired to be introduced into
the aryl ether oligomer, the weight ratio of bromine to oligomer
employed in the bromination reaction is typically between about 1:1
and about 100:1, such as between about 3:1 and about 20:1. The
final brominated aryl ether oligomer is generally arranged to have
at least one, and typically between 2 and 4 bromine atoms per aryl
ether repeating unit of the oligomer.
[0039] Alternatively, bromine chloride may be used as the
brominating agent to generate the desired product in similar
fashion. In this case, a small amount of organically-bound chlorine
would also be present, but would not detract from the properties of
the final flame retardant.
[0040] The resultant halogenated aryl ether oligomer can be used as
a flame retardant for many different polymer resin systems because
of its high thermal stability and also because of its relatively
high halogen content compared with existing polymeric flame
retardant products, such as brominated polystyrenes. Generally, the
halogenated aryl ether oligomer is employed as a flame retardant
with thermoplastic polymers, such as polystyrene, high-impact
polystyrene (HIPS), poly(acrylonitrile butadiene styrene) (ABS),
polycarbonates (PC), PC-ABS blends, polyolefins, polyesters and/or
polyamides. With such polymers, the level of the halogenated
oligomer in the polymer formulation required to give a V-0
classification when subjected to the flammability test protocol
from Underwriters Laboratories is generally within the following
ranges:
TABLE-US-00001 Polymer Useful Preferred Polystyrene 5 to 25 wt % 10
to 20 wt % Polypropylene 20 to 50 wt % 25 to 40 wt % Polyethylene 5
to 35 wt % 20 to 30 wt % Polyamide 5 to 25 wt % 10 to 20 wt %
Polyester 5 to 25 wt % 10 to 20 wt %.
[0041] The present halogenated aryl ether oligomer can also be used
with thermosetting polymers, such as an epoxy resins, unsaturated
polyesters, polyurethanes and/or rubbers. Where the base polymer is
a thermosetting polymer, a suitable flammability-reducing amount of
the oligomer is between about 5 wt % and about 35 wt %, such as
between about 10 wt % and about 25 wt %.
[0042] Typical applications for polymer formulations containing the
present halogenated aryl ether oligomer as a flame retardant
include automotive molded components, adhesives and sealants,
fabric back coatings, electrical wire and cable jacketing, and
electrical and electronic housings, components and connectors. In
the area of building and construction, typical uses for the present
flame retardant include self extinguishing polyfilms, wire
jacketing for wire and cable, backcoating in carpeting and fabric
including wall treatments, wood and other natural fiber-filled
structural components, roofing materials including roofing
membranes, roofing composite materials, and adhesives used to in
construction of composite materials. In general consumer products
the present flame retardant can be used in formulation of appliance
parts, housings and components for both attended and unattended
appliances where flammability requirements demand.
[0043] The invention will now be more particularly described with
reference to the following non-limiting Examples.
Examples 1 to 7
Bromination of Aryl Ether Resin
[0044] Bromine (3176 g, 19.87 mol) was added to a solution of 500 g
of aryl ether resin (Santovac OS-124) in 1 L of dichloroethane
containing 6.5 g of AlCl.sub.3 catalyst. The Santovac OS-124 is an
aryl ether resin containing five aryl rings connected in the meta
position and was used to simulate an oligomeric material. After
work-up, the brominated resin was isolated to give 2013.6 g of a
pale cream powder as the product. The material analyzed to contain
75.7% bromine and the TGA analysis showed a 5% wt loss at
420.degree. C. Differential Scanning Calorimetry (DSC) analysis
showed a glass transition (Tg) at 154.degree. C.
[0045] Several additional materials were prepared in similar
fashion to give brominated aryl ether materials containing
different levels of bromine or different ring connectivities, as
shown in Table 1. The bromination level was found to influence the
observed glass transition temperatures and melt-ranges of the
products.
TABLE-US-00002 TABLE 1 Oligomer % Tg, .degree. C. Visual Melt
Example Type.sup.(a) Bromine (DSC) Range, .degree. C. 1 5-meta 75.7
154 177-211 2 5-meta 65.5 77.0 87-109 3 5-meta 74.7 150.8 160-183 4
5-meta 80.0 192.1 204-221 5 6-meta 74.8 160.5 184-198 6 3-para 72.6
85.3 185-241 7 4-para 70.8 130.5 168-196 .sup.(a)Nomenclature:
5-meta means 5 aryl rings connected by all meta linkages.
Example 8
Polyarylether Synthesis from Resorcinol and 1,4-Dibromobenzene
[0046] A reaction flask was charged with resorcinol (15.0 g, 0.137
mole), 1,4-dibromobenzene (32.3 g, 0.137 mole),
N,N-dimethylformamide (205 g; 2.58 mole), toluene (20 g, 0.22
mole), and a 50% solution of KOH, which was made by dissolving 90%
KOH (17.05 g, 0.274 mole) in DI water. The amount of base typically
ranges from 1.8 to 2.2 mole per mole of resorcinol. The reaction
mixture was heated to reflux to azeotropically remove the water.
After the theoretical amount of water was removed, most of the
toluene was stripped from the reaction flask to a final pot
temperature of 148-150.degree. C. Then, the reaction was cooled to
-120.degree. C. and CuI (0.52 g, 0.00274 mole) and
1,10-phenanthroline (0.74 g, 0.0041 mole) were added simultaneously
under a heavy nitrogen stream. The reaction flask was blanketed
under nitrogen and the mass heated to reflux
(.about.150-155.degree. C.) for 24 hour and then cooled for workup.
The worked up involved acidification of the mixture to a pH of 2-3
with 2% HCl followed by extraction with methylene chloride or
chloroform. The organic phase was stripped to give a viscous resin
product residue with an isolated yield=92%. GPC analysis of the
product gave a molecular weight (Mw) of 605 and polydispersity (Pd)
of 1.97.
[0047] GPC analysis of various reaction products produced by this
approach gave an Mw ranging from 600 to 3100.
Example 9
Polyarylether Synthesis from 3-Bromophenol in DMF/Toluene
[0048] 3-Bromophenol (100 g, 0.58 mole), toluene (700 g), and 50%
KOH (72 g, 0.58 mole) were added to a standard reaction flask. The
contents were heated to reflux and the water was removed
azeotropically. An additional 540 grams of toluene was stripped
from the reaction flask. The contents of the flask were cooled to
100.degree. C. and DMF (467 grams), CuI (0.22 g, 0.0012 mole), and
1,10-phenanthroline (0.31 g, 0.0017 mole) were added. The contents
of the flask were heated back to reflux. Additional toluene was
stripped until the temperature reached 140.degree. C. and
bromobenzene (4.55 grams, 0.029 mole) was then added. After the
reaction was complete, the product was worked up to give a viscous
amber colored resin in 93.1% yield. This product polymer had a
molecular weight by GPC analysis of 2270 Mw.
Example 10
Polyarylether Synthesis from 4-Bromophenol with Benzophenone as
Solvent
[0049] A reaction flask was charged with 4-bromophenol (232.5 g,
1.34 mole), benzophenone (1435 g, 8.04 mole), and toluene (900 g,
1.34 mole). The flask was purged with N.sub.2 and was heated to
<100.degree. C. to dissolve the benzophenone. A 50% solution of
KOH was prepared by dissolving 90% KOH (83.5 g, 1.34 mole) in 83.5
g DI water. The KOH solution was added to the flask over a period
of 5 minutes and contents of the flask were heated to reflux. The
water was removed azeotropically and the toluene was distilled out.
Bromobenzene (10.5 g, 0.07 mole) was added along with a solution of
CuCl (1.33 g, 0.0134 mole) dissolved in pyridine (90 g, 0.134
mole). The reaction was held at 204.degree. C. for 5 hours. The
reaction was cooled and worked up to give 165.7 g (65% yield) of
light tan solids. Analysis by GPC (THF solvent system) gave Mw=1790
and Pd=1.70 (not all the material was soluble).
[0050] Due to lack of complete solubility in the solvent used for
GPC determinations, a secondary analysis of molecular weight was
conducted based on DSC. A series of model compounds of para aryl
ethers containing 3, 4, and 5 rings were analyzed by DSC and found
to have melting points that fit to a straight line equation.
Included in this analysis was diphenyl ether, which fit the line as
expected. The mp data is as follows for the para model series (2
ring through 5 ring): 26, 75.6, 108.2, 147.4.degree. C. This line
was used to estimate the number of aryl groups on the polymer that
was made, which would only be a crude estimation of molecular
weight. By this approach, the number of aryl rings was predicted to
be 8.
Examples 11 and 12
Bromination of Aryl Ethers from 4-Bromophenol Polymerization
[0051] A reaction flask was charged with 100.0 g of the polyphenyl
ether produced in Example 10, 600 ml of chloroform and 10.2 g of
aluminum chloride. The resulting slurry was heated to reflux
(60.degree. C.) and 1202.8 g of dry bromine was added over 6 hours
while maintaining reflux. The reaction mass was held at reflux
temperature for 2 hours and worked up to give a solid precipitate.
The resulting polymeric product (223.2 g), was a tan solid, with
the following analysis: 68.8% OBr, melt range 230-313.degree. C.
The properties of the product are shown in Table 2.
[0052] The above bromination method was repeated to give a
brominated oligomeric aryl ether material containing a different
level of bromine, as shown in Table 2.
Examples 13 and 14
Bromination of Aryl Ethers from 3-BrPhOH Polymerization
[0053] A large-scale reaction from Example 9 was conducted by using
a 0.20 mol ratio of bromobenzene endcap to 3-bromophenol,
generating a material that analyzed to have a slightly lower
molecular weight by GPC of 700 Mw. A reaction flask was charged
with 108.2 g of this polyphenyl ether, 1000 ml of chloroform and
10.8 g of aluminum chloride. The resulting slurry was heated to
reflux (60.degree. C.) and 1044.1 g of dry bromine was added over 8
hours while maintaining reflux. The reaction mass was held at
reflux temperature for 1 hour and worked up to give a solid
precipitate. The resulting polymeric product (319.9 g), was a brown
solid, with the following analysis: 70.2% OBr, melt range
141-161.degree. C., DSC showed a glass transition (Tg) at
117.degree. C. The properties of the product are shown in Table
2.
[0054] The above bromination method was repeated to give a
brominated oligomeric aryl ether material containing a different
level of bromine, as shown in Table 2.
[0055] By comparing the results in Table 2, it will be seen that by
varying the regiochemistry of the oligomer (meta vs para),
oligomers with different glass transition temperatures and visual
melt-ranges were produced. It is also possible to prepare a mixed
oligomer having a blend of meta and para connectivities by using
the appropriate reagents and ratios during the reaction.
TABLE-US-00003 TABLE 2 Oligomer GPC % Tg, .degree. C. Melt Example
Type (MW).sup.(a) Bromine (DSC) Range, .degree. C. 11 Para 1790
68.8 >240 230-313 12 Para 1700 58.7 >240 216-293 13 Meta 700
70.2 117 141-161 14 Meta 1020 64.1 123 141-164 .sup.(a)GPC analysis
was conducted on the oligomer prior to bromination. The para
samples were only partially soluble.
Example 15
Compounding of Brominated Aryl Ether Oligomers in HIPS Resin
[0056] The brominated aryl ether oligomers prepared in Examples 1
to 4 (Table 1) were separately compounded with HIPS (high impact
polystyrene) resin formulations containing antimony oxide (ATO)
synergist using a twin-screw extruder with barrel temperatures of
200-220.degree. C. For comparison, similar formulations were
prepared using deca and deca-DPE as the flame retardants. The
resultant formulations were injection-molded into test bars and
evaluated as shown in Table 3. The mechanical property and MFI
tests were conducted according to the normal ASTM methods. The
glass-transition temperatures of the brominated aryl ether
oligomers were all below the compounding temperatures of the resin,
indicating that the oligomers would be melt-blendable in this
system. Note that deca and deca-DPE are not melt-blendable and act
as filler type materials. This data shows correlation between melt
flow index (MFI) of the compounded material and the Tg of the FR
that was used, which is somewhat expected. The data also shows that
the Vicat softening point is not really influenced by the flame
retardant type that was used, except for the lower Tg sample, which
is also reasonable.
TABLE-US-00004 TABLE 3 Formulation No 15-A 15-B 15-C 15-D 15-E 15-F
FR Deca Deca-DPE Example 1 Example 2 Example 3 Example 4 FR, % Br
83 "83" 75.7 65.5 74.7 80.0 FR Tg, .degree. C. NA NA 154 77 151 192
Formulation Polystyrene Resin 77.3 77.3 75.95 73.6 75.7 76.8 FR
14.0 14.0 15.35 17.7 15.6 14.5 ATO 3.5 3.5 3.5 3.5 3.5 3.5 Anox
PP-18 0.2 0.2 0.2 0.2 0.2 0.2 Kraton D1101 5.0 5.0 5.0 5.0 5.0 5.0
Test Results MFI (g/10 min) 9.7 7.7 9.4 19.2 9.7 8.9 Vicat,
.degree. C. 96.2 97.6 98.7 92.9 99.2 100.4 Izod Notched Impact
Strength 2.1 2.05 3.2 2.5 2.7 2.5 (ft-lb/in) UL-94 ( 1/16'') V-0
V-0 V-0 V-0 V-0 V-0
[0057] The surprising result lies in the impact strength data. When
comparing the formulations with the two control samples, the aryl
ether oligomer systems show an actual increase in impact strength.
A wide range of Tg can be used while still obtaining good
mechanical properties. This result could be due to an improvement
in resin-FR compatibility, domain size of the FR material in the
test bars, or some other factor. These data indicate that the
properties of the final formulation can be optimized by adjusting
the FR oligomer glass transition temperature. This would not be
possible with brominated small molecules, as they typically are
high-melting solids.
Example 16
Compounding of Brominated Aryl Ether Oligomers in HIPS Resin
[0058] The brominated aryl ether oligomers prepared in Example 12
(Table 2) were separately compounded with HIPS (high impact
polystyrene) resin formulations containing antimony oxide synergist
using a twin-screw extruder with barrel temperatures of
200-220.degree. C. These formulations were injection-molded into
test bars and evaluated as shown in Table 4. Two of these FR
oligomer materials have Tg values below the compounding
temperatures and two have Tg values somewhere above that
temperature. The latter two would, therefore, not be melt-blendable
and the resulting MFI values are expectedly lower. Interestingly,
these samples based on the para aryl ether gave reduced impact
strength properties and those based on the meta aryl ethers gave
good impact strength values. This could be a reflection of
different compatibilities between the FR types and the resin, or
related to how the materials coalescence in formulation upon
cooling, or some other factor.
TABLE-US-00005 TABLE 4 Formulation No. 16-A 16-B 16-C 16-D 16-E FR
Deca Example Example Example Example 12 11 13 14 FR, % Br 83 58.7
68.8 70.2 64.1 FR Tg, .degree. C. NA >240 >240 117 123
Formulation Polystyrene Resin 77.3 71.5 74.4 74.55 73.2 FR 14.0
19.8 16.9 16.55 18.1 ATO 3.5 3.5 3.5 3.5 3.5 Anox PP-18 0.2 0.2 0.2
0.2 0.2 Kraton D1101 5.0 5.0 5.0 5.0 5.0 Test Results MFI (g/10
min) 9.7 5.6 5.7 12.1 11.7 Vicat, .degree. C. 96.2 99.6 98.2 97.8
98.1 Izod Notched 2.1 1.2 0.7 2.2 1.9 Impact Strength (ft-lb/in)
UL-94 ( 1/16'') V-0 V-1 V-1 V-0 V-0
Example 17
Compounding of Brominated Aryl Ether Oligomers in HIPS Resin
[0059] Since the impact strength for some of the formulations in
Examples 15 and 16 was actually higher than the standard deca type
control runs, a study was conducted in which the flame retardant of
Example 1 was employed and impact modifier (Kraton D1101) was
reduced, as shown in Table 5. This study shows that the impact
modifier can indeed be reduced or potentially eliminated from a
HIPS formulation and still be as good as (or close to) the deca
control formulation, and that there is room for further formulation
optimization of properties.
TABLE-US-00006 TABLE 5 Formulation No 17-A 17-B 17-C 17-D FR Deca
Example 1 Example 1 Example 1 FR, % Br 83 73.1 73.1 73.1 FR Tg,
.degree. C. NA 148 148 148 Formulation Polystyrene Resin 77.3 75.9
78.4 80.9 FR 14.0 15.4 15.4 15.4 ATO 3.5 3.5 3.5 3.5 Anox PP-18 0.2
0.2 0.2 0.2 Kraton D1101 5.0 5.0 2.5 0 Test Results MFI (g/10 min)
9.7 12.5 14.3 15.5 Vicat, .degree. C. 96.2 99.3 99.1 98.6 Izod
Notched Impact 2.1 2.6 2.2 1.8 Strength (ft-lb/in) UL-94 ( 1/16'')
V-0 V-0 V-0 V-0
Example 18
Compounding of Brominated Aryl Ether Oligomers in Polyamide
[0060] The brominated aryl ether oligomers shown in Table 1 were
compounded with glass-reinforced PA66 resin containing antimony
oxide synergists. These formulations were molded into test bars and
evaluated as shown in Table 6. This set of data compares the
oligomeric aryl ether flame retardants with a commercially
available brominated polystyrene (Saytex.TM. HP-3010). The results
show that the aryl ether is more efficient, showing a V-0 at 13.3%
loading and a strong V-0 at 16% loading, as compared with the 20%
loading for the HP-3010 material. The data also shows a slight
improvement in mechanical properties with tensile strength being
about the same, but tensile elongation showing about a 20%
improvement.
TABLE-US-00007 TABLE 6 Formulation No. 18-A- 18-B 18-C 18-D 18-E FR
None HP-3010 Ex. 1 Ex. 1 Ex. 2.sup.a FR, % Br -- 68 75.7 75.7 63.0
Formulation PA66 Resin 70 41.2 50.65 47.15 42.65 Glass Fiber 30 30
30 30 30 FR 20 13.5 16.0 19.8 ATO 8.45 5.5 6.5 7.2 Magnesium
stearate 0.35 0.35 0.35 0.35 Test Results Tensile Strength, Kpsi
26.9 21.3 21.4 21.0 NA Tensile Elongation, % 3.91 1.89 2.39 2.22 NA
Sprial flow, in. 23.8 30.4 26.3 28.2 NA Viscosity, Pa-s @ 168.8
103.2 106.0 100.8 NA 1000 s.sup.-1 UL-94 total burn time NA 5 36 2
14 (5 bars), s UL-94 ( 1/32'') FAIL V-0 V-0 V-0 V-0 .sup.aA
scale-up of Example 2; Analysis: m.p. 96-113.degree. C., % Bromine
= 63.0%
[0061] In order to determine if the improved flame retardant
efficiency is a result of the higher bromine content, or is related
to the structure of the oligomer, a lower bromine content sample
was also tested. The results showed that at the same load level as
the 68% bromine content brominated polystyrene material (i.e. lower
overall bromine content), the formulation was a strong V-0. This
indicated that the structure is contributing to the improved FR
efficiency.
Example 19
Compounding of Different Flame Retardants in Polypropylene
[0062] The brominated aryl ether oligomer of Example 3 was
compounded with Profax 6323 polypropylene homopolymer containing an
antimony oxide synergist and, for comparison, similar formulations
were prepared using deca and deca-DPE as the flame retardant. The
formulations were compounded using a twin-screw extruder with
barrel temperature of about 200.degree. C., injection-molded into
test bars and evaluated as shown in Table 7.
TABLE-US-00008 TABLE 7 Formulation No 19-A 19-B 19-C 19-D Profax
6323 PP homopolymer (%) 100 59 55.8 59 Deca (%) 35 Bromo(polyaryl
ether) Ex. 3 (%) 38.2 Deca-BDE (%) 35 ATO (%) 6 6 6 UL-94 Rating
V-0 V-0 V-0 MFI (g/10 min) 12.4 11.2 47.4 12.1 HDT (.degree. C.),
264 psi 84 112 120 117
[0063] These results show a significant increase in the melt flow
property with a slightly higher increase in Heat Deflection
Temperature (HDT) for the oligomeric FR product as compared with
the deca and deca-DPE control samples.
[0064] The formulations were also subjected to a bloom test by
placing the UL test bars in an oven at 80.degree. C. The bars were
pulled out of the oven at 24 hours and after 1 week and wiped with
a black cloth to pick up bloom if present. Bloom is a migration of
the flame retardant or other additive to the surface and usually
shows as a visible dust on the test cloth. There was no bloom
present on the oligomeric FR formulation bars, whereas the other
two flame retardant formulations showed bloom.
Example 20
Compounding of Different Flame Retardants in Low Density
Polyethylene
[0065] The brominated aryl ether oligomer of Example 3 was
compounded with Petrothene NA820000 NT low density polyethylene
and, for comparison, similar formulations were prepared using deca
and deca-DPE as the flame retardant. The formulations were
compounded using a twin-screw extruder with barrel temperature of
about 190.degree. C., injection-molded into test bars and evaluated
as shown in Table 8.
TABLE-US-00009 TABLE 8 Formulation No 20-A 20-B 20-C 20-D Resin
Petrothene NA820000 NT LDPE FR None Deca Ex. 3 Deca-BDE FR % 24
26.2 24 MFI (g/10 min) 1.33 1.54 2.38 1.35 HDT (.degree. C.), 264
psi 39.6 42.1 66.9 42.3 Flexural Properties Strength (ksi) 1.2 1.5
2.3 1.5 Modulus (ksi) 19.1 27.1 56.5 27 UL-94 Rating FAIL V-0 V-0
V-0
[0066] For this resin system, the MFI and HDT properties both
increased when the oligomeric flame retardant was used as compared
the brominated control samples. Additionally, it was found that the
flexural properties also increased. A bloom test was conducted as
described in the previous example and the oligomeric FR formulation
showed just a faint trace of bloom, whereas the deca formulation
showed a large amount of bloom on the test cloth.
[0067] While the present invention has been described and
illustrated by reference to particular embodiments, those of
ordinary skill in the art will appreciate that the invention lends
itself to variations not necessarily illustrated herein. For this
reason, then, reference should be made solely to the appended
claims for purposes of determining the true scope of the present
invention.
* * * * *