CA1274648A - Flame retardant wire coating compositions - Google Patents

Abstract

FLAME RETARDANT WIRE COATING COMPOSITIONS

ABSTRACT OF THE DISCLOSURE

Flame retardant silicone-polyimides are provided having improved elongation which are useful as wire coating compositions.

Description

~Z~4~ RD-163~4 .
, FLAME RETARDANT WIRE COATING CO~OSITIONS

BACKGROUND OF_THE INVENTION

Prior to the present invention, as shown by Holub, U.S. Patent 3,325,450, polysiloxane imides useful as insula-tion for electrical conductors were prepared by effecting reaction between a diaminopolysiloxane and benzophenonedi-anhydride in the presence of a suita~le organic solvent, such as dimethylformamide, N-methyl-2-pyrrolidone, cresol, etc. The initial reaction was generally carried out from room temperature to 150C resulting in the production of an intermediate polyamide acid derivative. Thereafter, the solvent was removed from the resulting amide acid derivative by heating at temperatures of from about 150~C to 400DC to effect cyclization and formation of the imide structure.
A similar procedure is shown by Greber, Polykon-densationsreaktionen Bifunktioneller Siliciumorganischer Verbindungen, Journal fur praktische Chemie. Band 313, HEFT
3, 1971, S. 461-483, J.A. Barth, Leipzig. Although the procedure of Greber is somewhat different from that shown by Holub, both Holub and Greber utilize a dipolar aprotic solvent, such as dimethylacetamide to form a solution of a silicone-polyamide acid from which films can be cast onto a --1-- ~ ..

~Z7~8 substrate and further heating is required to effect the cyclization of the polyamide acid to the polyimide state.
Improved results in methods for making silicone-pol~imides can be obtained by utilizing aromatic bis(ether a~hydride) or the corresponding tetracarboxylic acid in combination with amino alkylene terminated polydiorgano-siloxanes as shown, for example, by Takekoshi et al., U.S.
Patent 3,833,546 and Heath et al., U.S. Patent 3,847,867, assigned to the same assignee as the present invention.
Although silicone-polyimides have long been recognized for their potential as a source for extrudable wire coating insulation, the flammability requirements o~
the wire çoating industry has generally restricted the use of these materials. In addition to flame retardance, wire coating fabricators also favor extrudable wire coating insulation having at least 150% elongation at break when pulled-laterally from a clamped portion of the extrudate along the wire surface. However, efforts to increase the elongation characteristics of silicone-polyimide by increas-ing the weight percent of silicone has generally been foundto increase the flammability of the silicone-polyimide.
The present invention is based on a discovery that silicone-polyimide utili7ing aromatic bis(ether anhydride) and amino alkylene termi~ated polydiorganosiloxane having a critical block length can be extruded onto wire and exhibit an elongation percent of 150 or greater-while satisfying UL
94 flammability requirements as defined hereinafter. Wire coating industry requirements can be satisfied providing a critical relationship is maintained between the polydior-ganosiloxane block length and the weight percen' siliconewhich is preferably 25% to 45% by weight based on the weight of silicone-polyimide. Polydiorganosiloxane block lengths having an average value of about 20 diorganosiloxy units or ~7~6~

less has been found to provide effective results, while a block length of about 5 to about 15 chemically combined diorganosiloxy units is preferred.
As used hereinafter, the expressions "flame resistance", "flammable", "nonflammable" or "flame retar-dance" with respect to silicone-polyimide means that the silicon -polyimide has satisfied UL 94 ~-0 requirements for flammability as shown by the Flammability of Plastic Materi-als Bulletin of January 24, 1980. More particularly, a 5" x 1/2" x 1/8" silicone-polyimide test bar was suspended vertically over a 3/4" Bunsen burner flame as provided in the aforementioned UL 94 test. The test sample exhibited a ~4 V-0 rating, which includes the following criteria:
A. Not have any specimens which burn with flaming combustion for more than 10 seconds after either application of the test flame.
B. Not have a total flaming combustion time exceeding 50 seconds for the 10 flame appli-cations for each set of five specimens.
C. Not have any specimens which burn with flaming or glowing combustion up to the holding clamp.
D. Not have any specimens which drip flaming particles that ignite the dry absorbent surgical cotton located 12 inches (305 mm) below the test specimen.
E. Not have any specimens- with glowing combus-tion which persists for more than 30 seconds after the second removal of the test flame.
The silicone polyimides of the present invention can be made by effectin~ reaction between amine terminated polydiorganosiloxane having the formula RD-1635~
~Z7~

( 1 ) NH~-R~iO)~i-R~ 2 and organic dianhydrides, as defined hereinafter, where R is a C(l 14) monovalent hydrocarbon radical or substituted C(l 14) monovalent hydrocarbon radical, Rl is a C(l 14) : divalent hydrocarbon radical or substituted C(l 14) divalent hydrocarbon radical, and n is an integer having an average value of from about 3 to 20 inclusive, and preferably 5 to 15. Rl is preferably C(l 4) polymethylene.

STAT~MENT OF THE INVENTION

There is provided by the present invention, extrudable, flame retardant, silicone-polyimide copolymer comprising by weight, (A) from about 40 to 90% of chemically combined arylimide blocks and (B) from about 10 to 50% of chemically combined polydiorganosiloxane blocks consisting essentially of from about 3 to about 20 diorganosiloxy units, where the organo radicals attached to silicone are selected from monovalent C(l 14) hydrocarbon radicals and substituted monovalent C(1-14) hYdrCarbon radicals.
Chemically combined arylimide blocks which can be present in the silicone-polyimide compositions of the present invention are included within the formula, ~74~4~3 ~/ <~

where R2 is selected from Rl radicals, or the same or different C~l 14) monovalent hydrocarbon radicals and substituted C(l 14) monovalent hydrocarbon radicals, Q i~ a tetravalent radical selected from , and ~ D

D is a member selected from -O-, -S~ NRlN~ oR30~- and -OR Q- -and R3 is a divalent radical selected from P~-16364 ~7~
~H3 ~ . ~r, r~

~3~ ~ 3 C 3 r BrCH3 ~r Br CtCH3) Br r and divalent organic radicals of the general formula, ,:
X is a member selected from the cl~ss consisting of divalent radicals of the formula, c ~ ~ 3 o and -S-p is 0 or 1, y is ~n integer equal to l to 5 inclusive and m is an intPger equal to from 1 to about 60 inclusive.

~7~4~ h~-16364 .~mong the preferred arylimide included within formula (2) there is included aryletherimide of the formula (3) -N ~ o_R4_o ~ _ where R4 is a di~alent aryl radical selected from the class consisting of C~3Br ~rlH3 Br Br ) CH3Br BrCH3 Br r and ~}~xl~

xl is a member selected from the class consisting of RD-1~354 ~LZ7~

yH2y ~ ~, -O- and -S-and p and y are as previously deined.
Radicals included within K of formula (1~ are, for example, C(l 8~ alkyl radicals such as methyl, ethyl, propyl, butyl, pentyl, etc.; C(6 13) aryl radicals such as phenyl, tolyl, xylyl, anthryl; halogenated alkyl and aryl radicals such as chlorophenyl; cyanoalkyl radicals, for example, cyanoethyl, cyanobutyl, trifluoropropyl, etc.
Radicals included within Rl and R2 of formulas (1) and ~2 are, for example, C(l 8) alkylene radicals such as methy-lene, dimethylene, trimethylene, tetramethylene, etc. and arylene radicals such as phenylene, tolylene, xylene, naphthalene, etc.
Organic anhydrides which can be utilized in the practice of the present invention are preferably aromatic bis(etheranhydride)s which are included within the formula,.

(4) ~ I ~ oR40 ~ ~ ~

where R4 is as previously deined. Some of the dianhydriàes included within formula (4~ are, for example,

2,2'-bis~4-(2,3-dicarboxyphenoxy)phenyl]propane dianhydride;
4,4'-bis(2,3-dicarboxyphenoxy~diphenyl ether dianhydride;

- ~D-16364 ~Z7~6~1~

1,3-bis(2,3-dicarboxyphenoxy)benzene dianhydride;
4,4'~bis)2,3 dicarboxyphenoxy)diphenyl sulfide dianhydride;
1,4-bis~2,3-dicarboxyphenoxy)benzene dianhydride;
4,4'-bis(2,3-dicarboxyphenoxy~diphenylsulfone dianhydride, etc.;
2,2-bis[4-(3,4~dicarboxyphenoxy)phenyl]propane dianhydride;
4,4'-bis(3,4-dicarboxyphenoxy)diphenyl ether dianhydride;
4,4'-bis(3,4-dicarboxyphenoxy)diphenyl sulfide dianhydride;
l,3-bis(3,4-dicarboxyphenoxy)benzene dianhydride;
1,4-bis(3,4-dicarboxyphenoxy)benzene dianhydride;
4,4'-bis(3,4-dicarboxyphenoxy)diphenylsulfone dianhydride;
4-(2,3-dicarboxyphenoxy)-4'(3,4-dicarboxyphenoxy)-2,2-diphenylpropane dianhydride, etc.
The dianhydrides of formula (4) can be made in accordance with Webb, U.S. Patent 4,116,980, assigned to the same assignee as the present invention.
In addition to the preferred aromatic bis(ether anhydrides) of formula (4), there can be used other organic dianhydrides in combination with such aromatic bis(ether anhydrides) to make the silicone-polyimide wire coating compositions of the present invention. These organic dianhydrides can be used at up to 50 mole percent based on total dianhydride and include pyromellitic dianhydrides, benzophenone dianhydride and 5,5'-(1,1,3,3-tetramethyl-1,1,3-disiloxanedilyl-bis-norbornane-2,3-dicarboxylic dianhydride.
Procedures for making the aminoorgano terminated polydiorganosiloxane of formula (l) are well known in the l;Z7g~4~

art. For example, aminoorganotetraorganodisiloxane can be eguilibrated with an octaorganocyclotetrasiloxane, such as octamethylcyclotetrasiloxane, to increase the block length of the polydiorganosiloxane. The corresponding aminoorgano-tetraorganodisiloxane, such as aminobutyltetramethyldisilox-ane can be made by the procedure shown by Prober, U.5.
Patent 3,185,719, assigned to the same assignee as the present invention. Prober reacts allylcyanide with di-methylchlorosilane and then hydrolyzes the resulting cyano-propyldimethylchlorosilane in the presence of sodium bicar-bonate to produce the l,3-bis-~ cyanopropyltetramethyl-disiloxane which then can be reduced with hydrogen in the presence of Raney nickel to yield 1,3-bis-~-aminobutyltetra-methyldisiloxane. In a similar manner, 1,3-aminopropyl terminated polydimethyIsiloxane can be obtained by the equilibration of 1,3-bis-~-aminopropyltetramethyldisiloxane which is prepared by utilizing acrylonitrile in a manner similar to that shown for the production of aminobutyltetra-methyldisiloxane utilizing allylcyanide.
In addition to the aminoorganopolydiorganosiloxane in formula (1), there can be utilized in making the sili-cone-polyimides of the present invention, up to about 90 mole percent of aryldiamines based on the total moles of the aminoorganopolydiorganosiloxane of formula (1) and such aryldiamines having the formula - where R5 is a divalent C(6 14) arylene radical.
Included within the arylamines of formula (5) are, for example, m-phenylene diamine;
p-phenylenediamine;

~D-16364 4~

4,4'-diaminodiphenylpropane;
4,4-diaminodiphenylmethane;
benzidine;
4,4'-diaminodiphenyl sulfide;
4,4'-diaminodiphenyl sulfone;
4,4'-diaminodiphenyl ether;
1,5'-diaminonaphthalene;

3,3'-dimethylbenzidine;
3,3'-dimethoxybenzidine;
2,4-bis(~-amino-t-butyl)toluene;
bis(p-~-amino-t-butylphenyl)ether;
bis(p-~-methyl-o-aminopentyl)benzene;
l,3'-diamino-4-isopropylbenzene;
1,2-bis(3-aminopropoxy)ethane;
m-xylylenediamine;
p-xylylenediamine;
2,4-diaminotoluene;
2,6-diaminotoluene.
In instances where aryldiamine of formula (5) is used in combination with the aminoorgano terminated polydi-organosiloxane of formula (l), the weight percent of the aryldiamine is included in the weight percent of the aryl-imide.
The silicone-polyimides can be made by effecting reaction between the organic anhydride, which hereinafter means aromatic bis(ether anhydride) of formula (4) or a mixture thereof with other organic anhydrides, and amino polydiorganosiloxane which hereinafter will mean the amino-organo terminated polydiorganosiloxane of formula (l), or a mixture thereof with aryldiamine of formula (5) in a suit-able organic solvent. Some of the organic solvents which can be used are, for example, dipolar aprotic solvents, such as dimethylformamide, N-methyl-2-pyrrolidone, cresol, ~Z7g~

orthodichlorobenzene, etc. In general, there can be used from about 0.9 to 1.1 mole of the amine functional groups in the terminal position on the aminoorgano terminated polydi-organosiloxane, per mole of the anhydride functional groups of the organic anhydride.
The initial amino-organic anhydride reaction can be carried out from about 100C to 390~C. Reaction can continue until the water of reaction produced during the copolymerization of the organic anhydride and the amino-organo terminated polydiorganosiloxane is achieved and tnewater of reaction is completely removed such as by azeotrop-ing from the reaction mixture. There can be used a typical polymerization catalyst at 0.025 to 1.0% by weight, based on the weight of the reaction mixture, such as an alkali metal aryl phosphinate or alkali metal aryl phosphonate, for example, sodium phenylphosphonate.
At the completion of the polymerization reaction, the silicone-polyimide can be isolated by diluting the reaction mixture with a material such as chloroform to reduce the solids level to about 10% and reprecipitating the resulting mixture in an organic solvent such as isopropanol.
The resulting product can thereafter be dried by convention-al means such as a vacuum oven.
The silicone-polyimides of the present invention are valuable as wire coating compositions and can be extrud ed onto metallic conductors such as aluminum or copper wire to thicknesses up to 50 mil. During the polymerization reaction, a chain-stopper, such as a monofunctional aromatic anhydride or monofunctional aromatic amine, for example, aniline or phthalic anhydride, can be used if desired to control the molecular weight of the silicone-polyimide.
In order that those skilled in the art will be better able to practice the present lnvention, the following P~-163~
~LZ~4~

examples are given by way of illustration and not by way of limitation. All parts are by weight unless otherwise speci-fied.

ExamPle 1 A series of 3-aminopropyldimethylsiloxy terminated polydimethylsiloxanes were prepared having an average of from about 8 to about 30 dimethylsiloxy units. The proce-dure for making a 3-aminopropyl terminated polydimethyl-siloxane having an average of about 9.5 dimethylsiloxy units was as follows:
A mixture of 102.52 moles of bis-(3-aminopropyl)-tetramethyldisiloxane and 230.66 moles of octamethylcyclo-tetrasiloxane and 1.0 moles of tetramethylammonium hydroxide was stirred at a temperature of about 80C for 6 to 8 hours under a nitrogen atmosphere. The equilibration was monitor-ed by gas chromatography. When the equilibration was completed, the temperature was raised to 150~C to effect catalyst decomposition and devolatilization of from 10-15%
by weight of low molecular cyclics. The mixture was aliowed to cool to room temperature and then titrated for amine end groups with standardized perchloric acid in acetic acid using methyl violet at the indicator. There was obtained a 3-aminopropyldimethylsiloxy polydimethylsiloxane having an average of about 9.5 dimethylsiloxy units and a molecular weight of about 949.13 per chain.
A silicone-polyimide was prepared in accordance with the following procedure:
A mixture of 7.502 grams of 2,2-bis[4-(3,4-dicar-boxyphenoxy)phenyl]propane dianhydride, 0.17B grams of phthalic anhydride, 0.811 grams of metaphenylenediamine, 6.173 grams of a 3-aminopropyldimethylsiloxy terminated 31 Z~ 8 polydimethylsiloxane having an average of 7.7 dimethylsilsxy units per chain, 40 ml. of orthodichlorobenzene and 0.004 gram of sodium phenylphosphinate was heated under a positive nitrogen pressure at 140C for 1 hour. Solvent and water were removed from the reaction mixture until a total of about 15 ml. of orthodichlorobenzene was collected resulting in a reaction mixture having about 30% solids. The mixture was refluxed for an additional 4 hours and then allowed to cooL. The cooled reaction mixture was diluted with 25 ml.
of chloroform and poured with vigorous stirring into 250 ml.
of isopropanol. A product was isolated by filtration and washed with copious quantities of isopropanol. The result-ing solid was dried for at least 4 hours at 120-150C in a vacuum oven. The dried solid was then redissolved in chloroform (to 15% solid) and again reprecipitated into isopropanol. There was obtained 11.4 grams for an 81% yield of a silicone-polyimide after drying in a vacuum oven.
Based on method of preparation the resulting silicone-poly-imide consisted essentially of polyimide having 42% by weight of polydimethylsiloxane blocks having an average of about 7.3 dimethylsiloxy units.
Several additional silicone polyimides were prepared from a 3-aminopropyl dimethylsiloxy terminated polydimethylsiloxane having an average of about 15 dimethyl-siloxy units. These silicone polyimides varied over a wei~ht percent range of 29-48 of chemically combined poly-dimethylsiloxane based on weight of silicone-polyimide.
Tensile elongations were determined from extruded strands obtained from dried polymer charged to a Tinius-Olsen Extrusion Plastometer heated to 275-320~C.
The results of those measurements are shown in Figure 1 and in the following table:

~D-16~64 .
12~4~

Table I
Effect of Wt% Dimethylsiloxane , On Percent Elongation Wt~ Siloxane ~ Elongation 10 The above results show that percent elongation is dependent on the weight percent of diorganosiloxane in silicone-polyimide.

Example 2 The procedure of Example 1 was repeated to provide : 15 several silicone-polyimides with polydimethylsiloxane blocks having from about 8-30 chemically combined dimethylsiloxy units. The silicone-polyimides were evaluated for elonga-tion and flammability in accordance with UL-94 as shown in Figure 2 and the following table:

Table II
Flammability and Percent Elongation of Silicone-Polyimide SiloxaneWt% UL-94 BlockDiorgano- Flame Out*
25 LengthSiloxane% Elongatio~ Time (sec) 9.5 37 200 21 57 200 '50 sec ~Flame out time (FOT) average for 10 ignitions RD-1~364 ~'~7~69~
.

The above results show that silicone-polyimide wire coating compositions having an average block length of from about 8 to about 20 dimethylsiloxy units, can provide a percent elsngation of at least 150%, while satisfying the V-O requirements of less than 50 seconds FOT for an average of 10 ignitions. An average block length of about 30 required too much chemically combined methylsiloxane to achieve a satisfactory degree of elongation which rendered it flammable.

Example 3 In accordance with the procedure of Thames et al, Journal of Organic Chemistry, A. Org. Chem. 1975, 40, 1090, there was prepared 3-bromo-N,N~bis(trimethylsilyl)aniline.
There was added 2.6 moles of butyl lithium in hexane over a 15 minute period to a mixture of 50 grams of the 3 bromo-N,N-bis(trimethylsilyl)aniline in 400 ml. of anhydrous ether cooled to 0C under a nitrogen atmosphere.
The resulting reaction mixture was allowed to stir for an additional 2 hours at 0~C. The mixture was then added to a mixture of 100 ml. of anhydrous ether and 16.06 grams of 1,3-dichloro-1,1,3,3-tetramethyldisiloxane at 0C. After the solution was filtered and the solvents were removed under reduced pressure, there was obtained a 77% yield of 1,3-bis[N,N-bis(trimethylsilyl)-3-aminophenyl]-1,1,3,3-tetr-amethyldisiloxane in the form of a pale-yellow oil having a boiling point of about 169-174C.
A mixture of 38 grams of the above-bis-substituted trimethylsilylaminophenyltetramethyldisiloxane, 30 grams of methanol, 100 milligrams of p-toluene sulfonic acid monohy-drate and 300 ml. of anhydrous ether was stirred for 12 hours at room temperature. The resulting etherial solution -1~-~27~ RD-16364 was washed with two 100 ml. portions of a saturated sodium bicarbonate solution and then with 100 ml. of brine. The organic phase was dried over anhydrous magnesium sulfate, filtered and the solvents were removed under reduced pres-sure. There was obtained a 90% yield of a pale-yellow oil after vacuum distillation of the crude product which had a boiling point of 169-174C. Based on method of preparation and NMR spectra, the product was 1,3-bis(m-aminophenyl)-1,1,3,3-tetramethyldisiloxane.
A mixture of 4.8 grams of the above 1,3-bis(m-aminophenyl)-1,1,3,3-tetramethyldisiloxane, 22.48 grams of octamethylcyclotetrasiloxane and 30 milligrams of powdered potassium hydroxide was heated at 150~C for 12 hours under a nitrogen atmosphere. The temperature was lowered to 120C
and 68 milligrams of sodium bicarbonate was added. The reaction mixture was stirred for 1 hour at 120C and then cooled to 90C. The reaction mixture was diluted with 100 ml. of toluene. After an additional heating for 30 minutes at 90~C, the solution was cooled to room temperature and filtered. There was obtained a yellow oil. Based on method of preparation, IR spectra and NMR spectra the resulting product was a polysiloxanediamine. Based on the average molecular weight of the isolated material (20.6 grams determined by titration) the average length of the poly-siloxane was found to be sufficient to provide a value of n of about 19-21.
A mixture of 16.84 grams of the above aminophenyl terminated polydimethylsiloxane and 4.636 grams of 2,2-bis-[4-(3,4-dicarboxyphenoxy)phenyl]propane dianhydride dis-solved in 40 ml. of orthodichlorobenzene along with 0.0012 yram of sodium phenylphosphinate. The resulting reaction mixture was heated for 1.5 hours at 140C and then brought to reflux. Water was removed over a 2 hour period and then 1~74~

the mixture was refluxed for an additional 18 hours. A
material was isolated by diluting the polymerization reac-tion mixture with chloroform to reduce the solids level to 10%. A product was obtained by reprecipitating the result-ing solids in isopropanol. There was obtained a polymerwhich was dried in a vacuum oven at 210C for 18 hours. The product was a rubbery-like light-brown material having a glass transition temperature below room temperature and an IV of 1.4.

Example 4 The procedure of Example 3 was repeated, except that m-phenylenediamine was also used in the polymerization mixture. There was utilized 1.5674 grams of m-phenylenedia-mine, 8.1222 grams of the abo~e aminophenyl terminated polydimethylsiloxane, 10.032 grams of the aromatic bis(ether anhydride), 0.0034 grams of sodium phenylphosphinate and 40 ml. of orthodichlorobenzene. The resulting product was less flexible than the silicone-polyetherimide containing the silicone blocks having an average value of 19-21 dimethyl-siloxy units. It exhibited a glass transition temperature at about 184C. However, it had significantly superior flexibility as compared to polyetherimide resin resulting from the polymerization of m-phenylenediamine and the aromatic bis(ether anhydride) free of the aminophenyl terminated siloxane.

Exam~le 5 The procedure of Example 3 was repeated to make a variety of silicone-polyimides. Some of the silicone-poly-imides were based on the use of polydimethylsiloxane having ~7~ RD-l53~4 terminal aminophenyldimethylsiloxy units, while other silicone-polyimides were based on the use of polydimethyl-siloxane having terminal aminopropyldimethylsiloxy units.
In addition, the aminoorgano terminated polydimethylsiloxane was used in the form of a disiloxane and a polydimethylsi-loxane having about 20 chemically combined dimethylsiloxy units. A further silicone-polyimide was made utilizing aromatic bis(ether anhydride) in accordance with Example 3 and difunctional amine material consistiny of a mixture o~
equal molar amounts of m-phenylenediamine and aminopropyl-dimethylsiloxy terminated polydimethylsiloxane having about 20 chemically combined dimethylsiloxy units.
The above silicone-polyimides were then evaluated for thermal stability utilizing TGA analysis. The following results were obtained heating the respective silicone-poly-imides in air at a heating rate of 10C/min. to determine the temperature at which a 5% weight loss and 10% weight loss were experienced, where ArSi(2) indicates the phenyl substituted disiloxane containing silicone-polyetherimide and ArSi(20) indicates the phenyl terminated polydimethyl-siloxane containing silicone-polyetherimide, while GAPSi(2) indicates the aminopropyldisiloxane containing silicone-polyetherimide and GAPSi(20) indicates the aminopropyldi-methylsiloxane containing silicone-polyetherimide:
Table III
Wt. Loss in Air (~C) Silicone-~ol~etherimide ArSi(2) 490 520 GAPSi(2) 463 470 ArSi(20) 430 4A5 GAPSi(20) 390 405 It was further found that the silicone-polyimide having chemically combined m-phenylene units experienced a ~D-1~364 ~74~

5% weight loss at 395 and a 10% weight loss at 410. This data indicates that the silicone-polyimides obtained from the use of aminophenyl terminated polydimethylsiloxane ha~e significantly higher oxidative stability than the silicone-polyimides derived from the use of aminopropyl terminatedpolydimethylsiloxane. In addition, the use of m-phenylene-diamine in combination with aminopropyl terminated polydi-methylsiloxane ~as found to enhance the oxidative stability of the resulting silicone-polyimide.

ExamPle 6 An additional evaluation of the flexibility of the silicone-polyetherimides of the present invention were made having polydimethylsiloxane blocks of about 17 chemically combined dimethylsiloxy units based on the use of aminopro-pyldimethylsiloxy terminated polydimethylsiloxane. The fol-lowing results were obtained, where "n" is the number of dimethylsiloxy units in the silicone block, "Mol ~" indi-cates the moles of dimethylsiloxy units in the silicone-polyetherimide based on total moles of chemically combined units, "MW" is the molecular weight of the silicone-poly-etherimide and "Flex Mod" is the flexural modulus of the silicone-polyetherimide:
Table IV
n Mol~ MW Flex Mod 25 17 5~ 97,200 22,000 17 20 71,000 59,000 17 15 65,000 150,000 17 10 59,200 250,000 The above results show that mole percent of silicone diamine relative to the total moles of diamine used 12'~

in making the silicone-polyimide and molecular weight can influence the flexural modulus.
Although the above examples are directed to only a .few of the very many variables which can be u~ed in the practice of the present invention to make the silicone-poly-imide wire coating compositions, it should be understood that the present invention is directed to a much broader variety of aminoorganosiloxanes as shown by formula (1) and organic dianhydride as illustrated by formula (4) where R
can be further defin~d as a divalent C(6 20) aromatic - organic radical which are shown in the description preceding these examples.

Claims (10)

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:
1. Extrudable, flame retardant, polydiorganosiloxane polyimide comprising by weight, (A) from about 40 to 90% of chemically combined aryletherimide units having the formula, and (B) from about 10 to 60% of chemically combined polydiorganosiloxane consisting essentially of from about 11 to about 20 diorganosiloxy units, where the organo radicals attached to silicon are selected from monovalent C(1-4) hydrocarbon radicals and substituted monovalent C(1-14) hydrocarbon radicals, R2 is selected from the class consisting of the same or different C(1-14) divalent hydrocarbon radicals, or substituted C(1-14) divalent hydrocarbon radicals, and R4 is a divalent aryl radical selected from the class consisting of
1. Claim 1 continued:
   
   X1 is a member selected from the class consisting of -CyH2y-, ?, ?, ?, -O- and -S- , and p is 0 or 1, and y is an integer equal to 1 to 5 inclusive.
2. 2. A polydiorganosiloxane-polyimide composition in accordance with claim 1 where the polydiorganosiloxane is polydimethylsiloxane.
3. 3. A polydiorganosiloxane-polyimide composition in accordance with claim 1 having an elongation percent of greater than 100.
4. 4. A polydiorganosiloxane-polyimide in accordance with claim 1 having about 25% to 45% by weight of polydiorganosiloxane.
5. 5. A polydiorganosiloxane-polyimide composition in accordance with claim 1 consisting essentially of bisphenol A etherimide units chemically combined with a mixture of dimethylsiloxane and metaphenylene units.
6. 6. A polydiorganosiloxane-polyimide composition in accordance with claim 1 where the polydiorganosiloxane is an alkylene terminated polydiorganosiloxane.
7. I 7. Extrudable flame retardant silicone-polyetherimide wire coating compositions having an elongation of at least 100% which satisfies the UL 94 V-O test.
8. 8. Extrudable polydiorganosiloxane-polyimide in accordance with claim 1 wherein the polydiorganosiloxane block is a polydimethylsiloxane having an average of about 11 to 20 chemically combined dimethylsiloxy units.
9. 9. Extrudable polydiorganosiloxane-polyimide in accordance with claim 1 where the aryletherimide units have the formula and the polydiorganosiloxane is a polydimethylsiloxane having an average of about 11 to about 20 chemically combined dimethylsiloxy units.
10. 10. Extrudable polydiorganosiloxane-polyimide in accordance with claim 1 having about 25%
    to 45% by weight of polydiorganosiloxane.