US 5,124,423 AGrant
Process for Preparing Organosilicon Polymers
Issue Date:1992-06-23
•20 Claims
Abstract
Novel thermoset and thermoplastic organosilicon polymers, comprised substantially of alternating polycyclic hydrocarbon residues and cyclic polysiloxane or tetrahedral siloxysilane residues linked through carbon-silicon bonds, are disclosed.
Metadata
Assignee
- Hercules Incorporated
Inventor
- Raymond T. Leibfried
Application Information
Application Number:US 4615603
Filing Date:1990-01-05
Priority Date:1986-08-27
Art Unit:151
Classifications
IPC:
C08G 7704
Field of Search:
52852552452315;25;31479862222
Patent Drawings
This patent does not have any drawings.
Description
The following examples are presented to demonstrate this invention. They are not intended to be limiting.
Example 1
This example shows preparation of a novel thermoset polymer per this invention by reacting dicyclopentadiene and tetrakisdimethylsiloxysilane, with a ratio of carbon-carbon double bonds to hydrosilane groups of 1:1.
A reaction vessel was dried using an N.sub.2 flow and a heat gun (300.degree. C. pot temperature), stoppered and placed in a nitrogen flushed glove bag while hot. After equilibrating, the tube was tared on a balance, returned to the glove bag, and 0.027 g of Pt Cl.sub.2 was charged. A "dry" 1/2" magnetic stirrer was charged and the reaction vessel was capped Dicyclopentadiene (2.68 g; 0.02 mole) was charged to the reaction vessel using a 5 cc syringe. This mixture was heated at 90.degree. C. for 2 hours with stirring under slow N.sub.2 purge to allow the catalyst complex to form. The sample was cooled to 35.degree. C., tetrakisdimethylsiloxysilane (3.28 g; 0.01 mole) was charged via syringe and the reaction mixture was returned to the 90.degree. C. oil bath. After stirring for about 2 minutes, the sample foamed and darkened. The sample was further heated in the oil bath to 165.degree. C. for 3 hours during which time polymerization occurred as the sample continued to thicken. Additional heat treatments of 190.degree. C. for 1/2 hour, and 215 to 235.degree. C. for 3 hours were performed. The sample was allowed to cool and removed from the reaction vessel. The final sample was dark, rubbery and tough.
Example 2
This example shows preparation of a novel solid B stage polymer intermediate prepolymer by reacting norbornadiene and tetramethylcyclotetrasiloxane, with a ratio of carbon-carbon double bonds to hydrosilane groups of 2:1.
A mixture of 37.6 g (0.40 mole) norbornadiene, 24.0 g (1.10 mole) tetramethylcyclotetrasiloxane, and 0.0101 g (162 ppm) H.sub.2 PtCl.sub.6.6H.sub.2 O was stirred at room temperature for two days under a blanket of nitrogen. The mixture was heated to 50.degree. C. for 5 hours and 100.degree. C. for 1 hour under nitrogen. The resulting product was stripped at 75.degree. C. and 18 mm Hg to give 57.4 g (93%) of a viscous liquid. There was a slight trace of hydrosilane (Si-H, IR 2145 cm.sup.-1) left and Si.sup.29 NMR analysis was consistent with the tetra adduct of norbornadiene to tetramethylcyclotetrasiloxane. The product polymerizes to a non-melting solid upon heating to 210.degree. C. for a few minutes in air.
Example 3
This example shows preparation of a novel liquid B stage type polymer intermediate by partially reacting norbornadiene and tetrakisdimethylsiloxy silane, with a ratio of carbon-carbon double bonds to hydrosilane groups of 2:1. The resultant polymer intermediate was found to be stable for a period of greater than one year. It can be heated in the presence of air to form a solid polymer.
A mixture of 37.6 g (0.40 mole) norbornadiene, 32.8 g (0.10 mole) tetrakisdimethylsiloxysilane and 0.0100 g (142 ppm) of H.sub.2 PtCl.sub.6.6H.sub.2 O was stirred at room temperature for two days under a blanket of nitrogen. The mixture was then heated at 50.degree. C. for 5 hours and 100.degree. C. for 1 hour under a nitrogen blanket. The reaction product was stripped of unreacted monomers at 75.degree. C. and 18 mm HG and no condensate appeared overhead. The product was a low viscosity blend (70.0 g, 99% of theoretical). No Si-H appeared at 2145 cm.sup.-1 and Si.sup.29 NMR analysis was consistent with the tetra adduct of norbornadiene to tetrakisdimethylsiloxysilane. The product was still a low viscosity fluid after one year standing at room temperature. A few days after the preparation, a sample was polymerized to a non-melting solid by heating to 210.degree. C. for a few minutes.
Example 4
This example shows preparation of a film comprising a novel thermoset polymer per this invention, i.e., the reaction product of tetramethylcyclotetrasiloxane and norbornadiene, with a ratio of carbon-carbon double bonds to hydrosilane groups of 1:1.
Chloroplatinic acid (0.0030 g, 200 ppm) was charged to a reaction vessel under a nitrogen sweep. The reaction vessel was capped and 8.57 g (0.035 mole) tetramethylcyclotetrasiloxane and 6.43 g (0.070 mole) norbornadiene were charged to the sealed reaction vessel by syringe. The reaction vessel contents were blanketed under nitrogen and stirred while heating at 50.degree. C. for 2.5 hours. After two hours the initial yellow color disappeared and the viscosity of the fluid increased. After the 2.5 hours at 50.degree. C. the reaction mixture was diluted by injecting 15 ml dry xylene and filtered through #41 paper to remove insoluble black catalyst residues. The resulting polymer contained 10 to 50 ppm Pt (x-ray analysis).
Films of the filtered toluene solution fifteen mils thick were cast on glass plates with a doctor blade and the xylene was allowed to evaporate overnight. The films on the glass were heated at 100.degree. C. for 70 hours under nitrogen and then at 200.degree. C. for 4 hours. The films were immersed in water for a few hours at room temperature and they released from the glass. A visible/UV analysis showed no significant absorbance for these films from 220 to 800 nm.
Example 5
This example shows preparation of a molded, glass cloth reinforced, article comprising a novel thermoset polymer per this invention by preparing a B stage prepolymer by partially reacting dicyclopentadiene and tetramethylcyclotetrasiloxane (ratio of carbon-carbon double bonds to hydrosilane groups of 1:1), injecting the B stage prepolymer into a mold, and heating to complete polymerization.
Chloroplatinic acid (0.0101 g) was charged to a dry 750 ml reaction vessel in a N.sub.2 filled glove bag and the reaction vessel was sealed. Dry dicyclopentadiene (26.44 g, 0.2 mole) was charged by syringe. This mixture was heated at 55.degree. C. for one hour to form a dicyclopentadiene/H.sub.2 PtCl.sub.6 6H.sub.2 O catalyst complex. Dry tetramethylcyclotetrasiloxane (24.05 g, 0.10 mole) was added gradually at 56.degree. C. and an immediate exotherm took the temperature to 174.degree. C. The mixture was cooled to 64.degree. to 65.degree. C. and held there for 1.5 hour. Si.sup.29 NMR shows that the hydrosilation reaction is about 50% complete at this time. The low viscosity product was removed from the reaction vessel by syringe and injected into a teflon coated mold containing glass cloth which exactly filled the mold cavity. The resin in the mold was degassed at 60.degree. C. under a slight vacuum in a vacuum oven. The aspirator vacuum was manually controlled to keep the resin from foaming out of the mold. The mold was heated in an oven at 68.degree. C. for 18 hours and then at 140.degree. to 150.degree. C. for 3 days. The oven was cooled slowly and the mold unclamped to give a very hard, stiff 5".times.5".times.1/8" plaque. Samples were cut for rheological, tensile, and flexural property determinations and the following data were obtained:
Example 6
This example shows preparation of a novel thermoset polymer per this invention by reacting norbornadiene and tetramethylcyclotetrasiloxane with a ratio of carbon-carbon double bonds to hydrosilane groups of approximately 1:1.
A dry, N.sub.2 sparged vessel was charged with a stir bar and 0.0021 g of H.sub.2 PtCl.sub.6.6H.sub.2 O. The vessel was capped and charged with 4.47 g (0.05 mole) of norbornadiene. The resulting mixture was stirred for thirty minutes at 60.degree. C. Tetramethylcyclotetrasiloxane (5.83 g, 0 024 mole) was added and the reaction mixture gelled about three hours later. The sample was removed from the reaction vessel and cured at 150.degree. C. for 16 hours, 250.degree. C. for 2 hours and 280.degree. C. for 16 hours to give a brown, glassy solid.
Example 7
This example show preparation of a novel thermoset polymer per this invention by reacting dicyclopentadiene and methylcyclotetrasiloxane, with a ratio of carbon-carbon double bonds to hydrosilane groups of approximately 1:1.
Following the general procedure in Example 6, tetramethylcyclotetrasiloxane (18.1 g, 0.075 mole) was added to a heated (60.degree. C.) mixture of dicyclopentadiene (20.12 g, 0.152 mole) and H.sub.2 PtCl.sub.6.6H.sub.2 O (0.0076 g). The reaction mixture exothermed to 186.degree. C. 30 seconds after the tetramethylcyclotetrasiloxane addition. The reaction mixture was stirred for 16 hours at 60.degree. C., 24 hours at 70.degree. C. and 5 hours at 150.degree. C. The mixture was poured into an aluminum pan and cured for 12 hours at 200.degree. C., 2 hours at 225.degree. C., 2 hours at 250.degree. C. and 16 hours at 280.degree. C. to give a brown glassy solid.
The thermal stability of the polymers of Examples 6 and 7 are presented in the following table.
Example 8
This example show preparation of a novel molded, thermoset polymer per this invention by reacting dicyclopentadiene and methylcyclotetrasiloxane, with a ratio of carbon-carbon double bonds to hydrosilane groups of approximately 1:1.
Following the general procedure in Example 6, tetramethylcyclotetrasiloxane (49.76 g, 0.20 mole) was added to a heated (70.degree. C.) mixture of dicyclopentadiene (54.71 g, 0.414 mole) and H.sub.2 PtCl.sub.6.6H.sub.2 O (0.0209 g). Thirty seconds after the tetramethylcyclotetrasiloxane addition, the reaction mixture exothermed to 170.degree. C. The reaction mixture was stirred for 16 hours at 130.degree. C. and poured into a teflon coated mold. The sample was cured for 16 hours at 150.degree. C. to give an opaque, glassy solid.
Example 9
This example show preparation of a molded, glass cloth reinforced, article comprising a novel thermoset polymer per this invention. A B stage prepolymer was prepared by partially reacting dicyclopentadiene and tetramethyl cyclotetrasiloxane in amounts such that the ratio of carbon-carbon double bonds to hydrosilane groups was 1.1:1. Then, the B stage prepolymer was poured into a mold containing a glass cloth and was heated to complete polymerization.
Following the general procedure in Example 6, tetramethylcyclotetrasiloxane (28.6 g, 0.12 mole) was added to a heated (55.degree. C.) mixture of dicyclopentadiene (34.4 g, 0.26 mole) and H.sub.2 PtCl.sub.6.6H.sub.2 O (0.0126 g). Thirty seconds after the tetramethyl cyclotetrasiloxane addition, the reaction mixture exothermed to 184.degree. C. The reaction mixture was stirred for 2 hours at 80.degree. C. then transferred to a teflon-coated mold containing 50.9 g woven glass cloth. The sample was cured for 12 hours at 130.degree. C., 160.degree. C. for eight hours, and 180.degree. C. for 16 hours to give a opaque, glassy plaque containing 60.7 wt. % glass cloth. This plaque was further cured in a N.sub.2 flushed oven at 200.degree. C., 250.degree. C. and 310.degree. C. for 4 hours at each temperature.
Example 10
This example show preparation of a molded, opaque solid plaques comprising a novel thermoset polymer per this invention, by preparing a B stage prepolymer by partially reacting dicyclopentadiene and tetramethyl cyclotetrasiloxane (ratio of carbon-carbon double bonds to hydrosilane groups of 1:1), transferring the B stage prepolymer into a mold, and heating to complete polymerization.
Following the general procedure in Example 6, tetramethylcyclotetrasiloxane (76.36 g, 0.32 mole) was added to a heated (30.degree. C.) mixture of dicyclopentadiene (83.9 g, 0.64 mole) and H.sub.2 PtCl.sub.6.6H.sub.2 O (0.0148 g). Five minutes after this addition the reaction mixture exothermed to 193.degree. C. The reaction mixture was stirred for 1 hour at 55.degree. to 70.degree. C., transferred to teflon-coated molds and cured at 145.degree. C. for 18 hours under slight vacuum. The opaque solid plaques were further cured to 285.degree. C. in a N.sub.2 flushed oven.
The polymers of Examples 9 and 10 were further subjected to mechanical analysis to determine their glass transition temperature (Tg) and storage modulus (G') at various temperatures. Results are recorded in the following table.
The data in this table demonstrate the relative water insensitivity of the organosilicon polymers of this invention. The weight gained after 5 days in boiling water was about 0.1%.
Example 11
This example shows preparation of a novel thermoset polymer per this invention by reacting a dicyclopentadieneoligomer comprising about 58.43% dicyclopentadiene, 43.75% tricyclopentadiene and 5.05% tetracyclopentadiene (analyzed by G.C.), and tetramethylcyclotetrasiloxane (ratio of carbon-carbon double bonds to hydrosilane groups of 0.86:1).
A complex of 0.0076 g of H.sub.2 PtCl.sub.6.6H.sub.2 O and 21.71 g (0.12 mole) of the dicyclopentadiene oligomer was prepared by heating the two materials under a dry nitrogen blanket for one hour at 50.degree. C. Tetramethylcyclotetrasiloxane (16.10 g, 0.07 mole) was added to the yellow complex (complex temperature was 71.degree. C.). The reaction exothermed to 153.degree. C. in 8 seconds. The yellow solution was cooled to 30.degree. C., poured into Teflon coated slotted molds and cured at 150.degree. C./16 hours and 200.degree. C./4 hours. The 1/2".times.3".times.1/8" test pieces were removed from the mold and post cured at 100.degree. C./0.5 hours, 150.degree. C./0.5 hours, 200.degree. C./2 hours, 225.degree. C./2 hours, 250.degree. C./2 hours and 280.degree./16 hours.
Example 12
This example shows preparation of a novel polymer outside the scope of this invention by reacting norbornadiene dimer and bisdimethylsilyl ethylene both of which contain two reactive sites (ratio of carbon-carbon double bonds to hydrosilane groups of 1:1).
A complex of H.sub.2 PtCl.sub.6.6H.sub.2 O and norbornadiene dimer (pentacyclotetradeca-5,11-diene) was prepared by heating 0.0037 g of H.sub.2 PtCl.sub.6.6H.sub.2 O under a nitrogen blanket with 10.35 g (0.055 mole) of dry norbornadiene dimer for 1 hour at 55.degree. to 60.degree. C. This gives a clear yellow solution. Bisdimethylsilyl ethylene (8.16 g, 0.055 mole) was added and the resulting solution was heated to 58.degree. C. The reaction exothermed to 172.degree. C. within three minutes and the reaction mixture was highly viscous upon cooling to 53.degree. C. The mixture was poured into a slotted mold and heated overnight at 120.degree. C. then heated to 160.degree. C. for 6 hours and then at 180.degree. C. overnight. The polymer was very viscous at 180.degree. C. and at 160.degree. C. clear filaments could be drawn from the melt. The IR band for Si-H (2110 cm.sup.- 1) had essentially disappeared and the olefin double bonds at 4.6 ppm by proton NMR were barely detectable. The resulting clear, glassy, thermoplastic polymer softens at 112.degree. to 120.degree. C.
Example 13
This example shows the preparation of a molded article comprising a novel thermoset polymer per this invention, by partially reacting dicyclopentadiene and tetramethylcyclotetrasiloxane (ratio of carbon-carbon double bonds to hydrosilane groups of 1:1) to form a B stage type prepolymer, injecting the B stage prepolymer into a mold, and heating to complete polymerization.
The catalyst H.sub.2 PtCl.sub.6.6H.sub.2 O (0.0148 g) was charged to a dried 25 oz. reaction vessel and sealed. Under a nitrogen blanket 83.95 g (0.635 mole) dicyclopentadiene were charged by syringe. The catalyst and dicyclopentadiene were heated for 90 minutes at 60.degree. to 70.degree. C. giving a yellow solution which was cooled to 30.degree. C. Tetramethylcyclotetrasiloxane 76.36 g, 0.317 mole) was added and an exothermic reaction started in two minutes, eventually reaching 193.degree. C. After cooling to 55.degree. C., a sample was injected into a 5".times.5".times.1/8" teflon lined aluminum mold. The polymer was polymerized at temperatures ranging from 120.degree. to 280.degree. C. under a blanket of nitrogen. Some electrical properties of the cured polymer are given below:
A sample of the Example 14 polymer was immersed in boiling water for five days. The sample weight increased 0.1%. The dimensions of the sample (6.75, 1.30 cm, 0.32 cm) were unchanged after the boiling water treatment. The modulus/temperature curve and glass transition temperature (250.degree. C.) were also unchanged by the boiling water treatment.
Example 14
This example shows preparation of a novel thermoplastic polymer per this invention by reacting dicyclopentadiene and methylhydrocyclosiloxanes, with a ratio of carbon-carbon double bonds to hydrosilane groups of 0.5:1.
Chloroplatinic acid (0.0120g) was weighed into an 8 oz. reaction vessel under a nitrogen blanket in a dry box and the septum was sealed. Dry dicyclopentadiene (23.01 g, 0.174 mole, 0.348 gram equivalents of olefin) was injected into the reaction vessel by a hypodermic syringe The contents of the reaction vessel were heated to 60.degree. to 65.degree. C. for 1 hour, under a nitrogen blanket, and the chloroplatinic acid dissolved. Dry air was swept through the reaction vessel for 10 to 15 minutes and the contents were cooled to 31.degree. C. Methylhydrocyclosiloxanes, consisting of 54% tetramethyl cyclotetrasiloxane, 20% pentamethyl cyclopentasiloxane, 5% hexamethyl cyclohexasiloxane, 19% higher methylhydrocyclosiloxanes (up to approximately ((CH.sub.3 (H)SiO-).sub.20), and 2% linear methylhydrosiloxanes, were injected and the reaction exothermed to 179.degree. C. After cooling the reaction product to 60.degree. C., it was poured into a teflon coated stainless steel mold. The mold was placed into a vacuum oven and a vacuum applied (approximately 15 mm Hg pressure, vacuum pump) for 10 to 15 minutes. Then, the mold was heated under nitrogen for 15 hours at 130.degree. C., for 6 hours at 160.degree. C., for 16 hours at 180.degree. C., for 4 hours at 200.degree. C., and for 4 hours at 225.degree. C. Attempts to obtain thermoset behavior were then abandoned. The final product was extremely viscous at room temperature
The final product can be blended with a mixture having a ratio of carbon-carbon double bonds to hydrosilane groups of, e.g, 1.5:1 to 1.75:1 to form a composition with thermoplastic behavior and then heated to 150.degree. to 285.degree. C. to form a thermoset polymer. For instance, the polymer of example 21 and this polymer might be heated to 130.degree. to 140.degree. C., mixed in equal amounts, and cooled to form a thermoplastic blend that can be cured upon further heating (approximately 150.degree. to 285.degree. C.).
Example 15
This example shows preparation of a novel thermoset polymer per this invention, by reacting dicyclopentadiene and methylhydrocyclosiloxanes in the same manner as in example 14, except that the monomers were used in amounts such that the ratio of carbon-carbon double bonds to hydrosilane groups was 0.7:1 and the final heating was for 6 hours at 180.degree. C., for 6 hours at 225.degree. C., for 2 hours at 235.degree. C., and for 4 hours at 285.degree. C.
The polymer of this example exhibits thermoset behavior when polymerized at 225.degree. C. The polymer does not have a melting point, but softens at 100.degree. C. to a soft extendable elastomer. The polymer is a tough, leather like solid at room temperature It is flexible enough to be twisted 360.degree. before tearing.
Example 16
This example shows preparation of a novel thermoset polymer per this invention by reacting dicyclopentadiene and methylhydrocyclosiloxanes in the same manner as in example 14, except that the monomers were used in amounts such that the ratio of carbon-carbon double bonds to hydrosilane groups was 0.85:1.
The thermoset polymer formed after heating to 225.degree. C. was tougher than that found in example 16. This hard, solid polymer maintains a high modulus up to 200.degree. C. and exhibits elastomeric behavior when heated to 235.degree. C.
Example 17
This example shows preparation of a novel thermoset polymer per this invention by reacting dicyclopentadiene and methylhydrocyclosiloxanes in the same manner as in example 14, except that the monomers were used in amounts such that the ratio of carbon-carbon double bonds to hydrosilane groups of 1.15:1 and the final heating was for 4 hours at 150.degree. C., for hours at 235.degree. C., and for 4 hours at 285.degree. C.
Example 18
This example shows preparation of a novel thermoset polymer per this invention by reacting dicyclopentadiene and methylhydrocyclosiloxanes in the same manner as in example 17, except that the monomers were used in amounts such that the ratio of carbon-carbon double bonds to hydrosilane groups of 1.30:1.
All the polymers produced in examples 16 to 18 exhibited thermoset characteristics and did not melt or lose their shape at temperatures below the decomposition points of the polymers (400.degree. to 500.degree. C.). Polymers prepared from reactants having a carbon-carbon double bond:hydrosilane equivalents ratio near 1:1 were post-cured at 285.degree. to 300.degree. C. to increase their glass transition temperature to the 260.degree. to 300.degree. C. range. The crosslink density of such polymers was high enough to prevent segmental motion and network deformation.
Example 19
This example shows preparation of a novel thermoset polymer per this invention by reacting dicyclopentadiene and methylhydrocyclosiloxanes in the same manner as in example 15, except that the monomers were used in amounts such that the ratio of carbon-carbon double bonds to hydrosilane groups was 1.46:1 and the final heating was for 6 hours at 150.degree. C., for 6 hours at 200.degree. C., for 2 hours at 235.degree. C., and for 4 hours at 285.degree. C.
Example 19 demonstrates polymerization in the transition range from thermoset behavior to thermoplastic behavior. When polymerized up to 200.degree. C., the sample softened to a highly compressible elastomer at about 120+ to 125.degree. C. When the sample was post-cured at 285.degree. C., the glass transition temperature was raised to only 200.degree. C. The degree of crosslinking was limited by available hydrosilane groups.
Example 20
This example shows preparation of a novel thermoplastic polymer per this invention by reacting dicyclopentadiene and methylhydrocyclosiloxanes in the same manner as in example 14, except in amounts such that the ratio of carbon-carbon double bonds to hydrosilane groups was 1.61:1 and the final heating was for 6 hours at 150.degree. C., for 6 hours at 200.degree. C., for 8 hours at 235.degree. C., and for 4 hours at 285.degree. C.
Example 21
This example shows preparation of a novel thermoplastic polymer per this invention by reacting dicyclopentadiene and methylhydrocyclosiloxanes in amounts such that the ratio of carbon-carbon double bonds to hydrosilane groups was 1.75:1.
A catalyst solution containing 600 ppm chloroplatinic acid was prepared by heating 0.0953g of chloroplatinic acid with 158.8g dicyclopentadiene to 70.degree. C. for 1.5 hours in a sealed 8 ounce reaction vessel, under nitrogen. A 150 ppm chloroplatinic acid solution was prepared by diluting 30g of the above catalyst solution with 90g of dicyclopentadiene. A portion of the resultant chloroplatinic acid solution (7.92g) was weighed into a 7 inch reaction vessel with 4.59g of dicyclopentadiene, making a 95 ppm concentration of chloroplatinic acid in dicyclopentadiene (0.185 gram equivalent of olefin). Then, 7.21 g (0.106 hydrosilane equivalents) of methylsiloxanes (described in example 15) were injected into the sealed reaction vessel at 23.degree. C. The reaction mixture was heated to 36.degree. C. and a slight exotherm raised the temperature to 60.degree. C., where the mixture became viscous. A vacuum (15 mm Hg) was applied to the contents of the reaction vessel at 45.degree. C. for 10 minutes to pull gas out of the reaction product. The product was poured into a teflon coated stainless steel mold and heated in a nitrogen blanket for 6 hours at 150.degree. C., for 20 hours at 200.degree. C., and for 6 hours at 225 to 235.degree. C. The 3".times.1/2".times.1/8" specimens removed from the mold were transparent, hard solid with a melting point of 117.degree. to 125.degree. C. This solid could be ground into a crystalline powder.
The polymers of examples 20 and 21 do not form a complete polymeric network, even when they are polymerized at 225.degree. to 235.degree. C. They are completely thermoplastic and form a viscous, flowable liquid above their melting points. The solids can be ground into powder.
The properties of the polymers prepared in examples 14 to 21 are shown in the following Table.
Example 22
This example shows preparation of graphite fiber composite.
Chloroplatinic acid (0.0185g) was weighed into a reaction vessel in a dry box and the reaction vessel was sealed. Dicyclopentadiene (47.15g, 0.357 mole, 0.714 equivalents) was injected into the reaction vessel and the mixture was heated with stirring to 60.degree. C. for 1 hour. After cooling to 36.degree. C., tetramethylcyclotetrasiloxane (44.67g) was injected. In two minutes, the sample exothermed to 192.degree. C. The product was cooled and injected into a teflon lined mold 5".times.5".times.1/8" containing ten 5".times.5" sheets of square woven graphite fiber cloth. The loaded mold was heated in a nitrogen blanketed oven for 15 hours at 130.degree. C., for 6 hours at 160.degree. C., and for 12 hours at 180.degree. C. The resulting composite had good flexural strength (68,000 psi) and modulus (4.7.times.10.sup.6 psi).
While this invention has been described with respect to specific embodiments, it should be understood that these embodiments are not intended to be limiting and that many variations and modifications are possible without departing from the scope of this invention.
Claims
What is claimed:
1. A method of preparing a crosslinked organosilicon polymer comprised substantially of alternating polycyclic hydrocarbon residues and cyclic polysiloxane or tetrahedral siloxysilane residues linked through carbon-silicon bonds, which method consisting essentially of providing (a) a cyclic polysiloxane or tetrahedral siloxysilane containing at least two .ident.SiH groups and (b) a polycyclic polyene having at least two non-aromatic carbon-carbon double bonds in its rings, wherein the ratio of carbon-carbon double bonds in the rings of (b) to .ident.SiH groups in (a) is in the range of about 0.5:1 up to about 1.8:1 and at least one of (a) and (b) has more than two reactive sites and reacting the cyclic polysiloxane or the tetrahedral siloxysilane (a) and the polycyclic polyene (b) in the presence of a platinum-containing catalyst and subjecting said polymer to heat to drive said crosslinking to a maximum.
2. The method of claim 1 wherein the cyclic polysiloxane or tetrahedral siloxysilane containing at least two .ident.SiH groups is selected from the class consisting of: ##STR15## wherein R is hydrogen, a substituted or unsubstituted alkyl, alkoxy, aromatic or aryloxy radical, n is an integer from 3 to about 20, and R is hydrogen on at least two of the silicon atoms; and ##STR16## wherein R is as defined above and is hydrogen on at least two silicon atoms in the molecule.
3. The method of claim 2 wherein the silicon containing residue is a polyvalent residue based on a cyclic polysiloxane or a mixture of cyclic polysiloxanes.
4. The method of claim 2 wherein the silicon-containing residue is a polyvalent residue based on a tetrahedral siloxysilane or a mixture of tetrahedral siloxysilanes.
5. The method of claim 1 wherein the polycyclic hydrocarbon residue is a divalent saturated residue based on norbornadiene.
6. The method of claim 3 wherein the polycyclic hydrocarbon residue is a divalent saturated residue base on norbornadiene.
7. The method of claim 4 wherein the polycyclic hydrocarbon residue is a divalent saturated residue based on norbornadiene.
8. The method of claim 1 wherein the polycyclic hydrocarbon residue is a saturated divalent residue based on dicyclopentadiene.
9. The method of claim 3 wherein the polycyclic hydrocarbon residue is a saturated divalent residue based on dicyclopentadiene.
10. The method of claim 4 wherein the polycyclic hydrocarbon residue is a saturated divalent residue based on dicyclopentadiene.
11. The method of claim 1 wherein the polycyclic polyene is selected from the class consisting of norbornadiene, dicyclopentadiene, tricyclopentadiene, hexahydronaphthalene, dimethanohexahydronaphthalene and norbornadiene dimer.
12. The method of claim 3 wherein the polycyclic polyene is selected from the class consisting of norbornadiene, dicyclopentadiene, tricyclopentadiene, hexahydronaphthalene, dimethanohexahydronaphthalene and norbornadiene dimer.
13. The method of claim 4 wherein the polycyclic polyene is selected from the class consisting of norbornadiene, dicyclopentadiene, tricyclopentadiene, hexahydronaphthalene, dimethanohexahydronaphthalene and norbornadiene dimer.
14. The method of claim 1 wherein the ratio of carbon-carbon double bonds in (b) to .ident.SiH groups in the rings of (a) is in the range of about 0.7:1 up to about 1.3:1.
15. The method of claim 1 wherein the ratio of carbon-carbon double bonds in the rings of (b) to .ident.SiH groups in (a) is in the range of from about 0.8:1 up to about 1.1:1.
16. The method of claim 1 wherein the platinum-containing catalyst is selected from the group consisting of chloroplatinic acid, PtCl.sub.2 and dibenzonitrile platinum dichloride.
17. The method of claim 1 wherein the platinum-containing catalyst is chloroplatinic acid.
18. The method of claim 2 wherein the platinum-containing catalyst is chloroplatinic acid.
19. The method of claim 1 wherein the polymer is a thermoplastic polymer and the ratio of carbon-carbon double bonds in the rings of (B) to SiH groups in (a) is in the range of from about 0.5:1 up to about 0.7:1.
20. The method of claim 1 wherein the polymer is a thermoplastic polymer and the ratio of carbon-carbon double bonds in the rings of (b) to SiH groups in (a) is in the range of from about 1.3:1 up to about 1.8:1.
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