AU612856B2 – Particulate material comprising a platinum-containing hydrosilylation catalyst and a silicone resin
– Google Patents
AU612856B2 – Particulate material comprising a platinum-containing hydrosilylation catalyst and a silicone resin
– Google Patents
Particulate material comprising a platinum-containing hydrosilylation catalyst and a silicone resin
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Publication number
AU612856B2
AU612856B2
AU36717/89A
AU3671789A
AU612856B2
AU 612856 B2
AU612856 B2
AU 612856B2
AU 36717/89 A
AU36717/89 A
AU 36717/89A
AU 3671789 A
AU3671789 A
AU 3671789A
AU 612856 B2
AU612856 B2
AU 612856B2
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AU
Australia
Prior art keywords
catalyst
particulate
platinum
silicone resin
composition
Prior art date
1988-06-23
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AU36717/89A
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AU3671789A
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Inventor
Toshio Saruyama
Atsushi Togashi
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DuPont Toray Specialty Materials KK
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Toray Silicone Co Ltd
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1988-06-23
Filing date
1989-06-22
Publication date
1991-07-18
1989-06-22
Application filed by Toray Silicone Co Ltd
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Toray Silicone Co Ltd
1990-01-04
Publication of AU3671789A
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patent/AU3671789A/en
1991-07-18
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1991-07-18
Publication of AU612856B2
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patent/AU612856B2/en
2009-06-22
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Classifications
C—CHEMISTRY; METALLURGY
C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
C08J3/00—Processes of treating or compounding macromolecular substances
C08J3/12—Powdering or granulating
C08J3/16—Powdering or granulating by coagulating dispersions
C—CHEMISTRY; METALLURGY
C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
C08J3/00—Processes of treating or compounding macromolecular substances
C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
C08J3/03—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
C08J3/07—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media from polymer solutions
C—CHEMISTRY; METALLURGY
C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
C08K9/00—Use of pretreated ingredients
C08K9/10—Encapsulated ingredients
C—CHEMISTRY; METALLURGY
C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
C08L83/04—Polysiloxanes
C—CHEMISTRY; METALLURGY
C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
C08G77/04—Polysiloxanes
C08G77/12—Polysiloxanes containing silicon bound to hydrogen
C—CHEMISTRY; METALLURGY
C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
C08G77/04—Polysiloxanes
C08G77/20—Polysiloxanes containing silicon bound to unsaturated aliphatic groups
C—CHEMISTRY; METALLURGY
C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
C08G77/70—Siloxanes defined by use of the MDTQ nomenclature
C—CHEMISTRY; METALLURGY
C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
C08J2383/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon only; Derivatives of such polymers
C08J2383/04—Polysiloxanes
Description
1 6PATENTS COMMONWEALTH OFAUSTRALIA PTNSACT 1952-69 COMPLETE SPECIFICAT ION
(ORIGINAL)
Class Application Number: Lodged: Form Int. Class Complete Specification Lodged: 0 Accepted: 0 Published: 00 00 0 0~aedAt 0* N3me of Applicant: TORAY SILICONE COMPANY, LIMITED Address of Applicant: 3-16, 2-chorne, Nibonbashi-Murornachi, Chuo–Ku, Tokyo, Japan 0 a’ 0 Acttial Inventor: 0 t Address for Service: ATASUSHI TOGASHI, TOSHIO SARUYAMA XK0=CVT=W,!ra ateruark Patent Tradzemark Attorneys 50 QUEEN STREET, MELBOURNE, AUSTRALIA, 3000, Complete Specification for the invention entitled: PARTICULATE MATERIAL COMPRISING A PLATINUM-CONTAINING HYDROSILYLATION CATALYST AND A SILICONE RESIN The following statement Is a full description of this Invenltion, Including the best method of perfowming it. known to’ us
I
PARTICULATE MATERIAL COMPRISING A PLATINUM-CONTAINING HYDROSILYLATION CATALYST AND A SILICONE RESIN The present invention relates to a composition in particulate form comprising a platinum-containing hydrosilylation reaction catalyst. More particularly, the present invention relates to a particulate form of a platinum-containing hydrosilylation catalyst that will not cause premature curing when incorporated into 0 organopolysiloxane compositions which cure by a o hydrosilylation reaction.
0 One objective of the present invention is to 00 provide a platinum-type hydrosilylation catalyst in 0 00 particulate form. When used as the curing catalyst in a hydrosilylation-curing organopolysiloxane composition, this catalyst composition provides an excellent storage stability while inducing a rapid curing upon heating. A second objective is to provide a relatively simple method for the preparation cf said particulate.
In accordance with the present invention a 0 0, particulate composition comprising a platinum-containing hydrosilylation catalyst and a silicone resin having a softening point of from 50 to 200° C. is washed with a liquid that is a solvent for the catalyst but not for the resin. The average size of the particulate does not exceed 100 micrometers.
This invention provides an improved particulate composition comprising a platinum-containing hydrosilylation reaction catalyst dispersed in a solid silicone resin having a softening point within the temperature range of from 50 to 200 degrees Centigrade.
The improvement comprises an average particle diameter 2 for said particulate not exceeding 100 micrometers and the essential absence of said catalyst in the surface layer of said particulate.
The characterizing features of the present catalyst composition are 1) an average particle size of less than 100 microns, and 2) the substantial absence of catalyst in the surface layer of the particulate material. The latter is achieved by washing the particulate material in a liquid that is a solvent for the catalyst but not for the resin.
The silicone resin used in the present compositions must have a softening point in the range of from 50 to 200 degrees Centigrade. A softening point below 50 degrees Centigrade will result in a substantial reduction in storage stability after addition to the hydrosilylation-curing organopolysiloxane composition.
At softening points in excess of 200 degrees Centigrade, the minimum temperature e’t which catalytic activity appears becomes too high, and the function as a catalyst is essentially not realized. Viewed from these standpoints, the softening temperature of the silicone resin is preferably from 70 to 150 degrees Centigradei The molecular and chemical structure of the silicone resin are not particularly crucial. However, it ‘2 is essential that this resin not be permeable with respect to the platinum-containing hydrosilylation catalyst. Furthermore, when used as a curing catalyst for organopolysiloxane compositions that cure by a hydrosilylation reaction, it is also essential that the silicone resin be insoluble in the organopolysiloxane ingredients of the composition to which the present catalyst composition is added.
4 I I–~-~raa 3 Suitable silicone resins include but are not limited to those of the following average unit formula RaSiO(4-a)/2 where R represents a methyl radical, a phenyl radical or mixtures thereof and the value of a is from 0.8 to 1.8.
Examples of platinum-containing hydrosilylation reaction catalysts suitable for use in the present compositions include but are not limited to metals from the platinum group of the periodic table, compounds of *o these metals, and compositions based on these metals and compounds. It should be understood that other metals from 04 40 the platinum group of the periodic table, such as 00 palladium and rhodium, can be substituted for platinum.
0 Specific examples of platinum-containing hydrosilylation o’ 0. reaction catalysts are finely divided platinum, chloroplatinic acid, alcohol-modified chloroplatinic acid, platinum/diketone complexes, platinum/olefin complexes, chloroplatinic acid/alkenylsiloxane complexes, and any of these catalysts supported on a carrier such as alumina, silica, carbon black, and the S like. Among these, platinum/olefin complexes and chloroplatinic acid/alkenylsiloxane complexes are preferred for their high catalytic activity as hydrosilylation reaction catalysts. The platinum/alkenylsiloxane complexes described in Japanese Patent Publication Number 42-22924 [22,924/67] are particularly preferred.
It is essential that the average diameter of the particles in the present compositions not exceed 100 micrometers in order for the catalytic activity to develop satisfactorily and in order to maintain a stable dispersion in the presence of the curable organopolysiloxane compositions.
4 The concentration of catalyst in the present compositions is preferably equivalent to a platinum concentration of from 0.01 to 5 weight%.
The structure of the particulate material that constitutes the present composition is characterized by a silicone resin/catalyst mixture encapsulated by a layer of silicone resin which is essentially free of catalyst.
As a consequence of this structure, organopolysiloxane compositions curable by a hydrosilylation reaction which contain the present catalyst compositions display excellent storage stability.
In accordance with the present method for preparing catalyst compositions, parcicles having diameters not exceeding 100 micrometers and comprising a 4o mixture of a silicone resin having a softening point of from 50 to 2000 C. and a platinum-containing hydrosilylation catalyst are washed with a liquid which 01 44 is a solvent for the platinum-containing hydrosilylation o reaction catalyst and a non-solvent for said silicone resin 4 1 The procedure used to prepare the mixture of silicone resin with softening point of from 50 to 2000 C, and the platinum-containing hydrosilylation catalyst is o not particularly critical. Any of the methods known in the art can be used, so long as the average diameter of the resultant particles does not exceed 100 micrometers, These methods include mixing a silicone resin and platinum-type hydrosilylation catalyst on a hot roll as disclosed in Laid Open Japanese Patent Application Number 49-134786, and the method disclosed in United States Patent No. 4,481,341. ,n accordance with the latter method, silicone resin and a p tinum containing
M
I hydrosilylation reaction catalyst are dissolved in a co-solvent, and this co-solvent is subsequently removed by evaporation. Procedures for preparing a particulate from such mixtures include but are not limited to grinding and pulverization of solid mixtures using mechanical means as well as methods in which a solution of the mixture is introduced into spray drier.
A preferred method for preparing the present compositions comprises the following process o process and process 0 0 0 000000 0 0 preparing a solution of a platinum-containing °o0 hydrosilylLtion reaction catalyst and silicone resin 0 0 with a softening point in the temperature range of 0 50 to 200 degrees Centigrade by dissolving said silicone resin and the catalyst in water-immiscible liquid in which the silicone resin and the P00 platinum-containing catalyst are both soluble, and o0″ then preparing by adding the solution to surfactant-containing water while stirring or shaking the 0 4I 0o.0. water.
Evaporating the water-immiscible liquid from the aqueous 0 d2spersion at i temperature below the softening point of the silicone resin to obtain an aqueous dispersion of a particulate comprising the silicone resin and the platinum-containing hydrosilylation reaction catalyst, and then separating the particulate material from the aqueous dispersion.
Washing the peticulate with a liquid in which said particulate is washed with a liquid in which the platinum-containing hydrosilylation catalyst is soluble and in which said silicone resin is not insoluble.
i- I spraaaau= To explain the preceding method steps in greater detail, in process a homogeneous solution of silicone resin and platinum-containing hydrosilylation reaction catalyst is dispersed in microparticulate form in wafer to prepare an aqueous or water-based dispersion. The solvent used here should homogeneously dissolve both the silicone resin and the catalyst, and must also be immiscible with water. Furthermore, in order to facilitate removal of the solvent in process it is preferred that the boiling point of this solvent at atmospheric pressure not exceed 100 degrees Centigrade, and it is particularly preferred that its boiling point be from 30 to 70 degrees Centigrade.
Suitable solvents for process include but are not limited to methylene chloride, chloroform, tetrahydrofuran, and diethyl ether. The surfactant used here is not particularly crucial as long as it has the ability to generate a water-based dispersion, in emulsion or suspension form, of the solution of silicone resin and platinum-type hydrosilylation reaction catalyst.
o However, surfactants containing atoms such as sulfur and phosphorus which can cause a loss in the activity of the platinum-containing hydrosilylation reaction catalyst should not be used. Suitable surfactants are exemplified by water-soluble polymeric organic compounds such as partially hydrolyzed polyvinyl alcohol, In process the particulate formed in the water-based solvent dispersion generated by process (A) is separated and recovered. This particulate consists essentially of the silicone resin and platinum-containing hydrosilylation catalyst. Evaporative removal of the solvent from the recovered particulate material must be conducted at a temperature below the softening point of the silicone resin in order to avoid damage to the shape of the particulate. Evaporative solvent removal can be efficiently carried out, for example, by injecting an inert gas nitrogen, etc.) into the water-based solvent dispersion at ambient or reduced pressure.
Separation of the particulate from the water can be carried out by filtration or centrifugal separation.
In process the surface of the particulate obtained by process steps and is washed with a solvent in order to wash out and remove the platinum-containing hydrosilylation reaction catalyst present in the surface layer of the particulate. This washing solvent must be capable of dissolving the hydrosilylation reaction catalyst while at the same time not dissolving the silicone resin. Selection of a washing solvent is based on the type of platinum-containing hydrosilylation reaction catalyst and silicone resin actually used. One type of washing solvent S is an alcohol, particularly methyl alcohol or ethyl S, alcohol, Low molecular-weight organopolysiloxanes are very suitable when a platinum/alkenylsiloxane complex 0 0a catalyst is used as the hydrosilylation reaction catalyst. Among these, siloxane oligomers such as hexamethyldisiloxane and cyclic siloxanes such as octamethylcyclotetrasiloxane are particularly preferred.
The purpose of the washing step can be satisfactorily achieved simply by dispersing the particulate comprising silicone resin and platinum-containing hydrosilylation reaction catalyst in a large quantity of the washing solvent with stirring, following which the washing solvent is removed by filtration.
r -~1 The efficiency of the stirring operation can be boosted using, for example, ultrasound and other known techniques, so long as these techniques do not cause a deterioration in the platinum-containing hydrosilylation reaction catalyst or silicone resin. It is recommended that the wash temperature not exceed degrees Centigrade.
Evaporation of the residual washing solvent remaining following the filtration step yields a particulace catalyst composition of this invention.
The particulate platinum-containing hydrosilylation catalyst obtained using the preferred method of this invention has a structure in which a mixture of silicone resin and a platinum-containing hydrosilylation reaction catalyst is encapsulated by a layer of silicone resin having a softening point of from to 200 degrees Centigrade and which is essentially free of catalyst. The particulate does not exhibit catalytic activity with respect to hydrosilylation reactions at room temperature because the platinum-containing catalyst cannot leak to the surface at these temperatures. catalytic activity is exhibited at temperatures above the silicone resin’s softening point because the catalyst is able to bleed out of the particulate. Accordingly, the particulate composition of this invention is an extremely effective curing agent or curing promoter for single-package curable organopolysiloxane compositions which must have long-term storage stability at room temperature.
As an example, a thermosetting organopolysiloxane exhibiting an excellent storage stability is obtained by the addition of the particulate catalyst composition of this invention to a mixture comprising a diorganopolysiloxane having at least two alkenyl radicals in each molecule and an amount of an organohydrogenpolysiloxane sufficient to crosslink the diorganopolysiloxane. The particulate composition of the present invention is also effective as a curing agent for polyether compositions comprising an organohydrogenpolysiloxane and a vinyl-terminated polyether.
The present invention is illustrated using the following examples. In the examples, the reported viscosity values are measured at 25 degrees Centigrade, Sand cp centipoise.
o .#4 Reference Example 1 Preparation of a platinum/vinylsiloxane complex catalyst 160 g of 1,3-divinyltetramethyldisiloxane and j 32 g of chloroplatinic acid (H 2 PtC1 6H 2 0) were mixed and then blended with heating to 120 degrees Centigrade for 1 hour under a nitrogen current. A oa» platinum/vinylsiloxane complex catalyst was obtained by removing the platinum black by-product by filtration and then removing the acid with a water wash, The platinum «o metal concentration in this catalyst was 4.25 weight%.
00 4 4 00 Example 1 16,0 g silicone resin exhibiting a softening point of 110 degrees Centigrade and consisting essentially of diphenylsiloxane units, dimethylsiloxane units, and phenylsiloxane units in a 12:21:67 molar ratio, respectively, and 2.0 g of the platinumn/vinylsiloxane complex catalyst prepared as described in Reference Example 1 were dissolved in 330 g -1 I 1 i.
of methylene chloride. This methylene chloride solution was added to water containing 15 g of polyvinyl alcohol (Gosenol GL-05 from Nippon Gosei Kagaku Kogyo Kabushiki Kaisha) while stirring the water in order to prepare a water-based dispersion of the methylene chloride solution. The entire quantity of methylene chloride was then evaporated off by bubbling nitrogen gas into this aqueous dispersion at 25 to 40 degreea Centigrade over 48 hours, thus yielding a suspension comprising a microfine solid dispersed in water. This suspension was placed in a centrifugal separator and the microfine solid was separated, Analysis of the obtained microfine solid revealed it to be a particulate with an average particle size of 7 micrometers containing 0,27 weight% platinum metal, 10 g of this powder was washed once with water and was then placed in approximately 500 g methyl alcohol and washed with stirring. Analysis of the particulate after washing showed it to be a powder with an average particle size of 7 micrometers containing 0.26 weight% platinum metal.
The properties of this particulate as a hydrosilylation reaction catalyst were investigated.
A hydrosilylation-curing organopolysilQxane composition was prepared as follows: 100 g of a dimethylvinylstloxy-terminated polydimethylsiloxane having a viscosity of 1,500 centistokes (1.5×10-123 m2/sec.) at 25 degrees Centigrade, and 20 g fumed silica having a specific surface area of 200 m 2 /g and which had been previously hydrophobicized with hexamethyldisilazane were mixed. This was followed by the addition with mixing to homogeneity of 2.8 g of a inethylhydrogenpolysiloxane represented by the average molecular formula Me 3 SiO(Me 2 SiO) 3 (MeHSiO) 5 SiMe 3 0.21 g of the particulate prepared as described in the first section of this example was then added to 100 g of the initial organopolysiloxane composition with mixing to homogeneity. The storage stability and thermal curing properties of the obtained curable organopolysiloxane composition were measured, and the obtained results are reported in Table 1, The following properties of the resultant composition were determined using a Curastometer (Model 3) from the Toyo Baldwin Company as indicators of the thermal curing properties: the time until initiation of curing of the organopolysiloxane composition at 130 degrees Centigrade (1t) and the time to achieve 90% of the maximum torque value (T 90 Storage stability was evaluated by allowing the organopolysiloxane composition to stand for 90 days at degrees Centigrade, and determining the change in S viscosity during this time period. For comparison an S organopolysiloxane composition was prepared as described in the first portion of this example, but using 4) tho platinum/alkenylsiloxane complex catalyst obtaiijc Reference Example 1 or b) the powder described in the present example 1 prior to the methyl alcohol wash in place of the methyl alcohol-washed powder. The concentration of platinum metal in both of the comparative compositions was the same as that of the composition containing tho methyl alcohol-washed powder.
The curing properties and storage stability of these comparison compositions were also measured, and the results are reported in Table 1 as Comparisoni Example 1 and Comparison Example 2, respectively.
TABLE 1 Example 1 .Comparis on Example 1 Comparison Example 2 Type of Catalyst powder after methyl. alcohol wash Pt! alkenylsiloxane complex catalyst powder before methyl alcohol wash Properties curing properties I t (seconds)
T
90 (seconds) 15 240 240 storage stability viscosity immediately 3300 cp after preparation tcentxpoise) 3300 cp 3300 cp viscosity after days (centipoise) 5500 cp not measurable (gelled after minutes) 5 measurable (gelled after days) 13 Example 2 16.- g of the silicone resin described in Example 1 and 12,0 g of the placinum/vinylsiloxane complex catalyst prepared as described in Reference Example I were dissolved in 330 g of methylene chloride.
Solid flakes were recovered by the gradual removal of the methylene chloride hy injecting nitrogen gas into this methylene chloride solution with stirring. This solid was then ground and filtered through a 150 mesh filter to give a powder with an average particle size of micrometers. This particulate contained 0.42 weight% platinum metal. It was then washed with methyl alcohol according to the procedure outlined in Example I to yield a powder (IT) having an average particle size of micrometers and containing 0.40 weight% platinum metal.
A curable organopolysiloxane composition was prepared by the addition, with mixing to homogeneity, of 0.21 g of powder II to 100 g of the hydrosilylation-curable organopolysiloxane composition prepared as described in Example 1. The storage stability ,,nd thermal curing properties of this curable organopolysiloxane composition were determined using the methods described in Example 1, and these results are reported in Table 2. The only change from the evaluation procedure described in Exanple I is that the viscosity was measured after 60 days rather than after days. For comparative purposes the same curable organopolysiloxarte composition was prepared using powder I in place of methyl alcohol-washed powder I1. The amount of the powder II was equivalent to the same platinum metal content present in the compoqition containing powder II. The storage stability and thermal curing properties of the resultant curable organopolysiloxane composition were also measured, and the results are reported in Table 2 as Comparison 1xnmnle 3, h» sx TABLE 2 Example 2 Comparison Example 3 type of catalyst powder after methyl alcohol wash powder before methyl alcohol wash property curing properties I (seconds)
T
90 (seconds) storage stability viscosity immediately after preparation 18 260 18 260 3300 cp 5000 cp 3300 cp viscosity after days could not be measured (gelled after 2 days) 1 -7-P~IT n I Ir
TI
Example 3 A catalyst composition was prepared by dissolving 16.0 g of a silicone resin exhibiting a softening point of 110 degrees Centigrade and consisting essentially of diphenylsiloxane units, dimethylsiloxane units, and phenylsiloxane units in a 22 14 64 molar ratio, and 2.0 g of the platinum/vinylsiloxane complex catalyst prepared as described in Refererce Example 1 in 330 g methylene chloride. This methiylene chloride solution was added to water containing L5 g 0*polyvinyl alcohol (Gosenol GL-05 from Nippon Gosei Kagaku Kogyo Kabushiki Kaisha) while stirring the water in order to prepare a water-based dispersion of the methylene chloride solution. The entire quantity of methylene chloride was removed over 48 hours by injecting nitrogen gas into this aqueous dispersion while maintaining the temperature of the composition at froin to 40 degrees Centigrade, The resultant suspension of a S microfine solid dispersed in water was placed in a centrifugal separator and the microfine particulate was separated. 10 g of the separated particulate material 0* I were washed once with water and was then washed by stirring together with approximately 500 g of cy lic dimethylsiloxanes. The washed particulate was ana’yzed, i and was found to be a powder with an average particle size of 7 micrometers containing 0.20 weight% platinum metal.
The properties of this particulate as a hydrosilylation reaction catalyst were then investigated using a curable composition prepared as follows: 100 g of a dimethylvinylsiloxy-terminated polydimethylsiloxane exhibiting a viscosity of 1,500 centistokes and 20 g of fumed silice exhibiting a _li~JI ~~I specific surface area of 200 m2/g that had been previously hydrophobicized with hexamethyldisilazane were mixed, and 2.8 g methylhydrogenpolysiloxane with the average molecular formula Me3SiO(Me2SiO)3(MeHSiO)5SiMe3 was then added with mixing to homogeneity to yield a hydrosilylation-curing arganopolysiloxane composition.
0.27 g of the particulate prepared above was added, with mixing to homogeneity, to 100 g of this composition.
The storage stability and thermal curing properties of the resultant curable organopolysiloxane composition were measured as described in Example 1, and the results are reported below.
curing properties (seconds) 240 storage tability viscosity immediately after preparation (centipoise) 3300 viscosity after 0 days (cenipise) 400 vicst afe 90dy
Claims (2)
1. In a particulate composition comprising a platinum- containing hydrosilylation reaction catalyst as herein defined, dispersed in a silicone resin having a softening point within the temperature range of from 50 to 200 degrees Centigrade, said resin being impermeable with respect to said catalyst and being insoluble in organopolysiloxanes, the improvement comprising an average particle size for said particulate not exceeding 100 micrometers and the essential absence of said catalyst in the surface layer of said particulate.
2. A method for preparing a composition in particulate form comprising a platinum-containing hydrosilylation catalyst as herein defined dispersed in a silicone resin, said resin being impermeable with respect to said catalyst and being insoluble in organopolysiloxanes, said method comprising: preparing a solution comprising said catalyst, a silicone resin with a softening point of from 50 to 200 degrees Centigrade and a water-immiscible solvent; dispersing said solution in a mixture of water and a surfactant to form an aqueous dispersion while stirring or shaking said mixture; evaporating said solvent from said aqueous dispersion at a temperature below the softening point of said silicone resin to obtain an aqueous dispersion of a particulate comprising said silicone resin and said platinum-containing hydrosilylation reaction catalyst and separating said particulate from said aqueous dispersion; Disk 0102/1.13 f.–I -18- washing said particulate with a liquid in which said catalyst is soluble and said silicone resin is insoluble; and isolating said particulate from said liquid. DATED this 16th day of April, 1991. TORAY SILICONE COMPANY, LIMITED WATERMARK PATENT ATTORNEYS 2ND FLOOR «THE ATRIUM», 290 BURWOOD ROAD, HAWTHORN, VIC. 3122. AUSTRALIA t I *i I I 4, I 0 o 00 0,41 4 00O 0 44 flak 0102/. 13 £0 1
AU36717/89A
1988-06-23
1989-06-22
Particulate material comprising a platinum-containing hydrosilylation catalyst and a silicone resin
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AU612856B2
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1988-06-23
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JP2630993B2
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1988-06-23
1988-06-23
Granules containing platinum-based catalyst for hydrosilylation reaction and method for producing the same
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Particulate material comprising a platinum-containing hydrosilylation catalyst and a silicone resin
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JP2665941B2
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1988-06-29
1997-10-22
東レ・ダウコーニング・シリコーン株式会社
Granules containing platinum-based catalyst for hydrosilylation reaction
US5015691A
(en)
*
1989-05-22
1991-05-14
General Electric Company
One part heat curable organopolysiloxane compositions
JP2916179B2
(en)
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1989-11-17
1999-07-05
東レ・ダウコーニング・シリコーン株式会社
Heat-curable organopolysiloxane composition
JP3178827B2
(en)
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1990-05-31
2001-06-25
東レ・ダウコーニング・シリコーン株式会社
Heat-curable organopolysiloxane composition
JPH0436355A
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*
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Family Cites Families (2)
* Cited by examiner, † Cited by third party
Publication number
Priority date
Publication date
Assignee
Title
DE3131734A1
(en)
*
1981-08-11
1983-02-24
Bayer Ag, 5090 Leverkusen
HEAT-CURABLE ORGANOPOLYSILOXANE MIXTURES
US4874667A
(en)
*
1987-07-20
1989-10-17
Dow Corning Corporation
Microencapsulated platinum-group metals and compounds thereof
1988
1988-06-23
JP
JP15596488A
patent/JP2630993B2/en
not_active
Expired – Fee Related
1989
1989-06-22
CA
CA 603581
patent/CA1335730C/en
not_active
Expired – Fee Related
1989-06-22
DE
DE1989610735
patent/DE68910735T2/en
not_active
Expired – Fee Related
1989-06-22
EP
EP19890111335
patent/EP0347895B1/en
not_active
Expired – Lifetime
1989-06-22
AU
AU36717/89A
patent/AU612856B2/en
not_active
Ceased
Also Published As
Publication number
Publication date
CA1335730C
(en)
1995-05-30
EP0347895B1
(en)
1993-11-18
DE68910735D1
(en)
1993-12-23
DE68910735T2
(en)
1994-04-07
JP2630993B2
(en)
1997-07-16
EP0347895A2
(en)
1989-12-27
JPH024833A
(en)
1990-01-09
AU3671789A
(en)
1990-01-04
EP0347895A3
(en)
1991-01-16
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2004-01-29
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