US 4,748,166 AGrant
RTV Storage Stable, Water-Free Organopolysiloxanes
Issue Date:1988-05-31
•15 Claims
Abstract
Storage stable, water-free, RTV organopolysiloxane adhesives curable in the presence of water or atmospheric moisture, and comprising a dihydroxydiorganopolysiloxane polymer, fillers, an amine fraction and a curing catalyst, are characterized by incorporation therein of a polyalkoxylated organosilane having the formula: wherein R' is methyl, vinyl, allyl, methallyl or phenyl, and p and x are each one or two.
Metadata
Assignee
- Rhone-Poulenc Industries
Inventors
- Alain Gautier
- Bernard Laisney
- Michel Letoffe
Application Information
Application Number:US 8698597
Filing Date:1986-05-28
Priority Date:1979-06-08
Art Unit:151
Classifications
IPC:
C08K 1100
Field of Search:
524528525860;493;497;445;448;89;262;188;186;31;13;16;437;436;431;486;432;433;435;404 ;425;702;703;730;785;786;780;789;796;588;84715;17;18;21;22;33;34104;106
Patent Drawings
This patent does not have any drawings.
Description
In order to further illustrate the present invention and the advantages thereof, the following specific examples are given, with all parts and percentages being by weight, it being understood that same are intended only as illustrative and in nowise limitative.
Example 1
70 parts of an .alpha.,.omega.-dihydroxydimethylpolysiloxane oil having a viscosity of 50,000 mPa.s at 25.degree. C., 40 parts of an .alpha.,.omega.-bis-(trimethylsiloxy)-dimethylpolysiloxane oil having a viscosity of 20 mPa.s at 25.degree. C., 3 parts of diphenylsilanediol, 15 parts of a pyrogenic silica having a specific surface area of 200 m.sup.2 /g, and 45 parts of calcium carbonate having a mean particle diameter of 5 microns were successively introduced into a malaxator.
The contents of the malaxator were triturated for 2 hours at a temperature of 120.degree. C. and under a pressure of 4,000 Pa. This resulted in the formation of an anhydrous, homogeneous paste K.sub.1 (171 parts).
The paste was permitted to cool to about 60.degree. C. and the following ingredients were incorporated therein at this temperature: 7 parts of the silane of the formula CH.sub.2 .dbd.CHSi(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3, 4 parts of the silane of the formula H.sub.2 NCH.sub.2 CH.sub.2 NH(CH.sub.2).sub.3 Si(OCH.sub.3).sub.3 and 0.1 part of a tin salt obtained by heating, at 110.degree. C. for 3 hours, a mixture consisting of 100 parts of dibutyltin dilaurate and 27 parts of butyl titanate. This combination of the two silanes and the tin salt defines a crosslinking system K.sub.2.
The mixture was then malaxated for 5 minutes at 60.degree. C. and this resulted in the formation of a homogeneous composition P.sub.1 which did not flow in the vertical position; such composition was stored in a sealed container which was impervious to moisture.
(a) One portion of this composition P.sub.1 was spread, in the open atmosphere (temperature 20.degree. C., relative humidity 50%), as a 2 mm thick layer, onto a polyethylene plate which had first been pre-coated with a commercial detergent.
After an exposure time of 30 minutes, the applied layer was non-tacky to the touch, and, after 24 hours, it had been converted into a rubbery film. When such film was seven (7) days old, it possessed the following mechanical properties:
Shore A hardness (in accordance with French Standard Specification T 51,109) =20.
Tensile strength (in accordance with French Standard Specification T 46,002) =1.5 MPa.
Elongation at break (in accordance with French Standard Specification T 46,002) =600%.
Tear strength (in accordance with French Standard Specification T 46,007) =50 N/cm.
Elongation at tear (in accordance with French Standard Specification T 46,007) =250%.
(b) Another portion of the composition P.sub.1 was utilized to manufacture test-pieces in accordance with ASA Standard Specification 116-1-1960, the method of manufacture of each test-piece being as follows:
Two square plates, having sides 50 mm in length, were placed face-to-face and 12 mm apart, the same consisting of that material, the adhesion to which of the cured elastomeric composition is to be measured. The interspace created between the two plates was then totally blocked with wooden wedges, except for the central portion of such interspace, so as to define a cavity having the dimensions 50.times.12.times.12 mm and extending from one edge of the plates to the other. This cavity was filled with the composition, the entire assembly being maintained for 28 days at ambient temperature and the wedges were then removed in order to release the test-piece, or specimen. Such specimen thus comprised two plates of the same material, which were attached to one another, along one of their median lines, by a parallelepipedic bar of elastomer.
The test-pieces manufactured in this fashion were divided into three batches of equal size and the test-pieces making up each batch differed from one another in the nature of the material forming the plates themselves, this material being selected from among glass, aluminum, concrete, fir and polyvinyl chloride (PVC).
(i) First batch: the tensile strength (TS) of the test-pieces, and also the corresponding elongation (E/B), were measured using a tensile tester actuated in accordance with the recommendations of ASA Standard Specification 116-1-1960. The results are summarized in Table 1 below.
All of the breaks were cohesive and same occurred in the bulk of the bar of elastomer; thus, there were no adhesive breaks characterized by detachment of the bar at the level of its zones of contact with the plates.
(ii) Second batch: the test-pieces were placed under tension by subjecting same to an elongation of 150% with the aid of wedges, and the condition of the testpieces was examined 24 hours after application of such tension; it was found that all of the test-pieces passed the test and that there were neither any cohesive or adhesive breaks.
(iii) Third batch: the test-pieces were immersed in water at 25.degree. C. for 96 hours; same were then placed under tension by being subjected to an elongation of 150%, and the condition of the test-pieces was examined 24 hours after the application oftension; it was again found that all of the test-pieces passed the test.
(c) A third portion of the composition P.sub.1 was introduced into aluminum tubes, each having a capacity of 100 cm.sup.3 ; such filled tubes were then closed and maintained for 48 hours in an oven heated to 100.degree. C.
After cooling the containers to about 20.degree. C., their contents were spread, as a 2 mm thick layer, on a polyethylene plate which had first been pre-coated with a commercial detergent; it was found that the deposited layer behaved in essentially the same manner as the layer described under (a), with a touch-dry time of 30 minutes and a crosslinking time of 24 hours. When it was seven (7) days old, the rubbery film formed had the following properties:
Shore A hardness =18
Tensile strength =1.1 MPa
Elongation at break =550%
Tear Strength =45 N/cm
Elongation at tear =200%
(d) A fourth portion of composition P.sub.1 was taken after a storage period of 8 months in a container impervious to moisture.
This portion was tested as described under (a); the touch-dry time of the deposited layer was found to be 25 minutes and the crosslinking time of this layer was found to be 20 hours.
The mechanical properties of the resulting film were as follows:
Shore A hardness =20
Tensile strength =1.4 MPa
Elongation at break =500%
Tear strength =55 N/cm
Elongation at tear =180%
(e) By way of comparison, 5 compositions P'.sub.1, P".sub.1, P"'.sub.1, P.sup.4.sub.1 and P.sup.5.sub.1 were prepared in accordance with the procedure employed for preparing the composition P.sub.1, except that the constituents of the crosslinking system K.sub.2 were modified in the following manner:
(i) Composition P'.sub.1 : the tin salt was not employed.
(ii) Composition P".sub.1 : the silane H.sub.2 N(CH.sub.2).sub.2 NH(CH.sub.2).sub.3 Si(OCH.sub.3) was not employed; however, in order to retain the same level of alkoxy groups, bonded to the silicon atoms, as in the composition P.sub.1, 12.2 parts of the silane CH.sub.2 .dbd.CHSi(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3 were introduced instead of 7 parts.
(iii) Composition P"'.sub.1 : the silane CH.sub.2 .dbd.CHSi(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3 was not employed; however, in order to have the same level of alkoxy groups, bonded to the silicon atoms, as in the composition P.sub.1, 9.6 parts of the silane H.sub.2 N(CH.sub.2).sub.2 NH(CH.sub.2).sub.3 Si(OCH.sub.3).sub.3 were introduced instead of 4 parts.
(iv) Composition P.sup.4.sub.1 : the 7 parts of the silane CH.sub.2 .dbd.CHSi(OCH.sub.2 CH.sub.2 OCH.sub.2).sub.3 were replaced by 5 parts of the silane Si(OC.sub.2 H.sub.5).sub.4, and the 0.1 part of the tin salt was replaced by 0.02 part of the same salt (if 0.1 part of this salt be employed the composition becomes very thick and can no longer be extruded).
(v) Composition P.sup.5.sub.1 : the 7 parts of the silane CH.sub.2 .dbd.CHSi(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3 were replaced by 4 parts of the silane CH.sub.3 Si(OC.sub.2 H.sub.5).sub.3, and the 0.1 part of the tin salt was replaced by 0.02 part of the same salt (if 0.1 part of this salt be employed, the composition can no longer be extruded).
The aforesaid compositions were next examined in accordance with the tests utilized in connection with the composition P.sub.1, and the following results were recorded: Composition P'.sub.1 : when exposed to the atmosphere in the form of a 2 mm thick layer, this composition crosslinked unsatisfactorily; thus, after an exposure time of seven (7) days, it still had not been converted into a film of elastomer which could be stripped.
Composition P".sub.1 : this composition was not storage stable in a container impervious to moisture; it solidified after a storage time of 30 hours.
Composition P"'.sub.1 : when exposed to the atmosphere in the form of a 2 mm thick layer, this composition hardened in 48 hours; however, the stripped film did not have good mechanical properties; in particular, after aging for 14 days, it possessed a Shore A hardness of 5 and a tensile strength of 0.2 MPa.
Composition P.sup.4.sub.1 : after a treatment in which it was enclosed in aluminum tubes and heated for 48 hours at 100.degree. C., this composition did not harden further; when exposed to the atmosphere, the deposited layers remained constantly pasty.
Composition P.sup.5.sub.1 : when heated as indicated above, for 48 hours at 100.degree. C., this composition hardened unsatisfactorily on subsequent exposure to the atmosphere; it was necessary to wait for fifteen (15) days in order to obtain a film of elastomer which could be stripped.
Example 2
Two compositions P.sub.2 and P.sub.3 were prepared by following the procedure employed for preparing the composition P.sub.1 described in Example 1, except that the constituents of the crosslinking system K.sub.2 were modified as follows:
Composition P.sub.2 : the 4 parts of the silane H.sub.2 N(CH.sub.2).sub.2 NH(CH.sub.2).sub.3 Si(OCH.sub.3).sub.3 were replaced by 5.5 parts of the silane H.sub.2 N(CH.sub.2).sub.2 NH(CH.sub.2).sub.3 Si(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3.
Composition P.sub.3 : the 7 parts of the silane CH.sub.2 .dbd.CHSi(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3 were replaced by 8 parts of the silane Si(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.4, and 0.05 part of the tin salt was utilized instead of 0.1 part.
(a') One portion of each of these two compositions was spread, as a 2 mm thick layer, on a polyethylene plate in accordance with the process described under (a) of Example 1.
The touch-dry time and the hardening time of the deposited layers, and also the characteristics of the films of elastomers formed, when the films were seven (7) days old, were then recorded. The numerical results are summarized in Table 2 below:
(b') Another portion of each of these two compositions was utilized to manufacture test-pieces in accordance with ASA Standard Specification 116-1-1960, each test-piece being manufactured in accordance with the process given under (b) of Example 1.
The test-piece were divided into three (3) batches of equal size and each batch was subjected to one of the tests also described under (b) of Example 1.
(i) First batch: the results relating to the measurement of the tensile strength (TS) and or the corresponding elongation (E/B) of the test-pieces are summarized in Table 3 below:
(ii) Second batch: the test-pieces were placed under tension by subjecting them to an elongation of 150%; these test-pieces were examined after aperiod of time of 24 hours and it was found that same passed the test; there were neither any cohesive or adhesive breaks.
(iii) Third batch: the test-pieces were immersed in water at 25.degree. C. for 96 hours and were then placed under tension as above.
These test-pieces were examined after a period of time of 24 hours and it was found that they too passed the test.
(c') A third portion of each of the compositions P.sub.2 and P.sub.3 was treated in accordance with the process described under (c) of Example 1, namely, by introducing the compositions into aluminum tubes, closing the tubes and heating for 48 hours at 100.degree. C.
After this accelerated ageing stage, the properties of the compositions were measured in accordance with the tests described above; it was found that the touch-dry time and hardening time were on the order of those included in Table (2), that the films of elastomer have essentially the same mechanical properties as those included in Table (2), and that the adhesion to ASA test-pieces had virtually the same values as those summarized in Table (3).
Example 3
90 parts of .alpha.,.omega.-dihydroxydimethylpolysiloxane oil having a viscosity of 100,000 mPa.s at 25.degree. C., 30 parts of a mixture of organic products having a viscosity of 90 mPa.s at 25.degree. C. and consisting of a distillation cut of branched dodecylbenzene having a boiling range of 302.degree.-385.degree. C. at atmospheric pressure, 2 parts of an .alpha.,.omega.-dihydroxymethylphenylpolysiloxane oil having a viscosity of 350 mPa.s at 25.degree. C., 12 parts of a pyrogenic silica having a specific surface area of 150 m.sup.2 /g, and 70 parts of calcium carbonate having a mean particle diameter of 5 microns were successively introduced into a malaxator.
The contents of the malaxator were triturated for 3 hours at a temperature of 100.degree. C. and under a pressure of 5,000 Pa. The paste (202 parts) thus formed was permitted to cool to about 60.degree. C. and the following were incorporated therein at this temperature: 5 parts of the silane of the formula C.sub.6 H.sub.5 Si(OCH.sub.3).sub.3, 4.5 parts of the silane of the formula H.sub.2 N(CH.sub.2).sub.3 Si(OCH.sub.3).sub.3 and 0.05 part of dibutyltin diacetate.
The entire mass was malaxated for 3 minutes at 60.degree. C.
The resulting composition was stored in a closed container impervious to moisture.
One portion of this composition was spread, as a 2 mm thick layer, on a polyethylene plate in accordance with the process described under (a) of Example 1. The behavior of the deposited layer, and also the characteristics of the rubbery film formed, when same was seven (7) days old, were then noted.
The results were as follows:
Touch-dry time =20 minutes
Hardening time =18 hours
Shore A hardness =25
Tensile strength in MPa =1.3
Elongation at break in % =500
Tear strength in N/cm =50
Elongation at tear in % =180
Another portion of this composition was heated at 100.degree. C. for 48 hours in accordance with the process described under (c) of Example 1. After cooling to 25.degree. C., the composition was spread, as a 2 mm thick layer, on a polyethylene plate and the behavior of the deposited layer, and also the mechanical properties of the film of elastomer formed, when same was seven (7) days old, were recorded.
The results were as follows:
Touch-dry time =25 minutes
Hardening time =20 hours
Shore A hardness =27
Tensile strength in MPa =1.1
Elongation at break in % =550
Tear strength in N/cm =45
Elongation at tear in % =150
Example 4
Three different compositions P.sub.4, P.sub.5 and P.sub.6 were prepared by adding, to the paste K.sub.1 (171 parts) prepared in Example 1, one of the crosslinking systems below:
Composition P.sub.4 : 6.4 parts of the silane of the formula Si(OCH.sub.3).sub.4, 3 parts of the amine of the formula: ##STR7## and 0.1 part of dibutyltin dilaurate.
The paste K.sub.1, the silane Si(OCH.sub.3).sub.4 and the amine were first heated in the malaxator for 2 hours at 100.degree. C. at atmospheric pressure, During this heating, about 1.3 parts of methanol were collected.
The dibutyltin dilaurate was then added to the contents of the malaxator, cooled to about 50.degree. C.
Composition P.sub.5 : 11 parts of the silane of the formula CH.sub.3 Si(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3, 3 parts of n-octylamine of the formula CH.sub.3 (CH.sub.2).sub.7 NH.sub.2 and 0.1 part of dibutyltin dilaurate.
In a first stage, the paste K.sub.1, the silane and the amine were heated in the malaxator for 6 hours at 110.degree. C. under a pressure of 5,000 Pa; about 5 parts of the alcohol CH.sub.3 OCH.sub.2 CH.sub.2 OH were evolved during this treatment. In a second step, the tin salt was introduced into the contents of the malaxator, cooled to about 50.degree. C.
Composition P.sub.6 : 6 parts of the silane of the formula CH.sub.3 Si(OCH.sub.3).sub.3, 4 parts of the diamine of the formula H.sub.2 NCH.sub.2 CH.sub.2 CH(CH.sub.3)CH.sub.2 C(CH.sub.3).sub.2 CH.sub.2 NH.sub.2 and 0.1 part of dibutyltin dilaurate.
In a first stage, the paste K.sub.1, the silane and the amine were heated in the malaxator for 6 hours at about 80.degree. C. at atmospheric pressure; about 2 parts of methanol were evolved during this treatment. In a second stage, the tin salt was introduced into the contents of the malaxator, cooled to about 45.degree. C.
One portion of each of these three (3) compositions was spread, under ambient conditions, as a 2 mm layer, on a polyethylene plate in accordance with the process described under (a) of Example 1. The behavior of the deposited layers, and also the characteristics of the films formed, when the films were seven (7) days old, were then recorded. The numerical results are summarized in Table 4 below:
Another portion of each of these 3 compositions was subjected to accelerated ageing by heating for 48 hours at 100.degree. C. in accordance with the process described under (c) of Example 1.
It was found that the behavior of these aged compositions was essentially identical to the behavior of the above compositions which had not been subjected to heat treatment.
Example 5
Three compositions P.sub.7, P.sub.8 and P.sub.9 were prepared by adding, to the paste K.sub.1 (171 parts) prepared in Example 1, one of the crosslinking systems below:
Composition P.sub.7 : 11 parts of the silane of the formula Si(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.4, 1 part of piperidine, 6 parts of the silane of the formula H.sub.2 N(CH.sub.2).sub.2 NH(CH.sub.2).sub.2 NH(CH.sub.2).sub.3 Si(OCH.sub.3).sub.3 and 0.1 part of dibutyltin dilaurate.
The mixture consisting of the paste K.sub.1 and of the above crosslinking system was malaxated for 10 minutes at 60.degree. C.
Composition P.sub.8 : 7 parts of the silane of the formula C.sub.6 H.sub.5 Si(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3, 2 parts of ethylenediamine, 4 parts ofthe sil of the formula H.sub.2 N(CH.sub.2).sub.3 O(CH.sub.2).sub.3 Si(OCH.sub.3).sub.3 and 0.1 parts of dibutyltin diacetate.
In a first stage, the paste K.sub.1, the two (2) silanes C.sub.6 H.sub.5 Si(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3 and H.sub.2 N(CH.sub.2).sub.3 O(CH.sub.2).sub.3 Si(OCH.sub.3 ).sub.3 and the ethylenediamine were heated in the malaxator at 60.degree. C. for 2 hours, and in a second stage, the tin salt was introduced into the contents of the malaxator, cooled to about 50.degree. C.
Composition P.sub.9 : 6 parts of the silane of the formula CH.sub.2 .dbd.CHSi(OCH.sub.3).sub.3, 1.5 parts of the amine of the formula CH.sub.3 (CH.sub.2).sub.3 NH.sub.2, 4 parts of the aminosilane of the formula H.sub.2 N(CH.sub.2).sub.2 S(CH.sub.2).sub.3 Si(OCH.sub.3).sub.3 and 0.1 part of dibutyltin diacetate.
The mixture consisting of the paste K.sub.1 and of the above crosslinking system was malaxated for 10 minutes at 60.degree. C.
One portion of each of these three (3) compositions P.sub.7, P.sub.8 and P.sub.9 was spread, under ambient conditions, as a 2 mm thick layer, in accordance with the process described under (a) of Example 1. The behavior of the deposited layers, and also the characteristics of the films formed, when the films were seven (7) days old, were then recorded. The numerical results are summarized in Table 5 below:
Another portion of each of these three (3) compositions was utilized to manufacture test-pieces in accordance with ASA Standard Specification 116-1-1960. The process for the manufacture of each test-piece was the one described under (b) of Example 1; however, the material constituting the plates of the test-pieces was based solely on aluminum.
The results relating to the measurement of the tensile strength (TS) and of the elongation at break (E/B) of the test-pieces are summarized in Table 6 below:
All these breaks were cohesive.
Another portion of each of these three (3) compositions was subjected to accelerated ageing by heating at 100.degree. C. for 48 hours in accordance with the process indicated under (c) of Example 1. The recorded behavior of these aged compositions was essentially identical to the behavior of the above compositions which had not been subjected to heat treatment.
Example 6
100 parts of an .alpha.,.omega.-dihydroxymethylphenylpolysiloxane oil having a viscosity of 30,000 mPa.s at 25.degree. C. and consisting of 94 mol % of (CH.sub.3).sub.2 SiO units and 6 mol % of (C.sub.6 H.sub.4).sub.2 SiO units, 15 parts of pyrogenic silica having a specific surface area of 300 m.sup.2 /g and treated with octamethylcyclotetrasiloxane, and 5 parts of an .alpha.,.omega.-dimethoxymethylphenylpolysiloxane oil having a viscosity of 50 mPa.s at 25.degree. C. and consisting of 70 mol % of (CH.sub.3).sub.2 SiO units and 30 mol % of (C.sub.6 H.sub.5).sub.2 SiO units were successively introduced into a malaxator.
The contents of the malaxator were mixed for 3 hours at a temperature of 110.degree. C and under a pressure of 5,000 Pa. The resulting paste (119 parts) was permitted to cool to about 60.degree. C and the following were incorporated therein: 7 parts of the silane of the formula CH.sub.2 .dbd.CH--CH.sub.W Si(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3, 4 parts of the silane of the formula H.sub.2 N(CH.sub.2).sub.3 O(CH.sub.2).sub.3 Si(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3 and 0.1 part of the dibutyltin dilaurate.
The entire mass was malaxated for 3 minutes at 60.degree. C. The resulting composition was divided into two (2) portions. One of the portions was spread, under ambient conditions, as a 2 mm thick layer, on a polyethylene plate in accordance with the process described under (a) of Example 1. The behavior of the deposited layer, and also the characteristics of the rubbery film formed, when same was seven (7) days old, were then noted. The results were as follows:
Touch-dry time =30 minutes
Hardening time =22 hours
Shore A hardness =20
Tensile strength in MPa =1.7
Elongation at break in % =350
The other portion was heated at 100.degree. C for 48 hours in accordance with the process described under (c) of Example 1. After cooling, this portion was also spread, also in the open atmosphere, as a 2 mm thick layer and the following numerical results were recorded:
Touch-dry time =40 minutes
Hardening time =25 hours
Shore A hardness =18
Tensile strength in MPa =1.3
Elongation at break in % =250
Example 7
100 parts of an .alpha., .omega.-dihydroxymethylvinylpolysiloxane oil having a viscosity of 4,000 mPa.s at 25.degree. C and consisting of 97 mol % of (CH.sub.3).sub.2 SiO units and 3 mol % of CH.sub.3 (CH.sub.2 =CH)SiO units, 20 parts specific surface area of 300 m.sup.2 /g and treated with octamethylcyclotetrasiloxane, and 20 parts of ground quartz having a mean particle diameter of 5 microns were successively introduced into a malaxator. The contents of the malaxator were mixed for 3 hours at 110.degree. C. and under a pressure of 4,500 Pa; the resulting paste (139.5 parts) was permitted to cool to about 50.degree. C. and the following were incorporated therein: 10 parts of the silane of the formula Si(OCH.sub.2 CH.sub.2 CH.sub.3).sub.4 , 5 parts of the silane of the formula H.sub.2 N(CH .sub.2 S(CH.sub.2).sub.3 Si(OCH.sub.3 ).sub.3 and .sub.0.1 part of dibutyltin diacetate. The entire mass was malaxated for 5 minutes at 50 .degree. C. The resulting composition was then divided into two (2) portions.
One of the portions was spread, under ambient conditions, as a 2 mm thick layer in accordance with the process described under (a) of Example 1. The behavior of the deposited layer and the characteristics of the film formed, when same was seven (7) days old, were then noted. The results were as follows:
Touch-dry time =8 minutes
Hardening time =10 hours
Shore A hardness =59
Tensile strength in MPa =2.7
Elongation at break in % =150
The other portion was heated for 48 hours at 100.degree. C. in accordance with the process described under (c) of Example 1; after cooling, this portion was also spread, under ambient conditions, as 2 mm thick layer and the following numerical results were recorded:
Touch-dry time =8 minutes
Hardening time =12 hours
Shore A hardness =62
Tensile strength in MPa =3.2
Elongation at break in % =120
While the invention has been described in terms of various preferred embodiments, the skilled artisan will appreciate that various modifications, substitutions, omissions, and changes may be made without departing from the spirit thereof. Accordingly, it is intended that the scope of the present invention be limited solely by the scope of the following claims.
Claims
What is claimed is:
1. A curable, pasty, one-component storage stable organopolysiloxane composition of matter consisting essentially of an intimate, water-free admixture of: (i) 100 parts by weight of .alpha..omega.-dihydroxydiorganopolysiloxane polymer having a viscosity of at least 500 mPa.s at 25.degree. C. and essentially consisting of diorganosiloxy units of he formula R.sub.2 SiO, in which the symbols R, which are identical or different, represent alkyl and haloalkyl radicals having from 1 to 8 carbon atoms, alkenyl radicals having from 2 to 4 carbon atoms, aryl and haloaryl radicals having from 6 to 8 carbon atoms or cyanoalkyl radicals having fro 3 to 4 carbon atoms, at least 50% of the total of such radicals being methyl radicals; (ii) 5 to 200 parts by weight of filler; (iii) 2 to 20 parts by weight of a polyalkoxylated organosilane having the structural formula: wherein R', is methyl, vinyl, allyl, methallyl or phenyl, and p and x are each zero or one; (iv) 0.5 to 115 parts by weight of an amine selected from the group consisting of primary and secondary organic amines having a PKb of less than 5 in an aqueous medium and having a boiling point of at least 60.degree. C. at at atmospheric pressure, and the aminoorganosilanes having the structural formula: in which the symbol R" represents a methyl or ethyl radical, the symbol G represents an alkylene radical having from 1 to 5 carbon atoms, the symbol X represents an oxygen or sulfur atom, the symbol G', represents an alkylene radical having from 2 to 5 carbon atoms, the symbol Y', represents a radical of the formula (G"NH).sub.k R"', in which the symbol G" represents an alkylene radical having from 2 to 6 carbon atoms, the symbol R"' represents a hydrogen atom or an alkyl radicla having from 1 to 4 carbon atoms and the symbol k represents zero, one, two or three, the symbol Y" represents a methyl vinyl or phenyl radical, the symbols p and y represent zero or one, with the proviso that, if p is one, R" can only be methyl, and the symbol m represents zero, on, two or three; and (v) 0.005 to 3 parts by weight of a curing catalyst selected from the group consisting of tin salts of carboxylic acids and organotin salts of carboxylic acids.
2. The composition of matter as defined by claim 1, wherein the component (i) R is selected from the group consisting of methyl, ethyl, propyl, isopropyl, butyl, pentyl, hexyl, 2-ethylhexyl, octyl, 3, 3, 3-trifluoropropyl, 4, 4, 4-trifluorobutyl, trifluorobutyl, 4, 4, 4, 3, 3-pentafluorobutyl, cyclopentyl, cyclohexyl, methylcyclohexyl, 2,3-difluorocyclobutyl, 3,4-difluoro-5-methylcycloheptyl, vinyl, allyl, but-2-enyl, phenyl, tolyl, xylyl, chlorophenyl, dichlorophenyl, trichlorophenyl, .beta.-cyanoethyl and Y-cyanopropyl.
3. The composition of matter as defined by claim 1, the filler component (ii) comprising particulates having a mean particle diameter of less than 0.1 micron and selected from the group consisting of pyrogenic silica, precipitation silica, pyrogenic titanium oxide, aluminum oxide and carbon black.
4. The composition of matter as defined by claim 1, the filler component (ii) comprising particulates having a mean particle diameter in excess of 0.1 micron and selected from the group consisting of ground quartz, diatomaceous silica, calcium carbonate, calcined clay, rutile titanium oxide, the oxides of iron, zinc, chromium, zirconium and magnesium, hydrated or non-hydrated alumina, boron nitride, lithopone, barium metaborate, powdered cork, wood sawdust, phthalocyanines, inorganic and organic fibers, and organic polymers.
5. the composition of matter as defined by claim 1, the polyalkoxylated organosilane (iii) being selected from the group consisting of Si(OCH.sub.3).sub.4, Si(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.4, CH.sub.3 Si(OCH.sub.3).sub.3, CH.sub.3 Si(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3, CH.sub.2 .dbd.CHSi(OCH.sub.3).sub.3, CH.sub.2 .dbd.CHSi(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3, CH.sub.2 .dbd.CH--CH.sub.2 Si(OCH.sub.3).sub.3, CH.sub.2 .dbd.CH--CH.sub.2 Si(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3, CH.sub.2 .dbd.C(CH.sub.3)CH.sub.2 Si(OCH.sub.3).sub.3, CH.sub.2 .dbd.C(CH.sub.3)CH.sub.2 Si(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3, C.sub.6 H.sub.5 Si(OCH.sub.3).sub.3 and C.sub.6 H.sub.5 Si(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3.
6. The composition of matter as defined by claim 5, said polyalkoxylated organosilane (iii) being selected from the group consisting of Si(OCH.sub.3).sub.4, Si(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.4, CH.sub.2 .dbd.CHSi(OCH.sub.3).sub.3, CH.sub.2 .dbd.CHSi(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3, C.sub.6 H.sub.5 Si(OCH.sub.3).sub.3 and C.sub.6 H.sub.5 Si(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3.
7. The composition of matter as defined by claim 1 the amine (iv) having the formula (Y).sub.s NH.sub.3-s, wherein s is one or two, and Y is alkyl having from 4 to 25 carbons when s is one, and alkyl having from 1 to 25 carbon atoms when s is two, with the proviso that the total number of carbon atom in the Y's, when s is two, ranges from 5 to 30.
8. The composition of matter as defined by claim 7, wherein the amine (iv) is selected from the group consisting of n-butylamine, amylamine, ##STR8## CH.sub.3 --CH.sub.2 --C(CH.sub.3).sub.2 NH.sub.2 n-decylamine, laurylamine, hexadecylamine, n-octylamine, di-(isopropyl)-amine, di(n-butyl)-amine and di-(isobutyl)-amine.
9. The composition of matter as defined by claim 1, the amine (iv) having the formula M(NHQ).sub.t NHM, in which the symbols M, which are identical or different, represent hydrogen atoms or alkyl radicals having from 1 to 10 carbon atoms, the symbol t represents one, two or three and the symbols Q, which are identical or different when t is two or three, represent alkylene radicals or --NH.sub.2 substituted alkylene radicals having from 1 to 25 carbon atoms.
10. The composition of matter as defined by claim 9, wherein the amine (iv) is selected from the group consisting of ethylenediamine, propylenediamine, hexamethylenediamine, ##STR9## H(NHCH.sub.2 CH.sub.2).sub.2 NH.sub.2, H(HNCH.sub.2 CH.sub.2).sub.3 NH.sub.2 and H.sub.2 NCH.sub.2 CH(NH.sub.2)CH.sub.2 NH.sub.2.
11. The composition of matter as defined by claim 1, wherein the amine (iv) is selected from the group consisting of cyclopentylamine, cyclohexylamine, ##STR10## piperidine, pyrrolidine, piperazine, ##STR11## benzylamine and phenylethylamine.
12. The composition of matter as defined by claim 1, wherein the amine (iv) is selected from the group H.sub.2 N(CH.sub.2).sub.3 Si(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3, H.sub.2 N(CH.sub.2).sub.3 Si(OCH.sub.3).sub.3, H.sub.2 N(CH.sub.2).sub.3 Si(OC.sub.2 H.sub.5).sub.3, H.sub.2 N(CH.sub.2).sub.4 Si(OCH.sub.3).sub.3, H.sub.2 NCH.sub.2 CH(CH.sub.3)CH.sub.2 CH.sub.2 SiCH.sub.3 (OCH.sub.3).sub.2, H.sub.2 NCH.sub.2 Si(CH.sub.3).sub.3, HN(n-C.sub.4 H.sub.9)CH.sub.2 Si(CH.sub.3).sub.3, H.sub.2 N(CH.sub.2).sub.2 NH(CH.sub.2).sub.3 Si(OCH.sub.3).sub.3, H.sub.2 N(CH.sub.2).sub.2 NH(CH.sub.2).sub.3 Si(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3, CH.sub.3 NH(CH.sub.2).sub.2 NH(CH.sub.2).sub.3 Si(OCH.sub.3).sub.3, H(NHCH.sub.2 CH.sub.2).sub.2 NH(CH.sub.2).sub.3 Si(OCH.sub.3).sub.3, H.sub.2 N(CH.sub.2).sub.2 NH(CH.sub.2).sub.3 Si(CH.sub.3).sub.3, ##STR12## H.sub.2 N(CH.sub.2).sub.3 O(CH.sub.2).sub.3 Si(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3, H.sub.2 N(CH.sub.2).sub.3 O(CH.sub.2).sub.3 Si(OCH.sub.3).sub.3, C.sub.2 H.sub.5 NH(CH.sub.2).sub.3 O(CH.sub.2).sub.3 Si(OCH.sub.3).sub.3, H.sub.2 N-CH.sub.2 -CH(CH.sub.3)CH.sub.2 O(CH.sub.2).sub.3 Sic.sub.6 h.sub.5 (OCH.sub.3).sub.2, H.sub.2 N-CH.sub.2 CH.sub.2 NH(CH.sub.2).sub.3 O(CH.sub.2).sub.3 Si(OCH.sub.3).sub.3, H.sub.2 N(CH.sub.2).sub.2 S(CH.sub.2).sub.3 Si(OCH.sub.2 CH.sub.2 OCH.sub.3).sub.3, H.sub.2 N(CH.sub.2).sub.2 S(CH.sub.2).sub.3 Si(OCH.sub.3).sub.3, and H(NHCH.sub.2 CH.sub.2).sub.2 S(CH.sub.2).sub.3 SiCH.sub.3 (OCH.sub.3).sub.2.
13. The composition of matter as defined by claim 1, further comprising up to 150 parts by weight per 100 parts of the polysiloxane (i) of an .alpha.,.omega.-bis-(triorganosiloxy)diorganopolysiloxane polymer having a viscosity of at least 10 mPa.s at 25.degree. C., the organic radicals bonded to the silicon atoms being selected from the group consisting of methyl, vinyl and phenyl radicals and at least 60% of such radicals being methyl radicals.
14. The composition of matter as defined by claim 13, wherein the .alpha..omega.-bis-(triorganosiloxy)-diorganosiloxane is at least partially replaced by polyalkylbenzenes obtained by alkylating benzene with long chain olefins which result from the polymerization of propylene.
15. A process for the preparation of the composition of matter as defined by claim 1, comprising the intimate mixing, in the absence of moisture, of components (i) through (v), followed by the removal of volatile components.
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