Molded article of metathesis polymerized polymer containing fillers and process for its preparation.

Field of the Invention

0001This invention relates to a molded article of a meta­thesis polymerized polymer containing fillers and a process for producing the same.

Background of the Invention

0002U.S. Patent 4,400,340 and U.S. Patent 4,426,502 disclose the production of a molded article by injecting two kinds of reactive solutions, one of which comprises a norbornene-type monomer such as dicyclopentadiene and a catalyst component of a metathesis polymerization catalyst system and the other comprises a norbornene type monomer and an activator component of the catalyst system under an impingement mixing into a mold in which the liquid mixture is metathesis polymerized in bulk (called "RIM process" hereinafter). The RIM process is a low pressure one-step or one-shot injection process and the liquid mixture injected into the mold polymerizes rapidly to form a molded article. Thus, there are easily and cheaply produced large-sized molded articles from norbornene-type monomers such as dicyclopentadiene by RIM process.

0003USP 4,598,102 discloses the addition of reinforcing agents or fillers such as glass, wollastonite, mica, carbon black, talc and calcium carbonate to the metathesis polymerizable com­position of cyclic olefin monomers.

0004Although such reinforcements are added to improve mechanical and physical properties, such as flexural modulus and strength, it has been observed that the addition of them does not necessarily achieve such improvement effectively. It is known that affinity between reinforcements and matrix polymers influen­ces mechanical and physical properties of the composites thereof and that good affinity generally improves those properties.

0005There are many prior art techniques to increase the affinity between the reinforcements and the matrix polymers. One of the techniques commonly used is to treat the reinforcements or the fillers with a coupling agent. Among coupling agents, there have been used most commonly silane coupling agents, having at least one group, which is hydrolyzable to silanol group and is bonded to silicon atom, and at least one group which imparts good affinity to the matrix polymers.

0006The silanol group may readily react with hydroxyl groups or other active groups existing on the surface of the reinforce­ments.

0007Thus, the silane couplers can act as a go-between of the matrix and the reinforcements.

0008As a matter of course, the groups which impart the good affinity to the matrix polymers should differ depending on the kinds of the polymers.

0009It has been found, for example, that vinylsilanes which were used previously as couplers for unsaturated polyesters (UPE), are not so effective. Therefore, methacryl silanes, are now used predominantly as couplers for UPE instead of vinylsilane.

0010Aminoalkyl silane couplers and epoxy-containing silane couplers are used for epoxy resins, polyurethanes, polyamides, polyimides, phenolic resins and the likes. Chloroalkylsilanes and mercapto-group-containing silane couplers are suitably used for such rubbers as EPDM, SBR, NR and polychloroprenes.

0011Silane couplers which impart good affinity to the above mentioned metathesis-polymerized polymers with fillers have been required to prepare composites having good properties.

0012So far as we are aware of, there was no prior informa­tion available on silane couplers imparting such good affinity to the metathesis polymerized polymers.

0013We have studied and tested the coupling effect of many silanes as to whether the silanes can increase the affinity of the metathesis polymerized polymers with the fillers and reinforcing materials or not. The tests of the coupling properties were carried out by measuring the bond strength between the metathesis polymerized polymers and a glass plate pretreated with one of the silanes.

0014As a result, we have found that, among many silanes, particular silanes having at least one hydrolyzable group bonded to silicon atom and at least one unsaturated group of the formula R¹-CH=CH-R²-, wherein R¹ is hydrogen or an alkyl group of 1-6 carbon atoms, and R² is a single bond or an alkylene group of 1-6 carbon atoms, which is bonded to silicon atom, have very excellent coupling properties and increase magnificently the affinity of the metathesis polymerized polymers with the fillers and reinforcing materials to reinforce largely the polymers. The selective and excellent coupling properties of these silanes for the metathesis polymerized polymers are beyond expectation, since these silanes have seldom been used recently to treat the reinforcements for usual polymers such as UPE, epoxy resins, polyurethane, phenol resins, polyamide and the like.

0015Further, it is an unexpected finding that said par­ticular silanes do not substantially damage the activity of the metathesis polymerization catalyst system, when used in the metathesis polymer systems.

0016Therefore, it is an object of the present invention to provide a molded article which is reinforced by fillers pretreated with said particular silanes.

0017A further object of the present invention is to provide a process for producing the reinforced molded articles containing the fillers.

Summary of the Invention

0018The present invention relates to a molded article produced by metathesis polymerizing in a mold a composition comprising at least one metathesis polymerizable monomer and a metathesis polymerization catalyst system in the presence of at least one filler, characterized in that the filler is treated with a silane coupler having at least one hydrolyzable group bonded to silicon atom and at least one group of the formula R¹-CH=CH-R²-, wherein R¹ is a hydrogen or an alkyl group of 1-6 carbon atoms; and R² is a single bond or an alkylene group of 1-6 carbon atoms, which is bonded to silicon atom.

0019The present invention further is in connection with a process for producing a molded article by introducing a metathesis polymerizable composition comprising at least one metathesis polymerizable monomer and a metathesis polymerization catalyst system into a mold in which the composition is metathesis polymer­ized to produce the molded article, characterized in that the composition is metathesis polymerized in the presence of at least one filler which is treated with a silane coupler having at least one hydrolyzable group bonded to silicon atom and at least one group of the formula R¹-CH=CH-R²-, wherein R¹ is a hydrogen or an alkyl group of 1-6 carbon atoms; and R² is a single bond or an alkylene group of 1-6 carbon atoms, which is bonded to silicon atom.

Detailed Description of the Invention

0020In the present invention, the silanes used to treat the fillers have at least one hydrolyzable group bonded to silicon atom and at least one group of the formula R¹-CH=CH-R²-, wherein R¹ and R² represent the same groups as mentioned above respectively, which is bonded to silicon atom.

0021The silanes are preferably of the formula R²-CH=CH-R²-Si(R³)_m(X)_3-m      (I) wherein R¹ and R² are the same as defined above, R³ is an alkyl group of 1-6 carbon atoms, X is a hydrolyzable group selected from the group consisting of halogen, alkoxy and acyloxy group option­ally having other polar group or groups, and m is 0, 1 or 2.

0022From the view point of affinity with the fillers, silanes of the formula R¹-CH=CH-R²-Si(X)₃      (II) wherein R¹, R² and X are the same groups as mentioned above, respectively, are more preferable.

0023The group R¹ in the silanes of the formulas (I) and (II) mentioned above is hydrogen, methyl, ethyl, straight or branched propyl, butyl, pentyl or hexyl. Among them, hydrogen or methyl, especially hydrogen, is preferable.

0024The group R² in silanes of the formulas (I) and (II) above is a single bond, methylene, straight or branched ethylene, propylene, butylene, pentylene or hexylene. Among them, the single bond or methylene is suitable.

0025R³ in silanes of the formula (I) is methyl, ethyl, straight or branched propyl, butyl, pentyl, hexyl, or methyl.

0026When m is 0 or 1 in the formula (I), silanes have two or three hydrolyzable group X, which may be the same or different. The group X can hydrolyze to hydroxyl group which reacts with polar groups on the surface of the fillers. The group X repre­sents alkoxy containing or not containing other polar group, such as methoxy, ethoxy, propoxy or methoxyethoxy; acyloxy such as acetoxy, propionyloxy or butyroyloxy; or halogen such as chloride, fluoride, bromide or iodide. The hydrolyzability of the group X increases in the order of chloride, acetoxy, methoxy and ethoxy in general.

0027Examples of preferable silanes used in the present invention include vinyltrimethoxysilane, vinyldimethoxychloro­silane, vinylmethoxydichlorosilane, vinyltrichlorosilane, vinyl­triethoxysilane, vinyldiethoxychlorosilane, vinylethoxydichloro­silane, allyltrimethoxysilane, allyldimethoxychlorosilane, allyl­trichlorosilane, allyltriethoxysilane allyldiethoxychlorosilane, allylethoxydichlorosilane, vinyltriacetoxysilane, vinyldiacetoxy­chlorosilane, vinylacetoxydichlorosilane, allyltriacetoxysilane, allyldiacetoxychlorosilane, allylacetoxydichlorosilane, vinyltris­(methoxyethoxy)silane, allyltris(methoxyethoxy)silane, vinyl­methyldimethoxysilane, allylmethyldimethoxysilane, vinylmethyl­diethoxysilane, allylmethyldiethoxysilane, vinylmethyldiacetoxy­silane, allylmethyldiacetoxysilane, vinylmethyldichlorosilane, allylmethyldichlorosilane, vinyldimethylmethoxysilane, allyl­dimethylmethoxysilane, vinyldimethylethoxysilane, allyldimethyl­ethoxysilane, vinyldimethylacetoxysilane, allyldimethylacetoxy­silane, vinyldimethylchlorosilane, allyldimethylchlorosilane, 2-­butenyltrimethoxysilane, 2-butenyltriethoxysilane, 2-butenyltri­acetoxysilane, 2-butenyltrichlorosilane and the like. Among them, vinyltriethoxysilane, vinyltris(methoxyethyl)silane, allyltri­ethoxysilane, allyltrimethoxysilane, 2-buthenyl-triethoxysilane, and 2-butenyl-trimethoxysilane are more preferable from a high coupling properties, easy workability, easy availability, low cost and the like.

0028It is desirable that the fillers have active groups such as hydroxyl group on their surface to react with the silanol group generated by hydration.

0029In the present invention, there may be used various inorganic or organic fillers, especially inorganic fillers, in the form of fiber, fabric, fiber mat, fiber preform, powder, particle, flake, micro-balloon and the like.

0030Examples of the inorganic fillers include synthetic and natural materials such as glass, alumina, silica, potassium titanates or other titanates aluminum silicate or other silicates, wollastonite, mica, kaolin, clay, talc, and the like. Also, some organic materials having active hydrogen, such as cellulose, polyamides phenol resins and the like, can be exemplified as the suitable fillers to be used for the above metathesis-polymerized systems by being treated with the above silanes.

0031Among many fillers, glass fillers are preferable. Any form of glass fillers may be used in the present invention. Examples of glass fillers include woven-, nonwoven- and knitt­ed-glass cloth made of glass filaments, glass fiber mat and glass fiber preform made by binding chopped glass strands or glass filaments with a binder or by needle punching the glass filaments, chopped glass fiber and strand, glass micro fiber, glass powder, glass particle, glass flake, glass microballoon and the like.

0032In the present invention, the fillers are treated with the particular silanes mentioned above. The treatment of the fillers with the silanes may be carried out according to any known process, for example, by applying a solution of the silane to the fillers, then drying and heating the fillers. As the solvent for the silane solution, there is used water, an organic polar solvent such as an alcohol, aceton, ether, ester, or a mixture thereof. In view of low cost and safety, water is preferable. In usual, about 0.5 - about 2 % of solutions of the silanes are preferably used for the treatment of the fillers.

0033During the drying and heating of the fillers treated with the silanes, the hydrolyzable group of the silanes hydrolyzes to hydroxyl group to react with active groups, such as hydroxyl, which exist on the surface of the fillers, and the silanes are bonded to the fillers. The drying and heating processes may be carried out suitably depending on the kinds of the silanes, fillers, solvent and the like. In case of glass fiber treated with an aqueous solution of vinyltriethoxy-silane, for example, the pretreated glass fiber is dried at a temperature of about 15 - about 30°C for about 6 - 24 hours and then heated at a temperature about 100 about 140°C for about 5 - 20 min.

0034In case of the fiber-based fillers or reinforcements, the silane couplers can conveniently be applied to the fibers as components of spinning finishing oil when the fibers are spun.

0035In the present invention, the treatment of the fillers with the silane is preferably carried out prior to the contact of the fillers with the metathesis polymerizable composition, since in-situ treatment of the fillers with the silanes in the meta­thesis polymerizable composition usually necessitates larger amount of the silanes to result in coupling effect of the silanes, leading to the decrease of the activity of the metathesis poly­merization catalyst system and the production of molded articles with undesirable surface characteristics, such as poor paint-­adhesion caused by silane residues.

0036The amount of the silanes to be applied to the fillers may be varied suitably depending on the kind of the fillers and the silanes, composition of the solvents used to treat the fillers and other factors.

0037For example, when the fillers are glass fiber, about 0.3 - about 3 g of the silane per 100 g of the fillers are applied to the fillers.

0038The pretreated fillers in the form of a small sized powder, flake, microfiber, particle or microballoon are usually added into the metathesis polymerizable composition before intro­ducing the composition into a mold. The metathesis polymerizable composition containing the fillers are introduced into the mold and metathesis polymerized there to produce a molded article. In this case, it is desirable to pay attention to the uniform disper­sion of the fillers in the composition and that a nozzle of an injection machine and an inlet of the mold are not blocked by the fillers.

0039When the fillers are fabric such as woven, non-woven or knitted cloth, fiber mat, fiber preform, large or long sized fiber, particle or flake, they are usually put in a mold before the metathesis polymerizable composition is introduced into the mold. In this case, it is desirable to remove air contained in the filler in order to fully impregnate the polymerizable composi­tion into the spaces between the fillers and in order to produce a molded article with no or less void. The removal of air from the filler may be carried out prior and/or simultaneous application of vaccum to the mold, into which metathesis polymerizable composi­tion is introduced.

0040The use of such filler as fabric, fiber mat, fiber preform, large or long sized fiber, flake and the like generally provides molded articles with more increased rigidity, dimensional stability, heat-distortion temperature and mechanical strengths such as flexural modulus, flexural strength, tensile strength, impact strength and the like than the use of small sized fillers such as powder, microfiber and the like, though the use of large or long sized fillers such as fabric makes the molding process somewhat complicated and requires a rather longer molding cycle time.

0041The amount of fillers can be suitably varied depending on the kind of the fillers, the size and shape of the molded articles, the properties required for the molded articles and the like. In general, the fillers are used in the amount of about 3-­50%, preferably about 5-40%, based on the volume of the molded articles. The strength of the molded articles generally increases as the amount of the fillers increases. The use of too much fillers, however, undesirably makes difficult the impregnation of the metathesis polymerizable composition into spaces of the mold and produces the molded articles having many voids or defects.

0042Usually it is preferable that the fillers are dispersed or placed uniformly in the molded articles. But, in some cases, the fillers may be dispersed or placed ununiformly in the molded articles according to the intended application. For example, the fillers may be placed only in a particular part of the molded articles required to be more strong. The fillers can be placed in one or both surfaces alone of the molded articles or in the intermediate part alone of the molded articles. The molded articles may comprise two or more kinds of the fillers.

0043For example, a woven glass cloth made of fine denier glass filaments or a paper may be placed in circumference of the molded article and a nonwoven glass fiber mat prepared from larger denier filaments may be placed in the middle of it to provide the molded article with both smooth surface and high strength. Further, the molded articles reinforced with glass fiber can contain foamed materials to decrease the weight.

0044In the present invention, the metathesis polymerizable monomers are preferably cycloalkenes having 1-3 metathesis polyme­rizable cycloalkene moieties, especially having at least one norbornene moiety. Examples of them include dicyclopentadiene (DCP), tricyclopentadiene, cyclopentadiene-methylcyclopentadiene-­codimer, 5-ethylidenenorbornene, 5-vinylnorbornene, 5-phenyl­ norbornene norbornene 5-cyclohexenylnorbornene, 1,4-methano-­1,4,4a,5,6,7,8,8a-octahydronaphthalene 1,4,5,8-dimethano-1,4,4a,­5,6,7,8,8a-octahydronaphthalene, 6-ethylidene-1,4,5,8-dimethano-­1,4,4a,5,7,8,8a-heptahydronaphthalene, 1,4,5,8-dimethano-1,4,4a­5,7,8,8a-hexahydronaphthalene, ethylene-bis(5-norbornene), tri­cyclo[8,2,1,0]trideca-5,11-diene, norbornadiene and the like.

0045They can be used alone or in the form of a mixture of some of them. Dicyclopentadiene or a mixture of dicyclopentadiene with at least one other monomer is preferable.

0046In the present invention, there may also be used other metathesis polymerizable cyclic compounds having at least one of hetero atoms such as oxygen, nitrogen and the like together with metathesis polymerizable cycloalkene moiety, preferably norbornene moiety.

0047The hetero atom forms a polar group in the structure of said cyclic compounds, and those cyclic compounds having the polar group can often moderate the metathesis polymerization reaction.

0048Preferred examples of the polar groups include ether groups, carboxylic ester groups, cyano group, N-substituted imido groups and the like.

0049Examples of cyclic compounds having the polar groups include [(5-norbornenyl)-methyl]phenyl ether, bis[(5-norbornenyl)-­methyl]ether, 5-methoxycarbonyl-norbornene, 5-methoxycarbonyl-5-­methylnorbornene, 5-[(2-ethylhexyloxy,-carbonyl]norbornene, ethylene-bis(5-norbornenecarboxylate), 5-cyanonorbornene, 6-cyano-­1,4,5,8-dimethano-1,4,4a,5,6,7,8,8a-octahydronaphthalene, N-­ butylnadic acid imide, 5-(4-pyridyl)norbornene and the like.

0050These cyclic compounds having polar groups are generally used with DCP and the like. It is also preferable that these other cyclic compounds have less impurities which inhibit the metathesis polymerization.

0051In general, as well known, the metathesis polymerization catalyst system is composed of two components, i.e., a main catalyst component and an activator component.

0052The metathesis polymerization reaction is an exothermal reaction and proceeds very rapidly. Under such situation, the polymerization often occurs before the mixture can be poured into a mold, and it makes the pouring of the mixture into the mold difficult and makes the production of large sized molded articles difficult.

0053Accordingly, in the present invention, the catalyst and the activator of the metathesis polymerization catalyst system are added to individual monomer solutions to form a multi-part reac­tive solution (i.e., a multi-part metathesis polymerizable com­position), and then the multi-part reactive solutions are mixed rapidly by means of impinging-mixing (the RIM process) or by using a static mixer or a dynamic rotary mixer, and finally the mixture is immediately poured into a mold wherein it is polymerized and molded.

0054In this method, the multi-part reactive solutions do not need to have the same composition of monomers in each part. The composition of the monomers of each solution may be changed freely taking final composition of the monomers into consideration.

0055As the catalyst component of the metathesis polymeriza­tion catalyst system are used compounds, especially halides, of tungsten, molybdenum, rhenium or tantalium, preferably, tungsten and molybdenum. Particularly preferable are tungsten compounds. Among tungsten compounds tungsten halides, tungsten oxyhalides and the like are preferred. Tungsten hexachloride and tungstenoxy­chloride are more preferred. Organo ammonium tungstate and molybdate may also be used. However, such tungsten halide com­pounds undesirably often initiate cationic polymerization im­mediately when added directly to the mixture of monomers. It is, therefore, preferable that they are previously suspended in an inert solvent such as, for example, benzene, toluene or chloroben­zene and solubilized by the addition of an alcoholic compound or a phenolic compound.

0056A chelating agent or a Lewis base is preferably added to the solution containing the tungsten compound in order to prevent such undesirable polymerization as cationic polymerization. Those additives may include acetylacetone, acetoacetic acid, alkyl esters of acetoacetic acid, tetrahydrofuran, benzonitrile and the like. About 1-5 moles of a chelating agent or a Lewis base is preferably used per mole of the tungsten compound. Under such situations, the reactive solution containing the monomers and the catalyst component of the metathesis polymerization catalyst system (sometimes called "Solution A" hereinafter) is kept stable sufficiently for practical use.

0057The activator components of the metathesis polymeriza­tion catalyst system include organic metal compounds such as alkylated products of metals of Group I - Group III in the Peri­odic Table, preferably, tetraalkyl tins, trialkyl tin hydrides, alkylaluminum compound and alkylaluminum halide compounds includ­ing diethylaluminum chloride, ethylaluminum dichloride, tri­octylaluminum, dioctylaluminum iodide, tetrabutyltin and the like. The activator component is dissolved in a mixture of monomers to form the other reactive solution (sometimes called "Solution B" hereinafter.

0058According to the present invention, in principle, the molded articles are produced by mixing said two reactive solutions (i.e. Solution A and Solution B) as already described above. The polymerization reaction, however, starts so rapidly when the above-mentioned composition is used, and so the undesirable initiation of polymerization often accompanied by partial gelling occurs before completion of filling of the mixed solution into the mold. In order to overcome the problem, it is preferable to use a polymerization moderating agent.

0059As such moderators are generally used Lewis bases, particularly, ethers, esters, nitriles and the like.

0060Examples of the moderators include ethylbenzoate, butyl ether, diglyme, diethyleneglycoldibutylether, benzonitrile and the like. Such moderators are generally added to the reactive solu­tion containing the activator component.

0061In this case, when a polar monomer which moderates the metathesis polymerization is used with DCP and the like in the reactive solution containing the activator component, the Lewis base may also be omitted.

0062When a tungsten compound is used as the catalyst com­ponent, the ratio of the tungsten compound to the above-mentioned monomers is about 1000:1 - about 15000:1, and preferably about 2000:1 on molar base. When an alkylaluminum compound is used as the activator component, the ratio of the aluminum compound to the above-mentioned monomers is about 100:1 - about 3000:1 and prefe­rably around a ratio of about 300:1 - about 1000:1 on molar base.

0063The amount of the masking agent or the moderator may be adjusted by experiments depending upon the amount of the catalyst system.

0064A variety of other additives may be used practically in the present invention together with the fillers to improve or to maintain characteristics of the molded articles. The additive include pigments, antioxidants, light stabilizers, macromolecular modifiers, flame retardants and the like. These additives must be added to the starting solutions, since they cannot be added after the solutions are polymerized to the solid molded polymer.

0065The additives may be added to either one or both of multipart reactive solutions. The additives must be ones being substantially unreactive with the highly reactive catalyst com­ponent and activator component of the metathesis polymerization catalyst system in the solutions to avoid troubles as well as inhibition of polymerization.

0066If a reaction between the additive and the catalyst system is unavoidable but does not proceed so rapidly, the addi­tives can be mixed with the monomers to prepare a third solution, and the third solution is mixed with the first and/or second solutions of the multi-part solutions immediately before pouring the mixture into a mold.

0067The molded articles of the invention may preferably contain an antioxidant. Phenol- and amine-anti-oxidants are suitable and they are added to the polymerizable solution pre­viously, usually to "Solution A". Examples of the antioxidants include 2,6-t-butyl-p-cresol, N,N′-diphenyl-p-phenylenediamine, tetrakis[methylene(3,5-di-t-butyl-4-hydroxycinnamate)]methane, methylene-4,4′-bis(3,5-di-t-butylphenol) and the like.

0068The molded articles of the invention may also contain other polymers, which are added to the monomer solution. Among said polymers, elastomers are more preferable, since they increase the impact strength of the molded articles and they effectively control the viscosity of the solution. Examples of the elastomers include styrenebutadiene rubber, polybutadiene, styrene-butadiene-­styrene triblock rubber, styrene-isoprene-styrene triblock rubber, polyisoprene, butyl rubber, ethylene-propylene rubber, ethylene-­propylene-diene terpolymer, nitril rubber and the like.

0069In the present invention, further, there may be added a compound which reduces the amount of the unreacted residual monomers in the molded articles to avoid the unpleasant odor originated from the unreacted monomers. Examples of such compound include α,α,α-trichlorotoluene, esters of trichloro acetic acid, phthalic chloride, benzoic anhydride, phosphorus oxychloride, benzensulfonic chloride and the like.

0070As described above, the molded articles of the invention are preferably prepared by simultaneous molding with polymerizing, i.e., by RIM process or pre-mix process including RTM and RI process. In RIM process, two parts of the monomer solutions of the metathesis polymerization composition are rapidly mixed in the impingement mixing head of a RIM machine and the mixture is poured into a mold wherein it polymerizes and is molded.

0071In pre-mix process, two-part monomer solutions contain­ing the catalyst component and the activator component respective­ly are previously mixed to prepare a pre-mixture and then the pre-­mixture is introduced into a mold. In the RIM and RTM process, when the fillers treated with the silanes are small or short sized ones such as milled glass and are added in the metathesis polymer­izable composition as mentioned above, the fillers are added in either of the reactive solutions or both of them.

0072In both the RIM process and pre-mix process, the mixture can be introduced into the mold under relatively low pressure so that an inexpensive mold is usable. The temperature inside the mold increases rapidly by heat of the polymerization reaction so that the polymerization reaction is completed in a short time. The molded article of the invention can be removed easily from the mold without a releasing agent, unlike the polyurethane-RIM process.

0073The surface of the molded articles has polarity probably by the oxidized layer formed on the surface so that conventional coatings such as epoxy, polyurethane and the like adhere to the surface well.

0074In the present invention, the fillers pretreated with the silanes having at lest one hydrolyzable group bonded to silicon atom and at least one group of the formula R¹-CH=CH-R²-, wherein R¹ and R² are the same groups as mentioned above respec­tively, which is bonded to silicon atom have very good affinity with the metathesis polymerizable composition and can improve the mechanical and physical properties of the molded articles prepared from the metathesis polymerizable composition more than the fillers treated with other commercially-available silanes than those used in the present invention.

0075Thus, the molded articles of the present invention have high impact strength, tensile strength, flexural strength, dimen­sion stability, flexural modulus, heat distortion temperature and the like.

0076The present invention provides a variety of molded articles which include large sized molded articles such as parts of various vehicles including transports and machines such as motor cars, automobiles, motorbikes, motorboats, snowmobiles, tractor, golf cart, etc. housing of electric and electronic instruments other article used for sports or leisure sports and the like.

0077This invention described herein is illustrated by the following examples. These examples do not limit the invention.

Example 1:

(1) {Preparation of ingredients}

0078Commercially available dicylopentadiene DCP was purified by distillation under nitrogen reduced pressure to produce purified DCP with a freezing point of 33.4°C. The purity was determined by gas chromatography to be not less than 99%.

0079There was used commercially available highly pure ethylidene norbornene (ENB) having a purity of above 99% deter­mined by gas chromatography.

[Preparation of a concentrated catalyst component solution]

008019.80 g (0.05 Mole) of tungsten hexachloride was added to 90 ml of anhydrous toluene under nitrogen and then a solution consisting of 0.925 g of t-butanol and 5 ml of toluene was added. After the mixture was stirred for one hour, a solution consisting of 11.05 g (0.05 mole) of nonylphenol and 5 ml of toluene was added and then stirred for one hour under nitrogen. 10 g Of acetylacetone was added and then the solution was purged with nitrogen overnight to remove hydrogen chloride gas formed by the reaction of tungsten hexachloride with nonylphenol. Toluene was added to the resulting solution to prepare a concentrated-cataly­st-component-solution containing 0.5 M tungsten in terms of the metal content.

[Preparation of a concentrated activator component solution]

008131.17 g Of tri-n-octylaluminum, 5.70 g of di-n-octyl­ aluminum iodide and 13.42 g of diglyme were mixed under nitrogen, and then DCP was added to prepare a concentrated-activator-com­ponent-solution containing 1.0 M aluminum in terms of the metal-­content.

[Preparation of a solution containing mixed monomers]

0082DCP and ENB were mixed in the weight ratio of 96.5:3.5 to prepare a mixed-monomers-solution.

[Preparation of solution containing the catalyst component in a standard concentration]

00831000 g Of the mixed-monomers-solution was introduced into a glass bottle provided with a salem cap. After the suffi­cient purge with nitrogen, 16.2 ml of the concentrated catalyst component solution was introduced into the bottle using a syringe, and then the mixture was stirred enough to prepare a solution containing 0.001 M tungsten in the term of the metal content (Solution A).

[Preparation of a solution containing the activator component in a standard concentration]

00841000 g Of the mixed-monomers-solution was introduced into a glass bottle provided with a salem cap. After the suffi­cient purge with nitrogen, 23.7 ml of the concentrated activator component solution was introduced into the bottle by a syringe, and then the mixture was stirred enough to prepare a solution containing 0.003 M aluminum in terms of metal content (Solution B).

[Preparation of aqueous solution or dispersion containing silane]

0085Each of silanes recited in table 1 below was dissolved or dispersed in water to prepare each of aqueous solutions or dispersions containing 1 weight % of silane. pH Of the aqueous solutions or dispersions was adjusted as shown in Table 1. <tables id="tabl0001" num="0001"><table frame="all"><title>Table 1</title><tgroup cols="3" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="52.50mm" /><colspec colnum="2" colname="col2" colwidth="52.50mm" /><colspec colnum="3" colname="col3" colwidth="52.50mm" /><thead valign="top"><row><entry namest="col1" nameend="col1" align="left"><u style="single">Aqueous Solution or Dispersion of Silane</u></entry><entry namest="col2" nameend="col2" align="center"><u style="single">Kinds of Silane</u></entry><entry namest="col3" nameend="col3" align="center"><u style="single">pH of Aqueous Solution or Dispersion</u></entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">a</entry><entry namest="col2" nameend="col2" align="left">vinyltriethoxysilane</entry><entry namest="col3" nameend="col3" align="char" char=".">3.5</entry></row><row><entry namest="col1" nameend="col1" align="left">b</entry><entry namest="col2" nameend="col2" align="left">allyltriethoxysilane</entry><entry namest="col3" nameend="col3" align="char" char=".">3.5</entry></row><row><entry namest="col1" nameend="col1" align="left">c</entry><entry namest="col2" nameend="col2" align="left">(γ-methacryloxy)propyltrimethoxysilane</entry><entry namest="col3" nameend="col3" align="char" char=".">4.0</entry></row><row><entry namest="col1" nameend="col1" align="left">d</entry><entry namest="col2" nameend="col2" align="left">N-β-(N-vinylbenzylaminoethyl)-γ-aminopropyltrimethoxysilanehydrochlorate</entry><entry namest="col3" nameend="col3" align="char" char=".">7.0</entry></row><row><entry namest="col1" nameend="col1" align="left">e</entry><entry namest="col2" nameend="col2" align="left">γ-aminopropyltriethoxysilane</entry><entry namest="col3" nameend="col3" align="char" char=".">7.0</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">f</entry><entry namest="col2" nameend="col2" align="left">γ-chloropropyltriethoxysilane</entry><entry namest="col3" nameend="col3" align="char" char=".">4.5</entry></row></tbody></tgroup></table></tables>

(2) {Tests for coupling effect of silanes and test for influence of silanes on metathesis polymerization}

[Treatment of inner surface of glass containers]

0086Each of the aqueous relations and dispersions (a)-(f) prepared as above was applied on an inner surface of glass con­tainers having an diameter of 5.5 cm and a depth of 10 cm in the amount of 0.1 g of the aqueous solutions or dispersion (a)-(f) per 700 cm² of the inner surface. The inner surface of the glass containers was dried at the temperature of 20°C for 24 hours and then heated at the temperature of 120°C for 10 minutes.

[Introduction of Solution A and Solution B into glass container]

0087Solution A and Solution B prepared as above were intro­duced into each of two syringes respectively and maintained at 30°C.

0088From each of the two syringes, 10 ml of Solution A and 10 ml of Solution B were introduced into the glass container coated with each of the aqueous solutions and dispersions (a)-(f) as above and stirred enough to be mixed. After stirring, a thermocouple was inserted into the glass container and the time when the temperature of the mixture reached 100°C after the introduction into the glass container was measured as "polymeri­zation time". Results are shown in Table 2 below.

0089Further, the coupling effect of the silanes was tested by examining whether the polymers prepared in the glass containers are peeled off from the inner surface of the glass containers or not. The tests of the coupling effect of the silanes were carried out by hand-peeling off. The results are shown in Table 2.

0090As a comparison, the same procedures and tests as above were repeated except that the inner surface of the glass container was not treated with the aqueous solution and dispersions (a)-(f). The results are also shown in Table 2. <tables id="tabl0002" num="0002"><table frame="all"><title>Table 2</title><tgroup cols="4" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="39.37mm" /><colspec colnum="2" colname="col2" colwidth="39.37mm" /><colspec colnum="3" colname="col3" colwidth="39.37mm" /><colspec colnum="4" colname="col4" colwidth="39.37mm" /><thead valign="top"><row><entry namest="col1" nameend="col1" align="left"><u style="single">Aqueous Solution or Dispersion of Silane</u></entry><entry namest="col2" nameend="col2" align="center"><u style="single">Kinds of Silane</u></entry><entry namest="col3" nameend="col3" align="center"><u style="single">Polymerization Time (sec.)</u></entry><entry namest="col4" nameend="col4" align="center"><u style="single">Coupling-effect test of Silane</u></entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">a</entry><entry namest="col2" nameend="col2" align="left">vinyltriethoxysilane</entry><entry namest="col3" nameend="col3" align="right">48</entry><entry namest="col4" nameend="col4" align="left">not peeled off</entry></row><row><entry namest="col1" nameend="col1" align="left">b</entry><entry namest="col2" nameend="col2" align="left">allyltriethoxysilane</entry><entry namest="col3" nameend="col3" align="right">42</entry><entry namest="col4" nameend="col4" align="left">not peeled off</entry></row><row><entry namest="col1" nameend="col1" align="left">c</entry><entry namest="col2" nameend="col2" align="left">(γ-methacryloxy)propyltrimethoxysilane</entry><entry namest="col3" nameend="col3" align="right">55</entry><entry namest="col4" nameend="col4" align="left">peeled off</entry></row><row><entry namest="col1" nameend="col1" align="left">d</entry><entry namest="col2" nameend="col2" align="left">N-β-(N-vinylbenzylaminoethyl)-γ-aminopropyltrimethoxysilanehydrochlorate</entry><entry namest="col3" nameend="col3" align="right">62</entry><entry namest="col4" nameend="col4" align="left">peeled off</entry></row><row><entry namest="col1" nameend="col1" align="left">e</entry><entry namest="col2" nameend="col2" align="left">γ-aminopropyltriethoxysilane</entry><entry namest="col3" nameend="col3" align="right">71</entry><entry namest="col4" nameend="col4" align="left">peeled off</entry></row><row><entry namest="col1" nameend="col1" align="left">f</entry><entry namest="col2" nameend="col2" align="left">γ-chloropropyltriethoxysilane</entry><entry namest="col3" nameend="col3" align="right">53</entry><entry namest="col4" nameend="col4" align="left">peeled off</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">not used</entry><entry namest="col2" nameend="col2" align="left">--</entry><entry namest="col3" nameend="col3" align="right">35</entry><entry namest="col4" nameend="col4" align="left">peeled off</entry></row></tbody></tgroup></table></tables>

0091Though, the aqueous solutions or dispersions containing each of the silanes were not applied on fillers but applied on the inner surface of the glass containers, the results of Table 2 show that vinyltriethoxysilane and allyltriethoxy-silane increase the affinity of the metathesis polymerized copolymer of DCP and ENB with glass and bind strongly the copolymer with glass, while other silanes do not increase the affinity of the copolymer with glass.

0092The results of Table 2 also show that vinyltriethoxy­silane and allyltriethoxysilane less decrease the activity of the metathesis polymerization catalyst system than other silanes.

Example 2: {Tests for coupling effect of silanes}

0093Each of the aqueous solutions and dispersions (a)-(f) in Table 1 was applied on a glass plate of 2 mm thick in an amount of 0.5 g of each of the aqueous solutions and dispersions (a)-(f) per 100 cm² of the glass plate. The glass plate was dried at 20°C for 24 hours and then was heated at 120°C for 10 minutes.

0094The glass plate coated with each silane was placed inside of a mold of a micro-RIM machine in such a manner that the silane-coated surface of the glass plate faced a metathesis polymerizable composition to be injected into the mold.

0095Solution A and Solution B prepared in Example 1 were introduced into two syringes respectively. 10 ml Of Solution A and 10 ml of Solution B were injected from the two syringes into the mold under impingement-mixing to produce each of plaques of DCP/ENB copolymer.

0096There were obtained plaques to which surface the glass plate was bonded strongly when the glass plate coated with the aqueous solution (a) or (b) shown in Table 1 was put in the mold, though the glass plate was somewhat broken with the shrink of the plaques of DCP/ENB copolymer.

0097On the other hand, the glass plate was not bonded to the surface of the plaque when the glass plate put in the mold was coated with each of the aqueous solutions and dispersions (c)-(f) or was not coated with the aqueous solutions and dispersions (a)-­(f).

0098These results also show that silanes having vinyl or allyl group bonded to silicon atom with hydrolyzable group can increase the affinity of glass with the molded articles of the metathesis polymerized polymer.

Example 3: {Production of composite containing woven glass cloth}

0099Each of woven glass cloths (plain weave; 215 g/cm²; 0.22 mm thick) was heated at the temperature of 350°C for 60 hours to remove any coating or sizing on its surface. Then the woven glass cloth was dipped in each of the aqueous solutions and dispersions (a)-(f) in Table 1 and then taken out from the aqueous solution or dispersion. The excess aqueous solution or dispersion on each glass cloth was removed from the cloth by passing through between two squeezing rollers. Each cloth was dried at room temperature for 1 day and then heated at the temperature of 120 C for 10 minutes. Ten sheets of the woven glass cloth prepared as above were piled up in a mold.

0100Solution A having the same composition as that prepared in Example 1, which further contained 2%, based on the weight of the monomers (i.e. DCP and ENB), styrene-butadiene rubber avail­able from Firestone Co. as SBR-Stereon 720 and Solution B having the same composition as that prepared in Example 1, which further contained 2%, based on the weight of the monomers of the same rubber as above were poured into two service tanks of a RIM ma­chine, respectively.

0101Solution A and Solution B in the tanks were injected through the inpingement-mixing head of the RIM machine into the mold to produce each of DCP/ENB copolymer plate composites com­prising piled-up woven glass cloths.

0102As a comparison, the same procedures as above was repeated except that the woven glass cloths not treated with the aqueous solutions and dispersions (a)-(f) in Table 1 were piled up in a mold.

0103The flexural strength and flexural modulus of each of the composite plates produced above were measured.

0104The results are shown in Table 3 below. <tables id="tabl0003" num="0003"><table frame="all"><title>Table 3</title><tgroup cols="3" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="52.50mm" /><colspec colnum="2" colname="col2" colwidth="52.50mm" /><colspec colnum="3" colname="col3" colwidth="52.50mm" /><thead valign="top"><row><entry namest="col1" nameend="col1" align="center"><u style="single">Kind of aqueous Solution or Dispersion of Silane</u></entry><entry namest="col2" nameend="col2" align="center"><u style="single">Flexural Strength of Plate Composite (kg/cm²)</u></entry><entry namest="col3" nameend="col3" align="center"><u style="single">Flexural Modulus of Plate Composite (kg/cm²)</u></entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">a</entry><entry namest="col2" nameend="col2" align="right">1700</entry><entry namest="col3" nameend="col3" align="right">83000</entry></row><row><entry namest="col1" nameend="col1" align="left">b</entry><entry namest="col2" nameend="col2" align="right">1800</entry><entry namest="col3" nameend="col3" align="right">85000</entry></row><row><entry namest="col1" nameend="col1" align="left">c</entry><entry namest="col2" nameend="col2" align="right">1290</entry><entry namest="col3" nameend="col3" align="right">61500</entry></row><row><entry namest="col1" nameend="col1" align="left">d</entry><entry namest="col2" nameend="col2" align="right">910</entry><entry namest="col3" nameend="col3" align="right">43500</entry></row><row><entry namest="col1" nameend="col1" align="left">e</entry><entry namest="col2" nameend="col2" align="right">1320</entry><entry namest="col3" nameend="col3" align="right">57500</entry></row><row><entry namest="col1" nameend="col1" align="left">f</entry><entry namest="col2" nameend="col2" align="right">1230</entry><entry namest="col3" nameend="col3" align="right">60500</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">not used</entry><entry namest="col2" nameend="col2" align="right">1370</entry><entry namest="col3" nameend="col3" align="right">68500</entry></row></tbody></tgroup></table></tables>

0105The results of Table 3 show that the plate composites of the present invention, in which the glass cloth reinforcements were treated with silane couplers having vinyl or allyl group bonded to silicon atom, have increased flexural strength and flexural modulus compared to the plate composite in which the glass cloth reinforcements were not treated with silane coupler, while the plate composites, in which the glass cloths were treated with other commonly used silane couplers as shown in Table 1, show rather less flexural strength and flexural modulus than the plate composite in which the glass cloths were not treated with any silane couplers.