WO2004005393A1 - Duroplastiques liquides - Google Patents

Duroplastiques liquides Download PDF

Info

Publication number
WO2004005393A1
WO2004005393A1 PCT/EP2002/007276 EP0207276W WO2004005393A1 WO 2004005393 A1 WO2004005393 A1 WO 2004005393A1 EP 0207276 W EP0207276 W EP 0207276W WO 2004005393 A1 WO2004005393 A1 WO 2004005393A1
Authority
WO
WIPO (PCT)
Prior art keywords
resins
acid
resin
silica
duroplastics
Prior art date
Application number
PCT/EP2002/007276
Other languages
English (en)
Inventor
Werner Michel
Rüdiger Nowak
Pia Hofacker
Jürgen Meyer
Original Assignee
Degussa Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Degussa Ag filed Critical Degussa Ag
Priority to CN02829252A priority Critical patent/CN100575403C/zh
Priority to PCT/EP2002/007276 priority patent/WO2004005393A1/fr
Priority to AU2002321158A priority patent/AU2002321158A1/en
Priority to JP2004518475A priority patent/JP2005531672A/ja
Priority to EP02754810A priority patent/EP1517949A1/fr
Priority to TW092117450A priority patent/TW200401798A/zh
Publication of WO2004005393A1 publication Critical patent/WO2004005393A1/fr

Links

Classifications

    • 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
    • C08K9/04—Ingredients treated with organic substances
    • C08K9/06—Ingredients treated with organic substances with silicon-containing compounds

Definitions

  • the invention relates to a method of reinforcing liquid duroplastics, and to the resulting duroplastics.
  • Duroplastics refers to all plastics produced from curable resins. According to DIN 7724, up to the decomposition temperature they are crosslinked, close-meshed, highly polymeric materials, which are steel-elastic at lower temperatures and behave elastically with very limited deformability between 50°C or a higher temperature and the decomposition temperature. The shear modulus does not fall below 10 2 kp/cm 2 at any temperature.
  • Duroplastics are generally amorphous. As a result of the crosslinking of the duroplastics, their molecules are unable to conduct any macro-Brownian movements. Micro-
  • duroplastics is identical with the designation duromer, which is sometimes preferred because it is more closely connected in terms of form with elastomers and plastomers (thermoplastics) as designations for the two other classes of plastics.
  • Duroplastics are widely used as moulding compositions, cast resins, resin adhesives and lacquer resins.
  • the duroplastics include inter alia the commercially important groups of materials (abbreviations according to DIN 7728, PI, 1st January 1988, in brackets) of the diallyl phthalate resins (DAP) , epoxy-melamine-formaldehyde resins (MF) , melamine-phenol-formaldehyde resins (MP) , phenol-formaldehyde resins (PF) and unsaturated polyester resins (UP) . It is known to use pulverulent silica as a filler for polymers.
  • the filler finely distributed in the form of a hard phase surrounded by the softer polymer, improves a number of commercially valuable mechanical properties. These include hardness, tensile strength, stress values and other measurable properties.
  • thermoplastic polymers In principle, a distinction must be made between thermoplastic polymers and crosslinkable polymers. Silica can be used as a filler in both classes of materials. However, the added amounts and the effects can be very different owing to the polymer.
  • silica as a thickener in liquid duroplastics. That is not the subject of this invention, however; rather, the thickening action of the silica should be as little as possible.
  • the present invention describes the use of a silica modified with unsaturated organic groups in low molecular weight, generally liquid, reactive polymers. It is shown that it is possible to achieve an advantageous combination of rheological properties and mechanical properties, namely low viscosity and low flow limit in the uncrosslinked state on the one hand, and high hardness and high modulus in the crosslinked state on the other hand.
  • silanes themselves and the cleavage products formed therefrom are a source of risk in respect of combustibility and toxicity and often require additional safety measures and investment. It is therefore desirable to use a filler which already contains the desired reactive groups and does not release any undesirable substances into the polymer or into the environment.
  • the invention provides a method of reinforcing liquid duroplastics, which method is characterised in that a mixture of the uncrosslinked resin and a pyrogenically prepared silica which has been surface-modified with silanes containing methacrylic groups is prepared.
  • the invention also provides liquid duroplastics which are characterised in that they contain pyrogenically prepared silica which has been surface-modified with silanes containing methacrylic groups.
  • the pyrogenically prepared silica may be structurally modified.
  • a particularly effective filler is a silica which contains methacrylic groups and has been prepared by flame hydrolysis and whose structure has been altered by mechanical after-treatment.
  • BET surface area m 2 /g from 20 to 380 particle size nm from 6 to 110 tamped density g/1 from 50 to 600 pH value from 3 to 10 carbon content % from 0.1 to 15
  • DBP number % ⁇ 200 It can be prepared by intensively mixing a silica in a suitable mixing device first with water or dilute acid and then with the surface-modifying agent, or by applying a mixture of various surface-modifying agents by spraying. The components are mixed further for a period of from 15 to 30 minutes and then subjected to heat treatment at a temperature of from 100 to 400°C over a period of from 1 to 6 hours.
  • a pyrogenically prepared silica can be used as the silica.
  • Pyrogenic silicas are prepared by flame hydrolysis of volatile silicon compounds, such as, for example, SiCl 4 , methyltrichlorosilane or the like. They are known from ⁇ llmann's Enzyklopadie der ischen Chemie 4th edition, Volume 21, page 464 (1982) .
  • a pyrogenic silica having a BET surface area of approximately 200 m 2 /g can be used.
  • surface-modifying agents there may be used monomeric substances, such as methacryloxypropyltrialkoxysilanes, in which alkoxy can mean methoxy, ethoxy and/or propoxy.
  • An essential feature of the mentioned invention is the linking of the filler with the reactive monomers and oligomers of the lacquer by photopolymerisation.
  • aromatic amines metal salts of organic acids, e.g. cobalt compounds,
  • unsaturated polyesters there are suitable the conventional polycondensation products of polyvalent, especially divalent, carboxylic acids and their esterifiable derivatives, especially anhydrides, which are linked in the manner of esters to polyhydric, especially dihydric, alcohols, and optionally additionally contain radicals of monohydric alcohols and/or radicals of hydroxycarboxylic acids, wherein at least some of the radicals must have ethylenically unsaturated copolymerisable groups.
  • polyhydric, especially dihydric, optionally unsaturated alcohols there are suitable the conventional alkanediols and oxaalkanediols having acyclic or cyclic groups, such as, for example, ethylene glycol, 1, 2-propylene glycol, 1,3- propanediol, 1,3-butylene glycol, 1, 4-butanediol, 1,6- hexanediol, 2, 2-dimethylene-l, 3-propanediol, diethylene glycol, triethylene glycol, polyethylene glycol, dipropylene glycol, 1, 2-cyclohexanediol, 2,2- bis- (hydroxy-cyclohexyl) -propane, trimethylolpropane monoallyl ether or 1, 4-butanediol .
  • ethylene glycol 1, 2-propylene glycol, 1,3- propanediol, 1,3-butylene glycol, 1, 4-butanediol, 1,6-
  • ethylenehexanol fatty alcohols
  • benzyl alcohols 1, 2-di- (allyloxy) -propanol- (3)
  • glycerol pentaerythritol or trimethylolpropane.
  • the polyhydric, especially dihydric, alcohols are generally reacted in a stoichiometric amount with polybasic, especially dibasic, carboxylic acids or their condensable derivatives.
  • Suitable carboxylic acids and their derivatives are dibasic, olefinically unsaturated, preferably ⁇ - olefinically unsaturated, carboxylic acids, such as, for example, maleic acid, fumaric acid, chloromaleic acid, itaconic acid, methyleneglutaric acid and mesaconic acid and their esters or, preferably, their anhydrides.
  • polyesters such as, for example, succinic acid, glutaric acid, methylglutaric acid, adipic acid, sebacic acid, pimelic acid, phthalic anhydride, o-phthalic acid, isophthalic acid, terephthalic acid, dihydrophthalic acid, tetrahydro- phthalic acid, tetrachlorophthalic acid, 3,6- endomethylene.1, 2, 3, 6-tetrahydrophthalic acid, endomethylenetetrachlorophthalic acid or hexachloro- endomethylenetetrahydrophthalic acid, also mono-, tri- and higher-basic carboxylic acids, such as, for example, ethylhexanoic acid, fatty acids, methacrylic acid, acrylic acid, propionic 1, 2, 4, 5-benzene- te
  • Such readily crystallising unsaturated polyesters may be composed, for example, of fumaric acid, adipic acid, terephthalic acid, ethylene glycol, 1, 4-butanediol, 1, 6-hexanediol and neopentyl glycol.
  • the unsaturated polyesters have acid numbers of from 5 to 200, preferably from 20 to 85, and mean molecular weights of approximately from 800 to 6000, preferably from approximately 1000 to 4000.
  • the amorphous and optionally crystallisable unsaturated polyesters are generally prepared from their starting components by melt condensation under azeotropic conditions according to continuous or discontinuous processes.
  • Suitable copolymerisable, ethylenically unsaturated monomeric compounds are the allyl and, preferably, vinyl compounds conventionally used in the preparation of unsaturated polyester moulding compositions, for example vinyl aromatic compounds, such as styrene, methylenestyrene, p-chlorostyrene or vinyltoluene; esters of acrylic acid and methacrylic acid with alcohols having from 1 to 18 carbon atoms, such as methacrylic acid methyl ester, acrylic acid butyl ester, ethylhexyl acrylate, hydroxypropyl .
  • vinyl aromatic compounds such as styrene, methylenestyrene, p-chlorostyrene or vinyltoluene
  • esters of acrylic acid and methacrylic acid with alcohols having from 1 to 18 carbon atoms such as methacrylic acid methyl ester, acrylic acid butyl ester, ethylhexyl acrylate, hydroxypropy
  • acrylate dihydrodicyclopentadienyl acrylate, butanediol diacrylate and (meth) acrylic acid amides
  • allyl esters such as diallyl phthalate
  • vinyl esters such as ethylhexanoic acid vinyl ester, vinyl acetate, vinyl propionate, vinyl pivalate and others.
  • olefinically unsaturated monomers Preferably suitable as component B are styrene, vinyltoluene and diallyl phthalate.
  • the monomers B are contained in the polyester moulding compositions generally in an amount of from 10 to 80 wt.%, preferably from 20 to 70 wt.%, based on the total weight of components A and B.
  • reinforcing fibres there are suitable inorganic or organic fibres in the form of rovings or flat structures optionally woven therefrom, such as mats, for example of glass, carbon fibres, asbestos, cellulose and synthetic organic fibres, such as polycarboxylic acid esters, polycarbonates and polyamides.
  • the reinforcing fibres are used in amounts of from 5 to 300 wt.%, preferably from 10 to 150 wt.%, based on components A+B.
  • Suitable fillers are, for example, conventional finely powdered or granular inorganic fillers, such as chalk, kaolin, quartz powder, dolomite, heavy spar, metal powder, aluminium hydrate, cement, talcum, kieselguhr, wood dust, wood shavings, pigments and the like. They are used in SMC moulding compositions in amounts of from 0 to 200 wt.%, in BMC moulding compositions in amounts of from 100 to 400 wt.%, based on A+B.
  • SMC moulding compositions in amounts of from 0 to 200 wt.%
  • BMC moulding compositions in amounts of from 100 to 400 wt.%, based on A+B.
  • thickeners there may be mentioned, for example, alkaline earth oxides or hydroxides, such as calcium oxide, calcium hydroxid, magnesium hydroxide and, preferably, magnesium oxide, as well as mixtures of their oxides or hydroxides. They may also be partially replaced by zinc oxide. Polyisocyanates or metal alcoholates are also suitable in some cases.
  • the thickeners are added to the moulding compositions in amounts of from 0.5 to 5 wt.%, based on A+B.
  • polymerisation initiators there are used conventional organic peroxides that generate free radicals at elevated temperature, in amounts of from 0.05 to 5 wt.%, preferably from 0.1 to 3 wt.%, based on the total weight of components A and B.
  • Suitable initiators are, for example: benzoyl peroxide, tert- butyl peroctoate, tert-butyl perbenzoate, dicumyl peroxide, di-tert-dibutyl peroxide and perketals, such as, for example, trimethylcyclohexamonperketal, as well as percarbonates .
  • inhibitors such as hydroquinone, 2,6- dimethylhydroquinone, tert-butylbenzocatechin, p- benzoquinone, chloranil, 2, 6-dimethylquinone, nitrobenzenes, such as m-dinitrobenzene, thiodiphenylamine or salts of N-nitroso-N- cyclohexylhydroxylamine, as well as mixtures thereof.
  • the inhibitors are contained in the moulding compositions generally in an amount of from 0.005 to 0.2 wt.%, preferably from 0.01 to 0.1 wt.%, based on components A+B.
  • lubricants there come into consideration, for example, zinc, magnesium and calcium stearates as well as polyalkylene ether waxes.
  • polyester resins are known, for example, from EP 0 120 272 Al.
  • Vinyl ester resins the VE resins also referred to as phenacrylate resins (abbrev. PHA)
  • phenacrylate resins are reaction resins based on phenyl(ene) derivatives, such as, for example, ⁇ aromat. glycidyl ethers of phenols or epoxidised novolaks, whose mol. have been esterified by (meth) acrylic acid.
  • the so-called "vinyl ester” class of resins has for some years been recognized as useful for a wide range of resin applications, especially those demanding superior chemical resistance.
  • the resins are chemically the reaction products of epoxy resins and ethylenically unsaturated - ' products of epoxy resins.
  • Typical vinyl ester resins now commercially available include the EPOCRYL resins (marketed by Shell Chemical Company) , DERKANE 411 (marketed by Dow Chemicals Company) and CO-REZYN VE-8300 (marketed by Itnerplastic Company) .
  • the viscosity of the resin composition should be controlled so that the composition is fluid enough to allow easy application and good wetting of fillers and reinforcement, yet not so fluid that it drains from vertical surfaces to cause resin-starved areas in the shaped products.
  • excellent body and hold-up characteristics are very important if not critical to the procedure, especially during the shaping and curing steps.
  • the resin is typically dissolved in a vinyl monomer, e.g., styrene, whereupon it is shaped cured to produce shaped products. If, during the shaping and curing steps, the body and hold-up characteristics of the composition are such that outflow or running of the composition occurs when, for instance, the resin composition is applied onto a vertical surface for lining, the resin surface of the shaped product may be of uneven thickness and have diminished mechanical strength.
  • a vinyl monomer e.g., styrene
  • a composition of the present invention may comprise a comonomer, in order to facilitate handling, cure and to provide desired mechanical properties.
  • Suitable compatible comonomers include reactive, ethylenically unsaturated comonomers such as styrene, chlorostyrene, vinyltoluenes, methylstyrene, diallyl phthalate, triallyl cyanurate, acrylate esters, methacrylate esters and divinyl-benzene.
  • Styrene is the preferred compactible adjuvant.
  • the composition may also comprise a non-reactive diluent, such as acetone, where properties obtainable only with the neat resin are desired.
  • the vinyl ester resins used in the present invention may be any of those known in the art and may be prepared by an addition reaction between an epoxy resin and an ethylenically unsaturated monocarboxylic acid. Processes for preparing suitable vinyl ester resins are disclosed in U.S. Patent Specifications Nos. 3,256,226; 3,317,465; 3,345,401; 3,373,221; 3,377,406; 3,432,478; 3,548,030; 3,564,074; 3,634,542 and 3,637,518.
  • the reaction by means of which the vinyl ester resins used in the present invention are prepared is straightforward. It may be catalysed by suitable catalysts such as, for instance, tertiary amines, phosphines, alkalis or-onium salts.
  • suitable catalysts such as, for instance, tertiary amines, phosphines, alkalis or-onium salts.
  • the general equation for the reaction may be represented as follows:
  • R is, for instance, alkylene, cycloalkylene, arylene, arylalkylene, oxyarylene, oxyarylalkylene or cycloalkylene ester.
  • a substantial number of different vinyl esters combining different characteristics may be prepared by combining different epoxy resins with various unsaturated acids.
  • the variety of products may of course be even further extended, depending upon the selection of the unsaturated monomers which can be combined, and copolymerised, with the vinyl ester resin.
  • the vinyl ester resins which have so far achieved the greatest utility and which are therefore preferred for use in the present invention are the bisphenol-A (BPA) -epoxy based vinyl ester resins. These resins may be employed in the compositions of the present invention either with or without a co-reactive monomer such as styrene.
  • the resin composition of the present invention may also comprise catalysts, inhibitors, fillers, pigments and/or other known conventional additives.
  • compositions of the invention may be polymerised and cross-linked, using free radical generating initiators which are known in the art.
  • Polymerisation of the resin is by means of a true addition reaction and, typically, no by-products are formed.
  • Suitable initiators include peroxides, preferably organic peroxides such as benzoyl peroxides or methyl ethyl ketone peroxide, as well as other sources of free radicals.
  • photoinitiators which generate free radicals may also be used to initiate polymerisation of the composition of the present invention.
  • the initiator may be used with conventional accelerators or promoters such as, for instance, tertiary amines, e.g. dimethyl or diethyl aniline, and metallic soaps such as cobalt or manganese octoate or naphthenate.
  • Suitable methods include the hand lay-up method, the coldpress method, the bag method, the matched- die method, the filament-winding method and the continuous moulding method.
  • Acrylic resins may be cold- or heat-curable synthetic resins, which are obtained by homopolymerisation of (meth) acrylic acid esters (so-called pure-A. ) or their copolymerisation with, for example, styrene or vinyl esters.
  • Heat-curable acrylic resins additionally contain functional groups (hydroxy, hydroxymethyl, carboxy groups) via which crosslinking reactions can be carried out; they may be self- crosslinking or (for example after addition of aminoplastics or epoxy resins) crosslink by external means.
  • the solubility and mechanical properties of the acrylic resins can be varied widely via the choice of monomers.
  • Cured acrylic resins are generally transparent products which are resistant to UV light and do not discolour.
  • a cold-curing coating resin may have the following composition, for example:
  • (meth) acrylate from 50 to 100 wt.% methyl (meth) acrylate from 0 to 5 wt.% ethyl (meth) acrylate from 0 to 5 wt.%
  • a redox system which is to be kept separate, at least in respect of one component of the redox system, until polymerisation of the polymerisable constituents of the system, which redox system . contains an accelerator and a peroxidic catalyst or initiator in an amount sufficient for the cold curing of component A) , and
  • Mixed resins may be mixtures of polyester resins and vinyl esters and/or acrylic resins in order to achieve combinations of properties which are particularly advantageous from a commercial point of view.
  • the resins are mixed carefully with the silica, and the curing agent and, optionally, an accelerator are added thereto.
  • curing takes place at a temperature which may be markedly below room temperature, in the region of room temperature or in a temperature range markedly above room temperature.
  • the upper temperature limit is generally determined by the physico-chemical data of the resin, such as, for example, the vapour pressure of the monomers.
  • the duroplastics according to the invention which contain the structurally modified silica containing acrylic groups, may be liquid, pasty or in solid form.
  • pulverulent or fibrous filling materials such as:
  • Further additives may be:
  • silica used in accordance with the invention which contains methacrylic groups and has been prepared by flame hydrolysis and whose structure has been altered by mechanical after-treatment, brings about a number of technical advantages in the resins according to the invention and preparations prepared therefrom.
  • the thixotropic action is very low. That is of great benefit for the application and loss behaviour of coatings and adhesive preparations.
  • the acrylic-functional groups firmly bonded to the solid surface react during polymerisation of the reactive resin to form crosslinking sites, which impart to the end product a high degree of hardness, strength and elasticity.
  • the speed of the crosslinking reaction can be increased, so that coatings are more rapidly dust-dry and laminates can be removed from the mould earlier.
  • the processing of moulding compositions is improved, especially in the case of highly filled systems the reactivity of the silica according to the invention effects uniform through-curing of the moulding within a short time.
  • a particular advantage when using the silica according to the invention containing methacrylic groups and prepared by flame hydrolysis is also that no free alcohol forms in the preparation, as is unavoidable when using liquid silanes according to the prior art.
  • the alcohol released on in situ silanisation by hydrolysis reaction can give rise to a variety of faults during further processing of the resin preparations, such as acceleration or retardation of the crosslinking process.
  • the silanisation reaction requires a measurable period of time and/or the use of catalysts and/or heat as well as, optionally, measures for removing the alcohol that is formed and excess silane.
  • liquid or pasty resins of the silica according to the invention containing methacrylic groups and prepared by flame hydrolysis can have an advantageous effect on the settling behaviour of other fillers, predominantly those having a relatively coarse grain size, even if that effect is not to the fore.
  • 100 parts by weight of the resin from Comparative Example 1 are mixed with the aid of a dissolver with 15 parts by weight of a silica which is coated with trimethylsilyl groups and has been prepared by flame hydrolysis and which has a specific surface area of 173 square metres and a carbon content, determined by analysis, of 3.4 wt.%, and whose structure has been altered by mechanical after-treatment.
  • the viscosity is determined at 23°C by brief de-aeration in a low-pressure cabinet.
  • the pasty composition so obtained has a marked flow limit, but is spreadable.
  • 1 wt.% of the 33 % MEK peroxide solution is added thereto, and heating is carried out at 80°C for a period of 15 minutes in a rectangular mould. During that time, the preparation cures fully and is removed from the mould as a translucent sheet.
  • Example 1 (prior art):
  • a silica which contains methacrylic groups and has been prepared by flame hydrolysis and which has a specific surface area of 160 m 2 /g, a mean particle size of 12 nanometres and a carbon content of 5 % are mixed with the aid of a dissolver with 100 parts by weight of an unsaturated styrene-containing isophthalic acid polyester resin.
  • the admixed air is removed by brief de-aeration in a low-pressure cabinet.
  • the viscosity is determined at 23°C with the aid of a cone/plate rheometer.
  • the composition has a flow limit, but is very readily spreadable. 1 wt.% of the 33 % MEK peroxide solution is added thereto, and heating is carried out at 80°C for a period of 15 minutes in a rectangular mould. During that time, the composition cures fully and is removed from the mould as a translucent sheet.
  • Example 1 1 wt.% of the 33 % MEK peroxide solution is added as in Example 1 to 100 parts by weight of an unsaturated styrene-containing brominated vinyl ester resin; the mixture is shaped to form a sheet and cured.
  • Example 1 100 parts by weight of an unsaturated styrene-containing brominated vinyl ester resin are mixed as in Example 1 with 15 parts by weight of a silica which is coated with trimethylsilyl groups and has been prepared by flame hydrolysis and which has a specific surface area of 173 m 2 and whose structure has been altered by mechanical after- treatment.
  • the composition is readily flowable.
  • a silica which contains methacrylic groups and has been prepared by flame hydrolysis and which has a specific surface area of 160 m 2 /g, a mean particle size of 12 nanometres and a carbon content of 5 %, and whose structure has been altered by mechanical after- treatment, are mixed with 100 parts by weight of an unsaturated styrene-containing brominated vinyl resin. There is no noticeable flow limit, the composition can be poured very readily. It is mixed with 1 wt.% of the 33 % MEK peroxide solution, de-aerated, and shaped to form a sheet and cured as in Example 1.
  • a silica which contains trimethylsilyl groups and has been prepared by trimethylsilyl flame hydrolysis and which has a specific surface area of 173 m 2 /g, a mean particle size of 12 nanometres and a carbon content of 3.4 % are mixed with 100 parts by weight of the PMMA resin from Comparative Example 5.
  • the preparation has a markedly increased flow limit in comparison with Comparative Example 5.
  • -It is mixed with 3 wt.% of the curing agent, poured out to form a sheet and cured at room temperature. The surface has a slight residual tackiness.
  • Example 3 (according to the invention):
  • the flow limit is increased only slightly as compared with the unfilled resin (Comparative Example 5) .
  • the mixture is then mixed with 3 parts by weight of the curing agent, poured out to form a thin sheet and cured at room temperature. After 16 hours, the sheet has cured through. The surface is non-tacky.
  • both silicas bring about an increase in hardness and modulus in the crosslinked resin preparations.
  • the silica modified with methacrylic groups is distinguished by a substantially more ' pronounced action, which leads in Example 2 to a noticeable brittleness of the resin.
  • the person skilled in the art will recognise the potential for making a saving here and will reduce the dosage or use a more flexible base resin.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

L'invention concerne des duroplastiques liquides renforcés préparés selon un procédé qui consiste à ajouter, aux duroplastiques, une silice préparée par pyrogénie modifiée en surface au moyen de silanes contenant des groupes méthacryliques.
PCT/EP2002/007276 2002-07-02 2002-07-02 Duroplastiques liquides WO2004005393A1 (fr)

Priority Applications (6)

Application Number Priority Date Filing Date Title
CN02829252A CN100575403C (zh) 2002-07-02 2002-07-02 液体硬质塑料
PCT/EP2002/007276 WO2004005393A1 (fr) 2002-07-02 2002-07-02 Duroplastiques liquides
AU2002321158A AU2002321158A1 (en) 2002-07-02 2002-07-02 Liquid duroplastics
JP2004518475A JP2005531672A (ja) 2002-07-02 2002-07-02 液状デュロプラスチック
EP02754810A EP1517949A1 (fr) 2002-07-02 2002-07-02 Duroplastiques liquides
TW092117450A TW200401798A (en) 2002-07-02 2003-06-26 Liquid duroplastics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/EP2002/007276 WO2004005393A1 (fr) 2002-07-02 2002-07-02 Duroplastiques liquides

Publications (1)

Publication Number Publication Date
WO2004005393A1 true WO2004005393A1 (fr) 2004-01-15

Family

ID=30011028

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2002/007276 WO2004005393A1 (fr) 2002-07-02 2002-07-02 Duroplastiques liquides

Country Status (6)

Country Link
EP (1) EP1517949A1 (fr)
JP (1) JP2005531672A (fr)
CN (1) CN100575403C (fr)
AU (1) AU2002321158A1 (fr)
TW (1) TW200401798A (fr)
WO (1) WO2004005393A1 (fr)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006053632A3 (fr) * 2004-11-18 2006-06-29 Degussa Silice hydrophobe et son utilisation dans du caoutchouc de silicone
EP1783556A2 (fr) 2004-08-19 2007-05-09 ASML Netherlands B.V. Appareil lithographique et procédé de fabrication d'un dispositif semiconducteur
WO2008141929A1 (fr) * 2007-05-22 2008-11-27 Evonik Degussa Gmbh Adhésifs
WO2013156337A1 (fr) 2012-04-20 2013-10-24 Evonik Degussa Gmbh Adhésif renforcé à base de résine époxy

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3328339A (en) * 1963-08-28 1967-06-27 Monsanto Co Reinforced plastics containing base treated, calcined particulate fillers and organosilane coupling agents
US20020077381A1 (en) * 2000-10-21 2002-06-20 Stephanie Frahn Radiation-curing coating systems
US20020077388A1 (en) * 2000-10-21 2002-06-20 Jurgen Meyer Functionalized, structurally modified silicas
US20020077407A1 (en) * 2000-10-21 2002-06-20 Jurgen Meyer Functionalized silicas

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3328339A (en) * 1963-08-28 1967-06-27 Monsanto Co Reinforced plastics containing base treated, calcined particulate fillers and organosilane coupling agents
US20020077381A1 (en) * 2000-10-21 2002-06-20 Stephanie Frahn Radiation-curing coating systems
US20020077388A1 (en) * 2000-10-21 2002-06-20 Jurgen Meyer Functionalized, structurally modified silicas
US20020077407A1 (en) * 2000-10-21 2002-06-20 Jurgen Meyer Functionalized silicas

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1783556A2 (fr) 2004-08-19 2007-05-09 ASML Netherlands B.V. Appareil lithographique et procédé de fabrication d'un dispositif semiconducteur
WO2006053632A3 (fr) * 2004-11-18 2006-06-29 Degussa Silice hydrophobe et son utilisation dans du caoutchouc de silicone
US8071215B2 (en) 2004-11-18 2011-12-06 Evonik Degussa Gmbh Hydrophobic silica and its use in silicone rubber
WO2008141929A1 (fr) * 2007-05-22 2008-11-27 Evonik Degussa Gmbh Adhésifs
US8173737B2 (en) 2007-05-22 2012-05-08 Evonik Degussa Gmbh Adhesives
WO2013156337A1 (fr) 2012-04-20 2013-10-24 Evonik Degussa Gmbh Adhésif renforcé à base de résine époxy

Also Published As

Publication number Publication date
TW200401798A (en) 2004-02-01
EP1517949A1 (fr) 2005-03-30
CN1633467A (zh) 2005-06-29
JP2005531672A (ja) 2005-10-20
CN100575403C (zh) 2009-12-30
AU2002321158A1 (en) 2004-01-23

Similar Documents

Publication Publication Date Title
Fink Reactive polymers: fundamentals and applications: a concise guide to industrial polymers
AU748828B2 (en) Polymer composite and a method for its preparation
JP3730317B2 (ja) 人工大理石用熱硬化性樹脂組成物および人工大理石
AU2008301029B2 (en) Low VOC thermosetting composition of polyester acrylic resin for gel coat
CA1065533A (fr) Composition pour le moulage et methode de fabrication
CA2049895C (fr) Revetement dans le moule a durcissement rapide
EP0742249B1 (fr) Revêtement pour améliorer les propriétés de surface de matières plastiques renforcées par de la fibre de verre
US4172102A (en) Low-shrink unsaturated polyester molding compositions
WO2005113632A1 (fr) Resine vinylester hors poisse a faible cov
WO2020128906A1 (fr) Composition présentant une résine de polyester, un acrylate et un ester vinylique et son procédé d'utilisation
JP2943148B2 (ja) 熱硬化性樹脂組成物
WO2019016704A1 (fr) Composition comprenant une résine polyester liquide et son procédé d'utilisation
WO2004005393A1 (fr) Duroplastiques liquides
JP2003327845A (ja) 耐衝撃性成形材料組成物
US5554666A (en) Photocurable compositions
JP2013543032A (ja) 不粘着性コーティング製造用組成物
JP3263164B2 (ja) 塗装性に優れた自動車外装部品の成形品用不飽和ポリエステル樹脂組成物及び成形材料、並びに塗装性に優れた自動車外装部品の成形品
KR20120136883A (ko) 시트 몰딩 컴파운드 성형용 전도성 불포화 폴리에스테르 수지 조성물, 이의 제조방법 및 이를 포함하는 열경화 수지 조성물
KR20050024456A (ko) 액상 듀로플라스틱 물질
CN110016107B (zh) 固化性树脂组合物
JP7181074B2 (ja) 硬化性樹脂組成物及び３成分型硬化性樹脂組成物、それらの硬化物、並びに耐食床の製造方法
JPS61126141A (ja) 成形組成物
JP3795538B2 (ja) 熱硬化性樹脂組成物およびその用途
JP2850234B2 (ja) 樹脂組成物
WO2020128904A1 (fr) Composition comprenant une résine de polyester et un ester vinylique et procédé d'utilisation de celle-ci

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ OM PH PL PT RO RU SD SE SG SI SK SL TJ TM TN TR TT TZ UA UG US UZ VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR IE IT LU MC NL PT SE SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 2002754810

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 20028292529

Country of ref document: CN

WWE Wipo information: entry into national phase

Ref document number: 1020047021708

Country of ref document: KR

WWE Wipo information: entry into national phase

Ref document number: 2004518475

Country of ref document: JP

WWP Wipo information: published in national office

Ref document number: 1020047021708

Country of ref document: KR

WWP Wipo information: published in national office

Ref document number: 2002754810

Country of ref document: EP

WWR Wipo information: refused in national office

Ref document number: 2002754810

Country of ref document: EP

WWW Wipo information: withdrawn in national office

Ref document number: 2002754810

Country of ref document: EP