Patent Application
20100015437
The invention provides a titanium-dioxide-containing composite, a method for its production and the use of this composite.
From the application of conventional fillers and pigments, also known as additives, in polymer systems it is known that the nature and strength of the interactions between the particles of the filler or pigment and the polymer matrix influence the properties of a composite. Through selective surface modification the interactions between the particles and the polymer matrix can be modified and hence the properties of the filler and pigment system in a polymer matrix, hereinafter also referred to as a composite. A conventional type of surface modification is the functionalisation of the particle surfaces using alkoxyalkylsilanes. The surface modification can serve to increase the compatibility of the particles with the matrix. Furthermore, a binding of the particles to the matrix can also be achieved through the appropriate choice of functional groups.
A second possibility for improving the mechanical properties of polymer materials is the use of ultrafine particles. U.S. Pat. No. 6,667,360 discloses polymer composites containing 1. to 50 wt. % of nanoparticles having particle sizes from 1 to 100 nm. Metal oxides, metal sulfides, metal nitrides, metal carbides, metal fluorides and metal chlorides are suggested as nanoparticles, the surface of these particles being unmodified. Epoxides, polycarbonates, silicones, polyesters, polyethers, polyolefines, synthetic rubber, polyurethanes, polyamide, polystyrenes, polyphenylene oxides, polyketones and copolymers and blends thereof are cited as the polymer matrix. In comparison to the unfilled polymer, the composites disclosed in U.S. Pat. No. 6,667,360 are said to have improved mechanical properties, in particular tensile properties and scratch resistance values.
A further disadvantage of the filler-modified composites described in the prior art is their inadequate mechanical properties for many applications.
An object of the present invention is to overcome the disadvantages of the prior art.
An object of the invention is in particular to provide a composite which has markedly improved values for flexural modulus, flexural strength, tensile modulus, tensile strength, crack toughness, fracture toughness, impact strength and wear rates in comparison to prior art composites.
Improved mechanical properties allow thinner components to be produced. This can make a decisive contribution to reducing weight in the automotive and aerospace sector. Applications include, for example, bumpers or interior trim in trains and aircraft made from thermoset moulding compositions. Adhesives require high tensile strength values above all. Applications for elastomeric plastics, based for example on polymers such as styrene-butadiene rubber (SBR), include inter alia seals and vibration dampers.
Surprisingly the object was achieved with composites according to the invention having the features of the main claim. Preferred embodiments are characterised in the sub-claims.
Surprisingly the mechanical and tribological properties of polymer composites were greatly improved even with the use of precipitated, surface-modified titanium dioxide having crystallite sizes d50 of less than 350 nm (measured by the Debye-Scherrer method). Astonishingly, a physical bond between the particles and matrix has a particularly favourable effect on improving the mechanical and tribological properties of the composite.
The composite according to the invention contains a polymer matrix and 0.1 to 60 wt. % of precipitated titanium dioxide particles, with average crystallite sizes d50 of less than 350 nm (measured by the Debye-Scherrer method). The crystallite size d50 is preferably less than 200 nm, particularly preferably 3 to 50 nm. The titanium dioxide particles can have a spherical or bar-shaped morphology.
The composites according to the invention can also contain components known per se to the person skilled in the art, for example mineral fillers, glass fibres, stabilisers, process additives (also known as protective systems, for example dispersing aids, release agents, antioxidants, anti-ozonants, etc.), pigments, flame retardants (e.g. aluminium hydroxide, antimony trioxide, magnesium hydroxide, etc.), vulcanisation accelerators, vulcanisation retarders, zinc oxide, stearic acid, sulfur, peroxide and/or plasticisers.
A composite according to the invention can for example additionally contain up to 80 wt. %, preferably 10 to 80 wt. %, of mineral fillers and/or glass fibres, up to 10 wt. %, preferably 0.05 to 10 wt. %, of stabilisers and process additives (e.g. dispersing aids, release agents, antioxidants, etc.), up to 10 wt. % of pigment and up to 40 wt. % of flame retardant (e.g. aluminium hydroxide, antimony trioxide, magnesium hydroxide, etc.).
A composite according to the invention can for example contain 0.1 to 60 wt. % of titanium dioxide, 0 to 80 wt. % of mineral fillers and/or glass fibres, 0.05 to 10 wt. % of stabilisers and process additives (e.g. dispersing aids, release agents, antioxidants, etc.), 0 to 10 wt. % of pigment and 0 to 40 wt. % of flame retardant (e.g. aluminium hydroxide, antimony trioxide, magnesium hydroxide, etc.).
The polymer matrix can consist of an elastomer or a thermoset. Examples of elastomers are natural rubber (NR), isoprene rubber (IR), butyl rubber (CIIR, BIIR), butadiene rubber (BR), styrene-butadiene rubber (SBR), acrylonitrile-butadiene rubber (NBR), bromobutyl rubber (BIIR), styrene-butadiene-isoprene rubber (SBIR), chloroprene rubber (CR), chlorosulfonated polyethylene rubber (CSM), hydrogenated NBR rubber (HNBR), polymethylsiloxane-vinyl rubber (VMQ), acrylate-ethylene rubber (AEM), acrylate rubber (ACM), fluoro rubber (FKM), fluorosilicone rubber (FVMQ), thermoplastic elastomers (TPE), thermoplastic elastomers (TPE) based on polyamide (TPA), based on copolyesters (TPC), based on olefins (TPO), based on styrene (TPS), based on polyurethane (TPU), based on vulcanised rubber (TPV) or mixtures of at least two of these plastics. Suitable thermosets are, for example, unsaturated polyester resins (UP), phenolic resins, melamine resins, formaldehyde moulding compositions, vinyl ester resins, diallyl phthalate resins, silicone resins or urea resins. UP resins are particularly suitable thermosets.
The composite according to the invention can contain 0.1 to 60 wt. % of precipitated, surface-modified titanium dioxide, 0 to 80 wt. % of mineral fillers and/or glass fibres, 0.05 to 10 wt. % of stabilisers and process additives (e.g. dispersing aids, release agents, antioxidants, etc.), 0 to 10 wt. % of pigment and 0 to 40 wt. % of flame retardant (e.g. aluminium hydroxide, antimony trioxide, magnesium hydroxide, etc.).
According to the invention ultrafine titanium dioxide particles having an inorganic and/or organic surface modification can be used.
The inorganic surface modification of the ultrafine titanium dioxide typically consists of compounds containing at least two of the following elements: aluminium, antimony, barium, calcium, cerium, chlorine, cobalt, iron, phosphorus, carbon, manganese, oxygen, sulfur, silicon, nitrogen, strontium, vanadium, zinc, tin and/or zirconium compounds or salts. Sodium silicate, sodium aluminate and aluminium sulfate are cited by way of example.
The inorganic surface treatment of the ultrafine titanium dioxide takes place in an aqueous slurry. The reaction temperature should. preferably not exceed 50° C. The pH of the suspension is set to pH values in the range above 9, using NaOH for example. The post-treatment chemicals (inorganic compounds), preferably water-soluble inorganic compounds such as, for example, aluminium, antimony, barium, calcium, cerium, chlorine, cobalt, iron, phosphorus, carbon, manganese, oxygen, sulfur, silicon, nitrogen, strontium, vanadium, zinc, tin and/or zirconium compounds or salts, are then added whilst stirring vigorously. The pH and the amounts of post-treatment chemicals are chosen according to the invention such that the latter are completely dissolved in water. The suspension is stirred intensively so that the post-treatment chemicals are homogeneously distributed in the suspension, preferably for at least 5 minutes. In the next step the pH of the suspension is lowered. It has proved advantageous to lower the pH slowly whilst stirring vigorously. The pH is particularly advantageously lowered to values from 5 to 8 within 10 to 90 minutes. This is followed according to the invention by a maturing period, preferably a maturing period of approximately one hour. The temperatures should preferably not exceed 50° C. The aqueous suspension is then washed and dried. Possible methods for drying ultrafine, surface-modified titanium dioxide include spray-drying, freeze-drying and/or mill-drying, for example. Depending on the drying method, a subsequent milling of the dried powder may be necessary. Milling can be performed by methods known per se.
According to the invention the following compounds are particularly suitable as organic surface modifiers: polyethers, silanes, polysiloxanes, polycarboxylic acids, fatty acids, polyethylene glycols, polyesters, polyamides, polyalcohols, organic phosphonic acids, titanates, zirconates, alkyl and/or aryl sulfonates, alkyl and/or aryl sulfates, alkyl and/or aryl phosphoric acid esters.
Organically surface-modified titanium dioxide can be produced by methods known per se. One option is surface modification in an aqueous or solvent-containing phase. Alternatively the organic component can be applied to the surface of the particles by direct spraying followed by mixing/milling.
According to the invention suitable organic compounds are added to a titanium dioxide suspension whilst stirring vigorously and/or during a dispersion process. During this process the organic modifications are bound to the particle surface by chemisorption/physisorption.
Suitable organic compounds are in particular compounds selected from the group of alkyl and/or aryl sulfonates, alkyl and/or aryl sulfates, alkyl and/or aryl phosphoric acid esters or mixtures of at least two of these compounds, wherein the alkyl or aryl radicals can be substituted with functional groups. The organic compounds can also be fatty acids, optionally having functional groups. Mixtures of at least two such compounds can also be used.
The following can be used by way of example: alkyl sulfonic acid salt, sodium polyvinyl sulfonate, sodium-N-alkyl benzenesulfonate, sodium polystyrene sulfonate, sodium dodecyl benzenesulfonate, sodium lauryl sulfate, sodium cetyl sulfate, hydroxylamine sulfate, triethanol ammonium lauryl sulfate, phosphoric acid monoethyl monobenzyl ester, lithium perfluorooctane sulfonate, 12-bromo-1-dodecane sulfonic acid, sodium-10-hydroxy-1-decane sulfonate, sodium-carrageenan, sodium-10-mercapto-1-cetane sulfonate, sodium-16-cetene(1) sulfate, oleyl cetyl alcohol sulfate, oleic acid sulfate, 9,10-dihydroxystearic acid, isostearic acid, stearic acid, oleic acid.
The organically modified titanium dioxide can either be used directly in the form of the aqueous paste or can be dried before use. Drying can be performed by methods known per se. Suitable drying options are in particular the use of convection-dryers, spray-dryers, mill-dryers, freeze-dryers and/or pulse-dryers. Other dryers can also be used according to the invention, however. Depending on the drying method, a subsequent milling of the dried powder may be necessary. Milling can be performed by methods known per se.
According to the invention the surface-modified titanium dioxide particles optionally have one or more functional groups, for example one or more hydroxyl, amino, carboxyl, epoxy, vinyl, methacrylate and/or isocyanate groups, thiols, alkyl thiocarboxylates, di- and/or polysulfide groups.
Surface modifiers which are bound to the titanium dioxide particles by one functional group and which interact with the polymer matrix via another functional group are preferred.
The surface modifiers can be chemically and/or physically bound to the particle surface. The chemical bond can be covalent or ionic. Dipole-dipole or van der Waals bonds are possible as physical bonds. The surface modifiers are preferably bound by means of covalent bonds or physical dipole-dipole bonds.
According to the invention the surface-modified titanium dioxide particles have the ability to form a partial or complete chemical and/or physical bond with the polymer matrix via the surface modifiers. Covalent and ionic bonds are suitable as chemical bond types. Dipole-dipole and van der Waals bonds are suitable as physical bond types.
In order to produce the composite according to the invention a masterbatch can preferably be produced first, which preferably contains 5 to 80 wt. % of titanium dioxide. This masterbatch can then either be diluted with the crude polymer only or mixed with the other constituents of the formulation and optionally dispersed again.
In order to produce the composite according to the invention a method can also be chosen wherein the titanium dioxide is first incorporated into organic substances, in particular into amines, polyols, styrenes, formaldehydes and moulding compositions thereof, vinyl ester resins, polyester resins or silicone resins, and dispersed. These organic substances with added titanium dioxide can then be used as the starting material for production of the composite.
Conventional dispersing methods, in particular using melt extruders, high-speed mixers, triple roll mills, ball mills, bead mills, submills, ultrasound or kneaders, can be used to disperse the titanium dioxide in the masterbatch. The use of submills or bead mills with bead diameters of d<1.5 mm is particularly advantageous.
The composite according to the invention surprisingly has outstanding mechanical and tribological properties. In comparison to the unfilled polymer the composites according to the invention have markedly improved values for flexural modulus, flexural strength, tensile modulus, tensile strength, crack toughness, fracture toughness, impact strength and wear rates.
The invention provides in detail:
The invention is illustrated by means of the examples below, without being limited thereto.
The organically post-treated and surface-modified titanium dioxide is dispersed in the UP resin Palapreg P17-02 in a concentration of 25 wt. % using a bead mill until the fineness measured on a Hegmann gauge is less than 5 μm.
The inorganically post-treated and surface-modified titanium dioxide can be produced in the following way, for example:
3.7 kg of a 6.5 wt. % aqueous suspension of ultrafine titanium dioxide particles having average primary particle diameters d50 of 14 nm (result of TEM analyses) are heated to a temperature of 40° C. whilst stirring. The pH of the suspension is adjusted to 12 using 10% sodium hydroxide solution. 14.7 ml of an aqueous sodium silicate solution (284 g SiO2/l), 51.9 ml of an aluminium sulfate solution (with 75 g Al2O3/I) and 9.7 ml of a sodium aluminate solution (275 g Al2O3/I) are added simultaneously to the suspension whilst stirring vigorously and keeping the pH at 12.0. The suspension is homogenised for a further 10 minutes whilst stirring vigorously. The pH is then slowly adjusted to 7.5, preferably within 60 minutes, by adding a 5% sulfuric acid. This is followed by a maturing time of 10 minutes, likewise at a temperature of 40° C. The reaction suspension is filtered and the resulting filter cake is washed with demineralised water to a conductivity of less than 100 μS/cm. This filter cake is dispersed to produce a suspension having a solids content of 20 wt. %. 15 g of 3-methacryloxypropyl-trimethoxysilane are added slowly to the suspension whilst dispersing with the high-speed mixer. The suspension is then dispersed with the high-speed mixer for a further 20 minutes and dried in a spray-dryer.
This dispersion based on the material weights specified in Table 1 is stirred with the additional resin Palapreg H814-01 and the additives in a high-speed mixer (mixer disc: diameter 30 mm) at 1500 rpm in a 180 ml plastic beaker and the necessary amount of fillers is added slowly whilst increasing the speed. On completion of the addition of fillers, the mixture is dispersed for 3 minutes at 6500 rpm.
The necessary amount of glass fibres is added to the crude composition and folded in with the aid of a spatula. This mixture is homogenised in a kneader for a further 3 minutes at 50 rpm. The resulting composition is carefully spread into a mould, which is impregnated with release agent and has 12 recesses measuring 80×15×4 mm3, and the surface is smoothed. The lower press platen of the mould is a Teflon plate, the upper press platen is a polished, chrome-plated metal plate. These three plates together with the protective paper are introduced into the press, which has been pre-heated to 150° C., and heated for one minute at 150° C. (with the press closed under normal pressure) and then the plates are press-moulded under a pressure of 100 bar at 150° C. After press-moulding the plates are left to cool and the specimens are pushed out of the mould.
The specimens from Example 1 are examined in 3-point bending tests as defined in DIN EN ISO 178 and in impact strength tests as defined in DIN EN ISO 179. The results are set out in Table 2.
The composites according to the invention exhibit greatly improved properties in comparison to the pure resin.
| Number | Date | Country | Kind |
|---|---|---|---|
| 102006039856.4 | Aug 2006 | DE | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP07/58896 | 8/27/2007 | WO | 00 | 5/28/2009 |
