Title of Invention	AN ADHESIVE COMPOSITION FOR THE PRODUCTION OF THERMOSOTS.
Abstract	Adhesive composition for the production of thermosests, the composition being able to be heated by means of an electrical field, magnetic field, electromagnetic field, alternating electrical field, alternating magnetic field or alternating electromagnetic field and containing a polymer, a polymer mixture or a reaction resin, and crosslinking agent particles, wherein the crosslinking agent particles comprise filler particles that are ferromagnetic, ferrimagnetic, superparamagnetic or paramagnetic and crosslinking agent units chemically bound to these filler particles.

Title of Invention

AN ADHESIVE COMPOSITION FOR THE PRODUCTION OF THERMOSOTS.

Abstract

Adhesive composition for the production of thermosests, the composition being able to be heated by means of an electrical field, magnetic field, electromagnetic field, alternating electrical field, alternating magnetic field or alternating electromagnetic field and containing a polymer, a polymer mixture or a reaction resin, and crosslinking agent particles, wherein the crosslinking agent particles comprise filler particles that are ferromagnetic, ferrimagnetic, superparamagnetic or paramagnetic and crosslinking agent units chemically bound to these filler particles.

Full Text	Description Technical Field The present invention relates to an adhesive composition which contains inductively heatable filler particles, and to its use and a process for its curing. The invention also relates to an adhesive composite that contains a hardened layer of the adhesive composition, a process for the thermal dissociation of the hardened adhesive composition, and the use of this process. Prior Art Adhesive bonds, i.e. in particular bonded joints, coatings, laminates or cast structural parts are designed so that they can be produced under mild conditions, are resistant for as long as possible and have the highest possible strengths. High strengths mean that, in the case of a repair or recycling, a dissociation of the adhesive bond can be carried out only under extreme conditions, such as for example the action of strong forces or high temperatures. Bonded joints based on hard adhesives are generally dissociable, but are not suitable for transmitting the high forces necessary for structural bonded joints. The dissociation of high-strength bonded joints is generally accomplished by the use of mechanical energy or chemical agents. The latter have the disadvantage that they cause a high environmental pollution and also that the penetration of the agents into the gluelines of structural bonded joints that are stable over the long term takes far too long. DE 43 28 108 A describes the dissociation of floor coverings by means of microwave energy. For this purpose a contact adhesive is used that is electrically conducting and is filled with copper powder or aluminium powder. These fillers have the disadvantage that the particles have sizes of a few micrometres and larger. This leads to a non-uniform heating of the contact adhesive. DE 199 61 940 Al describes adhesives for dissociable bonded joints that contain thermally activatable substances that release gaseous compounds when they decompose, which then destroy the bonded joints. This process has the disadvantage that in order to separate the composite, the whole structural part or the joined parts and the adhesive have to be heated. This is associated with a high energy expenditure. Furthermore it is not possible to achieve a locally restricted separation of the structural part or of the joined part. DE 199 51 599 Al and DE 199 24 138 Al describe adhesives for dissociable bonded joints and bonded joints produced therewith, that contain externally excitable nanofillers. The dissociation of the bonded joints is achieved by introducing the joints into an alternating electrical, magnetic or electromagnetic field, whereby the nanofillers and the surrounding adhesive are heated. This process has the disadvantage however that it leads to the heating of the whole adhesive, also at places at which no heating is necessary or desirable, since the excitable nanofillers are also contained in places in the adhesive or primer where heating is not necessary in order to achieve the desired dissociation of the bonded joint. Furthermore high temperatures are required to separate high-strength bonded joints since chemical bonds have to be broken in order to break down the composite. The described processes furthermore have the disadvantage that a non-specific thermal decomposition of the adhesive and/or primer occurs when separating high-strength bonded joints. Such processes are therefore unsuitable in particular for thermosets. The production of resistant, high-strength adhesive Joints is normally carried out thermally or photochemically. The conventional processes for producing adhesive bonded joints have the disadvantage however that the whole structural part has to be heated in order to cure the adhesive. As a result the process is enerqy intensive and time-consuming WO 99/03306 and 0. Hahn, A. Kaimann in Adhasion - Kleben und Dichten, 10/2001, pp. 35-38 describe a process for the inductive curing of adhesive joints. In this case adhesives that contain inductively activatable fillers are introduced into an electromagnetic field, whereby the inductively activatable fillers are heated and the hardening of the adhesive surrounding the fillers can take place. These processes have the disadvantage however that the inductively activatable substances are not uniformly distributed over the adhesive and accordingly there is an inhomogeneous heating of the adhesive. As a result, the strength of such adhesive joints is limited. The processes furthermore have the disadvantage that a demixing (separation) may occur in the adhesive during the inductive heating process and the distribution of the thermally activatable substances in the adhesive becomes even more irregular. Outline of the Invention The object of the present invention is to overcome the disadvantages of the prior art and to provide an adhesive composition that can be hardened under mild conditions to form a resistant, high-strength adhesive joint. A further object of the present invention is to provide a process for dissociating such adhesive joints without the long-term resistance of the adhesive joint inevitably suffering thereby. These objects are achieved by the adhesive composition the process for their curing the adhesive composite and the process for the thermal dissociation of the hardened adhesive composition. Uses of the adhesive composition and of the process for dissociating the hardened adhesive composition are mentioned in details in the specification. The subclaims disclose advantageous modifications. It was found that adhesive compositions that contain a polymer, a polymer mixture or a reaction resin, as well as particles of crosslinking agent, can be heated by means of an electrical field, magnetic field, electromagnetic field, alternating electrical field, alternating magnetic field or alternating electromagnetic field. The particles of crosslinking agent consist in this connection of filler particles that are metallic, ferromagnetic, ferromagnetic, superparamagnetic or paramagnetic, as well as crosslinking agent units that are chemically bound to the filler particles. A chemical reaction between the crosslinking agent unit anc the polymer or the polymer mixture is triggered by inductive heating of the particles of crosslinking agent, whereby a polymer network is formed. Adhesive compositions within the meaning of the present invention include in particular adhesives, paints, primers, casting compositions, sealants and laminating resins. In particular bonded joints, painted structural parts or structural parts provided with a primer, cast structural parts, sealed structural parts or polymer laminates are thereby formed by curing these adhesive compositions. As polymers, polymer mixtures and reaction resins within the meaning of the present invention there may be used all polymers, polymer mixtures and reaction resins that are considered suitable for the aforementioned applications. Preferred are crosslinked polymers, particularly preferably polymers or reaction resins from which structural or semi-structural joints can be produced. In particular epoxide resins, polyurethanes, acrylates, phenol resins, polysulfides or melamine resins are suitable. According to the invention the filler particles are chemically bound to the crosslinking agent component. This chemical bonding may be of an ionic, co-ordinative or covalent nature. Van-der-Waals interactions for example are also included under this heading. In order to produce the chemical bonds according to the invention it is advantageous if the surfaces of the filler particles are surface-modified, i.e. if they carry functional groups on their surface that can readily react with functional groups of the crosslinking agent unit. The crosslinking agent unit for its part carries at least one functional group that on heating can undergo crosslinking reactions with the polymer, the polymer mixture or the reactive resin. The heating may in this connection be accomplished either inductively or also in a conventional way. Suitable functional groups that undergo crosslinking reactions include for example epoxide, amino, thiol, alcohol, acrylate, methacrylate or vinyl groups. Chemical groups bound to the crosslinking agent unit that can react with the filler surface are in particular alkoxysilanes, alkoxy titanates and alkoxy zirconates. These lead to a bonding to the normally metallic or oxidic surface of the filler particles. Filler particles consisting of inductively excitable materials in the interior of the particles as well as of a particle surface predominantly of silicon dioxide are particularly preferred. They may be used in spherical or aggregated form. The predominantly spherical filler particles with a core-shell structure (see Fig. 1A, Fig. 2A) can be obtained for example via sol-gel processes or from the reaction of nanoscale iron oxide with sodium silicate; the aggregated filler particles with a silicon dioxide surface (Fig. 1B, Fig. 2B) are preferably obtained by means of gas phase synthesis. These particles are hereinafter termed composite particles. These composite particles consist of aggregates that exhibit the characteristic "sinter neck"; multiple inclusions or domains of the inductively excitable material are found distributed in the interior of the aggregates, while on the surface the composite particles consist largely of silicon dioxide. Particles with silicon dioxide on the surface have a high long-term resistance, with respect to moisture, of the bond between the crosslinking agent unit and the filler particle surface and react rapidly with the aforementioned chemical groups. Furthermore, the silicon dioxide layer protects the inductively excitable components against chemical attack by constituents of the formulation. The crosslinking agent particles according to the invention can be used for example as crosslinking agents for epoxide resins. This epoxide resin may for example be a bisphenol A diglycidyl ether hardened with a diamine. By using such crosslinking agent particles a thermoset is obtained that can be subjected to high chemical and thermal stress. An individual crosslinking agent particle with epoxide groups is shown diagrammatically by way of example in Fig. 1A. The filler particles may also be present in the form of agglomerates, as shown in Fig. 2A. Fig. 2A shows diagrammatically a section from an agglomerate of iron oxide particles in a silicon dioxide matrix. The adhesive compositions according to the invention have the advantage that the distribution of the filler particles is such that they are located only at those places where their action is necessary, namely in the crosslinking agent particles. Compared to the previously known adhesive compositions, the filler particles are in this case in direct (i.e. molecular or almost molecular) contact at those places at which their effect is to be manifested. In this way a non-specific heating of the whole polymer is avoided during inductive heating. The adhesive compositions according to the invention may therefore be inductively hardened under mild conditions. In addition the adhesive compositions according to the invention have the advantage that adhesive joints produced therefrom can also be inductively and cleanly re-separated, with savings in time and energy, without having to add substances that facilitate a separation. Here too the heating takes place selectively on a molecular level at the site at which the bonds are to be broken. This has the advantage that the whole polymer is not destroyed, as would be the case for example if it were heated with a welding torch or laser. A non-selective thermal decomposition of the polymer can thereby be avoided. Naturally, a lower induction output, i.e. for example a lower output of the high-frequency generator, is necessary for the crosslinking or curing than for the separation of the adhesive joint. According to the invention, in particular adhesive compositions are suitable that have a content of crosslinking agent particles of 0.1 to 80%, preferably 0.5 to 40% and particularly preferably 1% to 30%. By increasing the content of crosslinking agent particles or crosslinking agent units, a higher degree of crosslinking and thus a higher strength is achieved-. Advantageously the crosslinking agent particles have an average primary particle size, i.e. an average primary particles diameter, of less than 1000 nm, preferably less than 500 nm and particularly preferably between 2 nm and 100 nm. A uniform crosslinking of the adhesive composition according to the invention is achieved in this way. Furthermore, such small particle sizes are most suitable from the point of view of energy economy. The filler particles according to the invention may be present in an agglomerated state if the dispersion quality is insufficient. The crosslinking agent particles preferably comprise at least three functional groups having a crosslinking action, a thermoset thereby being formed. A thermoset is then generally obtained if three chemical groups (polymer systems curing by polycondensation or by polyaddition) or possibly even two chemical groups (polymer systems curing by polymerisation) are bound to the crosslinking agent. According to the invention adhesive compositions with crosslinking agent particles that have, referred to their surface, at least 0.00001 mmole x m-2 functional groups having a crosslinking action, are preferred. Typically the density of the groups having a crosslinking action is in the range from 0.1 to 1 mmole per 100m2 of specific surface of the crosslinking agent particle. The crosslinking agent particles according to the invention consequently form after the curing reaction a stellate crosslinking centre in the polymer network. If the functional groups on the crosslinking agent units are for example epoxide groups, then these may be employed with BF3 etherate as curing catalyst for crosslinking monofunctional epoxide resins. After curing, a thermoset is then formed; without the crosslinking agent particles according to the invention only a linear polymer capable of withstanding slight stress would be formed. The adhesive compositions according to the invention preferably contain filler particles that are surface- modified and are selected from the group comprising iron, iron alloys and iron-containing metal oxides. Suitable for example are filler particles that are based on iron powder, magnetite powder, superparamagnetic iron oxide or manganese-zinc-iron oxide. For example, nanoscale magnetite powder with a silicon dioxide shell may be surface-modified or functionalised with epoxide groups by reaction with 3-glycidoxypropyltrimethoxysilane. If a sol-gel process is used a reaction with an epoxysilane may at the same time also take place, which means that a reaction step can be omitted. However, another functional silane may also be used for a one-stage or two-stage surface modification. The functional groups of the silane are in this connection chosen so that they can react with the polymer system to be crosslinked. Suitable pairs of functional groups of the crosslinking agent component and of the polymer system are for example the pairs listed in DE 197 33 643 Al, page 4. For example, a thermoset based on isocyanate prepolymers is obtained if the crosslinking agent particles according to the invention are surface- modified with aminopropyltrimethoxysilane. By reacting the amino groups with the dimeric isocyanate, urea couplings are formed as crosslinking sites. In the case of acrylate resins the modification of the crosslinking agent particles is preferably carried out with silanes containing acrylate or methacrylate groups, and in the case of mercaptans is preferably carried out with epoxysilanes. Particularly preferred are adhesive compositions with filler particles that have been produced by flame pyrolysis. Such filler particles may be particles or aggregated particles with superparamagnetic iron oxide .domains having a diameter of 3 to 20 nm in a silicon dioxide matrix. The production of such particles is described for example by Zachariah et al. in Nanostructured Materials 5, 383 (1995) or Ehrman et al. in Journal of Materials Research 14, 4551 (1999). Particularly preferred are the iron oxide-silicon dioxide composite particles described in DE 10140089.6 of application date 16.08.2001. Filler particle domains are understood to be superparamagnetic regions spatially separated from one another. On account of the flame pyrolysis process these particles are largely pore-free and contain free hydroxyl groups on the surface. They exhibit superparamagnetic properties when an external magnetic field is applied. The proportion of superparamagnetic iron oxide domains of the filler particles may lie between 1 and 99.6 wt.%. Regions of superparamagnetic iron oxide domains spatially separated by the non-magnetic matrix are present in this range. The range with a proportion of superparamagnetic domains greater than 30 wt.%, particularly preferably greater than 50 wt.%, is preferred. The achievable magnetic effect of" the particles according to the invention also increases in step with the proportion of the superparamagnetic regions. In these domains the iron oxide may be present in a uniform modification or in different modifications. In addition regions of non-magnetic modifications may also be present in the particles. These may be mixed oxides of silicon dioxide and iron oxide. Iron silicalite (FeSiO4) may be mentioned by way of example. These non-magnetic constituents behave like the non-magnetic silicon dioxide matrix as regards superparamagnetism. In other words the domains remain superparamagnetic, although the saturation magnetisation drops with increasing proportion of the non- magnetic constituents. In addition iron oxide domains may also be present that on account of their size do not exhibit superparamagnetism and induce a remanence. This leads to an increase in the volume-specific saturation magnetisation. Suitably adapted composite particles can be produced depending on the field of application. A particularly preferred superparamagnetic iron oxide domain is gamma-Fe2O3 (Y-Fe2O3) , Fe3O4/ and mixtures thereof. Apart from the spatial separation of the superparamagnetic iron oxide domains, the silicon dioxide matrix also has the task of stabilising the oxidation state of the domains. Thus, for example, magnetite is stabilised as superparamagnetic iron oxide phase by a silicon dioxide matrix. According to a particular embodiment the carbon content of the filler particles may be less than 500 ppm. Particularly preferably the content is less than 100 ppm. The filler particles may furthermore have a chloride content of 50 to 1000 ppm, originating from the production of the particles. The particles are obtained by a flame pyrolysis process in which chlorine-containing precursors are reacted for example in a hydrogen/oxygen flame. The particles that are formed may contain chlorine for example in the form of oxychlorides from the reaction that has not gone to completion, as well as chlorine in the form of hydrochloric acid. If these compounds are enclosed in the particles that are formed, the chloride content of the particles cannot be reduced further even by purification steps, without the particles being destroyed. The chloride content can be reduced to values of ca. 50 ppm by purification steps. The filler particles may have different degrees of aggregation depending on the conditions of the flame pyrolysis process. Influencing parameters may include the residence time, temperature, pressure, the partial pressures of the compounds that are used, and the nature and site of the cooling step after the reaction. A broad spectrum ranging from largely spherical to largely aggregated composite particles may thus be obtained. The BET surface, determined according to DIN 66131, of the filler particles may vary over a wide range from 10 to 600 m2/g. Particularly preferably the range is between 50 and 300 m2/g. In a preferred embodiment of the composite particles the "blocking temperature", i.e. the temperature below which superparamagnetic behaviour can no longer be detected, may be no more than 150 K. This temperature may depend on, apart from the composition of the particle, also on the size of the superparamagnetic domains and their anisotropy. The composite particles of superparamagnetic iron oxide and silicon dioxide as filler particles are then reacted on the surface with for example silanes, which may additionally carry groups that can react with the adhesive. In this way the inductively excitable crosslinking agent particles are obtained. In an advantageous modification of the invention the filler particles are bound via a thermally labile group to the crosslinking agent units. Suitable thermally labile groups are in particular azo groups, carbonate groups or ethylene groups with sterically demanding substituents. When adhesive compositions with such thermally labile groups are heated a bond rupture occurs at a specific temperature, whereby for example nitrogen or carbon dioxide are formed in the examples given above, or the carbon-carbon bond of the ethylene group with sterically demanding substituents is ruptured. A filler particle to which the crosslinking agent units are bound via a thermally labile group is shown for example in Fig. 1B or Fig. 2B, in which the filler particles are present in agglomerated form. In a variant the adhesive composition, which can be heated by means of an electrical field, magnetic field, electromagnetic field, alternating electrical field, alternating magnetic field or alternating electromagnetic field, contains a polymer, a polymer mixture or a reactive resin, a thermally labile substance, a crosslinking agent component, as well as filler particles that are metallic, ferromagnetic, ferrimagnetic, superparamagnetic or paramagnetic. Such adhesive compositions are particularly suitable for the production of hardened adhesive joints that are to be re-dissociated by inductive heating. Adhesive compositions within the meaning of this variant also include in particular adhesives, paints, primers, casting compositions, sealants and laminating resins. All polymers and polymer mixtures that are suitable for the uses mentioned in the introduction may also be regarded as polymers, polymer mixtures and reactive resins within the meaning of this variant. Crosslinked polymers are also preferred for this variant, particularly preferably polymers or reactive resins from which structural or semi-structural joints can be produced. In particular epoxide resins, polyurethanes, acrylates, phenol resins, polysulfides or melamine resins are suitable. The inductively excitable fillers are present either in the form of singular nanoparticles or aggregates, or in the form of agglomerates. They are preferably found in direct contact with the thermally labile substance, so that the heating takes place selectively at the site at which bonds are to be ruptured. Particularly preferably the thermally labile substance is therefore bound to the inductively excitable fillers. Also preferred are filler particles that carry a silicon dioxide-containing coating. These have a high long-term resistance to moisture. The crosslinking agent carries functional groups that undergo crosslinking reactions with the polymer, the polymer mixture or the reactive resin, which may be thermally accomplished either inductively or also in a conventional way. Suitable groups that undergo crosslinking reactions include for example epoxide, amino, The adhesive compositions of this variant accordingly have the advantage that, after they are cured, adhesive joints are formed that can be cleanly separated by means of inductive heating, with savings in time and energy. If the filler particles are in direct contact with the thermally labile substance, then the heating is carried out selectively at the site at which the bonds of the thermally labile substance are to be ruptured. This has the advantage that the whole polymer is not destroyed, as would be the case for example if the heating were carried out with a welding torch or laser. A non-selective thermal destruction of the polymer may therefore be avoided. As thermally labile substances added to the adhesive composition, in particular those substances are suitable that have average particle sizes between 2 nm and 100 µm, preferably between 2 nm and 1 µm and particularly preferably between 2 nm and 200 nm. Such particles may be present individually or in the form of agglomerates. If adhesive joints that are obtainable by curing such adhesive compositions are heated, then bonds are ruptured or phase transformations take place in these thermally labile substances and the polymer network is destabilised, whereby a rupture of the adhesive joint is possible. In an advantageous modification the thermally labile substance is a blowing agent that forms a gas under the action of heat, the gas formation temperature being higher than the temperature at which the crosslinking of the adhesive composition starts. The dissociation of adhesive composites that have been produced from such adhesive compositions is carried out by inductive heating of the particles coupled to the blowing agent, via the decomposition temperature of the blowing agent or of the blowing agent component and the resultant thermal decomposition. The gaseous decomposition products that are formed "blast" the adhesive composite apart. Suitable blowing agents include for example substances that split off water of crystallisation (e.g. aluminium nitrate), organic carboxylic acids (e.g. oxalic acid, glutaric acid), azo compounds (e.g. azodicarbonamide, azoisobutyronitrile), or fluorinated hydrocarbons. Particularly preferred blowing agents are azodicarbonamide and sulfohydrazides, such as in particular toluene sulfohydrazide and oxygen-bis(benzosulfohydrazide). In general derivatives of azodicarbonamide are also suitable. The blowing agents may optionally be activated with zinc salts. These blowing agents have the advantage that they release a large amount of gas, are sparingly soluble in organic media, decompose at 180° to 200°C, i.e. above the temperature of use of normal bonded joints, and are not toxic. If necessary the decomposition temperature may be reduced by additional activators and thereby adjusted to the conditions under which it is intended to dissociate the adhesive joints. The poor solubility of the aforementioned blowing agents in organic media has the result that the blowing agent is not dissolved in the adhesive and consequently the intimate contact between the inductively heatable filler particles and the blowing agent in the adhesive is retained. In this way the effectiveness of the resin formulation according to the invention is further enhanced. In a further advantageous modification of the adhesive composition according to the invention collective particles are first of all formed from blowing agent and filler particles, in which the blowing agent may optionally be bound to the filler particles. Collective particles are therefore understood to denote particles that contain both the blowing agent as well as the filler particles. These collective particles are obtained by precipitation, compression, microencapsulation or binding of blowing agents and filler particles with a polymer. The size of such collective particles is limited simply by the subsequent use. Such collective particles have the advantage that inductively heatable blowing agent particles that are readily compatible with the adhesive matrix can be produced. The blowing agent cannot therefore be released by the resin system and the intimate contact between inductively heatable filler particles and the blowing agent is retained. Preferably the polymer for the formation of the collective particles is expandable polystyrene. The collective particles are accordingly polystyrene beads that contain at the same time the inductively heatable filler particles and a blowing agent that is normally used to expand polystyrene. Such polystyrene beads preferably have a size of 1 µm to 1 mm. When adhesive composites that have been produced from adhesive compositions that contain these polystyrene beads are inductively heated, this leads to an expansion of the polystyrene particles and thus to the dissociation of the adhesive composite. The adhesive composition according to the invention is preferably used for adhesives, paints, sealants, primers, matrix resins or casting resins. A process for curing the adhesive composition according to the invention to form adhesive joints consists in inductively heating the adhesive composition by means of an electrical field, magnetic field, electromagnetic field, alternating electrical field, alternating magnetic field or alternating electromagnetic field, to a temperature at which the crosslinking of the adhesive composition starts. This process has the advantage that the duration of the inductive heating is normally in the range from seconds to minutes, and is thus significantly shorter than in the conventional thermal curing processes. Accordingly it is particularly suitable for curing the adhesive compositions according to the invention on sensitive objects. Also, this process is very energy-efficient. The curing process according to the invention may in particular be carried out as described in Ortwin Hahn, Andrea Kaimann, Adhäsion - Kleben und Dichten, 10/2001, pp. 35 to 38 for adhesive compositions containing coarse particulate fillers. The addition of curing catalysts and activators, as is also described in unpublished specification DE 10127704.0, is advantageous. The adhesive composite obtained by the process according to the invention for curing the adhesive composition according to the invention contains at least one hardened adhesive layer. In particular such an adhesive composite may be an adhesive joint, a cast structural part, a sealing structural part or a polymer laminate. The cured adhesive layer may be a paint layer or a primer layer. The process according to the invention for the thermal dissociation of the adhesive composite that can be obtained by curing the adhesive composition according to the invention is carried out by inductively heating the hardened layer of the adhesive composition by means of an electrical field, magnetic field, electromagnetic field, alternating electrical field, alternating magnetic field or alternating electromagnetic field. If the adhesive composition contains the crosslinking agent particles according to the invention, then the hardened layer of the adhesive composition is heated in the process according to the invention to a temperature that lies above the ceiling temperature of the crosslinking points. If the adhesive composition contains filler particles and a thermally labile substance, then the hardened layer of the adhesive composition is heated inductively to a temperature at which the thermally labile bonds of the thermally labile substance or of the thermally labile group rupture. In the process according to the invention for the thermal dissociation of the hardened adhesive composites, the filler particles are thus inductively heated, whereby a chemical reaction is initiated in which either the thermally labile substances effect a rupture of the crosslinking points of the polymer network due to bond rupture, formation of gas and/or swelling effects, or in which, due to the inductive heating of the filler particles, a bond rupture takes place at the crosslinking points lying in the immediate vicinity of the filler particles. The dissociation of the adhesive composites according to the invention thus takes place selectively by the action of the high-frequency energy from a conventional induction coil. Due to resultant eddy currents, particle movements in the alternating field and hystoresis losses, the metallic, ferromagnetic, ferrimagnetic, superparamagnetic or paramagnetic filler particles according to the invention present in the polymer network are heated. At the same time there is also a heating of the polymer system in the immediate environment of the filler particles. The induction voltage is chosen so that the heat that is generated is sufficient to dissociate the crosslinking points in the polymer network and to destroy the latter thermally in the case where heating is combined with blowing agents. The induction frequencies are preferably between a few kilohertz and about 35 megahertz. The equipment, parameters and equipment adjustments required in each case depend on the filler that is used and its content in the polymer system. In particular, the particle size distribution, Curie temperature, permeability, electrical resistance, coefficient of thermal expansion and the specific thermal capacity are quantities on which depends the achievable temperature for a specific setting of the equipment. The temperature required for the dissociation depends on the thermal stability of the respective polymer system and blowing agent. If the filler particles that are used are chemically bound to the crosslinking sites of the polymer system, then the filler itself is a constituent of the polymer system. On account of the localised vicinity of the chemical bonds to be separated to the filler particles introduced according to the invention and heatable by induction, the separation is in this case particularly effective. The process according to the invention for dissociating adhesive composites may be used on bonded joints that consist only of the adhesive itself according to the invention, though there may also be used an adhesive primer based on the adhesive compositions according to the invention in combination with a commercially available adhesive. In this case the dissociation of the composite takes place selectively in the primer layer. The adhesive remains on one of the two bonded parts. If the adhesive composition according to the invention is a paint that is to be inductively pickled, then in particular adhesive compositions according to the invention are advantageous in which the filler particles are bound to the crosslinking agent component. This has the advantage that no chemicals, no expensive equipment and no high labour expenditure are necessary for the pickling. Furthermore the paints that can be inductively pickled are particularly suitable for sensitive substrates. As examples there may be mentioned fibre-reinforced composite plastics, in which the base polymers are damaged by the pickling chemicals, or the fibres may be exposed or damaged during the grinding. Both phenomena lead to an unallowable weakening of the sensitive structural part. The process according to the invention for the inductive pickling is suitable in particular for carbon fibre- reinforced structural parts of aircraft or glass fibre- reinforced composites in ships' carcasses and wind power blades. Without restricting its general applicability, the adhesive composition according to the invention, the process for curing the latter to form an adhesive composite and the dissociation of this adhesive composite are described in more detail hereinafter with the aid of examples of use. Example 1 - Curing and dissociation of a bonded joint with inductively excitable filler particles bound to a crosslinking agent la) Nanoscale magnetite coated with silicon dioxide 43.3 g of iron(III) chloride hexahydrate are dissolved in 370 ml of water and freed from dissolved oxygen by passing nitrogen through the solution. 15.9 g of iron(II) chloride tetrahydrate are added and a solution of 25.6 g of sodium hydroxide in 100 ml of water is added dropwise within 2 hours, with stirring, with a precision glass stirrer under a flowing stream of nitrogen. A finely particulate black precipitate of Fe3O4 is thereby formed. A solution of 22 g of Na2Si307 (annealing loss 17 wt.%) in 80 ml of hot water is then added dropwise within 30 minutes. The silicic acid is now precipitated, with further stirring, by slow dropwise addition of hydrochloric acid (14 ml of 37% hydrochloric acid made up to 50 ml with water). The precipitate is filtered and made into a slurry five times with distilled water and is in each case refiltered in order to separate the sodium chloride formed. The resulting material consists of agglomerated nanoparticles. The primary particles have a diameter of about 8 nm (determined by transmission electron microscopy) and the agglomerates have a diameter of about 400 nm (determined by light scattering). lb) Modification of the nanoscale, inductively excitable filler particles 20 g of the nanoscale magnetite produced according to Example la with a residual moisture content of 40% or a comparable material from another source is made into a slurry with acetone, made up to a total volume of 300 ml, acidified with 0.3 ml of conc, hydrochloric acid, following which 15 g of epoxycyclohexyltrimethoxysilane are added. The whole is stirred for 24 hours with a precision glass stirrer and then dried in vacuo on a rotary evaporator. The surface-modified filler carries cycloaliphatic epoxide groups on the surface and is able to act as a crosslinking agent in the adhesive system. lc) Incorporation of the surface-modified filler into an adhesive 10 g of 3,4-epoxycyclohexylmethyl-3',4'-epoxycyclohexane- carboxylate, 10 g of cyclohexene oxide, 0.2 g of (tolylcumyl) iodonium tetrakis(pentafluorophenyl) borate and 0.2 g of ascorbic acid-6-hexadecanoate are stirred until a homogeneous mixture is formed (base mixture according to unpublished specification DE 10127704.0). 4 g of the surface-modified filler according to b) are incorporated using a dissolver. After stirring for 15 minutes a homogeneous thixotropic mass has formed, which is used hereinafter as adhesive. 1d) Bonding with inductive curing and re-dissociation of the bonded joint 25 mm- wide and 4 mm- thick parts to be joined consisting of glass fibre-reinforced polyester are bonded with the adhesive produced according to c). For this, a part to be joined is coated in the joining region with a 0.2 mm- thick adhesive layer, the second part is placed thereon, and both parts are fixed under a light pressure (ca. 0.02 N/mm2) . The subsequent curing of the adhesive is carried out by excitation with an M230 semiconductor generator from STS. The excitation frequency of this generator is 300 kHz. A coil with three windings and an internal diameter of 3 cm is used for the inductive excitation of the adhesive in the bonded joint. The adhesive surface is aligned in the middle of the coil, perpendicular to the coil axis. The adhesive is cured at an output of 1000 W and an action time of 5 minutes, a firm joint thereby being obtained. This is then dissociated within 60 secs by increasing the generator output to 3000 W. In a comparison example without inductively excitable nanoscale filler"particles, it is not possible to cure the adhesive even at an output of 3 000 W and an action time of 10 minutes. Example 2 - Bonded joint that can be dissociated by an inductively excitable blowing agent 2a) Formulation from magnetite powder and blowing agent 20 g of the material produced according to la) (residual moisture of the filter cake 40%) or a nanoscale magnetite powder obtained from another source is suspended in 100 ml of ethanol and 20 g of oxy-bis(benzosulfohydrazide) are added as blowing agent. The mixture is heated for 4 hours at 70°C with stirring, and the solvent is then removed on a rotary evaporator. The dry formulation is ground in a ball mill for 5 minutes and then screened. The fraction with a grain size of nominally less than 63 µm is used for the further tests. 2b) Incorporation of the formulation from Example 2a) in an adhesive 8 g of 3,4-epoxycyclohexylmethyl-3',4'-epoxycyclohexane- carboxylate, 2 g of poly(tetrahydrofuran) of Mn=250, 0.1 g of (tolylcumyl) iodonium tetrakis (pentafluorophenyl) borate and 0.04 g of ascorbic acid-6-hexadecanoate are stirred until the components have dissolved in one another (base mixture according to unpublished specification DE 10127704.0). 2 g of the formulation are then stirred in, whereupon the material assumes a doughy consistency. A part of the sample cures within 3 0 minutes at 90°C to form a tack-free polymer. 2c) Bonding and re-dissociation of a plastics joint 25 mm- wide and 3 mm- thick polypropylene parts to be joined are pretreated by fluorination according to the prior art, coated with a ca. 0.2 mm- thick layer of the inductively excitable formulation, following which a second part is placed thereon and is cured under a light pressure (ca. 0.02 N/mm2) for 3 0 minutes in an oven at 90°C. The subsequent separation of the joint is carried out by excitation with an M230 semiconductor generator from STS. The excitation frequency of this generator is 300 kHz. A coil with three windings and an internal diameter of 3 cm is used for the inductive excitation of the adhesive in the bond joint. The adhesive surface is aligned in the middle of the coil, perpendicular to the coil axis. With an output of 1500 W and an action time of 25 secs, the blowing agent has decomposed and thereby dissociated the bonded joint. In a comparison example without the nanoscale magnetite powder, the bonded joint cannot be dissoicated even under the action of an output of 3 000 W for 2 minutes. The analytical data of the iron oxide-silicon dioxide composite particles used in Examples 3 to 6 are shown in Table 1. The production of these particles is described in DE 10140089.6. Example 3 - Dissociation of a glass bond based on an adhesive with inductively excitable blowing agent 3a) Formulation from composite particles produced by flame pyrolysis and a binder 25 g of nanoscale composite particles produced by flame pyrolysis and consisting of silicon dioxide and iron oxide having the properties shown in Table 1 are suspended in 100 ml of ethanol and 20 g of oxy-bis(benzosulfohydrazide) are added as blowing agent. The mixture is heated for 5 hours at 60°C with stirring, and the solvent is then removed on a rotary evaporator. The dry formulation is ground in a ball mill for 3 minutes and then screened. The fraction with a grain size of nominally less than 63 µm is used for the further tests. 3b) Incorporation of the formulation from Example 3a) in an adhesive, and adhesive tests 3 00 g of the moisture-hardening one-component polyurethane adhesive Dinitrol PUR 501 FC (Dinol GmbH) are modified in a Planimax (Molteni) mixer provided with kneading hooks, with 10 g of the formulation produced according to Example 3a and consisting of blowing agent and inductively excitable nanofiller. The mixture is kneaded for 15 minutes at setting 1 (150 rpm) in a dry atmosphere. A thick layer bond between a sand-blasted and degreased aluminium sheet and a 3 mm- thick float glass panel is prepared using the thereby modified adhesive. The overlap length is 25 mm and the adhesive layer thickness is 3 mm. After a curing time of 1 week at 25°C and 50% relative atmospheric humidity the joint is re-separated by inductive excitation. The separation of the joint is carried out by excitation with an M23 0 semiconductor generator from STS. The excitation frequency of this generator is 300 kHz. A coil with three windings and an internal diameter of 3 cm is used for the inductive excitation of the adhesive in the bonded joint. The adhesive surface is aligned in the middle of the coil, perpendicular to the coil axis. At an output of 3000 W and an action time of 2 minutes the adhesive is destroyed by the expansion of the blowing agent. The two joined parts can easily be separated from one another. Example 4 - Dissociable bonded joint based on an inductively dissociable adhesive primer 5 g of the formulation prepared according to Example 3a and consisting of blowing agent and inductively excitable nanofiller are stirred into 200 g of the Sika-Primer 206G+P (Sika AG) adhesive primer. The primer is applied to a sand-blasted and degreased aluminium sheet so as to cover the latter. After an aeration time of 1 hour the sheet pretreated in this way is bonded with a 3 mm- thick layer of beech plywood. Sikaflex 254 (Sika AG) is applied as adhesive in a thickness of 3 mm, and the overlap length is 25 mm. The adhesive hardens within 1 week at a relative atmospheric humidity of 50% and at 25°C. The joint is then re-separated by inductive excitation. The excitation of the adhesive for the separation is carried out with an M230 semiconductor generator from STS. The excitation frequency of this generator is 300 kHz. A coil with three windings and an internal diameter of 3 cm is used for the inductive excitation of the adhesive in the bonded joint. The adhesive surface is aligned in the middle of the coil, perpendicular to the coil axis. At an output of 3 000 W and an action time of 2 minutes the adhesive primer applied to the aluminium side is destroyed by the expansion of the blowing agent. The parts of the joint can easily be separated from one another, the adhesive remaining selectively on the plywood. Example 5 - Curing an elastic adhesive and testing the adhesive properties The elastic adhesive Elastosol M83 (Tivoli, Hamburg) is a one-component, heat-curing metal adhesive based on polybutadiene. On the basis of a comparison of the curing in a conventional oven with the inductive curing according to the invention, it will be shown that equivalent bonding results are achieved with both types of curing. In this connection the inductive curing occurs more rapidly. 25 g of the iron oxide-silicon dioxide composite particles according to Table 1 are incorporated in 250 g of the adhesive Elastosol M83 using a Planimax mixer (Molteni) equipped with kneading hooks. Kneading is first of all carried out for 5 minutes at 150 revolutions per minute and then for a further 30 minutes at 450 rpm (setting 3). The mixture is then kneaded for a further 5 minutes in vacuo to degass it (setting 3). The material according to the invention that is thus obtained is used for the adhesive tests. In order to check the adhesive properties, tensile/shear samples are produced on the basis of DIN EN 1465, one part to be joined consisting of 1.15 mm- thick rolled aluminium sheet material (AlMgo.4Si12) and another part to be joined consisting of 4 mm- thick, glass fibre-reinforced polypropylene. The aluminium is ground and degreased with butanone. The polypropylene is pretreated in a low- pressure plasma with air as working gas. Adhesive samples are first of all prepared with the modified adhesive according to the invention and inductively hardened. The curing of the adhesive is carried out by excitation with an M23 0 semiconductor generator from STS. A water-cooled flat coil with three windings and a diameter of 8 cm is used for the inductive excitation of the adhesive in the bonded joint. The coil is placed on the joined part of polypropylene and the adhesive is cured at an output of 1000 W and an action time of 10 minutes The samples have a tensile-shear strength of 10.4 ± 0.6 MPa, with a cohesive fracture of the adhesive. For purposes of comparison, tensile/shear samples are prepared with the unmodified adhesive. In this case the adhesive is cured in a conventional manner according to the manufacturer's instructions. The curing is carried out over 3 0 minutes at 180°C in an oven. The tensile-shear strength of these samples is 10.1 ± 0.4 MPa. Example 6 - Modification of a melt adhesive for the selective dissociation of bonded joints The melt adhesive B40166 (Heinrich Büuhnen GmbH)is modified with 7 wt.% of iron oxide-silicon dioxide composite particles according to Table 1 in a Brabender double-screw extruder at a screw speed of 60 rpm and a screw temperature of 22 0°C in all heating zones. The melt adhesive is granulated and applied with an HB 500 application device to 5 mm- thick beech plywood. A second piece of beech plywood is immediately pressed onto the melt adhesive. The joint is firm within 1 minute. The dissociation of the bonded joint is carried out inductively with the M230 semiconductor generator from STS and a water-cooled flat coil with three windings and a diameter of 8 cm. The coil is placed on the plywood and an output of 3000 W is adjusted at the semiconductor generator. After an action time of 60 seconds the two plywood plates can be taken apart and, after renewed inductive heating, can be rebonded to one another. WE CLAIM: Adhesive composition for the production of thermosets, the composition being able to be heated by means of an electrical field, magnetic field, electromagnetic field, alternating electrical field, alternating magnetic field or alternating electromagnetic field and containing a polymer, a polymer mixture or a reaction resin, and crosslinking agent particles, wherein the crosslinking agent particles comprise filler particles that are ferromagnetic, ferrimagnetic, superparamagnetic or paramagnetic and crosslinking agent units chemically bound to these filler particles. 2. Adhesive composition as claimed in claim 1, wherein the content of crosslinking agent particles is 0.1 wt. % to 80 wt.X, preferably 0.5 wt.X to 40 wt.% and particularly preferably 1 wt. % to 30 wt. X. 3. Adhesive composition as claimed in claim 1 or 2, wherein the crosslinking agent particles have average primary particle sizes between 2 nm and 1000 nm, preferably between 2 nm and 500 nm and particularly preferably between 2 nm and 100 nm. 4. Adhesive composition as claimed in claims 1 to 3, wherein the crosslinking agent particles have, referred to their surface, -2 at least 0.00001 mmole x m of functional groups with a crosslinking action. 5. Adhesive composition as claimed in claims 1 to 4, wherein the filler particles are surface-modified. 6. Adhesive composition as claimed in claims i to 5, wherein the filler particles are selected from the group comprising iron, iron alloys and iron-containing metal oxides. 7. Adhesive composition as claimed in claim 9, wherein the filler particles have a core-shell structure and are produced by sol-gel processes or from the reaction of nanoscale iron oxide with sodium silicate. 3. Adhesive composition as claimed in claim 5» wherein the filler particles ,are superparamagnetic iron oxide-silicon dioxide composite particles produced by flame pyrolysis. 9. Adhesive composition as claimed in claims 1 to 8, wherein the crosslinking agent units are bound via a thermally labile group to the filler particles. 10. Adhesive composition as claimed in claim 9 wherein the thermally labile group is an azo group, a carbonate group or an ethylene group with sterically demanding substituents. 11. Adhesive composition for the production of thermosets as claimed in claims 1 to 8 wherein it additionally contains a thermally labile substance. 12. Adhesive composition as claimed in claim 11 wherein the thermally labile substance has average particle sizes between 2 nm and 100 µm preferably between 2 nm and 1 µm and particularly preferably between 2 nm and 200 nm. 13. Adhesive composition as claimed in claim 11 or 12, wherein the thermally labile substance is a blowing agent that forms gas under the action of heat, in which the gas formation temperature is higher than the temperature at which the crosslinking of the adhesive composition starts. 14. Adhesive composition as claimed in claim 13, wherein the blowing agent is selected from the group comprising azodicarbonamide and sulfohydrazides, in particular toluene sulfohydrazide and oxygen-bis (benzosulfohydrazide>. 15. Adhesive composition as claimed in claim 13 or 14 wherein collective particles are included that contain the blowing agent and the filler particles and are obtainable by precipitation, compression, microencapsulation or bonding of blowing agent and filler particles with a polymer. 16. Adhesive composition as claimed in claim 15, wherein the polymer for the formation of the collective particle, is expandable polystyrene. 17. Process for the curing of an adhesive composition as claimed in claims 1 to 16, wherein the adhesive composition is inductively heated by means of an electrical field, magnetic field, electromagnetic field, alternating electrical field, alternating magnetic field or alternating electromagnetic field to a temperature at which the crosslinking of the adhesive composition starts. 18. Adhesive composite that comprises at least one adhesive layer that is obtainable by curing the adhesive composition as claimed in one or more of claims 1 to 16. 19. Adhesive composite as claimed in claim 18 wherein the at least one adhesive layer is a paint layer or primer layer. 20. Adhesive composite as claimed in claim 18 or 19 that is a bonded joint, a cast structural part, a sealed structural part or a polymer laminate. 21. Process for the thermal dissociation of an adhesive composite that can be obtained by curing the adhesive composition as claimed in claims 1 to 8, wherein the hardened layer of the adhesive composition is heated by means of an electrical field, magnetic field, electromagnetic fields alternating electrical field, alternating magnetic field or alternating electromagnetic field to a temperature that lies above the ceiling temperature of the crosslinking points. 22. Process for the thermal dissociation of an adhesive composite that can be obtained by curing the adhesive composition as claimed in claims 9 to 16, wherein the hardened layer of the adhesive composition is heated by means of an electrical field, magnetic field, electromagnetic field, alternating electrical field, alternatic magnetic field or alternating electrommagnetic field to a temperature at which the thermally labile bonds of a thermally labile substance and/or thermally labile group rupture. Adhesive composition for the production of thermosests, the composition being able to be heated by means of an electrical field, magnetic field, electromagnetic field, alternating electrical field, alternating magnetic field or alternating electromagnetic field and containing a polymer, a polymer mixture or a reaction resin, and crosslinking agent particles, wherein the crosslinking agent particles comprise filler particles that are ferromagnetic, ferrimagnetic, superparamagnetic or paramagnetic and crosslinking agent units chemically bound to these filler particles.

Full Text

Description
Technical Field
The present invention relates to an adhesive composition which contains
inductively heatable filler particles, and to its use and a process for its
curing. The invention also relates to an adhesive composite that contains a
hardened layer of the adhesive composition, a process for the thermal
dissociation of the hardened adhesive composition, and the use of this
process.
Prior Art
Adhesive bonds, i.e. in particular bonded joints, coatings, laminates or cast
structural parts are designed so that they can be produced under mild
conditions, are resistant for as long as possible and have the highest possible
strengths. High strengths mean that, in the case of a repair or recycling, a
dissociation of the adhesive bond can be carried out only under extreme
conditions, such as for example the action of strong forces or high
temperatures. Bonded joints based on hard adhesives are generally
dissociable, but are not suitable for transmitting the high forces necessary for
structural bonded joints. The dissociation of high-strength bonded joints is
generally accomplished by the use of mechanical energy or chemical agents.
The latter have the disadvantage that they cause a high environmental
pollution and also that the penetration of the agents into the
gluelines of structural bonded joints that are stable over
the long term takes far too long.
DE 43 28 108 A describes the dissociation of floor
coverings by means of microwave energy. For this purpose a
contact adhesive is used that is electrically conducting
and is filled with copper powder or aluminium powder.
These fillers have the disadvantage that the particles have
sizes of a few micrometres and larger. This leads to a
non-uniform heating of the contact adhesive.
DE 199 61 940 Al describes adhesives for dissociable bonded
joints that contain thermally activatable substances that
release gaseous compounds when they decompose, which then
destroy the bonded joints. This process has the
disadvantage that in order to separate the composite, the
whole structural part or the joined parts and the adhesive
have to be heated. This is associated with a high energy
expenditure. Furthermore it is not possible to achieve a
locally restricted separation of the structural part or of
the joined part.
DE 199 51 599 Al and DE 199 24 138 Al describe adhesives
for dissociable bonded joints and bonded joints produced
therewith, that contain externally excitable nanofillers.
The dissociation of the bonded joints is achieved by
introducing the joints into an alternating electrical,
magnetic or electromagnetic field, whereby the nanofillers
and the surrounding adhesive are heated. This process has
the disadvantage however that it leads to the heating of
the whole adhesive, also at places at which no heating is
necessary or desirable, since the excitable nanofillers are
also contained in places in the adhesive or primer where
heating is not necessary in order to achieve the desired
dissociation of the bonded joint. Furthermore high
temperatures are required to separate high-strength bonded
joints since chemical bonds have to be broken in order to
break down the composite. The described processes
furthermore have the disadvantage that a non-specific
thermal decomposition of the adhesive and/or primer occurs
when separating high-strength bonded joints. Such
processes are therefore unsuitable in particular for
thermosets.
The production of resistant, high-strength adhesive Joints
is normally carried out thermally or photochemically. The
conventional processes for producing adhesive bonded joints
have the disadvantage however that the whole structural
part has to be heated in order to cure the adhesive. As a
result the process is enerqy intensive and time-consuming
WO 99/03306 and 0. Hahn, A. Kaimann in Adhasion - Kleben
und Dichten, 10/2001, pp. 35-38 describe a process for the
inductive curing of adhesive joints. In this case
adhesives that contain inductively activatable fillers are
introduced into an electromagnetic field, whereby the
inductively activatable fillers are heated and the
hardening of the adhesive surrounding the fillers can take
place. These processes have the disadvantage however that
the inductively activatable substances are not uniformly
distributed over the adhesive and accordingly there is an
inhomogeneous heating of the adhesive. As a result, the
strength of such adhesive joints is limited. The processes
furthermore have the disadvantage that a demixing
(separation) may occur in the adhesive during the inductive
heating process and the distribution of the thermally
activatable substances in the adhesive becomes even more irregular.
Outline of the Invention
The object of the present invention is to overcome the disadvantages of the
prior art and to provide an adhesive composition that can be hardened under
mild conditions to form a resistant, high-strength adhesive joint. A further
object of the present invention is to provide a process for dissociating such
adhesive joints without the long-term resistance of the adhesive joint
inevitably suffering thereby.
These objects are achieved by the adhesive composition the process for their
curing the adhesive composite and the process for the thermal dissociation of
the hardened adhesive composition. Uses of the adhesive composition and of
the process for dissociating the hardened adhesive composition are
mentioned in details in the specification. The subclaims disclose
advantageous modifications.
It was found that adhesive compositions that contain a polymer, a polymer
mixture or a reaction resin, as well as particles of crosslinking agent, can be
heated by means of an electrical field, magnetic field, electromagnetic field,
alternating electrical field, alternating magnetic field or alternating
electromagnetic field. The particles of crosslinking agent consist in this
connection of filler particles that are metallic, ferromagnetic, ferromagnetic,
superparamagnetic or paramagnetic, as well as crosslinking
agent units that are chemically bound to the filler
particles.
A chemical reaction between the crosslinking agent unit anc
the polymer or the polymer mixture is triggered by
inductive heating of the particles of crosslinking agent,
whereby a polymer network is formed.
Adhesive compositions within the meaning of the present
invention include in particular adhesives, paints, primers,
casting compositions, sealants and laminating resins. In
particular bonded joints, painted structural parts or
structural parts provided with a primer, cast structural
parts, sealed structural parts or polymer laminates are
thereby formed by curing these adhesive compositions. As
polymers, polymer mixtures and reaction resins within the
meaning of the present invention there may be used all
polymers, polymer mixtures and reaction resins that are
considered suitable for the aforementioned applications.
Preferred are crosslinked polymers, particularly preferably
polymers or reaction resins from which structural or
semi-structural joints can be produced. In particular
epoxide resins, polyurethanes, acrylates, phenol resins,
polysulfides or melamine resins are suitable.
According to the invention the filler particles are
chemically bound to the crosslinking agent component. This
chemical bonding may be of an ionic, co-ordinative or
covalent nature. Van-der-Waals interactions for example
are also included under this heading.
In order to produce the chemical bonds according to the
invention it is advantageous if the surfaces of the filler
particles are surface-modified, i.e. if they carry
functional groups on their surface that can readily react
with functional groups of the crosslinking agent unit. The
crosslinking agent unit for its part carries at least one
functional group that on heating can undergo crosslinking
reactions with the polymer, the polymer mixture or the
reactive resin. The heating may in this connection be
accomplished either inductively or also in a conventional
way. Suitable functional groups that undergo crosslinking
reactions include for example epoxide, amino, thiol,
alcohol, acrylate, methacrylate or vinyl groups.
Chemical groups bound to the crosslinking agent unit that
can react with the filler surface are in particular
alkoxysilanes, alkoxy titanates and alkoxy zirconates.
These lead to a bonding to the normally metallic or oxidic
surface of the filler particles.
Filler particles consisting of inductively excitable
materials in the interior of the particles as well as of a
particle surface predominantly of silicon dioxide are
particularly preferred. They may be used in spherical or
aggregated form. The predominantly spherical filler
particles with a core-shell structure (see Fig. 1A,
Fig. 2A) can be obtained for example via sol-gel processes
or from the reaction of nanoscale iron oxide with sodium
silicate; the aggregated filler particles with a silicon
dioxide surface (Fig. 1B, Fig. 2B) are preferably obtained
by means of gas phase synthesis. These particles are
hereinafter termed composite particles. These composite
particles consist of aggregates that exhibit the
characteristic "sinter neck"; multiple inclusions or domains
of the inductively excitable material are found distributed
in the interior of the aggregates, while on the surface the
composite particles consist largely of silicon dioxide.
Particles with silicon dioxide on the surface have a high
long-term resistance, with respect to moisture, of the bond
between the crosslinking agent unit and the filler particle
surface and react rapidly with the aforementioned chemical
groups. Furthermore, the silicon dioxide layer protects
the inductively excitable components against chemical
attack by constituents of the formulation.
The crosslinking agent particles according to the invention
can be used for example as crosslinking agents for epoxide
resins. This epoxide resin may for example be a
bisphenol A diglycidyl ether hardened with a diamine. By
using such crosslinking agent particles a thermoset is
obtained that can be subjected to high chemical and thermal
stress. An individual crosslinking agent particle with
epoxide groups is shown diagrammatically by way of example
in Fig. 1A. The filler particles may also be present in
the form of agglomerates, as shown in Fig. 2A. Fig. 2A
shows diagrammatically a section from an agglomerate of
iron oxide particles in a silicon dioxide matrix.
The adhesive compositions according to the invention have
the advantage that the distribution of the filler particles
is such that they are located only at those places where
their action is necessary, namely in the crosslinking agent
particles. Compared to the previously known adhesive
compositions, the filler particles are in this case in
direct (i.e. molecular or almost molecular) contact at
those places at which their effect is to be manifested. In
this way a non-specific heating of the whole polymer is
avoided during inductive heating. The adhesive
compositions according to the invention may therefore be
inductively hardened under mild conditions.
In addition the adhesive compositions according to the
invention have the advantage that adhesive joints produced
therefrom can also be inductively and cleanly re-separated,
with savings in time and energy, without having to add
substances that facilitate a separation. Here too the
heating takes place selectively on a molecular level at the
site at which the bonds are to be broken. This has the
advantage that the whole polymer is not destroyed, as would
be the case for example if it were heated with a welding
torch or laser. A non-selective thermal decomposition of
the polymer can thereby be avoided.
Naturally, a lower induction output, i.e. for example a
lower output of the high-frequency generator, is necessary
for the crosslinking or curing than for the separation of
the adhesive joint.
According to the invention, in particular adhesive
compositions are suitable that have a content of
crosslinking agent particles of 0.1 to 80%, preferably 0.5
to 40% and particularly preferably 1% to 30%. By
increasing the content of crosslinking agent particles or
crosslinking agent units, a higher degree of crosslinking
and thus a higher strength is achieved-.
Advantageously the crosslinking agent particles have an
average primary particle size, i.e. an average primary
particles diameter, of less than 1000 nm, preferably less
than 500 nm and particularly preferably between 2 nm and
100 nm. A uniform crosslinking of the adhesive composition
according to the invention is achieved in this way.
Furthermore, such small particle sizes are most suitable
from the point of view of energy economy.
The filler particles according to the invention may be
present in an agglomerated state if the dispersion quality
is insufficient. The crosslinking agent particles
preferably comprise at least three functional groups having
a crosslinking action, a thermoset thereby being formed. A
thermoset is then generally obtained if three chemical
groups (polymer systems curing by polycondensation or by
polyaddition) or possibly even two chemical groups (polymer
systems curing by polymerisation) are bound to the
crosslinking agent. According to the invention adhesive
compositions with crosslinking agent particles that have,
referred to their surface, at least 0.00001 mmole x m-2
functional groups having a crosslinking action, are
preferred. Typically the density of the groups having a
crosslinking action is in the range from 0.1 to 1 mmole per
100m2 of specific surface of the crosslinking agent
particle. The crosslinking agent particles according to
the invention consequently form after the curing reaction a
stellate crosslinking centre in the polymer network. If
the functional groups on the crosslinking agent units are
for example epoxide groups, then these may be employed with
BF3 etherate as curing catalyst for crosslinking
monofunctional epoxide resins. After curing, a thermoset
is then formed; without the crosslinking agent particles
according to the invention only a linear polymer capable of
withstanding slight stress would be formed.
The adhesive compositions according to the invention
preferably contain filler particles that are surface-
modified and are selected from the group comprising iron,
iron alloys and iron-containing metal oxides. Suitable for
example are filler particles that are based on iron powder,
magnetite powder, superparamagnetic iron oxide or
manganese-zinc-iron oxide. For example, nanoscale
magnetite powder with a silicon dioxide shell may be
surface-modified or functionalised with epoxide groups by
reaction with 3-glycidoxypropyltrimethoxysilane. If a
sol-gel process is used a reaction with an epoxysilane may
at the same time also take place, which means that a
reaction step can be omitted. However, another functional
silane may also be used for a one-stage or two-stage
surface modification. The functional groups of the silane
are in this connection chosen so that they can react with
the polymer system to be crosslinked. Suitable pairs of
functional groups of the crosslinking agent component and
of the polymer system are for example the pairs listed in
DE 197 33 643 Al, page 4. For example, a thermoset based
on isocyanate prepolymers is obtained if the crosslinking
agent particles according to the invention are surface-
modified with aminopropyltrimethoxysilane. By reacting the
amino groups with the dimeric isocyanate, urea couplings
are formed as crosslinking sites. In the case of acrylate
resins the modification of the crosslinking agent particles
is preferably carried out with silanes containing acrylate
or methacrylate groups, and in the case of mercaptans is
preferably carried out with epoxysilanes.
Particularly preferred are adhesive compositions with
filler particles that have been produced by flame
pyrolysis.
Such filler particles may be particles or aggregated
particles with superparamagnetic iron oxide .domains having
a diameter of 3 to 20 nm in a silicon dioxide matrix. The
production of such particles is described for example by
Zachariah et al. in Nanostructured Materials 5, 383 (1995)
or Ehrman et al. in Journal of Materials Research 14, 4551
(1999).
Particularly preferred are the iron oxide-silicon dioxide
composite particles described in DE 10140089.6 of
application date 16.08.2001.
Filler particle domains are understood to be
superparamagnetic regions spatially separated from one
another. On account of the flame pyrolysis process these
particles are largely pore-free and contain free hydroxyl
groups on the surface. They exhibit superparamagnetic
properties when an external magnetic field is applied. The
proportion of superparamagnetic iron oxide domains of the
filler particles may lie between 1 and 99.6 wt.%. Regions
of superparamagnetic iron oxide domains spatially separated
by the non-magnetic matrix are present in this range. The
range with a proportion of superparamagnetic domains
greater than 30 wt.%, particularly preferably greater than
50 wt.%, is preferred. The achievable magnetic effect of"
the particles according to the invention also increases in
step with the proportion of the superparamagnetic regions.
In these domains the iron oxide may be present in a uniform
modification or in different modifications.
In addition regions of non-magnetic modifications may also
be present in the particles. These may be mixed oxides of
silicon dioxide and iron oxide. Iron silicalite (FeSiO4)
may be mentioned by way of example. These non-magnetic
constituents behave like the non-magnetic silicon dioxide
matrix as regards superparamagnetism. In other words the
domains remain superparamagnetic, although the saturation
magnetisation drops with increasing proportion of the non-
magnetic constituents.
In addition iron oxide domains may also be present that on
account of their size do not exhibit superparamagnetism and
induce a remanence. This leads to an increase in the
volume-specific saturation magnetisation. Suitably adapted
composite particles can be produced depending on the field
of application.
A particularly preferred superparamagnetic iron oxide
domain is gamma-Fe2O3 (Y-Fe2O3) , Fe3O4/ and mixtures thereof.
Apart from the spatial separation of the superparamagnetic
iron oxide domains, the silicon dioxide matrix also has the
task of stabilising the oxidation state of the domains.
Thus, for example, magnetite is stabilised as
superparamagnetic iron oxide phase by a silicon dioxide
matrix.
According to a particular embodiment the carbon content of
the filler particles may be less than 500 ppm.
Particularly preferably the content is less than 100 ppm.
The filler particles may furthermore have a chloride
content of 50 to 1000 ppm, originating from the production
of the particles. The particles are obtained by a flame
pyrolysis process in which chlorine-containing precursors
are reacted for example in a hydrogen/oxygen flame. The
particles that are formed may contain chlorine for example
in the form of oxychlorides from the reaction that has not
gone to completion, as well as chlorine in the form of
hydrochloric acid. If these compounds are enclosed in the
particles that are formed, the chloride content of the
particles cannot be reduced further even by purification
steps, without the particles being destroyed. The chloride
content can be reduced to values of ca. 50 ppm by
purification steps.
The filler particles may have different degrees of
aggregation depending on the conditions of the flame
pyrolysis process. Influencing parameters may include the
residence time, temperature, pressure, the partial
pressures of the compounds that are used, and the nature
and site of the cooling step after the reaction. A broad
spectrum ranging from largely spherical to largely
aggregated composite particles may thus be obtained.
The BET surface, determined according to DIN 66131, of the
filler particles may vary over a wide range from 10 to
600 m2/g. Particularly preferably the range is between 50
and 300 m2/g.
In a preferred embodiment of the composite particles the
"blocking temperature", i.e. the temperature below which
superparamagnetic behaviour can no longer be detected, may
be no more than 150 K. This temperature may depend on,
apart from the composition of the particle, also on the
size of the superparamagnetic domains and their anisotropy.
The composite particles of superparamagnetic iron oxide and
silicon dioxide as filler particles are then reacted on the
surface with for example silanes, which may additionally
carry groups that can react with the adhesive. In this way
the inductively excitable crosslinking agent particles are
obtained.
In an advantageous modification of the invention the filler
particles are bound via a thermally labile group to the
crosslinking agent units. Suitable thermally labile groups
are in particular azo groups, carbonate groups or ethylene
groups with sterically demanding substituents. When
adhesive compositions with such thermally labile groups are
heated a bond rupture occurs at a specific temperature,
whereby for example nitrogen or carbon dioxide are formed
in the examples given above, or the carbon-carbon bond of
the ethylene group with sterically demanding substituents
is ruptured. A filler particle to which the crosslinking
agent units are bound via a thermally labile group is shown
for example in Fig. 1B or Fig. 2B, in which the filler
particles are present in agglomerated form.
In a variant the adhesive composition, which can be heated
by means of an electrical field, magnetic field,
electromagnetic field, alternating electrical field,
alternating magnetic field or alternating electromagnetic
field, contains a polymer, a polymer mixture or a reactive
resin, a thermally labile substance, a crosslinking agent
component, as well as filler particles that are metallic,
ferromagnetic, ferrimagnetic, superparamagnetic or
paramagnetic.
Such adhesive compositions are particularly suitable for
the production of hardened adhesive joints that are to be
re-dissociated by inductive heating.
Adhesive compositions within the meaning of this variant
also include in particular adhesives, paints, primers,
casting compositions, sealants and laminating resins. All
polymers and polymer mixtures that are suitable for the
uses mentioned in the introduction may also be regarded as
polymers, polymer mixtures and reactive resins within the
meaning of this variant. Crosslinked polymers are also
preferred for this variant, particularly preferably
polymers or reactive resins from which structural or
semi-structural joints can be produced. In particular
epoxide resins, polyurethanes, acrylates, phenol resins,
polysulfides or melamine resins are suitable.
The inductively excitable fillers are present either in the
form of singular nanoparticles or aggregates, or in the
form of agglomerates. They are preferably found in direct
contact with the thermally labile substance, so that the
heating takes place selectively at the site at which bonds
are to be ruptured. Particularly preferably the thermally
labile substance is therefore bound to the inductively
excitable fillers. Also preferred are filler particles
that carry a silicon dioxide-containing coating. These
have a high long-term resistance to moisture.
The crosslinking agent carries functional groups that
undergo crosslinking reactions with the polymer, the
polymer mixture or the reactive resin, which may be
thermally accomplished either inductively or also in a
conventional way. Suitable groups that undergo
crosslinking reactions include for example epoxide, amino,
The adhesive compositions of this variant accordingly have
the advantage that, after they are cured, adhesive joints
are formed that can be cleanly separated by means of
inductive heating, with savings in time and energy. If the
filler particles are in direct contact with the thermally
labile substance, then the heating is carried out
selectively at the site at which the bonds of the thermally
labile substance are to be ruptured. This has the
advantage that the whole polymer is not destroyed, as would
be the case for example if the heating were carried out
with a welding torch or laser. A non-selective thermal
destruction of the polymer may therefore be avoided.
As thermally labile substances added to the adhesive
composition, in particular those substances are suitable
that have average particle sizes between 2 nm and 100 µm,
preferably between 2 nm and 1 µm and particularly
preferably between 2 nm and 200 nm.
Such particles may be present individually or in the form
of agglomerates. If adhesive joints that are obtainable by
curing such adhesive compositions are heated, then bonds
are ruptured or phase transformations take place in these
thermally labile substances and the polymer network is
destabilised, whereby a rupture of the adhesive joint is
possible.
In an advantageous modification the thermally labile
substance is a blowing agent that forms a gas under the
action of heat, the gas formation temperature being higher
than the temperature at which the crosslinking of the
adhesive composition starts.
The dissociation of adhesive composites that have been
produced from such adhesive compositions is carried out by
inductive heating of the particles coupled to the blowing
agent, via the decomposition temperature of the blowing
agent or of the blowing agent component and the resultant
thermal decomposition. The gaseous decomposition products
that are formed "blast" the adhesive composite apart.
Suitable blowing agents include for example substances that
split off water of crystallisation (e.g. aluminium
nitrate), organic carboxylic acids (e.g. oxalic acid,
glutaric acid), azo compounds (e.g. azodicarbonamide,
azoisobutyronitrile), or fluorinated hydrocarbons.
Particularly preferred blowing agents are azodicarbonamide
and sulfohydrazides, such as in particular toluene
sulfohydrazide and oxygen-bis(benzosulfohydrazide). In
general derivatives of azodicarbonamide are also suitable.
The blowing agents may optionally be activated with zinc
salts. These blowing agents have the advantage that they
release a large amount of gas, are sparingly soluble in
organic media, decompose at 180° to 200°C, i.e. above the
temperature of use of normal bonded joints, and are not
toxic. If necessary the decomposition temperature may be
reduced by additional activators and thereby adjusted to
the conditions under which it is intended to dissociate the
adhesive joints. The poor solubility of the aforementioned
blowing agents in organic media has the result that the
blowing agent is not dissolved in the adhesive and
consequently the intimate contact between the inductively
heatable filler particles and the blowing agent in the
adhesive is retained. In this way the effectiveness of the
resin formulation according to the invention is further
enhanced.
In a further advantageous modification of the adhesive
composition according to the invention collective particles
are first of all formed from blowing agent and filler
particles, in which the blowing agent may optionally be
bound to the filler particles. Collective particles are
therefore understood to denote particles that contain both
the blowing agent as well as the filler particles.
These collective particles are obtained by precipitation,
compression, microencapsulation or binding of blowing
agents and filler particles with a polymer. The size of
such collective particles is limited simply by the
subsequent use. Such collective particles have the
advantage that inductively heatable blowing agent particles
that are readily compatible with the adhesive matrix can be
produced. The blowing agent cannot therefore be released
by the resin system and the intimate contact between
inductively heatable filler particles and the blowing agent
is retained.
Preferably the polymer for the formation of the collective
particles is expandable polystyrene. The collective
particles are accordingly polystyrene beads that contain at
the same time the inductively heatable filler particles and
a blowing agent that is normally used to expand
polystyrene. Such polystyrene beads preferably have a size
of 1 µm to 1 mm. When adhesive composites that have been
produced from adhesive compositions that contain these
polystyrene beads are inductively heated, this leads to an
expansion of the polystyrene particles and thus to the
dissociation of the adhesive composite.
The adhesive composition according to the invention is
preferably used for adhesives, paints, sealants,
primers, matrix resins or casting resins.
A process for curing the adhesive composition according to
the invention to form adhesive joints consists in
inductively heating the adhesive composition by means of an
electrical field, magnetic field, electromagnetic field,
alternating electrical field, alternating magnetic field or
alternating electromagnetic field, to a temperature at
which the crosslinking of the adhesive composition starts.
This process has the advantage that the duration of the
inductive heating is normally in the range from seconds to
minutes, and is thus significantly shorter than in the
conventional thermal curing processes. Accordingly it is
particularly suitable for curing the adhesive compositions
according to the invention on sensitive objects. Also,
this process is very energy-efficient.
The curing process according to the invention may in
particular be carried out as described in Ortwin Hahn,
Andrea Kaimann, Adhäsion - Kleben und Dichten, 10/2001,
pp. 35 to 38 for adhesive compositions containing coarse
particulate fillers. The addition of curing catalysts and
activators, as is also described in unpublished
specification DE 10127704.0, is advantageous.
The adhesive composite obtained by the process according to
the invention for curing the adhesive composition according
to the invention contains at least one hardened adhesive
layer. In particular such an adhesive composite may be an
adhesive joint, a cast structural part, a sealing
structural part or a polymer laminate. The cured adhesive
layer may be a paint layer or a primer layer.
The process according to the invention for the thermal
dissociation of the adhesive composite that can be obtained
by curing the adhesive composition according to the
invention is carried out by inductively heating the
hardened layer of the adhesive composition by means of an
electrical field, magnetic field, electromagnetic field,
alternating electrical field, alternating magnetic field or
alternating electromagnetic field. If the adhesive
composition contains the crosslinking agent particles
according to the invention, then the hardened layer of the
adhesive composition is heated in the process according to
the invention to a temperature that lies above the ceiling
temperature of the crosslinking points. If the adhesive
composition contains filler particles and a thermally
labile substance, then the hardened layer of the adhesive
composition is heated inductively to a temperature at which
the thermally labile bonds of the thermally labile
substance or of the thermally labile group rupture.
In the process according to the invention for the thermal
dissociation of the hardened adhesive composites, the
filler particles are thus inductively heated, whereby a
chemical reaction is initiated in which either the
thermally labile substances effect a rupture of the
crosslinking points of the polymer network due to bond
rupture, formation of gas and/or swelling effects, or in
which, due to the inductive heating of the filler
particles, a bond rupture takes place at the crosslinking
points lying in the immediate vicinity of the filler
particles.
The dissociation of the adhesive composites according to
the invention thus takes place selectively by the action of
the high-frequency energy from a conventional induction
coil. Due to resultant eddy currents, particle movements
in the alternating field and hystoresis losses, the
metallic, ferromagnetic, ferrimagnetic, superparamagnetic
or paramagnetic filler particles according to the invention
present in the polymer network are heated. At the same
time there is also a heating of the polymer system in the
immediate environment of the filler particles. The
induction voltage is chosen so that the heat that is
generated is sufficient to dissociate the crosslinking
points in the polymer network and to destroy the latter
thermally in the case where heating is combined with
blowing agents. The induction frequencies are preferably
between a few kilohertz and about 35 megahertz. The
equipment, parameters and equipment adjustments required in
each case depend on the filler that is used and its content
in the polymer system. In particular, the particle size
distribution, Curie temperature, permeability, electrical
resistance, coefficient of thermal expansion and the
specific thermal capacity are quantities on which depends
the achievable temperature for a specific setting of the
equipment. The temperature required for the dissociation
depends on the thermal stability of the respective polymer
system and blowing agent. If the filler particles that are
used are chemically bound to the crosslinking sites of the
polymer system, then the filler itself is a constituent of
the polymer system. On account of the localised vicinity
of the chemical bonds to be separated to the filler
particles introduced according to the invention and
heatable by induction, the separation is in this case
particularly effective.
The process according to the invention for dissociating
adhesive composites may be used on bonded joints that
consist only of the adhesive itself according to the
invention, though there may also be used an adhesive primer
based on the adhesive compositions according to the
invention in combination with a commercially available
adhesive. In this case the dissociation of the composite
takes place selectively in the primer layer. The adhesive
remains on one of the two bonded parts.
If the adhesive composition according to the invention is a
paint that is to be inductively pickled, then in particular
adhesive compositions according to the invention are
advantageous in which the filler particles are bound to the
crosslinking agent component. This has the advantage that
no chemicals, no expensive equipment and no high labour
expenditure are necessary for the pickling. Furthermore
the paints that can be inductively pickled are particularly
suitable for sensitive substrates. As examples there may
be mentioned fibre-reinforced composite plastics, in which
the base polymers are damaged by the pickling chemicals, or
the fibres may be exposed or damaged during the grinding.
Both phenomena lead to an unallowable weakening of the
sensitive structural part.
The process according to the invention for the inductive
pickling is suitable in particular for carbon fibre-
reinforced structural parts of aircraft or glass fibre-
reinforced composites in ships' carcasses and wind power
blades.
Without restricting its general applicability, the adhesive
composition according to the invention, the process for
curing the latter to form an adhesive composite and the
dissociation of this adhesive composite are described in
more detail hereinafter with the aid of examples of use.
Example 1 - Curing and dissociation of a bonded joint with
inductively excitable filler particles bound to a
crosslinking agent
la) Nanoscale magnetite coated with silicon dioxide
43.3 g of iron(III) chloride hexahydrate are dissolved in
370 ml of water and freed from dissolved oxygen by passing
nitrogen through the solution. 15.9 g of iron(II) chloride
tetrahydrate are added and a solution of 25.6 g of sodium
hydroxide in 100 ml of water is added dropwise within
2 hours, with stirring, with a precision glass stirrer
under a flowing stream of nitrogen. A finely particulate
black precipitate of Fe3O4 is thereby formed. A solution of
22 g of Na2Si307 (annealing loss 17 wt.%) in 80 ml of hot
water is then added dropwise within 30 minutes. The
silicic acid is now precipitated, with further stirring, by
slow dropwise addition of hydrochloric acid (14 ml of 37%
hydrochloric acid made up to 50 ml with water). The
precipitate is filtered and made into a slurry five times
with distilled water and is in each case refiltered in
order to separate the sodium chloride formed. The
resulting material consists of agglomerated nanoparticles.
The primary particles have a diameter of about 8 nm
(determined by transmission electron microscopy) and the
agglomerates have a diameter of about 400 nm (determined by
light scattering).
lb) Modification of the nanoscale, inductively excitable
filler particles
20 g of the nanoscale magnetite produced according to
Example la with a residual moisture content of 40% or a
comparable material from another source is made into a
slurry with acetone, made up to a total volume of 300 ml,
acidified with 0.3 ml of conc, hydrochloric acid, following
which 15 g of epoxycyclohexyltrimethoxysilane are added.
The whole is stirred for 24 hours with a precision glass
stirrer and then dried in vacuo on a rotary evaporator.
The surface-modified filler carries cycloaliphatic epoxide
groups on the surface and is able to act as a crosslinking
agent in the adhesive system.
lc) Incorporation of the surface-modified filler into an
adhesive
10 g of 3,4-epoxycyclohexylmethyl-3',4'-epoxycyclohexane-
carboxylate, 10 g of cyclohexene oxide, 0.2 g of
(tolylcumyl) iodonium tetrakis(pentafluorophenyl) borate
and 0.2 g of ascorbic acid-6-hexadecanoate are stirred
until a homogeneous mixture is formed (base mixture
according to unpublished specification DE 10127704.0).
4 g of the surface-modified filler according to b) are
incorporated using a dissolver. After stirring for
15 minutes a homogeneous thixotropic mass has formed, which
is used hereinafter as adhesive.
1d) Bonding with inductive curing and re-dissociation of
the bonded joint
25 mm- wide and 4 mm- thick parts to be joined consisting
of glass fibre-reinforced polyester are bonded with the
adhesive produced according to c). For this, a part to be
joined is coated in the joining region with a 0.2 mm- thick
adhesive layer, the second part is placed thereon, and both
parts are fixed under a light pressure (ca. 0.02 N/mm2) .
The subsequent curing of the adhesive is carried out by
excitation with an M230 semiconductor generator from STS.
The excitation frequency of this generator is 300 kHz. A
coil with three windings and an internal diameter of 3 cm
is used for the inductive excitation of the adhesive in the
bonded joint. The adhesive surface is aligned in the
middle of the coil, perpendicular to the coil axis. The
adhesive is cured at an output of 1000 W and an action time
of 5 minutes, a firm joint thereby being obtained. This is
then dissociated within 60 secs by increasing the generator
output to 3000 W. In a comparison example without
inductively excitable nanoscale filler"particles, it is not
possible to cure the adhesive even at an output of 3 000 W
and an action time of 10 minutes.
Example 2 - Bonded joint that can be dissociated by an
inductively excitable blowing agent
2a) Formulation from magnetite powder and blowing agent
20 g of the material produced according to la) (residual
moisture of the filter cake 40%) or a nanoscale magnetite
powder obtained from another source is suspended in 100 ml
of ethanol and 20 g of oxy-bis(benzosulfohydrazide) are
added as blowing agent. The mixture is heated for 4 hours
at 70°C with stirring, and the solvent is then removed on a
rotary evaporator. The dry formulation is ground in a ball
mill for 5 minutes and then screened. The fraction with a
grain size of nominally less than 63 µm is used for the
further tests.
2b) Incorporation of the formulation from Example 2a) in
an adhesive
8 g of 3,4-epoxycyclohexylmethyl-3',4'-epoxycyclohexane-
carboxylate, 2 g of poly(tetrahydrofuran) of Mn=250, 0.1 g
of (tolylcumyl) iodonium tetrakis (pentafluorophenyl)
borate and 0.04 g of ascorbic acid-6-hexadecanoate are
stirred until the components have dissolved in one another
(base mixture according to unpublished specification
DE 10127704.0). 2 g of the formulation are then stirred
in, whereupon the material assumes a doughy consistency. A
part of the sample cures within 3 0 minutes at 90°C to form a
tack-free polymer.
2c) Bonding and re-dissociation of a plastics joint
25 mm- wide and 3 mm- thick polypropylene parts to be
joined are pretreated by fluorination according to the
prior art, coated with a ca. 0.2 mm- thick layer of the
inductively excitable formulation, following which a second
part is placed thereon and is cured under a light pressure
(ca. 0.02 N/mm2) for 3 0 minutes in an oven at 90°C. The
subsequent separation of the joint is carried out by
excitation with an M230 semiconductor generator from STS.
The excitation frequency of this generator is 300 kHz. A
coil with three windings and an internal diameter of 3 cm
is used for the inductive excitation of the adhesive in the
bond joint. The adhesive surface is aligned in the middle
of the coil, perpendicular to the coil axis. With an
output of 1500 W and an action time of 25 secs, the blowing
agent has decomposed and thereby dissociated the bonded
joint. In a comparison example without the nanoscale
magnetite powder, the bonded joint cannot be dissoicated
even under the action of an output of 3 000 W for 2 minutes.
The analytical data of the iron oxide-silicon dioxide
composite particles used in Examples 3 to 6 are shown in
Table 1. The production of these particles is described in
DE 10140089.6.
Example 3 - Dissociation of a glass bond based on an
adhesive with inductively excitable blowing agent
3a) Formulation from composite particles produced by flame
pyrolysis and a binder
25 g of nanoscale composite particles produced by flame
pyrolysis and consisting of silicon dioxide and iron oxide
having the properties shown in Table 1 are suspended in
100 ml of ethanol and 20 g of oxy-bis(benzosulfohydrazide)
are added as blowing agent. The mixture is heated for
5 hours at 60°C with stirring, and the solvent is then
removed on a rotary evaporator. The dry formulation is
ground in a ball mill for 3 minutes and then screened. The
fraction with a grain size of nominally less than 63 µm is
used for the further tests.
3b) Incorporation of the formulation from Example 3a) in
an adhesive, and adhesive tests
3 00 g of the moisture-hardening one-component polyurethane
adhesive Dinitrol PUR 501 FC (Dinol GmbH) are modified in a
Planimax (Molteni) mixer provided with kneading hooks, with
10 g of the formulation produced according to Example 3a
and consisting of blowing agent and inductively excitable
nanofiller. The mixture is kneaded for 15 minutes at
setting 1 (150 rpm) in a dry atmosphere.
A thick layer bond between a sand-blasted and degreased
aluminium sheet and a 3 mm- thick float glass panel is
prepared using the thereby modified adhesive. The overlap
length is 25 mm and the adhesive layer thickness is 3 mm.
After a curing time of 1 week at 25°C and 50% relative
atmospheric humidity the joint is re-separated by inductive
excitation. The separation of the joint is carried out by
excitation with an M23 0 semiconductor generator from STS.
The excitation frequency of this generator is 300 kHz. A
coil with three windings and an internal diameter of 3 cm
is used for the inductive excitation of the adhesive in the
bonded joint. The adhesive surface is aligned in the
middle of the coil, perpendicular to the coil axis. At an
output of 3000 W and an action time of 2 minutes the
adhesive is destroyed by the expansion of the blowing
agent. The two joined parts can easily be separated from
one another.
Example 4 - Dissociable bonded joint based on an
inductively dissociable adhesive primer
5 g of the formulation prepared according to Example 3a and
consisting of blowing agent and inductively excitable
nanofiller are stirred into 200 g of the Sika-Primer 206G+P
(Sika AG) adhesive primer. The primer is applied to a
sand-blasted and degreased aluminium sheet so as to cover
the latter. After an aeration time of 1 hour the sheet
pretreated in this way is bonded with a 3 mm- thick layer
of beech plywood. Sikaflex 254 (Sika AG) is applied as
adhesive in a thickness of 3 mm, and the overlap length is
25 mm. The adhesive hardens within 1 week at a relative
atmospheric humidity of 50% and at 25°C. The joint is then
re-separated by inductive excitation. The excitation of
the adhesive for the separation is carried out with an M230
semiconductor generator from STS. The excitation frequency
of this generator is 300 kHz. A coil with three windings
and an internal diameter of 3 cm is used for the inductive
excitation of the adhesive in the bonded joint. The
adhesive surface is aligned in the middle of the coil,
perpendicular to the coil axis.
At an output of 3 000 W and an action time of 2 minutes the
adhesive primer applied to the aluminium side is destroyed
by the expansion of the blowing agent. The parts of the
joint can easily be separated from one another, the
adhesive remaining selectively on the plywood.
Example 5 - Curing an elastic adhesive and testing the
adhesive properties
The elastic adhesive Elastosol M83 (Tivoli, Hamburg) is a
one-component, heat-curing metal adhesive based on
polybutadiene. On the basis of a comparison of the curing
in a conventional oven with the inductive curing according
to the invention, it will be shown that equivalent bonding
results are achieved with both types of curing. In this
connection the inductive curing occurs more rapidly.
25 g of the iron oxide-silicon dioxide composite particles
according to Table 1 are incorporated in 250 g of the
adhesive Elastosol M83 using a Planimax mixer (Molteni)
equipped with kneading hooks. Kneading is first of all
carried out for 5 minutes at 150 revolutions per minute and
then for a further 30 minutes at 450 rpm (setting 3). The
mixture is then kneaded for a further 5 minutes in vacuo to
degass it (setting 3). The material according to the
invention that is thus obtained is used for the adhesive
tests.
In order to check the adhesive properties, tensile/shear
samples are produced on the basis of DIN EN 1465, one part
to be joined consisting of 1.15 mm- thick rolled aluminium
sheet material (AlMgo.4Si12) and another part to be joined
consisting of 4 mm- thick, glass fibre-reinforced
polypropylene. The aluminium is ground and degreased with
butanone. The polypropylene is pretreated in a low-
pressure plasma with air as working gas.
Adhesive samples are first of all prepared with the
modified adhesive according to the invention and
inductively hardened. The curing of the adhesive is
carried out by excitation with an M23 0 semiconductor
generator from STS. A water-cooled flat coil with three
windings and a diameter of 8 cm is used for the inductive
excitation of the adhesive in the bonded joint. The coil
is placed on the joined part of polypropylene and the
adhesive is cured at an output of 1000 W and an action time
of 10 minutes The samples have a tensile-shear strength of
10.4 ± 0.6 MPa, with a cohesive fracture of the adhesive.
For purposes of comparison, tensile/shear samples are
prepared with the unmodified adhesive. In this case the
adhesive is cured in a conventional manner according to the
manufacturer's instructions. The curing is carried out
over 3 0 minutes at 180°C in an oven. The tensile-shear
strength of these samples is 10.1 ± 0.4 MPa.
Example 6 - Modification of a melt adhesive for the
selective dissociation of bonded joints
The melt adhesive B40166 (Heinrich Büuhnen GmbH)is modified
with 7 wt.% of iron oxide-silicon dioxide composite
particles according to Table 1 in a Brabender double-screw
extruder at a screw speed of 60 rpm and a screw temperature
of 22 0°C in all heating zones. The melt adhesive is
granulated and applied with an HB 500 application device to
5 mm- thick beech plywood. A second piece of beech plywood
is immediately pressed onto the melt adhesive. The joint
is firm within 1 minute. The dissociation of the bonded
joint is carried out inductively with the M230
semiconductor generator from STS and a water-cooled flat
coil with three windings and a diameter of 8 cm. The coil
is placed on the plywood and an output of 3000 W is
adjusted at the semiconductor generator. After an action
time of 60 seconds the two plywood plates can be taken
apart and, after renewed inductive heating, can be rebonded
to one another.
WE CLAIM:
Adhesive composition for the production of thermosets, the
composition being able to be heated by means of an electrical
field, magnetic field, electromagnetic field, alternating
electrical field, alternating magnetic field or alternating
electromagnetic field and containing a polymer, a polymer mixture
or a reaction resin, and crosslinking agent particles, wherein
the crosslinking agent particles comprise filler particles that
are ferromagnetic, ferrimagnetic, superparamagnetic or
paramagnetic and crosslinking agent units chemically bound to
these filler particles.
2. Adhesive composition as claimed in claim 1, wherein the
content of crosslinking agent particles is 0.1 wt. % to 80 wt.X,
preferably 0.5 wt.X to 40 wt.% and particularly preferably 1 wt.
% to 30 wt. X.
3. Adhesive composition as claimed in claim 1 or 2, wherein
the crosslinking agent particles have average primary particle
sizes between 2 nm and 1000 nm, preferably between 2 nm and 500
nm and particularly preferably between 2 nm and 100 nm.
4. Adhesive composition as claimed in claims 1 to 3, wherein
the crosslinking agent particles have, referred to their surface,
-2
at least 0.00001 mmole x m of functional groups with a
crosslinking action.
5. Adhesive composition as claimed in claims 1 to 4, wherein
the filler particles are surface-modified.
6. Adhesive composition as claimed in claims i to 5, wherein
the filler particles are selected from the group comprising iron,
iron alloys and iron-containing metal oxides.
7. Adhesive composition as claimed in claim 9, wherein the
filler particles have a core-shell structure and are produced by
sol-gel processes or from the reaction of nanoscale iron oxide
with sodium silicate.
3. Adhesive composition as claimed in claim 5» wherein the
filler particles ,are superparamagnetic iron oxide-silicon dioxide
composite particles produced by flame pyrolysis.
9. Adhesive composition as claimed in claims 1 to 8, wherein
the crosslinking agent units are bound via a thermally labile
group to the filler particles.
10. Adhesive composition as claimed in claim 9 wherein the
thermally labile group is an azo group, a carbonate group or an
ethylene group with sterically demanding substituents.
11. Adhesive composition for the production of thermosets as
claimed in claims 1 to 8 wherein it additionally contains a
thermally labile substance.
12. Adhesive composition as claimed in claim 11 wherein the
thermally labile substance has average particle sizes between 2 nm
and 100 µm preferably between 2 nm and 1 µm and particularly
preferably between 2 nm and 200 nm.
13. Adhesive composition as claimed in claim 11 or 12,
wherein the thermally labile substance is a blowing agent that
forms gas under the action of heat, in which the gas formation
temperature is higher than the temperature at which the
crosslinking of the adhesive composition starts.
14. Adhesive composition as claimed in claim 13, wherein the
blowing agent is selected from the group comprising
azodicarbonamide and sulfohydrazides, in particular toluene
sulfohydrazide and oxygen-bis (benzosulfohydrazide>.
15. Adhesive composition as claimed in claim 13 or 14 wherein
collective particles are included that contain the blowing agent
and the filler particles and are obtainable by precipitation,
compression, microencapsulation or bonding of blowing agent and
filler particles with a polymer.
16. Adhesive composition as claimed in claim 15, wherein the
polymer for the formation of the collective particle, is
expandable polystyrene.
17. Process for the curing of an adhesive composition as
claimed in claims 1 to 16, wherein the adhesive composition is
inductively heated by means of an electrical field, magnetic
field, electromagnetic field, alternating electrical field,
alternating magnetic field or alternating electromagnetic field
to a temperature at which the crosslinking of the adhesive
composition starts.
18. Adhesive composite that comprises at least one adhesive
layer that is obtainable by curing the adhesive composition as
claimed in one or more of claims 1 to 16.
19. Adhesive composite as claimed in claim 18 wherein the at
least one adhesive layer is a paint layer or primer layer.
20. Adhesive composite as claimed in claim 18 or 19 that is
a bonded joint, a cast structural part, a sealed structural part
or a polymer laminate.
21. Process for the thermal dissociation of an adhesive
composite that can be obtained by curing the adhesive composition
as claimed in claims 1 to 8, wherein the hardened layer of the
adhesive composition is heated by means of an electrical field,
magnetic field, electromagnetic fields alternating electrical
field, alternating magnetic field or alternating electromagnetic
field to a temperature that lies above the ceiling temperature of
the crosslinking points.
22. Process for the thermal dissociation of an adhesive
composite that can be obtained by curing the adhesive composition
as claimed in claims 9 to 16, wherein the hardened layer of the
adhesive composition is heated by means of an electrical field,
magnetic field, electromagnetic field, alternating electrical
field, alternatic magnetic field or alternating electrommagnetic
field to a temperature at which the thermally labile bonds of a
thermally labile substance and/or thermally labile group rupture.
Adhesive composition for the production of thermosests, the
composition being able to be heated by means of an electrical
field, magnetic field, electromagnetic field, alternating
electrical field, alternating magnetic field or alternating
electromagnetic field and containing a polymer, a polymer
mixture or a reaction resin, and crosslinking agent particles,
wherein the crosslinking agent particles comprise filler
particles that are ferromagnetic, ferrimagnetic,
superparamagnetic or paramagnetic and crosslinking agent units
chemically bound to these filler particles.

Documents:

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Patent Number

224705

Indian Patent Application Number

00611/KOLNP/2004

PG Journal Number

43/2008

Publication Date

24-Oct-2008

Grant Date

22-Oct-2008

Date of Filing

12-May-2004

Name of Patentee

DEGUSSA AG

Applicant Address

BENNIGSENPLATZ 1, DE-40474 DUSSELDORF

Inventors:

#	Inventor's Name	Inventor's Address
1	KOLBE, DR. JANA	HEMMSTRASSE 359, DE-28215 BREMEN
2	PRIDÖHL, DR. MARKUS	TORSBYVÄGEN 25, DE-63538 GROßKROTZENBURG
3	ZIMMERMANN, GUIDO	CASTELLSTRASSE 19A, DE-63454 HANAU
4	HARTWIG, DR. ANDREAS	BEEKSTRASSE 10D, DE-27721 RITTERHUDE
5	BORN, DR. ERWIN	DOHLENDAMM 3, DE-28359 BREMEN
6	KOWALIK, DR. THOMAS	FLEETRADE 15B, DE-28207 BREMEN
7	POPP, DR. MATTHIAS	ARENSBURGSTRASSE 55, DE-28211 BREMEN
8	SEBALD, MONIKA	ANNA-WEGENER-WEG 38, DE-28357 BREMEN
9	SCHORSCH, OLIVER	EDERWEG 15, DE-28205 BREMEN
10	HEBERER, STEFAN	WIESENBORNSTRASSE 3, DE-63571 GELNHAUSEN

PCT International Classification Number

C09J 11/04

PCT International Application Number

PCT/EP02/12610

PCT International Filing date

2002-11-12

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	101 55 614.4	2001-11-13	Germany
2	102 10 661.4	2002-03-12	Germany