EP0753358B1 - Method of painting elements made from plastics, and elements formed thereby - Google Patents
Method of painting elements made from plastics, and elements formed thereby Download PDFInfo
- Publication number
- EP0753358B1 EP0753358B1 EP96110839A EP96110839A EP0753358B1 EP 0753358 B1 EP0753358 B1 EP 0753358B1 EP 96110839 A EP96110839 A EP 96110839A EP 96110839 A EP96110839 A EP 96110839A EP 0753358 B1 EP0753358 B1 EP 0753358B1
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- EP
- European Patent Office
- Prior art keywords
- layer
- polymerisable
- painted
- paint
- predetermined temperature
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000004033 plastic Substances 0.000 title claims description 21
- 229920003023 plastic Polymers 0.000 title claims description 21
- 238000000034 method Methods 0.000 title claims description 17
- 238000010422 painting Methods 0.000 title claims description 5
- 239000000463 material Substances 0.000 claims description 54
- 239000003973 paint Substances 0.000 claims description 39
- 239000002131 composite material Substances 0.000 claims description 12
- 239000000178 monomer Substances 0.000 claims description 12
- 238000010438 heat treatment Methods 0.000 claims description 11
- 229920005989 resin Polymers 0.000 claims description 11
- 239000011347 resin Substances 0.000 claims description 11
- 239000002318 adhesion promoter Substances 0.000 claims description 7
- 239000004814 polyurethane Substances 0.000 claims description 7
- 229920002635 polyurethane Polymers 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 7
- 238000009834 vaporization Methods 0.000 claims description 7
- 229920001187 thermosetting polymer Polymers 0.000 claims description 6
- 229920000728 polyester Polymers 0.000 claims description 5
- 229920001567 vinyl ester resin Polymers 0.000 claims description 5
- 229920001225 polyester resin Polymers 0.000 claims description 4
- 239000004645 polyester resin Substances 0.000 claims description 3
- 230000004888 barrier function Effects 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims 2
- 239000010410 layer Substances 0.000 description 68
- 239000011148 porous material Substances 0.000 description 13
- 239000007789 gas Substances 0.000 description 9
- 238000000576 coating method Methods 0.000 description 8
- 239000011248 coating agent Substances 0.000 description 7
- 229910000831 Steel Inorganic materials 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000010959 steel Substances 0.000 description 4
- 238000000748 compression moulding Methods 0.000 description 2
- 210000003660 reticulum Anatomy 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000271 Kevlar® Polymers 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000004761 kevlar Substances 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000007591 painting process Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
- B05D7/50—Multilayers
- B05D7/56—Three layers or more
- B05D7/58—No clear coat specified
- B05D7/586—No clear coat specified each layer being cured, at least partially, separately
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D1/00—Processes for applying liquids or other fluent materials
- B05D1/02—Processes for applying liquids or other fluent materials performed by spraying
- B05D1/04—Processes for applying liquids or other fluent materials performed by spraying involving the use of an electrostatic field
- B05D1/045—Processes for applying liquids or other fluent materials performed by spraying involving the use of an electrostatic field on non-conductive substrates
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
- B05D7/02—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials to macromolecular substances, e.g. rubber
Definitions
- the present invention concerns an improved method of painting applicable to elements formed from synthetic plastics materials, in particular, motor-vehicle body components made from composites, which avoids the risk of bubbles and/or blisters forming in the layer/layers of paint/paints.
- the invention also relates to elements formed from painted plastics material, which have a high quality of surface finish and do not require, except in exceptional cases, subsequent repairs to the paintwork.
- a base layer of an electroconductive material is applied directly to the surfaces of the plastics elements to be painted, this base usually comprising a single-component conductive primer which polymerises at a relatively high temperature (approximately 150°C).
- the primer is spread in a layer of predetermined thickness (approximately 30 microns) and the treated element is then stoved in an oven, causing polymerisation of the primer layer which hardens to form a porous, transparent, conductive film on the surface of the plastics element to be painted.
- the element may then be painted by conventional methods as if it were an element made from sheet steel; this also improves the adhesion of the layers of paint applied successively to the surface of the element.
- the elements are again stoved at a high temperature (150°C) to cause the polymerisation of the paint layers.
- the aim of the invention is to provide an improved method of painting elements made from synthetic plastics materials, in particular vehicle body parts made from composites, which does not have the disadvantages described, in particular being free from the risk of bubbles forming in the paint layer during the stoving stage.
- the invention therefore provides a method of painting applicable to elements made from synthetic plastics material, in particular motor vehicle parts made from composites, as claimed in claim 1. Therefore, firstly, at least one base layer of a predetermined thickness of a polymerisable electroconductive material is applied to a surface of a said element to be painted and, subsequently at least one layer of paint is applied on top of the said base layer of polymerisable material; then
- the said element to be painted is formed from a material based on thermosetting vinyl ester/polyester resins
- the said second polymerisable material is constituted by a catalysed two-component polyurethane transparent paint which is completely polymerisable by heating to just 60°C.
- the said second polymerisable material is applied to a layer formed by a polyester-based adhesion promoter which is applied directly to the surface to be painted.
- the invention also relates to a painted element as claimed in Claim 8.
- the application of the catalysed two-component polyurethane paint layer directly to the surface to be painted (with the interposition solely of the adhesion promoter) and its polymerisation before the application of the conventional layers of primer and paint to the surface to be painted allows a gas-impermeable layer to be formed on the surface itself, forming a gas-tight seal over the surface pores which may contain unpolymerised or partially-polymerised monomers.
- the gases produced are no longer able to reach the painted surface and pass through the porous primer layer to penetrate the layers of paint being polymerised and so form the known bubbles.
- the polymerisation of the layer of gas-impermeable material at a low temperature (about 60°C), by virtue of the use of catalysed paints, also guarantees that no monomers can vaporise during the polymerisation of this sealing layer, risking localised damage in the layer which is still being polymerised, which could mean that the layer itself is not completely impermeable.
- the reference numeral 1 indicates an element formed from a synthetic plastics material, for example, a panel pressed from a composite material and forming a vehicle body part, for example, of a motor vehicle, such as a bonnet, a door, etc.
- the composites are considered, for simplicity, as a subclass of synthetic materials being, as is known, constituted by a reinforcing agent (glass, carbon, kevlar fibres, etc, regardless of how it is formed and distributed), encapsulated in a matrix constituted by one or more synthetic plastics resins obtained by the polymerisation of one or more monomers.
- the panel or element 1 has a surface 2 covered by a paint coating 3 (possibly constituted by a plurality of superposed thinner layers of diverse materials); the surface 2 also contains pores 4 (only one of which is illustrated on an enlarged scale in Figure 1), at least some of which are partially filled with grains 5 of unpolymerised or only partially polymerised monomers; the grains 5 are formed from the same monomers as those used to form the resin/resins constituting the synthetic plastics base material from which (with the addition of the fillers) the element or panel 1 is made, and are the inevitable result of the known process for forming the panel or element 1 which is, for example, obtained by injection moulding, compression moulding, or injection-compression moulding.
- the resin/resins forming the element or panel 1 are thermosetting vinyl ester/polyester resins as the element/panel 1 is moulded from a composite of the SMC, BMC or similar type.
- the grain 5 vaporises creating gases (shown by the arrows 6) which, together with any air which may be trapped in the pore 4, expand and leave the pore 4, causing the coating 3 to swell which, as it is in the polymerising phase, is soft and plastic, although already mostly impermeable to gases; the gases 6 are thus not able to escape and they collect above the pore 4 and below the coating 3, creating a bubble 7.
- the sizes of the bubbles 7 are an order of magnitude greater than those in the pores 4, which may vary from several microns to several millimetres: consequently, the bubbles 7 which form are between 1 and 10 millimetres in diameter or more.
- a coating 3a is formed according to the invention on the surface 2 and, starting with the layer adjacent the surface 2, comprises two superimposed films B and A; the film A corresponds to conventional coatings, such as that in Figure 1, while the film B includes, in turn, a first continuous layer 10 applied directly to the surface 2 to cover it completely, being approximately 30 microns thick and formed from a polyester-based adhesion promoter ("Barrier"), for example, 487567 from the firm PPG Industries Inc, USA, and a second layer 11, also continuous and applied directly to the layer 10 so as to cover the surface 2 completely, being between 30 and 40 microns thick and formed from a material which polymerises at low temperature (approximately 60°C) and is impermeable to gaseous substances such that the layer 10 is completely gas-impermeable.
- Barrier polyester-based adhesion promoter
- second layer 11 also continuous and applied directly to the layer 10 so as to cover the surface 2 completely, being between 30 and 40 microns thick and formed from a material which polymerises
- the layer 11 is formed from a catalysed two-component transparent polyurethane paint, such as, for example, 228003 obtained from PPG Industries Inc.
- the film A instead, is, as already stated, constituted by a conventional multi-layer coating including, in the present case: a first layer 12 of thickness which may vary between 20 and 30 microns formed from an electrically-conductive polymerisable primer of the single-component type, for example, 487538, also from PPG Industries Inc, having a stoving temperature (for polymerisation) of about 150°C; a second layer 13, approximately 40 microns thick, formed from an undercoat paint, for example, "base coat” 400085/1 from HERBERTS GmbH, WUPPERTAL (D); a third layer 14, approximately 30 microns thick, formed from enamel and defining the real paint layer; and a surface layer 15 of approximately 30 microns thick, formed from a protective transparent polymer, for example, a "lacquer" of any known type.
- the layer 10 is first of all applied, for example, by spraying to the surface 2 of the untreated element or panel 1 to be painted and then the layer 11 of two-component paint, which is applied by a "wet on wet” technique, that is, while the underlying film of material just applied is still wet due to the, as yet, incomplete evaporation of the solvent used.
- the element 1, with only the layers 10 and 11 covering the surface 2 completely, is then stoved in an oven at a temperature which causes the rapid polymerisation of the material forming the layer 11; since one is dealing with a catalysed paint, the latter polymerises completely in approximately 45 minutes on heating of the element 1 to merely 60°C.
- the element 1 is cooled and the layer 12 of conductive primer is first applied thereto in a known way followed by the layers 13, 14, 15 of paint proper; these layers, starting from the base layer 12, are not however applied directly to the surface 2, as in the prior art, but to the layer 11 which, as already said, is completely impermeable to gases when fully polymerised; instead, the layer 12, which acts as a base for the in-line application of the three layers of paint 13, 14 and 15 by the same known methods as for body parts made from sheet steel is, as is known, porous and therefore permeable to gaseous substances which are able to diffuse through it, in the direction of the thickness, as already described in Figure 1.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Laminated Bodies (AREA)
Description
- The present invention concerns an improved method of painting applicable to elements formed from synthetic plastics materials, in particular, motor-vehicle body components made from composites, which avoids the risk of bubbles and/or blisters forming in the layer/layers of paint/paints. The invention also relates to elements formed from painted plastics material, which have a high quality of surface finish and do not require, except in exceptional cases, subsequent repairs to the paintwork.
- It is known in the motor vehicle industry, that vehicle body components (bonnets, doors, etc) made from synthetic plastic materials are being used increasingly and these may be formed in complex shapes and/or with low weights, both of which factors are impossible to achieve with sheet steel elements of substantially the same dimensions. Composites such as SMC, BMC, etc based on thermosetting plastics resins of the vinyl ester/polyester type are preferably used to make such components.
- Once moulded, such components must be painted with the same paints and, substantially, the same production cycle as sheet-steel parts in order to ensure perfect aesthetic conformity between parts of the same motor vehicle made from different materials. To this end, a base layer of an electroconductive material is applied directly to the surfaces of the plastics elements to be painted, this base usually comprising a single-component conductive primer which polymerises at a relatively high temperature (approximately 150°C).
- Typically, the primer is spread in a layer of predetermined thickness (approximately 30 microns) and the treated element is then stoved in an oven, causing polymerisation of the primer layer which hardens to form a porous, transparent, conductive film on the surface of the plastics element to be painted. By virtue of the conductivity of the primer the element may then be painted by conventional methods as if it were an element made from sheet steel; this also improves the adhesion of the layers of paint applied successively to the surface of the element. After all the paint/paints have been applied, the elements are again stoved at a high temperature (150°C) to cause the polymerisation of the paint layers.
- However, during the painting process described and, in particular, during the final stage of stoving of the painted elements, problems, such as the formation of bubbles or blisters in the paint layer, frequently arise; this occurs particularly frequently in the case of vehicle body parts formed from composites based on thermosetting resins such as BMC and SMC. This problem requires the elements upon which surface bubbles have developed to be repaired manually by means of sanding to remove the layer of paint ruined by the bubble, filling and repainting: this is slow and involves a significant increase in manufacturing costs; in addition, during the subsequent stoving of the repainted part, the problem of bubbles forming in the paint layer may arise again leading, in the most serious cases, to the component being discarded.
- The problems described are the reason for the lack of extensive use, in the motor vehicle industry, of vehicle body parts made from composites, which use is instead limited to small-scale production, to cover so-called "niche" productions, such as special vehicles (convertibles, single-compartment family vehicles etc).
- The problem is not solved by US-I-T982004 which provides a method wherein two primers, one of which able to give raise to a gas impermeable layer, are polymerized at the same temperature.
- The aim of the invention is to provide an improved method of painting elements made from synthetic plastics materials, in particular vehicle body parts made from composites, which does not have the disadvantages described, in particular being free from the risk of bubbles forming in the paint layer during the stoving stage.
- On this basis, the invention therefore provides a method of painting applicable to elements made from synthetic plastics material, in particular motor vehicle parts made from composites, as claimed in
claim 1. Therefore, firstly, at least one base layer of a predetermined thickness of a polymerisable electroconductive material is applied to a surface of a said element to be painted and, subsequently at least one layer of paint is applied on top of the said base layer of polymerisable material; then - the element is brought to a first predetermined temperature to cause the polymerisation of the said base layer of polymerisable electroconductive material;
- (a) - applying a continuous layer of a second polymerisable material to the said surface to be painted, the said second material being of a type which, once polymerised, can form a layer which is impervious to any gaseous substance and which is completely polymerisable by heating to a second predetermined temperature below both the said first predetermined temperature and the lowest temperature of vaporisation of the monomers forming the said synthetic plastics material constituting the said element to be painted;
- (b) - heating the element, with the said surface to be painted covered with the said layer of the second polymerisable material, to the said second predetermined temperature until the said second polymerisable material is completely polymerised;
- In particular, the said element to be painted is formed from a material based on thermosetting vinyl ester/polyester resins, and the said second polymerisable material is constituted by a catalysed two-component polyurethane transparent paint which is completely polymerisable by heating to just 60°C. The said second polymerisable material is applied to a layer formed by a polyester-based adhesion promoter which is applied directly to the surface to be painted.
- The invention also relates to a painted element as claimed in Claim 8.
- In this way, any risk that bubbles will form in the paint layer as a result of the final stoving to which the painted elements must be subjected to polymerise the layer/layers of paint applied is completely avoided. In fact, the Applicant has established by extensive experimentation that the formation of bubbles in the paint, a well known disadvantage which has until now greatly limited the extensive use of painted composite elements in a vehicle body, is due to the vaporisation, during stoving (which occurs at approximately 150°C), of a small proportion of the monomers, forming the resin/resins from which the element to be painted is formed which have not polymerised or are only partly polymerised and which, during the pressing, remain trapped in micropores, invisible to the naked eye, close to the surface of the element and in communication with the exterior.
- However, the application of the catalysed two-component polyurethane paint layer directly to the surface to be painted (with the interposition solely of the adhesion promoter) and its polymerisation before the application of the conventional layers of primer and paint to the surface to be painted allows a gas-impermeable layer to be formed on the surface itself, forming a gas-tight seal over the surface pores which may contain unpolymerised or partially-polymerised monomers.
- Consequently, when these vaporise during the final stoving of the painted element, the gases produced are no longer able to reach the painted surface and pass through the porous primer layer to penetrate the layers of paint being polymerised and so form the known bubbles. The polymerisation of the layer of gas-impermeable material at a low temperature (about 60°C), by virtue of the use of catalysed paints, also guarantees that no monomers can vaporise during the polymerisation of this sealing layer, risking localised damage in the layer which is still being polymerised, which could mean that the layer itself is not completely impermeable.
- These and other characteristics of the invention will become clearer from the following description of a preferred embodiment, given by way of non-limitative example, with reference to the accompanying drawings, in which:
- Figure 1 represents schematically the mechanism by which bubbles are formed in a layer of paint applied to a surface of an element made from plastics material; and
- Figure 2 represents schematically in section the structure of a plastics element painted according to the invention.
- With reference to Figures 1 and 2, the
reference numeral 1 indicates an element formed from a synthetic plastics material, for example, a panel pressed from a composite material and forming a vehicle body part, for example, of a motor vehicle, such as a bonnet, a door, etc. Here and in the following description, the composites are considered, for simplicity, as a subclass of synthetic materials being, as is known, constituted by a reinforcing agent (glass, carbon, kevlar fibres, etc, regardless of how it is formed and distributed), encapsulated in a matrix constituted by one or more synthetic plastics resins obtained by the polymerisation of one or more monomers. - The panel or
element 1 has asurface 2 covered by a paint coating 3 (possibly constituted by a plurality of superposed thinner layers of diverse materials); thesurface 2 also contains pores 4 (only one of which is illustrated on an enlarged scale in Figure 1), at least some of which are partially filled withgrains 5 of unpolymerised or only partially polymerised monomers; thegrains 5 are formed from the same monomers as those used to form the resin/resins constituting the synthetic plastics base material from which (with the addition of the fillers) the element orpanel 1 is made, and are the inevitable result of the known process for forming the panel orelement 1 which is, for example, obtained by injection moulding, compression moulding, or injection-compression moulding. - In the present case described, which concerns
elements 1 intended for motor vehicle bodies, the resin/resins forming the element orpanel 1 are thermosetting vinyl ester/polyester resins as the element/panel 1 is moulded from a composite of the SMC, BMC or similar type. - As determined by the Applicant, because of the microstructure of the panel/
element 1, when the paintedelement 1 is heated to polymerise the multi-layered coating 3, thegrain 5 vaporises creating gases (shown by the arrows 6) which, together with any air which may be trapped in thepore 4, expand and leave thepore 4, causing the coating 3 to swell which, as it is in the polymerising phase, is soft and plastic, although already mostly impermeable to gases; thegases 6 are thus not able to escape and they collect above thepore 4 and below the coating 3, creating a bubble 7. It has been determined that the sizes of the bubbles 7 are an order of magnitude greater than those in thepores 4, which may vary from several microns to several millimetres: consequently, the bubbles 7 which form are between 1 and 10 millimetres in diameter or more. - This fact confirms the validity of the interpretive model described above: if, in fact, the formation of the bubbles 7 were not due primarily to the vaporisation of monomers which are not 100% polymerised within the
pores 4, the size of the bubbles would in practice be limited to 5/7 of those within the pores 4 (a value corresponding to the variation in volume of the air in thepores 4 caused by thermal expansion) and, consequently, only extremely small bubbles would form. In addition, the model is further confirmed by the fact that, in current practice, bubbles also form again at exactly the same places onelements 1 that have already experienced the phenomenon and which have been repaired (by sanding, filling and repainting of the places where bubbles formed), as soon as the piece is heated again to polymerise the paint in the repaired areas. - With reference to Figure 2, the known phenomenon illustrated in Figure 1 is avoided, according to the invention, by means of a particular structuring of the multi-layered coating 3. In practice, a
coating 3a is formed according to the invention on thesurface 2 and, starting with the layer adjacent thesurface 2, comprises two superimposed films B and A; the film A corresponds to conventional coatings, such as that in Figure 1, while the film B includes, in turn, a firstcontinuous layer 10 applied directly to thesurface 2 to cover it completely, being approximately 30 microns thick and formed from a polyester-based adhesion promoter ("Barrier"), for example, 487567 from the firm PPG Industries Inc, USA, and asecond layer 11, also continuous and applied directly to thelayer 10 so as to cover thesurface 2 completely, being between 30 and 40 microns thick and formed from a material which polymerises at low temperature (approximately 60°C) and is impermeable to gaseous substances such that thelayer 10 is completely gas-impermeable. - In the present case, the
layer 11 is formed from a catalysed two-component transparent polyurethane paint, such as, for example, 228003 obtained from PPG Industries Inc. The film A, instead, is, as already stated, constituted by a conventional multi-layer coating including, in the present case: afirst layer 12 of thickness which may vary between 20 and 30 microns formed from an electrically-conductive polymerisable primer of the single-component type, for example, 487538, also from PPG Industries Inc, having a stoving temperature (for polymerisation) of about 150°C; asecond layer 13, approximately 40 microns thick, formed from an undercoat paint, for example, "base coat" 400085/1 from HERBERTS GmbH, WUPPERTAL (D); athird layer 14, approximately 30 microns thick, formed from enamel and defining the real paint layer; and asurface layer 15 of approximately 30 microns thick, formed from a protective transparent polymer, for example, a "lacquer" of any known type. - According to the invention, the
layer 10 is first of all applied, for example, by spraying to thesurface 2 of the untreated element orpanel 1 to be painted and then thelayer 11 of two-component paint, which is applied by a "wet on wet" technique, that is, while the underlying film of material just applied is still wet due to the, as yet, incomplete evaporation of the solvent used. Theelement 1, with only thelayers surface 2 completely, is then stoved in an oven at a temperature which causes the rapid polymerisation of the material forming thelayer 11; since one is dealing with a catalysed paint, the latter polymerises completely in approximately 45 minutes on heating of theelement 1 to merely 60°C. At such a low temperature, which is certainly below the lowest temperature of vaporisation of any monomers in thepores 4, these latter are not able to generate any gas whereby thelayer 11 polymerises completely, thereby becoming impermeable to any gaseous substance rapidly and without any damage. - Once the polymerisation of the
layer 11 is complete, theelement 1 is cooled and thelayer 12 of conductive primer is first applied thereto in a known way followed by thelayers base layer 12, are not however applied directly to thesurface 2, as in the prior art, but to thelayer 11 which, as already said, is completely impermeable to gases when fully polymerised; instead, thelayer 12, which acts as a base for the in-line application of the three layers ofpaint - Therefore, when the stoving stage necessary for polymerisation of the
layer 12 is reached (as well as any subsequent stoving to cause the other layers of the film A to polymerise, whether separately or together), which step is executed by bringing theelement 1 to a temperature of 140-160°C (on average 150°C) for approximately 30 minutes (always to a temperature much higher than that for the polymerisation of the layer 11), the gases which arise in the pores 4 (Figure 2) as a consequence of the vaporisation of the monomers therein, leave thepores 4 to diffuse towards the film A but, before reaching theporous layer 12 which is still polymerising, encounter the gas-impermeable layer 11 which is already completely polymerised and therefore very rigid and of high mechanical strength. Consequently, thegases 6 are sealed in thepores 4, below thelayer 11 and are therefore prevented from deforming the plastic layers 12-15 and creating bubbles 7. Any risk of the formation thereof is therefore avoided.
Claims (9)
- A method of painting applicable to elements formed from synthetic plastics materials, in particular components of motor vehicles formed from composites, characterized by comprising the steps of:applying to a surface (2) of a said element (1) to be painted a layer (11) of a first polymerisable material, the said first polymerisable material being of a type which, once polymerised, can form a layer which is impervious to any gaseous substance and which is completely polymerisable by heating to a first predetermined temperature;heating the element (1), with the said surface (2) to be painted covered with the said layer of first polymerisable material, to the said first predetermined temperature until the said first polymerisable material is completely polymerised to form a gas-impermeable layer (11) which covers the said surface to be painted completely;applying to the said surface (2) at least a base layer (12) of a predetermined thickness of a polymerisable electroconductive material, which is polymerisable by heating to a second predetermined temperature;heating the element (1) to the said second predetermined temperature to cause the polymerisation of the said base layer (12) of polymerisable electroconductive material, in such a way that the said base layer (12) of polymerisable electroconductive material is deposited not directly on the said surface (2) to be painted, but onto the said gas-impermeable layer (11);applying at least one layer of paint (13, 14) on top of the said base layer (12) of electroconductive polymerisable material;
- A method according to Claim 1 in which the said element (1) to be painted is formed from a material based on thermosetting vinyl ester/polyester resins, characterised in that the said second polymerisable material is constituted by a catalysed two-component polyurethane transparent paint.
- A method according to Claim 2, characterised in that the said first polymerisable material is applied on top of the said surface (2) to be painted to form thereon a layer (11) of between 30 and 40 microns thick.
- A method according to Claim 2 or Claim 3, characterised in that a layer (10) of adhesion promoter for the said first polymerisable material is applied in direct contact with the said surface (2) to be painted; this first polymerisable material being applied immediately on top of the said layer (10) formed from the adhesion promoter.
- A method according to Claim 4, characterised in that a polyester-based adhesion promoter ("Barrier") is used, applied to the said surface (2) to be painted in a continuous layer (10) at least 30 microns thick; and in that the said catalysed two-component polyurethane paint is chosen such that it is completely polymerised at a temperature of 60°C.
- A method according to Claim 5, characterised in that the said second two-component polyurethane paint is delivered to the said surface (2) by a "wet on wet" technique.
- A method according to any one of Claims 2 to 6, characterised in that the said electroconductive polymerisable material is a single-component primer which is polymerisable by heating to a temperature of at least 140-150°C.
- A painted element (1) formed from a synthetic plastics material, in particular a vehicle body part formed from a composite material, comprising a panel (1) pressed from at least one synthetic plastics resin, at least one visible surface (2) of which is covered by a plurality of layers of polymerisable materials including at least one layer of paint (13, 14); the said plurality of layers of polymerisable materials comprising, in order starting with the layer adjacent the said surface (2), a first, gas-impermeable layer (11), and a second, gas-permeable layer (12), both formed from respective different polymerised materials; the material forming the first layer (11) having a chemical composition such that it polymerises completely on heating to a first predetermined temperature; the material forming the second layer (12) having a chemical composition such that it forms an electroconductive primer for receiving the said at least one layer of paint (13, 14), and which polymerises on heating to a second predetermined temperature which is substantially equal to that needed to polymerise the at least one layer of paint;
the element being characterised in that the material forming the first layer (11) has been selected in such a way that said first predetermined temperature is below both the said second predetermined temperature and the lowest temperature of vaporisation of the monomers forming the said synthetic plastics resin from which the said panel is formed. - A painted element according to Claim 8, characterised in that the said panel (1) is formed from at least one thermosetting vinyl ester/polyester-based resin; and in that the first layer (11) is formed from a two-component polyurethane paint; the said first layer (11) being between 30 and 40 microns thick and being applied over a layer (10) of a material formed from a polyester-based adhesion promoter which is at least 30 microns thick applied directly to the said surface (2) provided with the layer (11) of paint.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT95TO000574A IT1276480B1 (en) | 1995-07-07 | 1995-07-07 | IMPROVED PAINTING METHOD APPLICABLE ON ELEMENTS MADE OF PLASTIC MATERIAL, PARTICULARLY AUTOMOTIVE COMPONENTS |
ITTO950574 | 1995-07-07 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0753358A1 EP0753358A1 (en) | 1997-01-15 |
EP0753358B1 true EP0753358B1 (en) | 2003-03-12 |
Family
ID=11413710
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP96110839A Expired - Lifetime EP0753358B1 (en) | 1995-07-07 | 1996-07-04 | Method of painting elements made from plastics, and elements formed thereby |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0753358B1 (en) |
DE (1) | DE69626575T2 (en) |
ES (1) | ES2191726T3 (en) |
IT (1) | IT1276480B1 (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19920799A1 (en) * | 1999-05-06 | 2000-11-16 | Basf Coatings Ag | Coating material curable thermally and with actinic radiation and its use |
DE19924674C2 (en) | 1999-05-29 | 2001-06-28 | Basf Coatings Ag | Coating material curable thermally and with actinic radiation and its use |
US6835759B2 (en) | 2001-08-28 | 2004-12-28 | Basf Corporation | Dual cure coating composition and processes for using the same |
US6852771B2 (en) | 2001-08-28 | 2005-02-08 | Basf Corporation | Dual radiation/thermal cured coating composition |
US6875471B2 (en) * | 2002-04-30 | 2005-04-05 | General Motors Corporation | Metallization of polymer parts for painting |
DE10347598A1 (en) * | 2003-10-14 | 2005-06-23 | Bayerische Motoren Werke Ag | Component, in particular outer skin component for a vehicle |
FR2980487B1 (en) * | 2011-09-23 | 2014-09-05 | Snecma | TURBOMACHINE PIECE, SUCH AS A TURBO AIRBORNE OR TURBOPROPULSER |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
UST982004I4 (en) * | 1974-12-23 | 1979-05-01 | Powder coated resinous article | |
FR2695048B1 (en) * | 1992-09-02 | 1994-10-14 | Manducher Sa | Process for the preparation of molded parts surfaces to be covered with electrostatic paint. |
CA2148885A1 (en) * | 1994-07-20 | 1996-01-21 | Frank Stubbs | Conductive color-keyed automotive primers |
-
1995
- 1995-07-07 IT IT95TO000574A patent/IT1276480B1/en active IP Right Grant
-
1996
- 1996-07-04 DE DE69626575T patent/DE69626575T2/en not_active Expired - Fee Related
- 1996-07-04 EP EP96110839A patent/EP0753358B1/en not_active Expired - Lifetime
- 1996-07-04 ES ES96110839T patent/ES2191726T3/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
ES2191726T3 (en) | 2003-09-16 |
DE69626575T2 (en) | 2004-04-08 |
ITTO950574A0 (en) | 1995-07-07 |
DE69626575D1 (en) | 2003-04-17 |
IT1276480B1 (en) | 1997-10-31 |
EP0753358A1 (en) | 1997-01-15 |
ITTO950574A1 (en) | 1997-01-07 |
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