POLYMER-BASED SUBSTRATE AND METHOD FOR PRODUCING THE SAME
20200290084 · 2020-09-17
Inventors
Cpc classification
C08L77/02
CHEMISTRY; METALLURGY
C08J2477/02
CHEMISTRY; METALLURGY
C09D177/02
CHEMISTRY; METALLURGY
C09D177/10
CHEMISTRY; METALLURGY
B05D7/02
PERFORMING OPERATIONS; TRANSPORTING
B05D3/005
PERFORMING OPERATIONS; TRANSPORTING
C08L77/06
CHEMISTRY; METALLURGY
C08J2477/06
CHEMISTRY; METALLURGY
C09D177/02
CHEMISTRY; METALLURGY
C08L77/06
CHEMISTRY; METALLURGY
B05D5/06
PERFORMING OPERATIONS; TRANSPORTING
C08J2479/08
CHEMISTRY; METALLURGY
C08J7/0427
CHEMISTRY; METALLURGY
C09D177/06
CHEMISTRY; METALLURGY
C08J7/043
CHEMISTRY; METALLURGY
C08L77/02
CHEMISTRY; METALLURGY
B05D1/04
PERFORMING OPERATIONS; TRANSPORTING
C08J2379/08
CHEMISTRY; METALLURGY
C08J7/044
CHEMISTRY; METALLURGY
Y02P20/582
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
C08J2377/06
CHEMISTRY; METALLURGY
International classification
B05D7/02
PERFORMING OPERATIONS; TRANSPORTING
C09D177/06
CHEMISTRY; METALLURGY
C09D177/02
CHEMISTRY; METALLURGY
C09D177/10
CHEMISTRY; METALLURGY
B05D3/00
PERFORMING OPERATIONS; TRANSPORTING
Abstract
A polymer-based substrate is proposed, which in particular is electrostatically coatable, wherein the substrate comprises a substrate base body made using a polymeric material and a coating applied to a surface region of the substrate base body, wherein the polymeric material comprises a first polymer, wherein the coating comprises a matrix polymer and an additive which is dispersed in the matrix polymer and reduces the surface resistance of the coating, said additive having a proportion that is selected such that the specific surface resistance of the coating is about 10.sup.10 Ohm or less, and wherein the matrix polymer is selected such that it is compatible with the first polymer.
Claims
1. A polymer-based substrate, comprising a substrate base body made using a polymeric material and a coating applied to a surface region of the substrate base body, wherein the polymeric material comprises a first polymer, wherein the coating comprises a matrix polymer and an additive which is dispersed in the matrix polymer and reduces the surface resistance of the coating, said additive having a proportion that is selected such that the specific surface resistance of the coating is about 10.sup.10 Ohm or less, and wherein the matrix polymer is selected such that it is compatible with the first polymer.
2. The substrate in accordance with claim 1, wherein the specific surface resistance of the layer with a reduced specific surface resistance is about 10.sup.9 Ohm or less.
3. The substrate in accordance with claim 1, wherein the matrix polymer is selected such that it is molecularly or microscopically mixable with the first polymer.
4. The substrate in accordance with claim 1, wherein the first polymer and the matrix polymer are soluble or swellable in the same solvent.
5. The substrate in accordance with claim 1, wherein the first polymer and the matrix polymer are selected from the polymer groups polyamide, polyester, polyether, polyketone, polyvinyl, poly-olefin and copolymers and functionalized polymers thereof.
6. The substrate in accordance with claim 1, wherein the first polymer and/or the matrix polymer is/are selected from the polymer group of polyamides.
7. The substrate in accordance with claim 1, wherein the first polymer in the polymeric material is present as a blend with a second polymer.
8. The substrate in accordance with claim 1, wherein the polymeric material comprises reinforcing substances.
9. The substrate in accordance with claim 1, wherein the additive for reducing the surface resistance of the coating is selected from the carbon-based components conductive soot, carbon nanotubes (CNT), carbon fibers, carbon layered materials, electrically conductive organic compounds, conductive polymers, electrically conductive ceramic, metal powders and metal fibers.
10. The substrate in accordance with claim 1, wherein the coating has an average thickness of about 100 m or less.
11. The substrate in accordance with claim 1, wherein the coating is configured as a continuous or large-area coating.
12. The substrate in accordance with claim 1, wherein the coating is selectively applied to one or a plurality of predetermined surface region(s) of the substrate body which is/are provided for a subsequent electrostatic coating, or which extends/extend substantially in parallel to a surface region of the substrate which is provided for an electrostatic coating.
13. The substrate in accordance with claim 1, wherein the substrate is configured as a heat-insulating profile, for the production of window, door, roof, or facade elements.
14. The substrate in accordance with claim 1, wherein the substrate is designed as a moulded part for an application outdoors.
15. The substrate in accordance with claim 1, wherein the matrix polymer has a temperature stability of about 200 C. or more.
16. The substrate in accordance with claim 1, wherein the coating is UV-stable.
17. The substrate in accordance with claim 1, wherein the substrate has a powder lacquer layer.
18. The substrate in accordance with claim 17, wherein the lacquer layer on the coating in the lacquered region has a lacquer coverage rate of about 90% or more.
19. A method for producing an electrostatically lacquerable, polymer-based substrate, wherein the method comprises: providing a substrate base body made using a polymeric material, wherein the polymeric material comprises a first polymer, providing a coating composition, comprising a solvent, a matrix polymer dissolved in the solvent, and an additive reducing the electrical resistance, wherein the solvent is selected such that the first polymer is soluble or swellable in the solvent, wherein the matrix polymer is compatible with the first polymer, and wherein the additive is dispersed in the coating composition, applying the coating composition to a surface region of the sub-strate base body while forming a surface layer, and removing the solvent from the surface layer.
20. The method in accordance with claim 19, wherein the solvent is selected such that the first polymer has a solubility of about 10% by weight or more.
21. The method in accordance with claim 19, wherein the solvent is selected such that the first polymer is swellable in the solvent.
22. The method in accordance with claim 19, wherein the solvent is selected from volatile solvents and has a boiling point or decomposition point of about 210 C. or less.
23. The method in accordance with claim 19, wherein the first polymer is selected from polyamide, polyester, polyether, polyketone, polyolefin, polyvinyl, and copolymers and functionalized polymers thereof; wherein the matrix polymer is selected from polyamide, polyester, polyether, polyketone, polyolefin, and polyvinyl; wherein the solvent comprises an organic liquid, selected from an aromatic hydrocarbon and/or carboxylated hydrocarbons, or a mineral acid and mixtures thereof and/or aqueous solutions thereof; and wherein the electrical resistance-reducing additive is substantially uniformly distributed in the matrix polymer.
24. The method in accordance with claim 19, wherein a surface region of the substrate is electrostatically powder lacquered with a lacquer powder after the application of the coating, wherein the powder lacquer is baked at a temperature of about 170 C. or more.
25. The method in accordance with claim 24, wherein the lacquer layer on the coating in the lacquered region has a lacquer coverage rate of about 90% or more.
26. The substrate in accordance with claim 4, wherein the solvent is a pure substance or a mixture of a plurality of pure substances, wherein the pure substance or the pure substances are selected from the organic liquids, aromatic hydrocarbons, esters, ethers, ketones, carboxylated hydrocarbons or inorganic acids.
27. The substrate in accordance with claim 6, wherein a) the first polymer is a polyamide 66, a polyamide 6, or a partially aromatic polyamide, and/or b) the matrix polymer is a polyamide 6, a polyamide 66, a polyamide 610, or a polyamide 410.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0137] In the drawings:
[0138]
[0139]
[0140]
[0141]
[0142]
[0143]
[0144]
[0145]
DETAILED DESCRIPTION OF THE DRAWINGS
[0146]
[0147] The cross section has on both sides of a planar middle section 12 offset regions 14, 16, the free rims of which are configured as so-called roll-in projections 18, 20. The roll-in projections can be guided into corresponding recesses of metal profiles and be connected to the metal profile in a shear-resistant manner by means of a so-called roll-in process.
[0148] The substrate base body 10 is typically made of a polymeric material, for example based on polyamide as the first polymer.
[0149]
[0150] The process of applying the coating is implemented here with spray technique, symbolized by a spray 24 which is applied in the direction of the arrow a to the surface of the insulating profile 10 located on top (viewing side 28) in
[0151] The surface layer may be applied, for example, as a dispersion of conductive soot in a solution of polyamide 6 (PA6) in methane acid.
[0152] It can be seen in
[0153] In
[0154] This substrate shape shown in
[0155] In
[0156] In
[0157] The substrate 42 (insulating profile) in accordance with the invention has on its upper surface which is accessible here from the outside, in accordance with the invention, a coating 56 which extends, analogously to
[0158] When rolling the roll-in profiles 48, 50 into the roll-in grooves 52, 54 of the metal parts 44, 46, a conductive contact with the coating 56 is produced, such that an electrostatic powder coating of a particularly high quality can be applied here.
[0159] The situation after the powder lacquering of the dry substrates is depicted in
[0160] The electrostatically applied lacquer layer 60 is in particular very uniform and free of bubbles and has a high lacquer coverage rate.
[0161]
[0162] In contrast to the depiction of
[0163] A powder lacquer layer 90 is again applied here on the viewing side. Said layer extends again from the face side of the first metal profile 74 over to the insulating profile 72 to the face side of the second metal profile 76. By means of the coating 86 with a reduced specific surface resistance of 10.sup.10 Ohm or less, applied in accordance with the invention to the substrate base body, the prerequisite is again met so that a continuous, flawless lacquer layer 90, which abuts directly against the substrate base body 73 in the region between the metal profiles 74, 76, can be applied to the viewing side of the composite profile 72.
[0164]
[0165] The substrate base body 100 has, in addition to a middle planar section 102, laterally adjoining offset regions 104, 106, which are then each adjoined by so-called roll-in projections 108 and 110, respectively.
[0166] The substrate base body 100 of
[0167] In
[0168] In
[0169] In a further variant, shown in
[0170] Another variant of the selective coating of the substrate base body 100 is shown in
[0171] In the sixth example of
[0172] In each of the embodiments of
[0173] In the other embodiments of
[0174] In
[0175] In
[0176] The lettering ABC 123 .circle-solid. serves only as an example of any labeling that could be applied in this way to the surface of the middle section 152, optionally also on other surface regions of a substrate base body 150, by means of the coating in accordance with the invention. Typically, e.g., suitable printer systems, stamps, or stencils are used for this purpose.
[0177] In
[0178] Here, too, there is the possibility of electrical dissipation via metal profiles (not shown) in the rolled-in state of the substrate base body 150 in an electrostatic powder lacquering.
[0179] In
[0180] Finally, in
[0181] Because the coating region 168b extends transversely over all strip-shaped sections of the pattern 168a, a dissipating function can again be ensured when the base body 150 is present with metal profiles in the roll-in composite.
[0182] In
[0183] The cross-cut test was performed on this sample.
[0184] Shown in the illustrations of
[0185]
[0186]
[0187] In the left region 208 of the substrate 206, before the powder application the substrate base body was equipped in accordance with the invention with a coating according to Example 7 described in the following, as is shown roughly in the case of the insulating profile of
[0188] The powder application to the present composite sample took place in one operation on the dried composite profile. There are very considerable differences in the lacquer coverage rate, which in the region 208 is nearly 100% and in the region 210 lacquer deposition is hardly visible to the naked eye.
EXAMPLES
[0189] In the following examples the specific surface resistance was determined on substrate base bodies (reference examples 1 to 3) and on substrates in accordance with the invention (examples 4 to 6) after storage in a standard climate and after an additional drying.
[0190] In each case extruded insulating profiles were used as substrate base bodies, the measurement of the specific surface resistance was performed on the so-called viewing side 28 of the section 12 of the substrate base body 10 and on the surface of the coating 32, respectively.
Example 1 (Reference)
[0191] In this example a solid, extruded insulating profile 10 with a planar middle section similar to the one in
[0192] A planar test piece is then milled from the profile, which is suitable for the measurement of the specific surface resistance.
[0193] The measured values for the specific surface resistance, measured under various conditions, are displayed in Table 1.
Example 2 (Reference)
[0194] In this example, again a solid, extruded insulating profile 10 with a planar middle section 10 similar to the one depicted in
[0195] A planar test piece is then milled from the profile, which is suitable for measuring the specific surface resistance.
[0196] The measured values for the specific surface resistance, measured under various conditions, are displayed in Table 1. Due to the higher proportion of glass fibers, it results in a slightly higher specific surface resistance in comparison to the measured values of Example 1.
Example 3 (Reference)
[0197] In this example, again a solid, extruded insulating profile 10 with a planar middle section similar to the one depicted in
[0198] The measured values for the specific surface resistance, measured under various conditions, are displayed in Table 1. Due to the different composition (no PPE fraction) of the polymeric material, in particular the thereby higher proportion of (moisture-absorbing) PA66, there is a further reduced specific surface resistance in comparison to the measured values in Examples 1 and 2.
[0199] The lacquer coverage rate of the dried and powder lacquered profile is only about 56% and is thus obviously insufficient. The lacquering tests were performed with a white powder lacquer of the type SA816G Interpon D1036 (manufacturer: Akzo Nobel Powder Coatings GmbH). For this purpose, the powder lacquer was applied to the pre-dried substrate using a commercially available powder gun for electrostatic powder coating and was baked in an oven at 200 C. for 20 minutes.
Example 4
[0200] In this example again an insulating profile 10, as described in (reference) Example 1, is used as a substrate base body.
[0201] In contrast to Example 1, the insulating profile 10 has now been provided, in accordance with the invention, with a coating 32, as can be seen in
[0202] A coating composition containing conductive soot was produced as the coating mass for producing the coating 32. For this purpose, a commercially available conductive soot concentrate of the type Hubron NBB310 (manufacturer: Hubron International, Great Britain) in concentrated methane acid (concentration >98%, Carl Roth GmbH+Co. KG) with a solids content of 50 g/l was introduced, dispersed, and applied to the surface of the substrate base body by means of spray coating. The conductive soot concentrate Hubron NBB310 is, according to the manufacturer's information, conductive soot in a matrix polymer of PA6 with small amounts of an unspecified ethylene terpolymer as a modifier.
[0203] The PA6 mass with conductive soot was dissolved under heavy stirring upon introduction into the methane acid and was subsequently further dispersed using a rotor-stator mixer (Ultra-Turrax of the company IKA) to finely distribute the conductive soot in the PA6 methane acid solution. This coating composition is used in a timely manner in order to avoid degradation or sedimentation.
[0204] Alternatively, of course other dispersion techniques can be used like, for example, grinding in ball mills, wet mills, colloid mills, or by means of high-pressure homogenizers, rolling mills and ultrasonic homogenizers. This process can finally be supplemented by pressing through fine nozzles, decanting, filtering, or otherwise fractioning one or more times in order to remove poorly dispersed coarse fractions of the conductive soot.
[0205] The spraying of the coating composition onto the substrate base body is carried out by means of a pressurized air-operated lacquer spray gun with a flat jet nozzle (nozzle diameter 1.5 mm), wherein the substrate base body is continuously moved through the fine mist, such that a thin but deep black and opaque application is obtained without large amounts of the liquid coating composition accumulating.
[0206] The drying is carried out by airing the substrates at room temperature with good ventilation, this being completed in a time of about 0.5 to 1 minute and the substrates then being hand-dry and matte black.
[0207] The average layer thickness of the coating 32 was about 1 m to about 5 m.
[0208] The measured values for the specific surface resistance of the coating 32, measured under different conditions, are displayed in Table 1. In comparison to the measured values of Examples 1 to 3, there is a significantly reduced specific surface resistance due to the proportion of additive (conductive soot). The effect of the drying process on the measured specific surface resistance is lower (as a percentage) here than in the reference examples 1 to 3.
Example 5
[0209] In this example again an insulating profile 10, described as described in Example 2, is used as a substrate base body.
[0210] In contrast to Example 2, the insulating profile 10 has now been provided, in accordance with the invention, with a coating 32, as can be seen in
[0211] The coating 32 way produced from a composition in accordance with Example 4.
[0212] The spraying of the coating composition onto the substrate and the drying takes place analogously to Example 4.
[0213] The average layer thickness of the coating 32 was about 1 m to about 5 m.
[0214] The measured values for the specific surface resistance of the coating 32, measured under different conditions, are displayed in Table 1. In comparison to the measured values of Examples 1 to 3, there is a significantly reduced specific surface resistance due to the proportion of additive (conductive soot). The effect of the drying process on the measured specific surface resistance is lower (as a percentage) here, too, than in the reference Examples 1 to 3.
Example 6
[0215] In this example again an insulating profile 10, described as described in Example 3, is used as a substrate base body.
[0216] In contrast to Example 3, the insulating profile 10 has now been provided, in accordance with the invention, with a coating 32, as can be seen in
[0217] The coating 32 was obtained from a coating composition in accordance with the description in Example 4.
[0218] The spraying of the coating composition onto the substrate and the drying again take place analogously to Example 4.
[0219] The average layer thickness of the coating 32 was about 1 m to about 5 m.
[0220] The measured values for the specific surface resistance of the coating 32, measured under different conditions, are displayed in Table 1. The effect of the drying process on the measured specific surface resistance is lower (as a percentage) here than in the reference Examples 1 to 3.
[0221] The lacquer coverage rate of the dried and powder lacquered profile is about 100% and is thus perfect. The lacquering tests were performed analogously to Example 3 and again with a white powder lacquer of the type SA816G Interpon D1036 (manufacturer: Akzo Nobel Powder Coatings GmbH). For this purpose, the powder lacquer was applied to the pre-dried substrate using a commercially available powder gun for electrostatic powder coating and was baked in an oven at 200 C. for 20 minutes.
[0222] Examples 1 to 6 hereby clearly show that the specific surface resistance can already be significantly reduced by applying a thin coating in according to the invention and thus can result in electrical conductivity of the surface. An adaptation of the surface resistance, if desired, is easily possible by adapting the formulation, for example by changing the proportion of the conductive additive.
Example 7
[0223] An insulating profile 30, produced in accordance with the invention, with the coating 32 was processed to a metal-plastic profile (analogously to
[0224] A bone-shaped in insulating profile of the type insulbar L018 from the company Ensinger GmbH, which was coated in accordance with the invention with a dispersion of Hubron NBB310 in methane acid (solids content 50 g/L), serves here as a base.
[0225] The production of the coating composition and the implementation of the spraying of the coating composition correspond to the description in Example 4. The average layer thickness of the coating 32 was about 1 m to 5 m.
[0226] To be able to compare the positive effects on the substrate in accordance with the invention directly with the untreated substrate base body, for test purposes rectangular regions of the substrate base bodies were covered and as a result were not provided with the coating in segments. One thus obtains test samples in the form of substrates (insulating profiles) which have a direct sequence of regions or segments that take well and take poorly to being coated (see
[0227] The lacquering tests were performed with a white powder lacquer of the type SA816G Interpon D1036 (manufacturer: Akzo Nobel Powder Coatings GmbH). The powder lacquer was applied to the pre-dried substrates (<0.1% by weight residual moisture) using a commercially available powder gun for electrostatic powder coating and was baked in an oven at 200 C. for 20 minutes.
[0228] While no continuously covering lacquer layer could be formed on the reference example, i.e., the profile segment 210 without a coating in accordance with the invention (lacquer coverage not visible to the naked eye, thus completely inadequate), the powder lacquering of the substrate 206 in accordance with the invention in the region 208 resulted in a visually appealing, continuous, uniform white lacquer layer with very good lacquer adhesion to the coating 32 in accordance with the invention.
[0229] The lacquer adhesion to the substrate in the region 208 was tested using a cross-cut test (DIN EN ISO 2409), the result of which is shown in
Example 8
[0230] In order to evaluate the possible change in the mechanical properties of the substrates 30 due to contact with a good solvent for the first polymerin this case methane acidmechanical test were performed on uncoated substrate base bodies 10 of the type insulbar REG in accordance with Example 3 and on substrates coated in accordance with the invention according to Example 6each without a powder lacquering having been performed.
[0231] Mechanical tests were hereby performed in the form of tensile tests, each with a set of n=10 test pieces; these were milled from the insulating profiles used. For evaluating the parameters E-modulus, transversal and longitudinal tensile strength (in relation to the longitudinal direction of the profiles) and the elongation at break, in each case the arithmetic mean was established.
[0232] For Example 8a, an untreated substrate base body 10 of the type insulbar REG as described in Example 7 is used as a reference. Example 8b corresponds to the substrate coated in accordance with the invention (insulating profile 30 with the coating 32) in Example 6. The results are summarized in Table 2 and show that the application of a coating 32 does not significantly influence the observed mechanical parameters of the substrate base body.
TABLE-US-00001 TABLE 1 realized layer thicknesses of the coatings in Examples 4 to 6 are on average about 1 m to about 5 m. Specific surface re- Specific sistance surface (storage resistance in a after Conduc- Material standard drying Ex- First Matrix tive substrate climate) (160 C./ ample polymer polymer additive base body Coating [] 6 h) [] 1 PA66 without without blend of PA66 with uncoatedreference 5.69E+13 6.63E+14 PPE and 10% GF 2 PA66 without without blend of PA66 with uncoatedreference 1.49E+14 7.20E+14 PPE and 20% GF 3 PA66 without Without PA66 25% GF uncoatedreference 4.50E+13 2.73E+14 4 PA66 PA6 conductive blend of PA66 with spray coating with disper- 7.79E+05 1.13E+06 soot PPE and 10% GF sion of conductive soot- PA6 compound in formic acid (solids content 50 g/L) 5 PA66 PA6 conductive blend of PA66 with spray coating with disper- 5.12E+05 7.73E+05 soot PPE and 20% GF sion of conductive soot- PA6 compound in formic acid (solids content 50 g/L) 6 PA66 PA6 conductive PA66 25% GF spray coating with disper- 1.7E+05 2.02E+05 soot sion of conductive soot- PA6 compound in formic acid (solids content 50 g/L)
TABLE-US-00002 TABLE 2 change in selected mechanical properties of substrate base bodies after the application of a coating in accordance with the invention Elon- gation Tensile Tensile Residual Substrate E- at strength, strength, moisture Ex- base modulus break longitudinal transversal [% by ample body Coating [relative] [relative] [relative] [relative] weight 8a-ref. insulbar REG without 100.0% 100.0% 100.0% 100.0% 0.3 8b insulbar REG with 100.5% 102.4% 100.1% 99.3% 0.3