CA2066149A1 - Method for coating a fibre-reinforced plastics body - Google Patents
Method for coating a fibre-reinforced plastics bodyInfo
- Publication number
- CA2066149A1 CA2066149A1 CA002066149A CA2066149A CA2066149A1 CA 2066149 A1 CA2066149 A1 CA 2066149A1 CA 002066149 A CA002066149 A CA 002066149A CA 2066149 A CA2066149 A CA 2066149A CA 2066149 A1 CA2066149 A1 CA 2066149A1
- Authority
- CA
- Canada
- Prior art keywords
- particles
- layer
- synthetic resin
- resistant coating
- spraying
- 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.)
- Abandoned
Links
- 238000000034 method Methods 0.000 title claims abstract description 63
- 238000000576 coating method Methods 0.000 title claims abstract description 37
- 239000011248 coating agent Substances 0.000 title claims abstract description 32
- 229920002430 Fibre-reinforced plastic Polymers 0.000 title abstract description 10
- 239000011151 fibre-reinforced plastic Substances 0.000 title abstract description 10
- 239000002245 particle Substances 0.000 claims abstract description 70
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 65
- 239000000057 synthetic resin Substances 0.000 claims abstract description 65
- 239000000463 material Substances 0.000 claims abstract description 40
- 229910052751 metal Inorganic materials 0.000 claims abstract description 21
- 239000002184 metal Substances 0.000 claims abstract description 21
- 238000007751 thermal spraying Methods 0.000 claims abstract description 15
- 239000011159 matrix material Substances 0.000 claims abstract description 13
- 230000003014 reinforcing effect Effects 0.000 claims abstract description 9
- 239000000919 ceramic Substances 0.000 claims abstract description 3
- 239000010410 layer Substances 0.000 claims description 111
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 18
- 239000000956 alloy Substances 0.000 claims description 17
- 229910045601 alloy Inorganic materials 0.000 claims description 17
- 229920005989 resin Polymers 0.000 claims description 14
- 239000011347 resin Substances 0.000 claims description 14
- 239000000126 substance Substances 0.000 claims description 14
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 12
- 238000004519 manufacturing process Methods 0.000 claims description 11
- 239000004033 plastic Substances 0.000 claims description 11
- 229920003023 plastic Polymers 0.000 claims description 11
- 239000011247 coating layer Substances 0.000 claims description 10
- 238000010285 flame spraying Methods 0.000 claims description 10
- 150000002739 metals Chemical class 0.000 claims description 10
- 229920001568 phenolic resin Polymers 0.000 claims description 10
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 9
- 229910052799 carbon Inorganic materials 0.000 claims description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 8
- 238000005299 abrasion Methods 0.000 claims description 8
- 239000002131 composite material Substances 0.000 claims description 8
- 229910052759 nickel Inorganic materials 0.000 claims description 8
- 238000005507 spraying Methods 0.000 claims description 7
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 6
- 238000004873 anchoring Methods 0.000 claims description 6
- 229910052804 chromium Inorganic materials 0.000 claims description 6
- 239000011651 chromium Substances 0.000 claims description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 5
- 238000007750 plasma spraying Methods 0.000 claims description 5
- 229910052710 silicon Inorganic materials 0.000 claims description 5
- 239000010703 silicon Substances 0.000 claims description 5
- 239000004411 aluminium Substances 0.000 claims description 4
- 229910052782 aluminium Inorganic materials 0.000 claims description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 4
- 229910052742 iron Inorganic materials 0.000 claims description 4
- 235000012239 silicon dioxide Nutrition 0.000 claims description 4
- 239000004753 textile Substances 0.000 claims description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- 229910017052 cobalt Inorganic materials 0.000 claims description 3
- 239000010941 cobalt Substances 0.000 claims description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 3
- 229910052802 copper Inorganic materials 0.000 claims description 3
- 239000010949 copper Substances 0.000 claims description 3
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 3
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims description 3
- 239000000377 silicon dioxide Substances 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- 229910052720 vanadium Inorganic materials 0.000 claims description 3
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims description 3
- 229910010293 ceramic material Inorganic materials 0.000 claims description 2
- 238000000151 deposition Methods 0.000 claims description 2
- 239000007769 metal material Substances 0.000 claims description 2
- 239000007921 spray Substances 0.000 claims description 2
- 239000004408 titanium dioxide Substances 0.000 claims description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims 2
- 229910010271 silicon carbide Inorganic materials 0.000 claims 2
- 229910001928 zirconium oxide Inorganic materials 0.000 claims 2
- 229910000838 Al alloy Inorganic materials 0.000 claims 1
- 229910000881 Cu alloy Inorganic materials 0.000 claims 1
- 239000012790 adhesive layer Substances 0.000 claims 1
- VXAUWWUXCIMFIM-UHFFFAOYSA-M aluminum;oxygen(2-);hydroxide Chemical compound [OH-].[O-2].[Al+3] VXAUWWUXCIMFIM-UHFFFAOYSA-M 0.000 claims 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims 1
- 239000002585 base Substances 0.000 description 14
- 239000000843 powder Substances 0.000 description 14
- 239000004744 fabric Substances 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- 238000000227 grinding Methods 0.000 description 7
- 239000000543 intermediate Substances 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000000835 fiber Substances 0.000 description 5
- 238000005755 formation reaction Methods 0.000 description 5
- 238000004804 winding Methods 0.000 description 5
- 229920001342 Bakelite® Polymers 0.000 description 4
- 239000004637 bakelite Substances 0.000 description 4
- 239000000428 dust Substances 0.000 description 4
- 239000003822 epoxy resin Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 239000011888 foil Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 229920000647 polyepoxide Polymers 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 238000007605 air drying Methods 0.000 description 3
- 239000007767 bonding agent Substances 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 238000003754 machining Methods 0.000 description 3
- 239000000123 paper Substances 0.000 description 3
- 238000007639 printing Methods 0.000 description 3
- 239000011241 protective layer Substances 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 238000007514 turning Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 230000032798 delamination Effects 0.000 description 2
- 229910003460 diamond Inorganic materials 0.000 description 2
- 239000010432 diamond Substances 0.000 description 2
- -1 for example Polymers 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 238000011089 mechanical engineering Methods 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 230000003746 surface roughness Effects 0.000 description 2
- 229920002748 Basalt fiber Polymers 0.000 description 1
- 229910000599 Cr alloy Inorganic materials 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 229910000990 Ni alloy Inorganic materials 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 241000206607 Porphyra umbilicalis Species 0.000 description 1
- 208000034809 Product contamination Diseases 0.000 description 1
- MCMNRKCIXSYSNV-UHFFFAOYSA-N ZrO2 Inorganic materials O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 238000003486 chemical etching Methods 0.000 description 1
- 239000000788 chromium alloy Substances 0.000 description 1
- 229940000425 combination drug Drugs 0.000 description 1
- 230000000875 corresponding effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000003116 impacting effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 238000010290 vacuum plasma spraying Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/043—Improving the adhesiveness of the coatings per se, e.g. forming primers
-
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C33/00—Moulds or cores; Details thereof or accessories therefor
- B29C33/56—Coatings, e.g. enameled or galvanised; Releasing, lubricating or separating agents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C70/00—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
- B29C70/02—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising combinations of reinforcements, e.g. non-specified reinforcements, fibrous reinforcing inserts and fillers, e.g. particulate fillers, incorporated in matrix material, forming one or more layers and with or without non-reinforced or non-filled layers
- B29C70/021—Combinations of fibrous reinforcement and non-fibrous material
- B29C70/025—Combinations of fibrous reinforcement and non-fibrous material with particular filler
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C70/00—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
- B29C70/58—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising fillers only, e.g. particles, powder, beads, flakes, spheres
- B29C70/64—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising fillers only, e.g. particles, powder, beads, flakes, spheres the filler influencing the surface characteristics of the material, e.g. by concentrating near the surface or by incorporating in the surface by force
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/04—Reinforcing macromolecular compounds with loose or coherent fibrous material
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/046—Forming abrasion-resistant coatings; Forming surface-hardening coatings
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/12—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the method of spraying
- C23C4/129—Flame spraying
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/12—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the method of spraying
- C23C4/134—Plasma spraying
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Composite Materials (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Materials Engineering (AREA)
- Plasma & Fusion (AREA)
- Physics & Mathematics (AREA)
- Metallurgy (AREA)
- Manufacturing & Machinery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Coating By Spraying Or Casting (AREA)
- Laminated Bodies (AREA)
- Reinforced Plastic Materials (AREA)
- Inking, Control Or Cleaning Of Printing Machines (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
Abstract
Abstract Method for coating a fibre-reinforced plastics body For the application of a firmly adhering resistant, metal or ceramics coating to bodies consisting of reinforcing fibres and a synthetic resin matrix by means of a thermal spraying process, there is introduced into the surface of the fibre-reinforced synthetic resin body facing the subsequently applied thermally sprayed layer, a material in particle form which is capable of combining chemically with the material serving as a thermal coating material. Before thermal spraying takes place, the surface of the body to be coated is removed in such a way that clean exposed surfaces of the dispersed particles result, enabling the bonding of the layers.
Description
~6~
25861-1~
The invention relates to a method for the application of at least one firmly-adhering resistant coating layer to a surface of a body made of a composite material of reinforcing fibres and a plastic matrix.
By the use of fibre-reinforced plastics, considerable advantages can be achieved in mechanical engineering, vehicle and plant construction as well as in the building industry.
Fibre-reinforced plastics are generally lighter than metals, have good corrosion resistance and, with an appropriate design, at least equally good mechanical properties in relation to weight.
These advantages are particularly evident in the case of rapidly moving parts such as, for example, shafts, cylinders, rollers, tappets, levers or propellers, etc.
Rapidly rotating rollers made of metals, for example for paper and foil manufacturing and processing or printing machines are, because of their heavy weight, subject to consider-able centrifugal forces, the inertial forces as well as motive forces are relatively great, and large demands are made on the weight balance. Nowadays, therefore, rollers used for this purpose are made of fibre-reinforced plastics, in particular carbon fibre-reinforced plastics, which have a substantially smaller weight than rollers made of metal, with the same rigidity and improved dimensional stability (DE-GM 83 22 639).
In plant construction and in tank construction, as well as in the building industry, it is advantageous to make use of the high leve] of tensile and bending strength, the outstanding torsional rigidity and the corrosion resistance of the reinforced 2 0 ~ 9 plastics materials, which are lighter in comparison with metals or ceramics materials.
When the surfaces of fibre-reinforced plastics are used for conveying or transporting operations, or when they are acted upon by substances which are in motion relative to these surfaces, however, they frequently prove to be too poorly resistant thereof.
For reducing abrasion phenomena and preventing product contamina-tion, it has therefore been proposed to coat the surfaces with a resistant metal by electrolytic deposition, (DE-GM 84 06 019).
The quality of layers applied in this way, however, is unsatisfactory in many cases because of insufficient adhesion.
According to another process (GB 887 366), moulded bodies made of hardenable plastics, such as formaldehyde resins, are provided by flame spraying with coatings made of metals or alloys which are intended to make these parts resistant to collision and impact stresses. This process is complicated and expensive according to the present state of the art. In addition, the adhesion of the layers is unsatisfactory for modern requirements, in particular when under dynamic stress, and the choice of materials which can be sprayed on and can be combined is limited. In order to obtain layers with sufficient adhesion, special requirements must in fact be observed. The material for the first layer cannot be freely selected. Its melting point must be 400C above the decomposition point of the plastics and its thermal expansion coefficient must be greater than that of the plastics. Further-more, it is required that the material from which the second layer is to be built up has a smaller expansion coefficient than the previously applied first layer, and this already indicates .
2 ~
25861-1~
poor adhesion of the first layer to its substrate. The plastics parts to be coated can contain fillers such as coke powder, graphite, wood dust, rock flour, quartz powder, paper or textile shreds, which are possibly to serve for lowering the thermal expansion coefEicient. Participation o this filler in the anchoring of the metals sprayed on to the plastics surface is not lndicated in the text, and is not possible because of the differences between the filler and the coating material.
Swiss Patent No. 538 549 also deals with the applica~
tion by flame spraying of protective layers to plastics parts produced from synthetic resin, fillers and/or fibres. According to this patent, protective layers can be applied according to the flame spraying process, but these layers have unsatisfactory adhesion, or irreparable damage occurs to the surface of the support substance. In particular, damage to the reinforcing fibres is caused by the method. In order to solve the problems, therefore, there is first applied to the fibre-reinforced basic body an intermediate layer made from a fabric or net and a synthetic resin, which layer serves as an adhesion primer and buffer during flame spraying. The sprayed-on particles penetrate between the individual fabric pores and thus achieve deep anchoring. This method is not technically satisfactory either and is also expensive, because the manufacture of the intermediate layer is only possible with substances which are available in fabric or net form; the processing of fabrics and braids requires expensive hand working or special technical apparatus and the fabric or braid must be matched precisely to the surface of the 2~61~9 base body, which causes problems, in particular in the case of closed surfaces, because of the occurrence of butt joints or overlapping. This fabric-containing layer serves as a thermal barrier during flame spraying. It is therefore subject to high internal stresses caused by differences in the thermal expansion coefficients between the synthetic resin matrix and the material of the fabric. These stresses can, with an outer sprayed-on layer which adheres quite well, lead to internal defects and delamination in the base body. However, the bonding of the sprayed-on layer also leaves something to be desired, in spite of improvements over the prior art since, during flame spraying, in all cases the hot particles first meet a synthetic resin surface which then decomposes to a greater or lesser extent and, as tests have since shown, prevents the direct chemical bonding of the sprayed material to appropriately chosen fabric or net material.
In German Patent No. DE 35 27 912, another method for coating carbon fibre-reinforced plastics bodies with metals is described. Good bonding of the protective layer is achieved with this method by using the plasma spraying method in combina-tion with a carbon fibre-reinforced substrate surface which is based on a phenol formaldehyde resin. This method has indeed entered into industrial practice, but the durability of layers produced according to this method is not completely satisfactory, either. In the case of large mechanical loads such as those occurring during cutting up, grinding to size, under an impacting load or even a long operating load, delamination of the coating still occurs.
_ 5 _ 2~ 6~
25861~18 Thus, in the invention it is attempted to provide an improved method of the type described above, in which method the choice of synthetic resin used as a matrix and the choice of the substance used for the coating are not sub]ect to restrictions, the manufacture of the composite body which is capable of coating and of the coated composite body is simple and low-cost, and layers having substantially improved adhesion can be produced.
According to the invention, the surface to be coated has an outer layer made of a synthetic resin in which particles are incorporated. The particles are made of a material corres-ponding, as material, to the material which serves as the resistant coatin~ layer or which is capable of bonding chemically with the material serving as the resistant coating layer. A
surface of the outer layer is removed to such an extent and in such a way that the particles which are integrated into the surface have clean exposed surfaces free from the synthetic resin and pointing in the direction of the later coating. The material for producing the resistant coating is sprayed on the thus-treated surface by means of a thermal spraying operation.
The following, interacting factors are essential to the invention:
l. A base body made of fibre-reinforced plastics is bonded to a layer of a synthetic resin containing particles. The synthetic resin used for this layer shows, on the one hand, good bonding to or into the resin matrix of the base body and, on the other hand, good ability to retain the particles which may be granular to powdery.
~ 6 - 2~6~
2. The surface of the particle-containing outer layer is removed, in the cured state, to the extent that the particles, first coated with a layer of synthetic resin when subject to manufacturing conditions, have clean, exposed, outwardly directed surfaces, but, on the other hand, remain Eirmly anchored to the synthetic resin matrix.
25861-1~
The invention relates to a method for the application of at least one firmly-adhering resistant coating layer to a surface of a body made of a composite material of reinforcing fibres and a plastic matrix.
By the use of fibre-reinforced plastics, considerable advantages can be achieved in mechanical engineering, vehicle and plant construction as well as in the building industry.
Fibre-reinforced plastics are generally lighter than metals, have good corrosion resistance and, with an appropriate design, at least equally good mechanical properties in relation to weight.
These advantages are particularly evident in the case of rapidly moving parts such as, for example, shafts, cylinders, rollers, tappets, levers or propellers, etc.
Rapidly rotating rollers made of metals, for example for paper and foil manufacturing and processing or printing machines are, because of their heavy weight, subject to consider-able centrifugal forces, the inertial forces as well as motive forces are relatively great, and large demands are made on the weight balance. Nowadays, therefore, rollers used for this purpose are made of fibre-reinforced plastics, in particular carbon fibre-reinforced plastics, which have a substantially smaller weight than rollers made of metal, with the same rigidity and improved dimensional stability (DE-GM 83 22 639).
In plant construction and in tank construction, as well as in the building industry, it is advantageous to make use of the high leve] of tensile and bending strength, the outstanding torsional rigidity and the corrosion resistance of the reinforced 2 0 ~ 9 plastics materials, which are lighter in comparison with metals or ceramics materials.
When the surfaces of fibre-reinforced plastics are used for conveying or transporting operations, or when they are acted upon by substances which are in motion relative to these surfaces, however, they frequently prove to be too poorly resistant thereof.
For reducing abrasion phenomena and preventing product contamina-tion, it has therefore been proposed to coat the surfaces with a resistant metal by electrolytic deposition, (DE-GM 84 06 019).
The quality of layers applied in this way, however, is unsatisfactory in many cases because of insufficient adhesion.
According to another process (GB 887 366), moulded bodies made of hardenable plastics, such as formaldehyde resins, are provided by flame spraying with coatings made of metals or alloys which are intended to make these parts resistant to collision and impact stresses. This process is complicated and expensive according to the present state of the art. In addition, the adhesion of the layers is unsatisfactory for modern requirements, in particular when under dynamic stress, and the choice of materials which can be sprayed on and can be combined is limited. In order to obtain layers with sufficient adhesion, special requirements must in fact be observed. The material for the first layer cannot be freely selected. Its melting point must be 400C above the decomposition point of the plastics and its thermal expansion coefficient must be greater than that of the plastics. Further-more, it is required that the material from which the second layer is to be built up has a smaller expansion coefficient than the previously applied first layer, and this already indicates .
2 ~
25861-1~
poor adhesion of the first layer to its substrate. The plastics parts to be coated can contain fillers such as coke powder, graphite, wood dust, rock flour, quartz powder, paper or textile shreds, which are possibly to serve for lowering the thermal expansion coefEicient. Participation o this filler in the anchoring of the metals sprayed on to the plastics surface is not lndicated in the text, and is not possible because of the differences between the filler and the coating material.
Swiss Patent No. 538 549 also deals with the applica~
tion by flame spraying of protective layers to plastics parts produced from synthetic resin, fillers and/or fibres. According to this patent, protective layers can be applied according to the flame spraying process, but these layers have unsatisfactory adhesion, or irreparable damage occurs to the surface of the support substance. In particular, damage to the reinforcing fibres is caused by the method. In order to solve the problems, therefore, there is first applied to the fibre-reinforced basic body an intermediate layer made from a fabric or net and a synthetic resin, which layer serves as an adhesion primer and buffer during flame spraying. The sprayed-on particles penetrate between the individual fabric pores and thus achieve deep anchoring. This method is not technically satisfactory either and is also expensive, because the manufacture of the intermediate layer is only possible with substances which are available in fabric or net form; the processing of fabrics and braids requires expensive hand working or special technical apparatus and the fabric or braid must be matched precisely to the surface of the 2~61~9 base body, which causes problems, in particular in the case of closed surfaces, because of the occurrence of butt joints or overlapping. This fabric-containing layer serves as a thermal barrier during flame spraying. It is therefore subject to high internal stresses caused by differences in the thermal expansion coefficients between the synthetic resin matrix and the material of the fabric. These stresses can, with an outer sprayed-on layer which adheres quite well, lead to internal defects and delamination in the base body. However, the bonding of the sprayed-on layer also leaves something to be desired, in spite of improvements over the prior art since, during flame spraying, in all cases the hot particles first meet a synthetic resin surface which then decomposes to a greater or lesser extent and, as tests have since shown, prevents the direct chemical bonding of the sprayed material to appropriately chosen fabric or net material.
In German Patent No. DE 35 27 912, another method for coating carbon fibre-reinforced plastics bodies with metals is described. Good bonding of the protective layer is achieved with this method by using the plasma spraying method in combina-tion with a carbon fibre-reinforced substrate surface which is based on a phenol formaldehyde resin. This method has indeed entered into industrial practice, but the durability of layers produced according to this method is not completely satisfactory, either. In the case of large mechanical loads such as those occurring during cutting up, grinding to size, under an impacting load or even a long operating load, delamination of the coating still occurs.
_ 5 _ 2~ 6~
25861~18 Thus, in the invention it is attempted to provide an improved method of the type described above, in which method the choice of synthetic resin used as a matrix and the choice of the substance used for the coating are not sub]ect to restrictions, the manufacture of the composite body which is capable of coating and of the coated composite body is simple and low-cost, and layers having substantially improved adhesion can be produced.
According to the invention, the surface to be coated has an outer layer made of a synthetic resin in which particles are incorporated. The particles are made of a material corres-ponding, as material, to the material which serves as the resistant coatin~ layer or which is capable of bonding chemically with the material serving as the resistant coating layer. A
surface of the outer layer is removed to such an extent and in such a way that the particles which are integrated into the surface have clean exposed surfaces free from the synthetic resin and pointing in the direction of the later coating. The material for producing the resistant coating is sprayed on the thus-treated surface by means of a thermal spraying operation.
The following, interacting factors are essential to the invention:
l. A base body made of fibre-reinforced plastics is bonded to a layer of a synthetic resin containing particles. The synthetic resin used for this layer shows, on the one hand, good bonding to or into the resin matrix of the base body and, on the other hand, good ability to retain the particles which may be granular to powdery.
~ 6 - 2~6~
2. The surface of the particle-containing outer layer is removed, in the cured state, to the extent that the particles, first coated with a layer of synthetic resin when subject to manufacturing conditions, have clean, exposed, outwardly directed surfaces, but, on the other hand, remain Eirmly anchored to the synthetic resin matrix.
3. The first layer applied to this surface by means of a thermal spraying process anchors itself to and into the exposed surface portions of the particles which, on their unexposed sides, are firmly retained in the synthetic resin matrix of the intermediate layer. This anchoring is produced by a chemical bonding of the sprayed-on particles to the substrate particles embedded in the resin matrix. The lack of a synthetic resin skin covering the particle surfaces is essential for the satisfactory formation of such a bond. Tests have shown that the bonding of the thermally sprayed-on layer is drastically worsened if the hot particles must first break through a synthetic resin skin before they reach the surfaces of the particles anchored in the synthetic resin layer, or if they hardly achieve only a mechanical hold in the synthetic resin layer. Products of thermal decomposition which are produced upon the impact of the hot, molten coating particles with a synthetic resin surface, are also an obstacle to bonding. In contrast to all previously known methods, anchoring of the thermally sprayed-on layer in the synthetic resin substrate is no longer necessary with the method according to the invention.
The base body made of fibre-reinforced plastics may have any shape suitable for the use of a thermal spraying method.
20~6~9 A group of preferred bodies are flat or curved areal moulded bodies such as plates, bowls, containers or pipelines or segments thereof. Another group of preferable bodies have at least partially closed surfaces such as pipes, rollers, cylinders, cones or truncated cones.
Any synthetic resins from which bodies of the shape described above can be manufactured with sufficient stability of shape and temperature can be used as the base material and matrix material for the reinforcing fibres. In particular, preferred are thermosetting resins such as phenol formaldehyde, epoxy or polyester resins. However, thermoplastic resins such as, for example, polypropylene, polyamide or polycarbonate are also suitable. Carbon fibres (with graphite ibres being included in this term), glass fibres and arylamide fibres are particularly preferred as the reinforcing fibres. Where useful, other fibres, for example mineral fibres such as basalt fibres or rock wool, metal fibres and carbide fibres such as SiC whiskers, can also be used. The fibres can be incorporated into the synthetic resin body as short-chopped fibres or staple fibres, in the form of woven cloth, nets, knitted fabrics or other textile formations of two-dimensional or three-dimensional kind, or as continuous filaments.
Serving to provide bonding for the layer to be sprayed on thermally are particles which are incorporated either:
1) directly into a layer adjacent to the outer surface of the fibre-reinforced base body or 2) in a layer applied to the outer surface of the fibre-reinforced base body and firmly bonded to this surface.
2~6~9 In the first case, the particles are worked in directly during the formation of the outermost layers. The particles in the dry state can be processed. The particles may also be provided with a bonding agent or suspended in a resin or in a resin solution. This can take place, for example, by the simultaneous spraying-on of the particles and a short-fibre-reinforced synthetic resin material, using separate spraying devices operating in coordinated manner, or by the spraying-on of the synthetic resin containing the particles in a suitable manner, or by sprinkling the dry particles during the formation of a body reinforced with filaments, for example during the winding process.
In the second case, there is produced in an advantageous manner a mixture made of a synthetic resin which can bond well to the base body made of fibre-reinforced synthetic resin, and the particles. The synthetic resin selected for this purpose may be the same as that of the base body or it may be another which is capable of bonding well to the base body, of retaining well the particles and of being well machined after curing. This mixture of the synthetic resin and the particles is applied in a thin layer to the surface of the fibre-reinforced synthetic resin body. Any methods which are suitable for this can be used. The application can be carried out for example by hand with a spatula, mechanically with a doctor blade, by a spraying operation or, according to an "inverse method". The "inverse method" involves inflating a body, especiaIly a cylinder or a tube, against a correspondingly shaped mould, the inner wall of which has been provided with a synthetic resin and particle 2 ~
layer, curing of the synthetic resin and subsequent removal from the mould. According to another variant of such an "inverse method", a synthetic resin is used which expands during tempera-ture treatment and/or during curing. The particles may possibly be contained in -the expandable synthetic resin or in a synthetic resin layer applied to the inner wall of the surrounding mould.
For coatings which do not need to satisfy any high demands, the particles can also be sprinkled on to a synthetic resin layer or sprayed on as powder and, if necessary, pressed in. After its production, the particle-containing layer is cured according to known methods.
When high demands are made of the dimensional accuracy of the finished coated body, it is advantageous to provide the fibre-reinforced base body with a surface which is machined to suitable tolerances. This can be carried out, according to use, by a grinding or machining operation. In order to obtain a smooth undeformed surface after the application of the particle-containing synthetic resin layer and the curing of this layer, the body provided with the particle-containing synthetic resin layer may be coated with a covering foil which is removed after curing. For this purpose, a cylindrical body may be wound with a covering band in a manner known in the art. The thickness of the layer located on the fibre-containing base body and containing particles acting as agent for the bonding of the thermally sprayed-on layer is not particularly critical and is generally from 50 ~m to 4,000 ~m. The layer thinner than 50 ~m is unlikely to permit sufficient thermal compensation during thermal spraying 2 0 ~ 9 and tends to result in a break bonding. On the other hand, the layer thicker than 4,000 ~m may not be very favourable because of increased consumption oE material, increased weight of the whole body and because of difficulty of applying the coating in a dimensionally accurate manner. The particles which act as a bonding agent may be introduced into the synthetic resin in granular or powder form. The amount of the particles may vary in a wide range according to requirements in each case, is preferably between 5 and 60 percent by volume, relative to the mixture of the synthetic resin and the particles. The shape of the particles can vary in each case according to the origin of the material and the method of its production. The most frequently used forms are essentially isometric, platelet or rod shape while those having angular, rough or serrated particle surfaces tend to form firm anchoring and thus are preferred.
The particle size is not particularly critical and is generally from 10 ~m to 1,000 ~m.
The particles introduced into the body to be coated correspond to the materials of which the thermally sprayed-on layers are formed. These can be metals such as nickel, chromium, vanadium, manganese, iron, cobalt, titanium, silicon, alloys of these metals or aluminium or alloys thereof or copper and alloys thereof or non-metallic substances such as silicon dioxide, glass, aluminium oxide, titanium dioxide, zirconium dioxide or Si-SiC. With the coating as a whole in mind, proceeding from the requirements for the thermally sprayed-on layer, a material is chosen which results in good bonding to the material of the thermally sprayed-on layer and which can be firmly anchored in 2 ~ 9 particle form in the resin matrix. At the same time, it is not necessary that the particles anchored in the synthetic resin consist of the same material as the thermally sprayed-on layer.
After curiny the layer containing the particles, the synthetic resin skin initially covering the particles is removed.
This is absolutely necessary for the further success of the method according to the invention for good chemical bonding to be achieved between the thermally sprayed-on layer and the particles acting as agent for the bonding of this layer to the fibre-reinforced body. The removal may be accomplished, for example, by a mechanical removal, by a chemical dissolution or an etching process. Particularly advantageous as the mechanical removal are machine grinding and sand or powder blasting. The relatively smooth particle surfaces obtained in this way can subsequently be roughened, for example by a chemical etching with an acid or an alkali, without damaging the smooth synthetic resin surface of the body. The term "chemical bonding" in the present invention includes any types of chemical bonding such as ionogenic, covalent, metallic and dative bonding.
When dimensionally accurate coated parts such as rollers for the printing industry are to be manufactured, it is advantageous to grind to size the surface of the cylinder blank after application of the particle-containing layer but before the thermal coating, to form a smooth surface. The layers which are subse~uently sprayed on thermally and possibly layers which are applied additionally then have a more uniform layer structure and a more uniform layer thickness and can be brought to the 2 ~
required size and required surface quality at a lower cost.
At least one layer is sprayed on to the fibre-reinforced synthetic resin body premachined as described above, which body has a particle-containing zone on the outside, by means of a known thermal spraying method. Flame spraying and plasma spraying, in par~icular, including variants oE vacuum plasma spraying, are possible as the method of application. The resistant coating layer is typically formed of a resistant metal such as nickPl or an alloy mainly composed of nickel. The resistant coating layer may also be formed of a ceramic material such as aluminium oxide.
Any of the substances listed above as dispersion material in particle form for the synthetic resin intermediate layer can be used as spraying material. The selection of the substance used in each case depends on the specific application.
The application also determines the structure of the surface of the body. The coated body can frequently be used without further surface treatment for uses in the building industry or in abrasion protection. Uses in mechanical engineering such as, for example, printing, inking, idle or feed rollers in paper or foil production or processing require subsequent processing by metal removal machining operations, by grinding, polishing or lapping, in order to achieve the necessary degree of precision and surface roughness.
Many uses require the production of bodies with a multi-layer coating on the base body containing synthetic resin. This can be the case, for example, when, on the outside, a ductile surface is required which is supported on a hard tough subs~rate ~06~1~9 or, in general terms, when the application of a primary layer alone is not sufficient for the intended use, and the required properties of the coating with regard to hardness, roughness, adhesion, porosity, electrical conductivity, surface structure etc., can only be achieved by applying further layers. In these cases it is possible to apply further layers to the first thermally sprayed-on layer, according to methods known per se and tested in practice. This can be carried out by continuing the application with thermal spraying methods or, if the primary layer is electrically conductive, even electrolytically. In this way, several layers can be applied one on top of another.
The application method used may vary from layer to layer. The materials which are applied in Iayers one on top of another are usually formed from different substances. However, they can also be of identical material.
As can be seen, the method according to the invention can be varied a great deal and permits, in a simple way, adaptation to a large number of approaches to technical problems.
In detail, the following advantages result. It is now possible to produce, in a simple way, on fibre-reinforced synthetic resin bodies, by means of a thermal spraying method, surface coatings with considerably improved ad~esion and mechanical stability in comparison to the prior art. The earlier problems of bonding existing between the thermally sprayed-on layer and the fibre-reinforced synthetic resin body, which were caused by:
1) the effect of great differences in thermal expansion coefficients between the fibre-reinforced synthetic resin body 2 ~
and the thermally sprayed-on coating material and 2) the formation of decomposition products of the synthetic resin during the thermal spraying and 3) the production of such decomposition products during thermal spraying and/or the presence of a synthetic resin inter-mediate layer between layers applied additionally to the fibre-reinforced synthetic resin body in order to produce better bonding of the sprayed-on layers, and the thermally sprayed-on layer, have become practically insignificant for the thermal spraying-on of the layers and for the stressing of these layers in the course of operation. The lack of sensitivity and the good adhesion of the coating can be seen in the fact that bodies coated using the method according to the invention can be cut with mechanical cutting tools without parts of the layer being chipped off, and that the coating stands up to impact stresses during handling and in operation, without damage. The application and preparation on the fibre-reinforced base body, of the layer required by the procedure and determining the improved adhesion, can take place according to methods which are simple and can also be carried out mechanically, and thus efficiently. Damage to outer reinforcing fibres by the impact of particles during thermal spraying can be excluded. The user of the method is free, within wide limits, in his choice of resin matrices for the reinforcing fibres and the materials for the layers to be applied.
The invention is explained by the following exemplifying embodiments. However, it is not limited to the embodiments in the examples.
2 ~
Example 1 A 2,000 mm long hollow cylinder having an internal diameter of 90 mm and made of phenol formaldehyde resin reinforced with carbon filaments was used as a starting material. The cylinder was produced by winding a carbon fibre saturated with phenol formaldehyde resin on to a cylindrical mandrel in a large number of layers, curing the resin, and removed from the mandrel.
The cylinder was ground to size on a turning lathe so that it had an outside diameter of 100 mm. For coating with a synthetic resin layer filled with a metal powder, the cylinder prepared in this way was clamped on to a digitally controlled winding machine and its outer surface was degreased with acetone. The composition for the coating consist~d of a mixture of phenol formaldehyde resin (Bakelite* DW 247), with a viscosity of 500 to 1,000 mPa-s and water-atomized steel powder (type 316 L) which is rust-free and has a granular size < 75 ~m in the volume ratio 45% steel powder to 55% phenol formaldehyde resin. For the coating, the cylinder was rotated at a speed of 30 m/min and the coating mixture was applied with a flexible spatula to a thickness of approximately 1 mm. Subsequently, the coated body was wrapped around with a tear-off fabric and cured in a circulating air drying cabinet with the following hardening cycle:
Heating to 90C, 1 hour, Holding time at 90C, 24 hours, Heating from 90C to 130C, l hour, Holding time at 130C, 2 hours~
Trade-mark 2 ~ 9 25861~18 Cooling to room temperature without active cooling.
The cylinder having the cured surface layer was ground to size to a diameter of 100.8 mm and a surface roughness of lO
to 15 ~m, on a grinding machine with a diamond wheel and its outer surface was dusted off by blowing with oil mist-free compressed air. A layer made of a nickel/chromium alloy (80% by weight nickel, 20~ by weight chromium) was applied to the lateral surface of the cylinder prepared in this way by plasma spraying and applying the conventional conditions for this technical field. After the spray treatment, the peaks and edges of the applied coating were removed by brushing with a wire brush and a smooth surface was obtained.
Example 2 A large carbon fibre cable made up of 40,0Q0 filaments which had been led through a bath of an epoxy resin (Bakelite*
L 20) with viscosity 800 to l,000 mPa s, was wound on a winding machine, on to a mandrel 90 mm in diameter to a layer thickness of approximately 9.5 mm. The wound body had a length of 1,500 mm.
For introducing the metal-containing laver of bonding agent into the outer layers of the wound body, work was continued with a carbon fibre cable made up of 12,000 filaments. This cable was led through a bath which consisted of a suspension made of the same epoxy resin as above (Bakelite* L 20) with a content of 50~
by weight (= 15% by volume) of an alloy powder having a granular size 60% < 70 ~m and a composition of 89% by weight nickel, 5 by weight molybdenum and 6~ by weight aluminium, and, after passing through the bath until a wall thickness of approximately lO.l mm had been achieved, the cable was wound on to the cylinder.
~ 17 - 2 ~ ~2~6~918 Because of the fibre tension during winding, a considerable part of the mixture of epoxy resin and alloy powder was pressed out of the wound layers applied in this way, into the outer surface layer, so that a thin, fibre-free layer of synthetic resin and alloy powder was formed there. The surface of the wound body was wrapped around with a separating foil and cured in a circulating air drying cabinet with the following hardening cycle:
Heating to 90C, 1 hour, Holding time at 90C, 10 hours, Heating from 90C to 130C, 1 hour, Holding time at 130C, 2 hours.
The cylinder obtained in this way was then yround on a turning lathe with a diamond grinding wheel to a final size of 10.0 mm. For coating the cylinder after the flame spraying operation, the cylinder was clamped after grinding, into a motor-dri.ven turning device which enabled rotation of the cylinder around the longitudinal axis. Before the start of the spraying operation, the surface of the cylinder was cleansed of particles of dust adhering to it by means of oil mist-free compressed air. Subsequently, the lateral surface of the cylinder was coated with a 100 ~m thick layer made of an alloy composed of 78~ by weight nickel, 15% by weight chromium, 7~ by weight iron by the flame spraying procedure under conventional conditions for this branch of technology. After coating, the surface of the cylinder was smoothed by removing the peaks by means of a steel brush.
- 1~ 20~6~
Example 3 A mixture of phenol formaldehyde resin (Bakelite* DW
247, viscosity 500 to l,OOC mPa-s) with an alloy powder Igrain sizes 100 to 200 ~m, composition: nickel 80% by weight, chromium 20% by weight) in the volume ratio 55% alloy powder, 45% phenol formaldehyde resin was applied with a spatula, to a plate (width 30 cm, length 50 cm, thickness 0.2 cm) reinforced with glass fibres (average length 20 mm) and made of phenol formaldehyde resin, the surface of which had been freed of dust with oil mist-free compressed air, to a layer thickness of 1 mm.
For hardening the layer applied, the plate was placed in a circulating air drying cabinet and cured according to the harden-ing cycle described in Example 1. After curing, the surface of the plate was treated with a sand blaster until approximately 0.1 mm of the cured resin layer applied to the surface of the plate and containing alloy powder had been removed and sufficient surface portions of the grains of alloy powder dispersed in the resin layer had been blasted free of resin. After blowing free of dust with oil mist-free compressed air/ the blasted surface was provided with an aluminium oxide layer (layer thickness 500 ~m) in a plasma spraying installation having a two~coordinate traversing device (horizontal, vertical). The coating thus obtained can be used without further machining for the purpose of abrasion protection.
The thermally sprayed-on layers produced in with the coatings according to Examples 1, 2 and 3 were compared with layers of identical composition which had been manufactured 2~661~9 without the use of an intermediate layer enabling bonding, using coating methods according to the prior art~ The test methods and types of stress applied, and the test results obtained and observations made, can be seen from the tabulated summary.
2 ~ 9 _, _ _ . _ D 3 o ~ C~, ~ ~
c c a~ .
a ~ a~ '~ ~ ,C
' ~> c~
. .
~ ~ C
~ ~ F~ ~e~ o~ c a ~ ~ a. ~ ~ ~.
_ I
~ C~ n ~Ccn ~ C
,G ,~ ~ C
C ~ C O ~ J C ~ ~
.~ ~ D " a~ æ ~ ", C O ~ -~ O ~
~,:~> 'V~ ~ ~ '~0 ~ ~ ~o ,~, aO~ ~0 _ _ _ I
~; El O ~0 <~
C-~ _C ~ O ` ~ ~ O
~ ~ ~ a~ ~ a~ a a -"
E~ C7 a~ ~ ~ ", . ~; El _~ ,~ ~ ," C C '~
~3 4-0~ )- ~ ~ ~ ~ O L~ ~
I_ cn C ~0 ~ ~ O ~ _C ~ tcn ~ ,~ c~ rn æ -~, - c a ~ r~ _ ~) C ~ D ~ O q) C~ r J ra ~ =~ _ _C O >~ ~ C~
rV ~
_~ O ~ ~ :S -~ G
._ ~ ~ ~ 53 ~>
E_ ~ ~ ~a~ C
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_C C ~ r~ ~
__ -_ rV ~ I_ ~ ~ ~ ~: O
rA
r~ ~C V ~ ~
r~ C ,t~ r~
~ r J ~ ~ ~ r J
- 21 - 2~
2sa6l-ls To these observatlons and results it must be added that coating operatlons such as those carried out in Examples 1, 2 and 3, but without first freeing and cleansing from synthetic resin the bonding surfaces of S the particles incorporated in the synthetic resin lntermedlate layer, only achieve adhesion of the quality ln the comparison example to Example 1.
The results described show clearly the technical progress brought about by the invention.
The base body made of fibre-reinforced plastics may have any shape suitable for the use of a thermal spraying method.
20~6~9 A group of preferred bodies are flat or curved areal moulded bodies such as plates, bowls, containers or pipelines or segments thereof. Another group of preferable bodies have at least partially closed surfaces such as pipes, rollers, cylinders, cones or truncated cones.
Any synthetic resins from which bodies of the shape described above can be manufactured with sufficient stability of shape and temperature can be used as the base material and matrix material for the reinforcing fibres. In particular, preferred are thermosetting resins such as phenol formaldehyde, epoxy or polyester resins. However, thermoplastic resins such as, for example, polypropylene, polyamide or polycarbonate are also suitable. Carbon fibres (with graphite ibres being included in this term), glass fibres and arylamide fibres are particularly preferred as the reinforcing fibres. Where useful, other fibres, for example mineral fibres such as basalt fibres or rock wool, metal fibres and carbide fibres such as SiC whiskers, can also be used. The fibres can be incorporated into the synthetic resin body as short-chopped fibres or staple fibres, in the form of woven cloth, nets, knitted fabrics or other textile formations of two-dimensional or three-dimensional kind, or as continuous filaments.
Serving to provide bonding for the layer to be sprayed on thermally are particles which are incorporated either:
1) directly into a layer adjacent to the outer surface of the fibre-reinforced base body or 2) in a layer applied to the outer surface of the fibre-reinforced base body and firmly bonded to this surface.
2~6~9 In the first case, the particles are worked in directly during the formation of the outermost layers. The particles in the dry state can be processed. The particles may also be provided with a bonding agent or suspended in a resin or in a resin solution. This can take place, for example, by the simultaneous spraying-on of the particles and a short-fibre-reinforced synthetic resin material, using separate spraying devices operating in coordinated manner, or by the spraying-on of the synthetic resin containing the particles in a suitable manner, or by sprinkling the dry particles during the formation of a body reinforced with filaments, for example during the winding process.
In the second case, there is produced in an advantageous manner a mixture made of a synthetic resin which can bond well to the base body made of fibre-reinforced synthetic resin, and the particles. The synthetic resin selected for this purpose may be the same as that of the base body or it may be another which is capable of bonding well to the base body, of retaining well the particles and of being well machined after curing. This mixture of the synthetic resin and the particles is applied in a thin layer to the surface of the fibre-reinforced synthetic resin body. Any methods which are suitable for this can be used. The application can be carried out for example by hand with a spatula, mechanically with a doctor blade, by a spraying operation or, according to an "inverse method". The "inverse method" involves inflating a body, especiaIly a cylinder or a tube, against a correspondingly shaped mould, the inner wall of which has been provided with a synthetic resin and particle 2 ~
layer, curing of the synthetic resin and subsequent removal from the mould. According to another variant of such an "inverse method", a synthetic resin is used which expands during tempera-ture treatment and/or during curing. The particles may possibly be contained in -the expandable synthetic resin or in a synthetic resin layer applied to the inner wall of the surrounding mould.
For coatings which do not need to satisfy any high demands, the particles can also be sprinkled on to a synthetic resin layer or sprayed on as powder and, if necessary, pressed in. After its production, the particle-containing layer is cured according to known methods.
When high demands are made of the dimensional accuracy of the finished coated body, it is advantageous to provide the fibre-reinforced base body with a surface which is machined to suitable tolerances. This can be carried out, according to use, by a grinding or machining operation. In order to obtain a smooth undeformed surface after the application of the particle-containing synthetic resin layer and the curing of this layer, the body provided with the particle-containing synthetic resin layer may be coated with a covering foil which is removed after curing. For this purpose, a cylindrical body may be wound with a covering band in a manner known in the art. The thickness of the layer located on the fibre-containing base body and containing particles acting as agent for the bonding of the thermally sprayed-on layer is not particularly critical and is generally from 50 ~m to 4,000 ~m. The layer thinner than 50 ~m is unlikely to permit sufficient thermal compensation during thermal spraying 2 0 ~ 9 and tends to result in a break bonding. On the other hand, the layer thicker than 4,000 ~m may not be very favourable because of increased consumption oE material, increased weight of the whole body and because of difficulty of applying the coating in a dimensionally accurate manner. The particles which act as a bonding agent may be introduced into the synthetic resin in granular or powder form. The amount of the particles may vary in a wide range according to requirements in each case, is preferably between 5 and 60 percent by volume, relative to the mixture of the synthetic resin and the particles. The shape of the particles can vary in each case according to the origin of the material and the method of its production. The most frequently used forms are essentially isometric, platelet or rod shape while those having angular, rough or serrated particle surfaces tend to form firm anchoring and thus are preferred.
The particle size is not particularly critical and is generally from 10 ~m to 1,000 ~m.
The particles introduced into the body to be coated correspond to the materials of which the thermally sprayed-on layers are formed. These can be metals such as nickel, chromium, vanadium, manganese, iron, cobalt, titanium, silicon, alloys of these metals or aluminium or alloys thereof or copper and alloys thereof or non-metallic substances such as silicon dioxide, glass, aluminium oxide, titanium dioxide, zirconium dioxide or Si-SiC. With the coating as a whole in mind, proceeding from the requirements for the thermally sprayed-on layer, a material is chosen which results in good bonding to the material of the thermally sprayed-on layer and which can be firmly anchored in 2 ~ 9 particle form in the resin matrix. At the same time, it is not necessary that the particles anchored in the synthetic resin consist of the same material as the thermally sprayed-on layer.
After curiny the layer containing the particles, the synthetic resin skin initially covering the particles is removed.
This is absolutely necessary for the further success of the method according to the invention for good chemical bonding to be achieved between the thermally sprayed-on layer and the particles acting as agent for the bonding of this layer to the fibre-reinforced body. The removal may be accomplished, for example, by a mechanical removal, by a chemical dissolution or an etching process. Particularly advantageous as the mechanical removal are machine grinding and sand or powder blasting. The relatively smooth particle surfaces obtained in this way can subsequently be roughened, for example by a chemical etching with an acid or an alkali, without damaging the smooth synthetic resin surface of the body. The term "chemical bonding" in the present invention includes any types of chemical bonding such as ionogenic, covalent, metallic and dative bonding.
When dimensionally accurate coated parts such as rollers for the printing industry are to be manufactured, it is advantageous to grind to size the surface of the cylinder blank after application of the particle-containing layer but before the thermal coating, to form a smooth surface. The layers which are subse~uently sprayed on thermally and possibly layers which are applied additionally then have a more uniform layer structure and a more uniform layer thickness and can be brought to the 2 ~
required size and required surface quality at a lower cost.
At least one layer is sprayed on to the fibre-reinforced synthetic resin body premachined as described above, which body has a particle-containing zone on the outside, by means of a known thermal spraying method. Flame spraying and plasma spraying, in par~icular, including variants oE vacuum plasma spraying, are possible as the method of application. The resistant coating layer is typically formed of a resistant metal such as nickPl or an alloy mainly composed of nickel. The resistant coating layer may also be formed of a ceramic material such as aluminium oxide.
Any of the substances listed above as dispersion material in particle form for the synthetic resin intermediate layer can be used as spraying material. The selection of the substance used in each case depends on the specific application.
The application also determines the structure of the surface of the body. The coated body can frequently be used without further surface treatment for uses in the building industry or in abrasion protection. Uses in mechanical engineering such as, for example, printing, inking, idle or feed rollers in paper or foil production or processing require subsequent processing by metal removal machining operations, by grinding, polishing or lapping, in order to achieve the necessary degree of precision and surface roughness.
Many uses require the production of bodies with a multi-layer coating on the base body containing synthetic resin. This can be the case, for example, when, on the outside, a ductile surface is required which is supported on a hard tough subs~rate ~06~1~9 or, in general terms, when the application of a primary layer alone is not sufficient for the intended use, and the required properties of the coating with regard to hardness, roughness, adhesion, porosity, electrical conductivity, surface structure etc., can only be achieved by applying further layers. In these cases it is possible to apply further layers to the first thermally sprayed-on layer, according to methods known per se and tested in practice. This can be carried out by continuing the application with thermal spraying methods or, if the primary layer is electrically conductive, even electrolytically. In this way, several layers can be applied one on top of another.
The application method used may vary from layer to layer. The materials which are applied in Iayers one on top of another are usually formed from different substances. However, they can also be of identical material.
As can be seen, the method according to the invention can be varied a great deal and permits, in a simple way, adaptation to a large number of approaches to technical problems.
In detail, the following advantages result. It is now possible to produce, in a simple way, on fibre-reinforced synthetic resin bodies, by means of a thermal spraying method, surface coatings with considerably improved ad~esion and mechanical stability in comparison to the prior art. The earlier problems of bonding existing between the thermally sprayed-on layer and the fibre-reinforced synthetic resin body, which were caused by:
1) the effect of great differences in thermal expansion coefficients between the fibre-reinforced synthetic resin body 2 ~
and the thermally sprayed-on coating material and 2) the formation of decomposition products of the synthetic resin during the thermal spraying and 3) the production of such decomposition products during thermal spraying and/or the presence of a synthetic resin inter-mediate layer between layers applied additionally to the fibre-reinforced synthetic resin body in order to produce better bonding of the sprayed-on layers, and the thermally sprayed-on layer, have become practically insignificant for the thermal spraying-on of the layers and for the stressing of these layers in the course of operation. The lack of sensitivity and the good adhesion of the coating can be seen in the fact that bodies coated using the method according to the invention can be cut with mechanical cutting tools without parts of the layer being chipped off, and that the coating stands up to impact stresses during handling and in operation, without damage. The application and preparation on the fibre-reinforced base body, of the layer required by the procedure and determining the improved adhesion, can take place according to methods which are simple and can also be carried out mechanically, and thus efficiently. Damage to outer reinforcing fibres by the impact of particles during thermal spraying can be excluded. The user of the method is free, within wide limits, in his choice of resin matrices for the reinforcing fibres and the materials for the layers to be applied.
The invention is explained by the following exemplifying embodiments. However, it is not limited to the embodiments in the examples.
2 ~
Example 1 A 2,000 mm long hollow cylinder having an internal diameter of 90 mm and made of phenol formaldehyde resin reinforced with carbon filaments was used as a starting material. The cylinder was produced by winding a carbon fibre saturated with phenol formaldehyde resin on to a cylindrical mandrel in a large number of layers, curing the resin, and removed from the mandrel.
The cylinder was ground to size on a turning lathe so that it had an outside diameter of 100 mm. For coating with a synthetic resin layer filled with a metal powder, the cylinder prepared in this way was clamped on to a digitally controlled winding machine and its outer surface was degreased with acetone. The composition for the coating consist~d of a mixture of phenol formaldehyde resin (Bakelite* DW 247), with a viscosity of 500 to 1,000 mPa-s and water-atomized steel powder (type 316 L) which is rust-free and has a granular size < 75 ~m in the volume ratio 45% steel powder to 55% phenol formaldehyde resin. For the coating, the cylinder was rotated at a speed of 30 m/min and the coating mixture was applied with a flexible spatula to a thickness of approximately 1 mm. Subsequently, the coated body was wrapped around with a tear-off fabric and cured in a circulating air drying cabinet with the following hardening cycle:
Heating to 90C, 1 hour, Holding time at 90C, 24 hours, Heating from 90C to 130C, l hour, Holding time at 130C, 2 hours~
Trade-mark 2 ~ 9 25861~18 Cooling to room temperature without active cooling.
The cylinder having the cured surface layer was ground to size to a diameter of 100.8 mm and a surface roughness of lO
to 15 ~m, on a grinding machine with a diamond wheel and its outer surface was dusted off by blowing with oil mist-free compressed air. A layer made of a nickel/chromium alloy (80% by weight nickel, 20~ by weight chromium) was applied to the lateral surface of the cylinder prepared in this way by plasma spraying and applying the conventional conditions for this technical field. After the spray treatment, the peaks and edges of the applied coating were removed by brushing with a wire brush and a smooth surface was obtained.
Example 2 A large carbon fibre cable made up of 40,0Q0 filaments which had been led through a bath of an epoxy resin (Bakelite*
L 20) with viscosity 800 to l,000 mPa s, was wound on a winding machine, on to a mandrel 90 mm in diameter to a layer thickness of approximately 9.5 mm. The wound body had a length of 1,500 mm.
For introducing the metal-containing laver of bonding agent into the outer layers of the wound body, work was continued with a carbon fibre cable made up of 12,000 filaments. This cable was led through a bath which consisted of a suspension made of the same epoxy resin as above (Bakelite* L 20) with a content of 50~
by weight (= 15% by volume) of an alloy powder having a granular size 60% < 70 ~m and a composition of 89% by weight nickel, 5 by weight molybdenum and 6~ by weight aluminium, and, after passing through the bath until a wall thickness of approximately lO.l mm had been achieved, the cable was wound on to the cylinder.
~ 17 - 2 ~ ~2~6~918 Because of the fibre tension during winding, a considerable part of the mixture of epoxy resin and alloy powder was pressed out of the wound layers applied in this way, into the outer surface layer, so that a thin, fibre-free layer of synthetic resin and alloy powder was formed there. The surface of the wound body was wrapped around with a separating foil and cured in a circulating air drying cabinet with the following hardening cycle:
Heating to 90C, 1 hour, Holding time at 90C, 10 hours, Heating from 90C to 130C, 1 hour, Holding time at 130C, 2 hours.
The cylinder obtained in this way was then yround on a turning lathe with a diamond grinding wheel to a final size of 10.0 mm. For coating the cylinder after the flame spraying operation, the cylinder was clamped after grinding, into a motor-dri.ven turning device which enabled rotation of the cylinder around the longitudinal axis. Before the start of the spraying operation, the surface of the cylinder was cleansed of particles of dust adhering to it by means of oil mist-free compressed air. Subsequently, the lateral surface of the cylinder was coated with a 100 ~m thick layer made of an alloy composed of 78~ by weight nickel, 15% by weight chromium, 7~ by weight iron by the flame spraying procedure under conventional conditions for this branch of technology. After coating, the surface of the cylinder was smoothed by removing the peaks by means of a steel brush.
- 1~ 20~6~
Example 3 A mixture of phenol formaldehyde resin (Bakelite* DW
247, viscosity 500 to l,OOC mPa-s) with an alloy powder Igrain sizes 100 to 200 ~m, composition: nickel 80% by weight, chromium 20% by weight) in the volume ratio 55% alloy powder, 45% phenol formaldehyde resin was applied with a spatula, to a plate (width 30 cm, length 50 cm, thickness 0.2 cm) reinforced with glass fibres (average length 20 mm) and made of phenol formaldehyde resin, the surface of which had been freed of dust with oil mist-free compressed air, to a layer thickness of 1 mm.
For hardening the layer applied, the plate was placed in a circulating air drying cabinet and cured according to the harden-ing cycle described in Example 1. After curing, the surface of the plate was treated with a sand blaster until approximately 0.1 mm of the cured resin layer applied to the surface of the plate and containing alloy powder had been removed and sufficient surface portions of the grains of alloy powder dispersed in the resin layer had been blasted free of resin. After blowing free of dust with oil mist-free compressed air/ the blasted surface was provided with an aluminium oxide layer (layer thickness 500 ~m) in a plasma spraying installation having a two~coordinate traversing device (horizontal, vertical). The coating thus obtained can be used without further machining for the purpose of abrasion protection.
The thermally sprayed-on layers produced in with the coatings according to Examples 1, 2 and 3 were compared with layers of identical composition which had been manufactured 2~661~9 without the use of an intermediate layer enabling bonding, using coating methods according to the prior art~ The test methods and types of stress applied, and the test results obtained and observations made, can be seen from the tabulated summary.
2 ~ 9 _, _ _ . _ D 3 o ~ C~, ~ ~
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I_ cn C ~0 ~ ~ O ~ _C ~ tcn ~ ,~ c~ rn æ -~, - c a ~ r~ _ ~) C ~ D ~ O q) C~ r J ra ~ =~ _ _C O >~ ~ C~
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- 21 - 2~
2sa6l-ls To these observatlons and results it must be added that coating operatlons such as those carried out in Examples 1, 2 and 3, but without first freeing and cleansing from synthetic resin the bonding surfaces of S the particles incorporated in the synthetic resin lntermedlate layer, only achieve adhesion of the quality ln the comparison example to Example 1.
The results described show clearly the technical progress brought about by the invention.
Claims (18)
1. A method for the application of a firmly adhering resistant coating layer to a body made of a composite material comprising reinforcing fibres and a plastic matrix, which process comprises:
(A) providing the body having an outer layer made of a synthetic resin containing particles of a material incorporated therein which corresponds to or is capable of chemically bonding with a material of the resistant coating layer;
(B) removing a surface of the outer layer to such an extent and in such a way that the particles have a clean exposed surface free from the synthetic resin and pointing in the direction of the later resistant coating; and (C) spraying the material of the resistant coating layer onto the surface by means of a thermal spraying process.
(A) providing the body having an outer layer made of a synthetic resin containing particles of a material incorporated therein which corresponds to or is capable of chemically bonding with a material of the resistant coating layer;
(B) removing a surface of the outer layer to such an extent and in such a way that the particles have a clean exposed surface free from the synthetic resin and pointing in the direction of the later resistant coating; and (C) spraying the material of the resistant coating layer onto the surface by means of a thermal spraying process.
2. The method according to claim 1, wherein the outer layer of the synthetic resin containing the particles has a thickness of from 50 µm to 4,000 µm, and the particles are incorporated in an amount of 5 to 60% by volume relative to the total amount of the particles and the synthetic resin.
3. The method according to claim 1, wherein the particles have a size of from 10 µm to 1,000 µm.
4. The method according to claim 1, 2 or 3, wherein the particles and the material used for the thermal spraying are each made of a metal selected from the group consisting of (a) nickel, chromium, vanadium, manganese, iron, cobalt, titanium, silicon, or alloys of these metals, (b) aluminium or aluminium alloys, and (c) copper or copper alloys.
5. The method according to claim 1, 2 or 3, wherein the particles and the material used for the thermal spraying are each made of a non-metallic substance selected from the group consisting of silicon dioxide, aluminium oxide, titanium oxide, zirconium oxide and silicon carbide/silicon.
6. The method according to claim 1, 2 or 3, wherein the composite material is reinforced with short fibres.
7. The method according to claim 1, 2 or 3, wherein the composite material is reinforced with filaments.
8. The method according to claim 1, 2 or 3, wherein the composite material is reinforced with textile structures obtained by textile linkage of fibres.
9. The method according to claim 1, 2 or 3, wherein the outer firmly adhering, resistant layer is applied by flame spraying.
10. The method according to claim l, 2 or 3, wherein the outer firmly adhering, resistant adhesive layer is applied by plasma spraying.
11. The method according to claim 1, 2 or 3, which further comprises thermally spraying at least one further layer onto the thermally sprayed-on layer.
12. The method according to claim 1, 2 or 3, which further comprises electrolytically depositing at least one layer on the thermally sprayed-on layer.
13. The method according to claim 1, 2 or 3, wherein the body to be coated is a cylinder or roller made of carbon fibre-reinforced synthetic resin.
14. A method for the application of a firmly adhering abrasion-resistant coating layer of a metal or ceramic material to a body made of a composite material comprising reinforcing fibres and a plastic matrix, which process comprises:
[A] on a surface of the body, forming an outer layer which is firmly bonded to the body, has a thickness of 50 µm to 4,000 µm and is made of a cured synthetic resin containing particles of a material incorporated therein, the said material of the particles being a metal or ceramic and being capable of chemically bonding to the material of the abrasion-resistant coating layer, wherein the outer layer is formed as an outermost part of the body during the production of the body or is formed as an additional layer after the production of the body;
[B] removing a surface of the outer layer to such an extent and in such a way that the particles have a clean exposed surface free from the synthetic resin and pointing in the direction of the later abrasion-resistant coating and are firmly anchored to the cured synthetic resin of the outer layer; and [C] spraying the material of the abrasion-resistant coating onto the thus-treated surface by means of a thermal spray process, thereby anchoring particles sprayed on the surface to the particles by a chemical bond.
[A] on a surface of the body, forming an outer layer which is firmly bonded to the body, has a thickness of 50 µm to 4,000 µm and is made of a cured synthetic resin containing particles of a material incorporated therein, the said material of the particles being a metal or ceramic and being capable of chemically bonding to the material of the abrasion-resistant coating layer, wherein the outer layer is formed as an outermost part of the body during the production of the body or is formed as an additional layer after the production of the body;
[B] removing a surface of the outer layer to such an extent and in such a way that the particles have a clean exposed surface free from the synthetic resin and pointing in the direction of the later abrasion-resistant coating and are firmly anchored to the cured synthetic resin of the outer layer; and [C] spraying the material of the abrasion-resistant coating onto the thus-treated surface by means of a thermal spray process, thereby anchoring particles sprayed on the surface to the particles by a chemical bond.
15. The method according to claim 14, wherein the particles have a size of from 10 µm to 1,000 µm and are incorporated in the outer layer in step [A] in an amount of 5 to 60% by volume relative to the total amount of the particles and the synthetic resin.
16. The method according to claim 15, wherein the particles and the abrasion-resistant coating layer are each made of a member selected from the group consisting of (a) nickel, chromium, vanadium, manganese, iron, cobalt, titanium, silicon or an alloy of one of these metals, (b) aluminium or an alloy thereof, (c) copper or an alloy thereof, (d) silicon dioxide, (e) aluminium dioxide, (f) titanium dioxide, (g) zirconium oxide and (h) silicon carbide/silicon.
17. The method according to claim 14, 15 or 16, wherein the plastic matrix of the body and the synthetic resin of the outer layer are of the same resin.
18. The method according to claim 17, wherein the resin is phenol formaldehyde resin.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4116641A DE4116641A1 (en) | 1991-05-22 | 1991-05-22 | METHOD FOR COATING A FIBER REINFORCED PLASTIC BODY |
| DEP4116641.8 | 1991-05-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2066149A1 true CA2066149A1 (en) | 1992-11-23 |
Family
ID=6432141
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002066149A Abandoned CA2066149A1 (en) | 1991-05-22 | 1992-04-15 | Method for coating a fibre-reinforced plastics body |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP0514640B1 (en) |
| JP (1) | JP2954423B2 (en) |
| KR (1) | KR920021629A (en) |
| AT (1) | ATE113633T1 (en) |
| CA (1) | CA2066149A1 (en) |
| DE (2) | DE4116641A1 (en) |
| FI (1) | FI99028C (en) |
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| DE102019213905A1 (en) * | 2019-09-12 | 2021-03-18 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Method for producing a composite component which is formed with a fiber-reinforced plastic component on which at least one surface is formed with a coating |
| KR102265884B1 (en) * | 2020-09-22 | 2021-06-16 | 한국건설기술연구원 | Concrete structure for repairing and strengthening using textile grid reinforcement and highly durable inorganic binder, and repair and strengthening method for the same |
| CN115254555A (en) * | 2022-07-12 | 2022-11-01 | 上海喆航航空科技有限公司 | Paint spraying and polishing method for surface of helicopter composite material part |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU456855A1 (en) * | 1972-08-15 | 1975-01-15 | Method of plating the surface of plastic products | |
| AT358289B (en) * | 1974-01-22 | 1980-08-25 | Paturle Sa Ets | METHOD FOR TREATING THE SURFACE OF PARTS MADE FROM A MIXTURE |
| DE3136283C1 (en) * | 1981-09-12 | 1983-02-03 | Nukem Gmbh, 6450 Hanau | Process for metallizing carbon fiber reinforced plastic parts |
| GB8429772D0 (en) * | 1984-11-26 | 1985-01-03 | Ici Plc | Polymeric films |
| US4761217A (en) * | 1986-02-13 | 1988-08-02 | Dorsett Terry E | Electroplate to moving metal |
| DE3613060A1 (en) * | 1986-04-18 | 1987-10-22 | Herberts Gmbh | COATING AGENTS WITH HIGH ELECTRICAL CONDUCTIVITY AND THE USE THEREOF FOR THE PRODUCTION OF COATING |
| DE3644116A1 (en) * | 1986-12-23 | 1988-07-07 | Mtu Muenchen Gmbh | EROSION-RESISTANT COATING |
| JP2718957B2 (en) * | 1988-10-05 | 1998-02-25 | ポリプラスチックス株式会社 | Electrostatic coating method of crystalline thermoplastic resin molded product and painted plastics molded product |
| DE3844290C1 (en) * | 1988-12-30 | 1989-12-21 | Uranit Gmbh, 5170 Juelich, De | |
| US4997704A (en) * | 1989-06-02 | 1991-03-05 | Technetics Corporation | Plasma-arc ceramic coating of non-conductive surfaces |
| DE4014623A1 (en) * | 1990-05-08 | 1991-11-14 | Erbsloeh Julius & August | Coating non-metallic workpieces with functional layer - by dispersing particulate material in surface and partially by grinding etc. to provide intermediate layer which is easily coated |
-
1991
- 1991-05-22 DE DE4116641A patent/DE4116641A1/en not_active Withdrawn
-
1992
- 1992-03-14 KR KR1019920004207A patent/KR920021629A/en not_active Withdrawn
- 1992-03-16 AT AT92104515T patent/ATE113633T1/en not_active IP Right Cessation
- 1992-03-16 DE DE59200715T patent/DE59200715D1/en not_active Expired - Fee Related
- 1992-03-16 EP EP92104515A patent/EP0514640B1/en not_active Expired - Lifetime
- 1992-04-08 FI FI921549A patent/FI99028C/en active
- 1992-04-15 CA CA002066149A patent/CA2066149A1/en not_active Abandoned
- 1992-04-30 JP JP4137863A patent/JP2954423B2/en not_active Expired - Lifetime
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6982116B1 (en) | 2000-02-18 | 2006-01-03 | Praxair S.T. Technology, Inc. | Coatings on fiber reinforced composites |
| US6797331B2 (en) * | 2001-06-08 | 2004-09-28 | Man Roland Druckmaschinen Ag | Process for producing a chemical-resistant protective layer for a rotary body having a base body made from fiber-reinforced plastic |
| US7419704B2 (en) | 2005-08-18 | 2008-09-02 | Praxair S. T. Technology, Inc. | Coatings on fiber reinforced composites |
| GB2519444A (en) * | 2013-10-21 | 2015-04-22 | Boeing Co | Method of coating a composite material and a coated edge of a composite structure |
| GB2519444B (en) * | 2013-10-21 | 2016-08-17 | Boeing Co | Coating composite materials |
| EP3059333A1 (en) * | 2015-02-17 | 2016-08-24 | United Technologies Corporation | Toughened bond layer and method of production |
Also Published As
| Publication number | Publication date |
|---|---|
| DE4116641A1 (en) | 1992-11-26 |
| FI99028C (en) | 1997-09-25 |
| KR920021629A (en) | 1992-12-18 |
| JPH05202461A (en) | 1993-08-10 |
| EP0514640B1 (en) | 1994-11-02 |
| ATE113633T1 (en) | 1994-11-15 |
| DE59200715D1 (en) | 1994-12-08 |
| FI921549A0 (en) | 1992-04-08 |
| FI99028B (en) | 1997-06-13 |
| EP0514640A1 (en) | 1992-11-25 |
| JP2954423B2 (en) | 1999-09-27 |
| FI921549L (en) | 1992-11-23 |
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Legal Events
| Date | Code | Title | Description |
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| FZDE | Discontinued |