KR101771660B1 - sliding member sliding damper coating method using the coating composition and this - Google Patents
sliding member sliding damper coating method using the coating composition and this Download PDFInfo
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- KR101771660B1 KR101771660B1 KR1020150106718A KR20150106718A KR101771660B1 KR 101771660 B1 KR101771660 B1 KR 101771660B1 KR 1020150106718 A KR1020150106718 A KR 1020150106718A KR 20150106718 A KR20150106718 A KR 20150106718A KR 101771660 B1 KR101771660 B1 KR 101771660B1
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- 238000000576 coating method Methods 0.000 title claims abstract description 32
- 239000008199 coating composition Substances 0.000 title abstract description 10
- 239000000314 lubricant Substances 0.000 claims abstract description 35
- 239000000203 mixture Substances 0.000 claims abstract description 35
- 239000006255 coating slurry Substances 0.000 claims abstract description 34
- 239000011248 coating agent Substances 0.000 claims abstract description 23
- 239000003960 organic solvent Substances 0.000 claims abstract description 18
- 229920002312 polyamide-imide Polymers 0.000 claims abstract description 18
- 239000004810 polytetrafluoroethylene Substances 0.000 claims abstract description 18
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims abstract description 18
- 239000000843 powder Substances 0.000 claims abstract description 17
- 239000000758 substrate Substances 0.000 claims abstract description 17
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000004962 Polyamide-imide Substances 0.000 claims abstract description 15
- 229910021389 graphene Inorganic materials 0.000 claims abstract description 14
- 238000000034 method Methods 0.000 claims abstract description 13
- 239000011787 zinc oxide Substances 0.000 claims abstract description 13
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 12
- 239000004917 carbon fiber Substances 0.000 claims abstract description 12
- 229920000049 Carbon (fiber) Polymers 0.000 claims abstract description 11
- 241001455273 Tetrapoda Species 0.000 claims abstract description 11
- 239000002518 antifoaming agent Substances 0.000 claims abstract description 11
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims abstract description 11
- 230000001050 lubricating effect Effects 0.000 claims abstract description 8
- 239000002270 dispersing agent Substances 0.000 claims abstract description 6
- 238000001035 drying Methods 0.000 claims abstract description 6
- 230000001680 brushing effect Effects 0.000 claims abstract description 4
- 239000000919 ceramic Substances 0.000 claims abstract description 4
- 238000007645 offset printing Methods 0.000 claims abstract description 4
- 229920003023 plastic Polymers 0.000 claims abstract description 4
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- 238000005096 rolling process Methods 0.000 claims abstract description 4
- 238000007650 screen-printing Methods 0.000 claims abstract description 4
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- 230000003746 surface roughness Effects 0.000 claims abstract description 4
- 238000005238 degreasing Methods 0.000 claims abstract description 3
- 238000005406 washing Methods 0.000 claims abstract description 3
- 238000001354 calcination Methods 0.000 claims abstract 2
- 229920005989 resin Polymers 0.000 claims description 25
- 239000011347 resin Substances 0.000 claims description 25
- 239000007787 solid Substances 0.000 claims description 25
- 239000011230 binding agent Substances 0.000 claims description 17
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 14
- 239000008096 xylene Substances 0.000 claims description 14
- 239000013538 functional additive Substances 0.000 claims description 10
- 239000002055 nanoplate Substances 0.000 claims description 7
- 229920001187 thermosetting polymer Polymers 0.000 claims description 5
- 239000002245 particle Substances 0.000 claims description 3
- 238000001816 cooling Methods 0.000 claims description 2
- 238000003801 milling Methods 0.000 claims description 2
- MHABMANUFPZXEB-UHFFFAOYSA-N O-demethyl-aloesaponarin I Natural products O=C1C2=CC=CC(O)=C2C(=O)C2=C1C=C(O)C(C(O)=O)=C2C MHABMANUFPZXEB-UHFFFAOYSA-N 0.000 claims 2
- 239000012530 fluid Substances 0.000 claims 1
- 239000002002 slurry Substances 0.000 abstract description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N zinc oxide Inorganic materials [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 20
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 13
- 239000000463 material Substances 0.000 description 11
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 10
- 238000005299 abrasion Methods 0.000 description 10
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 9
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 8
- 229910052782 aluminium Inorganic materials 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- 239000004642 Polyimide Substances 0.000 description 5
- 229910052742 iron Inorganic materials 0.000 description 5
- 238000005461 lubrication Methods 0.000 description 5
- 229920001721 polyimide Polymers 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 238000002485 combustion reaction Methods 0.000 description 4
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- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- -1 polyphenylene Polymers 0.000 description 4
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 3
- DSVRVHYFPPQFTI-UHFFFAOYSA-N bis(ethenyl)-methyl-trimethylsilyloxysilane;platinum Chemical compound [Pt].C[Si](C)(C)O[Si](C)(C=C)C=C DSVRVHYFPPQFTI-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 239000003575 carbonaceous material Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000011247 coating layer Substances 0.000 description 3
- 238000010304 firing Methods 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 238000007747 plating Methods 0.000 description 3
- 229910052582 BN Inorganic materials 0.000 description 2
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 230000002159 abnormal effect Effects 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
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- 239000007788 liquid Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 2
- 229910010271 silicon carbide Inorganic materials 0.000 description 2
- MEJYDZQQVZJMPP-ULAWRXDQSA-N (3s,3ar,6r,6ar)-3,6-dimethoxy-2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan Chemical compound CO[C@H]1CO[C@@H]2[C@H](OC)CO[C@@H]21 MEJYDZQQVZJMPP-ULAWRXDQSA-N 0.000 description 1
- ZFPGARUNNKGOBB-UHFFFAOYSA-N 1-Ethyl-2-pyrrolidinone Chemical compound CCN1CCCC1=O ZFPGARUNNKGOBB-UHFFFAOYSA-N 0.000 description 1
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 1
- NRYXPBBYSDBIJO-UHFFFAOYSA-N 3,3,3-triethoxypropan-1-amine Chemical compound CCOC(CCN)(OCC)OCC NRYXPBBYSDBIJO-UHFFFAOYSA-N 0.000 description 1
- CNODSORTHKVDEM-UHFFFAOYSA-N 4-trimethoxysilylaniline Chemical group CO[Si](OC)(OC)C1=CC=C(N)C=C1 CNODSORTHKVDEM-UHFFFAOYSA-N 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- XMWRBQBLMFGWIX-UHFFFAOYSA-N C60 fullerene Chemical compound C12=C3C(C4=C56)=C7C8=C5C5=C9C%10=C6C6=C4C1=C1C4=C6C6=C%10C%10=C9C9=C%11C5=C8C5=C8C7=C3C3=C7C2=C1C1=C2C4=C6C4=C%10C6=C9C9=C%11C5=C5C8=C3C3=C7C1=C1C2=C4C6=C2C9=C5C3=C12 XMWRBQBLMFGWIX-UHFFFAOYSA-N 0.000 description 1
- CTHHHRUXSHSHOF-UHFFFAOYSA-N CO[Si](CCCNCCN)(OC)OCCCCNCCN Chemical compound CO[Si](CCCNCCN)(OC)OCCCCNCCN CTHHHRUXSHSHOF-UHFFFAOYSA-N 0.000 description 1
- 229910004261 CaF 2 Inorganic materials 0.000 description 1
- 101150065749 Churc1 gene Proteins 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- 229910000861 Mg alloy Inorganic materials 0.000 description 1
- 229920000265 Polyparaphenylene Polymers 0.000 description 1
- 102100038239 Protein Churchill Human genes 0.000 description 1
- 229910010413 TiO 2 Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000000573 anti-seizure effect Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910021393 carbon nanotube Inorganic materials 0.000 description 1
- 239000002041 carbon nanotube Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 230000007123 defense Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 229910003472 fullerene Inorganic materials 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- LQBJWKCYZGMFEV-UHFFFAOYSA-N lead tin Chemical compound [Sn].[Pb] LQBJWKCYZGMFEV-UHFFFAOYSA-N 0.000 description 1
- HZZOEADXZLYIHG-UHFFFAOYSA-N magnesiomagnesium Chemical compound [Mg][Mg] HZZOEADXZLYIHG-UHFFFAOYSA-N 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- GJVFBWCTGUSGDD-UHFFFAOYSA-L pentamethonium bromide Chemical compound [Br-].[Br-].C[N+](C)(C)CCCCC[N+](C)(C)C GJVFBWCTGUSGDD-UHFFFAOYSA-L 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- 229920001643 poly(ether ketone) Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000012791 sliding layer Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- UBMUZYGBAGFCDF-UHFFFAOYSA-N trimethoxy(2-phenylethyl)silane Chemical compound CO[Si](OC)(OC)CCC1=CC=CC=C1 UBMUZYGBAGFCDF-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D179/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen, with or without oxygen, or carbon only, not provided for in groups C09D161/00 - C09D177/00
- C09D179/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
- C09D179/08—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
-
- 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
- B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
- B05D3/02—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by baking
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
-
- C09D7/12—
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Lubricants (AREA)
- Paints Or Removers (AREA)
Abstract
본 발명은 접동부재용 코팅 조성물 및 이를 이용한 접동부재 코팅방법에 관한 것이다.
PAI(polyamide imide), PTFE, 탄소섬유, 그래핀 분말, 테트라포드 산화아연(Tetrapod ZnO), 실란커플링제, 유기용매, 소포제 및 분산제가 중량비에 의해 일정 비율로 혼합되는 윤활부재용 코팅 슬러리 조성물을 이용한 접동부재용 코팅 슬러리의 제조 및 코팅방법에 있어서, 윤활부재용 코팅 슬러리 조성물의 점도를 30~40cP인 범위로 조정하는 단계와, 플라스틱이나 세라믹제품의 원통형 용기에 넣어 상온에서 1~2시간 동안 밀링하여 코팅 슬러리를 제조하는 단계와, 코팅 슬러리의 표면조도를 1~2㎛정도로 거칠게 처리한 기재의 표면을 탈지, 세척하는 단계와, 스프레이, 롤링, 브러싱, 옵셋 및 스크린 인쇄 중 어느 하나의 방법으로 0~30㎛ 두께로 접동부재에 코팅하는 단계와, 80~100℃에서 30~60분간 건조하는 단계 및 200~250℃에서 1~2시간 소성한 후, 서서히 실온으로 냉각하는 단계를 포함한다.The present invention relates to a coating composition for sliding parts and a sliding member coating method using the same.
A coating slurry composition for a lubricant member in which PAI (polyamide imide), PTFE, carbon fiber, graphene powder, Tetrapod ZnO, silane coupling agent, organic solvent, antifoaming agent and dispersant are mixed at a certain ratio by weight ratio A method for preparing a coating slurry for a sliding part, comprising the steps of: adjusting the viscosity of a coating slurry composition for a lubricating member to a range of 30 to 40 cP; placing the slurry composition in a cylindrical container of plastic or ceramic product for 1 to 2 hours at room temperature; A step of preparing a coating slurry, a step of degreasing and washing the surface of the substrate roughly treated to a surface roughness of about 1 to 2 탆, and a step of spraying, rolling, brushing, offset and screen printing Coating the slidable member with a thickness of 0 to 30 μm, drying at 80 to 100 ° C. for 30 to 60 minutes, calcining at 200 to 250 ° C. for 1 to 2 hours, It includes the steps:
Description
본 발명은 접동부재용 코팅 조성물 및 이를 이용한 접동부재 코팅방법에 관한 것이다. 더욱 상세하게는 내마모성 및 윤활성이 우수한 코팅 조성물과 이 조성물의 제조방법 및 이를 기재에 코팅하는 방법에 관한 것으로서, 철계(철 혹은 철합금), 알루미늄계(알루미늄 혹은 알루미늄 합금) 및 마그네슘계(마그네슘 혹은 마그네슘 합금) 등의 금속기재에 내마모성, 내소착성, 내열성 및 윤활성이 우수한 표면 처리를 위한 접동부재용 코팅 조성물 및 이를 이용한 접동부재 코팅방법에 관한 것이다.
The present invention relates to a coating composition for sliding parts and a sliding member coating method using the same. More particularly, the present invention relates to a coating composition excellent in abrasion resistance and lubricity, a method of producing the composition and a method of coating the substrate, and more particularly, to a method of coating an iron (iron or iron alloy), an aluminum (aluminum or aluminum alloy), and a magnesium Magnesium alloy), which is excellent in abrasion resistance, resistance to seizure, heat resistance and lubricity, and a sliding member coating method using the same.
최근에 이르러 점차 내연기관의 배기가스 규제와 연비향상이 요구되고 있으며 일반적으로 연비향상 대책으로는 재료 변화에 의한 경량화, 소량화, 고출력화 등과 더불어 접동부재의 마찰계수를 저감하기 위한 연구가 활발히 진행되고 있다.Recently, there have been increasing demands for regulation of exhaust gas of an internal combustion engine and improvement of fuel efficiency. In general, as measures for improving fuel efficiency, studies for reducing friction coefficient of a sliding member have been actively carried out in addition to weight reduction, .
특히, 사판식 공기압축기의 사판이나 내연기관의 실린다 보아 및 피스톤 스커트 부위의 윤활성 및 내마모성을 부여하는 수지 코팅 막을 형성하는 접동부재에 대한 지속적인 연구가 이루어지고 있다.Particularly, continuous research is being conducted on a swash plate of a swash plate air compressor, a cylinder bore of an internal combustion engine, and a sliding member that forms a resin coating film that imparts lubricity and wear resistance to a piston skirt.
일 예로, 일본공개특허 특개평8-199327(1986. 8. 6.)에는 사판식 압축기의 사판과 슈 사이의 소착을 방지하기 위하여 사판의 금속기재와 수지 윤활피막 사이에 동이나 알루미늄계의 재료를 용사하여 이 금속 용사 층에 납 도금, 주석도금, 납-주석도금, PTFE 피복, MoS2 또는 MoS2-흑연 혼합 층을 피복한 것이 개시되어 있다.For example, in Japanese Unexamined Patent Application Publication No. 8-199327 (Aug. 6, 1986), in order to prevent the swash plate and the shoe between the swash plate compressor and the shoe from sticking, a copper or aluminum material Tin plating, lead-tin plating, PTFE coating, MoS 2 or MoS 2 -graphite mixed layer is coated on the metal sprayed layer.
또한, 일본공개특허 특개2002-089437(2002. 3. 27.)에는 용사 층의 형성은 비용 상승이나 평면정도가 낮아지는 결점이 있어 PTFE를 함유하는 고체윤활제를 열경화수지인 폴리아미드이미드에 고착한 접동 층을 가지는 사판에 대하여 접동 하는 슈의 표면에 니켈도금을 설치하여 사판과 슈와의 윤활성을 높여 소착을 방지하는 방법도 제안되고 있으며, 일본공개특허 특개2011-213761(2011. 10. 27.)에는 결합제 수지로 폴리아미드이미드 수지와 고체윤활제 및 유기용매를 적당한 비율로 함유하는 접동부재에 대하여 제안되고 있다. In addition, Japanese Patent Application Laid-Open No. 2002-089437 (Feb. 27, 2002) discloses that the formation of the sprayed layer has a drawback that the cost is increased or the flatness is lowered, and the solid lubricant containing PTFE is fixed to the thermosetting polyamideimide There has been proposed a method in which nickel plating is provided on the surface of a sliding shoe with respect to a swash plate having a sliding layer to increase the lubricity of the swash plate and shoe to prevent the sliding therebetween. Also, Japanese Patent Application Laid- ) Discloses a sliding member containing a polyamideimide resin as a binder resin, a solid lubricant and an organic solvent in an appropriate ratio.
그리고, 일본공개특허 특개2013-209960(2013. 10. 10)에는 내연기관의 피스톤 가이드부의 접동부재 표면에 대한 윤활피막의 도포공정 중에 수지조성물의 고형화를 방지하기 위하여 결합재(수지), 고체윤활제 및 유기용매를 함유하는 윤활피막 형성용 코팅조성물에 있어서 폴리아미드 이미드수지의 평균분자량을 10000~50000으로 조정한 것을 사용하고 용제로 N-에틸-2-피로리돈을 사용한 접동부재에 대하여 제안하고 있으나, 다른 고체윤활제나 기타 기능성 첨가제에 대한 구척적인 언급은 결여되어 있다. Japanese Unexamined Patent Application Publication No. 2013-209960 (Oct. 10, 2013) discloses a method for preventing the solidification of the resin composition during the coating process of the lubricant film on the sliding member surface of the piston guide portion of the internal combustion engine, A sliding member using an N-ethyl-2-pyrrolidone as a solvent is proposed in which a polyamide imide resin having an average molecular weight adjusted to 10,000 to 50,000 in a coating composition for forming a lubricant film containing an organic solvent is proposed , There is no roundabout reference to other solid lubricants or other functional additives.
그러나 전술한 특허문헌들에 따르면, 바인더수지와 기재와의 밀착성, 바인더수지와 고체윤활제, 기능성(내마모성, 전화방지, 열전도성 등)재료 등의 적절한 종류 및 선정이나, 혼합방식이나 정밀한 분산효과 및 코팅방법 등에 관하여 구체적으로 규명한 내용이 미흡하여 이에 관한 보다 정밀한 데이터가 요구되고 있는 실정이다.However, according to the above-mentioned patent documents, it is possible to provide a binder resin and a base material, a binder resin and a solid lubricant, a suitable type and selection of materials (wear resistance, anti-telephone, Coating method and the like are insufficient, so that more accurate data is required.
한편, 접동부재를 기재의 표면에 코팅하는 작업에 있어서는 고체윤활제의 조성물에 대한 구성비와 함께 유기용매의 종류 및 그 첨가량에 따른 고형분 함량 및 슬러리의 점성 변화 등에 따라 윤활부재의 내마모성, 기재와의 밀착성, 내열성, 내구성, 내소착성 및 윤활성 등의 제반 물리화학적인 특성에 영향을 미치는 것으로 알려져 있다. On the other hand, in the operation of coating the sliding member on the surface of the base material, the abrasion resistance of the lubricating member, the adhesiveness with the base material, and the like are affected by the composition ratio of the solid lubricant to the composition and the solid content depending on the kind of the organic solvent, , Heat resistance, durability, resistance to seizure and lubrication, and the like.
이에 따라 코팅 조성물의 점도나 분산 특성에 따라 균일하고 얇은 코팅 층을 얻기 위한 접동부재 조성물 중의 바인더수지, 고체윤활제, 기타 기능성 재료인 가교제, 커플링제, 레벨링제, 내마모재, 및 유기용매의 종류와 그 사용량 등에 관한 정밀한 조정이 요구된다.
Accordingly, it is possible to provide a binder resin, a solid lubricant, a crosslinking agent, a coupling agent, a leveling agent, an abrasion resistant material, and an organic solvent in a sliding member composition for obtaining a uniform and thin coating layer according to the viscosity or dispersion characteristics of the coating composition And the amount of use thereof.
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이와 같은 문제점을 해결하기 위하여 본 발명은 전술한 배경기술에 의해서 안출된 것으로, 윤활부재의 내마모성, 기재와의 밀착성, 내열성, 내구성, 내소착성 및 윤활성 등의 제반 물리화학적인 특성이 우수한 코팅 조성물과 이 코팅 조성물의 구성비에 따른 코팅 슬러리의 제조방법과 기재에 대한 코팅방법을 제공하는 데 그 목적이 있다. DISCLOSURE OF THE INVENTION The present invention has been made in view of the above circumstances and provides a coating composition having excellent physical and chemical properties such as abrasion resistance, And a coating method for a substrate according to the composition ratio of the coating composition.
또한 본 발명은 접동부재용 코팅 슬러리를 조제하여 일정한 피막의 두께로 기재에 도포한 후 대기압 분위기 하에서 가열하고, 건조 및 소성하여 도포 층의 용매 잔량이 약 0.1% 이하로 되게 조정한 코팅방법을 제공하는 것을 목적으로 한다.
Also, the present invention provides a coating method in which a coating slurry for a sliding part is prepared and applied to a substrate with a predetermined coating thickness, heated under atmospheric pressure, dried, and fired to adjust the residual solvent amount of the coating layer to about 0.1% or less .
이와 같은 과제를 달성하기 위한 본 발명의 일 실시예에 따르면, 바인더 수지로 열경화성 수지인 폴리아미드이미드(polyamide imide) 및 폴리이미드(polyimide)를 사용하고, 고체 윤활제는 PTFE, MoS2, 탄소섬유, 그래핀 나노플레이트 분말과, 기능성 첨가제인 테트라포드 산화아연(T-ZnO)분말, 실란커플링제, 플라티늄디비닐테트라메틸디실록산, 소포제와 분산제, 및 유기용매로 NMP, DMAC, MEK, 및 Xylene을 사용하는 윤활부재용 코팅 슬러리 조성물을 포함하고, 상기 윤활부재용 코팅 슬러리 조성물은 중량%로 바인더 수지인 PAI(polyamide imide)의 첨가량은 30~55중량%, 고체윤활제인 PTFE의 첨가량은 10~25중량%이고, 탄소섬유는 0.5~2.0중량%, 그래핀 분말 0.2~1.5중량%, 기능성 금속산화물인 테트라포드 산화아연(Tetrapod ZnO) 0.2~1.5중량%, 및 실란커플링제 0.1~1.0중량%, 유기용매로는 NMP는 10~22중량%이며, 자일렌, 또는 크실렌 중 어느 하나 10~15중량% 및 DMAC는 2~6중량%, MEK 2~6중량%로 구성되며, 이외에 소포제 및 분산제가 0.01~0.1중량% 더 첨가되는 것을 특징으로 한다.According to an embodiment of the present invention, a thermosetting resin such as polyamide imide and polyimide is used as the binder resin, and a solid lubricant includes PTFE, MoS 2 , A carbon fiber, a graphene nanoplate powder, a functional additive T-ZnO powder, a silane coupling agent, a platinum divinyl tetramethyldisiloxane, a defoaming agent and a dispersant, and an organic solvent such as NMP, DMAC, MEK, Xylene, wherein the amount of the binder resin PAI (polyamide imide) is 30 to 55 wt%, the amount of the PTFE as a solid lubricant is 10 And 0.2 to 1.5 wt% of carbon fiber, 0.2 to 1.5 wt% of graphene powder, 0.2 to 1.5 wt% of tetrapod ZnO as a functional metal oxide, and 0.1 to 1.0 wt% of a silane coupling agent, , 10 to 22% by weight of NMP as an organic solvent, 10 to 15% by weight of any one of xylene and xylene, 2 to 6% by weight of DMAC and 2 to 6% by weight of MEK, Is added in an amount of 0.01 to 0.1% by weight.
본 발명의 일 실시예에 따르면, 상기 윤활부재용 코팅 슬러리 조성물은 코팅액 조성물의 점도가 30~40cP가를 이루도록 구성되는 것을 특징으로 한다.According to an embodiment of the present invention, the coating slurry composition for a lubricant member is characterized in that the viscosity of the coating liquid composition is 30 to 40 cP.
본 발명의 일 실시예에 따르면, 상기 PTFE의 입도는 0.15~5.0㎛, MoS2는 0.5~0.7㎛인 것을 사용하는 것을 특징으로 한다.According to an embodiment of the present invention, the particle size of the PTFE is 0.15-5.0 탆 and the MoS 2 is 0.5-0.7 탆.
본 발명의 일 실시예에 따르면, 상기 테트라포드 산화아연(tetrapod ZnO)은 평균 길이 10.0㎛ 이하, 직경 50~100nm인 것을 사용하는 것을 특징으로 한다.According to an embodiment of the present invention, the tetrapod ZnO has an average length of 10.0 탆 or less and a diameter of 50-100 nm.
본 발명의 일 실시예에 따르면, 상기 탄소섬유는 직경 5㎛, 길이10㎛ 이하, 그래핀 나노플레이트 분말은 50~500nm인 것을 사용하는 것을 특징으로 한다.According to an embodiment of the present invention, the carbon fiber has a diameter of 5 탆, a length of 10 탆 or less, and a graphene nanoplate powder of 50 to 500 nm.
본 발명의 일 실시예에 따르면, PAI(polyamide imide), PTFE, 탄소섬유, 그래핀 분말, 테트라포드 산화아연(Tetrapod ZnO), 실란커플링제, 유기용매, 소포제 및 분산제가 중량비에 의해 일정 비율로 혼합되는 윤활부재용 코팅 슬러리 조성물을 이용한 접동부재용 코팅 슬러리의 제조 및 코팅방법에 있어서, (a) 상기 윤활부재용 코팅 슬러리 조성물의 점도를 30~40cP인 범위로 조정하는 단계; (b) 플라스틱이나 세라믹제품의 원통형 용기에 넣어 상온에서 1~2시간 동안 밀링하여 코팅 슬러리를 제조하는 단계; (c) 상기 코팅 슬러리의 표면조도를 1~2㎛정도로 거칠게 처리한 기재의 표면을 탈지, 세척하는 단계; (d) 스프레이, 롤링, 브러싱, 옵셋 및 스크린 인쇄 중 어느 하나의 방법으로 0~30㎛ 두께로 상기 접동부재에 코팅하는 단계; (e) 상기 (d) 단계 완료 후, 80~100℃에서 30~60분간 건조하는 단계; (f) 상기 (e) 단계 완료 후, 200~250℃에서 1~2시간 소성한 후, 서서히 실온으로 냉각하는 단계를 포함하는 것을 특징으로 한다.According to one embodiment of the present invention, a polyamide imide (PAI), PTFE, carbon fiber, graphene powder, Tetrapod ZnO, silane coupling agent, organic solvent, antifoaming agent, (A) adjusting the viscosity of the coating slurry composition for the lubricating member to a range of 30 to 40 cP; and (c) adjusting the viscosity of the coating slurry composition to a range of 30 to 40 cP. (b) milling in a cylindrical container of plastic or ceramic product at room temperature for 1 to 2 hours to prepare a coating slurry; (c) degreasing and washing the surface of the substrate which has been roughly treated with the surface roughness of the coating slurry to about 1 to 2 탆; (d) coating the sliding member to a thickness of 0 to 30 mu m by any one of spraying, rolling, brushing, offset, and screen printing; (e) after completion of the step (d), drying at 80 to 100 ° C for 30 to 60 minutes; (f) after completion of the step (e), firing at 200 to 250 ° C for 1 to 2 hours, and then slowly cooling to room temperature.
이와 같은 본 발명의 실시예에 따르면, 철, 알루미늄 및 마그네슘계 기재의 표면 코팅용 접동부재용 코팅 슬러리는 바인더 수지, 고체윤활제, 유기용매, 및 기타 기능성 첨가제의 종류 및 첨가량, 슬러리 상태인 코팅재의 점성의 변화에 따라 건조 및 소성공정에서 기재 표면에 대한 밀착성과 윤활성, 내마모성 등에 큰 영향을 미치는 효과를 나타낸다. According to the embodiment of the present invention, the coating slurry for a sliding part for surface coating of iron, aluminum and magnesium based materials can be suitably selected from the kinds and amounts of the binder resin, solid lubricant, organic solvent and other functional additives, It exhibits an effect of adversely affecting adhesion to the substrate surface, lubricity, abrasion resistance, etc. in the drying and firing process depending on the viscosity change.
따라서 사판식 공기압축기의 사판, 내연기관의 실린다 보아 및 피스톤 스커트 부위의 윤활제 등으로 활용이 가능하다.
Therefore, it can be used as a swash plate of a swash plate type air compressor, a cylinder bore of an internal combustion engine, and a lubricant at a piston skirt portion.
도 1은 본 발명의 일 실시예에 따른 접동부재용 코팅 슬러리 조성물의 구성비에 대한 실시예와 이를 코팅한 기재 표면의 윤활특성을 조사한 결과를 나타낸 표이다.BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a table showing results of examining the composition ratios of the coating slurry composition for a sliding part according to an embodiment of the present invention and the lubricating properties of the surface of the coated substrate. FIG.
이하, 본 발명의 바람직한 실시예를 첨부된 도면들을 참조하여 상세히 설명한다. 우선 각 도면의 구성요소들에 참조 부호를 부가함에 있어서, 동일한 구성요소들에 대해서는 비록 다른 도면상에 표시되더라도 가능한 동일한 부호를 가지도록 하고 있음에 유의해야 한다. 또한, 본 발명을 설명함에 있어, 관련된 공지 구성 또는 기능에 대한 구체적인 설명이 본 발명의 요지를 흐릴 수 있다고 판단되는 경우에는 그 상세한 설명은 생략한다. Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the accompanying drawings. In the drawings, the same reference numerals are used to designate the same or similar components throughout the drawings. In the following description of the present invention, a detailed description of known functions and configurations incorporated herein will be omitted when it may make the subject matter of the present invention rather unclear.
본 발명의 접동부재용 코팅 슬러리 조성물은 열경화성 바인더 수지, 고체윤활제, 기능성 첨가제, 실란커플링제, 소포제 및 다양한 종류의 유기용매로 구성된다. The coating slurry composition of the present invention comprises a thermosetting binder resin, a solid lubricant, a functional additive, a silane coupling agent, a defoaming agent, and various kinds of organic solvents.
바인더 수지로 열경화성 및 열가소성 수지인 폴이아미드이미드(PAI), 폴리이미드(PI), 에폭시수지(epoxy), 폴리에텔에텔케톤수지(PEEK), 폴리페닐렌수지(PPS) 등을 사용 할 수 있고, 고체 윤활제로 PTFE, MoS2, WS2, h-BN(질화붕소), 및 탄소계 소재로 흑연, 탄소나노튜브, 플러렌, 탄소섬유, 그래핀 나노플레이트 분말 등을 사용하며, 기타 기능성 첨가제로 탄화규소((SiC), 알루미나(Al2O3), 산화지르콘(ZrO2), 산화티탄(TiO2), 불화칼슘(CaF2), 테트라포드 산화아연(Tetrapod-ZnO) 등의 미분말을 사용 할 수 있다. 크로스링크제는 멜라민(melamine, C3H6N6), 실란커플링제는 아미노페닐트리메톡시실란aminophenyltrimethoxysilane, C9H15NO3Si, 아미노에틸아미노프로필특리메톡시실란N-(2-aminoethyl)-3-aminopropyltrimethoxysilane, C8H22N2O3Si, 트리에톡실프로필아민bis(triethoxypropyl)amine, C18H43NO6Si2, 크로로메틸페닐에틸트리메톡시실란chloromethyl)phenylethyltrimethoxysilane, C12H19ClO3Si, 플라디늄디비닐테트라메틸디실록산Pt(0)-1,3- divinyl-1,1,3,3- tetramethyldisiloxane를 사용 할 수 있으며, 유기용매로는 비점이 서로 다른 메틸피로리돈(NMP, N-methyl-2-pyrrolidon, C5H9NO), 디메칠아세트아마이드(DMAC, dimethylacetamide, C4H9NO), 메틸아이소부틸케톤MIBK,methylisobutyl ketone, (CH3)2CHCH2C(O)CH3, 메틸에틸케톤MEK, methyl ethyl ketone, CH3C(O)OH2CH3, 감마부티로락톤(GBL, -butylolacton, C4H6O2), 디메틸아이소소르바이드(DMI, dimethyl isosorbide, C8H14O4), 크실렌Xylene, C6H4(CH3)2 등을 사용 할 수 있다. 이외에 소포제 및 분산제를 소량 첨가할 수도 있다. (PAI), polyimide (PI), epoxy resin, polyetherketone resin (PEEK), polyphenylene resin (PPS), or the like, which is a thermosetting and thermoplastic resin, can be used as the binder resin , PTFE as a solid lubricant, MoS 2 , Graphite, carbon nanotubes, fullerene, carbon fiber, and graphene nanoplate powders are used as WS 2 , h-BN (boron nitride), and carbon-based materials. Other functional additives include silicon carbide ((SiC), alumina Fine powder such as Al 2 O 3 , ZrO 2 , TiO 2 , CaF 2 and tetrapod-ZnO can be used. melamine, C 3 H 6 N 6 ), the silane coupling agent is aminophenyltrimethoxysilane, C 9 H 15 NO 3 Si, aminoethylaminopropyl-N- (2-aminoethyl) -3-aminopropyltrimethoxysilane, C 8 H 22 N 2 O 3 Si, triethoxypropylamine, C 18 H 43 NO 6 Si 2 , chromomethylphenylethyltrimethoxysilane chloromethyl) phenylethyltrimethoxysilane, C 12 H 19 ClO 3 Si, Platinum di vinyltetramethyldisiloxane Pt (0) -1,3-divinyl-1,1,3,3-tetramethyldisiloxane can be used, and organic Sheets are pyrrolidone fatigue boiling point different methyl (NMP, N-methyl-2 -pyrrolidon, C 5 H 9 NO), di-methyl acetamide (DMAC, dimethylacetamide, C 4 H 9 NO), methyl isobutyl ketone MIBK, methylisobutyl ketone, (CH 3) 2 CHCH 2 C (O)
특히 본 발명에서는 바인더 수지로 폴리아미드이미드(PAI) 또는 폴리이미드(PI)를 사용할 수 있고, 고체윤활제로는 PTFE, MoS2, 탄소계 재료로 탄소섬유, 그래핀 나노플레이트 분말, 기능성 첨가제로 테트라포드 산화아연(Tetrapod-ZnO), 실란커플링제로 플라티늄디비닐테트라메틸디실록산, 및 소량의 소포제를 사용할 수 있으며, 유기용매로는 비점이 서로 다른 NMP, DMAC, MEK, 및 Xylene. 등을 사용하여 코팅 조성물 슬러리의 점도를 조절할 수 있다.In particular, the present invention can be used for a polyamide-imide (PAI), or polyimide (PI) of a binder resin, a solid lubricant to the PTFE, MoS 2, a carbon-based material of carbon fiber, graphene nano plate powder, teteurapodeu a functional additive Zinc oxide (Tetrapod-ZnO), silane coupling agent, platinum divinyltetramethyldisiloxane, and a small amount of antifoaming agent can be used. As the organic solvent, NMP, DMAC, MEK, and Xylene having different boiling points can be used. May be used to control the viscosity of the coating composition slurry.
상기 그래핀 나노플레이트는 전기전도성, 열전도성, 내스크레치 및 내마모성, 부식방지, 내생체오염성 등의 물성이 우수하여 우주항공, 자동차, 건설, 선박, 방위산업 분야에 활용되는 재료이다. The graphene nanoplate has excellent physical properties such as electrical conductivity, thermal conductivity, scratch resistance and abrasion resistance, corrosion resistance, and bio-stain resistance, and is used in aerospace, automobile, construction, ship and defense industries.
기능성 첨가제인 테트라포드 산화아연(Tetrapod-ZnO)은 전화방지(electrification prevention), 초발수성, 전파 및 자외선 흡수성, 열전도성, 내마모성, 항균성, 부착력 등이 우수한 재료로 수지 화합물의 필러재료로 각광을 받고 있다.Tetrapod-ZnO, a functional additive, is a material that is excellent in electrification prevention, super water repellency, propagation and ultraviolet ray absorbing property, thermal conductivity, abrasion resistance, antibacterial property and adhesion force and is attracting attention as a filler material of a resin compound .
이와 같은 본 발명의 윤활부재용 코팅 슬러리 조성물의 구성비는 바인더수지 45~55중량%, 고체윤활제(PTFE, MoS2, 탄소계 재료) 10~15중량%와 유기용매 30~35중량%, 실란커플링제 0.1~0.7중량%, 소포제 0.01~0.05중량%이고, 점도는 30~40 cP로 조정하는 것을 특징으로 한다.The composition ratio of the coating slurry composition for a lubricant of the present invention is 45 to 55% by weight of a binder resin, 10 to 15% by weight of a solid lubricant (PTFE, MoS 2 , carbonaceous material), 30 to 35% by weight of an organic solvent, 0.1 to 0.7% by weight of a lubricant, 0.01 to 0.05% by weight of an antifoam agent, and a viscosity of 30 to 40 cP.
또한, 보다 자세한 윤활부재용 코팅 슬러리 조성물의 구성비는 전체 조성물의 중량%로 PAI 40~55중량%, 고체윤활제 PTFE 5~15중량%, MoS2 5~10중량%이며, 가장 적합한 비율은 8~10중량% 이다. 테트라포드 산화아연(tetrapod ZnO2) 0.1~1.0중량%, 실란커플링제 0.1~1.0중량%이며, 최적 적합 첨가량은 0.5~1.0중량%이다. 이외에 레벨링제 및 소포제 등은 약 0.01~0.1중량% 첨가할 수 있다.Further, the composition ratio of the coating slurry composition for the lubricant member is 40 to 55% by weight of PAI, 5 to 15% by weight of solid lubricant PTFE and 5 to 10% by weight of MoS 2 , 10% by weight. 0.1 to 1.0% by weight of tetrapod ZnO 2 , 0.1 to 1.0% by weight of a silane coupling agent, and an optimum amount of added is 0.5 to 1.0% by weight. In addition, about 0.01 to 0.1% by weight of a leveling agent and a defoaming agent may be added.
유기용매로는 NMP 10~22중량%, 가장 적합한 량은 12~17중량%, 크실렌은 9~15중량%, 최적량은 8~10중량%, DMAC 및 MEK는 2~6중량%, 최적량은 3~5중량%로 조정하여 전체 코팅액 조성물의 점도가 30~40cP가 되도록 조절하는 것을 특징으로 한다. As the organic solvent, 10 to 22 wt% of NMP, 12 to 17 wt% of the most suitable amount, 9 to 15 wt% of xylene, 8 to 10 wt% of optimal amount, 2 to 6 wt% of DMAC and MEK, Is adjusted to 3 to 5% by weight so that the viscosity of the entire coating liquid composition is adjusted to be 30 to 40 cP.
즉, 본 발명의 접동부재용 코팅 슬러리의 최적의 조성물은 중량%로 바인더 수지인 PAI의 첨가량은 30~55중량%, 고체윤활제인 PTFE의 첨가량은 10~25중량%이고, 탄소섬유는 0.5~2.0중량%, 그래핀 분말 0.2~1.5중량%, 기능성 금속산화물인 테트라포드 산화아연(Tetrapod ZnO) 0.2~1.5중량%, 및 실란커플링제 0.1~1.0중량%, 유기용매로는 NMP는 10~22중량%이며, 자일렌, 또는 크실렌 중 어느 하나 10~15중량% 및 DMAC는 2~6중량%, MEK 2~6중량%로 구성되며, 이외에 소포제 및 분산제가 0.01~0.1중량% 첨가되어 코팅액 조성물의 점도가 30~40cP가를 이루도록 구성되는 것이다.That is, the optimum composition of the coating slurry for a sliding part of the present invention is 30 to 55 wt% of PAI as a binder resin, 10 to 25 wt% of a PTFE as a solid lubricant, 0.2 to 1.5% by weight of zinc oxide (Tetrapod ZnO), 0.1 to 1.0% by weight of a silane coupling agent, and 10 to 22% by weight of an organic solvent And 10 to 15% by weight of any one of xylene and xylene, 2 to 6% by weight of DMAC and 2 to 6% by weight of MEK, 0.01 to 0.1% by weight of a defoaming agent and a dispersant are added, And a viscosity of 30 to 40 cP.
상기한 조성물의 구성비가 부족하거나 초과하는 경우에는 바인더 수지의 경우, 기재와의 밀착성의 감소현상이나 상대적으로 윤활제 또는 기타 첨가제의 성능저하 현상을 나타낸다. When the composition ratio of the above-mentioned composition is insufficient or exceeds the above-mentioned range, the binder resin exhibits a decrease in adhesion with the base material and a decrease in performance of the lubricant or other additives.
또한, 고체윤활제 및 기능성 첨가제의 경우, 코팅 층의 윤활성, 내열성, 내소착성 등의 물성의 저하현상이나 과도한 사용으로 인한 비용 문제 등이 발생 할 염려가 있다. In addition, in the case of the solid lubricant and the functional additive, the physical properties such as lubricity, heat resistance, and anti-seizure property of the coating layer may be deteriorated and cost problems due to excessive use may occur.
용매의 경우에는 비점이 서로 상이한 용매를 적당히 조절하여 코팅 슬러리의 점도를 최적으로 조정할 필요가 있으므로 용매의 과부족 현상이나 상호 혼합비율의 상이성은 코팅 슬러리의 도포에 많은 영향을 미치게 된다.In the case of a solvent, it is necessary to adjust the viscosity of the coating slurry to an optimum level by appropriately adjusting a solvent having a different boiling point, so that the difference in the ratio of the solvent over and under and the mutual mixing ratio greatly affects the application of the coating slurry.
여기서, 고체윤활제인 PTFE의 입도는 0.15~5.0㎛, MoS2는 0.5~0.7㎛인 것을 사용하고, 테트라포드 산화아연(tetrapod ZnO)은 평균 길이 약 10.0㎛ 이하, 직경 50~100nm, 탄소섬유는 직경 5㎛, 길이10㎛이하, 그리고 그래핀 나노플레이트 분말은 50~500nm인 것을 사용한다.Here, the particle size of the solid lubricant PTFE is 0.15 to 5.0 mu m and the MoS 2 is 0.5 to 0.7 mu m. The tetrapod ZnO has an average length of about 10.0 mu m or less, a diameter of 50 to 100 nm, 5 mu m, a length of 10 mu m or less, and a graphene nanoplate powder of 50 to 500 nm.
아울러, 기재에 대한 코팅 슬러리의 제조 및 코팅방법은 바인더 수지 PAI, 고체윤활제 PTFE, MoS2, 탄소섬유, 그래핀 분말, 기능성 첨가제인 테트하포드 산화아연(tetrapod ZnO), Pt-silane(플라티늄디비닐테트라메틸디실록산), NMP( N-Methyl pyrrolidone), 자일렌(Xylene), 크실렌, DMAC(Dimethylacetamide), MEK를 포함하는 용매 등을 상기한 구성비로 혼합하여 슬러리의 점도를 조정한다. In addition, methods for making and coating coating slurries on substrates include but are not limited to binder resin PAI, solid lubricant PTFE, MoS 2 , carbon fibers, graphene powder, tetrapod ZnO, a functional additive, A solvent including NMP (N-methyl pyrrolidone), xylene, xylene, DMAC (Dimethylacetamide), and MEK is mixed in the above ratio to adjust the viscosity of the slurry.
그리고, 플라스틱이나 세라믹제품의 원통형 용기에 넣어 상온에서 약 1~2시간 밀링하여 코팅 슬러리를 제조한다. Then, it is put into a cylindrical container made of plastic or ceramic product and milled at room temperature for about 1 to 2 hours to prepare a coating slurry.
상기 코팅 슬러리의 표면조도를 약 1~2㎛정도로 거칠게 처리한 기재의 표면을 탈지, 세척한 다음, 스프레이, 롤링, 브러싱, 옵셋 및 스크린 인쇄 등의 일반적인 공지의 코팅방법으로 약 10~30㎛ 두께로 코팅한 후, 80~100℃에서 30~60분간 건조시키고, 건조가 완료되면, 약 200~250℃에서 1~2시간 소성한 후, 서서히 실온으로 냉각하여 코팅작업을 수행한다. The surface of the substrate having rough surface roughness of the coating slurry of about 1 to 2 탆 is degreased and washed and then coated on the surface of the substrate by a known coating method such as spraying, rolling, brushing, offset and screen printing to a thickness of about 10 to 30 탆 And then dried at 80 to 100 ° C. for 30 to 60 minutes. When drying is completed, the coated substrate is baked at about 200 to 250 ° C. for 1 to 2 hours, and then slowly cooled to room temperature to perform a coating operation.
소성 후 코팅 표면의 연필경도는 4H 정도이다.The pencil hardness of the coated surface after firing is about 4H.
도 2는 본 발명의 접동부재용 코팅 슬러리 조성물의 종류 및 그 구성비에 대한 실시예와 이를 코팅한 기재 표면의 윤활특성을 조사한 결과를 나타낸 것이다. FIG. 2 shows the results of examining examples of the kinds and composition ratios of the coating slurry compositions for sliding parts of the present invention and the lubrication characteristics of the surface of the coated substrates.
윤활특성에 관한 시험으로는 다음과 같은 시험 과정을 거쳐 윤활특성을 측정한다.As a test for the lubrication characteristics, the lubrication characteristics are measured through the following test procedure.
ML시험은 사판에 윤활유가 공급되는 정상적 운전 상태에서 윤활유가 없는 비정상적인 상태로 임의적으로 조작하여 이 상태를 어느 정도 견디는 가를 측정하는 마모 내구성 시험이다. The ML test is a wear durability test that measures the degree of resistance to abnormal conditions in which the lubricating oil is supplied to the swash plate under normal operating conditions.
이는 제품의 사용 중에 발생 할 수 있는 최악의 조건을 가정하여 하기의 표 1의 시저(seizure) 테스트 ML기준표에서 단계 6에서 2,300rpm, 200kgf 하중의 하중의 무윤활 상태에서 10분 이상 가동되어야 기준을 통과하는 것으로 설정한다. This assumes that the worst possible conditions that may occur during use of the product are fulfilled and that the criteria should be maintained for at least 10 minutes in the no-lubrication state of the loads of 2,300rpm and 200kgf in
RL시험은 정상적 운전 상태에서 외부의 충격 또는 다른 요인에 의해 비정상적인 하중을 받을 경우 얼마만한 하중을 견딜 수 있는 가의 여부를 결정하는 내하중 시험으로, 표 2의 시저(seizure) 시험 RL기준표에서 단계 1에서 단계 3까지는 정상적인 운전 상태이고, 단계 4에서는 정상적 운전상태(1000rpm, 윤활유 공급상태)를 유지하면서 45kgf 하중에서부터 계속 하중을 증가시키는 시험으로 1,300kgf이상을 견딜 수 있어야 기준을 통과하는 것으로 규정 되어있다. The RL test is an internal load test to determine how much load can be tolerated under abnormal loads due to external shocks or other factors under normal operating conditions. The seismic load test in Table 2, Step 1 To 3 is a normal operating condition, and in
마찰계수 측정은 고온왕복운동 마찰마모시험기(Cameron Plint사 제품, ASTM G133)를 사용하여 시험하중 20kg/cm2, 미끄럼 속도 0.14m/sec(10Hz)로 설정하여 측정하였다. 시험편의 온도는 실제 기재의 온도 상승을 고려하여 150℃로 유지하였다.
The friction coefficient was measured using a high-temperature reciprocating friction and abrasion tester (Cameron Plint, ASTM G133) at a test load of 20 kg / cm 2 and a sliding speed of 0.14 m / sec (10 Hz). The temperature of the test piece was maintained at 150 캜 in consideration of the temperature rise of the actual substrate.
[표 1] 시저(seizure) 테스트 ML기준표[Table 1] Seizure test ML reference table
[표 2] 시저(seizure) 테스트 RL기준표
[Table 2] Seizure test RL reference table
도 2에 도시된 바와 같이, 실시예 1~10의 조건에서는 ML 및 RL의 시험 기준을 모두 통과하는 것을 알 수 있다. As shown in FIG. 2, it can be seen that the conditions of Examples 1 to 10 pass all of the ML and RL test standards.
즉, 윤활부재 코팅 슬러리의 고형분이 20~25중량%, 점도가 30~40cP인 범위에서 상기한 코팅 슬러리 조성물의 첨가 범위 내에서 모든 시험 기준을 만족하는 것을 알 수 있다. That is, it can be seen that all the test standards are satisfied within the range of the coating slurry composition in the range of 20 to 25% by weight of solid content of the lubricant coating slurry and the viscosity of 30 to 40 cP.
그러나 고형분(고체윤활제, 기능성 재료 등)의 종류, 첨가량 및 슬러리 조성물의 점도가 상기한 범위를 벗어나는 구성비, 즉 비교예에서는 시험규격을 만족하지 못하는 결과를 나타내고 있음을 알 수 있다. However, it can be seen that the composition ratio in which the kind of solid content (solid lubricant, functional material, etc.), the addition amount thereof, and the viscosity of the slurry composition are out of the above range, that is, the test specimen is not satisfied in the comparative example.
따라서 철계, 알루미늄계 및 마그네슘계 기재의 표면 코팅용 접동부재용 코팅 슬러리 조성은 바인더 수지, 고체윤활제, 기타 첨가제 및 유기용매의 종류 및 구성비가 매우 좁은 범위 내에서 조정되어야 규격에 적합한 제품을 제조 할 수 있음을 알 수 있다. Therefore, the coating slurry composition for sliding parts for surface coating of iron-based, aluminum-based and magnesium-based substrates should be adjusted within a very narrow range of binder resin, solid lubricant, other additive and organic solvent, .
본 발명에 관계되는 습동용 내마모성 윤활 피복 조성물은 철계, 알미늄계 및 마그네슘계 등의 표면 피복용으로써 사용된다. The abrasion-resistant lubricating coating composition for wetting according to the present invention is used for surface coating of iron-based, aluminum-based, magnesium-based and the like.
피복전의 표면처리는 알루미나(Alumina) 분말로 표면 샌딩(Sanding) 한 후 샌딩한 금속 표면을 고압 건조 에어로 이물질과 같은 더스트를 완전히 제거한 후 코팅 작업을 빠른 시간내에 실시하며 코팅 작업시 주변 공기는 건조한 공기 분위기에 약간의 불활성 가스를 함유하는 분위기가 금속피도물의 표면을 깨끗한 상태로 유지하며 도막 밀착 성능을 향상하도록 한다. Surface treatment before coating is performed by surface sanding with alumina powder, then dusting the sanded metal surface with high-pressure drying air completely, and then performing the coating operation in a short period of time. In the coating operation, An atmosphere containing a slight inert gas in the atmosphere keeps the surface of the metal substrate in a clean state and improves the coating film adhesion performance.
특히, 금속 표면의 샌딩 표면은 2~3 미크론(mRz)이 바람직하고 코팅도막은 17 mRz ~23 mRz 정도가 바람직하며, 보다 구체적으로는 20mRz가 바람직하다.In particular, the sanding surface of the metal surface is preferably 2 to 3 microns (mRz), and the coating film is preferably 17 mRz to 23 mRz, more preferably 20 mRz.
이상에서, 본 발명의 실시예를 구성하는 모든 구성 요소들이 하나로 결합되거나 결합되어 동작하는 것으로 설명되었다고 해서, 본 발명이 반드시 이러한 실시예에 한정되는 것은 아니다. 즉, 본 발명의 목적 범위 안에서라면, 그 모든 구성 요소들이 하나 이상으로 선택적으로 결합하여 동작할 수도 있다. While the present invention has been described in connection with what is presently considered to be the most practical and preferred embodiments, it is to be understood that the invention is not limited to the disclosed embodiments. That is, within the scope of the present invention, all of the components may be selectively coupled to one or more of them.
또한, 이상에서 기재된 "포함하다", "구성하다" 또는 "가지다" 등의 용어는, 특별히 반대되는 기재가 없는 한, 해당 구성 요소가 내재될 수 있음을 의미하는 것이므로, 다른 구성 요소를 제외하는 것이 아니라 다른 구성 요소를 더 포함할 수 있는 것으로 해석되어야 하며, 기술적이거나 과학적인 용어를 포함한 모든 용어들은, 다르게 정의되지 않는 한, 본 발명이 속하는 기술 분야에서 통상의 지식을 가진 자에 의해 일반적으로 이해되는 것과 동일한 의미를 가진다. It is also to be understood that the terms such as " comprises, "" comprising," or "having ", as used herein, mean that a component can be implanted unless specifically stated to the contrary. And all terms including technical and scientific terms are to be construed in a manner generally known to one of ordinary skill in the art to which this invention belongs, It has the same meaning as understood.
이상의 설명은 본 발명의 기술 사상을 예시적으로 설명한 것에 불과한 것으로서, 본 발명이 속하는 기술 분야에서 통상의 지식을 가진 자라면 본 발명의 본질적인 특성에서 벗어나지 않는 범위에서 다양한 수정 및 변형이 가능할 것이다. 따라서, 본 발명에 개시된 실시예들은 본 발명의 기술 사상을 한정하기 위한 것이 아니라 설명하기 위한 것이고, 이러한 실시예에 의하여 본 발명의 기술 사상의 범위가 한정되는 것은 아니다. 본 발명의 보호 범위는 아래의 청구범위에 의하여 해석되어야 하며, 그와 동등한 범위 내에 있는 모든 기술 사상은 본 발명의 권리범위에 포함되는 것으로 해석되어야 할 것이다.
The foregoing description is merely illustrative of the technical idea of the present invention, and various changes and modifications may be made by those skilled in the art without departing from the essential characteristics of the present invention. Therefore, the embodiments disclosed in the present invention are intended to illustrate rather than limit the scope of the present invention, and the scope of the technical idea of the present invention is not limited by these embodiments. The scope of protection of the present invention should be construed according to the following claims, and all technical ideas within the scope of equivalents should be construed as falling within the scope of the present invention.
Claims (6)
상기 윤활부재용 코팅 슬러리 조성물은
중량%로 바인더 수지인 PAI(polyamide imide)의 첨가량은 30~55중량%, 고체윤활제인 PTFE의 첨가량은 5~15중량%, MoS2은 5~10중량%, 탄소섬유는 0.5~2.0중량%, 그래핀 분말 0.2~1.5중량%, 기능성 금속산화물인 테트라포드 산화아연(Tetrapod ZnO) 0.2~1.5중량%, 및 실란커플링제 0.1~1.0중량%, 유기용매로 NMP는 10~22중량%이며, 자일렌, 또는 크실렌 중 어느 하나 10~15중량% 및 DMAC는 2~6중량%, MEK 2~6중량%로 구성되며, 이외에 소포제 및 분산제가 0.01~0.1중량% 더 첨가되는 것을 특징으로 하는 윤활부재용 코팅 슬러리 조성물.
Polyamide imide, which is a thermosetting resin, is used as the binder resin, and solid lubricants such as PTFE, MoS 2 , A coating slurry composition for a lubricating member using carbon fiber, graphene powder, T-ZnO powder as a functional additive, a silane coupling agent, a defoaming agent and a dispersant, and NMP, DMAC, MEK, and Xylene as organic solvents / RTI >
The coating slurry composition for the lubricating member
The addition amount of polyamide imide (PAI) as a binder resin is 30 to 55 wt%, the addition amount of PTFE as a solid lubricant is 5 to 15 wt%, the amount of MoS 2 is (Tetrapod ZnO) of 0.2 to 1.5% by weight, and a silane coupling agent of 0.1 to 1.0% by weight, the carbon fiber is 0.5 to 2.0% by weight, the graphene powder is 0.2 to 1.5% , 10 to 22% by weight of NMP as an organic solvent, 10 to 15% by weight of any one of xylene and xylene, 2 to 6% by weight of DMAC and 2 to 6% by weight of MEK, 0.01 to 0.1% by weight based on the total weight of the lubricant.
상기 윤활부재용 코팅 슬러리 조성물은 코팅액 조성물의 점도가 30~40cP가를 이루도록 구성되는 것을 특징으로 하는 윤활부재용 코팅 슬러리 조성물.
The method according to claim 1,
Wherein the coating slurry composition for a lubricant member is configured such that the viscosity of the coating fluid composition is from 30 to 40 cP.
상기 PTFE의 입도는 0.15~5.0㎛, MoS2는 0.5~0.7㎛인 것을 사용하는 것을 특징으로 하는 윤활부재용 코팅 슬러리 조성물.
The method according to claim 1,
Wherein the PTFE has a particle size of 0.15 to 5.0 탆 and a MoS 2 of 0.5 to 0.7 탆.
상기 테트라포드 산화아연(tetrapod ZnO)은 평균 길이 10.0㎛ 이하, 직경 50~100nm인 것을 사용하는 것을 특징으로 하는 윤활부재용 코팅 슬러리 조성물.
The method according to claim 1,
Wherein the tetrapod ZnO has an average length of 10.0 탆 or less and a diameter of 50 to 100 nm.
상기 탄소섬유는 직경 5㎛, 길이10㎛ 이하, 그래핀 나노플레이트 분말은 50~500nm인 것을 사용하는 것을 특징으로 하는 윤활부재용 코팅 슬러리 조성물.
The method according to claim 1,
Wherein the carbon fiber has a diameter of 5 탆, a length of 10 탆 or less, and a graphene nanoplate powder of 50 to 500 nm.
(a) 상기 윤활부재용 코팅 슬러리 조성물의 점도를 30~40cP인 범위로 조정하는 단계;
(b) 플라스틱이나 세라믹제품의 원통형 용기에 넣어 상온에서 1~2시간 동안 밀링하여 코팅 슬러리를 제조하는 단계;
(c) 상기 코팅 슬러리의 표면조도를 1~2㎛정도로 거칠게 처리한 기재의 표면을 탈지, 세척하는 단계;
(d) 스프레이, 롤링, 브러싱, 옵셋 및 스크린 인쇄 중 어느 하나의 방법으로 0~30㎛ 두께로 상기 접동부재에 코팅하는 단계;
(e) 상기 (d) 단계 완료 후, 80~100℃에서 30~60분간 건조하는 단계;
(f) 상기 (e) 단계 완료 후, 200~250℃에서 1~2시간 소성한 후, 서서히 실온으로 냉각하는 단계
를 포함하는 것을 특징으로 하는 접동부재용 코팅 슬러리의 제조 및 코팅방법.
A coating slurry composition for a lubricant member in which PAI (polyamide imide), PTFE, carbon fiber, graphene powder, Tetrapod ZnO, silane coupling agent, organic solvent, antifoaming agent and dispersant are mixed at a certain ratio by weight ratio A method for preparing and coating a coating slurry for a sliding part,
(a) adjusting the viscosity of the coating slurry composition for the lubricating member to a range of 30 to 40 cP;
(b) milling in a cylindrical container of plastic or ceramic product at room temperature for 1 to 2 hours to prepare a coating slurry;
(c) degreasing and washing the surface of the substrate which has been roughly treated with the surface roughness of the coating slurry to about 1 to 2 탆;
(d) coating the sliding member to a thickness of 0 to 30 mu m by any one of spraying, rolling, brushing, offset, and screen printing;
(e) after completion of the step (d), drying at 80 to 100 ° C for 30 to 60 minutes;
(f) after completion of the step (e), calcining at 200 to 250 ° C for 1 to 2 hours and then slowly cooling to room temperature
Wherein the coating slurry is coated on the substrate.
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