JPH05255571A - Composite resin composition - Google Patents
Composite resin compositionInfo
- Publication number
- JPH05255571A JPH05255571A JP7313891A JP7313891A JPH05255571A JP H05255571 A JPH05255571 A JP H05255571A JP 7313891 A JP7313891 A JP 7313891A JP 7313891 A JP7313891 A JP 7313891A JP H05255571 A JPH05255571 A JP H05255571A
- Authority
- JP
- Japan
- Prior art keywords
- resin composition
- composite resin
- zinc oxide
- composition according
- fatty acid
- 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.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims description 24
- 239000000805 composite resin Substances 0.000 title claims description 21
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims abstract description 70
- 239000011787 zinc oxide Substances 0.000 claims abstract description 35
- 239000011347 resin Substances 0.000 claims abstract description 22
- 229920005989 resin Polymers 0.000 claims abstract description 22
- 229930182556 Polyacetal Natural products 0.000 claims abstract description 18
- 229920006324 polyoxymethylene Polymers 0.000 claims abstract description 18
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 17
- 239000000194 fatty acid Substances 0.000 claims description 17
- 229930195729 fatty acid Natural products 0.000 claims description 17
- 229920001903 high density polyethylene Polymers 0.000 claims description 15
- 239000004700 high-density polyethylene Substances 0.000 claims description 15
- -1 silane compound Chemical class 0.000 claims description 14
- 229920001296 polysiloxane Polymers 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 239000013078 crystal Substances 0.000 claims description 9
- 239000003607 modifier Substances 0.000 claims description 9
- 239000002245 particle Substances 0.000 claims description 9
- 150000004665 fatty acids Chemical class 0.000 claims description 7
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 229910000077 silane Inorganic materials 0.000 claims description 4
- 150000005846 sugar alcohols Polymers 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 3
- 125000003700 epoxy group Chemical group 0.000 claims description 3
- 150000004671 saturated fatty acids Chemical class 0.000 claims description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical group CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 125000000524 functional group Chemical group 0.000 claims description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 229910052623 talc Inorganic materials 0.000 abstract description 10
- 239000000454 talc Substances 0.000 abstract description 9
- 238000005299 abrasion Methods 0.000 abstract description 8
- 239000003365 glass fiber Substances 0.000 abstract description 8
- 230000002195 synergetic effect Effects 0.000 abstract description 4
- 239000000945 filler Substances 0.000 abstract description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract description 2
- 229910052725 zinc Inorganic materials 0.000 abstract description 2
- 239000011701 zinc Substances 0.000 abstract description 2
- 238000013329 compounding Methods 0.000 abstract 2
- 230000000052 comparative effect Effects 0.000 description 16
- 230000000694 effects Effects 0.000 description 8
- 238000000465 moulding Methods 0.000 description 8
- 230000003014 reinforcing effect Effects 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 238000004898 kneading Methods 0.000 description 6
- 239000000835 fiber Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 150000002148 esters Chemical group 0.000 description 4
- 239000011159 matrix material Substances 0.000 description 4
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 229920002545 silicone oil Polymers 0.000 description 3
- GWFGDXZQZYMSMJ-UHFFFAOYSA-N Octadecansaeure-heptadecylester Natural products CCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCC GWFGDXZQZYMSMJ-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 238000000635 electron micrograph Methods 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- NKBWPOSQERPBFI-UHFFFAOYSA-N octadecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCC NKBWPOSQERPBFI-UHFFFAOYSA-N 0.000 description 2
- 229920000620 organic polymer Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000012779 reinforcing material Substances 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 239000012756 surface treatment agent Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 1
- WZUNUACWCJJERC-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)butyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CC)(CO)CO WZUNUACWCJJERC-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- PBWGCNFJKNQDGV-UHFFFAOYSA-N 6-phenylimidazo[2,1-b][1,3]thiazol-5-amine Chemical compound N1=C2SC=CN2C(N)=C1C1=CC=CC=C1 PBWGCNFJKNQDGV-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 239000004129 EU approved improving agent Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- PYVHTIWHNXTVPF-UHFFFAOYSA-N F.F.F.F.C=C Chemical compound F.F.F.F.C=C PYVHTIWHNXTVPF-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920009382 Polyoxymethylene Homopolymer Polymers 0.000 description 1
- 229920005027 Ultraform® Polymers 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- OCKWAZCWKSMKNC-UHFFFAOYSA-N [3-octadecanoyloxy-2,2-bis(octadecanoyloxymethyl)propyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCCCC)(COC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC OCKWAZCWKSMKNC-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 229940090958 behenyl behenate Drugs 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 125000004773 chlorofluoromethyl group Chemical group [H]C(F)(Cl)* 0.000 description 1
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000006298 dechlorination reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 229920006351 engineering plastic Polymers 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 1
- 229940078812 myristyl myristate Drugs 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000005704 oxymethylene group Chemical group [H]C([H])([*:2])O[*:1] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical class [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000010689 synthetic lubricating oil Substances 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- DZKXJUASMGQEMA-UHFFFAOYSA-N tetradecyl tetradecanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC DZKXJUASMGQEMA-UHFFFAOYSA-N 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は精密機器や電子・電気機
器の部品等に用いられる摺動摩擦性能に優れた複合樹脂
組成物に関し、さらに詳しくは摩擦係数、摩耗量が小さ
く、寸法精度の優れた複合樹脂組成物に関するものであ
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a composite resin composition excellent in sliding friction performance used for parts of precision equipment and electronic / electrical equipment, and more specifically, it has a small coefficient of friction, a small amount of wear and excellent dimensional accuracy. And a composite resin composition.
【0002】[0002]
【従来の技術】ポリアセタール樹脂はその卓越した摺動
性を生かして精密機器や電子・電気機器の部品等、特に
摺動性を必要とされる箇所に用いられていた。2. Description of the Related Art Polyacetal resins have been used in precision equipment, parts of electronic / electrical equipment, etc., particularly in places where slidability is required, by taking advantage of their excellent slidability.
【0003】しかしながら、近年ポリアセタール樹脂の
用途拡大に伴い、摺動性のみならず、剛性、強度、寸法
精度をも要求される事例が増えつつあるのが現状であ
る。その際には、通常ガラス繊維、タルク等の無機物を
添加して用いている。However, in recent years, along with the expansion of applications of polyacetal resins, there are increasing cases in which not only slidability but also rigidity, strength, and dimensional accuracy are required. In that case, an inorganic substance such as glass fiber or talc is usually added and used.
【0004】[0004]
【発明が解決しようとする課題】しかしながら、これら
従来の複合樹脂組成物は、摩擦係数が高く、摩耗量が多
いため、摺動摩擦性能を要求される箇所には使用でき
ず、又ガラス繊維、タルク等は成形物中での配向が強
く、さらにポリアセタール樹脂の高い結晶化度とあいま
って寸法精度が悪いという課題があった。However, since these conventional composite resin compositions have a high coefficient of friction and a large amount of wear, they cannot be used in places where sliding friction performance is required, and glass fiber and talc cannot be used. Etc. had a problem that the orientation in the molded product was strong and the dimensional accuracy was poor in combination with the high crystallinity of the polyacetal resin.
【0005】本発明はこのような問題点に鑑み、摩擦係
数、摩耗量が小さく、剛性、強度、寸法精度の優れた複
合樹脂組成物を提供することを目的とする。In view of such problems, it is an object of the present invention to provide a composite resin composition having a small coefficient of friction, a small amount of wear, and excellent rigidity, strength and dimensional accuracy.
【0006】[0006]
【課題を解決するための手段】本発明者らが上記課題に
対して鋭意研究を重ねた結果、ポリアセタール樹脂に酸
化亜鉛ウィスカと特定の摩耗改良剤の併用添加が有効で
あり、さらに酸化亜鉛ウィスカと特定の摩耗改良剤の添
加量がある範囲に限定された時及び酸化亜鉛ウィスカの
表面処理剤をある特定の表面処理剤に限定したときに特
に有効であることを見出し、本発明を完成するに至っ
た。本発明の複合樹脂組成物は、以下の要件を具備する
ものである。Means for Solving the Problems As a result of intensive studies conducted by the present inventors on the above problems, it is effective to add a zinc oxide whisker and a specific wear improving agent together to a polyacetal resin. And that the addition amount of a specific wear-improving agent is limited to a certain range and when the surface treatment agent for zinc oxide whiskers is limited to a specific surface treatment agent, the present invention is completed, and the present invention is completed. Came to. The composite resin composition of the present invention has the following requirements.
【0007】即ち、ポリアセタール樹脂と、酸化亜鉛ウ
ィスカを主成分とし、さらに摩耗改良剤から成ることを
特徴とする複合樹脂組成物である。That is, a composite resin composition comprising a polyacetal resin, a zinc oxide whisker as a main component, and an abrasion improver.
【0008】好適には、酸化亜鉛ウィスカの添加量が5
〜40重量%、摩耗改良剤の添加量が0.5〜30重量
%であり、酸化亜鉛ウィスカは核部とこの核部から異な
る複数方向に伸びた針状結晶部とを有し、針状結晶部の
基部から先端までの長さが2μm以上であり、摩耗改良
剤が、フッ素樹脂、シリコーン、高密度ポリエチレン、
脂肪酸エステルの1種又は2種以上から選択される。Preferably, the amount of zinc oxide whiskers added is 5
˜40% by weight, the amount of the wear modifier added is 0.5 to 30% by weight, and the zinc oxide whiskers have a core portion and needle-shaped crystal portions extending in different directions from the core portion. The length from the base of the crystal part to the tip is 2 μm or more, and the wear improver is fluororesin, silicone, high density polyethylene,
It is selected from one or more fatty acid esters.
【0009】[0009]
【作用】本発明で用いるポリアセタール樹脂は、メタノ
ールの酸化によるホルムアルデヒドまたはホルムアルデ
ヒドの三量体であるトリオキサンを主原料とするもので
あり、ポリオキシメチレンホモポリマー又は主鎖の大部
分がオキシメチレン連鎖よりなるポリアセタールコポリ
マー、ターポリマー等を含み、商業的に入手可能なもの
である。又、重合度についても特に制限はない。The polyacetal resin used in the present invention has a main raw material of trioxane which is formaldehyde or a trimer of formaldehyde obtained by oxidation of methanol. Most of the polyoxymethylene homopolymer or the main chain of the polyacetal resin is more than oxymethylene chain. And polyacetal copolymers, terpolymers, etc., which are commercially available. Also, the degree of polymerization is not particularly limited.
【0010】本発明の最大の特徴は、核部とこの核部か
ら異なる複数方向に伸びた針状結晶部とを有するテトラ
ポット状構造を有する酸化亜鉛ウィスカを用いることで
あり、その形状から容易に想像できるようにマトリック
ス樹脂中の物性値の3次元的等方性を保障し、成形物の
射出方向及び射出方向に対して直角方向の収縮率の差を
最小限に止め、高い寸法精度を確保し、フィラーとして
の本来の補強性を同時に得ることができる。The greatest feature of the present invention is to use a zinc oxide whisker having a tetrapot-like structure having a core portion and needle-like crystal portions extending from the core portion in different directions. As you can imagine, the three-dimensional isotropy of the physical properties in the matrix resin is guaranteed, and the difference in the shrinkage rate between the injection direction of the molded product and the direction perpendicular to the injection direction is minimized to achieve high dimensional accuracy. It is possible to secure and simultaneously obtain the original reinforcing property as a filler.
【0011】酸化亜鉛ウィスカの添加量は5〜40重量
%、より好ましくは5〜30重量%である。この範囲よ
り添加量が多いと混練が困難になるのみならず、摩耗特
性に対しても悪影響を及ぼして好ましくなく、この範囲
より添加量が少ないと酸化亜鉛ウィスカ添加の効果が発
揮されない。The amount of zinc oxide whiskers added is 5 to 40% by weight, more preferably 5 to 30% by weight. If the amount added is more than this range, not only the kneading becomes difficult, but also the wear characteristics are adversely affected, which is not preferable, and if the amount added is less than this range, the effect of adding zinc oxide whiskers is not exhibited.
【0012】又、酸化亜鉛ウィスカは平均繊維長約20
〜30μmの微細繊維であるため、成形物の表面平滑性
を確保し、摩擦係数の低下を最小限に止めながら、補強
効果を得ることができ、さらに上記理由より成形物中で
の等方的均一分散が容易に実現するため、耐摩耗特性の
低下を最小限に止めることができる点が他の繊維状、粒
子状、板状無機物との最大の相違点である。Zinc oxide whiskers have an average fiber length of about 20.
Since it is a fine fiber of ˜30 μm, it is possible to secure the surface smoothness of the molded product and to obtain the reinforcing effect while minimizing the reduction of the friction coefficient. The greatest difference from other fibrous, particulate, and plate-like inorganic substances is that the uniform dispersion can be easily realized and the deterioration of the abrasion resistance can be minimized.
【0013】図1は本発明で用いる酸化亜鉛ウィスカの
外観図であり、その形状特異性が容易に確認できる。FIG. 1 is an external view of a zinc oxide whisker used in the present invention, and its shape specificity can be easily confirmed.
【0014】また、この酸化亜鉛ウィスカは、金属亜鉛
粒子を加熱処理して得られ、それ自体きわめて量産的で
あり、バンバリーミキサー、スクリュー押出機、ロール
ミル等通常の樹脂混練法により容易に分散され、特別な
構成や工法を追加する必要はない。The zinc oxide whiskers are obtained by heat-treating metallic zinc particles and are extremely mass-producible by themselves. They are easily dispersed by a usual resin kneading method such as a Banbury mixer, a screw extruder, a roll mill, There is no need to add any special structure or construction method.
【0015】又、酸化亜鉛ウィスカは、マトリックス樹
脂との結合力を向上し、又ポリアセタール樹脂の劣化を
最小限に止めるため、予めシラン系化合物及び/又は脂
肪酸で表面処理することが望ましい。Further, the zinc oxide whiskers are preferably surface-treated in advance with a silane compound and / or a fatty acid in order to improve the binding force with the matrix resin and to minimize the deterioration of the polyacetal resin.
【0016】このシラン系化合物は、一般式 Y−R−Si−X3 で表現されるものであり、Yはアミノ基、エポキシ基、
ビニル基等の有機官能基であり、好ましくはエポキシ基
である。又、Rはアルキレン基等、Xは塩素、アルコキ
シ基、アセトン基等の加水分解性の基である。[0016] The silane compound are those represented by the general formula Y-R-Si-X 3 , Y is an amino group, an epoxy group,
It is an organic functional group such as a vinyl group, preferably an epoxy group. Further, R is an alkylene group or the like, and X is a hydrolyzable group such as chlorine, an alkoxy group or an acetone group.
【0017】又、脂肪酸は炭素数12〜28であること
が必須であり、これらに属するものとしてはステアリン
酸、ラウリン酸、ミリスチン酸、パルミチン酸、オレイ
ン酸、リノール酸、リノレン酸、及びこれら脂肪酸の金
属塩が含まれ、この内特に炭素数12〜28の飽和脂肪
酸が好ましい。It is essential that the fatty acid has 12 to 28 carbon atoms, and those belonging to these include stearic acid, lauric acid, myristic acid, palmitic acid, oleic acid, linoleic acid, linolenic acid, and these fatty acids. The metal salt of is included, and among them, saturated fatty acids having 12 to 28 carbon atoms are particularly preferable.
【0018】さらに、酸化亜鉛ウィスカは、針状結晶部
の基部から先端までの長さが2μm以上であることが望
ましい。これは2μm以下の酸化亜鉛ウィスカはマトリ
ックス樹脂中で単なる球状粒子としてしか作用せず、補
強効果が得られないからである。Further, the zinc oxide whiskers preferably have a length from the base to the tip of the needle-shaped crystal portion of 2 μm or more. This is because zinc oxide whiskers having a diameter of 2 μm or less act only as spherical particles in the matrix resin, and the reinforcing effect cannot be obtained.
【0019】又、マトリックス樹脂中に針状の酸化亜鉛
ウィスカが存在することがあるが、これは複数方向に伸
びた針状結晶部が折損したものであり、針状繊維として
作用し、折損した後も成形物中で等方的に均一分散して
いることが実験的に確認されており、本発明の主要特性
を損なうものではない。Needle-shaped zinc oxide whiskers may be present in the matrix resin, but these are broken pieces of needle-shaped crystal parts extending in a plurality of directions, acting as needle-shaped fibers and broken. It has been experimentally confirmed that it is isotropically uniformly dispersed in the molded product after that, and it does not impair the main characteristics of the present invention.
【0020】摩耗改良剤は、成形物中に存在する酸化亜
鉛ウィスカと相乗的に機能し、摩擦係数、摩耗量の低下
に寄与するものであり、フッ素樹脂、シリコーン、高密
度ポリエチレン、二硫化モリブデン、脂肪酸エステル、
低分子量ポリエチレンワックス、金属石鹸、脂肪アルコ
ール、多価アルコール、鉱油、植物油、合成潤滑油等が
挙げられる。この中で、特にフッ素樹脂、シリコーン、
高密度ポリエチレン、脂肪酸エステルの1種又は2種以
上の添加が好ましい。The wear modifier functions synergistically with the zinc oxide whiskers present in the molded product, and contributes to the reduction of the friction coefficient and wear amount. Fluororesin, silicone, high density polyethylene, molybdenum disulfide. , Fatty acid ester,
Examples thereof include low molecular weight polyethylene wax, metal soap, fatty alcohol, polyhydric alcohol, mineral oil, vegetable oil and synthetic lubricating oil. Among them, especially fluororesin, silicone,
It is preferable to add one or more of high-density polyethylene and fatty acid ester.
【0021】摩耗改良剤の添加量は、0.5〜30重量
%であり、好ましくは1〜20重量%である。添加量が
これより少ないと摩耗改良効果が得られず、添加量がこ
れより多いと、例えばシリコーン、脂肪酸エステルの場
合成形物表面へ滲み出し、べとつく現象を発生させ、又
成形時にスクリューへの食い込み不良を起こし、著しい
場合は成形困難となり好ましくない。又、高密度ポリエ
チレン、フッ素樹脂の場合分散性が悪化し、摩耗改良効
果が低下するのみならず、混練が困難となり好ましくな
い。The amount of the wear modifier added is 0.5 to 30% by weight, preferably 1 to 20% by weight. If the added amount is less than this, the wear improving effect cannot be obtained, and if the added amount is more than this, for example, in the case of silicone or fatty acid ester, it exudes to the surface of the molded product and causes a sticky phenomenon, and it also bites into the screw during molding. If it causes a defect and is remarkable, molding becomes difficult, which is not preferable. Further, in the case of high density polyethylene or fluororesin, the dispersibility is deteriorated, the effect of improving wear is lowered, and kneading is difficult, which is not preferable.
【0022】ここでのフッ素樹脂とは、CHClF2 の
熱分解で得られるテトラフルオロエチレンの重合体であ
る四フッ化エチレン、テトラフルオロエチレンとヘキサ
フルオロプロピレンを共重合して得られるテトラフルオ
ロエチレン−ヘキサフルオロプロピレン共重合体、CF
2 Cl−CFCl2 の脱塩素によって得られるクロロト
リフルオロエチレンの共重合体である三フッ化エチレ
ン、フッ化ビニリデンのラジカル重合体であるポリフッ
化ビニリデン等があり、摩耗改良剤としては摩擦係数、
表面エネルギーが小さい四フッ化エチレンが好ましい。
又、フッ素樹脂の平均粒径は30μm以下であることが
好ましい。平均粒径が30μmを越えると成形物中での
均一分散が困難となり、四フッ化エチレンの摩耗改良効
果が充分に発揮されなくなる。The fluororesin here means tetrafluoroethylene, which is a polymer of tetrafluoroethylene obtained by thermal decomposition of CHClF 2 , or tetrafluoroethylene-obtained by copolymerizing tetrafluoroethylene and hexafluoropropylene. Hexafluoropropylene copolymer, CF
2 Cl-CFCl 2 of ethylene trifluoride copolymers of the resulting chlorotrifluoroethylene by dechlorination, there is polyvinylidene fluoride or the like as a radical polymerization of vinylidene fluoride, the coefficient of friction as a wear improving agents,
Ethylene tetrafluoride having a low surface energy is preferable.
The average particle size of the fluororesin is preferably 30 μm or less. If the average particle size exceeds 30 μm, it becomes difficult to uniformly disperse the particles in the molded product, and the effect of improving wear of tetrafluoroethylene cannot be sufficiently exhibited.
【0023】シリコーンは、一般的にオルガノポリシロ
キサンと称されるシリコーン油、シリコーンゴム、シリ
コーン樹脂等である。特に流動性を損なわない比較的重
合度の低いジメチルポリシロキサン等からなるシリコー
ン油、シリコーン油に金属石鹸等を添加したシリコーン
グリスが好ましい。The silicone is silicone oil, silicone rubber, silicone resin or the like which is generally called organopolysiloxane. In particular, silicone oil made of dimethylpolysiloxane or the like having a relatively low degree of polymerization that does not impair fluidity, and silicone grease obtained by adding metal soap or the like to silicone oil are preferable.
【0024】高密度ポリエチレンは、エチレンを重合し
て得られる密度0.94g/cm3 程度以上のものであ
り、炭素数6以上の長鎖分岐が大部分をしめる結晶構造
を有し、エチレンと共重合し得るα−オレフィン等との
共重合物も含まれる。高密度ポリエチレンの平均粒径は
200μm以下であり、分子量は50000〜8000
000であり、より好ましくは分子量が2000000
以上の所謂超高密度ポリエチレンと称されるものが好ま
しい。平均粒径が200μmを越えると成形物の表面が
粗くなり、摩擦係数が上昇し好ましくない。又、分子量
が50000より少ないと、混練により成形物中で高密
度ポリエチレンが粒子状で存在することが困難となり、
摩耗特性改良に寄与しなくなり好ましくない。又、分子
量が8000000を越えると混練が著しく困難とな
り、著しい場合は成形困難となり好ましくない。The high-density polyethylene has a density of about 0.94 g / cm 3 or more obtained by polymerizing ethylene, has a crystal structure in which long-chain branches having 6 or more carbon atoms mostly occupy, and Also included are copolymers with copolymerizable α-olefins and the like. The high-density polyethylene has an average particle size of 200 μm or less and a molecular weight of 50,000 to 8,000.
And more preferably a molecular weight of 2,000,000.
The above-mentioned so-called ultra-high density polyethylene is preferable. If the average particle size exceeds 200 μm, the surface of the molded product becomes rough and the coefficient of friction increases, which is not preferable. If the molecular weight is less than 50,000, it becomes difficult for the high density polyethylene to exist in the form of particles in the molded product due to kneading.
It is not preferable because it does not contribute to the improvement of wear characteristics. Further, if the molecular weight exceeds 8,000,000, kneading becomes extremely difficult, and if it is remarkable, molding becomes difficult, which is not preferable.
【0025】脂肪酸エステルは、炭素数5〜23の脂肪
酸と炭素数2〜30の一価又は多価アルコールとのエス
テルであり、より好ましくは炭素数12〜22の脂肪酸
と炭素数2〜22の一価又は多価アルコールとのエステ
ルである。これらに属するエステルの例としては、ステ
アリルステアレート、ペンタエリスリトールモノステア
レート、ペンタエリスリトールテトラステアレート、ベ
ヘニルベヘネート、ミリスチルミリステート等が挙げら
れる。The fatty acid ester is an ester of a fatty acid having 5 to 23 carbon atoms and a monohydric or polyhydric alcohol having 2 to 30 carbon atoms, and more preferably a fatty acid having 12 to 22 carbon atoms and 2 to 22 carbon atoms. Esters with monohydric or polyhydric alcohols. Examples of the esters belonging to these include stearyl stearate, pentaerythritol monostearate, pentaerythritol tetrastearate, behenyl behenate, myristyl myristate, and the like.
【0026】[0026]
【実施例】以下、本発明のいくつかの実施例について説
明するが、本発明はこれら実施例に限定されるものでは
ない。EXAMPLES Some examples of the present invention will be described below, but the present invention is not limited to these examples.
【0027】各実施例に用いた試料、試験装置、試験方
法は以下の通りである。The samples, test equipment, and test methods used in each example are as follows.
【0028】(試料) *ポリアセタール樹脂 BASFエンジニアリングプラスチック(株)製 ウルトラフォルムW2320 *酸化亜鉛ウィスカ 松下アムテック(株)製、パナテトラ(登録商標)(表
面処理品) *フッ素樹脂 三井デュポンフロロケミカル(株)製、MP1300 *シリコーン 信越シリコン(株)製、KF−96 *高密度ポリエチレン 三井石油化学工業(株)製、ミペロン(登録商標)XM
−220 *脂肪酸エステル ステアリルステアレート *ガラス繊維 日本板硝子(株)製、RESO3−TP87 *タルク 富士タルク(株)製、PKP−80 (試験方法) *曲げ強度 :ASTM−D790 *曲げ弾性率 :ASTM−D790 *引張破断強度:ASTM−D638 *摩擦摩耗試験:鈴木式摩耗試験機を使用。相手材S4
5C(無潤滑)。(Sample) * Polyacetal resin manufactured by BASF Engineering Plastics Co., Ltd. Ultraform W2320 * Zinc oxide whisker manufactured by Matsushita Amtec Co., Ltd., Panatetra (registered trademark) (surface treated product) * Fluorine resin Mitsui DuPont Fluorochemicals Co., Ltd. Made, MP1300 * Silicone, Shin-Etsu Silicon Co., Ltd., KF-96 * High-density polyethylene Mitsui Petrochemical Co., Ltd., Miperon (registered trademark) XM
-220 * Fatty acid ester stearyl stearate * Glass fiber Nippon Sheet Glass Co., Ltd., RESO3-TP87 * Talc Fuji Talc Co., Ltd. PKP-80 (Test method) * Bending strength: ASTM-D790 * Bending elastic modulus: ASTM -D790 * Tensile breaking strength: ASTM-D638 * Friction and wear test: Using Suzuki type wear tester. Counterpart material S4
5C (no lubrication).
【0029】摩擦速度30cm/sec、加重10kg/cm2、摩
擦距離10km時点で摩擦係数、比摩擦量を測定。The friction coefficient and the specific friction amount were measured at a friction speed of 30 cm / sec, a load of 10 kg / cm 2 , and a friction distance of 10 km.
【0030】*成形収縮率 :ASTM−D955準拠
型使用。* Molding shrinkage ratio: A mold conforming to ASTM-D955 is used.
【0031】厚さ1mm、直径102mm、ゲート幅12.
7mm、金型温度80°C *試料作成 :スクリュー押出機(温度180°C、
スクリュー径44mm、2軸) 射出成形機(温度190°C、圧力850kg/cm2、トー
タルサイクル60sec ) 各実施例及び比較例の結果を表1〜表4にまとめて示
す。Thickness 1 mm, diameter 102 mm, gate width 12.
7 mm, mold temperature 80 ° C * Sample preparation: Screw extruder (temperature 180 ° C,
Screw diameter 44 mm, biaxial) Injection molding machine (temperature 190 ° C, pressure 850 kg / cm 2 , total cycle 60 sec) The results of each Example and Comparative Example are summarized in Tables 1 to 4.
【0032】[0032]
【表1】 [Table 1]
【0033】[0033]
【表2】 [Table 2]
【0034】[0034]
【表3】 [Table 3]
【0035】[0035]
【表4】 [Table 4]
【0036】(実施例1〜3及び比較例1〜3、9)実
施例1〜3はそれぞれポリアセタール樹脂に対し、エポ
キシシラン系表面処理を施された酸化亜鉛ウィスカを
5、10、30重量%添加した例であり、添加量につれ
て優れた補強効果が認められ、成形収縮率の異方性も殆
ど認められないことが分かる。又、比較例1に示すポリ
アセタールのみと比べても、動摩擦係数は殆ど変化せ
ず、比摩耗量の増加も最小限に抑えられており、このま
までも摺動性、強度、剛性、寸法精度の点で優れた複合
樹脂組成物である。(Examples 1 to 3 and Comparative Examples 1 to 3 and 9) In Examples 1 to 3, 5, 10 and 30% by weight of zinc oxide whiskers surface-treated with epoxysilane were added to the polyacetal resin. It is an example of addition, and it can be seen that an excellent reinforcing effect is recognized with the addition amount and almost no anisotropy of molding shrinkage is recognized. Further, compared with only the polyacetal shown in Comparative Example 1, the dynamic friction coefficient hardly changed, and the increase of the specific wear amount was suppressed to the minimum, and the sliding property, strength, rigidity, and dimensional accuracy were kept as they were. Which is an excellent composite resin composition.
【0037】比較例2、3はポリアセタール樹脂に対
し、ガラス繊維、タルクを20重量%添加した例であ
り、従来より極めて多く用いられていた例である。特徴
的なことは、これらガラス繊維、タルクを用いると単な
る剛性、強度は得られるものの、比較例にもあるように
摺動性が著しく悪化し、特に比摩耗量の増加が著しいこ
と、さらにガラス繊維、タルクの配向が大きいため成形
収縮率の異方性が大きくなり、高い寸法精度が得られな
いこと、以上2点が実施例1〜3に示した組成物との最
大の相違点であり、本発明の着目点である。Comparative Examples 2 and 3 are examples in which glass fibers and talc were added to the polyacetal resin in an amount of 20% by weight, which are examples that have been used much more than before. Characteristically, when using these glass fibers and talc, although simple rigidity and strength can be obtained, slidability is remarkably deteriorated as in the comparative example, and in particular, the specific wear amount is remarkably increased. Since the orientation of the fibers and talc is large, the anisotropy of the molding shrinkage becomes large, and high dimensional accuracy cannot be obtained. The above two points are the biggest differences from the compositions shown in Examples 1 to 3. That is the point of interest of the present invention.
【0038】又、比較例9は実施例3と同じ配合で酸化
亜鉛ウィスカに表面処理をしていない例であり、力学的
物性、摺動性とも実施例3と比べて悪化しており、本発
明の目的から考えて好ましくない。又、混練時にポリア
セタールの分解が発生し、ストランド引きが著しく困難
であった。Further, Comparative Example 9 is an example in which the zinc oxide whiskers were not surface-treated with the same composition as in Example 3, and the mechanical properties and slidability were worse than in Example 3, and It is not preferable for the purpose of the invention. Further, the polyacetal was decomposed during the kneading, and it was extremely difficult to draw the strand.
【0039】(実施例4)実施例3と同じ配合で酸化亜
鉛ウィスカの表面処理剤をステアリン酸としたものであ
る。この場合は実施例3と比べて僅かながら力学物性が
低下しているものの本発明の主目的である摺動性、成形
収縮率の異方性緩和、補強効果は満足の行く値が得られ
ていることが分かる。(Example 4) A zinc oxide whisker surface treating agent was stearic acid with the same composition as in Example 3. In this case, although the mechanical properties were slightly lowered as compared with Example 3, satisfactory values were obtained for the slidability, the anisotropy relaxation of the molding shrinkage, and the reinforcing effect, which are the main objects of the present invention. I understand that
【0040】(実施例5〜8及び比較例4、10)実施
例5〜8は、エポキシシラン系表面処理の施された酸化
亜鉛ウィスカを10、20重量%、フッ素樹脂を5、1
0重量%添加した例であり、フッ素の添加により実施例
1〜3と比べてさらに摺動性が改善されていることが分
かる。さらに特徴的なことは、実施例6、8で示す比摩
耗量が比較例10に示すフッ素樹脂のみの添加と比べて
少ない点であり、これは酸化亜鉛ウィスカとフッ素樹脂
とが相乗的に作用し実現したものである。又、実施例1
〜3でみられた補強効果、成形収縮率の異方性緩和効果
は維持されていることが分かる。(Examples 5 to 8 and Comparative Examples 4 and 10) In Examples 5 to 8, 10, 20% by weight of zinc oxide whiskers subjected to epoxysilane surface treatment and 5, 1 of fluororesin were used.
This is an example in which 0% by weight is added, and it can be seen that the addition of fluorine further improves the slidability as compared with Examples 1 to 3. What is more characteristic is that the specific wear amounts shown in Examples 6 and 8 are smaller than the addition of the fluororesin alone shown in Comparative Example 10, which means that the zinc oxide whiskers and the fluororesin act synergistically. It was realized. In addition, Example 1
It can be seen that the reinforcing effect and the effect of alleviating the anisotropy of molding shrinkage, which are observed in Nos. 3 to 3, are maintained.
【0041】又、比較例4は比較例2にフッ素樹脂を1
0重量%添加した例であり、フッ素の効果により摺動性
は改善されたが、不十分であり、実施例5〜8に見られ
た相乗効果は確認されないことが分かる。In Comparative Example 4, the fluororesin was added to Comparative Example 2
It is an example in which 0 wt% was added, and although the slidability was improved by the effect of fluorine, it was found to be insufficient, and the synergistic effect seen in Examples 5 to 8 was not confirmed.
【0042】(実施例9〜13及び比較例5〜8、11
〜13)実施例9〜14はエポキシシラン系表面処理の
施された酸化亜鉛ウィスカを10重量%、シリコーン、
高密度ポリエチレン、脂肪酸エステルを3〜10重量%
の範囲で添加したものである。実施例5〜8で見られた
のと同様に、実施例9と比較例11、実施例12と比較
例12、実施例13と比較例13においても、酸化亜鉛
ウィスカと各種摩耗改良剤が相乗的に作用していること
が容易に理解できる。(Examples 9 to 13 and Comparative Examples 5 to 8 and 11)
Examples 13 to 14 are 10% by weight of zinc oxide whiskers surface-treated with epoxysilane, silicone,
High-density polyethylene, 3-10 wt% of fatty acid ester
Is added in the range of. Similar to what was seen in Examples 5 to 8, also in Example 9 and Comparative Example 11, Example 12 and Comparative Example 12, and Example 13 and Comparative Example 13, zinc oxide whiskers and various wear modifiers were synergistic. It is easy to understand that they are working.
【0043】又、比較例5〜8はガラス繊維、タルクに
シリコーン、高密度ポリエチレン、脂肪酸エステルを併
用添加した例であり、比較例4と同様これら摩耗改良剤
の添加により摺動性の改善効果が見られるが不十分であ
り、シリコーン、高密度ポリエチレン、脂肪酸エステル
の添加は摺動性改善効果は全く見出されていないことが
分かる。Comparative Examples 5 to 8 are examples in which glass fiber, talc, and silicone, high-density polyethylene, and fatty acid ester are added together. Similar to Comparative Example 4, the addition of these wear modifiers improves the slidability. However, the addition of silicone, high-density polyethylene, and fatty acid ester has not been found to have any slidability improving effect.
【0044】(実施例14)エポキシシラン系表面処理
の施された酸化亜鉛ウィスカ20重量%にフッ素樹脂、
高密度ポリエチレンを各10重量%添加した例であり、
摩耗改良剤を複数種添加した場合においても実施例1〜
13で見られた基本効果は見出すことができ、より一層
摺動性改善が実現されていることが分かる。Example 14 20% by weight of zinc oxide whiskers surface-treated with an epoxysilane-based fluororesin,
It is an example in which each high-density polyethylene is added by 10% by weight,
Even when a plurality of types of wear modifiers are added, Examples 1 to 1
The basic effect seen in No. 13 can be found, and it can be seen that the slidability is further improved.
【0045】なお、上記本実施例では特に加えなかった
一般的な各種の酸化防止剤、紫外線吸収剤等の安定剤、
難燃剤、核剤及び一般的な顔料、染料等の添加は任意に
なし得ることは言うまでもなく、又本発明特性を損なわ
ない範囲において従来公知の各種有機高分子の1種又は
2種以上の添加も可能である。これらに該当する有機高
分子の例としては、ポリウレタン、エチレン酢酸ビニル
共重合体、エチレン−アルキルアクリレート共重合体、
スチレン−ブタジエン−アクリロニトリル共重合体、ポ
リアクリレートからなる多相グラフトル共重合体、熱可
塑性エラストマー等が挙げられる。Various general antioxidants, stabilizers such as ultraviolet absorbers, which are not particularly added in the above-mentioned embodiment,
It goes without saying that flame retardants, nucleating agents and general pigments, dyes, etc. can be added arbitrarily, and one or more kinds of conventionally known various organic polymers are added within a range not impairing the characteristics of the present invention. Is also possible. Examples of organic polymers corresponding to these are polyurethane, ethylene vinyl acetate copolymer, ethylene-alkyl acrylate copolymer,
Examples thereof include a styrene-butadiene-acrylonitrile copolymer, a polyacrylate multi-phase graft copolymer, and a thermoplastic elastomer.
【0046】又、本発明では特に加えなったが、剛性、
強度をさらに高める目的で従来より公知の一般的な補強
物質の添加は、本発明の目的を損なわない範囲で任意に
なし得ることは、本発明の主眼である摩耗特性及び寸法
精度の改質が、酸化亜鉛ウィスカの形状特異性及び酸化
亜鉛ウィスカと摩耗改良剤との相乗効果によって実現さ
れていることを考えれば容易に理解し得るものである。
これら無機物質に属するものとしてはガラスビーズ、炭
酸カルシウム、石英粉、シリカ、炭酸マグネシウム、硫
酸バリウム、クレー、アルミナ粉、ガラス粉、グラファ
イト等の粒状無機物質、ガラス繊維、炭素繊維、ワラス
トナイト、ドロマイト、アスベスト、シリコンカーバイ
トウィスカ、チタン酸カリウムウィスカ、ウィスカ状炭
酸カルシウム、金属繊維、アラミド繊維等の繊維状補強
材、マイカ、ガラスフレーク、タルク、金属箔等の板状
補強材が挙げられる。Further, although not particularly added in the present invention, the rigidity,
The addition of a conventionally known general reinforcing substance for the purpose of further increasing the strength can be arbitrarily performed within a range that does not impair the purpose of the present invention. It can be easily understood by considering the shape specificity of the zinc oxide whiskers and the synergistic effect of the zinc oxide whiskers and the wear modifier.
As those belonging to these inorganic substances, glass beads, calcium carbonate, quartz powder, silica, magnesium carbonate, barium sulfate, clay, alumina powder, glass powder, granular inorganic substances such as graphite, glass fiber, carbon fiber, wollastonite, Examples thereof include fibrous reinforcing materials such as dolomite, asbestos, silicon carbide whiskers, potassium titanate whiskers, whisker-like calcium carbonate, metal fibers and aramid fibers, and plate-like reinforcing materials such as mica, glass flakes, talc and metal foil.
【0047】[0047]
【発明の効果】以上のように、本発明の複合樹脂組成物
は、摩擦係数、摩耗量が小さく、強度、剛性とともに寸
法精度に優れており、各種精密機器や電子・電気機器の
部品等で、特に摺動摩擦性能を要求される箇所に効果的
に用いることができる。。INDUSTRIAL APPLICABILITY As described above, the composite resin composition of the present invention has a small coefficient of friction, a small amount of wear, and excellent dimensional accuracy in addition to strength and rigidity, and is suitable for various precision instruments and electronic / electrical equipment parts. In particular, it can be effectively used in places where sliding friction performance is required. .
【図1】本発明に用いる酸化亜鉛ウィスカの電子顕微鏡
写真である。FIG. 1 is an electron micrograph of a zinc oxide whisker used in the present invention.
【手続補正書】[Procedure amendment]
【提出日】平成5年4月21日[Submission date] April 21, 1993
【手続補正1】[Procedure Amendment 1]
【補正対象書類名】明細書[Document name to be amended] Statement
【補正対象項目名】図1[Name of item to be corrected] Figure 1
【補正方法】変更[Correction method] Change
【補正内容】[Correction content]
【図1】酸化亜鉛ウィスカの結晶構造を示す電子顕微鏡
写真である。FIG. 1 is an electron micrograph showing a crystal structure of zinc oxide whiskers.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 C08L 23:06 83:04) (72)発明者 納村 和美 大阪府門真市大字門真1006番地 松下電器 産業株式会社内 (72)発明者 松尾 光二郎 大阪府門真市大字門真1006番地 松下電器 産業株式会社内─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification number Reference number in the agency FI technical display location C08L 23:06 83:04) (72) Inventor Kazumi Nanomura 1006 Kadoma, Kadoma, Osaka Prefecture Matsushita Electric Appliance Industry Co., Ltd. (72) Inventor Kojiro Matsuo 1006 Kadoma, Kadoma City, Osaka Prefecture Matsushita Electric Industrial Co., Ltd.
Claims (11)
カを主成分とする複合樹脂組成物。1. A composite resin composition containing a polyacetal resin and zinc oxide whiskers as main components.
されていることを特徴とする請求項1記載の複合樹脂組
成物。2. The composite resin composition according to claim 1, wherein a wear modifier is added to the polyacetal resin.
量%、摩耗改良剤の添加量が0.5〜30重量%である
ことを特徴とする請求項2記載の複合樹脂組成物。3. The composite resin composition according to claim 2, wherein the zinc oxide whiskers are added in an amount of 5 to 40% by weight and the wear modifier is added in an amount of 0.5 to 30% by weight.
ら異なる4軸方向に伸びた針状結晶部とを有し、針状結
晶部の基部から先端までの長さが2μm以上であること
を特徴とする請求項1又は2記載の複合樹脂組成物。4. A zinc oxide whisker has a core portion and needle-shaped crystal portions extending from the core portion in different four-axis directions, and the length from the base to the tip of the needle-shaped crystal portion is 2 μm or more. The composite resin composition according to claim 1 or 2, wherein
び/又は飽和脂肪酸で表面処理を施したものであること
を特徴とする請求項1又は2記載の複合樹脂組成物。5. The composite resin composition according to claim 1, wherein the zinc oxide whiskers are surface-treated with a silane compound and / or a saturated fatty acid.
性の基 における官能基Yがエポキシ基であることを特徴とする
請求項5記載の複合樹脂組成物。6. The functional group Y in the general formula of a silane-based compound Y—R—Si—X 3 R: an alkylene group or the like X 3 : a hydrolyzable group such as chlorine, an alkoxy group, or an acetone group is an epoxy group. The composite resin composition according to claim 5, wherein
ことを特徴とする請求項5記載の複合樹脂組成物。7. The composite resin composition according to claim 5, wherein the saturated fatty acid has 12 to 28 carbon atoms.
ン、高密度ポリエチレン、脂肪酸エステルの1種又は2
種以上から選択されていることを特徴とする請求項2記
載の複合樹脂組成物。8. The wear improving agent is one or two of fluororesin, silicone, high density polyethylene and fatty acid ester.
The composite resin composition according to claim 2, wherein the composite resin composition is selected from at least one species.
四フッ化エチレンであることを特徴とする請求項8記載
の複合樹脂組成物。9. The composite resin composition according to claim 8, wherein the fluororesin is tetrafluoroethylene having an average particle size of 30 μm or less.
0μm以下であり、分子量が50000〜800000
0であることを特徴とする請求項8記載の複合樹脂組成
物。10. The high-density polyethylene has an average particle size of 20.
0 μm or less and molecular weight of 50,000 to 800,000
It is 0, The composite resin composition of Claim 8 characterized by the above-mentioned.
原子を有する脂肪酸と、2〜30個の炭素原子を有する
一価又は多価アルコールから得たものであることを特徴
とする請求項8記載の複合樹脂組成物。11. The fatty acid ester is obtained from a fatty acid having 5 to 32 carbon atoms and a monohydric or polyhydric alcohol having 2 to 30 carbon atoms. The composite resin composition described.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7313891A JPH05255571A (en) | 1991-04-05 | 1991-04-05 | Composite resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7313891A JPH05255571A (en) | 1991-04-05 | 1991-04-05 | Composite resin composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH05255571A true JPH05255571A (en) | 1993-10-05 |
Family
ID=13509546
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7313891A Pending JPH05255571A (en) | 1991-04-05 | 1991-04-05 | Composite resin composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH05255571A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0791632A3 (en) * | 1996-02-23 | 1999-09-08 | Ticona GmbH | Resinous moulding matter having reduced wear |
JP2008520816A (en) * | 2004-11-23 | 2008-06-19 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | High density polyoxymethylene composition |
US8110056B2 (en) | 2003-08-06 | 2012-02-07 | Sumitomo Rubber Industries, Ltd. | Process for preparing studless tire with tread having zinc oxide whiskers, glass fibers and porous natural glass |
WO2014046006A1 (en) * | 2012-09-19 | 2014-03-27 | 第一精工株式会社 | Resin composition for forming ramps and ramp for magnetic disk devices |
JP2021024891A (en) * | 2019-07-31 | 2021-02-22 | 旭化成株式会社 | Polyacetal resin composition and molding |
-
1991
- 1991-04-05 JP JP7313891A patent/JPH05255571A/en active Pending
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0791632A3 (en) * | 1996-02-23 | 1999-09-08 | Ticona GmbH | Resinous moulding matter having reduced wear |
US8110056B2 (en) | 2003-08-06 | 2012-02-07 | Sumitomo Rubber Industries, Ltd. | Process for preparing studless tire with tread having zinc oxide whiskers, glass fibers and porous natural glass |
JP2008520816A (en) * | 2004-11-23 | 2008-06-19 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | High density polyoxymethylene composition |
WO2014046006A1 (en) * | 2012-09-19 | 2014-03-27 | 第一精工株式会社 | Resin composition for forming ramps and ramp for magnetic disk devices |
CN104640927A (en) * | 2012-09-19 | 2015-05-20 | 第一精工株式会社 | Resin composition for forming ramp and ramp for magnetic disk device |
JP2015163683A (en) * | 2012-09-19 | 2015-09-10 | 第一精工株式会社 | Ramp forming resin composition and magnetic disk drive lamp |
JP2021024891A (en) * | 2019-07-31 | 2021-02-22 | 旭化成株式会社 | Polyacetal resin composition and molding |
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