JPH0420093B2 - - Google Patents
Info
- Publication number
- JPH0420093B2 JPH0420093B2 JP59041934A JP4193484A JPH0420093B2 JP H0420093 B2 JPH0420093 B2 JP H0420093B2 JP 59041934 A JP59041934 A JP 59041934A JP 4193484 A JP4193484 A JP 4193484A JP H0420093 B2 JPH0420093 B2 JP H0420093B2
- Authority
- JP
- Japan
- Prior art keywords
- self
- locking
- composition
- nylon
- agent composition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 claims description 43
- 239000000463 material Substances 0.000 claims description 37
- 239000003822 epoxy resin Substances 0.000 claims description 20
- 229920000647 polyepoxide Polymers 0.000 claims description 20
- 239000002904 solvent Substances 0.000 claims description 16
- 238000007789 sealing Methods 0.000 claims description 7
- 239000004952 Polyamide Substances 0.000 claims description 5
- 229920002647 polyamide Polymers 0.000 claims description 5
- 239000000843 powder Substances 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000002245 particle Substances 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 description 36
- 239000004677 Nylon Substances 0.000 description 15
- 229920001778 nylon Polymers 0.000 description 15
- 238000011282 treatment Methods 0.000 description 14
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 10
- 239000012948 isocyanate Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 150000002513 isocyanates Chemical class 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 229920005992 thermoplastic resin Polymers 0.000 description 6
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 5
- 239000000853 adhesive Substances 0.000 description 5
- 230000001070 adhesive effect Effects 0.000 description 5
- -1 aniline aldehyde Chemical class 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 229920000571 Nylon 11 Polymers 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 229920001568 phenolic resin Polymers 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 229920003180 amino resin Polymers 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 150000003961 organosilicon compounds Chemical class 0.000 description 3
- 150000003377 silicon compounds Chemical class 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229920000299 Nylon 12 Polymers 0.000 description 2
- 229920002292 Nylon 6 Polymers 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000005238 degreasing Methods 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 239000005007 epoxy-phenolic resin Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 125000000466 oxiranyl group Chemical group 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical group CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- UMHKOAYRTRADAT-UHFFFAOYSA-N [hydroxy(octoxy)phosphoryl] octyl hydrogen phosphate Chemical compound CCCCCCCCOP(O)(=O)OP(O)(=O)OCCCCCCCC UMHKOAYRTRADAT-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000006482 condensation reaction Methods 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
- 239000007822 coupling agent Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- YWJUZWOHLHBWQY-UHFFFAOYSA-N decanedioic acid;hexane-1,6-diamine Chemical compound NCCCCCCN.OC(=O)CCCCCCCCC(O)=O YWJUZWOHLHBWQY-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- XHWQYYPUYFYELO-UHFFFAOYSA-N ditridecyl phosphite Chemical compound CCCCCCCCCCCCCOP([O-])OCCCCCCCCCCCCC XHWQYYPUYFYELO-UHFFFAOYSA-N 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000011221 initial treatment Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 238000005488 sandblasting Methods 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 238000009958 sewing Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- HQYALQRYBUJWDH-UHFFFAOYSA-N trimethoxy(propyl)silane Chemical compound CCC[Si](OC)(OC)OC HQYALQRYBUJWDH-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Landscapes
- Lubricants (AREA)
Description
【発明の詳細な説明】
この発明は、ねじ部材のゆるみ止め、位置調
整、或いはシーリング効果を具現するためのセル
フロツキング剤組成物及び、該組成物の性質を専
ら利用して製造したセルフロツキングねじ部材に
関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a self-locking agent composition for realizing the effects of locking, adjusting the position, or sealing a screw member, and a self-locking agent composition manufactured by exclusively utilizing the properties of the composition. This invention relates to a king screw member.
従来より、ボルト、ナツト等ねじ部材のゆるみ
止め対策としてねじ面に可塑性物質を添着するこ
とが広く行われている。この例として次の様な方
式が挙げられる。ねじ面に穿孔等の機械加工を
施し、熱可塑性樹脂を装着、埋込む方式。加熱
したねじ面に熱可塑性樹脂片を当接して圧着する
方式。熱可塑性樹脂粉末をねじ面に吹き付けそ
の後加熱融着する方式。ねじ面を予め化学的処
理、或いは、機械的処理(例えばサンドブラス
ト)して粗面化させ、熱可塑性樹脂粉末を融着さ
せる方式。ねじ面に予めプライマ処理等密着強
化処理を施し、熱可塑性樹脂を加熱融着させる方
式等である。 BACKGROUND ART Conventionally, as a measure to prevent screw members such as bolts and nuts from loosening, it has been widely practiced to attach a plastic substance to the screw surface. Examples of this method include the following methods. A method in which the screw surface is machined such as perforation, and thermoplastic resin is attached and embedded. A method in which a piece of thermoplastic resin is pressed against the heated screw surface. A method in which thermoplastic resin powder is sprayed onto the threaded surface and then heated and fused. A method in which the thread surface is roughened by chemical treatment or mechanical treatment (for example, sandblasting) in advance, and then thermoplastic resin powder is fused. This method involves applying adhesion strengthening treatment such as primer treatment to the threaded surface in advance, and then heat-sealing the thermoplastic resin.
ところが、上記従来例において、プライマ処
理、機械的処理、化学的処理等いわゆる1次的処
理を施してから2次的に熱可塑性樹脂を施すもの
を除いては、その密着性に問題が残り、実用上支
障が存した。そして、1次的処理をするものにあ
つては、その処理自体を要することに問題があ
り、時間的、材料的無駄が存していたのである。
特に上記方式の内では、性能上プライマ処理によ
るものが最も望ましいのではあるが、セルフロツ
キング剤組成物を施すのはねじ部材の一部である
にもかかわらず、ねじ部材全面に比較的高価なプ
ライマ処理剤を塗布しなければならず材料に無駄
が存していたことも理解されよう。さりとて、セ
ルフロツキング剤の塗布部分にのみプライマ処理
することは処理工程上困難である。 However, in the above conventional examples, except for those in which a thermoplastic resin is applied secondarily after so-called primary treatment such as primer treatment, mechanical treatment, or chemical treatment, problems remain in the adhesion. There were practical problems. For those that require primary processing, there is a problem in that the processing itself is required, resulting in waste of time and materials.
In particular, among the above methods, primer treatment is the most desirable in terms of performance, but it is relatively expensive to apply the self-locking agent composition to the entire surface of the screw member, even though it is only a part of the screw member. It is also understood that there was a waste of material as a primer treatment agent had to be applied. However, it is difficult to perform primer treatment only on the area to which the self-locking agent is applied due to the processing process.
この発明の第1の目的とするところは、プライ
マ処理を要することなく、ナイロンがねじ面にプ
ライマ処理を施したのと同等以上の接着力を発現
することのできるセルフロツキング剤組成物を得
ることにある。 The first object of the present invention is to obtain a self-locking agent composition that can exhibit an adhesive strength equivalent to or higher than that of nylon that has been subjected to primer treatment on the threaded surface without requiring primer treatment. There is a particular thing.
又、この発明の第2の目的とするところは、前
記セルフロツキング剤を専ら利用して簡易な製造
法により、ねじ部材にナイロンをより一層強固に
結合させたセルフロツキングねじ部材を提供する
ことにある。 A second object of the present invention is to provide a self-locking screw member in which nylon is more firmly bonded to the screw member by a simple manufacturing method exclusively using the self-locking agent. There is a particular thing.
上記第1の目的を達成するためのセルフロツキ
ング剤組成物は、揮発性溶媒中にポリアミド又は
及びコポリアミドの第1材料と、該第1材料を被
着ねじ面に親和させるための第2材料とを包含せ
しめて混合分散物としたことを特徴とするセルフ
ロツキンク剤組成物である。 A self-locking agent composition for achieving the above first object comprises a first material of polyamide or copolyamide in a volatile solvent, and a second material for making the first material compatible with the threaded surface. This is a self-locking agent composition characterized in that it contains the following ingredients to form a mixed dispersion.
又、上記第2の目的を達成するためのセルフロ
ツキングねじ部材は、揮発性溶媒中にポリアミド
又は及びコポリアミドの第1材料と、該第1材料
を被着ねじ面に親和させるための第2材料とを包
含せしめた混合分散溶液を、前記ねじ面の少なく
とも一部分に塗布して加熱融着させたことを特徴
とするセルフロツキングねじ部材である。 Further, the self-locking screw member for achieving the second object includes a first material of polyamide or copolyamide in a volatile solvent, and a second material for making the first material compatible with the thread surface to which it is attached. The self-locking screw member is characterized in that a mixed dispersion solution containing the two materials is applied to at least a portion of the screw surface and heat-fused.
セルフロツキング剤組成物に使用する主成分た
る第1材料のナイロンとしては、例えばナイロン
6、ナイロン6/6、ナイロン6/10、ナイロン
8、ナイロン11、ナイロン12、又はそれらの共重
合体を用いることができる。 Examples of the first material nylon used in the self-locking agent composition include nylon 6, nylon 6/6, nylon 6/10, nylon 8, nylon 11, nylon 12, or copolymers thereof. Can be used.
ナイロン種の選定に於いて考慮すべき事は、溶
融点が分解温度よりも比較的低くて複雑な熱制御
を必要とせず加工し易い事、溶融時に於いては塗
布加工形状を大きく変えない程度の粘性有し、被
着体ねじへの密着力が良い事、吸水率が小さく引
つ掻きに対する抵抗力が高く靭性、耐衝撃性に優
れている事、硬度及び強度が高く丈夫で弾力を有
する事、耐薬品性、耐摩耗性に優れ摩擦係数が小
さい事などが好ましくナイロン11乃至12又はそれ
らの共重合体が好ましく用いられるがこれらに限
定されるものではない。 Things to consider when selecting a nylon type are that the melting point is relatively lower than the decomposition temperature, making it easy to process without the need for complex heat control, and that the shape of the applied product does not change significantly during melting. viscosity, good adhesion to adherend screws, low water absorption, high resistance to scratching, excellent toughness and impact resistance, high hardness and strength, durable and elastic. In particular, nylon 11 or 12 or copolymers thereof are preferably used because they have excellent chemical resistance, abrasion resistance, and a small coefficient of friction, but are not limited to these.
使用されるナイロン粉末の粒径としては10〜
500μ、好ましくは30〜300μの範囲が良好である。 The particle size of the nylon powder used is 10~
A good range is 500μ, preferably 30 to 300μ.
ナイロンの持つ優れた特性を活かしながらセル
フロツキングネジ締付部材に効果的に適用し接着
力を強化する為に必要な第2材料としては
(A) エポキシ樹脂とフエノール樹脂よりなる組成
物
(B) エポキシ樹脂と−アミノ基、エポキシ基或い
はオキシラン基を持つ有機硅素化合物とよりな
る組成物
(C) 前記(B)項の組成物にアミノ樹脂を加えたもの
より成る組成物
(D) エポキシ樹脂とチタネートよりなる組成物等
が有効であるが特に(B)、(C)項の組成物が最適で
ある。 The second material necessary to effectively apply nylon to self-locking screw tightening members and strengthen its adhesive strength while taking advantage of the excellent properties of nylon is (A) a composition made of epoxy resin and phenolic resin (B). ) A composition comprising an epoxy resin and an organosilicon compound having an amino group, an epoxy group, or an oxirane group (C) A composition comprising an amino resin added to the composition of item (B) above (D) An epoxy resin Compositions consisting of titanate and titanate are effective, but compositions of items (B) and (C) are particularly optimal.
第2材料の組成物として用いられるエポキシ樹
脂としては、ビスフエノールA型エポキシ樹脂で
平均分子量800以上の例えば、シエル社製エピコ
ート1004、1007、1009が良好であり、平均分子量
2900のエピコート1007が最適である。 As the epoxy resin used as the composition of the second material, bisphenol A type epoxy resins having an average molecular weight of 800 or more, such as Epicoat 1004, 1007, and 1009 manufactured by Ciel Corporation, are good.
2900 Epicote 1007 is optimal.
エポキシ樹脂と配合して用いられるフエノール
系樹脂としては、フエノール樹脂、クレゾール変
性フエノール樹脂などが好ましく、その配合割合
はエポキシ樹脂/フエノール樹脂の重量比で1/
(0.5/2.0)程度の範囲が好ましい。 As the phenolic resin used in combination with the epoxy resin, phenolic resin, cresol-modified phenolic resin, etc. are preferable, and the mixing ratio is 1/1 in the weight ratio of epoxy resin/phenolic resin.
A range of about (0.5/2.0) is preferable.
又、エポキシ樹脂に添加する有機硅素化合物と
してはアミノ基を有する有機硅素化合物、例えば
γ−アミノプロピルトリエトキシシラン、N+β
アミノエチル+γアミノプロピルトリメトキシシ
ラン、γ−アミノ−プロピルトリメトキシシラン
等、又エポキシ基或いはオキシラン基を有する有
機硅素化合物、例えばγ−グリシドキシプロピル
トリメトキシシラン、γ+β−メチルグリシドキ
シ+プロピルトリメトキシシラン等が有効であ
る。 Further, as the organic silicon compound added to the epoxy resin, an organic silicon compound having an amino group, such as γ-aminopropyltriethoxysilane, N+β
Aminoethyl + γ-aminopropyltrimethoxysilane, γ-amino-propyltrimethoxysilane, etc., and organic silicon compounds having an epoxy group or oxirane group, such as γ-glycidoxypropyltrimethoxysilane, γ + β-methylglycidoxy + propyl Trimethoxysilane etc. are effective.
エポキシ樹脂に対する有機硅素化合物の添加割
合は有機硅素化合物/エポキシ樹脂の重量比で
1/(50〜2)の範囲が好ましく更には1/(20
〜5)が好ましい。 The ratio of the organosilicon compound added to the epoxy resin is preferably in the range of 1/(50 to 2) in terms of weight ratio of organosilicon compound/epoxy resin, and more preferably 1/(20
-5) are preferred.
エポキシ樹脂と配合して用いられるアミノ樹脂
は、エポキシ樹脂の硬化剤として作用し、ねじ部
材の被着面に形成される樹脂膜の強靭性を高め、
耐熱性、耐薬品性、耐摩耗性、耐候性を向上させ
る。このアミノ樹脂としては、例えばメラミン樹
脂、尿素樹脂、アニリンアルデヒド樹脂等のアミ
ノ基を含む化合物、アルデヒドの縮合反応によつ
て得られる樹脂が挙げられる。 Amino resin used in combination with epoxy resin acts as a curing agent for the epoxy resin, increasing the toughness of the resin film formed on the surface of the screw member,
Improves heat resistance, chemical resistance, abrasion resistance, and weather resistance. Examples of the amino resin include compounds containing amino groups such as melamine resins, urea resins, and aniline aldehyde resins, and resins obtained by condensation reactions of aldehydes.
また、エポキシ樹脂と配合して用いられるイソ
シアネートは、本発明のセルフロツキング剤がね
じ部材に塗布されてねじ部材の被着面に加熱硬化
される際に、エポキシ樹脂の硬化剤、架橋剤とし
て作用し、被着面及びナイロンに対する密着性を
高めると共に、ねじ部材に形成された樹脂膜の強
靭性を高め、ねじ部材の螺進時に生じる樹脂膜の
損傷、剥落を防止する。従つて、本発明において
用いられるイソシアネートは、このような作用を
有し、エポキシ樹脂を介して粉状ナイロンを被着
ねじ面に加熱融着させ得るものであれば良く、特
に限定されない。このイソシアネートは、イソシ
アネート系化合物、ブロツクイソシアネート系化
合物等であり、好ましくは、トリレンジイソシア
ネート、ヘキサメチレンジイソシアネート等のブ
ロツクイソシアネート系化合物である。トリレン
ジイソシアネートの具体例としては、コロネート
APステイープル(日本ポリウレタン工業(株)製、
商品名)がある。更に、イソシアネートの配合割
合は、エポキシ樹脂/イソシアネートの重量比で
5/(1〜5)の範囲が好ましい。 In addition, the isocyanate used in combination with the epoxy resin acts as a curing agent and a crosslinking agent for the epoxy resin when the self-locking agent of the present invention is applied to the screw member and hardened by heating on the surface to which the screw member is attached. This increases the adhesion to the surface to be adhered to and the nylon, and also increases the toughness of the resin film formed on the screw member, thereby preventing the resin film from being damaged or peeled off when the screw member is threaded. Therefore, the isocyanate used in the present invention is not particularly limited as long as it has such an effect and can heat-fuse the powdered nylon to the threaded surface via the epoxy resin. The isocyanate includes an isocyanate compound, a blocked isocyanate compound, and preferably a blocked isocyanate compound such as tolylene diisocyanate and hexamethylene diisocyanate. A specific example of tolylene diisocyanate is coronate.
AP staple (manufactured by Nippon Polyurethane Industries Co., Ltd.)
There is a product name). Furthermore, the blending ratio of isocyanate is preferably in the range of 5/(1 to 5) in weight ratio of epoxy resin/isocyanate.
エポキシ樹脂と配合して用いられるチタネート
は、テトラアルコキシチタン化合物、チタニウム
系カツプリング剤等であり、好ましくは、イソプ
ロピルトリ(N−アミノエチルアミノ)チタネー
ト、ジイソプロピル(ジオクチルパイロホスフエ
ート)チタネート、テトラジオクチルビス(ジト
リデシルホスフアイト)チタネート、テトラ
(2.2−ジアリルオキシメチル−1−ブチル)ビス
(ジトリデシル)チタネート等が挙げられる。こ
のチタネートの配合割合は、エポキシ樹脂/チタ
ネートの重量比で1/(1〜5)が好ましい。 The titanate used in combination with the epoxy resin is a tetraalkoxy titanium compound, a titanium-based coupling agent, etc., and preferably isopropyl tri(N-aminoethylamino) titanate, diisopropyl (dioctyl pyrophosphate) titanate, tetradioctyl bis (ditridecyl phosphite) titanate, tetra(2.2-diallyloxymethyl-1-butyl)bis(ditridecyl) titanate, and the like. The blending ratio of this titanate is preferably 1/(1 to 5) in weight ratio of epoxy resin/titanate.
セルフロツキング剤組成物に使用する揮発性溶
媒としては例えばベンゼン、トルエン、キシレン
等の芳香族系溶剤、1.2.4.トリクロロエチレン、
1.1.1.トリクロロエタン等の塩素系溶剤、アセト
ン、メチルエチルケトン等のケトン系溶剤等を用
いることができるが、要するに上記第1材料と第
2材料とを分散する溶媒であればよく、好ましく
は第2材料が溶解する溶媒の使用が望ましい。上
記例に限定されるものではない。 Examples of volatile solvents used in the self-locking agent composition include aromatic solvents such as benzene, toluene, and xylene; 1.2.4. trichloroethylene;
1.1.1. Chlorinated solvents such as trichloroethane, ketone solvents such as acetone and methyl ethyl ketone, etc. can be used, but in short, any solvent that can disperse the first material and the second material may be used, preferably the second material. It is desirable to use a solvent in which the material is soluble. It is not limited to the above example.
セルフロツキング剤組成物は、第1材料と第2
材料とを揮発性溶媒中に分散せしめて得られる。
このようにして得られたセルフロツキング剤組成
物を被着体に塗布し、揮発性溶媒の乾燥と同時、
又は乾燥後加熱すれば、被着体にプライマ処理し
たのと同様の第2材料による処理面が形成され、
被着体に第1材料たるナイロンが強固に接着する
のである。 The self-locking agent composition includes a first material and a second material.
It is obtained by dispersing the material in a volatile solvent.
The self-locking agent composition thus obtained is applied to an adherend, and at the same time as the volatile solvent is dried,
Alternatively, by heating after drying, a treated surface of the second material similar to that treated with the primer is formed on the adherend,
The first material, nylon, firmly adheres to the adherend.
第1図〜第4図にねじ部材としてボルトの例を
挙げ、セルフロツキングねじ部材の適用例を示し
た。第1図は六角穴付ボルト1のねじ部3の一部
に楕円形状のセルフロツキング剤組成物5を塗布
したものである。第2図はボルト7に同じくセル
フロツキング剤組成物5を施したものである。第
3図は止めねじ9のねじ部3に全周に亘つて帯状
にセルフロツキング剤組成物5を施したものであ
る。第4図は六角穴付ボルト1に第3図のものと
同じく帯状にセルフロツキング剤組成物を施した
ものである。 1 to 4 show an example of a bolt as a screw member and an application example of a self-locking screw member. FIG. 1 shows an elliptical self-locking agent composition 5 coated on a part of the threaded portion 3 of a hexagon socket head bolt 1. As shown in FIG. FIG. 2 shows a bolt 7 similarly coated with the self-locking agent composition 5. In FIG. 3, a self-locking agent composition 5 is applied in a band-like manner to the threaded portion 3 of a set screw 9 over the entire circumference. FIG. 4 shows a hexagonal socket bolt 1 coated with a self-locking agent composition in the form of a band, similar to that shown in FIG.
前処理としてはトリクロルエチレン等による脱
脂作業のみで十分である。又、ボルト自体の素材
としては、鉄、銅、真ちゆう、ステンレス等の
他、クロム、亜鉛、クロメート、ニツケル等メツ
キ処理されているものであつてよい。 As pretreatment, degreasing with trichlorethylene or the like is sufficient. The material of the bolt itself may be iron, copper, brass, stainless steel, etc., as well as plated materials such as chromium, zinc, chromate, nickel, etc.
第1図〜第4図に示したように、ねじ部材に所
定のセルフロツキング剤組成物を施した後、乾燥
と同時、又は乾燥後に加熱融着させる。融着させ
た後のセルフロツキング剤組成物を参照番号11
で示す。第5図にセルフロツク機能の例を示し
た。これは、ねじ部にセルフロツキング剤を施し
たボルト7を母材13の雌ねじに螺入させて板材
15を固定している状態である。セルフロツキン
グ剤11により強固にセルフロツクされている。
第6図は止めビス17を母材の雌ねじに螺入し、
ビス先端でレバ19の位置をバネ21の力に抗し
て調整位置決めしている状態を示す。第7図はシ
ーリング効果の例を示すもので、容器(例えばオ
イル容器)23の底面に全周に帯状にセルフロツ
キング剤11を施設した六角穴付ボルト1を螺入
し、オイル等液体のシーリング効果を果している
例である。液体に限定されるものではなく空気等
流体にも勿論適用できる。又、第7図に示される
ことからも理解されるように例えば水道蛇口等の
ねじ部に、常用されているシールテープに代えて
セルフロツキング剤組成物を適用することもでき
る。 As shown in FIGS. 1 to 4, after a predetermined self-locking agent composition is applied to a screw member, it is heat-fused either simultaneously with drying or after drying. The self-locking agent composition after fusing is shown in reference number 11.
Indicated by Figure 5 shows an example of the self-lock function. In this state, the plate material 15 is fixed by screwing the bolt 7, whose threaded portion is coated with a self-locking agent, into the female thread of the base material 13. It is strongly self-locked by the self-locking agent 11.
Figure 6 shows that the set screw 17 is screwed into the female thread of the base material.
The state in which the lever 19 is adjusted and positioned at the tip of the screw against the force of the spring 21 is shown. FIG. 7 shows an example of the sealing effect, in which a hexagon socket head bolt 1 with a self-locking agent 11 applied in a strip around the entire circumference is screwed into the bottom of a container (for example, an oil container) 23, and a liquid such as oil is removed. This is an example of a sealing effect. It is of course applicable not only to liquids but also to fluids such as air. Furthermore, as can be seen from FIG. 7, the self-locking agent composition can be applied to the threaded portion of a water faucet, for example, in place of the commonly used sealing tape.
実施例 1
溶媒メチルエチルケトン中に第1成分としてナ
イロン11を100重量部、エポキシ樹脂5重量部、
イソシアネート(コロネートAPステイープル)
3重量部を分散させ、金属面間に充填乾燥後、
220℃で30分加熱融着せしめて、剪断接着力を試
験した。この結果、ナイロン成分のみを分散させ
たものの剪断接着力が平均値で217Kg/cmであつ
たのに比べ、平均値341Kg/cmであつた。Example 1 In the solvent methyl ethyl ketone, 100 parts by weight of nylon 11 as the first component, 5 parts by weight of epoxy resin,
Isocyanate (Coronate AP Staple)
After dispersing 3 parts by weight and filling between metal surfaces and drying,
The shear adhesive strength was tested by heating and fusing at 220°C for 30 minutes. As a result, the average shear adhesive strength was 341 kg/cm, compared to the average value of 217 kg/cm when only the nylon component was dispersed.
実施例 2
M8×JIS2級ボルト、クロムメツキ品をトリク
ロルエチレンで脱脂後、日本リルサン社製ナイロ
ン−11:シエルエピコート1007:イソシアネート
APステイープルを100:5:3の重量割合で溶媒
中に分散せしめて得られた組成物をねじ面へ付着
させ、風乾後、220℃で30分加熱してねじ面に効
果的に沈着せしめて融着させセルフロツキングね
じ部材を得た。Example 2 After degreasing M8 x JIS 2nd class bolt, chrome plated product with trichlorethylene, Nippon Rilsan Co., Ltd. nylon-11: Ciel Epicote 1007: Isocyanate
The composition obtained by dispersing AP staples in a solvent at a weight ratio of 100:5:3 was applied to the threaded surface, and after air-drying, the composition was heated at 220°C for 30 minutes to effectively deposit it on the threaded surface. A self-locking screw member was obtained by fusion bonding.
上記セルフロツキングねじ部材を雌ナツト部材
にねじ込み、締付け方向及び戻し方向へのトルク
強度を測定したところ、第1回目〜5回目の締付
強度平均値は55、40、30、25、20(Kg・cm)であ
つた。そして戻しトルクは同じく、50、37、28、
22、18であつた。JASO(F−106−74:自動車用
ゆるみ止め六角ナツト)規格に準じた5回以上の
繰り返し使用が可能である。 When the above self-locking screw member was screwed into the female nut member and the torque strength in the tightening direction and return direction was measured, the average value of the tightening strength for the first to fifth times was 55, 40, 30, 25, 20 ( Kg・cm). And the return torque is the same, 50, 37, 28,
It was 22 and 18. It can be used repeatedly more than 5 times in accordance with the JASO (F-106-74: Automotive locking hexagon nut) standard.
なお、耐熱耐寒性については−50℃〜120℃の
範囲で十分使用可能であつた。耐薬品性耐候性に
ついてはナイロン自体の特性に準じるものであ
る。 In addition, regarding heat and cold resistance, it was sufficiently usable in the range of -50°C to 120°C. Chemical resistance and weather resistance are based on the characteristics of nylon itself.
セルフロツクねじ部材としては自動車、オート
バイ、自転車、車輌、家庭用電気機器、住宅機
器、通信機、ミシン、メガネ、油圧・空圧機器、
農業機械、建設機械、造船、包装機械、水道部品
その他の機械、装置類の各種ねじに適用できる。 Self-locking screw parts are used in automobiles, motorcycles, bicycles, vehicles, household electrical equipment, housing equipment, communications equipment, sewing machines, eyeglasses, hydraulic and pneumatic equipment,
Applicable to various screws for agricultural machinery, construction machinery, shipbuilding, packaging machinery, water supply parts, and other machinery and equipment.
揮発性溶媒中にポリアミド又は及びコポリアミ
ドの第1材料と、該第1材料を被着ねじ面に親和
させるための第2材料とを包含せしめて混合分散
物としたことを特徴とするこの発明に係るセルフ
ロツキンク剤組成物は、プライマ処理を要するこ
となく、ナイロンがねじ面にプライマ処理を施し
たの同等以上の接着力を発現することができる。 This invention is characterized in that a first material of polyamide or copolyamide and a second material for making the first material compatible with the threaded surface to be adhered are included in a volatile solvent to form a mixed dispersion. The self-locking agent composition according to the above is capable of exhibiting an adhesive force equivalent to or higher than that of nylon that has been subjected to a primer treatment on the threaded surface, without requiring a primer treatment.
揮発性溶媒中にポリアミド又は及びコポリアミ
ドの第1材料と、該該1材料を被着ねじ面に親和
させるための第2材料とを包含せしめた混合分散
溶液を、前記ねじ面の少なくとも一部分に塗布し
て加熱融着させたことを特徴とするセルフロツキ
ングねじ部材は、前記セルフロツキング剤組成物
を専ら利用して簡易な製造法であり、ねじ部材に
ナイロンをより一層強固に結合させたセルフロツ
キング部材を提供することができる。 A mixed dispersion solution containing a first material of polyamide or copolyamide in a volatile solvent and a second material for making the first material compatible with the threaded surface is applied to at least a portion of the threaded surface. The self-locking screw member, which is characterized by being coated and heat-fused, is a simple manufacturing method that exclusively uses the self-locking agent composition, and it is possible to bond nylon to the screw member even more firmly. A self-locking member can be provided.
図面はいずれも実施例を示し、第1図は六角穴
付ボルトのねじ部の一部分に楕円形状のセルフロ
ツキング剤組成物を施した側面図、第2図は六角
ボルトのねじ部の一部分に楕円形状のセルフロツ
キング剤組成物を施した側面図、第3図は止めね
じに全周帯状にセルフロツキング剤組成物を施し
た側面図、第4図は六角穴付ボルトのねじ部全周
帯状にセルフロツキング剤組成物を施した側面図
である。第5図はセルフロツクの状態を図におい
て左半分を断面図で示す側面図、第6図は止めビ
スの位置調整(アジヤスト)状態を説明する一部
切欠断面側面図、第7図は流体のシーリング効果
を説明する断面図である。
5……セルフロツキング剤組成物(塗布状態)、
11……セルフロツキング剤組成物(加熱融着状
態)。
The drawings all show examples; Fig. 1 is a side view of a part of the threaded part of a hexagon socket head cap screw with an elliptical self-locking agent composition applied thereto, and Fig. 2 is a side view of a part of the threaded part of a hexagonal socket head cap screw coated with the self-locking agent composition. Fig. 3 is a side view showing a self-locking agent composition applied to an oval-shaped self-locking agent composition, Fig. 3 is a side view showing a self-locking agent composition applied to a set screw in the form of a band around the entire circumference, and Fig. 4 is a side view showing the entire threaded part of a hexagon socket head bolt. FIG. 3 is a side view showing a self-locking agent composition applied in a circumferential band. Fig. 5 is a side view showing the self-locking state with a sectional view of the left half of the figure, Fig. 6 is a partially cutaway sectional side view illustrating the setting screw position adjustment (adjustment) state, and Fig. 7 is the fluid sealing. It is a sectional view explaining an effect. 5...Self-locking agent composition (applied state),
11...Self-locking agent composition (heat-fused state).
Claims (1)
ド又は及びコポリアミド粉末の第1材料と、該第
1材料を被着ねじ面に親和させるためのエポキシ
樹脂からなる第2材料を混合し、前記第1材料は
前記揮発性溶媒中に分散させ、また前記第2材料
は前記揮発性溶媒中に溶解させて混合分散液状の
組成物とし、該組成物をねじ部を有する被着体の
ねじ面の少なくとも一部に塗布し、該組成物の揮
発性溶媒を揮散させ、加熱融着させることを特徴
とするセルフロツキングねじ部材の製造方法。1. Mix a first material of polyamide or copolyamide powder with a particle size of 10 to 500 μm in a volatile solvent, and a second material of epoxy resin to make the first material compatible with the threaded surface, and The first material is dispersed in the volatile solvent, and the second material is dissolved in the volatile solvent to form a mixed and dispersed liquid composition, and the composition is applied to the threaded surface of an adherend having a threaded part. 1. A method for producing a self-locking screw member, which comprises coating at least a portion of the composition, volatilizing the volatile solvent of the composition, and heat-sealing the composition.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59041934A JPS60188609A (en) | 1984-03-07 | 1984-03-07 | Self-locking agent composition and self-locking screw member |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59041934A JPS60188609A (en) | 1984-03-07 | 1984-03-07 | Self-locking agent composition and self-locking screw member |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60188609A JPS60188609A (en) | 1985-09-26 |
JPH0420093B2 true JPH0420093B2 (en) | 1992-03-31 |
Family
ID=12622055
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59041934A Granted JPS60188609A (en) | 1984-03-07 | 1984-03-07 | Self-locking agent composition and self-locking screw member |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60188609A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE60220532T2 (en) * | 2001-10-26 | 2008-02-07 | Three Bond Co., Ltd., Tokio/Tokyo | COMPOSITION FOR USE AS SELF-BLOCKING AGENT AND THIS USING SELF-BLOCKING LINK |
JP6735015B2 (en) * | 2015-12-16 | 2020-08-05 | 株式会社スリーボンド | Coating film forming resin composition |
JP6652474B2 (en) * | 2016-09-29 | 2020-02-26 | 日立オートモティブシステムズ株式会社 | Electronic control unit |
JP7125307B2 (en) * | 2018-08-30 | 2022-08-24 | ポリプラ・エボニック株式会社 | Curable resin composition, composite member and manufacturing method thereof |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5754186A (en) * | 1980-08-15 | 1982-03-31 | Ciba Geigy | |
JPS588907A (en) * | 1981-07-08 | 1983-01-19 | Shinsaku Goto | Burner for bath boiler |
-
1984
- 1984-03-07 JP JP59041934A patent/JPS60188609A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5754186A (en) * | 1980-08-15 | 1982-03-31 | Ciba Geigy | |
JPS588907A (en) * | 1981-07-08 | 1983-01-19 | Shinsaku Goto | Burner for bath boiler |
Also Published As
Publication number | Publication date |
---|---|
JPS60188609A (en) | 1985-09-26 |
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