JP2007332269A5 - - Google Patents
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- JP2007332269A5 JP2007332269A5 JP2006165644A JP2006165644A JP2007332269A5 JP 2007332269 A5 JP2007332269 A5 JP 2007332269A5 JP 2006165644 A JP2006165644 A JP 2006165644A JP 2006165644 A JP2006165644 A JP 2006165644A JP 2007332269 A5 JP2007332269 A5 JP 2007332269A5
- Authority
- JP
- Japan
- Prior art keywords
- polymerization method
- particle size
- isocyanate group
- polybutadiene
- larger
- 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.)
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- 239000011248 coating agent Substances 0.000 claims description 5
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 4
- 229920002589 poly(vinylethylene) polymer Polymers 0.000 claims description 2
- 229920005668 polycarbonate resin Polymers 0.000 claims 1
- 239000004431 polycarbonate resin Substances 0.000 claims 1
- 239000002245 particle Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 4
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 238000010556 emulsion polymerization method Methods 0.000 description 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 238000010558 suspension polymerization method Methods 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 1
- 229920001228 Polyisocyanate Polymers 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- DVQHRBFGRZHMSR-NWBUNABESA-N sodium;methyl 2,2-dimethyl-4,6-dioxo-5-[(E)-N-prop-2-enoxy-C-propylcarbonimidoyl]cyclohexane-1-carboxylate Chemical compound [Na+].C=CCO\N=C(/CCC)[C-]1C(=O)CC(C)(C)C(C(=O)OC)C1=O DVQHRBFGRZHMSR-NWBUNABESA-N 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
Description
これらのフッ素系樹脂の粒子は、塊状重合法、懸濁重合法、溶液重合法、乳化重合法などで得られたフッ素樹脂を粒子径0.1〜5μm程度に分級したものや、懸濁重合法、溶液重合法、乳化重合法などで得られた分散液をせん断攪拌などにより、0.1〜5μm程度に微粒子分散させたもの、これらの重合法で得られたものを凝析・乾操後、乾式粉砕や冷却粉砕により、10μm以下に微粒子化したものなどが用いられる。0.1〜10μmに設定される粒子径において、粒子径がより小さい場合には、塗布厚みを小さく出来るメリットがあるが、塗布表面の凹凸が小さくなることにより接触面積が小さくなり、低面圧では摩擦係数が大きくなる傾向があり、一方粒子径がより大きい場合には、塗布厚みが大きくなり、塗布の際のコストがかかるが、凹凸が大きくなり、低面圧では相手材との接触面積が小さくなり、摩擦係数が下がるようになる。したがって、粒子径は使用要求によって適宜調整され、例えばシール部品などではこれら長所、短所を考慮して決定され、好ましくは0.5〜2μm程度のものが用いられる。 These fluororesin particles are obtained by classifying a fluororesin obtained by a bulk polymerization method , a suspension polymerization method , a solution polymerization method , an emulsion polymerization method or the like into a particle size of about 0.1 to 5 μm, a suspension polymerization method , Dispersions obtained by solution polymerization method , emulsion polymerization method, etc. are dispersed in fine particles to about 0.1-5μm by shearing stirring, etc., and those obtained by these polymerization methods are coagulated and dried, then dry pulverized by and cooling grinding, such as those micronized is used to 10μm or less. When the particle size is set to 0.1 to 10 μm, if the particle size is smaller, there is an advantage that the coating thickness can be reduced, but the contact area becomes smaller due to the unevenness of the coating surface being reduced, and friction at low surface pressures When the particle size is larger, on the other hand, when the particle size is larger, the coating thickness becomes larger and the cost for coating increases, but the unevenness becomes larger and the contact area with the counterpart material becomes smaller at low surface pressure. Thus, the friction coefficient is lowered. Therefore, the particle diameter is appropriately adjusted according to the usage requirements, and for example, seal parts are determined in consideration of these advantages and disadvantages, and those having a particle size of about 0.5 to 2 μm are preferably used.
イソシアネート基含有1,2-ポリブタジエンとしては、末端基としてイソシアネート基が付加された分子量1,000〜3,000程度のものが用いられ、これは市販品、例えば日本曹達製品日曹TP-1001(酢酸ブチル50重量%含有溶液)などをそのまま用いることが出来る。このポリブタジエン樹脂は、同様のイソシアネート基で反応高分子化するポリイソシアネート樹脂よりも、ゴムとの相性、相溶性が良いため、ゴムとの密着性が良く、特に耐摩擦・摩耗特性が良いのが特徴である。 As the isocyanate group-containing 1,2-polybutadiene, a molecular weight of about 1,000 to 3,000 with an isocyanate group added as a terminal group is used, which is a commercial product such as Nippon Soda product Nisso TP-1001 (butyl acetate 50 wt. % -Containing solution) can be used as they are. This polybutadiene resin has better compatibility and compatibility with rubber than polyisocyanate resin that reacts with the same isocyanate group to polymerize, so it has good adhesion to rubber, and particularly good friction and wear characteristics. It is a feature.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006165644A JP4992309B2 (en) | 2006-06-15 | 2006-06-15 | Rubbery elastic coating agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006165644A JP4992309B2 (en) | 2006-06-15 | 2006-06-15 | Rubbery elastic coating agent |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2007332269A JP2007332269A (en) | 2007-12-27 |
JP2007332269A5 true JP2007332269A5 (en) | 2009-07-16 |
JP4992309B2 JP4992309B2 (en) | 2012-08-08 |
Family
ID=38932042
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2006165644A Expired - Fee Related JP4992309B2 (en) | 2006-06-15 | 2006-06-15 | Rubbery elastic coating agent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP4992309B2 (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102013203194A1 (en) * | 2013-02-27 | 2014-08-28 | Robert Bosch Gmbh | Dispersion-coated squeegee |
US10190014B2 (en) | 2014-09-22 | 2019-01-29 | Nok Corporation | Surface-treating agent for vulcanized rubber |
EP3199583B1 (en) | 2014-09-22 | 2019-01-09 | NOK Corporation | Surface treatment agent for vulcanized rubber |
CN107250299B (en) * | 2015-02-17 | 2019-11-19 | Nok株式会社 | Oil sealing coating agent |
WO2021014902A1 (en) * | 2019-07-25 | 2021-01-28 | Nok株式会社 | Coating agent for oil seal |
WO2021014901A1 (en) * | 2019-07-25 | 2021-01-28 | Nok株式会社 | Coating agent for oil seal |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3104545B2 (en) * | 1993-09-10 | 2000-10-30 | 信越化学工業株式会社 | Organopolysiloxane composition and rubber part |
JP3893985B2 (en) * | 2002-01-22 | 2007-03-14 | Nok株式会社 | Surface treatment agent for vulcanized rubber |
-
2006
- 2006-06-15 JP JP2006165644A patent/JP4992309B2/en not_active Expired - Fee Related
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