JPS6234360B2 - - Google Patents
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- Publication number
- JPS6234360B2 JPS6234360B2 JP57118656A JP11865682A JPS6234360B2 JP S6234360 B2 JPS6234360 B2 JP S6234360B2 JP 57118656 A JP57118656 A JP 57118656A JP 11865682 A JP11865682 A JP 11865682A JP S6234360 B2 JPS6234360 B2 JP S6234360B2
- Authority
- JP
- Japan
- Prior art keywords
- water
- weight
- film
- polymer
- lubricant 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
Links
- 239000000314 lubricant Substances 0.000 claims description 27
- 239000000203 mixture Substances 0.000 claims description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- 229920000642 polymer Polymers 0.000 claims description 15
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 13
- 239000006185 dispersion Substances 0.000 claims description 10
- 229920001059 synthetic polymer Polymers 0.000 claims description 10
- 241000196324 Embryophyta Species 0.000 claims description 9
- 229920002472 Starch Polymers 0.000 claims description 9
- 239000008107 starch Substances 0.000 claims description 9
- 235000019698 starch Nutrition 0.000 claims description 9
- 235000013311 vegetables Nutrition 0.000 claims description 5
- 229920000856 Amylose Polymers 0.000 claims description 4
- 229920000945 Amylopectin Polymers 0.000 claims description 3
- 229920001353 Dextrin Polymers 0.000 claims description 3
- 239000004375 Dextrin Substances 0.000 claims description 3
- 239000002202 Polyethylene glycol Substances 0.000 claims description 3
- 229920000180 alkyd Polymers 0.000 claims description 3
- 235000019425 dextrin Nutrition 0.000 claims description 3
- 239000005011 phenolic resin Substances 0.000 claims description 3
- 229920001225 polyester resin Polymers 0.000 claims description 3
- 239000004645 polyester resin Substances 0.000 claims description 3
- 229920001223 polyethylene glycol Polymers 0.000 claims description 3
- 229920002907 Guar gum Polymers 0.000 claims description 2
- -1 derivatives thereof Polymers 0.000 claims description 2
- 239000000665 guar gum Substances 0.000 claims description 2
- 235000010417 guar gum Nutrition 0.000 claims description 2
- 229960002154 guar gum Drugs 0.000 claims description 2
- 229920001568 phenolic resin Polymers 0.000 claims description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims 1
- 239000003822 epoxy resin Substances 0.000 claims 1
- 239000005038 ethylene vinyl acetate Substances 0.000 claims 1
- 229920000647 polyepoxide Polymers 0.000 claims 1
- 239000011248 coating agent Substances 0.000 description 10
- 238000000576 coating method Methods 0.000 description 10
- 230000001050 lubricating effect Effects 0.000 description 9
- 239000007787 solid Substances 0.000 description 8
- 238000005461 lubrication Methods 0.000 description 7
- 239000007788 liquid Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000004850 liquid epoxy resins (LERs) Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229920000881 Modified starch Polymers 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 235000019426 modified starch Nutrition 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- DZKDPOPGYFUOGI-UHFFFAOYSA-N tungsten(iv) oxide Chemical compound O=[W]=O DZKDPOPGYFUOGI-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920002085 Dialdehyde starch Polymers 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 239000004368 Modified starch Substances 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229920007962 Styrene Methyl Methacrylate Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 229910052936 alkali metal sulfate Inorganic materials 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- QHZOMAXECYYXGP-UHFFFAOYSA-N ethene;prop-2-enoic acid Chemical group C=C.OC(=O)C=C QHZOMAXECYYXGP-UHFFFAOYSA-N 0.000 description 1
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 229920000591 gum Polymers 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- ADFPJHOAARPYLP-UHFFFAOYSA-N methyl 2-methylprop-2-enoate;styrene Chemical compound COC(=O)C(C)=C.C=CC1=CC=CC=C1 ADFPJHOAARPYLP-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 239000001254 oxidized starch Substances 0.000 description 1
- 235000013808 oxidized starch Nutrition 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- XWNXEWLCHSLQOI-UHFFFAOYSA-K trisodium;triacetate Chemical compound [Na+].[Na+].[Na+].CC([O-])=O.CC([O-])=O.CC([O-])=O XWNXEWLCHSLQOI-UHFFFAOYSA-K 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 239000012991 xanthate Substances 0.000 description 1
Landscapes
- Lubricants (AREA)
Description
この発明は、鉄の圧延、鍛造あるいは引抜き、
アルミニウムが銅の押出し、タングステンやモリ
ブデンの引抜き等、各種の金属や合金の熱間加工
の際に使用される被膜形成型高温用潤滑剤組成物
に関する。
従来、この種の潤滑剤組成物としては、潤滑
油、グリース又はこれらに黒鉛粉末や二酸化タン
グステン等の固体潤滑剤を混合したもの、あるい
は、アルカリ金属硫酸塩、ホウ酸塩、塩化カリウ
ム、ナトリウムトリアセテート、黒鉛粉末及び必
要により添加される助剤とからなる微粉末混合物
を水性分散液としたもの等が知られている。しか
しながら、前者においては、熱的に不安定であつ
て使用の際に油の分解が起り、工具や加工物に悪
影響を与えるほか、油や油の分解物が作業環境を
著るしく汚染するという問題があり、また、後者
においては、前者の如き問題はないが、特にシー
ムレス鋼管の製造等において満足し得る潤滑性能
を発揮するとは言えないものであつた。
そこで、本発明者等は、かかる従来の潤滑剤組
成物における問題点を解消し得るものとして、先
に、黒鉛粉末と水に溶解又は分散し得る植物系高
分子とを主体とした高温用潤滑剤組成物を提案し
た(特願昭56−147297号)。この潤滑剤組成物
は、作業環境を汚染することがなく、しかも高温
において優れた潤滑性能を発揮するという点で一
応の成果を達成したが、金属表面に形成される潤
滑塗膜の耐水性が悪く、このため、作業現場にお
いては潤滑塗膜にロール冷却水等の漏水がかから
ないようにしなければならず、また、誤つて漏水
がかかると簡単に潤滑塗膜が流れ落ちたり、剥れ
たり、あるいはその塗膜厚にむらを生じたりして
その潤滑性能が悪化し、極めて使用しづらいとい
う問題があつた。
本発明は、かかる観点に鑑みて発明されたもの
であり、植物系高分子を主体とすることにより黒
鉛、樹脂及び水の一体化を図つて塗膜の形成性、
作業性を維持すると共に、合成高分子を併用する
ことにより被塗材とのなじみ性を向上させてより
良い性能を発揮し、しかも、耐水性にも優れた塗
膜を形成する高温用潤滑剤組成物を提供するもの
である。
すなわち、本発明は、黒鉛粉末50〜94重量%
と、水溶性又は水分性植物系高分子9〜40重量%
とを主体とし、これにさらに水溶性又は水分性植
物系高分子1〜20重量%をを含有し、水中に分散
させて潤滑剤水分散液として使用する被膜形成型
高温用潤滑剤組成物である。
この発明において使用される黒鉛粉末は、それ
が天然品であつてもまた合成品であつてもよい。
また、この黒鉛粉末の粒径については、通常、
100μ以下の平均粒度と少くとも75%の純度を有
するものが使用され、このうち平均粒度0.3〜30
μのものが好ましい。
また、水溶性又は水分散性植物系高分子の例と
しては、デンプン及びメチルデンプン、エチルデ
ンプン、アセチルデンプン、アリルデンプン、カ
ルボキシメチルデンプン、ジアルデヒドデンプ
ン、酸化デンプン、化工デンプン等のデンプン誘
導体、アミロース及びアミロペクチン並びにアミ
ローストリアセタート等のその誘導体、デキスト
リン及びその誘導体、寒天、及びセルロースエー
テル、カルボキシメチルセルロース、セルロース
ザンテート等のセルロース誘導体、ポリサツカラ
イド、アラビアゴム、グアーガム等の多糖類並び
にガム質等を挙げることができる。デンプン、ア
ミロース、アミロペクチン、デキストリン、及び
これらの誘導体からなるデンプン系は塗膜形成能
からみて特に好ましい。これら植物系高分子は、
単独で用いてもよく、また、二種以上を組合せて
用いてもよい。
さらに、本発明において使用される水溶性又は
水分散性合成高分子の例としては、液状エポキシ
樹脂、液状フエノール樹脂、液状シリコーン樹
脂、液状アルキド樹脂、ポリエチレングリコー
ル、ポリエチレンオキシド、ポリプロピレンオキ
シド、水溶性変性ポリエステル樹脂、アクリル酸
−アクリル酸ブチル共重合体やアクリル酸−エチ
レン共重合体のようなアクリル系樹脂、スチレン
−メチルメタクリレート共重合体のようなスチレ
ン系樹脂、エチレン−酢酸ビニル共重合体のよう
な酢酸ビニル系樹脂、液状ポリイソブチレン等を
挙げることができる。また、これらのうち好まし
いものとしては、液状エポキシ樹脂、液状フエノ
ール樹脂、ポリエチレングリコール、エチレン−
酢酸ビニル共重合体、液状アルキド樹脂、及び変
性ポリエステル樹脂等を挙げることができる。液
状エポキシ樹脂の如き単独では水に分散しないよ
うな樹脂でも本系のような黒鉛懸濁溶液中で均一
に分散し得ることができるものも本発明における
水分散性合成高分子の範疇に入る。
また、本発明において、植物系高分子は長期間
放置されると腐敗するものもあり、ホルムアルデ
ヒド、パラオキシ安息香酸エチル等の防腐剤を配
合することが好ましい。
本発明の被膜形成型高温用潤滑剤組成物の配合
割合は、通常、黒鉛粉末50〜90重量%、植物系高
分子9〜40重量%及び合成高分子1〜20重量%で
あり、好ましくは、黒鉛粉末60〜85重量%、植物
系高分子10〜30重量%及び合成高分子3〜10重量
%がよい。黒鉛粉末が50重量%より少ないと所望
の潤滑性能が得られず、90重量%より多いと被膜
強度が不十分で所望の潤滑性能が得られない。ま
た、植物系高分子が9重量%より少ないと被膜の
均一性に劣り、40重量%より多いと被膜強度が劣
り潤滑性能が落ちる。さらに、合成高分子が1重
量%より少ないと耐水性に劣り、20重量%より多
いと被膜強度が強いものの所望の潤滑性能が得ら
れない。
本発明の高温用潤滑剤組成物は、水中に分散剤
させて潤滑剤水分散液として使用するものであ
り、この使用時の固形分濃度は通常5〜35重量
%、好ましくは10〜30重量%の範囲内に調製す
る。なお、この固形分濃度の調製は、例えば一旦
固形分濃度35〜50重量%に調製しておき、使用時
に薄めて固形分濃度5〜35重量%にすることもで
きる。この固形分濃度は、薄すぎると乾燥時間が
長くなつたり形成される塗膜の膜厚が薄くなつて
良好な潤滑性能を得ることができず、また、濃す
ぎると塗布しにくくなる。このようにして調製さ
れた潤滑剤水分散液の使用方法は、この潤滑剤水
分散液を熱間加工すべき金属の表面や、マンドレ
ル、ダイス、ロール等の工具の表面に通常の手段
で塗布し、これを乾燥させてこれら金属や工具の
表面に被膜を形成した後熱間加工を行う。
なお、本発明の被膜形成型高温用潤滑剤組成物
において、その組成物中に予め、あるいは、潤滑
剤水分散液を調製する際に、従来公知の第三成
分、例えば被膜安定剤、さび止め剤、酸化防止
剤、界面活性剤、乳化剤、極圧剤等を添加し、こ
れら添加剤によつてそれぞれの特徴を付与するこ
ともできる。
本発明によれば、植物系高分子に加えて合成高
分子を併用することにより、金属表面に形成され
る潤滑塗膜の潤滑性能を高め、かつ、その耐水性
を向上させることもでき、その取扱いが極めて容
易である。
以下、本発明を実施例及び比較例に基づいて具
体的に説明する。
実施例1〜8及び比較例1〜3
表に示す割合で黒鉛粉末、植物系高分子及び合
成高分子を配合して潤滑剤組成物を調製した。
各実施例及び各比較例の潤滑剤組成物をそれぞ
れ固形分濃度23重量%となるように水に分散させ
て潤滑剤水分散液を調製し、この潤滑剤水分散液
を200℃に加熱した試験片(材質:SKD−61)上
にスプレー塗布し、試験片の表面に膜厚60μの潤
滑塗膜を形成した。
この試験片を摩擦摩耗試験機に固定し、この試
験片に0.2Kgf/mm2及び19.5Kgf/mm2の潤滑面圧
力(摺動面圧力)で圧接しながら回転する被圧延
回転試験片温度を1000℃区とし、相対摺動速度
1.5m/sの条件下における摩擦係数を求めた。
また、各実施例及び各比較例の潤滑剤組成物に
ついて調製した潤滑剤水分散液を200℃に加熱し
た50mmφ×150mmのSUS製丸棒にスプレー塗布
し、その10秒後に水道水をかける方法で形成され
た潤滑塗膜の耐水性を調べた。
結果は表に示す通りであり、各実施例の場合に
は摩擦係数が小さくて優れた潤滑性能を示すだけ
でなく、塗膜の耐水性も良好であつた。
This invention applies to rolling, forging or drawing of iron,
The present invention relates to a film-forming high-temperature lubricant composition used in hot working of various metals and alloys, such as extrusion of aluminum and copper, drawing of tungsten and molybdenum, etc. Conventionally, lubricant compositions of this type include lubricating oils, greases, or mixtures thereof with solid lubricants such as graphite powder or tungsten dioxide, or alkali metal sulfates, borates, potassium chloride, and sodium triacetate. An aqueous dispersion of a fine powder mixture consisting of graphite powder and an auxiliary agent added as necessary is known. However, the former is thermally unstable and decomposes during use, which has a negative impact on tools and workpieces, and the oil and oil decomposition products can seriously contaminate the working environment. Although the latter method does not have the same problems as the former method, it cannot be said that it exhibits satisfactory lubrication performance, especially in the production of seamless steel pipes. Therefore, the present inventors first developed a high-temperature lubricant mainly consisting of graphite powder and a plant-based polymer that can be dissolved or dispersed in water, as a solution to the problems with conventional lubricant compositions. (Japanese Patent Application No. 56-147297). Although this lubricant composition has achieved some success in that it does not contaminate the working environment and exhibits excellent lubrication performance at high temperatures, the water resistance of the lubricant film formed on metal surfaces has been limited. Unfortunately, for this reason, it is necessary to prevent water such as roll cooling water from leaking onto the lubricating coating at the work site, and if water leaks by mistake, the lubricating coating can easily wash off, peel off, or cause damage to the lubricating coating. There was a problem that the coating film thickness became uneven and its lubricating performance deteriorated, making it extremely difficult to use. The present invention was invented in view of this point of view, and aims to integrate graphite, resin, and water by using a plant-based polymer as a main ingredient, and improves the formability of a coating film.
A high-temperature lubricant that maintains workability, improves compatibility with the coated material by using synthetic polymers, and exhibits better performance, and forms a coating film with excellent water resistance. A composition is provided. That is, the present invention uses graphite powder of 50 to 94% by weight.
and 9 to 40% by weight of water-soluble or water-based plant-based polymer.
A film-forming high-temperature lubricant composition which further contains 1 to 20% by weight of a water-soluble or water-based plant-based polymer, and which is used as an aqueous lubricant dispersion by dispersing it in water. be. The graphite powder used in this invention may be natural or synthetic.
In addition, the particle size of this graphite powder is usually
Those with an average particle size of 100μ or less and a purity of at least 75% are used, of which an average particle size of 0.3 to 30
μ is preferable. Examples of water-soluble or water-dispersible plant polymers include starch and starch derivatives such as methyl starch, ethyl starch, acetyl starch, allyl starch, carboxymethyl starch, dialdehyde starch, oxidized starch, and modified starch, and amylose. and amylopectin and its derivatives such as amylose triacetate, dextrin and its derivatives, agar, cellulose derivatives such as cellulose ether, carboxymethyl cellulose, and cellulose xanthate, polysaccharides, polysaccharides such as gum arabic, guar gum, and gum substances, etc. can be mentioned. Starch systems consisting of starch, amylose, amylopectin, dextrin, and derivatives thereof are particularly preferred from the viewpoint of film-forming ability. These plant-based polymers are
They may be used alone or in combination of two or more. Furthermore, examples of water-soluble or water-dispersible synthetic polymers used in the present invention include liquid epoxy resins, liquid phenolic resins, liquid silicone resins, liquid alkyd resins, polyethylene glycol, polyethylene oxide, polypropylene oxide, and water-soluble modified polymers. Polyester resins, acrylic resins such as acrylic acid-butyl acrylate copolymers and acrylic acid-ethylene copolymers, styrene resins such as styrene-methyl methacrylate copolymers, and ethylene-vinyl acetate copolymers. Examples include vinyl acetate resin, liquid polyisobutylene, and the like. Among these, preferred are liquid epoxy resin, liquid phenol resin, polyethylene glycol, and ethylene glycol.
Examples include vinyl acetate copolymers, liquid alkyd resins, and modified polyester resins. Resins such as liquid epoxy resins, which cannot be dispersed in water alone, but which can be uniformly dispersed in a graphite suspension solution such as the present system, also fall within the category of water-dispersible synthetic polymers in the present invention. Furthermore, in the present invention, some plant-based polymers rot if left for a long period of time, so it is preferable to incorporate a preservative such as formaldehyde or ethyl paraoxybenzoate. The blending ratio of the film-forming high-temperature lubricant composition of the present invention is usually 50 to 90% by weight of graphite powder, 9 to 40% by weight of vegetable polymer, and 1 to 20% by weight of synthetic polymer, preferably , 60 to 85% by weight of graphite powder, 10 to 30% by weight of vegetable polymer, and 3 to 10% by weight of synthetic polymer. If the graphite powder content is less than 50% by weight, the desired lubrication performance cannot be obtained, and if it is more than 90% by weight, the film strength is insufficient and the desired lubrication performance cannot be obtained. Furthermore, if the amount of the plant-based polymer is less than 9% by weight, the uniformity of the film will be poor, and if it is more than 40% by weight, the strength of the film will be poor and the lubricating performance will deteriorate. Furthermore, if the synthetic polymer content is less than 1% by weight, the water resistance will be poor, and if it is more than 20% by weight, although the coating strength will be strong, the desired lubrication performance will not be obtained. The high temperature lubricant composition of the present invention is used as an aqueous lubricant dispersion by dispersing it in water, and the solid content concentration during use is usually 5 to 35% by weight, preferably 10 to 30% by weight. Adjust within the range of %. In addition, the solid content concentration may be adjusted, for example, once to a solid content concentration of 35 to 50% by weight, and then diluted at the time of use to a solid content concentration of 5 to 35% by weight. If the solid content concentration is too low, the drying time becomes long or the thickness of the formed coating film becomes thin, making it impossible to obtain good lubrication performance, and if the solid content concentration is too high, it becomes difficult to coat. The method for using the aqueous lubricant dispersion prepared in this way is to apply the aqueous lubricant dispersion to the surface of the metal to be hot-worked or to the surface of tools such as mandrels, dies, rolls, etc. by normal means. After drying this and forming a film on the surface of these metals and tools, hot working is performed. In addition, in the film-forming high-temperature lubricant composition of the present invention, conventionally known third components such as film stabilizers and rust inhibitors may be added to the composition in advance or when preparing the aqueous lubricant dispersion. It is also possible to add additives such as additives, antioxidants, surfactants, emulsifiers, extreme pressure agents, etc., and provide each characteristic with these additives. According to the present invention, by using a synthetic polymer in addition to a vegetable polymer, it is possible to enhance the lubricating performance of the lubricating film formed on the metal surface, and also to improve its water resistance. Extremely easy to handle. Hereinafter, the present invention will be specifically described based on Examples and Comparative Examples. Examples 1 to 8 and Comparative Examples 1 to 3 A lubricant composition was prepared by blending graphite powder, a vegetable polymer, and a synthetic polymer in the proportions shown in the table. A lubricant aqueous dispersion was prepared by dispersing the lubricant compositions of each example and each comparative example in water to a solid content concentration of 23% by weight, and this aqueous lubricant dispersion was heated to 200°C. It was spray coated onto a test piece (material: SKD-61) to form a lubricating film with a thickness of 60 μm on the surface of the test piece. This test piece was fixed in a friction and wear tester, and the temperature of the rolled rotating test piece was measured while being pressed against the test piece with lubricated surface pressure (sliding surface pressure) of 0.2 Kgf/mm 2 and 19.5 Kgf/ mm 2. Relative sliding speed at 1000℃
The friction coefficient under the condition of 1.5 m/s was determined. In addition, a method of spraying the lubricant aqueous dispersion prepared for the lubricant compositions of each Example and each Comparative Example onto a 50 mmφ x 150 mm SUS round bar heated to 200°C, and then pouring tap water after 10 seconds. The water resistance of the lubricating coating film formed was investigated. The results are shown in the table, and in each example, not only the coefficient of friction was small and the lubrication performance was excellent, but the water resistance of the coating film was also good.
【表】【table】
Claims (1)
性植物系高分子9〜40重量%とを主体とし、これ
にさらに水溶性又は水分散性合成高分子1〜20重
量%を含有し、水中に分散させて潤滑剤水分散液
として使用することを特徴とする被膜形成型高温
用潤滑剤組成物。 2 植物系高分子がデンプン、アミロース、アミ
ロペクチン、デキストリン及びこれらの誘導体並
びにグアーガムからなる一群から選択された1種
又は2種以上の組合せからなる特許請求の範囲第
1項記載の被膜形成型高温用潤滑剤組成物。 3 合成高分子がエポキシ樹脂、フエノール樹
脂、アルキド樹脂、ポリエチレングリコール、エ
チレン−酢酸ビニル共重合体及び変性ポリエステ
ル樹脂からなる一群から選択された1種又は2種
以上の組合せからなる特許請求の範囲第1項記載
の被膜形成型高温用潤滑剤組成物。[Scope of Claims] 1 Mainly composed of 50 to 90% by weight of graphite powder and 9 to 40% by weight of a water-soluble or water-dispersible vegetable polymer, and further 1 to 4% by weight of a water-soluble or water-dispersible synthetic polymer. A film-forming high-temperature lubricant composition containing 20% by weight and characterized in that it is used as an aqueous lubricant dispersion by dispersing it in water. 2. The film-forming high-temperature product according to claim 1, wherein the plant-based polymer is one or a combination of two or more selected from the group consisting of starch, amylose, amylopectin, dextrin, derivatives thereof, and guar gum. Lubricant composition. 3. Claim No. 3 in which the synthetic polymer is one or a combination of two or more selected from the group consisting of epoxy resin, phenolic resin, alkyd resin, polyethylene glycol, ethylene-vinyl acetate copolymer, and modified polyester resin. The film-forming high-temperature lubricant composition according to item 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11865682A JPS5911399A (en) | 1982-07-09 | 1982-07-09 | High temperature-use lubricant composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11865682A JPS5911399A (en) | 1982-07-09 | 1982-07-09 | High temperature-use lubricant composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5911399A JPS5911399A (en) | 1984-01-20 |
JPS6234360B2 true JPS6234360B2 (en) | 1987-07-27 |
Family
ID=14741960
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11865682A Granted JPS5911399A (en) | 1982-07-09 | 1982-07-09 | High temperature-use lubricant composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5911399A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6430441U (en) * | 1987-08-12 | 1989-02-23 | ||
JPH01147361A (en) * | 1987-12-03 | 1989-06-09 | Nkk Corp | Ultrasonic inspecting device |
GB2257712A (en) * | 1991-07-17 | 1993-01-20 | Hanano Corp | Lubricants for aluminium alloy forging |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0662980B2 (en) * | 1987-04-11 | 1994-08-17 | 日新製鋼株式会社 | Lubricating oil composition for stainless steel hot rolling |
JPH03203997A (en) * | 1989-12-28 | 1991-09-05 | Nippon Steel Chem Co Ltd | Lubricant for use at high temperature |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS51147448A (en) * | 1975-06-12 | 1976-12-17 | Nippon Kokuen Kogyo Kk | Method and device for lubricating roll in rolling mill |
-
1982
- 1982-07-09 JP JP11865682A patent/JPS5911399A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS51147448A (en) * | 1975-06-12 | 1976-12-17 | Nippon Kokuen Kogyo Kk | Method and device for lubricating roll in rolling mill |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6430441U (en) * | 1987-08-12 | 1989-02-23 | ||
JPH01147361A (en) * | 1987-12-03 | 1989-06-09 | Nkk Corp | Ultrasonic inspecting device |
GB2257712A (en) * | 1991-07-17 | 1993-01-20 | Hanano Corp | Lubricants for aluminium alloy forging |
Also Published As
Publication number | Publication date |
---|---|
JPS5911399A (en) | 1984-01-20 |
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