JPH03103498A - Lubricating oil composition - Google Patents
Lubricating oil compositionInfo
- Publication number
- JPH03103498A JPH03103498A JP24105989A JP24105989A JPH03103498A JP H03103498 A JPH03103498 A JP H03103498A JP 24105989 A JP24105989 A JP 24105989A JP 24105989 A JP24105989 A JP 24105989A JP H03103498 A JPH03103498 A JP H03103498A
- Authority
- JP
- Japan
- Prior art keywords
- lubricating oil
- lubricating
- fatty acid
- lanolin fatty
- acid value
- 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
- 239000010687 lubricating oil Substances 0.000 title claims abstract description 48
- 239000000203 mixture Substances 0.000 title claims abstract description 30
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 34
- 239000000194 fatty acid Substances 0.000 claims abstract description 34
- 229930195729 fatty acid Natural products 0.000 claims abstract description 34
- 235000019388 lanolin Nutrition 0.000 claims abstract description 26
- 239000004166 Lanolin Substances 0.000 claims abstract description 25
- 229940039717 lanolin Drugs 0.000 claims abstract description 25
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 23
- 239000002253 acid Substances 0.000 claims abstract description 22
- 239000003921 oil Substances 0.000 claims abstract description 21
- 239000000314 lubricant Substances 0.000 claims abstract description 15
- ZQKXQUJXLSSJCH-UHFFFAOYSA-N melamine cyanurate Chemical compound NC1=NC(N)=NC(N)=N1.O=C1NC(=O)NC(=O)N1 ZQKXQUJXLSSJCH-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000007787 solid Substances 0.000 claims abstract description 15
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000007788 liquid Substances 0.000 claims abstract description 12
- 230000001050 lubricating effect Effects 0.000 claims abstract description 6
- 239000002480 mineral oil Substances 0.000 claims abstract description 5
- 229920000642 polymer Polymers 0.000 claims abstract description 5
- 239000002199 base oil Substances 0.000 claims abstract description 4
- -1 fatty acid salt Chemical class 0.000 claims description 13
- 235000010446 mineral oil Nutrition 0.000 claims description 2
- 239000006185 dispersion Substances 0.000 abstract description 10
- 239000002270 dispersing agent Substances 0.000 abstract description 8
- 150000003839 salts Chemical class 0.000 abstract description 8
- 239000002245 particle Substances 0.000 abstract description 5
- 238000009826 distribution Methods 0.000 abstract description 4
- 238000002156 mixing Methods 0.000 abstract description 3
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 abstract description 3
- 238000009835 boiling Methods 0.000 abstract 1
- 235000019198 oils Nutrition 0.000 description 19
- 239000000047 product Substances 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- 238000000926 separation method Methods 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 4
- 125000002947 alkylene group Chemical group 0.000 description 4
- 239000010439 graphite Substances 0.000 description 4
- 229910002804 graphite Inorganic materials 0.000 description 4
- 238000005461 lubrication Methods 0.000 description 4
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 4
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000013049 sediment Substances 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 238000006297 dehydration reaction Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000002736 nonionic surfactant Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 229910052582 BN Inorganic materials 0.000 description 2
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000010775 animal oil Substances 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 239000010721 machine oil Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000010705 motor oil Substances 0.000 description 2
- 229920001195 polyisoprene Polymers 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- KZMAWJRXKGLWGS-UHFFFAOYSA-N 2-chloro-n-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]-n-(3-methoxypropyl)acetamide Chemical compound S1C(N(C(=O)CCl)CCCOC)=NC(C=2C=CC(OC)=CC=2)=C1 KZMAWJRXKGLWGS-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 239000010692 aromatic oil Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- YSXKPIUOCJLQIE-UHFFFAOYSA-N biperiden Chemical compound C1C(C=C2)CC2C1C(C=1C=CC=CC=1)(O)CCN1CCCCC1 YSXKPIUOCJLQIE-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000010727 cylinder oil Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 239000010696 ester oil Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000012208 gear oil Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000010720 hydraulic oil Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- JJTUDXZGHPGLLC-UHFFFAOYSA-N lactide Chemical compound CC1OC(=O)C(C)OC1=O JJTUDXZGHPGLLC-UHFFFAOYSA-N 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000011163 secondary particle Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000010723 turbine oil Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Landscapes
- Lubricants (AREA)
Abstract
Description
本発明は、新規な潤滑油組成物に関する。さらに詳しく
は潤滑性能と固体潤滑剤の分散安定性に優れた潤滑油組
成物に関するものである。The present invention relates to novel lubricating oil compositions. More specifically, the present invention relates to a lubricating oil composition having excellent lubrication performance and solid lubricant dispersion stability.
従来の潤滑油組成物としては、例えば合成油、鉱油、動
植物油などの、いわゆる潤滑油に各種の固体または液体
の添加剤を配合して潤滑油に、極圧性や耐摩擦性を付与
する努力がなされている。
例えば鍛造油、プレス油、引抜油、機械油等では黒色の
固体潤滑剤であるグラファイトや二硫化モリブデンの添
加が公知でありすでに実用化されている。また、モータ
ーオイル等では、例えば、特開昭55−23148号公
報に窒化ホウ素を、特開昭63−97693号公報にシ
リコーン樹脂をいずれも非イオン界面活性剤で分散した
ものが開示されている。さらに、非水系の固体潤滑剤用
分散剤としては、例えば、特開昭60−56760号公
報にボリオキシブロビレンアルキルエーテル、ボリオキ
シブロビレンアルキルフエニルエーテル等の非イオン界
面活性剤が開示されている。Conventional lubricating oil compositions include efforts to impart extreme pressure properties and friction resistance to lubricating oils by blending various solid or liquid additives with so-called lubricating oils, such as synthetic oils, mineral oils, animal and vegetable oils, etc. is being done. For example, the addition of black solid lubricants such as graphite and molybdenum disulfide to forging oil, press oil, drawing oil, machine oil, etc. is known and has already been put into practical use. Regarding motor oils, for example, JP-A No. 55-23148 discloses boron nitride, and JP-A No. 63-97693 discloses a silicone resin dispersed with a nonionic surfactant. Further, as dispersants for non-aqueous solid lubricants, for example, nonionic surfactants such as polyoxybrobylene alkyl ether and polyoxybrobylene alkyl phenyl ether are disclosed in JP-A-60-56760. ing.
しかしながら、このような従来の潤滑油組成物にあって
は、例えば、グラファイトや二硫化モリブデンの添加で
は黒色不透明なオイルである為、オイル劣化の判断が困
難であったり、使用時、加工製品への付着による黒色よ
ごれが発生し、これの改善が望まれている。また、テフ
ロン樹脂、窒化ホウ素、フッ化炭素、シリコーン{M脂
等が固体潤滑剤として使用される場合があり、これを潤
滑油に添加した場合、白色粉末である為、外観の改良が
図れ好ましいが、いずれも価格が高い為、限られた用途
でしか用いられない。さらに、前記した開示の非イオン
界面活性剤では、固体潤滑剤の分散安定性が充分でなく
、沈降層を形成するため、潤滑油として全く満足される
ものでなかった。一方、極圧性や耐摩擦性を向上させる
ための白色固体潤滑剤としては、最近メラミンシアヌレ
ートの粉末が有用であることが知られている。しかしな
がら、メラミンシアヌレートの粉末は有機の固体潤滑剤
で油に対して親和性が劣る為、潤滑油中での分散安定性
が極めて悪く、凝集する為、潤滑油に添加し分散調製し
ても、1日以内で沈降し、ハードケーキ化すると云う欠
点を有している。However, in such conventional lubricating oil compositions, for example, when graphite or molybdenum disulfide is added, the oil becomes black and opaque, making it difficult to judge whether the oil has deteriorated or causing damage to processed products during use. Black stains occur due to adhesion, and improvements to this problem are desired. In addition, Teflon resin, boron nitride, fluorocarbon, silicone (M fat, etc.) are sometimes used as solid lubricants, and when added to lubricating oil, they are white powders, which is preferable because they improve the appearance. However, due to their high prices, they are only used for limited purposes. Furthermore, the nonionic surfactants disclosed above do not have sufficient dispersion stability as solid lubricants and form a sedimentary layer, so they are not completely satisfactory as lubricating oils. On the other hand, it has recently been known that melamine cyanurate powder is useful as a white solid lubricant for improving extreme pressure properties and friction resistance. However, melamine cyanurate powder is an organic solid lubricant and has poor affinity for oil, so its dispersion stability in lubricating oil is extremely poor and it aggregates, so even if it is added to lubricating oil to prepare a dispersion. However, it has the disadvantage that it settles within one day and turns into a hard cake.
本発明者は上記問題を解決すべく鋭意研究を行った結果
、従来の技術では成し得なかった極めて長期安定性に優
れた潤滑油組成物を見出し、本発明を完成するに至った
。すなわち、合成油、又は鉱油より成る潤滑ベース油に
メラミンシアヌレートの固体潤滑剤と低酸価ラノリン脂
肪酸及び/又は低酸価ラノリン脂肪酸塩を必須成分とし
て含有することを特徴とする潤滑油組成物であり、また
、前記の潤滑油組或物に、分子ii5000〜1 00
000の液状イソプレン系ポリマーを添加することを特
徴とする潤滑油組成物である。
(手段を構成する要件)
本発明に使用する潤滑油としては、通常、油状潤滑油と
して用いられるものはいずれも使用でき、それらのうち
好ましいものとしては沸点が200℃以上(常圧下)の
潤滑油、たとえばナフテン系炭化水素油、パラフィン系
炭化水素油などの鉱油が使用できる。さらに、合成油で
はオレフインの重合より得られる合成炭化水素油、芳香
族類のアルキレーション反応より得られるアルキル化芳
香族油、さらに出発物質が炭素数8〜22の高級アルコ
ール、炭素数8〜20の高級脂肪酸又は炭素数6〜18
のアルキルもしくはアルケニル基を有するフェノールで
、これらとのアルキレンオキサイド付加物が使用できる
。前記のアルキレンオキサイドを付加したポリエーテル
油は通常公知の方法で合成できる。また、潤滑油として
用いる場合は、粘度が低く、親油性の強い潤滑性の高い
油が良好な為、アルキレンオキサイドの付加モル数は3
0モル以下が良い。さらにアルキレンオキサイドはブロ
ビレンオキサイド及び/又はプチレンオキサイドを付加
するのがよい。この付加方法についてはランダム、ブロ
ック付加、いずれの場合でも良いが、プチレンオキサイ
ドを単独で付加したものが特に良好である。
さらに、多価アルコールの脂肪酸エステル、高級アルコ
ールの脂肪酸エステル、低級アルコールの脂肪酸エステ
ル、アルカノールアミンの脂肪酸エステル等の合成エス
テル油及び動植物油が使用できる.
前記した潤滑油は、単独、又は、いずれかを配合して用
いる事ができ、通常室温において、5〜3000cpの
粘度を有するものが挙げられる。
次に:本発明に用いる固体潤滑剤は、メラミンとシアヌ
ル酸の付加反応物である有機系白色固体のメラミンシア
ヌレートを挙げることが出来る。
メラミンシアヌレートは日本で初めて見い出された有機
系白色固体の潤滑剤である。この物質の潤滑機構につい
ては、まだ十分に解明されていないが、二硫化モリブデ
ンやグラファイトと同じようなヘキ開性ラメラ構造に起
因していると考察され、潤滑油に添加すると、著しい潤
滑性能の向上が得られる。前記の固体潤滑剤は通常20
μ以下の粒子径であるが、平均粒子径0.02〜tOU
のもので、粒径分布のなるべ《均一なものを用いるのが
好ましい。
一方、本発明に用いるイソプレン系ポリマーとは、イソ
プレンを重合し、分子ffi5 0 0 0〜10oo
ooとした液状のポリイソプレンオリゴマ−を挙げるこ
とができる。
このポリイソプレンオリゴマーは、分子内に官能基を持
たないもの、又は水素添加処理品を用いるのが良い。さ
らにカルボキシル基及び水酸基の官能基を一部分子内に
持つもの、あるいは、これらから誘導されたエーテル化
合物、及びエステル化合物をも用いることが出来る。こ
れらは通常、公知の方法により製造することが出来る。
本発明に使用するイソプレン系ポリマーは分子量が50
00未満であると低酸価ラノリン脂肪酸及び/又は低酸
価ラノリン脂肪酸塩との併用によるメラミンシアヌレー
トの分散安定性で、向上が見られなくなる。又、分子1
1 00000をこえると粘度が高−《使用しにくいと
云う問題があり好ましくない。
本発明の非水系分散剤としては、低酸価ラノリン脂肪酸
と低酸価ラノリン脂肪酸塩が用いられる。前記の非水系
分散剤はウールグリースまたはラノリンを会化して分離
したラノリン脂肪酸より得る事が出来る。すなわち、第
1表に記載したような構成成分からなる混合物のラノリ
ン脂肪酸を高温脱水反応により酸価を低下せしめた低酸
価ラノリン脂肪酸ないしはその塩を用いる。
(以下余白)
その酸価および会化価は通常それぞれ130及至160
,160及至180である。上記組成からわかるように
ラノリン脂肪酸の主成分は炭素数が9〜32と非常に分
布の広い高級脂肪酸と炭素la12〜25のα−ヒドロ
キシ脂肪酸から成る。
したがって、ラノリン脂肪酸を無触媒ないしは任意のエ
ステル化触媒の存在下、好ましくは160〜220℃の
範囲内の温度で必要な酸価になるまで減圧加熱する事に
より低酸価ラノリン脂肪酸が得られる。また、ヒドロキ
シ脂肪酸を含有するかかるラノリン脂肪酸を減圧下で加
熱する事により、その2分子から2分子の水が脱水した
ラクチド、または分子内脱水によるラクトン等の環状エ
ステル、及び直鎖状モノー ボリー、エステルが生成す
ることは公知である。前記した低酸価ラノリン脂肪酸の
酸価は好ましくは1 2 5 mg−KOJI/gより
小さ<90より大きい値であり、さらに好ましくは11
5より小さ<100より大きい値である。酸価がこの範
囲外にあると分散能が劣るため、酸価を制御する事が重
要である。
すなわちラノリン脂肪酸の高温脱水状態により、ヒドロ
キシ脂肪酸に関わるヒドロキシル基と、分布の非常に広
い分岐アルキル基から成る脂肪酸のカルボキシル基との
エステルから成る特殊な構造であり、潤滑油の分散媒と
メラミンシアメレートに対する親和性の向上効果が表わ
れ、好結果が得られるものと考えられる。また、あらか
じめラノリン脂肪酸を潤滑油で溶解して、上記エステル
化反応を実施し得る。
又、かかる低酸価ラノリン脂肪酸の塩も有効である。塩
型としては例えばナトリウム、カリウム、リチウム等の
アルカリ金属、カルシウム、バリウム、マグネシウム、
鉛及び亜鉛等のアルカリ土類金属が挙げられる。さらに
アンモニア又はアミン等の塩であってもよい。
アミンの例としてはアルキルアミン、エチレンジアミン
、ジエチレントリアミン、トリエチレンテトラミン等の
ポリアミン、モルホリン、ビペリジン、アルカノールア
ミン等を挙げることができる。
かかる中和反応は低酸価ラノリン脂肪酸と酸価に見合っ
た塩基を、200℃までの温度で加熱撹拌する事により
得られる。この場合、反応は有機溶媒、例えば石油留分
等の潤滑油に溶解して行うのが好ましい。
さらに、未反応の金属の酸化物、水酸化物は濾過等によ
り除去するのが良い.耐摩耗性、摩t?R緩和性より塩
はアルカリ土類金属がより好ましい。
これらのラノリン脂肪酸及びその塩は2 fffi以上
の混合物として使用してちよい。
潤滑油組成物のメラミンシアヌレートの濃度は分散系が
生成されるいずれの濃度でもよいが、通常0.05〜4
0!!11%がほとんどであり、0.05重量%より少
ない場合は満足し得る潤滑性能が得られず、逆に40重
量%より多い場合は経済上好ましくない。又、分散剤は
潤滑油組成物全系に対し0.1〜20重量%、好ましく
は0.5〜10重量%添加するのが望ましい。
潤滑油組成物の製造方法としては、例えば,分散剤を溶
解した潤滑油に所定量のメラミンシアヌレートを添加し
、ついで、メラミンシアヌレートの二次粒子を崩すこと
ができる程度のせん断力をもった分散機、すなわち具体
的には3本ロール,コロイドミル、ホモジナイザー、ボ
ールミル、ラインミキサーなどにより、充分撹拌混合す
る。
本発明の潤滑油組成物には必要により、酸化防止剤、防
錆剤、腐食防止剤、消泡剤、耐荷重添加剤、抗乳化剤、
清浄分散剤、本発明以外の公知の分散剤を併用すること
もできる。As a result of intensive research aimed at solving the above problems, the present inventors discovered a lubricating oil composition with extremely excellent long-term stability, which could not be achieved using conventional techniques, and completed the present invention. That is, a lubricating oil composition characterized by containing a solid lubricant of melamine cyanurate and a low acid value lanolin fatty acid and/or a low acid value lanolin fatty acid salt as essential components in a lubricating base oil consisting of synthetic oil or mineral oil. and the lubricating oil composition has a molecule ii of 5000 to 100
This is a lubricating oil composition characterized by adding 000 liquid isoprene-based polymer. (Requirements constituting the means) As the lubricating oil used in the present invention, any lubricating oil that is normally used as an oily lubricating oil can be used. Oils such as naphthenic hydrocarbon oils, mineral oils such as paraffinic hydrocarbon oils can be used. Furthermore, synthetic oils include synthetic hydrocarbon oils obtained from polymerization of olefins, alkylated aromatic oils obtained from alkylation reactions of aromatics, and higher alcohols with 8 to 22 carbon atoms as starting materials, and higher alcohols with 8 to 22 carbon atoms as starting materials. Higher fatty acid or carbon number 6-18
phenol having an alkyl or alkenyl group, and alkylene oxide adducts with these can be used. The polyether oil to which alkylene oxide has been added can be synthesized by a commonly known method. In addition, when used as a lubricating oil, an oil with low viscosity, strong lipophilicity, and high lubricating properties is good, so the number of moles of alkylene oxide added is 3.
It is preferably 0 mole or less. Furthermore, it is preferable to add brobylene oxide and/or butylene oxide to the alkylene oxide. This addition method may be random or block addition, but adding butylene oxide alone is particularly preferred. Furthermore, synthetic ester oils such as fatty acid esters of polyhydric alcohols, fatty acid esters of higher alcohols, fatty acid esters of lower alcohols, fatty acid esters of alkanolamines, and animal and vegetable oils can be used. The above lubricating oils can be used alone or in combination, and include those having a viscosity of 5 to 3000 cp at room temperature. Next: The solid lubricant used in the present invention includes melamine cyanurate, which is an organic white solid and is an addition reaction product of melamine and cyanuric acid. Melamine cyanurate is an organic white solid lubricant that was first discovered in Japan. The lubrication mechanism of this substance has not yet been fully elucidated, but it is thought to be due to the cleavage lamellar structure similar to molybdenum disulfide and graphite, and when added to lubricating oil, it significantly improves lubrication performance. Improvement can be obtained. The solid lubricant mentioned above is usually 20
The particle size is less than μ, but the average particle size is 0.02 to tOU.
It is preferable to use one with a uniform particle size distribution. On the other hand, the isoprene-based polymer used in the present invention is obtained by polymerizing isoprene and has a molecular ffi of 5000 to 10oo.
Examples include liquid polyisoprene oligomers designated as OO. It is preferable to use a polyisoprene oligomer that does not have a functional group in its molecule or a hydrogenated product. Furthermore, compounds having some carboxyl and hydroxyl functional groups in their molecules, or ether compounds and ester compounds derived from these can also be used. These can usually be manufactured by known methods. The isoprene polymer used in the present invention has a molecular weight of 50
If it is less than 00, no improvement will be seen in the dispersion stability of melamine cyanurate when used in combination with a low acid value lanolin fatty acid and/or a low acid value lanolin fatty acid salt. Also, molecule 1
If it exceeds 100,000, the viscosity is high and it is difficult to use, which is not preferable. As the non-aqueous dispersant of the present invention, low acid value lanolin fatty acids and low acid value lanolin fatty acid salts are used. The above-mentioned non-aqueous dispersant can be obtained from wool grease or lanolin fatty acid separated by agglomeration of lanolin. That is, a low-acid-value lanolin fatty acid or a salt thereof is used, which is obtained by lowering the acid value of a lanolin fatty acid mixture consisting of the constituent components shown in Table 1 through a high-temperature dehydration reaction. (Left below) Its acid value and chemical value are usually 130 to 160, respectively.
, 160 to 180. As can be seen from the above composition, the main components of lanolin fatty acids are higher fatty acids having a very wide distribution of carbon numbers of 9 to 32, and α-hydroxy fatty acids having 12 to 25 carbon atoms. Therefore, low acid value lanolin fatty acids can be obtained by heating lanolin fatty acids without a catalyst or in the presence of any esterification catalyst, preferably at a temperature within the range of 160 to 220° C., under reduced pressure until the required acid value is reached. In addition, by heating such lanolin fatty acid containing hydroxy fatty acid under reduced pressure, two molecules of water are dehydrated from the lanolin fatty acid, resulting in lactide, or cyclic ester such as lactone due to intramolecular dehydration, and linear monoboly, It is known that esters are produced. The acid value of the low acid value lanolin fatty acid described above is preferably less than 125 mg-KOJI/g<90, more preferably 11
The value is smaller than 5 and larger than 100. If the acid value is outside this range, the dispersibility will be poor, so it is important to control the acid value. In other words, due to the high-temperature dehydration state of lanolin fatty acids, it has a special structure consisting of esters of hydroxyl groups related to hydroxy fatty acids and carboxyl groups of fatty acids consisting of branched alkyl groups with a very wide distribution, and is compatible with lubricating oil dispersion media and melamine resin. It is thought that the effect of improving the affinity for amerate appears and good results are obtained. Alternatively, the above esterification reaction can be carried out by dissolving the lanolin fatty acid in lubricating oil in advance. Salts of such low acid value lanolin fatty acids are also effective. Examples of salts include alkali metals such as sodium, potassium, and lithium, calcium, barium, magnesium,
Examples include alkaline earth metals such as lead and zinc. Furthermore, salts such as ammonia or amines may be used. Examples of amines include alkylamines, polyamines such as ethylenediamine, diethylenetriamine, and triethylenetetramine, morpholine, biperidine, and alkanolamines. Such a neutralization reaction can be obtained by heating and stirring a low acid value lanolin fatty acid and a base commensurate with the acid value at a temperature of up to 200°C. In this case, the reaction is preferably carried out in an organic solvent, for example in a lubricating oil such as a petroleum fraction. Furthermore, it is recommended to remove unreacted metal oxides and hydroxides by filtration, etc. Abrasion resistance, abrasion t? In terms of R relaxation, the salt is preferably an alkaline earth metal. These lanolin fatty acids and their salts may be used as a mixture of 2 fffi or more. The concentration of melamine cyanurate in the lubricating oil composition may be any concentration that produces a dispersion, but is usually 0.05 to 4.
0! ! Most of the content is 11%, and if it is less than 0.05% by weight, satisfactory lubrication performance cannot be obtained, whereas if it is more than 40% by weight, it is economically unfavorable. Further, it is desirable to add the dispersant in an amount of 0.1 to 20% by weight, preferably 0.5 to 10% by weight, based on the entire lubricating oil composition. As a method for producing a lubricating oil composition, for example, a predetermined amount of melamine cyanurate is added to a lubricating oil in which a dispersant is dissolved, and then a shearing force is applied to an extent that can break up the secondary particles of melamine cyanurate. The mixture is sufficiently stirred and mixed using a dispersing machine such as a three-roll mill, colloid mill, homogenizer, ball mill, line mixer, etc. The lubricating oil composition of the present invention may optionally contain antioxidants, rust inhibitors, corrosion inhibitors, antifoaming agents, load-bearing additives, demulsifiers,
A detergent dispersant and a known dispersant other than those of the present invention can also be used in combination.
このようにして得られた潤滑油組成物は、メラミンシア
ヌレートの分散安定性にすぐれ、たとえば6ケ月以上と
いった長期間にわたって放置しても、またたとえば80
℃といった高温下においても安定性が格投に優れている
。また本発明の潤滑油組成物は良好な極圧性と低い摩擦
係数を有し,一般機械への潤滑油、たとえば冷凍油、各
種エンジン油、スピンドル油、ダイナモ油、マシン油、
タービン油、ギャー油、シリンダー油、その他の各種作
動油などに配合して苛酷な条件下においても焼付きを防
止し、摺動面の摩耗量の減少に大きな効果を発揮する。
さらには金属加工油、繊維プラスチック処理用の潤滑油
などとしても有効である。これらの、加工処理の工程で
本発明の潤滑油組成物を使用すると、グラファイトや、
二硫化モリブデンの様な黒色液でない為、製品への付着
または機械や作業場への付着による黒色汚染が無く、格
段に優れた製品のクリーン化が図り得る。
以下、この発明の実施例を記載してより具体的に説明す
るが、本発明はこれらの実施例に限定されるものではな
い。The lubricating oil composition thus obtained has excellent dispersion stability of melamine cyanurate, and even when left for a long period of time, for example, 6 months or more,
It has excellent stability even at high temperatures such as ℃. Furthermore, the lubricating oil composition of the present invention has good extreme pressure properties and a low coefficient of friction, and can be used as a lubricating oil for general machinery, such as refrigeration oil, various engine oils, spindle oil, dynamo oil, machine oil,
When mixed with turbine oil, gear oil, cylinder oil, and various other hydraulic oils, it prevents seizure even under severe conditions and is highly effective in reducing the amount of wear on sliding surfaces. Furthermore, it is effective as a metal processing oil, a lubricating oil for processing fiber plastics, etc. When the lubricating oil composition of the present invention is used in these processing steps, graphite,
Since it is not a black liquid like molybdenum disulfide, there is no black contamination caused by adhesion to products or machines or workplaces, making it possible to make products much cleaner. EXAMPLES Hereinafter, the present invention will be described in more detail by describing examples, but the present invention is not limited to these examples.
各種の潤滑油に、分敗剤を溶解したのち、メラミンシア
ヌレートを添加し、1mmφガラスビーズを用いたビー
ズミルで充分混合して均一に分敗し、第2表に示す潤滑
油組成物を得た。
ここで調製した潤滑油組成物について,200ml2の
メスシリンダーに移し、25℃の恒温槽に180日間保
存し、シリングー内の液を観察し、液分離又はハードな
沈降層の様姿を下記評価基準にて分散経口安定性を判定
した。さらに、別に上記潤滑油組成物の摺動性評価とし
て、ファレックス試験機による摩擦係数と限界荷重量を
測定し、これらの結果を第3表に示した。
0:液分離や沈降物が認められない
○:わずかな液分離があるが、沈降物は認められない
Δ:少し液分離あり、ソフトな沈降物が少し認められる
×:液分離多く、ハードな沈降物が多く認められる
(以下余白)
上記の試験結果より、本発明の潤滑油組成物は長期間の
安定性に優れていることと、摩擦係数、及び耐荷重性に
優れている結果が得られた。さらに、潤滑油による付着
汚染も少なく、良好な潤滑油が得られる事がわかった。After dissolving a separating agent in various lubricating oils, melamine cyanurate was added and thoroughly mixed in a bead mill using 1 mm diameter glass beads to uniformly separate the lubricating oil compositions shown in Table 2. Ta. The lubricating oil composition prepared here was transferred to a 200 ml graduated cylinder, stored in a constant temperature bath at 25°C for 180 days, and the liquid in the cylinder was observed, and the appearance of liquid separation or hard sedimentation was evaluated using the following evaluation criteria. Dispersion oral stability was determined. Furthermore, as a separate evaluation of the sliding properties of the lubricating oil composition, the friction coefficient and limit load were measured using a Farex tester, and the results are shown in Table 3. 0: No liquid separation or sediment observed ○: Slight liquid separation, but no sediment observed Δ: Slight liquid separation, some soft sediment observed ×: Much liquid separation, hard Many sediments are observed (blank below). The above test results show that the lubricating oil composition of the present invention has excellent long-term stability, friction coefficient, and load resistance. It was done. Furthermore, it was found that a good lubricating oil could be obtained with less adhesion and contamination caused by the lubricating oil.
メラミンシアヌレートを固体潤滑剤とする製品は粉末品
、及び粘調なグリース状品であり、非水系溶媒の分欣液
は凝集性が強い為、製造困難であった。しかし、本発明
の潤滑油組成物の完成で、低粘度で安定性の高い分散液
の製品が得られる事となり、ハンドリング性の良好な、
潤滑性に優れ、新規な潤滑油を安価に使用しつる事から
、潤滑油素材の提供を通じ、金属、機械工業の産業発展
に広く寄与しつるものである。Products using melamine cyanurate as a solid lubricant are powder products and viscous grease-like products, and the separation solution of non-aqueous solvents has strong cohesive properties, making it difficult to manufacture. However, by completing the lubricating oil composition of the present invention, a dispersion product with low viscosity and high stability can be obtained, and it has good handling properties.
Because it has excellent lubricity and allows the use of new lubricating oils at low cost, it has widely contributed to industrial development in the metal and machinery industries by providing lubricating oil materials.
Claims (1)
シアヌレートの固体潤滑剤と低酸価ラノリン脂肪酸及び
/又は低酸価ラノリン脂肪酸塩を必須成分として含有す
ることを特徴とする潤滑油組成物。 2、請求項1記載の潤滑油組成物に、分子量5000〜
100000の液状イソプレン系ポリマーを添加するこ
とを特徴とする潤滑油組成物。[Claims] 1. A lubricating base oil made of synthetic oil or mineral oil contains a solid lubricant of melamine cyanurate and a low acid value lanolin fatty acid and/or a low acid value lanolin fatty acid salt as essential components. A lubricating oil composition. 2. The lubricating oil composition according to claim 1 has a molecular weight of 5000 to
A lubricating oil composition characterized in that 100,000% of a liquid isoprene-based polymer is added.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24105989A JPH03103498A (en) | 1989-09-18 | 1989-09-18 | Lubricating oil composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24105989A JPH03103498A (en) | 1989-09-18 | 1989-09-18 | Lubricating oil composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03103498A true JPH03103498A (en) | 1991-04-30 |
Family
ID=17068697
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP24105989A Pending JPH03103498A (en) | 1989-09-18 | 1989-09-18 | Lubricating oil composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03103498A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000328086A (en) * | 1999-05-25 | 2000-11-28 | Nippon Koyu:Kk | Sticky lubricating composition |
CN1079111C (en) * | 1999-01-25 | 2002-02-13 | 李政兆 | Additive composition of lubricating oil |
-
1989
- 1989-09-18 JP JP24105989A patent/JPH03103498A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1079111C (en) * | 1999-01-25 | 2002-02-13 | 李政兆 | Additive composition of lubricating oil |
JP2000328086A (en) * | 1999-05-25 | 2000-11-28 | Nippon Koyu:Kk | Sticky lubricating composition |
JP4693946B2 (en) * | 1999-05-25 | 2011-06-01 | 株式会社日本礦油 | Adhesive lubricating composition |
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