JPS6261637B2 - - Google Patents
Info
- Publication number
- JPS6261637B2 JPS6261637B2 JP56040452A JP4045281A JPS6261637B2 JP S6261637 B2 JPS6261637 B2 JP S6261637B2 JP 56040452 A JP56040452 A JP 56040452A JP 4045281 A JP4045281 A JP 4045281A JP S6261637 B2 JPS6261637 B2 JP S6261637B2
- Authority
- JP
- Japan
- Prior art keywords
- present
- lubricating oil
- power transmission
- propylene
- traction
- 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
- 239000010687 lubricating oil Substances 0.000 claims description 22
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 21
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 15
- 230000005540 biological transmission Effects 0.000 claims description 12
- 150000004996 alkyl benzenes Chemical class 0.000 claims description 9
- 238000009835 boiling Methods 0.000 claims description 6
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 5
- 239000008096 xylene Substances 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 3
- 229920001155 polypropylene Polymers 0.000 claims description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 10
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 8
- 239000003921 oil Substances 0.000 description 8
- 230000003647 oxidation Effects 0.000 description 7
- 238000007254 oxidation reaction Methods 0.000 description 7
- 239000003054 catalyst Substances 0.000 description 5
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 5
- 238000005096 rolling process Methods 0.000 description 5
- JRZJOMJEPLMPRA-UHFFFAOYSA-N 1-nonene Chemical compound CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 238000005804 alkylation reaction Methods 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 150000001721 carbon Chemical group 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- RQFVHGAXCJVPBZ-UHFFFAOYSA-N propylene pentamer Chemical compound CC=C.CC=C.CC=C.CC=C.CC=C RQFVHGAXCJVPBZ-UHFFFAOYSA-N 0.000 description 3
- WBULCZWMWLOUQW-UHFFFAOYSA-N 10-methylundecylbenzene Chemical compound CC(C)CCCCCCCCCC1=CC=CC=C1 WBULCZWMWLOUQW-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- ORILYTVJVMAKLC-UHFFFAOYSA-N adamantane Chemical compound C1C(C2)CC3CC1CC2C3 ORILYTVJVMAKLC-UHFFFAOYSA-N 0.000 description 2
- 230000029936 alkylation Effects 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- -1 hydrogenation 1 Chemical compound 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000003449 preventive effect Effects 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 238000013112 stability test Methods 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- FUZBYNWONHYNOB-UHFFFAOYSA-N 1-cyclohexylethylcyclohexane Chemical compound C1CCCCC1C(C)C1CCCCC1 FUZBYNWONHYNOB-UHFFFAOYSA-N 0.000 description 1
- ROFWOEQFASWFTK-UHFFFAOYSA-N 1-cyclohexylpropylcyclohexane Chemical compound C1CCCCC1C(CC)C1CCCCC1 ROFWOEQFASWFTK-UHFFFAOYSA-N 0.000 description 1
- RXEXJOJJFMWBFB-UHFFFAOYSA-N 7-methyloctylbenzene Chemical compound CC(C)CCCCCCC1=CC=CC=C1 RXEXJOJJFMWBFB-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 1
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000003254 anti-foaming effect Effects 0.000 description 1
- 238000007630 basic procedure Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
Landscapes
- Lubricants (AREA)
Description
本発明は動力伝達装置用潤滑油に関し、特にト
ラクシヨンドライブ用として適切な動力伝達装置
用潤滑油に関する。
動力の伝達、変速には従来より歯車や油圧装置
が用いられているが、トラクシヨンドライブ(転
がり摩擦駆動装置)といわれる回転剛体間の点接
触あるいは線接触の駆動方式も知られ、歯車のか
み合い等を伴わず、運転中の振動も少なく、また
動力伝達効率の高い事から一部産業機械にも実用
化され始めている。
この場合、接触部分に介在する油には機能上か
ら最も適した潤滑油を選定しなければならない。
すなわち、接触部分に介在する油は、高圧下で可
逆的にガラス転移を生じて粘度上昇する事により
回転接触面における動力伝達効果が大きく、接触
面を離れるとただちに流動状態に戻る性質を有
し、かつ金属間の直接接触を防ぎ、焼付き摩耗、
疲労損傷を防止し、また一般潤滑油と同様な防
錆、冷却等の重要な作用をも有しなければならな
い。
本発明はこのような動力伝達装置用潤滑油、特
にトラクシヨンドライブに供されるのに適切な潤
滑油に関する。
動力伝達用の摩擦又はトラクシヨンドライブ装
置は多くの先行する技術文献に記載されており、
例えばアメリカ特許第3394603号、同第3411369
号、ジヤーナル・オブ・ケミカル・アンド・エン
ジニアリングデータ第5巻第4号、499〜507頁、
ヒユーコ等のローリング接触現象に関するシンポ
ジウム議事録157〜185頁ニルセビア出版社(アム
ステルダム)1962年に詳しい。
またトラクシヨンドライブ用潤滑油としては鉱
油(特公昭39−24635号)、ポリメチルメタクリレ
ート(特公昭48−31828号)、ピバリン酸モノエス
テル(特公昭49−11309号)、ハロゲン化アルキル
ナフタレン(特公昭49−16900号)、アダマンタン
類(特公昭48−42067号、同48−42068号)、ポリ
オレフイン(特開昭46−4766号、同47−2229
号)、アルキルナフタレン(アメリカ特許第
2549377号)など多数が提案されているが、水素
化された環を有するナフテン系油に関する提案も
多い。
提案されたナフテン系油としてはジシクロヘキ
シルエタン(特公昭48−29715号)、ジシクロヘキ
シルプロパン(特公昭53−36105号)、水素化縮合
環化合物(アメリカ特許第3411369号)、1以上の
飽和炭素環を有するナフテン(アメリカ特許第
3440894号)、2以上の飽和炭素環を有するナフテ
ン(アメリカ特許第3925217号)、ナフテンとパラ
フインの混合油(アメリカ特許第3595796号、同
第3595797号)がある。またキシレンおよび/ま
たはトルエンとスチレンのアルキル化反応生成物
を水素化して得られるもの(主として水素化1,
1−ジアリルエタン系化合物)等についても知ら
れている。
前述のアメリカ特許第3440894号および同第
3925217号の各明細書に記載の技術は広範なナフ
テン系化合物を含み、多数のナフテンを例示して
いるが、その多くは水素化された環を有する化合
物である。またトラクシヨン特性の優れたものに
は、40℃における粘度が20cst以上の比較的高い
ものが多い。一方、実使用に当たつては、トラク
シヨンドライブの効率がころがり面以外の作動部
における粘性抵抗によつて低下する為、またころ
がり表面の冷却性を高める為にもトラクシヨンド
ライブに供される潤滑油は出来る限り低粘度油で
ある事が望ましい。
そこで、本発明の目的は、粘性抵抗、冷却性の
点を満足し、かつトラクシヨン特性が優れている
ばかりでなく、酸化安定性、耐腐蝕性等の点にお
いても優れた性能を有し、しかも工業的見地から
すれば極めて安価な原料を用いる事ができる動力
伝達装置用潤滑油を提供する事にある。
本発明者らは特定のアルキルベンゼンがその分
子構造から本発明の目的に対し特異的に有効であ
る事を見出し、本発明をなすに到つた。
本発明に係る動力伝達装置用潤滑油はプロピレ
ン重合物とベンゼン又はトルエン又はキシレンと
の反応によつて得られる沸点範囲(常圧換算)
250〜450℃のアルキルベンゼンを主成分とする潤
滑油である。ここで、沸点範囲(常圧換算)が
250℃未満の場合、本発明に係る潤滑油の引火性
に、および450℃を越える場合はその粘性特性お
よび冷却性能に各々問題を生じるため、本発明に
おいては上記本発明の沸点範囲外のアルキルベン
ゼンは除外される。
上記本発明のアルキルベンゼンの代表的具体例
としては、アルキル基成分がプロピレントリマー
型のイソノニルベンゼンおよびプロピレンテトラ
マー型のイソドデシルベンゼンおよびプロピレン
ペンタマー型のイソペンタデシルベンゼン並びに
これらの製造時に副生する重質アルキルベンゼン
などがある。これらのうち、本発明において特に
望ましいものはプロピレンテトラマー型のイソド
デシルベンゼンである。ただし、ここでいうプロ
ピレントリマーとは、いわゆるプロピレンの三量
体を工業的に製造する際に得られるもので、炭素
原子数範囲としてはC9を主成分とする7〜11の
分布を持ち、またプロピレンテトラマーは同様に
炭素原子数範囲が10〜15、さらにプロピレンペン
タマーは同様に炭素原子数範囲が13〜18の分布を
もつものである。
これら本発明のアルキルベンゼンは、例えばプ
ロピレンをリン酸触媒を用いて温度100〜300℃、
圧力10〜60Kg/cm2にて重合させたプロピレントリ
マー(三量体)およびプロピレンテトラマー(四
量体)およびプロピレンペンタマー(五量体)あ
るいはこれらの混合物を弗化水素、硫酸、塩化ア
ルミニウム等フリーデルクラフツ型触媒を用いて
ベンゼン又はトルエン又はキシレンと反応する事
により得られる。そして塩化アルミニウムを触媒
とした場合、反応温度は20〜150℃の範囲が採用
できるが、40〜80℃の範囲が有利である。また反
応圧力は1〜10Kg/cm2Gが有利である。なお、重
質アルキルベンゼンはアルキレーシヨンの際に副
生して得られる。本発明において用いられるベン
ゼン又はトルエン又はキシレンは極めて入手しや
すく且つ安価であるが、収率の点などからベンゼ
ンを用いる事が望ましい。
本発明に係る動力伝達装置用潤滑油に少量の鉱
油、他のナフテン系油等を含有せしめることは差
し支えなく、また本発明に係る潤滑油は酸化安定
性、熱安定性、耐食性、防錆性、せん断安定性、
耐摩耗性等について十分な性能を有するが、これ
らの性能を向上させる目的で酸化防止剤、腐食防
止剤、防錆剤、消泡剤等の添加剤を含有せしめる
こともできる。また、本発明のアルキルベンゼン
を製造する過程に生成する副生物が少量存在する
事も何ら差支えない。
トラクシヨン係数の測定については、一般にト
ラクシヨンドライブ装置を用いて行われるが、本
発明においては曽田式円筒式摩擦試験機を用い
た。トラクシヨン(転がり摩擦)は、中心におか
れた円筒とその外側に配置された3ケの円筒との
3ケ所の接触部で行われ、接触部には同一の垂直
荷重が作用する。この時の面圧は、平均ヘルツ圧
力にして0.575〜1.157GPaである。他の条件は下
記第1表のとおりである。
The present invention relates to a lubricating oil for a power transmission device, and particularly to a lubricating oil for a power transmission device suitable for use in a traction drive. Gears and hydraulic devices have traditionally been used to transmit power and change speeds, but a drive system called traction drive (rolling friction drive device) that uses point or line contact between rotating rigid bodies is also known. It is beginning to be put into practical use in some industrial machinery because it has no vibrations during operation, and has high power transmission efficiency. In this case, the most suitable lubricating oil must be selected from the functional point of view as the oil present in the contact area.
In other words, the oil present in the contact area undergoes a reversible glass transition under high pressure and increases in viscosity, which has a large power transmission effect on the rotating contact surface, and has the property of returning to a fluid state immediately after leaving the contact surface. , and prevents direct contact between metals, preventing seizure wear,
It must prevent fatigue damage and also have important functions such as rust prevention and cooling similar to general lubricating oils. The present invention relates to a lubricating oil for such power transmission devices, and particularly to a lubricating oil suitable for use in traction drives. Friction or traction drive devices for power transmission have been described in many prior technical documents;
For example, US Patent No. 3394603, US Patent No. 3411369
No., Journal of Chemical and Engineering Data, Vol. 5, No. 4, pp. 499-507,
Proceedings of a symposium on rolling contact phenomena by Huyuko et al., pp. 157-185, Nilsevier Publishers (Amsterdam), 1962. Lubricating oils for traction drives include mineral oil (Japanese Patent Publication No. 39-24635), polymethyl methacrylate (Japanese Patent Publication No. 48-31828), pivalic acid monoester (Japanese Patent Publication No. 49-11309), and halogenated alkylnaphthalene (Japanese Patent Publication No. 49-11309). Publication No. 49-16900), adamantane (Japanese Patent Publication No. 48-42067, 48-42068), polyolefins (Japanese Patent Publication No. 4766-1976, 47-2229)
), alkylnaphthalene (U.S. Patent No.
2549377), but there are also many proposals regarding naphthenic oils having hydrogenated rings. The proposed naphthenic oils include dicyclohexylethane (Japanese Patent Publication No. 48-29715), dicyclohexylpropane (Japanese Patent Publication No. 53-36105), hydrogenated condensed ring compounds (US Patent No. 3411369), and one or more saturated carbon rings. naphthenes (U.S. patent no.
3440894), naphthene having two or more saturated carbon rings (US Patent No. 3925217), and mixed oils of naphthenes and paraffins (US Patent Nos. 3595796 and 3595797). Also, those obtained by hydrogenating alkylation reaction products of xylene and/or toluene and styrene (mainly hydrogenation 1,
1-diallylethane type compounds) and the like are also known. U.S. Pat. No. 3,440,894 and U.S. Pat.
The technology described in each specification of No. 3925217 includes a wide range of naphthenic compounds and exemplifies a large number of naphthenes, many of which are compounds with hydrogenated rings. Furthermore, many of those with excellent traction properties have a relatively high viscosity of 20 cst or more at 40°C. On the other hand, in actual use, the efficiency of the traction drive decreases due to viscous resistance in the operating parts other than the rolling surface, and it is also used in the traction drive to improve the cooling performance of the rolling surface. It is desirable that the lubricating oil be as low in viscosity as possible. Therefore, the object of the present invention is to not only satisfy the viscous resistance and cooling properties and have excellent traction properties, but also to have excellent performance in terms of oxidation stability, corrosion resistance, etc. From an industrial standpoint, the object of the present invention is to provide a lubricating oil for power transmission devices that can use extremely inexpensive raw materials. The present inventors have discovered that a specific alkylbenzene is specifically effective for the purpose of the present invention due to its molecular structure, and has accomplished the present invention. The lubricating oil for power transmission devices according to the present invention has a boiling point range (converted to normal pressure) obtained by reacting a propylene polymer with benzene, toluene, or xylene.
It is a lubricating oil whose main component is alkylbenzene with a temperature of 250 to 450℃. Here, the boiling point range (converted to normal pressure) is
If the temperature is less than 250°C, there will be problems with the flammability of the lubricating oil according to the present invention, and if it exceeds 450°C, there will be problems with its viscosity characteristics and cooling performance. are excluded. Typical specific examples of the alkylbenzenes of the present invention include isononylbenzene in which the alkyl group component is of the propylene trimer type, isododecylbenzene of the propylene tetramer type, isopentadecylbenzene of the propylene pentamer type, and by-produced during their production. Heavy alkylbenzenes, etc. Among these, propylene tetramer type isododecylbenzene is particularly desirable in the present invention. However, the propylene trimer here is obtained when so-called propylene trimer is produced industrially, and has a carbon atom number range of 7 to 11, with C9 as the main component. Similarly, propylene tetramer has a carbon atom number range of 10 to 15, and propylene pentamer has a carbon atom number range of 13 to 18. These alkylbenzenes of the present invention can be produced using, for example, propylene at a temperature of 100 to 300°C using a phosphoric acid catalyst.
Propylene trimer (trimer), propylene tetramer (tetramer), propylene pentamer (pentamer) or a mixture thereof polymerized at a pressure of 10 to 60 Kg/cm 2 is treated with hydrogen fluoride, sulfuric acid, aluminum chloride, etc. It is obtained by reacting with benzene, toluene, or xylene using a Friedel-Crafts type catalyst. When aluminum chloride is used as a catalyst, the reaction temperature can range from 20 to 150°C, but is preferably from 40 to 80°C. Moreover, the reaction pressure is advantageously 1 to 10 kg/cm 2 G. Note that heavy alkylbenzene is obtained as a by-product during alkylation. Although benzene, toluene, or xylene used in the present invention is extremely easily available and inexpensive, it is desirable to use benzene from the viewpoint of yield. The lubricating oil for power transmission devices according to the present invention may contain a small amount of mineral oil, other naphthenic oil, etc., and the lubricating oil according to the present invention has oxidation stability, thermal stability, corrosion resistance, and rust prevention properties. , shear stability,
Although it has sufficient performance in terms of wear resistance, etc., additives such as antioxidants, corrosion inhibitors, rust preventives, antifoaming agents, etc. can be contained in order to improve these performances. Further, there is no problem in the presence of a small amount of by-products generated during the process of producing the alkylbenzene of the present invention. The traction coefficient is generally measured using a traction drive device, but in the present invention, a Soda type cylindrical friction tester was used. Traction (rolling friction) occurs at three contact points between the central cylinder and three cylinders placed outside, and the same vertical load acts on the contact points. The surface pressure at this time is 0.575 to 1.157 GPa in terms of average Hertzian pressure. Other conditions are as shown in Table 1 below.
【表】
実験の操作手順としては、まず回転速度を内・
外円筒共一定にし、荷重を負荷した後、外筒の回
転数のみ増加する事によつてすべり率を上昇せし
め、すべり率に対する摩擦トルク、あるいはトラ
クシヨン係数の変化を連続的に求めた。摩擦トル
クは中央の無心支持軸のねじれモーメントを抵抗
線ひずみ計で直接測定する事によつて行つた。
この条件において測定されるトラクシヨン係数
は、すべり率の増加に伴つてまず直線的に立ち上
がり、その後極大を描いて低下する傾向を示す。
この場合、特に実用面において重要な領域は、油
膜のせん断による発生熱が大きくない初期の直線
領域にあり、特にこの領域のトラクシヨン係数を
以下対象とする。
一例として平均ヘルツ圧力1.157GPa、回転速
度4.19m/S、すべり速度0.022m/Sにて測定し
たトラクシヨン係数は下記第2表の通りである
が、本発明による潤滑油はトラクシヨン係数0.07
以上と、これらの炭化水素に比べて優れている事
が明らかとなつた。[Table] The operating procedure for the experiment is to first adjust the rotation speed to
After applying a load while keeping the outer cylinder constant, the slip rate was increased by increasing only the rotational speed of the outer cylinder, and changes in friction torque or traction coefficient relative to the slip rate were continuously determined. Friction torque was measured by directly measuring the torsional moment of the central free support shaft using a resistance wire strain gauge. The traction coefficient measured under these conditions shows a tendency to first rise linearly as the slip rate increases, then reach a maximum and then decline.
In this case, the particularly important region from a practical standpoint is the initial linear region where the heat generated by shearing the oil film is not large, and the traction coefficient in this region will be of particular interest below. As an example, the traction coefficient measured at an average Hertz pressure of 1.157 GPa, a rotational speed of 4.19 m/S, and a sliding speed of 0.022 m/S is shown in Table 2 below, and the lubricating oil according to the present invention has a traction coefficient of 0.07.
From the above, it has become clear that it is superior to these hydrocarbons.
【表】
トラクシヨンドライブ用潤滑油に要求される性
能としては、上記のトラクシヨン特性以外に、一
般の潤滑油に要求される酸化安定性、粘度指数、
耐腐食性、耐摩耗性、サビ止め性、ゴム潤滑性、
泡立ち防止性などが挙げられ、それぞれの用途に
応じて適当な添加剤を配合する事が必要となる。
ここで本発明に係る潤滑油に、これらの添加剤、
例えば酸化防止剤として2,6−ジターシヤリー
ブチルパラクレゾールなどのアルキルフエノー
ル、ジアルキルジチオリン酸亜鉛などのいおう、
りん化合物を、防錆剤としてアミン、エステル、
金属塩を、粘度指数向上剤としてポリメタアクリ
レート類を、消泡剤としてシリコーン系重合物等
を各々1種または2種以上添加する事が可能であ
る。
以下実施例を挙げて本発明を例証するが、本発
明の実施態様はこれらに限定されない。
実施例
プロピレンを固形リン酸触媒を用いて温度190
℃、圧力35Kg/cm2の条件で重合し、プロピレンテ
トラマー(四量体)とする。このプロピレンテト
ラマーは、副生ポリマーを含むので、蒸留により
沸点範囲170〜230℃の留分を採取した。このプロ
ピレンテトラマーの代表的な組成は例えば
Analytical chemistry Vol.35,12(1963)2219
にもとずいた分析法によれば、二重結合の位置に
より三置換体45%、四置換体37%、二置換体が16
%、一置換体が残余であつた。次いで上記沸点範
囲のプロピレンテトラマーを塩化アルミニウムを
触媒として、ベンゼン1部に塩化アルミニウム
0.01部を加え、70℃に加温し、ベンゼンと反応さ
せ、いわゆるアルキレーシヨンしてドデシルベン
ゼンを得た。このドデシルベンゼンには副生アル
キルベンゼンを含んでいるので蒸留し、沸点範囲
170〜185℃(圧力13mmHg)の留分を採取した。
上記ドデシルベンゼンのトラクシヨン係数は0.07
であり、その一般性状は下記第3表の通りであつ
た。[Table] In addition to the above-mentioned traction properties, the performance required for lubricating oils for traction drives includes oxidation stability, viscosity index, and viscosity index required for general lubricating oils.
Corrosion resistance, wear resistance, rust prevention, rubber lubricity,
Examples include anti-foaming properties, and it is necessary to mix appropriate additives depending on each application.
Here, these additives,
For example, as antioxidants, alkylphenols such as 2,6-ditertiarybutyl para-cresol, zinc dialkyldithiophosphate, etc.
Phosphorus compounds are used as rust preventive agents such as amines, esters,
It is possible to add one or more metal salts, polymethacrylates as a viscosity index improver, and silicone polymers as an antifoaming agent. The present invention will be illustrated below with reference to Examples, but the embodiments of the present invention are not limited thereto. Example Propylene was heated to 190°C using a solid phosphoric acid catalyst.
Polymerize under the conditions of ℃ and 35 kg/cm 2 pressure to form propylene tetramer (tetramer). Since this propylene tetramer contains by-product polymers, a fraction with a boiling point range of 170 to 230°C was collected by distillation. The typical composition of this propylene tetramer is, for example:
Analytical chemistry Vol.35, 12 (1963) 2219
According to an analytical method based on
%, monosubstituted product remained. Next, propylene tetramer having the above boiling point range was mixed with aluminum chloride in 1 part of benzene using aluminum chloride as a catalyst.
0.01 part was added, heated to 70°C, reacted with benzene, and subjected to so-called alkylation to obtain dodecylbenzene. This dodecylbenzene contains by-product alkylbenzene, so it is distilled to reduce the boiling point range.
A fraction between 170 and 185°C (pressure: 13 mmHg) was collected.
The traction coefficient of the above dodecylbenzene is 0.07
The general properties were as shown in Table 3 below.
【表】
上記のドデシルベンゼンについてフエノール系
および亜鉛系酸化防止剤をそれぞれ0.5wt%添加
し、酸化試験をJIS−K−2514−1980(潤滑油酸
化安定度試験法)3.2項(内燃機関用潤滑油酸化
安定度試験方法)に記載された基本手順に従つて
行つた。その結果を下記第5表、第6表および第
7表に示す。下記の第5〜7表は下記の市販ナフ
テン系鉱油と本発明による潤滑油との酸化試験結
果を比較したものである。[Table] To the above dodecylbenzene, 0.5wt% each of phenolic and zinc antioxidants were added and the oxidation test was carried out in JIS-K-2514-1980 (Lubricating oil oxidation stability test method) Section 3.2 (Internal combustion engine lubrication The test was carried out according to the basic procedure described in the Oil Oxidation Stability Test Method. The results are shown in Tables 5, 6 and 7 below. Tables 5 to 7 below compare the oxidation test results of the following commercially available naphthenic mineral oils and the lubricating oil according to the present invention.
【表】 なお、試験条件は下記第4表の通りである。【table】 The test conditions are shown in Table 4 below.
【表】【table】
【表】【table】
【表】【table】
【表】
上記の第5〜7表に示した結果から明らかなよ
うに本発明による潤滑油は極めて優れた安定性を
有する事が判る。[Table] As is clear from the results shown in Tables 5 to 7 above, it can be seen that the lubricating oil according to the present invention has extremely excellent stability.
Claims (1)
はキシレンとの反応によつて得られる沸点範囲
(常圧換算)250〜450℃のアルキルベンゼンから
なる動力伝達装置用潤滑油。 2 動力伝達装置がトラクシヨンドライブである
ことを特徴とする特許請求の範囲第1項記載の動
力伝達装置用潤滑油。[Scope of Claims] 1. A lubricating oil for a power transmission device comprising an alkylbenzene having a boiling point range (converted to normal pressure) of 250 to 450°C obtained by the reaction of a propylene polymer and benzene, toluene, or xylene. 2. The lubricating oil for a power transmission device according to claim 1, wherein the power transmission device is a traction drive.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4045281A JPS57155295A (en) | 1981-03-23 | 1981-03-23 | Lubricating oil for power transmitting apparatus |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4045281A JPS57155295A (en) | 1981-03-23 | 1981-03-23 | Lubricating oil for power transmitting apparatus |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57155295A JPS57155295A (en) | 1982-09-25 |
JPS6261637B2 true JPS6261637B2 (en) | 1987-12-22 |
Family
ID=12581022
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4045281A Granted JPS57155295A (en) | 1981-03-23 | 1981-03-23 | Lubricating oil for power transmitting apparatus |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57155295A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7402715B2 (en) | 2001-08-08 | 2008-07-22 | Idemitsu Kosan Co., Ltd. | Fluids for traction drive |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1357406A (en) * | 1970-09-23 | 1974-06-19 | Monsanto Co | Force transmission using synthetic fluids |
US4005159A (en) * | 1973-10-04 | 1977-01-25 | The Lubrizol Corporation | Hydroxy containing phosphonates |
JPS5336105A (en) * | 1976-09-16 | 1978-04-04 | Fujitsu Ltd | Synchronous circuit connecting system |
JPS5575495A (en) * | 1978-12-05 | 1980-06-06 | Nippon Petrochem Co Ltd | Power transmitting fluid |
-
1981
- 1981-03-23 JP JP4045281A patent/JPS57155295A/en active Granted
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1357406A (en) * | 1970-09-23 | 1974-06-19 | Monsanto Co | Force transmission using synthetic fluids |
US4005159A (en) * | 1973-10-04 | 1977-01-25 | The Lubrizol Corporation | Hydroxy containing phosphonates |
JPS5336105A (en) * | 1976-09-16 | 1978-04-04 | Fujitsu Ltd | Synchronous circuit connecting system |
JPS5575495A (en) * | 1978-12-05 | 1980-06-06 | Nippon Petrochem Co Ltd | Power transmitting fluid |
Also Published As
Publication number | Publication date |
---|---|
JPS57155295A (en) | 1982-09-25 |
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