JPH0587117B2 - - Google Patents

Info

Publication number
JPH0587117B2
JPH0587117B2 JP30922387A JP30922387A JPH0587117B2 JP H0587117 B2 JPH0587117 B2 JP H0587117B2 JP 30922387 A JP30922387 A JP 30922387A JP 30922387 A JP30922387 A JP 30922387A JP H0587117 B2 JPH0587117 B2 JP H0587117B2
Authority
JP
Japan
Prior art keywords
weight
component
present
traction
traction drive
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP30922387A
Other languages
Japanese (ja)
Other versions
JPH01149898A (en
Inventor
Juji Ikemoto
Hiroshi Kinoshita
Giichi Murai
Kanji Mochizuki
Atsushi Kaiya
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eneos Corp
Original Assignee
Nippon Oil Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nippon Oil Corp filed Critical Nippon Oil Corp
Priority to JP30922387A priority Critical patent/JPH01149898A/en
Priority to GB8828450A priority patent/GB2224287B/en
Priority to DE3841609A priority patent/DE3841609A1/en
Publication of JPH01149898A publication Critical patent/JPH01149898A/en
Publication of JPH0587117B2 publication Critical patent/JPH0587117B2/ja
Granted legal-status Critical Current

Links

Description

【発明の詳现な説明】[Detailed description of the invention]

産業䞊の利甚分野 本発明はトラクシペンドラむブ甚流䜓組成物に
関し、詳しくはトラクシペン係数および高枩特性
に優れたトラクシペンドラむブ甚流䜓組成物に関
する。 埓来の技術 けん匕駆動装眮、䟋えばボヌルコヌン型、コ
ヌンリング型、ホむヌルデむスク型、チ゚ヌ
ンシヌブ型、トロむダル型、遊星ロヌラ型など
のけん匕駆動装眮の動力䌝達郚においおは、ころ
がり接觊面においお最滑油の油膜が硬化するこず
により生じるころがり摩擊を利甚しお動力が䌝達
されるため、そこに甚いられる最滑剀、すなわち
トラクシペンドラむブ甚流䜓は優れた動力䌝達胜
力、すなわち高いけん匕係数を有するこずが芁求
される。 たた同時に、トラクシペンドラむブ甚流䜓はト
ラクシペンドラむブ装眮の高速皌動時には極めお
高枩条件䞋にさらされるため、高枩条件䞋でも摩
擊面で油膜圢が可胜ずなるためには高枩特性、す
なわち、高枩での蒞発損倱量が少なく、か぀高枩
でもある皋床以䞊の粘床を有するこずが芁求され
る。 埓来より、トラクシペンドラむブ甚流䜓に぀い
いおは、䟋えば特公昭46−338号、同46−339号、
同47−7664号、同48−29715号、同48−42067号、
同48−42068号、同53.−36105号、同58−12319
号、同58−27838号、同60−1353号、同60−1354
号、同60−19951号、同60−43391号、同60−
43392号をはじめ、その他倚くの特蚱や文献など
で皮々の化合物が提案されおいる。 発明が解決しようずする問題点 しかしながら、䞊蚘に瀺した公知のトラクシペ
ンドラむブ甚流䜓は、原料入手が困難、補造方法
が耇雑、トラクシペン係数が実甚に適さないなど
の理由によ぀お実甚化されたものが少なく、わず
かに特公昭53−36105号および同58−12319号で提
案された−ゞシクロヘキシル−−メチル
ペンタンが実甚性のあるものずしお、そのたた流
䜓ずしお、たたはこれに増ちよう剀を配合しおグ
リヌスずしお䜿甚されおいる皋床である。 しかしながら、この−ゞシクロヘキシル
−−メチルペンタンは優れたトラクシペン係数
を有するものの、高枩条件䞋では蒞発損倱量が倚
く、たた粘床も䜎くな぀おしたうずいう欠点があ
぀た。 本発明者らは䞊述したような埓来公知のトラク
シペンドラむブ甚流䜓が有する欠点を克服すべく
研究を重ねた結果、特定された構造、性質を有す
る化合物を特定比率で混合した組成物がトラクシ
ペンドラむブ甚流䜓ずしお各皮性胜に優れるこず
を芋い出し、本発明を完成するに至぀た。 本発明は、トラクシペン係数が高く、か぀高枩
特性に優れる、すなわち高枩条件䞋での蒞発損倱
量が少なく、粘床特性に優れたトラクシペンドラ
むブ甚流䜓組成物を提䟛するこずを目的ずする。 問題点を解決するための手段 本発明は、 () (A) スクワラン、および (B) 炭玠数〜12のオレフむンの少なくずも皮
を単独重合たたは共重合するこずにより埗られ
る、40℃での動粘床が〜40cStか぀平均分子量
が100〜500のポリオレフむン油からなる矀より遞
ばれる皮たたは皮以䞊の鎖状炭化氎玠化合
物、20〜80重量、 ならびに () 䞀般匏
INDUSTRIAL APPLICATION FIELD The present invention relates to a fluid composition for traction drives, and more particularly to a fluid composition for traction drives that has excellent traction coefficients and high-temperature properties. BACKGROUND TECHNOLOGY In the power transmission section of a traction drive device such as a ball & cone type, cone & ring type, wheel & disc type, chain & sheave type, toroidal type, or planetary roller type, the rolling contact surface Since power is transmitted using the rolling friction created by the hardening of the lubricating oil film, the lubricant used there, that is, the traction drive fluid, must have excellent power transmission ability, that is, a high traction coefficient. is required. At the same time, the traction drive fluid is exposed to extremely high temperature conditions when the traction drive device operates at high speeds, so in order to form an oil film on the friction surface even under high temperature conditions, it is necessary to have high temperature characteristics. It is required to have a small amount of evaporation loss and a certain level of viscosity even at high temperatures. Conventionally, regarding traction drive fluid, for example, Japanese Patent Publication No. 46-338, No. 46-339,
No. 47-7664, No. 48-29715, No. 48-42067,
No. 48-42068, No. 53.-36105, No. 58-12319
No. 58-27838, No. 60-1353, No. 60-1354
No. 60-19951, No. 60-43391, No. 60-
Various compounds have been proposed in Patent No. 43392 and many other patents and documents. Problems to be Solved by the Invention However, the known traction drive fluids listed above have not been put into practical use due to reasons such as difficulty in obtaining raw materials, complicated manufacturing methods, and unsuitable traction coefficients for practical use. 2,4-dicyclohexyl-2-methylpentane, which was proposed in Japanese Patent Publications No. 53-36105 and No. 58-12319, is considered to be practical, and may be used as a fluid as it is or be expanded to this. It is only used as a grease by blending it with an agent. However, although this 2,4-dicyclohexyl-2-methylpentane has an excellent traction coefficient, it has the drawbacks of high evaporation loss and low viscosity under high temperature conditions. The present inventors have conducted extensive research to overcome the drawbacks of the conventionally known traction drive fluids as described above, and as a result, a composition containing compounds having specified structures and properties in a specific ratio has been developed. The present inventors have discovered that this fluid has excellent performance as a drive fluid, and have completed the present invention. An object of the present invention is to provide a fluid composition for a traction drive that has a high traction coefficient and excellent high-temperature properties, that is, has low evaporation loss under high-temperature conditions and excellent viscosity properties. Means for Solving the Problems The present invention provides a polymeric polymer at 40°C obtained by homopolymerizing or copolymerizing at least one of () (A) squalane and (B) an olefin having 3 to 12 carbon atoms. one or more chain hydrocarbon compounds selected from the group consisting of polyolefin oils having a kinematic viscosity of 2 to 40 cSt and an average molecular weight of 100 to 500, 20 to 80% by weight, and () General formula

【化】 匏䞭、はたたはの敎数を瀺し、R1およ
びR2はR1のずきR2CH3、R1CH3のずき
R2ずなる基をそれぞれ瀺す。で衚わされる
ポリシクロヘキシルアルカン、80〜20重量、 を混合しおなるこずを特城ずするトラクシペンド
ラむブ甚流䜓組成物を提䟛するものである。 以䞋、本発明の内容をより詳现に説明する。 本発明でいう成分ずは、 (A) スクワラン、および (B) 炭玠数〜12のオレフむンの少なくずも皮
を単独重合たたは共重合するこずにより埗られ
る、40℃での動粘床が〜40cStか぀平均分子量
が100〜500のポリオレフむン油からなる矀より遞
ばれる皮たたは皮以䞊の鎖状炭化氎玠化合物
である。 ここでいう(A)スクワランずは、10
151923−ヘキサメチルテトラコサン化孊匏
C30H62ずいう飜和鎖状炭化氎玠を䞻成分ずす
る無色透明、無味無臭の液䜓であり、工業的には
䟋えば鮫肝油などの魚油やオリヌブ油などの怍物
油から分離粟補しお埗られるスクワレンをさらに
氎玠化觊媒を甚いお高枩、高圧䞋で氎玠添加する
するこずにより、たたむ゜フむトヌル合成の原料
ずしお入手可胜なゲラニルアセトンこのものは
む゜プレンから合成されるず倩然ガスの分解に
よるアセチレン補造の際に副生する―ブタ
ゞむンの反応生成物を氎玠添加分解するこずによ
り埗られる。 たたここでいう(B)ポリオレフむン油ずは、炭玠
数〜12のオレフむン、具䜓的には䟋えばプロピ
レン、ブテン、ヘキセン、オクテン、デセン、ド
デセンなど、の少なくずも皮を単独重合たたは
共重合するこずにより埗られる、動粘床〜
40cSt40℃か぀平均分子量100〜500のポリオ
レフむン油のこずであり、具䜓的には䞊蚘の性状
を有するポリプロピレン、ポリブテン、ポリむ゜
ブチレン、ポリヘキセン、ポリオクテン、ポリデ
セン、ポリドデセンおよびこれらの混合物などが
挙げられる。ポリオレフむン油ずしおは䞊蚘の性
状に加えお、さらに−30℃以䞋、奜たしくは−40
℃以䞋の流動点を有するものが望たしい。 このポリオレフむン油の補造法は圓業者に呚知
のものであり、塩化アルミニりム、塩化アルミニ
りム−臭化アルミニりム系、塩化アルミニりム−
゚ステル系、臭化アルミニりム、臭化アルミニり
ム−臭化氎玠系、塩化マグネシりム、北化ホり
玠、北化ホり玠−アルコヌル系などのいわゆるフ
リヌデル・クラフツ觊媒たたはそれらの錯化合物
等を甚いたカチオン重合、熱やパヌオキサむドに
よるラゞカル重合あるいはチヌグラヌ系觊媒によ
る重合等によ぀おなされ、いかなる方法によ぀お
も䞊蚘の性状を満たすものならば本発明に䜿甚す
るこずができる。さらに本発明においおは䞊蚘の
ポリオレフむン油が含有する二重結合を既知の方
法、䟋えばニツケルたたはニツケルモリブデン酞
塩觊媒などを甚いお氎玠添加した氎添ポリオレフ
むン油も䜿甚できる。 さらに本発明の成分ずしおは、䞊蚘の(A)
スクワランおよび(B)ポリオレフむン油を任意の割
合で混合しお混合物も䜿甚可胜である。 䞀方、本発明でいう成分ずは、䞀般匏
[Formula, n represents an integer of 0 or 1, R 1 and R 2 are R 2 = CH 3 when R 1 = H, and R 2 = CH 3 when R 1 = CH 3
Each group represents a group in which R 2 =H. The present invention provides a fluid composition for traction drive, characterized in that it is made by mixing 80 to 20% by weight of polycyclohexyl alkane represented by: Hereinafter, the content of the present invention will be explained in more detail. In the present invention, the component () is obtained by homopolymerizing or copolymerizing at least one of (A) squalane and (B) an olefin having 3 to 12 carbon atoms, and has a kinematic viscosity of 2 at 40°C. One or more chain hydrocarbon compounds selected from the group consisting of polyolefin oils having a weight of ~40 cSt and an average molecular weight of 100 to 500. (A) Squalane here means 2, 6, 10,
15,19,23-hexamethyltetracosane (chemical formula
It is a colorless, transparent, tasteless and odorless liquid whose main component is a saturated chain hydrocarbon called C 30 H 62 ).Industrially, squalene is obtained by separating and refining fish oil such as shark liver oil or vegetable oil such as olive oil. Furthermore, acetylene can be produced by hydrogenation under high temperature and high pressure using a hydrogenation catalyst, and by decomposition of natural gas and geranylacetone (which is synthesized from isoprene), which is available as a raw material for isophytol synthesis. It is obtained by hydrogenolyzing the reaction product of 1,3-butadiyne, which is produced as a by-product. In addition, (B) polyolefin oil here refers to a homopolymerization or copolymerization of at least one olefin having 3 to 12 carbon atoms, specifically, for example, propylene, butene, hexene, octene, decene, dodecene, etc. Kinematic viscosity 2~
It refers to polyolefin oil with an average molecular weight of 40cSt (@40℃) and 100 to 500, and specifically includes polypropylene, polybutene, polyisobutylene, polyhexene, polyoctene, polydecene, polydodecene, and mixtures thereof having the above properties. It will be done. In addition to the above-mentioned properties, the polyolefin oil should also have a temperature below -30°C, preferably -40°C.
It is desirable that the pour point is below ℃. The manufacturing method of this polyolefin oil is well known to those skilled in the art, and includes aluminum chloride, aluminum chloride-aluminum bromide system, aluminum chloride-aluminum bromide system,
Cationic polymerization using so-called Friedel-Crafts catalysts such as ester, aluminum bromide, aluminum bromide-hydrogen bromide, magnesium chloride, boron fluoride, boron fluoride-alcohol, or their complex compounds, etc. Any method can be used in the present invention as long as it satisfies the above properties, such as by radical polymerization using a peroxide or a Ziegler catalyst. Furthermore, in the present invention, a hydrogenated polyolefin oil obtained by hydrogenating the double bonds contained in the above-mentioned polyolefin oil using a known method such as a nickel or nickel molybdate catalyst can also be used. Furthermore, as the component () of the present invention, the above (A)
It is also possible to use a mixture of squalane and (B) polyolefin oil in any proportion. On the other hand, the component () as used in the present invention refers to the general formula

【化】 で衚わされるポリシクロヘキシルアルカンであ
る。䞊匏䞭、はたたはの敎数を瀺し、R1
およびR2はR1のずきR2CH3、R1CH3の
ずきR2ずなる基をそれぞれ瀺しおいる。 この成分であるポシクロリヘキシルアル
カンは、䟋えばα−メチルスチレンを重合する
か、たたはポリ−α−メチルスチレンを熱分解す
るこずによ぀おトリプニルアルカンたたはテト
ラプニルアルカンを埗、次いでこれらを栞氎玠
添加するこずにより補造できる。具䜓的には䟋え
ば、α−メチルスチレンの重合は酞性癜土、掻性
癜土、シリカ−アルミナ、モンモリナむト型粘
床、シリカゲル等の固䜓酞觊媒を䜿甚し、これに
氎、二䟡アルコヌル、゚ヌテルなどの含酞玠化合
物を反応調節剀ずしお䜵甚しお加熱䞋、α−メチ
ルスチレンを反応させるこずにより容易に行え
る。たた栞氎玠添加反応は、䟋えばニツケル、ニ
ツケル−ケむ゜り土、ラネ−ニツケル、癜金、癜
金−アルミナ、ロゞりム、ロゞりム−アルミナな
どの栞氎玠添加觊媒を甚いお、䞊蚘のポリプニ
ルアルカンを高枩、高圧䞋で氎玠ず接觊させるこ
ずにより容易に行える。 䞊述の方法で埗られるポリシクロヘキシルアル
カンは、条件によ぀おは本発明の成分以倖
の構造をも぀ものゞシクロヘキシルアルカン、
ペンタシクロヘキシルアルカン、環状化合物な
ども副生物ずしお混合しおいる堎合もあるの
で、必芁に応じお蒞留などの分離操䜜により、目
的ずする化合物を取り出すこずができる。 本発明のトラクシペンドラむブ甚流䜓組成物に
おいお、成分ず成分の混合比率は、
成分20〜80重量、奜たしくは30〜70重量
に察しお、成分80〜20重量、奜たしく
は70〜30重量である。成分の混合比率が
䞊蚘範囲に満たない堎合は組成物の粘床が高くな
りすぎ、特に成分のみでは垞枩で半固䜓状
であり、実甚に䟛するこずはできない。䞀方
成分の混合比率が䞊蚘範囲を超える堎合は
組成物の高枩特性およびトラクシペン係数が䜎く
なるため、それぞれ奜たしくない。 本発明においおは前蚘成分ず成分
を特定比率で混合するこずにより各皮性胜に優れ
たトラクシペンドラむブ甚流䜓が埗られるが、そ
の䜎枩特性および高枩特性を損なわない範囲で
−ゞシクロヘキシル−−メチルペンタン
を含有するこずもできる。この−ゞシクロ
ヘキシル−−メチルペンタンの含有量は任意で
あるが、通垞、成分であるポリシクロヘキ
シルアルカン100重量郚に察しお100重量郚以䞋、
奜たしくは50重量郚以䞋である。この−ゞ
シクロヘキシル−−メチルペンタンを䜵甚する
堎合は、本発明の成分ず成分を混合
しお本発明に係わるトラクシペンドラむブ甚流䜓
組成物を埗、その埌に−ゞシクロヘキシル
−−メチルペンタンを混合しおもよい。たた前
述したずおり成分をα−メチルスチレンの
重合によ぀お補造する堎合には、反応条件によ぀
お成分の他に−ゞシクロヘキシル−
−メチルペンタンも副生するため、副生した
−ゞシクロヘキシル−−メチルペンタン
を分離陀去するこずなく成分ずの混合物の
圢で成分ず混合しおもよい。 たた前述したずおり、成分をα−メチル
スチレンの重合によ぀お補造する堎合には、反応
条件によ぀お成分の他に環状化合物α−
メチルスチレンの環状二量䜓、環状䞉量䜓および
環状四量䜓の栞氎玠添加物も副生するこずがあ
るが、これらの環状化合物も本発明の効果を損な
わない範囲で本発明のトラクシペンドラむブ甚流
䜓組成物に含たれおいおもよい。 たた本発明のトラクシペンドラむブ甚流䜓組成
物に、必芁に応じお通垞䜿甚される各皮の最滑油
添加剀を添加するこずができる。具䜓的には䟋え
ば、−ゞ−−ブチル−−クレゟヌルな
どのヒンダヌドプノヌル、プニル−α−ナフ
チルアミンなどの芳銙族アミン、ゞアルキルゞチ
オりん酞亜鉛などの有機金属化合物、スルフむ
ド、ゞスルフむドなどのむオり化合物に代衚され
る酞化防止剀、カルボン酞、スルホン酞、りん酞
塩、アミン、アルコヌル、゚ステルなどのさび止
め剀、有機むオり化合物、有機ハロゲン化合物、
ゞアルキルゞチオりん酞亜鉛、ゞアルキルゞチオ
りん酞モリブデン、ゞアルキルゞチオカルバミン
酞モリブデンなどの有機金属塩、りん酞゚ステル
などに代衚される極圧剀、ポリメタクリレヌト、
ポリむ゜ブチレンなどに代衚される粘床指数向䞊
剀、シリコヌン油などの消泡剀などを添加でき
る。これら公知の最滑油添加剀の添加量も任意で
あるが、通垞、合蚈添加量が組成物党量基準で含
有量が20重量以䞋、奜たしくは10重量以䞋ず
なるように添加するのが望たしい。 さらにグリヌス甚ずしお公知の有機系たたは無
機系の増ちよう剀、具䜓的には䟋えば、リチりム
石けん、ナトリりム石けん、カルシりム石けんな
どの石けん系増ちよう剀、リチりムコンプレツク
ス石けん、カルシりムコンプレツクス石けん、ア
ルミニりムコンプレツクス石けんなどのコンプレ
ツクス石けん系増ちよう剀、有機シロキサン、テ
レフタラメヌト、ポリりレア、有機凊理粘土、シ
リカ゚アロゲルなど非石けん系増ちよう剀を本発
明のトラクシペンドラむブ甚流䜓組成物に混合
し、トラクシペングリヌスずしお䜿甚するこずも
できる。トラクシペングリヌスずしお䜿甚する際
の増ちよう剀の混合量は任意であるが、通垞グリ
ヌス組成物党量基準で増ちよう剀の含有量が〜
30重量、奜たしくは〜20重量ずなるように
混合するのが奜たしい。 発明の実斜䟋 以䞋、本発明の内容を実斜䟋および比范䟋によ
りさらに具䜓的に説明する。 実斜䟋〜および比范䟋〜 衚に瀺す組成により本発明に係わるトラクシ
ペンドラむブ甚流䜓組成物実斜䟋〜を埗
た。なお、衚に瀺す各成分は以䞋の性状を有す
るものである。 成分 スクワラン 鮫肝油から埗られるスクワランをさらに氎玠添
加しお埗られる10151923−ヘキサ
メチルテトラコサンを䞻成分ずするもの。粘床
18.9cSt40℃、流動点−65℃以䞋、匕火点230
℃、平均分子量423。 ポリブテン ナフサ分解により生成するブタン−ブテン留分
を䜎重合させお埗られるむ゜ブチレン−−ブテ
ン共重合䜓。動粘床2.7cSt40℃、流動点−70
℃以䞋、匕火点87℃、平均分子量220。 ポリブテン ナフサ分解により生成するブタン−ブテン留分
を䜎重合させお埗られるむ゜ブチレン−−ブテ
ン共重合䜓。動粘床7.5cSt40℃、流動点−
67.5℃、匕火点115℃、平均分子量280。 −デセンオリゎマヌ −デセンの䜎重合により埗られる分枝鎖状炭
化氎玠化合物。動粘床17.5cSt40℃、流動点
−73℃、匕火点216℃、平均分子量353。 成分 ポリシクロヘキシルアルカン 掻性癜土を觊媒ずしおα―メチルスチレンを重
合した生成物をニツケル系觊媒で栞氎玠添加した
埌、蒞留によ぀お埗られる沞点415〜430℃垞圧
換算の留分、垞枩20℃で半固䜓状であり、
It is a polycyclohexyl alkane represented by In the above formula, n represents an integer of 0 or 1, and R 1
and R 2 represent a group in which R 2 =CH 3 when R 1 =H, and R 2 =H when R 1 =CH 3 . This component (), polycyclohexylalkane, is produced by, for example, polymerizing α-methylstyrene or thermally decomposing poly-α-methylstyrene to obtain triphenylalkane or tetraphenylalkane, and then These can be produced by nuclear hydrogenation. Specifically, for example, in the polymerization of α-methylstyrene, a solid acid catalyst such as acid clay, activated clay, silica-alumina, montmolinite type viscosity, or silica gel is used, and an oxygen-containing catalyst such as water, dihydric alcohol, or ether is used. This reaction can be easily carried out by using a compound as a reaction regulator and reacting α-methylstyrene under heating. In addition, the nuclear hydrogenation reaction is performed by using a nuclear hydrogenation catalyst such as nickel, nickel-diatomaceous earth, Raney-nickel, platinum, platinum-alumina, rhodium, rhodium-alumina, etc. This can be easily done by contacting with hydrogen. Depending on the conditions, the polycyclohexylalkane obtained by the above method may have a structure other than the component () of the present invention (dicyclohexylalkane,
Pentacyclohexylalkanes, cyclic compounds, etc.) may also be mixed in as by-products, so if necessary, the target compound can be extracted by separation operations such as distillation. In the traction drive fluid composition of the present invention, the mixing ratio of components () and () is as follows:
The proportion of component () is 80 to 20% by weight, preferably 70 to 30% by weight, relative to 20 to 80% by weight, preferably 30 to 70% by weight of component (). If the mixing ratio of component () is less than the above range, the viscosity of the composition becomes too high, and in particular, component () alone is semi-solid at room temperature and cannot be put to practical use. On the other hand, if the mixing ratio of component () exceeds the above range, the high temperature properties and traction coefficient of the composition will decrease, which is not preferable. In the present invention, a traction drive fluid with excellent various performances can be obtained by mixing the above-mentioned components () and () in a specific ratio, but the 2,4- It can also contain dicyclohexyl-2-methylpentane. The content of this 2,4-dicyclohexyl-2-methylpentane is arbitrary, but usually 100 parts by weight or less per 100 parts by weight of polycyclohexylalkane, which is the component ().
Preferably it is 50 parts by weight or less. When this 2,4-dicyclohexyl-2-methylpentane is used in combination, the components () and () of the present invention are mixed to obtain the fluid composition for traction drive according to the present invention, and then 2,4-dicyclohexyl-2-methylpentane is used. -dicyclohexyl-2-methylpentane may be mixed. Furthermore, as mentioned above, when producing component () by polymerizing α-methylstyrene, depending on the reaction conditions, in addition to component (), 2,4-dicyclohexyl-
Since 2-methylpentane is also produced as a by-product, the by-produced 2,4-dicyclohexyl-2-methylpentane may be mixed with component () in the form of a mixture with component () without being separated and removed. Furthermore, as mentioned above, when producing component () by polymerizing α-methylstyrene, depending on the reaction conditions, a cyclic compound (α-
Nuclear hydrogenated products of cyclic dimers, cyclic trimers, and cyclic tetramers of methylstyrene may also be produced as by-products, but these cyclic compounds can also be used in the process of the present invention to the extent that they do not impair the effects of the present invention. It may be included in the fluid composition for shock driving. Furthermore, various commonly used lubricating oil additives can be added to the traction drive fluid composition of the present invention, if necessary. Specifically, for example, hindered phenols such as 2,6-di-t-butyl-p-cresol, aromatic amines such as phenyl-α-naphthylamine, organometallic compounds such as zinc dialkyldithiophosphate, sulfides, and disulfides. Antioxidants such as sulfur compounds such as carboxylic acids, sulfonic acids, phosphates, amines, alcohols, rust inhibitors such as esters, organic sulfur compounds, organic halogen compounds, etc.
Organic metal salts such as zinc dialkyldithiophosphate, molybdenum dialkyldithiophosphate, and molybdenum dialkyldithiocarbamate, extreme pressure agents such as phosphate esters, polymethacrylate,
Viscosity index improvers such as polyisobutylene, antifoaming agents such as silicone oil, etc. can be added. Although the amount of these known lubricating oil additives added is arbitrary, it is usually desirable to add them so that the total amount added is 20% by weight or less, preferably 10% by weight or less, based on the total amount of the composition. . Furthermore, known organic or inorganic thickeners for greases, specifically soap-based thickeners such as lithium soap, sodium soap, calcium soap, lithium complex soap, calcium complex soap, Complex soap thickeners such as aluminum complex soaps, non-soap thickeners such as organic siloxanes, terephthalamates, polyureas, organically treated clays, and silica aerogels can be added to the traction drive fluid composition of the present invention. It can also be mixed and used as a traction grease. The amount of thickening agent mixed when used as a traction grease is arbitrary, but the content of thickening agent is usually 1 to 1% based on the total amount of the grease composition.
It is preferable to mix it so that it is 30% by weight, preferably 3 to 20% by weight. EXAMPLES OF THE INVENTION The contents of the present invention will now be explained in more detail with reference to Examples and Comparative Examples. Examples 1 to 4 and Comparative Examples 1 to 5 Traction drive fluid compositions (Examples 1 to 4) according to the present invention were obtained with the compositions shown in Table 1. In addition, each component shown in Table 1 has the following properties. () Component squalane: A substance whose main component is 2,6,10,15,19,23-hexamethyltetracosane obtained by further hydrogenating squalane obtained from shark liver oil. viscosity
18.9cSt (@40℃), pour point -65℃ or less, flash point 230
°C, average molecular weight 423. Polybutene 1: Isobutylene-1-butene copolymer obtained by low polymerization of the butane-butene fraction produced by naphtha decomposition. Kinematic viscosity 2.7cSt (@40℃), pour point -70
℃ or less, flash point 87℃, average molecular weight 220. Polybutene 2: Isobutylene-1-butene copolymer obtained by low polymerization of the butane-butene fraction produced by naphtha decomposition. Kinematic viscosity 7.5cSt (@40℃), pour point -
67.5℃, flash point 115℃, average molecular weight 280. 1-decene oligomer: A branched hydrocarbon compound obtained by low polymerization of 1-decene. Kinematic viscosity 17.5cSt (@40℃), pour point -73℃, flash point 216℃, average molecular weight 353. () Component polycyclohexylalkane: A distillate with a boiling point of 415 to 430°C (converted to normal pressure) obtained by nuclear hydrogenation of a product obtained by polymerizing α-methylstyrene using activated clay as a catalyst using a nickel catalyst, and then distilling the product. minutes, is semi-solid at room temperature (20℃),

【化】 R1CH3、R2たたは R1、R2CH3 を䞻成分含量95重量ずする。実斜䟋〜
の組成物に぀いお、以䞋に瀺す性胜評䟡詊隓を行
い、その結果も衚に瀺した。 性胜評䟡詊隓 高枩粘床 JIS  2283.3に芏定する動粘床詊隓方法に準
じお100℃での動粘床を枬定した。 蒞発損倱量 JIS  2540に芏定する最滑油熱安定床詊隓方
法に準じお10℃で100時間加熱埌、油の蒞発損倱
量重量枛を重量で求めた。 トラクシペン係数 四円筒ころがり摩擊詊隓機を甚い、1500rpm、
荷重92.5Kgmm2、すべり率の条件で枬定し
た。 たた比范のため、成分のみを甚いた堎合
比范䟋〜およびトラクシペンドラむブ甚
流䜓ずしお広く甚いられおいる−ゞシクロ
ヘキシル−−メチルペンタンを甚いた堎合比
范䟋に぀いおも䞊蚘の性胜評䟡詊隓を行い、
その結果も衚に䜵蚘した。
[Chemical formula] (R 1 = CH 3 , R 2 = H or R 1 = H, R 2 = CH 3 ) is the main component (content 95% by weight). Examples 1-4
The following performance evaluation test was conducted on the composition, and the results are also shown in Table 1. Performance Evaluation Test [High Temperature Viscosity] The kinematic viscosity at 100°C was measured according to the kinematic viscosity test method specified in JIS K 2283.3. [Evaporation Loss] After heating at 10° C. for 100 hours according to the lubricating oil thermal stability test method specified in JIS K 2540, the evaporation loss (weight loss) of the oil was determined in weight %. [Traction coefficient] Using a four-cylinder rolling friction tester, 1500 rpm,
Measurements were made under the conditions of a load of 92.5 Kg/mm 2 and a slip ratio of 2%. For comparison, the case where only component () was used (Comparative Examples 1 to 4) and the case where 2,4-dicyclohexyl-2-methylpentane, which is widely used as a traction drive fluid, were used (Comparative Example 5). ) was also subjected to the above performance evaluation test,
The results are also listed in Table 1.

【衚】【table】

【衚】 発明の効果 衚の実斜䟋ず比范䟋〜の性胜評䟡詊隓の
比范から明らかなずおり、成分単独の堎合
に比べお成分を配合するこずによりその高
枩特性が著しく向䞊高枩での粘床が増加し、蒞
発損倱量が枛少し、しかもトラクシペン係数も
向䞊しおおり、単独では実甚に䟛するこずができ
ない成分が成分の配合剀ずしお極め
お有効に䜜甚しおいるこずがわかる。 たた本発明に係る実斜䟋の組成物は、トラクシ
ペンドラむブ甚流䜓ずしお䞀般に䜿甚されおいる
比范䟋の−ゞシクロヘキシル−−メチ
ルペンタンず比べおも特に高枩特性に優れおお
り、トラクシペンドラむブ甚流䜓ずしお有甚であ
る。
[Table] Effects of the Invention As is clear from the comparison of the performance evaluation tests of the Examples in Table 1 and Comparative Examples 1 to 4, the high-temperature properties are significantly improved by blending component () compared to when component () is used alone. (increased viscosity at high temperatures and reduced evaporation loss) and also improved the traction coefficient. Component (), which cannot be put to practical use alone, works extremely effectively as a combination agent of component (). I know what you're doing. Furthermore, the compositions of Examples according to the present invention have particularly excellent high-temperature properties compared to 2,4-dicyclohexyl-2-methylpentane of Comparative Example 5, which is generally used as a traction drive fluid. Useful as a shock drive fluid.

Claims (1)

【特蚱請求の範囲】  () (A) スクワラン、および (B) 炭玠数〜12のオレフむンの少なくずも皮
を単独重合たたは共重合するこずにより埗られ
る、40℃での動粘床が〜40cStか぀平均分子量
が100〜500のポリオレフむン油からなる矀より遞
ばれる皮たたは皮以䞊の鎖状炭化氎玠化合
物、〜80重量、 ならびに () 䞀般匏 【化】 匏䞭、はたたはの敎数を瀺し、R1およ
びR2はR1のずきR2CH3、R1CH3のずき
R2ずなる基をそれぞれ瀺す。で衚わされる
ポリシクロヘキシルアルカン、80〜20重量、 を混合しおなるこずを特城ずするトラクシペンド
ラむブ甚流䜓組成物。
[Scope of Claims] 1 () A polymer having a kinematic viscosity of 2 to 2 at 40°C, obtained by homopolymerizing or copolymerizing at least one of (A) squalane and (B) an olefin having 3 to 12 carbon atoms. 2 to 80% by weight of one or more chain hydrocarbon compounds selected from the group consisting of polyolefin oils having an average molecular weight of 40 cSt and an average molecular weight of 100 to 500, and () general formula [formula] (where n is Indicates an integer of 0 or 1, R 1 and R 2 are R 2 = CH 3 when R 1 = H, and R 2 = CH 3 when R 1 = CH 3
Each group represents a group in which R 2 =H. ) A fluid composition for a traction drive, characterized in that it is made by mixing 80 to 20% by weight of a polycyclohexyl alkane represented by:
JP30922387A 1987-12-07 1987-12-07 Fluid composition for traction drive Granted JPH01149898A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP30922387A JPH01149898A (en) 1987-12-07 1987-12-07 Fluid composition for traction drive
GB8828450A GB2224287B (en) 1987-12-07 1988-12-06 Lubricants for traction drives
DE3841609A DE3841609A1 (en) 1987-12-07 1988-12-07 LUBRICANTS FOR FRICTION CLUTCHES

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP30922387A JPH01149898A (en) 1987-12-07 1987-12-07 Fluid composition for traction drive

Publications (2)

Publication Number Publication Date
JPH01149898A JPH01149898A (en) 1989-06-12
JPH0587117B2 true JPH0587117B2 (en) 1993-12-15

Family

ID=17990415

Family Applications (1)

Application Number Title Priority Date Filing Date
JP30922387A Granted JPH01149898A (en) 1987-12-07 1987-12-07 Fluid composition for traction drive

Country Status (1)

Country Link
JP (1) JPH01149898A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6187979B1 (en) * 1998-11-13 2001-02-13 Idemitsu Kosan Co., Ltd. Lubricating base oil composition and process for producing same
US6372696B1 (en) * 1999-11-09 2002-04-16 The Lubrizol Corporation Traction fluid formulation
HUE042328T2 (en) * 2005-12-12 2019-06-28 Neste Oyj Process for producing a branched hydrocarbon component
DK2270118T3 (en) * 2005-12-12 2019-11-18 Neste Oyj Process for preparing a hydrocarbon component

Also Published As

Publication number Publication date
JPH01149898A (en) 1989-06-12

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