JPH03153799A - Detergent for brake - Google Patents
Detergent for brakeInfo
- Publication number
- JPH03153799A JPH03153799A JP29257089A JP29257089A JPH03153799A JP H03153799 A JPH03153799 A JP H03153799A JP 29257089 A JP29257089 A JP 29257089A JP 29257089 A JP29257089 A JP 29257089A JP H03153799 A JPH03153799 A JP H03153799A
- Authority
- JP
- Japan
- Prior art keywords
- aliphatic
- weight
- carbon atoms
- lower alkyl
- ether
- 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.)
- Granted
Links
- 239000003599 detergent Substances 0.000 title claims abstract description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 30
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 19
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 10
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims abstract description 9
- -1 Exesol D30 Chemical class 0.000 claims abstract description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 19
- 239000012459 cleaning agent Substances 0.000 claims description 13
- 239000002904 solvent Substances 0.000 claims description 8
- 150000005215 alkyl ethers Chemical class 0.000 claims description 7
- 150000002576 ketones Chemical class 0.000 claims description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 abstract description 9
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 abstract description 4
- 125000000217 alkyl group Chemical group 0.000 abstract description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 2
- 235000019441 ethanol Nutrition 0.000 description 20
- 230000000052 comparative effect Effects 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 239000003960 organic solvent Substances 0.000 description 9
- 206010008428 Chemical poisoning Diseases 0.000 description 8
- 230000002265 prevention Effects 0.000 description 8
- 230000033228 biological regulation Effects 0.000 description 7
- HXVNBWAKAOHACI-UHFFFAOYSA-N 2,4-dimethyl-3-pentanone Chemical compound CC(C)C(=O)C(C)C HXVNBWAKAOHACI-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 230000001105 regulatory effect Effects 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 238000004140 cleaning Methods 0.000 description 5
- 239000003208 petroleum Substances 0.000 description 5
- 239000011550 stock solution Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- IIEWJVIFRVWJOD-UHFFFAOYSA-N ethyl cyclohexane Natural products CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 239000012046 mixed solvent Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- JOLQKTGDSGKSKJ-UHFFFAOYSA-N 1-ethoxypropan-2-ol Chemical compound CCOCC(C)O JOLQKTGDSGKSKJ-UHFFFAOYSA-N 0.000 description 2
- QQZOPKMRPOGIEB-UHFFFAOYSA-N 2-Oxohexane Chemical compound CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 244000043261 Hevea brasiliensis Species 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 2
- NGAZZOYFWWSOGK-UHFFFAOYSA-N heptan-3-one Chemical compound CCCCC(=O)CC NGAZZOYFWWSOGK-UHFFFAOYSA-N 0.000 description 2
- 238000013101 initial test Methods 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 229920003052 natural elastomer Polymers 0.000 description 2
- 229920001194 natural rubber Polymers 0.000 description 2
- 235000014593 oils and fats Nutrition 0.000 description 2
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 description 1
- LIPRQQHINVWJCH-UHFFFAOYSA-N 1-ethoxypropan-2-yl acetate Chemical compound CCOCC(C)OC(C)=O LIPRQQHINVWJCH-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- 101100478232 Caenorhabditis elegans spr-3 gene Proteins 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 239000004210 ether based solvent Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- WSGCRAOTEDLMFQ-UHFFFAOYSA-N nonan-5-one Chemical compound CCCCC(=O)CCCC WSGCRAOTEDLMFQ-UHFFFAOYSA-N 0.000 description 1
- 239000003129 oil well Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- FZJCXIDLUFPGPP-UHFFFAOYSA-N propan-2-ol;toluene Chemical compound CC(C)O.CC1=CC=CC=C1 FZJCXIDLUFPGPP-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- FHYUCVWDMABHHH-UHFFFAOYSA-N toluene;1,2-xylene Chemical group CC1=CC=CC=C1.CC1=CC=CC=C1C FHYUCVWDMABHHH-UHFFFAOYSA-N 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/261—Alcohols; Phenols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/43—Solvents
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/50—Solvents
- C11D7/5004—Organic solvents
- C11D7/5022—Organic solvents containing oxygen
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/24—Hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/263—Ethers
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/264—Aldehydes; Ketones; Acetals or ketals
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/266—Esters or carbonates
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Vehicle Cleaning, Maintenance, Repair, Refitting, And Outriggers (AREA)
- Detergent Compositions (AREA)
Abstract
Description
【発明の詳細な説明】
[発明の目的]
(産業上の利用分野)
本発明はブレーキ装置の洗浄剤に関し、更に詳しくは安
全性、洗浄性に優れ特に車両等のブレーキ装置の回転体
の洗浄剤として好適なブレーキ装置の洗浄剤に関する。[Detailed Description of the Invention] [Object of the Invention] (Industrial Field of Application) The present invention relates to a cleaning agent for brake equipment, and more specifically, it has excellent safety and cleaning properties, and is particularly suitable for cleaning rotating bodies of brake equipment of vehicles, etc. The present invention relates to a detergent for brake equipment suitable as a detergent.
(従来の技術)
自動車の摩擦ブレーキ装置としては、従来から、ブレー
キライニングをしたブレーキシューをブレーキディスク
やブレーキドラム等の回転体に制動子として作用きせる
ものが一般に用いられている。(Prior Art) As a friction brake device for an automobile, one in which a brake shoe with a brake lining acts as a brake on a rotating body such as a brake disc or a brake drum has been generally used.
このブレーキライニング材料等から発生する粉塵等がブ
レーキディスク等に付着してブレーキの作動に悪影響を
及ぼすことを避けるため、また、ブレーキライニングに
使用きれているアスベストの粉塵が作業者に悪影響を及
ぼざない様、従来からブレーキ装置専用の洗浄剤が開発
され使用きれている。In order to prevent dust generated from this brake lining material etc. from adhering to brake discs etc. and having a negative effect on brake operation, we also prevent dust from asbestos used in brake lining from having a negative impact on workers. To avoid this problem, detergents specifically designed for brake equipment have been developed and are no longer in use.
このようなブレーキ装置の洗浄剤としては、トルエン、
キシレンもしくは1.1.1−トリクロロエタンなどの
炭化水素系溶剤または塩素化炭化水素系溶剤とメタノー
ル、エタノール等のアルコール系溶剤との混合溶剤(特
公昭58−44118)や1.1.2−トリクロロ−1
,2,2−トリフルオロエタン(以下フロン113とい
う)とメタノール、イソプロピルアルコール等との混合
溶剤が知られている。Toluene,
A mixed solvent of a hydrocarbon solvent such as xylene or 1.1.1-trichloroethane or a chlorinated hydrocarbon solvent and an alcohol solvent such as methanol or ethanol (Japanese Patent Publication No. 58-44118) or 1.1.2-trichloro -1
, 2,2-trifluoroethane (hereinafter referred to as Freon 113) and methanol, isopropyl alcohol, etc. are known as mixed solvents.
(発明が解決しようとする課題)
しかし上記の如き洗浄剤の組合せでは有機溶剤中毒予防
規則で使用が規制されたり、消防法により保管場所、保
管数量が厳しく規制されたり(第四類第−石油類)、ま
た有機溶剤中毒予防規則や消防法では規制されなくとも
オゾン層破壊による地球規模での環境破壊につながるな
ど、その使用に際し厳しく使用が制限きれるものが多い
。(Problem to be solved by the invention) However, the use of the above-mentioned cleaning agent combinations is regulated by the organic solvent poisoning prevention regulations, and the storage location and storage quantity are strictly regulated by the Fire Service Act (Category 4 - Petroleum ), and even if they are not regulated by the Organic Solvent Poisoning Prevention Ordinance or the Fire Service Act, there are many products whose use is severely restricted, such as because they lead to global environmental damage due to ozone layer depletion.
従って、ブレーキ装置の洗浄性に優れ、且つ有機溶剤中
毒予防規則に規制されず、消防法でも第四類第二石油類
以下の規制で使用、保管に関して安全性が高く無公害な
洗浄剤の提供が要望されている。Therefore, we provide a cleaning agent that has excellent cleaning properties for brake equipment, is not regulated by organic solvent poisoning prevention regulations, is regulated under the Fire Service Act, and is safe and non-polluting for use and storage. is requested.
また、近年は有機溶剤中毒予防規則の規制はもとより、
ブレーキ装置を洗浄後すぐに組み込む作業時間の短縮化
傾向により、洗浄剤の乾燥時間が大きな問題となってい
る。In addition, in recent years, in addition to the regulations for the prevention of organic solvent poisoning,
Due to the tendency to shorten the work time required to assemble the brake equipment immediately after cleaning, the drying time of the cleaning agent has become a major problem.
従来の洗浄剤は、有機溶剤中毒予防規則をクリアする為
に乾燥の遅い洗浄剤が多く、組み込み後洗浄剤がブレー
キ装置内に完全に乾燥しないまま残っており、これがブ
レーキ鳴きの原因ともなっている。従って、乾燥速度の
速い洗浄剤が要望されている。Conventional cleaning agents often dry slowly in order to comply with organic solvent poisoning prevention regulations, and after installation, the cleaning agent remains in the brake system without completely drying, which is also the cause of brake squeal. . Therefore, there is a demand for cleaning agents that dry quickly.
(課題を解決するための手段)
本発明者は上記の如き、従来技術の問題点を解決すべく
鋭意研究の結果、ある種の有機溶剤を組合せることによ
って、上記の要望に応えることを知見して本発明を完成
した。(Means for Solving the Problems) As a result of intensive research to solve the problems of the prior art as described above, the present inventor found that the above needs could be met by combining certain organic solvents. The present invention was completed.
すなわち、本発明は炭素数8〜11の脂肪族炭化水素を
ベースに、脂肪族二価アルコールモノ低級アルキエーテ
ル、脂肪族二価アルコールモノ低級アルキエーテルアセ
テートと炭素数1〜4の脂肪族一価アルコールとを組合
せてなるブレーキ装置の洗浄剤である。That is, the present invention is based on an aliphatic hydrocarbon having 8 to 11 carbon atoms, an aliphatic dihydric alcohol mono-lower alkyl ether, an aliphatic dihydric alcohol mono-lower alkyl ether acetate, and an aliphatic monovalent ether having 1 to 4 carbon atoms. This is a detergent for brake equipment made in combination with alcohol.
本発明のブレーキ装置の洗浄剤成分である炭素数8〜1
1の脂肪族炭化水素としては、イソパラフィン(炭素数
9〜11)、ノルマルパラフィン(炭素数8〜11)及
びエチルシロクヘキサン等のナフテン類がある。8 to 1 carbon atoms as the detergent component of the brake device of the present invention
Examples of the aliphatic hydrocarbons in No. 1 include isoparaffins (having 9 to 11 carbon atoms), normal paraffins (having 8 to 11 carbon atoms), and naphthenes such as ethylsiloxhexane.
これらの中には、有機溶剤中毒予防規則に該当せず、人
体に対する影響も少なく、また、油脂類に対する溶解性
が高いという特性を有しているものも少なくない。Among these, there are many that do not fall under the organic solvent poisoning prevention regulations, have little effect on the human body, and have high solubility in oils and fats.
かかる脂肪族炭化水素に配合される脂肪族一価のアルコ
ールとしてはメチルアルコール、エチルアルコール、イ
ソプロピルアルコール、ノルマルプロピルアルコール等
があり、これらの脂肪族一価アルコールを上記のパラフ
ィン系炭化水素に配合した組成物は鉱物系グリス及び合
成油をよく溶かし、アルコールとしてエチルアルコール
、ノルマルプロピルアルコールを用いれば有機溶剤中毒
予防規則にも規制されない。この場合アルコールの含有
量は20%未満にとどめることがこの組成物を第二石油
類とするために必要である。Examples of aliphatic monohydric alcohols that can be blended with such aliphatic hydrocarbons include methyl alcohol, ethyl alcohol, isopropyl alcohol, and normal propyl alcohol. The composition dissolves mineral grease and synthetic oil well, and if ethyl alcohol or n-propyl alcohol is used as the alcohol, it is not regulated by organic solvent poisoning prevention regulations. In this case, it is necessary to keep the alcohol content to less than 20% in order to make this composition a secondary petroleum.
上記したパラフィン系炭化水素に配合される脂肪族二価
アルコールモノ低級アルキルエーテルまたは脂肪族二価
アルコールモノ低級アルキルエーテルアセテートを構成
する脂肪族二価アルコールとしてはモノエチレングリコ
ール、ジエチレングリコール、プロピレングリコール等
がある。The aliphatic dihydric alcohols constituting the aliphatic dihydric alcohol mono-lower alkyl ether or aliphatic dihydric alcohol mono-lower alkyl ether acetate blended with the above-mentioned paraffinic hydrocarbons include monoethylene glycol, diethylene glycol, propylene glycol, etc. be.
低級アルキルエーテル、低級アルキルエーテルアセテー
トの低級アルキル基としては炭素数1〜6のアルキル基
、例えばメチル、エチル、プロピル、ブチル等がある。The lower alkyl group of the lower alkyl ether and lower alkyl ether acetate includes alkyl groups having 1 to 6 carbon atoms, such as methyl, ethyl, propyl, butyl, and the like.
上記の脂肪族二価アルコールのモノ低級アルキルエーテ
ルまたはモノ低級アルキルエーテルアセテート類として
はモノエチレングリコールモノメチルエーテル、モノエ
チレングリコールモノエチルエーテル、モノエチレング
リコールモノブチルエーテル及びモノエチレングリコー
ルモノエチルエーテルアセテート、プロピレングリコー
ルモノメチルエーテル、プロピレングリコールモノエチ
ルエーテル、プロピレングリコールモノメチルエーテル
アセテート、プロピレングリコールモノエチルエーテル
アセテート等があり、合計炭素数5〜10の化合物が特
に好ましく用いられる。Mono-lower alkyl ethers or mono-lower alkyl ether acetates of the above aliphatic dihydric alcohols include monoethylene glycol monomethyl ether, monoethylene glycol monoethyl ether, monoethylene glycol monobutyl ether, monoethylene glycol monoethyl ether acetate, propylene glycol Examples include monomethyl ether, propylene glycol monoethyl ether, propylene glycol monomethyl ether acetate, propylene glycol monoethyl ether acetate, and compounds having a total carbon number of 5 to 10 are particularly preferably used.
これらの脂肪族二価アルコールモノ低級アルキルエーテ
ルや脂肪族二価アルコールモノ低級アルキルエーテルア
セテートは鉱物油や合成油を比較的よく溶かし引火点も
21℃以上で第二石油類に属し蒸発速度も比較的速く、
上記したパラフィン系炭化水素に配合して得られる混合
溶剤はブレーキ装置の洗浄剤として粉塵や油類をよく洗
い流し、人体に対する影響も少なく、引火点も21℃以
上で消防法上も危険物第四類第二石油類に分類される洗
浄剤となる。These aliphatic dihydric alcohol mono-lower alkyl ethers and aliphatic dihydric alcohol mono-lower alkyl ether acetates dissolve mineral oils and synthetic oils relatively well, have a flash point of 21°C or higher, belong to the second class of petroleum, and their evaporation rates are also compared. Quickly,
The mixed solvent obtained by blending with the paraffinic hydrocarbon mentioned above is a cleaning agent for brake equipment that thoroughly washes away dust and oil, has little effect on the human body, has a flash point of 21°C or higher, and is classified as a dangerous substance according to the Fire Service Act. It is a cleaning agent classified as class 2 petroleum.
これら成分の配合割合は、炭素数8〜11の脂肪族炭化
水素20〜30重量部:脂肪族二価アルコールモノ低級
アルキルエーテル及び/又は脂肪族二価アルコールモノ
低級アルキルエーテルアセテート40〜70重量部:炭
素数1〜4の脂肪族一価アルコール5〜20が好ましい
。The mixing ratio of these components is 20 to 30 parts by weight of aliphatic hydrocarbon having 8 to 11 carbon atoms: 40 to 70 parts by weight of aliphatic dihydric alcohol mono-lower alkyl ether and/or aliphatic dihydric alcohol mono-lower alkyl ether acetate. : Aliphatic monohydric alcohol having 1 to 4 carbon atoms, preferably 5 to 20 carbon atoms.
炭素数8〜11の脂肪族炭化水素の使用割合が30%を
越すとゴムに対する侵食性が大きくなり、20%以下で
あると油脂類に対する洗浄力が低下する。また、適度の
乾燥性を有する為には炭素数8〜11のものが適する。If the proportion of aliphatic hydrocarbons having 8 to 11 carbon atoms used exceeds 30%, the erosivity to rubber increases, and if it does not exceed 20%, the detergency against oils and fats decreases. Further, in order to have appropriate drying properties, those having 8 to 11 carbon atoms are suitable.
また、炭素数5〜9のケトン系溶剤又は、炭素数5〜9
のエーテル系溶剤を配合すると有効である。具体的には
、メチルエチルケトン、メチルn−プロピルケトン、メ
チルn−ブチルケトン、メチルイソブチルケトン、メチ
ルn−アミルケトン。Also, a ketone solvent having 5 to 9 carbon atoms or a ketone solvent having 5 to 9 carbon atoms
It is effective to mix this with an ether solvent. Specifically, methyl ethyl ketone, methyl n-propyl ketone, methyl n-butyl ketone, methyl isobutyl ketone, methyl n-amyl ketone.
ジエチルケトン、エチルn−ブチルケトン、ジイソブチ
ルケトン、ジn−ブピルケトン、ジイソプロピルケトン
、ジプロピルエーテル、ジブチルエーテル等があり、ジ
イソプロピルケトン、ジブチルエーテルが消防法、乾燥
速度の面で好ましい。Examples include diethyl ketone, ethyl n-butyl ketone, diisobutyl ketone, di-n-butyl ketone, diisopropyl ketone, dipropyl ether, dibutyl ether, and diisopropyl ketone and dibutyl ether are preferred in terms of fire regulations and drying speed.
ケトン系及びエーテル系溶剤は、蒸発速度を上げる点で
有利であるが、配合量が20%を越すと、ゴムに対する
侵食性が大きくなるので、それ以下におきえるべきであ
る。Ketone and ether solvents are advantageous in terms of increasing the evaporation rate, but if their blending amount exceeds 20%, they become more erosive to rubber, so they should be kept below that amount.
(実施例)
次に実施例及び比較例によって本発明を説明する。なお
配合割合は重量部である。(Example) Next, the present invention will be explained with reference to Examples and Comparative Examples. Note that the blending ratio is in parts by weight.
試験方法
(1)溶解性(洗浄性)
実施例及び比較例で示す各種組成物の原液2゜11を試
験管にとり下記に示すオイル類を各2alその原液の中
に添加し相溶するかどうかを目視にて観察する。Test method (1) Solubility (cleanability) Take 2.11 stock solutions of the various compositions shown in the Examples and Comparative Examples in a test tube, add 2.11 of each of the following oils to the stock solution, and check whether they are compatible. Visually observe.
判定
透明に相溶したもの ○
相溶するが濁ったもの Δ
全く相溶しないもの X
試験体
1)エンジンオイル鉱物系
2)エンジンオイル合成油系
3)ブレーキフルード
4)ギヤオイル
(2)原液のゴムに対する影響
ゴムのテストピース2X25X100mmの重量を計り
その試験片を実施例、比較例で示す各種組成物原液中に
室温(25℃)で30分間浸漬し、その後取り出してウ
ェスで完全に原液を拭き取りその試験片の重量を計り次
の式により重量変化率を計算する。Judgment Transparent and compatible ○ Compatible but cloudy Δ Not compatible at all Weighed a rubber test piece measuring 2 x 25 x 100 mm, immersed the test piece in the various composition stock solutions shown in Examples and Comparative Examples at room temperature (25°C) for 30 minutes, then took it out and wiped the stock solution completely with a rag. Weigh the test piece and calculate the weight change rate using the following formula.
浸漬後の試験片重量−初期の試験片重量初期の試験片重
量
試験体
1)天然ゴム(NR)
2)SPR
3)NBR
4)EPDM
(3)乾燥性
ブレーキライニングのライニング表面を上部に向け、各
種組成物原液20m1をライニング全面に均一に塗布す
る。その後、全面乾燥するまでの時間を測定する。Test piece weight after immersion - Initial test piece weight Initial test piece weight Test piece 1) Natural rubber (NR) 2) SPR 3) NBR 4) EPDM (3) The lining surface of the drying brake lining faces upward, 20 ml of stock solutions of various compositions are uniformly applied to the entire surface of the lining. Then, measure the time until the entire surface dries.
(4)引火点(消防法区分)
実施例および比較例の各種組成物の引火点をタグ密閉式
引火点測定機にて測定。(4) Flash point (Fire Service Act classification) The flash point of various compositions of Examples and Comparative Examples was measured using a sealed tag flash point measuring device.
実施例1〜4.比較例1〜5 次の組成の洗浄剤を調整した。Examples 1-4. Comparative examples 1 to 5 A cleaning agent with the following composition was prepared.
実施例1
エクセゾールD30 30重量部(エクソ
ン化学(株)炭素数9〜10のナフテンとイソパラフィ
ンの混合物)
プロピレングリコールモノメチルエーテル60重量部
ノルマルプロピルアルコール IC3重量部実施例
2
エクセゾールD30 30重量部(エクソ
ン化学(株)炭素数9〜10のナフテンとイソバラフィ
シの混合物)
プロピレングリコールモノメチルエーテル50重量部
ノルマルプロピルアルコール 20重量部実施例3
ノルマルパラフィン(C=10) 20重量部プロピ
レングリコールモノエチルエーテル60重量部
ノルマルプロピルアルコール 10重量部ジイソプ
ロピルケトン 10重量部実施例4
エチルシクロヘキサン 20重量部プロピレ
ングリコールモノメチルエーテル60重量部
ノルマルプロピルアルコール 10重量部ノルマル
ブチルエーテル 10重量部比較例1
エチルシクロヘキサン
比較例2
トルエン
イソプロピルアルコール
比較例3
1・1・1−トリクロロエタン
エタノール
比較例4
トルエン
キシレン
比較例5
ミネラルスピリット
100重量部
20重量部
80重量部
65重量部
35重量部
50重量部
50重量部
100重量部
表(1)から明かなように本発明によりブレーキ装置の
洗浄剤は良好な洗浄力、乾燥性、消防法上の第二石油類
、有機溶剤中毒予防規則の適用外であり、安全な洗浄剤
であり、その実用的効果は顕著である。Example 1 Exesol D30 30 parts by weight (Exxon Chemical Co., Ltd.) Mixture of naphthenes having 9 to 10 carbon atoms and isoparaffin) Propylene glycol monomethyl ether 60 parts normal propyl alcohol IC 3 parts by weight Example 2 Exesol D30 30 parts by weight (Exxon Chemical Co., Ltd.) (Mixture of naphthene having 9 to 10 carbon atoms and isobarafishi) Propylene glycol monomethyl ether 50 parts by weight Normal propyl alcohol 20 parts by weight Example 3 Normal paraffin (C=10) 20 parts by weight Propylene glycol monoethyl ether 60 parts by weight Normal Propyl alcohol 10 parts by weight Diisopropyl ketone 10 parts by weight Example 4 Ethylcyclohexane 20 parts by weight Propylene glycol monomethyl ether 60 parts by weight Normal propyl alcohol 10 parts by weight Normal butyl ether 10 parts by weight Comparative example 1 Ethylcyclohexane comparative example 2 Toluene Isopropyl alcohol comparative example 3 1.1.1-Trichloroethane Ethanol Comparative Example 4 Toluene xylene Comparative Example 5 Mineral spirit 100 parts by weight 20 parts by weight 80 parts by weight 65 parts by weight 35 parts by weight 50 parts by weight 50 parts by weight 100 parts by weight As is clear from Table (1) According to the present invention, the cleaning agent for brake equipment has good cleaning power, drying properties, is not applicable to the second petroleum class under the Fire Service Act, and is not subject to the Organic Solvent Poisoning Prevention Ordinance, and is therefore a safe cleaning agent, and its practical effects are Remarkable.
Claims (1)
ルコールモノ低級アルキルエーテル及び/又は脂肪族二
価アルコールモノ低級アルキルエーテルアセテート、炭
素数1〜4の脂肪族一価アルコールからなるブレーキ装
置の洗浄剤。 2 炭素数5〜9のケトン系溶剤又は、炭素数5〜9の
エーテル系溶剤を配合してなる請求項1記載のブレーキ
装置の洗浄剤。[Scope of Claims] 1. An aliphatic hydrocarbon having 8 to 11 carbon atoms, an aliphatic dihydric alcohol mono-lower alkyl ether and/or an aliphatic dihydric alcohol mono-lower alkyl ether acetate, and an aliphatic hydrocarbon having 1 to 4 carbon atoms. Brake device cleaning agent made of monohydric alcohol. 2. The detergent for brake equipment according to claim 1, which contains a ketone solvent having 5 to 9 carbon atoms or an ether solvent having 5 to 9 carbon atoms.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1292570A JP2802656B2 (en) | 1989-11-10 | 1989-11-10 | Cleaning agent for brake equipment |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1292570A JP2802656B2 (en) | 1989-11-10 | 1989-11-10 | Cleaning agent for brake equipment |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03153799A true JPH03153799A (en) | 1991-07-01 |
JP2802656B2 JP2802656B2 (en) | 1998-09-24 |
Family
ID=17783483
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1292570A Expired - Fee Related JP2802656B2 (en) | 1989-11-10 | 1989-11-10 | Cleaning agent for brake equipment |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2802656B2 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5370817A (en) * | 1990-11-15 | 1994-12-06 | Lockheed Corporation | Low odor cleaning formulation comprising propylene glycol methyl ether and propylene glycol methyl ether acetate |
WO1996033261A1 (en) * | 1995-04-20 | 1996-10-24 | Elf Atochem S.A. | Cold cleaning composition based on alkanes or cycloalkanes and an organic compound comprising a ketone group |
US5643860A (en) * | 1994-05-06 | 1997-07-01 | Comstar International, Inc. | Cleaning composition for pipes and coils of a refrigeration system |
JPH11302696A (en) * | 1998-04-24 | 1999-11-02 | Yokohama Yushi Kogyo Kk | Aqueous detergent composition for pressure spraying and cleaning method |
JP2007217705A (en) * | 2007-03-30 | 2007-08-30 | Japan Energy Corp | Hydrocarbon-based cleaning liquid composition |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0352987A (en) * | 1989-07-20 | 1991-03-07 | Tsuchiya:Kk | Aerosol agent for cleansing automotive brake device |
JPH03131699A (en) * | 1989-10-17 | 1991-06-05 | Tsuchiya:Kk | Cleaning method for automotive braking device |
-
1989
- 1989-11-10 JP JP1292570A patent/JP2802656B2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0352987A (en) * | 1989-07-20 | 1991-03-07 | Tsuchiya:Kk | Aerosol agent for cleansing automotive brake device |
JPH03131699A (en) * | 1989-10-17 | 1991-06-05 | Tsuchiya:Kk | Cleaning method for automotive braking device |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5370817A (en) * | 1990-11-15 | 1994-12-06 | Lockheed Corporation | Low odor cleaning formulation comprising propylene glycol methyl ether and propylene glycol methyl ether acetate |
US5643860A (en) * | 1994-05-06 | 1997-07-01 | Comstar International, Inc. | Cleaning composition for pipes and coils of a refrigeration system |
WO1996033261A1 (en) * | 1995-04-20 | 1996-10-24 | Elf Atochem S.A. | Cold cleaning composition based on alkanes or cycloalkanes and an organic compound comprising a ketone group |
FR2733248A1 (en) * | 1995-04-20 | 1996-10-25 | Atochem Elf Sa | COLD CLEANING COMPOSITION BASED ON ALKANES OR CYCLOALKANES AND AN ORGANIC COMPOUND COMPRISING AN OXYGENIC FUNCTION |
US6162779A (en) * | 1995-04-20 | 2000-12-19 | Elf Atochem, S.A. | Cold cleaning composition based on alkanes or cycloalkanes and an organic compound comprising a ketone group |
JPH11302696A (en) * | 1998-04-24 | 1999-11-02 | Yokohama Yushi Kogyo Kk | Aqueous detergent composition for pressure spraying and cleaning method |
JP2007217705A (en) * | 2007-03-30 | 2007-08-30 | Japan Energy Corp | Hydrocarbon-based cleaning liquid composition |
JP4671984B2 (en) * | 2007-03-30 | 2011-04-20 | Jx日鉱日石エネルギー株式会社 | Hydrocarbon cleaning liquid composition |
Also Published As
Publication number | Publication date |
---|---|
JP2802656B2 (en) | 1998-09-24 |
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