WO2013046755A1 - クロスヘッド型ディーゼル機関用シリンダー潤滑油組成物 - Google Patents
クロスヘッド型ディーゼル機関用シリンダー潤滑油組成物 Download PDFInfo
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M141/00—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
- C10M141/08—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic sulfur-, selenium- or tellurium-containing compound
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M141/00—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
- C10M141/06—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic nitrogen-containing compound
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M163/00—Lubricating compositions characterised by the additive being a mixture of a compound of unknown or incompletely defined constitution and a non-macromolecular compound, each of these compounds being essential
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/26—Carboxylic acids; Salts thereof
- C10M129/48—Carboxylic acids; Salts thereof having carboxyl groups bound to a carbon atom of a six-membered aromatic ring
- C10M129/50—Carboxylic acids; Salts thereof having carboxyl groups bound to a carbon atom of a six-membered aromatic ring monocarboxylic
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/26—Carboxylic acids; Salts thereof
- C10M129/48—Carboxylic acids; Salts thereof having carboxyl groups bound to a carbon atom of a six-membered aromatic ring
- C10M129/54—Carboxylic acids; Salts thereof having carboxyl groups bound to a carbon atom of a six-membered aromatic ring containing hydroxy groups
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/38—Heterocyclic nitrogen compounds
- C10M133/44—Five-membered ring containing nitrogen and carbon only
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
- C10M135/08—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium containing a sulfur-to-oxygen bond
- C10M135/10—Sulfonic acids or derivatives thereof
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/1006—Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/108—Residual fractions, e.g. bright stocks
- C10M2203/1085—Residual fractions, e.g. bright stocks used as base material
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/028—Overbased salts thereof
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/26—Overbased carboxylic acid salts
- C10M2207/262—Overbased carboxylic acid salts derived from hydroxy substituted aromatic acids, e.g. salicylates
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/28—Amides; Imides
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/046—Overbasedsulfonic acid salts
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/04—Molecular weight; Molecular weight distribution
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/04—Detergent property or dispersant property
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/06—Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/252—Diesel engines
Definitions
- the present invention relates to a cylinder lubricant composition for a crosshead type diesel engine.
- ⁇ Crosshead diesel engines use cylinder oil that lubricates between the cylinder and piston, and system oil that controls lubrication and cooling of other parts.
- the cylinder oil is required to have the proper viscosity necessary for lubrication between the cylinder and the piston (piston ring) and the function of maintaining the cleanliness necessary for proper movement of the piston and piston ring. It is done.
- the high-sulfur fuel is usually used in the crosshead type diesel engine because of its economical efficiency, it has a problem of cylinder corrosion due to acidic components such as sulfuric acid generated by combustion.
- the cylinder oil also needs a function of neutralizing acidic components such as sulfuric acid to be generated and preventing corrosion.
- the cylinder diameter is increased (for example, bore size is 70 cm or more) and the piston stroke is increased (for example, average piston speed is 8 m / s or more).
- an increase in combustion pressure for example, net average effective pressure (BMEP) of 1.8 MPa or more
- BMEP net average effective pressure
- the increase in combustion pressure causes an increase in the dropping point of sulfuric acid. Corrosion is more likely to occur.
- the wall temperature of the cylinder is increased (for example, the cylinder wall temperature is 250 ° C. or more), and the amount of lubricating oil injected into the cylinder is being reduced for economic reasons. As a result, the lubrication environment of cylinders is becoming more severe.
- the IMO International Maritime Organization
- the IMO International Maritime Organization
- fuel with a sulfur content of 4.5% by mass or less even in high-sulfur fuel in general sea areas and low-sulfur fuel with 1% by mass or less of fuel sulfur must be used in regulated sea areas centering on the North Sea. Is no longer.
- Patent Documents 1 to 5 Many conventional cylinder oils have low-cost base oils with overbased sulfonate metal detergents as the main component to maintain corrosion wear resistance, but recently, salicylate, phenate or There have been developed various types of metal detergents such as composite detergents as main components and further containing an extreme pressure agent and a dispersant (Patent Documents 1 to 5).
- the present invention has no problem with any sulfur amount fuel in addition to conventional performance such as heat resistance, cleanliness, wear resistance, etc. as a cylinder lubricant for a crosshead type diesel engine.
- An object of the present invention is to provide a cylinder lubricant for a crosshead type diesel engine in which the piston deposit amount is suppressed even when the base number is excessive.
- the present inventors contain an ashless dispersant and a metallic detergent, and the product of the number average molecular weight, the blending amount, and the effective concentration of the ashless dispersant is a specific value or more.
- the present inventors have found that a cross-head type diesel engine cylinder lubricating oil composition in which the endothermic peak temperature of the metallic detergent is not more than a specific value can improve the above problems, and have completed the present invention.
- the present invention includes (A) a lubricating base oil containing (B) an ashless dispersant and (C) a metal-based detergent,
- the product of the number average molecular weight, the blending amount and the effective concentration of the (B) ashless dispersant is 9000 or more
- the (C) metal-based detergent is a cylinder lubricant composition for a crosshead type diesel engine having an endothermic peak temperature of 460 ° C. or less at a temperature rising rate of 50 ° C./min as measured by DSC. .
- the number average molecular weight of the ashless dispersant described in (B) is 2500 or more.
- the present invention softens the ash content of the cylinder oil that accumulates on the piston top land and easily breaks down to suppress deposit accumulation on the land portion.
- This is a cylinder lubricating oil composition for a crosshead type diesel engine that can be used in sulfur fuel and gas-fired engines.
- Lubricating oil base oil in the cylinder lubricating oil composition for a crosshead type diesel engine of the present invention is not particularly limited, and is a mineral oil system used for ordinary lubricating oil. Base oils and / or synthetic oil base oils can be used.
- the lubricating oil fraction obtained by subjecting the crude oil to atmospheric distillation obtained under reduced pressure is subjected to solvent removal, solvent extraction, hydrocracking, GTL WAX (Gas Liquid Liquid) produced by one or more treatments such as solvent dewaxing, catalytic dewaxing, hydrorefining, etc., or GTL WAX (Gas Liquid Liquid) produced by wax isomerized mineral oil, Fischer-Tropsch process, etc. is isomerized Examples thereof include a lubricating base oil produced by a technique.
- the total aromatic content of the mineral oil base oil is not particularly limited, but is preferably 40% by mass or less, more preferably 30% by mass or less.
- the total aromatic content of the mineral base oil may be 0% by mass, but is preferably 1% by mass or more, more preferably 5% by mass or more, more preferably 10% by mass or more in terms of the solubility of the additive. More preferably, it is particularly preferably 20% by mass or more.
- oxidation stability is inferior, which is not preferable.
- the said total aromatic content means the aromatic fraction content measured based on ASTM D2549.
- this aromatic fraction includes alkylbenzene, alkylnaphthalene, anthracene, phenanthrene, alkylated products thereof, compounds in which four or more benzene rings are condensed, and heterogeneous compounds such as pyridines, quinolines, phenols, and naphthols. Compounds having aromatics are included.
- the sulfur content in the mineral oil base oil is not particularly limited, but is preferably 1% by mass or less, and more preferably 0.5% by mass or less. Although 0 mass% may be sufficient as the sulfur content in mineral oil type base oil, Preferably it is 0.1 mass% or more, More preferably, it is 0.2 mass% or more. When the mineral oil base oil contains sulfur to some extent, the solubility of the additive can be sufficiently increased.
- synthetic base oil examples include polybutene or hydride thereof; poly ⁇ -olefin or hydride thereof having 8 to 14 carbon atoms represented by 1-octene oligomer, 1-decene oligomer, etc. Diesters such as ditridecyl glutarate, di-2-ethylhexyl adipate, diisodecyl adipate, ditridecyl adipate, di-2-ethylhexyl sebacate; trimethylolpropane caprylate, trimethylolpropane pelargonate, pentaerythritol-2-ethylhexa Polyol esters such as noate and pentaerythritol pelargonate; copolymers of dicarboxylic acids such as dibutyl maleate and ⁇ -olefins having 2 to 30 carbon atoms; fragrances such as alkylnaphthalenes, alkylbenzene
- the (A) lubricating base oil a mineral base oil, a synthetic base oil, or an arbitrary mixture of two or more base oils selected from these can be used.
- examples thereof include one or more mineral oil base oils, one or more synthetic oil base oils, a mixed oil of one or more mineral oil base oils and one or more synthetic oil base oils, and the like.
- the kinematic viscosity of the lubricating base oil to be used is not particularly limited, but the kinematic viscosity at 100 ° C. is preferably 4 to 50 mm 2 / s, more preferably 6 to 40 mm 2 / s, particularly preferably. Is 8 to 35 mm 2 / s. If the kinematic viscosity at 100 ° C.
- the lubricating base oil exceeds 50 mm 2 / s, and deteriorates the low-temperature viscosity characteristic, whereas, when the kinematic viscosity is less than 4 mm 2 / s, oil film formation at lubricating sites Insufficient lubricity results in poor lubricity and increases the evaporation loss of the lubricating base oil, which is not preferable.
- the lubricating base oil may have a kinematic viscosity at 100 ° C. of 4 to less than 17 mm 2 / s and / or a kinematic viscosity at 100 ° C. of 17 to 150 mm 2 / s. It is preferable to contain oil.
- the lubricating base oil having a kinematic viscosity at 100 ° C. of less than 4 to 17 mm 2 / s include mineral base oils such as SAE 10 to 40 and synthetic base oils, and the kinematic viscosity is preferably 5.
- the lubricating base oil having a kinematic viscosity at 100 ° C. of 17 to 50 mm 2 / s include mineral oil base oils and synthetic oil base oils such as SAE50 and bright stock, and the kinematic viscosity is preferably Is 20 mm 2 / s or more, more preferably 25 mm 2 / s or more, preferably 40 mm 2 / s or less, more preferably 35 mm 2 / s or less.
- a synthetic base oil is equivalent.
- the NOACK evaporation amount of the lubricating base oil is preferably 20% by mass or less, more preferably 16% by mass or less, and particularly preferably 10% by mass or less.
- the NOACK evaporation amount of the lubricating base oil exceeds 20% by mass, the evaporation loss of the lubricating oil is large, which causes an increase in viscosity and the like, which is not preferable.
- the NOACK evaporation amount is a value obtained by measuring the evaporation amount of the lubricating oil measured according to ASTM D5800.
- the viscosity index of the lubricating base oil to be used is not particularly limited, but the value is preferably 80 or more, more preferably 90 or more, still more preferably 100 or more so that excellent viscosity characteristics from low temperature to high temperature can be obtained. It is.
- the upper limit of the viscosity index of the lubricating base oil is not particularly limited, and those having a viscosity index of about 135 to 180, such as normal paraffin, slack wax, GTL wax, or isoparaffin mineral oil obtained by isomerizing these, In addition, those having a viscosity index of about 150 to 250 such as complex ester base oil and HVI-PAO base oil can be used, but the viscosity index is 120 in terms of the solubility and storage stability of the additive. Or less, more preferably 110 or less.
- the cylinder lubricating oil composition for a crosshead type diesel engine of the present invention contains (B) an ashless dispersant (hereinafter sometimes referred to as (B) component) as an essential component.
- any ashless dispersant used in lubricating oils can be used.
- at least one nitrogen-containing compound or derivative thereof, a Mannich dispersant, or a modified product of alkenyl succinimide In use, one kind or two or more kinds arbitrarily selected from these can be blended.
- the alkyl group or alkenyl group may be linear or branched, and is preferably a branch derived from an olefin oligomer such as propylene, 1-butene, isobutylene, or a co-oligomer of ethylene and propylene.
- An alkyl group and a branched alkenyl group may be linear or branched, and is preferably a branch derived from an olefin oligomer such as propylene, 1-butene, isobutylene, or a co-oligomer of ethylene and propylene.
- Examples of the component (B) include one or more compounds selected from the following components (B-1) to (B-3).
- B-1) Succinimide having at least one alkyl group or alkenyl group having 40 to 400 carbon atoms in the molecule, or a derivative thereof
- B-2) benzylamine having at least one alkyl group or alkenyl group having 40 to 400 carbon atoms in the molecule, or a derivative thereof
- B-3) A polyamine having at least one alkyl group or alkenyl group having 40 to 400 carbon atoms in the molecule, or a derivative thereof.
- R 1 represents an alkyl or alkenyl group having 40 to 400 carbon atoms, preferably 60 to 350, and h represents an integer of 1 to 5, preferably 2 to 4.
- R 2 and R 3 each independently represents an alkyl group or alkenyl group having 40 to 400 carbon atoms, preferably 60 to 350 carbon atoms, and particularly preferably a polybutenyl group.
- I represents an integer of 0 to 4, preferably 1 to 3.
- the component (B-1) includes a so-called monotype succinimide represented by the formula (1) in which succinic anhydride is added to one end of the polyamine, and a formula in which succinic anhydride is added to both ends of the polyamine (although the so-called bis-type succinimide represented by 2) is included, any of these or a mixture thereof may be included in the composition of the present invention.
- the method for producing the succinimide as the component (B-1) is not particularly limited.
- a compound having an alkyl group or an alkenyl group having 40 to 400 carbon atoms is reacted with maleic anhydride at 100 to 200 ° C. It is obtained by reacting the obtained alkyl succinic acid or alkenyl succinic acid with a polyamine.
- the polyamine include diethylenetriamine, triethylenetetramine, tetraethylenepentamine, and pentaethylenehexamine.
- R 4 represents an alkyl or alkenyl group having 40 to 400 carbon atoms, preferably 60 to 350, and j represents an integer of 1 to 5, preferably 2 to 4.
- the benzylamine which is the said (B-2) component For example, after making polyolefin, such as a propylene oligomer, polybutene, or an ethylene-alpha-olefin copolymer, react with phenol to make alkylphenol, Examples thereof include a method in which formaldehyde and a polyamine such as diethylenetriamine, triethylenetetramine, tetraethylenepentamine, or pentaethylenehexamine are reacted by a Mannich reaction.
- polyolefin such as a propylene oligomer, polybutene, or an ethylene-alpha-olefin copolymer
- formaldehyde and a polyamine such as diethylenetriamine, triethylenetetramine, tetraethylenepentamine, or pentaethylenehexamine are reacted by a Mannich reaction.
- R 5 represents an alkyl group or alkenyl group having 40 to 400 carbon atoms, preferably 60 to 350, and k represents an integer of 1 to 5, preferably 2 to 4.
- polyamine which is the said (B-3) component there is no restriction
- polyolefin such as a propylene oligomer, polybutene, or an ethylene-alpha-olefin copolymer
- this is ammonia, ethylenediamine, diethylenetriamine.
- a method of reacting polyamines such as triethylenetetramine, tetraethylenepentamine, or pentaethylenehexamine.
- Examples of the derivative of the nitrogen-containing compound exemplified as the component (B) include, for example, monocarboxylic acids such as fatty acids having 1 to 30 carbon atoms, oxalic acid, phthalic acid, trimellitic acid, pyromellitic to the nitrogen-containing compounds described above.
- monocarboxylic acids such as fatty acids having 1 to 30 carbon atoms, oxalic acid, phthalic acid, trimellitic acid, pyromellitic to the nitrogen-containing compounds described above.
- the remaining amino group and / or the reaction of a polycarboxylic acid having 2 to 30 carbon atoms such as an acid, or an anhydride thereof, or an ester compound, an alkylene oxide having 2 to 6 carbon atoms, or a hydroxy (poly) oxyalkylene carbonate.
- a remaining amino group by allowing phosphoric acid to act on the aforementioned nitrogen-containing compound A so-called phosphoric acid-modified compound obtained by neutralizing or amidating a part or all of the amino group and / or imino group; a sulfur-modified compound obtained by allowing a sulfur compound to act on the nitrogen-containing compound described above; and a nitrogen-containing compound described above.
- the boric acid-modified compound of alkenyl succinimide particularly the boric acid-modified compound of bis-type alkenyl succinimide, can further improve the heat resistance when used in combination with the above-mentioned component (A). .
- the content ratio of the component (B) in the lubricating oil composition of the present invention is usually 0.005 to 0.4% by mass, preferably 0.01 to 0.2% by mass, as the amount of nitrogen, based on the total amount of the composition. More preferably, the content is 0.01 to 0.1% by mass, and particularly preferably 0.02 to 0.05% by mass.
- the mass ratio (B / N ratio) between the boron content and the nitrogen content is not particularly limited, but preferably 0.5 to 1 More preferably, it is 0.7 to 0.9. The higher the B / N ratio is, the easier it is to improve the wear resistance and seizure resistance.
- the content ratio is not particularly limited, but is preferably 0.001 to 0.1% by mass, more preferably 0.005, as the boron content based on the total amount of the composition. It is preferably 0.05 to 0.05% by mass, particularly preferably 0.01 to 0.04% by mass.
- the component (B) preferably has a boron content of 0.5% by mass or more, more preferably 1.0% by mass or more, still more preferably 1.5% by mass or more, particularly preferably. It is most desirable to include 1.8% by mass of a boron-containing ashless dispersant, in particular, a bis-type boron-containing succinimide-based ashless dispersant.
- the boron-containing ashless dispersant having a boron content of 0.5% by mass or more here includes 10 to 90% by mass, preferably 30 to 70% by mass, for example, a diluent oil such as mineral oil or synthetic oil.
- the boron content usually means the boron content in a state including a diluent oil.
- the number average molecular weight (Mn) of the component (B) in the present invention is measured by removing diluted oil from the sample by rubber membrane fractionation, and analyzing this by GPC (Gel Permeation Chromatography).
- the procedure for rubber membrane dialysis fractionation is as follows.
- (I) Collect about 5 g of sample in the rubber film.
- (Ii) The rubber film is bound with a thread, and the rubber film is placed in a cylindrical filter paper.
- (Iii) Place in a Soxhlet extractor with cylindrical filter paper.
- (Iv) Put 100 ml of petroleum ether in a flat flask, and install a Soxhlet extractor on it.
- V The flat flask is heated in a water bath (70 ° C.), and the Soxhlet extractor is cooled with an attached cooler.
- (Vi) Heat to reflux for 2 days.
- the effective concentration of the ashless dispersant as the component (B) was determined from the result of the rubber membrane dialysis fraction described above. That is, the ratio of the mass remaining in the rubber film with respect to the amount of sample (about 5 g) collected as a sample first was taken as the effective concentration.
- the ashless dispersant such that the product of its number average molecular weight (Mn), blending amount and effective concentration is 9000 or more, which is preferably 10,000 or more, More preferably, it is 12000 or more, More preferably, it is 15000 or more, Most preferably, it is 20000 or more, However, It is preferable that it is 50000 or less. If the product is less than 9000, the deposit intended in the present invention is not easily broken, not only the deposits increase, but also the adverse effect on wear increases. On the other hand, when the product exceeds 50000, the viscosity is too high, the fluidity is insufficient, and the deposit is increased.
- Mn number average molecular weight
- the fragility of the deposit is measured by the height of the product obtained by firing the cylinder lubricant composition with a TGA (Thermo Gravimetry Analyzer). Specifically, a cylinder lubricant composition is collected from a hermetic pan of a TGA (thermobalance), fired, and baked as shown in FIG. Measure the height. The higher this height, the easier it is to break if it is formed as a deposit. Details are described in the Examples column.
- the number average molecular weight (Mn) of the (B) ashless dispersant in the present invention is preferably 2500 or more, more preferably 3000 or more, further preferably 4000 or more, and most preferably 5000 or more, but 10,000 or less. Preferably there is.
- the number average molecular weight of the ashless dispersant is less than 2500, the deposit intended in the present invention is not easily broken, not only the deposits increase, but also the adverse effect on wear increases.
- the number average molecular weight of the ashless dispersant exceeds 10,000, the viscosity is too high, the fluidity becomes insufficient, and the deposit increases.
- the blending amount and effective concentration of (B) the ashless dispersant are not particularly limited as long as the product of the number average molecular weight (Mn) of the ashless dispersant, the blending amount and the effective concentration is 9000 or more.
- the effective concentration of (B) ashless dispersant ratio of the mass remaining in the rubber film to the amount of sample initially collected as a sample
- the concentration of the ash dispersant in the composition is preferably in the range of 0.9 to 14% by mass based on the total amount of the lubricating oil composition.
- the cylinder lubricating oil composition for a crosshead type diesel engine of the present invention contains (C) a metal-based detergent (hereinafter also referred to as (C) component) as an essential component.
- C a metal-based detergent
- any compound usually used for lubricating oils can be used, and examples thereof include sulfonate detergent, phenate detergent, salicylate detergent, and naphthenate detergent. . In use, these metal detergents can be used alone or in combination of two or more.
- Examples of the sulfonate detergent include alkali metal salts and alkaline earth metals of alkyl aromatic sulfonic acids obtained by sulfonating alkyl aromatic compounds having a weight average molecular weight of 400 to 1500, preferably 700 to 1300. A salt or a (over) basic salt thereof can be used.
- Examples of the alkali metal or alkaline earth metal include sodium, potassium, magnesium, barium, and calcium. Magnesium or calcium is preferable, and calcium is particularly preferable.
- Examples of the alkyl aromatic sulfonic acid include so-called petroleum sulfonic acid and synthetic sulfonic acid.
- Examples of the petroleum sulfonic acid herein include those obtained by sulfonating an alkyl aromatic compound of a lubricating oil fraction of mineral oil, and so-called mahoganic acid that is by-produced during white oil production.
- the synthetic sulfonic acid for example, an alkylbenzene having a linear or branched alkyl group, which is produced as a by-product from an alkylbenzene production plant that is a raw material of a detergent or obtained by alkylating a polyolefin with benzene, is used.
- a sulfonated one or a sulfonated alkylnaphthalene such as dinonylnaphthalene is used.
- the sulfonating agent for sulfonating these alkyl aromatic compounds is not particularly limited, but usually fuming sulfuric acid or sulfuric anhydride is used.
- the alkyl metal sulfide alkali metal salt, alkaline-earth metal salt, or its (over) basic salt which has a structure shown by following formula (5) can be used.
- the alkali metal or alkaline earth metal include sodium, potassium, magnesium, barium, and calcium. Magnesium or calcium is preferable, and calcium is particularly preferable.
- R 6 represents a linear or branched, saturated or unsaturated alkyl group or alkenyl group having 6 to 21 carbon atoms
- m is a degree of polymerization
- S is sulfur.
- x represents an integer of 1 to 3.
- the carbon number of the alkyl group and alkenyl group in Formula (5) is preferably 9-18, more preferably 9-15. If the carbon number is less than 6, the solubility in the base oil may be inferior. On the other hand, if the carbon number exceeds 21, the production is difficult and the heat resistance may be inferior.
- phenate metal detergents those containing an alkylphenol sulfide metal salt having a polymerization degree m of 4 or more, particularly m of 4 to 5 shown in the formula (5) are preferable because of excellent heat resistance.
- Examples of the salicylate-based detergent include alkali metal, alkaline earth metal salicylate having one hydrocarbon group having 1 to 19 carbon atoms or (over) basic salt thereof, and hydrocarbon group having 20 to 40 carbon atoms.
- These hydrocarbon groups may be the same or different.
- Examples of the alkali metal or alkaline earth metal include sodium, potassium, magnesium, barium, and calcium. Magnesium and / or calcium are preferable, and calcium is particularly preferably used.
- the base number of component (C) is preferably in the range of 50 to 500 mgKOH / g, more preferably in the range of 100 to 450 mgKOH / g, and still more preferably in the range of 120 to 400 mgKOH / g.
- the base number is less than 50 mgKOH / g, the corrosion wear may increase.
- it exceeds 500 mgKOH / g there may be a problem in solubility.
- the metal ratio of the component (C) is not particularly limited, but the lower limit is preferably 1 or more, more preferably 2 or more, particularly preferably 2.5 or more, and the upper limit is preferably 20 or less, more preferably 19 or less, particularly preferably. Is preferably 18 or less.
- the metal ratio here is represented by the valence of the metal element in the component (C) ⁇ metal element content (mol%) / soap group content (mol%).
- the metal element means calcium, magnesium and the like
- the soap group means a sulfonic acid group, a phenol group, a salicylic acid group and the like.
- the component (C) can be used alone, but it is preferable to use two or more kinds in combination.
- the component (C) can be used alone, but it is preferable to use two or more kinds in combination.
- overbased Ca phenate / overbased Ca sulfonate (2) overbased Ca phenate / overbased Ca salicylate, (3) overbased Ca phenate / overbased Ca sulfonate / A combination of overbased Ca salicylate is preferred.
- a preferred ratio of (1) overbased Ca phenate / overbased Ca sulfonate or (2) overbased Ca phenate / overbased Ca salicylate is 0.1 or more in terms of the weight ratio of the additive. 2 or more is more preferable, and 0.3 or more is most preferable. This is because the heat resistance is inferior when the ratio is less than 0.1.
- the ratio is preferably 9 or less, more preferably 7 or less, and most preferably 5 or less. This is because when the ratio exceeds 9, the height in the TGA firing test is not sufficient, and the deposit on the piston top land is not sufficiently reduced.
- overbased Ca phenate / overbased Ca sulfonate / overbased Ca salicylate the sum of the overbased Ca sulfonate and the overbased Ca salicylate with respect to the overbased Ca phenate is the above ratio. Is preferred.
- 0.1 or more are preferable, 0.2 or more are further more preferable, and 0.3 or more are the most preferable. This is because if the weight ratio is less than 0.1, the deposit may increase conversely in a state far exceeding 300 ° C.
- the weight ratio is preferably 9 or less, more preferably 7 or less, and most preferably 5 or less. When the weight ratio exceeds 9, the cleanliness deteriorates.
- the content ratio of the component (C) is preferably 3 to 30% by mass, more preferably 6 to 25% by mass, and particularly preferably 8 to 20% by mass based on the total amount of the composition. is there.
- the content ratio of the component (C) is less than 3% by mass, the required cleanliness and acid neutralization may not be obtained.
- the content exceeds 30% by mass the excess metal component is a piston. There is a risk of accumulation.
- the content of the metal component based on the component (C) is preferably 0.35 to 3.6% by mass, more preferably 1.0 to 2.9, based on the total amount of the composition.
- the mass is particularly preferably 1.4 to 2.7 mass%.
- the content ratio of the metal component based on the component (C) is less than 0.7% by mass, the necessary cleanliness and acid neutralization may not be obtained.
- the content exceeds 3.6% by mass In this case, excessive ash may accumulate on the piston top land, causing bore polishing or scuffing of the liner.
- the component (C) of the present invention needs to have an endothermic peak temperature measured by DSC (Differential scanning calorimeter) of 460 ° C. or lower.
- the DSC measurement conditions are as follows. Equipment: TA Instruments DSC2920 Sample collection bread: hermetic bread Sample collection amount: 30 mg Atmosphere: Nitrogen (Flow rate: 50 ml / min) Temperature increase rate: 50 ° C / min Endothermic peak temperature: endothermic peak temperature after the diluent oil of the additive has evaporated
- the lower limit of the endothermic peak temperature of (C) the metallic detergent is not particularly limited, but is preferably 350 ° C. or higher. Below this, the compound becomes unstable and the heat resistance may be insufficient.
- the lubricating oil composition of the present invention preferably contains a sulfur-based extreme pressure agent as the other component.
- a sulfur-based extreme pressure agent include dihydrocarbyl polysulfide, sulfurized fatty acid, sulfurized olefin, sulfurized ester, sulfurized fat, sulfurized mineral oil, thiazole compound, thiadiazole compound, and alkylthiocarbamate compound.
- the lubricating oil composition of the present invention preferably contains an organic molybdenum compound.
- the organic molybdenum compound include organic molybdenum compounds containing sulfur such as molybdenum dithiophosphate and molybdenum dithiocarbamate (MoDTC); molybdenum compounds (eg, molybdenum oxide such as molybdenum dioxide and molybdenum trioxide; orthomolybdic acid, para Molybdic acid such as molybdic acid and (poly) sulfurized molybdic acid; molybdate such as metal salt and ammonium salt of molybdic acid; molybdenum sulfide such as molybdenum disulfide, molybdenum trisulfide, molybdenum pentasulfide, and polysulfide molybdenum; Metal salts or amine salts of molybdic acid, sulfurized molybdic acid, molybdenum halides such as moly
- the lubricating oil composition of the present invention preferably contains zinc dithiophosphate (ZnDTP) (hereinafter sometimes referred to as component (E)) as an antiwear agent.
- ZnDTP zinc dithiophosphate
- the zinc dithiophosphate include 3 to 18 carbon atoms such as zinc dipropyldithiophosphate, zinc dibutyldithiophosphate, zinc dipentyldithiophosphate, zinc dihexyldithiophosphate, zinc diheptyldithiophosphate, or zinc dioctyldithiophosphate.
- a dialkyldithiophosphate zinc having a linear or branched (primary, secondary or tertiary, preferably primary or secondary) alkyl group having 3 to 10 carbon atoms
- the lubricating oil composition of the present invention is generally used in lubricating oils depending on its purpose in order to further improve its performance or to add other required performance in addition to the above components.
- Optional additives can be further included. Examples of such additives include antioxidants, ashless friction modifiers, corrosion inhibitors, rust inhibitors, demulsifiers, metal deactivators, antifoaming agents, and colorants.
- antioxidants examples include ashless antioxidants such as phenols and amines; and metal antioxidants such as copper and molybdenum.
- the ratio in the case of containing these is usually 0.1 to 5% by mass based on the total amount of the composition.
- Examples of the ashless friction modifier include fatty acid ester, aliphatic amine, and fatty acid amide.
- the ratio in the case of containing these is usually 0.1 to 5% by mass based on the total amount of the composition.
- corrosion inhibitor examples include benzotriazole, tolyltriazole, thiadiazole, and imidazole compounds.
- rust inhibitor examples include petroleum sulfonate, alkylbenzene sulfonate, dinonylnaphthalene sulfonate, alkenyl succinate, and polyhydric alcohol ester.
- demulsifier examples include polyalkylene glycol nonionic surfactants such as polyoxyethylene alkyl ether, polyoxyethylene alkyl phenyl ether, and polyoxyethylene alkyl naphthyl ether.
- metal deactivator examples include imidazoline, pyrimidine derivatives, alkylthiadiazole, mercaptobenzothiazole, benzotriazole or derivatives thereof, 1,3,4-thiadiazole polysulfide, 1,3,4-thiadiazolyl-2,5- Bisdialkyldithiocarbamate, 2- (alkyldithio) benzimidazole, or ⁇ - (o-carboxybenzylthio) propiononitrile.
- antifoaming agent examples include silicone oils and alkenyl succinic acid derivatives having a kinematic viscosity at 25 ° C. of less than 0.1 to 100 mm 2 / s.
- the content is usually 0.005 to 5% by mass based on the total amount of the composition, and usually 0.0005 to 1% by mass for the antifoaming agent. It is chosen from the range.
- the cylinder lubricating oil composition for a crosshead type diesel engine of the present invention preferably has a base number of 10 mgKOH / g or more, more preferably 20 mgKOH / g or more, still more preferably 25 mgKOH / g or more, particularly preferably 40 mgKOH. / G or more, preferably 100 mgKOH / g or less, more preferably 85 mgKOH / g or less, and even more preferably 75 mgKOH / g or less.
- the base number is less than 10 mgKOH / g, the piston cleanliness is insufficient.
- the base number exceeds 100 mgKOH / g, the excessive base number, that is, the metal carbonate forms a deposit and causes wear and piston ring sticking.
- the base number when using both high sulfur fuel and low sulfur fuel is preferably 50 mgKOH / g or more, more preferably 60 mgKOH / g or more, and still more preferably 70 mgKOH / g or more.
- the base number is less than 50 mgKOH / g, when high sulfur fuel is used, the neutralizing ability of the generated acidic substance is not sufficient, and corrosion wear cannot be suppressed.
- the upper limit in this case is as described above.
- the base number is preferably 60 mgKOH / g or less, more preferably 50 mgKOH / g or less, and still more preferably 45 mgKOH / g or less.
- the base number exceeds 60 mgKOH / g, when low-sulfur fuel or gas fuel is used, there is a high possibility that abrasion or piston ring sticking occurs due to the formation of an excess base number, that is, deposit due to metal carbonate.
- the lower limit in this case is as described above.
- the high sulfur fuel means a fuel containing 3.5% by mass or more of sulfur
- the low sulfur fuel means a fuel having a sulfur content of less than 1.0% by mass.
- a fuel having a sulfur content of 1.0% by mass or more and less than 3.5% by mass can be handled in either a high sulfur fuel or a low sulfur fuel.
- the sulfur content of gas is 0.1 mass% or less.
- Example 1 A lubricating oil composition having the formulation shown in Table 1 was prepared, and as described above, the fragility of the formed deposit was measured by TGA.
- the test conditions are as follows. Equipment: TA Instruments TGA2950 Sample collection bread: hermetic bread Sample collection amount: 30 mg Atmosphere: Nitrogen (Flow rate: 50 ml / min) Temperature increase rate: 50 ° C / min Deposit fragility: ash content height after holding from 30 ° C. after raising temperature from room temperature to 600 ° C.
- FIG. 1 shows an example.
- a WD300 engine test manufactured by Ricardo Co., Ltd. was performed on the prepared lubricating oil composition under the following conditions.
- Lubricating oil temperature 80 ° C
- Piston Topland Evaluation Method Merit score of the Petroleum Institute Method (JPI-5S-15) (The higher the score, the less the deposit)
- the base oil: base oil ratio was changed to 44 to 69 parts by mass of solvent refined base oil SAE30 and 31 to 56 parts by mass of bright stock, and the kinematic viscosity (100 ° C.) of the lubricating oil composition was 20.0 to 21.0 mm. adjusted to 2 / s * solvent refined base oil SAE 30: kinematic viscosity (40 °C) 94.33mm 2 / s , kinematic viscosity (100 °C) 10.79mm 2 / s ** Bright stock: kinematic viscosity (40 ° C.) 466.6 mm 2 / s, kinematic viscosity (100 ° C.) 31.57 mm 2 / s
- Metal detergent 1 Overbased calcium salicylate, base number 320 mgKOH / g, endothermic peak temperature in DSC 403 ° C.
- Metal detergent 2 Overbased calcium sulfonate, base number 400 mgKOH / g, endothermic peak temperature at DSC 449 ° C.
- Metal detergent 3 Overbased calcium sulfonate, base number 400 mgKOH / g, endothermic peak temperature in DSC 470 ° C.
- Metal detergent 4 Overbased calcium sulfonate, base number 400 mgKOH / g, endothermic peak temperature at DSC 481 ° C.
- Metal detergent 5 Overbased calcium sulfonate, base number 400 mgKOH / g, endothermic peak temperature in DSC 498 ° C.
- Metal detergent 6 Overbased calcium sulfonate, base number 400 mgKOH / g, endothermic peak temperature at DSC 512 ° C.
- Metal detergent 7 Overbased calcium phenate, base number 150 mgKOH / g, endothermic peak temperature at DSC 484 ° C.
- the height of the ash has a very good correlation with the piston top land score by the Ricardo WD300 engine test. That is, when the height of the ash exceeds 2 mm, the score of the deposit exceeds 3.5, which means that there is little adhesion of the deposit.
- the cylinder lubricating oil composition of the example has a high ash content and a high piston top land rating, whereas the product of the number average molecular weight, blending amount and effective concentration of the ashless dispersant is less than 9000.
- the cylinder lubricant compositions of Examples 2 to 4 and the cylinder lubricant compositions of Comparative Examples 5 to 8 that do not contain a metal detergent having an endothermic peak temperature of 460 ° C. or lower have a low ash content, and the piston top land The score of was also low.
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Abstract
Description
前記(B)無灰分散剤の数平均分子量と配合量と有効濃度の積が9000以上であり、
前記(C)金属系清浄剤は、DSCにより測定される昇温速度50℃/minにおける吸熱ピーク温度が460℃以下であることを特徴とするクロスヘッド型ディーゼル機関用シリンダー潤滑油組成物である。
(B−1)炭素数40~400のアルキル基又はアルケニル基を分子中に少なくとも1個有するコハク酸イミド、あるいはその誘導体、
(B−2)炭素数40~400のアルキル基又はアルケニル基を分子中に少なくとも1個有するベンジルアミン、あるいはその誘導体、
(B−3)炭素数40~400のアルキル基又はアルケニル基を分子中に少なくとも1個有するポリアミン、あるいはその誘導体。
R5−NH−(CH2CH2NH)k−H ・・・(4)
(i)ゴム膜内に試料約5gを採取。
(ii)ゴム膜を糸で縛り、円筒ろ紙の中にゴム膜を入れる。
(iii)円筒ろ紙を入れたソックスレー抽出器に入れる。
(iv)平フラスコに石油エーテルを100ml入れ、その上にソックスレー抽出器を取り付ける。
(v)平フラスコ部をウォーターバスで加温(70℃)し、ソックスレー抽出器は取り付けた冷却器で冷やす。
(vi)2日間加熱還流する。
(vii)ゴム膜内の透析残分をビーカーに移し、ゴム膜付着物を石油エーテルでビーカー内に洗い流す。石油エーテルをウォーターバスで加温し除去し、ゴム膜残分を求める。
(viii)平フラスコ部の透析分の石油エーテルをウォーターバスで加温し除去し、ゴム膜透析分を求める。
装置:Waters Alliance2695
カラム:東ソーGMHHR−M
移動相:テトラヒドロフラン
サンプルの溶媒希釈濃度:1質量%(溶媒はテトラヒドロフラン)
温度:23℃
流速:1ml/min
サンプル量:100μl
検出器:RI
分子量:ポリスチレン換算
装置:TAインスツルメントDSC2920
サンプル採取パン:ハーメチックパン
サンプル採取量:30mg
雰囲気:窒素(流量:50ml/min)
昇温速度:50℃/min
吸熱ピーク温度:添加剤の希釈油が蒸発した後の吸熱ピーク温度
表1に示す配合処方の潤滑油組成物を調製し、上述したように、形成されるデポジットの壊れ易さをTGAにより測定した。試験条件は下記の通りである。
装置:TAインスツルメントTGA2950
サンプル採取パン:ハーメチックパン
サンプル採取量:30mg
雰囲気:窒素(流量:50ml/min)
昇温速度:50℃/min
デポジットの壊れ易さ:室温から600℃まで昇温させ600℃到達後、30min保持後の灰分高さ
図1に例を示す。
装置:リカルド社製WD300エンジン(気筒数:1、排気量:2.2L、ピストンボア:135mm)
軸平均有効圧力:20bar
回転数:1200rpm
燃料:軽油(硫黄分10ppm未満)
冷却水出口温度:85℃
潤滑油温度:80℃
ピストントップランド評価法:石油学会法(JPI−5S−15)のメリット評点(評点が高い程、堆積が少ないことを示す)
* 溶剤精製基油SAE30:動粘度(40℃)94.33mm2/s、動粘度(100℃)10.79mm2/s
** ブライトストック:動粘度(40℃)466.6mm2/s、動粘度(100℃)31.57mm2/s
無灰分散剤2:ポリブテニルコハク酸イミド、Mn2660(有効濃度50質量%、採取したサンプル量に対するゴム膜内に残った質量の比=0.5)、DSCでの吸熱ピーク温度447℃
無灰分散剤3:ポリブテニルコハク酸イミド、Mn3180(有効濃度60質量%、採取したサンプル量に対するゴム膜内に残った質量の比=0.6)、DSCでの吸熱ピーク温度456℃
無灰分散剤4:ポリブテニルコハク酸イミド、Mn4460(有効濃度50質量%、採取したサンプル量に対するゴム膜内に残った質量の比=0.5)、DSCでの吸熱ピーク温度442℃
無灰分散剤5:ポリブテニルコハク酸イミド、Mn4770(有効濃度60質量%、採取したサンプル量に対するゴム膜内に残った質量の比=0.6)、DSCでの吸熱ピーク温度450℃
無灰分散剤6:ポリブテニルコハク酸イミド、Mn7630(有効濃度45質量%、採取したサンプル量に対するゴム膜内に残った質量の比=0.45)、DSCでの吸熱ピーク温度453℃
金属系清浄剤2:過塩基性カルシウムスルホネート、塩基価400mgKOH/g、DSCでの吸熱ピーク温度449℃
金属系清浄剤3:過塩基性カルシウムスルホネート、塩基価400mgKOH/g、DSCでの吸熱ピーク温度470℃
金属系清浄剤4:過塩基性カルシウムスルホネート、塩基価400mgKOH/g、DSCでの吸熱ピーク温度481℃
金属系清浄剤5:過塩基性カルシウムスルホネート、塩基価400mgKOH/g、DSCでの吸熱ピーク温度498℃
金属系清浄剤6:過塩基性カルシウムスルホネート、塩基価400mgKOH/g、DSCでの吸熱ピーク温度512℃
金属系清浄剤7:過塩基性カルシウムフェネート、塩基価150mgKOH/g、DSCでの吸熱ピーク温度484℃
Claims (2)
- (A)潤滑油基油に(B)無灰分散剤と(C)金属系清浄剤を含有し、
前記(B)無灰分散剤の数平均分子量と配合量と有効濃度の積が9000以上であり、
前記(C)金属系清浄剤は、DSCにより測定される昇温速度50℃/minにおける吸熱ピーク温度が460℃以下である
ことを特徴とするクロスヘッド型ディーゼル機関用シリンダー潤滑油組成物。 - 前記(B)無灰分散剤は、数平均分子量が2500以上であることを特徴とする請求項1に記載のクロスヘッド型ディーゼル機関用シリンダー潤滑油組成物。
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US14/347,816 US20140378356A1 (en) | 2011-09-30 | 2012-03-08 | Cylinder lubricating oil composition for crosshead diesel engine |
CN201280048231.9A CN103958654B (zh) | 2011-09-30 | 2012-03-08 | 十字头型柴油机用气缸润滑油组成物 |
KR1020147011494A KR101890605B1 (ko) | 2011-09-30 | 2012-03-08 | 크로스헤드형 디젤 기관용 실린더 윤활유 조성물 |
SG11201401057TA SG11201401057TA (en) | 2011-09-30 | 2012-03-08 | Cylinder lubricating oil composition for crosshead diesel engine |
EP12834993.3A EP2762555A4 (en) | 2011-09-30 | 2012-03-08 | LUBRICANT COMPOSITION FOR CYLINDERS FOR A DIESEL ENGINE WITH HOUSING |
JP2013535954A JP5913338B2 (ja) | 2011-09-30 | 2012-03-08 | クロスヘッド型ディーゼル機関用シリンダー潤滑油組成物 |
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PCT/JP2012/056610 WO2013046755A1 (ja) | 2011-09-30 | 2012-03-08 | クロスヘッド型ディーゼル機関用シリンダー潤滑油組成物 |
Country Status (7)
Country | Link |
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US (1) | US20140378356A1 (ja) |
EP (1) | EP2762555A4 (ja) |
JP (1) | JP5913338B2 (ja) |
KR (1) | KR101890605B1 (ja) |
CN (1) | CN103958654B (ja) |
SG (1) | SG11201401057TA (ja) |
WO (1) | WO2013046755A1 (ja) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013253243A (ja) * | 2012-06-07 | 2013-12-19 | Infineum Internatl Ltd | 船舶用エンジンの潤滑 |
US10982168B2 (en) | 2015-09-28 | 2021-04-20 | Eneos Corporation | Cylinder lubricating oil composition for crosshead diesel engine |
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- 2012-03-08 JP JP2013535954A patent/JP5913338B2/ja active Active
- 2012-03-08 KR KR1020147011494A patent/KR101890605B1/ko active IP Right Grant
- 2012-03-08 SG SG11201401057TA patent/SG11201401057TA/en unknown
- 2012-03-08 US US14/347,816 patent/US20140378356A1/en not_active Abandoned
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Cited By (2)
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JP2013253243A (ja) * | 2012-06-07 | 2013-12-19 | Infineum Internatl Ltd | 船舶用エンジンの潤滑 |
US10982168B2 (en) | 2015-09-28 | 2021-04-20 | Eneos Corporation | Cylinder lubricating oil composition for crosshead diesel engine |
Also Published As
Publication number | Publication date |
---|---|
KR20140082992A (ko) | 2014-07-03 |
KR101890605B1 (ko) | 2018-08-22 |
EP2762555A1 (en) | 2014-08-06 |
CN103958654B (zh) | 2016-02-10 |
JPWO2013046755A1 (ja) | 2015-03-26 |
JP5913338B2 (ja) | 2016-04-27 |
US20140378356A1 (en) | 2014-12-25 |
CN103958654A (zh) | 2014-07-30 |
EP2762555A4 (en) | 2015-06-17 |
SG11201401057TA (en) | 2014-11-27 |
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