EP0273588B1 - Alkylphénates de métaux alcalino-terreux sulfurés, leur préparation et leur utilisation - Google Patents

Alkylphénates de métaux alcalino-terreux sulfurés, leur préparation et leur utilisation Download PDF

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Publication number
EP0273588B1
EP0273588B1 EP87310461A EP87310461A EP0273588B1 EP 0273588 B1 EP0273588 B1 EP 0273588B1 EP 87310461 A EP87310461 A EP 87310461A EP 87310461 A EP87310461 A EP 87310461A EP 0273588 B1 EP0273588 B1 EP 0273588B1
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Prior art keywords
process according
concentrate
lubricating oil
alkaline earth
earth metal
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EP0273588B2 (fr
EP0273588A1 (fr
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Charles Cane
John Crawford
Sean Patrick O'connor
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Lubrizol Adibis Holdings UK Ltd
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BP Chemicals Additives Ltd
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    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
    • C10M159/12—Reaction products
    • C10M159/20—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products
    • C10M159/22—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products containing phenol radicals

Definitions

  • the present invention relates in general to the production of sulphurised alkaline earth metal hydrocarbyl phenate additive concentrates and to their use as lubricating oil additives.
  • the present invention relates to the production of sulphurised alkaline earth metal hydrocarbyl phenate-containing additive concentrates having a high total base number (TBN) and an acceptable viscosity from sulphurised alkaline earth metal hydrocarbyl phenates having lower TBNs.
  • TBN total base number
  • One class of compounds generally employed to neutralise the acidic materials and disperse sludge within the lubricating oil are the sulphurised metal alkyl phenates, wherein the metal is an alkaline earth metal such as calcium, magnesium or barium. Both “normal” and “overbased” sulphurised alkaline earth metal alkyl phenates have been employed.
  • the term “overbased” is used to describe those sulphurised alkaline earth metal alkyl phenates in which the ratio of the number of equivalents of the alkaline earth metal moiety to the number of equivalents of the phenol moiety is greater than one, and is usually greater than 1.2 and may be as high as 4.5 or greater.
  • the equivalent ratio of alkaline earth metal moiety to phenol moiety in "normal” alkaline earth metal alkyl phenates is one.
  • the "overbased” material contains greater than 20% in excess of the alkaline earth metal present in the corresponding "normal” material. For this reason "overbased” sulphurised alkaline earth metal alkyl phenates have a greater capability for neutralising acidic matter than do the corresponding "normal” alkaline earth metal alkyl phenates.
  • the prior art teaches many methods for preparing both "normal” and “overbased” sulphurised metal alkyl phenates.
  • One such method for preparing "overbased” sulphurised alkyl phenates generally referred to as the “single lime addition” process comprises reacting an alkyl phenol, in the presence of lubricating oil, sulphur, a hydroxylic compound and excess alkaline earth metal hydroxide (above the stoichiometric proportion required to neutralise the alkyl phenol), to form an intermediate product, followed by carbonation, a heading distillation (to remove unreacted hydroxylic compound) and filtration.
  • intermediate product is accompanied by a marked increase in viscosity while the subsequent carbonation reduces the viscosity to a relatively low level.
  • the increase in viscosity accompanying the formation of the intermediate product is undesirable because the reaction mixture becomes difficult to agitate to the detriment of subsequent reactions. Whilst this increase in viscosity may be controlled to an acceptable level by incorporation of less alkaline earth metal hydroxide in the reaction, the overbased alkyl phenate product necessarily possesses a reduced neutralisation capacity.
  • the alkaline earth metal hydroxide may be added in two, (generally referred to as the "double lime addition” process) or three separate reaction steps, with sequential carbonation steps.
  • this method involves relatively long batch times.
  • viscosity depressants such as tridecanol, 2-ethylhexanol, or similar boiling range hydroxylic solvent, in the production of the intermediate product but such an expedient increases the raw material cost of the process.
  • TBN total base number
  • compositions having a TBN in excess of 300 and in some cases greater than 350 whilst retaining an acceptable viscosity, that is a viscosity of less than 1000 cSt, and avoiding insolubility by incorporating into a reaction mixture containing a sulphurised alkaline earth metal alkyl phenate at least one carboxylic acid or acid derivative thereof having at least 10 carbon atoms in the molecule.
  • US-A-4049560 describes the production of an overbased magnesium detergent by a process in which carbon dioxide is introduced into a reaction mixture which comprises:
  • the amount of carboxylic acid (component (e)) is preferably in the range 0.5 to 2.0% by weight.
  • the product prepared by this reaction is said to have a TBN of about 200 to 250, e.g. about 225.
  • EP-A-0094814 discloses an additive concentrate for incorporation in a lubricating oil composition
  • a lubricating oil composition comprising lubricating oil, and from 10 to 90 wt % of an overbased alkaline earth metal hydrocarbyl sulphurised phenate which has been treated, either during or subsequent to the overbasing process, with from 0.1 to 10, preferably 2 to 6, wt % (based on the weight of additive concentrate) of an acid of the formula: (wherein R is a C10 to C 24 unbranched alkyl or alkenyl group, and R 1 is hydrogen, a C 1 to C 4 alkyl group or a -CH 2 -COOH group) or an anhydride or a salt thereof.
  • the object of the invention of EP-A-0094814 is to overcome problems encountered with many additive concentrates containing overbased additives, namely lack of stability giving rise to sedimentation and foaming problems.
  • the problem of EP-A-0094814 is not that of producing phenates having a TBN of greater than 300 and indeed the phenates produced by the process of the invention, although overcoming the problems of stability and foaming, have TBN values of less than 300.
  • Our European Application Publication No. 0095322 discloses a process for the production of either an alkaline earth metal alkyl phenate or a sulphurised alkaline earth metal alkyl phenate which process comprises reacting at elevated temperature, in the presence or absence of sulphur, an alkyl phenol with an alkaline earth metal base in the presence as solvent of either an alkylene glycol alkyl ether or a polyalkylene glycol alkyl ether of formula: wherein R is a C 1 to C 6 alkyl group, R 1 is alkylene, R 2 is hydrogen or C 1 to C 6 alkyl and x is an integer in the range 1 to 6 and as catalyst an inorganic halide.
  • a small amount suitably up to 2% w/w of an acid, a suitable acid being stearic acid.
  • stearic acid to the reactants can, it is said, enhance the ability of alkylphenates to minimise emulsion formation in water.
  • the present invention provides a process for the production of an additive concentrate suitable for incorporation into a finished lubricating oil composition, the additive concentrate comprising:
  • the process of the invention is advantageous because it affords a method for up-grading low TBN products of the prior art or off-specification products into high TBN products having an acceptable viscosity. Moreover, because hydrogen sulphide is not evolved during operation of the process of the invention, in contrast to processes for producing sulphurised alkaline earth metal alkyl phenates involving the reaction of an alkyl phenol and sulphur, by the more conventional routes, the hydrogen sulphide disposal problem is avoided, thereby allowing manufacture in environmentally sensitive locations and the use of less sophisticated plant.
  • Component (a) of the concentrate is a lubricating oil.
  • the lubricating oil may suitably be either an animal oil, a vegetable oil or a mineral oil.
  • the lubricating oil may be a petroleum-derived lubricating oil, such as a naphthenic base, paraffin base or mixed base oil. Solvent neutral oils are particularly suitable.
  • the lubricating oil may be a synthetic lubricating oil.
  • Suitable synthetic lubricating oils include synthetic ester lubricating oils, which oils include diesters such as di-octyl adipate, di-octyl sebacate and tridecyladipate, or polymeric hydrocarbon lubricating oils, for example liquid polyisobutenes and poly-alpha olefins.
  • the lubricating oil may suitably comprise from 10 to 90%, preferably from 10 to 70%, by weight of the concentrate.
  • Component (b) is a lubricating oil soluble sulphurised alkaline earth metal hydrocarbyl phenate modified by incorporation of from greater than 2 to 35% by weight based on the weight of the concentrate of either (i) or (ii).
  • the alkaline earth metal may be strontium, calcium, magnesium or barium, preferably calcium, barium or magnesium, more preferably calcium.
  • the hydrocarbyl phenate moiety of the sulphurised alkaline earth metal hydrocarbyl phenate is preferably derived from at least one alkyl phenol.
  • the alkyl groups of the alkyl phenol may be branched or unbranched. Suitable alkyl groups contain from 4 to 50, preferably from 9 to 28 carbon atoms.
  • a particularly suitable alkyl phenol is the C12-alkyl phenol obtained by alkylating phenol with propylene tetramer.
  • the sulphurised alkaline earth metal hydrocarbyl phenate is modified by incorporation of either (i) or (ii).
  • this is at least one carboxylic acid having the formula (I) or an acid anhydride or ester thereof.
  • R in the formula (I) is an unbranched alkyl or alkenyl group.
  • Preferred acids of formula (I) are those wherein R is a C 10 to C 24 , more preferably C 18 to C 24 straight chain alkyl groups and R 1 is hydrogen.
  • suitable saturated carboxylic acids of formula (I) include capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, arachidic acid, behenic acid and lignoceric acid.
  • suitable unsaturated acids of formula (I) include lauroleic acid, myristoleic acids, palmitoleic acid, oleic acid, gadoleic acid, erucic acid, ricinoleic acid, linoleic acid and linolenic acid.
  • Mixtures of acids may also be employed, for example rape top fatty acids.
  • Particularly suitable mixtures of acids are those commercial grades containing a range of acids, including both saturated and unsaturated acids.
  • Such mixtures may be obtained synthetically or may be derived from natural products, for example cotton oil, ground nut oil, coconut oil, linseed oil, palm kernel oil, olive oil, corn oil, palm oil, castor oil, soyabean oil, sunflower oil, herring oil, sardine oil and tallow.
  • Sulphurised acids and acid mixtures may also be employed.
  • the carboxylic acid there may be used the acid anhydride or the ester derivatives of the acid, preferably the acid anhydride. It is preferred however to use a carboxylic acid or mixture of carboxylic acids.
  • a preferred carboxylic acid of formula (I) is stearic acid.
  • the sulphurised alkaline earth metal hydrocarbyl phenate may be modified by incorporation of (ii), which is a di-or polycarboxylic acid containing from 36 to 100 carbon atoms or an acid anhydride or ester derivative thereof, preferably an acid anhydride thereof.
  • (ii) is a polyisobutene succinic acid or a polyisobutene succinic anhydride thereof.
  • the carboxylic acid(s) having the formula (I), the di-or polycarboxylic acid, or the acid anhydride or ester thereof is incorporated in an amount from greater than 10% to 35%, more preferably from 12 to 20%, for example about 16% by weight based on the weight of the concentrate.
  • An advantage of incorporating greater than 10% of the carboxylic acid or derivative thereof is generally relatively lower concentrate viscosity.
  • the alkaline earth metal may be present in the composition in an amount in the range from 10 to 20% by weight based on the weight of the concentrate.
  • sulphur may be present in the concentrate in an amount in the range from 1 to 6, preferably from 1.5 to 3% by weight based on the weight of the concentrate.
  • carbon dioxide may be present in the concentrate in an amount in the range from 5 to 20, preferably from 9 to 15% by weight based on the weight of the concentrate.
  • the TBN of the concentrate is greater than 350, more preferably greater than 400.
  • the concentrate may have a viscosity measured at 100°C of less than 1000 cSt, preferably less than 750 cSt, more preferably less than 500 cSt.
  • Component (A) of the reaction mixture is a sulphurised alkaline earth metal hydrocarbyl phenate having a TBN lower than that of the final product i.e. generally less than 300.
  • Any sulphurised alkaline earth metal hydrocarbyl phenate may be employed.
  • the sulphurised alkaline earth metal hydrocarbyl phenate may be carbonated or non-carbonated.
  • the alkaline earth metal moiety and the hydrocarbyl phenate moiety of the sulphurised alkaline earth metal hydrocarbyl phenate may suitably be as hereinbefore described.
  • Methods for preparing sulphurised alkaline earth metal hydrocarbyl phenates are well known in the art.
  • the precursors of a sulphurised alkaline earth metal hydrocarbyl phenate in the form of a non-sulphurised alkaline earth metal hydrocarbyl phenate may be employed.
  • the alkaline earth metal base (component B) may suitably be an alkaline earth metal oxide or hydroxide, preferably the hydroxide.
  • Calcium hydroxide may be added for example in the form of slaked lime.
  • Preferred alkaline earth metals are calcium, magnesium and barium and more preferred is calcium.
  • the alkaline earth metal base must be added in an amount relative to component (A) sufficient to produce a product having a TBN in excess of 300, preferably in excess of 350. This amount will depend on a number of factors including the nature of the sulphurised alkaline earth metal hydrocarbyl phenate.
  • the weight ratio of component (B) to component (A) may suitably be in the range from 0.1 to 50, preferably from 0.2 to 5.
  • the alkaline earth metal base (B) may be added in whole to the initial reactants, or in part to the initial reactants and the remainder in one or more portions at a subsequent stage or stages in the process.
  • component (B) is added in a single addition to the initial reactants.
  • Component (C) is either a polyhydric alcohol having from 2 to 4 carbon atoms, a di-or tri-(C 2 to C 4 ) glycol, an alkylene glycol alkyl ether or a polyalkylene glycol alkyl ether.
  • the polyhydric alcohol may suitably be either a dihydric alcohol, for example ethylene glycol or propylene glycol, or a trihydric alcohol, for example glycerol.
  • the di-or tri-(C 2 to C 4 ) glycol may suitably be either diethylene glycol or triethylene glycol.
  • the alkylene glycol alkyl ether or polyalkylene glycol alkyl ether may suitably be of the formula:- wherein R is a C 1 to C 6 alkyl group, R 1 is an alkylene group, R 2 is hydrogen or C 1 to C 6 alkyl and x is an integer in the range from 1 to 6.
  • Suitable solvents having the formula (II) include the monomethyl or dimethyl ethers of ethylene glycol, diethylene glycol, triethylene glycol or tetraethylene glycol.
  • a particularly suitable solvent is methyl digol (CH 3 0CH 2 CH 2 0CH 2 CH 2 0H). Mixtures of glycols and glycol ethers of formula (II) may also be employed.
  • glycol or glycol ether of formula (II) as solvent it is preferred to use in combination therewith an inorganic halide, for example ammonium chloride, and a lower, i.e. C 1 to C 4 , carboxylic acid, for example acetic acid.
  • an inorganic halide for example ammonium chloride
  • a lower, i.e. C 1 to C 4 carboxylic acid, for example acetic acid.
  • carboxylic acid for example acetic acid.
  • component (C) is either ethylene glycol or methyl digol, the latter in combination with ammonium chloride and acetic acid.
  • Component (D) is a lubricating oil as hereinbefore described with reference to the concentrate composition.
  • Component (E) is carbon dioxide, which may be added in the form of a gas or solid, preferably in the form of a gas. In gaseous form it may suitably be blown through the reaction mixture.
  • component (F) The carbon dioxide is preferably added subsequent to a single addition of component (B) at the conclusion of the reaction between component (A), (B), (C), (D) and (F).
  • Component (F) is either a carboxylic acid of formula (I), a di-or polycarboxylic acid containing from 36 to 100 carbon atoms, or an acid anhydride or ester thereof as hereinbefore described with reference to the concentrate composition.
  • the amount of the aforesaid required to provide from greater than 2 to 35% by weight based on the weight of the concentrate will be to a first approximation the amount defined in the concentrate. In calculating this amount allowance should be made for loss of water from carboxylic acids, for example.
  • the reaction may be performed in the presence of a diluent.
  • Suitable diluents are liquids having a volatility consistent with operation of the process, i.e. having a volatility such that they are readily strippable from the reaction mixture at the conclusion of the reaction.
  • suitable diluents include 2-ethyl hexanol, iso-octanol, iso-heptanol and tri-decanol.
  • sulphur that is sulphur additional to that already present by way of component (A)
  • sulphur addition leads to the evolution of hydrogen sulphide, thereby to some extent detracting from the advantage of the invention as hereinbefore mentioned.
  • the reaction is carried out in the presence of a further component which is a catalyst for the reaction.
  • a catalyst for the reaction there may be used an inorganic halide which may suitably be either a hydrogen halide, an ammonium halide or a metal halide.
  • the metal moiety of the metal halide may be zinc, aluminium or an alkaline earth metal, preferably calcium.
  • the chloride is preferred.
  • Suitable catalysts include hydrogen chloride, calcium chloride, ammonium chloride, aluminium chloride and zinc chloride, preferably calcium chloride.
  • the amount of catalyst employed may be up to 2.0% wt/wt.
  • reaction of components (A) - (F) and also the carbonation reaction may be carried out at elevated temperatures in the range from 120 to 200, preferably from about 130 to 165°C, though the actual temperature chosen for the reaction of components (A) - (F) and the carbonation may differ if desired.
  • the pressure may be atmospheric, subatmospheric or superatmospheric.
  • the concentrate may be recovered by conventional means, for example by distillative stripping of component (C) and diluent (if any).
  • the process of the invention will produce a concentrate having an acceptable viscosity, that is a viscosity of less than 1000 cSt at 100°C and can produce concentrates having a viscosity less than 750 or 500 cSt at 100°C.
  • the concentrates generally have desirable viscosity index properties. Such viscometric properties are advantageous because they facilitate processing (including filtration) of the concentrate.
  • the concentrate may be diluted with lubricating oil and still retain a TBN in excess of 300, particularly if the TBN of the concentrate as produced is high, for example above 400.
  • the present invention provides an additive concentrate suitable for incorporation into a finished lubricating oil which concentrate is obtainable by reacting at elevated temperature (A) a sulphurised alkaline earth metal hydrocarbyl phenate having a TBN less than that of the final additive concentrate, (B) an alkaline earth metal base either added in whole to the initial reactants, or in part to the initial reactants and the remainder in one or more portions at a subsequent stage or stages in the process, (C) either a polyhydric alcohol having from 2 to 4 carbon atoms, a di-or tri-(C 2 to C 4 ) glycol, an alkylene glycol alkyl ether or a polyalkylene glycol alkyl ether, (D) a lubricating oil, (E) carbon dioxide added subsequent to the, or each, addition of component (B), and (F) sufficient to provide from greater than 2 to 35% by weight based on the weight of the concentrate of either (i) a carboxylic acid having the formula (I) or
  • the present invention provides a finished lubricating oil composition which composition comprises a lubricating oil and sufficient of the additive concentrate produced in the manner as hereinbefore described to provide a TBN in the range from 0.5 to 120.
  • the finished lubricating oil composition contains sufficient of the concentrate to provide a TBN in the range from 0.5 to 100.
  • the amount of the concentrate present in the finished lubricating oil will depend on the nature of the final use. Thus, for marine lubricating oils the amount of concentrate composition present may suitably be sufficient to provide a TBN in the range from 9 to 100 and for automobile engine lubricating oils the amount may suitably be sufficient to provide a TBN in the range from 4 to 20.
  • the finished lubricating oil may also contain effective amounts of one or more other types of conventional lubricating oil additives, for example viscosity index improvers, anti-wear agents, antioxidants, dispersants, rust inhibitors, pour-point depressants, or the like, which may be incorporated into the finished lubricating oil composition either directly or through the intermediacy of the concentrate.
  • viscosity index improvers for example viscosity index improvers, anti-wear agents, antioxidants, dispersants, rust inhibitors, pour-point depressants, or the like, which may be incorporated into the finished lubricating oil composition either directly or through the intermediacy of the concentrate.
  • the concentrates of the present invention may also find application as fuels additives.
  • TBN is the Total Base Number in mg KOH/g as measured by the method of ASTM D2896.
  • a commercially available sulphurised calcium alkyl phenate derived from a C 12 -alkyl phenol was employed.
  • the phenate is supplied as a solution in lubricating oil, which forms from 36-40% w/w of the composition.
  • the composition has a TBN of 250 and a composition as follows:- calcium (9.25% w/w), sulphur (3.25% w/w) and carbon dioxide (4.6% w/w).
  • the "Charge" for any Example includes lubricating oil, this is additional to that already present in the phenate composition.
  • the viscosity was measured by the method of ASTM D445.
  • the charge was heated to 145-165 °C/700 mm Hg whilst adding 36 g ethylene glycol. It was then maintained for one hour at 165 °C/700 mg Hg. Carbon dioxide (50 g) was added at 165°C over 1 hour. The product was cooled to 125°C/700 mm Hg. Lime (33 g) was added. The temperature was raised to 165 °C/700 mm Hg and held at this temperature for one hour. Carbon dioxide (25 g) was added at 165°C over one hour. The product was then stripped at 200°C/10 0 mm Hg. Finally the product was filtered. It was observed that the filtration rate was very fast. 437 g product and 167 g distillate were obtained.
  • the product was analysed for calcium, sulphur and carbon dioxide. Its TBN, BPHVI50 and Viscosity at 100°C were determined. The BPHVI50 determination is a solubility test. Results of the test are expressed on the scale 1 (highly soluble; pass), 2 (borderline) and 3 (fail).
  • This Example demonstrates that a low TBN product can be converted to a high TBN product having an acceptable viscosity by the process of the invention.
  • the filtration rate was fast.
  • Example 2 As for Example 2 except that the temperature was 145 °C instead of 165°C in steps (d), (e) and (f).
  • Example 2 As for Example 2 except that the temperature was 130°C instead of 165°C in steps (d), (e) and (f).
  • Example 3 Charge: As for Example 3 except that calcium chloride was omitted.
  • the filtration step (h) was very difficult.
  • Example 3 demonstrates the desirability of using a catalyst in the process of the invention. In the absence of catalyst, although a lower V 100 was obtained, this was achieved at the expense of reduced incorporation of calcium and carbon dioxide, and moreover filtration was difficult.
  • Example 6 As for Example 6 except that the phenate was increased from 250 g to 268 g and the stearic acid was increased from 40 g to 51 g.
  • This Example demonstrates that it is possible to produce a high TBN concentrate having a low viscosity at a stearic acid content of 24.9% w/w.
  • step (h) The filtration rate in step (h) was slow.
  • Example 3 As for Example 3 except that the ethylene glycol addition in step (d) was reduced from 32 g to 16 g.
  • step (h) The filtration rate in step (h) was slow.
  • step (b) instead of 2-ethyl hexanol (190 g) there was added methyl diglycol (130 g) and in step (d) the addition of ethylene glycol was omitted.
  • step (h) The filtration rate in step (h) was rapid.
  • step (d) the pressure was 270 mm Hg.
  • Example 3 As for Example 3 except that instead of 190 g 2-ethyl hexanol there was used 40 g.
  • step (i) The filtration rate in step (i) was rapid.
  • This Example demonstrates that a lubricating oil can be replaced by a long carbon chain alpha-olefin (in this case C 18 .
  • This Example demonstrates that sulphurised calcium alkyl phenates derived from a mixture of C12/C22/C24 alkyl phenols can be upgraded.
  • Rape Top Fatty Acid can be used in the process of the invention.
  • step (a) instead of stearic acid (63 g) there was used Tall Oil Fatty Acid (63 g).
  • PIBSA polyisobutene succinic anhydride
  • Example 16 As for Example 16 except that instead of Tall Oil Fatty Acid (63 g) there was used behenic acid (63 g).
  • This Test is not an example according to the present invention and is included only for the purpose of demonstrating that lower carboxylic acids, in this case acetic acid, can not be used in the process of the invention.
  • Example 16 As for Example 16 except that instead of the commercially available sulphurised calcium alkyl phenate there was used an uncarbonated commercially available sulphurised calcium C 12 -alkyl phenate (145 TBN).
  • step (c) the amount of lime was increased from 66 g to 83 g and in step (f) the amount of carbon dioxide was increased from 66 g to 83 g.
  • This Example demonstrates that an uncarbonated sulphurised calcium alkyl phenate of low initial TBN can be used in the process of the invention.
  • This Example demonstrates that a low (150) TBN sulphurised calcium alkyl phenate can be upgraded to a high TBN product.
  • Example 14 As for Example 14 except that instead of the sulphurised calcium alkyl phenate derived from a mixture of alkyl phenols there was used the commercially available sulphurised calcium alkyl phenate derived from a C 12 -alkyl phenol (250 TBN).
  • step (b) instead of 2-ethyl hexanol (194 g) there was used iso-heptanol (190 g) and in step (d) the ethylene glycol was added quickly (within 1 minute).
  • the filtration rate was rapid.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)

Claims (32)

1. Procédé de production d'un concentré d'additif convenant pour être incorporé dans une composition d'huile lubrifiante formant un produit fini, ce concentré d'additif comprenant :
(a) une huile lubrifiante,
(b) un phénate de métal alcalino-terreux, hydrocarboné et sulfuré, soluble dans l'huile lubrifiante, qui a été modifié par incorporation d'une proportion, allant d'une valeur supérieure à 2 à 35 % en poids, rapporté au poids du concentré, soit
(i) d'au moins un acide carboxylique de formule :
Figure imgb0066
dans laquelle R est un radical alcoyle ou alcényle en C1 à à C24 et R1 est l'hydrogène, un radical alcoyle en Ci à C4 ou un radical -CH2-COOH, ou d'un anhydride ou un ester d'un tel acide, soit (ii) d'un acide dicarboxylique ou polycarboxylique contenant de 36 à 100 atomes de carbone, ou d'un anhydride ou un ester d'un tel acide, ce concentré ayant un IAT supérieur à 300 et une viscosité à 100 ° C inférieure à 1000 mm2.s-1 (cSt), ce procédé consistant à faire réagir, à température élevée :
(A) un phénate de métal alcalino-terreux, hydrocarboné et sulfuré, ayant un IAT inférieur à celui du concentré d'additif final,
(B) une base de métal alcalino-terreux ajoutée soit en totalité aux produits réagissants initiaux, soit en partie à ces produits réagissants initiaux et le reste en une ou plusieurs portions à un stade ou des stades ultérieurs au cours du procédé,
(C) un alcool polyhydrique ayant de 2 à 4 atomes de carbone, un diglycol ou triglycol en C2 à C4, un alcoyléther d'alcoylèneglycol ou un alcoyléther de polyalcoylèneglycol,
(D) une huile lubrifiante,
(E) du bioxyde de carbone ajouté à la suite de l'addition, ou de chaque addition, de composant
(B) et
(F) suffisamment, pour donner une proportion allant d'une valeur supérieure à 2 à 35 % en poids, rapporté au poids de concentré, soit (i) d'au moins un acide carboxylique de formule :
Figure imgb0067
dans laquelle R est un radical alcoyle ou alcényle en C1 à à C24 et R1 est l'hydrogène, un radical alcoyle en Ci à C4 ou un radical -CH2-COOH, ou d'un anhydride ou un ester d'un tel acide, soit (ii) d'un acide dicarboxylique ou polycarboxylique contenant de 36 à 100 atomes de carbone, ou d'un anhydride ou un ester d'un tel acide,
les rapports en poids des composants (A) à (F) étant tels qu'ils produisent un concentré ayant un IAT supérieur à 300.
2. Procédé suivant la revendication 1, selon lequel l'huile lubrifiante comprend de 10 à 90 % en poids du concentré.
3. Procédé suivant l'une des revendications 1 ou 2, selon lequel le métal alcalino-terreux du phénate de métal alcalino-terreux, hydrocarboné et sulfuré, soluble dans l'huile lubrifiante est le calcium, le magnésium ou le baryum.
4. Procédé suivant la revendication 3, selon lequel le métal alcalino-terreux est le calcium.
5. Procédé suivant l'une quelconque des revendications précédentes, selon lequel la partie phénate hydrocarboné du phénate de métal alcalino-terreux, hydrocarboné et sulfuré, soluble dans l'huile provient d'au moins un alcoylphénol, le ou les radicaux alcoyle du ou des alcoyphénols contenant de 9 à 28 atomes de carbone.
6. Procédé suivant la revendication 5, selon lequel la partie phénate hydrocarboné provient d'un alcoylphénol en C12 obtenu en alcoylant un phénol au moyen d'un tétramère de propylène.
7. Procédé suivant l'une quelconque des revendications précédentes, selon lequel il est incorporé au moins un acide carboxylique de formule (I) dans laquelle R est un radical alcoyle ou alcényle non ramifié.
8. Procédé suivant la revendication 7, selon lequel, dans l'acide carboxylique de la formule (1), R est un radical alcoyle à chaîne linéaire en C10 à C24 et R1 est l'hydrogène.
9. Procédé suivant l'une quelconque des revendications 1 à 6, selon lequel il est incorporé un mélange d'acides carboxyliques de formule (1), lequel mélange est d'une qualité commerciale contenant une variété d'acides, parmi lesquels à la fois des acides saturés et des acides insaturés.
10. Procédé suivant l'une quelconque des revendications 1 à 6, selon lequel il est incorporé de l'acide stéarique.
11. Procédé suivant l'une quelconque des revendications 1 à 6, selon lequel il est incorporé un acide dicarboxylique ou polycarboxylique contenant de 36 à 100 atomes de carbone ou un anhydride d'un tel acide.
12. Procédé suivant la revendication 11, selon lequel il est incorporé soit un acide polyisobutène-succinique, soit un anhydride polyisobutène-succinique.
13. Procédé suivant l'une quelconque des revendications précédentes, selon lequel (i) ou (ii) est incorporé dans le composant (b) dans une proportion supérieure à 10 à 35 % en poids, rapporté au poids du concentré.
14. Procédé suivant la revendication 13, selon lequel (i) ou (ii) est incorporé dans le composant (b) dans une proportion comprise entre 12 et 20 % en poids, rapporté au poids du concentré.
15. Procédé suivant l'une quelconque des revendications précédentes, selon lequel l'IAT du concentré est supérieur à 350.
16. Procédé suivant la revendication 15, selon lequel l'IAT du concentré est supérieur à 400.
17. Procédé suivant l'une quelconque des revendications précédentes, selon lequel la viscosité du concentré à 100 ° C est inférieure à 750 cSt.
18. Procédé suivant la revendication 17, selon lequel la viscosité du concentré à 100 ° C est inférieure à 500 mm2.s-1 (cSt).
19. Procédé suivant l'une quelconque des revendications précédentes, selon lequel le composant (B) est la chaux.
20. Procédé suivant l'une quelconque des revendications précédentes, selon lequel le rapport en poids du composant (B) au composant (A) est compris entre 0,2 et 5.
21. Procédé suivant l'une quelconque des revendications précédentes, selon lequel le composant (C) est l'éthylèneglycol.
22. Procédé suivant l'une quelconque des revendications 1 à 20, selon lequel le composant (C) est le méthyldigol.
23. Procédé suivant l'une quelconque des revendications précédentes, selon lequel l'anhydride carbonique (composant E) est ajouté à la suite d'une addition unique de composant (B) lors de l'achèvement de la réaction entre les composants (A) à (D) et (F).
24. Procédé suivant l'une quelconque des revendications précédentes, selon lequel un diluant est présent.
25. Procédé suivant l'une quelconque des revendications précédentes, selon lequel on ajoute au mélange de réaction du soufre en supplément par rapport à celui déjà présent au moyen du composant (A).
26. Procédé suivant l'une quelconque des revendications précédentes, selon lequel la réaction est conduite en présence d'un catalyseur.
27. Procédé suivant la revendication 26, selon lequel le catalyseur est un halogénure non organique.
28. Procédé suivant la revendication 27, selon lequel le catalyseur est le chlorure de calcium.
29. Composition d'huile lubrifiante constituant un produit fini, laquelle composition comprend une huile lubrifiante et suffisamment du concentré d'additif produit par le procédé suivant l'une quelconque des revendications précédentes pour donner un IAT compris entre 0,5 et 120.
30. Composition d'huile lubrifiante constituant un produit fini suivant la revendication 29, dans laquelle l'huile lubrifiante est une huile lubrifiante marine, suffisamment du concentré d'additif étant présent pour donner un IAT compris entre 9 et 100.
31. Composition d'huile lubrifiante constituant un produit fini suivant la revendication 29, dans laquelle l'huile lubrifiante est une huile lubrifiante pour moteur d'automobile, suffisamment du concentré d'additif étant présent pour donner un IAT compris entre 4 et 20.
32. Concentré d'additif convenant pour être incorporé dans une huile de lubrification constituant un produit fini, lequel concentré peut être obtenu en faisant réagir à température élevée (A) un phénate de métal alcalino-terreux, hydrocarboné et sulfuré, ayant un IAT inférieur à celui du concentré d'additif final, (B) une base de métal alcalino-terreux ajoutée soit en totalité aux produits réagissants initiaux, soit en partie à ces produits réagissants initiaux et le reste en une ou plusieurs portions à un stade ou des stades ultérieurs au cours du procédé, (C) un alcool polyhydrique ayant de 2 à 4 atomes de carbone, un diglycol ou triglycol en C2 à C4, un alcoyléther d'alcoylèneglycol ou un alcoyléther de polyalcoylèneglycol, (D) une huile lubrifiante, (E) de l'anhydride carbonique ajouté à la suite de l'addition, ou de chaque addition, de composant (B) et (F) suffisamment pour donner une proportion allant d'une valeur supérieure à 2 à 35 % en poids, rapporté au poids de concentré, soit (i) d'un acide carboxylique de formule (I) ou d'un anhydride ou un ester d'un tel acide, soit (ii) d'un acide dicarboxylique ou polycarboxylique contenant de 36 à 100 atomes de carbone, ou d'un anhydride ou un ester d'un tel acide, les rapports en poids des composants (A) à (F) étant tels qu'ils produisent un concentré ayant un IAT supérieur à 300 et une viscosité à 100 ° C inférieure à 1000 mm2.s-1 (cSt).
EP87310461A 1986-11-29 1987-11-26 Alkylphénates de métaux alcalino-terreux sulfurés, leur préparation et leur utilisation Expired - Lifetime EP0273588B2 (fr)

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Application Number Priority Date Filing Date Title
AT87310461T ATE79396T1 (de) 1986-11-29 1987-11-26 Geschwefelt erdalkalimetallalkylphenolate, ihre herstellung und ihre verwendung.

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Application Number Priority Date Filing Date Title
GB868628609A GB8628609D0 (en) 1986-11-29 1986-11-29 Lubricating oil additives
GB8628609 1986-11-29

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EP0273588A1 EP0273588A1 (fr) 1988-07-06
EP0273588B1 true EP0273588B1 (fr) 1992-08-12
EP0273588B2 EP0273588B2 (fr) 2001-03-28

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EP87310460A Expired - Lifetime EP0271262B2 (fr) 1986-11-29 1987-11-26 Alkylphénates de métaux alcalino-terreux, leurs dérivés sulfurés, leur préparation et leur utilisation

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JP (2) JPH0631383B2 (fr)
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CN (2) CN1012074B (fr)
AT (2) ATE79396T1 (fr)
AU (2) AU609075B2 (fr)
BR (2) BR8707550A (fr)
CA (2) CA1305697C (fr)
DE (2) DE3781126T3 (fr)
DK (2) DK175287B1 (fr)
ES (2) ES2051752T3 (fr)
FI (2) FI93653C (fr)
GB (1) GB8628609D0 (fr)
GR (2) GR3006075T3 (fr)
IN (2) IN172581B (fr)
MX (2) MX169105B (fr)
NO (2) NO176147C (fr)
SG (2) SG101192G (fr)
WO (2) WO1988003945A1 (fr)
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WO2011066141A2 (fr) 2009-11-30 2011-06-03 The Lubrizol Corporation Mélanges stabilisés contenant des modificateurs de friction
WO2011066145A1 (fr) 2009-11-30 2011-06-03 The Lubrizol Corporation Mélanges stabilisés contenant des modificateurs de friction
WO2011066059A1 (fr) 2009-11-30 2011-06-03 The Lubrizol Corporation Procédés pour maîtriser les taux de trioxyde de soufre dans des moteurs à combustion interne
WO2012109311A2 (fr) 2011-02-09 2012-08-16 The Lubrizol Corporation Compositions lubrifiantes contenant un dispersant asphaltène
WO2014172125A1 (fr) 2013-04-17 2014-10-23 The Lubrizol Corporation Composition lubrifiante de chemise de cylindre d'un moteur à combustion interne à deux temps

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GB8814008D0 (en) * 1988-06-14 1988-07-20 Bp Chemicals Additives Lubricating oil additives
GB8814010D0 (en) * 1988-06-14 1988-07-20 Bp Chemicals Addivites Ltd Lubricating oil additives
GB8814009D0 (en) * 1988-06-14 1988-07-20 Bp Chemicals Additives Lubricating oil additives
GB8814013D0 (en) * 1988-06-14 1988-07-20 Bp Chemicals Additives Chemical process
EP0385616B1 (fr) * 1989-02-25 1994-06-01 Bp Chemicals (Additives) Limited Procédé de production d'un concentré d'additif pour huile lubrifiante
GB8917094D0 (en) * 1989-07-26 1989-09-13 Bp Chemicals Additives Chemical process
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GB9213723D0 (en) * 1992-06-27 1992-08-12 Bp Chemicals Additives Process for the production of lubricating oil additives
JP2737096B2 (ja) * 1993-08-25 1998-04-08 株式会社コスモ総合研究所 過塩基性硫化アルカリ土類金属フェネートの製造法
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GB9325132D0 (en) * 1993-12-08 1994-02-09 Bp Chemicals Additives Lubricating oil additives
GB9400417D0 (en) * 1994-01-11 1994-03-09 Bp Chemicals Additives Lubricating oil composition
GB9400415D0 (en) * 1994-01-11 1994-03-09 Bp Chemicals Additives Detergent compositions
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CA2183906A1 (fr) * 1995-08-23 1997-02-24 Christopher S. Fridia Production d'un melange de phenate-stearate a faible teneur en sediments fins
EP0778336A1 (fr) * 1995-12-08 1997-06-11 Cosmo Research Institute Additif pour huile minérale ayant une stabilité excellente au stockage à la chaleur comprenant un sel de métal alcalino-terreux d'un acide aromatique hydroxycarboxylique ou un mélange sulfurisé de celle-ci
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GB9611317D0 (en) * 1996-05-31 1996-08-07 Exxon Chemical Patents Inc Overbased metal-containing detergents
GB9611316D0 (en) * 1996-05-31 1996-08-07 Exxon Chemical Patents Inc Overbased metal-containing detergents
US5728657A (en) * 1996-08-20 1998-03-17 Chevron Chemical Company Production of low fine sediment high TBN phenate stearate
EP0989178A4 (fr) * 1997-05-07 2000-09-13 Cosmo Sogo Kenkyusho Kk Composition d'huile lubrifiante, concentre de phenate de sulfure de metal alcalino-terreux hyperbasique utilise dans la preparation de cette composition et procede de preparation du concentre
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US6348438B1 (en) 1999-06-03 2002-02-19 Chevron Oronite S.A. Production of high BN alkaline earth metal single-aromatic ring hydrocarbyl salicylate-carboxylate
EP1710294B1 (fr) 2005-04-06 2013-03-06 Infineum International Limited Une méthode pour améliorer la stabilité ou la compatibilité des tensioactifs
EP1743933B1 (fr) 2005-07-14 2019-10-09 Infineum International Limited Utilisation pour améliorer la compatibilité d'un détergent avec des modificateurs de friction d'une composition lubrifiante
US20080153723A1 (en) 2006-12-20 2008-06-26 Chevron Oronite Company Llc Diesel cylinder lubricant oil composition
US20120266837A1 (en) 2009-08-06 2012-10-25 The Lubrizol Corporation Asphaltene Dispersant Containing Lubricating Compositions
SG191274A1 (en) 2010-12-21 2013-07-31 Lubrizol Corp Lubricating composition containing a detergent
JP5840233B2 (ja) 2011-02-17 2016-01-06 ザ ルブリゾル コーポレイションＴｈｅ Ｌｕｂｒｉｚｏｌ Ｃｏｒｐｏｒａｔｉｏｎ 良好なｔｂｎ保持率を有する潤滑剤
EP2607462B1 (fr) 2011-12-20 2014-03-12 Infineum International Limited Lubrification de moteur marin
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EP2674474B1 (fr) * 2012-06-13 2015-09-09 Infineum International Limited Préparation d'un détergent phénate
US10415153B2 (en) 2014-04-02 2019-09-17 Franck Natali Doped rare earth nitride materials and devices comprising same

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FR2549080B1 (fr) * 1983-07-11 1986-04-04 Orogil Procede de preparation d'additifs detergents-dispersants de tres haute alcalinite a base de calcium et additifs detergents-dispersants pour huiles lubrifiantes ainsi obtenus
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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011066141A2 (fr) 2009-11-30 2011-06-03 The Lubrizol Corporation Mélanges stabilisés contenant des modificateurs de friction
WO2011066145A1 (fr) 2009-11-30 2011-06-03 The Lubrizol Corporation Mélanges stabilisés contenant des modificateurs de friction
WO2011066144A1 (fr) 2009-11-30 2011-06-03 The Lubrizol Corporation Mélanges stabilisés contenant des modificateurs de friction
WO2011066059A1 (fr) 2009-11-30 2011-06-03 The Lubrizol Corporation Procédés pour maîtriser les taux de trioxyde de soufre dans des moteurs à combustion interne
WO2011066142A1 (fr) 2009-11-30 2011-06-03 The Lubrizol Corporation Mélanges stabilisés contenant des modificateurs de friction
WO2012109311A2 (fr) 2011-02-09 2012-08-16 The Lubrizol Corporation Compositions lubrifiantes contenant un dispersant asphaltène
WO2014172125A1 (fr) 2013-04-17 2014-10-23 The Lubrizol Corporation Composition lubrifiante de chemise de cylindre d'un moteur à combustion interne à deux temps

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EP0271262B2 (fr) 2002-05-29
NO883349D0 (no) 1988-07-28
EP0273588B2 (fr) 2001-03-28
BR8707551A (pt) 1989-03-14
KR890700159A (ko) 1989-03-10
FI883502A0 (fi) 1988-07-25
DE3781126T3 (de) 2001-08-02
AU8238087A (en) 1988-06-16
EP0273588A1 (fr) 1988-07-06
AU608792B2 (en) 1991-04-18
IN172581B (fr) 1993-10-16
EP0271262A1 (fr) 1988-06-15
NO883348L (no) 1988-09-14
FI93653B (fi) 1995-01-31
CN1012074B (zh) 1991-03-20
CN87108344A (zh) 1988-06-22
KR960010992B1 (ko) 1996-08-14
DE3781118D1 (de) 1992-09-17
DK175287B1 (da) 2004-08-09
JPH01501400A (ja) 1989-05-18
KR890700158A (ko) 1989-03-10
JPH0631384B2 (ja) 1994-04-27
EP0271262B1 (fr) 1992-08-12
ES2051751T3 (es) 1994-07-01
ES2051752T3 (es) 1994-07-01
CA1305697C (fr) 1992-07-28
FI883503A0 (fi) 1988-07-25
GR3006075T3 (fr) 1993-06-21
AU8237287A (en) 1988-06-16
FI93654C (fi) 1995-05-10
MX169106B (es) 1993-06-22
SG101092G (en) 1992-12-04
DE3781126D1 (de) 1992-09-17
JPH0631383B2 (ja) 1994-04-27
NO883349L (no) 1988-09-22
NO302763B1 (no) 1998-04-20
DK419888D0 (da) 1988-07-27
NO176147C (no) 1995-02-08
AU609075B2 (en) 1991-04-26
DE3781126T2 (de) 1993-03-04
CN87108239A (zh) 1988-06-15
FI883502A (fi) 1988-07-25
FI93653C (fi) 1995-05-10
ATE79395T1 (de) 1992-08-15
WO1988003944A1 (fr) 1988-06-02
GR3006112T3 (fr) 1993-06-21
NO176147B (no) 1994-10-31
CN1015642B (zh) 1992-02-26
ATE79396T1 (de) 1992-08-15
NO883348D0 (no) 1988-07-28
DK419888A (da) 1988-07-27
ZA878939B (en) 1989-07-26
DK419788D0 (da) 1988-07-27
ZA878938B (en) 1989-07-26
GB8628609D0 (en) 1987-01-07
BR8707550A (pt) 1989-03-14
WO1988003945A1 (fr) 1988-06-02
KR960010991B1 (ko) 1996-08-14
CA1305696C (fr) 1992-07-28
DE3781118T2 (de) 1992-12-17
MX169105B (es) 1993-06-22
IN169547B (fr) 1991-11-09
FI93654B (fi) 1995-01-31
JPH01501399A (ja) 1989-05-18
SG101192G (en) 1992-12-04
DK419788A (da) 1988-07-27
DE3781118T3 (de) 2002-08-14
FI883503A (fi) 1988-07-25

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