Abstract: A lubricating oil composition having a total base number of more than 15 mg KOH/g including oil of lubricating viscosity; detergent; and at least one compound of the formula (I) and/or formula (II): wherein Ar and Ar? represent substituted or unsubstituted aromatic moieties; L and L? are linking moieties; each Y is independently —ORI?or H(O(CR12)n)yX—, wherein X is (CR1?2)z, O or S; R1 and R1? are H, alkyl or aryl; R1? is alkyl or aryl; each Y? is independently Z(O(CR22)n?)y?X?—, wherein X? is (CR2?2)z?, O or S; R2 and R2? are H, alkyl or aryl; Z is H, acyl, alkyl or aryl; z and z? are 1 to 10; n is 0 to 10 when X is (CR1?2)z and 2 to 10 when X is O or S; n? is 0 to 10 when X? is (CR2?2)z?, and 2 to 10 when X? is O or S; y and y? are 1 to 30; a and a? are 0 to 3; and m and m? are 1 to 100, with the proviso that in compounds of formula (I), at least one Ar moiety bears at least one group Y and that in compounds of formula (II), at least one Ar? moiety bears at least one group Y? in wherein Z is not H.

Abstract: The residual chlorine content of a polyolefin-substituted carboxylic acylating agent formed by a halogen-assisted reaction of a polyalkene and at least one olefinic, monounsaturated mono- or dicarboxylic acid, anhydride or ester, is reduced when the reaction is conducted in the presence of a controlled amount of a metal compound.

Abstract: A trunk piston or cross-head diesel engine having a centrifuge system including a sealing medium is lubricated with a lubricant which, for the cross-head engine, is a system lubricant and which contains 0.04 to 5 mass %, expressed as active ingredient, of a combination of one or more linked aromatic compounds and one or more nitrogen containing ashless disperants, in a mass:mass ratio in the range of 1:3 to 9:1.

Abstract: The residual chlorine content of a polyolefin-substituted carboxylic acylating agent formed by a halogen-assisted reaction of a polyalkene and at least one olefinic, monounsaturated mono- or dicarboxylic acid, anhydride or ester, is reduced when the reaction is conducted in the presence of a controlled amount of a metal compound.

Abstract: A lubricating oil composition having a total base number of more than 15 mg KOH/g, as determined by ASTM D2896, and including at least 40 mass % of an oil of lubricating viscosity; at least one detergent; and at least one compound of the formula (I) and/or formula (II): In formula (I), each Ar independently represents an aromatic moiety having 0 to 3 substituents selected from the group consisting of alkyl, alkoxy, alkoxyalkyl, aryloxy, aryloxyalkyl, hydroxy, hydroxyalkyl, halo and combinations thereof; each L is independently a linking moiety comprising a carbon-carbon single bond or a linking group; each Y is independently —OR1? or a moiety of the formula H(O(CR12)n)yX—, wherein X is selected from the group consisting of (CR1?2)z, O and S; R1 and R1? are each independently selected from H, C1 to C6 alkyl and aryl; R1? is selected from C1 to C100 alkyl and aryl; z is 1 to 10; n is 0 to 10 when X is (CR1?2)z, and 2 to 10 when X is O or S; and y is 1 to 30; each a is independently 0 to 3, with the proviso

Abstract: A process for forming an ene reaction product wherein an enophile, such as maleic anhydride, is reacted with reactive polyalkene having a terminal vinylidene content of at least 30 mol. %, at high temperature in the presence of a free radical inhibitor. The polyalkenyl acylating agents are useful per se as additives in lubricating oils, functional fluids, and fuels and also serve as intermediates in the preparation of other products (e.g., succinimides) useful as additives in lubricating oils, functional fluids, and fuels. The presence of the free radical inhibitor during the high temperature reaction results in a reaction product that is low, or substantially free from sediment.

Abstract: A process for producing polyalkenyl acylating agent, wherein, upon completion of the thermal reaction of a polyalkene and an unsaturated mono- or dicarboxylic acid or anhydride compound, the reaction mixture is allowed to cool to below the reaction temperature, an additional amount of unsaturated mono- or dicarboxylic acid or anhydride compound is added to the cooled reaction mixture, which is then maintained in the reactor for a time period, optionally with agitation. Reducing the temperature of the reaction mixture prior to the introduction of additional unsaturated mono- or dicarboxylic acid or anhydride compound minimizes further reaction between the additional unsaturated mono- or dicarboxylic acid or anhydride compound and any remaining unreacted polyalkene, as well as self-polymerization of the unsaturated mono- or dicarboxylic acid or anhydride compound.

Abstract: A process for producing polyalkenyl acylating agent, wherein, upon completion of the thermal reaction of a polyalkene and an unsaturated mono- or dicarboxylic acid or anhydride compound, the reaction mixture is allowed to cool to below the reaction temperature, an additional amount of unsaturated mono- or dicarboxylic acid or anhydride compound is added to the cooled reaction mixture, which is then maintained in the reactor for a time period, optionally with agitation. Reducing the temperature of the reaction mixture prior to the introduction of additional unsaturated mono- or dicarboxylic acid or anhydride compound minimizes further reaction between the additional unsaturated mono- or dicarboxylic acid or anhydride compound and any remaining unreacted polyalkene, as well as self-polymerization of the unsaturated mono- or dicarboxylic acid or anhydride compound.

Abstract: A process for forming an ene reaction product wherein an enophile, such as maleic anhydride, is reacted with reactive polyalkene having a terminal vinylidene content of at least 30 mol. %, at high temperature in the presence of a free radical inhibitor. The polyalkenyl acylating agents are useful per se as additives in lubricating oils, functional fluids, and fuels and also serve as intermediates in the preparation of other products (e.g., succinimides) useful as additives in lubricating oils, functional fluids, and fuels. The presence of the free radical inhibitor during the high temperature reaction results in a reaction product that is low, or substantially free from sediment.

Abstract: Sulphonates are prepared by the neutralisation of a sulphonic acid with a basic hydroxide or oxide. The process requires the staged addition of sulphonic acid to a reaction mixture comprising basic hydroxide or oxide dispersed in a water/diluent mixture; the reaction mixture is basic throughout the additions of acid and at least until the point of completion of the neutralisation reaction. The basic hydroxide or oxide may also be added in stages. The sulphonate product has low viscosity, low haze and good stability and is essentially chloride free as halide promoters are not utilised in the manufacture of the product.

Abstract: Sulphonates are prepared by the neutralization of a sulphonic acid with a basic hydroxide or Oxide. The process requires the staged addition of sulphonic acid to a reaction mixture comprising basic hydroxide or oxide dispersed in water/diluent mixture; the reaction mixture is basic throughout the additions of acid and at least until the point of completion of the neutralization reaction. The basic hydroxide or oxide may also be added in stages. The sulphonate product has low viscosity, low haze and good stability and is essentially chloride free as halide promoters are not utilized in the manufacture of the product.