Bp Chemicals (additives) Limited

Bp Chemicals Limited

Michael J Clarke

John R Blackborow

Simon C Brown

This invention relates to novel pure hydrocarbyl succinylating agents, substantially pure derivatives thereof, to a method of preparation of pure substituted succinylating agents and their derivatives, and to the use of thereof as additives for fuels and lubricants. The hydrocarbyl substituted succinylating agents are pure because the real and apparent mole ratios of the succinyl groups to the hydrocarbyl groups in such agents are substantially the same. These are produced by reacting an olefin polymer such as poly(iso)butylene with maleic anhydride to form a hydrocarbyl substitued succinylating agent which is then cleaned by solvent extraction to remove any impurities therein before use in further reactions.

Resin-free succinimides process of making, and compositions containing

A fuel composition which comprises a major amount of a liquid hydrocarbon fuel and, in an amount to provide detergency, a polyisobutene (PIB) succinimide derived from the reaction of a polyisobutene--substituted succinic acylating agent and an amine having at least one reactive hydrogen bonded to an amine nitrogen is characterised in that the polyisobutene--substituted succinic acylating agent is obtained by a thermal route and the polyisobutene substituent is derived from a highly reactive polyisobutene ie having a high proportion of vinylidene groups --CH.sub.2 CMe.dbd.CH.sub.2. The PIB-substituted succinic acylating agent is preferably obtained by the thermal reaction of the highly reactive polyisobutene with a succinic acylating agent e.g. maleic anhydride.

Fuel compositions containing a polyisobutene succinimide detergent

Resin-free succinimides

Oxidized polyisobutenes, that is polyisobutenes containing ketonic and carboxylic acid carbonyl groups, are produced by passing through a column of the polyisobutene maintained at a temperature in the range from 140.degree. to 200.degree. C. and at atmospheric or elevated total pressure a molecular oxygen-containing gaseous oxidant at a gas flow rate greater than 10 liters cm.sup.-2 h.sup.-1 measured at the operating pressure. The oxidized polyisobutenes can be reacted for example with an aliphatic polyamine to produce a lubricating oil additive or with an aliphatic polyamide and formaldehyde to produce a fuels additive.

Process for the production of oxidized polyisobutenes, their use in the

A process for the preparation of a polyisobutene amine, in particularly a polyisobutene amine of formula (I): ##STR1## comprises reacting a carbonyl funtionalized polyisobutene [PIB]--(CO)R and an amine H.sub.2 NR.sup.1 and hydrogenating the product of the reaction between said carbonyll functionalized polyisobutene and said amine, where PIB is a polyisobutenyl group,

Process for the preparation of polyisobutene amines and fuel

Oxidised polyisobutenes, that is polyisobutenes containing ketonic and carboxylic acid carbonyl groups, are produced by passing through a column of the polyisobutene maintained at a temperature in the range from 140.degree. to 200.degree. C. and at atmospheric or elevated total pressure a molecular oxygen-containing gaseous oxidant at a gas flow rate greater than 10 liters cm.sup.-2 h.sup.-1 measured at the operating pressure. The oxidized polysisobutenes can be reacted for example with an aliphatic polyamine to produce a lubricating oil additive or with an aliphatic polyamine and formaldehyde to product a fuels additive.

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Hull, United Kingdom

Michael J Clarke