US2003131527A1PendingUtilityA1

Alkyl-substituted aryl polyalkoxylates and their use in fuels

Assignee: ETHYL CORPPriority: Jan 17, 2002Filed: Jan 17, 2002Published: Jul 17, 2003
Est. expiryJan 17, 2022(expired)· nominal 20-yr term from priority
C10L 1/1905C10L 1/305C10L 10/04C10L 1/1985C10L 1/2383C10L 1/2387C10L 1/238C10L 1/1832C08G 65/2612C10L 1/2437C10L 1/143C10L 1/1881C10L 1/223
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Claims

Abstract

The present invention relates to an alkyl-substituted aryl polyalkoxylate composition, fuel concentrates, and fuel compositions containing the composition. The invention further relates to the use of the alkyl-substituted aryl polyalkoxylate composition in fuel combusted in engines to reduce the formation of intake valve deposits and to reduce valve sticking in the engines.

Claims

exact text as granted — not AI-modified
What is claimed:  
     
         1 . A alkyl-substituted aryl polyalkoxylate of the formula  
       R—(Ar) n —(O-A) m —OH  
       where 
 R is a polyalkene radical derived from C 2 - to C 20 -alkenes and having a number average molecular weight of from about 200 to about 5,000;  
 Ar is selected from a phenylene group, a substituted phenylene group, and a polynuclear aromatic group;  
 A is an alkylene group of 2 to 8 carbon atoms;  
 m is a number up to 200; and  
 n is or 2.  
 
     
     
         2 . An alkyl-substituted aryl polyalkoxylate as claimed in  claim 1 , in which R is a polybutyl or polyisobutyl radical derived from isobutene and up to about 20 percent by weight of n-butene and having a number average molecular weight of from about 200 to about 2500.  
     
     
         3 . An alkyl-substituted aryl polyalkoxylate as claimed in  claim 1 , in which R is a polybutyl or polyisobutyl radical having a number average molecular weight of from about 400 to about 1250.  
     
     
         4 . An alkyl-substituted aryl polyalkoxylate as claimed in  claim 1 , in which R is a polybutyl or polyisobutyl radical having a number average molecular weight of from about 450 to about 1000.  
     
     
         5 . An alkyl-substituted aryl polyalkoxylate as claimed in  claim 1 , in which m is a number up to about 45.  
     
     
         6 . An alkyl-substituted aryl polyalkoxylate as claimed in  claim 1 , in which A is 1,2-propylene and/or 1,2-butylene.  
     
     
         7 . An alkyl-substituted aryl polyalkoxylate as claimed in  claim 1 , in which Ar is a phenol.  
     
     
         8 . An alkyl-substituted aryl polyalkoxylate as claimed in  claim 1 , in which Ar is a hydrocarbon-substituted phenol.  
     
     
         9 . An alkyl-substituted aryl polyalkoxylate as claimed in  claim 1 , in which Ar is a cresol.  
     
     
         10 . An alkyl-substituted aryl polyalkoxylate as claimed in  claim 1 , in which Ar is a hydrocarbon-substituted cresol.  
     
     
         11 . A fuel additive concentrate comprising an alkyl-substituted aryl polyalkoxylate of  claim 1  in an amount of from about 0.1 to about 80% by weight.  
     
     
         12 . A fuel additive concentrate comprising an alkyl-substituted aryl polyalkoxylate of  claim 1  in an amount of from about 0.5 to about 60% by weight.  
     
     
         13 . A fuel composition comprising an alkyl-substituted aryl polyalkoxylate of  claim 1 , and a fuel.  
     
     
         14 . The composition of  claim 13 , wherein the fuel is gasoline.  
     
     
         15 . The composition of  claim 13 , wherein the fuel is diesel fuel.  
     
     
         16 . The composition of  claim 13 , wherein the fuel is burner fuel.  
     
     
         17 . The composition of  claim 13 , wherein the fuel is jet fuel.  
     
     
         18 . A process for reducing the formation of intake valve deposits in a gasoline engine, comprising combusting in a gasoline engine having intake valves a fuel composition comprising a gasoline fuel and an alkyl-substituted aryl polyalkoxylate of the formula  
       R—(Ar) n —(O-A) m —OH  
       where 
 R is a polyalkene radical derived from C 2 - to C 20 -alkenes and having a number average molecular weight of from about 200 to about 5,000;  
 Ar is selected from a phenylene group, a substituted phenylene group, and a polynuclear aromatic group;  
 A is an alkylene group of 2 to 8 carbon atoms;  
 m is a number up to 200; and  
 n is 1 or 2,  
 whereby the amount of deposits formed on the intake valves are reduced relative to the amount of deposits formed on the intake valves when the fuel composition combusted in the engine does not comprise the alkyl-substituted aryl polyalkoxylate.  
 
     
     
         19 . A process for reducing the valve sticking in a gasoline engine, comprising combusting in a gasoline engine having intake valves a fuel composition comprising a gasoline fuel and an alkyl-substituted aryl polyalkoxylate of the formula  
       R—(Ar) n —(O-A) m —OH  
       where 
 R is a polyalkene radical derived from C 2 - to C 20 -alkenes and having a number average molecular weight of from about 200 to about 5,000;  
 Ar is selected from a phenylene group, a substituted phenylene group, and a polynuclear aromatic group;  
 A is an alkylene group of 2 to 8 carbon atoms;  
 m is a number up to 200; and  
 n is 1 or2,  
 whereby the amount of sticking of the intake valves is reduced relative to the amount of sticking of the intake valves when the fuel composition combusted in the engine does not comprise the alkyl-substituted aryl polyalkoxylate.  
 
     
     
         20 . The composition of  claim 13 , further comprising a detergent.  
     
     
         21 . The composition of  claim 20 , wherein the detergent is selected from polyisobuteneamines, hydroxyl-containing polyisobuteneamines, polyetheramines, and polyalkenyl Mannich bases.  
     
     
         22 . The composition of  claim 20 , wherein the detergent is a polyalkenyl Mannich base.  
     
     
         23 . The composition of  claim 20 , further comprising one or more components selected from alkali metal salts of carboxylic acids or esters, alkaline earth metal salts of carboxylic acids or esters, alkali metal salts of sulfosuccinic acids or esters, alkaline earth metal salts of sulfosuccinic acids or esters, diluents, corrosion inhibitors, film-forming ammonium salts of organic carboxylic acids or esters, heterocyclic aromatics, antioxidants, stabilizers, demulsifiers, antistatic agents, metaliocenes, lubricity additives, and markers.

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