US2017107438A1PendingUtilityA1

High molecular weight imide containing quaternary ammonium salts

Assignee: LUBRIZOL CORPPriority: May 30, 2014Filed: May 29, 2015Published: Apr 20, 2017
Est. expiryMay 30, 2034(~7.8 yrs left)· nominal 20-yr term from priority
C10L 2200/0423C10M 2217/043C10L 2200/0259C10L 10/18C10M 2215/04C10M 2215/02C10M 2215/042C10M 2207/127C10N 2040/25C10N 2040/252C10L 10/04C10N 2020/04C10L 1/2383C10M 2215/28C10L 2200/0446C10L 2270/023C10N 2040/253C10N 2040/26C10N 2070/00C10L 1/232C10M 133/56C10N 2040/255C10L 2270/026C10M 133/44C10N 2030/04C10L 1/1883C10M 2215/223C10N 2240/10C10N 2230/04C10N 2220/021
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Claims

Abstract

The present technology is related to imide containing quaternary ammonium salts having a hydrocarbyl substituent of number average molecular weight of 1300 to 3000, and the use of such quaternary ammonium salts in fuel compositions or lubricating compositions to improve the water shedding performance of the fuel or lubricant composition.

Claims

exact text as granted — not AI-modified
What we claim: 
     
         1 . A composition comprising an imide containing quaternary ammonium salt (“imide quat”), wherein the imide quat comprises the reaction product of:
 a) a quaternizable compound that is the reaction product of:
 (i) a hydrocarbyl-substituted acylating agent, wherein the hydrocarbyl-substituent has a number average molecular weight ranging from 1300 to 3000, and 
 (ii) a nitrogen containing compound having a nitrogen atom capable of reacting with said hydrocarbyl-substituted acylating agent to form an imide, and further having at least one quaternizable amino group; and 
 
 b) a quaternizing agent suitable for converting the quaternizable amino group of the nitrogen containing compound to a quaternary nitrogen. 
 
     
     
         2 . The composition of  claim 1 , wherein the quaternizable amino group is a primary, secondary or tertiary amino group. 
     
     
         3 . The composition of any previous claim, wherein the hydrocarbyl-substituted acylating agent comprises at least one polyisobutenyl succinic anhydride or polyisobutenyl succinic acid. 
     
     
         4 . The composition of any previous claim, wherein the reaction of a)(i) with a)(ii) is carried out at a temperature of greater than 80° C. 
     
     
         5 . The composition of any previous claim wherein the nitrogen containing compound excludes dimethylaminopropylamine. 
     
     
         6 . The composition of any previous claim, wherein the quaternizing agent comprises at least one dialkyl sulfate, alkyl halide, hydrocarbyl substituted carbonate, hydrocarbyl epoxide, carboxylate, alkyl ester or mixtures thereof. 
     
     
         7 . The composition of  claim 6 , wherein the quaternizing agent is a hydrocarbyl epoxide. 
     
     
         8 . The composition of  claim 7 , wherein the quaternizing agent is a hydrocarbyl epoxide in combination with an acid. 
     
     
         9 . The composition of  claim 6 , wherein the quaternizing agent is an oxalate or terephthalate. 
     
     
         10 . The composition of any previous claim wherein the quaternizing agent excludes methyl salicylate. 
     
     
         11 . The composition of any previous claim, further comprising at least one other additive. 
     
     
         12 . The composition of  claim 11 , wherein the at least one other additive comprises a detergent, a dispersant, a demulsifier, a lubricity agent, a cold flow improver, an antioxidant, or a mixture thereof. 
     
     
         13 . The composition of  claim 11 , wherein the at least one other additive comprises at least one hydrocarbyl-substituted succinic acid. 
     
     
         14 . The composition of  claim 11 , wherein the at least one other additive comprises at least one hydrocarbyl-substituted quaternary ammonium salt. 
     
     
         15 . The composition of  claim 11 , wherein the at least one other additive comprises at least one detergent/dispersant that is an amphiphilic substance which possess at least one hydrophobic hydrocarbon radical with a number average molecular weight of 100 to 10000 and at least one polar moiety selected from (i) Mono- or polyamino groups having up to 6 nitrogen atoms, at least one nitrogen atom having basic properties; (ii) Hydroxyl groups in combination with mono or polyamino groups, at least one nitrogen atoms having basic properties; (v) Polyoxy-C 2  to C 4  alkylene moieties terminated by hydroxyl groups, mono- or polyamino groups, at least one nitrogen atom having basic properties, or by carbamate groups; (vii) Moieties derived from succinic anhydride and having hydroxyl and/or amino and/or amido and/or imido groups; and/or (viii) Moieties obtained by Mannich reaction of substituted phenols with aldehydes and mono- or polyamines. 
     
     
         16 . The composition of  claims 13  through  15 , wherein the hydrocarbyl-substituent is a polyisobutylene having a molecular weight of from about 100 to about 5000. 
     
     
         17 . The composition of  claim 11 , wherein the at least one other additive comprises at least one Mannich compound. 
     
     
         18 . The composition of any previous claim, further comprising a fuel that is liquid at room temperature. 
     
     
         19 . The composition of  claim 18 , wherein the fuel is gasoline or diesel. 
     
     
         20 . The fuel composition of  claim 18  or  19  further comprising at least one of a low number average molecular weight soap, a low number average molecular weight polyisobutylene succinimide (PIBSI), or a mixture thereof. 
     
     
         21 . The fuel composition of  claims 18  through  20 , further comprising a low number average molecular weight soap with a number average molecular weight (M n ) of less than 340. 
     
     
         22 . The fuel composition of  claims 18  through  20 , further comprising from 0.01 to 25 ppm of a metal and from 1 to 12 ppm of a corrosion inhibitor. 
     
     
         23 . The fuel composition of  claim 22 , wherein the corrosion inhibitor is an alkenyl succinic acid comprising at least one of dodecenyl succinic acid (DDSA), hexadecenyl succinic acid (HDSA), or mixtures thereof. 
     
     
         24 . The fuel composition of  claims 18  through  20 , wherein the fuel comprises PIBSI with a low number average molecular weight M n  of less than 400. 
     
     
         25 . A method of improving water shedding performance of a fuel composition comprising employing a composition comprising an imide quat according to any  claims 1  to  24 . 
     
     
         26 . The composition of any of  claims 1  to  17 , further comprising an oil of lubricating viscosity. 
     
     
         27 . A method of operating an internal combustion engine comprising:
 a) supplying to said engine:
 (i) a fuel, wherein said fuel
 1. is liquid at room temperature; and 
 2. has a composition comprising an imide quat according to any  claims 1  to  17  therein; and 
 
   b) operating said engine.   
     
     
         28 . A method of operating an internal combustion engine comprising:
 a) supplying to a crankcase of said engine:
 (i) an oil of lubricating viscosity having a composition comprising an imide quat according to any  claims 1  to  17  therein, and 
   b) operating said engine.   
     
     
         29 . The method of  claim 28  wherein the oil of lubricating viscosity has total sulfated ash of less than 1 wt % and/or a phosphorus content of less than 0.11 wt %. 
     
     
         30 . A method of reducing and/or preventing injector deposits comprising:
 a) supplying to a fuel injector of said engine:
 (i) a fuel, wherein said fuel
 1. is liquid at room temperature; and 
 2. has a composition comprising an imide quat according to any  claims 1  to  17  therein; and 
 
   b) operating said engine.   
     
     
         31 . The method of  claim 30 , wherein the deposits comprise a low number average molecular weight soap, a low number average molecular weight polyisobutylene succinimide (PIBSI), or mixtures thereof. 
     
     
         32 . The method of  claim 31  wherein the fuel comprises a low number average molecular weight soap with a number average molecular weight (M n ) of less than 340. 
     
     
         33 . The method of  claims 30  through  32  wherein the fuel comprises from 0.01 to 25 ppm of a metal and from 1 to 12 ppm of a corrosion inhibitor. 
     
     
         34 . The method of  claim 33  wherein the corrosion inhibitor is an alkenyl succinic acid comprising at least one of dodecenyl succinic acid (DDSA), hexadecenyl succinic acid (HDSA), or mixtures thereof. 
     
     
         35 . The method of  claim 30 , wherein the fuel comprises a PIBSI with a low number average molecular weight M n  of less than 400. 
     
     
         36 . The method of  claims 30  to  36 , wherein the fuel is gasoline or diesel. 
     
     
         37 . The method of any of  claims 27  to  35  wherein the engine comprises a high pressure common rail injector system. 
     
     
         38 . The use of composition of any of  claims 1  to  17  to reduce and/or prevent internal deposits in an engine operated with a fuel, wherein the fuel is gasoline or diesel. 
     
     
         39 . The use of  claim 38  wherein the engine comprises a high pressure common rail injector system. 
     
     
         40 . The use of  claim 38  or  39  wherein said deposits are internal diesel injector deposits (IDID) deposits.

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