Abstract: Provided herein are functionalized branched alcohols comprising a glycosyl group, an ethylene oxide linker and a tail. The ethylene oxide linker comprises one or more units of ethylene oxide. The glycosyl group is a substituent structure of a cyclic monosaccharide. The tail comprises a branched paraffin or isomers thereof, the glycosyl group is attached to the ethylene oxide linker, and the ethylene oxide linker is attached to the tail. In an aspect, the glycosyl group is a substituent structure of glucose, mannose, galactose, sorbose, fructose, xylose, arabinose, ribose, lyxose, lactose, or maltose, or variants thereof. The tail can be a paraffin comprising 9 to 13 carbon atoms.

Abstract: Compositions comprising a sulfonated reaction product or a salt thereof may be prepared from a cyclohexylbenzene compound that has been alkylated with an olefin of formula R1R2CCH2, wherein R1 is a C6-C24 hydrocarbyl group, and R2 is H or a C6-C24 hydrocarbyl group. Methods for sulfonating an alkylated cyclohexylbenzene compound prepared from a cyclohexylbenzene compound that has been alkylated with an olefin of formula R1R2CCH2, wherein R1 is a C6-C24 hydrocarbyl group, and R2 is H or a C6-C24 hydrocarbyl group may comprise contacting the alkylated cyclohexylbenzene compound with a sulfonating reagent; forming a sulfonated reaction product; and converting the sulfonated reaction product into a sulfonate salt.

Abstract: Provided herein are novel extended branched alcohols having a lower branching number and improved biodegradability when compared to other branched alcohols. Also provided are novel extended branched ethoxylates having surfactant properties which can be more efficient in reducing surface tension when compared to the ethoxylated form of other branched alcohols. Further provided are novel syntheses of making extended branched alcohols and extended branched ethoxylates.

Abstract: Compositions comprising a sulfonated reaction product or a salt thereof may be prepared from a biphenyl compound that has been alkylated with an olefin of formula R1R2CCH2, wherein R1 is a C6-C24 hydrocarbyl group, and R2 is H or a C6-C24 hydrocarbyl group. Methods for sulfonating an alkylated biphenyl compound prepared from a biphenyl compound that has been alkylated with an olefin of formula R1R2CCH2, wherein R1 is a C6-C24 hydrocarbyl group, and R2 is H or a C6-C24 hydrocarbyl group may comprise contacting the alkylated biphenyl compound with a sulfonating reagent; forming a sulfonated reaction product; and converting the sulfonated reaction product into a sulfonate salt.

Abstract: Provided herein are functionalized branched alcohols comprising a glycosyl group, an ethylene oxide linker and a tail. The ethylene oxide linker comprises one or more units of ethylene oxide. The glycosyl group is a substituent structure of a cyclic monosaccharide. The tail comprises a branched paraffin or isomers thereof, the glycosyl group is attached to the ethylene oxide linker, and the ethylene oxide linker is attached to the tail. In an aspect, the glycosyl group is a substituent structure of glucose, mannose, galactose, sorbose, fructose, xylose, arabinose, ribose, lyxose, lactose, or maltose, or variants thereof. The tail can be a paraffin comprising 9 to 13 carbon atoms.

Abstract: Provided herein are novel extended branched alcohols having a lower branching number and improved biodegradability when compared to other branched alcohols. Also provided are novel extended branched ethoxylates having surfactant properties which can be more efficient in reducing surface tension when compared to the ethoxylated form of other branched alcohols. Further provided are novel syntheses of making extended branched alcohols and extended branched ethoxylates.

Abstract: Compositions comprising a sulfonated reaction product or a salt thereof may be prepared from a cyclohexylbenzene compound that has been alkylated with an olefin of formula R1R2CCH2, wherein R1 is a C6-C24 hydrocarbyl group, and R2 is H or a C6-C24 hydrocarbyl group. Methods for sulfonating an alkylated cyclohexylbenzene compound prepared from a cyclohexylbenzene compound that has been alkylated with an olefin of formula R1R2CCH2, wherein R1 is a C6-C24 hydrocarbyl group, and R2 is H or a C6-C24 hydrocarbyl group may comprise contacting the alkylated cyclohexylbenzene compound with a sulfonating reagent; forming a sulfonated reaction product; and converting the sulfonated reaction product into a sulfonate salt.

Abstract: Compositions comprising a sulfonated reaction product or a salt thereof may be prepared from a diphenyl ether compound that has been alkylated with an olefin of formula R1R2CCH2, wherein R1 is a C6-C24 hydrocarbyl group, and R2 is H or a C6-C24 hydrocarbyl group. Methods for sulfonating an alkylated diphenyl ether compound prepared from a diphenyl ether compound that has been alkylated with an olefin of formula R1R2CCH2, wherein R1 is a C6-C24 hydrocarbyl group, and R2 is H or a C6-C24 hydrocarbyl group may comprise contacting the alkylated diphenyl ether compound with a sulfonating reagent; forming a sulfonated reaction product; and converting the sulfonated reaction product into a sulfonate salt.

Abstract: Compositions comprising a sulfonated reaction product or a salt thereof may be prepared from a biphenyl compound that has been alkylated with an olefin of formula R1R2CCH2, wherein R1 is a C6-C24 hydrocarbyl group, and R2 is H or a C6-C24 hydrocarbyl group. Methods for sulfonating an alkylated biphenyl compound prepared from a biphenyl compound that has been alkylated with an olefin of formula R1R2CCH2, wherein R1 is a C6-C24 hydrocarbyl group, and R2 is H or a C6-C24 hydrocarbyl group may comprise contacting the alkylated biphenyl compound with a sulfonating reagent; forming a sulfonated reaction product; and converting the sulfonated reaction product into a sulfonate salt.

Abstract: This disclosure provides a method for improving or maintaining antioxidant performance of a lubricating oil in an engine or other mechanical component lubricated with the lubricating oil by using as the lubricating oil a formulated oil. The formulated oil has a composition including a lubricating oil base stock as a major component, and at least one functionalized quercetin antioxidant, as a minor component. The at least one functionalized quercetin antioxidant is soluble in the lubricating oil. Antioxidant performance is improved or maintained as compared to antioxidant performance achieved using a lubricating oil containing a phenolic or aminic antioxidant, as determined by Lubricant Oxidation Test as described herein or Catalytic Oxidation Test as described herein. This disclosure also relates to lubricating oils having at least one functionalized quercetin antioxidant.

Abstract: A lubricating oil including a lubricating oil base stock as a major component; and a mixture of (i) one or more protected lubricating oil additives having a first performance function, and (ii) one or more unprotected lubricating oil additives having a second performance function, as a minor component. The first performance function and the second performance function are the same. The one or more protected lubricating oil additives are inactive with respect to their performance function. The one or more protected lubricating oil additives are converted into one or more unprotected lubricating oil additives in the lubricating oil in-service in an engine or other mechanical component. A method for controlled release of one or more lubricating oil additives into a lubricating oil. A method for improving oxidative stability of a lubricating oil and extending performance life of one or more lubricating oil additives.

Abstract: A lubricating oil including a lubricating oil base stock as a major component, and one or more lubricating oil additives having at least one protected active group, as a minor component. The one or more lubricating oil additives having at least one protected active group are converted into one or more lubricating oil additives having at least one unprotected active group in the lubricating oil in-service in an engine or other mechanical component. Compositions including one or more lubricating oil additives having at least one protected active group. A method for improving solubility of one or more lubricating oil additives in a lubricating oil. A method for improving oxidative stability of a lubricating oil and extending performance life of one or more lubricating oil additives. A method for improving friction control in an engine or other mechanical component lubricated with a lubricating oil.

Abstract: A composition that includes one or more compounds represented by the formula R1—O—R2 wherein R1 is a substituted or unsubstituted aryl or polyaryl group having from about 4 to about 40 carbon atoms, and R2 is a substituted or unsubstituted, linear or branched, alkyl group having from about 4 to about 40 carbon atoms. The composition has a viscosity (Kv100) from about 1 to about 10 cSt at 100° C. as determined by ASTM D-445, a viscosity index (VI) from about ?100 to about 300 as determined by ASTM D-2270, and a Noack volatility of no greater than 50 percent as determined by ASTM D-5800. The disclosure also relates to a process for producing the composition, a lubricating oil base stock and lubricating oil containing the composition, and a method of reducing boundary friction and improving dispersancy of polar additives of a lubricating oil by using as the lubricating oil a formulated oil containing the composition.

Abstract: A lubricating oil including a lubricating oil base stock as a major component; and a mixture of (i) one or more protected lubricating oil additives having a first performance function, and (ii) one or more unprotected lubricating oil additives having a second performance function, as a minor component. The first performance function and the second performance function are the same. The one or more protected lubricating oil additives are inactive with respect to their performance function. The one or more protected lubricating oil additives are converted into one or more unprotected lubricating oil additives in the lubricating oil in-service in an engine or other mechanical component. A method for controlled release of one or more lubricating oil additives into a lubricating oil. A method for improving oxidative stability of a lubricating oil and extending performance life of one or more lubricating oil additives.

Abstract: A lubricating oil including a lubricating oil base stock as a major component, and one or more lubricating oil additives having at least one protected active group, as a minor component. The one or more lubricating oil additives having at least one protected active group are converted into one or more lubricating oil additives having at least one unprotected active group in the lubricating oil in-service in an engine or other mechanical component. Compositions including one or more lubricating oil additives having at least one protected active group. A method for improving solubility of one or more lubricating oil additives in a lubricating oil. A method for improving oxidative stability of a lubricating oil and extending performance life of one or more lubricating oil additives. A method for improving friction control in an engine or other mechanical component lubricated with a lubricating oil.

Abstract: A composition that includes one or more compounds represented by the formula R1—O—R2 wherein R1 is a substituted or unsubstituted aryl or polyaryl group having from about 4 to about 40 carbon atoms, and R2 is a substituted or unsubstituted, linear or branched, alkyl group having from about 4 to about 40 carbon atoms. The composition has a viscosity (Kv100) from about 1 to about 10 cSt at 100° C. as determined by ASTM D-445, a viscosity index (VI) from about ?100 to about 300 as determined by ASTM D-2270, and a Noack volatility of no greater than 50 percent as determined by ASTM D-5800. The disclosure also relates to a process for producing the composition, a lubricating oil base stock and lubricating oil containing the composition, and a method of reducing boundary friction and improving dispersancy of polar additives of a lubricating oil by using as the lubricating oil a formulated oil containing the composition.