C07C303/42

Free-Solvent-Free Lithium Sulfonamide Salt Compositions That Are Liquid at Room Temperature, and Uses Thereof In Lithium Ion Battery
20200280098 · 2020-09-03 ·

Free-solvent-free lithium sulfonimide salt compositions that are liquid at room temperature, and methods of making free-solvent-free liquid lithium sulfonimide salt compositions. In an embodiment, the methods include mixing one or more lithium sulfonimide salts with one or more ether-based solvents and then removing the free solvent(s) under suitable vacuum, temperature, and time conditions so as to obtain a free-solvent-free liquid lithium sulfonimide salt composition that is liquid at room temperature. In an embodiment, the only solvent molecules that remain in the liquid lithium sulfonimide salt composition are adducted with lithium sulfonimide salt molecules. An example automated processing system for making free-solvent-free liquid lithium sulfonimide salts is also disclosed.

Free-Solvent-Free Lithium Sulfonamide Salt Compositions That Are Liquid at Room Temperature, and Uses Thereof In Lithium Ion Battery
20200280098 · 2020-09-03 ·

Free-solvent-free lithium sulfonimide salt compositions that are liquid at room temperature, and methods of making free-solvent-free liquid lithium sulfonimide salt compositions. In an embodiment, the methods include mixing one or more lithium sulfonimide salts with one or more ether-based solvents and then removing the free solvent(s) under suitable vacuum, temperature, and time conditions so as to obtain a free-solvent-free liquid lithium sulfonimide salt composition that is liquid at room temperature. In an embodiment, the only solvent molecules that remain in the liquid lithium sulfonimide salt composition are adducted with lithium sulfonimide salt molecules. An example automated processing system for making free-solvent-free liquid lithium sulfonimide salts is also disclosed.

WEAKLY COLOURED SULFONIC ACID
20200181072 · 2020-06-11 · ·

The subject of the present invention is a weakly corrosive and weakly coloured sulfonic acid, with an APHA colour index of less than 20, comprising chlorides and nitrites in a chloride/sulfonic acid molar ratio of between 1 ppm and 200 ppm, and a nitrite/sulfonic acid molar ratio of between 200 ppm and 6000 ppm, limits inclusive.

WEAKLY COLOURED SULFONIC ACID
20200181072 · 2020-06-11 · ·

The subject of the present invention is a weakly corrosive and weakly coloured sulfonic acid, with an APHA colour index of less than 20, comprising chlorides and nitrites in a chloride/sulfonic acid molar ratio of between 1 ppm and 200 ppm, and a nitrite/sulfonic acid molar ratio of between 200 ppm and 6000 ppm, limits inclusive.

ORGANIC REACTIONS CARRIED OUT IN AQUEOUS SOLUTION IN THE PRESENCE OF A HYDROXYALKYL(ALKYL)CELLULOSE OR AN ALKYLCELLULOSE

The present invention relates to a method of carrying out an organic reaction in aqueous solution in the presence of a hydroxyalkyl(alkyl)cellulose or an alkylcellulose.

ORGANIC REACTIONS CARRIED OUT IN AQUEOUS SOLUTION IN THE PRESENCE OF A HYDROXYALKYL(ALKYL)CELLULOSE OR AN ALKYLCELLULOSE

The present invention relates to a method of carrying out an organic reaction in aqueous solution in the presence of a hydroxyalkyl(alkyl)cellulose or an alkylcellulose.

AMINO-QUINONE ANTIPOLYMERANTS AND METHODS OF USING
20200102408 · 2020-04-02 ·

Described are methods and composition for inhibiting polymerization of a monomer (e.g., styrene) composition using an aminated quinone antipolymerant, such as an aminated benzoquinone or aminated naphthoquinone antipolymerant having one or more secondary or tertiary amine group(s). The aminated quinone antipolymerant can be used with little or no nitroxyl group containing antipolymerant yet still provide excellent antipolymerant activity in a monomer-containing composition.

AMINO-QUINONE ANTIPOLYMERANTS AND METHODS OF USING
20200102408 · 2020-04-02 ·

Described are methods and composition for inhibiting polymerization of a monomer (e.g., styrene) composition using an aminated quinone antipolymerant, such as an aminated benzoquinone or aminated naphthoquinone antipolymerant having one or more secondary or tertiary amine group(s). The aminated quinone antipolymerant can be used with little or no nitroxyl group containing antipolymerant yet still provide excellent antipolymerant activity in a monomer-containing composition.

Stable alkyl benzidine composition and methods of making and using same
10597352 · 2020-03-24 · ·

Stable formulations of alkyl benzidine compounds and methods of making and using same. To prepare a stable formulation, a short chain diol having fewer than six carbon atoms and an alkyl benzidine compound are combined together in solution at low pH and the solution is heated with moderate heat in the range of about 50 C. to 80 C. The stable formulation may contain dimers and/or trimers of the short chain diol. The stable formulation can be used to detect total chlorine in aqueous solution, to detect total chlorine in dialysis water, or as a colorimetric substrate in enzyme-linked immunosorbent assays.

Stable alkyl benzidine composition and methods of making and using same
10597352 · 2020-03-24 · ·

Stable formulations of alkyl benzidine compounds and methods of making and using same. To prepare a stable formulation, a short chain diol having fewer than six carbon atoms and an alkyl benzidine compound are combined together in solution at low pH and the solution is heated with moderate heat in the range of about 50 C. to 80 C. The stable formulation may contain dimers and/or trimers of the short chain diol. The stable formulation can be used to detect total chlorine in aqueous solution, to detect total chlorine in dialysis water, or as a colorimetric substrate in enzyme-linked immunosorbent assays.