Abstract:
STABILIZED COMPOSITIONS COMPRISING AN ALKALI METAL FLUORIDE AND OZONE DERIVATIVE SELECTED FROM THE GROUP CONSISTING OF OXOLANE OF THE FORMULA:
3-R1,3-R2,5-R3,5-R4-1,2,4-TRIOXOLANE
AND ALKOXYHYDROPEROXIDES OF THE FORMULA:
R1-C(-R2)(-O-R5)-O-OH AND R3-C(-R4)(-O-R5)-O-OH
WHERE R1, R2, R3 AND R4 ARE HYDROGEN OR HYDROCARBYL AND R5 IS ALKYL AND A METHOD OF PRODUCING SAID STABILIZED OXOLANES AND HYDROPEROXIDES COMPRISING CONTACTING IN THE PRESENCE OF AN ALKALI METAL FLUORIDE AND OELFIN OF THE FORMULA
R1R2C=CR3R4
WITH OZONE OR OZONE AND ALKANOL OF THE FORMULA R5OH.
3,4-(-R8-)-1,2,4-TRIOXOLANE OR RX-C(-OOH)(-RY)-O-R10
IN THE PRESENCE OF A MOLYBDENUM, TUNGSTEN OR VANADIUM OXIDE-FORMING CTALYST WHERE R1, R2, R3 ARE ALKYL, ARYL, ALKYLARYL AND ARYLALKYL, R4 IS HYDROGEN OR ALKYL; R5, R6, R7, R8, RX, RY ARE HYDROGEN, ALKYL, ARYL, ALKYLARYL AND ARYLALKYL, R9 IS A, $ ALKYLENE AND R10 IS ALKYL OR ACYL. WITH AN OZONE DERIVATIVE OF THE FORMULA:
R1-N(-R2)-R3 OR R4-PYRIDINE
COMPRISING CONTACTING A TERTIARY AMINE OF THE FORMULA:
R1-N(-R2)(-R3)(=O) OR 1-(O=),R4-PYRIDINE
METHOD OF PREPARING TERIOTARY AMINE OXIDE OF THE FORMULA:
Abstract:
Z IS HYDROGEN OR X, R1, R2 AND R3 ARE HYDROGEN OR ALKYL, R IS AS HERETOFORE DEFINEDWITH OZONE AND ALKANOIC ACID AND THEN CONTACTING THE RESULTANT REACTION MIXTURE WITH MINERAL ACID AND WATER.
-C(-R1)=C(-R2)-R3
WHERE X IS
R,Z,X-BENZENE
WHERE R IS HYDROGEN OR ALKYL AND Y IS HYDROGEN OR-OH COMPRISING FIRST CONTACTING IN THE SUBSTANTIAL ABSENCE OF WATER AN ALPHA-OLEFINIC COMPOUND OF THE FORMULA:
R,Y-PHENOL
A METHOD OF PREPARING A HYDROXY COMPOUND OF THE FORMULA: FORMULA:
WHERE R6, R7, R8 AND R9 ARE HYDROGEN OR HYDROCARBYL AND R10 IS ALKYL OF FROM 1 TO 20 CARBONS IN THE PRESENCE OF A MOLYBDENUM TUNGSTEN OR VANADIUM EPOXIDE PRODUCING CATALYST, SAID ALKANOATE PREPARED BY CONTACTING WITH OZONE A MIXTURE OF SECOND OLEFIN OF THE FORMULA:
R6R7C=CR8R9
WHERE R6, R7, R8 AND R9 ARE AS HERETOFORE DEFINED WITH AN ALKANOIC ACID OF THE FORMULA R10COOH WHERE R10 IS AS HERETOFORE DEFINED.
Abstract:
A method of producing alkanedioic acid of from 3 to 9 carbons comprising contacting in an oxidation zone a cycloalkane of from 3 to 9 carbons with a mixture comprising ozone and at least about 100 wt. percent nitric acid to form a two-phase reaction mixture containing said dioic acid and recovering said dioic acid by withdrawing said mixture to a separation zone, recycling the upper cycloalkane layer in the separation zone to the reaction zone and recovering said dioic acid from the lower layer in said separation zone, concentrating the nitric acid and byproducts in the residual lower layer for reuse in said oxidation zone.
Abstract:
A DESULFURIZATION PROCESS FOR THE REDUCTION OF SULFUR IN A SULFUR CONTAINING HYDROCARBON OIL BY CONTACTING THE SULFUR CONTAINING HYDROCARBON OIL WITH OZONE IN THE PRESENCE OF A GROUP IV-B, V-B OR GROUP VI-B METAL FOLLOWED BY SULFUR REDUCTION UTILIZING FOR EXAMPLE A BASE TREATMENT, A THERMAL TREATMENT OR A HYDROSULFURIZATION TREATMENT.
Abstract:
A METHOD OF PREPARING AN ALKANONE COMPRISING CONTACTING A SECONDARY ALKYL HALIDE WITH ALKALI METAL FLUORIDE IN THE PRESENCE OF DIMETHYL SULFOXIDE AT A TEMPERATURE LESS THAN 140*C., PREFERABLY UNDER ANHYDROUS CONDITIONS AND IN THE PRESENCE OF AN OXYGEN CONTAINING GAS.
Abstract:
A METHOD FOR PRODUCING KETONES BY CONTACTING AN N-PARAFFIN HAVING FROM 3 TO 25 CARBONS ATOMS WITH A NITRATING AGENT SELECTED FROM THE GROUP CONSISTING OF N2O3 AND A P2O5-NHO2-H2O COMBINATION IN THE PRESENCE OF AN OXYGEN CONTAINING GAS AT TEMPERATURE BETWEEN-52 AND 50*C. THE PRESENCE OF OXYGEN FUNCTIONS AS A NITRATION DIRECTOR FAVORING THE PRODUCTION OF KETONES.