C07C15/085

Modified graphene, method of producing modified graphene, modified graphene-resin composite, modified graphene sheet, and modified graphene dispersion

The modified graphene includes a structure represented by the following formula (I), wherein the modified graphene has a ratio (g/d) of an intensity “g” of a G band to an intensity “d” of a D band of 1.0 or more in a Raman spectroscopy spectrum thereof:
Gr1-Ar1-X1-(Y1).sub.n1  (I)
in the formula (I), Gr1 represents a single-layer graphene or a multilayer graphene, Ar1 represents an arylene group having 6 to 18 carbon atoms, X1 represents a single bond, a linear, branched, or cyclic alkylene group having 1 to 20 carbon atoms, or a group obtained by substituting at least one carbon atom in a linear, branched, or cyclic alkylene group having 1 to 20 carbon atoms with at least one structure selected from the group consisting of —O—, —NH—, ##STR00001##
—CO—, —COO—, —CONH—, and an arylene group.

Modified graphene, method of producing modified graphene, modified graphene-resin composite, modified graphene sheet, and modified graphene dispersion

The modified graphene includes a structure represented by the following formula (I), wherein the modified graphene has a ratio (g/d) of an intensity “g” of a G band to an intensity “d” of a D band of 1.0 or more in a Raman spectroscopy spectrum thereof:
Gr1-Ar1-X1-(Y1).sub.n1  (I)
in the formula (I), Gr1 represents a single-layer graphene or a multilayer graphene, Ar1 represents an arylene group having 6 to 18 carbon atoms, X1 represents a single bond, a linear, branched, or cyclic alkylene group having 1 to 20 carbon atoms, or a group obtained by substituting at least one carbon atom in a linear, branched, or cyclic alkylene group having 1 to 20 carbon atoms with at least one structure selected from the group consisting of —O—, —NH—, ##STR00001##
—CO—, —COO—, —CONH—, and an arylene group.

Production of Alkylaromatic Compounds

A process for producing a monoalkylated benzene comprises the step of contacting benzene with a mixture comprising dialkylated and trialkylated benzenes in the presence of a transalkylation catalyst composition under transalkylation conditions effective to convert at least part of the dialkylated and trialkylated benzene to monoalkylated benzene, wherein the transalkylation catalyst, composition comprises zeolite beta having an external surface in excess of 350 m2/g as determined by the t-plot method for nitrogen physisorption.

Production of Alkylaromatic Compounds

A process for producing a monoalkylated benzene comprises the step of contacting benzene with a mixture comprising dialkylated and trialkylated benzenes in the presence of a transalkylation catalyst composition under transalkylation conditions effective to convert at least part of the dialkylated and trialkylated benzene to monoalkylated benzene, wherein the transalkylation catalyst, composition comprises zeolite beta having an external surface in excess of 350 m2/g as determined by the t-plot method for nitrogen physisorption.

METHOD FOR PRODUCING CUMENE

A method for producing cumene involves subjecting cumyl alcohol to (a) hydrocracking reaction, or (b) dehydration and subsequent hydrogenation reaction, to obtain cumene. The method includes the following steps:

(A): feeding a liquid containing cumene to a reactor loaded with a catalyst,

(B): feeding hydrogen and a liquid containing cumyl alcohol to the reactor after the step (A).

METHOD FOR PRODUCING CUMENE

A method for producing cumene involves subjecting cumyl alcohol to (a) hydrocracking reaction, or (b) dehydration and subsequent hydrogenation reaction, to obtain cumene. The method includes the following steps:

(A): feeding a liquid containing cumene to a reactor loaded with a catalyst,

(B): feeding hydrogen and a liquid containing cumyl alcohol to the reactor after the step (A).

Production of Alkylaromatic Compounds

A process for producing a monoalkylated benzene comprises contacting benzene with a mixture comprising dialkylated and trialkylated benzenes in the presence of a transalkylation catalyst composition under transalkylation conditions effective to convert at least part of the dialkylated and trialkylated benzene to monoalkylated benzene, wherein the catalyst composition comprises a metallosilicate zeolite comprising openings defined by 14-membered rings of tetrahedrally coordinated atoms and the transalkylation conditions include a temperature in the range of 160° C. to 220° C.

Production of Alkylaromatic Compounds

A process for producing a monoalkylated benzene comprises contacting benzene with a mixture comprising dialkylated and trialkylated benzenes in the presence of a transalkylation catalyst composition under transalkylation conditions effective to convert at least part of the dialkylated and trialkylated benzene to monoalkylated benzene, wherein the catalyst composition comprises a metallosilicate zeolite comprising openings defined by 14-membered rings of tetrahedrally coordinated atoms and the transalkylation conditions include a temperature in the range of 160° C. to 220° C.

PROCESS FOR TREATING POLYALKYLAROMATIC HYDROCARBONS
20220332664 · 2022-10-20 ·

A process for treating mixtures containing polyalkylaromatic hydrocarbons, intended for transalkylation processes, includes a mild reduction with hydrogen in the presence of a suitable hydrogenation catalyst. The process also relates to a transalkylation process of polyalkylaromatic hydrocarbons having the treatment.

PROCESS FOR TREATING POLYALKYLAROMATIC HYDROCARBONS
20220332664 · 2022-10-20 ·

A process for treating mixtures containing polyalkylaromatic hydrocarbons, intended for transalkylation processes, includes a mild reduction with hydrogen in the presence of a suitable hydrogenation catalyst. The process also relates to a transalkylation process of polyalkylaromatic hydrocarbons having the treatment.