Pregeneration of tetrahydroanthraquinones in a make-up solution to be added to a hydrogen peroxide working solution

Claim 2

In a process for producing hydrogen peroxide by the cyclic steps of reducing, oxidizing, and extracting a working solution containing as a working compound an alkylated anthraquinone and the corresponding hydroquinone, tetrahydroanthraquinone and tetrahydroanthrahydroquinone, the improvement which comprises increasing the mol ratio of the nuclearly-hydrogenated, tetrahydro components of the working compound in a first solution which is to be added to the working solution by adjusting the concentration of the non-nuclearly hydrogenated working compounds to be not greater than the maximum solubility of the alkylated anthrahydroquinone formed in the first solution at the hydrogenation temperature, hydrogenating the first solution in the presence of a palladium catalyst at a pressure of 50 to 400 kilopascals at a temperature of not greater than 50° C. thereby increasing the mol ratio of the tetrahydro components of the working compound without forming substantial quantities of undesirable by-products and adding said hydrogenated first solution to the working solution.

Claim 3

The process of claim 1 wherein the alkylated anthraquinone is selected from the group consisting of 2-ethylanthraquinone, 2-isobutylanthraquinone, and 2-amylanthraquinone.

Claim 4

The process of claim 1 wherein the pressure is between 100 and 200 kilopascals.

Claim 5

The process of claim 1 wherein the hydrogenation temperature is between 40° C. and 50° C.

Claim 6

The process of claim 3 wherein the alkylated anthraquinone is selected from the group consisting of 2-ethylanthraquinone, 2-isobutylanthraquinone, and 2-amylanthraquinone.

Claim 7

The process of claim 4 wherein the alkylated anthraquinone is selected from the group consisting of 2-ethylanthraquinone, 2-isobutylanthraquinone, and 2-amylanthraquinone.

Claim 8

The process of claim 1 wherein at least 90% of the hydrogenated first solution is recycled to the hydrogenator.

Claim 9

The process of claim 7 wherein the alkylated anthraquinone is selected from the group consisting of 2-ethylanthraquinone, 2-isobutylanthraquinone, and 2-amylanthraquinone.

Claim 10

The process of claim 7 wherein the pressure is between 100 and 200 kilopascals.

Claim 11

The process of claim 7 wherein the hydrogenation temperature is between 40° C. and 50° C.

Claim 12

The process of claim 9 wherein the alkylated anthraquinone is selected from the group consisting of 2-ethylanthraquinone, 2-isobutylanthraquinone, and 2-amylanthraquinone.

Claim 13

The process of claim 10 wherein the pressure is between 100 and 200 kilopascals.

Claim 14

In a process for producing hydrogen peroxide by the cyclic steps of reducing, oxidizing, and extracting a working solution containing as a working compound, one or more compounds selected from the group consisting of 2-ethylanthraquinone, 2-isobutylanthraquinone, 2-amylanthraquinone, the corresponding 2-alkylanthrahydroquinone, the corresponding 5,6,7,8-tetrahydro-2-alkylanthraquinone and the corresponding 5,6,7,8-tetrahydro-2-alkylanthrahydroquinone, the improvement which comprises increasing the mol ratio of the nuclearly-hydrogenated, tetrahydro components in a first solution which is to be added as make-up to the working solution by adjusting the concentration of the non-nuclearly hydrogenated working compounds to be not greater than the maximum solubility of the alkylated anthrahydroquinone formed in the first solution at the hydrogenation temperature, hydrogenating the first solution at a pressure of 100 to 400 kilopascals, at a temperature of 40° C. to 50° C., recycling at least 90% of the working solution to the hydrogenator without oxidation and extraction thereby increasing the mol ratio of the tetrahydro components of the working compound without forming substantial quantities of undesired by-products and adding the first solution as make-up to the working solution.

Claim 15

In a process for producing hydrogen peroxide by the cyclic steps of reducing, oxidizing, and extracting a working solution containing as a working compound, one or more compounds selected from the group consisting of 2-ethylanthraquinone, 2-isobutylanthraquinone, 2-amylanthraquinone, the corresponding 2-alkylanthrahydroquinone, the corresponding 5,6,7,8-tetrahydro-2-alkylanthraquinone and the corresponding 5,6,7,8-tetrahydro-2-alkylanthrahydroquinone, the improvement which comprises increasing the mol ratio of the nuclearly-hydrogenated, tetrahydro components in a first solution which is to be added as make-up to the working solution by adjusting the concentration of the non-nuclearly hydrogenated working compounds to be not greater than the maximum solubility of the alkylated anthrahydroquinone formed in the first solution at the hydrogenation temperature, hydrogenating the first solution at a pressure of 100 to 400 kilopascals, at a temperature of 40° C. to 50° C., recycling at least 90% of the working solution to the hydrogenator without oxidation and extraction thereby increasing the mol ratio of the tetrahydro components of the working compound without forming substantial quantities of undesired by-products and adding the first solution as make-up to the working solution.

Claim 16

The process of claim 13 wherein the first solution comprises working solution withdrawn from the plant process stream.

Claim 17

The process of claim 13 wherein the adjusting step is repeated at least once after the hydrogenation step.

Claim 18

The process of claim 14 wherein the hydrogenation pressure is 100 to 200 kilopascals.

Claim 19

The process of claim 15 wherein the hydrogenation pressure is 100 to 200 kilopascals.

Claim 20

In a process for producing hydrogen peroxide by the cyclic steps of reducing, oxidizing, and extracting a working solution containing as a working compound, one or more compounds selected from the group consisting of 2-ethylanthraquinone, 2-isobutylanthraquinone, 2-amylanthraquinone, the corresponding 2-alkylanthrahydroquinone, the corresponding 5,6,7,8-tetrahydro-2-alkylanthraquinone and the corresponding 5,6,7,8-tetrahydro-2-alkylanthrahydroquinone, the improvement which comprises hydrogenating a first solution containing a working compound and an inert solvent in a sidestream hydrogenator at a pressure of 100 to 400 kilopascals, at a temperature of not greater than 50° C. to increase the mol ratio of the nuclearly-hydrogenated, tetrahydro components in the first solution, adding up to 10% of the first solution from the sidestream hydrogenator as make-up to the working solution, recycling at least a part of the first solution as make-up to the sidestream hydrogenator without oxidation and extraction thereby further increasing the mol ratio of the tetrahydro components of the working compound without forming substantial quantities of undesired by-products, adjusting the concentration of the non-nuclearly hydrogenated working compounds in the first solution to be no greater than the maximum solubility of the alkylated anthraquinone formed in the first solution at the hydrogenation temperature, and concomitantly replacing the portion of the first solution added as make-up to the working solution with additional solvent and working compound.

Claim 21

In a process for producing hydrogen peroxide by the cyclic steps of reducing, oxidizing, and extracting a working solution containing as a working compound, one or more compounds selected from the group consisting of 2-ethylanthraquinone, 2-isobutylanthraquinone, 2-amylanthraquinone, the corresponding 2-alkylanthrahydroquinone, the corresponding 5,6,7,8-tetrahydro-2-alkylanthraquinone and the corresponding 5,6,7,8-tetrahydro-2-alkylanthrahydroquinone, the improvement which comprises hydrogenating a first solution containing a working compound and an inert solvent in a sidestream hydrogenator at a pressure of 100 to 400 kilopascals, at a temperature of not greater than 50° C. to increase the mol ratio of the nuclearly-hydrogenated, tetrahydro components in the first solution, adding up to 10% of the first solution from the sidestream hydrogenator as make-up to the working solution, recycling at least a part of the first solution as make-up to the sidestream hydrogenator without oxidation and extraction thereby further increasing the mol ratio of the tetrahydro components of the working compound without forming substantial quantities of undesired by-products, adjusting the concentration of the non-nuclearly hydrogenated working compounds in the first solution to be no greater than the maximum solubility of the alkylated anthraquinone formed in the first solution at the hydrogenation temperature, and concomitantly replacing the portion of the first solution added as make-up to the working solution with additional solvent and working compound.

Claim 22

The process of claim 18 wherein the additional solvent comprises working solution withdrawn from the plant process stream.

Claim 23

The process of claim 18 wherein the adjusting step is repeated at least once after the hydrogenation step.

Claim 24

The process of claim 19 wherein the hydrogenation pressure is 100 to 200 kilopascals and the hydrogenation temperature is 40° C. to 50° C.

Claim 25

The process of claim 19 wherein the hydrogenation pressure is 100 to 200 kilopascals and the hydrogenation temperature is 40° C. to 50° C.

Claim 26

The process of claim 20 wherein the hydrogenation pressure is 100 to 200 kilopascals and the hydrogenation temperature is 40° C. to 50° C.