METHOD FOR PURIFYING PHOSPHORIC ACID

Abstract

The present invention relates to a method for purifying phosphoric acid from a mixture which comprises organic compounds and water. In particular the present invention relates to a method for purifying phosphoric acid from a a pulping slurry, containing or consisting of phosphoric acid, one or more organic compounds and water, comprising or consisting of the following steps: i) providing a mixture containing or consisting of phosphoric acid, one or more substance(s) S having at least one secondary carbon atom attached to an alkoxy group, one or more (further) organic compounds and water, and adjusting (if necessary) the molar ratio of phosphoric acid to the total of one or more substance(s) S, having at least one secondary carbon atom attached to an alkoxy group, in the mixture to be in the range of from 1:0.4 to 1:10, preferably to be in the range of approximately 1:0.6 to 1:4, especially preferably to be approximately 1:0.85 to 1:2, ii) heating the mixture to 25 C. or more until phase separation occurs, iii) removing the light phase, and iv) separating the phosphoric acid from the heavy phase.

Claims

1. A method for purifying phosphoric acid from a mixture comprising phosphoric acid, one or more organic compounds, and water, the method comprising: i) providing a mixture comprising phosphoric acid, one or more substance(s) S having at least one secondary carbon atom attached to an alkoxy group, one or more (further) organic compounds, and water, and adjusting the molar ratio of phosphoric acid to the total of the one or more substance(s) S, having at least one secondary carbon atom attached to an alkoxy group, in the mixture to be in the range of from 1:0.4 to 1:10, ii) heating the mixture to 25 C. or more until phase separation occurs, iii) removing a light phase, and iv) separating the phosphoric acid from a heavy phase.

2. The method according to claim 1, wherein the separation of step iv) is conducted by distillation or extraction.

3. The method according to claim 1, further comprising: v) separating the one or more substance(s) S from the heavy phase obtained in iv).

4. The method according to claim 3, wherein the one or more substance(s) S obtained in v) is reused in step i).

5. The method according to claim 1, wherein the mixture provided in i) contains CO.sub.2.

6. The method according to claim 1, wherein the one or more (further) organic compounds is/are selected from the group consisting of hydrocarbons, alcohols, aldehydes, ketones, acids, esters, ethers, carbohydrates, amino acids and derivates thereof as well as di-, tri-, oligo- or polymers thereof.

7. The method according to claim 1, wherein the one or more (further) organic compounds is/are selected from the group consisting of organic solvents.

8. The method according to claim 7, wherein the one or more (further) organic solvent(s) has/have a miscibility gap with water.

9. The method according to claim 1, wherein the one or more (further) organic compounds is/are selected from the group consisting of polysaccharides, oligosaccharides, and hydrolysation products thereof.

10. The method according to claim 1, wherein the one or more (further) organic compounds is/are selected from the group consisting of cellulose, hemicellulose, and lignin.

11. The method according to claim 1, wherein the one or more substance(s) S is/are selected from the group consisting of methyl-isopropyl ether, ethyl-isopropyl ether, propyl-isopropyl ether, di-isopropyl ether, sec-butyl-methyl ether, sec-butyl-ethyl ether, sec-butyl-propyl ether, sec-butyl-isopropyl ether, sec-butyl-butyl ether, bis(sec-butyl) ether, sec-butyl-tert.-butyl ether, 3-methoxy-pentane, 3-ethoxy pentane, 3-propoxy pentane, 3-(1-methyl-ethoxy)-pentane, 3-butoxy-pentane, 3-(2-methyl-propoxy)-pentane, 3-(1-methyl-propoxy)-pentane, 3-(1,1-methyl-ethoxy)-pentane, 3-pentoxy-pentane, 3-(1-methyl-butoxy)-pentane, 3-(2-methyl-butoxy)-pentane, 3-(3-methyl-butoxy)-pentane, 3-(1-ethyl-propxy)-pentane, 3-(2-ethyl-propxy)-pentane, 2-methoxy-pentane, 2-ethoxy pentane, 2-propoxy pentane, 2-(1-methyl-ethoxy)-pentane, 2-butoxy-pentane, 2-(2-methyl-propoxy)-pentane, 2-(1-methyl-propoxy)-pentane, 2-(1,1-methyl-ethoxy)-pentane, 2-pentoxy-pentane, 2-(1-methyl-butoxy)-pentane, 2-(2-methyl-butoxy)-pentane, 2-(3-methyl-butoxy)-pentane, 2-(1-ethyl-propxy)-pentane, 2-(2-ethyl-propoxy)-30 pentane, 2-methoxy-3-methyl-butane, 2-ethoxy-3-methyl-butane, 2-propoxy-3-methyl-butane, 2-(1-methyl-ethoxy)-3-methyl-butane, 2-butoxy-3-methyl-butane, 2-(2-methyl-propoxy)-3-methyl-butane, 2-(1-methyl-propoxy)-3-methyl-butane, 2-(1,1-methyl-ethoxy)-3-methyl-butane, 1-(3-methyl-butoxy)-pentane, 2-(1-methyl-butoxy)-3-methyl-butane,2-(2-methyl-butoxy)-3-methyl-butane, 2-(3-methyl-butoxy)-3-methyl-butane, 2-(1-ethyl-propoxy)-3-methyl-butane, and 2-(2-ethyl-propoxy)-3-methyl-butane.

12. The method according to claim 1, wherein the one or more substance S comprises di-isopropyl ether.

13. The method according to claim 1, wherein the light phase formed in ii) contains 10 wt.-% or less phosphoric acid.

14. The method according to claim 1, wherein the mixture is heated to 30 C. or more in ii).

15. The method according to claim 1, wherein ii) is conducted under pressurized conditions and/or wherein additional water is added in ii).

16. The method according to claim 1 comprising adjusting the molar ratio of phosphoric acid to the total of the one or more substance(s) S, having at least one secondary carbon atom attached to an alkoxy group, in the mixture to be in the range of 1:0.6 to 1:4.

17. The method according to claim 1 comprising adjusting the molar ratio of phosphoric acid to the total of the one or more substance(s) S, having at least one secondary carbon atom attached to an alkoxy group, in the mixture to be in the range of approximately 1:0.85 to 1:2.

18. The method according to claim 1, wherein the mixture is heated to 40 C. or more in ii).

19. The method according to claim 1, wherein the mixture is heated to 50 C. or more in ii).

20. The method according to claim 3, wherein the one or more substance S comprises di-isopropyl ether.

Description

EXAMPLE 1

[0060] A solution of 42 g phosphoric acid (85 wt %), 30 g ethanol and 5 g saccharose was admixed with 34 g diisopropyl ether at room temperature. Instantaneously 4.7 g of a white substance crystallized and was filtered off.

[0061] Afterwards the filtrate was heated to 45 C. and a spontaneous phase separation occurred. The light, clear phase had a volume of 20 ml and a phosphoric acid content of 5 wt %. Further heating to 65 C. enlarged the light phase to 45 ml while the content of phosphoric acid was reduced to 2 wt %.

EXAMPLE 2

[0062] A solution of 42 g phosphoric acid (85 wt %), 38 g ethyl acetate und 7 g cellobiose was admixed with 46 g diisopropyl ether at room temperature. Instantaneously 6.8 g of a white substance crystallized and was filtered off.

[0063] Afterwards the filtrate was heated to 40 C. and a spontaneous phase separation occurred. The light, clear phase had a volume of 15 ml and a phosphoric acid content of 6 wt %. Further heating to 65 C. enlarged the light phase to 65 ml.

EXAMPLE 3

[0064] A solution of 42 g phosphoric acid (85 wt %), 34 g acetone und 10 g lignin was admixed with 46 g sec-butyl-isopropyl ether at room temperature. Instantaneously 6.8 g of a white substance crystallized and was filtered off.

[0065] Afterwards the filtrate was heated to 45 C. and a spontaneous phase separation occurred. The light, clear phase had a volume of 45 ml and a phosphoric acid content of 5.4 wt %.