Method and apparatus for producing dicyanobenzene
US-9822062-B2 · Nov 21, 2017 · US
US9868699B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9868699-B2 |
| Application number | US-201615075976-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 21, 2016 |
| Priority date | Mar 19, 2015 |
| Publication date | Jan 16, 2018 |
| Grant date | Jan 16, 2018 |
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Cations are removed from a substance stream that is produced during the production of isophoronenitrile with the help of a cation exchanger.
Opening claim text (preview).
The invention claimed is: 1. A process for removing a cation from an isophoronenitrile product mixture, said process comprising: exchanging a cation other than hydrogen in said isophoronenitrile product mixture with a hydrogen cation, to obtain a purified product; wherein said isophoronenitrile product mixture is from the preparation of isophoronenitrile from isophorone and hydrocyanic acid in the presence of a cation-containing catalyst in homogeneous phase in a reactor; wherein said cation is from the cation-containing catalyst; wherein said exchanging of the cation of the catalyst takes place by a cation exchanger without prior neutralization of the catalyst. 2. The process according to claim 1 , wherein the exchanging of the cation takes place in a cation exchanger apparatus which is designed to be single-stage or multi-stage. 3. The process according to claim 1 , wherein the exchanging of the cation takes place in a single-stage in only one cation exchanger apparatus. 4. The process according to claim 1 , wherein said cation exchanger is an immobilized cation exchanger which has, as a functional group, a sulfonic acid group which has been applied to a polystyrene matrix crosslinked with divinylbenzene. 5. The process according to claim 1 , wherein the exchanging of the cation of the catalyst takes place without neutralization of the catalyst, as first purification step after the reactor. 6. The process according to claim 2 , wherein a further work-up of the substance mixture takes place after the cation exchange apparatus by removal of a low boiler in a first column downstream of the cation exchanger, and in a second downstream column the purification of the isophoronenitrile is then carried out. 7. The process according to claim 2 , wherein a further purification of the isophoronenitrile after the cation exchange apparatus is carried out in a downstream column which contains a partial condenser placed on top or within the column. 8. The process according to claim 1 , wherein the catalyst is a soluble catalyst selected from the group consisting of a basic alkali metal compound, a basic alkaline earth metal compound and mixtures thereof; wherein the catalyst is soluble in a solvent over which the reactants react to give the product isophoronenitrile. 9. The process according to claim 1 , wherein the catalyst is an alkali metal alcoholate. 10. The process according to claim 1 , wherein the catalyst is a 20-35% strength by weight sodium methanolate solution, dissolved in methanol. 11. The process according to claim 1 , wherein the preparation of isophoronenitrile is carried out in the presence of an inert solvent. 12. The process according to claim 1 , wherein a molar ratio isophorone/HCN is 19:1 to 1.5:1. 13. The process according to claim 1 , wherein a catalyst concentration, based on the amount of isophorone used, is in the range from 0.03 to 20% by weight. 14. The process according to claim 1 , wherein the preparation of isophoronenitrile is carried out in a stirred-tank, a stirred-tank cascade, a circulation reactor, a flow tube, one or more fixed-bed reactors or a column. 15. The process according to claim 6 , wherein a low boiler is methanol. 16. The process according to claim 6 , wherein a low boiler is selected from the group consisting of methanol, isophorone, water, HCN and mixtures thereof. 17. The process according to claim 1 , wherein the catalyst is sodium methanolate. 18. The process according to claim 1 , wherein the preparation of isophoronenitrile is carried out in the absence of an inert solvent.
the ring being unsaturated · CPC title
Separation; Purification · CPC title
Alkoxylates · CPC title
using columns or beds of different ion exchange materials in series · CPC title
Recycling of catalysts · CPC title
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