Processes for recovery of a triarylphosphine from a group VIII metal catalyst complex mixture
View Patent ↗Processes for recovering at least one triarylphosphine from a Group VIII metal catalyst triarylphosphine complex mixture are provided. The processes are particularly useful for recovering the triarylphosphine from spent Group VIII metal catalyst complex mixtures. The processes include the steps of (i) forming a distillate from a Group VIII catalyst complex mixture containing a Group VIII metal catalyst complex, a triarylphosphine, and a light ends component wherein the distillate contains at least a portion of the triarylphosphine as a vapor and at least a portion of the light ends component as a vapor; (ii) cooling the distillate to a temperature below the boiling point of the light ends component to form a condensate; (iii) crystallizing at least a portion of the triarylphosphine using the light ends component as a crystallizing liquid; and (v) recovering the crystallized triarylphosphine from the condensate.
1. A process for recovering a triphenylphosphine from a Group VIII metal catalyst complex mixture comprising:
(i) producing a distillate from a Group VIII metal catalyst complex mixture comprising a Group VIII metal catalyst complex, a triphenylphosphine, and a light ends component wherein the distillate comprises at least a portion of the triphenylphosphine as a vapor and at least a portion of the light ends component as a vapor;
(ii) cooling the distillate to a temperature below the boiling point of the light ends component to form a condensate comprising from 70 wt. % to 95 wt. % of the light ends component in liquid form and from 5 wt. % to 30 wt. % of the triphenylphosphine;
(iii) cooling the condensate to a temperature at which at least a portion of the triphenylphosphine is converted to triphenylphosphine crystals in the condensate wherein the condensate is free of an added solvent; and
(iv) recovering at least a portion of the triphenylphosphine crystals from the condensate.
2. The process of claim 1 wherein the distillate is produced from a mixture comprising a liquid triarylphosphine obtained by heating the Group VIII metal catalyst complex mixture to a temperature above the melting point of the triarylphosphine to form a mixture comprising liquid triarylphosphine, the Group VIII metal catalyst complex, and the light ends component.
3. The process of claim 2 wherein the Group VIII metal catalyst complex is heated to a temperature of 600° C. to 200° C. to form the mixture comprising the liquid triarylphosphine.
4. The process of claim 3 wherein the distillate comprising at least a portion of the triarylphosphine as a vapor and at least a portion of the light ends component as a vapor is formed by subjecting the mixture comprising the liquid triarylphosphine to a temperature of 230° C. to 315° C. and a pressure of 0.16 kPa to 3.3 kPa.
5. The process of claim 4 wherein the condensate is formed by cooling the distillate comprising at least a portion of the triarylphosphine as a vapor and at least a portion of the light ends component as a vapor to a temperature of 50° C. to 90° C.
6. The process of claim 5 wherein the triarylphosphine is selected from the group consisting of triphenylphosphine, tri-p-tolylphosphine, tri-m-tolylphosphine, trixylyl-phosphine, tris(p-ethylphenyl)phosphine, tris(p-methoxyphenyl)phosphine, and mixtures thereof.
7. The process of claim 6 wherein the Group VIII metal catalyst is selected from the group consisting of rhodium, ruthenium, palladium, osmium, iridium, and combinations thereof.
8. The process of claim 7 wherein the triarylphosphine is triphenylphosphine and wherein the Group VIII metal catalyst metal is rhodium.
9. The process of claim 8 wherein the mixture comprising the liquid triarylphosphine comprises from 10 wt. % to 80 wt. % of the triarylphosphine and from 10 wt. % to 80 wt. % of the light ends component.
10. The process of claim 9 wherein the distillate contains from 20 wt. % to 40 wt. % of the triarylphosphine and from 60 wt. % to 90 wt. % of the light ends component.
11. The process of claim 10 wherein the condensate comprises from 70 wt. % to 95 wt. % of the light ends component in liquid form and from 5 wt. % to 30 wt. % of the triphenylphosphine.
12. The process of claim 11 wherein the distillate is formed by subjecting the mixture comprising the liquid triarylphosphine to a temperature of 240° C. to 290° C. and a pressure of 0.18 kPa to 2.3 kPa.
13. The process of claim 12 wherein the condensate is cooled to a temperature of 10° C. to 50° C. to form triarylphosphine crystals in the condensate.
14. The process of claim 8 wherein the mixture comprising the Group VIII metal catalyst triarylphosphine complex, a triarylphosphine, and a light ends component comprises a heavy ends component.
15. The process of claim 14 wherein the distillate comprises at least a portion of the heavy ends component.
16. The process of claim 14 wherein the mixture comprising the liquid triarylphosphine comprises from 20 wt. % to 80 wt. % of the liquid triarylphosphine, from 20 wt. % to 60 wt. % of the light end component; and from 20 wt. % to 50 wt. % of the heavy ends component.
17. The process of claim 11 wherein the condensate comprises from 70 wt. % to 95 wt. % of the light ends component in liquid form; from 5 wt. % to 30 wt. % of the triphenylphosphine; and from 2 wt. % to 12 wt. % of a heavy ends component.