Separation of 6-aminocapronitrile and hexamethylenediamine from a mixture comprising hexamethylenediamine, 6-aminocapronitrile and tetrahydroazepine
View Patent ↗The invention relates to the field of separation by distillation of 6-aminocapronitrile (ACN) and hexamethylenediamine (HMD) from a mixture comprising ACN, HMD, tetrahydroazepine (THA), adiponitrile (ADN) and low boilers (LB). Also disclosed is a method for producing a distillate stream comprising HMD; a side draw stream comprising ACN, THA and low levels of dimers of ACN and HMD; and a tails stream comprising ACN, THA and substantially higher levels of dimers of ACN and HMD than found in the side draw stream. The side draw stream is particularly suitable for use in the production of caprolactam since the low levels of dimers of ACN and HMD do not greatly affect the catalyst life in the caprolactam production process. The tails stream can be further distilled to produce a tails distillate stream comprising ACN and THA, which can be recycled back to the first distillation column, further increasing recovery of ACN from the feed stream. Process conditions of the method of the invention disfavor the production of 2-cyanocyclopentylideneimine (CPI).
1. A method of separating a feed mixture comprising 6-aminocapronitrile (ACN) and hexamethylenediamine (HMD), comprising:
introducing a feed mixture comprising ACN, tetrahydroazepine (THA) and HMD into a refined distillation column; and
operating the refined distillation column under conditions such that:
a refined column distillate comprising HMD is withdrawn from the refined distillation column;
a refined column side draw comprising ACN, THA and low levels of dimers of ACN and HMD is withdrawn from the refined distillation column; and
a refined column tails comprising ACN, THA and high levels of dimers of ACN and HMD is withdrawn from the refined distillation column,
wherein the levels of dimers of ACN and HMD in the refined column tails substantially exceeds the level of dimers of ACN and HMD in the refined column side draw.
2. The method of claim 1 wherein the head pressure of the refined distillation column is about 200 to about 760 mm Hg absolute and the pressure drop across the refined distillation column height is about 25 to about 300 mm Hg.
3. The method of claim 2 wherein the head pressure of the refined distillation column is about 200 mm Hg absolute and the pressure drop across the refined distillation column height is greater than about 25 mm Hg.
4. The method of claim 1 further comprising:
introducing the refined column tails into a recycle distillation column; operating the recycle distillation column under conditions such that:
a recycle column distillate comprising ACN and THA is withdrawn from the recycle distillation column;
a recycle column tails comprising dimers of ACN and HMD is withdrawn from the recycle distillation column; and
introducing at least some of the recycle column distillate into the refined distillation column along with the feed mixture.
5. The method of claim 4 wherein the head pressure of the recycle distillation column is less than about 50 mm Hg absolute.
6. The method of claim 5 wherein the head pressure of the recycle distillation column is less than about 20 mm Hg absolute.
7. The method of claim 1 further comprising;
introducing an ammonia-depleted crude feed mixture comprising HMD, ACN, THA and adiponitrile (ADN) into a crude distillation column; and
operating the crude distillation column under conditions to minimize isomerization of ADN into 2-cyanocyclopentylideneimine (CPI) such that:
a crude column distillate comprising HMD, ACN and THA is withdrawn from the crude distillation column; and
a crude column tails comprising ADN, HMD, ACN and THA is withdrawn from the crude distillation column;
wherein the crude column distillate comprises the feed mixture for the refined distillation column.
8. The method of claim 7 wherein the head pressure of the crude distillation column is about 5 to about 100 mm Hg absolute.
9. The method of claim 8 wherein the head pressure of the crude distillation column is about 60 mm Hg absolute.
10. The method of claim 7 further comprising:
introducing the crude column tails into a tails distillation column; operating the tails distillation column under conditions such that:
a tails column distillate comprising HMD, ACN and THA is withdrawn from the tails distillation column; and
a tails column tails comprising ADN and CPI is withdrawn from the tails distillation column; and
reintroducing the tails column distillate into the crude distillation column.
11. The method of claim 10 wherein the head pressure of the tails distillation column is about 10 to about 60 mm Hg absolute.
12. The method of claim 11 wherein the head pressure of the tails distillation column is about 20 mm Hg absolute.