IP Library Granted Patent US 9,284,256
Granted Patent B2
US 9,284,256 · App. 14/415,794 · Granted Mar 15, 2016

Process for the production of nitrobenzene by adiabatic nitration

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Quick Facts
Patent No.
US 9,284,256
App. No.
14/415,794
Granted
Mar 15, 2016
Kind
B2
Abstract

The present invention provides a continuous process for the production of nitrobenzene by nitration of benzene with mixtures of sulfuric and nitric acid using a stoichiometric excess of benzene, in which the content of aliphatic organic compounds in the feed benzene during the start-up period of the production plant is always maintained at less than 1.5 wt. %, based on the total mass of the feed benzene. This is achieved either by mixing the feed benzene comprising recycled unreacted benzene (recycled benzene) and benzene newly supplied to the reaction (fresh benzene) in appropriate quantitative ratios during the start-up period, depending on the purity of the two streams, or by completely omitting the recycling of unreacted benzene during the start-up period, i.e. the feed benzene consists only of benzene newly supplied to the reaction.

Claims (22)

1. A continuous process for the production of nitrobenzene by nitration of benzene, comprising:

a) reacting a benzene-comprising stream (a.1), which comprises at least 90 wt. % benzene, based on the total mass of (a.1), in a reactor with a mixture of sulfuric acid (a.2) and nitric acid (a.3) under adiabatic conditions, wherein benzene is used in a stoichiometric excess based on nitric acid (a.3), wherein the quantity M′ of the benzene-comprising stream (a.1) supplied to the reactor per hour is increased within a period from the beginning of the nitration until a preset target value for M′ is reached,

b) separating the process product obtained in step a) into an aqueous phase comprising sulfuric acid (b.1) and an organic phase comprising nitrobenzene (b.2),

c) concentrating the aqueous phase (b.1) obtained in step b) by evaporation of water to form an aqueous phase (c.1) with an increased sulfuric acid concentration compared with (b.1), wherein the phase (c.1) is partially to completely returned into step a) and used as a component of (a.2), and

d) working up the organic phase (b.2) obtained in step b) to form pure nitrobenzene (d.1), wherein a benzene-comprising stream (d.2) is obtained, wherein the stream (d.2) is partially to completely returned into step a) and used as a component of (a.1), the recirculation of (d.2) already taking place during the period t,

wherein

at least during the period t only a benzene-comprising stream (a.1) having a content of aliphatic organic compounds of less than 1.5 wt. %, based on the total mass of (a.1), is supplied to the reactor.

2. A continuous process for the production of nitrobenzene by nitration of benzene, comprising:

a) reacting a benzene-comprising stream (a.1), which comprises at least 90 wt. % benzene, based on the total mass of (a.1), in a reactor with a mixture of sulfuric acid (a.2) and nitric acid (a.3) under adiabatic conditions, wherein benzene is used in a stoichiometric excess based on nitric acid (a.3), wherein the quantity M′ of the benzene-comprising stream (a.1) supplied to the reactor per hour is increased within a period from the beginning of the nitration until a preset target value for M′ is reached,

b) separating the process product obtained in step a) into an aqueous phase comprising sulfuric acid (b.1) and an organic phase comprising nitrobenzene (b.2),

c) concentrating the aqueous phase (b.1) obtained in step b) by evaporation of water to form an aqueous phase (c.1) with an increased sulfuric acid concentration compared with (b.1), wherein the phase (c.1) is partially to completely returned into step a) and used as a component of (a.2), and

d) working up the organic phase (b.2) obtained in step b) to form pure nitrobenzene (d.1), wherein a benzene-comprising stream (d.2) is obtained,

wherein

at least during the period t only a benzene-comprising stream (a.1) having a content of aliphatic organic compounds of less than 1.5 wt. %, based on the total mass of (a.1), is supplied to the reactor and that only after the period t has passed is the benzene-comprising stream (d.2) obtained in step d) partially to completely returned into step a) and used as a component of (a.1).

3. The process according to claim 1 , in which the aliphatic organic compounds are selected from the group consisting of cyclohexane, heptane, methylcyclohexane, bicycloheptane, isomers of dimethylcyclopentane, ethylcyclopentane, pentane, cyclopentane and 2-methylhexane.

4. The process according to claim 1 , in which at least 25 wt. % of the stream (d.2) is always returned into step a).

5. The process according to claim 1 , in which benzene is used in step a) in an excess of 2.0% to 20% of the theoretical value.

6. The process according to claim 1 , in which the benzene-comprising stream (d.2) encompasses 40.0 wt. % to 99.9 wt. % benzene, based on the total mass of (d.2).

7. The process according to claim 2 , in which the aliphatic organic compounds are selected from the group consisting of cyclohexane, heptane, methylcyclohexane, bicycloheptane, isomers of dimethylcyclopentane, ethylcyclopentane, pentane, cyclopentane and 2-methylhexane.

8. The process according to claim 3 , in which at least 25 wt. % of the stream (d.2) is always returned into step a).

9. The process according to claim 2 , in which benzene is used in step a) in an excess of 2.0% to 20% of the theoretical value.

10. The process according to claim 2 , in which the benzene-comprising stream (d.2) encompasses 40.0 wt. % to 99.9 wt. % benzene, based on the total mass of (d.2).

Assignments (2)
CHANGE OF NAME Recorded Apr 5, 2016
From: BAYER MATERIALSCIENCE AG
To: COVESTRO DEUTSCHLAND AG
Reel/Frame 038358/0387 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 4, 2015
From: KNAUF, THOMAS; MERKEL, MICHAEL
To: BAYER MATERIALSCIENCE AG
Reel/Frame 034881/0776 →