Oligomerization of ethene in supercritical mode

Patent metadata

Field	Value
Publication number	US-10189755-B2
Application number	US-201715605170-A
Country	US
Kind code	B2
Filing date	May 25, 2017
Priority date	Jun 10, 2016
Publication date	Jan 29, 2019
Grant date	Jan 29, 2019

Abstract

The disclosure describes the oligomerization of supercritical ethene. An essential aspect of the invention is that of mixing ethene with an inert medium and setting the conditions in the reaction such that both ethene and the inert medium are supercritical. This is because the solubility for ethene in the inert medium is greater in the supercritical state, such that more ethene is dissolved in the supercritical inert medium than in a liquid solvent. The process regime in the supercritical state therefore enables the use of a much higher proportion of ethene in a homogeneous mixture of ethene and inert medium than is possible on the basis of the thermodynamic solubility restriction in a purely liquid hydrocarbon stream. In this way, the space-time yield is distinctly enhanced. Since a greater amount of ethene can be passed into the reactor, it is possible as a result to better exploit the apparatus volume compared to a liquid phase process. The inert medium used may, for example, be isobutane.

First claim

The invention claimed is:

1. A process for oligomerizing ethene, comprising:
(I) an oligomerization operation, in which a mixture comprising ethene and an inert medium contacts a solid catalyst, wherein the proportion by weight of the inert medium in the mixture is greater than the proportion by weight of ethene in the mixture, wherein the inert medium is a C 3 -C 7 alkane or a C 3 -C 7 cycloalkane, wherein the pressure and temperature of the mixture are chosen with respect to the proportion by weight of ethene in the mixture such that the ethene and the inert medium are in the supercritical state, and wherein the ethene and the inert medium each contact the solid catalyst in the supercritical state; and
(II) a regeneration operation, in which the solid catalyst in the absence of ethene, hydrogen, and oxygen is purged with a liquid purge medium, wherein:
a) operation is interchanged over time between the oligomerization operation and the regeneration operation, in such a way that a time-limited oligomerization operation is followed by a time-limited regeneration operation, and the latter in turn is followed by a time-limited oligomerization operation;
b) the solid catalyst is always at the same location during both the oligomerization operation and the regeneration operation;
c) the location of the solid catalyst is supplied with positive or negative thermal energy in order to impose a set temperature thereon during both the oligomerization operation and the regeneration operation;
d) the set temperature in the regeneration operation is lower than the set temperature in the oligomerization operation; and
e) the pressure at the location of the solid catalyst is lower in the regeneration operation than in the oligomerization operation.

2. The process according to claim 1 , wherein the mixture is at first provided in the supercritical state and then contacted with the solid catalyst, where the provision of the mixture in the supercritical state is affected either according to alternative a) or according to alternative b):
a) the inert medium is converted to the supercritical state by increasing the pressure and/or temperature of the inert medium and ethene is metered into the supercritical inert medium to obtain the supercritical mixture;
b) the inert medium and ethene are mixed to give the mixture, and the mixture is converted to the supercritical state by increasing the temperature and/or pressure of the mixture.

3. The process according to claim 1 , wherein the inert medium is selected from the group consisting of propane, isobutane, n-butane, isopentane, n-pentane, n-hexane, n-heptane, cyclopentane, cyclohexane, 2-methylpentane, 3-methylpentane, 2-methylhexane, 3-methylhexane, methylcyclopentane, or methylcyclohexane.

4. The process according to claim 3 , wherein the inert medium is isobutane, and wherein the proportion of ethene in the mixture on commencement of contact with the solid catalyst is between 4% by weight and 30% by weight, the pressure of the mixture is adjusted to a value between 25*10 5 Pa and 100*10 5 Pa, and the temperature of the mixture is adjusted to a value between 90° C. and 200° C., wherein both ethene and isobutane are in the supercritical state.

5. The process according to claim 4 , wherein the mixture is provided as a reactant mixture together with at least one accompanying substance, where the reactant mixture on commencement of contact with the solid catalyst has the following composition that adds up to 100% by weight:
Isobutane: 70% by weight to 96% by weight;
Ethene: between 4% by weight and 30% by weight;
Sum of all accompanying substances: more than 0% by weight to a maximum of 5% by weight.

6. The process according to claim 4 , wherein a product mixture having the following composition that adds up to 100% by weight is drawn off from the solid catalyst:
Isobutane: 70% by weight to 96% by weight;
Ethene: 0% by weight to 2% by weight;
Olefins having four carbon atoms: 2.3% by weight to 21% by weight;
Olefins having six carbon atoms: 0.9% by weight to 7.2% by weight;
Olefins having eight carbon atoms: 0.1% by weight to 6.3% by weight;
Olefins having ten carbon atoms: 0% by weight to 3% by weight;
Olefins having twelve carbon atoms: 0% by weight to 2.7% by weight;
Sum of all other constituents: 0% by weight to 5% by weight.

7. The process according to claim 3 , wherein the inert medium is n-hexane, wherein the proportion of ethene in the mixture on commencement of contact with the solid catalyst is between 5% by weight and 30% by weight, the pressure of the mixture is adjusted to a value between 25*10 5 Pa and 100*10 5 Pa, and the temperature of the mixture is adjusted to a value between 90° C. and 250° C., wherein both ethene and n-hexane are in the supercritical state.

8. The process according to claim 1 , wherein the solid catalyst comprises at least two components, where the first component comprises at least one element selected from Ni, Cr, Fe, or Ti which is in metallic, oxidic, or hydridic form, and where the second component comprises at least one metal oxide selected from the group consisting of Al 2 O 3 , SiO 2 , TiO 2 , and ZrO 2 .

9. The combination process according to claim 1 , wherein the liquid purge medium and the inert medium is the same substance.

10. The process according to claim 9 , wherein the liquid purge medium and the inert medium is isobutane, wherein the pressure in the oligomerization operation is adjusted to a value between 45*10 5 Pa and 55*10 5 Pa and the temperature in the oligomerization operation is adjusted to a value between 125° C. and 155° C., and wherein the pressure in the regeneration operation is adjusted to a value between 25*10 5 Pa and 35*10 5 Pa and the temperature in the regeneration operation is adjusted to a value between 105° C. and 125° C.

11. The process according to claim 2 , wherein the inert medium is one of the following substances: propane, isobutane, n-butane, isopentane, n-pentane, n-hexane, n-heptane, cyclopentane, cyclohexane, 2-methylpentane, 3-methylpentane, 2-methylhexane, 3-methylhexane, methylcyclopentane, or methylcyclohexane.

12. The process according to claim 5 , wherein a product mixture having the following composition that adds up to 100% by weight is drawn off from the solid catalyst:
Isobutane: 70% by weight to 96% by weight;
Ethene: 0% by weight to 2% by weight;
Olefins having four carbon atoms: 2.3% by weight to 21% by weight;
Olefins having six carbon atoms: 0.9% by weight to 7.2% by weight;
Olefins having eight carbon atoms: 0.1% by weight to 6.3% by weight;
Olefins having ten carbon atoms: 0% by weight to 3% by weight;
Olefins having twelve carbon atoms: 0% by weight to 2.7% by weight;
Sum of all other constituents: 0% by weight to 5% by weight.

13. The process according to claim 2 , wherein the solid catalyst comprises at least two components, where the first component comprises at least one element selected from Ni, Cr, Fe, or Ti which is in metallic, oxidic, or hydridic form, and where the second component comprises at least one metal oxide selected from the group consisting of Al 2 O 3 , SiO 2 , TiO 2 , and ZrO 2 .

14. The process according to claim 3 , wherein the solid catalyst is in the solid state and comprises at least two components, where the first component comprises at least one element selected from the group consisting of Ni, Cr, Fe, and Ti which is in metallic, oxidic, or hydridic form, and where the second component comprises at least one metal oxide selected from the group consisting of Al 2 O 3 , SiO 2 , TiO 2 , and ZrO 2 .

15. The process accordin

Assignees

• Evonik Degussa Gmbh

Inventors

• Reeker Helene
• Stochniol Guido
• Maschmeyer Dietrich
• Peitz Stephan
• Schallenberg Jörg

Classifications

• B01J21/063

  Titanium; Oxides or hydroxides thereof · CPC title

• B01J2038/005

  involving supercritical treatment · CPC title

• C07C11/107

  with six carbon atoms · CPC title

• B01J21/12

  Silica and alumina · CPC title

• B01J38/56

  Hydrocarbons · CPC title