IP Library Granted Patent US 12,296,301
Granted Patent B2
US 12,296,301 · App. 17/549,256 · Granted May 13, 2025

Variable, self-regulating permeate recycling in organophilic nanofiltration

Inventors: Thomas Quell (Antwerp, BE); Johannes Knossalla (Gahlen, DE); Robert Franke (Marl, DE); Stefan Drees (Dülmen, DE); Frederik Gluth (Mülheim an der Ruhr, DE); Marc Schäpertöns (Recklinghausen, DE); Fabian Höckelmann (Marl, DE)
Assignee: Evonik Oxeno GmbH & Co. KG
B01D61/08B01D61/027B01D61/10B01D61/12B01J31/4061B01D61/02B01D2311/06B01D2311/10B01D2311/14B01D2311/16B01D2311/2512B01D2313/19B01D2313/501
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Quick Facts
Patent No.
US 12,296,301
App. No.
17/549,256
Granted
May 13, 2025
Kind
B2
Abstract

The invention provides an improvement in terms of control and process technology for a method of continuous removal of a component from a liquid mixture using a membrane unit comprising at least one membrane stage. The improvement is that at least some of the overall permeate stream obtained is recycled to the feed vessel and/or beyond the feed vessel but upstream of the conveying device. The presently disclosed method can especially be used for separation of a homogeneously dissolved catalyst from a liquid reaction mixture.

Claims (28)

1. A method of continuously separating a component from a liquid mixture using a membrane unit which comprises at least one membrane stage and is fed with the mixture as feed,

wherein a membrane stage comprises at least of a conveying device, one or more membrane module(s) and a feed vessel upstream of the conveying device, and

wherein the mixture is guided from the feed vessel by means of the conveying device as feed to the one or more membrane modules, which results in reduction of the component to be separated off, based in each case on the mixture guided to the respective membrane module, in the resulting permeate stream from this respective membrane module and enrichment in the resulting retentate stream from this respective membrane module or vice versa,

wherein the overall permeate stream obtained from the last membrane stage is divided and a portion of the overall permeate stream, the recycled permeate, is recycled to the feed vessel and/or beyond the feed vessel but upstream of the conveying device and the other portion of the overall permeate stream, the permeate removed, is conducted out of the last membrane stage and out of the membrane unit on the permeate side,

wherein the recycling of the recycled permeate to the feed vessel and/or beyond the feed vessel but upstream of the conveying device is effected not by means of a conveying device but by hydraulic means, that is, by means of a pressure differential that exists between the permeate side of the membrane unit and the suction side of the conveying device or the feed vessel; and

wherein the component is a homogeneous catalyst which is separated from a reaction mixture.

2. The method according to claim 1 , wherein the mass flow rate of one of the three streams selected from feed to the membrane unit, the permeate removed, and the retentate from the membrane unit is applied to a preceding or downstream process step, and one further stream of the three is controlled toward a target value.

3. The method according to claim 1 , wherein the mass flow rate of the permeate recycled can fluctuate and is established depending on the mass flow rate of the permeate removed.

4. The method according to claim 1 , wherein the pressure on the retentate side and/or the pressure on the permeate side or the resulting transmembrane pressure and optionally the membrane module temperature are controlled in order to obtain a desired amount of the overall permeate stream.

5. The method according to claim 1 , wherein both the mass flow rate of the permeate removed and the permeate pressure are controlled by means of an adjustable flow resistor.

6. The method according to claim 1 , wherein the mass flow rate of the permeate removed, depending directly or indirectly on the fill level of the feed vessel, is subject to continuous closed-loop control, a feature of which is that—based on a target value fixed beforehand for the fill level of the feed vessel—the mass flow rate of the permeate removed increases with rising fill level of the feed vessel and the mass flow rate of the permeate removed decreases with falling fill level of the feed vessel.

7. The method according to claim 1 , wherein the pressure on the retentate side is controlled by means of the conveying device with which the feed is fed to the one or more membrane modules, and optionally a further actuator.

8. The method according to claim 1 , wherein the mass flow rate on the retentate side is controlled by means of a closed-loop mass flow controller on the retentate side comprising at least a mass flow meter and an adjustable flow resistor.

9. The method according to claim 1 , wherein the conveying device is a pump.

10. A method of continuously separating a homogeneous catalyst from a liquid reaction mixture using a membrane unit which comprises at least one membrane stage and is fed with the reaction mixture containing the homogeneous catalyst and coming from a reaction zone as feed,

wherein a membrane stage consists at least of a conveying device, one or more membrane module(s) and a feed vessel upstream of the conveying device, and

wherein the reaction mixture is guided from the feed vessel by means of the conveying device as feed to the one or more membrane modules, which results in reduction of the homogeneous catalyst, based in each case on the reaction mixture guided to the respective membrane module, in the resulting permeate stream and enrichment in the resulting retentate stream, wherein

the overall permeate stream obtained is divided and a portion of the overall permeate stream, the recycled permeate, is recycled to the feed vessel and/or beyond the feed vessel but upstream of the conveying device and the other portion of the overall permeate stream, the permeate removed, is conducted out of the at least one membrane stage and out of the membrane unit on the permeate side.

11. The method according to claim 10 , wherein the reaction mixture is taken from a reaction zone in which a homogeneously catalyzed reaction is being conducted.

12. The method according to claim 11 , wherein the homogeneously catalyzed reaction is selected from the group of the following reactions: an oxidation, an epoxidation, a hydroformylation, a hydroamination, a hydroaminomethylation, a hydrocyanation, a hydrocarboxylation, a hydrocarbonylation, a hydrocarboxyalkylation, an alkoxycarbonylation, an amination, an ammoxidation, an oximation, a hydrosilylation, an ethoxylation, a propoxylation, a carbonylation, a telomerization, a metathese, a Suzuki coupling and a hydrogenation.

13. The method according to claim 12 , wherein the homogeneously catalyzed reaction is a hydroformylation.

14. The method according to claim 2 , wherein the mass flow rate of the permeate recycled can fluctuate and is established depending on the mass flow rate of the permeate removed.

15. The method according to claim 2 , wherein the pressure on the retentate side and/or the pressure on the permeate side or the resulting transmembrane pressure and optionally the membrane module temperature are controlled in order to obtain a desired amount of the overall permeate stream.

16. The method according to claim 2 , wherein both the mass flow rate of the permeate removed and the permeate pressure are controlled by means of an adjustable flow resistor.

17. The method according to claim 2 , wherein the mass flow rate of the permeate removed, depending directly or indirectly on the fill level of the feed vessel, is subject to continuous closed-loop control, a feature of which is that—based on a target value fixed beforehand for the fill level of the feed vessel—the mass flow rate of the permeate removed increases with rising fill level of the feed vessel and the mass flow rate of the permeate removed decreases with falling fill level of the feed vessel.

18. The method according to claim 1 , wherein the pressure on the retentate side is controlled by means of the conveying device with which the feed is fed to the one or more membrane modules, and optionally a further actuator of a supply pressure regulator, or by means of a combination of a manometer and a valve on the retentate side.

19. The method according to claim 1 , wherein the mass flow rate on the retentate side, retentate mass flow rate, is controlled by means of a closed-loop mass flow controller on the retentate side comprising at least a mass flow meter and a combination of mass flow meter and conveying device.

20. The method according to claim 1 , wherein said homogenous catalyst is a transition metal catalyst.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 19, 2023
From: EVONIK OPERATIONS GMBH
To: EVONIK OXENO GMBH & CO. KG
Reel/Frame 065692/0785 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 15, 2022
From: QUELL, THOMAS; KNOSSALLA, JOHANNES; FRANKE, ROBERT; DREES, STEFAN; GLUTH, FREDERIK; SCHÄPERTÖNS, MARC; HÖCKELMANN, FABIAN
To: EVONIK OPERATIONS GMBH
Reel/Frame 060671/0915 →
Priority Claims (1)
EP 20216292 · Dec 22, 2020 · regional
Continuity (1)
Related Publication 20220193609A1 · Jun 23, 2022
References Cited (30)
US 10017443B2 · Ueken et al. · 2018 [cited by applicant]
US 10087349B2 · Brenner et al. · 2018 [cited by applicant]
US 10155200B2 · Geilen et al. · 2018 [cited by applicant]
US 10501392B2 · Fridag et al. · 2019 [cited by applicant]
US 10633302B2 · Nadolny et al. · 2020 [cited by applicant]
US 10647650B2 · Hecht et al. · 2020 [cited by applicant]
US 10654784B2 · Hasselberg et al. · 2020 [cited by applicant]
US 10850261B2 · Nadolny et al. · 2020 [cited by applicant]
US 10882027B2 · Nadolny et al. · 2021 [cited by applicant]
US 11008275B2 · Kucmierczyk et al. · 2021 [cited by applicant]
US 20060237361A1 · Dudziak et al. · 2006 [cited by applicant]
US 20160082393A1 · Priske et al. · 2016 [cited by applicant]
US 20160236150A1 · Geilen · 2016 [cited by examiner]
US 20190283004A1 · Nadolny et al. · 2019 [cited by applicant]
US 20200391194A1 · Kucmierczyk et al. · 2020 [cited by applicant]
US 20200392057A1 · Kucmierczyk et al. · 2020 [cited by applicant]
US 20200392064A1 · Kucmierczyk et al. · 2020 [cited by applicant]
US 20210179534A1 · Schulz et al. · 2021 [cited by applicant]
DE 102013113641A1 · 2015 [cited by applicant]
EP 0781166B1 · 2000 [cited by applicant]
EP 1603663B1 · 2010 [cited by applicant]
EP 3059005A1 · 2016 [cited by applicant]
WO 2014000113A1 · 2014 [cited by applicant]
WO 2014131623A1 · 2014 [cited by applicant]
WO 2014183952A1 · 2014 [cited by applicant]
WO 2020080008 · 2020 [cited by applicant]
Brächer et al., U.S. Appl. No. 17/371,477, filed Jul. 9, 2021. [cited by applicant]
Gluth et al., U.S. Appl. No. 17/549,709, filed Dec. 13, 2021. [cited by applicant]
European Search Report mailed on Jun. 17, 2021 in EP 20216292.1 (10 pages). [cited by applicant]
European Search Report received for European Patent Application No. 21214850.6, mailed on Aug. 12, 2024, 4 pages. [cited by applicant]