WO1998029367A1 - Apparatus and method for separating olefins from an olefins-rich product stream - Google Patents

Apparatus and method for separating olefins from an olefins-rich product stream Download PDF

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Publication number
WO1998029367A1
WO1998029367A1 PCT/US1997/023876 US9723876W WO9829367A1 WO 1998029367 A1 WO1998029367 A1 WO 1998029367A1 US 9723876 W US9723876 W US 9723876W WO 9829367 A1 WO9829367 A1 WO 9829367A1
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WO
WIPO (PCT)
Prior art keywords
olefins
product stream
stream
group
permeate
Prior art date
Application number
PCT/US1997/023876
Other languages
English (en)
French (fr)
Inventor
Richard B. Hall
Stephen N. Vaughn
W. S. Winston Ho
Hsiang-Ning Sun
Original Assignee
Exxon Chemical Patents Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Exxon Chemical Patents Inc. filed Critical Exxon Chemical Patents Inc.
Priority to EP97953444A priority Critical patent/EP0960087A1/en
Priority to AU57189/98A priority patent/AU5718998A/en
Publication of WO1998029367A1 publication Critical patent/WO1998029367A1/en
Priority to NO993148A priority patent/NO993148L/no

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C11/00Aliphatic unsaturated hydrocarbons
    • C07C11/02Alkenes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00Purification; Separation; Use of additives
    • C07C7/144Purification; Separation; Use of additives using membranes, e.g. selective permeation

Definitions

  • the present invention relates to a simplified system for separating olefins from non-olefins in a product stream. More particularly, the invention relates to the use of a facilitated transport membrane to separate olefins from an olefins-rich product stream.
  • Olefins such as ethylene and propylene
  • Olefins and a myriad of byproducts such as ethane, propane, hydrogen, and carbon monoxide, among others, are produced in a single stream obtained from an olefins generation/preparation process. Before the olefins can be sold, the olefins must be separated from these myriad byproducts.
  • Olefin products generally are required to have greater than about 98 wt% purity, and to contain substantially inert components, such as methane and ethane, in proportions less than about 2000 molar ppm each.
  • Potentially reactive components such as hydrogen, carbon monoxide, carbon dioxide, and others, can be present only in proportions less than about 20 molar ppm each.
  • ethylene has a very low normal boiling point
  • very low temperature vapor-liquid flash and fractional distillation techniques are required to obtain a high recovery of ethylene in a product stream.
  • Many ethylene recovery and separation processes require temperatures as low as -215 °F in certain equipment.
  • Special metallurgies and refrigeration systems known as the chill train, the demethanizer tower, and a substantially dedicated refrigeration system, are required to operate equipment at such low temperatures.
  • the cost of purchasing and running the chill train, the demethanizer tower, and related low temperature equipment accounts for much of the total capital cost and energy consumption of ethylene manufacture.
  • Facilitated transport membranes have been used successfully to separate saturated from unsaturated hydrocarbons in pyrolytically processed hydrocarbon streams. However, the preferential passage of unsaturated hydrocarbons through such membranes is facilitated by metal ions or salts, which are likely to also preferentially bind with components found in a methanol to olefin stream, such as carbon monoxide, which are not found in a pyrolytically cracked stream. It previously has not been established whether facilitated transport membranes can be used to separate olefins-rich product streams, such as methanol to olefin product streams.
  • the present invention provides a method and apparatus for separating olefins from an olefins-rich product stream comprising producing a product stream comprising at least about 60% olefins, passing said product stream through an olefins selective facilitated transfer membrane, and immediately thereafter collecting a permeate stream comprising about 0.2 wt% saturates or less.
  • Fig. 1 is a schematic diagram of a system incorporating facilitated membrane separation of an olefins-rich product stream according to the present invention.
  • the present invention provides a simplified separation scheme using a selective, facilitated transport membrane to reject saturated hydrocarbons from unsaturated hydrocarbons in an olefins-rich product stream.
  • the olefins-rich product stream comprises at least about 60% olefins.
  • Many methods are under development as alternative methods for producing olefins.
  • the present invention should be useful in conjunction with any of such methods.
  • a preferred olefins-rich product stream for use in the present invention is a methanol to olefin product stream.
  • Appatus typically is used in the context of a single device; however, for purposes of the present invention, the term “apparatus” is defined to encompass several systems.
  • an olefins-rich product stream 11 preferably produced by a methanol to olefin system 10, is fed into the apparatus of the present invention.
  • the product stream 11 is first subjected to a water removal system 12.
  • Suitable water removal systems include, but are not necessarily limited to compression followed by expansion or adsorption on alumina or molecular sieve drying agents.
  • An additional consideration is that the membrane performance is enhanced by the presence of some amount of water vapor in the stream to be separated.
  • the product stream A is passed to an olefins selective membrane module 14.
  • the olefins selective membrane module 14 comprises two chambers separated by an olefins selective facilitated transfer membrane 15 such as that described in US-A-5,062,866, incorporated herein by reference.
  • the olefins-rich product stream 11 flows into a retentate chamber 13 in contact with the membrane 15.
  • the membrane 15 preferably is oriented so that the greatest surface area possible is exposed to the product stream.
  • the olefins in the product stream held in the retentate chamber 13 preferentially cross the membrane into the permeate chamber 14 producing an olefins-rich permeate stream comprising about 0.2 wt% saturates or less, preferably about 0.1 wt% saturates or less.
  • the olefins-rich permeate stream 16 is sent through an adsorber 18 or a series of adsorbers to remove residual carbon monoxide, water, and other byproducts.
  • Suitable adsorption agents include, but are not necessarily limited to molecular sieves and alumina. Alternately, the permeate stream 16 may be treated in a reactive separation step to effect the removal of these by-products.
  • cryogenic separator 20 This separation actually may be a single cryogenic separation device such as a C2-C3 splitter or a series of separation steps depending upon the particular make up of stream 16.
  • further separation and purification of the heavy fraction E from this second cryogenic tower 24 may or may not be advisable.
  • a key feature of the invention is that neither a demethanizer nor a deethanizer is required in order to recover the final olefins product from the olefins-rich product stream.
  • the separation of ethane from ethylene and of propane from propylene is thus much easier and much less expensive than when a deethanizer and/or a demethanizer is required.
  • olefins selective facilitated transfer membrane is defined as follows.
  • the olefins selected facilitated transfer membrane is prepared from at least one hydrophilic polymer associated with a complexing metal ion or salt and a hydrophilic salt of a Group I metal.
  • Suitable polymers for preparing the membranes include, but are not necessarily limited to polyvinyl alcohol, polyvinyl acetate, sulfonyl- containing polymers, polyvinylpyrrolidone, polyethylene oxide, and polyacrylamide, as well as blends of two or more of these polymers, and copolymers of these polymers.
  • a preferred polymer is polyvinyl alcohol.
  • the polymers should be capable of undergoing cross- linking in the presence of an effective amount of cross-linking agent under suitable conditions.
  • the polymer matrix also comprises metal ions or salts which can reversibly complex with aliphatically unsaturated hydrocarbons.
  • the metal ion or salt preferably should be non-reactive, or at least not significantly more reactive than other components in a methanol to olefin product stream than with unsaturated hydrocarbons in order to maintain selectivity of the membrane for the unsaturated hydrocarbons, as well as to avoid fouling of the membrane with undesired reaction by-products.
  • Suitable metals which may be used alone or in various combinations, in the presence or absence of non-metal or non-complexing metal ions, comprise the transition metals of the Periodic Table of the Elements having atomic numbers above 20.
  • useful metals are those of the first transition series having atomic numbers from 21 to 29, such as chromium, copper, manganese, and the iron group metals, such as nickel and iron.
  • Other useful complex-forming metals are in the second and third transition series, i.e., having atomic numbers from 39 to 47 or 57 to 79, such as molybdenum, tungsten, and rhenium, as well as mercury.
  • the noble metals such as silver, gold, and platinum group, among which are platinum, palladium, rhodium, ruthenium, and osmium, are also suitable.
  • Preferred metals are the noble metals, particularly silver, which may be present in the polymer as the ion (preferably in the +1 state, Ag ) or as a metal salt, such as AgN03, Ag(NH3)2 + , or Ag(-pyridine)2 + .
  • the amount of complex-forming metal present in the polymer may vary, but should be sufficient to accomplish the desired separation, and preferably sufficient to provide an adequate complexing rate with minimal membrane surface area.
  • the membranes may be made by first forming a polymer solution comprising one or more of the foregoing polymers and at least one of the foregoing metal ions or salts in a solvent, preferably water.
  • the polymer solution further comprises a cross-linking agent in an amount effective to promote cross-linking of the polymer under suitable conditions.
  • Suitable cross-linking agents include, but are not necessarily limited to, formaldehyde, divinyl sulfone, toluene diisocyanate, glyoxal, trimethylol melamine, terephthalaldehyde, epichlorohydrin, vinyl acrylate, and maleic anhydride. Formaldehyde, divinyl sulfone and toluene diisocyanate are preferred.
  • the polymer solution comprises an effective amount of at least one compound selected from hydrophilic salts of metals of Group I of the Periodic Table of the Elements.
  • Suitable salts include, but are not necessarily limited to, sodium nitrate, sodium methyl sulfonate, potassium nitrate, potassium methyl sulfonate, and lithium nitrate.
  • the same anion should be present in both the transition metal complex and in the Group I metal salt.
  • such salts preferably comprise between about 1 to 8 wt%.
  • the presence of salts of Group I metals in the membrane is believed to increase hydrated water content in the membrane, which may enhance diffusion of the transition metal-olefin complex and accompanying complexing and decomplexing with the olefin.
  • Group I metal nitrates are believed to assist in maintaining the transition metal complex in an oxidation state which is effective for complexing with the olefin.
  • the polymer solution should be cast onto a solid support using casting techniques known in the art, for example, "knife-casting" or “dip-casting.”
  • a cross-linking agent is present in the polymer solution, the membrane after casting is treated under temperature conditions sufficient to effect cross- linking of the polymer but insufficient to reduce the hydrocarbon-complexing metal ion or salt.
  • the resulting membranes are "solid, homogenous" membranes in the sense that they comprise a single polymeric phase in the substantial absence of a liquid phase.
  • the membranes may be as thin as 0.1 ⁇ m, but preferably should be at least about 0.5 ⁇ m, and most preferably between about 1 ⁇ m and about 15 ⁇ m.
  • Olefins having from 2 to about 20 carbon atoms per molecule, preferably 2 to 8 carbon atoms, and most preferably 2 to 3 carbon atoms per molecule may be separated from methanol to olefin product streams according to the present invention.
  • the feedstream should be contacted with a first side of the membrane of the invention and a permeate collected at a second side of the membrane comprising the aliphatically unsaturated hydrocarbon in increased concentration relative to the feedstream.
  • permeate is meant that portion of the feedstream that is withdrawn at the second side of the membrane, exclusive of sweep gas and other fluids.
  • the olefins of the feedstream are in the vapor phase, and a driving force for permeation is maintained by a partial pressure differential across the membrane.
  • the partial pressure differential preferably should be in the range of about 0.01 atm (0.15 psi) to 55 atm (809 psi), and more preferably about 0.5 atm (7.4 psi) to 30 atm (441 psi).
  • the partial pressure differential is preferentially established by compression of the feedstream to an elevated pressure and drawing the olefins rich product stream off at a reduced pressure.
  • the differential partial pressure may be aided by the application on the permeate side of vacuum, sweep gas or sweep liquid.
  • a sweep gas or liquid is employed, the gas or liquid is preferably essentially inert with respect to the metal ions in the membrane and is easily removed from the olefin rich permeate stream. It may be preferable to introduce the sweep gas or liquid in a countercurrent fashion.
  • Suitable sweep flluids include but are not necessarily limited to C4 + olefins or paraffins or mixtures thereof. It will be appreciated by persons of skill in the art that the inclusion of a sweep fluid will necessitate the inclusion of an additional separation step or increased duty on an already included separation.
  • the feed is maintained under conditions of temperature and pressure such that substantially all of the olefins in the feedstream are in the liquid phase, and the unsaturated hydrocarbon is recovered under vacuum in the vapor phase (i.e., pervaporated) at the permeate side of the membrane.
  • the vacuum on the permeate side of the membrane can range between about 1 mm Hg to about 750 mm Hg (0.99 atm or 14.5 psi) at room temperature. This embodiment is not preferred because of the low temperatures, and concomitant cost, that would be required to maintain ethylene and/or propylene-preferred products of the present process-in a liquid phase.
  • the membrane may be in the form of hollow fibers, tubes, films, sheets, etc.
  • the process is conveniently carried out in a permeation cell divided into compartments by a membrane, with the compartments having means for removing the contents therefrom.
  • the specific design and configuration of the permeation cell may vary according to individual requirements of capacity, flow rate, etc.
  • the process may be carried out continuously or batchwise, in a single or multiple stages, but preferably in a continuous manner.
  • the relative rate of transport of the alkenes examined was roughly 1000 times faster than for the alkanes. While CO2 and CO were transported somewhat faster than the alkanes, they were still, respectively, 5 or 80 times slower than ethylene or propylene. The net result was that the concentration of methane, ethane, and propane was greatly reduced in the stream passing through the membrane ("permeate").
  • the ratio of (methane+ethane)/ethylene is considered to be a "figure of merit" for the separation.
  • a methanol to olefin product stream is processed by the system schematically diagramed in Fig. 1 and described in detail above.
  • a flow rate of 100 Ib hr ethylene the following are the flow rates of the other products of the system:

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Analytical Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Water Supply & Treatment (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)
PCT/US1997/023876 1996-12-31 1997-12-31 Apparatus and method for separating olefins from an olefins-rich product stream WO1998029367A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP97953444A EP0960087A1 (en) 1996-12-31 1997-12-31 Apparatus and method for separating olefins from an olefins-rich product stream
AU57189/98A AU5718998A (en) 1996-12-31 1997-12-31 Apparatus and method for separating olefins from an olefins-rich product stream
NO993148A NO993148L (no) 1996-12-31 1999-06-24 Apparatur og fremgangsmåte for separering av olefiner fra en olefinrik produktström

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US3394996P 1996-12-31 1996-12-31
US60/033,949 1996-12-31

Publications (1)

Publication Number Publication Date
WO1998029367A1 true WO1998029367A1 (en) 1998-07-09

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PCT/US1997/023876 WO1998029367A1 (en) 1996-12-31 1997-12-31 Apparatus and method for separating olefins from an olefins-rich product stream

Country Status (6)

Country Link
EP (1) EP0960087A1 (no)
AR (1) AR015106A1 (no)
AU (1) AU5718998A (no)
NO (1) NO993148L (no)
WO (1) WO1998029367A1 (no)
ZA (1) ZA9711644B (no)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112592251A (zh) * 2020-12-23 2021-04-02 上海睿碳能源科技有限公司 用于分离含轻烃物流的方法和设备

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2980476B1 (fr) 2011-09-27 2013-08-30 Arkema France Procede de valorisation de produits nobles dans un procede de production de (meth)acrylates de dialkylaminoalkyle

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995006018A1 (en) * 1993-08-27 1995-03-02 Chevron U.S.A. Inc. Dehydrogenation using dehydrogenation catalyst and polymer-porous solid composite membrane

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995006018A1 (en) * 1993-08-27 1995-03-02 Chevron U.S.A. Inc. Dehydrogenation using dehydrogenation catalyst and polymer-porous solid composite membrane

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112592251A (zh) * 2020-12-23 2021-04-02 上海睿碳能源科技有限公司 用于分离含轻烃物流的方法和设备

Also Published As

Publication number Publication date
EP0960087A1 (en) 1999-12-01
AR015106A1 (es) 2001-04-18
NO993148D0 (no) 1999-06-24
ZA9711644B (en) 1998-12-07
NO993148L (no) 1999-06-24
AU5718998A (en) 1998-07-31

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