Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D69/00—Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
  • B01D69/12—Composite membranes; Ultra-thin membranes
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
  • B01D53/22—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by diffusion
  • B01D53/228—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by diffusion characterised by specific membranes
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D63/00—Apparatus in general for separation processes using semi-permeable membranes
  • B01D63/10—Spiral-wound membrane modules
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D69/00—Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
  • B01D69/02—Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor characterised by their properties
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
  • B01D71/06—Organic material
  • B01D71/30—Polyalkenyl halides
  • B01D71/32—Polyalkenyl halides containing fluorine atoms
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
  • B01D71/06—Organic material
  • B01D71/30—Polyalkenyl halides
  • B01D71/32—Polyalkenyl halides containing fluorine atoms
  • B01D71/34—Polyvinylidene fluoride
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
  • B01D71/06—Organic material
  • B01D71/30—Polyalkenyl halides
  • B01D71/32—Polyalkenyl halides containing fluorine atoms
  • B01D71/36—Polytetrafluoroethylene
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
  • B01D71/06—Organic material
  • B01D71/44—Polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, not provided for in a single one of groups B01D71/26-B01D71/42
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
  • B01D71/06—Organic material
  • B01D71/70—Polymers having silicon in the main chain, with or without sulfur, nitrogen, oxygen or carbon only
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
  • B01D71/06—Organic material
  • B01D71/76—Macromolecular material not specifically provided for in a single one of groups B01D71/08 - B01D71/74
  • B01D71/82—Macromolecular material not specifically provided for in a single one of groups B01D71/08 - B01D71/74 characterised by the presence of specified groups, e.g. introduced by chemical after-treatment
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2256/00—Main component in the product gas stream after treatment
  • B01D2256/22—Carbon dioxide
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2256/00—Main component in the product gas stream after treatment
  • B01D2256/24—Hydrocarbons
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2257/00—Components to be removed
  • B01D2257/10—Single element gases other than halogens
  • B01D2257/102—Nitrogen
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2257/00—Components to be removed
  • B01D2257/70—Organic compounds not provided for in groups B01D2257/00 - B01D2257/602
  • B01D2257/702—Hydrocarbons
  • B01D2257/7022—Aliphatic hydrocarbons
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2323/00—Details relating to membrane preparation
  • B01D2323/15—Use of additives
  • B01D2323/218—Additive materials
  • B01D2323/2181—Inorganic additives
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2325/00—Details relating to properties of membranes
  • B01D2325/04—Characteristic thickness
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2325/00—Details relating to properties of membranes
  • B01D2325/14—Membrane materials having negatively charged functional groups
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2325/00—Details relating to properties of membranes
  • B01D2325/20—Specific permeability or cut-off range
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2325/00—Details relating to properties of membranes
  • B01D2325/32—Melting point or glass-transition temperatures
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02C—CAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]
  • Y02C20/00—Capture or disposal of greenhouse gases
  • Y02C20/40—Capture or disposal of greenhouse gases of CO2

Definitions

• Membranes can be used for separation of gas mixtures that are produced in industrial processes, such as energy production. These separations can include separation of alkenes from alkanes such as propylene from propane in hydrocarbon refinery operations, separation of carbon dioxide from hydrocarbons such as methane (/.e., biogas), or separation of carbon dioxide from nitrogen in effluent streams from the combustion of hydrocarbons (/.e., flue gases).
• alkenes from alkanes such as propylene from propane in hydrocarbon refinery operations
• separation of carbon dioxide from hydrocarbons such as methane (/.e., biogas)
• separation of carbon dioxide from nitrogen in effluent streams from the combustion of hydrocarbons /.e., flue gases
• Useful membranes can include composite membranes that have a thin gas- separation layer contacted to a high-diffusion rate layer (gutter layer) for increased permeance, and a porous-layer support for overall strength and durability.
• gutter layer high-diffusion rate layer
• porous-layer support for overall strength and durability.
• weakly adhered layers may be prone to delamination and damage from a fabrication process for making large-area modules for commercial applications.
• a delaminated or damaged gas- separation layer can have reduced performance with lower gas-separation selectivity.
• a thin-film composite membrane having improved adhesion between a gutter layer and a fluorinated ionomer in a gas- separation layer.
• the membrane can have greater permeability compared to a comparable membrane without a gutter layer.
• the thin-film composite membrane comprises a porous-layer support; a gas-separation layer comprising a fluorinated ionomer; and a gutter layer comprising a polymer material having a glass transition temperature greater than 100°C.
• the polymer material is selected from a substituted polyacetylene comprising a repeating unit structure (I), an addition-polymerized and substituted polynorbornene comprising a repeating unit structure (II), or an addition- polymerized and substituted polytricyclononene comprising a repeating unit structure (III) as folllows:
• n is a number that defines the degree of polymerization;
• R 1 comprises an alkyl or an aromatic group;
• R 2 comprises an aromatic group or a silyl group;
• R 3 is H or comprises an alkyl group, a silyl group, or an alkoxy-silyl group;
• R 4 comprises a silyl group, or an alkoxy-silyl group;
• R 5 is H or comprises a silyl group or an alkoxy- silyl group;
• R 6 comprises a silyl group or an alkoxy-silyl group;
• R 7 is H, or if R 5 is H, then R 7 comprises a silyl group or an alkoxy-silyl group.
• the substituted polyacetylene can be poly(1- trimethylsilyl propyne)
• the addition polymerized and substituted polynorbornene can be poly(5-trimethylsilyl norborn-2-ene)
• the addition-polymerized and substituted polytricyclononene can be poly(3,3-bis(trimethylsilyl)tricyclonon-7-ene).
• the polymer material can have an intrinsic permeability to carbon dioxide that is greater than 2800 Barrer (8.04 x 10 13 mol m/(m 2 s Pa)) and the gutter layer thickness can be between 0.1 pm and 1pm.
• the porous-layer support for the gutter layer can comprise polyvinylidine fluoride, expanded polytetrafluoroethylene, polyacrylonitrile, polysulfone, or polyethersulfone.
• the fluorinated ionomer can comprise polymerized repeating units of tetrafluoroethylene and a perfluorovinyl ether monomer comprising a pendant sulfonic acid or sulfonate functionality.
• the sulfonate functionality can be selected from silver sulfonate, ammonium sulfonate, alkyl ammonium sulfonate, lithium sulfonate, or sodium sulfonate.
• the gas separation layer thickness can be between 0.02pm and 0.5pm.
• a spiral-would membrane module comprising the thin-film composite membrane as described herein.
• a process for separating an alkene from a first gas mixture comprising providing a thin-film composite membrane as described herein having silver sulfonate functionality, a feed side, and a permeate side; exposing the feed side to the first gas mixture that is flowing; providing a driving force across the thin-film composite membrane; and producing a second gas mixture on the permeate side that has a higher concentration of alkene than the concentration of alkene in the first gas mixture.
• the first gas mixture comprises propylene and propane and further comprises water vapor.
• a process for separating carbon dioxide from a first gas mixture comprising: providing a thin-film composite membrane as described herein, having a feed side and a permeate side; exposing the feed side to the first gas mixture that is flowing; providing a driving force across the thin-film composite membrane; and producing a second gas mixture on the permeate side that has a higher concentration of carbon dioxide than the concentration of carbon dioxide in the first gas mixture.
• the first gas mixture further comprises nitrogen, methane, or water vapor.
• Providing a driving force can comprise applying a vacuum to the permeate side.
• the terms “comprises,” “comprising,” “includes,” “including,” “has,” “having” or any other variation thereof, are intended to cover a non-exclusive inclusion.
• a process, method, article, or apparatus that comprises a list of elements is not necessarily limited to only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus.
• use of "a” or “an” are employed to describe elements and components described herein. This is done merely for convenience and for a general sense of the scope of the invention. This description should be read to include one or at least one; the singular also includes the plural unless it is obvious that it is meant otherwise. Certain additional terms are also used and some of them are further defined within the following detailed description of the invention.
• a gas-separation layer for a composite membrane can be fabricated from a fluorinated ionomer comprising sulfonate or sulfonic acid functionality such as disclosed in U.S. Patent Serial No. 5,191,151 and U.S. Patent Serial No. 10,639,591.
• a high-diffusion rate layer which is also known as a gutter layer in the field of membrane technology, can provide overall greater permeability and can be situated (layered) between the gas-separation layer and a porous-layer support, for overall greater strength and durability.
• a composite membrane having a gas-separation layer from a fluorinated ionomer and a gutter layer are described in U.S. Patent Serial No.
• the gutter layer was prepared by solution casting a fluorinated polymer material, such as Teflon® AF 2400, which was pre-dissolved in a fluorinated solvent, onto the porous- layer support.
• the gas-separation layer was subsequently fabricated by coating (i.e. , solution casting) the fluorinated ionomerfrom a non-fluorinated solvent on top of the gutter layer.
• Fluorinated ionomers are hydrophilic and can absorb and permeate liquid water whereas a gutter layer, such as from Teflon® AF 2400, is also fluorinated, hydrophobic, and repels liquid water but can permeate water vapor. While both materials may be fluorinated, this like vs like nature may be insufficient for good layer adhesion and operational lifetime in a humidified environment.
• a weakly adhered gas-separation layer from a fluorinated ionomer having silver sulfonate functionality can separate from the gutter layer, such as by pulling apart with adhesive tape, and may be prone to delamination and damage from a fabrication process into large-area modules for commercial applications.
• a delaminated or damaged gas-separation layer can have reduced performance with lower gas-separation selectivity.
• a thin-film composite membrane having improved adhesion between a gutter layer and the fluorinated ionomer in a gas-separation layer with overall greater permeability for the composite membrane versus a comparable composite membrane without a gutter layer is desirable.
• a thin-film composite membrane that has surprisingly improved adhesion between a fluorinated ionomer in a gas-separation layer and a gutter layer comprising a polymer material, which is chemically dissimilar, non-fluorinated, and hydrophobic.
• the gas-separation layer is laminated to the gutter layer, which is laminated to a porous-layer support.
• the gas-separation layer and the gutter layer are not separated (i.e., peeled apart) using painter’s masking tape, unlike a composite membrane having a gutter layer made from Teflon® AF 2400.
• the polymer material for incorporation in the gutter layer is selected from a substituted polyacetylene, an addition-polymerized and substituted polynorbornene, or an addition-polymerized and substituted polytricyclononene.
• the substituted polyacetylene can include poly(1 -trimethylsilyl propyne) (PTMSP), the addition-polymerized and substituted polynorbornene can include poly(5-trimethylsilyl norborn-2-ene) (PTMSN), or the addition-polymerized and substituted polytricyclononene can include poly(3,3-bis(trimethylsilyl)-tricyclonon-7- ene) (PTCNSi2g). Structures for these specific polymer materials are shown in (1 ), (2), and (3), respectively.
• the improved adhesion between the gas-separation layer and the gutter layer enables fabrication of the thin-film composite membrane into large-area modules with fewer defects.
• the thin-film composite membrane is useful for separation of alkenes from alkanes or separation of alkenes from other gases such as nitrogen.
• the thin-film composite membrane may be used for separation of carbon dioxide from gases such as nitrogen, an alkane, or an alkene.
• PTMSP poly(trimethylsilyl propyne)
• Substituted polyacetylenes, addition-polymerized and substituted polynorbornenes, or addition-polymerized and substituted polytricyclononenes can have high intrinsic gas permeability but low to moderate gas-separation selectivity.
• a gutter layer incorporating the polymer material in combination with a gas- separation layer incorporating the fluorinated ionomer can have equivalent carbon dioxide over nitrogen gas-separation selectivity for the thin-film composite membrane with respect to a composite membrane having the gas-separation layer incorporating the fluorinated ionomer directly on the porous-layer support.
• the thin-film composite membrane can have increased gas-separation selectivity of at least 50%. Equivalent or increased gas-separation selectivity is unexpected since it may be generally understood in the field of membrane technology that gas-separation selectivity was not additive and a gutter layer could increase overall permeance but with a likely cost of reduced gas-separation selectivity.
• Teflon® AF 2400 each of PTMSP, PTMSN, and PTCNSi2g are soluble in organic solvents such as toluene. This solubility avoids use of fluorinated solvents, which can simplify manufacturing, avoid much stricter requirements for solvent recovery, and eliminate any potential for release of fluorinated solvent vapor, which can be a potent greenhouse gas.
• the polymer materials are substituted in that they incorporate functionality in their repeating unit structure.
• PTMSP, PTMSN, or PTCNSi2g are silyl- substituted polymer materials that contain trimethylsilyl groups within their repeating unit structure. The silyl-substitution may help with adhesion to the fluorinated ionomer in the gas-separation layer.
• PTMSP, PTMSN, and PTCNSi2g are also glassy polymer materials having a glass transition temperature greater than 300 Celsius.
• a glass transition temperature that is greater than an anticipated 100 Celsius maximum operating temperature for the thin-film composite membrane may help to stabilize the interface between the gas-separation layer and the gutter layer and help to retain or possibly enhance gas-separation selectivity with respect to a comparable membrane with a gas-separation layer directly on the porous-layer support.
• a substituted polynorbornene or substituted polytricyclononene is addition polymerized. Unlike other possible polymerization techniques such as ring opening metathesis or radical polymerization, the fused ring structure with monomer polymerization to said addition-polymerized polymer materials remains intact and unrearranged. The fused ring structure is therefore bulkier from addition polymerization, resulting in high gas permeability.
• the reported intrinsic permeabilities of PTMSN and PTCNSi2g, for carbon dioxide are approximately 5,300 and 19,900 Barrer, respectively.
• PTMSP has an initial carbon dioxide permeability of 34,000 Barrer and its synthesis may also be viewed as an addition polymerization.
• PTMSP does not contain a fused ring structure and its high permeability is due instead to a high free volume from inefficient chain packing of a rigid (vs. bulky) backbone structure.
• PTMSN, PTCNSi2g, and PTMSP are preferred polymer materials having a permeability greater than the reported 2800 Barrer (8.04 x 10 13 mol m/(m 2 s Pa)) for Teflon® AF 2400.
• substituted polyacetylenes may have glass transition temperatures of at least 100 Celsius, may have an intrinsic permeability to carbon dioxide that is greater than 2800 Barrer, and may be suitable for incorporation in the gutter layer.
• General structures for a polymer material having silyl substitution, alkoxy-silyl substitution, or aromatic substitution, in addition to alkyl groups, are shown below.
• the substituted polyacetylene comprises a repeating unit structure (I)
• the addition-polymerized and substituted polynorbornene comprises a repeating unit structure (II)
• the addition-polymerized and substituted polytricyclononene comprises a repeating unit structure (III).
• the polymer material may be a homopolymer or a copolymer where n is a number that defines the degree of polymerization;
• R 1 comprises an alkyl or an aromatic group;
• R 2 comprises an aromatic group or a silyl group;
• R 3 is H or comprises an alkyl group, a silyl group, or an alkoxy-silyl group;
• R 4 comprises a silyl group, or an alkoxy-silyl group;
• R 5 is H or comprises a silyl group or an alkoxy-silyl group;
• R 6 comprises a silyl group or an alkoxy-silyl group;
• R 7 is H, or if R 5 is H, then R 7 comprises a silyl group or an alkoxy-silyl group. substituted polyacetylene
• substituted polyacetylenes may include certain indan-containing poly(diphenylacetylene) derivatives that were disclosed by Hu et al. in “Synthesis and Properties of Indan-Based Polyacetylenes That Feature the Highest Gas Permeability among All the Existing Polymers” Macromolecules 2008, 41, 8525- 8532.
• Other addition-polymerized substituted polynorbornenes may include alkoxysilyl-substituted polynorbornenes such as disclosed by Maroon et al. in “Addition-type alkoxysilyl-substituted polynorbornenes for post-combustion carbon dioxide separations” Journal of Membrane Science, 595, February 2020, 117532.
• PTMSP is commercially available from Gelest (Morrisville, PA) and is soluble in organic solvents that include toluene, cyclohexane, heptane, and chloroform.
• PTMSN may be synthesized by addition polymerization of 5-trimethylsilyl-2- norbornene as disclosed by Finkelshtein et al. in “Addition-Type Polynorbornenes with Si(CH3)3 Side Groups: Synthesis, Gas Permeability, and Free Volume” Macromolecules 2006, 39, 7022-7029.
• PTMSN is soluble in organic solvents that include toluene and chloroform.
• PTCNSi2g may be synthesize by addition polymerization of 3,3-bis(trimethylsilyl)tricyclonon-7-ene as disclosed by Gringolts et al. in Russian Patent 2,410,397 or by Chapala et al. in “A Novel, Highly Gas- Permeable Polymer Representing a New Class of Silicon-Containing Polynorbornenes as Efficient Membrane Materials” Macromolecules 2015, 48, 8055- 8061.
• PTCNSi2g is soluble in organic solvents that include toluene and chloroform.
• a supported film that will subsequently become the gutter layer may be prepared by coating (i.e.
• the porous-layer support may be in the form of a flat sheet, hollow fiber, or other tube-like and porous structure.
• the dilute solution of the polymer material may be cast on the outer surface (shell) or the inner surface (lumen).
• a dilute solution of PTMSP, PTMSN, or PTCNSi2g can be prepared in an organic solvent at concentrations that are less than 2%, or between 0.1 % and 1 %.
• Acceptable coating methods include but are not limited to ring casting, dip-coating, spin-coating, slot-die coating, roll coating, Mayer rod coating, and injection coating.
• the organic solvent can be evaporated to form the supported film of the polymer material that will subsequently become the gutter layer. Residual or trace organic solvent remaining in the supported film should not interfere with subsequent fabrication steps.
• the supported film that will subsequently become the gutter layer is thin and can be between 0.05pm to 5-pm, or between 0.1pm to 1pm.
• Permeance which is pressure normalized flux, is typically reported as a gas permeance unit (GPU) coefficient that has units of GPUx10 6 xcm 3 (STP)/(cm 2 s cmHg).
• Permeability is permeance normalized for thickness and is typically reported in Barrer, in which the Barrer permeability coefficient has units of pBarrerXl0 10 xcm 3 (STP)/(cm s cmHg).
• the supported film and porous-layer support can have a helium or carbon dioxide permeance of at least 5000 GPU, or greater than 10,000 GPU, when measured at 25°C.
• the gas-separation layer in the thin-film composite membrane comprises a fluorinated ionomer.
• a fluorinated ionomer is a fluorinated copolymer that has a fluorinated backbone and covalently bound pendant groups that comprise ionic functionality such as sulfonic acid, sulfonate, carboxylic acid, carboxylate, phosphate, or phosphonium. Fluorinated ionomers comprising sulfonic acid or sulfonate functionality may be more preferred. Certain counter ions (cations) to the sulfonate functionality can impart high water permeation to the fluorinated ionomer.
• Suitable cations include alkyl ammonium, ammonium, silver, lithium, ora sodium cation. Sulfonate functionality wherein the cation is silver can be used for a practical separation of alkenes from alkanes.
• the equivalent weight of the fluorinated ionomer is the weight of fluorinated ionomer containing one mole of sulfonate or sulfonic acid functionality.
• the equivalent weight (EW) can be less than 5000 grams per mole, less than 2000, or between 500 and 800-g/mole.
• Suitable fluorinated ionomers can include those comprising polymerized repeating units from tetrafluoroethylene and a perfluorovinyl ether monomer, having a pendant sulfonate or sulfonic acid functionality, such as for example Nafion® (Chemours, Wilmington DE), and Aquivion® (Solvay, Houston TX). Aquivion® has a lower equivalent weight than Nafion®.
• the gas-separation layer may be fabricated by coating (i.e. , solution casting) a dilute solution of the fluorinated ionomer.
• the dilute solution can be prepared at concentrations that are less than 5% (w/w), less than 2%, or between 0.1% and 2%.
• the dilute solution can be prepared by mixing a pre-formed, concentrated, and commercially available solution of the fluorinated ionomer with a solvent that is miscible and non-fluorinated.
• the solvent may be the same or different from the solvent in the pre-formed solution thus forming a solvent mixture.
• Acceptable dilute solution coating methods include ring casting, dip-coating, spin-coating, slot-die coating, roll coating, and Mayer rod coating.
• the dilute solution can be coated onto the surface of the film that will become the gutter layer, which can be already on the porous-layer support.
• the solvent or solvent mixture can be removed such as by evaporation.
• the solvent or solvent mixture can evaporate to form the to form the “dry” gas-separation layer in a timely manner.
• the gas-separation layer thickness has a significant influence on permeance of the thin-film composite membrane and is therefore thin with a thickness of 0.01 pm to 5pm, or between 0.02pm to 0.5pm.
• the porous-layer support can reinforce the gutter layer and the gas- separation layer that are thin and helps to strengthen the composite such that the thin-film composite membrane may be fabricated into complex geometries that include spiral-wound or hollow-fiber membrane modules.
• the porous-layer support may be in the form of a flat sheet, hollow fiber, or other tube-like and porous structure. Suitable materials for a porous-layer support include but are not limited to polyvinylidine fluoride, expanded polytetrafluoroethylene, polyacrylonitrile, polysulfone, and polyethersulfone.
• the porous-layer support may also comprise a porous and even stronger backing material such as a non-woven polyester or polypropylene sheet.
• Inorganic substrates such as porous silica or alumina sheets or tubes may also be suitable materials for a porous-layer support.
• the porous-layer support can have a helium or carbon dioxide permeance that is higher than the gutter layer, such as at least 2 times higher, or at least 5 times higher. Permeate gases can flow relatively unobstructed through the porous-layer support having a porosity that is at least 40%.
• the average pore size can be less 0.1 -pm or between 0.01 and 0.03-pm, corresponding to molecular weight cut-offs of approximately 50,000 to 200,000 Daltons, respectively.
• the thin-film composite membrane may be subjected to a thermal treatment step and “annealed” to improve mechanical durability and longer-term performance stability.
• the fluorinated ionomer in the gas-separation layer can be annealed by heating the thin-film composite membrane to near or above the glass transition temperature of the fluorinated ionomer.
• the exact glass transition temperature will be dependent on the composition of the fluorinated ionomer.
• the annealing temperature for the fluorinated ionomer is between 50 and 200°C, and between 75 and 150°C in some instances.
• the thin-film composite membrane can be heated for 0.1 to 10 minutes, or for 1 to 5 minutes. An appropriate annealing temperature and time should not degrade the other components of the improved thin-film composite membrane.
• the fluorinated ionomer comprising sulfonic acid or sulfonate functionality other than silver sulfonate functionality in the gas-separation layer is initially inactive for separation of alkenes from alkanes. That is, the thin-film composite membrane is not significantly perm-selective (selectivity ⁇ 5) and the alkene permeance is low ( ⁇ 25-GPU).
• the thin-film composite membrane may be activated by exchange of protons or other cations (counter ions) for silver in the gas-separation layer.
• the exchange may be carried out by contacting the exposed surface of the gas-separation layer with a solution comprising water and a soluble and ionizable silver compound such as silver nitrate.
• a sufficient level of exchange can quickly occur for a thin (£2miti) gas-separation layer as evidenced by a high permeance (>100-GPU) and selectivity (>25) for propylene over propane after less than 1 minute of contact with aqueous silver nitrate at ambient ( ⁇ 23°C) temperature.
• the thin-film composite membrane has improved adhesion between the fluorinated ionomer in the gas-separation layer and the polymer material in the gutter layer with respect to a comparative composite membrane having a gutter layer from, Teflon® AF 2400.
• the improved adhesion is evident from a peel test using painter’s masking tape to separate the gas-separation layer from the underlying gutter layer and wherein the fluorinated ionomer comprises sulfonate functionality such as silver sulfonate, lithium sulfonate, or sodium sulfonate.
• the painter’s masking tape such as manufactured by 3M (St.
• the thin-film composite membrane wherein the counter ion to the fluorinated ionomer is silver, can be useful for the separation of an alkene from an alkane, such as propylene from propane, or separation of an alkene from nitrogen.
• an alkane such as propylene from propane
• the thin-film composite membrane may be useful for the separation of carbon dioxide from nitrogen or separation of carbon dioxide from an alkane such as methane.
• the thin-film composite membrane may be useful for separation of carbon dioxide from an alkene such as ethene.
• the thin-film composite membrane is exposed to a flowing gaseous feed-mixture comprising an alkene or carbon dioxide.
• a “driving force” is provided across the thin-film composite membrane in which the partial pressure of the alkene or carbon dioxide on the feed- side is higher than on the permeate-side of the thin-film composite membrane.
• the driving force may include applying a vacuum on the permeate-side and may be preferred, due to lower energy consumption, for separation of carbon dioxide from nitrogen in flue gas in electrical generation plants powered by fossil fuels.
• Gas separation of the alkene or carbon dioxide from the gaseous feed-mixture occurs through the membrane producing a permeate mixture at the membrane permeate- side having a higher concentration of alkene or carbon dioxide than the feed-mixture.
• the performance of the thin-film composite membrane may be enhanced by having water vapor in the feed mixture and optionally in a sweep gas comprising water vapor at the permeate-side, which may also function to increase the driving force by reducing the alkene or carbon dioxide concentration.
• Spiral-wound modules are highly useful for large-scale membrane separations and are an efficient means to assemble large-area flat sheets of the thin- film composite membrane into a compact volume.
• Spiral-wound module design and construction are well documented in the literature.
• a flat- sheet membrane is folded into a rectangular and slightly asymmetric membrane leaf with the feed side facing outward.
• the membrane is glued along three sides into a pocket shape with a plastic mesh spacer inside for permeate gas flow.
• the partly exposed spacer in the asymmetric pocket is sealed (glued) along its edges to a perforated core tube, and then the leaf or multiple leaves, with additional interleafed mesh spacers for feed flow, are wound around the core tube.
• the outside of the wound module is wrapped with adhesive tape to hold the module components in place.
• a spiral-wound module may be configured within a pressure vessel for gas separation.
• a pressurized feed-gas flow is passed through the open mesh channels of the feed spacers parallel to the long axis of the spiral-wound module and certain components permeate the thin-film composite membrane.
• the permeated components flow through the open mesh channels of the permeate spacers within a spiral leaf, perpendicular to the long axis and feed flow.
• the permeated components exit the permeate spacers and are collected in the core tube.
• Other spiral-wound module designs may be constructed in a similar manner that will allow for a sweep gas or fluid to circulate through the permeate side of the membrane leaf in addition to the core tube. This may be achieved by adding flow-directing elements to the core tube and within the permeate spacers of the pocket-shaped leaf.
• PTMSP Poly(trimethylsilyl propyne)
• PTMSP Poly(trimethylsilyl propyne)
• Teflon® AF 2400 was dissolved to 0.5% (w/w) in Opteon® SF10 and filtered through 1pm glass microfiber.
• the solutions were then separately cast, using a vertical roll coater, on a 100cm x 200cm porous-layer support comprising polyvinylidine fluoride (PVDF) ultra-filtration membrane, having a molecular weight cut-off of 100,000 Daltons, on a non-woven polyester backing (Synder, Filtration, Vacaville CA).
• PVDF polyvinylidine fluoride
• the solvents were evaporated at ambient room temperature under a dry nitrogen atmosphere to form the supported films that will become the gutter layers.
• An apparent laminar thickness for the PTMSP supported film was gravimetrically estimated at O.dOmiti using the applied solution mass, concentration, porous-layer support area, and a PTMSP density of 0.77-g/mL.
• An apparent laminar thickness for the Teflon® AF 2400 supported film control was similarly estimated at 0.25pm using a Teflon® AF 2400 density of 1.67- g/mL.
• a 47-mm diameter sample from each supported film was separately placed in a stainless-steel crossflow cell.
• the supported film was tested for helium permeance at ambient room temperature ( ⁇ 24°C) at 5 to 10 psig feed pressure at 200-mL/min (STP) and a gauge permeate pressure.
• Permeate gas flowrate was measured using an Agilent ADM flow meter, modelG6691A.
• the PTMSP supported film had a helium permeance of approximately 5800GPU at pressures between 5 and 10psig.
• the Teflon® AF 2400 supported film had a helium permeance of approximately 7900 GPU.
• the isopropanol and water were evaporated at ambient room temperature under a nitrogen atmosphere to form the gas-separation layer.
• the gas-separation layer for each thin-film composite membrane was subsequently annealed at 120 to 130°C for approximately 1 minute by infrared heating.
• An apparent laminar thickness for the gas-separation layer on the PTMSP gutter layer was gravi metrically estimated at 0.62miti using the applied solution mass, concentration, membrane area, and Solvay’s reported Aquivion® density of 2.07-g/mL.
• An apparent laminar thickness for the gas-separation layer on the Teflon® AF 2400 gutter layer control was similarly estimated at 0.69miti.
• the permeate flowrate was measured using an Agilent ADM flow meter, modelG6691 A.
• Helium (He) permeances were less than 25 GPU and an estimate for the thickness of the thin-film composite membranes from helium permeance was calculated by dividing a helium permeability of 22 Barrers for Aquivion® (20 Barrers for Nafion®) in the gas-separation layer by the measured helium permeance using the dry permeability disclosed by Baschetti et al. in “Gas permeation in perfluorosulfonated membranes: Influence of temperature and relative humidity” International Journal of Hydrogen Energy 38 (2013) 11973-11982.
• the samples were subsequently tested for beginning of life performance for separation of a 50/50 feed mixture of propylene and propane.
• the 50/50 feed mixture at 200-mL/min (STP) was first passed through a water bubbler for humidification at ambient room temperature before entering the crossflow cell, also at ambient room temperature.
• a backflow pressure regulator at the retentate outlet maintained the feed pressure at 60-psig.
• the stage cut was less than 5% and the permeate flowrate (at atmospheric pressure) was measured using a soap-film flowmeter.
• the permeate composition was measured by gas chromatography.
• Table 1 summarizes the thickness of the thin-film composite membrane calculated from helium permeance and the beginning of life separation performance. At least three samples of each thin-film composite membrane were tested, and average (Avg) values and standard deviations (SDev) are shown. Membranes having a PTMSP or Teflon® AF 2400 gutter layer had at least 50% higher average propylene (C3H6) over propane (C3H8) separation selectivity in addition to the expected increased permeance that was at least 75% higher.
• Example 5 [0039] PTMSN or PTCNSi2g gutter layer fabrication on a porous-layer support: A 5% (w/w) solution of poly(5-trimethylsilyl norbornene) (PTMSN) in toluene is diluted with heptane to 0.5% and filtered through 1 pm glass microfiber. A 0.5% (w/w) solution of PTCNSi2g is prepared in heptane and filtered through 1 pm glass microfiber.
• PTMSN poly(5-trimethylsilyl norbornene)
• the solutions are then separately cast, using a vertical roll coater, on a 100cm x 200cm porous-layer support comprising polyvinylidine fluoride (PVDF) ultra filtration membrane, having a molecular weight cut-off of 100,000 Daltons, on a non- woven polyester backing (Synder, Filtration, Vacaville CA).
• PVDF polyvinylidine fluoride
• the solvents are evaporated at ambient room temperature under a dry nitrogen atmosphere to form the gutter layers.
• An apparent laminar thickness for the PTMSN and PTCNSi2g gutter layers is gravimetrically estimated at between 0.75-pm and 0.85-pm using the applied solution mass, concentration, porous-layer support area, and PTMSN or PTCNSi2g densities of 0.88-g/mL and 0.85-g/mL, respectively.
• a 47-mm diameter circle is punched from each of the supported films and separately configured in a stainless-steel crossflow cell.
• the supported films are tested for helium permeance at ambient room temperature ( ⁇ 24°C) at 5psig feed pressure at 200-mL/min (STP), and a gauge permeate pressure. Permeate gas flowrate is measured using an Agilent ADM flow meter, modelG6691 A.
• the helium permeance of the PTMSN supported film is at least 7500 GPU and the PTCNSi2g supported film is at least 8300 GPU.
• the isopropanol and water are evaporated at ambient room temperature under a nitrogen atmosphere to form the gas-separation layer.
• the gas-separation layers on the thin-film composite membranes are subsequently annealed at 120 to 130°C for approximately 1 minute by infrared heating.
• An apparent laminar thickness for the gas-separation layers is gravimetrically estimated at approximately 0.6pm using the applied solution mass, concentration, PTMSN or PTCNSi2g supported film areas, and Solvay’s reported Aquivion® density of 2.07- g/mL.
• Circular 47mm diameter samples from each of the thin-film composite membranes having a PTMSN or PTCNSi2g gutter layer were separately activated by immersion in 0.15 M aqueous silver nitrate for 1 minute. Excess silver nitrate solution was gently blown off with dry air.
• the spiral wound-module having a gutter layer from Teflon® AF 2400 had a nitrogen permeance of approximately 2-GPU.
• the pressure vessels containing the spiral-wound modules were separately configured in an apparatus designed for testing large-area modules for alkene/alkane permeance and separation selectivity at closer to commercial operation conditions.
• the spiral-wound modules were tested with a humidified 60/40 mixture of propylene and propane at a 145-psig feed pressure. The stage cut was 35% and the permeate pressure was 2-psig.
• the spiral wound-module having a gutter layer from Teflon® AF 2400 had a propylene permeance of 50GPU and selectivity over propane of 5.
• the spiral wound-module having a PTMSP gutter layer had a propylene permeance of 105GPU and selectivity over propane of 12.
• the remaining wet film was quickly weighed then dried in a horizontal position at ambient room temperature under a dry nitrogen atmosphere to form the gas-separation layer.
• the thin-film composite membrane was subsequently heat treated in a forced air oven at 120°C for approximately 3 minutes while still in the ring holder.
• a laminar thickness for the gas-separation layer was gravimetrically estimated at O.ddmiti using the applied solution mass, concentration, PTMSP supported-film area, and Chemours’ reported Nafion® density of 1 97-g/mL.
• the thin-film composite membrane was activated with 0.15M silver nitrate then configured in a stainless-steel crossflow cell for beginning of life performance for separation of propylene from propane as described in example 4.
• the membrane thickness from helium permeance was O.qmiti
• the propylene permeance was 90GPU
• the selectivity over propane was 49.
• a second thin-film composite membrane was prepared in the same manner and tested for tape adhesion as outlined in example 7. The gas-separation layer could not be removed with the blue painter’s tape and remained attached to the gutter layer.
• stage cuts were less than 2% and the permeate flow rate at atmospheric pressure was measured using an Agilent 1100 flowmeter.
• the CO2 concentration in the permeate flow was measured using a Landtec 5000 biogas analyzer.
• the calculated CO2 permeance for the thin-film composite membrane having a PTMSP gutter layer was 500 GPU and the selectivity over nitrogen was 40.
• the calculated CO2 permeance for the thin-film composite membrane having no gutter layer was 220 GPU and the selectivity over nitrogen was 35.
• the solution of the fluorinated ionomer was then cast, using a vertical roll coater, onto a PTMSP supported film that was prepared as described in example 1.
• the isopropanol and water were evaporated at ambient room temperature under a nitrogen atmosphere to form the gas-separation layer.
• An apparent laminar thickness for the gas-separation layer on the PTMSP gutter layer was gravimetrically estimated at 1.2miti using an applied solution mass, concentration, PTMSP gutter layer/porous-layer support area, and Solvay’s reported Aquivion® density of 2.07-g/mL.
• the gas-separation layer could not be removed from the gutter layer using blue painter’s tape as described in example 7.
• a circular membrane sample (47mm dia.) was tested as described in example 4 at 50°C for beginning of life separation of propylene from propane. The propylene permeance was 110-GPU and the selectivity over propane was 41.

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