Classifications

• • 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
• • 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
  • 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
  • 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
  • B01D69/1216—Three or more layers
• • 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
  • B01D71/76—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
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
  • B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
  • B32B27/20—Layered products comprising a layer of synthetic resin characterised by the use of special additives using fillers, pigments, thixotroping agents
  • B32B27/205—Layered products comprising a layer of synthetic resin characterised by the use of special additives using fillers, pigments, thixotroping agents the fillers creating voids or cavities, e.g. by stretching
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/28—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/28—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42
  • B32B27/286—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42 comprising polysulphones; polysulfides
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
  • B32B27/322—Layered products comprising a layer of synthetic resin comprising polyolefins comprising halogenated polyolefins, e.g. PTFE
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B3/00—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form
  • B32B3/26—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B3/00—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form
  • B32B3/26—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer
  • B32B3/266—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer characterised by an apertured layer, the apertures going through the whole thickness of the layer, e.g. expanded metal, perforated layer, slit layer regular cells B32B3/12
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C7/00—Purification; Separation; Use of additives
  • C07C7/144—Purification; Separation; Use of additives using membranes, e.g. selective permeation
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F214/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
  • C08F214/18—Monomers containing fluorine
  • C08F214/20—Vinyl fluoride
  • C08F214/202—Vinyl fluoride with fluorinated vinyl ethers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F214/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
  • C08F214/18—Monomers containing fluorine
  • C08F214/26—Tetrafluoroethene
  • C08F214/262—Tetrafluoroethene with fluorinated vinyl ethers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F216/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
  • C08F216/12—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an ether radical
  • C08F216/14—Monomers containing only one unsaturated aliphatic radical
  • C08F216/1408—Monomers containing halogen
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F216/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
  • C08F216/12—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an ether radical
  • C08F216/14—Monomers containing only one unsaturated aliphatic radical
  • C08F216/1466—Monomers containing sulfur
  • C08F216/1475—Monomers containing sulfur and oxygen
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F4/00—Polymerisation catalysts
  • C08F4/28—Oxygen or compounds releasing free oxygen
  • C08F4/32—Organic compounds
  • C08F4/34—Per-compounds with one peroxy-radical
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
  • C08G61/02—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
  • C08G61/10—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aromatic carbon atoms, e.g. polyphenylenes
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D129/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal, or ketal radical; Coating compositions based on hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Coating compositions based on derivatives of such polymers
  • C09D129/10—Homopolymers or copolymers of unsaturated ethers
• • 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
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B2307/00—Properties of the layers or laminate
  • B32B2307/70—Other properties
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B2307/00—Properties of the layers or laminate
  • B32B2307/70—Other properties
  • B32B2307/724—Permeability to gases, adsorption
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B2307/00—Properties of the layers or laminate
  • B32B2307/70—Other properties
  • B32B2307/732—Dimensional properties

Definitions

• Thin film composite membranes which have one or more layers of a certain type of silver ionomer, and which can separate alkanes from a!kenes, are described.
• the separation of these types of compounds, especially those having the same number of carbon atoms, such as ethylene from ethane, propylene from propane, and pentene from pentane are often difficult by other methods, because for instance the boiling points of the alkane and alkene are similar, resulting in high energy requirements. This is especially true for lower boiling materials containing 2 to four carbon atoms, which would require cryogenic distillation, usually very energy intensive.
• TFCs Thin-film composite membranes
• layered construction permits use of material combinations that optimize the performance and durability of the membrane.
• alkane-aikene separation processes using silver ionomers described herein are new TFCs for such separations.
• a membrane having a single layer a "separation layer” (SL), of silver ionomer would be useful.
• SL separation layer
• the silver ionomer is expensive, and in thicker membranes which are required for the membrane to have sufficient strength, the permeance to the aikene, the amount of alkene which can pass through the membrane per unit time is relatively low. Therefore one (or more ) thin separation layers are required for practical membranes.
• a composite membrane with another layer of material which physically supports the entire TFC, and which is laminarly contacting the separation layer can be added. This other layer is nonporous and the material passing through the TFC (in this case one or more aikenes), should also preferably diffuse through this other layer rapidly.
• this other layer is called the high diffusion rate layer (HDR).
• This invention concerns, a thin film composite membrane for the separation of alkanes from aikenes, comprising:
• a fluorinated polymer or ionomer is of the total of the carbon- hydrogen groups and the carbon fluorine groups in the ionomer, about 20% or more are carbon-fluorine groups, preferably about 50% or more, very preferably about 70% or more, especially preferably about 90% or more, and very especially preferably about 95% or more are carbon fluorine groups, or most preferably are perfiuoropolymers.
• a carbon-hydrogen group is meant a hydrogen atom bound directly to a carbon atom, while a carbon-fluorine group is a fluorine atom bound directly to a carbon atom.
• -CF 2 - groups contains 2 carbon fluorine groups
• a -CH 3 group contains 3 carbon-hydrogen groups.
• the carbon-hydrogen groups and the carbon fluorine groups are each 50% of the total of carbon-hydrogen plus carbon-fluorine groups present.
• the carbon-hydrogen groups are 33.3% of the total of the carbon-fluorine plus carbon hydrogen groups present, and the carbon-fluorine groups are 66.7% of the carbon-fluorine and carbon-hydrogen groups present.
• the relative amount of carbon- fluorine and carbon hydrogen groups present can be determined by elemental analysis, N R spectroscopy, for instance using 14 C N R, or a combination of any of these.
• a “driving force" in the separation of the alkene and alkane in the gaseous state is generally meant that the partial pressure of alkene on the first ("feed") side of the membrane is higher than the partial pressure of alkene on the second ("product") side of the membrane. For instance this may be accomplished by several methods or a combination thereof. One is pressurizing first side to increase the partial pressure of alkene on the first side, second is sweeping the second side by inert gas such as nitrogen to lower the partial pressure of the alkene on the second side, and third is reducing pressure of second side by vacuum pump to lower the partial pressure of the alkene on the second side. These and other known methods in the art of applying a driving force may be used.
• Q a is the flow rate of component "a" through the membrane
• F a is the permeance of component a through the membrane
• P1 a is the partial pressure on the first (feed) side
• P2 a is the partial pressure on the second (product) side.
• laminated is meant the two layers concerned are in intimate contact with each other. This is often referred to as “bonded together” although usually no separate adhesive is employed.
• the SL is about 0.1 m to about 1.0 ⁇ thick, more preferably about 0.2 ⁇ to about 0.5 ⁇ thick.
• the relative thinness of this layer help to improve the productivity of the overall separation process per unit area of membrane.
• Polymers useful for the SL are silver ionomers of sulfonic acid containing polymers. Such ionomers are well known in the art, and in some instances known to separate aikanes from alkenes, see for instance US Patent Application 14/334,605, US Provisional Applications 82/159,646, 62/159,668, and 62/262, 169 (now PCT applications
• Teflon® AF is AF 2400, which is reported to contain 83 mole percent PDD, and 17 mole percent tetrafluoroethylene.
• CF 2 CFOCF 2 CF(CF 3 )OCF 2 CF 2 S0 2 F, may also be employed, in copolymers of PDD with these alternative monomers, if is preferred that the PDD content be at least 90 mole percent.
• the sulfonic acid containing polymers that form the silver ionomers in the SL, and of course the ionomers themselves, are preferably fluorinated polymers, and more preferably 50% or more, very preferably 70% or more, and truly preferably 90% or more are carbon fluorine groups.
• this polymer is a perfluoropolymer, that is ail the monomer being polymerized to repeat unit contain no hydrogen.
• perfiuoropoiymers may have very small amounts of "adventitious" carbon hydrogen groups from impure monomers, or groups such as initiator fragments bonded to chains.
• this polymer is a perfluorinated polymer, that is all the monomer being polymerized to repeat unit contain no hydrogen.
• perfiuoropoiymers may have very small amounts of "adventitious" carbon hydrogen groups from impure monomers, or groups such as initiator fragments bonded to chains.
• the HDL layer is about 0.05 ⁇ to about 0.5 ⁇ thick, more preferably about 0.05 pm to about 0.2 ⁇ thick.
• Particularly preferred polymers for the HDL are copolymers of
• PDD perfluoro(2,2-methyl-1 ,3-dioxoole), particularly if included in a perfluoropolymer.
• PDD perfluoro(2,2-methyl-1 ,3-dioxoole),
• a preferred copolymer is that of PDD with tetrafluoroethylene, available as Teflon® AF (The Chemours Co., Wilmington, DE 19899, USA) and for further information about Teflon® AF, see P.R. Resnick, et a!., Teflon AF Amorphous
• Teflon® AF AF 2400, which is reported to contain 83 mole percent PDD, and 17 mole percent tetrafluoroethylene.
• Cytop® fluoropoiymer resin (reportedly a homopo!ymer f 1 , 1 ,2,4,4,5,5,6,7,7-deeaf1uoro-3-oxa-1-,6-heptadiene) available from Asahi Glass, 1-5-1 , arunouchi, Chiyoda-ku, Tokyo 100-8405, Japan, and Hyflon® DA-type fluoropoiymer resin, (reportedly a copolymer of tetrafluoroethylene and perfluoro(3-methoxy-1 ,3 ⁇ dioxoie) available from Solvay, SA, RUE DE RANSBEEK , 310, 120 Bruxeiles, Belgium.
• Cytop® fluoropoiymer resin (reportedly a homopo!ymer f 1 , 1 ,2,4,4,5,5,6,7,7-deeaf1uoro-3-oxa-1-,6-heptadiene) available
• the poiymer(s) in of the HDL are so-called "glassy" polymers.
• the polymer has no melting point above about 30°C with a heat of fusion of 3 J/g or more when measured by Differential Scanning calorimetry using AST Test
• a glassy polymer has a Glass Transition Temperature (Tg) above about 40°C,more preferably about 40°C.
• Tg Glass Transition Temperature
• the Tg is measured according to ASTM Test D3418- 12e1 at a heating and cooling rate of 10°C/min, and the Tg is taken as the midpoint (inflection point) of the transition on the second heat.
• the Tg is less than about 220°C, because for instance if the Tg is too high it may be difficult to dissolve the polymer to form a coating or layer.
• the polymers for the HDL may contain functional groups but preferably these functional groups are relatively difficult to oxidize and will not complex or react with the silver ion in the SL, Useful groups include perfluoroether and choro (particularly when present as chlorotrifiuoroethyiene). Groups which preferably are not present are primary and secondary alcohol, lodo, bromo, and aldehyde..
• the HDL has a permanence to nitrogen of at least 250 GPU at about 25°C
• this permanence should be at least about 500 GPU and more preferably at least about 1000 GPU, especially preferably about 1500 GPU, and very preferably at least about 2500 GPU, and most preferably at least about 5000 GPU.
• a relatively thick layer of the HDL material may be used, and this would support a membrane having only two layers, the HDL and SL.
• a third layer is added a (micro)porous layer, a layer containing many small pores through which the desired may flow relatively unobstructed, while the HDL is very thin so that the productivity of the TFC is high per unit area.
• This porous layer (PL) may be made thick enough to physically support the entire three (or more) layer TLC without sacrificing much productivity.
• the structure of the TLC in order of layers, is typically SL/HDL/PL (the slashes indicating where layer surfaces are laminated together)L, with the SL being exposed to the mixture from which one or more components is to be separated, and the separated product passing through the HDL and emerging from the "free surface” of the PL or vice versa in this type of configuration, the HDL is often termed the "gutter layer".
• this gutter layer often improves the throughput of the TLC per unit area of TLC, see M. Kattula, et a/., Designing uitrathin film composite membranes: the impact of a gutter iayer, Scientific Reports, 5, Article Number 15018 (2015), which is hereby included by reference.
• the gutter iayer has another unexpected effect, improving the separation of the TLC as a whole.
• materials usually polymers
• materials chosen for the various layers of a TLC are chosen partially because under the conditions the TLC will be used they are chemically and physically stable.
• the silver ionomers of the SL iayer are not very chemically stable, especially in the presence of organic compounds which can be relatively readily oxidized.
• Most materials for the PLs organic polymers which often contain small amounts of adventitious chemical materials or oxidizabie groups in the polymers themselves, which are oxidized by Ag + , the silver often being reduced the metal, and thereby becoming ineffective in separate ng alkanes from alkenes.
• fluoropolymers especially perfiuoropolymers, described herein for the HDL are effective in not only perhaps improving productivity of the membrane, but in the proper configuration help protect the integrity of the SL, improving its "separation properties" initially and over a longer period of time, see for instance Table 1 below.
• HDL high-density lipoprotein
• additional HDL Iayer may be present, preferably in the HDIJSIJHDL/PL configuration wherein the additional HDL iayer protects the "exposed" surface of the three iayer HDL with a SL/HDL/PL from contamination and perhaps degradation from materials in the mixture which is to be (partially) separated.
• additional HDL iayer protects the "exposed" surface of the three iayer HDL with a SL/HDL/PL from contamination and perhaps degradation from materials in the mixture which is to be (partially) separated.
• the HDL must have a minimum permeance to nitrogen at about 25°C of at least about 500 GPU, preferably at least about 1000 GPU, more preferably at least about 1500 GPU and very preferably at least about 2000.
• these layer are typically made out of polymers which have a high permeability to the gas being tested, in this instance nitrogen, and are generally quite thin, because the higher the thickness the lower the permeance.
• these SLs can be about 0.1 to about 1.0 ⁇ thick, preferably about 0.2 to about 0.5 ⁇ thick. It may be difficult to measure permeances on layer by themselves that are so thein because of damage from forming and handling such thin layers.
• the measurement of the permeance of the HDL can be measured with the HDL supported by a porous layer, the porous layer having a much higher "permeance" to the gas being tested than the HDL itself.
• a membrane having HDL layer, and for instance the porous layer are both made by the same process used to make the actual membrane which is to be used to the oiefin/alkane separation, see for instance the preparation of the as "Teflon AF/PAN" substrate in Example 3 below.
• GPU units herein have the units of (1x10 "6 ) sec/cm 2 s cm Hg, while permeability units are often in Barrer, which are (1x10 10 ) sec-cm/cm 2 -s cm H ethod of Measuring Nitrogen Permeance of the
• a 47 mm flat disc membrane containing only gutter layer material as a membrane on a porous support is punched from a larger 3 inch flat sheet membrane.
• the 47 mm disc is then placed in a stainless steel cross flow testing ceil comprised of a feed port, retentate port, a sweep inlet port, and a permeate port.
• Four hex bolts are used to tightly secure the membrane in the testing ceil with a total active area of 13.85 cm 2 .
• the feed port of the ceil is connected to a gas manifold consisting of 4 gases: nitrogen, oxygen, helium, and carbon dioxide.
• the retentate port is connected to a ball valve to dead end the gas flow as well as the purge the gas.
• One of the two permeate ports is shut and the other is connected to a flow meter.
• Nitrogen is brought up to pressure by a gas regulator and allowed to purge slowly for 1 minute.
• the retentate port is closed and a flow measurement can be taken from the permeate which is at atmospheric pressure. This process is repeated for three different feed pressures between 5 to 10 psig so that an average permeance can be calculated.
• the feed pressure, permeate fiowrate, and temperature are recorded for the calculation.
• the permeance can be calculated by the equation:
• the ceil was placed in a testing apparatus comprising of a feed line, a retentate line, a sweep line, and a permeate line.
• the feed consisted of a mixture of an olefin (propylene) gas and a paraffin (propane) gas.
• olefin propylene
• paraffin propane
• Each gas was supplied from a separate cylinder.
• polymer grade propylene 99.5 vol% purity
• paraffin 99.9 vol% purity propane was used.
• the two gases were then fed to their respective mass flow controllers where a mixture of any composition can be made.
• the standard mixing composition was 20 vol% oiefin and 80 mol% paraffin at a total gas flow rate of 200 mL/min.
• the mixed gas was fed through a water bubbler to humidify the gas mixture bringing the relative humidity to greater than 90%.
• a back pressure regulator is used in the retentate line to control the feed pressure to the membrane.
• the feed pressure was normally kept at 80 psig (0.41 MPa) after the back pressure regulator the gas is vented.
• the sweep line consisted of a pure humidified nitrogen stream. Nitrogen from a cylinder was connected to a mass flow controller. The mass flow controller was set to a flow of 300 mLJmin. The nitrogen was fed to a water bubbler to bring the relative humidity to greater than 90%. After the bubbler the nitrogen was fed to the sweep port of the membrane to carry any permeating gas through to the permeate port.
• the permeate line consisted of the permeated gas through the membrane and the sweep gas as well as water vapor.
• the permeate was connected to a three way valve so flow measurements could be taken.
• a Varian® 450 GC gas chromatograph (GC) with a GS-GasPro capillary column (0.32mm, 30m) was used to analyze the ratio of the olefin and paraffin in the permeate stream.
• the pressure in the permeate side was typically between 1.20 and 1.70 psig (8.3 to 1 1.7 kPa), but for Examples herein was 0.0 to 0.3 psig ("0" to 2.1 kPa). Experiments were carried out at room temperature.
• feed pressure permeate pressure
• temperature permeate pressure
• sweep-in flow rate nitrogen + water vapor
• total permeate flow rate permeate + nitrogen + water vapor
• PDD/VF/SEFVE terpolymer as a colorless solid (Tg 37 °C).
• the liquid was decanted and 80 mL of deionized water was added and then stirred for 30 minutes, After the liquid decanting, the water washing was repeated twice and the solid residue was dried in a vacuum oven at 60 °C for 3 hours. A brownish solid (2.7 g) containing free sulfonic acid groups was obtained.
• Solution 3 into a glass bottle, were added 0.5g of Nafion®D2020 (obtained from DuPont Fuel Cells, P.O. Box 80701 , Wilmington, DE, 19880-0701 , USA, and reportedly containing 20 weight percent polymer, about 34wt% of water, and about 46 wt. % of 1- propanol, 1.03-1.12 meq/ g of acid capacity on a polymer basis), 20mg of silver nitrate, 4.5g of isopropyl alcohol. The resulting solution was stirred for 1-2 hours, and then filtered through a glass fiber filter having a pore size of 1.2 ⁇ . This solution is denoted as "Solution 4".
• a substrate was prepared by coating a 0.2 weight % solution of Teflon® AF2400 (available from the DuPont Co, Wilmington, DE 19898, USA) (for further information about Teflon® AF, see P.R. Resnick, et ai., Teflon AF Amorphous Fluoropolymers, J. Schiers, Ed., Modern Fluoropolymers, John Wiley & Sons, New York, 1997, p. 397-420, which is hereby included by reference) in Fluorinert® 770 (available from 3 Corp., 3M Center, Sty.
• Another substrate was prepared by coating 10% Sylgard®184 in n-hexane on PAN350 membrane made. This substrate is denoted as PDMS/PAN.
• the Solution 1 was coated on directly PAN350 membrane and coated on Teflon AF/PAN respectively at ⁇ 30% relative humidity.
• the Solution 2 was coated on PAN350 membrane, coated on Teflon AF/PAN and coated on PDMS/PAN respectively at ⁇ 30% relative humidity.
• the Solution 3 was coated on PAN350 membrane, coated on Teflon AF/PAN and coated on PDMS/PAN respectively at ⁇ 30% relative humidity.
• the Solution 4 was coated on PAN350 membrane and coated on Teflon AF/PAN respectively at ⁇ 30% relative humidity.
• Obtained composite membranes are measured the propane and propylene permeances as following method.
• the permeance measurement membrane was a 47mm diameter, a fiat sheet.
• the feed gas composition, 20 mole % propylene (polymer synthesis grade), and 80% propane was humidified by passing it through a water bubbler.
• the total flow rate of both gases was 200 mLJmin.
• the feed gas (mixture of propylene and propane) was 60 psig, and the sweep gas on the second side of the membrane was humidified nitrogen at a pressure of 0.0 to 0.3 psig.
• the permeate from the second side of the membrane was analyzed by GC to determine the molar ratio of propane and propylene.
• Permeances (GPU) are given in cm 3 /cm 2 /sec/cm Hg x 10 6 .
• Table- 1 shows the permeance measurements result
• HFPO dimer peroxide solution (0.12 M) in Vertrei XF and 5 mL Vertre! XF. After degassing the mixture for 5 minutes with argon at 0 °C, the glass tube was sealed, allowed to warm to room temperature in a water bath and the reaction mixture is stirred overnight. The tube was opened to air and 30 mL acetone was added into the mixture.
• High Diffusion Rate Layer Permeability Measurements Solutions were prepared from Teflon® AF 2400 in Fluorinert®770 at various concentrations (Table 2) and coated on a PAN350 membrane as described in example 3. It is believed lower polymer concentration results in formation of thinner membranes. These supported membranes were tested for nitrogen permeance at feed pressures of 10, 20 and 30 psig (68.9, 137.8 and 207.7 kPa) and at ambient (atmospheric) pressure on the product side. The results shown in Table 2 for each solution are averages of the three feed pressures.

Landscapes

• Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Organic Chemistry (AREA)
• Health & Medical Sciences (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Engineering & Computer Science (AREA)
• Analytical Chemistry (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Materials Engineering (AREA)
• Water Supply & Treatment (AREA)
• General Chemical & Material Sciences (AREA)
• Wood Science & Technology (AREA)
• Life Sciences & Earth Sciences (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
• Separation Using Semi-Permeable Membranes (AREA)
• Laminated Bodies (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Priority Applications (5)

Applications Claiming Priority (6)

Publications (1)

Family

ID=57248230

Family Applications (4)

Family Applications After (3)

Country Status (6)

Cited By (3)

Families Citing this family (11)

Citations (4)

Family Cites Families (41)

• 2016
  • 2016-05-06 US US15/573,199 patent/US20180085714A1/en not_active Abandoned
  • 2016-05-06 US US15/573,436 patent/US20180093230A1/en not_active Abandoned
  • 2016-05-06 EP EP16793233.4A patent/EP3294782A1/en not_active Withdrawn
  • 2016-05-06 CN CN201680035437.6A patent/CN107683273B/zh active Active
  • 2016-05-06 EP EP16793237.5A patent/EP3294694A1/en not_active Withdrawn
  • 2016-05-06 JP JP2017558732A patent/JP2018519372A/ja active Pending
  • 2016-05-06 JP JP2017558731A patent/JP2018518561A/ja active Pending
  • 2016-05-06 WO PCT/US2016/031135 patent/WO2016182887A1/en not_active Ceased
  • 2016-05-06 US US15/573,287 patent/US20180111099A1/en not_active Abandoned
  • 2016-05-06 KR KR1020177035638A patent/KR20180008564A/ko not_active Ceased
  • 2016-05-06 CN CN201680037766.4A patent/CN107835797A/zh active Pending
  • 2016-05-06 CN CN201680032925.1A patent/CN107614549A/zh active Pending
  • 2016-05-06 CN CN201680032939.3A patent/CN107614466A/zh active Pending
  • 2016-05-06 WO PCT/US2016/031117 patent/WO2016182880A1/en not_active Ceased
  • 2016-05-06 EP EP16793238.3A patent/EP3294695B1/en active Active
  • 2016-05-06 WO PCT/US2016/031130 patent/WO2016182886A1/en not_active Ceased
  • 2016-05-06 WO PCT/US2016/031140 patent/WO2016182889A1/en not_active Ceased
  • 2016-05-06 KR KR1020177035568A patent/KR20180008559A/ko not_active Withdrawn
  • 2016-05-06 JP JP2017558719A patent/JP6774966B2/ja active Active
  • 2016-05-06 US US15/573,442 patent/US10399044B2/en active Active
  • 2016-05-06 EP EP16793240.9A patent/EP3294696A4/en not_active Withdrawn
  • 2016-05-06 KR KR1020177035637A patent/KR102118877B1/ko active Active

Patent Citations (4)

Non-Patent Citations (2)

Also Published As

Similar Documents

Legal Events