WO2001005492A1 - Polyvinylidene difluoride membranes and methods for making such membranes - Google Patents

Polyvinylidene difluoride membranes and methods for making such membranes Download PDF

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Publication number
WO2001005492A1
WO2001005492A1 PCT/US2000/016446 US0016446W WO0105492A1 WO 2001005492 A1 WO2001005492 A1 WO 2001005492A1 US 0016446 W US0016446 W US 0016446W WO 0105492 A1 WO0105492 A1 WO 0105492A1
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WIPO (PCT)
Prior art keywords
membrane
polyvinyl alcohol
approximately
membranes
alcohol
Prior art date
Application number
PCT/US2000/016446
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English (en)
French (fr)
Inventor
Shmuel Sternberg
Daniel R. Boggs
Robin G. Pauley
Bonny Moy
Original Assignee
Baxter International 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 Baxter International Inc filed Critical Baxter International Inc
Priority to EP00941430A priority Critical patent/EP1140334A1/en
Priority to AU56137/00A priority patent/AU5613700A/en
Priority to JP2001510571A priority patent/JP2003504190A/ja
Publication of WO2001005492A1 publication Critical patent/WO2001005492A1/en

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D67/00Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
    • B01D67/0081After-treatment of organic or inorganic membranes
    • B01D67/0088Physical treatment with compounds, e.g. swelling, coating or impregnation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D63/00Apparatus in general for separation processes using semi-permeable membranes
    • B01D63/16Rotary, reciprocated or vibrated modules
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D69/00Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
    • B01D69/02Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor characterised by their properties
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D71/00Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
    • B01D71/06Organic material
    • B01D71/30Polyalkenyl halides
    • B01D71/32Polyalkenyl halides containing fluorine atoms
    • B01D71/34Polyvinylidene fluoride

Definitions

  • the present invention relates generally to microporous, polyvinylidene difluoride (PVDF) membranes and to methods for making such membranes . More particularly, the present invention is directed to PVDF membranes (and the methods for making such membranes) that are hydrophilic and that retain their hydrophilic properties even after repeated wetting and drying.
  • PVDF polyvinylidene difluoride
  • PVDF membranes for liquid filtration are well known.
  • PVDF is inherently hydrophobic (lacking affinity for water) . Therefore, to use a PVDF membrane to filter aqueous fluid, the membrane must first be made hydrophilic (i.e., readily wet by water). To render it hydrophilic, PVDF is typically treated with a wetting agent or surfactant.
  • PVDF membranes One drawback with treated PVDF membranes is the possibility of extraction or leaching of the agent or surfactant from the membrane and into the filtrate during membrane use. This may be of particular, although not exclusive, concern where the PVDF membrane is used in the processing of a biological fluid (such as blood) which is intended for administration to a human. Extraction of the surfactant or wetting agent may also result in the loss of hydrophilicity and diminishes the efficiency or usefulness of the membrane as a filter for filtering aqueous solutions. Loss of hydrophilicity may also prevent reuse of the membrane.
  • PVDF membrane Although reuse may not be much of a concern where the membrane is part of a disposable fluid processing device (and only intended for one-time use) , such as in filters used in medical care or treatment, a reusable membrane may be desirable in other settings .
  • Methods have been developed for treating PVDF membranes to ensure that the surfactant or the wetting agent remains on the surface of the membrane and/or is not substantially extracted during use.
  • U.S. Patent No. 4,618,533 discloses a composite PVDF membrane.
  • the PVDF membrane is made, in part, by placing the membrane in a reagent bath that includes a free radical polymerizable monomer, a polymerization initiator and a cross-linking agent. A polymerization reaction is carried out which results in a porous membrane having a permanent hydrophilic coating grafted and/or deposited thereon.
  • U.S. Patent No. 5,032,331 discloses a process of impregnating the pores of a hydrophobic PVDF membrane with a solution that renders the pores of the PVDF membrane hydrophilic. After the impregnation step, the PVDF membrane is subjected to a chemical treatment in a strong alkali solution containing an oxidizing agent. According to the patent, the membrane, thus treated, exhibits "semi-permanent hydrophilicity and could be dried and used cyclically.”
  • a microporous membrane that includes (1) a porous layer of polyvinylidene difluoride (PVDF) and (2) a polyvinyl alcohol coating on the PVDF layer, sufficient to render it hydrophilic.
  • PVDF polyvinylidene difluoride
  • the membrane is rewettable by an aqueous liquid after drying and is not cross-linked or contacted with a strong alkali solution. Yet it remains substantially rewettable, even after repeated wetting and drying .
  • such a membrane remains hydrophilic even after exposure or contact with an aqueous liquid as hot as 40°C and conceivably as hot as approximately 100°C.
  • the polyvinyl alcohol coating solution comprises approximately 1-2%, by weight, of polyvinyl alcohol dissolved in a solution of water and alcohol, such as isopropyl alcohol.
  • the solution may include 20-80% water and 20-80% isopropyl alcohol, by weight.
  • the polyvinyl alcohol is derived from polyvinyl acetate having a degree of saponification between about 80-100%.
  • the present invention is directed to a method for making a microporous, non-crosslinked, rewettable, hydrophilic PVDF membrane.
  • the method includes providing a porous, dry, hydrophobic PVDF membrane and contacting the membrane with a coating solution.
  • the coating solution is made from polyvinyl alcohol dissolved in a solution of water and alcohol.
  • the coating solution is provided by dissolving the polyvinyl alcohol in a solution of water and alcohol, such as isopropyl alcohol.
  • the solution may include 20-80% water and 20-80% isopropyl alcohol, by weight.
  • the membrane may be coated by immersing the PVDF membrane in a bath of the polyvinyl alcohol coating solution.
  • the present invention is directed to an apparatus for separating a biological fluid into two or more components.
  • the apparatus includes a housing comprising an interior wall defining a fluid chamber, a fluid inlet and at least one fluid outlet which communicate with the chamber.
  • the apparatus also includes a rotor within the chamber and a microporous membrane disposed on either one of the interior wall or the rotor.
  • the membrane is made of a porous layer of polyvinylidine difluoride and a polyvinyl alcohol coating thereon sufficient to render the polyvinylidene difluoride layer hydrophilic.
  • Figure 1 is a cross-sectional view of a membrane embodying the present invention without an internal support ,-
  • Figure 1A is a cross sectional view of another membrane embodying the present invention with an internal support
  • FIG. 2 is a diagram showing the method of making PVDF membranes in accordance with the present invention.
  • Figure 3 is a perspective view of a separation device incorporating a PVDF membrane embodying the present invention, with a portion of the device broken away to show the device interior.
  • Membranes of the present invention may be flat sheet, porous membranes.
  • a membrane 10 embodying the present invention is generally depicted in Fig. 1.
  • Membrane 10 typically includes one or more layers of a polymeric material that includes polyvinylidene difluoride (PVDF) .
  • the layers may be made entirely of PVDF or may be made of a blend of PVDF and other suitable polymers and copolymers .
  • PVDF membrane or “PVDF layer” encompasses membranes or layers made entirely of PVDF and/or blends of PVDF with other polymers and/or copolymers.
  • the surfaces 11 of PVDF membrane are typically treated with a hydrophilic coating.
  • PVDF membranes are coated with a wetting agent such as polyvinyl alcohol .
  • the membrane 10 may be used in association with an internal support 18, typically made of a fibrous, porous polymeric material such as polyester mesh, onto which one or more layers of PVDF is applied to form the PVDF membrane .
  • an internal support 18 typically made of a fibrous, porous polymeric material such as polyester mesh, onto which one or more layers of PVDF is applied to form the PVDF membrane .
  • membranes may have a thickness of approximately 4-7 mils or approximately .004 -.007 inches.
  • the membranes are substantially isotropic but may also be anisotropic (i.e., where the pore size changes from one surface of the membrane to the other) .
  • Membranes made in accordance with the present invention may be "microporous" membranes, having a nominal pore size of less than about 100 microns and typically between approximately 0.01-10 microns.
  • membranes made in accordance with the present invention may be "ultrafiltration" membranes, having a nominal pore size of less than approximately 0.01 microns and/or are suitable for the filtration of, for example, dissolved proteins.
  • the microporous membrane may have a nominal pore size of approximately 0.2-1.2 microns. More typically, the nominal pore size of the membrane may be no less than approximately 0.8 microns .
  • PVDF is available from many different sources such as Elf Atochem of Philadelphia, Pennsylvania.
  • the PVDF prior to forming the membrane, the PVDF is typically dissolved in a suitable solvent.
  • a suitable solvent for PVDF is dimethylacetamide (DMAC) .
  • DMAC dimethylacetamide
  • approximately 18-22%, by weight, of PVDF is dissolved in DMAC to provide a PVDF solution.
  • this PVDF solution is maintained (“cured") for approximately 18 hours at between 28-35°C and more preferably, approximately 31°C prior to forming the membrane.
  • DMAC dimethylacetamide
  • this PVDF solution is maintained (“cured") for approximately 18 hours at between 28-35°C and more preferably, approximately 31°C prior to forming the membrane.
  • different solvents, different curing times and temperatures may be used.
  • FIG. 2 illustrates one method and the associated apparatus for making a membrane of the present invention.
  • the method depicted in Fig. 2 is commonly known as a flow-casting method in which the membrane is formed continuously on a moving support surface such as a web or belt made of a suitable material.
  • a flow-casting method in which the membrane is formed continuously on a moving support surface such as a web or belt made of a suitable material.
  • the present invention is not limited to the particular method employed in making the membrane or the presence or absence of a support surface .
  • PVDF membranes without the support as shown in Fig . 1 , may be made by applying the PVDF to a drum and thereafter peeling the membrane off the surface of the drum.
  • PVDF membranes may be made by casting a PVDF solution onto a support of the type described above, forming the membrane and then separating the membrane from the support, as described in U.S. Patent No. 4,203,848, which is incorporated by reference herein.
  • the web or support 18 is dispensed from supply roll 22 into a V-shaped trough or chamber 24 that is filled with the cured PVDF solution 25 (described above) .
  • the PVDF solution is applied to the outer surfaces of the support web 18.
  • apparatus includes a series of rollers 36 over which the support is threaded as generally shown. Rotation of rollers 36 effects movement of the support 18 from dispenser 22 through the series of baths and drying devices, which are described in more detail below.
  • the rate of movement of support 18 may depend on the required or desired residence times of the support (with the membrane applied thereon) within the baths and drying devices. In one embodiment, the rate of movement may be between approximately 1-5 ft/min and, more typically, approximately 3 ft/min.
  • the coated support 18 then passes through a first coagulation bath 26.
  • the first coagulation bath 26 holds a liquid or solution which is a non-solvent for the polymer (e.g., PVDF) portion of the PVDF solution, but is freely miscible with the solvent portion (e.g., DMAC) of the PVDF solution.
  • the solvent portion e.g., DMAC
  • Contact with the liquid in the coagulation bath 26 coagulates the polymer solids (PVDF) and extracts the solvent portion (i.e., DMAC) from the applied layer of PVDF, thereby forming a porous PVDF membrane on the support.
  • This "solvent/non solvent” method of forming membranes is well known to those of skill in the art and is described in, for example, U.S. Patent No. 3,642,668, which is incorporated by reference herein.
  • the support 18 with the PVDF membrane on its surface is then advanced from coagulation bath 26 to one or more extraction baths 28.
  • the extraction bath(s) will contain a liquid that extracts any residual solvent
  • the liquid may be water.
  • the membrane may undergo a series of wash steps in one or more extraction baths 28, each bath further washing and removing solvent from the membrane .
  • three extraction baths 28 are shown in Fig. 2.
  • the membrane is dried.
  • Various drying techniques may be used. For example, after the final extraction bath, the membrane may be introduced into a drying oven 40 shown in Fig. 2. Alternatively, and perhaps more preferably, the membrane may be dried by contacting the membrane sheet with one or more heated drums, which dry the membrane in a manner well understood by those of skill in the art.
  • a drying temperature of approximately 65°C or less may be sufficient to thoroughly dry the membrane.
  • the temperature of the first drum may be higher than the temperature of the later drums in the series to allow substantially all of the water to be evaporated from the wet membrane.
  • the later drums which are set at a lower temperature (such as, but not limited to, 50°C to 60°C) , ensure that the membrane is completely dry.
  • excess water may also be removed from the membrane by passing the membrane between wipers 41 prior to drying, as generally depicted in Fig. 2.
  • the membrane After the membrane is dried, it must be further treated by coating the membrane surface with a wetting agent to make it hydrophilic.
  • the membrane after drying, the membrane may be introduced into another bath 44 containing a hydrophilic coating solution.
  • the method of coating is not limited to immersing the membrane in the coating solution, but may also include spraying or other forms of applying the wetting agent to the membrane.
  • the wetting agent is polyvinyl alcohol which has been dissolved in a solution of water and isopropyl alcohol.
  • Polyvinyl alcohol is derived from saponified polyvinyl acetate. (Saponification refers to the process of hydrolyzing an ester) .
  • Polyvinyl alcohol is available in a variety of grades, according to the degree of saponification. In the PVDF membranes of the present invention, polyvinyl alcohol having a degree of saponification of at least about 40% may be used.
  • Polyvinyl alcohol having a high degree of saponification, for example, greater than 80% is, however, preferred.
  • the polyvinyl alcohol coating solution may be prepared as follows.
  • Highly saponified polyvinyl alcohol is typically dissolved in hot water, such as water having a temperature of approximately 90°C.
  • the dissolved polyvinyl alcohol is then further mixed with another alcohol to provide the coating solution.
  • the coating solution includes approximately 20-80% water and 20-80% of the other alcohol, and more preferably, 40% to 60% water and 40% to 60% of the other alcohol.
  • One particularly useful alcohol for the coating solution is isopropyl alcohol.
  • Other simple alcohols, such as methanol, may also be suitable.
  • the coating solution may include approximately 50% water and 50% isopropyl alcohol.
  • the polyvinyl alcohol is dissolved in the solution to provide a coating solution having approximately 0.1% to 10%, by weight, polyvinyl alcohol.
  • the concentration of polyvinyl alcohol in the coating solution is approximately 1-10 % and more preferably, approximately 1-2%, by weight.
  • a less saponified polyvinyl alcohol may be used, such as polyvinyl alcohol having a degree of saponification of at least about 40% but less than approximately 80%.
  • the polyvinyl alcohol may first be dissolved in an alcohol such as isopropyl alcohol. Water may be added to achieve the water/alcohol ratios described above.
  • the less saponified polyvinyl alcohol may be dissolved in a mixture of alcohol and water.
  • the level of liquid 45 in the coating solution bath 44 be such that the membrane enters the bath 44 at a point where it is not in contact with a roller 36. This allows for better displacement of air by the coating solution, which results in improved and/or more uniform wetting of the membrane.
  • the membrane may be further dried in another drying apparatus such as oven 48, which dries the membrane as described above in connection with the PVDF membrane prior to wetting. After drying, the membrane may be cut (to its desired width) and accumulated on take-up roll 50. The membrane may be further cut into smaller lengths or widths as necessary.
  • Membranes made in accordance with the present invention may have many different uses. For example, the membranes of the present invention may be used wherever a component or particle must be separated from the liquid in which it is suspended. In one specific embodiment, membranes made in accordance with the present invention may be used in a disposable processing set for separating a biological fluid such as blood into its components.
  • whole blood may be passed through the membrane to separate the whole blood into plasma, on the one hand, and concentrated blood cells (such as red cells and white cells) , on the other hand.
  • concentrated blood cells such as red cells and white cells
  • An example of a separation device or separator with which the membrane of the present invention may be used is described in more detail below.
  • the separation device is only one example of possible uses for the membrane, and nothing in the description that follows should be construed as limiting the present invention to use with such a device.
  • membranes made in accordance with the present invention may be used in laboratory or industrial settings where the membrane is not limited to one time use, but rather may be repeatedly used.
  • a separator 60 that includes a PVDF membrane made in accordance with the present invention is shown in Fig.3.
  • Separator 60 is typically part of a disposable fluid processing used in association with a device for separating whole blood into plasma and concentrated blood cells, such as the Autopheresis-C ® plasmapheresis device marketed by Baxter Healthcare Corporation.
  • the structure and operation of the plasmapheresis device, including separator 60, are set forth in detail in U.S. Patent No. 5,194,145, incorporated by reference herein, and a detailed description will not be repeated here.
  • separator 60 includes a housing 66 defining a generally cylindrical inside surface 70.
  • the housing includes a fluid inlet 72, a first outlet 74 and second outlet 76.
  • a rotor 78 with a generally cylindrical outer surface, is rotatably mounted in the housing with the outer surface of the rotor spaced from the interior surface of the housing to define a small gap 82 therebetween.
  • the membrane 10 of the present invention is mounted on the rotor, with the membrane facing gap 82 located between rotor 78 and housing 66. The membrane rests atop a series of spaced- apart support ribs 86 on the surface of the rotor. These raised support ribs support the membrane and form channels to collect filtrate passing through membrane 10.
  • the membrane is shown on the surface of the rotor in Figure 3, alternatively, the membrane may be mounted on the generally cylindrical interior surface of the housing. In that event, the surface of the housing may similarly include raised ribs to support filter membrane and to collect filtrate passing through the membrane .
  • fluid such as a biological suspension or blood is introduced through inlet 72 and flows down through the gap 82 between the outer surface of the rotor 78 and inner surface of the housing 66. During the passage through the gap, the high-speed rotation of rotor generates turbulence in the form of Taylor vortices, which sweep the membrane free of clotting cells or debris.
  • plasma from the blood passes through membrane 10 and is collected in the channels defined between the spaced apart raised ribs.
  • the plasma flows down through the channels into a collection manifold, and passes through first outlet 74.
  • the remaining portion of the fluid or suspension e.g., concentrated cells is withdrawn from the housing through the second outlet 76.
  • Membranes made in accordance with the present invention are useful in the processing of blood as substantially described above in that they are biologically compatible with biological fluid, such as blood.
  • Membranes of the present invention are particularly well-suited for sonic welding to the rotors of the type described above.
  • PVDF is capable of forming alloys, during sonic welding, with the acrylic material typically used to make such rotors. This provides improved adhesion of the membrane to the rotor, resulting in improved quality and reliability of the separator and a reduced scrap rate .
  • PVDF membranes of the present invention are sterilizable by radiation sterilization such as gamma radiation or electron beam radiation.
  • An additional advantage of PVDF membranes made in accordance with the present invention, particularly when used to separate plasma from whole blood, is relatively minimal complement and platelet activation.
  • Complements are naturally occurring soluble proteins found in blood plasma that provide immune protection. They circulate throughout the body and become activated on exposure to an antigen and/or in the response to tissue injury. However, in some instances, the complement may become activated in the absence of activating antigen, such as by contact with the equipment used in the processing of blood. Since these complements are essential to the immune response in humans, it is desirable that complement activation during blood processing be kept to a minimum.
  • Platelets are essential in the repair of injured body tissue in that they help form clots and prevent excess bleeding. However, platelets may also become activated by contact with the equipment used in the processing of blood, including the membranes used for separating the blood components. Accordingly, it is also desirable that platelet activation be kept to a minimum.
  • the blood was separated into plasma and concentrated cells. Samples of the donor's blood were taken before and after the separation procedure. Samples of the collected plasma and concentrated cells (CCC) were also taken. The samples were assayed for complement activation and platelet activation.
  • membranes of the present invention have been described above in the context of and as part of a one time use disposable processing set for blood and blood components, membranes of the present invention may also be used in other settings where reusability of the membranes is desired. For example, it has been observed that membranes made in accordance with the present invention remain hydrophilic even after repeated use. Stated differently, membranes of the present invention are capable of being "rewet” after such use, and after drying. As used herein, “rewet” or “rewettable” refers to the ability of a membrane that has been previously wet and dried to substantially absorb a contacting aqueous liquid (i.e., without the presence of any dry spots) in less than about 1 minute.
  • the membranes of the present invention remain hydrophilic even though they are "non- crosslinked. " Although, it is possible that a small amount of cross-linking may occur during manufacture of the membrane, it will be understood that such minimal and incidental cross-linking is within the meaning of "non- crosslinked” , as that term is used herein.
  • Membranes made in accordance with the present invention were wet, dried and rewet with an aqueous liquid to demonstrate the rewetability of such membranes. The tests and results thereof are described below. EXAMPLE 1 PVDF membranes treated with 1% PVOH in the manner set forth above were placed into a Gelman filtration funnel and approximately 600 ml of room temperature water was passed through the membrane.
  • the membrane was then dried at 70°C for approximately 5 minutes and then contacted with a 0.9% saline solution. It was observed that the membrane rewet immediately.
  • the same membrane was then again placed into a funnel and approximately 800 ml of water at 40°C was filtered through the membrane. The membrane was dried and after drying, contacted with 0.9% saline. It was observed that the membrane rewet immediately.
  • PVDF membranes that have been prepared by the same process described above, but treated with other known wetting agents, such as polyethyleneglycol (PEG) .
  • PVDF membranes rendered hydrophilic with a 5% PEG coating solution (dissolved in water and isopropyl alcohol) wet initially, but did not rewet after drying.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)
  • External Artificial Organs (AREA)
PCT/US2000/016446 1999-07-16 2000-06-15 Polyvinylidene difluoride membranes and methods for making such membranes WO2001005492A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP00941430A EP1140334A1 (en) 1999-07-16 2000-06-15 Polyvinylidene difluoride membranes and methods for making such membranes
AU56137/00A AU5613700A (en) 1999-07-16 2000-06-15 Polyvinylidene difluoride membranes and methods for making such membranes
JP2001510571A JP2003504190A (ja) 1999-07-16 2000-06-15 ポリビニリデンジフルオリド膜およびこのような膜を作製するための方法

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US35622299A 1999-07-16 1999-07-16
US09/356,222 1999-07-16

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WO2001005492A1 true WO2001005492A1 (en) 2001-01-25

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JP (1) JP2003504190A (zh)
CN (1) CN1317987A (zh)
AU (1) AU5613700A (zh)
WO (1) WO2001005492A1 (zh)

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EP1440727A1 (en) * 2003-01-20 2004-07-28 Special Membrane Technologies, Inc. Membrane flux enhancement
EP1654053A1 (en) * 2003-07-08 2006-05-10 U.S. Filter Wastewater Group, Inc. Membrane post treatment
US7140496B2 (en) 2001-08-01 2006-11-28 Asahi Kasei Medical Co., Ltd. Multilayer microporous membrane
EP1776996A1 (en) * 2004-06-28 2007-04-25 Kureha Corporation Porous membrane for water treatment and process for producing the same
WO2007057057A1 (en) * 2005-05-09 2007-05-24 Mabtech Ab Pvdf membranes
US7459085B2 (en) 2002-10-18 2008-12-02 Asahi Kasei Medical Co., Ltd. Microporous hydrophilic membrane
US7635513B1 (en) 1999-10-22 2009-12-22 Asahi Kasei Medical Co., Ltd. Heat resistant microporous film
AU2004253197B2 (en) * 2003-07-08 2010-05-27 Evoqua Water Technologies Llc Membrane post treatment
EP2270485A1 (en) * 2008-04-04 2011-01-05 National Institute of Advanced Industrial Science and Technology Support for electrophoresis including hydrophobic polymer membrane, and migration separation method using the same
US9415350B2 (en) 2008-06-30 2016-08-16 3M Innovative Properties Company Method of forming a rewettable asymmetric membrane
EP3187248A3 (en) * 2015-12-28 2017-10-04 Fenwal, Inc. Membrane separation device having improved filtration velocity
US11511235B2 (en) * 2016-05-31 2022-11-29 Amogreentech Co., Ltd. Filter assembly, method for manufacturing same, and filter module comprising same

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US8079574B2 (en) * 2007-05-16 2011-12-20 ZenPure Corp. Membrane based contactor module for mass and heat transfer
KR101240194B1 (ko) 2010-06-03 2013-03-06 인하대학교 산학협력단 지질 이중막의 제조방법
US9643130B2 (en) * 2015-03-31 2017-05-09 Pall Corporation Hydrophilically modified fluorinated membrane (IV)

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Cited By (18)

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JP2003504190A (ja) 2003-02-04
AU5613700A (en) 2001-02-05
EP1140334A1 (en) 2001-10-10

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