USRE34828E - Immobilized-interface solute-transfer apparatus - Google Patents

Immobilized-interface solute-transfer apparatus Download PDF

Info

Publication number
USRE34828E
USRE34828E US07/781,864 US78186491A USRE34828E US RE34828 E USRE34828 E US RE34828E US 78186491 A US78186491 A US 78186491A US RE34828 E USRE34828 E US RE34828E
Authority
US
United States
Prior art keywords
extractant
solute
feed
liquid
solution
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
Application number
US07/781,864
Inventor
Kamalesh Sirkar
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Stevens Institute of Technology
Original Assignee
Stevens Institute of Technology
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 Stevens Institute of Technology filed Critical Stevens Institute of Technology
Priority to US07/781,864 priority Critical patent/USRE34828E/en
Application granted granted Critical
Publication of USRE34828E publication Critical patent/USRE34828E/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D61/00Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
    • B01D61/24Dialysis ; Membrane extraction
    • B01D61/246Membrane extraction
    • B01D61/2461Membrane extraction comprising multiple membrane extraction steps
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D11/00Solvent extraction
    • B01D11/04Solvent extraction of solutions which are liquid
    • B01D11/0415Solvent extraction of solutions which are liquid in combination with membranes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D61/00Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
    • B01D61/24Dialysis ; Membrane extraction
    • B01D61/28Apparatus therefor
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D61/00Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
    • B01D61/24Dialysis ; Membrane extraction
    • B01D61/32Controlling or regulating
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D63/00Apparatus in general for separation processes using semi-permeable membranes
    • B01D63/02Hollow fibre modules
    • B01D63/04Hollow fibre modules comprising multiple hollow fibre assemblies
    • B01D63/043Hollow fibre modules comprising multiple hollow fibre assemblies with separate tube sheets
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2313/00Details relating to membrane modules or apparatus
    • B01D2313/50Specific extra tanks
    • B01D2313/501Permeate storage tanks

Definitions

  • the present invention relates to a process for transferring solute from a liquid feed solution to a liquid extractant which is substantially immiscible with the feed solution.
  • Liquid-liquid extractions are often used in chemical processes to transfer a solute dissolved in a first liquid to a second liquid which is essentially immiscible with the first liquid.
  • the solution of the solute in the first liquid is generally termed a feed solution and the second liquid is generally termed an extractant.
  • the undissolved solute can be a solid, a liquid, or a gas.
  • the solute tends to distribute itself between the two liquids in accordance with the relative solubility of the solute in the two liquids. Since the feed solution and the liquid extractant are essentially immiscible, they form two distinct thermodynamic phases when in contact with one another. These two phases can be physically separated from one another, which effects a separation of a fraction of the solute from the feed solution.
  • the feed solution and the extractant are typically mixed together intimately.
  • intimate mixing frequently gives rise to troublesome problems.
  • the mixing generally involves forming a dispersion of one of (the liquids in the other. Frequently, the resulting dispersion is relatively stable, so that it takes a long time for the dispersed liquid to coalesce.
  • the throughput of the solute-transfer process is undesirably low or the inventory of feed solution and extractant tied up in the process is undesirably high.
  • U.S. Pat. No. 3,956,112 to Lee et al. refers to an extraction process in which a porous membrane serves as a partition between two immiscible solvents. Solutes from one solvent are transferred to the other solvent via direct solvent-solvent contact by way of the porous membrane.
  • conventional extraction processes in which immiscible solvents are separated by a porous membrane generally do not prevent one solvent from forming a dispersion in the other. Typically one or the other solvent seeps through the porous membrane and becomes dispersed in the solvent on the other side of the membrane.
  • the process of the invention involves transferring solute from a feed solution to a liquid extractant through a porous membrane.
  • the solute may be a solid, a liquid, or a gas.
  • the feed solution and the extractant when in direct contact with each other, are essentially immiscible with each other.
  • the process of the invention includes the step of contacting a first side of the porous membrane with the feed solution containing the solute and contacting a second, opposing side of the membrane with the liquid extractant.
  • the feed solution and the extractant can come into contact through the pores of the membrane.
  • On the surface of the porous membrane either the feed solution tends to displace the extractant or the extractant tends to displace the feed solution.
  • the fluid which tends to displace the other defines a membrane-wetting liquid.
  • the process further includes the step of maintaining an interface-immobilizing pressure difference between the feed solution and the extractant.
  • the interface-immobilizing pressure difference is imposed in a direction and a magnitude which is effective to substantially prevent the membrane-wetting liquid from flowing through the membrane and dispersing in the liquid on the opposite side of the membrane.
  • the interface between the feed solution and the extractant is thereby effectively immobilized at the porous membrane.
  • the effective diameters of the pores of the porous membrane should be sufficiently large to permit a flow of the membrane-wetting liquid through the pores and sufficiently large to permit the solute to pass through the pores.
  • the membrane should be mechanically strong enough--with suitable reinforcement, if necessary--to withstand the interface-immobilizing pressure difference imposed across the membrane under the intended operating conditions.
  • the membrane material may swell in the presence of the feed solution or the extractant. So long as the swollen membrane remains strong enough to withstand the interface-immobilizing pressure difference, the swelling of the membrane should not be a disadvantage.
  • the interface-immobilizing pressure difference should be imposed in a direction to oppose the tendency of the membrane-wetting liquid to pass through the membrane.
  • a greater pressure is imposed on the liquid opposite to the membrane-wetting liquid than is imposed on the membrane-wetting liquid in order to oppose the tendency of the membrane-wetting liquid to pass through the membrane.
  • the range of differences in pressure effective to immobilize the interface between a particular feed solution and extractant at a particular porous membrane depends on a number of factors, including the relative tendency of the feed solution and the extractant to wet the membrane material, the interfacial tension between the feed solution and the extractant, the flow characteristics of each liquid at the surface of the membrane, and the effective diameters of the pores of the membrane.
  • the minimum value of the pressure difference effective to immobilize the interface between the feed solution and the extractant at the porous membrane cannot in general be predicted a priori, largely because the formation of a dispersion depends strongly on the pattern of flow of the liquids at the surface of the membrane.
  • the average minimum pressure difference opposing the tendency of the membrane-wetting liquid to pass through the membrane should at least be greater than any pressure-difference fluctuations in the opposite direction which, for example, might be expected to be caused by pumping irregularities.
  • the smaller the pores of the membrane and the greater the interfacial tension between the feed solution and the extractant the greater is the maximum pressure difference which is effective to immobilize the interface.
  • a pressure difference range of from about 5 kPa to about 620 kPa has been found to be suitable for certain applications, with the range of from about 140 kPa to about 410 kPa being particularly preferred.
  • a membrane solute transfer unit for carrying out solute-transfer processes such as the process of the invention includes a porous membrane located within a liquid-tight housing.
  • the porous membrane divides the interior of the housing into two chambers: a feed solution chamber and an extractant chamber. Pores of the membrane provide communication between the two chambers.
  • the housing is provided with inlet and outlet ports which permit feed solution to be introduced and discharged from the feed solution chamber and liquid extractant to be introduced and discharged from the extractant chamber.
  • the solute-transfer unit of the invention also includes a mechanism for controlling the difference between the liquid pressure of feed solution in the feed solution chamber and the liquid pressure of the extractant in the extractant chamber.
  • the pressure difference is controlled so that it falls within a pressure range effective substantially to immobilize an interface between of the feed solution and the extractant at the porous membrane.
  • the porous membranes of the present invention may be hydrophilic or hydrophobic.
  • Preferred hydrophilic membranes include porous regenerated cellulose, porous cellulose acetate, porous cellulose acetate-nitrate, porous cellulose triacetate, microporous glass, and porous porcelain.
  • Preferred hydrophobic membranes include porous polyethylene, porous polypropylene, and porous polytetrafluoroethylene (PFTE).
  • the effective diameters of the pores of the membrane preferably lie in the range of from about 1 nm to about 10 ⁇ m.
  • the porous membrane should be as thin as is consistent with the need to be strong enough to withstand the interface-immobilizing pressure difference applied across the membrane. Porous membranes from about 25 ⁇ m to about 125 ⁇ m in thickness are preferred.
  • the porous membrane For solute-transfer processes carried out on an industrial scale, it is preferred for the porous membrane to be in the form of hollow tubular fibers with porous walls. Bundles of large numbers of such tubular fibers can provide a high value for the ratio of the area of porous membrane through which the solute transfer occurs to the volume of the vessel which contains the feed solution/membrane/extractant system. It is ordinarily preferred for the liquid which preferentially wets the porous wall of the tubular fiber to be located within the lumen of the fiber, since in that case the interface-immobilizing pressure difference would be directed from the outside of the tubular fiber to the inside of the fiber, thereby tending to compress the tubular wall of the fiber.
  • the walls of tubular fibers are stronger in compression than in tension.
  • the walls of the tubular fibers are sufficiently thick relative to the diameter of the tube to permit the tube to withstand a compressive interface-immobilizing pressure difference without collapsing.
  • a compressive interface-immobilizing pressure difference without collapsing.
  • a preferred double-transfer solute-transfer unit includes a liquid-tight housing, the interior of which is divided by two porous membranes into a sequence of three side-by-side chambers.
  • a feed solution could be pumped through a first end chamber.
  • An intermediate chamber separated from the first end chamber by a first porous membrane could contain an intermediate extractant liquid substantially immisible with the feed solution.
  • a second end chamber separated from the intermediate chamber by a second porous membrane could have pumped through it a back-extractant liquid which is immisible with the intermediate extractant.
  • the back-extractant liquid could be completely miscible with the feed solution, if desired.
  • Solute in the feed solution in the first chamber could be transferred to the intermediate extractant in the intermediate chamber through the first porous membrane.
  • the solute could then diffuse through the intermediate extractant to the second porous membrane and then be transferred to the back extractant through the second membrane.
  • the intermediate chamber preferably is as narrow as practical to minimize the diffusion path length and to minimize the inventory of intermediate extractant and solute held up in the intermediate chamber.
  • a first interface-immobilizing pressure difference should be maintained across the first membrane to oppose the tendency of the feed solution or the intermediate extractant, as the case may be, to pass through the membrane.
  • a second interface-immobilizing pressure difference should be maintained across the second membrane to oppose the tendency of the intermediate extractant or the back extractant, as the case may be, to pass through the membrane.
  • a feed solution could be pumped through the intermediate chamber of the preferred double-transfer solute-transfer unit discussed in the preceding paragraph.
  • First and second extractant liquids each immiscible with the feed solution, could be pumped through the first and second end chambers.
  • An interface-immobilizing pressure difference should then be maintained across each of the first and the second porous membrane to oppose the tendency of one or the other of the feed solution or extractant liquid to pass through the membrane.
  • a preferred double-transfer extraction cell includes two bundles of hollow tubular fibers with porous walls passing through the interior of a liquid-tight housing.
  • the feed solution is pumped through the first bundle of tubular fibers and the back extractant is pumped through the second bundle of tubular fibers.
  • the intermediate extractant fills the interior of the housing, exterior of the tubular fibers.
  • the fibers of the two bundles are preferably commingled and located close to one another to reduce the diffusion path length from the fibers containing the feed solution to the fibers containing the back extractant.
  • the mechanism for maintaining an interface-immobilizing pressure difference across a porous membrane in the process of the invention may be a closed-loop feed back-type pressure regulating system, if desired.
  • a preferred closed-loop pressure regulating system would sense the liquid pressure on both sides of the porous membrane and control the fluid pressure on one side or the other to maintain the difference between the pressures to within a preset range.
  • the mechanism for maintaining an interface-immobilizing pressure difference across the porous membrane could be an open loop pressure regulating system.
  • the liquid pressure on a first side of the membrane is maintained at a first preset value and a liquid pressure on the opposite side of the membrane is maintained at a second preset value essentially independently of the pressure on the first side.
  • the two preset values are chosen so that the difference between the pressure on the two sides falls within a desired interface-immobilizing pressure range.
  • fermentation products can be continuously withdrawn from an aqueous fermentation broth as the fermentation proceeds by transfer to an organic solvent which is immiscible with water.
  • Ethyl alcohol could be extracted from such a broth by a solvent such as dibutyl phthalate or tributyl phosphate separated from the broth by a membrane of porous polypropylene. Cellular debris and other particulate matter in the broth would be prevented from contaminating the solvent stream by the porous membrane.
  • Antibiotics or other fermentation products could be extracted from the broth in an analogous manner with appropriate extractant liquids.
  • Oxygen could be introduced into and carbon dioxide withdrawn from the fermentation broth using a gas-permeable membrane at the same time as fermentation products were being extracted using the process of the invention.
  • the process of the invention could also be used to separate phenol from waste water using MIBK or diisopropylether as an extractant. If the waste water contained hydrogen sulfide or ammonia in addition to phenol, the MIBK or diisopropylether extractant could be used to extract the phenol and the hydrogen sulfide or ammonia could be removed simultaneously using a gas-permeable membrane. Aromatics could be extracted from petroleum distillates using sulfolane or propylene carbonate as an extractant. Other applications of the solute-transfer process of the invention will occur to persons skilled in the art.
  • FIG. 1 is a schematic diagram of a first preferred membrane solute-transfer unit.
  • FIG. 2 is a schematic diagram of a second preferred membrane solute-transfer unit which employs an intermediate extractant.
  • FIG. 3 is a schematic diagram of a third preferred membrane solute-transfer unit which employs porous membranes in the form of hollow tubes.
  • FIG. 4 is a schematic diagram of a fourth preferred membrane solute-transfer unit which employs porous membranes in the form of hollow tubes.
  • a membrane solute-transfer unit 2 includes an extraction cell 3 which has a porous membrane 4 located within a housing 6.
  • the membrane 4 is sealed to the walls of the housing 6 and divides the interior of the housing into a feed solution chamber 8 and a liquid extractant chamber 10. Pores passing through the membrane 4 provide communication between the feed solution chamber 8 and the extractant chamber 10.
  • a reinforcing screen 12 is adjacent to the porous membrane 4 on the side of the membrane facing the extractant chamber 10. The screen 12 provides mechanical support for the membrane 4.
  • a feed-solution inlet port 14 and a feed-solution outlet port 16 permits a feed solution to be introduced into and discharged from the feed solution chamber 8.
  • a feed-solution pump 22 is connected to the feed-solution inlet port 14 and is capable of pumping feed solution at a substantially constant rate under pressure into the feed solution chamber 8.
  • An electrially-controlled feed solution discharge throttle valve 24 is connected to the feed-solution outlet port 16 for controlling the liquid pressure of the feed solution flowing through the feed-solution chamber 8.
  • An extractant inlet port 18 and an extractant outlet port 20 permit a liquid extractant to be introduced into and discharged from the extractant chamber 10.
  • An extractant pump 26 is connected to the extractant inlet port 18 and is capable of pumping the liquid extractant through the extractant chamber 10 at a substantially constant rate.
  • An electrically-controlled extractant discharge throttle valve 28 is connected to the extractant outlet port 20 for controlling the liquid pressure of the extractant flowing through the extractant chamber 10.
  • a pressure-difference regulator 30 has a head pressure sensor input 32 in communication with the feed solution chamber 8 for sensing the liquid pressure of the feed solution in the chamber.
  • a base pressure sensor input 34 communicates with the extractant chamber 10 for sensing the fluid pressure of the extractant in the chamber.
  • a throttle valve control-signal output 36 of the pressure-difference regulator 30 is connected to the feed-solution discharge throttle valve 24.
  • the pressure-difference regulator 30 generates a throttle valve control signal at the control signal output 36 which varies in response to changes in the difference between the pressure sensed at the head pressure sensor input 32 and the pressure sensed at the base pressure sensor input 34.
  • the feed solution is pumped by the feed solution pump through the feed-solution chamber 8 at a substantially constant rate.
  • An extractant is pumped by the extractant pump 26 through the extractant chamber 10 at a substantially constant rate.
  • the pressure difference regulator 30 senses the liquid pressure in the feed solution chamber 8 and in the extractant chamber 10 and generates a throttle valve control signal to control the pressure drop across the feed-solution discharge throttle valve 24 so that the difference between the liquid pressure in the feed-solution chamber 8 and the liquid pressure in the extractant chamber 10 is within a predetermined range which is effective substantially to immobilize the interface between the feed solution and the liquid extractant at the membrane 4. Solute from the feed solution is transferred through the pores of the membrane 4 to the extractant.
  • a membrane solute-transfer unit 40 has a three-chamber extraction cell 42.
  • the extraction cell 42 has a housing 44 and a first and a second porous membrane 46 and 48 located within the interior of the housing 44.
  • the first and the second porous membranes 46 and 48 are sealed to the housing 44 and divide the housing into three chambers: a feed solution chamber 50, an intermediate-extractant chamber 52, and a back-extractant chamber 54.
  • the intermediate-extractant chamber 52 is located between the feed-solution chamber 50 and the back-extractant chamber 54.
  • Pores in the first porous membrane 46 provide communication between the feed-solution chamber 50 and the intermediate-extractant chamber 52; pores in the second porous membrane 48 provide communication between the back-extractant chamber 54 and the intermediate-extractant chamber 52.
  • the extraction cell housing 44 has a feed-solution inlet port 56 and a feed-solution outlet port 58 for respectively introducing a feed solution into and discharging the feed solution from the feed solution chamber 50.
  • a feed-solution input pump 60 is connected to the feed solution inlet port 56 and an electrically-controlled feed-solution throttle valve 62 is connected to the feed solution discharge port 58.
  • the extraction cell housing 44 has an intermediate-extractant inlet port 64 to which an intermediate-extractant inlet valve 66 is connected for introducing an intermediate extractant into the intermediate extractant chamber 52.
  • the extractant cell housing 44 also includes an intermediate extractant outlet port 68 to which an intermediate-extractant outlet valve 70 is connected for discharging the intermediate extractant from the intermediate extractant chamber 52.
  • the extractant cell housing 44 also has a back-extractant inlet port 72 to which a back-extractant inlet pump 74 is connected and a back extractant outlet port 76 to which an electrically-controlled back-extractant discharge throttle valve 78 is connected.
  • a first reinforcing screen 80 is located in the extractant cell housing 44 adjacent to the first porous membrane 46 facing the intermediate extractant chamber 52.
  • a second reinforcing screen 82 is located in the extractant-cell housing 44 adjacent to the second porous membrane 48 facing the intermediate-extractant chamber 52.
  • a first pressure difference regulator 84 has a head pressure sensor input 86 which communicates with the feed solution chamber 50 and a base pressure sensor input 88 which communicates with the intermediate extractant chamber 52.
  • a throttle-valve control output 90 of the first pressure difference regulator 84 is connected to a control signal input 63 of the feed-solution discharge throttle valve 62.
  • the first pressure difference regulator 84 is capable of generating a valve control signal at the throttle valve control outlet 90 which varies in accordance with changes in the difference between the liquid pressure at the head pressure sensor input 86 and the liquid pressure at the base pressure sensor input 88.
  • the pressure drop accross the throttle valve 62 and hence the liquid pressure in the feed-solution chamber 50 varies in response to changes in the valve control signal supplied to the control signal input 63 of the valve 62.
  • the first pressure difference regulator 84 can control the difference in pressure between the feed-solution chamber 50 and the intermediate-extractant chamber 52.
  • a second pressure difference regulator 92 has a first pressure sensor input 94 which communicates with the back extractant chamber 54 and a base pressure sensor input 96 which communicates with the intermediate extractant chamber 52.
  • a throttle valve control output 98 is connected to a control input 100 of the back-extractant discharge throttle valve 78.
  • the operation of the second pressure difference regulator 92 is essentially the same as the operation of the first pressure difference regulator 84 with the result that the difference in liquid pressure between the back extractant chamber 54 and the intermediate extractant chamber 52 can be controlled by the second pressure difference regulator 92 to a preset value.
  • the feed solution is pumped by the feed-solution pump 60 at a substantially constant rate through the feed-solution chamber 50 and out through the feed-solution discharge throttle valve 62.
  • the intermediate-extractant chamber 52 is filled with an intermediate extractant liquid which is substantially immiscible with the feed solution.
  • the intermediate extractant in the intermediate extractant chamber 52 preferably remains essentially stagnant, although a trickle flow through the chamber may be maintained if the intermediate extractant degenerates with time.
  • the back-extractant liquid is pumped through the back-extractant chamber 54 at a substantially constant rate by the back-extractant input pump 74 and discharged through the back-extractant discharge throttle valve 78.
  • the intermediate extractant wets the first and the second membranes 46 and 48 preferentially relative to the feed solution and the back extractant. Consequently, the pressure in the feed-solution chamber 50 and the back-extractant chamber 54 is maintained at a value greater than the pressure in the intermediate-extractant chamber 52 in order to oppose the tendency of the intermediate-extractant to flow through the porous membrane.
  • Solute in the feed solution is transferred through the pores of the first porous membrane 46 to the intermediate extractant in the intermediate extractant chamber 52.
  • the solute then diffuses across the intermediate extractant chamber 52 and is transferred through the pores of the second porous membrane 48 to the back-extractant liquid in the back-extractant chamber 54.
  • the solute in the back-extractant chamber 54 is then swept with the back-extractant out the chamber and collected.
  • a solute transfer unit 100 includes an extraction cell 102.
  • the extraction cell 102 includes a generally cylindrical pressure vessel 104 which serves as the housing for the extraction cell.
  • the pressure vessel 104 is made up of a feed-solution input section 106, a solute transfer section 108 and a feed-solution output section 110.
  • a feed-solution input patition 112 is located between the feed-solution input section 106 and the solute-transfer section 108.
  • the volume enclosed by the feed solution input section 106 of the pressure vessel 104 and the input partition 112 defines a feed solution input manifold 122.
  • a feed-solution output partition 114 is located between the solute-transfer section 108 and the feed solution output section 110.
  • the volume enclosed by the feed-solution output section 110 of the pressure vessel 104 and the output partition 114 defines a feed-solution output manifold 124.
  • the volume enclosed by the solute-transfer section 108 of the pressure vessel 104 and the input and output partitions 112 and 114 defines an intermediate extractant chamber 126.
  • the feed-solution input section 106 of the pressure vessel 104 has a feed solution input port 116 which is connected to a feed solution input pump 118 for pumping feed solution into the feed solution input manifold 122.
  • the feed solution output section 110 has a feed-solution output port 120 to which an electrically-controlled feed-solution discharge throttle valve 121 is connected through which feed solution in the feed solution output manifold 124 can be discharged.
  • a plurality of hollow feed-solution solute transfer tubes 128 extend from the feed-solution input manifold 122 to the feed-solution output manifold 124.
  • the feed-solution solute-transfer tubes 128 pass through the input partition 112, extend across the intermediate-extractant chamber 126 and pass through the output bulkhead 114.
  • the solute transfer tubes 128 are embedded in the partitions 112 and 114 by an epoxy adhesive.
  • the hollow solute-transfer tubes 128 are made of porous polypropylene and have a wall thickness of about 18.5 ⁇ m and an inside diameter of about 0.25 mm.
  • the solute transfer section 108 of the pressure vessel 104 has an intermediate extractant inlet port 130 connected to an intermediate-extractant inlet valve 132 for introducing an intermediate-extractant into the intermediate extractant chamber 126.
  • An intermediate extractant outlet port 134 connected to an intermediate outlet valve 136 is provided in the solute-transfer section 108 for discharging intermediate extractant from the intermediate-extractant chamber 126.
  • the solute transfer section 108 of the pressure vessel 104 has a back-extractant inlet port 138 and a final extractant outlet port 140 passing through it.
  • a back-extractant inlet port 138 Connected to the back-extractant inlet port 138 is a back-extracaant input manifold housing 142 the interior of which defines a final extractant input manifold (not shown).
  • a plurality of back-extractant solute-transfer tubes 146 extend from the back-extractant input manifold to the back-extractant output manifold.
  • the back-extractant solute-transfer tubes 146 are made of the same porous polypropylene material as the feed-solution solute-transfer tubes 128.
  • the back-extractant solute-transfer tubes 146 extend through the intermediate-extractant chamber 126 and intermingle with the feed-solution solute transfer tubes 128.
  • the feed-solution solute transfer tubes 128 and the back-extractant solute-transfer tubes 146 are located close to one another to minimize the mean distance the solute must traverse in passing from the one set of tubes to the other.
  • Comingled bundles of the feed-solution solute-transfer tubes 128 and the back-extractant solute-transfer tubes 146 can be prepared as follows. First, about 500 lengths of hollow tubular fiber are cut to substantially the same length to serve as the feed-solution solute-transfer tubes 128. The lengths of fibers are laid side-by-side on a flat surface. By weaving thread crosswise of the hollow tubular fibers in strips at other end, the fibers are bound together to form a flat mat. A similar mat is prepared with about 500 sections of hollow tubular fibers of a length suitable for the back-extractant solute-transfer tubes 146.
  • the back-extractant solute-transfer fibers 146 are longer than the feed-solution solute transfer fibers 128 in the extraction cell 102.
  • the mat of the fibers for the feed-solution solute-transfer fibers 128 is placed on top of the mat for the back-extractant solute-transfer fibers 146, with the fibers of each mat running essentially in parallel and with the shorter mat centered lengthwise on the longer mat.
  • the two mats are then rolled up to form a cylinder with the fibers running generally parallel to the cylinder axis.
  • the cylinder of fibers is then placed in the solute-transfer section 108 of the extraction cell 102.
  • the woven strip of the shorter mat are then unravelled to free the ends of the shorter fibers.
  • the ends of the longer fibers which protrude from either end of the cylinder, are gathered into three or four bundles and brought out through the corresponding back-extractant input or output manifold.
  • the four groups of ends of fibers are then potted separately in epoxy. Especially, the ends are immersed in a layer of liquid epoxy and hardened, which is allowed to cure.
  • the epoxy blocks the openings of most of the hollow fibers.
  • a slice is cut from the epoxy. Depending on the nature of the fibers and the epoxy, the slice may be cut from the epoxy after it has fully cured or when it has only partially cured.
  • the cured epoxy serves as the feed solution input and output partitions 112 and 114.
  • a back-extractant input pump 148 is connected to the back-extractant input fitting 142 for pumping a back-extractant liquid through the back-extractant solute transfer tubes 146.
  • a first pressure difference regulator 150 senses the pressure in the feed-solution input-manifold 122 and the intermediate extractant chamber 126 and controls the feed-solution discharge throttle valve 121 to maintain the difference between the pressure in the feed-solution input manifold and the pressure in the intermediate extractant chamber within a predetermined range.
  • a second pressure difference regulator 152 senses the pressure in the back-extractant input manifold and the intermediate extractant chamber 126 and controls the back-extractant discharge throttle valve 145 to maintain the difference in pressure between the back-extractant input manifold and the intermediate extractant chamber 126 within a predetermined range.
  • the feed-solution input pump 118 pumps a feed solution at a substantially constant rate into the feed-solution input manifold 122, through the feed-solution solute-transfer tubes 128, and into the feed-solution output manifold 124 where it is discharged through the feed solution discharge throttle valve 121.
  • the back-extractant input pump 148 pumps a back-extractant liquid at a substantially constant rate into the back-extractant input manifold, through the back-extractant solute-transfer tubes 146, and into the back-extractant output manifold, from which it is discharged through the back-extractant discharge throttle valve 145.
  • the pressure difference between the feed solution and the intermediate extractant is maintained by the first pressure difference regulator 150 in a range which substantially immobilizes the interface between the feed solution and the intermediate extractant at the porous walls of feed-solution solute-transfer tubes 128.
  • the presssure difference between the back extractant and the intermediate extractant is regulated by the second pressure difference regulator 152 to fall within a range which substantially immobilizes the interface between the back extractant and the intermediate extractant at the porous walls of the back-extractant solute transfer tubes 146.
  • Solute in the feed solution is transferred through the porous walls of the feed solution solute-transfer tubes 128 to the intermediate extractant in the intermediate extractant chamber 126 and thence through the porous walls of the back extractant solute-transfer tubes 146 to the back-extractant flowing in the transfer tubes 146.
  • the back extractant in which the solute is dissolved is collected from the output of the back-extractant discharge throttle valve 145.
  • FIG. 4 illustrates a fourth solute-transfer unit 160 which is generally similar to the third solute-transfer unit 100 described above. For conciseness, only those features of the fourth solute transfer unit 160 which differ from the third solute transfer unit 100 will be discussed below. Corresponding parts in the third and fourth solute-transfer units 100 and 160 are given corresponding reference numerals.
  • the pressure vessel 104' which serves as a housing for the extraction unit 160 includes a back-extractant input section 162 which is located between the feed solution output section 110' and the solute-transfer section 108' of the pressure vessel.
  • a back-extractant output section 164 is located between the feed-solution input section 106' and the solute-transfer section 108'.
  • the feed-solution input partition 112' is located between the feed-solution input section 106' and the back-extractant output section 164.
  • a first intermediate partition 166 is located between the back-extractant output section 164 and the solute transfer section 108'.
  • the volume enclosed by the back-extractant output section 164, the feed-solution input partition 112', and the first intermediate bulkhead 166 defines a extractant output manifold 170.
  • the feed-solution output partition 114' is located between the back-extractant input section 162 and the feed-solution output section 104'.
  • a second intermediate partition 168 is located between the back-extractant input section 162 and the solute-transfer section 108'.
  • the volume enclosed by the back-extractant input section 162, the feed-solution output partition 114 and the second intermediate partition 168 defines a back-extractant input manifold 172.
  • the feed-solution solute-transfer tubes 128' extend from the feed-solution input manifold 122' to the feed-solution output manifold 124'.
  • Each feed-solution solute-transfer tube 128' passes through, in turn: the feed-solution input partition 112', the back-extractant output manifold 170, the first intermediate partition 166, the intermediate-extractant chamber 126', the second intermediate partition 168, the back-extractant manifold 172 and the feed-solution output partition 114'.
  • a non-porous sheath 174 surrounds each fed solution solute transfer tube 128 in the back-extractant input manifold 172 and output manifold 170 to prevent the feed solution and the back-extractant from mixing.
  • solute-transfer unit was used in the Examples set forth below.
  • immobilized-interface extraction cell had a housing consisting of a first and a second generally disk-shaped block of stainless steel.
  • the extraction-cell housing blocks were about 6.4 cm in diameter and about 2.2 cm thick.
  • a generally disk-shaped depression was milled in one face of each block to define a liquid chamber which served as either the extractant chamber or the feed-solution chamber of the extraction cell.
  • the liquid-chamber depressions were approximately 0.25 mm deep and approximately 3.7 cm in diameter.
  • Each extraction-cell housing block had two channels passing through it to serve as liquid inlet and outlet channels.
  • Each channel consisted of a hole which extended radially inward from a side of the block at approximately the midplane of the block and connecting with seven holes extending axially from the midplane to the base of the liquid-chamber depression.
  • the openings of the seven holes for each channel were disposed along a radius of the disk-shaped liquid-chamber depression for about 0.5 cm from the center of the depression to about 1.6 cm from the center.
  • the radius along which the seven openings of one channel were located extended in generally the opposite direction from the radius along which the seven openings of the other channel were located.
  • the use of seven openings into the liquid-chamber depression permitted liquid to be introduced into and withdrawn from the chamber at linear velocities not substantially higher than the linear velocities of the liquid passing through the chamber.
  • Two substantially circular grooves for two O-ring seals were cut in the face of the first extraction cell housing block substantially concentric with one another and encircling the liquid-chamber depression in the face.
  • the radially inner groove was about 4.1 cm in diameter and the radially outer groove was about 5.0 cm in diameter.
  • Porous membranes for the extraction cell were in the form of disks about 4.8 cm in diameter cut from sheets of porous-membrane material.
  • the diameter of the porous membrane disks was greater than the diameter of the inner O-ring seal but less than the diameter of the outer O-ring seal.
  • the porous membrane disks were made of a number of different materials, which are identified in the various examples set forth below.
  • a circular disk of porous stainless-steel screening about 3.7 cm in diameter and about 0.3 mm thick was cut from a sheet of screening available under the trade name "Rigimesh, Grade Z" from Pall Trinity Corporation of Cortland, New York.
  • the disk of screening was just large enough to fit within a depression on the face of a housing block.
  • the disk of screening provided mechanical support for the porous membrane.
  • the extraction cell was assembled by placing O-ring seals in the O-ring seal grooves of the first extraction cell housing block and placing the disk of screening in the liquid-chamber depression in the face of the second housing block.
  • the porous membrane disk was placed over the mouth of the depression on the second housing block on top of the disk of screening in substantially coaxial alignment with the depression.
  • the two extraction cell housing blocks were then clamped together in substantially coaxial alignment with the faces of the blocks having liquid-chamber depressions facing one another.
  • the radially inner O-ring seal held the porous membrane disk in place, and the radially outer O-ring seal formed a liquid-tight seal between the two housing blocks.
  • the two housing blocks were oriented azimuthally relative to one another so that an inlet to the liquid chamber of the first housing block was substantially aligned with an outlet of the liquid chamber in the second housing block, and an outlet to the liquid chamber of the first housing block was substantially aligned with an inlet of the liquid chamber in the second housing block. Consequently, liquid flowing from the inlet to the outlet in the two liquid chambers flowed in generally opposing directions to one another.
  • Two stainless-steel pressure vessels served as reservoirs for the feed solution and the extractant, respectively.
  • Each pressure vessel was connected to an inlet port of one of the liquid chambers of the extractant cell via a pressure line.
  • An adjustable throttle valve was connected to the outlet port for each liquid chamber.
  • a source of compressed air was connected to each pressure vessel across a pressure regulating valve for pressurizing the contents of the pressure vessel to a pressure set by the valve. Pressurizing liquid contained in a pressure vessel to a value above ambient atmospheric pressure caused it to flow under pressure through the liquid chamber connected to the pressure vessel and then from the liquid chamber through the throttle valve to be discharged.
  • the throttle valve was adjusted so that the resistance to flow imposed by the valve was substantially greater than the resistance to flow in the liquid path from the pressure vessel to the throttle valve.
  • the disk of screening in the liquid-chamber depression in the face of the second housing block supported the porous membrane clamped between the two housing blocks against a pressure difference directed from the liquid chamber in the first housing block to the fluid chamber in the second housing block.
  • the screening supported the porous membrane if the pressure in the fluid chamber adjacent to the side of the porous membrane against which the screening was located was less than the pressure on the opposite side of the membrane. Consequently, the liquid which preferentially wet the porous membrane was caused to flow through the liquid chamber which contained the screening.
  • a feed solution of acetic acid in water was prepared from reagent grade glacial acetic acid and distilled water.
  • concentration of acetic acid in the feed solution was found to be about 5.6 ⁇ 10 -4 gmol/ml by titrating an aliquot of the solution with a standard NaOH solution.
  • a disk of porous polypropylene film 4.8 cm in diameter was cut from a sheet of the film.
  • the film was approximately 25 ⁇ m thick and had an effective pore diameter of about 20 nm.
  • the porosity of the film was about 0.38.
  • the film is available under the trade name "Celgard 2400" from Celanese Corporation of Summit, N.J.
  • the disk of porous polypropylene was mounted between the two extraction-cell housing blocks as described above.
  • the pressure vessel connected to the second extraction-cell housing block which contained the disk of screening was charged with pure xylene of ACS grade.
  • the pressure vessel connected to the first housing block was charged with the aqueous acetic acid feed solution.
  • the first pressure vessel was then pressurized to a pressurized just slightly above ambient atmospheric pressure.
  • the throttle valve connected to the outlet of the second housing block was adjusted so that the volume flow rate of xylene through the extraction cell was about 20 cm 3 /min.
  • the second pressure vessel was then charged to a pressure of about 280 kPa above ambient atmospheric pressure.
  • the throttle valve connected to the outlet of the first extraction-cell housing block was adjusted so that the volume flow rate of the aqueous acetic acid feed solution through the extraction cell was about 20 cm 3 /min.
  • Both the aqueous feed solution and the xylene were about 25° C. upon passing through the extraction cell.
  • the aqueous solution discharged from the extraction cell was observed to contain droplets of a xylene phase. However, after several minutes a steady state was reached in which no organic liquid was observed in the aqueous solution discharged from the extraction cell and no aqueous liquid was observed in the xylene phase discharged from the cell.
  • the xylene phase would be expected to contain about 6.6 ⁇ 10 -6 gmol/ml of acetic acid at equilibrium.
  • This equilibrium concentration of acetic acid in xylene was calculated using a distribution coefficient of about 0.012 measured for acetic acid in water and xylene at about 25° C. over a concentration range of acetic acid in xylene which includes the concentration calculated here.
  • the quantity of acetic acid transferred across a unit area of the porous membrane from the aqueous feed solution to the xylene solution per unit time can be measured by collecting the xylene solution discharged from the cell for a given length of time, analyzing the solution collected for total acetic acid content, and dividing the quantity of acetic acid so found by the collection time and by the area of the porous membrane accessable to the feed solution and the xylene.
  • the resulting value for the rate of solute transfer, denoted W has the units gmol acetic acid/cm 2 sec.
  • the rate of solute transfer W can be related to a transfer coefficient K o , which characterizes the porous membrane of the extraction cell. Specifically, the transfer coefficient K o is defined by the equation
  • W is the rate of solute transfer defined above.
  • A is the area of the porous membrane contacted by the feed solution and extractant in the extraction cell.
  • the area A has a value of 13.37 cm 2 .
  • M is the equilibrium distribution coefficient of acetic acid in water and xylene at the concentration of acetic acid in water discharged from the extraction cell and at the temperature of the extraction.
  • C fs is the concentration of acetic acid in the aqueous feed solution at the inlet to the extraction cell.
  • C e is the concentration of the acetic acid in the xylene discharged from the extraction cell.
  • the transfer coefficient K o was found to be about 17.3 ⁇ 10 -4 cm/sec
  • Example 1 The procedure of Example 1 was repeated with the following differences.
  • the porous membrane was a porous polypropylene film having an effective pore diameter of about 40 nm, a thickness of about 25 ⁇ m, and a porosity of about 0.45.
  • the porous polypropylene film is available under the trade name "Celgard 2500” from Calanese Corporation of Summit, N.J.
  • the feed solution was a solution of acetic acid in water with an acetic acid concentration of 4.2 ⁇ 10 -4 gmol/ml.
  • the extractant was xylene.
  • the pressure vessel charged with xylene was pressurized to a pressure above ambient atmospheric pressure just great enough to cause a flow rate of about 32 ml/min of xylene through the extraction cell.
  • the pressure and flow rate of the aqueous feed solution were substantially the same as Example 1.
  • the concentration of acetic acid in the xylene discharged from the extraction cell after a steady state was reached was found to be about 2.54 ⁇ 10 -7 gmol/ml.
  • the solute transfer coefficient K o for the membrane was about 19.7 ⁇ 10 -4 cm/sec.
  • Example 1 The procedure of Example 1 was repeated with the exceptions noted below.
  • porous membrane of porous polytetrafluoroethylene(PTFE) was used.
  • the porous PTFE had an effective pore diameter of about 20 nm, a thickness of about 50 ⁇ m, a porosity of about 0.50, and a minimum pressure for water entry of about 2.4 MPa.
  • the porous PFTE film was available under the trade name "Goretex" from W. L. Gore and Associates of Elton, Md.
  • the feed solution was solution of acetic acid in water having an acetic acid concentration of about 4.2 ⁇ 10 -4 gmol/ml.
  • the extractant was xylene.
  • the flow rate of xylene through the extraction cell was about 50 ml/min and the pressure of the xylene was only slightly above ambient atmospheric pressure.
  • the flow rate of the aqueous feed solution was about 22 ml/min and the pressure was about 69 kPa above ambient atmospheric pressure.
  • the concentration of acetic acid in the xylene discharged from the extraction cell after a steady stake was reached was found to be about 1.2 ⁇ 10 -7 gmol/ml.
  • the solute transfer coefficient K o was about 14.9 ⁇ 10 -4 cm/sec.
  • Example 1 The procedure of Example 1 was repeated with the following exceptions.
  • the porous membrane was porous PTFE having an effective pore diameter of about 200 nm, a thickness of about 63 ⁇ m, a porosity of about 0.78 and a minimum pressure for water entry of about 280 kPa.
  • the porous film had a backing of nonwoven polyester fabric.
  • the film was available under the trade name "Goretex" from W. L. Gore and Associates of Elton, Md.
  • the feed solution used was acetic aced in water having an acetic acid concentration of about 4.2 ⁇ 10 -4 gmol/ml.
  • the extractant was pure xylene.
  • the volume flow rate of the xylene through the extraction all was about 28 ml/min
  • the pressure of the xylene was only slightly greater than ambient atmospheric pressure.
  • the volume flow rate of the aqueous feed solution through the extraction cell was about 20 ml/min.
  • the pressure on the feed solution was about 110 kPa above ambient atmospheric pressure.
  • the concentration of acetic acid in the xylene solution discharged from the extraction cell after a steady state was achieved was found to be about 4.12 ⁇ 10 -7 gmol/ml.
  • the solute transfer coefficient K o was found to be about 28 ⁇ 10 -4 cm/sec.
  • Example 1 The procedure of Example 1 was repeated with the following exceptions.
  • a hydrophilic porous membrane of porous cellulose acetate was used.
  • the porous membrane had an effective pore diameter of about 200 nm and a thickness of about 130 ⁇ m.
  • the porous membrane was available under the trade name "Milipore EG" from Milipore Corporation at Bedford, Mass.
  • a feed solution of acetic acid in water with an acetic acid concentration of about 4 ⁇ 10 -4 gmol/ml was used.
  • the extractant was pure xylene.
  • the extractant had a volume flow rate of about 60 ml/min and a pressure of about 55 kPa above ambient atmospheric pressure.
  • the feed solution had a volume flow rate of about 30 ml/min and a pressure of only slightly above ambient atmospheric pressure.
  • the feed solution was directed through the fluid-chamber depression of the second extraction cell housing block, which contained the disk of screening for support.
  • the aqueous feed solution was introduced into the extraction cell before the xylene in order to allow the feed solution to wet the hydrophilic membrane.
  • the concentration of the acetic acid in the xylene solution discharged from the extraction cell after a steady state was achieved was found to be about 1.6 ⁇ 10 -7 gmol/ml
  • the solute transfer coefficient K o was found to be about 24 ⁇ 10 -4 cm/sec.
  • the porous membrane of example 1 and the feed solution of example 2 were used.
  • the extractant was methylisobutylketone (MIBK).
  • the volume flow rate of the MIBK through the extraction cell was about 22 ml/min.
  • the pressure of the MIBK extractant was only slightly above ambient atmospheric pressure.
  • the volume flow rate of the feed solution was about 33 ml/min and the pressure of the feed solution was about 140 kPa above ambient atmospheric pressure.
  • the concentration of acetic acid in the MIBK solution discharged from the extraction cell after a steady state was achieved was found to be about 3.9 ⁇ 10 -6 gmol/ml.
  • the solute transfer coefficient K o was found to be about 5 ⁇ 10 -4 cm/sec.
  • the screens 80 and 82 in the extraction cell 42 of FIG. 2 can be placed on the opposite side of the membranes if the feed solution and the back extractant preferentially wet the membranes 46 and 48. It is intended to encompass all other embodiments, alternatives and modifications consistent with the present invention.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Urology & Nephrology (AREA)
  • Engineering & Computer Science (AREA)
  • Water Supply & Treatment (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)
  • Extraction Or Liquid Replacement (AREA)

Abstract

An immobilized-interface solute-transfer unit for transferring solute from a feed solution to an extractant liquid comprises a fluid-tight housing and a porous membrane which divides the housing into a feed solution chamber and an extractant chamber. The housing has feed solution inlet and outlet ports which communicate with the feed solution chamber, and extractant inlet an outlet ports which communicate with the extractant chamber. The solute-transfer unit also includes a pressure difference controller for maintaining a difference between a liquid pressure of a feed solution in the feed solution chamber and a liquid pressure of an extractant in the extractant chamber substantially within a predetermined pressure range so that an interface between the feed solution and the extractant is substantially immobilized at the membrane. The solute-transfer unit is particularly adapted for transferring a solute from a feed solution to an extractant, which feed solution and extractant are immiscible with one another when in direct contact.

Description

TECHNICAL FIELD
The present invention relates to a process for transferring solute from a liquid feed solution to a liquid extractant which is substantially immiscible with the feed solution.
BACKGROUND ART
Liquid-liquid extractions are often used in chemical processes to transfer a solute dissolved in a first liquid to a second liquid which is essentially immiscible with the first liquid. The solution of the solute in the first liquid is generally termed a feed solution and the second liquid is generally termed an extractant. The undissolved solute can be a solid, a liquid, or a gas. When the feed solution is brought into contact with the liquid extractant, the solute tends to distribute itself between the two liquids in accordance with the relative solubility of the solute in the two liquids. Since the feed solution and the liquid extractant are essentially immiscible, they form two distinct thermodynamic phases when in contact with one another. These two phases can be physically separated from one another, which effects a separation of a fraction of the solute from the feed solution.
In order to promote a rapid distribution of the solute between a feed solution and an extractant in conventional liquid-liquid extraction processes, the feed solution and the extractant are typically mixed together intimately. However, such intimate mixing frequently gives rise to troublesome problems. For example, the mixing generally involves forming a dispersion of one of (the liquids in the other. Frequently, the resulting dispersion is relatively stable, so that it takes a long time for the dispersed liquid to coalesce. As a result, the throughput of the solute-transfer process is undesirably low or the inventory of feed solution and extractant tied up in the process is undesirably high.
U.S. Pat. No. 3,956,112 to Lee et al. refers to an extraction process in which a porous membrane serves as a partition between two immiscible solvents. Solutes from one solvent are transferred to the other solvent via direct solvent-solvent contact by way of the porous membrane. In practice, however, conventional extraction processes in which immiscible solvents are separated by a porous membrane generally do not prevent one solvent from forming a dispersion in the other. Typically one or the other solvent seeps through the porous membrane and becomes dispersed in the solvent on the other side of the membrane. As a result, conventional extraction processes involving immiscible solvents separated by a porous membrane generally must provide a settling tank and a solvent return mechanism to coalesce the dispersion formed by the seepage of one of the solvents through the membrane and to return the solvent thus recovered to its source.
DISCLOSURE OF THE INVENTION
I have invented a process for transferring solute from a liquid feed solution to a liquid extractant and an apparatus for carrying out liquid-liquid solute-transfer processes which avoids problems of the prior art noted above.
Broadly, the process of the invention involves transferring solute from a feed solution to a liquid extractant through a porous membrane. In an undissolved state, the solute may be a solid, a liquid, or a gas. The feed solution and the extractant, when in direct contact with each other, are essentially immiscible with each other.
The process of the invention includes the step of contacting a first side of the porous membrane with the feed solution containing the solute and contacting a second, opposing side of the membrane with the liquid extractant. The feed solution and the extractant can come into contact through the pores of the membrane. On the surface of the porous membrane, either the feed solution tends to displace the extractant or the extractant tends to displace the feed solution. The fluid which tends to displace the other defines a membrane-wetting liquid.
The process further includes the step of maintaining an interface-immobilizing pressure difference between the feed solution and the extractant. The interface-immobilizing pressure difference is imposed in a direction and a magnitude which is effective to substantially prevent the membrane-wetting liquid from flowing through the membrane and dispersing in the liquid on the opposite side of the membrane. The interface between the feed solution and the extractant is thereby effectively immobilized at the porous membrane.
The effective diameters of the pores of the porous membrane should be sufficiently large to permit a flow of the membrane-wetting liquid through the pores and sufficiently large to permit the solute to pass through the pores. The membrane should be mechanically strong enough--with suitable reinforcement, if necessary--to withstand the interface-immobilizing pressure difference imposed across the membrane under the intended operating conditions. In certain cases, the membrane material may swell in the presence of the feed solution or the extractant. So long as the swollen membrane remains strong enough to withstand the interface-immobilizing pressure difference, the swelling of the membrane should not be a disadvantage.
The interface-immobilizing pressure difference should be imposed in a direction to oppose the tendency of the membrane-wetting liquid to pass through the membrane. Thus a greater pressure is imposed on the liquid opposite to the membrane-wetting liquid than is imposed on the membrane-wetting liquid in order to oppose the tendency of the membrane-wetting liquid to pass through the membrane.
The range of differences in pressure effective to immobilize the interface between a particular feed solution and extractant at a particular porous membrane depends on a number of factors, including the relative tendency of the feed solution and the extractant to wet the membrane material, the interfacial tension between the feed solution and the extractant, the flow characteristics of each liquid at the surface of the membrane, and the effective diameters of the pores of the membrane. The minimum value of the pressure difference effective to immobilize the interface between the feed solution and the extractant at the porous membrane cannot in general be predicted a priori, largely because the formation of a dispersion depends strongly on the pattern of flow of the liquids at the surface of the membrane. As a practical matter, the average minimum pressure difference opposing the tendency of the membrane-wetting liquid to pass through the membrane should at least be greater than any pressure-difference fluctuations in the opposite direction which, for example, might be expected to be caused by pumping irregularities. In general, the smaller the pores of the membrane and the greater the interfacial tension between the feed solution and the extractant, the greater is the maximum pressure difference which is effective to immobilize the interface. Because of the number of factors involved, it is preferred to establish a range for the interface-immobilizing pressure difference experimentally for a particular porous membrane, feed solution and extractant. A pressure difference range of from about 5 kPa to about 620 kPa has been found to be suitable for certain applications, with the range of from about 140 kPa to about 410 kPa being particularly preferred.
A membrane solute transfer unit for carrying out solute-transfer processes such as the process of the invention includes a porous membrane located within a liquid-tight housing. The porous membrane divides the interior of the housing into two chambers: a feed solution chamber and an extractant chamber. Pores of the membrane provide communication between the two chambers. The housing is provided with inlet and outlet ports which permit feed solution to be introduced and discharged from the feed solution chamber and liquid extractant to be introduced and discharged from the extractant chamber.
The solute-transfer unit of the invention also includes a mechanism for controlling the difference between the liquid pressure of feed solution in the feed solution chamber and the liquid pressure of the extractant in the extractant chamber. The pressure difference is controlled so that it falls within a pressure range effective substantially to immobilize an interface between of the feed solution and the extractant at the porous membrane.
The porous membranes of the present invention may be hydrophilic or hydrophobic. Preferred hydrophilic membranes include porous regenerated cellulose, porous cellulose acetate, porous cellulose acetate-nitrate, porous cellulose triacetate, microporous glass, and porous porcelain. Preferred hydrophobic membranes include porous polyethylene, porous polypropylene, and porous polytetrafluoroethylene (PFTE). The effective diameters of the pores of the membrane preferably lie in the range of from about 1 nm to about 10 μm. The porous membrane should be as thin as is consistent with the need to be strong enough to withstand the interface-immobilizing pressure difference applied across the membrane. Porous membranes from about 25 μm to about 125 μm in thickness are preferred.
For solute-transfer processes carried out on an industrial scale, it is preferred for the porous membrane to be in the form of hollow tubular fibers with porous walls. Bundles of large numbers of such tubular fibers can provide a high value for the ratio of the area of porous membrane through which the solute transfer occurs to the volume of the vessel which contains the feed solution/membrane/extractant system. It is ordinarily preferred for the liquid which preferentially wets the porous wall of the tubular fiber to be located within the lumen of the fiber, since in that case the interface-immobilizing pressure difference would be directed from the outside of the tubular fiber to the inside of the fiber, thereby tending to compress the tubular wall of the fiber. Generally, the walls of tubular fibers are stronger in compression than in tension. Preferably the walls of the tubular fibers are sufficiently thick relative to the diameter of the tube to permit the tube to withstand a compressive interface-immobilizing pressure difference without collapsing. When a liquid is caused to flow through a hollow tubular fiber, a significant pressure drop can occur between the inlet and outlet ends of the fiber. Care should be taken to ensure that an interface-immobilizing pressure difference is maintained across the porous wall of a hollow tubular fiber along the entire length of the fiber.
The present invention permits two or more solute-transfer processes to be carried out conveniently at the same time in a single vessel. For example, a preferred double-transfer solute-transfer unit includes a liquid-tight housing, the interior of which is divided by two porous membranes into a sequence of three side-by-side chambers. A feed solution could be pumped through a first end chamber. An intermediate chamber separated from the first end chamber by a first porous membrane could contain an intermediate extractant liquid substantially immisible with the feed solution. A second end chamber separated from the intermediate chamber by a second porous membrane could have pumped through it a back-extractant liquid which is immisible with the intermediate extractant. The back-extractant liquid could be completely miscible with the feed solution, if desired. Solute in the feed solution in the first chamber could be transferred to the intermediate extractant in the intermediate chamber through the first porous membrane. The solute could then diffuse through the intermediate extractant to the second porous membrane and then be transferred to the back extractant through the second membrane. The intermediate chamber preferably is as narrow as practical to minimize the diffusion path length and to minimize the inventory of intermediate extractant and solute held up in the intermediate chamber. A first interface-immobilizing pressure difference should be maintained across the first membrane to oppose the tendency of the feed solution or the intermediate extractant, as the case may be, to pass through the membrane. A second interface-immobilizing pressure difference should be maintained across the second membrane to oppose the tendency of the intermediate extractant or the back extractant, as the case may be, to pass through the membrane.
Alternatively, a feed solution could be pumped through the intermediate chamber of the preferred double-transfer solute-transfer unit discussed in the preceding paragraph. First and second extractant liquids, each immiscible with the feed solution, could be pumped through the first and second end chambers. An interface-immobilizing pressure difference should then be maintained across each of the first and the second porous membrane to oppose the tendency of one or the other of the feed solution or extractant liquid to pass through the membrane. By using two different extractant liquids, two different solutes could be extracted from a single feed solution at the same time.
For industrial scale solute-transfer processes involving two or more simultaneous solute transfers, it is preferred to employ a plurality of bundles of hollow tubular fibers with porous walls. For example, in the case of a process involving a solute transferred from a feed solution to a back extractant by way of an intermediate extractant which is substantially immiscible with both the feed solution and the back extractant, a preferred double-transfer extraction cell includes two bundles of hollow tubular fibers with porous walls passing through the interior of a liquid-tight housing. The feed solution is pumped through the first bundle of tubular fibers and the back extractant is pumped through the second bundle of tubular fibers. The intermediate extractant fills the interior of the housing, exterior of the tubular fibers. The fibers of the two bundles are preferably commingled and located close to one another to reduce the diffusion path length from the fibers containing the feed solution to the fibers containing the back extractant.
The mechanism for maintaining an interface-immobilizing pressure difference across a porous membrane in the process of the invention may be a closed-loop feed back-type pressure regulating system, if desired. A preferred closed-loop pressure regulating system would sense the liquid pressure on both sides of the porous membrane and control the fluid pressure on one side or the other to maintain the difference between the pressures to within a preset range. Alternatively, the mechanism for maintaining an interface-immobilizing pressure difference across the porous membrane could be an open loop pressure regulating system. In a preferred open-loop pressure regulating system, the liquid pressure on a first side of the membrane is maintained at a first preset value and a liquid pressure on the opposite side of the membrane is maintained at a second preset value essentially independently of the pressure on the first side. The two preset values are chosen so that the difference between the pressure on the two sides falls within a desired interface-immobilizing pressure range.
It is expected that the solute-transfer process of the invention will have wide utility in the chemical and pharmaceutical industries. In fermentation processes, for example, fermentation products can be continuously withdrawn from an aqueous fermentation broth as the fermentation proceeds by transfer to an organic solvent which is immiscible with water. Ethyl alcohol could be extracted from such a broth by a solvent such as dibutyl phthalate or tributyl phosphate separated from the broth by a membrane of porous polypropylene. Cellular debris and other particulate matter in the broth would be prevented from contaminating the solvent stream by the porous membrane. Antibiotics or other fermentation products could be extracted from the broth in an analogous manner with appropriate extractant liquids. Oxygen could be introduced into and carbon dioxide withdrawn from the fermentation broth using a gas-permeable membrane at the same time as fermentation products were being extracted using the process of the invention.
The process of the invention could also be used to separate phenol from waste water using MIBK or diisopropylether as an extractant. If the waste water contained hydrogen sulfide or ammonia in addition to phenol, the MIBK or diisopropylether extractant could be used to extract the phenol and the hydrogen sulfide or ammonia could be removed simultaneously using a gas-permeable membrane. Aromatics could be extracted from petroleum distillates using sulfolane or propylene carbonate as an extractant. Other applications of the solute-transfer process of the invention will occur to persons skilled in the art.
BRIEF DESCRIPTIONS OF THE DRAWINGS
Preferred membrane solute-transfer units of the invention are described below with reference to the following figures:
FIG. 1 is a schematic diagram of a first preferred membrane solute-transfer unit.
FIG. 2 is a schematic diagram of a second preferred membrane solute-transfer unit which employs an intermediate extractant.
FIG. 3 is a schematic diagram of a third preferred membrane solute-transfer unit which employs porous membranes in the form of hollow tubes.
FIG. 4 is a schematic diagram of a fourth preferred membrane solute-transfer unit which employs porous membranes in the form of hollow tubes.
BEST MODE FOR CARRYING OUT THE INVENTION
Turning now to FIG. 1, a membrane solute-transfer unit 2 includes an extraction cell 3 which has a porous membrane 4 located within a housing 6. The membrane 4 is sealed to the walls of the housing 6 and divides the interior of the housing into a feed solution chamber 8 and a liquid extractant chamber 10. Pores passing through the membrane 4 provide communication between the feed solution chamber 8 and the extractant chamber 10. A reinforcing screen 12 is adjacent to the porous membrane 4 on the side of the membrane facing the extractant chamber 10. The screen 12 provides mechanical support for the membrane 4.
A feed-solution inlet port 14 and a feed-solution outlet port 16 permits a feed solution to be introduced into and discharged from the feed solution chamber 8. A feed-solution pump 22 is connected to the feed-solution inlet port 14 and is capable of pumping feed solution at a substantially constant rate under pressure into the feed solution chamber 8. An electrially-controlled feed solution discharge throttle valve 24 is connected to the feed-solution outlet port 16 for controlling the liquid pressure of the feed solution flowing through the feed-solution chamber 8.
An extractant inlet port 18 and an extractant outlet port 20 permit a liquid extractant to be introduced into and discharged from the extractant chamber 10. An extractant pump 26 is connected to the extractant inlet port 18 and is capable of pumping the liquid extractant through the extractant chamber 10 at a substantially constant rate. An electrically-controlled extractant discharge throttle valve 28 is connected to the extractant outlet port 20 for controlling the liquid pressure of the extractant flowing through the extractant chamber 10.
A pressure-difference regulator 30 has a head pressure sensor input 32 in communication with the feed solution chamber 8 for sensing the liquid pressure of the feed solution in the chamber. A base pressure sensor input 34 communicates with the extractant chamber 10 for sensing the fluid pressure of the extractant in the chamber. A throttle valve control-signal output 36 of the pressure-difference regulator 30 is connected to the feed-solution discharge throttle valve 24. The pressure-difference regulator 30 generates a throttle valve control signal at the control signal output 36 which varies in response to changes in the difference between the pressure sensed at the head pressure sensor input 32 and the pressure sensed at the base pressure sensor input 34.
In operation, the feed solution is pumped by the feed solution pump through the feed-solution chamber 8 at a substantially constant rate. An extractant is pumped by the extractant pump 26 through the extractant chamber 10 at a substantially constant rate. The pressure difference regulator 30 senses the liquid pressure in the feed solution chamber 8 and in the extractant chamber 10 and generates a throttle valve control signal to control the pressure drop across the feed-solution discharge throttle valve 24 so that the difference between the liquid pressure in the feed-solution chamber 8 and the liquid pressure in the extractant chamber 10 is within a predetermined range which is effective substantially to immobilize the interface between the feed solution and the liquid extractant at the membrane 4. Solute from the feed solution is transferred through the pores of the membrane 4 to the extractant.
Turning now to FIG. 2, a membrane solute-transfer unit 40 has a three-chamber extraction cell 42. The extraction cell 42 has a housing 44 and a first and a second porous membrane 46 and 48 located within the interior of the housing 44. The first and the second porous membranes 46 and 48 are sealed to the housing 44 and divide the housing into three chambers: a feed solution chamber 50, an intermediate-extractant chamber 52, and a back-extractant chamber 54. The intermediate-extractant chamber 52 is located between the feed-solution chamber 50 and the back-extractant chamber 54. Pores in the first porous membrane 46 provide communication between the feed-solution chamber 50 and the intermediate-extractant chamber 52; pores in the second porous membrane 48 provide communication between the back-extractant chamber 54 and the intermediate-extractant chamber 52.
The extraction cell housing 44 has a feed-solution inlet port 56 and a feed-solution outlet port 58 for respectively introducing a feed solution into and discharging the feed solution from the feed solution chamber 50. A feed-solution input pump 60 is connected to the feed solution inlet port 56 and an electrically-controlled feed-solution throttle valve 62 is connected to the feed solution discharge port 58. The extraction cell housing 44 has an intermediate-extractant inlet port 64 to which an intermediate-extractant inlet valve 66 is connected for introducing an intermediate extractant into the intermediate extractant chamber 52. The extractant cell housing 44 also includes an intermediate extractant outlet port 68 to which an intermediate-extractant outlet valve 70 is connected for discharging the intermediate extractant from the intermediate extractant chamber 52. The extractant cell housing 44 also has a back-extractant inlet port 72 to which a back-extractant inlet pump 74 is connected and a back extractant outlet port 76 to which an electrically-controlled back-extractant discharge throttle valve 78 is connected.
A first reinforcing screen 80 is located in the extractant cell housing 44 adjacent to the first porous membrane 46 facing the intermediate extractant chamber 52. A second reinforcing screen 82 is located in the extractant-cell housing 44 adjacent to the second porous membrane 48 facing the intermediate-extractant chamber 52.
A first pressure difference regulator 84 has a head pressure sensor input 86 which communicates with the feed solution chamber 50 and a base pressure sensor input 88 which communicates with the intermediate extractant chamber 52. A throttle-valve control output 90 of the first pressure difference regulator 84 is connected to a control signal input 63 of the feed-solution discharge throttle valve 62. The first pressure difference regulator 84 is capable of generating a valve control signal at the throttle valve control outlet 90 which varies in accordance with changes in the difference between the liquid pressure at the head pressure sensor input 86 and the liquid pressure at the base pressure sensor input 88. The pressure drop accross the throttle valve 62 and hence the liquid pressure in the feed-solution chamber 50 varies in response to changes in the valve control signal supplied to the control signal input 63 of the valve 62. As a result, the first pressure difference regulator 84 can control the difference in pressure between the feed-solution chamber 50 and the intermediate-extractant chamber 52.
A second pressure difference regulator 92 has a first pressure sensor input 94 which communicates with the back extractant chamber 54 and a base pressure sensor input 96 which communicates with the intermediate extractant chamber 52. A throttle valve control output 98 is connected to a control input 100 of the back-extractant discharge throttle valve 78. The operation of the second pressure difference regulator 92 is essentially the same as the operation of the first pressure difference regulator 84 with the result that the difference in liquid pressure between the back extractant chamber 54 and the intermediate extractant chamber 52 can be controlled by the second pressure difference regulator 92 to a preset value.
In operation, the feed solution is pumped by the feed-solution pump 60 at a substantially constant rate through the feed-solution chamber 50 and out through the feed-solution discharge throttle valve 62. The intermediate-extractant chamber 52 is filled with an intermediate extractant liquid which is substantially immiscible with the feed solution. The intermediate extractant in the intermediate extractant chamber 52 preferably remains essentially stagnant, although a trickle flow through the chamber may be maintained if the intermediate extractant degenerates with time. The back-extractant liquid is pumped through the back-extractant chamber 54 at a substantially constant rate by the back-extractant input pump 74 and discharged through the back-extractant discharge throttle valve 78.
In the three-chamber extractant cell of FIG. 2, the intermediate extractant wets the first and the second membranes 46 and 48 preferentially relative to the feed solution and the back extractant. Consequently, the pressure in the feed-solution chamber 50 and the back-extractant chamber 54 is maintained at a value greater than the pressure in the intermediate-extractant chamber 52 in order to oppose the tendency of the intermediate-extractant to flow through the porous membrane.
Solute in the feed solution is transferred through the pores of the first porous membrane 46 to the intermediate extractant in the intermediate extractant chamber 52. The solute then diffuses across the intermediate extractant chamber 52 and is transferred through the pores of the second porous membrane 48 to the back-extractant liquid in the back-extractant chamber 54. The solute in the back-extractant chamber 54 is then swept with the back-extractant out the chamber and collected.
Turning now to FIG. 3, a solute transfer unit 100 includes an extraction cell 102. The extraction cell 102 includes a generally cylindrical pressure vessel 104 which serves as the housing for the extraction cell. The pressure vessel 104 is made up of a feed-solution input section 106, a solute transfer section 108 and a feed-solution output section 110. A feed-solution input patition 112 is located between the feed-solution input section 106 and the solute-transfer section 108. The volume enclosed by the feed solution input section 106 of the pressure vessel 104 and the input partition 112 defines a feed solution input manifold 122. A feed-solution output partition 114 is located between the solute-transfer section 108 and the feed solution output section 110. The volume enclosed by the feed-solution output section 110 of the pressure vessel 104 and the output partition 114 defines a feed-solution output manifold 124. The volume enclosed by the solute-transfer section 108 of the pressure vessel 104 and the input and output partitions 112 and 114 defines an intermediate extractant chamber 126.
The feed-solution input section 106 of the pressure vessel 104 has a feed solution input port 116 which is connected to a feed solution input pump 118 for pumping feed solution into the feed solution input manifold 122. The feed solution output section 110 has a feed-solution output port 120 to which an electrically-controlled feed-solution discharge throttle valve 121 is connected through which feed solution in the feed solution output manifold 124 can be discharged. A plurality of hollow feed-solution solute transfer tubes 128 extend from the feed-solution input manifold 122 to the feed-solution output manifold 124. The feed-solution solute-transfer tubes 128 pass through the input partition 112, extend across the intermediate-extractant chamber 126 and pass through the output bulkhead 114. The solute transfer tubes 128 are embedded in the partitions 112 and 114 by an epoxy adhesive. The hollow solute-transfer tubes 128 are made of porous polypropylene and have a wall thickness of about 18.5 μm and an inside diameter of about 0.25 mm.
The solute transfer section 108 of the pressure vessel 104 has an intermediate extractant inlet port 130 connected to an intermediate-extractant inlet valve 132 for introducing an intermediate-extractant into the intermediate extractant chamber 126. An intermediate extractant outlet port 134 connected to an intermediate outlet valve 136 is provided in the solute-transfer section 108 for discharging intermediate extractant from the intermediate-extractant chamber 126.
The solute transfer section 108 of the pressure vessel 104 has a back-extractant inlet port 138 and a final extractant outlet port 140 passing through it. Connected to the back-extractant inlet port 138 is a back-extracaant input manifold housing 142 the interior of which defines a final extractant input manifold (not shown).
A plurality of back-extractant solute-transfer tubes 146 extend from the back-extractant input manifold to the back-extractant output manifold. The back-extractant solute-transfer tubes 146 are made of the same porous polypropylene material as the feed-solution solute-transfer tubes 128. The back-extractant solute-transfer tubes 146 extend through the intermediate-extractant chamber 126 and intermingle with the feed-solution solute transfer tubes 128. The feed-solution solute transfer tubes 128 and the back-extractant solute-transfer tubes 146 are located close to one another to minimize the mean distance the solute must traverse in passing from the one set of tubes to the other. Comingled bundles of the feed-solution solute-transfer tubes 128 and the back-extractant solute-transfer tubes 146 can be prepared as follows. First, about 500 lengths of hollow tubular fiber are cut to substantially the same length to serve as the feed-solution solute-transfer tubes 128. The lengths of fibers are laid side-by-side on a flat surface. By weaving thread crosswise of the hollow tubular fibers in strips at other end, the fibers are bound together to form a flat mat. A similar mat is prepared with about 500 sections of hollow tubular fibers of a length suitable for the back-extractant solute-transfer tubes 146. The back-extractant solute-transfer fibers 146 are longer than the feed-solution solute transfer fibers 128 in the extraction cell 102. The mat of the fibers for the feed-solution solute-transfer fibers 128 is placed on top of the mat for the back-extractant solute-transfer fibers 146, with the fibers of each mat running essentially in parallel and with the shorter mat centered lengthwise on the longer mat. The two mats are then rolled up to form a cylinder with the fibers running generally parallel to the cylinder axis. The cylinder of fibers is then placed in the solute-transfer section 108 of the extraction cell 102. The woven strip of the shorter mat are then unravelled to free the ends of the shorter fibers. The ends of the longer fibers, which protrude from either end of the cylinder, are gathered into three or four bundles and brought out through the corresponding back-extractant input or output manifold. The four groups of ends of fibers are then potted separately in epoxy. Especially, the ends are immersed in a layer of liquid epoxy and hardened, which is allowed to cure. The epoxy blocks the openings of most of the hollow fibers. In order to reopen the openings in the fibers, a slice is cut from the epoxy. Depending on the nature of the fibers and the epoxy, the slice may be cut from the epoxy after it has fully cured or when it has only partially cured. The cured epoxy serves as the feed solution input and output partitions 112 and 114.
A back-extractant input pump 148 is connected to the back-extractant input fitting 142 for pumping a back-extractant liquid through the back-extractant solute transfer tubes 146.
A first pressure difference regulator 150 senses the pressure in the feed-solution input-manifold 122 and the intermediate extractant chamber 126 and controls the feed-solution discharge throttle valve 121 to maintain the difference between the pressure in the feed-solution input manifold and the pressure in the intermediate extractant chamber within a predetermined range. Similarly, a second pressure difference regulator 152 senses the pressure in the back-extractant input manifold and the intermediate extractant chamber 126 and controls the back-extractant discharge throttle valve 145 to maintain the difference in pressure between the back-extractant input manifold and the intermediate extractant chamber 126 within a predetermined range.
In operation, the feed-solution input pump 118 pumps a feed solution at a substantially constant rate into the feed-solution input manifold 122, through the feed-solution solute-transfer tubes 128, and into the feed-solution output manifold 124 where it is discharged through the feed solution discharge throttle valve 121. The back-extractant input pump 148 pumps a back-extractant liquid at a substantially constant rate into the back-extractant input manifold, through the back-extractant solute-transfer tubes 146, and into the back-extractant output manifold, from which it is discharged through the back-extractant discharge throttle valve 145.
The pressure difference between the feed solution and the intermediate extractant is maintained by the first pressure difference regulator 150 in a range which substantially immobilizes the interface between the feed solution and the intermediate extractant at the porous walls of feed-solution solute-transfer tubes 128. Similarly, the presssure difference between the back extractant and the intermediate extractant is regulated by the second pressure difference regulator 152 to fall within a range which substantially immobilizes the interface between the back extractant and the intermediate extractant at the porous walls of the back-extractant solute transfer tubes 146.
Solute in the feed solution is transferred through the porous walls of the feed solution solute-transfer tubes 128 to the intermediate extractant in the intermediate extractant chamber 126 and thence through the porous walls of the back extractant solute-transfer tubes 146 to the back-extractant flowing in the transfer tubes 146. The back extractant in which the solute is dissolved is collected from the output of the back-extractant discharge throttle valve 145.
FIG. 4 illustrates a fourth solute-transfer unit 160 which is generally similar to the third solute-transfer unit 100 described above. For conciseness, only those features of the fourth solute transfer unit 160 which differ from the third solute transfer unit 100 will be discussed below. Corresponding parts in the third and fourth solute- transfer units 100 and 160 are given corresponding reference numerals.
The pressure vessel 104' which serves as a housing for the extraction unit 160 includes a back-extractant input section 162 which is located between the feed solution output section 110' and the solute-transfer section 108' of the pressure vessel. A back-extractant output section 164 is located between the feed-solution input section 106' and the solute-transfer section 108'. The feed-solution input partition 112' is located between the feed-solution input section 106' and the back-extractant output section 164. A first intermediate partition 166 is located between the back-extractant output section 164 and the solute transfer section 108'. The volume enclosed by the back-extractant output section 164, the feed-solution input partition 112', and the first intermediate bulkhead 166 defines a extractant output manifold 170.
The feed-solution output partition 114' is located between the back-extractant input section 162 and the feed-solution output section 104'. A second intermediate partition 168 is located between the back-extractant input section 162 and the solute-transfer section 108'. The volume enclosed by the back-extractant input section 162, the feed-solution output partition 114 and the second intermediate partition 168 defines a back-extractant input manifold 172.
The feed-solution solute-transfer tubes 128' extend from the feed-solution input manifold 122' to the feed-solution output manifold 124'. Each feed-solution solute-transfer tube 128' passes through, in turn: the feed-solution input partition 112', the back-extractant output manifold 170, the first intermediate partition 166, the intermediate-extractant chamber 126', the second intermediate partition 168, the back-extractant manifold 172 and the feed-solution output partition 114'. A non-porous sheath 174 surrounds each fed solution solute transfer tube 128 in the back-extractant input manifold 172 and output manifold 170 to prevent the feed solution and the back-extractant from mixing.
EXAMPLES
The following solute-transfer unit was used in the Examples set forth below.
As immobilized-interface extraction cell had a housing consisting of a first and a second generally disk-shaped block of stainless steel. The extraction-cell housing blocks were about 6.4 cm in diameter and about 2.2 cm thick. A generally disk-shaped depression was milled in one face of each block to define a liquid chamber which served as either the extractant chamber or the feed-solution chamber of the extraction cell. The liquid-chamber depressions were approximately 0.25 mm deep and approximately 3.7 cm in diameter.
Each extraction-cell housing block had two channels passing through it to serve as liquid inlet and outlet channels. Each channel consisted of a hole which extended radially inward from a side of the block at approximately the midplane of the block and connecting with seven holes extending axially from the midplane to the base of the liquid-chamber depression. The openings of the seven holes for each channel were disposed along a radius of the disk-shaped liquid-chamber depression for about 0.5 cm from the center of the depression to about 1.6 cm from the center. The radius along which the seven openings of one channel were located extended in generally the opposite direction from the radius along which the seven openings of the other channel were located. The use of seven openings into the liquid-chamber depression permitted liquid to be introduced into and withdrawn from the chamber at linear velocities not substantially higher than the linear velocities of the liquid passing through the chamber.
Two substantially circular grooves for two O-ring seals were cut in the face of the first extraction cell housing block substantially concentric with one another and encircling the liquid-chamber depression in the face. The radially inner groove was about 4.1 cm in diameter and the radially outer groove was about 5.0 cm in diameter.
Porous membranes for the extraction cell were in the form of disks about 4.8 cm in diameter cut from sheets of porous-membrane material. The diameter of the porous membrane disks was greater than the diameter of the inner O-ring seal but less than the diameter of the outer O-ring seal. The porous membrane disks were made of a number of different materials, which are identified in the various examples set forth below.
A circular disk of porous stainless-steel screening about 3.7 cm in diameter and about 0.3 mm thick was cut from a sheet of screening available under the trade name "Rigimesh, Grade Z" from Pall Trinity Corporation of Cortland, New York. The disk of screening was just large enough to fit within a depression on the face of a housing block. The disk of screening provided mechanical support for the porous membrane.
The extraction cell was assembled by placing O-ring seals in the O-ring seal grooves of the first extraction cell housing block and placing the disk of screening in the liquid-chamber depression in the face of the second housing block. The porous membrane disk was placed over the mouth of the depression on the second housing block on top of the disk of screening in substantially coaxial alignment with the depression. The two extraction cell housing blocks were then clamped together in substantially coaxial alignment with the faces of the blocks having liquid-chamber depressions facing one another. The radially inner O-ring seal held the porous membrane disk in place, and the radially outer O-ring seal formed a liquid-tight seal between the two housing blocks.
The two housing blocks were oriented azimuthally relative to one another so that an inlet to the liquid chamber of the first housing block was substantially aligned with an outlet of the liquid chamber in the second housing block, and an outlet to the liquid chamber of the first housing block was substantially aligned with an inlet of the liquid chamber in the second housing block. Consequently, liquid flowing from the inlet to the outlet in the two liquid chambers flowed in generally opposing directions to one another.
Two stainless-steel pressure vessels served as reservoirs for the feed solution and the extractant, respectively. Each pressure vessel was connected to an inlet port of one of the liquid chambers of the extractant cell via a pressure line. An adjustable throttle valve was connected to the outlet port for each liquid chamber. A source of compressed air was connected to each pressure vessel across a pressure regulating valve for pressurizing the contents of the pressure vessel to a pressure set by the valve. Pressurizing liquid contained in a pressure vessel to a value above ambient atmospheric pressure caused it to flow under pressure through the liquid chamber connected to the pressure vessel and then from the liquid chamber through the throttle valve to be discharged. The throttle valve was adjusted so that the resistance to flow imposed by the valve was substantially greater than the resistance to flow in the liquid path from the pressure vessel to the throttle valve. Consequently, essentially all of the pressure drop between the pressure in the pressure vessel and the ambient atmospheric pressure at the discharge outlet of the throttle valve occurred across the throttle valve. As a result, the pressure in the liquid chamber was substantially the same as the pressure impressed on the liquid in the pressure vessel by the compressed air. Thus, if the pressure in one pressure vessel differed from the pressure in the second pressure vessel by a selected amount, the pressure in the two fluid chambers connected respectively to the two pressure vessels differed by essentially the same amount.
The disk of screening in the liquid-chamber depression in the face of the second housing block supported the porous membrane clamped between the two housing blocks against a pressure difference directed from the liquid chamber in the first housing block to the fluid chamber in the second housing block. In other words, the screening supported the porous membrane if the pressure in the fluid chamber adjacent to the side of the porous membrane against which the screening was located was less than the pressure on the opposite side of the membrane. Consequently, the liquid which preferentially wet the porous membrane was caused to flow through the liquid chamber which contained the screening.
EXAMPLE 1
A feed solution of acetic acid in water was prepared from reagent grade glacial acetic acid and distilled water. The concentration of acetic acid in the feed solution was found to be about 5.6×10-4 gmol/ml by titrating an aliquot of the solution with a standard NaOH solution.
A disk of porous polypropylene film 4.8 cm in diameter was cut from a sheet of the film. The film was approximately 25 μm thick and had an effective pore diameter of about 20 nm. The porosity of the film was about 0.38. The film is available under the trade name "Celgard 2400" from Celanese Corporation of Summit, N.J.
The disk of porous polypropylene was mounted between the two extraction-cell housing blocks as described above. The pressure vessel connected to the second extraction-cell housing block which contained the disk of screening was charged with pure xylene of ACS grade. The pressure vessel connected to the first housing block was charged with the aqueous acetic acid feed solution.
The first pressure vessel was then pressurized to a pressurized just slightly above ambient atmospheric pressure. The throttle valve connected to the outlet of the second housing block was adjusted so that the volume flow rate of xylene through the extraction cell was about 20 cm3 /min.
The second pressure vessel was then charged to a pressure of about 280 kPa above ambient atmospheric pressure. The throttle valve connected to the outlet of the first extraction-cell housing block was adjusted so that the volume flow rate of the aqueous acetic acid feed solution through the extraction cell was about 20 cm3 /min.
Both the aqueous feed solution and the xylene were about 25° C. upon passing through the extraction cell.
Initially the aqueous solution discharged from the extraction cell was observed to contain droplets of a xylene phase. However, after several minutes a steady state was reached in which no organic liquid was observed in the aqueous solution discharged from the extraction cell and no aqueous liquid was observed in the xylene phase discharged from the cell.
An aliquot of the xylene phase discharged from the extraction cell was collected after the steady state was reached and analyzed for acetic acid content by titrating with a standard NaOH solution. The xylene was found to contain 4.66×10-7 gmol/ml acetic acid.
For comparison, if equal volumes of the aqueous acetic acid feed solution and xylene were mixed together and allowed to equilibrate at 25° C., the xylene phase would be expected to contain about 6.6×10-6 gmol/ml of acetic acid at equilibrium. This equilibrium concentration of acetic acid in xylene was calculated using a distribution coefficient of about 0.012 measured for acetic acid in water and xylene at about 25° C. over a concentration range of acetic acid in xylene which includes the concentration calculated here.
After the steady state conditions have been reached in the extraction cell, the quantity of acetic acid transferred across a unit area of the porous membrane from the aqueous feed solution to the xylene solution per unit time can be measured by collecting the xylene solution discharged from the cell for a given length of time, analyzing the solution collected for total acetic acid content, and dividing the quantity of acetic acid so found by the collection time and by the area of the porous membrane accessable to the feed solution and the xylene. The resulting value for the rate of solute transfer, denoted W, has the units gmol acetic acid/cm2 sec. The rate of solute transfer W can be related to a transfer coefficient Ko, which characterizes the porous membrane of the extraction cell. Specifically, the transfer coefficient Ko is defined by the equation
W=K.sub.o A(m C.sub.fs -C.sub.e)
where:
W is the rate of solute transfer defined above.
A is the area of the porous membrane contacted by the feed solution and extractant in the extraction cell. In the present extraction cell, the area A has a value of 13.37 cm2.
M is the equilibrium distribution coefficient of acetic acid in water and xylene at the concentration of acetic acid in water discharged from the extraction cell and at the temperature of the extraction.
Cfs is the concentration of acetic acid in the aqueous feed solution at the inlet to the extraction cell.
Ce is the concentration of the acetic acid in the xylene discharged from the extraction cell. In the present example, the transfer coefficient Ko was found to be about 17.3×10-4 cm/sec
EXAMPLE 2
The procedure of Example 1 was repeated with the following differences. The porous membrane was a porous polypropylene film having an effective pore diameter of about 40 nm, a thickness of about 25 μm, and a porosity of about 0.45. The porous polypropylene film is available under the trade name "Celgard 2500" from Calanese Corporation of Summit, N.J.
The feed solution was a solution of acetic acid in water with an acetic acid concentration of 4.2×10-4 gmol/ml. The extractant was xylene.
The pressure vessel charged with xylene was pressurized to a pressure above ambient atmospheric pressure just great enough to cause a flow rate of about 32 ml/min of xylene through the extraction cell. The pressure and flow rate of the aqueous feed solution were substantially the same as Example 1.
After the steady state was reached essentially no droplets of a xylene phase were observed in the aqueous solution discharged from the extraction cell and no droplets of a water phase were observed in the xylene solution discharged from the extraction cell.
The concentration of acetic acid in the xylene discharged from the extraction cell after a steady state was reached was found to be about 2.54×10-7 gmol/ml. The solute transfer coefficient Ko for the membrane was about 19.7×10-4 cm/sec.
EXAMPLE 3
The procedure of Example 1 was repeated with the exceptions noted below.
A porous membrane of porous polytetrafluoroethylene(PTFE) was used. The porous PTFE had an effective pore diameter of about 20 nm, a thickness of about 50 μm, a porosity of about 0.50, and a minimum pressure for water entry of about 2.4 MPa. The porous PFTE film was available under the trade name "Goretex" from W. L. Gore and Associates of Elton, Md.
The feed solution was solution of acetic acid in water having an acetic acid concentration of about 4.2×10-4 gmol/ml. The extractant was xylene. The flow rate of xylene through the extraction cell was about 50 ml/min and the pressure of the xylene was only slightly above ambient atmospheric pressure. The flow rate of the aqueous feed solution was about 22 ml/min and the pressure was about 69 kPa above ambient atmospheric pressure.
After a steady state was reached, essentially no droplets of a xylene phase were observed in the aqueous solution discharged from the extraction cell and essentially no droplets of a water phase were observed in the xylene solution discharged from the extraction cell.
The concentration of acetic acid in the xylene discharged from the extraction cell after a steady stake was reached was found to be about 1.2×10-7 gmol/ml.
The solute transfer coefficient Ko was about 14.9×10-4 cm/sec.
EXAMPLE 4
The procedure of Example 1 was repeated with the following exceptions.
The porous membrane was porous PTFE having an effective pore diameter of about 200 nm, a thickness of about 63 μm, a porosity of about 0.78 and a minimum pressure for water entry of about 280 kPa. The porous film had a backing of nonwoven polyester fabric. The film was available under the trade name "Goretex" from W. L. Gore and Associates of Elton, Md.
The feed solution used was acetic aced in water having an acetic acid concentration of about 4.2×10-4 gmol/ml. The extractant was pure xylene. The volume flow rate of the xylene through the extraction all was about 28 ml/min The pressure of the xylene was only slightly greater than ambient atmospheric pressure. The volume flow rate of the aqueous feed solution through the extraction cell was about 20 ml/min. The pressure on the feed solution was about 110 kPa above ambient atmospheric pressure.
After a steady state was reached, essentially no droplets of a xylene phase were observed in the aqueous solution discharged from the extraction cell and essentially no droplets of a water phase were observed in the xylene solution discharged from the extraction cell.
The concentration of acetic acid in the xylene solution discharged from the extraction cell after a steady state was achieved was found to be about 4.12×10-7 gmol/ml. The solute transfer coefficient Ko was found to be about 28×10-4 cm/sec.
EXAMPLE 5
The procedure of Example 1 was repeated with the following exceptions.
A hydrophilic porous membrane of porous cellulose acetate was used. The porous membrane had an effective pore diameter of about 200 nm and a thickness of about 130 μm. The porous membrane was available under the trade name "Milipore EG" from Milipore Corporation at Bedford, Mass.
A feed solution of acetic acid in water with an acetic acid concentration of about 4×10-4 gmol/ml was used. The extractant was pure xylene.
The extractant had a volume flow rate of about 60 ml/min and a pressure of about 55 kPa above ambient atmospheric pressure.
The feed solution had a volume flow rate of about 30 ml/min and a pressure of only slightly above ambient atmospheric pressure. The feed solution was directed through the fluid-chamber depression of the second extraction cell housing block, which contained the disk of screening for support. The aqueous feed solution was introduced into the extraction cell before the xylene in order to allow the feed solution to wet the hydrophilic membrane.
After a steady state was reached, essentially no droplets of a xylene phase were observed in the aqueous solution discharged from the extraction cell and essentially no droplets of a water phase were observed in the xylene solution discharged from the extraction cell.
The concentration of the acetic acid in the xylene solution discharged from the extraction cell after a steady state was achieved was found to be about 1.6×10-7 gmol/ml The solute transfer coefficient Ko was found to be about 24×10-4 cm/sec.
EXAMPLE 6
The procedure of example 1 was followed with the following exceptions.
The porous membrane of example 1 and the feed solution of example 2 were used. The extractant was methylisobutylketone (MIBK).
The volume flow rate of the MIBK through the extraction cell was about 22 ml/min. The pressure of the MIBK extractant was only slightly above ambient atmospheric pressure. The volume flow rate of the feed solution was about 33 ml/min and the pressure of the feed solution was about 140 kPa above ambient atmospheric pressure.
After a steady state was reached, essentially no droplets of an MIBK phase were observed in the aqueous solution discharged from the extraction cell and essentially no droplets of a water phase were observed in the MIBK solution discharged from the extraction cell.
The concentration of acetic acid in the MIBK solution discharged from the extraction cell after a steady state was achieved was found to be about 3.9×10-6 gmol/ml. The solute transfer coefficient Ko was found to be about 5×10-4 cm/sec.
The results of examples 1-6 are summarized in the following Table I which follows.
It is not intended to limit the present invention to the specific embodiments disclosed above. It is recognized that changes may be made in the processes and apparatus specifically described herein without departing from the scope and teachings of the instant invention. For example, the screens 80 and 82 in the extraction cell 42 of FIG. 2 can be placed on the opposite side of the membranes if the feed solution and the back extractant preferentially wet the membranes 46 and 48. It is intended to encompass all other embodiments, alternatives and modifications consistent with the present invention.
                                  TABLE I                                 
__________________________________________________________________________
Extraction of Acetic Acid from Water into an Organic Extractant           
               Feed Solution     Extractant              Solute           
      Membrane Inlet HAc               Outlet HAc        Transfer         
      Polymer  Conc.                   Conc.             Coef.            
Example                                                                   
      Pore size (μm)                                                   
               (gmol/cm.sup.3)                                            
                     Flow Rate                                            
                           Pressure    (gmol/cm.sup.3)                    
                                             Flow Rate                    
                                                   Pressure               
                                                         (cm/sec)         
No.   Thickness (μm)                                                   
               × 10.sup.-4                                          
                     (cm.sup.3 /min)                                      
                           (kPa) Compound                                 
                                       × 10.sup.-7                  
                                             (cm.sup.3 /min)              
                                                   (kPa) × 10.sup.-4
__________________________________________________________________________
1.    Polypropylene                                                       
               5.6   20    280   xylene                                   
                                       4.66  20    0+    17.3             
      0.02                                                                
      25                                                                  
2.    Polypropylene                                                       
               4.2   20    280   xylene                                   
                                       2.54  32    0+    19.7             
      0.04                                                                
      25                                                                  
3.    PTFE,    4.2   22     59   xylene                                   
                                       1.23  50    0+    14.9             
      0.04                                                                
      50                                                                  
4.    PTFE*,   4.2   20    110   xylene                                   
                                       4.12  28    0+    28.0             
      0.2                                                                 
      63                                                                  
5.    Celluose Acetate                                                    
               4.0   30    0+    xylene                                   
                                       1.60  60    55    24.0             
      0.2.                                                                
      130                                                                 
6.    Polypropylene                                                       
               4.2   33    140   MIBK  39.0  22    0+    5.00             
      0.02                                                                
      25                                                                  
__________________________________________________________________________
 *Backing of nonwoven polyester fibers                                    

Claims (12)

    I claim: .[.1. An immobilized-interface solute-transfer unit for transferring a solute from a feed solution to an extractant liquid, the solute-transfer unit comprising:
  1. to changes in a control signal at the valve control input..]. .[.7. The immobilized-interface solute-transfer unit according to claim 1 in which the extractant inlet port is connected to a source of extractant liquid..]. .[.8. A membrane solute-transfer unit for transferring solute from a liquid feed solution to a liquid extractant, the solute-transfer unit comprising:
    (a) a solute-transfer unit housing having feed-solution inlet port means for introducing a feed solution into an interior of the housing and feed solution outlet port means for discharging the feed solution from the interior of the housing, the housing having extractant inlet and outlet port means for introducing and discharging an extractant from the interior of the housing;
    (b) a plurality of hollow solute-transfer tubes, the solute-transfer tubes extending through the interior of the solute-transfer unit housing from the feed-solution inlet port means to the feed-solution outlet port means, the walls of the tubes being made of a porous membrane material, the porous membrane material including pores having effective pore diameters in the range of from about 7 nm to about 10 μm, the porous membrane material being preferentialy wettable by one of the feed-solution and liquid extractant interiors of the tubes communicating at an inlet end with the feed-solution inlet port means for receiving the feed-solution and at an outlet end with the feed solution outlet port means for discharging the feed solution; and
    (c) pressure difference control means for maintaining a difference between a liquid pressure of a feed solution in the interior of the solute-transfer tubes and a liquid pressure of an extractant in the interior of the separation unit housing exterior of the solute-transfer tubes substantially within a predetermined pressure range so that an interface between the feed solution and the extractant is substantially immobilized at the porous membrane wall of the solute-transfer tubes to effectively prevent the formation of a dispersion of feed solution and extractant in either the interior of the solute-transfer tubes or in the interior of the separation unit housing exterior of the solute-transfer tubes..]. .[.9. The membrane solute-transfer unit according to claim 8 in which the extractant inlet and outlet port means in connected to a source of liquid extractant..]. .[.10. A membrane solute-transfer unit for transferring solute from a liquid feed solution to a liquid extractant, the solute-transfer unit comprising:
    (a) a solute-transfer unit housing having extractant inlet port means for introducing a liquid extractant into an interior of the housing and extractant outlet port means for discharging the extractant from the interior of the housing, the housing having feed-solution inlet and outlet port means for introducing and discharging a feed solution from the interior of the housing;
    (b) a plurality of hollow solute-transfer tubes, the solute-transfer tubes extending through the interior of the solute-transfer unit housing from the extractant inlet port means to the extractant outlet port means, the walls of the tubes being made of a porous membrane material, the porous membrane material including pores having effective pore diameters in the range of from about 7 mm to about 10 μm, the porous membrane material being preferentially wettable by one of the feed-solution and liquid extractant interiors of the tubes communicating at an inlet end with the extractant inlet port means for receiving the liquid extractant and at an outlet end with the extractant outlet port means for discharging the extractant; and
    (c) pressure difference control means for maintaining a difference between a liquid pressure of the extractant in the interior of the solute-transfer tubes and a liquid pressure of the feed solution in the interior of the separation unit housing exterior of the solute-transfer tubes substantially within a predetermined pressure range so that an interface between the feed solution and the extractant is substantially immobilized at the porous membrane wall of the solute-transfer tubes to effectively prevent the formation of a dispersion of feed solution and extractant in either the interior of the solute-transfer tubes or in the interior of the separation unit housing exterior of the solute-transfer tubes..]. .[.11. The membrane solute-transfer unit according to claim 7 in which the pores of the porous membrane material of the solute-transfer tubes are of a size substantially to prevent cellular debris in a feed solution from passing from the feed solution exterior of the solute-transfer tubes to the interior of the solute-transfer tubes, and the solute-transfer unit further comprises:
    (d) gas-permeable membrane means for introducing oxygen into the feed solution in the interior of the separation-unit housing..]. .[.12. The membrane solute-transfer unit according to claim 10 in which the extractant inlet port means is connected to a source of liquid
  2. extractant..]. 13. An immobilized-interface solute-transfer unit for transferring a solute from a feed solution to an extractant liquid, the solute-transfer unit comprising:
    (a) A fluid-tight housing;
    (b) a first porous membrane located in and connected to the housing, the first porous membrane being preferentially wettable by one of the feed solution and the extractant liquid, the first porous membrane dividing the housing into a feed solution chamber and an extractant chamber, the housing having a feed solution inlet port and a feed solution outlet port which communicate with the feed solution chamber and an extractant inlet port and an extractant outlet port which communicate with the extractant chamber;
    (c) feed-solution/extractant pressure difference control means for maintaining a difference between a liquid pressure of a feed solution in the feed solution chamber and a liquid pressure of an extractant in the extractant chamber substantially within a predetermined pressure range so that an interface between the feed solution and the extractant is substantially immobilized at the first porous membrane to effectively prevent the formation of a dispersion of feed solution and extractant in either chamber on opposing sides of the membrane;
    (d) a second porous membrane located in and connected to the housing the second porous membrane being preferentially wettable by one of the extractant liquid and a back-extractant, the second porous membrane being located in the extractant chamber and dividing the chamber into an intermediate extractant subchamber and a back extractant subchamber, the extractant inlet and outlet ports being in communication with the intermediate extractant subchamber, the housing having a back extractant inlet port and a back extractant outlet port which communicate with the back extractant subchamber; and
    (e) back-extractant/pressure difference control means for maintaining a difference between a liquid pressure of a back extractant in the back extractant subchamber and a liquid pressure of an intermediate extractant in the intermediate extractant subchamber substantially within a predetermined pressure range so that the interface between the back extractant and the intermediate extractant is substantially immobilized at the second porous membrane to effectively prevent the formation of a dispersion of back-extractant and extractant in either subchamber on
  3. opposing sides of the second porous membrane. 14. The immobilized-interface solute-transfer unit according to claim 13 in which the extractant inlet port is connected to a source of extractant liquid.
  4. . The membrane-separation unit according to claim 13 in which
    (b.1) The porous membrane is in the shape of a hollow tube, the interior of the tube defining a feed-solution chamber; and
    (d.1) the second porous membrane is in the shape of a hollow tube, the
  5. interior of the tube defining a back extractant subchamber. 16. A membrane solute-transfer unit for transferring solute from a liquid feed solution to a liquid extractant, the solute-transfer unit comprising:
    (a) a solute-transfer unit housing having extractant inlet port means for introducing a liquid extractant into an interior of the housing and extractant outlet port means for discharging the extractant from the interior of the housing, the housing having feed-solution inlet and outlet port means for introducing and discharging a feed solution from the interior of the housing, and the housing having auxiliary-extractant inlet port means for introducing a liquid auxiliary extractant into the interior of the housing and auxiliary-extractant outlet port means for discharging the auxiliary extractant from the interior of the housing;
    (b) a plurality of hollow solute-transfer tubes, the solute-transfer tubes extending through the interior of the solute-transfer unit housing from the extractant inlet port means to the extractant outlet port means, the walls of the tubes being made of a porous membrane material the porous membrane material being preferentially wettable by one of the feed solution and the extractant liquid, interiors of the tubes communicating at an inlet end with the extractant inlet port means for receiving the liquid extractant and at an outlet end with the extractant outlet port means for discharging the extractant;
    (c) extractant/feed-solution pressure difference control means for maintaining a difference between a liquid pressure of the extractant in the interior of the solute-transfer tubes and a liquid pressure of the feed solution in the interior of the separation unit housing exterior of the solute-transfer tubes substantially within a predetermined pressure range so that an interface between the feed solution and the extractant is substantially immobilized at the porous membrane wall of the solute-transfer tubes to effectively prevent the formation of a dispersion of feed solution and extractant in either the interior of the solute-transfer tubes or in the interior of the separation unit housing exterior of the solute-transfer tubes;
    (d) a plurality of hollow auxiliary-extractant solute-transfer tubes, the auxiliary extractant solute-transfer tubes extending through the interior of the solute-transfer unit housing from the auxiliary-extractant inlet port means to the auxiliary-extractant outlet port means, the wall of the tubes being made of a porous membrane material, the porous membrane material being preferentially wettable by one of the auxiliary-extractant and the feed solution, interiors of the tubes communicating at an inlet end with the auxiliary-extractant inlet port means for receiving the auxiliary extractant and at an outlet end with the auxiliary-extractant outlet port means for discharging the auxiliary extractant; and
    (e) auxiliary-extractant/feed-solution pressure-difference control means for maintaining a difference between a liquid pressure of the auxiliary-extractant in the interior of the auxiliary-extractant solute-transfer tubes and a liquid pressure of the feed solution in the interior of the separation unit housing exterior of the auxiliary-extractant solute-transfer tubes substantially within a predetermined pressure range so that an interface between the feed solution and the auxiliary extractant is substantially immobilized at the porous membrane wall of the auxiliary-extractant solute-transfer tubes to effectively prevent the formation of a dispersion of feed solution and auxiliary-extractant in either the interior of the auxiliary-extractant solute-transfer tube or in the interior of the separation unit housing
  6. exterior of the auxiliary-extractant solute-transfer tubes. 17. The membrane solute transfer unit according to claim 16 in which the extractant inlet and outlet port mans is connected to a source of liquid
  7. extractant. 18. A membrane solute transfer unit for transferring solute from a liquid feed solution to a liquid extractant, the solute-transfer unit comprising:
    a solute-transfer unit housing having feed-solution inlet port means for introducing a feed solution into an interior of the housing and feed solution outlet port means for discharging the feed solution from the interior of the housing, the housing having extractant inlet and outlet port means for introducing and discharging an extractant from the interior of the housing, the housing having back-extractant inlet port means for introducing a liquid back extractant into the interior of the housing and back-extractant outlet port means for discharging the back extractant from the interior of the housing;
    (b) a plurality of hollow solute-transfer tubes, the solute-transfer tubes extending through the interior of the solute-transfer unit housing from the feed-solution inlet port means to the feed-solution outlet port means, the walls of the tubes being made of a porous membrane material, the porous membrane material being preferentially wettable by one of the feed solution and the extractant liquid, interiors of the tubes communicating at an inlet end with the feed-solution inlet port means for receiving the feed-solution and at an outlet end with the feed solution outlet port means for discharging the feed solution;
    (c) feed-solution/extractant pressure difference control means for maintaining a difference between a liquid pressure or a feed solution in the interior of the solute-transfer tubes and a liquid pressure of an extractant in the interior of the separation unit housing exterior of the solute-transfer tubes substantially within a predetermined pressure range so that an interface between the feed solution and the extractant is substantially immobilized at the porous membrane wall of the solute-transfer tubes to effectively prevent the formation of a dispersion of feed solution and extractant in either the interior of the solute-transfer tubes or in the interior of the separation unit housing exterior of the solute-transfer tubes;
    (d) a plurality of hollow back-extractant solute-transfer tubes, the back-extractant solute-transfer tubes extending through the interior of the solute-transfer unit housing from the back-extractant inlet port means to the back-extractant outlet port means, the walls of the tubes being made of a porous membrane material the porous membrane material being preferentially wettable by one of the extractant liquid and the back-extractant, the back-extractant solute-transfer tubes commingling with the solute-transfer tubes, interiors of the back-extractant solute-transfer tubes communicating at an inlet end with the back-extractant inlet port means for receiving the back-extractant liquid and at an outlet end with the back-extractant outlet port means for discharging the back extractant; and
    (e) back-extractant/extractant pressure difference control means for maintaining a difference between a liquid pressure of a back-extractant liquid in the interior of the back-extractant solute-transfer tubes and a liquid pressure of the extractant in the interior of the separation unit housing exterior of the back-extractant solute-transfer tubes substantially within the predetermined pressure range so that an interface between the back extractant and the extractant is substantially immobilized at the porous membrane wall of the back-extractant solute-transfer tubes to effectively prevent the formation of a dispersion of back-extractant and extractant in either the interior of the back-extractant solute-transfer tubes or in the interior of the separation
  8. unit housing exterior of the back-extractant solute-transfer tubes. 19. The membrane solute-transfer unit according to claim 18 in which the extractant inlet port means is connected to a source of liquid extractant and the auxiliary-extractant inlet port means is connected to a source of
  9. liquid auxiliary extractant. .Iadd.20. An immobilized-interface solute-transfer unit for transferring a solute from a feed solution to an extractant liquid, the solute-transfer unit comprising:
    (a) a fluid-tight housing;
    (b) a porous membrane located in and connected to the housing, the porous membrane including pores having effective pore diameters in the range of from about 20 nm to about 10 μm, the porous membrane being preferentially wettable by one of the feed-solution and liquid extractant, the porous membrane dividing the housing into a feed solution chamber and an extractant chamber, the housing having a feed solution inlet port and a feed solution outlet port which communicate with the feed solution chamber and an extractant inlet port and an extractant outlet port which communicate with the extractant chamber;
    (c) pressure difference control means for maintaining a difference between a liquid pressure of a feed solution in the feed solution chamber and a liquid pressure of an extractant in the extractant chamber substantially within a predetermined pressure range so that an interface between the feed solution and the extractant is substantially immobilized at the membrane, to effectively prevent the formation of a dispersion of feed solution and extractant in either chamber on opposing sides of the membrane..Iaddend. .Iadd.21. The membrane solute-transfer unit according to claim 20 in which the porous membrane is in the shape of a hollow tube, the interior of the tube defining one of the feed solution chamber and the
  10. extractant chamber..Iaddend. .Iadd.22. The membrane separation unit according to claim 20 in which the porous membrane is composed of a hydrophilic material selected from the group consisting of porous regenerated cellulose, porous cellulose acetate, porous cellulose acetate-nitrate, porous cellulose triacetate, microporous glass and porous porcelain..Iaddend. .Iadd.23. The membrane separation unit according to claim 20 in which the porous membrane is composed of a hydrophobic material selected from the group consisting of porous polyethylene, porous polypropylene and porous polytetrafluoroethylene..Iaddend. .Iadd.24. The membrane-separation unit according to claim 20 in which the porous membrane is approximately planar in shape and the unit further comprises:
    (d) a membrane reinforcing screen connected to the housing and located adjacent to the porous membrane on a side of the membrane facing a chamber maintained in operation at a pressure lower than the pressure of the chamber on the opposing side of the membrane..Iaddend. .Iadd.25. The membrane unit according to claim 20 in which the pressure control means includes:
    (c.1) a feed-solution pressure sensor in communication with the feed-solution chamber for detecting a liquid pressure in the chamber;
    (c.2) an extractant pressure sensor in communication with the extractant chamber for detecting a liquid pressure in the chamber;
    (c.3) a pressure-difference regulator having a head pressure-sensor input, a base pressure-sensor input and a control signal output, the head pressure-sensor input being connected to one of the feed-solution pressure sensor and the extractant pressure sensor and the base pressure-sensor input being connected to the other of the feed-solution pressure sensor and the extractant pressure sensor, the pressure-difference regulator being adapted to generate a pressure control signal at the control-signal output which varies in response to changes in the difference between the pressure sensed at the head pressure-sensor input and the base pressure-sensor input; and
    (c.4) a pressure control valve having a valve control input connected to the control-signal output of the pressure-difference regulator, the pressure control valve being in fluid communication with one of the feed solution chamber and the extractant chamber and being adapted to change the liquid pressure in the chamber with which it communicates in response to changes in a control signal at the valve control input..Iaddend. .Iadd.26. The immobilized-interface solute-transfer unit according to claim 20 in which the extractant inlet port is connected to a source of extractant liquid..Iaddend. .Iadd.27. A membrane solute-transfer unit for transferring solute from a liquid feed solution to a liquid extractant, the solute-transfer unit comprising:
    (a) A solute-transfer unit housing having feed-solution inlet port means for introducing a feed solution into an interior of the housing and feed solution outlet port means for discharging the feed solution from the interior of the housing, the housing having extractant inlet and outlet port means for introducing and discharging an extractant from the interior of the housing;
    (b) a plurality of hollow solute-transfer tubes, the solute-transfer tubes extending through the interior of the solute-transfer unit housing from the feed-solution inlet port means to the feed-solution outlet port means, the walls of the tubes being made of a porous membrane material, the porous membrane material including pores having effective pore diameters in the range of from about 20 nm to about 10 μm, the porous membrane material being preferentially wettable by one of the feed-solution and liquid extractant interiors of the tubes communicating at an inlet end with the feed-solution inlet port means for receiving the feed-solution and at an outlet end with the feed solution outlet port means for discharging the feed solution; and
    (c) pressure difference control means for maintaining a difference between a liquid pressure of a feed solution in the interior of the solute-transfer tubes and a liquid pressure of an extractant in the interior of the separation unit housing exterior of the solute-transfer tubes substantially within a predetermined pressure range so that an interface between the feed solution and the extractant is substantially immobilized at the porous membrane wall of the solute-transfer tubes to effectively prevent the formation of a dispersion of feed solution and extractant in either the interior of the solute-transfer tubes or in the interior of the separation unit housing exterior of the solute-transfer
  11. tubes..Iaddend. .Iadd.28. The membrane solute-transfer unit according to claim 27 in which the extractant inlet and outlet port means in connected
  12. to a source of liquid extractant..Iaddend. .Iadd.29. A membrane solute-transfer unit for transferring solute from a liquid feed solution to a liquid extractant, the solute-transfer unit comprising:
    (a) a solute-transfer unit housing having extractant inlet port means for introducing a liquid extractant into an interior of the housing and extractant outlet port means for discharging the extractant from the interior of the housing, the housing having feed-solution inlet and outlet port means for introducing and discharging a feed solution from the interior of the housing;
    (b) a plurality of hollow solute-transfer tubes, the solute-transfer tubes extending through the interior of the solute-transfer unit housing from the extractant inlet port means to the extractant outlet port means, the walls of the tubes being made of a porous membrane material, the porous membrane material including pores having effective pore diameters in the range of from about 20 nm to about 10 μm, the porous membrane material being preferentially wettable by one of the feed-solution and liquid extractant interiors of the tubes communicating at an inlet end with the extractant inlet port means for receiving the liquid extractant and at an outlet end with the extractant outlet port means for discharging the extractant; and
    (c) pressure difference control means for maintaining a difference between a liquid pressure of the extractant in the interior of the solute-transfer tubes and a liquid pressure of the feed solution in the interior of the separation unit housing exterior of the solute-transfer tubes substantially within a predetermined pressure range so that an interface between the feed solution and the extractant is substantially immobilized at the porous membrane wall of the solute-transfer tubes to effectively prevent the formation of a dispersion of feed solution and extractant in either the interior of the solute-transfer tubes or in the interior of the separation unit housing exterior of the solute-transfer tubes..Iaddend. .Iadd.30. The membrane solute-transfer unit according to claim 29 in which the extractant inlet port means is connected to a source of liquid extractant..Iaddend.
US07/781,864 1984-08-28 1991-10-24 Immobilized-interface solute-transfer apparatus Expired - Lifetime USRE34828E (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US07/781,864 USRE34828E (en) 1984-08-28 1991-10-24 Immobilized-interface solute-transfer apparatus

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US06/644,895 US4789468A (en) 1984-08-28 1984-08-28 Immobilized-interface solute-transfer apparatus
US07/781,864 USRE34828E (en) 1984-08-28 1991-10-24 Immobilized-interface solute-transfer apparatus

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US06/644,895 Reissue US4789468A (en) 1984-08-28 1984-08-28 Immobilized-interface solute-transfer apparatus

Publications (1)

Publication Number Publication Date
USRE34828E true USRE34828E (en) 1995-01-17

Family

ID=24586787

Family Applications (2)

Application Number Title Priority Date Filing Date
US06/644,895 Ceased US4789468A (en) 1984-08-28 1984-08-28 Immobilized-interface solute-transfer apparatus
US07/781,864 Expired - Lifetime USRE34828E (en) 1984-08-28 1991-10-24 Immobilized-interface solute-transfer apparatus

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US06/644,895 Ceased US4789468A (en) 1984-08-28 1984-08-28 Immobilized-interface solute-transfer apparatus

Country Status (2)

Country Link
US (2) US4789468A (en)
CA (1) CA1271428A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0771585A2 (en) 1995-11-06 1997-05-07 Hoechst Celanese Corporation Method for solvent extraction using a dual-skinned asymmetric microporous membrane
US5753797A (en) * 1995-04-09 1998-05-19 Cerberus Ag Photo-acoustic gas sensor and its manufacture and use
US6214300B1 (en) 1994-12-02 2001-04-10 The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration Microencapsulation and electrostatic processing device
US20040181101A1 (en) * 2003-03-13 2004-09-16 3M Innovative Properties Company Method for obtaining ethanol
US7105089B2 (en) 2003-03-13 2006-09-12 3M Innovative Properties Company Liquid—liquid extraction system and method

Families Citing this family (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4921612A (en) * 1985-10-22 1990-05-01 The Trustees Of Stevens Institute Of Technology Asymmetrically-wettable porous membrane process
US4966707A (en) * 1986-05-13 1990-10-30 Celanese Corporation Liquid/liquid extractions with microporous membranes
US4976867A (en) * 1989-04-05 1990-12-11 Hoechst Celanese Corporation Systems and methods for predetermining maximum pressure differentials for microporous hollow fibers employed in liquid-liquid extractions
US5252220A (en) * 1989-09-25 1993-10-12 Symbiotech Incorporated Preparation of analytical samples by liquid-liquid extraction using microporous hollow-fiber membranes
US5100555A (en) * 1990-06-15 1992-03-31 Matson Stephen L Method and system for removing radon from radon containing water
US5194158A (en) * 1990-06-15 1993-03-16 Matson Stephen L Radon removal system and process
US5041227A (en) * 1990-10-09 1991-08-20 Bend Research, Inc. Selective aqueous extraction of organics coupled with trapping by membrane separation
US5160627A (en) * 1990-10-17 1992-11-03 Hoechst Celanese Corporation Process for making microporous membranes having gel-filled pores, and separations methods using such membranes
US5449457A (en) * 1991-04-22 1995-09-12 Hoechst Celanese Corporation Liquid membrane modules with minimal effective membrane thickness and methods of making the same
US5169529A (en) * 1991-04-22 1992-12-08 Hoechst Celanese Corporation Liquid membrane modules with minimal effective membrane thickness and methods of making the same
US5507949A (en) * 1992-03-20 1996-04-16 Monsanto Company Supported liquid membrane and separation process employing same
DK0561760T3 (en) * 1992-03-20 1999-05-25 Monsanto Co Extraction of organic compounds from aqueous solutions
IL101906A0 (en) * 1992-05-18 1992-12-30 Yissum Res Dev Co Extraction of electrolytes from aqueous solutions
US5306831A (en) * 1992-10-15 1994-04-26 Shell Oil Company Sorbitan ester purification process
AU5608294A (en) * 1992-11-27 1994-06-22 Global Water Technologies, Inc. Desalinization system
US5391298B1 (en) * 1993-03-05 1997-10-28 Minnesota Mining & Mfg Method for performing a solid-phase extraction under pressurized conditions
US5328610A (en) * 1993-06-15 1994-07-12 Integrated Process Technologies Self-supported low pressure drop hollow fiber membrane panel and contactor module
NL9301535A (en) * 1993-09-06 1995-04-03 Tno A method for removing acidic components, such as mercaptans, from liquid hydrocarbons, such as a light oil fraction.
US6165253A (en) * 1994-05-23 2000-12-26 New Jersey Institute Of Technology Apparatus for removal of volatile organic compounds from gaseous mixtures
US5637224A (en) * 1994-09-14 1997-06-10 New Jersey Institute Of Technology Hollow fiber contained liquid membrane pervaporation for removal of volatile organic compounds from aqueous solutions
AU699883B2 (en) * 1994-10-22 1998-12-17 Central Research Laboratories Limited Method and apparatus for diffusive transfer between immiscible fluids
WO1996012540A1 (en) * 1994-10-22 1996-05-02 Central Research Laboratories Limited Method and apparatus for diffusive transfer between immiscible fluids
US5580452A (en) * 1994-12-02 1996-12-03 Lsr Technologies, Inc. Moving liquid membrane modules
US5868935A (en) * 1995-03-15 1999-02-09 New Jersey Institute Of Technology Method and apparatus for extraction and recovery of ions from solutions
DE19608463B4 (en) * 1996-03-02 2008-08-14 Sasol- Lurgi Technology Co.(Pty)Ltd. Process for extracting phenols from a phenol-containing wastewater by means of a solvent mixture
GB9608129D0 (en) * 1996-04-19 1996-06-26 Central Research Lab Ltd Method and apparatus for diffusive transfer between immiscible fluids
US6296767B1 (en) * 1996-04-19 2001-10-02 British Nuclear Fuels Plc Method and apparatus for diffusive transfer between immiscible fluids
NL1003026C2 (en) * 1996-05-03 1997-11-06 Tno Reactor for conducting gas phase / liquid phase / solid phase reactions, as well as a method for conducting such reactions using this reactor.
US5993515A (en) * 1996-05-14 1999-11-30 New Jersey Institute Of Technology Apparatus and process for selectively removing a component from a multicomponent aqueous solution by pervaporation
US5753009A (en) * 1996-05-14 1998-05-19 New Jersey Institute Of Technology Method and apparatus for selectively removing a component from a multicomponent gas/vapor mixture
GB9617586D0 (en) * 1996-08-22 1996-10-02 Ea Tech Ltd Method and apparatus for extracting metal ions from aqueous solutions
US6086769A (en) * 1996-09-16 2000-07-11 Commodore Separation Technologies, Inc. Supported liquid membrane separation
US6165370A (en) * 1998-01-21 2000-12-26 Voith Sulzer Paper Technology North America, Inc. Pressure screen monitoring apparatus and method
US6379973B1 (en) * 1999-03-05 2002-04-30 The United States Of America As Represented By The Department Of Health And Human Services Chromatographic separation apparatus and method
US6485650B1 (en) * 2000-08-28 2002-11-26 Facilichem, Inc. Liquid membrane separation of enantiomers
JP2002361002A (en) * 2001-06-04 2002-12-17 Minolta Co Ltd Extraction method and extraction apparatus, and separation method and separation apparatus
US7279215B2 (en) * 2003-12-03 2007-10-09 3M Innovative Properties Company Membrane modules and integrated membrane cassettes
US20050187308A1 (en) * 2004-02-20 2005-08-25 Korea Advanced Institute Of Science And Technology Method of preparing photopolymer with enhanced optical quality using nanoporous membrane and photopolymer prepared by the same
CA2634617A1 (en) * 2005-12-27 2007-07-05 Shell International Research Maatschappij B.V. Gas separation apparatus
CA2653639C (en) * 2006-06-14 2012-08-28 Ram Lavie Method and apparatus for liquid-liquid extraction
EP2188216B1 (en) * 2007-07-26 2018-04-25 FPInnovations Process for treating pulp mill condensates using a hollow fiber contactor
US20120247327A1 (en) * 2010-09-27 2012-10-04 Conocophillips Company Hollow-fiber membrane contactors
US10342909B2 (en) 2013-01-11 2019-07-09 The Charles Stark Draper Laboratory Inc. Systems and methods for increasing convective clearance of undesired particles in a microfluidic device
US10603419B2 (en) 2013-01-11 2020-03-31 The Charles Stark Draper Laboratories, Inc. Systems and methods for increasing convective clearance of undesired particles in a microfluidic device
US10478543B2 (en) 2013-01-11 2019-11-19 The Charles Stark Draper Laboratory, Inc. Systems and methods for increasing convective clearance of undesired particles in a microfluidic device
WO2016196773A1 (en) * 2015-06-02 2016-12-08 Conocophillips Company Method of removing hydrogen sulfide from water

Citations (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2365457A (en) * 1940-05-21 1944-12-19 Hornkem Corp Dialysis
US3396510A (en) * 1966-08-15 1968-08-13 Gen Electric Liquid membranes for use in the separation of gases
US3422008A (en) * 1963-10-24 1969-01-14 Dow Chemical Co Wound hollow fiber permeability apparatus and process of making the same
US3447286A (en) * 1967-08-02 1969-06-03 Gen Electric Totally enclosed liquid permselective membrane
US3556990A (en) * 1967-12-05 1971-01-19 Arnold G Gulko Reverse osmosis purification of hydrocarbon fuels
US3676220A (en) * 1969-02-27 1972-07-11 Gen Electric Facilitated transport liquid membrane
US3719590A (en) * 1970-12-17 1973-03-06 Exxon Research Engineering Co Liquid membrane system for separation of components of liquid mixtures
US3770842A (en) * 1972-06-29 1973-11-06 Standard Oil Co Method of separating aliphatically unsaturated hydrocarbons by contacting said hydrocarbons with a solid water-insoluble, semi-permeable film membrane
US3799873A (en) * 1968-04-19 1974-03-26 Hydronautics Artificial kidney
US3800506A (en) * 1972-08-23 1974-04-02 Standard Oil Co Process
US3823529A (en) * 1973-02-23 1974-07-16 Standard Oil Co Process for separating carbon monoxide
US3911080A (en) * 1971-09-10 1975-10-07 Wright H Dudley Air pollution control
US3917526A (en) * 1974-04-04 1975-11-04 Universal Oil Prod Co Combined foam flotation and membrane separation processing
US3925037A (en) * 1974-02-04 1975-12-09 Gen Electric High pressure membrane package construction
US3951789A (en) * 1973-10-11 1976-04-20 Allied Chemical Corporation Novel high diffusivity membranes
US3956112A (en) * 1973-01-02 1976-05-11 Allied Chemical Corporation Membrane solvent extraction
US3957504A (en) * 1974-11-11 1976-05-18 Allied Chemical Corporation Membrane hydro-metallurgical extraction process
US3980605A (en) * 1972-09-13 1976-09-14 Standard Oil Company Semi-permeable membrane compositions based on blends of polyamides and polyvinyl alcohols
US4000065A (en) * 1974-11-18 1976-12-28 Basf Wyandotte Corporation Method and apparatus for purifying aqueous streams contaminated with organic materials
US4005012A (en) * 1975-09-22 1977-01-25 The United States Of America As Represented By The Secretary Of The Interior Semipermeable membranes and the method for the preparation thereof
US4014665A (en) * 1974-10-07 1977-03-29 Standard Oil Company (Indiana) Membrane process and product
US4015955A (en) * 1975-02-05 1977-04-05 Standard Oil Company Fluid separation process and membrane
US4062882A (en) * 1974-05-16 1977-12-13 Lever Brothers Company Process for refining crude glyceride oils by membrane filtration
US4106920A (en) * 1973-03-12 1978-08-15 Standard Oil Company (Indiana) Method of making a semi-permeable, essentially water-insoluble, hydrophilic nylon membrane and resultant product
US4115514A (en) * 1975-07-28 1978-09-19 General Electric Company Separation of hydrogen sulfide from gas mixture including carbon dioxide
US4117079A (en) * 1976-06-11 1978-09-26 Exxon Research & Engineering Co. Removal of a gas component present in a gaseous stream
US4119408A (en) * 1977-06-22 1978-10-10 General Electric Company Apparatus for maintaining the separation efficiency of immobilized liquid membranes in gas separation
US4198293A (en) * 1975-03-22 1980-04-15 Hitachi, Ltd. Tubular membrane separation process and apparatus therefor
US4214020A (en) * 1977-11-17 1980-07-22 Monsanto Company Processes for coating bundles of hollow fiber membranes
US4220535A (en) * 1978-08-04 1980-09-02 Monsanto Company Multi-zoned hollow fiber permeator
US4296205A (en) * 1980-02-22 1981-10-20 Verma Dharmvir S Cell culture and continuous dialysis flask and method
US4303068A (en) * 1978-02-28 1981-12-01 Rensselaer Polythechnic Institute Method and apparatus for single pass hemodialysis with high flux membranes and controlled ultrafiltration
US4306946A (en) * 1980-08-18 1981-12-22 General Electric Company Process for acid recovery from waste water
US4326960A (en) * 1979-08-14 1982-04-27 Nitto Electric Industrial Company Ltd. Tubular permselective membrane module and method
US4329224A (en) * 1980-11-14 1982-05-11 General Electric Company Wastewater treatment process
US4366063A (en) * 1981-06-17 1982-12-28 Romec Environmental Research & Development, Inc. Process and apparatus for recovering usable water and other materials from oil field mud/waste pits
US4392960A (en) * 1975-01-27 1983-07-12 A. T. Ramot Plastics, Ltd. Process for the removal of urea from aqueous solutions
US4406752A (en) * 1981-11-12 1983-09-27 General Electric Company Electrowinning of noble metals
US4418148A (en) * 1981-11-05 1983-11-29 Miles Laboratories, Inc. Multilayer enzyme electrode membrane
US4420398A (en) * 1981-08-13 1983-12-13 American National Red Cross Filteration method for cell produced antiviral substances
US4443414A (en) * 1982-08-13 1984-04-17 General Electric Company Process for separation of molybdenum from tungsten leachates
US4445990A (en) * 1981-11-12 1984-05-01 General Electric Company Electrolytic reactor for cleaning wastewater
US4455236A (en) * 1982-12-20 1984-06-19 General Electric Company Method for removing hydrogen sulfide from aqueous streams
US4554069A (en) * 1979-11-15 1985-11-19 Baxter Travenol Laboratories, Inc. Pressure regulator

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3907526A (en) * 1973-04-30 1975-09-23 Peabody Engineering Corp High velocity spray scrubber

Patent Citations (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2365457A (en) * 1940-05-21 1944-12-19 Hornkem Corp Dialysis
US3422008A (en) * 1963-10-24 1969-01-14 Dow Chemical Co Wound hollow fiber permeability apparatus and process of making the same
US3396510A (en) * 1966-08-15 1968-08-13 Gen Electric Liquid membranes for use in the separation of gases
US3447286A (en) * 1967-08-02 1969-06-03 Gen Electric Totally enclosed liquid permselective membrane
US3556990A (en) * 1967-12-05 1971-01-19 Arnold G Gulko Reverse osmosis purification of hydrocarbon fuels
US3799873A (en) * 1968-04-19 1974-03-26 Hydronautics Artificial kidney
US3676220A (en) * 1969-02-27 1972-07-11 Gen Electric Facilitated transport liquid membrane
US3719590A (en) * 1970-12-17 1973-03-06 Exxon Research Engineering Co Liquid membrane system for separation of components of liquid mixtures
US3911080A (en) * 1971-09-10 1975-10-07 Wright H Dudley Air pollution control
US3770842A (en) * 1972-06-29 1973-11-06 Standard Oil Co Method of separating aliphatically unsaturated hydrocarbons by contacting said hydrocarbons with a solid water-insoluble, semi-permeable film membrane
US3800506A (en) * 1972-08-23 1974-04-02 Standard Oil Co Process
US3980605A (en) * 1972-09-13 1976-09-14 Standard Oil Company Semi-permeable membrane compositions based on blends of polyamides and polyvinyl alcohols
US3956112A (en) * 1973-01-02 1976-05-11 Allied Chemical Corporation Membrane solvent extraction
US3823529A (en) * 1973-02-23 1974-07-16 Standard Oil Co Process for separating carbon monoxide
US4106920A (en) * 1973-03-12 1978-08-15 Standard Oil Company (Indiana) Method of making a semi-permeable, essentially water-insoluble, hydrophilic nylon membrane and resultant product
US3951789A (en) * 1973-10-11 1976-04-20 Allied Chemical Corporation Novel high diffusivity membranes
US3925037A (en) * 1974-02-04 1975-12-09 Gen Electric High pressure membrane package construction
US3917526A (en) * 1974-04-04 1975-11-04 Universal Oil Prod Co Combined foam flotation and membrane separation processing
US4062882A (en) * 1974-05-16 1977-12-13 Lever Brothers Company Process for refining crude glyceride oils by membrane filtration
US4014665A (en) * 1974-10-07 1977-03-29 Standard Oil Company (Indiana) Membrane process and product
US3957504A (en) * 1974-11-11 1976-05-18 Allied Chemical Corporation Membrane hydro-metallurgical extraction process
US4000065A (en) * 1974-11-18 1976-12-28 Basf Wyandotte Corporation Method and apparatus for purifying aqueous streams contaminated with organic materials
US4392960A (en) * 1975-01-27 1983-07-12 A. T. Ramot Plastics, Ltd. Process for the removal of urea from aqueous solutions
US4015955A (en) * 1975-02-05 1977-04-05 Standard Oil Company Fluid separation process and membrane
US4198293A (en) * 1975-03-22 1980-04-15 Hitachi, Ltd. Tubular membrane separation process and apparatus therefor
US4115514A (en) * 1975-07-28 1978-09-19 General Electric Company Separation of hydrogen sulfide from gas mixture including carbon dioxide
US4005012A (en) * 1975-09-22 1977-01-25 The United States Of America As Represented By The Secretary Of The Interior Semipermeable membranes and the method for the preparation thereof
US4117079A (en) * 1976-06-11 1978-09-26 Exxon Research & Engineering Co. Removal of a gas component present in a gaseous stream
US4119408A (en) * 1977-06-22 1978-10-10 General Electric Company Apparatus for maintaining the separation efficiency of immobilized liquid membranes in gas separation
US4214020A (en) * 1977-11-17 1980-07-22 Monsanto Company Processes for coating bundles of hollow fiber membranes
US4303068A (en) * 1978-02-28 1981-12-01 Rensselaer Polythechnic Institute Method and apparatus for single pass hemodialysis with high flux membranes and controlled ultrafiltration
US4220535A (en) * 1978-08-04 1980-09-02 Monsanto Company Multi-zoned hollow fiber permeator
US4326960A (en) * 1979-08-14 1982-04-27 Nitto Electric Industrial Company Ltd. Tubular permselective membrane module and method
US4554069A (en) * 1979-11-15 1985-11-19 Baxter Travenol Laboratories, Inc. Pressure regulator
US4296205A (en) * 1980-02-22 1981-10-20 Verma Dharmvir S Cell culture and continuous dialysis flask and method
US4306946A (en) * 1980-08-18 1981-12-22 General Electric Company Process for acid recovery from waste water
US4329224A (en) * 1980-11-14 1982-05-11 General Electric Company Wastewater treatment process
US4366063A (en) * 1981-06-17 1982-12-28 Romec Environmental Research & Development, Inc. Process and apparatus for recovering usable water and other materials from oil field mud/waste pits
US4420398A (en) * 1981-08-13 1983-12-13 American National Red Cross Filteration method for cell produced antiviral substances
US4418148A (en) * 1981-11-05 1983-11-29 Miles Laboratories, Inc. Multilayer enzyme electrode membrane
US4406752A (en) * 1981-11-12 1983-09-27 General Electric Company Electrowinning of noble metals
US4445990A (en) * 1981-11-12 1984-05-01 General Electric Company Electrolytic reactor for cleaning wastewater
US4443414A (en) * 1982-08-13 1984-04-17 General Electric Company Process for separation of molybdenum from tungsten leachates
US4455236A (en) * 1982-12-20 1984-06-19 General Electric Company Method for removing hydrogen sulfide from aqueous streams

Non-Patent Citations (30)

* Cited by examiner, † Cited by third party
Title
A. S. Michaels et al. in Membrane Processes in Industry and Biomedicine, M. Bier, ed., (Pleneum Press, 1971) p. 205. *
C. J. van Oss, in Progress in Separation and Purification, vol. 1, E. S. Perry, ed., (Interscience, 1968) p. 211. *
C. P. Bean in Membranes, G. Eisenman, ed. (Marcel Dekker, 1972) pp. 34 35. *
C. P. Bean in Membranes, G. Eisenman, ed. (Marcel Dekker, 1972) pp. 34-35.
Chemical and Engineering News, vol. 62, p. 33 (Jun. 25, 1984). *
Chemical Engineering, Oct. 17, 1983, pp. 16 17. *
Chemical Engineering, Oct. 17, 1983, pp. 16-17.
Chemical Week, Jun. 27, 1984, p. 96. *
F. L. Harris et al. in ibid. pp. 121 186. *
F. L. Harris et al. in ibid. pp. 121-186.
H. D. Spriggs and N. N. Li in Membrane Separation Processes, P. Meares, ed. (Elsevier, 1976) pp. 39 77. *
H. D. Spriggs and N. N. Li in Membrane Separation Processes, P. Meares, ed. (Elsevier, 1976) pp. 39-77.
Kan and Shuler, Biotechnology and Bioengineering, vol. 20, pp. 217 230 (1978). *
Kan and Shuler, Biotechnology and Bioengineering, vol. 20, pp. 217-230 (1978).
Kim, Presentation of AICHE Summer National Meeting, Denver, Col. (Aug. 29, 1983). *
Kimura and Walmet, Separation and Sciene and Technology, vol. 15, pp. 1115 1133 (1980). *
Kimura and Walmet, Separation and Sciene and Technology, vol. 15, pp. 1115-1133 (1980).
Kimura et al., Recent Developments in Separation Science, (CRC Press, Cleveland, Ohio, 1978) pp. 11 25. *
Kimura et al., Recent Developments in Separation Science, (CRC Press, Cleveland, Ohio, 1978) pp. 11-25.
Lee et al., A.I.Ch.E Journal, vol. 24, pp. 860 868 (Sep. 1978). *
Lee et al., A.I.Ch.E Journal, vol. 24, pp. 860-868 (Sep. 1978).
R. E. Treybal, Liquid Extraction, 2nd ed. (McGraw Hill, 1963), pp. 447 450. *
R. E. Treybal, Liquid Extraction, 2nd ed. (McGraw-Hill, 1963), pp. 447-450.
Travenol Laboratories, Inc. Travenol TMO Membrane Oxygenator product brochure (Jan. 1979). *
Webster and Shuler, Biotechnology and Bioengineering, vol. 20, pp. 1541 1556 (1978). *
Webster and Shuler, Biotechnology and Bioengineering, vol. 20, pp. 1541-1556 (1978).
Webster, American Biotechnology Laboratory, pp. 29 35 Dec. 1983. *
Webster, American Biotechnology Laboratory, pp. 29-35 Dec. 1983.
Y. Kuo and H. P. Gregor, Separation Science and Technology, vol. 18, pp. 421 440 (1983). *
Y. Kuo and H. P. Gregor, Separation Science and Technology, vol. 18, pp. 421-440 (1983).

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6214300B1 (en) 1994-12-02 2001-04-10 The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration Microencapsulation and electrostatic processing device
US5753797A (en) * 1995-04-09 1998-05-19 Cerberus Ag Photo-acoustic gas sensor and its manufacture and use
EP0771585A2 (en) 1995-11-06 1997-05-07 Hoechst Celanese Corporation Method for solvent extraction using a dual-skinned asymmetric microporous membrane
US5714072A (en) * 1995-11-06 1998-02-03 Hoechst Celanese Corporation Method for solvent extraction using a dual-skinned asymmetric microporous membrane
US20040181101A1 (en) * 2003-03-13 2004-09-16 3M Innovative Properties Company Method for obtaining ethanol
US7105089B2 (en) 2003-03-13 2006-09-12 3M Innovative Properties Company Liquid—liquid extraction system and method
US7122709B2 (en) 2003-03-13 2006-10-17 3M Innovative Properties Company Method for obtaining ethanol
US20060283800A1 (en) * 2003-03-13 2006-12-21 3M Innovative Properties Company Liquid-liquid extraction system and method
US7517455B2 (en) 2003-03-13 2009-04-14 3M Innovative Properties Company Liquid-liquid extraction system and method
EP2289611A1 (en) 2003-03-13 2011-03-02 3M Innovative Properties Co. Liquid-liquid extraction system and method
EP2292320A1 (en) 2003-03-13 2011-03-09 3M Innovative Properties Co. Liquid-liquid extraction system and method
EP2404663A1 (en) 2003-03-13 2012-01-11 3M Innovative Properties Co. Liquid-liquid extraction method

Also Published As

Publication number Publication date
CA1271428A (en) 1990-07-10
US4789468A (en) 1988-12-06

Similar Documents

Publication Publication Date Title
USRE34828E (en) Immobilized-interface solute-transfer apparatus
US4997569A (en) Immobilized-interface solute-transfer process
US4921612A (en) Asymmetrically-wettable porous membrane process
US5053132A (en) Asymmetrically-wettable porous membrane
Prasad et al. Solvent extraction with microporous hydrophilic and composite membranes
US4750918A (en) Selective-permeation gas-separation process and apparatus
AU599377B2 (en) Liquid/liquid extractions with microporous membranes
US5160627A (en) Process for making microporous membranes having gel-filled pores, and separations methods using such membranes
EP1255605B1 (en) Method of producing nitrogen enriched air
Kang et al. Ethanol production in a microporous hollow‐fiber‐based extractive fermentor with immobilized yeast
Prasad et al. Dispersion‐free solvent extraction with microporous hollow‐fiber modules
Pinnau et al. Gas permeation through composite membranes
US3457170A (en) Solvent separation process and apparatus
US6156096A (en) Gas separation using hollow fiber contained liquid membrane
US4894160A (en) Honeycomb structure for fluid filtration
CA2104969A1 (en) Rectifying dialyzer, membrane and process
JPH02187659A (en) Liquid chromatography using micro-porous hollow fiber
CN1060417A (en) Membrane drying process and system
EP0781162B1 (en) Method and system for extracting a solute from a fluid using dense gas and a porous membrane
EP0609339B1 (en) Process for removing alcohol from liquids
Lonsdale et al. Transport in composite reverse osmosis membranes
JP4295430B2 (en) Hollow fiber co-flow filtration device
US4834877A (en) Apparatus for membrane-permeation separations using segmented flow
EP0296881A2 (en) Multi-leaf permeable membrane module
US4222870A (en) Ultrafiltration apparatus and method

Legal Events

Date Code Title Description
FPAY Fee payment

Year of fee payment: 8

FPAY Fee payment

Year of fee payment: 12