GB1569182A - Hollow fibre mass transfer apparatus - Google Patents
Hollow fibre mass transfer apparatus Download PDFInfo
- Publication number
- GB1569182A GB1569182A GB44795/76A GB4479576A GB1569182A GB 1569182 A GB1569182 A GB 1569182A GB 44795/76 A GB44795/76 A GB 44795/76A GB 4479576 A GB4479576 A GB 4479576A GB 1569182 A GB1569182 A GB 1569182A
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- passageways
- fibers
- casing
- fluid
- passageway
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- 239000000835 fiber Substances 0.000 title claims description 87
- 238000012546 transfer Methods 0.000 title claims description 9
- 239000012510 hollow fiber Substances 0.000 claims description 32
- 238000004382 potting Methods 0.000 claims description 31
- 239000000203 mixture Substances 0.000 claims description 22
- 239000012530 fluid Substances 0.000 claims description 21
- 238000000502 dialysis Methods 0.000 claims description 17
- 239000007788 liquid Substances 0.000 claims description 14
- 238000000638 solvent extraction Methods 0.000 claims description 13
- 239000008280 blood Substances 0.000 claims description 10
- 210000004369 blood Anatomy 0.000 claims description 10
- 230000000694 effects Effects 0.000 claims description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 239000002250 absorbent Substances 0.000 claims description 4
- 230000002745 absorbent Effects 0.000 claims description 4
- 229920001296 polysiloxane Polymers 0.000 claims description 4
- 229920005989 resin Polymers 0.000 claims description 4
- 239000011347 resin Substances 0.000 claims description 4
- 238000007789 sealing Methods 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 3
- 208000036366 Sensation of pressure Diseases 0.000 claims description 2
- 238000004891 communication Methods 0.000 claims description 2
- 239000012535 impurity Substances 0.000 claims description 2
- 239000004615 ingredient Substances 0.000 claims description 2
- 238000002844 melting Methods 0.000 claims description 2
- 230000008018 melting Effects 0.000 claims description 2
- 238000012986 modification Methods 0.000 claims description 2
- 230000004048 modification Effects 0.000 claims description 2
- 238000006213 oxygenation reaction Methods 0.000 claims description 2
- 239000004417 polycarbonate Substances 0.000 claims description 2
- 229920005668 polycarbonate resin Polymers 0.000 claims description 2
- 229920005990 polystyrene resin Polymers 0.000 claims description 2
- 239000011148 porous material Substances 0.000 claims description 2
- 238000000926 separation method Methods 0.000 claims description 2
- 229920005992 thermoplastic resin Polymers 0.000 claims description 2
- 229920001187 thermosetting polymer Polymers 0.000 claims description 2
- 239000001993 wax Substances 0.000 claims description 2
- 238000010276 construction Methods 0.000 description 16
- 239000007789 gas Substances 0.000 description 13
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 238000003780 insertion Methods 0.000 description 5
- 230000037431 insertion Effects 0.000 description 5
- 239000004902 Softening Agent Substances 0.000 description 4
- 210000003734 kidney Anatomy 0.000 description 3
- -1 polyethylene Polymers 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 235000013869 carnauba wax Nutrition 0.000 description 2
- 239000004203 carnauba wax Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000000153 supplemental effect Effects 0.000 description 2
- 238000013022 venting Methods 0.000 description 2
- 238000003466 welding Methods 0.000 description 2
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 239000004970 Chain extender Substances 0.000 description 1
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 238000006640 acetylation reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 229920006333 epoxy cement Polymers 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229940074928 isopropyl myristate Drugs 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D63/00—Apparatus in general for separation processes using semi-permeable membranes
- B01D63/02—Hollow fibre modules
- B01D63/04—Hollow fibre modules comprising multiple hollow fibre assemblies
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D63/00—Apparatus in general for separation processes using semi-permeable membranes
- B01D63/02—Hollow fibre modules
- B01D63/031—Two or more types of hollow fibres within one bundle or within one potting or tube-sheet
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2313/00—Details relating to membrane modules or apparatus
- B01D2313/08—Flow guidance means within the module or the apparatus
- B01D2313/083—Bypass routes
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- External Artificial Organs (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
Description
(54) HOLLOW FIBER MASS TRANSFER APPARATUS
(71) We, EXTRACORPOREAL MEDICAL
SPECIALTIES, INC, a Corporation organised and existing under the laws of the State of
Pennsylvania, United States of America, located at Royal and Ross Roads, King of
Prussia, State of Pennsylvania, United States of America, do hereby declare the invention for which we pray that a Patent may be granted to us and the method by which it is to be performed, to be particularly described in and by the following statement: The present invention relates to hollow fiber mass transfer apparatus and particularly, but not exclusively, to apparatus for the dialysis of liquids such as blood.
There have been many suggestions for improving dialysis equipment especially of the artificial kidney type. A great many so-called coil-type artificial kidneys are in use in which the dialysis element is a tube many inches in diameter, but flattened and spirally wound with a spacer to separate the turns of the winding. An artificial kidney so made is relatively large in size, and there have been suggestions for smaller constructions having bundles of thousands of hollow fibers each a very narrow tube that functions as a dialysis element, but this modified construction still presents problems. An example of hollow tiber apparatus is shown in USP 3,442,002, and a fiber which has recently come into use for hollow fiber dialyzers is deacetylated cellulose acetate fiber referred to in USP 3,545,209. These fibers are generally required to be kept wet with water at all times after the de-acetylation, in order to maintain their dialytic permeability. This has led to the awkwardness of shipping and storing dialyzers based on such hollow fibers while the fibers are filled with water and with the water containing formaldehyde to keep it from developing microbial growth. Before each use it then becomes necessary to flush out all the formaldehyde.
Among the objects of the present invention is the provision of an improved hollow fiber mass transfer apparatus.
According to the present invention we provide a hollow fiber mass transfer apparatus having an elongated tubular casing containing partitioning that divides its interior into separate longitudinally extending passageways, flow directing means for receiving first fluid from an external source and directing it to flow from one casing end to the other through one of the passageways and then back to said one casing end through another of the passageways and so to and fro lengthwise through the other passageways and finally out of the casing, more than two of the passageways each having a longitudinally extending bundle of elongated semi-permeable hollow fibers extending lengthwise through it, and means connected to deliver a second fluid from an inlet to the fiber ends of each of such bundles at the same end of the casing and to receive the second fluid from the other ends of the hollow fibers for delivery to an outlet, the passageways having bundles of fibers being clustered around a common centreline. The present invention is more fully explained in the following descriptions of several of its exemplifications, reference being made to the accompanying drawings in which:
Figure 1 is an elevational view partly in section and partly broken away, of one embodiment of an apparatus in accordance with the present invention, in the form of a hollow fiber dialyze, Figures 2, 3 and 4 are sectional views of the construction of Figure 1, taken along the lines 2-2, 3-3 and 44, respectively;
Figure 5 is a view similar to Figure 1 of a modified hollow fiber dialyzer;
Figures 6, 7 and 8 are sectional views of the construction of Figure 5 taken along the lines 6-6, 7-7 and 8-8, respectively;
Figures 9, 10, 11 and 12 are views similar to Figures 1, 2, 3 and 4 of a further modified hollow fiber dialyzer; and
Figure 13 is a sectional view of a cap suitable for use with the construction of Figure 9.
In each of the embodiments illustrated, the hollow fiber dialyzer has an elongated tubular casing with ends of larger bore than its central portion, the central portion containing longitudinally-extending partitioning that divides its interior into a plurality of generally parallel passageways, the casing ends containing dialyzate flow manifolding and directing means for receiving dialyzate from a supply thereof, directing it from one casing end to the other through one of the passageways, and so to and fro through the successive passageways, finally directing the dialyzate out through a discharge opening, bundles of parallel hollow dialysis fibers being crowded into at least all of the passageways in which the directing means directs dialyzate flow in one of the two flow directions.
The following examples illustrate very desirable manners of preparing hollow fiber dialyzers.
EXAMPLE I
A dialysis casing such as shown at 10 in
Figure 1 and molded or cemented together from polycarbonate or polystyrene resin, is first provided. This casing has an over-all length of about 7'A inches with its intermediate portion 12 having an internal diameter of 13/s inches, each end 14, 16 being of enlarged bore having an internal diameter of about 1 171a inches. The tubular length of the interior of the casing is divided into three individual passageways 21, 22, 23 by an axial web 26 of three flanges, 31,32 and 33. An inlet tube 36 opens into enlarged end 14, and a discharge tube 38 leads out from end 16.
Web 26 has flow control means at each end 14, 16 arranged so that fluid entering inlet 36 flows upwardly through passageway 21 from end 14 to end 16, then at end 16 moves from the top of passageway 21 to the top of passageway 22, then downwardly through passageway 22 to lower end 14 where it then transfers to the bottom of passageway 23 along which it moves upwardly to end 16 for discharge through outlet 38. To effect this flow control, flange 31 is arranged as a barrier seal against the outer wall of the casing throughout the length of lower end 14 as well as throughout the length of the intermediate portion 12, but not at the upper end 16. Instead at that upper end flange 31 is cut out as shown at 40 to provide a flow-through space 41 that thus opens between the upper ends of passageways 21 and 22.
Flange 32 is similarly shaped in an opposite sense so that at its lower portion it provides an edge 50 spaced from the lowest point of casing end 14 to provide a flow-through space 51 between the lower ends of passageways 22 and 23.
A batch of hollow cuprammonium regenerated cellulose fibers having a wall thickness of about 12 microns plus or minus 2 microns and an internal diameter of about 200 microns plus or minus 50 microns is unspooled, preferably from a plurality of spools in parallel strands, cut to a length of about 9 inches and carefully cleaned. As generally supplied these fibers are made by extruding cuprammonium cellulose solution through an annular die into a regenerating bath while introducing a waterimmiscible liquid into the bore of the hollow extrudate. A typical water-insoluble liquid is isopropylmyristate. After regeneration is completed careful washing with isopropanol removes such liquid. The interiors of the fibers can then be wet with a softening agent such as gylcerine, preferably leaving about 5% of the softening agent by weight of the clean fiber. This softening is not essential but helps guard the fibers against breakage or damage during subsequent handling, and does not detract from the effectiveness by which the fibers are sealed into the casing 10.
A bundle of two to three thousand fibers so prepared is then inserted into one of the passageways 21, 22, 23, and additional bundles in each of the remaining passageways. This insertion can be expedited by first sliding over the bundle a tapered sleeve of polyethylene, then introducing the filled sleeve, narrow end first, into one of the passageways, and finally pulling the sleeve off the introduced bundle.
At the narrow end of the taper the fibers are arranged to project from the sleeve so they can be gripped to help pull the sleeve off the other ends of the fibers.
When all the passageways are filled with fibers, the potting can be started. At each end of the casing each bundle of fibers projects a short distance. Each of these projecting ends is dipped in melted carnauba wax which is then permitted to solidify after the carnauba wax has penetrated a very short distance into all of the individual fibers. The casing is then clamped longitudinally between potting heads connected to a potting compound container as illustrated in Figure 1 9 of U.S. Patent 3,442,002, and centrifuged as also indicated in that patent while the uncured liquid freshly mixed potting mixture is poured into the potting compound container. This mixture can be a polyurethane prepolymer resin with a chain extender, or an epoxy cement mixture as described in U.S. Patent 3,442,002 or a hardenable polysiloxane liquid or other settable resin.
When a hardenable polysiloxane liquid with a curing agent such as chlorplatinic acid is used, the centrifuging is conducted at about 350g while the mixture is heated, and after about 1M2 hour at 150"F. the potting mixture is cured to the point that it no longer flows.
The potting heads are then unclamped and removed, and the curing completed by holding the dialyzer in an air oven at 1 500F for two hours. After that the potting mixture is a cleanly cutting solid and a sharp metal blade is used to cut the potting mixture flush with the open ends 14, 16 of the casing. This leaves the construction as illustrated in Figure 1, the potting composition being shown at 56 and 57.
Covers 61, 62 each equipped with a flow connection 64, 65 are then fitted to the casing ends 14, 16 as by welding or cementing, although they can also be threaded in place if desired. The construction is then complete and only needs a flushing through to remove the water-soluble softening agent from the inside of the hollow fibers before it is placed in service. The dialyzers can be stored either before or after washing out the softening agent, without significantly affecting their dialysis properties.
When the dialyzer is used it is generally held with end 16 up, a source of dialyzate is connected to inlet 36, discharge 38 is connected to waste, and a supply of blood to be dialyzed connected to inlet 65 with a blood return to outlet 64. In use bubbles of air or other gases can form in the dialyzate and tend to rise toward the upper end 16 of the dialyzer. To keep those bubbles from becoming trapped at the upper ends of passageways 21 and 22 and collecting there in an amount that could interfere with the dialysis, a small bleed 59 is shown as provided at the upper end of web flange 32.
For a flange with a wall thickness of l/l6 inch a round opening as little as 1S millimeter in diameter will enable the gas trapped at the above-mentioned ends to readily make its way into the upper end of passageway 23 and out through discharge opening 38, without significantly reducing the effectiveness of the dialysis. The gas vent can even be made slightly smaller as for example 0.3mm. in diameter.
The optimum width of the vent is related to the thickness of the wall through which it penetrates. For wall thicknesses greater than l/l6 inch the vent width is preferably a little larger than X millimeter.
A feature of the dialyzer construction of
Figure 1 is that such dialyzers are readily manufactured with more uniform dialysis effectiveness than corresponding dialyzers in which there is no partitioning and web 26 is completly omitted. Notwithstanding the enlarged ends 14,16 which serve as dialyzate manifolds that bring the dialyzate into direct contact with the outer layers of fibers in the fiber bundles, the dialyzate has a tendency to make its way through one end of the dialyzer to the other through the easiest path and thus find and establish a channel, even when the fibers are fairly well packed in place. Such channelling greatly-reduces the effectiveness of the dialysis particularly through the walls of those fibers that are some distance laterally spaced from the channel. When this happens with a dialyzer containing only a single dialyzate passageway, its efficiency becomes so poor that it generally has to be discharged.
Such channelling is more likely to take place as the wall thickness of the hollow fibers diminishes and as the fiber diameter decreases; these cause the fibers to be more flexible so that it is easier for the dialyzate to create a channel by deflecting the fibers. Wall thicknesses of about 5 to about 20 microns are suitable for effective use and thicknesses of from about 10 to about 15 microns are preferred. Fibers with internal passageways not over about 500 microns wide, preferably ranging from about 100 to about 300 microns in width, are very effective. Cuprammonium regenerated hollow fibers of this type are relatively stiff, particularly when dry, and are accordingly very easy to handle in the assembling of a bundle for insertion in a dialyzer, and in the insertion itself.
In the construction of Figure 1 a channelling-induced drop in efficiency of passageway 21 can also occur, but when that happens the dialyzate emerging from passageway 21 is less loaded with contaminants so that it becomes more effective in its subsequent passage through passageways 22 and 23.
In addition each of the passageways 21, 22 and 23 is narrower than it would be without the web 26, and channelling becomes less likely in narrower passageways. Also the total length of fibers contacted by the dialyzate in the construction of Figure 1 is three times the length contacted if web 26 were omitted, and the efficiency loss through channelling diminishes as such length increases.
Because of the more reproducible greater efficiencies of the construction of Figure 1, dialyzers having an operating length between potting seals 56, 57, of only about 1 5 centimeters can be readily manufactured with the desired high qualities. This small bulk is particularly desirable, although in general overall lengths of from about 6 to about 12 inches can be attractive for hospital use.
EXAMPLE 2
In the dialyzer 110 of Figures 5 to 8, there are three parallel dialyzer passageways along the lines of Figure 1 but the flow of dialyzate is arranged so that throughout its fibercontacting path it moves on the outside of the individual fibers in a direction countercurrent to the flow of blood or other medium being dialyzed within the fibers..
As in the construction of Figure 1, dialyzer 110 has a central tubular section 112 with enlarged ends 114, 116 and with a partitioning web 126 inserted or molded in section 112.
Web 126 has flanges 131,132,133 similar to the three flanges of web 26, and in addition also has two supplemental flanges 134, 135 that define supplemental passageways 1 24, 125.
The bundles of hollow fibers are contained in passageways 121,122,123; passageways 124, 125 being unfilled so that they provide paths for the dialyzate to flow while out of contact with the fibers.
The flow of dialyzate is controlled by appropriate shaping of the web flanges in the construction of Figure 5 so that it enters and flows upwardly first through passage 121 then downwardly through passage 124 then back upwardly through passageway 122 returning this time to the bottom via passageway 125, and finally completing the dialysis by an upward travel through passageway 123 and discharge at outlet 138. For this result, the upper ends of webs 134 and 135 are spaced from the inside wall of casing end 116 and the lower ends of webs 131 and 132 are spaced from the inside surface of casing end 114, as more clearly illustrated in Figures 7 and 8.
No gas vent is provided in the construction of Figure 5 inasmuch as the dialyzate flow rate is fairly high in the very narrow return passageways 124, 125. Thus a flow rate of only about one foot a second is generally sufficient to sweep out gas bubbles that tend to form. For slower flow rates, as for example when the dialyzate is discarded after a single passage through the dialyzer and is not recirculated from outlet 138 back to inlet 136, gas venting can be provided in the construction of Figure 5.
Gas venting can be eliminated where the dialyzate is treated to reduce gas evolution, as for example by boiling it under reduced pressure before it is introduced into the dialyzer.
This removes almost all of the dissolved gases, and the maintenance of some pressure on the dialyzate as it is impelled through the dialyzer acts as an additional preventive to gas evolution.
The dialyzer casings need not L circular in cross-section but can be oval, rectangular or triangular if desired, both in their external shape as well as in the shape of the passageways. Similarly, they do not have to be perfectly linear in longitudinal direction.
EXAMPLE 3
Figures 9 through 13 illustrate a dialyzer 210 which is generally triangular in crosssection, particularly at its ends 214, 216. Those ends each have a mounting rib 217 which helps in positioning end connector covers 262.
Moreover each rib 217 can be provided with a ridge 219 which need only be about 15 to about 20 mils high that helps in welding the cover in place as by sonic or ultrasonic vibration of the mounted cover against that ridge.
Upon vibration in this manner the ridge and the ridge-engaging portion of the cover fuse as a result of the frictional heating effects of the vibration between them, and weld together making a very effective fluid-tight seal.
The construction and operation of Figures 9 through 13 generally corresponds to that of
Figures 5 through 8, and similar portions such as partitioning web 226, passageways 221, 222 and 223 for receiving the hollow fibers, passageways 224 and 225 for dialyzate return, and inter-passage spacings 241, are similarly numbered. However, to better seal the blood or other dialyzand away from undesired crevices and the like, covers 262 are each provided with an internal sealing lip 263 shaped to engage the potting seal 257 outside the fibercontaining zone. The dialyzand is thus kept from penetrating into the crevice 265 between the internal surface of the cover and external surface of the casing wall.
To further help with such sealing, the potting seal 257 can be arranged to project out a short distance 267, such as 1(8 inch, beyond the casing end.
The fiher bundles can be inserted in the dialyzer passageways without the help of a sleeve, particularly if the walls of a casing end provide a gradual taper from their large internal bore down to the smaller bore of central portion 12 or 112. Alternatively the bundles can be sleeved and the sleeves left in the dialyzer in position around the bundles. This alternative is particularly desirable when the sleeves are of relatively thin wall section, i.e.
about 3 mils, so that they do not occupy much room.
The insertion of the fiber bundles is also made easier if this is done when the casings are hot. The heat expands the casing and thus provides a little more room for more readily sliding the bundles into place, after which the casing cools down and tightly encloses the fibers, thus making for added efficiency.
Instead of an elongated sleeve to help the fiber insertion, a single narrow length of plastic or even wire can be looped around a fiber bundle adjacent one end, and tied or crimped against the fibers so as to provide a tail for the bundle. The bundle can then be pulled througl a passageway by first passing the tail through the passageway and then pulling on the tail.
It is generally desirable to clean the hollow fibers for the dialysis as by washing or rinsing them with a readily volatilizable solvent, particularly where the bore in the fibers contain a liquid which should not contact the dialyzand or dialyzate.
The partitioning can even be more subdivided than is shown in the drawings so as to provide 4 or 5 parallel dialysis passageways, but the use of more partitions takes away some of the space for fibers so that the bulk o the casing has to be increased to maintain the dialyzing effectiveness.
The partitioning simplifies the mechanical handling in the manufacture of the dialyzer.
The reduced width of the individual passageways, e.g. one to three centimeters, as compared to an unpartitioned dialyzer, reduces the number of fibers per passageway and thus simplifies the preparation of the individual bundles. By way of illustration, the task of preparing a 6000-fiber bundle for an unpartitioned dialyzer is more complex than that of preparing three 2000-fiber bundles for use in t the dialyzer of Figure 1 or Figure 5 or Figure
9.
The fiber-containing passageways can also
be double tapered as illustrated at 211 in
Figure 9 so that they provide a constriction in
their central portions. Such a constriction of
about X to 1 millimeter helps grip the fibers
and keep them from being deflected by the
flow around them, thus reducing the tendency
to channelling.
The different compartments of the des
cribed dialyzers need not be used for the same
function. One of the compartments can for
example be used to hold an absorbent such as
activated charcoal or the like, instead of fibers,
so as to absorb impurities or other undesirable
ingredients in the dialyzand. Different kinds
of fibers can be used in different passageways
to obtain different dialysis effects on the
dialyzand as it passes through the dialyzer.
Indeed some of the passageways, such as
passageway 124, can be filled with absorbent
for the purpose of treating the dialyzate as it
moves through the dialyzer and better condi
tion the dialyzate for its passage through the
remaining fiber-containing passageways.
The potting of the fiber ends can be accom
plished with techniques other than that des
cribed above. Thus the preliminary dip of the
fibers to plug their bores can be into melted
resin-modified waxes or thermoplastic resins
or compositions that harden to form thermo
setting resins. The potting mixture itself can
for example be used as a preliminary dip of
shallow depth, followed by deeper potting.
Also, by maintaining slightly higher pressure
in unplugged fiber bores as against the pres
sure over the potting mixture into which the
unplugged fiber ends are dipped, the potting
mixture is kept at a low level within those
bores and the preliminary dip to plug those
bores can be completely eliminated. The bores
can alternatively be sealed by melting the fiber
ends when they are of fusible nature, and in
this way make a prior dip unnecessary.
While centrifugal force applied to the liquid
potting mixture helps to ensure that such mix
ture thoroughly impregnates all crevices and
pores around and between the fibers and in
this way ensures thorough sealing of the dialy
zate chamber from the dialyzand, gas pressure
applied over the liquid potting composition
during potting, has a similar effect. One end
of a fiber bundle can accordingly be potted
at a time, without the need for the centrifugal
potting apparatus.
Also, the covers 61, 62 can be arranged to
snap on over the potted ends of the dialyzer,
as shown in Figure 5 at 161, 162 for example.
Such covers can be relatively flexible and the
potted ends they snap over can be fitted with
ridges as at 163 to help lock the snap on covers
in place.
The apparatus of the present invention is
also suitable for use in osmosis or in gas separation, with appropriate types of fiber, or in gas treatment of liquids as in the oxygenation of blood where silicone fibers are preferred.
Obviously many modifications and variations of the present invention are possible in the light of the above teachings. It is, therefore to be understood that within the scope of the appended claims the invention may be practised otherwise than as specifically described.
WHAT WE CLAIM IS:- 1. A hollow fiber mass transfer apparatus having an elongated tubular casing containing partitioning that divides its interior into separate longitudinally-extending passageways, flow directing means for receiving first fluid from an external source and directing it to flow from one casing end to the other through one of the passageways and then back to said one casing end through another of the passageways and so to and fro lengthwise through the other passageways and finally out of the casing, more than two of the passageways each having a longitudinally-extending bundle of elongated semi-permeable hollow fibers extending lengthwise through it, and means connected to deliver a second fluid from an inlet to the fiber ends of each of such bundles at the same end of the casing and to receive the second fluid from the other ends of the hollow fibers for delivery to an outlet, the passageways having bundles of fibers being clustered around a common centreline.
2. Apparatus as claimed in Claim I, where- in some of the passageways do not contain hollow fibers and are located adjacent the lateral periphery of the elongated casing.
3. Apparatus according to Claim 1 or 2 wherein the passageways having bundles of fibers are of relatively wide cross-section, and the passageways which do not contain the hollow fibers are of relatively narrow and circular cross-section.
4. Apparatus as claimed in Claim 3, whereii the passageways having bundles of fibers are generally circular in cross-section throughout their length between the first fluid entrance and exit ends.
5. Apparatus as claimed in any preceding
Claim wherein there are three passageways having the bundles of fibers and two passageways which do not contain fibers, and the three passageways having the bundles of fibers are arranged in closely-packed triangular relationship.
6. Apparatus according to Claim 5, wherein the tubular casing is integrally molded to contain longitudinal partitioning that subdivides it into five longitudinally extending side-byside passageways, three of them being of wider cross-section than the other two, the three wider passageways being about equal in size, the partitioning containing inter-passage communication openings that permit fluid introduced into one of the wider passageways near one end of the casing to move through that
**WARNING** end of DESC field may overlap start of CLMS **.
Claims (12)
1. A hollow fiber mass transfer apparatus having an elongated tubular casing containing partitioning that divides its interior into separate longitudinally-extending passageways, flow directing means for receiving first fluid from an external source and directing it to flow from one casing end to the other through one of the passageways and then back to said one casing end through another of the passageways and so to and fro lengthwise through the other passageways and finally out of the casing, more than two of the passageways each having a longitudinally-extending bundle of elongated semi-permeable hollow fibers extending lengthwise through it, and means connected to deliver a second fluid from an inlet to the fiber ends of each of such bundles at the same end of the casing and to receive the second fluid from the other ends of the hollow fibers for delivery to an outlet, the passageways having bundles of fibers being clustered around a common centreline.
2. Apparatus as claimed in Claim I, where- in some of the passageways do not contain hollow fibers and are located adjacent the lateral periphery of the elongated casing.
3. Apparatus according to Claim 1 or 2 wherein the passageways having bundles of fibers are of relatively wide cross-section, and the passageways which do not contain the hollow fibers are of relatively narrow and circular cross-section.
4. Apparatus as claimed in Claim 3, whereii the passageways having bundles of fibers are generally circular in cross-section throughout their length between the first fluid entrance and exit ends.
5. Apparatus as claimed in any preceding
Claim wherein there are three passageways having the bundles of fibers and two passageways which do not contain fibers, and the three passageways having the bundles of fibers are arranged in closely-packed triangular relationship.
6. Apparatus according to Claim 5, wherein the tubular casing is integrally molded to contain longitudinal partitioning that subdivides it into five longitudinally extending side-byside passageways, three of them being of wider cross-section than the other two, the three wider passageways being about equal in size, the partitioning containing inter-passage communication openings that permit fluid introduced into one of the wider passageways near one end of the casing to move through that
passageway to a location near the other end of the casing, the move from there into one of the smaller passageways and back through that smaller passageway to a location near said one end, from there move into a second wider passageway and through that passageway to a location near said other end, from there into the second smaller passageway and through that passageway back to a location near said one end, from there into the third wider passageway and through that passageway to a location near said other end, wherein the five passageways are clustered about a common longitudinal centreline with the three wider passageways arranged in closely-packed triangular relationship, and the two smaller passageways are each circular in cross-section.
7. Apparatus according to any preceding
Claim wherein each of the passageways having a bundle of fibers therein has the fibers packed in it, and the first fluid flow directing means further includes manifolding of enlarged crosssection to direct the first fluid into contact with the outer layers of fibers in each of said bundles as the first fluid enters each such passageway whereby to reduce undesirable channelling of the first fluid.
8. Apparatus as claimed in Claim 6, wherein the manifolding of enlarged cross-section is defined by laterally enlarged casing ends.
9. Apparatus according to any preceding
Claim wherein at one end of the casing, the flow directing means contains a gas bypass connected between successive passageways to permit gas bubbles trapped at that end, when the apparatus is operated with that end up, to be discharged out of the casing without having to be carried by the first fluid to the other end.
10. Apparatus according to any preceding
Claim wherein the casing is molded of polycarbonate or polystyrene resin.
11. Apparatus as claimed in any one of
Claims 1 to 10 in the form of a blood dialyzer, wherein the hollow fibers are blood dialysis fibers, the second fluid is blood and the first fluid is a dialyzate.
12. A hollow fiber mass transfer apparatus substantially as hereinbefore described with reference to Figures 1 to 4, Figures 5 to 8, or
Figures 9 to 13 of the accompanying drawings.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US62908275A | 1975-11-05 | 1975-11-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1569182A true GB1569182A (en) | 1980-06-11 |
Family
ID=24521502
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB44795/76A Expired GB1569182A (en) | 1975-11-05 | 1976-10-28 | Hollow fibre mass transfer apparatus |
Country Status (12)
Country | Link |
---|---|
JP (2) | JPS5258079A (en) |
AR (1) | AR215452A1 (en) |
BE (1) | BE847969A (en) |
BR (1) | BR7607355A (en) |
CA (3) | CA1100887A (en) |
DE (1) | DE2650588A1 (en) |
FR (1) | FR2330429A1 (en) |
GB (1) | GB1569182A (en) |
IT (1) | IT1063433B (en) |
MX (1) | MX143979A (en) |
NL (1) | NL165058C (en) |
SE (2) | SE7611942L (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2499902A1 (en) * | 1981-02-13 | 1982-08-20 | Akzo Nv | HOLLOW FIBER MODULE, AND METHOD AND DEVICE FOR MANUFACTURING THE SAME |
EP2145674A1 (en) * | 2000-12-18 | 2010-01-20 | Mitsubishi Rayon Co., Ltd. | hollow fiber membrane module and method of manufacturing the same |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE393535B (en) * | 1975-09-11 | 1977-05-16 | Gambro Ab | DEVICE FOR DIFFUSION OF THE SUBJECT BETWEEN TWO FLUIDES VIA SEMIPERMEABLE MEMBRANE |
JPS5313594A (en) * | 1976-07-23 | 1978-02-07 | Nippon Zeon Co | Method of producing hollow fiber substance moving device |
JPS5753564Y2 (en) * | 1977-06-01 | 1982-11-19 | ||
JPS5622911Y2 (en) * | 1977-08-27 | 1981-05-29 | ||
SE422000B (en) * | 1977-10-17 | 1982-02-15 | Gambro Dialysatoren | DEVICE FOR DIFFUSION AND / OR FILTRATION OF THE SUBSTANCE BETWEEN TWO FLUIDS THROUGH SEMIPERMEABLE MEMBRANE, WHICH DEVICE INCLUDES A STACK OF CAMERA IMAGE FRAMES CONTAINING THE SENSOR |
JPS5492580A (en) * | 1977-12-29 | 1979-07-21 | Nippon Zeon Co Ltd | Hollow fiber type material transferring apparatus |
CA1132914A (en) * | 1978-03-20 | 1982-10-05 | Bert S. Bodnar | Method of potting the ends of a bundle of hollow fibers positioned in a casing |
JPS55114A (en) * | 1978-06-15 | 1980-01-05 | Honda Motor Co Ltd | Dialyzer device in artificial kidney device |
SE458826B (en) * | 1982-08-23 | 1989-05-16 | Albany Int Corp | Separator |
JPS60232207A (en) * | 1984-05-01 | 1985-11-18 | Asahi Chem Ind Co Ltd | Method for assembling hollow yarn type filter |
JPS6163240U (en) * | 1984-09-29 | 1986-04-28 | ||
JP4955855B2 (en) * | 2001-01-05 | 2012-06-20 | 三菱レイヨン株式会社 | Hollow fiber membrane module and manufacturing method thereof |
DE10106722B4 (en) * | 2001-02-14 | 2008-11-06 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Special hollow fiber membrane module for use in heavily fouled processes and its production |
JP5216916B2 (en) * | 2008-07-15 | 2013-06-19 | ミリメディカル・リミテッド・ライアビリティ・カンパニー | Double fiber bundle dialyzer |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3728256A (en) * | 1971-06-22 | 1973-04-17 | Abcor Inc | Crossflow capillary dialyzer |
FR2231421B1 (en) * | 1973-05-30 | 1976-05-07 | Rhone Poulenc Ind | |
JPS50131395A (en) * | 1974-04-04 | 1975-10-17 | ||
SE393535B (en) * | 1975-09-11 | 1977-05-16 | Gambro Ab | DEVICE FOR DIFFUSION OF THE SUBJECT BETWEEN TWO FLUIDES VIA SEMIPERMEABLE MEMBRANE |
-
1976
- 1976-10-27 SE SE7611942A patent/SE7611942L/en unknown
- 1976-10-28 GB GB44795/76A patent/GB1569182A/en not_active Expired
- 1976-11-03 BR BR7607355A patent/BR7607355A/en unknown
- 1976-11-03 IT IT29002/76A patent/IT1063433B/en active
- 1976-11-03 MX MX166882A patent/MX143979A/en unknown
- 1976-11-03 CA CA264,841A patent/CA1100887A/en not_active Expired
- 1976-11-03 FR FR7633098A patent/FR2330429A1/en active Granted
- 1976-11-04 AR AR265353A patent/AR215452A1/en active
- 1976-11-04 DE DE19762650588 patent/DE2650588A1/en not_active Ceased
- 1976-11-04 JP JP51131810A patent/JPS5258079A/en active Granted
- 1976-11-04 BE BE172064A patent/BE847969A/en not_active IP Right Cessation
- 1976-11-05 NL NL7612323.A patent/NL165058C/en not_active IP Right Cessation
-
1980
- 1980-09-08 CA CA359,854A patent/CA1106770A/en not_active Expired
- 1980-09-08 CA CA359,855A patent/CA1106771A/en not_active Expired
- 1980-10-17 JP JP14452080A patent/JPS5697458A/en active Pending
-
1981
- 1981-02-06 SE SE8100863A patent/SE434120B/en unknown
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2499902A1 (en) * | 1981-02-13 | 1982-08-20 | Akzo Nv | HOLLOW FIBER MODULE, AND METHOD AND DEVICE FOR MANUFACTURING THE SAME |
DE3105192A1 (en) * | 1981-02-13 | 1982-09-09 | Akzo Gmbh, 5600 Wuppertal | HOLLOW FIBER MODULE AND METHOD AND DEVICE FOR ITS PRODUCTION |
EP2145674A1 (en) * | 2000-12-18 | 2010-01-20 | Mitsubishi Rayon Co., Ltd. | hollow fiber membrane module and method of manufacturing the same |
US7749381B2 (en) | 2000-12-18 | 2010-07-06 | Mitsubishi Rayon, Co., Ltd. | Hollow fiber membrane module, and a manufacturing method therefor, and housing for hollow fiber membrane module |
CN101732995B (en) * | 2000-12-18 | 2013-04-03 | 三菱丽阳株式会社 | Hollow fiber membrane module, method of manufacturing the hollow fiber membrane module, and housing for hollow fiber membrane module |
Also Published As
Publication number | Publication date |
---|---|
SE7611942L (en) | 1977-05-06 |
JPS5258079A (en) | 1977-05-13 |
CA1106770A (en) | 1981-08-11 |
SE434120B (en) | 1984-07-09 |
NL7612323A (en) | 1977-05-09 |
CA1100887A (en) | 1981-05-12 |
BR7607355A (en) | 1977-09-20 |
NL165058C (en) | 1981-03-16 |
CA1106771A (en) | 1981-08-11 |
BE847969A (en) | 1977-05-04 |
AR215452A1 (en) | 1979-10-15 |
NL165058B (en) | 1980-10-15 |
IT1063433B (en) | 1985-02-11 |
MX143979A (en) | 1981-08-14 |
JPS5616687B2 (en) | 1981-04-17 |
JPS5697458A (en) | 1981-08-06 |
FR2330429A1 (en) | 1977-06-03 |
DE2650588A1 (en) | 1977-05-18 |
SE8100863L (en) | 1981-02-06 |
FR2330429B1 (en) | 1983-02-25 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed [section 19, patents act 1949] | ||
PCNP | Patent ceased through non-payment of renewal fee |