CA1101785A - Radial compression of packed beds - Google Patents
Radial compression of packed bedsInfo
- Publication number
- CA1101785A CA1101785A CA266,277A CA266277A CA1101785A CA 1101785 A CA1101785 A CA 1101785A CA 266277 A CA266277 A CA 266277A CA 1101785 A CA1101785 A CA 1101785A
- Authority
- CA
- Canada
- Prior art keywords
- chamber
- mass
- column
- packing
- wall
- 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
Links
- 238000007906 compression Methods 0.000 title claims description 45
- 230000006835 compression Effects 0.000 title claims description 44
- 238000012856 packing Methods 0.000 claims abstract description 86
- 238000000034 method Methods 0.000 claims abstract description 54
- 230000008569 process Effects 0.000 claims abstract description 29
- 239000002245 particle Substances 0.000 claims description 33
- 239000000463 material Substances 0.000 claims description 28
- 239000011800 void material Substances 0.000 claims description 20
- 239000012530 fluid Substances 0.000 claims description 14
- -1 poly(tetrafluoroethylene) Polymers 0.000 claims description 14
- 229920000642 polymer Polymers 0.000 claims description 14
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims description 9
- 238000000576 coating method Methods 0.000 claims description 8
- 239000011248 coating agent Substances 0.000 claims description 7
- 238000004811 liquid chromatography Methods 0.000 claims description 7
- 239000004698 Polyethylene Substances 0.000 claims description 6
- 238000004587 chromatography analysis Methods 0.000 claims description 6
- 229920000573 polyethylene Polymers 0.000 claims description 6
- 239000004810 polytetrafluoroethylene Substances 0.000 claims description 6
- 230000005526 G1 to G0 transition Effects 0.000 claims description 4
- 239000004033 plastic Substances 0.000 claims description 4
- 229920003023 plastic Polymers 0.000 claims description 4
- 230000007423 decrease Effects 0.000 claims description 3
- 239000011888 foil Substances 0.000 claims description 3
- 238000001816 cooling Methods 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 229910001220 stainless steel Inorganic materials 0.000 claims description 2
- 239000010935 stainless steel Substances 0.000 claims description 2
- 210000000188 diaphragm Anatomy 0.000 claims 7
- 239000011368 organic material Substances 0.000 claims 2
- 239000002861 polymer material Substances 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 239000007769 metal material Substances 0.000 claims 1
- 229920000620 organic polymer Polymers 0.000 claims 1
- 229920000136 polysorbate Polymers 0.000 claims 1
- 238000000638 solvent extraction Methods 0.000 claims 1
- 239000007788 liquid Substances 0.000 abstract description 11
- 230000008901 benefit Effects 0.000 description 11
- 230000000694 effects Effects 0.000 description 8
- 239000007789 gas Substances 0.000 description 8
- 230000005465 channeling Effects 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 238000009826 distribution Methods 0.000 description 6
- 239000002002 slurry Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 5
- 229910000831 Steel Inorganic materials 0.000 description 4
- 238000010276 construction Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- 239000010959 steel Substances 0.000 description 4
- 239000004809 Teflon Substances 0.000 description 3
- 229920006362 Teflon® Polymers 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000013598 vector Substances 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 238000010420 art technique Methods 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000005457 optimization Methods 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000010079 rubber tapping Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229910000619 316 stainless steel Inorganic materials 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920005654 Sephadex Polymers 0.000 description 1
- 239000012507 Sephadex™ Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000002238 attenuated effect Effects 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000012612 commercial material Substances 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000007596 consolidation process Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000011243 crosslinked material Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 238000001962 electrophoresis Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 229910000743 fusible alloy Inorganic materials 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 238000000506 liquid--solid chromatography Methods 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- 239000004701 medium-density polyethylene Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011860 particles by size Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000006223 plastic coating Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 230000003252 repetitive effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
- G01N30/02—Column chromatography
- G01N30/50—Conditioning of the sorbent material or stationary liquid
- G01N30/56—Packing methods or coating methods
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
- G01N30/02—Column chromatography
- G01N30/50—Conditioning of the sorbent material or stationary liquid
- G01N30/52—Physical parameters
- G01N2030/522—Physical parameters pressure
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
- G01N30/02—Column chromatography
- G01N30/60—Construction of the column
- G01N30/6052—Construction of the column body
- G01N30/6065—Construction of the column body with varying cross section
Landscapes
- Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Treatment Of Liquids With Adsorbents In General (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
Abstract of the Invention Improved liquid chromatographic apparatus and an improved process for making and utilizing a chromatographic column. By providing means to exert radial pressure on the column packing, the packing efficiency of the column is increased and is more reproducible, and greater uniformity can be achieved in column performance both among packed columns of the same kind and during the useful life of a given packed column.
Description
Background of the Invention Liquid chromatography is a process utilized in both preparative and analytical chemistry. Essentially, the process comprises a stationary phase interacting with a mobile phase. Typically, the stationary phase is a surface-active powder suchas silica, alumina, or an inert size-separating material like a gel-permeation chromatography packing, or the like. This powder is contained in a chromato-graphic column. A mobile phase, generally consisting of a carrier fluid and a sample of a chemical to be identified, analyzed, or purified, is passed through the column. A
typical utility of the process is to identify various chemical components in an unknown sample. This identification is made by (1) using an immobile phase which differentially retards the progress of different components of the sample through the column so that the components are separated and leave the column at different times and (2) continuously analyzing the effluent of the column over a period of time.
The separation ls achieved when one component of the sample has more affinity for the stationary phase than does another component. Also, the separation may be achieved by an exclusion process based on the difference in sizes between molecules, e.g., by gel-permeation chromatography processes. The invention to be described below is related to achieving better and more dependable identity of the sample components by improving the efficiency of the process in such a way as to provide better resolution of the sample.
In order to achieve separation of sample components which are very close to each other in chemical and physical .' 7~5 properties, highly sophisticated procedures have been developed in the many processing techniques associated with liquid chromatography. Special pumps and valves have been developed for presenting sample to the inlet of the chromatographic columns with as much integrity as is possible to avoid building into the process an initial and inherent dispersal of the sample which dispersal would tend to reduce the resolution capabilities of the chromatographic packing within the column.
Moreover, much work has been done to provide flow-distributing devices at the inlet of the column to assure the even place-ment of the sample across the column's cross-sectional area.
Also, a great deal of technical effort has provided improved chromatographic packings and highly-sophisticated analytical apparatus for measuring various properties of the liquid effluent leaving the column.
Despite such work as has been described above, it has remained a problem to achieve a unifo~m packing of the chromatographic material into a column. Many techniques have been suggested including vibration (See U.S. Patent 20 3,300,849): All of these techniques require careful control if segregation of particles by size is to be avoided and -uniformly packed columns are to be obtained. Even after the column is filled, problems exist in maintaining the filling in proper condition during transportation and operation of the packed columns. (See patent 3,349,920 to Waters) In general, the most commonly used practice of filling a high-performance column has been a costly method including slurrying the packing and passing the slurry into the column; thereby, in effect, using the column itself as a form for placing a "filter cake" of chromatographic X' packing therein. Even this costly, time-consuming method of column manufacture is not without problems caused by shifting of the packing during shipment when it can be subjected to various vibration and other transient, non-predictable physical abuse. This tends to cause voids in the column and such voids can wholly destroy a column's operating character-istics for many separations. Such defects in stainless steel columns are not usually detectable until a standard sample is measured as a control. Indeed, suppliers of quality chromatographic columns, until this day, have pre-tested individually each column before shipment to the customer to assure that the packing is properly placed in the column.
Of course, this "certifying procedure" provides no protection against the hazards encountered during shipment or during use by the customer. -~
A number of solutions have been suggested for holding the packing "in-place". Some of these, like the aforementioned vibration technique and slurrying technique, emphasize a maximum effort to put a conventional packing into the column in such a way as to have it assume a stable position. Other techniques such as those described in U.S.
patent 3,808,125 to Good use rather complex or expensive procedures for fastenin~ the packing to the column wall.
None of these attempts by the prior art have been dependably successful in achieving any of an excellent perform-ance, a column-to-column consistency in separating character- -istics, or a desired degree of stability of performance over a period of time for a single column, at a cost which can make the apparatus available to the broadest spectrum of chromatographers.
s Although the foregoing description of problems relating to chromatographic columns has been largely devoted to liquid chromatographic columns, it is emphasized that many of the problems described above also relate to gas chromatography, i.e. chromatography wherein the sample and mobile phase are in gaseous, rather than liquid, form.
Indeed, in many respects, the prohlems relate to all packed-bed apparatus comprising a porous mass of particles intended to be intimately and uniformly contacted by a fluid. Such apparatus includes catalytic beds for the treating of gas and liquid, packed beds used in ion exchange processes, in electrophoresis applications, and the like. It is intended that the invention described below be viewed as an improvement in packed-column preparation for all such processes; albeit, the invention will be seen to have particular advantage in the field of liquid chromatography.
In discussing packed-column processes, it is helpful to recognize four kinds of space, all of which can be referred to as "void volume". These include (1) void volume inside a porous particle; (2) theoretical void volume between particles, i~e,the type of unavoidable volume which would result from a perfectly packed bed of spheres of the same size; (3) void volume which is attributable to imperfect packing of particles, usually present to some extent in any actual system utili~ing a particulate packing system; and (4) void volume which represents relatively large voids resulting from the consolidation of those voids described in (3).
Voids (4) substantially reduce resolution of a sample being subjected to chromatographic analysis.
7g5 The invention to be disclosed below is believed to be most useful in avoiding the occurrence of such void volume as described in (4). The present invention also tends to reduce void volume as described in (3); moreover, it makes such void volume more nearly uniform, and closer to a theoretical idea. Void volume, as generally used herein relates to a composite of void volumes (3)and (4).
Some workers have suggested compression of the packing of a chromatographic column by force directed longi-tudinally, i.e. parallel to the direction of liquid flow.However, such a proeedure is relatively ineffective probably because the packing tends to bridge the column and interfere with propogation of the compression force downwardly throughout the length of the column. An example of such work is described in the Journal of Chromatoaraphie Seience of Oetober, 1974, in an artiele entitled "Deseription and Performance of an 8 em. i.d. Column For Preparative Scale High Pressure Liquid-Solid Chromatography" by Godbille and Devaux.
The above discussion of the sac~ground of the Invention is made, neeessarily, in view of the Applieants' invention to be deseribed below. It should be understood that the eollection, interpretation and discussion of this baekground is not intended to disclose the background from the point of view of one being ordinarily skilled in the art and having no preliminary knowledge of Applicant's invention.
Summary of the Invention Therefore, it is an object of the present invention to provide a novel column structure for use in chromatographic applications wherein the column will exhibit improved uniformity of separating eharacteristics over its product life.
78$
Another object of the invention is to provide a package for shipment of chromatographic packing which package is readily converted into a dependable chromatographic column free of any undesirable voids.
Another object of the invention is to provide improved processes for making and operating chromatographic columns.
Still another and broader object of the invention is to provide improved packed columns for use in fluid- --contacting processes whatever the chemical nature of the packing or the physical form of the fluid passed therethrough.
Another object of the invention is to provide a novel means for preparing chromatographic columns which provides an improved column-to-column uniformity of separating characteristics.
Still another object of the invention is to provide a column which may tolerate transportation stresses without substantial reduction in the column's eventual performance.
A further object of the invention is to provide a process for making a chromatographic column with such a high degree of reliability that pre-testing of performance characteristics become unnecessary.
A further object of the invention is to provide an inexpensive r high-quality chromatographic column which can be a disposable item in many, perhaps most, commercial processing situations.
Another object of the invention is to provide apparatus and process means for reestablishing excellent sample resolution in a chromatographic column after the packing therein has been disturbed.
78~i Another object of the invention is to prepare liquid chromatography apparatus which is easily packed and which can be easily repaired, e.g., by adding new packing or changing the packing.
Still another object of the invention is to provide a column which can be readily "healed" if, somehow, excessive voids appear in the packing as might occur, for example, if packing beads break.
Another object of the invention is the achievement of a column having superior resolution characteristics compared to previously-known columns of like diameter and packing, -e.g. a smaller time-concentration profiles of sample components as they emerge from the column.
Other objects of the invention will be obvious to those skilled in the art on reading the objects of this invention.
The above objects have been achieved as a consequence of the discovery that radial compression of the packing within a chromatographic column during the use thereof greatly improves the quality and uniformity of the performance character-istics of the chromatographic column so compressed.
In the most simple case, the column can be filled with packing and compressed just before its use by external pressure acting on the cylindrical wall of the column, e.g.
a wall formed of material such as a thin polyethylene, a polytetrafluoroethylene polymer, or like sheet material.
The wall is surrounded by a pressure chamber and pressed inwardly about the entire cylindrical bed, thereby compressing the particles slightly and achieving better uniformity through-out the bed. The pressure applied to the bed, preferably should not exceed the lateral, radial, yield point of anyportion of the bed, should not cause substantial breaking of particles, and should not exceed the pressure at which the mechanical stability of the wall is maintained. If this happens, there will tend to be a distortion in the uniformity of the cross-sectional size or shape of the bed which is, generally, undesirable and tends to make the desired consistency of the properties of the bed more difficult to achieve. Usually, excellent results can be obtained well below this yield point and the determination thereof is only of academic interest. The yield point, in some case, might result from breaking or gross displacement of particles.
As will be indicated below, it is often preferred to pre-pressurize some of the column packages before they are shipped. This guarantees a predictable uniformity of the commercial product. It is emphasized that such pre-pressurizing, or the filling of a pre-expanded column structure, is not necessary to the practice of this invention.
There are a number of alternate ways the radial pressure can be applied: It can be applied by use of mechanical as well as fluid means. It can be applied from the interior of the column as well as the exterior of the column. Pressure from the exterior of the column is believed to be more desirable because it does not increase the complexity of construction of the column. However, since one of the substantial advantages of the invention is the improved performance and consistency of relatively large diameter columns used in preparative (as opposed to merely analytical) work, internal radial compression is sometimes desirable to maximize the distribution .. .. , ~
of vectors contributing to the radial compression for particu- :
late packing materials. This is believed to be especially so in columns of up to a foot, or even 10 feet, in diameter.
~If gas is used as a pressurizing medium, consideration should be given to the permeability of the wall material to the gas being used. Coatings of less gas permeable materials may be indicated in some circumstances.) In this connection, it can be noted that in most particulate systems any force imposed upon one site will, at some distance from the site, be attenuated to a relatively small and ineffectual force. This invention, in its most advantageous mode, will have every part of the column packing within the a-foresaid distance (which may be called a "radius of fluidity") from the portion of the column.wherein a force-manifesting strain is imposed.
As indicated above, the pressure applied to a given column should be below the radial yield point of the particular packing mass utilized. The yield point itself.will depend on such factors as (1) the nature of the packing and (2) the way the column is packed.
Thus, a column which has been packed:using a special procedure such as.slurry or other techniques adapted to achieve a more densely-packed column, will often be able to withstand a.somewhat higher pressure than will a column containing the.same column packing w~ich has been compacted to a lesser degree. Ne~ertheless, in many circumstances, the above considerations become moot, because there simply is no reason to use the more expensive column-filling techniques when the column is to be operated in such a way as to achieve the processing benefits achieved by practice of the process of the invention. A light .
tapping technique is entirely suitable for filling columns to be operated according to the invention.
In general, satisfactory exterior pressures also depend upon the ease of deformability of the wall, i.e. the force required to push the wall inwardly towards the particles. In a column of 2.25-inch inside diameter and about one foot in length, the following pressure differ~ntials were found to be useful.
Wall Material External Jacket Pressure less Internal Column Pressure low density polyethylene about 75 psig 0.006-inch wall polytetrafluoroethylene about 200 psig 0.030-inch wall These parameters were measured in tests wherein the interior operating pressures of the chromatographic columns ranged from 50 to about 500 psig in this series of experiments.
The invention is a much improved way to avoid packing bed voids. The invention is also believed to be an excellent way of reducing~ indeed virtually overcoming, wall channeling effects whereby liquid preferentially flows through space at the interface of the column wall and the packing. This is particularly true when a distensible wall (such as organic resin walls formed of polyethylene of halogenated hydrocarbon polymers such as that sold under the trade designation "Teflon" by E.I duPont ~eNemours) is utilized. Notwithstanding the special advantage achievable ~ -by reducing wall channeling, the "radial-compression"
process described herein allows a column to be repressurized time and again to what is substantially the same condition throughout its volume. The result of this is that a X
7~
column produced and operated according to the invention is more dependable for a series of comparative experiments than any comparable liquid chromatographic columns known to the art. How~ver, this effect is of major importance even if the column is used only once, because its packing characteristics will be much more dependable when the column is subject to radial compression. Indeed~ in columns of larger diameter, e.g. those of over about one inch in diameter, the primary improvements are largely due to the uniform packing achieved by the radial compression.
For a given particle size, the undesirable effect of wall channeling in such large columns has beenl usually, small in comparison to other imperfections in the packing arrangement.
Distensible polymers include elastomers and rubbers of various types. However, it is important to remember that a chemically inert surface is required for most chemical operations land especially for liquid chromatographic analysis). Consequent polyolefins and halo~enated hydrocarbon polymers like~Teflon are preferred. Another highly desirable characteristic of the distensible polymer is a "memory" characteristic well-known to the art and possessed by many plastics like polyethylene and Teflon. This characteristic might be more aptly expressed~ in the present situation, as an ability to "forget" the shape assumed during a first pressurization against the packing material and an ability to assume a new shape if later pressed and molded against the packing material after it has been disturbed by movement and shifted relative to the polymeric wall surface.
~ 12 -Another aspect of the present invention is the fact that high performance liquid chromatography columns, even those o~ the type used in high-pressure liquid chroma-tography (HPLCl can now be manufactured in a large variety of configurations. The best-known prior art techniques of column-filling utilized special-frequency vibrations or settling of particles from a slurry pumped through the tube. Each of these techniques was basically a s~ttling technique utilizing gravitational force and best-suited for use with a elongate 'cylinder. The present invention can be used in any conEiguration including tubes, coils, U-shapes or the like~ However, it should be realized that, in many such configurations~ the present invention ~' will merely minimize the effect of inherent disadvantages caused by such disadvantages as the lack of equidistant fluid paths through the configuration. These shapes can be oriented vertically or horizontally, the only limitation being that they be so shaped that each segment thereof may be subjected to force vectors generally directed
typical utility of the process is to identify various chemical components in an unknown sample. This identification is made by (1) using an immobile phase which differentially retards the progress of different components of the sample through the column so that the components are separated and leave the column at different times and (2) continuously analyzing the effluent of the column over a period of time.
The separation ls achieved when one component of the sample has more affinity for the stationary phase than does another component. Also, the separation may be achieved by an exclusion process based on the difference in sizes between molecules, e.g., by gel-permeation chromatography processes. The invention to be described below is related to achieving better and more dependable identity of the sample components by improving the efficiency of the process in such a way as to provide better resolution of the sample.
In order to achieve separation of sample components which are very close to each other in chemical and physical .' 7~5 properties, highly sophisticated procedures have been developed in the many processing techniques associated with liquid chromatography. Special pumps and valves have been developed for presenting sample to the inlet of the chromatographic columns with as much integrity as is possible to avoid building into the process an initial and inherent dispersal of the sample which dispersal would tend to reduce the resolution capabilities of the chromatographic packing within the column.
Moreover, much work has been done to provide flow-distributing devices at the inlet of the column to assure the even place-ment of the sample across the column's cross-sectional area.
Also, a great deal of technical effort has provided improved chromatographic packings and highly-sophisticated analytical apparatus for measuring various properties of the liquid effluent leaving the column.
Despite such work as has been described above, it has remained a problem to achieve a unifo~m packing of the chromatographic material into a column. Many techniques have been suggested including vibration (See U.S. Patent 20 3,300,849): All of these techniques require careful control if segregation of particles by size is to be avoided and -uniformly packed columns are to be obtained. Even after the column is filled, problems exist in maintaining the filling in proper condition during transportation and operation of the packed columns. (See patent 3,349,920 to Waters) In general, the most commonly used practice of filling a high-performance column has been a costly method including slurrying the packing and passing the slurry into the column; thereby, in effect, using the column itself as a form for placing a "filter cake" of chromatographic X' packing therein. Even this costly, time-consuming method of column manufacture is not without problems caused by shifting of the packing during shipment when it can be subjected to various vibration and other transient, non-predictable physical abuse. This tends to cause voids in the column and such voids can wholly destroy a column's operating character-istics for many separations. Such defects in stainless steel columns are not usually detectable until a standard sample is measured as a control. Indeed, suppliers of quality chromatographic columns, until this day, have pre-tested individually each column before shipment to the customer to assure that the packing is properly placed in the column.
Of course, this "certifying procedure" provides no protection against the hazards encountered during shipment or during use by the customer. -~
A number of solutions have been suggested for holding the packing "in-place". Some of these, like the aforementioned vibration technique and slurrying technique, emphasize a maximum effort to put a conventional packing into the column in such a way as to have it assume a stable position. Other techniques such as those described in U.S.
patent 3,808,125 to Good use rather complex or expensive procedures for fastenin~ the packing to the column wall.
None of these attempts by the prior art have been dependably successful in achieving any of an excellent perform-ance, a column-to-column consistency in separating character- -istics, or a desired degree of stability of performance over a period of time for a single column, at a cost which can make the apparatus available to the broadest spectrum of chromatographers.
s Although the foregoing description of problems relating to chromatographic columns has been largely devoted to liquid chromatographic columns, it is emphasized that many of the problems described above also relate to gas chromatography, i.e. chromatography wherein the sample and mobile phase are in gaseous, rather than liquid, form.
Indeed, in many respects, the prohlems relate to all packed-bed apparatus comprising a porous mass of particles intended to be intimately and uniformly contacted by a fluid. Such apparatus includes catalytic beds for the treating of gas and liquid, packed beds used in ion exchange processes, in electrophoresis applications, and the like. It is intended that the invention described below be viewed as an improvement in packed-column preparation for all such processes; albeit, the invention will be seen to have particular advantage in the field of liquid chromatography.
In discussing packed-column processes, it is helpful to recognize four kinds of space, all of which can be referred to as "void volume". These include (1) void volume inside a porous particle; (2) theoretical void volume between particles, i~e,the type of unavoidable volume which would result from a perfectly packed bed of spheres of the same size; (3) void volume which is attributable to imperfect packing of particles, usually present to some extent in any actual system utili~ing a particulate packing system; and (4) void volume which represents relatively large voids resulting from the consolidation of those voids described in (3).
Voids (4) substantially reduce resolution of a sample being subjected to chromatographic analysis.
7g5 The invention to be disclosed below is believed to be most useful in avoiding the occurrence of such void volume as described in (4). The present invention also tends to reduce void volume as described in (3); moreover, it makes such void volume more nearly uniform, and closer to a theoretical idea. Void volume, as generally used herein relates to a composite of void volumes (3)and (4).
Some workers have suggested compression of the packing of a chromatographic column by force directed longi-tudinally, i.e. parallel to the direction of liquid flow.However, such a proeedure is relatively ineffective probably because the packing tends to bridge the column and interfere with propogation of the compression force downwardly throughout the length of the column. An example of such work is described in the Journal of Chromatoaraphie Seience of Oetober, 1974, in an artiele entitled "Deseription and Performance of an 8 em. i.d. Column For Preparative Scale High Pressure Liquid-Solid Chromatography" by Godbille and Devaux.
The above discussion of the sac~ground of the Invention is made, neeessarily, in view of the Applieants' invention to be deseribed below. It should be understood that the eollection, interpretation and discussion of this baekground is not intended to disclose the background from the point of view of one being ordinarily skilled in the art and having no preliminary knowledge of Applicant's invention.
Summary of the Invention Therefore, it is an object of the present invention to provide a novel column structure for use in chromatographic applications wherein the column will exhibit improved uniformity of separating eharacteristics over its product life.
78$
Another object of the invention is to provide a package for shipment of chromatographic packing which package is readily converted into a dependable chromatographic column free of any undesirable voids.
Another object of the invention is to provide improved processes for making and operating chromatographic columns.
Still another and broader object of the invention is to provide improved packed columns for use in fluid- --contacting processes whatever the chemical nature of the packing or the physical form of the fluid passed therethrough.
Another object of the invention is to provide a novel means for preparing chromatographic columns which provides an improved column-to-column uniformity of separating characteristics.
Still another object of the invention is to provide a column which may tolerate transportation stresses without substantial reduction in the column's eventual performance.
A further object of the invention is to provide a process for making a chromatographic column with such a high degree of reliability that pre-testing of performance characteristics become unnecessary.
A further object of the invention is to provide an inexpensive r high-quality chromatographic column which can be a disposable item in many, perhaps most, commercial processing situations.
Another object of the invention is to provide apparatus and process means for reestablishing excellent sample resolution in a chromatographic column after the packing therein has been disturbed.
78~i Another object of the invention is to prepare liquid chromatography apparatus which is easily packed and which can be easily repaired, e.g., by adding new packing or changing the packing.
Still another object of the invention is to provide a column which can be readily "healed" if, somehow, excessive voids appear in the packing as might occur, for example, if packing beads break.
Another object of the invention is the achievement of a column having superior resolution characteristics compared to previously-known columns of like diameter and packing, -e.g. a smaller time-concentration profiles of sample components as they emerge from the column.
Other objects of the invention will be obvious to those skilled in the art on reading the objects of this invention.
The above objects have been achieved as a consequence of the discovery that radial compression of the packing within a chromatographic column during the use thereof greatly improves the quality and uniformity of the performance character-istics of the chromatographic column so compressed.
In the most simple case, the column can be filled with packing and compressed just before its use by external pressure acting on the cylindrical wall of the column, e.g.
a wall formed of material such as a thin polyethylene, a polytetrafluoroethylene polymer, or like sheet material.
The wall is surrounded by a pressure chamber and pressed inwardly about the entire cylindrical bed, thereby compressing the particles slightly and achieving better uniformity through-out the bed. The pressure applied to the bed, preferably should not exceed the lateral, radial, yield point of anyportion of the bed, should not cause substantial breaking of particles, and should not exceed the pressure at which the mechanical stability of the wall is maintained. If this happens, there will tend to be a distortion in the uniformity of the cross-sectional size or shape of the bed which is, generally, undesirable and tends to make the desired consistency of the properties of the bed more difficult to achieve. Usually, excellent results can be obtained well below this yield point and the determination thereof is only of academic interest. The yield point, in some case, might result from breaking or gross displacement of particles.
As will be indicated below, it is often preferred to pre-pressurize some of the column packages before they are shipped. This guarantees a predictable uniformity of the commercial product. It is emphasized that such pre-pressurizing, or the filling of a pre-expanded column structure, is not necessary to the practice of this invention.
There are a number of alternate ways the radial pressure can be applied: It can be applied by use of mechanical as well as fluid means. It can be applied from the interior of the column as well as the exterior of the column. Pressure from the exterior of the column is believed to be more desirable because it does not increase the complexity of construction of the column. However, since one of the substantial advantages of the invention is the improved performance and consistency of relatively large diameter columns used in preparative (as opposed to merely analytical) work, internal radial compression is sometimes desirable to maximize the distribution .. .. , ~
of vectors contributing to the radial compression for particu- :
late packing materials. This is believed to be especially so in columns of up to a foot, or even 10 feet, in diameter.
~If gas is used as a pressurizing medium, consideration should be given to the permeability of the wall material to the gas being used. Coatings of less gas permeable materials may be indicated in some circumstances.) In this connection, it can be noted that in most particulate systems any force imposed upon one site will, at some distance from the site, be attenuated to a relatively small and ineffectual force. This invention, in its most advantageous mode, will have every part of the column packing within the a-foresaid distance (which may be called a "radius of fluidity") from the portion of the column.wherein a force-manifesting strain is imposed.
As indicated above, the pressure applied to a given column should be below the radial yield point of the particular packing mass utilized. The yield point itself.will depend on such factors as (1) the nature of the packing and (2) the way the column is packed.
Thus, a column which has been packed:using a special procedure such as.slurry or other techniques adapted to achieve a more densely-packed column, will often be able to withstand a.somewhat higher pressure than will a column containing the.same column packing w~ich has been compacted to a lesser degree. Ne~ertheless, in many circumstances, the above considerations become moot, because there simply is no reason to use the more expensive column-filling techniques when the column is to be operated in such a way as to achieve the processing benefits achieved by practice of the process of the invention. A light .
tapping technique is entirely suitable for filling columns to be operated according to the invention.
In general, satisfactory exterior pressures also depend upon the ease of deformability of the wall, i.e. the force required to push the wall inwardly towards the particles. In a column of 2.25-inch inside diameter and about one foot in length, the following pressure differ~ntials were found to be useful.
Wall Material External Jacket Pressure less Internal Column Pressure low density polyethylene about 75 psig 0.006-inch wall polytetrafluoroethylene about 200 psig 0.030-inch wall These parameters were measured in tests wherein the interior operating pressures of the chromatographic columns ranged from 50 to about 500 psig in this series of experiments.
The invention is a much improved way to avoid packing bed voids. The invention is also believed to be an excellent way of reducing~ indeed virtually overcoming, wall channeling effects whereby liquid preferentially flows through space at the interface of the column wall and the packing. This is particularly true when a distensible wall (such as organic resin walls formed of polyethylene of halogenated hydrocarbon polymers such as that sold under the trade designation "Teflon" by E.I duPont ~eNemours) is utilized. Notwithstanding the special advantage achievable ~ -by reducing wall channeling, the "radial-compression"
process described herein allows a column to be repressurized time and again to what is substantially the same condition throughout its volume. The result of this is that a X
7~
column produced and operated according to the invention is more dependable for a series of comparative experiments than any comparable liquid chromatographic columns known to the art. How~ver, this effect is of major importance even if the column is used only once, because its packing characteristics will be much more dependable when the column is subject to radial compression. Indeed~ in columns of larger diameter, e.g. those of over about one inch in diameter, the primary improvements are largely due to the uniform packing achieved by the radial compression.
For a given particle size, the undesirable effect of wall channeling in such large columns has beenl usually, small in comparison to other imperfections in the packing arrangement.
Distensible polymers include elastomers and rubbers of various types. However, it is important to remember that a chemically inert surface is required for most chemical operations land especially for liquid chromatographic analysis). Consequent polyolefins and halo~enated hydrocarbon polymers like~Teflon are preferred. Another highly desirable characteristic of the distensible polymer is a "memory" characteristic well-known to the art and possessed by many plastics like polyethylene and Teflon. This characteristic might be more aptly expressed~ in the present situation, as an ability to "forget" the shape assumed during a first pressurization against the packing material and an ability to assume a new shape if later pressed and molded against the packing material after it has been disturbed by movement and shifted relative to the polymeric wall surface.
~ 12 -Another aspect of the present invention is the fact that high performance liquid chromatography columns, even those o~ the type used in high-pressure liquid chroma-tography (HPLCl can now be manufactured in a large variety of configurations. The best-known prior art techniques of column-filling utilized special-frequency vibrations or settling of particles from a slurry pumped through the tube. Each of these techniques was basically a s~ttling technique utilizing gravitational force and best-suited for use with a elongate 'cylinder. The present invention can be used in any conEiguration including tubes, coils, U-shapes or the like~ However, it should be realized that, in many such configurations~ the present invention ~' will merely minimize the effect of inherent disadvantages caused by such disadvantages as the lack of equidistant fluid paths through the configuration. These shapes can be oriented vertically or horizontally, the only limitation being that they be so shaped that each segment thereof may be subjected to force vectors generally directed
2~ from the outer walls thereof towards the center of the configuration - a condition described as "radial compression"
in this application Another means for obtaining the desirable radial compression is to form a rigid column, say a steel tube, which has a coating of a deformable material, say a coating of a plastic such as poly (tetrafluoroethylene), polyethylene, or the like on inside thereof~ The coating is preferably chemically inert and among current commercial materials, poly (tetrafluoroethylene) is a preferred coating. The coated tube is expanded, e.g. by heat or pressure or both, filled with a packing material and then allowed to contract. This contracting resuIts in a radial compression of the packing particles, with the steel wall acting as a diaphragm. The particles are pushed into the plastic coating to the extent that wall-channeling is virtually eliminated. Residual compression is sufficient to achieve the uniformity of packing compaction that has been described for the externally-applied pressure aspect of this invention.
There is some advantage to use of a prestressed column where in the chamber wall structure is formed of a relatively non-flexible material like steel~ Such a column avoids any marked gradient in-differential pressure between the entrance of a column and the exterior of -a column. Thus, at higher column operating pressures, there can be no tendency for a packing to be moved from the bottom of the column (where a relatively high pressure differential would be experienced using a flimsy, otherwise non-structured, retaining package) towards the top of the column (where the high internal pressure in the column itself would be much closer to the pressure exerted on the exterior of a relatively flimsy, otherwise non-structured, retaining package).
Also, the prestressed columns have advantage in many low pressure operations wherein the particles are soft, or spongy, or have internal porosity which must be prestress and, consequently, where very close control of the strain on the particles must be exerted all along the length of the column.
AS may be deduced from the above, in largerdiameter columns, where wall channeling is not a substantial factor, the above-described pre-compressed metal columns can be used advantageously without a distensible material adapted for conforming to the surface of the packing particles in response to the opposite force exerted by the particles on the surface. This distension reduces the void volume at the interface of said mass of particles with the metal wall of column. "Distensible" in the sense used here means ability to conform to the irregularities of diverse particles in the surface of the mass of packing and to subs~ntially reduce the channeling volume between the packing and the wall.
It is also possible to expand polymeric columns, fill them with packing, and allow them to contract to exert the proper radial pressure on the packing without the need of maintaining an external pressure~ However, it is believed that this procedure is best avoided because of the unpredictable nature of conditions to be encountered in transportation of such columns. Nevertheless, it should be noted that such columns can be prepared. Indeed, a small amount of expansion is also advantageously utilized before packing thin-wall plastic columns, but this is done to eliminate ripples and bulges in the compressed wall, a cosmetic advantage to facilitate the filling operations and assure a proper initial packing procedure rather than permanently prestress a diaphragm wall.
It has been found that those advantages of the instant invention relating to a) reduction or elimination of wall channeling and b) a more uniform packing also : -s allow optimization of the effects of flow-distributing techniques at the head of a column. That is, the flow-distributing techniques-known to the prior art tend to work better when utilized in columns constructed and operated according to the instant invention. Moreover, the instant invention makes the further optimization of flow-distribution apparatus practical and desirable because the packed column is, in many cases, no longer the limiting factor in achieving good uniform flow distri-bution.
"Bridging" is a phenomena wherein packing arrangesitself in such a mechanical relationship with the walls of a column that an arch-like resistance is formed to compression of the packing in directions generally parallel to the walIs.
One of the advantages of the instant invention is to avoid bridging interference resistance to effective compression of the columns. However, it should be realized, that by radial compression, it is also possible to effect an improved bridging phenomena ~7herein vertical incremen's of packing are isolated by bridges which are relatively close to another. As the bridges become very close to one another, an improved chromatographic column is produced which can be successfully operated at higher pressures than a column containing the same packing which has been operated with prior art techniques. This is so because each bridge protects those particles below it from the pressure exerted above that bridge.
The most advantageous use of this increased 0 bridge frequency is in using relatively soft compressible packing materials such as a relatively large-pore, lightly-crosslinked polymeric packing material sold under the trade designation Sephadex~ Advantage is also achieved with somewhat smaller-pore, more crosslinked materials sold under the same trade designation. Such materials are very well known in the art. Somewhat less advantage is achieved with less compressible materials, and the increased bridging is not believed to make a major contribution to the improved performance of alumina and silica-type packing materials, the improved performance of such packing materials in the practice of the instant invention is believed to be primarily due to factors discussed elsewhere in this disclosure.
When gas is used to pressuri2e the column, it may be desirable to use a wall-material which has a gas-impermeable barrier layer. Various polymeric coating materials are known to be particularly resistant to passage of particular gases and may be used. Also, thin metallic foils may be incorporated between or used in conjunction with or in place of polymeric films to form suitable column wall structures.
Illustrative Examples of the Invention In this application and accompanying drawings there is shown and described a preferred embodiment of the invention and suggested various alternatives and :
modifications thereof, but it is to be understood that these are not intended to be exhaustive and that other --changes and modifications can be made within the scope -of the invention. These suggestions herein are selected and included for purposes of illustration in order that others skilled in the art will more fuIly understand the invention and the principles thereof and will be able to modify it and embody it in a variety of forms, each as may be best suited in the condition of a particular case.
Figures one through nine are sections of a column illustrating steps used to form an externally pressurized column, and the novel compression columns formed by said steps.
Figures 10-13 illustrate schematically those steps used to form a column having an exterior compression cylinder lined with a deformable polymeric coating according to the invention and the novel compression column formed by said steps.
Figures 14a and 14b illustrate schematically various configurations of chromatographic tubes which can be advantageously filled according to the invention:
These are set out to illustrate one novel aspect of column construction made possible by practice of the invention, i.e. the construction of packed beds which are suitably packed although shaped with conical (Figure 14a) sinusoidal (Figure 14B), or other elongate passages which are not reliably packed using the packing techniques of the prior art.
Figure 15 is a schematic showing the cross section of a cylindrical column about which are mounted mechanically actuated compressing means.
Figure 1 ill-ustrates a polytetrafluoroethylene tubing 30 of about 0.030 inch wall thickness, 12 inches long and about 2 inches in tubing diameter. Figure 2 : , . :
~3~8~i illustrates the placement of the tube in a packing chamber 32. Figure 3 shows a porous glass-frit plug 38 inserted into the bottom end of the tube to hold it snugly in the packing chamber. A plug 34 is inserted in the top.
Gas is admitted into the tube 30 through conduit 36 and plug 34 to obtain an expansion thereof as seen in Figure 4. Air pressure is used to achieve an expansion of about 15% in volume.
Plug 34 is removed. (Fig. 5) Then the tube is filled with a chromatographic packing material, 60-200 mesh silica-based packing. Only a slight tapping or shaking action need be used in filling the column.
A glass frit 38 (Fig. 6) is inserted at the top of the column and end caps 39 are bolted on to form a pressure chamber.
Figure 7 illustrates the radial compression as gas at 250 psig is admitted into chamber 32 through valve 40 to achieve an initial radial compression of the tube. End caps 42 ~Fig. 8l are snapped over the column after it is removed from the packing chamber 32, for protection of the column during shipment.
The column is then ready for shipment. When received, end caps are removed, and it is placed into a pressure vessel ~Fig. 9) such as 50. Gasketed end plates 51 are bolted down with bolts 52, and in general such good practice as is known in the art is followed in manufacture and use of such pressure vessels. In use, the tube is externally pressurized to about 200 psig above the operating pressure of a li~uid chromatographic process as measured at the head of the column.
-- 19 -- :
7~
The same procedure is repeated using a medium density polyethylene film. The film was heated to about 110C to facilitate its pre-fill expansion to 15~. Such heating resulted in a snug, superior fit of the film over the packing when after compression the film was cooled and allowed to shrink to form a taut package~
Indeed, the fit would allow the column to be utilized advantageous at low pressures, say below about 100 psi~
However, the column tends to "loosen up" a bit on storage and repressurization is required for the illustrated construction.
Figure 10 illustrates a steel tube 60 (316 stainless steel) of a wall thickness of 0.080 inch and an inside diameter dl of about 0.25 inch. The tube is placed in a heat exchanger schematically shown at 61 and heated from 25C to 85C. Simultaneously a slurry of 10-micron silica-based chromatography packing is run through the column in order to deposit the packing according to the well-known slurry techniques. The combination of the pressurized slurry and the heated tube expands the tube during the filling operation substantially to a diameter d2 as seen in Figure 11.
When the tube is allowed to return to room temperature as seen in Figure 12, it radially compresses the packing according to the invention. If a wall channel effect is to be avoided or minimized, it is most desirable to utilize a metal tube 62 (Fig. 13~ with its wall 64 coated with about 0~001 inch of a polytetrafluoroethylene polymer 66 which is distensible under the radial compression to conform substantially to the shape of the packing material 69 at interface 68, thereby avoiding highly :~0~78S
undesirable wall channeling.
The columns described in Figure 10-13 are fitted with and include end fittings, as are other columns sold in the chromatographic art, and are shipped pre-compressed for direct use. Their radial compression is permanent:
they do not usually require any further compression steps as long as the same packing remains in the column~
A number of simple mechanical means can be used to achieve the required radial compression. These are advantageously constructed so that they reduce the cross-section of the column all the way along its length, i.e. inlet end fitting to outlet fitting~ The shrinking of a heat expande~ tube is a species of such mechanical means wherein the tube itself is the radial compressing means. In other embodiments of the invention, flexible wall tubes formed of foil, plastic film, or the like are distorted, as from a circular to non-circular cross section, by an external means such as a cam or like device which is forced against the wall to change its shape in such a way as to reduce its cross-sectional area.
A decrease in cross-sectional areaJ typically as little as a 2 to 5 change, is effective in well-packed columns, decreases of over about 10% are seldom required, Figure 15 is illustrative of a column equipped with such mechanical pressurizing means. Column 80 comprises a tube formed of 0.030-mil thick polytetrafluoroethylene.
It is mounted with 4 cams 82 mounted thereabout in a normal position indicated in solid lines where they do not press into the wall 84. These cams extend along the entire length 7~35 of flexible column wall ~l. When it is desired to anply radial compression, the cams are turned to the position defined by the dotted lines and they so compress packing 86 that the desired amount of radial compression is achieved.
As in other aspects of the invention, a distensible polymer surface is advantageous at the interface between column wall and packing.
It is no part of this invention to discuss in detail those well-known aspects of the mechanical arts which can be utilized in devising various means to assure proper compression. Those skilled in the art will be able to devise many such quick-actuating devices capable of performing according to the teaching of this invention. In general, however, it is desirable to have at least two or three different ~ -pressure sites on a given column; although in shorter columns, one pressure site can be very effective.
Figure 15 is also illustrative of the broad scope - ~-radial compression is intended to have. Obviously the vectors emanating from the pressure points caused by the cams (des-cribed hereinafter) are not strictly radial nonetheless, they have a substantial, effective, net effect which is radial and act well within the term "radial compression"
as it is used in this specification.
There are numerous other means to provide for a source of strain-inducing pressure on the packed bed.
For example, the bed could be surrounded by a jacket into which a low-melting alloy such as Woods Metal could be poured, pressurized, and allowed to cool and solidify under pressure.
Metals which expand on cooling are preferred. Whenever, repressurization is required to heal, or repack, or repair the packing, the alloy could be melted and repressurized and once again frozen.
Another approach would be to wind a helical wire or tubing or series of circuIar rings about the column and use thermal or pneumatic or mechanical means to change the dimensions of the tubing or rings and produce a strain, that is a reduction of cross-sectional area on the column.
As has been indicated above, an improved flow distribution is achieved whenever a good flow distribution means is employed at the column inlet, and this distribution is maintained with remarkable fidelity throughout the length of a novel radially compressed column of the type disclosed.
It has been found that it is usually most desirable to apply the strain to a packed column before the column is wetted, i.e., before the liquid chromatographic procedure is started. When the prepacked columns such as those formed of polymeric walls are to be used, they will often have "relaxed" somewhat over a period of time after the initial packing. Thus, if they are advantageously repressurized before being wetted, the resulting force is maintained on the column during use.
The term "diaphragm" as used herein means a column wall section that can be moved to impart strain to the packing within the column. Many complex structures can be used to achieve this result. As will be suggested by example below, all of the column wall need not be moved, it is often sufficient to impart strain along a single linear situs along the column wall. Also, it is possible to exert such strain by pushing on a substantial number of sites distributed over the column surface. Walls using all such techniques are "diaphragms" according to this ~eneral use of the term in this disclosure. Such walls may be internal, e.g. in ;~
the center of the column and adapted for movement towards the exterior wall of the column. Nevertheless, it is usually desirable to use one of the relatively simple structures disclosed herein.
There are other ways to place the packing under a suitable,repetitive compressing force. One, is to make ~ -a dynamically balanced column spun at high speed about its axis pushing the packing particles outwardly toward the outer wall of the column. It might well be necessary to have an axially-positioned follower device ~mechanical or hydraulic) which would expand to the extent necessary to fill any space that outwardly-moving particles left. It is the applicants' position that such a device is a mechanical equivalent to the present invention because it would use radial compression and a reduction in effective cross-sectional area of the packing. The primary forces would be outwardly directed in this situation, but the centrifugal device would only be a means for achieving the radial compression. In such a situation, the one operation achievement of compression and taking-up of void volume created by the compression is not achieved, and it is necessary to use the axial follower to take up the void volume. The follower would be means made necessary to avoid a central void from forming, by movement of packing towards the outer wall of the column.
Moreover, a doughnut-shaped column, i.e. one with a hollow axial bore, could be constructed. Not only could pressure be exerted from both internal and external cylindrical walls, but the walls could be used to improve heat transfer properties of the apparatus.
s In general, the term "radial compression" is meant to describe a compression wherein the compression f~rces are predominantly aligned in a direction which is normal to flow of liquid through the column, i.e. in the classical situation of a cylindrical column, the forces would be directed toward the center of the cylinder.
It is to be understood that the following claims are intended to cover all of the generic and specific features of the invention herein described and all statements of the scope of the invention which might be said to fall there-between.
in this application Another means for obtaining the desirable radial compression is to form a rigid column, say a steel tube, which has a coating of a deformable material, say a coating of a plastic such as poly (tetrafluoroethylene), polyethylene, or the like on inside thereof~ The coating is preferably chemically inert and among current commercial materials, poly (tetrafluoroethylene) is a preferred coating. The coated tube is expanded, e.g. by heat or pressure or both, filled with a packing material and then allowed to contract. This contracting resuIts in a radial compression of the packing particles, with the steel wall acting as a diaphragm. The particles are pushed into the plastic coating to the extent that wall-channeling is virtually eliminated. Residual compression is sufficient to achieve the uniformity of packing compaction that has been described for the externally-applied pressure aspect of this invention.
There is some advantage to use of a prestressed column where in the chamber wall structure is formed of a relatively non-flexible material like steel~ Such a column avoids any marked gradient in-differential pressure between the entrance of a column and the exterior of -a column. Thus, at higher column operating pressures, there can be no tendency for a packing to be moved from the bottom of the column (where a relatively high pressure differential would be experienced using a flimsy, otherwise non-structured, retaining package) towards the top of the column (where the high internal pressure in the column itself would be much closer to the pressure exerted on the exterior of a relatively flimsy, otherwise non-structured, retaining package).
Also, the prestressed columns have advantage in many low pressure operations wherein the particles are soft, or spongy, or have internal porosity which must be prestress and, consequently, where very close control of the strain on the particles must be exerted all along the length of the column.
AS may be deduced from the above, in largerdiameter columns, where wall channeling is not a substantial factor, the above-described pre-compressed metal columns can be used advantageously without a distensible material adapted for conforming to the surface of the packing particles in response to the opposite force exerted by the particles on the surface. This distension reduces the void volume at the interface of said mass of particles with the metal wall of column. "Distensible" in the sense used here means ability to conform to the irregularities of diverse particles in the surface of the mass of packing and to subs~ntially reduce the channeling volume between the packing and the wall.
It is also possible to expand polymeric columns, fill them with packing, and allow them to contract to exert the proper radial pressure on the packing without the need of maintaining an external pressure~ However, it is believed that this procedure is best avoided because of the unpredictable nature of conditions to be encountered in transportation of such columns. Nevertheless, it should be noted that such columns can be prepared. Indeed, a small amount of expansion is also advantageously utilized before packing thin-wall plastic columns, but this is done to eliminate ripples and bulges in the compressed wall, a cosmetic advantage to facilitate the filling operations and assure a proper initial packing procedure rather than permanently prestress a diaphragm wall.
It has been found that those advantages of the instant invention relating to a) reduction or elimination of wall channeling and b) a more uniform packing also : -s allow optimization of the effects of flow-distributing techniques at the head of a column. That is, the flow-distributing techniques-known to the prior art tend to work better when utilized in columns constructed and operated according to the instant invention. Moreover, the instant invention makes the further optimization of flow-distribution apparatus practical and desirable because the packed column is, in many cases, no longer the limiting factor in achieving good uniform flow distri-bution.
"Bridging" is a phenomena wherein packing arrangesitself in such a mechanical relationship with the walls of a column that an arch-like resistance is formed to compression of the packing in directions generally parallel to the walIs.
One of the advantages of the instant invention is to avoid bridging interference resistance to effective compression of the columns. However, it should be realized, that by radial compression, it is also possible to effect an improved bridging phenomena ~7herein vertical incremen's of packing are isolated by bridges which are relatively close to another. As the bridges become very close to one another, an improved chromatographic column is produced which can be successfully operated at higher pressures than a column containing the same packing which has been operated with prior art techniques. This is so because each bridge protects those particles below it from the pressure exerted above that bridge.
The most advantageous use of this increased 0 bridge frequency is in using relatively soft compressible packing materials such as a relatively large-pore, lightly-crosslinked polymeric packing material sold under the trade designation Sephadex~ Advantage is also achieved with somewhat smaller-pore, more crosslinked materials sold under the same trade designation. Such materials are very well known in the art. Somewhat less advantage is achieved with less compressible materials, and the increased bridging is not believed to make a major contribution to the improved performance of alumina and silica-type packing materials, the improved performance of such packing materials in the practice of the instant invention is believed to be primarily due to factors discussed elsewhere in this disclosure.
When gas is used to pressuri2e the column, it may be desirable to use a wall-material which has a gas-impermeable barrier layer. Various polymeric coating materials are known to be particularly resistant to passage of particular gases and may be used. Also, thin metallic foils may be incorporated between or used in conjunction with or in place of polymeric films to form suitable column wall structures.
Illustrative Examples of the Invention In this application and accompanying drawings there is shown and described a preferred embodiment of the invention and suggested various alternatives and :
modifications thereof, but it is to be understood that these are not intended to be exhaustive and that other --changes and modifications can be made within the scope -of the invention. These suggestions herein are selected and included for purposes of illustration in order that others skilled in the art will more fuIly understand the invention and the principles thereof and will be able to modify it and embody it in a variety of forms, each as may be best suited in the condition of a particular case.
Figures one through nine are sections of a column illustrating steps used to form an externally pressurized column, and the novel compression columns formed by said steps.
Figures 10-13 illustrate schematically those steps used to form a column having an exterior compression cylinder lined with a deformable polymeric coating according to the invention and the novel compression column formed by said steps.
Figures 14a and 14b illustrate schematically various configurations of chromatographic tubes which can be advantageously filled according to the invention:
These are set out to illustrate one novel aspect of column construction made possible by practice of the invention, i.e. the construction of packed beds which are suitably packed although shaped with conical (Figure 14a) sinusoidal (Figure 14B), or other elongate passages which are not reliably packed using the packing techniques of the prior art.
Figure 15 is a schematic showing the cross section of a cylindrical column about which are mounted mechanically actuated compressing means.
Figure 1 ill-ustrates a polytetrafluoroethylene tubing 30 of about 0.030 inch wall thickness, 12 inches long and about 2 inches in tubing diameter. Figure 2 : , . :
~3~8~i illustrates the placement of the tube in a packing chamber 32. Figure 3 shows a porous glass-frit plug 38 inserted into the bottom end of the tube to hold it snugly in the packing chamber. A plug 34 is inserted in the top.
Gas is admitted into the tube 30 through conduit 36 and plug 34 to obtain an expansion thereof as seen in Figure 4. Air pressure is used to achieve an expansion of about 15% in volume.
Plug 34 is removed. (Fig. 5) Then the tube is filled with a chromatographic packing material, 60-200 mesh silica-based packing. Only a slight tapping or shaking action need be used in filling the column.
A glass frit 38 (Fig. 6) is inserted at the top of the column and end caps 39 are bolted on to form a pressure chamber.
Figure 7 illustrates the radial compression as gas at 250 psig is admitted into chamber 32 through valve 40 to achieve an initial radial compression of the tube. End caps 42 ~Fig. 8l are snapped over the column after it is removed from the packing chamber 32, for protection of the column during shipment.
The column is then ready for shipment. When received, end caps are removed, and it is placed into a pressure vessel ~Fig. 9) such as 50. Gasketed end plates 51 are bolted down with bolts 52, and in general such good practice as is known in the art is followed in manufacture and use of such pressure vessels. In use, the tube is externally pressurized to about 200 psig above the operating pressure of a li~uid chromatographic process as measured at the head of the column.
-- 19 -- :
7~
The same procedure is repeated using a medium density polyethylene film. The film was heated to about 110C to facilitate its pre-fill expansion to 15~. Such heating resulted in a snug, superior fit of the film over the packing when after compression the film was cooled and allowed to shrink to form a taut package~
Indeed, the fit would allow the column to be utilized advantageous at low pressures, say below about 100 psi~
However, the column tends to "loosen up" a bit on storage and repressurization is required for the illustrated construction.
Figure 10 illustrates a steel tube 60 (316 stainless steel) of a wall thickness of 0.080 inch and an inside diameter dl of about 0.25 inch. The tube is placed in a heat exchanger schematically shown at 61 and heated from 25C to 85C. Simultaneously a slurry of 10-micron silica-based chromatography packing is run through the column in order to deposit the packing according to the well-known slurry techniques. The combination of the pressurized slurry and the heated tube expands the tube during the filling operation substantially to a diameter d2 as seen in Figure 11.
When the tube is allowed to return to room temperature as seen in Figure 12, it radially compresses the packing according to the invention. If a wall channel effect is to be avoided or minimized, it is most desirable to utilize a metal tube 62 (Fig. 13~ with its wall 64 coated with about 0~001 inch of a polytetrafluoroethylene polymer 66 which is distensible under the radial compression to conform substantially to the shape of the packing material 69 at interface 68, thereby avoiding highly :~0~78S
undesirable wall channeling.
The columns described in Figure 10-13 are fitted with and include end fittings, as are other columns sold in the chromatographic art, and are shipped pre-compressed for direct use. Their radial compression is permanent:
they do not usually require any further compression steps as long as the same packing remains in the column~
A number of simple mechanical means can be used to achieve the required radial compression. These are advantageously constructed so that they reduce the cross-section of the column all the way along its length, i.e. inlet end fitting to outlet fitting~ The shrinking of a heat expande~ tube is a species of such mechanical means wherein the tube itself is the radial compressing means. In other embodiments of the invention, flexible wall tubes formed of foil, plastic film, or the like are distorted, as from a circular to non-circular cross section, by an external means such as a cam or like device which is forced against the wall to change its shape in such a way as to reduce its cross-sectional area.
A decrease in cross-sectional areaJ typically as little as a 2 to 5 change, is effective in well-packed columns, decreases of over about 10% are seldom required, Figure 15 is illustrative of a column equipped with such mechanical pressurizing means. Column 80 comprises a tube formed of 0.030-mil thick polytetrafluoroethylene.
It is mounted with 4 cams 82 mounted thereabout in a normal position indicated in solid lines where they do not press into the wall 84. These cams extend along the entire length 7~35 of flexible column wall ~l. When it is desired to anply radial compression, the cams are turned to the position defined by the dotted lines and they so compress packing 86 that the desired amount of radial compression is achieved.
As in other aspects of the invention, a distensible polymer surface is advantageous at the interface between column wall and packing.
It is no part of this invention to discuss in detail those well-known aspects of the mechanical arts which can be utilized in devising various means to assure proper compression. Those skilled in the art will be able to devise many such quick-actuating devices capable of performing according to the teaching of this invention. In general, however, it is desirable to have at least two or three different ~ -pressure sites on a given column; although in shorter columns, one pressure site can be very effective.
Figure 15 is also illustrative of the broad scope - ~-radial compression is intended to have. Obviously the vectors emanating from the pressure points caused by the cams (des-cribed hereinafter) are not strictly radial nonetheless, they have a substantial, effective, net effect which is radial and act well within the term "radial compression"
as it is used in this specification.
There are numerous other means to provide for a source of strain-inducing pressure on the packed bed.
For example, the bed could be surrounded by a jacket into which a low-melting alloy such as Woods Metal could be poured, pressurized, and allowed to cool and solidify under pressure.
Metals which expand on cooling are preferred. Whenever, repressurization is required to heal, or repack, or repair the packing, the alloy could be melted and repressurized and once again frozen.
Another approach would be to wind a helical wire or tubing or series of circuIar rings about the column and use thermal or pneumatic or mechanical means to change the dimensions of the tubing or rings and produce a strain, that is a reduction of cross-sectional area on the column.
As has been indicated above, an improved flow distribution is achieved whenever a good flow distribution means is employed at the column inlet, and this distribution is maintained with remarkable fidelity throughout the length of a novel radially compressed column of the type disclosed.
It has been found that it is usually most desirable to apply the strain to a packed column before the column is wetted, i.e., before the liquid chromatographic procedure is started. When the prepacked columns such as those formed of polymeric walls are to be used, they will often have "relaxed" somewhat over a period of time after the initial packing. Thus, if they are advantageously repressurized before being wetted, the resulting force is maintained on the column during use.
The term "diaphragm" as used herein means a column wall section that can be moved to impart strain to the packing within the column. Many complex structures can be used to achieve this result. As will be suggested by example below, all of the column wall need not be moved, it is often sufficient to impart strain along a single linear situs along the column wall. Also, it is possible to exert such strain by pushing on a substantial number of sites distributed over the column surface. Walls using all such techniques are "diaphragms" according to this ~eneral use of the term in this disclosure. Such walls may be internal, e.g. in ;~
the center of the column and adapted for movement towards the exterior wall of the column. Nevertheless, it is usually desirable to use one of the relatively simple structures disclosed herein.
There are other ways to place the packing under a suitable,repetitive compressing force. One, is to make ~ -a dynamically balanced column spun at high speed about its axis pushing the packing particles outwardly toward the outer wall of the column. It might well be necessary to have an axially-positioned follower device ~mechanical or hydraulic) which would expand to the extent necessary to fill any space that outwardly-moving particles left. It is the applicants' position that such a device is a mechanical equivalent to the present invention because it would use radial compression and a reduction in effective cross-sectional area of the packing. The primary forces would be outwardly directed in this situation, but the centrifugal device would only be a means for achieving the radial compression. In such a situation, the one operation achievement of compression and taking-up of void volume created by the compression is not achieved, and it is necessary to use the axial follower to take up the void volume. The follower would be means made necessary to avoid a central void from forming, by movement of packing towards the outer wall of the column.
Moreover, a doughnut-shaped column, i.e. one with a hollow axial bore, could be constructed. Not only could pressure be exerted from both internal and external cylindrical walls, but the walls could be used to improve heat transfer properties of the apparatus.
s In general, the term "radial compression" is meant to describe a compression wherein the compression f~rces are predominantly aligned in a direction which is normal to flow of liquid through the column, i.e. in the classical situation of a cylindrical column, the forces would be directed toward the center of the cylinder.
It is to be understood that the following claims are intended to cover all of the generic and specific features of the invention herein described and all statements of the scope of the invention which might be said to fall there-between.
Claims (30)
PROPERTY OF PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. Apparatus for chromatography comprising: a chamber containing a porous chromatographic bed of packed particles, inlet and outlet ports for passing fluid through the chamber and through said chromatographic bed therein, and means to compress said chromatographic bed in said chamber radially of the direction of flow so as to reduce void volume associated with the packing of said particles.
2. Apparatus as defined in claim 1 wherein said chamber is an elongate chamber, retaining means at said inlet and outlet holds said porous mass in said chamber, and the wall of said chamber forms a movable dia-phragm which forms said arrangement to radially compress said porous mass.
3. Apparatus as defined in claim 2 wherein said diaphragm has been prestressed so that it sufficiently radially compresses said porous mass to deform and reduce said void volume including that between said diaphragm and said mass without application of pressure to the outside of said dia-phragm.
4. Apparatus as defined in claim 3 wherein said diaphragm comprises an interior wall formed of a distensible organic polymer material said polymer material forming means to press radially against said mass and to conform to the surface of said mass and reduce void volume between said mass and said diaphragm.
5. Apparatus as defined in claim 4 wherein the wall of said chamber is formed of poly(tetrafluoroethylene) or polyethylene.
6. Apparatus as defined in claim 5 wherein said chamber is so con-struted that it forms means to radially compress said mass when a pressure of about 10 to 100 psi above the pressure within the chamber is applied ex-ternally to said chamber.
7. Apparatus as defined in claim 6 wherein said chamber is formed of a polymer of from 0.001 to 0.100 inches in thickness.
8. Apparatus as defined in claim 2 or 6 wherein said chamber is formed of an organic plastic having sufficiently high memory to be able to at least partially recover its surface shape after pressurization is relieved and forming means to assume a newly-shaped interface with the packing, on each pressurization of said diaphragm against said packing, minimizing fluid flow between the chamber wall and the porous mass packing.
9. Apparatus as defined in Claim 1 wherein said chamber comprises a thin layer of metallic foil.
10. Apparatus as defined in Claim 9 wherein said chamber is so construct-ed that it forms means to radially compress said mass when a pressure of about 10 to 1000 psi above the pressure within the chamber, is applied externally to said chamber.
11. Apparatus as defined in Claim 1 wherein said mass comprises a stationary-phase, liquid chromatography material.
12. Apparatus as defined in Claim 11 wherein said chamber has a diameter of less than about six inches.
13. Apparatus as defined in Claim 12 of the type comprising an elongate chamber wherein the wall of said chamber has been pre-stressed by pressure filling with said porous mass under heat so as to maintain said mass in a substantially uniform state of compression during shipment or use.
14. Apparatus as defined in Claim 13 wherein said porous mass of particles comprises the immobile phase component of a liquid chromatography packing material.
15. Apparatus as defined in Claim 14 wherein said chamber wall is formed of stainless steel.
16. Apparatus as defined in claim 14 wherein said chamber is formed of a metallic material and the wall of said chamber comprises, in contact with said porous particulate mass, a coating of a distensible organic material forming means to conform to the surface of said mass of particles and to reduce void volume also at the interface of said mass of particles with said chamber wall.
17. Apparatus as defined in claim 16 wherein said organic material is formed of polytetrafluoroethylene or polyethylene.
18. Apparatus as defined in claim 11, wherein said material of said mass comprises an immobile phase material forming means to differentially retard the passage of chemical compounds through said chamber and wherein the compression arrangement takes up any decrease in volume of said mass caused by said compression.
19. Apparatus as defined in claim 18 wherein said chamber has a dia-meter of less than about six inches.
20. A process for making an apparatus for chromatography of the type having a fluid inlet, a fluid outlet at ends of an elongate chamber there-between, said chamber being filled with a packed immobile porous chromato-graphic bed of particles adapted to be intimately contacted by fluid flowing through said chamber, the process comprising the steps of (1) placing particles for forming said bed into said chamber, and (2) arranging for radially compressing said bed by reducing the cross-sectional area of said elongate chamber, (3) whereby void volume associated with the packing of said particles is reduced.
21. A process as defined in claim 20 wherein void volume at the inter-face between said mass of particles and said chamber is reduced by providing a distensible interior wall surface on said chamber, the compression arrangement being such that the wall surface conforms to the exterior sur-face of said particulate mass and diminishes the volume of flow path be-tween said wall and said mass of particles.
22. A process as defined in Claim 20 wherein said radial compressing is arranged by (1) expanding the chamber (2) filling the chamber with said mass of particles, and then (3) shrinking the chamber.
23. A process as defined in Claim 22 wherein said chamber is formed of a metallic wall and said expanding step is carried out by heating the chamber and the shrinking step by cooling the chamber.
24. A process as defined in Claim 22 wherein said chamber is formed of a polymer and said expanding is achieved after preheating said polymer.
25. A process as defined in Claim 22 wherein said chamber is formed of a polymer and said expanding step is carried out by forming a pressure dif-ferential across said polymer and expanding it by means of said pressure dif-ferential without increasing the strain of said polymer beyond the elastic modulus of said polymer.
26. A process as defined in Claim 25 wherein a fluid is passed through said porous mass of particles to achieve an intimate contact between said fluid and said mass, and said compression arrangement exerts on said mass radial compression during passage of said fluid through said chamber.
27. A process as defined in Claim 26 wherein said radial compression is exerted on said mass by external application of pressure through an elongate wall of said chamber during passage of said fluid through said chamber.
28. A process as defined in Claim 25 wherein the compressive force ex-erted by said differential pressure is from 10 to 1000 psig.
29. A process as defined in Claim 28 wherein said particulate mass comprises an immobile-phase partitioning agent of the type used in liquid chromatography.
30. The process as defined in Claim 20 further comprising radially expanding said chamber from the normal radius thereof prior to said placing step, and wherein said arranging step comprises allowing said chamber to return to its normal radius.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US63830175A | 1975-12-08 | 1975-12-08 | |
US638,301 | 1991-01-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1101785A true CA1101785A (en) | 1981-05-26 |
Family
ID=24559468
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA266,277A Expired CA1101785A (en) | 1975-12-08 | 1976-11-22 | Radial compression of packed beds |
Country Status (7)
Country | Link |
---|---|
JP (1) | JPS5276091A (en) |
CA (1) | CA1101785A (en) |
DE (1) | DE2655650A1 (en) |
FR (1) | FR2334410A1 (en) |
GB (1) | GB1569700A (en) |
NL (1) | NL184705C (en) |
SE (2) | SE453437B (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2900344C2 (en) * | 1978-01-06 | 1986-09-25 | Waters Associates, Inc., Milford, Mass. | Chromatography column |
US4228007A (en) * | 1979-01-08 | 1980-10-14 | Waters Associates, Inc. | Chromatographic cartridge and holder |
EP0040663B1 (en) * | 1980-05-17 | 1986-09-17 | Vermögensverwaltungs-Kommanditgesellschaft Dr. Ing. Herbert Knauer & Co. GmbH & Cie. | Column closure |
DE3021366A1 (en) * | 1980-06-06 | 1981-12-17 | Merck Patent Gmbh, 6100 Darmstadt | SEPARATION COLUMN FOR THE LIQUID CHROMATOR GRAPHI |
FR2504818A1 (en) * | 1981-04-29 | 1982-11-05 | Elf Aquitaine | Chromatographic sepn. of materials in column - of large diameter employing porous flow-diffusing elements |
JP5977889B2 (en) * | 2013-06-11 | 2016-08-24 | 株式会社ルネッサンス・エナジー・インベストメント | Monolith porous column |
WO2017088948A1 (en) | 2015-11-25 | 2017-06-01 | Merck Patent Gmbh | Monolithic sorbents having a metal cladding |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB837363A (en) * | 1957-03-21 | 1960-06-15 | Lkb Produkter Fabriksaktiebola | Apparatus for the separation of substances dissolved in a liquid |
US3005514A (en) * | 1959-04-20 | 1961-10-24 | Cons Electrodynamics Corp | Fluid treating columns |
NL125713C (en) * | 1961-05-29 | 1900-01-01 | ||
US3440864A (en) * | 1966-10-03 | 1969-04-29 | Phoenix Precision Instr Co | Liquid chromatographic column |
NL6709298A (en) * | 1967-07-05 | 1969-01-07 | ||
FR2219797B1 (en) * | 1973-03-01 | 1978-03-03 | Roussel Uclaf |
-
1976
- 1976-11-22 CA CA266,277A patent/CA1101785A/en not_active Expired
- 1976-12-07 SE SE7613762A patent/SE453437B/en not_active IP Right Cessation
- 1976-12-07 NL NLAANVRAGE7613571,A patent/NL184705C/en not_active IP Right Cessation
- 1976-12-07 FR FR7636802A patent/FR2334410A1/en active Granted
- 1976-12-08 GB GB51254/76A patent/GB1569700A/en not_active Expired
- 1976-12-08 DE DE19762655650 patent/DE2655650A1/en active Granted
- 1976-12-08 JP JP51147578A patent/JPS5276091A/en active Granted
-
1982
- 1982-04-28 SE SE8202669A patent/SE450750B/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
SE7613762L (en) | 1977-06-09 |
FR2334410A1 (en) | 1977-07-08 |
SE8202669L (en) | 1982-04-28 |
SE453437B (en) | 1988-02-01 |
DE2655650A1 (en) | 1977-06-23 |
JPS5276091A (en) | 1977-06-25 |
GB1569700A (en) | 1980-06-18 |
FR2334410B1 (en) | 1981-12-24 |
DE2655650C2 (en) | 1988-08-11 |
SE450750B (en) | 1987-07-27 |
NL7613571A (en) | 1977-06-10 |
JPS62454B2 (en) | 1987-01-08 |
NL184705C (en) | 1989-10-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4250035A (en) | Radial compression of packed beds | |
Kennedy et al. | The performance of packings in high performance liquid chromatography (HPLC) I. Porous and surface layered supports | |
Kirkland | High-performance liquid chromatography with porous silica microspheres | |
Guiochon et al. | Consolidation of particle beds and packing of chromatographic columns | |
Martin et al. | Effects of high pressure in liquid chromatography | |
EP0609373B1 (en) | Column with macroporous polymer media | |
US4093550A (en) | Column for high pressure liquid chromatography | |
CA1101785A (en) | Radial compression of packed beds | |
CA1115551A (en) | Process for packing chromatographic columns | |
US20050224414A1 (en) | Chromatographic column and methods for controlling sorbent density | |
Podgornik et al. | Large-scale methacrylate monolithic columns: design and properties | |
Edam et al. | Hydrodynamic chromatography of macromolecules using polymer monolithic columns | |
JP4931584B2 (en) | Separator with integrated guard column | |
Guiochon et al. | Consolidation of the packing material in chromatographic columns under dynamic axial compression. I. Fundamental study | |
Rodrigues et al. | Bioseparations with permeable particles | |
Sarker et al. | Consolidation of the packing material in chromatographic columns under dynamic axial compression II. Consolidation and breakage of several packing materials | |
Godbille et al. | Description and Performance of an 8 cm id Column For Preparative Scale High Pressure Liquid-Solid Chromatography | |
Cramers et al. | Potentialities of micro-packed columns: Some applications in petroleum chemistry | |
CA1071112A (en) | Chromatography tube | |
Porsch | Some specific problems in the practice of preparative high-performance liquid chromatography | |
Tong et al. | Theoretical studies of the preparation of packed capillary columns for chromatography | |
JP2002536651A (en) | Terminal device for monolith chromatography column | |
US6348150B1 (en) | Permanently radially compressed column | |
Huckabee et al. | In‐column bonded phase polymerization for improved packing uniformity | |
Koh et al. | Effect of the column length on the characteristics of the packed bed and the column efficiency in a dynamic axial compression column |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MKEX | Expiry |