GB2078127A - Linear overpressured thin-layer chromatographic apparatus - Google Patents
Linear overpressured thin-layer chromatographic apparatus Download PDFInfo
- Publication number
- GB2078127A GB2078127A GB8116364A GB8116364A GB2078127A GB 2078127 A GB2078127 A GB 2078127A GB 8116364 A GB8116364 A GB 8116364A GB 8116364 A GB8116364 A GB 8116364A GB 2078127 A GB2078127 A GB 2078127A
- Authority
- GB
- United Kingdom
- Prior art keywords
- layer
- linear
- sorbent
- membrane
- overpressured
- 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.)
- Granted
Links
- 239000002594 sorbent Substances 0.000 claims abstract description 24
- 239000012528 membrane Substances 0.000 claims abstract description 13
- 210000002445 nipple Anatomy 0.000 abstract description 2
- 239000012530 fluid Substances 0.000 abstract 2
- 239000002904 solvent Substances 0.000 description 21
- 238000004587 chromatography analysis Methods 0.000 description 14
- 239000003480 eluent Substances 0.000 description 12
- 238000000926 separation method Methods 0.000 description 11
- 238000000034 method Methods 0.000 description 8
- 238000011161 development Methods 0.000 description 6
- 238000004440 column chromatography Methods 0.000 description 5
- 239000012071 phase Substances 0.000 description 5
- 230000002457 bidirectional effect Effects 0.000 description 4
- 239000007789 gas Substances 0.000 description 3
- 239000011877 solvent mixture Substances 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 229920005372 Plexiglas® Polymers 0.000 description 2
- 238000012899 de-mixing Methods 0.000 description 2
- 238000010828 elution Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- DDBREPKUVSBGFI-UHFFFAOYSA-N phenobarbital Chemical compound C=1C=CC=CC=1C1(CC)C(=O)NC(=O)NC1=O DDBREPKUVSBGFI-UHFFFAOYSA-N 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000013375 chromatographic separation Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000013016 damping Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000007792 gaseous phase Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000004809 thin layer chromatography Methods 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
- G01N30/90—Plate chromatography, e.g. thin layer or paper chromatography
-
- 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
- G01N30/90—Plate chromatography, e.g. thin layer or paper chromatography
- G01N30/91—Application of the sample
-
- 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
- G01N30/90—Plate chromatography, e.g. thin layer or paper chromatography
- G01N2030/906—Plate chromatography, e.g. thin layer or paper chromatography pressurised fluid phase
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)
Abstract
A linear overpressure thin layer chromatographic apparatus comprises a base plate 2 supporting a sorbent layer 1 over which a membrane 4 is fitted. The membrane 4 is externally pressurised by a fluid medium 10. A transparent cover plate 5 is fitted over the membrane 4, and there are sealed inlets 6, 7 passing through the cover plate 5 for the introduction of the mobile phase and the samples, whose progress may be visually detected through cover plate 5. The temperature of base plate 2 is controlled by fluid passed through nipples 3. <IMAGE>
Description
SPECIFICATION
Linear overpressured thin-layer
chromatographic apparatus
The invention relates to a linear overpressured
thin layer chromatographic apparatus operating
with a closed sorbent layer which is pressurised
(externally) by a resilient plate by pneumatic,
hydraulic or other means, wherein the
development temperature can be set to the
desired value and the development selected as
desired in length or width, one-way or two-way,
dry or wet, isocratic or gradient, one-dimensional
or two-dimensional, or for the application of the
so-called "overrunning" technique.
Overpressured layer chromatography is a
closed planar liquid chromatographic technique,
wherein the sorbent layer is completely sealed off
by a plate put under external pressure and the
solvent (mobile phase) is forced to flow among the
particles of the sorbent with the aid of a suitable
dispenser. (See Hungarian Patent No. 173,749.)
This latest embodiment of planar liquid
chromatography has several advantages in
comparison with "classic" or conventional layer
chromatography: short time required for
separation, better separation (resolution), low
solvent consumption; a possibility of speeding up
development by means of viscous solvent
mixtures; a possibility of visual evaluation;
applicability of aggressive reagents, etc.It may,
therefore, be stated that it combines the
advantages of overpressured layer
chromatography and the high-performance (high
velocity, high pressure) column chromatography.
There is, however, only one known
embodiment of overpressured thin layer
chromatographic apparatus: the so called "annular
or circular overpressured chamber" (TyihBk E.,
Mincsovics E., and Kalbsz H: J. Chromatog. 174,
75 (1979)) which is characterised in that the
apparatus (ultra-microchamber) is made of
"plexiglass" and one its plates, the lower plate,
receives a max. 200 x 200 mm, smeared or
industrially pre-treated sorbent layer-plate, either
after dropping the samples or, in the case of wet
running, without sample dropping; then a cover
plate, made of "plexiglass" is placed on the
sorbent layer and the following is incorporated
thereinto;
a) a manometer, b) pressurised sample
dispenser, c) a gas inlet aperture, d) an O-ring to clamp the synthetic resin foil, e) a synthetic membrane and f) an opening for introducing the solvent by means of a resilient pipe made of metal ,coil.
The two plates are suitably sealed together and
the gas pad or cushion is inflated with nitrogen
gas.
A common characteristic of the most widely
different variants known layer chromatographic
methods is that the relation between the distance
covered by the solvent (z, cm) and the time
required for it (t, sec.) can be described by a
quadratic equation: z2/7 = k, where k is a velocity constant. This also holds true for the liner and circular variants of high-performance liquid chromatography (HPLC), see Kaiser, R. E.: "Einfuehrung in die Hochleistungs-Diinnschicht- Chromatographie; Institute for Chromatography, Bad-Duerkheim, 1 976), as well as for running with overpressurised layer chromatographs of the annular variant (TyihBk et al., J.Chromatog. 174, 75, (1979) since in the latter case it-is in principle impossible to ensure constant solvent velocity along the radius of the circle.
A constant solvent velocity, or a linear solvent front are pre-conditions for a satisfactory layer chromatogram but they may only be achieved by a variant of the overpressured linear layerchromatograph wherein a wire of a platelet for the introduction of a solvent is placed in front of the point of entry of the solvent into the layer which is sealed at its edges or by a channel grooved into the sorbent layer. (Hungarian Patent Application, 6 Dex. 1979. Applicant: Chinoin Rt., Budapest.The title of the patent application is; Chromatographic layer plate for overpressured layer chomatographic apparatus.)
In linear overpressured chromatography the reflation between the distance covered (migrated) by the solvent (z cm.) and the time required (t sec.) is described by a linear equation: z/t = k, where k = velocity constant, thus this variant of overpressured layer chromatography creates conditions similar to those in column chromatographic conditions. This means that as regards quality a new chromatographic technique is presented.It also follows from this that of the two possible variants of overpressured layer chromatography, i.e. the circular and linear embodiments, the development of the latter is to be preferred, or is more justified, because it is there that an advance on the present state of art in respect of a more efficient separation can be expected.
Thus, the practical realization of overpressured linear layer chromatography requires suitably developed special sorbent plates (see Chinoin Rt.,
Budapest, Hungarian Patent Application of 6 Dec.
1979) and apparatus (chamber).
In the light of the published values of running time the further-developed linear apparatus, based on Hungarian Patent No. 173.749 (Tyihák and others, J. Chromatog. 191,293 (1980)) can only be used for runs over relatively short distances, although it follows from the basic law of the linear technique embodied in a linear equation (K = z/t) that the flow velocity of the solvent remains constant also over longer distances. Since as is known, the theoretical "plate-number" or "separation-number" introduced by Kaiser (Kaiser, R.E., Editor "Einfuerhrung in die Hochleistungs-DUnnschicht-Chromatographie, Bad Duerkheim, 1976) increases proportionally with the distance of the run, and so over longer distances (e.g. 30-100 cm) more efficient resolution than hitherto should be achievable.
It follows from the principle of overpressured layer chromatography that the chromatographic operations take place under the exclusion of solvent vapours similarly to column chromatography using dry packing. This frequently leads to the de-mixing or separationout of solvents from multicomponent solvent mixtures and therefore in liquid-solid (adsorption) overpressured layer chromatography to imperfect separation and to congestion or agglomeration of the materials to be separated at the boundaries of the separation zone. In such cases the disadvantageous separation could be counteracted by preconditioning with the solvent used with the sorbent, as in high-performance column chromatography. This kind of linear apparatus is, however, not known at the present.The evolution and application of a linear apparatus, which is also suitable for wet runs is further justified by the existing need for modelling high-performance column-chromatography and by the requirement for the simultaneous application of the two techniques for analytical and/or preparative purposes.
An aim of the invention is to eliminate the drawbacks described above and to satisfy the practical demand for a linear overpressured layer chromatograph suitable for the development of a closed, pneumatically, hydraulically or otherwise pressurised sorbent-layer which can be set to any desired, which is discretionally selectable to be long or wide, undirectional of bidirectional dry or wet, isocratic or gradient, one-dimension or twodimensional and applicable to the so-called "overrunning" technique.
The invention is based on the theoretically founded discovery that in linear overpressured thin layer chromatography the flow rate of the solvent remains constant over the full length of the layer, therefore runs over longer distances is justified and results in substantially more efficient separation than hitherto.
The invention is based on the recognition that the detrimental consequences of the separation or de-mixing into components of the solvent-mixture are eliminated analogously to high-performance column chromatography by preconditioning with a solvent, by dispensing or feeding the samples under pressure or after removal of the pressure.
This is also the basis of the modelling of highperformance column-chromatographic separation.
Furthermore, the invention is based on the recognition that the application of a sorbent layer with sealed or boundaries edges if so required, renders one or two-way running possible by using inlet apertures for the solvent built into the linear over-pressured layer chromatograph for variable operation according to the actual requirements.
Finally, the invention is based on the recognition that by setting the temperature of the sorbent-layer in the apparatus to a lower or higher degree than normal, better separation can be achieved than hitherto.
The solution according to the invention is, therefore, embodied in a linear overpressured layer-chromatographic apparatus (chamber), which is suitable for the application of discretionally selectably long or wide, one-way or two-way, dry or wet, isocratic and gradient, onedimensional or two-dimensional development or for the so called "over-running" technique and, at the same time, ensures the possibility of setting the temperature of the sorbent layer plate or running.The essence of the invention is that it utilizes the theoretically proved interrelation between the plate number, the separationnumber and the distance of the solvent migratipn in order to build apparatus suitable also for long runs as well as building into the apparatus a variable system of solvent introductions for wet elution, and a similarly variable sample dispensing system ensuring the possibility of a discretional selection of application. It is also an important feature of the invention that by means of a built-ip temperature control the temperature of the solvent and of the elution can be regulated.
According to the invention, a linear overpressured layer-chromatographic apparatus comprises:
1. A base plate, the dimensions of which are selected to suit the requirements of the new method regarding maintenance and control of the temperature of the sorbent layer plates;
2. A transparent, resilient damping plate which is provided with a gas cushion and is suitable for pressing down the sorbent layer, and the material of which is chemically resistant to solvents;
3. Capillary connectors for the introduction of eluents and samples.
The invention is further described purely by way of preferred embodiments illustrated in the accompanying drawings, wherein:
Figure 1 is a cross-section of the apparatus according to the invention,
Figure 2 is a cross-section of capillary connecting pieces for the introduction of eluents.
Figures 2a and 2b are respective plan views of further embodiments of the capillary connection pieces for the introduction of eluents, with Figures 2c and 2dshowing the capillary connection pieces of Figures 2a and 2b, respectively in cross-section,
Figure 3 is a cross-section of the sample dispenser,
Figures 4a, b, c and d illustrate various methods for the introduction of eluents and samples.
In Figure 1 a sorbent layer plate 1 is located on a thermostatically controlled base plate 2. Nipples 3 can be connected to ultra-thermostats to provide the temperature required for the chromatographic operation.
A membrane 4 for the clamping plate of the sorbent-layer is fastened to a strong, transparent synthetic resins or glass plate 5. Capillary inlet connectors 6 and 7, respectively for eluents and for samples are connected to the membrane 4.
The capillary connectors project to the external space of surroundings via seals 8 in the transparent strong plate 5.
The base plate 2 and the clamping plate 5 are tightly clamped together by means of a special closure 9. A high-pressure liquid or gaseous phase 10 is introduced between the membrane 4 and the transparent plate 5 via a valve 11. A manometer 12 indicates the prevailing pressure conditions. The sorbent layer plate 1 is directly sealed by the pressure exerted by the elastic pad or cushion developed on one side of the clamping plate 5. The degree of clamping depends on the magnitude of the pressure applied.
The seals 8 of the capillary inlet connectors permit movement of membrane 4 and/or of the capillary connectors 6, 7 in such a way that the fluid-tightness of the space 10 under pressure is assured.
As shown in Figure 2, the capillary connector 6 for the introduction of the mobile phase is connected to the membrane 4 by means of a conical seal. The tightness of this seal is ensured by means of a conical shim 13 and a threaded nut 14. The mobile phase may be introduced via a channel 1 5 formed in the sorbent layer, or via a channel 1 8 formed by the spacing wire 17 placed on the sorbent layer, the plate strip and the clamped membrane 4 (Figure 2a to 2d).
Initially the channel 1 5 and the sorbent layer 1 behind it fill up. Thereafter, as the pressure increases, linear flow indicated by arrows is set up in the sorbent layer, the edges of which are sealed by impregnation 19.
In Figure 3 the capillary connector 7 for the introduction of samples is laid directly on the sorbent layer 1. The sample 20 flows into the sorbent-layer 1 by overpressure. The sample can be introduced by wetting the sorbent layer by the flow of the eluent, or without wetting into a dry sorbent-layer. The magnitude of the overpressure for the sample dispensing is determined by the magnitude of the pressure in the cushion 10 which presses down the sorbent-layer 1, by the particle size of the sorbent and by the viscosity conditions.
Figures 4a to 4d show various embodiments of the eluent and sample-taking in the linear overpressured layer chromatographic apparatus, according to the invention, offering the possibility of the realization of different ways of separation.
a.) One-way runs with pre-loaded samples. The mobile phase is introduced through the capillary connector 6 via the channel 1 5 and sets the components of the pre-loaded samples 20 into a one-way linear motion (Figure 4a).
b.) Two-way runs with pre-loaded samples. The phase or eluent is introduced through the capillary connector 6 via the channel 1 5 and sets the greater number of pre-loaded samples 20 arranged in two rows into a two-way (bidirectional) linear motion (Figure 4b).
c.) One-way running with pressurized sample dispensing.
The eluent is introduced through the capillary connector 6 via the channel 1 5 and wets or elutriates the sorbent-layer. The samples are introduced through the capillary connector 7. The flow of eluent sets the samples into a one-way (unidirectional) linear motion (Figure 4c).
d.) Two-way (bidirectional) running with pressurized sample dispensing. The elutriates the sorbent-layer via the channel 1 5 in two directions.
Through a greater number of capiiary connectors 7 arranged in two rows a plurality of samples are introduced. The flow of the eluent sets the samples into a bidirectional linear motion. (Figure 4d.)
The front of the eluent can be observed through the transparent clamping plate. In the case of a coloured compound or mixture the motion of the sample may be observed directly. In the case of a colourless sample coloured tracing additives may be used to make the visual observation possible.
The evaluation of the separation is carried out with the aid of the methods used in traditional layer chromatography.
Claims (2)
1. Linear overpressured layer chromatographic apparatus comprising a base plate to support a sorbent layer, a cover plate fastenable to the base plate and fitted with a membrane for resiliently clamping down the sorbent layer, means for controlling the introduction of a pressurising between the cover plate and the membrane; and the cover plate is provided with at least one inlet for the mobile phase and at least one sample inlet sealedly passed through the membrane plate.
2. Apparatus according to claim 1 substantially as herein described with reference to and as shown in the accompanying drawings.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU801388A HU182141B (en) | 1980-06-03 | 1980-06-03 | Linear layer-chromatographic apparatus of overpressure |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2078127A true GB2078127A (en) | 1982-01-06 |
GB2078127B GB2078127B (en) | 1984-01-18 |
Family
ID=10954239
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8116364A Expired GB2078127B (en) | 1980-06-03 | 1981-05-28 | Linear overpressured thin-layer chromatographic apparatus |
Country Status (12)
Country | Link |
---|---|
JP (1) | JPS5748654A (en) |
CH (1) | CH654218A5 (en) |
CS (1) | CS235089B2 (en) |
DD (1) | DD159465A5 (en) |
DE (1) | DE3118665A1 (en) |
FR (1) | FR2483248A1 (en) |
GB (1) | GB2078127B (en) |
HU (1) | HU182141B (en) |
IT (1) | IT1136635B (en) |
PL (1) | PL128659B1 (en) |
SE (1) | SE449055B (en) |
SU (1) | SU997618A3 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2173125A (en) * | 1985-04-04 | 1986-10-08 | Mueszeripari Muevek Lab | Overpressured thin layer chromatography |
FR2843198A1 (en) * | 2002-08-02 | 2004-02-06 | Bionisis Sa | DEVICE FOR SEPARATING CONSTITUENTS OF SAMPLES BY PRESSURE LIQUID CHROMATOGRAHY |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61239161A (en) * | 1985-04-16 | 1986-10-24 | ラボル ミセリパリ ミベク | Device for overpressure thin-layer chromatography |
JP2001328425A (en) | 2000-05-19 | 2001-11-27 | Nippon Pop Rivets & Fasteners Ltd | Molding installing device |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4134730A (en) * | 1977-09-20 | 1979-01-16 | Quame Babington A | Spotting systems and methods pertaining thereto |
DE2921334A1 (en) * | 1978-05-25 | 1979-12-06 | Fenimore David Clarke | Transferring specimens onto thin layer chromatography substrate - after evaporation of solvent vehicle on transfer sheet, giving a conc. spot |
-
1980
- 1980-06-03 HU HU801388A patent/HU182141B/en not_active IP Right Cessation
-
1981
- 1981-05-12 DE DE19813118665 patent/DE3118665A1/en not_active Withdrawn
- 1981-05-25 SE SE8103285A patent/SE449055B/en not_active IP Right Cessation
- 1981-05-26 CH CH3431/81A patent/CH654218A5/en not_active IP Right Cessation
- 1981-05-28 GB GB8116364A patent/GB2078127B/en not_active Expired
- 1981-05-29 CS CS813969A patent/CS235089B2/en unknown
- 1981-05-29 JP JP56081190A patent/JPS5748654A/en active Pending
- 1981-06-02 FR FR8110885A patent/FR2483248A1/en active Pending
- 1981-06-02 IT IT22104/81A patent/IT1136635B/en active
- 1981-06-03 DD DD81230550A patent/DD159465A5/en not_active IP Right Cessation
- 1981-06-03 PL PL1981231469A patent/PL128659B1/en unknown
- 1981-06-03 SU SU813291149A patent/SU997618A3/en active
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2173125A (en) * | 1985-04-04 | 1986-10-08 | Mueszeripari Muevek Lab | Overpressured thin layer chromatography |
GB2173125B (en) * | 1985-04-04 | 1989-04-19 | Mueszeripari Muevek Lab | Apparatus for overpressured thin-layer chromatographic technique |
FR2843198A1 (en) * | 2002-08-02 | 2004-02-06 | Bionisis Sa | DEVICE FOR SEPARATING CONSTITUENTS OF SAMPLES BY PRESSURE LIQUID CHROMATOGRAHY |
WO2004017064A1 (en) * | 2002-08-02 | 2004-02-26 | Bionisis S.A. | Device for separating sample components by liquid chromatography under pressure |
CN100350245C (en) * | 2002-08-02 | 2007-11-21 | 比奥尼西斯股份有限公司 | Device for separating sample components by liquid chromatography under pressure |
Also Published As
Publication number | Publication date |
---|---|
SU997618A3 (en) | 1983-02-15 |
DD159465A5 (en) | 1983-03-09 |
HU182141B (en) | 1983-12-28 |
GB2078127B (en) | 1984-01-18 |
CH654218A5 (en) | 1986-02-14 |
PL128659B1 (en) | 1984-02-29 |
CS235089B2 (en) | 1985-04-16 |
SE8103285L (en) | 1981-12-04 |
DE3118665A1 (en) | 1982-02-04 |
PL231469A1 (en) | 1982-03-29 |
SE449055B (en) | 1987-04-06 |
FR2483248A1 (en) | 1981-12-04 |
IT8122104A0 (en) | 1981-06-02 |
JPS5748654A (en) | 1982-03-20 |
IT1136635B (en) | 1986-09-03 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19920528 |