AU2003255792A1 - Method and apparatus for pumping and diluting a sample - Google Patents
Method and apparatus for pumping and diluting a sample Download PDFInfo
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- AU2003255792A1 AU2003255792A1 AU2003255792A AU2003255792A AU2003255792A1 AU 2003255792 A1 AU2003255792 A1 AU 2003255792A1 AU 2003255792 A AU2003255792 A AU 2003255792A AU 2003255792 A AU2003255792 A AU 2003255792A AU 2003255792 A1 AU2003255792 A1 AU 2003255792A1
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- 238000000034 method Methods 0.000 title claims description 39
- 238000005086 pumping Methods 0.000 title claims description 39
- 238000007865 diluting Methods 0.000 title claims description 9
- 239000000523 sample Substances 0.000 claims description 217
- 239000012530 fluid Substances 0.000 claims description 125
- 239000003085 diluting agent Substances 0.000 claims description 70
- 238000010790 dilution Methods 0.000 claims description 59
- 239000012895 dilution Substances 0.000 claims description 59
- 238000004458 analytical method Methods 0.000 claims description 46
- 238000002156 mixing Methods 0.000 claims description 45
- 238000004891 communication Methods 0.000 claims description 29
- 239000012470 diluted sample Substances 0.000 claims description 22
- 239000002699 waste material Substances 0.000 claims description 22
- 239000000126 substance Substances 0.000 claims description 8
- 238000011109 contamination Methods 0.000 claims description 6
- 238000006073 displacement reaction Methods 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 230000004044 response Effects 0.000 claims description 3
- 238000004590 computer program Methods 0.000 claims 2
- 238000012544 monitoring process Methods 0.000 claims 1
- 239000013026 undiluted sample Substances 0.000 claims 1
- 238000011144 upstream manufacturing Methods 0.000 claims 1
- 230000002572 peristaltic effect Effects 0.000 description 12
- 238000012360 testing method Methods 0.000 description 12
- 229910052738 indium Inorganic materials 0.000 description 9
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 9
- 239000011159 matrix material Substances 0.000 description 9
- 229910052703 rhodium Inorganic materials 0.000 description 7
- 239000010948 rhodium Substances 0.000 description 7
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 230000008901 benefit Effects 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000012488 sample solution Substances 0.000 description 5
- 239000012491 analyte Substances 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 3
- 230000008602 contraction Effects 0.000 description 3
- 238000012421 spiking Methods 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 230000001627 detrimental effect Effects 0.000 description 2
- 238000004949 mass spectrometry Methods 0.000 description 2
- 230000003446 memory effect Effects 0.000 description 2
- 235000013619 trace mineral Nutrition 0.000 description 2
- 239000011573 trace mineral Substances 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000012864 cross contamination Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000010339 dilation Effects 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 238000009616 inductively coupled plasma Methods 0.000 description 1
- 238000000752 ionisation method Methods 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 239000012858 resilient material Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- -1 urine Substances 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/10—Devices for transferring samples or any liquids to, in, or from, the analysis apparatus, e.g. suction devices, injection devices
- G01N35/1095—Devices for transferring samples or any liquids to, in, or from, the analysis apparatus, e.g. suction devices, injection devices for supplying the samples to flow-through analysers
- G01N35/1097—Devices for transferring samples or any liquids to, in, or from, the analysis apparatus, e.g. suction devices, injection devices for supplying the samples to flow-through analysers characterised by the valves
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N1/00—Sampling; Preparing specimens for investigation
- G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
- G01N1/38—Diluting, dispersing or mixing samples
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/08—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor using a stream of discrete samples flowing along a tube system, e.g. flow injection analysis
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)
- Sampling And Sample Adjustment (AREA)
- Automatic Analysis And Handling Materials Therefor (AREA)
- Other Investigation Or Analysis Of Materials By Electrical Means (AREA)
Description
WO2004/017045 PCT/GB2003/003564 METHOD AND APPARATUS FOR PUMPING AND DILUTING A SAMPLE Field of the Invention This invention relates to a method and apparatus for 5 pumping a sample to analysis equipment and diluting the sample before it is analysed, or for any other reason. The invention is described herein with reference to liquid samples which require dilution before they are analysed in a mass spectrometer. However, the invention is 10 not limited to liquid samples or mass spectroscopy and can equally apply to dissolved or suspended samples and any other test or analysis equipment. Description of the Related Art 15 Analysis equipment for analysing trace elements in liquids have a limited capability of measuring samples which have relatively high levels of dissolved solid material, or matrix (such as CaCO 3 or dissolved salts in water, or the like). The trace elements of interest to the user are often 20 only a few parts per billion, or lower, whilst the matrix can be many parts per million, or higher. Such high levels of matrix can have undesirable effects on the analytical equipment, for example, materials can be deposited on orifices, glassware and ion optical elements. It is, 25 therefore, necessary to dilute the sample prior to analysis. Inductively coupled plasma mass spectrometers (ICP-MS) typically require a total dissolved solid level of less than 2000mg/1 to avoid such deleterious effects. The dissolved solids can become deposited on components within the 30 instrument, for example on the cones which sample the plasma and skim off a portion of the supersonic jet, thus significantly reducing the reliability of the test result WO2004/017045 PCT/GB2003/003564 -2 and the results of any other subsequent test. If deposition of materials occurs, the instrument has to be thoroughly cleaned before accurate testing can resume. Test laboratories are often required to analyse many 5 samples quickly where the matrix content of each sample varies widely. Typically, the user would wish to dilute each sample by a certain amount to determine the analytes present in each sample, and whether the sample can be analysed undiluted. If dilution is required, this initial 10 test provides an indication of the dilution factor necessary to bring the total dissolved solids down to a level tolerated by the instrument. Such manual intervention is too cumbersome, time consuming and costly if many samples per day require 15 analysis. Presently, samples which introduce too great a loading of dissolved solids for the instrument to cope with are re-analysed once the analyser has been cleaned. Analysis must stop for cleaning, and samples inadvertently analysed after contamination of the analyser must be re 20 analysed. This requires considerable operator intervention. Such a limit to the throughput of samples is undesirable and operator intervention is costly. Automated dilution systems have been used previously and, referring to figure 1, such an automated system 10 25 known in the art is shown in highly schematic form. A sample 12 is drawn from a container by a sample pump 14 to a mixing tube 16. Similarly, a diluent 18 is drawn by a diluent pump 20 to the mixing tube 16 from a separate diluent container. The sample is diluted in the mixing tube 30 where it is completely mixed with diluent. An instrument pump 22 draws the diluted sample from the mixing tube and into the instrument or analyser, not shown in figure 1.
WO2004/017045 PCT/GB2003/003564 - 3 Both the sample and diluent pumps have to be able to maintain accurate flow rates to ensure the sample is diluted precisely. If the dilution is not maintained to a known level and within a relatively tight tolerance, the accuracy 5 of the analysis results may be unacceptable. Likewise, the instrument flow must be maintained at an accurate flow rate to ensure the diluted sample is pumped to the analyser's input at a known, controllable rate. Thus, all the pumps (and their associated flow rates) need to be controlled 10 accurately to maintain accurate test results. Presently, peristaltic pumps are used to pump the sample, diluent and diluted sample through the dilution system. Typically, dilutions ratios of 50:1 of diluent to sample are used for mass spectroscopy. Hence, the diluent 15 pump rate is typically fifty times greater than the sample pump rate. Peristaltic pumps have a limited range of flow rates and the sample and diluent pumps often operate at the extremes of their flow rate range. Also, the limited flow rate for peristaltic pumps limits the dilution factor by 20 which the sample can be diluted; the maximum dilution occurring whilst the diluent pump operates at a maximum flow rate and the sample pump operates at a minimum flow rate. The rate at which the diluted sample should enter the instrument (not shown) depends on the type of instrument 25 being used but is relatively low and typically a few millilitres per minute. If this rate is exceeded the instrument will become swamped with diluted sample which will cause problems in the spectrometer and have a detrimental effect on the analysis results. Typically, the 30 combined flow rates of the sample and diluent pumps far exceeds the instrument pump flow rate. This is because all the pumps have relatively similar ranges of flow rates, and WO2004/017045 PCT/GB2003/003564 -4 at dilution factors greater than ten, for example, the diluent pump 20 must operate at a high flow rate. This high flow rate typically exceeds the flow accepted by the analysis instrument. It is, therefore, necessary to 5 provide a waste outlet 24 to prevent build up of pressure in the system; excess diluted sample not pumped to the instrument flows to a waste container 26. At high dilution factors, the solution flowing to waste can exceed the flow entering the instrument by a factor of fifty. Materials in 10 the waste container are discarded and, since the high quality diluent necessary for accurate test results is relatively expensive, this wastage is an additional economic burden on test laboratories. Another automated pumping system 28 known in the art is 15 shown in figure 2 in highly schematic form. Sample 29 is pumped along a first pipe 30 by a syringe pump 31 to fill the syringe (not shown). A valve 32 is closed to prevent fluid entering the syringe from the pump discharge pipe 33. When the pump is charged with an appropriate amount of 20 sample, the valve is opened and the syringe plunger driven at a constant rate to provide a flow of sample along pipe 33 in the general direction indicated by arrow Z. A one way valve in the pump (not shown) prevents the sample from flowing back to the container 29 during the phase when the 25 sample flows along pipe 33. A mixing region 34 of the pipe is defined by a second pipe 35 adjoining pipe 33 in a generally "T" or "Y" shaped configuration. As solution is aspirated by the instrument pump system (for example, a nebuliser), an uncontrolled 30 pressure drop is produced in pipe 35. This causes an uncontrolled flow of solution along pipe 33' from the mixing region 34. This flow rate is a combination of a controlled WO2004/017045 PCT/GB2003/003564 - 5 flow of solution from the syringe pump, and an uncontrolled flow of diluent along pipe 35. The inability to control the flow of diluent results in an uncontrolled dilution factor. There is no instrument pump to pump the diluted sample to 5 the analyser in this arrangement. Problems arise with systems which rely on this arrangement. For instance, there are limits to the dilution factor this system can provide, especially if the analyser requires the diluted sample to be pumped at a specific rate. 10 This problem could be overcome by providing an instrument pump and pressure relief system similar to that shown in figure 1. However, the problems associated with the system in figure 1 now become prevalent with the system, for example, diluent wastage. 15 Pumping systems known in the art are disclosed in US 4,245,509 (Instrumentation Laboratory Inc.) and US 5,007,297 (Pacific Scientific Company). Furthermore, contamination of the pump parts exposed to the sample during operation can cause subsequent samples to 20 become contaminated, thus resulting in inaccurate analysis results. This so called "memory effect" problem is particularly troublesome with highly sensitive analysis instruments. As test instruments become more sensitive, this problem further increases. (For example, we have found this 25 problem has very little effect on analysis results when samples are tested using the relatively insensitive atomic absorption analysis instruments, but can be problematic when samples are tested using highly sensitive ICP-MS analysis tools). 30 Also, certain fluids can damage pump components. Such damaged components can lead to inaccurate flow rates, or WO2004/017045 PCT/GB2003/003564 - 6 more seriously, render the pump unusable without lengthy repair or regular servicing. At present, peristaltic pumps are used; the liquid being pumped is only in contact with the tubing in such 5 pumps (which can be made of resilient material). However, peristaltic pumps have inadequate flow rate range and accuracy to dispense a sample solution at a sufficiently low flow rate to avoid discharging qualities of fluid to waste, as previously described. Furthermore, the use of 10 peristaltic pumps limits the dilution factor achievable, because of their limited effective flow rate range. Summary of The Invention It is an aim of the present invention to ameliorate the 15 problems associated with the prior art. More precisely, there is provided a pump apparatus for pumping a sample to an analyser for analysis, comprising; a first pump arranged to pump the sample into a buffer region at a first flow rate, and a second pump arranged 20 subsequently to pump a second fluid into said buffer region at a second flow rate to cause at least a portion of the sample to be displaced from the buffer region to the analyser, said second pump being operable so that the second flow rate is more accurately controllable than the first 25 flow rate. Advantageously, the second pump means for pumping the second fluid into the buffer region is isolated from the sample such that it does not come into contact with the sample and therefore overcomes the memory effect problem. 30 Furthermore, because the second pump's flow rate can be controlled with a relatively high degree of accuracy, subsequent dilution of the sample is achievable to higher WO2004/017045 PCT/GB2003/003564 -7 levels and which have less effect on analysis results than with prior art systems, and which we have found are necessary for relatively accurate analysis equipment, such as ICP-MS for example. 5 Embodiments of the invention may also comprise a flow switching means moveable between a first and second position, the flow switching means being so arranged that;(a) when the switching means is in the first position, the buffer region is in fluid communication with the second 10 pump, and (b) when the switching means is in the second position, a first buffer region port is in communication with the outlet conduit, and a second buffer region port is in fluid communication with the first pump. Embodiments of the invention can also comprise a waste 15 conduit so arranged that, when the switching means is in the first position, the buffer region is also in fluid communication with the waste conduit. Embodiments of the invention may also comprise, when the switching means is in the second position, the waste 20 conduit is in fluid communication with the second pump, the second pump can be being arranged to pump a flush agent. Embodiments of the invention can further comprise, when the switching means is in the first position, the first pump is in fluid communication with the outlet 25 conduit, so that the second fluid can be pumped into the outlet conduit for displacement of the sample fluid or second fluid therein. Advantageously, embodiments further include a mixing region for mixing the sample with a diluting agent, and a 30 third pump means for pumping diluted sample from the mixing region to the analyser, wherein, the mixing region is disposed between the outlet pipe and the analyser.
WO2004/017045 PCT/GB2003/003564 There is further provided a method for pumping a sample fluid for analysis to an analysis instrument using a pumping system comprising, a buffer region for storing the sample fluid, the buffer region being arranged with at least two 5 ports, the method comprising, pumping a second fluid into the sample fluid buffer region through a first port, using a first pump means, thereby displacing the sample fluid therein to the analyser. Advantageously, when the system further comprises a 10 second pump means, and an outlet conduit arranged for flow of the sample fluid and/or fluid to the analyser, the method may also comprise pumping the sample into the buffer region using the second pump means. Advantageously, when the system further comprises a 15 flow switching means moveable between a first and second position so arranged that; (a) when the switching means is in the first position, the buffer region is in fluid communication with the second pump, and (b) when the switching means is in the second position, a first buffer 20 region port is in communication with the outlet conduit, and a second buffer region port is in fluid communication with the first pump; the method further provides, pumping the sample into the buffer when the flow switching means is in the first position using the second pump, switching the flow 25 switching means to the second position, and pumping the second fluid into the buffer region using the first pump for displacement of the sample therein. The invention yet further provides a method of preventing contamination of a first pump means with a 30 sample, the method comprising; disposing the sample in an intermediary region using a second pump, displacing the sample from the intermediary region by pumping a second WO2004/017045 PCT/GB2003/003564
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fluid into said intermediary region using the first pump means. A main advantage of the present invention broadly reside in a pumping or dilution system in which the sample 5 is pumped to the analysis instrument at a flow rate determined by a highly accurate pump, without exposing that pump to the sample. This can reduce the likelihood of the pump becoming damaged or contaminated by the sample. Also, the accurate flow rate may be required for relatively high 10 precision dilution of the sample. Embodiments of the present invention also have the advantage of providing a pump/dilution system and method which is more easily controlled and to better accuracy levels of flow rate and dilution factor. Also, virtually no 15 diluent is wasted during normal operation. A controller can advantageously be used to control the second and third pump flow rates. A dilution factor equal to the ratio of fourth to second flow rates can easily be controlled by adjusting the second and/or third pump flow rates accordingly. Control 20 of the dilution factor can occur in substantially real time in response to data from the analysis equipment. Also, the components of the pump used to provide accurate, low level flow of the sample are not exposed to potentially damaging corrosive, chemical attack, or wear caused by suspended 25 solids in the sample. Sample solution does not enter the second pump. Embodiments of the invention have further advantages of substantially reducing the operator intervention, and increase the sample throughput rate. The embodiments aim to 30 provide automated dilution of the sample at a consistent and safe level before the sample is introduced into the analyser. The rate of sample throughput can be WO2004/017045 PCT/GB2003/003564 - 10 substantially increased. Dilution of the sample to a safe level also has the advantage of allowing the required precision of analysis to be carried out on trace levels within the sample by automatic dilution of the sample. The 5 sample throughput can also be increased by a relatively rapid introduction of new (or different) sample solutions up to the buffer by controlling the flow rate of the sample uptake. The cost of diluting samples can be reduced by reducing the amount of diluent used by the dilution system; 10 only the volume of diluent required to dilute the sample to a required safe level can be consumed and little or no diluent is wasted. By 'safe level', we mean a dilution factor necessary to avoid contamination of the analysis instrumentation. 15 Detailed Description of An Embodiment An embodiment of the present invention will now be described, by way of example, with reference to the accompanying drawings, in which: 20 Figure 1 is a schematic diagram of a pump system known in the art and described above; Figure 2 is a schematic diagram of a pump system known in the art and described above; Figure 3 is a schematic diagram of a pump system 25 embodying the present invention with a switch in a first position; and Figure 4 is a schematic diagram of the switch of figure 3 shown in a second position. Referring to Figure 3, a pump system 50 embodying the 30 present invention is shown in schematic form. A sample 52 to be analysed is drawn from a container by an automatic sampler 54 along a first, or sample uptake pipe 56 to a WO2004/017045 PCT/GB2003/003564 - 11 valve, or pipe flow switch 58. The automatic sampler used in this embodiment is well known in the art and comprises a pump (not shown) and a probe 60. The probe is moveable to be inserted into a fluid in a container placed underneath the 5 probe. Different containers can be placed on a carrousel (not shown) so that different samples or a washing agent 62 can be drawn into the pump system via the probe and automatic sampler pump. The switch 58 comprises six input/output ports, A, B, 10 C, D, E and F, and three internal pipes or conduits which each join one port with another. The switch is movable between two positions so that the flow of fluid from one pipe to another pipe can be switched from that pipe to a different pipe when the switch is moved. The switch is shown 15 in a first position in figure 3 and a second position in figure 4. In an initial, or sample uptake phase, whilst the sample is being drawn in to the system, the switch is configured as shown in figure 3 (first position), so that 20 port A is connected to F, B is connected to C, and D is connected to E. Thus, fluid can flow between pipes connected to ports A and F, B and C, and D and E respectively. A second, or sample storage pipe 64 connects port E with port B. Thus, in the sample uptake phase, the sample is 25 pumped through the switch port D, out the switch port E and into the second pipe 64; the ports act to allow fluid to flow through the port and into or out of a pipe, conduit or chamber attached to the port. Any fluid already in the second pipe is displaced by the sample entering the second 30 pipe into the switch via port B. A third, or waste pipe 66 is connected to port C of the switch (which is, in turn, connected to port B in the sample uptake phase) and a waste WO 2004/017045 PCT/GB2003/003564 - 12 unit 68. Thus, fluid displaced from the second pipe is pushed through the switch (via ports B and C), along the third pipe to a drain, or waste unit. The second pipe 64 has sufficient volume to contain or 5 store enough sample fluid required for testing. Typically, for ICP-MS applications, a volume of 1-10 ml is required for a single sample to obtain sufficient analysis results, although this volume depends on a dilution factor of the sample entering the mass spectrometer. The automatic sampler 10 is controlled to draw a volume of sample into the second pipe from the sample container which exceeds the combined volume of the pipe 56, the second pipe 64 and any volume occupied by fluid with the switch 58. This ensures the sample completely fills the second pipe. Thus, any fluid 15 within the second pipe, prior to the sample being drawn into the pipe, is flushed out of the second pipe 64. Also, the interface between the sample and any fluid which occupied the second pipe prior to sample uptake is now in the third pipe 66 when the sample update is complete. 20 A second, sample pump phase of the pump system shall now be described in which the sample is pumped to the instrument for analysis. Once the second pipe 64 has been filled with sufficient sample, the automatic sampler stops pumping sample from the container. The switch is switched to 25 the second position shown in figure 4, where Port A is connected to B, C to D, and E to F. This switch configuration now connects a fourth, or system pump pipe 70 to an end on the second pipe, via switch ports A and B. The end of the second pipe connected to port B is distal from 30 the automatic sampler, and is the end through which fluid in that pipe passes to the waste outlet (as previously WO2004/017045 PCT/GB2003/003564 - 13 described). Thus, this end contains sample fluid, since all of the second pipe has been filed with sample. A first, system pump 72 is now operated to pump a fluid, or diluent 73 from a container 74 into port A. 5 Preferably, this fluid is suitable for diluting the sample and should have an extremely high level purity. The fluid is pumped into the switch (port A), and thence into the distal end of the second pipe (port B) by pump 72. In this way, the sample in the second pipe 64 is displaced from the second 10 pipe, through switch port E, out of switch port F and into a fifth, or switch outlet pipe 76. The rate of flow (litres per minute) along the fifth pipe is equal to the rate of flow of pump fluid along the fourth pipe 70. Of course, this assumes the fluids are incompressible and that the 15 pipes do not expand during normal operations. The sampler probe is, at the same time, now switched so that another fluid 62 can be pumped into pipe 56, through switch 58 and along the second pipe 66, via ports D,E,B and C. Preferably, the another fluid is suitable to wash, or 20 flush out sample fluid in pipe 56 and the probe thereby cleaning these components in readiness for the next sample by flushing sample solution to the waste container 68 through pipe 66. The first pipe is now in communication with the third pipe 66, via switch ports D and C (since the 25 switch is in the second position), so that the wash fluid flushes sample from pipe 56 and into waste pipe 66 to the waste disposal 68. The flow rate of the sample passing along the fifth pipe 76 is governed by the sample pump 72 to Flow 1. The 30 sample enters a mixing region 78 at the end of fifth pipe where it is mixed with a diluent 80. At the mixing region 78, the fifth pipe 76 is joined to a sixth, or sample WO2004/017045 PCT/GB2003/003564 - 14 diluent pipe 82 to form a single, seventh, or instrument input pipe 84. This mixer is a "Y" or "T" configured junction in the tubing or pipes. A more complex shape or configuration could also be used to encourage mixing of 5 sample and diluent solutions. The exit of the mixing region comprises a single pipe 84 disposed between the mixing region and a second pump 86 which pumps fluid from the mixing section to an instrument (not shown) for analysis. Mixing of the sample and diluent to form a diluted 10 sample takes place at the interface of the fifth, sixth and seventh pipes 76, 82 and 84 respectively. Additional mixing may also occur for some length along the seventh pipe from the mixer to the analyser (not shown) but mixing should be complete before the diluted sample enters the analyser. 15 Mixing occurs as a function of the turbulent flow of the sample and diluent at the junction and along the fifth pipe, and also by diffusion of the two fluids. In this embodiment, mixing may also occur as the fluid passes through the second pump 86. 20 The first, or sample pump 72 is preferably a piston type pump, similar to the milliGAT pump head supplied by Global FIA Inc. (disclosed in US6,079,313). This type of pump allows a much greater range of flow rates, compared to peristaltic pumps, for instance, and can operate to 25 continuously pump relatively small volumes of sample at a constant, or varying flow rate, as desired. In particular, it is capable of delivering very low flow rates at high levels of accuracy and precision. Furthermore, this piston pump system does not suffer the disadvantages associated 30 with the prior art pump systems described previously. The second, or instrument pump may be the same type as the first pump, or, if appropriate, may be a peristaltic pump.
WO 2004/017045 PCT/GB2003/003564 - 15 Typically, the automatic sampler pump is also a peristaltic pump. The use of such a pump for sample pumping has the advantage of the sample remaining in the pump tubing and thus, the sample does not damage any pump components. 5 However, peristaltic pumps can not dispense fluid at low volume rates (typically micro-litres per minute), at the precision required and with near pulse-less delivery. Peristaltic pumps are therefore limited to relatively high volume flow rates (millilitres per minute) and at relatively 10 inaccurate and imprecise pumping rates. Such peristaltic pumps are suitable for the application described herein where the sample store can be filled rapidly and the pumps do not suffer corrosion or mechanical damage. Of course, such pumps are not suitable for pumping the sample to the 15 mixer 78 because they do not have the same amount of controllability in consistent flow rates which are required to maintain accurate dilution factors of the sample. In other words, the flow rate of these unsuitable pumps varies, or pulses to an extent which can be detrimental to the 20 consistency of the diluted sample. The diluent 80 is drawn from a diluent container container 81, up the sixth pipe 82 to the mixing section 78 where it mixes with the sample, and hence dilutes the sample. The end of the sixth pipe at which the diluent 25 enters the system is completely submersed in the diluent to ensure air does not enter the system. The flow from the mixer to the instrument of the diluted sample is accurately controlled by the second pump 86 at Flow 3. Thus, when Flow 1 < Flow 3, the diluent is drawn along the sixth pipe 82 to 30 the mixer at a flow rate Flow 2, following the equation Flow 1 + Flow 2 = Flow 3 ; WO2004/017045 PCT/GB2003/003564 - 16 assuming the liquids in the pipes are non-compressible. (The flow can be measured in litres per minute). Preferably, Flow 3 is kept constant by the second pump 5 86, hence the rate of arrival of diluted sample of the instrument is constant. Varying the flow rate of the first pump therefore changes the dilution factor D by which the sample is diluted, where 10 D = Flow 2 / Flow I ,or D = (Flow 3 / Flow 1) - 1. So, from the equations above and assuming Flow 3 is constant, a decrease in the first pump's flow rate (Flow 1) 15 increases the diluent flow to the mixer section, and hence increases the dilution factor D. An example of how the pump system embodying the invention can operate with an ICP-MS instrument is now provided. During operation, all samples are routinely 20 diluted by a discrete dilution factor D, before the sample is analysed. D, is initially set to a relatively high level so that the sample is diluted to such an extent that any dissolved solids (or matrix)in the sample are sufficiently diluted when the sample is analysed. In this way, adverse 25 effects to the analysis instrumentation or the test result can be prevented or reduced. Typically, D, = 100. Analysis software which checks the analyser results determines the extent of diluted matrix in the sample, to see whether further dilution is necessary. Also, the 30 analysis results are processed to determine the precision of the measured analyte signal. For instance, if the analyte signal is too weak, the dilution factor may need to be WO2004/017045 PCT/GB2003/003564 - 17 reduced. Moreover, the instrument may not be able to measure analyte concentration with the required accuracy if the analyte signal is too intense (in which case the sample may require further dilution by a factor D 2 ). 5 D 2 can be calculated by comparing the matrix signal from the analyser with a pre-determined maximum level used for providing adequately accurate results. As previously described, the new dilution factor D 2 is achieved by adjusting Flow 1 of the first pump 72. As a result, the 10 dilution factor can be controlled in real time as analysis results are made available from the analyser. The flow rates of the first and second pumps, 72 and 86 respectively, are controlled by a controller or PC 88. Data from the instrument analysis results are inputted to 15 the controller along link 100. The first and second pumps are controlled via links 102 and 104 respectively. The automatic sampler can be controlled along link 106 and the switch is controlled along link 108. Flow rate information or data can be passed from the pumps (or any flow meters 20 not shown) back to the controller for use by the controller. Therefore, it is possible for the controller to change the dilution factor (if necessary) having regard for the analyser results. For example, if the results show too much matrix remains in the diluted sample for accurate analysis, 25 the controller can reduce the first pump's flow rate, thereby increasing the dilution factor, as described previously. Once the sample has been analysed and the required results obtained, the system 50 can start the dilution 30 process for a new sample, as follows. The controller stops the first and second pump 72 and 86 and the switch is moved into the initial configuration (described above). Pumps 72 WO2004/017045 PCT/GB2003/003564 - 18 and 86 are re-started and the first pump 72 then starts to pump diluent into the fifth pipe 76 via switch ports A and F, and fourth pipe 70 at a slow rate substantially less than Flow 3. With the instrument pump 86 running at, or close to 5 Flow 3, a large amount of diluent is thus drawn from container 81 and the sample is diluted to a high dilution factor and pump into the analyser instrument. The analyser continues to operate without taking any readings. First pump 72 finishes pumping diluent when all the sample in the fifth 10 pipe 76 is displaced from therein. This can be controlled by pumping the second fluid or diluent 73 at a predetermined flow rate F, for a predetermined time T, where, T > V/F 15 and V is the volume occupied by the fluid in the switch (between ports A and F) and the fifth pipe 76. This helps to ensure all the sample remaining in the fifth pipe is flushed out and does not contaminate the next sample for analysis. T 20 can be minimised by reducing the length (and hence volume) of the fifth pipe between the switch and the mixing region. At the same time, a new sample is drawn into the system by the automatic sampler 54, the first and second pipes (56 and 64) having been flushed of any sample as previously 25 described. During the second or sample pump phase (the valve 58 having been switched to the second position), the first pump 72 operates at substantially Flow 3 for an initial period and until all the diluent 73 in fifth pipe 76 is displaced 30 by sample fluid from the second pipe 64. When the fifth pipe is completely full of sample, the first pump's flow rate is reduced to Flow 1 and so dilution of the sample takes place, WO2004/017045 PCT/GB2003/003564 - 19 as described above. The time needed to completely fill the fifth pipe with sample can be calculated using the appropriate equation. In this way, the sample is pumped to the instrument at 5 an accurate flow rate required for accurate dilution and without the sample contaminating or corroding the first pump's 72 components. Furthermore, contamination of the system components is greatly reduced with the flush cycle employed in the present invention. 10 An alternative method of determining the dilution factor can include "spiking" or "lacing" the sample solution with a known substance at a known concentration level. The spike is often referred to as an Internal Standard. Analysis of the analyser's results shows how much the sample 15 has been diluted by the reduction of the level of known substance in the results. Of course, the known substances should be one which is not present in the sample or diluent before the spike is added. Such known substances might include Rhodium or Indium, for example. 20 To obtain very accurate dilution factor levels it is preferable to spike both the sample and the diluent. For example, the sample can be spiked with 100 parts per billion (ppb) concentration levels of Rhodium and 10 ppb of Indium. The diluent is not spiked with Rhodium, but is spiked with 25 indium at a concentration level of 10ppb. If the sample is diluted by, say, a factor of fifty, the Rhodium concentration is 2ppb (after dilution). The Indium internal standard is still at a concentration level of 10 ppb as both the sample and diluent contain 10 ppb of indium. 30 However, the value of Rhodium concentration varies if there is an instability in the dilution (such instability might be caused by an air bubble in the mixer, or by WO2004/017045 PCT/GB2003/003564 - 20 inconsistent mixing of sample with the diluent, for example). In the case of an air bubble passing through the system, the Rhodium concentration levels might read 1.2 ppb, followed by 1.99 ppb on the next batch and 2.0 ppb on the 5 last batch. This leads to a mean value of 1.73 ppb, or a 13.5% error of the expected dilution factor of 50:1. A correction for each batch can be made by scaling the values for each batch; the scaling factor for the first batch would be 2/1.2, the scaling factor for the second batch would be 10 2/1.99 and the scaling factor for the third batch would be 2/2.0. This can eliminate any errors in perceived concentration levels of the sample, which would otherwise be in error had the anomaly in the dilation factor not been noticed. This spiking, or use of an internal standard, 15 allows for dilutions for in excess of 50:1 without the risk of micro-bubbles or mixing effects causing errors in data. Furthermore, spiking the diluent and sample with Indium having the same levels of concentration is advantageous, particularly in a situation where the sample is pumped to 20 the mixer and fluid in the mixer is pumped to the instrument, but diluent is not actively pumped to the mixer (i.e., there is no pump on the line between the diluent vessel and the mixer, so the flow of diluent is related to the relative flows of the sample pump and instrument pump). 25 Problems can arise when a zero dilution factor is required. To achieve zero dilution, both the instrument and sample pumps should run with the same flow rates. However, if the sample pump is running slightly faster than instrument pump, then a portion of the sample is forced into the diluent, 30 contaminating the diluent. It is therefore preferable to run the sample pump with a flow rate of the order of 10% less than the instrument pump's flow rate. This way the WO2004/017045 PCT/GB2003/003564 - 21 sample is only slightly diluted. Detecting the concentration levels of Rhodium can account for, or determine this small dilution factor. The indium spike can also be used to detect and/or 5 determine any variations which might occur in the sample ionisation process. In the case of ICP-MS the ionisation occurs in a plasma torch, and variations in the torch's consistency or plasma condition can be detected by the levels of indium detected in the mass spectrum. This is so 10 because indium concentration levels should always be o10ppb, but if less than this concentration is detected then a correction can be made to factor into the result inconsistencies in ion formation, for instance. The throughput of an instrument embodying the present 15 invention can be greatly improved and less intervention from a human operator is required. Furthermore, if the dilution factor is maintained at a relatively high level, the inlet of the analyser can be prevented from becoming contaminated with matrix materials, thus reducing the downtime necessary 20 for cleaning the instrument. The pump system described above are in a 'closed' configuration, by which we mean the sample and diluent are contained in the system from the switch to the output. By keeping the system closed the equations above are maintained 25 during operation. It is therefore important to make sure the diluent and the sample do not run out during operation to prevent air entering the system. The tubing or pipe components of the pump system 50 should be made of suitably rigid materials to prevent 30 expansion or contraction under any pressure. Such expansion or contraction is undesirable since it affects the volume occupied by the sample, diluent and diluted sample. The WO2004/017045 PCT/GB2003/003564 - 22 expansion and contraction can be tolerated if their extent is determinable or predictable. The mixer should preferably be designed to ensure full mixing of the sample and diluent by creating a turbulent 5 flow in the mixing region of the pipe. The first and second pumps should provide a substantially continuous flow, without any pulsing. The flow rate from each pump can be determined by using independent flow meters disposed fore or aft of the 10 respective pump, with an appropriate feedback loop to the pump controller. Alternatively, the dilution factor can be measured by the use of an internal standard. An appropriate software programme can be used by the controller to automate the dilution of the samples and change-over from one sample 15 to the next, as described above. The controller might comprise a desktop PC with appropriate input and output devices to monitor and control the pumps and flow switching device 58, using an appropriate software programme. Examples of samples used by embodiments of the present 20 invention include drinking water, waste water, sea water, diluted acids, urine, blood, spinal fluid, dissolved solid or gaseous samples, or the like. These examples are by no means exclusive, and any liquid sample which requires analysis can be diluted prior to entering the analyser by 25 pumps which embody the present invention. Of course, an appropriate diluent is required for different samples and the choice of diluent for a given sample does not form part of the present invention. The diluent may be de-ionised water, ethanol or the like, but whatever is most suitable 30 depending on the sample being analysed. The embodiments described above provide a apparatus and method for pumping a sample into a store or buffer, WO2004/017045 PCT/GB2003/003564 - 23 relatively quickly and using an inaccurate, non-uniform flow rate pump (which is generally inexpensive). The sample is then removed or dispensed from the store using an accurate pump, at relatively slow volumeric flow rates (if required) 5 and such that the sample does not enter the accurate pump or contaminate the pump's components. In this way, cross contamination of samples or pump corrosion can be avoided. Further embodiments of the present invention will be envisaged by the skilled person, without leaving the scope 10 of the claims. For example, the embodiments have been described using in-line pumps, but it may be desirable to use other pumping systems. Also, diluent 80 and 73 can be contained in the same container. Furthermore, the wash solution in container 62 may also comprise diluent in a 15 common container with 80 and 73.
Claims (43)
1. Pump apparatus for pumping a sample to an analyser 5 for analysis, comprising; a first pump arranged to pump the sample into a buffer region at a first flow rate, and a second pump arranged subsequently to pump a second fluid into said buffer region at a second flow rate to cause 10 at least a portion of the sample to be displaced from the buffer region to the analyser, said second pump being operable so that the second flow rate is more accurately controllable than the first flow rate. 15
2. Apparatus according to claim 1, further comprising a mixer disposed downstream of the buffer region and upstream of the analyser on a buffer outlet conduit, said mixer being arranged to mix the sample with a diluent to dilute the sample before analysis. 20
3. Apparatus according to claim 1 or 2, further comprising a third pump arranged to pump the diluted sample to the analyser at a third flow rate. 25
4. Apparatus according to claim 3, wherein the diluent is pumped into the mixer at a fourth flow rate, said fourth flow rate being substantially the difference between the third and second flow rates. 30
5. Apparatus according to claim 4, wherein the third pump is arranged to pump the diluent into the mixer. WO2004/017045 PCT/GB2003/003564 - 25
6. Apparatus according to any preceding claim, wherein the buffer region is arranged to have a first and second port.
7. Apparatus according to claim 6, wherein the first pump 5 is arranged to dispose the sample into the buffer region via the first port and the second pump is arranged to disposed the second fluid into the buffer region via the second port.
8. Apparatus according to claim 6 or 7, further comprising 10 a flow switching means moveable between a first and second position, the flow switching means being so arranged that; (a) when the switching means is in the first position, the buffer region is in fluid communication with the first pump, 15 and (b) when the switching means is in the second position, the first buffer region port is in fluid communication with the mixer, and a second buffer region port is in fluid communication with the second pump. 20
9. Apparatus according to claim 8, further comprises a waste conduit so arranged that, when the switching means is in the first position, the buffer region is also in fluid communication with the waste 25 conduit.
10. Apparatus according to claim 8, wherein the switching means is arranged so that, when the switching means is in the second position, the 30 waste conduit is in fluid communication with the first pump, the first pump being arranged to pump a flush agent. WO2004/017045 PCT/GB2003/003564 - 26
11. Apparatus according to claim 8, 9 or 10, further comprising, when the switching means is in the first position, the second pump is in fluid communication with the outlet 5 conduit disposed between the mixer and buffer region, so that the second fluid can be pumped into the outlet conduit for displacement of the sample fluid or second fluid therein. 10
12. Apparatus according to claim 2 or 11, wherein the mixing region comprises two or more input tubes, a mixing portion and an exit tube, a first input tube being arranged for communicating the sample fluid to the mixing portion from the buffer region, 15 and a second input tube being arranged for communicating the diluting agent to the mixing portion.
13. Apparatus according to claim 11 or 12, further 20 comprising, when the switching means is in the second position, the second pump is arranged to pump the sample fluid through the mixing region at the second flow rate, and the third pump is arranged to pump the diluted sample 25 fluid at a third flow rate
14. Apparatus according to any preceding claim, further comprising a controller for monitoring and/or adjusting at least one of the first, second or third pump means, and/or 30 the switching means, during operation. WO2004/017045 PCT/GB2003/003564 - 27
15. Apparatus according to claim 14, wherein the controller is a PC.
16. Apparatus according to claim 14 or 15, wherein the 5 controller is arranged to receive analysis data from the analyser.
17. Apparatus according to claims 13 and 16, wherein the third rate is substantially equal to, or greater than, the 10 second rate, and wherein the controller is arranged to adjust the first and/or third rate in response to received analysis data.
18. Apparatus according to claim 17, wherein the controller 15 is arranged to adjust the flow rates in real time.
19. Apparatus according to claim 1, wherein the analyser is a mass spectrometer, or an identity couple plasma mass spectrometer. 20
20. Apparatus according to claim 1, wherein the second pump means comprise a piston pump.
21. An analyser for analysing a sample fluid, comprising a 25 pumping system according to any preceding claim.
22. An analyser according to claim 21, wherein the analyser is a mass spectrometer, or an inductively couple plasma mass spectrometer. 30
23. A method for pumping a sample fluid for analysis to an analysis instrument using a pumping apparatus comprising, WO2004/017045 PCT/GB2003/003564 - 28 a buffer region for temporarily storing the sample fluid, the buffer region being arranged with at least two ports, disposing the sample fluid in the buffer region using a 5 first pump means at a first flow rate through a first port, and the method comprising, pumping a second fluid into the at least partially filled buffer region at a second flow rate through a second 10 port, using a second pump means, thereby displacing the sample fluid therein to the analyser. Whereby the second pump means is more accurately controllable than the first pump means 15
24. A method according to claim 23, wherein the apparatus further comprises a flow switching means moveable between a first and second position, the flow switching means being so arranged that; 20 (a) when the switching means is in the first position, the buffer region is in fluid communication with the first pump, and (b) when the switching means is in the second position, the first buffer region port is in fluid communication with the 25 mixer, and a second buffer region port is in fluid communication with the second pump. the method further comprising, pumping the sample into the buffer when the flow switching means is in the first position using the first 30 pump, switching the flow switching means to the second position, and WO2004/017045 PCT/GB2003/003564 - 29 pumping the second fluid into the buffer region using the second pump for displacement of the sample therein.
25. A method according to claim 24, the apparatus further 5 comprising a waste conduit so arranged that, when the switching means is in the first position, a buffer region port is in fluid communication waste conduit, the method further comprising, pumping excess fluid in the buffer region to the waste 10 conduit.
26. A method according to claim 25, further comprising, when the switching means is in the second position, the waste conduit is in fluid communication with the first pump, 15 and the first pump pumps a flush agent.
27. A method according to any of claims 24 to 26, further comprising, when the switching means is in the first position, the 20 second pump is in fluid communication with the outlet conduit, and the second pump pumps the second fluid into the outlet conduit for displacement of the sample fluid or second fluid therein. 25
28. A method according to any of claims 24 to 27, the apparatus further comprising, a mixing region for mixing the sample fluid with a diluting agent, and 30 a third pump means pumps diluted sample fluid from the mixing region to the analyser, WO2004/017045 PCT/GB2003/003564 - 30 wherein, the mixing region is disposed between the outlet conduit and the analyser; the method further comprising, when the switching means is in the second position, 5 the second pump means pumps sample fluid into the buffer region at a second flow rate, the third pump means pumps the diluted sample fluid at a third flow rate, and the third pump means pumps the diluting agent at a 10 fourth flow rate substantially equal to the difference of the third and second flow rate.
29. A method according to any of claims 24 to 28, wherein the apparatus further comprises a controller which monitors 15 and/or adjusts at least one of the first, second or third pump means, and/or the switching means.
30. A method according to claim 29, wherein the controller receives analysis data from the analyser. 20
31. A method according to claim 28 and 30, wherein the third rate is substantially equal to, or greater than, the second rate, and wherein the controller adjusts the first and/or third 25 rate in response to the received analysis data.
32. A method according to claim 31, wherein the controller adjusts the flow rates in real time. 30
33. A method for diluting a sample fluid, using apparatus according to any of claims 1 to 22, and a method according to any of claims 23 to 32. WO2004/017045 PCT/GB2003/003564 - 31
34. A computer program which, when run on a computer, carries out the method according to any of claims 23 to 33. 5
35. An electronic carrier means on which is stored the computer program according to claim 33.
36. A method of preventing contamination of a first pump means with a sample, the method comprising; 10 disposing the sample in an intermediary region using a second pump, displacing the sample from the intermediary region by pumping a second fluid into said intermediary region using the first pump means. 15
37. A diluting system for diluting a sample fluid for analysis, comprising; a buffer region for storing the sample fluid arranged with an input and output, 20 a first pump means for pumping the sample fluid into a sample fluid buffer region through the input, a second pump means for pumping a second fluid into the buffer region through the output, an outlet conduit arranged for flow of the sample fluid 25 and/or fluid to the analyser a mixing region for mixing the sample fluid with a diluting agent, a third pump means for pumping diluted sample fluid from the mixing region to the analyser, and 30 a flow switching means moveable between a first and second position, so arranged that, WO2004/017045 PCT/GB2003/003564 - 32 when the switching means is in the first position, the buffer region input is in communication with the first pump and the sample fluid can be pumped into the buffer region, and 5 when the switching means is in the second position, the buffer region input is in communication with the outlet conduit, and the buffer region output is in communication with the second pump so that the second fluid can be pumped into the buffer region for displacement of the sample fluid 10 therein, and wherein, the mixing region is disposed between the outlet conduit and the analyser.
38. A method for diluting a sample fluid for analysis using a dilution system comprising, 15 a buffer region for storing the sample fluid arranged with an input and output, an outlet conduit arranged for flow of the sample fluid and/or the second fluid to the analyser, a mixing region for mixing the sample fluid with a 20 diluting agent, and a third pump means arranged to pump diluted sample fluid from the mixing region to the analyser, the mixing region is disposed between the outlet conduit and the analyser, and 25 a flow switching means moveable between a first and second position, so arranged that, when the switching means is in the first position, the buffer region input is in communication with a first pump, and when the switching means is in the second position, the buffer region input is 30 in communication with the outlet conduit, and the buffer region output is in communication with a second pump; the method comprising, WO2004/017045 PCT/GB2003/003564 - 33 pumping the sample fluid into the sample fluid buffer region through the input when the switching means is in the first position, using the first pump means, switching the switching means to the second position, 5 pumping a fluid into the buffer region through the output, thereby displacing the sample fluid therein to the outlet conduit, when the switching means is in the second position, the second pump means pumps the second fluid into the buffer 10 region at a first flow rate, such that the sample fluid proceeds through the mixing region at the first flow rate, the third pump means pumps the diluted sample fluid at a third flow rate, and the third pump means pumps the diluting agent at a 15 second flow rate substantially equal to the difference of the third and first flow rate.
39. A method of pumping a fluid sample through a dilutor using a first pump, for analysis of the diluted fluid sample 20 downstream of said dilutor, said first pump being isolated from said fluid sample, the method comprising: disposing said fluid sample in an intermediary region using a second pump, said intermediary region having a first and second port through which fluid can flow, 25 displacing at least a portion of said fluid sample from the intermediary region through the first port by inserting a second fluid into the intermediary region through the second port using the first pump, the first port being in fluid communication with the diluter so that the at least a 30 portion of said fluid sample is displaced into the diluter from the intermediary region. WO2004/017045 PCT/GB2003/003564 - 34
40. A method according to any of claims 23 to 39, further comprising; disposing an internal standard into the sample, said internal standard comprising a known concentration of a 5 predetermined substance, and determining the factor by which the sample is diluted by comparing the detected concentration of the internal standard with the known concentration of the internal standard in the undiluted sample. 10
41. A method according to claim 40, wherein a second internal standard comprising a known concentration of a second predetermined substance is disposed in the sample and the diluent at the same second concentration levels. 15
42. A method according to claim 40 or 41, further comprising; determining the dilution factor from the amount of the first internal standard detected by the analyser, 20 determining a correction factor by comparing the determined dilution factor with an expected dilution factor, and using the correction factor to correct analyser data. 25
43. Apparatus according to claim 1, wherein the sample and/or the diluent contain an internal standard which comprises a predetermined amount of a known substance, and a dilution factor by which the sample is diluted is calculable by comparing the detected amount of said internal 30 standard by the analyser with the amount of internal standard in the sample or diluent.
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| PCT/GB2003/003564 WO2004017045A1 (en) | 2002-08-14 | 2003-08-14 | Method and apparatus for pumping and diluting a sample |
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| US5414259A (en) * | 1994-01-05 | 1995-05-09 | Duquesne University Of The Holy Ghost | Method of speciated isotope dilution mass spectrometry |
| GB2285837B (en) * | 1994-01-24 | 1998-05-13 | Varian Australia | Peristaltic pump |
| AU681765B2 (en) * | 1994-04-28 | 1997-09-04 | Mitsubishi Materials Corporation | Continuous flow analyzing method and apparatus |
| JP3572792B2 (en) * | 1996-04-04 | 2004-10-06 | 東ソー株式会社 | Pretreatment device |
| US5988987A (en) * | 1996-08-28 | 1999-11-23 | Fia Solutions, Inc. | Method for merging and/or ratio blending aliquant |
| US6211956B1 (en) * | 1998-10-15 | 2001-04-03 | Particle Sizing Systems, Inc. | Automatic dilution system for high-resolution particle size analysis |
| US6324924B1 (en) * | 1999-04-06 | 2001-12-04 | Roger Peterson | Sampling system including a sample additive mixing feature |
| JP2000292318A (en) * | 1999-04-07 | 2000-10-20 | Yokogawa Analytical Systems Inc | High-speed collecting method of sample and high-speed diluting device using it |
| JP3476417B2 (en) * | 2000-06-05 | 2003-12-10 | 株式会社島津製作所 | Analytical method by liquid chromatography |
-
2002
- 2002-08-14 GB GBGB0218949.6A patent/GB0218949D0/en not_active Ceased
-
2003
- 2003-08-14 JP JP2004528674A patent/JP2005535893A/en active Pending
- 2003-08-14 WO PCT/GB2003/003564 patent/WO2004017045A1/en active Application Filing
- 2003-08-14 EP EP03787896A patent/EP1540305A1/en not_active Withdrawn
- 2003-08-14 AU AU2003255792A patent/AU2003255792A1/en not_active Abandoned
- 2003-08-14 CA CA002497648A patent/CA2497648A1/en not_active Abandoned
- 2003-08-14 US US10/524,706 patent/US20060104827A1/en not_active Abandoned
- 2003-08-14 CN CN03819412.0A patent/CN1675530A/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| CA2497648A1 (en) | 2004-02-26 |
| GB0218949D0 (en) | 2002-09-25 |
| US20060104827A1 (en) | 2006-05-18 |
| CN1675530A (en) | 2005-09-28 |
| JP2005535893A (en) | 2005-11-24 |
| WO2004017045A1 (en) | 2004-02-26 |
| EP1540305A1 (en) | 2005-06-15 |
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Free format text: AN APPLICATION TO EXTEND THE TIME FROM 14 MAR 2005 TO 14 OCT 2005 IN WHICH TO ENTER THE NATIONAL PHASE HAS BEEN FILED . |
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| NB | Applications allowed - extensions of time section 223(2) |
Free format text: THE TIME IN WHICH TO ENTER THE NATIONAL PHASE HAS BEEN EXTENDED TO 14 OCT 2005. |
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| PC1 | Assignment before grant (sect. 113) |
Owner name: THERMO FISHER SCIENTIFIC, INC Free format text: FORMER APPLICANT(S): THERMO ELECTRON CORPORATION |
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| MK4 | Application lapsed section 142(2)(d) - no continuation fee paid for the application |