The present invention relates to the field of settlement analysis such as may be employed to characterise samples from a process or flow. More specifically, the present invention concerns improvements to settlement analysers that provides improved determination of levels, quantities and/or interface layer depth of samples. Such samples may be retrieved by sampling apparatus in the process or flow. The present invention may be implemented in standalone apparatus that receive and analyse samples in containers.
In many processes, it is required to analyse a sample (e.g. liquid or other fluid) from within the process while maintaining a stable and controlled environment. Additionally, such processes may involve liquids with suspended solids, which are also required to be analysed, placing additional burden on a sampling system. Since the analysis should be performed on a sample taken from within the process the sampling system and the analysis itself must be reliable and robust to provide extended periods of service without any intervention by the operator or remedial action.
Such reliability and robustness is provided, for example, by the Applicant's proprietary sampling apparatus, for example as described in UK Patent Number GB2549197. However, there remains a need for a reliable and robust approach to the analysis of samples such as may be obtained using such sampling apparatus.
For example, one of the most common tests carried out in activated sludge wastewater treatment is the sludge settlement test in which a sample of mixed liquor is collected in a sample container (for example a sample tube or cylinder) and allowed to settle for 30 minutes. A visual measurement is then taken of the amount of settled solids at the bottom of the sample tube or cylinder using gradations provided on the sample tube or cylinder itself. However this information is not entirely useful without knowledge of other parameters or characteristics of the sludge, which must be determined by other separate processes or analyses.
In the water industry, mixed liquor suspended solids (MLSS) meters and turbidity meters are used to provide some of the data required, but these increase the amount of equipment required in order to make meaningful and accurate measurements.
In the oil and gas industry, volume displacement vessels housed in sight glasses that are mechanically linked to control actuators (or trolls) are utilised in separation tanks or very expensive and complex gamma ray detection systems are employed.
In multiphase flows in the oil and gas industry, it is desirable to know the amounts and relative proportions of crude oil, natural gas and water in a particular flow. Conventional multiphase flow meters (MPFMs) are very complex and expensive apparatuses and require knowledge of composition or at least phase fraction to operate effectively. This composition data is typically taken from assumed values or samples (which are taken infrequently). There are therefore several disadvantages of conventional MPFMs.
It is an object of at least one aspect of the present invention to obviate and/or mitigate one or more disadvantages of known/prior apparatus such as described above.
Furthermore, it is an object of at least one embodiment of the present invention to provide an apparatus that provides one or more of the above-mentioned desired features and/or advantages.
Further aims and objects of the invention will become apparent from reading the following description.
According to a first aspect of the invention, there is provided a settlement analyser comprising an array of emitters and at least one array of detectors, a sample volume between the array of emitters and the at least one array of detectors, wherein the settlement analyser is configured to analyse a sample within the sample volume by sequentially emitting light from the array of emitters, and detecting light which arrives at the at least one array of detectors via the sample volume.
Preferably, the at least one array of detectors comprises an array of detectors which is diametrically (or directly) opposite the array of emitters with respect to the sample volume. Put another way, an array of detectors may be positioned to primarily detect light transmitted through the sample volume.
Preferably, the settlement analyser is configured to determine an optical profile of the sample within the sample volume by detecting light emitted by each emitter of the array of emitters at a corresponding detector of the first array of detectors. The optical profile may correspond to a transmittance profile, a clarity profile, a turbidity profile, or the like. Optionally, the settlement analyser is configured to determine the optical profile as a function of time by repeating the sequence.
Optionally, the at least one array of detectors comprises an array of detectors which is oriented (or directed) at 90 degrees to the array of emitters (or the direction of light emitted by the emitters) with respect to the sample volume. Put another way, an array of detectors may be positioned to primarily detect light scattered from within the sample volume. Note that such an array of detectors need not be oriented (or directed) at 90 degrees to achieve this aim and as such the term “90 degrees” shall be understood to include any position which is not diametrically (or directly) opposite the array of detectors.
In an embodiment of the invention, the settlement analyser comprises a first array of detectors which is diametrically (or directly) opposite the array of emitters with respect to the sample volume, and a second array of detectors which is oriented (or directed) at 90 degrees to the array of emitters (or the direction of light emitted by the emitters) with respect to the sample volume.
Optionally, the settlement analyser is configured to determine an optical profile of the sample within the sample volume by detecting light emitted from each emitter of the array of emitters and scattered within the sample volume at a corresponding detector of the second array of detectors. The optical profile may correspond to a turbidity profile, a fluorescence profile, or the like. Optionally, the settlement analyser is configured to determine the optical profile as a function of time by repeating the sequence.
Preferably, the settlement analyser is configured to determine the location of one or more interfaces within the sample based on the optical profile of the sample.
Preferably, the number of detectors in each of the at least one array of detectors is equal to the number of emitters in the array of emitters.
Preferably, the array of emitters is oriented vertically. Preferably, the array of emitters is a linear array. Alternatively, the array of emitters is interleaved or staggered.
Preferably, at least one array of detectors is oriented vertically. Preferably, at least one array of detectors is a linear array. Alternatively, or additionally, at least one array of detectors is interleaved or staggered.
Preferably, the emitters comprise infrared light emitting diodes and the detectors comprise infrared sensitive photodiodes.
Preferably, the settlement analyser comprises an integrated controller or processor. Alternatively, the settlement analyser comprises a separate controller or is connectable to a separate controller.
Preferably, light is emitted from the array of emitters in a linear sequence. Alternatively, light is emitted from the array of emitters in a non-linear sequence. Optionally, the sequence is selected to minimise cross-talk.
Optionally, the sample volume is configured, arranged, adapted or otherwise able to receive the sample within a sample holder.
Optionally, the settlement analyser further comprises a visual display to display one or more results of the analysis. Preferably, the visual display comprises an LCD screen, AMOLED screen, or the like.
According to a second aspect of the invention, there is provided a method of analysing settlement within a sample comprising;
providing an array of emitters and at least one array of detectors;
locating the sample between the array of emitters and the array of detectors;
sequentially emitting light from the array of emitters; and
detecting light which arrives at the array of detectors via the sample.
Preferably, the method comprises determining a first optical profile of the sample by detecting light emitted by each emitter of the array of emitters and passing through the sample at a corresponding detector of a first array of detectors. The first optical profile may correspond to a transmittance profile, a clarity profile, a turbidity profile, or the like. Optionally, the method comprises determining the first optical profile as a function of time by repeating the sequence.
Optionally, the settlement analyser is configured to determine a second optical profile of the sample by detecting light emitted from each emitter of the array of emitters and scattered within the sample volume at a corresponding detector of a second array of detectors. The second optical profile may correspond to a turbidity profile, a fluorescence profile, or the like. Optionally, the method comprises determining the second optical profile as a function of time by repeating the sequence.
Preferably, the method comprises determining the location of one or more interfaces within the sample based on the first and/or second optical profiles of the sample. Preferably, determining the location of the one or more interfaces comprises identifying discontinuities in the first and/or second profile. A discontinuity might, for example, be a difference in the amount of light received at (and hence a voltage or other output from) two or more detectors located in the vicinity of an interface.
Optionally, the method further comprises detecting light emitted by at least one emitter of the array of emitters at one or more detectors adjacent to the corresponding detector of the first and/or second array of detectors. This will increase the resolution of the first and/or second optical profile and of the location of any interfaces in this region.
Preferably, this is responsive to a determination that there is an interface within the sample in the region of said at least one emitter and its corresponding detector.
Alternatively, the method comprises detecting light emitted by each emitter of the array of emitters at each detector of the first and/or second array of detectors.
Optionally, the method comprises determining MLSS concentration within the sample based on a ratio between the second profile (which relates to scattered light) and the first profile (which relates to transmitted light) when the sample is well-mixed (for example at the start of the analysis when the sample has just been obtained or just inserted into the sample volume).
Optionally, the method comprises determining an SV30 number for the sample based on the location of an interface within the sample. Optionally, the method comprises determining an SVI value based on the MLSS concentration and the SV30 number.
Preferably, the method comprises emitting light from the array of emitters in a linear sequence. Alternatively, light is emitted from the array of emitters in a non-linear sequence. Optionally, the sequence is selected to minimise cross-talk.
Embodiments of the second aspect of the invention may comprise features corresponding to the preferred or optional features of the first aspect of the invention or vice versa.
According to a third aspect of the invention, there is provided an apparatus for obtaining samples from a process or flow, the apparatus comprising a sample chamber comprising at least one inlet and at least one outlet, a dam positioned in the chamber between the at least one inlet and the at least one outlet, and a gate moveable within the chamber between a first position and a second position to eject a first sample from the chamber via the at least one outlet and simultaneously draw a second sample into the chamber via the at least one inlet;
wherein the apparatus further comprises at least one settlement analyser according to the first aspect (within the sample chamber).
A settlement analyser may be located on one or both sample-facing surfaces of the dam or the gate.
Advantageously, the dam prevents fluid communication between the at least one inlet and the at least one outlet.
Preferably, the at least one inlet is located proximal a first side of the dam and the at least one outlet is located proximal a second, opposite side of the dam.
Preferably, the sample chamber comprises a housing arranged, adapted or otherwise configured for location in the process or flow.
Preferably, the at least one inlet comprises a first opening on an outer surface of the housing and a second opening on an inner surface of the housing such that a sample is drawn into the sample chamber directly from the process or flow.
Preferably, the at least one outlet comprises a first opening on an outer surface of the housing and a second opening on an inner surface of the housing such that a sample is ejected from the sample chamber directly into the process or flow.
Preferably, the first position of the gate is proximal a first side of the dam and the second position of the gate is proximal a second, opposite side of the dam. Optionally, the gate is configured to abut the dam in the first and/or second position. A first face of the gate, corresponding to the first side of the dam, may be shaped to match the first side of the dam.
Preferably, the gate is configured to pivot about a longitudinal axis through the chamber.
Preferably, the apparatus further comprises at least one sensor to enable a measurement to be performed within the sample chamber.
Optionally, at least one sensor is located on the gate. At least one sensor may be located on one or both faces of the gate.
Alternatively, or additionally, at least one sensor is located on the dam.
The at least one sensor may be selected from the group comprising oxygen sensors, temperature sensors, chemical sensors, pH sensors, turbidity sensors, density sensors, conductivity sensors, salinity sensors and contact sensors.
Optionally, the apparatus further comprises means to agitate a sample within the sample chamber.
Optionally, the means to agitate a sample comprises one or more pumps. The one or more pumps may be located on or in the dam, and may be micro-pumps, or one or more outlets may be provided on the dam in fluid communication with one or more pumps or micro-pumps.
Optionally, the apparatus further comprises means to inoculate a sample within the sample chamber. The means may comprise one or more outlets on the dam in fluid communication with an external source of inoculant. Preferably, outlets are provided on both faces of the dam.
Preferably, the gate is moveable between the second position and the first position to eject a sample from the chamber via the at least one inlet (which becomes an outlet) and simultaneously draws another sample into the chamber via the at least one outlet (which becomes an inlet).
Preferably, reciprocation of the gate between the first position and the second position causes a plurality of samples to be drawn into the chamber and subsequently ejected.
Preferably, the apparatus comprises a plurality of inlets and a plurality of outlets. Preferably, the plurality of inlets and outlets are distributed vertically in the sample chamber. They may be distributed evenly between the top and the bottom of the sample chamber.
Preferably, the gate comprises one or more wipers to assist in drawing samples into the sample chamber and/or ejecting samples from the sample chamber. The wiper may provide a seal between the gate and the inner surface of the sample chamber.
Preferably, the sample chamber is substantially cylindrical. Preferably, a lower portion of the sample chamber is substantially frusto-conical.
The gate may be hollow. The dam may be hollow. The internal volumes of the gate and/or the dam may house one or more sensors, micro-pumps and/or conduits for the delivery of inoculant to the sample chamber.
The apparatus may comprise a motor to move the gate. The motor may be operatively connected to the dam via one or more gears. The motor may be housed within a top chamber of the apparatus. The top chamber may further house a controller.
Optionally, the apparatus is, at least in part, hermetically sealed. Preferably, the top chamber of the apparatus is hermetically sealed. Alternatively, one or more components within the top chamber of the apparatus are hermetically sealed.
Preferably, the apparatus comprises communications means. The communications means may comprise one or more conduits for connection to a controller. Alternatively, the communications means may be wireless, and may comprise Wi-Fi, Bluetooth, NFC or the like.
The apparatus may comprise a mounting post. The mounting post may be of a predetermined length corresponding to a desired depth to which the apparatus is to be inserted in the process or flow. The mounting post may be hollow so as to accommodate one or more conduits.
Embodiments of the third aspect of the invention may comprise features corresponding to the preferred or optional features of the first or second aspects of the invention or vice versa.
According to a fourth aspect of the invention there is provided a method of analysing a sample from a process or flow, comprising obtaining a sample from a process or flow using a sampling apparatus (such as the apparatus of the third aspect) and analysing the sample in accordance with the second aspect.
Preferably, obtaining a sample from the process or flow comprises providing an apparatus according to the third aspect within the process or flow, and moving the gate between the first position and the second position or vice versa.
Optionally, the method comprises agitating the one or more samples within the sample chamber.
Optionally, the method comprises inoculating the one or more samples within the sample chamber.
Optionally, the method comprises altering the process or flow responsive to the analysis.
Embodiments of the fourth aspect of the invention may comprise features corresponding to the preferred or optional features of the first, second or third aspects of the invention or vice versa.
According to further aspects of the invention, there is provided a settlement analyser and a method of analysing settlement of a sample substantially as herein described with reference to the appended drawings.
There will now be described, by way of example only, embodiments of aspects of the invention with reference to the drawings (like reference numerals being used to denote like features), of which:
Embodiments of the present invention are illustrated in and will now be described with reference to
Between the emitter array 53 and the detector array 55 is defined a sampling channel 59. Fluid can enter or be placed in the sampling channel 59 in any way, but by way of example the settlement analyser may be located on or in the wall of a vessel (or part of a vessel) into which fluid is received and thereby exposed to the fluid directly, or the fluid can be inserted in the sampling channel within a suitable container such as a test tube or sample bottle. Exemplary embodiments corresponding to these arrangements are described further below and with reference to
In this embodiment, the emitters 54 are infrared LEDs, and the detectors 56 are infrared sensitive photodiodes. Infrared is preferred because of the cheap availability of components, low divergence of infrared LEDs, and the relatively low level of interference or disturbance from other sources of light in the environment. Furthermore, small component size allows for ease of mounting (e.g. on PCBs) as well as enabling close spacing of adjacent emitters/detectors. Of course, any suitable emitter/detector arrangement can be employed without departing from the scope of the invention.
The settlement analyser 51 operates by illuminating one of the emitters 54 and detecting light received from the emitter 54 at the corresponding detector 56. The emitter 54 is then switched off and a subsequent emitter 54 is illuminated and light from that emitter 54 is detected at its corresponding detector 56. By repeating this for all of the emitter-detector pairs an instantaneous transmissivity (or transmittance) profile for the sample contained within the sampling channel is obtained. If the sample is well mixed it is to be expected that the profile will be relatively consistent whereas if the sample is settled it is to be expected that the profile may vary and correspond to any layers which may form. It will be understood that the amount of light received by a photodetector 56 will be proportional to the transmittance of the sample (affected by absorption, reflection and scattering within the sample) in the region between that photodetector and the corresponding emitter 54.
In ways that will be well known to the skilled person, or readily implemented, repeated measurements can be taken to determine a mean. This mean may be monitored as a function of time.
The sequence in which each emitter 54 emits light is preferably in order, for example from top to bottom or bottom to top, although the emitters 54 can emit light in any order. In the ten emitter/detector arrays shown in
In some cases it may be practical to illuminate multiple emitters at the same time, for example in a sequence such as 1&6-2&7-3&8-4&9-5&10. It is however foreseen that in some cases this might lead to undesirable cross-talk. That said, if the angle of illumination of a particular emitter is known, or can be controlled for example by shielding, it will be possible to avoid cross-talk by ensuring that the illumination from emitters illuminated at the same time do not overlap or at least that the illumination from emitters illuminated at the same time does not impinge on detectors corresponding to other illuminated emitters. Testing in a particular implementation would readily reveal whether cross-talk was likely to occur and the sequence could be adjusted accordingly. For example, in the case of emitters having a relatively narrow angle of illumination and many emitters and detectors, it is foreseen that several emitters might be illuminated at the same time.
In many cases it will be sufficient to detect the light emitted by a particular emitter 54 by a corresponding detector 56 opposing the emitter 54, and this might be particularly true if this results in an acceptable resolution. As discussed below however it will be possible and in some cases desirable and/or advantageous to detect the light emitted by a particular emitter at more than one detector 56. It is also noted above that emitters and detectors need not be provided in pairs and an example of how this might be implemented in practice is also discussed further below.
Note that it is envisaged that the settlement analyser may be provided with an integrated controller or processor which is programmed or otherwise configured to control the emitters and receive and process signals or outputs from the detectors, and perform analysis thereof. Otherwise, the settlement analyser can be connected to a separate controller or processor, for example a PC or dedicated microcontroller (such as a suitably programmed Arduino or Android device), for example via USB, Bluetooth, NFC or WiFi, for this purpose.
An important measurement that the detectors 158 can be used to make is a measurement of the mixed liquor suspended solids (MLSS) concentration. In a well mixed sample, MLSS concentration is proportional to the ratio of scattered light to transmitted light. Accordingly, if simultaneous measurements are taken with detectors 156 and 158 this can be calculated. The skilled person will realise that with an array of emitters and detectors a measurement of MLSS can be taken at each emitter-detector pair (or other combinations as envisaged and discussed below) and a mean value determined. When placing a sample in the sample volume it may be beneficial to carry out this analysis before the sample is allowed to settle, preferably when well-mixed, thus giving an MLSS value that can be employed later in the analysis process (see below).
In a very simple example of a sludge sample placed in the sample volume it will be appreciated that, over time, the sample will settle resulting in separation of the sample into sediment or settled solids towards the bottom of the sample volume and supernatant liquid or liquor above the sediment or settled solids. Knowledge of the height at which the boundary between these regions lies is an important factor in determining the total suspended solids for a particular sample, which is a key piece of information in wastewater treatment applications where it can determine whether water from which the sample has been drawn can be reused and how. Any manner of processing decisions can be made on the basis of the information obtained by the settlement analyser.
In another example, in the case of multiphase flows in the oil and gas industry it is helpful to know the amounts of crude oil, natural gas and water in a sample taken from the flow and identifying interface levels or locations allows a determination of the amounts of each constituent in the flow. The analyser can be used in production monitoring for reservoir optimisation; knowledge of what is being recovered from a particular reservoir and in what fractions can be used to control production rates and maximise (or at least increase) reservoir integrity and production. This information can also provide an input to allocation; monitoring component flow rates provides a means for producers to ensure correct fluid amounts are allocated back after commingling and subsequent separation. It will also be possible to monitor and trend parameters that influence the formation of scales, hydrates, sand and cause other flow assurance problems. It is envisaged that not only may the analyser provide improved input of composition or at least phase fraction to MPFMs, but it may provide an alternative to MPFMs for monitoring multiphase flows or supplement existing or conventional arrangements.
The resolution of the settlement analyser 51,151 is limited by the minimum separation of the emitters 54,154 and the detectors 56,156, 158. By way of example, an infrared LED or infrared photodiode may have a diameter of 5 mm. Assuming zero spacing between adjacent infrared LEDs or photodiodes, the maximum resolution that can be achieved in normal operation is 5 mm. Put another way, without practicing any of the procedures described herein to improve resolution through clever operation of the settlement analyser, this is the maximum uncertainty in any determination of the location of, for example, an interface between two different layers.
However, the resolution of the settlement analyser can be improved by interleaving or staggering additional arrays of emitters and detectors.
The resolution of the settlement analyser can alternatively (or indeed additionally) be improved in other ways. For example, a first emitter 54, 154, 354, 454 in the array 53, 153, 353, 453 can be illuminated and light detected at every one of the detectors 55, 155, 355, 455 in the array 53, 153, 353, 453 (simultaneously or sequentially). Once all of the emitters 54, 154, 354, 454 in the array 53, 153, 353, 453 have been illuminated and light detected at every one of the detectors 55, 155, 355, 455 in the array 53, 153, 353, 453 for each emitter, the data can be processed to determine with improved accuracy the location of any interfaces and/or the depth of any interface layers between the fractions in the sample volume.
In practice, it may be burdensome and indeed unnecessary to obtain and process data from every detector for each emitter. This is particularly the case when the sample being analysed is such that a meaningful or measurable amount of light emitted from any particular emitter is unlikely to reach particular detectors, or for example where there are multiple interfaces between different regions of a settled or otherwise separated sample. As such, and as intimated above, signals received by detectors from their respective emitters can be analysed in order to ascertain a relatively coarse determination of where the interface between two layers in the sample volume lies and/or the depth of any interface layers. For example, emitter-detector pair 9 may produce a relatively low voltage signal whereas emitter-detector pair 10 might produce a relatively high voltage signal. From this information it can be inferred that (following the sludge settlement example) the interface between the settled solids and the supernatant liquor lies somewhere between emitter-detector pairs 9 and 10. By detecting the light detected by detector 10 from emitter 9, and likewise the light detected by detector 9 from emitter 10, it is possible to more accurately determine the location and/or the depth of the interface between these emitter-detector pairs because detector 9 will produce a higher voltage signal and detector 10 will produce a lower voltage signal, the increase and reduction being proportional to the ratio of settled solids to supernatant liquor in this region and hence where the interface lies in this region. Obtaining measurements from other adjacent detectors, say 8 and 11, will increase the certainty of the level determination.
A combination of one or more of the possible modifications above can give rise to a significant increase in resolution of a particular settlement analyser in use. For example, in the case of a settlement analyser having ten emitter-detector pairs the resolution can be effectively doubled by detecting light received from an emitter by its respective detector and the two adjacent detectors. A small correction factor can be applied for the slight increase in absorption; again this correction factor might be determined by calibrating the analyser using a calibration sample or simply by accounting for the slightly increased absorption resulting from a slightly increased optical pathlength.
As noted above it is also not necessary to provide emitters and detectors in pairs. By way of example, in an embodiment (not shown) there may be provided an array of, say, ten emitters corresponding to the array 53 of emitters 54 shown in
At the start of the test most of the sensors provide a clarity measurement of between 0.2 and 0.3, corresponding to a relatively flat optical profile, which demonstrates that the sample is quite well mixed at this point. It can be observed that the clarity decreases in the regions of sensors 1 to 5 and increases in the regions of 12 to 24 and plateaus within a few minutes. The optical profile continues to change over time and clarity in the regions of sensors 6 to 11 take longer to plateau but it is clear that even by 10 minutes into the test period the sample has settled into distinct regions; the regions of relatively high clarity corresponding to the supernatant liquor separating out towards the top of the sample volume and the regions of relatively low clarity corresponding to the solids settling towards the bottom of the sample volume. Notably, the clarity measurement at sensor 6 does not reach plateau until near the end of the test with a few minutes remaining, after which the optical profile (which comprises two clear and distinct regions) is relatively continuous. This would tend to support that 30 minutes is sufficient to make a meaningful determination of the settlement level (at least in this case).
Monitoring the settlement level or the optical profile of the sample as a function of time has other implications and benefits; tests performed on other samples may reveal that settlement (when the optical profile becomes consistent) occurs much sooner in which case it would be reasonable to terminate the test earlier. Conversely, settlement may still be underway in which case it would be reasonable to allow the test to continue until all sensor measurements have plateaued. Such a determination could be made manually or automated.
At the end of the test period, sensors 1 to 5 give a clarity measurement of between 0 and about 0.12, and sensors 6 to 24 give a clarity measurement of between about 0.8 and 0.96. The interface between the supernatant liquor and the settled solids is clearly in the region between sensor 5 and sensor 6, as evidenced at least by the significant difference in clarity between respective sensors (or discontinuity in the optical profile). As the location of these sensors is known it is therefore possible to determine the percentage of solids in the sample volume. As the sensors are separated by 5 mm, the height of the sample volume is 130 mm, and the lowest numbered sensor which exhibits significant attenuation of light is sensor 5, the percentage of the sample volume occupied by the solids is approximately:
As intimated above, the resolution of the measurements can be increased in several ways and the precision of the level determination and measurements derived therefrom improved as a result. For example, monitoring light received from emitter 5 at sensor 6 and vice versa would enable a more accurate determination of the location of the interface (as described above).
An advantage of taking measurements throughout the settlement process, rather than simply observing a well mixed sample at the start and determining the settlement level at the end of the 30 minute test period, is that the behaviour of the sample can be analysed. For example, if the sample settles quickly it can indicate that the sludge is old, whereas if the sample settles slowly it can indicate that the sludge is young.
The duration of the test, 30 minutes, is significant because as noted in the background above one of the most common tests carried out in activated sludge wastewater treatment is the sludge settlement test in which a sample of mixed liquor is collected in a sample container (for example a sample tube or cylinder) and allowed to settle for 30 minutes, after which a measurement is taken of the amount of settled solids at the bottom of the sample tube or cylinder—visually, usually using gradations provided on the sample tube or cylinder itself. If the mixed liquor suspended solids (MLSS) concentration is known this measurement, sometimes referred to as the SV30 number, can be used to calculate the sludge volume index (SVI) which is used to describe the settling characteristic of the sample.
It will therefore be understood that the settlement analysers described herein are capable of making improved measurements of MLSS concentration (based on a ratio of scattered light to transmitted light in a well mixed sample), SV30 numbers (based on a level determination following a 30 minute settlement period) and hence SVI values (determined from the MLSS and SV30 values) without the need for manual intervention, and by monitoring the sample (for example clarity at each measurement location) as a function of time the behaviour of the sample can be analysed to determine other characteristics such as whether the sample is old or young.
Turbidity is another useful measure of the quality of a sample of water (or other fluid). Turbidity is proportional to the concentration of particles suspended in the water, and is generally determined by transmitting light through a sample and measuring the intensity of light scattered at 90 degrees to the direction of light transmission (although it is possible to measure turbidity at 180 degrees). The unit of turbidity is the nephelometric turbidity unit (NLU).
It will of course be understood that while the examples above relate to samples which separates into two distinct layers or phases, the same measurement and analysis may be performed on a sample which separates into several different layers or phases, for example a sample taken from a multiphase flow such as a flow of hydrocarbon fluids which contains (at least) natural gas, oil and water, or indeed a sample which separates into different layers or phases where the interface between the layers or phases is not distinct (i.e. where there is an interface layer).
With reference to
Within the sample chamber is a dam 5, which is held in position against an inner surface of the sample chamber 3. The dam prevents fluid communication between inlets 9 and outlets 11, as will be clear from the description of the operation of the sampling apparatus 1 below. The inlets 9 and outlets 11 enable a sample to be drawn into and ejected from the sample chamber 3, respectively. As will be clear, the inlets 9 may serve as outlets and the outlets 11 may serve as inlets depending on the direction in which gate 7 is moved (see below). Although the inlets 9 and outlets 11 are shown as being present only on the cylindrical section 3A of the sample chamber, they may extend down the frusto-conical section 3B and up the bevelled section 3C such that a sample is drawn into the sample chamber 3 through inlets 9 (or outlets 11) which extend the full height of the sample chamber 3.
To draw samples into the sample chamber 3, the apparatus comprises a gate 7 which pivots about a longitudinal axis extending through the sample chamber 3. The gate 7 is reciprocated within the sample chamber 3 by motor 13 via a gear assembly 15. The motor 13, and hence movement of the gate 7, is controlled by gate control electronics 17 which may in turn be controlled by commands or signals received from apparatus control electronics or an external controller (not shown).
Embedded in a sample-facing first surface 5A of the dam 5 is a settlement analyser 51 which in this embodiment extends from the bottom of the dam 5 (and hence the bottom of the sample chamber 3) to the top of the dam 5 (and hence the top of the sample chamber 3). The settlement analyser 51 takes the form of a channel with an array of emitters provided on one inner surface of the channel and an array of detectors provided on an opposing inner surface of the channel, such as illustrated in
In this position, the settlement analyser 51 is exposed to and is therefore able to analyse the contents of the sample chamber 3 (or at least that portion of the contents of the sample chamber with the channel or sample volume of the settlement analyser) according to the above description. A measurement performed immediately or shortly after the sample has been drawn into the sample chamber 3 permits, for example, a determination of the quantity of particles in the completely mixed sample, a determination of MLSS concentration, and/or a turbidity measurement. After a delay, during which the sample settles or separates into component layers, a measurement performed at this time permits determination (for example) of the level/s at which each component settles, the solid volume fraction of particles in the layered fractions, and/or the depth of the interface layer between the fractions. As noted above however there are advantages to performing measurements during the entire settlement period.
It will be understood that as shown in
The dam 5 and/or the gate 7 can be provided with other sensors in addition to the (one or more) settlement analyser(s) 51. Examples of sensors which might be employed include oxygen sensors (for example to measure dissolved oxygen in the sample), temperature sensors, chemical sensors (for example to measure the presence of potassium or ammonium), pH sensors, density sensors, conductivity sensors and salinity sensors. A contact sensor might also be employed to detect when the gate abuts the dam, at which point the motor driving the dam can be automatically stopped.
Reciprocation of the gate 7 back and forward between first and second positions where it abuts first and second faces 5A,5B of the dam 5, provides a mechanism for repeatably and repeatedly drawing samples into the sample chamber 3 and ejecting samples from the sample chamber 3 in an effective and an efficient manner. Whether the settlement analyser 51 is located on the dam 5 or the gate 7, it is envisaged that the action of reciprocating the gate 7 will aid in flushing out the sampling channel of the settlement analyser 51. However, micro-pumps may be provided to flush out the settlement analyser 51 between samples/measurements. Such pumps, or indeed other pumps, may also be used to agitate a captured sample. Such agitation may be used to assist in ejection of the sample. Alternatively, or additionally, the sampling apparatus 1 may be provided with one or more pumps to allow for inoculation of a captured sample with gaseous and/or liquid inoculants.
Alternatively, or in addition, the gate 7 or the dam 5, respectively, can be provided with a web or similar protrusion (not shown) which cooperates with the settlement analyser 51 such that when the dam 5 is in contact with or close to the gate 7, the web is received in the sampling channel of the settlement analyser 51 to aid in removing the sample from the sampling channel. The web may therefore comprise wipers, brushes or the like, that may serve to wipe and/or clean the emitters and detectors of the respective arrays.
The top housing 33 is attached to a post 35 (the full extent of which is not shown) which enables the sampling apparatus 1 to be mounted within, for example, a process or flow. Selection of an appropriate length of post 35 enables the apparatus 1 to be submerged to a predetermined or desired depth within a process or flow, and if provided with a hermetic seal (as is preferred) the apparatus 1 can be left in situ indefinitely. One of the advantages of immersing the apparatus is the removal of the need for trace heating or cooling for electronics (and other components) due to the extremes of summer or winter conditions since it is anticipated that a process or flow may provide acceptable environmental conditions within the operating restrictions of the apparatus.
The post 35 is hollow to enable communication of data to and/or control of the apparatus by an external controller via one or more conduits (not shown). Alternatively the apparatus may communicate with an external controller using wireless communication protocols such as Bluetooth, Wi-Fi, NFC or the like. The hollow post may enable delivery of inoculants to outlets on the dam/gate and/or supply of air or water to micropumps on the dam/gate from an external source.
In combination with a suitable controller, the apparatus 1 may form part of a process or flow (including multiphase flow) monitoring system. Furthermore, the apparatus may be employed to monitor a process or flow by obtaining samples from the process or flow and performing or enabling measurements on those samples. The process or flow may be altered responsive to the measurements made by the apparatus, thus enabling improved performance.
In an alternative embodiment of the invention the settlement analyser may be comprised in an apparatus which, instead of actively drawing samples into and ejecting samples from a sample chamber in which the settlement analyser is situated, receives samples contained within sample containers such as test tubes.
Such an apparatus is illustrated in schematic form in
The use of a sample container 261 which, for example, might be glass or Perspex, introduces a slight complication in that transmission through the sample is now attenuated by the material of the sample container 261. Accordingly, while the sample analysis carried out on the sample can follow the steps outlined above in relation to the settlement analyser 51 shown in and discussed in relation to
The results of the sample analysis, which may include graphical data corresponding to or similar to
The invention provides a settlement analyser and a method of analysing settlement which employs an array of emitters and at least one array of detectors, wherein the settlement analyser is configured to analyse a sample placed or otherwise located between the array of emitters and the at least one array of detectors by sequentially emitting light from the array of emitters, and detecting light which arrives at the at least one array of detectors via the sample volume. Repeating this sequence allows an optical profile of the sample to be determined as a function of time. The sequence may be a linear sequence, or it may be a non-linear sequence, and light from a particular emitter may be detected by several different detectors in order to increase the resolution of the analyser and the method. The analyser and the method may thereby identify the location of boundaries or interfaces between different layers in a sample once settled and during settlement. Furthermore, measurements obtained by the settlement analyser and method may be used to determine one or more properties of the sample, including MLSS concentration, SV30 number and SVI value. In one embodiment one or more settlement analysers may be comprised in an apparatus which may be located in a process or flow and thereby obtain and analyse samples directly from the process or flow, and in another embodiment a stand-alone analyser is able to receive and analyse samples within sample holders.
As may be used herein, the terms bottom, lower, below and the like are descriptive of a feature that is located towards a first end/side of an apparatus, system or component while the terms top, upper, above and the like are descriptive of a feature that is located towards a second, opposing end/side of the apparatus, system or component. Such an apparatus, system or component may be inverted without altering the scope of protection which, as below, is defined by the appended claims.
Throughout the specification, unless the context demands otherwise, the terms “comprise” or “include”, or variations such as “comprises” or “comprising”, “includes” or “including” will be understood to imply the inclusion of a stated integer or group of integers, but not the exclusion of any other integer or group of integers.
The foregoing description of the invention has been presented for the purposes of illustration and description and is not intended to be exhaustive or to limit the invention to the precise form disclosed. The described embodiments were chosen and described in order to best explain the principles of the invention and its practical application to thereby enable others skilled in the art to best utilise the invention in various embodiments and with various modifications as are suited to the particular use contemplated. Therefore, further modifications or improvements may be incorporated without departing from the scope of the invention as defined by the appended claims.
Number | Date | Country | Kind |
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1912817.2 | Sep 2019 | GB | national |
Filing Document | Filing Date | Country | Kind |
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PCT/GB2020/052054 | 8/27/2020 | WO |