Method for calibrating an ultrasonic measuring device intended to analyze a liquid metal.
By generating a standing acoustic wave to normalize probe responses, the method standardizes ultrasonic probe measurements for liquid metal inclusion characterization, addressing probe variability and enhancing inclusion detection consistency.
Patent Information
- Application Number
- FR2024003829
- Authority / Receiving Office
- FR · FR
- Patent Type
- Applications
- Current Assignee / Owner
- Filing Date
- 2024-04-12
- Publication Date
- 2025-10-17
AI Technical Summary
Existing ultrasonic probes for characterizing liquid metal inclusions vary in response due to differences in electronic circuits and materials, making it difficult to apply a consistent correlation curve across probes of identical design.
A method involving the generation of a standing acoustic wave in the liquid metal to normalize the probe response by arranging a sonotrode to emit the wave, detecting reflected waves, calculating a normalization amplitude, and applying a normalization function to standardize the amplitude measurements across probes.
Enables consistent amplitude measurements across different ultrasonic probes, allowing the use of a unified correlation curve for inclusion size estimation, overcoming probe variability and reducing inclusion concentration in the observation field.
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Abstract
Description
Title of the invention: Method for calibrating an ultrasonic measuring device intended to analyze a liquid metal. Technical field
[0001] The technical field of the invention is the characterization, by ultrasound, of a casting of liquid metal, for example a casting of an aluminum alloy. Prior art
[0002] In the field of metal casting, it is necessary to control the quality of the liquid metal, so as to detect inclusions. This is particularly the case for aluminum. Some industries, for example the casing industry, have high requirements regarding the quality of molten aluminum alloys. The quality of the molten metal is determined by a quantity of inclusions present in the metal. These may be traces of gases, oxides, nitrides, carbides, fluorides or borides. Inclusions commonly encountered in molten aluminum are for example A12O3, MgAl2O4, A14C3, MgO, CaO, CaF2, TiB2, TiVB2, SiO2.
[0003] It is possible to monitor, online, the quality of a casting by ultrasonic measurement techniques. According to this type of measurement, an ultrasonic acoustic wave propagates through liquid metal. The acoustic wave propagates through the liquid metal. In the presence of inclusions, a part of the emitted acoustic wave is reflected and can be detected. The reflected or diffracted Fonde amplitude makes it possible to trace back to a size of inclusions in the metal. The ultrasonic technique allows a characterization of a part of the liquid metal, typically 2%.
[0004] Probes for carrying out measurements, by ultrasound, on castings, have been described in patents EP3204764B1, EP3204763B1.
[0005] Document EPI 194772B1 describes a method for calibrating a probe, in which reflectors are placed at the end of rods, the latter being placed in liquid metal. The reflectors can be of different sizes. It is thus possible to establish a correlation between the size of each reflector and the amplitude of the detected acoustic background. Such a method needs to be applied for each probe. In addition, it assumes the placement of calibrated reflectors in a liquid metal, which can be complex.
[0006] Another possibility for estimating the size of inclusions is to use a correlation curve between measurements resulting from an ultrasonic probe and measurements resulting from a method considered as a reference method. The reference method may for example be an analysis method of the “LIMCA” (Liquid Metal Cleanliness Analysis) type, based on an analysis of the electrical resistance of a liquid metal sample. This can also be the method described in EPI 194772B1, using calibrated reflectors. A correlation function can thus be established between the size of inclusions, measured by the reference method, and the amplitude of the ultrasonic signal.
[0007] A difficulty linked to the use of ultrasonic probes is that their response can vary from one probe to another. However, it is difficult to envisage calibrating each probe with a reference method, such as LIMCA or as described in EP1194772B1. Such calibration requires time.
[0008] The variability of the response between two probes, of identical structures, is due to differences which may affect the electronic circuits, or the materials used. Faced with identical inclusions, two different probes, of identical design, can generate detection signals of different amplitudes, due to the variability of the instrument response.
[0009] It is preferable, even necessary, to take such variability into account, for example if one wishes to apply the same correlation curve to measurements resulting from different ultrasonic probes.
[0010] The inventors propose a method allowing for the variability of responses of two different probes to be taken into account. The objective is that two probes, of identical design, generate identical signals, or signals that can be considered as such, in the presence of identical inclusions. Statement of the invention
[0011] A first object of the invention is a method for calibrating an ultrasonic measuring device, the device being intended to characterize a liquid metal, the device comprising: - a measuring transmitter configured to emit an incident ultrasonic wave into the liquid metal; - a receiver configured to detect an ultrasonic wave reflected or diffracted by an inclusion in the liquid metal, following the emission of the incident ultrasonic wave; - a processing unit, configured to determine an amplitude of the detected ultrasonic wave;
[0012] the method being characterized in that it comprises the following steps: a. arrangement of a sonotrode in a liquid metal, and arrangement of the device, such that the measuring transmitter and the receiver are arranged in the liquid metal or facing the liquid metal; b. activation of the sonotrode, during an activation period, so as to generate a standing acoustic wave propagating through the liquid metal; c. power supply to the measuring transmitter, so that the measuring transmitter emits an incident ultrasonic wave propagating in the liquid metal at different calibration times, the calibration times forming a calibration period; d. at each calibration instant, detection, by the receiver, of an ultrasonic wave reflected or diffracted by the liquid metal under the effect of the incident wave, and determination of the amplitude of the ultrasonic wave detected by the receiver; e. calculation of a normalization amplitude as a function of the amplitude measured at each calibration instant. f. calculating a normalization function, configured to normalize each amplitude of an ultrasonic wave detected by the receiver by the normalization amplitude.
[0013] The standing acoustic wave may be an ultrasonic wave.
[0014] The device can be arranged at a distance from the sonotrode of less than 2 meters.
[0015] The frequency of the standing acoustic wave may be different from the frequency of the incident wave.
[0016] The calibration period may be subsequent to the activation period.
[0017] According to one possibility, the sonotrode forms the measuring transmitter. The method is then such that: - during step b), the measuring transmitter emits the standing acoustic wave; - during step c), the measuring transmitter and the receiver of the device are activated, so as to determine the amplitude of the ultrasonic wave detected by the receiver.
[0018] According to one possibility, the calibration period extends for a duration of less than 1s (second).
[0019] According to one possibility, the frequency of the standing acoustic wave, generated during step b), is higher than the frequency of the incident ultrasonic wave emitted during step c).
[0020] According to one possibility: - the frequency of the standing acoustic wave, generated during step b), is different from the frequency of the incident ultrasonic wave emitted during step c). - the calibration period includes all or part of the activation period, all or part of steps b) and c) being implemented simultaneously.
[0021] A second object of the invention is a method for characterizing a liquid metal, the method implementing an ultrasonic measuring device, comprising: - a measuring transmitter configured to emit an incident ultrasonic wave in the liquid metal; a receiver configured to detect an ultrasonic wave reflected or diffracted by an inclusion in the liquid metal, following the emission of the incident ultrasonic wave; a processing unit, configured to determine an amplitude of the detected ultrasonic wave;
[0022]
[0023]
[0024] the method comprising the following steps: (i) arrangement of the device, such that the measuring transmitter and the receiver are arranged in the liquid metal or facing the liquid metal; (ii) powering the measuring transmitter, so that the measuring transmitter emits an incident ultrasonic wave propagating in the liquid metal; (iii) detection, by the receiver, of an ultrasonic wave reflected or diffracted by an inclusion in the liquid metal under the effect of the incident wave; (iv) at a measurement instant, measurement, by the receiver, of an ultrasonic wave reflected or diffracted by an inclusion in the liquid metal under the effect of incident ultrasonic waves, and determination of the amplitude of the ultrasonic wave detected by the receiver at each measurement instant; the method being characterized in that it comprises (v) application of a normalization function to the amplitude determined at the measurement time, the normalization function being defined by a method according to the first subject of the invention According to one possibility: the liquid metal flows along a chute; the transmitter and receiver are positioned facing the chute.
[0025] According to one possibility: the measuring transmitter is coupled to a first waveguide, immersed in the liquid metal; the receiver is coupled to a second waveguide, immersed in the liquid metal.
[0026] A third object of the invention is an ultrasonic measuring device, comprising: a measuring transmitter configured to emit an incident ultrasonic wave into the liquid metal; a receiver configured to detect an ultrasonic wave reflected or diffracted by an inclusion in the liquid metal, following the emission of the incident ultrasonic wave; a processing unit, configured to measure an amplitude of the ultrasonic wave detected by the receiver in different measurement times; - applying a normalization function to each measured amplitude, the normalization function being defined by implementing steps a) to f) of a method according to the first subject of the invention.
[0027] The invention will be better understood upon reading the description of the exemplary embodiments presented in the remainder of the description, in conjunction with the figures listed below. Figures
[0028] [Fig. 1A] represents a first embodiment of a probe allowing implementation of the invention.
[0029] [Fig.1B] represents another embodiment of a probe allowing an implementation of the invention.
[0030] [Fig.2] shows a diagram of acoustic waves detected at a measurement time.
[0031] [Fig.3] schematizes a standing acoustic wave extending through a gutter.
[0032] [Fig.4] represents a correlation curve between detected wave amplitudes and an inclusion dimension.
[0033] [Fig.5] shows schematically the main steps of a method according to the invention.
[0034] [Fig.6A] shows a diagram of a sonotrode immersed in a chute.
[0035] [Fig.6B] shows a temporal evolution of the concentration of inclusions of different sizes in a casting, with and without application of a standing acoustic wave, during a first test.
[0036] [Fig.6C] shows a temporal evolution of the concentration of inclusions larger than 20 pm in a casting, with and without application of a standing acoustic wave, during a second test.
[0037] [Fig.6D] and [Fig.6E] show histograms of the size distribution of inclusions, with and without application of a standing acoustic wave.
[0038] [Fig.6F] shows a temporal evolution of the concentration of inclusions larger than 20 pm in a casting, with and without application of a standing acoustic wave, during a third test.
[0039] [Fig.7A] and [Fig.7B] are images resulting from PODFA (Porous Disk Filtration Analysis) analyses of samples taken from a flow respectively without and with application of a standing acoustic wave.
[0040] [Fig.8A] shows the evolution of a detection signal resulting from the probe during an experimental test.
[0041] [Fig.8B] shows an enlargement of the area boxed in [Fig.8A]. Presentation of specific embodiments
[0042] A first example of an ultrasonic probe has been shown in connection with [Fig. 1A], allowing an implementation of the invention. The probe comprises a measurement transmitter 11 and a receiver 21. In this example, the measurement transmitter 11 and the receiver 21 are formed by the same acoustic transducer. The acoustic transducer is for example a piezoelectric transducer, known to those skilled in the art.
[0043] The transducer is for example a pellet of piezoelectric material emitting an acoustic wave at a frequency of 15 MHz. Generally, the frequency of the emitted acoustic wave is preferably between 1 MHz and 20 MHz.
[0044] The probe is intended for detecting inclusions 4 in a liquid medium 2 to be analyzed, and more precisely in a liquid metal, the metal being for example an aluminum alloy. In [Fig.1A], the dotted horizontal line represents an interface between the liquid metal 2 and an ambient medium 3, the latter being for example air.
[0045] The probe 1 comprises a waveguide 13, intended to be immersed in the liquid metal 2. The waveguide is configured to facilitate propagation of an acoustic wave between the transducer, acting as a transmitter-receiver, and the liquid metal 2. The waveguide 13 is for example formed from a material of the silicon nitride or silicon oxynitride (SiAlON) type, or more generally a material, of the refractory metal or ceramic type, considered to be inert to the liquid metal 2. The use of such a waveguide has been described in EP3204763B1 or in EP1194772B1.
[0046] In [Fig.1A], an ultrasonic field 5 is shown diagrammatically, which corresponds to a part of the liquid metal inspected by the probe 1. When an inclusion 4 crosses the ultrasonic field, a part of the acoustic wave emitted by the measuring transmitter 11 is reflected or diffracted towards the receiver 21. The characteristics of the reflected wave, in particular its amplitude, allow the detection of an inclusion and its characterization, for example an estimation of its size.
[0047] Preferably, the probe may comprise a power emitter 12, configured to emit an acoustic wave of power, i.e. greater than 10W, and preferably greater than 50W or 100W, for example 120W, as described in EP3204764. Indeed, the application of a high-power acoustic wave makes it possible to obtain the wetting of the first waveguide 13 by the liquid metal 2. The power emitter 12 is activated at regular intervals, so as to allow good wetting of the waveguide 13 by the liquid metal 2 to be maintained.
[0048] [Fig.lB] represents a preferred configuration, in which the probe comprises a measuring transmitter 11 and a receiver 21. The measuring transmitter 11 is connected to a first waveguide 13. The receiver 21 is connected to a second waveguide 23, preferably identical to the first waveguide 13 (same material, same dimensions), but distinct from the latter. The length of each waveguide is for example between 10 cm and 50 cm. The first and second waveguides are preferably rectilinear, and extend respectively around a first central axis Al and a second central axis A2. The central axes Al and A2 are intersecting, and inclined relative to each other at an angle a. The angle is for example between 20° and 40° and preferably between 25° and 35°. The angle a is for example equal to 28°. Such a configuration has been described in EP3204764B1.
[0049] In this embodiment, the probe may comprise a first power emitter 12, and a second power emitter 22, as described in connection with the first embodiment. The first and second power emitters are activated periodically, so as to improve the wetting of the first waveguide 13 and the second waveguide 23, respectively, by the liquid metal 2.
[0050] The probe comprises a control unit 31, configured to allow control of the emission of an acoustic wave by the measurement transmitter 11, and to allow control of the emission of a power acoustic wave by the power transmitter 12 when the probe comprises such a transmitter.
[0051] Regarding the acoustic waves emitted by the measuring transmitter 11, they are generally emitted in series. In practice, each series of acoustic waves is emitted by the measuring transmitter 11 at a regular frequency, for example 0.1 Hz. A series comprises at least one acoustic wave, and preferably several successive acoustic waves. Within the same series, the emission frequency of the acoustic waves can be between 100 Hz and 300 Hz, which corresponds to the excitation frequency of the piezoelectric transducer of the measuring transmitter.
[0052] In [Fig. 2], three waves detected by the receiver 21 are shown diagrammatically, following the emission of a series of three waves by the measuring transmitter 11. The bracket indicates that the three waves belong to the same series. In [Fig. 2], the ordinate axis corresponds to the signal S(t) detected by the receiver 21 while the abscissa axis corresponds to time t.
[0053] The probe comprises a processing unit 32, configured to calculate an amplitude of the waves detected by the receiver 21 in response to a series of acoustic waves emitted by the measurement transmitter 11. The calculated amplitude can be an average of the maximum amplitudes of each detected acoustic wave, or the maximum amplitude of all the acoustic waves detected following the emission of a series of waves. Subsequently, the calculated amplitude is noted A(tm). denotes a measurement instant, which corresponds to the detection of a series of acoustic waves by the receiver 21.
[0054] When the amplitude A(tm) crosses a certain threshold, we are in the presence of an inclusion 4 in the liquid metal. The amplitude A(fm) can be used to estimate an inclusion size, from a correlation curve established experimentally, using a reference method, for example the LIMCA method or the method based on the use of calibrated reflectors, these methods being described in connection with the prior art.
[0055] The same correlation curve can be used on different ultrasound probes of identical design, provided that the amplitudes resulting from said ultrasound probes are comparable. However, as previously indicated, it is necessary to take into account the variability of the probes, even if the latter are similar to each other: same dimensions and same materials used.
[0056] The processing unit 32 comprises an amplifier, intended to amplify the signal resulting from the receiver 21, and whose amplification gain Go is generally fixed in the factory, following the manufacture of the probe. The gain is generally not modified during the procedure. It can be subject to an adjustment depending on the conditions of use of the probe.
[0057] The probe 1 is intended to be immersed in a liquid metal 2 flowing from a furnace. For example, the liquid metal flows along a chute. The waveguide(s) of the probe are immersed in the chute.
[0058] For reasons of cost and time, it is not realistic to produce, for each probe, a correlation curve with a reference method. However, it is necessary to take into account the variability of the response of each probe. The inventor proposes a method making it possible to obtain a comparable response for each probe, so as to be able to use a correlation curve as described below, in connection with [Fig.4].
[0059] An important aspect of the invention is to be able to have, within a casting, a liquid metal in which the concentration of inclusions is controlled, in order to carry out a so-called calibration measurement using an ultrasonic probe. The underlying idea is that for the same concentration of inclusions, the measurement amplitude must be the same, regardless of the probe used.
[0060] However, the concentration of inclusions in a casting varies in time and space. In order to obtain a controlled concentration of inclusions, the casting is subjected to a standing acoustic wave, at at least one point of the casting. The inclusions are then placed in an acoustic pressure field, and undergo a force, called acoustic force, which can cause a displacement of said inclusions. The inclusions can concentrate in the pressure nodes, that is to say the zones in which the amplitude of the pressure wave is minimal, or in the pressure antinodes, that is to say the zones of the sample in which the amplitude of the pressure wave is maximal. It has also been observed that the inclusions concentrate at the interfaces, whether these are the walls delimiting the chute or the free surface of the liquid metal. Thus, the use of an acoustic wave allows a placement of inclusions, without physical contact, so as to impoverish the observation field of the probe, that is to say reduce the quantity of inclusions present in the observation field.
[0061] The invention is based on the generation of a standing acoustic wave at certain points of the casting, upstream and / or downstream, or at the level of a probe. According to the principles of acoustophoresis, the standing acoustic wave makes it possible to move and / or retain inclusions flowing in the casting, outside the field of observation of the probe 1. Thus, the field of observation of the probe can be considered as devoid of inclusions.
[0062] According to one possibility, the sonotrode is arranged at a distance from the probe (or more precisely from the field of observation of the probe), upstream or downstream of the probe, the upstream and downstream being defined relative to the flow of the liquid metal. The inclusions are then trapped, in particular at the free interface (liquid metal / air interface) or at the walls of the chute. The distance between the probe and the sonotrode is then preferably greater than 10 cm, and for example between 30 cm and 2 m. This distance is adjusted by a person skilled in the art, so that it is sufficient so that the standing acoustic wave is not detected by the probe, while being sufficiently close, so that the filtration effect exerted by the standing wave is used. In Figure 3, a standing acoustic wave H7 extending perpendicularly to a flow direction of a stream of liquid metal 2 flowing in a chute G is shown.The inclusions move towards the free interface 2' (liquid metal / air interface) or towards the wall 6 of the chute.
[0063] According to another possibility, the sonotrode is formed by the emitter 11 of the probe. In this case, the emission of the standing acoustic wave by the emitter induces a displacement of the inclusions outside the field of observation, at the level of the free interface or the walls of the chute.
[0064] Whatever the embodiment, the standing acoustic wave is emitted at a high frequency, typically greater than 10 KHz, or 20 KHz if it is desired to limit noise pollution. It is believed that this is more effective with regard to small inclusions. In addition, the application of a standing acoustic wave in the ultrasonic domain makes it possible to limit noise pollution.
[0065] The standing acoustic wave W generated upstream of the probe 1 acts as a filter, making it possible to move and / or maintain the inclusions outside the field of observation. Thus, in the field of observation, the quality of the liquid metal can be considered as controlled, in the sense that the metal can be considered as free of inclusions, or sufficiently depleted in inclusions.
[0066] An objective of the invention is to take advantage of the filter effect conferred by the standing acoustic wave, so as to carry out a calibration of the probe, on a portion of the casting considered clean, or at least of controlled inclusion quality.
[0067] The sonotrode, whether it is the same as the measuring transmitter or is different from the latter, is configured to emit the standing acoustic wave during an activation period. Ta. The activation period Ta can last a few seconds or a few minutes.
[0068] According to one possibility, the activation period is followed by a calibration period Te, during which stationary acoustic wave is preferably not emitted, so that it is not detected by the probe receiver. The calibration period Te is sufficiently close to the activation period Ta so that it can be considered that during the calibration period, the effect of the stationary acoustic wave on the liquid metal remains. Thus, during the calibration period, the observation field of the probe is considered to be free of inclusions, or sufficiently depleted in inclusions.
[0069] It is understood that it is preferable for the calibration period to be as close as possible to the activation period, so as to take advantage of the arrangement of the inclusions, outside the field of observation of the probe, under the effect of stationary acoustic background emitted during the activation period.
[0070] According to another possibility, the frequency of the stationary acoustic background is sufficiently different from the emission frequency of the transmitter 11 of the probe, so that the influence of the stationary acoustic background can be considered negligible on the acoustic background detected by the receiver of the probe.
[0071] Whatever the embodiment, during the calibration, the device to be calibrated is immersed in the liquid metal and a measurement is carried out at one or more calibration instants L-. At each calibration instant there corresponds a calibration amplitude A(LL) which corresponds to an amplitude of the signal detected by the probe at the calibration instant. From the calibration amplitude or amplitudes A(l), a normalization amplitude, denoted AN, is defined which corresponds to the average or the median of the calibration amplitudes A(tc).
[0072] The duration of the calibration period Ta depends on the experimental conditions. It can last from a few ms to a few hundred ms, or even a few seconds.
[0073] After the normalization amplitude AN has been determined, each amplitude A(tm) resulting from the probe, at a measurement time 6«, can be normalized, by a normalization function / , such that: = = ^x««) Or : / corresponds to the normalization function. • A ( tm ) is the normalized amplitude • N can be for example 20. In this case, the normalized amplitude f ( A(tn^) is expressed in %. The value of 20% corresponds to a casting considered as clean.
[0074] Once the normalization function has been defined for the probe, the latter can be used in the same way as a reference probe, whose response is known.
[0075] An advantage of the method is that the value of the normalized amplitude A( corresponding to the normalization value N, for example 20%, represents a clean casting, regardless of the probe used. Normalization makes it possible to overcome the variability affecting the probes: the normalized amplitudes A( of the different probes are comparable with each other, because the normalization amplitude AN is established, for each probe, under comparable conditions, in this case in the presence of a liquid metal considered to be clean.
[0076] Standardization assumes that it is accepted that the liquid metal, considered clean, that is to say free from inclusion, or sufficiently depleted, generates acoustic waves whose amplitude is assimilated to noise. This amplitude corresponds to the normalization amplitude Ay.
[0077] Normalization makes it possible to use a correlation curve as shown diagrammatically in Figure 4. The correlation curve is established experimentally with a reference probe, after applying the normalization function determined for said reference probe. Thus, the ordinate axis corresponds to f ( Ac ), where Ac corresponds to measured amplitudes correlated with known inclusion dimensions. The abscissa axis corresponds to a size of the inclusions, for example the diameter, measured by the reference method. The curve in [Fig.4] is a response function established for the reference probe: it establishes a correlation between the normalized measurements, resulting from the reference probe, and known inclusion dimensions, established by a reference method, for example the LIMCA method.
[0078] The use of the normalization function makes it possible to recalibrate the response of each probe, so that the response of each probe is comparable to the response of the reference probe.
[0079] The main steps of the invention are now described, shown diagrammatically in [Fig.5].
[0080] Step 100: Generation of a standing acoustic wave during a period activation. During this step, a sonotrode S is used to generate the standing acoustic wave W, propagating through the liquid metal. The sonotrode S may be different from the emitter 11, in which case it is arranged downstream or upstream of the latter. According to one possibility, the sonotrode S is merged with the emitter 11. When the frequency of the standing acoustic wave is sufficiently different from the frequency of the acoustic wave emitted by the probe emitter, the activation period Ta may be confused with all or part of the calibration period Te. When the standing acoustic wave is likely to be confused with an acoustic wave reflected by the liquid metal, in response to an acoustic wave emitted by the probe emitter, the calibration period Te is consecutive to the activation period Ta. The time interval between the calibration period and the activation period is then as small as possible.
[0081] Step 110: Determination of the normalization amplitude during the calibration period. During this step, a probe, as described in connection with figures 1A and 1B, is arranged downstream of the sonotrode S, so as to carry out at least one measurement of one or more calibration amplitudes A(l), in one or more calibration instants L. From the calibration amplitude A(l) or from an average (or a median, or other statistical quantity) of the measurements A(fc), the normalization amplitude AN is determined.
[0082] Step 120: Determination of the normalization function From the normalization amplitude A^, the normalization function / of the probe is defined according to (1). Steps 110 and 120 are implemented by the processing unit 32.
[0083] Step 130: Taking measurements After the probe normalization function has been defined, the probe can be used to perform measurements at different measurement times 0«. Each measurement time corresponds to a measurement amplitude A(tm), as described in connection with [Fig.2].
[0084] Step 140: Normalization In this step, the measurement amplitude is normalized according to (1) using the normalization function resulting from step 120.
[0085] Steps 100 to 120 are preferably implemented for probes of identical design. This makes it possible to obtain a normalization function, associated with each probe. The normalized measurements of each probe are then considered to be comparable, the variability of each probe being corrected by the normalization function defined for each of them.
[0086] A correlation curve can be established by comparing measurements, from a reference method (for example LIMCA) with the resulting normalized amplitudes of a probe considered as a reference probe. Such a curve can then be used for the normalized amplitudes of all probes, of similar design to the reference probe. Experimental tests
[0087] The inventors tested the trapping of inclusions by acoustophoresis in a chute. They placed a sonotrode in the center of a chute: see [Fig.6A]. The emission power was 100 W. Relative to [Fig.6A], the dimensions are, in mm: PI = 182, P2 = 166, L1 = 55, L2 = 146.
[0088] Downstream of the probe, a sample of the casting was taken, at a distance of 70 cm from the sonotrode. The sample was subject to a LIMCA type measurement. [Fig.6B] represents a concentration of inclusions (y-axis - number of inclusions, unit thousands per Kg), as a function of time (x-axis: minutes), for different sizes of inclusions (diameters 20 pm; 40 pm; 60 pm; 80 pm). The sonotrode S was activated between t = 40 min and 50 min. It is observed that the concentration of detected particles decreases significantly during the activation of the sonotrode. The concentration of inclusions measured by LIMCA is representative of the inclusionary quality of the casting downstream of the sonotrode. Sonotrode activation is accompanied by an improvement in inclusion quality, for all inclusion sizes. It appears that small inclusions (20 pm) are less sensitive to acoustophoresis.
[0089] During a second test, the sonotrode was activated several times. The concentration of inclusions of size 20 pm downstream of the sonotrode was measured by LIMCA. [Fig.6C] represents a concentration of inclusions of size 20 pm (y-axis - number of inclusions, unit thousands per kg), for different measurement points distributed in chronological order. The sonotrode was activated between measurement points 43 - 47, 53 - 57. Between measurement points 43 and 47, the power of the sonotrode was increased to 40% of the maximum power. Between measurement points 53 and 57, the power of the sonotrode was increased to 60% of the maximum power. It is also observed that the actuation of the sonotrode, for different power levels, makes it possible to reduce the concentration of inclusions downstream of the sonotrode.
[0090] Figures 6D and 6E show the concentrations (y-axis - per thousand inclusions per kg of metal) of inclusions classified by size (x-axis - unit pm), respectively with (histogram a - black) and without (histogram b - gray) application of a transverse acoustic wave. In Figures 6D and 6E, the power of the transverse acoustic wave was 40% and 60% of the maximum power. It is observed that the effect of the transverse acoustic wave is all the more important as the size of the inclusions is large, which is consistent with the observations in connection with [Fig.6B].
[0091] During a third test, measurements of the inclusion quality were carried out by LIMCA as a function of time, and this for two castings, at the furnace outlet: during a first casting, no sonotrode was used. During a second casting, a sonotrode was used, immersed in the casting, upstream (approximately 1 m) of the area sampled for the LIMCA measurements. [Fig.6F] represents the concentrations of inclusions larger than 20 pm measured (y-axis - thousands of inclusions per kg) as a function of time, for each casting. For both castings, a progressive decrease in the concentration of inclusions as a function of time is observed. It is observed that whatever the instant of measurement, the application of ultrasound through the casting allows a significant reduction in the concentration of inclusions.
[0092] In [Fig.6F], the points correspond to the measurements taken. A polynomial interpolation of the measurements was carried out for each of these castings, which makes it possible to obtain a continuous curve for each casting: curve a: without ultrasound - curve b: with ultrasound.
[0093] The case shown in [Fig.6F] corresponds to an improvement in the inclusion quality of the metal as a function of time. The acoustophoresis effect is particularly noticeable at the start of casting, when the metal is rich in inclusions.
[0094] During a series of tests, samples of liquid aluminum were taken during a standard casting, i.e. without the application of ultrasound, and during a test casting, downstream of a sonotrode as previously described. The samples were analyzed by a PoDFA analyzer (Porous Disk Filtration Analysis). [Fig.7A] and [Fig.7B] show metallography images resulting from the PoDFA analysis for the standard casting and the test casting respectively. The comparison between the two figures shows that the application of ultrasound significantly improves the inclusion state of the aluminum: there are significantly fewer oxide films on the test casting.
[0095] The experimental tests described in connection with Figures 6A to 6F and 7A to 7B confirm that the application of an ultrasonic wave makes it possible to obtain a casting in which the concentration of inclusions is limited. The invention is based on the hypothesis that whatever the casting, downstream of a standing acoustic wave, propagating transversely to the flow of the casting, the inclusion quality of a casting is comparable. Thus, downstream of the acoustophoresis acoustic wave, the amplitude of an ultrasonic wave reflected or diffracted by the metal makes it possible to carry out an amplitude adjustment, as described in connection with expression (1).
[0096] During a series of tests, a probe as described in connection with [Fig.lB] was implemented. The transmitter 11 was used as a sonotrode producing a standing acoustic wave. [Fig.8A] shows a time-dependent evolution of the amplitude of waves detected by the receiver 21 of the probe. During an activation period Ta, the standing acoustic wave was emitted at high power, in order to increase the wettability of each waveguide with respect to ultrasound. This also made it possible to impoverish the observation field of the probe by moving the inclusions towards the free surface and / or towards the walls of the chute. During the activation period, the receiver was not used, which explains why the detected amplitude is zero during the activation period.
[0097] Following the activation period, the transmitter 11a emitted an incident acoustic wave at an emission power compatible with the use of the receiver 21 of the probe. [Fig.8B] shows a detail of [Fig.8A]. It can be seen that following the activation period Ta, the measured amplitude is relatively low, due to the depletion of the observation field in inclusions resulting from the activation period. The first moments following the activation period form a calibration period Te, during which the amplitude of the pulses measured by the receiver is considered to be representative of a clean metal. In this example, the calibration period lasts 100 ms.
[0098] The invention can be applied by implementing ultrasonic measuring devices of the same type, that is to say having the same structure, the variability being due to the differences affecting the components of each device. Standardization makes it possible to limit the variability of the response between ultrasonic measuring devices of the same type.
Claims
Claims
1. Method for calibrating an ultrasonic measuring device (1), the device being intended to characterize a liquid metal, the device comprising: - a measuring transmitter (11) configured to emit an incident ultrasonic wave into the liquid metal; - a receiver (21) configured to detect an ultrasonic wave reflected or diffracted by an inclusion in the liquid metal, following the emission of the incident ultrasonic wave; - a processing unit (32), configured to determine an amplitude of the detected ultrasonic wave; the method being characterized in that it comprises the following steps: a. arrangement of a sonotrode (S) in a liquid metal (2), and arrangement of the device (1), such that the measuring transmitter and the receiver are arranged in the liquid metal or facing the liquid metal; b. activation of the sonotrode, during an activation period (Ta), so as to generate a standing acoustic wave propagating through the liquid metal; c. power supply of the measuring transmitter (11), so that the measuring transmitter emits an incident ultrasonic wave propagating in the liquid metal at different calibration times (tc), the calibration times forming a calibration period (Tc); d. at each calibration instant, detection, by the receiver, of an ultrasonic wave reflected or diffracted by the liquid metal under the effect of the incident wave, and determination of the amplitude (A( / c)) of the ultrasonic wave detected by the receiver; e. calculation of a normalization amplitude (AN) as a function of the amplitude measured at each calibration instant. f. calculating a normalization function ( / ), configured to normalize each amplitude of an ultrasonic wave detected by the receiver by the normalization amplitude.
2. The method of claim 1, wherein the stationary acoustic wave is an ultrasonic wave.
3. A method according to any preceding claim, wherein the device is arranged at a distance from the sonotrode of less than 2 meters.
4. A method according to any preceding claim, wherein the frequency of the standing acoustic wave is different from the frequency of the incident wave.
5. A method according to any preceding claim, wherein the calibration period is subsequent to the activation period.
6. Method according to claim 5 in which the sonotrode forms the measuring transmitter, the method being such that: - during step b), the measuring transmitter emits the standing acoustic wave; - during step c), the measuring transmitter and the receiver of the device are activated, so as to determine the amplitude (A( / c)) of the ultrasonic wave detected by the receiver.
7. The method of claim 6, wherein the calibration period extends for a duration of less than 1s.
8. A method according to any preceding claim, wherein the frequency of the standing acoustic wave generated in step b) is greater than the frequency of the incident ultrasonic wave emitted in step c).
9. Method according to any one of claims 1 to 4, in which: - the frequency of the standing acoustic wave, generated during step b), is different from the frequency of the incident ultrasonic wave emitted during step c). - the calibration period comprises all or part of the activation period, all or part of steps b) and c) being implemented simultaneously.
10. Method for characterizing a liquid metal, the method implementing an ultrasonic measuring device (1), comprising: - a measuring transmitter (11) configured to emit an incident ultrasonic wave into the liquid metal; - a receiver (21) configured to detect an ultrasonic wave reflected or diffracted by an inclusion in the liquid metal, following the emission of the incident ultrasonic wave; - a processing unit, configured to determine an amplitude of the detected ultrasonic wave; the method comprising the following steps: - (i) arrangement of the device (1), such that the transmitter of measurement and the receiver are arranged in the liquid metal or facing the liquid metal; - (ii) powering the measuring transmitter, so that the measuring transmitter emits an incident ultrasonic wave propagating in the liquid metal; - (iii) detection, by the receiver, of an ultrasonic wave reflected or diffracted by an inclusion in the liquid metal under the effect of the incident wave; - (iv) at a measurement instant, measurement, by the receiver, of an ultrasonic wave reflected or diffracted by an inclusion in the liquid metal under the effect of the incident ultrasonic wave, and determination of the amplitude (A(f„,)) of the ultrasonic wave detected by the receiver at each measurement instant; the method being characterized in that it comprises - (v) application of a normalization function to the amplitude determined at the measurement time, the normalization function being defined by a method according to any one of claims 1 to 9.
11. The method of claim 10, wherein - the liquid metal flows along a chute; - the transmitter and receiver are positioned facing the chute.
12. A method according to any one of claims 10 or 11, wherein the measuring transmitter is coupled to a first waveguide (13), immersed in the liquid metal; - the receiver is coupled to a second waveguide (23), immersed in the liquid metal.
13. Ultrasonic measuring device, comprising: - a measuring transmitter (11) configured to emit an incident ultrasonic wave into the liquid metal; - a receiver (21) configured to detect an ultrasonic wave reflected or diffracted by an inclusion in the liquid metal, following the emission of the incident ultrasonic wave; - a processing unit (32), configured to - measure an amplitude (A(rm)) of the ultrasonic wave detected by the receiver at different measurement times (?™); - apply a normalization function to each measured amplitude, the normalization function being defined by implementing steps a) to f) of a method according to any one of claims 1 to 9.
Citation Information
Patent Citations
Method for wetting a sonotrode and sonotrode
EP3204763B1
Method for inspecting a liquid metal by ultrasounds
EP3204764A1
Improved method and device for counting inclusions in a liquid metal bath with ultrasounds
EP1194772B1
Method for inspecting a liquid metal by ultrasounds
EP3204764B1
Method, device and use for the device for quantitatively determining the concentration or particle size of a component of a heterogeneous material mixture
US20190145939A1
