WO1999018430A1 - Electrochemical sensors - Google Patents

Electrochemical sensors Download PDF

Info

Publication number
WO1999018430A1
WO1999018430A1 PCT/GB1998/002967 GB9802967W WO9918430A1 WO 1999018430 A1 WO1999018430 A1 WO 1999018430A1 GB 9802967 W GB9802967 W GB 9802967W WO 9918430 A1 WO9918430 A1 WO 9918430A1
Authority
WO
WIPO (PCT)
Prior art keywords
sensor
test
frequency
voltage
alternating voltage
Prior art date
Application number
PCT/GB1998/002967
Other languages
English (en)
French (fr)
Inventor
Lothfi Makadmini
Michael Horn
Hans-Rolf Tränkler
Original Assignee
City Technology Limited
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by City Technology Limited filed Critical City Technology Limited
Priority to AU93564/98A priority Critical patent/AU9356498A/en
Publication of WO1999018430A1 publication Critical patent/WO1999018430A1/en

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/416Systems
    • G01N27/4163Systems checking the operation of, or calibrating, the measuring apparatus

Definitions

  • This invention relates to electrochemical sensors.
  • an electrochemical sensor in particular an amperometric sensor, which has a test electrode, a reference electrode, an electrolyte and a counter electrode
  • the counter electrode is supplied by an input alternating voltage at a given frequency, and a test voltage prevailing at the test electrode is evaluated.
  • the sensor concerned is an amperometric gas sensor, in which the gas to be detected initiates an electrochemical reaction and thereby generates an electric current.
  • the sensor has, among other things, a counter electrode and a test electrode to which the electronic current generated flows.
  • the electronic current is roughly proportional to the concentration of the gas under test.
  • the electronic current is evaluated by usual means using an earthed load resistance connected to the test electrode, and appropriate signal evaluation or processing equipment.
  • the sensor is fitted with a reference electrode which acts to stabilise the potential of the test electrode.
  • a so-called potentiostat is used for this purpose. Its input is connected to the reference electrode, and the counter electrode to its output. A further input to the potentiostat is linked to an earthed voltage divider, over which a standard voltage can be set up. The standard voltage is dependant on the gas to be measured and can, for example, with carbon monoxide also be zero.
  • Impedance measurements are used for function monitoring of the sensor.
  • an alternating voltage is superimposed over the standard voltage, which then contributes an alternating component to the test voltage at the load resistance.
  • This alternating component is processed further by the signal evaluation so that certain signal patterns can demonstrate a sensor failure.
  • the problem of such a processing is that the alternating component is usually dependant on the concentration of the gas passing through the sensor.
  • Preferred embodiments of the present invention aim to improve the way of operating such a sensor, and especially function monitoring procedures.
  • a method of operating an electrochemical gas sensor which is fitted with a test electrode, a reference electrode and a counter electrode, wherein the counter electrode is supplied with an input alternating voltage of frequency ⁇ , and a test voltage prevailing at the test electrode is processed to provide information representative of the condition of the sensor.
  • the senor is an amperometric sensor.
  • the prevailing test voltage is measured at two successive time intervals, at a given frequency of the input alternating voltage, and the values of the test voltage obtained at said successive time intervals are compared to one another.
  • the frequency of the input alternating voltage is selected such that the phase displacement between the input alternating voltage and the test voltage is small or substantially zero.
  • selection of said frequency of the input alternating voltage, at which the phase displacement is small or substantially zero is effected by first applying a lower frequency and then raising this frequency.
  • said lower frequency is a frequency of a few Hertz.
  • the frequency of the input alternating voltage is controlled by a signal processor.
  • an electrochemical gas sensor and control circuit therefor wherein the sensor comprises a test electrode, a reference electrode and a counter electrode, and the control circuit comprises an alternating voltage source arranged to supply the counter electrode with an alternating voltage of frequency ⁇ , and signal processing means arranged to receive a test voltage prevailing at the test electrode and to process the test voltage (UL) to provide information representative of the condition of the sensor.
  • such an electrochemical gas sensor and control circuit is arranged to perform a method according to any of the preceding aspects of the invention.
  • An electrochemical gas sensor and control circuit as above may further comprise any one or more of the features disclosed in the accompanying specification, claims, abstract and/or drawings, in any combination.
  • the test voltage is used to monitor a cell constant of the sensor.
  • a cell constant is roughly inversely proportional to the electrochemically active area of the sensor - that is, it represents the surface area of electrode that is available for electrochemical reaction. Changes in the active area of the sensor, for example, by ageing phenomena, can be recognised by the inversely proportional changes in the cell constant, and taken into consideration.
  • Monitoring the cell constant of the sensor it is therefore possible to control the functioning capability of the sensor, especially with reference to changes in the electrochemically active area of the sensor, and, if necessary, warn the user. This constitutes a significant improvement in function monitoring of the sensor.
  • the input alternating voltages of the prevailing test voltages at a given frequency are measured one after the other at two given time intervals, and compared with one another.
  • This comparison of two test voltages makes it possible to monitor the cell constant.
  • the first measurement of the test voltage is carried out at the start of operating the sensor, that is, when the sensor is pristine. This measured value is stored. The values measured during the sensor's operation can be compared to the stored initial value.
  • Differences or quotients can demonstrate changes in the cell constant, and therefore a change in the electrochemically active area of the sensor.
  • An advantageous further development of an embodiment of the invention selects the frequency of the input alternating voltage in such a way that a phase displacement between the input alternating voltage and the test voltage is small or around zero.
  • This limiting of the frequency of the input alternating voltage makes it possible for the test voltage to be independent of the concentration of the gas activating the sensor. In this way the test voltage generated at this frequency can be used to monitor the functioning of the sensor.
  • the independence of the test voltage from the concentration is achieved in that, at a smallest possible phase displacement between the input alternating voltage and the test voltage, two further factors are no longer involved. These are the concentration-dependent double layer capacity of the electrolyte, and the equally concentration-dependent double layer resistance.
  • the test voltage is therefore essentially only still dependent on the electrolyte resistance.
  • the specific electrolyte resistance is concentration dependant and roughly constant with time, so that electrolyte resistance is proportional to cell constant, and therefore roughly inversely proportional to the electrochemically active area. Therefore a change in the electrolyte resistance is of equal significance to a change in cell constant, as well as a change in the electrochemically active area. This latter change can be used to interpret the functioning capability of the sensor.
  • An advantageous further development of an embodiment of the invention involves the initial application of a low frequency, especially a frequency of a few Hertz. This is then increased as part of the procedure to apply an input alternating voltage in which the phase displacement is small. This allows a simple, yet effective way to find and set up a frequency at which the phase displacement between the input alternating voltage and the test voltage is small, or preferably nearly zero. It is feasible that finding the frequency at which phase displacement is sufficiently small, can be undertaken by a maintenance operator.
  • An advantageous embodiment of the invention allows the frequency of the input alternating voltage to be set up by the signal processing or evaluation. This means that the frequency at which the phase displacement is small is determined automatically by the signal evaluation.
  • the signal evaluation therefore affects the alternating voltage source that generates the input alternating voltage in such a way, that it just sets up a low frequency and then raises the frequency.
  • the signal evaluation monitors the phase displacement between the input alternating voltage and the test voltage, and selects that frequency for the input alternating voltage at which the phase displacement is small or nearly zero.
  • a fully automatic monitoring of the sensor is possible by this means, for it provides an automatic check on the functioning capability of the sensor.
  • An advantageous further development of an embodiment of the invention allows the frequency of the input alternating voltage at which the phase displacement is small to be set up when the sensor starts operating, and be subsequently maintained. Further, at this frequency, the impedance and the alternating component of the test voltage, respectively, are determined. This allows a later failure of the sensor to be recognised according to this embodiment of the invention.
  • the given frequency is determined, especially automatically, and for example, stored.
  • the test voltage and impedance, respectively are obtained and e.g. stored.
  • the time-and-incident-dependent behaviour of the sensor can again be monitored by using an input alternating voltage at the given frequency, and the test voltage and impedance, respectively point to a change in the sensor.
  • the changes in test voltage and impedance, respectively can be used in conjunction with a predetermined threshold value to demonstrate a sensor failure.
  • a defect due e.g. to ageing phenomena or even total failure of the sensor, can be detected reliably in this way, automatically and at no great expense.
  • a maintenance operator could be taught the procedure.
  • An advantageous further development of an embodiment of the invention uses the direct component of the test voltage at the frequency of the input alternating voltage where the phase displacement is small, as output signal for the concentration of the gas activating the sensor.
  • This output signal is, however, still dependent on changes in the sensor, especially from ageing phenomena of the sensor.
  • An especially advantageous embodiment of the invention uses the direct component of the test voltage and the rectified alternating component of the test voltage multiplied together and bound into one signal. In this way it is possible to make the output signal for the concentration of gas activating the sensor independent of ageing and similar phenomena. In particular, changes in the electrochemically active area of the sensor can be monitored continuously by multiplication approaches, and their effects on sensitivity corrected. This quoted multiplicative linking is independent of the characteristic output signal that monitors the sensor's functioning capability. In particular, the output signal generated by the concentration of gas activating the sensor can still be present even when the output signal for the sensor's functioning ability is not being generated.
  • the signal generated at the frequency of the input alternating voltage at which the phase displacement is small is used as a corrected output signal for the concentration of gas activating the sensor.
  • the corrected output signal gives the user information which is corrected for dependence on the size of the electrochemically active area of the sensor. This means that any changes in active area do not lead to a falsification in the corrected output signal.
  • the quoted correction is carried out automatically and permanently, thus providing a so-called online correction.
  • the corrected output signal gives the user information on the concentration of gas activating the sensor, which continuously and automatically equalises and corrects for possible ageing or other phenomena affecting the sensor. Further, the previously mentioned aim of preferred embodiments of the invention is met by an electrical circuit in which the alternating voltage source and the signal evaluation or processing are linked.
  • the coupling according to this embodiment of the invention of the alternating voltage source into the signal processing or evaluation enables the frequency of the input alternating voltage generated by the alternating voltage source to be set in such a way that the phase displacement between the input alternating voltage and the test voltage of the signal evaluation is small or nearly zero.
  • Figure 1 is a circuit diagram of a model example of an electrical circuit according to an embodiment of the invention.
  • Figure 2 is a circuit diagram showing part of the model of Figure 1 in greater detail.
  • FIG 1 shows an electrical circuit 1 for an electrochemical sensor 2.
  • Sensor 2 is an amperometric gas sensor which has a test electrode S (also called sensing-electrode), a reference electrode R and a counter electrode C.
  • Sensor 2 is suitable for determining the concentration of a gas in air.
  • the gas initiates an electrochemical reaction in sensor 2 that results in an electronic current flowing to the test electrode S. This electronic current is roughly proportional to the concentration of the gas to be measured.
  • the gas working on sensor 2 is presented in Figure 1 by an arrow, and the concentration of the gas is designated "x".
  • test electrode S of sensor 2 is connected to earth via a load resistance 3.
  • the electric current generated by the test gas flows from test electrode S over the load resistance 3 to earth, and thereby generates a test voltage UL at the load resistance 3.
  • Circuit 1 is fitted with a potentiostat 4, which stabilises the potential of the test electrode.
  • the potentiostat 4 comprises an operational amplifier
  • the inverting input 8 of the operational amplifier 5 is connected to the reference electrode R of sensor 2.
  • the non-inverting input 9 of the operational amplifier 5 is connected to earth via a direct voltage source 10 and an alternating voltage source 11.
  • the direct voltage source 10 serves to set up a standard voltage US.
  • the direct voltage source 10 can be a voltage divider, connected in parallel to a direct voltage supply, with the standard voltage US being taken from roughly the middle of its range.
  • the operational amplifier 5 acts on the counter electrode C in such a way that the voltage difference between its inverting and non-inverting inputs 8,9, remains about zero. Thereby, the operational amplifier 5 acting via the counter electrode always sets up approximately the standard voltage US at the reference electrode R. This results in the reference electrode R, and finally also the test electrode S, remaining at a nearly constant voltage. Sensor 2 is thereby set over potentiostat 4 to a working point determined by the standard voltage US.
  • the alternating voltage source 11 generates an input alternating voltage UZ, with a frequency ⁇ , which acts on sensor 2 via the non- inverting input 9 of the operational amplifier. 5.
  • the input alternating voltage UZ is, for example, principally a sinewave, rectangular or squarewave voltage.
  • the test electrode S is connected to a signal processor or signal evaluation unit 12. This applies the test voltage UL to the signal processor 12. Further, the signal processor 12 is connected by a connection 13 to the alternating voltage source 11. This connection 13 allows signals to be passed in both directions. The signal processor 12 generates a signal S that provides information representative of the condition or functioning capability of sensor 2.
  • the monitoring of function capability of sensor 2 is carried out by an impedance measurement.
  • the input alternating voltage UZ enables an impedance Z for sensor 2 to be measured by the signal processor 12.
  • This impedance Z enables the signal processor 12 to provide information on the electrochemically active area of sensor 2, and thereby on its condition or functioning capability.
  • the frequency ⁇ of the input alternating voltage UZ from the signal processor 12 is first set at a low value, via connection 13.
  • the frequency ⁇ comprises several Hertz.
  • the test voltage UL is obtained from the signal processor 12.
  • the signal processor 12 compares the phase of the input alternating voltage UZ with the test voltage UL. If these two phases show a large phase displacement, the signal processor 12 increases the frequency ⁇ of the input alternating voltage UZ and again compares the phases of the two above- mentioned signals. This is repeated until the phase displacement between the input alternating voltage UZ and the test voltage UL is small. In particular, this sequence is repeated until the phase displacement is nearly zero or roughly zero.
  • the frequency ⁇ z that can be set by the signal processor 12 for the input alternating voltage UZ can ensure the phase displacement between the input alternating voltage UZ and the test voltage UL is small or roughly at zero.
  • the electrolyte resistance RE is independent of the concentration X of the gas activating the sensor 2.
  • the electrolytic resistance RE is however, proportional to the so-called cell constant C, which in its turn is roughly universally proportional to the electrochemically active area of sensor 2. Therefore, the impedance Z over the electrolyte resistance RE is a measure of the magnitude of the electrochemically active area of sensor 2. If the impedance Z of sensor 2 changes, this means that the electrochemically active area of sensor 2 has changed also.
  • the frequency ⁇ z is determined by the signal processor 12 when the sensor 2 is first taken into service. This frequency ⁇ z is stored by the signal processor 12. Further, the signal processor 12 also measures and stores the impedance ZO and the test voltage ULO at this frequency.
  • the impedance Zi and the test voltage ULi at the given frequency ⁇ z are again measured by the signal processor 12. It is likewise possible that this new measurement can be carried out by an operator over an appropriate interface, and executed by the signal processor 12. It is also possible to carry out the new measurement in some other way and in other eventualities. In every case the measured impedance Zi and test voltage ULi of the new measurement on sensor 2 will be stored by the signal processor 12. The signal processor 12 then compares the impedance ZO and test voltage ULO of sensor 2 measurement at the start of the sensor's use, with impedance Zi and test voltage ULi, respectively, measured later.
  • the signal processor 12 then registers the sensor's failure via signal S.
  • the signal processor 12 may generate a signal Y, in which the test voltage UL is multiplied with the value of impedance Z of sensor 2.
  • This product represents a signal free from changes in the electrochemically active area. This signal can be used to measure the gas concentration X until the signal S from the signal evaluation registers the failure of sensor 2.
  • Figure 2 represents that part of electrical circuit 1 which can, among other things, be used to carry out the comparison described above.
  • the part of circuit 1 shown in Figure 2 is a part of the signal processor 12.
  • the test voltage UL activates an amplifier 14. Because of the direct voltage source 10 and the alternating voltage source 11, the output signal of the amplifier 14 shows both a direct component ug and an alternating component uw. Both components are fed to a high pass filter 15 which separates the alternating component uw and passes it on to a rectifier 16 and a following low pass filter 17. The output signal of the low pass filter 17 is fed to a comparator 18, which compares this output signal ue with a signal ud.
  • the signal ud represents the threshold value at which the signal processor 12, as described, registers the failure of sensor 2.
  • the signal ud for example, can be a given factor, e.g. 250% of the output signal ue, determined at the start of the sensor's working life.
  • the output signal of the comparator 18 is then the signal S, with which the signal processor 12 (if necessary) registers a failure.
  • the alternating component uw is decoupled from the test voltage UL, and rectified.
  • the threshold value ud is derived from the output signal ue of sensor 2 when it first begins operating. Subsequent measurements of the output signal are determined and compared with ud. When the output signal ue reaches the threshold value ud, the signal S changes, and informs an operator of the failure of sensor 2.
  • the direct component ug and the alternating component uw of the output signal of the amplifier 14 are fed to a low pass filter. Further, the multiplier 20 is activated by the output signal ue of the low pass filter 17. The multiplier 20 produces a signal Y from both the direct component ug and the output signal ue, that corresponds to the corrected concentration value x of the gas activated in sensor 2. An operator can read off the concentration of the measured gas from signal Y.
  • signal Y represents an output signal which is corrected with respect to the electrochemically active area of sensor 2. This means that a change of the active area is taken into account by signal Y, and therefore cannot lead to a falsification of signal Y.
  • the quoted correction takes place automatically and permanently by means of the signal ue, so that a so-called online correction is present.
  • Signal Y not only gives a user information on the concentration of the gas activated in sensor 2, but also monitors continuously possible ageing phenomena or the like of sensor 2, and automatically corrects them.
  • ground potential (or like terms such as “ground voltage” or “earth” potential or voltage) is used conveniently in this specification to denote a reference potential.
  • reference potential may typically be zero potential, it is not essential that it is so, and may be a reference potential other than zero.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Molecular Biology (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Investigating Or Analyzing Materials By The Use Of Electric Means (AREA)
PCT/GB1998/002967 1997-10-06 1998-10-06 Electrochemical sensors WO1999018430A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU93564/98A AU9356498A (en) 1997-10-06 1998-10-06 Electrochemical sensors

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19743979.9 1997-10-06
DE1997143979 DE19743979A1 (de) 1997-10-06 1997-10-06 Verfahren zum Betreiben eines elektrochemischen Sensors sowie elektrische Schaltung für einen elektrochemischen Sensor

Publications (1)

Publication Number Publication Date
WO1999018430A1 true WO1999018430A1 (en) 1999-04-15

Family

ID=7844659

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/GB1998/002967 WO1999018430A1 (en) 1997-10-06 1998-10-06 Electrochemical sensors

Country Status (3)

Country Link
AU (1) AU9356498A (de)
DE (1) DE19743979A1 (de)
WO (1) WO1999018430A1 (de)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6830730B2 (en) 2001-09-11 2004-12-14 Spectrolanalytical Instruments Method and apparatus for the on-stream analysis of total sulfur and/or nitrogen in petroleum products
WO2008098261A2 (en) * 2006-12-29 2008-08-14 Medtronic Minimed, Inc. Method and system for detecting the age, hydration, and functional states of sensors using electrochemical impedance spectroscopy
US20080289959A1 (en) * 2007-05-25 2008-11-27 West Steven J Self-diagnostic sensor system
WO2009026236A1 (en) * 2007-08-21 2009-02-26 Medtronic Minimed, Inc. Method and system for remedying sensor malfunctions detected by electrochemical impedance spectroscopy
CN100514052C (zh) * 2006-05-26 2009-07-15 中国科学院电子学研究所 快速稳定的互补金属氧化物半导体恒电位仪电路
US7638033B2 (en) 2003-04-08 2009-12-29 Roche Diagnostics Operations, Inc. Biosensor system
US8114269B2 (en) 2005-12-30 2012-02-14 Medtronic Minimed, Inc. System and method for determining the point of hydration and proper time to apply potential to a glucose sensor
US8168060B2 (en) * 2007-06-04 2012-05-01 Ford Global Technologies, Llc System and method for improving accuracy of a gas sensor
WO2019027701A1 (en) 2017-08-03 2019-02-07 Industrial Scientific Corporation SYSTEMS AND METHODS FOR ASSESSING TOXIC GAS SENSORS EMPLOYING ELECTROCHEMICAL IMPEDANCE SPECTROSCOPY
CN115666372A (zh) * 2020-06-16 2023-01-31 德尔格安全股份两合公司 电化学传感器装置、呼吸酒精测量设备和用于确定电化学传感器的电极活力的方法

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102005032134A1 (de) * 2005-07-07 2007-01-18 Endress + Hauser Wetzer Gmbh + Co Kg Messvorrichtung zur Bestimmung und/oder Überwachung einer Prozessgröße und Verfahren zur Überwachung der Messvorrichtung

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3661748A (en) * 1970-04-07 1972-05-09 Instrumentation Labor Inc Fault sensing instrumentation
DE3239572A1 (de) * 1981-11-11 1983-05-26 Horiba Ltd., Kyoto Vorrichtung zur messung von ionenkonzentrationen
CH636447A5 (en) * 1977-08-26 1983-05-31 Ciba Geigy Ag Device for monitoring electrodes
WO1990012315A1 (en) * 1989-04-04 1990-10-18 Neotronics Limited Fault detection in electrochemical gas sensing equipment
EP0497994A1 (de) * 1991-01-28 1992-08-12 KNICK ELEKTRONISCHE MESSGERÄTE GMBH & CO. Verfahren und Schaltungsanordnung zur Überwachung von ionen- oder redoxpotential-sensitiven Messketten
WO1993008477A1 (en) * 1991-10-25 1993-04-29 Rosemount Analytical Inc. SELF DIAGNOSTIC pH SENSOR
DE4318891A1 (de) * 1993-06-07 1994-12-08 Mannesmann Ag Elektrochemisches Gasspurenmeßsystem mit Funktionskontrolle

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3661748A (en) * 1970-04-07 1972-05-09 Instrumentation Labor Inc Fault sensing instrumentation
CH636447A5 (en) * 1977-08-26 1983-05-31 Ciba Geigy Ag Device for monitoring electrodes
DE3239572A1 (de) * 1981-11-11 1983-05-26 Horiba Ltd., Kyoto Vorrichtung zur messung von ionenkonzentrationen
WO1990012315A1 (en) * 1989-04-04 1990-10-18 Neotronics Limited Fault detection in electrochemical gas sensing equipment
EP0497994A1 (de) * 1991-01-28 1992-08-12 KNICK ELEKTRONISCHE MESSGERÄTE GMBH & CO. Verfahren und Schaltungsanordnung zur Überwachung von ionen- oder redoxpotential-sensitiven Messketten
WO1993008477A1 (en) * 1991-10-25 1993-04-29 Rosemount Analytical Inc. SELF DIAGNOSTIC pH SENSOR
DE4318891A1 (de) * 1993-06-07 1994-12-08 Mannesmann Ag Elektrochemisches Gasspurenmeßsystem mit Funktionskontrolle

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
L. MAKADMINI: "SELF-CALIBRATING ELECTROCHEMICAL SENSOR", 1997 INTERNATIONAL CONFERENCE ON SOLID-STATE SENSORS AND ACTUATORS, vol. 1, April 1997 (1997-04-01), CHICAGO, US, pages 299 - 302, XP002091408 *

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6867047B2 (en) 2001-09-11 2005-03-15 Spectro Analytical Instruments Method and apparatus for preventing nitrogen interference in pyro-electrochemical methods
US6830730B2 (en) 2001-09-11 2004-12-14 Spectrolanalytical Instruments Method and apparatus for the on-stream analysis of total sulfur and/or nitrogen in petroleum products
US7638033B2 (en) 2003-04-08 2009-12-29 Roche Diagnostics Operations, Inc. Biosensor system
US8114269B2 (en) 2005-12-30 2012-02-14 Medtronic Minimed, Inc. System and method for determining the point of hydration and proper time to apply potential to a glucose sensor
US8114268B2 (en) 2005-12-30 2012-02-14 Medtronic Minimed, Inc. Method and system for remedying sensor malfunctions detected by electrochemical impedance spectroscopy
US7985330B2 (en) 2005-12-30 2011-07-26 Medtronic Minimed, Inc. Method and system for detecting age, hydration, and functional states of sensors using electrochemical impedance spectroscopy
US8608924B2 (en) 2005-12-30 2013-12-17 Medtronic Minimed, Inc. System and method for determining the point of hydration and proper time to apply potential to a glucose sensor
CN100514052C (zh) * 2006-05-26 2009-07-15 中国科学院电子学研究所 快速稳定的互补金属氧化物半导体恒电位仪电路
WO2008098261A3 (en) * 2006-12-29 2008-11-06 Medtronic Minimed Inc Method and system for detecting the age, hydration, and functional states of sensors using electrochemical impedance spectroscopy
WO2008098261A2 (en) * 2006-12-29 2008-08-14 Medtronic Minimed, Inc. Method and system for detecting the age, hydration, and functional states of sensors using electrochemical impedance spectroscopy
US8603307B2 (en) * 2007-05-25 2013-12-10 Thermo Fisher Scientific, Inc. Self-diagnostic sensor system
US20080289959A1 (en) * 2007-05-25 2008-11-27 West Steven J Self-diagnostic sensor system
US8168060B2 (en) * 2007-06-04 2012-05-01 Ford Global Technologies, Llc System and method for improving accuracy of a gas sensor
WO2009026236A1 (en) * 2007-08-21 2009-02-26 Medtronic Minimed, Inc. Method and system for remedying sensor malfunctions detected by electrochemical impedance spectroscopy
JP2010537198A (ja) * 2007-08-21 2010-12-02 メドトロニック ミニメド インコーポレイテッド 電気化学インピーダンス分光法によって検出されるセンサ誤動作に対処するための方法およびシステム
WO2019027701A1 (en) 2017-08-03 2019-02-07 Industrial Scientific Corporation SYSTEMS AND METHODS FOR ASSESSING TOXIC GAS SENSORS EMPLOYING ELECTROCHEMICAL IMPEDANCE SPECTROSCOPY
CN110573869A (zh) * 2017-08-03 2019-12-13 工业科技有限公司 用于使用电化学阻抗谱来评估有毒气体传感器的系统和方法
EP3662275A4 (de) * 2017-08-03 2021-05-05 Industrial Scientific Corporation Systeme und verfahren zur bewertung von toxischen gassensoren unter verwendung elektrochemischer impedanzspektroskopie
US11079363B2 (en) 2017-08-03 2021-08-03 Industrial Scientific Corporation Systems and methods for evaluating toxic gas sensors using electrochemical impedance spectroscopy
CN110573869B (zh) * 2017-08-03 2023-02-21 工业科技有限公司 用于使用电化学阻抗谱来评估有毒气体传感器的系统和方法
CN115666372A (zh) * 2020-06-16 2023-01-31 德尔格安全股份两合公司 电化学传感器装置、呼吸酒精测量设备和用于确定电化学传感器的电极活力的方法

Also Published As

Publication number Publication date
DE19743979A1 (de) 1999-04-08
AU9356498A (en) 1999-04-27

Similar Documents

Publication Publication Date Title
EP0467902B1 (de) Fehlerdetektion in elektrochemischen gassensorvorrichtungen
EP0800787B1 (de) Vorrichtung zur Überwachung von Messelektroden zum Erfassen von physiologischen Signalen
US5611909A (en) Method for detecting source of error in an amperometric measuring cell
EP0315854B1 (de) Verfahren und Vorrichtung zur Messung der Hautfeuchtigkeit
WO1999018430A1 (en) Electrochemical sensors
JPH08507368A (ja) 電気化学的電池の充電状態を決定する方法および装置
JPS62242849A (ja) 電極測定システムにおける電極の性能を試験する装置
JP2005221487A (ja) 二次電池の内部インピーダンス測定方法、二次電池の内部インピーダンス測定装置、二次電池劣化判定装置及び電源システム
EP0798557A2 (de) Gassensor und Verfahren zum Messen der Menge von spezifischen Verbindungen in einem Nachweisgas
JP3158063B2 (ja) 非接触電圧計測方法及び装置
EP0645623B1 (de) Verfahren zur Überwachung des Säuregehaltes in Plattierungsbädern
US20050212534A1 (en) Method and apparatus for monitoring corrosion
US20230015110A1 (en) Method for Diagnosing at Least One Fuel Cell Stack of a Fuel Cell Device, Computer-Readable Storage Medium, and Fuel Cell Diagnostic System
JPH09184866A (ja) ケーブルの活線下劣化診断方法
US11320398B2 (en) Sensor arrangement for voltammetry
CN104215667A (zh) 具有时分多路复用相位检测的手持式测试仪
EP3422025B1 (de) Verfahren und vorrichtung zur frequenzanpassung
JPH07128387A (ja) 非接地配線方式の電路の絶縁監視装置
JP2001083183A (ja) 電流検出回路及びその検査方法
RU2201477C1 (ru) Способ контроля сопротивления изоляции между электролизером и землёй и устройство для его осуществления
JP2000147038A (ja) コンデンサ用測定装置
AU644355B2 (en) Fault detection in electrochemical gas sensing equipment
US7046016B2 (en) Potential fixing device, potential fixing method, and capacitance measuring instrument
JP2547796B2 (ja) ケーブル活線劣化診断装置
JP2968763B2 (ja) 液体現像剤の濃度検出,管理方法

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AL AM AT AU AZ BA BB BG BR BY CA CH CN CU CZ DE DK EE ES FI GB GD GE GH GM HR HU ID IL IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MD MG MK MN MW MX NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT UA UG US UZ VN YU ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW SD SZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
NENP Non-entry into the national phase

Ref country code: KR

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

122 Ep: pct application non-entry in european phase
NENP Non-entry into the national phase

Ref country code: CA