CA2106666A1

CA2106666A1 - Electrode calibration

Info

Publication number: CA2106666A1
Application number: CA 2106666
Authority: CA
Inventors: Stephen John Edwards; Graham Anthony Fuggle
Original assignee: Individual
Current assignee: Eastman Kodak Co
Priority date: 1991-04-04
Filing date: 1992-04-02
Publication date: 1992-10-05
Also published as: WO1992017775A1; JPH06506060A; AU1430692A; GB9107036D0; EP0579632A1; BR9205841A

Abstract

An electro-analytical sensing instrument such as a pH meter has a sensing electrode which is placed in an electrolyte and voltages are read out in order to measure the properties of the electrolyte such as pH. The present invention enables an electrode assembly to be calibrated at one site and used at other sites and with other instruments without the need for re-calibration. This is achieved by providing a calibration unit including a memory which is kept as part of the electrode assembly for use at other sites.
Various electrode assemblies to which the invention can be applied are described.

Description

WO 92/17775 ~ fi 6~ ~ Pcr/EP92/oo769 ELEC~RODE CALIBRATION

This invention relates to electro-analytical sensing instruments having sensor probe electrodes, and is particularly concerned with the calibration and use of the electrodes.

When measuring an active electrochemical species potentiometrically, that is by measurement of the voltage between electrodes in an elec$rolyte (the analyte), it is first essential to calibrate the instrument in standard solutions or buffers of known activity to allow the slope and offset voltage to be determined and used in subsequent measurements. These values are either held by analogue potentiometers in the measurement instrument circuits, or stored in memory, if the instrument is digital. Once calibrated, the measuring electrodes - either a separable indicator electrode and reference electrode, or a combined pair - cannot be disconnected from that instrument and connected to another, perhaps in a different area, without re-calibration.

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,' ,~ , , WO 92/1777~ 2 1~ 6 ~ & ~ PCT/EP92/00769 The present invention is concerned therefore with the proble~ of allowing the calibration and measurement of such sensors to be carried out at one site or in one instrument and used in another instrument or at another site. -.

The invention is further concerned with the problem -~
of providing a device which can b2 used for any typ2 : . .
of sensor which requires r~-c21ibration.
' ' ' ' ' ''' It is known that the volLage m~asur~d ~h~n usins a potentiometric electrochemical sensor is mainly .-~
dependant on the analyte, and is given by the . .
following Nernst equation: - ;
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E(measured) E(indicator electrode half cell) Eref where E(~n~c~ )electrode = E(stan~a~ ) species) and Eref E(reference half cell) E(junction potentials) Aspeciesis the activity of species A and is approximately equal to the concentration of A in dilute solutions, ,~

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In normal circumstances the reference half cell and junction potentials are not predictable to more than a few millivolts and may vary considerably hetween different reference electrodes. If it iis i -S necessary to obtain a direct instrument read out in either concentration or In(concentration) it is necessary to first convert from the millivolts measured by calibrating the system on a number of standard solutions. The difference between theoretical millivolts and those measured is the offset voltage of that particular system. It is stored in the measuring instrument for later use, either by using a potentiometer to offset the millivolts measured back to the theoretical reading or digitally by using a micro-processor and memory.

In a perfect system the millivolts measured are proportional to the logarithm of the activity of the analyte. From the Nernst equation this can be seen to be:
(RT/nF)- In(Aspecies) or 2.303 . (RTlnF) log(Aspecies) At a temperature of 25C this is 59.13mV per r decade increase in concentration.

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In practice this theoretical factor is rarely obkained and an empiral factor calculated from the calibration data obtained ~y ~easurin~ standard solutions is used instead. This factor is obtained -and stored for later use in an analogue instrument by setting the gain of the input circuits when meas~ring the standard solutions. In a micro-processor instrument this is stored directly as a factor in memory. This factor is defined as the slope of the ~ ;
system and may be presented as a percentage.

As stated above when measuring an active electrochemical species potentiometrically, it is first essential to calibrate in standard solutions or buffers of known activity to allow the slope and -offset voltage to be determined and used in subsequent measurements. `

EP-A-0,074,498 discloses a system in which a calibration unit includes a memory which includes calibration data, however calibration involves processing at a remote site and therefore there is a risk of inaccuracies arising.

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According to the invention the calibration data is stored in a calibration unit in close physical assoc ation with the electrode or electrcde pair assembly rather than in the broader confines of the 5 instrument itself and the unit includes it Gwn ~ -.
microprocessor where calibration can take place in situ. This means that the electrode assembly and calibration unit can ~e disconnected from the instrument and taken to a remote site. A new instrument can then read and process this information and be ready to measure without the need for re-calibration and without the need to feed the data to a remote site along circuitry of unkncwn parameters. . .
Accordingly the invention provides a measurinq instrument for connection in a sensing instrument which measuring instrument has measuring sensors which require calibration, and located in close association with said sensors a calibration unit including a memory means which is arranged to store calibration data to enable the assembly to be used with more than one sensing instrument, characterised in that the calibration unit further comprises a microprocessor which enables the sensors to be calibrated in situ.

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This approach means that one indicator and reference electrode pair can be calibrated in a ~. ~
laboratory or clean area and can then be taken into a ~ .
factory environment, where buffer or standard solution -~
S might be contaminated, for solution measurements.

~ ' Preferably the assembly in accordance with the :
invention comprises a small memory and communications ~. -integrated circuit sealed into either electrode or `
probe or holder assembly together with a micro-processor instrument. The electrode pair can be -calibrated in the normal process with buffers or standard solutions and the calibration data such as the slope and the offset voltage, can then be stored ',.-.,: .

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WO 92/1777~ ~ 1 0 fi ~ 6 i~ PCT/EP92/00769 in the memory means in the electrode pair via a serial communications link. This information may then be stored in non-volatile memory, for example in battery-backed RAM, EPROM or EEPROM for future use. The electrodes may then be disconnected, taken into a new -area and connected to a different instrument. The new lnstrument will then retrieve this calibration data and be ready to carry out measurements.

Other information regarding time of calibration, safe time available before re-calibration is necessary, identification numbers and electrode typ2 can also be stored.

The memory means is conveniently incorporated in the lead assembly of an existing electrode system. ;

The memory means may also include line drivers or impedance converters if the electrodes are of high impedance or the measuring instrument is likely to be located at a large distance from the electrodes.

The electrode assembly according to the invention may also be made intrinsically safe for areas where inflammable solvents are used. Calibration can then - take place in a normal area where water baths and ~ .
.

7~ PCT/EP92/0~769 _ 7 _ 21~
associated equipment can be safely used. Connection ~ :
of the assembly to the measurement instrument is then preferably made via a shunt-diode safety barrier, ~ :

S Several embodLments of the invention will now be described by way of example with reference to the -::.
accompanying drawings in which:

Figure 1 is a schematic diagram of an indicator electrode with the calibration unit installed;

Figure 2 is a schematic diagram of an electrode .:
combination pair with the ca~ibration unit installed;
` .: - .
Figure 3 is a schematic diagram of a sensor probe with the calibration unit installed in a corner unit -separate from the sensors;
:
Fi~ure 4 shows a schematic diagram of an electxode :::
system with the calibration unit installed in a lead; .; .

Fiqure S is a block circuit diaqram of the ~.s:~-calibration unit; and :: '~.:. `' -, .;

WO 92/1777~ PCT/EP92/00769 6~ 8 -Figures 6a to 6e show various known electrodes which can incorporate the invention.

Figure 1 shows an indicator electrode incorporating a calibration unit. A cylindrical glass container 1 carries at its lower end an electrode membrane 2 and encloses an electrolyte 3. The membrane 2 is connected by an electrically conducting lead 4 to a screened multi strand output lead 5. The lead 4 is screened by a metallic screening sheath 6. This is shown schematically but in practice can be located between inner and outer glass concentric walls rather than within the electrolyte 3.

The glass container 1 is carried by a carrier 7 at the top of the electrode assembly which as well as supporting the container 1 encloses wiring which feeds out into the multicore cable 5. The carrier 7 also encloses a calibration unit 8 whose output leads are connected into the multi strand cable 5.

The electrode is used in conjunction with a reference electrode, which then forms a part of the calibrated pair. The significant difference in the reference electrode is that instead of an electrode membrane 2 across which a voltage will be developed, a porous wo 92/~777~ PCT/EP92/00769 - - ?~ ~ ~ 6 ~
wall i9 employed at its lower end so that the reference electrode is retained at a potential derived from the solution within the electrode and is therefore constant. While the calibration data is -retained in the unit associated with the indicator electrode, the calibration also takes account of variations within the reference electrode. Therefore a particular reference electrode always has to be identlfied and used together with the same calibrated indicator electrode.

Figure 2 shows a combined electrode consis~ing essentially of a measuring electrode of the kind sho~n in Figure 1 combined with a reference electrode surrounding it.

The same reference numbers are used for the same component features as in Figure 1 example and these components are essentially the same. However surrounding the measuring electrode is an enclosing glass jacket lO thus defining within an annular compartment a reservoir for a reference solution 11.
Within the reference solution ll is a reference element 12, and the lower face of the circular jacket 10 is closed by a porous annular plug 13. Thus, the ~, ~ ' .;
, ~, .

WO 92/l777~ PCT/EP92/00769 6;.) - lo-reference element can be maintained at a constant potential determined by the reference solution.

This contrasts with the measuring electrode where a glass membrane 2 allows a potential to develop across that membrane in order to sense the difference in value between the liquids on either side of the sensing element 2 (for measurement of Ph etc). The reference element 12 is then connected via a conducting line 14 into the multi strand output cable 5.

Figure 3 shows a further arrangement. In this arrangement, a measuring electrode 20 and a reference electrode 21 (substantially of the form shown in Figure 1) are carried out in a connecting carrier 22 ;
which connects to the main carrier 7. The two electrodes 20 and 21 and an earthing terminal 22 are connected by conductors 23 via plugs and sockets 24 to an output amplifier 25 and thence to the multi s~rand cable 5 for feeding to the instrument (nat shown).

Figure 4 shows a further form of the invention where a combined electrode 31 is fed by conductors 32 via the calibration unit 8 to the instrument (not wo 92/1777~ PCT/EP92/00769 11- 2~ o shown), i.e the calibration unit is incorporated in the electrode connecting lead.

In each of these described examples, the calibration unit 8 is always associated with one or both electrodes whereby when the or each electrode is unplugged from the instrument and taken to another location, it will always have its correct calibration.
', ' Figure 5 sho~s a schematlc of a partlcular form of calibration unit. This com~rises a pair of high Lmpedance operational amplifiers 41 and 42 which are fed from the sensors via input leads at the right - hand side of the Figure and thence are fed to a pair of output leads on the left hand side of Figure 5.
The unit also incorporates a microprocessor with encapsulated battery and memory unit 43 fed from multi-strand cable S via serial line drives 44 and 45.
,.
Thus in practice a pair of electrodes can be calibrated and the calibration stored in the memory unit 43 and the electrodes will then be available for use when plugged into other inslruments at other , , sites.

The invention can be applied to various forms of ,'' ' :' ' ." ' . ~

WO 92/l777~ PCT/EP92/00769 ~ 2 -known measuring electrode, A unit of the kind shown in Figure 5 for example can readily be incorporated in the output lead or in the carrier head for the , electrode.

Thus, Figure 6a to Figure 6e show various electrodes to which the invention may be applied.
These electrodes are as follows ~

Fisure 6a shows a metal electrode, Fioure 6b shows a coated metal electrode, Fi~re 6c shows a solid s~ate ion selective electrode, Figure 6d shows a liquid iron exchange ion selective electrode, Figure 6e is a pH electrode.

In these electrodes the components are as follows:-In Figures 6a and 6b, 51 denotes the insulation and 52 is the electrode proper while in Figure 6b 53 denotes a sensing coating.

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In regard to Figure 6c~ the solid state ion :`
selectlve electrode, 55 denotes an electrically conductive contact for a solid membrane 54.
.' '.

In Figure 6d, the liquid ion exchange ion ~ . -.
selective electrode 57 is an internal reference solution 58 is an internal reference .;
element and 56 is a sensing membrane across which a volta~e can be developed.

Finally, Figure 6e den3tes a conventional pH
electrode incorporating 2 glass membrane 59 and ;.;
extending from a glass bcdy 60 which encloses an :-internal reference element 61 within an internal reference solution 62.

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Claims

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1. A measuring instrument for connection in a sensing instrument which measuring instrument has measuring sensors which require calibration, and located in close association with said sensors a calibration unit (8) including a memory means (43) which is arranged to store calibration data to enable the assembly to be used with more than one sensing instrument, characterised in that the calibration unit further comprises a microprocessor which enables the sensors to be calibrated in situ.

2. An instrument according to claim 1 in which the sensors are measuring electrodes of an electro-analytical sensing instrument.

3. An instrument according to claim 2 in which the measuring electrodes are Ph electrodes.

4. An instrument according to any of the preceding claims in which the sensor includes a carrier housing (7) and the calibration unit (8) is located within said carrier housing.

5. An instrument according to any of the preceding claims comprising a pair of electrodes one of which is an indicator electrode and the other is a reference electrode and said calibration unit is associated with the indicator electrode.

6. An instrument according to claim 5 in which the indicator electrode and reference electrode are combined in a single unit.

7. An instrument according to claim 1 in which the calibration unit is carried within an output lead of the sensor.

8. An electrode assembly for use in an instrument according to any one of the preceding claims.