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Pure&App/. Chern., Vol. 63, No. 9, pp. 1247-1250, 1991.
Printed in Great Britain.
@ 1991 IUPAC
ADONIS 206922209100118Y
INTERNATIONAL UNION OF PURE
AND APPLIED CHEMISTRY
ANALYTICAL CHEMISTRY DIVISION
COMMISSION ON GENERAL ASPECTS OF ANALYTICALCHEMISTRY"?
CHEMICAL SENSORS
DEFINITIONS AND CLASSIFICATION
Prepared for publication by
ADAM HULANICKI', STANISEAW GEAB and FOLKE INGMAN2
'Department of Chemistry, University of Warsaw, Warsaw, Poland
*Department of Analytical Chemistry, Royal Institute of Technology, Stockholm, Sweden
*Membership ofthe Commissionduring the preparation of the report (1985-90) was as follows:
1985-87
Chairman: G. Ackermann (GDR); Secretary: D. Thorburn Burns (UK); Titular Members: St.
Glab (Poland); F. Ingman (Sweden); D. L. Massart (Belgium); S. B. Sawin (USSR); L.
Sommer (Czechoslovakia); Associate Members: D. Baylocq (France); A. Hulanicki (Poland);
J. Incztdy (Hungary); W. E. van der Linden (Netherlands); M. Takagi (Japan); P. C. Uden
(USA); G. Vigh (USA); E. V. Wanninen (Finland); B. D. Westerlund (Sweden); National
Representatives:J. F. Desreux (Belgium); 0.Budevsky (Bulgaria); J. Garaj (Czechoslovakia).
1987-89
Chairman: D. Thorburn Burns (UK); Secretary: F. Ingman (Sweden); Titular Members: St.
Glab (Poland); D. L. Massart (Belgium); L. Sommer (Czechoslovakia); P. C. Uden (USA);
W. E. van der Linden (Netherlands); Associate Members: D. Baylocq (France); A. Marton
(Hungary); H. Muller (GDR); S. B. Sawin (USSR); M. Takagi (Japan); G. Vigh (USA);
E. V. Wanninen (Finland); B. D. Westerlund (Sweden); P. J. Worsfold (UK); National
Representatives: J. F. Desreux (Belgium); 0. B. Budevsky (Bulgaria); J. Garaj (Czecho-
slovakia);G. Ackermann (GDR);J. Incztdy (Hungary);A. Hulanicki (Poland);S. Ates (Turkey).
1989-91
Chairman: F. Ingman (Sweden); Vice-chairman: R. E. Van Grieken (Belgium); Secretary:
W. E. van der Linden (Netherlands); Co-Secretary: C. L. Graham (UK); Titular Members:
L. A. Currie (USA); St. Glab (Poland); W. Horwitz (USA); D. L. Massart (Belgium); M.
Parkany (Switzerland); Associate Members: P. S. Goel (India); Y. Gohshi (Japan); H. Muller
(GDR); M. Otto (GDR); G. J. Patriarche (Belgium); S. B. Savvin (USSR); J. W. Stahl
(USA); P. J. Worsfold (UK); National Representatives: Tania M. Tavares (Brazil); L. Sommer
(Czechoslovakia); D. Klockow (FRG); K. Danzer (GDR); J. InczBdy (Hungary); D.
Thorburn Burns (UK); R. D. Reeves (New Zealand); A. Hulanicki (Poland); B. Schreiber
(Switzerland); S . Ates (Turkey); G. Svehla (UK).
tCommission title 1985-89: Commission on AnalyticalReactions, Reagents, and Separations
Republication of this report is permitted without the need for formal IUPAC permission on condition that an
acknowledgement, with full reference together with IUPAC copyright symbol (01991 IUPAC), is printed.
Publication of a translation into another language is subject to the additional condition of prior approval from the
relevant IUPAC National Adhering Organization.
Chemical sensors: definitions and classification
DEFINITIONS
A chemicalsensoris a device that transformschemicalinformation,ranging from the concentration of a
specific sample component to total composition analysis, into an analytically useful signal. The
chemical information,mentioned above,may originatefrom a chemicalreaction of the analyte or from a
physical property of the system investigated.
A physical sensor is a device that provides information about a physicalproperty of the system.
A chemical sensoris an essential componentof an analyzer. In additionto the sensor,the analyzermay
contain devicesthat perform the followingfunctions:sampling,sampletransport, signalprocessing, data
processing. An analyzer may be an essential part of an automated system. The analyzer working
according to a sampling plan as a functionof time acts as a monitor.
Chemical sensorscontain two basic functionalunits: a receptor part and a transducerpart. Some sensors
may includea separator which is, for example,a membrane.
In the recepror part of a sensor the chemical information is transformed into a form of energy which
may be measured by the transducer.
The transducer part is a device capable of transforming the energy carrying the chemical information
about the sample into a useful analyticalsignal.The transduceras suchdoes not show selectivity.
Thereceptorpart of chemicalsensorsmay be based upon variousprinciples:
- physical, where no chemical reaction takes place. Qpical examples are those based upon
measurementof absorbance,refractiveindex,conductivity,temperatureor mass change.
- chemical, in which a chemical reaction with participation of the analyte gives rise to the
analytical signal.
- biochemical, in which a biochemical process is the source of the analytical signal. Qpical
examples are microbial potentiometric sensors or immunosensors. They may be regarded as a
subgroupof the chemical ones. Such sensorsare called biosensors.
In some cases it is not possible to decide unequivocally whether a sensor operates on a chemicalor on a
physical principle. This is, for example,the case when the signalis due to an adsorption process.
Sensors are normally designed to operate under well defined conditions for specified analytes in certain
sample types. Therefore, it is not always necessary that a sensor responds specifically to a certain
analyte.Under carefully controlled operatingconditions,the analyte signal may be independentof other
sample components, thus allowing the determination of the analyte without any major preliminary
treatment of the sample. Otherwiseunspecificbut satisfactory reproducible sensors can be used in series
for multicomponent analysis using a multivariate calibration software and signal processing. Such
systemsfor multicomponentanalysis arecalled sensorarrays.
CLASSIFICATION OF SENSORS
The developmentof instrumentation,microelectronicsand computersmakes it possibleto design sensors
utilizing most of the known chemical, physical and biological principles that have been used in
chemistry.
Chemicalsensorsmay be classifiedaccordingto the operatingprinciple of the transducer.
1.Oprical devicestransform changes of optical phenomena,which are the result of an interactionof the
analyte with the receptor part. This group may be further subdivided according to the type of optical
propertieswhich have been applied in chemicalsensors:
a) absorbance,measured in a transparentmedium,causedby the absorptivity of the analyte itself or by a
reaction with some suitableindicator.
b) reflectanceis measured in non-transparentmedia, usually using an immobilizedindicator.
c) luminescence,based on the measurementof the intensityof lightemitted by a chemicalreaction in the
receptorsystem.
1248
Chemical sensors: definitions and classification 1249
d) fluorescence, measured as the positive emission effect caused by irradiation. Also, selective
quenching of fluorescencemay be the basis of suchdevices.
e) refractive index, measured as the result of a change in solution composition. This may include also a
surfaceplasmon resonanceeffect.
f ) optothermaleffect, based on a measurementof the thermal effectcaused by light absorption.
g) light scattering,based on effectscausedby particlesof definite sizepresent in the sample.
The application of many of these phenomena in sensors became possible because of the use of optical
fibres in various configurations. Such devices have also been called optodes. It should be emphasized
that fibre optics now commonly used are only technical devices applicable in a large group of optical
sensorswhich can be based on variousprinciples.
2. Electrochemical devices transform the effect of the electrochemical interaction analyte -electrode
into a useful signal. Such effects may be stimulated electrically or may result in a spontaneous inter-
actionat the zero-currentcondition.The followingsubgroupsmay be distinguished:
a) voltammetricsensors, including amperometricdevices, in which currentis measured in the d.c. or a.c.
mode. This subgroup may include sensors based on chemically inert electrodes, chemically active
electrodes and modified electrodes. In this group are included sensors with and without (galvanic
sensors)externalcurrent source.
b) potentiometricsensors,in which the potential of the indicatorelectrode (ion-selectiveelectrode,redox
electrode,metaVmeta1oxideelectrode)is measured againsta referenceelectrode.
c) chemically sensitized field effect transistor (CHEMFET)in which the effect of the interaction
between the analyte and the active coating is transformed into a change of the source-drain current.The
interactionsbetween the analyte and the coating are, from the chemical point of view, similar to those
foundin potentiometric ion-selectivesensors.
d) potentiometric solid electrolyte gas sensors, differing from class 2b) because they work in high
temperaturesolidelectrolytesand are usually appliedfor gas sensingmeasurements.
3. Electrical devices based on measurements, where no electrochemical processes take place, but the
signalarisesfrom the changeof electricalpropertiescausedby the interactionof the analyte.
a) metal oxide semiconductorsensors used principally as gas phase detectors,based on reversibleredox
processesof analytegas components.
b) organic semiconductor sensors, based on the formation of charge transfer complexes, which modify
the chargecarrierdensity.
c) electrolyticconductivity sensors.
d) electricpermittivity sensors.
4. Mass sensitive devices transform the mass change at a specially modified surface into a change of a
property of the supportmaterial. Themass changeis causedby accumulationof the analyte.
a) piezoelectric devices used mainly in gaseous phase, but also in solutions, are based on the
measurementthe frequency change of the quartz oscillator plate caused by adsorption of a mass of the
analyteat the oscillator.
b) surface acoustic wave devices depend on the modification of the propagation velocity of a generated
acousticalwave affected by the depositionof a definitemass of the analyte.
5. Magnetic devices based on the change of paramagnetic properties of a gas being analysed.These are
representedby certain types of oxygen monitors.
6. Thermometricdevices based on the measurement of the heat effects of a specific chemicalreaction or
adsorption which involve the analyte. In this group the heat effects may be measured in various ways,
for examplein the so called catalytic sensorsthe heat of a combustionreaction or an enzymaticreaction
is measured by use of a thermistor. The devices based on measuring optothermal effects (If) can
alternativelybe included in this group.
1250 COMMISSION ON GENERALASPECTS OF ANALYTICAL CHEMISTRY
7. Other physical properties as for example X-, p- or r- radiation may form the basis for a chemical
sensorin casethey areused for determination of chemical compostion.
This classification represents one of the possible alternatives. Sensors have, for example, been classified
not according to the primary effect but to the method used for measuring the effect. As an example can
be given the so-called catalytic devices in which the heat effect evolved in the primary process is
measured by the change in the conductivity of a thermistor. Also, the electrical devices are often put into
onecategory together with the electrochemical devices.
Sensors have also been classified according to the application to detect or determine a given analyte.
Examples are sensors for pH, for metal ions or for determing oxygen or other gases.
Another basis for the classification of chemical sensors may be according to the mode of application, for
example sensorsintended for use in vivo, or sensorsfor process monitoring and so on.
It is, of course, possible to use various cassifications as long as they are based on clearly defined and
logically arranged principles.
The biosensors are not presented as a special class because the process on which they are based is, in
general, common to chemical sensors. They may be also differentiated according to the biological
elements used in the receptor. Those may be: organisms, tissues, cells, organelles, membranes,
enzymes, antibodies, etc. The biosensors may have several enzymatic systems coupled which serve for
amplificationof the signal.
Various sensorsmay be combined in sets which are often called multisensors.
GENERAL REFERENCES
1. Proceedings of the International Meeting on Chemical Sensors, Fukuoka, Japan, September 19-22, 1983,
Editors: T. Seyma, K. Fueki,J. Shiokawa and S. Suzuki, Elsevier-Kodanscha, Amsterdam and Tokyo,
1983.
H. Wohltjen, Chemical Microsensorsand Microinstrumentation,Anal. Chem.,%,87A, 1984.
W.R. Seitz, Chemical SensorsBased on Immobilized Indicators and Fibre Optics, CRC CriticalReviews
in Anal. Chem., 19,135, 1988.
M. Thompson and U. J. Krull, Biosensors and Bioprobes, Trends in Anal. Chem.,3, 173, 1984.
T.E. Edmonds (ed.),Chemical Sensors,Blackie and Sons Ltd., London, 1988.
A.P.F. Turner, I. Karube and G.S. Wilson (eds.), Biosensors. Fundamentals and Applications,Oxford
UniversityPress,New York, 1987.
R. Niessner, Chemische Sensoren:Principienund Anwendungen in Analytiker Taschenbuch,vol. 7. (eds.:
W. Fresenius et. al.) SpringerVerlag,Berlin, 1988,p. 55.
D. Schuetzle, R. Hammerle and J. Butler (eds.), Fundamentals and Applications of Chemical Sensors,
ACS Symposium Series, 309 AmericanChemical Society, 1986.
2.
3.
4.
5.
6.
7.
8.
9. W. Gopel, Entwicklung Chemischer Sensoren. Empirische Kunst oder systematische Forschung? Techn.
Messen,2,47,92, 175,1985.
10.
11.
12.
13.
14.
C. Nylander,Chemical Sensorsand Biological Sensors,J. Phys. Sci. Instr., Is,736, 1985.
J. Janata and A. Bezegh,Chemicalsensors,Anal.Chem.,@, 62R, 1988.
J. Janata, R.J. Huber (eds.),Solid-stateChemical Sensors,AcademicPress, New York, 1985.
SMiddelhoek,Ed. ,Sensorsand Actuators, vol. 10, 1986.
F. Scheller, F. Schubert,D. Pfeiffer, R. Hintsche, I. Dransfeld, R. Renneberg,U. Wollenberger,K. Riedel,
M. Pavlova, M. Kuhn, H-G. Muller, P.M. Tan, W. Hoffmann and W. Moritz, Research and development
of biosensors, Analyst, U,653, 1989
M.A. Arnold and M.E. Meyerhoff, Recent advances in the development and analytical applications of
biosensingprobes, CRC Critical Reviews in Anal. Chem.,211,149, 1988.
15.

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Chemical sensors definitions and classification

  • 1. Pure&App/. Chern., Vol. 63, No. 9, pp. 1247-1250, 1991. Printed in Great Britain. @ 1991 IUPAC ADONIS 206922209100118Y INTERNATIONAL UNION OF PURE AND APPLIED CHEMISTRY ANALYTICAL CHEMISTRY DIVISION COMMISSION ON GENERAL ASPECTS OF ANALYTICALCHEMISTRY"? CHEMICAL SENSORS DEFINITIONS AND CLASSIFICATION Prepared for publication by ADAM HULANICKI', STANISEAW GEAB and FOLKE INGMAN2 'Department of Chemistry, University of Warsaw, Warsaw, Poland *Department of Analytical Chemistry, Royal Institute of Technology, Stockholm, Sweden *Membership ofthe Commissionduring the preparation of the report (1985-90) was as follows: 1985-87 Chairman: G. Ackermann (GDR); Secretary: D. Thorburn Burns (UK); Titular Members: St. Glab (Poland); F. Ingman (Sweden); D. L. Massart (Belgium); S. B. Sawin (USSR); L. Sommer (Czechoslovakia); Associate Members: D. Baylocq (France); A. Hulanicki (Poland); J. Incztdy (Hungary); W. E. van der Linden (Netherlands); M. Takagi (Japan); P. C. Uden (USA); G. Vigh (USA); E. V. Wanninen (Finland); B. D. Westerlund (Sweden); National Representatives:J. F. Desreux (Belgium); 0.Budevsky (Bulgaria); J. Garaj (Czechoslovakia). 1987-89 Chairman: D. Thorburn Burns (UK); Secretary: F. Ingman (Sweden); Titular Members: St. Glab (Poland); D. L. Massart (Belgium); L. Sommer (Czechoslovakia); P. C. Uden (USA); W. E. van der Linden (Netherlands); Associate Members: D. Baylocq (France); A. Marton (Hungary); H. Muller (GDR); S. B. Sawin (USSR); M. Takagi (Japan); G. Vigh (USA); E. V. Wanninen (Finland); B. D. Westerlund (Sweden); P. J. Worsfold (UK); National Representatives: J. F. Desreux (Belgium); 0. B. Budevsky (Bulgaria); J. Garaj (Czecho- slovakia);G. Ackermann (GDR);J. Incztdy (Hungary);A. Hulanicki (Poland);S. Ates (Turkey). 1989-91 Chairman: F. Ingman (Sweden); Vice-chairman: R. E. Van Grieken (Belgium); Secretary: W. E. van der Linden (Netherlands); Co-Secretary: C. L. Graham (UK); Titular Members: L. A. Currie (USA); St. Glab (Poland); W. Horwitz (USA); D. L. Massart (Belgium); M. Parkany (Switzerland); Associate Members: P. S. Goel (India); Y. Gohshi (Japan); H. Muller (GDR); M. Otto (GDR); G. J. Patriarche (Belgium); S. B. Savvin (USSR); J. W. Stahl (USA); P. J. Worsfold (UK); National Representatives: Tania M. Tavares (Brazil); L. Sommer (Czechoslovakia); D. Klockow (FRG); K. Danzer (GDR); J. InczBdy (Hungary); D. Thorburn Burns (UK); R. D. Reeves (New Zealand); A. Hulanicki (Poland); B. Schreiber (Switzerland); S . Ates (Turkey); G. Svehla (UK). tCommission title 1985-89: Commission on AnalyticalReactions, Reagents, and Separations Republication of this report is permitted without the need for formal IUPAC permission on condition that an acknowledgement, with full reference together with IUPAC copyright symbol (01991 IUPAC), is printed. Publication of a translation into another language is subject to the additional condition of prior approval from the relevant IUPAC National Adhering Organization.
  • 2. Chemical sensors: definitions and classification DEFINITIONS A chemicalsensoris a device that transformschemicalinformation,ranging from the concentration of a specific sample component to total composition analysis, into an analytically useful signal. The chemical information,mentioned above,may originatefrom a chemicalreaction of the analyte or from a physical property of the system investigated. A physical sensor is a device that provides information about a physicalproperty of the system. A chemical sensoris an essential componentof an analyzer. In additionto the sensor,the analyzermay contain devicesthat perform the followingfunctions:sampling,sampletransport, signalprocessing, data processing. An analyzer may be an essential part of an automated system. The analyzer working according to a sampling plan as a functionof time acts as a monitor. Chemical sensorscontain two basic functionalunits: a receptor part and a transducerpart. Some sensors may includea separator which is, for example,a membrane. In the recepror part of a sensor the chemical information is transformed into a form of energy which may be measured by the transducer. The transducer part is a device capable of transforming the energy carrying the chemical information about the sample into a useful analyticalsignal.The transduceras suchdoes not show selectivity. Thereceptorpart of chemicalsensorsmay be based upon variousprinciples: - physical, where no chemical reaction takes place. Qpical examples are those based upon measurementof absorbance,refractiveindex,conductivity,temperatureor mass change. - chemical, in which a chemical reaction with participation of the analyte gives rise to the analytical signal. - biochemical, in which a biochemical process is the source of the analytical signal. Qpical examples are microbial potentiometric sensors or immunosensors. They may be regarded as a subgroupof the chemical ones. Such sensorsare called biosensors. In some cases it is not possible to decide unequivocally whether a sensor operates on a chemicalor on a physical principle. This is, for example,the case when the signalis due to an adsorption process. Sensors are normally designed to operate under well defined conditions for specified analytes in certain sample types. Therefore, it is not always necessary that a sensor responds specifically to a certain analyte.Under carefully controlled operatingconditions,the analyte signal may be independentof other sample components, thus allowing the determination of the analyte without any major preliminary treatment of the sample. Otherwiseunspecificbut satisfactory reproducible sensors can be used in series for multicomponent analysis using a multivariate calibration software and signal processing. Such systemsfor multicomponentanalysis arecalled sensorarrays. CLASSIFICATION OF SENSORS The developmentof instrumentation,microelectronicsand computersmakes it possibleto design sensors utilizing most of the known chemical, physical and biological principles that have been used in chemistry. Chemicalsensorsmay be classifiedaccordingto the operatingprinciple of the transducer. 1.Oprical devicestransform changes of optical phenomena,which are the result of an interactionof the analyte with the receptor part. This group may be further subdivided according to the type of optical propertieswhich have been applied in chemicalsensors: a) absorbance,measured in a transparentmedium,causedby the absorptivity of the analyte itself or by a reaction with some suitableindicator. b) reflectanceis measured in non-transparentmedia, usually using an immobilizedindicator. c) luminescence,based on the measurementof the intensityof lightemitted by a chemicalreaction in the receptorsystem. 1248
  • 3. Chemical sensors: definitions and classification 1249 d) fluorescence, measured as the positive emission effect caused by irradiation. Also, selective quenching of fluorescencemay be the basis of suchdevices. e) refractive index, measured as the result of a change in solution composition. This may include also a surfaceplasmon resonanceeffect. f ) optothermaleffect, based on a measurementof the thermal effectcaused by light absorption. g) light scattering,based on effectscausedby particlesof definite sizepresent in the sample. The application of many of these phenomena in sensors became possible because of the use of optical fibres in various configurations. Such devices have also been called optodes. It should be emphasized that fibre optics now commonly used are only technical devices applicable in a large group of optical sensorswhich can be based on variousprinciples. 2. Electrochemical devices transform the effect of the electrochemical interaction analyte -electrode into a useful signal. Such effects may be stimulated electrically or may result in a spontaneous inter- actionat the zero-currentcondition.The followingsubgroupsmay be distinguished: a) voltammetricsensors, including amperometricdevices, in which currentis measured in the d.c. or a.c. mode. This subgroup may include sensors based on chemically inert electrodes, chemically active electrodes and modified electrodes. In this group are included sensors with and without (galvanic sensors)externalcurrent source. b) potentiometricsensors,in which the potential of the indicatorelectrode (ion-selectiveelectrode,redox electrode,metaVmeta1oxideelectrode)is measured againsta referenceelectrode. c) chemically sensitized field effect transistor (CHEMFET)in which the effect of the interaction between the analyte and the active coating is transformed into a change of the source-drain current.The interactionsbetween the analyte and the coating are, from the chemical point of view, similar to those foundin potentiometric ion-selectivesensors. d) potentiometric solid electrolyte gas sensors, differing from class 2b) because they work in high temperaturesolidelectrolytesand are usually appliedfor gas sensingmeasurements. 3. Electrical devices based on measurements, where no electrochemical processes take place, but the signalarisesfrom the changeof electricalpropertiescausedby the interactionof the analyte. a) metal oxide semiconductorsensors used principally as gas phase detectors,based on reversibleredox processesof analytegas components. b) organic semiconductor sensors, based on the formation of charge transfer complexes, which modify the chargecarrierdensity. c) electrolyticconductivity sensors. d) electricpermittivity sensors. 4. Mass sensitive devices transform the mass change at a specially modified surface into a change of a property of the supportmaterial. Themass changeis causedby accumulationof the analyte. a) piezoelectric devices used mainly in gaseous phase, but also in solutions, are based on the measurementthe frequency change of the quartz oscillator plate caused by adsorption of a mass of the analyteat the oscillator. b) surface acoustic wave devices depend on the modification of the propagation velocity of a generated acousticalwave affected by the depositionof a definitemass of the analyte. 5. Magnetic devices based on the change of paramagnetic properties of a gas being analysed.These are representedby certain types of oxygen monitors. 6. Thermometricdevices based on the measurement of the heat effects of a specific chemicalreaction or adsorption which involve the analyte. In this group the heat effects may be measured in various ways, for examplein the so called catalytic sensorsthe heat of a combustionreaction or an enzymaticreaction is measured by use of a thermistor. The devices based on measuring optothermal effects (If) can alternativelybe included in this group.
  • 4. 1250 COMMISSION ON GENERALASPECTS OF ANALYTICAL CHEMISTRY 7. Other physical properties as for example X-, p- or r- radiation may form the basis for a chemical sensorin casethey areused for determination of chemical compostion. This classification represents one of the possible alternatives. Sensors have, for example, been classified not according to the primary effect but to the method used for measuring the effect. As an example can be given the so-called catalytic devices in which the heat effect evolved in the primary process is measured by the change in the conductivity of a thermistor. Also, the electrical devices are often put into onecategory together with the electrochemical devices. Sensors have also been classified according to the application to detect or determine a given analyte. Examples are sensors for pH, for metal ions or for determing oxygen or other gases. Another basis for the classification of chemical sensors may be according to the mode of application, for example sensorsintended for use in vivo, or sensorsfor process monitoring and so on. It is, of course, possible to use various cassifications as long as they are based on clearly defined and logically arranged principles. The biosensors are not presented as a special class because the process on which they are based is, in general, common to chemical sensors. They may be also differentiated according to the biological elements used in the receptor. Those may be: organisms, tissues, cells, organelles, membranes, enzymes, antibodies, etc. The biosensors may have several enzymatic systems coupled which serve for amplificationof the signal. Various sensorsmay be combined in sets which are often called multisensors. GENERAL REFERENCES 1. Proceedings of the International Meeting on Chemical Sensors, Fukuoka, Japan, September 19-22, 1983, Editors: T. Seyma, K. Fueki,J. Shiokawa and S. Suzuki, Elsevier-Kodanscha, Amsterdam and Tokyo, 1983. H. Wohltjen, Chemical Microsensorsand Microinstrumentation,Anal. Chem.,%,87A, 1984. W.R. Seitz, Chemical SensorsBased on Immobilized Indicators and Fibre Optics, CRC CriticalReviews in Anal. Chem., 19,135, 1988. M. Thompson and U. J. Krull, Biosensors and Bioprobes, Trends in Anal. Chem.,3, 173, 1984. T.E. Edmonds (ed.),Chemical Sensors,Blackie and Sons Ltd., London, 1988. A.P.F. Turner, I. Karube and G.S. Wilson (eds.), Biosensors. Fundamentals and Applications,Oxford UniversityPress,New York, 1987. R. Niessner, Chemische Sensoren:Principienund Anwendungen in Analytiker Taschenbuch,vol. 7. (eds.: W. Fresenius et. al.) SpringerVerlag,Berlin, 1988,p. 55. D. Schuetzle, R. Hammerle and J. Butler (eds.), Fundamentals and Applications of Chemical Sensors, ACS Symposium Series, 309 AmericanChemical Society, 1986. 2. 3. 4. 5. 6. 7. 8. 9. W. Gopel, Entwicklung Chemischer Sensoren. Empirische Kunst oder systematische Forschung? Techn. Messen,2,47,92, 175,1985. 10. 11. 12. 13. 14. C. Nylander,Chemical Sensorsand Biological Sensors,J. Phys. Sci. Instr., Is,736, 1985. J. Janata and A. Bezegh,Chemicalsensors,Anal.Chem.,@, 62R, 1988. J. Janata, R.J. Huber (eds.),Solid-stateChemical Sensors,AcademicPress, New York, 1985. SMiddelhoek,Ed. ,Sensorsand Actuators, vol. 10, 1986. F. Scheller, F. Schubert,D. Pfeiffer, R. Hintsche, I. Dransfeld, R. Renneberg,U. Wollenberger,K. Riedel, M. Pavlova, M. Kuhn, H-G. Muller, P.M. Tan, W. Hoffmann and W. Moritz, Research and development of biosensors, Analyst, U,653, 1989 M.A. Arnold and M.E. Meyerhoff, Recent advances in the development and analytical applications of biosensingprobes, CRC Critical Reviews in Anal. Chem.,211,149, 1988. 15.