GB2234061A - Water monitor - Google Patents

Water monitor Download PDF

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Publication number
GB2234061A
GB2234061A GB8915380A GB8915380A GB2234061A GB 2234061 A GB2234061 A GB 2234061A GB 8915380 A GB8915380 A GB 8915380A GB 8915380 A GB8915380 A GB 8915380A GB 2234061 A GB2234061 A GB 2234061A
Authority
GB
United Kingdom
Prior art keywords
water
organic liquid
light
infra
floc
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
GB8915380A
Other versions
GB8915380D0 (en
GB2234061B (en
Inventor
Colin Arthur Baker
Brian Phillip Stimpson
Robert Andrew Haine
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
UK Atomic Energy Authority
Sellafield Ltd
Original Assignee
British Nuclear Fuels PLC
UK Atomic Energy Authority
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 British Nuclear Fuels PLC, UK Atomic Energy Authority filed Critical British Nuclear Fuels PLC
Priority to GB8915380A priority Critical patent/GB2234061B/en
Publication of GB8915380D0 publication Critical patent/GB8915380D0/en
Publication of GB2234061A publication Critical patent/GB2234061A/en
Application granted granted Critical
Publication of GB2234061B publication Critical patent/GB2234061B/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/18Water
    • G01N33/1826Water organic contamination in water
    • G01N33/1833Oil in water
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N21/47Scattering, i.e. diffuse reflection
    • G01N21/49Scattering, i.e. diffuse reflection within a body or fluid
    • G01N21/53Scattering, i.e. diffuse reflection within a body or fluid within a flowing fluid, e.g. smoke
    • G01N21/532Scattering, i.e. diffuse reflection within a body or fluid within a flowing fluid, e.g. smoke with measurement of scattering and transmission
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/18Water
    • G01N33/1813Water specific cations in water, e.g. heavy metals
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N15/00Investigating characteristics of particles; Investigating permeability, pore-volume, or surface-area of porous materials
    • G01N2015/0023Investigating dispersion of liquids
    • G01N2015/003Investigating dispersion of liquids in liquids, e.g. emulsion
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N21/25Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
    • G01N21/31Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
    • G01N21/314Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry with comparison of measurements at specific and non-specific wavelengths
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A20/00Water conservation; Efficient water supply; Efficient water use
    • Y02A20/20Controlling water pollution; Waste water treatment

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Food Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Investigating Or Analysing Materials By Optical Means (AREA)

Abstract

An instrument is provided for monitoring a stream of water in a glass tube (12) for the presence of both ferric floc and an organic liquid immiscible with water. Infra-red light from a source (14) is passed into the water, and the scattered light is monitored with a detector (22). Green light from a source (16) is passed through the water and a detector (26) monitors the transmitted intensity. From these two measurements the concentrations of the ferric floc and of the organic liquid can be calculated. To obtain reliable measurements, means (20; 15, 25, 28) are provided to enable any changes in the emitted light intensities or detector efficiencies to be taken into account or eliminated. The organic liquid may be kerosene. <IMAGE>

Description

Water Monitor The invention relates to a method and an instrument for monitoring water to detect small quantities of organic liquid.
A bilge-water monitor is commercially available (from Babcock-Bristol Ltd., of Purley Way, Croydon, England) which monitors for small quantities of oil in water (for example about 10 parts per million (ppm)) by measuring the extent to which infra-red light is scattered when passed through a sample of bilge-water.
According to the present invention there is provided an instrument for monitoring for the presence in water of both ferric floc and an organic liquid immiscible with water, the instrument comprising means for passing infra-red light through the water, and first sensor means for sensing the extent to which the infra-red light is scattered by the water, means for passing green light through the water, and second sensor means for sensing the extent to which the green light is transmitted through the water, and means responsive to signals from both the first and the second sensor means to determine the concentrations of both the organic liquid and of the ferric floc in the water.
The organic liquid may be kerosene. The instrument is applicable where the floc concentration is typically in the range 0 to 250 ppm, and where the kerosene concentration is in the range 0 to 250 ppm. The water may be pure, or may contain chemicals in solution such as nitric acid which have negligible effect on the scattering or transmission of the light passed through the water.
It has been discovered that the oil-sensitive bilge-water monitor mentioned above can be used to monitor kerosene, but that it also detects ferric floc and is approximately as sensitive to ferric floc as it is to kerosene. Consequently if both ferric floc and kerosene may be present then measurements obtained with that monitor do not enable the concentration of either kerosene or of ferric floc to be determined independently. Using green light, the absorption is principally due to the ferric floc. Hence by measuring the degree of scattering of infra-red and the transmission of green light, the concentrations both of ferric floc and of kerosene can be determined independently.
The invention also provides a method for monitoring for the presence in water of both ferric floc and and immiscible organic liquid, the method comprising causing infra-red light and green light to propagate through the water, measuring the extent to which the infra-red light is scattered and the extent to which the green light is transmitted by 'the water, and hence determining the concentrations of the ferric floc and of the organic liquid in the water.
The invention will now be further described, by way of example only and with reference to the accompanying drawings, in which: Figure 1 shows a diagrammatic view of a water-monitoring instrument; and Figure 2 shows graphically the variations of signals in the circuit of Figure 1 for variations in floc and kerosene concentration.
Referring to Figure 1, the instrument 10 includes a glass tube 12 through which water is caused to flow, and monitors the water for both ferric floc and odourless kerosene. The instrument 10 comprises an infra-red light emitting diode 14 and a green light emitting diode 16 each connected electrically to respective terminals of a power supply 18 and mounted on or adjacent to the tube 12 so as to send a beam of radiation diametrically across the tube 12. Directly opposite the diode 14 is a light sensitive diode 20 arranged to receive the infra-red light transmitted through the water, and arranged at right angles to the transmitted beam is a second light sensitive diode 22 to receive infra-red light scattered by the water.
Signals from these diodes 20 and 22 are amplified and then compared by a unit 24 which provides an output signal A representing the ratio of the scattered light to the transmitted light. Similarly, a light sensitive diode 26 is arranged directly opposite the diode 16, so as to receive the green light transmitted through the water and the signal from this diode 26 is amplified and then compared by a unit 30 to the corresponding signal when the water is clean; the unit 30 provides an output signal B representing the natural logarithm of the ratio of the transmitted light with clean water to the transmitted light as observed.Connected electrically in series with the diode 16 is another green light emitting diode 15, identical with the diode 16; this transmits light to a light sensitive diode 25, whose signals are amplified by a unit 28 and fed back to the power supply 18 to control the current supplied to the diodes 15 and 16 and so to ensure that the green light emission does not vary for example with the temperature of the diodes 15 and 16.
The output signal from the unit 24 represents the extent to which the water scatters the infra-red light, and is substantially unaffected by any variation in the brightness of the emitted light beam from the diode 14.
The feedback circuit 15, 25, 28 ensures that there is substantially no variation in the brightness of the light beam from the diode 16, so the output signal from the unit 30 accurately represents the extent to which the transmission of green light is affected by the water.
The signals from the units 24 and 30 are received by a hard-wired calculating unit 32 which determines from them the concentrations of ferric floc and of kerosene, providing signals to two display units 34 and 36 which indicate respectively the concentration of ferric floc and the concentration of odourless kerosene in the water.
Referring to Figure 2, this shows graphically the variation of the output signals from the units 24 and 30 (signals A and B respectively), with either kerosene or ferric floc, but not both, in the water; the plotted values were obtained from experimental measurements. It will be apparent that the scattering of the infra-red light (A) is directly proportional to the concentration of either ferric floc or of kerosene, though kerosene scatters infra-red light about one and a half times more than does ferric floc. The decrease in the transmission of green light expressed logarithmically (B) is also directly proportional to the concentration of either ferric floc or of kerosene, but kerosene affects the transmission less than a fifth as much as does ferric floc.When both kerosene and ferric floc are present, their effects on both the scattering of infra-red light and the transmission of green light are merely additive. Thus for a kerosene concentration k and a ferric floc concentration f the values of these signals are given by: A = ak + bf B = ck + df where a, b, c and d are the gradients of these calibration graphs. Knowing the values of the gradients a, b, c and d, unknown values of k and f can readily be determined from measurements of A and B by mathematical solution of these two simultaneous algebraic equations.
It will be appreciated that the concentrations can be calculated using analogue signals and a hard-wired calculation circuit 32 as described above. Alternatively amplified signals from the diodes 20, 22, 26 and 25 may be digitized, and all the calculations performed digitally, using a microprocessor for example. In this case the feedback from the amplifier 28 to the power supply 18 can be dispensed with, and instead the digitized signal from the diode 25 used to normalize the signal from the diode 26 to take into account variations in the light emitted by diodes 15 and 16. To obtain accurate measurements it is necessary to take into account any variations in the brightness of the emitted light beams, and in the method described above this is done for the infra-red by measuring the transmitted beam using diode 20, while it is done for the green by measuring with the diode 25 the brightness of the light emitted by the diode 15 in series with the diode 16. If light sources other than light-emitting diodes were to be used instead, other monitoring techniques might be practical; for example a light beam from a laser might be passed through a beam splitter before entering the water, and the intensity of the beam split off by the beam splitter be monitored.

Claims (5)

Claims
1. An instrument for monitoring for the presence in water of both ferric floc and an organic liquid immiscible with water, the instrument comprising means for passing infra-red light through the water, and first sensor means for sensing the extent to which the infra-red light is scattered by the water, means for passing green light through the water, and second sensor means for sensing the extent to which the green light is transmitted through the water, and means responsive to signals from both the first and the second sensor means to determine the concentrations of both the organic liquid and of the ferric floc in the water.
2. An instrument as claimed in Claim 1 also comprising means to ensure that the determined concentrations are not affected by any variations in the intensities of the emitted lights.
3. A method for monitoring for the presence in water of both ferric floc and immiscible organic liquid, the method comprising causing infra-red light and green light to propagate through the water, measuring the extent to which the infra-red light is scattered and the extent to which the green light is transmitted by the water, and hence determining the concentrations of the ferric floc and of the organic liquid in the water
4. An instrument for monitoring for the presence in water of both ferric floc and an organic liquid immiscible with water, substantially as hereinbefore described with reference to, and as shown in, Figure 1 of the accompanying drawings.
5. A method for monitoring for the presence in water of both ferric floc and immiscible organic liquid, substantially as hereinbefore described with reference to, and as shown in, the accompanying drawings.
GB8915380A 1989-07-05 1989-07-05 Water monitor Expired - Fee Related GB2234061B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB8915380A GB2234061B (en) 1989-07-05 1989-07-05 Water monitor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB8915380A GB2234061B (en) 1989-07-05 1989-07-05 Water monitor

Publications (3)

Publication Number Publication Date
GB8915380D0 GB8915380D0 (en) 1989-08-23
GB2234061A true GB2234061A (en) 1991-01-23
GB2234061B GB2234061B (en) 1993-03-31

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Family Applications (1)

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GB8915380A Expired - Fee Related GB2234061B (en) 1989-07-05 1989-07-05 Water monitor

Country Status (1)

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GB (1) GB2234061B (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2282880A (en) * 1993-10-18 1995-04-19 Welsh Water Enterprises Ltd Apparatus for measuring characteristics of a liquid
WO2000058714A1 (en) * 1999-03-26 2000-10-05 Cranfield University Detection of liquids
GB2355524A (en) * 1999-10-18 2001-04-25 Siemens Plc Device for measuring colour and turbidity in a liquid sample
US7242001B1 (en) 1999-10-18 2007-07-10 Censar Technologies, Inc Device for measuring water quality

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2282880A (en) * 1993-10-18 1995-04-19 Welsh Water Enterprises Ltd Apparatus for measuring characteristics of a liquid
GB2282880B (en) * 1993-10-18 1997-07-23 Welsh Water Enterprises Ltd Apparatus for measuring characteristics of a liquid
US5864140A (en) * 1993-10-18 1999-01-26 Acer Consultants Limited Apparatus for measuring characteristics of a liquid
WO2000058714A1 (en) * 1999-03-26 2000-10-05 Cranfield University Detection of liquids
US6717658B1 (en) 1999-03-26 2004-04-06 Cranfield University Detection of liquids
GB2355524A (en) * 1999-10-18 2001-04-25 Siemens Plc Device for measuring colour and turbidity in a liquid sample
US7242001B1 (en) 1999-10-18 2007-07-10 Censar Technologies, Inc Device for measuring water quality

Also Published As

Publication number Publication date
GB8915380D0 (en) 1989-08-23
GB2234061B (en) 1993-03-31

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PCNP Patent ceased through non-payment of renewal fee

Effective date: 20020705