WO2000004351A2 - Infrared radiation source and its application for gas measurement - Google Patents
Infrared radiation source and its application for gas measurement Download PDFInfo
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- WO2000004351A2 WO2000004351A2 PCT/NO1999/000240 NO9900240W WO0004351A2 WO 2000004351 A2 WO2000004351 A2 WO 2000004351A2 NO 9900240 W NO9900240 W NO 9900240W WO 0004351 A2 WO0004351 A2 WO 0004351A2
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- infrared radiation
- radiation source
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Classifications
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01J—MEASUREMENT OF INTENSITY, VELOCITY, SPECTRAL CONTENT, POLARISATION, PHASE OR PULSE CHARACTERISTICS OF INFRARED, VISIBLE OR ULTRAVIOLET LIGHT; COLORIMETRY; RADIATION PYROMETRY
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- G01J3/02—Details
- G01J3/10—Arrangements of light sources specially adapted for spectrometry or colorimetry
- G01J3/108—Arrangements of light sources specially adapted for spectrometry or colorimetry for measurement in the infrared range
Definitions
- Infrared radiation source and its application for gas measurement This invention concerns electrically pulsed infrared radiation sources, and discloses how, with simple means, one may specify and improve their performance far beyond what is possible in the prior art. This shall offer considerable advantages when utilizing such radiation sources in connection with gas sensors in particular, which by using infrared radiation sources according to the invention may be made better, simpler and less expensive compared to what has been possible earlier.
- Infrared (IR) sensors for gas comprise both IR sources and IR detectors.
- IR detectors normally react only on changes in IR radiation. In connection with technical measurements this is traditionally established by pulsing the radiation by means of a so-called "chopper", a rotating wheel with holes that chop the radiation from a constant (CW) source. This generates large temperature amplitudes between the hot source and the cold chopper blade, as seen from the IR detector.
- the radiation pulses may then be exactly calculated, because the temperatures will be known both for the IR source and the chopper blade. However, the pulses are locked onto one given frequency only, and the technique depends on expensive, inflexible and often delicate equipment with moving parts that are not adapted to modern electronic technology.
- IR detectors convert the IR signal into electrical signals with detector-specific responsivities R [V/W]. Next the electrical signals are subject to standard electronic amplification and signal treatment. The IR signal increases with the strength of the IR pulses. Therefore, large temperature amplitudes ⁇ rfor the source are essential. The measurements, however, are limited by noise, too, which is chiefly caused by the detector. In this respect, IR detectors are defined by their "Noise-Equivalent-Power", NEP, which increases with the square root of the electrical bandwidth ⁇ of the signal electronics; NEP ⁇ ( Af) 1 ' 2 .
- the quality of an IR measurement is given by the signal-to-noise ratio S/N, which to good measure will be proportional to AT and inversely proportional to ( Af) 1 ' 2 ; i.e., S/N ⁇ AT/(Af)' /2 .
- S/N signal-to-noise ratio
- 5,220,173 opens for a possible solution to those problems, through its disclosure of an electrically pulsed thermal IR source which is cooled by thermal radiation between the pulses.
- Radiation-cooled IR sources may achieve temperature variations of the order of 100 K or more, with correspondingly strong IR pulses.
- the possibility then also exists to perform measurements by means of single pulses at chosen times, with the source turned off in between pulses. This may afford good temporal resolution and low current loads, with IR signals that appproach those obtained with choppers.
- Said U.S.Patent only provides the necessary conditions for the manufacture of a pulsed, radiation-cooled thermal IR source.
- the patent gives no answer as to how one may achieve temperature amplitudes of prescribed, preferred magnitudes, nor does it give any advice on which pulse lengths may be used.
- Such information is vital in order to produce IR sources whose performance and yield are determined from the requirements set by concrete applications, for example, when making real IR sensors which are optimized in relation to signal strength, temporal resolution, S/N ratio etc for a given technical measurement task.
- the present invention takes as its starting point the said U.S.Patent 5,220,173, and teaches how one may produce IR sources with powerful and entirely specified single IR pulses.
- the IR source is made from an electrically conductive foil shaped material, and that it radiates from a higher temperature T m which is maintained for a certain element of time, subject to excitation by a pulse of electric current from a suitable electric drive circuit.
- T m which is maintained for a certain element of time, subject to excitation by a pulse of electric current from a suitable electric drive circuit.
- T m which is maintained for a certain element of time
- T a pulse of electric current from a suitable electric drive circuit.
- the temperature is set depending on the spectral region which the source is to cover, often T trash, may be found in the region 800 - 1,000 K.
- the source When the current pulse is switched off, the source supposedly becomes rapidly cooled by a large, predetermined temperature amplitude ⁇ Jto a lower temperature T 0 , to produce a preferred magnitude of the IR signals.
- cooling occurs by means of thermal radiation, according to the said U.S.Patent No 5,220,173.
- the foil shaped material is assumed to have thickness d. Cooling the source across a temperature interval AT from T m to T 0 then requires that an amount of thermal energy E s be removed from the source, where
- Relation (3) discloses how pulsed, radiation-cooled IR sources must be made in order to make temperature amplitudes of AT dimension feasible at pulse lengths ⁇ .
- the necessary and sufficient physical requirements and conditions for producing radiation-cooled, pulsed IR sources thus are determined by those combinations of temperature amplitudes and pulse lengths which the sources are to produce.
- Relation (3) is new and entirely general, and is valid for any areal shape and size of the source, because all parts of the source surface are locally cooled by thermal radiation transversely to the surface and independently of heat conduction along the surface. When made according to relation (3), therefore, IR sources with large emitting surfaces may be pulsed as rapidly and as often as small sources; with previous, conduction-cooled sources this could not be done. Relation (3) enters into claim 1 as the characterizing feature of the present invention.
- the source may also be formed in such a way that the foil shaped material is either heated in its entirety, or that only certain parts of the source become heated to the actual temperatures; in any case it is the thickness of those parts of the source which are to be heated to the temperature T Tha, that occurs in relation (3) and in the corresponding expression in claim 1.
- Claim 1 opens up for the manufacture of electrically pulsed IR sources which satisfy stated, preferred technical data and specifications, in a manner similar to IR detectors and other modern optical and electronic components and products.
- this makes it possible to develop simple and inexpensive pulsed IR sensors that are adapted to particular applications, and whose performance may be calculated and specified even in the design phase.
- Such sensors by themselves represent a considerable novelty as compared with the prior art.
- the challenge will be to manufacture, to an industrial scale, such IR sources that can withstand those large thermal and mechanical strains which may arise, when they become subjected to frequent, repeated temperature excursions of 100 K or more. For most materials, this may bring about fracture due to buckling.
- the source may twist and bend as a result of heating, which produces an unstable source with shifting IR illumination of the IR detector.
- the invention has as its aim to provide solutions for all such tasks and problems, by creating a technological platform for industrial manufacture of improved IR sources, both as special, self-contained products and as essential, specified components in equipment that employs the source and its qualities in new and advanced methods and sensors for IR measurements of gas.
- the invention is to be more closely presented and described, by means of references to and comments on the patent claims and by referring, in particular, to the figures, in which all shapes and dimensions may be distorted in the interest of illustrating a point, and where
- Figure 1 shows a preferred mounting of the IR source
- Figure 2 shows a preferred shape of the IR source
- Figure 3 shows a joint mounting of several IR sources
- Figure 4 shows an example of an encapsulated IR source
- Figure 5 shows a preferred pulse of current with the resulting IR pulse
- Figure 6 shows in principle the design of an IR gas sensor
- Figure 7 shows the use of two or more IR sources with a spectrally dispersive element.
- the crucial feature is the relation - identical with (3) - which imposes an upper limit on the thickness of the foil shaped material of the source element, in order for the IR source to be produced in accordance with the specifications that are required in regard to technical performance.
- the said relation includes the material parameters ⁇ , C and p, which most often allow only limited latitude; ⁇ is chosen to be as high as practically possible in each case, normally a value between 0.5 and 1 , and the product Cp for most regular materials has a value in the range 2 - 4 JK" 1 cm 3 .
- the emission temperature may be around 1 ,000 K, which produces a broad thermal spectrum from the source with a maximum near 3 ⁇ m wavelength and well suited for the spectra of most relevant gases.
- T Tha 1,000 K
- the requirement on the IR source thickness thus may be expressed as
- the pulse length too, will have to be increased, to 50 ms or more.
- high temporal resolution and large IR signals cannot be combined without further measure.
- limits on the pulse length are set not only by the requirements of time resolution.
- the frequency spectrum Af determines the width of the noise spectrum in the measurements.
- the noise shall increase inversely with the square root of the pulse length, NEP ⁇ ( ⁇ /) l 2 ⁇ ( ⁇ ) "1/2 , to make the S/N-relation vary as S/N ⁇ AT' ( ⁇ ) 1/2 .
- NEP ⁇ ( ⁇ /) l 2 ⁇ ( ⁇ ) "1/2 to make the S/N-relation vary as S/N ⁇ AT' ( ⁇ ) 1/2 .
- Figure 1 depicts an IR source as mounted with its ends onto two fastening arrangements 14 and 15, - which may also serve as electrical contacts -, in such a way that the end surfaces of the source make an angle with each other as seen from the side.
- the source then shall be standing as a curve-shaped bridge between the fixtures.
- Such a mounting solves the problem of breakage due to buckling when the source becomes repetitively heated and cooled with large temperature amplitudes.
- the source may be mounted so as to make the freely suspended part of the curve lie wholly inside the corresponding circular sector whose tangents coincide with those of the source at the fixture contacts, however, without making any abrupt changes in curvature.
- the fastening arrangements ought to be fixed in space, and the source should be permanently and solidly attached to those, e.g., by the use of screws, squeezing, welding or similar means. This also avoids that the source may bend and twist during a pulse of current.
- the source's reaction upon the heating will then be limited to microscopic movements of its middle parts, back and forth in axial direction facing the detector. This takes place without any mechanical stress being induced in the material.
- the source constitutes a geometrically and postionally stable shape, with a radiation lobe that does not change during the pulse.
- the source In order to locate the heating to a prefe ⁇ -ed part of the source, most often near the middle of its length extension, the source may be given a weakly tapering shape towards the centre of the hot region. Thereby the thermal emission shall be permanently concentrated to a predetermined part of the source, shown as item 21 in Figure 2. Outside of this region, the width may be constant, or it may widen into two broader ends 22 and 23 as is also shown in Figure 2. Both alternatives are contained in claim 4. Since the local electrical heating decreases with the square of the width, a solution as illustrated in the said figure also serves to reduce heat losses caused by thermal conduction into the fixtures. Moreover, the mechanical position of the source becomes further stabilised.
- IR sources mounted closely together, either in a row or in a two-dimensional matrix, as illustrated in Figure 3 and disclosed in claim 6. Electrically these may then be coupled so as to make two or more source elements be simultaneously excited, e.g., to assemble a particularly large and powerful IR source. Alternatively, the source elements may also be coupled in such a way that one or more elements are excited independently of other elements, for instance, in time multiplexing of different spectral IR pulses, or in order to simulate a thermally variable scene or picture.
- Such embodiments of claim 6 are disclosed in claims 7 and 8.
- Claims 9 - 13 disclose a selection of different materials that may be used for making the IR source.
- Certain metals, alloys and metallic glasses as disclosed in claim 9 exist industrially as rolled foils in micron thicknesses.
- nickel-chromium-iron based alloys are made to be used in extreme thermal environments, and often have high emissivities in their natural state.
- metallic glasses many ceramic materials, too, may be made with predetermined electrical conductivities. Ceramics may be deposited from liquid phase into preferred shapes and thicknesses, which may be exploited to make IR sources according to claim 10.
- IR sources made from semiconductor materials according to claim 11 may be an obvious choice, particularly silicon but others, too, which let themselves to doping and treatments with etching and other techniques into preferred shapes etc.
- carbon based chemistry is rapidly developing, with new kinds of materials comprising fullerenes as well as carbon-based, diamond-type networks and other formats that may be used for making IR sources as disclosed in claim 12.
- Porous materials as disclosed in claim 13 represent a special alternative, because low density (i.e., small p) and large mechanical strength per square weight may allow shorter IR pulses to be obtained than can be had with homogeneous materials, for similar temperature amplitudes and physical thicknesses.
- the disclosed materials may have low emissivities in their natural state.
- High emissivity is important to obtain fast and powerful radiative cooling and strong IR signals.
- the emissivity ⁇ enters into the characterizing relation of claim 1.
- the emissivity may be improved to reach nearly its theoretically maximum value.
- a multitude of established industrial methods exist, such as, for example, chemical etching and ion/plasma treatment in vacuo, which may to some extent also be arranged to impart a systematic shape to the texture to obtain special effects.
- FIG. 4 shows an example of an IR source 40 mounted in an encapsulation 41 with two windows 42 and 43, and with electrical feed-throughs 44 and 45 for the supply of electrical current to the source.
- This solution is disclosed in claim 15, comprising an encapsulation with IR transparent windows adapted to at least one of opposite faces of the source.
- Another solution is disclosed in claim 16, in which the encapsulation has a bulb- or cylinder-like shape made from IR transmitting glass or other IR transparent material, with remaining remedies as in claim 15. Variants of different solutions may also be practicable.
- the IR pulses in question consist of three distinct phases: A heating phase, an emission phase and a cooling phase.
- a heating phase In order to achieve well-defined IR pulses, it is preferable to make the source heat rapidly to its operating temperature for each pulse. This may be obtained by the use of current pulses with a first part that carries a high current, and whose energy contents at least matches E s of equation (2) above; indeed, if the heating and cooling phases are approximately of equal duration, this initial part of the current pulse actually must contain an amount of energy quite close to 2 E s .
- the first part of the current pulse is adjusted to bring the source to its operating temperature T m . Thereafter, the current is reduced to a constant, lower level which serves to maintain the operating temperature. This solution is disclosed in claim 17.
- Figure 5 shows an example of such a preferred current pulse 53, and the resulting temperature history 54 of the source.
- the duration 55 of the constant level of the current pulse is adapted to the desired length ⁇ of the IR pulse. Since the source does not become further heated during the emission phase, essentially all electrical energy that is supplied to the source in this phase becomes radiated off as thermal energy. This secures a high energy efficiency. When the current pulse is switched off, the thermal energy that was stored in the source during the heating phase, becomes quickly removed by continued radiation, which produces a short cooling phase with strong initial cooling that weakens as the temperature keeps falling.
- Claim 18 discloses a method for pulse-wise identification, measurement and/or warning of gas by means of one or more IR sources according to the invention.
- the method is distinct from similar methods that are applied in prior-art IR sensors, in that the measurements are made in a pulse-wise manner using a pulsed IR source which has been produced in accordance with the present invention. This imposes certain limitations on the pulse lengths that may be used in the method.
- Figure 6 shows how the method is in principle carried out, by means of an IR source 61 that is excited by an electrical drive circuit 62, and where the IR radiation is guided via an optical element 63 through an open or enclosed volume of gas 64 and a spectrally selective element 65 onto an IR detector 66, followed by electronic equipment 67 for the amplification, treatment and/or presentation of the resulting signals.
- the order of the individual components in Figure 6 is insignificant and may be changed as desired.
- an IR source that has been manufactured according to claim 1 from a material with given values of C, p and ⁇ , and which is characterized by an actual and concrete thickness dute as one of its crucial specifi
- the method will be characterized by deciding on a temperature T m and a temperature amplitude ⁇ T, at which the source is to be operated.
- AT should preferentially be chosen to be larger than 100K.
- pulse lengths ⁇ t may be used for those measurements that the method is to perform.
- the method is characterized by being practised with those pulse lengths ⁇ , which, for the actual, existing IR source at hand and in accordance with relation (5), may at all be allowed for radiation-cooled IR sources that are manufactured according to the invention and with the chosen values for the temperature T Tin, and the temperature amplitude AT, of the IR source.
- the pulse lengths ⁇ that result from this are initially too long, compared to the time resolution that has been set for the measurements, an optimization has to be made by choosing other values for T m and/or ⁇ J, to the extent that such is compatible with the technical parameters and specifications for the actual materials and measurements.
- Claim 19 specifies the method even further. With reference to Figure 5. This happens through a summation of the electrical signals from the IR detector, inside an interval of time 51 called r, when the source radiates from the lower temperature level T 0 , and inside a similar time interval 52 called T 2 and which is less than or equal to the pulse length ⁇ personally when the IR source radiates from the higher temperature level T,hiel.
- T 1 an interval of time 51
- T 2 a similar time interval 52
- such asurment technique that operates inside given time intervals is termed "box-car integration".
- the method is complementary to that which is used in existing IR sensors, where signals are summed along a frequency axis and inside a given frequency interval at a certain modulation or chop frequency, whereas in the method according to claim 19 signals are summed inside a given time interval along a time axis.
- the difference in summed signals between the two time intervals is used as a measure of the amount of pulse-wise IR radiation which illuminates the actual IR detector, in analogy with what is otherwise common technology.
- T may be an advantage to make T, as large as possible, within the limits that are set by the temporal development between two consecutive pulses.
- Claim 20 discloses a sensor for the concrete embodiment of the method disclosed in claim 18.
- the sensor may comprise those same components that are cited in the method discussed in connection with claim 18 above.
- the sensor comprises an IR source that has been manufactured according to claim 1 , and which is, among other factors, characterized by an actual and concrete thickness d 0 as one of its crucial specifications.
- the IR source is operated with a definite temperature amplitude AT, at a higher temperature level T Titan, and with pulse lengths ⁇ , that satisfy relation (5), however, in which AT, as well as T Titan, and ⁇ , may have been subject to the eventual optimization that is disclosed in claim 18 as a part of adapting the method to the actual measurement task.
- the method disclosed in claim 18 thus serves to define the operational parameters for that particular IR source which is included in the sensor disclosed in claim 20, and thereby to define the necessary conditions that enables the sensor to perform those measurement tasks that are to be solved.
- a sensor has been disclosed in accordance with claim 20, which in addition embodies the method disclosed in claim 19.
- the sensor is adapted to comprise equipment for "box-car" integration of signals inside the said time intervals T, and F 2 , and to register or calculate the difference between those integrated signals as a measure of the amount of IR radiation that illuminates each single detector through the said volume of gas.
- claim 21 discloses one or more infrared narrow-band filters to be used, adapted to the gases in question.
- the filters may in principle be situated anywhere between the source and the detector. At least one filter is required for each gas to be measured; in addition, it is advantageous to employ at least one extra filter that does not coincide with the spectra of any of the gases that may be present: Said extra filters are used to establish a zero reference for the measurements, in regard to external factors other than gas and which may be assumed to influence all spectral measurements to the same extent, as for example dust accumulation on lenses and windows.
- a dispersive element as for instance a prism or an optical grating.
- a dispersive element as for instance a prism or an optical grating.
- Claim 23 discloses the use of one or more such dispersive elements, including a spherical infrared-optical grating.
- a spherical infrared-optical grating The latter alternative is illustrated in Figure 7, where one or more IR sources 71 illuminate a detector 72 through a narrow slit or aperture 73 via a spherical grating 74.
- the spherical grating also serves in a manner resemblant of a lens, to focus the radiation from the IR sources onto the detector.
- the physical width of the aperture may then be adapted to the spectral width of the gas spectra with high accuracy, and often far better than with narrow-band filters.
- different spectral components shall pass through the aperture, depending on the position of each IR source relative to the grating.
- dispersive elements tend to be considerably more expensive than spectral filters, and so may be mostly relevant for more costly multigas sensors.
- Claim 24 discloses a sensor in which one or more IR sources illuminate two or more IR detectors.
- one IR source may illuminate two detectors simultaneously, each of the detectors being equipped with its own IR filter for gas measurement and reference purposes, respectively. This may be a relevant solution for a simple and inexpensive single- gas sensor with reference measurement. Other combinations comprising several sources and/or detectors may be of interest, too, for special purposes.
- a sensor in which a single detector is illuminated by several IR sources, which are pulsed at different times.
- time multiplexing may be executed by means of a spherical grating as illustrated in Figure 7, in which the slit 73 has been placed in one focal point of the grating and the IR sources 71 are situated along a focal line on the other side of the grating.
- Each IR source then illuminates the detector with its own distinct spectral IR pulse at distinct times.
- a common reference detector on the rear side of the IR sources one may then also be able continuously to correct for any variations in radiation from one or more sources.
- IR detectors normally are quite small, of the order of mm 2 , so that most often optics will be required to collect a sufficient amount of radiation from the IR source.
- IR sources that may be pulsed as quickly and as often as small sources. With only a short distance to the IR source, the detector thus shall see the source at a relatively large solid angle. Even without optics, the detector may then intercept enough radiation for the measurements to be made.
- the optical arrangements that are mentioned in claims 18 and 20 then may simply consist of free and unobstructed propagation through the gas volume.
- Claim 26 discloses a sensor that is made in this way. It may very easily be adapted to employ several detectors for one and the same source. When it comes to measurements of larger gas densities, which require short paths through the gas volume, designs according to claim 26 may come to be preferred; this will make the sensor particularly robust against mechanical faults and misalignments in the mounting of components during production.
- thermopile detectors essentially a row of thermocouples connected in series - are particularly interesting. They are cheap and simple, but have low sensitivities and higher noise levels compared with the semiconductor detectors. On the other hand, they have no 1/f noise, because they are pure voltage generators.
- thermopile detectors are ideally suited in sensors that apply the present IR sources, which according to the analysis presented above may appropriately be pulsed with relatively long pulses at correspondingly low frequencies.
- Claim 27 thus discloses the use of thermopile detectors in sensors according to the invention. For simple, single gas sensors in particular, the use of such detectors may make the sensors sufficiently inexpensive to open up new and large markets for IR measurement and warning of gas.
- the sensors are arranged to execute the measurements in a single IR pulse, which has been adapted to the technical demands of the task in accordance with claims 18 - 21.
- it may be an additional advantage to sum the signals over several pulses from one and the same detector, as disclosed in claim 28. This improves the S/N ratio, and may, e.g., be relevant in measurements of many pollutant gases in ambient air indoors and outdoors, whose relative abundances are a question of millionths (ppm) or less.
- Carbon monoxide is a colourless and odourless gas, which accompanies incomplete combustion in gas ovens as well as in fires. For instance, fire casulties normally die from carbon monoxide poisoning long before the fire is fully developed. Measurement of carbon monoxide thus may lead to improved warnings of fires as well as poisonous gas, and it is recognized in those trades that such needs do exist. Because of their complexity and price, however, IR sensors have not so far been applied to said purposes in any large scale, while other kinds of gas sensors have not been regarded as sufficiently reliable. The actual gas densities that must be measured and warned of, are, in both cases, a matter of the order of 100 ppm. This is within reach of the present sensors. Claim 29 discloses the detection and warning of carbon monoxide for the said purposes as a relevant and timely application. The challenge shall be to make the sensors sufficiently inexpensive, so as to compete with existing technology based on quite different technical principles of measurement.
- a sensor may be mounted in front of the mouth orifice, ideally as a stand-alone unit but alternatively also as a component in some larger instrumentation comprising hoses and other devices.
- measurements on the inspiration air also provides a zero level reference once per respiration cycle in relation to gas exhaled from the lungs.
- the time between two consecutive inspirations or exhalations may provide a simple measure for the respiration frequency, which may in many circumstances be useful to assist in calculating the exhaled volume of gas, since the IR measurement itself measures only the gas density.
- An interesting variant of the said application thus would be a sensor to be used for athletes (and animals!) to monitor the carbon dioxide exhaled during exercise, with the option of optimizing and improving the efficiency of techniques and energy expenditure.
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Abstract
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Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA002336826A CA2336826A1 (en) | 1998-07-17 | 1999-07-19 | Infrared radiation source and its application for gas measurement |
US09/743,866 US6540690B1 (en) | 1998-07-17 | 1999-07-19 | Infrared radiation source and its application for gas measurement |
JP2000560421A JP2002520611A (en) | 1998-07-17 | 1999-07-19 | Infrared radiation source and its application for gas measurement |
AU57650/99A AU748350B2 (en) | 1998-07-17 | 1999-07-19 | Infrared radiation source and its application for gas measurement |
EP99944933A EP1101082A2 (en) | 1998-07-17 | 1999-07-19 | Infrared radiation source and its application for gas measurement |
NO20010102A NO20010102D0 (en) | 1998-07-17 | 2001-01-08 | Infrared radiation source and its use for gas measurement |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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NO19983334 | 1998-07-17 | ||
NO983334A NO983334L (en) | 1998-07-17 | 1998-07-17 | Method of measuring gas |
NO19983335 | 1998-07-17 | ||
NO19983335A NO312860B1 (en) | 1998-07-17 | 1998-07-17 | Method for forming and fastening a thin, pulse-heated body |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
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US09/743,866 A-371-Of-International US6540690B1 (en) | 1998-07-17 | 1999-07-19 | Infrared radiation source and its application for gas measurement |
US10/355,008 Division US6652468B2 (en) | 1998-07-17 | 2003-01-31 | Infrared radiation source and its application for gas measurement |
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WO2000004351A2 true WO2000004351A2 (en) | 2000-01-27 |
WO2000004351A3 WO2000004351A3 (en) | 2000-04-20 |
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PCT/NO1999/000240 WO2000004351A2 (en) | 1998-07-17 | 1999-07-19 | Infrared radiation source and its application for gas measurement |
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AU (1) | AU748350B2 (en) |
WO (1) | WO2000004351A2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004068120A1 (en) * | 2003-01-22 | 2004-08-12 | Robert Bosch Gmbh | Infra-red source and gas sensor |
CN110214267A (en) * | 2016-11-18 | 2019-09-06 | 法国电力公司 | For estimating the mancarried device and method of Polymer Parameters |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4620104A (en) * | 1982-02-22 | 1986-10-28 | Nordal Per Erik | Infrared radiation source arrangement |
US4644141A (en) * | 1984-10-12 | 1987-02-17 | Dragerwerk Ag | Infrared radiator |
US4859859A (en) * | 1986-12-04 | 1989-08-22 | Cascadia Technology Corporation | Gas analyzers |
US5220173A (en) * | 1989-05-26 | 1993-06-15 | Kanstad Teknologi A.S. | Pulsating infrared radiation source |
US5324951A (en) * | 1990-09-18 | 1994-06-28 | Servomex (Uk) Ltd. | Infra-red source |
US5369277A (en) * | 1990-05-23 | 1994-11-29 | Ntc Technology, Inc. | Infrared source |
US5567951A (en) * | 1994-06-01 | 1996-10-22 | Heraeus Noblelight Gmbh | Radiating apparatus |
WO1997004623A1 (en) * | 1995-07-21 | 1997-02-06 | Kanstad Teknologi A.S | Efficient metallic infrared radiation source |
WO1997009593A1 (en) * | 1995-09-08 | 1997-03-13 | Patinor A/S | Infrared emitter and methods for fabricating the same |
EP0859536A1 (en) * | 1997-02-15 | 1998-08-19 | Cerberus Ag | Infrared radiator and its application |
US5838016A (en) * | 1995-08-03 | 1998-11-17 | Johnson; Edward A. | Infrared radiation filament and method of manufacture |
-
1999
- 1999-07-19 WO PCT/NO1999/000240 patent/WO2000004351A2/en not_active Application Discontinuation
- 1999-07-19 AU AU57650/99A patent/AU748350B2/en not_active Ceased
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4620104A (en) * | 1982-02-22 | 1986-10-28 | Nordal Per Erik | Infrared radiation source arrangement |
US4644141A (en) * | 1984-10-12 | 1987-02-17 | Dragerwerk Ag | Infrared radiator |
US4859859A (en) * | 1986-12-04 | 1989-08-22 | Cascadia Technology Corporation | Gas analyzers |
US5220173A (en) * | 1989-05-26 | 1993-06-15 | Kanstad Teknologi A.S. | Pulsating infrared radiation source |
US5369277A (en) * | 1990-05-23 | 1994-11-29 | Ntc Technology, Inc. | Infrared source |
US5324951A (en) * | 1990-09-18 | 1994-06-28 | Servomex (Uk) Ltd. | Infra-red source |
US5567951A (en) * | 1994-06-01 | 1996-10-22 | Heraeus Noblelight Gmbh | Radiating apparatus |
WO1997004623A1 (en) * | 1995-07-21 | 1997-02-06 | Kanstad Teknologi A.S | Efficient metallic infrared radiation source |
US5838016A (en) * | 1995-08-03 | 1998-11-17 | Johnson; Edward A. | Infrared radiation filament and method of manufacture |
WO1997009593A1 (en) * | 1995-09-08 | 1997-03-13 | Patinor A/S | Infrared emitter and methods for fabricating the same |
EP0859536A1 (en) * | 1997-02-15 | 1998-08-19 | Cerberus Ag | Infrared radiator and its application |
Non-Patent Citations (1)
Title |
---|
LAINE D.C., AL-JOURANI M.M., CARPENTER C., SEDGBEER M.: 'Pulsed wideband IR thermal source' OPTOELECTRONICS, IEE PROCEEDINGS vol. 144, no. 5, 01 October 1997, pages 315 - 322, XP006008871 * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004068120A1 (en) * | 2003-01-22 | 2004-08-12 | Robert Bosch Gmbh | Infra-red source and gas sensor |
US7728314B2 (en) | 2003-01-22 | 2010-06-01 | Robert Bosch Gmbh | Infra-red source and gas sensor |
CN110214267A (en) * | 2016-11-18 | 2019-09-06 | 法国电力公司 | For estimating the mancarried device and method of Polymer Parameters |
CN110214267B (en) * | 2016-11-18 | 2023-01-10 | 法国电力公司 | Portable device and method for estimating polymer parameters |
Also Published As
Publication number | Publication date |
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AU5765099A (en) | 2000-02-07 |
AU748350B2 (en) | 2002-06-06 |
WO2000004351A3 (en) | 2000-04-20 |
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