|Publication number||US3699342 A|
|Publication date||Oct 17, 1972|
|Filing date||Aug 13, 1970|
|Priority date||Apr 27, 1970|
|Also published as||USRE28417|
|Publication number||US 3699342 A, US 3699342A, US-A-3699342, US3699342 A, US3699342A|
|Inventors||Cornell Richard Charles, Jenkins Anthony|
|Original Assignee||Analytical Instr Ltd|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (2), Referenced by (4), Classifications (12)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent Jenkins et al.
[ 51 Oct. 17,1972
 METHOD AND APPARATUS FOR 3,545,931 12/1970 McKinley, Jr. ..55/16 DETECTING TRACER GAS  Inventors: Anthony Jenkins; Rlchard Charles Primary Examiner-Archie Borchelt Come, both f Fowlmere, near Attorney-Woodhams, Blanchard & Flynn Royston, England I  Assignee: Analytical Instruments Limited,  ABSTRACT Royston, England A method and apparatus for detecting the presence of  Filed l31970 an halogenated tracer gas, which is an electron absorber, in an environment which is itself, or comprises PP 63,571 as a constituent, an electron absorber. The apparatus comprises an electron capture detector and the en- 30 Foreign Application p i i D ta vironment to be sampled is first drawn through a membrane which has a greater permeability to the April qreat Bmam "20l80/70 tracergas than the remainder of the environment be- [521 U S 250/83 6 FT 55/16 250/43 5 FC fore being carried into the detector by a carrier gas. 511 IQL CLIIIIIIIII .3 .....G0lt 1/18 This results in a diminutim the cncemratin  Field of Search 250/83 6 F1435 PC, 435 any electron capture agents present in the environ- 7 ;23 232 54;55 1 71 15 ment and which if drawn into the detector could swamp the effect of the tracer gas.  Reigrences Cited 3 Claims, 2 Drawing Figures UNITED STATES PATENTS 3,361,908 1/1968 Petitjean et al. ....250/83.6 FT
' 1O 14 12' 1g I i l EXHAUST 20 i l gas system. In two known methods thetracer gas has been helium, which is detectable by a mass spectrometer and freon which is detectable by a halogen detector. The mass spectrometer is both bulky and expensive.
The halogen detectors are not sufficiently sensitive for a number of applications.
detector for detecting the presence of the tracer gas.
An-electron capture detector'generally comprises an ionization chamber containing a B particle emitter, such as tritium, as the primary source of ionizing radia tion. Upon entry into the chamber of a carrier gas such as nitrogen possessing no affinity for electrons, recombination of positive ions and free electrons formed by the. ionizing radiation is unlikely to take place because of the free electrons high mobility. Thus by applying a small potential across the chamber all ions formed by the ionizing radiation can be collected. When the carri-.
er gas contains a compound having an affinity for electrons, negative ion formation occurs which is accompanied by an observed decrease in current.
The present invention seeks to provide a method and apparatus which can be used to monitor atmospheric air or other gas samples for the presence and concentration of sulphur hexafluoride aNd other halogenated tracer gases. Oxygen itself is capable of electron capture and it could therefore saturate the detector.
According to one aspect of the present invention a method of detecting and monitoring the presence of halogenated tracer gas in a gas supply having as a major constituent thereof an electron capture material comprises selectively isolating said tracer gas from the remainder of the supply by diffusion through a membrane having a greater permeability to said tracer gas than to the remainder of thesupply, and thereafter conveying the tracer gas into an electron capture detector by means of a gas stream substantially inert to electron capture.
According to another aspect of the present invention, an apparatus for detecting an monitoring the presence of halogenated tracer gas supply comprises a probe carrying a membrane having a greater permeability to said halogenated tracer gas or gases than the remainder of the gas supply, means for conveying a carrier gas to the side of the membrane remote from the gas supply and an electron capture detector to receive said carrier gas containing the halogenated tracer gas whereby to detect the latter.
When the halogenated tracer gas is present in the atmosphere it is necessary to separate the tracer gas from the oxygen of the atmosphere prior to introduction into the detector. Oxygen is itself an electron absorber and its presence would saturate the detector and effectively blanket the presence of the tracer gas. Sufficient amount of the tracer gas must be introduced into the detector to obtain a useful response of the detector and it is therefore necessary to separate the tracer gas from the atmospheric oxygen prior to its introduction into the detector.
This is achieved by separating the detector from the atmosphere or other gas supply containing a preponderance of an electron capture material in addition to the electron capture tracer gas by means of a membrane. The tracer gas can pass through the membrane and is then swept into the detector by a stream of inert gas i.e. inert to electron capture. A suitable carrier gas is nitrogen.
A suitable membrane is formed from a silastomer.
The invention will be described further by way of example with reference to the accompanying drawings in which:
FIG. 1 is a diagrammatic representation of an apparatus according to the invention, and
FIG. 2 shows a modification of part of the apparatus in which a sampling probe is contained in an outer sheath.
A sampling probe 10 for introducing a gas to be analyzed into an electron capture detector is closed at one end by a membrane 12. The membrane is preferably formed from a silastomer as this has a permeability to some halogenated tracer gases which is of the order of ten times greater than that to oxygen. The opposite end of the probe is connected through a line 14 controlled by a valve 16 to a nitrogen supply, the nitrogen serving as a carrier gas to convey the gas to be analyzed into the electron capture detector 18 by way of a line 20. The line 20 commences adjacent the membrane 12. An amplifier 22 and a meter 24 are connected to the detector. When the gas to be analyzed contains tracer gas and is introduced into the detector this results in a change in the ionization current which charge is'indicative of the concentration of tracer gas in the nitrogen carrier gas stream and is noted on the meter 24.
The term silastomer refers to a thin film or sheet of silicone rubber.
In FIG. 2, the sampling probe 10 is contained within an outer sheath 30. The end of the sheath 30 adjacent the membrane 12 is open to the atmosphere while the other end of the sheath communicates through line 32 with a suction means, for example an air pump (not shown). The pump draws air or gas to be sampled into the sheath and into contact with the membrane. Furthermore, as shown in FIG. 2, the exhaust from the detector 18 can be connected to the suction line 32. This provides a convenient method of determining flow from the detector. The draft created by the suction makes the probe less directionally sensitive and it can pick up a tracer gas at greater distances from a leak than the apparatus of FIG. 1.
The apparatus can be used for detecting leaks in a gas system having a halogenated tracer gas. Examples of tracer agents are sulphur hexafluoride SP and Freons (Registered Trade Mark) such as dichloroditluoromethane CC1 F and bromochlorodifluoromethane CBrC1F One particular use of the apparatus lies in the detection of leaks in containers such as aerosols. On account of its high sensitivity the apparatus can detect the presence of a very small leak and can be used to monitor such containers prior to their dispatch to consumers. The apparatus is compact and readily transportable.
The apparatus is also sensitive to the presence of nitrmcompounds, such as nitroglycerine. Thus it is envisaged that the apparatus can find use as a detector for of a gas stream substantially inert to electron capture.
2. An apparatus for detecting and monitoring the presence of an electron capture halogenated tracer gas in a gas supply which is itself, or includes as a con-' stituent, an electron capture material, the apparatus comprising a probe, a membrane at an end of said probe in which the membrane comprises a silastomer having a greater permeability to the halogenated tracer gas than the remainder of the gas supply, means for conveying a carrier gas to the side of the membrane remote from the gas supply and an electron capture detector to receive the carrier gas and tracer gas.
3. An apparatus. according to claim 2, including an outer sheath surrounding the probe and open to the atmosphere at one end, suction means being connected to the other end of the sheath whereby to draw in a sample into the vicinity of the membrane.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3361908 *||Jan 3, 1964||Jan 2, 1968||Barber Colman Co||Method and apparatus for electron attachment detection|
|US3545931 *||Aug 28, 1968||Dec 8, 1970||Monsanto Co||Ammonia analysis system|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US4304752 *||Mar 23, 1979||Dec 8, 1981||Anthony Jenkins||Detection of tracer materials in the atmosphere|
|US4793830 *||Dec 28, 1987||Dec 27, 1988||Murphy Milton K||Process for producing high quality gas for instrumentation application using gas separation membranes|
|US20100251803 *||Jun 22, 2010||Oct 7, 2010||E. I. Du Pont De Nemours And Company||Detectable refrigerant compositions and uses thereof|
|EP0046699A2 *||Jul 22, 1981||Mar 3, 1982||The Bendix Corporation||Ion mobility detector provided with a membrane interface|
|U.S. Classification||250/302, 95/48, 250/389, 250/303, 96/4, 95/25|
|International Classification||G01N27/64, G01N15/06|
|Cooperative Classification||G01N15/0618, G01N27/64|
|European Classification||G01N27/64, G01N15/06A3|