IL127206A - Method of explosives detection - Google Patents

Method of explosives detection

Info

Publication number: IL127206A
Authority: IL; Israel
Prior art keywords: chamber; sample; gas; light; detection
Prior art date: 1996-06-12

Application number

IL12720697A

Other languages

English (en)

Other versions

IL127206A0 (en

Original Assignee

Sec Dep For Defence Defence Ev

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.)

1996-06-12

Filing date

1997-06-10

Publication date

2001-10-31

1997-06-10 Application filed by Sec Dep For Defence Defence Ev filed Critical Sec Dep For Defence Defence Ev

1999-09-22 Publication of IL127206A0 publication Critical patent/IL127206A0/xx

2001-10-31 Publication of IL127206A publication Critical patent/IL127206A/en

Links

238000000034 method Methods 0.000 title claims abstract description 34
238000001514 detection method Methods 0.000 title claims abstract description 19
239000002360 explosive Substances 0.000 title claims description 13
239000000463 material Substances 0.000 claims abstract description 21
239000007789 gas Substances 0.000 claims description 15
238000010438 heat treatment Methods 0.000 claims description 13
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 12
238000004817 gas chromatography Methods 0.000 claims description 10
239000010453 quartz Substances 0.000 claims description 10
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 9
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 6
239000001307 helium Substances 0.000 claims description 5
229910052734 helium Inorganic materials 0.000 claims description 5
SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 claims description 5
230000005855 radiation Effects 0.000 claims description 5
239000011261 inert gas Substances 0.000 claims description 4
229910052757 nitrogen Inorganic materials 0.000 claims description 4
229910052786 argon Inorganic materials 0.000 claims description 3
150000002978 peroxides Chemical class 0.000 claims description 3
230000000063 preceeding effect Effects 0.000 claims 2
239000011248 coating agent Substances 0.000 claims 1
238000000576 coating method Methods 0.000 claims 1
239000000126 substance Substances 0.000 description 20
239000000523 sample Substances 0.000 description 17
239000000203 mixture Substances 0.000 description 14
239000012159 carrier gas Substances 0.000 description 10
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 9
238000006243 chemical reaction Methods 0.000 description 9
SNIOPGDIGTZGOP-UHFFFAOYSA-N Nitroglycerin Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 description 8
TZRXHJWUDPFEEY-UHFFFAOYSA-N Pentaerythritol Tetranitrate Chemical compound [O-][N+](=O)OCC(CO[N+]([O-])=O)(CO[N+]([O-])=O)CO[N+]([O-])=O TZRXHJWUDPFEEY-UHFFFAOYSA-N 0.000 description 8
229960003711 glyceryl trinitrate Drugs 0.000 description 8
SPSSULHKWOKEEL-UHFFFAOYSA-N 2,4,6-trinitrotoluene Chemical compound CC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O SPSSULHKWOKEEL-UHFFFAOYSA-N 0.000 description 7
239000000015 trinitrotoluene Substances 0.000 description 7
230000004044 response Effects 0.000 description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
238000002347 injection Methods 0.000 description 5
239000007924 injection Substances 0.000 description 5
-1 alkyl nitrate Chemical compound 0.000 description 4
UQXKXGWGFRWILX-UHFFFAOYSA-N ethylene glycol dinitrate Chemical compound O=N(=O)OCCON(=O)=O UQXKXGWGFRWILX-UHFFFAOYSA-N 0.000 description 4
230000004043 responsiveness Effects 0.000 description 4
239000000243 solution Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
238000001228 spectrum Methods 0.000 description 4
NKRVGWFEFKCZAP-UHFFFAOYSA-N 2-ethylhexyl nitrate Chemical compound CCCCC(CC)CO[N+]([O-])=O NKRVGWFEFKCZAP-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
230000000694 effects Effects 0.000 description 3
SNFOERUNNSHUGP-ZXZARUISSA-N erythrityl tetranitrate Chemical compound [O-][N+](=O)OC[C@@H](O[N+]([O-])=O)[C@@H](O[N+]([O-])=O)CO[N+]([O-])=O SNFOERUNNSHUGP-ZXZARUISSA-N 0.000 description 3
IDNUEBSJWINEMI-UHFFFAOYSA-N ethyl nitrate Chemical compound CCO[N+]([O-])=O IDNUEBSJWINEMI-UHFFFAOYSA-N 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
230000003287 optical effect Effects 0.000 description 3
GFVHBTOOPNJKLV-UHFFFAOYSA-N 1,2-dinitroglycerol Chemical compound [O-][N+](=O)OC(CO)CO[N+]([O-])=O GFVHBTOOPNJKLV-UHFFFAOYSA-N 0.000 description 2
ASIGVDLTBLZXNC-UHFFFAOYSA-N 1,3-dinitroglycerol Chemical compound [O-][N+](=O)OCC(O)CO[N+]([O-])=O ASIGVDLTBLZXNC-UHFFFAOYSA-N 0.000 description 2
ZTLXICJMNFREPA-UHFFFAOYSA-N 3,3,6,6,9,9-hexamethyl-1,2,4,5,7,8-hexaoxonane Chemical compound CC1(C)OOC(C)(C)OOC(C)(C)OO1 ZTLXICJMNFREPA-UHFFFAOYSA-N 0.000 description 2
SJQITXILEOCXGI-UHFFFAOYSA-N 3,3,6,6-tetramethyl-1,2,4,5-tetraoxane Chemical compound CC1(C)OOC(C)(C)OO1 SJQITXILEOCXGI-UHFFFAOYSA-N 0.000 description 2
CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
239000000470 constituent Substances 0.000 description 2
230000001419 dependent effect Effects 0.000 description 2
LYAGTVMJGHTIDH-UHFFFAOYSA-N diethylene glycol dinitrate Chemical compound [O-][N+](=O)OCCOCCO[N+]([O-])=O LYAGTVMJGHTIDH-UHFFFAOYSA-N 0.000 description 2
239000010408 film Substances 0.000 description 2
238000001031 gas chromatography-thermal energy analyser Methods 0.000 description 2
DGMJZELBSFOPHH-KVTDHHQDSA-N mannite hexanitrate Chemical compound [O-][N+](=O)OC[C@@H](O[N+]([O-])=O)[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)CO[N+]([O-])=O DGMJZELBSFOPHH-KVTDHHQDSA-N 0.000 description 2
229960001765 mannitol hexanitrate Drugs 0.000 description 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
QAXAHXNXXIWQIZ-UHFFFAOYSA-N n,n-diethylnitramide Chemical compound CCN(CC)[N+]([O-])=O QAXAHXNXXIWQIZ-UHFFFAOYSA-N 0.000 description 2
229910001120 nichrome Inorganic materials 0.000 description 2
239000000376 reactant Substances 0.000 description 2
230000035945 sensitivity Effects 0.000 description 2
238000000926 separation method Methods 0.000 description 2
AGCQZYRSTIRJFM-UHFFFAOYSA-N triethylene glycol dinitrate Chemical compound [O-][N+](=O)OCCOCCOCCO[N+]([O-])=O AGCQZYRSTIRJFM-UHFFFAOYSA-N 0.000 description 2
IPPYBNCEPZCLNI-UHFFFAOYSA-N trimethylolethane trinitrate Chemical compound [O-][N+](=O)OCC(C)(CO[N+]([O-])=O)CO[N+]([O-])=O IPPYBNCEPZCLNI-UHFFFAOYSA-N 0.000 description 2
BPUGKGGCLABYPO-UHFFFAOYSA-N (2-ethyl-3-nitrooxyhexyl) nitrate Chemical compound CCCC(O[N+]([O-])=O)C(CC)CO[N+]([O-])=O BPUGKGGCLABYPO-UHFFFAOYSA-N 0.000 description 1
POCJOGNVFHPZNS-ZJUUUORDSA-N (6S,7R)-2-azaspiro[5.5]undecan-7-ol Chemical compound O[C@@H]1CCCC[C@]11CNCCC1 POCJOGNVFHPZNS-ZJUUUORDSA-N 0.000 description 1
RDLIBIDNLZPAQD-UHFFFAOYSA-N 1,2,4-butanetriol trinitrate Chemical compound [O-][N+](=O)OCCC(O[N+]([O-])=O)CO[N+]([O-])=O RDLIBIDNLZPAQD-UHFFFAOYSA-N 0.000 description 1
HXWLJBVVXXBZCM-UHFFFAOYSA-N 2,3-dihydroxypropyl nitrate Chemical compound OCC(O)CO[N+]([O-])=O HXWLJBVVXXBZCM-UHFFFAOYSA-N 0.000 description 1
UYXOJHWUUPHPRF-UHFFFAOYSA-N 2-nitrooxypentan-3-yl nitrate Chemical compound [O-][N+](=O)OC(CC)C(C)O[N+]([O-])=O UYXOJHWUUPHPRF-UHFFFAOYSA-N 0.000 description 1
RVDDYBGRQLZMSB-UHFFFAOYSA-N 3-nitrooxybutan-2-yl nitrate Chemical compound [O-][N+](=O)OC(C)C(C)O[N+]([O-])=O RVDDYBGRQLZMSB-UHFFFAOYSA-N 0.000 description 1
QPJRYGFPFMEBTR-UHFFFAOYSA-N 3-nitropentan-2-yl nitrate Chemical compound CCC([N+]([O-])=O)C(C)O[N+]([O-])=O QPJRYGFPFMEBTR-UHFFFAOYSA-N 0.000 description 1
DGFBULNMARLFTH-UHFFFAOYSA-N 4-nitrooxybutan-2-yl nitrate Chemical compound [O-][N+](=O)OC(C)CCO[N+]([O-])=O DGFBULNMARLFTH-UHFFFAOYSA-N 0.000 description 1
RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
229910002651 NO3 Inorganic materials 0.000 description 1
101100217524 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) apg-1 gene Proteins 0.000 description 1
BSPUVYFGURDFHE-UHFFFAOYSA-N Nitramine Natural products CC1C(O)CCC2CCCNC12 BSPUVYFGURDFHE-UHFFFAOYSA-N 0.000 description 1
239000004642 Polyimide Substances 0.000 description 1
229910045601 alloy Inorganic materials 0.000 description 1
239000000956 alloy Substances 0.000 description 1
239000004411 aluminium Substances 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
230000003466 anti-cipated effect Effects 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
230000005540 biological transmission Effects 0.000 description 1
239000004568 cement Substances 0.000 description 1
239000000919 ceramic Substances 0.000 description 1
238000013375 chromatographic separation Methods 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
229910001873 dinitrogen Inorganic materials 0.000 description 1
238000000295 emission spectrum Methods 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000008246 gaseous mixture Substances 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
POCJOGNVFHPZNS-UHFFFAOYSA-N isonitramine Natural products OC1CCCCC11CNCCC1 POCJOGNVFHPZNS-UHFFFAOYSA-N 0.000 description 1
238000005259 measurement Methods 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
229910052754 neon Inorganic materials 0.000 description 1
GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 description 1
YHSOMIDYWSMROG-UHFFFAOYSA-N nitric acid;propane-1,2-diol Chemical compound O[N+]([O-])=O.CC(O)CO YHSOMIDYWSMROG-UHFFFAOYSA-N 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
229920001721 polyimide Polymers 0.000 description 1
239000003380 propellant Substances 0.000 description 1
238000005086 pumping Methods 0.000 description 1
239000005297 pyrex Substances 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
150000003384 small molecules Chemical class 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
239000010409 thin film Substances 0.000 description 1
238000002834 transmittance Methods 0.000 description 1

Classifications

- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/0004—Gaseous mixtures, e.g. polluted air
- G01N33/0009—General constructional details of gas analysers, e.g. portable test equipment
- G01N33/0027—General constructional details of gas analysers, e.g. portable test equipment concerning the detector
- G01N33/0036—General constructional details of gas analysers, e.g. portable test equipment concerning the detector specially adapted to detect a particular component
- G01N33/0057—Warfare agents or explosives
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T436/00—Chemistry: analytical and immunological testing
- Y10T436/17—Nitrogen containing
- Y10T436/173076—Nitrite or nitrate
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T436/00—Chemistry: analytical and immunological testing
- Y10T436/20—Oxygen containing
- Y10T436/206664—Ozone or peroxide

Landscapes

Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Health & Medical Sciences (AREA)
Analytical Chemistry (AREA)
Food Science & Technology (AREA)
Medicinal Chemistry (AREA)
Physics & Mathematics (AREA)
Combustion & Propulsion (AREA)
Biochemistry (AREA)
General Health & Medical Sciences (AREA)
General Physics & Mathematics (AREA)
Immunology (AREA)
Pathology (AREA)
Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
Sampling And Sample Adjustment (AREA)

IL12720697A 1996-06-12 1997-06-10 Method of explosives detection IL127206A (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB9612241A GB2314156A (en)	1996-06-12	1996-06-12	Explosives detection
PCT/GB1997/001555 WO1997047958A1 (fr)	1996-06-12	1997-06-10	Procede de detection d'explosifs

Publications (2)

Publication Number	Publication Date
IL127206A0 IL127206A0 (en)	1999-09-22
IL127206A true IL127206A (en)	2001-10-31

Family

ID=10795145

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL12720697A IL127206A (en)	1996-06-12	1997-06-10	Method of explosives detection

Country Status (9)

Country	Link
US (1)	US6245576B1 (fr)
EP (1)	EP0904531B1 (fr)
JP (1)	JP2000512755A (fr)
CA (1)	CA2257940C (fr)
DE (1)	DE69715843T2 (fr)
GB (1)	GB2314156A (fr)
IL (1)	IL127206A (fr)
WO (1)	WO1997047958A1 (fr)
ZA (1)	ZA975179B (fr)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB2328740B (en) *	1996-06-12	2000-06-07	Secr Defence	Method of explosives detection
IL123451A (en)	1998-02-25	2003-07-06	Ehud Keinan	Method and kit for the detection of peroxide-based explosives
US6558626B1 (en)	2000-10-17	2003-05-06	Nomadics, Inc.	Vapor sensing instrument for ultra trace chemical detection
US6984524B2 (en) *	2002-09-12	2006-01-10	Control Screening, Llc	Chemiluminescent detection of explosives, narcotics, and other chemical substances
US7294306B2 (en)	2003-06-30	2007-11-13	The Regents Of The University Of California	Inspection tester for explosives
US7867445B1 (en) *	2003-06-30	2011-01-11	Lawrence Livermore National Security, Llc	Explosives tester
US7745227B2 (en) *	2003-08-12	2010-06-29	Lawrence Livermore National Security, Llc	System for analysis of explosives
EP1844321A1 (fr) *	2005-01-25	2007-10-17	System Two Pty Ltd	Dispositif de test
US20090113982A1 (en) *	2005-02-25	2009-05-07	Robert Hodyss	Multi-dimensional explosive detector
US20110151575A1 (en) *	2005-07-27	2011-06-23	L-3 Communications Cyterra Corporation	Energetic Material Detector
US8292496B1 (en) *	2005-07-27	2012-10-23	L-3 Communications Cyterra Corporation	Energetic material detector
AU2006345002B2 (en) *	2005-07-27	2012-02-02	L-3 Communications Cyterra Corporation	Energetic material detector
US20070111321A1 (en) *	2005-08-31	2007-05-17	Nomadics, Inc.	Detection of explosives and other species
US7799573B2 (en)	2005-08-31	2010-09-21	Normadics, Inc.	Detection of explosives and other species
WO2008080100A1 (fr) *	2006-12-22	2008-07-03	L-3 Communications Cyterra Corporation	Détecteur de matière énergétique
WO2008121124A1 (fr)	2007-03-19	2008-10-09	Nomadics, Inc.	Détecteur de peroxyde d'hydrogène et procédés
DE102007062281A1 (de) *	2007-12-21	2009-06-25	Bayer Materialscience Ag	Verfahren und Vorrichtung zur Prüfung der Brandgefahr eines Werkstoffes
CN110296975B (zh) *	2019-05-29	2021-11-09	北京理工大学	含能材料宏观参数快速检测光谱系统
DE102020112570A1 (de) *	2020-05-08	2021-11-11	Analytik Jena Gmbh	Vorrichtung zur Chemolumineszenzanalyse

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3996002A (en) *	1973-02-05	1976-12-07	Thermo Electron Corporation	Method and apparatus for measuring the n-nitroso compound content of a sample
GB1511286A (en) *	1974-09-20	1978-05-17	Petroleo Brasileiro Sa	Process for the determination of chemical compounds by chemiluminescence with ozone
US4193963A (en) *	1974-09-20	1980-03-18	Petroleo Brasileiro S.A.-Petrobras	Apparatus for the determination of chemical compounds by chemiluminescence with ozone
GB2016679A (en) *	1978-03-14	1979-09-26	Boc Ltd	Chemiluminescence Gas Analysing Apparatus
US4717675A (en) *	1984-08-03	1988-01-05	Sievers Research, Inc.	Method for selective conversion of organic compounds and detecting same by gas chromotography and chemiluminescence detection
US5092156A (en) *	1987-07-08	1992-03-03	Thermedics Inc.	Vapor collector/desorber with tube bundle and metal foil
US5092220A (en) *	1987-07-08	1992-03-03	Thermedics Inc.	Nitric oxide detection with hydrogen and ozone
US5094815A (en) *	1988-05-18	1992-03-10	Cornell Research Foundation, Inc.	Photolytic interface for HPLC-chemiluminescence detection of non volatile N-nitroso compounds
US5459076A (en) *	1992-04-22	1995-10-17	Brigham And Women's Hospital	Method for detecting nitric oxide, nitrosonium equivalents, S-nitrosothiols and S-nitroso-proteins in biological systems

1996
- 1996-06-12 GB GB9612241A patent/GB2314156A/en not_active Withdrawn
1997
- 1997-06-10 IL IL12720697A patent/IL127206A/en not_active IP Right Cessation
- 1997-06-10 EP EP97925181A patent/EP0904531B1/fr not_active Expired - Lifetime
- 1997-06-10 CA CA002257940A patent/CA2257940C/fr not_active Expired - Fee Related
- 1997-06-10 WO PCT/GB1997/001555 patent/WO1997047958A1/fr not_active Ceased
- 1997-06-10 DE DE69715843T patent/DE69715843T2/de not_active Expired - Lifetime
- 1997-06-10 US US09/180,953 patent/US6245576B1/en not_active Expired - Fee Related
- 1997-06-10 JP JP10501346A patent/JP2000512755A/ja active Pending
- 1997-06-11 ZA ZA9705179A patent/ZA975179B/xx unknown

Also Published As

Publication number	Publication date
GB2314156A (en)	1997-12-17
GB9612241D0 (en)	1996-08-14
ZA975179B (en)	1998-01-05
EP0904531B1 (fr)	2002-09-25
JP2000512755A (ja)	2000-09-26
US6245576B1 (en)	2001-06-12
WO1997047958A1 (fr)	1997-12-18
DE69715843T2 (de)	2003-05-28
CA2257940C (fr)	2009-11-03
IL127206A0 (en)	1999-09-22
CA2257940A1 (fr)	1997-12-18
DE69715843D1 (de)	2002-10-31
EP0904531A1 (fr)	1999-03-31

Legal Events

Date	Code	Title
2003-07-31	KB	Patent renewed
2007-09-20	KB	Patent renewed
2016-01-31	MM9K	Patent not in force due to non-payment of renewal fees

Publication	Publication Date	Title
EP0904531B1 (fr)	2002-09-25	Procede de detection d'explosifs
Chong et al.	1987	Inductively coupled plasma-mass spectrometry for elemental analysis and isotope ratio determinations in individual organic compounds separated by gas chromatography
US8174691B1 (en)	2012-05-08	Detection of a component of interest with an ultraviolet laser and method of using the same
US5092219A (en)	1992-03-03	Selective decomposition of nitrite esters and nitramines
US5621522A (en)	1997-04-15	Fiber optic probe for determination of trace levels of organic pollutants using Raman spectroscopy
US5108705A (en)	1992-04-28	Vapor detection with high speed gas chromatography
WO1991008466A1 (fr)	1991-06-13	Detection selective de vapeurs
US5092220A (en)	1992-03-03	Nitric oxide detection with hydrogen and ozone
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