JP2022509550A - 揮発性有機化合物を収集するための装置 - Google Patents
揮発性有機化合物を収集するための装置 Download PDFInfo
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- JP2022509550A JP2022509550A JP2021549924A JP2021549924A JP2022509550A JP 2022509550 A JP2022509550 A JP 2022509550A JP 2021549924 A JP2021549924 A JP 2021549924A JP 2021549924 A JP2021549924 A JP 2021549924A JP 2022509550 A JP2022509550 A JP 2022509550A
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- JP
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- Prior art keywords
- methyl
- acid
- volatile organic
- support
- dimethyl
- 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.)
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- 239000012855 volatile organic compound Substances 0.000 title claims abstract description 51
- 239000003205 fragrance Substances 0.000 claims abstract description 21
- 238000000034 method Methods 0.000 claims abstract description 18
- -1 polydimethylsiloxane Polymers 0.000 claims description 86
- 238000001179 sorption measurement Methods 0.000 claims description 50
- 238000004817 gas chromatography Methods 0.000 claims description 15
- 238000003795 desorption Methods 0.000 claims description 13
- 238000010521 absorption reaction Methods 0.000 claims description 6
- 239000006229 carbon black Substances 0.000 claims description 4
- 239000002808 molecular sieve Substances 0.000 claims description 4
- 229920000620 organic polymer Polymers 0.000 claims description 4
- 230000003134 recirculating effect Effects 0.000 claims description 4
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 claims description 4
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 3
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 3
- 238000007789 sealing Methods 0.000 claims description 3
- 229920000858 Cyclodextrin Polymers 0.000 claims description 2
- WVVOBOZHTQJXPB-UHFFFAOYSA-N N-anilino-N-nitronitramide Chemical compound [N+](=O)([O-])N(NC1=CC=CC=C1)[N+](=O)[O-] WVVOBOZHTQJXPB-UHFFFAOYSA-N 0.000 claims description 2
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 claims description 2
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical group O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 claims description 2
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 claims description 2
- 238000010586 diagram Methods 0.000 abstract 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 75
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 24
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 21
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 18
- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 18
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 16
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 14
- 238000004519 manufacturing process Methods 0.000 description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 12
- DMEGYFMYUHOHGS-UHFFFAOYSA-N cycloheptane Chemical compound C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 12
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 12
- 150000001875 compounds Chemical class 0.000 description 11
- 235000019645 odor Nutrition 0.000 description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 10
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 10
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 10
- YCOZIPAWZNQLMR-UHFFFAOYSA-N pentadecane Chemical compound CCCCCCCCCCCCCCC YCOZIPAWZNQLMR-UHFFFAOYSA-N 0.000 description 10
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 8
- DCTOHCCUXLBQMS-UHFFFAOYSA-N 1-undecene Chemical compound CCCCCCCCCC=C DCTOHCCUXLBQMS-UHFFFAOYSA-N 0.000 description 8
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 8
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 8
- NDJKXXJCMXVBJW-UHFFFAOYSA-N heptadecane Chemical compound CCCCCCCCCCCCCCCCC NDJKXXJCMXVBJW-UHFFFAOYSA-N 0.000 description 8
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 8
- BGHCVCJVXZWKCC-UHFFFAOYSA-N tetradecane Chemical compound CCCCCCCCCCCCCC BGHCVCJVXZWKCC-UHFFFAOYSA-N 0.000 description 8
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 7
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- 150000002148 esters Chemical class 0.000 description 7
- 238000004949 mass spectrometry Methods 0.000 description 7
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 7
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 6
- ZPSJGADGUYYRKE-UHFFFAOYSA-N 2H-pyran-2-one Chemical compound O=C1C=CC=CO1 ZPSJGADGUYYRKE-UHFFFAOYSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 6
- 241000009328 Perro Species 0.000 description 6
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 6
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 6
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 6
- 230000002457 bidirectional effect Effects 0.000 description 6
- AYQPVPFZWIQERS-UHFFFAOYSA-N cis-2-octen-1-ol Natural products CCCCCC=CCO AYQPVPFZWIQERS-UHFFFAOYSA-N 0.000 description 6
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 6
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 6
- BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical compound CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 6
- NUJGJRNETVAIRJ-UHFFFAOYSA-N octanal Chemical compound CCCCCCCC=O NUJGJRNETVAIRJ-UHFFFAOYSA-N 0.000 description 6
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 6
- IIYFAKIEWZDVMP-UHFFFAOYSA-N tridecane Chemical compound CCCCCCCCCCCCC IIYFAKIEWZDVMP-UHFFFAOYSA-N 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- 239000000835 fiber Substances 0.000 description 5
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- 238000002470 solid-phase micro-extraction Methods 0.000 description 5
- UBDIXSAEHLOROW-BUHFOSPRSA-N (E)-7-Tetradecene Chemical compound CCCCCC\C=C\CCCCCC UBDIXSAEHLOROW-BUHFOSPRSA-N 0.000 description 4
- 239000005968 1-Decanol Substances 0.000 description 4
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 4
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 4
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 4
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 4
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 4
- RHDGNLCLDBVESU-UHFFFAOYSA-N but-3-en-4-olide Chemical compound O=C1CC=CO1 RHDGNLCLDBVESU-UHFFFAOYSA-N 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 4
- MLUCVPSAIODCQM-NSCUHMNNSA-N crotonaldehyde Chemical compound C\C=C\C=O MLUCVPSAIODCQM-NSCUHMNNSA-N 0.000 description 4
- MLUCVPSAIODCQM-UHFFFAOYSA-N crotonaldehyde Natural products CC=CC=O MLUCVPSAIODCQM-UHFFFAOYSA-N 0.000 description 4
- PFURGBBHAOXLIO-UHFFFAOYSA-N cyclohexane-1,2-diol Chemical compound OC1CCCCC1O PFURGBBHAOXLIO-UHFFFAOYSA-N 0.000 description 4
- JARKCYVAAOWBJS-UHFFFAOYSA-N hexanal Chemical compound CCCCCC=O JARKCYVAAOWBJS-UHFFFAOYSA-N 0.000 description 4
- 238000009776 industrial production Methods 0.000 description 4
- 238000012423 maintenance Methods 0.000 description 4
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 4
- RZJRJXONCZWCBN-UHFFFAOYSA-N octadecane Chemical compound CCCCCCCCCCCCCCCCCC RZJRJXONCZWCBN-UHFFFAOYSA-N 0.000 description 4
- NMRPBPVERJPACX-UHFFFAOYSA-N octan-3-ol Chemical compound CCCCCC(O)CC NMRPBPVERJPACX-UHFFFAOYSA-N 0.000 description 4
- JYVLIDXNZAXMDK-UHFFFAOYSA-N pentan-2-ol Chemical compound CCCC(C)O JYVLIDXNZAXMDK-UHFFFAOYSA-N 0.000 description 4
- 239000001294 propane Substances 0.000 description 4
- 230000002441 reversible effect Effects 0.000 description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- SZHOJFHSIKHZHA-UHFFFAOYSA-N tridecanoic acid Chemical compound CCCCCCCCCCCCC(O)=O SZHOJFHSIKHZHA-UHFFFAOYSA-N 0.000 description 4
- BSAIUMLZVGUGKX-BQYQJAHWSA-N (E)-non-2-enal Chemical compound CCCCCC\C=C\C=O BSAIUMLZVGUGKX-BQYQJAHWSA-N 0.000 description 3
- GYSCBCSGKXNZRH-UHFFFAOYSA-N 1-benzothiophene-2-carboxamide Chemical compound C1=CC=C2SC(C(=O)N)=CC2=C1 GYSCBCSGKXNZRH-UHFFFAOYSA-N 0.000 description 3
- BSAIUMLZVGUGKX-UHFFFAOYSA-N 2-Nonenal Natural products CCCCCCC=CC=O BSAIUMLZVGUGKX-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 3
- 239000005711 Benzoic acid Substances 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 235000010233 benzoic acid Nutrition 0.000 description 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
- 238000001311 chemical methods and process Methods 0.000 description 3
- 238000011109 contamination Methods 0.000 description 3
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 3
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 3
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 3
- NGAZZOYFWWSOGK-UHFFFAOYSA-N heptan-3-one Chemical compound CCCCC(=O)CC NGAZZOYFWWSOGK-UHFFFAOYSA-N 0.000 description 3
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 3
- PQNFLJBBNBOBRQ-UHFFFAOYSA-N indane Chemical compound C1=CC=C2CCCC2=C1 PQNFLJBBNBOBRQ-UHFFFAOYSA-N 0.000 description 3
- SNWQUNCRDLUDEX-UHFFFAOYSA-N inden-1-one Chemical compound C1=CC=C2C(=O)C=CC2=C1 SNWQUNCRDLUDEX-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 150000004702 methyl esters Chemical class 0.000 description 3
- LABTWGUMFABVFG-UHFFFAOYSA-N methyl propenyl ketone Chemical compound CC=CC(C)=O LABTWGUMFABVFG-UHFFFAOYSA-N 0.000 description 3
- DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- ULSIYEODSMZIPX-UHFFFAOYSA-N phenylethanolamine Chemical compound NCC(O)C1=CC=CC=C1 ULSIYEODSMZIPX-UHFFFAOYSA-N 0.000 description 3
- 235000019260 propionic acid Nutrition 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- KYWIYKKSMDLRDC-UHFFFAOYSA-N undecan-2-one Chemical compound CCCCCCCCCC(C)=O KYWIYKKSMDLRDC-UHFFFAOYSA-N 0.000 description 3
- WQZGKKKJIJFFOK-SVZMEOIVSA-N (+)-Galactose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-SVZMEOIVSA-N 0.000 description 2
- XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- CBXNRMOWVZUZQA-BLWKUPHCSA-N (2e,6e)-octa-2,6-dienal Chemical compound C\C=C\CC\C=C\C=O CBXNRMOWVZUZQA-BLWKUPHCSA-N 0.000 description 2
- JSNRRGGBADWTMC-UHFFFAOYSA-N (6E)-7,11-dimethyl-3-methylene-1,6,10-dodecatriene Chemical compound CC(C)=CCCC(C)=CCCC(=C)C=C JSNRRGGBADWTMC-UHFFFAOYSA-N 0.000 description 2
- WLTSXAIICPDFKI-FNORWQNLSA-N (E)-3-dodecene Chemical compound CCCCCCCC\C=C\CC WLTSXAIICPDFKI-FNORWQNLSA-N 0.000 description 2
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- JOHIXGUTSXXADV-HWKANZROSA-N (e)-undec-2-ene Chemical compound CCCCCCCC\C=C\C JOHIXGUTSXXADV-HWKANZROSA-N 0.000 description 2
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 2
- VQOXUMQBYILCKR-UHFFFAOYSA-N 1-Tridecene Chemical compound CCCCCCCCCCCC=C VQOXUMQBYILCKR-UHFFFAOYSA-N 0.000 description 2
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- PJLHTVIBELQURV-UHFFFAOYSA-N 1-pentadecene Chemical compound CCCCCCCCCCCCCC=C PJLHTVIBELQURV-UHFFFAOYSA-N 0.000 description 2
- JLIDVCMBCGBIEY-UHFFFAOYSA-N 1-penten-3-one Chemical compound CCC(=O)C=C JLIDVCMBCGBIEY-UHFFFAOYSA-N 0.000 description 2
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 2
- XCBBNTFYSLADTO-UHFFFAOYSA-N 2,3-Octanedione Chemical compound CCCCCC(=O)C(C)=O XCBBNTFYSLADTO-UHFFFAOYSA-N 0.000 description 2
- ICKWICRCANNIBI-UHFFFAOYSA-N 2,4-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C(C(C)(C)C)=C1 ICKWICRCANNIBI-UHFFFAOYSA-N 0.000 description 2
- OJVAMHKKJGICOG-UHFFFAOYSA-N 2,5-hexanedione Chemical compound CC(=O)CCC(C)=O OJVAMHKKJGICOG-UHFFFAOYSA-N 0.000 description 2
- RYPKRALMXUUNKS-UHFFFAOYSA-N 2-Hexene Natural products CCCC=CC RYPKRALMXUUNKS-UHFFFAOYSA-N 0.000 description 2
- IEDKVDCIEARIIU-UHFFFAOYSA-N 2-Nonadecanone Chemical compound CCCCCCCCCCCCCCCCCC(C)=O IEDKVDCIEARIIU-UHFFFAOYSA-N 0.000 description 2
- QQZOPKMRPOGIEB-UHFFFAOYSA-N 2-Oxohexane Chemical compound CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 description 2
- CJPNOLIZCWDHJK-UHFFFAOYSA-N 2-Pentadecanone Chemical compound CCCCCCCCCCCCCC(C)=O CJPNOLIZCWDHJK-UHFFFAOYSA-N 0.000 description 2
- POQLVOYRGNFGRM-UHFFFAOYSA-N 2-Tetradecanone Chemical compound CCCCCCCCCCCCC(C)=O POQLVOYRGNFGRM-UHFFFAOYSA-N 0.000 description 2
- WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical compound C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 description 2
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- CETWDUZRCINIHU-UHFFFAOYSA-N 2-heptanol Chemical compound CCCCCC(C)O CETWDUZRCINIHU-UHFFFAOYSA-N 0.000 description 2
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- YSPNCPGGCOBEKE-UHFFFAOYSA-N trimethyl(2-phenoxyethoxy)silane Chemical compound C[Si](C)(C)OCCOC1=CC=CC=C1 YSPNCPGGCOBEKE-UHFFFAOYSA-N 0.000 description 1
- YCRIXHKHAODKFH-UHFFFAOYSA-N trimethyl-[4-[2-methyl-4-(4-trimethylsilyloxyphenyl)pent-4-en-2-yl]phenoxy]silane Chemical compound C=1C=C(O[Si](C)(C)C)C=CC=1C(C)(C)CC(=C)C1=CC=C(O[Si](C)(C)C)C=C1 YCRIXHKHAODKFH-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229960003986 tuaminoheptane Drugs 0.000 description 1
- NQVBDTYIJUEQLV-UHFFFAOYSA-N undeca-5,9-dien-2-one Chemical compound CC=CCCC=CCCC(C)=O NQVBDTYIJUEQLV-UHFFFAOYSA-N 0.000 description 1
- YEHGKFOTJWYCBN-UHFFFAOYSA-N undecyl benzoate Chemical compound CCCCCCCCCCCOC(=O)C1=CC=CC=C1 YEHGKFOTJWYCBN-UHFFFAOYSA-N 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- SAXRUMLUKZBSTO-UHFFFAOYSA-N xi-3,5-Dimethyl-2(5H)-furanone Chemical group CC1OC(=O)C(C)=C1 SAXRUMLUKZBSTO-UHFFFAOYSA-N 0.000 description 1
- ZFNVDHOSLNRHNN-UHFFFAOYSA-N xi-3-(4-Isopropylphenyl)-2-methylpropanal Chemical compound O=CC(C)CC1=CC=C(C(C)C)C=C1 ZFNVDHOSLNRHNN-UHFFFAOYSA-N 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- YKFLAYDHMOASIY-UHFFFAOYSA-N γ-terpinene Chemical compound CC(C)C1=CCC(C)=CC1 YKFLAYDHMOASIY-UHFFFAOYSA-N 0.000 description 1
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- G01N1/00—Sampling; Preparing specimens for investigation
- G01N1/02—Devices for withdrawing samples
- G01N1/22—Devices for withdrawing samples in the gaseous state
- G01N1/2202—Devices for withdrawing samples in the gaseous state involving separation of sample components during sampling
- G01N1/2214—Devices for withdrawing samples in the gaseous state involving separation of sample components during sampling by sorption
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- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N1/00—Sampling; Preparing specimens for investigation
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- G01N1/24—Suction devices
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Abstract
【選択図】なし
Description
-収集チャンバと、
-気流吸引および吐出サイクルの交互に基づく遠隔ポンプシステムと、
-収着支持体と、
-流入空気を再循環するためのシステムを提供する回路と、を備えることを特徴とする、装置に関する。
ナール;2-メトキシ-3-メチル-酪酸、メチルエステル;2-n-ブチルフラン;2-n-ブチラクロレイン;2-n-オクチルフラン;2-ノナデカノン;2-ノナノン;2-ノネナール;2-ノネナール、(E)-;2-ノネナール、8-オキソ-;2-ノネン;2-酢酸ノルボルニル;2-オクタノン;2-オクテン-1-オール、(E)-;2-オクテン-1-オール、3,7-ジメチル-;2-オクテン-1-オール、3,7-ジメチル-、イソブチレート、(Z)-;2-オクテナル、(E)-;2-オクテン、(E)-;2-オクテン、2-メチル-6-メチレン-;2-オクチン-1-オール;2-オキサパノン;2-ペンタデカノン;2-ペンタノール、2,4-ジメチル-;2-ペンタノール、3-クロロ-2-メチル-;2-ペンタノン、3,3,4,4-テトラメチル-;2-ペンテナール、(E)-;2-フェノキシエチルイソブチレート;2-フェニルエチルアセテート;2-プロパノール、1-(2-ブトキシ-1-メチルエトキシ)-;2-プロパノール、1-(2-メトキシ-1-メチルエトキシ)-;2-プロパノール、1,1’-[(1-メチル-1,2-エタンジイル)ビス(オキシ)]ビス-;2-プロパノール、1,1’オキシビス-;2-プロパノール、1-[2-(2-メトキシ-1-メチルエトキシ)-1-メチルエトキシ]-;2-プロパノール、1-ブトキシ-;2-プロパノン、1-メトキシ-;2-プロパノール-1-オール、3-フェニル-;2-プロペン酸、(1-メチル-1,2-エタンジイル)ビス[オキシ(メチル-2,1-エタンジイル)]エステル;2-プロペン酸、2-メチル-、3,3,5-トリメチルシクロヘキシルエステル;2-プロペン酸、3-(2-ヒドロキシフェニル)-、(E)-;2-プロペン酸、トリデシルエステル;2-プロピル-1-ペンタノール;2-ピロール[tert-ブチル(ジメチル)シリル]オキシモルホプロパン-1-オール;2-ピロリドン、1-メチル-;2-テトラデカノン;2-トリデカノン;2-ウンデカノン;2-ウンデカノン、6,10-ジメチル-;2-ウンデセナール;2-ウンデセン、3-メチル-、(Z)-;2-ウンデセン、6-メチル-、(Z)-;3-((1S,5S,6R)-2,6-ジメチルビシクロ[3.1.1]ヘプト-2-エン-6-イル)プロパナール;3-(4-イソプロピルフェニル)-2-メチルプロピオンアルデヒド;3,5,9-ウンデカトリエン-2-オン、6,10-ジメチル-、(E,Z)-;3,5-ヘプタジエン-2-オン、6-メチル-、(E)-;3,6-ジオキサ-2,4,5,7-テトラシラオクタン、2,2,4,4,5,5,7,7-オクタメチル-;3,7-ノナジエン-2-オール、4,8-ジメチル-;3-アリル-6-メトキシフェノール;3-ブテン-1-オール、3-メチル-;3-ブテン-2-オン、4-(2,6,6-トリメチル-1シクロヘキセン-1-イル)-;3-カレン;3-シクロヘキセン-1-オール、1-メチル-4-(1-メチルエチル)-;3-シクロヘキセン-1-オール、4-メチル-1-(1-メチルエチル)-、(R)-;3-シクロヘキセン-1-カルボキサルデヒド;3-シクロヘキセン-1-カルボキサルデヒド、1-メチル-;3-シクロヘキセン-1-カルボキサルデヒド、2,4,6-トリメチル-;3-デセン、2,2-ジメチル-、(E)-;3-デセン酸;3-ドデカノール;3-ドデセン、(E)-;3-ドデセン、(Z)-;3-エチル-4,4-ジメチル-2-(2-メチルプロペニル)シクロヘキセノン-2-エノン;3-フルフリルエタノール;3-ヘプチン;3-ヘキサノン、5-メチル-;3-ヒドロキシ-3-フェニルブタン-2-オン;3-イソプロピル-4-メチル-1-ペンチン-3-オール;3-メトキシ-4-メチルヘプタン;3-メトキシアセトフェノン;3-メチル-2-ブテン酸、ウンデカ-2-エニルエステル;3-メチルシクロペンチルアセテート;3-ノナノール;3-ノナノン;3-オクタノール、3,6-ジメチル-;3-オクタノール、3,7-ジメチル-;3-オクタノール、アセテート;3-オクタノン;3-オクテン、2,2-ジメチル-;3-ペンタデカノン;3-ペンテン-2-オン;3-ペンテン-2-オン、(E)-;3-ペンテン-2-オン、4-(2,6,6-トリメチル-2-シクロヘキセノン-1-イル)-;3-ペンテン酸、4-メチル-;3-ウンデカン、4-メチル-;4-(t-ブチル)ベンズアルデヒド;4,14-ジメチル-11-イソプロピルトリシクロ[7.5.0.0(10,14)]テトラデカ-4-エン-8-オン;4,7-メタノ-1H-インデン-5-オール、3a,4,5,6,7,7a-ヘキサヒドロ-、アセテート;4,7-メタノ-1H-インデノール、ヘキサヒドロ-;4,8,12-テトラデカトリエナール、5,9,13-トリメチル-;4-ブトキシ-2-ブタノン;4-シアノシクロヘキセン;4-シクロペンテン-1,3-ジオン;4-エチル安息香酸、シクロブチルエステル;4-エチル安息香酸、デシルエステル;4-ヘプテン-3-オール、4-メチル-;4H-インデン-4-オン、1,2,3,5,6,7-ヘキサヒドロ-1,1,2,3,3-ペンタメチル-;4-メチル-2,4-ビス(p-ヒドロキシフェニル)ペント-1-エン、2TMS誘導体;4-オクタノール;4-オクタノン;4-フェニルセミカルバジド;4-テルピネニルアセテート;4-tert-ブチルシクロヘキシルアセテート;4-トリデセン、(Z)-;4-ウンデカン、5-メチル-;4-ウンデカン、8-メチル-、(Z)-;5,9-ウンデカジエン-1-イン、6,10-ジメチル-;5,9-ウンデカジエン-2-オン、6,10-ジメチル-、(Z)-;5-ドデシン;5-ホルミルサリチルアルデヒド;5H-1-ピリジン;5-ヘプテン-2-オン、6-メチル-;5-ヘプテナール、2,6-ジメチル-;5-ヘキセン-2-オン、5-メチル-;5-ヘキセン-2-オン、5-メチル-3-メチレン-;5-ヘキセナール、4-メチレン-;5-ヒドロキシ-2-ピリジンカルバルデヒド;5-メチル-1-フェニルオクタン;5-ノナノール;5-ノナノン;5-トリデセン、(Z)-;6-(5-メチルフラン-2-イル)-ヘキサン-2-オン;6,6-ジメチル-2-(3-オキソブチル)ビシクロ[3.1.1]ヘプタン(heptan)-3-オン;6-ドデセン、(E)-;6-ドデセン、(Z)-;6-メトキシ-2-ヘキサノール、TMS誘導体;6-メチル-3,5-ヘプタジエン-2-オン;6-ノネナール、(E)-;6-オクテン-1-オール、3,7-ジメチル-、アセテート;6-トリデカノール、3,9-ジエチル-;7,8-ジアザビシクロ[4.2.2]デカ-2,4,7,9-テトラエン-7-オキシド;7-アセチル-6-エチル-1,1,4,4-テトラメチルテトラリン;7a-イソプロペニル-4,5-ジメチルオクタヒドロインデン-4-カルボン酸;7-メチル-オクタデカン;7-オクテン-2-オール、2,6-ジメチル-;7-テトラデセン;7-テトラデセン、(Z)-;8-キノリノール、2-メチル-;9-デセン-2-オン、5-メチレン-;9-ドデシン-1-オール;9-メチルヘプタデカン;9-オキサビシクロ[3.3.1]ノナン-2-オン、3-メチル-6-(テトラヒドロ-2H-2-ピラニルオキシ)-;アセナフテン;アセトアルデヒド;アセトアルデヒド、(3,3-ジメチルシクロヘキシリデン)-、(E)-;アセトアミド、Ν,Ν-ジブチル-;アセトアミド、Ν,Ν-ジエチル-;酢酸;酢酸、2-アセトキシメチル-1,2,3-トリメチルブチルエステル;酢酸、2-エチルヘキシルエステル;酢酸、2-プロピルテトラヒドロピラン-3-イルエステル;酢酸、ブチルエステル;酢酸、フェニルメチルエステル;アセトン;アセトフェノン;アンブロキシド;アミレン水和物;アネトール;亜ヒ酸、トリス(トリメチルシリル)エステル;アズレン、1,2,3,5,6,7,8,8a-オクタヒドロ-1,4-ジメチル-7-(1-メチルエテニル)-、[1S-(1α,7α,8aβ)]-;ベンズアルデヒド;ベンズアルデヒド、2,4-ジクロロ-;ベンズアルデヒド、2-ヒドロキシ-;ベンズアルデヒド、2-メチル-;ベンズアルデヒド、3-ヒドロキシ-4-ベンジルオキシ-;ベンズアルデヒド、3-メチル-;ベンズアルデヒド、4-メトキシ-;ベンズアルデヒド、4-メチル-;ベンゼナミン、2-(1-メチルエテニル)-;ベンゼンアミン、N-エチル-;ベンゼン、(1-ブチルヘプチル)-;ベンゼン、(1-ブチルヘキシル)-;ベンゼン、(1-エチルデシル)-;ベンゼン、(1-エチルノニル)-;ベンゼン、(1-エチルウンデシル)-;ベンゼン、(1-メチルデシル)-;ベンゼン、(1-メチルノニル)-;ベンゼン、(1-ペンチルヘプチル)-;ベンゼン、(1-プロピルヘプチル)-;ベンゼン、(1-プロピルノニル)-;ベンゼン、(1-プロピルオクチル)-;ベンゼン、1-(1,5-ジメチル-4-ヘキセニル)-4-メチル-;ベンゼン、1,2,3,4-テトラメチル-;ベンゼン、1,2,4-トリメチル-;ベンゼン、1,2-ジメトキシ-4-(1-プロペニル)-;ベンゼン、1,3-ビス(1-メチルエテニル)-;ベンゼン、1,3-ビス(1-メチルエチル)-;ベンゼン、1,3-ジクロロ-;ベンゼン、1,3-ジクロロ-2-メチル-;ベンゼン、1,3-ジメチル-;ベンゼン、1,4-ビス(1-メチルエテニル)-;ベンゼン、1-エチル-3-メチル-;ベンゼン、1-メトキシ-4-ペンチル-;ベンゼン、1-メチル-4-(1-メチルエテニル)-;ベンゼン、2-エチル-1,4-ジメチル-;ベンゼン、ノニル-;ベンゼン、プロピル-;ベンゼン、tert-ブチル-;ベンゼン酢酸、α-オキソ-、メチルエステル;ベンゼンメタノール、α,α,4-トリメチル-;ベンゼンメタノール、α-エテニル-α-メチル-;ベンゼンメタノール、α-メチル-、アセテート;ベンゼンメタノール、4-(1,1-ジメチルエチル)-;ベンゼンペンタノール、γ-メチル-、アセテート;ベンゼンプロパノール、α,α-ジメチル-;ベンゼンスルホンアミド、N-エチル-2-メチル-;安息香酸;安息香酸、2,4-ジクロロ-、エチルエステル;安息香酸、2,6-ジクロロ-、メチルエステル;安息香酸、2-ヒドロキシ-、2-メチルブチルエステル;安息香酸、4-[6-(1,1-ジメチルエチル)-2H-1,3-ベンゾオキサジン-3(4H)-イル]-;安息香酸、ウンデシルエステル;ベンゾニトリル、4-(4-プロピル-1-シクロヘキセン-1-イル)-;ベンゾフェノン;ベンゾチアゾール;ベンゾチアゾール、2-メチル-;ベンジルアルコール;ベータ-カリオフィレン;ビシクロ[2.2.1]ヘプタン(heptan)-2-オン、1,3,7,7-テトラメチル-;ビシクロ[2.2.2]オクタン、1-メチル-4-(メチルスルホニル)-;ビシクロ[3.1.1]ヘプタン(heptan)-2-オン、3,6,6-トリメチル-;ビシクロ[3.1.1]ヘプタン(heptan)-2-オン、6,6-ジメチル-、(1R)-;ビシクロ[3.11]ヘプタン(heptan)-3-オン、2,6,6-トリメチル-;ビシクロ[3.1.1]ヘプタン、2,6,6-トリメチル-3-(2-プロペニル)-、(1α,2β,3α,5α)-;ビフェニル;ホウ酸、3TMS誘導体;ブタナール、2-エチル-;ブタン、1,1,3-トリメトキシ-;ブタン二酸、ヒドロキシ-、ジエチルエステル;ブチロニトリル、3-メチル-;ブタン酸;ブタン酸、3-クロロ-;ブタン酸、ペンチルエステル;酢酸ブチル;ブチル化ヒドロキシトルエン;ブチロラクトン;カンフェン;樟脳;カプロラクタム;カルバミン酸、フェニルエステル;カルバモジチオ酸、ジエチル-、メチルエステル;炭酸、エイコシルプロプ-1-エン-2-イルエステル;炭酸、ノニルプロプ-1-エン-2
-イルエステル;炭酸、オクタデシルビニルエステル;炭酸、オクチルビニルエステル;炭酸、プロプ-1-エン-2-イルウンデシルエステル;炭酸、トリデシルビニルエステル;カロトール;セドロール;シンナムアルデヒド、(E)-;シンナムアルデヒド、α-ペンチル-;シス-β-ファルネセン;シス-3-ヘキセニルサリチレート;シス-クリサンテノール;シス-シクロヘキサン-1,4-ジメタノール、ジアセテート;cis-ヘキサヒドロフタリド;cis-ツヨプセン;シトロネロール;シクロヘプタン、4-メチレン-1-メチル-2-(2-メチル-1プロペン-1-イル)-1-ビニル-;シクロヘプタノン;シクロヘプタノン、2-メチル-;シクロヘキサン、(2-メチルプロピル)-;シクロヘキサン、(4-メチルペンチル)-;シクロヘキサン、1,1’-(1,2-ジメチル-1,2-エタンジイル)ビス-;シクロヘキサン、1,1,2-トリメチル-;シクロヘキサン、1-エテニル-1-メチル-2,4-ビス(1-メチルエテニル)-、[1S-(1α,2β,4β)]-;シクロヘキサン、2-エテニル-1,1-ジメチル-3-メチレン-;シクロヘキサン、2-エチル-1,3-ジメチル-;シクロヘキサン、イソシアナト-;シクロヘキサン、メチル-;シクロヘキサン、ペンチル-;シクロヘキサンメタノール、4-(1-メチルエチル)-、シス-;シクロヘキサンメタノール、4-(1-メチルエチル)-、トランス-;シクロヘキサノール、1-メチル-4-(1-メチルエテニル)-;シクロヘキサノール、2-(1,1-ジメチルエチル)-;シクロヘキサノール、4-アミノ-、トランス-;シクロヘキサノン;シクロヘキサノン、5-メチル-2-(1-メチルエチル)-、シス-;シクロヘキセン、1-メチル-4-(1-メチルエチル)-、(R)-;シクロヘキセン、1-メチル-4-(1-メチルエチリデン)-;シクロヘキセン、4-[(1E)-1,5-ジメチル-1,4-ヘキサジエン-1-イル]-1-メチル-;シクロオクタン、メチル-;シクロオクテン、3-メチル-;シクロペント-4-エン-1,3-ジオン;シクロペンタ[g]-2-ベンゾピラン、1,3,4,6,7,8-ヘキサヒドロ-4,6,6,7,8,8-ヘキサメチル-;シクロペンタデカノール;シクロペンタン、1,2-ジブチル-;シクロペンタン、1,3-ジメチル-、トランス-;シクロペンタン、1-アセチル-1,2-エポキシ-;シクロペンタン、1-ブチル-2-プロピル-;シクロペンタン、1-エチル-2-メチル-、シス-;シクロペンタン、1-メチル-1-(2-メチル-2-プロペニル)-;シクロペンタン、1-ペンチル-2-プロピル-;シクロペンタン、3-ヘキシル-1,1-ジメチル-;シクロペンタン、デシル-;シクロペンタン、ノニル-;シクロペンタン酢酸、3-オキソ-2-ペンチル-、メチルエステル;シクロペンタンカルボン酸、ノニルエステル;シクロペンタノン;シクロペンタノン、2-(2-オクテニル)-;シクロペンタノン、2-メチル-3-(1-メチルエチル)-;シクロペンテン、1-オクチル-;シクロプロパンカルボキサルデヒド、2-メチル-2-(4-メチル-3-ペンテニル)-、トランス-(±)-;シクロプロパンメタノール、α,2-ジメチル-2-(4-メチル-3-ペンテニル)-、[1α(R*),2α]-;デカナール;デカン;デカン、1,1’-オキシビス-;デカン、2,2-ジメチル-;デカン、2,6,7-トリメチル-;デカン、3,6-ジメチル-;デカン、4-メチル-;デカネニトリル;デカン酸;デカン酸、メチルエステル;デカン酸、銀(1+)塩;D-ガラクトース;D-グルシトール、環状1,3:2,4-ビス(フェニルボロネート)5,6-ジアセテート;ジベンゾフラン;アジピン酸ジブチル;ジクロロ酢酸、4-ペンタデシルエステル;ジエピ-α-セドレン;2,5-ピリジンジカルボン酸ジエチル;フタル酸ジエチル;ジエチルシアナミド;フタル酸ジメチル;ジメチルスルホン;ジメチルアミノメチル-ホスホン酸ジイソブチルエステル;ジフェニルエーテル;D-リモネン;ドコサン;ドデカナール;ドデカナミド、N-(2-ヒドロキシエチル)-;ドデカン;ドデカン、1-クロロ-;ドデカン、1-メトキシ-;ドデカン、2,6,11-トリメチル-;ドデカン、4,9-ジプロピル-;ドデカニトリル;ドデカン酸;ドデカン酸、1-メチルエチルエステル;ドデカン酸、メチルエステル;ドデシルノニルエーテル;ドデシルオクチルエーテル;E-11(12-シクロプロピル)ドデセン-1-オール;エイコサン;エイコサン、10-メチル-;エストラゴール;エストラン-3-オン、17-(アセチルオキシ)-2-メチル-、(2α,5α,17β)-;エタン二酸、ジエチルエステル;エタノール;エタノール、1-(2-ブトキシエトキシ)-;エタノール、2-(2-ブトキシエトキシ)-、アセテート;エタノール、2-(ドデシルオキシ)-;エタノール、2-(ヘキサデシルオキシ)-;エタノール、2-(ヘキシルオキシ)-;エタノール、2-(テトラデシルオキシ)-;エタノール、2-ブトキシ-;エタノール、2-ニトロ-、プロピオネート(エステル);エタノール、2-フェノキシ-;エタノン、1-(1-シクロヘキセン-1-イル)-;エタノン、1-(2,3-ジヒドロ-1H-インデン-5-イル)-;エタノン、1-(2,5-ジクロロフェニル)-;エタノン、1-(2-メチルフェニル)-;エタノン、1-(3-メチレンシクロペンチル)-;エタノン、1-(3-メチルフェニル)-;エタノン、1,1’-(1,3-フェニレン)ビス-;エタノン、1-(4-(1,1ジメチルエチル)フェニル]-;エタノン、1-(4-(1-ヒドロキシ-1-メチルエチル)フェニル]-;エタノン、2,2-ジメトキシ-1,2-ジフェニル-;エチル(S)-(-)-ラクテート;エチル4-アセチルベンゾエート;エチル7-(2-オキソシクロペンチル)ヘプタノエート;エチルアセトキシカルバメート;エチルブチルケトン;エチルパルミテート;エチルバニリン;エチルベンゼン;エチルブラシレート;ユーカリプトール;フェンコール;ホルムアルデヒド;ホルムアミド、Ν,Ν-ジブチル-;ホルムアミド、Ν,Ν-ジエチル-;ギ酸、ブチルエステル;ギ酸、エテニルエステル;ギ酸、ヘキシルエステル;ギ酸、テトラヒドロフルフリルエステル;フマル酸、ブチルシス-ヘキサ-3-エニルエステル;フラン、2,3-ジヒドロ-;フラン、2-メチル-;フラン、2-ペンチル-;フルフラール;ゲラニオール;酢酸ゲラニル;グリセロール1,2-ジアセテート;グリシドール;グリコールアルデヒドジメチルアセタール;グリコール酸、2TMS誘導体;ヘンイコサン;ヘプタデカン;ヘプタデカン、2-メチル-;ヘプタデカン、3-メチル-;ヘプタデカン、7-メチル-;ヘプタナール;ヘプタン;ヘプタン、1-クロロ-;ヘプタン、2,4,6-トリメチル-;ヘプタン、4-メチル-;ヘプタンジアミド、N,N’-ジ-ベンゾイルオキシ-;ヘプタン酸;ヘプタノニトリル;ヘキサデカナール、2-メチル-;ヘキサデカン;ヘキサデカン、2,6,10,14-テトラメチル-;ヘキサデカン、2-メチル-;ヘキサデカン酸、メチルエステル;ヘキサデセン;ヘキサナール;ヘキサナール、2-エチル-;ヘキサン、2,3-ジメチル-;ヘキサン、2-メチル-;ヘキサン、3,3,4-トリメチル-;ヘキサン、3-メチル-;ヘキサン酸;ヘキサン酸、2-エチル-;ヘキサン酸、3,5,5-トリメチル-、2-エチルヘキシルエステル;ヘキシルオクチルエーテル;ヘキシレングリコール;ヒドラジンカルボチオアミド、N-メチル-;アジ化水素;インダン;インドール-2-オン、3-[2-(4-tert-ブチルフェニル)-2-オキソエチル]-3-ヒドロキシ-5-メチル-1,3-ジヒドロ-;インドール;酢酸イソボルニル;酢酸イソブチル;イソロンギフォロール;アイソネラル;イソホロン;イソピノカルベオール;イソプロポキシカルバミン酸、エチルエステル;イソプロピルアルコール;ミリスチン酸イソプロピル;パルミチン酸イソプロピル;イソプロピルシクロブタン;イソプレゴール;酢酸イソプレゴール;L-α-テルピネオール;乳酸;リリアール;リモネン;リナロール;酢酸リナリル;リンコマイシン;ロンギフォレンアルデヒド;ロンギホレン;l-パントイルラクトン;l-バリン、N-(3-メチル-1-オキソブチル)-、メチルエステル;マロン酸、ビス(2-トリメチルシリルエチルエステル;m-アミノフェニルアセチレン;m-クロロアニリン;メンソール;メシチレン;メタクロレイン;メタノン、(1-ヒドロキシシクロヘキシル)フェニル-;メトキシ酢酸、2-エチルヘキシルエステル;5-アセチル-2-メトキシ安息香酸メチル;メチル7,9-トリデカジエニルエーテル;メチルアルコール;メチルアントラニル酸;メチルイソブチルケトン;メチルオクタノエート;メチルサリチレート;テトラデカン酸メチル;メチルアミン、N-(1-メチルヘプチリデン)-;メチルパラベン;ミロキシド;Ν,Ν’-ジアセチルエチレンジアミン;N,N-ジエチル-N’-ホルミル-N’-メトキシ尿素;ナフタレン;ナフタレン、1,2,3,5,6,8a-ヘキサヒドロ-4,7-ジメチル-1-(1-メチルエチル)-、(1S-シス)-;ナフタレン、1,6,7-トリメチル-;ナフタレン、1,7-ジメチル-;ナフタレン、1-メチル-;ナフタレン、2,3-ジメチル-;ナフタレン、2,7-ジクロロ-;ナフタレン、2-メトキシ-;ナフタレン、デカヒドロ-、トランス-;n-ブチルエーテル;n-カプロン酸ビニルエステル;n-デカン酸;ネオフィタジエン;n-ヘキサン;n-サリチル酸ヘキシル;一酸化窒素;n-ノナデカノール-1;n-ノニルシクロヘキサン;ノナ-3,5-ジエン-2-オン;ノナナール;ノナン;ノナン、1-クロロ-;ノナン、2-メチル-5-プロピル-;ノナン、3-メチル-;ノナン、5-(1-メチルプロピル)-;ノナン、5-(2-メチルプロピル)-;ノナンニトリル;ノナン酸;n-ペンタデカノール;n-トリデカン-1-オール;オクト-3-エン酸、オクト-3-エン-2-イルエステル;オクタデカン;オクタデカン、6-メチル-;オクタナール;オクタナール、2-(フェニルメチレン)-;オクタナール、7-メトキシ-3,7-ジメチル-;オクタン;オクタン、1,1’-オキシビス-;オクタン、1-クロロ-;オクタン、2,7-ジメチル-;オクタン、3,5-ジメチル-;オクタン、4-メチル-;オクタネニトリル;オクタン酸;オクタン酸、オクチルエステル;オクチルテトラデシルエーテル;o-シメン;o-ヒドロキシビフェニル;オレイン酸、2-ヒドロキシエチルエステルステアレート;o-tert-ブチルシクロヘキシルアセテート1;オキサシクロヘプタデカ-8-エン-2-オン、(8Z);オキサシクロヘプタデカン-2-オン;シュウ酸、2-エチルヘキシルヘキシルエステル;シュウ酸、2-エチルヘキシルイソヘキシルエステル;シュウ酸、2-エチルヘキシルオクチルエステル;シュウ酸、2-エチルヘキシルペンタデシルエステル;シュウ酸、2TMS誘導体;オキセピン、2,7-ジメチル-;オキシム-、メトキシ-フェニル-_;オキシラン、3-エチル-2,2-ジメチル-;オキシラン、デシル-;オキシランメタノール、3-メチル-3-(4-メチル-3-ペンテニル)-;o-キシレン;p-クレゾール;ペンタデカナール-;ペンタデカン;ペンタデカン、2,6,10,14-テトラメチル-;ペンタデカン、3-メチル-;ペンタデカン、6-メチル-;ペンタデカン、8-ヘキシル-;ペンタデカン酸;ペンタナール;ペンタン、1-クロロ-;ペンタン、2,3,3-トリメチル-;ペンタン二酸、ジメチルエステル;ペンタン酸;ペンタン酸、2,4-ジメチル-3-オキソ-、メチルエステル;フェノール;フェノール、2-(1,1-ジメチルエチル)-;フェノール、2-(
1,1-ジメチルエチル)-6-メチル-;フェノール、2,4-ジクロロ-;フェノール、3-メチル-;フェノール、4-(1,1,3,3-テトラメチルブチル)-;フェノキシエタノール、TMS誘導体;フェニルエチルアルコール;無水フタル酸;ピロナール;p-メンス-8-エン-1-オール、立体異性体;p-メンタ-1,5,8-トリエン;p-メンタ-1,5-ジエン-8-オール;プロパナール、2-メチル-3-フェニル-;プロパナール、3-メトキシ-;プロパナミド、N-アセチル-;プロパン、1,1,3,3-テトラメトキシ-;プロパン、1,1-ジメトキシ-2-メチル-;プロパン、2-エトキシ-2-メチル-;プロパン-1,3-ジオール、2-メチル-;プロパネジン酸、2TMS誘導体;プロパン酸;プロパン酸、2,2-ジメチル-;プロパン酸、2-(4-(1-ホルミルエチル)フェニル]-、メチルエステル;プロパン酸、2-メチル-、1-(1,1-ジメチルエチル)-2-メチル-1,3-プロパンジイルエステル;プロパン酸、2-メチル-、2-エチル-3-ヒドロキシヘキシルエステル;プロパン酸、2-メチル-、オクチルエステル;プロパン酸、3-(2-ヒドロキシシクロブチリデン)-2-メチル-、[R*,R*-(E)]-;プロパノール、[(ブトキシメチルエトキシ)メチルエトキシ]-;炭酸プロピレン;プロピレングリコール;プロピレンオゾニド;プロピルパラベン;p-キシレン;ピラジン、2,6-ジメチル-;ピリジン;ピリジン、3-メチル-;ピロール;ピロリジン、1,1’-メチレンビス-;キノリン;キノリン、1,2-ジヒドロ-2,2,4-トリメチル-;ロタンドン(rotundene);サリチル酸、1-メチルプロピルエーテル、1-メチルプロピルエステル;sec-酢酸ブチル;スピロ[2.4]ヘプタン-5-メタノール、5-ヒドロキシ-;スクアレン;ステアリン酸ヒドラジド;スチレン;テトラコサン;テトラデカン;テトラデカン、2-メチル-;テトラデカン、3-メチル-;テトラデカン、5-メチル-;テトラデカン酸;テトラヒドロピロロ[1,2-a]アゼチジン-2-オン;テトラメチルチオ尿素;テトラメチルピラジン;チオ酢酸;チオシアン酸、エチルエステル;チオフェン、テトラヒドロ-2-メチル-;トルエン;トランス-β-イオノン;トランス-2-ドデセン-1-オール;トランス-8-メチル-1β-アセチル-ヒドリンダン;トランスデカリン、2-メチル-;トリ(1,2-プロピレングリコール)、モノメチルエーテル;トリアセチン;トリデカナール;トリデカン;トリデカン、3-メチレン-;トリデカン、6-メチル-;トリデカンニトリル;トリデカン酸;トリデカン酸、3-ヒドロキシ-、エチルエステル;クエン酸トリエチル;ウンデク-10-イン酸、イソブチルエステル;ウンデカナール;ウンデカナール、2-メチル-;ウンデカン;ウンデカン、2,5-ジメチル-;ウンデカン、2,7-ジメチル-;ウンデカン、2-メチル-;ウンデカン、3,6-ジメチル-;ウンデカン、3-メチル-;ウンデカン、3-メチレン-;ウンデカン、6-エチル-;ウンデカン、6-メチル-;ウンデカニトリル;ウンデカン酸;バニリン;Z-2-オクタデセン-1-オールアセテート。
-本発明による装置を使用して、揮発性有機化合物を収集することと、
-前記収着支持体を前記収集装置から引き出すステップと、
-前記揮発性有機化合物を脱着するステップと、
-ガスクロマトグラフィーステップと、
-質量分析ステップと、を含む、方法に関する。
Claims (13)
- 揮発性有機化合物を空気から収集するための装置であって、
-収集チャンバと、
-気流吸引および吐出サイクルの交互に基づく遠隔ポンプシステムと、
-収着支持体と、
-流入空気を再循環するためのシステムを提供する回路と、を備えることを特徴とする、装置。 - 前記収着支持体が、吸収支持体であることを特徴とする、請求項1に記載の装置。
- 前記収着支持体が、吸着支持体であることを特徴とする、請求項1に記載の装置。
- 前記吸収支持体が、シクロデキストリン、亜硫酸水素ナトリウム、および/またはジニトロフェニルヒドラジンから選択されることを特徴とする、請求項2に記載の装置。
- 前記吸着支持体が、圧縮物、ポリジメチルシロキサンパッチ、カーボンブラック、分子ふるい、および/もしくは有機ポリマー、またはそれらの組み合わせから選択されることを特徴とする、請求項3に記載の装置。
- 前記回路が、前記気流の前記再循環中に前記収集チャンバを密封することによって閉じられることを特徴とする、請求項1~5のいずれか一項に記載の装置。
- 前記回路が、単回使用コネクタで形成されることを特徴とする、請求項1~6のいずれか一項に記載の装置。
- 空気中に存在する前記揮発性有機化合物を少なくとも1兆分の1の比率で特徴付けるための方法であって、
-本発明による前記装置を使用して、前記揮発性有機化合物を収集するステップと、
-前記収着支持体を前記収集装置から引き出すステップと、
-前記揮発性有機化合物を脱着するステップと、
-ガスクロマトグラフィーステップと、
-質量分析ステップと、を含む、方法。 - 空気試料によって実装されることを特徴とする、請求項8に記載の方法。
- 前記脱着ステップが、熱脱着ステップであることを特徴とする請求項8および9に記載の方法。
- 前記ガスクロマトグラフィーステップが、二次元ガスクロマトグラフィーステップであることを特徴とする、請求項8~10に記載の方法。
- 個体の前記臭気物質シグネチャを特徴付けるための請求項1~7に記載の装置の使用。
- 収着支持体を豊富にし、かつイヌがその臭気物質シグネチャから個体を識別することを可能にするための請求項1~7に記載の装置の使用。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR1871496 | 2018-11-13 | ||
FR1871496A FR3088429B1 (fr) | 2018-11-13 | 2018-11-13 | Dispositif permettant de prelever les composes organiques volatils |
PCT/FR2019/000184 WO2020099735A1 (fr) | 2018-11-13 | 2019-11-13 | Dispositif permettant de prélever les composés organiques volatils |
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EP3742969A1 (en) | 2018-03-06 | 2020-12-02 | Entech Instruments Inc. | Ventilator-coupled sampling device and method |
JP7522682B2 (ja) * | 2021-03-01 | 2024-07-25 | 株式会社東芝 | ケミカルセンサ装置およびケミカルセンサモジュール |
FR3122258B1 (fr) * | 2021-04-26 | 2024-03-01 | Biodesiv Sarl | Procédé d’extraction et de détection de molécules odorantes réelles d’intérêt et dispositif d’extraction mettant en œuvre ledit procédé |
CN115656359A (zh) * | 2022-10-13 | 2023-01-31 | 上海市环境科学研究院 | 分离和同时检测乙醛和环氧乙烷的方法 |
CN115812711B (zh) * | 2022-12-09 | 2024-05-31 | 河南农业大学 | 一种蛞蝓引诱剂及其制备方法 |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03142337A (ja) * | 1989-10-28 | 1991-06-18 | Miyamoto Riken Kogyo Kk | 水中の微量物質捕集装置 |
JPH1164313A (ja) * | 1997-08-11 | 1999-03-05 | Sumitomo Metal Mining Co Ltd | 建材より発生する室内汚染ガス成分の測定方法及び装置並びに評価方法 |
JP2001235405A (ja) * | 2000-02-21 | 2001-08-31 | Ube Kagaku Bunseki Center:Kk | 揮発性有機化合物の捕集方法、及びそれを利用した分析方法、並びに揮発性有機化合物の捕集装置 |
JP2003240685A (ja) * | 2002-02-18 | 2003-08-27 | Konica Corp | 化学物質の捕集装置及び化学物質の捕集方法 |
JP3123627U (ja) * | 2006-01-24 | 2006-07-27 | 信弥 吉田 | 接着剤層又は粘着剤層付き刺股状防護具 |
WO2011099079A1 (ja) * | 2010-02-12 | 2011-08-18 | ジーエルサイエンス株式会社 | 試料の捕集方法およびその捕集装置 |
JP2015059770A (ja) * | 2013-09-17 | 2015-03-30 | 株式会社トクヤマ | 環境大気中の揮発性有機化合物の測定方法 |
US20160320271A1 (en) * | 2015-05-01 | 2016-11-03 | Ctc Analytics Ag | Device for extracting volatile components |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2177153A (en) * | 1936-07-13 | 1939-10-24 | Oscar A Ross | Vacuum cleaner dolly |
JP2003185539A (ja) * | 2001-12-18 | 2003-07-03 | Sumika Chemical Analysis Service Ltd | 室内空気分析用サンプリングキット |
KR100443987B1 (ko) * | 2002-02-14 | 2004-08-09 | 삼성전자주식회사 | 콜리메이터용 솔더링장치 및 솔더링방법 |
US7168833B2 (en) * | 2002-04-05 | 2007-01-30 | General Electric Company | Automotive headlamps with improved beam chromaticity |
JP2004023228A (ja) * | 2002-06-13 | 2004-01-22 | Matsushita Electric Ind Co Ltd | アンテナ制御装置、及びフェイズドアレイアンテナ |
DE602006019307D1 (de) | 2005-11-18 | 2011-02-10 | Florida Int Univ Board Trustees | Indentifizierung von menschen durch charakteristische verbindungen aus dem menschlichen duft |
US7448288B2 (en) | 2006-10-12 | 2008-11-11 | Vincent Montefusco | Scent evidence transfer device |
US8334505B2 (en) * | 2007-10-10 | 2012-12-18 | Mks Instruments, Inc. | Chemical ionization reaction or proton transfer reaction mass spectrometry |
US9267866B2 (en) * | 2013-03-13 | 2016-02-23 | The Florida International University Board Of Trustees | Capillary microextractor of volatiles (CMV) |
GB201602394D0 (en) * | 2016-02-10 | 2016-03-23 | Mdb Medical Services Ltd | Method |
US10345201B2 (en) * | 2016-08-28 | 2019-07-09 | Alireza Ghiasvand | Polypyrrole/graphene oxide nanocomposite-coated fiber located in a capillary tube reinforced by a vacuum system for assessment of oxidative stability of edible oils |
-
2018
- 2018-11-13 FR FR1871496A patent/FR3088429B1/fr active Active
-
2019
- 2019-11-13 WO PCT/FR2019/000184 patent/WO2020099735A1/fr unknown
- 2019-11-13 EP EP19827774.1A patent/EP3881048A1/fr active Pending
- 2019-11-13 CN CN201980074324.0A patent/CN113167695A/zh active Pending
- 2019-11-13 US US17/293,075 patent/US20210396629A1/en active Pending
- 2019-11-13 KR KR1020217015641A patent/KR20210088596A/ko active Search and Examination
- 2019-11-13 JP JP2021549924A patent/JP2022509550A/ja active Pending
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03142337A (ja) * | 1989-10-28 | 1991-06-18 | Miyamoto Riken Kogyo Kk | 水中の微量物質捕集装置 |
JPH1164313A (ja) * | 1997-08-11 | 1999-03-05 | Sumitomo Metal Mining Co Ltd | 建材より発生する室内汚染ガス成分の測定方法及び装置並びに評価方法 |
JP2001235405A (ja) * | 2000-02-21 | 2001-08-31 | Ube Kagaku Bunseki Center:Kk | 揮発性有機化合物の捕集方法、及びそれを利用した分析方法、並びに揮発性有機化合物の捕集装置 |
JP2003240685A (ja) * | 2002-02-18 | 2003-08-27 | Konica Corp | 化学物質の捕集装置及び化学物質の捕集方法 |
JP3123627U (ja) * | 2006-01-24 | 2006-07-27 | 信弥 吉田 | 接着剤層又は粘着剤層付き刺股状防護具 |
WO2011099079A1 (ja) * | 2010-02-12 | 2011-08-18 | ジーエルサイエンス株式会社 | 試料の捕集方法およびその捕集装置 |
JP2015059770A (ja) * | 2013-09-17 | 2015-03-30 | 株式会社トクヤマ | 環境大気中の揮発性有機化合物の測定方法 |
US20160320271A1 (en) * | 2015-05-01 | 2016-11-03 | Ctc Analytics Ag | Device for extracting volatile components |
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WO2020099735A1 (fr) | 2020-05-22 |
CN113167695A (zh) | 2021-07-23 |
US20210396629A1 (en) | 2021-12-23 |
KR20210088596A (ko) | 2021-07-14 |
EP3881048A1 (fr) | 2021-09-22 |
FR3088429A1 (fr) | 2020-05-15 |
FR3088429B1 (fr) | 2020-12-18 |
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