IL138845A - A method of marking liquids with at least two markers and a method of identification - Google Patents

A method of marking liquids with at least two markers and a method of identification

Info

Publication number: IL138845A
Authority: IL; Israel
Prior art keywords: markers; marker; excitation; case; absorption
Prior art date: 1998-04-23

Application number

IL13884599A

Other languages

English (en)

Hebrew (he)

Other versions

IL138845A0 (en

Original Assignee

Basf Ag

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.)

1998-04-23

Filing date

1999-04-12

Publication date

2004-06-20

1999-04-12 Application filed by Basf Ag filed Critical Basf Ag

2001-10-31 Publication of IL138845A0 publication Critical patent/IL138845A0/xx

2004-06-20 Publication of IL138845A publication Critical patent/IL138845A/en

Links

239000003550 marker Substances 0.000 title claims abstract description 71
239000007788 liquid Substances 0.000 title claims abstract description 58
238000000034 method Methods 0.000 title claims abstract description 52
239000000126 substance Substances 0.000 title description 3
238000010521 absorption reaction Methods 0.000 claims abstract description 68
238000001228 spectrum Methods 0.000 claims abstract description 16
239000012620 biological material Substances 0.000 claims abstract 2
239000000203 mixture Substances 0.000 claims description 29
230000005855 radiation Effects 0.000 claims description 27
150000001875 compounds Chemical class 0.000 claims description 24
239000000980 acid dye Substances 0.000 claims description 13
229930195733 hydrocarbon Natural products 0.000 claims description 8
150000002430 hydrocarbons Chemical class 0.000 claims description 8
239000000975 dye Substances 0.000 claims description 7
239000004065 semiconductor Substances 0.000 claims description 7
229910052751 metal Inorganic materials 0.000 claims description 6
239000002184 metal Substances 0.000 claims description 6
RBSLJAJQOVYTRQ-UHFFFAOYSA-N croconic acid Chemical compound OC1=C(O)C(=O)C(=O)C1=O RBSLJAJQOVYTRQ-UHFFFAOYSA-N 0.000 claims description 5
125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims description 5
239000007787 solid Substances 0.000 claims description 5
PWEBUXCTKOWPCW-UHFFFAOYSA-N squaric acid Chemical compound OC1=C(O)C(=O)C1=O PWEBUXCTKOWPCW-UHFFFAOYSA-N 0.000 claims description 5
239000004215 Carbon black (E152) Substances 0.000 claims description 4
150000004982 aromatic amines Chemical class 0.000 claims description 3
-1 phenylimino Chemical group 0.000 description 179
230000005284 excitation Effects 0.000 description 91
238000001514 detection method Methods 0.000 description 68
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 28
238000010276 construction Methods 0.000 description 22
150000003254 radicals Chemical class 0.000 description 22
230000003287 optical effect Effects 0.000 description 18
239000001257 hydrogen Substances 0.000 description 16
229910052739 hydrogen Inorganic materials 0.000 description 16
125000001033 ether group Chemical group 0.000 description 14
125000004430 oxygen atom Chemical group O* 0.000 description 14
239000013307 optical fiber Substances 0.000 description 13
239000002480 mineral oil Substances 0.000 description 12
239000003502 gasoline Substances 0.000 description 11
150000002431 hydrogen Chemical class 0.000 description 9
229910052736 halogen Inorganic materials 0.000 description 8
150000002367 halogens Chemical class 0.000 description 8
125000004433 nitrogen atom Chemical group N* 0.000 description 8
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 7
239000000446 fuel Substances 0.000 description 7
125000000623 heterocyclic group Chemical group 0.000 description 7
229910052760 oxygen Inorganic materials 0.000 description 7
239000001301 oxygen Substances 0.000 description 7
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 6
125000004435 hydrogen atom Chemical group [H]* 0.000 description 6
125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 6
125000001424 substituent group Chemical group 0.000 description 6
229910052717 sulfur Inorganic materials 0.000 description 6
SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 5
125000000217 alkyl group Chemical group 0.000 description 5
238000009826 distribution Methods 0.000 description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
229910052757 nitrogen Inorganic materials 0.000 description 5
125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 5
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 4
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 4
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 4
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
239000003921 oil Substances 0.000 description 4
235000019198 oils Nutrition 0.000 description 4
229920006395 saturated elastomer Polymers 0.000 description 4
125000004434 sulfur atom Chemical group 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 3
125000005916 2-methylpentyl group Chemical group 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
238000000862 absorption spectrum Methods 0.000 description 3
150000001450 anions Chemical class 0.000 description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
230000008033 biological extinction Effects 0.000 description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
229910052794 bromium Inorganic materials 0.000 description 3
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
239000000460 chlorine Substances 0.000 description 3
229910052801 chlorine Inorganic materials 0.000 description 3
125000004093 cyano group Chemical group *C#N 0.000 description 3
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
239000002283 diesel fuel Substances 0.000 description 3
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
239000007850 fluorescent dye Substances 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
125000001841 imino group Chemical group [H]N=* 0.000 description 3
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 3
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 3
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 3
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
229910052710 silicon Inorganic materials 0.000 description 3
239000010703 silicon Substances 0.000 description 3
239000011550 stock solution Substances 0.000 description 3
238000006467 substitution reaction Methods 0.000 description 3
125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
UUZJJNBYJDFQHL-UHFFFAOYSA-N 1,2,3-triazolidine Chemical compound C1CNNN1 UUZJJNBYJDFQHL-UHFFFAOYSA-N 0.000 description 2
WNBQDDAKLKODPH-UHFFFAOYSA-N 1,2,4-triazolidine Chemical compound C1NCNN1 WNBQDDAKLKODPH-UHFFFAOYSA-N 0.000 description 2
QNLZIZAQLLYXTC-UHFFFAOYSA-N 1,2-dimethylnaphthalene Chemical compound C1=CC=CC2=C(C)C(C)=CC=C21 QNLZIZAQLLYXTC-UHFFFAOYSA-N 0.000 description 2
SKLDBJVFTOQKHE-UHFFFAOYSA-N 1,3,4-oxadiazolidine Chemical compound C1NNCO1 SKLDBJVFTOQKHE-UHFFFAOYSA-N 0.000 description 2
BRQBVEHLEITSPT-UHFFFAOYSA-N 1,3,4-thiadiazolidine Chemical compound C1NNCS1 BRQBVEHLEITSPT-UHFFFAOYSA-N 0.000 description 2
OGYGFUAIIOPWQD-UHFFFAOYSA-N 1,3-thiazolidine Chemical compound C1CSCN1 OGYGFUAIIOPWQD-UHFFFAOYSA-N 0.000 description 2
125000004343 1-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C([H])([H])[H] 0.000 description 2
125000005999 2-bromoethyl group Chemical group 0.000 description 2
125000000143 2-carboxyethyl group Chemical group [H]OC(=O)C([H])([H])C([H])([H])* 0.000 description 2
125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 description 2
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 2
QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
WYNCHZVNFNFDNH-UHFFFAOYSA-N Oxazolidine Chemical compound C1COCN1 WYNCHZVNFNFDNH-UHFFFAOYSA-N 0.000 description 2
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 2
YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
238000002835 absorbance Methods 0.000 description 2
230000006978 adaptation Effects 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
125000003342 alkenyl group Chemical group 0.000 description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 description 2
125000003828 azulenyl group Chemical group 0.000 description 2
BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
238000002485 combustion reaction Methods 0.000 description 2
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
229940113083 morpholine Drugs 0.000 description 2
239000010705 motor oil Substances 0.000 description 2
125000001624 naphthyl group Chemical group 0.000 description 2
239000003208 petroleum Substances 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
USPWKWBDZOARPV-UHFFFAOYSA-N pyrazolidine Chemical compound C1CNNC1 USPWKWBDZOARPV-UHFFFAOYSA-N 0.000 description 2
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
230000035945 sensitivity Effects 0.000 description 2
239000002904 solvent Substances 0.000 description 2
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 2
239000011593 sulfur Substances 0.000 description 2
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
239000008096 xylene Substances 0.000 description 2
125000006656 (C2-C4) alkenyl group Chemical group 0.000 description 1
LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
125000006433 1-ethyl cyclopropyl group Chemical group [H]C([H])([H])C([H])([H])C1(*)C([H])([H])C1([H])[H] 0.000 description 1
125000006432 1-methyl cyclopropyl group Chemical group [H]C([H])([H])C1(*)C([H])([H])C1([H])[H] 0.000 description 1
125000005976 1-phenylethyloxy group Chemical group 0.000 description 1
YPJUNDFVDDCYIH-UHFFFAOYSA-M 2,2,3,3,4,4,4-heptafluorobutanoate Chemical compound [O-]C(=O)C(F)(F)C(F)(F)C(F)(F)F YPJUNDFVDDCYIH-UHFFFAOYSA-M 0.000 description 1
SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 description 1
SYOANZBNGDEJFH-UHFFFAOYSA-N 2,5-dihydro-1h-triazole Chemical compound C1NNN=C1 SYOANZBNGDEJFH-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 1
125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 1
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
125000004777 2-fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 description 1
125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 description 1
125000005975 2-phenylethyloxy group Chemical group 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
SZTRCMOSUUQMBM-UHFFFAOYSA-N 2h-azepine Chemical compound C1C=CC=CC=N1 SZTRCMOSUUQMBM-UHFFFAOYSA-N 0.000 description 1
JDFDHBSESGTDAL-UHFFFAOYSA-N 3-methoxypropan-1-ol Chemical compound COCCCO JDFDHBSESGTDAL-UHFFFAOYSA-N 0.000 description 1
GBSGXZBOFKJGMG-UHFFFAOYSA-N 3-propan-2-yloxypropan-1-ol Chemical compound CC(C)OCCCO GBSGXZBOFKJGMG-UHFFFAOYSA-N 0.000 description 1
125000004042 4-aminobutyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])N([H])[H] 0.000 description 1
125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 description 1
SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 description 1
125000004217 4-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1OC([H])([H])[H])C([H])([H])* 0.000 description 1
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IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
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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
- G01N33/26—Oils; Viscous liquids; Paints; Inks
- G01N33/28—Oils, i.e. hydrocarbon liquids
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/64—Fluorescence; Phosphorescence
- G01N21/6428—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes"
- G01N21/643—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" non-biological material
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/003—Marking, e.g. coloration by addition of pigments
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/64—Fluorescence; Phosphorescence
- G01N21/6428—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes"
- G01N2021/6439—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" with indicators, stains, dyes, tags, labels, marks
- G01N2021/6441—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" with indicators, stains, dyes, tags, labels, marks with two or more labels
- 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
- Y10T436/13—Tracers or tags
- 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
- Y10T436/21—Hydrocarbon

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Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Physics & Mathematics (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Immunology (AREA)
Engineering & Computer Science (AREA)
Biochemistry (AREA)
Analytical Chemistry (AREA)
General Chemical & Material Sciences (AREA)
General Health & Medical Sciences (AREA)
General Physics & Mathematics (AREA)
Pathology (AREA)
Molecular Biology (AREA)
Organic Chemistry (AREA)
Optics & Photonics (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Medicinal Chemistry (AREA)
Food Science & Technology (AREA)
Inks, Pencil-Leads, Or Crayons (AREA)
Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Investigating Or Analysing Materials By Optical Means (AREA)
Optical Record Carriers And Manufacture Thereof (AREA)
Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
Analysing Materials By The Use Of Radiation (AREA)
Ink Jet Recording Methods And Recording Media Thereof (AREA)
Detergent Compositions (AREA)
Paints Or Removers (AREA)

IL13884599A 1998-04-23 1999-04-12 A method of marking liquids with at least two markers and a method of identification IL138845A (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE19818176A DE19818176A1 (de)	1998-04-23	1998-04-23	Verfahren zur Markierung von Flüssigkeiten mit mindestens zwei Markierstoffen und Verfahren zu deren Detektion
PCT/EP1999/002451 WO1999056125A1 (de)	1998-04-23	1999-04-12	Verfahren zur markierung von flüssigkeiten mit mindestens zwei markierstoffen und verfahren zu deren detektion

Publications (2)

Publication Number	Publication Date
IL138845A0 IL138845A0 (en)	2001-10-31
IL138845A true IL138845A (en)	2004-06-20

Family

ID=7865573

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL13884599A IL138845A (en)	1998-04-23	1999-04-12	A method of marking liquids with at least two markers and a method of identification

Country Status (33)

Country	Link
US (1)	US6312958B1 (pt)
EP (1)	EP1082610B1 (pt)
JP (1)	JP4316804B2 (pt)
KR (1)	KR100609673B1 (pt)
CN (1)	CN1145794C (pt)
AR (1)	AR015278A1 (pt)
AT (1)	ATE373822T1 (pt)
AU (1)	AU754193B2 (pt)
BG (1)	BG65287B1 (pt)
BR (1)	BR9909817B1 (pt)
CA (1)	CA2329221C (pt)
CO (1)	CO5090894A1 (pt)
CZ (1)	CZ300963B6 (pt)
DE (2)	DE19818176A1 (pt)
EA (1)	EA002413B1 (pt)
EE (1)	EE04508B1 (pt)
ES (1)	ES2293723T3 (pt)
GE (1)	GEP20033105B (pt)
HU (1)	HUP0102734A3 (pt)
IL (1)	IL138845A (pt)
MX (1)	MXPA00009804A (pt)
MY (1)	MY121841A (pt)
NO (1)	NO20005280L (pt)
NZ (1)	NZ508195A (pt)
PE (1)	PE20000447A1 (pt)
PL (1)	PL193266B1 (pt)
PT (1)	PT1082610E (pt)
SK (1)	SK286179B6 (pt)
TR (1)	TR200003066T2 (pt)
TW (1)	TW503315B (pt)
UA (1)	UA66381C2 (pt)
WO (1)	WO1999056125A1 (pt)
ZA (1)	ZA200006828B (pt)

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1998
- 1998-04-23 DE DE19818176A patent/DE19818176A1/de not_active Withdrawn
1999
- 1999-04-12 NZ NZ508195A patent/NZ508195A/en unknown
- 1999-04-12 JP JP2000546235A patent/JP4316804B2/ja not_active Expired - Fee Related
- 1999-04-12 AT AT99920643T patent/ATE373822T1/de not_active IP Right Cessation
- 1999-04-12 BR BRPI9909817-2A patent/BR9909817B1/pt not_active IP Right Cessation
- 1999-04-12 AU AU38152/99A patent/AU754193B2/en not_active Ceased
- 1999-04-12 EA EA200001093A patent/EA002413B1/ru not_active IP Right Cessation
- 1999-04-12 CA CA002329221A patent/CA2329221C/en not_active Expired - Fee Related
- 1999-04-12 EE EEP200000612A patent/EE04508B1/xx not_active IP Right Cessation
- 1999-04-12 GE GEAP19995641A patent/GEP20033105B/en unknown
- 1999-04-12 WO PCT/EP1999/002451 patent/WO1999056125A1/de active IP Right Grant
- 1999-04-12 IL IL13884599A patent/IL138845A/en not_active IP Right Cessation
- 1999-04-12 DE DE59914509T patent/DE59914509D1/de not_active Expired - Lifetime
- 1999-04-12 HU HU0102734A patent/HUP0102734A3/hu unknown
- 1999-04-12 EP EP99920643A patent/EP1082610B1/de not_active Expired - Lifetime
- 1999-04-12 TR TR2000/03066T patent/TR200003066T2/xx unknown
- 1999-04-12 SK SK1486-2000A patent/SK286179B6/sk not_active IP Right Cessation
- 1999-04-12 KR KR1020007011759A patent/KR100609673B1/ko not_active IP Right Cessation
- 1999-04-12 CN CNB998078581A patent/CN1145794C/zh not_active Expired - Fee Related
- 1999-04-12 US US09/673,736 patent/US6312958B1/en not_active Expired - Fee Related
- 1999-04-12 ES ES99920643T patent/ES2293723T3/es not_active Expired - Lifetime
- 1999-04-12 PL PL344017A patent/PL193266B1/pl not_active IP Right Cessation
- 1999-04-12 CZ CZ20003909A patent/CZ300963B6/cs not_active IP Right Cessation
- 1999-04-12 PT PT99920643T patent/PT1082610E/pt unknown
- 1999-04-20 PE PE1999000333A patent/PE20000447A1/es not_active Application Discontinuation
- 1999-04-21 MY MYPI99001566A patent/MY121841A/en unknown
- 1999-04-22 CO CO99024390A patent/CO5090894A1/es unknown
- 1999-04-22 AR ARP990101865A patent/AR015278A1/es active IP Right Grant
- 1999-04-22 TW TW088106444A patent/TW503315B/zh not_active IP Right Cessation
- 1999-12-04 UA UA2000116627A patent/UA66381C2/uk unknown
2000
- 2000-10-06 MX MXPA00009804 patent/MXPA00009804A/es unknown
- 2000-10-20 NO NO20005280A patent/NO20005280L/no not_active Application Discontinuation
- 2000-11-15 BG BG104951A patent/BG65287B1/bg unknown
- 2000-11-22 ZA ZA200006828A patent/ZA200006828B/en unknown

Also Published As

Publication number	Publication date
EE200000612A (et)	2002-04-15
IL138845A0 (en)	2001-10-31
BR9909817A (pt)	2000-12-19
JP2002513155A (ja)	2002-05-08
DE59914509D1 (de)	2007-10-31
TR200003066T2 (tr)	2001-01-22
NZ508195A (en)	2002-07-26
PL193266B1 (pl)	2007-01-31
KR100609673B1 (ko)	2006-08-09
BG65287B1 (bg)	2007-11-30
BG104951A (en)	2001-05-31
NO20005280D0 (no)	2000-10-20
AU3815299A (en)	1999-11-16
ES2293723T3 (es)	2008-03-16
EE04508B1 (et)	2005-06-15
UA66381C2 (en)	2004-05-17
JP4316804B2 (ja)	2009-08-19
MY121841A (en)	2006-02-28
DE19818176A1 (de)	1999-10-28
KR20010042936A (ko)	2001-05-25
BR9909817B1 (pt)	2010-11-30
PE20000447A1 (es)	2000-05-23
GEP20033105B (en)	2003-10-27
CO5090894A1 (es)	2001-10-30
ZA200006828B (en)	2001-11-22
CA2329221C (en)	2009-12-22
EA002413B1 (ru)	2002-04-25
US6312958B1 (en)	2001-11-06
AR015278A1 (es)	2001-04-18
TW503315B (en)	2002-09-21
PL344017A1 (en)	2001-09-24
EP1082610B1 (de)	2007-09-19
ATE373822T1 (de)	2007-10-15
HUP0102734A3 (en)	2004-10-28
NO20005280L (no)	2000-12-19
CN1145794C (zh)	2004-04-14
CN1307680A (zh)	2001-08-08
SK14862000A3 (sk)	2001-06-11
PT1082610E (pt)	2007-10-25
EP1082610A1 (de)	2001-03-14
SK286179B6 (sk)	2008-04-07
MX213588B (pt)	2003-04-08
CA2329221A1 (en)	1999-11-04
HUP0102734A2 (hu)	2001-12-28
CZ300963B6 (cs)	2009-09-23
EA200001093A1 (ru)	2001-04-23
MXPA00009804A (es)	2001-03-31
AU754193B2 (en)	2002-11-07
WO1999056125A1 (de)	1999-11-04
CZ20003909A3 (cs)	2001-10-17

Legal Events

Date	Code	Title
2004-11-24	FF	Patent granted
2005-06-19	KB	Patent renewed
2009-09-15	KB	Patent renewed
2013-11-28	MM9K	Patent not in force due to non-payment of renewal fees

Publication	Publication Date	Title
CA2329221C (en)	2009-12-22	Method for marking liquids with at least two marker substances and method for detecting them
US5804447A (en)	1998-09-08	Use of compounds which absorb and/or fluoresce in the IR region as markers for liquids
CA2140667C (en)	2003-09-23	Use of compounds which absorb and/or fluoresce in the i/r range as markers for liquids
US5723338A (en)	1998-03-03	Tagging hydrocarbons for subsequent identification
US5710046A (en)	1998-01-20	Tagging hydrocarbons for subsequent identification
US20080190354A1 (en)	2008-08-14	Detection system
PT1266446E (pt)	2007-10-25	Gerador síncrono
US5843783A (en)	1998-12-01	Tagging hydrocarbons for subsequent identification
PT1310585E (pt)	2007-10-25	Aparelho e processo para extrução por fusão
DE19818177A1 (de)	1999-10-28	Verfahren zur Markierung von Flüssigkeiten mit mindestens zwei Markierstoffen und Verfahren zu deren Detektion
Kozlov et al.	2000	Spectral instruments for studying oil and petroleum products