KR100914259B1 - 금속 착염 발색제를 이용하여 발색되는 유류 식별용 마커, 상기 마커를 이용하는 유류 식별 방법 - Google Patents
금속 착염 발색제를 이용하여 발색되는 유류 식별용 마커, 상기 마커를 이용하는 유류 식별 방법 Download PDFInfo
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- KR100914259B1 KR100914259B1 KR1020080127074A KR20080127074A KR100914259B1 KR 100914259 B1 KR100914259 B1 KR 100914259B1 KR 1020080127074 A KR1020080127074 A KR 1020080127074A KR 20080127074 A KR20080127074 A KR 20080127074A KR 100914259 B1 KR100914259 B1 KR 100914259B1
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- 239000003550 marker Substances 0.000 title claims abstract description 26
- 238000000034 method Methods 0.000 title claims abstract description 9
- -1 metal complex salts Chemical class 0.000 title description 8
- 150000001875 compounds Chemical class 0.000 claims abstract description 33
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 23
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 14
- 125000003118 aryl group Chemical group 0.000 claims abstract description 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 10
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 8
- 125000005843 halogen group Chemical group 0.000 claims abstract description 8
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 6
- 238000002372 labelling Methods 0.000 claims abstract description 4
- 125000003107 substituted aryl group Chemical group 0.000 claims abstract 2
- 239000003086 colorant Substances 0.000 claims description 14
- 229910021645 metal ion Inorganic materials 0.000 claims description 9
- 125000001033 ether group Chemical group 0.000 claims description 7
- 125000001424 substituent group Chemical group 0.000 claims description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 239000000126 substance Substances 0.000 abstract description 8
- 125000003277 amino group Chemical group 0.000 abstract description 2
- 239000003921 oil Substances 0.000 description 22
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 19
- 239000001301 oxygen Substances 0.000 description 19
- 239000000446 fuel Substances 0.000 description 14
- 239000002904 solvent Substances 0.000 description 13
- 125000000686 lactone group Chemical group 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 4
- 125000004185 ester group Chemical group 0.000 description 4
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 4
- 239000003208 petroleum Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000000010 aprotic solvent Substances 0.000 description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
- 239000003849 aromatic solvent Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 239000010687 lubricating oil Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000009965 odorless effect Effects 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- PBRXKNKPUMMYPO-UHFFFAOYSA-N 1-$l^{1}-oxidanyl-2-methylpropane Chemical compound CC(C)C[O] PBRXKNKPUMMYPO-UHFFFAOYSA-N 0.000 description 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- MFGZXPGKKJMZIY-UHFFFAOYSA-N ethyl 5-amino-1-(4-sulfamoylphenyl)pyrazole-4-carboxylate Chemical compound NC1=C(C(=O)OCC)C=NN1C1=CC=C(S(N)(=O)=O)C=C1 MFGZXPGKKJMZIY-UHFFFAOYSA-N 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000434 metal complex dye Substances 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- DVQHRBFGRZHMSR-UHFFFAOYSA-N sodium methyl 2,2-dimethyl-4,6-dioxo-5-(N-prop-2-enoxy-C-propylcarbonimidoyl)cyclohexane-1-carboxylate Chemical compound [Na+].C=CCON=C(CCC)[C-]1C(=O)CC(C)(C)C(C(=O)OC)C1=O DVQHRBFGRZHMSR-UHFFFAOYSA-N 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000002211 ultraviolet spectrum Methods 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/10—Spiro-condensed systems
-
- 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
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
-
- 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
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Analytical Chemistry (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Food Science & Technology (AREA)
- Medicinal Chemistry (AREA)
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
Abstract
Description
R 1 | R 2 | R 3 | R 4 | R 5 | X | |
구조 1 | C2H5 | C2H5 | 벤질 | 벤질 | H | 산소(O) |
구조 2 | C4H9 | C4H9 | H | o-클로로페닐 | H | 산소(O) |
구조 3 | C4H9 | C4H9 | H | 페닐 | CH3 | 산소(O) |
구조 4 | C2H5 | C2H5 | H | m-트리플루오로메틸 페닐 | H | 산소(O) |
구조 5 | C2H5 | C2H5 | H | p-부틸 페닐 | CH3 | 산소(O) |
구조 6 | C2H5 | C2H5 | H | 페닐 | Cl | 산소(O) |
구조 7 | C2H5 | C2H5 | H | 페닐 | H | 산소(O) |
구조 8 | C2H5 | C2H5 | H | CH3 | H | 산소(O) |
구조 9 | C2H5 | C2H5 | CH3 | CH3 | C2H5 | 산소(O) |
구조 10 | H | H | C2H5 | C2H5 | C2H5 | 산소(O) |
구조 11 | C3H7 | C3H7 | C3H7 | C3H7 | C3H7 | 산소(O) |
구조 12 | C4H9 | C4H9 | C4H9 | C4H9 | C4H9 | 산소(O) |
구조 13 | C5H11 | C5H11 | C5H11 | C5H11 | C5H11 | 산소(O) |
구조 14 | C5H11 | C5H11 | C5H11 | C5H11 | H | 산소(O) |
구조 15 | H | H | C5H11 | C5H11 | C5H11 | 산소(O) |
구조 16 | 이소-부틸 | 이소-부틸 | 이소-부틸 | 이소-부틸 | 이소-부틸 | 산소(O) |
구조 17 | C6H13 | C6H13 | C6H13 | C6H13 | C6H13 | 산소(O) |
구조 18 | CnHm | CnHm | CnHm | CnHm | CnHm | 산소(O) |
구조 19 | A | A | A | A | A | 산소(O) |
구조 20 | A | A | CnHm | CnHm | A | 산소(O) |
구조 21~40 | 황(S) |
Claims (7)
- 삭제
- 삭제
- 삭제
- 삭제
- 삭제
- 하기 화학식 1의 화합물을 포함하는 식별용 마커를 포함시켜서 유류 제품을 표지하고, 하기 화학식 2의 화합물을 포함하는 발색제를 첨가하는 단계를 포함하는 유류 식별 방법.[화학식 1](상기 식에서 X는 O 또는 S이고, R1~R5는 각각 독립적으로 수소원자, 할로겐원자, 또는 1 내지 12 개의 탄소 원자를 갖는 직쇄 또는 분지쇄 알킬 기, 벤질기, 치환 또는 미치환된 아릴기를 나타내며, 상기 치환된 아릴기에서 치환기는 1 내지 12 개의 탄소 원자를 갖는 직쇄 또는 분지쇄 알킬 기, 할로겐, 또는 1 내지 12 개의 탄소 원자를 갖는 할로 알킬 기이다.)[화학식 2](상기 식에서 금속이온(Metal ++)은 2가 금속 이온을 나타내고; X1, X2는 각각 독립적으로 수소원자, 알킬 기 또는 카르보닐 기를 나타내며; R1, R2는 각각 독립적으로 수소원자, 할로겐원자, 벤질기 또는 1 내지 10개의 탄소원자를 갖는 알킬 기 또는 1 내지 10개의 탄소원자를 갖는 에테르 기를 나타낸다.)
- 삭제
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KR1020080127074A KR100914259B1 (ko) | 2008-12-15 | 2008-12-15 | 금속 착염 발색제를 이용하여 발색되는 유류 식별용 마커, 상기 마커를 이용하는 유류 식별 방법 |
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KR1020080127074A KR100914259B1 (ko) | 2008-12-15 | 2008-12-15 | 금속 착염 발색제를 이용하여 발색되는 유류 식별용 마커, 상기 마커를 이용하는 유류 식별 방법 |
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KR100914259B1 true KR100914259B1 (ko) | 2009-08-27 |
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KR1020080127074A KR100914259B1 (ko) | 2008-12-15 | 2008-12-15 | 금속 착염 발색제를 이용하여 발색되는 유류 식별용 마커, 상기 마커를 이용하는 유류 식별 방법 |
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01104692A (ja) * | 1987-09-18 | 1989-04-21 | Basf Ag | 標識された鉱油製品及びその製法 |
KR20020033033A (ko) * | 2001-06-13 | 2002-05-04 | 이인남 | 석유 제품용 식별제, 이를 이용한 석유제품의 표지 및검출방법 |
US20080196177A1 (en) * | 2007-02-09 | 2008-08-21 | Moore Patrick D | Unsubstituted and polymeric fluoran colorants for coloring consumer products |
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- 2008-12-15 KR KR1020080127074A patent/KR100914259B1/ko active IP Right Grant
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01104692A (ja) * | 1987-09-18 | 1989-04-21 | Basf Ag | 標識された鉱油製品及びその製法 |
KR20020033033A (ko) * | 2001-06-13 | 2002-05-04 | 이인남 | 석유 제품용 식별제, 이를 이용한 석유제품의 표지 및검출방법 |
US20080196177A1 (en) * | 2007-02-09 | 2008-08-21 | Moore Patrick D | Unsubstituted and polymeric fluoran colorants for coloring consumer products |
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