KR102166437B1 - 카바메이트기를 포함하는 아민계 유류식별제 및 이를 이용한 유류식별방법 - Google Patents
카바메이트기를 포함하는 아민계 유류식별제 및 이를 이용한 유류식별방법 Download PDFInfo
- Publication number
- KR102166437B1 KR102166437B1 KR1020140006987A KR20140006987A KR102166437B1 KR 102166437 B1 KR102166437 B1 KR 102166437B1 KR 1020140006987 A KR1020140006987 A KR 1020140006987A KR 20140006987 A KR20140006987 A KR 20140006987A KR 102166437 B1 KR102166437 B1 KR 102166437B1
- Authority
- KR
- South Korea
- Prior art keywords
- oil
- marker
- acid
- butyl
- carbamate
- 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.)
- Active
Links
- 239000003550 marker Substances 0.000 title claims abstract description 70
- 238000000034 method Methods 0.000 title claims abstract description 54
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical group NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 title claims abstract description 44
- 239000003208 petroleum Substances 0.000 title description 7
- 150000001412 amines Chemical class 0.000 claims abstract description 32
- 238000002835 absorbance Methods 0.000 claims abstract description 22
- 239000003921 oil Substances 0.000 claims description 111
- FEMOMIGRRWSMCU-UHFFFAOYSA-N ninhydrin Chemical compound C1=CC=C2C(=O)C(O)(O)C(=O)C2=C1 FEMOMIGRRWSMCU-UHFFFAOYSA-N 0.000 claims description 37
- 239000003795 chemical substances by application Substances 0.000 claims description 20
- 239000003153 chemical reaction reagent Substances 0.000 claims description 13
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 claims description 12
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 11
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 10
- -1 tert-butyl-N-(4-{[(tert-butoxy)carbonyl](methyl) Amino}butyl)-N-methylcarbamate (tert-butyl-N-(4-{[(tert-butoxy)carbonyl](methyl)amino}butyl)-N-methylcarbamate) Chemical compound 0.000 claims description 10
- 239000003350 kerosene Substances 0.000 claims description 9
- 229910052698 phosphorus Inorganic materials 0.000 claims description 9
- 229910052717 sulfur Inorganic materials 0.000 claims description 9
- 238000010306 acid treatment Methods 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 8
- 229910052736 halogen Inorganic materials 0.000 claims description 8
- 150000002367 halogens Chemical class 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- 239000003054 catalyst Substances 0.000 claims description 6
- 150000007522 mineralic acids Chemical class 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- 150000007524 organic acids Chemical class 0.000 claims description 5
- 229910052723 transition metal Inorganic materials 0.000 claims description 5
- 150000003624 transition metals Chemical class 0.000 claims description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims description 4
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 4
- 239000003502 gasoline Substances 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 3
- 238000002203 pretreatment Methods 0.000 claims description 3
- MXSNQMUVXLVDHI-UHFFFAOYSA-N tert-butyl n-butylcarbamate Chemical compound CCCCNC(=O)OC(C)(C)C MXSNQMUVXLVDHI-UHFFFAOYSA-N 0.000 claims description 3
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 2
- 238000010521 absorption reaction Methods 0.000 claims description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- 239000002199 base oil Substances 0.000 claims description 2
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 claims description 2
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 claims description 2
- 229910000042 hydrogen bromide Inorganic materials 0.000 claims description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 2
- 229910000043 hydrogen iodide Inorganic materials 0.000 claims description 2
- 239000010687 lubricating oil Substances 0.000 claims description 2
- 229940098779 methanesulfonic acid Drugs 0.000 claims description 2
- 239000002480 mineral oil Substances 0.000 claims description 2
- 235000010446 mineral oil Nutrition 0.000 claims description 2
- 229910017604 nitric acid Inorganic materials 0.000 claims description 2
- 238000000870 ultraviolet spectroscopy Methods 0.000 claims description 2
- 150000002431 hydrogen Chemical group 0.000 claims 2
- OWOZLAYXMYQYNC-UHFFFAOYSA-N tert-butyl n-[4-[(2-methylpropan-2-yl)oxycarbonylamino]butyl]carbamate Chemical compound CC(C)(C)OC(=O)NCCCCNC(=O)OC(C)(C)C OWOZLAYXMYQYNC-UHFFFAOYSA-N 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 abstract description 24
- 238000011161 development Methods 0.000 abstract description 14
- 239000003463 adsorbent Substances 0.000 abstract description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 19
- 230000018109 developmental process Effects 0.000 description 13
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 125000005842 heteroatom Chemical group 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 5
- 230000008859 change Effects 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 4
- 150000003973 alkyl amines Chemical class 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 4
- 230000001939 inductive effect Effects 0.000 description 4
- 230000003472 neutralizing effect Effects 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 150000004985 diamines Chemical class 0.000 description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- 238000001179 sorption measurement Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000002372 labelling Methods 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 239000003209 petroleum derivative Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 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
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ZAWMUPTUBHPLTI-UHFFFAOYSA-N C1(=C(C=CC=C1)N(C(OC(C)(C)C)=O)C)N(C(OC(C)(C)C)=O)C Chemical compound C1(=C(C=CC=C1)N(C(OC(C)(C)C)=O)C)N(C(OC(C)(C)C)=O)C ZAWMUPTUBHPLTI-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- VQJDBGSINGXXEB-UHFFFAOYSA-N benzyl n-butylcarbamate Chemical compound CCCCNC(=O)OCC1=CC=CC=C1 VQJDBGSINGXXEB-UHFFFAOYSA-N 0.000 description 1
- NDKBVBUGCNGSJJ-UHFFFAOYSA-M benzyltrimethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)CC1=CC=CC=C1 NDKBVBUGCNGSJJ-UHFFFAOYSA-M 0.000 description 1
- ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 238000010511 deprotection reaction Methods 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 239000012954 diazonium Substances 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-O diazynium Chemical compound [NH+]#N IJGRMHOSHXDMSA-UHFFFAOYSA-O 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000005504 petroleum refining Methods 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- BDJXVNRFAQSMAA-UHFFFAOYSA-N quinhydrone Chemical compound OC1=CC=C(O)C=C1.O=C1C=CC(=O)C=C1 BDJXVNRFAQSMAA-UHFFFAOYSA-N 0.000 description 1
- 229940052881 quinhydrone Drugs 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- SBFXRAQMZINCEI-UHFFFAOYSA-N tert-butyl N-methyl-N-[4-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]butyl]carbamate Chemical compound C(CCCN(C(OC(C)(C)C)=O)C)N(C(OC(C)(C)C)=O)C SBFXRAQMZINCEI-UHFFFAOYSA-N 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N31/00—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods
- G01N31/22—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods using chemical indicators
-
- 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
- G01N21/31—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
- G01N21/33—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using ultraviolet light
-
- 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
- G01N21/75—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
- G01N21/77—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator
-
- 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
- G01N33/22—Fuels; Explosives
-
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Food Science & Technology (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Plasma & Fusion (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
Abstract
본 발명은 흡착제에 의해 쉽게 제거되지 아니하며, 반응속도가 빠르고, 재현성이 우수한 카바메이트기를 포함하는 아민계 유류 식별제(Marker) 및 이를 이용한 유류식별방법을 제공할 수 있다.
Description
Claims (13)
- 제 1항에 있어서,
상기 화학식 (1)은 터트-뷰틸-N-뷰틸카바메이트(tert-butyl-N-butylcarbamate), 터트-뷰틸-N-(4-{[(터트-뷰톡시)카보닐]아미노}뷰틸)카바메이트( tert-butyl-N-(4-{[(tert-butoxy)carbonyl]amino}butyl)carbamate), 터트-뷰틸-N-(4-{[(터트-뷰톡시)카보닐](메틸)아미노}뷰틸)-N-메틸카바메이트(tert-butyl-N-(4-{[(tert-butoxy)carbonyl](methyl)amino}butyl)-N-methylcarbamate), 9H-플루오렌-9-일메틸-N-뷰틸카바메이트(9H-fluoren-9-ylmethyl-N-butylcarbamate), 프로프-2-엔-1-일-N-뷰틸카바메이트(Prop-2-en-1-yl-N-butylcarbamate), 뷰틸-N-(2,2,2,-트리클로로에틸)카바메이트(Butyl-N-(2,2,2,-trichloroethyl)carbamate), 9H-플루오렌-9-일메틸-N-(2-{[(9H-fluoren-9-일메톡시)카보닐]아미노}에틸)카바메이트(9H-fluoren-9-ylmethyl-N-(2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}ethyl)carbamate) 중에서 선택되는 어느 하나인 카바메이트기를 포함하는 아민계 유류 식별제(Marker).
- 제 1항의 상기 화학식 (1)의 카바메이트기를 포함하는 아민계 유류 식별제(Marker)로 표지된 유류를 전처리 하는 단계; 및
상기 전처리된 유류 식별제(Marker)를 닌하이드린과 반응시키는 단계;를 포함하는 유류식별방법. - 제 4항에 있어서,
상기 전처리는 산처리, 염기처리 및 전이금속 촉매를 이용한 처리 중 선택되는 어느 하나를 포함하는 것인 유류식별방법. - 제 5항에 있어서,
상기 산처리 단계는 유기산 또는 무기산으로 산처리 하는 것인 유류식별방법. - 제 6항에 있어서,
상기 유기산 또는 무기산은 황산, 트리플루오르아세트산, 염산, 브롬화수소, 요오드화 수소, 질산, 인산, 크롬산, 메탄술폰산 중 선택되는 어느 하나 또는 이들의 혼합물 인 것을 특징으로 하는 유류식별방법. - 제 3항 내지 제 7항 중 어느 하나의 항에 있어서,
흡광도 측정장치를 이용하여 흡광도를 측정하는 단계;를 더 포함하는 유류 식별방법. - 제 8항에 있어서,
상기 유류식별제가 상기 유류 내 1 내지 800ppm 포함되어 있는 것을 특징으로 하는 유류 식별방법. - 제 9항에 있어서,
상기 유류가 광유, 기유, 등유, 윤활유, 휘발유 중에서 선택되는 어느 하나인 유류 식별방법. - 제 10항에 있어서,
상기 흡광도 측정장치를 이용하여 측정한 흡광도의 최대흡수 파장이 400 내지 800nm인 유류 식별방법. - 제 11항에 있어서,
상기 흡광도 측정장치는 이동성 자외선 가시분광 광도계인 것을 특징으로 하는 유류 식별방법.
- 제 1항에 있어서,
상기 유류 식별제를 이용하여 전개시약인 닌하이드린과 반응시켜 발색하게 하는 것을 특징으로 하는, 아민계 유류 식별제(Marker).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020140006987A KR102166437B1 (ko) | 2014-01-21 | 2014-01-21 | 카바메이트기를 포함하는 아민계 유류식별제 및 이를 이용한 유류식별방법 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020140006987A KR102166437B1 (ko) | 2014-01-21 | 2014-01-21 | 카바메이트기를 포함하는 아민계 유류식별제 및 이를 이용한 유류식별방법 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20150086859A KR20150086859A (ko) | 2015-07-29 |
KR102166437B1 true KR102166437B1 (ko) | 2020-10-15 |
Family
ID=53876304
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020140006987A Active KR102166437B1 (ko) | 2014-01-21 | 2014-01-21 | 카바메이트기를 포함하는 아민계 유류식별제 및 이를 이용한 유류식별방법 |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR102166437B1 (ko) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009120563A1 (en) | 2008-03-25 | 2009-10-01 | The Lubrizol Corporation | Marker dyes for petroleum products |
KR100953358B1 (ko) | 2008-10-14 | 2010-04-20 | 오리엔트화학 (주) | 금속 착염 발색제를 이용하여 발색되는 유류 식별용 마커, 상기 마커를 이용하는 유류 식별 방법 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS602056B2 (ja) | 1979-10-11 | 1985-01-18 | 株式会社千代田製作所 | 医療用器具ガス滅菌容器のガス除去方法及びその装置 |
DE4238994A1 (de) * | 1992-11-19 | 1994-05-26 | Basf Ag | Aniline als Markierungsmittel für Mineralöle |
KR20030040312A (ko) * | 2003-04-24 | 2003-05-22 | (주)이노바이오시스템 | 염료를 이용한 유사휘발유 검지스트립 및 이를 이용한 시료측정 방법 |
KR101058120B1 (ko) | 2009-10-09 | 2011-08-24 | 오리엔트화학 (주) | 석유 제품의 식별방법 및 이에 사용되는 석유 제품용 식별제 |
-
2014
- 2014-01-21 KR KR1020140006987A patent/KR102166437B1/ko active Active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009120563A1 (en) | 2008-03-25 | 2009-10-01 | The Lubrizol Corporation | Marker dyes for petroleum products |
KR100953358B1 (ko) | 2008-10-14 | 2010-04-20 | 오리엔트화학 (주) | 금속 착염 발색제를 이용하여 발색되는 유류 식별용 마커, 상기 마커를 이용하는 유류 식별 방법 |
Also Published As
Publication number | Publication date |
---|---|
KR20150086859A (ko) | 2015-07-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Ponnuvel et al. | Highly efficient and selective detection of picric acid among other nitroaromatics by NIR fluorescent organic fluorophores | |
Tang et al. | Rapid and highly selective relay recognition of Cu (II) and sulfide ions by a simple benzimidazole-based fluorescent sensor in water | |
US4209302A (en) | Marker for petroleum fuels | |
Min et al. | Rhodamine-fluorene based dual channel probe for the detection of Hg2+ ions and its application in digital printing | |
Wang et al. | Highly Selective Turn‐On Fluorescent Chemodosimeter for AlIII Detection through AlIII‐Promoted Hydrolysis of C= N Double Bonds in the 8‐Hydroxyquinoline Aldehyde Schiff Base | |
KR100854158B1 (ko) | 마커를 함유하는 석유 제품의 조성물, 마커, 및 석유 제품의 확인 방법 | |
Zhang et al. | An effective fluorescent probe for detection of phosgene based on naphthalimide dyes in liquid and gaseous phases | |
WO2014087360A1 (en) | Method for detection of kerosene adulteration with extrinsic marker in gasoline, aviation turbine fuel and diesel | |
KR102166437B1 (ko) | 카바메이트기를 포함하는 아민계 유류식별제 및 이를 이용한 유류식별방법 | |
KR101058120B1 (ko) | 석유 제품의 식별방법 및 이에 사용되는 석유 제품용 식별제 | |
CN109824682B (zh) | 一种基于罗丹明b酰肼的汞离子传感器分子及其制备和应用 | |
EP3183561A1 (en) | Chemical probes for hydrogen sulfide | |
KR20020024783A (ko) | 무색 석유 표지물 염료 | |
US20170175017A1 (en) | Method of making hydrocarbon liquids | |
CN102268249A (zh) | 一种可用肉眼检测汞离子的荧光探针及其制备方法和应用 | |
KR102027114B1 (ko) | 신규 유류식별제 및 이를 이용한 유류식별방법 | |
Zhou et al. | Nucleophilic Addition‐Triggered Lanthanide Luminescence Allows Detection of Amines by Eu (thenoyltrifluoroacetone) 3 | |
JP6374538B2 (ja) | 石油製品の識別方法及び石油製品識別用組成物 | |
EP2881455B1 (en) | Diamine-based oil marker compositions and method of identifying oil product using the same | |
KR102303537B1 (ko) | 디아민계 유류 식별제(Marker) 및 이를 이용한 유류식별방법 | |
Ghosh et al. | Rhodamine‐labeled Sensor Bead as a Colorimetric and Fluorometric Dual Assay for Hg2+ Ions in Water | |
KR100779057B1 (ko) | 석유 제품용 식별제를 프탈레인 유도체의 알킬산 현탁액에티오닐 클로라이드를 반응물질로 한 에스테르 제조방법 | |
US20220298439A1 (en) | Tracers and method of marking liquids | |
Maiti et al. | An Adenine‐Based Chromone‐Coupled ‘Off‐On‐Off’Fluorogenic Dyad for Cascade Detection of Zn2+ and HSO₄− Ions or Zn2+ Ions and Picric Acid | |
EP2738154A1 (en) | Improved fuel markers |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 20140121 |
|
PG1501 | Laying open of application | ||
PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 20181227 Comment text: Request for Examination of Application Patent event code: PA02011R01I Patent event date: 20140121 Comment text: Patent Application |
|
E902 | Notification of reason for refusal | ||
PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20200306 Patent event code: PE09021S01D |
|
E701 | Decision to grant or registration of patent right | ||
PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 20200929 |
|
PR0701 | Registration of establishment |
Comment text: Registration of Establishment Patent event date: 20201008 Patent event code: PR07011E01D |
|
PR1002 | Payment of registration fee |
Payment date: 20201012 End annual number: 3 Start annual number: 1 |
|
PG1601 | Publication of registration | ||
PR1001 | Payment of annual fee |
Payment date: 20230912 Start annual number: 4 End annual number: 4 |
|
PR1001 | Payment of annual fee |
Payment date: 20240927 Start annual number: 5 End annual number: 5 |