TW201219555A - promoting the Brownian motion by the addition of a sublimatable organic compound - Google Patents
promoting the Brownian motion by the addition of a sublimatable organic compound Download PDFInfo
- Publication number
- TW201219555A TW201219555A TW099138652A TW99138652A TW201219555A TW 201219555 A TW201219555 A TW 201219555A TW 099138652 A TW099138652 A TW 099138652A TW 99138652 A TW99138652 A TW 99138652A TW 201219555 A TW201219555 A TW 201219555A
- Authority
- TW
- Taiwan
- Prior art keywords
- hydroxy
- isobutyl
- methyl
- isopropyl
- organic compound
- Prior art date
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- 150000002894 organic compounds Chemical class 0.000 title claims abstract description 51
- 230000005653 Brownian motion process Effects 0.000 title abstract description 3
- 238000005537 brownian motion Methods 0.000 title abstract description 3
- 230000001737 promoting effect Effects 0.000 title 1
- 239000000446 fuel Substances 0.000 claims abstract description 50
- 239000000654 additive Substances 0.000 claims abstract description 39
- 230000000996 additive effect Effects 0.000 claims abstract description 39
- 239000007788 liquid Substances 0.000 claims abstract description 38
- 238000002485 combustion reaction Methods 0.000 claims abstract description 18
- 238000000034 method Methods 0.000 claims abstract description 16
- 239000007787 solid Substances 0.000 claims abstract description 7
- -1 methyl dihydrogen Chemical compound 0.000 claims description 47
- 239000003502 gasoline Substances 0.000 claims description 36
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 14
- XPCTZQVDEJYUGT-UHFFFAOYSA-N 3-hydroxy-2-methyl-4-pyrone Chemical compound CC=1OC=CC(=O)C=1O XPCTZQVDEJYUGT-UHFFFAOYSA-N 0.000 claims description 10
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 9
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 claims description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 9
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 claims description 8
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 claims description 8
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 8
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 claims description 8
- 229940041616 menthol Drugs 0.000 claims description 8
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexyloxide Natural products O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims description 6
- 238000000859 sublimation Methods 0.000 claims description 6
- 230000008022 sublimation Effects 0.000 claims description 6
- ZTSXWRXRDAAGPA-UHFFFAOYSA-N 1-methyl-2,5-bis(2-methylpropyl)-4-propan-2-ylbenzene Chemical compound CC(C)Cc1cc(C(C)C)c(CC(C)C)cc1C ZTSXWRXRDAAGPA-UHFFFAOYSA-N 0.000 claims description 5
- FDZSOJOJVCBNNI-UHFFFAOYSA-N 1-tert-butylcyclohexan-1-ol Chemical compound CC(C)(C)C1(O)CCCCC1 FDZSOJOJVCBNNI-UHFFFAOYSA-N 0.000 claims description 5
- JUPQMUMLTZVJRN-UHFFFAOYSA-N 2-ethyl-4-(2-methylpropyl)cyclobutan-1-ol Chemical compound CCC1CC(CC(C)C)C1O JUPQMUMLTZVJRN-UHFFFAOYSA-N 0.000 claims description 5
- FFROMNOQCNVNIH-UHFFFAOYSA-N 2-methylpropylcyclohexane Chemical compound CC(C)CC1CCCCC1 FFROMNOQCNVNIH-UHFFFAOYSA-N 0.000 claims description 5
- HYMLWHLQFGRFIY-UHFFFAOYSA-N Maltol Natural products CC1OC=CC(=O)C1=O HYMLWHLQFGRFIY-UHFFFAOYSA-N 0.000 claims description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 5
- 229940043353 maltol Drugs 0.000 claims description 5
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 claims description 5
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 claims description 4
- UCDKURUNTQPXSD-UHFFFAOYSA-N 2-(2-methylpropyl)-3-propan-2-ylcyclopropan-1-ol Chemical compound CC(C)CC1C(O)C1C(C)C UCDKURUNTQPXSD-UHFFFAOYSA-N 0.000 claims description 4
- DZRLNYVDCIYXPG-UHFFFAOYSA-N 2-naphthalen-2-yloxynaphthalene Chemical compound C1=CC=CC2=CC(OC=3C=C4C=CC=CC4=CC=3)=CC=C21 DZRLNYVDCIYXPG-UHFFFAOYSA-N 0.000 claims description 4
- SDJUYPUXVFDUFF-UHFFFAOYSA-N 2-propan-2-ylcyclohexan-1-one Chemical compound CC(C)C1CCCCC1=O SDJUYPUXVFDUFF-UHFFFAOYSA-N 0.000 claims description 4
- 241000723346 Cinnamomum camphora Species 0.000 claims description 4
- 229930008380 camphor Natural products 0.000 claims description 4
- 229960000846 camphor Drugs 0.000 claims description 4
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 claims description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- BJROFNGVAGISIW-UHFFFAOYSA-N 1-(2-methylpropyl)cyclohexan-1-ol Chemical compound CC(C)CC1(O)CCCCC1 BJROFNGVAGISIW-UHFFFAOYSA-N 0.000 claims description 3
- NHIQZMALAYPXDC-UHFFFAOYSA-N 2,5-bis(2-methylpropyl)cyclohexan-1-ol Chemical compound CC(C)CC1CCC(CC(C)C)C(O)C1 NHIQZMALAYPXDC-UHFFFAOYSA-N 0.000 claims description 3
- MQOYCSYFNQIYDD-UHFFFAOYSA-N 2,5-bis(2-methylpropyl)cyclohexane-1,4-diol Chemical compound CC(C)CC1CC(O)C(CC(C)C)CC1O MQOYCSYFNQIYDD-UHFFFAOYSA-N 0.000 claims description 3
- IKYSUHQDDSDEHS-UHFFFAOYSA-N 2-(2-methylpropyl)cyclohexan-1-ol Chemical compound CC(C)CC1CCCCC1O IKYSUHQDDSDEHS-UHFFFAOYSA-N 0.000 claims description 3
- ZPSJGADGUYYRKE-UHFFFAOYSA-N 2H-pyran-2-one Chemical compound O=C1C=CC=CO1 ZPSJGADGUYYRKE-UHFFFAOYSA-N 0.000 claims description 3
- WPEKOMRBMUAYDT-UHFFFAOYSA-N 4-propan-2-ylcycloheptan-1-ol Chemical compound CC(C)C1CCCC(O)CC1 WPEKOMRBMUAYDT-UHFFFAOYSA-N 0.000 claims description 3
- PMPVIKIVABFJJI-UHFFFAOYSA-N Cyclobutane Chemical compound C1CCC1 PMPVIKIVABFJJI-UHFFFAOYSA-N 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- WJTCGQSWYFHTAC-UHFFFAOYSA-N cyclooctane Chemical compound C1CCCCCCC1 WJTCGQSWYFHTAC-UHFFFAOYSA-N 0.000 claims description 3
- 239000004914 cyclooctane Substances 0.000 claims description 3
- 239000000295 fuel oil Substances 0.000 claims description 3
- 229940075566 naphthalene Drugs 0.000 claims description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 claims description 3
- ULJXKUJMXIVDOY-UHFFFAOYSA-N 2-methyl-5-propan-2-ylcyclohexan-1-ol Chemical compound CC(C)C1CCC(C)C(O)C1 ULJXKUJMXIVDOY-UHFFFAOYSA-N 0.000 claims description 2
- LVZWSLJZHVFIQJ-UHFFFAOYSA-N Cyclopropane Chemical compound C1CC1 LVZWSLJZHVFIQJ-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 claims description 2
- 125000002619 bicyclic group Chemical group 0.000 claims description 2
- 239000003225 biodiesel Substances 0.000 claims 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 claims description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims 8
- IXVGVVQGNQZQGD-UHFFFAOYSA-N 2-propan-2-ylcyclohexan-1-ol Chemical compound CC(C)C1CCCCC1O IXVGVVQGNQZQGD-UHFFFAOYSA-N 0.000 claims 4
- HKDSKLVURHPEAP-UHFFFAOYSA-N 3,7-dimethylcyclooctan-1-one Chemical compound CC1CCCC(C)CC(=O)C1 HKDSKLVURHPEAP-UHFFFAOYSA-N 0.000 claims 4
- 239000002028 Biomass Substances 0.000 claims 4
- JARRBLCOBQBDAY-UHFFFAOYSA-N 4-methyl-2-(2-methylpropyl)cyclopentan-1-ol Chemical compound CC(C)CC1CC(C)CC1O JARRBLCOBQBDAY-UHFFFAOYSA-N 0.000 claims 3
- UXKHYNGZHNLMJD-UHFFFAOYSA-N 4-propan-2-ylcycloheptan-1-one Chemical compound CC(C)C1CCCC(=O)CC1 UXKHYNGZHNLMJD-UHFFFAOYSA-N 0.000 claims 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 claims 2
- QXMUYPHHLVIBTB-UHFFFAOYSA-N 1-propan-2-ylcycloheptan-1-ol Chemical compound CC(C)C1(O)CCCCCC1 QXMUYPHHLVIBTB-UHFFFAOYSA-N 0.000 claims 2
- IWFJPNXYGICSKG-UHFFFAOYSA-N 2-(2-methylpropyl)-3-propan-2-ylcyclopropan-1-one Chemical compound CC(C)CC1C(C(C)C)C1=O IWFJPNXYGICSKG-UHFFFAOYSA-N 0.000 claims 2
- HFQTYOGWDNGZMS-UHFFFAOYSA-N 4,7,7-trimethylbicyclo[2.2.1]heptan-2-one Chemical compound C1CC2(C)CC(=O)C1C2(C)C HFQTYOGWDNGZMS-UHFFFAOYSA-N 0.000 claims 2
- OQLZINXFSUDMHM-UHFFFAOYSA-N Acetamidine Chemical compound CC(N)=N OQLZINXFSUDMHM-UHFFFAOYSA-N 0.000 claims 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 claims 2
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- RREVXPPIGSSYLP-UHFFFAOYSA-N 1,7,7-trimethylbicyclo[2.2.1]heptan-4-ol Chemical compound C1CC2(O)CCC1(C)C2(C)C RREVXPPIGSSYLP-UHFFFAOYSA-N 0.000 claims 1
- FHCVFYFOWIAQDU-UHFFFAOYSA-N 1-hexylcyclohexan-1-ol Chemical compound CCCCCCC1(O)CCCCC1 FHCVFYFOWIAQDU-UHFFFAOYSA-N 0.000 claims 1
- OLZFGHOLNXRJEC-UHFFFAOYSA-N 1-methyl-4-propan-2-ylidenecyclohexane Chemical compound CC1CCC(=C(C)C)CC1 OLZFGHOLNXRJEC-UHFFFAOYSA-N 0.000 claims 1
- VOQQZOUURKJXTL-UHFFFAOYSA-N 2-ethyl-4-(2-methylpropyl)cyclobutan-1-one Chemical compound CCC1CC(CC(C)C)C1=O VOQQZOUURKJXTL-UHFFFAOYSA-N 0.000 claims 1
- NABXJCRMBVOBFI-UHFFFAOYSA-N 2-propan-2-ylcycloheptan-1-one Chemical compound CC(C)C1CCCCCC1=O NABXJCRMBVOBFI-UHFFFAOYSA-N 0.000 claims 1
- OCJLPZCBZSCVCO-UHFFFAOYSA-N 2-propylcyclohexan-1-one Chemical compound CCCC1CCCCC1=O OCJLPZCBZSCVCO-UHFFFAOYSA-N 0.000 claims 1
- NXSFBWSPBYOVPW-UHFFFAOYSA-N 4-(2-methylpropyl)cyclohexan-1-ol Chemical compound CC(C)CC1CCC(O)CC1 NXSFBWSPBYOVPW-UHFFFAOYSA-N 0.000 claims 1
- RSXDSYYYAJHFNM-UHFFFAOYSA-N 4-methyl-2-(2-methylpropyl)cyclopentan-1-one Chemical compound CC(C)CC1CC(C)CC1=O RSXDSYYYAJHFNM-UHFFFAOYSA-N 0.000 claims 1
- QGUPBYVADAJUNT-UHFFFAOYSA-N 6-morpholin-4-ium-4-yl-4,4-diphenylheptan-3-one;chloride Chemical compound Cl.C=1C=CC=CC=1C(C=1C=CC=CC=1)(C(=O)CC)CC(C)N1CCOCC1 QGUPBYVADAJUNT-UHFFFAOYSA-N 0.000 claims 1
- KXJVWNBVRRZEHH-UHFFFAOYSA-N 7,7-dimethylbicyclo[2.2.1]heptane-2,3-dione Chemical compound C1CC2C(=O)C(=O)C1C2(C)C KXJVWNBVRRZEHH-UHFFFAOYSA-N 0.000 claims 1
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- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 229910052797 bismuth Inorganic materials 0.000 claims 1
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- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims 1
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- 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 claims 1
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- 238000001792 White test Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 1
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 1
- USMNOWBWPHYOEA-UHFFFAOYSA-N alpha-thujone Natural products CC1C(=O)CC2(C(C)C)C1C2 USMNOWBWPHYOEA-UHFFFAOYSA-N 0.000 description 1
- 230000003444 anaesthetic effect Effects 0.000 description 1
- CKDOCTFBFTVPSN-UHFFFAOYSA-N borneol Natural products C1CC2(C)C(C)CC1C2(C)C CKDOCTFBFTVPSN-UHFFFAOYSA-N 0.000 description 1
- 229930006739 camphene Natural products 0.000 description 1
- ZYPYEBYNXWUCEA-UHFFFAOYSA-N camphenilone Natural products C1CC2C(=O)C(C)(C)C1C2 ZYPYEBYNXWUCEA-UHFFFAOYSA-N 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 229910002090 carbon oxide Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 210000003169 central nervous system Anatomy 0.000 description 1
- 229910000420 cerium oxide Inorganic materials 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- KMPWYEUPVWOPIM-UHFFFAOYSA-N cinchonidine Natural products C1=CC=C2C(C(C3N4CCC(C(C4)C=C)C3)O)=CC=NC2=C1 KMPWYEUPVWOPIM-UHFFFAOYSA-N 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- ARUKYTASOALXFG-UHFFFAOYSA-N cycloheptylcycloheptane Chemical group C1CCCCCC1C1CCCCCC1 ARUKYTASOALXFG-UHFFFAOYSA-N 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- STWFZICHPLEOIC-UHFFFAOYSA-N decylcyclohexane Chemical compound CCCCCCCCCCC1CCCCC1 STWFZICHPLEOIC-UHFFFAOYSA-N 0.000 description 1
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- WHRIKZCFRVTHJH-UHFFFAOYSA-N ethylhydrazine Chemical compound CCNN WHRIKZCFRVTHJH-UHFFFAOYSA-N 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- UIWYJDYFSGRHKR-UHFFFAOYSA-N gadolinium atom Chemical compound [Gd] UIWYJDYFSGRHKR-UHFFFAOYSA-N 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 239000002815 homogeneous catalyst Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- AFFLGGQVNFXPEV-UHFFFAOYSA-N n-decene Natural products CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- KPMKEVXVVHNIEY-UHFFFAOYSA-N norcamphor Chemical compound C1CC2C(=O)CC1C2 KPMKEVXVVHNIEY-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000008816 organ damage Effects 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- 229930007459 p-menth-8-en-3-one Natural products 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229930006968 piperitone Natural products 0.000 description 1
- CHWRSCGUEQEHOH-UHFFFAOYSA-N potassium oxide Chemical compound [O-2].[K+].[K+] CHWRSCGUEQEHOH-UHFFFAOYSA-N 0.000 description 1
- 229910001950 potassium oxide Inorganic materials 0.000 description 1
- CUYJYVAWBJXBIC-UHFFFAOYSA-N propan-2-ylidenecyclohexane Chemical compound CC(C)=C1CCCCC1 CUYJYVAWBJXBIC-UHFFFAOYSA-N 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 238000013102 re-test Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- 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
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/16—Hydrocarbons
- C10L1/1608—Well defined compounds, e.g. hexane, benzene
-
- 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
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/182—Organic compounds containing oxygen containing hydroxy groups; Salts thereof
- C10L1/1822—Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms
- C10L1/1824—Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms mono-hydroxy
-
- 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
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/185—Ethers; Acetals; Ketals; Aldehydes; Ketones
- C10L1/1852—Ethers; Acetals; Ketals; Orthoesters
- C10L1/1855—Cyclic ethers, e.g. epoxides, lactides, lactones
-
- 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
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/185—Ethers; Acetals; Ketals; Aldehydes; Ketones
- C10L1/1857—Aldehydes; Ketones
-
- 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
- C10L10/00—Use of additives to fuels or fires for particular purposes
-
- 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
- C10L2230/00—Function and purpose of a components of a fuel or the composition as a whole
- C10L2230/22—Function and purpose of a components of a fuel or the composition as a whole for improving fuel economy or fuel efficiency
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Combustion & Propulsion (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
201219555 六、發明說明: 【發明所屬之技術領域】 本發明是有關於一種提昇揪植 ^ 汁燃燒效率的添加劑及方法 特別是指一種提昇液態燃料姆燒 邝…現政率的添加劑及方法。 【先前技術】 k著全球能源危機及環境污染等問題日益嚴重, 的解決方案除了尋求替代能 外’更急需尋求提昇 的燃燒效率並降低燃料用詈的古201219555 VI. Description of the Invention: [Technical Field of the Invention] The present invention relates to an additive and method for improving the combustion efficiency of a simmering juice, in particular, an additive and method for increasing the current rate of liquid fuel smoldering. [Prior Art] K. The global energy crisis and environmental pollution are becoming more and more serious. In addition to seeking alternative energy, the solution is more urgent to seek improved combustion efficiency and reduce the use of fuel.
、 利里的方法。現有提昇燃燒效率的 方法相當多樣化,除了從故p 良九,' 裝置的機械結構著手 外,各式燃料添加劑的傕用> sV t 便用也疋各界所知悉的方法。例如 在無鉛汽油中添加4〜1〇 wt%甲基第三丁基醚(Me_ teniary b卿i ether,MEBT),可幫助汽油完全燃燒並減少 :氧化碳的排放量。但甲基第三丁基醚會引起中樞神經中 ,,長期吸入或暴露於存有甲基第三丁基醚的環境下,恐 引起器官病變以及癌症。 中華民國專利公開案第200927912號揭示一種車輛、 軋舶專用的環保省油精。將此種含有能源活化劑及2_甲基-2_丙醇的液態省油精加入油箱内與燃料均勻混合,可以改善 燃料燃燒不完全的情況。此專利所使用的2_甲基_2_丙醇之 毒性及麻醉性較一般醇類高,故此一環保省油精在使用上 仍有傷害人體及環境的疑慮。 中華民國專利公開案第200825163號提供一種利用分. 子震盡原理的省油粉末,此省油粉末具有遠紅外線及負離 子效能,經由奈米技術處理且由氧化鋅、二氧化矽、碳酸 201219555 妈、氧化鎂、氧化鉀、氧化鋁、稀土元素及微量元素所組 成。此種省油粉末由多種固態無機物所組成,且須經過奈 米技術處理,除了製程上較為繁雜之外,更可能產生與燃 料之間不相容、自身團聚所造成的分散不均勻等問題。 其他燃料添加劑還包括金屬氧化物、過渡金屬氧化物 及雙環芳香族化合物,其中,金屬氧化物(如氧化辞、氧化 鎮)作為非勻相催化劑’雙環芳香族化合物作為還原劑。藉 由雙環芳香族化合物還原過渡金屬氧化物來活化金屬氧化 物進而提昇燃料的燃燒效率。但此添加劑中所使用的金 屬氧化物,除成本較高外,亦為毒性物質,長期使用會對 人體及環*兄造成負擔。另一種添加劑為可完全溶解於燃料 中的有機化合物(如笨曱酸),此種添加劑使燃料的密度及黏 度降低,幫助混合燃料中各種難溶組份,使燃料燃燒更完 由上述可知’目前的燃料添加劑除製程較複雜外,仍 有對%境及使用者造成危害之疑慮,因此,尋求僅需少量 添加且無毒無污染的燃料添加劑,實為迫切所需的❶ 【發明内容】 為了改善習知燃料添加劑之組份及製程繁雜、損害環 境及人體健康等問冑’本案發明人首先思及將昇華的概念 應用在燃料添加劑上,在多方試驗後,尋得—種無毒、= 乳味且僅需少量添加便可提昇液態燃料之燃燒效率的添加 劑。 因此,本發明之目的,即在提供一種用於提昇液態燃 201219555 料燃燒效率的添加劑,包人· 態燃料,其中,# 3 胃可昇華有機 下為固態。 一可昇華有機化合物及一液 化合物在一大氣壓及45°C以 本發明之另一 ^一目的在於提供一種用於提昇液態燃料燃 k政率的方法,县 _ ,, 疋透過將—可昇華有機化合物加入一液態 燃料中而完成,复中 ‘ /、中該可汁華有機化合物在一大氣壓及 45C以下為固態。, Lili's method. The existing methods for improving combustion efficiency are quite diverse, and in addition to the mechanical structure of the device, the use of various fuel additives is also known to the public. For example, adding 4~1〇 wt% methyl tert-butyl ether (MET) to unleaded gasoline can help complete combustion of gasoline and reduce carbon oxide emissions. However, methyl tert-butyl ether causes central nervous system damage, which may cause organ damage and cancer in long-term inhalation or exposure to methyl tert-butyl ether. The Republic of China Patent Publication No. 200927912 discloses an environmentally-friendly and fuel-efficient oil for vehicles and rolling boats. The liquid fuel-saving concentrate containing the energy activator and 2-methyl-2-propanol is uniformly mixed with the fuel in the fuel tank, which can improve the incomplete combustion of the fuel. The toxicity and anesthetic properties of 2-methyl-2-propanol used in this patent are higher than those of common alcohols. Therefore, the environmentally-friendly and oil-efficient oils still have doubts about the human body and the environment. The Republic of China Patent Publication No. 200825163 provides an energy-saving powder utilizing the principle of sub-shocking, which has far-infrared and negative ion efficiencies, is treated by nanotechnology and is oxidized by zinc oxide, cerium oxide, carbonic acid 201219555 It consists of magnesium, potassium oxide, aluminum oxide, rare earth elements and trace elements. This kind of fuel-saving powder is composed of a variety of solid inorganic materials and must be treated by nanotechnology. In addition to the complicated process, it is more likely to cause problems such as incompatibility with fuel and uneven dispersion caused by self-aggregation. Other fuel additives also include metal oxides, transition metal oxides, and bicyclic aromatic compounds in which metal oxides (e.g., oxidized, oxidized) are used as the non-homogeneous catalyst 'bicyclic aromatic compounds as reducing agents. The transition metal oxide is reduced by a bicyclic aromatic compound to activate the metal oxide to improve the combustion efficiency of the fuel. However, the metal oxide used in this additive is also a toxic substance in addition to the higher cost, and the long-term use imposes a burden on the human body and the ring. Another additive is an organic compound (such as scorpion acid) that is completely soluble in the fuel. This additive reduces the density and viscosity of the fuel, helps the various insoluble components in the fuel mixture, and makes the fuel burn more. In addition to the complicated process, the current fuel additives still have doubts about the harm to the environment and users. Therefore, it is urgent to find a fuel additive that requires only a small amount of addition and is non-toxic and non-polluting. [Inventive content] Improvement of the composition and process of conventional fuel additives, damage to the environment and human health. The inventor of this case first thought of applying the concept of sublimation to fuel additives. After multiple tests, it was found to be non-toxic, = milk. An additive that enhances the combustion efficiency of liquid fuels with a small addition. Accordingly, it is an object of the present invention to provide an additive for enhancing the combustion efficiency of a liquid fuel 201219555, which comprises a human fuel, wherein #3 can be sublimed organically in a solid state. A sublimable organic compound and a liquid compound at atmospheric pressure and 45 ° C. Another object of the present invention is to provide a method for increasing the fuel economy of a liquid fuel, and the county can be sublimated. The organic compound is added to a liquid fuel, and the organic compound in the middle of the complex is at a pressure of at most atmospheric pressure and below 45C.
中==明藉由添加一可昇華有機化合物至一液態燃料 :衣蜓/孤度上升時,該可昇華有機化合物將由固態昇 華:氣態’再由液態燃料釋出時,將於液態燃料中形成一 擾流:加強擴散型布朗運動,使得該液態燃料會因擾流而 句勻又熱且更易於轉化為小分子或氣態分子;&,透過該 可昇華有機化合物昇華轉變為氣態化合物,更可協助轉變 為小分子或氣態分子的液態燃料擴散並均勻地燃燒進而 提昇液態燃料的燃燒效率。本發明添加劑所含的可昇華有 機化合物具備無毒、低氣味且添加量少等優點,完全不會 造成環境及人體的傷害。 【實施方式】 本發明之一種用於提昇液態燃料燃燒效率的添加劑, 包含一可昇華有機化合物及一液態燃料,其中,該可昇華 有機化合物在一大氣壓及45°C以下為固態。 較佳地’該可昇華有機化合物含有一骨架,該骨架a 選自於雙環庚烷(bicyclic heptane)、萘(naphthalene)、二 τ ·*Λ* 茚(indan)、。比喃酮(pyrone)、環丙烷、環丁烷、環戊燒、淨 5 201219555 己烷、環庚烷、環辛烷或苯。 以下將依據上述所列舉之骨架,說明可昇華有機化合 物的例子: 1. 含有雙環庚烷骨架的可昇華有機化合物可包含,但不 限於:天然材料:如樟腦、茨醇(bornyl alcohol)、茨稀 (camphene)等。合成材料:例如:Medium == Ming by adding a sublimable organic compound to a liquid fuel: when the clothing/orphanity rises, the sublimable organic compound will be sublimated by the solid state: when the gaseous state is released from the liquid fuel, it will form in the liquid fuel. A turbulent flow: enhanced diffusion Brownian motion, which makes the liquid fuel uniform and hot due to turbulence and more easily converted into small molecules or gaseous molecules; &, through the sublimation of organic compounds, sublimation into gaseous compounds, The liquid fuel that can be converted into small molecules or gaseous molecules can be diffused and uniformly burned to improve the combustion efficiency of the liquid fuel. The sublimable organic compound contained in the additive of the present invention has the advantages of being non-toxic, low in odor, and having a small amount of addition, and does not cause environmental or human damage at all. [Embodiment] An additive for improving the combustion efficiency of a liquid fuel of the present invention comprises a sublimable organic compound and a liquid fuel, wherein the sublimable organic compound is solid at atmospheric pressure and below 45 °C. Preferably, the sublimable organic compound contains a skeleton selected from bicyclic heptane, naphthalene, and in?. Pyrone, cyclopropane, cyclobutane, cyclopentane, net 5 201219555 hexane, cycloheptane, cyclooctane or benzene. Examples of sublimable organic compounds will be described below based on the skeletons listed above: 1. Sublimable organic compounds containing a bicycloheptane skeleton may include, but are not limited to, natural materials such as camphor, bornyl alcohol, and Lean (camphene) and so on. Synthetic materials: for example:
[2-羥基-2,6,6-三曱基雙環[3.1.1]-2-庚烷] 其合成方法如下: ch3v^ch3[2-Hydroxy-2,6,6-trimethylbicyclo[3.1.1]-2-heptane] The synthesis method is as follows: ch3v^ch3
CH3 2HBr reflux _ H3C (THF) ch3v.ch3CH3 2HBr reflux _ H3C (THF) ch3v.ch3
3 NaOH3 NaOH
如下: [4,7,7-三甲基雙環[2.2.1]庚酮],其合成方法 201219555As follows: [4,7,7-trimethylbicyclo[2.2.1]heptanone], its synthesis method 201219555
Cl + 2 NaOH —► 〇H ΟCl + 2 NaOH —► 〇H Ο
Cl + 2 HC1Cl + 2 HC1
H3C^/CH3H3C^/CH3
,^^0H, ^^0H
[4,7,7-三甲基雙環[2.2.1]庚醇],其合成方法 如下:[4,7,7-trimethylbicyclo[2.2.1]heptanol], the synthesis method is as follows:
2. 含有萘骨架的可昇華有機化合物可包含但不限於:天 然材料如萘、β-萘甲醚(β-naphthol methylether)、β-萘 乙醚(β-naphtholethylether)等。 201219555 3. 含有二氫茚骨架的可昇華有機化合物可包含但不限 於:天然材料如5-乙醯基-1,1,2,3,3,6-六甲基二氫茚(5-acetyl-l,l,2,3,3,6-hexamethyl indan,phantolide)、4-乙 酿基-6-第三丁基-1,1_ 二甲基二氫茚(4-306{)^1-6461>1:-butyl-l,l-dimethylindan,celestolide)、1,1,4,4-四曱基-6-乙基-7-乙酿基-1,2,.3,4-四氫萘(1,1,4,4七的11^1171-6-ethyl-7-acetyl-l,2,3,4-tetrahydronaphthalene 5 versalide) 等。 4.含有°比喃酮骨架的可昇華有機化合物可包含但不限 於·天然材料如麥芽酚(malt〇l , 3-羥基_2_甲基_γ_吡喃 酮)。 5·含有環丙烷骨架的可昇華有機化合物可包含但不限 於:合成材料如: CH,2. The sublimable organic compound containing a naphthalene skeleton may include, but is not limited to, natural materials such as naphthalene, β-naphthol methylether, β-naphtholethylether, and the like. 201219555 3. Sublimable organic compounds containing an indoline skeleton may include, but are not limited to, natural materials such as 5-ethenyl-1,1,2,3,3,6-hexamethylindoline (5-acetyl) -l,l,2,3,3,6-hexamethyl indan,phantolide), 4-ethyl-branched-6-t-butyl-1,1-dimethyl indoline (4-306{)^1- 6461>1:-butyl-l,l-dimethylindan,celestolide), 1,1,4,4-tetradecyl-6-ethyl-7-ethenyl-1,2,.3,4-tetrahydrogen Naphthalene (11^1171-6-ethyl-7-acetyl-l, 2,3,4-tetrahydronaphthalene 5 versalide) of 1,1,4,4,7, and the like. 4. The sublimable organic compound containing a pyrone skeleton may include, but is not limited to, a natural material such as malt phenol (malt〇l, 3-hydroxy-2-methyl_γ-pyranone). 5. The sublimable organic compound containing a cyclopropane skeleton may include, but is not limited to, a synthetic material such as: CH,
[2-異丁基-3-異丙基環丙醇]、[2-isobutyl-3-isopropylcyclopropanol],
[2-異丁基·3_異丙基環丙酮]等。 3有環丁烷骨架的可昇華有機化合物 於·合成材料如: 可包含但不限 201219555[2-Isobutyl-3_isopropylcyclopropanone] and the like. 3 Sublimable organic compounds with a cyclobutane skeleton. Synthetic materials such as: May be included but not limited 201219555
ch3 [2-異丁基-4-乙基環丁醇]Ch3 [2-isobutyl-4-ethylcyclobutanol]
CH3 [2-異丁基-4-乙基環丁酮]等 7. 含有環戊烷骨架的可昇華有機化合物可包含但不限 於:合成材料如:CH3 [2-isobutyl-4-ethylcyclobutanone], etc. 7. The sublimable organic compound containing a cyclopentane skeleton may include, but is not limited to, a synthetic material such as:
ch3 h3c--ch3 [2-異丁基-4-曱基環戊醇]Ch3 h3c--ch3 [2-isobutyl-4-mercaptocyclopentanol]
h3c [2-異丁基-4-曱基環戊酮]等。 8. 含有環己烷骨架的可昇華有機化合物可包含但不限 於:天然材料如薄荷醇(menthol)、第三丁基環己醇 (tert-butylcyclohexanol)等。合成材料例如: 201219555H3c [2-isobutyl-4-mercaptocyclopentanone] and the like. 8. The sublimable organic compound containing a cyclohexane skeleton may include, but is not limited to, natural materials such as menthol, tert-butylcyclohexanol, and the like. Synthetic materials such as: 201219555
荷酮(menthol)],其合成方法如下:The ketone (menthol)], the synthesis method is as follows:
+ NaOH+ NaOH
衍 生自苧烯(limonene)],其合成方法如下: H3C、/Br ch3Derived from limonene], the synthesis method is as follows: H3C, /Br ch3
+ Br2 Δ reflux (THF) h3c-+ Br2 Δ reflux (THF) h3c-
Br CH,Br CH,
+ NaOH+ NaOH
H3C ^ch2H3C ^ch2
酮,衍生自香芹酮(carvone)],其合成方法如下: 10 201219555Ketone, derived from carvone, is synthesized as follows: 10 201219555
_(piperitone)],其合成方法如下:_ (piperitone)], its synthesis method is as follows:
H3C\/〇HH3C\/〇H
+ NaOH+ NaOH
h3c CH3 [5-羥基-5·曱基_2-(l-曱基亞乙基)環己烷,衍生自 胡薄荷顚I (pulegone)],其合成方法如下:H3c CH3 [5-Hydroxy-5.indolyl-2-(l-decylethylene)cyclohexane, derived from pulegone], is synthesized as follows:
++
+ NaOH+ NaOH
HSC CH3 [2_(4_羥基_4_曱基環己烷基)異丙醇,衍生自α_ 11 201219555 萜品醇(terpineol)],其合成方法如下 CH, H3C\/BrHSC CH3 [2_(4_hydroxy_4_decylcyclohexane)isopropanol, derived from α_ 11 201219555 terpineol], synthesized as follows CH, H3C\/Br
H3C. .OH Δ HBrH3C. .OH Δ HBr
OH reflux (THF) 火、 h3c/vch3OH reflux (THF) fire, h3c/vch3
+ NaOH+ NaOH
.OH j^OH h3c/^ch3.OH j^OH h3c/^ch3
H3C. .OH H3C 013 [1-羥基-1-曱基-4-(1-曱基亞乙基)環己烷,衍生自 萜品油烯(terpinolene)],其合成方法如下:H3C. .OH H3C 013 [1-hydroxy-1-indolyl-4-(1-mercaptoethylidene)cyclohexane, derived from terpinolene], is synthesized as follows:
+ NaOH+ NaOH
[1-羥基-2-異丁基環己烷],其合成方法如下:[1-Hydroxy-2-isobutylcyclohexane], which is synthesized as follows:
Cl Cl OHCl Cl OH
Cl2 ——► + HC1 + NaOHCl2 ——► + HC1 + NaOH
OH H2S04 CH3 ci士 CH3 CH, CH, "CH3 + Bf2 CH,OH H2S04 CH3 ci 士 CH3 CH, CH, "CH3 + Bf2 CH,
BrBr
OH CH, CH, -CH:OH CH, CH, -CH:
+ NaOH -CH3 CH, CH, 12 201219555+ NaOH -CH3 CH, CH, 12 201219555
[1-羥基-1-異丁基環己烷] 其合成方法如下:[1-Hydroxy-1-isobutylcyclohexane] The synthesis method is as follows:
OH CH, >~/ CH, H3C· -CH, CH3 /~ CH3 H0 [1,4-二羥基-3,6-二異丁基環己烷],其 合成方法如下: 2C1, -^ C1 〇OH CH, >~/ CH, H3C·-CH, CH3 /~ CH3 H0 [1,4-dihydroxy-3,6-diisobutylcyclohexane], the synthesis method is as follows: 2C1, -^ C1 〇
Cl + 2 HC1Cl + 2 HC1
Cl +2NaOH-►OH o + 2 严 A1C13 d〇i3 ^ H3C_ ch3 CH, ,__Λ CH, -CH, + Br,Cl +2NaOH-►OH o + 2 严 A1C13 d〇i3 ^ H3C_ ch3 CH, ,__Λ CH, -CH, + Br,
BrBr
OH CH, ,一_l CH, -CH, CH, _CH3 + 2NaOH—► H3C- ch3OH CH, , a _l CH, -CH, CH, _CH3 + 2NaOH—► H3C- ch3
HOHO
[1-羥基-3,6-二異丁基環己烷],其合成方法如 13 201219555 下:[1-Hydroxy-3,6-diisobutylcyclohexane], the synthesis method is as follows: 13 201219555
CH3 ——CH3 ch3CH3 ——CH3 ch3
HOHO
其合成方法如 [1-羥基-4-異丁基環己烷]Its synthesis method is [1-hydroxy-4-isobutylcyclohexane]
ch3 ——ch3 ch3Ch3 ——ch3 ch3
[2-異丁基環己酮],其合成方法如下: 14 201219555[2-Isobutylcyclohexanone], the synthesis method is as follows: 14 201219555
OHOH
CH3 [1-羥基-3-異丙基-6-曱基環己烷],其合成 方法如下:CH3 [1-hydroxy-3-isopropyl-6-fluorenylcyclohexane], which is synthesized as follows:
ch3 h3c--ch3Ch3 h3c--ch3
OHOH
[2-異丁基環己醇]、 15 201219555[2-isobutylcyclohexanol], 15 201219555
H3CH3C
[2_異丁基環己酮]等。 9.含有環庚院骨架的可昇基古換&人d J J什華有機化合物可包含但不 於:合成材料如: CH3\ /(¾ 限[2_Isobutylcyclohexanone] and the like. 9. Can be used in the ring-gathering framework. The human d J J Shihua organic compound may contain but not: synthetic materials such as: CH3\ / (3⁄4 limit
OHOH
[4-異丙基環庚醇]、[4-isopropylcycloheptanol],
CH3\ CHCH3\ CH
〇 [4-異丙基環庚酮]等。 含有環辛院骨架的可昇華有機化合物可包含但 於:合成材料如: 不限〇 [4-isopropylcycloheptanone] and the like. The sublimable organic compound containing the ring of the Xinxinyuan skeleton may include: synthetic materials such as:
不限於:合 11.含有苯骨架的可昇華有機化合物可包含但 成材料如: 16 201219555 [1-甲基-2,5-二異丁基_4_異丙基苯]等。It is not limited to: 11. The sublimable organic compound containing a benzene skeleton may be contained as a material such as: 16 201219555 [1-methyl-2,5-diisobutyl-4-isopropylbenzene].
^ >更佳地,該可昇華有機化合物是選自於樟腦、萘、薄 荷醇、茨醇、茇烯、第三丁基環己醇、麥芽酚、5-乙醯基· 1’1’2,3,3,6-六曱基二氫茚、4_乙醯基_6第三丁基Μ·二甲基 一虱印、1,1,4,4-四甲基_6·乙基_7•乙醢基义^心四氫蔡、 β_萘甲醚、β-蔡乙醚、2·異丙基_2,5_二羥基_5_甲基環己酮、 1-曱基-1-經基-4-(1_甲基·基乙基)環己烧、2_甲基_3•經 基-5-羥基-5-(1-甲基乙烯基)_2•環己酮' 弘曱基_3•羥基_6_異 丙基-環己嗣、5_經基_5_甲基_2_(1_甲基亞乙基)環己烷、2_ 羥基^-三甲基雙環^丄叫-庚院…心經基冰甲基小 環己烧基)異丙醇、卜經基]_甲基冬(1_甲基亞乙基)環己 烷、1-甲基-2,5-二異丁基_4_異丙基苯、卜經基-2_異丁基環 己烷、1·羥基_1_異丁基環己烷、M_二羥基·3,6_二異丁基環 己烷、1-經基-3,6-二異丁基環己烷、卜經基_心異丁基環己 烷、4,7,7-三甲基雙環[2.2]]庚酮、4,7,7_三甲基雙環[221] 庚醇、1-經基-3-異丙基_6·甲基環己烷、2_異丁基_3_異丙基 琢丙酮、2-異丁基_3_異丙基環丙醇、2_異丁基乙基環丁 酮、2-異丁基_4_乙基環丁醇、2_異丁基_4·甲基環戍酮、^ 異丁基-4-甲基裱戊醇、2_異丁基環己酮、2_異丁基環己醇、 4-異丙基%庚酮、4-異丙基環庚醇、3,7_二曱基環辛酮' 3,7-二甲基環辛酮’或上述可昇華有機化合物的—組合。又 更佳地,該可昇華有機化合物是選自於薄荷醇、茨醇、茨 17 201219555 烯、第三丁基環己醇、麥芽酚、5_乙醯基·丨山^ 6_六甲 基二氫節、4-乙醯基-6-第三丁基」,丨_二甲基二氫茚、 1,1,4,4-四曱基-6-乙基-7-乙醯基·1,2,3,4_四氫萘、β-萘甲 醚、β-萘乙醚、2-異丙基_2,5-二羥基-5-曱基環己酮、1-甲 基-1-羥基-4-(1-曱基-1-羥基乙基)環己烷、2_曱基_3_羥基_5_ 羥基-5-(1-甲基乙烯基)-2-環己酮、3_曱基_3_羥基_6_異丙基_ 環己酮、5-羥基-5-曱基·2·(1-曱基亞乙基)環己烷、2-羥基- 2.6.6- 三甲基雙環[3_1.1]-2-庚烷、2-(4-羥基-4-曱基-1-環己 烷基)異丙醇、1-羥基-1-曱基·4·(!_曱基亞乙基)環己烷、卜 甲基-2,5-二異丁基-4-異丙基苯、丨_羥基_2_異丁基環己烷、 1-羥基-1-異丁基環己烷、1,4_二羥基_3,6_二異丁基環己烷、 1-羥基-3,6-二異丁基環己烷、丨_羥基_4_異丁基環己烷、 4.7.7- 三曱基雙環[2.2· 1]庚酮、4,7,7-三曱基雙環[2.2.1]庚 醇、1-羥基-3-異丙基-6-甲基環己烷、2_異丁基_3_異丙基環 丙酮、2-異丁基-3-異丙基環丙醇、2_異丁基·4_乙基環丁 酮、2-異丁基-4-乙基環丁醇、2-異丁基曱基環戊酮、2-異丁基-4-曱基環戊醇、2-異丁基環己酮、2-異丁基環己醇、 4-異丙基環庚酮、4-異丙基環庚醇、3,7_二曱基環辛酮、 3.7- 二甲基環辛酮,或上述可昇華有機化合物的一組合。 上述之可昇華有機化合物為天然的成分或其衍生物, 部分帶有淡淡香氣,不會對環境造成負擔。 較佳地,每10公升的液態燃料添加〇 5〜5〇()公克的可 昇華有機化合物。 較佳地’該液態燃料是選自於汽油、柴油、酒精、生 18 201219555 質汽油、生質柴油、生質酒精、 負⑯有機氫化燃料油或上述燃 料之一組合。其中有機氫化燃料 了寸,由可例如但不限於環己 烧、甲基環己烷及十氫化萘。 θ發明之用於提昇液態燃料燃燒效率的方法是透過將一 可幵華有機化合物加人-液態燃料中而完成,《中,該可 昇華有機化合物與該液態燃料之態樣及變化是如上所=, 在此不多加費述。 本發明將就以下實施例來作進一步說明,但應瞭㈣ 是’該實施例僅為例示說明之用,而不應被解釋為本發明 實施之限制。^> More preferably, the sublimable organic compound is selected from the group consisting of camphor, naphthalene, menthol, benzyl alcohol, decene, t-butylcyclohexanol, maltol, 5-ethylindenyl 1'1 '2,3,3,6-hexamethylenedihydroindole, 4_acetamido_6 tert-butyl fluorene dimethyl oxime, 1,1,4,4-tetramethyl _6· Ethyl_7•Ethyl hydrazine, tetrahydrogen, β-naphthyl ether, β-caethyl ether, 2·isopropyl-2,5-dihydroxy-5-methylcyclohexanone, 1-曱1-yl-1-yl-4-(1-methylethyl)cyclohexanyl, 2-methyl-3-3-trans--5-hydroxy-5-(1-methylvinyl)_2• ring Hexanone 'Hongkung _3•hydroxyl_6_isopropyl-cyclohexanium, 5_carbyl_5_methyl_2_(1_methylethylidene)cyclohexane, 2_hydroxy^-three Methyl double ring ^ 丄 - 庚 庚 庚 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 庚 庚 庚 庚 庚 庚 庚 庚 庚 庚,5-diisobutyl-4_isopropylbenzene, bismyl-2-isobutylcyclohexane, 1·hydroxy_1_isobutylcyclohexane, M_dihydroxy·3,6_diiso Butylcyclohexane, 1-carbyl-3,6-diisobutylcyclohexane, dipyridyl-p-isobutylcyclohexane, 4,7,7-trimethylbicyclo[2 .2]]heptanone, 4,7,7-trimethylbicyclo[221]heptanol, 1-perzyl-3-isopropyl-6-methylcyclohexane, 2-isobutyl_3_ Isopropyl acetonone, 2-isobutyl _3_isopropylcyclopropanol, 2-isobutylethylcyclobutanone, 2-isobutyl-4-ethylcyclobutanol, 2-isobutyl _4·methylcyclononanone, ^isobutyl-4-methylamyl alcohol, 2-isobutylcyclohexanone, 2-isobutylcyclohexanol, 4-isopropyl% heptanone, 4-isopropylcycloheptanol, 3,7-didecylcyclooctanone '3,7-dimethylcyclooctanone' or a combination of the above sublimable organic compounds. More preferably, the sublimable organic compound is selected from the group consisting of menthol, benzyl alcohol, Benz 17 201219555 olefin, tert-butylcyclohexanol, maltol, 5-ethylidene·丨山^ 6_hexa Dihydrogen, 4-ethinyl-6-t-butyl", 丨-dimethyl indoline, 1,1,4,4-tetradecyl-6-ethyl-7-ethenyl · 1,2,3,4_tetrahydronaphthalene, β-naphthylmethyl ether, β-naphthyl ether, 2-isopropyl-2,5-dihydroxy-5-fluorenylcyclohexanone, 1-methyl- 1-hydroxy-4-(1-mercapto-1-hydroxyethyl)cyclohexane, 2-hydrazino-3-hydroxy-5-hydroxy-5-(1-methylvinyl)-2-cyclohexanone 3_曱基_3_hydroxy_6_isopropyl_cyclohexanone, 5-hydroxy-5-fluorenyl-2(1-mercaptoethylidene)cyclohexane, 2-hydroxy-2.6. 6-trimethylbicyclo[3_1.1]-2-heptane, 2-(4-hydroxy-4-mercapto-1-cyclohexane)isopropanol, 1-hydroxy-1-indenyl·4 · (!_曱-ethylidene) cyclohexane, methyl-2,5-diisobutyl-4-isopropylbenzene, hydrazine-hydroxy-2-isobutylcyclohexane, 1-hydroxy-1 -isobutylcyclohexane, 1,4-dihydroxy-3,6-diisobutylcyclohexane, 1-hydroxy-3,6-diisobutylcyclohexane, 丨_hydroxy_4_ Butylcyclohexane, 4.7.7-three Bicyclo[2.2.1]heptanone, 4,7,7-trimercaptobicyclo[2.2.1]heptanol, 1-hydroxy-3-isopropyl-6-methylcyclohexane, 2-isobutyl Base_3_isopropylcyclopropanone, 2-isobutyl-3-isopropylcyclopropanol, 2-isobutyl-4-isocyclobutanone, 2-isobutyl-4-ethylcyclo Butanol, 2-isobutyldecylcyclopentanone, 2-isobutyl-4-mercaptocyclopentanol, 2-isobutylcyclohexanone, 2-isobutylcyclohexanol, 4-isopropyl A cyclohexanone, 4-isopropylcycloheptanol, 3,7-didecylcyclooctanone, 3.7-dimethylcyclooctanone, or a combination of the above sublimable organic compounds. The above-mentioned sublimable organic compound is a natural component or a derivative thereof, and partially has a light aroma, and does not burden the environment. Preferably, 5 to 5 Å (grams) of sublimable organic compound is added per 10 liters of liquid fuel. Preferably, the liquid fuel is selected from the group consisting of gasoline, diesel, alcohol, raw gasoline, biodiesel, raw alcohol, negative 16 organic hydrogenated fuel oil, or a combination of the foregoing. Among them, the organic hydrogenated fuel may be, for example, but not limited to, cyclohexene, methylcyclohexane and decalin. The method for increasing the combustion efficiency of a liquid fuel by θ is accomplished by adding a Kelly organic compound to a human-liquid fuel, wherein the sublimation organic compound and the liquid fuel are as described above. =, there is no more to mention here. The invention is further illustrated by the following examples, which are intended to be illustrative only and not to be construed as limiting.
<實施例> [實施例1J 將2.5公克的1_經基_4_異丁基環己烧加入5〇公升的 市售柴油中,製得實施例1之添加劑。 (測試)將實施例1的添加劑加入一柴油車TUCS〇ND_ DX2(排氣量為2000C.C.,馬力為136hp,2〇〇7年 11月出廠)的空油箱中,於一般道路上不定速行 駛,測試該柴油車可行駛之公里數,獲得之公里 數為560公里。(測試地點為大陸深圳) (二白试驗)使用上述測試的同一柴油車,並於其空油箱 中加入50公升的柴油’再測試該柴油車於 一般道路上不定速可行駛之公里數,獲得之 公里數為480公里。 (結果)由上述結果可知,實施例1的添加劑可讓柴油車 19 201219555 【實ι 可行駛之公里數由480公里提昇至560公里。 I頁苑例2】 字2.5公克的2 -異丁基環己酮加入6〇公升的95無錯 ^气ί由 '干’製得實施例2之添加劑。 (測執) ^ 將貫施例2的添加劑加入一汽油車奥迪A8〇(排氣 量為2000C.C. ’馬力為175hp,2002年10月出 廠)的空油箱中’於一般道路上不定速行駛,測試 該汽油車可行駛之公里數’獲得之公里數為43〇 公里。(測試地點為大陸深圳) 試驗)使用上述測試的同一汽油車,並於其空油箱 中加入60公升的95無鉛汽油,再測試該汽 油車於一般道路上不定速可行駛之公里數, 獲得之公里數為350公里。 (結果)由上述結果可知,實施例2的添加劑可讓汽油車 可行駛之公里數由350公里提昇至43〇公里。 [實施例3】 將2.5公克# i,基_3_異丙基_6•甲基環己烷加入% 公升的97無鉛汽油中,製得實施例3之添加劑。 (測試)f實施例3的添加劑加入一汽油車本田雅哥(排氣 量為3000C.C.,馬力為2〇〇hp,2〇〇3年6月出廠) 的空油箱中,於—般道路上不定速行駛’測試該 汽油車可行驶之公里數,獲得之公里數為450公 里。(測試地點為大陸深圳) (空白試驗)使用上述測試的同一汽油車,並於其空油箱 20 201219555 :=5°公升的97無敍汽油’再測試該汽 油車於一般道路上不定速可行歇之公里數, 獲得之公里數為350公里。 (結果)自上述結果可知,實施例3的添加劑可讓汽油車 可行駛之公里數由350公里提昇至45〇公 [實施例4] (測試) —將2.5公克的2•異丁基環己醇加入6〇公升的%無錯 汽油中,製得實施例4之添加劑。 ‘·'、。<Examples> [Example 1J An additive of Example 1 was obtained by adding 2.5 g of 1-_base-based 4-isobutylcyclohexane to 5 liters of commercially available diesel oil. (Test) Add the additive of Example 1 to an empty fuel tank of a diesel vehicle TUCS 〇 ND_ DX2 (with a displacement of 2000 C.C., a horsepower of 136 hp, which was delivered in November 2007). At a fixed speed, test the number of kilometers that the diesel car can travel, and the number of kilometers obtained is 560 kilometers. (The test location is Shenzhen, China) (Two white test) The same diesel vehicle tested above was used, and 50 liters of diesel oil was added to its empty fuel tank. Then test the number of kilometers that the diesel vehicle can travel at a fixed speed on a general road. The number of kilometers obtained is 480 kilometers. (Results) From the above results, it is understood that the additive of the embodiment 1 can make the diesel vehicle 19 201219555 [the number of kilometers that can be traveled from 480 km to 560 km. I Page 2 Example 2] 2.5 g of 2-isobutylcyclohexanone was added to 6 liters of 95 without error. The additive of Example 2 was obtained from 'dry'. (Measurement and Control) ^ Add the additive of Example 2 to a petrol car Audi A8 〇 (displacement of 2000C.C. 'horsepower is 175hp, factory in October 2002) in the empty fuel tank 'on the general road uncertain Speed driving, test the number of kilometers that the gasoline car can travel 'the number of kilometers obtained is 43 kilometers. (Test location is Shenzhen, China) Test) Use the same gasoline vehicle tested above, and add 60 liters of 95 unleaded gasoline to its empty fuel tank, and then test the number of kilometers that the gasoline vehicle can travel at a fixed speed on a general road. The number of kilometers is 350 kilometers. (Results) From the above results, the additive of Example 2 can increase the number of kilometers that a gasoline vehicle can travel from 350 kilometers to 43 kilometers. [Example 3] An additive of Example 3 was obtained by adding 2.5 gram of # i, ki_3_isopropyl_6-methylcyclohexane to a % liter of 97 unleaded gasoline. (Test) f The additive of Example 3 was added to an empty fuel tank of a gasoline vehicle Honda Yage (with a displacement of 3000 C.C., a horsepower of 2 hp, and a delivery of 2 〇〇 3 years). Driving at a fixed speed on the road' test the number of kilometers that the petrol car can travel, and the number of kilometers obtained is 450 kilometers. (Test location is Shenzhen, China) (Blank test) Use the same gasoline vehicle tested above, and in its empty fuel tank 20 201219555: = 5 ° liter of 97 unsold gasoline 'retest the gasoline vehicle on the general road at a fixed speed The number of kilometers to rest, the number of kilometers obtained is 350 kilometers. (Results) From the above results, the additive of Example 3 can increase the number of kilometers that can be driven by a gasoline vehicle from 350 km to 45 [ [Example 4] (test) - 2.5 g of 2 • isobutylcyclohexane The additive of Example 4 was prepared by adding alcohol to 6 liters of % error free gasoline. ‘·’,.
將實施例4的添加劑加入一汽油車奥迪A8〇(排氣 量為2000C.C.,馬力為1?5邱’ 2〇〇2年ι〇月出 廢)的空油箱中’於—般道路上不定速行歇測試 該汽油車可行駛之公里數,獲得之公里數為46〇 公里^ (測試地點為大陸深圳) (空白試驗)使用上述測試的同一汽油車,並於其空油箱 中加入60公升的95無鉛汽油, *車於-般道路上不定速可行故之公丨:: 獲得之公里數為350公里。 (結果) 由上述結果可知,實施例4的添加劑可讓汽油車 可行駛之公里數由350公里提昇至460公里。 [實施例5】 將2.5公克的2_異丁基環己酮加入50公升的97無鉛 汽油中,製得實施例5之添加劑。 …° (測試)冑實施例5的添加劑加入一汽油車本田雅哥(排氣 $為3000C.C.,馬力為2〇〇hp,2〇〇3年6月出廠) 21 201219555 的空油箱中,於一般道路上不定速行駛測試該 汽油車可行駛之公里數,獲得之公里數為440公 里。(測試地點為大陸深圳) (空白試驗)使用上述測試的同一汽油車,並於其空油箱 中加入50公升的97無鉛汽油,再測試該汽 油車於一般道路上不定速可行駛之公里數, 獲得之公里數為350公里。 (結果)自上述結果可知,實施例5的添加劑可讓汽油車 可行駛之公里數由350公里提昇至44〇公里。Adding the additive of Example 4 to the empty tank of a gasoline car Audi A8〇 (with a displacement of 2000C.C., a horsepower of 1?5 Qiu '2〇〇2 years ι〇月) The number of kilometers that the petrol car can travel is tested on the speed limit, and the number of kilometers obtained is 46〇 km ^ (test location is Shenzhen, China) (blank test) using the same gasoline car tested above, and in its empty fuel tank Add 60 liters of 95 unleaded petrol, *The car is not allowed to speed on the road - the number of kilometers is 350 kilometers. (Results) From the above results, the additive of Example 4 can increase the number of kilometers that a gasoline vehicle can travel from 350 km to 460 km. [Example 5] An additive of Example 5 was obtained by adding 2.5 g of 2-isobutylcyclohexanone to 50 liter of 97 unleaded gasoline. ...° (test) 添加剂 The additive of Example 5 was added to a gasoline vehicle Honda Yage (exhaust $ 3000C.C., horsepower 2 hp, 2 〇〇 3 years in June) 21 201219555 in the empty fuel tank The number of kilometers that the gasoline vehicle can travel is tested at a fixed speed on a general road, and the number of kilometers obtained is 440 kilometers. (Test location is Shenzhen, China) (Blank test) Use the same gasoline vehicle tested above, and add 50 liters of 97 unleaded gasoline to its empty fuel tank, and test the number of kilometers that the gasoline vehicle can travel at a fixed speed on a general road. The number of kilometers obtained is 350 kilometers. (Results) From the above results, the additive of Example 5 can increase the number of kilometers that a gasoline vehicle can travel from 350 kilometers to 44 kilometers.
[實施例6J 將2.5公克的4,7,7_三甲基雙環[22 ^庚醇加入%公 升的97無鉛汽油中’製得實施例6之添加劑。 (測試)冑實施例6的添加劑加人-汽油車本田雅哥(排氣 量為3000C.C.,馬力為2〇〇hp,2003年6月出廠) 的空油箱中,於一般道路上不定速行駛,測試該 汽油車可行駛之公里數,獲得之公里數為47〇公 里。(測試地點為大陸深圳) (空白試驗)使用上述測試的同一汽油車,並於其空油箱 中加入50公升的97無紹汽油,再測試該汽 油車於一般道路上不定速可行駛之公里數, 獲得之公里數為350公里。 (結果)&上述結果可知,實施例6的添加劑可讓汽油車 可行駛之公里數由350公里提昇至47〇公里。[Example 6J An additive of Example 6 was prepared by adding 2.5 g of 4,7,7-trimethylbicyclo [22 ^heptanol to % liter of 97 unleaded gasoline]. (Test) 胄 The additive of the example 6 is added to the empty fuel tank of the gasoline-powered Honda Yage (3000 C.C., horsepower 2 hp, factory delivered in June 2003), not on the general road. At a fixed speed, test the number of kilometers that the gasoline car can travel, and the number of kilometers obtained is 47 kilometers. (Test location is Shenzhen, China) (Blank test) Use the same gasoline vehicle tested above, and add 50 liters of 97 non-salted gasoline to its empty fuel tank, and then test the gasoline vehicle to travel at a fixed speed on the general road. The number of kilometers obtained is 350 kilometers. (Results) & The above results show that the additive of Example 6 can increase the number of kilometers that a gasoline vehicle can travel from 350 kilometers to 47 kilometers.
[實施例7J 22 201219555 將2,5公克的4,7,7-三甲基雙環[叫庚嗣加入50公 升的市售柴油中’製得實施例7之添加劑。 (測試)將實施例7的添加劑加入—柴油車TUCS嶋_ M2(排氣量為2〇〇〇C.C.,馬力為136hp,2007年 U月出廠)的空油箱中,於-般道路上不定速行 駛,測試該柴油車可行驶之公里數,獲得之公里 數為590公里。(測試地點為大陸深圳)[Example 7J 22 201219555 An additive of Example 7 was prepared by adding 2,5 g of 4,7,7-trimethylbicyclo [called gadolinium to 50 liters of commercially available diesel oil]. (Test) Adding the additive of Example 7 to the empty fuel tank of diesel vehicle TUCS嶋_ M2 (exhaust volume 2〇〇〇CC, horsepower 136hp, factory delivery in 2007), uncertain on the road Drive at speed and test the number of kilometers that the diesel car can travel. The number of kilometers obtained is 590 kilometers. (Test location is Shenzhen, China)
(空白試驗)冑用上述測試的同一柴油車,並於其空油箱 中加入50公升的柴油,再測試該柴油車於 一般道路上不定速可行駛之公里數,獲得之 公里數為480公里。 (結果)纟上述結果可知,實施例7的添加劑可讓柴油車 可打駛之公里數由480公里提昇至59〇公里。 亦上所述,本發明一種用於提昇液態燃料燃燒效率的 添加劑,藉由添加劑中的可昇華有機化合物,以昇華體積 膨脹的物理現象造成液態燃料授動,讓液態燃料可以均勾 受熱而轉化為小分子或氣態分子,進而使該液態燃料之燃 燒效岸明顯上升,以讓液態燃料充分運用,達到兼顧環保 與省油的目的。 ' .惟以上所述者,僅為本發明之較佳實施例而已,當不 月&以此限定本發B月實施之範圍,即大凡依本發明申請專利 範圍及發明說明内容所作之簡單的等效變化與修飾,皆仍 屬本發明專利涵蓋之範圍内。 23 201219555 【圖式簡單說明】 201219555 【主要元件符號說明】 無(Blank test) The same diesel vehicle tested above was used, and 50 liters of diesel oil was added to its empty fuel tank, and the number of kilometers that the diesel vehicle was able to travel at a fixed speed on a general road was tested. The number of kilometers obtained was 480 km. . (Results) As can be seen from the above results, the additive of Example 7 can increase the number of kilometers that a diesel vehicle can drive from 480 kilometers to 59 kilometers. In addition, the present invention relates to an additive for improving the combustion efficiency of a liquid fuel, which can be converted by a physical phenomenon of sublimation volume expansion by a sublimable organic compound in the additive, so that the liquid fuel can be transformed by heat. It is a small molecule or a gaseous molecule, which in turn makes the combustion effect of the liquid fuel rise significantly, so that the liquid fuel can be fully utilized to achieve environmental protection and fuel economy. The above is only the preferred embodiment of the present invention, and the scope of the implementation of the present invention is limited, and the simplicity of the invention is based on the scope of the invention and the description of the invention. Equivalent variations and modifications are still within the scope of the invention. 23 201219555 [Simplified illustration] 201219555 [Explanation of main component symbols]
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TW099138652A TW201219555A (en) | 2010-11-10 | 2010-11-10 | promoting the Brownian motion by the addition of a sublimatable organic compound |
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