WO2011075420A1 - Methods for analyzing and optimizing biofuel compositions - Google Patents
Methods for analyzing and optimizing biofuel compositions Download PDFInfo
- Publication number
- WO2011075420A1 WO2011075420A1 PCT/US2010/059985 US2010059985W WO2011075420A1 WO 2011075420 A1 WO2011075420 A1 WO 2011075420A1 US 2010059985 W US2010059985 W US 2010059985W WO 2011075420 A1 WO2011075420 A1 WO 2011075420A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- fatty acid
- acid alkyl
- nitrate
- spectrophotometer
- biodiesel
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 110
- 238000000034 method Methods 0.000 title claims abstract description 75
- 239000002551 biofuel Substances 0.000 title claims abstract description 48
- 239000003225 biodiesel Substances 0.000 claims abstract description 131
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 121
- 239000000194 fatty acid Substances 0.000 claims abstract description 121
- 229930195729 fatty acid Natural products 0.000 claims abstract description 121
- 125000005907 alkyl ester group Chemical group 0.000 claims description 63
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 claims description 56
- 150000004702 methyl esters Chemical class 0.000 claims description 50
- 239000000446 fuel Substances 0.000 claims description 45
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 claims description 26
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 claims description 25
- 235000021281 monounsaturated fatty acids Nutrition 0.000 claims description 23
- 235000020777 polyunsaturated fatty acids Nutrition 0.000 claims description 23
- 229920006395 saturated elastomer Polymers 0.000 claims description 23
- FLIACVVOZYBSBS-UHFFFAOYSA-N Methyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC FLIACVVOZYBSBS-UHFFFAOYSA-N 0.000 claims description 19
- 150000004665 fatty acids Chemical class 0.000 claims description 18
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 16
- 238000002835 absorbance Methods 0.000 claims description 16
- 238000004817 gas chromatography Methods 0.000 claims description 15
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 14
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 claims description 14
- 238000002156 mixing Methods 0.000 claims description 14
- 235000019482 Palm oil Nutrition 0.000 claims description 13
- 239000002540 palm oil Substances 0.000 claims description 13
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 claims description 12
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 12
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 12
- SECPZKHBENQXJG-FPLPWBNLSA-N palmitoleic acid Chemical compound CCCCCC\C=C/CCCCCCCC(O)=O SECPZKHBENQXJG-FPLPWBNLSA-N 0.000 claims description 12
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 11
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 11
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 11
- 239000005642 Oleic acid Substances 0.000 claims description 11
- 235000019484 Rapeseed oil Nutrition 0.000 claims description 11
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 11
- 239000003760 tallow Substances 0.000 claims description 11
- 239000003963 antioxidant agent Substances 0.000 claims description 10
- QYDYPVFESGNLHU-UHFFFAOYSA-N elaidic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCC(=O)OC QYDYPVFESGNLHU-UHFFFAOYSA-N 0.000 claims description 10
- 239000003549 soybean oil Substances 0.000 claims description 10
- 235000012424 soybean oil Nutrition 0.000 claims description 10
- LVGKNOAMLMIIKO-UHFFFAOYSA-N Elaidinsaeure-aethylester Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC LVGKNOAMLMIIKO-UHFFFAOYSA-N 0.000 claims description 9
- 239000000654 additive Substances 0.000 claims description 9
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 claims description 9
- 230000004044 response Effects 0.000 claims description 9
- 230000001276 controlling effect Effects 0.000 claims description 8
- 150000002148 esters Chemical class 0.000 claims description 8
- 235000020778 linoleic acid Nutrition 0.000 claims description 8
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 claims description 8
- 239000003209 petroleum derivative Substances 0.000 claims description 8
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims description 8
- 230000003078 antioxidant effect Effects 0.000 claims description 7
- 239000003921 oil Substances 0.000 claims description 7
- 235000019198 oils Nutrition 0.000 claims description 7
- 235000021314 Palmitic acid Nutrition 0.000 claims description 6
- 235000021319 Palmitoleic acid Nutrition 0.000 claims description 6
- 238000013528 artificial neural network Methods 0.000 claims description 6
- SECPZKHBENQXJG-UHFFFAOYSA-N cis-palmitoleic acid Natural products CCCCCCC=CCCCCCCCC(O)=O SECPZKHBENQXJG-UHFFFAOYSA-N 0.000 claims description 6
- 238000005260 corrosion Methods 0.000 claims description 6
- 230000007797 corrosion Effects 0.000 claims description 6
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 claims description 6
- NKRVGWFEFKCZAP-UHFFFAOYSA-N 2-ethylhexyl nitrate Chemical group CCCCC(CC)CO[N+]([O-])=O NKRVGWFEFKCZAP-UHFFFAOYSA-N 0.000 claims description 5
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 claims description 5
- 239000003240 coconut oil Substances 0.000 claims description 5
- 235000019864 coconut oil Nutrition 0.000 claims description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 4
- 241000221089 Jatropha Species 0.000 claims description 4
- 238000005481 NMR spectroscopy Methods 0.000 claims description 4
- 229910002651 NO3 Inorganic materials 0.000 claims description 4
- 230000000996 additive effect Effects 0.000 claims description 4
- 238000009835 boiling Methods 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims description 4
- 239000010949 copper Substances 0.000 claims description 4
- 235000005687 corn oil Nutrition 0.000 claims description 4
- 239000002285 corn oil Substances 0.000 claims description 4
- HLYOOCIMLHNMOG-UHFFFAOYSA-N cyclohexyl nitrate Chemical compound [O-][N+](=O)OC1CCCCC1 HLYOOCIMLHNMOG-UHFFFAOYSA-N 0.000 claims description 4
- 238000001030 gas--liquid chromatography Methods 0.000 claims description 4
- 230000005484 gravity Effects 0.000 claims description 4
- 150000002500 ions Chemical class 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 4
- 238000004876 x-ray fluorescence Methods 0.000 claims description 4
- BITHHVVYSMSWAG-KTKRTIGZSA-N (11Z)-icos-11-enoic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCC(O)=O BITHHVVYSMSWAG-KTKRTIGZSA-N 0.000 claims description 3
- WTTJVINHCBCLGX-UHFFFAOYSA-N (9trans,12cis)-methyl linoleate Natural products CCCCCC=CCC=CCCCCCCCC(=O)OC WTTJVINHCBCLGX-UHFFFAOYSA-N 0.000 claims description 3
- TWJNQYPJQDRXPH-UHFFFAOYSA-N 2-cyanobenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1C#N TWJNQYPJQDRXPH-UHFFFAOYSA-N 0.000 claims description 3
- HWMKUXXLKIOVQZ-UHFFFAOYSA-N 3,6-dimethylpyridin-2-amine Chemical compound CC1=CC=C(C)C(N)=N1 HWMKUXXLKIOVQZ-UHFFFAOYSA-N 0.000 claims description 3
- 235000021357 Behenic acid Nutrition 0.000 claims description 3
- 235000021360 Myristic acid Nutrition 0.000 claims description 3
- 235000021355 Stearic acid Nutrition 0.000 claims description 3
- 235000019486 Sunflower oil Nutrition 0.000 claims description 3
- 235000020661 alpha-linolenic acid Nutrition 0.000 claims description 3
- 229940116226 behenic acid Drugs 0.000 claims description 3
- 239000000828 canola oil Substances 0.000 claims description 3
- 235000019519 canola oil Nutrition 0.000 claims description 3
- 239000008162 cooking oil Substances 0.000 claims description 3
- 230000002596 correlated effect Effects 0.000 claims description 3
- KFEVDPWXEVUUMW-UHFFFAOYSA-N docosanoic acid Natural products CCCCCCCCCCCCCCCCCCCCCC(=O)OCCC1=CC=C(O)C=C1 KFEVDPWXEVUUMW-UHFFFAOYSA-N 0.000 claims description 3
- 229940108623 eicosenoic acid Drugs 0.000 claims description 3
- BITHHVVYSMSWAG-UHFFFAOYSA-N eicosenoic acid Natural products CCCCCCCCC=CCCCCCCCCCC(O)=O BITHHVVYSMSWAG-UHFFFAOYSA-N 0.000 claims description 3
- 239000003623 enhancer Substances 0.000 claims description 3
- 239000004519 grease Substances 0.000 claims description 3
- 229960004488 linolenic acid Drugs 0.000 claims description 3
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 claims description 3
- WTTJVINHCBCLGX-NQLNTKRDSA-N methyl linoleate Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(=O)OC WTTJVINHCBCLGX-NQLNTKRDSA-N 0.000 claims description 3
- POULHZVOKOAJMA-UHFFFAOYSA-N methyl undecanoic acid Natural products CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 claims description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims description 3
- 239000004006 olive oil Substances 0.000 claims description 3
- 235000008390 olive oil Nutrition 0.000 claims description 3
- 239000008117 stearic acid Substances 0.000 claims description 3
- 239000002600 sunflower oil Substances 0.000 claims description 3
- PSTVZBXGCKLSQA-UHFFFAOYSA-N (1-methylcyclohexyl) nitrate Chemical compound [O-][N+](=O)OC1(C)CCCCC1 PSTVZBXGCKLSQA-UHFFFAOYSA-N 0.000 claims description 2
- OLJOBIJKBAHJBG-UHFFFAOYSA-N (1-propan-2-ylcyclohexyl) nitrate Chemical compound [O-][N+](=O)OC1(C(C)C)CCCCC1 OLJOBIJKBAHJBG-UHFFFAOYSA-N 0.000 claims description 2
- ATNNLHXCRAAGJS-QZQOTICOSA-N (e)-docos-2-enoic acid Chemical compound CCCCCCCCCCCCCCCCCCC\C=C\C(O)=O ATNNLHXCRAAGJS-QZQOTICOSA-N 0.000 claims description 2
- YLHLAFNDCKPBPP-UHFFFAOYSA-N 1-ethoxybutyl nitrate Chemical compound CCCC(OCC)O[N+]([O-])=O YLHLAFNDCKPBPP-UHFFFAOYSA-N 0.000 claims description 2
- DBZSUXCRERIXBX-UHFFFAOYSA-N 1-propan-2-yloxybutyl nitrate Chemical compound CCCC(OC(C)C)O[N+]([O-])=O DBZSUXCRERIXBX-UHFFFAOYSA-N 0.000 claims description 2
- UENFRVTUGZKXNH-UHFFFAOYSA-N 2-methylbutan-2-yl nitrate Chemical compound CCC(C)(C)O[N+]([O-])=O UENFRVTUGZKXNH-UHFFFAOYSA-N 0.000 claims description 2
- LNNXFUZKZLXPOF-UHFFFAOYSA-N 2-methylpropyl nitrate Chemical compound CC(C)CO[N+]([O-])=O LNNXFUZKZLXPOF-UHFFFAOYSA-N 0.000 claims description 2
- NTHGIYFSMNNHSC-UHFFFAOYSA-N 3-methylbutyl nitrate Chemical compound CC(C)CCO[N+]([O-])=O NTHGIYFSMNNHSC-UHFFFAOYSA-N 0.000 claims description 2
- 235000019737 Animal fat Nutrition 0.000 claims description 2
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 claims description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 2
- HSNWZBCBUUSSQD-UHFFFAOYSA-N amyl nitrate Chemical compound CCCCCO[N+]([O-])=O HSNWZBCBUUSSQD-UHFFFAOYSA-N 0.000 claims description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000003139 biocide Substances 0.000 claims description 2
- DYONNFFVDNILGI-UHFFFAOYSA-N butan-2-yl nitrate Chemical compound CCC(C)O[N+]([O-])=O DYONNFFVDNILGI-UHFFFAOYSA-N 0.000 claims description 2
- QQHZPQUHCAKSOL-UHFFFAOYSA-N butyl nitrate Chemical compound CCCCO[N+]([O-])=O QQHZPQUHCAKSOL-UHFFFAOYSA-N 0.000 claims description 2
- 239000012459 cleaning agent Substances 0.000 claims description 2
- DDBCVXXAMXPHKF-UHFFFAOYSA-N cyclopentyl nitrate Chemical compound [O-][N+](=O)OC1CCCC1 DDBCVXXAMXPHKF-UHFFFAOYSA-N 0.000 claims description 2
- UEFBRXQBUTYIJI-UHFFFAOYSA-N decyl nitrate Chemical compound CCCCCCCCCCO[N+]([O-])=O UEFBRXQBUTYIJI-UHFFFAOYSA-N 0.000 claims description 2
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 claims description 2
- PAWHIGFHUHHWLN-UHFFFAOYSA-N dodecyl nitrate Chemical compound CCCCCCCCCCCCO[N+]([O-])=O PAWHIGFHUHHWLN-UHFFFAOYSA-N 0.000 claims description 2
- IDNUEBSJWINEMI-UHFFFAOYSA-N ethyl nitrate Chemical compound CCO[N+]([O-])=O IDNUEBSJWINEMI-UHFFFAOYSA-N 0.000 claims description 2
- HHXLSUKHLTZWKR-UHFFFAOYSA-N heptan-2-yl nitrate Chemical compound CCCCCC(C)O[N+]([O-])=O HHXLSUKHLTZWKR-UHFFFAOYSA-N 0.000 claims description 2
- JYMDZTRYDIQILZ-UHFFFAOYSA-N heptyl nitrate Chemical compound CCCCCCCO[N+]([O-])=O JYMDZTRYDIQILZ-UHFFFAOYSA-N 0.000 claims description 2
- AGDYNDJUZRMYRG-UHFFFAOYSA-N hexyl nitrate Chemical compound CCCCCCO[N+]([O-])=O AGDYNDJUZRMYRG-UHFFFAOYSA-N 0.000 claims description 2
- 239000003112 inhibitor Substances 0.000 claims description 2
- GAPFWGOSHOCNBM-UHFFFAOYSA-N isopropyl nitrate Chemical compound CC(C)O[N+]([O-])=O GAPFWGOSHOCNBM-UHFFFAOYSA-N 0.000 claims description 2
- 239000006078 metal deactivator Substances 0.000 claims description 2
- LRMHVVPPGGOAJQ-UHFFFAOYSA-N methyl nitrate Chemical compound CO[N+]([O-])=O LRMHVVPPGGOAJQ-UHFFFAOYSA-N 0.000 claims description 2
- CMNNRVWVNGXINV-UHFFFAOYSA-N nonyl nitrate Chemical compound CCCCCCCCCO[N+]([O-])=O CMNNRVWVNGXINV-UHFFFAOYSA-N 0.000 claims description 2
- QCOKASLKYUXYJH-UHFFFAOYSA-N octan-2-yl nitrate Chemical compound CCCCCCC(C)O[N+]([O-])=O QCOKASLKYUXYJH-UHFFFAOYSA-N 0.000 claims description 2
- TXQBMQNFXYOIPT-UHFFFAOYSA-N octyl nitrate Chemical compound CCCCCCCCO[N+]([O-])=O TXQBMQNFXYOIPT-UHFFFAOYSA-N 0.000 claims description 2
- OTRMXXQNSIVZNR-UHFFFAOYSA-N prop-2-enyl nitrate Chemical compound [O-][N+](=O)OCC=C OTRMXXQNSIVZNR-UHFFFAOYSA-N 0.000 claims description 2
- AZAKMLHUDVIDFN-UHFFFAOYSA-N tert-butyl nitrate Chemical compound CC(C)(C)O[N+]([O-])=O AZAKMLHUDVIDFN-UHFFFAOYSA-N 0.000 claims description 2
- 239000005749 Copper compound Substances 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 150000001880 copper compounds Chemical class 0.000 claims 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 claims 1
- 238000001871 ion mobility spectroscopy Methods 0.000 claims 1
- 239000002530 phenolic antioxidant Substances 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- WMYJOZQKDZZHAC-UHFFFAOYSA-H trizinc;dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S WMYJOZQKDZZHAC-UHFFFAOYSA-H 0.000 claims 1
- 238000013461 design Methods 0.000 abstract description 5
- 235000019387 fatty acid methyl ester Nutrition 0.000 description 13
- 239000002283 diesel fuel Substances 0.000 description 9
- 239000008158 vegetable oil Substances 0.000 description 7
- 238000004458 analytical method Methods 0.000 description 6
- -1 fatty acid esters Chemical class 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 238000002330 electrospray ionisation mass spectrometry Methods 0.000 description 5
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 5
- 229940057007 petroleum distillate Drugs 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 235000013311 vegetables Nutrition 0.000 description 5
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 4
- 239000003925 fat Substances 0.000 description 4
- 235000019197 fats Nutrition 0.000 description 4
- 235000021588 free fatty acids Nutrition 0.000 description 4
- 238000005809 transesterification reaction Methods 0.000 description 4
- 235000015112 vegetable and seed oil Nutrition 0.000 description 4
- 240000002791 Brassica napus Species 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000010775 animal oil Substances 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 235000003441 saturated fatty acids Nutrition 0.000 description 3
- 150000004671 saturated fatty acids Chemical class 0.000 description 3
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 3
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 3
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
- 244000068988 Glycine max Species 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000012512 characterization method Methods 0.000 description 2
- 230000000875 corresponding effect Effects 0.000 description 2
- 108010011222 cyclo(Arg-Pro) Proteins 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000004886 process control Methods 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000003908 quality control method Methods 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 150000003626 triacylglycerols Chemical class 0.000 description 2
- QNLZIZAQLLYXTC-UHFFFAOYSA-N 1,2-dimethylnaphthalene Chemical class C1=CC=CC2=C(C)C(C)=CC=C21 QNLZIZAQLLYXTC-UHFFFAOYSA-N 0.000 description 1
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical class CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 1
- ORILYTVJVMAKLC-UHFFFAOYSA-N Adamantane Natural products C1C(C2)CC3CC1CC2C3 ORILYTVJVMAKLC-UHFFFAOYSA-N 0.000 description 1
- 239000002028 Biomass Substances 0.000 description 1
- 235000014698 Brassica juncea var multisecta Nutrition 0.000 description 1
- 235000006008 Brassica napus var napus Nutrition 0.000 description 1
- 235000006618 Brassica rapa subsp oleifera Nutrition 0.000 description 1
- 244000188595 Brassica sinapistrum Species 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 239000004165 Methyl ester of fatty acids Substances 0.000 description 1
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 1
- OUBMGJOQLXMSNT-UHFFFAOYSA-N N-isopropyl-N'-phenyl-p-phenylenediamine Chemical compound C1=CC(NC(C)C)=CC=C1NC1=CC=CC=C1 OUBMGJOQLXMSNT-UHFFFAOYSA-N 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 150000001924 cycloalkanes Chemical class 0.000 description 1
- 150000001925 cycloalkenes Chemical class 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000002816 fuel additive Substances 0.000 description 1
- 238000000769 gas chromatography-flame ionisation detection Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 229940073769 methyl oleate Drugs 0.000 description 1
- FSWDLYNGJBGFJH-UHFFFAOYSA-N n,n'-di-2-butyl-1,4-phenylenediamine Chemical compound CCC(C)NC1=CC=C(NC(C)CC)C=C1 FSWDLYNGJBGFJH-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 230000010355 oscillation Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- PDEDQSAFHNADLV-UHFFFAOYSA-M potassium;disodium;dinitrate;nitrite Chemical compound [Na+].[Na+].[K+].[O-]N=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O PDEDQSAFHNADLV-UHFFFAOYSA-M 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000004451 qualitative analysis Methods 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001960 triggered effect Effects 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
- C10L1/02—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
-
- 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
- C10L1/02—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
- C10L1/026—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only for compression ignition
-
- 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
- G01N33/2829—Mixtures of fuels
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/10—Biofuels, e.g. bio-diesel
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T436/00—Chemistry: analytical and immunological testing
- Y10T436/12—Condition responsive control
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T436/00—Chemistry: analytical and immunological testing
- Y10T436/20—Oxygen containing
- Y10T436/200833—Carbonyl, ether, aldehyde or ketone containing
Definitions
- the invention provides methods for analyzing and optimizing biofuel compositions.
- Biodiesel is the name for a variety of ester-based oxygenated fuels made from vegetable oils, fats, greases, or other sources of triglycerides.
- Biodiesel is a nontoxic and biodegradable blendstock which may be blended with petroleum diesel provided relevant specifications are met. Biodiesel has been designated as an alternative fuel by the United States Department of Energy and the United States Department of Transportation, and is registered with the United States Environmental Protection Agency as a fuel and fuel additive.
- biodiesel is made from numerous different feedstocks (e.g. rapeseed oil and palm oil), including mixed feedstocks
- a finished fuel manufacturer is often not aware of the exact feedstock composition of a purchased biodiesel.
- Biodiesel is commonly referred to by its feedstock source (e.g. rapeseed methyl ester, palm oil methyl ester). Since the performance of a biodiesel depends upon the particular feedstock mixture from which it was produced, formulators are therefore often unable to predict how the biodiesel will perform in the finished fuel blend.
- biodiesel in the absence of accurate feedstock information, it can prove difficult to anticipate whether any given biodiesel will afford a performance advantage such as an improved cetane number, or will in fact suffer from a performance disadvantage (such as poor low-temperature operability) that might call for the addition of a performance enhancer.
- Lack of a reliable biodiesel compositional profile also complicates fuel formulators' efforts to design biodiesel blends that satisfy applicable regulatory standards such as ASTM D975, ASTM D7467 Standard Specification for Diesel Fuel Oil, Biodiesel Blend (B6 - B20), and EN590.
- ASTM D975 ASTM D7467 Standard Specification for Diesel Fuel Oil, Biodiesel Blend (B6 - B20), and EN590.
- the performance criteria and characteristics mandated by such standards are linked inextricably with a biodiesel's composition.
- Giordani, et ah "Identification of the Biodiesel Source Using an Electronic Nose", Energy & Fuels 2008, 22, 2743-2747, discloses the use of an e-nose and neural networks to identify a biodiesel feedstock source.
- Eide, et ah “Chemical Fingerprinting of Biodiesel Using Electrospray Mass Spectrometry and Chemometrics: Characterization, Discrimination, Identification, and Quantification in Petrodiesel, Energy & Fuels 2007, 21, 3702-3708, discloses the use of electrospray mass spectrometry (ESI-MS) to discriminate between biodiesel from different feedstocks and manufacturers, to identify fatty acid methyl esters (FAME) and free fatty acids, and to identify and quantify blend composition.
- ESI-MS electrospray mass spectrometry
- FAME fatty acid methyl esters
- Adam, et ah "Using comprehensive two-dimensional gas chromatography for the analysis of oxygenates in middle ditillates I.
- composition and feedstock source are not well-suited to control of biodiesel fuel blending.
- fatty acid alkyl esters e.g. rapeseed oil methyl ester (RME), soybean oil methyl ester (SME), palm oil methyl ester (PME), and tallow oil methyl ester (TME)
- RME rapeseed oil methyl ester
- SME soybean oil methyl ester
- PME palm oil methyl ester
- TEE tallow oil methyl ester
- the methods described herein optimize the composition of a fatty acid alkyl ester-containing biofuel (e.g. a biodiesel or biodiesel blend) and comprise:
- preprogrammed instructions (1) calculates one or more fatty acid alkyl ester mass percentage ratios and algorithmically determines the volumetric percentages of one or more fatty acid alkyl esters (e.g. RME, SME, PME, TME) in the component using the one or more fatty acid alkyl ester mass percentage ratios as algorithmic independent variables (2) correlates the one or more fatty acid alkyl ester volumetric percentages to fuel performance data and generates an output signal indicative of that correlation; and
- the methods described herein optimize the composition of a fatty acid alkyl ester-containing biofuel (e.g. a biodiesel or biodiesel blend) and comprise:
- the analyzer or the processor determines the total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters present in the component.
- the processor is a component of the analyzer.
- the processor calculates four or more fatty acid alkyl ester mass percentage ratios and algorithmically determines the volumetric percentages of four or more fatty acid alkyl esters in the fatty acid alkyl ester- containing component.
- the biofuel is a biodiesel or a biodiesel blend
- fatty acid alkyl ester volumetric percentages are correlated to reference biodiesel feedstock triglyceride (free fatty acid) profiles, and the feedstock of the biodiesel is thereby determined.
- the processor is a neural network which uses associative memory to generate algorithms that determine the volumetric percentages of the fatty acid alkyl esters.
- the analyzer measures the mass percentages in a biodiesel or a biodiesel component of a biodiesel blend of at least four alkyl esters of fatty acids selected from the group consisting of myristic acid (CI 4:0), palmitic acid (C16:0), palmitoleic acid (C16: l), stearic acid (C18:0), oleic acid (C18: l), linoleic acid (C18:2), linolenic acid (C18:3), eicosanoic acid (C20:0), eicosenoic acid (C20: l), docosanoic acid (C22:0), and docosenoic acid (C22: l).
- myristic acid CI 4:0
- palmitic acid C16:0
- palmitoleic acid C16: l
- stearic acid C18:0
- oleic acid C18: l
- the processor determines the volumetric percentage in a biodiesel or a biodiesel component of a biodiesel blend of one or more compositions selected from the group consisting of soybean oil alkyl ester, rapeseed oil alkyl ester, palm oil alkyl ester, canola oil alkyl ester, sunflower oil alkyl ester, olive oil alkyl ester, corn oil alkyl ester, tallow oil alkyl ester, coconut oil alkyl ester, jatropha oil alkyl ester, yellow grease alkyl ester, animal fat alkyl ester, used cooking oil alkyl ester, and mixtures thereof.
- the analyzer measures the mass percentages in a biodiesel or a biodiesel component of a biodiesel blend of methyl esters of palmitic acid (C16:0), palmitoleic acid (C16: l), oleic acid (C18: l cis 9) or oleic acid (C18: l trans 9), and linoleic acid (C18:2 cis 9, 12);
- the processor calculates the following mass percentage ratios: (1) linoleic acid methyl ester: oleic acid methyl ester (2) oleic acid methyl ester: palmitic acid methyl ester (3) palmitoleic acid methyl ester: palmitic acid methyl ester, and (4) palmitic acid methyl ester: oleic acid methyl ester (5) the ratios of the mass percentages of each of the at least two fatty acid alkyl esters and the total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters; and
- the processor determines the volumetric percentage in the biodiesel or biodiesel component of the biodiesel blend of soybean oil methyl ester (SME), rapeseed oil methyl ester (RME), tallow oil methyl ester (TME), palm oil methyl ester (PME), coconut oil methyl ester (CME), andjatropha oil methyl ester (JME) using either or both of the following two sets of algorithms:
- JME -2.034E-3 * (C18: l cis-9 to C18:3 cis-9,12,15) + 0.035 * (C18:2 cis-9,12 to C18:3 cis-9,12,15) - 0.026 * (poly to C18:3 cis-9,12,15)
- Mass percentages may be determined by any number of techniques that are well-known to those of ordinary skill in the art, including gas chromatography and other techniques described hereinafter. As explained in more detail hereinafter, the algorithmic determination of the volumetric percentages of the various vegetable and animal alkyl esters may be based on a statistical correlation of the known fatty acid alkyl ester profiles of vegetable and animal oil fatty acid alkyl esters and the determined ratios of the mass percentages of alkyl esters of fatty acids.
- formulators are able to ascertain accurately how a particular fatty acid alkyl ester profile of a biofuel (e.g. a biodiesel or a biodiesel blend) will affect fuel performance and can thereby optimize fuel design by varying as necessary the biofuel feedstock source or blended fuel components. For example, by knowing the fatty acid alkyl ester profile of a biodiesel or biodiesel component of a biodiesel blend, a finished fuel manufacturer is better able to utilize any performance advantage (e.g. cetane number improvement) and/or counter any performance disadvantage (e.g. poor low temperature operability) through appropriate use of additive(s).
- a performance advantage e.g. cetane number improvement
- counter any performance disadvantage e.g. poor low temperature operability
- refiners are also able to confirm whether a biofuel' s composition is consistent with specifications provided by the biofuel's supplier. They also can also employ optimal blending strategies (e.g. use of additives) that compensate for the use of more sustainable biomass (i.e. less food-source consuming) and/or less-expensive biofuel feedstock sources.
- Figure 1 and Figure 2 illustrate gas chromatographic analyses of the fatty acid alkyl ester profiles of vegetable and animal oil fatty acid alkyl esters, as determined or described in the experiment of Example 1 and Example 2, respectively.
- the gas chromatograph data in Figure 1 is raw and the gas chromatograph data in Figure 2 is normalized.
- Figures 3a, 3b, 3c and 3d present the fuel composition, fuel properties, and fuel fatty acid alkyl ester profile determined in Example 2.
- Figure 3a presents the base diesel fuel properties determined in Example 2.
- Figure 3b is the FAME Composition Calculator (fuel fatty acid alkyl ester profile) determined in Example 2.
- Figure 3c is the GC analysis of biodiesel samples determined in Example 2.
- Figure 3d is the IQT data determined in Example 2.
- a "fatty acid alkyl ester-containing biofuel” includes any fuel comprised of fatty acid alky esters made by the transesterification of a triglyceride with an alcohol.
- Fatty acid alkyl ester-containing biofuels include, but are not limited to, a biodiesel, a biodiesel blend, and a jet biofuel comprised of fatty acid alky esters.
- a “biodiesel” means a composition that can be used as a fuel for diesel engines and that contains at least about 50% by weight of esters of saturated and unsaturated fatty acids, including fatty acid methyl esters
- a biodiesel comprises between about 50% to about 99% by weight of methyl esters of saturated and unsaturated fatty acids, where the methyl esters of saturated and unsaturated fatty acids include C 8 -C 2 4 fatty acid methyl esters, where C 8 -C 24 indicates the number of carbons in the original fatty acid.
- Biodiesels can be made by transesterification of a triglyceride - containing feedstock with an alcohol, e.g. by transesterification of one or more vegetable oils, animal fats, algae-derived triglycerides, oils from halophytes, or mixtures thereof (e.g. transesterification of soybean oil, rapeseed oil, palm oil, canola oil, sunflower oil, olive oil, corn oil, tallow oil, coconut oil, jatropha oil, yellow grease, animal fats, used cooking oil, and mixtures thereof) with an alcohol such as methanol or ethanol.
- an alcohol such as methanol or ethanol.
- the fatty acid alkyl esters are largely unsaturated and comprise a rapeseed methyl ester, a canola methyl ester, a soybean methyl ester, a corn oil methyl ester, or a mixture thereof.
- a 100% biodiesel (B 100) should meet ASTM D6751 and/or EN 14214 or EN14213 specifications.
- Biodiesels can contain alkyl esters (e.g. methyl esters) of fatty acids such as myristic acid (CI 4:0), palmitic acid (CI 6:0), palmitoleic acid (CI 6: 1), stearic acid (C18:0), oleic acid (C18:l), linoleic acid (C18:2), linolenic acid (CI 8:3), eicosanoic acid (C20:0), eicosenoic acid (C20: l), docosanoic acid (C22:0), and docosenoic (or erucic) acid (C22: l).
- alkyl esters e.g. methyl esters
- fatty acids such as myristic acid (CI 4:0), palmitic acid (CI 6:0), palmitoleic acid (CI 6: 1), stearic acid (C18:0), oleic acid (C18:l), linoleic acid
- the fuel properties of biodiesel are determined by the amounts of each fatty acid in the feedstock used to produce the esters.
- Fatty acids are designated by two numbers: the first number denotes the total number of carbon atoms in the fatty acid chain and the second is the number of double bonds present in the chain.
- 18: 1 designates oleic acid, which has 18 carbon atoms and one double bond.
- the biofuel is a biodiesel or a biodiesel blend
- fatty acid alkyl ester volumetric percentages are correlated to reference biodiesel feedstock triglyceride profiles, and the feedstock of the biodiesel is thereby determined.
- fatty acid alkyl ester volumetric percentages are compared to known biodiesel feedstock triglyceride (free fatty acid) profiles such as those described in Catharino, et al., Energy & Fuels 2007, 21 , p. 3700, Table 1) and the biodiesel feedstock is identified.
- Biodiesel blends biodiesel blended with a petroleum distillate such as diesel fuel)(Bx) have a composition reflective of blend ratio and the distillate chosen for the blend.
- Petroleum distillate includes naphtha or middle distillates including kerosene and diesel.
- a non-limiting example of a “diesel fuel” or “a diesel” is composed of a mixture of C 9 -C 2 4 hydrocarbons that comprise about 50% to about 95% by volume of aliphatic hydrocarbons, of which about 0% to about 50% by volume are cycloparaffins, about 0% to about 5% by volume of olefinic hydrocarbons, and about 5% to about 50% by volume of aromatic hydrocarbons, and which boil at between about 280°F (138°C) and 750°F (399°C).
- a non-limiting example of a "kerosene” comprises about 5% to about 50% by volume of an aromatic fraction, about 0% to about 50% by volume of a cycloparaffm fraction, and about 0% to about 5% by volume of an olefinic fraction, with the rest comprising aliphatic hydrocarbons.
- An aromatics fraction can contain methyl aromatics and non-methyl alkyl aromatics.
- Non-limiting examples of non-methyl alkyl aromatics include molecules such as alkyl benzenes, dialkylbenzenes, alkylnaphthalenes, alkyl biphenyls, and alkyl phenanthrenes, and the like, in which one or more linear or branched alkyl groups containing two or more carbons is bonded to the aromatic ring.
- Non-limiting examples of methyl aromatics include aromatic molecules such as methylnaphthalene, dimethylnaphthalenes, and the like.
- a cycloparaffin fraction consists of cycloalkanes or molecules containing at least one cycloalkane ring.
- Non-limiting examples of components of the cycloparaffin fraction include alkylcyclohexanes and alky Icy clopentanes.
- An olefmic fraction can contain linear, branched, and cyclo-olefins.
- Non-limiting examples of components of the olefmic fraction include dodecenes and hexadecenes.
- a "cetane improver” includes but is not limited to 2-ethylhexyl nitrate (EHN) (e.g. HITEC® 4103, Ethyl Corp., Richmond, VA), cyclohexyl nitrate, di- tert-butyl peroxide, methyl nitrate, ethyl nitrate, n-propyl nitrate, isopropyl nitrate, allyl nitrate, n-butyl nitrate, isobutyl nitrate, sec-butyl nitrate, tert-butyl nitrate, n-amyl nitrate, isoamyl nitrate, 2-amyl nitrate, 3-amyl nitrate, tert-amyl nitrate, n-hexyl nitrate, 2-ethylhexyl nitrate, n-hept
- a biodiesel or biodiesel blend may also include an aromatic amine antioxidant (e.g. a phenylediamine- type antioxidant) such as N, N'-di-sec-butyl-p-phenylenediamine, 4-isopropylaminodiphenylamine, phenyl- naphthyl amine, and ring-alkylated diphenylamines.
- aromatic amine antioxidant e.g. a phenylediamine- type antioxidant
- a fatty acid alkyl ester-containing biofuel such as a biodiesel or biodiesel blend may also include performance additives such as cold flow additives, cloud point depressants, biocides, conductivity improvers, corrosion inhibitors, metal deactivators, and engine cleaning agents.
- performance additives such as cold flow additives, cloud point depressants, biocides, conductivity improvers, corrosion inhibitors, metal deactivators, and engine cleaning agents.
- such additives are present in an amount which ranges from about 0.001 to about 2.0% by weight of the fuel composition.
- “Fuel performance data” includes, but is not limited to, values indicative of lubricity, specific gravity, kinematic viscosity, flash point, boiling point, cetane number, cloud point, pour point, lubricity, low-temperature operability, and copper strip corrosion.
- Controlling blending of the biofuel in response to the processor output signal includes, but is not limited to, regulating the amount of cetane improver, antioxidant, or performance enhancer that is added to a biofuel, as well as controlling the amount of biodiesel, petroleum distillate, or petroleum- distillate-containing composition contained in a biodiesel blend or controlling the amount of a biodiesel blended with a jet fuel.
- Apparatus responsive to the processor output signal can be used to control blending, are well-known to those of ordinary skill in the art, and include, but are not limited to, process control devices and systems described hereinafter.
- the processor output signal may be transmitted electronically (e.g. wirelessly) from the processor to the apparatus or values indicative of the processor output signal may be entered into the apparatus manually or robotically using an appropriate interface.
- Mass percentages of alkyl esters of fatty acids may be determined by any number of analyzers, e.g. a gas chromatograph, a gas chromatography microchip, a gas-liquid chromatography microchip, a micro-gas chromatograph (GC), a mass spectrophotometer, a gas chromatograph -mass spectrophotometer, a liquid chromatograph- mass spectrophotometer, an ion mobility
- analyzers e.g. a gas chromatograph, a gas chromatography microchip, a gas-liquid chromatography microchip, a micro-gas chromatograph (GC), a mass spectrophotometer, a gas chromatograph -mass spectrophotometer, a liquid chromatograph- mass spectrophotometer, an ion mobility
- the analyzer is gas chromatograph or a gas chromatography microchip and the mass percentages in the sample of the at least four methyl esters of fatty acids are determined in accordance with EN- 14103.
- the total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters in the component are determined as follows.
- the total mass percentage of saturated fatty acid alkyl esters present in the component is determined by adding the mass percentages of those of the "at least two fatty acid alkyl esters" that are saturated fatty acid alkyl esters.
- the total mass percentage of monounsaturated fatty acid alkyl esters present in the component is determined by adding the mass percentages of those of the "at least two fatty acid alkyl esters" that are monounsaturated fatty acid alkyl esters.
- the total mass percentage of polyunsaturated fatty acid alkyl esters present in the component is determined by adding the mass percentages of those of the "at least two fatty acid alkyl esters" that are polyunsaturated fatty acid alkyl esters.
- the analyzer or processor can calculate such total mass percentages using hardware and software as described hereinafter or which is otherwise well- known to those of ordinary skill in the art.
- Ras of the mass percentage of each of the at least two fatty acid alkyl esters and the total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters are determined by dividing the mass percentage of each of the at least two fatty acid alkyl esters by (1) the mass percentage fatty acid alkyl esters (2) the mass percentage of monounsaturated fatty acid alkyl esters, and (3) the mass percentage of polyunsaturated fatty acid alkyl esters.
- "inputting values indicative of the at least two fatty acid alkyl ester mass percentages into a processor” includes transmitting a signal indicative of the fatty acid alkyl ester mass percentage measurements
- the analyzer and processor can be combined, e.g., the analyzer may include a processor as described herein. Values indicative of the total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters may be similarly inputted.
- Algorithms useful in determining fatty acid alkyl ester volumetric percentages may be derived from a statistical correlation of the determined ratios of the mass percentages of alkyl esters of fatty acids, or the determined ratios of the mass percentages of alkyl esters of fatty acids and the total mass percentages of fatty acid alkyl esters using a variety of statistical techniques. For example, principle component analysis/regression (PCA/PCR), partial least squares (PLS), and Gauss- Jordan row reduction may be used to derive algorithms that predict volumetric percentages of the various vegetable and animal alkyl esters based on determined ratios of the mass percentages of alkyl esters of fatty acids.
- PCA/PCR principle component analysis/regression
- PLS partial least squares
- Gauss- Jordan row reduction may be used to derive algorithms that predict volumetric percentages of the various vegetable and animal alkyl esters based on determined ratios of the mass percentages of alkyl esters of fatty acids.
- neural network may use associative memory to correlate fatty acid alkyl ester mass percentage ratios and volumetric
- Algorithms may be adjusted or confirmed as necessary by analyzing a sample of a fatty acid alkyl ester-containing biofuel to determine, e.g., the volumetric percentages of vegetable and animal oil fatty acid esters, comparing determined volumetric percentages with corresponding algorithmically-predicted volumetric percentages, and revising the algorithm through one or more of the mathematical techniques described above if differences between determined volumetric percentages and corresponding algorithmically-predicted volumetric percentages exceed an acceptable tolerance.
- the terms “predict” and “determine” are meant generally to encompass techniques or algorithms whose measurements or output fall within an acceptable range of error when compared to standardized methods (e.g., ASTM) of measuring the same property.
- An acceptable range of error may be within 15 percent, preferably within 10 percent, and more preferably 5 percent or less of the value measured by standardized methods (e.g., ASTM).
- ASTM standardized methods
- a programmable logic controller may be used as the processor which calculates the ratios of the mass percentages of the fatty acid alkyl esters and total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters and which performs one or more algorithms that determine fatty acid alkyl ester volumetric percentages.
- Programmable controllers are well- known to those of ordinary skill in the art and receive process inputs and adjust process parameters based on such inputs.
- Programmable controllers include but are not limited to electronic programmable logic controllers (PLC's) and personal computers.
- PLC's electronic programmable logic controllers
- Useful programmable logic controllers can include computer systems comprising central processing units (CPU's) for processing data, associated memory media including floppy disks or compact discs (CD's) which may store program instructions for CPU's, one or more display devices such as monitors, one or more alphanumeric input devices such as a keyboard, and one or more directional input devices such as a mouse.
- CPU's central processing units
- CD's compact discs
- display devices such as monitors
- alphanumeric input devices such as a keyboard
- directional input devices such as a mouse.
- Computer systems used as programmable logic controls can include a computational system memory such as DRAM, SRAM, EDO DRAM, SDRAM, DDR SDRAM, or Rambus RAM, or a non-volatile memory such as a magnetic media (e.g., a hard drive) or optical storage.
- the memory medium preferably stores a software program or programs for event-triggered transaction processing.
- the software program(s) may be implemented in any of various ways, including procedure- based techniques, component-based techniques, and/or object-oriented techniques, among others.
- Programmable controllers can, through hardwire or wireless transmission techniques that are well-known to those of ordinary skill in the art, may receive data, e.g. from apparatus that determine mass percentages of alkyl esters of fatty acids in a biodiesel feedstock sample, in order to implement the procedures described herein, e.g., to control the mixing of the biodiesel and the one or more additional components.
- Portions of the methods described herein can be applied as open loop or closed loop systems.
- Conventional PID (Proportional-Integrated-Derivative) controllers, DCS (distributed control systems), and other traditional control systems such as ratio controls and feed-forward controls can be applied to implement the methods described herein.
- Programmable logic controllers in the form of computer systems may take various forms, including a personal computer system, mainframe computer system, workstation, network appliance, Internet appliance or other device and encompass any device (or collection of devices) having a processor (or processors) which executes instructions from a memory medium.
- a memory medium (which may include a plurality of memory media) can store one or more software programs for performing various aspects of the methods that are predictive and used in control and optimization.
- the software program(s) can be implemented using component-based techniques and/or object-oriented techniques.
- the software program may be implemented using ActiveX controls, C++ objects, Java objects, Microsoft Foundation Classes (MFC), or other technologies or methodologies, as desired.
- a CPU such as the host CPU, executing code and data from the memory medium comprises a means for creating and executing the software program according to the methods described herein.
- one or more computer systems may implement one or more controllers.
- the methods described herein provide a method of optimizing the composition of a fuel comprising a mixture of a biodiesel or biodiesel blend and one or more additional components in which:
- UV-Vis ultraviolet-visible
- IR infrared
- spectrophotometer a UV fluorescence spectrophotometer, a mid-infrared (MIR) absorbance spectrophotometer, a near infrared
- XRF X-Ray fluorescence
- the fatty acid alkyl ester mass percentage measurements are transmitted to a programmable logic controller which:
- (1) calculates the following mass percentages ratios: (i) linoleic acid methyl ester: oleic acid methyl ester; (ii) oleic acid methyl ester: palmitic acid methyl ester; (iii) palmitoleic acid methyl ester: palmitic acid methyl ester; and (iv) palmitic acid methyl ester: oleic acid methyl ester;
- SME soybean oil methyl ester
- RME rapeseed oil methyl ester
- TME tallow oil methyl ester
- PME palm oil methyl ester
- Blends #1 through #8 The fatty acid methyl ester (FAME) profiles of thirty biodiesel samples were analyzed by gas chromatography. The resultant analyses of biodiesel composition by feedstock type were entered into a database and are presented in Figure 1. [0069] The following components were used to prepare Blends #1 through #8 below:
- Blend #1 SME / RME / TME / PME 25 /75/0/0 vol%) Blend #2 SME / RME / TME / PME (50/50/0/0 vol%) Blend #3 SME / RME / TME / PME (75 /25/0/0 vol%) Blend #4 SME / RME / TME / PME (25 / 25 / 25 / 25 vol%) Blend #5 SME / RME / TME / PME (40/30/20/ 10 vol%) Blend #6 ULSD / SME (80 / 20 vol%)
- Blend #7 ULSD / Blend #2 (80 / 20 vol%) (composition of the biodiesel being SME / RME / TME / PME (10/10/0/0 vol%)
- Blend #8 ULSD / Blend #4 (80 / 20 vol%) (composition of the biodiesel being SME / RME / TME / PME (5/5/5/5 vol%)
- Blends were analyzed by gas chromatography. For the biodiesel samples in the database and Blends #1 through #5 above, the ratios of the different methyl esters in each sample were calculated. This data was entered into a regression program (XLSTAT (Addinsoft, New York, New York)) and were used to generate the following prediction equations:
- Blend #1 SME / RME / TME / PME (27 / 66 / 7 / 0 vol%) Blend #2 SME / RME / TME / PME (52 / 46 / 2 / 0 vol%) Blend #3 SME / RME / TME / PME (73 / 25 / 0 / 2 vol%) Blend #4 SME / RME / TME / PME (51 / 10 / 13 / 26 vol%) Blend #5 SME / RME / TME / PME (54 / 18 / 20 / 8 vol%) Blend #6 SME / RME / TME / PME (18.3 / 1.4 / 0 / 0.3 vol%) Blend #7 SME / RME / TME / PME (10 / 9.8 / 0.6 / 0 vol%) Blend #8 SME / RME / TME / PME (10.8 / 2.2 / 2.6 / 4.4 vol%)
- Figures 3a, 3b, 3c and 3d present the fuel composition, fuel properties, and fuel fatty acid alkyl ester profile determined in Example 2.
- Figure 3a presents the base diesel fuel properties determined in Example 2.
- Figure 3b is the FAME Composition Calculator (fuel fatty acid alkyl ester profile) determined in Example 2.
- Figure 3c is the GC analysis of biodiesel samples determined in Example 2.
- Figure 3d is the IQT data determined in Example 2.
- To a base diesel fuel (with an ASTM D6890 derived cetane number of 46.8; Figure 3a) was added 10 vol% of a B100 sample (determined
- JME -2.034E-3 * (C18: l cis-9 to C18:3 cis-9,12,15) + 0.035 * (C18:2 cis-9,12 to C18:3 cis-9,12,15) - 0.026 * (poly to C18:3 cis-9,12,15)
- the U.S. (ASTM D975) and European (EN590) diesel fuel specifications differ with regard to cetane number.
- the D975 specification is 40 min compared to the EN590 specification of 51.0 min. Accordingly, consistent with fuel properties expected from the algorithmic determination of B100 fatty acid alkyl ester composition, blending of the B100 with the diesel yielded a fuel which satisfied EN590.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Food Science & Technology (AREA)
- Medicinal Chemistry (AREA)
- Physics & Mathematics (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Fats And Perfumes (AREA)
Abstract
The invention provides novel methods for optimizing the design of a fatty acid alkyl ester-containing biofuel (e.g. a biodiesel, a biodiesel blend, or a jet biofuel) and for identifying a fatty acid alkyl ester-containing biofuel's feedstock.
Description
METHODS FOR ANALYZING AND OPTIMIZING BIOFUEL
COMPOSITIONS
FIELD OF THE INVENTION
[0001] The invention provides methods for analyzing and optimizing biofuel compositions.
BACKGROUND OF THE INVENTION
[0002] Biodiesel is the name for a variety of ester-based oxygenated fuels made from vegetable oils, fats, greases, or other sources of triglycerides.
Biodiesel is a nontoxic and biodegradable blendstock which may be blended with petroleum diesel provided relevant specifications are met. Biodiesel has been designated as an alternative fuel by the United States Department of Energy and the United States Department of Transportation, and is registered with the United States Environmental Protection Agency as a fuel and fuel additive.
[0003] Because biodiesel is made from numerous different feedstocks (e.g. rapeseed oil and palm oil), including mixed feedstocks, a finished fuel manufacturer is often not aware of the exact feedstock composition of a purchased biodiesel. Biodiesel is commonly referred to by its feedstock source (e.g. rapeseed methyl ester, palm oil methyl ester). Since the performance of a biodiesel depends upon the particular feedstock mixture from which it was produced, formulators are therefore often unable to predict how the biodiesel will perform in the finished fuel blend. For example, in the absence of accurate feedstock information, it can prove difficult to anticipate whether any given biodiesel will afford a performance advantage such as an improved cetane number, or will in fact suffer from a performance disadvantage (such as poor low-temperature operability) that might call for the addition of a performance enhancer.
[0004] Lack of a reliable biodiesel compositional profile also complicates fuel formulators' efforts to design biodiesel blends that satisfy applicable regulatory standards such as ASTM D975, ASTM D7467 Standard Specification for Diesel Fuel Oil, Biodiesel Blend (B6 - B20), and EN590. The performance criteria and characteristics mandated by such standards are linked inextricably with a biodiesel's composition.
[0005] Giordani, et ah, "Identification of the Biodiesel Source Using an Electronic Nose", Energy & Fuels 2008, 22, 2743-2747, discloses the use of an e-nose and neural networks to identify a biodiesel feedstock source. Eide, et ah "Chemical Fingerprinting of Biodiesel Using Electrospray Mass Spectrometry and Chemometrics: Characterization, Discrimination, Identification, and Quantification in Petrodiesel, Energy & Fuels 2007, 21, 3702-3708, discloses the use of electrospray mass spectrometry (ESI-MS) to discriminate between biodiesel from different feedstocks and manufacturers, to identify fatty acid methyl esters (FAME) and free fatty acids, and to identify and quantify blend composition. Adam, et ah, "Using comprehensive two-dimensional gas chromatography for the analysis of oxygenates in middle ditillates I.
Determination of the nature of biodiesel blend in diesel fuel", J. Chromatogr. A 1 186 (2008) 236-244, discloses the use of two-dimensional gas chromatography (GC X GC) to quantify fatty acid esters in middle distillate hydrocarbons and individual identification and quantitation of fatty acid acid ester blends with diesel. Catharino, et ah, "Biodiesel Typification and Quality Control by Direct Infusion Electrospray Ionization Mass Spectrometry Fingerprinting", Energy & Fuels 2007, 21 , 3698-3701, discloses the use of ESI-MS for fingerprinting and quality control of biodiesels. Tiyapongpattana, et ah, "Characterization of biodiesel and biodiesel blends using comprehensive two-dimensional gas chromatography", J. Sep. Sci. 2008, 31 , 2640-2649, discloses a 2-D gas chromatography flame ionization detection method for biodiesel fuels.
[0006] The techniques cited in the above references do not provide readily programmable algorithmic techniques that correlate biodiesel FAME
composition and feedstock source, and therefore are not well-suited to control of biodiesel fuel blending.
[0007] Processes which seek to optimize fuel composition by analysis of the amount of biodiesel in a biodiesel blend, such as the processes described in U. S. Patent No. 7,404,41 1, fail to address the formulation problems mentioned above because they merely quantify the amount of biodiesel and do not provide any pre -blending qualitative analysis of biodiesel feedstock.
[0008] Accordingly, the need exists for methods which will accurately and conveniently analyze fatty acid alkyl ester-containing biofuels such as biodiesel, which will enable fuel formulators to optimize the design of fatty acid alkyl ester-containing biofuels, and which will facilitate the identification of a fatty acid alkyl ester-containing biofuel's feedstock.
SUMMARY OF THE INVENTION
[0009] We have discovered novel methods for optimizing the design of fatty acid alkyl ester-containing biofuels (e.g. a biodiesel or biodiesel blend) and for identifying a fatty acid alkyl ester-containing biofuel's feedstock.
[0010] In one aspect, the methods described herein accurately and
conveniently determine the volumetric percentages of fatty acid alkyl esters (e.g. rapeseed oil methyl ester (RME), soybean oil methyl ester (SME), palm oil methyl ester (PME), and tallow oil methyl ester (TME)) in a biodiesel or biodiesel component of a biodiesel blend and enable manufacturers to ascertain whether fuels made from the biodiesel or biodiesel blend will exhibit
performance advantages (e.g. improved cetane number) or disadvantages (e.g. poor low temperature operability) that will influence finished fuel specifications.
[0011] In one aspect, the methods described herein optimize the composition of a fatty acid alkyl ester-containing biofuel (e.g. a biodiesel or biodiesel blend) and comprise:
(a) submitting a sample of a fatty acid alkyl ester-containing component of the biofuel to an analyzer which measures the mass percentages in the component of at least two fatty acid alkyl esters (e.g. methyl oleate);
(b) inputting values indicative of the at least two fatty acid alkyl ester mass percentages into a processor which, in accordance with
preprogrammed instructions (1) calculates one or more fatty acid alkyl ester mass percentage ratios and algorithmically determines the volumetric percentages of one or more fatty acid alkyl esters (e.g. RME, SME, PME, TME) in the component using the one or more fatty acid alkyl ester mass percentage ratios as algorithmic independent variables (2) correlates the one or more fatty acid alkyl ester volumetric percentages to fuel performance data and generates an output signal indicative of that correlation; and
(c) controlling blending of the biofuel in response to the processor output signal.
[0012] In another aspect, the methods described herein optimize the composition of a fatty acid alkyl ester-containing biofuel (e.g. a biodiesel or biodiesel blend) and comprise:
(a) submitting a sample of a fatty acid alkyl ester-containing component of the biofuel to an analyzer which measures the mass percentages in the component of at least two fatty acid alkyl esters;
(b) determining total mass percentages of saturated,
monounsaturated, and polyunsaturated fatty acid alkyl esters in the component;
(c) inputting values indicative of (i) the at least two fatty acid alkyl ester mass percentages, and (ii) the total mass percentages of saturated,
monounsaturated, and polyunsaturated fatty acid alkyl esters into a processor which, in accordance with preprogrammed instructions (1) calculates (i) one or more fatty acid alkyl ester mass percentage ratios (ii) ratios of the mass percentage of each of the at least two fatty acid alkyl esters and the total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters (2) algorithmically determines the volumetric percentages of one or more fatty acid alkyl esters in the component using the one or more fatty acid alkyl ester mass percentage ratios, the total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters, and the ratios of the mass percentage of each of the at least two fatty acid alkyl esters and the total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters as algorithmic independent variables (4) correlates the one or more fatty acid alkyl ester volumetric percentages to fuel performance data and generates an output signal indicative of that correlation; and
(d) controlling blending of the biofuel in response to the processor output signal.
[0013] In certain aspects, the analyzer or the processor determines the total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters present in the component. In certain aspects, the processor is a component of the analyzer.
[0014] In one aspect, the processor calculates four or more fatty acid alkyl ester mass percentage ratios and algorithmically determines the volumetric percentages of four or more fatty acid alkyl esters in the fatty acid alkyl ester- containing component.
[0015] In certain aspects, the biofuel is a biodiesel or a biodiesel blend, fatty acid alkyl ester volumetric percentages are correlated to reference biodiesel
feedstock triglyceride (free fatty acid) profiles, and the feedstock of the biodiesel is thereby determined.
[0016] In certain aspects, the processor is a neural network which uses associative memory to generate algorithms that determine the volumetric percentages of the fatty acid alkyl esters.
[0017] In certain aspects, the analyzer measures the mass percentages in a biodiesel or a biodiesel component of a biodiesel blend of at least four alkyl esters of fatty acids selected from the group consisting of myristic acid (CI 4:0), palmitic acid (C16:0), palmitoleic acid (C16: l), stearic acid (C18:0), oleic acid (C18: l), linoleic acid (C18:2), linolenic acid (C18:3), eicosanoic acid (C20:0), eicosenoic acid (C20: l), docosanoic acid (C22:0), and docosenoic acid (C22: l).
[0018] In certain aspects, the processor determines the volumetric percentage in a biodiesel or a biodiesel component of a biodiesel blend of one or more compositions selected from the group consisting of soybean oil alkyl ester, rapeseed oil alkyl ester, palm oil alkyl ester, canola oil alkyl ester, sunflower oil alkyl ester, olive oil alkyl ester, corn oil alkyl ester, tallow oil alkyl ester, coconut oil alkyl ester, jatropha oil alkyl ester, yellow grease alkyl ester, animal fat alkyl ester, used cooking oil alkyl ester, and mixtures thereof.
[0019] For example, in one aspect of the methods described herein:
(a) the analyzer measures the mass percentages in a biodiesel or a biodiesel component of a biodiesel blend of methyl esters of palmitic acid (C16:0), palmitoleic acid (C16: l), oleic acid (C18: l cis 9) or oleic acid (C18: l trans 9), and linoleic acid (C18:2 cis 9, 12);
(b) the processor calculates the following mass percentage ratios: (1) linoleic acid methyl ester: oleic acid methyl ester (2) oleic acid methyl ester: palmitic acid methyl ester (3) palmitoleic acid methyl ester: palmitic acid methyl ester, and (4) palmitic acid methyl ester: oleic acid methyl ester (5) the ratios of
the mass percentages of each of the at least two fatty acid alkyl esters and the total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters; and
(c) the processor determines the volumetric percentage in the biodiesel or biodiesel component of the biodiesel blend of soybean oil methyl ester (SME), rapeseed oil methyl ester (RME), tallow oil methyl ester (TME), palm oil methyl ester (PME), coconut oil methyl ester (CME), andjatropha oil methyl ester (JME) using either or both of the following two sets of algorithms:
Set 1
(a) SME = 0.993 * (C18:2 cis-9, 12/C18: 1 cis-9)0 5 - 0.520
(b) RME = 0.089 * (C18: l cis-9/C16:0) - 0.104;
(c) TME = 86.671 * (CI 6: 1 cis-9/C16:0)2 - 0.030 ; and
(d) PME = 0.018 * (C16:0 / C18: l trans-9) - 0.069
Set 2
(a) TME = -0.053 + 0.219 * (C16: l cis-9) + 0.039 * (C16: l cis-9 to
C20:0)
(b) RME = -0.149 + 0.079 * (C18: l cis-9 to sats) + 0.019 * (C18: l cis-9 to C18:0)
(c) SME = -0.133 + 0.476 * (C18:2 cis-9,12 to C18: l cis-9)
(d) PME = -0.258 + 0.005 * (C16:0) + 0.094 * (C16:0 to C18:0)
(e) CME = 2.244E-8 + 0.835 * (C8:0 to C10:0)
(f) JME = -2.034E-3 * (C18: l cis-9 to C18:3 cis-9,12,15) + 0.035 * (C18:2 cis-9,12 to C18:3 cis-9,12,15) - 0.026 * (poly to C18:3 cis-9,12,15)
[0020] Mass percentages may be determined by any number of techniques that are well-known to those of ordinary skill in the art, including gas chromatography and other techniques described hereinafter. As explained in more detail hereinafter, the algorithmic determination of the volumetric
percentages of the various vegetable and animal alkyl esters may be based on a statistical correlation of the known fatty acid alkyl ester profiles of vegetable and animal oil fatty acid alkyl esters and the determined ratios of the mass percentages of alkyl esters of fatty acids.
[0021] Through use of the methods described herein, formulators are able to ascertain accurately how a particular fatty acid alkyl ester profile of a biofuel (e.g. a biodiesel or a biodiesel blend) will affect fuel performance and can thereby optimize fuel design by varying as necessary the biofuel feedstock source or blended fuel components. For example, by knowing the fatty acid alkyl ester profile of a biodiesel or biodiesel component of a biodiesel blend, a finished fuel manufacturer is better able to utilize any performance advantage (e.g. cetane number improvement) and/or counter any performance disadvantage (e.g. poor low temperature operability) through appropriate use of additive(s). By using the methods described herein, refiners are also able to confirm whether a biofuel' s composition is consistent with specifications provided by the biofuel's supplier. They also can also employ optimal blending strategies (e.g. use of additives) that compensate for the use of more sustainable biomass (i.e. less food-source consuming) and/or less-expensive biofuel feedstock sources.
[0022] Methods described herein provide a very good agreement between predicted and the actual compositions and their speed and economy prove well- suited for refinery operation.
[0023] These and other aspects are described further in the following detailed description of the invention.
BRIEF DESCRIPTION OF THE FIGURES
[0024] Figure 1 and Figure 2 illustrate gas chromatographic analyses of the fatty acid alkyl ester profiles of vegetable and animal oil fatty acid alkyl esters, as determined or described in the experiment of Example 1 and Example 2,
respectively. The gas chromatograph data in Figure 1 is raw and the gas chromatograph data in Figure 2 is normalized.
[0025] Figures 3a, 3b, 3c and 3d present the fuel composition, fuel properties, and fuel fatty acid alkyl ester profile determined in Example 2. Figure 3a presents the base diesel fuel properties determined in Example 2. Figure 3b is the FAME Composition Calculator (fuel fatty acid alkyl ester profile) determined in Example 2. Figure 3c is the GC analysis of biodiesel samples determined in Example 2. Figure 3d is the IQT data determined in Example 2.
DETAILED DESCRIPTION OF THE INVENTION
[0026] Unless otherwise stated, all percentages disclosed herein are on a volume basis.
[0027] Any end point of a range stated herein can be combined with any other end point to form another suitable range.
[0028] The following definitions apply unless indicated otherwise.
[0029] A "fatty acid alkyl ester-containing biofuel" includes any fuel comprised of fatty acid alky esters made by the transesterification of a triglyceride with an alcohol. Fatty acid alkyl ester-containing biofuels include, but are not limited to, a biodiesel, a biodiesel blend, and a jet biofuel comprised of fatty acid alky esters.
[0030] A "biodiesel" means a composition that can be used as a fuel for diesel engines and that contains at least about 50% by weight of esters of saturated and unsaturated fatty acids, including fatty acid methyl esters
(FAME's), fatty acid ethyl esters (FAEE's), propyl esters of fatty acids, or combinations of two or more methyl, ethyl, and propyl esters. In one example, a biodiesel comprises between about 50% to about 99% by weight of methyl esters of saturated and unsaturated fatty acids, where the methyl esters of saturated and
unsaturated fatty acids include C8-C24 fatty acid methyl esters, where C8-C24 indicates the number of carbons in the original fatty acid.
[0031] Biodiesels can be made by transesterification of a triglyceride - containing feedstock with an alcohol, e.g. by transesterification of one or more vegetable oils, animal fats, algae-derived triglycerides, oils from halophytes, or mixtures thereof (e.g. transesterification of soybean oil, rapeseed oil, palm oil, canola oil, sunflower oil, olive oil, corn oil, tallow oil, coconut oil, jatropha oil, yellow grease, animal fats, used cooking oil, and mixtures thereof) with an alcohol such as methanol or ethanol. In one aspect the fatty acid alkyl esters are largely unsaturated and comprise a rapeseed methyl ester, a canola methyl ester, a soybean methyl ester, a corn oil methyl ester, or a mixture thereof.
[0032] A 100% biodiesel (B 100) should meet ASTM D6751 and/or EN 14214 or EN14213 specifications.
[0033] Biodiesels can contain alkyl esters (e.g. methyl esters) of fatty acids such as myristic acid (CI 4:0), palmitic acid (CI 6:0), palmitoleic acid (CI 6: 1), stearic acid (C18:0), oleic acid (C18:l), linoleic acid (C18:2), linolenic acid (CI 8:3), eicosanoic acid (C20:0), eicosenoic acid (C20: l), docosanoic acid (C22:0), and docosenoic (or erucic) acid (C22: l). The fuel properties of biodiesel are determined by the amounts of each fatty acid in the feedstock used to produce the esters. Fatty acids are designated by two numbers: the first number denotes the total number of carbon atoms in the fatty acid chain and the second is the number of double bonds present in the chain. For example, 18: 1 designates oleic acid, which has 18 carbon atoms and one double bond.
[0034] The triglyceride or free fatty acid profiles of a number of common vegetable oils and animal fats are known. See e.g. Peterson, C.L., "Vegetable Oil as a Diesel Fuel: Status and Research Priorities," ASAE Transactions, V. 29, No. 5, Sep.-Oct. 1986, pp. 1413-1422.
[0035] As explained above, in certain aspects of the invention, the biofuel is a biodiesel or a biodiesel blend, fatty acid alkyl ester volumetric percentages are correlated to reference biodiesel feedstock triglyceride profiles, and the feedstock of the biodiesel is thereby determined. For example, fatty acid alkyl ester volumetric percentages are compared to known biodiesel feedstock triglyceride (free fatty acid) profiles such as those described in Catharino, et al., Energy & Fuels 2007, 21 , p. 3700, Table 1) and the biodiesel feedstock is identified.
[0036] Biodiesel blends (biodiesel blended with a petroleum distillate such as diesel fuel)(Bx)) have a composition reflective of blend ratio and the distillate chosen for the blend.
[0037] "Petroleum distillate" includes naphtha or middle distillates including kerosene and diesel.
[0038] A non-limiting example of a "diesel fuel" or "a diesel" is composed of a mixture of C9-C24 hydrocarbons that comprise about 50% to about 95% by volume of aliphatic hydrocarbons, of which about 0% to about 50% by volume are cycloparaffins, about 0% to about 5% by volume of olefinic hydrocarbons, and about 5% to about 50% by volume of aromatic hydrocarbons, and which boil at between about 280°F (138°C) and 750°F (399°C).
[0039] A non-limiting example of a "kerosene" comprises about 5% to about 50% by volume of an aromatic fraction, about 0% to about 50% by volume of a cycloparaffm fraction, and about 0% to about 5% by volume of an olefinic fraction, with the rest comprising aliphatic hydrocarbons.
[0040] An aromatics fraction can contain methyl aromatics and non-methyl alkyl aromatics. Non-limiting examples of non-methyl alkyl aromatics include molecules such as alkyl benzenes, dialkylbenzenes, alkylnaphthalenes, alkyl biphenyls, and alkyl phenanthrenes, and the like, in which one or more linear or
branched alkyl groups containing two or more carbons is bonded to the aromatic ring. Non-limiting examples of methyl aromatics include aromatic molecules such as methylnaphthalene, dimethylnaphthalenes, and the like.
[0041] A cycloparaffin fraction consists of cycloalkanes or molecules containing at least one cycloalkane ring. Non-limiting examples of components of the cycloparaffin fraction include alkylcyclohexanes and alky Icy clopentanes.
[0042] An olefmic fraction can contain linear, branched, and cyclo-olefins. Non-limiting examples of components of the olefmic fraction include dodecenes and hexadecenes.
[0043] A "cetane improver" includes but is not limited to 2-ethylhexyl nitrate (EHN) (e.g. HITEC® 4103, Ethyl Corp., Richmond, VA), cyclohexyl nitrate, di- tert-butyl peroxide, methyl nitrate, ethyl nitrate, n-propyl nitrate, isopropyl nitrate, allyl nitrate, n-butyl nitrate, isobutyl nitrate, sec-butyl nitrate, tert-butyl nitrate, n-amyl nitrate, isoamyl nitrate, 2-amyl nitrate, 3-amyl nitrate, tert-amyl nitrate, n-hexyl nitrate, 2-ethylhexyl nitrate, n-heptyl nitrate, sec-heptyl nitrate, n-octyl nitrate, sec-octyl nitrate, n-nonyl nitrate, n-decyl nitrate, n-dodecyl nitrate, cyclopentylnitrate, cyclohexylnitrate, methylcyclohexyl nitrate, isopropylcyclohexyl nitrate, and the esters of alkoxy substituted aliphatic alcohols, such as l-methoxypropyl-2-nitrate, 1 -ethoxpropyl-2 nitrate, 1- isopropoxy-butyl nitrate, 1-ethoxylbutyl nitrate, and mixtures thereof.
[0044] In one aspect, a biodiesel or biodiesel blend may also include an aromatic amine antioxidant (e.g. a phenylediamine- type antioxidant) such as N, N'-di-sec-butyl-p-phenylenediamine, 4-isopropylaminodiphenylamine, phenyl- naphthyl amine, and ring-alkylated diphenylamines.
[0045] A fatty acid alkyl ester-containing biofuel such as a biodiesel or biodiesel blend may also include performance additives such as cold flow additives, cloud point depressants, biocides, conductivity improvers, corrosion
inhibitors, metal deactivators, and engine cleaning agents. In some aspects, such additives are present in an amount which ranges from about 0.001 to about 2.0% by weight of the fuel composition.
[0046] "Fuel performance data" includes, but is not limited to, values indicative of lubricity, specific gravity, kinematic viscosity, flash point, boiling point, cetane number, cloud point, pour point, lubricity, low-temperature operability, and copper strip corrosion.
[0047] "Controlling blending of the biofuel in response to the processor output signal" includes, but is not limited to, regulating the amount of cetane improver, antioxidant, or performance enhancer that is added to a biofuel, as well as controlling the amount of biodiesel, petroleum distillate, or petroleum- distillate-containing composition contained in a biodiesel blend or controlling the amount of a biodiesel blended with a jet fuel. Apparatus responsive to the processor output signal can be used to control blending, are well-known to those of ordinary skill in the art, and include, but are not limited to, process control devices and systems described hereinafter.
[0048] In certain aspects, the processor output signal may be transmitted electronically (e.g. wirelessly) from the processor to the apparatus or values indicative of the processor output signal may be entered into the apparatus manually or robotically using an appropriate interface.
[0049] Mass percentages of alkyl esters of fatty acids may be determined by any number of analyzers, e.g. a gas chromatograph, a gas chromatography microchip, a gas-liquid chromatography microchip, a micro-gas chromatograph (GC), a mass spectrophotometer, a gas chromatograph -mass spectrophotometer, a liquid chromatograph- mass spectrophotometer, an ion mobility
spectrophotometer - mass spectrophotometer, an ultraviolet-visible (UV-Vis) absorbance spectrophotometer, an infrared (IR) absorbance spectrophotometer, a
UV fluorescence spectrophotometer, a mid-infrared (MIR) absorbance spectrophotometer, a near infrared ( R) absorbance spectrophotometer, a X- Ray fluorescence (XRF) spectrophotometer, a nuclear magnetic resonance spectrophotometer, a micro-oscillation spectrophotometer, micro-distillation- spectrophotometer, micro-mass spectrophotometer, or a micro-ion mobility spectrophotometer. In one aspect, the analyzer is gas chromatograph or a gas chromatography microchip and the mass percentages in the sample of the at least four methyl esters of fatty acids are determined in accordance with EN- 14103.
[0050] Details on the preparation of biodiesel samples and conducting gas chromatography runs on such samples are provided in the ASTM D6584 standard. See Biodiesel Analytical Methods August 2002- January 2004, July 2004 NREL/SR-510-36240.
[0051] The total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters in the component are determined as follows. The total mass percentage of saturated fatty acid alkyl esters present in the component is determined by adding the mass percentages of those of the "at least two fatty acid alkyl esters" that are saturated fatty acid alkyl esters. The total mass percentage of monounsaturated fatty acid alkyl esters present in the component is determined by adding the mass percentages of those of the "at least two fatty acid alkyl esters" that are monounsaturated fatty acid alkyl esters. The total mass percentage of polyunsaturated fatty acid alkyl esters present in the component is determined by adding the mass percentages of those of the "at least two fatty acid alkyl esters" that are polyunsaturated fatty acid alkyl esters. The analyzer or processor can calculate such total mass percentages using hardware and software as described hereinafter or which is otherwise well- known to those of ordinary skill in the art.
[0052] "Ratios of the mass percentage of each of the at least two fatty acid alkyl esters and the total mass percentages of saturated, monounsaturated, and
polyunsaturated fatty acid alkyl esters" are determined by dividing the mass percentage of each of the at least two fatty acid alkyl esters by (1) the mass percentage fatty acid alkyl esters (2) the mass percentage of monounsaturated fatty acid alkyl esters, and (3) the mass percentage of polyunsaturated fatty acid alkyl esters.
[0053] In certain aspects, "inputting values indicative of the at least two fatty acid alkyl ester mass percentages into a processor" includes transmitting a signal indicative of the fatty acid alkyl ester mass percentage measurements
electronically (e.g. wirelessly) from the analyzer to the processor or entering the values into the processor manually or robotically using an appropriate interface. The analyzer and processor can be combined, e.g., the analyzer may include a processor as described herein. Values indicative of the total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters may be similarly inputted.
[0054] Algorithms useful in determining fatty acid alkyl ester volumetric percentages may be derived from a statistical correlation of the determined ratios of the mass percentages of alkyl esters of fatty acids, or the determined ratios of the mass percentages of alkyl esters of fatty acids and the total mass percentages of fatty acid alkyl esters using a variety of statistical techniques. For example, principle component analysis/regression (PCA/PCR), partial least squares (PLS), and Gauss- Jordan row reduction may be used to derive algorithms that predict volumetric percentages of the various vegetable and animal alkyl esters based on determined ratios of the mass percentages of alkyl esters of fatty acids.
[0055] Artificial neural network techniques which have been used to model biodiesel manufacturing conditions and physical properties, see Rajendra, et al., "Prediction of optimized pretreatment process parameters for biodiesel production using ANN and GA", Fuel. Vol. 88, Issue 5 May 2009, pp. 868-875, Baroutian, et al., "Predication of Palm Oil-Based Methyl Ester Biodiesel Density
Using Artificial Neural Networks", Journal of Applied Sciences 8(10): 1938- 1943, 2008, may be adapted to derive the requisite algorithms through principles well-known to those of ordinary skill in the art.
[0056] Alternatively, through programming techniques well-known to those of ordinary skill in the art, neural network may use associative memory to correlate fatty acid alkyl ester mass percentage ratios and volumetric
percentages.
[0057] Algorithms may be adjusted or confirmed as necessary by analyzing a sample of a fatty acid alkyl ester-containing biofuel to determine, e.g., the volumetric percentages of vegetable and animal oil fatty acid esters, comparing determined volumetric percentages with corresponding algorithmically-predicted volumetric percentages, and revising the algorithm through one or more of the mathematical techniques described above if differences between determined volumetric percentages and corresponding algorithmically-predicted volumetric percentages exceed an acceptable tolerance.
[0058] As used herein the terms "predict" and "determine" are meant generally to encompass techniques or algorithms whose measurements or output fall within an acceptable range of error when compared to standardized methods (e.g., ASTM) of measuring the same property. An acceptable range of error may be within 15 percent, preferably within 10 percent, and more preferably 5 percent or less of the value measured by standardized methods (e.g., ASTM). Thus, where one measuring technique or algorithm has a range of error in excess of 15 percent of a standardized method, such a technique or algorithm would not be considered to be predictive or determinative of the property sought to be measured or otherwise ascertained. In contrast, where another measuring technique or algorithm has a range of error of 15 percent or less, then such a technique or algorithm would be considered to be predictive or determinative of the property sought to be measured or otherwise ascertained.
[0059] A programmable logic controller may be used as the processor which calculates the ratios of the mass percentages of the fatty acid alkyl esters and total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters and which performs one or more algorithms that determine fatty acid alkyl ester volumetric percentages. Programmable controllers are well- known to those of ordinary skill in the art and receive process inputs and adjust process parameters based on such inputs. Programmable controllers include but are not limited to electronic programmable logic controllers (PLC's) and personal computers. Useful programmable logic controllers can include computer systems comprising central processing units (CPU's) for processing data, associated memory media including floppy disks or compact discs (CD's) which may store program instructions for CPU's, one or more display devices such as monitors, one or more alphanumeric input devices such as a keyboard, and one or more directional input devices such as a mouse. Computer systems used as programmable logic controls can include a computational system memory such as DRAM, SRAM, EDO DRAM, SDRAM, DDR SDRAM, or Rambus RAM, or a non-volatile memory such as a magnetic media (e.g., a hard drive) or optical storage. The memory medium preferably stores a software program or programs for event-triggered transaction processing. The software program(s) may be implemented in any of various ways, including procedure- based techniques, component-based techniques, and/or object-oriented techniques, among others.
[0060] Programmable controllers (e.g., PLC's) can, through hardwire or wireless transmission techniques that are well-known to those of ordinary skill in the art, may receive data, e.g. from apparatus that determine mass percentages of alkyl esters of fatty acids in a biodiesel feedstock sample, in order to implement the procedures described herein, e.g., to control the mixing of the biodiesel and the one or more additional components.
[0061] Portions of the methods described herein can be applied as open loop or closed loop systems. Conventional PID (Proportional-Integrated-Derivative) controllers, DCS (distributed control systems), and other traditional control systems such as ratio controls and feed-forward controls can be applied to implement the methods described herein.
[0062] Programmable logic controllers in the form of computer systems may take various forms, including a personal computer system, mainframe computer system, workstation, network appliance, Internet appliance or other device and encompass any device (or collection of devices) having a processor (or processors) which executes instructions from a memory medium.
[0063] A memory medium (which may include a plurality of memory media) can store one or more software programs for performing various aspects of the methods that are predictive and used in control and optimization. The software program(s) can be implemented using component-based techniques and/or object-oriented techniques. For example, the software program may be implemented using ActiveX controls, C++ objects, Java objects, Microsoft Foundation Classes (MFC), or other technologies or methodologies, as desired. A CPU, such as the host CPU, executing code and data from the memory medium comprises a means for creating and executing the software program according to the methods described herein. In some embodiments, one or more computer systems may implement one or more controllers.
[0064] In one aspect, the methods described herein provide a method of optimizing the composition of a fuel comprising a mixture of a biodiesel or biodiesel blend and one or more additional components in which:
(a) the mass percentages of methyl esters of palmitic acid (CI 6:0), palmitoleic acid (C16: l), oleic acid (C18: l), and linoleic acid (C18:2) in the
biodiesel or biodiesel component of a biodiesel blend are measured using a gas chromatograph, a gas chromatography microchip, a gas-liquid chromatography microchip, a micro-gas chromatograph (GC), a mass spectrophotometer, a gas chromatograph -mass spectrophotometer, a liquid chromatograph- mass spectrophotometer, an ion mobility spectrophotometer - mass
spectrophotometer, an ultraviolet-visible (UV-Vis) absorbance spectrophotometer, an infrared (IR) absorbance
spectrophotometer, a UV fluorescence spectrophotometer, a mid-infrared (MIR) absorbance spectrophotometer, a near infrared
[0065] ( R) absorbance spectrophotometer, a X-Ray fluorescence (XRF) spectrophotometer, a nuclear magnetic resonance spectrophotometer, a micro- oscillation spectrophotometer, micro-distillation- spectrophotometer, micro-mass spectrophotometer, or a micro-ion mobility spectrophotometer;(b) the fatty acid alkyl ester mass percentage measurements are transmitted to a programmable logic controller which:
(1) calculates the following mass percentages ratios: (i) linoleic acid methyl ester: oleic acid methyl ester; (ii) oleic acid methyl ester: palmitic acid methyl ester; (iii) palmitoleic acid methyl ester: palmitic acid methyl ester; and (iv) palmitic acid methyl ester: oleic acid methyl ester;
(2) performs the following algorithms to determine the volumetric percentages of soybean oil methyl ester (SME), rapeseed oil methyl ester (RME), tallow oil methyl ester (TME), and palm oil methyl ester (PME) in the biodiesel or biodiesel component of a biodiesel blend:
(a) SME = 0.993 * (C18:2 cis-9, 12/C18: 1 cis-9)0 5 - 0.520;
(b) RME = 0.089 * (C18:l cis-9/C16:0) - 0.104;
(c) TME = 86.671 * (C16: l cis-9/C16:0)2 - 0.030; and
(d) PME = 0.018 * (C16:0 / C18: l trans-9) - 0.069;
(3) correlates the volumetric percentages of soybean oil methyl ester (SME), rapeseed oil methyl ester (RME), tallow oil methyl ester (TME), and palm oil methyl ester (PME) with programmed values for fuel performance data selected from the group consisting of lubricity, specific gravity, kinematic viscosity, flash point, boiling point, cetane number, cloud point, pour point, lubricity, and copper strip corrosion and generates an output signal indicative of that correlation;
(4) controls mixing of the biodiesel or biodiesel blend and one or more additional components selected from the group consisting of a petroleum distillate, a cetane improver, a performance additive, and an antioxidant in response to the processor output signal; and optionally
(5) correlates the volumetric percentages of soybean oil methyl ester (SME), rapeseed oil methyl ester (RME), tallow oil methyl ester (TME), and palm oil methyl ester (PME) to reference biodiesel feedstock triglyceride profiles and determines the biodiesel' s feedstock.
[0066] Those of ordinary skill in the art will appreciate that methods of the invention can be applied using a variety of well-known equipment and process control schemes.
[0067] These and other aspects of the invention are illustrated by the following example, which is illustrative only and is not limiting.
Example 1
[0068] The fatty acid methyl ester (FAME) profiles of thirty biodiesel samples were analyzed by gas chromatography. The resultant analyses of biodiesel composition by feedstock type were entered into a database and are presented in Figure 1.
[0069] The following components were used to prepare Blends #1 through #8 below:
Soybean Methyl Ester (SME) - Code #06-23754
Rapeseed Methyl Ester (RME) - Code #06-24237
Tallow Methyl Ester (TME) - Code #06-23646
Palm Oil Methyl Ester (PME) - Code #07-17170
ULSD - Code #03-57259.
[0070] The following blends were prepared.
Blend #1 SME / RME / TME / PME (25 /75/0/0 vol%) Blend #2 SME / RME / TME / PME (50/50/0/0 vol%) Blend #3 SME / RME / TME / PME (75 /25/0/0 vol%) Blend #4 SME / RME / TME / PME (25 / 25 / 25 / 25 vol%) Blend #5 SME / RME / TME / PME (40/30/20/ 10 vol%) Blend #6 ULSD / SME (80 / 20 vol%)
Blend #7 ULSD / Blend #2 (80 / 20 vol%) (composition of the biodiesel being SME / RME / TME / PME (10/10/0/0 vol%) Blend #8 ULSD / Blend #4 (80 / 20 vol%) (composition of the biodiesel being SME / RME / TME / PME (5/5/5/5 vol%)
[0071] The blends were analyzed by gas chromatography. For the biodiesel samples in the database and Blends #1 through #5 above, the ratios of the different methyl esters in each sample were calculated. This data was entered into a regression program (XLSTAT (Addinsoft, New York, New York)) and were used to generate the following prediction equations:
(a) SME = 0.993 * (CI 8:2 cis-9, 12/C18:1 cis-9)0.5 - 0.520
(b) RME = 0.089 * (C18:l cis-9/C16:0) - 0.104;
(c) TME = 86.671 * (C16:l cis-9/C16:0)2 - 0.030 ; and
(d) PME = 0.018 * (C16:0 / C18:l trans-9) - 0.069.
[0072] These equations were then used to predict the biodiesel feedstock composition of Blends #1 through #8. The results, normalized to 100 volume %, are reported below.
Blend #1 SME / RME / TME / PME (27 / 66 / 7 / 0 vol%) Blend #2 SME / RME / TME / PME (52 / 46 / 2 / 0 vol%) Blend #3 SME / RME / TME / PME (73 / 25 / 0 / 2 vol%) Blend #4 SME / RME / TME / PME (51 / 10 / 13 / 26 vol%) Blend #5 SME / RME / TME / PME (54 / 18 / 20 / 8 vol%) Blend #6 SME / RME / TME / PME (18.3 / 1.4 / 0 / 0.3 vol%) Blend #7 SME / RME / TME / PME (10 / 9.8 / 0.6 / 0 vol%) Blend #8 SME / RME / TME / PME (10.8 / 2.2 / 2.6 / 4.4 vol%)
[0073] The predicted fatty acid alkyl ester profiles of the biodiesels or biodiesel components of the biodiesel blends agreed very well with the actual fatty acid alkyl ester profiles of the biodiesels and biodiesel components of the biodiesel blends.
Example 2
[0074] The fatty acid methyl ester (FAME) profiles of forty two biodiesel samples were analyzed by gas chromatography. The resultant analyses of biodiesel composition by feedstock type were normalized and entered into a database and are presented in Figure 2.
[0075] Figures 3a, 3b, 3c and 3d present the fuel composition, fuel properties, and fuel fatty acid alkyl ester profile determined in Example 2. Figure 3a presents the base diesel fuel properties determined in Example 2. Figure 3b is the FAME Composition Calculator (fuel fatty acid alkyl ester profile) determined in Example 2. Figure 3c is the GC analysis of biodiesel samples determined in Example 2. Figure 3d is the IQT data determined in Example 2.
[0076] To a base diesel fuel (with an ASTM D6890 derived cetane number of 46.8; Figure 3a) was added 10 vol% of a B100 sample (determined
algorithmically (Figure 3 c) to comprise mostly PME). The resultant blend had an ASTM D6890 derived cetane number of 51.6. The following algorithms were used:
(a) TME = -0.053 + 0.219 * (C16: l cis-9) + 0.039 * (C16: l cis-9 to
C20:0)
(b) RME = -0.149 + 0.079 * (C18: l cis-9 to sats) + 0.019 * (C18: l cis-9 to C18:0)
(c) SME = -0.133 + 0.476 * (C18:2 cis-9,12 to C18: l cis-9)
(d) PME = -0.258 + 0.005 * (C16:0) + 0.094 * (C16:0 to C18:0)
(e) CME = 2.244E-8 + 0.835 * (C8:0 to C10:0)
(f) JME = -2.034E-3 * (C18: l cis-9 to C18:3 cis-9,12,15) + 0.035 * (C18:2 cis-9,12 to C18:3 cis-9,12,15) - 0.026 * (poly to C18:3 cis-9,12,15)
[0077] The U.S. (ASTM D975) and European (EN590) diesel fuel specifications differ with regard to cetane number. The D975 specification is 40 min compared to the EN590 specification of 51.0 min. Accordingly, consistent with fuel properties expected from the algorithmic determination of B100 fatty acid alkyl ester composition, blending of the B100 with the diesel yielded a fuel which satisfied EN590.
[0078] It is to be understood that the above description is intended for illustrative purposes only, and is not intended to limit the scope of the present invention in any way.
[0079] It is to be understood that the above description is intended for illustrative purposes only and is not intended to limit the scope of the present invention in any way.
Claims
1. A method of optimizing the composition of a biofuel comprised of fatty acid alkyl esters, the method comprising:
(a) submitting a sample of a fatty acid alkyl ester-containing component of the biofuel to an analyzer which measures the mass percentages in the component of at least two fatty acid alkyl esters;
(b) inputting values indicative of the at least two fatty acid alkyl ester mass percentages into a processor which, in accordance with preprogrammed instructions (1) calculates one or more fatty acid alkyl ester mass percentage ratios and algorithmically determines the volumetric
percentages of one or more fatty acid alkyl esters in the component using the one or more fatty acid alkyl ester mass percentage ratios as algorithmic independent variables (2) correlates the one or more fatty acid alkyl ester volumetric percentages to fuel performance data and generates an output signal indicative of that correlation; and
(c) controlling blending of the biofuel in response to the processor output signal.
2. The method of claim 1, wherein the processor calculates four or more fatty acid alkyl ester mass percentage ratios and algorithmically determines the volumetric percentages of four or more fatty acid alkyl esters.
3. The method of claim 1 , wherein:
(a) the analyzer is gas chromatograph, a gas chromatography microchip, a gas-liquid chromatography microchip, a micro-gas chromatograph (GC), a mass spectrophotometer, a gas chromatograph -mass spectrophotometer, a liquid chromatograph- mass spectrophotometer, an ion mobility
spectrophotometer - mass spectrophotometer, an ultraviolet-visible (UV-Vis) absorbance spectrophotometer, an infrared (IR) absorbance spectrophotometer, a UV fluorescence spectrophotometer, a mid-infrared (MIR) absorbance spectrophotometer, a near infrared ( R) absorbance spectrophotometer, a X- Ray fluorescence (XRF) spectrophotometer, a nuclear magnetic resonance spectrophotometer, a micro-oscillation spectrophotometer, micro-distillation- spectrophotometer, micro-mass spectrophotometer, or a micro-ion mobility spectrophotometer; and
(b) the processor is a programmable logic controller.
4. The method of claim 1, wherein the biofuel is a biodiesel or a biodiesel blend and the volumetric percentages of one or more fatty acid alkyl esters are correlated to reference biodiesel feedstock triglyceride profiles and the biodiesel' s feedstock, or the feedstock of the biodiesel component of the biodiesel blend, is thereby determined.
5. The method of claim 1, wherein the biofuel is a jet biofuel comprised of fatty acid alky esters.
6. The method of claim 1 , wherein the fuel performance data represents values indicative of properties selected from the group consisting of lubricity, specific gravity, kinematic viscosity, flash point, boiling point, cetane number, cloud point, pour point, lubricity, and copper strip corrosion.
7. The method of claim 1, wherein the biofuel is a biodiesel or biodiesel blend and the processor determines the volumetric percentage of one or more compositions selected from the group consisting of soybean oil alkyl ester, rapeseed oil alkyl ester, palm oil alkyl ester, canola oil alkyl ester, sunflower oil alkyl ester, olive oil alkyl ester, corn oil alkyl ester, tallow oil alkyl ester, coconut oil alkyl ester, jatropha oil alkyl ester, yellow grease alkyl ester, animal fat alkyl ester, and used cooking oil alkyl ester.
8. The method of claim 1, wherein the biofuel is a biodiesel or biodiesel blend and the analyzer measures the mass percentages of at least four alkyl esters of fatty acids selected from the group consisting of myristic acid (C14:0), palmitic acid (C16:0), palmitoleic acid (C16: l), stearic acid (C18:0), oleic acid (C18: l), linoleic acid (C18:2), linolenic acid (C18:3), eicosanoic acid (C20:0), eicosenoic acid (C20: l), docosanoic acid (C22:0), and docosenoic acid (C22: l).
9. The method of claim 1 , wherein the method further comprises:
(a) determining total mass percentages of saturated,
monounsaturated, and polyunsaturated fatty acid alkyl esters in the component; and
(b) inputting values indicative of the total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters into the processor which, in accordance with preprogrammed instructions (1) calculates (i) one or more fatty acid alkyl ester mass percentage ratios (ii) ratios of the mass percentage of each of the at least two fatty acid alkyl esters and the total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters (2) algorithmically determines the volumetric percentages of one or more fatty acid alkyl esters in the component using the one or more fatty acid alkyl ester mass percentage ratios, the total mass percentages of saturated,
monounsaturated, and polyunsaturated fatty acid alkyl esters, and ratios of the mass percentage of each of the at least two fatty acid alkyl esters and the total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters as algorithmic independent variables.
10. The method of claim 1 , wherein the method comprises:
(a) submitting a sample of a fatty acid alkyl ester-containing component of the biofuel to an analyzer which (1) measures the mass
percentages in the component of at least two fatty acid alkyl esters (2) contains a processor which, in accordance with preprogrammed instructions (i) calculates one or more fatty acid alkyl ester mass percentage ratios and algorithmically determines the volumetric percentages of one or more fatty acid alkyl esters in the component using the one or more fatty acid alkyl ester mass percentage ratios as algorithmic independent variables (ii) correlates the one or more fatty acid alkyl ester volumetric percentages to fuel performance data and generates an output signal indicative of that correlation; and
(b) controlling blending of the biofuel in response to the processor output signal.
1 1. The method of claim 1 , wherein one of or more compositions selected from the group consisting of a petroleum distillate, a cetane improver, a performance additive, and an antioxidant are blended with the biofuel in response to the processor output signal.
12. The method of claim 11 , wherein:
(a) the cetane improver is selected from the group consisting of 2-ethylhexyl nitrate, cyclohexyl nitrate, di-tert-butyl peroxide, methyl nitrate, ethyl nitrate, n-propyl nitrate, isopropyl nitrate, allyl nitrate, n-butyl nitrate, isobutyl nitrate, sec-butyl nitrate, tert-butyl nitrate, n-amyl nitrate, isoamyl nitrate, 2-amyl nitrate, 3-amyl nitrate, tert-amyl nitrate, n-hexyl nitrate, 2- ethylhexyl nitrate, n-heptyl nitrate, sec-heptyl nitrate, n-octyl nitrate, sec-octyl nitrate, n-nonyl nitrate, n-decyl nitrate, n-dodecyl nitrate, cyclopentylnitrate, cyclohexylnitrate, methylcyclohexyl nitrate, isopropylcyclohexyl nitrate, 1- methoxypropyl-2-nitrate, l-ethoxpropyl-2 nitrate, 1-isopropoxy -butyl nitrate,
1 -ethoxylbutyl nitrate, and mixtures thereof;
(b) the performance enhancer is selected from the group consisting of cold flow additives, cloud point depressants, biocides, conductivity improvers, corrosion inhibitors, metal deactivators, engine cleaning agents, and mixtures thereof; and (c) the antioxidant is selected from the group consisting of amine -based antioxidants, phenolic antioxidants, sulfur-based antioxidants, phosphorous-based antioxidants, zinc dithiophosphate, oil-soluble copper compounds, and mixtures thereof.
13. The method of claim 12, wherein:
(a) the biofuel is a biodiesel or biodiesel blend;
(b) the analyzer measures the mass percentages of methyl esters of palmitic acid (C16:0), palmitoleic acid (C16: l), oleic acid (C18: l), and linoleic acid (C18:2);
(c) the processor calculates the following mass percentage ratios: (1) linoleic acid methyl ester: oleic acid methyl ester; (2) oleic acid methyl ester: palmitic acid methyl ester; (3) palmitoleic acid methyl ester:
palmitic acid methyl ester; and (4) palmitic acid methyl ester: oleic acid methyl ester; and
(d) the processor determines the volumetric percentage of: (1) soybean oil methyl ester; (2) rapeseed oil methyl ester; (3) tallow oil methyl ester; and (4) palm oil methyl ester.
14. The method of claim 13, wherein
(a) the linoleic acid (C18:2) is linoleic acid (C18:2 cis 9, 12); and
(b) the oleic acid (CI 8: 1) is either oleic acid (CI 8: 1 cis 9) or oleic acid (CI 8: 1 trans 9).
15. The method of claim 14, wherein the processor determines the volumetric percentage of soybean oil methyl ester (SME), rapeseed oil methyl ester (RME), tallow oil methyl ester (TME), palm oil methyl ester (PME), coconut oil methyl ester (CME), and jatropha oil methyl ester (JME) either or both of the following two sets of algorithms:
Set 1
(a) SME = 0.993 * (C18:2 cis-9, 12/C18: 1 cis-9)0 5 - 0.520;
(b) RME = 0.089 * (C18: l cis-9/C16:0) - 0.104;
(c) TME = 86.671 * (C16: l cis-9/C16:0)2 - 0.030 ; and
(d) PME = 0.018 * (C16:0 / C18: l trans-9) - 0.069
Set 2
(a) TME = -0.053 + 0.219 * (C16: l cis-9) + 0.039 * (C16:l cis-9 to C20:0)
(b) RME = -0.149 + 0.079 * (C18: l cis-9 to sats) + 0.019 * (C18: l cis-9 to C18:0)
(c) SME = -0.133 + 0.476 * (C18:2 cis-9,12 to C18: l cis-9)
(d) PME = -0.258 + 0.005 * (C16:0) + 0.094 * (C16:0 to C18:0)
(e) CME = 2.244E-8 + 0.835 * (C8:0 to C10:0)
(f) JME = -2.034E-3 * (C18: l cis-9 to C18:3 cis-9,12,15) + 0.035 * (C18:2 cis-9,12 to C18:3 cis-9,12,15) - 0.026 * (poly to C18:3 cis-9,12,15).
16. The method of claim 15, wherein:
(a) the fuel performance data represents values indicative of properties selected from the group consisting of lubricity, specific gravity, kinematic viscosity, flash point, boiling point, cetane number, cloud point, pour point, lubricity, and copper strip corrosion; and
(b) blending of the biofuel and one or more additional compositions selected from the group consisting of a petroleum distillate, a cetane improver, a performance additive, and an antioxidant is controlled in response to the output signal.
17. The method of claim 16, wherein:
(a) the analyzer is gas chromatograph, a gas chromatography microchip, a gas-liquid chromatography microchip, a micro-gas chromatograph (GC), a mass spectrophotometer, a gas chromatograph -mass spectrophotometer, a liquid chromatograph- mass spectrophotometer, an ion mobility
spectrophotometer - mass spectrophotometer, an ultraviolet-visible (UV-Vis) absorbance spectrophotometer, an infrared (IR) absorbance spectrophotometer, a UV fluorescence spectrophotometer, a mid-infrared (MIR) absorbance spectrophotometer, a near infrared ( R) absorbance spectrophotometer, a X- Ray fluorescence (XRF) spectrophotometer, a nuclear magnetic resonance spectrophotometer, a micro-oscillation spectrophotometer, micro-distillation- spectrophotometer, micro-mass spectrophotometer, or a micro-ion mobility spectrometry; and
(b) the processor is a programmable logic controller.
18. The method of claim 17, wherein the biofuel is a biodiesel blend that comprises about 2% to about 98% by volume of a biodiesel and about 2% to about 98% by volume of a petroleum distillate.
19. A method of optimizing the composition of a biofuel comprised of fatty acid alkyl esters, the method comprising:
(a) submitting a sample of a fatty acid alkyl ester-containing component of the biofuel to an analyzer which measures the mass percentages in the component of at least two fatty acid alkyl esters;
(b) inputting values indicative of the at least two fatty acid alkyl ester mass percentages into a processor which (1) calculates one or more fatty acid alkyl ester mass percentage ratios and algorithmically determines the volumetric percentages of one or more fatty acid alkyl esters in the component using the one or more fatty acid alkyl ester mass percentage ratios as algorithmic independent variables (2) correlates the one or more fatty acid alkyl ester volumetric percentages to fuel performance data and generates an output signal indicative of that correlation; and
(c) controlling blending of the biofuel in response to the processor output signal, wherein the processor is a neural network which uses associative memory to generate algorithms that determine the volumetric percentages of one or more fatty acid alkyl esters.
20. The method of claim 19, wherein the method further comprises:
(a) determining total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters in the component; and
(b) inputting values indicative of the total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters into the processor which calculates one or more fatty acid alkyl ester mass percentage ratios and algorithmically determines the volumetric percentages of one or more fatty acid alkyl esters in the component using the one or more fatty acid alkyl ester mass percentage ratios, the total mass percentages of saturated,
monounsaturated, and polyunsaturated fatty acid alkyl esters, and and ratios of the mass percentage of each of the at least two fatty acid alkyl esters and the total mass percentages of saturated, monounsaturated, and polyunsaturated fatty acid alkyl esters as algorithmic independent variables.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP10838166.6A EP2513266A4 (en) | 2009-12-15 | 2010-12-13 | Methods for analyzing and optimizing biofuel compositions |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US28422309P | 2009-12-15 | 2009-12-15 | |
US61/284,223 | 2009-12-15 | ||
US12/963,663 US8586365B2 (en) | 2009-12-15 | 2010-12-09 | Methods for analyzing and optimizing biofuel compositions |
US12/963,663 | 2010-12-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2011075420A1 true WO2011075420A1 (en) | 2011-06-23 |
Family
ID=44141338
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2010/059985 WO2011075420A1 (en) | 2009-12-15 | 2010-12-13 | Methods for analyzing and optimizing biofuel compositions |
Country Status (3)
Country | Link |
---|---|
US (1) | US8586365B2 (en) |
EP (1) | EP2513266A4 (en) |
WO (1) | WO2011075420A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013066987A1 (en) * | 2011-11-04 | 2013-05-10 | Dexsil Corporation | System and method for the analysis of biodiesel |
US9797830B2 (en) | 2014-11-13 | 2017-10-24 | Emcee Electronics, Inc. | Biodiesel detector |
US9804086B2 (en) | 2014-11-13 | 2017-10-31 | Emcee Electronics, Inc. | Biodiesel detector |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8715374B2 (en) | 2011-01-06 | 2014-05-06 | Green Fuels Research, Ltd. | Methodology of post-transesterification processing of biodiesel resulting in high purity fame fractions and new fuels |
CN102626557B (en) * | 2012-04-13 | 2013-10-23 | 长春工业大学 | Molecular distillation process parameter optimizing method based on GA-BP (Genetic Algorithm-Back Propagation) algorithm |
US8911512B2 (en) | 2012-09-20 | 2014-12-16 | Kior, Inc. | Use of NIR spectra for property prediction of bio-oils and fractions thereof |
CA2886260A1 (en) * | 2012-11-16 | 2014-05-22 | Exxonmobil Research And Engineering Company | Methods and compositions for biodistillate fuels containing tallow esters and having low metals uptake |
CN105424539A (en) * | 2015-11-06 | 2016-03-23 | 中国科学院天津工业生物技术研究所 | Neural network-based method for predicting sugar yield produced through corn straw hydrolysis |
CN106841098B (en) * | 2016-07-29 | 2019-08-06 | 重庆医科大学 | It is a kind of to differentiate cis- and trans- geometric isomer near-infrared spectral analytical method |
WO2018148087A1 (en) | 2017-02-09 | 2018-08-16 | Texon Lp | Controlled blending of biodiesel into distillate streams |
US11578282B2 (en) | 2017-02-09 | 2023-02-14 | Texon Ip | Controlled blending of biodiesel into distillate streams |
US10324051B2 (en) | 2017-04-27 | 2019-06-18 | Petroleum Analyzer Company, Lp | Optical flash point detection on an automated open cup flash point detector |
US11186789B2 (en) * | 2017-07-18 | 2021-11-30 | Hull Partners, Llc | Biodiesel fuel mixtures |
US11306266B2 (en) | 2017-07-31 | 2022-04-19 | Hull Partners Llc | Biodiesel fuel mixtures |
CN109061021B (en) * | 2018-07-09 | 2021-02-26 | 西南民族大学 | Method for separating or analyzing phenolic acid compounds from burdock |
US11225611B1 (en) * | 2020-07-08 | 2022-01-18 | Exxonmobil Research And Engineering Company | Online analyzer for biofuel production |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20080172187A1 (en) * | 2006-12-22 | 2008-07-17 | Paradigm Sensors, Llc | Impedance spectroscopy (is) methods and systems for characterizing fuel |
US7404411B2 (en) * | 2005-03-23 | 2008-07-29 | Marathon Ashland Petroleum Llc | Method and apparatus for analysis of relative levels of biodiesel in fuels by near-infrared spectroscopy |
US20080256848A1 (en) * | 2007-04-19 | 2008-10-23 | Brennan Timothy J | Middle distillate fuels with a sustained conductivity benefit |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2483057C2 (en) * | 2006-06-28 | 2013-05-27 | Ньюселис Инк. | Fatty acid mixtures and use thereof |
US20080176885A1 (en) | 2006-10-10 | 2008-07-24 | University Of Kentucky | Novel synergistic opioid-cannabinoid codrug for pain management |
US20090316139A1 (en) | 2006-10-12 | 2009-12-24 | Dev Sagar Shrestha | Biodiesel/diesel blend level detection using absorbance |
-
2010
- 2010-12-09 US US12/963,663 patent/US8586365B2/en not_active Expired - Fee Related
- 2010-12-13 WO PCT/US2010/059985 patent/WO2011075420A1/en active Application Filing
- 2010-12-13 EP EP10838166.6A patent/EP2513266A4/en not_active Withdrawn
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7404411B2 (en) * | 2005-03-23 | 2008-07-29 | Marathon Ashland Petroleum Llc | Method and apparatus for analysis of relative levels of biodiesel in fuels by near-infrared spectroscopy |
US20080172187A1 (en) * | 2006-12-22 | 2008-07-17 | Paradigm Sensors, Llc | Impedance spectroscopy (is) methods and systems for characterizing fuel |
US20080256848A1 (en) * | 2007-04-19 | 2008-10-23 | Brennan Timothy J | Middle distillate fuels with a sustained conductivity benefit |
Non-Patent Citations (3)
Title |
---|
BAMGBOYE ET AL.: "Prediction of cetane number of biodiesel fuel from the fatty acid methyl ester (FAME) composition", INT. AGROPHYSICS, vol. 22, 2008, pages 21 - 29 * |
RAJENDRA ET AL.: "Prediction of optimized pretreatment process parameters for biodiesel production using ANN and GA", FUEL, vol. 88, 3 January 2009 (2009-01-03), pages 868 - 875, XP025915175, DOI: doi:10.1016/j.fuel.2008.12.008 * |
See also references of EP2513266A4 * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013066987A1 (en) * | 2011-11-04 | 2013-05-10 | Dexsil Corporation | System and method for the analysis of biodiesel |
US8709815B2 (en) | 2011-11-04 | 2014-04-29 | Dexsil Corporation | System and method for the analysis of biodiesel |
US9797830B2 (en) | 2014-11-13 | 2017-10-24 | Emcee Electronics, Inc. | Biodiesel detector |
US9804086B2 (en) | 2014-11-13 | 2017-10-31 | Emcee Electronics, Inc. | Biodiesel detector |
Also Published As
Publication number | Publication date |
---|---|
US8586365B2 (en) | 2013-11-19 |
EP2513266A4 (en) | 2014-01-01 |
US20110138679A1 (en) | 2011-06-16 |
EP2513266A1 (en) | 2012-10-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US8586365B2 (en) | Methods for analyzing and optimizing biofuel compositions | |
El-Araby et al. | Study on the characteristics of palm oil–biodiesel–diesel fuel blend | |
Bezergianni et al. | Comparison between different types of renewable diesel | |
Caldeira et al. | Fatty acid based prediction models for biodiesel properties incorporating compositional uncertainty | |
Lapuerta et al. | Key properties and blending strategies of hydrotreated vegetable oil as biofuel for diesel engines | |
Sivaramakrishnan et al. | Determination of cetane number of biodiesel and its influence on physical properties | |
Llamas et al. | Biokerosene from coconut and palm kernel oils: Production and properties of their blends with fossil kerosene | |
Gülüm et al. | A comprehensive study on measurement and prediction of viscosity of biodiesel-diesel-alcohol ternary blends | |
Tan et al. | Particle number emissions from a light-duty diesel engine with biodiesel fuels under transient-state operating conditions | |
Knothe | A comprehensive evaluation of the cetane numbers of fatty acid methyl esters | |
Gopinath et al. | Effects of the properties and the structural configurations of fatty acid methyl esters on the properties of biodiesel fuel: a review | |
WANG et al. | Influence of fatty acid composition of woody biodiesel plants on the fuel properties | |
Lin et al. | Profit and policy implications of producing biodiesel–ethanol–diesel fuel blends to specification | |
Islam et al. | Investigation of the effects of the fatty acid profile on fuel properties using a multi-criteria decision analysis | |
Kannan et al. | Studies on biodiesel production and its effect on DI diesel engine performance, emission and combustion characteristics | |
Ashraful et al. | Study of the effect of storage time on the oxidation and thermal stability of various biodiesels and their blends | |
Mofijur et al. | Assessment of physical, chemical, and tribological properties of different biodiesel fuels | |
Dwivedi et al. | Optimization of storage stability for Karanja biodiesel using box–Behnken design | |
Santos et al. | Cold flow properties: Applying exploratory analyses and assessing predictive methods for biodiesel and diesel-biodiesel blends | |
Kaisan et al. | Physico-chemical properties of bio-diesel from wild grape seeds oil and petro-diesel blends | |
Santhosh et al. | Poultry fat biodiesel as a fuel substitute in diesel-ethanol blends for DI-CI engine: Experimental, modeling and optimization | |
Masera et al. | Production, characterisation and assessment of biomixture fuels for compression ignition engine application | |
Górski et al. | Selected physicochemical properties of diethyl ether/rapeseed oil blends and their impact on diesel engine smoke opacity | |
Atgur et al. | Thermogravimetric and combustion efficiency analysis of Jatropha curcas biodiesel and its derivatives | |
Lapuerta et al. | Blending scenarios for soybean oil derived biofuels with conventional diesel |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 10838166 Country of ref document: EP Kind code of ref document: A1 |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 10838166 Country of ref document: EP Kind code of ref document: A1 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2010838166 Country of ref document: EP |