JP5053796B2 - Fuel oil composition for diesel engines - Google Patents
Fuel oil composition for diesel engines Download PDFInfo
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- JP5053796B2 JP5053796B2 JP2007277283A JP2007277283A JP5053796B2 JP 5053796 B2 JP5053796 B2 JP 5053796B2 JP 2007277283 A JP2007277283 A JP 2007277283A JP 2007277283 A JP2007277283 A JP 2007277283A JP 5053796 B2 JP5053796 B2 JP 5053796B2
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- fatty acid
- acid alkyl
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- oil composition
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- 239000000295 fuel oil Substances 0.000 title claims description 72
- 239000000203 mixture Substances 0.000 title claims description 71
- 239000000194 fatty acid Substances 0.000 claims description 62
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 61
- 229930195729 fatty acid Natural products 0.000 claims description 61
- 239000003921 oil Substances 0.000 claims description 51
- 235000019198 oils Nutrition 0.000 claims description 51
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 22
- 238000004821 distillation Methods 0.000 claims description 18
- 125000003118 aryl group Chemical group 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 13
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 9
- 239000008158 vegetable oil Substances 0.000 claims description 9
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 8
- 229920006395 saturated elastomer Polymers 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- 239000011593 sulfur Substances 0.000 claims description 8
- 239000002699 waste material Substances 0.000 claims description 8
- 239000003925 fat Substances 0.000 claims description 7
- 239000010775 animal oil Substances 0.000 claims description 6
- 150000003626 triacylglycerols Chemical class 0.000 claims description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 4
- 239000008162 cooking oil Substances 0.000 claims description 4
- 239000002994 raw material Substances 0.000 claims description 4
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims description 4
- 239000010779 crude oil Substances 0.000 claims description 3
- 241000592335 Agathis australis Species 0.000 claims description 2
- 239000013078 crystal Substances 0.000 description 31
- 238000001556 precipitation Methods 0.000 description 29
- 239000000446 fuel Substances 0.000 description 28
- 239000002585 base Substances 0.000 description 24
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
- 238000003860 storage Methods 0.000 description 16
- 238000000034 method Methods 0.000 description 15
- 238000012360 testing method Methods 0.000 description 14
- 230000000052 comparative effect Effects 0.000 description 12
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 11
- 125000005456 glyceride group Chemical group 0.000 description 10
- 239000013618 particulate matter Substances 0.000 description 10
- 239000000654 additive Substances 0.000 description 8
- 239000007789 gas Substances 0.000 description 8
- 238000002156 mixing Methods 0.000 description 8
- 238000002485 combustion reaction Methods 0.000 description 7
- 239000002283 diesel fuel Substances 0.000 description 7
- 238000004458 analytical method Methods 0.000 description 6
- 235000019197 fats Nutrition 0.000 description 6
- 150000004665 fatty acids Chemical class 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 238000004448 titration Methods 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 125000005907 alkyl ester group Chemical group 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 238000002425 crystallisation Methods 0.000 description 4
- 230000008025 crystallization Effects 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 230000003993 interaction Effects 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- -1 diglycerides Chemical class 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 238000004128 high performance liquid chromatography Methods 0.000 description 3
- 239000011259 mixed solution Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
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- 102000004882 Lipase Human genes 0.000 description 2
- 108090001060 Lipase Proteins 0.000 description 2
- 235000021360 Myristic acid Nutrition 0.000 description 2
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 2
- 235000021314 Palmitic acid Nutrition 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 239000003377 acid catalyst Substances 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 2
- 239000003225 biodiesel Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 239000012159 carrier gas Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 239000008157 edible vegetable oil Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000002828 fuel tank Substances 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N n-hexadecanoic acid Natural products CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 235000014593 oils and fats Nutrition 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 125000003367 polycyclic group Chemical group 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 101710134784 Agnoprotein Proteins 0.000 description 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
- 208000016444 Benign adult familial myoclonic epilepsy Diseases 0.000 description 1
- 239000002028 Biomass Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- 241000221089 Jatropha Species 0.000 description 1
- 239000004367 Lipase Substances 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000005233 alkylalcohol group Chemical group 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- 239000007857 degradation product Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- KZNICNPSHKQLFF-UHFFFAOYSA-N dihydromaleimide Natural products O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 208000016427 familial adult myoclonic epilepsy Diseases 0.000 description 1
- 235000019387 fatty acid methyl ester Nutrition 0.000 description 1
- ZGNITFSDLCMLGI-UHFFFAOYSA-N flubendiamide Chemical compound CC1=CC(C(F)(C(F)(F)F)C(F)(F)F)=CC=C1NC(=O)C1=CC=CC(I)=C1C(=O)NC(C)(C)CS(C)(=O)=O ZGNITFSDLCMLGI-UHFFFAOYSA-N 0.000 description 1
- 239000002816 fuel additive Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000010813 internal standard method Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 235000019421 lipase Nutrition 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
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- 238000002844 melting Methods 0.000 description 1
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- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
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- 239000002904 solvent Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
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- 239000000126 substance Substances 0.000 description 1
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Landscapes
- Liquid Carbonaceous Fuels (AREA)
Description
本発明は、ディーゼルエンジン用燃料油組成物に関する。更に詳しくは、曇り点以上の温度での貯蔵における燃料油中への結晶析出が抑制された、脂肪酸アルキルエステルの混合されているディーゼルエンジン用燃料油組成物に関する。 The present invention relates to a fuel oil composition for a diesel engine. More specifically, the present invention relates to a fuel oil composition for a diesel engine in which fatty acid alkyl ester is mixed, in which crystal precipitation in the fuel oil during storage at a temperature higher than the cloud point is suppressed.
近年、地球温暖化問題に対応するため、自動車より排出されるCO2を削減すべく、ハイブリット車等に代表されるような燃費改善によるCO2削減のための新技術の開発・導入が盛んに行われている。CO2削減の取組みは、自動車業界のみならず、石油業界でも盛んに行われており、特に二酸化炭素削減プロトコル、いわゆる京都議定書において、CO2排出がゼロカウントとされるバイオマス由来の燃料を代替燃料として用いることが検討されている。その中でもバイオディーゼル燃料は、ガソリンエンジンに対するディーゼルエンジンの熱効率の優位性(CO2排出量の優位性)、ならびに植物油を原料とすることから、再生可能なエネルギー源であること、廃食用油などの廃棄物を燃料に変換できることから、廃棄物削減が可能となることなどの特徴も相俟って、社会的な注目度もかなり高まってきている。 In recent years, in order to cope with the global warming problem, in order to reduce CO 2 emitted from automobiles, development and introduction of new technologies for reducing CO 2 by improving fuel consumption, such as hybrid cars, have been actively performed. Has been done. Efforts to reduce CO 2 are being actively pursued not only in the automobile industry but also in the oil industry. In particular, the CO 2 emission protocol, the so-called Kyoto Protocol, substitutes biomass-derived fuel for which CO 2 emissions are zero count. It is considered to be used as. Among them, biodiesel fuel is a renewable energy source because it is superior in the thermal efficiency of diesel engines (advantage of CO 2 emissions) over gasoline engines, and is made from vegetable oil. Since it is possible to convert waste into fuel, combined with features such as the ability to reduce waste, social attention has increased considerably.
しかしながら、現在のバイオディーゼル燃料の主流である、種々の動植物油又は廃食油の油脂をアルキルエステル化して得られる脂肪酸アルキルエステル燃料には、様々な問題が存在する。 However, there are various problems in the fatty acid alkyl ester fuel obtained by alkyl esterifying oils and fats of various animal and vegetable oils or waste cooking oil, which is the mainstream of current biodiesel fuel.
例えば、含有する脂肪酸アルキルエステルの組成が、飽和脂肪酸アルキルエステルを多く含むものの場合、低温性能に劣り、冬季などの低温環境下で使用する際にはディーゼル車の燃料ラインなどに設置されているフィルターを閉塞させるためエンジンへの燃料供給を阻害し、正常な運転を妨げる可能性がある。 For example, if the composition of fatty acid alkyl ester contains a large amount of saturated fatty acid alkyl ester, the low temperature performance is inferior, and when used in a low temperature environment such as winter, a filter installed in the fuel line of a diesel vehicle, etc. May block the fuel supply to the engine and hinder normal operation.
また、含有する脂肪酸アルキルエステルの組成が、不飽和脂肪酸アルキルエステルを多く含むものの場合、上記飽和脂肪酸アルキルエステルを多く含むものの場合と異なり、軽油と遜色ない低温性能を有するものもあるが、熱や光による分解・重合が起こりやすくなり、夏季などの高温環境下や、エンジンからの輻射熱により燃料温度が著しく高くなる場合には、不飽和脂肪酸アルキルエステル由来の分解物・重合物によりトラブルを発生する可能性がある。 In addition, in the case where the composition of the fatty acid alkyl ester contains a large amount of unsaturated fatty acid alkyl ester, unlike those containing a large amount of the saturated fatty acid alkyl ester, there are those having low temperature performance comparable to diesel oil, Decomposition / polymerization due to light is likely to occur, and in the high temperature environment such as summer, or when the fuel temperature becomes extremely high due to radiant heat from the engine, troubles may occur due to degradation products / polymers derived from unsaturated fatty acid alkyl esters. there is a possibility.
更に、脂肪酸アルキルエステル製造の原料となる動植物油又は廃食油の油脂が、アルキルエステル製造時に未反応、もしくは反応が不完全であるため残留するトリグリセリドやジグリセリド、モノグリセリドなどの脂肪酸グリセリドや、トリグリセリドのアルキルエステル化が完全になされた際に生成するグリセリン、脂肪酸アルキルエステル製造プロセスで使用されるアルキルアルコール、触媒として用いられるカリウムなどのアルカリ金属類は、燃料タンクや、燃料ライン、更にはエンジン部材に対し悪影響をもたらすため、軽油代替燃料としての使用に関しては、燃料性状のみならず、様々な品質項目において注視が必要であり、単純なる軽油代替燃料としての使用は好ましくない。 Furthermore, fatty acids such as triglycerides, diglycerides, monoglycerides and the like, and fatty acid glycerides such as triglycerides, diglycerides and monoglycerides remaining after the fats and oils of animal and vegetable oils or waste edible oils, which are raw materials for fatty acid alkyl ester production, are unreacted or incompletely reacted at the time of alkyl ester production. Alkaline metals such as glycerin produced when esterification is completely completed, alkyl alcohol used in the fatty acid alkyl ester production process, and potassium used as a catalyst are used for fuel tanks, fuel lines, and engine parts. Since it causes an adverse effect, it is necessary to pay attention not only to the fuel properties but also to various quality items regarding use as a light oil substitute fuel, and use as a simple light oil substitute fuel is not preferable.
このような脂肪酸アルキルエステル燃料を使用するにあたり、上記したような脂肪酸アルキルエステル燃料の懸念材料を払拭するため、種々の添加剤(BDF用低温流動性向上剤、酸化防止剤等)の開発や、軽油への混合使用に関する技術検討が進められてきた。特に軽油へ適宜混合し使用する方法は、盛んに検討されており(例えば、特許文献1、特許文献2参照)、脂肪酸アルキルエステルの軽油への混合は、脂肪酸アルキルエステル単独で使用した場合に比べCO2削減の観点からは若干劣るものの、燃料品質を維持しつつ、かつCO2削減も可能となる最も現実的な利用法といえる。 In using such a fatty acid alkyl ester fuel, development of various additives (low temperature fluidity improver for BDF, antioxidant, etc.) Technical studies on mixing and use in light oil have been promoted. In particular, methods of appropriately mixing and using light oil have been studied actively (see, for example, Patent Document 1 and Patent Document 2), and the mixing of fatty acid alkyl esters with light oil is more than when using fatty acid alkyl esters alone. although slightly inferior in terms of CO 2 reduction, while maintaining the fuel quality, and be the most practical usage for CO 2 reduction also becomes possible.
上記のような技術的背景から、脂肪酸アルキルエステルは軽油へ混合することにより、それ自体の低温性能・安定性・精製度の問題を薄めることが可能となり、かつ、5%以下の低濃度の混合であれば、ほぼ問題ないレベルとできることが明らかになった。
ところで、本発明者らも、上記のような脂肪酸アルキルエステルの軽油混合利用を検討していたが、その際に、脂肪酸アルキルエステル混合軽油組成物において、脂肪酸アルキルエステル由来の結晶が冬季には十分達し得る温度である10℃における燃料油中で析出する現象が起こる場合があることを確認した。 By the way, the present inventors have also studied the use of the fatty acid alkyl ester mixed with the light oil as described above. At that time, in the fatty acid alkyl ester mixed light oil composition, crystals derived from the fatty acid alkyl ester are sufficient in winter. It was confirmed that the phenomenon of precipitation in fuel oil at 10 ° C., which can be reached, may occur.
従来の軽油では、ワックス析出による低温流動性の評価として曇り点を使用しており、曇り点以上の温度ならば、長期貯蔵したとしてもワックス結晶が析出した例はなく、曇り点は結晶析出に関し信頼のおける値であった。しかしながら、前記の脂肪酸アルキルエステル混合軽油組成物においては、曇り点以上の温度であっても脂肪酸アルキルエステル由来の結晶析出が貯蔵時の燃料油中で恒常的に発生するのであれば、例えばSSタンクよりの燃料ラインにあるフィルターを閉塞させる恐れがあるほか、燃料油の低温性能に関しても、貯蔵した燃料を用いた場合には、軽油組成物の流動点や目詰まり点などの低温性能に関する試験結果より予想される実用性能を下回る可能性があることが容易に想像される。しかしながら、この現象に関する報告は未だなされておらず、そのため、この現象に係る問題を解決すべく検討を実施した例や、知見は存在していない。 Conventional gas oil uses a cloud point as an evaluation of low-temperature fluidity due to wax precipitation. If the temperature is higher than the cloud point, there is no example of wax crystals being precipitated even if stored for a long time, and the cloud point is related to crystal precipitation. It was a reliable value. However, in the fatty acid alkyl ester mixed light oil composition described above, if crystal precipitation derived from the fatty acid alkyl ester constantly occurs in the fuel oil during storage even at a temperature equal to or higher than the cloud point, for example, an SS tank In addition, there is a risk of clogging the filter in the fuel line, and the low-temperature performance of the fuel oil, when stored fuel is used, the test results on the low-temperature performance such as pour point and clogging point of the light oil composition It is easily imagined that there is a possibility that it may be less than the expected practical performance. However, no report has yet been made on this phenomenon, and therefore, there are no examples or knowledge that have been studied to solve the problem related to this phenomenon.
本発明の目的は、上記のような技術的な背景から、脂肪酸アルキルエステル燃料をディーゼルエンジン用燃料油に用いる軽油基材に混合して使用する際に問題となる、曇り点以上の温度での貯蔵における燃料油中への結晶析出、特に、ディーゼル車輌の燃料タンクと比較して、外気の影響による温度変化が小さい製油所のタンクやSSの地下タンクにおいても、冬季には十分達し得る温度である10℃での結晶析出を抑制したディーゼルエンジン用燃料油組成物を提供することを目的とする。 The object of the present invention is to solve the above-mentioned technical background, at a temperature higher than the cloud point, which is a problem when a fatty acid alkyl ester fuel is mixed with a light oil base material used for a diesel engine fuel oil. Crystallization in fuel oil during storage, especially in refinery tanks and SS underground tanks where the temperature change due to the influence of outside air is small compared to the fuel tanks of diesel vehicles It aims at providing the fuel oil composition for diesel engines which suppressed the crystal precipitation at a certain 10 degreeC.
本発明者らは、ディーゼルエンジン用燃料油組成物を様々な角度から分析し、鋭意検討を行った結果、曇り点以上の温度での貯蔵における燃料油中への結晶析出は、炭素数16、炭素数18以上の重質な飽和脂肪酸アルキルエステルと、それを生産する際に副生成物として発生するグリセリド類の相互作用に起因することをつきとめ、軽油基材と混合する炭素数16、炭素数18以上の重質な飽和脂肪酸アルキルエステル及びグリセリド類(ディーゼルエンジン用燃料油組成物に添加される潤滑性向上剤を代表とする各種添加剤も含む)の量を適切に調整し、更に、脂肪酸アルキルエステルを混合するベース軽油基材の性状を適切に調整することにより、出来上がりのディーゼルエンジン用燃料油組成物の溶解性を確保し、曇り点以上の温度での貯蔵における燃料油への結晶析出の抑制が可能であることを見出し、本発明に至った。すなわち、本発明は、以下に示す特徴を有するディーゼルエンジン用燃料油組成物を提供するものである。 As a result of analyzing the fuel oil composition for diesel engines from various angles and intensively examining the results, crystal precipitation in the fuel oil during storage at a temperature higher than the cloud point is 16 carbon atoms, We have determined that this is due to the interaction between heavy saturated fatty acid alkyl esters having 18 or more carbon atoms and glycerides generated as by-products when they are produced. The amount of 18 or more heavy saturated fatty acid alkyl esters and glycerides (including various additives typified by lubricity improvers added to diesel engine fuel oil compositions) are appropriately adjusted, and further fatty acids By appropriately adjusting the properties of the base gas oil base mixed with the alkyl ester, the solubility of the finished diesel engine fuel oil composition is ensured and the temperature above the cloud point. It found that it is possible to suppress the crystallization of the fuel oil in the reservoir, leading to the present invention. That is, the present invention provides a diesel engine fuel oil composition having the following characteristics.
(1)(a)10容量%留出温度が180〜235℃、90容量%留出温度が280〜350℃の蒸留性状を有し、硫黄分が10質量ppm以下であり、飽和分が80.6〜83.3容量%、芳香族分が16.7〜19.4容量%であり、アニリン点が45〜85℃で、かつ、カウリブタノール価が25.1〜26.7である軽油基材に、(b)モノ、ジ、トリグリセリドの合計含有量が0.85〜0.88質量%であり、その内ジグリセリド含有量が0〜0.3質量%、トリグリセリド含有量が0〜0.1質量%であり、かつ、カウリブタノール価が61.2〜63.6である脂肪酸アルキルエステルを0.1〜5.0質量%混合してなることを特徴とするディーゼルエンジン用燃料油組成物。
(2)前記脂肪酸アルキルエステルが、動植物油又は廃食油を含む油脂を原料として製造されたことを特徴とする上記(1)に記載のディーゼルエンジン用燃料油組成物。
(3)原油を常圧蒸留することにより得られた軽油留分を水素化脱硫する事により得られる上記(2)に記載のディーゼルエンジン用燃料油組成物。
(1) (a) It has a distillation property with a 10% by volume distillation temperature of 180 to 235 ° C., a 90% by volume distillation temperature of 280 to 350 ° C., a sulfur content of 10 mass ppm or less, and a saturated content of 80 A light oil having an aromatic content of 16.7 to 19.4 % by volume, an aniline point of 45 to 85 ° C., and a Kauri-butanol value of 25.1 to 26.7. The total content of (b) mono-, di-, and triglycerides is 0.85-0.88 mass% in the base material, of which the diglyceride content is 0-0.3 mass%, and the triglyceride content is 0-0. A fuel oil composition for diesel engines, comprising 0.1 to 5.0% by mass of a fatty acid alkyl ester having a Kauributanol number of 61.2 to 63.6 and a mass ratio of 0.1% by mass object.
(2) The fuel oil composition for a diesel engine according to (1), wherein the fatty acid alkyl ester is produced using a fat or oil containing animal or vegetable oil or waste cooking oil as a raw material.
(3) The fuel oil composition for a diesel engine according to (2), obtained by hydrodesulfurizing a light oil fraction obtained by subjecting crude oil to atmospheric distillation.
本発明のディーゼルエンジン用燃料油組成物は、脂肪酸アルキルエステルが混合されているにもかかわらず、曇り点以上の温度、特に10℃での貯蔵における燃料油中への結晶析出が抑制される。そして、流動点や、目詰まり点などの低温性能が優れている。 The fuel oil composition for a diesel engine of the present invention suppresses crystal precipitation in the fuel oil during storage at a temperature equal to or higher than the cloud point, particularly 10 ° C., even though the fatty acid alkyl ester is mixed. And low temperature performance, such as a pour point and a clogging point, is excellent.
以下、発明の詳細を記載する。
本発明におけるディーゼルエンジン用燃料油組成物に含有される脂肪酸アルキルエステルの量は、0.1〜5.0質量%、好ましくは0.5〜5質量%である。脂肪酸アルキルエステル含有量が5.0質量%以下であれば、脂肪酸アルキルエステルを燃料として使用した際に問題となる、酸化安定性、低温流動性への懸念がなく、かつ、含酸素燃料であることから、ディーゼル機関における燃焼状態を改善し、粒子状物質(PM)等を低減することができる。
Details of the invention will be described below.
The amount of the fatty acid alkyl ester contained in the diesel engine fuel oil composition in the present invention is 0.1 to 5.0 mass%, preferably 0.5 to 5 mass%. When the fatty acid alkyl ester content is 5.0% by mass or less, there is no concern about oxidation stability and low temperature fluidity, which is a problem when the fatty acid alkyl ester is used as a fuel, and it is an oxygen-containing fuel. Therefore, the combustion state in the diesel engine can be improved, and particulate matter (PM) and the like can be reduced.
本発明の脂肪酸アルキルエステルを混合したディーゼルエンジン用燃料油組成物における軽油基材の蒸留性状は、10容量%留出温度が180〜235℃、好ましくは183〜230℃、90容量%留出温度が280〜350℃、好ましくは315〜350℃である。
10容量%留出温度が180℃以上であれば、ディーゼルエンジン用燃料油組成物として適切な引火点、動粘度を保つことができ、235℃以下であれば、適度な揮発性を有することから、燃焼室内での空気との混合が促進され、不均一混合燃焼に由来する粒子状物質(PM)等を低減することができる。また、90容量%留出温度が280℃以上であれば、動粘度を適切に保つことができ、350℃以下であればディーゼルエンジン用燃料油組成物中の重質成分、特に芳香族分を低いレベルに抑えることができ、燃焼性を良好に保つことができる。
The distillation property of the light oil base in the diesel engine fuel oil composition mixed with the fatty acid alkyl ester of the present invention has a 10 vol% distillation temperature of 180 to 235 ° C, preferably 183 to 230 ° C, 90 vol% distillation temperature. Is 280 to 350 ° C, preferably 315 to 350 ° C.
If the 10% by volume distillation temperature is 180 ° C or higher, it can maintain an appropriate flash point and kinematic viscosity as a diesel engine fuel oil composition, and if it is 235 ° C or lower, it has moderate volatility. Mixing with air in the combustion chamber is promoted, and particulate matter (PM) and the like derived from heterogeneous mixed combustion can be reduced. Further, if the 90% by volume distillation temperature is 280 ° C or higher, the kinematic viscosity can be appropriately maintained, and if it is 350 ° C or lower, heavy components in the diesel engine fuel oil composition, particularly aromatic components, can be removed. It can be suppressed to a low level and good combustibility can be maintained.
また、本発明の脂肪酸アルキルエステルを混合したディーゼルエンジン用燃料油組成物における軽油基材に含まれる硫黄分は、10質量ppm以下、好ましくは8質量ppm以下である。
硫黄分を10質量ppm以下とすることで、エンジンから排出される粒子状物質(PM)の成分であるサルフェートの排出量が少なくなり、排ガス後処理装置の性能に対する影響も小さくなる。
なお、本発明における、蒸留性状はJIS K 2254の常圧法蒸留試験、硫黄分はJIS K 2541の微量電量滴定式酸化法により、それぞれ測定できる。
Moreover, the sulfur content contained in the light oil base material in the fuel oil composition for diesel engines mixed with the fatty acid alkyl ester of the present invention is 10 mass ppm or less, preferably 8 mass ppm or less.
By setting the sulfur content to 10 mass ppm or less, the amount of sulfate that is a component of particulate matter (PM) discharged from the engine is reduced, and the influence on the performance of the exhaust gas aftertreatment device is also reduced.
In the present invention, the distillation property can be measured by the atmospheric pressure distillation test of JIS K 2254, and the sulfur content can be measured by the microcoulometric titration method of JIS K 2541.
本発明の脂肪酸アルキルエステルを混合したディーゼルエンジン用燃料油組成物における軽油基材の飽和分は、70〜86容量%、好ましくは72〜85容量%、芳香族分は14〜30容量%、好ましくは15〜28容量%である。この芳香族分の内、2環芳香族類含有量は5.0容量%以下、好ましくは3.0容量%以下、3環以上の多環芳香族類の含有量は1.0容量%以下、好ましくは0.5容量%以下であることが好ましい。
芳香族分を14〜30容量%とすることにより、ディーゼルエンジン用燃料油組成物の溶解性を適切に保つことが可能となり、低温時に析出することで、フィルター閉塞の原因となるn−パラフィンの析出開始温度(曇り点)を低いレベルとすることができ、かつ、自動車の燃料系統に使用されるゴムパッキンの膨潤を適度に保つことを可能とし、燃料漏れなどのトラブルを回避できる。また、飽和分を70〜86容量%、芳香族分を14〜30容量%、特に2環、3環以上の多環芳香族を低レベルに抑えることにより、燃焼時にPM及びNOxの排出量を低減できる。
なお、ここでの組成割合は、JPI−5S−49−97「石油製品−炭化水素タイプ試験方法−高速液体クロマトグラフ法(HPLC)」に基づいて求められる。
In the fuel oil composition for diesel engines in which the fatty acid alkyl ester of the present invention is mixed, the saturated amount of the light oil base is 70 to 86% by volume, preferably 72 to 85% by volume, and the aromatic content is 14 to 30% by volume, preferably Is 15 to 28% by volume. Of this aromatic content, the content of bicyclic aromatics is 5.0% by volume or less, preferably 3.0% by volume or less, and the content of polycyclic aromatics having 3 or more rings is 1.0% by volume or less. Preferably, it is 0.5% by volume or less.
By adjusting the aromatic content to 14 to 30% by volume, it becomes possible to appropriately maintain the solubility of the fuel oil composition for diesel engines, and the precipitation of n-paraffin that causes filter blockage by precipitation at low temperatures. The deposition start temperature (cloud point) can be set to a low level, and the rubber packing used in the automobile fuel system can be appropriately swollen, and troubles such as fuel leakage can be avoided. In addition, the amount of PM and NOx emissions during combustion can be reduced by suppressing the saturated content to 70 to 86% by volume and the aromatic content to 14 to 30% by volume, especially polycyclic aromatics with 2 or 3 rings. Can be reduced.
In addition, the composition ratio here is calculated | required based on JPI-5S-49-97 "petroleum product-hydrocarbon type test method-high performance liquid chromatograph method (HPLC)".
本発明の脂肪酸アルキルエステルを混合したディーゼルエンジン用燃料油組成物における軽油基材のアニリン点は、45〜85℃、好ましくは45〜83℃である。
アニリン点が85℃以下であれば、ディーゼルエンジン用燃料油組成物の溶解力を適切に保つことが可能となる。また、各種ゴムを用いたシール材の観点からも、ゴム膨潤を適度にすることでシール性を確保することが可能となる。アニリン点が45℃以上であれば、軽油の成分中で、特にアニリン点を低くするに寄与の大きい芳香族分を上記のような適切な範囲に保つことが可能となるため、燃焼時のPM及びNOx排出量を低減することができる。
なお、ここでのアニリン点は、JIS K 2256「石油製品アニリン点及び混合アニリン点試験方法」に準拠して求められる。
The aniline point of the light oil base in the fuel oil composition for diesel engines mixed with the fatty acid alkyl ester of the present invention is 45 to 85 ° C, preferably 45 to 83 ° C.
If an aniline point is 85 degrees C or less, it will become possible to maintain the dissolving power of the fuel oil composition for diesel engines appropriately. Further, from the viewpoint of a sealing material using various rubbers, it is possible to ensure sealing performance by making rubber swelling moderate. If the aniline point is 45 ° C. or higher, it becomes possible to keep the aromatic component that contributes particularly to lowering the aniline point in the light oil component within the appropriate range as described above. In addition, NOx emissions can be reduced.
The aniline point here is determined according to JIS K 2256 “Petroleum product aniline point and mixed aniline point test method”.
本発明の脂肪酸アルキルエステルを混合したディーゼルエンジン用燃料油組成物における軽油基材のカウリブタノール価は、22〜50、好ましくは24〜50である。
カウリブタノール価が22以上であれば、ディーゼルエンジン用燃料油組成物に添加される種々の高分子量の添加剤を確実に溶解せしめ、製油所よりの出荷から、ユーザーの自動車に給油されるまでの各種フィルター、ならびに自動車の燃料系統にある各種フィルターをストレスなく通油させることができ、かつ、添加剤がフィルターでトラップされることもないため、調製初期と同等の品質を使用期間中維持することができる。また、曇り点以上の温度で長時間保管された際に生じる結晶の析出を抑制することができる。また、カウリブタノール価が50以下であれば、軽油基材の成分中で、特にカウリブタノール価上昇に寄与の大きいナフテン分、芳香族分を上記のような適切な範囲に保つことが可能となるため、燃焼時のPM及びNOx排出量を低減できる。
The kauri-butanol value of the light oil base in the fuel oil composition for diesel engines mixed with the fatty acid alkyl ester of the present invention is 22-50, preferably 24-50.
If the Kauributanol number is 22 or more, various high molecular weight additives added to the fuel oil composition for diesel engines are surely dissolved, and from shipment from the refinery to refueling to the user's automobile. Various filters and various filters in the fuel system of automobiles can be passed through without stress, and since additives are not trapped by the filters, the quality equivalent to the initial stage of preparation should be maintained during the period of use. Can do. In addition, it is possible to suppress the precipitation of crystals that occur when stored for a long time at a temperature equal to or higher than the cloud point. Further, if the Kauri-butanol value is 50 or less, it becomes possible to keep the naphthene content and aromatic content that contribute particularly to the increase in Kauri-butanol value in the components of the light oil base in the appropriate ranges as described above. Therefore, PM and NOx emission during combustion can be reduced.
ここでのカウリブタノール価は、炭化水素の相対的溶解力を示すもので、カウリブタノール価が高いほど、樹脂溶解性が高いことを示す。本発明におけるカウリブタノール価の測定法は、ASTM D 1133に準拠し、下記の方法により求めることができる。
すなわち、天然カウリ樹脂とブチルアルコールで調製した標準カウリブタノール溶液20±0.1gを200ミリリットル(以下、「mL」と記す)の三角フラスコにとり、この三角フラスコを25±1℃に保った水溶液に浸す。次に、先ずトルエンをビュレットに採り、上記の三角フラスコ内に滴定する。終点は、フラスコの下に印刷活字を置き、活字の字画が不鮮明になったときとする。同様に、トルエンとn−ヘプタンとの混合液(容量割合でトルエン25:n−ヘプタン75)についても滴定する。そして、カウリブタノール価測定対象油(以下、「試料」と言う)をビュレットにとり、同様の操作で滴定する。カウリブタノール価は、下記数1の式によって算出する。
《数1》
カウリブタノール価={〔65(C−B)〕/〔A−B〕} + 40
A:滴定に要したトルエンの量(mL)
B:滴定に要したn−ヘプタン・トルエン混合液の量(mL)
C:滴定に供した試料の量(mL)
なお、上記のカウリブタノール価の測定法において、標準カウリブタノール溶液は、トルエンで滴定したときカウリブタノール価が100〜110で、容量割合でトルエン25:ヘプタン75の混合液で滴定したときカウリブタノール価が40になるように予め調整しておく。
The Kauri-butanol value here indicates the relative dissolving power of hydrocarbons, and the higher the Kauri-butanol value, the higher the resin solubility. The method for measuring the Kauri-butanol value in the present invention can be determined by the following method based on ASTM D 1133.
That is, 20 ± 0.1 g of a standard kauributanol solution prepared with natural kauri resin and butyl alcohol was placed in a 200 milliliter (hereinafter referred to as “mL”) Erlenmeyer flask, and the Erlenmeyer flask was added to an aqueous solution maintained at 25 ± 1 ° C. Immerse. Next, toluene is first taken into a burette and titrated into the above Erlenmeyer flask. The end point is when a printed type is placed under the flask and the type stroke becomes unclear. Similarly, titration is also performed for a mixed solution of toluene and n-heptane (volume ratio of toluene 25: n-heptane 75). Then, oil for measuring the Kauri-butanol value (hereinafter referred to as “sample”) is taken in a burette and titrated by the same operation. The Kauri-butanol value is calculated by the following equation (1).
<< Equation 1 >>
Kauri-butanol value = {[65 (CB)] / [AB]} + 40
A: Amount of toluene required for titration (mL)
B: Amount of n-heptane / toluene mixed solution required for titration (mL)
C: Amount of sample subjected to titration (mL)
In the above Kauri-butanol number measurement method, the standard Kauri-butanol solution has a Kauri-butanol value of 100 to 110 when titrated with toluene, and a Kauri-butanol value when titrated with a mixed solution of toluene 25: heptane 75 at a volume ratio. Is adjusted in advance to be 40.
本発明におけるディーゼルエンジン用燃料油組成物に混合する脂肪酸アルキルエステルは、モノ、ジ、トリグリセリドの合計含有量が0.01〜1.0質量%であり、好ましくは0.01〜0.95質量%であり、その内、ジグリセリドが0〜0.3質量%、好ましくは0〜0.2質量%であり、トリグリセリドが0〜0.1質量%、好ましくは0〜0.05質量%である。なお、ジグリセリドおよびトリグリセリドは任意成分である。また、カウリブタノール価が50〜65、好ましくは55〜65である。
上記のカウリブタノール価の範囲にある脂肪酸アルキルエステルを生産する際に副生成物として発生するグリセリド類は、融点が高く、ミリスチン酸アルキルエステル、及びパルミチン酸アルキルエステル以上の重質な飽和脂肪酸アルキルエステルとの相互作用により、曇り点以上での貯蔵において結晶を析出させる恐れがあるため、本発明で用いる脂肪酸アルキルエステルのグリセリド類の含有量は上記の範囲内である。
なお、ここでのグリセリド量は、EN14105「Fat and oil derivatives - Fatty Acid Methyl Ester(FAME) - Determination of free and total glycerol and mono−, di−、 triglyceride contents」に準拠し測定した。
The fatty acid alkyl ester to be mixed with the diesel engine fuel oil composition in the present invention has a total content of mono-, di-, and triglycerides of 0.01 to 1.0 mass%, preferably 0.01 to 0.95 mass. Among them, diglyceride is 0 to 0.3% by mass, preferably 0 to 0.2% by mass, and triglyceride is 0 to 0.1% by mass, preferably 0 to 0.05% by mass. . Diglyceride and triglyceride are optional components. The Kauri-butanol value is 50 to 65, preferably 55 to 65.
The glycerides generated as a by-product when producing fatty acid alkyl esters in the above-mentioned range of kauributanol values have a high melting point and are heavy saturated fatty acid alkyl esters higher than myristic acid alkyl esters and palmitic acid alkyl esters. The content of the glycerides of the fatty acid alkyl ester used in the present invention is within the above-mentioned range because there is a risk that crystals may precipitate due to the interaction with the above-mentioned in storage above the cloud point.
In addition, the amount of glycerides here is measured according to EN14105 “Fat and oil derivatives-Fatty Acid Methyl Ester (FAME)-Determination of free and total glycerol and mono-, tri-cylinder”.
本発明におけるディーゼルエンジン用燃料油組成物に混合する脂肪酸アルキルエステルのカウリブタノール価は上記のように50〜65であるが、カウリブタノール価が50以上であれば、軽油基材と混合した際に発生する溶解度の低下に伴うスラッジの発生や、添加剤等の溶解性低下による通油性の低下を抑制することができ、65以下であれば、脂肪酸アルキルエステル中の組成がミリスチン酸アルキルエステル、及びパルミチン酸アルキルエステル(両アルキルエステルの構造については、後記の脂肪酸アルキルエステル代表例の表1を参照)などの比較的重質な飽和脂肪酸アルキルエステルが豊富なことを示しており、つまりは脂肪酸アルキルエステル自体の酸化安定性が良好であることから、軽油基材との混合量を適切にすることで、軽油と遜色ない酸化安定性を維持することができる。
なお、ここでのカウリブタノール価は、前記の通りのASTM D 1133に基づいて求められる。
The Kauri-butanol value of the fatty acid alkyl ester mixed with the fuel oil composition for diesel engines in the present invention is 50 to 65 as described above, but when the Kauri-butanol value is 50 or more, it is mixed with the light oil base material. It is possible to suppress the generation of sludge due to the decrease in solubility generated and the decrease in oil permeability due to the decrease in solubility of additives and the like, and if it is 65 or less, the composition in the fatty acid alkyl ester is myristic acid alkyl ester, and This indicates that a relatively heavy saturated fatty acid alkyl ester such as palmitic acid alkyl ester (for the structure of both alkyl esters, see Table 1 in the fatty acid alkyl ester representative examples below) is abundant. Since the oxidation stability of the ester itself is good, the mixing amount with the light oil base material should be appropriate. , It is possible to maintain the diesel fuel and not inferior oxidation stability.
Here, the Kauri-butanol value is determined based on ASTM D 1133 as described above.
本発明におけるディーゼルエンジン用燃料油組成物に混合されている脂肪酸アルキルエステルは、動植物油、又は廃食油などの油脂を原料としていることが好ましい。
動植物油、又は廃食油などの油脂を原料とした脂肪酸アルキルエステルは、硫黄分を含まないため、軽油基材に混合することにより、ディーゼルエンジン用燃料油組成物中の硫黄分をより低レベルに抑えることが可能となり、エンジンから排出される粒子状物質(PM)の成分であるサルフェートの排出量を少なくし、排ガス後処理装置の性能に対する影響も小さくなり好ましい。また、パーム油、ナタネ油、大豆油、ココナツ油等の植物油系油脂の利用は、再生可能エネルギーと位置付けられていることから、国際間の二酸化炭素削減プロコトル(京都議定書)においてはカーボンニュートラルな燃料であるとされ、二酸化炭素排出量削減の観点からも好ましく、その中でも、ヤトロファに代表される非食料系の植物油の使用は、食料と燃料の競合による食料問題の観点や、荒地などでの栽培も可能なことから、荒地の緑地化という観点において、より好ましい。
原料油脂からの脂肪酸アルキルエステル製造のための反応方法及び精製については、一般的なアルカリ金属を用いたアルカリ触媒法、有機酸などの酸触媒を用いた酸触媒法、リパーゼ酵素を用いたリパーゼ法などがあるが、本発明において用いられる脂肪酸アルキルエステルは、反応・精製法を問わない。
本発明で使用される脂肪酸アルキルエステルのアルキル基は、例えばメチル基、エチル基、プロピル基、ブチル基、ペンチル基、およびヘキシル基などの、異性体を含む各種アルキル基である。下記表1に、上記アルキル基が結合した脂肪酸アルキルエステルの代表例を示す。ただし、本発明において、使用される脂肪酸アルキルエステルの種類は、下記代表例に限定されるものではない。
The fatty acid alkyl ester mixed in the diesel engine fuel oil composition in the present invention is preferably made from fats and oils such as animal and vegetable oils or waste cooking oil.
Fatty acid alkyl esters made from animal and vegetable oils or oils and fats such as waste edible oils do not contain sulfur, so mixing them with diesel oil bases will lower the sulfur content in diesel engine fuel oil compositions. It is possible to reduce the amount of sulfate, which is a component of particulate matter (PM) discharged from the engine, and the effect on the performance of the exhaust gas aftertreatment device is also reduced. In addition, the use of vegetable oils such as palm oil, rapeseed oil, soybean oil, and coconut oil is regarded as a renewable energy. Therefore, carbon neutral fuel is used in the international CO2 reduction protocol (Kyoto Protocol). This is also preferable from the viewpoint of reducing carbon dioxide emissions. Among them, the use of non-food-based vegetable oils, represented by Jatropha, can be used in terms of food problems due to competition between food and fuel, and cultivation in wasteland. From the viewpoint of greening of wasteland, it is more preferable.
Regarding the reaction method and purification for fatty acid alkyl ester production from raw oil and fat, general alkali catalyst method using alkali metal, acid catalyst method using acid catalyst such as organic acid, lipase method using lipase enzyme The fatty acid alkyl ester used in the present invention is not limited to the reaction / purification method.
The alkyl group of the fatty acid alkyl ester used in the present invention is various alkyl groups including isomers such as methyl group, ethyl group, propyl group, butyl group, pentyl group, and hexyl group. Table 1 below shows representative examples of fatty acid alkyl esters to which the alkyl group is bonded. However, in the present invention, the type of fatty acid alkyl ester used is not limited to the following representative examples.
本発明で使用される脂肪酸アルキルエステル及び原料に使用される油脂の脂肪酸の分析は、ガスクロマトグラフ(GC)を用いて行うことが可能である。 Analysis of fatty acid alkyl esters used in the present invention and fatty acids in fats and oils used as raw materials can be performed using a gas chromatograph (GC).
本発明のディーゼルエンジン用燃料油組成物においては、潤滑性向上剤は添加しない方が好ましいが、必要に応じて添加することができる。その場合の含有量は、10〜50質量ppmが好ましい。 In the fuel oil composition for a diesel engine of the present invention, it is preferable not to add a lubricity improver, but it can be added as necessary. The content in that case is preferably 10 to 50 mass ppm.
本発明は、炭素数16、炭素数18以上の重質な飽和脂肪酸アルキルエステルと、それを生産する際に副生成物として発生するグリセリド類の相互作用により発生する結晶析出を抑制したディーゼルエンジン用燃料油組成物であって、曇り点以上の温度、特に10℃での貯蔵における燃料油中への結晶析出を抑制するためには、得られるディーゼルエンジン用燃料油組成物に含有される上記の脂肪酸アルキルエステルとグリセリド類の量を調整する必要がある。一方、潤滑性向上剤の主成分もまた脂肪酸、又は脂肪酸アルキルエステル、もしくはグリセリド類であることから、本発明の燃料油組成物の場合、上記の理由により、潤滑性向上剤の影響も鑑みる必要がある。よって、本発明のディーゼルエンジン用燃料油組成物に潤滑性向上剤を添加する場合は10〜50質量ppmが好ましい。潤滑性向上剤の添加量を上記の範囲とすることにより、曇り点以上の温度、特に10℃での常温長期貯蔵時に燃料油中への結晶の析出を抑制することができ、本発明の燃料油組成物のフィルタビリティーを良好に維持することができる。 The present invention is for a diesel engine that suppresses the precipitation of crystals caused by the interaction of a heavy saturated fatty acid alkyl ester having 16 or more carbon atoms and 18 or more carbon atoms and glycerides that are generated as by-products when producing the same. In order to suppress crystallization of the fuel oil composition in the fuel oil during storage at a temperature above the cloud point, particularly at 10 ° C., the fuel oil composition for diesel engines obtained above is contained. It is necessary to adjust the amount of fatty acid alkyl ester and glycerides. On the other hand, since the main component of the lubricity improver is also a fatty acid, a fatty acid alkyl ester, or glycerides, in the case of the fuel oil composition of the present invention, it is necessary to consider the influence of the lubricity improver for the above reasons. There is. Therefore, 10-50 mass ppm is preferable when adding a lubricity improver to the fuel oil composition for diesel engines of the present invention. By making the addition amount of the lubricity improver within the above range, it is possible to suppress the precipitation of crystals in the fuel oil during normal temperature long-term storage at a temperature above the cloud point, particularly at 10 ° C., and the fuel of the present invention The filterability of the oil composition can be maintained well.
本発明におけるディーゼルエンジン用燃料油組成物の15℃における密度は、0.70〜0.86g/cm3、好ましくは0.75〜0.86g/cm3であることが好ましい。15℃における密度が0.70〜0.86g/cm3であれば、軽油の使用を前提に設計されたディーゼル車に対し、ディーゼル燃焼時の着火性を維持し、適切な燃焼状態を保つことができるため好ましい。
なお、15℃における密度はJIS K 2249の密度試験方法及び密度・質量・容量換算表により測定することができる。
The density at 15 ° C. of the diesel engine fuel oil composition in the present invention is preferably 0.70 to 0.86 g / cm 3 , preferably 0.75 to 0.86 g / cm 3 . If the density at 15 ° C. is 0.70 to 0.86 g / cm 3 , maintain ignitability during diesel combustion and maintain an appropriate combustion state for diesel vehicles designed on the premise of using diesel oil. Is preferable.
The density at 15 ° C. can be measured by a density test method of JIS K 2249 and a density / mass / capacity conversion table.
本発明におけるディーゼルエンジン用燃料油組成物の30℃動粘度は、1.700〜6.000mm2/s、好ましくは2.000〜5.800mm2/sであることが好ましい。30℃における動粘度が1.700〜6.000mm2/sであれば、軽油の使用を前提に設計されたディーゼル車に対し、燃料供給ポンプの磨耗や、燃料自体の流動性の面で適切に使用することが可能であるため好ましい。
なお、30℃における動粘度はJIS K 2283の動粘度試験方法及び粘度指数算出方法により測定することができる。
The 30 ° C. kinematic viscosity of the diesel engine fuel oil composition in the present invention is preferably 1.700 to 6.000 mm 2 / s, more preferably 2.00 to 5.800 mm 2 / s. If the kinematic viscosity at 30 ° C is 1.700 to 6.000 mm 2 / s, it is suitable for diesel vehicles designed on the basis of the use of light oil in terms of wear of the fuel supply pump and fluidity of the fuel itself It is preferable because it can be used for
The kinematic viscosity at 30 ° C. can be measured by a kinematic viscosity test method and a viscosity index calculation method of JIS K 2283.
本発明におけるディーゼルエンジン用燃料油組成物の引火点は、45〜100℃、好ましくは45〜95℃であることが好ましい。この範囲内ならば、火気による引火の危険性が低く、一般車はもちろんのこと、特にディーゼルエンジンの使用率が高く、かつ使用現場での給油の機会が多い重機等を取り扱う際にも好ましい。
なお、引火点は、JIS K 2265−3の引火点の求め方−第3部:ペンスキーマルテンス密閉法により測定することができる。
The flash point of the diesel engine fuel oil composition in the present invention is 45 to 100 ° C, preferably 45 to 95 ° C. Within this range, the risk of ignition by fire is low, and it is preferable not only for handling ordinary vehicles but also for heavy machinery that has a high usage rate of diesel engines and has many opportunities for refueling at the site of use.
The flash point can be measured by the method of obtaining the flash point of JIS K 2265-3-Part 3: Penschem Lutens sealing method.
本発明のディーゼルエンジン用燃料油組成物に用いる軽油基材は、種々の石油留分から、蒸留によりその蒸留性状を調整し、水素化脱硫、芳香族抽出処理等の処理によりその組成を調整し、上記本発明に規定する性状を満たすようにして製造することができる。本発明の燃料油組成物は、JIS規格に定められている軽油の、特1号、1号、2号、3号、特3号のいずれにも適用可能である。本発明の燃料油組成物に用いる軽油基材の製造方法は、上記本発明に規定する性状を満たす限りにおいて特に制限されない。例えば、原油の常圧蒸留で得られた軽油留分や、灯油留分と軽油留分の混合物や、重油を接触分解、水素化脱硫、水素化分解処理、脱アロマ処理及びコーカー等で重質油分をアップグレーディング等した後に分留される軽油留分など種々の留分を用いて製造することができる。そして、本発明のディーゼルエンジン用燃料油組成物は、上記のようにして得られる本発明に規定する性状を満たす軽油基材に、上記のような本発明に規定する性状を満たす脂肪酸アルキルエステルを、上記のような比率で混合して製造することができる。 The light oil base material used for the diesel engine fuel oil composition of the present invention adjusts its distillation properties by distillation from various petroleum fractions, and adjusts its composition by treatment such as hydrodesulfurization and aromatic extraction treatment, It can be manufactured so as to satisfy the properties defined in the present invention. The fuel oil composition of the present invention can be applied to any of No. 1, No. 1, No. 2, No. 3, and No. 3 of diesel oil defined in JIS standards. The manufacturing method of the light oil base material used for the fuel oil composition of the present invention is not particularly limited as long as the properties defined in the present invention are satisfied. For example, gas oil fraction obtained by atmospheric distillation of crude oil, a mixture of kerosene fraction and light oil fraction, heavy oil is catalytically cracked, hydrodesulfurized, hydrocracked, dearomatized and coker heavy. It can be produced using various fractions such as a light oil fraction that is fractionated after the oil is upgraded or the like. And the fuel oil composition for diesel engines of this invention is a fatty-acid alkylester which satisfy | fills the property prescribed | regulated to the above invention to the light oil base material which satisfy | fills the property prescribed | regulated to this invention obtained as mentioned above. , And can be produced by mixing at the ratio as described above.
本発明のディーゼルエンジン用燃料油組成物には、低温流動性向上剤を10〜1000容量ppm、好ましくは50〜700容量ppm添加することが好ましい。低温流動性向上剤を10容量ppm以上添加することにより、目詰まり点(CFPP)や流動点(PP)を改善することができ好ましい。また低温流動性向上剤の添加量が1000容量ppm以下であることにより、添加剤自体の凝集等を防ぐことができ好ましい。 It is preferable to add the low temperature fluidity improver to the fuel oil composition for a diesel engine of the present invention in an amount of 10 to 1000 ppm by volume, preferably 50 to 700 ppm by volume. Addition of 10 ppm by volume or more of the low temperature fluidity improver is preferable because the clogging point (CFPP) and the pour point (PP) can be improved. Moreover, it is preferable that the addition amount of the low temperature fluidity improver is 1000 ppm by volume or less because aggregation of the additive itself can be prevented.
本発明において使用する低温流動性向上剤は、種々のものが使用でき、その例として、アルケニルコハク酸イミド、エチレン−酢酸ビニル共重合体、エチレン−アルキルアクリレート共重合体、ポリエチレングリコール誘導体等の共重合ポリマー、塩素化ポリエチレン、ポリアルキルアクリレート等のポリマーが挙げられる。これらの低温流動性向上剤は、1種単独で用いても良いし、2種以上を組合せて用いても良い。 Various low-temperature fluidity improvers used in the present invention can be used. Examples thereof include alkenyl succinimide, ethylene-vinyl acetate copolymer, ethylene-alkyl acrylate copolymer, polyethylene glycol derivative and the like. Polymers such as polymerized polymers, chlorinated polyethylene, and polyalkyl acrylates may be mentioned. These low temperature fluidity improvers may be used alone or in combination of two or more.
また、本発明のディーゼルエンジン用燃料油組成物には、必要に応じて、その他各種の添加剤を適宜配合することができる。このような添加剤としては、例えばセタン価向上剤、界面活性剤、防腐剤、防錆剤、泡消剤、清浄剤、酸化防止剤、および色相改善剤など公知の燃料添加剤が挙げられる。これらを一種又は数種組合せて添加することができる。 Moreover, various other additives can be suitably mix | blended with the fuel oil composition for diesel engines of this invention as needed. Examples of such additives include known fuel additives such as a cetane number improver, a surfactant, an antiseptic, a rust inhibitor, a defoamer, a detergent, an antioxidant, and a hue improver. These can be added singly or in combination.
次に、本発明を実施例、比較例により更に具体的に説明する。なお本発明は、これらの例によって何ら制限されるものではない。 Next, the present invention will be described more specifically with reference to examples and comparative examples. In addition, this invention is not restrict | limited at all by these examples.
実施例、比較例において、引火点、蒸留性状、硫黄分、30℃動粘度は、JIS K 2204に定められる方法に準拠して測定を行った。その他に、15℃密度は、JIS K 2249、曇り点は、JIS K 2269、アニリン点は、JIS K 2256により測定を行った。 In Examples and Comparative Examples, the flash point, distillation properties, sulfur content, and 30 ° C. kinematic viscosity were measured according to the method defined in JIS K 2204. In addition, the 15 ° C. density was measured according to JIS K 2249, the cloud point was measured according to JIS K 2269, and the aniline point was measured according to JIS K 2256.
飽和分、芳香族分の割合と、芳香族分の環数別割合は、JPI-5S-49-97に基づいて測定を行った。HPLCの装置構成及び分析条件を以下に示す。
装置:Agilent 1100 Series(ALS:g1329A, Bin Pump: G1312A, Degasser: G1379A, Rid: G1362A, Colcom: G1316A)
移動相:n−ヘキサン
流量:1.0ml/min
カラム:硝酸銀含浸シリカカラム(4.6mml.D.*70mmL. センシュー科学製AgNO3−1071−Y)
アミン修飾カラム(4.0mml.D.*250mmL. 2本 センシュー科学製 LICHROSORB−NH2)
カラム温度:35℃
試料濃度:10vol%
注入量:5μl
The ratio of the saturated component, the aromatic component, and the aromatic component according to the number of rings were measured based on JPI-5S-49-97. The apparatus configuration and analysis conditions of HPLC are shown below.
Equipment: Agilent 1100 Series (ALS: g1329A, Bin Pump: G1312A, Degasser: G1379A, Rid: G1362A, Colcom: G1316A)
Mobile phase: n-hexane Flow rate: 1.0 ml / min
Column: Silver nitrate impregnated silica column (4.6 ml. D. * 70 mmL. AgNO 3 -1071-Y manufactured by Senshu Scientific)
Amine-modified column (4.0mml.D. * 250mmL. 2 present Senshu Scientific Co. LICHROSORB-NH 2)
Column temperature: 35 ° C
Sample concentration: 10 vol%
Injection volume: 5 μl
パラフィン類の含有量およびナフテン類の含有量は下記方法により求めた。
まず試料をHPLCにより飽和分と芳香族分とに分画後、飽和分についてGC−MSによりタイプ分析を行った。ここで得られた分析結果を基に、ASTM D 2786に従って解析を行い、飽和分中のパラフィン類と、ナフテン類の含有割合を求めた。また、ここで得られた飽和分中の環数別ナフテン類の割合を、上記のように求めた飽和分割合に乗ずることで、ナフテン類の含有量を求めた。
分析条件を下記に示す。
装置:HP−6890 HP5973 四重極質量分析計
カラム:DB−1:30m×0.25mmI.D.×0.25μm
オーブン温度:40℃(1min)→10℃/min→280℃(5min)
注入口温度:43℃ Oven track mode ON
インターフェース温度:300℃
キャリアガス:He:55KPa Constant flow mode ON
Solvent Delay:4.5min
質量範囲:50〜500 Threshold=100 Sampling♯3
イオン化電圧:70eV
注入方法:オンカラム注入 1.0μl
The content of paraffins and the content of naphthenes were determined by the following methods.
First, the sample was fractionated into a saturated component and an aromatic component by HPLC, and then type analysis was performed on the saturated component by GC-MS. Based on the analysis result obtained here, analysis was performed according to ASTM D 2786, and the content ratio of paraffins and naphthenes in the saturated content was determined. Moreover, the content of naphthenes was determined by multiplying the ratio of naphthenes by number of rings in the saturation obtained here by the saturation ratio determined as described above.
The analysis conditions are shown below.
Apparatus: HP-6890 HP5973 Quadrupole mass spectrometer Column: DB-1: 30 m × 0.25 mm I.D. D. × 0.25μm
Oven temperature: 40 ° C. (1 min) → 10 ° C./min→280° C. (5 min)
Inlet temperature: 43 ° C. Even track mode ON
Interface temperature: 300 ° C
Carrier gas: He: 55 KPa Constant flow mode ON
Solvent Delay: 4.5min
Mass range: 50-500 Threshold = 100 Sampling # 3
Ionization voltage: 70 eV
Injection method: On-column injection 1.0 μl
n−パラフィン含有量は、ガスクロマトグラフィ(GC)により測定を行った。以下に測定条件を示す。
・軽油基材とディーゼルエンジン用燃料油組成物について
装置:5890 series2(Agilent Technologies)
カラム:Ultra 1 (Agilent) Crosslinked Methyl Silicone Gum,50m×0.20mmI.D.
膜厚0.33μm
検出器:FID
オーブン温度:60℃(0min)−(6℃/min)→ 340℃(10min) Run 56.7min
注入口:On−column
注入口温度:オーブントラックモード(オーブン温度+3℃)
検出器温度:350℃
キャリアガス:He 280kPa (定圧) 1.3ml/min 線速度29.7cm/sec(at 60℃)
メイクアップガス:He
FID燃焼ガス:H2 30 ml/min , Air 400ml/min
注入量:0.2μl
定量法:内標準法(内標準物質:フタル酸ジブチルエステル)
The n-paraffin content was measured by gas chromatography (GC). The measurement conditions are shown below.
-About light oil base material and fuel oil composition for diesel engine Equipment: 5890 series2 (Agilent Technologies)
Column: Ultra 1 (Agilent) Crosslinked Methyl Silicone Gum, 50 m × 0.20 mm I.D. D.
Film thickness 0.33μm
Detector: FID
Oven temperature: 60 ° C. (0 min) − (6 ° C./min)→340° C. (10 min) Run 56.7 min
Inlet: On-column
Inlet temperature: oven track mode (oven temperature + 3 ° C)
Detector temperature: 350 ° C
Carrier gas: He 280 kPa (constant pressure) 1.3 ml / min Linear velocity 29.7 cm / sec (at 60 ° C.)
Make-up gas: He
FID combustion gas: H 2 30 ml / min, Air 400 ml / min
Injection volume: 0.2 μl
Quantitative method: Internal standard method (Internal standard substance: Dibutyl phthalate)
〔ディーゼルエンジン用燃料油組成物の調製〕
(実施例1、2、比較例1〜4)
表2に示した性状の軽油基材、及び表3に示した性状の脂肪酸アルキルエステルを用い、これらの軽油基材と脂肪酸アルキルエステルを表4に示した配合比で混合し、ディーゼルエンジン用燃料油組成物を調製した。得られた燃料油組成物の性状を表4に示した。なお、潤滑性向上剤としては主成分が脂肪酸、脂肪酸アルキルエステル、またはグリセリド類である潤滑性向上剤を用いた。
[Preparation of Diesel Engine Fuel Oil Composition]
(Examples 1 and 2 and Comparative Examples 1 to 4)
Using diesel oil bases having the properties shown in Table 2 and fatty acid alkyl esters having the properties shown in Table 3, these diesel oil bases and fatty acid alkyl esters are mixed at the blending ratios shown in Table 4, and fuel for diesel engines An oil composition was prepared. Properties of the obtained fuel oil composition are shown in Table 4. As the lubricity improver, a lubricity improver whose main component is a fatty acid, a fatty acid alkyl ester, or glycerides was used.
〔貯蔵時の結晶析出試験〕
実施例、比較例で得られた燃料油組成物を用いて、貯蔵時の結晶析出試験を行った。この試験は下記の手順により実施した。
試験燃料100mLをスクリュー瓶に採取し、50℃にて1時間加熱した。1時間経過後、サンプルを室温にて30分放冷した。放冷した後、10℃に保たれた恒温槽に静置し、12時間毎に結晶の析出を目視にて確認した。そして、10℃における貯蔵において、1ヶ月経過後の液中に結晶の析出が確認されなければ「○」と、結晶の析出が確認されれば「×」と判定した。
上記結晶析出試験の判定結果を表4に示した。
なお、本試験は脂肪酸アルキルエステルに由来する結晶析出を1ヶ月貯蔵したもので確認するものであり、曇り点の測定は実施例、比較例で得られた燃料油組成物を調合後、JIS K 2269に準拠し測定したものである。
[Crystal precipitation test during storage]
Using the fuel oil compositions obtained in Examples and Comparative Examples, a crystal precipitation test during storage was performed. This test was performed according to the following procedure.
100 mL of the test fuel was collected in a screw bottle and heated at 50 ° C. for 1 hour. After 1 hour, the sample was allowed to cool at room temperature for 30 minutes. After standing to cool, it was left still in a thermostat kept at 10 ° C., and crystal precipitation was visually confirmed every 12 hours. Then, in storage at 10 ° C., it was determined as “◯” if no crystal precipitation was confirmed in the liquid after one month, and “x” if crystal precipitation was confirmed.
Table 4 shows the determination results of the crystal precipitation test.
In addition, this test confirms that the crystal precipitation derived from the fatty acid alkyl ester is stored for 1 month, and the cloud point is measured after preparing the fuel oil compositions obtained in Examples and Comparative Examples, and then JIS K. It was measured according to 2269.
上記結晶析出試験における10℃で1ヶ月貯蔵後の、実施例1で得られた燃料油組成物を図1として、比較例1〜4で得られた燃料油組成物を図2として、比較例1で得られた燃料油組成物の結晶を図3としてそれぞれ示した。 The fuel oil composition obtained in Example 1 after storage for 1 month at 10 ° C. in the above crystal precipitation test is shown in FIG. 1 and the fuel oil compositions obtained in Comparative Examples 1 to 4 are shown in FIG. The crystals of the fuel oil composition obtained in 1 are shown in FIG.
表4に示したように、実施例1、2で得られた燃料油組成物においては、10℃における1ヶ月間の貯蔵試験において、結晶の析出は確認されず、混合する軽油基材、脂肪酸アルキルエステルの適切な調製により、結晶析出が抑制されていることがわかった。
一方、比較例1で得られた燃料油組成物においては、潤滑性向上剤が多いため、脂肪酸アルキルエステルとの相互作用により、結晶の析出が確認された。また、比較例2で得られた燃料油組成物においては、脂肪酸アルキルエステル混合量が10質量%と多すぎることから、結晶の析出が確認された。比較例3で得られた燃料油組成物においては、ベースとなる軽油基材の性状、特にカウリブタノール価やアニリン点などの、燃料油の溶解性を示すパラメーターが低いため、結晶の析出を抑制できていない。そして、比較例4で得られた燃料油組成物においては、軽油基材へ混合する脂肪酸アルキルエステルのグリセリド量が非常に多く、軽油基材で薄めたとしても曇り点以上での結晶の析出を助長しているのが確認された。
As shown in Table 4, in the fuel oil compositions obtained in Examples 1 and 2, in the storage test for 1 month at 10 ° C., no precipitation of crystals was confirmed, and the light oil base material and fatty acid to be mixed It was found that crystal precipitation was suppressed by appropriate preparation of the alkyl ester.
On the other hand, in the fuel oil composition obtained in Comparative Example 1, since there were many lubricity improvers, precipitation of crystals was confirmed by interaction with the fatty acid alkyl ester. Moreover, in the fuel oil composition obtained in Comparative Example 2, the amount of fatty acid alkyl ester mixed was as large as 10% by mass, so that precipitation of crystals was confirmed. In the fuel oil composition obtained in Comparative Example 3, the properties of the base gas oil base, particularly the parameters indicating the solubility of the fuel oil, such as the kauri-butanol number and the aniline point, are low, so that the precipitation of crystals is suppressed. Not done. And in the fuel oil composition obtained in Comparative Example 4, the amount of glycerides of the fatty acid alkyl ester mixed with the light oil base material is very large, and even if it is diluted with the light oil base material, the crystals are precipitated at the cloud point or higher. It was confirmed that it was promoting.
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