JP5153147B2 - Gasoline composition - Google Patents
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- JP5153147B2 JP5153147B2 JP2007011523A JP2007011523A JP5153147B2 JP 5153147 B2 JP5153147 B2 JP 5153147B2 JP 2007011523 A JP2007011523 A JP 2007011523A JP 2007011523 A JP2007011523 A JP 2007011523A JP 5153147 B2 JP5153147 B2 JP 5153147B2
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- 239000003502 gasoline Substances 0.000 title claims description 50
- 239000000203 mixture Substances 0.000 title claims description 25
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 24
- 238000004821 distillation Methods 0.000 claims description 15
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims description 15
- FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical compound CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 claims description 14
- LAAVYEUJEMRIGF-UHFFFAOYSA-N 2,4,4-trimethylpent-2-ene Chemical compound CC(C)=CC(C)(C)C LAAVYEUJEMRIGF-UHFFFAOYSA-N 0.000 claims description 14
- 125000003118 aryl group Chemical group 0.000 claims description 9
- 150000001336 alkenes Chemical class 0.000 claims description 7
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 239000011593 sulfur Substances 0.000 claims description 5
- 239000002994 raw material Substances 0.000 claims description 3
- 235000014676 Phragmites communis Nutrition 0.000 claims description 2
- 238000000034 method Methods 0.000 description 26
- 239000002585 base Substances 0.000 description 13
- 239000000463 material Substances 0.000 description 11
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- 239000007789 gas Substances 0.000 description 9
- 230000007613 environmental effect Effects 0.000 description 8
- 230000003749 cleanliness Effects 0.000 description 7
- 239000003208 petroleum Substances 0.000 description 6
- 238000001833 catalytic reforming Methods 0.000 description 5
- 230000007423 decrease Effects 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 230000001133 acceleration Effects 0.000 description 4
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 4
- 238000004523 catalytic cracking Methods 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- -1 alkaline earth metal salts Chemical class 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 239000010779 crude oil Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000002407 reforming Methods 0.000 description 3
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000001273 butane Substances 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000006073 displacement reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 239000002816 fuel additive Substances 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- ATQUFXWBVZUTKO-UHFFFAOYSA-N 1-methylcyclopentene Chemical compound CC1=CCCC1 ATQUFXWBVZUTKO-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241001573881 Corolla Species 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000006356 dehydrogenation reaction Methods 0.000 description 1
- 230000003009 desulfurizing effect Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000004231 fluid catalytic cracking Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000006078 metal deactivator Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000029058 respiratory gaseous exchange Effects 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011973 solid acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003556 thioamides Chemical class 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Description
本発明は、ガソリン組成物に関し、更に詳しくは、特定の成分を含む、高オクタン価で、吸気バルブの清浄性や運転性に優れ、環境保全性にも優れたガソリン組成物に関する。 The present invention relates to a gasoline composition, and more particularly to a gasoline composition containing a specific component, having a high octane number, excellent intake valve cleanliness and operability, and excellent environmental conservation.
近年、環境改善に対する関心が高まる中、自動車からの排出ガスの低減、燃費の改善等、環境性能に優れたものが要望されるようになってきた。燃費の改善を図るには、エンジンの圧縮比を高くして、熱効率を向上させる方法が知られている。しかし、圧縮比を高くするとノッキングが起こりやすくなるため、高オクタン価のガソリンが必要となる。 In recent years, with increasing interest in environmental improvement, there has been a demand for products with excellent environmental performance such as reduction of exhaust gas from automobiles and improvement of fuel consumption. In order to improve fuel efficiency, a method of increasing the compression ratio of an engine and improving thermal efficiency is known. However, if the compression ratio is increased, knocking is likely to occur, so gasoline having a high octane number is required.
一般に、高オクタン価ガソリンとして、重質で芳香族分含有量の多い高オクタン価基材を配合し、特定の蒸留性状及び成分組成を有するものが知られている(例えば、特許文献1参照)。また、シクロペンタン類を一定量配合して軽質分のオクタン価を向上させ、耐ノック性能を向上させたガソリン(例えば、特許文献2参照)や、メチルシクロペンテンを一定量配合した、オクタン価が高く、エンジンの出力性能に優れたガソリン(例えば、特許文献3参照)等が提案されている。しかし、これらのガソリンは、ガソリンエンジンの吸気バルブへのデポジットの付着性や、運転性等において未だ満足できない場合もあり、一層の改善が望まれる。 In general, as a high-octane gasoline, a high octane number base material having a heavy and high aromatic content and a specific distillation property and component composition are known (see, for example, Patent Document 1). In addition, gasoline with a certain amount of cyclopentane added to improve the octane number of light components and improved anti-knock performance (for example, see Patent Document 2), and a certain amount of methylcyclopentene compounded with a high octane number Has been proposed, such as gasoline (see, for example, Patent Document 3). However, these gasolines may still be unsatisfactory in terms of deposit adhesion to a gasoline engine intake valve, drivability, etc., and further improvements are desired.
本発明は、このような状況下で、ガソリン中の、環境保全上や吸気バルブへのデポジットに関し問題のある芳香族分を増加させることなく、ガソリンのオクタン価を向上させると共に、吸気バルブの清浄性、運転性を向上させ、環境保全性も向上させたガソリン組成物を提供することを目的とするものである。 Under such circumstances, the present invention improves the octane number of gasoline and increases the cleanliness of the intake valve without increasing the aromatic content in gasoline, which is problematic for environmental conservation and deposits on the intake valve. An object of the present invention is to provide a gasoline composition with improved drivability and improved environmental conservation.
本発明者らは、上記目的を達成するために鋭意研究を重ねた結果、2,4,4-トリメチル-1-ペンテンと2,4,4-トリメチル-2-ペンテンを所定量ガソリンに含有させることによって、上記目的を達成し得る優れた性能を有するガソリン組成物が得られることを見出し、更に、一定の成分組成や蒸留性状を有するようにすれば、より一層優れた性能のガソリン組成物が得られることを知見して、本発明を完成するに至った。
すなわち、本発明は、上記目的を達成するために、下記のガソリン組成物を提供する。
(1)BB留分を原料にして生成される留分を、2,4,4-トリメチル-1-ペンテンと2,4,4-トリメチル-2-ペンテンとを総和で0.5〜9容量%含有するように含有し、かつ以下の性状を満足することを特徴とするガソリン組成物。
(a)リード蒸気圧(RVP)が45〜90kPa
(b)リサーチ法オクタン価(RON)が89〜103
(c)50%留出温度(T50)が75〜110℃
(d)70℃留出量(E70)が18〜45容量%
(e)芳香族分含有量が5〜19.8容量%
(f)オレフィン分含有量が18〜30容量%
(g)ベンゼン含有量が1容量%以下
(h)硫黄分含有量が10質量ppm以下
As a result of intensive studies to achieve the above object, the inventors of the present invention contain 2,4,4-trimethyl-1-pentene and 2,4,4-trimethyl-2-pentene in a predetermined amount in gasoline. Thus, it is found that a gasoline composition having excellent performance capable of achieving the above-mentioned object can be obtained, and further, if it has a certain component composition and distillation properties, a gasoline composition with even better performance can be obtained. Knowing that it is obtained, the present invention has been completed.
That is, this invention provides the following gasoline composition in order to achieve the said objective.
(1) Containing 0.5 to 9 % by volume of 2,4,4-trimethyl-1-pentene and 2,4,4-trimethyl-2-pentene in fractions produced from BB fraction And a gasoline composition characterized by satisfying the following properties:
(A) Reed vapor pressure (RVP) 45 ~ 90kPa
(B) Research octane number (RON) is 89-103
(C) 50% distillation temperature (T50) is 75-110 ° C
(D) 70 ° C distillate (E70) is 18 to 45% by volume
(E) Aromatic content is 5-19.8 % by volume
(F) Olefin content is 18-30 % by volume
(G) Benzene content is 1% by volume or less (h) Sulfur content is 10 mass ppm or less
本発明のガソリン組成物は、自動車のガソリンエンジン用に好適であり、環境保全性に優れ、高オクタン価で、吸気バルブの清浄性や運転性に優れたものであり、実用性能を維持しつつ環境保全が図れるものである。 The gasoline composition of the present invention is suitable for an automobile gasoline engine, is excellent in environmental conservation, has a high octane number, and is excellent in cleanliness and drivability of an intake valve, while maintaining practical performance. It can be preserved.
以下、本発明の内容を更に詳しく説明する。 Hereinafter, the contents of the present invention will be described in more detail.
本発明のガソリン組成物に用いられる2,4,4-トリメチル-1-ペンテン、2,4,4-トリメチル-2-ペンテンは、その由来については特に制限はないが、BB留分を原料に、sec-ブチルアルコールを脱水素、精製してメチルエチルケトンを製造する工程から生成する2,4,4-トリメチル-1-ペンテン、2,4,4-トリメチル-2-ペンテンを含有する留分等を好ましく使用することができる。
BB留分を原料に、sec-ブチルアルコールの脱水素によるメチルエチルケトン製造工程から生成する留分は、一般に2,4,4-トリメチル-1-ペンテンや2,4,4-トリメチル-2-ペンテン以外に炭素数12のオレフィンなどを含んでおり、2,4,4-トリメチル-1-ペンテンと2,4,4-トリメチル-2-ペンテンの含有量は、両者の総和で、一般に25〜50容量%である。また、本発明では、従来から知られているいずれのメチルエチルケトン製造工程から生成する留分も、2,4,4-トリメチル-1-ペンテン、2,4,4-トリメチル-2-ペンテンを含有する限り使用することができる。
The origin of 2,4,4-trimethyl-1-pentene and 2,4,4-trimethyl-2-pentene used in the gasoline composition of the present invention is not particularly limited, but the BB fraction is used as a raw material. 2,4,4-trimethyl-1-pentene, fractions containing 2,4,4-trimethyl-2-pentene, etc. produced from the process of producing methyl ethyl ketone by dehydrogenating and purifying sec-butyl alcohol It can be preferably used.
The fraction produced from the methyl ethyl ketone production process using BB fraction as a raw material by dehydrogenation of sec-butyl alcohol is generally other than 2,4,4-trimethyl-1-pentene and 2,4,4-trimethyl-2-pentene. Contains 2,4,4-trimethyl-1-pentene and 2,4,4-trimethyl-2-pentene, the sum of both, generally 25-50 volumes %. In the present invention, the fraction produced from any conventionally known methyl ethyl ketone production process also contains 2,4,4-trimethyl-1-pentene and 2,4,4-trimethyl-2-pentene. As long as it can be used.
2,4,4-トリメチル-1-ペンテンはリサーチ法オクタン価(RON)が106、2,4,4-トリメチル-2-ペンテンはRONが103.5と高く、これらは、芳香族分ではないので、芳香族分が大きく影響する環境上の問題や吸気バルブのデポジットも少なく、オクタン価を向上させることができる物質である。 2,4,4-Trimethyl-1-pentene has a research octane number (RON) of 106, and 2,4,4-trimethyl-2-pentene has a high RON of 103.5, which is not an aromatic component. It is a substance that can improve the octane number with less environmental problems and the deposit of intake valves, which are greatly influenced by the family.
本発明のガソリン組成物においては、上記2,4,4-トリメチル-1-ペンテン、2,4,4-トリメチル-2-ペンテンの含有量は、両者の総和で、0.3〜10容量%である。この含有量が0.3容量%未満ではオクタン価の向上効果が十分に発揮されず、耐ノック性能、及び運転性が向上せず、10容量%を超えるとオレフィン分の増加によりガソリンの安定性が低下する可能性がある。オクタン価向上効果及び運転性等の点から、2,4,4-トリメチル-1-ペンテン、2,4,4-トリメチル-2-ペンテンの好ましい含有量は0.5〜9容量%である。また、2,4,4-トリメチル-1-ペンテンと2,4,4-トリメチル-2-ペンテンとの比率は特に制限されない。なお、2,4,4-トリメチル-1-ペンテン、2,4,4-トリメチル-2-ペンテンの含有量は、石油学会法JPI-5S-33-90(ガスクロマトグラフィー法)に準拠して測定した値である。 In the gasoline composition of the present invention, the contents of 2,4,4-trimethyl-1-pentene and 2,4,4-trimethyl-2-pentene are 0.3 to 10% by volume in total. . If the content is less than 0.3% by volume, the effect of improving the octane number is not sufficiently exerted, and the knocking resistance and drivability are not improved. If the content exceeds 10% by volume, the stability of the gasoline decreases due to an increase in the olefin content. there is a possibility. From the viewpoint of the octane number improving effect and the drivability, the preferable content of 2,4,4-trimethyl-1-pentene and 2,4,4-trimethyl-2-pentene is 0.5 to 9% by volume. Further, the ratio of 2,4,4-trimethyl-1-pentene and 2,4,4-trimethyl-2-pentene is not particularly limited. The contents of 2,4,4-trimethyl-1-pentene and 2,4,4-trimethyl-2-pentene are in accordance with JPI-5S-33-90 (gas chromatography method) of Petroleum Institute of Japan. It is a measured value.
本発明のガソリン組成物のリード蒸気圧(RVP)は、45〜90kPa、好ましくは50〜90kPaであることが望ましい。RVPを45kPa以上とすることで、低温始動性、暖気性の低下を防ぐことができ、90kPa以下とすることで、蒸発ガス量を少なくすることができて好ましい。なお、ここでRVPは、JIS K 2258に準拠して測定した値である。 The lead vapor pressure (RVP) of the gasoline composition of the present invention is 45 to 90 kPa, preferably 50 to 90 kPa. By setting RVP to 45 kPa or more, it is possible to prevent a decrease in low temperature startability and warming property, and setting to 90 kPa or less is preferable because the amount of evaporated gas can be reduced. Here, RVP is a value measured according to JIS K 2258.
本発明のガソリン組成物のリサーチ法オクタン価(RON)は、89〜103、好ましくは89〜102であることが望ましい。RONを89以上とすることで、高い運転性を維持することが可能となり、103以下とすることで、芳香族系の高オクタン価基材の配合量を抑えることができ、吸気バルブの清浄性の低下や、環境保全性の低下を防ぐことができて好ましい。なお、ここでRONは、JIS K 2280に準拠して測定した値である。 The research octane number (RON) of the gasoline composition of the present invention is desirably 89 to 103, preferably 89 to 102. By setting the RON to 89 or more, it becomes possible to maintain high operability. By setting the RON to 103 or less, the blending amount of the aromatic high octane base material can be suppressed, and the cleanliness of the intake valve is improved. It is preferable because it can prevent a decrease and a decrease in environmental conservation. Here, RON is a value measured in accordance with JIS K 2280.
本発明のガソリン組成物は、50%留出温度(T50)が75〜110℃、好ましくは80〜105℃、70℃留出量(E70)が18〜45容量%、好ましくは20〜42容量%であることが望ましい。T50及びE70が上記範囲内であれば、運転性、加速性に不具合を生じる場合を防ぐことができて好ましい。なお、これらの蒸留性状はJIS K 2254に準拠して測定した値である。 The gasoline composition of the present invention has a 50% distillation temperature (T50) of 75 to 110 ° C, preferably 80 to 105 ° C, and a 70 ° C distillation amount (E70) of 18 to 45% by volume, preferably 20 to 42 volumes. % Is desirable. If T50 and E70 are within the above ranges, it is preferable to prevent a case where a deficiency in drivability and acceleration performance occurs. These distillation properties are values measured in accordance with JIS K 2254.
本発明のガソリン組成物は、芳香族分含有量が45容量%以下、好ましくは5〜45容量%であることが望ましい。芳香族分含有量が45容量%以内であれば、排出ガス中の有害成分の増加を防ぐことができて好ましい。そして、オレフィン分含有量は30容量%以下、好ましくは5〜30容量%であることが望ましい。このオレフィン分含有量が30容量%以内であれば、酸化安定性の低下を防ぐことができて好ましい。なお、ここで芳香族分、オレフィン分は、石油学会法JPI-5S-33-90(ガスクロマトグラフ法)に準拠して測定した値である。 The gasoline composition of the present invention has an aromatic content of 45% by volume or less, preferably 5 to 45% by volume. If the aromatic content is within 45% by volume, an increase in harmful components in the exhaust gas can be prevented, which is preferable. The olefin content is 30% by volume or less, preferably 5 to 30% by volume. If the olefin content is within 30% by volume, a decrease in oxidation stability can be prevented, which is preferable. Here, the aromatic content and the olefin content are values measured in accordance with the Petroleum Institute method JPI-5S-33-90 (gas chromatographic method).
本発明のガソリン組成物は、ベンゼン含有量が1容量%以下、好ましくは0.8容量%以下であることが望ましい。ベンゼン含有量が1容量%以内であれば、大気中のベンゼン濃度の増加を防止し、環境汚染を低減できる可能性があって好ましい。なお、ここでベンゼン含有量は、石油学会法JPI-5S-33-90(ガスクロマトグラフ法)に準拠して測定した値である。 The gasoline composition of the present invention has a benzene content of 1% by volume or less, preferably 0.8% by volume or less. A benzene content of 1% by volume or less is preferable because it can prevent an increase in the concentration of benzene in the atmosphere and reduce environmental pollution. Here, the benzene content is a value measured according to the Japan Petroleum Institute method JPI-5S-33-90 (gas chromatographic method).
本発明のガソリン組成物は、硫黄分含有量が10質量ppm以下、好ましくは8質量ppm以下であることが望ましい。この硫黄分含有量が10質量ppm以内であれば、排出ガス浄化触媒の能力低下を防止し、排出ガス中のNOx、CO、THCの濃度上昇を防止できる可能性があって好ましい。なお、ここで硫黄分含有量は、JIS K 2541に準拠して測定した値である。 The gasoline composition of the present invention has a sulfur content of 10 ppm by mass or less, preferably 8 ppm by mass or less. If the sulfur content is within 10 ppm by mass, it is possible to prevent the exhaust gas purification catalyst from lowering its capacity and to prevent the concentration of NOx, CO and THC in the exhaust gas from increasing. Here, the sulfur content is a value measured in accordance with JIS K 2541.
上記のような性状を有するガソリン組成物を製造するために用いられるガソリン基材については、特に制限はないが、例えば、下記のような各種石油留分や化合物を基材として用いることができる。 Although there is no restriction | limiting in particular about the gasoline base material used in order to manufacture the gasoline composition which has the above characteristics, For example, the following various petroleum fractions and compounds can be used as a base material.
(イ)重質の直留ナフサなどを接触改質法(プラットフォーミング法、マグナフォーミング法、アロマイジング法、レニフォーミング法、フードリフォーミング法、ウルトラフォーミング法、パワーフォーミング法等)により、水素気流中で高温・加圧下で触媒(例えば、アルミナ担体に白金やロジウムと塩素とを担持したもの等)と接触処理して得られた改質ガソリンからベンゼン留分を蒸留により取り除いた脱ベンゼン接触改質ガソリン。 (B) Hydrogen stream by contact reforming method (Platforming method, Magnaforming method, Aromaizing method, Reforming method, Food reforming method, Ultraforming method, Powerforming method, etc.) for heavy straight-run naphtha, etc. In which the benzene fraction is removed by distillation from a reformed gasoline obtained by contact treatment with a catalyst (for example, platinum, rhodium and chlorine supported on an alumina carrier) at high temperature and pressure. Quality gasoline.
(ロ)上記接触改質法により接触処理して得られた改質ガソリンを蒸留により、軽質留分、ベンゼン留分、重質留分に分けた内の軽質留分(脱ベンゼン軽質接触改質ガソリン)及び重質留分(脱ベンゼン重質接触改質ガソリン)。 (B) The reformed gasoline obtained by contact treatment by the above catalytic reforming method is separated into light fraction, benzene fraction, and heavy fraction by distillation. Gasoline) and heavy fractions (debenzene heavy catalytic reforming gasoline).
(ハ)灯・軽油から常圧残油に至る石油留分、好ましくは重質軽油や減圧軽油を、従来から知られている接触分解法、特に流動接触分解法(UOP法、シェル二段式法、フレキシクラッキング法、ウルトラオルソフロー法、テキサコ法、ガルフ法、ウルトラキャットクラッキング法、RCC法、HOC法等)により、固体酸触媒(例えば、シリカ・アルミナにゼオライトを配合したもの等)で分解して得られた接触分解ガソリン、それを蒸留して得られる軽質接触分解ガソリン。 (C) Petroleum fraction ranging from kerosene / light oil to atmospheric residual oil, preferably heavy gas oil or vacuum gas oil, is conventionally known catalytic cracking method, especially fluid catalytic cracking method (UOP method, shell two-stage type) Decomposition with a solid acid catalyst (eg, silica / alumina blended with zeolite, etc.) by the method, flexi cracking method, ultra ortho flow method, texaco method, gulf method, ultra cat cracking method, RCC method, HOC method, etc. Catalytically cracked gasoline obtained as a result, lightly cracked gasoline obtained by distilling it.
(ニ)イソブタンと低級オレフィン(ブテン、プロピレン等)を原料として、酸触媒(硫酸、フッ化水素、塩化アルミニウム等)の存在下で反応させて得られるアルキレート。 (D) An alkylate obtained by reacting isobutane and a lower olefin (butene, propylene, etc.) in the presence of an acid catalyst (sulfuric acid, hydrogen fluoride, aluminum chloride, etc.).
(ホ)原油を常圧蒸留した直留ナフサを脱硫処理して得られた脱硫直留ナフサを蒸留により、軽質留分と重質留分に分けた軽質留分(軽質ナフサ)。 (E) Light distillate (light naphtha) obtained by distilling desulfurized straight naphtha obtained by desulfurizing straight-run naphtha obtained by atmospheric distillation of crude oil into light and heavy fractions by distillation.
(ヘ)原油や粗油等の常圧蒸留時、改質ガソリン製造時、あるいは分解ガソリン製造時等に蒸留して得られるブタン、ブテン類を主成分としたC4留分。 (F) C4 fractions mainly composed of butane and butenes obtained by distillation during the atmospheric distillation of crude oil or crude oil, during the production of reformed gasoline, or during the production of cracked gasoline.
(ト)直鎖の低級パラフィン系炭化水素の異性化によって得られるアイソメレート、あるいはアイソメレートを精密蒸留して得られるイソペンタン、接触改質ガソリンから得られるトルエン、キシレン、あるいは炭素数9以上の芳香族を主体とする留分等。 (G) Isomerate obtained by isomerization of straight-chain lower paraffin hydrocarbons, or isopentane obtained by precision distillation of isomerate, toluene, xylene obtained from catalytically reformed gasoline, or fragrance having 9 or more carbon atoms Dividends mainly composed of tribes.
上記のような各種留分を基材として用いて、前記各組成、性状を満たすように、該各種留分の性状等に応じて配合量を適宜選択して、適宜配合することにより本発明の無鉛ガソリンを製造することができる。 Using the various fractions as described above as a base material, the blending amount is appropriately selected according to the properties of the various fractions and the like so as to satisfy the respective compositions and properties. Unleaded gasoline can be produced.
本発明のガソリン組成物には、更に必要に応じて、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、フェノール系、アミン系等の酸化防止剤、チオアミド化合物等の金属不活性剤、有機リン系化合物等の表面着火防止剤、コハク酸イミド、ポリアルキルアミン、ポリエーテルアミン、ポリイソブテンアミン等の清浄分散剤、長鎖脂肪族エステル・アミン等の摩擦調整剤、多価アルコール及びそのエーテル等の氷結防止剤、有機酸のアルカリ金属やアルカリ土類金属塩、高級アルコールの硫酸エステル等の助燃剤、アニオン系界面活性剤、カチオン系界面活性剤、両性界面活性剤等の帯電防止剤、アルケニル琥珀酸エステル等の錆止め剤及びアゾ染料等の着色剤等、公知の燃料添加剤が挙げられる。これらを1種又は数種組み合わせて添加することができる。これら燃料添加剤の添加量は任意であるが、通常、その合計添加量が0.1重量%以下とすることが好ましい。 Various additives can be appropriately blended in the gasoline composition of the present invention as necessary. Such additives include phenolic and amine antioxidants, metal deactivators such as thioamide compounds, surface ignition inhibitors such as organophosphorus compounds, succinimides, polyalkylamines, polyetheramines. , Detergents and dispersants such as polyisobuteneamine, friction modifiers such as long chain aliphatic esters and amines, antifreezing agents such as polyhydric alcohols and their ethers, alkali metals and alkaline earth metal salts of organic acids, sulfuric acid of higher alcohols Known fuel additives such as esters, etc., anionic surfactants, cationic surfactants, antistatic agents such as amphoteric surfactants, rust inhibitors such as alkenyl succinates, and colorants such as azo dyes Is mentioned. These can be added singly or in combination. The addition amount of these fuel additives is arbitrary, but usually the total addition amount is preferably 0.1% by weight or less.
以下に本発明の内容を実施例及び比較例により更に詳しく説明するが、本発明はこれらによって制限されるものではない。 The content of the present invention will be described in more detail with reference to Examples and Comparative Examples below, but the present invention is not limited thereto.
(実施例1〜4、比較例1〜4)
接触分解装置、接触改質装置、常圧蒸留装置などから生成するC4留分(ブタン、ブテン類)、表1に示す性状の脱ベンゼン接触改質ガソリン(基材A)、脱ベンゼン軽質接触改質ガソリン(基材B)、脱ベンゼン重質接触改質ガソリン(基材C)、接触分解ガソリン(基材D)、軽質接触分解ガソリン(基材E)、アルキレート(基材F)、軽質ナフサ(基材G)、及び2,4,4-トリメチル-1-ペンテン・2,4,4-トリメチル-2-ペンテンを含有する留分(基材H)を表2に示す配合比で配合することにより、表2に記載する性状のガソリンを得た。さらに、得られたガソリンについて清浄性試験と運転性試験を行い、その結果を表2に示した。清浄性試験と運転性試験は下記のように行った。
(Examples 1-4, Comparative Examples 1-4)
C4 fractions (butane, butenes) produced from catalytic cracking equipment, catalytic reforming equipment, atmospheric distillation equipment, etc., properties of debenzene catalyzed reformed gasoline (base material A), debenzene light catalytic reforming properties shown in Table 1 Quality gasoline (base material B), debenzene heavy catalytic reforming gasoline (base material C), catalytic cracking gasoline (base material D), light catalytic cracking gasoline (base material E), alkylate (base material F), light Blends naphtha (base G) and fractions containing 2,4,4-trimethyl-1-pentene and 2,4,4-trimethyl-2-pentene (base H) in the blending ratios shown in Table 2. As a result, gasoline having the properties shown in Table 2 was obtained. Furthermore, cleanliness tests and operability tests were performed on the obtained gasoline, and the results are shown in Table 2. The cleanability test and the operability test were performed as follows.
(清浄性試験)
排気量1.5L、マルチポイントインジェクション(MPI)方式の車輌を用い、シャシーダイナモにおいて、60−100km/hの加減速×1,500サイクル(8,000km走行)の条件で行い、吸気弁に付着したデポジット(IVD)の目視による評価(Rating:CRC(Coordinating Research Council)No.16)を実施した。なお、このRating値は、数値が大きい方がIVD量は少ないことを示す。
(Cleanliness test)
Using a 1.5L displacement, multipoint injection (MPI) type vehicle, the chassis dynamo accelerated and decelerated at 60-100km / h x 1,500 cycles (running 8,000km) and deposited on the intake valve (IVD ) Was visually evaluated (Rating: CRC (Coordinating Research Council) No. 16). This Rating value indicates that the larger the numerical value, the smaller the IVD amount.
(運転性試験)
試験車輌には、トヨタ カローラ(エンジン:5E-FE、排気量:1,496cc)を用いた。車輌をシャシーダイナモ上に設置し、温度20±3℃、湿度50±5%の条件下で10時間ソークした後、エンジンを始動した。エンジン始動後、アクセル開度50%の条件で、0−40km/hの加速を冷機条件から20回繰り返した。
(Drivability test)
Toyota Corolla (engine: 5E-FE, displacement: 1,496cc) was used as the test vehicle. The vehicle was placed on the chassis dynamo and soaked for 10 hours under the conditions of temperature 20 ± 3 ℃ and humidity 50 ± 5%, and then the engine was started. After starting the engine, acceleration of 0-40km / h was repeated 20 times from the cold condition under the condition of 50% accelerator opening.
運転性評価については、石油学会“2005年度運転性調査結果報告書”に記載の方法に準拠し、アイドリング期間中や加速中に発生した不具合について、以下に記す不具合の係数とデメリット評点の積の総和として求め、その現象の程度から運転性の優劣を決定した。 The drivability evaluation conforms to the method described in the Petroleum Institute “FY2005 Drivability Survey Results Report”. For defects that occurred during the idling period or during acceleration, the product of the following failure coefficient and disadvantage score Obtained as the sum, the superiority or inferiority of driving performance was determined from the degree of the phenomenon.
デメリット現象としては、アイドル安定性、走行中における前後の振動、加速のもたつき、息つき、バックファイヤ、アイドル時エンジンストール、走行時エンジンストールを対象とし、その係数をそれぞれ、1、4、6、6、6、8、32とした。 Disadvantages include idle stability, front / rear vibration during driving, acceleration stagnation, breathing, backfire, engine stall during idling, engine stall during running, and the coefficients are 1, 4, 6, respectively. 6, 6, 8, 32.
また、現象の程度をテストドライバーでないと判別できない場合をデメリット評点1、平均的なドライバーが判別できる程度をデメリット評点2、どのドライバーでも指摘する程度をデメリット評点4とした。 Also, demerit score 1 when the degree of phenomenon can only be determined by a test driver, demerit score 2 when the average driver can be identified, and demerit score 4 when any driver points out.
なお、評価は、不具合が全く発生せずデメリット点数が0の場合を◎、デメリット点数が1〜20の場合を△、デメリット点数が21以上の場合を×として実施した。 The evaluation was carried out with ◎ when the disadvantage did not occur at all and the disadvantage score was 0, Δ when the disadvantage score was 1 to 20, and x when the disadvantage score was 21 or more.
以上の結果から、本発明のガソリン組成物は、吸気バルブの清浄性、及び運転性に優れ、実用性能を維持しつつ大気環境の保全が図れるものであることは明らかである。 From the above results, it is clear that the gasoline composition of the present invention is excellent in cleanliness and operability of the intake valve, and can maintain the atmospheric environment while maintaining practical performance.
Claims (1)
(a)リード蒸気圧(RVP)が45〜90kPa
(b)リサーチ法オクタン価(RON)が89〜103
(c)50%留出温度(T50)が75〜110℃
(d)70℃留出量(E70)が18〜45容量%
(e)芳香族分含有量が5〜19.8容量%
(f)オレフィン分含有量が18〜30容量%
(g)ベンゼン含有量が1容量%以下
(h)硫黄分含有量が10質量ppm以下 The fractions generated by the BB fraction to the raw material, so as to contain 0.5 to 9% by volume total and 2,4,4-trimethyl-1-pentene and 2,4,4-trimethyl-2-pentene A gasoline composition containing and satisfying the following properties:
(A) Reed vapor pressure (RVP) 45 ~ 90kPa
(B) Research octane number (RON) is 89-103
(C) 50% distillation temperature (T50) is 75-110 ° C
(D) 70 ° C distillate (E70) is 18 to 45% by volume
(E) Aromatic content is 5-19.8 % by volume
(F) Olefin content is 18-30 % by volume
(G) Benzene content is 1% by volume or less (h) Sulfur content is 10 mass ppm or less
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JP5350742B2 (en) * | 2008-10-14 | 2013-11-27 | Jx日鉱日石エネルギー株式会社 | Method for producing gasoline composition |
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US9834492B2 (en) | 2012-11-12 | 2017-12-05 | Uop Llc | Process for fluid catalytic cracking oligomerate |
US9914673B2 (en) | 2012-11-12 | 2018-03-13 | Uop Llc | Process for oligomerizing light olefins |
US10508064B2 (en) | 2012-11-12 | 2019-12-17 | Uop Llc | Process for oligomerizing gasoline without further upgrading |
WO2014074833A1 (en) | 2012-11-12 | 2014-05-15 | Uop Llc | Process for making gasoline by oligomerization |
US9522375B2 (en) | 2012-11-12 | 2016-12-20 | Uop Llc | Apparatus for fluid catalytic cracking oligomerate |
US9644159B2 (en) | 2012-11-12 | 2017-05-09 | Uop Llc | Composition of oligomerate |
US9522373B2 (en) | 2012-11-12 | 2016-12-20 | Uop Llc | Apparatus for oligomerizing light olefins |
US9567267B2 (en) | 2012-11-12 | 2017-02-14 | Uop Llc | Process for oligomerizing light olefins including pentenes |
US9441173B2 (en) | 2012-11-12 | 2016-09-13 | Uop Llc | Process for making diesel by oligomerization |
US9663415B2 (en) | 2012-11-12 | 2017-05-30 | Uop Llc | Process for making diesel by oligomerization of gasoline |
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