离子液体在燃料油脱硫中的应用研究
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摘要
随着世界环保法规的日趋严格,世界各国对燃料油品中的硫含量提出了更严格的要求。与其他脱硫技术相比,离子液体萃取脱硫技术工艺简单,条件温和,可以在不改变燃料油组分的情况下脱除燃料油油中的硫化物,这些特点使基于离子液体的萃取技术具有良好的应用前景。
     本文合成了[HMim]Cl/CuCl、[Et3HN]Cl/CuCl离子液体,代替传统的[AMim]+离子,用[HMim]Cl/CuCl离子液体和[Et3HN]Cl/CuCl离子液体进行络合萃取脱硫,研究了离子液体的种类、反应时间、反应温度等工艺条件对脱硫率的影响,汽油脱硫率分别达到86.1%和86.8%。
     目前国内外萃取脱硫所使用的离子液体大部分是咪唑类离子液体,而使用其他离子液体的研究鲜见报道。本文研究了吡啶类离子液体对汽油的萃取脱硫性能,当阴离子相同时,阳离子取代基越大脱硫效果越好;当阳离子相同时,并不是阴离子越大脱硫效果越好,还与阴离子的性质有关;同时还研究了吡啶离子液体萃取-氧化汽油脱硫的情况。
     将臭氧高级氧化技术与离子液体萃取相结合,用于FCC汽油氧化-萃取脱硫实验,脱硫率可达87.5%;OH-的加入对离子液体中的臭氧氧化过程有促进作用。使用Br?nsted酸性离子液体萃取-氧化柴油中的含硫化合物,其中Br?nsted酸性离子液体[Hnmp]BF4既是萃取剂,又是催化剂。[Hnmp]BF4可以从油相中萃取DBT,H2O2与离子液体的阳离子形成配合物,然后分解产生自由羟基基团,被萃取到离子液体体系中的DBT被自由羟基氧化成二苯并噻吩砜,油相中不含有硫的氧化产物。将该体系应用于真实柴油的脱硫过程中,脱硫率达到99.4%,表明[Hnmp]BF4离子液体-H2O2体系可以用于柴油的深度脱硫。
Along with more attention being paid to environment protection worldwide, most countries have made laws or regulations to restrict the sulfur content in fuel oil with a more rigorous standard. Among these techniques, the extraction desulfurization with ionic liquids, which has many advantages such as low investment, simple techniques, mild conditions, easy separation etc, shows promising as an approach for the deep desulfurization of fuel oil.
     Several lower cost ionic liquid, such as [Et3HN]Cl/CuCl and [HMim]Cl/CuCl, were prepared and characterized. The effect of experiment condition to desulfurizaiton rate was researched. The sulfur removal were 86.1% and 86.8% respectively when [HMim]Cl/CuCl and [Et3HN]Cl/CuCl ionic liquid were used for extraction desulfurization.
     In previous researches, ionic liquids employed to desulfurize from fuels are mostly N-alkylimidazolim-based ionic liquids. In this thesis, N-alkyl-pyridinium-based ionic liquids were used in extractive desulfurization. The properties of N-alkyl-pyridinium-based ionic liquids were studied for the first time. The desulfurization ability of ionic liquids connects with the chemical property of ionic liquids, such as the cation or anion structure, size of ionic liquids. With the same anion, increase of cation size by the substitution of a longer alkyl group to the pyridium ring was responsible for the increase of the extractive capacity for thiophene. But a similar phenomenon did not hold with increasing anion size when the cations of ionic liquids were same; desulfurization ability of ILs connects with the chemical property of anion. We also researched the extraction-oxidation desulfurization with N-alkyl-pyridinium-based ionic liquids.
     Extraction/Oxidation with ionic liquids and O3 are combined to desulfurize the sulfur compound in FCC gasoline. The desulfurization rate could reach 87.5%. O3 oxidation process could be promoted by the addiation of OH-.
     Br?nsted ionic liquid [Hnmp]BF4 was used to be a catalyst and extractant for desulfurization of model oil and actual diesel fuel. In this process, DBT was oxidized in the ionic liquid phase as it was extracted from oil phase, so a continuous decrease in the concentration of DBT in n-octane was observed for each solvent during the oxidation process. [Hnmp]BF4 is not only the extractant but also the catalyst. One of its catalytic roles is to decompose hydrogen peroxide to form hydroxyl radicals. DBT in the ionic liquids phase was oxidized to its corresponding sulfone by the hydroxyl radicals. Sulfone did not exist in the oil phase because of the high polarity of ionic liquid. DBT sulfone can be detected in the ionic liquid phase.In addition, the ionic liquid was also effective on the ODS of actual diesel fuel. 99.4% sulfur-containing compounds which present in the actual diesel fuel can be removed. The results show that ionic liquids [Hnmp]BF4 could be used in deep desulfurization.
引文
[1]刘伯华,姚国欣,廖健,创新的炼油技术,当代石油化工,2001,12(9): 27-33
    [2]崔文广,周二鹏,赵地顺,催化裂化汽油脱硫技术进展,河北工业科技,2004, 21(2): 1-4
    [3]王天普,催化裂化汽油脱硫技术进展,齐鲁石油化工,2001,29(1): 48-51
    [4]郑嘉惠,清洁染料生产技术评述,当代石油化工,2003,11(1):4-6
    [5] Shihs S, Owensp J, Mobil’soctga in process: FCC gasoline desulfurization reaches a new performance level, National Petrochemical and Refiners Association Annual Meeting, San Antonio: 1999, 30-37
    [6] Drake C A, Love S D. Process for desulfurization and aromatizing hydrocarbons [ P ]. US Patent: 6 083 379, 2000
    [7] Martinezn P, Salazarj A, Tegada J. Meet gasoline pool sulfur and octane targets with the ISAL process, National Petrochemical and Refiners Association Annual Meeting, Washington, 2000, 52-61
    [8] Judzis A, Peninger S, Deteter J C, et al, Start-up of first CDHDS unit atmotiva’s port Arthur, Texas refinery, National Petrochemical and Refiners Association Annual Meeting , New Orleans, 2001, 11-17
    [9] Tippett T, Ultra low sulfur diesel: catalyst and process options, National Petrochemical and Refiners Association Annual Meeting, San Antonio, 1999, 6-13
    [10]李春义,山红红,杨朝合等,汽油催化裂化脱硫催化剂,中国专利: 200 120 711, 2000
    [11] Wormsb Echer RF, Kim G. Sulfur reduction in FCC gasoline [ P ]. US Patent: 5 376 608, 1994
    [12] Wormsb Echer R, Kin G, Sulfur reduction in FCC gasoline [ P ]. US Patent: 5525210, 1996
    [13]柯明,范志明,轻质油品非加氢脱硫进展,石油与天然气化工,1997,2(26): 100– 104
    [14] Irviner L, Process for desulfurizing gasoline and hydrocarbon feeds tocks , US Patent: 5 730 860, 1998
    [15] Irviner L, Bensonb A, Varraveto D M, Irvad process low cost breakthrough for low sulfur gasoline, National Petrochemical and Refiners Association Annual Meeting, San Antonio, 1999, 42-48
    [16] Gyanesh P, Bartlesvill E, Desulfurization and novel sobents for same, US Patent: 6346190, 2002.
    [17]路景双,孙发民,赵建航,等.国内外汽柴油现状及发展趋势[J ] .应用能源技术,2001 , (3) :8 - 9.
    [18] Monticello D J, Biodesulfurization of diesel fuels, Chem Tech, 1998, 28(7):38 -45
    [19] Jiangc Y, Liu H, Biodesulfurization of Dibenzothiophene by the Strain of Nocardia Globerular, Proceedings of Third Joint China/ USA. Chemical Engineering Conference, 2000, 119 - 122
    [20]姜成英,王蓉,刘会洲等,石油和煤微生物脱硫技术的研究进展,过程工程学报,2001,1(1):80 - 85
    [21] Yu L Q, Meyer T A, Flosom B R. Oil/ water/ biocatalyst three phase separation process, US Patent: 5772901 ,1998
    [22] Grossman M J, Lee M K, Prince R C, Microbiol desulfurization of a crude oil middle2distillate fraction: analysis of the extent of sulfer remove and the effect of removal on remaining sulfur, Appl Environ Microbio, 1999, 65:181 - 188
    [23] Otsuki S, Nonaka T, Takashima N, et al, Oxidative desulfurization of light gas oil and vacuum gas oil by oxidation and solvent extraction, Energy Fuels, 2000, 6 (14): 1232 - 1239
    [24] Shiraishi Y, Tachibana K, Hirai T, et al, Desulfurization and denitrogenation process for light oils based on chemical oxidation follow ed by liquid - liquid extraction, Ind Eng Chem Res, 2002, 41(71): 4362 - 4375
    [25] Shiraishi Y, Tachibana K, Hirai T, et al, Photochemical production of biphenyls from oxidized sulfur compounds obtained by oxidative desulfurization of light oils , Energy Fuels, 2003, 17 (1): 95 - 100
    [26] Otsuki S, Nonaka K, Takashima N, et al, Oxidative desulfurization of middle distillate-oxidation of dibenzothiophene using t-butyl hypo chlorite, Sekiyu gakkaishi, 2001, 44(1): 20-23
    [27] Wang D H, Qian W H, Amano H, et al, Oxidative desulfurization of fuel oil Part I. Oxidation of dibenzothiophenes using tert-butyl hydroperoxide, Appl Catal A: General, 2003, 253(1): 91 - 99
    [28] Avidan A, Cullen M, Sulphc co-desulfurization via selective oxidation pilot plant results and commercialization plans, National Petrochemical and Refiners Association Annual Meeting , New Orleans, 2001, 55-59
    [29] Mei H, Mei B W, Yen T F, A new method for obtaining ultra - low sulfur diesel fuel via ultrasound assisted oxidative desulfurization, Fuel, 2003, 82 (4): 405 - 414
    [30] Shiraishi Y, Tachibana K, Hirai T, et al, Visible light - induced desulfurization process for catalytic cracked gasoline using an organic two - phase extraction sys tem, Ind Eng Chem Res, 1999, 38 (12): 4538 - 4544
    [31] Shiraishi Y, Tachibana K, Hirai T, et al, Visible light - induced desulfurization process for light oils by photochemical electron - transfer oxidation in an organic two - phase extraction system, Ind Eng Chem Res, 1999, 38 ( 9): 3310 -3318
    [32] Hiral T, Shiraishi Y, Komsava I, Desulfurization process for light oil by photochemical reaction and liquid - liquid extraction: removal of benzothiophenes and alkyl sulfides, J Chem Eng J ap, 1997, 30 (1): 173 - 175.
    [33] Kabe T, Ishihara A, Tajima H, Hydrodesulfurization of sulfur - containing polyaromatic compounds in light oil, Ind Eng Chem Res, 1992, 31 (6): 1577 - 1580
    [34] Hiral T, Shiraishi Y, Komsava I, Desulfurization process for benzothiophenes from light oil by photochemical reaction and liquid - liquid extraction , Ind Eng Chem Res, 1996, 35 (2): 586 - 589
    [35] Hiral T, Shiraishi Y, Ogawa K, et al, Effect of photosensitizer and hydrogen peroxide on desulfurization of light oil by photochemical reaction and liquid - liquid extraction, Ind Eng Chem Res, 1997, 36 (3): 530 - 533
    [36] Liu W Y, Lei Z L, Wang J K, Kinetics and mechanism of plasma oxidative desulfurization in liquid phase, Energy Fuels, 2001, 15 (1): 38 - 43
    [37]王豪,唐晓东,周建军等,柴油氧化脱硫技术研究进展,石油与天然气化工,2003,32 (1) : 38241
    [38]杨金荣,侯影飞,孔瑛等,柴油臭氧氧化脱硫研究,石油大学学报(自然科学版),2002,26(4): 86291
    [39] Sotsuki T, Takashimaetal N, Oxidation desulfurization of light gas oil and vacuum gas oil by oxidation and solvent extraction, Energy Fuels, 2000, 14:1232 - 1239
    [40] Horii Y, Onuki H, Doi S, et al. Desulfurization of light oil by extraction, US:5494572 ,1996
    [41] Funakoshi R, Miyadad M, et al. Process for covering organic sulfur compounds from fuel oil , US: 5753102 ,1998 [42 ]杨丽娜,由宏君,王强,萃取法脱除催化裂化柴油中的酸性硫化物,辽宁化工,2003,32(11):489 - 492.
    [43] Thomas W, Room-Temperature Ionic Liquids: Solvents for Synthesis and Catalysis, Chem. Rev., 1999, 99(8): 2071-2083
    [44] Jairton D, Crestina S. Consorti et al, Room Temperature Molten Salts: Neoteric“Green”Solvents for Chemical Reactions and Processes, J. Braz. Soc., 2000, 11(4): 337-344
    [45]杨绮琴,方北龙,常温熔盐体系,化学通报,1993,5:14-22
    [46]李汝雄,王建基,室温离子液体的合成与应用,化学试剂,2001,23(4):211-215
    [47]李雪辉,徐键昌,王乐夫等,室温离子液体,现代化工,2001,21(8):58-63
    [48] Fuller J, Carlin R T, Long D et al, Structure of 1-ethl-3-methyl-imidazolium hexafluorophosphate: made for room temperature molten salts, J. Chem. Soc. Chem. Commun., 1994, (2), 299-301
    [49] Hurley F H, Wier T P, Electrodeposition of Metals from Fused Quaternary Ammonium Salts, J. Electrochem. Soc., 1951, 98(2): 203-208
    [50] Wiles J S, Zaworotko M. J, Air and water stable 1-ethyl-3-methylimidazolium based ionic liquids, Chem. Commun. 1992, (13), 965-967
    [51] McGuinness D S, Saendig N, Yates B F et al, Kinetic and density functional studies on alkyl-carbene elimination from Pd(II) heterocylic carbene complexes: a new type of reductive elimination with clear implications for catalysis, J Am Chem Soc, 2001, 123(17): 4029-4040
    [52] McGuinness D S, Cavell K J, Yates B F, et al. Oxidative addition of the imidazolium cation to zerovalent Ni, Pd, and Pt: a combined density functional and experimental study, J Am Chem Soc, 2001, 123(34): 8317―8328
    [53] Chaumont A, Wipff G, Solvation of uranyl(II) and europium(III) cations and their chloro complexes in a room-temperature ionic liquid. A theoretical study of the effect of solvent“humidity”, Inorg Chem, 2004, 43(19): 5891―5901
    [54] Gaillard C, Azzi A, Billard I, et al, Uranyl complexation in fluorinated acids (HF, HBF4, HPF6, HTf2N): A combined experimental and theoretical study, Inorg Chem, 2005, 44(4): 852―861
    [55] Katsyuba S A, Dyson P J, Vandyukova E E, et al, Vidis Ana. Molecular structure, vibrational spectra, and hydrogen bonding of the ionic liquid 1-ethyl-3-methyl-1H-imidazolium tetrafluoroborate, Helv Chim Acta, 2004, 87: 2556―2565
    [56] Jeson P J, Ellis D J, Welton T, Parker D G. Arene hydrogenation in a room-temperature ionic liquid using a ruthenium cluster cata phasic protocol, J Mol Catal A: Chem, lyst. Chem Commun, 1999, (1), 25-26
    [57] Ellis D J, Dyson P J, Parker D G, et al, Arene hydrogenation in a room-temperature ionic liquid using a ruthenium cluster catalyst, Chem.Commun., 1999, 150: 71-75
    [58] Herrmann W A, Bohm V P, Heck Reaction Catalyzed by Phospha -palladacycles in Non-aqueous Ionic Liquids, J. Organomet. Chem., 1999, 572:141-145
    [59] Mathews C J, Smith P J, Welton T, Palladium Catalysed Suzuki Cross - coupling Reactions in Ambient Temperature Ionic Lliquids, Chem. Commun., 2000, (14): 1249-1250
    [60] Matsumoto H, Kageyama H, Miyazaki Y, Room Temperature Ionic Liquids Based on Small Aliphatic Ammonium Cations and Asymmetric Amide Anions, Chem. Commun., 2002, (16):1726–1727
    [61] Howerth J, Hanlon K, Fayne D, et al, Moisture Stable Dialkylimidazolium Salts as Heterogeneous and Homogeneous Lewis Acids in The Diels-alder Reaction. Tetrahedron Lett., 1997, 38(17), 3097–3100
    [62] Fuller J, Carlin R T. Facile Preparation of Tetrafluoroborate and Trifluoromethanesulfonate Room-temperature Ionic Liquids, Proc. Electrochem. Soc., 1998, 2:227–230
    [63] Song C E, Diels-alder Reactions in Chloroaluminate Ionic Liquids: Acceleration and Selectivity Enhancement, Tetraheron Lett.,1999, 40(14):2461–2464
    [64] Song C E, Oh C R, Roh E J, et al. Cr(salen) Catalysed Asymmetric Ring Opening Reactions of Epoxides in Room Temperature Ionic Liquids, Chem.Commun., 2000, (18):1743–1748
    [65] Song C E, Roh E J. Ractical Method to Recycle A Chiral(salen)Mn Epoxidation Catalyst by Using an Ionic Liquid, Chem.Commun., 2000, (10):837–838
    [66] Cull S G, Holbrey J D, Vargas-Mora V, et al, Room Temperature Ionic Liquids as Replacements for Organic Solvents in Multiphase Bioprocess Operations, Biotechnol. Bioeng., 2000, 69(2):227–233
    [67] Erbeldinger M, Mesiano A J, Russeu A J, Enzymatic Catalysis of Formation of Z-Aspartame in Ionic Liquid—An Alternative to Enzymatic Catalysis in Organic Solvents, Biotechnol. Progr., 2000, 16:1129–1131
    [68] Huddleston J G, Willauer H D, Swatloski R P, et al, Chem Commun, 1998, (16): 1765~1766
    [69] Cull S G, Holbrey J D, Vargas-Mora V, et al, Room-temperature ionic liquids as replacements for organic solvents in multiphase bioprocess operations , Biotechnology and Bioengineering, 2000, 69(2): 227~233
    [70] Swatloski R. P., Spear S. K., Holbrey J. D. et al, Dissolution of Cellulose with Ionic Liquids, J. Am. Chem. Soc., 2002, 124(18), 4974–4975.
    [71] Dai S, Ju Y H, Barnes C E, Solvent extraction of strontium nitrate by a crown ether using room-temperature ionic liquids, Chem Soc, Dalton Trans, 1999,(8): 1201~1202
    [72] Dullius J E L, Suarez Paulo A Z, Einloft S, et al, Selective Catalytic Hydrodimerization of 1,3-Butadiene by Palladium Compounds Dissolved in Ionic Liquids, Organnometallics, 1998, 17(5): 815~819
    [73] Blanchard L A, Hancu D, Beckman E J, et al, Green processing using ionic liquids and CO2, Nature, 1999, 399(6731): 28~29
    [74] Macfarlane D R,Huang J,Forsyth M, Lithium- doped plastic crystal electrolytes exhibiting fast ion conduction for secondary batteries. Nature,1999, 402:792- 794.
    [75] Bockirs J O, Reddy A, Gambca- Aldeco M. Modern electrochemistry (1)- ionics , New York: Kluwer Academic Publishers, 2002
    [76] KochV R, Nanjundiah C, Appetecchi G B, The interfacial stability of Li with two new solvent - free ionic liquids: 1,2- dimethyl- 3- propylimidazolium imide and methide, J Electrochem Soc, 1995,142(7): L 116- L 118
    [77] Yasushi K, Isamu K, Takashi M, et al, Redox reaction in 1- ethyl- 3- methyl imidazolium- iron chlorides molten salt system for battery application, J Power Sources, 2002,109 (2):327- 3 321
    [78] Yasuhiko I, Toshiyuki N. Non- conventional electrolytes for electrochemical applications, Electrochimica Acta, 2000, 45(15- 16): 2 611- 2 622
    [79] Fuller J, Osteryoung R A, Carlin R T, Rechargeable lithium and sodium anodes in chloroaluminate molten saltscontaining thionyl chloride, J Electrochem Soc,1995,142(11): 3632- 3636
    [80] Abbott A P, Capper G, Swain B G, et al, Electropolishing of stainless steel in an ionic liquid, Transaction of the Institute of Metal Finshing, 2005,83(1):51- 53
    [81] Takaya s, Maruo T, Marukane S, et al, Electrochemical properties of novel ionic liquids for electric double layer capacitor applications, Journal of Power Sources, 2004,138:253- 261
    [82] Balducci Andrea, Henderson Wesley A, Simon Patrice, etal, Cycling stability of a hybrid activated carbon / poly (3 -methylthiophene) supercapacitor with N– methylpyrrolidinium bis (trifluromethanesulfonyl) imide ionic liquid, Electrochemica Acta, 2005, 50(11):2 233- 2 237
    [83] BuzzeoMarisa C, Hardacre C, Compton R G, Use of room temperature ionic liquids in gas sensor design, Analytical Chemistry, 2004, 76(15): 4 583- 4 588.
    [84] Bōsmann A, Daatsevich L, Jess A, et al. Deep desulfurization of diesel fuel by extraction with ionic liquids, Chem. Commun., 2001, 2494–2495
    [85] Zhang S G, Zhang Z C, Novel properties of Ionic Liquids in Selective Sulfur Removal from Fuels at Room Temperature, Green Chemistry, 2002, 98(4): 376–379
    [86] Zhang S G, Zhang Z C, Extractive Desulfurization and Denitrogenation of Fuels Using Ionic Liquids, Ind. Eng. Chem. Res., 2004, 77(43): 614-622
    [87] Huang C P, Chen B H, Zhang J, Desulfurization of Gasoline by Extraction with New Ionic Liquids, Energy Fuels, 2004, 18(6): 1862-1864
    [88] E?er J, Wasserscheid P, Jess A, Deep desulfurization of oil refinery streams by extraction with ionic liquids, Green Chem., 2004, 6(7), 316-322
    [89] Lo W H, Yang H Y, Wei G T, One-pot desulfurization of light oils by chemical oxidation andsolvent extraction with room temperature ionic liquids, Green Chem., 2003, 5(6): 639-642
    [90] Su B M, Zhang S G, Zhang Z Z, Structural Elucidation of Thiophene Interaction with Ionic Liquids by Multinuclear NMR Spectroscopy, J. Phys. Chem. B, 2004, 108 (50), 19510 -19517
    [91] Nie Y, Li C X, Sun A J, Extractive Desulfurization of Gasoline Using Imidazolium-Based Phosphoric Ionic Liquids, Energy & Fuels, 2006, 20 (5), 2083–2087
    [92] Nie Y, Li C X, Wang Z H, Extractive Desulfurization of Fuel Oil Using Alkylimidazole and Its Mixture with Dialkylphosphate Ionic Liquids, Ind. Eng. Chem. Res., 2007, 46 (15), 5108 -5112
    [93]王玉新,李丹东,曹祖宾等,室温氯铝酸离子液体络合吸附噻吩类硫化物的研究,石油化工高等学校学报,2004,17(4):42-46
    [94]冯婕,李春喜,孟洪等,磷酸酯类离子液体在燃油深度脱硫中的应用,石油化工,2006,35(3):272-276
    [95]张傑,黄崇品,陈标华,用[BMim][Cu2Cl3]离子液体萃取脱除汽油中的硫化物,燃料化学学报,2005,33 (4):431-434
    [96]张成中,黄崇品,李建伟,离子液体的结构及其汽油萃取脱硫性能,化学研究,2005,(16):23-25
    [97]周瀚成,陈楠,石峰,离子液体萃取脱硫新工艺研究,分子催化,2005,19(2): 94-97
    [98]张进,朴香兰,朱慎林,离子液体对燃油含硫化合物的萃取性能研究,化学试剂,2006,28 (7):385~387
    [99]蒋小川,于春影,冯婕等,离子液体1-丁基-3-甲基咪唑磷酸二丁酯的制备与应用,北京化工大学学报2006 34 (1): 5-7
    [100] Huang C P, Chen B H, Zhang J, Desulfurization of Gasoline by Extraction with New Ionic Liquids, Energy Fuels, 2004, 18(6): 1862-1864
    [101]王玉新,李丹东,袁秋菊,室温离子液体对噻吩硫化物的络合吸附工艺,辽宁化工,2004,33(9):512-514
    [102] Schoonover R E, Oxidation-extraction removal of organosulfur compounds from hydrocarbon fuels by contact with ionic liquids. U.S. Pat. Appl. Publ. 2003085156, 2003-05-08
    [103]亓西敏,张爱健,张贵荣等,噻吩在离子液体中的电化学聚合及其在汽油脱硫中的应用,环境化学, 2006,25(2):183-186
    [104]黄蔚霞,李云龙,汪燮卿,离子液体在催化裂化汽油脱硫中的应用,化工进展,2004,23(3):297-299
    [105]苗树运,张洪庆,曹祖宾等,室温离子液体脱除直馏柴油中碱性氮化物,石油化工高等学校学报,2006,19(2):9-12
    [106] Kwak C, Lee J J, Bae J S al. Hydrodesulfurization of DBT, 4-MDBT, and 4,6-DMDBT on fluorinated CoMoS/Al2O3 catalysts, Applied Catalysis A: General, 2000, 200(2): 233-242
    [107] Raheel S, Hutchings G J, Hydrodesulfurization of hindered dibenzothiophenes: an overview, Catalysis Today, 2000, 59(4):423-442
    [108] Ma X, Sakanishi K, Mochida I, Hydrodesulfurization reactivities of various sulfur compounds in diesel fuel, Ind. Eng. Chem. Res., 1994, 34(2):218-222
    [109]叶天旭,张予辉,刘金河等,离子液体降低FCC汽油烯烃体积分数的研究,燃料化学学报,2005,33(2):175 - 178
    [110] Holbrey J. D., Reichert W. M., Sheppard O., Rogers R. D., Liquid clathrate formation in ionic liquid-aromatic mixtures. Chem. Commun. 2003, (4) :467-477
    [111]赵地顺,马四国,刘翠微等,相转移催化应用于催化裂化汽油氧化脱硫的研究,高等学校化学学报,2006,27(1):144~146
    [112]赵地顺,任红威,马四国等,催化裂化汽油的相转移催化氧化脱硫反应研究,化学学报,2006,64(20):2086~2090
    [113]江举辉,虞继舜,李武等,臭氧协同产生·OH的高级氧化过程研究进展及影响因素的探讨,工业安全与环保,2001,27(12):16-20
    [114]胡莉蓉,国内外柴油氧化脱硫技术研究进展,化工时刊,2004,18(8):17~19
    [115] Kazumasa Y, Takeshi F, Keiji Mi,et al, Tungstophosphoric Acid-catalyzed Oxidative Desulfurization of Light Oil with Hydrogen Peroxide in a Light Oil/Acetic Acid Biphasic System, Chem. Lett.,2003,32(10): 920~921
    [111]凌昊,沈本贤,高玉廷等,提高H2O2/甲酸体系选择性氧化抽提脱硫效率的研究,华东理工大学学报,2003,29(4):351~354
    [117] Zhu H P, Yang F, Tang J, et al. Br?nsted acidic ionic liquid 1-methylimidazolium tetrafluoroborate: A green catalyst and recyclable medium for esterification , Green Chemistry, 2003, 5(1), 38–39
    [118] Cooper M S, Heaney H, Newbold A J, et al, Oxidation Reactions Using Urea-Hydrogen Peroxide: A Safe Alternative to Anhydrous Hydrogen Peroxide, Synlett, 1990, (9): 533-535

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