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Co-coking of Hydrotreated Decant Oil/Coal Blends: Effect of Hydrotreatment Severity on the Yield Distribution and Quality of Distillate Fuels

机译:加氢精制油/煤共混物的共焦化:加氢深度对馏分燃料产率分布和质量的影响

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摘要

The co-coking of hydrotreated decant oil (DO)/coal blends using a large laboratory-scale delayed coker was studied. DO was hydrotreated at several levels of severity for use in the co-coking work. Increasing the hydrotreatment severity increased the levels of hydrodesulfurization (from 50.6 to 99.0%) and hydrodenitrogenation (from 7.7 to 88.7%). Hydrotreatment resulted in increased amounts of paraffins, saturated cyclics, alkylbenzenes, two-ring aromatics, and hydroaromatics but decreased the amount of three-ring and larger compounds in the liquid. The coke yield from delayed co-coking of hydrotreated DOs and coal blends was observed to be in the range of 15.9-24.4%. Distillate liquid obtained from delayed co-coking increased with hydrotreating severity of DOs (from 71.0 to 76.2%). The boiling point distribution of the distillate liquid products was determined using fractional vacuum distillation. The results from vacuum distillation reveal that the percentage of the liquid products corresponding to jet fuel and diesel boiling ranges increases with an increasing hydrotreatment level. Characterization of gasoline, jet fuel, and diesel fractions was conducted using gas chromatography/mass spectroscopy (GC/MS). The GC/MS results of the gasoline fractions indicate a dominance of paraffins, saturated cyclics, and benzenes. Characterization of the jet fuel fractions shows that two-ring aromatics and hydroaromatics are present in the fuel in addition to paraffins, saturated cyclics, and benzenes. No polycyclic aromatic compounds were observed in jet fuel fractions. The diesel fuel fraction was mostly comprised of alkyl-substituted benzenes, naphthalenes, and three-ring and larger (more condensed) compounds.
机译:研究了使用大型实验室规模的延迟焦化器对加氢处理的倾析油(DO)/煤混合物进行共焦化的方法。在共焦化工作中,对DO进行了几种严重程度的加氢处理。加氢处理的严重程度增加,加氢脱硫(从50.6%增至99.0%)和加氢脱氮(从7.7%增至88.7%)的水平。加氢处理导致链烷烃,饱和环,烷基苯,二环芳族化合物和加氢芳族化合物的量增加,但液体中三环及较大化合物的数量减少。观察到加氢的溶解氧和煤共混物的延迟焦化产生的焦炭产率为15.9-24.4%。延迟焦化得到的馏出液随DO加氢处理的严重程度的增加而增加(从71.0%增至76.2%)。使用分馏真空蒸馏确定馏出液体产物的沸点分布。真空蒸馏的结果表明,与喷气燃料和柴油沸程相对应的液体产物的百分比随着加氢处理水平的提高而增加。使用气相色谱/质谱(GC / MS)对汽油,喷气燃料和柴油馏分进行表征。汽油馏分的GC / MS结果表明,石蜡,饱和环和苯占主导地位。喷气燃料馏分的特征表明,除了链烷烃,饱和环和苯之外,燃料中还存在二环芳烃和氢芳烃。在喷气燃料馏分中未观察到多环芳族化合物。柴油馏分主要由烷基取代的苯,萘和三环及更大(更稠合)的化合物组成。

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  • 来源
    《Energy & fuels》 |2013年第mayajuna期|3071-3079|共9页
  • 作者单位

    The Earth and Mineral Sciences (EMS) Energy Institute, The Pennsylvania State University, University Park, Pennsylvania 16802, United States;

    Leslie R. RIIdnick: Ultrachem Incorporated, 900 Centerpoint Boulevard, New Castle, Delaware 19720, United States;

    The Earth and Mineral Sciences (EMS) Energy Institute, The Pennsylvania State University, University Park, Pennsylvania 16802, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
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