首页> 外国专利> IMPROVED METHOD OF REFINING COAL BY SHORT RESIDENCE TIME HYDRODI SPROPORTIONATION TO FORM A NOVEL COAL DERIVED FUEL SYSTEM

IMPROVED METHOD OF REFINING COAL BY SHORT RESIDENCE TIME HYDRODI SPROPORTIONATION TO FORM A NOVEL COAL DERIVED FUEL SYSTEM

机译:短时滞水力配比精炼煤形成新型煤衍生燃料系统的改进方法

摘要

The present invention is directed to an improved process for refining coal by short residence time hydro disproportionation reactions to produce slate of fluid phase fuel systems and useful crude products.;In another aspect, the present invention is directed to an improved process for converting useful hydrogen while producing large amounts of liquid hydrocarbons by short residence time partial liquid sulfur.;It can be readily seen that the short residence time hydro- disproportionation (SRT-HDP) process can be carried out at a higher heating rate without causing gas formation and / or condensation reactions at low pressures and high volatilization temperatures. According to the invention, particles of volatile-containing carbonaceous material are heated at a rate effective to rapidly decompose and volatilize the solid organic material. The decomposition reaction volatilizes the solid organic material into hydrocarbon fractions and free radicals, which are released as carbonaceous particles. This volatilized hydrocarbon fraction is in intimate contact with a gas-reducing atmosphere containing a large amount of hydrogen donor at a hydrogenation temperature effective to promote hydrogenation of the fraction and free radical hydrogen capping. Although hydrocracking occurs (depending on the hydrogenation temperature), the hydrogenation temperature and hydrogenation residence time are chosen to reduce thermal hydrocracking and vaporization.;The particles are rapidly heated to a volatilization temperature to decompose solid organics and then hydrogenated at a hydrogenation temperature to produce stable and good hydrocarbon liquids from the hydrogen produced therein while minimizing condensation reactions and gas production. Accordingly, the heating rate can be increased to increase the decomposition reaction rate, while the hydrogenation temperature is selected to carry out an efficient hydrogenation reaction of the decomposition product without promoting secondary vaporization and / or decomposition reactions.;The process of the present invention includes an improved process for refining a carbonaceous material containing volatiles to produce a hydrocarbon-containing product by means of a short residence time hydro disproportionation reaction. The method considers a heating step of rapidly heating volatile-containing carbonaceous particles to a volatile temperature effective to produce decomposition and volatile products at a rate effective to minimize condensation and charcoal formation. The decomposed product is contacted with a hydrogen donor-containing gas atmosphere at a hydrogenation temperature to undergo decomposition and hydrogen camping of the volatilized material. Hydrogenation is achieved with a residence time effective to complete the hydrogenation of the fragments. The hydrogenated material is then cooled to a stabilization temperature below the reaction temperature to prevent degradation of the liquid product into the gas by thermal hydrocracking.;The heating rate in the heating step is to optimize the decomposition reaction rate. Contact of the volatilized material with a large amount of hydrogen donor gas reducing atmosphere is carried out under hydrogenated conditions of the decomposed volatile material.;In a preferred embodiment, a large amount of hydrogen donor-containing gas reducing atmosphere is obtained from the carbonaceous material in substantial portions. In one embodiment, the hydrogen donor high content gas and / or hydrogen is present in the HDP mixed gas. In another embodiment, the atmosphere containing a large amount of hydrogen donor is used as the first cooling stream to reduce to temperatures below the decomposition temperature and to the hydrogenation temperature. According to another preferred embodiment, the hydrogenation material is further cooled to stabilize, ie to prevent further hydrocracking and / or condensation of the liquid.;In another embodiment, the hydrocarbon-containing cracked steam from the hydro disproportionation reaction is partially cooled to the hydrogenation temperature by contacting the steam with the steaming component which is recovered from the hydrocarbon vapor and recycled in the presence of a large amount of hydrogen donor gas reducing atmosphere. This initial cooling, in addition to reducing the temperature of the cracked steam, increases the temperature of the steam to a temperature high enough to thermally crack the steam via diesel. Preferably, the temperature of the steam is reduced to a stabilization temperature using a second cooling medium which may comprise water recovered from the hydrocarbon vapor and circulating light oil. In a very preferred embodiment, a partial oxidation reactor is used to generate a gas atmosphere containing a large amount of heat and hydrogen donor for volatilization / decomposition.;In another embodiment, the use of a short residence time reaction produces more hydrocarbon liquid by producing petroleum substitutes and chemical feedstocks at lower pressures and higher volatilization temperatures with faster heating rates without causing incidental gas generation and / or condensation reactions. Let's do it.;In another embodiment, the catalyst is introduced with feed coal or intermediate cooling gas to increase the liquid hydrocarbon yield and to obtain a good halogenated oil product.;In another embodiment, the catalyst may be introduced or mixed with the partially hydrogenated hydrocarbon bottom stream of the charcoal separator at a temperature and residence time effective for further hydrogenation. Preferably, the reaction product from the liquefaction is cooled to the hydrogenation temperature using hydrogen or a hydrogen containing gas. The hydrogen-rich vapor and the hydrogenation temperature provide conditions ideal for catalytic hydrogenation of liquid hydrocarbons.;In another embodiment, a liquefaction reactor containing methane or a large amount of methane containing other light hydrocarbons in an amount effective to delay the formation of methane and other light hydrocarbons from the carbonaceous feedstock with the carbonaceous feed material or with the hot feed gas. Can be introduced in Short residence time The addition of methane in the reactor significantly reduces the conversion of hydrocarbon feedstock to methane and increases the liquid hydrocarbon yield, thus significantly reducing hydrogen consumption.
机译:本发明涉及通过短停留时间加氢歧化反应以生产液相燃料系统和有用的原油产物的板岩的精炼煤的改进方法。另一方面,本发明涉及转化有用的氢的改进方法。 ;很容易看出,短停留时间加氢歧化(SRT-HDP)工艺可以在较高的加热速率下进行,而不会引起气体形成和/在低压和高挥发温度下发生缩合反应。根据本发明,以有效地使固体有机材料快速分解和挥发的速率加热含挥发性碳质材料的颗粒。分解反应将固体有机物质挥发成烃馏分和自由基,并以碳质颗粒的形式释放出来。该挥发的烃馏分在有效促进馏分的氢化和自由基氢封端的氢化温度下,与含有大量氢供体的还原性气氛紧密接触。尽管发生加氢裂化(取决于氢化温度),但选择氢化温度和氢化停留时间以减少热加氢裂化和汽化。;将颗粒快速加热至挥发温度以分解固体有机物,然后在氢化温度下氢化以产生由其中产生的氢气产生的稳定,优质的烃类液体,同时最大程度地减少了缩合反应和气体的产生。因此,可以提高加热速率以增加分解反应速率,同时选择氢化温度以进行分解产物的有效氢化反应而不促进二次蒸发和/或分解反应。通过短停留时间加氢歧化反应,精制包含挥发物的碳质材料以产生含烃产物的改进方法。该方法考虑了加热步骤,该加热步骤将含挥发性的碳质颗粒快速加热至挥发性温度,该挥发性温度有效地以最小化冷凝和木炭形成的速率产生分解和挥发性产物。分解的产物在氢化温度下与含氢供体的气体气氛接触,以使挥发的物质分解和残留在氢中。氢化以有效完成碎片氢化的停留时间实现。然后将氢化的材料冷却至低于反应温度的稳定温度,以防止液体产物因热加氢裂化而降解为气体。加热步骤中的加热速率旨在优化分解反应速率。在分解的挥发性材料的氢化条件下,使挥发的材料与大量的氢供体气体还原气氛接触。在一个优选的实施方案中,从碳质材料获得大量的含氢供体气体还原气氛。大部分。在一实施方案中,在HDP混合气体中存在氢供体高含量气体和/或氢。在另一个实施方案中,将包含大量氢供体的气氛用作第一冷却流以降低至低于分解温度的温度和降至氢化温度。根据另一个优选的实施方案,将氢化材料进一步冷却以稳定,即防止液体进一步加氢裂化和/或冷凝。在另一个实施方案中,将来自氢歧化反应的含烃裂化蒸汽部分冷却至氢化通过使蒸汽与从烃蒸汽中回收并在大量的氢供体气体还原气氛下再循环的蒸汽成分接触而达到最高温度。除了降低裂解蒸汽的温度之外,这种初始冷却还将蒸汽的温度提高到足以通过柴油热裂解蒸汽的温度。优选地,使用第二冷却介质将蒸汽的温度降低至稳定温度,该第二冷却介质可以包括从烃蒸气回收的水和循环的轻油。在一个非常优选的实施方案中,使用部分氧化反应器产生包含大量热和氢供体的气体气氛以进行挥发/分解。因此,使用短停留时间反应可在较低的压力和较高的挥发温度下以更快的加热速率生产石油代用品和化学原料,从而产生更多的烃类液体,而不会引起附带的气体生成和/或冷凝反应。在另一实施方式中,将催化剂与进料煤或中间冷却气体一起引入,以增加液态烃的收率并获得良好的卤代油产物。在另一实施方式中,可以将催化剂引入或与部分催化剂混合在有效进行进一步氢化的温度和停留时间下,木炭分离器的氢化烃塔底物流。优选地,使用氢或含氢气体将液化的反应产物冷却至氢化温度。富氢蒸气和氢化温度为液体烃的催化氢化提供了理想的条件。在另一个实施方案中,液化反应器包含甲烷或大量包含其他轻质烃的甲烷,其数量有效地延迟了甲烷的生成和来自含碳原料的其他轻质烃,含碳原料或热原料气。可以在短停留时间内引入。在反应器中添加甲烷可显着降低烃类原料向甲烷的转化率,并提高液态烃类收率,从而显着减少氢气消耗。

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