首页> 外国专利> MESOPOROUS AND MACROPOROUS CATALYST WITH ACTIVE PHASE OBTAINED BY COMULLING, METHOD FOR PREPARING SAME AND USE THEREOF FOR HYDROTREATMENT OF RESIDUUM

MESOPOROUS AND MACROPOROUS CATALYST WITH ACTIVE PHASE OBTAINED BY COMULLING, METHOD FOR PREPARING SAME AND USE THEREOF FOR HYDROTREATMENT OF RESIDUUM

机译:精制得到的具有活性相的介孔和宏观催化剂,其制备方法及其用于渣油的加氢处理

摘要

FIELD: chemistry.;SUBSTANCE: invention relates to a mesoporous and macroporous hydroconversion catalyst with an active phase, to a method of producing said catalyst, as well as to a method of hydrotreating a heavy hydrocarbon feedstock. Hydroconversion catalyst comprises a matrix of calcined aluminum oxide and an active hydrodehydrogenation phase comprising at least molybdenum as a group VIB metal of the Periodic Table of elements, in some cases at least nickel or cobalt as a Group VIII metal of the Periodic Table of Elements, in some cases phosphorus. Active phase is completely introduced by mixing by means of combined rubbing, with said matrix. Catalyst is characterized by specific surface area SBET more than 100 m2/g, median mesopore diameter from 12 to 25 nm, including range boundaries, median macropore diameter from 50 to 250 nm, including the range of the mesopore volume, greater than or equal to 0.65 ml/g, total pore volume greater than or equal to 0.75 ml/g, and macropore volume of 15–35 % of the total pore volume. Method of producing catalyst comprises first step of depositing in aqueous reaction medium at temperature in range of 20 to 90 °C for a period of time from 2 minutes to 30 minutes. Further, suspension is heated to temperature in range from 40 to 90 °C for time of 7 minutes to 45 minutes. Thereafter, a second step of depositing the suspension is carried out at a temperature in range from 40 to 90 °C for a period of time from 2 minutes to 50 minutes. Suspension is then filtered to obtain an aluminum oxide gel. Thereafter, aluminum oxide gel is dried to produce powder. Then, heat treatment stage of powder is performed at temperature from 500 to 1000 °C for a period of time from 2 to 10 hours, in the presence or absence of an air stream containing up to 60 vol. %. water to obtain calcined porous aluminum oxide. Thereafter, a burnt porous aluminum oxide and a solution of at least one metal precursor of the active phase is co-blended to obtain a paste. Then, produced paste is formed. Thereafter, molded paste is dried at temperature less than or equal to 200 °C, to produce dried catalyst. If necessary, the stage of thermal treatment of the dried catalyst is carried out at a temperature lying in range from 200 to 1000 °C, in the presence or absence of water. Method of hydrotreating heavy hydrocarbon feedstock consists in that hydrocarbon raw material is brought in contact with hydrogen and said catalyst.;EFFECT: invention enables to obtain a catalyst having a large volume of mesopores combined with a large volume of macropores, increased diameter of mesopores and an active phase of hydrodehydrogenation.;18 cl, 9 tbl, 8 ex
机译:技术领域本发明涉及具有活性相的中孔和大孔加氢转化催化剂,所述催化剂的生产方法以及加氢处理重质烃原料的方法。加氢转化催化剂包括煅烧氧化铝的基体和活性加氢脱氢相,该活性加氢脱氢相至少包含钼作为元素周期表的VIB族金属,在某些情况下至少包含镍或钴作为元素周期表的VIII族金属,在某些情况下,磷。活性相通过组合摩擦与所述基质混合而完全引入。催化剂的特征是比表面积S BET 大于100 m 2 / g,中孔直径中位数为12至25 nm,包括范围边界,中孔直径中位数为50至250 nm,包括中孔体积的范围,大于或等于0.65 ml / g,总孔体积大于或等于0.75 ml / g,大孔体积为总孔体积的15–35%。制备催化剂的方法包括第一步,其在20至90℃的温度下在水性反应介质中沉积2分钟至30分钟的时间。此外,将悬浮液加热到40至90°C的温度持续7分钟至45分钟的时间。此后,在40至90℃的温度下进行沉积悬浮液的第二步,时间为2分钟至50分钟。然后将悬浮液过滤以获得氧化铝凝胶。之后,将氧化铝凝胶干燥以产生粉末。然后,在存在或不存在高达60体积的气流的情况下,在500至1000°C的温度下进行粉末的热处理阶段2至10小时。 %。用水获得煅烧的多孔氧化铝。此后,将燃烧过的多孔氧化铝和至少一种活性相的金属前体的溶液共混以获得糊剂。然后,形成生产的糊剂。之后,将成型的糊状物在小于或等于200°C的温度下干燥,以生产干燥的催化剂。如有必要,可以在有水或无水的情况下,在200至1000℃的温度范围内对干燥的催化剂进行热处理。加氢处理重质烃原料的方法包括使烃原料与氢气和所述催化剂接触。效果:本发明能够获得具有大量中孔和大量大孔,增加的中孔直径和加氢脱氢的活性相。; 18 cl,9 tbl,8 ex

著录项

  • 公开/公告号RU2686697C2

    专利类型

  • 公开/公告日2019-04-30

    原文格式PDF

  • 申请/专利权人 IFP ENERGIES NOUVELLES;

    申请/专利号RU20170100947

  • 申请日2015-06-09

  • 分类号B01J23/74;B01J23/88;B01J23/75;B01J21/04;B01J27/18;B01J37/03;B01J37/04;B01J37/08;B01J37/16;B01J37/20;B01J35/10;C10G45/08;

  • 国家 RU

  • 入库时间 2022-08-21 11:46:14

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