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Improved process for the regeneration of catalysts used in reforming hydrocarbons

机译:用于重整烃的催化剂的再生的改进方法

摘要

PICT:0600802/III/1 In reforming hydrocarbons in presence of a reforming catalyst and added hydrogen at superatmospheric pressure with periodic regeneration of the catalyst, the same is subjected after regeneration to a purging operation with hydrogen or hydrogen-containing gas at a pressure substantially less than that of the reforming. A virgin naphtha may, for example, be heated above 950 DEG F. in heater 5 and fed by line 10, together with hydrogen from line 11 to converter 12 containing trays of catalyst, preferably molybdena on activated alumina. Pressure is preferably 150-400 p.s.i. The product leaves by line 20, gases containing hydrogen being recovered in separator 42 and recycled by line 30 to line 11, if desired after removing hydrocarbons. Bottoms pass by line 43 to fractionator 44 where the desired product is recovered, bottoms being recycled, and overhead treated to recover hydrogen for re-use. Catalyst regeneration is effected by closing valve 31, purging with hydrogen or recycled gas fed through line 33 and leaving by line 35, and the injecting air, preferably at 600-700 DEG F., from line 41 at a pressure about the same as that used in the reforming whereby deposits are burnt off the catalyst which is at a temperature of about 900 DEG F. The inert flue gases leave by pipe 35 or may be in part recycled by line 46, with additional flue gas from line 41. Pressure is now reduced to atmospheric by taking off flue gas, preferably over a period of 5-15, say 6 minutes, when valve 32 is opened and recycle, hydrogen-containing gas is passed through the converter 12 for about 30 minutes and discarded through line 35. At the end of this period, no hydrogen should be consumed by the catalyst. The valve in line 35 is now closed and recycle gas pumped into the converter for about 8 minutes until the reaction pressure is again reached. The purging may, however, be effected at sub-atmospheric pressure or up to about 50 p.s.i.ALSO:PICT:0600802/IV(b)/1 In reforming hydrocarbons in presence of a reforming catalyst and added hydrogen at superatmospheric pressure with periodic regeneration of the catalyst, the same is subjected after regeneration to a purging operation with hydrogen or hydrogen-containing gas at a pressure substantially less than that of the reforming. A virgin naphtha may, for example, be heated above 950 DEG F. in heater 5 and fed by line 10 together with hydrogen from line 11 to converter 12 containing trays of catalyst, preferably molybdena on activated alumina. Pressure is preferably 150-400 p.s.i. The product leaves by line 20, gases containing hydrogen being recovered in separator 42 and recycled by line 30 to line 11, if desired after removing hydrocarbons. Bottoms pass by line 43 to fractionator 44 where the desired product is recovered, bottoms being recycled, and overhead treated to recover hydrogen for re-use. Catalyst regeneration is effected by closing valve 31, purging with hydrogen or recycled gas fed through line 33 and leaving by line 35, and then injecting air, preferably at 600-700 DEG F., from line 41 at a pressure about the same as that used in the reforming, whereby deposits are burnt off the catalyst which is at a temperature of about 900 DEG F. The inert flue gases leave by pipe 35 or may be in part recycled by line 46, with additional flue gas from line 41. Pressure is now reduced to atmospheric by taking off flue gas, preferably over a period of 5-15, say 6 mins., when valve 32 is opened and recycle, hydrogen-containing gas is passed through the converter 12 for about 30 mins. and discarded through line 35. At the end of this period, no hydrogen should be consumed by the catalyst. The valve in line 35 is now closed and recycle gas pumped into the converter for about 8 mins. until the reaction pressure is again reached. The purging may, however, be effected at sub-atmospheric pressure or up to about 50 p.s.i. The invention is illustrated by the conversion of methylcyclohexane to toluene.
机译:在重整催化剂存在下重整烃类并在超大气压下加入氢气并定期再生催化剂的情况下,再生后将其在氢气或含氢气体下进行净化操作。压力大大低于重整压力。例如,可以将原始石脑油在加热器5中加热到950°F以上,并通过管线10与氢气一起从管线11进料到含有催化剂塔板的转化器12,所述催化剂塔板优选为在活性氧化铝上的钼。压力优选为150-400p.s.i。产物通过管线20离开,如果需要,在除去烃之后,将含氢的气体在分离器42中回收,并通过管线30再循环至管线11。底部馏出物通过管线43到达分馏器44,在其中回收所需产物,将底部馏出物再循环,并进行塔顶处理以回收氢气以供再次使用。催化剂的再生是通过关闭阀31,用经管线33供入的氢气或再循环气体吹扫并经管线35排出,以及最好以约600-700°F的压力从管线41以大约相同的压力注入空气来进行的。用在重整过程中,从而在约900°F的温度下将沉积物从催化剂上烧掉。惰性烟道气通过管道35排出,或者可以部分通过管线46再循环,另外的烟道气则来自管线41。现在通过排出烟气将其降低到大气中,最好是在5-15分钟(例如6分钟)内,当阀32打开并循环使用时,含氢气体通过转化器12大约30分钟并通过管线35排出在此期间结束时,催化剂不应消耗氢。现在关闭管线35中的阀门,并将循环气体泵入转炉约8分钟,直到再次达到反应压力。但是,吹扫可在低于大气压或最高约50 psi的压力下进行。ALSO:在重整催化剂存在下重整烃类并在超大气压下定期加入氢气催化剂再生后,在再生后用氢气或含氢气体在实质上小于重整压力的压力下进行净化操作。例如,可以将原始石脑油在加热器5中加热到950°F以上,并通过管线10与氢气一起从管线11进料到包含催化剂塔盘的转化器12,所述催化剂塔盘优选是在活性氧化铝上的钼。压力优选为150-400p.s.i。产物通过管线20离开,如果需要,在除去烃之后,将含氢的气体在分离器42中回收,并通过管线30再循环至管线11。底部馏出物通过管线43到达分馏器44,在其中回收所需产物,将底部馏出物再循环,并进行塔顶处理以回收氢气以供再次使用。催化剂的再生是通过关闭阀31,用经管线33送入的氢气或再循环气体吹扫并由管线35排出,然后从管线41以优选大约600-700°F的压力注入空气,优选以600-700°F进行的。在重整过程中使用,从而将沉积物从温度约为900°F的催化剂上烧掉。惰性烟道气通过管道35排出,或者可以部分地通过管线46再循环,另外的烟道气则来自管线41。压力现在通过排出烟气将其还原成大气,优选地在5-15的时间段内,例如6分钟,当阀32打开并再循环时,含氢气体通过转化器12约30分钟。并通过管线35丢弃。在此期间结束时,催化剂不应消耗氢。现在关闭管线35中的阀门,并将循环气体泵入转炉约8分钟。直到再次达到反应压力。但是,吹扫可以在低于大气压或高达约50p.s.i的条件下进行。通过甲基环己烷到甲苯的转化来说明本发明。

著录项

  • 公开/公告号GB600802A

    专利类型

  • 公开/公告日1948-04-20

    原文格式PDF

  • 申请/专利权人 STANDARD OIL DEVELOPMENT COMPANY;

    申请/专利号GB19430010993

  • 发明设计人

    申请日1943-07-06

  • 分类号B01J23/90;B01J38/12;C10G35/22;

  • 国家 GB

  • 入库时间 2022-08-24 02:39:23

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