首页> 外国专利> A PROCEDURE FOR THE SELF-HYDROGENATION OF REFINERY GASES, FROM CATALYTIC FLUIDS CRACKING FACILITIES AND DELAYED COKING FACILITIES

A PROCEDURE FOR THE SELF-HYDROGENATION OF REFINERY GASES, FROM CATALYTIC FLUIDS CRACKING FACILITIES AND DELAYED COKING FACILITIES

机译:从催化流裂化装置和延迟焦化装置进行炼制气自加氢的程序

摘要

PT--81622 A Process comprises (a) sepg. liq. stream from a refinery gas stream (A) , the liq.-free gas stream being split into a stream (B) feeding a fuel gas system and a stream (C) making up an ammonia plant feed (b) passing stream C through a compressor suction drum and compressing, causing intermediate suction of satd. and cooled gas recycle and mixing of gas with feed and removing portion of reaction-generated heat from hydrogenation reactor (c) compressing gas from (b) at 100-713 psi (7-50 kg/sq.cm) or higher, pref. 385-713 psi (27-50 kg/sq. cm), forming stream (D), the compressor receiving low density gases with a high concn. of H2 from cracking of heavy gas oil and vacuum residue with high levels of Ni (d) heating stream recovering heat from the recycle, effluent from hydrogenation reactor, passing mixt. (E) feed-recycle gas through reactor, the feed-recycle gas ratio being controlled so that the temp. of reactor is kept at min. levels of coke deposits on the catalyst without reduction in the hydrogenation reaction rate, reactor being filled with a fixed bed catalyst of cobalt-molybdenum oxide or Ni-Mo, and designed so that the space velocity is such that the hydrogenated prod. stream (F) is practically olefin-free or ultimately contains below 0.3 wt.% olefins, the life-time of the catalyst being at least a year and at the same time S cpds. e.g. COS, being hydrogenated to sulphydric acid (e) passing a portion of hydrogenated gas, stream (G), through a ZnO fixed bed reactor to remove as ZnS the sulphydric acid in the refinery gas or produced is (d) followed by injection of the hydrogenated and S-free refinery gas, stream (K), in the water stream reformer (f) returning a portion of hydrogenated gas, stream (H), to heat exchanger, cooling the gas, stream (I), with water up to 140-170 (150) deg. C, sepg. liq. formed followed by injection of gas, stream (I), in intermediate stage of compressor. (First major country equivalent to PT--81622-A) GBAB- GB2183670 B Process comprises (a) sepg. liq. stream from a refinery gas stream (A) , the liq.-free gas stream being split into a stream (B) feeding a fuel gas system and a stream (C) making up an ammonia plant feed (b) passing stream C through a compressor suction drum and compressing, causing intermediate suction of satd. and cooled gas recycle and mixing of gas with feed and removing portion of reaction-generated heat from hydrogenation reactor (c) compressing gas from (b) at 100-713 psi (7-50 kg/sq.cm) or higher, pref. 385-713 psi (27-50 kg/sq. cm), forming stream (D), the compressor receiving low density gases with a high concn. of H2 from cracking of heavy gas oil and vacuum residue with high levels of Ni (d) heating stream recovering heat from the recycle, effluent from hydrogenation reactor, passing mixt. (E) feed-recycle gas through reactor, the feed-recycle gas ratio being controlled so that the temp. of reactor is kept at min. levels of coke deposits on the catalyst without reduction in the hydrogenation reaction rate, reactor being filled with a fixed bed catalyst of cobalt-molybdenum oxide or Ni-Mo, and designed so that the space velocity is such that the hydrogenated prod. stream (F) is practically olefin-free or ultimately contains below 0.3 wt.% olefins, the life-time of the catalyst being at least a year and at the same time S cpds. e.g. COS, being hydrogenated to sulphydric acid (e) passing a portion of hydrogenated gas, stream (G), through a ZnO fixed bed reactor to remove as ZnS the sulphydric acid in the refinery gas or produced is (d) followed by injection of the hydrogenated and S-free refinery gas, stream (K), in the water stream reformer (f) returning a portion of hydrogenated gas, stream (H), to heat exchanger, cooling the gas, stream (I), with water up to 140-170 (150) deg. C, sepg. liq. formed followed by injection of - gas, stream (I), in intermediate stage of compressor. (First major country equivalent to PT--81622-A)
机译:PT--81622一种方法包括(a)sepg。液体来自精炼厂气流(A)的物流,无液化气流分为供入燃气系统的物流(B)和组成氨厂原料(b)的物流(C)通过物流C压缩机吸气鼓并压缩,从而引起饱和的中间吸气。冷却的气体循环,将气体与进料混合,并从氢化反应器(c)中除去一部分反应生成的热量,从而以100-713 psi(7-50 kg / sq.cm)或更高的压力从(b)压缩气体。压力为385-713 psi(27-50 kg / sq。cm),形成料流(D),压缩机接收具有高浓度的低密度气体。来自重瓦斯油裂解的H2和高含量的Ni(d)加热流产生的真空残渣,从循环中回收热量,从氢化反应器中流出,通过混合气。 (E)通过反应器的进料-再循环气体,进料-再循环气体的比例被控制为使温度为。的反应器保持在最小。在不降低加氢反应速率的情况下,在催化剂上沉积焦炭的含量达到最低水平,反应器装有钴-氧化钼或Ni-Mo的固定床催化剂,并设计成使空速使得氢化产物。物流(F)实际上不含烯烃或最终含有低于0.3重量%的烯烃,催化剂的寿命为至少一年,并且同时为S cpds。例如通过ZnO固定床反应器将一部分氢化气流,料流(G)加氢生成硫酸(e),以去除炼厂气中或生成的硫酸中的ZnS,然后将其注入d水流重整器(f)中的氢气和不含S的炼油厂气流(K),将一部分氢气(H)送回热交换器,冷却气流(I),直至水140-170(150)度C,隔膜液体在压缩机的中间阶段形成气流,然后注入气流(I)。 (相当于PT--81622-A的第一个主要国家/地区)GBAB- GB2183670 B过程包括(a)sepg。液体来自精炼厂气流(A)的物流,无液化气流分为供入燃气系统的物流(B)和组成氨厂原料(b)的物流(C)通过物流C压缩机吸气鼓并压缩,从而引起饱和的中间吸气。冷却的气体循环,将气体与进料混合,并从氢化反应器(c)中除去一部分反应生成的热量,从而以100-713 psi(7-50 kg / sq.cm)或更高的压力从(b)压缩气体。压力为385-713 psi(27-50 kg / sq。cm),形成料流(D),压缩机接收具有高浓度的低密度气体。来自重瓦斯油裂解的H2和高含量的Ni(d)加热流产生的真空残渣,从循环中回收热量,从氢化反应器中流出,通过混合气。 (E)通过反应器的进料-再循环气体,进料-再循环气体的比例被控制为使温度为。的反应器保持在最小。在不降低加氢反应速率的情况下,在催化剂上沉积焦炭的含量达到最低水平,反应器装有钴-氧化钼或Ni-Mo的固定床催化剂,并设计成使空速使得氢化产物。物流(F)实际上不含烯烃或最终含有低于0.3重量%的烯烃,催化剂的寿命为至少一年,并且同时为S cpds。例如通过ZnO固定床反应器将一部分氢化气流,料流(G)加氢生成硫酸(e),以去除炼厂气中或生成的硫酸中的ZnS,然后将其注入d水流重整器(f)中的氢气和不含S的炼油厂气流(K),将一部分氢气(H)送回热交换器,冷却气流(I),并用水冷却至140-170(150)度C,隔膜液体在压缩机的中间阶段形成,然后注入-气流(I)。 (相当于PT--81622-A的第一大国)

著录项

  • 公开/公告号ES549908A0

    专利类型

  • 公开/公告日1986-05-16

    原文格式PDF

  • 申请/专利号ES19850549908

  • 发明设计人

    申请日1985-12-13

  • 分类号C01B3/48;

  • 国家 ES

  • 入库时间 2022-08-22 07:37:46

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