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Mild hydrofining of light virgin naphthas

机译:轻度初榨石脑油的轻度加氢精制

摘要

Light virgin naphthas (boiling range C1 to 430 DEG F.) are desulphurized by contact at 450 DEG to 750 DEG F. with not more than 30 SCF/Bbl. of hydrogen in the presence of a hydrofining catalyst, the hydrogen consumption rate being below 25 SCF/Bbl. The pressure may be 50 to 800 p.s.i.g. and the feed rate 1 to 10 V/V/Hr. The feed may be unstabilized or stabilized by removal of C3 and lighter fractions. The hydrogen may be pure hydrogen or it may contain up to 60 degrees of inert diluents and may be derived from other refinery processes, e.g. hydroforming. H2, H2S and C3- hydrocarbons may be removed from the product in a flash drum. Residual traces of H2S may be removed by caustic washing, e.g. with 2-5 wt. per cent of S0Be caustic alkali. Preheating of the hydrogen is not necessary but it may be mixed with the feed before the latter is preheated. Hydrofining catalysts mentioned are 5 to 15 wt. per cent molybdenum oxide and mixtures of cobalt oxides (2-6 wt. per cent) and molybdenum oxides (6-15 wt. per cent), both an activated alumina. They may be regenerated at 900-1100 DEG F. with an oxygen-containing gas. In an example a C1-300 DEG F. virgin naphtha was treated at 600 DEG F., 550 DEG F. and 500 DEG F. with 30 SCF of hydrogen per barrel of feed at 225 p.s.i.g. and a feed rate of 4 V/V/Hr. using 10-14 mesh cobalt molybdate on alumina. The hydrogen consumption was 12-15 SCF/bbl.
机译:轻度纯正石脑油(沸点范围C1至430°F)通过在450°F至750°F下与不超过30 SCF / Bbl的接触脱硫。在加氢精制催化剂的存在下,氢气的消耗量低于25 SCF / Bbl。压力可以是50至800p.s.i.g。进给速度为1至10 V / V / Hr。进料可能因除去C3和较轻的馏分而不稳定或稳定。氢可以是纯氢,或者可以包含至多60度的惰性稀释剂,并且可以衍生自其他精炼工艺,例如氢气。液压成型。可以在闪蒸罐中从产品中除去H2,H2S和C3-烃。残留的痕量H2S可以通过苛性碱洗涤去除,例如与2-5 wt。 S0Be为苛性碱。不需要对氢气进行预热,但可以在进料被预热之前将其与进料混合。提及的加氢精制催化剂为5至15重量%。 %的氧化钼和氧化钴(2-6wt%)和氧化钼(6-15wt%)的混合物,两者均为活性氧化铝。它们可以在900-1100°F下用含氧气体再生。在一个实施例中,在225p.s.i.g下,每桶进料用30SCF的氢气在600°F,550°F和500°F下处理C1-300°F的原始石脑油。进给速度为4 V / V / Hr。在氧化铝上使用10-14目钼酸钴。氢消耗为12-15SCF / bbl。

著录项

  • 公开/公告号GB815957A

    专利类型

  • 公开/公告日1959-07-01

    原文格式PDF

  • 申请/专利权人 ESSO RESEARCH AND ENGINEERING COMPANY;

    申请/专利号GB19570031156

  • 发明设计人

    申请日1957-10-04

  • 分类号C10G45/02;

  • 国家 GB

  • 入库时间 2022-08-23 19:47:43

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