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Process for hydrogen sulfide removal from gas mixtures containing h2s and co2

机译:从含h2s和co2的气体混合物中去除硫化氢的方法

摘要

1,141,360. Recovery of sulphur. ALLIED CHEMICAL CORP. 25 Oct., 1966 [25 Oct., 1965; 15 Aug., 1966], No. 47901/66. Heading C1A. [Also in Divisions B1 and C5] H 2 S is removed from gas mixtures, especially from natural gas, by absorption at 1-105 kg/cm.SP2/SP, preferably up to 70 kg./cm.SP2/SP, in a liquid dialkyl ether of a polyalkylene glycol, which is subsequently regenerated by stripping at reduced pressure with an oxygen-containing gas such as air. The mixed gas stream of H 2 S and air is then preferably passed to a bauxite catalyst bed at 150-425‹ C. where the HS 2 is oxidized to sulphur, the effluent vapours from the bed being condensed to recover the sulphur in liquid or solid form. The solvent may be flashed at an intermediate pressure before stripping in order to remove absorbed gases other than H 2 S. The solvents generally contain 2-7 ethenoxy units, the dimethyl ether of tetraethylene glycol being preferred. In Fig. 2, natural gas having an H 2 S/CO 2 molar ratio of 0À1-10 enters sorber 2 by line 1 and sorbent by line 4, the pressure being maintained at 10À5-105 kg./cm.SP2/SP and the gas and liquid flow rates being so chosen that relatively little CO 2 is sorbed. Purified gas leaves at 5, charged solvent at a temperature of 0À5-44‹ C. passing by line 6 to be flashed to 1À05-35 kg./cm.SP2/SP in tank 7. The overhead, which comprises process gas and CO 2 , is returned by line 8 to sorber 2 while the solvent is heated in exchangers 10 and 11 on its way to stripping column 12 which is at 0À14-1À26 kg./cm.SP2/SP Air is fed in at the base and the effluent stream containing desorbed H 2 S passes to condenser 15, condensed solvent being returned to the stripper by line 16. Regenerated solvent is cooled in heat exchanger 10 and cooler 19 before being returned to the sorber. A process in which the stream of solvent is used first to remove and recover CO 2 from a gas stream from which the H 2 S has already been removed, and then, after flashing to remove the H 2 S from an incoming gas stream, is also described (see Fig. 3, not shown). In Fig. 1 (not shown), the effluent gas stream of H 2 S and air is passed by line (59) through heater (61), where more air enters by line (60), to bauxite catalyst bed (63), the effluent vapours being liquified in condenser (20) and molten sulphur recovered through line (21).
机译:1,141,360。回收硫。联合化学公司,1966年10月25日[1965年10月25日; 1966年8月15日],第47901/66号。标题C1A。 [也在B1和C5分区中]通过以1-105 kg / cm。 2 的吸收,从气体混合物,特别是从天然气中除去H 2 S,优选最高至70kg./cm。在聚亚烷基二醇的液态二烷基醚中的 2 ,随后通过在减压下用含氧气体(例如空气)汽提来再生。然后,最好将H 2 S和空气的混合气流送入150-425°C的铝土矿催化剂床中,在这里将HS 2氧化成硫,床中的流出蒸汽被冷凝以回收液体或水中的硫。固体形式。为了除去H 2 S以外的吸收气体,可以在汽提之前在中等压力下将溶剂闪蒸。溶剂通常包含2-7个乙氧基单元,四乙二醇的二甲醚是优选的。在图2中,H 2 S / CO 2摩尔比为0‑1-10的天然气通过管线1进入吸附器2,并通过管线4进入吸附剂,压力保持在10‑5-105 kg./cm.2 ,并且选择气体和液体的流速,以便吸收相对较少的CO 2。净化后的气体在5处离开,带电的溶剂在0‑5-44 ‹C的温度下通过管线6进入罐7中,闪蒸至1‑05-35 kg./cm。 2 。包含工艺气体和CO 2的气体经管线8返回吸附器2,同时在交换器10和11中将溶剂加热到吸附塔2的过程中,其流速为0‑14-1‑26 kg./cm.2空气从底部进入,含有脱附的H 2 S的流出物流进入冷凝器15,冷凝的溶剂通过管线16返回汽提塔。再生的溶剂先在热交换器10和冷却器19中冷却,然后再返回吸附器。 。首先使用溶剂流从已除去H 2 S的气流中除去和回收CO 2,然后在闪蒸以从进入的气流中除去H 2 S的过程是也进行了描述(见图3,未显示)。在图1(未显示)中,H 2 S和空气的流出气流通过管线(59)穿过加热器(61),然后更多的空气通过管线(60)进入铝土矿催化剂床(63),废气在冷凝器(20)中液化,熔融硫通过管线(21)回收。

著录项

  • 公开/公告号US3362133A

    专利类型

  • 公开/公告日1968-01-09

    原文格式PDF

  • 申请/专利权人 ALLIED CHEMICAL CORPORATION;

    申请/专利号US19660572460

  • 发明设计人 KUTSHER GEORGE S.;JR. GLENN A. SMITH;

    申请日1966-08-15

  • 分类号B01D53/52;C01B17/04;C10K1/16;

  • 国家 US

  • 入库时间 2022-08-23 12:57:37

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