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Skeletal iron catalyst and its preparation for fischer-tropsch synthesis processes

a technology of skeletal iron and catalyst, which is applied in the field of skeletal iron catalysts, can solve the problems of inconvenient preparation of precipitated iron catalyst, and inability to meet the requirements of the application of the catalyst, and achieves significant selectivity and stable activity.

Inactive Publication Date: 2002-01-24
ZHOU JINGLAI +7
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0004] The resulting skeletal iron catalyst has high activity and provides good selectivity towards the formation of desirable low-molecular-weight hydrocarbon products from the CO and H.sub.2 feedstreams. This catalyst has catalytic activity equivalent to that of precipitated iron catalyst and product selectivity exceeding that of either precipitated or fused iron catalysts,and can be utilized in either fixed bed or slurry bed type reactors for Fischer-Tropsch synthesis reaction processes.
[0006] (a) The preparation method and pretreatment procedures for skeletal iron catalyst are relatively simple and inexpensive.
[0009] (d) For slurry-phase Fischer-Tropsch synthesis processes, the skeletal iron catalyst has stable activity and significant selectivity for low molecular weight hydrocarbons (C.sub.4 selectivity>10%).

Problems solved by technology

However, the preparation procedure for the precipitated iron catalyst is undesirably complicated and includes several steps of precipitation, washing, filtration, drying, formation, calcination, pulverization, and reduction.
Also, the precipitated iron catalyst is significantly influenced by various parameters, including precipitating agent, solution concentration, precipitation temperature, solution pH value, pretreatment temperature, and atmosphere, and such catalyst is undesirably expensive.
Furthermore, the fused iron catalyst has undesirably low active surface area (.about.10 m.sup.2 / g) that is difficult to increase, and it also has low catalytic activity and minimal economic advantage.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

example i

[0019] 1. Add metal iron and aluminum powders together with small amount of copper oxide promoter in weight ratio 49:50:1 into an electric-arc induction furnace, evacuate the air and fill the furnace with argon inert blanketing gas, then apply 450 A, 25 V electric current to induce an electric arc for heating and melting the powder materials uniformly during magnetic stirring. Then cool the iron-aluminum alloy material to room temperature and mechanically pulverize the alloy material to 0.1-1 mm particle size to produce metal alloy precursor material particles.

[0020] 2. Under hydrogen atmosphere, add a volume of 25% concentration NaOH in a stirred container, heat to temperature of 85.degree. C., then add the precursor iron alloy particles into the caustic solution at certain time intervals, and maintain reaction condition for 30 minutes to dissolve or extract the aluminum from the iron particles. Then wash the particles with deionized water to pH=7, displace water with water-free et...

example ii

[0023] 1. Add metal iron and aluminum power and a small amount of copper oxide at weight proportion of 25:74:1 into an electric-arc induction furnace, evacuate the air, and fill with argon gas for protection. Use 450 A, 25 V electric current to ignite electric arc for heating and melting the metal powders uniformly during magnetic stirring. Then quench the molten iron-aluminum alloy to room temperature, and mechanically pulverize the metal alloy material to 0.1-1 mm particle size to provide precursory metal particles. Steps 2, 3 and 4 were the same as for Example I.

example iii

[0024] Add metal iron and aluminum powder and a small amount of copper oxide promoter at weight ratios of 33:66:1 in an electric-arc induction furnace, evacuate the air, and fill with argon gas for protection. Use 450 A, 25 V current to ignite electric arc to heat the metal powders and melt uniformly during magnetic stirring. Then cool metal alloy to room temperature, and mechanically pulverize to 0.1-1 mm precursor particles. Steps 2, 3, and 4 were the same as for Example I.

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Abstract

Skeletal iron catalysts are prepared and utilized for producing synthetic hydrocarbon products from CO and H2 feeds by Fischer-Tropsch synthesis process. Iron powder is mixed with aluminum, antimony, silicon, tin or zinc powder and 0.01-5 wt. % metal promotor powder to provide 20-80 wt. % iron content, then melted together, cooled to room temperature and pulverized to provide 0.1-10 mm iron alloy catalyst precursor particles. The iron alloy precursor particles are treated with NaOH or KOH caustic solution at 30-95° C. to extract or leach out a major portion of the non-ferrous metal portion from the iron and provide the skeletal iron catalyst material. Such skeletal iron catalyst is utilized with CO+H2 feedstream in either fixed bed or slurry bed type reactor at 200-350° C. temperature, 1.0-3.0 mPa pressure and gas hourly space velocity of 0.5-3.0 L / g Fe / h to produce desired hydrocarbon products.

Description

BACKGROUND OF INVENTION[0001] This invention pertains to skeletal iron catalysts, and particularly pertains to catalyst preparation methods and process for use of such catalysts in Fischer-Tropsch synthesis processes for CO and H.sub.2 feeds to produce hydrocarbon products.[0002] As a basic technology for producing synthetic liquid fuels from CO+H.sub.2 feedstreams, the Fischer-Tropsch catalytic synthesis process has undergone worldwide development and use since the 1920s. Iron-based catalysts have been widely investigated and used and precipitated iron catalyst and fused iron catalyst have been the commonly used catalysts in such F-T synthesis processes. However, the preparation procedure for the precipitated iron catalyst is undesirably complicated and includes several steps of precipitation, washing, filtration, drying, formation, calcination, pulverization, and reduction. Also, the precipitated iron catalyst is significantly influenced by various parameters, including precipitat...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): B01J23/745B01J25/00B01J37/00B01J37/06B22F9/16C07C1/04C10G2/00C22C38/06C22C38/16
CPCB01J23/745B01J25/00B01J37/0018B01J37/0036B01J37/06B22F9/16C07C1/0445C07C1/046C07C2521/02C07C2521/06C07C2523/06C07C2523/14C07C2523/745C07C2523/78C07C2523/843C10G2/332C22C38/06C22C38/16
Inventor ZHOU, JINGLAILU, YIJUNZHANG, ZHIXINLI, GUOHUIDONG, LINYAOWANG, HAIRONGZHOU, PEIZHENGLEE, LAP-KEUNG
Owner ZHOU JINGLAI
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