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A copper-cobalt-based catalyst for hydrolytic removal of organic sulfur and its preparation method

A catalyst and organic sulfur technology, applied in the field of copper-cobalt-based catalysts and their preparation, can solve the problems of easy loss of active alkali metal species, catalyst deactivation, etc., achieve high-efficiency catalytic hydrolysis performance, high raw material utilization, reduce environmental protection and production cost effect

Active Publication Date: 2021-09-28
中琉科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, these catalysts have problems such as easy loss of active alkali metal species under high water vapor concentration, which leads to catalyst deactivation.

Method used

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  • A copper-cobalt-based catalyst for hydrolytic removal of organic sulfur and its preparation method
  • A copper-cobalt-based catalyst for hydrolytic removal of organic sulfur and its preparation method
  • A copper-cobalt-based catalyst for hydrolytic removal of organic sulfur and its preparation method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0025] Add 0.0305g (0.13mmol) copper nitrate trihydrate and 3.6378g (12.50mmol) cobalt nitrate hexahydrate to 80mL ethylene glycol, stir at 300r / min for 1 hour until completely dissolved, then add 1.1g (27.5mmol) to the solution ) sodium hydroxide, after stirring vigorously at 600r / min for 1 hour, add 0.5g polyvinylpyrrolidone (PVP) and 0.5g oxalic acid and stir thoroughly for 1 hour, transfer the mixed solution to a polytetrafluoroethylene lining, and place under high pressure Reacted at 180°C for 18 hours in a kettle reactor. After the reaction is finished, cool to room temperature, then use ethanol and deionized water to centrifuge and wash until the pH of the supernatant is neutral, then dry the precipitate in an oven at 80-100°C for 12 hours to constant weight, and after grinding, you will get The solid powder was calcined at 350°C for 3 hours in an air atmosphere, then mechanically pressed into tablets, and sieved (40-60 mesh) to obtain Cu / Co 3 o 4 Catalyst, denoted as...

Embodiment 2

[0027] Add 0.1589g (0.66mmol) copper nitrate trihydrate and 3.6378g (12.50mmol) cobalt nitrate hexahydrate to 80mL ethylene glycol, stir the solution at 300r / min for 1 hour until completely dissolved, then add 1.1g (27.5 mmol) sodium hydroxide, after stirring vigorously at 600r / min for 1 hour, add 0.5g polyvinylpyrrolidone (PVP) and 0.5g oxalic acid and stir thoroughly for 1 hour, transfer the mixed solution to a polytetrafluoroethylene lining, place In an autoclave reaction device, the reaction was carried out at 180° C. for 18 hours. After the reaction is finished, cool to room temperature, then use ethanol and deionized water to centrifuge and wash until the pH of the supernatant is neutral, then dry the precipitate in an oven at 80-100°C for 12 hours to constant weight, and after grinding, you will get The solid powder was calcined at 350°C for 3 hours in an air atmosphere, then mechanically pressed into tablets, and sieved (40-60 mesh) to obtain Cu / Co 3 o 4 Catalyst, de...

Embodiment 3

[0029] Add 0.2626g (1.09mmol) copper nitrate trihydrate and 3.6378g (12.50mmol) cobalt nitrate hexahydrate to 80mL ethylene glycol, stir at 300r / min for 1 hour until completely dissolved, then add 1.1g (27.5mmol) to the solution ) sodium hydroxide, after stirring vigorously at 600r / min for 1 hour, add 0.5g polyvinylpyrrolidone (PVP) and 0.5g oxalic acid and stir thoroughly for 1 hour, transfer the mixed solution to a polytetrafluoroethylene lining, and place under high pressure Reacted at 180°C for 18 hours in a kettle reactor. After the reaction is finished, cool to room temperature, then use ethanol and deionized water to centrifuge and wash until the pH of the supernatant is neutral, then dry the precipitate in an oven at 80-100°C for 12 hours to constant weight, and after grinding, you will get The solid powder was calcined at 350°C for 3 hours in an air atmosphere, then mechanically pressed into tablets, and sieved (40-60 mesh) to obtain Cu / Co 3 o 4 Catalyst, denoted as...

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Abstract

The invention discloses a copper-cobalt-based catalyst for hydrolytic removal of organic sulfur and a preparation method thereof. The copper-doped tricobalt tetroxide catalyst is prepared by using a hydrothermal assisted co-precipitation synthesis method combined with high-temperature roasting. The copper-cobalt-based catalyst prepared by the invention exhibits high crystallinity, nano flake shape, mesoporous dominance, high ion diffusion rate, and high-efficiency catalytic hydrolysis performance for carbonyl sulfide. When the reaction temperature is 70°C, the conversion rate of COS is as high as 100%, which is suitable for low-temperature catalytic hydrolysis desulfurization of carbonyl sulfide-containing gases such as blast furnace gas and natural gas.

Description

technical field [0001] The invention belongs to the technical field of gaseous sulfide removal, and in particular relates to a copper-cobalt-based catalyst capable of hydrolyzing and removing organic sulfur at low temperature and a preparation method thereof. Background technique [0002] Gaseous sulfur-containing compounds are often present in blast furnace gas, oil, water gas and natural gas, causing equipment corrosion and catalyst poisoning and deactivation, resulting in a decrease in the quality of chemical products in subsequent chemical processes and causing damage to the environment. Among them, carbonyl sulfide gas (COS) is one of the most difficult sulfur-containing gases to remove due to its chemical stability, and it is also one of the main sources of sulfate aerosols in the atmosphere. In view of increasingly stringent environmental regulations and catalytic technical specifications, the removal of COS is urgent. COS can be removed by high-temperature catalytic...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): B01J23/75B01D53/48B01D53/86
CPCB01D53/485B01D53/8606B01J23/75
Inventor 江莉龙穆冠羽梁诗景曹彦宁郑勇刘福建
Owner 中琉科技有限公司