Isobaric ammonia preparation technology taking gaseous hydrocarbon after autothermal reforming as raw material

A technology for autothermal reforming and gaseous hydrocarbons, which is applied in the field of synthetic ammonia, can solve the problems of low ammonia concentration at the outlet, large equipment investment, complicated operation, etc., and achieves the effects of high yield, reduced investment and operating cost, and simple process.

Active Publication Date: 2017-08-18
FUZHOU UNIV ASSET MANAGEMENT CO LTD +1
View PDF5 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] The technical problem solved by the present invention is to overcome the defects of the existing low-pressure ammonia synthesis process that the outlet ammonia concentration is low and fluctuates greatly, and on the other hand, to solve the equipment investment in the existing two-stage natural gas conversion process Large and cumbersome operation, and then provide an isopressed ammonia process that can increase and stabilize the ammonia yield and reduce the overall system equipment investment, using gaseous hydrocarbons after autothermal reforming as raw materials

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Isobaric ammonia preparation technology taking gaseous hydrocarbon after autothermal reforming as raw material
  • Isobaric ammonia preparation technology taking gaseous hydrocarbon after autothermal reforming as raw material

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0043] This embodiment provides a method for preparing the second ruthenium-based catalyst, comprising the steps of:

[0044] (1) Dissolve 20g of urea in 100g of water to form a nitrogen-containing solution, load the nitrogen-containing solution on magnesium-aluminum hydrotalcite with a magnesium-aluminum molar ratio of 0.6, heat and dry at 100°C, and Roasting in a nitrogen atmosphere at 190°C for 2 hours to obtain nitrogen-doped magnesium aluminum hydrotalcite, the doping amount of nitrogen element by mass is 5.5% of the mass of magnesium aluminum hydrotalcite;

[0045] (2) The above-mentioned nitrogen-doped magnesium aluminum hydrotalcite was heated to 630°C at a rate of 15°C / min and kept roasted for 1h, and then heated to 700°C at a rate of 3°C / min and kept roasted for 0.75h, and the roasted product It is the catalyst carrier, which contains 30v% spinel phase;

[0046] (3) Heating potassium fluorotantalate and sulfuric acid to above 400°C, and then diluting with water to u...

Embodiment 2

[0050] This embodiment provides a method for preparing the second ruthenium-based catalyst, comprising the steps of:

[0051] (1) Dissolve 15ml of ammonia water in 90ml of water to form a nitrogen-containing solution, and load the nitrogen-containing solution on magnesium-aluminum hydrotalcite with a magnesium-aluminum molar ratio of 1.7 by an equal-volume impregnation method, heat and dry at 80°C, and Roasting in an ammonia atmosphere at 200°C for 0.5h to obtain nitrogen-doped magnesium aluminum hydrotalcite, the doping amount of nitrogen element by mass is 8% of the mass of magnesium aluminum hydrotalcite;

[0052] (2) The above-mentioned nitrogen-doped magnesium aluminum hydrotalcite was heated to 600°C at a rate of 10°C / min and kept roasted for 3h, and then heated to 710°C at a rate of 5°C / min and kept roasted for 0.5h, and the roasted product It is the catalyst carrier, which contains 45v% spinel phase, and the pore radius distribution is in the range of 5-21nm;

[0053]...

Embodiment 3

[0057] This embodiment provides a method for preparing the second ruthenium-based catalyst, comprising the steps of:

[0058] (1) 12ml of hydrazine hydrate was dissolved in 100ml of water to form a nitrogenous solution, and the nitrogenous solution was loaded on magnesium-aluminum hydrotalcite with a magnesium-aluminum molar ratio of 2.5 by an equal-volume impregnation method, heated and dried at 90°C, and Roasting in an ammonia atmosphere at 200° C. for 1 h to obtain nitrogen-doped magnesium aluminum hydrotalcite, the doping amount of nitrogen element by mass is 10% of the mass of magnesium aluminum hydrotalcite;

[0059] (2) The above-mentioned nitrogen-doped magnesium aluminum hydrotalcite was heated to 650°C at a rate of 5°C / min and kept roasted for 2h, and then heated to 720°C at a rate of 1°C / min and kept roasted for 0.5h, and the roasted product It is the catalyst carrier, which contains 37v% spinel phase;

[0060] (3) Heating potassium fluorotantalate and sulfuric aci...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
radiusaaaaaaaaaa
Login to view more

Abstract

The invention provides an isobaric ammonia preparation technology taking gaseous hydrocarbon after autothermal reforming as a raw material. The technology allows gaseous hydrocarbon to generate autothermal reforming conversion in the presence of an oxidizing agent and steam, so that arrangement of a primary converter can be omitted; the pressure of prepared synthesis gas is approximate to the pressure of ammonia synthesis, so that a synthesis gas compressor is also omitted; the prepared synthesis gas is subjected to ammonia synthesis reactions under different technology conditions in the presence of a first ruthenium-base catalyst and a second ruthenium-base catalyst sequentially, so that a hydrogen-nitrogen conversion rate and an ammonia yield are greatly increased by matching of the sequential two-stage reactions; ammonia concentration in outlet gas reaches 20.5-22.8%; and the technology is high in yield and low in fluctuation, and has a good industrial application prospect.

Description

technical field [0001] The invention belongs to the technical field of ammonia synthesis, and in particular relates to an isopressed ammonia process using gaseous hydrocarbons after autothermal reforming as raw materials. Background technique [0002] Ammonia is an important inorganic chemical product. Since the German chemist Haber discovered in 1902 that nitrogen and hydrogen can be directly synthesized into ammonia under high temperature and pressure and the presence of a catalyst, the ammonia synthesis industry has gradually developed into a pillar industry of the national economy. At present, the large-scale ammonia synthesis technology that is widely used in industry is the step-up ammonia synthesis process with a synthesis pressure above 15 MPa. The advantages of this process are that the synthesis pressure is high, the energy consumption of unreacted products is small, and the separation of ammonia is convenient. Due to the low pressure of the raw material synthesis ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): C01C1/04C01B3/02
CPCY02P20/52C01C1/0411C01B3/025
Inventor 江莉龙林建新倪军林炳裕林科
Owner FUZHOU UNIV ASSET MANAGEMENT CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap