Method for preparing liquid product containing rich phenols and alcohols through microwave catalytic thermal cracking of forestry and agricultural residues

A technology of microwave catalysis of agricultural and forestry wastes, which is applied in the field of alcohol liquid products and microwave catalytic pyrolysis of agricultural and forestry wastes to prepare rich phenols, which can solve the problems of low yield of pyrolysis liquid, non-enrichment of effective components, and heat dissipation Serious problems, to achieve the effect of improving thermal cracking efficiency, promoting rapid carbonization, and not easy to coke

Active Publication Date: 2017-05-10
SHAANXI UNIV OF SCI & TECH
View PDF7 Cites 16 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the traditional pyrolysis method mainly uses quartz sand or ceramic balls as bed materials to indirectly transfer heat to agricultural and forestry waste particles, resulting in uneven heat transfer, serious heat dissipation, low yield of pyrolysis liquid, and effective composition. problems such as enrichment

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
  • Method for preparing liquid product containing rich phenols and alcohols through microwave catalytic thermal cracking of forestry and agricultural residues
  • Method for preparing liquid product containing rich phenols and alcohols through microwave catalytic thermal cracking of forestry and agricultural residues
  • Method for preparing liquid product containing rich phenols and alcohols through microwave catalytic thermal cracking of forestry and agricultural residues

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0039] Be that the larch sawdust (moisture content 10%) of 0.1mm~0.45mm with particle diameter, the industrial silicon carbide that particle diameter is 10 μm~100 μm is an example to introduce the implementation process of the present invention as follows:

[0040] React 1 mole of industrial silicon carbide particles with 5 moles of chlorine gas at 1000°C for 2 hours to obtain modified silicon carbide. Dissolve 10g of nickel nitrate in 50g of absolute ethanol, then add 10g of modified silicon carbide, stir continuously for 30 minutes, seal and let stand for 12 hours, evaporate to dryness in a water bath at 50°C, and then place the evaporated solid in Calcining at 600° C. for 6 hours under an air atmosphere to obtain a nickel oxide supported catalyst. Dissolve 10g of palladium chloride in 50g of absolute ethanol, then add 10g of modified silicon carbide, stir continuously for 30 minutes, seal and let stand for 12 hours, evaporate the absolute ethanol to dryness in a 50°C water ...

Embodiment 2

[0042] Be that the corn stalk (moisture content 8%) of 0.45mm~0.9mm with particle diameter, the nano-silicon carbide that particle diameter is 100 μm~200 μm is an example to introduce the implementation process of the present invention as follows:

[0043] React 1 mole of nano-silicon carbide with 0.2 mole of hydrogen fluoride at 1200° C. for 1.5 hours to obtain modified silicon carbide. Dissolve 10g of ferric nitrate in 50g of absolute ethanol, then add 12g of modified silicon carbide, stir continuously for 45 minutes, seal and let stand for 20 hours, evaporate to dryness in a water bath at 55°C, and then place the evaporated solid in Calcining at 650° C. for 4 hours under an air atmosphere to obtain an iron oxide-supported catalyst. Dissolve 10g of ruthenium chloride in 50g of absolute ethanol, then add 12g of modified silicon carbide, stir continuously for 40 minutes, seal and let stand for 15 hours, evaporate the absolute ethanol to dryness in a 70°C water bath, and then d...

Embodiment 3

[0045] Be that 0.9mm~1.2mm wheat straw (moisture content 6%), particle diameter be 250 μ m~350 μ m α-silicon carbide as an example to introduce the implementation process of the present invention as follows with particle diameter:

[0046] 1 mole of α-silicon carbide was reacted with 3 moles of ammonium bromide at 1800° C. for 0.5 hour to obtain modified silicon carbide. Dissolve 10g of calcium nitrate in 50g of absolute ethanol, then add 50g of modified silicon carbide, stir continuously for 60 minutes, seal and let stand for 24 hours, evaporate to dryness in a water bath at 70°C, and then place the evaporated solid in Calcined at 800° C. for 3.5 hours in an air atmosphere to obtain a calcium oxide-supported catalyst. Dissolve 10g of rhodium chloride in 50g of absolute ethanol, then add 50g of modified silicon carbide, stir continuously for 60 minutes, seal and let stand for 24 hours, evaporate the absolute ethanol to dryness in a 70°C water bath, and then evaporate the evapo...

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
particle diameteraaaaaaaaaa
particle diameteraaaaaaaaaa
particle diameteraaaaaaaaaa
Login to view more

Abstract

The invention discloses a method for preparing a liquid product containing rich phenols and alcohols through microwave catalytic thermal cracking of forestry and agricultural residues and belongs to the technical field of biomass energy. The method is a new method for obtaining the liquid product containing rich phenols and alcohols by organically combining microwave absorbent silicon carbide with a catalytic active metal component and through primary solid-phase microwave catalytic thermal cracking and secondary gas-phase cracking reaction, and resourceful conversion and high-value utilization of the forestry and agricultural residues are promoted.

Description

technical field [0001] The invention belongs to the technical field of biomass energy, and in particular relates to a method for preparing liquid products rich in phenols and alcohols by microwave catalytic pyrolysis of agricultural and forestry wastes. Background technique [0002] Agricultural and forestry waste is an important biomass resource, mainly including crop straw, rice husk, wood harvesting residue, wood processing residue, etc. Its energy conversion and utilization is one of the research hotspots in the field of renewable energy. Pyrolysis liquefaction technology can convert agricultural and forestry waste into pyrolysis oil, pyrolysis charcoal and pyrolysis gas, which is an important conversion method for resource utilization of agricultural and forestry waste. However, the traditional pyrolysis method mainly uses quartz sand or ceramic balls as bed materials to indirectly transfer heat to agricultural and forestry waste particles, resulting in uneven heat tran...

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): C10G1/00B01J27/224B01J19/12
CPCB01J19/126B01J27/224C10G1/00C10G2300/1014C10G2300/70
Inventor 王文亮李新平韩卿薛白亮侯青青
Owner SHAANXI UNIV OF SCI & TECH
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