A method for preparing high-content aromatic hydrocarbon products from oily sludge
A technology with high content of aromatic hydrocarbons, applied in chemical instruments and methods, preparation of liquid hydrocarbon mixtures, and treatment of hydrocarbon oils, etc., can solve the problems of low yield of aromatic hydrocarbons and large consumption of fossil fuels, and achieve simple preparation process and low cost Low, High Feasibility Effects
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0029] 5.48g Zn(NO 3 ) 2 ·6H 2 The aqueous solution of O solid was added dropwise to 40 g of conventional ZSM-5 molecular sieve powder obtained after vacuum degassing for 1 hour, impregnated at room temperature for 12 hours, and then rotary evaporated under vacuum and 60 ° C water bath conditions for 1 hour, and then heated at 110 ° C Bake for 12 hours, and then calcined at 550°C for 5 hours in air atmosphere. After natural cooling, a massive solid is obtained, which is ground into 100-200 mesh (0.074-0.150mm) powder to obtain a molecular sieve catalyst with a zinc loading of 3%. After uniformly mixing 6g of the obtained zinc-loaded molecular sieve powder with 6g of quartz sand, put it into the second section of the tube furnace to ensure that the length of the catalytic section is 90mm, and then raise the temperature of the second section to 500°C and keep it warm. Put 1.5g of oily sludge in a porcelain boat, put it into the first section of the tube furnace, and raise the ...
Embodiment 2
[0035] 5.48g Zn(NO 3 ) 2 ·6H 2The aqueous solution of O solid was added dropwise to 20 g of conventional ZSM-5 molecular sieve powder obtained after vacuum degassing for 1 hour, impregnated at room temperature for 12 hours, and then rotary evaporated under vacuum and 60 ° C water bath conditions for 1 hour, and then heated at 110 ° C Bake for 12 hours, and then calcined at 550°C for 5 hours in air atmosphere. After natural cooling, a massive solid is obtained, which is ground into 100-200 mesh (0.074-0.150mm) powder to obtain a molecular sieve catalyst with a zinc loading of 6%. After uniformly mixing 6g of the obtained zinc-loaded molecular sieve powder with 6g of quartz sand, put it into the second section of the tube furnace to ensure that the length of the catalytic section is 90mm, and then raise the temperature of the second section to 500°C and keep it warm. Put 1.5g of oily sludge in a porcelain boat, put it into the first section of the tube furnace, and raise the t...
Embodiment 3
[0037] 5.48g Zn(NO 3 ) 2 ·6H 2 The aqueous solution of O solid was added dropwise to 40 g of conventional ZSM-5 molecular sieve powder obtained after vacuum degassing for 1 hour, impregnated at room temperature for 12 hours, and then rotary evaporated under vacuum and 60 ° C water bath conditions for 1 hour, and then heated at 110 ° C Bake for 12 hours, and then calcined at 550°C for 5 hours in air atmosphere. After natural cooling, a massive solid is obtained, which is ground into 100-200 mesh (0.074-0.150mm) powder to obtain a molecular sieve catalyst with a zinc loading of 3%. After uniformly mixing 6g of the obtained zinc-loaded molecular sieve powder with 6g of quartz sand, put it into the second section of the tube furnace to ensure that the length of the catalytic section is 90mm, and then raise the temperature of the second section to 500°C and keep it warm. Put 1.5g of oily sludge in a porcelain boat, put it into the first section of the tube furnace, and raise the ...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More - R&D
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com



