Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

The method for producing n-propylbenzene from benzene and isopropanol

A technology of isopropanol and n-propyl benzene, applied in the field of producing n-propyl benzene, can solve problems such as cumbersome reaction steps, unsuitable for industrial production, etc., and achieve the effects of simple technological process, low production cost, and avoidance of rearrangement

Active Publication Date: 2021-06-22
CHINA PETROLEUM & CHEM CORP +1
View PDF5 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This reaction step is loaded down with trivial details not suitable for industrial production

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
  • The method for producing n-propylbenzene from benzene and isopropanol
  • The method for producing n-propylbenzene from benzene and isopropanol
  • The method for producing n-propylbenzene from benzene and isopropanol

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0018] Synthesis of ZSM-5 molecular sieves with MFI topology.

[0019] First prepare colloidal seeds, 710.3g H 2 O, 13.8g NaOH and 117.0g TPAOH (20% solution) solution are fully dissolved and mixed until uniform, and then 158.9g silicic acid is gradually added to the above solution under stirring, fully shaken at room temperature for 1h, and aged at 100°C 16h; 867.8g H 2 O, 8.8g NaOH and 10.3g sodium aluminate are fully mixed and dissolved, 113.1g silicic acid is gradually added to the above mixed solution under full stirring and shaken violently for 1h, and 50g of the prepared colloidal seed crystals are added to the above mixed solution Shake for 1 h, then transfer the material to a stainless steel reactor. After crystallization at 180°C for 40h, the crystalline product was filtered, washed and dried. The crystalline product obtained by XRD powder diffraction analysis is ZSM-5 molecular sieve, and its silicon-aluminum ratio is 12-13.5.

[0020] Take 50 g of dried powder ...

Embodiment 2

[0022] Synthesis of Y-type molecular sieves with FAU topology.

[0023] First prepare colloidal directing agent, 20.0g H 2 O, 4.0g NaOH and 2.1g sodium aluminate (20% solution) solution were fully dissolved and mixed until uniform, then 22.7g silicic acid was gradually added to the above solution under stirring, fully shaken at room temperature for 1h, and aged at room temperature overnight; 261.9g H 2 O, 0.28g NaOH and 20.6g sodium aluminate are fully mixed and dissolved, 284.8g silicic acid is gradually added to the above mixed solution under full stirring and shaken violently for 1h, and 50g of the prepared directing agent is added to the above mixed solution Shake in medium for 1h. The material was then transferred to a stainless steel reactor. After crystallization at 100°C for 10 h, the crystalline product was filtered, washed and dried. The crystalline product obtained by XRD powder diffraction analysis is Y-type molecular sieve.

[0024] Take 50 g of dried powder ...

Embodiment 3

[0026] Synthesis of Beta molecular sieves with BEA topology.

[0027] 600g 40wt.% silica sol, 38.9g sodium aluminate (alumina content 42wt.%), 70.6g 25wt.% tetraethylammonium hydroxide (TEAOH), 5.0g diethylamine (DEA), 168.0g tetraethyl Ammonium bromide (TEABr), 16.0g of sodium hydroxide, 136.0g of 25wt.% ammonium hydroxide, and 925.1g of water were mixed and stirred evenly at room temperature. Then transferred to a stainless steel autoclave, the crystallization temperature was 155°C, and reacted for 50 hours. After the reaction, the crystalline product was filtered, washed and dried. The crystalline product obtained by XRD powder diffraction analysis is Beta zeolite.

[0028] Take 50 g of dried powder sample, exchange 4 times with 1M ammonium nitrate, filter and dry. After that, fully mix with 20g alumina, and add 5wt% nitric acid to knead, extrude and form into The strips were dried at 120°C for 12 hours and calcined at 500°C for 6 hours to prepare the required cataly...

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

No PUM Login to View More

Abstract

The invention relates to a method for producing n-propylbenzene from benzene and isopropanol, comprising the step of contacting benzene and isopropanol with a catalyst under effective reaction conditions to obtain n-propylbenzene; it is characterized in that said effective reaction conditions include a temperature of at least Greater than 200°C. The method can be used in the industrial production of n-propylbenzene.

Description

technical field [0001] The invention relates to a method for producing n-propylbenzene from benzene and isopropanol. Background technique [0002] Propylbenzene is an important chemical product, which can be directly used as a solvent and an intermediate in the synthesis of other important chemical raw materials. There are two main isomers of propylbenzene, cumene and n-propylbenzene. Cumene is an important intermediate in the production of phenol, acetone and α-methylstyrene, and can also be used as an additive to increase the octane number of fuel oil, a raw material for synthetic fragrances and polymerization initiators, etc. N-propylbenzene can be used in textile dyes, printing, and acetate cellulose solvent. The latest use is to use it as a nucleating agent for synthesizing sorbitol-based polypropylene. The sorbitol nucleating agent is produced by aldol condensation reaction, and is synthesized by introducing propyl or allyl into the sorbitol molecule, and introducin...

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 Patents(China)
IPC IPC(8): C07C1/24C07C15/02B01J29/40B01J29/08B01J29/70B01J29/18
CPCB01J29/084B01J29/18B01J29/40B01J29/7007B01J29/7038C07C1/24C07C15/02
Inventor 王高伟高焕新魏一伦胥明尤陈佳顾瑞芳方华季树芳姚辉刘远林
Owner CHINA PETROLEUM & CHEM CORP
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

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

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com