Catalyst system for ethylene oligomerization as well as preparation method and application thereof

A technology of ethylene oligomerization and catalyst, applied in the direction of catalyst, carbon compound catalyst, chemical instrument and method, etc., can solve problems such as no report

Pending Publication Date: 2021-03-12
XLINK TECH CO LTD HANGZHOU
View PDF19 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, for the coproduction of ethylene trimerization and tetramerization, there are currently no reports

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
  • Catalyst system for ethylene oligomerization as well as preparation method and application thereof
  • Catalyst system for ethylene oligomerization as well as preparation method and application thereof
  • Catalyst system for ethylene oligomerization as well as preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0054] 1. Synthesis of perfluoronaphthyl PNP ligand

[0055] 1.1, the preparation of 2-bromoheptafluoronaphthalene

[0056]

[0057] Dissolve 25g of octafluoronaphthalene in 150mL of ethanol, stir and heat up to reflux, add 10g of hydrazine hydrate dropwise within 30min, continue to heat and reflux for 4 hours after the dropwise addition, evaporate ethanol at normal pressure, add 200mL of water to the residue, stir and cool to room temperature, The solid was collected by filtration.

[0058] The above solid was added to a mixture of 150mL hydrobromic acid and 20g copper bromide, stirred and heated to reflux for 6 hours, cooled to room temperature, the reaction mixture was extracted three times with 80mL ethyl acetate, the combined organic layers were washed with water, dried, and desolvated, and the obtained solid was used for Methanol was recrystallized to obtain 18 g of yellow solid.

[0059] 1.2. Preparation of PNP ligand

[0060]

[0061] Dissolve 18 g of 2-bromoh...

Embodiment 2

[0073] 1. Synthesis of 5-quinolinyl PNP ligand

[0074] 1.1, Preparation of 5-bromoquinoline

[0075]

[0076] Dissolve 15g of quinoline in 300mL of dichloromethane, add 35g of NBS under stirring at room temperature, and react at room temperature until the reaction of the raw materials is complete, stop the reaction, wash with saturated saline, dry and remove the solvent, and separate by column chromatography to obtain 10.4g of light yellow solid .

[0077] 1.2. Preparation of PNP ligand

[0078]

[0079]Dissolve 10.4 g of 5-bromoquinoline in 50 mL of ether, and add the solution dropwise at room temperature to a suspension of 50 mL of ether containing 1.4 g of magnesium chips, keep stirring, and control the reaction until the magnesium chips disappear completely; 3.4g of phosphorus trichloride was added dropwise to the above mixture at 0°C, then raised to room temperature and stirred for 1 hour, filtered to remove the magnesium salt under the protection of argon, and t...

Embodiment 3

[0090] 1, Synthesis of 6-halazinyl PNP ligand

[0091] 1.1, Preparation of 6-bromothazine

[0092]

[0093] Stir and cool the tetrahydrofuran suspension (350mL) containing 8.2g lithium aluminum hydride to -78°C, slowly add 200mL tetrahydrofuran solution containing 27g 4-bromophthalic acid dropwise within 2 hours, and raise the temperature within 2 hours after the dropwise addition to room temperature, and then heated to reflux for 2 hours. Subsequently, the mixture was cooled to 0°C, and 100 mL of 15% sodium hydroxide solution was slowly added dropwise, vacuum filtered, the filter residue was washed with 200 mL of water and 200 mL of tetrahydrofuran, respectively, the filtrate and washings were combined, and extracted with diethyl ether (100 mL×3), The oil layers were combined, washed with brine, dried and precipitated to obtain 16.4 g of 4-bromo-phthalamide as a white solid.

[0094] The mixed solution of 15mL oxalyl chloride and 180mL dichloromethane was stirred and coo...

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 discloses a novel catalyst system with high activity and high selectivity for ethylene oligomerization as well as a preparation method and application thereof. The catalyst system comprises a novel PNP ligand, a transition metal compound and a cocatalyst. According to the PNP ligand, a binary ring-fused aromatic group is used for replacing a phenyl group in a conventional PNP ligand,and a binary ring-fused aromatic substituent has more substitution positions, richer aromatic ring electron cloud distribution modes and larger space volume than a benzene ring, so more and strongerinfluences can be provided for a donor part of the ligand; and therefore, the catalyst shows more excellent linear alpha-olefin (LAO) selectivity in an ethylene oligomerization reaction, and 1-hexeneor 1-octene can be prepared with high selectivity.

Description

technical field [0001] The invention belongs to the field of industrial catalysts, and relates to an ethylene oligomerization catalyst system and its preparation method and application, in particular to an ethylene selective oligomerization catalyst system and a method for preparing 1-hexene and / or 1-octene through the catalyst system . Background technique [0002] Linear alpha-olefins refer to C with double bonds at the ends of the molecule 4 And above linear olefins are a kind of important petrochemical raw materials with wide application. Among them, high-grade α-olefins such as 1-hexene and 1-octene can not only be used to prepare high-end polyolefin materials, but also can be used in high-grade detergents, high-grade alcohols, high-performance PAO lubricants, surfactants and oil additives, etc. The production of important products has a huge market demand. However, the domestic output of 1-hexene, 1-octene and other high-grade α-olefins is still small, especially 1-...

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
IPC IPC(8): B01J31/22C07F9/60C07F9/6509C07F9/6541C07F9/46C07C2/32C07C11/02C07C11/107
CPCB01J31/188C07F9/60C07F9/6509C07F9/6541C07F9/46C07C2/32B01J2231/20B01J2531/62C07C2531/22B01J2531/0255C07C11/02C07C11/107Y02P20/52
Inventor 魏东初柳庆先叶健
Owner XLINK TECH CO LTD HANGZHOU
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