A method for preparing high molecular compounds by adopting a novel ion liquid polymerization initiation system

A polymer compound and ionic liquid technology, which is applied in the field of preparation of polymer compounds by the ionic liquid polymerization initiation system, can solve the problems of difficult recycling of catalysts, large amount of catalysts, and high processing costs, so as to achieve a wide range of catalyst selection and avoid the influence of toxicity , the effect of avoiding pollution

Inactive Publication Date: 2009-03-04
HANGZHOU NORMAL UNIVERSITY
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] There are still defects in the current ATRP system: because the polymerization rate is related to the amount of catalyst and ligand, in order to achieve a suitable polymerization rate, the amount of catalyst in the polymerization system is relatively large (1:100); The bond strength is greater than the C-Br bond, so for the Cl-ATRP system, the polymerization temperature is generally 100-130°C; for the Br-ATRP system, the polymerization temperature is 80-110°C, and the polymerization temperature is also higher, thereby increasing the production cost. ;Use organic solvents as medium, which will pollute the environment; the toxicity of the added amine ligands; after the polymerization of small molecule ligand catalysts of transition metals, the catalysts need to be cumbersomely processed before they can be separated, and the processing costs are too high; difficult to recycle

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

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0022] Example 1. Atom transfer radical polymerization of methyl methacrylate (MMA) in methylimidazole formate ionic liquid ([mim][HCOO])

[0023] Weigh 1 part of CuBr (cuprous bromide, the same below) 3 parts of CuBr 2 (Copper bromide) was dissolved in 500 parts of [mim][HCOO] (methylimidazole formate, the same below) ionic liquid, and nitrogen was passed to remove oxygen. Weigh 500 parts of MMA (methyl methacrylate, the same below) monomer, pass nitrogen to remove oxygen, add to ionic liquid, continue to pass nitrogen to remove oxygen, seal, keep the temperature at 50°C for 20 minutes, inject 1 part of 2 -Ethyl bromoisobutyrate initiator, react at a constant temperature of 50°C. One hour later, the polymerization liquid was treated with methanol to obtain PMMA (polymethyl methacrylate, the same below), Mn=55514, PDI=1.34.

Embodiment 2

[0024] Example 2. Methylimidazole acetate ([mim][CH 3 Atom Transfer Radical Polymerization of Methyl Methacrylate (MMA) in COO]) Ionic Liquid

[0025] Weigh 1 part of CuBr, in 100 parts of [mim][CH 3 COO] dissolved in the ionic liquid, nitrogen in addition to oxygen. Weigh 100 parts of MMA monomer, add nitrogen to remove oxygen, add to ionic liquid, continue to pass nitrogen to remove oxygen, seal, keep the temperature at 50°C for 20 minutes, inject different proportions of initiators, and react at a constant temperature of 50°C. result:

[0026] reaction a t / min conversion rate / % b mn c Mw / Mn

[0027] 1d 210 62.62 28428 1.32

[0028] 2e 60 43.28 13653 1.17

[0029] 3f 60 60.21 9723 1.17

[0030] 4g 60 65.13 8583 1.22

[0031] 5h 60 72.61 8018 1.14

[0032] (In the above table, Mn is the number average molecular weight, Mw is the weight average molecular weight)

[0033] a. All reactions were carried out at a ratio of 100:100 of MMA:[mi...

Embodiment 3

[0037] Example 3. Polymethyl methacrylate (PMMA) in methylimidazole acetate [mim] [CH 3 COO] ionic liquid, repolymerization in cuprous bromide (CuBr) system

[0038] Weigh 1 part of CuBr, dissolve it in 100 parts of [mim][HCOO] ionic liquid, pass nitrogen to remove oxygen, and keep the temperature at 50°C for 20 minutes. Weigh 0.12 parts of PMMA (Mn=5968) and dissolve it in 100 parts of MMA monomer. After purging nitrogen to remove oxygen, keep the temperature at 50°C for 20 minutes, add it to the ionic liquid, seal it, and react at a constant temperature of 50°C. Result: PMMA with Mn=26533 was obtained.

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 which using new ionic liquor polymerization initiation systerm prepares macromolecular compound. The technical matters of this invention needs to settle is providing a bran-new initiation systerm of atom radical transfer free radical polymerization which using ionic liquor as polymerization medium. The characteristic of this invention's method is the polymerization initiation systerm made up of ionic liquor, initiator and catalysator; the general formula of initiation systerm is [mim][RCOO] / R1X / MXn, the [mim][RCOO] is methyl imidazole organic acid salt ionic liquor, R is alkyl group; R1X is initiator, R1 is alkyl, X is halogen; catalysator MXn is transient metal inorganic salt, n is valence number equal to transition metal; initiation systerm reacts whth monomer can prepare the macromolecular compound of this monomer.

Description

technical field [0001] The invention relates to a method for preparing a polymer compound by using an ionic liquid polymerization initiation system. The polymerization initiation system is composed of methylimidazole organic acid salt ionic liquid ([mim][RCOO]) as the polymerization medium, R-X as the initiator and low-valence inorganic transition metal salt MXn as the catalyst. The polymerization initiation system does not add any Transition metal organic ligands. Background technique [0002] In 1995, Wang Jinshan first reported in J.Am.chem.Soc., 1995,117,5614 in the atomic group transfer radical polymerization (abbreviated ATRP) initiation system, as initiator is alkyl halide hydrocarbon R-X, wherein X is CI and Br, and R is an organic group with conjugation inducing effect. In the first-generation ATRP initiation system, CuX and organic ligands are mainly used as catalysts. Anbo and Granel in (Macromolecules, 1996, 29: 8576, 1074) used Ru and Ni complexes such as RuCl...

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): C08F20/14C08F12/08C08F4/00C08F297/00
Inventor 胡自强来国桥彭家建邱化玉蒋可志祝根平
Owner HANGZHOU NORMAL UNIVERSITY
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