Organic zinc catalyst and preparation method thereof

Patent metadata

Field	Value
Publication number	US-9803048-B2
Application number	US-201414917898-A
Country	US
Kind code	B2
Filing date	Oct 30, 2014
Priority date	Nov 4, 2013
Publication date	Oct 31, 2017
Grant date	Oct 31, 2017

Abstract

An organic zinc catalyst and a preparation method thereof are provided. According to the present invention, the organic zinc catalyst has a smaller thickness and a larger surface area to exhibit more improved activity in polymerization for the preparation of a poly(alkylene carbonate) resin.

First claim

The invention claimed is:

1. A method of preparing an organic zinc catalyst, the method comprising:
reacting a zinc precursor and dicarboxylic acid having 3 to 20 carbon atoms to form zinc dicarboxylate-based particles in a liquid medium containing a polar solvent and a non-polar solvent at a volume ratio of 30:70 to 75:25,
wherein the zinc dicarboxylate-based particles formed by the reaction have an average particle thickness of 30 nm or less and an argon adsorption Brunauer-Emmett-Teller (BET) surface area of 20 m 2 /g or more.

2. The method of claim 1 , wherein the polar solvent is a solvent having a dielectric constant of 20 or more at 25° C. or lower, and the non-polar solvent is a solvent having a dielectric constant of less than 15 at 25° C. or lower.

3. The method of claim 1 , wherein the polar solvent is one or more compounds selected from the group consisting of methanol, ethanol, acetic acid, acetone, N,N-dimethylformamide, N,N-dimethylacetamide, propylene carbonate, acetonitrile, dimethyl sulfoxide, and hexamethylphosphotriamide.

4. The method of claim 1 , wherein the non-polar solvent is one or more compounds selected from the group consisting of toluene, benzene, xylene, diethylether, tetrahydrofuran, 1,4-dioxane, dimethylcarbonate, and diethylcarbonate.

5. The method of claim 1 , wherein the zinc precursor is one or more compounds selected from the group consisting of zinc oxide, zinc sulfoxide (ZnSO 4 ), zinc chlorate (Zn(ClO 3 ) 2 ), zinc nitrate (Zn(NO 3 ) 2 ), zinc acetate (Zn(OAc) 2 ), and zinc hydroxide.

6. The method of claim 1 , wherein the dicarboxylic acid having 3 to 20 carbon atoms is one or more compounds selected from the group consisting of malonic acid, glutaric acid, succinic acid, adipic acid, terephthalic acid, isophthalic acid, homophthalic acid, and phenylglutaric acid.

7. The method of claim 1 , wherein the dicarboxylic acid is used in an amount of about 1 to 1.5 mol, based on 1 mol of the zinc precursor.

8. The method of claim 1 , wherein the reaction is performed at a temperature of about 20 to 110° C. for 1 to 20 h.

Assignees

• Lg Chemical Ltd

Inventors

• Kang Seong Kyun
• Cho Hyun Ju
• Kim Sung-Kyoung
• Lee Jong Won
• Park Seung Young
• Choi Hyeon

Classifications

• C08G64/34 Primary

  and cyclic ethers · CPC title

• B01J31/12

  containing organo-metallic compounds or metal hydrides · CPC title

• C08G64/0208

  saturated · CPC title

• B01J35/613

  10-100 m2/g · CPC title

• B01J35/45

  Nanoparticles · CPC title