Preparation method of organic zinc catalyst and poly(alkylene carbonate) resin

US10047032B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10047032-B2
Application numberUS-201514734856-A
CountryUS
Kind codeB2
Filing dateJun 9, 2015
Priority dateJun 13, 2014
Publication dateAug 14, 2018
Grant dateAug 14, 2018

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

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The present invention relates to a preparation method of an organic zinc catalyst capable of preparing an organic zinc catalyst having a finer and more uniform particle size and more improved activity during a polymerization process for preparing a poly(alkylene carbonate) resin, and a preparation method of a poly(alkylene carbonate) resin using the organic zinc catalyst. The preparation method of an organic zinc catalyst includes reacting a zinc precursor and a dicarboxylic acid in the presence of a dispersant to form a zinc dicarboxylate-based catalyst, wherein a reaction step is performed under a condition at which the number of moles of the dicarboxylic acid present in a reaction system is larger than that of the zinc precursor throughout the entire reaction step.

First claim

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What is claimed is: 1. A preparation method of an organic zinc catalyst, the preparation method comprising: providing a zinc precursor surface-treated with a dispersant; and reacting the surface-treated zinc precursor with a dicarboxylic acid having 3 to 20 carbon atoms to form a zinc dicarboxylate-based catalyst, wherein the reaction step is performed under a condition at which the number of moles of the dicarboxylic acid present in a reaction system is larger than that of the zinc precursor throughout the entire reaction step, wherein the dispersant is an anionic surfactant. 2. The preparation method of claim 1 , wherein the dispersant is an alkyl phenol ethoxylated phosphate ester represented by the following Chemical Formula 1: wherein, in Chemical Formula 1, R 1 to R 3 are each independently hydrogen or a straight or branched chain alkyl group having 8 to 12 carbon atoms, at least one of R 1 to R 3 being a straight or branched chain alkyl group having 8 to 12 carbon atoms; M 1 and M 2 are each independently hydrogen, ammonium, or a monovalent metal ion; and n is an integer of 3 to 100. 3. The preparation method of claim 1 , wherein the zinc precursor surface treated by the dispersant is formed by mixing the zinc precursor with the dispersant in a solvent. 4. The preparation method of claim 3 , wherein the dispersant is mixed at a content of 0.01 to 10 wt % with respect to the zinc precursor. 5. The preparation method of claim 1 , wherein the dicarboxylic acid is used in a ratio of 1.05 to 1.5 moles based on 1 mole of the zinc precursor. 6. The preparation method of claim 1 , wherein the zinc precursor includes a zinc compound selected from the group consisting of zinc oxide, zinc sulfate (ZnSO 4 ), zinc chlorate (Zn(ClO 3 ) 2 ), zinc nitrate (Zn(NO 3 ) 2 ), zinc acetate (Zn(OAc) 2 ), and zinc hydroxide. 7. The preparation method of claim 1 , wherein the dicarboxylic acid having 3 to 20 carbon atoms includes an aliphatic dicarboxylic acid selected from the group consisting of malonic acid, glutaric acid, succinic acid, and adipic acid, or an aromatic dicarboxylic acid selected from the group consisting of terephthalic acid, isophthalic acid, homophthalic acid, and phenyl glutaric acid. 8. The preparation method of claim 1 , wherein the reaction step is performed in a liquid medium, while adding a solution or dispersion containing the zinc precursor in portions 2 times or more to a solution or dispersion containing the dicarboxylic acid. 9. The preparation method of claim 8 , wherein the reaction step is performed while adding a solution or dispersion containing the zinc precursor at an amount obtained by dividing the entire use amount of the zinc precursor into 2 to 10 to the solution or dispersion containing the dicarboxylic acid at the same time interval. 10. The preparation method of claim 8 , wherein the reaction step is performed while dripping the solution or dispersion containing the zinc precursor in a droplet form into the solution or dispersion containing the dicarboxylic acid. 11. The preparation method of claim 8 , wherein the liquid medium includes one or more kinds of solvents selected from the group consisting of toluene, hexane, dimethylformamide, ethanol, and water. 12. The preparation method of claim 1 , wherein the organic zinc catalyst is in a form of particles having an average particle size of 0.5 μm or less. 13. The preparation method of claim 1 , wherein the organic zinc catalyst having a surface area of 1.8 m 2 /g or more is prepared.

Assignees

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Classifications

  • Glutaric acid · CPC title

  • C07C51/418Primary

    Preparation of metal complexes containing carboxylic acid moieties · CPC title

  • and cyclic ethers · CPC title

  • characterised by dimensions, e.g. grain size (in a colloidal state B01J35/23; crystallite size B01J35/77) · CPC title

  • Other (co) polymerisation, e.g. of lactides or epoxides · CPC title

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What does patent US10047032B2 cover?
The present invention relates to a preparation method of an organic zinc catalyst capable of preparing an organic zinc catalyst having a finer and more uniform particle size and more improved activity during a polymerization process for preparing a poly(alkylene carbonate) resin, and a preparation method of a poly(alkylene carbonate) resin using the organic zinc catalyst. The preparation method…
Who is the assignee on this patent?
Lg Chemical Ltd
What technology area does this patent fall under?
Primary CPC classification C07C51/418. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Aug 14 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).