Polymers, co-polymers, and monomers using co2 as a reagent
US-2015376331-A1 · Dec 31, 2015 · US
US9447236B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9447236-B2 |
| Application number | US-201414421091-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 27, 2014 |
| Priority date | May 27, 2013 |
| Publication date | Sep 20, 2016 |
| Grant date | Sep 20, 2016 |
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The present invention relates to a method of manufacturing polyalkylene carbonate. More specifically, the method of manufacturing polyalkylene carbonate includes solution-polymerizing an epoxide compound and carbon dioxide in the presence of a cobalt complex having a neutral singe-site as a catalyst and a solvent, thereby providing stability and adjusting degree of polymerization and being advantageous for performing a post-treatment process after polymerization.
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What is claimed is: 1. A method of manufacturing polyalkylene carbonate comprising: solution-polymerizing an epoxide compound and continuously or non-continuously injected carbon dioxide in the presence of a catalyst represented by the following Chemical Formula 1 and 1,2-ethylene dichloride as a solvent, wherein the solvent is used at a weight ratio of 1:0.1 to 1:0.51 based on the epoxide compound: in Chemical Formula 1, Q is C1-C20 alkylene, C3-C20 cycloalkylene, C6-C30 arylene, or C1-C20 dioxy radical, including or not including halogen, nitrogen, oxygen, silicon, sulfur, or phosphorus atom, R 1 to R 7 are each independently or simultaneously, hydrogen; or a C1-C20 alkyl group, a C2-C20 alkenyl group, a C7-C20 alkylaryl group, or a C7-C20 arylalkyl group, including or not including at least one of halogen, nitrogen, oxygen, silicon, sulfur, and phosphorus atom, R 8 to R 13 are each independently hydrogen or a C1-C20 alkyl group, n is an integer of 1 to 10, and X is −Cl, −NO 3 or −OAc. 2. The method of claim 1 , wherein in Chemical Formula 1, R 1 , R 3 , R 5 and R 7 are each independently hydrogen or a C1-C20 alkyl group, R 2 , R 4 and R 6 are each independently a C1-C20 alkyl group, Q is C3-C20 cycloalkylene, n is an integer of 1 to 10, and X is —Cl, —NO 3 or —OAc. 3. The method of claim 2 , wherein in Chemical Formula 1, R 1 , R 3 , R 5 and R 7 are each independently hydrogen, R 2 , R 4 and R 6 are each independently a tert-butyl group, and Q is C3-C20 cycloalkylene. 4. The method of claim 1 , wherein the carbon dioxide is injected at a weight ratio of 0.5:1 to 10:1 based on the epoxide compound. 5. The method of claim 1 , wherein the solution-polymerizing is performed at a temperature of 50 to 100° C. for 30 minutes to 9 hours. 6. The method of claim 1 , wherein in the solution-polymerizing, an ammonium salt selected from the group consisting of (n-Bu) 4 NY (wherein Y═Cl or OAc), [PPN]Cl, [PPN]Br and [PPN]N 3 is further included as a cocatalyst. 7. The method of claim 1 , wherein the epoxide compound is at least one kind selected from the group consisting of C2-C20 alkylene oxide substituted or unsubstituted with halogen or a C1-C5 alkyl group; C4-C20 cycloalkylene oxide substituted or unsubstituted with halogen or a C1-C5 alkyl group; and C8-C20 styrene oxide substituted or unsubstituted with halogen or a C1-C5 alkyl group. 8. The method of claim 1 , wherein the epoxide compound includes C2-C20 alkylene oxide substituted or unsubstituted with halogen or a C1-C5 alkyl group, and has a carbonate linkage selectivity of 99% or more. 9. The method of claim 1 , wherein the polyalkylene carbonate includes polyethylene carbonate having a weight average molecular weight of 1000 to 500,000.
Other (co) polymerisation, e.g. of lactides or epoxides · CPC title
and cyclic ethers · CPC title
Cobalt · CPC title
Ligands with a porphyrin ring system or analogues thereof, e.g. phthalocyanines, corroles · CPC title
Organic complexes · CPC title
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