# US 2017/0283533 A1 · Method of preparing vinyl chloride-based copolymer and vinyl chloride-based copolymer prepared thereby > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 2017/0283533 A1 - Document ID: US20170283533A1 - Status: Published application - Kind: A1 - Application number: 15/508,326 - Filed: 2016-06-03 - Published: 2017-10-05 - Earliest claimed: 2015-06-05 - Assignees: LG Chem, Ltd. - Applicants: LG Chem, Ltd. - Inventors: Seong Yong AHN; Kun Ji KIM; Se Woong LEE; Bhom Ri KIM - Web page: https://patentgrep.com/patent/US20170283533A1 ## CPC - C08F 214/06: Vinyl chloride - C08F: MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS ## Abstract The present invention relates to a method of preparing a vinyl chloride-based copolymer having excellent plasticity and processability, a vinyl chloride-based copolymer prepared thereby, a thermoplastic resin composition including the vinyl chloride-based copolymer, and a thermoplastic resin molded article prepared from the composition. Since the preparation method may improve copolymerizability with a vinyl chloride-based monomer by continuously adding or dividedly adding an unsaturated fatty acid ester mixture used as a comonomer during the time of specific polymerization conversion rate, the unreacted unsaturated fatty acid ester mixture may be reduced, and, as a result, the conversion rate of the vinyl chloride-based copolymer may be significantly improved. Thus, plasticity and processability of a vinyl chloride-based copolymer prepared by the above method may be significantly improved. ## Claims ### Claim 1 A method of preparing a vinyl chloride-based copolymer, the method comprising adding an unsaturated fatty acid ester mixture to a vinyl chloride-based monomer and performing polymerization, wherein the adding is performed by continuous addition or divided addition of at least two times at a polymerization conversion rate of 35% or less. ### Claim 2 (depends on 1) The method of claim 1, wherein the unsaturated fatty acid ester mixture is a mixture of a cis isomer of an unsaturated fatty acid ester and a trans isomer of the unsaturated fatty acid ester, and the cis isomer of the unsaturated fatty acid ester and the trans isomer of the unsaturated fatty acid ester in the mixture have a weight ratio of 60:40 to 99:1. ### Claim 3 (depends on 2) The method of claim 2, wherein the cis isomer of the unsaturated fatty acid ester and the trans isomer of the unsaturated fatty acid ester in the mixture have a weight ratio of 65:35 to 90:10. ### Claim 4 (depends on 2) The method of claim 2, wherein the cis isomer of the unsaturated fatty acid ester is a compound represented by Formula 1, and the trans isomer of the unsaturated fatty acid ester is a compound represented by Formula 2: in Formula 1 or 2, R1 to R4 are each independently selected from the group consisting of an alkyl group having 2 to 16 carbon atoms, a cycloalkyl group having 3 to 16 carbon atoms, and a combination thereof. ### Claim 5 (depends on 1) The method of claim 1, wherein the continuous addition is performed in which the addition is started when the polymerization conversion rate is 1% or more, the addition is terminated when the polymerization conversion rate is 35% or less, and an entire amount of the mixture used is added at a constant rate from the start to the termination of the addition. ### Claim 6 (depends on 1) The method of claim 1, wherein the divided addition is performed in which a first fraction of an entire amount of the mixture is primarily added when the polymerization conversion rate is in a range of 1% to 15%, and a remaining second fraction, excluding the first fraction, of the entire amount of the mixture is secondarily added when the polymerization conversion rate is in a range of 25% to 35%. ### Claim 7 (depends on 6) The method of claim 6, wherein the first fraction and the second fraction have a weight ratio of 9:1 to 1:9. ### Claim 8 (depends on 1) The method of claim 1, wherein the polymerization is performed by suspension polymerization in a solvent in the presence of a polymerization initiator and a protective colloid auxiliary. ### Claim 9 (depends on 8) The method of claim 8, wherein the protective colloid auxiliary is one selected from the group consisting of a vinyl alcohol-based resin, cellulose, and an unsaturated organic acid polymer, or a mixture of two thereof. ### Claim 10 (depends on 8) The method of claim 8, wherein the protective colloid auxiliary is a mixture in which a vinyl alcohol-based resin and cellulose are mixed in a weight ratio of 5:1 to 7:7, and the vinyl alcohol-based resin is a mixture in which a first polyvinyl alcohol having a degree of hydration of greater than 50 wt % and equal to or less than 90 wt % and a second polyvinyl alcohol having a degree of hydration of 30 wt % to 50 wt % are mixed in a weight ratio of 2:1 to 1:2. ### Claim 11 (depends on 1) The method of claim 1, wherein the unsaturated fatty acid ester mixture is used in an amount of 3 parts by weight to 53 parts by weight based on 100 parts by weight of the vinyl chloride-based monomer. ### Claim 12 (depends on 1) The method of claim 1, wherein the unsaturated fatty acid ester mixture is used in an amount of 20 parts by weight to 50 parts by weight based on 100 parts by weight of the vinyl chloride-based monomer. ### Claim 13 (depends on 1) A vinyl chloride-based copolymer prepared by the method of claim 1. ### Claim 14 (depends on 13) The vinyl chloride-based copolymer of claim 13, wherein the vinyl chloride-based copolymer comprises 65 wt % to 97 wt % of a vinyl chloride-based monomer-derived repeating unit; and 3 wt % to 35 wt % of an unsaturated fatty acid ester-derived repeating unit. ### Claim 15 (depends on 14) The vinyl chloride-based copolymer of claim 14, wherein the unsaturated fatty acid ester-derived repeating unit comprises a repeating unit derived from a cis isomer of the unsaturated fatty acid ester and a repeating unit derived from a trans isomer of the unsaturated fatty acid ester in a weight ratio of 60:40 to 99:1. ### Claim 16 (depends on 15) The vinyl chloride-based copolymer of claim 15, wherein the cis isomer of the unsaturated fatty acid ester is a compound represented by Formula 1, and the trans isomer of the unsaturated fatty acid ester is a compound represented by Formula 2: in Formula 1 or 2, R1 to R4 are each independently selected from the group consisting of an alkyl group having 2 to 16 carbon atoms, a cycloalkyl group having 3 to 16 carbon atoms, and a combination thereof. ### Claim 17 (depends on 13) The vinyl chloride-based copolymer of claim 13, wherein the vinyl chloride-based copolymer has a polydispersity of 1.5 to 2.5. ### Claim 18 (depends on 13) The vinyl chloride-based copolymer of claim 13, wherein the vinyl chloride-based copolymer has a weight-average molecular weight of 70,000 g/mol to 300,000 g/mol and a number-average molecular weight of 50,000 g/mol to 150,000 g/mol. ### Claim 19 (depends on 13) The vinyl chloride-based copolymer of claim 13, wherein the vinyl chloride-based copolymer has an average pore diameter of 100 nm or less and a porosity of 40 vol % or less. ### Claim 20 (depends on 13) The vinyl chloride-based copolymer of claim 13, wherein the vinyl chloride-based copolymer has a cold plasticizer absorption of 10 wt % or less. ### Claim 21 (depends on 13) The vinyl chloride-based copolymer of claim 13, wherein the vinyl chloride-based copolymer has a hardness of 50 HS to 110 HS. ### Claim at position 22 22-24. (canceled)