Highly heat-resistant polycarbonate ester and preparation method therefor

1. A heat-resistant, bio-based polycarbonate ester, comprising:

a repeat unit 1 of the following Formula 1;

a repeat unit 2 of the following Formula 2; and

a repeat unit 3 of the following Formula 3:

wherein molar fractions of the repeat units 1 to 3 are x, y, and z, respectively, x being a real number of greater than 0 to less than 1, y being a real number of greater than 0 to 0.7, z being a real number of greater than 0 to 0.6, and the ratio of y:z being 2:1 to 3:5; and

wherein the polycarbonate ester has a glass transition temperature of 190 to 220° C.

2. The heat-resistant, bio-based polycarbonate ester of claim 1 , wherein the repeat unit 1 is obtained from a reaction of 1,4:3,6-dianhydrohexitol and a carbonate, the repeat unit 2 is obtained from a reaction of 1,4:3,6-dianhydrohexitol and 1,4-cyclohexanedicarboxylate, and the repeat unit 3 is obtained from a reaction of 1,4:3,6-dianhydrohexitol and a terephthalate.

3. The heat-resistant, bio-based polycarbonate ester of claim 1 , which is composed of the repeat units 1 to 3, and

wherein molar fractions of the repeat units 1 to 3 are x, y, and z, respectively, x being a real number of greater than 0 to 0.9, y being a real number of greater than 0 to 0.6, z being a real number of greater than 0 to 0.5, and x+y+z being 1.

4. A process for preparing a heat-resistant, bio-based polycarbonate ester, which comprises:

(1) converting a compound of the following Formula 4 to an intermediate reactant having a halogen functional group at the terminal thereof, followed by a nucleophilic reaction with phenol or a phenol substituent, or subjecting a compound of the following Formula 4 to a transesterification or esterification reaction with phenol or a phenol substituent, to prepare a compound of the following Formula 5; and

(2) subjecting compounds of the following Formulae 5 to 7 and 1,4:3,6-dianhydrohexitol to a melt polycondensation reaction to prepare a compound containing repeat units 1 to 3 of the following Formulae 1 to 3:

wherein R 1 is methyl or hydrogen,

R 2 and R 3 are each an alkyl group having 1 to 18 carbon atoms or an aryl group having 6 to 18 carbon atoms, wherein the aryl group optionally have at least one sub stituent selected from the group consisting of an alkyl group having 1 to 18 carbon atoms, a cycloalkyl group having 4 to 20 carbon atoms, an aryl group having 6 to 18 carbon atoms, an alkoxy group having 1 to 18 carbon atoms, a cycloalkoxy group having 4 to 20 carbon atoms, an aryloxy group having 6 to 18 carbon atoms, an alkylsulfonyl group having 1 to 18 carbon atoms, a cycloalkylsulfonyl group having 4 to 20 carbon atoms, an arylsulfonyl group having 6 to 18 carbon atoms, and an ester substituent,

wherein molar fractions of the repeat units 1 to 3 are x, y, and z, respectively, x being a real number of greater than 0 to less than 1, y being a real number of greater than 0 to 0.7, z being a real number of greater than 0 to 0.6, and the ratio of y:z being 2:1 to 3:5; and

wherein the polycarbonate ester has a glass transition temperature of 190 to 220° C.

5. The process for preparing a heat-resistant, bio-based polycarbonate ester of claim 4 , wherein the heat-resistant, bio-based polycarbonate ester is composed of the repeat units 1 to 3, and wherein x+y+z is 1.

6. The process for preparing a heat-resistant, bio-based polycarbonate ester of claim 4 , wherein the intermediate reactant having a halogen functional group at the terminal thereof is a compound represented by the following Formula 8:

wherein R 4 is each independently F, Cl, or Br.

7. The process for preparing a heat-resistant, bio-based polycarbonate ester of claim 6 , wherein the molar ratio of the compound of the above Formula 8 to phenol or the phenol substituent in the nucleophilic reaction of the above step (1) is 1:1 to 5.

8. The process for preparing a heat-resistant, bio-based polycarbonate ester of claim 4 , wherein the intermediate reactant having a halogen functional group at the terminal thereof is prepared by reacting the compound represented by the above Formula 4 with a halogenated compound, and

the halogenated compound is at least one selected from the group consisting of phosgene, triphosgene, thionyl chloride, oxalyl chloride, phosphorus trichloride, phosphorus pentachloride, phosphorus pentabromide, and cyanuric fluoride.

9. The process for preparing a heat-resistant, bio-based polycarbonate ester of claim 4 , wherein the conversion to the intermediate reactant in the above step (2) is carried out under atmospheric pressure at a temperature of −30 to 150° C. for 5 minutes to 48 hours.

10. The process for preparing a heat-resistant, bio-based polycarbonate ester of claim 4 , wherein the compound of the above Formula 7 is diphenyl carbonate or substituted diphenyl carbonate.

11. The process for preparing a heat-resistant, bio-based polycarbonate ester of claim 4 , wherein the transesterification or esterification reaction in the above step (1) is carried out at 20 to 300° C.

12. The process for preparing a heat-resistant, bio-based polycarbonate ester of claim 4 , wherein the molar ratio of the compound of the above Formula 4 to phenol or the phenol substituent in the transesterification or esterification reaction of the above step (1) is 1:2 to 40.

13. The process for preparing a heat-resistant, bio-based polycarbonate ester of claim 4 , wherein the melt polycondensation reaction in the above step (2) comprises:

(2-1) a first reaction step under a reduced pressure of 50 to 700 torr at a temperature of 130 to 250° C. for 0.1 to 10 hours; and

(2-2) a second reaction step under a reduced pressure of 0.1 to 20 torr at a temperature of 200 to 350° C. for 0.1 to 10 hours.