Process for producing polyhydroxy polyester
A technology for polyhydroxy polyester and its manufacturing method, which is applied in the field of polyhydroxy polyester manufacture, can solve the problems of reducing environmental load and effective utilization of straight-chain polyester that have not yet been reported, and achieves reducing environmental load, suppressing poor forming, The effect of efficient manufacturing
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Embodiment 1
[0041] 7 g of sorbitol was added to 200 g of polylactic acid (Unitaka Co., Ltd., TE-4000), and the mixture was heated and melted at 200°C for 4 hours under a nitrogen atmosphere to obtain a crude polyhydroxy polyester (P) (Comparative Example 1) . The molecular weight and carboxyl group concentration of the polyhydroxy polyester in this reaction change with time as figure 1 Shown. As the reaction progressed, the carboxyl groups increased, reaching 88 μmol / g.
[0042] P (10g) was melted at 200°C, 2.3% by mass of polycarbodiimide A (Nisshinbo Co., Ltd. V-05, carbodiimide equivalent: 261g / mol) was added to it, and then heated and mixed for 1 hour . The molecular weight and carboxyl group concentration of the obtained polyhydroxy polyester are shown in Table 1.
[0043] The molecular weight is measured by GPC (10A-VP, manufactured by Shimadzu Corporation).
[0044] The carboxyl group concentration was determined by dissolving a sample (100 mg) in a mixed solvent of chloroform (20 ml...
Embodiment 2
[0046] P (10g) was melted at 200°C, 5.0% by mass of polycarbodiimide B (V-02B, Nisshinbo Co., Ltd., carbodiimide equivalent 603 g / mol) was added thereto, and then heated and mixed for 1 hour . In the same manner as in Example 1, the molecular weight and carboxyl group concentration of the obtained polyhydroxy polyester were measured. The results are shown in Table 1.
Embodiment 3
[0048] P (10g) was melted at 200°C, 2.1% by mass of polycarbodiimide C (LA-1, Nisshinbo Co., Ltd., carbodiimide equivalent 247g / mol) was added thereto, and the mixture was heated and mixed for 1 hour . In the same manner as in Example 1, the molecular weight and carboxyl group concentration of the obtained polyhydroxy polyester were measured. The results are shown in Table 1.
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