참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethyl sebacate | HCID 7829 | — |
| 반응물 | Trimethyl Phosphate | HCID 10541 | — |
| 반응물 | Oxo(oxostibanyloxy)stibane | HCID 27652 | — |
| 반응물 | Dimethyl-2,6-naphthalenedicarboxylate | HCID 61225 | — |
| 촉매 | Manganese acetate tetrahydrate | HCID 93021 | — |
| 용매 | Ethylene Glycol | HCID 174 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | Sebacic Acid | HCID 5192 | — |
반응 단계
Dimethyl 2,6-naphthalenedicarboxylate and dimethyl sebacate were dispersed in ethylene glycol. Then, 0.029 part of manganese acetate tetrahydrate, 0.028 parts of antimony trioxide and 0.1% of spherical silica particles having a mean particle size of 0.3 μm were added to 100 parts of the total of dimethyl 2,6-naphthalenedicarboxylate and dimethyl sebacate, and heated with stirring to conduct the reaction. The temperature was elevated to 235° C. while removing methanol produced as a by-product. After the by-production of methanol was completed, 0.03 part of trimethyl phosphate was added thereto. Then, the pressure was reduced to 0.3 Torr while elevating the temperature to 285° C., thereby conducting the polymerization. Dyes described in JP-A-7-168309, compounds 1-6 and I-24, were each further added to the solid matter in an amount of 54 ppm. The copolymerization ratio of sebacic acid (SA) and the intrinsic viscosity of a polyester thus obtained are shown in Table II-1.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06518004B2 |
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| 출처 데이터셋 | uspto-grants-2003_02 |
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| ORD ID | ord-be10107388c34ce9b8324216b15c00ad |
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| 출처 메모 | uspto-grants-2003_02 |
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