Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethyl terephthalate | HCID 8441 | — |
| Edukt | Dimethyl isophthalate | HCID 15088 | — |
| Edukt | Bisphenol-a ethyleneoxide | HCID 22406341 | — |
| Katalysator | Manganous Acetate | HCID 12525 | — |
| Lösungsmittel | Ethylene Glycol | HCID 174 | — |
| Produkt | Bisphenol A | HCID 6623 | — |
Reaktionsschritte
Dimethyl terephthalate, dimethyl isophthalate, ethylene glycol, bisphenol A-ethylene oxide (2 mols) adduct, and manganese acetate were deposit into a reactor installed with a heater, a stirrer, a rectification column, a pressure-reducing device and a thermometer, as in Table 17, and gradually heated in a nitrogen atmosphere up to a temperature falling between 160 and 220° C. over a period of about 4 hours to effect interesterification, while removing ethanol through distillation. Then, this was subjected to polycondensation under a reduced pressure of from 0.5 to 5.0 mmHg at 260° C. for about 2 hours. Thus were obtained bisphenol A-added polyester resins b-1 to b-4 as in Table 17. Each of the thus-obtained, bisphenol A-added polyester resins was dissolved in a mixed solvent of cyclohexanone/Solvesso 150 (50/50, by weight) to prepare a resin solution having a nonvolatile content of 40%. The molecular weight of each bisphenol A-added polyester resin being produced was controlled by varying the polycondensation time. The number-average molecular weight of each resin was measured in terms of polystyrene, through gel permeation chromatography.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06136455 |
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| Quelldatensatz | uspto-grants-2000_10 |
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| ORD ID | ord-19d1dfdc5b9b422e8580f27315188c89 |
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| Quellennotiz | uspto-grants-2000_10 |
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