反应 #2314302

反应方程式

glycolide

tartaric acid

stannous octoate

→

Glycolide Tartaric Acid

反应条件

后处理

1. 1
   其他A flame-dried resin kettle equipped with a mechanical stirrer and an argon inlet
2. 2
   其他The polymerization reactor and its contents were purged with dry argon several times
3. 3
   workup.ADDITIONcharge
4. 4
   温度the reactants were heated to and
5. 5
   其他to precipitate from the melt
6. 6
   其他Shortly after partial precipitation
7. 7
   其他the stirring was terminated
8. 8
   其他At the conclusion of the polymerization
9. 9
   其他was lowered below 120° C.
10. 10
    其他excess monomer was removed under reduced pressure
11. 11
    其他the polymer melting temperature (Tm=204° C.)
12. 12
    洗涤The resulting microparticles were rinsed with acetone
13. 13
    其他to remove trace amounts of monomer and low molecular weight oligomers
14. 14
    其他The product was then dried under reduced pressure at 40° C.

实验过程

A flame-dried resin kettle equipped with a mechanical stirrer and an argon inlet was charged with glycolide (2.586 mole, 300 g), anhydrous tartaric acid (0.172 mole, 26.8 g), and stannous octoate (0.2 M in toluene, 862 ml, 0.0172 mmole). The polymerization reactor and its contents were purged with dry argon several times. After melting the polymerization charge, the reactants were heated to and stirred at 160° C. until the polymer started to precipitate from the melt. Shortly after partial precipitation, the stirring was terminated and the reaction was continued at 160° C. for 2 hours. At the conclusion of the polymerization, the temperature was lowered below 120° C. and excess monomer was removed under reduced pressure. The composition of the isolated polymer was verified using infrared and NMR spectroscopy. Differential Scanning Calorimetry was used to determine the polymer melting temperature (Tm=204° C.). The solid polymer was ground to achieve average particle diameter of about 125 μm using a Wiley mill. Further reduction of the particle size to 5-10 m diameter was achieved using a jet-mill receiving pressurized dry nitrogen. The resulting microparticles were rinsed with acetone to remove trace amounts of monomer and low molecular weight oligomers. The product was then dried under reduced pressure at 40° C. until used. The average diameter of the dry microparticle was determined using a particle size analyzer.

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