Method for preparing macromolecular weight branched polycaprolactone
A technology of polycaprolactone and high molecular weight, applied in the field of preparing branched polycaprolactone, which can solve the problems of difficult control, complex reaction and high cost
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
example 1
[0029] Add 2.0g of EVOH with 44% ethylene content into a 100ml reactor, evacuate and fill nitrogen three times repeatedly, then add 20ml ε-caprolactone, put it in an oil bath at 150°C, and after one hour, all EVOH dissolves into ε-caprolactone lactone, then lower the temperature to 110°C and add Sn(Oct) 2 0.020g, reacted for 20 hours. Dissolve in chloroform and precipitate into cold heptane. The molecular weight of the product is 123260; the conversion rate is 73.71%; the viscosity measured by Ubbelohde's viscometer is 0.48dL / g; the melting temperature of the obtained polymer measured by DSC is 36.4°C, and the crystallization temperature is 3.10°C.
example 2
[0031] The condition is the same as example 1, but the initiator is changed into EVOH with an ethylene content of 32%, and the reaction time is 48 hours. The molecular weight of the product is 146880; the conversion rate is 81.99%; the viscosity measured by Ubbelohde's viscometer is 0.61dL / g; the melting temperature of the obtained polymer measured by DSC is 41.7°C, and the crystallization temperature is 8.02°C.
example 3
[0033] Condition is the same as example 1, but changing initiator into EVOH with ethylene content of 27%, the molecular weight of product is 168470; Transformation efficiency is 85.67%; Its viscosity measured by Ubbelohde's viscometer is 0.67dL / g; Measure gained with DSC The melting temperature of the polymer was 39.4°C and the crystallization temperature was 5.4°C.
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 