The acetylation of starch is a chemical modification, known for more than a century Jarowenko [1]. In the modified starch, part of the hydroxyl groups of the glucose monomers have been converted into o-(-ethanoate) groups. Highly acetylated starches with a degree of substitution (DS) of 2 to 3 were
Maleation of polylactide (PLA) by reactive extrusion
β Scribed by Denise Carlson; Li Nie; Ramani Narayan; Philippe Dubois
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 232 KB
- Volume
- 72
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
Free-radical-initiated grafting of maleic anhydride (MA) onto a polylactide (PLA) backbone was performed by reactive extrusion. A concentration of 2 wt % MA in the presence of 2,5-dimethyl-2,5-di-(tert-butylperoxy)hexane (Lupersol 101) as the freeradical initiator was used for all experiments. Two reaction temperatures were studied (180 and 200Β°C) with a peroxide initiator concentration between 0.0 and 0.5 wt %. Under these conditions, between 0.066 and 0.672 wt % MA was grafted onto the PLA chains. Triple-detector size-exclusion chromatography (TriSEC), melt flow index (MFI), and thermal gravimetric analysis (TGA) were used to characterize the maleated PLA polymers. Increasing the initiator concentration resulted in an increase in the grafting of MA, as well as a decrease in the molecular weight of the polymer. The maleation of PLA proved to be very efficient in promoting strong interfacial adhesion with corn native starch in composites as obtained by melt blending.
π SIMILAR VOLUMES
Maleic anhydride (MAn) was grafted onto aliphatic and aromatic/aliphatic copolyesters by reactive extrusion in the presence of a free radical initiator using a twin-screw extruder. The grafting reaction was confirmed by spectroscopic analyses. The presence of succinic anhydride groups was shown by F
The chain extension reaction in poly(butylene terephthalate) (PBT) melt was studied in detail. A high-reactivity diepoxy, diglycidyl tetrahydrophthalate, was used as a chain extender that can react with the hydroxyl and carboxyl end groups of PBT at a very fast reaction rate and a relatively high te