In situ prepared PET nanocomposites: Effect of organically modified montmorillonite and fumed silica nanoparticles on PET physical properties and thermal degradation kinetics

2010 ◽  
Vol 500 (1-2) ◽  
pp. 21-29 ◽  
Author(s):  
A.A. Vassiliou ◽  
K. Chrissafis ◽  
D.N. Bikiaris
2009 ◽  
Vol 151 ◽  
pp. 129-134 ◽  
Author(s):  
Onur Yılmaz ◽  
Aurica P. Chiriac ◽  
Catalina Natalia Cheaburu ◽  
Loredana E. Nita ◽  
Gürbüz Gülümser ◽  
...  

Nanocomposites based on layered silicate organically modified montmorillonite (Cloisite 20A) and acrylic comonomers (butyl acrylate and methyl methacrylate) were prepared by simple “in situ” batch emulsion polymerization method. The particle size and zeta potential of the emulsions were analyzed. The structural characterizations of the nanocomposites were performed by FTIR, thermal behaviors of the films were investigated by DSC, mechanical properties of the films were tested by DMA and intercalation success was viewed by XRD. The mechanical properties of the nanocomposites were improved significantly especially at the temperatures above Tg. The ultrasonication process was found to be useful for increasing the homogeneity of the emulsions and intercalation success. The obtained nanocomposite emulsions were applied on garment leathers in a finishing formulation as aqueous binders sharing good film forming ability and elasticity.


2008 ◽  
Vol 8 (4) ◽  
pp. 1927-1936 ◽  
Author(s):  
Grace Chigwada ◽  
Everson Kandare ◽  
Dongyan Wang ◽  
Stephen Majoni ◽  
Darlington Mlambo ◽  
...  

Organically-modified montmorillonite (MMT) clays have been prepared using ammonium salts containing quinoline, pyridine, benzene, and styrenic groups. The nanocomposites were prepared by melt blending and the formation of nanocomposites was characterized using X-ray diffraction (XRD) and transmission electron microscopy (TEM). Thermal stability and flammability were evaluated by thermogravimetric analysis (TGA) and cone calorimetry measurements, respectively. The presence ofmodified MMT at 5% loading resulted in significant improvement in thermal stability compared to the virgin polymer. Effective activation energies for mass loss were determined via a model-free isoconversional approach from TGA data obtained under N2 and under air. The additives served to raise the activation energy, with a more significant impact observed under pyrolysis conditions. The onset temperature of degradation and temperature of maximum decomposition rate are increased, while the peak heat release rate and mass loss rates are significantly reduced in the presence of three of the modified clays. No reduction in the total heat released is observed.


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