Preparation and properties of layered double hydroxide/poly(ethylene terephthalate) nanocomposites by direct melt compounding

Polymer ◽  
2006 ◽  
Vol 47 (4) ◽  
pp. 1364-1371 ◽  
Author(s):  
Wan Duk Lee ◽  
Seung Soon Im ◽  
Hyung-Mi Lim ◽  
Kwang-Jin Kim
RSC Advances ◽  
2016 ◽  
Vol 6 (70) ◽  
pp. 65291-65298 ◽  
Author(s):  
Tsung-Yen Tsai ◽  
Naveen Bunekar

Poly(ethylene terephthalate)-layered double hydroxide (PET–LDH) composites were prepared by intercalation, followed by in situ polymerization.


2002 ◽  
Vol 10 (4) ◽  
pp. 221-229 ◽  
Author(s):  
Su-Chul Chung ◽  
Wan-Gyu Hahm ◽  
Seung-Soon Im ◽  
Seong-Geun Oh

2017 ◽  
Vol 2017 ◽  
pp. 1-9 ◽  
Author(s):  
Basheer A. Alshammari ◽  
Arthur N. Wilkinson ◽  
Ghzzai Almutairi

Graphite nanoplatelets (GNP) were incorporated with poly(ethylene terephthalate) (PET) matrix by melt-compounding technique using minilab compounder to produce PET-GNP nanocomposites, and then the extruded nanocomposites were compressed using compression molding to obtain films of 1 mm thickness. Percolation threshold value was determined using percolation theory. The electrical conductivity, morphology, and thermal behaviors of these nanocomposites were investigated at different contents of GNP, that is, below, around, and above its percolation threshold value. The results demonstrated that the addition of GNP at loading >5 wt.% made electrically conductive nanocomposites. An excellent electrical conductivity of ~1 S/m was obtained at 15 wt.% of GNP loading. The nanocomposites showed a typical insulator-conductor transition with a percolation threshold value of 5.7 wt.% of GNP. In addition, increasing screw speed enhanced the conductivity of the nanocomposites above its threshold value by ~2.5 orders of magnitude; this behavior is attributed to improved dispersion of these nanoparticles into the PET matrix. Microscopies results exhibited no indication of aggregations at 2 wt.% of GNP; however, some rolling up at 6 wt.% of GNP contents was observed, indicating that a conductive network has been formed, whereas more agglomeration and rolling up could be seen as the GNP content is increased in the PET matrix. These agglomerations reduced their aspect ratio and then reduced their reinforcement efficiency. NP loading (>2 wt.%) increased degree of crystallinity and improved thermal stability of matrix slightly, suggesting that 2 wt.% of GNP is more than enough to nucleate the matrix.


2007 ◽  
Vol 19 (5-6) ◽  
pp. 565-580 ◽  
Author(s):  
Doris Pospiech ◽  
Andreas Korwitz ◽  
Hartmut Komber ◽  
Dieter Voigt ◽  
Dieter Jehnichen ◽  
...  

The goal of the work presented here was to develop nanocomposites consisting of layered silicates and poly(ethylene terephthalate) (PET). Two nanocomposite preparation methods were compared: first, the usual melt compounding technique, and second, in-situ synthesis of PET in presence of different types of layered silicates. Montmorillonite (MMT) without and with organophilic modification was employed as layered silicate. In most cases, PETs with acceptable properties (molecular weight and discoloration) were synthesized in presence of different MMTs although the molecular weights of the in-situ PETs were lower than the control sample. These materials were used as masterbatch for PET nanocom-posites with 5 wt.% inorganic content. The exfoliation in both types of nanocomposites was not complete, but they showed a good distribution of clay within the polymer matrix.


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