Thermal behavior and pyrolysis products of modified organo-layered silicates as intermediates for in situ polymerization

2009 ◽  
Vol 86 (1) ◽  
pp. 74-81 ◽  
Author(s):  
Fabio Bertini ◽  
Maurizio Canetti ◽  
Giuseppe Leone ◽  
Incoronata Tritto
e-Polymers ◽  
2007 ◽  
Vol 7 (1) ◽  
Author(s):  
Orietta Monticelli ◽  
Zenfira Musina ◽  
Francesca Ghigliotti ◽  
Saverio Russo ◽  
Valerio Causin

AbstractNanocomposites based on polyamide 6 (PA6) and montmorillonite-type (MMT) commercial clays, either unmodified or organically modified, were prepared by in-situ polymerization of ε-caprolactam (CL). The above materials were characterized in detail by a number of experimental techniques, including transmission electron microscopy (TEM), wide angle X-ray diffraction (WAXD), infrared spectroscopy (FTIR) and differential scanning calorimetry (DSC). The formation of nanostructured systems was checked not only for the commonly used ω-aminoacid-modified clay, but also for other types of organoclays. In general, a correlation was found between nanoscopic swelling of the clay in molten CL, measured by X-ray diffraction, and level of clay dispersion in PA6. Specifically, with the most swellable clays, completely exfoliated nanocomposites were obtained. However, also layered silicates modified by compatibilizers having carboxy groups, because of the active role of latter in CL polymerization, formed delaminated nanocomposites despite their low degree of swelling in CL monomer. Both molecular mass and crystallinity of the polyamide matrix were found to be strongly influenced by the presence of specific layered silicates. In particular, some characterization techniques (WAXD, FTIR) have evidenced a close relationship between the MMT used and PA6 crystal structure. Namely, PA6 γ-form is promoted by clay with compatibilizer bearing the carboxy group, which is able to induce the polymer to be tethered on the silicate layers, thus provoking conditions of restricted mobility to occur.


2010 ◽  
Vol 24 (01n02) ◽  
pp. 148-156 ◽  
Author(s):  
ARIADNE L. JUWONO ◽  
RIWANDI SIHOMBING ◽  
YUNI K. KRISNANDI ◽  
SUTARNO ◽  
HANDOKO SUBAWI ◽  
...  

Organo layered silicates (OLS) were successfully synthesized from Tapanuli clay through an intercalated ultrasonic method using hexadecyltrimethylamonium bromide ( HDTMABr ) as a cation exchange agent. Tapanuli clay–epoxy nanocomposites were also successfully synthesized with an in-situ polymerization. X-Ray Diffraction and Transmission Electron Microscope (TEM) results demonstrated a pattern of clay morphology typically found in nanocomposite systems. Although the nanocomposites' diffractogram showed an exfoliation structure, the TEM findings confirmed that the OLS d -spacing is between 2.58 nm (the minimum value) up to 14.74 nm (the maximum value); which indicates the nanocomposites posses a mixed structure between intercalated and exfoliated structures. It was found that the presence of 1wt% Tapanuli organo clay in the epoxy systems provides higher stiffness and higher Heat Deflection Temperature by 30 % and 7 % respectively.


Polymers ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 2742
Author(s):  
Ignazio Blanco ◽  
Gianluca Cicala ◽  
Claudio Tosto ◽  
Francesco Agatino Bottino

A comprehensive kinetics degradation study is carried out on novel multiple cages polyhedral oligomeric silsesquioxane (POSS)/polystyrene (PS) composites at 5% (w/w) of POSS to assess their thermal behavior with respect to the control PS and other similar POSS/PS systems studied in the past. The composites are synthesized by in situ polymerization of styrene in the presence of POSSs and characterized by 1H-NMR. The characteristics of thermal parameters are determined using kinetics literature methods, such as those developed by Kissinger and Flynn, Wall, and Ozawa (FWO), and discussed and compared with each other and with those obtained in the past for similar POSS/PS composites. A good improvement in the thermal stability with respect to neat polymer is found, but not with respect to those obtained in the past for polystyrene reinforced with single- or double-POSS cages. This behavior is attributed to the greater steric hindrance of the three-cages POSS compared with those of single- or double-cage POSS molecules.


2003 ◽  
Vol 49 (5) ◽  
pp. 329-335 ◽  
Author(s):  
Seok-Ho Hwang ◽  
Se-Woong Paeng ◽  
Jang-Yup Kim ◽  
Wansoo Huh ◽  
Sang-Won Lee

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