Thermal degradation kinetics and flame-retardant properties of acrylonitrile butadiene styrene/thermoplastic polyurethanes/halloysite nanotubes and nanocomposites

Author(s):  
Huiwen Yu ◽  
Baiping Xu ◽  
Wenliu Zhuang ◽  
Meigui Wang ◽  
Hongwu Wu
2014 ◽  
Vol 1053 ◽  
pp. 263-267 ◽  
Author(s):  
Xiu Juan Tian

Thermal stability and thermal degradation kinetics of epoxy resins with 2-(Diphenylphosphinyl)-1, 4-benzenediol were investegated by thermogravimetric analysis (TGA) at different heating rates of 5 K/min, 10 K/min, 20 K/min and 40 K/min. The thermal degradation kinetic mechanism and models of the modified epoxy resins were determined by Coast Redfern method.The results showed that epoxy resins modified with the flame retardant had more thermal stability than pure epoxy resin. The solid-state decomposition mechanism of epoxy resin and the modified epoxy resin corresponded to the controlled decelerating ځ˽̈́˰̵̳͂͆ͅ˼˰̴̱̾˰̸̵̈́˰̵̸̳̱̹̽̾̓̽˰̶̳̹̾̈́̿̾̓ͅ˰̶˸ځ˹˰̵̵͇͂˰̃˸́˽ځ˹2/3. The introduction of phosphorus-containing flame retardant reduced thermal degradation rate of epoxy resins in the primary stage, and promote the formation of carbon layer.


2018 ◽  
Vol 31 (1) ◽  
pp. 86-96 ◽  
Author(s):  
R Vini ◽  
S Thenmozhi ◽  
SC Murugavel

In this study, azomethine polyphosphonates were synthesized by solution polycondensation of phenylphosphonic dichloride with various azomethine diols such as [4-(4-hydroxy phenyl) iminomethyl] phenol, [(4-(4-hydroxy-3-methoxy phenyl) iminomethyl)] phenol and [4-(4-hydroxy-3-ethoxy phenyl) iminomethyl] phenol using triethylamine catalyst at ambient temperature. The structure of the synthesized polymers was confirmed by Fourier transform infrared and 1H-, 13C- and 31P- nuclear magnetic resonance spectroscopic techniques. Thermal properties of the polymers were studied by thermogravimetric analysis (TGA) and differential scanning calorimetry under nitrogen atmosphere. The TGA data showed that the synthesized polyphosphonates produce high char yield at 600°C due to the presence of phosphorous atom in the polymer chain and hence have good flame-retardant properties. One of the synthesized polyphosphonate was blended with commercial diglycidyl ether of bisphenol-A (DGEBA) resin in various weight percentage and cured with commercial curing agent triethylene tetramine (TETA). The polyphosphonates-blended epoxy thermosets have tensile strength in the range of 5–41 MPa and the percentage of elongation at breaks was 4–18. It was found that the incorporation of polyphosphonates into epoxy thermoset decreased the tensile strength from 41 MPa to 5 MPa, whereas the elongation at break value increased with increase in the weight percentage of polyphosphonate. The influence of polyphosphonates on the flame retardancy of blended thermosets was examined by limiting oxygen index (LOI) and vertical burning (UL-94) tests and found that the polymer samples achieved an increased UL-94 rating and the LOI values were in the range of 24–26. Broido and Horowitz–Metzger methods have been used to study the thermal degradation kinetic parameters.


2012 ◽  
Vol 61 (6) ◽  
pp. 926-933 ◽  
Author(s):  
Zahra Derakhshesh ◽  
Manouchehr Khorasani ◽  
Shahin Akhlaghi ◽  
Bahram Keyvani ◽  
Ali Asghar Sabbagh Alvani

2014 ◽  
Vol 1004-1005 ◽  
pp. 253-256 ◽  
Author(s):  
Li Yan ◽  
Ji Meng Sang

A novel flame retardant additive, DOPO-based polymeric phosphate (PFR-D), which simultaneously contained phosphorus and sulfur, was synthesized from 9,10-dihyro-9-oxa-10-phosphaphnanthrene-10-oxide (DOPO), POCl3 and bisphenol S. And the structure of PFR-D has been characterized by 1H-NMR, 31P-NMR and FT-IR. PFR-D was used as additive in polycarbonate/acrylonitrile-butadiene-styrene alloy (PC/ABS). The UL94 V-0 rating was achieved by addition of 5-7% PFR-D in PC/ABS, the LOI reached 27.5%. The thermal degradation of PFR-D and polymers with it was investigated by TGA, and the results showed that addition of PFR-D apparently changed the pyrolysis pathways of PC/ABS. The TGA curves indicated that the flame retardant effect was attributed to promoting the char yield by involving the polymer in charring.


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