Effect of trivalent ions containing layered hydroxide acetate on the thermal stability and flame retardancy of poly (methyl methacrylate) composite

2020 ◽  
Author(s):  
Pinki Chakraborty ◽  
Rajamani Nagarajan
Keyword(s):  
Thermal Stability ◽  
Methyl Methacrylate ◽  
Flame Retardancy ◽  
Poly Methyl Methacrylate

Enhanced Thermal Stability and Flame Retardancy of a Novel Transparent Poly(Methyl Methacrylate)-Based Copolymer

2014 ◽  
Vol 911 ◽  
pp. 423-427
Author(s):  
Sai Hua Jiang ◽  
Siu Ming Lo ◽  
Yuan Hu
Keyword(s):  
Thermal Stability ◽  
Methyl Methacrylate ◽  
Flame Retardant ◽  
Flame Retardancy ◽  
Chemical Structure ◽  
Poly Methyl Methacrylate ◽  
H Nmr ◽  
Char Formation ◽  
Phosphorus Containing ◽  
Thermal Stability Of

A novel poly (methyl methacrylate) (PMMA) based copolymer was synthesized by bulk copolymerization of methyl methacrylate (MMA) and a phosphorus-containing monomer, acryloxyethyl phenoxy phosphorodiethyl amidate (AEPPA). The chemical structure of AEPPA was confirmed by FTIR,1H NMR and31P NMR. The structure of copolymers was characterized using FTIR. TGA results indicate that the thermal stability of copolymers was remarkably enhanced with the addition of APEEA. LOI and MCC results suggest that the flame retardancy of copolymers was also improved. Detailed flame-retardant mechanism is proposed. The char formation during degradation caused by APEEA plays a key role in the property improvements.

scholarly journals Mono-acrylated isosorbide as a bio-based monomer for the improvement of thermal and mechanical properties of poly(methyl methacrylate)

RSC Advances ◽  
2019 ◽  
Vol 9 (61) ◽  
pp. 35532-35538 ◽  
Author(s):  
Dinghua Yu ◽  
Juan Zhao ◽  
Wenjuan Wang ◽  
Jingjie Qi ◽  
Yi Hu
Keyword(s):  
Mechanical Properties ◽  
Thermal Stability ◽  
Methyl Methacrylate ◽  
Thermal And Mechanical Properties ◽  
Poly Methyl Methacrylate

With bio-based monoester of acrylated isosorbide as the comonomer, copolymerized poly(methyl methacrylate) showed improved thermal stability and mechanical properties.

Synthesis and thermal decomposition kinetics of poly(methyl methacrylate)-b-poly(styrene) block copolymers

2015 ◽  
Vol 30 (5) ◽  
pp. 691-706 ◽  
Author(s):  
Xinghua Guan ◽  
Xiaoyan Ma ◽  
Hualong Zhou ◽  
Fang Chen ◽  
Zhiguang Li
Keyword(s):  
Thermal Stability ◽  
Thermal Decomposition ◽  
Weight Loss ◽  
Block Copolymers ◽  
Methyl Methacrylate ◽  
Terminal Group ◽  
Loss Ratio ◽  
Poly Methyl Methacrylate ◽  
Second Stage ◽  
Weight Loss Ratio

Two diblock copolymers of poly(methyl methacrylate)- block-poly(styrene) with chlorine as terminal group (PMMA- b-PS-Cl) were synthesized via two-step atom transfer radical polymerization. The structures of the block copolymers were characterized by Fourier transform infrared spectroscopy, proton nuclear magnetic resonance, and gel permeation chromatography. Thermal properties including glass transition temperature ( Tg) and thermal stability were studied by differential scanning calorimetry and thermogravimetric analysis (TGA), respectively. The block copolymers of PMMA- b-PS-Cl exhibited two glass transitions, which were attributed to the Tgs of PMMA and PS segments, respectively. According to TGA, thermal decompositions of PMMA macro-initiator and PMMA- b-PS-Cl block copolymers had two stages. The weight loss ratio in the second stage was more significant than that in the first stage, which may be attributed to the separation of the halogen atom from the terminal group and the formation of a double bond. The breaking down of the backbone dominates in the second stage in which the weight loss ratio was more than 70%, represented the main stage of pyrolysis. It was found that the introduction of the PS chain remarkably enhanced the thermal stability of the copolymer, thus endowing the block copolymers high activation energy for thermal decomposition. On the other hand, the remaining two pyrolysis procedures further indicated that thermodynamic mechanism didn’t change due to the introduction of PS segments.

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