19 research outputs found
The Effects of Nitrogen-Containing Monomers on the Thermal Degradation and Combustion Attributes of Polystyrenes Chemically Modified with Phosphonate Groups
In the present study, polystyrene (PS) is chemically modified with diethyl(acryloyloxymethyl)phosphonate (DEAMP) and an N-containing monomer, selected from different classes of compounds, via a ter-polymerization route; thus, exploring possible PâN synergistic effects on fire retardance of the base polymer. The successful incorporation of P and N monomeric units is confirmed by Fourier Transform Infrared (FT-IR), 1H and 31P Nuclear Magnetic Resonance (NMR) spectroscopies. The thermal degradation and combustion attributes of modified polymeric materials are measured using standard techniques, including Thermo-Gravimetric Analysis (TGA), Differential Scanning Calorimetry (DSC), âbombâ calorimetry, and Pyrolysis Combustion Flow Calorimetry (PCFC). The thermal and combustion studies demonstrate that the thermal stability and combustion characteristics of styrenic polymers are significantly altered by the presence of even nominal amounts of P- and N-containing groups, and in certain cases, synergistic interactions of these groups are also evident. For instance, as revealed by TGA, the extent of char formation, under the oxidative atmosphere, in the prepared ter-polymers, is enhanced by 16â44%, when compared to the unmodified PS. The heat release rates and heat release capacities of ter-polymers, measured using the PCFC technique, are reduced by 18â50%, in comparison to the same parameters obtained for the unmodified counterpart.</p
Artificial Heart Neural Networks An Idea
Artificial Neural Networks Field (ANN Field) is an exciting field of research. ANN field took its inspiration from Human Brain. The heart and Brain are very important for the survival of Humans. Research Scientists published many articles by giving importance to Brain. But scientists have not yet explored much on the Heart which is another important part in addition to the Brain. The primary purpose of publishing this article is to show a path to ANN field Research Scientists by introducing the concept of Heart into Artificial Neural Networks. In this paper, we coined and defined Artificial Heart Neuron, which is the basic part of Artificial Heart Neural Networks Field (AHNN Field) in addition to Artificial Neuron. This work takes its inspiration from both Heart and Brain
The Influence of Phosphorus- and Nitrogen- Containing Groups on the Thermal Stability and Combustion Characteristics of Styrenic Polymers
The effects of covalently bound phosphorus (P-) and nitrogen (N-) bearing groups on the thermal and combustion attributes of polystyrene have been investigated. The necessary chemical modifications were achieved through co- and ter-polymerisation reactions, in a suitable solvent, under radical initiation conditions. The influence of PâN cooperative interactions on the combustion properties of styrenic polymers was studied. The co-monomers of interest included: diethyl(acryloyloxymethyl)phosphonate (DEAMP), diethyl-p-vinylbenzylphosphonate (DEpVBP), acrylic acid-2-[(diethoxyphosphoryl)methyl amino]ethyl ester (ADEPMAE) and maleimide (MI). For the first time, the ter-polymers of styrene containing both P- groups, DEAMP or DEpVBP, and N- groups, MI, were prepared via solution polymerisation. It was found that the thermal stability and combustion characteristics of polystyrene were significantly altered by the presence of nominal amounts of P- and N- containing groups, and, in certain cases, cooperative interactions of these groups were also evident. For instance, the extents of char formation post-degradation of the prepared ter-polymers, as revealed by thermogravimetric investigations in an inert atmosphere (nitrogen), were found to be enhanced by more than 20%, as compared to the unmodified polystyrene. The heat release rates and heat release capacities of the ter-polymers, as measured using the pyrolysis combustion flow calorimetric (PCFC) technique, were reduced by almost 50% in comparison to the same parameters obtained for the unmodified counterpart
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Gaseous- and Condensed-Phase Activities of Some Reactive P- and N-Containing Fire Retardants in Polystyrenes
Polystyrene (PS) was modified by covalently binding P-, P-N- and/or N- containing fire-retardant moieties through co- or ter-polymerization reactions of styrene with diethyl(acryloyloxymethyl)phosphonate (DEAMP), diethyl-p-vinylbenzyl phosphonate (DEpVBP), acrylic acid-2-[(diethoxyphosphoryl)methylamino]ethyl ester (ADEPMAE) and maleimide (MI). In the present study, the condensed-phase and the gaseous-phase activities of the abovementioned fire retardants within the prepared co- and ter-polymers were evaluated for the first time. PyrolysisâGas Chromatography/Mass Spectrometry was employed to identify the volatile products formed during the thermal decomposition of the modified polymers. Benzaldehyde, α-methylstyrene, acetophenone, triethyl phosphate and styrene (monomer, dimer and trimer) were detected in the gaseous phase following the thermal cracking of fire-retardant groups and through main chain scissions. In the case of PS modified with ADEPMAE, the evolution of pyrolysis gases was suppressed by possible inhibitory actions of triethyl phosphate in the gaseous phase. The reactive modification of PS by simultaneously incorporating P- (DEAMP or DEpVBP) and N- (MI) monomeric units, in the chains of ter-polymers, resulted in a predominantly condensed-phase mode of action owing to synergistic P and N interactions. The solid-state 31P NMR spectroscopy, Scanning Electron Microscopy/Energy Dispersive Spectroscopy, Inductively-Coupled Plasma/Optical Emission Spectroscopy and X-ray Photoelectron Spectroscopy of char residues, obtained from ter-polymers, confirmed the retention of the phosphorus species in their structures
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Gaseous- and Condensed-Phase Activities of Some Reactive P- and N-Containing Fire Retardants in Polystyrenes
Polystyrene (PS) was modified by covalently binding P-, P-N- and/or N- containing fire-retardant moieties through co- or ter-polymerization reactions of styrene with diethyl(acryloyloxymethyl)phosphonate (DEAMP), diethyl-p-vinylbenzyl phosphonate (DEpVBP), acrylic acid-2-[(diethoxyphosphoryl)methylamino]ethyl ester (ADEPMAE) and maleimide (MI). In the present study, the condensed-phase and the gaseous-phase activities of the abovementioned fire retardants within the prepared co- and ter-polymers were evaluated for the first time. PyrolysisâGas Chromatography/Mass Spectrometry was employed to identify the volatile products formed during the thermal decomposition of the modified polymers. Benzaldehyde, α-methylstyrene, acetophenone, triethyl phosphate and styrene (monomer, dimer and trimer) were detected in the gaseous phase following the thermal cracking of fire-retardant groups and through main chain scissions. In the case of PS modified with ADEPMAE, the evolution of pyrolysis gases was suppressed by possible inhibitory actions of triethyl phosphate in the gaseous phase. The reactive modification of PS by simultaneously incorporating P- (DEAMP or DEpVBP) and N- (MI) monomeric units, in the chains of ter-polymers, resulted in a predominantly condensed-phase mode of action owing to synergistic P and N interactions. The solid-state 31P NMR spectroscopy, Scanning Electron Microscopy/Energy Dispersive Spectroscopy, Inductively-Coupled Plasma/Optical Emission Spectroscopy and X-ray Photoelectron Spectroscopy of char residues, obtained from ter-polymers, confirmed the retention of the phosphorus species in their structures