Micro-Calorimetric Study on the Thermal Stability of N, N-Dimethylhydroxylamine in the APOR Process

2019 ◽  
Vol 5 (2) ◽  
Author(s):  
Cao Zhi ◽  
Yan Taihong ◽  
Bian Xiaoyan ◽  
Li Chuanbo ◽  
Zuo Chen ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Fission Products ◽  
Decomposition Temperature ◽  
Nitrogen Atmosphere ◽  
Molar Enthalpy ◽  
Enthalpies Of Formation ◽  
Initial Reaction ◽  
Calorimetric Study ◽  
Hno3 Solution ◽  
Thermal Stability Of

The thermal stability of N, N-dimethylhydroxylamine (DMHAN) in the HNO3 solution was studied using microcalorimeter. The influence of concentration of HNO3, DMHAN, methylhydrazine (MH), atmosphere (air and nitrogen), and metals was investigated. The kinetic parameters and self-accelerating decomposition temperature (SADT) of the feed in process (stripping reagents 1BX, scouring agent 2DS, stripping reagents 2BX, and waste aqueous phase 2DW) were calculated by Advanced Kinetics and Technology Solutions (akts) thermokinetics software. The molar enthalpy of the reaction of NaNO2 with DMHAN and MH was also determined. The results show that the initial reaction temperature (T0) of DMHAN/HNO3 (HNO3: 1.5–3.0 mol/L, DMHAN: 0.05–0.8 mol/L) is increased as the acidity is reduced or the concentration of DMHAN is increased. Holding reductant MH made the induction period of the autocatalytic reaction longer. The air, nitrogen atmosphere, Fe, and the fission products (Zr, Ru) do not affect the decomposition of DMHAN, but the stainless steel made the T0 of DMHAN/HNO3 become lower. The SADT of 1BX/2DS, 2BX, and 2DW is 56 °C, 52 °C and 47 °C, respectively. The molar enthalpies of formation of the reaction of NaNO2 with DMHAN and MH are −411.3 kJ/mol, −246.0 kJ/mol, respectively.

Non-Isothermal Decomposition Kinetic of Polypropylene/Hydrotalcite Composite

2019 ◽  
Vol 19 (11) ◽  
pp. 7493-7501 ◽  
Author(s):  
Sheng Xu ◽  
Min Zhang ◽  
Siyu Li ◽  
Moyu Yi ◽  
Shigen Shen ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Thermal Decomposition ◽  
Nitrogen Atmosphere ◽  
Heating Rates ◽  
Decomposition Reactions ◽  
Kinetic And Thermodynamic Parameters ◽  
Málek Method ◽  
Boundary Reaction ◽  
Phase Boundary Reaction ◽  
Thermal Stability Of

P3O5-10 pillared Mg/Al hydrotalcite (HTs) as a functional fire-retarding filler was successfully prepared by impregnation-reconstruction, where the HTs was used to prepare polypropylene (PP) and HTs composite (PP/HTs). Thermal decomposition was crucial for correctly identifying the thermal behavior for the PP/HTs, and studied using thermogravimetry (TG) at different heating rates. Based on single TG curves and Málek method, as well as 41 mechanism functions, the thermal decompositions of the PP/HTs composite and PP in nitrogen atmosphere were studied under non-isothermal conditions. The mechanism functions of the thermal decomposition reactions for the PP/HTs composite and PP were separately “chemical reaction F3” and “phase boundary reaction R2,” which were also in good agreement with corresponding experimental data. It was found that the addition of the HTs increased the apparent activation energy Ea of the PP/HTs comparing to the PP, which improved the thermal stability of the polypropylene. A difference in the set of kinetic and thermodynamic parameters was also observed between the PP/HTs and PP, particularly with respect to lower ΔS≠ value assigned to higher thermal stability of the PP/HTs composite.

scholarly journals The Thermal Properties of Polyurethane/Neoprene Blends on Prosthetic Foot

2020 ◽  
Vol 990 ◽  
pp. 106-110
Author(s):  
Mohd Zulkifli Mohamad Noor ◽  
Mohamad Anas Mohd Azmi ◽  
Mohd Shaiful Zaidi Mad Desa ◽  
Mohd Bijarimi Mat Piah ◽  
Azizan Ramli
Keyword(s):  
Thermal Stability ◽  
Thermal Properties ◽  
Low Cost ◽  
Decomposition Temperature ◽  
Gravimetric Analysis ◽  
Thermal Gravimetric ◽  
Prosthetic Foot ◽  
Reinforced Polymer ◽  
New Material ◽  
Thermal Stability Of

Neoprene reinforced polymer has become an attraction in current research and development of new material blend. In this invention, neoprene was chosen to be enhance to polyurethane because of their superior properties that possess extraordinary mechanical, electrical, optical and thermal properties on prosthetic foot. In this research, polyurethane was chosen due to good rigidity, easy processing and low cost. The reinforcement polyurethane with neoprene is expected to improve the properties of polyurethane. The objective of this research was conducted to investigate the effect of neoprene contents on thermal properties of polyurethane reinforced neoprene on prosthetic foot. The effect of neoprene on thermal properties neoprene reinforced polyurethane was analysed in term of its thermal stability by thermal gravimetric analysis (TGA). Moreover, the visual of small topographic details on the surface of polyurethane/neoprene blends will be examined by scanning electron microscope (SEM). Based on result, the thermal properties show the great enhancement at high neoprene contents which is 1.0wt%. The thermal stability of polyurethane reinforced neoprene improves when the temperature where decomposition starts to occurs are higher than decomposition temperature of pure polyurethane. Then, thermal conductivity of polyurethane shows the great improvement after the addition of neoprene. Lastly, the smooth surface and visible of sheets pattern on surface represent the present of neoprene disperse into polymer that enhance brittleness. Thus, the presence of neoprene has clearly enhanced the thermal stability of the polyurethane. Table 1 shows formulation of neoprene and polyurethane.

The reactivity of bentonites: a review. An application to clay barrier stability for nuclear waste storage

Clay Minerals ◽  
1998 ◽  
Vol 33 (2) ◽  
pp. 187-196 ◽  
Author(s):  
A. Meunier ◽  
B. Velde ◽  
L. Griffault
Keyword(s):  
Thermal Stability ◽  
Nuclear Waste ◽  
Mineral Assemblage ◽  
Hydrothermal Systems ◽  
Initial Reaction ◽  
Nuclear Waste Storage ◽  
Waste Storage ◽  
Kinetics Of ◽  
Clay Barrier ◽  
Thermal Stability Of

AbstractThe thermal stability of bentonites is of particular interest for containment barriers in nuclear waste storage facilities. The kinetics of smectite reactions have been investigated under laboratory conditions for some time. The variables of time, chemical composition and temperature have been varied in these experiments. The results of such an assessment are that there are about as many kinetic values deduced from experiments as there are experiments.Experiments using natural bentonite to study the smectite-to-illite conversion have been interpreted as a progressive transformation of montmorillonite to illite. It is highly probable that the initial reaction product is not illite but a high-charge beidellite + saponite + quartz mineral assemblage which gives, then, beidellite-mica interstratified mixed-layer minerals. These experimental reactions are noticeably different from those of diagenesis, being closer to reactions in hydrothermal systems.

Studies on Thermal Stability and Rheological Property of PU/PVDF Blend

2011 ◽  
Vol 311-313 ◽  
pp. 1065-1070
Author(s):  
Guo Lan Huan ◽  
Jian Li Liu ◽  
Qi Yun Du ◽  
Xiao Yu Hu
Keyword(s):  
Activation Energy ◽  
Thermal Stability ◽  
Thermal Decomposition ◽  
Shear Stress ◽  
Rheological Property ◽  
Decomposition Temperature ◽  
Dynamic Equations ◽  
Thermal Decomposition Temperature ◽  
Thermal Stability Of ◽  
Decomposition Activation Energy

In this article, the thermal stability of PU/PVDF blend was investigated by thermogravimetry (TG), and their rheological property was studied through testing and analyzing the rheological curves. The results showed that, with the increase in PVDF content, the thermal decomposition temperature of PU/PVDF blend increased, and by fitting relevant data to thermal decomposition dynamic equations, it was found that thermal decomposition activation energy of the blend increased gradually, i.e. the thermal stability of the blend increased gradually. Meantime, based on the curves of shear stress vs. shear rate of the blend at 180°C and 200°C, it was shown that for PU/PVDF blend, with the decrease of temperature and the increase in PVDF content, the non-Newtonian index decreased, while the viscosity of the blend increased.

Thermal Degradation Study of Functionalized MWNT Reinforced Segmented Polyurethane Membrane

2006 ◽  
Vol 38 (3) ◽  
pp. 261-271 ◽  
Author(s):  
S. Mondal ◽  
J. L. Hu
Keyword(s):  
Thermal Stability ◽  
Thermal Degradation ◽  
Nitrogen Atmosphere ◽  
Segmented Polyurethane ◽  
Degradation Study ◽  
Heat Treated ◽  
Different Temperatures ◽  
Increasing Temperature ◽  
Thermal Stability Of ◽  
Mwnt Content

The thermal degradation of polytetramethylene glycol (PTMG, Mn 1/42900) based polyurethane (PU), along with four different weight contents (such as 0.25, 0.50, 1.0, and 2.5 wt%) of functionalized multiwalled nanotube (MWNT) reinforced PUs are studied in air as well as in nitrogen atmosphere. The degradation results are reported in 10 and 50% weight loss and derivative of thermogravimetry (DTG). As expected, PUs are thermally more stable in nitrogen than in air. However, the influence of MWNT content on thermal stability is unclear. At 0.25 and 0.50 wt% of MWNT content, thermal stability declined and a further increase of MWNT improved the thermal stability of PU. Fourier-transform infrared (FTIR) analysis is also performed for untreated and heat treated films in order to understand the degradation at different temperatures. Free C1/4O stretching neck dimension increases with increasing temperature which signifies breaking of H-bonding detected by FTIR measure ments.

scholarly journals Stable Organic-Inorganic Hybrid Bismuth-Halide Monocrystalline Compounds With Adjustable Optoelectronic Properties

2021 ◽  
Author(s):  
Xinru Hu ◽  
Jilin Wang ◽  
Jian He ◽  
Guoyuan Zheng ◽  
Disheng Yao ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Room Temperature ◽  
Diffuse Reflectance ◽  
Decomposition Temperature ◽  
X Ray Diffraction ◽  
Monoclinic System ◽  
X Ray ◽  
Good Thermal Stability ◽  
Chemical Groups ◽  
Thermal Stability Of

Abstract Two kinds of novel organic-inorganic bismuth-halide hybrid monocrystalline compounds (C6H5CH2NH3)2BiCl5 and (C6H5CH2NH3)BiI4 were synthesized and characterized. The crystal structure, intermolecular interaction, morphology, chemical groups and bonds, optical and thermal stability of the samples were systematically investigated through single crystal X-ray diffraction, Hirshfeld surface analysis, SEM, FTIR, TG and UV-vis diffuse reflectance spectra. The results indicated that (C6H5CH2NH3)2BiCl5 and (C6H5CH2NH3)BiI4 crystals displayed a monoclinic system with the space group P21/c and P21/n at room temperature, respectively. These materials showed strong absorption in the ultraviolet and visible light regions, resulting in very low Eg, which could be continuously adjustable from 1.67 eV to 3.21 eV by changing the halogen ratio. In addition, these hybrid materials also exhibited good thermal stability. The decomposition temperature of (C6H5CH2NH3)2BiCl5 and (C6H5CH2NH3)BiI4 were 260℃ and 300℃ respectively. Therefore, these organic-inorganic bismuth-halide hybrid compounds have excellent development potential in the field of solar cell research.

Thermal Stability of FeS2 Cathode Material in “Thermal” Batteries: Effect of Dissolved Oxides in Molten Salt Electrolytes

2008 ◽  
Vol 63 (9) ◽  
pp. 596-602 ◽  
Author(s):  
Patrick J. Masset
Keyword(s):  
Thermal Stability ◽  
Liquid Phase ◽  
Cathode Material ◽  
Molten Salt ◽  
Molten Salts ◽  
Decomposition Temperature ◽  
Lithium Oxide ◽  
Thermal Batteries ◽  
Molten Salt Electrolytes ◽  
Thermal Stability Of

The thermal stability of FeS2 cathode material for thermal batteries is investigated in the LiCl-KCl eutectic containing up to 10 wt% Li2O (used as anti-peak). The results show that the decomposition of pyrite shifts to higher temperatures in the presence of molten salts as the S2 gas is repressed by the liquid phase. For high lithium oxide contents the decomposition temperature of pyrite decreases by 100 °C. In addition Li2FeS2 as reaction product is evidenced whereas Li3Fe2S4 is expected from literature data.

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