scholarly journals Thermal decomposition characteristics of foundry sand for cast iron in nitrogen atmosphere

2018 ◽  
Vol 5 (12) ◽  
pp. 181091 ◽  
Author(s):  
Qingwei Xu ◽  
Kaili Xu ◽  
Xiwen Yao ◽  
Jishuo Li ◽  
Li Li
Keyword(s):  
Activation Energy ◽  
Thermal Decomposition ◽  
Cast Iron ◽  
Low Cost ◽  
Temperature Stability ◽  
Nitrogen Atmosphere ◽  
High Temperature Stability ◽  
Kinetics Parameters ◽  
Foundry Sand ◽  
Exponential Factor

Sand casting, currently the most popular approach to the casting production, has wide adaptability and low cost. The thermal decomposition characteristics of foundry sand for cast iron were determined for the first time in this study. Thermogravimetry was monitored by simultaneous thermal analyser to find that there was no obvious oxidation or combustion reaction in the foundry sand; the thermal decomposition degree increased as the heating rate increased. There was an obvious endothermic peak at about 846 K due to the transition of quartz from β to α phase. A novel technique was established to calculate the starting temperature of volatile emission in determining the volatile release parameter of foundry sand for cast iron. Foundry sand does not readily evaporate because its volatile content is only about 2.68 wt% and its main components have high-temperature stability. The thermal decomposition kinetics parameters of foundry sand, namely activation energy and pre-exponential factor, were obtained under kinetics theory. The activation energy of foundry sand for cast iron was small, mainly due to the wide temperature range of thermal decomposition in the foundry sand.

scholarly journals Kinetic Parameters for the Thermal Decomposition of Forest Waste Using Distributed Activation Energy Model (DAEM)

2017 ◽  
Vol 19 (1) ◽  
pp. 15-32 ◽  
Author(s):  
Alok Dhaundiyal ◽  
Pramod Tewari
Keyword(s):  
Experimental Data ◽  
Activation Energy ◽  
Thermal Decomposition ◽  
Asymptotic Expansion ◽  
Nitrogen Atmosphere ◽  
Energy Model ◽  
Pine Needle ◽  
Distributed Activation Energy Model ◽  
Exponential Factor ◽  
Forest Waste

Abstract The purview of paper pivoted around the pyrolysis decomposition of forest waste (pine needle litter) by thermogravimetric analysis (TGA). Experiments were carried out in the presence of Nitrogen atmosphere. The experimental data was compared with those obtained by numerical solution of distributed activation energy model (DAEM). Asymptotic expansion is adopted to evaluate the pre-exponential factor, mean activation energy and variance. The correction factor Bi has been invoked to describe accurately the differential thermogravitmeric curves of thermal decomposition of pine needles.

scholarly journals Thermal Decomposition of 3-Nitro-1,2,4-Triazole-5-One (NTO) and Nanosize NTO Catalyzed by NiFe2O4

2022 ◽  
Author(s):  
Pragnesh N. Dave ◽  
Ruksana Sirach ◽  
Riddhi Thakkar ◽  
Shalini Chaturvedi
Keyword(s):  
Activation Energy ◽  
Thermal Decomposition ◽  
Catalytic Activity ◽  
Nickel Catalyst ◽  
Nickel Ferrite ◽  
Peak Temperature ◽  
Kinetics Parameters ◽  
Exponential Factor ◽  
Nanometer Size ◽  
Co Precipitation

Abstract Nanosize Nickel ferrite (NiF) was synthesized by the co-precipitation methods and its effect as a 5 % by mass additive was studied on the thermal decomposition of micrometer and nanometer size NTO. In the presence of 5 % NiF additive, the thermal decomposition peak temperature of NTO was decreased from 276.36 to 260.18 oC and that of nano NTO was decreased from 261.38 to 258.89 oC (β=10 oC min-1). The kinetics parameters confirms the catalytic activity of NiF for the thermal decomposition of NTO, and nNTO as the parameters such as activation energy (NTO=~25.45 % and nNTO=~45.94 % decrement), and pre-exponential factor (NTO=~21.94 % and nNTO=~43.12 % decrement) were decreased when 5 % NiF additive was added to NTO, and nNTO. The rate of the decomposition process was increased in the presence of 5 % NiF catalyst, indicating the faster thermal decomposition of both NTO, and nNTO in the presence of nickel catalyst.

Application of Calculus Equation in Solving Thermal Decomposition Kinetics Parameters of Flame Retardant Wood

2014 ◽  
Vol 983 ◽  
pp. 190-193
Author(s):  
Cai Yun Sun ◽  
Yong Li Yang ◽  
Ming Gao
Keyword(s):  
Activation Energy ◽  
Thermal Decomposition ◽  
Thermal Degradation ◽  
Phosphoric Acid ◽  
Flame Retardant ◽  
Kinetic Parameters ◽  
Flame Retardancy ◽  
Decomposition Kinetics ◽  
Thermal Decomposition Kinetics ◽  
Kinetics Parameters

Wood has been treated with amino resins and amino resins modified with phosphoric acid to impart flame retardancy. The thermal degradation of samples has been studied by thermogravimetry (TG) in air. From the resulting data, kinetic parameters for different stages of thermal degradation are obtained following the method of Broido. For the decomposition of wood and flame retardant wood, the activation energy is found to decrease from 122 to 72 kJmol-1.

scholarly journals THE KINETICS OF CaO ASSISTED PATTUKKU CHARCOAL STEAM GASIFICATION

REAKTOR ◽  
2018 ◽  
Vol 18 (1) ◽  
pp. 16
Author(s):  
Takdir Syarif ◽  
H Sulistyo ◽  
Wahyudi B Sediawan ◽  
B Budhijanto
Keyword(s):  
Activation Energy ◽  
Tubular Reactor ◽  
Steam Gasification ◽  
Effect Of Temperature ◽  
Composition Analysis ◽  
Zone Model ◽  
Kinetics Parameters ◽  
Exponential Factor ◽  
Surface Diffusivity ◽  
Gasification Process

Abstract Coal is a solid fuel that can be converted into syngas through gasification process. To obtain optimum gasification process design and operation, in-depth understanding of the influential parameters is required. This study aims to investigate the effect of temperature on the gasification process and to obtain its kinetics parameters. The study was carried out in a tubular reactor equipped with a heater and a condenser. Steam was used as gasifying agent, while CaO was employed as a CO2 adsorbent. The charcoal from coal was subjected to gasification at temperatures of 600°C, 700°C, and 800°C. The ratio of charcoal and CaO was 1:1. The gasification process lasted for 60 minutes with gas sample was taken every 15 minutes for composition analysis. The results showed that a temperature increase of 100°C caused a proportional increase of conversion of about 75% higher. The value of activation energy (Ea) and exponential factor (ko) were 46.645kJ/mole and 328.3894/min, respectively. For mass transfer parameters, values of activation energy for surface diffusion (Es) and surface diffusivity factor (as) were 81.126 kJ/mole and 0.138/min, respectively. Keywords: gasification; mathematical model; Pattukku coal char; steam; Thin Reaction Zone Model

Studies on the Thermal Decomposition Kinetic of an Nitrate Ester

2012 ◽  
Vol 182-183 ◽  
pp. 1575-1580 ◽  
Author(s):  
Juan Wang ◽  
Da Bin Liu ◽  
Xin Li Zhou
Keyword(s):  
Activation Energy ◽  
Thermal Decomposition ◽  
Decomposition Mechanism ◽  
Thermal Decomposition Mechanism ◽  
Decomposition Kinetic ◽  
Heating Rates ◽  
Exponential Factor ◽  
Nitrate Ester ◽  
Dynamic Function ◽  
Thermal Decomposition Kinetic

The certain nitrate ester explosive has been tested by TG at the heating rates of 10, 15, 20, 25K•min-1. Basing on the TG experiment results the thermal decomposition activation energy has been calculated by the methods of Ozawa, KAS and iteration. And the thermal decomposition mechanism function of the explosive with 38 kinds of dynamic function was deduced by the method of integration. The results show that the thermal decomposition mechanism of the nitrate ester is chemical reaction mechanism. The thermal decomposition kinetic parameters such as average activation energy Ea and pre-exponential factor A are 133.23×103 J•mol-1 and 3.191×107 s-1 respectively.

scholarly journals Materials and Applications for Low-Cost Ceramic Membranes

Membranes ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 105 ◽  
Author(s):  
Amanmyrat Abdullayev ◽  
Maged Bekheet ◽  
Dorian Hanaor ◽  
Aleksander Gurlo
Keyword(s):  
Water Treatment ◽  
Raw Materials ◽  
Low Cost ◽  
Temperature Stability ◽  
Ceramic Membranes ◽  
Production Costs ◽  
High Temperature Stability ◽  
Waste Products ◽  
Recent Developments ◽  
Materials Used

In water treatment applications, the use of ceramic membranes is associated with numerous advantages relative to polymer-based filtration systems. High-temperature stability, fouling resistance, and low maintenance requirements contribute to lower lifecycle costs in such systems. However, the high production costs of most commercially available ceramic membranes, stemming from raw materials and processing, are uneconomical for such systems in most water treatment applications. For this reason, there is a growing demand for new ceramic membranes based on low-cost raw materials and processes. The use of unrefined mineral feedstocks, clays, cement, sands, and ash as the basis for the fabrication of ceramic membranes offers a promising pathway towards the obtainment of effective filtration systems that can be economically implemented in large volumes. The design of effective ceramic filtration membranes based on low-cost raw materials and energy-efficient processes requires a balance of pore structure, mass flow, and robustness, all of which are highly dependent on the composition of materials used, the inclusion of various pore-forming and binding additives, and the thermal treatments to which membranes are subjected. In this review, we present recent developments in materials and processes for the fabrication of low-cost membranes from unrefined raw materials, including clays, zeolites, apatite, waste products, including fly ash and rice husk ash, and cement. We examine multiple aspects of materials design and address the challenges relating to their further development.

Thermal Cure and Ceramization Kinetics of Perhydropolysilazane

2013 ◽  
Vol 575-576 ◽  
pp. 81-86 ◽  
Author(s):  
Feng Ling Ma ◽  
Hui Min Qi ◽  
Ya Ping Zhu ◽  
Xiao Wen Ren ◽  
Fan Wang
Keyword(s):  
Activation Energy ◽  
Weight Loss ◽  
Thermogravimetric Analysis ◽  
Kinetic Parameters ◽  
Nitrogen Atmosphere ◽  
Thermal Cure ◽  
Exponential Factor ◽  
Kinetics Of

The kinetics of the thermal cure and ceramization of preceramic prehydropolysilazane (PHPS) was investigated by thermogravimetric analysis (TGA) under nitrogen atmosphere. The results indicated that the gases captured during the thermal cure and ceramization process of PHPS, which had three main weight loss events. The corresponding kinetic parameters including activation energy, pre-exponential factor and empirical order of the thermal cure and ceramization stages were evaluated by using Ozawa and Kissinger metnods, respectively.

The Influence of Degree of Polymerization on Precursor-Derived Si-B-C-N Ceramics

2010 ◽  
Vol 650 ◽  
pp. 355-360
Author(s):  
Xiang Geng ◽  
X. Huang ◽  
Ya Jing Li ◽  
Song Li ◽  
Xiao Bin Shi
Keyword(s):  
High Temperature ◽  
Solid State ◽  
Amorphous Materials ◽  
Chemical Properties ◽  
Temperature Stability ◽  
High Hardness ◽  
Nitrogen Atmosphere ◽  
Degree Of Polymerization ◽  
Pyrolysis Process ◽  
High Temperature Stability

Precursor derived Si-B-C-N ceramic is a kind of amorphous materials with high hardness, low density, durability at extremely high temperature. The materials show a great potential to be used in the field of the Thermal Protective System (TPS). The physical states and chemical properties of the amorphous materials greatly depend on the starting materials. The effect of degree of polymerization (DP) of the precursor on the pyrolysis process and the characteristics of the amorphous Si-B-C-N materials are studied. The SiBCN-based preceramic polymer synthesized by dichloromethylvinylsilane, ammonia and BH3•SMe2. Dichloromethylvinylsilane reacted with ammonia and BH3•SMe2 in toluene or tetrahydrofuran (THF) as solvent in the presence of catalytic amounts of pyridine. The polymeric precursors were cured at low temperature to obtain solid-state precursors. Pyrolysis process of the solid-state precursors under various temperatures and carried out in nitrogen atmosphere. The results showed that DP of the precursor influences the pyrolysis process and the high temperature stability of the Si-B-C-N amorphous ceramics.

scholarly journals Thermal decomposition kinetics of raw and treated olive waste

2019 ◽  
Vol 23 (6 Part A) ◽  
pp. 3501-3512
Author(s):  
Zhihong Wang ◽  
Chengzhang Wang ◽  
Mijun Peng
Keyword(s):  
Activation Energy ◽  
Thermal Decomposition ◽  
Thermodynamic Characteristics ◽  
Nitrogen Atmosphere ◽  
Enzyme Hydrolysis ◽  
Conversion Degree ◽  
Thermal Decomposition Mechanism ◽  
Scanning Calorimetry ◽  
Two Samples ◽  
Olive Waste

The pyrolysis characteristic of raw and ultrasound assisted enzyme hydrolysis treated (UAEH) olive waste was investigated using the thermogravimetric analysis at 5, 10, 15, and 20?C per minute in the nitrogen atmosphere. The thermal decomposition was divided into three stages in the thermograph curve, and the thermogravimetric curve showed the same decomposition trend for two samples. The temperature interval and peak temperature were different for two different samples, and moved to higher temperature with the increase in heating rate. Differential thermogravimetric and differential scanning calorimetry curves depicted that the structure and composition of samples were changed by UAEH. Meanwhile, the kinetic parameters were calculated by the Kissinger, Kissinger-Akahira-Sunose, Flynn-Wall-Ozawa, and Coats-Redfern methods. For untreated and treated olive waste, the Kissinger-Akahira-Sunose and Flynn-Wall-Ozawa methods revealed the similar kinetic characteristics for the conversion degree from 0.1 to 0.9, and the average values of activation energy were 201.42 kJ/mol and 162.97 kJ/mol, respectively. The change in activation energy was clearly dependent on the extent of conversion. The Coats-Redfern method suggested the second-order model (F2, f(?) = (1 ? ?)2) could be used to better describe the thermal decomposition mechanism of untreated and treated olive waste. Besides, thermodynamic characteristics of olive waste treated were consistent with that of the untreated sample.

Preparation of Anhydrous Magnesium Chloride from MgCl2·6H2O Ⅱ Thermal Decomposition Mechanism of the Intermediate Product

2005 ◽  
Vol 488-489 ◽  
pp. 61-64 ◽  
Author(s):  
Xing Fu Song ◽  
Jin Wang ◽  
Xiang Tian Wang ◽  
Jian Guo Yu
Keyword(s):  
Thermal Decomposition ◽  
Magnesium Chloride ◽  
Decomposition Process ◽  
Isothermal Kinetics ◽  
Thermal Decomposition Mechanism ◽  
Kinetics Parameters ◽  
Exponential Factor ◽  
Anhydrous Magnesium Chloride ◽  
Three Stages ◽  
Kinetics Of

Magnesium chloride hex-ammoniate (MgCl2·6NH3) is an intermediate to produce anhydrous magnesium chloride (MgCl2) by method of reaction crystallization. MgCl2·6NH3 is decomposed at 670K to produce anhydrous magnesium chloride. The process of thermal decomposition and its non-isothermal kinetics of MgCl2·6NH3 is studied. Results show that the thermal decomposition process is made up of three stages, the thermal decomposition functions and the thermal decomposition kinetics parameters, such as activation energy (E), pro-exponential factor (A) of MgCl2·6NH3 for each step are obtained by means of the Acher differential, the Coats-Redfern integral and multi-accelerated heating rate method. This study provides a valuable theoretical basis for MgCl2·6NH3 decomposition process on industrialization.

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