Thermokinetic behaviour and functional group variation during spontaneous combustion of raw coal and its preoxidised form.

Coal spontaneous combustion (CSC) is a major problem in coal mining. In the vicinity of underground goaf, secondary or repeated oxidation processes of the residual coal inevitably occur, increasing the risk of coal fires. In this study, the thermal reaction behaviour of two types of raw coal samples and three preoxidised coal samples with different oxidation temperatures (80, 130, and 180 °C) were investigated. The physical and chemical properties of the samples were measured using thermogravimetric analyser-Fourier transform infrared spectroscopy (TGA-FTIR) with heating rates of 1.0, 2.0, 5.0, and 10.0 °C min-1. According to the characteristic temperatures in the heating processes, the entire CSC procedure can be divided into three stages: oxidation, combustion, and burnout. The results indicated that the aliphatic side chain lengths of preoxidised coal were shorter, and the number of branched aliphatic side chains was lower than that of raw coal. Furthermore, the model for the mechanism of preoxidised coal differed from that of raw coal. Average values of the apparent activation energy of the preoxidised coal samples were lower than those of the raw coal samples. Therefore, compared with raw coal, preoxidised coal requires less energy to react and more readily undergoes spontaneous combustion.

Thermal hazards of benzoyl peroxide and its derived process products through theoretical thermodynamics assessment and different calorimetric technologies.

Benzoyl peroxide (BPO) is one of the primary OPs used as an initiator, curing agent, or medicine. Some of the plastic processes use BPO without air for maintaining the efficiency of the entire reaction. However, there have been numerous accidents involving BPO in petrochemical plants, especially those related to fire and explosion, that are due to its unstable thermal properties and peroxy bond (OO). BPO can be identified as a typical substance with autocatalytic reaction characteristics. Therefore, the related processes and their products are critical to prevent these kinds of chemical contingencies. This research was based on two types of instruments (nonisothermal and isothermal calorimetry), and theoretical methods to further determine the thermal hazard level. From the experimental results for BPO and BPO mixed with its by-products, the heat of decomposition was much higher (from 800 to 1235 J/g), the time to maximum rate under isothermal conditions was much shorter (from 99.1 to 17.4 h at 75.0 °C), and the apparent activation energy was much lower (from 118 to 91 kJ/mol) after BPO was mixed with its by-products. Therefore, the hazard level of BPO mixed with its by-products from the reaction process was much higher than that of pure BPO.

Effects of UV for Cycloaliphatic Epoxy Resin via Thermokinetic Models, Novel Calorimetric Technology, and Thermogravimetric Analysis.

The cycloaliphatic epoxy resin selected for this study was 3,4-epoxycyclohexane methyl-3'4'-epoxycyclohexyl-carboxylate (EEC). Epoxy resin has numerous applications, such as varnishes, tires, and electronic materials. However, the extensive used of chlorofluorocarbon (CFC) compounds in the last century has resulted in the formation of a hole in the ozone layer. As a consequence, solar radiation is intensifying gradually; therefore, continuous irradiation by sunlight should be avoided. The results of solar radiation can exacerbate the deterioration and photolysis of compounds. Through thermogravimetry and differential scanning calorimetry, the apparent onset temperature of EEC and EEC was analyzed under UV radiation for different durations. Thermokinetic data were used to determine the parameters of thermal decomposition characteristics through simulation to assess the reaction of EEC and EEC under UV radiation for different durations. The goal of the study was to establish the parameters of thermal decomposition characteristics for the effects of UV on EEC, as well as the probability of severity of thermal catastrophe.