Growing requirements in the field of environmental protection and waste management result in the need to search for new and effective methods of recycling various types of waste. From the perspective of technical and natural sciences, the disposal of hazardous waste, which can lead to environmental degradation, is of utmost importance. A particularly hazardous waste is asbestos, used until recently in many branches of the economy and industry. Despite the ban on the production and use of asbestos introduced in many countries, products containing it are still present in the environment and pose a real threat. This paper presents the results of research related to the process of asbestos neutralization, especially the chrysotile variety, by the thermal decomposition method. Changes in the mineralogical characteristics of asbestos waste were studied using the following methods: TG-DTA-EGA, XRD, SEM-EDS and XRF. The characteristics of the chrysotile asbestos sample were determined before and after thermal treatment at selected temperatures. The second part of the study focuses on the kinetic aspect of this process, where the chrysotile thermal decomposition process was measured by two techniques: ex situ and in situ. This study showed that the chrysotile structure collapsed at approximately 600–800 °C through dehydroxylation, and then the fibrous chrysotile asbestos was transformed into new mineral phases, such as forsterite and enstatite. The formation of forsterite was observed at temperatures below 1000 °C, while enstatite was created above this temperature. From the kinetic point of view, the chrysotile thermal decomposition process could be described by the Avrami–Erofeev model, and the calculated activation energy values were ~180 kJ mol−1 and ~220 kJ mol−1 for ex situ and in situ processes, respectively. The obtained results indicate that the thermal method can be successfully used to detoxify hazardous chrysotile asbestos fibers.

Kinetic Aspects of Chrysotile Asbestos Thermal Decomposition Process

Bloise, Andrea
2025-01-01

Abstract

Growing requirements in the field of environmental protection and waste management result in the need to search for new and effective methods of recycling various types of waste. From the perspective of technical and natural sciences, the disposal of hazardous waste, which can lead to environmental degradation, is of utmost importance. A particularly hazardous waste is asbestos, used until recently in many branches of the economy and industry. Despite the ban on the production and use of asbestos introduced in many countries, products containing it are still present in the environment and pose a real threat. This paper presents the results of research related to the process of asbestos neutralization, especially the chrysotile variety, by the thermal decomposition method. Changes in the mineralogical characteristics of asbestos waste were studied using the following methods: TG-DTA-EGA, XRD, SEM-EDS and XRF. The characteristics of the chrysotile asbestos sample were determined before and after thermal treatment at selected temperatures. The second part of the study focuses on the kinetic aspect of this process, where the chrysotile thermal decomposition process was measured by two techniques: ex situ and in situ. This study showed that the chrysotile structure collapsed at approximately 600–800 °C through dehydroxylation, and then the fibrous chrysotile asbestos was transformed into new mineral phases, such as forsterite and enstatite. The formation of forsterite was observed at temperatures below 1000 °C, while enstatite was created above this temperature. From the kinetic point of view, the chrysotile thermal decomposition process could be described by the Avrami–Erofeev model, and the calculated activation energy values were ~180 kJ mol−1 and ~220 kJ mol−1 for ex situ and in situ processes, respectively. The obtained results indicate that the thermal method can be successfully used to detoxify hazardous chrysotile asbestos fibers.
2025
chrysotile asbestos
dehydroxylation
kinetic
thermal decomposition
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11770/390619
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