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Abstract

The possibility of the application of nontraditional method of greenhouse gas utilization by the injection of CO2 (sequestration) into porous geological deposits, treated as unconventional gas collectors, requires the fulfillment of basic criteria such as the impact on the environment and long term storage. The important issue is the physical behavior of the deposit during the porous structure saturation phase by carbon dioxide. What should be mentioned first and foremost is: the availability of CO2 transport along the porous structure and adsorption capacity. The work presents the results of water vapor sorption on coal samples from selected Hard Coal Mines of a differentiated carbon content. The received results were presented in the form of sorption and desorption isotherms performed in a temperature of 303 K. It was additionally described with a BET adsorption isotherm. Based on sorption data, a specific surface area was calculated, in accordance with BET theory. The amount of the adsorbed water vapor molecules for the analyzed coal samples was dependent on the degree of metamorphism. The obtained isotherms can be described as type II according to the BET classification. Volumetric type apparatus -adsorption- microburette liquid was used for the sorption experiments. Water vapor sorption in relation to coals allows for the quantitative determination of primary adsorption centers as a measure of adsorbed molecule interconnections with the adsorbent surface. Based on the BET adsorption equation, out of water vapor isotherms, the amount of adsorption active centers, which potentially may take part in CO2 adsorption in coal seams during injection of this gas, was determined. The sorption capacity of coals is determined by the degree of metamorphism, which also has very large impact on the sorption capacity of the deposit.

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Authors and Affiliations

Agnieszka Orzechowska-Zięba
Paweł Baran
Katarzyna Zarębska
Janusz Cygankiewicz
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Abstract

It is estimated that the amount of used car tires in the European Union in 2016 was established at the level of 3,515,000 Mg, which is undoubtedly a problem from the point of view of engineering and environmental protection. An alternative to storing this waste in landfills is their pyrolysis. As a result of thermal decomposition, calorific value products (oil and gas fraction) are obtained, as well as a solid residue, which due to its composition and properties can be processed into a high quality carbon sorbent. For this purpose, various methods of modification of the pyrolyzate are used, both involving physical and chemical activation. This article presents the characteristics of solid residue after the pyrolysis of rubber tires running at a temperature of about 400°C, which included an analysis of chemical composition (XRF and IR), mineralogical composition (XRD, SEM-EDS) and textural characteristics. Additionally, for the purpose of activation, the sample was treated with nitrogen at a temperature of 550°C. The mineralogical analysis showed that the dominant mineral component is carbon. In addition, the presence of quartz, calcite and sphalerite was observed. Analysis of the chemical composition suggests that due to the high carbon content (about 80% by mass) it is possible for a carbon sorbent from the analyzed waste to be obtained. However, previous preliminary studies did not allow a material constituting a substitute for activated carbon to be obtained, because the applied modification only slightly increased the BET specific surface area, which reached the value of approx. 85 m2/g. Based on the analysis of the pore size distribution of the 2 tested samples, it was found to be homogeneous/modal with a micro/mesoporous nature, while the shape of the hysteresis loop suggests the presence of “bottle shape” pores. Due to the relatively high content of zinc, the composition of waste (about 4% of mass), the possibility of recovery of this element should also be considered.

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Authors and Affiliations

Dorota Czarna-Juszkiewicz
Magdalena Wdowin
Piotr Kunecki
Paweł Baran
Rafał Panek
Robert Żmuda

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