Synthesis and Characterization of Iron-Rich Glass Ceramic Materials: A Model for Steel Industry Waste Reuse

被引:7
|
作者
Carlini, Riccardo [1 ]
Alfieri, Ilaria [2 ]
Zanicchi, Gilda [1 ]
Soggia, Francesco [1 ]
Gombia, Enos [3 ]
Lorenzi, Andrea [2 ]
机构
[1] Univ Genoa, Dept Chem & Ind Chem, Via Dodecaneso 31, I-16146 Genoa, Italy
[2] Univ Parma, Dept Chem, Parco Area Sci 17-A, I-43124 Parma, Italy
[3] IMEM CNR, Parco Area Sci 37-A, I-43124 Parma, Italy
关键词
Glass-ceramics; Electrical properties; Leaching tests; Iron rich waste; Vitrification; MOSSBAUER-SPECTROSCOPY; MAGNETIC-PROPERTIES; CORROSION BEHAVIOR; SLAG; REDUCTION; HEMATITE; PHASES;
D O I
10.1016/j.jmst.2016.09.008
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Wastes deriving from steel industry, containing large amounts of iron oxides and heavy metals, when collected in landfills are subjected to atmospheric agents, with consequent release of toxic substances in the soil and groundwater. The reuse of these wastes as raw materials for the production of advanced materials is a viable way both to overcome the environmental impact and to reduce the disposal costs, proposing new technologically advanced materials. This work aims to simulate these interesting glass-ceramics by using glass cullet coming from recycled municipal waste and high amount of iron(III) oxide (from 25 wt% to 50 wt%), the prevalent component of steel waste. The oxide was mixed with glass cullet and vitrified. The samples composition and the microstructure were investigated by scanning electron microscopy (SEM), and X-ray diffraction (XRD) was used to evaluate the nature of the crystalline phases. The chemical stability of the materials, in terms of ionic release into saline solution, was assessed. The electrical behavior of the samples was also investigated by varying the iron ions content and controlling the crystallization process. It is possible to obtain chemically stable materials with a nearly semiconducting behavior. Copyright (C) 2016, The editorial office of Journal of Materials Science & Technology. Published by Elsevier Limited.
引用
收藏
页码:1105 / 1110
页数:6
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