An international comparative study of end-of-life vehicle (ELV) recycling systems

End-of-life vehicles (ELV) have become a global concern as automobiles have become popular worldwide. An international workshop was held to gather data and to discuss 3R policies and ELV recycling systems, their background and present situation, outcomes of related policies and programs, the framework of recycling and waste management, and case studies on related topics in several countries and regions, as well as the essential points of the comparison. Legislative ELV recycling systems are established in the EU, Japan, Korea, and China, while in the US, ELV recycling is managed under existing laws on environmental protection. Since automobile shredding residue (ASR) has a high calorific value and ash content, and includes heavy metals as well as a mass of unclassified fine particles, recycling ASR is considered highly difficult. Countries with a legislative ELV system commonly set a target for recovery rates, with many aiming for more than 95 % recovery. In order to reach this target, higher efficiency in ASR recovery is needed, in addition to material recycling of collectable components and metals. Environmentally friendly design was considered necessary at the planning and manufacturing stages, and the development of recycling systems and techniques in line with these changes are required for sound ELV management

バングラデシュにおける自然発生のヒ素汚染地下水に関する地球化学的研究 : 地下水中のヒ素濃度の空間分布を規制する要因について

広島大学(Hiroshima University)博士(理学)Physical Sciencedoctora

Enrichment mechanisms of antimony and arsenic in marine ferromanganese oxides: Insights from the structural similarity

Marine ferromanganese crusts and nodules as potential mineral deposits have received increasing attention. However, much less knowledge is available concerning the incorporation and enrichment mechanisms for antimony (Sb) and arsenic (As) in marine ferromanganese oxides. In this study, the surface complexations of Sb(V) and As(V) on synthetic ferrihydrite and Mn oxides (delta-MnO2 and birnessite) were investigated by a combination of adsorption experiments, extended X-ray absorption fine structure (EXAFS) analyses, and quantum chemical calculations. The speciation, distribution, and local structure of Sb and As in different types of natural marine ferromanganese oxides were determined by X-ray absorption near edge structure (XANES) and EXAFS analyses to reveal the enrichment mechanisms for the two elements in ferromanganese oxides at the molecular level. To the best of our knowledge, the Sb EXAFS analyses for different types of marine ferromanganese oxides are herein reported for the first time. Results showed that Sb(V) is preferentially adsorbed on Mn oxides through energetically favorable bidentate-mononuclear complexation because of the structural similarity between the octahedron Sb-v(OH)(6)(-) and MnO6 unit, although bidentate-binuclear (corner-sharing) and bidentate-mononuclear (edge-sharing) complexes can be formed on ferrihydrite and Mn oxides for the adsorption of Sb(V). By contrast, tetrahedral (AsO43-)-O-v - is mostly adsorbed on ferrihydrite and Mn oxides with the formation of bidentate-binuclear complexes. In natural marine ferromanganese oxides, Sb and As can be retained by Fe and Mn (oxyhydr)oxide components, and the disparate distribution of the two elements to Mn oxides may largely depend on the Mn/Fe ratio and constituent minerals. The larger enrichment factor of Sb than that of As in marine ferromanganese oxides may result from their preferential attachment modes onto the Fe and Mn phases and different inhibition effects from coexisting anions in seawater. Compared with As, a part of Sb may be strongly associated with the lateral sites in Mn oxides via the formation of bidentate edge-sharing complexes, with which anions such as sulfate in seawater do not significantly compete. The findings from this study provide the molecular-scale insights into the enrichment processes and mechanisms of Sb and As in marine ferromanganese oxides. Our study also helps elucidate the incorporation mechanisms and geochemical behaviors of other oxyanions in marine and surface environments. (C) 2019 Elsevier Ltd. All rights reserved