铁矿企业发展循环经济的模式选择

论述了我国铁矿企业加快发展循环经济的重要性和紧迫性,通过对国家循环经济试点单位的调研,提出铁矿企业发展循环经济可以采取“两提高、三综合、一恢复”的模式,即提高采矿回采率和出矿品位,提高选矿金属回收率和精矿品位;矿产资源综合利用;恢复矿山生态环境。并就铁矿企业如何大力发展循环经济提出建议。     

包钢三合明铁矿开发对生态环境的影响

《包钢三合明铁矿区西部异常区矿产资源开发利用工程》是以地下采矿和湿法磁选选矿为生产工艺流程的建设项目,本文根据工程项目的特性、建设内容、生态影响识别,结合工程厂址周围环境特征,重点分析了工程建设期、运营期对周围生态环境的影响,并提出相应防治对策。     

Characterization and acid-mobilization study for typical iron-bearing clay mineral

In this study, iron speciation in five standard clay samples was characterized. Iron mobilization from these clays was then measured in acidic media. For comparison, a commercially available Arizona test dust (ATD) was also observed. The results showed that the free-Fe contents of clays were commonly lower than that of dust aerosols. The components of clays were dominant by the structural Fe held in the aluminosilicate lattice. The iron solubility of the clays were in the order of KGa-2?>?SWy-2?>?CCa-2?>?IMt-2?>?NAu-2. Based upon the Mössbauer spectrum and transmission electron microscopy (TEM) analysis, the Fe(II) fraction and the Fe/Si ratio of clay particles changed after dissolution, suggesting the total Fe solubility depended on the Fe atom states existing within the aluminosilicate lattice. The Fe in KGa-2 and SWy-2 was most likely substituted for alkaline elements as the interlayer ions held by ionic bonds in the aluminosilicate, which are more liable to dissolution. However, the Fe in NAu-2 was more likely to be bound by strong covalent bonds in aluminosilicate mineral, which is less soluble. The much highly soluble Fe in ATD was not only linked to the dissolution of an appreciable fraction of Fe(II), but also could be attributed to the fact that the Fe bonds in the clay fraction of ATD were mainly present as ionic bonds. The TEM images showed that reacted clay particles displayed less aggregate particles, with nanoparticle aggregates and the Fe/S-rich tiny particles attached to the remains.     

西湖水体中铁铝钙镁的环境行为探讨

研究西湖水中铁，铝，钙，镁的含量分布，水平方向的动态交换，以及在引物水期与非引水期的变化，探讨这些元素在西湖水体自净中的作用。     

无机高分子混凝剂的发展与应用

讨论了不同类型无机高分子混凝剂的混凝机理、生产及应用，并指出了新型混凝剂的研制方向．     

Refining mercury emission estimations to the atmosphere from iron and steel production

正Due to its long-range transport in the atmosphere,mercury is a pollutant of global concern with health risks to humans and ecosystems worldwide(Li et al.,2012;Lindqvist et al.,1991;Liu et al.,2012a;Tang et al.,2016;Wang et al.,2015;Shao et al.,2016).Atmospheric mercury,mainly from emission from various natural and anthropogenic sources and     

Hidden values in bauxite residue (red mud): Recovery of metals

Bauxite residue (red mud) is a hazardous waste generated from alumina refining industries. Unless managed properly, red mud poses significant risks to the local environment due to its extreme alkalinity and its potential impacts on surface and ground water quality. The ever-increasing generation of red mud poses significant challenges to the aluminium industries from management perspectives given the low proportion that are currently being utilized beneficially. Red mud, in most cases, contains elevated concentrations of iron in addition to aluminium, titanium, sodium and valuable rare earth elements. Given the scarcity of iron supply globally, the iron content of red mud has attracted increasing research interest. This paper presents a critical overview of the current techniques employed for iron recovery from red mud. Information on the recovery of other valuable metals is also reviewed to provide an insight into the full potential usage of red mud as an economic resource rather than a waste. Traditional hydrometallurgy and pyrometallurgy are being investigated continuously. However, in this review several new techniques are introduced that consider the process of iron recovery from red mud. An integrated process which can achieve multiple additional values from red mud is much preferred over the single process methods. The information provided here should help to improve the future management and utilization of red mud.     

Effect of iron ion configurations on Ni2+ removal in electrocoagulation

Electrocoagulation (EC) has been widely used to treat the heavy metal wastewater in industry. A novel process of sinusoidal alternating current electrocoagulation (SACC) is adopted to remove Ni²⁺ in wastewater in this study. The morphology of precipitates and the distribution of the main functional iron configurations were investigated. Ferron timed complex spectroscopy can identify the monomeric iron configurations [Fe(a)], oligomeric iron configurations [Fe(b)] and polymeric iron configurations [Fe(c)]. The optimal operating conditions of SACC process were determined through single-factor experiments. The maximum Ni²⁺ removal efficiency [Re(Ni²⁺)] was achieved under the conditions of pH₀=7, current density (j) = 7 A/m², electrolysis time (t) = 25 min, c₀(Ni²⁺) = 100 mg/L. At pH=7, the proportion of Fe(b) and Fe(c) in the system was 50.4 at.% and 23.1 at.%, respectively. In the SACC process, Fe(b) and Fe(c) are the main iron configurations in solution, while Fe(c) are the vast majority of the iron configurations in the direct current electrocoagulation (DCC) process. Re(Ni²⁺) is 99.56% for SACC and 98.75% for DCC under the same optimum conditions, respectively. The precipitates produced by SACC have a high proportion of Fe(b) configurations with spherical α-FeOOH and γ-FeOOH structures which contain abundant hydroxyl groups. Moreover, it is demonstrated that Fe(b) has better adsorption capacity than Fe(c) through adsorption experiments of methyl orange (MO) dye. Fe(a) configurations in the homogeneous solution had no effect on the removal of nickel.     

Rapid and long-effective removal of broad-spectrum pollutants from aqueous system by ZVI/oxidants

• The coupling of oxidants with ZVI overcome the impedance of ZVI passive layer. • ZVI/oxidants system achieved fast and long-effective removal of contaminants. • Multiple mechanisms are involved in contaminants removal by ZVI/oxidant system. • ZVI/Oxidants did not change the reducing property of ORP in the fixed-bed system. Zero-valent iron (ZVI) technology has recently gained significant interest in the efficient sequestration of a wide variety of contaminants. However, surface passivation of ZVI because of its intrinsic passive layer would lead to the inferior reactivity of ZVI and its lower efficacy in contaminant removal. Therefore, to activate the ZVI surface cheaply, continuously, and efficiently is an important challenge that ZVI technology must overcome before its wide-scale application. To date, several physical and chemical approaches have been extensively applied to increase the reactivity of the ZVI surface toward the elimination of broad-spectrum pollutants. Nevertheless, these techniques have several limitations such as low efficacy, narrow working pH, eco-toxicity, and high installation cost. The objective of this mini-review paper is to identify the critical role of oxygen in determining the reactivity of ZVI toward contaminant removal. Subsequently, the effect of three typical oxidants (H₂O₂, KMnO₄, and NaClO) on broad-spectrum contaminants removal by ZVI has been documented and discussed. The reaction mechanism and sequestration efficacies of the ZVI/oxidant system were evaluated and reviewed. The technical basis of the ZVI/oxidant approach is based on the half-reaction of the cathodic reduction of the oxidants. The oxidants commonly used in the water treatment industry, i.e., NaClO, O₃, and H₂O₂, can be served as an ideal coupling electron receptor. With the combination of these oxidants, the surface corrosion of ZVI can be continuously driven. The ZVI/oxidants technology has been compared with other conventional technologies and conclusions have been drawn.     

Phytoavailability and Fractions of Iron and Manganese in Calcareous Soil Amended with Composted Urban Wastes

Little is known about the effects of applying composted urban wastes on the phytoavailability and distribution of iron (Fe) and manganese (Mn) among chemical fractions in soil. In order to study this concern several experiments in pots containing calcareous soil were carried out. The received treatments by adding separately two rates (20 and 80 Mg ha^?1) of municipal solid waste (MSW) compost and/or municipal solid waste and sewage sludge (MSW-SS) co-compost. The cropping sequence was a lettuce crop followed by a barley crop. It was observed that treatments amended with composted urban wastes tended to promote slight increases in lettuce yield compared to the control. The highest Fe levels in lettuce were found when higher rates of MSW-SS co-compost were applied; these values were significant compared to those obtained in the other treatments. In all cases, the application of organic materials increased the concentration and uptake of Mn in lettuce compared to the control; however, these increases were significant only when higher rates of MSW compost were applied. The organic amendments had beneficial delayed effects on barley yields, showing, in most cases, significant increases compared to the control. In this context, treatments with MSW compost were found to be more effective than the equivalent treatments amended with MSW-SS co-compost. Compared to the control, composted urban wastes increased Fe concentration in straw and rachis, and decreased Fe concentration in barley grain. Similarly, a decreased concentration of Mn in the dry matter of barley crop grown in soils treated with composted urban wastes was observed.