Selective leaching of rare earths, base metals and precious metals from used smartphones.

Discarded smartphones represent a valuable source of rare earths (REE), base metals and precious metals. This study focussed on the optimisation of three-stage selective leaching conditions for REE, copper and precious metals (Au and Ag), respectively, contained in printed circuit boards (PCBs) found in end-of-life smartphones. The effects of several leaching conditions, such as sulphuric acid and thiourea concentrations, were investigated using a statistical approach based on a design of experiments using Box-Behnken methodology.

Mass balance and economic study of a treatment chain for nickel, cobalt and rare earth elements recovery from Ni-MH batteries.

The aim of this project is to develop and evaluate the economic performance of a complete process for recovering nickel, cobalt, and rare earths (REEs) from nickel metal hydride (Ni-MH) battery waste. The main elements contained in the battery powder are Ni (523 g/kg), La (58 g/kg), Co (39 g/kg), Zn (21 g/kg), Nd (19 g/kg), Sm (19 g/kg) and Ce (14 g/kg). Metal leaching was carried out with 2 M sulfuric acid, solubilising 100% of Ni, 93% of Co and 94% of REEs.

Optimization of metals and rare earth elements leaching from spent Ni-MH batteries by response surface methodology.

The rechargeable battery market has almost doubled in 15 years. Regardless of the type of batteries, their limited lifespan means that sooner or later they will constitute a mass of waste whose management is problematic as their content is high in elements and metals of high economic interest, but also toxic to the environment. This project is to optimize the solubilization conditions for rare earth elements (REEs) and other metals from waste nickel-metal hydride (Ni-MH) batteries.

Nanobodies for the Early Detection of Ovarian Cancer.

Ovarian cancer ranks fifth in cancer-related deaths among women. Since ovarian cancer patients are often asymptomatic, most patients are diagnosed only at an advanced stage of disease. This results in a 5-year survival rate below 50%, which is in strong contrast to a survival rate as high as 94% if detected and treated at an early stage.

Disaster risk management system in Vietnam: progress and challenges.

Background: Vietnam is one of the countries most impacted by disasters in Asia- Pacific. Floods, droughts and storms are the most common catastrophes. These risks endanger millions of lives and create massive financial and production losses.

Optimized indium solubilization from LCD panels using HSO leaching.

Spent liquid crystal displays (LCDs) are a secondary source of precious/strategic metals, including indium (In). The present study involved optimizing the solubilization of this strategic element from samples of indium tin oxide (ITO) glass prepared from LCD screens of computer monitors and laptop screens. The influence of operating conditions on In solubilization, as well as optimum conditions for sulfuric acid leaching were defined by a Box-Behnken-type experimental design methodology.

Roles of Active-Site Aromatic Residues in Cold Adaptation of Esterase EstSP1.

The aromatic amino acids, Tyr or Trp, which line the active-site walls of esterases, stabilize the catalytic His loop via hydrogen bonding. A Tyr residue is preferred in extremophilic esterases (psychrophilic or hyperthermophilic esterases), whereas a Trp residue is preferred in moderate-temperature esterases. Here, we provide evidence that Tyr and Trp play distinct roles in cold adaptation of the psychrophilic esterase EstSP1 isolated from an Arctic bacterium PAMC 26605.

Optimizing removal of arsenic, chromium, copper, pentachlorophenol and polychlorodibenzo-dioxins/furans from the 1-4 mm fraction of polluted soil using an attrition process.

The objective of this study was to evaluate, at a pilot scale, the performance of an attrition process for removing As, Cr, Cu, pentachlorophenol (PCP) and polychlorodibenzodioxins and furans (PCDDF) from a 1-4 mm soil fraction. A Box-Behnken experimental design was utilized to evaluate the influence of several parameters (temperature, surfactant concentration and pulp density) and to optimize the main operating parameters of this attrition process. According to the results, the concentration of surfactant (cocamidopropylbetaine-BW) was the main parameter influencing both PCP and PCDDF removal from the 1-4 mm soil fraction by attrition.

Degradation of polycyclic aromatic hydrocarbons in different synthetic solutions by Fenton's oxidation.

The Fenton oxidation using phenanthrene (Phe), fluoranthene (Fle) and benzo[a]pyrene (BaP) as representative polycyclic aromatic hydrocarbon (PAH) contaminants was examined. The effect of the HO concentration, the temperature and the competition between the PAHs in different solutions (methanol, surfactant and quartz) was investigated. The Fenton oxidation process was performed at pH = 2.

Coupling extraction-flotation with surfactant and electrochemical degradation for the treatment of PAH contaminated hazardous wastes.

The performance of a two-stage process combining extraction of polycyclic aromatic hydrocarbons (PAHs) with an amphoteric surfactant (CAS) followed by electro-oxidation of PAH-foam concentrate was studied for the decontamination of aluminum industry wastes (AIW) and polluted soils. The PAH suspensions extracted from AIW and soils were treated in a 2L-parallelepipedic electrolytic cell containing Ti/RuO2 anodes and stainless steel cathodes. Current densities varying from 4.

Electrochemical degradation of polycyclic aromatic hydrocarbons in creosote solution using ruthenium oxide on titanium expanded mesh anode.

In this study, expanded titanium (Ti) covered with ruthenium oxide (RuO(2)) electrode was used to anodically oxidize polycyclic aromatic hydrocarbons (PAH) in creosote solution. Synthetic creosote-oily solution (COS) was prepared with distilled water and a commercial creosote solution in the presence of an amphoteric surfactant; Cocamidopropylhydroxysultaine (CAS). Electrolysis was carried out using a parallelepipedic electrolytic 1.