Ammonium thiosulfate leaching is a promising alternative to the conventional cyanide method for extracting gold from ores. However, strategies for recovering gold from the leachate are less commercially used due to its low affinity to gold. The present study investigated the recovery of gold from the leachate using iron oxides (hematite, Fe2O3 or magnetite, Fe3O4). Cementation experiments were conducted by mixing 0.15 g of aluminum powder as an electron donor and 0.15 g of an electron mediator (activated carbon, hematite, or magnetite) in 10 mL of ammonium thiosulfate leachate containing 100 mg/L gold ions and 10 mM cupric ions for 24 h at 25 °C. The results of the solution analysis showed that when activated carbon (AC) was used, the gold was recovered together with copper (recoveries were 99.99% for gold and copper). However, selective gold recovery was observed when iron oxides were used, where the gold and copper recoveries were 89.7% and 21% for hematite and 85.9% and 15.4% for magnetite, respectively. An electrochemical experiment was also conducted to determine the galvanic interaction between the electron donor and electron mediator in a conventional electrochemical setup (hematite/magnetite–Al as the working electrode, Pt as the counter electrode, Ag/AgCl as the reference electrode) in a gold–thiosulfate medium. Cyclic voltammetry showed a gold reduction “shoulder-like” peak at −1.0 V using hematite/Al and magnetite/Al electrodes. Chronoamperometry was conducted and operated at a constant voltage (−1.0 V) determined during cyclic voltammetry and further analyzed using SEM-EDX. The results of the SEM-EDX analysis for the cementation products and electrochemical experiments confirmed that the gold was selectively deposited on the iron oxide surface as an electron mediator.

Multiple combinations of CeO2-Dolomite as fillers and Intumescent Flame Retardant (IFR) ingredients were used to optimize the intumescent coatings designed for I-beam steel substrates. The influenced of fillers and various combinations of flame-retardants on the fire protective performance of the coatings were evaluated using vertical Bunsen burner fire test and various characterization techniques. Formula C and Formula F having 1:1 and 2:2 CeO2-Dolomite ratio, obtained the lowest substrate temperature around 150oC and 150.4oC, respectively after 90 minutes fire exposure. Also, the morphological structures of intumescent char observed by SEM-EDX, demonstrated that Formula C and Formula F stimulated the formation of homogeneous and more compacted surface structure. X-ray photoelectron spectroscopy (XPS) provide the binding energies of C and O constituents, it was observed that [-(C2H4)n-] was the most important free radical as it could promote the formation of aromatic carbon chain in the char surface. Finally, the findings of this study revealed that the selection of appropriate fillers and combinations of flame-retardant ingredients significantly influenced the morphological structure of the char layer, of which, Formula C and Formula F produced a char with higher thermal stability, resulting to a more fire resistive IFR coating during fire exposure.

This study describes the effects of ceria (CeO 2) and dolomite [CaMg(CO 3) 2 ] additives on the pyrolysis behavior and fire resistive property of conventional intumescent flame retardant (IFR) coating system for I-beam steel substrate called ammonium polyphosphate-melamine-expandable graphite (APP-MEL-EG) system. The fire resistance of various formulations was evaluated using the standard vertical Bunsen burner fire test. Thermogravimetric analysis (TGA) was used to understand the degradation of coating formulations. Observations by scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX) demonstrated that significant amounts of additives favored the formation of homogeneous compacted char structures, which were predominantly composed of carbon (C), phosphorus (P) and oxygen (O). These three main components of the char were also found to be in various binding combinations with other lighter elements like nitrogen (N) and hydrogen (H) as illustrated by the attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy results. X-ray photoelectron spectroscopy (XPS) further suggest that polyethylene([(CH 2-C 2 H 2-CH 2) nÀ ]) free radicals were abundant on the char surface for the two best formulations and the binding energy of this radical promoted the formation of aromatic carbon chains that enhanced the char's thermal stability. This means that the selection of appropriate additives and combinations of flame-retardant ingredients could significantly change the morphology of the char layer and improve its thermal stability during fire exposure.

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