Effect of Stabilizer on Gold Leaching with Thiourea in Alkaline Solutions

The present work investigated the comparison of the effects of Na2SO3 and Na2SiO3 on thiourea stabilization, and a systematic study was undertaken to establish the effects of these stabilizers on the stability of alkaline thiourea, both qualitatively and quantitatively. The effects of these stabilizers on the activation energy of alkaline thiourea gold leaching was also studied. The results showed that sodium silicate was more suitable as a stabilizer in this system than sodium sulfite because the peak current of gold dissolution with sodium sulfite was higher than that with sodium silicate, but the inhibition of thiourea decomposition by the former was less obvious than that of sodium silicate in the cyclic voltammetry curve. The quartz crystal microbalance results showed that the quality decreased to about 100 ng cm2 in the presence of a stabilizer, while it increased to 300 ng cm2 in the absence of the stabilizer. It is inferred that gold can be dissolved by alkaline thiourea in the presence of a stabilizer, while it cannot without a stabilizer because of the decomposition of thiourea. This assumption was confirmed by atomic force microscopy measurements. The surface activation energy of Au dissolution decreased from 183.76 to 98.07 kJ/moL with the addition of sodium silicate, indicating that Au dissolution was promoted with the chemical.

Studies of the rate of gold sorption by the AM-2B anionite from cyanide-alkaline solutions

The paper presents the results of studies on the sorption leaching of gold-containing ore of the Vasilkovskoye deposit. Kinetic dependences of the sorption of gold and associated metals from cyanide-alkali solutions under different physical and chemical factors were obtained. It was found that gold on the AM-2B resin sorbed at a higher rate than, for example, copper and zinc. The solutions were analyzed using modern devices of a new generation: FT-IR spectrometer "Avatar 370". Laboratory studies were performed to determine the gold sorption rate by the AM-2B anionite from cyanide-alkaline solutions. It was found in the process of sorption of gold from multicomponent cyanide-alkali solutions on AM-2B anionite of mixed basicity, with the macroporous structure containing benzyl dimethylamine and dibenzyl dimethyl ammonium functional groups, that an important factor of qualitative and quantitative separation of gold and impurity metals is the concentration of cyanide and hydroxyl ions in solution. The temperature effect on the sorption rate of gold from cyanide-alkali solutions was studied with the temperature dependences F of t, Bt, of t, ln (l - F) of t, and D of t that show that the sorption process of dicyanoaurate ions is controlled by mixed diffusion.

Conversion of Carbohydrates in Lignocellulosic Biomass after Chemical Pretreatment

The aim of the study was to determine the quantitative and qualitative changes taking place in biomass components actively participating in methane fermentation, i.e., in carbohydrates, as a result of chemical pretreatment. Analyses were conducted on agricultural waste (corn stover, also called corn straw, and corncobs) as materials most commonly used in methane fermentation, as well as poplar wood, a material relatively rarely used in biogas production. Pretreatment with the aim of increasing efficiency of methane fermentation was carried out with the use of acid and alkaline solutions of different concentrations. The effect of pretreatment on carbohydrates was analyzed based on the quantitative and qualitative changes in this component. Due to the structural heterogeneity of carbohydrates, their varied reactivity and fermentability were determined in terms of holocellulose, cellulose, and pentosans. The chemical structure of cellulose was also analyzed. It is shown in this study that chemical pretreatment causes transformations of carbohydrate components, which differ quantitatively and qualitatively in the compared raw materials. It was found that the alkaline treatment caused smaller changes in the percentage shares of the carbohydrate biomass components as compared to the acid treatment. Moreover, it was observed that the compared materials differ in terms of quantitative changes in their chemical composition depending on the composition of the raw material prior to pretreatment. In the case of corn waste subjected to the action of 1 and 3% NaOH, the share of pentosans in the biomass increased. It was established that this is a change with a positive effect on fermentation efficiency. The action of acids and alkalis on the biomass led to similar structural changes in cellulose, which are adverse for the fermentation process.

Photolysis of the Insensitive Explosive 1,3,5-Triamino-2,4,6-trinitrobenzene (TATB)

The explosive 1,3,5-triamino-2,4,6-trinitrobenzene (TATB) is of particular interest due to its extreme insensitivity to impact, shock and heat, while providing a good detonation velocity. To determine its fate under environmental conditions, TATB powder was irradiated with simulated sunlight and, in water, under UV light at 254 nm. The hydrolysis of particles submerged in neutral and alkaline solutions was also examined. We found that, by changing experimental conditions (e.g., light source, and mass and physical state of TATB), the intermediates and final products were slightly different. Mono-benzofurazan was the major transformation product in both irradiation systems. Two minor transformation products, the aci-nitro form of TATB and 3,5-diamino-2,4,6-trinitrophenol, were detected under solar light, while 1,3,5-triamino-2-nitroso-4,6-dinitrobenzene, 1,3,5-triamino-2,4-dinitrobenzene and mono-benzofuroxan were produced under UV light. The product identified as 3,5-diamino-2,4,6-trinitrophenol was identical to the one formed in the dark under alkaline conditions (pH 13) and in water incubated at either 50 °C or aged at ambient conditions. Interestingly, when only a few milligrams of TATB were irradiated with simulated sunlight, the aci-isomer and mono-benzofurazan derivative were detected; however, the hydrolysis product 3,5-diamino-2,4,6-trinitrophenol formed only much later in the absence of light. This suggests that the water released from TATB to form mono-benzofurazan was trapped in the interstitial space between the TATB layers and slowly hydrolyzed the relatively stable aci-nitro intermediate to 3,5-diamino-2,4,6-trinitrophenol. This environmentally relevant discovery provides data on the fate of TATB in surface environments exposed to sunlight, which can transform the insoluble substrate into more soluble and corrosive derivatives, such as 3,5-diamino-2,4,6-trinitrophenol, and that some hydrolytic transformation can continue even without light.

Slippery Surface with Petal-like Structure for Protecting Al Alloy: Anti-corrosion, Anti-fouling and Anti-icing

The harsh working environment affects the performance and usage life of Al and its alloys, thus limiting their application. In recent years, Slippery Liquid-infused Porous Surface (SLIPS) has attracted much attention due to excellent anti-corrosion, anti-fouling and anti-icing properties. This may be an effective way to improve the properties of Al and its alloys. Here, the SLIPS with petal-like structure was constructed on the Al alloy via simple hydrothermal reaction, Stearic Acid (STA) modification and lubricant injection. A variety of droplets (including oil-in-water emulsions) can slide on the SLIPS at a low angle, even the Sliding Angle (SA) of the water droplet is only 3°. Furthermore, the SLIPS exhibits outstanding mechanical and chemical properties. It can maintain fine oil-locking ability under high shearing force and keep slippery stability after immersion in acid/alkaline solutions. In addition, the SLIPS possesses excellent anti-corrosion, anti-fouling and anti-icing properties, which provides a new way to promote the application of Al and its alloys. Therefore, the SLIPS is expected to be an effective way to improve the properties of Al and its alloys, as well as play a role in anti-fouling and self-cleaning in construction, shipbuilding and automotive manufacturing industries, thereby expanding the practical application of Al and its alloys.

Role of Mn addition on the general corrosion and pitting corrosion behavior of 13Cr stainless steel

Purpose The purpose of this study is to elucidate the effect of Mn addition on the corrosion behavior of stainless steel. Design/methodology/approach Chronoamperometry, quasi-steady-state polarization and electrochemical impedance spectroscopy were used to investigate the corrosion behavior of Mn added A13Cr-HS sample and original S13Cr samples. In addition, the corrosion product film was characterized by a field emission scanning electron microscope equipped with energy-dispersive spectroscopy and X-ray photoelectron spectroscopy. Findings The A13Cr-HS sample with 8 wt.% Mn addition maintained good general corrosion resistance in both acidic and alkaline solutions compared to the original S13Cr sample. Additionally, the A13Cr-HS sample had good pitting resistance in an alkaline solution containing Cl−, but a weaker resistance in an acidic solution. Originality/value The influence of Mn addition on the formation mechanism of the passive film was systematically analyzed.