thiourea and sulfuric-acid

Present study is a critical analysis and subsequent development of an analytical tool to measure the total sugar concentration in a carbohydrate mixture comprising both hexose and pentose. For this purpose, individual sugars were measured and standardized with anthrone reagent prepared in an ice-cold 98 % sulphuric acid followed by 3 min of boiling. Furthermore, regression analysis was performed after mathematical manipulation with the individual standards to formulate a linear relation between the absorbance of the mixture and its concentration, which satisfies Beer's law. It was found that the correlation coefficient for the equation is 0.973, when confidence interval was set at 0.95. The validation was done with a synthetic mixture of concentrations at 0.17 and 0.22 g/L (as range was ensured between 0.1 and 0.3 g/L) and also with the carbohydrate mixture as the prehydrolyzate obtained after the pretreatment of banana stem, which showed around 94.1 % accuracy and higher sensitivity with the cellulose present in the mixture. Thus, the method is evident to quantify the total sugars accurately obtained from hydrolyzed lignocellulosic biomass.

Topics: Anthracenes; Carbohydrates; Regression Analysis; Spectrophotometry; Sulfuric Acids; Thiourea

In this work, a flow injection analysis (FIA) method was introduced for the determination of trace amounts of thiourea in tap water. This method is based upon the inhibition effect of thiourea on the reaction between meta-cresol purple (MCP) and potassium bromate catalyzed by bromide ions in a sulfuric acid medium. In the presence of thiourea, an induction period appears in the reaction system, and as a result, the absorbance of MCP increases at 525 nm in the FIA manifold. The chemical and FIA variables are studied and optimized using the univariate and Simplex optimization methods. Under the optimum conditions, thiourea can be determined in the range of 0.100-13.0 μg mL(-1). The limit of detection (3σ) for thiourea was found to be 0.0310 μg mL(-1). The relative standard deviations (RSDs) for six replicate determinations of 0.500, 5.00, and 12.0 μg mL(-1) of thiourea were 4.0%, 1.8%, and 1.2%, respectively. The proposed method was also applied for the determination of thiourea in orange juice and orange peel samples with recoveries in the range of 98.0-101%. The analytical speed of the method was calculated to be about 120 sample per hour.

Topics: Beverages; Bromates; Bromides; Citrus sinensis; Flow Injection Analysis; Indicators and Reagents; Online Systems; Osmolar Concentration; Potassium Compounds; Rheology; Spectrophotometry; Sulfuric Acids; Temperature; Thiourea; Water

A novel hydrometallurgical process was proposed for selective recovery of Cu, Ag, Au and Pd from waste printed circuit boards (PCBs). More than 99% of copper content was dissolved by using two consecutive sulfuric acid leaching steps in the presence of H2O2 as oxidizing agents. The solid residue of 2nd leaching step was treated by acidic thiourea in the presence of ferric iron as oxidizing agent and 85.76% Au and 71.36% Ag dissolution was achieved. The precipitation of Au and Ag from acidic thiourea leachate was investigated by using different amounts of sodium borohydride (SBH) as a reducing agent. The leaching of Pd and remained gold from the solid reside of 3rd leaching step was performed in NaClO-HCl-H2O2 leaching system and the effect of different parameters was investigated. The leaching of Pd and specially Au increased by increasing the NaClO concentration up to 10V% and any further increasing the NaClO concentration has a negligible effect. The leaching of Pd and Au increased by increasing the HCl concentration from 2.5 to 5M. The leaching of Pd and Au were endothermic and raising the temperature had a positive effect on leaching efficiency. The kinetics of Pd leaching was quite fast and after 30min complete leaching of Pd was achieved, while the leaching of Au need a longer contact time. The best conditions for leaching of Pd and Au in NaClO-HCl-H2O2 leaching system were determined to be 5M HCl, 1V% H2O2, 10V% NaClO at 336K for 3h with a solid/liquid ratio of 1/10. 100% of Pd and Au of what was in the chloride leachate were precipitated by using 2g/L SBH. Finally, a process flow sheet for the recovery of Cu, Ag, Au and Pd from PCB was proposed.

Topics: Algorithms; Borohydrides; Chemical Precipitation; Copper; Electronic Waste; Gold; Hydrochloric Acid; Hydrogen Peroxide; Palladium; Sodium Hypochlorite; Sulfuric Acids; Thiourea

The present lab-scale experimental study presents the process of leaching waste printed circuit boards (WPCBs) in order to recover gold by thioureation. Preliminary tests have shown that copper adversely affects gold extraction; therefore an oxidative leaching pre-treatment was performed in order to remove base metals. The effects of sulfuric acid concentration, hydrogen peroxide volume and temperature on the metal extraction yield were studied by analysis of variance (ANOVA). The highest copper extraction yields were 76.12% for sample A and 18.29% for sample D, after leaching with 2M H2SO4, 20 ml of 30% H2O2 at 30°C for 3h. In order to improve Cu removal, a second leaching was performed only on sample A, resulting in a Cu extraction yield of 90%. Other experiments have shown the negative effect of the stirring rate on copper dissolution. The conditions used for the process of gold extraction by thiourea were: 20 g/L thiourea, 6g/L ferric ion, 10 g/L sulfuric acid, 600 rpm stirring rate. To study the influence of temperature and particle size, this process was tested on pins manually removed from computer central processing units (CPUs) and on waste CPU for 3½ h. A gold extraction yield of 69% was obtained after 75% of Cu was removed by a double oxidative leaching treatment of WPCBs with particle sizes smaller than 2 mm.

Topics: Analysis of Variance; Copper; Electronic Waste; Gold; Hydrogen Peroxide; Recycling; Sulfuric Acids; Temperature; Thiourea

A new, selective and sensitive on-site spectrophotometric method for the determination of antimony at trace level in water, soil and dust samples of Central India has been demonstrated. It is based on the color reaction of Sb(III) with I(-) ions in the presence of a cationic surfactant cetylpyridinium chloride (CPC) in acidic media, and subsequent extraction of the complex with N-phenylbenzimidoylthiourea (PBITU) into chloroform to give a yellow colored complex. The value of apparent molar absorptivity of the complex in the terms of Sb is (7.84) x 10(4)l mol(-1)cm(-1) at 440 nm. The detection limit of the method is 5 ng ml(-1). In addition, the present method is free from interferences of all metal ions that are associated during the determination of antimony in environmental samples.

Topics: Antimony; Chloroform; Dust; Environmental Monitoring; Environmental Pollutants; Hydrochloric Acid; India; Potassium Iodide; Rain; Rivers; Soil; Spectrophotometry, Ultraviolet; Sulfuric Acids; Surface-Active Agents; Thiourea; Waste Disposal, Fluid

Quaternary ammonium salt has strong affinity with gold in cyanide solutions, but it is not readily stripped. Stripping with acidic thiourea solutions and air sparging shows promise. There are some reports on the process of thiourea stripping, but little about its mechanism. In this paper, the stripping mechanism of N263/sulphuric thiourea/alkaline cyanide gold solution is studied by EXAFS. According to the experiments, sulphuric acid, thiourea and gold-thiourea complex can be extracted by N263 as a neutral molecule, and the stripping process can be described as following: (1) Sulphuric acid and thiourea are extracted by N263; (2) In organic phase, gold-cyanide complex is converted to gold-thiourea complex, which exists as Au[SC(NH2)2]2HSO4, and CN- forms HCN with acid at the same time; (3) HCN is removed by air sparging, and Au[SC(NH2)2]2HSO4 is distributed between organic phase and liquor phase, most of which transfers to liquor phase and is stripped.

Topics: Amines; Cyanates; Cyanides; Electrochemistry; Environmental Monitoring; Gold; Hydrogen-Ion Concentration; Metal Nanoparticles; Nanotechnology; Pharmaceutical Solutions; Quaternary Ammonium Compounds; Reagent Strips; Solutions; Sulfuric Acids; Thiourea

The concentrations of gold in thiourea and sulfuric acid solutions using gold standard solutions in diluent royal water were determined by AAS. The linear range was 0.2-12 x 10(-6), and RSD < 5%. This method simplifies the analysis of gold in thiourea and sulfuric acid solution. Thiourea declines the absorbency of gold while sulfuric acid plays a contrary role. The determined value were satisfactor after being modified by the blank curve.

Topics: Gold; Reproducibility of Results; Solutions; Spectrophotometry, Atomic; Sulfuric Acids; Thiourea

In previous studies we have shown interactions between ozone and acidic respirable aerosols as evaluated by sensitive biochemical and quantitative morphological endpoints. In the present paper we have attempted to test the hypothesis that active oxygen species might play a role in lung damage caused by ozone +/- sulfuric acid aerosol. Rats were administered various scavengers of active oxygen species via the intraperitoneal (i.p.) route before and during exposure to 0.12, 0.20, or 0.64 ppm of ozone +/- 0.04, 0.1, 0.2, 0.5, or 1.0 mg/m3 of sulfuric acid aerosol. Vitamin E, a lipid-soluble free radical scavenger, beta-carotene (the precursor of vitamin A), a singlet oxygen scavenger, and dimethylthiourea, a hydrogen peroxide scavenger, were tested. Dimethylthiourea at doses of 50-500 mg/kg per day was able to protect rats from the effects of ozone, suggesting a role for hydrogen peroxide in ozone-induced lung damage in vivo. Neither vitamin E nor beta-carotene at 100 mg/kg doses had any protective activity in our experiments, despite documentation of increased lung content of the scavengers in animals receiving these agents. These results suggest that water solubility may play a role in the efficacy of the scavenging agents under our exposure protocols. We conclude that: (1) hydrogen peroxide may be involved in ozone-induced lung damage; and (2) that lung injury by ozone and by ozone + sulfuric acid aerosol may share common pathways.

Topics: Aerosols; Animals; beta Carotene; Carotenoids; Collagen; Drug Synergism; Free Radicals; Lung; Male; Oxygen; Ozone; Proteins; Rats; Rats, Inbred Strains; Sulfuric Acids; Thiourea; Vitamin E