New accurate, precise, and sensitive spectrophotometric method were developed for the assay of L-ascorbic acid in pharmaceutical preparations. The determination of L-ascorbic acid was based on its oxidation by potassium peroxydisulfate in the presence of Ag(I) as a catalyst. The molar absorptivity of the proposed method was found to be 8.61 · 103 L mol-1 cm-1 at 248 nm. Beer's law was obeyed in the concentration range of 0.46–20.0 μg mL–1. Other compounds commonly found in vitamin C and multivitamin products did not interfere with the determination of L-ascorbic acid. The proposed method was successfully applied for the determination of L-ascorbic acid in pharmaceutical formulations. The results obtained with the proposed method showed good agreement with those given by the titrimetric method using iodine.

In addition to soda, the Solway production process yields large amounts of waste sludge that contains a high percentage of CaCO3 and Ca(OH)2. In this paper, solid waste sludge from a soda factory in Bosnia and Herzegovina of a certain granulation was used to remove metal ions from the binary system initial concentrations of 500 mg/L. The research results showed that the precipitation efficiency for the binary system Cu - Ni was 99.810% at a pH of 11.42 for Cu2+ and 99.896% for Ni2+ at a pH of 10.86, while for the binary system Pb - Zn it was 99.84% at the same pH value of 10.64. This research has shown that it is very difficult to separate and remove metal precipitation from binary systems because the optimal pH for one metal does not correspond to another metal.

Two new, accurate, precise, and sensitive spectrophotometric methods were developed for the assay of L-ascorbic acid in pharmaceutical preparations. The determination of L-ascorbic acid was based on its oxidation by potassium peroxymonosulfate (method A) and hydrogen peroxide in the presence of Cu(II) as a catalyst (method B). The molar absorptivities were found to be 1.48×10 and 1.06×10 L mol cm for methods A and B, respectively. Beer's law was obeyed in the concentration range of 0.65–11.20 μg mL for method A and 0.51–16.00 μg mL for method B. Other compounds commonly found in vitamin C and multivitamin products did not interfere with the determination of L-ascorbic acid.. The proposed methods were successfully applied for the determination of L-ascorbic acid in pharmaceutical formulations. The results obtained with the proposed methods showed good agreement with those given by the titrimetric method using iodine.