A simple spectrophotometric method is developed for the determination of phosphate in sugar cane juice, water and detergent samples. The method is based on the formation of phosphomolybdate with added molybdate followed by its reduction with sodium sulphide in aqueous sulfuric acid medium. The system obeys Lambert-Beer’s law at 715 nm in the concentration range 0.3-12.24 ppm. Molar absorptivity, correlation coefficient and Sandell’s sensitivity values were found to be 6.1x103mol-1cm-1, 0.999 and 0.0156 µg cm-2respectively. The results obtained were reproducible with acceptable standard deviation 3.7% and relative error 3.4%. For a comparison of the method phosphate present in various samples were also determined separately following an official method. The results of the developed method compare well with those of the official method.

1 volumetric [6, 19] as well as other methods [12-16] when sulfur dioxide is in low concentrations, because of its simplicity and cost-effective instrumentation. However, one of the spectrophotometric methods [20] employs rosaniline and formaldehyde, which are considered to be toxic [21]. Another AOAC method [22] requires the use of the dye thymol blue, a known pH indicator. Obviously, the method requires the strict control of pH and also suffers from a narrow range of sulfur dioxide determination. Therefore, a new spectrophotometric method for sulfur dioxide is developed in our work. The method is based on the formation of a redbrown peroxovanadate complex [23-25], λ max = 470 nm, from ammonium metavandate and hydrogen peroxide in 2 M sulfuric acid. When sodium metabisulfite (Na 2 S 2 O 5 = 2SO 2) is added, it preferentially reacts with hydrogen peroxide, thereby decolorizing the peroxovanadate complex until its concentration is less than that of the complex.

A novel, simple, sensitive spectrophotometric method is proposed for the determination of five phenothiazines. Chloramine-T with iodine in acetic acid produces iodine monochloride which oxidizes phenothiazines to absorbing cations. Those would associate later with unreacted ICl to form an ion pair, [Ph+] [ICl-(2)] in hydrochloric acid medium. These appear to provide exceptional color stability to the systems. A probable mechanism along with experimental stoichiometry and stability constants of such ion pairs is indicated. The method is not only successful in stabilizing the color of the systems, but also in making a unique observation of two regions of concentration of phenothiazines adhering separately to Beer's law. The results obtained from the analyses of pure samples and their drug formulations in both regions of concentration are comparable with those obtained either with a reported titrimetric method or with a British Pharmacopoeia (B.P.) UV-spectrophotometric method. The conditions required for the quantitative determination of phenothiazines are described and related analytical parameters are also calculated.

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The proposed work describes a simple spectrophotmetric as well as a titrimetric method to determine sulfur dioxide. The spectrophotometric method is based on a redox reaction between sulfur dioxide and iodine monochloride obtained from iodine with chloramine-T in acetic acid. The reagent iodine monochloride oxidizes sulfur dioxide to sulfate, thereby reducing itself to iodine. Thus liberated iodine will also oxidize sulfur dioxide and reduce itself to iodide. The obtained iodide is expected to combine with iodine to form a brown-colored homoatomictriiodide anion (460 nm), which forms an ion-pair with the sulfonamide cation, providing exceptional color stability to the system under an acidic condition, and is quantitatively relatd to sulfur dioxide. The system obeys Beer's law in the range 5 - 100 microg of sulfur dioxide in a final volume of 10 ml. The molar absorptivity is 5.03 x 10(3) l mol(-1)cm(-1), with a relative standard deviation of 3.2% for 50 microg of sulfur dioxide (n = 10). In the titrimetric method, the reagent iodine monochloride was reduced with potassium iodide (10%) to iodine, which oxidized sulfur dioxide to sulfate, and excess iodine was determined with a thiosulfate solution. The volume difference of thiosulfate with the reagent and with the sulfur dioxide determined the sulfur dioxide. Reproducible and accurate results were obtained in the range of 0.1 - 1.5 mg of sulfur dioxide with a relative standard deviation of 1.2% for 0.8 mg of sulfur dioxide (n = 10).