The use of L-ascorbic acid in speciation of arsenic compounds in drinking water

Arsenic speciation, besides total arsenic content determination, is very important in analysis of water, foodstuffs, and environmental samples, because of varying degrees of toxicity of different species. For such purpose hydride generation atomic absorption spectrometry can be used based on the generation of certain types of hydride, depending on the pH value and pretreatment in different reaction media. In this study, we have investigated the effect of L-ascorbic acid as the reaction medium as well as the pre-reducing agent in speciation of arsenic by hydride generation-atomic absorption spectrometry in order to determine monomethyl arsonic acid (MMA) in the presence of inorganic forms of arsenic

Determination of As(III) and As(V) in waters by chronopotentiometric stripping analysis

Arsenic is a naturally occurring toxic and carcinogenic element. The degree of the toxicity depends on its chemical form and the concentration. Application of a sensitive, selective, simple and rapid method for detection and monitoring of different oxidation states of arsenic in waters is of great importance because main route of population exposure is through drinking water. In this work chronopotentiometric stripping analysis (CSA) was used for the determination of As(III) and As(V) in tap, well, river and rain waters from Vojvodina (Serbia). Gold film electrode on the glassy carbon support was used as the working electrode. The experimental parameters of the technique were investigated and optimized. Detection limit of the method for the electrolysis time of 600 s was 2 μg/dm3 of As(III)

Chronopotentiometric stripping analysis of selenium using mercury film electrode

The influence of the most important experimental factors in chronopotentiometric stripping analysis (CSA) of selenium( IV) using mercury film working electrode was examined. Interferences of copper, iron and lead were investigated as well. The possibility of avoiding prolonged deaeration of the solution was examined by applying medium exchange modification of the technique, where the dissolution of the deposit was performed in calcium-chloride solution. Detection limits obtained for the modification of the CSA with prior deaeration and medium exchange modification were 0.4 μg/dmJ and 1.15μg/dmJ, respectively. Accuracy of the defined techniques has been confirmed by analysing reference material (RM 8436) -wheat durum flour. The results obtained by applying both modifications of the technique showed a very good agreement of total selenium content with declareted value

Determination of sensitivity limit in quantative analysis of polycyclic aromatic hydrocarbons by Gc-ms

The limit of detection (LOD) and the limit of quantitation (LOQ) for 16 individual PAHs from the Environmental Protection Agency (EPA) list (naphthalene, acenaphthylene, acenaphtene, fluorene, phenanthrene antrachene, fluoranthene, pyrene, benzo(a)anthracene, chrysene benzo(b)fluoranthene, benzo(k)fluoranthene, benzo(a)pyrene, dibenzo(a,h) anthracene, benzo(g,h,i)perylene and indeno(1,2,3-cd)pyrene) were determined by Gas Chromatography – Mass Spectrometry (GC-MS). Determination was performed by SCAN (digital linear scanning) and SIM (selected ion monitoring) techniques preceded by the optimization of the experimental factors. The limit of detection obtained by the SCAN technique was in the range of 0.179 – 15.236 ng, and the quantitation limit in the range of 1.017 – 50.788 ng. SIM technique enabled LOD and LOQ in the range of 0.036 – 13.886 pg and 0.119 – 46.287 pg respectively

Determination of polycyclic aromatic hydrocarbons in soil by gas chromatography-mass spectrometry

Polycyclic aromatic hydrocarbons (PAHs) were determined in soil samples from forty different locations in Vojvodina. The samples were Soxhlet extracted cleaned-up and analyzed using gas chromatography-mass spectrometry (GC-MS) in the selected ion monitoring mode (SIM). Each PAH was separately quantified using an eight-point calibration of mixed standard solutions in the range between 0.25 and 10 μg/cm3. The sum of the 16 US Environmental Protection Agency PAHs analyzed in the soil samples varied from 0.043 to 1.362 mg/kg of dry soil

Determina tion of diacetyl and 2,3-pentanedione in beer by gc/ms using solid-phase extraction columns

A new GC/MS method for the determination of diacetyl and 2,3-pentanedione was investigated. Diacetyl and 2,3-pentanedione were derivatized with 1,2-diaminobenzene to form 2,3-dimetylquinoxaline and 2-ethyl-3-methylquinoxaline. respectively. The amounts of formed 2.3-dimetylqu:inoxaline and 2-ethyl-3,.methylquinoxaline were proportional to the concentrations of diacetyl and 2,3-penianedione present in the sample. 2,3-Dimetylquinoxaline and 2-ethyl-3-methylquinoxaline were extracted by solid-phase extraction (SPE) columns and determined by gas chromatography using a mass selective detector. This method was applied for the determination of diacetyl and 2,3-pentanedione concentrations in beer. Extraction by SPE columns proved to be very simple and reliable. The method can be used for simultaneous determination of diacetyl and 2,3-pentanedione concentrations in beer in a great number of beer samples