Enelton Fagnani

Sulfetos volatilizáveis por acidificação e metais extraídos simultaneamente na avaliação de sedimentos de água doce

This paper discusses the historical and methodological fundaments of the dynamics and quantification of acid volatile sulfides (AVS) and simultaneously extracted metals (SEM) in aquatic sediments. It also discusses the SEM/AVS relationship, which involves several controversial aspects such as sulfide stability, sulfide-organic matter interaction, and the inability to predict the toxicity of organic compounds in the environment. This relationship is an important tool for the inference of metal bioavailability. The use of ecotoxicological tests with target organisms regulated by international standards is also a relevant aspect.

Optimization of UV/H2O2 and ozone wastewater treatment by the experimental design methodology

ABSTRACT The objective of this study was to optimize UV/H2O2 and ozonation systems by means of an experimental design using as a response the efficiency of the operational conditions to remove the methylene blue (MB) dye. Two classes of experimental planning were used: the Doehlert matrix (DM) and the central composite design (CCD). The most important variables for each process were hydrogen peroxide concentration, the ratio of illuminated volume/total volume of the reactor and recirculation flow rate for UV/H2O2, and ozone flow rate, consumed ozone and MB concentration for the ozonation. The DM was more efficient in optimizing the systems, since it used a smaller number of experiments and achieved similar results when compared to the CCD. After optimization, the disinfection efficiency of the systems was tested with secondary effluent evaluating the inactivation of microbiological indicators, Escherichia coli and total coliforms, using the optimized and the worst condition previously obtained with MB removal as response. The inactivation efficiencies in the optimum conditions were about 99%, allowing an efficient disinfection as well as the production of an effluent with quality to be reused according to specific legislations, while at the worse conditions, the inactivation did not reach standards for reuse.

Response surface methodology applied to tropical freshwater treatment

ABSTRACT This paper presents the profits and disadvantages of the chemometrics approach instead of the one-factor-at-a-time (OFAT) coagulation diagram approach for tropical water physicochemical treatment. Central composite design associate to response surface methodology (CCD-RSM) is used to find the real best conditions for coagulant dosage and pH aiming at high-turbidity removal. The number of experiments needed to chemometrics model construction (12) is comparatively smaller than that used in the coagulation diagram (84), saving financial and environmental resources. Arguments for Water Treatment Plants (WTP) considering the replacement of coagulation diagram approach by the CCD-RSM approach in drinking water treatment are presented. Chemometrics models are all constructed on a free software platform, providing the best pH within the range 7.7–8.1, and the best coagulant dosage (polyaluminium chloride, PAC) between 2.0 and 3.1 mg Al2O3 L−1 (equivalent in mass). CCD-RSM provides a faster, lower-cost and more reliable alternative tool for WTP decision-making instead of the OFAT model, mainly for waters more affected by seasonal effects as can be seen in tropical and subtropical countries. GRAPHICAL ABSTRACT

The Dichromate Method versus the Photoelectrochemical Method: the Synergistic Influence of Turbidity and Chlorides on Chemical Oxygen Demand Analysis

This paper compares the dichromate method with the photoelectrochemical method (PeCOD), with regards to the influence of chloride and turbidity with chemical oxygen demand (COD) determination. Whereas the upper limits of chloride concentration are well established for both techniques, the influence of turbidity and the combined interference of underdosing chlorides and turbidity together have never been reported. When only potassium hydrogen phthalate or sorbitol were analyzed, the results show no significant difference in either method when 607 mg Cl L or 230 NTU of turbidity were added to the samples within the range of 100-900 mg L COD. However, a combined effect of these two interferents leads to significantly different results, mainly for low COD range, as evidenced by the Student’s t-test for paired samples (p = 0.05).

CONTROLE DA QUALIDADE NA DETERMINAÇÃO POTENCIOMÉTRICA DE SULFETOS VOLATILIZÁVEIS POR ACIDIFICAÇÃO (SVA) UTILIZANDO ADIÇÕES DE PADRÃO

This paper presents a quality assurance and quality control protocol in order to ensure the reliability of analytical results for the determination of acid volatile sulfides in environmental samples by potentiometry. The monitoring of the ion selective sensor readings must be realized continually and particularly in this situation where the analyte is susceptible to transformation and volatilization. Potentiometry with the standard addition was presented as a rapid, accurate, precise, feasible as well as a low cost technique. Concentrations of the analyte in the range of 0.49 to 1.02 mg L-1 were tested with percentage recoveries varying from 89 to 113%.

Determinação espectrofotométrica de hexametilenotetramina (HMT) em medicamentos, utilizando ácido cromotrópico e forno de micro-ondas

This paper proposes a methodology for spectrophotometric determination of hexamethylenetetramine (HMT) by using chromotropic acid in a phosphoric acid media employing a domestic microwave oven as a source of heating. The reddish-purple soluble product is quantitatively formed after 30 s of irradiation and obeys the Beer´s law in the range between 0.1-1.2 mg L-1 HMT (r = 0.99925). The method was applied successfully in commercial pharmaceutical preparations containing dyes in their composition. The results showed that the method proposed is feasible for simplicity, speed, low cost, precision and accuracy when compared with United States Pharmacopeia official method.