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- Development of a Turbidimetric Sequential Injection System to Monitor the Codfish Desalting ProcessPublication . Santos, Inês C.; Mesquita, Raquel B. R.; Galvis-Sánchez, Andrea C.; Delgadillo, Ivonne; Rangel, António Osmaro S. S.Salt-cured codfish represents an ancient process of preservation but requires the rehydration of the codfish with the correspondent salt removal. This work describes the development of a sequential injection system for the online turbidimetric determination of chloride during a simulated desalting process. The samples are directly aspirated to the manifold with no need for previous offline treatments; this was possible due to the use on an inline dialysis process; a quantification range from 50.0 mg/L to 20.0 g/L was established using the same manifold configuration. For monitoring the entire process, involving several chloride determinations (ca. 10), less than 3 mL of the desalting water was needed. Furthermore, the overall reagent consumption was quite low: 0.211 mg of AgNO3, 30.6 mg of HNO3, and 31.1 μg of PVA per determination. The accuracy of the system was evaluated by comparison with a potentiometric reference method. The determination rate was 28 and 31 h−1 according to the chloride concentration range. Several simulated desalting processes, under different conditions, were effectively monitored with the developed method.
- Iodine speciation in coastal and inland bathing waters and seaweeds extracts using a sequential injection standard addition flow-batch methodPublication . Santos, Inês C.; Mesquita, Raquel B. R.; Bordalo, Adriano A.; Rangel, António O. S. S.The present work describes the development of a sequential injection standard addition method for iodine speciation in bathing waters and seaweeds extracts without prior sample treatment. Iodine speciation was obtained by assessing the iodide and iodate content, the two inorganic forms of iodine in waters. For the determination of iodide, an iodide ion selective electrode (ISE) was used. The indirect determination of iodate was based on the spectrophotometric determination of nitrite (Griess reaction). For the iodate measurement, a mixing chamber was employed (flow batch approach) to explore the inherent efficient mixing, essential for the indirect determination of iodate. The application of the standard addition method enabled detection limits of 0.14 µM for iodide and 0.02 µM for iodate, together with the direct introduction of the target water samples, coastal and inland bathing waters. The results obtained were in agreement with those obtained by ICP-MS and a colorimetric reference procedure. Recovery tests also confirmed the accuracy of the developed method which was effectively applied to bathing waters and seaweed extracts.
- Potentiometric determination of fluoride with a flow system for the on-line monitoring of the fluorphenol degradation in a bioreactorPublication . Mesquita, Raquel B. R.; Santos, Inês C.; Pedrosa, Marta F. F.; Duque, Anouk F.; Castro, Paula M. L.; Rangel, António O. S. S.