Urban river recovery: a systematic review on the effectiveness of water clean-up programs.

Urban rivers are affected at different levels by the intensification of human activities, representing a serious threat to the maintenance of terrestrial life and sustainable urban development. Consequently, great efforts have been dedicated to the ecological restoration of urban rivers around the world, as a solution to recovering the environmental functionality of these environments. In this sense, the present work aimed to investigate the effectiveness of interventions carried out aimed at the recovery of urban rivers, through a systematic review of the literature between 2010 and 2022, using the search term "rivers recovery." The results showed that there have been notable advances in the implementation of river recovery programs in urban areas around the world between the years analyzed. The ecosystems studied were affected, for the most part, by the increase in the supply of nutrients from domestic and industrial effluents, in addition to having highly urbanized surroundings and with several changes in land use patterns. The preparation of this literature review made it possible to demonstrate that the effectiveness of river recovery is extremely complex, since river recovery projects are developed for different reasons, as well as being carried out in different ways according to the intended objective.

Combining capillary electromigration with molecular imprinting techniques towards an optimal separation and determination.

Capillary electromigration is a well-established commercial group of analytical techniques, and, alike other column separation systems, it often benefits from a preceding sample preparation step. This step not only improves the analytical performance of many methods and prolongs the equipment's life span, but it also makes some determinations possible. A remarkable sample preparation technique is molecular imprinting technology: by creating tailored polymers able to 'select' the targeted analytes, matrix effects are severely diminished. This review aims to provide an overview of all the published works that combine capillary electrophoresis and molecularly imprinted polymers (MIP). Although a literature search produced around 130 published analytical methodologies and 5 patents, authors believe that there is still plenty of room for interesting developments. Works ranged from the analysis of pesticides to pharmaceuticals or hormones, being the most common instrumental detection spectrophotometric. The combination between MIP and electrophoresis can be divided into two main categories depending on where the MIPs are placed within the analytical 'pipeline': off-column and in-column. Off-column consisted of MIP batch application previous to capillary injection. In-column approaches are more complex, and can be divided into coating, monolith, packed (these three being considered capillary electrochromatography), and dispersed particles (affinity capillary electrophoresis).

Derivatizing assay for the determination of aldehydes using micellar electrokinetic chromatography.

In this work, the use of a novel derivatization agent for the determination of aldehydes (in this particular case: formaldehyde, acetaldehyde, propionaldehyde, and valeraldehyde) using micellar electrokinetic chromatography is reported. The derivatization reaction is based on the reaction of aldehydes with benzhydrazide to form the corresponding derivates with maximum absorbance at 250 nm. The experimental conditions of the derivatization reaction as well of the separation were optimized. The adducts were separated with a +22 kV voltage at a temperature of 29°C. The adducts' separation was performed in less than 14 min using as the running buffer a mixture containing 110 mmol/L of sodium dodecyl sulfate and 27 mmol/L of sodium tetraborate at pH 9.45. Samples were injected using hydrodynamic mode (50 mbar × 5 s). The calibration curves were linear up to 15.0 mg/L with r2 above 0.99. Intra and inter-day precisions were in average 3 and 4%, respectively, and recoveries were in average of 95%. Limits of detection and quantification were around 0.5 and 1.5 mg/L, respectively. The developed method was successfully applied in the analysis of low molar weight aldehydes in yogurt and vinegar samples.

Determination of 2-methylimidazole and 4-methylimidazole in caramel colors by capillary electrophoresis.

The use of chemical preservative compounds is common in the food products industry. Caramel color is the most usual additive used in beverages, desserts, and breads worldwide. During its fabrication process, 2- and 4-methylimidazole (MeI), highly carcinogenic compounds, are generated. In these cases, the development of reliable analytical methods for the monitoring of undesirable compounds is necessary. The primary procedure for the analysis of 2- and 4-MeI is using LC- or GC-MS techniques. These procedures are time-consuming and require large amounts of organic solvents and several pretreatment steps. This prevents the routine use of this procedure. This paper describes a rapid, efficient, and simple method using capillary electrophoresis (CE) for the separation and determination of 2- and 4-MeI in caramel colors. The analyses were performed using a 75 µm i.d. uncoated fused-silica capillary with an effective length of 40 cm and a running electrolyte consisting of 160 mmol L(-1) phosphate plus 30% acetonitrile. The pH was adjusted to 2.5 with triethylamine. The analytes were separated within 6 min at a voltage of 20 kV. Method validation revealed good repeatability of both migration time (<0.8% RSD) and peak area (<2% RSD). Analytical curves for 2- and 4-MeI were linear in the 0.4-40 mg L(-1) concentration interval. Detection limits were 0.16 mg L(-1) for 4-MeI and 0.22 mg L(-1) for 2-MeI. The extraction recoveries were satisfactory. The developed method showed many advantages when compared to the previously used method.

Laser-induced fluorescence and UV detection of derivatized aldehydes in air samples using capillary electrophoresis.

In this work, two capillary zone electrophoresis methodologies using UV absorption detection (214 nm) and laser-induced fluorescence detection (He/Cd laser, 325 nm excitation, 520 nm emission) of selected aldehydes (formaldehyde, acetaldehyde, propionaldehyde and acrolein) derivatized with dansylhydrazine (DNSH, 5-dimethylaminonaphthalene-1-sulfohydrazide) were proposed and validated. The aldehydes react with DNSH to form negatively charged molecules in methanolic medium. In both methodologies, nine DNSH-derivatives, including isomers of acetaldehyde, propionaldehyde and acrolein and two impurities were baseline separated in 20 mmol l(-1) phosphate buffer at pH 7.02, in less than 9 min. The limits of detection for the UV and LIF methodologies ranged from 1.1-9.5 microg l(-1) and 0.29-5.3 microg l(-1), respectively. The applicability of both methodologies to contemplate real samples was confirmed in the analysis of aldehyde-DNSH derivatives in indoor and outdoor air samples.