Mono and bimetallic Mn–Fe catalysts supported on different materials were prepared and their catalytic performance in the NH3–SCR of NOx was investigated. It was shown that Mn and Fe have a synergic effect that enhances the activity at low temperature. Nevertheless, the activity of the bimetallic catalysts depends very much on the support selected. The influence of the support on the catalyst activity has been studied using materials with different textural and acid–base properties. Microporous (BEA-zeolite), mesoporous (SBA15 and MCM41) and bulk (metallic oxides) materials with different acidity have been used as supports for the Mn–Fe catalysts. It has been shown that the activity depends on the acidity of the support and on the surface area. Acid sites are necessary for ammonia adsorption and high surface area produces a better dispersion of the active sites resulting in improved redox properties. The best results have been obtained with the catalysts supported on alumina and on beta zeolite. The first one is the most active at low temperatures but it presents some reversible deactivation in the presence of water. The Mn–Fe catalyst supported on beta zeolite is the most active at temperatures higher than 350 °C, without any deactivation in the presence of water and with a 100% selectivity towards nitrogen.
The presence of illicit discharges in sewerage systems generates an important impact in wastewater treatment plants and the ecosystem. In this paper, we present two prototypes for monitoring the presence of solids in wastewater and to study the effect of the water height. The prototypes are based on color and infrared LEDs and two photosensors located in the prototypes at 0° and 180° degrees. When the photosensor is located at 180°, all color LEDs present a good range of output voltage (approximately 5 V to 0 V) and good R2. However, for the typical concentration of solids in wastewater, the prototypes do not work correctly. When the photosensor is located in the prototypes the LEDs, yellow, red, and white have a good operation with voltage differences of 1.73 V, 1.76 V, and 1.13 V in P1 and 1.58 V, 1.84 V, and 1.35 V in P2, respectively. We calculate the mathematical model with the heights and solid concentration. The mathematical models which do not consider height present good R2. In conclusion, when the photosensor is located in the prototype, the height does not have an important effect and can detect the illicit discharge of solids. When the photosensor is located at 180°, it can be used for water with important changes in solid concentrations.
The deterioration of freshwater ecosystems in anthropogenic wetlands is intensified due to phosphorus inputs from fertilizers applied in agricultural areas. In addition, managing the excess green waste generated in these ecosystems increases the complexity of the problem. To move towards a sustainable society based on the circular economy, the use of controlled combustion of green waste to obtain bioenergy—followed by the application of the resulting ash for phosphorus removal from freshwater bodies via adsorption processes—should be considered. Furthermore, those ashes could be used as natural fertilizers and incorporated into the cultivated fields. This paper presents a deep study of the adsorption of phosphorus ions using ashes from the main green waste produced in wetlands. Various experiments were conducted to determine the effects of different variables in the removal process. A double kinetic model was necessary to explain the presence of two different removal processes. The Langmuir model described the equilibrium isotherm data of both adsorbents through an endothermic process. Acidic pH in the initial solutions was preferred because it promotes phosphorus removal by calcium dissolution. The alkalinity did not have a substantial effect on the adsorbent capacity. Calcium was the element that had a more significant influence on the overall process. Finally, a removal study using blended materials was performed. A combined model was proposed and validated based on the original isotherm models for the pure materials.