Grupo de Investigación en Remediación Ambiental y Biocatálisis (GIRAB), Instituto de Química, Facultad de Ciencias Exactas y Naturales, Universidad de Antioquia UdeA, Calle 70 No. 52-21, Medellín, Colombia.; Universidad Nacional de Colombia, Sede Medellín, Facultad de Minas, Departamento de Geociencias y Medioambiente, Colombia.
Environmental and Public Health Analytical Chemistry, Research Institute for Pesticides and Water, University Jaume I, Castelló, Spain.
Sci Total Environ. 2024 May 15;925:171625. doi: 10.1016/j.scitotenv.2024.171625. Epub 2024 Mar 11.
Catalytic ozonation using faujasite-type Y zeolite with two different SiO/AlO molar ratios (60 and 12) was evaluated for the first time in the removal of 25 pharmaceutical compounds (PhCs) present in real effluents from two municipal wastewater treatment plants both located in the Mediterranean coast of Spain. Additionally, control experiments including adsorption and direct ozonation, were conducted to better understand the fundamental aspects of the different individual systems in wastewater samples. Commercial zeolites were used in sodium form (NaY). The results showed that the simultaneous use of ozone and NaY zeolites significantly improved the micropollutants degradation rate, able to degrade 95 % of the total mixture of PhCs within the early 9 min using the zeolite NaY-12 (24.4 mg O L consumed), while 12 min of reaction with the zeolite NaY-60 (31 mg O L consumed). In the case of individual experiments, ozonation removed 95 % of the total mixture of PhCs after 25 min (46.2 mg O L consumed), while the direct adsorption, after 60 min of contact time, eliminated 30 % and 44 % using the NaY-12 and NaY-60 zeolites, respectively. Results showed that the Brønsted acid sites seemed to play an important role in the effectiveness of the treatment with ozone. Finally, the environmental assessment showed that the total risk quotients of pharmaceuticals were reduced between 87 %-99 % after ozonation in the presence of NaY-60 and NaY-12 zeolites. The results of this study demonstrate that catalytic ozonation using NaY zeolites as catalysts is a promising alternative for micropollutant elimination in real-world wastewater matrices.
首次使用两种不同 SiO/AlO 摩尔比(60 和 12)的丝光沸石进行催化臭氧化,以去除来自西班牙地中海沿岸两个城市污水处理厂的实际废水中存在的 25 种药物化合物(PhCs)。此外,还进行了包括吸附和直接臭氧化的对照实验,以更好地理解废水样品中不同单一系统的基本方面。商业沸石以钠离子形式(NaY)使用。结果表明,臭氧和 NaY 沸石的同时使用显著提高了微污染物的降解速率,在使用 NaY-12 沸石(消耗 24.4 mg O L)的情况下,在早期 9 分钟内就能降解总 PhC 混合物的 95%,而使用 NaY-60 沸石则需要 12 分钟(消耗 31 mg O L)。在单独实验的情况下,臭氧化在 25 分钟后去除了总 PhC 混合物的 95%(消耗 46.2 mg O L),而直接吸附在 60 分钟接触时间后,使用 NaY-12 和 NaY-60 沸石分别去除了 30%和 44%。结果表明,Brønsted 酸位似乎在臭氧处理的有效性中起着重要作用。最后,环境评估表明,在存在 NaY-60 和 NaY-12 沸石的情况下进行臭氧氧化后,药物的总风险商数降低了 87%-99%。本研究结果表明,使用 NaY 沸石作为催化剂的催化臭氧化是一种有前途的替代方法,可用于去除实际废水中的微污染物。