Gómez Elvira, Fons Arnau, Cestaro Roberto, Serrà Albert
Grup d'Electrodeposició de Capes Primes i Nanoestructures (GE-CPN), Departament de Ciència de Materials i Química Física, Universitat de Barcelona, Martí i Franquès, 1, 08028 Barcelona, Catalonia, Spain.
Institute of Nanoscience and Nanotechnology (IN2UB), Universitat de Barcelona, 08028 Barcelona, Catalonia, Spain.
Nanomaterials (Basel). 2023 Feb 21;13(5):790. doi: 10.3390/nano13050790.
Synthesizing efficient heterogeneous catalysts with multiple active sites able to activate peroxymonosulfate (PMS) for the degradation of persistent organic pollutants continues to be a challenge for societies worldwide. In response, cost-effective, eco-friendly oxidized Ni-rich and Co-rich CoNi micro-nanostructured films were fabricated following a two-step process based on simple electrodeposition using green deep eutectic solvent as an electrochemical media and thermal annealing. The CoNi-based catalysts demonstrated exceptional efficiency in the heterogeneous catalyzed activation of PMS for tetracycline degradation and mineralization. The effects of the catalysts' chemical nature and morphology, the pH, the concentration of PMS, irradiation with visible light, and the duration of contact with the catalysts on the degradation and mineralization of tetracycline were also studied. In dark conditions, oxidized Co-rich CoNi degraded more than 99% of tetracyclines in only 30 min and mineralized more than 99% of them in only 60 min. Moreover, the degradation kinetics doubled from 0.173 min in dark conditions to 0.388 min under visible light irradiation. In addition, the material demonstrated excellent reusability and can be easily recovered with simple heat treatment. Given those findings, our work provides new strategies for constructing high-efficiency and cost-effective PMS catalysts and elucidating the effects of operational parameters and primary reactive species formed by the catalyst-PMS system on water treatment technologies.
合成具有多个活性位点、能够激活过一硫酸盐(PMS)以降解持久性有机污染物的高效非均相催化剂,仍然是全球社会面临的一项挑战。作为回应,采用两步法,以绿色深共熔溶剂作为电化学介质并通过简单电沉积和热退火,制备了具有成本效益且环保的富镍和富钴氧化型CoNi微纳结构薄膜。基于CoNi的催化剂在非均相催化激活PMS以降解四环素和使其矿化方面表现出卓越的效率。还研究了催化剂的化学性质和形态、pH值、PMS浓度、可见光照射以及与催化剂接触的持续时间对四环素降解和矿化的影响。在黑暗条件下,富钴氧化型CoNi在仅30分钟内就能降解超过99%的四环素,并在仅60分钟内使其矿化超过99%。此外,降解动力学从黑暗条件下的0.173分钟增加到可见光照射下的0.388分钟。此外,该材料表现出优异的可重复使用性,并且通过简单的热处理就能轻松回收。鉴于这些发现,我们的工作为构建高效且具有成本效益的PMS催化剂以及阐明操作参数和催化剂 - PMS系统形成的主要活性物种对水处理技术的影响提供了新策略。