Taboada-Puig Roberto, Lu-Chau Thelmo A, Eibes Gemma, Feijoo Gumersindo, Moreira Maria T, Lema Juan M
Dept. Chemical Engineering, Inst. of Technology, University of Santiago de Compostela, 15782, Spain.
Biotechnol Prog. 2015 Jul-Aug;31(4):908-16. doi: 10.1002/btpr.2116. Epub 2015 Jun 14.
The oxidant Mn(3+) -malonate, generated by the ligninolytic enzyme versatile peroxidase in a two-stage system, was used for the continuous removal of endocrine disrupting compounds (EDCs) from synthetic and real wastewaters. One plasticizer (bisphenol-A), one bactericide (triclosan) and three estrogenic compounds (estrone, 17β-estradiol, and 17α-ethinylestradiol) were removed from wastewater at degradation rates in the range of 28-58 µg/L·min, with low enzyme inactivation. First, the optimization of three main parameters affecting the generation of Mn(3+) -malonate (hydraulic retention time as well as Na-malonate and H2 O2 feeding rates) was conducted following a response surface methodology (RSM). Under optimal conditions, the degradation of the EDCs was proven at high (1.3-8.8 mg/L) and environmental (1.2-6.1 µg/L) concentrations. Finally, when the two-stage system was compared with a conventional enzymatic membrane reactor (EMR) using the same enzyme, a 14-fold increase of the removal efficiency was observed. At the same time, operational problems found during EDCs removal in the EMR system (e.g., clogging of the membrane and enzyme inactivation) were avoided by physically separating the stages of complex formation and pollutant oxidation, allowing the system to be operated for a longer period (∼8 h). This study demonstrates the feasibility of the two-stage enzymatic system for removing EDCs both at high and environmental concentrations.
木质素分解酶通用过氧化物酶在两阶段系统中产生的氧化剂Mn(3+)-丙二酸酯,被用于从合成废水和实际废水中连续去除内分泌干扰化合物(EDCs)。一种增塑剂(双酚A)、一种杀菌剂(三氯生)和三种雌激素化合物(雌酮、17β-雌二醇和17α-乙炔雌二醇)以28-58 μg/L·min的降解速率从废水中被去除,且酶失活程度较低。首先,按照响应面法(RSM)对影响Mn(3+)-丙二酸酯生成的三个主要参数(水力停留时间以及丙二酸钠和过氧化氢的进料速率)进行了优化。在最佳条件下,证明了在高浓度(1.3-8.8 mg/L)和环境浓度(1.2-6.1 μg/L)下EDCs的降解情况。最后,当将该两阶段系统与使用相同酶的传统酶膜反应器(EMR)进行比较时,观察到去除效率提高了14倍。同时,通过将络合物形成阶段和污染物氧化阶段进行物理分离,避免了在EMR系统中去除EDCs过程中发现的操作问题(例如膜堵塞和酶失活),使系统能够运行更长时间(约8小时)。这项研究证明了该两阶段酶系统在高浓度和环境浓度下去除EDCs的可行性。