Department of Chemical and Materials Engineering, University of Kentucky , 177 F. Paul Anderson Tower, Lexington, Kentucky 40506, United States.
ACS Appl Mater Interfaces. 2017 May 3;9(17):14858-14867. doi: 10.1021/acsami.7b01999. Epub 2017 Apr 21.
Functionalized membranes provide versatile platforms for the incorporation of biocatalysts and nanostructured materials for efficient and benign environmental remediation. The existing techniques for remediating chloro-organics in water consist of both physical and chemical means mostly using metal oxide-based catalysts, despite associated environmental concerns. To offer bioinspired remediation as an alternative, we herein demonstrate a layer-by-layer approach to immobilize laccase enzyme onto pH-responsive functionalized membranes for the degradation of chloro-organics in water. The efficacy of these bioinspired membranes toward dechlorination of 2,4,6-trichlorophenol (TCP) is demonstrated under a pressure-driven continuous flow mode (convective flow) for the first time to the best of our knowledge. Over 80% of the initial TCP was degraded at an optimum flow rate under an applied air pressure of about 0.7 bar or lower. This corresponds to degradation of a substantial amount of the initial substrate in only 36 s residence time, whereas it takes hours for degradation in a batch reaction. This, in fact, demonstrates an energy efficient flow-through system with potentially large-scale applications. Comparison of the stability of the enzyme in the solution phase versus immobilized on the membrane phase showed a loss of some 65% of enzyme activity in the solution phase after 22 d, whereas the membrane-bound enzyme lost only a negligible percentage of the activity in a comparable time span. Finally, the membrane was exposed to rigorous cycles of TCP degradation trials to study its reusability. The primary results reveal a loss of only 14% of the initial activity after 4 cycles of use in a period of 25 d, demonstrating its potential to be reused. Regeneration of the functionalized membrane was also validated by dislodging the immobilized enzyme, followed by immobilization of fresh enzyme onto the membrane.
功能化膜为生物催化剂和纳米结构材料的纳入提供了多功能平台,可实现高效、良性的环境修复。现有的水相氯代有机物修复技术包括物理和化学方法,主要使用基于金属氧化物的催化剂,但存在相关的环境问题。为了提供生物启发的修复方法作为替代方法,我们在此展示了一种逐层方法,将漆酶酶固定在 pH 响应功能化膜上,用于水中氯代有机物的降解。据我们所知,这是首次在压力驱动连续流动模式(对流)下证明这些仿生膜对 2,4,6-三氯苯酚(TCP)脱氯的有效性。在约 0.7 巴或更低的施加空气压力下,在最佳流速下,初始 TCP 的 80%以上被降解。这相当于在仅 36 秒的停留时间内降解了相当数量的初始底物,而在分批反应中则需要数小时。实际上,这展示了一种节能的大通量系统,具有潜在的大规模应用前景。将酶在溶液相中的稳定性与在膜相中的固定进行比较表明,在溶液相中,酶活性在 22 天后损失了约 65%,而在可比时间内,膜结合酶的活性仅损失了微不足道的百分比。最后,该膜经受了严格的 TCP 降解试验循环,以研究其可重复使用性。主要结果表明,在 25 天的 4 个使用周期后,初始活性仅损失 14%,表明其具有重复使用的潜力。通过去除固定化酶并将新鲜酶固定在膜上,也验证了功能化膜的再生。