Semmens Michael J, Dahm Karl, Shanahan John, Christianson Alina
Department of Civil Engineering, University of Minnesota, Minneapolis, MN 55455, USA.
Water Res. 2003 Nov;37(18):4343-50. doi: 10.1016/S0043-1354(03)00416-0.
A bioreactor was constructed and used to treat a synthetic wastewater containing ammonium acetate and trace nutrients for about 190 days. The reactor was aerated by means of bundles of gas-permeable hollow-fiber membranes that were installed in the reactor. The membranes provided a specific surface area of 422 m(2)/m(3) and the external surface of the membranes rapidly became covered in an active biofilm. The membrane bundles were agitated by an internal gas recycle. The gas bubbles in the water encouraged fiber-fiber contact and were intended to control biofilm growth. Chemical oxygen demand (COD) removals in excess of 95% were achieved in a 6h nominal detention time. Nitrification developed rapidly and complete oxidation of the influent ammonium was evident within 20 days. Even though the reactor was equipped with a large membrane surface area, the oxygen was consumed within the biofilm growing on the membrane surface. As a result, the external dissolved oxygen (DO) dropped to zero and the reactor was able to support essentially complete denitrification. After about 3 months of operation the reactor showed excellent removals of both COD and inorganic nitrogen but the performance could not be sustained. Excess biofilm accumulation eventually contributed to a deterioration in process performance. This study demonstrates that while membrane aeration can provide simultaneous BOD and N removal in the same reactor, the membrane modules/bioreactor must be designed to allow for the development of thick biofilms. In addition, options for controlling the biofilm thickness need to be investigated.
构建了一个生物反应器,用于处理含醋酸铵和微量养分的合成废水约190天。该反应器通过安装在其中的透气中空纤维膜束进行曝气。这些膜提供了422平方米/立方米的比表面积,膜的外表面迅速被活性生物膜覆盖。膜束通过内部气体循环进行搅动。水中的气泡促进了纤维与纤维的接触,旨在控制生物膜的生长。在6小时的名义停留时间内,化学需氧量(COD)去除率超过95%。硝化作用迅速发展,进水铵在20天内明显实现了完全氧化。尽管反应器配备了较大的膜表面积,但氧气在膜表面生长的生物膜内被消耗。结果,外部溶解氧(DO)降至零,反应器能够支持基本完全的反硝化作用。运行约3个月后,反应器对COD和无机氮均表现出优异的去除效果,但该性能无法持续。过多的生物膜积累最终导致了工艺性能的恶化。本研究表明,虽然膜曝气可在同一反应器中同时去除BOD和氮,但膜组件/生物反应器的设计必须考虑到厚生物膜的形成。此外,需要研究控制生物膜厚度的方法。