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Monitoring aerobic sludge digestion by online scanning fluorometry

机译:在线扫描荧光法监测好氧污泥的消化

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With sludge samples from two wastewater treatment plants, batch experiments of aerobic sludge digestion were conducted under different dissolved oxygen (DO) and solids concentrations. A fluorometer capable of online excitation and emission scanning was used to monitor the digestion process. Three major fluorescence peaks were observed. The peak at excitation/emission maxima of 290/350 nm was attributed to the fluorescence of proteinaceous materials in the sludge, with tryptophan residues being the primary contributor. The sources for the other two peaks (at 370/430 nm and 430/510 nm) remain unknown. The well-known biological fluorescence from reduced nicotinamide adenine dinucleotides (NADH and NADPH), at excitation/emission maxima of 340/460 nm, was found very weak in the aerobic digestion systems studied. It was buried under the broad peak at 370/430 nm and was detectable only in the early stage of the experiment that had the highest solids loading (at 4.8%) and was operated under low DO (0.2-1.0 mg/L) conditions. On the other hand, the profile of the protein fluorescence (PF) correlated well with that of the volatile solids (VS) reduction in all the experiments. A semi-empirical exponential decay function was developed, which described well the profiles of both normalized VS and normalized PF. The feasibility of following the real-time performance of aerobic sludge digestion by monitoring PF was clearly demonstrated.
机译:对于来自两个废水处理厂的污泥样品,在不同的溶解氧(DO)和固体浓度下进行了好氧污泥消化的分批实验。使用能够在线激发和发射扫描的荧光计来监测消化过程。观察到三个主要的荧光峰。激发/发射最大值为290/350 nm时的峰归因于污泥中蛋白质物质的荧光,色氨酸残基是主要贡献者。其他两个峰值(在370/430 nm和430/510 nm处)的来源仍然未知。在所研究的需氧消化系统中,发现最大的激发/发射波长为340/460 nm时,还原的烟酰胺腺嘌呤二核苷酸(NADH和NADPH)产生的众所周知的生物荧光非常弱。它被掩埋在370/430 nm的宽峰下,并且仅在实验的早期阶段才可检测到,该阶段具有最高的固形物载量(4.8%)并且在低DO(0.2-1.0 mg / L)条件下运行。另一方面,在所有实验中,蛋白质荧光(PF)的分布与挥发性固体(VS)还原的分布密切相关。建立了半经验指数衰减函数,该函数很好地描述了归一化VS和归一化PF的轮廓。通过监测PF来跟踪好氧污泥消化的实时性能的可行性已得到明确证明。

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