REAL TIME SUPERVISION OF WASTEWATER TREATMENT PLANTS: A DISTRIBUTED AI APPROACH

Author(s):  
M. SÀNCHEZ ◽  
L. R-RODA ◽  
J. LAFUENTE ◽  
U. CORTÉS ◽  
M. POCH
1994 ◽  
Vol 27 (10) ◽  
pp. 188-193
Author(s):  
M. Sànchez ◽  
L. R-Roda ◽  
J. Lafuente ◽  
U. Cortés ◽  
M. Poch

2020 ◽  
Vol 721 ◽  
pp. 137629 ◽  
Author(s):  
Jiang-han Tian ◽  
Cheng Yan ◽  
Zaheer Ahmad Nasir ◽  
Sonia Garcia Alcega ◽  
Sean Tyrrel ◽  
...  

2002 ◽  
Vol 46 (1-2) ◽  
pp. 267-272 ◽  
Author(s):  
S.J. Hall ◽  
P. Hugenholtz ◽  
N. Siyambalapitiya ◽  
J. Keller ◽  
L.L. Blackall

Chemical analytical data has long been used to monitor the performance of activated sludge plants even though the process relies on the performance of microorganisms. It is now evident that a rapid and reliable quantitative method is required, to be able to monitor the organisms responsible for nutrient transformation and their activities, allowing avenues for more efficient nutrient removal. The development of real-time or quantitative polymerase chain reaction (PCR) also known as TaqMan® or 5′-nuclease assay has allowed the rapid, quantitative analysis of DNA templates, eliminating some of the variability traditionally associated with other quantitative techniques. In this study analysis of Nitrospira spp., one of the key organisms in nitrite oxidation in wastewater treatment, was used to validate real-time PCR for the their quantification in activated sludge. A probe and primer set, targeting the 16S rRNA gene of Nitrospira spp. was designed according to the constraints of the TaqMan® specifications. Samples used to evaluate the method included DNA from the sludge from full-scale wastewater treatment plants and laboratory scale systems. The reproducibility, quantitative efficiency and specificity were assessed in the evaluation. It was concluded that the method is sensitive and reproducible but has some constraints on the quantitative efficiency. A survey of full-scale systems for Nitrospira spp. was carried out and the results are presented here.


2012 ◽  
Vol 66 (10) ◽  
pp. 2065-2073 ◽  
Author(s):  
N. Yokomachi ◽  
J. Yaguchi

A photo-inducible DNA-binding dye, propidium monoazide (PMA), was used to distinguish viable and dead Escherichia coli cells. Microscopic observations using a combination of the dyes 4′,6-diamidino-2-phenylindole and PMA indicated that PMA stained only dead cells, with membrane damage, red. Mixtures of viable and heat-treated E. coli cells were subjected to real-time polymerase chain reaction (PCR) with PMA treatment. Viable cell counts were linearly related to real-time PCR threshold cycle values for PMA-treated cells in the mixtures of viable and heat-treated cells, as long as the ratio of dead cells to viable cells was no greater than 10. In the wastewater treatment plants, total, viable and culturable E. coli were enumerated by real-time PCR, real-time PCR coupled with PMA treatment and the most probable number method using EC-MUG medium, respectively. The concentrations of viable E. coli in the wastewater treatment plants were much higher than those of culturable cells. In addition, viable cells were even more chlorine resistant than culturable ones.


Sign in / Sign up

Export Citation Format

Share Document