Effect of influent nutrient ratios and hydraulic retention time (HRT) on simultaneous phosphorus and nitrogen removal in a two-sludge sequencing batch reactor process

A laboratory-scale anaerobic–anoxic/nitrification sequencing batch reactor (A2N- SBR) fed with domestic wastewater was operated to examine the effect of varying ratios of influent COD/P, COD/TN and TN/P on the nutrient removal. With the increased COD/P, the phosphorus removals exhibited an upward trend. The influent TN/P ratios had a positive linear correlation with the phosphorus removal efficiencies, mainly because nitrates act as electron acceptors for the phosphorus uptake in the A2N-SBR. Moreover, it was found that lower COD/TN ratio, e.g. 3.5, did not significantly weaken the phosphorus removal, though the nitrogen removal first decreased greatly. The optimal phosphorus and nitrogen removals of 94% and 91%, respectively were achieved with influent COD/P and COD/ TN ratios of 19.9 and 9.9, respectively. Additionally, a real-time control strategy for A2N-SBR can be undertaken based on some characteristic points of pH, redox potential (ORP) and dissolved oxygen (DO) profiles in order to obtain the optimum hydraulic retention time (HRT) and improve the operating reliabili

Optical absorption and electrical conductivity of electron acceptor doped poly-3-octylthiophene films

Optical absorption and electrical conductivity measurements of solution-doped poly-3-octylthiophene (P3OT) films were studied. Chloroform solutions of P3OT were doped with the organic electron-acceptors, 2,3-dichloro-5,6-dicyano-l,4-benzoquinone (DDQ) and 7,7,8,8-tetracyanoquinodimethane (TCNQ); and with the inorganic electron acceptor, ferric chloride (FeCl{dollar}\sb3{dollar}). Charge transfer was observed in P3OT solutions doped with FeCl{dollar}\sb3{dollar} and DDQ. TCNQ-doped solutions showed no optical evidence of charge transfer. Thin films of the doped P3OT were examined at various doping levels. Spectroscopic and electrical conductivity measurements of P3OT films, doped with DDQ, TCNQ, and FeCl{dollar}\sb3{dollar}, at different doping levels, are presented. Optical absorption measurements provided information on the degree of charge transfer occurring for the various dopants. Electrical conductivity measurements showed that the conductivity of P3OT increased with the various dopants in the order of TCNQ {dollar}\u3c{dollar} DDQ {dollar}\u3c{dollar} FeCl{dollar}\sb3{dollar}, for the same dopant concentration level. Results are discussed in relation to the electrochemical properties of the prepared films and the structural properties of P3OT

Open Notebook Science Challenge: Solubilities of Organic Compounds in Organic Solvents

This book contains the results of the Open Notebook Science Solubility Challenge. All experimental measurements are provided with a link to either the laboratory notebook page where the experiment was carried out or to a literature reference. The Challenge was sponsored by Submeta, Nature and Sigma-Aldrich

Open Notebook Science Challenge: Solubilities of Organic Compounds in Organic Solvents

This book contains the results of the Open Notebook Science Solubility Challenge. All experimental measurements are provided with a link to either the laboratory notebook page where the experiment was carried out or to a literature reference. The Challenge was sponsored by Submeta, Nature and Sigma-Aldrich

Energy-harvesting materials

It is shown how key features of natural photosynthesis can be emulated in novel materials based on photoactive multichromophore arrays and crystals. A major consideration in the design of such systems is the means of channeling electronic excitation from sites of light absorption to centers where it is stored or released. Storage is often achieved by driving charge separation or, for the longer term, a more complex chemical reaction whilst rapid release is commonly associated with frequency up-converted emission. In each case channeling to the conversion site generally entails a multi-step energy transfer mechanism whose efficiency is determined by the arrangement and electronic properties of the array chromophores or ions, guided in the more complex systems by a spectroscopic gradient that promotes overall directionality. The functional cascade molecules known as photoactive dendrimers are exemplars of this approach. The latest developments involve new mechanisms for concerted excitation transfer in multichromophore systems, leading towards the tailoring and exploitation of optical nonlinearities for high intensity energy pooling applications