Kinetic study of adsorption and photo-decolorization of Reactive Red 198 on TiO2 surface

Recycling and reuse of wastewater after purification will reduce the environmental pollution as well as fulfill the increasing demand of water. Adsorption-based water treatment process is very popular for dye-house wastewater treatment. The present study deals with treatment of wastewater contaminated by reactive dye. TiO2 is used as adsorbent and the spent adsorbent has been regenerated by Advanced Oxidation Process (AOP), without using any other chemicals. TiO2 adsorbs dye molecules and then those dye molecules have been oxidized via a photocatalytic reaction in presence of UV irradiation. Kinetics of dye adsorption and photocatalytic oxidation reaction has been developed in this study. Photocatalyst adsorbent (TiO2) has been reused several times after regeneration. The activity of catalyst decreases after each cycle; due to poisoning cause by intermediate by-products. Kinetic of this catalyst deactivation has been incorporated with L–H model to develop the photocatalytic reaction kinetic model

Effect of Major Ions on Induction Time of Struvite Precipitation

Struvite precipitation from wastewaters has gained importance as a means of nitrogen and phosphorus treatment and recovery. While the aspects of process modeling and application have been widely studied, little attention was paid to process kinetics. This study attempted to evaluate the induction time of struvite precipitation for low ammonia concentrations and in the presence of ions commonly found in natural waters. Determination of induction time was based on absorbance measurements while conductivity and pH of the solutions were also monitored during the process. Results of the experimental study indicate that the presence of foreign ions is important in determining the induction time along with the degree of supersaturation. The presence of over 50 x 10–3 mol dm–3 sodium ions retarded induction time significantly. Calcium ions at 2.5 x 10–4 mol dm–3 concentration caused no marked change in the induction time. While carbonate ions had a slight effect, sulfate ions increased the induction time. Crystal morphology was also observed to be affected by supersaturation and the presence of foreign ions

A model for predicting dissolved organic carbon distribution in a reservoir water using fluorescence spectroscopy

A number of water treatment works (WTW) in the north of England (UK) have experienced problems in reducing the dissolved organic carbon (DOC) present in the water to a sufficiently low level. The problems are experienced in autumn/ winter when the colour increases and the coagulant dose at the WTW needs to be increased in order to achieve sufficient colour removal. However, the DOC content of the water varies little throughout the year. To investigate this further, the water was fractionated using resin adsorption techniques into its hydrophobic (fulvic and humic acid fractions) and hydrophilic (acid and non-acid fractions) components. The fractionation process yields useful information on the changing concentration of each fraction but is time consuming and labour intensive. Here, a method of rapidly determining fraction concentration was developed using fluorescence spectroscopy. The model created used synchronous spectra of fractionated material compared against bulk water spectra and predicted the fraction concentrations to within 10% for a specific water. The model was unable to predict fraction concentrations for waters from a different watershed

Spatial Natural Language Generation for Location Description in Photo Captions

We present a spatial natural language generation system to create captions that describe the geographical context of geo-referenced photos. An analysis of existing photo captions was used to design templates representing typical caption language patterns, while the results of human subject experiments were used to create field-based spatial models of the applicability of some commonly used spatial prepositions. The language templates are instantiated with geo-data retrieved from the vicinity of the photo locations. A human subject evaluation was used to validate and to improve the spatial language generation procedure, examples of the results of which are presented in the paper

Salicylaldehyde hydrazones: buttressing of outer sphere hydrogen-bonding and copper-extraction properties

Salicylaldehyde hydrazones are weaker copper extractants than their oxime derivatives, which are used in hydrometallurgical processes to recover ~20 % of the world’s copper. Their strength, based on the extraction equilibrium constant Ke, can be increased by nearly three orders of magnitude by incorporating electron-withdrawing or hydrogen-bond acceptor groups (X) ortho to the phenolic OH group of the salicylaldehyde unit. Density functional theory calculations suggest that the effects of the 3-X substituents arise from a combination of their influence on the acidity of the phenol in the pH-dependent equilibrium, Cu2+ + 2Lorg ⇌ [Cu(L–H)2]org + 2H+, and on their ability to ‘buttress’ interligand hydrogen bonding by interacting with the hydrazone N–H donor group. X-ray crystal structure determination and computed structures indicate that in both the solid state and the gas phase, coordinated hydrazone groups are less planar than coordinated oximes and this has an adverse effect on intramolecular hydrogen-bond formation to the neighbouring phenolate oxygen atoms

Strings in extremal BTZ black holes

We study the spectrum of the worldsheet theory of the bosonic closed string in the massless and extremal rotating BTZ black holes. We use a hyperbolic Wakimoto representation of the SL(2,R) currents to construct vertex operators for the string modes on these backgrounds. We argue that there are tachyons in the twisted sector, but these are not localised near the horizon. We study the relation to the null orbifold in the limit of vanishing cosmological constant. We also discuss the problem of extending this analysis to the supersymmetric case.Comment: 20 pages, no figure

3-Fluoro­salicylaldoxime at 6.5 GPa

3-Fluoro­salicylaldoxime, C7H6FNO2, unlike many salicylaldoxime derivatives, forms a crystal structure containing hydrogen-bonded chains rather than centrosymmetric hydrogen-bonded ring motifs. Each chain inter­acts with two chains above and two chains below via π–π stacking contacts [shortest centroid–centroid distance = 3.295 (1) Å]. This structure at 6.5 GPa represents the final point in a single-crystal compression study