Effects of Waste Activated Sludge Extracellular Polymeric Substances on Biosorption

Extracellular polymeric substances (EPS) reportedly make up approximately half of the organic matter in activated sludge (AS), and therefore strongly influence AS properties. This study evaluated the component fractions of EPS normalized to volatile suspended solids (VSS) in waste activated sludge (WAS) from a trickling-filter-solids contact process (TF/SC) and its ability to biosorb organic matter from raw wastewater with 30 min of contact time. Biosorption is the process in which organic matter (carbohydrates, proteins, humic acids, DNA, uronic acids, and lipids) in a sorbate, such as raw wastewater, sorbs onto a sorbent such as WAS. A statistically significant correlation was found between both the total concentration of EPS and the proteins component of the EPS and the biosorption removal of soluble chemical oxygen demand (sCOD) and truly soluble COD (ffCOD). Thus, the biosorption of soluble forms of COD can accurately be predicted by quantifying just the amount of proteins in WAS-associated EPS. No significant correlations were found for the biosorption of colloidal COD (cCOD). WAS biosorbed 45–75 mg L−1 of COD in 30 min. WAS absorbed or stored the proteins fraction of the soluble microbial products (SMP) during the biosorption process. Higher concentrations of humic acids were found in the biosorption process effluent than in the untreated wastewater, which warrants further study. Longer cation exchange resin (CER) extraction times yielded more total EPS from the sludge: 90 ± 9, 158 ± 3, and 316 ± 44 mg g−1 VSS, for 45-min, 4-h, and 24-h extraction times, respectively. Thus, EPS extracted represented only 9%, 15.8%, and 31.6% of the VSS, respectively, raising questions about whether the accurate characterization of EPS can be performed using the typical extraction time of 45 min due to different extraction rates for different components. It was found that the humic acids fraction was extracted much more slowly than the other fractions.

Ionophore-Based Potassium Selective Fluorescent Organosilica Nano-Optodes Containing Covalently Attached Solvatochromic Dyes

Fluorescent nanoprobes containing ionophores and solvatochromic dyes (SDs) were previously reported as an alternative to chromoionophore-based nano-optodes. However, the small-molecular SDs are prone to leakage and sequestration in complex samples. Here, we chemically attached the SDs to the surface of organosilica nanospheres through copper-catalyzed Click chemistry to prevent dye leakage. The nano-optodes remained well responsive to K+ even after exposure to a large amount of cation-exchange resin, which acted as a sink of the SDs. The potassium nanoprobes exhibited a dynamic range between 1 μM to 10 mM and a good selectivity thanks to valinomycin. Preliminary sensing device based on a nylon filter paper and agarose hydrogel was demonstrated. The results indicate that the covalent anchoring of SDs on nanospheres is promising for developing ionophore-based nanoprobes.

Synthesis of hydrated ferric oxide on cation exchange resin for phosphate and hardness removal in water

In this study, a potential adsorbent was synthesized from iron salt and cation exchange resin (FeOOH@CR) and applied for phosphate adsorption in batch experiments. The characteristics of FeOOH@CR materials before and after phosphate adsorption were determined by FTIR, XRD, and SEM. The factors affecting the adsorption process such as reaction time, solution pH, material dosage, concentration, temperature, and competing ions were tested. Kinetic, thermodynamic and isothermal models of the adsorption process were applied to study the nature of the adsorption process. The properties of phosphate adsorption, effect of competitive ions and material reusability were also examined. Results showed that the adsorption time reached equilibrium after 48 h and the suitable adsorption condition was found at solution pH of 6.5, material dosage of 5 g/L. In addition, the durability of the material after 5 times of regeneration was investigated with the remained adsorption ability of about 55% as compared to the original one.

FEATURES OF WATER TREATMENT FOR BOILER ROOMS

Thousands of medium and low steam boilers and hot water boilers operate in the country's industry, municipal energy and agriculture. Their reliable operation is largely determined by the maintenance of a rational water-chemical regime. The main problems of source water are the presence of dissolved oxygen, iron ions, salts of calcium, and magnesium. The aim of the work is to analyze the existing technologies and equipment for water treatment for different types of boilers. Determination of physicochemical parameters and requirements for source and prepared water. Presentation of new multi-purpose energy-efficient and resource-saving water treatment equipment. The article considers the negative impact of dissolved iron, hardness salts, dissolved gases present in the feed water on the operation of boiler equipment. The main requirements for feed water in terms of hardness, the content of dissolved oxygen, and oils for steam and hot water boilers are given. The mechanism of scale formation is given. The main existing methods of feed water treatment are considered, namely softening on Na-cation exchange resin, liming, softening, and reduction of total salt content on reverse osmosis units, softening, and reduction of total salt content by the sequential passage of water through H, OH-ion exchange filters. A multi-purpose aeration-oxidation setup of rotor type (AORT) is presented, which implements the method of discrete-pulse energy input, on which it is possible to carry out operations to remove iron, manganese, hardness salts, increase pH and degassing from water.

Isolation and radiochemical purification of samarium isotopes using ion exchange resins АВ 17×8 AND KU-2

The relevance of the research is caused by the need to develop a methodological base for determining 151Sm content in the soil cover of radioactively contaminated territories of Kazakhstan. The developed method for the determining of 151Sm will make it possible to assess the levels of soil contamination with this radionuclide, to determine the character of its spatial distribution, to allow estimating the internal exposure doses for the personnel and the population. The aim of the research is to carry out the isolation and radiochemical purification of samarium isotopes from acid solutions via using ion-exchange resins AV 17×8 and KU-2. Objects: salt solutions based on nitric and hydrochloric acid containing the stable isotopes of some natural, artificial β-emitters and isotopes of U and Th. The concentrations of nitric and hydrochloric acids were equal to the concentrations of the same acids used in the routine analysis of Pu and Am. Concentrations of chemical elements were determined using the Agilent 7700x quadrupole mass spectrometer and the iCAP 6300 Duo atomic emission spectrometer. The results of the experiments on the isolation and radiochemical purification of samarium isotopes from acidic solutions using anion-exchange resin AV 17×8 and cation-exchange resin KU-2 have been presented. It has been shown that the Sm-fraction can be purified from alkaline elements, Tl and U isotopes using the KU-2 cation-exchange resin. In turn, the isotopes U, Fe and Co can be removed using an anion exchange resin in 9M HCl media.

Formulation and evaluation of taste masked oral disintegrating tablets of lornoxicam

Orally disintegrating tablets (ODT) disintegrate quickly with saliva when administered into the oral cavity and taken without water or chewed. ODT are easy to take for children and the elderly, who may experience difficultly in taking ordinary oral preparations such as tablets, capsules, and powders. The ODT threes substantial benefits for the patient (or elder) who cannot swallow (Dysphagia), or who is not permitted water intake due to disease. The reason of the current research was to prepare taste masking oral disintegrating tablets of poorly soluble lornoxicam (LXM) by direct compression technique using Kyron T-114 (cation exchange resin) as a taste masking agent. With in various ratios the Drug-resin of 1:4 was established to present best taste masking. The superdisintegrants used in formulation are croscarmellose sodium and cross povidone. Among these croscarmellose sodium demonstrated superior drug release. The tablets were evaluated for friability, weight variation, wetting time, hardness, disintegration time and uniformity of content. Optimized formulations were evaluated for in vitro dissolution test. Amongst all the formulations F-6 was found to be most successful tablets prepared by this technique had disintegration time of 30sec and % CDR 94.78 within 30min. Hence, this advance can be utilized for taste masking of bitter pharmaceutical ingredients leading to superior patient compliance. Keywords: Oral disintegration tablets, Lornoxicam, Kyron T-114, Superdisintegrants, Direct Compression.

Assessing the Performance of Environmentally Friendly-Produced Zerovalent Iron Nanoparticles to Remove Pharmaceuticals from Water

Nano zerovalent iron (nZVI), produced from green tea extracts, was incorporated in a cation exchange resin (R-nFe) to investigate its performance regarding the removal of four non-steroidal anti-inflammatory drugs (NSAIDs): ibuprofen (IBU), naproxen (NPX), ketoprofen (KTP) and diclofenac (DCF). The effect of contact time, NaCl pretreatment, pH, R-nFe dose, the role of the supporting material, the initial concentration of pollutants, and the combined effect of nZVI with oxidative reagents was assessed through a series of batch experiments. According to the results, the best removal efficiencies obtained for DCF and KTP were 86% and 73%, respectively, at 48 h of contact time with NaCl pretreated R-nFe at a dose of 15 g L−1 and a pH of 4. The maximum removal efficiency for NPX was 90% for a contact time of 60 min with PS 1 mM and a pH of 3, which was quite similar to the experiment with a greater contact time of 48 h without PS addition. The maximum IBU removal was 70%; this was reached at pH 3, with a contact time of 30 min and R-nFe 15 g L−1. To the authors’ best knowledge, this is the first study investigating the utilization of nZVI, produced from leaf extracts and incorporated into a cationic exchange resin, to remove NSAIDs from water.

A Study of the Frequency Domain Induced Polarisation Effects Displayed by Clay and by Cation Exchange Resin, Model Soil Systems

<p>Work is reported of the development of clay and resin model soil systems for the observation of induced polarisation phenomena. A measuring technique is developed to determine impedance spectra of such models over the frequency range of 10-3 to 10 4 Hz, and a variety of model cells tested varying such parameters as temperature, electrolyte type and concentration, and bead size of resin. An increase in impedance with decrease in frequency is observed, consistent with field observation of the induced polarisation phenomenon associated with moist, non-mineralised soils, and a number of empirical observations of the form of this are made.</p>