Chemistry / Kimya

Permanent URI for this collectionhttps://hdl.handle.net/11147/4072

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  • Article
    Citation - WoS: 123
    Citation - Scopus: 131
    A New Methodology for Removal of Boron From Water by Coal and Fly Ash
    (Elsevier Ltd., 2004) Polat, Hürriyet; Vengosh, Avner; Pankratov, Irena; Polat, Mehmet
    High levels of boron concentrations in water present a serious problem for domestic and agriculture utilizations. The recent EU drinking water directive defines an upper limit of 1 mgB/I. In addition, most crops are sensitive to boron levels >0.75 mg/1 in irrigation water. The boron problem is magnified by the partial (∼60%) removal of boron in reverse osmosis (RO) desalination due to the poor ionization of boric acid and the accumulation of boron in domestic sewage effluents. Moreover, high levels of boron are found in regional groundwater in some Mediterranean countries, which requires special treatment in order to meet the EU drinking water regulations. Previous attempts to remove boron employed boron-specific ion-exchange resin and several cycles of RO desalination under high pH conditions. Here, we present an alternative methodology for boron removal by using coal and fly ash as adsorbents. We conducted various column and batch experiments that explored the efficiency of boron removal from seawater and desalinated seawater using several types of coal and fly ash materials under controlled conditions (pH, liquid/solid ratio, time of reaction, pre-treatment, regeneration). We examined the effect of these factors on the boron removal capacity and the overall chemical composition of the residual seawater. The results show that the selected coal and fly ash materials are very effective in removing boron such that the rejection ratio of boron can reach 95% of the initial boron content under certain optimal conditions (e.g., pH = 9, L/S = 1/10, reaction time > 6 h). Our experiments demonstrated that use of glycerin enables regeneration of boron uptake into coal, but the boron uptake capacity of fly ash reduces after several cycles of treatment-reaction. The boron removal is associated with Mg depletion and Ca enrichment in the residual seawater and conversely with relative Mg enrichment and Ca depletion in the residual fly ash. We propose that the reaction of Ca-rich fly ash with Mg-rich seawater causes co-precipitation of magnesium hydroxide in which boron is co-precipitated. The new methodology might provide an alternative technique for boron removal in areas where coal and fly ash are abundant.
  • Article
    Citation - WoS: 39
    Citation - Scopus: 43
    Adsorption of Peo/Ppo Triblock Co-Polymers and Wetting of Coal
    (Elsevier Ltd., 1999) Polat, Hürriyet; Chander, Subhash
    The adsorption characteristics of PEO/PPO/PEO triblock co-polymers on coal were investigated using surface tension and contact angle measurements. Although these surfactants have been widely used as wetting agents, it was observed that they increased the hydrophobicity of coal at concentrations below about 10-6 M. Surface tension studies were carried out to explain the reasons for this behavior. The surface tension versus concentration profiles displayed three distinct regions. In region I, surface tension decreased linearly and monomers were proposed to be the dominant species. This region extended to a surfactant concentration of about 10-6 M. In region II, a transition region between regions I and III, dimers, trimers, etc., were considered to form. In region III, micelles formed and surface tension was independent of concentration. The concentration at which monomers associate to form dimers, etc., is referred to as the critical association concentration (cac). The contact angle of coal increased when concentration was raised from low values to the cac. It decreased when the reagent concentration was above the cac. Finally, at concentrations above the cmc, the wetting of coal was complete and contact angle was zero.
  • Article
    Citation - Scopus: 15
    Estimation of the Average Aromatic Cluster Size Based on Solid-State Nmr Measurement of Coal
    (Japan Institute of Energy, 1999) Kidena, Koh; Murata, Satoru; Artok, Levent; Nomura, Masakatsu
    Measurements of solid-state NMR of eight Argonne Premium Coal Samples were conducted to estimate the average aromatic cluster size in these coals. Firstly, the carbon distribution was obtained from SPE/MAS 13C-NMR. Secondary, 1H-CRAMPS NMR spectra gave the hydrogen aromaticity of coal. Combination use of the hydrogen aromaticity and elemental analysis data could afford the amount of tertiary aromatic carbon. The parameter of χ b, the mole fraction of aromatic bridgehead carbons in all aromatic carbons, could be derived from above NMR data and elemental analysis of coal. χ b is directly correlated to the number of aromatic carbon atoms per aromatic cluster, C. In this study, the value of C varied from 10 (corresponding to the size of naphthalene) for Beulah-Zap and Wyodak coals to 23 (corresponding to the size of coronene) for Pocahontas No. 3 coal.