WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

Permanent URI for this collectionhttps://hdl.handle.net/11147/7150

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  • Conference Object
    Citation - WoS: 24
    Effect of pH and Hydration on the Normal and Lateral Interaction Forces Between Alumina Surfaces
    (2006) Polat, Mehmet; Sato, Kimiyasu; Nagaoka, Takaaki; Watari, Koji
    Normal and lateral interaction forces between alumina surfaces were measured using Atomic Force Microscopy-Colloid Probe Method at different pH. The normal force curves exhibit a well-defined repulsive barrier and an attractive minimum at acidic pH and the DLVO theory shows excellent agreement with the data. The normal forces are always repulsive at basic pH and the theory fails to represent the measurements. Lateral forces are almost an order of magnitude smaller in the basic solutions. These differences, which have important implications in the study of stability and rheology, are attributed to the hydration of the alumina surface at basic pH. © 2013 Elsevier B.V., All rights reserved.
  • Conference Object
    Effect of Some Physical, and Chemical Variables on Flocculation and Sediment Behaviour
    (A.A. Balkema Publishers, 2000) Polat, Hürriyet; Polat, Mehmet; İpekoğlu, Üner
    Effect of some chemical and physical variables on the settling rate, final sediment height, sediment viscosity and supernatant turbidity of a clay sample was studied using various polyacrylamide type flocculants. Increasing flocculant concentration significantly increased both the settling rate and sediment viscosity. More importantly, changes in the final sediment, height, hence the packing density, was minimal for all the conditions tested once the sediment was allowed to consolidate. Also, the mode of addition of the polymer, at once or continuous, did not seem to affect any of the parameters measured. Conditioning time seemed to alter the settling rate at low polymer concentrations, but had no effect at high polymer concentrations. However, increasing the conditioning time caused a decrease in the sediment viscosity. Different types of the polyacrylimides generated different settling rates at a given concentration, but the final sediment height was nearly independent of polymer type.
  • Conference Object
    Citation - Scopus: 3
    Characterization of Polysulfone Based Hemodialysis Membranes by Afm
    (Elsevier Ltd., 2012) Uz, Metin; Yaşar Mahlıçlı, Filiz; Polat, Mehmet; Alsoy Altınkaya, Sacide
    Most of the hemodialysis membrane materials are hydrophobic in nature and allow protein adsorption on the surface easily due to hydrophobic interaction between membrane surface and protein molecules when in contact with blood. Adsorbed proteins can affect platelet and leukocyte adhesion, and modulate the response of plasmatic reactions followed by the activation of different defense systems in blood (Sun et al. 2003).
  • Article
    Citation - WoS: 98
    Citation - Scopus: 108
    Capacity and Mechanism of Phenol Adsorption on Lignite
    (Elsevier Ltd., 2006) Polat, Hürriyet; Molva, Murat; Polat, Mehmet
    A raw lignitic coal from Soma, Turkey was investigated to determine its potential as an adsorbent for phenol removal from wastewaters. Kinetic batch tests demonstrated that phenol could be completely removed from solution given sufficient solids loading and reaction time. The adsorption capacity of 10 mg/g obtained with the lignite is low compared to those achievable with activated carbons (around 300 mg/g). However, when normalized for the surface area, the adsorption capacity was much larger for the lignite (1.3 mg/m2) than that generally observed with activated carbons (0.05-0.3 mg/m2). Hydrogen-bonding of the phenolic -OH with the oxygen sites on the lignite surface is the most likely mechanism for adsorption. Though water molecules also have affinity for the same oxygen sites, lateral benzene ring interactions make phenol adsorption energetically more favorable. Since phenol molecules adsorbed in this fashion would project their benzene rings into solution, formation of a second layer through the action of the dispersive π-π interactions between the benzene rings is very likely. Residual water quality with respect to major elements and heavy metals was within acceptable limits defined by the ASTM standards. Dissolution of organic matter from the lignite was also observed to be negligible.
  • Article
    Citation - WoS: 198
    Citation - Scopus: 210
    Physical and Chemical Interactions in Coal Flotation
    (Elsevier Ltd., 2003) Polat, Mehmet; Polat, Hürriyet; Chander, Subhash
    Coal flotation is a complex process involving several phases (particles, oil droplets and air bubbles). These phases simultaneously interact with each other and with other species such as the molecules of a promoting reagent and dissolved ions in water. The physical and chemical interactions determine the outcome of the flotation process. Physical and chemical interactions between fine coal particles could lead to aggregation, especially for high rank coals. Non-selective particle aggregation could be said to be the main reason for the selectivity problems in coal flotation. It should be addressed by physical (conditioning) or chemical (promoters) pretreatment before or during flotation. Although the interactions between the oil droplets and coal particles are actually favored, stabilization of the oil droplets by small amounts of fine hydrophobic particles may lead to a decrease in selectivity and an increase in oil consumption. These problems could be remedied by use of promoters that modify the coal surface for suitable particle-particle, droplet-particle and particle-bubble contact while emulsifying the oil droplets. The role of promoters may be different for different types of coals, however. They could be employed as modifiers to increase the hydrophobicity of low rank coals whereas their main role might be emulsification and aggregation control for high rank coals. In this paper, a detailed description of the various phases in coal flotation, their physical and chemical interactions with each other in the flotation pulp, the major parameters that affect these interactions and how these interactions, in turn, influence the flotation process are discussed.