Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection

Permanent URI for this collectionhttps://hdl.handle.net/11147/7148

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Author: search.filters.author.Chander, SubhashInstitution Author: search.filters.institutionAuthor.Polat, Mehmet

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Now showing 1 - 3 of 3
  • 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.
  • Article
    Citation - WoS: 14
    Citation - Scopus: 22
    Characterization of Airborne Particles and Droplets: Relation To Amount of Airborne Dust and Dust Collection Efficiency
    (John Wiley and Sons Inc., 2002) Polat, Mehmet; Polat, Hürriyet; Chander, Subhash; Hogg, Richard
    Water sprays have been commonly used to suppress airborne dust. Water is doped with surface-active agents to enhance the dust capture efficiency through a reduction of surface tension. Nevertheless, dust collection efficiencies have been less than satisfactory historically. A detailed characterization of freshly generated airborne dust particles and spray droplets was carried out in order to explain this observation. Such properties as the agglomeration state of the freshly generated airborne dust particles and the airborne dust production capacity of various materials were defined and quantified. Electrostatic charges on individual airborne particles and spray droplets were measured. It was demonstrated that freshly generated airborne dust particles were extensively agglomerated. The magnitude of agglomeration was a function of material type and decided the amount of dust becoming airborne from a given material. This explains why certain materials such as quartz and anthracite produce more dust than some others. It was demonstrated that surfactants could be employed to charge the spray droplets selectively. The sign and magnitude of the droplet charge was a function of surfactant type and concentration. A strong correlation between the droplet charge and dust collection efficiencies by spray droplets was observed for cationic surfactants, suggesting that surfactants affected collection efficiency in addition to enhancing wetting.
  • Article
    Citation - WoS: 21
    Citation - Scopus: 24
    Kinetics of Oil Dispersion in the Absence and Presence of Block Copolymers
    (John Wiley and Sons Inc., 1999) Polat, Hürriyet; Polat, Mehmet; Chander, Subhash
    A phenomenological model proposed describes droplet breakup in the turbitlently agitated lean oil-in-water dispersions and provides a correlation between the median droplet size in an agitated vessel of standard geometry and the time of dispersion. It was assumed that the droplet breakup takes place in the dispersion-only region and coalescence is negligible. Vie model described the data from this study and the literature quite satisfactorily under these conditions. The effect of adding triblock PEO/PPO/PEO copofymeric surfactants on the dispersion kinetics of oil was also investigated. Addition of surfactant reduced the median oil droplet size significanfty, and the extent of this reduction was a strong function of surfactant concentration. Application of the model on these data demonstrated that the change in the median droplet size could be divided into two distinct regions. The breakage rate was high initially, most probably due to continuous adsorption of surfactant molecules at the oil/water interface. A lower breakage rate was attained at longer tunes, as the surfactant molecules were depleted from the solution. The time of transition bet\veen the t\vo was affected strongly by the concentration of the surfactant added. Furthermore, the time of addition of the surfactant did not affect the final droplet-size distribution in the system.