Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection

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

Browse

Filters

2007 - 200912010 - 201912020 - 20241

Settings

Publication Index: search.filters.publicationIndex.PubMedSubject: search.filters.subject.Fly ash

Search Results

Now showing 1 - 3 of 3
  • Article
    Citation - WoS: 11
    Citation - Scopus: 11
    Renewable-Based Treatment Solution of Reactive Blue 21 Dye on Fly Ash as Low-Cost and Sustainable Adsorbent
    (Elsevier, 2024) Kobya, Mehmet; Dolaz, Mustafa; Goren, Aysegul Yagmur
    This study investigated the removal of Reactive Blue 21 (RB 21) dye from aqueous solutions by adsorption, evaluating the waste fly ash (FA). The effects of the parameters, such as initial dye concentration (100-750 mg/ L), initial pH (2.0-8.0), adsorbent dose (1.0-4.0 g/L), and temperature (298-323 K) on the adsorption process were investigated. The optimum initial pH value was 2.0 for the highest RB21 dye removal (75.2 mg/g). At optimized conditions (pH 2.0, an adsorbent dosage of 1.0 g/L, a dye concentration of 750 mg/L, and an equilibrium time of 72 h), the highest adsorption capacity was found to be 105.2 mg/g. Moreover, the results of the kinetic studies fitted the pseudo-second-order kinetic model. Equilibrium data were best represented by the Langmuir isotherm model, with a maximum monolayer adsorption capacity of 103.41 mg/g at 323 K. Delta G0ads values were negative and varied from 11.64 to 9.50 kJ/mol in the temperature range of 298-323 K, the values of enthalpy (Delta Ho ads) and entropy (Delta So ads) of thermodynamics parameters were calculated as 37.62 kJ/mol and 86.67 J/mol K, respectively, indicating that this process was endothermic. Furthermore, the adsorbent costs for powdered activated carbon (PAC) and FA to remove 1 kg of RB 21 dye from aqueous solutions are calculated as 2.52 U.S. $ and 0.34 U.S. $, respectively. It is seen that the cost of FA is approximately 7.4 times lower than PAC. The results showed that FA, a low-cost industrial waste, was promising for the adsorption of RB 21 from aqueous solutions.
  • Article
    Citation - WoS: 29
    Citation - Scopus: 38
    Encapsulating Fly Ash and Acidic Process Waste Water in Brick Structure
    (Elsevier Ltd., 2010) Köseoğlu, K.; Polat, Mehmet; Polat, Hürriyet
    Fly ash contains metals such as cadmium, iron, lead, aluminum and zinc in its structure in appreciable amounts. These metals can leach out into surface and ground waters if fly ash is not properly disposed of. A similar problem also exists for acidic process waste waters discharged by numerous industries. The purpose of this study was to utilize such wastes as additives in the production of construction quality bricks for the purpose of waste elimination. The bricks produced were subjected to flexural strength and water retention capacity tests along with heavy metal leaching experiments in order to determine the applicability of the procedure and the best possible recipes. This paper summarizes the results obtained in these tests along with the possible mechanisms involved in stabilizing the two wastes in the brick structure. © 2009 Elsevier B.V. All rights reserved.
  • Article
    Citation - WoS: 14
    Citation - Scopus: 15
    Neutralization of an Extremely Acidic Sludge and Stabilization of Heavy Metals in Flyash Aggregates
    (Elsevier Ltd., 2007) Polat, Mehmet; Güler, Erkan; Lederman, Eli; Cohen, Haim
    An extremely acidic, heavy metal-rich sludge (pH = -1.2) was scrubbed with a Class-F fly ash in order to simultaneously neutralize the acidity and stabilize the heavy metals contained in both wastes. This paper outlines the leaching behavior of the aggregate material generated by scrubbing. For proper fly ash/sludge ratios, the fly ash acted as an outstanding neutralizer for the acidic waste. Leaching of heavy metals from the aggregate samples was below the environmental limits within a pH range between 3 and 9. Subsequent washing of the leached aggregate with acidic CALWET solutions did not result in an additional release of heavy metals. It is proposed that coordinative bonding of the metal cations onto neutral surface sites and electrostatic adsorption led to stabilization of the heavy metals within the aggregate structure below hydrolysis pHs.