Ahmet Sarı

Response surface optimization, kinetic and thermodynamic studies for effective removal of rhodamine B by magnetic AC/CeO2 nanocomposite

The activated carbon (AC) was obtained from waste scrap tires and modified by bimetallic Fe and Ce nanoparticles in order to combine both the high surface area and the active sites for enhanced adsorption of the dye. The produced nanocomposite was used as a novel cost-effective magnetic in rhodamine B (RhB) removal from aqueous solutions. The FT-IR, SEM, EDX, TEM, and surface area analysis methods were implemented to characterize the morphological, chemical, thermal and surface properties of the developed adsorbent. The optimum batch experimental conditions were found under the response surface methodology. The adsorption equilibrium data were well fitted by the Langmuir isotherm model. The adsorption capacity was 324.6xa0mgxa0g-1. The kinetic and thermodynamics studies were also carried out to understand the adsorption mechanism. The study indicated that RhB adsorption by the AC/Fe/Ce magnetic adsorbent has an endothermic character and followed the pseudo-second-order kinetics model. By using ethanol solution, RhB was desorbed at high efficiency and the prepared material could be recycled for up to ten cycles. Thus, the magnetic nanocomposite is an effective and promising adsorbent for the cleaning treatment of RhB ions from wastewater by a large scale designed adsorption system.

Polyamide magnetic palygorskite for the simultaneous removal of Hg(II) and methyl mercury; with factorial design analysis

A novel efficient adsorbent was prepared by the modification of magnetic palygorskite (MPG) by polyamide via the interfacial polymerization of trimesoyl chloride with m-phenylenediamine. The prepared magnetic palygorskite modified with polyamide (MPGP) material was appraised for its removal of the Hg(II) and CH3Hg species from aqueous solutions. The developed adsorbent was characterized using spectroscopic techniques. The adsorption ability of the MPGP sorbent was systematically investigated by using the batch method. Factorial design analysis was applied to study the effect of different batch parameters on the adsorption yield of both mercury species. These factors include mercury concentration, initial pH, sorbent amount and contact time. The equilibrium data coincided with the Langmuir adsorption isotherm indicating the maximum adsorption capacity of the MPGP was determined as 211.93u202fmg/g for Hg(II) and 159.73u202fmg/g for CH3Hg. The kinetic mechanism of the adsorption of both mercury species was well defined by the pseudo-second-order while the adsorption processes demonstrated spontaneity and an exothermic character at the studied temperatures. The cycling adsorption/desorption tests made by using a 1u202fmol/L HCl solution demonstrated that the MPGP had good reusable performance up to seven cycles. Based on the results it can be suggested that the synthesized MPGP sorbent can be handled for the elimination of Hg(II) and CH3Hg from wastewater effluents.

Applications of Thermal Analysis to the Study of Phase-Change Materials

Abstract To standardize the phase-change materials (PCMs) with regard to their thermophysical and thermal energy storage (TES) properties for achieving better heat storage performance in real-time applications, the greater emphasis being shown on the methods of thermal analysis are increasingly attractive, in recent years. This has paved way for gleaning of the technical revelations from a variety of research studies and is highlighted throughout this chapter. The nucleus of this chapter is focused on exploring the potential PCMs available for the real-time applications as well as on reporting the research studies performed on thermal analysis methods for the PCMs, in recent times. Emphasis is also been laid on the thermal analysis methods on the nanomaterials-based PCMs for the suitable TES applications.

Effective uranium biosorption by macrofungus (Russula sanguinea) from aqueous solution: equilibrium, thermodynamic and kinetic studies

Russula sanguinea (R. sanguninea) macrofungus was employed as a novel cost-effective biosorbent for efficient removal of U(VI) ions from aqueous solution. FT-IR spectroscopy and SEM/EDS technique were used for morphological and chemical characterizations. The maximum adsorption capacity of the macrofungus was found as 174.3xa0mg/g at pH 5 and 20xa0°C. The kinetic data best fit with the pseudo-second-order kinetic model (r2u2009>u20090.99 for the studied temperatures). The exothermic and spontaneous nature of the biosorption process was confirmed by the thermodynamic findings. The reusability test demonstrated that the macrofungus had a good sorption/desorption performance.

Effects of carbon nanotubes additive on thermal conductivity and thermal energy storage properties of a novel composite phase change material

Fatty acids are commonly preferred as phase change materials for passive solar thermoregulation due to their several advantageous latent heat thermal energy storage (LHTES) properties. However, further storage container requirement of fatty acids against leakage problem during heating period and also low thermal conductivity significantly limit their application fields. To overcome these drawbacks of capric acid–stearic acid eutectic mixture as phase change material, it was first impregnated with expanded vermiculite clay by melting/blending method and then doped with carbon nanotubes. The effects of carbon nanotubes additive on the chemical/morphological structures and LHTES properties of the composite phase change material and thermal enhanced change phase change materials were investigated by scanning electron microscope, Fourier transform infrared spectroscopy, X-ray diffraction, differential scanning calorimetry and thermogravimetric analysis analysis techniques. The differential scanning calorimetry results showed that the form-stable composite phase change materials and thermal enhanced composite phase change materials have melting temperatures in the range of 24.35–24.64℃ and latent heat capacities between 76.32 and 73.13u2009J/g. Thermal conductivity of the composite phase change materials was increased as 83.3, 125.0 and 258.3% by carbon nanotubes doping 1, 3 and 5u2009wt%. The heat charging and discharging times of the thermal enhanced -composite phase change materials were reduced appreciably due to the enhanced thermal conductivity without notably influencing their LHTES properties. Furthermore, the thermal cycling test and thermogravimetric analysis findings proved that all fabricated composites had admirable thermal durability, cycling LHTES performance and chemical stability.