Browsing by Author "Çam, NF"

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    Styrene-based unsaturated polyester-tungsten(VI) oxide composites: Preparation and investigation of their radiation shielding and thermal properties
    Körpinar, B; Öztürk, BC; Çam, NF; Akat, H
    In this study, the thermal and radiation shielding properties of composites obtained using different ratios of tungsten(VI) oxide unsaturated polyester were investigated. Composites were prepared using WO3.2H(2)O powder in different ratios (10%, 20%, 30%, 40%, and 50%.), and based on Styrene unsaturated polyester were used as resins. The linear attenuation coefficients of the composites were measured by the NaI(Tl) gamma spectrometry system. The attenuation coefficients were also calculated theoretically by the XCOM platform, taking into consideration the basic analysis of composites, and compared with empirical outcomes. According to the results of XRD and particle size distribution of WO3.2H(2)O powder demonstrated had obvious diffraction peaks and its pore size distribution values were good. When the thermal degradation curves of the composites are examined, it is seen that the remaining ash amounts of the prepared composites and the % mass of the prepared composites overlap. It was clear that the best shielding material in the studied composites was styrene-based unsaturated polyester +50% WO3.2H(2)O with a higher linear attenuation coefficient.
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    Novel starch-tungsten (VI) oxide biocomposites: Preparation, characterization, and comparisons between experimental and theoretical photon attenuation coefficients
    Körpinar, B; Öztürk, BC; Çam, NF; Akat, H
    This study synthesized biocomposites containing starch and WO3 at varying ratios of 10 %, 20 %, 30 %, 40 %, and 50 % and assessed their thermal and radiation-shielding properties. These biocomposites were characterized using Fourier-transform infrared spectroscopy, X-ray diffraction (XRD) analysis, particle-size distribution assessments, scanning electron microscopy-energy dispersive X-ray spectroscopy, and thermogravimetric analysis-differential thermogravimetry measurements. Furthermore, the linear attenuation coefficients of the biocomposites were experimentally measured using an NaI(Tl) gamma spectrometry system and theoretically computed using XCOM and GAMOS simulations for comparisons. The XRD and particle-size distribution profiles of the WO3.2H2O powder, respectively, demonstrated evident diffraction peaks and favorable pore-size distributions. Morphological characterizations revealed that the WO3 particles were homogeneously dispersed throughout the starch matrix without any agglomeration. Comparisons of the thermal degradation rates revealed that the pure starch and starch +50%WO3 biocomposite began decomposing at approximately 200 degrees Cand 300 degrees C, respectively, indicating that increasing WO3 proportions enhanced thermal stability. Furthermore, the starch +50%WO3 biocomposite demonstrated the highest experimental linear attenuation coefficient, with a value of 0.2510 +/- 0.0848 cm-1 at a gamma energy of 662 keV. Meanwhile, XCOM and GAMOS simulations revealed theoretical attenuation coefficients of 0.1229 and 0.1213 cm-1 for pure starch and 0.2202 cm-1 and 0.2178 cm-1 for the starch +50%WO3 biocomposite at 662 keV, respectively.