Chitosan (CS) with excellent biomedical properties was mixed with polyvinyl alcohol (PVA) to be used as the spinning solution. The spinning solutions with various concentrations of CS:PVA from 10:90% to 50:50% (v/v) were investigated. Tween 80 (T80) was added in the spinning solutions of CS and PVA. The nanofiber mats with and without T80 addition obtained from the spinning solutions by electrospinning technique were investigated and addressed. The results showed that the viscosity of the CS and PVA spinning solutions increased with increasing the CS concentration, whereas the viscosity decreased after T80 addition. The nanofiber mats with 10–30% CS concentrations were prepared successfully as a smooth surface and high dense nanofiber mat. The average diameter of the nanofiber decreased with increasing the CS concentration. The increase in the CS concentration of the nanofiber mat can increase the mechanical and antibacterial properties, whereas the wettability and drug release property were decreased. Moreover, the nanofiber mats with T80 addition had higher mechanical property and wettability than the nanofiber mats without T80 addition. Finally, the T80 addition can enhance hydrophilicity and promote the drug release property of the nanofiber mat.

The aim of this work was to compare characteristics of hydroxyapatite synthesized by precipitation and ball milling techniques. The cuttlefish bone powder was a precursor in calcium source and the di ammonium hydrogen orthophosphate powders was a precursor in phosphate source. The hydroxyapatite was synthesized by the both techniques such as precipitation and ball milling techniques. The phase formation, chemical structure and morphology of the both hydroxyapatite powders have been examined by X-ray diffractometer (XRD), Fourier transform infrared spectroscope (FTIR) and field emission scanning electron microscope (FESEM), respectively. The results show that the hydroxyapatite synthesized by precipitation technique formed hydroxyapatite phase slower than the hydroxyapatite synthesized by ball milling technique. The FTIR results show the chemical structures of sample in both techniques are similar. The morphology of the hydroxyapatite from the both techniques were sphere like shapes and particle size was about in nano scale. The average particle size of the hydroxyapatite by ball milling technique was less than those synthesized by precipitation technique. This experiment indicated that the ball milling technique take time less than the precipitation technique in hydroxyapatite synthesis.

Fe and Cu powders were mixed at a 50:50 ratio. Then, Fe-Cu alloys were prepared using the ball milling technique with different milling times of 6, 12, 18, 24, 30, 36, and 42 h. The crystalline structure was analyzed using X-ray diffraction (XRD), and it was found that the optimum milling time was 30 h. The homogeneity of the Fe and Cu elements in the Fe–Cu alloys was analyzed using the scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM–EDX) mapping technique. Additionally, the crystal orientation of the Fe–Cu alloys was investigated using transmission electron microscopy (TEM). To fabricate the cathode for nitrate removal via electrolysis, an Fe–Cu alloy milled for 30 h was deposited onto a copper substrate using mechanical milling, then annealed at 800 °C. A pulsed DC electrolysis method was developed to test the nitrate removal efficiency of the Fe–Cu-coated cathode. The anode used was an Al sheet. The synthesized wastewater was prepared from KNO₃. Nitrate removal experiments from the synthesized wastewater were performed for durations of 0–4 h. The results show that the nitrate removal efficiency at 4 h was 96.90% compared to 74.40% with the Cu cathode.

The purpose of this study was to evaluate the radionuclide concentrations of London blue topaz after fast neutron irradiation. The London blue topaz was obtained from Sri Lanka which classified into dark and light colors in the shape of an oval and rectangle with small, medium and large size. The optical property and radionuclide concentrations of London blue topaz have been examine by UV-Visible spectroscopy and HPGe gamma ray spectrometry, respectively. The UV-absorption spectra of topaz was taken in the range of 300 to 800 nm at room temperature. The results showed that the absorption peak of topaz was observed with only broad peaks in the range of 550 to 700 nm and 630 nm that correlated to the O - center in hydroxyl sites which substitutes for fluorine in topaz structure. The radioactivity of dark and light colors in the shape of an oval and rectangle London blue topaz was in the range of 1.437 ± 0.014 to 21.551 ± 0.037 nCi/g (oval dark), 2.958 ± 0.031 to 6.748 ± 0.054 nCi/g (oval light) and 2.350 ± 0.014 to 43.952 ± 0.088 nCi/g (rectangle dark), 1.442 ± 0.023 to 6.748 ± 0.054 nCi/g (rectangle light), respectively. The decay rates of ⁴⁶Sc, ¹⁸²Ta and ⁵⁴Mn isotopes created by irradiation showed that the decay time of the radioactive element depended on the size of the topaz so increased with decreasing the size of topaz. Moreover, the size of topaz also affect the absorption coefficient. This study is applied to predict time of residue dose of topaz for enhancement colorless topaz by neutron radiation treatment.