Search

Water is a critical resource necessary for life to be sustained, and its availability should be secured, appropriated, and easily obtainable. The continual detection of endocrine-disrupting chemicals (EDCs) (ng/L or µg/L) in water and wastewater has attracted critical concerns among the regulatory authorities and general public, due to its associated public health, ecological risks, and a threat to global water quality. Presently, there is a lack of stringent discharge standards regulating the emerging multiclass contaminants to obviate its possible undesirable impacts. The conventional treatment processes have reportedly ineffectual in eliminating the persistent EDCs pollutants, necessitating the researchers to develop alternative treatment methods. Occurrences of the EDCs and the attributed effects on humans and the environment are adequately reviewed. It indicated that comprehensive information on the recent advances in the rejection of EDCs via a novel membrane and membrane bioreactor (MBR) treatment techniques are still lacking. This paper critically studies and reports on recent advances in the membrane and MBR treatment methods for removing EDCs, fouling challenges, and its mitigation strategies. The removal mechanisms and the operating factors influencing the EDCs remediation were also examined. Membranes and MBR approaches have proven successful and viable to eliminate various EDCs contaminants.

In this research work, an attempt of regulating the pH as a sol-gel modification parameter during preparation of SrFe12O19 nanoparticles sintered at a low sintering temperature of 900°C has been presented. The relationship of varying pH (pH 1–14) on structural microstructures and magnetic behaviors of SrFe12O19 nanoparticles was characterized by X-ray diffraction (XRD), field emission scanning microscope (FESEM), thermogravimetric analysis (TGA), Fourier-transform infrared (FTIR), and vibrating-sample magnetometer (VSM). The single-phase SrFe2O19 with optimum magnetic properties can be obtained at pH 1 with a sintering temperature of 900°C. As pH values increase, the presence of impurity Fe2O3 was observed. TGA data-varying pH shows that the total weight loss of most samples was at 30.44% which corresponds to the decomposition process. The IR spectra showed three main absorption bands in the range of 400–600 cm−1 corresponding to strontium hexaferrite. SEM micrographs exhibit a circular crystal type of strontium ferrite with an average crystal size in the range of 53–133 nm. A higher saturation magnetization Ms, remanent magnetization Mr, and hysteresis Hc were recorded to have a large loop of 55.094 emu/g, 33.995 emu/g, and 5357.6 Oe, respectively, at pH 11, which make the synthesized materials useful for high-density recording media and permanent magnets.

Steel waste product had been used as the main source of raw material in the preparation of permanent magnets ferrites. Steel waste product is an impure material that contains the iron oxide and impurities. The steel waste product is a form of flakes is grinding for several hours to form a fine powder. The iron oxide powder is separated from magnetic and non-magnetic particle using magnetic particle separation. The magnetic particle was again been purified by using the Curie temperature separation technique. The magnetic powder was carried out from the purification and oxidize at 500 °C for 6 hours at 2 °C/ mins to form the hematite, Fe2O3, used as a raw powder to prepare SrFe12O19. Microstructure of Nd-doped strontium ferrites, Sr1-xNdxFe12O19, with x = 0.0, 0.1, 0.2, 0.3, 0.4 and 0.5, were prepared through a mechanical alloying technique. Several characterizations have been done, such as X-ray Diffraction (XRD) and Field emission scanning electron microscopy (FESEM). The magnetic properties of coercivity (Hc) and the energy product BHmax of samples are carried out. The magnetic properties of samples were investigated with an expectation of enhancing the magnetic properties by substitutions of Nd3+ ions on Fe3+ ion basis sites. The saturation magnetization Ms revealed magnetic behavior with respect to Nd3+ doping concentration, showing a decrease. The coercivity Hc increased with increasing Nd3+ doping concentration.

The doping mechanism of neodymium ion on barium titanate could be promising a new material for applications in miniature microwave technology and mobile communication systems. Microstructural of Ba6-3xNd8+2xTi18O54, with x=0.15 ceramics at different sintering temperatures were investigated. The samples were prepared by the magnetic stirring method and sintered at a temperature range from 600°C to 1300°C. Sintering effects on the crystallite structure and surface morphology were studied and characterized by XRD and FESEM. The transformation of majority of the phase in the system from barium titanate to barium neodymium titanate was confirmed by XRD pattern due to change in sintering temperature. The change in sample densities was determined using Archimede’s method. Two activation energies of grain growth were observed by using estimated diffusion process. The activation energies were 0.0698 and 0.3348 eV for low sintering and high sintering temperatures respectively.

27Al magic angle spinning (MAS) NMR has been used at two fields (8.45 T and 14.1 T) to follow the optimisation of a sol-gel process to produce yttrium aluminium garnet, Y3Al5O12 (YAG), at moderate temperatures. 27Al MAS NMR is shown to be a highly sensitive tool to determine the presence of the impurity phase, yttrium aluminium perovskite, YAlO3. Single phase, polycrystalline YAG has been successfully synthesized, using this modified sol-gel process, at temperatures as low as 800°C. Chemical shifts, quadrupolar coupling constants and asymmetry parameters are reported for the tetrahedral and octahedral aluminium sites of YAG .