Nanocrystalline metal ferrites (MFe₂O₄, M = Co, Ni, Cu, Mg, and Zn) were successfully synthesized via autocombustion synthesis using egg white. X-ray diffraction (XRD) measurements revealed the crystallization of the entire ferrites either in the tetragonal structure, such as in the case of CuFe₂O₄, or cubic spinels such as in other studied ferrites. The Fourier transform infrared spectral study revealed the characteristic vibration bands of ferrites. Compared to other synthesis methods, the observed variation in the obtained structural parameters could be due to the different cation distribution of the prepared ferrites. In agreement with XRD measurements, the transmission electron microscopy images showed agglomerated particles with cubic morphology for all ferrites. On the other hand, CuFe₂O₄ showed tetragonal morphology. The magnetization values were found to vary with the type of the metal ion, and CoFe₂O₄ showed the highest one (42.8 emu/g). Generally, the lower magnetization values obtained than those reported in the literature for all studied ferrites could be attributed to the smaller particle sizes or the cation redistribution. The obtained coercivity values are observed to be higher than their related values in the literature, exhibiting the impact of the present synthesis route. Ac-conductivity as a function of temperature and frequency indicated semiconducting properties with the observed change in the conduction mechanism by increasing the temperature. The obtained low dielectric constant values could suggest using the entire ferrites in high-frequency applications such as microwave devices.

Herein, ternary composites from polypyrrole (PPy), Mn_0.8Zn_0.2Fe₂O₄ (MZF), and graphite oxide (GO) were prepared to remove acid red dye (AR1) from wastewater. MZF was synthesized using spent Zn–C batteries, acid leaching, and sucrose auto-combustion processes; GO was prepared via oxidation and exfoliation of graphite. The composites were prepared by adding MZF and GO during the in-situ polymerization of pyrrole. Different PPy/MZF/GO (PMG) composites were prepared by changing the weight ratios of the PPy, MZF, and GO. We investigated the prepared composites’ structural, magnetic, and electrical/dielectric properties. We evaluated different experimental conditions’ influences on dye removal performance, such as pH, dosage, dye concentration, temperature, and contact time. XRD, FT-IR, and magnetic properties indicated that PPy completely coated the other contents. The electrical/dielectric properties improved while increasing the GO ratio. The PMG at GO content 50 wt.% (PMG50) showed the most efficient ratio for better removing AR1 from wastewater.

Passivated-carbon quantum dots (P-CQDs) have been attracting great interest as an antimicrobial therapy tool due to their bright fluorescence, lack of toxicity, eco-friendly nature, simple synthetic schemes, and possession of photocatalytic functions comparable to those present in traditional nanometric semiconductors. Besides synthetic precursors, CQDs can be synthesized from a plethora of natural resources including microcrystalline cellulose (MCC) and nanocrystalline cellulose (NCC). Converting MCC into NCC is performed chemically via the top-down route, while synthesizing CODs from NCC can be performed via the bottom-up route. Due to the good surface charge status with the NCC precursor, we focused in this review on synthesizing CQDs from nanocelluloses (MCC and NCC) since they could become a potential source for fabricating carbon quantum dots that are affected by pyrolysis temperature. There are several P-CQDs synthesized with a wide spectrum of featured properties, namely functionalized carbon quantum dots (F-CQDs) and passivated carbon quantum dots (P-CQDs). There are two different important P-CQDs, namely 2,2′-ethylenedioxy-bis-ethylamine (EDA-CQDs) and 3-ethoxypropylamine (EPA-CQDs), that have achieved desirable results in the antiviral therapy field. Since NoV is the most common dangerous cause of nonbacterial, acute gastroenteritis outbreaks worldwide, this review deals with NoV in detail. The surficial charge status (SCS) of the P-CQDs plays an important role in their interactions with NoVs. The EDA-CQDs were found to be more effective than EPA-CQDs in inhibiting the NoV binding. This difference may be attributed to their SCS as well as the virus surface. EDA-CQDs with surficial terminal amino (-NH₂) groups are positively charged at physiological pH (-NH³⁺), whereas EPA-CQDs with surficial terminal methyl groups (-CH₃) are not charged. Since the NoV particles are negatively charged, they are attracted to the positively charged EDA-CQDs, resulting in enhancing the P-CQDs concentration around the virus particles. The carbon nanotubes (CNTs) were found to be comparable to the P-CQDs in the non-specific binding with NoV capsid proteins, through complementary charges, π-π stacking, and/or hydrophobic interactions.