This study investigated the production of Cu²⁺-doped CoFe₂O₄ nanoparticles (CFO NPs) using a facile sol−gel technique. The impact of Cu²⁺ doping on the lattice parameters, morphology, optical properties, and electrical properties of CFO NPs was investigated for applications in electrical devices. The XRD analysis revealed the formation of spinel-phased crystalline structures of the specimens with no impurity phases. The average grain size, lattice constant, cell volume, and porosity were measured in the range of 4.55–7.07 nm, 8.1770–8.1097 Å, 546.7414–533.3525 ų, and 8.77–6.93%, respectively. The SEM analysis revealed a change in morphology of the specimens with a rise in Cu²⁺ content. The particles started gaining a defined shape and size with a rise in Cu²⁺ doping. The Cu_0.12Co_0.88Fe₂O₄ NPs revealed clear grain boundaries with the least agglomeration. The energy band gap declined from 3.98 eV to 3.21 eV with a shift in Cu²⁺ concentration from 0.4 to 0.12. The electrical studies showed that doping a trace amount of Cu²⁺ improved the electrical properties of the CFO NPs without producing any structural distortions. The conductivity of the Cu²⁺-doped CFO NPs increased from 6.66 × 10⁻¹⁰ to 5.26 × 10⁻⁶ ℧ cm⁻¹ with a rise in Cu²⁺ concentration. The improved structural and electrical characteristics of the prepared Cu²⁺-doped CFO NPs made them a suitable candidate for electrical devices, diodes, and sensor technology applications.

This study investigated a ternary CdS/TiO₂/g-C₃N₄ heterojunction for degrading synthetic dyes and hydrogen production from aqueous media through visible light-initiated photocatalytic reactions. CdS, TiO₂, and g-C₃N₄ were combined in different mass ratios through a simple hydrothermal method to create CdS/TiO₂/g-C₃N₄ composite photocatalysts. The prepared heterojunction catalysts were investigated by using FTIR, XRD, EDX, SEM, and UV-visible spectroscopy analysis for their crystal structures, functional groups, elemental composition, microtopography, and optical properties. The rhodamine B dye was then degraded by using fully characterized photocatalysts. The maximum dye degradation efficiency of 99.4% was noted in these experiments. The evolution rate of hydrogen from the aqueous solution with the CdS/TiO₂/g-C₃N₄ photocatalyst remained 2910 μmol·h^-1·g^-1, which is considerably higher than those of g-C₃N₄, CdS, CdS/g-C₃N₄, and g-C₃N₄/TiO₂-catalyzed reactions. This study also proposes a photocatalytic activity mechanism for the tested ternary CdS/TiO₂/g-C₃N₄ heterojunctions.

This study performed in-situ microwave pyrolysis of plastic waste into hydrogen, liquid fuel and carbon nanotubes in the presence of Zeolite Socony Mobil ZSM-5 catalyst. In the presented microwave pyrolysis of plastics, activated carbon was used as a heat susceptor. The microwave power of 1 kW was employed to decompose high-density polyethylene (HDPE) and polypropylene (PP) wastes at moderate temperatures of 400–450 °C. The effect of plastic composition, catalyst loading and plastic type on liquid, gas and solid carbon products was quantified. This in-situ CMP reaction resulted in heavy hydrocarbons, hydrogen gas and carbon nanotubes as a solid residue. A relatively better hydrogen yield of 129.6 mmol/g as a green fuel was possible in this process. FTIR and gas chromatography analysis revealed that liquid product consisted of C₁₃₊ fraction hydrocarbons, such as alkanes, alkanes, and aromatics. TEM micrographs showed tubular-like structural morphology of the solid residue, which was identified as carbon nanotubes (CNTs) during X-ray diffraction analysis. The outer diameter of CNTs ranged from 30 to 93 nm from HDPE, 25–93 nm from PP and 30–54 nm for HDPE-PP mixure. The presented CMP process took just 2–4 min to completely pyrolyze the plastic feedstock into valuable products, leaving no polymeric residue.

Spinel ferrites are widely investigated for their widespread applications in high-frequency and energy storage devices. This work focuses on enhancing the magnetic and dielectric properties of Ni_0.25Cu_0.25Zn_0.50 ferrite series through non-thermal microwave plasma exposure under low-pressure conditions. A series of Ni_0.25Cu_0.25Zn_0.50 ferrites was produced using a facile sol–gel auto-ignition approach. The post-synthesis plasma treatment was given in a low-pressure chamber by sustaining oxygen plasma with a microwave source. The structural formation of control and plasma-modified ferrites was investigated through X-ray diffraction analysis, which confirmed the formation of the fcc cubical structure of all samples. The plasma treatment did not affect crystallize size but significantly altered the surface porosity. The surface porosity increased after plasma treatment and average crystallite size was measured as about ~49.13 nm. Morphological studies confirmed changes in surface morphology and reduction in particle size on plasma exposure. The saturation magnetization of plasma-exposed ferrites was roughly 65% higher than the control. The saturation magnetization, remnant magnetization, and coercivity of plasma-exposed ferrites were calculated as 74.46 emu/g, 26.35 emu/g, and 1040 Oe, respectively. Dielectric characteristics revealed a better response of plasma-exposed ferrites to electromagnetic waves than control. These findings suggest that the plasma-exposed ferrites are good candidates for constructing high-frequency devices.

This study is focused on the kinetics and adsorption isotherms of amine-functionalized magnesium ferrite (MgFe₂O₄) for treating the heavy metals in wastewater. A sol-gel route was adopted to produce MgFe₂O₄ nanoparticles. The surfaces of the MgFe₂O₄ nanoparticles were functionalized using primary amine (ethanolamine). The surface morphology, phase formation, and functionality of the MgFe₂O₄ nano-adsorbents were studied using the SEM, UV-visible, FTIR, and TGA techniques. The characterized nanoparticles were tested on their ability to adsorb the Pb²⁺, Cu²⁺, and Zn²⁺ ions from the wastewater. The kinetic parameters and adsorption isotherms for the adsorption of the metal ions by the amine-functionalized MgFe₂O₄ were obtained using the pseudo-first-order, pseudo-second-order, Langmuir, and Freundlich models. The pseudo-second order and Langmuir models best described the adsorption kinetics and isotherms, implying strong chemisorption via the formation of coordinative bonds between the amine groups and metal ions. The Langmuir equation revealed the highest adsorption capacity of 0.7 mmol/g for the amine-functionalized MgFe₂O₄ nano-adsorbents. The adsorption capacity of the nanoadsorbent also changed with the calcination temperature. The MgFe₂O₄ sample, calcined at 500 °C, removed the most of the Pb²⁺ (73%), Cu²⁺ (59%), and Zn²⁺ (62%) ions from the water.

Carbon dioxide is one of the major greenhouse gases and a leading source of global warming. Several adsorbent materials are being tested for removal of carbon dioxide (CO₂) from the atmosphere. The use of multiwalled carbon nanotubes (MWCNTs) as a CO₂ adsorbent material is a relatively new research avenue. In this study, Fe₂O₃/Al₂O₃ composite catalyst was used to synthesize MWCNTs by cracking ethylene gas molecules in a fluidized bed chemical vapor deposition (CVD) chamber. These nanotubes were treated with H₂SO₄/HNO₃ solution and functionalized with 3-aminopropyl-triethoxysilane (APTS). Chemical modification of nanotubes removed the endcaps and introduced some functional groups along the sidewalls at defected sites. The functionalization of nanotubes with amine introduced carboxylic groups on the tube surface. These functional groups significantly enhance the surface wettability, hydrophilicity and CO₂ adsorption capacity of MWCNTs. The CO₂ adsorption capacity of as-grown and amine-functionalized CNTs was computed by generating their breakthrough curves. BELSORP-mini equipment was used to generate CO₂ breakthrough curves. The oxidation and functionalization of MWCNTs revealed significant improvement in their adsorption capacity. The highest CO₂ adsorption of 129 cm³/g was achieved with amine-functionalized MWCNTs among all the tested samples.