This work is dedicated to the synthesis, characterization, and adsorption performance of reduced graphene oxide-modified spinel cobalt ferrite nanoparticles. The as-synthesized reduced graphene oxide cobalt ferrite (RGCF) nanocomposite has been characterized using FTIR spectroscopy, FESEM coupled with EDXS, XRD, HRTEM, zeta potential, and vibrating sample magnetometer (VSM) measurements. FESEM proves the particle size in the range of 10 nm. FESEM, EDX, TEM, FTIR, and XPS analyses provide the proof of successful incorporation of rGO sheets with cobalt ferrite nanoparticles. The crystallinity and spinel phase of cobalt ferrite nanoparticles have been shown by XRD results. The saturation magnetization (M _s) was measured as 23.62 emu/g, proving the superparamagnetic behavior of RGCF. The adsorption abilities of the synthesized nanocomposite have been tested using cationic crystal violet (CV) and brilliant green (BG) and anionic methyl orange (MO) and Congo red (CR) dyes. The adsorption trend for MO, CR, BG, and As(V) follows RGCF > rGO > CF at neutral pH. Adsorption studies have been accomplished by optimizing parameters like pH (2-8), adsorbent dose (1-3 mg/25 mL), initial concentration (10-200 mg/L), and contact time at constant room temperature (RT). To further investigate the sorption behavior, isotherm, kinetics, and thermodynamic studies have been conducted. Langmuir isotherm and pseudo-second-order kinetic models suited better for the adsorption of dyes and heavy metals. The maximum adsorption capacities (q _m) obtained have been found as 1666.7, 1000, 416.6, and 222.2 mg/g for MO, CR, BG, and As, respectively, with operational parameters such as T = 298.15 K; RGCF dose: 1 mg for MO and 1.5 mg each for CR, BG, and As. Thus, the RGCF nanocomposite was found to be an excellent adsorbent for the removal of dyes and heavy metals.

Structural disorder induced by cryogenic milling and by heating to the amorphous phase in the active pharmaceutical ingredient Griseofulvin has been studied using Raman spectroscopy, X-ray powder diffraction (XRPD), and fluorescence spectroscopy. A broad, exciting-frequency-independent scattering background in the Raman spectra and changes in intensities and splitting of some of the Raman lines due to lattice and molecular modes have been observed. In the cryomilled samples this strong background is deconvoluted into two components: one due to lattice disorder induced by cryomilling and the other due to Mie scattering from nanosized crystallites. A single-component background scattering attributed to lattice disorder is seen in the Raman spectrum of the amorphous sample. Fluorescence measurements showed an intrinsic fluorescence signal in as-received Griseofulvin that does not correspond to the inelastic background in the Raman spectra and, moreover, decreases in intensity upon cryomilling, thus excluding an assignment of the Raman background intensity to impurity- or molecular-defect-induced fluorescence. Wide-angle XRPD measurements on cryomilled Griseofulvin shows a broad two-component background consistent with the background-scattering component in the Raman data associated with lattice disorder, but at longer correlation lengths. Persistence of this disorder to even longer lengths is evident in small-angle synchrotron XRPD data on micronized Griseofulvin taken as a function of temperature from the crystalline to the amorphous phase.

A unique nanoheterostructure, a boron-filled hybrid carbon nanotube (BHCNT), has been synthesized using a one-step chemical vapor deposition process. The BHCNTs can be considered to be a novel form of boron carbide consisting of boron doped, distorted multiwalled carbon nanotubes (MWCNTs) encapsulating boron nanowires. These MWCNTs were found to be insulating in spite of their graphitic layered outer structures. While conventional MWCNTs have great axial strength, they have weak radial compressive strength and do not bond well to one another or to other materials. In contrast, BHCNTs are shown to be up to 31% stiffer and 233% stronger than conventional MWCNTs in radial compression and have excellent mechanical properties at elevated temperatures. The corrugated surface of BHCNTs enables them to bond easily to themselves and other materials, in contrast to carbon nanotubes (CNTs). BHCNTs can, therefore, be used to make nanocomposites, nanopaper sheets and bundles that are stronger than those made with CNTs.

This study evaluates the preparation of novel ternary functional adsorbents based on polyaniline, zinc oxide nanoparticles, and moringa oleifera gum to produce zinc oxide/Moringa oleifera gum-grafted L-methionine-functionalized polyaniline bionanocomposites (ZM-g-Pani) and employed to sequestrate divalent metal ions (Cd²⁺, Hg²⁺ and Pb²⁺) from wastewater samples. The morphological and structural properties of ZM-g-Pani were exploited using FT-IR, FE-SEM/EDS, TEM, and XRD. FT-IR and FE-SEM studies show that the as prepared nanocomposite has an abundant number of reactive groups and a porous structure, thus demonstrating outstanding divalent metal cation removal. FT-IR study confirms that the attachment of L-methionine to polyaniline is facilitated by the C-S linkage. Both TEM and FE-SEM techniques confirmed the clustered granules of ZnO over the surface of polyaniline, which ultimately provided more surface area to adsorb metal ions. The study demonstrated that Cd²⁺, Hg²⁺ and Pb²⁺ ions could undergo physical sorption and chemisorption simultaneously during the adsorption process. The maximum adsorption capacity was 840.33, 497.51, and 497.51 mg/g for Cd²⁺, Hg²⁺, and Pb²⁺, respectively. The impact of co-existing ions, including NO₃⁻, PO₄³⁻, SO₄²⁻, Cl⁻, Na⁺, Cu²⁺, and Al³⁺, showed that there were no notable alterations in the adsorption of the selected metal ions with ZM-g-Pani. ZM-g-Pani showed eight successive regeneration cycles for Cd²⁺, Hg²⁺, and Pb²⁺ with more than 85% removal efficiency.