PEG mediated NiMn2O4 nanomaterials as a nano catalyst for peroxidase mimetic activity and photocatalytic degradation.

Artificial peroxidases have garnered a lot of attention owing to their tremendous superiority over their natural counterparts. Here, NiMn2O4 nanoparticles have been successfully prepared through PEG assisted hydrothermal method. The varied PEG concentrations significantly altered the morphology and particle size of the synthesizedmaterials. We demonstrate the improved peroxide-like assay of different NiMn2O4 nanoparticles for the first time. Among them, Ni4 nanoparticles exhibit good peroxidase-like activity by generating the oxidation of chromogenic substrate 3, 3', 5, 5'-tetramethylbenzidine (TMB) in the presence of H2O2 and a blue color charge transfer product with an absorption maximum is positioned at 652 nm. These observations led to the development of a method for assessingH2O2 that can be read visually and photometrically. The Ni4 nanoparticles show enhanced kinetics compared to the natural enzyme horse radish peroxidase (HRP) with a lower Km (0.168 mM) value. Additionally, this Ni4 nanosphere applies as a visible light photocatalyst for the degradation of methylene blue (MB) and rhodamine B (Rh B) dyes under visible-light irradiation. Under optimized conditions, the degradationrates of MB and Rh B are 68 and 80.7 %, respectively, after 210 min, and recyclable efficiency is about 99 % for Rh B photocatalytic degradation in the first test and 98 % for five cycles, and about 98 % for MB photocatalytic degradation in the first test and 97 % for five cycles.

Alginate templated synthesis, characterization and in vitro osteogenic evaluation of strontium-substituted hydroxyapatite.

The objective of this study is to explore the potential role of alginate (Alg) in the crystallization of metal-substituted hydroxyapatite, with application in orthopaedic reconstruction. The alginate at different concentrations (0.5 and 1.0 wt%) facilitated in situ mineralization of hydroxyapatite (HA) and strontium-substituted HA (SHA, 10 and 30 mol%). The incorporation of the biopolymer and dopant induced notable changes in HA, including reduced crystal size from 31.0 to 16.4 nm and increased lattice volume from 577.3 to 598.0 Å3. The superior affinity of alginate for Sr2+ than for Ca2+ resulted in higher residual alginate in Alg/SHA (13.0 to 19.0 %) compared to Alg/HA (7.1 to 8.2 %). This residual alginate influenced composite properties: surface charge decreased from -26.5 to -45.7 mV, microhardness increased from 0.33 to 0.54 GPa, and dissolution increased from 0.17 to 0.39 %. The in vitro studies revealed that strontium substitution as well as the organization and crystallographic aspects of apatite regulated osteoblastic cell survival, proliferation, differentiation, and biomineralization. The findings suggest that an alginate concentration of 0.5 wt% is optimal for the crystallization of SHA with 10 mol% substitution, and its resulting composite possesses the ideal biomechanical properties to imitate native bone.

Effect of pectin on the crystallization of strontium substituted HA for bone reconstruction application.

The biomacropolymers of bone extracellular matrix (ECM) guide the growth of hydroxyapatite (HA) with various ionic substitutions. Pectin, a plant polysaccharide with chemical similarities to ECM, was investigated for its potential to promote the crystallization of strontium-substituted HA (SH). The influence of pectin (0.5 and 1.0 wt%) on the in situ mineralization of SH (10 and 30 mol% calcium substitution with strontium) was studied. The preferential affinity of pectin to strontium over calcium favoured the incorporation of strontium in apatite, decreased crystal size (18.85-26.22 nm) and retained more pectin residues (8-16%). The residual pectin strongly interacted with small SH particles, resulting in high microhardness (0.43-0.85 GPa) and high surface charge (-32.1 to -30.3 mV), while weak interaction with large HA particles resulted in low microhardness (0.15-0.25 GPa) and low surface charge (-35.4 to -34.6 mV). The in vitro cellular study using human osteoblast-like MG-63 cells demonstrated that inorganic size and material crystallinity play a vital role in regulating osteogenesis. The study suggests that the synchronization of low pectin concentration (0.5 wt%) and high strontium substitution in HA (30 mol%) offers the desired microhardness and in vitro osteogenic properties to emulate natural bone.

SonoFenton degradation of an azo dye, Direct Red.

The degradation of a reactive azo dye, Direct Red 81 (DR81), by Fenton process and in conjunction with sonolysis (SonoFenton) was studied. The synergistic effect of Fenton process and sonolysis enhanced the degradation of Direct Red 81 in aqueous solutions and the reaction followed the mechanism of hydroxyl radical (HO) oxidation. The influence of the initial substrate concentration, pH and catalyst loading on the rate of decolorisation were studied. The dye decolorisation followed apparent first order kinetics. The optimum conditions for decolorisation were pH=3.0, [Fe(2+)]=0.2 g/l, [H2O2]=5.1×10(-3) mol/l and ultrasonic frequency=120 kHz, 60 W. These conditions yielded 99% decolorisation of DR81 within 75 min. The sonolytic degradation products of DR81 were identified using Electrospray Ionization-Mass Spectrometry (ESI-MS). The presence of CO3(2-), HCO3(-), Cl(-), NO3(-), and SO4(2-) ions in the dye solution did not have a considerable effect on the decolorisation efficiency. This study demonstrates that Fenton and SonoFenton methods can effectively decolorize DR81 dye in waste water. The dye concentration used in this study is higher compared to earlier studies illustrating the effective mineralization by the SonoFenton process. The mechanism of dye degradation is also proposed.

Surfactant intercalated alpha-hydroxides of cobalt and nickel and their delamination--restacking behavior in organic media.

Dodecyl sulfate and dodecylbenzene sulfonate intercalated alpha-hydroxides of nickel and cobalt were synthesized by ammonia precipitation. These solids delaminate to give a colloidal dispersion of layers in organic solvents such as 1-butanol. The dispersed layers could be reassembled either by evaporation of the colloid or by coagulation by the addition of a polar solvent.