Pristine and Se doped ZnO nanoparticles (NPs) were successfully synthesized by thermo-mechanical method and their structural, morphological and optical properties are characterized. Here in, a series of experiments were carried out where cholesterol is treated with same concentration of Pristine as well as Se doped ZnO NPs. Several Cholesterol oxidation products (COP’s) such as 25-hydroxycholesterol and 26-hydroxycholesterol, 7a-hydroxycholesterol, 7ß-hydroxycholesterol, 7-ketocholesterol are formed as observed by HPLC analysis. The batch of 5 wt % Se doped ZnO NPs exhibited highest cholesterol degradation efficiency followed by pristine ZnO NPs and 2 wt % Se doped ZnO NPs. The peak area corresponding to 7-ketocholesterol and 25-hydroxycholesterol is found to be 200980 AU and 200986 AU respectively. The mechanism of cholesterol degradation was correlated with incorporation of oxygen vacancies due to Se doping, which were likely intermediate levels for transiting photoexcited charge carriers for generation of hydroxyl radicals. Further, hydroxyl radicals generated during interaction of ZnO nanoparticles with aqueous media have been determined using terephthallic acid assay and 2', 7'-di-chlorofluorescein (DCF) assay.

Halloysite nanotube/ferrihydrite (HNT/HFO) nanocomposites have been synthesized using a simple chemical precipitation method using only one-pot method. The synthesized nanocomposites were characterized for its physicochemical as well as morphological characteristics through X-Ray Diffraction (XRD), Fourier Transform Infrared (FTIR) Spectroscopy, Transmission Emission Microscopy (TEM), Energy Dispersive X-Ray Spectroscopy (EDX) as well as Brunauer–Emmett–Teller (BET). The morphology of the synthesized nanocomposites revealed the attachment of HFO to the lining of HNT which confirms its successful grafting on HNT. XRD patterns has revealed the nanocomposite having monoclinic structure in which it agrees with the FTIR results. The high surface area of 328.6 m2/g and high aspect ratio of the HNT-HFO nanocomposites has endowed it with enforcing ability and increased its water absorption capability, which in turn making it highly hydrophilic. The high hydrophilicity and adsorption ability of the nanoparticles has open a wide opportunity for it to be utilized in separation of wastewater.

Consistent with the US Environmental Protection Agency, heavy metals are classified as carcinogenic to humans. Their numerous agricultural, industrial, domestic, medical, and technical requirements have resulted in their widespread dissemination in the environment. This article examines a new green adsorbent for the removal of two hazardous heavy metals, lead and mercury. The impact of contact time, pH, initial concentration, and temperature on the adsorption capacity of Pb2+ and Hg2+ were evaluated. Experimental data were analyzed by adsorption models. The equilibrium data were well adapted to the Langmuir adsorption model. The results show that the adsorption is homogeneous and localized in a monolayer. In addition, the maximum adsorption capacity was 277.78 mg/g for Pb2+ and 64.52 mg/g for Hg2+ from Langmuir isotherm. Thermodynamic data, including free energy (?G°), enthalpy (?H°), and entropy (?S°) variations were also considered. The important point is that the negative value of ?G° signifies the spontaneity of the adsorption process of the heavy metals-NiO/ZSM-5 system.

Recently, safety concerns over the handling of nanomaterials have become an important issue. The aim of the present study was to optimize the key parameters in the hydrothermal synthesis of CuInS2 quantum dots (QDs) as a non-toxic alternative to the cadmium-based QDs, that historically had dominated the literature. Response surface methodology (RSM) in combination with D-optimal design was applied to optimize the synthesis and evaluate the PL intensity as the response which described by a reduced quadratic equation. The relationship between the PL intensity and independent variables (ligand/precursor, reaction time, reaction temperature, pH, and precursors ratio) was investigated using reduced quadratic polynomial equations. The produced QDs in the optimum condition were analyzed by UV-Vis, FE-SEM, and FTIR. The results showed that the nanoparticles have a high PL intensity and a red shift in both emission and absorbtion spectra which is a splendid point for their applications specially in bioimaging. The interaction between variables was not significant and the temperature was the most effective variable of PL intensity. A good agreement between predicted model and experimental data confirmed the correlated model.

In this study, we have synthesized a new Fe3O4/AC nanocomposite using low cost adsorbent by microwave assisted in situ co-precipitation technique that was used as an effective adsorbent for the removal of methylene blue (MB) using the Taguchi design method as an optimization strategy. The optimum parameters are pH 7, Fe3O4/AC nanocomposite dose 0.03 g, contact time 30 min, initial concentration of MB 25 mg/L and temperature 298 K. The obtained results of ANOVA show that their percent contribution in descending order is pH (66.81%) > adsorbent dose (25.54%) > temperature (4.83%) > initial MB concentration (1.23%) > contact time (0.32%). The kinetic data were fitted to the pseudo-first-order, pseudo-second-order and intra-particle diffusion models and adsorption of MB dye followed pseudo-second-order kinetic. The obtained values of regression coefficient for Langmuir (0.98), Frendluich (0.93) and Dubinin–Radushkevich (0.94) showed that adsorption process fits to the Langmuir isotherm and the maximum adsorption capacity is 384.6 mg/g. Moreover, the thermodynamics studies suggested the spontaneous nature of adsorption process.

The green synthesis of palladium oxide nanoparticles using Dictyota indica seaweed extract was investigated. Dictyotales is a large order in the brown algae (class Phaeophyceae). The color of the reaction mixture changed which indicated the formation of palladium oxide nanoparticles. UV-Visible, SEM, TEM, XRD, and FTIR analysis determined the characteristics of synthesized nanoparticles. The UV-Visible analysis showed the formation of palladium oxide nanoparticles. SEM and TEM analyses presented the palladium oxide nanoparticles have a spherical shape and based on DLS analysis with the average particle diameter of 19nm. The comparisons of the nanoparticle size with different biological synthesis were studied which revealed this methodology offer smallest size. The crystallographic parameters of the synthesized Pd nanoparticles were as follows: crystalline structure (cubic), space group (Fm-3m), and lattice parameter (a=5.6500, b=5.6500, c=5.6500, a=90, ß=90, and ?=90). FTIR analysis indicated the presence of a palladium oxide group in the product. The removal efficacy of cadmium by the palladium oxide nanoparticles was investigated to optimize the pH, contact time, dose of adsorbent and concentration of cadmium. The results showed that optimum conditions for cadmium removal from water were obtained at pH 8, 500 mg/l adsorbent dose and 20 min contact time, wherein in these circumstances the removal of cadmium was 82.82%. The adsorption isotherms primacy was as follows, Langmuir R2=0.9904> Freundlich R2=0.9857> Temkin R2=0.8791.

In the present work, Graphene Oxide (GO) nano particles with 0.1, 0.2, 0.4 and 0.8 weight percentages (wt.% ), synthesized by Hummer method entered into the Di-Calcium Silicate (C2S) matrix (synthesized with using Pechini method and their nano structural and mechanical characteristics studied by XRD (X-ray diffraction), FTIR (Fourier transform infrared), GPS 132 A, 4- probe techniques and emission factor analyses. To study and examine GO-C2S nano composites as an environmentally- friendly Material for sustainable Development of Cement Structure 4- capacitor form, with Metal (Al) /GO-C2S composite/ Si substrate are fabricated. The quality factor and dissipation factor were measured by GPS 132 A tool. The obtained results show that sample with 0.4% wt. of GO nano particles has 0.625 fraction emission factor and higher quality factor (32.4), measured at two frequencies of 120 KHz and 1 KHz. Therefore C2S/ GO nano composite with 0.4 wt.% GONs can be therefore introduced as a good additive to reduced emission factor for production of cement and dissipation factor.

Given the gradual development of drug resistance in different bacterial species, it is necessary to search for new drugs with effective broad spectrum antimicrobial activity. Therefore, recent studies on various nanometal oxides such as copper oxide and on antibacterial peptides including nisin as antibacterial agents are especially important. The present study aimed to investigate the synergistic effect of nisin-conjugated copper oxide nanoparticles (CuO NPs) on the genome of E. coli selected as a Gram-negative model. After being cultured in a Nutrient Broth medium, the bacteria were treated with CuO NPs at 15, 30, 40, and 60µg/mL, with nisin at 30, 60, 90, and 120µg/mL, and with nisin-conjugated CuO NPs at 10, 20, and 30µg/mL and were then incubated. The optical densities of the samples were read at 600nm and their DNA was extracted. RAPD-PCR was used to study genomic effects, and statistical analysis was performed employing NTSYS-PC based on the DICE coefficient, the similarity matrix, and the drawn dendrogram. Results showed that the combination of CuO NPs and nisin had synergistic effects and was able to inhibit growth more than either of them used alone. However, this combination had no synergistic effects on the genome and caused minimal changes in the DNA sequence.