Experimental study on thermo-physical and rheological properties of stable and green reduced graphene oxide nanofluids: Hydrothermal assisted technique

In this study a dehydration hydrothermal technique has been used to introduce a simple, environmentally friendly and facile method for manufacturing highly dispersed reduced graphene oxide for improving the thermo-physical and rheological properties of heat transfer liquids. The hydrothermal reduction of graphene oxide was verified by various characterizations methods such as UV–visible absorption spectroscopy, Zeta potential, Raman spectroscopy, X-ray photoemission spectroscopy, X-ray diffraction, Fourier transform infrared spectroscopy, and transmission electron microscopy. A thorough investigation was conducted on the thermo-physical properties of reduced graphene oxide at concentrations of 0.02, 0.04, 0.06, and 0.08?wt% under different temperatures. Significant improvements in electrical and thermal conductivity were obtained by adding a small amount of hydrothermal-assisted reduced graphene oxide (h-rGO) in the suspension. The viscosity and density remained relatively unchanged with the increase of concentrations where the pH was maintained within the desirable value, despite the fact that no additive was used during the reduction process. It is noteworthy to highlight that the h-rGO aqueous suspensions have shown Newtonian behavior. Results indicated that the h-rGO could be employed as a promising additive for conventional heat transfer liquids for different thermal applications.     

The therapeutic effect of low-level laser on repair of osteochondral defects in rabbit knee

INTRODUCTION: Low level laser therapy (LLLT) has been shown to enhance collagen production and wound healing but its effect on cartilage repair from biomechanical point of view is not known yet. The aim of present study was to evaluate the biomechanical behaviour of repairing osteochondral defect in rabbits which received a pulsed low-level gallium-arsenide (Ga-As) laser irradiation. MATERIALS AND METHODS: Osteochondral defects with 5mm diameter and 4mm in depth induced by drilling in right femoral patellar grooves of 41 adolescent male rabbits. They were divided into experimental and control groups. Experimental group received pulsed Ga-As (890nm) laser irradiation with energy density of 4.8J/cm(2). The rabbits in control group received placebo LLLT with shut-down equipment. The control defects were allowed to heal spontaneously. Each group were divided into three subgroups: A, B and C. Subgroups A, B and C were sacrificed on 4, 8, and 16 weeks after surgery. The knee joint were removed, and the defects were examined biomechanically by in situ-indentation method. The thickness, instantaneous and equilibrium indentation stiffness was measured during the test. Data were analysed using ANOVA and independent sample t-test. RESULT: While no difference was observed in the repaired cartilage biomechanical properties among 4th, 8th, 16th weeks in study groups. The equilibrium indentation stiffness of experimental group was significantly higher in 8th week in comparison with control group. CONCLUSION: LLLT significantly enhances the stiffness of repairing tissue in the 8th week post injury in osteochondral defects in rabbits.     

The scattering of P-waves by a piezoelectric particle with FGPM interfacial layers in a polymer matrix

Propagation of P-wave in an unbounded elastic polymer medium which contains a set of nested concentric spherical piezoelectric inhomogeneities is formulated. The polymer matrix is made of Epoxy and is isotropic; each phase of the inhomogeneity is made of a different piezoelectric material and is radially polarized and has spherical isotropy. Note that the individual phases are homogeneous, and all interfaces are perfectly bonded. The scattered displacement and electric potentials in the matrix are expressed in terms of spherical wave vector functions and Legendre functions, respectively. The transmitted displacement and electric potentials within each phase of the piezoelectric particle are expressed in terms of Legendre functions. The equations of motion and electrostatics in each phase of the piezoelectric inhomogeneity lead to a system of coupled second order differential equations, which is solved using the generalized Frobenius series. The present theory is extended to the case where the core of the inhomogeneity is made of PZT-4 and its coating is made of functionally graded piezoelectric material (FGPM) whose microstructural composition varies smoothly from PZT-4 at the core–coating interface to Epoxy at the coating–matrix interface. The effects of different types of variation in the electro-mechanical properties of FGPM on scattering cross-section and other electro-mechanical fields are addressed. The present theory is valid for arbitrary coating thickness, and arbitrary frequencies.     

Fischer–Tropsch synthesis using zeolitic imidazolate framework (ZIF-7 and ZIF-8)-supported cobalt catalysts

The Fischer–Tropsch synthesis using cobalt catalysts supported on zeolitic imidazolate frameworks (ZIFs), ZIF-7 and ZIF-8, has been investigated. ZIF-7, ZIF-8 and corresponding cobalt-containing catalysts, after preparation, were characterized using various techniques. Thermogravimetric analysis results show that ZIF-7 and ZIF-8 supports have good thermal stability for the Fischer–Tropsch synthesis reaction, and weaker interaction between cobalt and zinc in the ZIF-7 and ZIF-8 supports results in more cobalt reduction. The catalytic performance was evaluated in Fischer–Tropsch synthesis and compared with that of a cobalt catalyst supported on SBA-15 promoted with zinc. The pore structure of the ZIF supports plays an essential role in product selectivity for the prepared catalysts. The carbon number in hydrocarbon products and olefin selectivity depend on cobalt dispersion and support structure owing to the impacts of site density and carrier skeleton on the speed of diffusion-enhanced olefin re-adsorption reactions.     

Neuropeptidomics: Comparison of parallel reaction monitoring and data‐independent acquisition for the analysis of neuropeptides using high‐resolution mass spectrometry

Targeted peptide quantitation by mass spectrometry is a rapidly emerging field. Traditionally it relied on the development and validation of multiple reaction monitoring assays that could comply with a high level of sensitivity, specificity, accuracy and reproducibility in complex biological samples. However, with the introduction of high‐resolution mass spectrometers, other acquisition modes could provide more comprehensive datasets for identification and quantification but also for in‐depth data mining. The objective of this study was to evaluate two analytical approaches, parallel‐reaction monitoring (PRM) and data‐independent analysis (DIA) using a hybrid Quadrupole–Orbitrap mass spectrometer for the quantification of neuropeptides in animal spinal cord tissues. Mouse spinal cord tissues were harvested, homogenized and neuropeptides extracted using a C₁₈ solid‐phase extraction protocol. Chromatography was achieved using a Thermo Biobasic C₈ 100 × 1 mm (5 μm) column. The initial mobile phase conditions consisted of acetonitrile and water (both containing 0.1% of formic acid) at a ratio of 5:95. An 11 min linear gradient was applied up to a ratio of 50:50 and maintained for 3 min. The flow rate was fixed at 75 μL/min and 2 μL of sample was injected. Mass spectrometry analyses were performed using a Thermo Q Exactive Plus MS using PRM and DIA approaches. Quantitative data using an isotopic dilution and a label‐free strategy were obtained for both methods and statistically compared. Using both approaches, we were able to clearly detect endogenous neuropeptides. However, with DIA, mass spectra alone could not distinguish Leu‐Enk and Met‐Enk. We used a Bland–Altman plot (Difference plot) to analyze the agreement between both approaches and no systematic bias was observed. Further statistical analyses, including variance analysis, showed more variability in DIA compared with PRM mode. Further analyses were performed using a label‐free approach and confirmed an increase of the variance using a DIA approach.     

Thermokinetic characterisation of tin(II) chloride

Thermokinetic behaviour of SnCl₂ was investigated using differential scanning calorimetry and thermogravimetry techniques under non-isothermal conditions in air, complemented by electron microscopy and Raman spectroscopy. According to the results obtained, the oxidation of SnCl₂ at the heating rates of 5 and 100 °C min^?1 leads to the in situ formation of highly crystalline SnO₂ nanostructures in the form of nanoparticles and nanorods, respectively. The oxidation of SnCl₂ was found to be a liquid–solid (LS) phase transition at the heating rates equal or lower than 10 °C min^?1 and a gas–solid phase transition at the heating rates equal or greater than 20 °C min^?1. The activation energy of melting, vaporisation and LS oxidation of SnCl₂ was determined to be 198, 93 and 91 kJ mol^?1, respectively.     

Preparation of iron oxide nanocrystals by surfactant-free or oleic acid-assisted thermal decomposition of a Fe(III) alkoxide

A new non-hydrolytic, alkoxide-based route was developed to synthesize iron oxide nanocrystals. Surfactant-free thermal decomposition of the iron 2-methoxy-ethoxide precursors results in the formation of uniform iron oxide nanocrystals with an average size of 5.6 nm. Transmission electron microscope study shows that the nanocrystals are protected against aggregation by a repulsive surface layer, probably originating from the alkoxy-alkoxide ligands. Addition of oleic acid resulted in monodisperse nanocrystals with an average size of 4 nm. Mössbauer analysis confirmed that the nanocrystals mainly consisted of maghemite. Analysis of the magnetic hysteresis loop measurements and the zero field and field cooled measurements displayed an excellent fit to established theories for single-domain superparamagnetic nanocrystals and the size of the magnetic domains correlated well to the crystallite size obtained from transmission electron microscope.     

Remote detection of similar biological materials using femtosecond filament-induced breakdown spectroscopy

We demonstrated the feasibility of remote detection and differentiation of some very similar agricultural-activity related bioaerosols, namely barley, corn, and wheat grain dusts, through nonlinear fluorescence of fragments induced by the high-intensity inside filaments of femtosecond laser pulses in air. The signals were detected in Lidar configuration with targets located at 4.7 m away from the detection system. All the species showed identical spectra, namely those from molecular C₂ and CN bands, as well as atomic Si, C, Mg, Al, Na, Ca, Mn, Fe, Sr and K lines. These identical spectral bands and lines reveal similar chemical compositions; however, the relative intensities of the spectra are different showing different element abundances from these three bio-targets. The intensity ratios of different elemental lines were used to distinguish these three samples. Good reproducibility was obtained. We expect that this technique could be used at long distance and thus played as a sensor of similar biological hazards for public and defense security. PACS 42.68.Wt; 95.75.Fg