Evaluation of antimicrobial and dyeing properties of walnut (Juglans regia L.) green husk extract for cosmetics

Walnut green husk is one of the main waste products from walnut and could be used as a source of natural dyeing compounds such as juglone. The present study was conducted to evaluate the effective use of walnut green husk extract as a natural hair dye. Dyeing properties, fastness and antimicrobial behaviours of dyed hair and also a skin irritation test for natural hair dye on rat skin were examined. When the extract was mixed with ascorbic acid as a developer, ferrous sulphate as a mordant, and Aloe vera extract used as a secondary mordant and also a cosmetic ingredient, the reaction resulted in a dark‐brown colour on hair samples. The dyed hair exhibited appropriate colour strength having excellent morphology for a hair surface coated with dye molecules. In addition, the dyed hair possessed good resistance to washing and daylight fastness, without any irritant properties as shown in a rat model, although high concentrations of iron‐based mordant may be problematic for long‐term usage. This paper also suggests the use of natural mordants such as lactic and oxalic acids to avoid any probable risks. Walnut green husk extract was an appropriate natural hair dyeing agent in practice and showed maximum antimicrobial activity compared with semi‐synthetic and commercial hair dyes. The results demonstrated that walnut green husk can be used as an economical, valuable, eco‐friendly and safe source of dyeing and antimicrobial agents for cosmetic products.     

The effect of substrate temperature on microstructural evolution and hardenability of tungsten carbide coating in hot filament chemical vapor deposition

Effect of substrate temperature on microstructural evolution and hardenability of tungsten carbide coating produced by hot filament chemical vapor deposition (HFCVD) process was studied. Annealed sheets of 316L stainless steels were used as the substrate. HFCVD technique, with substrate temperatures of 400 and 500°C, was used to deposit tungsten carbide coating on these sheets. Field Emission Scanning Electron Microscope (FE‐SEM) was used to study the evolution of microstructure. X‐Ray Diffraction spectroscopy was used to analyze the phases formed and Raman spectroscopy was employed to differentiate molecular composition of the coatings. The amount of the porosity of the coatings was measured and Vickers hardness measurement was used for hardness assessment. Results show that the tungsten carbide coatings have a honeycomb structure and increasing the temperature of the substrate increases the amount of porosity of the coating. XRD results showed that 3 different crystalline structures containing W, WC, and W₂C were formed in the coating deposited on the 316L stainless steel. Increasing the temperature of the deposition has increased the intensity of the peaks in the XRD results. Raman spectroscopy results indicated the presence of a carbon in the tungsten carbide coatings. Finally, microhardness of the tungsten carbide coating increases with increasing the temperature of the substrate.     

Investigation of the effect of magnetic field on mass transfer parameters of CO2 absorption using Fe3O4‐water nanofluid

In this study, the enhancement of physical absorption of carbon dioxide by Fe₃O₄‐water nanofluid under the influence of AC and DC magnetic fields was investigated. Furthermore, a gas‐liquid mass transfer model for single bubble systems was applied to predict mass transfer parameters. The coated Fe₃O₄ nanoparticles were prepared using co‐percipitation method. The results from characterization indicated that the nanoparticles surfaces were covered with hydroxyl groups and nanoparticles diameter were 10–13 nm. The findings showed that the mass transfer rate and solubility of carbon dioxide in magnetic nanofluid increased with an increase in the magnetic field strength. Results indicated that the enhancement of carbon dioxide solubility and average molar flux gas into liquid phase, particularly in the case of AC magnetic field. Moreover, results demonstrated that mass diffusivity of CO₂ in nanofluid and renewal surface factor increased when the intensity of the field increased and consequently diffusion layer thickness decreased. © 2016 American Institute of Chemical Engineers AIChE J, 63: 2176–2186, 2017     

Synthesis of water dispersible reduced graphene oxide via supramolecular complexation with modified β-cyclodextrin

A noncovalent functionalization of the edges of reduced graphene oxide (RGO) with β-cyclodextrin-graft-hyperbranched polyglycerol (β-CD-g-HPG) was successfully performed via a host-guest interaction. The results showed that β-CD-g-HPG disperses the graphene sheets better than pure β-CD or HPG. The resulted supramolecular structure is stable in neutral water medium more than one week. However, in acidic medium the host-guest interaction is collapsed and graphene nanosheets precipitate.     

Investigating the effect of nano-silica on efficiency of the foam in enhanced oil recovery

Due to the vast production of crude oil and consequent pressure drops through the reservoirs, secondary and tertiary oil recovery processes are highly necessary to recover the trapped oil. Among the different tertiary oil recovery processes, foam injection is one of the most newly proposed methods. In this regard, in the current investigation, foam solution is prepared using formation brine, C₁₉TAB surfactant and air concomitant with nano-silica (SiO₂) as foam stabilizer and mobility controller. The measurements revealed that using the surfactant-nano SiO₂ foam solution not only leads to formation of stable foam, but also can reduce the interfacial tension mostly considered as an effective parameter for higher oil recovery. Finally, the results demonstrate that there is a good chance of reducing the mobility ratio from 1.12 for formation brine and reservoir oil to 0.845 for foam solution prepared by nanoparticles.     

Synthesis of polybutadiene nanoparticles by emulsion polymerization: The effect of electrolyte and initiator type on particle size and reaction kinetics

Emulsion polymerization of the butadiene (Bu) was performed in the presence of disproportionate potassium rosinate (DPR) as anionic emulsifier, potassium hydroxide (KOH), and potassium carbonate (K₂CO₃) as electrolytes, and three different initiators including potassium persulfate (KPS), 2,2^′-azobisisobutyronitrile (AIBN) or 4,4′-azobis(4-cyanovaleric acid) (ACVA, also known as VAZO) at 70 °C. Latexes were prepared with a solid content of about 30 wt%. The particle size and its distribution were measured by dynamic light scattering (DLS) analysis, while the polymerization conversion was determined gravimetrically at different time intervals. Results on the emulsion polymerization of Bu in the presence of KOH and K₂CO₃ co-electrolytes showed that adding KOH to the reaction media decreases the polymerization rate. Positive effect of co-electrolytes on the control over polybutadiene latex (PBL) particles size and its distribution was also confirmed, where K₂CO₃ played roles as electrolyte and pH buffer and KOH served double roles as electrolyte and alkaline supplier of the reaction media. Complete solubility of the AIBN in Bu resulted in higher rate of polymerization in the presence of AIBN in comparison to other initiators, i.e., VAZO or KPS. The results showed that initiator type plays a significant role on the formation of PBL nanoparticles and kinetics of the polymerization. The kinetic studies revealed that emulsion polymerization of Bu follows case 1 (i.e., \(\bar{n}\) ?0.5, where \(\bar{n}\) indicates average number of the propagating chains per particle) of the Smith-Ewart kinetics.     

On physical and antibacterial properties and drug release behavior of poly(vinyl alcohol) hydrogels: effect of drug loaded chitosan nanoparticles

This paper deals with influence of chitosan nanoparticles (CNPs) loaded by tetracycline, as a drug, on the physico-mechanical and antibacterial properties as well as drug release behavior of poly(vinyl alcohol), PVA, hydrogels prepared by electron beam irradiation. The formation of spherical chitosan particles in nanoscale size prepared by an ionic gelation method was confirmed by FTIR and UV spectroscopy, and scanning electron microscopy analyses. The drug release kinetic studies from drug loaded chitosan nanoparticles (DLCNPs) at pH = 7.4 revealed a linear and steady release behavior over long period of time. The theoretical analysis of the swelling kinetic data, using Peppas’s model showed that the swelling kinetic is governed by Fickian diffusion for all the prepared hydrogels, however, the water diffusion coefficient, and therefore, the swelling content were lower for the hydrogels loaded with DLCNPs as compared to the ones with the neat drug. In agreement with these results, the hydrogels containing DLCNPs exhibited a more controlled drug release behavior with significantly stronger antibacterial activity. The tensile mechanical properties of the hydrogels not affected by the DLCNPs were found to be suitable for wound dressing applications.     

Theoretical kinetic study of the reaction between dimethyl disulfide and OH radicals

The potential energy profile of the reaction between dimethyl disulfide and OH^? radicals is explored by utilizing ab initio and hybrid meta density functional theory methods. Having the energies and structural data of the stationary points, statistical rate theories, such as transition state theory and variable reaction coordinate-transition state theory, are employed to compute the overall rate constants, and discuss the mechanism and product channels. On the basis of the calculations, the overall rate coefficient is predicted to be 2.49?×?10^?10?cm³?molecule^?1?s^?1 at 298?K. It is found that in the most favorable pathway, the reaction proceeds via formation of the relatively unstable intermediate CH₃S^?(OH)SCH₃ decomposing rapidly to yield CH₃S^?+CH₃SOH.     

The Ablation and Oxidation Behaviors of SiC Coatings on Graphite Prepared by Slurry Sintering and Pack Cementation

SiC coatings were generated on graphite using slurry sintering (SS) and pack cementation (PC). The samples’ ablation features were assessed by an oxyacetylene torch. The rates of mass ablation of the PC–SiC and SS–SiC coatings were approximated 2.17?×?10^?3 and 9.52?×?10^?3 g s^?1, respectively, decreased by 84.1 and 29.6% compared to the uncoated samples. It was mainly attributed to the formation of a SiO₂ layer on the surface. The continuous SiO₂ molten film formed via the PC–SiC oxidation generates a sealing mechanism which can be an obstacle against the oxygen diffusion and hinder more ablation. This is while discontinuous SiO₂ film formed from the thin SS–SiC cannot protect the graphite effectively. The non-isothermal oxidation test shows that without the SiC coating, the sample weight is lost largely from 25 to 1500 °C, and its weight loss was 2.2% after the TGA. However, after coating, the samples possessed excellent oxidation protection and weight losses of SS–SiC and PC–SiC coatings are down to 1.3 and 0.6%, respectively. The more oxidation of the graphite substrate occurred due to the formation of macrocracks in the coating during the TGA and also the formation of holes on SiO₂ glass layer owing to release of CO or CO₂.     

Ni-TiO2 nanocomposite coating with high resistance to corrosion and wear

Ni-TiO₂ nanocomposite coatings with various contents of TiO₂ nanoparticles were prepared by electrodeposition in a Ni plating bath containing TiO₂ nanoparticles to be codeposited. The influences of the TiO₂ nanoparticle concentration in the plating bath, the current density and the stirring rate on the composition of nanocomposite coatings were investigated. The composition of coatings was studied by using energy dispersive X-ray system (EDX). The wear behavior of the pure Ni and Ni-TiO₂ nanocomposite coatings were evaluated by a pin-on-disc tribometer. The corrosion performance of coatings in 0.5 M NaCl, 1 M NaOH and 1 M HNO₃ as corrosive solutions was investigated by potentiodynamic polarization and electrochemical impedance spectroscopy methods (EIS). The microhardness and wear resistance of the nanocomposite coatings increase with increasing of TiO₂ nanoparticle content in the coating. With increasing of TiO₂ nanoparticle content in the coating, the polarization resistance increases, the corrosion current decreases and the corrosion potential shifts to more positive values.