Modified guar gum: An alternative source for printing of cotton fabric with reactive dye

The alginate thickener is the thickener frequently used for reactive printing of textile. The thickener responds with reactive pigments and thus does not lead to the fabric composition becoming stiffer. In this study, we prepared oxidised natural guar gum with hydrogen peroxide, sodium hypochlorite and sodium hydroxide. All other polysaccharides comprise reactive hydroxyl units with a stronger reactivity that must be replaced if they are to be used in reactive printing. Guar derivatives were synthesised and verified using Fourier-transform infrared (FTIR) spectroscopy. Natural thickeners, synthetic guar gum derivatives, have been employed in textile printing technique. In comparison to other synthetic thickeners, modified environmental guar gum polymer has been shown to be an ecologically friendly and low-cost thickener. Cotton fabric printed with modified guar thickening with hydrogen peroxide has even stronger colour strength than fabric printed with sodium alginate thickener, which is highly favourable. Penetration properties, colour value, colour strength, colour fastness to washing, light and rubbing was compared with alginate thickener (readily available on the market). Guar gum thickeners showed enhanced features versus sodium alginate for reactive printing. Partially replaced guar gum is an appropriate option due to the colour and physical properties.     

The effect of Ti and Si on the mechanical and electrochemical behaviors of the AlCrN coating deposited by CAPVD on 304SS

This study aimed to investigate the effect of adding titanium (Ti) and silicon (Si) elements on the mechanical and electrochemical properties of the AlCrN-based coating. For this purpose, a cathodic arc physical vapor deposition machine was used. Scanning electron microscopy, X-ray diffraction, and nanoindentation tests were utilized for morphological, microstructural, and mechanical characterization of the coatings. The hardness value and plastic deformation index of CrAlN-based coating increase with the presence of Si element. The mechanical properties improvement is attributed to the reduction of crystallite size as well as to the tendency of the coating structure to become amorphous. The specimens were subjected to 3.5 wt% NaCl solution to electrochemical impedance corrosion and potentiodynamic polarization tests. The results showed that by increasing the coatings’ titanium content, the coatings’ corrosion resistance improved. Moreover, by adding 3% and 5% of Si elements to the coatings’ composition, the corrosion resistance of the AlCrTiSiN coatings was enhanced by 35% and 78%, respectively. Improving the corrosion resistance of the AlCrN-based coatings by adding the Si element is attributed to the change in the microstructure and reduction in the porosity of the coatings.     

Computational Simulation for Transport of Priority Organic Pollutants through Nanoporous Membranes

Modeling and simulation of membrane‐based solvent extraction is conducted by computational fluid dynamics (CFD). The process is used for removal of priority organic pollutants from aqueous waste streams in nanoporous membranes. The pollutants include phenol, nitrobenzene, and acrylonitrile extracted by organic solvents. The mathematical model commonly applied to predict the performance of membrane‐based solvent extraction is the conventional resistance‐in‐series model. Here, a comprehensive mathematical model is developed to predict the transport of pollutants through nanoporous media. In order to predict the performance of the separation process, conservation equations for pollutants in the membrane module are derived and solved numerically. The model is then validated through comparing with experimental data reported in the literature. The simulation results were in good agreement with the experimental data for different values of feed flow rates.     

Hydrodynamics and mass transfer study of aliphatic alcohols in airlift reactors

Gas holdup and gas–liquid mass transfer coefficient were considered in an external airlift reactor. Air was sparged through some aliphatic alcohols (methanol, ethanol, n-propanol, and n-butanol) with different concentrations (0–1%, v/v). It was observed that gas holdup and mass transfer coefficient increased with increasing the number of carbons in alcohols. Furthermore, an increment in alcohols concentration increased gas holdup and mass transfer coefficient. The same behavior was observed in external and internal loop airlift reactors although gas holdup and mass transfer coefficient values were less than those of internal airlift reactor. According to the experiments, two correlations for gas holdup and mass transfer were developed.     

Chemistry of Substituted Quinolinones IV. Regioselective Nucleophilic Substitution of 1,3-Dichlorobenzo[f]quinoline

1,3-Dichlorobenzo[f]quinoline 2 was obtained from 1-hydroxybenzo[f]quinolin-3-one 1. Nucleophilic substitution, hydrolysis, hydrazinolysis and azidation reactions of compound 2 have been studied and found regioselective. Also, 1-aminobenzo[f]quinolinone 11 was obtained and used to prepare the benzoquinolinylthiourea derivative 12, naphthonaphthyridinedione 13, benzoquinolinylhydrazonoquinoline 15 and benzo[f]-quinolinyl enamine 17.     

Comparison of microstructure and mechanical properties of plasma-sprayed nanostructured and conventional yttria stabilized zirconia thermal barrier coatings

The main goal of this paper was to evaluate and compare the microstructure and mechanical properties of plasma-sprayed nanostructured and conventional yttria stabilized zirconia (YSZ) thermal barrier coatings (TBCs). To this end, NiCrAlY bond coat, nanostructured, and conventional YSZ coatings were deposited on Inconel 738LC substrate by atmospheric plasma spraying (APS). The mechanical properties of the coating were evaluated using nanoindentation and bonding strength tests. The microstructure and phase composition of the coating were characterized by field emission scanning electron microscopy (FESEM) and X-ray diffractometry (XRD). The nanostructured YSZ coating contained both nanosized particles retained from the powder and microcolumnar grains formed through the resolidification of the molten part of the powder, whereas the microstructure of the conventional YSZ coating consisted of columnar grain splats only. The phase composition of the as-sprayed nanostructured coating consisted of the non-transformable tetragonal phase, while the conventional coating showed the presence of both the monoclinic and non-transformable tetragonal phases. The results of nanoindentation and bonding strength tests indicated that the mechanical properties of the nanostructured coating were better than those of the conventional coating.     

Bubble columns for condensation at high concentrations of noncondensable gas: Heat‐transfer model and experiments

Carrier gas based thermodynamic cycles are common in water desalination applications. These cycles often require condensation of water vapor out of the carrier gas stream. As the carrier gas is most likely a noncondensable gas present in very high concentrations (60–95%), a large additional resistance to heat transfer is present. It is proposed to reduce the aforementioned thermal resistance by condensing the vapor–gas mixture in a column of cold liquid rather than on a cold surface using a bubble column heat exchanger. A theoretical predictive model for estimating the heat‐transfer rates and new experimental data to validate this model are described. The model is purely physics based without the need for any adjustable parameters, and it is shown to predict heat rates within 0 to ?20% of the experimental values. The experiments demonstrate that heat‐transfer rates in the proposed device are up to an order magnitude higher than those achieved in existing state‐of‐the‐art dehumidifiers. © 2012 American Institute of Chemical Engineers AIChE J, 59: 1780–1790, 2013     

Chemical Synthesis and Characterization of Novel Antibacterial Polycyclic Polymer

Polyaniline (PAn) and poly(alkyl substituted anilines) were synthesized in aqueous media by chemical polymerization of alkyl substituted aniline in presence of ammonium peroxydisulphate as an oxidant. The products were investigated in terms of morphology, chemical structure, and mechanism of polymerization with scanning electron microscope (SEM), transmission electron microscopy (TEM), fourier transform infrared (FTIR), and UV–visible spectroscopy (UV–vis), respectively. Results indicated that physicochemical properties of poly(alkyl substituted anilines) depend on substituent groups bonded to N-position. In general, alkyl-substituted PAn have similar chemical and optical properties to parent PAn and it seems that the substituted PAn follow the same polymerization mechanism as reported for PAn. The prepared polymers were then tested for the antibacterial properties against Gram-negative bacteria: Escherichia coli (E. coli). The antibacterial properties were assessed by measuring the zones of inhibition. The antimicrobial results showed clearly that PAn and poly(alkyl substituted anilines) exhibited excellent antibacterial activity against the growth of E. coli microorganism.     

Synthesis,Characterization and Catalytic Activities of Palladium(II) Nitroaryl Complexes

Two palladium(II) nitroaryl complexes trans-[bromo(p-nitrophenyl)bis(triphenylphosphine)palladium(II)] 1 and trans-[bromo(2,4-dinitrophenyl)bis(triphenylphosphine)palladium(II)] 2 have been synthesized. The complexes were characterized by FTIR and NMR (¹H, ¹³C and ³¹P) spectroscopy and elemental analysis. The molecular structure of complex 2, as confirmed by X-ray crystallography, reveals that the Pd atom and its neighboring groups (two PPh₃, Br and phenylene group) lie in a slightly distorted square plane. In the UV–Vis spectra of the complexes 1 and 2, the palladium to aryl charge transfer bands were observed. The emission peaks from the singlet excited states (S₁ → S₀) were observed in the photoluminescence spectra of the complexes. The thermal stability of the complexes has been studied by thermal gravimetric analysis (TGA). TGA data showed that both complexes are thermally stable up to 200 °C, and complex 1 is more stable than 2. The catalytic efficiency of the new palladium(II) complexes was studied as demonstrated using the Sonogashira coupling reactions with good yields. The experimental results suggest that the Sonogashira coupling reactions can be performed at moderate temperature (50 °C) using these new palladium(II) complexes as catalysts.     

Future directions in physiochemical modeling of the thermodynamics of polyelectrolyte coacervates

We review theories of polyelectrolyte (PE) coacervation, which is the spontaneous association of oppositely charged units of PEs and phase separation into a polymer-dense phase in aqueous solution. The simplest theories can be divided into “physics-based” and “chemistry-based” approaches. In the former, PEs are treated as charged, long-chain, molecules, defined by charge level, chain length, and chain flexibility, but otherwise lacking chemical identity, with electrostatic interactions driving coacervation. The “chemistry-based” approaches focus on the local interactions between the species for which chemical identity is critical, and describe coacervation as the result of competitive local binding interactions of monomers and salts. In this article, we show how these approaches complement each other by presenting recent approaches that take both physical and chemical effects into account. Finally, we suggest future directions toward producing theories that are made quantitatively predictive by accounting for both long range electrostatic and local chemically specific interactions.