Degradation of Remazol Black B dye and its simulated dyebath wastewater by advanced oxidation processes in heterogeneous and homogeneous media

This study focused on the degradation of hydrolysed Remazol Black B (CI Reactive Black 5), a common diazo reactive dye, in aqueous solution. In the presence of various dye auxiliary chemicals a typical Remazol Black exhausted dyebath liquor simulated, which was then treated with homogeneous [ozonation with hydroxy ions, and Fe(II) or Fe(III) with hydrogen peroxide] and heterogeneous (titanium dioxide with UV-A irradiation) advanced oxidation processes. Treatment performance of the investigated advanced oxidation systems was comparatively assessed in terms of the environmental sum parameters total organic carbon, biochemical oxygen demand and spectrophotometric measurements. The results obtained clearly reveal that the investigated advanced oxidation processes are capable of completely decolourising and partially mineralising the dye solution and its simulated dyebath effluent under predetermined reaction conditions. During the application of alkaline ozonation at an ozone dose of 2340 mg/ml, a three-fold biodegradability enhancement was observed.     

Coherent MAP detection of DQPSK bits

Both IS-136 and PDC digital cellular systems employ forward error correction (FEC) encoding followed by a form of DQPSK modulation. In this letter, we derive the maximum a posteriori (MAP) bit detector for DQPSK modulation in non-ISI channels for a coherent receiver with one or more antennas. The MAP detector forms a bit log-likelihood ratio, which provides the optimal “soft information” for MLSE or MAP convolutional decoding. MAP detection requires exponentiation and logarithm operations, as well as knowledge of the noise covariance. To avoid these operations, two approximate forms are developed, which do not require the noise covariance value under certain assumptions. Both approximate approaches, when used with soft FEC decoding, are within 0.5 dB of the optimal approach     

Analysis of the influence of crushing on the behavior of granular materials under shear

The behavior of granular materials mainly depends on the mechanical and engineering properties of particles in its structural matrix. Crushing or breakage of granular materials under compression or shear occurs when the energy available is sufficient to overcome the resistance of the material. Relatively little systematic research has been conducted regarding how to evaluate or quantify particle crushing and how it effects the engineering properties of the granular materials. The aim of this study is to investigate the effect of crushing on the bulk behavior of granular materials by using manufactured granular materials (MGM) rather than using a naturally occurring cohesionless granular material. MGM allow changing only one particle parameter, namely the “crushing strength”. Four different categories of MGM (with different crushing strength) are used to study the effect on the bulk shear strength, stiffness modulus, friction and dilatancy angle “engineering properties”. A substantial influence on the stress–strain behavior and engineering properties of granular materials is observed. Higher confining stress causes some non-uniformity (strong variations/jumps) in volumetric strain and a constant volumetric strain is not always observed under large shear deformations due to crushing, i.e. there is no critical state with flow regime (with constant volumetric strain).     

Selective removal of Cr(VI) ions from aqueous solutions including Cr(VI), Cu(II) and Cd(II) ions by 4-vinly pyridine/2-hydroxyethylmethacrylate monomer mixture grafted poly(ethylene terephthalate) fiber

In this study, a new reactively fibrous adsorbent was prepared by grafting 4-vinly pyridine (4-VP) and 2-hydroxyethylmethacrylate (HEMA) monomer mixture onto poly(ethylene terephthalate) (PET) fibers for removal of Cr(VI), Cu(II) and Cd(II) metal ions from aqueous solution by using batch adsorption method. The influence of various parameters such as graft yield (GY), pH, adsorption time, initial ion concentration and adsorption temperature was investigated. The selectivity of the reactive fiber was also examined. The results show that the adsorbed amount of metal ions followed as given in the order Cr(VI) > Cd(II) > Cu(II). At pH 3, Cr(VI) was removed by 99% while the initial concentration of ions was at 5 mg L⁻¹ and by 94% at 400 mg L⁻¹. It was found that the grafted fiber is more selective for Cr(VI) ions in the mixed solution of Cr(VI)–Cu(II), Cr(VI)–Cd(II) and Cr(VI)–Cu(II)–Cd(II) at pH 3 and it was observed that the grafted fibers are stable and regenerable by acid and base without losing their activity.     

Tribological Characteristics of Calophyllum inophyllum–Based TMP (Trimethylolpropane) Ester as Energy-Saving and Biodegradable Lubricant

The purpose of this research is an experimental study of Calophyllum inophyllum (CI)-based trymethylolpropane (TMP) ester as an energy-saving and biodegradable lubricant and compare it with commercial lubricant and paraffin mineral oil using a four-ball tribometer. CI-based TMP ester is a renewable lubricant that is nonedible, biodegradable, and nontoxic and has net zero greenhouse gases. The TMP ester was produced from CI oil, which has high lubricity properties such as higher density, higher viscosity at both 40°C and 100°C and higher viscosity index (VI). Experiments were conducted during 3,600 s with constant load of 40 kg and constant sliding speed of 1,200 rpm at temperatures of 50, 60, 70, 80, 90, and 100°C for all three types of lubricant. The results show that CI TMP ester had the lowest coefficient of friction (COF) as well as lower consumption of energy at all test temperatures, but the worn surface roughness average (R_a) and wear scar diameter were higher compared to paraffin mineral oil and commercial lubricant. Before 80°C, CI TMP ester actually has a higher flash temperature parameter (FTP) than paraffin mineral oil and as the temperature increases, the FTP of TMP ester decreases. The worn surfaces of the stationary balls were analyzed by scanning electron microscopy (SEM) and results show that CI TMP ester has the highest wear compared to paraffin mineral oil and lowest wear compared to commercial lubricant. However, CI TMP ester is environmentally desired, competitive to commercial lubricant, and its use should be encouraged.     

Preparation and application of glycidyl methacrylate and methacrylic acid monomer mixture‐grafted poly(ethylene terephthalate) fibers for removal of methylene blue from aqueous solution

A novel fibrous adsorbent that grafts glycidyl methacrylate (GMA) and methacrylic acid (MAA) monomer mixture onto poly(ethylene terephthalate) (PET) fibers was used for removal of methylene blue (MB) in aqueous solutions by a batch equilibration technique. The operation parameters investigated included, pH of solution, removal time, graft yield, dye concentration, and reaction temperature. The adsorption rate of MB is much higher on the MAA/GMA‐grafted PET fibers than on the ungrafted PET fibers. MB was removed 99% the initial dye concentration at 10 mg L⁻¹ and 93% at 200 mg L⁻¹ by monomers mixture‐grafted PET fibers. Pseudofirst order and pseudosecond order kinetic equations were used to examine the experimental data of different graft yield. It was found that the pseudosecond order kinetic equation described the data of dye adsorption on fibrous adsorbent very well. The experimental isotherms data were analyzed using Langmuir and Freundlich isotherm models. The data was that Freundlich isotherm model fits the data very well for the dyes on the fibers adsorbent. The dye adsorbed was easily desorbed by treating with acetic acid/methanol mixture (50% V/V) at room temperature. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

The synthesis of poly(3‐hydroxybutyrate)‐g‐poly(methylmethacrylate) brush type graft copolymers by atom transfer radical polymerization method

Brush type of poly (3‐hydroxy butyrate), PHB, copolymer synthesis has been reported. Natural PHB was chlorinated by passing chlorine gas through PHB solution in CHCl₃/CCl₄ mixture (75/25 v/v) to prepare chlorinated PHB, PHB‐Cl, with the chlorine contents varying between 2.18 and 39.8 wt %. Toluene solution of PHB‐Cl was used in the atom transfer radical polymerization (ATRP) of methyl methacrylate, MMA, in the presence of cuprous bromide (CuBr)/2,2′‐bipyridine complex as catalyst, at 90°C. This “grafting from” technique led to obtain poly (3‐hydroxybutyrate)‐g‐poly(methylmethacrylate) (PHB‐g‐PMMA) brush type graft copolymers (cylindrical brush). The polymer brushes were fractionated by fractional precipitation methods and the γ values calculated from the ratio of the volume of nonsolvent to volume of solvent of brushes were ranged between 2.8 and 9.5 depending on the molecular weight, grafting density, and side chain length of the brushes, while the γ values of PHB, PHB‐Cl, and homo‐PMMA were 2.7–3.8, 0.3–2.4, and 3.0–3.9, respectively. The fractionated brushes were characterized by gel permeation chromatography, ¹H‐NMR spectrometry, thermogravimetric analysis (TGA), and differential scanning calorimetry techniques. PHB‐g‐PMMA brush type graft copolymers showed narrower molecular weight distribution (mostly in range between 1.3 and 2.2) than the PHB‐Cl macroinitiator (1.6–3.5). PHB contents in the brushes were calculated from their TGA thermograms and found to be in range between 22 and 42 mol %. The morphologies of PHB‐g‐PMMA brushes were also studied by scanning electron microscopy. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Synthesis and spectroelectrochemistry of dithieno(3,2‐b:2′,3′‐d)pyrrole derivatives

New π‐conjugated polymers containing dithieno(3,2‐b:2′,3′‐d)pyrrole (DTP) were successfully synthesized via electropolymerization. The effect of structural differences on the electrochemical and optoelectronic properties of the 4‐[4H‐dithieno(3,2‐b:2′,3′‐d)pyrrol‐4‐yl]aniline (DTP–aryl–NH₂), 10‐[4H‐dithiyeno(3,2‐b:2′,3′‐d)pirol‐4‐il]dekan‐1‐amine (DTP–alkyl–NH₂), and 1,10‐bis[4H‐dithieno(3,2‐b:2′,3′‐d)pyrrol‐4‐yl] decane (DTP–alkyl–DTP) were investigated. The corresponding polymers were characterized by cyclic voltammetry, NMR (¹H‐NMR and ¹³C‐NMR), and ultraviolet–visible spectroscopy. Changes in the electronic nature of the functional groups led to variations in the electrochemical properties of the π‐conjugated systems. The electroactive polymer films revealed redox couples and exhibited electrochromic behavior. The replacement of the DTP–alkyl–DTP unit with DTP–aryl–NH₂ and DTP–alkyl–NH₂ resulted in a lower oxidation potential. Both the poly(10‐(4H‐Dithiyeno[3,2‐b:2′,3′‐d]pirol‐4‐il)dekan‐1‐amin) (poly(DTP–alkyl–NH₂)) and poly(1,10‐bis(4H‐dithieno[3,2‐b:2′,3′‐d]pyrrol‐4‐yl) decane) (poly(DTP–alkyl–DTP)) films showed multicolor electrochromism and also fast switching times (<1 s) in the visible and near infrared regions. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40701.