15 research outputs found

    Iron oxychloride as an efficient catalyst for selective hydroxylation of benzene to phenol

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    Selective hydroxylation of benzene is a felicitous strategy for the production of phenol that is deemed to be an alternative to conventional processes. Thus, the development of a durable and highly efficient catalyst for the selective hydroxylation of benzene should be a key topic. In this work, FeOCl was prepared by a chemical vapor transition method and characterized using various techniques including XRD, TEM, Raman spectroscopy, N2 adsorption–desorption, DLS, and TGA. The prepared FeOCl was applied as a heterogeneous catalyst in benzene hydroxylation, and the reaction conditions were optimized. The acquired data manifested that FeOCl has shown superiority over the other reported catalysts utilized in benzene hydroxylation. The superiority of FeOCl is attributed to the facile self-redox potential of FeOCl and its remarkable ability for the production of an overwhelming amount of hydroxyl radicals in a short period of time. The catalyst recovery and reuse test showed that FeOCl is able to endure the harsh conditions of benzene hydroxylation for four runs. The mechanism of benzene hydroxylation using FeOCl as a catalyst in the presence of hydrogen peroxide as an oxidant was also illustrated

    Monitoring Moisture Damage Propagation in GFRP Composites Using Carbon Nanoparticles

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    Glass fiber reinforced polymer (GFRP) composites are widely used in infrastructure applications including water structures due to their relatively high durability, high strength to weight ratio, and non-corrosiveness. Here we demonstrate the potential use of carbon nanoparticles dispersed during GFRP composite fabrication to reduce water absorption of GFRP and to enable monitoring of moisture damage propagation in GFRP composites. GFRP coupons incorporating 2.0 wt % carbon nanofibers (CNFs) and 2.0 wt % multi-wall carbon nanotubes (MWCNTs) were fabricated in order to study the effect of moisture damage on mechanical properties of GFRP. Water absorption tests were carried out by immersing the GFRP coupons in a seawater bath at two temperatures for a time period of three months. Effects of water immersion on the mechanical properties and glass transition temperature of GFRP were investigated. Furthermore, moisture damage in GFRP was monitored by measuring the electrical conductivity of the GFRP coupons. It was shown that carbon nanoparticles can provide a means of self-sensing that enables the monitoring of moisture damage in GFRP. Despite the success of the proposed technique, it might not be able to efficiently describe moisture damage propagation in GFRP beyond a specific threshold because of the relatively high electrical conductivity of seawater. Microstructural investigations using Fourier Transform Infrared (FTIR) explained the significance of seawater immersion time and temperature on the different levels of moisture damage in GFRP

    Synthesis and evaluation of some amine compounds having surface active properties as H2S scavenger

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    In this work three H2S scavengers were prepared by reacting monoethanolamine with formaldehyde in different ratios (1:1, 2:1 and 2:3) to give MF1, MF2 and MF3, respectively. The chemical structures of the prepared scavengers were confirmed by FT-IR spectroscopy. The effect of reaction time (the time required for completing the reaction between the scavenger and the H2S gas) has been studied for the three prepared scavengers. The effects of concentration and temperature have been studied on the scavenging efficiency of H2S using three prepared products and two commercial products EPRI-710 and EPRI-730. The surface and thermodynamic parameters of the prepared scavengers were determined at 25 °C including, surface tension (γ), and effectiveness, maximum surface excess (Γmax) and minimum surface area (Amin). Also, the standard free energy of micellization and adsorption was recorded. The results show that the efficiency of scavengers increased with increasing reaction time up to 50 min. Also, as concentration of scavengers and temperature increased, the removal efficiency of the scavengers increased. By comparing the efficiency of the prepared products with the commercial products EPRI-710 and EPRI 730, it was found that, MF3 exhibited a similar efficiency comparing with the commercial scavenger EPRI 730 (currently used in the field) at different concentrations and temperatures

    Structure effect of some amine derivatives on corrosion inhibition efficiency for carbon steel in acidic media using electrochemical and Quantum Theory Methods

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    The structure effect on corrosion inhibition of two amines and their derivatives is the main object of this article. The first amine was 1,8-diaminooctane and its ethoxylated (50 e.o.) 1,8-diaminooctane and propoxylated (50 p.o.) 1,8-diaminooctane. The second amine is the tetraethylenepentamine and its ethoxylated (50 e.o.) and propoxylated (50 p.o.) derivatives. The investigations were carried out by open circuit potential, potentiodynamic polarization, electrochemical impedance, quantum calculations and SEM measurements. The data obtained for the first amine showed the minimum inhibition efficiency (65.5%), meanwhile the maximum inhibition efficiency was 78.9% for its propoxylated derivative. On the other hand the maximium inhibition efficiency was 91% for the second propoxylated amine. The electronic properties; HOMO and LUMO energy levels, energy gap, dipole moment, polarizability, log P, total energy, charge densities, area/molecule and hydration energy have been calculated. The inhibition efficiency was calculated theoretically using the electronic parameters. From the obtained results, there is a significant difference between the inhibition efficiency of the electronic and the inhibition efficiency experimentally. The results were discussed on the light of the chemical structure of the used inhibitors. In general, the inhibition efficiency is affected by the shape and structure of the molecule

    Synthesis and evaluation of some new demulsifiers based on bisphenols for treating water-in-crude oil emulsions

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    The present paper endeavors to synthesize nine types of demulsifiers based on bisphenols (bisphenol A (BA), bisphenol AC (BAC) and bisphenol CH (BCH)) having different ethylene oxide units (n = 27, 34, 45) namely; E (x + y) (where E represents BA, BCH or BAC and (x + y) which represents the ethylene oxide units (27, 34, 45)). The chemical structures of the prepared demulsifier were elucidated using FT-IR and 1H NMR spectra. Effect of the chemical structure (hydrophobic and ethoxylated degree of hydrophilic parts) and the mechanism of demulsification process was investigated. The data were discussed on the light of the chemical structure of the demulsifiers and the factors, effecting the demulsification process. The efficiency of these demulsifiers was tested on water-in-oil emulsions (w/o) at different concentrations (100, 200 and 300 ppm), 7.4% asphaltene content and 30%, 50% and 70% water content. From the obtained data the best demulsifier was E(34)BA which shows 100% demulsification after 58 min at 30% water content and 300 ppm of the demulsifier

    Catalytic performance of organically templated nano nickel incorporated-rice husk silica in hydroconversion of cyclohexene and dehydrogenation of ethanol

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    Rice husk silica (RHS) was extracted from local rice husk by acid digestion and burning at 650 °C. RHS-Ni catalyst was prepared by dissolving RHS in 1 N NaOH and titrating with 3 N HNO3 containing 10 wt.% Ni2+. The organic modifiers, either p-amino benzoic acid (A) or p-phenylenediamine (PDA) were incorporated in 5 wt.% and reduced in H2 flow. Investigation of the three catalysts, (RHS-Ni)R350, (RHS-Ni–A)R350 and (RHS-Ni–PDA)R350, confirmed good dispersion of Ni nanoparticles; all catalysts were amorphous. The BET surface areas increased in the order: (RHS-Ni)R350  150 °C, the backward dehydrogenation pathway was more favored, due to unavailability of H2; the process became structure-sensitive. In ethanol conversion, the prevailing dehydrogenation activity of organically modified catalyst samples was encouraged by improved homogeneous distribution of Ni nanoparticles and created micropre system

    Glycolysis of Poly(ethylene terephthalate) Catalyzed by the Lewis Base Ionic Liquid [Bmim][OAc]

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    The glycolysis of poly­(ethylene terephthalate) (PET) was studied using 1-butyl-3-methylimidazolium acetate ([Bmim]­[OAc]) as a catalyst. The effects of temperature, time, ethylene glycol dosage, PET amount, and [Bmim]­[OAc] dosage on the glycolysis reaction were examined. The results revealed that [Bmim]­[OAc] has a PET conversion of 100% and a bis­(2-hydroxyethyl)­terephthalate (BHET) yield of 58.2% under the optimum conditions of 1.0 g of [Bmim]­[OAc] with 20 g of ethylene glycol in the presence of 3.0 g of PET at 190 °C after 3 h of glycolysis. The ionic liquid could be reused up to six times with no apparent decrease in the conversion of PET or yield of BHET. The pH plays a major role in explaining the proposed mechanism of glycolysis using the Lewis base ionic liquid [Bmim]­[OAc]. The kinetics of the reaction was first-order with an activation energy of 58.53 kJ/mol

    Molecular characterization of fowl aviadenoviruses species D and E associated with inclusion body hepatitis in chickens and falcons indicates possible cross-species transmission

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    <p>During the period from 2015 to 2017, frequent outbreaks of inclusion body hepatitis (IBH) were observed in broiler chickens and falcons in Saudi Arabia. Fifty samples were collected from both species. The histopathological examination and polymerase chain reaction confirmed the IBH infection in eight samples (five samples from chickens and three samples from falcons). The genomic sequence and phylogenetic analysis based on nucleotide and amino acid sequences of Saudi strains, reference fowl aviadenoviruses (FAdVs) and field viruses available in Genbank revealed that all investigated FAdVs clustered into FAdV-2 (species D) and FAdV-6 (species E). The host-dependent characterization revealed that falcon origin strains showed low identity (∼35%) with falcon adenoviruses isolated from USA, which clustered into a separate group. The identification of FAdV-D and FAdV-E in diseased falcons and chickens indicates cross-species transmission although falcons and chickens are phylogenetically different. The control of IBH infection in falcons and chickens should be based on the separation of carriers and susceptible chickens as well as falcons to prevent cross-species contact. Vaccination is an important method for prevention of IBH. The characterization of newly emerging FAdV strains provides valuable information for the development of an efficacious control strategy based on the molecular structure of current circulating FAdV strains in different species of birds.</p
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