Crevice corrosion behavior of high-alloy stainless steelsin a SWRO pilot plant

This paper presents the results of a study which has been carried out to investigate the crevice corrosion behavior of high-alloy stainless steel in a SWRO pilot plant. The study evaluated the corrosion performance of some austenitic and duplex steels in a crevice-forming environment created in a RO plant, especially in high-pressure feed and brine lines. The study of the effect of chemical dosing on crevice corrosion in the RO plant and electrochemical testing of crevice corrosion in the laboratory were the main objectives of this test program. High-alloy stainless steels, namely AL 6XN® and 254 SMO (superaustenitic), 2205, 2507 and DP3W (Duplex) were used in the test program. The tests were carried out in natural seawater and RO concentrate (conductivity: 75,000 to 80,000 μS/cm) at ambient temperature by operating the test plant at normal SWRO operating feed pressure of 54 bar. FeCl₃ was added as coagulant to maintain a silt density index of ∼3, and H₂SO₄ was added to feed in order to maintain the feed pH of ∼ 6.5. Chlorination and subsequent dechlorination agents were not added to the feed. For crevice corrosion tests in RO unit, the exposure periods were 6 and 12 months, respectively. The results of the tests showed that alloy DP3W has the best pitting resistance in crevice forming environment of seawater. In RO concentrate, alloys 2507 and 254 SMO showed lowest “maximum pit depth”. The results of potentiodynamic cyclic polarization (PCP) indicate that all the alloys have high pitting potential and small hysteresis loop. The results of critical crevice solution pH (CCSpH) indicated excellent resistance of alloys 254 SMO and DP3W against crevice corrosion attack and 2205 had least resistance in most aggressive sodium chloride solution.     

Preparation of nanostructured PbI2/Si photodetector by magnetic field-assisted laser ablation in liquid

Silicon - In this study, we report the synthesis of lead iodide PbI2 nanoparticles (NPs) by magnetic field-assisted pulsed laser ablation in ethanol. Results of X-ray diffraction (XRD) show that...     

Synthesis of HgI2 Nanoparticles and Nanorods by Laser Ablation in Liquid for Photodetector Applications: Effect of Laser Fluence

In this study, mercury iodide (HgI₂) nanoparticles (NPs) were synthesized by pulsed laser ablation in ethanol at laser fluences of 22.9, 33.1, and 43.3 J/cm². The effect of laser fluence on the structural and optical properties of HgI₂ NPs was studied. X-ray diffraction findings reveal that all synthesized HgI₂ samples were polycrystalline in nature with orthorhombic structure. Absorption peak was appeared at 474 nm and the optical energy gap of HgI₂ NPs decreases from 2.13 to 2.05 eV as laser fluence increased from 22.9 to 43.3 J/cm². Zeta potential (ZP) results confirm that the nanoparticles synthesized at 22.9 and 33.1 J/cm² have high degree of stability. Fluorescence measurements show the presence of several emission bands. Raman spectra of HgI₂ NPs show the presence of six vibration modes centered at 15, 29, 37, 44, 51, and 70 cm^?1. Fourier transform infrared (FT-IR) results show the presence of two bonds, namely, C–O and Hg-I. Transmission Electron Microscope (TEM) results showed that the formation of spherical nanoparticles for sample prepared at 22.9 J/cm², 25–75 nm in size. While the nanoparticles synthesized with 33.1 and 43.3 J/cm² exhibit nanorods and nanotubes morphologies, respectively. The dark I–V characteristics of β-HgI₂ NPs/Si heterojunction photodetectors show rectification properties and the junction quality depends on the laser fluence and the best junction characteristics was obtained for heterojunction prepared at 33.1 J/cm². The white light photosensitivity of the HgI₂/p-Si photodetectors was measured at reverse bias under different intensities. The maximum responsivity reached was 3.39A/W at 450 nm for photodetector prepared at 33.1 J/cm².

     

Synthesis and Characterization of Magnetically Retrievable Fe3O4/Polyvinylpyrrolidone/Polystyrene Nanocomposite Catalyst for Efficient Catalytic Oxidation Degradation of Dyes Pollutants

Recently, the application of metal oxides such as Fe₃O₄ nanoparticles have wide interest for environmental remediation and treatment of wastewater especially contaminated with azo dyes owing to its high degradation efficacy and low toxicity. The recovery of magnetic catalysts without losing their efficiency is an essential feature in the catalytic applications. The aim of this article is to investigate and synthesis of magnetically retrievable Fe₃O₄/polyvinylpyrrolidone/polystyrene (Fe₃O₄/PVP/PS) nanocomposite for the catalytic degradation of azo dye acid red 18 (AR18). Fe₃O₄/PVP/PS nanocomposite was prepared in two steps. Firstly, PVP/PS microsphere was synthesized by γ-irradiation polymerization of styrene in presence of PVP solution. Secondly, deposition of Fe₃O₄ nanoparticles on PVP/PS microsphere was achieved by the alkaline co-precipitation of Fe³⁺/Fe²⁺ ions. The chemical structural and morphological properties of PVP/PS microsphere and Fe₃O₄/PVP/PS nanocomposite were examined by XRD, TEM, DLS, FTIR, EDX and VSM techniques. TEM results showed homogeneous morphology, spherical shaped and well-dispersed Fe₃O₄ nanoparticles with average particle size of 26 nm around PVP/PS microspheres. The VSM measurements of Fe₃O₄/PVP/PS nanocomposite exhibit excellent magnetic response of saturation magnetization 26.38 emu/g which is suitable in magnetic separation. The effect of the synthesized Fe₃O₄/PVP/PS nanocomposite on the catalytic degradation of AR18 in presence of hydrogen peroxide (H₂O₂) as a heterogeneous Fenton-like catalyst was examined. The catalyst Fe₃O₄/PVP/PS/H₂O₂ played basic role in promoting the oxidation degradation efficiency of AR18 of initial concentration 50 mg/L to 94.4% in 45 min with excellent recyclability till the sixth cycles under the best conditions of pH 3, 2% v/v H₂O₂ and 0.3 g catalyst amount. Furthermore, the Fe₃O₄/PVP/PS/H₂O₂ hybrid catalyst system supports high capability for oxidation degradation of mixture of different dyes. The Fe₃O₄/PVP/PS nanocomposite catalyst had high magnetic and recyclability characters which are acceptable for the treatment of wastewater contaminated by various dyes pollutants.

     

Tunning the Physical Properties of PVDF/PVC/Zinc Ferrite Nanocomposites Films for More Efficient Adsorption of Cd (II)

This work deals with the synthesis of ZnFe₂O₄ NPs and studies the effect of addition on the physical properties PVDF/PVC blend. XRD affirmed the formation of ZnFe₂O₄ NPs and HRTEM shows that the size of the prepared ZnFe₂O₄ NPs ranged from 20 to 55 nm. The effect of ZnFe₂O₄ on the behavior of PVDF/PVC was studied through XRD, ATR-FTIR, FESEM and UV–Visible spectroscopy. XRD revealed that the addition of ZnFe₂O₄ NPs enhanced the crystallinity of PVDF/PVC blend system and also confirmed the incorporation of ZnFe₂O₄ NPs by appearing a diffraction peak at 2θ equals 35°. ATR-FTIR affirmed the interaction between blend sample and ZnFe₂O₄ NPs by appearing new bands 554 cm^?1 and 421 cm^?1 which are corresponded to ZnFe₂O₄ NPs functional group with appearing a new band at 603 cm^?1. FESEM showed that the addition of ZnFe₂O₄ to PVDF/PVC blend improved surface properties, for example, roughness average has been increased from 319 to 414 nm while maximum height increased from 260 to 473 nm for PVDF/PVC and PVDF/PVC/10% ZnFe₂O₄, respectively. Optical properties and band gap calculations revealed that addition of ZnFe₂O₄ NPs changes the structure of polyblend samples which results due to the formation of localized states. The removal efficiency of Cd (II) by using PVDF/PVC/10% ZnFe₂O₄ reached about 50% at pH 6 after 60 min. the absorption mechanism as well as kinetics isotherm have been studied. It is found that adsorption of Cd (II) occurred through the Langmuir mechanism and fellow pseudo-second order isotherm.

     

Surface-tailoring chlorine resistant materials and strategies for polyamide thin film composite reverse osmosis membranes

Polyamide thin film composite membranes have dominated current reverse osmosis market on account of their excellent separation performances compared to the integrally skinned counterparts. Despite their very promising separation performance, chlorine-induced degradation resulted from the susceptibility of polyamide toward chlorine attack has been regarded as the Achilles’s heel of polyamide thin film composite. The free chlorine species present during chlorine treatment can impair membrane performance through chlorination and depolymerization of the polyamide selective layer. From material point of view, a chemically stable membrane is crucial for the sustainable application of membrane separation process as it warrants a longer membrane lifespan and reduces the cost involved in membrane replacement. Various strategies, particularly those involved membrane material optimization and surface modifications, have been established to address this issue. This review discusses membrane degradation by free chlorine attack and its correlation with the surface chemistry of polyamide. The advancement in the development of chlorine resistant polyamide thin film composite membranes is reviewed based on the state-of-the-art surface modifications and tailoring approaches which include the in situ and post-fabrication membrane modifications using a broad range of functional materials. The challenges and future directions in this field are also highlighted.     

Effects of drilling parameters and aspect ratios on delamination and surface roughness of lignocellulosic HFRP composite laminates

Hemp fibre‐reinforced polycaprolactone (HFRP) composite has inherent good mechanical properties and benefits which include remarkably high specific strength and modulus, low density, and renewability. No doubt, these properties have attracted wider applications of HFRP composite in engineering applications. This paper presents an investigation on the influence of drilling parameters and fibre aspect ratios, AR (0, 19, 26, 30, and 38) on delamination damage factor and surface roughness of HFRP composite laminates utilising high speed steel twist drills under dry machining condition. Taguchi's technique was used in the design of experiment. The results obtained show that increase in cutting speed reduces delamination factor and surface roughness of drilled holes, whereas increase in feed rate causes increase in both delamination factor and surface roughness. Feed rate and cutting speed had the greatest influence on delamination and surface roughness respectively when compared with aspect ratio, while an increase in fibre aspect ratios leads to a significant increase in both delamination factor and surface roughness. The optimum results occurred at cutting speed and feed rate (drilling parameters) of 20 mm/min and 0.10 mm/rev, respectively, when drilling sample of AR 19. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 42879.     

Urethane‐forming reaction kinetics and catalysis of model palm olein polyols: Quantified impact of primary and secondary hydroxyls

Model palm olein natural oil polyols (NOPs) with varying ratios of primary to secondary hydroxyls were synthesized, characterized, and evaluated in reaction kinetics study with isocyanate in formation of polyurethanes. Reaction rate constants and activation energies associated with primary and secondary hydroxyls of NOPs were quantified. The kinetic study in toluene shows that the NOP containing primary hydroxyls have three times higher reaction rate constants in noncatalyzed reaction with 4,4′‐diphenylmethane diisocyanate (4,4′‐MDI) compared to the model NOP containing only secondary hydroxyls, which is associated with higher activation energy of secondary hydroxyls. However, the difference in reaction rate constants of primary and secondary hydroxyls in NOPs diminished in the reactions catalyzed with dibutyltin dilaurate. Bulk polymerization reaction confirms the kinetics results in toluene, showing that the model NOP containing primary hydroxyls reached gel time at a faster rate. Evaluation of elastomers from bulk polymerization shows low degree of phase separation of hard and soft segments for elastomers based on the model NOPs. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 42955.     

Effects of dynamic vulcanization on tensile,morphological, and swelling properties of poly(vinyl chloride) (PVC)/epoxidized natural rubber (ENR)/(Kenaf core powder) composites

The effects of dynamic vulcanization on properties of poly(vinyl chloride) (PVC)/epoxidized natural rubber (ENR)/(kenaf core powder) composite were studied. Tensile properties indicated that the strength, elongation at break, and Young's modulus of the composites exhibited an increase for samples with dynamic vulcanization. Morphological analysis using scanning electron microscopy showed the interaction between ENR and PVC. There was no bonding between kenaf core powder and the PVC/ENR matrix owing to the different polarity of both components. Filler agglomerates increased, which leads to an increase of filler‐filler interaction and poor dispersion. Furthermore, swelling index indicated that the composite with dynamic vulcanization shows lower absorption of tolune compared with composites without dynamic vulcanization. J. VINYL ADDIT. TECHNOL., 22:206–212, 2016. © 2014 Society of Plastics Engineers