Utilization of Some Egyptian Waste Kaolinitic Sand as Grog for Bricks and Concrete

The aim of the present study is to assess the suitability of some waste kaolinitic sand as grog for bricks and concretes. Three samples were selected and their chemical and mineralogical compositions as well as their ceramic and mechanical properties were investigated. The solid phase composition as well as the microstructure of the vitrified samples was also carried out using XRD and SEM methods. Refractoriness under load and thermal shock resistance are also investigated. Chemical and phase composition confirm that two samples (1 and 2) are fireclay with total impurities oxide contents (TIOC) less than 3.0 % while the third is mainly silica with TIOC less than 0.5 %. The microstructure of samples 1 and 2 shows predominant mullite crystals, bonded by silicate phases as confirmed by XRD, whereas silica phases are the main components of the third sample with minor intercalation of mullite phase. It is concluded that samples 1 and 2 fired at 1500 ?C can be used as grog for brick and concrete manufacture in industrial furnaces up to 1400 °C while sample 3 needs some additives to form denser grains.     

Exploiting the Plackett–Burman design to examine the formulation effect on curing characteristics of oil palm ash-filled acrylonitrile butadiene rubber compounds

The present paper is focused on exploiting Plackett–Burman design to examine the formulation effect of various chemical components content on the curing characteristics of oil palm ash (OPA)-filled acrylonitrile butadiene rubber (NBR) compound. The filled-NBR compound was prepared by conventional laboratory-sized two roll mill and cured using sulfuric system. Six independent variables such as content of zinc oxide, stearic acid, N-isopropyl-N′-phenyl-p-phenylenediamine, N-cyclohexyl-2-benzothiazole sulfenamide (CBS), sulfur, and even OPA filler were carried out to screen their significant effect on the curing characteristics of NBR compound. The scorch time, optimal cure time, minimum torque, and maximum torque were selected as a response. Results showed that the scorch time and the optimal cure time were significantly affected by CBS, whereas the minimum torque and maximum torque were significantly affected by OPA and sulfur, respectively, within the studied range. Among the chemical components under study, zinc oxide and stearic acid had the least effect on the curing properties of NBR compound. Analysis of variances for all factorial models demonstrated that the model was significant with P value <0.05 while the regularity (R ²) of all models was greater than 0.9. Lastly, the optimal chemical concentrations were predicted to acquire the optimal condition of the curing system for filled-NBR compound.     

Improving Blood Compatibility of Polyethersulfone Hollow Fiber Membranes via Blending with Sulfonated Polyether Ether Ketone

Appropriate membrane for blood contacting applications requires hemocompatibility and high permeation flux; it should inhibit proteins or platelets adsorption and still possess high permeability. Aiming to improve the polyethersulfone (PES) hollow fiber membrane hemocompatibility, sulfonated polyether ether ketone (SPEEK) is self‐synthesized in the present research and added to PES in different ratios. Scanning electron microscopy images have revealed significant changes in PES membranes structure after addition of SPEEK, which can influence water permeation property of the membranes. Water contact angles of the membranes have reduced from 75° to 50° after addition of 4 wt% SPEEK. Influence of SPEEK addition on hemocompatibility of the PES membranes is evaluated via protein (bovine serum albumin) adsorption, platelet attachment, and coagulation time (APTT and TT) assays. Obtained results reveal that hemocompatibility of the modified hollow fiber membranes is enhanced as a result of emerging repulsive forces between negative charges on the membranes surface and negatively charge blood components.

     

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     

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.

     

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.

     

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.     

Design and analysis of a new magneto rheological damper for washing machine

In this article, a new magneto rheological (MR) sponge damper is proposed for suppression of vibrations in a washing machine. The article presents design optimization of geometric parameters of MR sponge damper (MRSD) using the finite element analysis (FEA) and first order derivative techniques for a washing machine. The article explains the hysteresis behavior and the relationship of damping force with input current for the proposed MRSD. Moreover, the characteristics of the MRSD such as energy dissipation and equivalent damping coefficient are investigated experimentally in terms of input current and excitation amplitude. The passive dampers installed in washing machine are ineffective in reducing unwanted vibrations at resonant frequencies due to real time unbalanced mass. For this purpose, a test setup is established in order to compare the performance of passive dampers with the proposed MRSDs in a washing machine. It is noticed that MRSDs reduce average vibrations of 75.61 % in a low frequency band, whereas in a high frequency band, the MRSDs lessen average vibrations of 30.57 % in a washing machine. In order to determine the performance of proposed design MRSD, a detailed comparison of the performance parameters, such as total damping force, passive force, maximum average vibrations after suppression by MR dampers, maximum current and power ratings is provided with the existing designs of MR damper for washing machine from the literature.     

Influence of kenaf form and loading on the properties of kenaf‐filled polypropylene/waste tire dust composites: A comparison study

Kenaf (KNF)‐filled polypropylene/waste tire dust (PP/WTD) composites containing different KNF loadings (0, 5, 10, 15, and 20 parts per hundred parts of resin (phr)) were prepared using a Thermo Haake Polydrive internal mixer. The influence of the KNF form (KNF short fiber (KNFs) and KNF powder (KNFp)) at different KNF loadings on properties of the composites was studied. Results showed that with increasing KNF loading, the stabilization torque, tensile modulus, water absorption, and thermal properties increased for both KNFp‐ and KNFs‐filled PP/WTD composites. However, the tensile strength and elongation at break decreased by 29.2% and 53.9%, respectively, for KNFp‐filled PP/WTD composites, whereas KNFs‐filled PP/WTD composites showed a decrement of 24.5% and 63.5%, respectively. The stabilization torque, tensile strength, and tensile modulus increased by 22.4%, 6.7%, and 2.6%, respectively, for KNFs‐filled PP/WTD composites at 20 phr KNF loading. The scanning electron microscopy morphological studies on the tensile fractured surfaces revealed poor adhesion between KNFp and PP/WTD matrices as compared to KNFs and PP/WTD matrices. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40877.