Study of a Surface Plasmon Resonance Optical Fiber Sensor Based on Periodically Grating and Graphene

Silicon - In this paper an optical fiber sensor based on plasmonic resonance of graphene and periodically grating is designed and investigated. The proposed sensor consists of an optical fiber core...     

A new method to determine monomer concentration in the polymer particles of emulsion polymerization systems by dynamic light scattering

In the published article cited above, by considering corrections made on the eq. (19) which will be discussed in the next section, Figure 6 should be replaced with a following new Figure 1. Hence, and values of 0.379 and 5.68 mol.dm^?3, respectively, on pages 1055, 1061, and 1062 should be changed to their accurate values of 0.426 and 5.29 mol.dm^?3, respectively.     

Effect of the carboxylic acid monomer type on the emulsifier‐free emulsion copolymerization of styrene and butadiene

Carboxylated styrene–butadiene rubber latexes were prepared through the emulsifier‐free emulsion copolymerization of styrene and butadiene with various carboxylic acid monomers. The effects of various carboxylic acid monomers on the particle formation process were investigated. The type of carboxylic acid monomer strongly affected the particle nucleation. The number of particles and thus the polymerization rate increased with the increasing hydrophobicity of the carboxylic acid monomers. There was a significant difference in the polymerization rate per particle. The results showed that particle nucleation and growth were dependent on the hydrophilic nature of the carboxylic acid monomers. The average particle diameter of the carboxylated styrene–butadiene rubber latexes in the dry state was obtained through some calculations using direct measurements of the average particle diameter in the monomer‐swollen state by a dynamic light scattering technique. Several parameters, such as the polymerization rate, number of latex particles per unit of volume of the aqueous phase, and polymerization rate per particle, were calculated. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Numerical simulation of atomic layer deposition for thin deposit formation in a mesoporous substrate

ZnO deposition in porous γ-Al₂O₃ via atomic layer deposition (ALD) is the critical first step for the fabrication of zeolitic imidazolate framework membranes using the ligand-induced perm-selectivation process (Science, 361 (2018), 1008–1011). A detailed computational fluid dynamics (CFD) model of the ALD reactor is developed using a finite-volume-based code and validated. It accounts for the transport processes within the feeding system and reaction chamber. The simulated precursor spatiotemporal profiles assuming no ALD reaction were used as boundary conditions in modeling diethylzinc reaction/diffusion in porous γ-Al₂O₃, the predictions of which agreed with experimental electron microscopy measurements. Further simulations confirmed that the present deposition flux is much less than the upper limit of flux, below which the decoupling of reactor/substrate is an accurate assumption. The modeling approach demonstrated here allows for the design of ALD processes for thin-film membrane formation including the synthesis of metal–organic framework membranes.     

Chemical vapor deposition of poly(3‐alkylthiophene) nanoparticles on fabric: Chemical and electrochemical characterization

Chemical vapor deposition of poly(3‐methylthiophene) and poly (3‐hexylthiophene) as conductive polymers on the surface of polyester fabrics was successfully obtained. Fourier transform infrared spectroscopy confirmed the formation of polymers on surface of fabrics (the fingerprint of polythiophenes, υ 600–1500 cm^?1). The uniformity of deposition and nanoparticles (average size of 60 nm) were proved with scanning electron microscopy. Electrochemical impedance spectroscopy showed that P3HT‐coated samples offer higher conductivity in compared to P3MT‐coated samples. The impedance modulus of P3HT‐coated samples was lowered nine times to that of row materials and reached to c8000 Ω. The samples have also shown electrochromic properties under electrical current, changing its color from yellowish green at 0 V to dark green at +12 V for poly (3‐hexylthiophene) samples and from brown at 0 V to red at +12 V for poly(3‐methylthiophene)‐coated fabrics (V = 0 V, λ = 450 nm; V = 12 V, λ = 650 nm). © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40673.     

Influence of Ni/Co binders and Mo2C on the microstructure evolution and mechanical properties of (Ti0.93W0.07)C–based cermets

In this research, solid–solution powder of (Ti_0.93W_0.07)C was synthesized by high–energy ball mill method followed by carbothermal reduction process. Subsequently, the acquired powder was blended with Ni/Co and Mo₂C secondary carbide, and sintered under the optimized temperature (1510?°C) for 1?h to produce the modulated cermets. A typical core–rim structure formation with solid–solution phases was confirmed by backscattered electrons studies using a Field Emission electron scanning microscope. The hardness of the synthesized cermets was enhanced by increasing the specific amount of Mo₂C. The acquired results demonstrate that the binder type has a prominent influence on the microstructure and hardness of the prepared cermets. The hardness of (Ti_0.93W_0.07)C–xMo₂C–Ni cermet increased ~ 9%, when nickel was partially substituted by cobalt.     

Mathematical Modeling of a Simulated Moving‐Bed Adsorption Process: Parex™ Technology as a Case Study

A simplified dynamic mathematical model for a simulated moving‐bed adsorption process is presented. The model is adopted to simulate the separation process of p‐xylene from the other 8‐carbon aromatics by means of the Parex^? technology. Operating conditions and the moving‐bed structure for a commercial plant were used and the performance of the unit was simulated. The model results are in good agreement with the findings of similar existing studies. Comparison of the results of this simplified model with those obtained by other researches indicates a considerable decrease in central processing unit (CPU) time.     

Reverse iodine transfer polymerization of vinyl acetate and vinyl benzoate: synthesis and characterization of homo‐ and copolymers

Homo‐ and copolymers of vinyl esters including vinyl acetate (VAc) and vinyl benzoate (VBz) were synthesized via the reverse iodine transfer radical polymerization technique. Polymerization was carried out in the presence of iodine as the in situ generator of the transfer agent and 2,2′‐azobis(isobutyronitrile) as the initiator at 70 °C. Reverse iodine transfer radical homopolymerization of VAc and VBz led to conversions of 76 and 57%, number‐average molecular weights of 8266 and 9814 g mol^?1 and molecular weight distributions of 1.58 and 1.49, respectively. The microstructure of the synthesized polymers was investigated in detail using gel permeation chromatography, ¹H NMR, ¹³C NMR and distortionless enhancement of polarization transfer (135° decoupler pulse) techniques. Relatively narrow molecular weight distribution and controlled and predictable trend of molecular weight versus conversion were observed for the synthesized polymers, showing that reverse iodine transfer radical homo‐ and copolymerization of VAc and VBz proceeded with controlled characteristics. Results of molecular weight and its distribution along with the ¹H NMR spectra recorded for homo‐ and copolymers indicated that side reactions can occur during the course of polymerization with a significant contribution when VAc, even in a small amount, was present in the reaction mixture. This can result in polymer chains with aldehyde dead end and broadening of the molecular weight distribution. © 2015 Society of Chemical Industry     

Geochemical modeling and experimental evaluation of high-pH floods: Impact of Water–Rock interactions in sandstone

Injection of alkaline solutions in reservoir leads to mineral dissolution and precipitation, possibly resulting in changes in permeability and porosity, and consequently altering solution pH. Accurate prediction of pH, alkali consumption and aqueous chemistry changes are required to design suitable chemical blends in alkaline-polymer (AP) or alkaline-surfactant-polymer (ASP) flooding. Excessive consumption of alkali can result in degradation of flood performance and lower than expected oil recovery. We report state-of-the-art geochemical simulation results for sandstone reservoir mineral assemblages and alkali solutions (NaOH, Na₂CO₃, and NaBO₂) employed in AP and ASP formulations. Single-phase high-pH corefloods were completed using Berea sandstone and reservoir samples to calibrate and validate geochemical simulations. Results show that rock-fluid interactions depend strongly on mineral type and amount, alkaline solution injection flowrate, and composition of the injected and formation water. Anhydrite, a commonly found calcium sulfate, significantly impacts pH buffering capacity, water chemistry and permeability damage against conventional alkali agents in chemical flooding particularly for Na₂CO₃, but no significant pH buffering is observed during NaBO₂ flooding. Experimental data and model results show that the pH-buffering effect is maintained even after several pore volumes of alkaline solution are injected, if a sufficient fraction of relevant minerals is present. The end consequence of this is insufficient alkalinity for reactions with the oil phase and the likely formation damage.     

Fabricating Janus membranes via physicochemical selective chemical vapor deposition

Membranes with asymmetric wettability-Janus membranes-have recently received considerable attention for a variety of critical applications. Here, we report on a simple approach to introduce asymmetric wettability into hydrophilic porous domains. Our approach is based on the physicochemical-selective deposition of polytetrafluoroethylene (PTFE) on hydrophilic polymeric substrates. To achieve selective deposition of PTFE, we inhibit the polymerization reaction within the porous domain. We prefill the substrates with glycerol, containing a known amount of free radical inhibitor, and utilize initiated chemical vapor deposition (iCVD) for the polymerization of PTFE. We show that the glycerol/inhibitor mixture hinders the deposition of PTFE within the membrane pores. As a result, the surface of the substrates remains open and porous. The fabricated Janus membranes show stable wetting-resistant properties, evaluated through sessile drop contact angle measurements and direct contact membrane distillation (DCMD).