Starch,Sucrose, and Rezol® IL800 as Density Modifiers for Polyurethane Rigid Foams Formulated by Recycled Polyol

Waste polyurethane rigid foam (PUF) is recycled by the glycolysis process. The recycled product is used in a polyol blend, applied in a new foam formulation. Polyurethane rigid foams formulated by recycled polyols are highly dense compared to rigid foams formulated by virgin polyols. As these foams are mostly used in insulation, they make an extra mass to the main product or system that is insulated. Therefore, it is important to decrease their density as much as possible.

Some density modifiers such as starch, sucrose, and REZOL^® IL800 were investigated to recognize their effect on PUF's density.     

A STUDY OF NON-NEWTONIAN FLOW AND HEAT TRANSFER OVER A NON-ISOTHERMAL WEDGE USING THE HOMOTOPY ANALYSIS METHOD

The thermoconvective boundary layer flow of a generalized third-grade viscoelastic power-law non-Newtonian fluid over a porous wedge is studied theoretically. The free stream velocity, the surface temperature variations, and the injection velocity at the surface are assumed variables. A similarity transformation is applied to reduce the governing partial differential equations for mass, momentum, and energy conservation to dimensionless, nonlinear, coupled, ordinary differential equations. The homotopy analysis method (HAM) is employed to generate approximate analytical solutions for the transformed nonlinear equations under the prescribed boundary conditions. The HAM solutions, in comparison with numerical solutions (fourth-order Runge-Kutta shooting quadrature), admit excellent accuracy. The residual errors for dimensionless velocity and dimensionless temperature are also computed. The influence of the “power-law” index on flow characteristics is also studied. The mathematical model finds important applications in polymeric processing and biotechnological manufacture. HAM holds significant promise as an analytical tool for chemical engineering fluid dynamics researchers, providing a robust benchmark for conventional numerical methods.     

Photocrosslinking of styrene–isoprene–styrene; effect of benzoin and ethylene glycol dimethacrylate on physical properties

Crosslinking reaction of polymer by ultraviolet (UV) irradiation has been important in industries. In this work, photocrosslinking of styrene–isoprene–styrene (SIS) triblock copolymer in the presence of benzoin photoinitiator and a dimethacrylate monomer as crosslinking agent was investigated. Curing of samples was initiated under UV irradiation. Benzoin was used as photoinitiator because it contains chromophore group that could absorb UV irradiation. Ethylene glycol dimethacrylate (EGDMA) was used as crosslinking agent, since it has alkene functional groups that could react with the alkene group of SIS. ATR-FTIR spectra of samples show that absorption band of double bond at 1500–1600?cm^?1 decreases after UV exposure. Increasing the concentration of benzoin (0.1–1?phr) and EGDMA (1–10?phr) leads to an increase in gel content and hardness, while swelling ratio decreases. After 5?min heating at 150?°C, about 20%wt of the unirradiated compound became insoluble, because heating of compound at 150?°C causes crosslinking reaction without any irradiation.     

Optimization of process parameters using D-optimal design for synthesis of ZnO nanoparticles via sol–gel technique

The experimental conditions for the synthesis of ZnO nanoparticles to produce minimal size were optimized using the D-optimal design. The influence of process parameters involves molar ratio of the starting materials, pH and the calcination temperature on the particle size were evaluated using the polynomial regression. The optimum conditions revealed by the model for obtaining a minimum particle size of ZnO were predicted to have a molar ratio of 1.76, pH of 1.50 and calcination at 402.2 °C. The obtainable particle size upon applying the model is 22.9 nm in compare to experimental result of 18 ± 2 nm was obtained.     

The calculations of dispersion coefficients inside two‐dimensional randomly packed beds of circular particles

The longitudinal (D_L) and transverse (D_T) dispersion coefficients in two‐dimensional (2‐D) randomly packed beds of circular particles in a laminar flow regime are derived. A 2‐D discrete system of particles is divided into cells using modified Voronoi diagrams. The relationship between the variation of the stream function and the averaged vorticity is obtained from computational fluid dynamics (CFD) simulations. The whole flow pattern is then obtained by using the principle of energy dissipation rate minimization. The obtained values of D_L agree well with 3‐D experimental data for all velocities investigated. At very high velocities, D_T in 2‐D appears to be higher than 3‐D experimental data. In addition, the effects of particle‐size distributions, packing structure, and porosity on the D_L and D_T were studied. One result was that an increase in the width of the particle‐size distribution resulted in higher values of D_L and D_T at high velocities. © 2012 American Institute of Chemical Engineers AIChE J, 59: 1002–1011, 2013     

Prediction of Hydrate Phase Equilibria in Aqueous Solutions of Salt and Organic Inhibitor Using a Combined Equation of State and Activity Coefficient‐Based Model

A thermodynamic model based on combination of the Valderrama modification of the Patel‐Teja equation of state with non‐density dependent mixing rules and a modification of a Debye‐Hückel electrostatic term is extended to systems containing salt and organic inhibitor by correcting the properties of the aqueous phase such as dielectric constant, density and molecular weight. A linear mixing rule is used for determining the dielectric constant of salt‐free mixture by introducing an interaction parameter (in dielectric constant mixing rule), which is tuned using the freezing point data of aqueous solutions containing salt and organic inhibitor. The binary interaction parameter between salt and organic inhibitor is adjusted using water vapour pressure data in the presence of salt and organic inhibitor. The predicted hydrate dissociation conditions are in acceptable agreement with the experimental data, demonstrating the reliability of the model developed in this work.     

Application of mesoporous magnetic carbon composite for reactive dyes removal: Process optimization using response surface methodology

Discharging the effluents of textile wastewaters into potable water resources can endanger the ecosystem, due to their reactivity, toxicity, and chemical stability. In this research, the application of powder activated carbon modified with magnetite nanoparticles (PAC-MNPs) as an adsorbent for removal of reactive dyes (Reactive black 5 (RB5) and reactive red 120 (RR120)) was studied in a batch system. The adsorption performance was evaluated as a function of temperature, contact time and different adsorbent and adsorbate concentrations. The levels of factors were statistically optimized using Box-Behnken Design (BBD) from the response surface methodology (RSM) to maximize the efficiency of the system. The adsorption process of both dyes was fit with the pseudo-second order kinetic and Langmuir isotherm models. The identified optimum conditions of adsorption were 38.7 °C, 46.3 min, 0.8 g/L and 102 mg/L for temperature, contact time, adsorbent dose, and initial dyes concentration, respectively. According to the Langmuir isotherm, the maximum sorption capacities of 175.4 and 172.4 mg/g were obtained for RB5 and RR120, respectively. Thermodynamics studies indicated that the adsorption process of the reactive dyes was spontaneous, feasible, and endothermic. After five cycles, the adsorption efficiency was around 84 and 83% for RB5 and RR120, respectively. A high value of desorption was achieved, suggesting that the PAC-MNPs have a good potential in regeneration and reusability, and also can be effectively utilized in industrial applications. PAC-MNPs also show a good anti-interference potential for removal of reactive dyes in dye-industry wastewaters.     

The morphology and gas‐separation performance of membranes comprising multiwalled carbon nanotubes/polysulfone–Kapton

The development of desirable chemical structures and properties in nanocomposite membranes involve steps that need to be carefully designed and controlled. This study investigates the effect of adding multiwalled nanotubes (MWNT) on a Kapton–polysulfone composite membrane on the separation of various gas pairs. Data from Fourier transform infrared spectroscopy and scanning electron microscopy confirm that some studies on the Kapton–polysulfone blends are miscible on the molecular level. In fact, the results indicate that the chemical structure of the blend components, the Kapton–polysulfone blend compositions, and the carbon nanotubes play important roles in the transport properties of the resulting membranes. The results of gas permeability tests for the synthesized membranes specify that using a higher percentage of polysulfone (PSF) in blends resulted in membranes with higher ideal selectivity and permeability. Although the addition of nanotubes can increase the permeability of gases, it decreases gas pair selectivity. Furthermore, these outcomes suggest that Kapton–PSF membranes with higher PSF are special candidates for CO₂/CH₄ separation compared to CO₂/N₂ and O₂/N₂ separation. High CH₄, CO₂, N₂, and O₂ permeabilities of 0.35, 6.2, 0.34, and 1.15 bar, respectively, are obtained for the developed Kapton–PSF membranes (25/75%) with the highest percentage of carbon nanotubes (8%), whose values are the highest among all the resultant membranes. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43839.     

The effects of long‐term exposure of flax fiber reinforced polymer to salt solution at high temperature on tensile properties

Most research on natural fiber composites has been primarily conducted on randomly‐oriented fibers. This study is focused on the short‐ and long‐term performances of flax fiber‐reinforced polymer (Flax‐FRP) made from continuous unidirectional fiber mats, and compares it to Glass‐FRP composite. The study looked into the effect of number of layers on properties, comparing wet layup (WL) to vacuum bag (VB) molding, and aging in a 3.5% salt solution for up to 365 days at 23, 40, and 55°C. Results show that Flax‐FRP has a tensile strength and modulus of one third the values of Glass‐FRP. Using the VB process, Flax‐FRP showed a strength and modulus 18 and 36% higher, respectively, than WL specimens. As the number of layers increased from one to five, the strength and modulus also increased but stabilized at three layers. After 365 days of conditioning at 23, 40, and 55°C, WL specimens showed a strength retention of 81, 73, and 69%, respectively. Using the Arrhenius relationship, it was estimated that both WL and VB Flax‐FRP would retain 60% of their tensile strength after 100 years of saltwater exposure at an annual mean temperature of 10°C. POLYM. COMPOS., 37:3234–3244, 2016. © 2015 Society of Plastics Engineers