Mathematical modeling of reverse osmosis systems

The present investigation pertains to modeling of seawater desalination system. A simulation model was developed and verified for a small-scale reverse osmosis system. The proposed model combines material balances on the feed tank, membrane module andproduct tank with membrane mass transfer models. Finally a comprehensive simulation model has been developed incorporating the effect of mass transfer inhibition The model is non-linear differential equation representing the feed concentration as a function of operating time and space. The solution of the simultaneous differential equations was obtained using the fourth order Runge-Kutta method, due to self starting and stability. The model was verified using the experimental data from the literature [17,24]. Parameter sensitivity was carried out to select the proper step size. The simulation was run for over 1000 11 enabling a prediction of operational performance at high overall system recoveries.     

Study on the structure and properties of nanocomposites based on high-density polyethylene/starch blends

The effects of nanoclay on the structure and final properties of high density polyethylene (HDPE)/thermoplastic starch (TPS) blends were investigated. Neat blends as well as nanoclay containing samples were prepared by melt blending in an internal mixer. Also, a poly (ethylene-g-maleic anhydride) (PE-g-MA) copolymer was used as compatibilizer in some of the formulations. Nanocomposites with intercalated structures were obtained in the samples lacking the compatibilizer, based on the rheological, X-ray diffraction (XRD) and transmission electron microscopy (TEM) results. However, some of the silicate layers were nearly exfoliated in the presence of the compatibilizer. The nanoclay was located preferably in the HDPE matrix as well as at the interface of the HDPE matrix and TPS dispersed phase. The ability of the nanoclays in decreasing the average size of TPS phase in the HDPE matrix was confirmed by scanning electron microscopy (SEM) observations. Furthermore, thermo-gravimetric analysis (TGA) showed that the nanoclays could enhance the thermal stability of the samples. It seems that nanoclays performed as an insulator and mass transport barrier to the small molecules generated during decomposition, and assisted in the formation of char after thermal decomposition of the polymer matrix. All the samples containing the compatibilizer possessed higher tensile strength and elongation at break, but lower modulus, compared to the corresponding un-compatibilized samples. Finally, incorporation of the nanoclays was found to be in favor of developing nanocomposites with higher biodegradability as evidenced through a biodegradation test by fungi as well as water uptake experiments.     

Development of a fluidized bed thermogravimetric analyzer

A new fluidized bed thermogravimetric analyzer (FB‐TGA) was developed that introduces two major particularities: the pseudo variation of the weight of the reactor and the special strategy for gas flow rate adjustment according to temperature. A momentum balance was performed on the reactor and the pseudo variation of the reactor weight was evaluated by measuring the pressure drop through the gas distributor and filter. The real weight loss of the reactor was obtained by subtracting the pseudo variation of the weight from the total weight loss measured by the load cell. In addition, a special program for the gas flow rate as a function of temperature was developed and used; so the minimum fluidization regime is maintained throughout all of the experiments. The validation test of the FB‐TGA was carried out on calcium hydroxide decomposition, and the results were compared with those obtained from the conventional TGA. Diffusion control was suppressed by the application of the FB‐TGA, which was confirmed by the x‐ray diffraction analysis on the treated samples. © 2014 American Institute of Chemical Engineers AIChE J, 61: 84–89, 2015     

Nanomechanical and tribological behavior of hydroxyapatite reinforced ultrahigh molecular weight polyethylene nanocomposites for biomedical applications

A hydroxyapatite (HA) particulate reinforced ultrahigh molecular weight polyethylene (UHMWPE) nanocomposite is fabricated by internal mixer at 180°C and using of paraffin oil as a processing aid to overcome the high viscosity of melted UHMWPE. The reinforcing effects of nano‐HA are investigated on nanomechanical properties of HA/UHMWPE nanocomposites by nanoindentation and nanoscratching methods. Results show that the nanocomposite with 50 wt % nano‐HA exhibits a Young's modulus and hardness of 362.5% and 200% higher, and a friction coefficient of 38.86% lower than that of pure UHMWPE, respectively. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42052.     

Radical polymerization of methyl methacrylate (MMA) initiated by KHSO5 – BTBAC system - a kinetic study

Kinetics of free radical polymerization of methyl methacrylate using potassium peroxomonosulfate as initiator in the presence of benzyltributylammonium chloride (BTBAC) as phase transfer catalyst was studied. The polymerization reactions were carried out under nitrogen atmosphere and unstirred conditions at a constant temperature of 60°C in ethyl acetate/water bi-phase system. The role of concentrations of monomer, initiator, catalyst, temperature, acid and ionic strength on the rate of polymerization (R_p) was ascertained. The orders with respect to monomer, initiator and phase transfer catalyst were found to be 1.5, 0.5 and 0.5 respectively. The rate of polymerization (R_p) is independent of ionic strength and pH. Based on the kinetic results, a suitable mechanism is proposed.     

Synthesis of A<Subscript>2</Subscript>B<Subscript>2</Subscript> miktoarm star copolymers from a new heterobifunctional initiator by combination of ROP and ATRP

Abstract  

A new heterobifunctional initiator, 2,3-bis(2-bromo-2-methylpropionyloxy) succinic acid, was synthesized and used in preparation of A₂B₂ miktoarm star copolymers, (polystyrene)₂(poly(ε-caprolactone))₂, by combination of atom transfer radical polymerization (ATRP) and Controlled ring-opening polymerization (ROP). The structures of products were confirmed by the ¹H NMR, ¹³C NMR, FT–IR, elemental analysis, differential scanning calorimetry (DSC), and gel permeation chromatography (GPC). GPC traces show that the obtained polymers have a relatively narrow molecular weight distribution. The compositions of resulting miktoarm star copolymers were very close to theoretical.     

High dielectric permittivity and percolative behavior of polyvinyl alcohol/potassium dihydrogen phosphate composites

A new kind of anhydrous, transparent, and flexible potassium dihydrogen phosphate (KH₂PO₄ or KDP)/polyvinyl alcohol (PVA) composite in the form of film (0.10 mm) has been prepared by solution casting technique. KDP is well dispersed in the polymer matrix as observed from the microstructural studies. Frequency and temperature dependent dielectric properties of the composites have been studied with varying KDP concentrations. The PVA/KDP composite films exhibited extraordinarily high relative permittivity ε′ ∼ 430 (80 times higher compared with pure PVA and even higher than KDP) near the percolation threshold (ϕ_C = 2.5 wt % KDP) with low dielectric losses (∼ 0.15) at 1 kHz and room temperature. Such flexible, low loss and high dielectric permittivity material has enormous importance for application in devices. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Halloysite Nanotubes Modified by Fe3O4 Nanoparticles and Applied as a Natural and Efficient Nanocatalyst for the SymmetricalHantzsch Reaction

Halloysite as an impressive natural eco-friendly nanotube with aluminosilicate structure has been investigated recently due to its unique features such as specific morphology and excellent bio-adaptability. In this research, Fe₃O₄ nanoparticles have been loaded on the tubular halloysite by co-precipitation method in order to synthesis magnetic halloysite (Hal-Fe₃O₄₎. To characterize this recoverable nanocatalyst, applicable analyses such as Fourier-transform infrared (FT-IR) spectroscopy, energy-dispersive X-ray (EDX) analysis, field-emission scanning electron microscopy (FE-SEM) images, X-ray diffraction (XRD) pattern, Thermogravimetric analysis (TGA) and vibrating sample magnetometer (VSM) curves have been carried out. The results confirmed that Fe₃O₄ nanoparticles with cubic structure, and uniform distribution, were located at halloysite nanotubes (HNTs). This aluminosilicate nanocomposite with high thermal stability, crystalline structure, and stable morphology was evaluated as a heterogeneous catalyst in the symmetrical Hantzsch reaction for the first time. Easy synthesis process, green media, high performance, recoverable catalyst and reusing of the Hal-Fe₃O₄ as a nanocatalyst for 8 times are the main features of this protocol.

     

Decreasing the Sampling Time Interval in Radioactive Particle Tracking

The study of the movement of solids in multiphase reactors using radioactive particle tracking is currently limited to fairly modest particle velocities because of count‐rate limitations of the detection system. In this work, this restriction was overcome by increasing the activity of the radioactive tracer, by decreasing the sampling time interval and by modifying the particle tracking software to recognize which detectors were saturated and to use only the data from the remaining unsaturated detectors. Higher tracer activity resulted in lower standard deviation of the calculated tracer coordinates.     

Electrochemical investigations of pitting corrosion behaviour of type UNS S31603 stainless steel in thiosulfate-chloride environment

The pitting corrosion behaviour of type UNS S31603 stainless steel (316L SS) in 0.01, 0.05 and 0.1 M thiosulfate ion (S₂O₃ ^2–) in the absence and presence of various concentrations of chloride ion (Cl^–) was studied using the cyclic potentiodynamic polarization method. The influence of major factors which affect pitting corrosion such as pH and temperature, were also investigated. It was found that both the pitting potential (E _pit) and the repassivation potential (E _rp) decreased with increase in Cl^– concentration and solution temperature and a more pronounced difference in E _pit values for various concentrations of S₂O₃ ^2– in 1.0 M Cl^– was obtained at lower temperatures. The effect of pH on E _pit, E _corr and E _rp values for different concentrations of S₂O₃ ^2– in the presence of 1.0 M Cl^– was also determined.