Adsorption studies of Cr(III) ions from aqueous solutions by DEHPA impregnated onto Amberlite XAD7 – Factorial design analysis

The present paper investigates the adsorption of Cr(III) ions using the SIR, prepared by impregnation of Amberlite XAD7 with di-(2-ethylhexyl)-phosphoric acid (DEHPA), which has been chosen as an extractant for the purpose of this study. The Amberlite XAD7–DEHPA resin was impregnated with DEHPA and ethylic alcohol as solvent trough dynamic column impregnation method. The influence of different physicochemical parameters (pH, resin dosage, initial concentration of Cr(III) ions, contact time and temperature) upon the adsorption capacity of XAD7–DEHPA, in the Cr(III) ions removal process from aqueous solution, has been investigated. The pH for Cr(III) ions adsorption was found as 3.0 for this material. The results showed that the adsorption equilibrium was reached after 45 min. The adsorption process is best described by the pseudo-second order kinetic model. Langmuir adsorption isotherm gave a satisfactory fit of the equilibrium data. The maximum adsorption capacity is ∼3 mg Cr(III) ions/g SIR. The thermodynamic studies allowed us to determine the thermodynamic parameters ΔG°, ΔH° and ΔS°. In this paper the factorial design of experiments was used to study the performance of the adsorption process.     

Design of an Auger-Suppressed Unipolar HgCdTe NBνN Photodetector

A unipolar mercury cadmium telluride (HgCdTe) NBνN infrared (IR) device architecture is analyzed by physics-based numerical device simulations. The device structure is predicted to suppress Shockley–Read–Hall (SRH) and Auger generation–recombination (G–R) processes, while also providing a simplified fabrication process by eliminating p-type doping requirements. The performance characteristics of mid- and long-wavelength infrared (MWIR: λ _c?=?5?μm; LWIR: λ _c?=?12?μm) NBνN devices are calculated and compared with those of nBn and double-layer planar heterostructure (DLPH) devices. Theoretical dark current density (J _dark) values of the MWIR and LWIR NBνN devices are lower by an order of magnitude or more for temperatures between 50?K and 225?K. Calculated peak detectivity (D ^*) values of 6.01?× 10¹⁴?cm?Hz^0.5/W to 2.36?×?10¹⁰?cm?Hz^0.5/W for temperatures from 95?K to 225?K, and 2.37?×?10¹⁴?cm?Hz^0.5/W to 2.27?×?10¹¹?cm?Hz^0.5/W for temperatures from 50?K to 95?K are observed for MWIR and LWIR NBνN structures, respectively. A component of the NBνN structure, embodied in a unipolar MWIR nBn device, is also fabricated to experimentally demonstrate selective carrier extraction.     

Sinanodonta woodiana (mollusca: bivalvia: unionidae): isolation and characterization of the first microsatellite markers

Sinanodonta woodiana (Lea, 1834) is a large Unionid species with a real invasion success. It colonized Europe, Central America, the Indonesian Islands and recently North America. The species life cycle involves a larval parasitic stage on freshwater fish species which contributes to the spread of the mussel. In this paper we describe, for the first time, eight polymorphic microsatellite loci for the species Sinanodonta woodiana. The genetic screening of individuals confirmed that all loci were highly polymorphic. The number of alleles per locus ranged from 7 to 14 and the observed heterozygosity ranged from 0.650 to 0.950. These loci should prove useful to study the species population genetics which could help to infer important aspects of the invasion process.     

Structural Analysis,Electrochemical Behavior,and Biocompatibility of Novel Quaternary Titanium Alloy with near β Structure

This article analyses the microstructure, electrochemical behavior, and biocompatibility of a novel Ti-20Nb-10Zr-5Ta alloy with low Young’s modulus (59 GPa) much closer to that of bone, between 10 and 30 GPa, than Ti and other Ti alloys used as implant biomaterial. XRD and SEM measurements revealed a near β crystalline microstructure containing β phase matrix and secondary α phase, with a typical grain size of around 200 μm. The corrosion behavior in neutral Ringer solution evidenced: self-passivation behavior characterizing a very resistant passive film; an easy passivation as a result of favorable influence of the alloying elements Nb, Zr, and Ta that participate with their passive oxides to the formation of the alloy passive film; low corrosion and ion release rates corresponding with very low toxicity. In MEM solution, the novel alloy demonstrated very high corrosion resistance and no susceptibility to localized corrosion. Biocompatibility was evaluated on in vitro human osteoblast-like and human immortalized pulmonary fibroblast cell (Wi-38) lines and the new Ti-20Nb-10Zr-5Ta alloy exhibited no cytotoxicity. The new Ti-20Nb-10Zr5Ta alloy is a promising material for implants due to combined properties of low elastic modulus, very low corrosion rate, and good biocompatibility.     

Influence of the Carbo-Chromization Process on the Microstructural,Hardness, and Corrosion Properties of 316L Sintered Stainless Steel

We report on the changes on the microstructural, hardness, and corrosion properties induced by carbo-chromization of 316L stainless steel prepared by Spark Plasma Sintering technique. The thermo-chemical treatments have been performed using pack cementation. The carburizing and chromization were carried out between 1153 K (880 °C)/4 h to 1253 K (980 °C)/12 h and 1223 K (950 °C)/6 h to 1273 K (1000 °C)/12 h in a solid powder mixture of charcoal/BaCO₃ and ferrochromium/alumina/NH₄Cl, respectively. The obtained layers were investigated using X-ray and electron diffraction, optical and scanning electron microscopies, Vickers micro-hardness, and potentiodynamic measurements. The thickness of the carbo-chromized layer ranges between 300 and 500 μm. Besides the host γ-phase, the layers are mainly constituted of carbides (Fe₇C₃, Cr₂₃C₆, Cr₇C₃, and Fe₃C) and traces of α′-martensite. The average hardness values decrease smoothly from 650 HV at the sample surface down to 200 HV at the center of the sample. The potentiodynamic tests revealed that the carbo-chromized samples have smaller corrosion resistance with respect to the untreated material. For strong chromization regimes, the corrosion rate is increased by a factor of four with respect to that of the untreated material, while the micro-hardness of the layer is three times larger. Such materials are suited to be used in environments where good corrosion resistance and wear properties are required.     

Diffusional System Based on Tolazoline Hydrochloride Included in a Reticulated Carboxymethylcellulose Hydrogel

This paper presents a diffusional system consisting of tolazoline hydrochloride included into a carboxymethylcellulose based hydrogel, showing a high swelling capacity in water. The process kinetics of the drug inclusion into hydrogel as well as of the drug releasing have been studied. The tolazoline hydrochloride release was performed by elution with a simulated biological fluid within the digestive tract, at the small intestine level (pH = 8.2) where the drug is mostly absorbed. The results make evident a zero-order kinetics over the 30–400 min range, which would place the system among those with ‘sustained’ release, with obvious advantages compared with the classical drug administration.     

An experimental study of a confined and submerged impinging jet heat transfer using Al2O3-water nanofluid

An experimental investigation was performed to study the heat transfer performance of a 36 nm-Al₂O₃-particle–water nanofluid in a confined and submerged impinging jet on a flat, horizontal and circular heated surface. The tests were realized for the following ranges of the governing parameters: the nozzle diameter is 3 mm and the distance nozzle-to-heated-surface was set to 2, 5 and 10 mm; the flow Reynolds number varies from 3800 to 88 000, the Prandtl number from 5 to 10, and the particle volume fraction is ranging from 0 to 6%. Experimental data, obtained for both laminar and turbulent flow regimes, have clearly shown that, depending upon the combination of nozzle-to-heated surface distance and particle volume fraction, the use of a nanofluid can provide a heat transfer enhancement in some cases; conversely, for other combinations, an adverse effect on the convective heat transfer coefficient may occur. Within the experimental parameters used, it has been observed that highest surface heat transfer coefficients can be achieved using an intermediate nozzle-to-surface distance of 5 mm and a 2.8% particle volume fraction nanofluid. Nanofluids with high particle volume fractions, say 6% or higher, have been found not appropriate for the heat transfer enhancement purpose under the confined impinging jet configuration. On the other hand, for a very small and a large distance of nozzle-to-heated-surface, it has been observed that the nanofluid use does not provide a perceptible heat transfer enhancement and has, for some particular cases, produced a clear decrease of the convective heat transfer coefficient while compared to that obtained using distilled water.     

On heat transfer in external natural convection flows using two nanofluids

In the present work, a theoretical model based on the integral formalism approach for both laminar and turbulent external natural convection is extended to nanofluids. By using empirical models based on experimental data for computing viscosity and thermal conductivity of water–alumina and water–CuO suspensions, a close attention is first focused on the influence due to increasing the volume fraction of nanoparticles on the heat transfer and then to the transition threshold between laminar and turbulent regimes. The heat transfer is shown to strongly depend on the flow regime and on particle volume fraction. A clear degradation of heat transfer is observed using nanofluids while compared to that of the base-fluid. Moreover, the fact of increasing the particle volume fraction tends to delay the occurrence of the flow transition to turbulence.     

Poly(2-hydroxyethyl methacrylate-co-dodecyl methacrylate-co-acrylic acid): synthesis,physico-chemical characterisation and nafcillin carrier

In the present study polymeric microbeads of poly(2-hydroxyethyl methacrylate-co-dodecyl methacrylate-co-acrylic acid) or p(HEMA-co-dDMA-co-AA) were synthesised and characterized through FT-IR and scanning electron microscopy (SEM); their swelling behavior against saline solution was explored and their in vitro cytotoxicity was evaluated. Further, in order to elucidate kinetic aspects regarding the ternary system p(HEMA-co-dDMA-co-AA), a mathematical model of the reactivity ratios of the comonomers in the terpolymer has been conceived and analyzed. An intensified tendency of AA units accumulation in the copolymer has been noticed, in spite of HEMA units, while dDMA conserves in the copolymer the fraction from the feed. Three compositions have been selected for nafcillin-loading and their in vitro release capacity was evaluated. The compositions of 80:10:10 and 75:10:15 M ratios appear suitable for further in vivo testing, in order to be used as drug delivery systems in the treatment of different osseous diseases.     

Porous microparticles based on methacrylic copolymers and gellan as drug delivery systems

Two types of porous microparticles based on glycidyl methacrylate, dimethacrylic monomers (ethylene glycol dimethacrylate, diethylene glycol dimethacrylate and triethylene glycol dimethacrylate) and gellan were prepared by two methods. The first method was aqueous suspension polymerization in the presence of N‐butyl acetate as porogenic agent when the crosslinking and grafting reactions were achieved in a single step. The second method was based on the reaction between hydroxyl groups belonging to gellan and the epoxy groups situated on the surface of porous microparticles based on glycidyl methacrylate and dimethacrylic monomers in basic medium. The microparticles with and without gellan were characterized by Fourier transform infrared spectroscopy, SEM, AFM and TGA. Also, the porous structure was investigated in terms of pore volume, porosity and specific surface. The swelling behaviour in aqueous solution with different pH values as well as sorption studies of cefuroxime sodium salt onto porous microparticles were investigated. The presence of gellan in the structure of the microparticles leads to porous materials characterized by higher specific surface areas (S_sp = 78–140 m² g^–1), higher swelling capacities (S_w = 162%–365%) and higher sorption capacities of the drug (q_e = 101–147 mg g^–1) compared to microparticles without gellan in their structures (S_sp = 73–85 m² g^–1; S_w = 139%–209%; q_e = 70–110 mg g^–1). © 2019 Society of Chemical Industry