Microbial corrosion of Ni–Cu alloys by Aeromonas eucrenophila bacterium

The corrosion behavior of Ni–Cu alloy in Nutrient Broth medium (peptone from meat 5.0 g, meat extract (N source) 3.0 g, and sodium chloride 6.0 g in 1 L) and in the presence of Aeromonas eucrenophila, isolated from water treatment system, has been studied using electrochemical techniques. Results showed that the polarization curves exhibiting a cathodic shift of the corrosion potential confirmed the increase in the corrosion rates. According to EIS data lower Q_CPE value for 5 h indicates surface inhomogeneity resulting from surface metal roughening, which is the likely cause of the enhanced dissolution of the metal also observed in SEM micrographs. In addition, the pH values of the medium did not change throughout the experiment; however, after immersion the pH value decreased to acidic value and caused corrosion.     

ELECTRO-DEIONIZATION OF Cr (VI)-CONTAINING SOLUTION. PART I: CHROMIUM TRANSPORT THROUGH GRANULATED INORGANIC ION-EXCHANGER

Kinetics of Cr (VI) → OH^? exchange on both hydrogel and xerogel of hydrated zirconium dioxide was investigated. Self-diffusion coefficient of Cr (VI) species has been determined by analysis of kinetic curves. Transport of Cr (VI) anions through the inorganic ion exchangers under the influence of applied voltage was also researched. In the case of hydrogel, the ions are transported mainly through the solid phase. Diffusion coefficient of chromate anions through this material was estimated as 9.00 × 10^?12 m² s^?1. This is in agreement with self-diffusion coefficient of Cr (VI) obtained from kinetic measurements (1.60 × 10^?12–9.92 × 10^?12 m² s^?1). Owing to the rather high mobility of Cr (VI) through hydrogel of hydrated zirconium dioxide, this material was recommended for electro-deionization processes. On the other hand, the use of polymer anion-exchange membrane must be excluded to prevent poisoning of the inorganic ion exchanger with Cr (III) cations to be formed during chemical interaction of Cr (VI) with organic materials.     

Investigation of the sensory properties of the flesh of rainbow trout (Oncorhynchus mykiss) fed diets with astaxanthin, shrimp waste meal and red pepper meal

Sensory properties (colour, general appearance and taste) were investigated in rainbow trout, Oncorhynchus mykiss, fed standard diets supplemented with either 60 mg/kg astaxanthin, shrimp waste meal or red pepper meal. The fish were divided into three experimental groups (fed diets supplemented with pigments) and one control group, and fed experimental and control diets for 100 days. After the feeding period, the fish were evaluated for sensory properties. Colour was evaluated using a colour card for salmonids. General appearance and taste were evaluated using hedonic scaling. Significant differences between the fish fed diets with and without pigment supplementation were found. Feeding of rainbow trout with diets supplemented with pigments affected their sensory properties.     

Solvent-impregnated resins (SIRs) – Methods of preparation and their applications

Interest in the development of solvent-impregnated resins (SIRs) and their applications for the separation of metal ions and organic compounds from water in the form of a hybrid polymeric adsorbent material has intensified over the past thirty years. SIRs are particulate adsorbers that possess a combination of the advantageous features of both liquid–liquid extraction and ion exchange and this renders them applicable to a wide range of potential liquid–solid separation and recovery processes. This paper reviews the extensive published literature on methods of synthesis of SIRs, attempts to stabilize hybrid solvent-impregnated resins and various applications of SIRs.     

Biosorption of chromium(VI), nickel(II) and Remazol blue by Rhodotorula muciloginosa biomass

The passive removal of commonly used reactive dye and two heavy metals, from aqueous solutions by inexpensive biomaterial, yeast Rhodotorula muciloginosa biomass, termed biosorption, was studied with respect to pH, initial dye concentration and initial metal ion concentration. The biomass exhibited maximum dye and chromium(VI) uptake at pH 5 and pH 6 for nickel(II) in media containing 50 mg/L heavy metal and 50 mg/L remazol blue. It was found that the highest chromium(VI) removal yields measured were 31.3% for 49.0 mg/l initial chromium(VI) concentrations. The nickel(II) removal yield was 32.5% for 22.3 mg/L. Higher R. Blue removal yields were obtained, such as 77.1% for 117.5 mg/L. The maximum dye biosorption yield was investigated in medium with a constant dye (approximately 50 mg/L) and increasing heavy metal concentration. In the medium with 48.8, 103.8 and 151.8 mg/L chromium(VI) and constant dye concentration, the maximum chromium(VI) biosorption was 7.4, 9.3 and 17.1%, whereas the maximum dye biosorption was 61.6, 56.6 and 55.9%. The maximum nickel(II) biosorptions in the medium with dye were 38.1, 22.1 and 8.8% at 23.7, 37.7 and 60.1 mg/L nickel(II) concentrations. In these media, dye biosorptions were 93.9, 86.4 and 93.3%, respectively.     

Porous dye affinity beads for albumin separation from human plasma

Porous polymeric beads were obtained by the suspension polymerization of 2‐hydroxyethyl methacrylate (HEMA) and ethylene glycol dimethacrylate (EGDMA). Poly(HEMA–EGDMA) beads were characterized by surfacearea measurements, swelling studies, FTIR, scanning electron microscopy (SEM), and elemental analysis. Poly (HEMA–EGDMA) beads had a specific surface area of 56 m²/g. SEM observations showed that the poly(HEMA–EGDMA) beads abounded macropores. Poly(HEMA–EGDMA) beads with a swelling ratio of 55%, and containing different amounts of Reactive Red 120 (9.2–39.8 μmol/g) were used in the adsorption/desorption of human serum albumin (HSA) from aqueous solutions and human plasma. The nonspecific adsorption of HSA was very low (0.2 mg/g). The maximum HSA adsorption amount from aqueous solution in phosphate buffer was 60.1 mg/g at pH 5.0. Higher HSA adsorption value was obtained from human plasma (up to 95.7 mg/g) with a purity of 88%. The equilibrium monolayer adsorption amount, Q_max was determined as 172.4 mg/g. The dimensionless separation factor (R_L) value shows that the adsorption behavior of HSA onto the Reactive Red 120 attached poly(HEMA–EGDMA) beads was favorable (0 < R_L < 1). Desorption of HSA from Reactive Red 120 attached poly (HEMA–EGDMA) beads was performed using 0.1M Tris/HCl buffer containing 0.5M NaCl. It was observed that HSA could be repeatedly adsorbed and desorbed with Reactive Red 120‐attached poly(HEMA–EGDMA) beads without significant loss in the adsorption amount. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Trace elements in edible tissues of three shrimp species (Penaeus semisulcatus,Parapenaeus longirostris and Paleomon serratus)

Accumulation levels of trace elements in edible tissues of three shrimp species (Penaeus semisulcatus, Parapenaeus longirostris and Paleomon serratus) from the Gulf of Antalya, Turkey were investigated. Copper (Cu), cadmium (Cd), zinc (Zn), iron (Fe) and manganese (Mn) concentrations were determined by atomic absorption spectrophotometry. The lowest Cu (1.33 mg kg^?1) and Cd (0.23 mg kg^?1) and highest Mn (1.52 mg kg^?1) concentrations were found in P. longirostris, the lowest Zn (6.25 mg kg^?1), Fe (1.84 mg kg^?1) and Mn (0.25 mg kg^?1) concentrations in P. serratus and the highest Cu (6.19 mg kg^?1), Cd (2.36 mg kg^?1), Zn (30.84 mg kg^?1) and Fe (33.89 mg kg^?1) concentrations in P. semisulcatus. The Cd levels detected in P. semisulcatus and P. serratus were above legislative limits. Our results show that there were significant differences in trace element concentrations among the three shrimp species. The highest levels of the five trace elements investigated, with the exception of Mn, were found in edible tissue of P. semisulcatus. Copyright © 2007 Society of Chemical Industry     

Synthesis of polydimethylsiloxane‐block‐polystyrene‐block‐polydimethylsiloxane via polysiloxane‐based macroinitiator in supercritical CO2

Polydimethylsiloxane‐block‐polystyrene‐block‐polydimethylsiloxane (PDMS‐b‐PS‐b‐PDMS) was synthesized by the radical polymerization of styrene using a polydimethylsiloxane‐based macroazoinitiator (PDMS MAI) in supercritical CO₂. PDMS MAI was synthesized by reacting hydroxy‐terminated PDMS and 4,4′‐azobis(4‐cyanopentanoyl chloride) (ACPC) having a thermodegradable azo‐linkage at room temperature. The polymerization of styrene initiated by PDMS MAI was investigated in a batch system using supercritical CO₂ as the reaction medium. PDMS MAI was found to behave as a polyazoinitiator for radical block copolymerization of styrene, but not as a surfactant. The response surface methodology was used to design the experiments. The parameters used were pressure, temperature, PDMS MAI concentration and reaction time. These parameters were investigated at three levels (?1, 0 and 1). The dependent variable was taken as the polymerization yield of styrene. PDMS MAI and PDMS‐b‐PS‐b‐PDMS copolymers obtained were characterized by proton nuclear magnetic resonance and infrared spectroscopy. The number‐ and weight‐average molecular weights of block copolymers were determined by gel permeation chromatography. Copyright © 2004 Society of Chemical Industry     

Synthesis and in vitro antimicrobial characterization of Boron-PVA Electrospun nanofibers

Polyvinyl alcohol (PVA) electrospun nanofibers and boric acid (BA) complexes of these nanofibers were synthesized with and without using TritonX-100(TX-100) as a water soluble surfactant (PVA, PVA/BA, PVA/TX-100, PVA/TX-100/BA). The electrospun nanofibers were characterized by SEM, FTIR and TGA. Preliminary results showed that certain amount of boric acid decreased the number of Stapylococcus aureus from 6,8x10⁷(CFU/mL) to 3x10⁷(CFU/mL). In the preparation of polymer, boric acid was used as a crosslinker and antimicrobial agent whereas TX-100 was used as surfactant. The viscosity and conductivity measurements indicated that the BA increased viscosity but decreased conductivity. In contrast, TX-100 increased conductivity without considerable effect on viscosity, which affects the production and resulting nanofiber properties such as diameter and bead formation. The antimicrobial activities of the nanofibers were assayed in vitro by Gram-negative (E. coli) and Gram-positive(S. aureus) bacteria. It was observed that PVA/TX-100/BA showed better antibacterial activity against S.aureus bacteria compared to PVA and PVA/TX-100 nanofibers.