Evaluation of functional,antinutritional, pasting and microstructural properties of Millet flours

In the present study finger and pearl millet grains were milled and sieved to obtain flour. The flours were evaluated for chemical composition, nutritional, antinutritional, pasting and micro structural properties. Significant difference (p < 0.05) in nutrient and antinutrient contents was found among the millet flours. Protein, ash and fiber content of millet flours vary from 7.3 to 8.0 g/100 g, 2.73 to 5.16 g/100 g and 3.03 to 3.05 g/100 g. Results obtained for antinutrient factors in finger and pearl millet flours were (3.5 mg/g) and (2.2 mg/g) for tannic acid and (6.1 mg/g) and (9.2 mg/g) for phytic acid respectively. Mineral availability of pearl and finger millet flour (mg/100 g) was (109.2–139.2), (0.73–4.2), (1.18–8.7.0), (15.03–17.36) and (67.53–30.03) for calcium, zinc, iron, sodium and potassium respectively. Finger millet flour showed higher peak viscosity, breakdown, final and set back value compared to pearl millet flour. Findings from the scanning electron microscopy analysis showed microstructural differences in both millet flours. FTIR analysis showed that both finger and pearl millet flours possessed O–H and C–H compounds.     

Comparative sequence analysis of spa gene of Staphylococcus aureus isolated from bovine mastitis: characterization of an unusual spa gene variant

The protein A encoding gene spa of four Staphylococcus aureus strains isolated from bovine clinical mastitis was amplified by PCR and sequenced. The four strains were selected after an initial screening of spa gene of 41 strains isolated from mastitic cows and were subjected to detailed investigations. According to the sequencing results the spa gene of three strains (M1, M2, M3) appeared with gene segments encoding five (E, D, A, B and C) and four (E, A, B and C) IgG binding domains for two (M1, M3) and one (M2) strain, respectively and with gene segments encoding four, two and two repeats of the octapeptide Xr-repeats for the strains M1, M2 and M3, respectively. For the remaining Staph. aureus strain (M4) gene segments encoding IgG binding domains E, D and A and a new domain BC with a size of 219 bp could be observed. The BC domain appears, with a deletion of a 123 bp segment from the border region between both domains, as fused domain of both previously characterized domains. The Xr-region of this strain had 11 octapeptide repeats.     

Physico-chemical properties of various palm-based diacylglycerol oils in comparison with their corresponding palm-based oils

Palm-based diacylglycerol (P-DAG) oils were produced through enzymatic glycerolysis of palm kernel oil (PKO), palm oil (PO), palm olein (POL), palm mid fraction (PMF) and palm stearin (PS). High purity DAG (83–90%, w/w) was obtained and compared to palm-based oils (P-oil) had significantly (P < 0.05) different fatty acid composition (FAC), iodine value (IV) and slip melting point (SMP). Solid fat content (SFC) profiles of P-DAG oils as compared to P-oils had less steep curves with lower SFC at low temperature range (5–10 °C) and the higher complete melting temperatures. Also, P-DAG oils in contrast with P-oils showed endothermic as well as exothermic peaks with higher transition temperatures and significantly (P < 0.05) higher crystallisation onsets, heats of fusion, and heats of crystallisation. Crystal forms for P-DAG oils were mostly in the β form.     

Thermotropic phase properties of the hydroxyceramide/cholesterol system

The interaction of cholesterol with ceramides containing α-hydroxy fatty acyl chains (hydroxyceramides) has been studies as a foundation for characterizing the lipid bilayers of thestratum corneum. A relatively large quantity of cerebrosides was obtained from bovine brain and converted to ceramides through removal of the carbohydrate side chain. The ceramides were separated based on the absence or presence of hydroxy fatty acyl chains. The lyophilized hydroxyceramides showed a broad melting region at 92°C. Hydroxyceramides dispersed in water produced a relatively narrow, thermotropic transition at 75°C. The effect of cholesterol on this thermotropic phase transition of hydroxyceramides was determined by differential scanning calorimetry. With respect to the main transition, cholesterol caused a broadening of the phase transition at relatively low levels as well as a decrease in the peak transition temperature. The presence of cholesterol at levels in excess of 7 wt% gave rise to an additional low-temperature transition at 55°C. Upon immediate rescanning, this transition was exothermic, but with increasing incubation time the area under the excess heat capacity curve as a function of temperature became smaller. After two days or more, the transition observed was endothermic. At cholesterol levels between 40 and 50 wt%, multiple peaks were observed. From comparisons with related systems, the cooperative thermal transitions of hydroxyceramides with cholesterol are suggested to result from changes in hydrogen bonding or be due to phase separation. The composition of isolated brain ceramides is being compared with that reported for thestratum corneum.     

Fabrication of self-ordered nanoporous alumina with 500–750 nm interpore distances using hard anodization in phosphoric/oxalic acid mixtures

A hard anodization (HA) technique is employed using different mixtures of phosphoric/oxalic acid for fast fabrication of alumina nanopore arrays in voltages higher than 200 V. The mixtures enable to avoid the breakdown of porous anodic alumina (PAA) in the high voltages. It is revealed for the first time that continuously tunable pore intervals (D_int) from 500 to 750 nm can be controlled by varying the concentrations of oxalic acid at anodization voltages (U_anod) from 230 to 360 V, far beyond the U_anod in the single electrolyte of phosphoric acid or oxalic acid. The ratios of interpore distance, pore diameter and barrier layer thickness to anodization voltage are in the range of conventional HA process for each acid mixture. In this approach, the PAA film growth rate is 26 µm/h, being 7 times larger than that in typical mild anodization.     

Study on morphology,thermal, mechanical and Cd(II) adsorption properties of PVC/α-MnO<Subscript>2</Subscript>-stearic acid nanocomposites: production and application

Alpha manganese dioxide nanorods (α-MnO₂) were successfully functionalized with stearic acid (SA) by solvothermal method to prevent agglomeration. The α-MnO₂-SA nanorods were employed as a filler for the preparation of poly(vinyl chloride) (PVC) nanocomposite (NC) films with different percentages (1, 3 and 5 wt%). The morphology, mechanical and thermal properties of the obtained NCs were investigated. The results showed that α-MnO₂-SA can effectively improve the properties of PVC. The enhancement in properties of the NCs was attributed to the improved interfacial bonding by modification. Also, these NCs were used as adsorbent for removal of cadmium ions. Our finding suggests that the PVC/α-MnO₂-SA NCs are good candidates for efficient Cd(??) removal from the wastewater.     

Synthesis of Vanadium Pentoxide Nanoparticles as Catalysts for the Ozonation of Palm Oil

Vanadium pentoxide nanoparticles were synthesized using a solvo-thermal method and were characterized via X-ray powder diffraction (XRD) and field emission scanning electron microscopy (FE-SEM). The ozonation of palm oil was performed by using vanadium pentoxide nanoparticles as catalysts to synthesize ethyl malonate. This procedure presented several advantages, such as simple operation for a precise ozonation, excellent yield, short reaction times and reusability because of the recyclability of palm oil. Ethyl malonate was synthesized via the one-step ozonolysis of palm oil and was spectroscopically characterized using gas chromatography-mass spectroscopy (GC-MS).     

Generation of monodisperse aerosols by combining aerodynamic flow-focusing and mechanical perturbation

A novel instrument has been developed for generating highly monodisperse aerosol particles with a geometrical standard deviation of 1.05 or less. This aerosol generator applies a periodic mechanical excitation to a micro-liquid jet obtained by aerodynamic flow-focusing. The jet diameter and its fastest growth wavelength have been optimized as a function of the flow-focusing pressure drop and the liquid flow rate. The monodisperse aerosol generated by this instrument is also charge neutralized with bipolar ions produced by a non-radioactive, corona discharge device. Monodisperse droplet generation in the 15- to 72-μm diameter range from a single 100-micron nozzle has been demonstrated. Both liquid and solid monodisperse particles can be generated from 0.7- to 15-μm diameter by varying solution concentration, liquid flow rate, and excitation frequency. The calculated monodisperse particle diameter agrees well with independent measurements. The operation of this new monodisperse aerosol generator is stable and reliable without nozzle clogging, typical of other aerosol generators at the lower end of the operating particle size ranges.

Copyright © 2016 American Association for Aerosol Research     

Photo-induced superhydrophilicity of nanocomposite TiO2-SiO2 thin film

In this work, TiO₂ and TiO₂-SiO₂ thin films on glass substrates were prepared by the sol-gel dip coating process. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) were used to evaluate the structural and chemical properties of the films. The super-hydrophilicity was assessed by water contact angle measurement. XRD measurements confirmed the presence of polycrystalline anatase and rutile phases in the films. The water contact angle measurements showed that addition of SiO₂ has a significant effect on the super-hydrophilicity of TiO₂ thin films, especially if they are stored in a dark place.     

Removal of CO from process gas with Sn–activated carbon in pressure swing adsorption

A pressure swing adsorption (PSA) system using activated carbon impregnated with SnCl ₂·2H ₂ O and pure activated carbon was used to remove CO from a model H ₂/CO mixture representing the steam reformer process gas. On comparing PSA results for both carbons, the CO adsorptive capacity of impregnated carbon was found to be superior to that of the pure carbon. This was confirmed by the fact that the concentration of CO, initially at 1000 ppm, was successfully reduced to 4.02% and 1.04% of its initial concentration by the pure and the impregnated activated carbons respectively in the PSA system. The species in the impregnated carbon responsible for the improved gas phase CO adsorption was found to be SnO ₂. Simulation results at a cyclic time of 600 s in the PSA operating at 10 atmospheres gave a product recovery and purity of 99.99% and 57.48%, respectively. At 6 atmospheres, the product recovery and purity were 92.17% and 77.12%, respectively. © 2000 Society of Chemical Industry