Diffuse reflectance fourier transform infrared spectroscopy of phospholipid adsorption onto silicic acid

Diffuse reflectance Fourier transform infrared spectroscopy was used to study the mode of adsorption of phosphatidylcholine (PC) in hexane onto silicic acid (SA). PC adsorption was mainly through the charged phosphate group with minimal binding through the ester carbonyl. When the SA surface with adsorbed PC is washed with hexane, containing a small concentration of isopropanol, the desorbed PC is recovered without structural change, i.e., there is no evidence of PC hydrolysis in the adsorption process. Adsorbent misture probably promotes PC adsorption due to the increased availability of surface water hydroxyl groups for interaction with the PC phosphate groups. Isopropanol promoted PC binding by destabilizing PC reverse miscelles in solution, thus promoting its adsorption.     

Ultrahigh temperature water gas shift catalysts to increase hydrogen yield from biomass gasification

Noble metal (Rh, Pt, Pd, Ir, Ru, and Ag) and Ni catalysts supported on CeO₂–Al₂O₃ were investigated for water gas shift reaction at ultrahigh temperatures. Pt/CeO₂–Al₂O₃ and Ru/CeO₂–Al₂O₃ demonstrated as the best catalysts in terms of activity, hydrogen yield and hydrogen selectivity. At 700 °C and steam to CO ratio of 5.2:1, Pt/CeO₂–Al₂O₃ converted 76.3% of CO with 94.7% of hydrogen selectivity. At the same conditions, the activity and hydrogen selectivity for Ru/CeO₂–Al₂O₃ were 63.9% and 85.6%, respectively. Both catalysts showed a good stability over 9 h of continuous operation. However, both catalysts showed slight deactivation during the test period. The study revealed that Pt/CeO₂–Al₂O₃ and Ru/CeO₂–Al₂O₃ were excellent ultrahigh temperature water gas shift catalysts, which can be coupled with biomass gasification in a downstream reactor.     

Boron-doped hydrogenated amorphous carbon films grown by surface-wave mode microwave plasma chemical vapor deposition

We report the effects of boron (B) doping on optical and structural properties of the hydrogenated amorphous carbon thin films grown by surface-wave mode microwave plasma (SW-MWP) chemical vapor deposition (CVD) on n-type silicon and quartz substrates at room temperature. Argon and acetylene were used as a carrier and carbon source gases respectively. Analytical methods such as X-ray photoelectron spectroscopy (XPS), Nanopics 2100/NPX200 surface profiler, JASCO V-570 UV/VIS/NIR spectroscopy, Fourier transform infrared spectroscopy (FT-IR) and Raman spectroscopy were employed to investigate the properties of the films. Low atomic concentration of B (0.08 at.%) was found in the doped film. The optical band gap of the undoped film was 2.6 eV and it decreased to 1.9 eV for the B-doped film. Structural property shows the crystalline structure of the film and it has changed after incorporating B as a dopant. The structural modifications of the films leading to being more graphite in nature were confirmed by the Raman and FT-IR characterization.     

The role of pressure on thin amorphous carbon films deposited using microwave surface wave plasma CVD

We report the effects of gas composition pressure (GCP) on the optical, structural and electrical properties of thin amorphous carbon (a-C) films grown on p-type silicon and quartz substrates by microwave surface wave plasma chemical vapor deposition (MW SWP CVD). The films, deposited at various GCPs ranging from 50 to 110 Pa, were studied by UV/VIS/NIR spectroscopy, atomic force microscopy, Raman spectroscopy, X-ray photoelectron spectroscopy and current–voltage characteristics. The optical band gap of the a-C film was tailored to a relatively high range, 2.3–2.6 eV by manipulating GCPs from 50 to 110 Pa. Also, spin density strongly depended on the band gap of the a-C films. Raman spectra showed qualitative structured changes due to sp³/sp² carbon bonding network. The surfaces of the films are found to be very smooth and uniform (RMS roughness < 0.5 nm). The photovoltaic measurements under light illumination (AM 1.5, 100 mW/cm²) show that short-circuit current density, open-circuit voltage, fill factor and photo-conversion efficiency of the film deposited at 50 Pa were 6.4 μA/cm², 126 mV, 0.164 and 1.4 × 10^− 4% respectively.     

Curing characteristics and mechanical properties of alkali‐treated grass‐fiber‐filled natural rubber composites and effects of bonding agent

To improve adhesion between fiber and matrix, natural rubber was reinforced with a special type of alkali‐treated grass fiber (Cyperus Tegetum Rox b). The cure characteristics and mechanical properties of grass‐fiber‐filled natural rubber composites with different mesh sizes were studied with various fiber loadings. Increasing the amount of fibers resulted in the composites having reduced tensile strength but increased modulus. The better mechanical properties of the 400‐mesh grass‐fiber‐filled natural rubber composite showed that the rubber/fiber interface was improved by the addition of resorcinol formaldehyde latex (RFL) as bonding agent for this particular formulation. The optimum cure time decreased with increases in fiber loading, but there was no appreciable change in scorch time. Although the optimum cure time of vulcanizates having RFL‐treated fibers was higher than that of the other vulcanizates, it decreased with fiber loading in the presence of RFL as the bonding agent. But this value was lower than that of the rubber composite without RFL. Investigation of equilibrium swelling in a hydrocarbon solvent was also carried out. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 3151–3160, 2006     

Interphase of polyoctenamer-single-wall carbon nanotubes by thermogravimetric analysis in air

Non-isothermal thermogravimetric analysis in air, of polyoctenamer-single wall carbon nanotubes (PO-SWNTs), loaded by various amounts of SWNTs up to 10% wt., at different heating rates (ranging from 5 to 40°C/min) is reported. The thermal degradation in the air of PO_SWNTs is dominated by a main single sigmoidal dependence, assigned to the polymer and eventually polymer-nanofiller interphase, over which a weaker sigmoid assigned to the thermo-oxidative degradation of the nanofiller is superimposed at higher temperatures. The temperature at which the nanocomposite's residual mass fraction reaches x% wt. of the initial mass, T_x%, is reported (for x = 5, 50, and 85). The dependence of T_x% on the heating rate and the loading by nanotubes is analyzed. The temperature derivative of the thermograms defines new parameters (inflection residual mass fraction and inflection temperature) and (degradation) width. Their dependence on the loading by SWNTs was reported. Estimation of the interphase in polymer-based nanocomposites is based on the postulate that the dependence of the inflection temperature on the composition of the nanocomposite obeys a Fox-like dependence, where the bulk polymer and the polymer trapped within the interphase are considered as a blend of two miscible polymers. Complementary Raman, x-ray diffraction, and differential scanning calorimetry support these results.     

Short communication: Dairy bedding type affects survival of Prototheca in vitro

Protothecae are algal pathogens, capable of causing bovine mastitis, that are unresponsive to treatment; they are believed to have an environmental reservoir. The role of bedding management in control of protothecal mastitis has not been studied. The purpose of this study was to evaluate the growth of either environmental or mastitis-associated Prototheca genotypes in dairy bedding materials that are commonly used in Maine. Prototheca zopfii genotypes 1 and 2 (gt1 and gt2) were inoculated into sterile broth only (control ), kiln-dried spruce shavings, “green” hemlock sawdust, sand, or processed manure-pack beddings with broth, and incubated for 2 d. Fifty microliters of each isolate was then cultured onto plates and the resulting colonies counted at 24 and 48 h postinoculation. Shavings were associated with significantly less total Prototheca growth than other bedding types. Growth of P. zopfii gt1 was significantly higher than that of gt2 in the manure-pack bedding material. Spruce shavings, compared with manure, sand, or sawdust, may be a good bedding type to prevent growth of Prototheca. Based on these in vitro findings, bedding type may affect Prototheca infection of cattle in vivo.     

Copolymerization of lactic acid for cost-effective PLA synthesis and studies on its improved characteristics

The present study involves synthesis of polylactic acid (PLA) using purified lactic acid from fermented broth of Jackal jujube (Zizyphus oenophlia). A polyphenolic compound, humic acid (HA) of biological origin was incorporated to the PLA in order to reinforce the PLA chain without compromising its biodegradability and biocompatibility. Under optimized conditions of polymerization, modified L-PLA yield improved up to 93%. The molecular weight was found to be 6.4×10⁵. Different physicochemical properties of the polymer were explored for its further application in different fields. Incorporation of intermolecular bond between PLA and HA was confirmed by FT-IR spectroscopy technique. Addition of HA not only reduced the crystallinity of PLA, but also had increased flexibility and elasticity to much greater extent. The results showed that, apart from enhancing the physicochemical properties of PLA, the process also had reduced the production cost of the polymer, while mitigating the demands of environmental protection agencies.     

Biomass-based energy fuel through biochemical routes: A review

Energy demand is increasing continuously due to rapid growth in population and industrialization development. The development of energy sources is not keeping pace with spiraling consumption. Even developed countries are not able to compensate even after increasing the energy production multifold. The major energy demand is provided from the conventional energy sources such as coal, oil, natural gas, etc. Two major problems, which every country is facing with these conventional fuels, are depletion of fossil fuels and deterioration of environment.The present review article aims to highlight various biochemical processes for conversion of biomass into biological hydrogen gas and ethanol. The present discussion focuses on hydrogen production through various routes viz. fermentative, photosynthesis and biological water gas shift reaction. In addition, emphasis has been laid on ethanol as biomass-based energy fuel. The discussion has been focused on the technology for ethanol production from various biomass sources such as molasses, lignocellulosic feedstock and starch. Various biochemical processes and their major steps involved during the ethanol production from biomass have been discussed in detail.