Structural and magnetic properties of Li2O–Fe2O3 ceramic nanostructures

xLi₂O–(1−x)α-Fe₂O₃ (x=0.1, 0.3, 0.5, and 0.7) nanoparticle systems were successfully synthesized by mechanochemical activation of Li₂O and α-Fe₂O₃ mixtures for 0–12 h of ball milling time. The study aims at exploring the formation of magnetic oxide semiconductors at the nanoscale, which is of crucial importance for catalysis, sensing and electrochemical applications. X-ray powder diffraction (XRD), Mössbauer spectroscopy and magnetic measurements were used to study the phase evolution of xLi₂O–(1−x)α-Fe₂O₃ nanoparticle systems under the mechanochemical activation process. Rietveld refinement of the XRD patterns yielded the values of the particle size as function of composition and milling times and indicated the presence of Li-substituted hematite and tetra lithium iron oxide LiFeO₂, along with the formation of multiple phases for large x values and long milling times. The Mössbauer studies showed that the spectrum of the mechanochemically activated composites evolved from a sextet for hematite to sextets and a doublet upon duration of the milling process with lithium oxide. Magnetic measurements recorded at 5 K to room temperature (RT) in an applied magnetic field of 50,000 Oe showed that the magnetization of the milled samples is larger at low temperatures than at RT and increases with decreasing particle size. Zero field cooling measurements made possible the determination of the blocking temperatures of the specimens as function of ball milling time and evidenced the occurrence of superparamagnetism in the studied samples. This result correlates well with the observed presence of a quadrupole-split doublet in the Mössbauer spectra.     

Evaluation of Low‐Cost Separators for Increased Power Generation in Single Chamber Microbial Fuel Cells with Membrane Electrode Assembly

We compared novel size‐selective separators, namely the textile fabrics of polyphenylene sulfide (PPS) and sulfonated polyphenylene sulfide (S‐PPS), and the nonwoven fabrics of polypropylene80 (PP 80) and PP 100, with commonly used ion exchange separators (Nafion 117 and cation exchange membane‐7000; CMI‐7000) in terms of power generation, oxygen diffusion, and biofilm formation in a single chamber microbial fuel cell. Size‐selective separators exhibited more power generation than ion selective separators. MFC operation with size‐selective separators generated power output ranging 0.407 to 0.591 V (1000 Ω), whereas with Nafion it was 0.272 V. In polarization analysis, S‐PPS resulted in the highest power density of 190 mW/m², whereas it was 24 mW/m² with Nafion‐117. Size selective separators showed similar or higher proton conductivity than Nafion 117. Oxygen mass transfer coefficients of size‐selective separators (K_O = 3.7 ∼ 7.5 × 10⁻⁵) were lower or similar to Nafion (K_O = 7.5 × 10⁻⁵). Fourier‐transform infrared spectroscopy and scanning electron microscopy analysis revealed that all separators (PP80, S‐PPS, and Nafion) contained proteins or carbon chain compounds after 300‐day operation, and however, Nafion 117 seems to be more susceptible to biofouling than the other separators.     

Incorporation of the transition metals (Cr and Fe) into β-SiAlON crystal structure

Outstanding properties for SiAlON ceramics can be obtained by tailoring the microstructure through α-SiAlON and β-SiAlON phase content as well as a type of secondary phases. It is so far well known that while some of the elements could be accommodated in α-SiAlON structure, β-SiAlON does not easily accommodate different elements in its structure. In this work, SiAlON ceramics were produced by using β-Si₃N₄ starting powder containing small amount of iron and chromium and the possible incorporation of iron and chromium into β-SiAlON structure was investigated by using analytical transmission electron microscopy (TEM) techniques. As a result of analytical TEM analysis, it is found that transition metals (Cr and Fe) can enter into the β-SiAlON crystal structure.     

Hydrothermal synthesis and tuning of size and morphology of α-Co(OH)2 and α-Co2(OH)3Cl nanostructures as precursors for nanosized Co3O4

This study aims to investigate the hydrothermally synthesized cobalt(II) hydroxide-based materials, which will be thermally converted to generate Co₃O₄ nanostructures; an important class of materials characterized by good electrochemical, catalytic and optical properties. First, cobalt(II) hydroxide nanostructures were prepared via hydrothermal hydrolysis of two different precursors (cobalt(II) chloride salt and dichlorobis(thiourea)cobalt(II) complex) exposure to an ammonia atmosphere, and then the obtained α-Co(OH)₂ and α-Co₂(OH)₃Cl nanostructures were calcined to produce Co₃O₄ nanostructures that were characterized by FT-IR, XRD, UV–vis DRS and SEM techniques. The effects of the nature of the precursor, its concentration, and of the temperature and reaction time on size and morphology of the product were also investigated.     

Determination of translucent content in mangosteen by means of near infrared transmittance

Translucent flesh disorder is undesirable in mangosteen meant for export. However, mangosteens are judged as translucent when the translucent flesh is visible on the pulp surface regardless of the quantity of the internal translucent flesh which may result in some mangosteen assessed as normal having the same amount of translucent flesh content as a mangosteen judged as translucent. The critical amount of translucent flesh to be visible on the pulp surface needs to be determined for assessment purposes. A non-destructive technique to measure the translucent content is a practical tool as the first step towards the establishment of the critical value.A non-destructive model was developed to estimate the translucent content in mangosteens using near infrared transmittance. The translucent area of the flesh section on the fruit surface was used to indicate the translucent content. The effects of the orientation of the fruit and also of the light source to the relative position of the detector as well as the effect of the measurement position of the fruit on the predictive performance were examined. The results showed that the best partial least squares model was achieved with spectra acquired from the fruit position which revealed the largest flesh segment (prediction correlation coefficient was 0.86 and root mean square error of prediction was 7.58%). The horizontal stem-calyx fruit axis and a 135° angle from the light source relative to the detector were the optimal fruit orientation and configuration for measurement.     

Improving the transfer of near infrared prediction models by orthogonal methods

Eight calibration transfer methods based on the removal of orthogonal signal were compared for the standardization of whole soybean protein and oil models. Dynamic orthogonal projection (DOP), transfer by orthogonal projection (TOP), error removal by orthogonal subtraction (EROS), orthogonal signal correction (OSC), and orthogonal projections to latent structures (O-PLS) as well as the modification and extension of some of these methods were compared in the transfer of models in intra and inter-brand situations using two Foss Infratecs and two Bruins OmegAnalyzerGs. For each brand, a master was designated and its models transferred onto the second unit of its network and the two units of the second brand. Calibration models were transferable from brand to brand with similar or better precision than when each instrument was calibrated on its own calibration set (for Infratec 1229, the relative predictive determinant (RPD) increased in intra and inter-brand calibration transfer situations from 10.42 to 11.45 and 10.57, with DOP and EROS respectively). Performance of each method was different across parameters, instruments, and validation sets. DOP modifications on the determination of the difference matrix showed promising results while TOP and EROS extensions to include variability specifically present in certain crop years did not bring any beneficial effects.     

Determination of Asphalt Cement Properties by Near Infrared Spectroscopy and Chemometrics

Abstract

In the present study, near infrared (NIR) spectroscopy and chemometrics techniques have been combined to predict some properties used to characterize and to classify asphalt cement grade. Principal Components Regression (PCR) and Partial Least Squares Regression (PLSR) were employed to develop linear models to predict penetration value, absolute viscosity at 60°C, kinematic viscosity at 135°C and flash point of asphalt cements. The good correlation between NIR pretreated spectra and the properties investigated, measured by values of correlation coefficients and root mean squared errors of both calibration and prediction are here discussed. It was concluded that the combination of both techniques can be used to predict properties of asphalt cement to be delivered after on-line blending of hard and soft binders stocked in refineries.     

Experimental and Molecular Dynamics Simulations of Tribochemical Reactions with ZDDP: Zinc Phosphate–Iron Oxide Reaction

Zinc phosphate glass is considered to be the main constituent of tribofilms generated under boundary lubrication with zinc dialkyldithiophosphate (ZDDP), a well-known antiwear additive. The reaction occurring during friction between zinc phosphate glasses and steel native iron oxide layer is investigated by both an experimental approach and by Molecular Dynamics simulations (MD). The importance of this “tribochemical” reaction in the general ZDDP antiwear process is discussed.     

Cathodic disbondment of epoxy coating with zinc aluminum polyphosphate as a modified zinc phosphate anticorrosion pigment

As an approach to improve the resistance of protective coatings to the disbondment, modification of the formulation through incorporation of zinc aluminum polyphosphate anticorrosion pigment representing third generation phosphates was examined in this paper. The data obtained from cathodic disbonding test, electrochemical impedance spectroscopy and pull-off indicated that introduction of zinc aluminum polyphosphate within epoxy coating could provide improved resistance to cathodic disbonding as well as superior adhesion strength. The superiority in the presence of the modified pigment was connected to deposition of a layer at the disbonding front and locally controlled pH as well. The precipitation restricting active zone available for electrochemical reaction was confirmed by SEM.     

Filtration effectiveness of HVAC systems at near‐roadway schools

Concern for the exposure of children attending schools located near busy roadways to toxic, traffic‐related air pollutants has raised questions regarding the environmental benefits of advanced heating, ventilation, and air‐conditioning (HVAC) filtration systems for near‐road pollution. Levels of black carbon and gaseous pollutants were measured at three indoor classroom sites and at seven outdoor monitoring sites at Las Vegas schools. Initial HVAC filtration systems effected a 31–66% reduction in black carbon particle concentrations inside three schools compared with ambient air concentrations. After improved filtration systems were installed, black carbon particle concentrations were reduced by 74–97% inside three classrooms relative to ambient air concentrations. Average black carbon particle concentrations inside the schools with improved filtration systems were lower than typical ambient Las Vegas concentrations by 49–96%. Gaseous pollutants were higher indoors than outdoors. The higher indoor concentrations most likely originated at least partially from indoor sources, which were not targeted as part of this intervention.