Commercial bentonites as detoxifier of broiler feed contaminated with aflatoxin

Some bentonites have been probed to be efficient as sequestering agents for aflatoxins; they decreased the bioavailability of the toxin in the gastrointestinal tracts of birds when they are incorporated in the diets. The binding capacity of these adsorbents varied with the rheological source and even among batches of a given source. Three bentonites from different sources in Argentina, which have very different aflatoxins (AFs) adsorption capacity, were studied. The characterization comprises chemical analysis, scanning electron microscopy (SEM), X-ray power diffraction (XRD), Hg intrusion porosimetry, swelling capacity, etc. The main factors affecting the adsorption of AFs seem to be related to the isomorphic substitution of the montmorillonite and to electrostatic interactions generated by the surface charge of the samples. Neither the mean pore size nor the percentage of quartz has any effect upon the AFs adsorption.     

Identification of phases and precipitates by AFM in duplex stainless steel unions

ABSTRACT

Atomic Force Microscopy (AFM), a characterization technique that generates topographic images of surfaces at very high resolutions, works by recording the surface relief details of the material with a cantilever which moves over the sample, while a piezoelectric sensor monitors changes in height. This technique is useful for identifying phases, particles and precipitates on a nanoscale and is therefore proposed for identifying them in the fusion zone of welded components and for early identification of faults due to cracking. This is a technique that does not require conductive samples, or special metallographic preparation of specimens as is the case with electron microscopy. The material studied is a duplex 2205 stainless steel, welded by means of gas tungsten arc welding (GTAW). The welded material was subjected to stress tests. The test specimens were characterized using optical microscopy, scanning electron microscopy, atomic force microscopy and nanoindentation tests. The results focus on the identification of the specific magnetic, topographic and hardness characteristics of each of the phases, particles and areas present in the base metal, the fusion zone and the zone deformed by the fracture.     

Evaluation of susceptibility of hydrogen-induced cracking in micro-alloyed armour steel welds using a geometry-modified implant test

Susceptibility to hydrogen-induced cracking (HIC) was evaluated in steel welds for quenched and tempered armouring steel of 4.5 mm thickness. The welds were produced using the shielded metal arc welding process with low heat support and AWS E11018M 2.4 mm consumable. The susceptibility to HIC was evaluated by means of an implant test with modified geometry in welded joints with and without preheating being applied, using consumables in ideal stock conditions and exposed to the atmosphere. It was found that the consumable stock conditions were more relevant than preheating in regard to susceptibility to HIC.     

Effect of the Nucleophile’s Nature on Chloroacetanilide Herbicides Cleavage Reaction Mechanism. A DFT Study

In this study, the degradation mechanism of chloroacetanilide herbicides in the presence of four different nucleophiles, namely: Br⁻, I⁻, HS⁻, and S₂O₃⁻², was theoretically evaluated using the dispersion-corrected hybrid functional wB97XD and the DGDZVP as a basis set. The comparison of computed activation energies with experimental data shows an excellent correlation (R² = 0.98 for alachlor and 0.97 for propachlor). The results suggest that the best nucleophiles are those where a sulfur atom performs the nucleophilic attack, whereas the other species are less reactive. Furthermore, it was observed that the different R groups of chloroacetanilide herbicides have a negligible effect on the activation energy of the process. Further insights into the mechanism show that geometrical changes and electronic rearrangements contribute 60% and 40% of the activation energy, respectively. A deeper analysis of the reaction coordinate was conducted, employing the evolution chemical potential, hardness, and electrophilicity index, as well as the electronic flux. The charge analysis shows that the electron density of chlorine increases as the nucleophilic attack occurs. Finally, NBO analysis indicates that the nucleophilic substitution in chloroacetanilides is an asynchronous process with a late transition state for all models except for the case of the iodide attack, which occurs through an early transition state in the reaction.     

High accumulation of perfluorooctane sulfonate (PFOS) in marine tucuxi dolphins (Sotalia guianensis) from the Brazilian coast

Perfluorooctane sulfonate (PFOS) and other perfluoroalkyl compounds (PFCs) were measured in liver samples from 29 marine tucuxi dolphins from Rio de Janeiro state (RJ), Brazil. PFC measurement combined liquid chromatography and mass spectrometry, using a CapLC system connected to a Quadrupole-LIT mass spectrometer. PFOS was the only PFC detected and it was so in all samples. PFOS concentrations (ng x g(-1) dw) of dolphins (n=23) from the highly contaminated Guanabara Bay (in RJ) varied between 43 and 2431 as well as between 76 and 427 from areas of RJ other than the quoted bay (n=6). Concentrations of three fetuses and one neonate varied between 664 and 1590. Fetus/mother ratios were calculated in two situations (2.75 and 2.62). It seems that mother-to-calf transference plays important role for relationships between PFOS and age. When a one-year-old male calf presenting 2431 ng x g(-1) dw was excluded from the test, significant correlations were observed between PFOS concentrations and both age and total length. Despite the placental transference, PFOS concentrations were not significantly lower in females than in males. PFOS levels in marine tucuxi dolphins from Guanabara Bay are among the highest detected to date in cetaceans, and this may represent a threat to the small population concerned.     

Comparison of static and step-pulsed ultra-high pressure on the microbial stability of fresh cut pineapple

Fresh cut pineapple cubes inoculated with 10^4–5 CFU g⁻¹ Saccharomyces cerevisiae were packed in heat-sealed polyethylene pouches and subjected at ambient temperature to static and step-pulsed ultra-high pressure (UHP) treatments. Static treatments included 100 and 9000 s at 270 MPa and 9000 s at 340 MPa. Step-pulsed pressure treatments included 100, 300 and 600 s at 0–270 MPa using 0·5-s and 10-s pulses. Inoculated treated and untreated samples were held at 4°C for 60 days. Bacteria and yeast counts were determined using plate count agar and yeast extract peptone dextrose agar, respectively. Static treatment at 270 and 340 MPa for 9000 s resulted in <240 CFU g⁻¹ yeast and bacteria counts for up to 60 days. Step-pulsed pressure treatments for 100 s at 0–270 MPa using 0·5-s (200 pulses) and 10-s pulses (10 pulses) were more effective than a 100-s static 270-MPa treatment. Step-pulsed pressure treatments (300 and 600 s) using 0·5-s pulses (600 and 1200 pulses) and 10-s pulses (30 and 60 pulses) were as effective as 9000-s static pressure treatments at 270 and 340 MPa. This storage study confirmed the superiority of step-pulsed over static pressure treatments. © 1998 SCI.     

ELECTROPHORETIC MOBILITY AND STABILIZATION OF ASPHALTENES IN LOW CONDUCTIVITY MEDIA

ABSTRACT

The electrophoretic mobilities of asphaltenes in n-heptane and ethanol were determined. The asphaltenes studied show a positive charge in both solvents. However, the magnitude of the charge is considerably lower in n-heptane than in ethanol. It is concluded that although the electrostatic forces are presented in both solvents, the van der Waals’ atractive forces are the main responsable for the flocculation of asphaltene particles. The addition of a well known asphaltene stabilizer, dodecyl benzene sulphonic acid (DBSA), decreases the electrophoretic mobility of asphaltene particles in ethanol until a constant positive value is reached. This means that the neutralization of the positive charges of the asphaltene particles is not complete, probably due to the limited adsorption of the DBSA on asphaltene surface and also, to the presence of charges inside the asphaltene particles that are not accessible to the DBSA.     

Collection zone kinetic model for industrial flotation columns

The collection zone recovery of a flotation column was modeled using a rectangular distribution function for the kinetic rate constant and a tank in series model with different vessel sizes for the residence time distribution. It was demonstrated that an analytical expression can be obtained and that data from large industrial columns fits well, keeping the parsimony principle by using a simple and practical solution. An example for the estimation of the maximum kinetic rate constant, useful for scale-up purposes, is shown using data from industrial flotation columns.