Effect of particle size on the rheology of Athabasca clay suspensions

The success of the separation process conventionally used in Alberta for oil sands extraction is highly influenced by the rheology of the oil sands slurry. In the gravity separation vessel, high slurry viscosities can hinder the rise of aerated bitumen and reduce the efficiency of the recovery process. In this study, the effect of particle size on the viscosity of oil sands slurries is investigated. Solids from mature fine tails (MFT) obtained from tailings pond were fractionated into three fractions of different particle size distributions and their rheological properties were studied. The solids in each fraction were characterized by XRD analysis which showed the presence of different types of clays in each fraction. For the rheological measurements, dispersions of the three fractions were prepared in the supernatant water decanted from centrifuged MFT to maintain the solution chemistry of the solids. Suspensions of each fraction showed a non‐Newtonian shear thinning behaviour as well as yield stress that is characteristic of structure formation within the suspensions. For all solids fractions, increasing solids concentration led to higher viscosities and higher yield stress values. Viscoelastic properties of the suspensions showed stronger solid‐like behaviour at higher particle concentrations. Among the three fractions numbered from 1 to 3, solids in fraction 3 were coated with organic matters, exhibiting the highest suspension viscosities. Also for fraction 3, higher gelling potency was observed at much lower weight fractions of solids as compared to the other fractions.     

The effect of NaCl and HPAM solution concentration on HPAM gel structure degradation by ultrasonic waves

The present study evaluated the impact of ultrasonic waves on the degradation of partially hydrolyzed polyacrylamide (HPAM) gel structures, focusing on the effects of sonication time, NaCl concentration, and HPAM solution concentration. Results showed that both sonication time and salinity levels play a crucial role in the degradation of HPAM gel, with an increase in sonication time leading to a decrease in the remaining gel and the presence of NaCl in the solution decreasing the residual time required for degradation. The results also revealed that higher levels of salinity expedite the degradation of the gel. In addition, the study discovered that a rise in polymer solution concentration usually results in a reduction in gel degradation. The research suggests there might be an ideal combination of polymer solution and NaCl concentration for achieving the greatest decrease in the degradation rate. For 2-min sonication, as the salinity of the HPAM solution, with a concentration of up to 5000 ppm, increases, the accumulated energy remains relatively constant. However, when the polymer solution concentration is increased, the accumulated energy becomes more sensitive to changes in salinity. The results of this study provide valuable insight into the interplay between polymer solution concentration, salt concentration, and the energy required for gel degradation, which can be applied in various fields including the oil and gas industry, petroleum processing, and environmental remediation.     

Determination of Pb2+ ions by a modified carbon paste electrode based on multi-walled carbon nanotubes (MWCNTs) and nanosilica

A novel carbon paste ion selective electrode for determination of trace amount of lead was prepared. Multi-walled carbon nanotubes (MWCNTs) and nanosilica were used for improvement of a lead carbon paste sensor response. MWCNTs have a good conductivity which helps the transduction of the signal in carbon paste electrode. The electrode composition of 20 wt% paraffin oil, 57% graphite powder, 15% ionophore (thiram), 5% MWCNTs, and 3% nanosilica showed the stable potential response to Pb²⁺ ions with the Nernstian slope of 29.8 (±0.2) mV decade^?1 over a wide linear concentration range of 10^?7–10^?2 mol L^?1. The electrode has fast response time, and long term stability (more than 2 months). The proposed electrode was used to determine the concentration of lead ions in waste water and black tea samples.     

Study on the efficiency of ethylene scavengers on the maintenance of postharvest quality of tomato fruit

The objectives of this study were to achieve the best level of each ethylene scavenger and evaluate the effect of selected levels of treatments on some quality traits of tomato during storage. Tomato fruits were subjected to four levels of treatments: palladium-promoted nano zeolite, KMnO₄-promoted nano zeolite, 1-MCP, CaCl₂, salicylic acid (SA) and UV-C. The sampling was done at 0, 7th, 14th, 21st, 28th and 35th days of cold storage. The results showed that palladium-promoted nano zeolite 5%, KMnO₄-promoted nano zeolite 20%, 1-MCP 30 ppm, CaCl₂ 2%, SA 1% and UV-C 15 min levels had the most ethylene scavenging function. Effectiveness of the treatments in ethylene scavenging was in the order: palladium?>?KMnO₄?>?1-MCP?>?SA?=?CaCl₂?>?UV-C. The palladium-promoted nano zeolite 5% had more positive effects on phenol content, polygalacturonase activity, lycopene content, fruit firmness and weight loss, and UV-C 15 min had effect on decay severity as compared to the other treatments. Overall, palladium-promoted nano zeolite 5% could be considered not only as favorable tool in tomato shelf life extension but also in preservation of quality characteristics of tomato fruits during storage. Moreover, the UV-C 15 min treatment could be an effective method for reducing decay severity and maintaining postharvest quality of tomato fruits.     

Synthesis and characterization of novel optically active and flame‐retardant heterocyclic polyimides

Tetrachlorophthalic anhydride (1) was reacted with L ‐leucine (2) in toluene solution at refluxing temperature in the presence of triethylamine and the resulting imide‐acid (4) was obtained in quantitative yield. The compound (4) was converted to the N‐(tetrachlorophthaloyl)‐L ‐leucine acid chloride (5) by reaction with thionyl chloride. The reaction of this acid chloride (5) with isoeugenol (6) was carried out in chloroform and novel optically active isoeugenol ester derivative (7) as a chiral monomer was obtained in high yield. The compound (7) was characterized by ¹H‐NMR, IR, Mass and elemental analysis, and then was used for the preparation of model compound (10) and polymerization reactions. 4‐Phenyl‐1,2,4‐triazoline‐3,5‐dione, PhTD (8) was allowed to react with compound (7). The reaction is very fast, and gives only one diastereomer of (10) via Diels–Alder and ene pathways in excellent yield. The polymerization reactions of novel monomer (7) with bistriazolinediones [bis‐(p‐3,5‐dioxo‐1,2,4‐triazolin‐4‐ylphenyl)methane (11) and 1,6‐bis‐(3,5‐dioxo‐1,2,4‐triazolin‐4‐yl)hexane] (12) were carried out in N,N‐dimethylacetamide (DMAc) at room temperature. The reactions are exothermic, fast, and give novel optically active polymers (13) and (14) via repetitive Diels–Alder‐ene polyaddition reactions. The resulting polymers are optically active, thermally stable, and flame resistant. All of the above compounds were fully characterized by IR, ¹H‐NMR, elemental analysis, and specific rotation. Some structural characterization and physical properties of these novel heterocyclic polyimides are reported. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 76: 240–248, 2000     

Simulation of Marangoni convection effects on the hydrodynamics of liquid–liquid extraction drops

Concentration induced Marangoni convection (MC) effect has many applications in the chemical engineering processes. In this study, the MC effects have been investigated in the toluene/acetone/water (T/A/W) liquid–liquid extraction system, focusing on the mass transfer and hydrodynamics. For the first time, the VOF-CSS model has been used, and the mass transfer equation has been coupled with the hydrodynamic equations of the VOF model, using the surface tension force model of the CSS. A single mass transfer equation has been solved for the two phases, modifying the unsteady, convective, and diffusive terms based on the equilibrium distribution coefficient. The MC effect has been implemented in the CSS surface tension model with a concentration-dependent surface tension coefficient. Simulations have been carried out in 1, 1.5, and 2?mm drops in the wide range of concentration (0.9–30?g/L). Good agreements have been achieved for the concentration and reduced velocity values compared with the existing experimental data. Simulation results showed that the reduced velocity values remain almost constant for every drop diameter, in the initial concentration range from 3.7 to 30?g/L. The reacceleration time for the three drop sizes with the different initial concentrations has been obtained from the simulation results and compared. The MC effects on the axial velocity profiles and drag coefficients were also reported providing comprehensive information about the MC effects on the hydrodynamics.     

Magnetic doping effects on the superconductivity of Y1-xMxBa2Cu3O7-δ (M = Fe,Co, Ni)

The discovery of superconductivity in copper oxide compounds has attracted considerable attention over the past three decades. The high transition temperature (T_c) in these compounds, exhibiting proximity to an antiferromagnetic order in their phase diagrams, remains one of the main areas of research. It is believed that magnetic fluctuations provide substance for the exotic superconductivity observed in these compounds. The present study attempts to introduce Fe, Co and Ni magnetic impurities into the superconducting cuprate YBa₂Cu₃O_7-δ with the aim of exploring the T_c behavior. The solid-state synthesis method is exploited to prepare fully oxygenated Y_1-xM_xBa₂Cu₃O_7-δ (Y_1-xM_x-123) (M = Co, Fe, Ni) samples with low levels of doping (0.00000 ≤ x ≤ 0.03000). Systematic measurements are then employed to assess the synthesized samples using AC magnetic susceptibility, electrical resistivity and X-ray diffraction (XRD). The measurements revealed an increase in T_c as a result of magnetic substitution for Y. However, the study of non-magnetic dopings on the fully oxygenated Y_1-xM'_xBa₂Cu₃O_7-δ (Y_1-xM'_x-123) (M' = Ca, Sr) samples showed a decrease in T_c. Quantitative XRD analysis further suggested that the internal pressure could have minor effects on the increase in T_c. The normal state resistivity vs temperature showed a linear profile, confirming that the samples are at an optimal doping of the carrier concentration.     

A Simple Investigation of the Thermal Effusivity of Silver Nanofluid Using Photopyroelectric Technique

We investigated the thermal effusivity of silver nanofluids using a microwave technique. During microwave irradiation, silver nanoparticles with a narrow particle size distribution were formed in water and in ethylene glycol, with a polyvinylpyrrolidone stabilizer. We designed and used a front-photopyroelectric technique that employed a metalized polyvinylidene difluoride (PVDF) pyroelectric sensor, with a thermally thick sensor and sample. Using this technique, we calculated the thermal effusivity of the silver nanofluids at a given frequency using the combination of the signal’s normalized amplitude–phase. The thermal effusivity of the nanofluids increased with the number of microwave irradiation cycles, which increased the nanoparticle concentration in the base fluids. A comparison with reported values illustrates the high accuracy obtained from the results of thermal diffusivity, the thermal effusivity of the PVDF sensor, and the thermal effusivity of ethylene glycol as a base fluid (differing by only 1.7 %, 0.5 %, and 2.3 %, respectively). Our method can therefore be used to study nanofluids with varying nanoparticle properties, such as concentration, size, and shape.