Preparation and Characterization of Date Palm Bio-Oil Modified Phenolic Foam.

In this work, the potential of biomass-derived date palm bio-oil as a partial substitute for phenol in the phenolic resin was evaluated. Date palm bio-oils derived from date palm were used for the partial substitution of phenol in the preparation of phenolic foam (PF) insulation materials. Date palm waste material was processed using pyrolysis at 525 °C to produce bio-oil rich in phenolic compounds. The bio-oil was used to partially replace phenol in the synthesis of phenolic resin, which was subsequently used to prepare foams. The resulting changes in the physical, mechanical, and thermal properties of the foams were studied. The substituted foams exhibited 93%, 181%, and 40% improvement in compressive strength with 10%, 15%, and 20% bio-oil substitution, respectively. Due to the incorporation of biomass waste material, the partial reduction in phenol uses, and the favorable properties, the date palm bio-oil substituted phenolic foams are considered more environmentally benign alternatives to traditional phenolic foams.

Clay-Alginate Beads Loaded with Ionic Liquids: Potential Adsorbents for the Efficient Extraction of Oil from Produced Water.

Produced water (PW) generated from the petroleum industry, during the extraction of oil and gas, has harmful impacts on human health and aquatic life, due to its complex nature. Therefore, it is necessary to treat it before discharging it into the environment in order to avoid serious environmental concerns. In this research, oil adsorption from PW was investigated using clay-alginate beads loaded with ionic liquids (ILs), as the adsorbent material. The effects of several process parameters, such as the initial concentration of oil, contact time, pH, and temperature on the removal efficiency of the beads, were analyzed and optimized. Different characterization methods, such as the Fourier transform infrared spectrophotometer (FTIR), scanning electron microscopy (SEM), energy dispersive X-ray (EDX), and thermal gravimetric analysis (TGA), were used to investigate the surface morphology, the chemical bond structure and functional group, and the thermal stability of the ILs-based beads. The results revealed that the clay-alginate-ILs beads indicated a removal efficiency of 71.8% at the optimum conditions (600 ppm initial oil concentration, 70 min contact time, 10 pH, and at room temperature) with an adsorption capacity of 431 mg/g. The FTIR analysis confirmed the successful chemical bond interaction of the oil with the beads. The SEM analysis verified that the beads have a porous and rough surface, which is appropriate for the adsorption of oil onto the bead's surface. The TGA analysis provides the thermal degradation profile for the clay-alginate-ILs. The beads used in the adsorption process were regenerated and used for up to four cycles.

Ionic Liquid Agar-Alginate Beads as a Sustainable Phenol Adsorbent.

Cleaning wastewater containing low concentrations of phenolic compounds is a challenging task. In this work, agar-alginate beads impregnated with trihexyltetradecylphosphonium bromide ([P66614][Br]) ionic liquid adsorbent were synthesized as a potential adsorbent for such applications. FTIR, TGA, SEM, EDX and PZC studies were performed to characterize and understand the physicochemical properties of the adsorbent. The Fourier transformation infrared spectroscopy (FTIR) study showed that [P66614][Br] ionic liquid was effectively incorporated into the agar-alginate structure. TGA and SEM confirmed comparative enhanced thermal stability and porous surface, respectively. Chemical reaction rate-altering parameters, i.e., pH, contact time, initial phenol concentration and temperature, are optimized at highest phenol removal. It was found that the maximum phenol adsorption capacity and highest removal efficiency by the adsorbent occurred at pH 2, initial phenol concentration of 150 mg/L, beads dosage of 6 mg/mL and contact time of 2 h with values of 16.28 mg/g and 65.12%, respectively. The pseudo-second order model fitted the adsorption kinetics well, and the Freundlich isotherm model gave the experimental data the best fit. Analysis of thermodynamic data demonstrated that the adsorption process is fundamentally exothermic in nature, and low temperature favors spontaneity of the chemical reaction. Regeneration studies indicated that the adsorbent can at least be used for four cycles in such applications without any considerable loss in adsorption efficiency.

Ionic liquids and deep eutectic solvents for the recovery of phenolic compounds: effect of ionic liquids structure and process parameters.

Water pollution is a severe and challenging issue threatening the sustainable development of human civilization. Besides other pollutants, waste fluid streams contain phenolic compounds. These have an adverse effect on the human health and marine ecosystem due to their toxic, mutagenic, and carcinogenic nature. Therefore, it is necessary to remove such phenolic pollutants from waste stream fluids prior to discharging to the environment. Different methods have been proposed to remove phenolic compounds from wastewater, including extraction using ionic liquids (ILs) and deep eutectic solvent (DES), a class of organic salts having melting point below 100 °C and tunable physicochemical properties. The purpose of this review is to present the progress in utilizing ILs and DES for phenolic compound extraction from waste fluid streams. The effects of IL structural characteristics, such as anion type, cation type, alkyl chain length, and functional groups will be discussed. In addition, the impact of key process parameters such as pH, phenol concentration, phase ratio, and temperature will be also described. More importantly, several ideas for addressing the limitations of the treatment process and improving its efficiency and industrial viability will be presented. These ideas may form the basis for future studies on developing more effective IL-based processes for treating wastewaters contaminated with phenolic pollutants, to address a growing worldwide environmental problem.

Fluorescent aminal linked porous organic polymer for reversible iodine capture and sensing.

A novel triazene-anthracene-based fluorescent aminal linked porous organic polymer (TALPOP) was prepared via metal free-Schiff base polycondensation reaction of 9,10-bis-(4,6-diamino-S-triazin-2-yl)anthracene and 2-furaldehyde. The polymer has exceptional chemical and thermal stabilities and exhibit good porosity with Brunauer-Emmett-Teller surface area of 401 m2g-1. The combination of such porosity along with the highly conjugated heteroatom-rich framework enabled the polymer to exhibit exceptional iodine vapor uptake of up to 314 wt % and reversible iodine adsorption in solution. Because of the inclusion of the anthracene moieties, the TALPOP exhibited excellent detection sensitivity towards iodine via florescence quenching with Ksv value of 2.9 × 103 L mol-1. The cost effective TALPOP along with its high uptake and sensing of iodine, make it an ideal material for environmental remediation.

Thermal Conductivities of Choline Chloride-Based Deep Eutectic Solvents and Their Mixtures with Water: Measurement and Estimation.

The thermal conductivities of selected deep eutectic solvents (DESs) were determined using the modified transient plane source (MTPS) method over the temperature range from 295 K to 363 K at atmospheric pressure. The results were found to range from 0.198 W·m-1·K-1 to 0.250 W·m-1·K-1. Various empirical and thermodynamic correlations present in literature, including the group contribution method and mixing correlations, were used to model the thermal conductivities of these DES at different temperatures. The predictions of these correlations were compared and consolidated with the reported experimental values. In addition, the thermal conductivities of DES mixtures with water over a wide range of compositions at 298 K and atmospheric pressure were measured. The standard uncertainty in thermal conductivity was estimated to be less than ± 0.001 W·m-1·K-1 and ± 0.05 K in temperature. The results indicated that DES have significant potential for use as heat transfer fluids.

Application of multiwalled carbon nanotubes and its magnetite derivative for emulsified oil removal from produced water.

Multiwalled carbon nanotubes and their magnetite derivatives were employed as adsorbents for emulsified oil removal from produced water. The experimental parameters for maximum emulsified oil removal efficiency and effective regeneration of these adsorbents were determined. The optimum parameters in terms of adsorbent dosage, contact time, salinity, pH and temperature were 3.0 g/L, 20.0 min, 0 ppm, 7.0 and 25°C for both adsorbents. Due to their low density, multiwalledcarbon nanotubes could not be successfully employed in packed bed columns. The magnetite derivative has a larger density and hence, for the removal of emulsified oil from produced water packed bed column studies were performed utilizing multiwalled carbon magnetite nanotubes. The packed bed column efficiency and behaviour were evaluated using Thomas, Clark, Yan et al. and Bohart and Adams models. The Yan model was found to best describe the column experimental data. The adsorbents were regenerated using n-hexane and reused several times for oil removal from produced water without any significant decrease in their initial adsorption capacities.

Assessment of using unleaded fuel in the harsh environment of the United Arab Emirates.

The service life of lubricating oil produced in the United Arab Emirates (UAE) was examined using a car fueled with leaded or unleaded gasoline of the same grade in harsh local conditions. In addition, the economic impact of using leaded vs. unleaded gasoline via the effects on the useful life of engine oil was investigated. Every 500 km that the car was operated, the physical properties of the oil were examined to determine the optimum oil life before replacement. It was found that relative to unleaded gasoline, leaded gasoline resulted in a faster deterioration of lube oil properties and a reduced useful life of the oil. Many of the effects of use on the physical properties of oil became apparent from the beginning of its service, especially when leaded gasoline was used. Our findings indicate that the recommended useful life of oil when using leaded gasoline is 2500 km. With unleaded gasoline, deterioration of the physical properties of the lubricating oil became a concern after 3000 km. Thus with unleaded gasoline, it is recommended to have an oil change every 3500 km. These findings indicate that the decision of the UAE government to stop using lead compound additives to improve the octane number of gasoline will not only protect the environment from the harmful effects of lead compounds, but will also extend the useful life of oil. This extension will reduce the amount of used oil that is disposed of by up to 4678 tons/year. This reduction in oil use translates to a cost savings of about 23.4 million UAE Dirhams (=$6.37 million US Dollars) per year.

Molecular modeling study of the aggregation behavior of nickel(II), cobalt(II), lead(II) and zinc(II) bis(2-ethylhexyl) phosphate complexes.

The physiochemical nature of the metal-extractant species in organic solvent has been a matter of debate over liquid-liquid extraction of transition metals by bis(2-ethylhexyl) phosphate. The aggregation behavior of nickel(II), cobalt(II), lead(II), and zinc(II) bis(2-ethylhexyl) phosphate have been investigated using molecular modeling. The recently confirmed "open" water channels rodlike reversed micelles which is in contact with the nonaqueous solvent rather than in an inner core (or "closed" water channel) of the nickel-extractant species by Ibrahim and Neuman appears to be a unique structure for such species. Lead-, cobalt- and zinc-extractant species behave in a different manner. The cobalt-extractant species form rodlike reversed micelles, but does not show the formation of any open water channel. The zinc- and lead-extractant species form ellipsoidal (or deformed spherical) reversed micelles with fewer water molecules located at the core of the micelles which is in accord with the conventional view of reversed micelles. The structural variations of the reversed micelles for the metal extracted species are in accord with the known extraction behavior of such metals when using HDEHP.

Nanostructure of open water-channel reversed micelles. I. 1H NMR spectroscopy and molecular modeling.

A recently proposed model for the rodlike reversed micelles of nickel(II) bis(2-ethylhexyl)phosphate is examined in greater detail using 1H NMR spectroscopy and molecular modeling. 1H NMR spectra show that the solubilized water molecules are situated in a different environment compared with the water molecules in classical (AOT) reversed micelles. Geometry optimization and molecular dynamics simulation clearly indicate that the water molecules are not located in the interior core of the reversed micelles, but instead the water molecules exist in compartments or channels in the surface of these rodlike reversed micelles, thereby confirming the open water-channel model of reversed micelles. Molecular modeling was also employed to examine the effects of surfactant molecular structure, cosurfactant, solvent aromaticity, and temperature on the nanostructure of the reversed micellar aggregates. It is significant that molecular modeling provides an interpretation of the nanostructure of reversed micellar aggregates that is consistent with a variety of known experimental observations reported in the liquid/liquid extraction literature. These findings show that the structure of reversed micelles is much richer at the nanoscale level than previously recognized.

New Approach to the Study of Particle-Surface Adhesion Using Atomic Force Microscopy.

The colloidal probe technique is commonly employed to determine the adhesion force between a particle and a solid surface. Characterization of the adhesion of a particle across a surface can be as important, if not more so, as the determination of an average value for the adhesion. Unfortunately, the measurement of the variation in adhesion can be difficult at best. A new approach for studying particle-surface adhesion based on the force-volume technique is presented. Upon combining the force-volume technique with a colloidal probe, not only is it possible to determine the average adhesion force, but an image of the spatial variation of the adhesion can also be obtained. This method is envisioned to have great potential for examining and analyzing the adhesion behavior in complex natural and technological systems. Copyright 2000 Academic Press.