Search Results (13)

Refining light and heavy oils in different proportions seems attractive, especially in cases of geopolitical, economic, environmental, and logistical constraints. The economical attractiveness could be undermined in cases where incompatibility occurs. The current study explores a highly complex refinery performance during processing a blend consisting of 17 crude oils of which one was extra light, five were light, nine were medium, and two were heavy. A n-heptane dilution test, using centrifugation, was employed to assess the colloidal stability of crude oils. In addition, a previously established correlation to relate crude oil vacuum residue fraction Conradson carbon content to asphaltene peptizability Sa according to ASTM D 7157 was also availed for the purpose of evaluating colloidal stability. It was found that the crude desalter amperage increases with the ${\displaystyle \frac{SBN}{IBN}}$ ratio and Sa reduction, reaching its maximum allowable value of 180 A at the ${\displaystyle \frac{SBN}{IBN}}$ ratio of 1.35, and Sa of 0.64. The ${\displaystyle \frac{SBN}{IBN}}$ ratio was found more reliable in predicting oil compatibility than the other ${\displaystyle \frac{SBN}{{IN}_{max}}}$ ratio used to assess colloidal stability in various research. Along with the increase in crude desalter amperage, fouling of the heat exchangers of a crude oil distillation plant was also recorded. An intercriteria analysis of process data together with crude composition data, and compatibility indices revealed that the amperage enhancement is statistically meaningfully related to an increase in the heaviest crude oil content in the process blend and the compatibility indices ${\displaystyle \frac{SBN}{IBN}}$ ratio and Sa, while the fouling was related only to the content of one of the light crude oils in the processed blend. Full article

The sol-gel process was used to create titanium dioxide (TiO₂) nanoparticles, a nanocrystalline semiconductor. How several synthesis factors, such as titanium precursor concentration, annealing temperature, and peptization temperature, affected the structural and morphological properties of TiO₂ nanoparticles were thoroughly explored. X-ray diffraction (XRD), infrared spectroscopy (IR), scanning electron microscopy (SEM), measurements of the specific surface area and pore size using the BET method, and UV-visible diffuse reflectance spectroscopy were all used in this investigation. The specific surface area determined by BET analysis decreased with increasing calcination temperature. The XRD analysis showed that a composite sample consisting mainly of anatase with minor brookite phases was obtained when the titanium precursor concentration ranged between 0.2 and 0.4 M, whereas a concentration of 0.5 M resulted in the formation of pure anatase. The photocatalytic activity of the synthesized TiO₂ powders under different operational parameters was evaluated for the common commercial textile dye, i.e., methylene blue (MB). It was experimented that the model pollutant decoloration follows the Langmuir–Hinshelwood (L-H) model. In view of this detailed research work, it was observed that the TiO₂ produced with a titanium precursor concentration of 0.3 M, a pH value of 5 during the peptization step, and an annealing temperature of 600 °C were found to be the best conditions for this catalytic degradation process. When used in conjunction with a TiO₂ concentration of 0.04 g/L and a reactor suspension pH value of 6.0, the TiO₂ catalyst produced a stunning 98% degradation of methylene blue under these circumstances. Full article

The environmental impact of industrial technologies and related remediation methods are major research trend lines. Unfortunately, in the development of materials for wastewater treatment or air purification, hazardous reactants are often employed, reducing the overall beneficial contribution of such technology on the environment. We here synthesize stable titanium dioxide (TiO₂) sols using a green route, with titanium tetraisopropoxide (TTIP) as precursor, water as solvent and acetic acid acting as catalyst, chelating agent and peptizing agent. The sol was deposited on glass by dip-coating and then analyzed using XRD, SEM and spectrophotometry. Wastewater purification ability was evaluated in the photocatalytic degradation of two organic dyes (Rhodamine B and Methylene Blue). Results on RhB showed > 85% degradation in 6 h maintained along a series of 7 tests, confirming good efficiency and reusability, and 100% in 3 h on MB; efficiency mostly depended on calcination temperature and layer thickness. High photodegradation efficiency was found in nonannealed samples, suggesting TiO₂ nanoparticles crystallization during sol–gel production. Yet, such samples showed a gradual decrease in photoactivity in repeated tests, probably due to a partial release of TiO₂ particles in solution, while on calcined samples a good adhesion was obtained, leading to a more durable photoactive layer. Full article

The study of the interactions between nanoparticles (NPs) and proteins has had a pivotal role in facilitating the understanding of biological effects and safe application of NPs after exposure to the physiological environment. Herein, for the first time, the interaction between L-methionine capped silver nanoparticles (AgMet), and bovine serum albumin (BSA) is investigated in order to predict the fate of AgMet after its contact with the most abundant blood transport protein. The detailed insights into the mechanism of interaction were achieved using different physicochemical techniques. The UV/Vis, TEM, and DLS were used for the characterization of the newly formed “entity”, while the kinetic and thermodynamic parameters were utilized to describe the adsorption process. Additionally, the fluorescence quenching and synchronous fluorescence studies enabled the prediction of the binding affinity and gave us insight into the influence of the adsorption on the conformation state of the BSA. According to the best of our knowledge, for the first time, we show that BSA can be used as an external stabilizer agent which is able to induce the peptization of previously agglomerated AgMet. We believe that the obtained results could contribute to further improvement of AgNPs’ performances as well as to the understanding of their in vivo behavior, which could contribute to their potential use in preclinical research studies. Full article

Compared to traditional membrane materials, alumina membranes are particularly beneficial for industrial wastewater treatment. However, the development of mesoporous α-alumina membranes for ultrafiltration applications is still a challenge due to uncontrolled pore size. In this study, we optimized the sol-gel method for the fabrication of a high-performance mesoporous α-alumina membrane. The peptization conditions (pH and peptization time) and phase transformation of boehmite were investigated to achieve better properties of the α-alumina membrane. The surface properties of the membrane were observed to be improved by reducing the system pH to 3.5 and increasing the peptization time to 24 h. The effect of sintering temperature on the phase transformation behavior, microstructures and performance of the membranes was also elucidated. An α-alumina ultrafiltration membrane with an average thickness of 2 μm was obtained after sintering at 1100 °C. The molecular weight cut-off of the α-alumina membrane, as obtained by the filtration of aqueous PEG solution, was approximately 163 kDa (12.5 nm). This is the smallest pore size ever reported for pure α-alumina membranes. Full article

The formation of sustainable concrete is directly relaed to the intensity of the processes occurring at the interface of phases. The study of the surface properties of CNPLUS carbon nanotubes in solutions of various plasticizers was carried out by measuring and calculating adsorption. The applicability of the adsorption value is for forecasting both the efficiency of dispersion and aggregative and sedimentative stability of the obtained dispersion systems. It was stated that two-dimensional pressure arising at the interface of adsorption layers in the dispersive medium with the surfactant Tensafor 2553.2 J/m² is sufficient to overcome adhesive strength on a small area of the localized contact of carbon nanoparticles CNPLUS, which explains the peptization and stabilization of the particles’ surface. It was established that full stabilization of nanoparticles in the aqueous dispersive medium could be ensured only by means of soap-like surfactants, with the compound potassium naphthalene sulfonate (Tensafor). It ensures formation of the micelle-like structure in coagulation layers that forms a structural and mechanical barrier with the external hydrophilic surface. This leads to the increase in the ultimate tensile strength of the concrete grout specimens by 38%. Full article

This work reviews an eco-friendly process for producing TiO₂ via colloidal aqueous sol–gel synthesis, resulting in crystalline materials without a calcination step. Three types of colloidal aqueous TiO₂ are reviewed: the as-synthesized type obtained directly after synthesis, without any specific treatment; the calcined, obtained after a subsequent calcination step; and the hydrothermal, obtained after a specific autoclave treatment. This eco-friendly process is based on the hydrolysis of a Ti precursor in excess of water, followed by the peptization of the precipitated TiO₂. Compared to classical TiO₂ synthesis, this method results in crystalline TiO₂ nanoparticles without any thermal treatment and uses only small amounts of organic chemicals. Depending on the synthesis parameters, the three crystalline phases of TiO₂ (anatase, brookite, and rutile) can be obtained. The morphology of the nanoparticles can also be tailored by the synthesis parameters. The most important parameter is the peptizing agent. Indeed, depending on its acidic or basic character and also on its amount, it can modulate the crystallinity and morphology of TiO₂. Colloidal aqueous TiO₂ photocatalysts are mainly being used in various photocatalytic reactions for organic pollutant degradation. The as-synthesized materials seem to have equivalent photocatalytic efficiency to the photocatalysts post-treated with thermal treatments and the commercial Evonik Aeroxide P25, which is produced by a high-temperature process. Indeed, as-prepared, the TiO₂ photocatalysts present a high specific surface area and crystalline phases. Emerging applications are also referenced, such as elaborating catalysts for fuel cells, nanocomposite drug delivery systems, or the inkjet printing of microstructures. Only a few works have explored these new properties, giving a lot of potential avenues for studying this eco-friendly TiO₂ synthesis method for innovative implementations. Full article

TiO₂ prepared by a green aqueous sol–gel peptization process is co-doped with nitrogen and zirconium to improve and extend its photoactivity to the visible region. Two nitrogen precursors are used: urea and triethylamine; zirconium (IV) tert-butoxide is added as a source of zirconia. The N/Ti molar ratio is fixed regardless of the chosen nitrogen precursor while the quantity of zirconia is set to 0.7, 1.4, 2, or 2.8 mol%. The performance and physico-chemical properties of these materials are compared with the commercial Evonik P25 photocatalyst. For all doped and co-doped samples, TiO₂ nanoparticles of 4 to 8 nm of size are formed of anatase-brookite phases, with a specific surface area between 125 and 280 m² g⁻¹ vs. 50 m² g⁻¹ for the commercial P25 photocatalyst. X-ray photoelectron (XPS) measurements show that nitrogen is incorporated into the TiO₂ materials through Ti-O-N bonds allowing light absorption in the visible region. The XPS spectra of the Zr-(co)doped powders show the presence of TiO₂-ZrO₂ mixed oxide materials. Under visible light, the best co-doped sample gives a degradation of p-nitrophenol (PNP) equal to 70% instead of 25% with pure TiO₂ and 10% with P25 under the same conditions. Similarly, the photocatalytic activity improved under UV/visible reaching 95% with the best sample compared to 50% with pure TiO₂. This study suggests that N/Zr co-doped TiO₂ nanoparticles can be produced in a safe and energy-efficient way while being markedly more active than state-of-the-art photocatalytic materials under visible light. Full article

The precursor for a lithium-ion sieve is prepared using an inorganic precipitation-peptization method with titanium sulfate as the titanium source and lithium acetate as the lithium source. The effects of Ni²⁺ (Nickel ions) doping on the stability of the sol, crystal morphology and interplanar spacing of Li₂TiO₃ are investigated. The results indicate that, after Ni²⁺ doping with varying fractions, the stability of the precursor sol first increases then decreases, and the maximum stabilization time of the precursor sol doped with 1% Ni²⁺ is 87 h. When doped with 1% Ni²⁺, the sol performance is most stable, the porous Li₂TiO₃ is obtained, and the specific surface area of Li₂TiO₃ increases by up to 1.349 m²/g from 0.911 m²/g. Accompanying the increase in calcination temperature, the inhibition of Ni²⁺ doping on the growth and crystallization of grains decreases. When the temperature is lower than 750 °C, Ni atoms replace the Ti atoms that are substituted for Li atoms in the original pure Li layer, forming lattice defects, resulting in the disappearance of (002) and (−131) diffraction peaks for Li₂TiO₃, the reduced ordering of crystal structure, a decrease in the interplanar spacing of the (002) plane, lattice expansion and an increase in the particle size to 100–200 nm. When the temperature exceeds 750 °C, with the increase of calcination temperature, the influence of Ni doping on the growth and crystallinity of grains decreases, and the (002) crystal surface starts to grow again. Full article

Laponite XLS™, which is a synthetic clay of nanometric dimensions containing a peptizing agent, has been associated with silanized hydroxypropylmethylcellulose (Si-HPMC) to form, after crosslinking, a novel composite hydrogel. Different protocols of sample preparation were used, leading to different morphologies. A key result was that the storage modulus of Si-HPMC/XLS composite hydrogel could be increased ten times when compared to that of pure Si-HPMC hydrogel using 2 wt % of Laponite. The viscoelastic properties of the composite formulations indicated that chemical and physical network structures co-existed in the Si-HPMC/XLS composite hydrogel. Images that were obtained from confocal laser scanning microscopy using labelled Laponite XLS in the composite hydrogels show two co-continuous areas: red light area and dark area. The tracking of fluorescent microspheres motions in the composite formulations revealed that the red-light area was a dense structure, whereas the dark area was rather loose without aggregated Laponite. This novel special double-network structure facilitates the composite hydrogel to be an adapted biomaterial for specific tissue engineering. Unfortunately, cytotoxicity’s assays suggested that XLS Laponites are cytotoxic at low concentration. This study validates that the hybrid interpenetrated network IPN hydrogel has a high modulus that has adapted for tissue engineering, but the cell’s internalization of Laponites has to be controlled. Full article

In this paper, TiO₂ prepared with an aqueous sol-gel synthesis by peptization process is doped with nitrogen precursor to extend its activity towards the visible region. Three N-precursors are used: urea, ethylenediamine and triethylamine. Different molar N/Ti ratios are tested and the synthesis is adapted for each dopant. For urea- and trimethylamine-doped samples, anatase-brookite TiO₂ nanoparticles of 6–8 nm are formed, with a specific surface area between 200 and 275 m²·g⁻¹. In ethylenediamine-doped samples, the formation of rutile phase is observed, and TiO₂ nanoparticles of 6–8 nm with a specific surface area between 185 and 240 m²·g⁻¹ are obtained. X-ray photoelectron spectroscopy (XPS) and diffuse reflectance measurements show the incorporation of nitrogen in TiO₂ materials through Ti–O–N bonds allowing light absorption in the visible region. Photocatalytic tests on the remediation of water polluted with p-nitrophenol show a marked improvement for all doped catalysts under visible light. The optimum doping, taking into account cost, activity and ease of synthesis, is up-scaled to a volume of 5 L and compared to commercial Degussa P25 material. This up-scaled sample shows similar properties compared to the lab-scale sample, i.e., a photoactivity 4 times higher than commercial P25. Full article

Recyclable aggregates of mesoporous titania with different anatase–rutile ratios have been prepared by thermal treatments of either amorphous or peptized precursors. These last two have been obtained by hydrolysis of either Ti(OC₂H₅)₄ or of Ti(OC₂H₅)₄ in mixture with 5 mol % Zr(OC₃H₇)₄ at room temperature in the presence of NH₄OH as a catalyzing agent. The anatase–rutile ratio, the recyclable aggregates of the nano-sized particles, the mesoporosity, the surface area and the crystallinity of the resulting crystallized products of titania can be controlled by the synthesis parameters including: concentration of ammonia catalyst, stirring time and concentration of the peptizing HNO₃, drying method of peptized precursors, calcination temperature, and finally the ramp rate up to the titania crystallization temperature. A broad range of synthesis parameters control the crystal sizes of titania particles produced. This allows catalyst preparation with very different crystal size, surface area, anatase to rutile crystal ratio and various mesoporous structures. Drying by lyophilization of precursors reduce the aggregation of the primary particles giving micro-/macroporous structures. Full article

A sulfur transfer agent in catalysts can effectively reduce the emission of SO₂ with minimum adverse effects on the catalytic cracking ability of the primary catalyst. In this paper, the composition and performance of sulfur transfer agents with different oxidative active components (such as Cu, Fe, Ni, Co, Ba, Zn and Cr) were prepared by acid peptization technique and characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and N₂ adsorption-desorption technique. The relationship between the composition and performance of the new sulfur transfer agents was investigated and the regeneration and recycling of the agents were performed. The results indicates that copper is a very good desulfurization active component. Moreover, the presence of CO has no significant effect on the absorption ability of SO₂ by the sulfur transfer agent. Full article