Break oily water emulsion during petroleum enhancing production processes using green approach for the synthesis of SnCuO@FeO nanocomposite from microorganisms.

The aim of this work was to synthesize a green nanoparticle SnCuO@FeO nanocomposite core-shell to break oily water emulsions during petroleum-enhancing production processes as an alternative to chemical and physical processes. In this study, eight bacterial isolates (MHB1-MHB8) have been isolated from tree leaves, giant reeds, and soil samples. The investigation involved testing bacterial isolates for their ability to make FeO nanoparticles and choosing the best producers. The selected isolate (MHB5) was identified by amplification and sequencing of the 16S rRNA gene as Bacillus paramycoides strain OQ878685. MHB5 produced the FeO nanoparticles with the smallest particle size (78.7 nm) using DLS. XRD, FTIR, and TEM were used to characterize the biosynthesized nanoparticles. The jar experiment used SnCuO@FeO with different ratios of Sn to CuO (1:1, 2:1, and 3:1) to study the effect of oil concentration, retention time, and temperature. The most effective performance was observed with a 1:1 ratio of Sn to CuO, achieving an 85% separation efficiency at a concentration of 5 mg/L, for a duration of 5 min, and at a temperature of 373 K. Analysis using kinetic models indicates that the adsorption process can be accurately described by both the pseudo-first-order and pseudo-second-order models. This suggests that the adsorption mechanism likely involves a combination of film diffusion and intraparticle diffusion. Regarding the adsorption isotherm, the Langmuir model provides a strong fit for the data, while the D-R model indicates that physical interactions primarily govern the adsorption mechanism. Thermodynamic analysis reveals a ∆H value of 18.62 kJ/mol, indicating an exothermic adsorption process. This suggests that the adsorption is a favorable process, as energy is released during the process. Finally, the synthesized green SnCuO@FeO nanocomposite has potential for use in advanced applications in the oil and gas industry to help the industry meet regulatory compliance, lower operation costs, reduce environmental impact, and enhance production efficiency.

Industrial-scale feasibility for textile wastewater treatment via Photocatalysis-adsorption technology using black sand and UV lamp.

Dye-contaminated wastewater is a major environmental problem that requires effective and affordable treatment methods. This study investigates an innovative approach using black sand filtration assisted by UV light to remove methylene blue (MB) dye from wastewater. The motivation is to develop a sustainable low-cost wastewater treatment technology. Black sand's composition of iron oxide and other metal oxides enables the adsorption and photocatalytic degradation of dyes. The effects of operating parameters, including pH, bed height, flow rate, and initial MB concentration, were examined using a fixed-bed column system. The maximum adsorption capacity was 562.43 mg g-1 at optimal pH 10, 15 cm bed height, 50 ppm MB, and 53.33 mL min-1 flow rate. Mathematical models effectively described the experimental breakthrough curves. For real textile wastewater, black sand with a UV lamp removed 50.40% COD, 73.68% TDS, 43.82% TSS, and 98.57% conductivity, significantly outperforming filtration without UV assistance. Characterization via XRD, XRF, FTIR, zeta potential, and SEM revealed black sand's photocatalytic properties and mechanism of MB adsorption. The findings demonstrate black sand filtration plus UV irradiation as a feasible, sustainable technology for removing dyes and organics from wastewater. This method has promise for the scale-up treatment of textiles and other industrial effluents.

Correction to "Nanotechnology Impact on Chemical-Enhanced Oil Recovery: A Review and Bibliometric Analysis of Recent Developments".

[This corrects the article DOI: 10.1021/acsomega.3c06206.].

Emerald eco-synthesis: harnessing oleander for green silver nanoparticle production and advancing photocatalytic MB degradation with TiO2&CuO nanocomposite.

The tertiary composite of TiO2/CuO @ Ag (TCA) were synthesized by the solid state method using different ratios of TiO2/CuO NCs and Ag NPs. The structural, morphological, and optical properties of nanocomposites were analyzed by scanning electron microscope, Transmission electron microscope, X-ray diffraction, Fourier transform infrared spectra, UV-Vis diffuse reflectance spectra (UV-Vis/DRS) and photoluminescence spectrophotometry. The results showed enhanced activity of TCA hybrid nano crystals in oxidizing MB in water under visible light irradiation compared to pure TiO2. The photocatalytic performance TCA samples increased with suitable Ag content. The results show that the photo degradation efficiency of the TiO2 compound improved from 13 to 85% in the presence of TiO2-CuO and to 98.87% in the presence of Ag containing TiO2-CuO, which is 7.6 times higher than that of TiO2. Optical characterization results show enhanced nanocomposite absorption in the visible region with long lifetimes between e/h+ at optimal TiO2-CuO/Ag (TCA2) ratio. Reusable experiments indicated that the prepared TCA NC photo catalysts were stable during MB photo degradation and had practical applications for environmental remediation.

Flexible, durable, and anti-fouling maghemite copper oxide nanocomposite-based membrane with ultra-high flux and efficiency for oil-in-water emulsions separation.

In this study, we developed a novel nanocomposite-based membrane using maghemite copper oxide (MC) to enhance the separation efficiency of poly(vinyl chloride) (PVC) membranes for oil-in-water emulsions. The MC nanocomposite was synthesized using a co-precipitation method and incorporated into a PVC matrix by casting. The resulting nanocomposite-based membrane demonstrated a high degree of crystallinity and well-dispersed nanostructure, as confirmed by TEM, SEM, XRD, and FT-IR analyses. The performance of the membrane was evaluated in terms of water flux, solute rejection, and anti-fouling properties. The pinnacle of performance was unequivocally reached with a solution dosage of 50 mL, a solution concentration of 100 mg L-1, and a pump pressure of 2 bar, ensuring that every facet of the membrane's potential was fully harnessed. The new fabricated membrane exhibited superior efficiency for oil-water separation, with a rejection rate of 98% and an ultra-high flux of 0.102 L/m2 h compared to pure PVC membranes with about 90% rejection rate and an ultra-high flux of 0.085 L/m2 h. Furthermore, meticulous contact angle measurements revealed that the PMC nanocomposite membrane exhibited markedly lower contact angles (65° with water, 50° with ethanol, and 25° with hexane) compared to PVC membranes. This substantial reduction, transitioning from 85 to 65° with water, 65 to 50° with ethanol, and 45 to 25° with hexane for pure PVC membranes, underscores the profound enhancement in hydrophilicity attributed to the heightened nanoparticle content. Importantly, the rejection efficiency remained stable over five cycles, indicating excellent anti-fouling and cycling stability. The results highlight the potential of the maghemite copper oxide nanocomposite-based PVC membrane as a promising material for effective oil-in-water emulsion separation. This development opens up new possibilities for more flexible, durable, and anti-fouling membranes, making them ideal candidates for potential applications in separation technology. The presented findings provide valuable information for the advancement of membrane technology and its utilization in various industries, addressing the pressing challenge of oil-induced water pollution and promoting environmental sustainability.

Nanotechnology Impact on Chemical-Enhanced Oil Recovery: A Review and Bibliometric Analysis of Recent Developments.

Oil and gas are only two industries that could change because of nanotechnology, a rapidly growing field. The chemical-enhanced oil recovery (CEOR) method uses chemicals to accelerate oil flow from reservoirs. New and enhanced CEOR compounds that are more efficient and eco-friendly can be created using nanotechnology. One of the main research areas is creating novel nanomaterials that can transfer EOR chemicals to the reservoir more effectively. It was creating nanoparticles that can be used to change the viscosity and surface tension of reservoir fluids and constructing nanoparticles that can be utilized to improve the efficiency of the EOR compounds that are already in use. The assessment also identifies some difficulties that must be overcome before nanotechnology-based EOR can become widely used in industry. These difficulties include the requirement for creating mass-producible, cost-effective nanomaterials. There is a need to create strategies for supplying nanomaterials to the reservoir without endangering the formation of the reservoir. The requirement is to evaluate the environmental effects of CEOR compounds based on nanotechnology. The advantages of nanotechnology-based EOR are substantial despite the difficulties. Nanotechnology could make oil production more effective, profitable, and less environmentally harmful. An extensive overview of the most current advancements in nanotechnology-based EOR is provided in this paper. It is a useful resource for researchers and business people interested in this area. This review's analysis of current advancements in nanotechnology-based EOR shows that this area is attracting more and more attention. There have been a lot more publications on this subject in recent years, and a lot of research is being done on many facets of nanotechnology-based EOR. The scientometric investigation discovered serious inadequacies in earlier studies on adopting EOR and its potential benefits for a sustainable future. Research partnerships, joint ventures, and cutting-edge technology that consider assessing current changes and advances in oil output can all benefit from the results of our scientometric analysis.

Correction: Synthesis of novel solid scale inhibitors based on silver tungstate loaded KIT-6 for scale removal from produced water: static and modeling evaluation.

Correction for 'Synthesis of novel solid scale inhibitors based on silver tungstate loaded KIT-6 for scale removal from produced water: static and modeling evaluation' by Heba M. Salem, et al., Dalton Trans., 2023, https://doi.org/10.1039/d3dt02594b.

Synthesis of novel solid scale inhibitors based on silver tungstate loaded KIT-6 for scale removal from produced water: static and modeling evaluation.

Oilfield scaling is a major problem in the oil and gas industry. Scaling issues cost the industry millions of dollars in damage and lost production every year as scaling is one of the main causes of global production decline. In this study, solid scale inhibitors based on silver tungstate loaded KIT-6 were synthesized and evaluated using a static scale inhibition test. The synthesized materials were characterized using wide and low XRD, N2 adsorption-desorption, TGA, and FTIR, SEM, and XPS analyses. Small-angle XRD patterns showed that KIT-6 had 3D-mesopore diffraction peaks with a cubic Ia3d space group. Wide-angle XRD patterns of silver tungstate loaded KIT-6 confirmed the crystallinity. The prepared catalysts are characterized by higher surface areas (394-918 m2 g-1), large pore volumes (0.63-0.98 cm3 g-1), narrow pore size distributions (5.3 nm), and high thermal stability up to 1000 °C. The results of this study demonstrate that the inhibition efficiency of the scale inhibitor increases and that of the calcite scale inhibitor decreases with increasing pH (2 to 8). This proposes that the scale inhibitor is more effective under alkaline conditions. An inhibition efficiency of 99% on calcium carbonate can be achieved at an optimal dosage of 7.5 ppm at 55 °C, indicating that the scale inhibitor exhibits a relatively good inhibition performance on calcium carbonate. The use of these materials can potentially lead to more efficient and cost-effective solutions for scale inhibition in various industrial processes.

Efficient dye removal from industrial wastewater using sustainable activated carbon and its polyamide nanocomposite derived from agricultural and industrial wastes in column systems.

Sugar beet crown (SBC) waste was employed to produce sustainable activated carbon (AC) by a thermo-chemical activation procedure using a fixed ratio of H3PO4/SBC (1 : 1 w/w ratio) at 550 °C/2 h. An activated carbon/polyamide nano-composite (AC/PA) was also prepared through the polymerization of the fabricated AC (90%) with polyamide (PA, 10%) synthetic textile waste using a proper dissolving agent at a specified w/w ratio with the employed polymer (formic acid/PA = 82/18%). Both AC and its derivative AC/PA were employed in the remediation of dyes from industrial wastewater in column systems, and their efficiencies were compared at various applied experimental conditions. The adsorption of the industrial dye waste (IDW) was a pH-, flow rate-, and bed thickness-controlled process by the regarded adsorbents. Kinetic studies confirmed the suitability of the Thomas equation over the Yoon and Nelson model in predicting the dynamic adsorption process of IDW by AC and AC/PA as was assured by the close agreement among the calculated and experimental uptake capacities of both adsorbents at the same applied flow rates, suggesting the chemisorption nature of IDW adsorption. Additionally, electrostatic attraction was the leading mechanism of IDW adsorption by AC and AC/PA composite with some advantages of the former over the latter.

Removing of cationic dyes using self-cleaning membranes-based PVC/nano-cellulose combined with titanium aluminate.

This research used the phase inversion approach to construct polyvinyl chloride nanocellulose@titanium aluminate nanocomposite membranes (PVC/NC@TALCM) to adsorb and filter dye from wastewater. FTIR, XRD, and SEM were used to determine the adsorptive nanocomposite membrane that had been synthesized. The thermal and electrical properties measurements were carried out using a static system. The influence of several adsorbent dosages, pH, and dye concentrations on the nanocomposite membrane's adsorption ability was investigated. Using a dead-end filtration system, the PVC-NC@TALCM was evaluated as a pressure filtration membrane system. It was found that 98.6% of MB dye was removed by PVC-NC@TALCM membrane, which was loaded with 5% titanium aluminate at pH 10. The kinetic adsorption studies indicated that the adsorption of MB onto the PVC-NC@TALCM nanocomposite membrane obeys pseudo-second-order that indicates the chemosorption process. The isotherm data were described using Freundlich and Langmuir models, and the Freundlich isotherms were shown to be more closely match the experimental data than the Langmuir model. Finally, the PVC-NC@TALCM nanocomposite membrane was economical, environmentally friendly, and self-cleaning.

Synthetization and characterization of SnCaAl2O3 nanocomposite and using as a superior adsorbent for Pb, Zn, and Cd ions in polluted water.

The presence of heavy metals in drinking water or wastewater poses a serious threat to the ecosystem. Hence, the present study focused on synthesizing SnCaAl2O3 core-shell nanoparticles (C.N.P.s) in the α-Alumina phase by thermal annealing a stacked structure sandwiched between two Al2O3 layers at low temperatures. The obtained structure showed Sn N.P. floating gate with an Al2O3 dielectric stacked tunneling barrier to remove the excess of these heavy metals from polluted water. To characterize the prepared composites, X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), and high-resolution transmission electron microscopy (HR-TEM) were used. The synthesized SnCaAl2O3 C.N.P.s composite was examined to utilize it as an adsorbent for removing Zn, Cd, and Pb divalent cations. The removal efficiency was studied by various parameters such as adsorbent dose, pH, contact time, metal concentrations, temperature, and coexisting ions. The experimental results were tested via Langmuir and Freundlich isotherm models. The obtained results were convenient to the Freundlich isotherm model. Moreover, the adsorption thermodynamic behavior of Zn+2, Cd+2, and Pb+2 on the synthesized composite was examined, and the process is endothermic and spontaneous under experimental conditions. The results illustrated that the adsorption efficiency of the SnCaAl2O3 core-shell nanoparticles (C.N.P.s) ranged from 88% to about 100% for all cations.

Adsorption of Mn(ii) ions from wastewater using an AgNPs/GO/chitosan nanocomposite material.

Water contaminated with heavy metal ions is extremely poisonous and threatens living organisms. Therefore, scientists place a premium on removing heavy metal ions from water that has already been contaminated. Removing metal ions from water typically involves the use of nanomaterials. Chitosan was made by extracting it from shrimp shells and combining it with a 3 : 1 ratio of synthetically produced AgNPs/GO. Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) with transmission electron microscopy (TEM), and X-ray diffraction were used to investigate an AgNPs/GO/chitosan nanocomposite (XRD). A number of studies must be run to determine the optimal pH, adsorbent quantity, retention period, stirring speed, temperature, and initial concentration. The studies were conducted in a variety of ways. The isotherms of Langmuir, Freundlich, and Dubinin-Radushkevich were utilized. The industrial wastewater was used in the column adsorption experiment, and the flow rates and column bed heights were varied. An optimum contact time, pH, and adsorbent dosage for Mn(ii) were determined. At 30 minutes, pH 6, and 0.05 grams of Mn(ii) adsorbent per 100 ml, with agitation at 250 rpm, room temperature of 30 °C, and an initial concentration of 40 ppm, the best conditions were discovered. A positive correlation coefficient finding (R 2 = 0.925) indicates a good fit for Mn, according to equilibrium studies (II). The pseudo-second-order active model was connected to data that suited the pseudo-first and pseudo-second-order models. In the intra-particle diffusion model, the mechanism must proceed through four phases before equilibrium is reached. In an industrial adsorbent column, the adsorbent was put to the test. The periodicity test demonstrates that the nanocomposite's adsorption capability can be recovered by washing it with 0.1 M HCl. Mn(ii) adsorbed on AgNPs/GO/Chitosan after four cycles was only 20%, insufficient for additional adsorption tests. The repeated cycles that led to the partial loss of the adsorbate may have reduced the adsorbent material's efficacy.

Fe(iii) and Cr(vi) ions' removal using AgNPs/GO/chitosan nanocomposite as an adsorbent for wastewater treatment.

Heavy metal ions in water refer to significant risks to the biological system due to their high toxicity. Therefore, the decontamination of water polluted by heavy metal ions attracts significant interest of researchers. Adsorption by nanomaterials has been a widely used technique for removing heavy metal ions from water. Chitosan was extracted from shrimp shellfish and mixed with laboratory-prepared AgNPs/GO in the ratio of 3 : 1. A series of tests evaluates the best condition of pH, amount of adsorbent, retention time, stirring speed, temp, and initial concentration. The research was conducted under various conditions. Langmuir, Freundlich, Tempkin, and Dubinin-Radushkevich isotherms were also tested. Also, the column adsorption experiment was carried out on industrial wastewater at different flow rates and column bed heights. The optimal values of the contact time, pH, and adsorbent dose of Cr(vi) were found to be 80 min, 4, and 0.1 g 100 mL-1, respectively, at room temperature (30 °C), agitation at 150 rpm, and initial concentration of 50 ppm. On the other hand, the optimal value of contact time, pH, and adsorbent dose of Fe(iii) were found to be 30 min, 6, and 0.02 g 100 mL-1, respectively, at room temp (30 °C) with a stirring speed of 250 rpm and an initial concentration of 40 ppm. For Cr(vi) and Fe(iii), equilibrium studies show that the data fit the Freundlich isotherm well (correlation coefficient, R 2 = 0.98) (III). A link between the pseudo-second order active model and data fitting the pseudo-first order active models were made. Within the intraparticle diffusion model, there are four stages that the mechanism must go through before it is at equilibrium. The adsorbent was tested in an industrial adsorbent column. This test proves that the nanocomposite's adsorption capacity can be restored by washing it with 0.1 M HCl, as shown by the periodicity test. After four cycles, the amount of Cr(vi) adsorbed on AgNPs/GO/chitosan was just 20%, which is insufficient for further adsorption experiments. Cr(vi) removal rates (%R) decreased slightly.

Hybrid magnetic core-shell TiO2@CoFe3O4 composite towards visible light-driven photodegradation of Methylene blue dye and the heavy metal adsorption: isotherm and kinetic study.

Magnetic core-shell TiO2@CoFe3O4 (TCM) composite photocatalytic particles with a core-shell structure were synthesized by the co-precipitation method as a novel catalyst for methylene blue (MB) dye degradation and adsorption efficiency of heavy-metal ion Pb(II) from aqueous solution. Various analytical techniques have verified the formation of the TCM core-shell through TEM, XRD, FT-IR, Raman, PL, and UV analysis. The presence of TiO2 and cobalt magnetite in the TCM core shell is confirmed by XRD analysis. The formation of a homogenous CoFe3O4shell on TiO2 spheres is confirmed by HR-TEM investigation. TiO2 nanoparticle has a rutile structure with an average crystallite size of about 57.44 and a TCM core-shell of about 64.62 nm. From UV and PL studies, it was found that the core shell absorbs the visible range of the electromagnetic spectrum, which improves the effective separation between photo carriers. This study focused on several factors that influence metal ion adsorption, including initial concentrations, adsorbent dose, pH, and contact time. The TCM nanocomposite successfully separated the heavy metal ion Pb(II) from aqueous solutions, and the model predictions exactly matched the experimental results. For TCM material, the maximum adsorption efficiency for Pb(II) was 33.09 mg/g. The photocatalytic performance of TiO2 and TCM is about 12% and 91% after 60 min for MB dye degradation. It was found that TiO2@CoFe3O4 core-shell nanoparticles perform better as photo catalysts than pure TiO2 and CoFe3O4due to their high efficiency and reusability. Furthermore, the analysis revealed that heavy metal adsorption from aqueous solutions could be reused over seven cycles with no adsorption capacity modification.

Enhanced Nanofiltration Process of Thin Film Composite Membrane Using Dodecyl Phenol Ethoxylate and Oleic Acid Ethoxylate for Oilfield Calcite Scale Control.

This research studied the enhancing effect on the nanofiltration composite (TFCNF) membrane of two non-ionic surfactants on a thin-film composite nanofiltration membrane (TFCNF) for calcite scale (CaCO3) inhibition in oilfield application to develop a multifunctional filtration system: nanofiltration, antiscalant, and scale inhibitors. The effectiveness of dodecyl phenol ethoxylate (DPE) and oleic acid ethoxylate (OAE) as novel scale inhibitors were studied using the dynamic method. Scaling tests on the membrane were performed to measure the scaling of the inhibited membrane with and without scale inhibitors for salt rejection, permeability, and flux decline. The results revealed that the TFCNF membrane flux decline was improved in the presence of scale inhibitors from 22% to about 15%. The rejection of the membrane scales increases from 72% for blank membranes, reaching 97.2% and 88% for both DPE and OAE, respectively. These confirmed that scale inhibitor DPE had superior anti-scaling properties against calcite deposits on TFCNF membranes. Inhibited scaled TFCNF membrane was characterized using environmental scanning electron (ESEM), FTIR, and XRD techniques. The results of the prepared TFCNF membrane extensively scaled by the calcite deposits were correlated to its morphology.

Enhanced Performance of Chitosan via a Novel Quaternary Magnetic Nanocomposite Chitosan/Grafted Halloysitenanotubes@ZnγFe3O4 for Uptake of Cr (III), Fe (III), and Mn (II) from Wastewater.

A novel chitosan/grafted halloysitenanotubes@Znγmagnetite quaternary nanocomposite (Ch/g-HNTs@ZnγM) was fabricated using the chemical co-precipitation method to remove the ions of Cr (III), Fe (III), and Mn (II) from wastewater. The characteristics of the synthesized Ch/g-HNTs@ZnγM quaternary nanocomposite were investigated using FTIR, SEM, XRD, GPC, TGA, TEM, and surface zeta potential. The characterization analysis proved that the mentioned nanocomposite structure contains multiple functional groups with variable efficiencies. Additionally, they proved the existence of magnetic iron in the nanocomposite internal structure with the clarity of presentation of gaps and holes of high electron density on its surface. The results showed that the pH and time to reach an equilibrium system for all the studied metal ions were obtained at 9.0 and 60 min, respectively. The synthesized Ch/g-HNTs@ZnγM nanocomposite exhibited maximum adsorption removal of 95.2%, 99.06%, and 87.1% for Cr (III), Fe (III), and Mn (II) ions, respectively. The pseudo-second-order kinetic model and, for isotherm, the Langmuir model were best fitted with the experimental data. The thermodynamic parameters indicated the exothermic and spontaneous nature of the adsorption reaction as proven by the ΔH° and ΔG° values. Additionally, chemical adsorption by the coordination bond is supposed as the main mechanism of adsorption of the mentioned metal ions on the nanocomposite. Finally, Ch/g-HNTs@ZnγM displays prospected advantages, such as a low-expense adsorbent, high efficiency and availability, and an eco-friendly source, that will reduce the environmental load via an environmentally friendly method.