Effect of a Natural Surfactant (Fenugreek Seeds) on Emulsification and Mobilization of Paraffins via Pore-Scale Micromodel Experiments.

The surface characteristics of minerals have been crucial in predicting the interactions between chemicals, particularly in chemical flooding. Thus, this paper evaluates the viability of natural surfactants derived from agricultural products for oil recovery studies using a micromodel filled with paraffinic oil. The study investigates the interfacial tension, viscosity, microscopic, dilution, and oil mobilization characteristics of the natural surfactants. The experimental setup involves conducting interfacial tension measurements between the surfactant solution and paraffinic oil using the Wilhelmy plate method and was found to be 14.2, 10.92, and 9.8 mN/m. Additionally, viscosity measurements and frequency sweep analysis were performed to assess the rheological properties of the prepared emulsion, which was stabilized using a natural surfactant. Microscopic evaluation depicts that, among the prepared emulsions, n-heptane emulsion seems more stable at both 30 and 90 °C. Moreover, dilution studies were conducted for each emulsion system, and the dilution ratio was varied from 1:5 to 1:1 (emulsion/saline solution). It was found that n-heptane emulsion possesses better stability at higher dilution (until a 3:5 ratio). Oil mobilization studies are conducted using a glass micromodel to simulate reservoir conditions and observe the displacement efficiency of the surfactant solutions. The results indicate that natural surfactants exhibit competitive interfacial tension reduction and viscosity modification properties compared to commercial surfactants. Furthermore, oil mobilization studies demonstrate the effectiveness of natural surfactants in enhancing oil recovery from paraffinic oil reservoirs. These findings suggest the potential of natural surfactants derived from agricultural products as sustainable alternatives for improving the oil recovery efficiency in petroleum reservoirs.

Synthesis and Molecular Docking of some new Thiazolidinone and Thiadiazole Derivatives as Anticancer Agents.

New sets of functionalized thiazolidinone and thiadiazole derivatives were synthesized, and their cytotoxicity was evaluated on HepG2, MCF-7, HTC-116, and WI38 cells. The synthetic approach is based on the preparation of 4-(4-acetamidophenyl)thiosemicarbazide (4) and their thiosemicarbazones 5 a-e, which are converted to the corresponding thiazoldin-4-one compounds 6 a-e upon cyclization with ethyl bromoacetate. The thiadiazole compounds 9 and 12 were obtained by reacting 4-(4-acetamidophenyl)thiosemicarbazide with isothiocyanates and/or ethyl 2-cyano-3,3-bis(methylthio)acrylate, respectively. The thiazolidinone compounds 6 c and 6 e exhibited strong cytotoxicity against breast cancer cells, with an IC50 (6.70±0.5 µM) and IC50 (7.51±0.8 µM), respectively, very close to that of doxorubicin (IC50: 4.17±0.2 µM). In addition, the anti-cancer properties of the tested thiazolidinone and thiadiazole scaffolds were further explored by the molecular docking program (MOE)-(PDB Code-1DLS). Compounds 5 d, 5 e, 6 d, 6 e, and 7 have the best binding affinity, ranging from -8.5386 kcal.mol-1 to -8.2830 kcal.mol-1.

Synthesis of Some Novel Thiophene Analogues as Potential Anticancer Agents.

The aim of this study involves the synthesis novel thiophene analogues that can be used as anticancer medications through a strategic multicomponent reaction connecting ethyl 4-chloroacetoacetate (1), phenyl isothiocyanate, and a series of active methylene reagents, including ethyl acetoacetate (2), malononitrile, ethyl cyanoacetate, cyanoacetamide 6a-c, N-phenyl cyanoacetamide derivatives 13a-c, and acetoacetanilide derivatives 18. This reaction was facilitated by dry dimethylformamide with a catalytic quantity of K2CO3. The resultant thiophene derivatives were identified as 4, 8a-b, 9, 12a-d, 15a-c, and 20a-b. Further reaction of compound 4 with hydrazine hydrate yielded derivative 5, respectively. When compound 1 was refluxed with ethyl 3-mercapto-3-(phenylamino)-2-(p-substituted phenyldiazenyl)acrylate 10a-e in the presence of sodium ethoxide, it produced thiophene derivatives 12a-d. Comprehensive structural elucidation of these newly synthesized thiophene-analogues was accomplished via elemental and spectral analysis data. Furthermore, the study delves into the cytotoxicity of the newly synthesized thiophenes was evaluated using the HepG2, A2780, and A2780CP cell lines. The amino-thiophene derivative 15b exhibited an increased growth inhibition of A2780, and A2780CP with IC50 values 12±0.17, and 10±0.15 µM, respectively compared to Sorafenib with IC50 values 7.5±0.54 and 9.4±0.14. This research opens new avenues for developing thiophene-based anticancer agents.

Assessment of environmental pollution and human health risks of mine tailings in soil: after dam failure of the Córrego do Feijão Mine (in Brumadinho, Brazil).

The dam failure of the Córrego do Feijão Mine (CFM) located in Minas Gerais State, Brazil, killed at least 278 people. In addition, large extensions of aquatic and terrestrial ecosystems were destroyed, directly compromising the environmental and socioeconomic quality of the region. This study assessed the pollution and human health risks of soils impacted by the tailing spill of the CFM dam, along a sample perimeter of approximately 200 km. Based on potential ecological risk and pollution load indices, the enrichments of Cd, As, Hg, Cu, Pb and Ni in soils indicated that the Brumadinho, Mário Campos, Betim and São Joaquim de Bicas municipalities were the most affected areas by the broken dam. Restorative and reparative actions must be urgently carried out in these areas. For all contaminated areas, the children's group indicated an exacerbated propensity to the development of carcinogenic and non-carcinogenic diseases, mainly through the ingestion pathway. Toxicological risk assessments, including acute, chronic and genotoxic effects, on people living and working in mining areas should be a priority for public management and mining companies to ensure effective environmental measures that do not harm human health and well-being over time.

Influence of agricultural activities and seasonality on levels of selected physico-chemical parameters and heavy metals along River Yala in Lake Victoria Basin.

The aim of the work was to establish the effect of anthropogenic activities and seasonality on physico-chemical parameters and heavy metal levels of River Yala (RY) within RY Basin of Lake Victoria (LV), as well as the associated ecological risks. Analyses were done on the collected samples in order to establish the levels of EC, pH, DO, temperature, conductivity, turbidity, acidity, alkalinity, BOD, COD, DOC, TOC and heavy metals (Cu, Fe, Pb, Mn, Zn, Cr and Cd) in RY water and sediments adjacent to Agricultural Farms during dry and wet seasons. The levels in terms of µg/mL, µS/cm (EC), NTU (turbidity) of analyzed parameters in the Agricultural Farms in water ranged from 0.01±0.00 to 121.75±15.23 (Upstream pristine sources of RY - S), 0.02±0.01 to 184.83±23.43 (Nandi Tea Estate and Kaimosi Agricultural Farms - N), 0.02±0.01 to 149.67±22.77 (Subsistence Farms - Sub), 0.02±0.01 to 209.33±18.09 (Lake Agro Limited Agricutural Farms and Yala Swamp - D) and 0.01±0.00 to 164.25±30.33 (Terminal of RY - T). The levels in µg/g of analyzed parameters in sediments ranged from 7.2±1.46 to 3342.8±538.7 (S), 9.12±0.2 to 4063.2±90.4 (N), 3.15±1.14 to 5998.5±588.4 (Sub), 2.03±0.76 to 4519.8±194.9 (D) and 2.13±0.75 to 5514.4±201.4 (T). The significant differences in the levels of analyzed parameters in water between dry and wet seasons were computed as; EC (+20.54 µS/cm), alkalinity (-2.85 µg/mL), DOC (+0.24 µg/mL), Fe (+0.58 µg/mL), Pb (+0.11 µg/mL), Zn (+0.07 µg/mL) and Cd (+0.01 µg/mL) while that for Mn in sediment samples was +163.8937 µg/g. The significantly (p ≤ 0.05) positive values indicated that wet season had more impact on the levels than dry season. There was positive correlation of zinc in water and sediments during dry and wet season. Chromium correlated positively in water and sediments during wet season. Copper and cadmium correlated negatively during dry and wet season while Mn only wet season. Results of geostatistical indices (CF, Cd, mCd, PLI, Er and RI) indicated that sediments located at regions N, D and T were highly contaminated with the heavy metals. However, a wetland at the mouth of Lake Victoria cleaned the water before it drained into the lake. Therefore, despite contamination of RY through anthropogenic activities, wetland mitigation protects LV from pollution by the river, indicating the important ecological and restorative functions played by wetlands.

Fabrication of magnetite nanomaterials employing novel ionic liquids for efficient oil spill cleanup.

The oil spill represents one of the most important pollution sources for marine environments, that occurs due to tanker collisions, ship accidents, and platforms. Several techniques are used for treating oil spill disasters including chemical, physical, and biochemical. The use of chemicals, magnetite nanomaterials (MNMs) in particular, is one of the most applied techniques used for oil spill remediation due to their low cost, fast remediation, and reusability. This work aims to synthesize and use new ionic liquids (ILs) for the modification of MNMs surfaces to enhance their performance for crude oil uptake. For that, octadecylamine (OA) was reacted with epichlorohydrin (EH), followed by reaction with either diethylenetriamine (DT), or tetraethylenepentamine (TP) to obtain corresponding amines, OADT, and OATP, respectively. The produced amines were quaternized using acetic acid (AA) forming corresponding ILs, OADT-IL, and OATP-IL. The obtained ILs, OADT-IL, and OATP-IL were applied for modification of magnetite nanomaterials (MNMs) surface to obtain the surface-modified MNMs, DT-MNMs, and TP-MNMs, respectively. The surface-modified MNMs were characterized using different techniques including Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), vibrating sample magnetometer (VSM), and contact angle. The efficacy of DT-MNMs, and TP-MNMs for heavy crude oil uptake (EMU) was evaluated. Further, the factors affecting on the crude oil uptake including MNMs: heavy crude oil ratio, and contact time were also evaluated. The data exhibited that, the EMU relatively declined as the ratio of DT-MNMs, and TP-MNMs decreased. Even at low MNMs:crude oil ratio (1:50), DT-MNMs, and TP-MNMs displayed EMU 87%, and 90%, respectively, which means 1 g of either DT-MNMs, or TP-MNMs can uptake 45 g, or 43.5 g, respectively. These values are high as compared with other studies that reported the use of MNMs for oil spill cleanup. Furthermore, the data indicated that the EMU increased as the contact time increased, and reached maximum EMU of 98% for both MNMs samples after 10 min.

New Amphiphilic Ionic Liquids for the Demulsification of Water-in-Heavy Crude Oil Emulsion.

This work aimed to use abietic acid (AA), as a widely available natural product, as a precursor for the synthesis of two new amphiphilic ionic liquids (AILs) and apply them as effective demulsifiers for water-in-crude oil (W/O) emulsions. AA was esterified using tetraethylene glycol (TEG) in the presence of p-toluene sulfonic acid (PTSA) as a catalyst obtaining the corresponding ester (AATG). AATG was reacted with 1-vinylimidazole (VIM) throughout the Diels-Alder reaction, forming the corresponding adduct (ATI). Following this, ATI was quaternized using alkyl iodides, ethyl iodide (EI), and hexyl iodide (HI) to obtain the corresponding AILs, ATEI-IL, and ATHI-IL, respectively. The chemical structure, surface activity, thermal stability, and relative solubility number (RSN) were investigated using different techniques. The efficiency of ATEI-IL and ATHI-IL to demulsify W/O emulsions in different crude oil: brine volumetric ratios were evaluated. ATEI-IL and ATHI-IL achieved promising results as demulsifiers. Their demulsification efficiency increased as the brine ratios decreased where their efficiency reached 100% at the crude oil: brine ratio (90:10), even at low concentrations.

Novel Bio-Based Amphiphilic Ionic Liquids for the Efficient Demulsification of Heavy Crude Oil Emulsions.

In the last few decades, there has been an increasing trend for the usage of natural products and their derivatives as green and renewable oil-filed chemicals. Use of these compounds or their derivatives contributes to reducing the use of traditional chemicals, and enhances green chemistry principles. Curcumin (CRC) is one of the most popular natural products and is widely available. The green character, antioxidant action, and low cost of CRC prompt its use in several applications. In the present study, Curcumin was used to synthesize two new amphiphilic ionic liquids (AILs) by reacting with 1,3-propanesultone or bromoacetic acid to produce corresponding sulfonic and carboxylic acids, CRC-PS and CRC-BA, respectively. Following this, the formed CRC-PS and CRC-BA were allowed to react with 12-(2-hydroxyethyl)-15-(4-nonylphenoxy)-3,6,9-trioxa-12-azapentadecane-1,14-diol (HNTA) to form corresponding AILs, GCP-IL and GRB-IL, respectively. The chemical structures, surface tension, interfacial tension, and relative solubility number (RSN) of the synthesized AILs were investigated. The efficiency of GCP-IL and GRB-IL to demulsify water in heavy crude oil (W/O) emulsions was also investigated, where we observed that both GCP-IL and GRB-IL served as high-efficiency demulsifiers and the efficiency increased with a decreased ratio of water in W/O emulsion. Moreover, the data showed an increased efficiency of these AILs with an increased concentration. Among the two AILs, under testing conditions, GCP-IL exhibited a higher efficiency, shorter demulsification time, and cleaner demulsified water.

Fabrication of New Demulsifiers Employing the Waste Polyethylene Terephthalate and their Demulsification Efficiency for Heavy Crude Oil Emulsions.

Two novel amphiphilic polyethylene amine terephthalate have been prepared via the glycolsis of polyethylene terephthalate (PET). The product, bis (2-hydroxyethyl terephthalate) (BHET), was converted to the corresponding dialkyl halide, bis(2-chloroethyl) terephthalate (BCET), using thionyl chloride (TC). This dialkyl compound was used for alkylation of dodecyl amine (DOA) and tetraethylenepentamine (TEPA) or pentaethylenehexamine (PEHA) to form the corresponding polyethylene amine terephthalate, i.e., DOAT and DOAP, respectively. Their chemical structure, surface tension, interfacial tension (IFT), and dynamic light scattering (DLS) were determined using different techniques. The efficiency of the prepared polyethylene amine terephthalate to demulsify water in heavy crude (W/O) emulsions was also determined and found to increase as their concentrations increased. Moreover, DOAT showed faster and higher efficiency, and cleaner separation than DOAP.

Hybrid Ionic Silver and Magnetite Microgels Nanocomposites for Efficient Removal of Methylene Blue.

The ionic crosslinked 2-acrylamido-2-methylpropane sulfonic acid-co-acrylic acid hydrogel, AMPS/AA and its Ag and Fe3O4 composites were synthesized using an in situ technique. The surface charge, particle sizes, morphology, and thermal stability of the prepared AMPS/AA-Ag and AMPS/AA-Fe3O4 composites were evaluated using different analytical techniques and their adsorption characteristics were evaluated to remove the methylene blue cationic dye, MB, from their aqueous solutions at optimum conditions. Also, the same monomers were used to synthesize AMPS/AA microgel and its Ag and Fe3O4 nanocomposites, which were synthesized using the same technique. The AMPS/AA-Fe3O4 nanocomposite was selected as conventional iron-supported catalyst due to the presence of both Fe(II) and Fe(III) species besides its magnetic properties that allow their easy, fast, and inexpensive separation from the aqueous solution. It was then evaluated as a heterogeneous catalyst for complete MB degradation from aqueous solution by heterogeneous Fenton oxidation. It achieved a high rate of degradation, degrading 100 mg L-1 of MB during a short time of 35 min as compared with the reported literature.

Facile fabrication of magnetite nanoparticles with new hydrophobic amides and their application in oil spill remediation.

In this study, inexpensive magnetite nanoparticles (Fe3O4) were prepared and applied to oil spill remediation. To do so, two novel hydrophobic amides, HADN and HATN, were prepared and applied to Fe3O4 surface modification, producing HAN-Fe3O4 and HAT-Fe3O4, respectively. The efficiency of HAN-Fe3O4 and HAT-Fe3O4 for oil spill remediation (EOSR) was investigated using different HAN-Fe3O4 and HAT-Fe3O4 weights and at various contact times. The data indicated that the EOSR increased with increased HAN-Fe3O4 and HAT-Fe3O4 weights, as their EOSR reached 100% and 89%, respectively, using 100 mg. The results also revealed that the optimum time for HAN-Fe3O4 and HAT-Fe3O4 (50 mg) to achieve the highest EOSR is 8 min, as their EOSR reached 98% and 84%, respectively, at this time. In addition, HAN-Fe3O4 exhibited higher EOSR than HAT-Fe3O4, which could be linked to the presence of an aromatic ring in HADN that is used for surface modification of Fe3O4, making them more compatible with crude oil components.

One-Pot Synthesis of Amphipathic Esters for Demulsification of Water-in-Crude Oil Emulsions.

The current work aims to synthesize new amphipathic compounds, TGHA and PGHA, and investigate their demulsification performance (DP) in water-in-crude oil emulsions. Their chemical structures, thermal stability, interfacial activity, and micelle formation were investigated by different techniques. The bottle test method was used to investigate the effect of demulsifier concentration, water content, temperature, and demulsification time (DT) on the DP of TGHA and PGHA compared to a commercial demulsifier (CD). The results indicated that these parameters have a noticeable impact on the DP of TGHA and PGHA. The results also showed that TGHA exhibited higher DP than PGHA at all investigated parameters, which could be explained by increasing its hydrophobicity due to lower oxyethylene units in its structure than PGHA. An increase in these units means increased hydrophilicity, which led to obstruction of PGHA molecule diffusion in crude oil as a continuous phase. Moreover, TGHA gave a comparable DP with CD, as it gave a higher DP and shorter DT than CD at a higher water content (50%), while the latter achieved the highest DP and the shortest DT at a low water content (10%).

Efficient Demulsification of Crude Oil Emulsion Using Novel Sugar-based Surfactant.

This study aimed to synthesize ecofriendly and low-cost surfactant-based sugar, HA-ST, under mild conditions and a short route via an opening ring of hexadecylsuccinic anhydride (HA) using starch (ST). HA-ST's chemical structure, thermal behavior, and surface activity were evaluated using Fourier Transform Infrared (FTIR) spectroscopy, thermogravimetric analysis, and a pendant drop technique. The results indicated HA-ST formation, thermal stability, and surface activity. HA-ST's green character, low cost, and surface activity recommended its use as a demulsifier for crude oil emulsions at different affecting parameters such as temperature, seawater ratio (SR), demulsifier concentration, demulsification time (DT), and pH. HA-ST demulsification efficiency (DE) was evaluated and compared with a commercial demulsifier (CD). The results showed improved HA-ST's DE with rising temperature, SR, demulsifier concentration, DT, and pH. The DE of HAST reached 100% at 50% of SR and 250 ppm of demulsifier concentration; the same results were obtained using CD. In contrast, HA-ST gave relatively lower DE at low SR (10%) with a value of 70% than the obtained using CD with a value of 75%. The green character, low cost, and DE of HA-ST make it suitable for demulsifying crude oil emulsions, especially those containing more than 30% seawater, compared with CD, which commonly contains two or more traditional surfactants.

Extracting and characterizing novel cellulose fibers from Chamaerops humilis rachis for textiles' sustainable and cleaner production as reinforcement for potential applications.

New cellulose (CL) fibers are derived from Chamaerops humilis (Ch) rachis. They play an essential role in various industries to produce environmentally friendly products as an alternative to enhancing and strengthening lightweight composites, such as dashboards automotive. Distinctive properties of Ch fibers (ChFs) were determined by extracting fibers from dwarf palm plant branches using anaerobic analysis. This search comprehensively studies morphological, physical, mechanical, and thermal characteristics and water absorption testing. The fiber diameter was 241.23 ± 34.77 µm, while the obtained linear density and density were 13.71 ± 0.57 Tex and 0.801 ± 0.05 g/cm3, respectively. The moisture content was 8.5 %, and the moisture regain was 9.29 %. Scanning electron microscopy images showed the fibers and smooth and rough surfaces. The thermogravimetric analysis demonstrated the maximum degradation of 352 °C, thermal stability of 243 °C, and the kinetic activation energy reached (79.78 kJ/mol). X-ray diffraction proves the availability of CL, with a crystallinity index = 68.38 % and crystal size = 2.92 nm. Fourier transform infrared succeeded in detecting functional groups and chemical compounds of fibers. The fibers exhibited a tensile stress of 110.85 ± 77.08 MPa, an elongation at a break rate of 2.29 ± 1.27 %, and Young's modulus of 6.05 ± 3.9 GPa. The maximum likelihood method (2P-Weibull distribution) was employed to examine the distribution of mechanical properties of fibers. According to the results above, new ChFs are an excellent reinforcement for elaborating fiber-reinforced biocomposites.

Improved Synthesis of Cu2O NPs and Ascorbic Acid-Modified Derivatives for Adsorption of Brilliant Cresyl Blue: Surface and Reusability Studies.

This study addresses the critical need for efficient and recyclable photocatalysts for water treatment applications by presenting a novel approach for the synthesis and characterization of copper (I) oxide (Cu2O) nanoparticles modified with ascorbic acid (Cu2O/AA). The motivation for this research stems from the increasing concern about environmental pollution caused by organic pollutants, such as Brilliant Cresyl Blue (BCB), and the necessity for sustainable solutions to mitigate this issue. Through comprehensive characterization techniques including Ultraviolet-Visible spectroscopy (UV-Vis), Fourier Transform Infrared spectroscopy (FTIR), X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), zeta potential measurements, and Brunauer-Emmett-Teller (BET) analysis, we demonstrate a significant modification to the electronic structure, enhancing the photocatalytic activity of Cu2O/AA. BET analysis revealed a mesoporous structure with a specific surface area of 2.7247 m2/g for Cu2O/AA, further emphasizing its potential for enhanced catalytic performance. The photocatalytic degradation studies showcased remarkable efficiency improvements, with degradation coefficients of 30.8% and 73.12% for Cu2O NPs and Cu2O/AA NC, respectively, within a 120 min timeframe. Additionally, recyclability experiments indicated sustained efficiency over five consecutive cycles, with both catalysts retaining crystalline integrity. These findings underscore the promising potential of Cu2O/AA nanoparticles as highly efficient and recyclable photocatalysts for the degradation of organic pollutants, offering superior performance compared to pure Cu2O NPs and addressing the pressing need for sustainable water treatment solutions.

Characterization optimization of synthesis Chitosanclay/benzoin/Fe3O4 composite for adsorption of Thionine dye by design expert study.

A novel composite material, magnetic chitosan-clay/benzoin/Fe3O4 (CS-CY/Benz/Fe3O4), was synthesized for effectively removing thionine dye (TH) from water solutions. The structural integrity and suitability of CS- CY/Benz/Fe3O4 composite for adsorption purposes were validated through extensive characterization techniques including BET, XRD, FTIR, and SEM. The adsorption efficiency was optimized through a Box-Behnken design (BBD) employing response surface methodology (RSM), focusing on variables such as adsorbent dose (A: 0.02-0.08 g), solution pH (B: 4-10), temperature (C: 30-60 °C), and time (D: 5-30 min). Experimental results revealed a maximum TH removal of 99% with significant interactions between temperature (C) and time (D) (p-value = 0.0001). The optimal conditions for TH removal were determined as pH ~ 5.91, adsorbent dosage of 0.08 g, temperature of 54.34 °C, and time of 29.7 min. The investigation of kinetics revealed that the adsorption process conformed to a pseudo-second-order (PSO) model, while the equilibrium data were effectively described by the Freundlich isotherm model. At a temperature of 333.15 K and a TH concentration of 350 mg/L, the adsorption capacity was determined to be 660.86 mg/g. The mechanism of adsorption encompassed various interactions such as electrostatic attractions, n-π interactions, hydrogen bonding, and Yoshida H-bonding. Particularly, the CS-CY/Benz/Fe3O4 composite demonstrated strong magnetic responsiveness, enabling straightforward separation from water using an external magnetic field after adsorption. Particularly, the CS-CY/Benz/Fe3O4 composite demonstrated strong magnetic responsiveness, enabling straightforward separation from water using an external magnetic field after adsorption. This research contributes important findings to the advancement of magnetic chitosan-based composites for efficient removal of TH dye pollutants from water environments.

Fabrication of Supported and Unsupported Gold Nanorods for Nonenzymatic Glucose Sensing and Study of Their Growth Kinetics.

This work includes a novel approach for synthesis/fabrication of AuNRs of varied aspect ratios leading to investigation on the kinetics of their growth mechanism. The synthesized AuNRs were further functionalized with MWCNTs (AuNRs@MWCNTs) by one-pot synthesis. The synthesized AuNRs and AuNRs@MWCNTs were characterized by employing UV-vis spectroscopy. Red shifts in the spectra of AuNRs confirmed the formation of nanorods of higher aspect ratios. Morphology of AuNRs and functionalized AuNRs was confirmed by high-resolution scanning electron microscopy. Biological studies were carried out by fabricating efficient nonenzymatic glucose sensors for optical and electrochemical sensing via UV and cyclic voltammetry in the detection ranges of 0.7-28 mM glucose (UV) and 5.5 µM-0.33 mM (CV). An electrochemical sensing study was carried out via AuNR- and AuNRs@MWCNT-modified GCEs in a 0.1 M NaOH electrolyte solution. The modified electrodes exhibited very high sensitivity with a broad linear range. The order of sensitivity (via CV) was found to be AuNRX0@MWCNTs > AuNRD5@MWCNTs > AuNRD5 > AuNRX0.

Synthesis and Performance of Two New Amphiphilic Ionic Liquids for Demulsification of Water-in-Crude Oil Emulsions.

This work aims to synthesize and apply two novel amphiphilic ionic liquids (AILs) for the demulsification of water-in-crude oil (W/O) emulsions. To do that, 4-tetradecylaniline (TA) and 4-hexylamine (HA) were etherified using tetrethylene glycol (TEG) in the presence of bis(2- chloroethoxyethyl)ether (BE) as a cross-linker, yielding corresponding ethoxylated amines TTB and HTB. The obtained ethoxylated amines TTB and HTB were quaternized with acetic acid (AA), obtaining corresponding AILs TTB-AA and HTB-AA. The chemical structures, surface tension (ST), interfacial tension (IFT), and micelle size were investigated with various techniques. The performance of TTB-AA and HTB-AA to demulsify W/O emulsions was investigated using different influencing factors, including the demulsifier concentration, water content, salinity, and pH. Additionally, the obtained results were compared with a commercial demulsifier. The results indicated that the demulsification performance (DP) increased as the demulsifier concentration increased and the water content decreased; however, increased salinity slightly improved the DP. The data also showed that the highest DPs were achieved at a pH of 7, which suggested a change in the chemical structure of these AILs at a lower and higher pH due to their ionic structure. Furthermore, TTB-AA demonstrated higher DP than HTB-AA, which could be explained by its higher ability to reduce IFT due to a longer alkyl chain than that of HTB-AA. Furthermore, TTB-AA and HTB-AA showed significant DP compared to the commercial demulsifier especially with W/O emulsions at low water content.

Surface-modified magnetite nanoparticles using polyethylene terephthalate waste derivatives for oil spill remediation.

This work aims at synthesizing new cross-linked poly ionic liquids, CPILs, VIMDE-Cl and CPIL, VIMDE-TFA, utilizing polyethylene terephthalate waste as a precursor and applying them to magnetite nanoparticles surface modification, producing surface-modified magnetite nanoparticles, SMNPs, VDCL/MNPs, and VDTA/MNPs, respectively. The structures of VIMDE-Cl and VIMDE-TFA, VDCL/MNPs, and VDTA/MNPs, were verified using different techniques. The particle sizes of SMNPs, VDCL/MNPs, and VDTA/MNPs, were evaluated with a transmission electron microscope and dynamic light scattering. The compatibility of VDCL/MNPs and VDTA/MNPs with crude oil components and their response to an external magnet were also measured using contact angle measurements and a vibrating sample magnetometer. The data confirmed the formation of SMNPs, nanosized structure, compatibility with oil components, and response to an external magnet. For that, VDCL/MNPs and VDTA/MNPs were applied for oil spill recovery using different SMNP : crude oil weight ratios. The impact of contact time on SMNPs' performance was also evaluated. The data indicated increased performance with an increase in SMNPs ratio, reaching maximum values of 99% and 96% for VDCL/MNPs and VDTA/MNPs, respectively, at SMNPs : crude oil ratio of 1 : 1. According to the results, the optimal contact time was 6 min, resulting in 89% and 97% performance for VDCL/MNPs and VDTA/MNPs at 1 : 4 SMNPs : crude oil ratio.

Efficient Oil Spill Uptake Using Surface-Modified Magnetite Nanoparticles with PET Waste Derivatives.

This work deals with poly(ethylene terephthalate) waste as a precursor to synthesize new cross-linked poly(ionic liquids) (CLPILs). The newly synthesized CLPILs, VPCT-Cl and VPCT-AA, were used for magnetite nanoparticle surface modification, producing VCL/Fe3O4 and VAA/Fe3O4, respectively. The chemical structures of the CLPILs and surface-modified Fe3O4 were elucidated by Fourier transform infrared and X-ray diffraction. Additionally, the particle size, zeta potential (ζ), contact angle, and magnetic properties of VCL/Fe3O4 and VAA/Fe3O4 were investigated using different techniques. Furthermore, the performance of these nanoparticles for oil spill cleanup was evaluated using various influencing factors, e.g., the contact time and the Fe3O4/crude oil ratio. VCL/Fe3O4 and VAA/Fe3O4 showed excellent performance in oil spill cleanup. The data showed that the performance increased with the contact time and the Fe3O4 ratio. Furthermore, the reusability of VCL/Fe3O4 and VAA/Fe3O4 over four cycles was also explored. The reusability data indicated that reused VCL/Fe3O4 and VAA/Fe3O4 showed promising performance in oil spill cleanup.