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This study aims to investigate the potential of integrating natural biochar (BC) derived from eggshell waste into flexible polyurethane (FPU) foam to enhance its mechanical and acoustic performance. The study explores the impact of incorporating BC at various weight ratios (0.1, 0.3, 0.5, and 0.7 wt. %) on the properties of the FPU foam. Additionally, the effects of modifying the BC with (3-aminopropyl)trimethoxysilane (APTMS) at different ratios (10, 20, and 30 wt. %) and the influence of diverse particle sizes of BC on the thermal, mechanical, and acoustic characteristics of the FPU composite are investigated. The functional groups, morphology, and elemental composition of the developed FPU composites are analyzed using Fourier-transform infrared spectroscopy (FTIR), field-emission scanning electron microscopy (FESEM), and energy-dispersive X-ray (EDX) techniques. Characteristics such as density, gel fraction, and porosity were also assessed. The results reveal that the density of FPU foam increased by 4.32% and 7.83% while the porosity decreased to 50.22% and 47.05% with the addition of 0.1 wt. % of unmodified BC and modified BC with 20 wt. % APTMS, respectively, compared to unfilled FPU. Additionally, the gel fraction of the FPU matrix increases by 1.91% and 3.55% with the inclusion of 0.1 wt. % unmodified BC and modified BC with 20 wt. % APTMS, respectively. Furthermore, TGA analysis revealed that all FPU composites demonstrate improved thermal stability compared to unfilled FPU, reaching a peak value of 312.17°C for the FPU sample incorporating BC modified with 20 wt. % APTMS. Compression strength increased with 0.1 wt. % untreated BC but decreased at higher concentrations. Modifying BC with 20% APTMS resulted in an 8.23% increase in compressive strength compared to unfilled FPU. Acoustic analysis showed that the addition of BC improved absorption, and modified BC enhanced absorption characteristics of FPU, reaching Class D with a 20 mm thickness. BC modified with APTMS further improved acoustic properties compared to the unfilled FPU sample (Class E), with 20% modification showing the best results. These composites present promising materials for sound absorption applications and address environmental issues related to eggshell waste., (© 2024. The Author(s).)

Uncontrolled or improperly managed wastewater is considered toxic and dangerous to plants, animals, and people, as well as negatively impacting the ecosystem. In this research, the use of we aimed to prepare polymer nanocomposites (guar gum/polyvinyl alcohol, and nano-montmorillonite clay) for eliminating heavy metals from water-based systems, especially Cu 2+ and Cd 2+ ions. The synthesis of nanocomposites was done by the green method with different ratios of guar gum to PVA (50/50), (60/40), and (80/20) wt%, in addition to glycerol that acts as a cross-linker. Fourier-transform infrared spectroscopy (FT-IR) analysis of the prepared (guar gum/PVA/MMT) polymeric nano-composites' structure and morphology revealed the presence of both guar gum and PVA's functional groups in the polymeric network matrix. Transmission electron microscopy (TEM) analysis was also performed, which verified the creation of a nanocomposite. Furthermore, theromgravimetric analysis (TGA) demonstrated the biocomposites' excellent thermal properties. For those metal ions, the extreme uptake was found at pH 6.0 in each instance. The Equilibrium uptake capacities of the three prepared nanocomposites were achieved within 240 min. The maximal capacities were found to be 95, 89 and 84 mg/g for Cu 2+ , and for Cd 2+ were found to be 100, 91, 87 mg/g for guar gum (80/20, 60/40 and 50/50), respectively. The pseudo-2 nd -order model with R 2 > 0.98 was demonstrated to be followed by the adsorption reaction, according to the presented results. In less than 4 hours, the adsorption equilibrium was reached. Furthermore, a 1% EDTA solution could be used to revitalize the metal-ion-loaded nanocomposites for several cycles. The most promising nanocomposite with efficiency above 90% for the removal of Cu 2+ and Cd 2+ ions from wastewater was found to have a guar (80/20) weight percentage, according to the results obtained., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2024 Alhaithloul, Alsudays, Zaki, Elsaeed, Mubark, Salib, Safwat, Niedbała, Diab, Abdein, Alharthi, Zakai and Elkelish.)

Recently, the scientific community's main goal is the long-term sustainability. Vegetable oils are easily accessible, non-depletable, and cost-effective materials. Vegetable oils are used to prepare polymeric alkyd surfaces. Novel and exciting designs of alkyd/graphene nanocomposites have provided eco-friendly thermal stability and protective coating surfaces. This review has briefly described important graphene-based alkyd nanocomposites along with their applications as protective coatings. These alkyd composites have high hydrophobicity, corrosion resistance, and durability. Graphene-based alkyd nanocoatings have many industrial and research interests because of their exceptional thermal and chemical properties. This work introduces an advanced horizon for developing protective nanocomposite coatings. The anti-corrosion properties and coatings' longevity may be improved by combining the synergistic effects of hybrid nanofillers introduced in this work., (© 2024. The Author(s).)

A novel series of polymeric ionic liquids (ILs) based on benzimidazolium chloride derivatives, namely, 1,3-diheptyl-2-(2-phenyl-propyl)-3 H -benzimidazol-1-ium chloride (IL1), 1,3-dioctyl-2-(2-phenyl-propyl)-3 H -benzimidazol-1-ium chloride (IL2), and 1,3-Bis-decyl-2-(2-phenyl-propyl)-3 H -benzoimidazol-1-ium chloride (IL3), were synthesized and chemically elucidated by Fourier transform infrared spectroscopy, 1 H NMR, 13 C NMR, and elemental analysis. Their influence as corrosion suppressors were investigated for C-steel corrosion in 1 M HCl, by weight loss (WL), potentiodynamic polarization (PDP), and electrochemical impedance spectroscopy (EIS) methods, revealing that their exclusive addition decreased corrosion with mounting concentrations. These assays demonstrated that novel ILs are efficient inhibitors at relatively low dosages. The efficacy of the synthesized ILs reached 79.7, 92.2 and 96.9%, respectively, at 250 ppm and 303 K. Parameters for activation and adsorption were calculated and are discussed. The Tafel polarization results demonstrated that the investigated ILs support the suppression of both cathodic and anodic reactions, acting as mixed type inhibitors. Langmuir's adsorption isotherm was confirmed as the best fitted isotherm, describing the physical-chemical adsorption capability of used ILs on the C-steel surface with the change in the free energy of adsorption, Δ G ° ads = 32.6-37.2 kJ mol -1 . The efficacy of the synthesized ILs was improved by increasing the doses, and the temperature reached 86.6, 96.1, and 98.4%, respectively, at 318 K. Surface morphology was proved by Fourier Transform Infrared spectroscopy, X-ray photoelectron spectroscopy, and atomic force microscopy (AFM), and then, changes in test solutions were checked by Ultraviolet-visible spectroscopy. Theoretical modeling (density functional theory and Monte Carlo) revealed the correlation between the IL's molecular chemical structure and its anticorrosive property., Competing Interests: The authors declare no competing financial interest., (© 2023 The Authors. Published by American Chemical Society.)

The hazards of polymer waste and emitted gas on the environment pose a global challenge. As a trial to control this, the current work aims to reuse the polymer waste mix (PM) as fillers in calcium silicate to prepare new composites of environmentally friendly polymer concrete. PM was first subjected to treatment to obtain treated PM (TPM) and then was filled in new dicalcium silicate cement with different concentrations. The microstructural characterizations declare the successful preparation of the dicalcium silicate base material. After the curing reaction, the precipitated carbonate main product is responsible for the gained properties. The CO 2 uptake% in the proposed composites reached 16.6%, referring to the successful storage of CO 2 gas during curing. The treatment reaction led to an increase in the flexural and compression strengths due to the strengthening of the polymer waste mix-cement interface; the strengths were increased gradually with more contents of TPM fillers. 7% TPM-cement concentration achieved the highest flexural strength and compression strength of10.2 and 12.7%, respectively, compared with blank cement. The used polymer improved slightly the pull-off force of the prepared cement, and 7 and 5% TPM-cement composites have the maximum values. All the proposed composites passed the impact testing without failure, where the combination between the polymer waste and silicate cement resulted in a stable composite surface. Compared with the blank, the different concentrations of TPM-cement composites show more stability against water absorption. In addition, the proposed composites and blank cement have a very low carbon dioxide emission. The ability to recycle the polymer waste, form new type of low-energy silicate, improve the mechanical and surface properties, uptake CO 2 gas, and reduce gas emission makes the proposed polymer waste mix-cement composites as environmentally friendly construction products., Competing Interests: The authors declare no competing financial interest., (© 2023 The Authors. Published by American Chemical Society.)

Over time, oil consumption has increased along with a continuous demand for petroleum products that require finding ways to increase hydrocarbon production more economically and effectively. So, enhanced oil recovery technologies are believed to be very promising and will serve as a key to meeting the future energy demand. This paper aims to introduce an innovative method to boost the EOR by using two novel types of surfactants synthesized from sulfonamide derivatives. Types I and II surfactants were analyzed using Fourier transform infrared spectroscopy, and their characterization was further performed using 1 H NMR and 13 C NMR spectroscopy. Additionally, the evaluation of these surfactants included interfacial tension measurements at concentrations up to 0.9 wt %. The combination of types I and II surfactants with alkaline (NaOH) was also investigated by the measurements of interfacial tension. A series of coreflood and sandpack tests under high-salinity conditions were carried out to assess the effects of a surfactant alone and alkaline-surfactant as a combination on improving oil recovery. The rock wettability was evaluated using relative permeability saturation curves, and the oil displacement efficiency was determined using fractional flow curves. The coreflood results demonstrated that alkaline-surfactant flooding with the chemical formula 0.2 wt % surfactant type II plus 0.5 wt % NaOH achieved a higher oil recovery of 74% OOIP compared to surfactant flooding with the chemical formula 0.5 wt % surfactant type II (64% OOIP) and waterflooding (saline solution with a 35,000 ppm salinity: 48% OOIP). Moreover, the experimental results showed that under both core and sandpack flood conditions, there was a noticeable reduction in oil-water interfacial tension, a change in rock wettability to more water-wet, and higher efficiency of oil displacement when alkaline was added to the surfactant. Based on current research, the alkaline-surfactant formulation is strongly recommended for chemical flooding because of its high efficacy and relatively low cost., Competing Interests: The authors declare no competing financial interest., (© 2023 The Authors. Published by American Chemical Society.)

Hydrogel membranes are prepared by casting a mixture of gellan gum (associated with PVA) and biochar produced from a local Egyptian plant. The mesoporous material is characterized by a specific surface area close to 134 m 2 g -1 , a residue of 28 % (at 800 °C), and a pH PZC close to 6.43. After grinding, the material is tested for Methylene Blue sorption at pH 10.5: sorption capacity reaches 1.70 mmol MB g -1 (synergistic effect of the precursors). The sorption isotherms are fitted by both Langmuir and Sips eqs. MB sorption increases with temperature: the sorption is endothermic (∆H°: 12.9 kJ mol -1 ), with positive entropy (∆S°: 125 J mol -1  K -1 ). Uptake kinetics are controlled by agitation speed (optimum ≈200 rpm) and resistance to intraparticle diffusion. The profiles are strongly affected by the mode of agitation: the equilibrium time (≈180 min) is reduced to 20-30 min under sonication (especially at frequency: 80 kHz). The mode of agitation controls the best fitting equation: pseudo-first order rate agitation for mechanical agitation contrary to pseudo-second order rate under sonication. The sorption of MB is poorly affected by ionic strength (loss <6 % in 45 g L -1 NaCl solution). Desorption (faster than sorption) is completely achieved using 0.7 M HCl solution. At the sixth recycling, the loss in sorption is close to 5 % (≈ decrease in desorption efficiency). The process is successfully applied for the treatment of MB-spiked industrial solution: the color index decreases by >97 % with a sorbent dose close to 1 g L -1 ; a higher dose is required for maximum reduction of the COD (60 % at 3 g L -1 )., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

In this research, Orobanche aegyptiaca extract was utilized as an eco-friendly, and cost-effective green route for the construction of bimetallic silver-selenium nanoparticles (Ag-Se NPs). Bimetallic Ag-Se NPs were characterized by XRD, EDX, FTIR, HR-TEM, DLS, SEM/mapping and EDX studies. Antimicrobial, and antibiofilm potentials were tested against some selected pathogenic bacteria and unicellular fungi by ZOI, MIC, effect of UV exposure, and inhibition %. Reaction mechanism was assessed through membrane leakage assay and SEM imaging. HRTEM analysis confirmed the spherical nature and was ranged from 18.1 nm to 72.0 nm, and the avarage particle size is determined to be 30.58 nm. SEM imaging prove that bimetallic Ag-Se NPs presents as a bright particles, and both Ag and Se were distributed equally across O. aegyptiaca extract and Guar gum stabilizers. ZOI results showed that, bimetallic Ag-Se NPs have antimicrobial activity against S. aureus (20.0 nm), E. coli (18.5 nm), P. aeruginosa (12.6 nm), and C. albicans (18.2 nm). In addition, bimetallic Ag-Se NPs were able to inhibit the biofilm formation for S. aureus by 79.48%, for E. coli by 78.79%, for P. aeruginosa by 77.50%, and for C. albicans by 73.73%. Bimetallic Ag-Se NPs are an excellent disinfectant once it had excited by UV light. It was observed that the quantity of cellular protein discharged from S. aureus is directly proportional to the concentration of bimetallic Ag-Se NPs and found to be 244.21 μg/mL after the treatment with 1 mg/mL, which proves the antibacterial characteristics, and explains the creation of holes in the cell membrane of S. aureus producing in the oozing out of the proteins from the S. aureus cytoplasm. Based on the promising properties, they showed superior antimicrobial potential at low concentration (to avoid toxicity) and continued-phase durability, they may use in pharmaceutical and biomedical applications., Competing Interests: Declaration of competing interest The authors declare that they have no conflict of interest., (Copyright © 2023 Elsevier Inc. All rights reserved.)

Climate change is being currently faced globally; controlling the plastic waste and gas emission is aimed to reduce their hazardous effects. In this work, polyethylene terephthalate (PET) and polyvinyl chloride (PVC) polymer wastes are used as fillers to calcium silicate. Chemical treatment was performed to get the best efficiency of the binder material with the treated PET (TPET) and treated PVC (TPVC). The used silicate, new nonhydraulic dicalcium silicate, was synthesized by sintering. A new environmentally friendly polymer concrete, based on different concentrations of PET-/TPET-/PVC-/TPVC-dicalcium silicate composites, was prepared and cured by carbonation. FTIR analysis confirms that the treatment gave functional groups on the polymer surface; also, the hydrophilicity was increased after treatment. SEM photos show that the treated polymers have a rougher surface, which led to improved attachment with cement. The structures of the prepared and cured cement materials are proved by XRD, FTIR analysis, and SEM, through the change of calcium silicate to carbonate. Carbon footprint is used to analyze the environmental implications of the prepared composites. After the treatment reaction, the TPET-cement and TPVC-cement composites showed improved compression and flexural properties and more stability against water absorption. The novelty arises from recycling this plastic waste in the proposed low-energy dicalcium silicate cement, for the first time, to give improved environmentally friendly composites after converting CO 2 gas to carbonates, with the reduced carbon footprint., Competing Interests: The authors declare no competing financial interest., (© 2023 The Authors. Published by American Chemical Society.)

Recently, scientist study the role of surfactants for carbon steel corrosion protection. In the present study, newly tetra-cationic surfactant (CS4: 1,N1'-(ethane-1,2-diyl) bis (N1, N2-didodecyl-N2-(2- (((E)-3-hydroxy-4-methoxy-benzylidene)amino)ethyl)ethane-1,2-diaminium) chloride) based on Schiff-base compound(5,5'-((1E,17E)-2,5,8,11,14,17-hexaazaoctadeca-1,17-diene-1,18-diyl)bis(2-methoxyphenol) was synthesised, purified and characterized using FTIR and 1 HNMR spectroscopy. The synthesized Tetra-cationic surfactant (CS4) was evaluated as anti-corrosion for carbon steel (CS-metal) in aggressive 1 M HCl using electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization techniques (PDP). CS4 compound had a good surface-active property by reducing the surface tension as a result to the hydrophobic chains role. The prepared CS4 behaved as hybrid inhibitor (mixed-type) by blocking the anodic and cathodic sites. CS4 exhibited good inhibition efficiency reached 95.69%. The surface morphology of CS-metal was studied using scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS)confirming the anti-corrosive effect of CS4 compound returned into the adsorption process of CS4 molecules over CS-metal which obeyed Langmuir adsorption isotherm. The inhibitive effect of CS4 was supported by theoretical quantum chemical studies using the density functional theory (DFT), Monte Carlo (MC) and Molecular Dynamic (MD) simulation., (© 2023. The Author(s).)

Two cationic surfactants based on thiazine, dodecyl thiazin bromide (DTB) and hexyl thiazin bromide (HTB), were synthesized, characterized, and investigated as corrosion inhibitors for API X-65 type steel in oil wells' formation water under an H 2 S environment. Various spectroscopic techniques such as FTIR and 1 H NMR were used to confirm the DTB and HTB chemical structures. The corrosion inhibition efficiency of the selected compounds was investigated using both potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) measurements. The innovation of the current study is the existence of a long chain in the inhibitor molecule, which leads to an increase in the performance of the surfactant as a corrosion inhibitor, due to the increase in the surface area per molecule. It was found that these surfactants act as mixed-type inhibitors, leading to suppression of both the cathodic and the anodic processes by its adsorption on the electrode surface according to the Langmuir adsorption isotherm. Carbon steel's inhibitory mechanism was studied using an analogous circuit. The scanning electron microscope technique was used as a suitable analysis tool to show the nature of the layer designed on carbon steel. Quantum chemical calculations and Monte Carlo simulation techniques were used to support the obtained experimental results. Finally, a suitable mechanism for the inhibition process was proposed and discussed., Competing Interests: The authors declare no competing financial interest., (© 2022 The Authors. Published by American Chemical Society.)

Water shortages have become a serious issue, so the importance of developing innovative cellulose-based superabsorbent polymer (SAP) was experimentally assessed as an environmentally friendly alternative to acrylate-based SAPs for the optimization of water consumption. The development of a biodegradable superabsorbent hydrogel composite based on a graft copolymer of carboxymethyl cellulose (CMC) and mixtures of different comonomers such as an acrylamide- co -acrylic acid- co -2-acrylamido-2-methylpropanesulfonic acid (Am- co -AA- co -AMPS) CMC- g -TerPoly interpenetrating network was characterized by infrared spectroscopy (FT-IR), scan electron microscopy (SEM), atomic force microscope (AFM), thermal gravimetric analysis (TGA), and swelling capacity in different aqueous media. The optimized CMC- g -(TerPoly) composite showing outstanding superabsorbance with high water retention, the ratio of constituents, temperature, and pH effect on equilibrium swelling have been optimized by using multistage response surface methodology (RSM). In distilled water (d-water), the equilibrium water absorption capacity (EW) of the synthesized composite hydrogels (SAP-IPN1) is 1200 g (d-water/1g hydrogel) which is superior to any other commercial polyacrylate SAP hydrogels, while in saline water the EW is 650 g (s-water/1g hydrogel). The performance of the SAP-IPN for water retention was evaluated by studying several swelling/deswelling cycle measurements. The prepared SAP-IPN hydrogels were found to show pH and salt solution dependence on the swelling behavior. The new SAP-IPN can work with commercial SAP, which is recommended for application as a water reservoir in arid land for irrigation for agriculture purposes., Competing Interests: The authors declare no competing financial interest., (© 2022 The Authors. Published by American Chemical Society.)

Uranium is the backbone of the nuclear fuel used for energy production but is still a hazardous environmental contaminant; thus, its removal and recovery are important for energy security and environmental protection. So far, the development of biocompatible, efficient, economical, and reusable adsorbents for uranium is still a challenge. In this work, a new orange peel biochar-based hydrogel composite was prepared by graft polymerization using guar gum and acrylamide. The composite's structural, morphological, and thermal characteristics were investigated via Fourier transform infrared (FTIR), scanning electron microscope (SEM), X-ray diffraction (XRD), and thermogravimetric analysis (TGA) methods. The composite's water absorption properties were investigated in different media. The performance of the prepared composite in adsorbing uranium (VI) ions from aqueous media was systematically investigated under varying conditions including solution's acidity and temperature, composite dose, contact time, and starting amount of uranium. The adsorption efficiency increased with solution pH from 2 to 5.5 and composite dose from 15 to 50 mg. The adsorption kinetics, isotherms, and thermodynamics parameters were analyzed to get insights into the process's feasibility and viability. The equilibrium data were better described through a pseudo-second-order mechanism and a Langmuir isotherm model, indicating a homogeneous composite surface with the maximum uranium (VI) adsorption capacity of 263.2 mg/g. The calculated thermodynamic parameters suggested that a spontaneous and endothermic process prevailed. Interference studies showed high selectivity toward uranium (VI) against other competing cations. Desorption and recyclability studies indicated the good recycling performance of the prepared composite. The adsorption mechanism was discussed in view of the kinetics and thermodynamics data. Based on the results, the prepared hydrogel composite can be applied as a promising, cost-effective, eco-friendly, and efficient material for uranium (VI) decontamination., Competing Interests: The authors declare no competing financial interest., (© 2021 The Authors. Published by American Chemical Society.)

Irradiated waste high-density polyethylene@Zn/ionic liquid novel composite well-fabricated via coacervation method was irradiated by gamma-irradiation and studied the effect of that radiation on the desulfurization process. The prepared composites were characterized by various analytical techniques as follows: X-ray diffraction (XRD), Fourier-Transform infrared (FT-IR), X-ray photoelectron spectrometer (XPS), scanning electron microscope (SEM), High Resolution Transmission Electron Microscopy (HRTEM), N 2 -adsorption-desorption isotherm, and thermal gravimetric analysis (TG/DTA). The adsorptive desulfurization process of benzothiophene (BT) and dibenzothiophene (DBT) which are harmful compounds in diesel model fuel was investigating using the irradiated and unirradiated composite. The results illustrated that the unirradiated and irradiated composites exhibit an adequate adsorption capacity reached (50-75 mg S/g) and (60-85 mg S/g) for BT and DBT, respectively. The adsorption process over the prepared adsorbents follows the pseudo-second-order kinetic models. The irradiated composite exhibited more adsorption capacity than the unirradiated one due to the radiation generated more surface area and created proton-bond donor sites in the composite surface, which increases the interaction between the surface and sulfur species. The adsorption capacity and adsorption percentage for irradiated and unirradiated composites towards (SCCs) were studied using response surface methodology based on the central composite design (CCD). The thermodynamic factors (∆H°, ∆G°, and ∆S°) reveal that these processes are endothermic adsorption processes. The irradiated PEt @Zn/IL was re-used without significant loss of adsorption activity. This novel irradiated PEt @Zn/IL is the first time used as an adsorbent with an advantage that includes its excellent adsorption capacity, which ensures the product will be efficient in a real process such as the petrochemical industry., (© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Improving oil production for high-salinity reservoirs using polymer flooding is challenging due to chemical and mechanical degradations. This study developed two biodegradable biopolymers based on graft copolymerization of guar gum (GG) with two different co-monomers, which are acrylamide (Am) and 2-acrylamido-2-methylpropane sulfonic acid (AMPS), and cross-linked by N,N '-methylene bisacrylamide (MBA) to face these challenges. The newly synthesized guar gum-based hydrogels, GG- g -poly(Am-AMPS) (GH) and GG- g -poly(Am-AMPS)/Biochar (GBH composite), were evaluated as potential candidates for enhanced oil recovery (EOR) under high-salinity conditions. Fourier transform infrared (FTIR) spectroscopy and thermogravimetric analysis (TGA) of the synthesized hydrogels were investigated, and their rheological properties were measured at room temperature. Both GH and GHB display a shear-thinning performance. In polymer flooding experiments, guar gum hydrogel (GH) and guar gum/biochar composite hydrogel (GHB) showed a remarkable influence on delaying the water breakthrough and proved to be effective biopolymers for enhanced oil recovery in high-salinity reservoirs. At the optimum concentration of 5 g/L, GH flooding achieved maximum oil recoveries of 70.53 and 72.11% in secondary and tertiary recovery processes, respectively. Meanwhile, the waterflooding process achieved an ultimate oil recovery of 58.42%. GHB flooding at optimum concentration, 2 g/L, increased the amount of oil recovery by 8.95% in tertiary recovery compared to waterflooding. Furthermore, GH (5 g/L) and GHB (2 g/L) slightly enhanced the rock water wettability as confirmed by contact angle measurements for GH and the relative permeability saturation curves for GH and GHB., Competing Interests: The authors declare no competing financial interest., (© 2021 The Authors. Published by American Chemical Society.)

The inhibition efficiency of cationic surfactants such as 1-ethyl-4 H -benzo[d][1,3]thiazin-1-ium bromide (BTB) and N -ethyl- N,N -dioctyloctan-1-aminium bromide (DAB) for X-65 type carbon steel in oil well formation water under a H 2 S environment has been studied using potentiodynamic polarization and electrochemical impedance spectroscopy measurements. Fourier transform infrared and nuclear magnetic resonance spectroscopy techniques were used to confirm the chemical structures of BTB and DAB. The novelty of this work lies in modifying the long chains in the inhibitor, which leads to high efficiency. These surfactants act as good inhibitors, which inhibit both cathodic and anodic routes by adsorption on the electrode surface, which is compatible with the critical micelle concentration parameters, together with a slight positive change in the corrosion potential ( E corr ). The IE% reached 93.4% for compound BTB and 84% for compound DAB at 250 ppm. The equivalent circuit was used to analyze the model of the corrosion inhibition process. The atomic force microscopy image shows the morphology of the adsorbed layer formed on the steel alloy. Finally, a suitable inhibition mechanism was proposed., Competing Interests: The authors declare no competing financial interest., (© 2021 The Authors. Published by American Chemical Society.)

The inhibitory impact of low-cost synthesized pyrazoline derivatives named Pz series ( Pz1 and Pz2 ) on the corrosion of API 5L X60 carbon steel in 5 M HCl was inspected to serve as corrosion inhibitors against such a solution for its usage in the oilfield well acidization process. Also, the same compounds were unitized as biocides for sulfate-reducing bacteria (SRBs) to inhibit the microbial-induced corrosion effect. This study was conducted via several electrochemical techniques, namely, electrochemical potentiodynamic polarization (EP) and electrochemical impedance spectroscopy (EIS), in addition to computational density functional theory (DFT). The inhibition efficiency (IE) of Pz series on the corrosion of 5L X60 carbon steel in 5 M HCl was found to increase whenever the Pz series molecule concentration was increased. EP measurements revealed that Pz1 and Pz2 have both cathodic and anodic features (mixed inhibitor) and their corrosion IEs were around 90%. The physicochemical properties of the Pz1 and Pz2 compounds were studied using Langmuir adsorption isotherms, where the equilibrium adsorption data were found to follow it accurately. EIS outputs were found to comply with the values obtained from EP. Scanning electron microscopy was used to examine the topographic anisotropy between the inhibited and uninhibited 5L X60 carbon steel samples to double-check the electrochemical findings. DFT calculations and Monte Carlo simulations were utilized to predict the behavior of inhibitors and to rationalize the experimental results. The serial dilution bioassay technique was used to assess the Pz series as potential biocides to counter the effect of SRBs in compliance with the TM0194-2014-SG standard test method, and the results showed the potency of Pz series in inhibiting such bacterial growth., Competing Interests: The authors declare no competing financial interest., (© 2021 The Authors. Published by American Chemical Society.)

Ionic liquids have significantly enhanced ecofriendly benefits compared to the traditional inhibitors. In the present work, new four polymeric ionic liquids based on benzoimidazole derivatives were synthesized through the reaction of 2-styryl-1 H -benzo[ d ]imidazole with alkyl halide to form PIL1. Then, Cl - anions were exchanged with different anions through the neutralization reaction to form other investigated polymers. Their structures were chemically elucidated using Fourier transform infrared spectroscopy, 1 H NMR, and 13 C NMR. Their influence on carbon steel (CS) as corrosion inhibitors has been checked with dielectric spectroscopy in addition to potentiodynamic polarization curves. It was found that the percentage of inhibition efficiency increases as inhibitor's concentrations increase, suggesting a decrease in the rate of CS corrosion. Additionally, the hydrogen evolution rate controlled by the four polymers was monitored. Addition of the prepared polymers lessened the rate of generation of hydrogen as the inhibitor's concentrations augmented. Scanning electric electron microscopy in addition to energy-dispersive X-ray diffraction has proved the morphology of the CS surface as well as the formed protective film., Competing Interests: The authors declare no competing financial interest., (© 2020 American Chemical Society.)

The target of this study is the synthesis of a new diester derivative and radiolabeling with one of the most effective diagnostic radioisotopes to be investigated as a novel targeting radiotracer for tumor imaging. 10-[2-(9-Carboxynonanoyloxy)propoxy]-10-oxodecanoic acid was synthesized in excellent yield and characterized by Fourier-transform infrared spectroscopy, mass, 1 H-NMR, and 13 C-NMR spectra. The diester was technetium-99m ( 99m Tc) radiolabeled by direct technique using sodium dithionite as a reducing agent. The labeling parameters such as diester amount, reducing agent amount, pH of the medium, and reaction time were optimized. High radiochemical yield of 95.10 ± 0.41% and in vitro stability in serum up to 12 h have been obtained on complexation of the synthesized diester with Tc-99m. Evaluation of the diester anticancer activity against breast cancer cell line (MCF-7) showed high percent of inhibition about 61.5% at 100 μg/ml. The rhenium complex of the diester was synthesized and characterized by liquid chromatography-mass spectrometry (ESI) and elemental analysis depending on the strong chemical resemblance between Tc and Re. Biodistribution studies of 99m Tc-diester complex showed high target to nontarget ratio (T/NT) equals 6.24 ± 0.09 in tumor-bearing mice at 30-min postinjection, suggesting this complex could be used as hopeful solid tumor-imaging agent., (© 2020 John Wiley & Sons, Ltd.)

A novel adsorbent based on N-Aminorhodanine modified chitosan hydrogel was synthesized and evaluated for antibacterial and copper ions removal from aqueous systems. N-Aminorhodanine was reacted with glutaraldehyde to yield Schiff base followed by reaction with chitosan to obtain the new hydrogel adsorbent. The new adsorbent was analyzed using FTIR, 1 H NMR, XRD, TGA, HR-SEM and EDX in addition to the swelling behavior. The maximum adsorption capacities of chitosan and modified chitosan for copper ions were 38 and 62.5 mg/g respectively. The adsorption isotherm belongs Freundlich model and pseudo second order kinetics regime. The adsorption was reach to maximum within 15 min for modified chitosan hydrogel while take about 360 min for chitosan. Regeneration of adsorbent showed only 23% decline after 6 cycles which indicate the stability of the new adsorbent and it can be reused several times with good efficiency. N-Aminorhodanine modified chitosan hydrogel showed good activity towards gram positive bacteria., Competing Interests: Declaration of competing interest The authors declare that they have no conflict of interest., (Copyright © 2018. Published by Elsevier B.V.)

In this work, we report the synthesis of two Schiff bases of substituted gallic acid derivatives via amidation reaction and their characterization using 1 H-NMR spectroscopy to study their inhibition performance on the aggressive attack of HCl on mild steel (MS). The inhibitive performance was examined using chemical (weight loss) and electrochemical (Tafel and EIS) test methods. The results indicate that these derivatives significantly suppress the dissolution rate of mild steel via adsorption phenomena, which correlates to the Langmuir adsorption model. Tafel data display the mixed-type properties of these compounds and EIS results show that increasing Schiff base concentration not only leads to delaying the charge transfer ( R ct ) of iron from 26.4 ohm cm -2 to 227.7 ohm cm -2 but also decreases the capacitance of the adsorbed double layer ( C dl ) from 8.58 (F cm -2 ) × 10 -5 to 2.55 (F cm -2 ) × 10 -5 . The inhibition efficiency percentage reaches the peak (90%) at optimum concentration of 250 ppm. The Monte Carlo simulations confirm the adsorption ability of the as-prepared compounds on the Fe (1 1 0) crystal. The SEM/EDX results revealed the presence of a protective film on the mild steel sample., Competing Interests: There are no conflicts of interest to declare, (This journal is © The Royal Society of Chemistry.)

The corrosion performance of carbon steel was tested in four polymeric ionic liquids (PILs) that differed only in the fatty acid linked to the chitosan (CS) amine group. The measurements were implemented involved the hydrogen evolution rate (HER), gravimetric measurements, potentiodynamic polarization (PDP), electrochemical impedance spectroscopy (EIS), and quantum chemical estimations. The morphology and the elements arranged on the metal were considered by a scanning electron microscopy (SEM) system attached to an energy dispersive X-ray (EDX) system. The addition of polymeric ionic liquids hindered the rate of hydrogen generation. The order of the inhibitors efficiency was CSPTA-lauric > CSPTA-myristic > CSPTA-palmitic > CSPTA-stearic. The polarization method proved that the percentage inhibition efficiency increases with increasing the inhibitors concentration in 1 M HCl, representing a drop in the corrosion rate of carbon steel. On the other hand, the percentage inhibition decreased with the increase in temperature. Quantum chemical calculations revealed that the tested ionic liquids could react with the iron surface via electron transfer from the metal atom to ionic liquid molecule., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)