Search

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.)

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.)

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.)

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.)