ABSTRACT
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 CO2 uptake% in the proposed composites reached 16.6%, referring to the successful storage of CO2 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 CO2 gas, and reduce gas emission makes the proposed polymer waste mix-cement composites as environmentally friendly construction products.
ABSTRACT
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 1H NMR and 13C 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.
ABSTRACT
Newly synthesized mono- and bis-thioureidophosphonate (MTP and BTP) analogues in eco-friendly conditions were employed as reducing/capping cores for 100, 500, and 1000 mg L-1 of silver nitrate. The physicochemical properties of silver nanocomposites (MTP(BTP)/Ag NCs) were fully elucidated using spectroscopic and microscopic tools. The antibacterial activity of the nanocomposites was screened against six multidrug-resistant pathogenic strains, comparable to ampicillin and ciprofloxacin commercial drugs. The antibacterial performance of BTP was more substantial than MTP, notably with the best minimum inhibitory concentration (MIC) of 0.0781 mg/mL towards Bacillus subtilis, Salmonella typhi, and Pseudomonas aeruginosa. Among all, BTP provided the clearest zone of inhibition (ZOI) of 35 ± 1.00 mm against Salmonella typhi. After the dispersion of silver nanoparticles (AgNPs), MTP/Ag NCs offered dose-dependently distinct advantages over the same nanoparticle with BTP; a more noteworthy decline by 4098 × MIC to 0.1525 × 10-3 mg/mL was recorded for MTP/Ag-1000 against Pseudomonas aeruginosa over BTP/Ag-1000. Towards methicillin-resistant Staphylococcus aureus (MRSA), the as-prepared MTP(BTP)/Ag-1000 displayed superior bactericidal ability in 8 h. Because of the anionic surface of MTP(BTP)/Ag-1000, they could effectively resist MRSA (ATCC-43300) attachment, achieving higher antifouling rates of 42.2 and 34.4% at most optimum dose (5 mg/mL), respectively. The tunable surface work function between MTP and AgNPs promoted the antibiofilm activity of MTP/Ag-1000 by 1.7 fold over BTP/Ag-1000. Lastly, the molecular docking studies affirmed the eminent binding affinity of BTP over MTP-besides the improved binding energy of MTP/Ag NC by 37.8%-towards B. subtilis-2FQT protein. Overall, this study indicates the immense potential of TP/Ag NCs as promising nanoscale antibacterial candidates.
ABSTRACT
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 CO2 gas to carbonates, with the reduced carbon footprint.
ABSTRACT
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.
ABSTRACT
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.
ABSTRACT
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-1H-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, 1H NMR, and 13C 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.
