NANO-CHARACTERIZATION OF TYPE-G CEMENT SLURRY INCORPORATING NANOCLAY CURED UNDER HIGH TEMPERATURE AND PRESSURE

Abstract: Type-G cement slurry with various admixtures commonly used in oil/gas well cementing (OWC) incorporating 1, 2 and 3% nanoclay particles by weight of cement were produced. A water/cement ratio of 0.44 was used and the mixes were subjected to a temperature of 290° F and a pressure of 4666 psi for 48 hours. First, the effect of nanoclay on compressive strength evolution was investigated. Second elastic and viscoelastic characteristics of the cementitious mixes were characterized using nanoindentation. The nanoindentation tests enabled evaluating the maximum indentation depth, plastic depth, and the reduced elastic modulus. Furthermore, dwell time of 60 seconds was used to evaluate creep compliance of the cement mixes incorporating nanoclay. Fracture toughness was estimated from the nanoindentation data during the dwell loading period. Scanning electron microscope (SEM) and X-ray diffraction (XRD) microstructural analyses were conducted to explain the results observed using nanoindentation. Furthermore, finite element modeling was used to simulate the nanoindentation test and to extract the stress-strain Type-G cement material incorporating nanoclay and cured under high temperature and pressure. Moreover, The experimental observations showed that nanoclay improved compressive strength evolution with time compared with neat cement and eliminated strength retrogression problem. Furthermore, using 1 and 2% nanoclay resulted in insignificant change (-28 to +12%) of the reduced elastic modulus compared with neat cement. However, a high content of 3% nanoclay resulted in a significant increase of (+54%) in the reduced elastic modulus and a significant reduction in creep compliance compared with neat cement. Fracture analysis of nanoindentation data showed a significant improvement of fracture toughness due to the addition of nanoclay. XRD analysis and SEM investigations proved that the incorporation of nanoclay in the cement mix transforms the Calcium Hydroxide (CH) to calcium silicate hydrate (C-S-H) and reduced capillary porosity leading to higher elastic modulus and reduced creep compliance compared with neat cement. Finally, the extracted stress-strain curves using the finite element method shows that adding nanoclay resulted in stiffening OWC paste. The significance of nanoclay seems strongly dependent on the nanoclay content and the quality of its mixing with cement

Data on the fabrication of hybrid calix [4]arene-modified natural bentonite clay for efficient selective removal of toxic metals from wastewater at room temperature

Fresh water resources on the earth are less than 0.2%; meanwhile, around 80% of the freshwater is consumed daily in agriculture, industries, and household activities [1–2]. There is an essential need to develop efficient adsorbents for wastewater treatment [1–6], in this regards, hereafter we present the rationale synthesis and characterization of hybrid natural bentonite clay modified with Calix [4] arene (denoted as B-S-Calix) as efficient adsorbents for toxic metals from wastewater. This is driven by the facile photo-radical thiol-yne addition among the thiolated clay and an alkynylated calix[4]arene. The morphology, surface modifications, and Thermal degradation of B, B-S, and B-S-Calix were investigated using TEM, FTIR, and TGA techniques. The adsorption performance of B, BS and B-S-Calix towards toxic metals including cadmium (II) ion [Cd (II)], zinc (II) ion [Zn(II)], lead(II) ion [Pb(II)], strontium(II) ion [Sr (II)], cobalt(II) ion [Co (II)], copper(II) ion [Cu(II)], and mercury (II) ion [Hg(II)] from wastewater were benchmarked 25 °C. These data are related to the article entitled “hybrid Clay/Calix[4]arene Calix[4]arene-clicked clay through thiol-yne addition for the molecular recognition and removal of Cd(II) from wastewater’’ [7]

Spectral, thermal, antimicrobial studies for silver(I) complexes of pyrazolone derivatives

Background: Synthesize new complexes of Ag(I) to enhance efficacy or stability and also, pharmacological activities on the operation of pyrazolone's biological properties. Results: Efficient and high yielding pathways starting from the versatile and readily available 3-methyl-1-phenyl-5-pyrazolone by Knoevenagel condensation of a sequence of 4-arylidene-3-methyl-1-phenyl-5-pyrazolone derivatives (2a-c) have been formed by the reaction of various substituted aromatic aldehydes Used as ligands to synthesize Ag(I) chelates. Synthesized compounds and their complexes have been characterized by elemental analysis, magnetic and spectroscopic methods (IR, 13C, 1HNMR, mass) and thermal analysis. The spectrophotometric determinations suggest distorted octaedral geometry for all complexes. Both ligands and their metal complexes have also been tested for their antibacterial and antifungal efficacy. Conclusions: Newly synthesized compounds have shown potent antimicrobial activity. The results showed that the complex 's high activity was higher than its free ligands, and that Ag(I)-L3 had the highest activity.This research is not funded though any source to This publication was supported by Qatar University, internal grant number QUCG-CAM-20/21-2. The findings achieved herein are solely the responsibility of the authors

Caprylamidopropyl Betaine as a Highly Efficient eco-friendly Corrosion Inhibitor for API X120 Steel in 1 M H2SO4

CORROSION inhibition of API X120 steel in a 1M sulfuric acid solution at altered temperatures was investigated utilizing a new eco-friendly surfactant (Caprylamidopropyl Betaine (CAPB)) by Gravimetric and electrochemical test (containing potentiodynamic polarization (PP), electrochemical impedance spectroscopy (EIS). Surface characterization tests containing scanning electron microscopy (SEM), and atomic force microscopy (AFM) are utilized in the study. In addition, kinetic and thermodynamic parameters were measured and discussed. The overall results displayed that the corrosion rate of API X120 steel was significantly lowered with improving the temperature. The polarization curves lead to the CAPB inhibitor is influenced both anodic and cathodic reactions (mixed type inhibitor). Analyses of the surface topography designated an appreciable decrease in the surface roughness as the dose of the inhibitor in the solution improved. Energy-dispersive X-ray and X-ray photoelectron spectroscopy revealed the presence of adsorbed nitrogen atoms on the API X 120 steel surfaces. This work provides a promising eco-friendly inhibitor for mitigating the corrosion of API X120 steel in highly acidic brine environments

Rational synthesis, characterization, and application of environmentally friendly (polymer–carbon dot) hybrid composite film for fast and efficient UV-assisted Cd²⁺ removal from water

Background: Carbon dots (CDs) are of particular interest in numerous applications. However, their efficiency for heavy metal removal from wastewater was not yet reported. Herein, we rationally synthesized CDs from petroleum coke waste via hydrothermal treatment in the presence of ammonia. Results: This drove the formation of outstanding photoluminescent, water-soluble, biocompatible, and high yield of monodispersed sub-5 nm CDs. The CDs are co-doped with high 10% of N and 0.2% of S. The as-prepared CDs possess unprecedented photoluminescent properties over broad pH range making these dots unique efficient pH sensor. Conclusions: Chitosan (CH)–CDs hybrid hydrogel nanocomposite film was further prepared as a platform membrane for the removal Cd2+ metal from wastewater. The as-prepared CH–CDs membranes show relatively good mechanical properties, based on stress resistance and flexibility to facilitate handling. The equilibrium state was reached within 5 min. Intriguingly, the UV-light illuminations enhanced the Cd2+ removal efficiency of the photoluminescent CDs substantially by four times faster under. It was found that adsorption followed pseudo-second-order kinetic and Langmuir isotherm models. The maximum adsorption capacity at 25 °C was found to be 112.4 mg g−1 at pH 8. This work paves the way to new applications of CDs in water treatment.[Figure not available: see fulltext.]

An efficient green ionic liquid for the corrosion inhibition of reinforcement steel in neutral and alkaline highly saline simulated concrete pore solutions

The effect of the green ionic liquid compound, Quaternium-32 (Q-32), on the corrosion inhibition performance of reinforcement steel, in a simulated concrete pore solution, was investigated at different temperatures and pH values, using electrochemical impedance spectroscopy (EIS). The inhibition efficiency was improved as the concentration of Q-32 and pH values were increased. However, it decreased as the temperature was raised. A Q-32 concentration of 20 µmol L–1 exhibited a 94% inhibition efficiency at 20 °C. The adsorption isotherm was evaluated using EIS measurements, and it was found to obey the Langmuir isotherm. The surface topography was examined using an atomic force microscope and scanning electron microscope. The effect of the Q-32 concentration with the highest corrosion efficiency on the mechanical properties of the mortars was also explained by flexure and compression techniques.The authors express their gratitude to the Center for Advanced Materials at Qatar University for technical support. Additionally, the authors are grateful to Qatar University for funding this work through the QUCG-CAM-20/21-2 Grant. The publication of this article was funded by the Qatar National Library

Organ-specific toxicity evaluation of stearamidopropyl dimethylamine (SAPDMA) surfactant using zebrafish embryos

Surfactants are widely used in the industry of detergents, household products, and cosmetics. SAPDMA is a cationic surfactant that is used mostly in cosmetics, conditioning agents and has recently gained attention as a corrosion inhibitor in the sea pipelines industry. In this regard, literature concerning the ecotoxicological classification of SAPDMA on aquatic animals is lacking. This study aims to evaluate the potential ecotoxicity of SAPDMA using the aquatic zebrafish embryo model. The potential toxic effects of SAPDMA were assessed by different assays. This includes (i) mortality/survival assay to assess the median lethal concentration (LC50); (ii) teratogenicity assay to assess the no observed effect concentration (NOEC); (iii) organ-specific toxicity assays including cardiotoxicity, neurotoxicity (using locomotion assay), hematopoietic toxicity (hemoglobin synthesis using o-dianisidine staining), hepatotoxicity (liver steatosis and yolk retention using Oil Red O (ORO) stain); (iv) cellular cytotoxicity (mitochondrial membrane potential) by measuring the accumulation of JC-1 dye into mitochondria. Exposure of embryos to SAPDMA caused mortality in a dose-dependent manner with a calculated LC50 of 2.3 mg/L. Thus, based on the LC50 value and according to the Fish and Wildlife Service (FWS) Acute Toxicity Rating Scale, SAPDMA is classified as “moderately toxic”. The No Observed Effect Concentration (NOEC) concerning a set of parameters including scoliosis, changes in body length, yolk, and eye sizes was 0.1 mg/L. At the same NOEC concentration (0.1 mg/L), no organ-specific toxicity was detected in fish treated with SAPDMA, except hepatomegaly with no associated liver dysfunctions. However, higher SAPDMA concentrations (0.8 mg/L) have dramatic effects on zebrafish organ development (eye, heart, and liver development). Our data recommend a re-evaluation of the SAPDMA employment in the industry setting and its strictly monitoring by environmental and public health agencies

Enhanced mechanical and corrosion protection properties of pulse electrodeposited NiP-ZrO2 nanocomposite coatings

Pulse electrodeposition is a technique of particular interest, which offers promising advantages such as ease of processing, compositional control, uniformity in structure, and grain refinement. In the present study, NiP-ZrO2 nanocomposite coatings containing various concentrations of ZrO2 nanoparticles (ZONPs) were deposited on low alloy steel (30CrMnSi) through pulse electrodeposition technique. The ZONPs in concentration of 0.0, 0.25, 0.50, 0.75, and 1.0 g/L were added in the electrolyte bath to obtain NiP-ZrO2 nanocomposite coatings. Furthermore, to elucidate the role of ZONPs in the NiP matrix, the structural, morphological, mechanical, and electrochemical properties of NiP-ZrO2 nanocomposite coatings were studied thoroughly. FESEM and EDX results reveal the successful incorporation of ZONPs into the NiP matrix. XRD and XPS analysis confirm the formation of a pure phase NiP structure without any noticeable defects. A considerable improvement in the mechanical response was observed with an increasing amount of ZONPs, reaching to highest values (hardness 6.7 GPa, modulus of elasticity 21.72 GPa) for NiP-1.0 ZrO2 coating composition. Similarly, the electrochemical results show a gradual increase in corrosion protection behavior of the NiP-ZrO2 coatings with increasing ZONP concentration, reaching an eventual value ~5.8 kΩ cm−2 at NiP-1.0 ZrO2 coating composition, which is six times greater than the pure NiP coatings. These improvements in the mechanical and electrochemical response of NiP-ZrO2 nanocomposite coatings highlight their suitability for applications such as oil and gas pipelines

Eco-Friendly Synthesis, Biological Evaluation, and In Silico Molecular Docking Approach of Some New Quinoline Derivatives as Potential Antioxidant and Antibacterial Agents

A new series of quinoline derivatives 5–12 were efficiently synthesized via one-pot multicomponent reaction (MCR) of resorcinol, aromatic aldehydes, β-ketoesters, and aliphatic/aromatic amines under solvent-free conditions. All products were obtained in excellent yields, pure at low-cost processing, and short time. The structures of all compounds were characterized by means of spectral and elemental analyses. In addition, all the synthesized compounds 5–12 were in vitro screened for their antioxidant and antibacterial activity. Moreover, in silico molecular docking studies of the new quinoline derivatives with the target enzymes, human NAD (P)H dehydrogenase (quinone 1) and DNA gyrase, were achieved to endorse their binding affinities and to understand ligand–enzyme possible intermolecular interactions. Compound 9 displayed promising antioxidant and antibacterial activity, as well as it was found to have the highest negative binding energy of -9.1 and -9.3 kcal/mol for human NAD (P)H dehydrogenase (quinone 1) and DNA gyrase, respectively. Further, it complied with the Lipinski’s rule of five, Veber, and Ghose. Therefore, the quinoline analogue 9 could be promising chemical scaffold for the development of future drug candidates as antioxidant and antibacterial agents

Electrochemical and thermodynamic study on the corrosion performance of API X120 steel in 3.5% NaCl solution

The present work studied the effect of temperature on the corrosion behavior of API X120 steel in a saline solution saturated with CO2 in absence and presence of polyethyleneimine (PEI) as an environmentally safe green inhibitor. The effect of PEI on the corrosion behavior of API X120 steel was investigated using destructive and non-destructive electrochemical techniques. The overall results revealed that PEI significantly decreases the corrosion rate of API X120 steel with inhibition efficiency of 94% at a concentration of 100 μmol L−1. The adsorption isotherm, activation energy and the thermodynamic parameters were deduced from the electrochemical results. It is revealed that the adsorption of PEI on API X120 steel surface follows Langmuir adsorption isotherm adopting a Physi-chemisorption mechanism. Finally, the samples were characterized using scanning electron microscopy (SEM) and atomic force microscopy (AFM) techniques to elucidate the effect of aggressiveness of corrosive media on the surface morphology and the corrosion performance of API X120 steel. The surface topography result indicates that the API X120 steel interface in PEI presence is smoother than CO2 with Cl− ions or Cl− ions only. This is attributed to the compact protective film limits the aggressive ions transfer towards the metallic surface and reduces the corrosion rate. Moreover, PEI inhibition mechanism is based on its CO2 capturing ability and the PEI adsorption on the steel surface beside the siderite layer which give the PEI molecules the ability to reduce the scale formation and increase the corrosion protection due to capturing the CO2 from the brine solution