Optimization of Water Based Drilling Fluid Properties with the SiO2/g-C3N4 Hybrid.

Drilling fluids are an essential component of drilling operations in the oil and gas industry. Nanotechnology is being used to develop advanced drilling fluid additives. This study looked at the viability of synthesizing SiO2/g-C3N4 hybrid extending the Stober process followed by its addition in different concentrations to water-based drilling fluids and studying impact on the rheological and fluid loss properties of the fluids. The synthesized hybrid was analyzed using XRD, SEM, TGA, and FTIR. Subsequently, it was used to develop the water-based drilling mud formulations and subjected to measurements in accordance with API standard practices. The studies were carried out at various SiO2/g-C3N4 nanoparticle concentrations under before hot rolling (BHR) and after hot rolling (AHR) conditions. The outcomes demonstrated that the rheological and fluid loss properties were enhanced by the addition of SiO2/g-C3N4 nanoparticles, as it worked in synergy with other additives. Additionally, it was discovered that the nanoparticles improved the drilling fluid thermal stability. The experimental findings indicate a significant influence of SiO2/g-C3N4 nanoparticles on base fluid properties including rheology and fluid loss as the most remarkable, especially at higher temperatures. The significant improvements in yield point and 10 s gel strength were 55 and 42.8% under BHR and 216 and 140% under AHR conditions, respectively. Permeability plugging test (PPT) fluid loss was reduced by 69.6 and 87.2% under BHR and AHR conditions, respectively, when 0.5 lb/bbl nanoparticles were used in formulations. As a result, SiO2/g-C3N4 nanomaterial has the potential to be used as drilling fluid additive in water-based drilling fluids.

Fabrication of MoS2/rGO hybrids as electrocatalyst for water splitting applications.

Environmental degradation and energy constraint are important risks to long-term sustainability in the modern world. Water splitting is a vital approach for environmentally friendly and sustainable energy storage, providing a clean way to produce hydrogen without pollutants. Preparing a catalyst that is active, bifunctional, and durable for water splitting is a difficult task. We addressed the difficulty by creating a bifunctional heterogeneous catalyst, MoS2/rGO, with an ideal weight percentage of 5 wt% by a hydrothermal process. The optimized sample showed exceptional electrocatalytic activity, requiring an overpotential of 242 mV and 120 mV to achieve a current density of 10 mA cm-2 in the Hydrogen Evolution Reaction (HER) and Oxygen Evolution Reaction (OER). Furthermore, our synthesized catalyst was validated for its exceptional water-splitting capacity, with the optimized sample showing low Tafel slope values of 59 mV dec-1 for HER and 171 mV dec-1 for OER. The significant OER and HER activity seen in the 5 wt% MoS2/rGO hybrid, compared to other hybrids, is due to the many catalytic active sites that aid in charge and electron transport, as well as the synergistic interaction between MoS2 and rGO.

Free-Flowing Polymer-Bonded Powder Composition of Hexahydro-1,3,5-trinitro-1,3,5-triazine Using Solvent-Slurry Coating.

A number of coating techniques have been used to improve the processability of high explosives. These techniques are typically used for developing compositions, such as boosters and fillers. The most typically used technique is the "solvent-slurry coating". Several compositions of polymer-bonded explosives have been industrialized using this technique. The NUPC-6 polymer-bonded powder composition of hexahydro-1,3,5-trinitro-1,3,5-triazine is optimized using the solvent-slurry coating. It involved multiple processes, i.e., preparing a slurry of high explosives in an aqueous phase, dissolving the modified polymer binder in an organic solvent, maintaining both the solvent and slurry at controlled temperatures, introducing polymer binder solution and ingredients in the slurry, distilling the solvent, mixing contents homogeneously, filtering the polymer-coated hexahydro-1,3,5-trinitro-1,3,5-triazine composition, and drying in a vacuum oven. The phlegmatizing and hydrophobic agents enhance flowability and hydrophobicity. The mass flow rate, bulk density, tapped density, compressibility index, and Hausner ratio are determined to evaluate its flowability during filling operations. The results show that the composition is flowable using a filling funnel, with a 150 mm upper diameter, 25 mm flow diameter, and 136 mm total funnel height. The raw polymer binder was modified using diisooctylsebacate and SAE-10 oil. The additives in the composition enhance its flowability, and it might be used in underwater applications.

Highly porous interconnected MoP decorated graphene oxide as remarkably efficient electrocatalyst.

Hydrogen (H2) production through water splitting has less viable applications due to the unfavourable kinetics of the reaction. Electrocatalysts with a robust structure, high levels of catalytic activity, and a high degree of stability are in high demand but challenging. This paper reports the synthesis of highly porous interconnected molybdenum phosphide (MoP) assembled with graphene oxide (GO) to form MoP/RGO hybrid electrocatalysts in a novel phosphorization process at a reasonably low temperature under an argon (Ar) atmosphere by a mixing and heat-treating method for the hydrogen evolution reaction (HER). Bifunctional MoP anchored on reduced graphene oxide (MoP/RGO) porous structures exhibited extra permeability for ion and electrolyte transport. An efficient MoP/RGO-based electrocatalyst exhibited brilliant electrocatalytic performance, having HER overpotential of 96 mV at a current density of 10 mA/cm2 with a low Tafel slope of 64 mV/dec in an alkaline solution. The effectiveness of an optimised electrocatalyst indicates significant HER activity for all intermediate chemical reactions. A highly efficient electrocatalyst also exhibited long-term stability with a minor potential decrease over 24 h. RGO shows great potential as a material possessing remarkable strength in the context of high temperature phosphorization. It effectively hinders particle agglomeration, enhances catalyst conductivity, and ultimately betters both the performance and durability of an electrocatalyst in HER applications.

Enhanced removal of toxic Cr(vi) and Pb(ii) from water using carboxylic terminated Ti3C2Tx nanosheets.

The discharge of Cr(vi)and Pb(ii) contaminants into water resources through industrial waste induces a considerable risk to human and marine life, which demands an effective removal of these toxic metal ions (MI) from the aquatic environment. This study presents a remarkable adsorption performance of the carboxylic terminated Ti3C2Tx nanosheets synthesized using ammonium bifluoride and citric acid and applied as adsorbents for the removal of Cr(vi)and Pb(ii) from water. Adsorption efficiency was evaluated under sonication, MI concentration, and solution temperature at pH 5.5. Maximum adsorption capacities of 1090 mg g-1 and 1135 mg g-1 for Cr(vi) and Pb(ii) were attained within 7 and 4 minutes, respectively. Moreover, adsorption kinetic and isotherm studies were conducted, and the experimental data was found to fit well with pseudo-second-order reaction and Freundlich models. It was also established that the main interactions to drive the adsorption reactions were the electrostatic forces between the adsorbates and Ti3C2Tx adsorbent. Furthermore, (-COOH) and (-OH) terminal groups were the main contributors to the adsorption of Cr(vi) and Pb(ii) pollutants through an ion exchange mechanism. Besides the ion exchange mechanism, chemical coordination, entrapment of the adsorbates, and van der Waals forces lead to a physiochemical interaction between the MI and Ti3C2Tx nanosheets. In addition, Ti3C2Tx nanosheets showed better selectivity towards Pb(ii) removal than Cr(vi) in an aqueous solution. The nanosheets also exhibited more than 80% removal efficiency even after six cycles of regeneration and reusability. Additionally, Ti3C2Tx nanosheets offered superior adsorption performance for Cr(vi) and Pb(ii) compared to previously reported titanium carbide MXenes and activated carbon-based adsorbents. Hence, these high-quality and efficient Ti3C2Tx nanosheets can potentially eradicate other hazardous MI contaminants from wastewater.

A zeolitic imidazolate framework (ZIF-67) and graphitic carbon nitride (g-C3N4) composite based efficient electrocatalyst for overall water-splitting reaction.

Designing of non-noble, cost-effective, sustainable catalysts for water splitting is essential for hydrogen production. In this research work, ZIF-67, g-C3N4, and their composite (1, 3, 5, 6, 8 wt% g-C3N4@ZIF-67) are synthesized, and various techniques, XRD, FTIR, SEM, EDX and BET are used to examine their morphological properties for electrochemical water-splitting. The linkage of ZIF-67 with g-C3N4 synergistically improves the electrochemical kinetics. An appropriate integration of g-C3N4 in ZIF-67 MOF improves the charge transfer between the electrode and electrolyte and makes it a suitable option for electrochemical applications. In alkaline media, the composite of ZIF-67 MOF with g-C3N4 over a Ni-foam exhibits a superior catalyst activity for water splitting application. Significantly, the 3 wt% g-C3N4@ZIF67 composite material reveals remarkable results with low overpotential values of -176 mV@10 mA cm-2, 152 mV@10 mA cm-2 for HER and OER. The catalyst remained stable for 24 h without distortion. The 3 wt% composite also shows a commendable performance for overall water-splitting with a voltage yield of 1.34 v@10 mA cm-2. The low contact angle (54.4°) proves the electrocatalyst's hydrophilic nature. The results of electrochemical water splitting illustrated that 3 wt% g-C3N4@ZIF-67 is an electrically conductive, stable, and hydrophilic-nature catalyst and is suggested to be a promising candidate for electrochemical water-splitting application.

An inclusive review and perspective on Cu-based materials for electrochemical water splitting.

In recent years, there has been a resurgence of interest in developing green and renewable alternate energy sources as a solution to the energy and environmental problems produced by conventional fossil fuel use. As a very effective energy transporter, hydrogen (H2) is a possible candidate for the future energy supply. Hydrogen production by water splitting is a promising new energy option. Strong, efficient, and abundant catalysts are required for increasing the efficiency of the water splitting process. Cu-based materials as an electrocatalyst have shown promising results for application in the Hydrogen Evolution Reaction (HER) and Oxygen Evolution Reaction (OER) in water splitting. In this review, our aim is to cover the latest developments in the synthesis, characterisation, and electrochemical behaviour of Cu-based materials as a HER, and OER electrocatalyst, highlighting the impact that these advances have had on the field. It is intended that this review article will serve as a roadmap for developing novel, cost-effective electrocatalysts for electrochemical water splitting based on nanostructured materials with particular emphasis on Cu-based materials for electrocatalytic water splitting.

Enhancing the Overall Electrocatalytic Water-Splitting Efficiency of Mo2C Nanoparticles by Forming Hybrids with UiO-66 MOF.

For efficient electrocatalytic water-splitting, developing a nonprecious-metal-based stable and highly active material is the most challenging task. In this paper, we have devised a synthesis strategy for a hybrid catalyst composed of molybdenum carbide (Mo2C) and a Zr-based metal-organic framework (MOF) (UiO-66) via the solvothermal process. Synergistic effects between Mo2C and UiO-66 lead to a decrease in the hydrogen adsorption energy on the catalysts, and Mo2C/UiO-66 hybrids offer excellent catalytic activity in an alkaline environment for water-splitting. Particularly, the optimized Mo2C/UiO-66 hybrid, termed MCU-2 with 50:50 wt % of both components, displayed the best catalytic performance for both hydrogen and oxygen evolution reactions (HER/OER). It offered a small overpotential of 174.1 mV to attain a current density of 10 mA/cm2 and a Tafel plot value of 147 mV/dec for HER. It also offered a low overpotential of around 180 mV to attain a current density of 20 mA/cm2 and a Tafel plot value of 134 mV/dec for OER. Additionally, the catalyst was stable for over 24 h and ∼1000 cycles with a very minute shift in performance, and the electrolyzer indicates that a potential of ∼1.3 V is required to reach 10 mA/cm2 current density. It can be inferred from the results that the Mo2C/UiO-66 hybrid is a promising candidate as a nonexpensive and active catalyst for overall electrocatalytic water-splitting as the devised catalyst exhibits enhanced kinetics for both OER and HER, a more exposed surface area, faster electron transport, and enhanced diffusion of the electrolyte.

Nickel-Iron Nitride-Nickel Sulfide Composites for Oxygen Evolution Electrocatalysis.

Advance applications like water splitting system and rechargeable metal-air battery are highly dependent on efficient electrocatalyst for the oxygen evolution reaction (OER). Heterostructured materials, with a high active surface area and electron effect, accomplish enhanced catalytic performance. Here, a nitride-sulfide composite (FeNi3N-Ni3S2) has been prepared by a simple hydrothermal process coupled with nitridation. The prepared composite electrocatalyst FeNi3N-Ni3S2 possesses lower electron densities compared to those of FeNi3N and Ni3S2, lessening the activation energy (Ea) toward the OER. Consequently, the prepared FeNi3N-Ni3S2 exhibits excellent OER performance with a low overpotential (230 mV) and a small Tafel slope (38 mV dec-1). Highly stable FeNi3N-Ni3S2 composite delivers lower charging voltage and extended lifetime in rechargeable Zn-air battery, compared with IrO2.

Nanocomposites of NiO/CuO Based MOF with rGO: An Efficient and Robust Electrocatalyst for Methanol Oxidation Reaction in DMFC.

In this work a novel bimetallic nickel oxide/copper oxide metal-organic framework (NiO/CuO MOF) has been developed by using two linkers: Benzene Dicarboxylic acid (BDC) and Pyrazine. The composites of NiO/CuO MOF with different amounts of reduced graphene oxide (rGO) were synthesized through a hydrothermal method and subsequently characterized by multiple significant techniques like XRD, SEM, EDX, FTIR and Raman IR for an investigation of their structural and morphological properties. The prepared series of material was later employed for electrochemical oxidation of methanol, tested by cyclic voltammetry (CV) in basic medium on a modified glassy carbon electrode (GCE). The electrochemical response depicts that increasing concentration of rGO enhances the electrocatalytic activity of the catalyst for methanol oxidation reaction (MOR). The catalyzed oxidation reaction of methanol by NiO/CuO MOF and rGO-NiO/CuO MOF composites give a superlative current density of 437. 28 mA/cm2 at 0.9 V potential at 50 mV/s scan rate. This activity makes it a promising catalytic material for electrolysis of methanol in direct methanol fuel cell (DMFC).

Adsorption of CO2 on amine-functionalized green metal-organic framework: an interaction between amine and CO2 molecules.

The efficient capture of CO2 is a critical problem for porous adsorbents. The inadequacy of conventional adsorbents has low adsorption capacity towards CO2 removal. Metal organic frame work has been considered as very effective for CO2 adsorption as it shows higher rate of CO2 adsorption at room temperature. In conventional amine processes, a comparatively high energy penalty is required, whereas a novel class of metal-organic framework by the combination of amine solvent have improve the potential of adsorption process and also the efficiency of separation. Amine-functionalized MOFs become more fascinated due to strong interaction between carbon dioxide and amine-functionalized MOF. A renewable green γCD-MOF was synthesized by using vapor diffusion method. Post-synthetic modification of γCD-MOF was done with piperazine and analyzed to expose its crystalline structure, morphology, and porous structure. The main aim of this paper is to enhance the CO2 adsorption by functionalization of inexpensive, green, nanoporous γCD-MOF and also to highlight the effects of amine-based functionalization towards potential application. Gravimetric CO2 adsorption isotherms for γCD-MOF, pip-γCD-MOF are reported up to 60 °C and found to follow a pseudo-second-order reaction. The pip-γCD-MOF confirms comparatively increased rapid adsorption rate of CO2 than that of γCD-MOF and desorption of CO2, and need less energy for regeneration. These results are the complete evidence of piperazine as an efficient amine group for increasing the CO2 adsorption uptake capacity.

Nickel-Based Transition Metal Nitride Electrocatalysts for the Oxygen Evolution Reaction.

Electrocatalysis is an efficient and promising means of energy conversion, with minimal environmental footprint. To enhance reaction rates, catalysts are required to minimize overpotential. Alternatives to noble metal electrocatalysts are essential to address these needs on a large scale. In this context, transition metal nitride (TMN) nanoparticles have attracted much attention owing to their high catalytic activity, distinctive electronic structures, and enhanced surface morphologies. Nickel-based materials are an ideal choice for electrocatalysts given nickel's abundance and low cost in comparison to noble metals. In this Minireview, advancements made specifically in Ni-based binary and ternary TMNs as electrocatalysts for the oxygen evolution reaction (OER) are critically evaluated. When used as OER electrocatalysts, Ni-based nanomaterials with 3 D architectures on a suitable support (e.g., a foam support) speed up electron transfer as a result of well-oriented crystal structures and also assist intermediate diffusion, during reaction, of evolved gases. 2 D Ni-based nitride sheet materials synthesized without supports usually perform better than 3 D supported electrocatalysts. The focus of this Minireview is a systematic description of OER activity for state-of-the-art Ni-based nitrides as nanostructured electrocatalysts.

Highly integrated nanocomposites of RGO/TiO2 nanotubes for enhanced removal of microbes from water.

Highly integrated nanocomposite of Graphene oxide (GO) and its derivatives with metal oxides is essential for enhanced performance for various applications. Tuning the morphology is an important aspect during nanomaterials synthesis; this has an amplifying influence upon physicochemical properties of advanced functional materials. In this research work, GO/TiO2 nanotube composites have been successfully synthesized via alkaline hydrothermal treatment method by augmenting GO layers with two different phases of TiO2 (anatase and rutile) nanoparticles, followed by the hydrothermal treatment that also have caused reduction of GO to reduced GO (RGO). The morphology of the as-prepared samples appeared to be nanotubes with a large aspect ratio (length to diameter). The synthesized materials have been characterized using various techniques to determine their morphological and functional properties. Large surface area (158 m2/g) nanotube composites found accountable as effective disinfectant for water containing microorganisms. The antimicrobial activity of the synthesized composites was examined by disk diffusion method and optical density for bacterial growth using two different bacterial species; Escherichia Coli (E.coli, Gram-negative) and Staphylococcus Aureus (Methicillin-resistant Staphylococcus aureus, Gram-positive). The antibacterial study revealed that, the anatase phase RGO/TiO2 nanotube composites manifested appreciable effect on both bacteria as compared to rutile phase RGO/TiO2 nanotubecomposite.

Magnetic micro scavengers: highly porous Ni1-x Co x Fe2O4 microcubes for efficient disintegration of nitrophenol.

The fabrication of functional materials in patterned morphology is focused to obtain remarkable physiognomies of the materials for certain applications. Instead of randomly distributed agglomerated nanoparticles, it is highly desirable to arrange them in a motif, as this directed formation of nanomaterials can have a substantial influence on their performance and activity in various applications. With this perspective, MOF derived hollow cubes of nickel cobalt ferrites have been synthesized via a facile process using sacrificial templates at 600 °C. Microcubes, composed of tiny grains in a size range from 10 nm ± 2 nm were obtained in pure form as a polycrystalline material. The high specific surface area (1185 m2 g-1) and mesoporous nature of hollow cubic ferrites were found to be excellent adsorbents for nitrophenol at room temperature. The equilibrium quantity of adsorbed nitrophenol was calculated as 47 mg g-1 ferrite, accomplished in 7 min. Their large surface area, mesopores and hollow nature, in combination with controlled size distribution of grains, have enabled this remarkable utilization of nanoferrites for removal of nitrophenol from water.

Nitrogen doped RGO-Co3O4 nanograin cookies: highly porous and robust catalyst for removing nitrophenol from waste water.

The fabrication of nanograins with a uniform morphology wrapped with reduced graphene oxide (RGO) in a designed manner is critical for obtaining a large surface, high porosity and efficient catalytic ability at mild conditions. Hybrid structures of metal oxides decorated on two-dimensional (2D) RGO lacked an interface and channels between the individual grains and RGO. The present work focuses on the synthesis of RGO-wrapped Co3O4 nanograin architecture in micron-sized polyhedrons and the ability to reduce aromatic nitro compounds. Doping N in the designed microstructure polyhedrons resulted in very large surface area (1085.6 m2 g-1) and pore density (0.47 m3 g-1) microcages. Binding energies from x-ray photoelectron spectroscopy (XPS) and Raman intensities confirmed the presence of doped N and RGO-wrapped around Co3O4 nanograins. However, the morphology and microstructure was supported by FESEM and HRTEM images revealing the fabrication of high integrity RGO-Co3O4 microstructure hybrids composed of a 10 nm grain size with narrower grain size distribution. Ammonia treatment produced interconnected channels and dumbbell pores that facilitated ion exchange between the catalyst surface and the liquid medium at the grain boundary interfaces, and offered less mass transport resistance providing fast adsorption of reactants and desorption of the product causing surface renewal. Prepared N-RGO-Co3O4 shows the largest percentage reduction (96%) of p-nitrophenol (p-NP) at room temperature as compared to pure Co3O4 and RGO-Co3O4 nanograin microstructures over 10 min. Fabricated architectures can be applied effectively for fast and facile treatment of industrial waste streams with complex organic molecules.

Facile synthesis and enhanced photocatalytic activity of single-crystalline nanohybrids for the removal of organic pollutants.

This study focused on the synthesis of α-MoO3/rGO (rGO, reduced graphene oxide). One-dimensional nanohybrids under mild conditions and a low temperature wet chemical route produced highly pure single-crystalline orthorhombic α-MoO3 on GO sheets. Four nanohybrids, labeled as GMO-0, GMO-1, GMO-2 and GMO-3, were synthesized with different mass chargings of GO (0 mg, 40 mg, 60 mg and 100 mg, respectively). The photocatalytic performance for reduction of organic pollutants was analyzed. The presence of different amounts of GO in the prepared metal oxide hybrids altered the performance of the material as elaborated by the Brunauer-Emmett-Teller surface area, UV-visible diffuse reflectance spectra and the resulting reduction of organic dyes depicted by photocatalytic experiments. GO as a support material and active co-catalyst decreased the band gap of α-MoO3 (2.82 eV) to lower values (2.51 eV), rendering the prepared hybrids usable for visible-light-induced photocatalysis. The large specific surface area (72 m2 g-1) of the mesoporous α-MoO3/rGO nanohybrid made it an efficient photocatalyst for the elimination of azo dyes. Very fast reduction (100%) of Rhodamine B was observed in a few minutes, while Congo Red was degraded by 76% in 10 min, leading to the formation of stable intermediates that were completely neutralized in 12-14 h under light irradiation. The amount of GO loaded in the samples was limited to a point to achieve better results. After that, increasing the amount of GO decreased the extent of degradation due to the presence of a higher electron acceptor. Photocatalytic experiments revealed the synergistic effect, high selectivity of the prepared nanohybrids and degradation of azo dyes. The kinetics of the degradation reaction were studied and found to follow a pseudo first-order reaction.