Formation Of Crystalline Phases Research Articles

Low-temperature oxidative dehydrogenation of propane over NiV mixed oxides derived from LDH precursors

A series of NiV mixed metal oxide (MMO) catalysts were derived from the NiV layered double hydroxides (LDHs) synthesized by the constant pH coprecipitation method. The synthesis parameters, (i) Ni/V molar ratio and (ii) calcination temperature ( Tp), were controlled. The MMO catalysts were characterized by physicochemical characterization techniques and then tested for the oxidative dehydrogenation of propane (ODHP). The results showed that the calcination temperature affected the crystalline phase formation and grain size of NiO, as well as the activated temperature of propane, and the addition of V greatly regulated the activity and quantity of the surface oxygen species and improved the propylene selectivity. 4NiV-500 catalyst (Ni/V = 4, Tp = 500 °C) exhibited the best catalytic performance at low temperature (250 °C) with an initial propylene selectivity of about 70%. Therefore, it is an effective method to obtain NiV MMO catalysts with excellent low-temperature activity for ODHP, using LDHs as the precursors while controlling the appropriate amount of V and calcination temperature simultaneously.

Effective role of vibrational annealing in enhancing room temperature physical properties of Co doped ZnO nanoparticles by using novel TVA technique

Well-annealed nanocrystalline semiconductor materials in pellet or thin film form, composed of small grains with a high surface-to-volume ratio, are considered as promising candidates for multiple device applications. However, no such method is available yet that can control the grain size of such samples during heat treatment. In this present work, a novel thermo-vibrational annealing (TVA) setup for processing nanocrystalline materials was designed and fabricated in-house. Here both thermal and mechanical vibrational energy were simultaneously applied to the sample during annealing, followed by vibrational dry quenching in the presence of an inert gas environment. Co-doped ZnO pellets were synthesized by chemical route pyrophoric method followed by annealing at 800 °C for 4 h using this set up. For comparison, one pellet was annealed with vibration with calibrated vibration at a speed of 360 rpm, and another pellet was annealed without vibration. X-ray diffraction (XRD), Raman and Fourier transform Infrared (FTIR) spectroscopic studies showed the formation of a single crystalline phase with hexagonal wurtzite structure of both the samples and the proper incorporation of Co2+ ions into the ZnO matrix without any impurity phases, which was also confirmed by energy dispersive X-ray (EDX) spectroscopy studies. Scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM) studies confirmed the decrease in average grain and particle size of the sample when processed with the TVA setup. Ultraviolet–Visible spectra showed that the bandgap energy of the Co-doped ZnO sample varies inversely with particle size. Hall-effect measurements demonstrated the semiconducting nature of both samples with n-type charge carriers. The presence of Co2+ ions in the wurtzite ZnO lattice was confirmed by X-ray photoelectron spectroscopy (XPS). The magnetic properties were studied using a SQUID magnetometer, which confirmed that a Co doped ZnO sample annealed with the TVA technique exhibit better room temperature ferromagnetism properties compared to sample annealed without vibration. Based on these studies, it was believed that the sample annealed by mechanical vibrational energy with vibrational dry quenching has a great influence on several physical properties of any material and hence Co doped ZnO sample processed with this TVA technique can be used as a promising candidate for multiple sensor and magnetic storage devices.

Ceramic matrix piezocomposites: method of fabrication and microstructure peculiarities

In the present work, we have developed a new method for the fabrication of piezoactive ceramic matrix composites (CMC) ceramics/ceramics. Samples of piezoactive PZT/PZT composites with a mass concentration of components from 0% to 60% have been obtained. A study of microstructural features, as well as a gravimetric analysis of CMC, has been carried out. It has been shown that the developed method for CMC manufacturing provides the formation of microhomogeneous composite structures with a uniform distribution of ceramic filler particles in a microporous piezoceramic matrix without the formation of transition regions and additional crystalline phases.

Eco-Friendly Synthesis of Ni/NiO Nanoparticles Using Gymnema sylvestre Leaves Extract for Antifungal Activity

The invention of an easy synthetic approach for extremely impactful nanomaterials (NMs) is one of the crucial research areas in modern science and engineering. In the present work, we describe a cost-effective, simple, rapid and environmentally gracious biogenic fabrication of nickel/nickel oxide nanoparticles (Ni/NiO NPs) using Gymnema sylvestre as a natural fuel. The textural characteristics of as-prepared Ni/NiO NPs were explored using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), diffuse reflectance spectra (DRS), photoluminescence spectroscopy (PL), field-emission scanning electron microscope (FESEM), energy dispersive X-ray analysis (EDX), and high-resolution transmission electron microscopy (HRTEM). XRD affirmed the crystalline nature and phase formation of Ni/NiO NPs. The FTIR spectrum ascertains the formation of Ni/NiO NPs, and the band gap of 4.29 eV is revealed from DRS studies. Ni/NiO NPs display an intense emission peak at 576.2 nm in their PL spectrum. The fabrication of pseudo-spherical Ni/NiO NPs was displayed by FESEM and HRTEM images. The particle size obtained from HRTEM was 21 nm, which resembles the median crystallite size ascertained from the XRD data. Additionally, the plausible mechanism for Ni/NiO NPs formation is illustrated. Moreover, as-synthesized Ni/NiO NPs displayed considerable antifungal potential against Candida albicans and Aspergillus niger. Results revealed that the Gymnema sylvestre leaves extract can synthesize Ni/NiO NPs with appealing biological effectiveness for application in the nanomedicine sector.

Formation of Porous Structures and Crystalline Phases in Poly(vinylidene fluoride) Membranes Prepared with Nonsolvent-Induced Phase Separation—Roles of Solvent Polarity

PVDF membranes were prepared with nonsolvent-induced phase separation, using solvents with various dipole moments, including HMPA, NMP, DMAc and TEP. Both the fraction of the polar crystalline phase and the water permeability of the prepared membrane increased monotonously with an increasing solvent dipole moment. FTIR/ATR analyses were conducted at the surfaces of the cast films during membrane formation to provide information on if the solvents were present as the PVDF crystallized. The results reveal that, with HMPA, NMP or DMAc being used to dissolve PVDF, a solvent with a higher dipole moment resulted in a lower solvent removal rate from the cast film, because the viscosity of the casting solution was higher. The lower solvent removal rate allowed a higher solvent concentration on the surface of the cast film, leading to a more porous surface and longer solvent-governed crystallization. Because of its low polarity, TEP induced non-polar crystals and had a low affinity for water, accounting for the low water permeability and the low fraction of polar crystals with TEP as the solvent. The results provide insight into how the membrane structure on a molecular scale (related to the crystalline phase) and nanoscale (related to water permeability) was related to and influenced by solvent polarity and its removal rate during membrane formation.

Microstructure and gyromagnetic properties of low-sintered LiZnTi ferrite doped with nano-LiZn and V2O5 additives

In this study, nanoparticles of LiZn ferrite (nano-LiZn, 0.0–10.0 wt. %) fabricated via the sol-gel method and V2O5 particles were added into a Li0.43Zn0.27Ti0.13Fe2.17O4 (LiZnTi) ferrite to realize low temperature sintering. The effects of the nano-LiZn ferrite addition on the crystalline phase formation, microstructure, and magnetic properties of LiZnTi ferrite were systematically investigated. X-ray diffraction results reveal that the LiZnTi ferrite doped with nano-LiZn and V2O5 additives present a pure spinel structure, which can be explained by liquid phase of V2O5 and spinel structure of nano-LiZn, as revealed by high-resolution transmission electron microscopy and selected area electron diffraction data. Scanning electron microscopy images show that the addition of nano-LiZn leads to a change in the microstructure, with the grains becoming uniform and dense. Additionally, the variation in the saturation magnetization (Ms) depends on the LiZn content. In particular, Ms increases with increasing LiZn content from 2.0 to 10.0 wt. %. Finally, the LiZnTi ferrite doped 4.0 wt. % nano-LiZn and 0.60 wt. % V2O5 possesses a narrow ferromagnetic resonance linewidth of 197 Oe, a reduced coercivity of 192.6 A/m, and an improved bulk density of 4.73 g/cm3.

Study of Carbonated Clay-Based Phosphate Geopolymer: Effect of Calcite and Calcination Temperature

This study aims to use natural carbonated Tunisian clay as an aluminosilicate precursor for the elaboration of phosphate-based geopolymers, which yields to the valorization of this common material in Tunisia. In addition, the presence of calcium carbonate in this clay allows the investigation of this associated mineral’s effect on the properties of geopolymeric materials. To achieve these purposes, several experimental techniques were used, namely fluorescence (FX), particle size analysis, thermogravimetric analysis (TGA), differential thermal analysis (DTA), dilatometric analysis, X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). The mechanical strength and the open porosity of the obtained geopolymeric samples were tested by the compression test and the standard test method for water absorption, respectively. The findings of this work show that the used Tunisian clay can present an attractive aluminosilicate precursor for the synthesis of phosphate-based geopolymers. It also shows that the chosen calcination temperature of the raw clay considerably modifies the reactivity of minerals during geopolymerization and, consequently, strongly affects the properties and structure of the geopolymeric samples. These effects were attributed essentially to the formation of new calcium crystalline phases in the obtained geopolymeric samples. In fact, the anorthite (CaAl2Si2O8) phase appears in all the samples but in greater abundance in those obtained from the clay calcined at 550 °C, and the brushite phase (CaHPO4·2H2O) appears only in the samples obtained from the clay calcined at 950 °C. All these new crystalline phases are strongly dependent on the state of the calcite present in the calcined clay.

Electrodeposition of Ni−Rh Alloys and their Use as Cathodes for Nitrate Reduction in Alkaline Solutions

AbstractCompact Ni−Rh alloys are electrodeposited potentiostatically on rotating disk and sheet electrodes; film compositions are adjusted by varying bath composition and deposition potential Edep. SEM images of these alloys show a compact, globular morphology for Rh contents up to 30 at%, and a smoother aspect for films with a medium‐to‐high content of Rh. XRD spectra show the formation of a single crystalline phase, with diffraction peaks in intermediate positions between those of the constituent elements. Data analysis indicates that crystal lattice parameters vary with composition according to Vegard's law. Linear voltammetries of nitrate reduction in alkali highlight a maximum of activity, in terms of reduction current, for alloys in the range of 10–30 at.% Rh. Prolonged electrolysis at appropriate potential performed with Ni85Rh15 alloy shows, in comparison with pure Ni and pure Rh: much increased activity and faster abatement of nitrate; lower production of the undesired nitrite species; higher selectivity towards production of ammonia.

Controlled Release of H2S from Biomimetic Silk Fibroin-PLGA Multilayer Electrospun Scaffolds.

The possibility of incorporating H2S slow-release donors inside biomimetic scaffolds can pave the way to new approaches in the field of tissue regeneration and anti-inflammatory treatment. In the present work, GYY4137, an easy-to-handle commercially available Lawesson's reagent derivative, has been successfully incorporated inside biomimetic silk fibroin-based electrospun scaffolds. Due to the instability of GYY4137 in the solvent needed to prepare silk fibroin solutions (formic acid), the electrospinning of the donor together with the silk fibroin turned out to be impossible. Therefore, a multilayer structure was realized, consisting of a PLGA mat containing GYY4137 sandwiched between two silk fibroin nanofibrous layers. Before their use in the multilayer scaffold, the silk fibroin mats were treated in ethanol to induce crystalline phase formation, which conferred water-resistance and biomimetic properties. The morphological, thermal, and chemical properties of the obtained scaffolds were thoroughly characterized by SEM, TGA, DSC, FTIR, and WAXD. Multilayer devices showing two different concentrations of the H2S donor, i.e., 2 and 5% w/w with respect to the weight of PLGA, were analyzed to study their H2S release and biological properties, and the results were compared with those of the sample not containing GYY4137. The H2S release analysis was carried out according to an "ad-hoc" designed procedure based on a validated high-performance liquid chromatography method. The proposed analytical approach demonstrated the slow-release kinetics of H2S from the multilayer scaffolds and its tunability by acting on the donor's concentration inside the PLGA nanofibers. Finally, the devices were tested in biological assays using bone marrow-derived mesenchymal stromal cells showing the capacity to support cell spreading throughout the scaffold and prevent cytotoxicity effects in serum starvation conditions. The resulting devices can be exploited for applications in the tissue engineering field since they combine the advantages of controlled H2S release kinetics and the biomimetic properties of silk fibroin nanofibers.

Aligned TiO2 Scaffolds in the Presence of a Galactopyranose Matrix by Sol-Gel Process.

In this work, titanium dioxide scaffolds were synthesized. Titanium isopropoxide (IV) was used as a precursor in its formation, using a polymeric network of galactopyranose as a template. The powder sample obtained was evaluated by scanning tunneling microscopy (STM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) analysis, and thermal gravimetric analysis (TGA-DTA). According to the results, it was found that these scaffolds can be successfully synthesized in solution using the sol-gel method. The synthesized scaffolds have diameters from 50 nm with porosity of approximately 0.3-10 nm. Important parameters, such as pH and the concentration of the metallic precursors, were optimized in this solution. The values of maximum average roughness R(max) and roughness value (Ra) were 0.50 and 1.45, respectively. XRD diffraction analysis shows the formation of crystalline phases in the TiO2 scaffold at 700 °C. The use of biological polymers represents an alternative for the synthesis of new materials at low cost, manipulating the conditions in the production processes and making the proposed system more efficient.

Плазмохимическое модифицирование стеклокремнезита на основе отходов обогащения железистых кварцитов КМА

Based on the conducted research, it is proposed to use the waste of the enrichment of ferruginous quartzites of KMA as the main raw material for the production of fire-filtered glass silica. The regularities of the formation of the phase composition of glass silica with the formation of such crystalline phases as hematite and hypersthene are established. Based on experimental studies using X–ray phase, differential thermal analysis and IR spectroscopy, a mechanism for the formation of the phase composition of glass silica is proposed. The advantages of the developed technology in comparison with analogues are shown. It was found that after plasma chemical modification, such performance indicators of the front surface of glass silica as water resistance, acid resistance, alkali resistance and hardness significantly increase.

МОДЕРНИЗАЦИЯ ТЕХНОЛОГИЧЕСКИХ ПРОЦЕССОВ ИЗГОТОВЛЕНИЯ АЛКОЗОЛЯ WO3

Alkosol WO3 is used for the production of functional nanocoatings that exhibit electrochromic effect. These nanocoatings have a wide range of applications, but the most promising and economically feasible is their use in the structure of architectural "smart" windows to regulate the passing light and heat flows. Practical application of electrochromic windows will allow to reduce electric energy losses for heating and cooling of buildings and vehicles up to 40%. This article is devoted to the description of the developed technological approaches for the production of WO3 alcosol by the peroxide method. Modernization of the technological process of manufacturing this material made it possible to minimize the formation of a side insoluble crystalline phase of H2WO5, to automate the process of polycondensation of peroxotungstic acid, to obtain a WO3•nH2O2•mH2O hydrogel of a uniform composition, and to accelerate the dissolution of the hydrogel in ethanol from 12 hours to 5 minutes. The total time of all stages of the technological process for the production of alcosol WO3 was reduced from 3 days to 8 hours.

Transformation of mineral matter during pyrolysis, gasification and combustion of biosolid chars

During thermochemical processing of biosolids in sewage sludge, different forms of phosphorus-containing compounds are generated in biosolid chars (biochars). This study examines the effects of biochar processing conditions on the mineral compounds produced during the pyrolysis, gasification, and combustion of biosolids, and the major determinants of phase formation kinetics. Our results show identified phase transformations through experiments in a laboratory tube furnace followed by X-ray diffraction analysis (XRD). Additionally, a synchrotron powder diffraction study was conducted to verify XRD results of the laboratory processed samples and to observe in situ phase transformations in biochars. It was found that under a neutral atmosphere, crystalline oxide phases are formed at lower temperatures and much faster than iron phosphide, while gasification and combustion conditions led to the formation of crystalline phases in phosphate forms. These forms of phosphorus compounds in by-products of biosolids thermochemical treatment can be used as agricultural fertilizers.

Sintering Property and Hydration Resistance of CaO-Y2O3 Composite Materials

A preparation method of CaO-Y2O3 composite materials and its sintering property and hydration resistance were investigated in this paper. The CaO-Y2O3 core-shell structure powders were obtained by precipitation, after calcination, pressing and sintering the CaO-Y2O3 composite materials were prepared. The obtained powders and composite materials were characterized by crystalline phase formation, thermodynamic property, density, hydration resistance and microstructural analysis. The results showed that the prepared CaO-Y2O3 core-shell structure powders had good coating property, the sintering property and hydration resistance of composite materials were excellent. As the molar ratio Ca to Y was 1:1, the relative bulk density was 95.68%, the apparent porosity was 1.28%, and the hydration weight gain rate of the sample after 21 days in the atmospheric environment was 0.45%.

Investigation of structure and properties of melt-spun NiTi based shape memory alloys

In this work, we investigated the structure, mechanical properties and corrosion resistance of Ti50Ni50 and Ti16.667Zr16.667A16.667Ni25Cu25 (A = Hf, Nb, Co, Cr and Ga) shape memory alloys (SMAs) fabricated by using melt-spinning method. X-ray diffraction (XRD) and scanning electron microscopy (SEM) analyses reveal that the alloy ribbons are partially crystallized with B19' martensitic structure in the added alloys. The crystalline phase formation and the atomic size difference (δ = 4.33 - 10.25%) significantly affect the hardness, tensile strength, tensile strain, elastic modulus and corrosion resistance of the alloys. The hardness of the alloy gradually increases from 583 HV to 873 HV when adding elements in the order of Hf, Nb, Co, Cr and Ga. Tensile strength, tensile strain and elastic modulus simultaneously reach their maximum of 669.2 MPa, 0.899% and 28.82 GPa, respectively, when Hf is added to the alloy. Ga enhances the corrosion resistance of the alloy ribbons more than other additional elements.

Significant improvement in surface hardness of Zr-based metallic glass by nanosecond pulsed laser irradiation in graphite powder water suspension

Metallic glasses (MGs) have shown promising application prospects as structural materials due to their unique mechanical properties. While, for broadening their application as functional materials, significant improvement in surface hardness of MGs is required. Accordingly, in this study, laser carbonization of MGs was attempted by irradiating the Zr-based MG surface immersed in graphite powder water suspension using a nanosecond pulsed laser. Nanoindentation response and surface morphologies of the initial and irradiated surfaces were characterized in detail. The results indicated that the hardness of the laser-irradiated surfaces was increased by 130 %–200 % (from 6.407 GPa to 19.193 GPa), and as well, the serrated flows in load-depth curves and the surface shear bands around the residual indent disappeared, suggesting the change in micro-scale plastic deformation behaviors of the laser-irradiated surfaces. Furthermore, the chemical composition of the initial and irradiated surfaces was analyzed by X-ray diffraction (XRD) and energy dispersive spectrometer (EDS), which showed that the irradiated surfaces were carbonized in the graphite powder water suspension. Accordingly, the increase in surface hardness was due to the formation of the hard crystalline phases.

Plasma Jet Sputtering as an Efficient Method for the Deposition of Nickel and Cobalt Mixed Oxides on Stainless-Steel Meshes: Application to VOC Oxidation

Hollow cathode plasma sputtering is an advantageous method of preparing catalysts in the form of thin oxide films on supports. Such catalysts are particularly suitable for processes such as catalytic total oxidation of volatile organic compounds (VOCs), representing an economically feasible and environmentally friendly method of VOC abatement. Catalysts with Ni:Co molar ratios of 1:4, 1:1, and 4:1 were prepared on stainless-steel meshes and compared with single-component Ni and Co oxide catalysts. The properties of the catalysts were characterized by EDX, SEM, powder XRD, temperature-programmed reduction (H2-TPR), Raman spectroscopy, and XPS. Powder XRD revealed the formation of various crystalline phases that were dependent on molar the Ni:Co ratio. NiO and Co3O4 were identified in the single-component Ni and Co oxide catalysts, whereas Ni-Co mixed oxides with a spinel structure, together with NiO, were found in the catalysts containing both Ni and Co. Raman spectra of the catalysts prepared at high working pressures showed a slightly lower intensity of bands, indicating the presence of smaller oxide particles. The TPR profiles confirmed the improved reducibility of the Ni-Co oxide catalysts compared to the single-component Ni and Co catalysts. Catalytic activity was investigated in the deep oxidation of ethanol and toluene, which were used as model volatile organic compounds. In ethanol oxidation, the activity of sputtered catalysts was up to 16 times higher than that of the commercial Cu-Mn oxide catalyst EnviCat® VOC-1544. The main benefits of the sputtered catalysts are the much lower content of Ni and Co oxides and a negligible effect of internal diffusion. Moreover, the process of plasma jet sputtering can be easily implemented on a large scale.

Effect of Thermal Treatment on the Structure and Morphology of Vanadium Doped ZnO Nanostructures Obtained by Microwave Assisted Sol-Gel Method.

In this paper, we conducted a fundamental study concerning the effect of thermal treatment on the structure and morphology of 2 mol% vanadium doped ZnO nanopowders obtained by microwave assisted sol-gel method (MW). The samples were analyzed by DTA, FTIR, XRD, SEM, and UV-Vis spectroscopy. The DTA results showed that above 500 °C, there was no mass loss in the TG curves, and ZnO crystallization occurred. The XRD patterns of the thermally treated powders at 500 °C and 650 °C showed the crystallization of ZnO (zincite) belonging to the wurtzite-type structure. It was found that in the 650 °C thermally treated powder, aside from ZnO, traces of Zn3(VO4)2 existed. FTIR spectra of the annealed samples confirmed the formation of the ZnO crystalline phase and V-O bands. The micrographs revealed that the temperature influenced the morphology. The increase in the annealing temperature led to the grain growth. The SEM images of the MW powder thermally treated at 650 °C showed two types of grains: hexagonal grains and cylindrical nanorods. UV-Vis spectra showed that the absorption band also increased with the increasing temperature of thermal treatment. The MW sample annealed at 650 °C had the highest absorption in ultraviolet domain.

Crystallization of Aluminum droplet at low undercooling: homogeneous nucleation approach

Crystallization in an undercooled Aluminum (Al) droplet occurs via the formation of crystalline nuclei by homogeneous or heterogeneous nucleation and successive growth of nuclei. Clusters of a new phase appear in the system due to fluctuations and after reaching a critical size grow up to microscopic size. Crystallization event at low undercooling 6.4°C of 9.91 mg in compact Al sample was detected using isothermal differential scanning calorimetry (DSC) after several tenths of minutes. In this case, standard analysis based on Johnson-Mehl-Avrami-Kolmogorov (JMAK) model is not appropriate as Avrami parameter n obtained by fitting of DSC data is too low (n ≤ 1 and thus the dimensionality of the system d = n – 1 ≤ 0). Al growth rate is extremely high and that is why we presume that the time delay of crystallization, detected by DSC, is slightly higher than nucleation time delay. A homogeneous nucleation model is applied to determine the basic characteristics of nucleation: the size distribution of nuclei, nucleation rate, total number of nuclei and crystallization fraction at the nucleation process. The number of atoms in a liquid Aluminum droplet decreases with time as the formation of a new crystalline phase occurs. As a consequence, a decrease in stationary nucleation occurs. It is shown that decrease in the number of atoms in a liquid Al droplet is predominantly caused by formation of subcritical clusters.

Pharmaceutical Co-crystal of Antiviral Agent Efavirenz with Nicotinamide for the Enhancement of Solubility, Physicochemical Stability, and Oral Bioavailability.

The present research work attempted to improve the oral bioavailability of the antiviral drug Efavirenz (EFV) using a pharmaceutical cocrystallization technique. EFV comes under BCS-II and has extremely low water solubility, and results in low oral bioavailability. EFV and nicotinamide (NICO) were selected in a (1:1) stoichiometric ratio and efavirenz nicotinamide cocrystal (ENCOC) was prepared through the liquid-assisted grinding method (LAG). The confirmation of the formation of a new solid phase was done through spectroscopic techniques like Fourier transmission infrared (FTIR), Raman, and 13C solid-state nuclear magnetic resonance (13C ssNMR). Thermal techniques like differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and hot stage microscopy (HSM) illustrated the thermal behavior and melting patterns of ENCOC, EFV, and NICO. The X-ray powder diffraction (XRPD) confirms the formation of a new crystalline phase in ENCOC. The Morphology was determined through scanning electron microscopy (FESEM). The results of saturated solubility studies andin vitro drug release studies exhibited 8.9-fold enhancement in solubility and 2.56-fold enhancement in percentage cumulative drug release. The percentage drug content of ENCOC was found higher than 97% and cocrystal exhibits excellent accelerated stability. The oral bioavailability of EFV (Cmax, 799.08ng/mL) exhibits significant enhancement after cocrystallization (Cmax, 5597.09ng/mL) than EFV and Efcure®-200 tablet (2896.21ng/mL). The current work investigates the scalable and cost-effective method for enhancement of physicochemical stability, solubility, and oral bioavailability of an antiviral agent EFV.