Intermediate Phase Research Articles

Microscopic pathways of transition from low-density to high-density amorphous phase of water.

In recent years, much attention has been devoted to understanding the pathways of phase transition between two equilibrium condensed phases (such as liquids and solids). However, the microscopic pathways of transition involving non-equilibrium, non-diffusive amorphous (glassy) phases still remain poorly understood. In this work, we have employed computer simulations, persistence homology (a tool rooted in topological data analysis), and machine learning to probe the microscopic pathway of pressure-induced non-equilibrium transition between the low- and high-density amorphous (LDA and HDA, respectively) ice phases of the TIP4P/2005 and ST2 water models. Using persistence homology and machine learning, we introduced a new order parameter that unambiguously identifies the LDA- and HDA-like local environments. The LDA phase transitions continuously and collectively into the corresponding HDA phase via a pre-ordered intermediate phase during the isothermal compression. The local order parameter susceptibilities show a maximum near the transition pressure (P*)-suggesting maximum structural heterogeneities near P*. The HDA-like clusters are structurally ramified and spatially delocalized inside the LDA phase near the transition pressure. We also found manifestations of the first-order low-density to high-density liquid transition in the sharpness of the order parameter change during the LDA to HDA transition. We further investigated the (geometrical) structures and topologies of the LDA and HDA ices formed via different protocols and also studied the dependence of the (microscopic) pathway of phase transition on the protocol followed to prepare the initial LDA phase. Finally, the method adopted here to study the phase transition pathways is not restricted to the system under consideration and provides a robust way of probing phase transition pathways involving any two condensed phases at both equilibrium and out-of-equilibrium conditions.

Effect of arsenate and phosphate substitution on hydroxyl group in libethenite Cu2PO4OH - olivenite Cu2AsO4OH solid solution series

Libethenite and olivenite have been regarded as intriguing photocatalysts because of their singular structures. Copper hydroxy-phosphates and -arsenates exhibit distinctive properties: they incorporate bridging hydroxyl (OH) groups shared by neighboring copper atoms. In materials employed for photoelectrochemical applications, the significance of surface OH groups and OH-related defects frequently varies and is contingent upon the specific material system and the reaction under consideration. Hydroxyl groups can enhance photocatalytic performance by generating OH radicals or serving as crucial agents in catalytic reactions. Therefore, the presence of an OH group within the crystal structure of the material can give rise to potentially interesting behaviors. Seven compounds within the solid solution series of libethenite Cu2PO4OH and olivenite Cu2AsO4OH with stoichiometric ratio (Cu2(Px,As1- xO4)OH, x = 0, 0.1, 0.3, 0.5, 0.7, 0.9, 1 were synthesized at 70 °C via aqueous solutions, and their properties were examined using X-ray diffraction (XRD), Scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS), Fourier-transform infrared spectroscopy (FTIR) and Raman spectroscopy. The effect of substituting (PO4)3– ions with (AsO4)3– ions on the alteration of the lattice parameters and spectral characteristics was elucidated by analyzing the correlation between the chemical composition and X-Ray diffraction peak positions. The substitution process leads to modifications in the unit cell parameters and volume. These isomorphic substitutions can be also discerned through alterations in the infrared and Raman spectra, which exhibit variations in the position and intensity of the bands corresponding to phosphates, arsenates, and hydroxyl ions. The incorporation of As into the solid solution resulted in altered bond lengths and geometries, which is consistent with the symmetry transition from orthorhombic libethenite to monoclinic olivenite. The variations in the unit cell parameters and the shifts in the peak position exhibited non-linear trends, and a discernible step was observed between the Cu2(P0·3As0.7)O4OH and Cu2(P0·5As0.5)O4OH intermediate phases. The findings of this study will prove beneficial in evaluating the feasibility of the libethenite-olivenite isometric series as a photocatalysts.

Investigation of membrane fouling behaviors triggered by different characteristics of anaerobic digestion effluent in membrane distillation

This study investigated the membrane fouling behaviors triggered by different characteristics of anaerobic digestion (AD) effluents in the operation of 851-h membrane distillation (MD). The AD effluents with different concentration factors (CF) were used as the feed separately. Results illustrated a stable normalized water flux in the treatment of raw AD effluent (CF = 1) over the 851-h MD experiment, showing negligible membrane fouling. While the sharp decreases in normalized water flux occurred when treating the concentrated AD effluents. The membrane fouling mechanism tended to change from inorganic scaling to organic fouling when the CF value increased from 1 to 3, while the combination of organic and inorganic fouling dominated the membrane fouling when CF was 5. Inorganic fouling was further intensified when the CF value increased to 10. The regression analysis demonstrated that the complete blocking model was the dominant development mechanism for CF = 3 treatment. The membrane fouling mechanism of CF = 5 treatment switched from the cake filtration model in the intermediate phase to the standard blocking model in the final phase. Additionally, there was a transition from the complete blocking model to the standard blocking model for CF = 10 treatment. The study may provide an in-depth knowledge of membrane fouling control during the actual AD effluent concentrating process.

Nanosized Tungsten Powder Synthesized Using the Nitridation–Decomposition Method

A facile, one-step nitridation–decomposition method was developed for the synthesis of nanosized tungsten powder with a high surface area. This approach involved the nitridation of WO3 in NH3 to form mesoporous tungsten nitride (W2N), followed by in situ decomposition of W2N to directly yield single-phase W particles. The phase and morphology evolution during the synthesis were systematically investigated and compared with the carbothermal reduction of WO3. It was revealed that powdered tungsten product with single-phase particles was obtained after nitridation at 800 °C combined with in situ decomposition at 1000 °C, displaying an average particle size of 15 nm and a large specific surface area of 6.52 m2/g. Furthermore, the proposed method avoided the limitations associated with intermediate phase formation and coarsening observed in carbothermal reduction, which resulted in the growth of W particles up to ~4.4 μm in size. This work demonstrates the potential of the nitridation–decomposition approach for the scalable and efficient synthesis of high-quality, fine-grained tungsten powder.

Mathematics in South Africa’s Intermediate Phase: Music integration for enhanced learning

Background: Embracing the influential role of music in education, teachers an cultivate an environment that fosters learners’ curiosity, creativity, and enthusiasm for acquiring knowledge. The first author, experienced in teaching Intermediate Phase music and mathematics, was keen to explore how to bridge the gap between the educational vision for 21st-century knowledge and skills and current teaching practices through the adoption of active music integration and appropriate pedagogy to full engage learners.Aim: The study aimed to explore how general teachers, with no previous formal music exposure perceived and engaged with the process of correlating concepts and learning experiences in music and mathematics.Setting: The research was conducted over nine weeks in three South African, Afrikaans-medium, middle-class governmental primary schools located in the Tshwane North district of the Gauteng province.Methods: This study employed a qualitative case study research approach and was situated within the pedagogical design of constructive alignment for effective teaching and learning.Results: The results underscore the significance of generalist teachers’ ability to effectively incorporate music into mathematics lessons without extensive musical training or instrumental skills.Conclusion: The article challenges the notion that musical expertise is a prerequisite for integration, highlighting the fact that generalist teachers can successfully incorporate music into mathematics instruction by fostering meaningful connections between the two subjects.Contribution: This article draws attention to the importance of constructive alignment in promoting independent thinking and the practical application of knowledge. These findings offer guidance for the development of pedagogical frameworks and instructional practices that prioritise meaningful teaching and learning experiences.

Multiple intermediate phases in the interpolating Aubry-André-Fibonacci model

Multiple intermediate phases in the interpolating Aubry-André-Fibonacci model

Orientation-dependent deformation mechanisms of alpha-uranium single crystals under shock compression

Large-scale non-equilibrium molecular dynamics (NEMD) simulations were employed to investigate the dynamic deformations of alpha-uranium (α-U) single crystals subjected to varying shock strengths along low-index crystallographic orientations. The pronounced anisotropy of α-U gives rise to a complex microstructural evolution under shock loading. In-depth microstructural analysis of post-shock specimens reveals the identification of multiple dynamic deformation mechanisms. Notably, when the shock loading direction aligns with the a-axis, dynamic deformation of the α-U single crystals is primarily dominated by lattice instability, which attributes to a crystalline-to-amorphous transition serving as the dominant shear stress relaxation pathway. On the other hand, shock loading along the b-axis results in an abundance of deformation twins, with twinning planes identified as (130) and (13¯0). During the twinning event, the α-U matrix undergoes a transition to a metastable intermediate phase, subsequently decomposing into a composite structure comprising α-U twins and matrix. This unconventional twinning mechanism significantly deviates from classical theories. Furthermore, upon loading along the c-axis, twinning and a phase transition from α-U to body-centered tetragonal phase (bct-U) occur in α-U single crystal samples. Given that the pressure threshold of this phase transition predicted by ab initio calculations is as high as ∼270 GPa, the phase transition from α-U to bct-U might be implausible. An alternative interatomic potential of uranium with the higher pressure threshold was employed to reinvestigate the shock response of α-U single crystals along the c-axis. The phase transition of α-U to bct-U disappears, and twinning dominates the plastic deformation, with the twinning orientation conforming to the {112} twinning. The strong anisotropy of the α-U lattice triggers a wealth of orientation-dependent dynamic deformation mechanisms. The activation of the twinning system is evidently associated with the loading direction, constituting the potential cause for the discovery of multiple twinning variants during the deformation in polycrystalline uranium.

X-ray spectral properties of dust-obscured galaxies in the XMM-SERVS coverage of the XMM-LSS field

ABSTRACT With an aim to unveil the population of obscured active galactic nuclei (AGN) hosted in high-z dust-obscured galaxies (DOGs), we performed X-ray spectral study of 34 DOGs (0.59 ≤ z ≤ 4.65) lying within 5.3 square degrees of the XMM-Spitzer Extragalactic Representative Volume Survey (XMM-SERVS) coverage in the XMM-Large Scale Structure (XMM-LSS) field. To improve the spectral quality of individual sources, we combined all the existing XMM−Newton data and also included Chandra/Advanced CCD Imaging Spectrometer (ACIS) data, whenever available. We find that the X-ray spectra of our DOGs can be fitted with a simple absorbed power law or with a physically motivated borus02 model. The line-of-sight column densities (NH) in our sources span across a wide range (1.02 × 1022 cm−2 ≤ NH ≤ 1.21 × 1024 cm−2), with a substantial fraction (∼17.6 per cent) of them being heavily obscured (NH ≥ 1023 cm−2). We also identified one new Compton-thick (CT)-AGN candidate, yielding the CT-AGN fraction in our sample to be only 3 per cent. The absorption-corrected 2.0–10 keV X-ray luminosities of our sources (2.00 × 1043 erg s−1 ≤ $L_{\rm 2-10~keV}^{\rm int}$ ≤ 6.17 × 1045 erg s−1) suggest them to be luminous quasars. The NH versus Eddington ratio diagnostic plot infers that our sample consists of a heterogeneous population that includes a small fraction (∼12 per cent) of DOGs belonging to an early phase (Hot DOGs) during which accretion and obscuration peaks, while the remaining DOGs belong to an intermediate or late phase during which radiative feedback from the dominant AGN blows away surrounding obscuring material.

Magnetoresistance and magnetic field-induced phase transition in two-dimensional antiferromagnet Fe1/3NbS2

We perform systematic studies on the magnetic and magnetotransport properties of Fe1/3NbS2 single crystal. Results show that Fe1/3NbS2 is an antiferromagnet with strong perpendicular magnetocrystalline anisotropy even in the paramagnetic state. The Fe1/3NbS2 nanoplate exhibits exotic magnetotransport characteristics with variation of temperature and magnetic field in the vicinity of Néel temperature. The temperature dependence of resistivity indicates that the magnetic field has a substantial effect on the Néel order of Fe1/3NbS2, and an intermediate phase occurs before the sample enters into the antiferromagnetic state. It is the field- or temperature-induced antiferromagnetic–intermediate phase and intermediate phase–paramagnetic phase transitions that lead to the novel magnetotransport characteristics in the vicinity of Néel temperature. The findings in this work will promote future studies based on two-dimensional antiferromagnetic spintronics.

Electronic topology with bound defect charges promotes intermediate hexatic phase in two-dimensional melting

Electronic topology with bound defect charges promotes intermediate hexatic phase in two-dimensional melting

The influence of Gaussian pinning on the melting scenario of a two-dimensional soft-disk system: First-order versus continuous transition

Two-dimensional systems are realized experimentally as thin layers on a substrate. The substrate can have some imperfections (defects of the crystalline structure, chemical impurities, etc.) with strong interactions with particles within and near the defects. Such randomly distributed centers of strong interactions are called ”pinning centers”. The presence of random pinning can substantially change the behavior of the system. It not only shifts the melting point of the system, but can also change the melting scenario itself. In the present paper the influence of Gaussian pinning on the melting scenario of a two-dimensional system of soft disks is studied by means of molecular dynamics simulation. We randomly introduce into the system of soft disks a set of “pinning centers” which attract the particles via the Gauss potential. We observe that increasing the depth of a Gaussian well leads to a change in the melting scenario of the system: from melting occurring via a first-order liquid-hexatic transition followed by a continuous hexatic-crystal transition to two continuous transitions through an intermediate hexatic phase. We show that there are still two transition stages for strong disorder, but the melting scenario is qualitatively different from that for weak disorder. The results demonstrate that the simple kind of quenched disorder can significantly affect the melting scenario of two-dimensional systems and offer the possibility of their application for the interpretation of complex experiments.

Progress and landscape of disaster science: Insights from computational analyses

This study identifies trends in disaster science research as well as knowledge gaps at a broad scale in order to help underpin and inform future research in the area. A numerical analysis of 58,106 peer-reviewed articles over four decades reveals key research themes and clusters, their temporal variation of activity as well as the influential studies that have played a key role in their development. Results indicate that what we recognize as contemporary disaster science has only shown discernible patterns of activity and knowledge foundation formation since the 1990s. Disaster research currently constitutes approximately 0.23% of all academic papers published per year. The initial and intermediate phases of the development of the field have been unsystematic and fragmented, with the focus of the field fluctuating for almost two decades until recently when research clusters have shown signs of stabilizing. It is observable that, over the last few years, more attention has been allocated to mitigation, response and recovery by focusing on issues such as the psychological impacts of disasters, reducing exposure to disasters and building community resilience to cope and recover from disasters. This is in contrast with earlier years where the focus was predominantly on preparedness and prevention. Research in different countries has been highly correlated with the types of disasters that occur in their regions, highlighting the relevance of the local situatedness and context in disaster research. The recent emergence and explosive growth of a research cluster linked to flood detection, flood mapping and flood hazard assessment is particularly notable, marking the sharpest growth of a single research cluster ever recorded in this field. A similar trend, though of a smaller magnitude, is observable in relation to research on wildfire hazard. Overall, flood-related research has proven one of the dominant themes, with multiple clusters detectable on the topic, each with their own distinguishable knowledge foundation (i.e., set of references). The pattern of collaboration among disaster researchers is shifting from predominantly domestic research towards international collaborations (currently reaching about 1/3 of all disaster-related papers each year), a sign of recognition to the value of cross-cultural and interdisciplinary perspectives in disaster research.

Exploring Layered Disorder in Lithium-Ion-Conducting Li3Y1-xInxCl6.

Li3Y1-xInxCl6 undergoes a phase transition from trigonal to monoclinic via an intermediate orthorhombic phase. Although the trigonal yttrium containing the end member phase, Li3YCl6, synthesized by a mechanochemical route, is known to exhibit stacking fault disorder, not much is known about the monoclinic phases of the serial composition Li3Y1-xInxCl6. This work aims to shed light on the influence of the indium substitution on the phase evolution, along with the evolution of stacking fault disorder using X-ray and neutron powder diffraction together with solid-state nuclear magnetic resonance spectroscopy, studying the lithium-ion diffusion. Although Li3Y1-xInxCl6 with x ≤ 0.1 exhibits an ordered trigonal structure like Li3YCl6, a large degree of stacking fault disorder is observed in the monoclinic phases for the x ≥ 0.3 compositions. The stacking fault disorder materializes as a crystallographic intergrowth of faultless domains with staggered layers stacked in a uniform layer stacking, along with faulted domains with randomized staggered layer stacking. This work shows how structurally complex even the "simple" series of solid solutions can be in this class of halide-based lithium-ion conductors, as apparent from difficulties in finding a consistent structural descriptor for the ionic transport.

Study on the impact of hydrogen storage temperature on iron-based thermochemical hydrogen storage technology

Thermochemical hydrogen storage technology based on iron-based materials has received significant attention owing to its low cost, safety features, and high volumetric hydrogen storage density. However, no consensus has been established on the optimal temperature range for hydrogen storage. This study investigated the impact of hydrogen storage temperature on hydrogen consumption capacity, hydrogen release capacity, and hydrogen storage energy consumption. The hydrogen storage temperature was optimized with the objectives of low energy consumption and high hydrogen storage density. The experiments were conducted using thermogravimetric analyzer and gram-scale packed-bed reactor setups, accompanied by thermodynamic and kinetic calculations. The research indicated that at 550 °C, the optimal hydrogen storage temperature, the lowest relative energy demand was 32.30 %, with the hydrogen consumption capacity reaching the theoretical maximum value of 4.8 %, and the hydrogen release capacity reaching 4.04 %. Furthermore, achieving the theoretical maximum value of hydrogen consumption capacity became exceedingly difficult when the hydrogen storage temperature exceeded 570 °C. Microstructural characterization and kinetic calculations revealed that this phenomenon was attributed to the formation of a dense iron layer on the particle surface, which impeded the solid-state diffusion of oxygen atoms. The formation of the intermediate phase wüstite was identified as the cause of the formation of the dense iron layer. Overall, this study provided theoretical support for iron-based thermochemical hydrogen storage processes and offered a perspective into the reaction behavior of the reduction of magnetite with hydrogen.

Chemical Bath Deposition of Planar Nickel Oxide Films for Inverted Perovskite Solar Cells and Mini‐Modules

Chemical bath deposition (CBD) is an economical method for the large‐scale preparation of high‐quality inorganic transport layers. In the field of the n–i–p perovskite solar cells (PSCs), the devices based on n‐type CBD–SnO2/CBD–TiO2 structures demonstrate significant advantages in efficiency and stability. However, using CBD method to deposit high‐quality planar p‐type NiOx is challenging due to the anisotropic growth of nickel‐based intermediate phase. Herein, NH4Cl additive is introduced to modulate the intermediate phase by adjusting the concentration of [Ni(H2O)x(NH3)6−x]2+ cations. As a result, dense and uniform NiOx films are finally obtained after thermal annealing. Simultaneously, the energy level and hole conductivity of NiOx materials are carefully controlled by adjusting the annealing temperature. Benefited from the excellent electronic properties of CBD–NiOx hole‐transport layer, the inverted PSCs based on MAPbI3, (FA0.98MA0.02)0.95Cs0.05Pb(I0.95Br0.05)3 achieve the power conversion efficiency of 19.75% and 23.30%, respectively. Furthermore, the unencapsulated devices maintain over 90% of their initial efficiency after continuous operation for 700 h. Scaling up this novel intermediate phase regulation CBD method yields a mini‐module with an active area of 14 cm2, achieving an efficiency of 19.36%.

Topological ordering during flexible to rigid transitions in disordered networks

This contribution focuses on the structural origin of flexible to rigid transitions and the possible underlying intermediate phase which have been reported to occur in a variety of network glasses such as chalcogenides or modified oxides. Here, using molecular dynamics simulations of densified glass-forming liquids, 2SiO 2 -Na 2 O, which are known to display a numerical reversibility window as a signature of an intermediate phase, we focus on structural functions emphasizing topological ordering using the Bhatia–Thornton formalism. Results not only reveal that densified silicates display topological ordering on lengthscales of about 25 Å, but also display obvious threshold behaviors close to the isostatic condition when the network undergoes a flexible to rigid transition. The mechanical constraint count of the atomic network structure reveals that a typical lengthscale characterizing the decay of topological correlations emerges for stressed rigid systems at ≃3.5 Å, whereas small wavevector oscillations are found to be minimal when the isostatic condition is merely satisfied. An additional analysis building on diffusivity and liquid entropy suggests that the locus of flexible to rigid transitions has also connections with water-like anomalies of densified tetrahedral liquids.

Phase transformation mechanism of nominal Si(001) surface driven by hydrogen thermal annealing

Herein, we report the phase transformation mechanism of the nominal Si(001) surface driven by hydrogen thermal annealing. The surface energies of H-terminated Si(001) surface with different phase structures were calculated by density functional theory. The results show that the surface phase with monoatomic steps can transform into the surface phase with diatomic steps under proper ranges of hydrogen chemical potential. Combining thermodynamic and kinetic factors, the phase transformation can’t occur when annealing temperature lower or higher than 800 °C. In addition, surface phases with different types of diatomic steps are alternately transformed through the intermediate phase with monoatomic steps and the imperfection of the transformation process gradually increases with the extension of annealing time. Finally, different experiments have been carried and the experimental results are in good agreement with the phase transformation mechanism. This study provides complete theoretical mechanism and process parameters for controlling the phase structures of the nominal Si(001) surface through hydrogen thermal annealing.

Phase-shifted counterpropagating atmospheric pressure plasma jets: Characterization and interaction with materials

This study investigates the interaction between two counterpropagating atmospheric pressure plasma jets when their respective streamer ignition times are varied by introducing a phase difference between the AC waveforms used to generate them. When the plasma jets are driven in phase, the streamers form at approximately the same time, resulting in a dark region between the two jets. As the phase difference increases, this dark region shifts toward one of the electrodes. With a sufficiently large phase difference, this region vanishes, giving rise to a uniform plasma channel spanning the distance between the electrodes. High-speed imaging reveals that the interaction between the streamers within the channel reduces the streamer propagation length at intermediate phase differences. At large phase differences, the propagation distance of each streamer is enhanced due to the absence of the opposing streamer. Increasing the phase from 0° to 160° reduced the power consumption of the two jets by about 10%, while there was no significant change in the electron density or the N2 vibrational/rotational temperature. Finally, we show how phase-shifting enhances the interaction with three-dimensional objects located between the opposing jets, enabling the treatment of 3D substrates.

Influence of MACl on the Crystallization Kinetics of Perovskite via a Two-Step Method

The addition of methylammonium chloride (MACl) significantly improves the performance and stability of perovskite fabricated by two-step processes. However, its role in crystallization dynamics has not been thoroughly studied. In this work, a comparison study is carried out using different additions of MACl to investigate the impact of the perovskite crystallization dynamics. In situ grazing incidence wide-angle X-ray scattering (GIWAXS) observations during the annealing process of perovskite revealed that the amount of MACl significantly influences the crystallinity and orientation of the perovskite. Increasing the MACl addition enhances the crystallinity of the perovskite in the wet film‘s intermediate phase and strengthens the out-of-plane orientation of the FAPbI3 perovskite α-phase (001) planes during annealing. Moreover, it was found that both excessive and insufficient amounts of MACl introduce defects into the perovskite, which are detrimental to device performance. In contrast, an optimal ratio of MACl-9 mg leads to the formation of uniform and large-grained FAPbI3 perovskite films, with the longest carrier lifetimes (163.7 ns) compared to MACl-5 mg (68.4 ns) and MACl- 13 mg (120.1 ns). As a result, the fabricated MACl-9 mg-based solar cell achieved the highest efficiency (22.63%), which is higher than those of MACl-5 mg (21.47%) and MACl-13 mg (20.07%).

Mechanochemically Induced Solid-State Transformations of Levofloxacin.

Levofloxacin hemihydrate (LVXh) is a complex fluoroquinolone drug that exists in both hydrated and anhydrous/dehydrated forms. Due to the complexity of such a compound, the primary aim of this study was to investigate the amorphization capabilities and solid-state transformations of LVXh when exposed to mechanical treatment using ball milling. Spray drying was utilized as a comparative method for investigating the capabilities of complete LVX amorphous (LVXam) formation. The solid states of the samples produced were comprehensively characterized by powder X-ray diffraction, thermal analysis, infrared spectroscopy, Rietveld method, and dynamic vapor sorption. The kinetics of the process and the quantification of phases at different time points were conducted by Rietveld refinement. The impact of the different mills, milling conditions, and parameters on the composition of the resulting powders was examined. A kinetic investigation of samples produced using both mills disclosed that it was in fact possible to partially amorphize LVXh upon mechanical treatment. It was discovered that LVXh first transformed to the anhydrous/dehydrated form γ (LVXγ), as an intermediate phase, before converting to LVXam. The mechanism of LVXam formation by ball milling was successfully revealed, and a new method of forming LVXγ and LVXam by mechanical forces was developed. Spray drying from water depicted that complete amorphization of LVXh was possible. The amorphous form of LVX had a glass transition temperature of 80 °C. The comparison of methods highlighted that the formation of LVXam is thus both mechanism- and process-dependent. Dynamic vapor sorption studies of both LVXam samples showed comparable stability properties and crystallized to the most stable hemihydrate form upon analysis. In summary, this work contributed to the detailed understanding of solid-state transformations of essential fluoroquinolones while employing greener and more sustainable manufacturing methods.