Differential Scanning Calorimetry Research Articles

Preparation and Characterization of Durian Husk-Based Biocomposite Films Reinforced With Nanocellulose From Corn Husk and Pineapple Leaf.

This research explores the integration of corn husk nanocellulose (CHNc) and pineapple leaf nanocellulose (PLNc) as reinforcing agents in a carboxymethyl cellulose-based film derived from durian husk (CMCDH). Through a solvent-casting method, composite films were fabricated with varying nanocellulose contents (15, 30, and 45 wt%). Analysis using Fourier transform infrared spectroscopy and x-ray diffraction confirmed the effectiveness of alkaline and bleaching treatments in eliminating noncellulosic components. Transmission electron microscopy image revealed the rod-like morphology of CHNc and PLNc, with dimensions approximately 206.5 × 7.2 nm and 150.7 × 6.5 nm, respectively. The inclusion of nanocellulose decreased the transparency of CMCDH films while enhancing their tensile strength, thermal stability, and water vapor transmission rate. Notably, CMCDH/PLNc(30%) exhibited the highest tensile strength at 5.06 ± 0.83 MPa, representing a remarkable 220% increase compared to CMCDH biofilm. Thermogravimetric analysis and differential scanning calorimeter results indicated that nanocellulose incorporation delayed the film's decomposition temperature by approximately 10°C. Moreover, CMCDH/PLNc(30%) demonstrated the lowest water vapor transmission rate, marking a 20% improvement. However, the film's properties were compromised at the highest nanocellulose content (45 wt%) due to observed fiber aggregation, as revealed by scanning electron microscopy analysis.

Enhancing thermal energy storage properties of blend phase change materials using beeswax.

This study aims to use beeswax, a readily available and cost-effective organic material, as a novel phase change material (PCM) within blends of low-density polyethylene (LDPE) and styrene-b-(ethylene-co-butylene)-b-styrene (SEBS). LDPE and SEBS act as support materials to prevent beeswax leakage. The physicochemical properties of new blended phase change materials (B-PCM) were determined using an X-ray diffractometer and an infrared spectrometer, confirming the absence of a chemical reaction within the materials. A scanning electron microscope was used for microstructural analysis, indicating that the interconnection of the structure allowed better thermal conductivity. Thermal gravimetric analysis revealed enhanced thermal stability for the B-PCM when combined with SEBS, especially within its operating temperature range. Analysis of phase change temperature and latent heat with differential scanning calorimetry showed no major difference in the melting point of the various PCM blends created. During the melting/solidification process, the B-PCMs possess excellent performance as characterized by W70/P30 (112.45J.g-1) > W70/P20/S10 (94.28J.g-1) > W70/P10/S20 (96.21J.g-1) of latent heat storage. Additionally, the blends tend to reduce supercooling compared to pure beeswax. During heating and cooling cycles, the B-PCM exhibited minimal leakage and degradation, especially in blends containing SEBS. In comparison to the rapid temperature drop observed during the cooling process of W70/P30, the temperature decline of W70/P30 was slower and longer, as demonstrated by infrared thermography. The addition of LDPE to the PCM reduced melting time, indicating an improvement in the thermal energy storage reaction time to the demand. According to the obtained findings, increasing the SEBS concentration in the composite increased the thermal stability of the resulting PCM blends significantly. Despite the challenges mentioned earlier, SEBS proved to be an effective encapsulating material for beeswax, whereas LDPE served well as a supporting material. Leak tests were performed to find the ideal mass ratio, and weight loss was analyzed after multiple cycles of cooling and heating at 70°C. The morphology, thermal characteristics, and chemical composition of the beeswax/LDPE/SEBS composite were all examined. Beeswax proves to be a highly effective phase change material for storing thermal energy within LDPE/SEBS blends.

How Does the Powder Mixture of Ibuprofen and Caffeine Attenuate the Solubility of Ibuprofen? Comparative Study for the Xanthine Derivatives to Recognize Their Intermolecular Interactions Using Fourier-Transform Infrared (FTIR) Spectra, Differential Scanning Calorimetry (DSC), and X-ray Powder Diffractometry (XRPD).

Molecular interactions between active pharmaceutical ingredients (APIs) and xanthine (XAT) derivatives were analyzed using singular value decomposition (SVD). XAT derivatives were mixed with equimolar amounts of ibuprofen (IBP) and diclofenac (DCF), and their dissolution behaviors were measured using high-performance liquid chromatography. The solubility of IBP decreased in mixtures with caffeine (CFN) and theophylline (TPH), whereas that of DCF increased in mixtures with CFN and TPH. No significant differences were observed between the mixtures of theobromine (TBR) or XAT with IBP and DCF. Mixtures with various molar ratios were analyzed using differential scanning calorimetry, X-ray powder diffraction, and Fourier-transform infrared spectroscopy to further explore these interactions. The results were subjected to SVD. This analysis provides valuable insights into the differences in interaction strength and predicted interaction sites between XAT derivatives and APIs based on the combinations that form mixtures. The results also showed the impact of the XAT derivatives on the dissolution behavior of IBP and DCF. Although IBP and DCF were found to form intermolecular interactions with CFN and TPH, these effects resulted in a reduction of the solubility of IBP and an increase in the solubility of DCF. The current approach has the potential to predict various interactions that may occur in different combinations, thereby contributing to a better understanding of the impact of health supplements on pharmaceuticals.

Azobenzene derivatives with two aliphatic chains: mesogenic and photoisomerisation studies of (E)-4-[(4-heptyloxyphenyl)diazenyl]phenyl alkanoates (7OABOOCm)

ABSTRACT Compounds from the homologous series of (E)-4-[(4-heptyloxyphenyl)diazenyl]phenyl alkanoates (7OABOOCm) for m = 1–19, were synthesised. The phase behaviour was investigated by differential scanning calorimetry, polarised light (optical) microscopy, and thermo-optical analysis. The enantiotropic nematic, smectic C and crystal G phases were found for derivatives with m = 1–18, m = 7–17, and m = 4, respectively. In addition, during cooling, smectic F, crystal G, and unknown X phases were observed for derivatives with m = 7–9, m = 3,8,9, and m = 4, respectively. The X-ray diffraction results suggest that the X phase is presumably monotropic crystal H or a second crystal phase. The E–Z photoisomerisation process was observed during UV light irradiation. A photostationary state was reached after exposure time equal to approximately 80 s. The derived kinetic constant k of this process was of the order of 10−2 s−1.

Double glass transition in polyethylene naphthalate by MDSC, BDS, and TSDC.

In this work, we present an experimental study of the primary and secondary relaxations of the semi-crystalline polymer polyethylene naphthalate by modulated differential scanning calorimetry, Thermally Stimulated Depolarization Currents (TSDCs), and Broadband Dielectric Spectroscopy (BDS) and how they are affected by physical aging. Three dipolar relaxation modes can be observed: from slowest to fastest: the primary α relaxation, which vitrifies at the glass transition temperature, Tgα, and two secondary relaxations, named β* and β. Modulated differential scanning calorimetry results show how the secondary β* relaxation also vitrifies, giving rise to an additional glass transition at Tgβ* < Tgα. In fact, the α and β* relaxations can be considered as part of a very broad and distributed relaxation. Its main part is the primary α relaxation with a shoulder at the high-frequency region corresponding to a complex secondary β* relaxation. BDS results about β* can be modeled by a main contribution (β3*) and two additional ones (β1* and β2*) with a weaker dielectric strength. TSDC results show that each single mode of the relaxation has its own glass transition temperature and they are compatible with the structure inferred by BDS. This scenario gives rise to an extended glass transition dually centered in the Tgβ* ∼ 305K and Tgα ∼ 387K temperatures.

Novel differential scanning calorimetry (DSC) application to select polyhydroxyalkanoate (PHA) producers correlating 3-hydroxyhexanoate (3-HHx) monomer with melting enthalpy.

Polyhydroxyalkanoate (PHA) is an environmental alternative to petroleum-based plastics because of its biodegradability. The polymer properties of PHA have been improved by the incorporation of different monomers. Traditionally, the monomer composition of PHA has been analyzed using gas chromatography (GC) and nuclear magnetic resonance (NMR), providing accurate monomer composition. However, sequential analysis of the thermal properties of PHA using differential scanning calorimetry (DSC) remains necessary, providing crucial insights into its thermal characteristics. To shorten the monomer composition and thermal property analysis, we directly applied DSC to the analysis of the obtained PHA film and observed a high correlation (r2 = 0.98) between melting enthalpy and the 3-hydroxyhexanoate (3-HHx) mole fraction in the polymer. A higher 3-HHx fraction resulted in a lower melting enthalpy as 3-HHx provided the polymer with higher flexibility. Based on this, we selected the poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (P(3HB-co-3HHx)) producing strain from Cupriavidus strains that newly screened and transformed with vectors containing P(3HB-co-3HHx) biosynthetic genes, achieving an average error rate below 1.8% between GC and DSC results. Cupriavidus sp. BK2 showed a high 3-HHx mole fraction, up to 10.38mol%, with Tm(℃) = 171.5 and ΔH of Tm (J/g) = 48.0, simultaneously detected via DSC. This study is an example of the expansion of DSC for PHA analysis from polymer science to microbial engineering.

Synthesis of Quarternized Chitosans and Their Potential Applications in the Solubility Enhancement of Indomethacin by Solid Dispersion.

This study was designed to synthesize quarternized chitosans (Q-CS) and explore their potential application in aqueous solubility enhancement of indomethacin (IND), a BCS class-II drug.Three different Q-CS; N,N,N-trimethyl chitosan chloride (TMC), N-(4-N'-methylpyridinylmethyl) chitosan chloride (mPyCS), and N-(4-N',N',N'-trimethylaminobenzyl) chitosan chloride (TmBzCS) were synthesized and characterized through various spectroscopic analysis. Q-CS-based solid-dispersion (SD) composites of IND (Q-CS-IND) were prepared using the spray-drying methodand characterized through Fourier transform infrared (FTIR), scanning electron microscopy (SEM), differential-scanning calorimetry (DSC), and powder X-ray diffraction (P-XRD). The solubility and dissolution profiles of SD-composites of IND were evaluated and compared with physical mixtures (PM). The IND contents were quantified and validated in the composites using UV-Vis spectrophotometer.FTIR and NMR analysis showed the successful preparation of Q-CS. TMC was found with the highest yield (55.13%) and mPyCS with the highest degree of quaternization (DQ) (63.37%). FT-IR analysisof IND-Q-CS composites demonstrated chemical interaction between carbonyl moieties of IND with functional groups of Q-CS. DSC and PXRD analyses demonstrated the transformation of IND in SD compositesfrom crystalline to an amorphous form. All the IND-Q-CS composites were observed with a significant increase in the solubility and dissolution rate of the drug (1996.0µg/min) compared to PM (1306.8µg/min), which is higher than pure IND (791.6µg/min). The contents of IND in TMC, mPyCS, and TmBzCS composites were 97.69-99.92%, 97.66-100.25%, and 97.18-100.11% respectively.Overall, the findings encourage the applications of Q-CS derivatives for increasing IND water solubility and warrant further in vivo biological profiling of IND composites.

Curing kinetics and mechanical properties of the epoxy vitrimer based on transesterification and its composite laminates

AbstractThe resin is a fundamental factor in determining the performance and usage conditions of its composites. The epoxy vitrimer, which combines both thermoplastic and thermosetting properties, shows significant potential in extending the service life of material. The curing process significantly affects the macroscopic properties of the vitrimer and the resulting carbon fiber reinforced plastics (CFRP). Effective control of curing parameters constitutes the critical factor for the assurance of product quality. In the study, a differential scanning calorimetry (DSC) was utilized to establish a curing kinetics model for a modified, self‐healable epoxy vitrimer based on transesterification. Then the molecular structure, thermodynamic, and mechanical properties of the cured vitrimer were analyzed. Next vitrimeric CFRP (vCFRP) laminates were fabricated, and the tensile and bending properties of the vCFRP laminates were investigated. The results showed the curing process was obtained: 95°C/1 h + 150°C/2 h + 170°C/2 h. The thermodynamic and mechanical properties of cured vitrimer could meet practical requirements. The minimal differences observed in the stress–strain curves of the specimens indicated that the curing process was appropriately configured. The prepared laminates exhibited performance comparable to that of commercial thermosetting composites.

Process optimization in the pyroconversion of native sweet potato starch: structural and functional characterization of pyrodextrin

This work aims to produce dextrin from sweet potato (Ipomoea batatas) starch by pyroconversion. The effect of dextrinization process (roasting time, temperature, and hydrochloric acid concentration) on properties (structural and functional) of starch have been studied using central composite design of experiment. Reaction conditions included: roasting time (55 and 94 min), temperature (127 and 152 °C), and hydrochloric acid concentration (0.17 and 0.43 M). The temperature (quadratic effect X22) is highly significant on the three measured responses (p < 0.05) (Color Index (CI), Turbidity (Turb), and Saccharification Percentage (SP)). Also, the findings indicated that the two most important parameters influencing the pyroconversion of sweet potato starch in the current study were temperature (X2) and hydrochloric acid concentration (X3). The optimal conditions for dextrin production obtained are 94 min, 127 °C and 0.43 M for roasting time, temperature, and hydrochloric acid concentration respectively having 97% of solubility. The FTIR analysis revealed that OH, C-H, C-O, C–C and C-O–H were the main functional groups. These functional groups remained unaffected by the pyroconversion, since the bands extend and the spectrums of all native and pyrodextrin were similar. X-Ray Diffractometry analysis results of dextrin showed that the thermal treatment reduces the crystallinity of starch. Also, this analysis shows starch has CA-type XRD patterns. Scanning Electron Microscopy (SEM) analysis results showed that the defined optimal production maintains the morphology of starch. Differential scanning calorimetry (DSC) used for thermal analysis helps to obtain the glass transition temperature of modified starch equals to 139 °C. Optimal conditions of production of pyrodextrins from sweet potato granule starches could be easily produced with improved physicochemical properties to be used as encapsulating agent or additives in food and chemical industries.

Repercussion of fiber content on the mechanical, thermal, and thermomechanical properties of natural fibers reinforced thermoplastic composites for automotive application

Natural fibers are becoming very popular as a reinforcement in composite materials owing to their benefits, such as low-price, lightweight, availability, and environmental friendliness. In this study, abaca fiber-reinforced polypropylene (PP) and high-density polyethylene (HDPE) composites were created with the help of the injection molding method. Prior to composite fabrication, abaca fibers were chemically treated with a 5 wt% caustic soda (NaOH) solution to improve the bonding between the abaca fibers and the matrix and to enhance their properties. Scanning electron microscopy (SEM) was utilized to assess the fiber surface microstructures before as well as after the chemical treatment, along with the fractured surfaces of tensile specimens. The mechanical properties, such as tensile, bending, and impact strength, of abaca/PP and abaca/HDPE composites were evaluated and compared. Differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) methods were utilized to investigate the thermal behavior of composites. Also, the dynamic mechanical analysis (DMA) method was utilized to explore the thermomechanical properties of the fabricated composites. The outcomes of the experimental findings showed that abaca/PP composite with 10 and 20 wt% fibers is the best choice of material to be used in the automobile industry.

Investigation of the Thermal and Mechanical Properties of Glass Fiber Reinforced ABS/Epoxy Blended Polymer Composite

This research investigates the formation of polymer blends by blending Epoxy LY556 with Acrylonitrile-Butadiene-Styrene (ABS) at weight percentages ranging from 2 to 10% wt. The thermal properties, morphological characteristics, tensile strength, flexural strength, and interlaminar shear strength (ILSS) characteristics of these composites were examined. The X-ray Diffractometer (XRD) and Fourier Transform Infrared Spectrometer (FTIR) studies confirmed the presence of binary blends. The miscibility of epoxy/ABS blends is shown by the presence of a single melting peak in the Differential Scanning Calorimetry (DSC) analysis. The Thermogravimetric Analysis (TGA) findings indicate that epoxy and ABS blends exhibit greater thermal stability than pure epoxy. The tensile strength increased from 183.6 to 380.6 MPa, flexural strength increased from 165.3 MPa to 335.6 MPa, ILSS increased from 32.4 MPa to 72 MPa for 8% wt. of ABS blending, and the laminates witnessed a decrease in density and hardness values. The Scanning Electron Microscopy (SEM) images demonstrate the commendable blending characteristics and the synergistic impact of the ABS/Epoxy composite, yielding superior outcomes to the pure epoxy material.

Release of natural extracts from PVA and PVA-CMC hydrogel wound dressings: a power law swelling/delivery

IntroductionPVA hydrogels present many characteristics of the ideal dressing, although without antimicrobial properties. The present work aims to study the physical, mechanical and release characteristics of hydrogel wound dressings loaded with either of two natural herbal products, sage extract and dragon's blood.MethodsFourier Transform Infrared Spectroscopy (FTIR), Differential Scanning Calorimetry (DSC) and tensile mechanical testing were used to investigate the structure and properties of the gels. Swelling and degradation tests were conducted according to ISO 10993-9. Release characteristics were studied using UV Spectrophotometry.ResultsPVA matrices incorporating sage extract or dragon's blood (DB) present hydrogen bonding between these components. PVA-CMC hydrogels containing sage present similar spectra to PVA-CMC alone, probably indicating low miscibility or interaction between the matrix and sage. The opposite is found for DB, which exhibits more pronounced interference with crystallinity than sage. DB and NaCMC negatively affect Young's modulus and failure strength. All samples appear to reach equilibrium swelling degree (ESD) in 24 h. The addition of DB and sage to PVA increases the gels' swelling capacity, indicating that the substances likely separate PVA chains. The inclusion of CMC contributes to high media uptake. The kinetics profile of media uptake for 4 days is described by a power-law model, which is correlated to the drug delivery mechanism.DiscussionA PVA-CMC gel incorporating 15% DB, the highest amount tested, shows the most favorable characteristics for flavonoid delivery, as well as flexibility and swelling capacity.

Study of thermally induced interactions between active substances from the sartans class and various excipients

AbstractSartans, also known as angiotensin receptor blockers, comprise a category of antihypertensive medications designed to inhibit the actions of angiotensin II (Ang II) in the body, ultimately reducing blood pressure levels. This class of compounds is derived from 2-(1-benzyl-1H-imidazol-5-yl)-acetic acid, with its origin characterized by an imidazole core that underwent various substitutions at specific positions within the heterocyclic nucleus. We investigated the behavior of Losartan, Valsartan and Irbesartan and their compatibility with various excipients used in pharmaceutical tablet formulations by FTIR spectroscopic studies, thermal behavior by thermogravimetry and differential scanning calorimetry. The aim of the study was to determine the excipients to be used in pharmaceutical formulations containing drugs from the class of sartans as active ingredients. Our study concludes by recommending precautionary measures in elaborating new solid formulations containing lactose in the case of Losartan.

A comparative analysis of crustacean exoskeletons: structural, microstructural, morphological, and UV absorption studies

Abstract This study aims to investigate the structural, thermal, and spectral characteristics along with ultra-violet (UV) absorption of various marine benthos exoskeletons, such as various species of crabs (Portunus sanguinolentus, Portunus pelagicus, Charybdis feriata) and mantis shrimp (Oratosquilla oratoria). Their unique properties and ability to survive in harsh oceanic environments make them interesting research subjects. This research utilized powder X-ray diffraction (XRD) analysis to determine the crystal structure of the benthic varieties. The sample surface was analysed using high-resolution micrographs obtained from field-emission scanning electron microscopy (FESEM) identified the presence of chitin and calcite in the marine benthos, which was further confirmed by differential scanning calorimetry (DSC), and Fourier transform infrared spectroscopy (FTIR). The optical characteristics were investigated using UV-visible spectroscopy. The proximate analysis revealed high protein content in the mantis shrimp exoskeleton compared to other crab species, revealing its excellent UV-absorption characteristics. Overall, this research has the potential to broaden our understanding of marine organisms, which can have potential applications in biotechnology and materials science to develop nature-inspired innovative materials sustainably.

Design of Biodegradable PU Textile Coating

Polyurethane (PU) coatings are used in diverse applications such as textile coating. Up to today, landfilling is still the most occurring way of processing PU waste. Biodegradation is an alternative route for processing PU waste and decreases the amount of microplastics in the case of landfilling. In this study, a biodegradable PU textile coating was developed. The PU was characterized via Fourier-transformed infrared (FT-IR) thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). The PU was thermoplastic and had a melting point of approximately 33 °C. The performance of the coating was studied by assessing the water barrier and mechanical properties. The PU coating completely disintegrated, and the biodegradation of PU was assessed in soil and was almost 60%. Furthermore, the plant toxicity was examined by evaluating seedling emergence and growth.

Characterization, processing, and modeling of industrial recycled polyolefins

AbstractThis study aims to establish a systematic approach for characterizing recycled polyolefins of unknown composition, with a specific focus on predicting their performance in film extrusion. We explore various characterization techniques, including differential scanning calorimetry (DSC), Fourier‐transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), and rheometry to assess their effectiveness in identifying the polyethylene (PE) fractions within polypropylene (PP) recyclates. By integrating experimental data with modeling techniques, we aim to provide insights into the predictive capabilities of these techniques in determining processing behaviors. The research highlights the superior fidelity of DSC in predicting the relative fraction and type of PE in a PP recyclate. FTIR is also identified as a high‐fidelity approach, albeit requiring application‐specific calibration. TGA, capillary, and oscillatory rheometry are recognized for their ability to distinguish between grades of recycled polyolefins but provide aggregate behaviors rather than detailed constituent information. 3D flow simulation of the cast film extrusion investigated the effect of the viscosity characterization method, non‐isothermal assumption, and process settings but could not fully replicate the observed variations in the cast film processing of two industrial polyolefins with similar melt flow rates and viscosity behaviors. This underscores the practical challenge of predicting processing issues prior to actual processing, necessitating reliance on reliable instrumentation suites and human expertise for diagnosing and remedying variations.Highlights Two industrial recycled polypropylene materials having similar melt flow rates exhibit drastically different cast film processing behaviors. DSC and FTIR provide reasonable approaches for identifying constituent materials. Modeling of the melt viscosities characterized by capillary and parallel plate rheology suggests that viscosity variations relative to the power‐law behavior assumed in the coat hanger die design is a predominant driver of cast film instabilities.

Novel thermally regenerated flexible cellulose-based films

AbstractIn this work, cellulose powder obtained by acid hydrolysis of industrial Eucalyptus kraft pulp was dissolved in NaOH/Urea/H2O system (7/12/81 wt%) in a concentration of 6% (w/v). Cellulose films were prepared by spreading the dissolved cellulose over glass plates, followed by thermal regeneration – a novel approach reported here for the first time. To obtain final flexible films, plasticization was carried out by immersion in aqueous glycerol solutions of various concentrations (10 to 70 wt%) and hot-pressing (at 0.1 MPa and 105 ºC) was used to dry and compress the cellulose films. The resulting films were characterized by Attenuated Total Reflectance Fourier transform infrared spectroscopy, differential scanning calorimetry, thermogravimetric analysis, X-ray diffraction, contact angle measurements, transparency analysis, and gas permeabilities (oxygen and water vapor). Highly flexible films containing up to 50 wt% of glycerol were successfully obtained, exhibiting no glycerol release upon manual handling. Overall, the produced films demonstrated dense and compact structure, good transparency, flexibility and malleability, and very low oxygen permeability.

Formulation Optimization and Characterization of Solid Lipid Nanoparticles of Apixaban.

Unpredictable situations such as clotting of blood, deep vein thrombosis, and pulmonary embolism arise in the body, which is the leading cause of mortality. Such conditions generally arise after surgery as well as after treatment with oral anticoagulant agents. Apixaban is a novel oral anticoagulant widely recommended for the prevention and treatment of strokes and blood clots suffering from nonvalvular atrial fibrillation by suppressing factor Xa. Apixaban has a log P of 2.71 with poor solubility and reported maximum bioavailability of approximately 50%. Hence, the current research mainly focused on the improvement of solubility, bioavailability, and therapeutic efficacy of Apixaban via solid lipid nanoparticles (SLN). The SLN was developed using the hot-homogenization method using a high-pressure homogenizer. The drug-lipid compatibility study was assessed by the FTIR, and the thermal analysis was performed using differential scanning calorimetry (DSC). During the scrutiny of lipids, the highest solubility of Apixaban was estimated in the glyceryl monostearate, hence selected for the formulation. Moreover, the colloidal solution was stabilized by the polyethylene glycol 200. The Design of Expert software (Version 13, Stat-Ease) was implemented for the optimization analysis by considering the 3-independent factors and 2-dependent parameters. The Patents on the SLN are Indian 202321053691, U.S. Patent, 10,973,798B2, U.S. Patent, U.S. Patent 2021/0069121A1, U.S. Patent 2022/0151945A1. Box-Behnken design was applied along with ANOVA, which showed a p-value less than 0.05 for the dependent parameters such as particle size and entrapment efficiency (p-value: 0.0476 and 0.0379). The optimized batch F10 showed a particle size of 167.1 nm, -19.5 mV zeta potential, and an entrapment efficiency of 87.32%. The optimized batch F10 was lyophilized and analyzed by Scanning electron microscopy (SEM), which showed a particle size of 130 nm. The solid powder was filled into the capsule for oral delivery. The marked improvement in solubility and bioavailability was achieved with F10- loaded Apixaban via Solid lipid nanoparticles. Moreover, the sustained released profile also minimizes the unseen complications that occur due to the clotting of blood.

Misinterpretation of Thermodynamic Parameters Evaluated from Activation Energy and Preexponential Factor Determined in Thermal Analysis Experiments

Thermogravimetry (TGA) and differential scanning calorimetry (DSC) are used broadly to study the kinetics of thermally stimulated processes such as thermal decomposition (pyrolysis) or thermal polymerization. These studies typically yield the activation energy (E) and preexponential factor (A). The resulting experimental values of E and A are oftentimes used to determine the so-called “thermodynamic parameters”, i.e., the enthalpy, entropy, and Gibbs free energy. Attention is called to the persistent and mistaken trend to interpret the resulting quantities as the thermodynamic parameters of the conversion of reactants to products. In fact, these quantities are specific to the conversion of reactants to the activated complex and, as such, provide no insights into the thermodynamics of the conversion of reactants to products. The basics of the activated complex (transition state) theory are provided to explain the meaning of the equations used for evaluating the thermodynamic parameters from the experimental values of E and A. Typical examples of misinterpretation are highlighted and discussed briefly. The applicability of the theory to the systems studied by the thermal analysis kinetics is also discussed.

Development of Eco‐Friendly Chitosan‐Dextran Polyblend Electrolyte for Enhanced Performance in Primary Magnesium Batteries

The potential of next‐generation batteries lies in solid biodegradable polymer electrolytes. This research delves into a solid blend polymer electrolyte (SBPE) for magnesium conduction, utilizing a chitosan‐dextran blend matrix doped with magnesium perchlorate (Mg(ClO4)2) salt. The electrolyte films are prepared using a conventional solution casting technique. Through techniques like X‐ray diffraction and Fourier transform infrared spectroscopy, the successful incorporation of Mg(ClO4)2 into the blend matrix is confirmed. Notably, the SBPE containing 30 wt% of Mg(ClO4)2 demonstrates the highest ionic conductivity of 6.99 × 10−4 S cm−1 and a prominent ionic transference number of 0.84. Thermogravimetric analysis is carried out to study thermal stability. Differential scanning calorimetry analysis of the electrolyte systems gives insight into their thermal properties. Additionally, it showcases favorable electrochemical stability of 2.66 V. The oxidation and reduction peaks are observed in the cyclic voltammetry curve of the highest conducting sample. Furthermore, the discharge performance of Mg/(CS + DN + Mg(ClO4)2)/cathode cells is explored with varied cathode materials, illustrating the SBPE's potential for magnesium‐ion batteries. This study unveils a sustainable, biodegradable, and economical electrolyte solution for advanced energy storage systems.