TGA Analysis Research Articles

The Effect of Residence Time during the Hydrothermal Carbonization Process of Sewage Sludge on the Properties of Hydrochar

The optimal process conditions concerning the hydrothermal carbonization of digested sewage sludge are crucial to the economically effective technology needed to produce a solid product, hydrochar, for energy purposes. Accordingly, different residence times, 0.5 h, 1 h and 2 h, were investigated in order to understand the effect of residence time on the process. Furthermore, the physical and chemical properties of hydrochar were investigated and compared to the raw material. For these reasons, analyses describing fuel properties were performed, including ultimate and proximate analyses, HHV, and TGA analysis. The latter method was employed to study the combustion process of solid samples. In addition, the oxide content of different elements within the ash of solid samples was determined using the XRF method to calculate indices related to operational problems during the combustion process. The results confirmed that time did not matter significantly and the physical and chemical properties of hydrochar were very similar to each other. However, the contact angle for 2 h of residence time confirmed that a longer processing time resulted in a more hydrophobic character of hydrochar and enabled more effective dewaterability of hydrothermal slurry. It was also noted that the hydrothermal carbonization process affected the sewage sludge in a positive way. In brief, the results confirmed that the hydrochar was a brittle, moderately hydrophilic, solid carbon-containing product that provided a different combustion performance than the raw sewage sludge.

Highly Adsorptive Organic Xerogels for Efficient Removal of Metformin from Aqueous Solutions: Experimental and Theoretical Approach

Metformin, widely prescribed to treat type 2 diabetes for its effectiveness and low cost, has raised concerns about its presence in aqueous effluents and its potential environmental and public health impacts. To address this issue, xerogels were synthesized from resorcinol and formaldehyde, with molar ratios ranging from 0.05 to 0.40. These xerogels were thoroughly characterized using FT-IR, SEM, TGA, and TEM analyses. Batch adsorption experiments were performed with standard metformin solutions at concentrations of 50 and 500 mg/L, varying pH, and temperature to determine the adsorption isotherms of the synthesized xerogels. The adsorption data revealed a maximum adsorption capacity of 325 mg/g at pH 11 and 25 °C. Quantum chemical calculations revealed that electrostatic interactions govern metformin adsorption onto xerogels. The xerogels’ adsorption capacity was evaluated in competitive systems with CaCl2, NaCl, MgCl2, and synthetic urines. Reuse cycles demonstrated that xerogels could be reused for up to three cycles without any loss in adsorptive efficiency. The adsorption mechanisms of metformin in the adsorption process highlight the strong electrostatic interactions and hydrogen bonds between the adsorbate and the adsorbent material. Xerogels synthesized show promise as efficient adsorbents to remove metformin from aqueous solutions, helping to mitigate its environmental impact.

Appraising the structural and magnetic properties in template assisted neodymium based metal organic frameworks

This study demonstrates synthesis of two novel lanthanide-based metal-organic frameworks, namely [{NdIII(5 N3-H2isa)2(H2O)2}(H2O)2}]∞ (1) and [{NdIII(5 N3-H2isa)2(H2O)2}(H2O)(1,2-PE)}]∞ (2), synthesized via solvothermal methods using 5-azidoisophthalic acid (5 N3-H2isa) and NdCl3. Both compounds were extensively characterized using single crystal X-ray diffraction, as well as other physicochemical techniques such as IR, TGA, PXRD, and elemental analysis. Structural differences were observed in both compounds depending on the nature of the template molecule used. Compound 1 exhibits an infinite 2D architecture with lattice-occluded water molecules within the 2D layers. In contrast, compound 2, where 1-(-2-pyridyl)-2-(4-pyridyl)ethylene (1,2-PE) was used as the template, shows replacement of interstitial water molecules by the template molecule, resulting in significant changes in overall pore topology which is further corroborated by BET analysis. These structural variations were further supported by magnetic behaviour analyses, indicating an antiferromagnetic behaviour for both compounds.

Cationic Imidazolium-Urethane-Based Poly(Ionic Liquids) Membranes for Enhanced CO2/CH4 Separation: Synthesis, Characterization, and Performance Evaluation.

The escalating emissions of CO2 into the atmosphere require the urgent development of technologies aimed at mitigating environmental impacts. Among these, aqueous amine solutions and polymeric membranes, such as cellulose acetate and polyimide are commercial technologies requiring improvement or substitution to enhance the economic and energetic efficiency of CO2 separation processes. Ionic liquids and poly(ionic liquids) (PILs) are candidates to replace conventional CO2 separation technologies. PILs are a class of materials capable of combining the favorable gas affinity exhibited by ionic liquids (ILs) with the processability inherent in polymeric materials. In this context, the synthesis of the IL GLYMIM[Cl] was performed, followed by ion exchange processes to achieve GLYMIM variants with diverse counter anions (NTf2-, PF6-, and BF4). Subsequently, PIL membranes were fabricated from these tailored ILs and subjected to characterization, employing techniques such as SEC, FTIR, DSC, TGA, DMA, FEG-SEM, and CO2 sorption analysis using the pressure decay method. Furthermore, permeability and ideal selectivity assessments of CO2/CH4 mixture were performed to derive the diffusion and solubility coefficients for both CO2 and CH4. PIL membranes exhibited adequate thermal and mechanical properties. The PIL-BF4 demonstrated CO2 sorption capacities of 33.5 mg CO2/g at 1 bar and 104.8 mg CO2/g at 10 bar. Furthermore, the PIL-BF4 membrane exhibited permeability and ideal (CO2/CH4) selectivity values of 41 barrer and 44, respectively, surpassing those of a commercial cellulose acetate membrane as reported in the existing literature. This study underscores the potential of PIL-based membranes as promising candidates for enhanced CO2 capture technologies.

3D simulation in a fixed bed coupled pervaporation reactor for biodiesel production

In this study, a solid acid catalyst SO42−/TiO2/ZSM-5 (STZ) was prepared. Biodiesel was synthesized from tall oil fatty acid (TOFA) by the ethanol esterification. The fixed bed and pervaporation (PV) coupling increased the esterification conversion of TOFA and ethanol by about 16 %. The spherical STZ catalyst’s appearance, composition, and catalytic activity were assessed through TGA, XRD, SEM, BET, FTIR, NH3-TPD and XPS analyses. The reaction parameters of ethanol/TOFA molar ratio (10:1–20:1), reaction temperature (75–85 ℃), catalyst dosage (6–12 g) and flow rate (0.3–0.9 mL/min) were optimized by the response surface method (RSM). Under RSM optimization, the TOFA esterification reaction achieved a conversion rate of 99.56 ± 0.23 %. After five cycles of esterification, TOFA conversion remained above 87 %. A computational fluid dynamics (CFD) model was established to predict the esterification reaction behavior in the reactor, and the TOFA conversion rate was found to be close to the experimental results through systematic simulation, by reaction kinetics equation, continuity equation, Navier-Stokes equation, and Brinkman equation. In addition, the TOFA biodiesel prepared by this study complies with EN 14214 and ASTM D6751 standards.

Marine waste as a resource: Developing bio-epoxy composites for a sustainable future

Biowastes from discarded fishscales and seashells are rich sources of natural polymers, such as collagen, keratin, and calcium carbonate, that can be used to produce eco-friendly and biodegradable polymer composites. Therefore, utilizing the biowastes for manufacturing polymer composite can offer significant economic, environmental, and social benefits. This experimental study explores the use of Biopoxy matrix (SR33) and fish scale and seashell powders derived from biowastes as filler reinforcements while the composites were manufactured through open mold stir casting technique. Thereafter, the fillers were extracted and processed from raw waste sources, and were characterized using XRD and FTIR analyses. Mechanical and physical properties, including density, water absorption, fracture morphology, flexural, tensile, impact strength, and hardness, were also evaluated to assess the composite's performance. Additionally, thermal properties were investigated through DSC and TGA analyses. Interestingly, the results revealed that green composites with fish scale fillers at 2.5 wt% and seashell fillers at 7.5 wt% exhibited superior performance captured through enhanced mechanical and thermal properties versus control composite samples, suggesting their efficacy in reinforcing the biopoxy matrix. The study underscores the potential of utilizing biowaste-derived fillers for sustainable and eco-friendly composite materials. The combination of biopoxy with these specific filler concentrations presents a promising avenue for developing green composites with favorable mechanical and thermal characteristics, contributing to the ongoing efforts for sustainable material development.

Enhanced curcumin solubility in epichlorohydrin engineered β-Cyclodextrin copolymer for gastric maladies

The present work relates to a β-cyclodextrin based drug delivery system with epichlorohydrin as cross-linking agent, with higher binding efficiency of the drug curcumin and enhanced solubility of the curcumin in complex form when simulated in gastric fluid and increased sustained release of curcumin from complex for 2 h to act in gastric region. Although cross-linking with epichlorohydrin (EPC) is a process studied long time ago, however its use as a gastric solubility enhancer for curcumin has been studied for the first time. The synthesized polymer was well characterized by FT-IR, SEM, XRD, TGA and particle size analysis. The polymer enhanced the water solubility of curcumin by ∼ 800–850 times and the gastric solubility was increased by ∼ 1400–1500 times and acted as a sustained release system as verified by the pepsin inhibition studies which makes it a potential drug carrier for gastric specific drug targeting that can be a promising treatment for gastritis and gastric ulcers.

Modulating dielectric properties of polyimide composite membranes with hydrophobic mesoporous silica via ball milling processing

This research work investigated the impact of the ball-milling (BM) process on the dielectric properties of polyimide (PI) composite membranes incorporating hydrophobic mesoporous silica (HMS) particles. Initially, HMS particles were synthesized through base-catalyzed sol-gel reactions among APTES, MTMS, and TEOS, utilizing D-(−)-Fructose as a template. Following synthesis, the HMS particles underwent ball-milling to fine-tune corresponding specific surface area and average particle size. Three distinctive ball-milled HMS variants (referred to as BMS) were thoroughly characterized using FTIR, 13C NMR, 29Si-NMR spectra, DLS, BET, CA, TGA, SEM, and TEM techniques. Subsequently, a series of PI composite membranes were fabricated and subjected to characterization via FTIR, EDS, CA, and TGA analyses. It should be noted that the three distinctive BM treated HMS was found to exhibit higher specific surface area and hydrophobicity as compared to non-BM treated HMS based on the data of BET and CA, respectively. Moreover, the surface area and hydrophobicity of ball-milled HMS exhibited the upward trend of BMS1 < BMS2 < BMS3. Subsequently, the dielectric constant (Dk) and dielectric loss (Df) of PI and its composite membranes containing HMS particles measured at frequency of 10 GHz was found to show the downward trend. For example, the Dk of PI composite membranes: PI/BMS3 (3.34) < PI/BMS2 (3.41) < PI/BMS1 (3.55) < PI/HMS (3.58) < PI (3.66). On the other hand, the Df of PI composite membranes: PI-BMS3 (0.0113) < PI/BMS2 (0.0114) < PI/BMS1(0.0115) < PI/HMS (0.0121) < PI (0.0123). This resulting decreasing trend of dielectric constant of as-prepared composite membranes may be attributed to the incorporated of HMS particles in PI membrane exhibiting lower moisture absorption (Dk of water = 80) and higher surface area (Dk of air = 1) based on the TGA and CA, respectively.

Synthesis and characterization of sustainable polyurethane-amide (PUA)-organoclay bio-nanocomposites for enhanced protective coatings

An effort has been made to synthesize sustainable polyurethane-amide (PUA) organoclay by incorporating natural materials. Polyol derived from castor oil, toluene diisocyanate (TDI), and cetyl pyridinium chloride (CPC) modified Montmorillonite (Mt) clay have been used in this purpose. The modification of Mt clay with CPC serves a dual purpose by increasing the D-spacing between clay layers and enhancing the compatibility of clay with organic polymers. The investigations included varying the percentage of TDI at three different levels to assess its impact on the physical, mechanical and corrosion resistance characteristics of bio-nanocomposite. The presence of characteristics CH bonds at 2854 cm−1 (sym. −CH2) and 2928 cm−1 (asym. −CH2–) in CMC are absent in Mt, confirming formation of CPC modified Mt clay (CMC). Structural investigations of nanobiocomposites were done by Scanning electron microscopy and X-ray diffraction studies and TGA analysis. The findings suggest that the synthesized bio-nanocomposites could serve as a novel and environmentally friendly material for protective coatings.

Impregnation of Silica Gel with Choline Chloride-MEA as an eco-friendly adsorbent for CO2 capture

Deep eutectic solvents (DES) are a generation of ionic liquids that benefit from low cost, good stability, and environmental-friendly features. In this research, a porous silica gel was impregnated with a eutectic Choline Chloride-Monoethanolamine solvent (ChCl-MEA) to greatly improve its CO2 capture performance. In the impregnation, the weight percentages of ChCl-MEA were used in the range of 10–60 wt% at a temperature of 25 °C. The effect of ChCl-MEA loading on the structural properties of the DES-modified silica samples was studied by BET, FTIR, and TGA analyses. Investigation of the CO2 adsorption performance at different operational conditions showed that the modified silica gel with 50 wt% ChCl-MEA (Silica-CM50) presents the highest CO2 capture capacity of 89.32 mg/g. In the kinetic modeling, the fractional order model with a correlation coefficient of 0.998 resulted in the best fit with the experimental data. In addition, the isotherm data for Silica-CM50 were well-fitted with the Dual site Langmuir isotherm model with a correlation coefficient of 0.999, representing two distinct sites for the adsorption process. Moreover, the thermodynamic parameters including Enthalpy, Entropy, and Gibbs free energy at 25 °C were obtained to be − 2.770, − 0.005 and − 1.162, respectively. The results showed the exothermic, spontaneous and feasibility of the adsorption process.

Enhanced Antibacterial Activity of Vancomycin Loaded on Functionalized Polyketones.

Today, polymeric drug delivery systems (DDS) appear as an interesting solution against bacterial resistance, having great advantages such as low toxicity, biocompatibility, and biodegradability. In this work, two polyketones (PK) have been post-functionalized with sodium taurinate (PKT) or potassium sulfanilate (PKSK) and employed as carriers for Vancomycin against bacterial infections. Modified PKs were easily prepared by the Paal-Knorr reaction and loaded with Vancomycin at a variable pH. All polymers were characterized by FT-IR, DSC, TGA, SEM, and elemental analysis. Antimicrobial activity was tested against Gram-positive Staphylococcus aureus ATCC 25923 and correlated to the different pHs used for its loading (between 2.3 and 8.8). In particular, the minimum inhibitory concentrations achieved with PKT and PKSK loaded with Vancomycin were similar, at 0.23 μg/mL and 0.24 μg/mL, respectively, i.e., six times lower than that with Vancomycin alone. The use of post-functionalized aliphatic polyketones has thus been demonstrated to be a promising way to obtain very efficient polymeric DDS.

Synthesis and Characterization of Thiolated Nanoparticles Based on Poly (Acrylic Acid) and Algal Cell Wall Biopolymers for the Delivery of the Receptor Binding Domain from SARS-CoV-2.

The COVID-19 pandemic required great efforts to develop efficient vaccines in a short period of time. However, innovative vaccines against SARS-CoV-2 virus are needed to achieve broad immune protection against variants of concern. Polymeric-based particles can lead to innovative vaccines, serving as stable, safe and immunostimulatory antigen delivery systems. In this work, polymeric-based particles called thiolated PAA/Schizo were developed. Poly (acrylic acid) (PAA) was thiolated with cysteine ethyl ester and crosslinked with a Schizochytrium sp. cell wall fraction under an inverse emulsion approach. Particles showed a hydrodynamic diameter of 313 ± 38 nm and negative Zeta potential. FT-IR spectra indicated the presence of coconut oil in thiolated PAA/Schizo particles, which, along with the microalgae, could contribute to their biocompatibility and bioactive properties. TGA analysis suggested strong interactions between the thiolated PAA/Schizo components. In vitro assessment revealed that thiolated particles have a higher mucoadhesiveness when compared with non-thiolated particles. Cell-based assays revealed that thiolated particles are not cytotoxic and, importantly, increase TNF-α secretion in murine dendritic cells. Moreover, immunization assays revealed that thiolated PAA/Schizo particles induced a humoral response with a more balanced IgG2a/IgG1 ratio. Therefore, thiolated PAA/Schizo particles are deemed a promising delivery system whose evaluation in vaccine prototypes is guaranteed.

Process integration and techno-economic assessment of crystallization techniques for Na2SO4 and NaCl recovery from saline effluents

Saline effluents containing primarily sodium chloride (NaCl) and sodium sulfate (Na2SO4) are generated from common salt production, tannery CETPs, textiles industries, desalination rejects, etc. In this work, experimental studies have been conducted for parametric evaluation of crystallization techniques for selective isolation of Na2SO4 and NaCl from saline effluent. Three crystallization approaches, i.e., evaporation-crystallization, cooling-crystallization, and antisolvent-crystallization, are assessed through parametric studies. A representative saline solution generated from a salt refinery unit is considered for the study. Lab-scale experiments were performed to determine the optimum process conditions for each crystallization process, and their performance was evaluated by estimating the separation efficiency. Chemical, P-XRD, and TGA analyses were performed to characterize the product composition, purity, and hydration state. For selective Na2SO4 recovery, cooling crystallization, and antisolvent crystallization were found suitable over evaporation crystallization. Subsequently, integrated process variants for cooling crystallization and antisolvent crystallization-based separation were developed. A techno-economic assessment (TEA) was performed to compare integrated process variants for the recovery of salts (Na2SO4 and NaCl) and establish the prospective towards commercialization. The parametric evaluation and TEA shows that the combined crystallization technologies can be potential approach to recover added-value products from saline effluents promoting waste to wealth notion.

Bio-inspired magnetic chitosan/Iron oxide macromolecules for multiple anionic dyes adsorption from aqueous media

Organic anionic dyes are major water pollutants due to their low degradability caused by complex aromatic structures. Not only do they exert toxic, mutagenic, teratogenic, tumorigenic, and genotoxic effects, but they also decrease fertility and cause irritation to the skin and respiratory system in humans. This long-term toxicity has detrimental effects on aquatic organisms and their surroundings, resulting in an imbalanced ecosystem. In this study, a Cs@Fe3O4 magnetic biosorbent was synthesised to uptake three anionic dyes and characterised for FTIR, BET/BJH, XRD, TGA, VSM, and FESEM analyses. The biosorbent average surface area was confirmed to be 52.6524 m2/g, with average pore sizes of 7.3606 nm and 6.9823 nm for adsorption-desorption processes, respectively. Batch adsorption studies pH values, contact times, temperature, initial dye concentrations, and adsorbent dosages were examined. Several isotherm and kinetic models were studied to determine the adsorption mechanism. The adsorption data of these dyes at equilibrium was observed to match Langmuir's isotherm and pseudo-second-order kinetic models. The thermodynamic study revealed that the adsorption process for these dyes was an exothermic reaction. Maximum adsorption capacities for congo red, methyl orange, and metanil yellow were 117.77 mg/g, 137.77 mg/g, and 155.57 mg/g, respectively. The reusability of recovered Cs@Fe3O4 after dye adsorption was evaluated up to five continuous adsorption-desorption cycles for its possible industrial applications.

Enhancing visible light photocatalytic activity of holmium doped g-C3N4 and DFT theoretical insights

In the search of novel photocatalysts to increase the effect of visible light in photocatalysis, g-C3N4 (CN) has become a shining star. Rare earth metals have been used as dopant material to reinforce the photocatalytic activity of CN due to their unique electron configuration recently. In this present study, the pure and different amounts of Ho-doped g-C3N4 (HoCN) photocatalysts were successfully synthesized using urea as a precursor by the one-pot method. Morphological, structural, optical, and vibrational properties of the synthesized photocatalysts were characterized by SEM, EDX, XRD, TGA, XPS, FTIR, PL, TRPL, Raman, DRS, and BET analyses. In addition, theoretical calculations using density functional theory (DFT) were meticulously carried out to delve the changes in the structural and electronic structure of CN with holmium doping. According to calculations, the chemical potential, electrophilicity, and chemical softness are higher for HoCN, while HOMO–LUMO gap, dipole moment, and the chemical hardness are lower for the pure one. Thus, holmium doping becomes desirable with low chemical hardness which indicates more effectivity and smaller HOMO–LUMO gap designate high chemical reactivity. To determine the photocatalytic efficiency of the pure and doped CN photocatalysts, the degradation of methylene blue (MB) was monitored under visible light. The results indicate that holmium doping has improved the photocatalytic activities of CN samples. Most strikingly, this improvement is noticeable for the 0.2 mmol doped CN sample that showed two times better photocatalytic activity than the pure one.

Deciphering the influence of support in the performance of NiFe2O4 catalyst for the production of hydrogen fuel and nanocarbon by methane decomposition

Wet chemical synthesis route was used to synthesis nickel ferrite (NiFe2O4) nanoparticle. Later on the synthesized NiFe2O4 were supported on the surface of three traditional supports such as Al2O3, MgO and TiO2 to get NiFe2O4/Al2O3, NiFe2O4/TiO2 and NiFe2O4/MgO catalysts. The activity profile of each catalyst was evaluated in a fixed-bed reactor for direct methane decomposition at 800 °C. For both fresh and spent catalysts, many characterization techniques have been employed mainly XRD, FESEM, HRTEM, Raman spectroscopy, TGA, and nitrogen adsorption-desorption isotherm. X-ray powder diffraction studies revealed that all synthesized catalysts have a cubic spinel crystal structure. The XRD confirm the presence of NiFe2O4 particles in the component of fresh NiFe2O4/MgO, NiFe2O4/TiO2 and NiFe2O4/Al2O3 catalysts. Temperature Program Reduction (TPR) unveiled the presence of Ni oxides and Fe oxides by displaying reduction peaks in their respective temperature regions. The N2 adsorption-desorption isotherms of the fresh all catalysts reveal that these catalysts have a mesoporous structure. Activity data concluded NiFe2O4/MgO to be the most active catalysts among the tested catalysts methane conversion magnitude of 41.13 % and H2 formation rate of 84.40 × 10−5 mol H2 g−1 min−1. On the other hand, the H2 formation rate drastically declined and very poor activity of both NiFe2O4/TiO2 and NiFe2O4/Al2O3 catalysts was observed in the current work. XRD patterns, FESEM images and TGA analysis of spent NiFe2O4/MgO catalyst shown the filamentous carbon formation which secondarily confirm its higher activity, while its absence in catalysts of NiFe2O4/TiO2 and NiFe2O4/Al2O3. TGA analysis of the carbon deposited on the NiFe2O4/MgO catalyst showed that the amount of carbon was approximately 64 wt%. It was suggested that the formation of nickel-iron carbide revealed by XRD studies of spent catalysts may be the factor related to their poor activity while discussing the structure-activity relationship. Likewise, the higher degree of dispersion related to NiFe2O4/MgO as displayed by XRD, FESEM and TPR investigations, played a vital role in accelerating the rate of hydrogen formation.

Dehydration of Alcohols to Olefins Catalyzed by ZrAPSO-34 Molecular Sieve

The lower olefins (Ethylene, propylene, and butylene) are considered the key to the polymeric and petrochemical industries. Dehydration of alcohols to produce light olefins (Methanol-to-olefins reaction) over SAPO-34 molecular sieve has attractedintoigh attention. Modified SAPO-34 zeolite catalyst with Zr metal was successfully prepared under microwave irradiation using morpholine as a structure direct agent. The microwave energy power used was 800 w and the crystallization time was 200 min. The catalyst sample was characterized by XRD, SEM, EDX, BET, FTIR, and TGA analysis. XRD analysis exhibited a typical chabazite structure with high crystallinity. The analysis showed macrocrystalline particles with moderate distribution of silica in the framework structure and a low surface area of 77 m2/g. The vibration peaks of the prepared catalyst showed agreement with the SAPO-34 CHA structure. Catalyst performance towards methanol-to-olefins conversion was performed in a trickle bed reactor with temperatures of 350, 400, 450, and 500 oC at a weight hourly space velocity of 7.7 h-1. The results also reveal at a temperature of 400 oC , that the best olefins selectivity was obtained, reaching 70%, with a longer lifetime of 500 min. methanol conversion was almost 100% at all reaction temperatures. In addition, the effect of methanol concentration was investigated and the results showed that increasing of water content plays a role in increasing catalyst lifetime and preventing coke depositions in pores.

Novel Biological-Based Strategy for Synthesis of Green Nanochitosan and Copper-Chitosan Nanocomposites: Promising Antibacterial and Hematological Agents.

Two novel samples of nanoparticles based on chitosan were greenly synthesized using pomegranate peel extract. The extract served as a nanoparticle precursor, facilitating the precipitation of nanosized chitosan through the ionic gelation method. Additionally, by mixing the green chitosan nanoparticles with copper ions, a nanoscale composite of chitosan and copper oxide was also produced. Structural and morphological investigations (FTIR, XRD, SEM, EDX, and TGA analyses) were performed for greenly synthesized chitosan nanoparticles and their copper oxide composite to determine all the significant characteristics of those nanoparticles. In addition, both samples were tested using some biological investigations, such as antimicrobial activity and hematological effects. The antimicrobial tests yielded promising results for both the green chitosan nanoparticles and the CuO composite when tested using two bacterial strains and two fungal strains. Moreover, the results showed that using a similar concentration of both green-based chitosan samples resulted in a slightly larger inhibition zone and a lower minimum inhibition concentration (MIC) for the copper oxide chitosan composite compared to the chitosan nanoparticles for all microorganisms included in the test. The mean count of blood components (RBCs and platelets), clotting time, and cholesterol levels in three different blood samples were used to indicate the hematological activity of both greenly synthesized nanoparticles. The results verified a slight reduction in blood component count after the addition of green chitosan nanoparticles, but the chitosan copper oxide composite did not have a noticeable effect on the three blood samples. The chitosan nanoparticles were able to cause a considerable reduction in clotting time and cholesterol levels for all blood samples, thus acting as procoagulants. However, the mixing of CuO with chitosan nanoparticles prolonged the rate of clotting in blood samples from hypercholesteremic individuals, and thus, the mixture acted as an anticoagulant agent.

HEMP FIBER REINFORCED SUSTAINABLE “GREEN” COMPOSITE PRODUCTION WITH EPOXIDIZED SOYBEAN OIL

Due to the rising environmental concerns, industry branches are pushed to research and invest sustainable materials and technologies. In this context, this study aimed to combine a sustainable fiber and matrix material to produce green composite. For this purpose, epoxidized soybean oil and hemp fiber were utilized for composite production. Sebacic acid and maleic anhydride were used as hardeners. Histidine and glycerol were applied as accelerator and starter, respectively. Mechanical performance of the composites was evaluated by tensile and impact tests. Hemp fiber reinforcement resulted in improvement on tensile properties, up to 2.6 MPa tensile strength and 11.7 kJ/m2 impact strength. Thermal properties were determined by TGA and DSC analyses. The changes in molecular level after curing was traced with FTIR measurements and surface morphology was monitored with SEM imaging.

Mimosa/quince seed mucilage–co-poly (methacrylate) hydrogels for controlled delivery of capecitabine: Simulation studies, characterization and toxicological evaluation

This research focused on developing pH-regulated intelligent networks using quince and mimosa seed mucilage through aqueous polymerization to sustain Capecitabine release while overcoming issues like short half-life, high dosing frequency, and low bioavailability. The resulting MSM/QSM-co-poly(MAA) hydrogel was evaluated for several parameters, including complex structure formation, stability, pH sensitivity, morphology, and elemental composition.FTIR, DSC, and TGA analyses confirmed the formation of a stable, complex cross-linked network, demonstrating excellent stability at elevated temperatures. SEM analysis revealed the hydrogels' smooth, fine texture with porous surfaces. PXRD and EDX results indicated the amorphous dispersion of Capecitabine within the network.The QMM9 formulation achieved an optimal Capecitabine loading of 87.17 %. The gel content of the developed formulations ranged from 65.21 % to 90.23 %. All formulations exhibited excellent swelling behavior, with ratios between 65.91 % and 91.93 % at alkaline pH. In vitro dissolution studies indicated that up to 98 % of Capecitabine was released after 24 h at pH 7.4, demonstrating the potential for sustained release.Furthermore, toxicological evaluation in healthy rabbits confirmed the system's safety, non-toxicity, and biocompatibility.