Thermal Stability Research Articles

Synergistic effect of stearic acid/bismuth oxychloride/cupric oxide for thermal storage applications: preparation, stability, rheological and thermophysical analysis

Abstract The present study reports the preparation of nanophase change materials (NPCMs) using a two-step method with an optimized ratio of 0.5 wt.% of nanoparticles for thermal storage applications. Bismuth oxychloride (BiOCl), cupric oxide (CuO), and a mixture of BiOCl/CuO (composite) were used as nanoparticles, and stearic acid was used as the PCM. The crystallography, chemical/functional groups and morphologies of the prepared NPCMs have been analysed by XRD, FT-IR and SEM, respectively. Observations revealed that the presence of nanoparticles in NPCMs did not affect crystal formation or chemical disruption of molecular interactions. TGA was used to analyse the thermal stability and rate of deterioration of the NPCMs. The deterioration of the PCM occurs at 243℃ with a weight loss of 1.3% while 0.5 wt.% concentrated BiOCl, CuO, and composite NPCMs exhibit weight losses of 1.8%, 2.3%, and 3.4%, respectively at 257℃, 262℃ and 258℃. In the DSC study, the phase-changing attributes of the NPCMs manifested in the onset temperature range between 53.4°C and 59.8°C. The potential enthalpy of the PCM is 209.1 kJ/kg, whereas those of the 0.5 wt.% concentrated BiOCl, CuO, and composite NPCMs are 204.6, 198.3, and 201.7 kJ/kg, respectively. However, the enhanced thermal conductivities of 0.5 wt.% concentrated BiOCl, CuO, and the composite NPCMs are 0.18, 0.22, and 0.20 W/(m.℃), respectively, which are 5.9%, 29.4% and 17.6% greater than that of PCM. Additionally, the congruent melting rate increased by 31% for 0.5 wt.% CuO concentrated NPCM; therefore, it is a potential candidate than other NPCMs/PCM. Cyclic tests were conducted to assess the reliability of the NPCMs, and compatible results were obtained even after 500 cycles. The findings of this work indicate that all the prepared NPCMs could be a viable option for practical applications, including thermal comfort buildings, solar heating, and electronic cooling.

Catalysts with Trimetallic Sites on Graphene-like C2N for Electrocatalytic Nitrogen Reduction Reaction: A Theoretical Investigation.

Electrocatalytic nitrogen reduction reaction (NRR) is a green and highly efficient way to replace the industrial Haber-Bosch process. Herein, clusters consisting of three transition metal atoms loaded on C2N as NRR electrocatalysts are investigated using density functional theory (DFT). Meanwhile, Ca was introduced as a promoter and the role of Ca in NRR was investigated. It was found that Ca anchored to the catalyst can act as an electron donor and effectively promote the activation of N2 on M3. In both M3@C2N and M3Ca@C2N (M = Fe, Co, Ni), the limiting potential (UL) is less negative than that of the Ru(0001) surface and has the ability to suppress the competitive hydrogen evolution reaction (HER). Among them, Fe3@C2N is suggested to be the most promising candidate for NRR with high thermal stability, strong N2 adsorption ability, low limiting potential, and good NRR selectivity. The concepts of trimetallic sites and alkaline earth metal promoters in this work provide theoretical guidance for the rational design of atomically active sites in electrocatalytic NRR.

The characteristics of high temperature polymer electrolyte membranes for fuel cell based on 2-pyridene based polybenzimidazole blended with poly(vinyl-phosphonic acid)

The present study has focused on exploring new 2-pyridine-bridge-based polybenzimidazole (2-Py-PBIs) based materials for various energy-related uses in proton exchange membrane fuel cells (PEMFC). An electrochemical device, which transforms chemical energy into electrical energy, is known as fuel cell. Using solution polymerization with polyphosphoric acid as a solvent, a series of 2-Py-PBIs were synthesised from the 4,4'-([2,4′-bipyridine]-2′,6′-diyl)bis (benzene-1,2-diamine). 2-Pyridine bridge Polybenzimidazoles are cross-linked with poly (vinylphosphonic acid), which helps us to improve membrane properties like mechanical properties and proton conductivities. FT-IR was used to characterize chemical structure, Ubbelohde viscometer was employed to determine the inherent viscosity. Additionally investigated were the oxidative stability, swelling ratio, ion exchange capability, and water uptake for 2-Py-PBIs. Thermogravimetric analysis is used to evaluate thermal stability. The obtained 2-Py-PBIs membranes were thermally stable and mechanically strong when compared with conventional polybenzimidazole-based membranes. The 2-Py-PBIs:PVPA membranes showed proton conductivity between 0.10 µS/m to 4.65 µS/m.

Graphene/Polyimide Composite Aerogels for Superior Electromagnetic-Wave-Absorbing Materials with High Thermal Stability and Absorption Effectiveness

Graphene/Polyimide Composite Aerogels for Superior Electromagnetic-Wave-Absorbing Materials with High Thermal Stability and Absorption Effectiveness

Promoter Impact on 5Ni/SAPO-5 Catalyst for H2 Production via Methane Partial Oxidation

Compared to steam reforming techniques, partial oxidation of methane (POM) is a promising technology to improve the efficiency of synthesizing syngas, which is a mixture of CO and H2. In this study, partial oxidation of methane (POM) was used to create syngas, a combination of CO and H2, using the SAPO-5-supported Ni catalysts. Using the wetness impregnation process, laboratory-synthesized Ni promoted with Sr, Ce, and Cu was used to modify the SAPO-5 support. The characterization results demonstrated that Ni is appropriate for the POM due to its crystalline structure, improved metal support contact, and increased thermal stability with Sr, Ce, and Cu promoters. During POM at 600 °C, the synthesized 5Ni+1Sr/SAPO-5 catalyst sustained stability for 240 min on stream. While keeping the reactants stoichiometric ratio of (CH4:O2 = 2:1), the addition of Sr promoter and active metal Ni to the SAPO-5 increased the CH4 conversion from 41.13% to 49.11% and improved the H2/CO ratio of 3.33. SAPO-5-supported 5Ni+1Sr catalysts have great potential for industrial catalysis owing to their unique combination of several oxides. This composition not only boosts the catalyst’s activity but also promotes favorable physiochemical properties, resulting in improved production of syngas. Syngas is a valuable intermediate in various industrial processes.

Effect of polymer concentration and cross-linking density on the microstructure and properties of polyimide aerogels

AbstractPolyimide aerogels display excellent mechanical strength, high thermal stability, low thermal conductivity, and outstanding dielectric properties. Typically, the synthesis of polyimide aerogels involves the polycondensation of dianhydride and diamine into poly(amic acid) (PAA) oligomers, which are then cross-linked and chemically imidized into polyimide. The stoichiometry of dianhydride and diamine determines the number of repeat units and length of the PAA oligomers, which in turn determines the cross-linking density. Despite the critical role of polymer concentration and number of repeating units in determining the microstructure and properties of polyimide aerogels, few detailed studies exist on these two parameters. Here, we synthesized and characterized 16 polyimide aerogel formulations from the common monomers biphenyl-3,3′,4,4′-tetracarboxylic dianhydride (BPDA) and 4,4′-oxydianiline (ODA), with different repeat units (n = 5, 15, 30, 45) and total polymer concentrations (4, 7, 10, 13 wt%). An increased polymer concentration accelerated gelation and enhanced the mechanical performance of aerogels, but surprisingly, it also led to higher volumetric shrinkage during aging, solvent exchange, and supercritical drying (SCD). Specific surface areas (SSAs) reached a maximum at intermediate polymer concentrations. A shorter oligomer chain length, i.e., a higher cross-linking density, led to moderately higher SSAs (between 320 and 400 m2/g) and reduced shrinkage, resulting in lower densities for a given polymer concentration. The density dependence of the thermal conductivity exhibits a pronounced U-shaped curve with a minimum in thermal conductivity of 21–23 mW/(m·K) between 0.080 and 0.120 g/cm3, with somewhat lower values for more highly cross-linked aerogels. This systematic study of polyimide aerogels forms the basis for designing polyimide aerogels with tailored properties for targeted applications. Graphical Abstract

Anisotropic materials with abnormal Poisson's ratios and acoustic velocities.

Isotropic materials are required to adhere to various mechanical principles due to their limited thermal stability. For instance, it is essential for Poisson's ratio to be within the range of -1 to 0.5, and the longitudinal wave velocity must exceed the transverse wave velocity. Nevertheless, perfect crystals, as anisotropic materials, have the ability to defy conventional rules. Through the integration of high-throughput processes and first-principles calculations, a comprehensive exploration of known materials was conducted, resulting in the establishment of a database featuring an extreme anisotropic mechanism. This included the identification of abnormal Poisson's ratios (with the directional Poisson's ratio ranging from -3.00 to 3.67), the discovery of extreme negative linear compressibility, the determination of the upper and lower limits of the sound velocity, and other associated properties. Several materials with abnormal Poisson's ratios (<-1 or >0.5) were listed, and their peculiar mechanical behavior, wherein the volume decreased counterintuitively with uniaxial tension, was discussed. Finally, this study focused on the velocities of longitudinal and transverse waves, with specific emphasis on materials exhibiting transverse wave velocities that exceeded the longitudinal wave velocities.

Comparative Study between Multiwall Carbon Nano Tube and Carbon Waste from Aluminium Production in the Preparation of Thermally Stable Cementitious Mortar

Objective: The objective of this study is to conduct a comparative investigation into the performance of multiwall carbon nanotube (MWCNT) and carbon wastes (C-waste) derived from the aluminum industry in the creation of thermally stable cementitious mortar. Specifically, the research aims to assess their impact on compressive strength and thermal stability, with a focus on identifying the superior additive for enhancing the properties of cement mortar. Methods: Cement mortar is produced using a blend of CEMIII cement and sand passing through a 1 mm sieve. Various ratios of MWCNT and C-waste, ranging from 0.1% to 0.7%, are incorporated into the mixture. Compressive strength tests are conducted at different intervals, up to 90 days, to evaluate the effects of additives on strength enhancement. Additionally, the resistance to high temperatures is examined by subjecting the mortar samples to firing temperatures up to 700 degrees Celsius. Results: The inclusion of both MWCNT and C-waste leads to improvements in compressive strength values, with the most significant enhancement observed at 0.1% concentration, resulting in approximately 70MPa and 75MPa at 90 days, respectively. Notably, C-waste demonstrates superior physical and mechanical properties compared to MWCNT, along with a lower production cost. Moreover, both additives exceed the specified limits for thermal resistance in mortar, achieving measurements of about 60MPa for MWCNT and 63MPa for C-waste when exposed to firing temperatures of 700 degrees Celsius. These results highlight the higher thermal stability of C-waste relative to MWCNT. Conclusion: In conclusion, this study confirms the efficacy of utilizing C-waste as an additive in cementitious mortar production, showcasing its superior performance over MWCNT in terms of compressive strength enhancement and thermal stability. The findings underscore the potential of repurposing industrial by-products such as C-waste to improve material properties while also addressing environmental concerns and reducing production costs in construction applications.

Multi‐response optimization of characteristics for graphite reinforced biodegradable PVA‐fumaric acid cross‐linked composite: A gray‐fuzzy logic‐based hybrid approach

AbstractIn the current investigation, enhancement in the mechanical properties, thermal stability, and decrement in the moisture absorption capabilities of polyvinyl alcohol was observed by cross‐linking it with different weight percentages (wt. %) of fumaric acid and reinforcing them along with sulfuric acid‐modified graphite particles. The effects of altering the cross‐linking duration and fumaric acid wt. % were investigated in the resulting composite using the Taguchi L16 experimental design method. As in this contemporary era of rapid industrial expansion and fierce competition, the primary goals of manufacturers revolve around the production of high‐quality goods at optimal costs within a specified timeframe. Therefore, to save both cost and time, the authors have utilized a technique known as “gray‐fuzzy optimization” to balance competing goals between mechanical (toughness, elongation and strength) and physical (water intake capacity) attributes. The present approach aimed to reduce the experimentation expenses and increase the effectiveness of composite manufacturing by considerably reducing the intricacy of practical multi‐response optimization issues. Response graphs and analysis of variance tests were also utilized to calculate the percentage contribution of the input variables and provide model significance.Highlights Polyvinyl alcohol is cross‐linked with different weight percentages (wt. %) of fumaric acid, and reinforced them with sulfuric acid‐modified graphite particles. Enhancement in mechanical properties, thermal stability, and decrease in moisture absorption capabilities were perceived for the fabricated composite. Effects of altering the cross‐linking duration and fumaric acid wt. % were investigated in the resulting composite using the Taguchi L16 experimental design. Gray‐fuzzy optimization technique was utilized to balance competing goals between water intake and mechanical attributes like toughness, elongation and strength. Response graphs and analysis of variance (ANOVA) tests were also utilized to evaluate the percentage contribution of input variables and provide model significance.

Enhancing Carbon Fiber Fabrics with ALD AlxOy Coatings: An Investigation of Thickness Effects on Weight, Morphology, Coloration, and Thermal Properties

This study explores the impact of non-stoichiometric aluminum oxide (AlxOy) coatings applied via thermal atomic layer deposition (ALD) on carbon fiber fabrics (CFFs), emphasizing volume per cycle, FESEM analyses, color transitions, and thermal stability enhancements. Using trimethylaluminum and water at 100 °C, AlxOy was deposited across a range of 1000 to 5000 ALD cycles, with film thicknesses extending up to 500 nm. This notable increase in the volume of material deposited per cycle was observed for the 3D CFFs, highlighting ALD’s capability to coat complex structures effectively. FESEM analyses revealed the morphological evolution of CFF surfaces post-coating, showing a transition from individual grains to a dense, continuous layer as ALD cycles increased. This morphological transformation led to significant color shifts from green to red to blue, attributed to structural coloration effects arising from variations in film thickness and surface morphology. Thermogravimetric analyses (TGA and dTG) indicated that the AlxOy coatings enhanced the thermal stability of CFFs, with a postponement in degradation onset observed in samples subjected to more ALD cycles. In essence, this research highlights the nuanced relationship between ALD processing parameters and their collective influence on both the aesthetic and functional properties of CFFs. This study illustrates ALD’s potential in customizing CFFs for applications requiring specific color and thermal resilience, balancing the discussion between the surface morphological changes and their implications for color and thermal behavior.

Application of modified kaolinite in improving thermal stability of polydimethylsiloxane

AbstractThis research investigated the chemical structure and morphology of the hydrogenated tallow amine (HTA)‐intercalated kaolinite by XRD, FT‐IR, and TEM measurements. The experimental outcomes show that intercalation of kaolinite by HTA, with an intercalation rate of 63.2%, expands the interlayer distance with a subsequent dominant basal XRD peak at 2θ ≈ 7.9°. Furthermore, a composite was created from the HTA‐intercalated kaolinite and polydimethylsiloxane (PDMS) through a favorable interaction between the end silanol groups of PDMS and the modified kaolinite surface. Thermogravimetry‐differential scanning calorimetry results indicate that introducing the HTA‐intercalated kaolinite into the PDMS matrix increases the thermal stability of the composite from 178 to 343 °C. However, the thermal stability of the composite is lower than that of other published materials. The synthesis of kaolinite/PDMS composite with enhanced structural and thermal stability outcomes has been provided via a simple and effective solution method that should have further applications.

Surfactant-Assisted Förster Resonance Energy Transfer from a Quantum Dot Complex for Highly Stable White Light Emission.

Herein we report the fabrication of a surfactant modified quantum dot complex (S-QDC, having λem = 485 nm) nanocomposite (composed of cetyltrimethylammonium bromide surfactants and a zinc-quinolate complex attached ZnS quantum dot), the donor capability of S-QDC in Förster resonance energy transfer (FRET) with an acceptor organic molecule (λem = 573 nm), and finally their utilization in the FRET-based white light emission having features near to mid-day sunlight. The Förster distance, energy transfer efficiency, donor-acceptor distance, number of binding sites, and binding constant are evaluated to be 3.48 nm, 85.74%, 2.58 nm, 0.94, and 1.87 × 104 M-1, respectively, for the current electrostatically driven FRET pair. The solid polymer coated FRET pair composite emits white light having chromaticity color coordinates of (0.33, 0.33) and correlated color temperature of 5350 K and also shows long-term atmospheric white luminescence stability up to 30 days, photostability, and thermal stability with preservation of their pristine morphology.

Advancing soy protein isolate-ulvan film physicochemical properties and antioxidant activities through strategic high-pressure homogenization technique

Soy protein-based films often exhibit poor properties, including limited mechanical strength, stability, and bioactivity, which hinder their extensive application in the food industry, particularly in edible packaging. To enhance the properties of soy protein-based films, we employed high-pressure homogenization (HPH) to modify the soybean protein isolate (SPI) molecules and sought to cross-link SPI with ulvan polysaccharide, which possesses distinctive bioactivities. The results confirmed that soluble ulvan polysaccharides were incorporated into the cross-linking system through hydrogen bonding. Results indicated that HPH treatment enhanced SPI's solubility and surface hydrophobicity (H0), promoting hydrogen bonding and hydrophobic interactions between SPI and ulvan, as evidenced by ζ-potential and turbidity measurements. Structural and microstructural analyses of both individual SPI and composite films, using FT-IR, XRD, CD and SEM, demonstrated a high compatibility between HPH-treated SPI and ulvan. The incorporation of ulvan reduced the films' tensile strength (TS), but higher pressure significantly improved it (p < 0.05). Post-HPH modification, the films exhibited increased contact angle and swelling capacity (p < 0.05), indicating enhanced hydrophobicity. Higher pressure treatments resulted in more opaque and yellowish films, thereby diminishing ultraviolet light transmission. Thermal stability analyses, via TGA-DSC, showed that U-HSPI films had improved thermal stability compared to pure SPI films. Moreover, ulvan inclusion boosted the antioxidant capacity of SPI films, especially after HPH treatment. Overall, this study confirms that HPH modification substantially influences the properties and activities of SPI-based films, and the complex films based on SPI and ulvan with improved physicochemical and antioxidant properties exhibit a great potential in the food packaging field.

Colorless and transparent polyimide nanocomposites using organically modified montmorillonite and mica

In this study, we introduce a method for replacing the glass used in existing display electronic materials, lighting, and solar cells by synthesizing a colorless and transparent polyimide (CPI) film with excellent mechanical properties and thermal stability using a combination of new monomers. Poly(amic acid) (PAA) was synthesized using dianhydride 4,4′-biphthalic anhydride (BPA) and diamine 2,2-bis(3-amino-4-hydroxyphenyl) hexafluoropropane (AHP). Various contents of organically modified montmorillonite (MMT) and mica were dispersed in PAA solution through solution intercalation, and then CPI hybrid films were prepared through multi-step thermal imidization. The organoclays synthesized to prepare CPI hybrid films were Cloisite 93A (CS-MMT) and hexadimethrine-mica (HM-Mica) based on MMT and mica, respectively. In particular, the diamine monomer AHP containing a –OH group was selected to increase the dispersibility and compatibility between the hydrophilic clays and the CPI matrix. To demonstrate the characteristics of CPI, the overall polymer structure was bent and a strong electron withdrawing –CF3 group was used as a substituent. The thermomechanical properties, morphology of clay dispersion, and optical transparency of the CPI hybrid films were investigated and compared according to the type and content of organoclays. Two types of organoclays, CS-MMT and HM-Mica, were dispersed in a CPI matrix at 1 to 7 wt%, respectively. In electron microscopy, most of the clays were uniformly dispersed in a plate-like shape of less than 20 nm at a certain critical content of the two types of organoclays, but agglomeration of the clays was observed when the content was higher than the critical content. Hybrids using HM-Mica had better thermomechanical properties and hybrids containing CS-MMT had better optical transparency.

Recycling of Polydicyclopentadiene Enabled with N-Coordinated Boronic Bonds.

In this contribution, we reported the transformation of polydicyclopentadiene (PDCPD) from thermoset into vitrimer. First, two N-coordinated diboronic diols were successfully synthesized via the reaction of N,N,N-tri(2-hydroxyethyl)amine and/or N,N,N",N"-tetrakis(2-hydroxyethyl)ethylene diamine with 4-(hydroxymethyl) phenylboronic acid and then they were transformed into two N-coordinated cyclic boronic diacrylates. The latter two dienes carrying electron-withdrawing substituents were used for the ring opening insertion metathesis copolymerization (ROIMP) of dicyclopentadiene to afford the crosslinked PDCPD. In the crosslinked PDCPD networks, N-coordinated cyclic boronic bonds were integrated. It was found that the as-obtained PDCPD networks displayed the excellent reprocessing properties. In the meantime, the fracture toughness was significantly improved. Owing to the inclusion of N-coordinated cyclic boronic ester bonds, the modified PDCPDs had the thermal stability much superior to plain PDCPD. The results reported in this work demonstrated that PDCPD can successfully be transformed into the vitrimers via the introduction of N-coordinated cyclic boronic ester bonds. This article is protected by copyright. All rights reserved.

Impact of multi‐walled carbon nanotubes on the thermal, mechanical, and electrical properties of guar gum hydrogel

AbstractThis research investigates the transformative impact of incorporating unmodified multi‐walled carbon nanotubes (um‐MWCNTs) on properties of guar gum (GG)‐based hydrogel. The study focuses on the enhancement of thermal stability, mechanical strength, and electrical properties of hydrogel composite. Thermal analysis reveals a significant increase in residual weight remaining at 430°C from 3% to 10% with the addition of 0.2 wt% um‐MWCNTs to GG hydrogel. Viscoelastic properties of hydrogel composite investigated by rheology analysis observed that enhancements in storage modulus from 0.2 to 2.2 MPa indicative of enhanced structural integrity. Moreover, electrical conductivity exhibits a substantial increase with the addition of nanotubes, indicating the potential applicability of the composite in electronic and sensing applications. This research showcases the potential of GG/um‐MWCNT composites for diverse applications in biomedicine, sensors, and advanced materials.Highlights Distribution of um‐MWCNTs into guar‐gum matrix to obtain maximum benefits. Inclusion of um‐MWCNTs improves the rheological properties of GG/um‐MWCNTs composites. Rheological properties can be tuned with um‐MWCNT content. MWCNTs improved thermal stability of the GG hydrogel. MWCNTs improved electrical conductivity of the GG hydrogel.

Study on the characteristics of glass fiber‐reinforced polymers from recycled wind turbine blades as reinforcement in particleboard

AbstractGlass fiber‐reinforced polymer (GFRP), extensively employed in diverse industries, generates considerable waste, especially from decommissioned wind turbine blades. Our research group has developed a new method of mechanical recovery for GFRP from wind turbine blades. In this study, waste GFRP was processed into a mixed particle size of 0.9–6 mm using a crusher and a screening machine, and then added as reinforcement materials to particleboards. The effects of different levels of four factors (GFRP addition, hot pressing temperature, hot pressing time, and binder dosage) on the properties of GFRP particleboards were evaluated by orthogonal experiments. The study results showed that the particleboards with 30 wt% GFRP improved modulus of rupture (MOR), modulus of elasticity (MOE), and internal bonding strength (IB) by 74.94%, 42.28%, and 92.05%, respectively, compared to pure poplar particleboards. Moreover, GFRP particleboards demonstrated better water resistance and dimensional stability than commercial particleboards and excelled in thermal stability. Recycling GFRP waste from decommissioned wind turbine blades and incorporating it into particleboard production can reduce environmental pollution, increase the resource recovery utilization rate, and contribute to sustainable manufacturing practices.Highlights Low‐cost and efficient methods of recycling wind turbine blades were proposed. Recycled GFRP from wind turbine blades can be used as reinforcement for particleboard. The prepared particleboards have excellent physical and mechanical properties and are thermally stable. Determination of the optimal glass fiber‐reinforced polymer addition level in particleboard at 30 wt%.

Halloysite nanotubes immobilized by copper itaconic acid complexes as smoke suppressant for soft polyvinyl chloride

AbstractCurrently, there are few reports of core–shell‐structured smoke suppressants that can provide a growth substrate and stabilize the char layer. In response to this problem, core–shell nanoparticles of halloysite nanotubes (HNTs) coated with copper itaconate complex were prepared by layer‐by‐layer assembly method. The electrostatic forces between HNTs and copper ions and the coordination between the itaconic acid and copper ions contributed this synthesis. The micromorphology, chemical composition, and structure of HNT@CuC5H4O4 were characterized, and its effects on the flame‐retardant and smoke‐inhibition properties, mechanical properties, and thermal stability of the soft polyvinyl chloride (PVC) were investigated. The results showed that the core–shell structure of HNT@CuC5H4O4 contributed to its homogeneous dispersion in PVC and the formation of interlocking mesh structure. Thus, the incorporation of HNT@CuC5H4O4 enhanced the strength and stiffness of soft PVC without sacrificing its ductility. Besides, copper ions on HNT@CuC5H4O4 could promote the cross‐linking carbonization of the PVC at high temperature. The formed char layer catalyzed by CuC5H4O4, together with its attached three‐dimensional network structure of HNT constituted a compact and continuous char layer with high thermal stability, which effectively prevented the release of combustible volatiles and toxic gases as well as heat transfer.

A Review on cLF36, a Novel Recombinant Antimicrobial Peptide-Derived Camel Lactoferrin.

Lactoferrin is an antimicrobial peptide (AMP) playing a pivotal role in numerous biological processes. The primary antimicrobial efficacy of lactoferrin is associated with its N-terminal end, which contains various peptides, such as lactoferricin and lactoferrampin. In this context, our research team has developed a refined chimeric 42-mer peptide known as cLF36 over the past few years. This peptide encompasses the complete amino acid sequence of camel lactoferrampin and partial amino acid sequence of lactoferricin. The peptide's activity against human, avian, and plant bacterial pathogens has been assessed using different biological platforms, including prokaryotic (P170 and pET) and eukaryotic (HEK293) expression systems. The peptide positively influenced the growth performance and intestinal morphology of chickens challenged with pathogen bacteria. Computational methods and in vitro studies showed the peptide's antiviral effects against hepatitis C virus, influenza virus, and rotavirus. The chimeric peptide exhibited higher activity against certain tumor cell lines compared to normal cells, which may be attributed to the peptide's interaction with negatively charged glycosaminoglycans on the surface of tumor cells. Importantly, this peptide exhibited no toxicity against host cells and demonstrated remarkable thermal and protease stability in serum. In conclusion, while our investigations suggest that the chimeric peptide, cLF36, may offer potential as a candidate or complementary option to some available antibiotics, antiviral agents, and chemical pesticides, significant uncertainties remain regarding its cost-effectiveness, as well as its pharmacodynamic and pharmacokinetic characteristics, which require further elucidation.

Synthesis, structure and photoluminescence properties of heterometallic-based coordination polymers of trimesic acid.

Reacting trimesic acid (H3TMA, C9H6O6) with CaCl2 and MCl2 at 110 °C under hydrothermal conditions gave the isostructural heterobimetallic coordination polymers (CPs) catena-poly[[tetraaquazinc(II)]-μ-5-carboxybenzene-1,3-dicarboxylato-[tetraaquacalcium(II)]-μ-5-carboxybenzene-1,3-dicarboxylato], [CaZn(HTMA)2(H2O)8]n, 1, and catena-poly[[tetraaquacobalt(II)]-μ-5-carboxybenzene-1,3-dicarboxylato-[tetraaquacalcium(II)]-μ-5-carboxybenzene-1,3-dicarboxylato], [CaCo(HTMA)2(H2O)8]n, 2. Compounds 1 and 2 crystallize in the monoclinic space group C2/c. The solid-state structures consist of eight-coordinate CaII ions and six-coordinate MII ions. These ions are connected by a doubly deprotonated HTMA2- ligand to create a one-dimensional (1D) zigzag chain. Poly[[decaaquabis(μ3-benzene-1,3,5-tricarboxylato)calcium(II)dizinc(II)] dihydrate], {[CaZn2(TMA)2(H2O)10]·2H2O}n, 3, was found incidentally as a minor by-product during the synthesis of 1 at a temperature of 140 °C. It forms crystals in the orthorhombic space group Ccce. The structure of 3 consists of a two-dimensional (2D) layer composed of [Zn(TMA)] chains that are interconnected by CaII ions. The presence of aromatic carboxylic acid ligands and water molecules, which can form numerous hydrogen bonds and π-π interactions, increases the stability of the three-dimensional (3D) supramolecular architecture of these CPs. Compounds 1 and 2 exhibit thermal stability up to 420 °C, as indicated by the thermogravimetric analysis (TGA) curves. The powder X-ray diffraction (PXRD) data reveal the formation of unidentified phases in methanol and dimethyl sulfoxide, while 1 exhibits chemical stability in a wide range of solvents. The luminescence properties of 1 dispersed in various low molecular weight organic solvents was also examined. The results demonstrate excellent selectivity, sensitivity and recyclability for detecting acetone molecules in aqueous media. Additionally, a possible sensing mechanism is also outlined.