Thermal Degradation Temperature Research Articles

Semi-Interpenetrating Polymer Network Anion Exchange Membranes Based on Quaternized Polybenzoxazine and Poly(Vinyl Alcohol-Co-Ethylene) for Acid Recovery by Diffusion Dialysis.

Acid recovery from acidic waste is a pressing issue in current times. Chemical methods for recovery are not economically feasible and require significant energy input to save the environment. This study reported a semi-interpenetrating polymer network (semi-IPN) anion exchange membranes (AEMs) for acid recovery by diffusion dialysis with excellent dimensional stability, high oxidation stability, good acid dialysis coefficient (UH +) and high separation factor (S). Semi-IPN AEMs are prepared by ring-open cross-linked quaternized polybenzoxazine (AQBZ) with poly(vinyl alcohol-co-ethylene), where AQBZ is obtained by Mannich reaction and Menshutkin reaction. All four proportions of semi-IPNs exhibit clear micro-phase separation, which is conducive to ion transport. The water uptake (WU) of the four semi-IPNs ranges from 14.2 % to 19.2 %, while the swelling ratio (SR) remains between 8.7 % and 11.3 %. These results indicate that the cross-linked structure in the designed semi-IPNs effectively control swelling and ensure dimensional stability. The thermal degradation temperature (Td5) of semi-IPN4:6 to semi-IPN7:3 varies from 309 °C to 289 °C, with an oxidation stability weight loss rate (WOX) ranging from 91.5 % to 93.5 %, demonstrating excellent thermal stability and oxidation stability. The semi-IPNs also show good UH + values ranging from 11.9-16.3*10-3 m/h and high S values between 38.6 and 45.9, indicating the promising potential of the semi-IPNs.

Ultrasound and enzyme treatments on morphology, structures, and adsorption properties of cassava starch

Porous starch materials are environmentally friendly and renewable and exhibit high adsorption performances. Ultrasound and compound enzyme (α-amylase and glucoamylase) treatments were applied to prepare modified cassava starch. The granules, crystal morphology, crystal structure, and molecular structure of starch were investigated. The hydrolysis degree, solubility, swelling, and adsorption properties of cassava starch were analyzed. After the cassava starch was modified by ultrasound and enzyme treatments, the granule size of the starch decreased, and the surfaces were eroded to form pits, grooves and cavity structure. The starch spherulites weakened or even disappeared. The functional groups of starch did not change significantly, but the degree of crystal order decreased. The double-helix structure was reduced, and the crystal structure was composed of A + V-type crystals, with a decrease in crystallinity. The gelatinization temperature and thermal degradation temperatures enhanced. The enzymatic hydrolysis degree and solubility of the modified cassava starch increased. The swelling degree decreased, and oil adsorption, water adsorption improved. MB adsorption behavior of modified cassava starch closely followed a pseudo-second-order kinetics model and the Langmuir isotherm equation. These findings could help to understand the relationship between the structure and properties of modified starch, and guide its application in the field of adsorption.

Thermal Degradation and Chemical Analysis of Flame-Retardant-Treated Jute Fabrics.

Jute is an inherent lignocellulosic fiber, consisting of hemicellulose, α-cellulose, and lignin. Industrial ventilation, automotive composites, upholstery, carpets, military uniforms, hospital furnishings, and curtains necessitate the integration of flame-retardance properties into jute fibers. In this investigation, seven weave-structured jute fabrics were treated using an organophosphorus-based flame-retardant (FR) chemical (ITOFLAM CPN) and a crosslinking agent (KNITTEX CHN) by the pad-dry-cure method. The thermal stability, degradation and pyrolysis behavior of jute was measured using a thermogravimetric analyzer (TGA). Surface morphology and element distribution were scrutinized utilizing a scanning electron microscope (SEM) and an energy-dispersive spectrometer (EDS). The ATR-FTIR (Attenuated Total Reflection-Fourier Transform Infrared Spectrometer) technique has been employed for analyzing the composition of chemicals in the jute fabrics. According to the protocols specified in ISO 14184-1, free formaldehyde detection was carried out on the jute fabrics. The flame-retardance property was significantly improved on all of the jute fabrics after FR treatment. FTIR and SEM-EDS studies revealed the presence of FR chemical deposition on the surface of the jute fabrics. TGA analysis indicated that the fabrics treated with FR exhibited premature degradation, leading to the generation of more char compared to untreated samples. The jute fabrics specifically demonstrated a notable enhancement in residual mass, exceeding 50% after FR treatment. However, it is noteworthy that the FR-treated fabrics exhibited an elevated level of free formaldehyde content, surpassing the permissible limit of formaldehyde in textiles intended for direct skin contact. The residual mass loss percentage after ten washes of FR-treated fabrics remained in a range from 32% to 36%. Twill weave designed fabrics (FRD4 and FRD5) clearly showed a lower thermal degradation temperature than the other weaves used in this study.

Development of polysaccharide bioplastic: Analysis of thermo-mechanical properties and different environmental implications

Despite the distinct benefits of plastics, the environmental impacts stemming from their production and accumulation in the environment have become a global concern. Therefore, the development of new technologies that mitigate these impacts is of notable importance. The present study aimed to evaluate the physicochemical properties of starch-xylan-based bioplastic, and to discuss the viability of this material in terms of applications and ecological impacts. Holocellulose, xylan, and α-cellulose were extracted from waste biomass and combined with starch for bioplastic production. Solubility in food simulants (3% acetic acid, and 90% ethanol) was performed for xylan and starch-based bioplastics. Bioplastic was evaluated to grow Aspergillus versicollor for xylanase production. The bioplastic was evaluated as a photoprotector with yeast exposed to UVC light-covered by the bioplastic for 2 h. Bioplastic disintegration was evaluated in different soil moistures and the disintegration on the surface of the compost. Liquid washes from soils exposed to bioplastic biodegradation were tested for Lactuca sativa seed germination/inhibition. Water from a local lake was exposed to bioplastic and microbial cell density modification was verified. Images of the surface of the bioplastics were obtained by scanning electron microscopy, and characterized by thermogravimetric and dynamic-mechanical analysis. The xylan addition in bioplastic led to a material with a 40–50% decreased ultraviolet light transmittance. An increase in xylan concentration reduced solubility in lipid food simulant solutions, with no fatty solubilization with 25% of xylan. It suggests potential applications in photoprotective and packaging contexts. The thermal degradation temperature of the pure starch bioplastic was 324 °C, and the addition of 10% (287 °C), 15% (286 °C), and 25% (296 °C) xylan (w/w) indicated a reduction in thermal resistance, possibly due to suboptimal interaction between polymer chains. The decrease in crystallinity in the compositions 10/90% (Xc = 20%), 15/85% xylan/starch (Xc = 21%) compared to 25/75% xylan/starch (Xc = 11%) also underscored the complexity of polymer interactions within the bioplastic matrix. Tensile strength of pure starch was 1.21 MPa, while the composition of 15/85% xylan/starch exhibited improved strength 2.99 MPa. Further investigation into the interaction between starch and xylan is warranted. Concerning the disintegration of the 25/75% xylan/starch formulation in the soil, the humidity of the soil matrix played a significant role. The disintegration occurred over 5 days and 16 days in compost (55% humidity) and soil (32.6% humidity), respectively. The results of phytotoxicity (Lactuca sativa seeds) and changes in the physicochemical and biological profile of water (smell, turbidity, phosphorus and nitrogen levels, pH, and bacterial and phytoplankton density/richness), in response to exposure to bioplastics, highlight the necessity of developing this biologically-based and biodegradable technology in concerns about potential environmental impacts. Furthermore, the present study introduces the approach of bioplastic waste recycling using enzyme production biotechnology. In line with the legitimacy of bioplastics as important materials for addressing the challenges posed by their non-biodegradable synthetic counterparts, the presented results broaden the discourse on the feasibility of this biologically based material, contributing to the development of a sustainable society.

The rigid-flexible balanced molecular crosslinking network transition interface: An effective strategy for improving the performance of bamboo fibers/poly(butadiene succinate-co-butadiene adipate) biocomposites

The poor interfacial compatibility of natural fiber-reinforced polymer composites has become a major challenge in the development of industry-standard high-performance composites. To solve this problem, this study constructs a novel rigid-flexible balanced molecular crosslinked network transition interface in composites. The interface improves the interfacial compatibility of the composites by balancing the stiffness and strength of the fibers and the matrix， effectively improving the properties of the composites. The flexural strength and flexural modulus of the composites were enhanced by 38 % and 44 %, respectively. Water absorption decreased by 30 %. The initial and maximum thermal degradation temperatures increased by 20 °C and 16 °C, respectively. The maximum storage modulus increased by 316 %. Furthermore, the impact toughness was elevated by 41 %, attributed to the crosslinked network's efficacy in absorbing and dissipating externally applied energy. This innovative approach introduces a new theory of interfacial reinforcement compatibility, advancing the development of high-performance and sustainable biocomposites.

An antibacterial film using κ-carrageenan loaded with benzyl isothiocyanate nanoemulsion: Characterization and application in beef preservation

Benzyl isothiocyanate (BITC) is a naturally active bacteriostatic substance and κ-carrageenan (KC) is a good film-forming substrate. In the present study, a nanoemulsion incorporating BITC was fabricated with a particle size of 224.1 nm and an encapsulation efficiency of 69.2 %. Subsequently, the acquired BITC nanoemulsion (BITC-NE) was incorporated into the KC-based film, and the light transmittance of the prepared composite films was lower than that of the pure KC film. Fourier transform infrared spectroscopy and scanning electron microscopy revealed that BITC-NE was compatible with the KC matrix. BITC-NE incorporation enhanced the tensile strength of the KC-based films by 33.7 %, decreased the elongation at break by 33.8 %, decreased the water vapor permeability by 60.1 %, increased the maximum thermal degradation temperature by 48.8 %, and decreased the oxygen permeability by 42 % (p < 0.05). Furthermore, the composite films showed enhanced antimicrobial activity against Staphylococcus aureus, Salmonella typhimurium, and Pseudomonas fluorescens. The developed KC-based composite films were applied to wrap raw beef, which significantly delayed the increase in total viable count, total volatile base nitrogen content, and thiobarbituric acid reactive substances, and prolonged the shelf-life of the raw beef by up to 10 days. These results indicated that the composite films prepared by incorporating BITC nanoemulsions into KC matrices have great antimicrobial application potential.

Biodiesel derived from the microalgae Nannochloropsis gaditana and Haematococcus pluvialis: Physicochemical and tribological properties

The physicochemical and tribological propertie of two biodiesels derived from Nannochloropsis gaditana and Haematococcus pluvialis microalgae were evaluated, and the impact of their fatty acid methyl esters (FAMEs) on the aforementioned properties was also evaluated. The H. pluvialis biodiesel exhibited reduced friction and wear compared to the N. gaditana counterpart, attributed to its lower degree of unsaturation and higher content of chain length of 17–18, which enhances the adsorption of stronger and thicker tribofilms. Additionally, the higher ratio of monounsaturated to total saturated FAME content contributed to this outcome. The content of polyunsaturated fatty acids decreased the viscosity and increased the end thermal degradation temperature.

Obtaining cellulose nanocrystals by acid hydrolysis procedure; and their use as reinforcement in polylactide biocomposites

In the first step of this study, purpose was to obtain and characterize cellulose nanocrystal (CNC) particles by applying sulfuric acid hydrolysis method to the starting material of microcrystalline cellulose (MCC) fibrils. After obtaining CNC particles via acid hydrolysis procedure, various analyses (SEM, DLS, FTIR, XRD, TGA) conducted revealed that average size of round shaped CNC particles was 38 nm with −30.4 mV Zeta potential value. They had monoclinic Cellulose-I crystal structure with Crystallinity Index of 80.6% and Crystallite Size of 3.39 nm. Their maximum thermal degradation temperature was 307°C with 23 wt% residue at 800°C. In the second step, the main aim was to investigate contribution of these obtained CNC particles when they were used as nano-reinforcement in polylactide (PLA) matrix biocomposites produced by industrially compatible melt mixing and shaping techniques. Mechanical tests revealed that when only 1 wt% CNC particles were incorporated into PLA matrix, increases in flexural strength and modulus were 29% and 51%; while increases in K IC and G IC fracture toughness values were 42% and 105%, respectively. Because, high degree of hydroxyl groups and presence of sulfate half-ester groups on the surfaces of CNC particles improved the interfacial interactions between the matrix and nano-reinforcement phase, leading to efficiency in strengthening and toughening mechanisms.

Ionic liquid pretreatment of lignocellulose for complete hemicellulose removal to produce high-purity cellulose mixed esters

Strategic valorization of agricultural waste can serve as waste management and promote sustainable biorefineries. Sugarcane bagasse is a readily available lignocellulosic biomass and can be converted into valuable cellulose-based thermoplastics. However, the cellulose purity significantly influences the material properties of the resulting thermoplastics, potentially limiting their applications. Therefore, conventional production necessitates harsh pretreatment of lignocellulose to isolate high-purity cellulose, followed by chemical modification. Here, we demonstrate a facile and green pretreatment method for complete removal of hemicellulose by incubating bagasse in a mixed system of an ionic liquid, 1-ethyl-3-methylimidazolium acetate (EmimOAc), and dimethyl sulfoxide (DMSO) at 140 °C, followed by precipitation in water, achieving >99 % hemicellulose removal. The pretreated bagasse, containing 71 % cellulose and 28 % lignin, underwent homogeneous transesterification with vinyl decanoate and isopropenyl acetate, using EmimOAc as both the solvent and catalyst, assisted by a co-solvent of DMSO. The polysaccharide derivative in the resulting acylated bagasse was separated from the lignin derivative by precipitation in methanol. The obtained polysaccharide derivative with high cellulose purity displayed a high weight-average molar mass of 1.5×106 g mol−1 and a polydispersity of 4. It also exhibited superior thermal stability (thermal degradation temperature, Td−5 %: 359 °C; glass transition temperature, Tg: 144 °C) compared to pulp-derived cellulose acetate decanoate (Td−5 %: 349 °C; Tg: 129 °C).

Morphological, TGA, and FTIR on Rigid Polyurethane Composite Laminated with Untreated and Treated Bamboo Fiber Roof Insulation

The performance of roof insulation such as polyurethane decreased due to problems such as insufficient absorption and poor thermal insulation performance, especially during rainstorms. The aims of this study are to investigate the physical property and its potential reinforced material such as rigid polyurethane doped with treated and untreated bamboo fiber composite (RPU-BF) at different ratios of 0, 25, 30, 35, and 40% of bamboo fibers as an insulation material for roof applications. The bamboo fibers were treated by using silane coupling agent treatment. The rigid polyurethane composite samples were prepared and then laminated bamboo fiber to overcome the sound problem in roofs. The physical characterization was investigated by Water Contact Angle (WCA), the morphological by Scanning Electron Microscopy (SEM), Thermo-gravimetric Analysis (TGA), and Fourier Transform Infrared Spectroscopy (FTIR) Analysis. The results showed that the treated bamboo fiber had a 192.5° water contact angle as a super hydrophobic property due to the presence of the chemical bonds Si-O-Si and Si-O-C in the silane coupling agent treatment. The morphology showed that 30% ratios of RPU-BF-T30 give the smallest pore diameter size. The peak of thermal degradation temperature of untreated and treated bamboo fiber was increased from 320°C to 350 °C with a weight loss of 80% to 50%. The treated bamboo fiber exhibited peaks at 3010–3040 cm-1 were associated with stronger Si-O-Si bonding, indicating the formation of new chemical bonds between bamboo fiber and silane coupling agent due to the ester bond from the cellulose, lignin, and hemicellulose. Thus, there was a similar trend peak in the functional chemical group in the FTIR spectrum of the RPU-BF composite. This result shows that RPU-BF composite had the potential of the optimum ratio of bamboo fiber as an insulation material for local communities and beneficial to the bamboo industry.

Characterization of natural cellulosic fiber extracted from Grewia ferruginea plant stem

The use of natural fibers as reinforcement in polymer composites has gained significant attention due to their eco-friendly, and biodegradability. This study aims to extract and characterize the natural cellulosic fibers from the Grewia ferruginea stem. The fibers were extracted from plant stems using sodium hydroxide and analyzed using Fourier Transform infrared spectroscopy (FTIR) to determine chemical bonds on the fiber and functional group and Thermos-gravimetric analysis (TGA) was used to determine the thermal stability and degradation temperature of the fiber. The crystalline properties of extracted fibers were characterized by x-ray diffraction and surface morphology was characterized by Scanning electron microscopy. The chemical composition of the fibers, including cellulose, hemicellulose, lignin, moisture, extractive content, and fiber linear density, was evaluated. Tensile, thermal, and FTIR studies were conducted to assess the performance properties of the extracted fiber. The analysis revealed that the Grewia ferruginea fibers contain cellulose (60.4–72.6 wt%), hemicellulose (18.5 ± 3.1 %), and lignin (13.55 ± 2.75 %). The extracted fibers have a crystallinity index of 48.76 % and crystallite size of 5.14 nm. The fiber exhibited tenacity, breaking elongation, and Young's modulus values of (52.3 ± 6.5 cN/tex), (3.6 ± 1.8 %), and 43.5 ± 2.3 GPa, respectively. FTIR studies confirmed the presence of biopolymers in the Grewia ferruginea fiber. Additionally, the fibers demonstrated thermal stability up to 275 °C based on thermogravimetric analysis. These findings suggest that the extracted natural cellulosic Grewia ferruginea fiber has the potential to be used as a sustainable reinforcement material in polymeric composites.

Robust shape memory chlorobutyl rubber/boron nitride polymer nanocomposites for oil-water separation application

BackgroundBoron nitride (h-BN), an excellent 2D material finds exceptional applications in various fields owing to its unique characteristics including excellent hydrophobicity. Incorporation of boron nitride in polymer matrices is a captivating strategy by the scientific community to tune the properties of polymer. Interestingly, the possibilities of incorporating h-BN in chlorobutyl rubber (CIIR) matrix has never been considered and tried till now. Moreover, the use of CIIR to create a clean environment and reduce water pollution is an unexplored area even though the CIIR rubber possess excellent barrier properties. MethodsIn this work, two techniques were used for the fabrication of BNNS/CIIR nanocomposite. We exfoliated h-BN via chemical exfoliation method and tried the reinforcement of CIIR with BNNS via solution intercalation method. Shape memory analysis was performed with the help of stearic acid and oil-water separation analysis was achieved through an easy experimental technique. Significant findingsEnhanced mechanical strength of 11.57 MPa, improved thermal degradation temperature and char yield, higher glass transition temperature of -45.98° were observed for BNNS/CIIR nanocomposite reinforced with higher BNNS loading owing to the uniform distribution and better intercalation of BNNS in CIIR. Excellent shape memory was exhibited by CIIR matrix when reinforced up to 5 g BNNS. In addition, the nanocomposites displayed excellent ability to perform oil-water separation with increase in BNNS loading owing to the good hydrophobic character of h-BN and inherent barrier properties of CIIR. Thus, the study proved successful towards the fabrication of advanced CIIR nanocomposites with excellent shape memory and oil water separation efficiency.

Andiroba Oil (Carapa guianensis Aubletet) as a Functionalizing Agent for Titica Vine (Heteropsis flexuosa) Nanofibril Films: Biodegradable Products from Species Native to the Amazon Region

The diversity of species in Amazonia is exceptionally vast and unique, and it is of great interest for industry sectors to explore the potential of derivatives with functional properties for packaging applications. This study proposes the functionalization of cellulose micro/nanofibril (MFC/NFC) suspensions from Heteropsis flexuosa with andiroba oil to produce films with packaging potential. MFC/NFC was produced by using mechanical fibrillation from suspensions of H. flexuosa fibers. Proportions of 1, 3, and 5% of andiroba oil were added to make films with concentrations of 1% (m/m). Suspensions with andiroba oil provided greater viscosity, with changes in the physical properties of the films. Functionalization with andiroba oil provided films with lower degradation in water, greater contact angle, and lower wettability despite high permeability to water vapor. The films with 1% andiroba oil showed a hydrophobic characteristic (contact angle &gt; 90°) and greater puncture resistance (6.70 N mm−1). Films with 3% oil showed a more transparent appearance and high biodegradation, while 1% oil generated more opaque films with a higher thermal degradation temperature and high antioxidant activity. It was concluded that films produced from H. flexuosa fibers functionalized with andiroba oil showed packaging potential for light, low-moisture products due to their adequate thermal and barrier characteristics.

Characterization of fly ash reinforced wood polypropylene composites

In this study, fly ash, which is released as waste from thermal power plants and has negative effects on the environment, was evaluated as a filler in wood-plastic composite materials (WPC). For this purpose, inorganic fly ash from thermal power plants was mixed with polypropylene (PP) thermoplastic polymer at 10%, 20%, 30%, 40%, and 50% by extrusion method instead of wood flour used in wood plastic composite materials. Maleic anhydride-treated polypropylene (MAPP) was used to strengthen the bonding during WPC production. The material mixed in extrusion was passed through a crusher and turned into pellets. Test samples were prepared using injection molding of pelletized WPC material. Density, thickness swelling, water absorption, modulus of rupture, impact strength, modulus of elasticity in bending, tensile strength, janka hardness, differential scanning calorimetry (DSC), and thermogravimetric analyses (TGA) were performed on the prepared test samples. The results indicated that as the amount of fly ash used in the wood-plastic composite material increases, the density increases but the thermal degradation temperature of the material, water uptake, the swelling ratio to its thickness, tensile strength, impact strength, janka hardness, modulus of rupture, and modulus of elasticity decrease.

Use of ozone oxidation in combination with deacetylation for improving the structure and gelation properties of konjac glucomannan

In this study, oxidized deacetylated konjac glucomannans with different degrees of oxidation were prepared by a combination of deacetylation and ozone oxidation. Carboxyl groups were found to be introduced into the modified konjac glucomannan while acetyl groups were removed. The backbone, branched chains, and crystal structure of modified konjac glucomannan were not significantly affected. The whiteness was enhanced to 97–99 % and the thermal degradation temperature was up to 250 °C after modification. The solubility of the modified konjac glucomannan (oxidized for 60 min) was significantly increased to 84.56 % (p < 0.05), while its viscosity and swelling power were notably decreased owing to the changes in molecular weight (from 106 to 104) and functional groups. Rheological analysis showed that oxidized deacetylated konjac glucomannan has the ability to form soft-textured gels and the potential to develop dysphagia foods. Future studies should focus on the gelation mechanisms of oxidized deacetylated konjac glucomannan.

Unveiling structure and performance of tea-derived cellulose nanocrystals

In this study, cellulose was extracted from black tea residues to produce black tea cellulose nanocrystals (BT-CNCs) using an optimized acid hydrolysis method. The structure and performance of BT-CNCs were evaluated. The results showed that the optimal conditions for acidolysis of BT-CNCs included a sulfuric acid concentration of 64 %, a solid-liquid ratio of 1:18 (w/v), a hydrolysis temperature of 45 °C, and a hydrolysis time of 50 min. The optimization process resulted in a 44.8 % increase in the yield of BT-CNCs, which exhibited a crystallinity of 68.57 % and were characterized by the typical cellulose I structure. The diameters of the particles range from 5 to 45 nm, and they exhibit aggregation behavior. Notably, BT-CNCs demonstrated excellent storage stability, and the Tyndall effect occurred when exposed to a single beam of light. Although the thermal stability of BT-CNCs decreased, their primary thermal degradation temperature remained above 200 °C. The colloidal nature of BT-CNCs was identified as a non-Newtonian fluid with “shear thinning” behavior. This study introduces a novel method to convert tea waste into BT-CNCs, increasing the yield of BT-CNCs and enhancing waste utilization. BT-CNCs hold promise for application in reinforced composites, offering substantial industrial value.

Processing and Evaluation of Bio-Based Paramylon Ester/Poly(butylene succinate) Blends for Industrial Applications

AbstractPoly(butylene succinate) (PBS) was melt-blended with paramylon based mixed ester, paramylon propionate hexanoate (PaPrHe) and characterized for its morphology, thermal and mechanical properties. The PBS/PaPrHe blends were found to be immiscible throughout the loading range of PaPrHe (10–90 wt%), with individual glass transition peaks. Due to the immiscibility, there was phase separation observed in the bulk, evident by sea-island morphology. However, further observation of the micro-structure revealed that, in low PaPrHe loading (10–30 wt%), there was a micron to sub-micron order distribution of PBS particles and partially miscible PBS/PaPrHe phase. On increasing the PaPrHe to 50 wt% and beyond, the sub-micron scale domains fused to form a co-continuous morphology. As a result, the impact strength of PBS increased from 6.6 to 16.4 kJ/m2 in the 50/50 blend. Under tensile loading, the strength at break and elongation decreased after the introduction of less-flexible PaPrHe particles in the blend. This could be countered by uniaxially stretching the blended films with 10–30 wt% PaPrHe, after which the tensile strength increased by up to 380% (from 33–52 MPa to 165–200 MPa) compared to the unstretched films, attributable to the increased degree of orientation of the molecular chains. In terms of thermal processability, all the blend ratios had high thermal degradation temperature (&gt;350 °C), higher than the melt-flow temperature (124–133 °C) providing a wide processing window. Overall, PBS/PaPrHe blend is a novel bio-based blend with properties suitable for packaging, mulching, and related applications.

Formation of amygdalin/β-cyclodextrin derivatives inclusion complexes for anticancer activity assessment in human cervical carcinoma HeLa cell line

Nanoencapsulation has gained considerable attention because of its unique features and advantages in anticancer drug delivery. Amygdalin (AMY) is an anticancer compound, showing limitations in its applications by low stability. Herein, the inclusion complexes (ICs) of AMY with β-cyclodextrin (βCD), and its derivatives such as 2-hydroxypropyl-βCD (HPβCD) and methyl-βCD (MβCD) were fabricated. The fabricated AMY/CD-ICs were thoroughly evaluated using Fourier-transform infrared spectroscopy, powder X-ray diffraction, thermogravimetric/differential thermal analysis, proton nuclear magnetic resonance, ultraviolet–visible diffuse reflectance spectroscopy, and photoluminescence techniques. Double reciprocal profile study of the absorption and fluorescence spectra revealed that the AMY formed the ICs with βCD derivatives at a guest/host stoichiometric ratio of 1/1. The thermal stability of AMY was enhanced as the IC formation aid observed by the shift of thermal degradation temperature of AMY from the range of ∼ 220–250 °C to > 295 °C. Theoretical analyses of the energetic, electronic, and global reactivity parameters of the AMY/CD-ICs were evaluated using the PM3 method. Further assessment of the dissolution diagrams of AMY/CD-ICs revealed a burst release profile. In addition, cell toxicity was evaluated using the MTT assay, and the results showed that AMY/CD-ICs had significantly more efficacious in inhibiting HeLa cancer cells than AMY. These results proved that the IC formations with CDs significantly enhanced the anticancer activity of AMY.

Bio-Based Thiol-ene Network Thermosets from Isosorbide and Terpenes.

Thermoset networks are chemically cross-linked materials that exhibit high heat resistance and mechanical strength; however, the permanently cross-linked system makes end-of-life degradation difficult. Thermosets that are inherently degradable and made from renewably derived starting materials are an underexplored area in sustainable polymer chemistry. Here, we report the synthesis of novel sugar- and terpene-based monomers as the enes in thiol-ene network formation. The resulting networks showed varied mechanical properties depending on the thiol used during cross-linking, ranging from strain-at-breaks of 12 to 200%. Networks with carveol or an isosorbide-based thiol incorporated showed plastic deformation under tensile stress testing, while geraniol-containing networks demonstrated linear stress-strain behavior. The storage modulus at the rubbery plateau was highly dependent on the thiol cross-linker, showing an order of magnitude difference between commercial PETMP, DTT, and synthesized Iso2MC. Thermal degradation temperatures were low for the networks, primarily below 200 °C, and the Tg values ranged from -17 to 31 °C. Networks were rapidly degraded under basic conditions, showing complete degradation after 2 days for nearly all synthesized thermosets. This library demonstrates the range of thermal and mechanical properties that can be targeted using monomers from sugars and terpenes and expands the field of renewably derived and degradable thermoset network materials.

Capsicum leaf protein-based bionanocomposite films for packaging application: Effect of corn starch content on film properties

The addition of corn starch (CS) enhances the interfacial adhesion of the film-forming liquids (FFLs), weakening the internal relative molecular motion. As a result, the rheological properties and zeta potential values of the FFLs were affected. A tight spatial network structure between capsicum leaf protein (CLP), lignocellulose nanocrystals (LNCs) and CS can be formed through intermolecular entanglement and hydrogen bonding interactions. The crystallinity, thermal degradation temperature, tensile strength and water contact angle of the protein-based bionanocomposite films (PBBFs) increased with increasing CS addition. This is due to the transformation of the secondary space structure of the CLP inside the PBBFs and the increase in cohesion. However, the excessive addition of CS forms aggregated clusters on the surface of PBBFs, which increases the surface roughness of PBBFs and causes more light scattering. Therefore, the brightness and yellowness values of the PBBFs increase, and the transmittance decreases.