Low Glass Transition Temperature Research Articles

Sequence-Controlled Copolymerization of Structurally Well-Defined Multinuclear Zinc Acrylate Complexes and Styrene.

The copolymerization of two or more monomers produces polymeric materials with unique properties that cannot be achieved with homopolymers. However, precise control over the polymer sequence remains challenging because the sequence is determined by the inherent reactivity of comonomers. Therefore, only limited methods using modified monomers or supramolecular interactions are reported. In this study, the sequence control of acrylate-styrene copolymerization using multinuclear zinc complexes is reported. The copolymerization of the zinc acrylate complex with a polymeric sheet-like structure and styrene in benzene affords a copolymer with a higher content of acrylate triad than calculated for the statistical random model, whereas tetranuclear zinc acrylate (TZA) affords a copolymer with fewer adjacent acrylate sequences. The copolymer with a higher content of acrylate triad exhibits a lower glass transition temperature because of the higher mobility of the longer polystyrene segments. These results highlight the promise of multinuclear zinc acrylate complexes as monomers for sequence-controlled copolymerization.

Smoothening Perfluoroalkylated Surfaces: Liquid‐Like Despite Molecular Rigidity?

AbstractThe rational design of surfaces at the molecular level is essential toward realizing many engineering applications. However, molecular‐scale defects affect processes such as triboelectrification, scaling, and condensation. These defects are often detectable via contact angle hysteresis (CAH) measurements. Liquid‐like surfaces exhibit extremely low CAH (≤5°) and rely on the use of highly flexible molecular species such as long‐chain alkyls or siloxanes. Their low glass transition temperatures lead to the so‐termed self‐smoothing behavior, reducing sensitivity to defects formed during fabrication. However, utilizing rigid molecular species such as perfluoroalkyl chains often results in higher hysteresis (10° to 60°) as defects are not self‐smoothed after fabrication. Consequently, state‐of‐the‐art perfluoroalkylated surfaces often show sub‐optimal interfacial properties. Here, a customizable chemical vapor deposition process creates molecularly‐thick, low‐defect surfaces from trichloro(1H,1H,2H,2H‐perfluorooctyl)silane. By implementing moisture‐exposure controls, highly homogenous surfaces with root‐mean‐square roughness below 1 nm are fabricated. CAH is achieved down to ≈4° (average: 6°), surpassing the state‐of‐the‐art by ≈5°. Reduction of CAH (26° to 6°) results in condensation suppression, decreasing surface droplet density by one order and surface droplet coverage by 40%. This work guides the synthesis of high‐quality surfaces from tri‐functional perfluoroalkylsilanes with liquid‐like properties despite their molecular rigidity.

Largely enhanced damping performance of nitrile rubber/ethylene–vinyl acetate blends via phenolic resin-induced phase separation

The low glass transition temperature (Tg) and narrow effective damping temperature range (EDTR) greatly restrict the application of common vulcanized rubbers in fields relating to high temperature environmental condition due to the greatly reduced damping performances. In this work, phenolic resin (PR) was incorporated into nitrile rubber/ethylene–vinyl acetate (NBR/EVM) blends through melt-compounding processing, and the microstructure and damping performance changes induced by PR were comparatively investigated. The results show that PR induces the phase separation of the blends and most of PR particles selectively locate in the NBR component. Molecular dynamics simulation confirms that more hydrogen bonds form in the ternary blends, and reduced free volume fraction is also achieved. The ternary blends show good high-temperature damping performances, and apparently enhanced Tg (up to 17.7 °C) and EDTR (82.6 °C, from −2.6 to 80 °C) are also achieved. Additionally, the ternary blends exhibit good mechanical properties, including higher ductility and larger fracture energy, and better energy dissipation ability. This work provides an alternative resolution way to enhance the damping performances of the common vulcanized rubbers at high temperatures.

Enantiomorphic Site-Assisted Chain End Control Stereospecific Alternating Copolymerization of Chiral Cyclic Diesters.

Stereospecific alternating copolymerization of different chiral cyclic esters is one feasible approach to enrich the structural diversity of copolyesters and tailor their properties. However, dramatically different reactivities of different cyclic esters let a perfectly stereospecific alternating polymerization of these cyclic esters be a challenge, thus the catalyst is required to balance their reactivities. Herein, a remarkable enantiomorphic site effect on chain end control was discovered and successfully utilized to balance the reactivities of highly reactive S, S-lactide (S, S-LA) and low reactive R, R-ethylglycolide (R, R-EG)/R, R-propylglycolide (R, R-PG) during their heterospecific alternating copolymerization. The enantiomorphic site of R, R-SalenAl complex can increase the relative reactivity of R, R-EG/R, R-PG and suppress that of S, S-LA, then a perfectly alternating sequence of the copolymer of S, S-LA and R, R-EG/R, R-PG can be achieved (Palt = 0.96/0.91); inversely, using S, S-SalenAl complex, the significant enantiomorphic site effect enlarges the reactivity difference of two monomers, the alternating level was just 0.70/0.68 even to 0.61. Poly(S, S-LA-alt-R, R-EG) with a high alternating regularity exhibits lower glass transition temperatures and a dramatically higher elongation at break (εB = 449 ± 51% (Palt = 0.96) vs εB = 6 ± 1% (Palt = 0.70)).

Enantiomorphic Site‐Assisted Chain End Control Stereospecific Alternating Copolymerization of Chiral Cyclic Diesters

Stereospecific alternating copolymerization of different chiral cyclic esters is one feasible approach to enrich the structural diversity of copolyesters and tailor their properties. However, dramatically different reactivities of different cyclic esters let a perfectly stereospecific alternating polymerization of these cyclic esters be a challenge, thus the catalyst is required to balance their reactivities. Herein, a remarkable enantiomorphic site effect on chain end control was discovered and successfully utilized to balance the reactivities of highly reactive S, S‐lactide (S, S‐LA) and low reactive R, R‐ethylglycolide (R, R‐EG)/R, R‐propylglycolide (R, R‐PG) during their heterospecific alternating copolymerization. The enantiomorphic site of R, R‐SalenAl complex can increase the relative reactivity of R, R‐EG/R, R‐PG and suppress that of S, S‐LA, then a perfectly alternating sequence of the copolymer of S, S‐LA and R, R‐EG/R, R‐PG can be achieved (Palt = 0.96/0.91); inversely, using S, S‐SalenAl complex, the significant enantiomorphic site effect enlarges the reactivity difference of two monomers, the alternating level was just 0.70/0.68 even to 0.61. Poly(S, S‐LA‐alt‐R, R‐EG) with a high alternating regularity exhibits lower glass transition temperatures and a dramatically higher elongation at break (εB = 449 ± 51% (Palt = 0.96) vs εB = 6 ± 1% (Palt = 0.70)).

High rubber elasticity and thermal conductivity in plasticized polyvinyl chloride film with flame retardancy and smoke suppression properties

AbstractFor hydrogenated nitrile‐butadiene rubber (HNBR) modified polyvinyl chloride (PVC), magnesium hydroxide and antimony trioxide are frequently employed as flame retardants. Fume silica is thought to be useful reinforced agent for rubber as well as efficient flame retardant for polymer‐based composites. The plasticized PVC and HNBR blend in this work were combined with three fillers mentioned above to create rubber‐plastic composites that performed well overall, with a notable improvement in combustion. The limiting oxygen index of the composites increased from 23.7% to 33.8% with no droplets falling during combustion, the smoke density rating decreased from 23.8% to 7.9%, and the maximum smoke density dropped from 95.5% to 15.5%. The cone calorimetry test findings revealed that the three fillers simultaneously prevented the emission of smoke and heat from combustion. High thermal conductivity is typically linked to excellent flame retardancy. The thermal conductivity of composites rose from 0.193 to 0.583 W m−1 K−1 with the addition of fillers. Furthermore, the low glass transition temperature and permanent set of improved composites reflect its softness and rubber elasticity. Thermogravimetric analysis was used to examine the thermal stability of the composites in nitrogen and air, and the results indicated the addition of fillers improved the thermal stability.

On the Electrochemical Properties of Poly(Vinylidene Fluoride)/Polythiophene Blends Doped with Lithium‐Based Salt

AbstractIn this study, polymer blends of polythiophene (PTH) and poly(vinylidene fluoride) (PVDF) are investigated by focusing on their structural and electrochemical characteristics. These blends displayed immiscibility confirmed through field emission scanning electron microscopy (FE‐SEM) and interaction assessments. PTH's role as a plasticizer is evident, diminishing crystallinity. A rise in PTH level led to a lower glass transition temperature and a higher melting point, suggesting reduced intermolecular forces and increased polymer chain flexibility. Conversely, a dispersed phase presence elevated the melting point, restricting chain movement and crystallization. The thermal properties of blends are enhanced by increased PTH content. Applying the Vogel–Tammann–Fulcher model to ionic conductivity measurements, it observed a direct relationship between temperature and free volume, impacting conductivity and ion transport numbers. Certain materials exhibit increased activation energies, indicating substantial thermodynamic barriers to local motion. Higher PTH content within the PVDF matrix notably increased the lithium ion transfer number from 0.22 to 0.71, a change tied to the C–S–C structure of polythiophene. However, elevated PTH levels also led to diminished negative charge transfer and ionic conductivity in the PTH‐PVDF blend compared to pure PVDF, likely due to an ionic conduction hindrance.

Impact of UV Light Exposure During Printing on Thermomechanical Properties of 3D-Printed Polyurethane-Based Orthodontic Aligners

Aim: Polyurethane-based aligners, created through photoinitiated free-radical polymerization, have been the subject of numerous studies focusing solely on their mechanical properties. In contrast, we investigate their thermomechanical properties, which are crucial for their efficacy. This paper aims to investigate the effects of different UV light exposure durations on the complex modulus of elasticity, tan delta, glass transition temperature, and the degree of conversion (DC). Methods: Aligners were printed using Tera Harz TC-85 and NextDent Ortho Flex resin with specific exposure times (2, 2.4, 3, 4, and 4.5 s for Tera Harz; 5, 6, 7, and 8 s for NextDent) and processed per manufacturer guidelines. The degree of conversion was analyzed using Attenuated Total Reflectance Fourier Transform Infrared (ATR-FTIR) spectroscopy, while Dynamic Mechanical Analysis (DMA) characterized the mechanical properties (complex modulus and tan delta) and the glass transition. Results: Tera Harz TC-85 showed a higher degree of conversion (90.29–94.54%), suggesting fewer residual monomers, which is potentially healthier for patients. However, its lower glass transition temperature (35.60–38.74 °C) might cause it to become rubbery in the mouth. NextDent Orto Flex, with a higher storage modulus (641.85–794.55 MPa) and Tg (49.36–50.98 °C), offers greater rigidity and stability at higher temperatures (greater than temperature in the oral cavity), ideal for orthodontic forces, though its lower degree of conversion raises health concerns. Conclusions: Tera Harz TC 85 generally achieves higher DC and more stable polymerization across different UV exposure times than NextDent Orto Flex. Optimal polymerization times significantly impact both the mechanical and thermal properties of these dental resins, with NextDent showing optimal properties at 7 s and Tera Harz benefiting from both very short and extended exposure times.

Performance of RC beams strengthened using NSM FRP and cement based adhesives after exposure to elevated temperatures

A popular method for strengthening of reinforced concrete (RC) structures is the use of carbon fiber reinforced polymers (CFRP) bonded to the structural elements using the near surface mounted (NSM) techniques. While this method possesses many advantages, poor fire resistance as a result of the low glass transition temperatures (TG) of organic resins remains a significant drawback. Replacement of organic resins with cement based adhesives (CBA) could potentially improve the fire performance of NSM FRP systems and reduce the amount of insulation required to achieve the required fire endurance period. This paper presents an experimental program consisting of fifteen RC beams strengthened in flexure using NSM FRP bonded using CBA and subjected to the standard fire time temperature curve up to a target temperature of 600 °C. Twelve of the beams were strengthened using NSM-FRP laminates and bars including both smooth and rough FRP laminates and the remaining three specimens acted as control beams. Further, the use of plasterboard was explored as fire protection to further increase the residual strength of the specimens after heating. Results showed that the reinforced concrete beams strengthened with NSM CFRP retained 82 % to 61 % of their unheated strengthened ultimate load after heat exposure. This was a result of the superior performance of the cement-based adhesive at high temperature and the fire protection provided to the CFRP through embedment in the grooves. Moreover, the use of plasterboard as fire protection decreased the CFRP temperature by 42–24 %. The insulated beams behaved similarly to strengthened beams prior to fire exposure.

CO2-based polyurethane elastomers with enhanced mechanical and tunable room-temperature damping performances

Elastomers provide excellent damping performance owing to their unique viscoelasticity, which are widely used as vibration and noise reduction materials. However, conventional rubber-based elastomers with a low glass transition temperature (Tg) and narrow damping range are difficult to adapt to room-temperature conditions. Additionally, most of petroleum-based elastomers hinder the sustainable development. In this work, a series of novel polyurethane elastomers was synthesized using carbon-fixed CO2-based polycarbonate propylene diol (PPCD). The impact of hard segment (HS) content on the thermal, mechanical, and damping properties of CO2-based polyurethane (PU) was comprehensively investigated. Increasing the HS content from 16 % to 44 % increased the Tg from −3.8 °C to 21.7 °C, covering the entire damping range at room temperature with an adjustable damping performance. Furthermore, the tensile strength increased from 7.2 MPa to 27.0 MPa. The synthesis of CO2-based PU can propel the utilization of PU in damping applications, enabling sustainable advancement of the PU industry.

Structural and Dynamical Effects of the CaO/SrO Substitution in Bioactive Glasses.

Silicate glasses containing silicon, sodium, phosphorous, and calcium have the ability to promote bone regeneration and biodegrade as new tissue is generated. Recently, it has been suggested that adding SrO can benefit tissue growth and silicate glass dissolution. Motivated by these recent developments, the effect of SrO/CaO-CaO/SrO substitution on the local structure and dynamics of Si-Na-P-Ca-O oxide glasses has been studied in this work. Differential thermal analysis has been performed to determine the thermal stability of the glasses after the addition of strontium. The local structure has been studied by neutron diffraction augmented by Reverse Monte Carlo simulation, and the local dynamics by neutron Compton scattering and Raman spectroscopy. Differential thermal analysis has shown that SrO-containing glasses have lower glass transition, melting, and crystallisation temperatures. Moreover, the addition of the Sr2+ ions decreased the thermal stability of the glass structure. The total neutron diffraction augmented by the RMC simulation revealed that Sr played a similar role as Ca in the glass structure when substituted on a molar basis. The bond length and the coordination number distributions of the network modifiers and network formers did not change when SrO (x = 0.125, 0.25) was substituted for CaO (25-x). However, the network connectivity increased in glass with 12.5 mol% CaO due to the increased length of the Si-O-Si interconnected chain. The analysis of Raman spectra revealed that substituting CaO with SrO in the glass structure dramatically enhances the intensity of the high-frequency band of 1110-2000 cm-1. For all glasses under investigation, the changes in the relative intensities of Raman bands and the distributions of the bond lengths and coordination numbers upon the SrO substitution were correlated with the values of the widths of nuclear momentum distributions of Si, Na, P, Ca, O, and Sr. The widths of nuclear momentum distributions were observed to soften compared to the values observed and simulated in their parent metal-oxide crystals. The widths of nuclear momentum distributions, obtained from fitting the experimental data to neutron Compton spectra, were related to the amount of disorder of effective force constants acting on individual atomic species in the glasses.

The influence of myrcene on anionic copolymerization of 1,3-pentadiene and styrene

C5-dienes including 1,3-pentadiene (PD) and isoprene (IP) as by-products of naphtha cracking are important industrial raw materials for the production of thermoplastic elastomers, synthetic rubber and resins. The research on living anionic polymerization (LAP) of myrcene (MY) is also of great significance for the development of new bio-based materials and products. Focusing on the optimal utilization of C5 resources and the high-value utilization of biomass resources and the realization of green chemical production, this article reports the synthesizing of a novel terpolymer by LAP of PD, styrene (ST) and the biomass monomer MY. The discovery of the alternating sequence structure of ST and PD inspires us to further explore the development of copolymers containing this unique sequence structure. The special long branched side chain of MY and its low glass transition temperature are also conducive to the synthesis of new integrated rubbers. The 1H NMR tracking analysis indicates that the polymerization pattern changes from alternating sequence to gradient block sequence with the increase of MY content. Combined with FTIR analysis, the PD monomeric units are mainly trans-1,4 structure and MY monomeric units are predominant cis-1,4 structure. Considering the extremely high polymerization activity of MY compared to ST and PD, the copolymerization rate is significantly dependent on the concentration of the PD monomer. Despite this, due to the interactions between ST and PD ([ST¦PD] intermediate), ST still tends to form alternating segments with PD. The ternary copolymerization can be viewed as a “binary gradient copolymerization” of [ST¦PD] and MY (rMY > r[ST¦PD]).

Synthesis and evaluation of bio-based Poly(oxime-urethane) with intrinsic antimicrobial properties

Intrinsic antimicrobial properties can give polyurethanes a wider range of applications. In this work, the bio-based chain extender, 2,5-diformylfuran dioxime (DFFD) possessing antimicrobial characteristic, is used to synthesize the intrinsically antimicrobial poly(oxime-urethane) (Dx-PU) with isophorone diisocyanate (IPDI) and poly(tetramethylene glycol) (PTMG-1000), and its properties are investigated. The results show that the tensile strength is 19.12 ± 0.49 MPa, the Young’s modulus of the poly(oxime-urethane) is 118.70 ± 11.40 MPa. The elongation at break and Shore A hardness were 292 ± 11 % and 93 ± 2, respectively. Additionally, the Dx-PU demonstrated a high thermal decomposition temperature of over 250 °C and a low glass transition temperature of the soft segments at approximately −60 °C. Meanwhile, research on Dx-PU coating has demonstrated that Dx-PU coating is 100 % antimicrobial against E. coli and S. aureus, and is suitable for use on a wide range of substrates, including glass, engineering plastics, metal and leather with excellent adhesion (ISO 0), pencil hardness (2H), impact resistance (0.5 m·kg) and flexibility (2 mm). The Dx-PU coating also has significant antibacterial performance in everyday environments. The outstanding flexibility, moderate Young’s modulus, high elongation at break, good thermal resistance, and excellent antimicrobial performance of Dx-PU make it highly suitable for applications on high-contact surfaces such as hospital walls, public sanitation facilities, countertops, and door handles. As a bio-based chain extender from renewable sources, DFFD offers new solutions for the synthesis of bio-based antimicrobial polyurethane and its coatings.

Low-Temperature and High-Rate Rechargeable Aluminum Batteries Enabled by Ternary Eutectic Electrolytes.

Rechargeable aluminum batteries (RABs) have garnered extensive scientific attention as a promising alternative chemistry due to the inherent advantages associated with aluminum (Al) metal anodes, including their high theoretical capacities, cost-effectiveness, environmental friendliness, and inherent non-flammable properties. Nonetheless, the practical energy density of RABs is constrained by the electrolytes that support lower operational voltage windows. Herein, we report a ternary eutectic electrolyte composed of 1-ethyl-3-methylimidazolium chloride ([C2C1im]Cl):1-butyl-3-methylimidazolium chloride ([C4C1im]Cl):aluminum chloride (AlCl3) for the application of RABs. The electrolyte exhibits a high operational potential window (~3V vs. Al/Al3+ on SS 316) and high ionic conductivity (~8.3 mS.cm-1) while exhibiting only a low temperature glass transition at -65 oC suitable for all-climate conditions. Al||graphene nanoplatelets cell delivers a high capacity of ~117 mAh/g, and ~43 mAh/g at a very high current densities of 1A/g and 5A/g, respectively. The cells render a reversible capacity of 20 mAh/g at -20 oC and 17 mAh/g at -40 oC, indicating their suitability for operation under extreme environmental conditions. We comprehensively evaluated the design and optimization of carbon paper-based battery systems. The ternary eutectic electrolyte demonstrates exceptional electrochemical performance, thus signifying its substantial potential for utilization in high-performance energy storage systems in all climates.

Study on UV-Curable Acrylic Clear Viscoelastic Materials with Grafted Structures

Flexible substrates are crucial for wearable electronic strain sensors, but achieving biocompatibility, low cost, and aesthetic appeal alongside good mechanical performance remains challenging. Acrylic-based clear viscoelastic films (CVFs) are gaining attention due to their excellent transparency and potential for enhanced mechanical properties. This study synthesized copolymers CVF1-4 with varying branch content using soft monomers 2-ethylhexyl acrylate (2-EHA), butyl acrylate (n-BA), and functional monomer acrylic acid (AA). Employing a "grafting-through" strategy, small molecule monomers, ATRP-synthesized oligomer pBA25, and photoinitiator 1,6-hexanediol diacrylate (HDDA) were in-situ polymerized under UV light to form transparent, flexible elastic films CVF1-4. Between -20 to 80 C, CVF1-4 demonstrated excellent mechanical properties such as low modulus (in the kPa range), low glass transition temperature (below -20 C), large deformation (500-600%), and high strain recovery rate (>95%). Among them, CVF3 with 15% branching showed a balanced comprehensive performance, exhibiting primarily elastic behavior at room temperature. Therefore, selecting appropriate molecular composition and grafting structure provides a simple and customizable solution for optimizing CVF properties.

Bioderived Thiol-Ene Emulsion Polymerization for Hybrid Latex Particles.

The thiol-ene emulsion polymerization of three dienes synthesized from bioderived compounds, and subsequent preparation of core-shell polymer latexes, is reported. Levoglucosan (LGA), levogucosenone (LGO) and isosorbide were first modified with 4-pentenoic acid to install polymerizable groups. These monomers were used along with a dithiol to prepare poly(thioether) particles via ab initio emulsion polymerization using potassium persulfate as initiator and sodium dodecyl sulfate as surfactant. The structure of the diene significantly influenced the size of the resulting polymer latex particles. Given their low glass transition temperature, the LGA-derived poly(thioether) particles were used as a seed for the seeded emulsion polymerization of either styrene or methyl methacrylate. Core-shell latex particles with a high Tg core and a low Tg bioderived shell were formed, as verified by electron microscopy and in agreement with theoretical predictions of the equilibrium particle morphology based on the interfacial tensions of each particle phase.

A Study on the Application of Lining Adhesives to Canvas Reinforcement Treatment(Patching)

Canvas patching utilizes various adhesives for localized reinforcement treatment, yet evaluations of their properties remain insufficient. This study presents surface changes and physical properties observed when seven types of lining adhesives, selected from prior research, were applied. Evaluations included contact angles, color changes, surface alterations, and tensile strength. Results indicated that glue paste was highly susceptible to moisture and exhibited decreased flexibility with environmental changes, while Beva film showed the most significant reduction in adhesion. Both glue paste and Beva film were sensitive to color changes, primarily displaying yellowing and browning. Plextol B500 demonstrated the greatest increase in adhesion and flexibility under environmental stress. Welding powder exhibited high adhesion but lower strain rates, causing notable deformations across the canvas. Within the same adhesive composition, higher hydrophilicity correlated with reduced yield stress and maximum strain, suggesting that hydrophilicity affects adhesion and flexibility. Adhesives with lower thermal decomposition and glass transition temperatures experienced greater changes in adhesion and flexibility. Rapid changes in adhesion following localized reinforcement treatment can lead to issues like peeling of reinforcing fabric or deformation of the canvas.

Dual drug release profiles of salicylate-based polymers and encapsulated chlorhexidine as potential periodontitis treatments

Salicylate-based poly(anhydride-esters; SAPAEs) have demonstrated wound healing properties due to salicylic acid (SA) release during polymer degradation. Additionally, the polymers are deformable and self-adhesive due to their low Young’s modulus, lower glass transition temperature ( Tg), and inherent tackiness at body temperature. These properties make them particularly well-suited for therapeutic use in the bacteria-laden environment of the oral cavity. To enhance their therapeutic capabilities, the antiseptic chlorhexidine dihydrochloride was physically incorporated into SAPAEs for dual release of antiseptic and anti-inflammatory upon degradation. This study analyzes the thermomechanical properties of two SAPAE compositions (adipate homopolymer and 50:50 adipate:sebacate copolymer) and the release of chlorhexidine (incorporated at 10% (w/w)) from these polymers. Polymer adhesivity was monitored as a function of chlorhexidine incorporation and in vitro degradation time. Throughout in vitro degradation, the polymer systems had a low Young’s modulus and a Tg at or near body temperature. Incorporation of the antiseptic further decreased Young’s modulus and increased both the Tg and adhesivity. The release profiles were also evaluated and determined to be similar for the homopolymer and copolymer, although the homopolymer degradation occurred over a longer time period. Overall, the SAPAE systems have favorable properties for periodontal disease treatments by virtue of their controlled degradability, deformability, adhesivity, and release profiles with encapsulated antiseptic.

Development of fish gelatin film for anti-fogging mushroom packaging

Mushrooms are extremely perspiring and transpiring commodities. The commonly used plastic films for packaging fresh mushrooms have lower water vapour permeability compared to the rate at which mushrooms transpire, resulting in excessive moisture accumulation inside the package which leads to fogging. This study aimed to investigate the properties of a fish scale gelatin-based film and its correlation with antifogging properties. To produce the gelatin-based film, gelatin was extracted from fish scales using chemical pretreatment and thermal denaturation of collagen. A film-forming solution (FFS) was prepared by dissolving 2% (w/v) gelatin in a solvent, with the addition of glycerol. The solution was then cast to form the film, which underwent tests for mechanical strength, thermal behaviour, barrier properties, and antifogging performance. The resulting film (G-Gly) exhibited reduced tensile strength (13.21 MPa) but increased elongation at break (82.4%). Differential scanning calorimetry revealed a lower glass transition temperature (59.91 °C) for G-Gly. Both gelatin films displayed high water vapour permeability (1.69–3.09x10-6 g m/m2.day.Pa), preventing condensation. Notably, the G and G-Gly films remained fog-free even under varying temperatures, unlike linear low-density polyethylene film (LLDPE). In conclusion, the gelatin-based films demonstrated strong barrier properties and effective antifogging capabilities, making them suitable for moisture-sensitive commodities like mushrooms.

Poly(1,12-dodecylene 5,5′-isopropylidene-bis(ethyl 2-furoate))-based sulfonated copolyesters: Effect of ionic groups and long chain aliphatic spacer on their thermo-mechanical properties, hydrodegradability and liquid water sorption

Poly (1,12-dodecylene 5,5′-isopropylidene-bis(ethyl 2-furoate)) has recently been introduced to the polymer field as an exceptionally flexible polyester derived from bio-based and cost-effective monomers. A partially sulfonated version of this polymer is prepared in this study by copolymerization with sulfonated isophthalic acid. A series of sulfonated bisfuranic-aromatic copolyesters PDDbFXSIY, containing up to 50 mol% of sulfonated moieties was synthesized, for the first time, using the 1,12-dodecandiol as a comonomer. Their chemical structure was investigated by FTIR and NMR (1H and 13C) spectroscopy. In terms of properties, these copolyesters showed high thermal stability (c.a. Td,max ≥ 350 °C), a low glass transition temperature and they were found to be amorphous up to 20 mol% of the sulfonated unit content. Hydrodegradability tests on PDDbFXSIY films carried out under alkaline conditions revealed highly stable materials even with increasing amount of sulfonated units. In addition, the films exhibit good liquid water sorption, which increases as the amount of sulfonated groups decreases, following the opposite trend of previously reported sulfonated bisfuranic-aromatic copolyesters prepared using short-aliphatic chain diols. These properties are obviously related to the concurrently incorporation of a dodecylene chain and sulfonated groups in the same backbone, making it possible to generate new hydrolytically stable bisfuran-based polymers with a sorption feature.