Mechanical Properties Of Films Research Articles

A Stretchable and Tough Graphene Film Enabled by Mechanical Bond.

The pursuit of fabricating high-performance graphene films has aroused considerable attention due to their potential for practical applications. However, developing both stretchable and tough graphene films remains a formidable challenge. To address this issue, we herein introduce mechanical bond to comprehensively improve the mechanical properties of graphene films, utilizing [2]rotaxane as the bridging unit. Under external force, the [2]rotaxane cross-link undergoes intramolecular motion, releasing hidden chain and increasing the interlayer slip distance between graphene nanosheets. Compared with graphene films without [2]rotaxane cross-linking, the presence of mechanical bond not only boosted the strength of graphene films (247.3 vs 74.8 MPa) but also markedly promoted the tensile strain (23.6 vs 10.2%) and toughness (23.9 vs 4.0 MJ/m3). Notably, the achieved tensile strain sets a record high and the toughness surpasses most reported results, rendering the graphene films suitable for applications as flexible electrodes. Even when the films were stretched within a 20% strain and repeatedly bent vertically, the light-emitting diodes maintained an on-state with little changes in brightness. Additionally, the film electrodes effectively actuated mechanical joints, enabling uninterrupted grasping movements. Therefore, the study holds promise for expanding the application of graphene films and simultaneously inspiring the development of other high-performance two-dimensional films.

A Stretchable and Tough Graphene Film Enabled by Mechanical Bond

The pursuit of fabricating high‐performance graphene films has aroused considerable attention due to their potential for practical applications. However, developing both stretchable and tough graphene films remains a formidable challenge. To address this issue, we herein introduce mechanical bond to comprehensively improve the mechanical properties of graphene films, utilizing [2]rotaxane as the bridging unit. Under external force, the [2]rotaxane cross‐link undergoes intramolecular motion, releasing hidden chain and increasing the interlayer slip distance between graphene nanosheets. Compared with graphene films without [2]rotaxane cross‐linking, the presence of mechanical bond not only boosted the strength of graphene films (247.3 vs 74.8 MPa) but also markedly promoted the tensile strain (23.6 vs 10.2%) and toughness (23.9 vs 4.0 MJ/m3). Notably, the achieved tensile strain sets a record high and the toughness surpasses most reported results, rendering the graphene films suitable for applications as flexible electrodes. Even when the films were stretched within a 20% strain and repeatedly bent vertically, the light‐emitting diodes maintained an on‐state with little changes in brightness. Additionally, the film electrodes effectively actuated mechanical joints, enabling uninterrupted grasping movements. Therefore, the study holds promise for expanding the application of graphene films and simultaneously inspiring the development of other high‐performance two‐dimensional films.

Physicochemical properties of active films of rose essential oil produced using soy protein isolate-polyphenol conjugates for cherry tomato preservation

Soy protein isolate (SPI)-polyphenol conjugates were produced by grafting SPI individually with curcumin, naringenin, and catechin. The resulting conjugates showed better emulsifying properties and were used to develop active films containing rose essential oil. The effect of conjugation on the physicochemical and mechanical properties of these emulsion-based films was evaluated. The results showed that the barrier and mechanical properties of the films were improved when the SPI-polyphenol conjugates were used to emulsify the essential oil; in particular, the SPI-curcumin conjugate showed significant improvement. The improvements on the water vapor and oxygen barrier properties in the films were attributed to the formation of compact structure. Emulsion-based films stabilized by SPI-polyphenol conjugates showed antioxidant and antibacterial activities. They also demonstrated an ability to extend the shelf life of cherry tomatoes, as indicated by better preservation of weight, firmness, and ascorbic acid content.

Pickering nanoemulsion loaded with eugenol contributed to the improvement of konjac glucomannan film performance

Konjac glucomannan (KGM) is becoming a very potential food packaging material due to its good film-forming properties and stability. However, KGM film has several shortcomings such as low mechanical strength, strong water absorption, and poor self-antibacterial performance, which limits its application. Therefore, in order to enhance the mechanical and functional properties of KGM film, this study prepared Pickering nanoemulsion loaded with eugenol and added it to the KGM matrix to explore the improvement effect of Pickering nanoemulsion on KGM film properties. Compared to pure KGM film and eugenol directly added film, the mechanical strength of Pickering-KGM film was significantly improved due to the establishment of ample hydrogen bonding interactions between the β-cyclodextrin inclusion complex system and KGM. Pickering-KGM film had significant antioxidant capacity than pure KGM film and eugenol directly added KGM film (eugenol-KGM film) (~3.21 times better than KGM film, ~0.51 times better than eugenol-KGM film). In terms of antibacterial activity, Pickering-KGM film had good inhibitory effect on Escherichia coli, Staphylococcus aureus, and Candida albicans, and raspberry preservation experiment showed that the shelf life of the Pickering-KGM film could be extended to about 6 days. To sum up, this study developed a novel means to improve the film performance and provide a new insight for the development and application of food packaging film.

An investigation on the mechanical properties of a multi-layer film coated PMMA by nanoindentation

An investigation on the mechanical properties of a multi-layer film coated PMMA by nanoindentation

Development of Evaluation Methods and Equipment for Evaluating Mechanical Properties of Nano-coated Thin Films

Development of Evaluation Methods and Equipment for Evaluating Mechanical Properties of Nano-coated Thin Films

Amine functionalised graphene embedded polyvinyl alcohol (PVA) and PVA-chitosan hydrogel composites

A novel amine-functionalized graphene oxide (AFG) doped polyvinyl alcohol (PVA)/chitosan (PVA-Ch) composite film was developed using an eco-synthesis approach, eliminating the need for halogenated compounds. The resulting AFG-doped PVA/Chitosan (PVA-Ch/AFG) polymer film exhibited promising properties for controlled delivery and biosensing applications. The investigation included assessing the swelling behaviour, dissolution percent, gel fraction, and mechanical properties of the polymer film. The swelling characteristics of PVA-Ch and PVA-Ch/AFG were found to be pH and temperature-dependent across various pH ranges (3, 5, 7, and 9). Interestingly, PVA-Ch/AFG demonstrated a stable swelling pattern at pH 5 and 7, unaffected by changes in chitosan concentration, indicating enhanced stability compared to PVA-Ch. The study also explored the use of PVA-Ch/AFG in a drug delivery system, revealing controlled release of the model antibiotic amphicillin, emphasizing its potential in medical applications. Furthermore, the eco-friendly synthesis route underscored the safety of PVA-Ch/AFG for use in food and medical applications. Biocompatibility assessments, including biodegradability studies and cytotoxicity tests on fibroblasts (3T3 cells), confirmed the safety profile of PVA-Ch/AFG. In conclusion, the study suggests that PVA-Ch/AFG holds promise for bio-sensing applications, offering a flexible and colorimetric platform capable of encapsulating, adsorbing, and desorbing biomolecules such as drugs and sensing compounds.

A Study on the Preparation of a Vulcanizing Mixture and Its Application in Natural Rubber Latex.

The traditional preparation process of natural rubber latex requires tedious treatment of a variety of rubber additives. In this paper, a new process of wet mixed grinding was used to prepare a reinforced vulcanization mixture and a rapid vulcanization effect. The effect of different amounts of vulcanization mixtures on the mechanical properties of natural latex film was studied, and the pre-vulcanization process of latex and the vulcanization process of film were optimized. The results showed that with the increase in the amount of vulcanization mixture, the tensile strength increased from 5.96 MPa to 29.28 MPa, and the tear strength increased from 7.59 kN/m to 52.81 kN/m. When the vulcanization temperature of the latex film is heated from 80 °C to 100 °C, the vulcanization time is shortened by 5~6 times. The new vulcanization mixture prepared in this work has the characteristics of simple production and fast vulcanization speed, which provides a new solution for the development of the latex product industry.

Mechanical and barrier properties of chitosan-based composite film as food packaging: A review

Chitosan can serve as a natural alternative to petroleum-based components in food packaging; however, the mechanical and barrier properties of pure chitosan film possess certain limitations. This paper presents a comprehensive review on the mechanical and barrier properties of composite films formed by combining chitosan-based films with plasticizers, polysaccharides, proteins, and lipids. These composite films often exhibit superior mechanical strength and enhanced barrier performance compared to pure chitosan film, thereby expanding the potential applications of chitosan in food packaging. Chitosan represents an ideal raw material for developing innovative biofilms that can cater to diverse packaging requirements for various food products while offering promising prospects for broad application.

Bioinspired All‐Polyester Diblock Copolymers Made from Poly(Pentadecalactone) and Poly(3,4‐Ethylene Furanoate): Synthesis and Polymer Film Properties

AbstractBio‐based, fully degradable aliphatic‐aromatic block copolymers are synthesized from ω‐pentadecalatone and cyclic oligo(3,4‐ethylene furanoate). In the first approach, the ring‐opening polymerization of the cyclic oligo(3,4‐ethylene furanoate) is initiated by a poly(pentadecalactone) macroinitiator with a terminal hydroxy group. The reaction temperatures of the melt polymerization are 210–230 °C due to the high melting points of the oligo(3,4‐ethylene furanoate). Under these conditions, transesterification is observed. The blockiness of the reaction products depends on the reaction temperature and on the ratio of pentadecalactone to 3,4‐ethylene furanoate repeat units, which is 50:50, 80:20, and 90:10. At lower temperatures and more pentadecalactone content, the blockiness is larger. The number average molar mass of the block copolymers remains smaller than 20 000 g mol−1. In the second approach, poly(pentadecalactone) is functionalized with an alkyne group, and the OH group of the oligo(3,4‐ethylene furanoate) (molar mass 1900 g mol−1) is converted into an azide group. Connecting the two polymers in a copper‐catalyzed 1,3‐dipolar addition reaction (“click reaction”) yields block copolymers with a number average molar mass of 12 400 g mol−1. The mechanical properties of the polymer films are intermediate between those of the parent homopolymers.

Enhancing Mechanical Properties of Corn Bran Arabinoxylan Films for Sustainable Food Packaging.

Arabinoxylan (AX)-based films can improve the mechanical characteristics of biodegradable materials when utilized for food packaging. However, the mechanical properties of AX films for food packaging applications require thorough investigation to establish their viability. In this study, AX was extracted from corn bran coproducts of dry-milling (DCB), wet-milling (WCB), and dried distiller's grains with solubles (DDGS) using an acid-alkali method. Packaging materials were produced using these AX extracts, each combined with laccase and sorbitol, forming the basis for three different films. These films were then modified by immersing the surface in a lipase-acetate solution. We evaluated their mechanical characteristics, including thickness, tensile properties, tear resistance, and puncture resistance. The thickness and tensile properties of the modified AX films derived from DCB and DDGS showed significant improvements (p < 0.05) compared to the unmodified AX films. In contrast, the modified AX films from WCB showed no significant changes (p > 0.05) in thickness and tensile properties compared to the unmodified WCB AX films. A significant increase in tear resistance (p < 0.05) was observed in all modified AX films after immersion in the lipase-acetate mixture. While puncture resistance was enhanced in the modified AX films, the improvement was not statistically significant (p > 0.05) compared to the unmodified films. The presence of hydroxyl (OH) and carbonyl (CO) groups on the surfaces of AX films from DCB and DDGS, modified by the lipase-acetate solution, suggests excellent biodegradability properties. The modification process positively affected the AX films, rendering them more bendable, flexible, and resistant to deformation when stretched, compared to the unmodified AX films.

Investigation of physical, thermal, mechanical and gas permeability properties of low‐density polyethylene/ poly(4‐methyl‐1‐pentene) blend films and their utilization for fresh‐cut fruit and vegetable packaging applications

AbstractIn this study, low density polyethylene/poly(4‐methyl‐1‐pentene) (LDPE/PMP) blend films were prepared by melt compounding in a twin‐screw extruder then film casting in a single screw extruder equipped with a cast‐film. Morphological, thermal, and mechanical properties of flexible blend films were characterized by XRD, SEM, DSC analysis, and tensile tests. Solid‐state viscoelastic properties of samples were also quantified by measuring creep behaviors in DMA. Oxygen and carbon dioxide permeability values of films were measured. Their packaging film application performances were evaluated by observing the textural properties of fresh‐cut bananas stored into LDPE and a blend film bag and monitoring the ethylene, oxygen, carbon dioxide concentrations into the bags for 14 days. It was found that LDPE/PMP blends showed partially miscible structure but yielded highly transparent films. DSC results pointed out that the PMP significantly reduced the degree of crystallinity value of LDPE. On the other hand, PMP improved tensile strength and elastic modulus of LDPE. Creep tests indicated that the PMP addition significantly reduced the creep resistance and relaxation time of LDPE. This study clearly signified that the PMP dramatically increased the oxygen permeability value of LDPE. It has also been concluded that LDPE/PMP blend films can be used as a highly permeable packaging material for successfully extending the shelf life of fresh‐cut fruits and vegetables.Highlights LDPE/PMP films, despite being partially miscible, are highly transparent and made through melt compounding and film casting. Adding PMP to LDPE reduces crystallinity but improves tensile strength and elasticity, as shown by DSC tests. PMP reduces LDPE's creep resistance and quickens relaxation time, according to DMA creep tests. PMP greatly increases LDPE's oxygen permeability, ideal for gas‐transmitting packaging. LDPE/PMP film packaging prolongs the shelf life of fresh produce, proven in a banana storage study.

Fabrication of poly(acrylic acid)/chitosan/linseed mucilage films: Thermal and mechanical properties

AbstractThe use of biodegradable polymers in the plastics industry has been increasing in recent years. The study of the chemical, physical, thermal, and mechanical properties of films based on biodegradable components is of interest to technologists because these properties determine their applicability for food packaging. In this work, films based on natural polymers such as linseed mucilage (LM) and chitosan (CH), as well as poly(acrylic acid) (PAA) were obtained through the casting method and using V‐50 as the initiator. The films were characterized through Fourier Transform Infrared spectroscopy, and thermogravimetric analysis, and their water absorption and swelling capacity, and thermal and mechanical properties were determined. Homogenous flexible, translucid, amber‐colored films, with low absorption and solubility in water were obtained. It was demonstrated through Fourier Transform Infrared analysis the chemical interaction between C–H, CO, and C–O chemical groups of LM, CH, and PAA. In addition, films showed high resistance to thermal decomposition between 125 and 425°C. The mechanical tests of tension allowed the composition of LM in the film, the behavior variates between a plastic and/or elastic material and with tensile strength (Rm) values between 10.8 and 16.4 MPa and elastic modulus (E) values between 56.2 and 169.2 GPa, we observed that at higher quantities of LM and thickness, both E and Rm tend to increase, while %EL decreases. This led us to conclude that the material transitioned from ductile and malleable to rigid and brittle. The films obtained with different ratios of LM/CH/PAA may exhibit a semi‐interpenetrating polymeric networking type morphology.Highlights Thermal and mechanical properties are of interest in food packaging materials. Water absorption can impact the packaged food. Films can be processed on existing machines for conventional plastics. Some conventional plastics could be replaced by these biodegradable films. Biodegradable films are of great interest to the industry of food packaging.

Development of Antifungal Packaging From Low‐Density Polyethylene With Essential Oil of Oregano and Potassium Sorbate

ABSTRACTAntimicrobial low‐density polyethylene (LDPE) films were developed by adding 0%, 0.5%, 1.0%, 2.5% and 5.0% (w/w) of Mexican oregano essential oil (OEO) or potassium sorbate (PS) as a positive antifungal control to inhibit the growth of Penicillium expansum, Penicillium citrinum and Aspergillus niger in vitro. Three methods of adding OEO in LDPE were evaluated; the best OEO yield in film was achieved when OEO was incorporated after laminating (88%); otherwise, when added into cool‐melting resin, OEO lost up to 91.5% from LDPE and completely volatilized (&gt;99%) when combined with the resin before melting. PS yields in LDPE film were &gt; 88% when incorporated into cool‐melted resin. Antimicrobial films with 2.5% or 5.0% (w/w) OEO or PS delayed the growth of P. expansum and P. citrinum for up to 4–5 days, and for A. niger, only films with 5.0% of OEO retarded its growth for 5 days. The modified Gompertz model was used to describe mould growth response, obtaining the parameters A (maximum growth), μm (maximum growth rate) and λ (lag phase), which correctly fit the data. P. citrinum was the most sensitive mould, and A. niger was the most resistant to the tested antimicrobials. The addition of antimicrobial agents significantly (p &lt; 0.05) impacted the physical and mechanical properties of the LDPE films, wherein thickness and puncture strength were increased, and the colour changed (reducing the transparency and promoting the yellowness). In contrast, the water vapour transmission rate was dropped only by incorporating PS.

Nitrogen-Doped Diamond-like Carbon Buffer Layer Enhances the Mechanical and Tribological Properties of Diamond-like Carbon Films Deposited on Nitrile Rubber Substrate

The poor adhesion between the DLC film and rubber restricts its application of seals. Introducing a suitable interlayer can bolster the adhesion of the coating or film. In this study, nitrogen-doped diamond-like carbon (N-DLC) emerged as the optimal intermediate layer between rubber and DLC. A series of N-DLC/DLC multilayer films were fabricated via DC magnetron sputtering on nitrile rubber (NBR) substrates, varying the substrate bias voltage (0 V, 100 V, 200 V). A scanning electron microscopy analysis revealed that the composite film surface was smoother than the DLC film alone. The results of Raman spectroscopy and X-ray photoelectron spectroscopy indicated a robust bond between nitrogen and carbon atoms in the composite film, with nitrogen facilitating the conversion of sp3C-C bonds into sp2C=C. Mechanical tests demonstrated that the N-DLC interlayer improved film adhesion and reduced the CoF of the composite film to 0.2–0.3. Specifically, the CoF of the N-DLC/DLC film prepared at 100 V was as low as 0.20, with a wear amount of 1.13 mg. Consequently, the inclusion of the N-DLC interlayer substantially enhanced the mechanical and tribological properties of DLC-coated NBR, rendering this coating highly advantageous for various applications.

Microstructure and mechanical properties of Cr films with different orientations before and after plasma nitriding

Microstructure and mechanical properties of Cr films with different orientations before and after plasma nitriding

Synthesis and self-assembly of bottlebrush block copolymer electrolytes for solid-state supercapacitors

All-solid-state supercapacitors have attracted increasing attention in recent decades owing to rapid advancements in safe, flexible, and wearable energy storage devices. This study demonstrates a bottlebrush block copolymer electrolyte consisting of poly(styrene-b-butadiene-b-styrene)-g-poly(ethylene glycol) behenyl ether methacrylate (SBS-g-PEGBEM) (simply SgP) for all-solid-state supercapacitors. Due to the adhesive nature and robust mechanical properties of SgP film, devices can be manufactured without the need for separators or packaging. The nonpolar SBS domains serve as scaffolds within the polymer matrix, while the polar PEGBEM domains offer interactive sites for polar ionic liquids (ILs). The synergy between precisely defined nanostructures and the subsequent well-dissociated ions enhances efficient ion transport through the ionic channels. As a result, the supercapacitor with SgP/IL electrolyte exhibits remarkable electrochemical performance. This includes a wide potential window of 2.4 V, an ionic conductivity of 2.4 mS cm−1, and maximum energy density and power density of 28.1 Wh kg−1 and 3080 W kg−1, respectively. The supercapacitor also demonstrates high cycle stability with 87.7 % capacitance retention after 5,000 cycles. The positive impact of the PEGBEM side chains is investigated via molecular dynamics simulations. Thus, this study presents a novel strategy for solid-state electrolytes, offering potential advancements in next-generation energy storage devices.

Manufacturing process and annealing influence on the dynamic mechanical properties and physical structure of LLDPE thin films

Thin films of Linear Low-Density Polyethylene are used for stratospheric balloon applications. They undergo tensile mechanical stress on a wide range of temperatures [-95; 55]°C. The aim of this study is to compare the influence of blown film and double-bubble manufacturing processes on the crystalline phase and mechanical properties of the films through their operating temperatures (flight, storage, and transportation temperatures). Dynamic Mechanical Analysis and Differential Scanning Calorimetry have been used to monitor the dynamic mechanical properties in tension mode and the crystalline phase of the films respectively. The films mechanical properties are dependent on their manufacturing process. The double-bubble process allows isotropic tensile mechanical properties regarding stretching direction, whereas the blown film process favors only transversal direction. To simulate different storage conditions, annealing has been performed. The influence of annealing on the tensile mechanical properties of the films depends mainly on the internal stress stored during manufacturing. The double-bubble process produces a biaxially stretched film with a higher stretching ratio than blown films. The dissipated internal stress can be associated with thermal shrinkage and goes up to 10 % for the biaxially stretched film. The more internal stress is stored, the more E′ and E″ increases. Annealing also favors the formation of a secondary crystalline phase that is dependent on annealing temperature and time, and exhibits αc relaxation. After annealing, the amorphous phase is less stretched, and the crystalline phase keeps its orientation.

Influence of DMSO Non-Toxic Solvent on the Mechanical and Chemical Properties of a PVDF Thin Film

Influence of DMSO Non-Toxic Solvent on the Mechanical and Chemical Properties of a PVDF Thin Film

Influence of Different Polymorphs on the Electrical and Mechanical Properties of F4TCNQ-Doped Regioregular P3BT Films

Influence of Different Polymorphs on the Electrical and Mechanical Properties of F4TCNQ-Doped Regioregular P3BT Films