Search Results (149)

Circularly polarized luminescence (CPL) materials have shown great application potential in the fields of three-dimensional displays, bioimaging, and information encryption and decryption. The chirality enhancement of CPL by a physical chiral environment, involving the delivery of structural asymmetry from helical architectures to luminescent molecules through electromagnetic field resonance, represents an innovative approach for constructing high-performance CPL materials. Liquid crystal polymers (LCPs), possessing helical superstructures, show great potential in constructing CPL systems. By modulating the chirality transfer from the helical structural environment of LCPs to luminescent sources via distinct strategies, the CPL properties of LCP-based composites are readily generated and tailored. This review summarizes the newest construction strategies of LCP-based CPL materials and provides a perspective on their emerging applications and future opportunities. This review can deepen our understanding of the fundamentals of chirality transfer and shed light on the development of functional chiral luminescent materials. Full article

This study investigated the effects of curdlan (CUR) with different helical conformations on the gelling behavior and mechanisms of heat-induced soy protein isolate (SPI) gels. The results demonstrated that CUR significantly improved the functional properties of SPI gels, including water-holding capacity (0.31–5.06% increase), gel strength (7.01–240.51% enhancement), textural properties, viscoelasticity, and thermal stability. The incorporation of CUR facilitated the unfolding and cross-linking of SPI molecules, leading to enhanced network formation. Notably, SPI composite gels containing CUR with an ordered triple-helix bundled structure exhibited superior gelling performance compared to other helical conformations, characterized by a more compact and uniform microstructure. This improvement was attributed to stronger hydrogen bonding interactions between the triple-helix CUR and SPI molecules. Furthermore, the entanglement of triple-helix CUR with SPI promoted the formation of a denser and more homogeneous interpenetrating polymer network. These findings indicate that triple-helix CUR is highly effective in optimizing the gelling characteristics of heat-induced SPI gels. This study provides new insights into the structure–function relationship of CUR in SPI-based gel systems, offering potential strategies for designing high-performance protein–polysaccharide composite gels. The findings establish a theoretical foundation for applications in the food industry. Full article

This study proposes a bionic helical configuration design concept, focusing on glass-fiber-reinforced polymer matrix composites. Through a combination of experimental and numerical simulation methods, it systematically investigates the resistance to multiple impacts and damage tolerance. The research designs and fabricates two types of bionic laminates: a cross-helical and a symmetric-helical structures. By conducting repeated impact experiments at 5 J of energy for 1, 5, 10, and 15 impact times and employing advanced characterization techniques, such as ultrasonic C-scan and X-ray CT, the study reveals the mechanisms of interlaminar damage propagation and failure characteristics. Based on experimental findings, a finite element model encompassing the entire impact process and post-impact compression behavior is established. Utilizing this model, three optimized novel bionic configurations are further developed, providing new insights and theoretical support for the structural design of high-performance impact-resistant polymer matrix composites. Full article

Helical ladder polymers attract attention because of their well-defined, one-handed helical ladder structures and unique properties, which differ from precursor polymers that have random-coil conformations. However, the synthesis of helical ladder polymers is difficult and inhibits their functions and applications. In this study, we reported the synthesis of amphiphilic optically active 2,2′-tethered binaphthyl-embedded helical ladder polymers carrying hydrophilic oligo (ethylene glycol) (OEG) as side chains through quantitative and chemoselective acid-promoted intramolecular cyclization of random-coil precursor polymers. The obtained helical ladder polymers exhibited dramatic circular dichroism (CD) and circularly polarized luminescence (CPL) enhancement. Moreover, we further established a circularly polarized fluorescence-energy transfer (CPF-ET) strategy in which the helical ladder polymers work as a donor, emitting circularly polarized fluorescence to excite an achiral fluorophore (coumarin-6) as the acceptor, producing green CPL with luminescence dissymmetry factor (2.5 × 10⁻⁴). Full article

In this work is investigated the bond behavior of FRP bars considering basalt as a fiber and also cases where graphene is introduced as a polymer filler. Standard FRP bars where glass is used as fiber is tested under the same conditions in order to have a benchmark. Three different temperatures are considered in the tests, including room temperature and a temperature higher than the glass transition of the polymer. At room temperature the effect of concrete strength and the bar diameter on bond is also investigated. The study developed is experimental, through pull-out tests, as well as numerical, through simulations by the Finite Element method. Cases where basalt fibers are associated to helically-wounded surface treatment showed at least 41.7% superior bond behavior among all cases considered with this fiber at room temperature. Studies with graphene were exploratory and limited to only one percentage of addition. However, results suggest that the addition is able to improve behavior of the polyester resin of the matrix at room temperatures by 49% and at higher temperatures bond degradation was 44% smaller when compared with the literature. It was not observed a statistically significant influence of the concrete strength on bond. Diameter influence on bond was mostly linked to surface treatment. Full article

Springs are widely used in industries such as aerospace and automotive. As the demand for emission reduction grows, the research on lightweight spring performance is becoming increasingly important. This study analyses the mechanical performance of triple-layer braided composite helical springs (TCHS) under various loads and compression angles. Firstly, the optimal high-temperature curing condition of the epoxy resin was determined through tensile and three-point bending analysis. Then, TCHS were fabricated based on optimal epoxy curing conditions, and multi-angle compression tests under different loads were carried out. Simultaneously, strain gauges were installed at various positions and orientations on the inner and outer sides of the spring wire to reveal strain patterns during the compression. The test results indicate that stiffness decreases with increasing compression angle. Additionally, the strain in the inner and outer positions in different directions of the same region increased with the rise in compression force and angle, and strains in the helical direction were the largest. Subsequently, strain in the helical direction across different regions further showed that maximum strain occurred in the centre coil (region 2), with inner and outer helical direction strains reaching −5116.89 με and 5700.15 με, respectively, which are 71.3% and 90.4% higher than those in region 1 and 73.2% and 92.9% higher than those in region 3. As the compression load increased, cracks appeared on the outer side of the centre coil. In addition, the crack was perpendicular to the helical direction, further confirming that the highest strain occurred in the helical direction. This study provides an in-depth analysis of the impact of angle-specific loads on TCHS, offering valuable insights for the design and optimisation of composite helical springs and laying a theoretical foundation for their future development. Full article

The formation of self-crosslinking chitosan hydrogels using carboxylic acids has a number of limitations. Chitosan dissolves in oxalic, malonic, and succinic acids at a ratio of 1 amino group to 2 carboxyl groups into viscous solutions (G′ < G′′), but does not dissolve with lower amounts of the acid. Mixing chitosan hydrochloride with disodium carboxylates does not afford gels, but only a coacervate in the case of disodium oxalate, which dissolves upon dialysis. In the homologous series of N-carboxyalkyl derivatives (alkyl = methyl, ethyl, propyl), all members form gels (G′ > G′′). At approx. 50% of substitution, the storage modulus increases from 40 Pa (methyl) to 30,000 Pa (propyl) indicating the increasing strength of intermolecular interactions with the increasing length of the alkyl spacer. This could indicate that a sufficiently long spacer is required to properly connect the chitosan helices. N-succinyl chitosan, where the spacer is attached to the backbone as an amide, also forms polymer gels across all degrees of N-acylation. When compared to N-carboxypropyl chitosan, the latter forms significantly stiffer gels that swell less. This indicates that one covalent bond, a sufficient length, and the conformational flexibility of the spacer are important for gelation. Full article

The eccentric rotor extruder (ERE) is polymer processing equipment that exhibits excellent processing capabilities for materials with extremely high viscosity, which are difficult to plastically deform and transport efficiently. However, the mass transfer mechanism in the solid conveying section of this new device is fundamentally different from that of traditional extruders, and no related research has been reported. This study uses discrete element method (DEM) simulation technology to model the solid conveying process of the ERE. By visualizing the positive displacement conveying process, and with an analysis of the output parameters, the study clarifies the mass transfer principles and quantifies the conveying capacity, providing guidance for optimizing the extruder design. The simulation results show that the ERE exhibits positive displacement conveying characteristics, with the conveying process achieved by the forward movement of the cavities (closed cavities between the rotor and stator) in a helical manner. However, differences in the dual-cavity (two types of cavities) feeding process and low fill level can lead to significant fluctuations in extrusion output and reduced conveying capacity. To address these issues, an improvement scheme for the dual-cavity feed opening is proposed, with feed openings designed with different opening lengths. Then, by analyzing the particle coordinate data from the simulation output, the conveying capacities of different feed opening structures are quantified and optimized. Finally, experimental and simulation verification results indicate that the optimized structure significantly improves the issues of uneven filling and low fill level, with good correspondence between the simulation and experimental results. Simulation results show that, compared with the original structure, the optimized dual-feed opening structure increases the feed capacity from 3953 particles per cavity to 5132 particles per cavity, an improvement of 29.8%, and it achieves balanced filling between the two cavities. Experimental validation indicates that the UPE4040 output can be increased from 165.3 g/min with structure op-00 to 231.7 g/min with the optimized structure op-05. Full article

The optical sensing of chirality is widely used in many fields, such as pharmaceuticals, agriculture, food, and environmental materials. In this context, the color-based cascade amplification of chirality, coupled with chiral recognition for analytes, provides a low-cost and straightforward detection method that avoids the use of expensive and sophisticated instrumentation. However, the realization of chiral detection using this approach is still challenging because the construction of a three-dimensional optical recognition site is required to easily discern differences in chirality. Therefore, considerable efforts have been dedicated to developing a hierarchical approach based on molecular organization to provide colorimetric sensors for chirality detection. This review covers function-integrated molecular sensors with colorimetric responsive sites based on absorption, fluorescence, and aggregation-induced emission enabled by molecular organization. In line with the hierarchical approach, data-driven chemometrics is a useful method for quantitative and accurate chiral pattern recognition. Finally, colorimetric nanomaterials are discussed, focusing on sensing platforms using noble-metal nanoparticles, carbon dots, and photonic crystal gels. Full article

The sustainable production of carbon-free fuels such as hydrogen is an important goal in the search for alternative energy sources. Herein, we report a peptide-based system for light-driven hydrogen evolution from water under neutral conditions. The M1 peptide is an ABC triblock polymer featuring two coiled-coil alpha-helical regions flanking a water-soluble, polyanionic, intrinsically disordered region. M1 formed a hydrogel at high concentrations upon binding to cobalt protoporphyrin IX. This process is driven by the terminal regions, which coordinate the metalloporphyrin through histidine residues and form helical oligomers interconnected by flexible, intrinsically disordered regions, resulting in network formation. Co-M1 catalyzes hydrogen production upon irradiation in the presence of a photosensitizer and a sacrificial electron donor; the activity of Co-M1 is eight times higher than that of free Co-PPIX. Full article

Seeking a supramolecular chiral system induced by trace chiral molecules instead of traditional complex and expensive chiral ligands to achieve high yield or ee value conversion of the products is of great significance in asymmetric synthesis but still remains a challenge. Herein, two types of double helical supramolecular chiral systems, (M)-Helix and (P)-Helix, with opposite chiral optics were constructed in situ using tyrosine-functionalized pillar[5]arene as inducers. These systems exhibit chiroptical stability and enable remarkable chirality amplification from 7 mol% chiral seeds. When applied to intermolecular olefin cyano-trifluoromethylation, (M)-Helix exhibits remarkable catalytic efficiency (yield up to 89%), whereas (P)-Helix achieves higher enantioselectivity (ee up to 84%). This research will provide new ideas for supramolecular chiral catalysts in organic asymmetric catalysis applications. Full article

The atomic structure, electronic, phonon, and optical properties of chalcogen helical chains (S, Se, Te) were studied using line symmetry groups and DFT calculations. The whole possible range of torsion deformations (from 0° to 180°), as well as the range of axial deformations (from 0.6 to 1.6) were considered. For the studied chains, the atomic and electronic structures at the energy minima were found. It was shown that for the considered chalcogen chains, the minimum of electronic energy is in the region of rotation angles ~103–107°. The electronic structure of all chains was considered in the helical Brillouin zone, which made it possible to trace its evolution up to the extreme torsional deformations: 0° (linear chain) and 180° (zigzag chain). A method for obtaining the dispersion of phonon states in the helical Brillouin zone has been developed based on the results of calculations by the CRYSTAL17 program. This allowed us to trace the evolution of phonon dispersion curves under torsion deformations up to their extreme values. Based on the known selection rules for helical polymers, the energies of optical, IR, and Raman transitions were obtained. This allows one to predict the optical properties of atomic chalcogen chains—both in a free state and inside carbon nanotubes. Full article

Helical carbon nanotubes (HCNTs) with different geometrical properties were constructed and incorporated into nanocomposites for the investigation of the anti-crack mechanism. The interfacial mechanical properties of the nanocomposites reinforced with straight carbon nanotubes and various types of HCNTs were investigated through the pullout of HCNTs in the crack propagation using molecular dynamics (MD). The results show that the pullout force of HCNTs is much higher than that of CNTs because the physical interlock between HCNTs and matrices is much stronger than the van der Waals (vdW) interactions between CNTs and matrices. Remarkably, HCNTs with a large pitch length can not only effectively prevent the initiation of breakages but also hinder the growth of cracks, while HCNTs with a small diameter and tube radius cannot even effectively prevent the initiation of cracks, which is similar to straight CNTs. Moreover, the shear resistance of HCNTs increases with the increase in the helix angle, which remains at a high level when the helix angle reaches the critical value. However, HCNTs with a small helix angle and large diameter can carry out more polymer chains, while snake-like HCNTs and HCNTs with a small diameter and helix angle can hardly carry out any polymer chain during the pullout process and show similar interfacial properties to the straight CNTs. Full article

Recent developments in the synthesis of substituted polyacetylenes have considerably benefitted from advancements in organometallic catalysis; however, most important developments rely on the advent of Rh-catalyzed living polymerizations. The latter not only allow the tailoring of well-defined degrees of polymerization with low and narrow polydispersity but also enable access to stereochemical well-defined cis-transoidal polymers with a helical structure. These novel polymers open new avenues for application in photonics and electronics. Rh-catalyzed living polymerizations are mild and concise metal-catalyzed polymer syntheses that not only allow for the decoration of sidechains with multiple functionalities, including chiral units, but also enable enantioselective induction of helical chirality, memory of chirality, well-defined copolymerization, and end-group functionalization at both termini. This review summarizes recent developments in metal-catalyzed syntheses of substituted polyacetylenes, with a special focus on Rh-catalyzed living polymerizations. Full article

Biocompatible materials fabricated from natural protein polymers are an attractive alternative to conventional petroleum-based plastics. They offer a green, sustainable fabrication method while also opening new applications in biomedical sciences. Available from several sources in the wild and on domestic farms, silk is a widely used biopolymer and one of the strongest natural materials. This study aims to compare five different types of silk (Mori, Thai, Muga, Tussah, and Eri) fabricated into thin composite films in conjunction with plant-based proteins. To offer a wider range of morphologies, corn zein, another widely available protein material, was introduced into the silk protein networks to form blended polymers with various ratios of silk to zein. This resulted in the successful alloying of protein from an animal source with protein from a plant source. The material properties were confirmed through structural, morphological, and thermal analyses. FTIR analysis revealed the dominance of intramolecular beta-sheet structures in wild silks, while the domestic silks and zein favored random coil and alpha-helical structures, respectively. Post-treatments using water annealing further refined the structure and morphology of the films, resulting in stable composites with both inter- and intramolecular beta-sheet structures in wild silks. While in domestic silks, the random coils were converted into intermolecular beta-sheets with enhanced beta-sheet crystallinity. This improvement significantly enhanced the thermal and structural properties of the materials. By deciding on the source, ratio, and treatment of these biopolymers, it is possible to tailor protein blends for a wide range of applications in medicine, tissue engineering, food packaging, drug delivery, and bio-optics. Full article