Functional Polymeric Materials Research Articles

Effect of lignin on the structure-property behavior of metal-coordinated and chemically crosslinked ethylene-propylene-diene-monomer composites

The efficient development and utilization of green biomass-based macromolecule engineering materials are essential for the sustainable development of human civilization. In this study, lignin-based ethylene-propylene-diene-monomer (EPDM) composites with excellent mechanical performance were fabricated using a simple method. The effects of water-insoluble enzymatically hydrolyzed lignin (EL) and alkali lignin (KL) on the mechanical performance of the composites were investigated separately. The results showed that the tensile strength of EPDM reinforced with KL and EL increased to 24.5 MPa and 22.1 MPa, respectively, surpassing that of the carbon black (CB)-reinforced EPDM. After 72 h of thermo-oxidative aging, the retention rates of the tensile strength and elongation at break in the lignin-reinforced EPDM were much better than those formed with pure CB, indicating that lignin significantly improved the thermo-oxidative aging resistance of the composites. In summary, the Zn2+ coordination bonds formed between the interface of EPDM and lignin in lignin/CB/EPDM ternary composites effectively improved the mechanical performance and aging resistance of the composites. This study has significant implications for enhancing the utilization of lignin and green functional polymer materials.

O/SExchange Reaction in Synthesizing Sulfur-Containing Polymers.

Using carbon disulfide (CS2) and carbonyl sulfide (COS) as sulfur-containing and one-carbon feedstocks to make value-added products is paramount for both pure and applied chemistry and environmental science. One of the practical strategies is to copolymerize these bulk chemicals with epoxides to produce sulfur-containing polymers. This approach contributes to improving the sustainability of polymer manufacturing, provides highly desired functional polymer materials, and has attracted much attention. However, these copolymerizations invariably exhibit the intensely complicated chemistry of O/S exchange reaction, leading to sulfur-containing polymers with diverse architectures. As the understanding of O/S exchange continues to deepen, recent efforts have guided significant advances in the synthesis of CS2- and COS-based polymers. This review examines the O/S exchange chemistry and summarizes the recent progress in this field to promote the further advance of synthesizing sulfur-containing polymers from CS2 and COS.

Green conversion of carbon disulfide to degradable polydithiourethanes through catalyst-free multicomponent polymerizations of diamines, carbon disulfide and diacrylates

In the pursuit of advanced functional polymer materials, sulfur-containing polymers have received tremendous attention owing to their superior chemical stability, high refractive indices, various supramolecular interactions, and robust dynamic covalent chemistry. However, their synthesis usually involves either expensive monomers or toxic byproducts and requires catalysts, thus hindering their widespread application. In this work, we present a catalyst-free multicomponent polymerization in organic solvents for the synthesis of various polydithiourethanes with excellent yields (up to 98 %) and high molecular weights (up to 112 kg/mol). This reaction involves the direct polymerization of carbon disulfide, an abundant one-carbon feedstock, with commercially available diamines and diacrylates. This polyaddition process demonstrates high atom economy and no byproduct, occurring at room temperature without the need for a catalyst, thus exhibiting excellent green chemistry metrics. By utilizing the dynamic covalent chemistry of dithiourethane groups, these polymers can be efficiently degraded via aminolysis and used to fabricate reprocessable vitrimers. This multicomponent polymerization opens up a new avenue for the efficient utilization of carbon disulfide resources and accelerates the exploration of diversified sulfur-containing functional polymer materials.

Multicomponent Polymerizations of Elemental Sulfur, CH2Cl2, and Aromatic Amines toward Chemically Recyclable Functional Aromatic Polythioureas.

The exploration of new polymer materials required the development of efficient, economic, robust, and scalable synthetic routes, taking energy consumption, environmental benefit, and sustainability into overall consideration. Herein, through retro-polymerization analysis of functional aromatic polythioureas, a multicomponent reaction of elemental sulfur, CH2Cl2, and aromatic amines was designed with the assistance of fluoride, and efficient, economic, and robust multicomponent polymerizations (MCPs) of these three abundantly available cheap monomers, elemental sulfur, CH2Cl2, and aromatic diamines, were developed to realize scalable conversion directly from sulfur to a series of functional aromatic polythioureas with high molecular weights (Mn up to 50,800 g/mol) in excellent yields (up to 98%). The synergistic cooperation of the strong and selective coordination of thiourea with gold ions and the redox property of aromatic polythiourea enable in situ reduction of Au3+ to elemental gold under a normal bench condition. Furthermore, the functional aromatic polythiourea could be chemically recycled through aminolysis with NH3·H2O to afford a diamine monomer in 83% isolated yield. The development of elemental sulfur-based MCP has brought the opportunity to access cost-effective and sustainable sulfur-containing functional polymer materials, which is anticipated to provide a solution for the utilization of sulfur waste and making profitable polymer materials.

Application of pfg NMR diffusometry to study diffusion and ionization phenomena in plasticized polymeric membranes doped with ionic liquids

Ionic liquids (ILs) are increasingly used as promising organic solvents for a variety of applications, including electrochemical processes, novel separation techniques and innovative methods of synthesis, due to their low volatility, excellent solvation properties, high ionic conductivity and electrochemical stability. Moreover, the tunable properties of ILs determined by their composition make them favorable candidates as dopants for composite and/or functional polymeric materials, e.g. in the membranes of chemical sensors. To effectively use ILs in polymeric materials and control the characteristics of the latter, one should develop a complete understanding of the properties of ILs in the polymeric phase, such as their diffusion and ionic behavior.In our previous work, we applied pulsed field gradient (PFG) NMR technique to verify the results of a chronopotentiometric method conventionally used to determine the diffusion coefficients and electrolytic properties of electrolytes in plasticized poly(vinyl chloride) (PVC) membranes of chemical sensors. The results obtained with these two independent methods were in good agreement, confirming that PEG NMR diffusometry is a viable technique for assessing the diffusion properties of species even in highly viscous polymeric media of low polarity.Here we report a comprehensive study of the transport and ionic behavior of IL 1-hexyl-3-methyl-1H-imidazolium bis[(trifluoromethyl)sulfonyl]amide ([C6Meim][NTf2]) in a poly(vinyl chloride) matrix, performed in situ by means of PFG NMR diffusometry. A number of sets of spectra for the 1H and 19F nuclei of the [C6Meim][NTf2] ionic liquid in PVC membranes doped with the plasticizer bis(2-ethylhexyl)sebacate were registered at different amplitudes of the magnetic field gradient. The mobility of both individual ions of the IL and the formed ion associates was investigated over a broad range of IL concentrations in the PVC matrix; in addition, the ionization degree and dissociation constant of [C6Meim][NTf2] were determined and their dependence on the IL content was traced.

Thermophysical and adhesive properties of functional polymer materials based on epoxy resin and silicon-containing component

The work was aimed at developing an adhesive formulation with increased adhesive strength for metals. It contains an epoxy resin of the bisphenol type СHS-TROXY 520 (an analogue of ED-20), an amine hardener triethanolamine (TEA) and a silicon-containing component (3-isocyanatopropyl)triethoxysilane, designated as NCO-Si, with an optimal ratio of components. The content of NCO-Si in the formulations was 0.5, 1.0, 3.0 and 5.0 wt. %, respectively. The gradual transformation of the epoxy system into a three-dimensional network with the formation of ester and urethane groups was shown by IR spectroscopy method. Tensile and shear strength were determined using the tearing machine R-50 in accordance with current standards. It was found that the maximum values of physical and mechanical parameters were obtained when the amount of NCO-Si was 3 wt. %. The maximum values of adhesion strength to steel substrates δst. = 58.5 MPa significantly exceed those for neat epoxy formulations. The shear strength values for steel plates τst. = 21 MPa increase by 60 %, for aluminium plates they are δAl =14.5 MPa and increase by 48 %. The morphology of the samples has been studied by means of optical microscopy. It is shown that the modified NCO-Si samples are characterised by a phase-separated structure. At a minimum amount of NCO-Si (0.5 wt. %), structurally disordered spherical domains with a size of ~1÷3 μm are observed, an increase in the content of the organosilicon component leads to the formation of interconnected regular structures, which are less pronounced at 1.0 wt. % of NCO-Si and clear at 3.0 and 5.0 wt. % of NCO-Si. Thermogravimetric analysis (TGA) was performed as well. It is shown that the modification of epoxy resin by a silicon-containing component with NCO-Si groups leads to an improvement in thermophysical parameters, a decrease in internal stresses and the formation of a material with a structure close to equilibrium.

Nanocellulose as an Ecofriendly Source in Nanoscience: Synthesis, Characterization, Properties, and Applications—A Review

AbstractNanocellulose is a promising future material which has got attention due to its unique characteristics. Properties which make nanocellulose special are the eco‐friendliness, high strength, stiffness, renewability, abundance, tunable surface characteristics, and low weight. This review addresses major factors like processing of nanocellulose, modification, properties, preparation of nanocomposites from nanocellulose, and their application in different fields. This review facilitates the selection of biomass sources, processing techniques for NC synthesis, application, and challenges. This review also emphasizes on different applications of nanocellulose reinforced polymer composites in different areas such as biomedical, packaging, electronic and environmental remediation, etc. Recent developments in the processing of cellulose nanocomposites using solution casting and other complex methods have been highlighted. As an emerging functional polymeric material, nanocellulose has become a research hotspot. The importance of nanocellulose in future includes the design of nanocellulose as per the specific user requirements, reduction of the production cost, and making customized products using nanocellulose using green processing. Hence this review is intended to provide new insights into the field of eco‐friendly fundamental materials with in‐depth perspectives and current research trends in its future applications.

Bioinspired superhydrophobic surfaces with silver and nitric oxide-releasing capabilities to prevent device-associated infections and thrombosis

Bacteria-associated infections and thrombus formation are the two major complications plaguing the application of blood-contacting medical devices. Therefore, functionalized surfaces and drug delivery for passive and active antifouling strategies have been employed. Herein, we report the novel integration of bio-inspired superhydrophobicity with nitric oxide release to obtain a functional polymeric material with anti-thrombogenic and antimicrobial characteristics. The nitric oxide release acts as an antimicrobial agent and platelet inhibitor, while the superhydrophobic components prevent non-specific biofouling. Widely used medical-grade silicone rubber (SR) substrates that are known to be susceptible to biofilm and thrombus formation were dip-coated with fluorinated silicon dioxide (SiO2) and silver (Ag) nanoparticles (NPs) using an adhesive polymer as a binder. Thereafter, the resulting superhydrophobic (SH) SR substrates were impregnated with S-nitroso-N-acetylpenicillamine (SNAP, an NO donor) to obtain a superhydrophobic, Ag-bound, NO-releasing (SH-SiAgNO) surface. The SH-SiAgNO surfaces had the lowest amount of viable adhered E. coli (> 99.9 % reduction), S. aureus (> 99.8 % reduction), and platelets (> 96.1 % reduction) as compared to controls while demonstrating no cytotoxic effects on fibroblast cells. Thus, this innovative approach is the first to combine SNAP with an antifouling SH polymer surface that possesses the immense potential to minimize medical device-associated complications without using conventional systemic anticoagulation and antibiotic treatments.

Functionalization of sterculia gum for making platform hydrogels via network formation for use in drug delivery

Recently, various advancements have been made in the development of functional polymeric materials for innovative applications. Herein this work, functionalization of sterculia gum (SG) was carried out via grafting of poly(2-(methacryloyloxy) ethyltrimethylammonium chloride) (METAC)-polyvinyl pyrrolidone (PVP) to develop hydrogel dressings as a platform for use in drug delivery (DD). The innovation of the present work is the exploration of inherent antioxidant and antimicrobial properties of the SG along with antimicrobial characteristic of poly(METAC) and PVP, to design the doxycycline encapsulated hydrogel dressings for better wound healing. FESEM, EDS and AFM analyzed the surface morphology of hydrogels. FTIR, 13C NMR and XRD inferred inclusion of poly(METAC)-PVP into polymers. 13C NMR confirmed the incorporation of poly(METAC) and PVP onto gum by the presence of a peak at 54.74 ppm because of methyl carbon attached to quaternary nitrogen of poly(METAC) and at 45.48 ppm due to the ring carbon of PVP along with FTIR peak at 949 cm−1 because of CN bending of quaternary nitrogen of poy (METAC). Thermal characterization of copolymers has been performed using TGA analysis. One gram of copolymeric hydrogel dressing absorbed 6.51 ± 0.03 g simulated salivary fluid (SSF) and 7.65 ± 0.03 g simulated wound fluid (SWF). Release of doxycycline drug occurred in a sustained manner and followed the Non-Fickian diffusion mechanism from hydrogels. The release profile was most effectively described by Hixon-Crowell kinetic model. Hydrogel demonstrated biocompatibility and expressed thrombogenicity 79.7 ± 4.9 % during its polymer-blood interactions. Copolymer revealed mucoadhesive property, requiring a force of 77.00 ± 0.01 mN to detach from bio-membrane. Additionally, it exhibited antioxidant features, showing 43.81 ± 0.286 % free radical scavenging. Hydrogel dressings were mechanically stable and revealed 0.76 ± 0.09 N mm−2 tensile strength and 9.18 ± 0.01 N burst strength. Polymer films were permeable to oxygen and water vapor and were impermeable to microorganisms. Hydrogel dressings exhibited antimicrobial properties against Pseudomonas aeruginosa and Staphylococcus aureus bacteria. Overall, these properties displayed the suitability of hydrogels for wound dressing (WD) applications which may actively enhance wound healing.

Exploring the potential applications of amphiphilic carbon dots based nanocomposite hydrogel in liquid chromatographic separations

BackgroundDue to their excellent stability, low toxicity, flexible modification and adjustable functionality, carbon dots (CDs) have a promising application prospect in the field of chromatographic stationary phases. Hydrogels are new functional polymer materials with three-dimensional network structure that have excellent hydrophilicity, high porosity and unique mechanical properties, which are also good candidate materials for liquid chromatography. Nevertheless, a review of the literature reveals that CDs based nanocomposite hydrogels have not yet been reported as HPLC stationary phases. ResultsIn this work, amphiphilic CDs with multiple functional groups and polyacrylic acid hydrogel were grafted to the surface of silica gel by an in-situ polymerization method, and a CDs/polyacrylic acid nanocomposite hydrogel stationary phase (CDs/hydrogel@SiO2) was prepared. CDs act as the macroscopic cross-linking agents to form a cross-linked network with polyacrylic acid chains through physical cross-linking by hydrogen bonding and chemical cross-linking by amidation and esterification reactions, which not only improve the swelling property of the hydrogel but also increase its stability. Additionally, the introduction of CDs with multifunctional groups modulates the hydrophilic-hydrophobic balance of the hydrogel that also imparts good hydrophobicity to the composite hydrogel. Through the study of retention mechanism and influencing factors, it is certificate that the CDs/hydrogel@SiO2 has mixed-mode chromatographic performance. Furthermore, the CDs/hydrogel@SiO2 column shows great potential for the determination of organic contaminants in environmental water samples. SignificanceThis work confirms the potential application of CDs/hydrogel composite for the separation of various samples and provides the possibility of developing CDs based nanocomposite hydrogel in the field of liquid chromatography. Introducing CDs into hydrogel can open up a new way for nanocomposite hydrogels to be used in HPLC, which expands the advance of hydrogel and CDs in separation field.

Porous organic polymers-based fluorescent chemosensors for Fe(III) ions-a functional mimic of siderophores.

Extended organic polymers such as amorphous Covalent Organic Polymers (COPs) and crystalline Covalent Organic Frameworks (COFs) are emerging functional polymeric materials that have recently been shown promises as luminescent materials for chemosensing applications. A wide variety of luminescence COPs and COFs have been synthesized and successfully used as fluorescence-sensing materials for hazardous environmental pollutants and toxic contaminants. This review exemplifies various COPs and COFs-based fluorescence sensors for selective sensing of Fe(III) ions. The fluorescence sensors are sorted according to their structural features and each section provides a detailed discussion on the synthesis and fluorescence sensing ability of different COPs and COFs towards Fe(III) ions. Also, this review highlights the limitations of the existing organic polymer-based chemosensors and future perspectives on translating COPs and COFs-based fluorescence sensors for the practical detection of Fe(III) ions.

Research Advances in Superabsorbent Polymers.

Superabsorbent polymers are new functional polymeric materials that can absorb and retain liquids thousands of times their masses. This paper reviews the synthesis and modification methods of different superabsorbent polymers, summarizes the processing methods for different forms of superabsorbent polymers, and organizes the applications and research progress of superabsorbent polymers in industrial, agricultural, and biomedical industries. Synthetic polymers like polyacrylic acid, polyacrylamide, polyacrylonitrile, and polyvinyl alcohol exhibit superior water absorption properties compared to natural polymers such as cellulose, chitosan, and starch, but they also do not degrade easily. Consequently, it is often necessary to modify synthetic polymers or graft superabsorbent functional groups onto natural polymers, and then crosslink them to balance the properties of material. Compared to the widely used superabsorbent nanoparticles, research on superabsorbent fibers and gels is on the rise, and they are particularly notable in biomedical fields like drug delivery, wound dressing, and tissue engineering.

Recent Developments in Polyurea Research for Enhanced Impact Penetration Resistance and Blast Mitigation.

Polyurea has gained significant attention in recent years as a functional polymer material, specifically regarding blast and impact protection. The molecular structure of polyurea is characterized by the rapid reaction between isocyanate and the terminal amine component, and forms an elastomeric copolymer that enhances substrate protection against blast impact and fragmentation penetration. At the nanoscale, a phase-separated microstructure emerges, with dispersed hard segment microregions within a continuous matrix of soft segments. This unique microstructure contributes to the remarkable mechanical properties of polyurea. To maximize these properties, it is crucial to analyze the molecular structure and explore methods like formulation optimization and the incorporation of reinforcing materials or fibers. Current research efforts in polyurea applications for protective purposes primarily concentrate on construction, infrastructure, military, transportation and industrial products and facilities. Future research directions should encompass deliberate formulation design and modification, systematic exploration of factors influencing protective performance across various applications and the integration of numerical simulations and experiments to reveal the protective mechanisms of polyurea. This paper provides an extensive literature review that specifically examines the utilization of polyurea for blast and impact protection. It encompasses discussions on material optimization, protective mechanisms and its applications in blast and impact protection.

Obtaining micrometric-scale hollow fibers from wastes aged coir by oxidative chloro-sulfonation of lignin: HClO/H2SO4

Coconut fiber is a lignocellulosic material extracted from the coconut mesocarp. Due to its mechanical properties, coconut fiber has been used as reinforcement in composite materials, which contrasts with a relatively small number of studies where coconut fiber is evaluated as a functional polymeric material. In this research, the extraction and transformation of aged coconut biofibers are proposed for their use as substrate/support into making of functional polymers, specifically for slow release of fertilizers. An interesting property of this material is its hollow-type morphology at micrometric scale. Thus, coconut biofibers (BFs) were mechanically extracted and delignified using mixed-oxidizing system constituted by NaClO and H2SO4 at different pH values (2.0 ≤ pH ≤ 12.0). BFs were thermal, spectroscopic and functionally characterized by different techniques, including infrared and ultraviolet-visible spectroscopies, thermogravimetric analysis, scanning electron microscopy, among others. The bleaching of the fibers and the removal of lignin were evidenced by microscopy. The best results of this stage were seen at pH 4.0, 7.0 and 8.0, being possible obtain different materials depending on three acidity regimens (2.0 ≤ pH ≤ 4.0, 4.0 < pH ≤ 8.0 and 8.0 < pH ≤ 12.0). In addition, delignification achieved is function on pH with a value close to 80 % according to the change of surface color intensity. It is concluded that coconut biofibers are natural structure which can be used as support for the making of functional materials.

Engineered Immobilised Organocatalysts for the Synthesis of Chiral Amines

AbstractThe art of tuning functional polymeric materials through the covalent incorporation of organocatalysts lies at the core of creating asymmetric immobilized chiral catalysts that mimic the enzymatic action. Herein, we explore diverse synthetic techniques to immobilize l‐proline‐derived N‐carbonyl amides on functional polymeric matrices, transforming them into chiral Lewis bases for facilitating the asymmetric reduction of ketimines with HSiCl3. A comprehensive examination of the design factors, encompassing linker selection, anions, and polymeric support characteristics, enables precise adjustment of steric and electronic features in these immobilized catalysts. This approach establishes structure‐performance relationships, ultimately enabling the development of an engineered immobilized organocatalytic system that meets the desired criteria for activity, stability, and selectivity.

Molecular dynamics simulation and performance analysis of polyimide/aramid blends.

Polyimide (PI) and aramid, as functional polymer materials, have significant application prospects in special fields such as fire prevention and arc resistance. Blends of materials can not only improve the physical and chemical properties of a single material, but also save costs, so in order to improve the performance of polyimide, it is of great practical importance to study the properties of PI and aramid blends. Molecular dynamics simulation results showed that the two materials are compatible. The solubility parameters of PI tend to stabilize when the polymerization degree exceeded 10; aramid-1313 and aramid-1414 tend to stabilize at polymerization degrees of 10 and 15 or more, respectively. On this basis, the binding energy, diffusion coefficient, and mechanical properties of PI/aramid-1313 and PI/aramid-1414 blends with different mass ratios were analyzed. It was found that with the continuous increase of aramid content, the binding energy of the blends continue to improve, limiting the gas molecules diffusion ability. The mechanical properties of the materials also continue to improve. The simulation results provided in this paper can provide theoretical guidance for experiments on PI blends and shorten the research time and cost. To investigate the properties of PI and aramid blends, the PI/aramid composite system models were constructed using the Amorphous Cell module in Materials Studio software. Subsequently, molecular dynamics simulations of the PI/aramid composite system were performed using the Forcite module, while the interactions between atoms and molecules were described using the COMPASS II force field.

Photo- and halochromism of spiropyran-based main-chain polymers.

Advanced functional polymeric materials based on spiropyrans (SPs) feature multi-stimuli responsive characteristics, such as a change in color with exposure to light (photochromism) or acids (halochromism). The inclusion of stimuli-responsive molecules in general - and SPs in particular - as main-chain repeating units is a scarcely explored macromolecular architecture compared to side chain responsive polymers. Herein, we establish the effects of substitution patterns on SPs within a homopolymer main-chain synthesized via head-to-tail Acyclic Diene METathesis (ADMET) polymerization. We unambiguously demonstrate that varying the location of the ester group (-OCOR) on the chromophore, which is essential to incorporate the SPs in the polymer backbone, determines the photo- and halochromism of the resulting polymers. While one polymer shows effective photochromism and resistance towards acids, the opposite - weak photochromism and effective response to acid - is observed for an isomeric polymer, simply by changing the position of the ester-linker relative to the benzopyran oxygen on the chromene unit. Our strategy represents a simple approach to manipulate the stimuli-response of main-chain SP bearing polymers and highlights the critical importance of isomeric molecular constitution on main-chain stimuli-sensitive polymers as emerging materials.

Functional 3D-Printed Polymeric Materials with Metallic Reinforcement for Use in Cut-Resistant Gloves.

Given the mechanical hazards occurring in the workplace, cut resistance is a particularly important protective parameter. 3D printing is an innovative technology that has recently garnered great interest. It enables the creation of functional polymeric materials with metal reinforcement for use in cut-resistant gloves. The present study characterized and tested 3D-printed polymeric materials intended for such applications. The materials were made from commercially available 3D printing polymer filaments. Metallic reinforcement (stainless steel wire with a diameter of 0.04 mm) was added to the two selected materials (thermoplastic polyurethane and FiberFlex30D). Tests have shown that materials containing metallic reinforcement demonstrate higher mechanical resistance. Cut resistance increased by 70%, and the force needed to tear the sample increased by over 20% compared to the pure polymer. The presence of metallic reinforcement strengthens the structure of the material and changes the cracking mechanism. The tearing occurs in the test area, not in the bell area. These findings demonstrate the feasibility of applying functional 3D-printed polymeric materials with metal reinforcement in cut-resistant gloves.

Preparation and performance of intumescent water-based coatings with both thermal insulation and flame retardant functions

Functional flame retardant polymer materials are of great strategic relevance in reducing energy consumption in the wake of accelerated advances in materials science. In this paper, boehmite sol was employed to modify the surface of hollow glass microspheres (HGMs), self-designed a new type of intumescent flame retardant with melamine polyphosphate and starch (M-S system), which subsequently achieved synergistic flame retardant effects and produced high-performance water-based HGMs@Al2O3/M-S composite coatings that could be successively manufactured. As revealed from findings, HGMs@Al2O3 retained the fundamental structure and characteristics of HGMs and enhanced the interfacial compatibility with the water-based polymer matrix. The thermal conductivity of 0.097 W/(m·K) was achieved at 7 wt% HGMs@Al2O3, which notably strengthened the fire resistance of the coating when compounded with 20 wt% M-S. HGMs@Al2O3 also acted as a catalyst for carbon formation and achieves self-extinguishing off fire when the LOI value reached 36 % and UL94 passed the V-0 test. The maximum pyrolysis temperature of the HGMs@Al2O3/M-S composite coatings was 410.1 °C. The results of conical calorimetry indicate that the HRR were reduced by 76.9 % and the THR by 83.8 %, the superior smoke suppression performance of the material. FPI and FGI were 0.21 m2s/kW and 3.02 kW/m2/s separately, indicating a significant improvement in the fire performance of the material, with high residual carbon strength. When burned, HGMs@Al2O3 migrates to the surface of the material and acts as a flame retardant. It demonstrates that the material is superior to previous resemble products and has tremendous potential for application and further industrialization.

Applications of Supramolecular Polymers Generated from Pillar[n]arene-Based Molecules.

Supramolecular chemistry enables the manipulation of functional components on a molecular scale, facilitating a "bottom-up" approach to govern the sizes and structures of supramolecular materials. Using dynamic non-covalent interactions, supramolecular polymers can create materials with reversible and degradable characteristics and the abilities to self-heal and respond to external stimuli. Pillar[n]arene represents a novel class of macrocyclic hosts, emerging after cyclodextrins, crown ethers, calixarenes, and cucurbiturils. Its significance lies in its distinctive structure, comparing an electron-rich cavity and two finely adjustable rims, which has sparked considerable interest. Furthermore, the straightforward synthesis, uncomplicated functionalization, and remarkable properties of pillar[n]arene based on supramolecular interactions make it an excellent candidate for material construction, particularly in generating interpenetrating supramolecular polymers. Polymers resulting from supramolecular interactions involving pillar[n]arene find potential in various applications, including fluorescence sensors, substance adsorption and separation, catalysis, light-harvesting systems, artificial nanochannels, and drug delivery. In this context, we provide an overview of these recent frontier research fields in the use of pillar[n]arene-based supramolecular polymers, which serves as a source of inspiration for the creation of innovative functional polymer materials derived from pillar[n]arene derivatives.