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High‐performance polymers have proliferated in modern society across a variety of industries because of their low density, good chemical stability, and superior mechanical properties. However, while polymers are widely applied, frequent fire disasters induced by their intrinsic flammability have caused massive impacts on human beings, the economy, and the environment. Supramolecular chemistry has recently been intensively researched to provide fire retardancy for polymers via the physical barrier and char‐catalyzing effects of supramolecular aggregates. In parallel, the noncovalent interactions between supramolecular and polymer chains, such as hydrogen bonding, π–π interactions, metal–ligand coordination, and synergistic interactions, can endow the matrix with enhanced mechanical strength. This makes it possible to integrate physical–chemical properties and noncovalent interactions into one supramolecular aggregate‐based high‐performance polymeric system on demand. However, fulfilling these promises needs more research. Here, we provide an overview of the latest research advances of fire‐retardant and high‐strength polymer materials based on supramolecular structures and interactions of aggregates. This work reviews their conceptual design, characterization, modification principles, performances, applications, and mechanisms. Finally, development challenges and perspectives on future research are also discussed. [ABSTRACT FROM AUTHOR]

High energy and power density alkali‐ion (i.e., Li+, Na+, and K+) batteries (AIBs), especially lithium‐ion batteries (LIBs), are being ubiquitously used for both large‐ and small‐scale energy storage, and powering electric vehicles and electronics. However, the increasing LIB‐triggered fires due to thermal runaways have continued to cause significant injuries and casualties as well as enormous economic losses. For this reason, to date, great efforts have been made to create reliable fire‐safe AIBs through advanced materials design, thermal management, and fire safety characterization. In this review, the recent progress is highlighted in the battery design for better thermal stability and electrochemical performance, and state‐of‐the‐art fire safety evaluation methods. The key challenges are also presented associated with the existing materials design, thermal management, and fire safety evaluation of AIBs. Future research opportunities are also proposed for the creation of next‐generation fire‐safe batteries to ensure their reliability in practical applications. [ABSTRACT FROM AUTHOR]

In this work, the organocatalytic strategy for the ring‐opening copolymerization (ROCOP) of 3,5‐anhydro‐D‐xylose oxetane 1 and various anhydrides has been demonstrated by use of phosphazene base (P1) and triethyl borane (TEB). The ROCOP proceeds efficiently to generate sugar‐derived polyesters with perfectly alternating sequence distribution, controlled molar masses, and moderate dispersity. These polyesters show good thermal stability (Tmax > 320°C) and adjustable glass transition temperatures (Tg 70 ~ 110°C) with the variation of anhydrides. This work provides efficient organocatalyst for the selective copolymerization for biomass‐derived degradable polyesters. [ABSTRACT FROM AUTHOR]

Biodegradable polymeric materials with high strength and outstanding toughness are necessary for real‐world applications in the fields of electronics, electrics, and packaging. Unfortunately, such performance portfolios in polymers remain challenging to achieve due to their different governing mechanisms. Inspired by the hydrogen‐bond (H‐bond) cross‐linking structure of spider silk, herein, strong and tough poly(vinyl alcohol) (PVA) composites with β‐cyclodextrin as a cross‐linker are developed. Benefiting from the H‐bond cross‐linking effect, the addition of 1.0 wt% of β‐cyclodextrin enables PVA to achieve a high tensile strength of 136.5 MPa, and a high elastic modulus of 3.0 GPa, in combination with a good toughness of 82.1 MJ m−3. In addition, the presence of β‐cyclodextrin improves the biodegradability of PVA composite by decreasing its crystalline size. Furthermore, PVA/β‐cyclodextrin composite combined with MXene has great potential as a sensor material for humidity and strain detection. This proof‐of‐concept opens numerous opportunities to create strong, tough, and biodegradable polymers for packing and sensing applications. [ABSTRACT FROM AUTHOR]

Frequent fire disasters have caused massive impacts to the environment, human beings, and the economy. MXene has recently been intensively researched as potential flame retardants to provide passive fire protection for other materials via its physical barrier and catalyzing carbonization effects. In parallel, MXene has also demonstrated a great promise for creating early fire warning sensors, which is an emerging field that has the potential to provide active fire response through its thermoelectric effect. This makes it possible to integrate passive fire retardancy and active fire warning into one MXene‐based fire protection system on demand. However, fulfilling these promises needs more research. Herein, an overview of passive flame‐retardant materials and next‐generation smart fire warning materials/sensors based on MXene and its derivatives is provided. This study reviews their conceptual design, characterization, modification principles, performances, applications, and mechanisms. A discussion of the challenges that need to be solved for their future practical applications and opportunities is also presented. [ABSTRACT FROM AUTHOR]

In this work, we report the synthesis and polymerization performances of terpenoid‐derived camphoric anhydride (CA). Utilizing simple organo‐base tBuP2 as the catalyst, CA can polymerize with various epoxides by efficient and controlled ring‐opening alternating copolymerization (ROAC) to afford perfectly alternating poly(CA‐alt‐epoxide). Kinetic study shows that the polymerization proceeds following zero‐order dependence on the concentration of CA. The self‐switchable terpolymerization from the mixture of CA, propylene oxide (PO) and ε‐caprolactone (CL) is conducted under the catalysis of tBuP2. First, ROAC of CA and PO is carried out exclusively with benzyl alcohol as initiator. Then, block copolymer (BCP) poly(CA‐alt‐PO)‐b‐PCL is obtained via the sequential polymerizations after the complete consumption of CA. The followed ring‐opening polymerization (ROP) of CL is initiated by the terminal hydroxyl of the ROAC‐resulted poly(CA‐alt‐PO) polyester without external stimulus. During the process, the excess PO compound remains intact. The one‐pot synthesis displays distinct living nature and perfect chemoselectivity. The as‐prepared terpenoid‐derived alternating and BCP's exhibit elevated thermal properties. [ABSTRACT FROM AUTHOR]

Diabetic nephropathy (DN) is a fatal complication of diabetes and the main cause of end-stage renal disease. Due to the suboptimal effects of current treatments, there is an urgent need to develop new therapeutic strategies for DN. Trametenolic acid (TA), a lanostane-type tetracyclic triterpenoid, is one of the main active ingredients extracted from the natural product Inonotus obliquus. Our study was aimed at clarifying the potential protective effects of TA on DN and its underlying mechanism. In this research, C57BLKS/db (db/db) mice were used as the spontaneous DN model, and TA (10 mg/kg/d) was intraperitoneally injected for 4 consecutive weeks. Ratio of right kidney weight/body weight was calculated, and the contents of serum creatinine (Scr), blood urea nitrogen (BUN), and urine albumin were detected. The activities of superoxide dismutase (SOD) and catalase (CAT) and the contents of reductive glutathione (GSH) and malondialdehyde (MDA) were measured. The histopathological changes of renal tissues were observed by hematoxylin and eosin (HE), periodic acid-Schiff (PAS), and Masson staining. The protein expressions of nuclear factor erythroid 2-related factor 2 (Nrf2), heme oxygenase-1 (HO-1), NAD(P)H:quinone oxidoreductase-1 (NQO-1), nuclear factor kappa B (NF-κB), proinflammation cytokine tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), interleukin-1β (IL-1β), Nephrin, and Podocin were detected by western blot assay. Immunohistochemistry was utilized to detect expressions of collagen III (COL-III) and fibronectin (FN). Our results showed that TA administration significantly reduced the ratio of right kidney weight/body weight, BUN, Scr, and urine albumin levels and alleviated the histopathological changes of DN mice. Moreover, TA administration remarkably increased GSH content and SOD and CAT activities and decreased MDA content. Western blot assay demonstrated that TA activated Nrf2 signaling and increased the expression of downstream antioxidant enzymes HO-1 and NQO-1. Further studies illustrated that NF-κB signaling was inhibited, and downstream proinflammation cytokine expressions of TNF-α, IL-6, and IL-1β were also downregulated. In addition, we also found that TA administration significantly increased the expression of nephrin and podocin proteins and reduced the protein expression of COL-III and FN. These findings suggested that TA exhibited a renoprotective effect by ameliorating oxidative stress and inflammation via Nrf2/HO-1 and NF-κB signaling pathways. [ABSTRACT FROM AUTHOR]

In this article, a solid-state mechanochemical method based on a pan-mill equipment was used to prepare 60 wt % loading of wood flour (WF) incorporated polypropylene (PP) wood-plastic composite (WPC) with good comprehensive performance. The particle size distribution, crystallization, microstructure, and properties of the prepared WPC were accordingly investigated. The results show that under co-effects of the strong shear force field of pan milling and the compatibilization of PP grafted maleic anhydride (PP-g-MAH), the mixture of PP and WF is effectively pulverized and homogeneously mixed. Meanwhile, the WF particles are adequately activated by exposure of their characteristic functional groups, which is beneficial to the interfacial mechanochemical reaction. PP-g-MAH and PP prove to be in situ grafted onto WF particles surface during pan milling, thus resulting in the substantial enhancement in both the dispersion of the added WF fillers in PP matrix and the interfacial bonding. The mechanochemical effects of pan milling could also remarkably promote the heterogeneous nucleation effect of WF particles on PP crystallization and influence the dynamic mechanical behavior of composite. Compared with the unmilled and uncompatibilized composite, the milled and compatibilized WPC material possesses greatly enhanced mechanical performance and shows good application prospects. [ABSTRACT FROM AUTHOR]

Highlights Polylactide (PLA) biocomposite filaments containing hemp hurd (HH) of variable particle size were evaluated in comparison with injection‐molded counterparts using single/twin screw extrusion in this study. HH particle size (35, 50, and 160 μm) was parametrically investigated for its efficacy within PLA/HH biocomposites and fused filament fabrication (FFF)‐printed parts by assessing its effect on performance through rheological, microstructural, mechanical, and surface finish analyses. In addition, melt flow indexing, rheometry, scanning electron microscopy, mechanical testing, and x‐ray computed tomography were utilized to analyze microstructure, mechanical performance, and surface roughness. With an increase in particle size of the HH, the corresponding biocomposites showed increased flowability, and the injection‐molded specimens showed increased impact strength. The FFF printing of the biocomposite filament presented no challenges, and the mechanical properties of FFF parts enhanced with a particle size smaller than the printed layer thickness. Compared with injection‐molded parts, FFF‐printed samples showed higher impact strength. The FFF‐printed PLA/HH biocomposite samples showed considerable potential over their injection molded alternatives for low‐volume specialized applications. Polylactide (PLA)/hemp hurd (HH) biocomposite filaments with different particle sizes of HH were developed. Melt flow and impact strength increased when HH particle size increased. 3D‐printed part porosity and roughness increased when HH particle size increased. Higher HH particle size enhanced the mechanical performance of 3D‐printed parts. 3D‐printed parts exhibited higher impact strength than injection molded parts [ABSTRACT FROM AUTHOR]