Novel aerogels based on supramolecular G-quadruplex assembly with intrinsic flame retardancy and thermal insulation.

The construction of supramolecular aerogels still faces great challenges. Herein, we present a novel bio-based supramolecular aerogel derived from G-Quadruplex self-assembly of guanosine (G), boric acid (B) and sodium alginate (SA) and the obtained GBS aerogels exhibit superior flame-retardant and thermal insulating properties. The entire process involves environmentally friendly aqueous solvents and freeze-drying. Benefiting from the supramolecular self-assembly and interpenetrating dual network structures, GBS aerogels exhibit unique structures and sufficient self-supporting capabilities. The resulting GBS aerogels exhibit overall low densities (36.5-52.4 mg/cm3), and high porosities (>95 %). Moreover, GBS aerogels also illustrate excellent flame retardant and thermal insulating properties. With an oxygen index of 47.0-51.1 %, it can easily achieve a V-0 rating and low heat, smoke release during combustion. This work demonstrates the preparation of intrinsic flame-retardant aerogels derived from supramolecular self-assembly and dual cross-linking strategies, and is expected to provide an idea for the realization and application of novel supramolecular aerogel materials.

A graphene@Cu-MOF hybrid synthesized by mechanical ball milling method and its flame retardancy and smoke suppression effect on EP.

The traditional method of preparing graphene will cause serious environmental pollution, and the combustion of polymer materials will seriously harm people's health. In this paper, a Cu-MOF-coated graphene composite flame retardant (G@Cu-MOF) rich in flame retardant elements such as B and N was synthesized through green mechanical ball milling method. Flame retardants reduce the threat to the environment and people's lives and property. After adding 6 wt% G@Cu-MOF, the peak heat release rate, total heat release rate, CO production and CO2 production of epoxy resin (EP) composite samples decreased by 55, 14, 59, and 55%, respectively. This type of Cu-MOF releases incombustible gases such as boron trifluoride (BF3) and ammonia (NH3) during combustion, diluting the concentration of combustible gases and producing copper borate in the condensed phase. Cu2+ is reduced to Cu, and boron compounds are converted into boron oxides. The thermal conductivity of graphene can reduce the temperature of the matrix, and has good flame retardancy. It synergistically acts with Cu-MOF to promote the formation of high-quality residual char, and can significantly inhibit the heat and smoke release of EP. It plays a role in flame retardancy and protecting the substrate from fire. This study provides a new approach for preparing graphene hybrid flame retardants through mechanical ball milling, in order to improve the flame retardancy of EP and suppress the release of smoke and toxic gases.

Abating ammonia emission from poultry manure by Pt/TiO2 modified corn straw.

Poultry manure is a significant source of ammonia (NH3) emissions, which not only poses detrimental impacts on human well-being and the ecological system, but also leads to economic losses in the agricultural industry. Herein, we modified corn straw (CS) with 1 wt% Pt/TiO2 catalysts using a low-temperature partial-oxidation technology to mitigate NH3 emissions from poultry manure. It was found that Pt/TiO2 can enable exothermic processes to occur at lower temperatures by reducing the activation energy. Under optimal modification conditions of 220 °C, the NH3 uptakes of modified CS samples were markedly greater compared to those of the original CS. Addition of 20-50% modified CS to poultry manure resulted in significant reductions of 54.1-98.6% in NH3 emissions compared to the control. Mechanistic studies indicate that NH3 adsorption on the modified CS is mainly driven by the presence of acidic and alkaline functional groups, while surface area and pore structure have a negligible effect. XPS combined with NH3-TPD reveals that the formation of amide and amine bonds contributes to the excellent stability of adsorbed NH3. H2-TPR, O2-TPD, and d-band theory suggest that strong metal-support interactions between Pt and TiO2 could be particularly crucial in catalyzing CS modification. This study proposes an environmentally sustainable and economically viable solution for abating NH3 emissions from poultry manure, thereby addressing crucial environmental and economic concerns in the agricultural sector.

Catalytic modification of corn straw facilitates the remediation of Cd contaminated water and soil.

Turning postharvest residue into high-value-added products is crucial for agricultural waste management and environmental remediation. In this proof-of-concept study, nanosized Pt/TiO2 was used as a model catalyst to modify corn straw (CS) materials through a simple low-temperature oxidation process. This method was demonstrated to be self-sustainable, waste-free, and with high yields. At an optimal temperature of 220 °C, O2 treatment with 1 wt% Pt/TiO2 greatly changed ultra-micropore and mesopore structures, dissolved organic carbon, aromatic contents and surface oxygen (O)-containing functional groups in CS products. This treatment resulted in an approximately 5-fold increase of cadmium (Cd) adsorption from aqueous solution and immobilization rate of 43.1% at 7d for bioavailable Cd in soil. Spectroscopic and linear regression analysis demonstrated that both acidic and basic functional groups in CS contributed to Cd adsorption, suggesting chemical adsorption. According to the d-band theory, the unexpected role of catalysts in CS modification could be associated with dissociative adsorption of molecular O2 on the Pt surface. These results provide insights for the development of economic and sustainable technologies to reutilize agricultural waste biomass for water and soil remediation.

Highly Tough, Stretchable, and Recyclable Ionogels with Crosslink-Enhanced Emission Characteristics for Anti-Counterfeiting and Motion Detection.

Traditional luminescent ionogels often suffer from poor mechanical properties and a lack of recyclability and regeneration, which limits their further application and sustainable development. Herein, a luminescent ionogel with strong mechanical properties and good recyclability has been designed and fabricated by introducing dynamic coordination bonds via in situ one-step crosslinking of acrylic acid in ionic liquid of 1-ethyl-3-methylimidazolium diethylphosphate by zinc dimethacrylate. Due to the special crosslinking of dynamic coordination bonds along with the hydrogen bond interaction, the as-prepared ionogel displays excellent stretchability and toughness, good self-adhesiveness, fast self-healability, and recyclability. Interestingly, the obtained ionogels exhibit tunable photoluminescence caused by the crosslink-enhanced emission (CEE) effect from the coordination bonds. Importantly, ionogels can be applied in information storage, information encryption, anti-counterfeiting due to their simple and in situ preparation method, and their special fluorescence performances. Moreover, an ionogel-based wearable sensor has rapid response time and a high gauge factor of 3.22 within a wide strain range from 1 to 700%, which can monitor various human movements accurately from subtle to large-scale motions. This paper offers a promising way to fabricate sustainable functional ionic liquid-based composites with CEE characteristics via an in situ one-step polymerization method.

Scrophulariae Radix-Atractylodes sinensis pair and metformin inhibit inflammation by modulating gut microbiota of high-fat diet/streptozotocin-induced diabetes in rats.

Introduction: Type 2 mellitus (T2DM), a chronic metabolic disorder, causes severe impairment of patients' quality of life and has attracted global attention. Many studies have suggested the importance of the gut microbiota in the occurrence of T2DM. The Scrophulariae Radix and Atractylodes sinensis (XC) pair, recommended in traditional Chinese medicine (TCM), have been used for treating diabetes for many years. However, research on the role of the XC pair in modulating gut microbial communities is lacking, but it is important to elucidate the underlying mechanism. Methods: In this study, we detected bacterial communities by high-throughput 16S rRNA gene sequencing. Results: The results showed that XC + MET reduced postprandial hyperglycemia and inflammatory response in diabetic rats more effectively than metformin (MET) alone. The XC + MET treatment reshaped the intestinal microbial composition of diabetic rats. XC can help MET regulate carbohydrate, amino acid, and lipid metabolism, particularly the insulin signaling pathway. Discussion: This research would help elucidate potential mechanisms and the treatment methods.

Identifying adsorption sites for Cd(II) and organic dyes on modified straw materials.

Turning agricultural waste into effective remediation materials is a highly promising approach for reducing in-field crop burning and promoting affordable wastewater treatment. This comparative study aims to identify active adsorption sites for methylene blue (MB), crystal violet (CV), and cadmium (Cd) as model pollutants on wheat straw materials modified by a thermal partial-oxidation process. The optimal modification temperature was found to be 160-180 °C for MB and CV adsorption, which is much lower than that of Cd(II) at 220-240 °C. A strong linear correlation exits between total surface group concentrations and Cd(II) uptake, indicating that both acidic and basic functional groups are favourable adsorption sites of Cd(II). By contrast, basic groups generated at higher modification temperatures might have adverse effects on MB and CV adsorption. These results provided mechanistic insights and predictive approach into reuse of agricultural waste for environmental remediation.

Synthesis of a novel phosphazene-based flame retardant with active amine groups and its application in reducing the fire hazard of Epoxy Resin.

A novel compound containing active amine groups of polyphosphazene (PBFA) was successfully synthesized and applied as a reactive flame-retardant additive in epoxy (EP) resin. It was synthesized from N-aminoethylpiperazine and hexachlorocyclotriphosphazene using a simple method, and its structure was well-characterized. The results indicated that introducing PBFA into EP composites significantly improves the resistance to fire and suppresses smoke generation. An EP composite with 9.0 wt% PBFA can pass the vertical burning tests V-0 rating, the peak heat release rate and total heat release of the sample decreased by 46.7% and 29.3%, respectively. Moreover, it decreased the total smoke release by 48.0%. Thermogravimetric analysis showed that the presence of PBFA can accelerate EP decomposition at comparatively low temperatures and lead to the formation of a stable char layer, which protects the matrix from fire, therefore improving the amount of char residue at 800 °C. The degree of small molecule degradation characterized by gas chromatograph/mass spectrometer, which was lower than that of pure EP, demonstrating that PBFA reduces the risk of fire. The glass transition temperature of EP composites increased with the amount of PBFA increasing owing to the presence of active amine groups. Notably, its mechanical properties were not degraded.