High-Performance Reversible Furan-Maleimide Resins Based on Furfuryl Glycidyl Ether and Bismaleimides.

Two reversible furan-maleimide resins, in which there are rigid -Ph-CH2-Ph- structures and flexible -(CH2)6- structures in bismaleimides, were synthesized from furfuryl glycidyl ethers (FGE), 4,4'-diaminodiphenyl ether (ODA), N,N'-4,4'-diphenylmethane-bismaleimide (DBMI), and N,N'-hexamethylene-bismaleimide (HBMI). The structures of the resins were confirmed using Fourier transform infrared analysis, and the thermoreversibility was evidenced using differential scanning calorimetry (DSC) analysis, as well as the sol-gel transformation process. Mechanical properties and recyclability of the resins were preliminarily evaluated using the flexural test. The results show the Diels-Alder (DA) reaction occurs at about 90 °C and the reversible DA reaction occurs at 130-140 °C for the furan-maleimide resin. Thermally reversible furan-maleimide resins have high mechanical properties. The flexural strength of cured FGE-ODA-HBMI resin arrives at 141 MPa. The resins have a repair efficiency of over 75%. After being hot-pressed three times, two resins display flexural strength higher than 80 MPa.

Role of carbon quantum dots on Nickel titanate to promote water oxidation reaction under visible light illumination.

Water oxidation reaction (WOR) is the heart for overall water splitting owing to its sluggish kinetics. Herein, carbon quantum dots (CQDs) are studied as co-catalyst to promote WOR by loading them on NiTiO3 (NTO) photocatalyst. The performance can be obtained in a fold of 7 compared with pristine NTO in power-based photocatalytic system, and strong stability has received with preserving the output for at least 10 h. The CQDs have also demonstrated to load on NTO based photoanode for WOR, and a 6 times increasement has realized. In-situ characterizations have acquired to study the roles of CQDs for WOR and found that CQDs can facilitate the chemical adsorption of water molecules, and meanwhile promote the formation of hydroxyl radical as transition states of WOR. This demonstration presents a clue to understand the role of carbon in photocatalytic system to promote WOR and encourage its uses for advanced photoredox catalytic reactions.

Long-term scalogram integrated with an iterative data augmentation scheme for acoustic scene classification.

In acoustic scene classification (ASC), acoustic features play a crucial role in the extraction of scene information, which can be stored over different time scales. Moreover, the limited size of the dataset may lead to a biased model with a poor performance for recordings from unseen cities and confusing scene classes. This paper proposes a long-term wavelet feature that captures discriminative long-term scene information. The extracted scalogram requires a lower storage capacity and can be classified faster and more accurately compared with classic Mel filter bank coefficients (FBank). Furthermore, a data augmentation scheme is adopted to improve the generalization of the ASC systems, which extends the database iteratively with auxiliary classifier generative adversarial neural networks (ACGANs) and a deep learning-based sample filter. Experiments were conducted on datasets from the Detection and Classification of Acoustic Scenes and Events (DCASE) challenges. The DCASE17 and DCASE19 datasets marked a performance boost of the proposed techniques compared with the FBank classifier. Moreover, the ACGAN-based data augmentation scheme achieved an absolute accuracy improvement of 6.10% on recordings from unseen cities, far exceeding classic augmentation methods.

High-Safety and Long-Life Silicon-Based Lithium-Ion Batteries via a Multifunctional Binder.

Lithium-ion batteries with high energy density and good safety are in urgent demand nowadays. Silicon has the advantages of high theoretical capacity, low cost, and vast reserves. It is regarded as an ideal anode material for high-energy lithium-ion batteries. Unfortunately, its huge volume change during cycling results in unstable cycle behavior and limits its application. To develop a robust electrode by employing effective binders is still a big challenge. Furthermore, both conventional binders and organic liquid electrolytes bring serious safety risks due to their flammability. Herein, a flame-retardant binder is designed and prepared by cross-linking polyacrylic acid (PAA) with a flame-retardant epoxy resin (FREP) containing phosphorus and nitrogen elements. Compared with PAA, it has better wettability to liquid electrolytes. Moreover, the three-dimensional PAA-FREP polymer binder not only provides sufficient mechanical strength to buffer the volume change of Si powders but also enhances the interfacial adhesion between the active film and Cu current collector via epoxy groups. Most importantly, the FREP component in the binder leads to admirable flame retardance. In these ways, the multifunctional binder exhibits excellent mechanical, electrochemical, and safety performances.

Supramolecular medical antibacterial tissue adhesive prepared based on natural small molecules.

In the field of biomedicine, tissue bio-adhesives require the use of polymer materials with integrated functions to meet changing practical applications. However, the currently available tissue glues cannot balance mechanical properties and biocompatibility. Inspired by the conversion of lipoic acid from small molecular biological sources into high-performance supramolecular polymeric materials, thioctic acid (TA) was modified and polyethylene glycol diacrylate (PEGDA) was introduced. Successfully constructed a dry gel with antibacterial effect and promote infection for wound regeneration. The prepared modified lipoic acid is mixed with PEGDA, melted under mild heating and self-assembled, and then directly extruded on both sides of the wound. It quickly cures at 37 °C and firmly adheres to both sides of the wound. The material exhibits good processability and rapid self-healing ability due to the cross-linked structure of the internal disulfide bonds and thioether bonds. In addition, the characteristics of TA make the prepared xerogels have good tissue adhesion and good antibacterial properties. This work proposes an innovative material with mechanical strength and biocompatible tissue glue, which provides broad prospects for application in wound treatment.

Refining androstenedione and bisnorcholenaldehyde from mother liquor of phytosterol fermentation using macroporous resin column chromatography followed by crystallization.

Androstenedione is an androgen and intermediate in the biosynthesis of most adrenocortical, anabolic, sex and synthetic steroids, such as canrenone, eplerenone, norethindrone and spironolactone. Bisnorcholenaldehyde is an important intermediate in the synthesis of progesterone. This study established an androstenedione and bisnorcholenaldehyde separation method that used a macroporous adsorption resin and an ethanol-water mixture as eluent. The adsorption properties of 12 non-polar or weakly polar macroporous adsorption resins were compared, and three resins exhibited a high adsorption capacity and high desorption rate for both androstenedione and bisnorcholenaldehyde. The three resins were then compared using column chromatography, and one resin was selected and parameters (flow rate, resin size, ethanol concentration and volume) of chromatography were optimized to obtain high purity and recovery. Chromatography eluate was concentrated, dissolved in suitable solvent and crystallized at an optimal temperature to obtain a high purity of both androstenedione and bisnorcholenaldehyde from the same starting material. The levels of androstenedione and bisnorcholenaldehyde in the raw material were 39.78% and 19.15%, respectively. After preparative separation and enrichment by resin column chromatography and crystallization, the purity of androstenedione and bisnorcholenaldehyde was 94.3% and 98.6%, respectively, with their recovery yields of 66.8% and 57.9%, respectively. In addition, the resin maintained over 90% separation efficiency for 5 cycles of adsorption. These results indicated that the combination of macroporous resin chromatography followed by crystallization provide a simple, effective, environmentally friendly and low-cost method for the simultaneous purification of androstenedione and bisnorcholenaldehyde.

[Optimization of preparation of poly ( glycidyl methacrylate-divinylbenzene) monolithic column with orthogonal experiments for separation of small molecules].

A monolithic column of macro porous poly (glycidyl methacrylate-divinylbenzene) (poly(GMA-DVB)) has been prepared by free radical polymerization within the confines of a chromatographic stainless steel tube (50 mm x 4.6 mm). For the best separation and low back pressure, orthogonal experiments were carried out with V (cyclohexanol): V (dodecanol), V (GMA): V (DVB) and BPO dosage as the three main factors. The characteristic feature of the column, including specific surface area, pore volume as well as pore diameter distribution, was studied by scanning electron microscopy (SEM), mercury intrusion porosimetry analysis and BET analysis. The obtained optimum preparation conditions were that the volume ratio of GMA, DVB, cyclohexanol and dodecanol was 0.825: 0.825: 1.32: 2.03 and the BPO dosage was 0.7% (mass percentage), then it was heated at 70 degrees C for 24 h. Using this monolithic column, benzene and ethylbenzene and a drug of oxiracetam can be well separated on a high performance liquid chromatographic (HPLC) system equipped with a ultraviolet (UV) detector at 254 nm. A solution of acetonitrile-water (50 : 50, v/v) for the separation of benzene and ethylbenzene, and acetonitrile-water (80 : 20, v/v) for the separation of oxiracetam were used as mobile phases at a flow rate of 1 mL/min. The theoretical plate number was 37 000 plates/m and the resolution of peak width at half height (R1/2) was 7.14. The separation time was less than 10 min. The monolithic column prepared by this method is reproducible and has high column efficiency. It is an economical method to prepare monolithic column, which can be applied to separate small molecules.

Optimization of Serratia marcescens lipase production for enantioselective hydrolysis of 3-phenylglycidic acid ester.

Lipase production and cell growth of Serratia marcescens ECU1010 were optimized in shake flasks, with lipase production being enhanced 9.5-fold (4,780 U/l) compared with the initial activity (500 U/l). Optimal carbon and nitrogen sources were Tween-80 and peptone, and the optimal ratio of Tween-80 to peptone was 1:3. The optimized cultivation conditions were 25 degrees C and pH 6.5. Lipase activity, particularly specific activity, could be improved by decreasing the cultivation temperature from 35 to 25 degrees C. Enzyme stability was significantly improved by simple immobilization with synthetic adsorption resin no. 8244. After five reaction cycles, enzyme activity decreased only very slightly, while enantioselectivity of the preparation remained constant, and the ees (enantiomeric excess of the remaining substrate) achieved in all cases was higher than 97%. The resin-8244-lipase preparation can be used for efficient enantioselective hydrolysis of trans-3-(4'-methoxyphenyl)glycidic acid methyl ester [(+/-)-MPGM], a key intermediate in the synthesis of Diltiazem.