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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2019 · IF 6.361

Highly fluorinated F-APP-TiO2 particle with hierarchical core-shell structure and its application in multifunctional superamphiphobic surface: Mechanical robustness, self-recovery and flame retardancy

Fengyi Wang,Daheng Wang,Zhiguang Guo

Functional superamphiphobic coatings have garnered massive concern due to their promising application in oil transportation and anti-contamination, which call for the requirements of mechanical stability and flame retardancy. Herein, a novel superamphiphobic PVT/F-APP-TiO 2 hybrid coating with excellent mechanical stability and flame retardancy was fabricated using fluorinated PVT polymer adhesive and highly fluorinated ammonium polyphosphate/TiO 2 (F-APP-TiO 2 ) particles with hierarchical core-shell structure. The synthetic mechanism, surface structure, chemical composition of the F-APP-TiO 2 particles were investigated by Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS), respectively. The PVT/F-APP-TiO 2 coatings exhibited excellent superamphiphobicity, anticontamination and self-cleaning property. Good mechanical stability of PVT/F-APP-TiO 2 coatings was verified by mechical damage tests including sand paper abrasion, tape-peeling and water-impacting tests. Further, the PVT/F-APP-TiO 2 coatings showed excellent flame retardancy and self-recovery ability. The PVT/F-APP-TiO 2 coatings with versatile abilities exhibited promising potential to achieve numerous applications in water-oil proof, fireproof and oil transportation materials.

CAS / MDL: 78560-45-9
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RSC Advances · 2014 ·Vol. 4 ·期 63 ·33466-33473 · IF 3.708

The efficient hydroxyalkylation of phenol with formaldehyde to bisphenol F over a thermoregulated phase-separable reaction system containing a water-soluble Brønsted acidic ionic liquid

Qing Wang,Zhi Min Wu,Yongfei Li,Ying Tan,Ning Liu,Yuejin Liu

The efficient hydroxyalkylation of phenol with formaldehyde to bisphenol F over a thermoregulated phase-separable reaction system containing a water-soluble Brønsted acidic ionic liquid was studied. The reaction system containing the water-soluble IL showed thermoregulated biphasic behavior with change of the alkyl chain length of IL, temperature and water amount. Four types of imidazolium-, ammonium-, phosphonium- and pyridinium-based water-soluble ionic liquids with different anions of dihydrogen phosphate [H2PO4]−, acetate [CH3COO]− and hydrogen sulfate [HSO4]− were used as both Brønsted acidic catalysts and thermoregulated solvents. Among them, [C6MIM][HSO4] gave a high yield of 80.5% and a selectivity of 96.9% for bisphenol F, and the optimal reaction conditions were stirring speed 450 rpm, phenol–formaldehyde ratio 6 : 1, IL catalyst molar concentration 12.5%, reaction temperature 90 °C and reaction time 1 h. [C6MIM][HSO4] could be recovered by simple decantation and could retain its original activity even after six recycling-uses [CnMIM][HSO4] with the alkyl chain length n = 6 found to be the most suitable for the synthesis of bisphenol F because of both the formation of a thermoregulated monophasic reaction system at 90 °C to enhance the reaction efficiency and as a thermoregulated phase-transition solvent to facilitate its recovery from the reaction system.

CAS / MDL: 616-47-7
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Journal of Materials Chemistry A · 2024 · IF 10.7

Optimizing thermal and dielectric properties of ethylene-tetrafluoroethylene (ETFE)/h-BN composites via interface engineering: activation of C–F bonds on ETFE for surface grafting

Miao Wang,Yijin He,Xiaoyu Yang,Xuhui Hou,Wenxuan Li,Shaobo Tan,Zhicheng Zhang

With the increasing demand for dielectric materials in high-frequency microwave applications, fluoropolymer-based dielectric materials have been widely utilized due to their excellent dielectric and insulation properties. However, the low thermal conductivity limits their ability to meet the thermal dissipation requirements during high-frequency and high-speed signal transmission. The present study introduces a pioneering interface engineering strategy wherein C–F bonds on the surface of ethylene-tetrafluoroethylene copolymer (ETFE) are photo-catalytically activated, enabling successful grafting of poly(glycidyl methacrylate) (PGMA) chain segments. Subsequently, the resulting graft copolymers are blended with thermally conductive h-BN filler to prepare composite dielectric materials. The results demonstrate that the incorporation of PGMA segments significantly enhances the interfacial compatibility between the ETFE matrix and h-BN filler, resulting in composites with a dense microstructure and outstanding dielectric and thermal properties. At a filler content of 30 vol%, the ETFE-g-PGMA@BN composite achieves an in-plane thermal conductivity of 4.2 W (m K)−1 and a through-plane thermal conductivity of 0.77 W (m K)−1. Moreover, at 1 GHz, the composite exhibits a dielectric constant of 2.2 and a dielectric loss of 0.004. This work presents a novel interface design strategy for surface modification of PTFE-based fluoropolymers, expanding their potential applications in printed circuit boards (PCBs) and providing a new direction for the design of polymer-based dielectric materials.

CAS / MDL: 10043-11-5
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JOURNAL OF FOOD SCIENCE · 2025 ·Vol. 90 ·期 2 ·e17660 · IF 3.4

Analysis of dynamic flavor changes of volatile and non-volatile fractions analysis of black qingke (Hordeum vulgare L. var. nudum Hook. f.) during steaming process

Junyi Wang,Ruifang Wang,Yan Gao,Jing Wang,Lina Qiao,Huijuan Li,Guohua Zhao,Ning Zhang,Hitao Chen,Jie Sun,Shuqi Wang

Qingke ( Hordeum vulgare L. var. nudum Hook. f.) is a cereal of Gramineae, and it is an indispensable food crop for people in the Qinghai—Tibetan Plateau of China. This work focused on the dynamic changes of volatile and non-volatile fractions of qingke (Heilaoya), that is, black qingke, during steaming, and the flavor variations were discussed combined with their correlation. According to the results of sensory analysis, it revealed that the rice and sweet aroma of black qingke increased with the extension of steaming time and reached the maximum at 60 min, whereas the grassy aroma decreased. Besides, a total of 43 aroma fractions were identified by gas chromatography–olfactometry–mass spectrometry, with the largest quantity showing up at 60 min. In addition, the overall flavor of black qingke became more abundant after steaming for 40–60 min. Furthermore, combined with the changes of the non-volatile substances, it was inferred that Maillard and Strecker reactions occurred between reducing sugars and amino acids, and the fractions, such as 2-acetylthiazole, 2-methylpyrazine, 2-pentylfuran, and furfural, were generated. These components mainly presented notes of baked, rice, and grain. In addition, the fatty acids undergo oxidative degradation to generate hexanal and ( E,E )-2,4-decadienal. These results can provide a theoretical basis for the flavor quality control and industrial production of qingke.

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CHEMICAL ENGINEERING SCIENCE · 2025 · IF 4.3

High-performance F, Mn co-doped VO2(B) cathode material in the form of multilayered nanosheets curled rods and its aqueous zinc ion battery applications

Changqing Yuan,Xiaorong Meng,Han Shen,HaoHao Wei

To address the shortcomings of VO 2 (B) when utilized as cathode materials for aqueous zinc ion batteries (AZIB), this study prepared a fluorine and manganese co-doped VO 2 (B) with a nanorod-like structure, formed from convoluted multilayered nanosheets, was synthesized via a solvothermal method. It was established that F and Mn doping effectively broadens the lattice structure and tunneling space of VO 2 (B) and induces lattice distortion of VO 2 (B) through the high electronegativity of F element, leading to the ductile growth of FMVO into a nanorod-like structure made of multilayered ultrathin nanosheets curled. The increased tunneling space and active sites of FMVO, compared to pure VO 2 (B), significantly enhanced the de-embedding rate of Zn 2+ and reduced diffusion resistance. The specific capacity of F 0.06 M 0.02 VO is 523.92 mAh/g (0.2 A/g) with 88.64 % capacity retention after 2,000 cycles (5 A/g). This research provides a novel approach to the development of cathode materials for AZIB.

CAS / MDL: 1314-62-1 54010-75-2
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LWT-FOOD SCIENCE AND TECHNOLOGY · 2026 · IF 7.1

Unveiling green-to-reddish-brown color transition mechanisms of star anise (Illicium verum Hook. f.) during drying: From oxidative polymerization of catechin to intelligent quality monitoring

Silei Zhang,Qingbo Huang,Xiangmin Kuang,Chaofan Guo,Yongli Jiang,Fujie Zhang,Sakamon Devahastin,Junjie Yi

Oxidative polymerization of catechins drove the green-to-brown color transition. • Electrolyzed water with ultrasound improved drying efficiency and flavor retention. • More extensive cellular disruption contributed to accelerated moisture migration. • Color, aroma, and moisture changes closely reflected quality changes during drying. • Artificial neural network most accurately predicted moisture and catechin contents. Color is critical determinant of market grade and commercial value of star anise ( Illicium verum Hook. f.). However, mechanisms underlying its characteristic green-to-reddish-brown transformation during processing remain insufficiently understood. The present study investigated color evolution of star anise by comparing ultrasound-assisted electrolyzed water treatment (UEWT) with conventional hot-water blanching (HWB) using framework combining drying kinetics, E-nose, LF-NMR, untargeted LC-MS data as well as machine learning modeling. UEWT significantly enhanced drying efficiency, shortening drying time to 8 h compared to 13 h in case of HWB. LF-NMR spectra revealed that UEWT maintained distinct water mobility profiles, effectively reducing internal mass transfer resistance. UEWT also intensified the chromatic transition, as evidenced by a decline in L* , rapid increases in a* and BI, a greater Δ E , an overall decrease in H , and higher late-stage C* values than those observed under HWB. Catechin depletion, accompanied by formation of oligomeric oxidation products, represents key transformation pathway associated with color development. Among the evaluated machine learning models, ANN-based model exhibited superior performance, achieving high prediction accuracy for both moisture content ( R 2  > 0.98) and catechin content ( R 2  > 0.92). These findings provide new insights into physicochemical basis of color formation and offer practical strategy for real-time quality control during industrial drying of aromatic crops. Download: Download high-res image (294KB) Download: Download full-size image

CAS / MDL: 7647-14-5
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DIAMOND AND RELATED MATERIALS · 2025 · IF 5.1

Construction of a novel point-layer structure BNNSs/GQDs composites and research on the regulation of its microwave absorption performance by N and F-doped GQDs

Qi Hu,Chenhao Xu,Yulong Hua,Cunkang Qi,Jing Zhang,Yuemin Wang,Chengchun Tang

To explore the improvement of microwave absorption performance of boron nitride nanosheets (BNNSs) after doping with graphene quantum dots (GQDs). Herein, a series of point-layer structure BNNSs supported by GQDs composite absorbing materials were designed and prepared. The influence of the substrate on the wave absorption intensity was investigated by loading the same GQDs with BNNSs of different scales. Among them, the BG-1400 with BNNSs-1400 as the substrate and GQDs as the load has the best microwave absorption performance. Its minimum reflection loss ( RL min ) reaches −60.3 dB and the effective absorption frequency band is 8.5 GHz. In order to further analyze the factors influencing the effective absorption frequency bands of BNNSs/GQDs composites, BNG-1400 and BFG-1400 were prepared by loading N-GQDs and F-GQDs respectively on the BNNSs-1400 substrate, and their RL min and effective absorption frequency bands were -57.3 dB, −57.7 dB and 11.3 GHz, 13.4 GHz, respectively. The effective absorption frequency bands of BNG-1400 and BFG-1400 have been significantly improved compared with BG-1400.This indicates that the substrate size of the BNNSs/GQDs composite material can control its absorption intensity, while different doped elements in GQDs can adjust its effective absorption frequency band. This discovery lays the foundation for the research on the controllable adjustment of the wave absorption performance of BNNSs/GQDs composite absorbing materials.

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JOURNAL OF ALLOYS AND COMPOUNDS · 2025 · IF 6.3

Oxygen loss mitigation and structural stability via synergistic Zr/F dual-doping in O3 type Ni/Mn based layered oxide for sustainable sodium-ion batteries cathodes

Xinwei Xie,Yaoliang Huang,Li Xu,Guangyu Luo,Haifeng Liu,Xinlong Zhang,Jinyue Yang,Junze Lei,Xiaoyuan Yu

O3-type Ni/Mn-based transition metal oxides have garnered significant interest as cathode materials for sodium-ion batteries (SIBs) due to their high specific capacity and abundant resources. However, their commercialization application has been impeded by rapid capacity fading owing to structural degradation, gas evolution, irreversible phase transitions during charge/discharge cycling. Herein, The Zr 4 + /F - dual-doped strategy is developed to boost the Na-storage performance of Ni/Mn-based O3-NaNi 0.3 Fe 0.1 Mn 0.47 Cu 0.1 Zr 0.03 O 2-x F x (NFMCZF-x) layered oxide cathode material prepared by high temperature calcination method. Structural and electrochemical analyses reveal that Zr⁴⁺ doping expands Na⁺-layer spacing and F⁻ doping strengthens transition metal-oxygen bonds. These synergistic effects of Zr 4+ /F - dual-doping is benefit to suppressing O3↔P3 phase transitions, Jahn-Teller distortion and irreversible oxygen redox. Thus, the optimized NFMCZF-0.03 cathode delivers high specific capacity (178 mAh g −1 at 0.1 C) and excellent cycling stability (72 % capacity retention after 100 cycles at 1.0 C). This study establishes dual doping as an effective strategy for developing Ni/Mn-based layered oxide as high-performance cathodes for SIBs.

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Food and Bioprocess Technology · 2015 ·Vol. 8 ·期 5 ·1011-1019 · IF 2.691

Effects of Combined Aqueous Chlorine Dioxide and Chitosan Coatings on Microbial Growth and Quality Maintenance of Fresh-Cut Bamboo Shoots (Phyllostachys praecox f. prevernalis.) During Storage

Yang Huqing,Zheng Jianying,Huang Chengqian,Zhao Xiaofei,Chen Huiyun,Sun Zhidong

This study was conducted to investigate the effects of aqueous chlorine dioxide (ClO 2 ) combined with chitosan coating on microbial growth and quality maintenance of fresh-cut bamboo shoots during cold storage. Fresh-cut shoots respiration rate, weight loss, firmness, lignin, colour, microbial and activities of phenylalanine ammonia lyase (PAL), cinnamyl alcohol dehydrogenase (CAD), peroxidase (POD) and polyphenol oxidase (PPO) were measured. The results indicated that treatment with 28 mg L −1 ClO 2 plus chitosan coating inhibited increase in respiration rate and firmness, delayed browning and lignification and reduced microorganism counts of total aerobic bacteria and yeasts and moulds compared to control treatment. The efficiency was better than that of ClO 2 or chitosan treatment alone. Furthermore, combination of ClO 2 and chitosan inhibited the activities of PAL, CAD, POD and PPO throughout the storage period. Our study suggests that ClO 2 plus chitosan coating treatment may be a promising method of maintaining fresh-cut bamboo shoot quality and extending their postharvest life.

研究领域: 采后生理学 · 食品科学 · 园艺科学 · 食品保鲜
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ACS Applied Polymer Materials · 2025 · IF 4.7

Improving the Performance of 2,9-Didecyldinaphtho[2,3-b:2′,3′-f]thieno[3,2-b]thiophene Organic Thin-Film-Transistors Using Cyclothiocarbonate- and Decyloxytriphenyl-Modified Polymethacrylate Insulators

Bowen Zhang,Yiqi Zhang,Zhanchen Cui,Wei Wang,Zuosen Shi

The threshold voltage and mobility of organic thin-film transistors (OTFTs) are influenced not only by the dielectric constant of the insulating layer but also by the crystallinity at the interface between the semiconductor and the insulating layer. The crystallization of 2,9-didecyldinaphtho[2,3-b:2′,3′-f]thieno[3,2-b]thiophene (C10-DNTT) is driven by molecular fastening effects from its long alkyl chains and π–π* stacking interactions. This work proposes a method utilizing the interaction of interfacial functional groups to create nucleation centers for C10-DNTT, thus reducing grain boundaries. We synthesized the homopolymer poly(4-(1,3-dithia-2thioxocyclopentyl) methacrylate) (P(TCMA)), which possesses side chains with high dipole moment thiocarbonate groups, and the copolymer poly(4-(1,3-dithia-2thioxocyclopentyl) methacrylate-co-10-([1,1’:4′,1″-terphenyl]-3-yloxy) decyl methacrylate) (P(TCMA-co-10TPOMA)), which contains decyloxytriphenyl groups in its side chains. The mobility of OTFT devices increased from 0.84 cm2 V–1 s–1 with cured P(TCMA) as the insulating layer to 2.97 cm2 V–1 s–1 with cured P(TCMA-co-10TPOMA)-5, reaching a maximum of 3.40 cm2 V–1 s–1 when P(TCMA-co-10TPOMA)-15 was used as the insulating layer, making it a promising candidate for direct application in drive units.

CAS / MDL: 106-91-2 62-56-6
研究领域: 材料科学 · 有机电子学 · 聚合物化学 · 薄膜晶体管 · 半导体器件
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JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A · 2023 · IF 4.9

The dependences of mesenchymal stem cells commitments on the size, concentration, internalization and exposure time of Iron Oxide Nanoparticles through F-actin, Lamin A and ROS

Yuying Bai,Dawei Tian,Zhengxin Ren,Dangyang Yue,Qian Ren,Li Pei,Jun Pan

Though magnetic iron oxide nanoparticles (IONPs) are approved for clinical use as contrast agents for MR imaging in United States and Europe, and are widely used to label cells in research, the relationship between IONPs and mesenchymal stem cells (MSCs) is not fully addressed. Here the effects of consistently appeared γ-Fe 2 O 3 on the lineage commitment of MSCs were studied to optimize applications of IONPs in MSCs upon verification of viability. 30 nm 10 μg/mL induced highest promotions on osteogenesis, while 30 and 50 nm of 100 μg/mL elicited most chondrogensis in 14 days, where the effects on ALP, GAG and SOX9 appeared after 7 days, while on RUNX2 came out after 10 days. γ-Fe 2 O 3 enhanced intracellular and extracellular Fe 3+ and ROS, modulated F-actin and decreased Lamin A of MSCs at different time scale. The disturbances of F-actin, Lamin A or ROS altered the effects of γ-Fe 2 O 3 on MSC differentiation. Our results demonstrate that different size, concentration and modulation of γ-Fe 2 O 3 are needed in its MSC applications for bone and cartilage tissues. Furthermore, an undocumented phenomenon that the modulation of F-actin affected the Lamin A expression in MSCs was observed.

CAS / MDL: 14930-96-2 540-72-7
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MOLECULES · 2023 ·Vol. 28 ·期 14 ·5304 · IF 4.6

Fabrication of Composite Gel Electrolyte and F-Doping Carbon/Silica Anode from Electro-Spun P(VDF-HFP)/Silica Composite Nanofiber Film for Advanced Lithium-Ion Batteries

Caiyuan Liu,Xin Fang,Hui Peng,Yi Li,Yonggang Yang

The aim of this work is to effectively combine the advantages of polymer and ceramic nanoparticles and improve the comprehensive performance of lithium-ion batteries (LIBs) diaphragm. A flexible film composed of electro-spun P(VDF-HFP) nanofibers covered by a layer of mesoporous silica (P(VDF-HFP)@SiO2) was synthesized via a sol–gel transcription method, then used as a scaffold to absorb organic electrolyte to make gel a electrolyte membrane (P(VDF-HFP)@SiO2-GE) for LIBs. The P(VDF-HFP)@SiO2-GE presents high electrolyte uptake (~1000 wt%), thermal stability (up to ~350 °C), ionic conductivity (~2.6 mS cm−1at room temperature), and excellent compatibility with an active Li metal anode. Meanwhile, F-doping carbon/silica composite nanofibers (F-C@SiO2) were also produced by carbonizing the P(VDF-HFP)@SiO2film under Ar and used to make an electrode. The assembled F-C@SiO2|P(VDF-HFP)@SiO2-GE|Li half-cell showed long-cycle stability and a higher discharge specific capacity (340 mAh g−1) than F-C@SiO2|Celgard 2325|Li half-cell (175 mAh g−1) at a current density of 0.2 A g−1after 300 cycles, indicating a new way for designing and fabricating safer high-performance LIBs.Keywords:composite materials;electro-spun nanofiber;gel electrolyte;carbonaceous anode;lithium-ion batteries

CAS / MDL: 68-12-2
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