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Food Bioscience · 2020 · IF 3.067

Lipase-mediated production of 1-oleoyl-2-palmitoyl-3-linoleoylglycerol by a two-step method

Liang Gao,Xinyi Cheng,Xuwei Yu,Xiaosan Wang,Qingzhe Jin,Xingguo Wang

1-Oleoyl-2-palmitoyl-3-linoleoylglycerol (OPL) is a critical structured lipid in human milk fat and it plays an important role in infants' health. The development of an efficient method for such compound preparation is necessary. In this study, one- and two-step methods for OPL production by enzymatic acidolysis of fractionated palm stearin with mixed acids were compared in solvent-free and solvent systems. The results demonstrated that in the solvent system, the OPL contents by the one- and two-step methods were 45.8% and 56.7%, respectively. In the solvent-free system, the one- and two-step methods resulted in the formation of 43.7% and 54.8% OPL, respectively. Subsequently, acidolysis conditions of the two-step method were optimized. Under the optimum conditions, the content of OPL was 57.7%, and 83.2% of palmitic acid was at the sn-2 position . The prepared OPL has potential to be applied in infant formulas.

✓ 已验证 DOI 高影响因子
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CHEMISTRY & BIODIVERSITY · 2022 ·Vol. 19 ·期 6 ·e202200286 · IF 2.745

Longibrachiamide A, a 20-Residue Peptaibol Isolated from Trichoderma longibrachiatum Rifai DMG-3-1-1

Shu-Hua Zhang,Xian-Lin Yue,Xue Zhao,Jing Tang,Yu Yang,Rui Xu,Hao Ma,Shuai-Ming Zhu,Fu-Yao Luo,Qin Zhang,Guo-Gang Zhang,Chang-Wei Li

Longibrachiamide A ( 1 ), a new 20-residue peptaibol, along with three known ones ( 2 – 4 ), were isolated from the fungus Trichoderma longibrachiatum Rifai DMG-3-1-1, isolated from a mushroom Clitocybe nebularis (Batsch) P. Kumm, which was collected from coniferous forest of northeast China in our previous work. The structure of longibrachiamide A ( 1 ) was determined by its NMR and ESI-MS/MS data, the absolute configuration of 1 was further determined by Marfey's analyses. And the complete NMR data of 2 – 4 were also reported for the first time. The similar CD spectra of 1 – 4 showed that they all had mixed 3 10 -/α-helical conformations. Compounds 1 – 4 showed strong cytotoxicities against BV2, A549 and MCF-7 cells, and also showed moderate inhibitory effects against the tested Gram-positive bacteria, including MRSA T144 and VRE-10. Graphical

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CATALYSIS LETTERS · 2014 ·Vol. 145 ·期 4 ·1000-1007 · IF 2.291

3-Aminopropyl-triethoxysilane Functionalized Graphene Oxide: A Highly Efficient and Recyclable Catalyst for Knoevenagel Condensation

Huang Jie,Ding Shunmin,Xiao Weiming,Peng Yadan,Deng Shengjun,Zhang Ning

Abstract A solid base catalyst has been prepared by covalent functionalization of graphene oxide with 3-aminopropyl-triethoxysilane. The catalyst exhibits a superior catalytic performance in Knoevenagel condensation (over 90 % yield and at least seven times reusability), and is applicable to a wide range of substrates. Graphical Abstract

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CHEMICAL ENGINEERING JOURNAL · 2025 · IF 13.2

PVA-stabilized La(OH)3-Fe2O3 composites with unparalleled cycling stability for sustainable phosphate recovery

Haotian Hao,Yao Zhang,Shuo Xu,Zihao Wang,Yili Wang,Shan Wang,Baoyou Shi

Enriching low-concentration phosphorus in water is prerequisite for phosphorus recovery. In this study, a polyvinyl alcohol (PVA)-assisted high-temperature stabilization method was developed to synthesize a magnetically recoverable La(OH) 3 -Fe 2 O 3 composite, designated as PMLH, via stable crosslinking. Compared with MLH-1, a conventionally synthesized La(OH) 3 /Fe 2 O 3 composite, PMLH-1 (La/Fe molar ratio = 1:1) exhibited 31.77 % more La(OH) 3 adsorption sites and maintained 2.32 times higher phosphate adsorption capacity after 10 reuse cycles. The optimal synthesis conditions were determined as calcination temperature of 150 °C, PVA dosage of 0.375 %, and La-to-Fe molar ratio of 1.5. Structural characterization revealed that PMLH-1.5 consisted of rod-like La(OH) 3 and irregular γ-Fe 2 O 3 tightly bonded via PVA bridging. The composite demonstrated a maximum phosphate adsorption capacity of 79.51 mg P/g, reaching equilibrium within 16 h at 0.5 g/L dosage. The saturated adsorption remained stable across pH 3–9. While coexisting NO 3 − and humic acid showed negligible effects, Mg 2+ , Cl − , SO 4 2− and HCO 3 − reduced adsorption by 10–20 %, whereas Ca 2+ significantly enhanced phosphate uptake. Notably, PMLH-1.5 exhibited exceptional practical performance, exceeding its theoretical saturation capacity by 20 % with prolonged adsorption in real water matrices. Efficient desorption (4 h) was achieved using 2.5 M NaOH/1.875 M NaCl mixed solution. The PMLH-1.5 demonstrated remarkable stability across 40 consecutive adsorption-desorption cycles using actual water samples, consistently meeting discharge standards for 13–14 full cycles. This performance established a new reference point for cyclic durability assessments in water treatment research. Sequential desorption in the same desorbent progressively concentrated phosphorus from 0 to 26.69 mg/L, enabling effective low-concentration phosphate enrichment. Economic analysis confirmed that PMLH-1.5 exhibits a competitive chemical cost, ranging from 3.28 to 5.26 CNY/mol P (0.46 to 0.74 US $/mol P).

CAS / MDL: 1309-37-1
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INORGANIC CHEMISTRY COMMUNICATIONS · 2025 · IF 5.4

Narrow-band red-emitting Li6Y1-x(BO3)3:xEu3+ phosphors with high R9 for WLEDs

Zhihao Jiang,Zihao Han,Jianwei Dao,Tiqun Wei,Zhenglin Jiang,Liang Yang

Narrowband red-emitting phosphors excited by near-ultraviolet (near-UV) light can significantly improve the R 9 and are promising for white light-emitting diodes (WLEDs). In this work, Li 6 Y 1-x (BO 3 ) 3 :xEu 3+ is first reported as a novel narrowband red phosphor, which exhibits a high R 9 value (83.8) under near-UV chip excitation for fabricating WLEDs with high color rendering index (CRI). X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) confirmed that Eu 3+ successfully partially substituted Y 3+ in the Li 6 Y(BO 3 ) 3 lattice, and all samples maintained a monoclinic P 2 1 /c structure without impurity phases. Under 396 nm near-UV excitation, Li 6 Y 1-x (BO 3 ) 3 :xEu 3+ phosphors showed intense red emission at 616 nm (attributed to the Eu 3+ 5 D 0  →  7 F 2 transition) with a full width at half maximum (FWHM = 4.8 nm), and this narrowband feature directly contributes to the improved R 9 . The optimum Eu 3+ doping concentration was 0.07; at this concentration, the red-orange ratio (the intensity ratio of 5 D 0  →  7 F 2 to 5 D 0  →  7 F 1 transitions) reached a maximum value of 4.46, indicating Eu 3+ is in a low-symmetry crystal field with high red emission purity. The luminescent intensity at 423 K remained 68.9 % of that at room temperature, with an activation energy of 0.186 eV, demonstrating excellent high-temperature stability. When the optimal phosphor was mixed with commercial BaMgAl 10 O 17 :Eu 2+ blue and (Ba, Sr) 2 SiO 4 :Eu 2+ green phosphors and packaged on a 395–400 nm chip, the fabricated WLED exhibited a high CRI (R a  = 87) and a suitable correlated color temperature (CCT = 5753 K). The results demonstrate that Li 6 Y(BO 3 ) 3 :Eu 3+ is a very promising red phosphor candidate for high-CRI solid-state lighting

CAS / MDL: 1308-96-9
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APPLIED SURFACE SCIENCE · 2019 · IF 5.155

5LiFe0.9Mn0.1PO4∙4Li3V2(PO4)3/C composites as high capacity cathode materials for lithium-ion batteries

Wei Zhao,Xunhui Xiong,Yingbang Yao,Bo Liang,Ye Fan,Shengguo Lu,Tao Tao

The construction of high capacity cathode materials consisting of two active components, LiFe x Mn 1-x PO 4 and Li 3 V 2 (PO 4 ) 3 , is rarely reported. Herein, 5LiFe 0.9 Mn 0.1 PO 4 ∙4Li 3 V 2 (PO 4 ) 3 /C (LFMVP/C) composites are synthesized by a simple two-step process, including ball milling and heat-treatment. The electrochemical reactivity of the composites with lithium is evaluated. The cathode assembled with LFMVP/C shows better electrochemical performance than that of the single active component (LiFePO 4 , LiMnPO 4, or Li 3 V 2 (PO 4 ) 3 ) during charging and discharging in the potential range of 2.4 and 4.8 V. It delivers the specific capacities of 195, 173, and 158 mAh∙g −1 at 0.1C, 0.5C, and 2C, and retains 88% of the initial discharge capacity after 100 cycles at 0.1 C. Compared with the single active component (LiFePO 4 , LiMnPO 4, or Li 3 V 2 (PO 4 ) 3 ), the lithium-ion diffusion coefficient of the composite composed of two active components (LFMVP/C) is higher.

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Journal of Materials Chemistry A · 2022 ·Vol. 10 ·期 19 ·10625-10637 · IF 14.511

3D porous spheroidal Na4Mn0.9Ce0.1V(PO4)3@CeO2/C cathode for high-energy Na ion batteries

Kun Wang,Xiaobing Huang,Tao Zhou,Dan Sun,Haiyan Wang,Zhi Zhang

The NASICON-type Na4MnV(PO4)3 (NMVP) possesses potential as a cathode material in SIBs, and is known for its stable 3D Na+ superconductive framework, high voltage platform, and relatively low cost and toxicity. Nevertheless, the intrinsic poor electronic conductivity and Jahn–Teller effect from Mn3+ during cycling limit its further application. Herein, to address such issues, a well-designed 3D porous spheroidal Ce3+-doped NMVP@CeO2/C cathode was constructed via a simple spraying drying-assisted route. As proved, the synergistic effect of Ce3+ doping in the crystal framework and CeO2 surface coating was achieved simultaneously, which greatly improved the electronic conductivity, facilitated the ion diffusion transfer and stabilized the crystalline structure. As a result, the as-prepared sample delivered superior discharge performance (50.3 mA h g−1 at 50C) and long circular life (91.0 mA h g−1 after 2000 cycles at 5C with 86.7% capacity retention). Furthermore, the reversible biphasic reaction for cathodes was confirmed by Galvanostatic intermittent titration technique (GITT) and ex situ XRD. The DFT calculation revealed the influence of Ce3+-doping on the crystalline framework and electrochemical properties. Finally, the optimized NMVP cathode also showed great potential for practical utilization through the successful assembly of full cells.

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AQUATIC TOXICOLOGY · 2024 · IF 4.1

Toxicity comparison of benzophenone-3 and its metabolite benzophenone-8 in different tissues of zebrafish

Yonghua Wang,Yujia Shang,Xiaodan Liu,Xi Chen,Guanhua Xu,Guanghua Lu

Benzophenone-3 (BP-3) is a commonly used ultraviolet absorber that has the potential to accumulate in organisms, leading to toxicity. Benzophenone-8 (BP-8) is one of the major metabolites of BP-3. In this study, zebrafish were exposed to different concentrations of BP-3 and BP-8 (1 μg/L, 30 μg/L, and 300 μg/L) to investigate their accumulation and toxic effects in various tissues, including zebrafish brain, gut, and liver. The analysis focused on neurotoxicity, oxidative damage, inflammation, and gene expressions. The results showed that both BP-3 and BP-8 accumulated in the tissues, with the highest concentration observed in the gut, followed by the liver and brain. BP-8 exhibited a stronger ability to accumulate. In the brain, exposure to 1 μg/L of BP-3 and BP-8 promoted cortisol production, while higher exposures (30 μg/L and 300 μg/L) inhibited acetylcholinesterase activity and suppressed cortisol production. In the gut, both BP-3 and BP-8 exposures disrupted oxidative stress, inflammatory immunity, and apoptosis functions. In the liver, BP-3 and BP-8 affected hepatic metabolism, oxidative stress, apoptosis, and inflammatory immunity. Comparing gene expression in the brain, gut, and liver, it was found that BP-3 and BP-8 had a lower effect on gene expression in the brain, while the effect on the gut and liver was significantly higher. BP-8 generally had a higher effect than BP-3, which aligns with the observed accumulation pattern. These findings provide valuable insights for the risk assessment of BP-3 and BP-8 in the aquatic environment.

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SURFACE & COATINGS TECHNOLOGY · 2024 · IF 5.3

One-step in-situ construction of Mg0.5Ti2(PO4)3 coating and cation doped modified LiNi0.5Mn1.5O4

Dongjia Li,Bo Xiao,Xinyi Dai,Chao Wang,Yawei Wei,Haijun Chen,Yi Mai,Fuzhong Wu,Jiexi Wang

Amid the fast growth of lithium-ion batteries, LiNi 0.5 Mn 1.5 O 4 (LNMO) with a 4.7 V working voltage and cost advantages has gained significant attention. The instability of LNMO structure during high-voltage cycling leads to significant side reactions with the electrolyte, hindering its commercial development. Our study introduces a co-crystallization calcination strategy to enhance the optimization of LNMO. This study utilized a straightforward wet chemistry approach to combine the precursor of NASICON-type solid electrolyte Mg 0.5 Ti 2 (PO 4 ) 3 (MTP) with the precursor of LNMO. Subsequently, a MTP coating was formed in-situ on the surface of LNMO through a single-step calcination process. Co-crystallization and calcination processes limit LNMO particle secondary growth, shorten Li + diffusion path , achieve Mg 2+ and Ti 4+ co-doping, enhance structural stability , and result in triple modification, leading to a significant improvement in electrochemical performance . Among them, LNMO with a 1 % molar ratio modified by MTP reaches 81.7 % of the initial capacity after 500 cycles at room temperature and 84.3 % after 180 cycles at 55 °C. Under identical conditions, unmodified samples have 39.3 % and 76.3 %, respectively. Our research explores a novel application of NASICON-type solid electrolytes in modifying LNMO cathode material .

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SOLAR ENERGY · 2021 · IF 5.742

Defect passivation grain boundaries using 3-aminopropyltrimethoxysilane for highly efficient and stable perovskite solar cells

Ronghong Zheng,Shuangshuang Zhao,Hua Zhang,Haoyue Li,Jia Zhuang,Xingchong Liu,Haimin Li,Hanyu Wang

The defects of grain boundaries and film surface are harmful to the efficiency and stability of perovskite solar cells (PSCs). Defect passivation is an effective strategy to improve the performance of PSCs. In this work, a silane coupling agent 3-aminopropyltrimethoxysilane (APMS) was used as an additive of perovskite light-absorbing layer to passivate defects, thereby significantly improving charge transport, reducing charge recombination and improving device performance. The amino group in APMS can not only form a coordinate bond with the uncoordinated Pb in the perovskite, but also form a hydrogen bond with I (N-H⋯I). The crystallinity and uniformity of perovskite grains were improved obviously. Therefore, the addition of APMS greatly reduces the defects of perovskite and the power conversion efficiency (PCE) increased from 18.85% to 20.72% with less hysteresis. Furthermore, a proper carbon chain can be hydrophobic to improve the moisture stability of the perovskite. The PCE of the device remains 60% of the initial device after being placed at a humidity of 50–60% for 400 h. Therefore, this work proves that the use of silane coupling agents as additives is a promising strategy to achieve efficiency and stable PSCs.

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JOURNAL OF THE AMERICAN CERAMIC SOCIETY · 2023 ·Vol. 106 ·期 5 ·2963-2971 · IF 3.9

Electrostatic energy storage performances of La(Ni2/3Ta1/3)O3-modified Na0.5Bi0.5TiO3 lead-free ceramics

Nan Weng,Ji Zhang,Jiajia Wang,Tianze Pan,Jing Wang,Yaojin Wang

Ceramic capacitors with high electrostatic energy storage performances have captured much research interest in latest years. Sodium bismuth titanate (Na 0.5 Bi 0.5 TiO 3 )-based ferroelectric ceramics show great potential due to their environment-friendly composition, high polarization, and excellent relaxor properties. However, the nonergodic relaxor state of Na 0.5 Bi 0.5 TiO 3 -based ceramics hampers the decrement of remanent polarization, leading to poor energy storage performance. Herein, the (1 − x )Na 0.5 Bi 0.5 TiO 3 – x La(Ni 2/3 Ta 1/3 )O 3 ceramics were designed to generate the transformation between nonergodic and ergodic relaxor state. As a result, the ceramics exhibit improved dielectric relaxation, slim polarization–electric field loops, and flattened current–electric field curves due to highly dynamic polar nanoregions. Particularly, the 0.85Na 0.5 Bi 0.5 TiO 3 –0.15La(Ni 2/3 Ta 1/3 )O 3 ceramics show large breakdown electric field E b (345 kV/cm), high recoverable energy density W rec (3.6 J/cm 3 ), and efficiency η (80.6%), revealing potential applications in electrostatic energy storage.

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INTEGRATED FERROELECTRICS · 2021 · IF 0.836

Realizing Hybrid Ion Storage of NASICON-Structured Na3V2(PO4)3 Prepared by Microwave Irradiation Route

Ji Yan,Zhen Li,Xiao-Kai Ma,Xin-Bo Chang,Fu-Jun Liu,Yong Zhang,Li-Zhen Wang

NASICON Na3V2(PO4)3 was investigated as cathode material in hybrid ion batteries using Li as counter and LiPF6 as electrolyte. The highly efficient and homogeneous heating merits of microwave irradiation facilitates the Na3V2(PO4)3 achieving excellent crystal structure, uniform carbon coating, as well as ideal particle size. After microwave irradiation, a specific capacity of 96.5 mAh g−1 is obtained for the first intercalation of lithium ion into Na3V2(PO4)3 at 0.1 C rate. For long-term cycling stability, the capacity retention reaches 84.4% at 5 C rate after 500 cycles. The unique intercalation/extraction characteristic promises Na3V2(PO4)3 an ideal candidate material for next-generation hybrid ion storage system.

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