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JOURNAL OF MATERIALS SCIENCE · 2022 ·Vol. 57 ·期 34 ·16541-16553 · IF 4.682

A curing agent for epoxy resin based on microencapsulation of 1-butylimidazole

Zhang Binghong,Ma Aijie,Li Jiaoyang,Xiao Siyu,Li Chunmei,Zhao Weifeng,Zhang Gai,Zhang Hongli

An efficient and economical strategy for rapid microencapsulation of 1-butylimidazole (1-BMI) was developed. The strategy is based on the thiol-yne click reaction of trimethylolpropane tris(3-mercaptopropionate) and 1,7-octadiyne in oil-in-water emulsion. The thiol-yne click reaction is not only green and efficient, but also improves the cross-linking density of shell. Thus, the obtained shell prevents the leakage of curing agent and prolongs the storage period of EP/MCs system. The whole process of preparing 1BMI-MCs only took 40 min. Moreover, the effects of stirring speed and the ratio of 1BMI on the size and core content of microcapsules (MCs) were investigated. Results demonstrated that the optimal particle size was about 10.8 μm, and the maximum content of 1BMI in MCs was 33% corresponding to 60% 1BMI in oil phase. Afterward, the 1BMI MCs were used as latent curing agent (LCA) for epoxy resin (EP). In the curing reaction of the epoxy resin, the 1BMI-MCs exhibited a delayed kinetic behavior compared to pure 1BMI. Furthermore, the E-51/MCs system had a storage term of 16 weeks. The shell material not only had no effect on curing effect of E-51, but also toughen the cured EP systems. This paper provided a promising method for long-term storage of LCA.

研究领域: 材料科学 · 化学工程
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INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE · 2025 ·Vol. 55 ·期 3 ·1-14 · IF 5.8

Aquaporin‑1 regulates microglial polarization and inflammatory response in traumatic brain injury

Yixuan Ma,Yimin Huang,Xuyang Liu,Liwu Jiao,Hongtao Zhu,Zhiye Chen,Zhuojin Wu,Yuanzhong Shen,Kehan Lin,Feng Hu,Kai Shu

The present study investigated the mechanisms by which aquaporin 1 (AQP1) influences microglial polarization and neuroinflammatory processes in traumatic brain injury (TBI). A model of TBI was generated in AQP1‑knockout mice to assess the impact of AQP1 deletion on inflammatory cytokine release, neuronal damage and cognitive function. Immunofluorescence, reverse transcription‑quantitative PCR, western blotting and enzyme‑linked immunosorbent assay were employed to evaluate pro‑inflammatory and anti‑inflammatory markers. Behavioral assessments, including the Barnes maze, were performed to determine cognitive outcomes. Moreover, AQP1 knockout inhibited the activation of inflammation‑related signaling pathways, including nuclear factor‑κB, Janus kinase/signal transducer and activator of transcription, phosphoinositide 3‑kinase/protein kinase B and extracellular signal‑regulated kinase/mitogen‑activated protein kinase pathways. Further studies indicated that the AQP1 inhibitor m‑phenylenediacrylic acid demonstrated significant neuroprotective effects in a mouse model of TBI. These findings suggested that AQP1 may be essential in post‑TBI inflammatory responses and neuronal injury, establishing a theoretical foundation for future therapies aimed at AQP1.

CAS / MDL: 314-13-6
研究领域: 神经科学 · 炎症生物学 · 分子医学
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FUEL · 2018 · IF 4.908

A highly active bifunctional solid acid for di(1-naphthyl)methane hydroconversion

Qing-Qing Teng,Xian-Yong Wei,Yi-Bing Sun,Sheng-Kang Wang,Jing-Hui Lv,Zhan-Ku Li,Zhong-Qiu Liu,Zhi-Min Zong

Catalysts trifloromethanesulfonic acid (TFMSA)/treated attapulgite powder (TAP), Ni/TAP, and Ni-TFMSA/TAP with different Ni and TFMSA loadings were prepared. The typical catalysts were characterized with multiple instruments and used for catalyzing hydroconversion of di(1-naphthyl)methane (DNM), which was used as a coal-related model compound. The suitable loadings of Ni and TFMSA in Ni-TFMSA/TAP were determined to be 28.6% of Ni and 33% of TFMSA. Under optimal reaction conditions of 5 MPa of initial hydrogen pressure, 240 °C, and 4 h over Ni-TFMSA/TAP, DNM was completely converted, producing decalin and 1-methyldecalin as the main products. The result suggests that Ni-TFMSA/TAP is highly active for both cleaving the C ar -C alk bond in DNM and hydrogenating the resulting naphthalene and 1-methylnaphthalene under mild conditions. Based on the identification of reaction products, the catalytic mechanism for DNM hydroconversion was discussed.

研究领域: 催化化学 · 能源化学
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RADIATION PHYSICS AND CHEMISTRY · 2025 · IF 3.3

Radiolysis of diamide phenanthroline in 1-octanol: From the insights into transient processes to a versatile strategy to enhance the radiation-resistance

Hanqin Weng,Baoying Zhang,Yizhi Chen,Shinichi Yamashita,Yusa Muroya,Hao Yu,Xinrui Zhang,Xiaofan Yang,Weiqun Shi

The ligand of 2,9-Diamide-1,10-phenanthroline (DAPhen), developed for group actinide separation in the past decade, showed excellent extraction and separation performance for various actinides from trivalent lanthanides. However, its radiolysis mechanism remains unclear, restricting its application. Mechanism for the radiolysis of three different DAPhen in 1-octanol was studied by pulse radiolysis, of which the results demonstrated that reductive degradation was the main route of their radiolysis in 1-octanol. Solvated electrons (e sol − ), and α-hydroxyoctyl radicals have been recognized as the most important transient species responsible for DAPhen radiolysis. Rate constants for the reactions of e sol − with N,N′ -diethyl- N,N′ -ditethyl-2,9-diamide-1,10-phenanthroline (Et–Et-DAPhen, EED), N,N′ -dioctyl- N,N′ -ditoctlyl-2,9-diamide-1,10-phenanthroline (Oct-Oct-DAPhen, OOD), and N,N′ -diethyl- N,N′ -ditolyl-2,9-diamide-1,10-phenanthroline (Et-Tol-DAPhen, ETD) were estimated to be 1.9 × 10 9 , 2.3 × 10 9 , and 1.5 × 10 9  L mol −1  s −1 , respectively. Those of α-hydroxyoctyl radicals with EED, OOD, and ETD were approximately 1.1 × 10 8 , 2.1 × 10 8 , and 2.7 × 10 8  L mol −1  s −1 , respectively. The studied DAPhen exhibited high reactivity with e sol − , and α-hydroxyoctyl radicals in 1-octanol, resulting in their vulnerability under irradiation. A versatile strategy was accordingly proposed to enhance their radiation stability based on the insights into transient processes of DAPhen radiolysis. If the HNO 3 -equilibrated organic phase was saturated with nitrous oxide (N 2 O), the reductive species responsible for DAPhen degradation would be scavenged. As a consequence, the radiation-resistance of DAPhen was significantly improved because the key elementary reaction of radiolysis was inhibited by the synergetic effect of N 2 O and HNO 3 .

CAS / MDL: 111-87-5
研究领域: 放射化学 · 配体设计 · 核化学与技术
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JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY · 2024 · IF 4.5

Engineering synergistic liposomes against ovarian cancer via concurrent targeting of myeloid cell leukemia-1(MCL-1) and glutamate-cystine antiporter (SLC7A11)

Yaru Li,Qian Yang,Lanlan Fan,Fang Liu,Yaqi Shang,Baoxin Zhang,Zheng Wang,Yanjun Zhao

Ovarian cancers (OC) often resist current standard chemotherapy because of the cancer heterogeneity and over-expression of an anti-apoptotic protein, myeloid cell leukemia-1 (MCL-1). The heterogeneous OC shows impaired redox homeostasis and relies heavily on glutathione peroxidase 4 to eliminate toxic lipid peroxides. Therefore, integrated apoptosis and ferroptosis therapy is promising for OC management. The current work reports a liposomal nanosystem for apoptotic and ferroptotic OC therapy. Simvastatin (Sim) and vorinostat (Saha) were selected as the pleiotropic model drugs. The successive release of Saha and Sim from liposomes enabled the sequential amplification of MCL-1 by Saha, and then MCL-1 inhibition by Sim. Such a strategy could potently induce apoptosis in a human OC cell line (SKOV3), as indicated by increased intracellular cytochrome c concentration, caspase 3/9 activity, and the extent of apoptosis. Besides, Saha played multiple roles in cell death. It could induce cell cycle arrest at the G 2 /M phase and apoptosis. Saha also inhibited the glutamate-cystine transporter (SLC7A11) and provoked ferroptosis, which was corroborated by the depletion of glutathione, reduced nicotinamide adenine dinucleotide phosphate, and boost of lipid peroxides and malondialdehyde in SKOV3 cells. The current work integrated the “sequential amplification and inhibition of MCL-1 target” concept with combinational apoptosis and ferroptosis OC therapy, which might offer a new approach for managing resistant OC and other malignant diseases.

研究领域: 肿瘤学 · 药学 · 细胞生物学 · 纳米技术
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ACTA PHARMACOLOGICA SINICA · 2025 · IF 8.4

Dehydrotrametenolic acid methyl ester, a triterpenoid of Poria cocos, alleviates non-alcoholic steatohepatitis by suppressing NLRP3 inflammasome activation via targeting Caspase-1 in mice

Xia Ling-yan,Yu Nai-rong,Huang Su-ling,Qu Hui,Qin Li,Zhao Qin-shi,Leng Ying

Non-alcoholic steatohepatitis (NASH) has emerged as a prevalent chronic liver disease with a huge unmet clinical need. A few studies have reported the beneficial effects of Poria cocos Wolf ( P. cocos ) extract on NASH mice, but the active components were still unknown. In this study we investigated the therapeutic effects of dehydrotrametenolic acid methyl ester (ZQS5029-1), a lanosterol-7,9(11)-diene triterpenes in P. cocos , in a high-fat diet plus CCl 4 induced murine NASH model and a GAN diet induced ob/ob murine NASH model. The NASH mice were treated with ZQS5029-1 (75 mg·kg –1 ·d –1 , i.g.) for 6 and 8 weeks, respectively. We showed that ZQS5029-1 treatment markedly relieved liver injury, inflammation and fibrosis in both the murine NASH models. We found that ZQS5029-1 treatment significantly suppressed hepatic NOD-, LRR-, and pyrin domain-containing protein 3 (NLRP3) inflammasome activation in both the NASH murine models, and blocked lipopolysaccharides (LPS)+adenosine 5’-triphosphate (ATP)/Nigericin-induced NLRP3 inflammasome activation in bone marrow-derived macrophages (BMDMs) and Kupffer cells in vitro. We demonstrated that ZQS5029-1 directly bound to the H236 residue of mouse Caspase-1, thereby inhibiting NLRP3 inflammasome activation. The effects of ZQS5029-1 on macrophage-hepatocyte/HSC crosstalk were analyzed using the supernatants from macrophages preconditioned with LPS + ATP introduced into hepatocytes and hepatic stellate cells (HSCs). We found that the conditioned medium from the BMDMs induced injury and death, as well as lipid accumulation in hepatocytes, and activation of HSCs; these effects were blocked by conditioned medium from BMDMs treated with ZQS5029-1. Moreover, the protective effects of ZQS5029-1 on hepatocytes and HSCs were eliminated by H236A-mutation of Caspase-1. We conclude that ZQS5029-1 is a promising lead compound for the treatment of NASH by inhibiting NLRP3 inflammasome activation through targeting Caspase-1 and regulating the macrophage-hepatocyte/HSC crosstalk.

CAS / MDL: 56-23-5
研究领域: 药理学 · 肝脏病学 · 免疫学
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RADIOCHIMICA ACTA · 2022 ·Vol. 111 ·期 1 ·63-71 · IF 2.083

1-aza-18-crown-6 ether tailored graphene oxide for Cs(I) removal from wastewater

Peng Liu,Zhuang Shen,Jiaxian Cheng,Zhen Han,Wenda Xu,Mingbo Ji,Fuqiu Ma

Due to the relative abundance, long half-life and high mobility of radioactive cesium (Cs), new adsorbents are urgently needed to treat Cs to ensure public health. In this study, a graphene oxide (GO) based adsorbent for Cs(I) adsorption was prepared by 1-aza-18-crown-6 ether modification. XRD, FT-IR, XPS and SEM results showed that the properties of 1-aza-18-crown 6 ether modified GO (18C6-GO) changed dramatically compared with that of raw graphite. The adsorption properties of 18C6-GO for Cs(I) were studied by batch static adsorption experiments. The results showed that the adsorption equilibrium time of 18C6-GO was 20 h. Kinetic study revealed that the adsorption rate of Cs(I) conformed to pseudo-second-order kinetic model. Langmuir adsorption isotherm simulation indicated that the adsorption arises at homogeneous adsorption sites on 18C6-GO. Therefore, crown ether modified GO may have implications for the treatment of wastewater.

研究领域: 环境科学 · 材料科学 · 化学工程
✓ 已验证 DOI 高影响因子
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ACS Nano · 2025 · IF 16

Polyhedral Polymeric Microparticles with Interwoven 1 nm Gyroid Pores for Precise Adsorption and Nanoconfined Degradation

Hairui Huang,Hanyu Wu,Yizhou Zhang,Xunda Feng

Molecular-scale adsorption, catalysis, and separation demand nanoporous materials with high permeability, extensive surface areas, and pronounced nanoconfined effects. Fabricating polymeric particles with 3-D interwoven pores of ∼1 nm potentially addresses these needs. However, significant challenges remain in controlling their pore interconnectivity, uniformity, and achieving faceted particle shapes. Herein we present facile fabrication of polyhedral particles possessing interpenetrating 1 nm pores by suspension polymerization of double-gyroid (DG) liquid crystalline droplets. Mechanical stirring of the disordered phase at elevated temperatures, followed by undercooling, leads to the emulsification of DG droplets, as confirmed by synchrotron small-angle X-ray scattering (SAXS). UV-induced cross-linking of the DG droplets preserves the ordered network of 1 nm pores, as characterized by SAXS and microscopy. Intriguingly, due to the elasticity induced by the Ia3̅d periodicities, these particles adopt polyhedral shapes to avoid the elastic energy penalty associated with conventional sphericity. We demonstrate that these faceted particles, featuring 1 nm pores and efficient packing, enable rapid, size-exclusive adsorption and nanoconfined degradation of organic pollutants, driven by their 3-D permeability, high surface area, and enhanced nanoconfinement effects.

研究领域: 材料科学 · 环境科学 · 化学工程
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CHINESE JOURNAL OF CATALYSIS · 2025 · IF 17.7

Dimethoxymethane carbonylation and disproportionation over extra-large pore zeolite ZEO-1: Reaction network and mechanism

Shaolei Gao,Peng Lu,Liang Qi,Yingli Wang,Hua Li,Mao Ye,Valentin Valtchev,Alexis T. Bell,Zhongmin Liu

Methyl methoxyacetate (MMAc) and methyl formate (MF) can be produced directly by heterogeneous zeolite-catalyzed carbonylation and disproportionation of dimethoxymethane (DMM), with near 100% selectivity for each process. Despite continuous research efforts, the insight into the reaction mechanism and kinetics theory are still in their nascent stage. In this study, ZEO-1 material, a zeolite with up to now the largest cages comprising 16×16-MRs, 16×12-MRs, and 12×12-MRs, was explored for DMM carbonylation and disproportionation reactions. The rate of MMAc formation based on accessible Brönsted acid sites is 2.5 times higher for ZEO-1 (Si/Al = 21) relative to the previously investigated FAU (Si/Al = 15), indicating the positive effect of spatial separation of active sites in ZEO-1 on catalytic activity. A higher MF formation rate is also observed over ZEO-1 with lower activation energy (79.94 vs. 95.19 kJ/mol) compared with FAU (Si/Al = 30). Two types of active sites are proposed within ZEO-1 zeolite: Site 1 located in large cages formed by 16×16-MRs and 16×12-MRs, which is active predominantly for MMAc formation, and Site 2 located in smaller cages for methyl formate/dimethyl ether formation. Kinetics investigation of DMM carbonylation over ZEO-1 exhibit a first-order dependence on CO partial pressure and a slightly inverse-order dependence on DMM partial pressure. The DMM disproportionation is nearly first-order dependence on DMM partial pressure, while it reveals a strongly inverse dependence with increasing CO partial pressure. Furthermore, ZEO-1 exhibits good catalytic stability, and almost no deactivation is observed during the more than 70 h test with high carbonylation selectivity of above 89%, due to the well-enhanced diffusion property demonstrated by intelligent-gravimetric analysis.

CAS / MDL: 109-87-5
研究领域: 化学工程 · 催化科学
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

PIM-1-based membranes mediated with CO2-philic MXene nanosheets for superior CO2/N2 separation

Kaifang Wang,Danlin Chen,Jiali Tang,Zihao Hong,Zhongtai Zhu,Ziyi Yuan,Zhihong Lin,Yuqi Liu,Raphael Semiat,Xuezhong He

Membrane gas separation technologies have emerged as highly prospective avenues for the selective separation of CO 2 . In this research, a novel array of mixed-matrix membranes (MMMs) was engineered, integrating two-dimensional nanosheets of MXene, specifically Ti 3 C 2 T x , into polymers of intrinsic microporosity (PIMs) to selectively separate CO 2 from N 2 . The inclusion of Ti 3 C 2 T x nanosheets, rich in polar functional groups, significantly increases the affinity between CO 2 molecules and the fabricated MMMs. Additionally, the precise modulation of the molecular diffusion channels for CO 2 and N 2 is achievable due to the interlayer spacing between MXene layers (∼0.35 nm) within the PIM-1 matrix. This innovation is predicated on the synergistic effect of solution-diffusion and molecular sieving mechanisms that underpin the gas separation process, leading to a marked improvement in both selectivity for CO 2 over N 2 and the permeability of CO 2 . Among the series, the MMMs with a 0.5 wt% MXene display exceptional separation efficiency, achieving a CO 2 permeability of 12475.3 barrer and a CO 2 /N 2 selectivity of 32.7. Notably, all the PIM-1/MXene membranes prepared with different compositions in this study exceed the Robeson upper bound defined in 2019, indicating their substantial promise for CO 2 separation and capture in industrial applications.

CAS / MDL: 584-08-7 77-08-7
研究领域: 材料科学 · 环境工程 · 化学工程
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Molecular Catalysis · 2024 · IF 3.9

Grafting EDTA in UiO-66 to modulate the microenvironment of Rh for 1-hexene Hydroformylation

Yuhao Yang,Minghui Tan,Hailun Geng,Xiujuan Gao,Yisheng Tan,Qingde Zhang

Oriented designing the microenvironment of catalytic sites is essential for understanding catalytic processes. In this work, EDTA was first grafted in UiO-66 and then chelated Rh to obtain an efficient catalyst for 1-hexene hydroformylation reaction. EDTA not only served as a chelation site for Rh immobilization in UiO-66, but also markedly influenced the structure and properties of Rh/UiO-66. The incorporation of EDTA reduced the micropore content and suppressed the formation of heavy products. Moreover, the grafted EDTA regulated the electronic state of Rh effectively to improve the CO and propene adsorption, thus constructing an appropriate microenvironment for hydroformylation. Therefore, EDTA-modified Rh/U-E catalyst exhibited higher aldehydes yield, TOF and stability than Rh/U without EDTA. The dual role of EDTA in anchoring Rh sites and modulating the microenvironment for hydroformylation provides more prospects for designing customized MOFs-based catalysts.

研究领域: 催化化学 · 材料科学
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Communications Biology · 2024 ·Vol. 7 ·期 1 ·1-13 · IF 5.2

High temperature and humidity in the environment disrupt bile acid metabolism, the gut microbiome, and GLP-1 secretion in mice

Chen Song,Hu Zongren,Tang Jianbang,Zhu Haipeng,Zheng Yuhua,Xiao Jiedong,Xu Youhua,Wang Yao,Luo Yi,Mo Xiaoying,Wu Yalan,Guo Jianwen,Zhang Yongliang,Luo Huanhuan

High temperature and humidity in the environment are known to be associated with discomfort and disease, yet the underlying mechanisms remain unclear. We observed a decrease in plasma glucagon-like peptide-1 levels in response to high-temperature and humidity conditions. Through 16S rRNA gene sequencing, alterations in the gut microbiota composition were identified following exposure to high temperature and humidity conditions. Notably, changes in the gut microbiota have been implicated in bile acid synthesis. Further analysis revealed a decrease in lithocholic acid levels in high-temperature and humidity conditions. Subsequent in vitro experiments demonstrated that lithocholic acid increases glucagon-like peptide-1 secretion in NCI-H716 cells. Proteomic analysis indicated upregulation of farnesoid X receptor expression in the ileum. In vitro experiments revealed that the combination of lithocholic acid with farnesoid X receptor inhibitors resulted in a significant increase in GLP-1 levels compared to lithocholic acid alone. In this study, we elucidate the mechanism by which reduced lithocholic acid suppresses glucagon-like peptide 1 via farnesoid X receptor activation under high-temperature and humidity condition.

研究领域: 生理学 · 微生物学 · 内分泌学 · 分子生物学
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