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MOLECULES · 2025 ·Vol. 30 ·期 13 ·2691 · IF 4.6

Highly Engineered Cr-In/H-SSZ-39 Catalyst for Enhanced Performance in CH4-SCR of NOx

Jiuhu Zhao,Jingjing Jiang,Guanyu Chen,Meng Wang,Xiaoyuan Zuo,Yanjiao Bi,Rongshu Zhu

The selective catalytic reduction of NOxwith CH4(CH4-SCR) holds the potential to simultaneously abate harmful NOxand CH4greenhouse gases. In this study, a series of bimetallic M-In/H-SSZ-39 catalysts (where M represents Cr, Co, Ce, and Fe) were prepared via an ion exchange method and subsequently evaluated for their CH4-SCR activity. The influences of the preparation parameters, including the metal ion concentration and calcination temperature, as well as the operating conditions, such as the CH4/NO ratio, O2concentration, water vapor content, and gas hourly space velocity (GHSV), on the catalytic activity of the optimal Cr-In/H-SSZ-39 catalyst were meticulously examined. The results revealed that the Cr-In/H-SSZ-39 catalyst exhibited peak CH4-SCR catalytic performance when the Cr(NO3)3concentration was 0.0075 M, the In(NO3)3concentration was 0.066 M, and the calcination temperature was 500 °C. Under optimal operating conditions, namely GHSV of 10,000 h−1, 400 ppm NO, 800 ppm CH4, 15 vol% O2, and 6 vol% H2O, the NOxconversion rate reached 93.4%. To shed light on the excellent performance of Cr-In/H-SSZ-39 under humid conditions, a comparative analysis of the crystalline phase, chemical composition, pore structure, surface chemical state, surface acidity, and redox properties of Cr-In/H-SSZ-39 and In/H-SSZ-39 was conducted. The characterization results indicated that the incorporation of Cr into In/H-SSZ-39 enhanced its acidity and also facilitated the generation of InO+active species, which promoted the oxidation of NO and the activation of CH4, respectively. A synergistic effect was observed between Cr and In species, which significantly improved the redox properties of the catalyst. Consequently, the activated CH4could further interact with InO+to produce carbon-containing intermediates such as HCOO−, which ultimately reacted with nitrate-based intermediates to yield N2, CO2, and H2O.

CAS / MDL: 207398-97-8
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ACS Applied Polymer Materials · 2025 · IF 4.7

Flexible and Electrically Insulating MPCF/H-BN/CAB Composites with Engineered Interfaces for Superior Thermal Conductivity

Xuewei Yang,Rui Li,Yong Liu,Jian Xu,Ning Zhao

The rapid evolution of flexible wearable electronics necessitates efficient thermal management, driving the demand for materials that are not only thermally conductive but also electrically insulating and flexible. In this study, a thermal conductive composite with aligned filler structure was fabricated using catechol/tetraethylenepentamine (CAT-TEPA) surface-modified hexagonal boron nitride (h-BN) and mesophase pitch-based carbon fibers (MPCF) as fillers, and cellulose acetate butyrate (CAB) as the polymer matrix via evaporation self-assembly and hot-pressing. By optimizing the interface through CAT-TEPA modification and leveraging the long-range structural alignment of MPCF, an efficient thermal conduction network of h-BN sheets was formed. The composite containing 50 wt % total filler content (3 wt % MPCF) achieved an exceptional in-plane thermal conductivity of 21.75 W/mK, and a high volume resistivity of 1.5 × 1011 Ω·cm. Furthermore, the material demonstrated remarkable flexibility, making it a promising candidate for thermal management applications in flexible electronics.

CAS / MDL: 112-57-2 120-80-9
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CURRENT PHARMACEUTICAL DESIGN · 2022 ·Vol. 28 ·期 9 ·743-750 · IF 3.31

Effect and Mechanism of the Lenvatinib@H-MnO2-FA Drug Delivery System in Targeting Intrahepatic Cholangiocarcinoma

Ning Zhouyu,Yang Lina,Yan Xia,Wang Dan,Hua Yongqiang,Shi Weidong,Lin Junhua,Meng Zhiqiang

Background: To investigate the effects of the Lenvatinib@H-MnO2-FA administration system on the proliferation and apoptosis of Intrahepatic cholangiocarcinoma (ICC) and the underlying molecular mechanism. Materials and Methods: In this research, hollow MnO2 (H-MnO2) was synthesized via the modified Stöber method, and H-MnO2 was modified with polyethylene glycol-bis (Amine) (NH2-PEG-NH2) and folic acid (FA) to obtain H-MnO2-PEG-FA (H-MnO2-FA). Lenvatinib was coated in the hollow cavity of H-MnO2-PEG-FA to further form a nanometre drug-carrying system (Lenvatinib@H-MnO2-PEG-FA). Lenvatinib@H-MnO2-FA was characterized through transmission electron microscopy (TEM) and scanning electron microscopy (SEM). Fourier transform infrared spectroscopy (FT-IR) was used to verify that Lenvatinib was loaded on nanoparticles. Functionally, confocal laser scanning microscopy (CLSM), 2-(4-Amidinophenyl)-6-indolecarbamidine dihydrochloride (DAPI) staining, and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay were performed to determine the effect of Lenvatinib@H-MnO2-FA on the proliferation and apoptosis of ICC cells (9810 cells). Finally, the protein levels of Raf-1MEK1/2-ERK1/2 signalling pathway components were detected through Western blotting analysis. Results: We successfully synthesised a Lenvatinib@H-MnO2-PEG-FA administration system. The resulting nanomaterials had excellent biological stability and improved targeting effects. Functionally, Lenvatinib@ H-MnO2-FA inhibited the proliferation of 9810 cells. The Bcl-2 protein level was significantly downregulated, and the caspase-3 protein level was significantly upregulated, indicating that Lenvatinib@H-MnO2- PEG- FA promoted the apoptosis of 9810 cells. Mechanistically, Lenvatinib@H-MnO2-FA increased the phosphorylation levels of Raf, MEK1/2, and ERK1/2. Conclusion: H-MnO2-FA can more effectively deliver Lenvatinib to inhibit proliferation and promote apoptosis in ICC, which could be the promising drug delivery nano-vehicles for delivery drugs.

✓ 已验证 DOI PubMed 高影响因子
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RESOURCES CONSERVATION AND RECYCLING · 2021 · IF 10.204

Atomic H* enhanced electrochemical recovery towards high-value-added metallic Sb from complex mine flotation wastewater

Liming Yang,Genping Yi,Bo Wang,Penghui Shao,Yufa Feng,Yanbiao Liu,Kai Yu,Fuqiang Liu,Lingling Liu,Xubiao Luo,Shenglian Luo

Simultaneous recovery and value-added conversion of hazardous heavy metal ions from complex wastewater sources is of great significance yet challenging. Herein, we demonstrate that highly toxic antimonite Sb(III) could be effectively recovered from antimony (Sb) mine flotation wastewater and converted into high-value-added metallic Sb using a novel facile atomic H* enhanced electrochemical reduction avenue coupled with thermal reduction by H 2 gas. The high production of atomic H* generated from the electrochemical cathode with an optimum reduction potential of –1.2 V vs . Ag/AgCl, which is lower than the Sb(III) reduction potential of –1.0 V, might be attributable to the superior Sb recovery capabilities. Furthermore, the metallic Sb concentration at –1.2 V was 14.43 times greater than at –1.0 V due to the strong reductivity of atomic H*. In addition, Sb(III) removal efficiency was found to be as high as 98.52%, with a metallic Sb recovery rate of up to 1.67 mg min –1 . The efficiency of Sb(III) recovery was demonstrated throughout a wide pH range, with metallic Sb being the main product, independent of the presence of multiple coexisting ions. Economic analysis also indicated that treating Sb mine flotation wastewater per ton may yield a net profit of $40.09. This research contributes to the advancement of an atomic H* enhanced electrochemical technology for high-valued heavy metal recovery from complex heavy metal-polluted wastewater.

✓ 已验证 DOI 高影响因子
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PROGRESS IN ORGANIC COATINGS · 2020 · IF 4.469

Polyethylenimine-assisted exfoliation of h-BN in aqueous media for anticorrosive reinforcement of waterborne epoxy coating

Hongyi Shi,Weiqu Liu,Chunhua Liu,Maiping Yang,Yankun Xie,Shuo Wang,Fengyuan Zhang,Liyan Liang,Ke Pi

Herein, h-BN powders were sonicated in an aqueous solution of polyethylenimine (PEI) to simultaneously exfoliate and functionalize h-BN nanosheets with Lewis acid-base interaction. The structure and morphology of PEI modified h-BN nanosheets (PEI-BNNSs) were characterized by FTIR, TGA, AFM and TEM. The as-prepared PEI-BNNSs were served as anticorrosive nanofillers for waterborne epoxy (EP) coatings on Q235 carbon steel. The corrosion behaviors of EP and PEI-BNNSs/EP coating systems in 3.5 wt % NaCl aqueous solution were evaluated by electrochemical workstation. It is worth noting that the protection efficiency (PE) values of 1 wt % PEI-BNNSs/EP and 2 wt % PEI-BNNSs/EP coating systems are as high as 99.99 % compared to EP coating systems. Moreover, the impedance modulus (|Z| f = 0.01 Hz ) of the 1 wt % PEI-BNNSs/EP coating system was 3–4 orders of magnitude higher than the EP coating after 90 days of immersion. The electrochemical results revealed that PEI-BNNSs can significantly enhanced the corrosion resistance of waterborne epoxy coatings.

✓ 已验证 DOI 高影响因子
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DALTON TRANSACTIONS · 2020 ·Vol. 50 ·期 3 ·1060-1068 · IF 4.174

Regioselective B(3)–H bond activation based on an o-carboranyl dithiocarboxylate ligand and its derivatives

Run-Ze Yuan,Peng-Fei Cui,Shu-Ting Guo,Guo-Xin Jin

Herein, we describe the synthesis of tetraphenylphosphonium o-carboranyl dithiocarboxylate (Ligand 1) and methyldithiocarboxyl-o-carborane (Ligand 2). The complexes [Cp*M(o-C2B10H11CS2)Cl] (M = Ir (3); Rh (4)) and [Cp*M(o-C2B10H11CS2)2] (M = Ir (5); Rh (6)) have been synthesized based on Ligand 1. The selective B–H bond activation of Ligand 2 has also been explored, leading to the synthesis of the B–H activated complex [Cp*Ir(o-C2B10H10CS2CH3)Cl] (7) and four of its substituted derivatives (8, 9, 10 and 11). All of these compounds have been characterised through single-crystal X-ray diffraction, NMR, IR spectroscopy and elemental analysis.

✓ 已验证 DOI 高影响因子
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JOURNAL OF THE EUROPEAN CERAMIC SOCIETY · 2019 · IF 4.029

Anisotropic properties of textured h-BN matrix ceramics prepared using 3Y2O3-5Al2O3(-4MgO) as sintering additives

Zhuo Zhang,Xiaoming Duan,Baofu Qiu,Zhihua Yang,Delong Cai,Peigang He,Dechang Jia,Yu Zhou

Textured hexagonal boron nitride (h-BN) matrix composite ceramics were prepared by hot pressing using 3Y 2 O 3 -5Al 2 O 3 (mole ratio of 3:5) and 3Y 2 O 3 -5Al 2 O 3 -4MgO (mole ratio of 3:5:4) as liquid phase sintering additives, respectively. During the sintering process with liquid phase environments, platelike h-BN grains were rotated to be perpendicular to the sintering pressure, forming the preferred orientation with the c -axis parallel to the sintering pressure. Both h-BN matrix ceramic specimens show significant texture microstructures and anisotropic mechanical and thermal properties. The h-BN matrix ceramics prepared with 3Y 2 O 3 -5Al 2 O 3 -4MgO possess higher texture degree and better mechanical properties. While the anisotropy of thermal conductivities of that prepared with 3Y 2 O 3 -5Al 2 O 3 is more significant. The phase compositions and degree of grain orientation are the key factors that affect their anisotropic properties.

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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2022 · IF 7.139

Hydrogen generation over Ni@Pd NCs through an active H-exchange from formic acid-water system

Qu Tang,Xiaobo Zhou,JinXia Liu,Mingmin Wu,Haiwei Ji,Qi Wang,Guo Li,Hui Cong,Yuling Qin

The use of Formic acid as an alternative to fossil fuels is promising, both from economical and ecological standpoints, and has received great of attention owing to its inherently superiority in recent decades. Nevertheless, efficient and low-cost solid catalyst for formic acid dehydrogenation at room temperature still constitutes a biggish challenge. Moreover, comparing to increase the catalytic performance of catalysts, very little attention payed to the kinetic mechanism of dehydrogenation reaction because of the lack of effective characterization artifice. Here, the as-prepared Ni@Pd nanoparticles by a sequential reduction process can be useful catalyst for formic acid decomposition at room temperature without a promoter. Thanks to the effective catalyst and isotope distribution technique, preliminary mechanistic results firstly reveal that hydrogen is obtained via a H-atom recombination on isolated sites after the proton exchange randomly between activated H and solvent.

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JOURNAL OF THE EUROPEAN CERAMIC SOCIETY · 2023 · IF 5.7

Rod-like h-BN modified low carbon Al2O3-C refractory and its high-temperature service performances

Yage Li,Shuaibing Wu,Feng Liang,Gongye Lv,Yu Tian,Haijun Zhang,Yong Liu,Guoqi Liu

Rod-like h-BN with an average diameter of 2 µm was synthesized at a relatively low temperature of 1200 °C through a catalytic pyrolysis precursor strategy using boric acid and melamine as starting materials, and Co(SO 3 NH 2 ) 2 ·4 H 2 O as a catalyst precursor. Subsequently, novel low-carbon Al 2 O 3 -C refractories were prepared via a replacement of the graphite with the as-synthesized rod-like h-BN. When 1 wt% h-BN rods were added to replace graphite, after 3 h coking at 1400 °C, the cold modulus of rupture, cold compressive strength , oxidation resistance , and thermal shock resistance of the specimen were increased by 16.4%, 24.8%, 31.2%, and 52.2%, respectively, compared with these of the control specimen. Moreover, the introduction of h-BN rods in the matrix enhanced the non-wetting ability of the refractory with molten slag, thus the rod-like h-BN modified low carbon refractory presented better slag corrosion resistance with reference to the specimen without h-BN rods.

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Journal of Energy Chemistry · 2023 · IF 13.1

Sn-doped BiOCl nanosheet with synergistic H+/Zn2+ co-insertion for “rocking chair” zinc-ion battery

Yuzhu Qian,Hongrui Wang,Xinni Li,Ting Song,Yong Pei,Li Liu,Bei Long,Xiongwei Wu,Xianyou Wang

The development of insertion-type anodes is the key to designing “rocking chair” zinc-ion batteries. However, there is rare report on high mass loading anode with high performances. Here, {001}-oriented BiOCl nanosheets with Sn doping are proposed as a promising insertion-type anode. The designs of cross-linked CNTs conductive network, {001}-oriented nanosheet , and Sn doping significantly enhance ion/electron transport, proved via experimental tests and theoretical calculations (density of states and diffusion barrier). The H + /Zn 2+ synergistic co-insertion mechanism is proved via ex situ XRD, Raman, XPS, and SEM tests. Accordingly, this optimized electrode delivers a high reversible capacity of 194 mA h g −1 at 0.1 A g −1 with a voltage of ≈0.37 V and an impressive cyclability with 128 mA h g −1 over 2500 cycles at 1 A g −1 . It also shows satisfactory performances at an ultrahigh mass loading of 10 mg cm −2 . Moreover, the Sn-BiOCl//MnO 2 full cell displays a reversible capacity of 85 mA h g −1 at 0.2 A g −1 during cyclic test.

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PROGRESS IN ORGANIC COATINGS · 2017 · IF 2.858

Properties of UV-cured self-healing coatings prepared with PCDL-based polyurethane containing multiple H-bonds

Fei Gao,Jiancheng Cao,Qibo Wang,Ren Liu,Shengwen Zhang,Jingcheng Liu,Xiaoya Liu

A series of ultraviolet (UV)-curable self-healing polyurethane (PU) oligomers were synthesized by incorporating different contents of 2-ureido-4[1H]-pyrimidone and polycarbonate diols (PCDL) with different molecular weights at the end of PU chains. The structure of the oligomers were determined through Nuclear magnetic resonance ( 1 H NMR) and Fourier transform infrared spectroscopy. The PU oligomers were used to produce UV-curable self-healing coatings, the properties of which were investigated and the properties of the coatings with different functionality were studied. The results revealed that the performance of the coating was higher when a higher molecular weight of PCDL was used and With functionality increasing, the crosslinking density of the coating ascends, resulting in higher self-healing temperature and upper pendulum hardness and gloss of the coating. To balance the self-healing ability and mechanical properties of the coating, a series of coating formulations were designed by adding different types and amounts of active diluents. Double bond conversion, thermostability, and self-healing ability were investigated to determine the effect of active diluents on coating performance. The results demonstrated that the resultant coating have excellent adhesion, gloss, and thermostability. Coatings prepared used all types of active diluents had favorable self-healing ability, except for that prepared using 2-acryloyloxymethyl-2-ethyltrimethylene diacrylate. Excellent self-healing and mechanical properties were obtained when 20   w.t.% of triethoxylated trimethylolpropane triacrylate was used.

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ACS Applied Materials & Interfaces · 2017 · IF 7.504

Robust 2D Room-Temperature Dilute Ferrimagnetism Enhancement in Freestanding Ammoniated Atom-Thin [0001] h-BN Nanoplates

Jian-Min Li

The author reports an anthracene vapor-assisted transport growth (∼4.8% in yield) of freestanding atomically thin pristine two-dimensional (2D) hexagonal boron nitride (h-BN) nanoplates directly from bulk powders. A room-temperature dilute magnetism was first observed in the pyrolytic 2D [0001] h-BN nanoplates, which is attributed to the missing N atom numbers (NN) or existence of a nitrogen-vacancy (Nv) with volume fraction ∼1.46%. Upon the postannealing in ammonia, the unsupported ammoniated 2D h-BN nanoplates showed an enhanced robust ferrimagnetism with the effective magnetic moment as high as 0.024 μB/per N, and Néel temperature at 174.9 K. At 295 K, a symmetric electron paramagnetic resonance peak signal was experimentally measured at g ∼ 2.1267, revealing the presence of an unpaired electron trapped at a B atom site in B-rich h-BN. As a promising 2D dilute magnetic semiconductor candidate, our finding favors the ammoniated atom-thin h-BN nanoplate for realization of spintronic nanodevices operating at room temperature.

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