APPLIED CATALYSIS B-ENVIRONMENTAL
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2019
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IF 14.229
Ling Zhang,Yiquan Xie,Yiwen Jiang,Yaobin Li,Chunying Wang,Shichao Han,Huimin Luan,Xiangju Meng,Feng-Shou Xiao
Catalytic combustion at low temperature has been considered as an effective route for removal of indoor HCHO pollutant, and conventional catalysts are supported noble metal nanoparticles, which are costly for wide applications. Solution of this issue is to use relatively low metal catalysts. Herein, we report that Mn-promoted Ag catalyst supported on pure silica Beta zeolite with a good hydrophobicity is very active for catalytic combustion of HCHO. By optimizing the loadings of Ag and Mn, it is found that 10 wt% Ag with 8 wt% Mn (10 %Ag8 %Mn/Beta-Si) exhibits highest activity, giving the complete HCHO conversion at around 45 °C, which steadily outperform the temperatures (70–145 °C) for full oxidation of HCHO reported previously. The choice of Ag loading with 10 wt.% is due to the highest exposed surface of Ag sites, and the use of Mn loading with 8 wt% is assigned to the balance of density and mobility for active oxygen species in the catalysts. The strategy combining the hydrophobic supports with optimized active oxygen species might offer an alternative way to develop highly efficient heterogeneous catalysts for the removal of air pollutants in the future.
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高影响因子
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
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2019
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IF 3.375
Siqian Zhang,Cheng Zhang,Qiang Wang,Wha-Seung Ahn
A series of ZSM-5 catalysts were synthesized using fly ash from power plants and red mud from aluminum production in different weight ratios. The ZSM-5 was subsequently coimpregnated with Co and Mn and tested for the low-temperature selective catalytic reduction of NOx by NH3 (NH3-SCR). These catalysts were characterized by XRD, N2-adsorption isotherms, SEM, XPS, and H2-TPR. Among all the prepared catalysts, 5 wt % Co 10 wt % Mn/ZSM-5 had shown the best catalytic activity, with 98.8% conversion of NOx and 90.7% selectivity toward N2 at 150 °C. This is comparable to the performance of a similar ZSM-5 catalyst prepared using chemical reagents. The high ratio of Mn4+/(Mn4+ + Mn3+ + Mn2+) in the catalyst improved the NOx conversion, whereas the moderate redox property imparted by Co3+ led to high N2 selectivity. This catalyst also showed strong resistance against poisoning in 100 ppm SO2 and 5% H2O. This work demonstrates that effective NOx removal treatment with high N2 selectivity and sufficient stability for either cement plants or incinerators can be achieved by using a porous catalyst/support material produced from industrial solid wastes.
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高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2019
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IF 3.131
Boqiong Jiang,Beilong Lin,Zhiguo Li,Shuang Zhao,Ziying Chen
A series of Mn/TiO 2 catalysts were prepared by ultrasonic spray pyrolysis (USP) method for selective catalytic reduction (SCR) of NOx from flue gas at low temperatures. The highest activity of Mn/TiO 2 was obtained with a Mn/Ti ratio of 0.5. When Fe was doped into Mn(0.5)/TiO 2 , the NOx conversion rate on Fe(0.05)-Mn(0.5)/TiO 2 was increased by approximately 10 % at 120–180 °C. The samples were characterized by XRD , SEM , H 2 -TPR, and N 2 adsorption analyses. Results revealed that Mn(0.5)/TiO 2 with Mn/Ti ratio of 0.5 presented the lowest crystallinity , the highest surface area, and the highest redox ability. Although the surface area was significantly decreased by Fe doping, it also reduced the crystallinity and crystal size of the catalysts, thereby increasing the O concentration on the surface of catalyst. Moreover, Fe(0.05)-Mn(0.5)/TiO 2 displayed a higher redox ability than the other catalysts. At 120–240 °C, the activation energy decreased from 27.65 kJ/mol on Mn(0.5)/TiO 2 to 14.46 kJ/mol on Fe(0.05)-Mn(0.5)/TiO 2 , thereby facilitating the activation of the reaction on Fe(0.05)-Mn(0.5)/TiO 2 . Despite that the NO and NH 3 adsorptions were lower on Fe(0.05)-Mn(0.5)/TiO 2 than on Mn(0.5)/TiO 2 , the intermediates on Fe(0.05)-Mn(0.5)/TiO 2 , particularly nitrates, were easily activated to participate in the reaction, leading to increasing catalytic activity.
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CHEMICAL ENGINEERING JOURNAL
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2022
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IF 16.744
Yuanzhi Luo,Pan Wang,Gaixia Zhang,Sisi Wu,Zhangsen Chen,Hariprasad Ranganathan,Shuhui Sun,Zhicong Shi
To realize highly efficient and stable hydrogen production at high current densities, more efforts are devoted to developing outstanding water-splitting electrocatalysts. Herein, through a facile hydrothermal-phosphorization method, Mn-doped Ni 2 P/Fe 2 P was rationally designed and prepared as a high-performance bifunctional electrocatalyst for alkaline freshwater/seawater splitting. In alkaline seawater (freshwater) electrolyte, it merely needs low overpotentials of 358 (3 3 5) and 470 (4 0 5) mV to reach 1000 mA cm −2 for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER), respectively. This electrocatalyst also shows excellent stability even at a high OER current density of 500 mA cm −2 for 200 h. Regarding the alkaline overall seawater splitting, Mn-doped Ni 2 P/Fe 2 P presents a low cell voltage of 2.02 V at 500 mA cm −2 and outstanding stability for 120 h at the same current. The X-ray absorption fine structure (XAFS) experimental analysis verifies that the Mn doping and Ni 2 P/Fe 2 P heterointerfaces can efficiently optimize the electrocatalyst’s electronic structure, leading to the improved intrinsic OER and HER activities. Meanwhile, the 3D nanoflower structure provides abundant exposed active sites, and the Mn doping and heterointerfaces can create more active sites. Besides, the high corrosion resistance resulting from nickel-iron phosphides makes the electrocatalyst become a good candidate for seawater splitting. This study provides a simple path to fabricate highly active and robust non-noble electrocatalysts for freshwater/seawater splitting at high current densities.
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ANALYTICAL SCIENCES
·
2022
·Vol. 39
·期 1
·13-22
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IF 1.967
Chen Xianli,Liu Yi,Zhong Ming,Yang Jiangyong,Lin Zhenming,Liang Yong
Sialic acid (SA), known as N -acetyl neuraminic acid, is a natural 9-carbomonosaccharide derivative. SA has been widely applied in the early diagnosis of diseases as therapeutic target. However, the abundance of SA is very low in biological samples, which is usually interfered by the similar molecules coexisting at high abundance. Combining the advantages of high selectivity and specificity of molecularly imprinted technology, high specific surface area of mesoporous materials and excellent optical properties of quantum dots, we chose Mn-doped ZnS quantum dots as signal elements, and sialic acid as the template molecule. KH-4-MAPB with recognition ability to SA was synthesized by one-step hydrothermal method using thiolene click reaction as functional monomer. Based on the principle of boron affinity, molecularly imprinted polymers with highly ordered mesoporous structure were prepared, and the structure and fluorescence properties of fluorescent molecularly imprinted polymers were studied. FT-IR, XRD, TEM and nitrogen adsorption–desorption experiments were used to characterize the structure and morphology of the molecularly imprinted polymers. The results showed that the prepared molecularly imprinted polymers had highly ordered mesoporous structure and a large number of imprinted holes, which ensured the specific selectivity of the molecularly imprinted polymers. The fluorescence properties of MIMPs were characterized and analyzed by fluorescence spectra, equilibrium adsorption kinetics experiments were conducted and imprinting properties were recorded under different pH. The above experimental results showed that the fluorescence quenching was successfully achieved when the template molecule SA was captured by the molecularly imprinted polymer. When the concentration of SA was 1.25–100 × 10 –2 g/L, the fluorescence quenching degree of MIMPs showed a fine linear relationship with SA. The correlation coefficient was 0.9946, and the detection equation was F 0 / F − 1 = 0.0215 [CSA] + 0.0241. MIMPs had a high recognition ability for SA, and the imprinting factor was 2.44. As a fluorescent sensor for SA, the response time of MIMPs was 20 min. When the buffer solution pH was 7, the imprinting factor was the largest. Under the best conditions, MIMPs revealed good selectivity and specificity for the fluorescence recognition of SA. MIMPS were also applied to the analysis of SA in real human serum samples with satisfactory results. Graphical abstract
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PubMed
高影响因子
RARE METALS
·
2023
·Vol. 43
·期 1
·148-163
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IF 8.8
Xu Zhi-Hui,Sun Shi-Shuai,Li Xue-Lei,Zhang Zhi-Hui,Li Hai-Ying,Ruan Shuang-Ting,Yin Shou-Gen
The balancing of the electrochemical performance, mechanical stability, and processing technology for applying supercapacitors to flexible and wearable electronics continues to encounter severe challenges. Herein, we prepare Ni–Co–Mn hydroxide electrodes with a three-dimensional multichannel structure via a simple hydrothermal method. These are constructed using vertically contiguous nanosheets with a uniform thickness and rough surface. The electrodes can provide numerous electroactive sites and accelerate the transmission of electrolyte ions. The relationship between the structure and electrochemical performances is verified by experiments and theoretical calculations. Two-dimensional (2D) planar and one-dimensional (1D) fiber electrodes are prepared using a flexible carbon cloth (CC) and carbon fiber (CF), respectively, as substrates. The assembled quasi-solid-state flexible asymmetric supercapacitor (FASC) with a two-dimensional sandwich structure using NiCoMn–OH/CC as the electrode achieves a remarkable energy density of 73.8 Wh·kg −1 at a power density of 1.03 kW·kg −1 . The quasi-solid–state FASC with a 1D linear structure using NiCoMn–OH/CF as the electrode also attains a high energy density (12.9 Wh·kg −1 at a power density of 0.75 W·kg −1 ). Moreover, the electrochemical performances of the NiCoMn/CC//AC/CC and NiCoMn/CF//AC/CF FASCs are not disturbed at different bending angles (0°, 45°, 90°, 135° and 180°). This indicates the superior flexibility of the devices. We also assemble a self-powered energy-harvesting storage system by integrating FASCs and commercial solar cells to verify its practicability. It displays sustainable development potential for energy storage. Graphical abstract
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CHEMICAL ENGINEERING JOURNAL
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2023
·
IF 15.1
Zhuolin Cui,Tingting Hu,Shuqing Yang,Yu Yang,Xueyan Liu,Tao Wang,Huizhi Chen,Chunlai Zeng,Ruizheng Liang,Yubin Zhou
Sonodynamic therapy (SDT) has attracted increasing attention owing to its superior tissue penetration compared with other therapies. However, the development of multifunctional sonosensitizers with imaging capability and high production efficiency of reactive oxygen species (ROS) is still a challenge for current sonodynamic cancer therapy. Herein, we report the design and preparation of amorphous 2D Mn-doped CoMo-layered double hydroxide (a-Mn-CoMo-LDH) nanosheets (NSs) through acid etching-induced crystalline-to-amorphous phase transformation as a highly active nano-agent for magnetic resonance imaging (MRI)-guided SDT. The a-Mn-CoMo-LDH NSs exhibit superior ROS production capacity compared with amorphous CoMo-LDH NSs (∼1.3 times) and crystalline Mn-CoMo-LDH NSs (∼3.9 times) under ultrasound (US) irradiation, which is ∼ 9.9 times of the previously reported TiO 2 sonosensitizer. The doped Mn 4+ in the a-Mn-CoMo-LDH NSs can not only decompose H 2 O 2 into O 2 to alleviate the hypoxia level in tumor microenvironment (TME), but also consume glutathione (GSH) to reduce its clearance of ROS, promoting the SDT performance synergistically. Importantly, the GSH consumption can partially reduce the Mn 4+ to Mn 2+ within the tumors, which can serve as an agent for T 1 -weighted MRI, thus endowing the a-Mn-CoMo-LDH NSs with excellent MRI capability. Therefore, the as-prepared a-Mn-CoMo-LDH NSs with polyethylene glycol modification can be used as an efficient nano-agent for MRI-guided SDT, which can effectively achieve apoptosis of cancer cells in vitro and eradication of tumors in vivo under US irradiation.
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高影响因子
ACS Applied Energy Materials
·
2023
·
IF 6.4
Yuqing Hu,Puhui Deng,Wenying Wang,Linping Zhang,Yu Hou
Element doping and collaboration with other cocatalysts are two vital strategies to improve the photoelectrochemical properties and overcome the drawbacks of CdS for better photocatalytic performance. In this work, a series of manganese cadmium sulfides (MnxCd1–xS) were obtained by a solvothermal method. When x is equal to or greater than 0.3, MnxCd1–xS is composed of Mn–Cd–S sosoloid and MnS. Among all these MnxCd1–xS products, the Mn0.5Cd0.5S sample showed the best photocatalytic hydrogen production (5.99 mmol g–1 h–1). To further elevate the hydrogen production rate of Mn0.5Cd0.5S, four kinds of Ni-POMs were coupled with it as cocatalysts, and all these composite photocatalysts displayed enhanced performance. The highest efficiency was observed for 15-Ni4–Mn0.5Cd0.5S, which is up to 36.58 mmol g–1 h–1. Various characterizations indicated that Ni4P2W18, Mn–Cd–S sosoloid and MnS in the 15-Ni4–Mn0.5Cd0.5S composite form a double type-II heterojunction, which facilitates the separation and transfer of photogenerated carriers.
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高影响因子
Crystals
·
2023
·Vol. 13
·期 11
·1587
·
IF 2.7
Yiyi Xiao,Hui Huang,Jinkun Guo,Mi Yan,Liyuan Wei,Yu Liu,Shiliang Huang,Rufang Peng,Bo Jin
Energetic complexes represent a crucial research direction for the design and synthesis of novel energetic materials. In this work, 2,6-diamino-3,5-dinitropyrazine-1-oxide (LLM-105), a significant explosive compound with exceptional comprehensive properties, was selected as the ligand for coordinating with various metal ions. Four novel energetic complexes, Ni(C4H3N6O5)2·DMF (1), Co(C4H3N6O5)2·2DMF (2), Mn(C4H3N6O5)3·3/2DMF (3), and Cu3(C4H2N6O5)3·3DMF (4) were successfully synthesized, and their crystal structures were identified by a single-crystal X-ray diffraction technique. The structural analyses illustrated that LLM-105 can form either a mononuclear metal complex after the deprotonation of one amino group or a trinuclear metal complex after the deprotonation of two amino groups. Compound1exhibits a planar quadrilateral geometry, while both compounds2and3display distorted octahedral configurations. Compound4has three metal centers and exhibits two coordination configurations of distorted tetragonal pyramid geometry and planar quadrilateral geometry. The detonation performances of compounds1–4were also theoretically calculated, revealing their favorable explosive properties. These findings emphasize the diverse coordination modes of LLM-105 and the structural variability and adjustability of its complexes, offering valuable insights for regulating both the structure and performance of the LLM-105 complex as well as researching its deprotonation.Keywords:energetic complexes;LLM-105 ligand;single-crystal structure;coordination modes
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高影响因子
INORGANICA CHIMICA ACTA
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2023
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IF 2.8
Qiang Zhao,Qi-Yang Li,Zhi Shen,Guo Zang,Wen-Jun Lv
In order to further enrich the research on the synthesis of complexes with terpyridine ligand and transition metals, in this work, 4′-(4-(1H-imidazol-1-yl)phenyl)-2,2′:6′,2′'-terpyridine (Iptpd), 1,2-benzenedicarboxylic acid (1,2-BA) were used to construct metal complexes with Cd 2+ , Zn 2+ , Mn 2+ and Co 2+ by solvothermal reaction, and five complexes were constructed, namely, [Cd(Iptpd)(NO 3 ) 2 ] n ( 1 ), [Mn(Iptpd)(NO 3 ) 2 ] n ( 2 ), [Zn(Iptpd) (NO 3 ) 2 ·2H 2 O] n ( 3 ), [Mn(Iptpd)(1,2-BA)] 2 ( 4 ) and [Co 3 (Iptpd) 2 (1,2-BA) 2 (NO 3 ) 2 ·10H 2 O] n ( 5 ); Single crystal x-ray diffraction analyses reveal that complexes 1, 2, 3 and 5 have one-dimensional chain structure, 4 is a binuclear structure. In addition, Luminescence behavior of complexes 1 and 3 , magnetic properties of complexes 2 and 4 were investigated. The fluorescent test result shows that complex 1 and 3 have weak fluorescence performance and the fluorescence intensity is lower than that of ligand; The magnetic results indicate that complex 2 has ferromagentic property and 4 has antiferromagentic property.
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NEW JOURNAL OF CHEMISTRY
·
2023
·Vol. 47
·期 43
·19974-19982
·
IF 3.3
Hao Fan,Qin Peng,Zhenxing Shen,Xuefeng He,Yiming Yang
Nitric oxide (NO), a major atmospheric pollutant and a precursor to haze, can be removed using the denitration catalyst. Mn and Ni are commonly used as denitration catalyst additives owing to their adsorption abilities for NO and ammonia (NH3). In this study, we synthesized Mn- and Ni-loaded Pt-modified sulfated cerium oxide (PtSCe) catalysts using an impregnation method and explored the effects of these elements. The results revealed that the two elements had contrasting effects on the denitration activity of the catalysts. Mn improved the water vapor and sulfur resistance of the PtSCe sample by increasing the concentration of weak acid sites, enhancing the redox ability, and increasing the content of surface-adsorbed oxygen. The elevation in oxygen vacancies, stimulated by the presence of Ce3+ and Mn3+, swiftly replenished the reactive oxygen species, thereby sustaining the high denitration efficiency of the MnPt/SCe sample. Active sites on the catalyst surface included NH3 adsorbed on Lewis acid sites, NH4+, and –NH2, along with bridging, monodentate, and bidentate nitrate groups. Regarding the catalyst reaction mechanism, we determined that the selective catalyst reduction of NH3-SCR over MnPt/SCe followed both the Eley–Rideal and Langmuir–Hinshelwood mechanisms. These findings offer crucial insights into the intricate relationship between metals, sulfates, and carrier molecules, thus providing implications for future catalyst design.
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MOLECULES
·
2023
·Vol. 28
·期 19
·6843
·
IF 4.6
Fumei Shi,Yilan Chen,Chuanheng Dong,Jiajia Wang,Chunman Song,Yalin Zhang,Zhen Li,Xianqiang Huang
Polyoxometalates (POMs) exhibit unique structural characteristics and excellent physical and chemical properties, which have attracted significant attention from scholars in the fields of anticancer research and chemotherapy. Herein, we successfully synthesized and structurally characterized two novel polyoxovanadates (POVs), denoted as POVs-1and POVs-2, where [M(1-vIM)4]2[VV4O12]·H2O (M: NiIIand MnII, 1-vinylimidazole abbreviated as 1-vIM) serve as ligands. The two POVs are isomeric and consist of fundamental structural units, each comprising one [V4O12]4−cluster, two [M(1-vIM)4]2+cations, and one water molecule. Subsequently, we evaluated the cell viability of human hepatocellular carcinoma (HepG-2) cells treated with the synthesized POVs using the MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazoliumbromide) assay. And the changes in cell nucleus morphology, mitochondrial membrane potential (Δψm), and reactive oxygen species levels in HepG-2 exposed to POVs were monitored using specific fluorescent staining techniques. Both hybrid POVs showed potent inhibitory activities, induing apoptosis in HepG-2 cells along with significant mitochondria dysfunction and a burst of reactive oxygen species. Notably, the inhibitory effects of POVs-2were more pronounced than those of POVs-1, which is primarily attributed to the different transition metal ions present. These findings underscore the intricate relationship between the metal components, structural characteristics, and the observed antitumor activities in HepG-2 cells.Keywords:polyoxovanadates;imidazole ligands;human hepatocellular carcinomas;anticancer;apoptosis
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高影响因子
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