METALLURGICAL AND MATERIALS TRANSACTIONS B-PROCESS METALLURGY AND MATERIALS PROCESSING SCIENCE
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2023
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IF 3
Han Ziqi,Liu Zhihong,Li Qihou,Wang Kai,Yu Zhiqian,Xia Longgong
Ternary compounds in the Al–Te–O system have been considered as potential materials for Low-Temperature Co-fired Ceramics preparation. Two ternary compounds, Al 2 TeO 6 and Al 2 Te 2 O 7 , have been found in the Al–Te–O system under 920 °C in air. The decomposition behavior of these two compounds has been studied with Thermogravimetric Analysis-Differential Scanning Calorimetry (TGA-DSC) and equilibration experiments. Phase equilibrium of the Al 2 O 3 –TeO 2 system has also been experimentally investigated at ambient atmosphere, and corresponding phase diagram has been derived. Obtained results showed that Al 2 Te 2 O 7 , could only be found when TeO 2 was 66.7-70.0 mol pct and temperature was at 590 °C to 610 °C. Al 2 TeO 6 decomposed into Al 2 O 3 , TeO 2 (g), and O 2 (g) when temperature was above 920 °C. Al 2 Te 2 O 7 converted into Al 2 TeO 6 at 620 ± 2 °C, and then followed the decomposition path of Al 2 TeO 6 . In phase equilibrium study, when the initial sample started from the Al 2 O 3 –Al 2 TeO 6 region, Al 2 TeO 6 and Al 2 O 3 were found in quenched samples at the temperature range of 500 °C to 915 °C. When the initial sample started from the Al 2 TeO 6 –TeO 2 phase region, two solid phases, Al 2 TeO 6 and TeO 2 , could be found in samples prepared under 725 ± 2 °C. When the temperature was above 730 ± 2 °C, there were Al 2 TeO 6 and one oxide liquid phase. In the Al 2 Te 2 O 7 –TeO 2 region, all equilibrated samples had Al 2 Te 2 O 7 and TeO 2 .
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JOURNAL OF ALLOYS AND COMPOUNDS
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2023
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IF 6.2
Zhentao Bian,Meng Li,Taoqin Liu,Chengcheng Liu,Yanyan Zhu,Hongxia Cao,Guang Zhu,Hongyan Wang,Chong Chen,Keying Zhang
Recent research interest has increased in the production of heteroatoms-doped porous carbon with controlled morphology from biomass. However, there is still a significant challenge in resolving alkaline solutions that cause equipment corrosion and devising a simple and adaptable approach. In this study, N/O/S co-doped honeycomb-like porous carbons were synthesized from a widely cultivated annual weed ( Hemistepta Iyrata Bunge ) using a simple and eco-friendly method. The sodium hydroxide (NaOH)/urea system was utilized as the pore-forming agent and cellulose solvent, with urea as the nitrogen source. By varying the activation temperature, the as-prepared porous carbon has a high specific surface area (709 m 2 g −1 ), a large total pore volume (0.44 cm 3 g −1 ), and a high heteroatom content of 6.20 at% nitrogen and 8.12 at% oxygen. The prepared porous materials were evaluated as electrodes for supercapacitors . The product (HIB-PHC-750 °C) exhibited a high specific capacitance (353.6 F g −1 at 0.2 A g −1 ) at a carbonization temperature of 750 °C. Additionally, the HIB-PHC-750 °C-based symmetric device with a wide voltage range of 2.0 V possessed a desirable energy density of 44.22 Wh kg −1 at 500 W kg −1 . Moreover, the HIB-PHC-750 °C also demonstrated outstanding cycling stability with 98.2 % capacitance retention after 10,000 cycles. This research provided a facile and favorable alternative method for preparing N/O/S co-doped honeycomb-like porous carbon for electrochemical energy storage devices.
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LWT-FOOD SCIENCE AND TECHNOLOGY
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2023
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IF 6
Jiaxin Chen,Xue Liang,Baohua Kong,Hui Wang,Hongwei Zhang,Jie Tang,Qian Liu,Xin Li
Addition of different (−)-epigallocatechin-3-gallate (EGCG) (0, 100, 200, 500 or 1000 mg/L emulsion) on the interfacial composition and protein-lipid co-oxidation of whey protein isolate (WPI)-stabilised oil-in-water (O/W) emulsions were studied, and underlying mechanisms were also explored. The results indicated that the physical stability of emulsions gradually decreased with the increasing level of EGCG during storage, which clearly verified by decreasing ζ-potential absolute values and increasing droplet size. Moreover, the combination between WPI and EGCG by covalent/non-covalent binding for either adsorbed proteins (AP) or unadsorbed proteins (UAP) led to aggregation and conformational changes in WPI, which confirmed and characterised by electrophoresis, fluorescence quenching, and molecular docking simulation. Meanwhile, the concentration of AP slightly decreased as a function of EGCG level and storage time, however, the UAP showed the opposite change tendency, indicating that EGCG could effectively modulate the interfacial adsorption property of WPI in O/W emulsions. In addition, the incorporation of EGCG efficiently suppressed protein-lipid co-oxidation of O/W emulsions during storage, which was illustrated by hierarchical cluster and correlation analysis between protein and lipid oxidation products. Our results clearly revealed the viability of the EGCG to modulate the interfacial composition and retard the co-oxidation of O/W emulsions with enhanced storability.
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
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2023
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IF 7.2
He Xiao,Xuemin Yang,Man Zhao,Rong Zhang,Yanying Jing,Li Zhang,Yingluo He,Haishun Wu,Jianfeng Jia
To promote kinetic rate of half reactions in water splitting, we synthesized a bifunctional PtFe/graphene with dual active sites by a facile self-designed four-electrode electrochemical method . Characterization data indicate interfacial oxygen bridge structure of Pt–O–Fe is expectedly formed and electrons transfer from Fe to Pt via this bridge structure. This unique interfacial structure not only regulates electronic structure of Pt and Fe, but also offers interfacial electron-transfer channel to improve overall conductivity, which essentially enhances intrinsic activity towards acidic HER and alkaline OER . For HER , the best Pt–Fe/G shows the mass activity of 4239.3 mA mg −1 at −0.063 V, 3.79 times higher than that of Pt/G (1118.5 mA mg −1 ) and 5.02 times higher than that of commercial Pt/C (843.1 mA mg −1 ) catalyst, respectively. Introduction of Fe to Pt decreases the energy barrier of HER process (ΔG∗), and results in conversion of rate-limiting step from H + adsorption (Volmer step) to H∗ desorption (Tafel step). For OER , the greatest PtFe/G exhibits an overpotential of lower 26 mV (10 mA cm-2) than commercial RuO 2 and its mass activity is 16.7 times higher than Fe/G. The formed Pt–O–Fe bond effectively elevates the electrophilic properties and facilitates adsorption of OH − , contributing to the change of rate-limiting step and enormous decrease of reaction activation energy (E a ). This work inspires researchers to construct efficient interfacial oxygen bridge structure to enhance electrocatalytic performance for water splitting and design novel electrochemical method for synthesis of graphene-based composites.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2023
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IF 9.9
Enhui He,Liying Xue,Zheng Wang,Xuefeng Yan,Liangmin Yu
Nowadays, multifunction is regarded as an advanced development direction of new-generation electromagnetic wave absorption (EMWA) materials to fulfill the ever-growing demands in complex environment and situation. Environmental pollution and electromagnetic pollution are all difficult problems for human beings all the time. Now, there is no multifunctional materials for collaborative treatment of environmental and electromagnetic pollution. Herein, We synthesized nanospheres with divinyl benzene (DVB) and N-[3-(dimethylamino)propyl]methacrylamide (DMAPMA), using a simple one-pot method. After calcination at 800 ℃ in N 2 , porous N, O-doped porous carbon materials were prepared. By regulating the mole ratio of DVB and DMAPMA, the ratio was 5:1 reached excellent EMWA property. Remarkably, the introduction of iron acetylacetonate into the reaction of DVB and DMAPMA was effective in enhancing the absorption bandwidth to 8.00 GHz at a 3.74 mm thickness, which depended on the synergistic effects from dielectric and magnetic losses. Simultaneously, the Fe-doped carbon materials had a methyl orange adsorption capacity. The adsorption isotherm conformed to the Freundlich model. After methyl orange absorption, the EMWA property did not greatly change. Thus, this research paves the way for the creation of multifunctional materials to solve environmental pollution and electromagnetic pollution together.
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PubMed
高影响因子
FOOD RESEARCH INTERNATIONAL
·
2023
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IF 8.1
Jiaxin Chen,Junjie He,Zihan Zhao,Xin Li,Jie Tang,Qian Liu,Hui Wang
This work aimed to investigate the effects of heat treatments at different temperatures (60, 70 and 90 °C, expressed as HT-60, HT-70 and HT-90) on interfacial composition and protein-lipid co-oxidation in whey protein isolate (WPI)-stabilised O/W emulsions during storage. Compared with control group, all heated emulsions exhibited weaker physical stability over 10 days of storage, which verified by the increased droplet size, as well as decreased adsorbed protein levels and absolute ζ-potential values. Moreover, proteins recovered from the HT-90 emulsion showed the highest fluorescence intensity and red-shift of the maximum emission wavelength, indicating partial unfolding of the protein structure. Meanwhile, severe changes in protein structure were also observed in the HT-70 and HT-90 emulsions, which clearly verified by the degradation of bovine serum albumin, α-lactalbumin and β-lactoglobulin. Furthermore, HT-70 and HT-90 emulsions showed lower levels of lipid hydroperoxides and thiobarbituric acid reactive substances. In contrast, the recovered proteins were subject to severe oxidative stress as indicated by carbonyl and N’-formyl-L-kynurenine. Hierarchical cluster and correlation analysis implied that the process of protein-lipid co-oxidation is inevitable, but it can be retarded by heat treatment. Our results clearly revealed the relevance among heat treatment, interfacial adsorption property, and the protein-lipid co-oxidation of O/W emulsions.
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PubMed
高影响因子
AICHE JOURNAL
·
2023
·Vol. 69
·期 9
·e18149
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IF 3.7
Yongxiao Tuo,Ying Meng,Qing Lu,Qing Wang,Furong Jia,Yan Zhou,Xiang Feng,Jun Zhang,Xuezhi Duan,De Chen
The enhancement of catalytic activity is always limited by the dilemma in activation and desorption due to Sabatier principle. Locating the Sabatier optimum by manipulating catalyst electronic structure has been a long-standing challenge in heterogeneous catalysis. Herein, we presented a generic strategy to continuously tailor the Pt 5d state occupancy via tuning the Pt O Mn electronic linkage over Al 2 O 3 -confined MnO x islands, aiming at accommodating the C H cleavage and product desorption capabilities in dehydrogenation of liquid organic hydrogen carriers (monocyclic/bicyclic hydrides). Rising Mn valence can decrease the Pt 5d state occupancy through more electron transfer from Pt 5d to O 2p due to the strong π-donation of O 2p to Mn 3d. This will lead to the lower initial C H activation energy barrier while higher product desorption energy barrier. An intermediate Pt 5d filling of ~8.4 in Pt Mn 2 O 3 /Al 2 O 3 enables the balanced level of product desorption and C H activation, thus ensuring a superior dehydrogenation activity. The electron structure-adsorption-performance modulation mechanism described herein provides a benchmark to locate the Sabatier optimum for the metal catalyst design.
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY
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2023
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IF 4.5
Jifang Zhang,Chengcheng Suo,Jinde Sun,Wei Li,Sha Luo,Chunhui Ma,Shouxin Liu
In this study, C α –C β and C β –O bond cleavage of β-O-4 model compound (2-phenoxy-1-phenylethanol) were accomplished by electrocatalysis depolymerization process in deep eutectic solvents (DES) systems. We have investigated the application of Ni-Co/C catalysts on working electrode, which were synthesized with impregnation method. The Ni-Co/C with porous structure and abundant active sites, was shown an excellent electrocatalysis activity. Specific structure of Ni-Co/C could provide greatly efficient adsorption and desorption capacity to promote C α –C β and C β –O bond cleavage. Therefore, in this electrocatalysis depolymerization process, the highest depolymerization rate exceeded 90%. And the yields (and conversion rates) of products (including benzaldehyde, acetophenone, benzoic acid, phenol) can reach to 124.08 mg/g (25.05%), 23.29 mg/g (4.15%), 44.64 mg/g (7.83%), 30.3 mg/g (6.9%). Furthermore, the electrocatalysis mechanism of C α –C β and C β –O bond was investigated. The cleavage of C α –C β and C β –O bond was initiated by in situ generated free radicals through Ni-Co/C. Then, the cleavage of C α –C β and C β –O bond were occurred by ·OH and ·O 2 − . The results were showed that the C α –C β bond cleavage was more in line with the β-C elimination and free radical pathways, and C β –O bond cleavage was consistent with direct oxidative addition. The enhanced electrocatalytic efficiency of the low-cost Ni-Co/C electrocatalyst combined with its good chemical stability and selectivity, which offer a promising route for developing an efficient lignin depolymerization technology.
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Catalysis Science & Technology
·
2019
·Vol. 9
·期 10
·2651-2663
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IF 5.726
Hairus Abdullah,Dong-Hau Kuo,Noto Susanto Gultom
Hydrogen-evolved Dy-doped Zn(O,S) photocatalysts with different amounts of Dy precursor have been synthesized, characterized and further utilized for hydrogenation reactions. The Dy catalysts are first examined using electrochemical impedance spectroscopy, photo responsivity, and the hydrogen evolution reaction. Dy-doped Zn(O,S) with 10% Dy precursor shows the best photocatalyst performance with the highest H2 production rate of 8.160 mmol g−1 h−1. This catalyst is chosen for conducting the hydrogenation reaction. It is our intention to confirm the correlation between the photocatalytic H2 production rate and the hydrogenation reactions of 4-nitrophenol to 4-aminophenol and azobenzene to aniline, which is a step further in the hydrogenation reaction to challenge the NN bond cleavage of azobenzene. A 100% photo conversion of 60 ppm azobenzene to aniline in 6 h was confirmed under a low-power UV light illumination in a 10% ethanol solution. Kinetic steps and kinetic mechanisms are proposed, which involve the important reaction steps of solvation, adsorption, pinning, and surface hydrogenation reaction operating together.
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JOURNAL OF COORDINATION CHEMISTRY
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2018
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IF 1.703
Guo-Cheng Liu,Yan Li,Ying Xiong,Xiang-Xiang Liu,Qiao-Min Li,Ju-Wen Zhang,Hong-Yan Lin,Xiao-Wu Li
To investigate the effect of the spacers of S-/O-bridged dipyridylamides on the structures of Co(II)/Zn(II) complexes, [Co(L1)(chda)]·1.5H2O (CP1), [Co(L2)(chda)] (CP2), [Zn(L1)(hip)]·DMA·2H2O (CP3), and [Zn(L2)(hip)]·2.8H2O (CP4) [L1 = N,N′-bis(pyridine-3-yl)thiophene-2,5-dicarboxamide, H2chda = trans-1,4-cyclohexanedicarboxylic acid, L2 = N,N′-bis(pyridine-3-yl)-4,4′-oxybis(benzoic) dicarboxamide, H2hip = 5-hydroxyisophthalic acid, DMA = N,N-dimethylacetamide], have been solvothermally synthesized. X-ray single-crystal diffraction shows that CP1 is a 2-D 3,5-connected network based on Co-L1 linear chains and (Co-chda)2 double chains. CP2 features a 1-D structure derived from 1-D wave-like (Co-chda)2 double chains decorated by terminal L2 ligands. CP3 and CP4 show wave-like (4,4) networks constructed by 1-D Zn-L1 zigzag and Zn-hip zigzag (for CP3)/linear (for CP4) chains. The effect of the spacers of S-/O-bridged dipyridylamides on the structures of the title complexes was discussed. Electrochemical behaviors of CP1–CP2 and solid-state luminescent properties of CP3–CP4 were studied. The luminescence investigations show that CP3 and CP4 are recycled fluorescent probes for environmentally relevant Fe3+ ions. The photocatalytic properties for the degradation of methylene blue (MB) under ultraviolet light irradiation of CP3–CP4 and the recyclable materials after fluorescent sensing Fe3+ ions (named CP3@Fe3+ and CP4@Fe3+) have also been investigated.
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Catalysts
·
2018
·Vol. 8
·期 8
·296
·
IF 3.465
Shuqi Fang,Kang Bi,Qiao Zhang,Lingpeng Chen,Yongming Sun,Hongyu Huang,Longlong Ma,Chenguang Wang
Layered double hydroxide (LDH) is a layered solid containing positively charged layers with negatively charged anions as an interchangeable interlayer. In this research, Mg(Al)O supports were synthesized with three different Mg:Al molar ratios, and bimetallic PtSn catalysts were loaded onto the supports via the anion exchange method. The properties of ethane dehydrogenation of the PtSn/Mg(Al)O catalysts were investigated. The results show that the structure and properties of the PtSn/Mg(Al)O catalysts were influenced by the Mg:Al molar ratio of the hydrotalcites, which consequently influenced the ethane dehydrogenation performance. When the Mg:Al ratio was 5:1, the ethane dehydrogenation performance was optimal, relative to the Mg:Al ratios of 2:1 and 10:1.Keywords:hydrotalcite;Mg:Al molar ratio;anion exchange method;ethane dehydrogenation
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CERAMICS INTERNATIONAL
·
2024
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IF 5.1
Jianjian Wang,Yue Yu,Zhiqiang Li,Hualin Wang,Shimin Liu,Tingting Yao,Weiwei Jiang,Nan Wang,Chaoqian Liu,Wanyu Ding,Zhihua Zhang,Chuang Dong
Multi-component high entropy oxides (HEOs) have attracted enormous attention due to their unique structures and potential applications. The conventional selection strategy to obtain HEOs is to search for equimolar cationic systems to maximize configurational entropy and avoid phase separation. We previously explored non-equimolar cationic rocksalt structure Mg–Co–Ni–Cu–Zn–O HEOs using cluster-plus-glue-atom model. In this paper, the mixing entropy, enthalpy and Gibbs free energy of constructed superclusters were numerically calculated and compared with the correlated crystal structure based on recent studies. It indicated the Gibbs free energy rather than mixing entropy agrees well with the phase stability of HEOs. Mg 28 Co 17 Ni 19 Cu 16 Zn 16 O 96 shows the optimal phase stability which is related to the lowest Gibbs free energy, reflecting a regular octahedral environment preferred by the cation composition in the system. Enthalpy and entropy are among important design criteria in determining the phase stability of HEOs but the function of enthalpy is obviously higher than that of entropy. This study provides a comprehensive way to access HEOs which is undoubtedly very important for the development of other non-equimolar cationic high entropy materials such as carbides , silicides , borides or nitrides .
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危险品化学品经营许可证（带存储）