CATALYSIS LETTERS
·
2023
·
IF 2.8
Chen Yiming,Hou Zhanggui,Wang Chuan,Ma Xin,Yang Hong,Wang Wen,Zhou Ling,Zhang Yi
As well known, the industrial methanation process needs highly active and stable catalysts obtained from cheap and abundant elements. In this work, we propose a high-loaded Ni/Al 2 O 3 catalyst promoted by manganese. Among them, the 20Ni2Mn/Al 2 O 3 catalyst exhibits the best CO 2 conversion (90.5%) and excellent methanation stability at 250 °C. In addition, the roles of the Mn promoter on CO 2 conversion and selectivity were investigated in detail. The features of natural and promoted catalysts are described through XRD, XRF, BET, TEM, H 2 -TPR, CO 2 -TPD, and operando DRIFTS techniques. Based on various characterization results, the addition of Mn will greatly reduce the Ni particle size and improve the Ni dispersion on the alumina support. Furthermore, compared to the unpromoted catalyst, Mn promoted catalysts show better reducibility and have more medium basic sites. And these medium basic sites are favorable to the adsorption and activation of CO 2 . In-situ DRIFTS experiments for CO 2 methanation reveal that manganese could promote the monodentate carbonate hydrogenated to formate rapidly, which could be faster converted towards CH 4 , contributing to significantly improved activity of the Mn promoted Ni/Al 2 O 3 catalyst. Graphical Abstract
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MOLECULES
·
2023
·Vol. 28
·期 11
·4411
·
IF 4.6
Fuhua Wei,Kui Wang,Wenxiu Li,Qinhui Ren,Lan Qin,Mengjie Yu,Zhao Liang,Meng Nie,Siyuan Wang
This work studies the use of Fe/Ni-MOFs for the removal of ciprofloxacin (CIP) in wastewater. Fe/Ni-MOFs are prepared by the solvothermal method and characterized by X-ray diffraction (XRD), a scanning electron microscope (SEM), Fourier transform infrared spectroscopy (FT-IR), and a thermal gravimetric analyzer (TG). Under the conditions of the concentration of 50 ppm, a mass of 30 mg, and a temperature of 30 °C, the maximum adsorption capacity of ciprofloxacin removal within 5 h was 232.1 mg/g. The maximum removal rate was 94.8% when 40 mg of the Fe/Ni-MOFs was added to the solution of 10 ppm ciprofloxacin. According to the pseudo-second-order (PSO) kinetic model, the R2values were all greater than 0.99, which proved that the adsorption theory of ciprofloxacin by Fe/Ni-MOFs was consistent with the practice. The adsorption results were mainly affected by solution pH and static electricity, as well as other factors. The Freundlich isotherm model characterized the adsorption of ciprofloxacin by Fe/Ni-MOFs as multilayer adsorption. The above results indicated that Fe/Ni-MOFs were effective in the practical application of ciprofloxacin removal.Keywords:metal–organic frameworks;antibiotics;adsorption
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高影响因子
CATALYSIS LETTERS
·
2023
·
IF 2.8
Zhu Peng,Han Chunyang,Xia Haian
Catalytic hydrogenolysis of xylose to ethylene glycol (EG) and 1,2-propanediol (1,2-PG) is an important way for the high-value valorization of biomass. Herein, Ni-W/CeO 2 catalysts prepared by incipient-wetness impregnation method were used for the hydrogenolysis of xylose to EG and 1,2-PG. Several characterizations such as X-ray diffraction (XRD), Transmission electron microscopy (TEM) and X-ray photoelectronic spectroscopy (XPS) were used to analyze the physicochemical properties of the catalysts. The effects of different Ni/W ratios and reaction conditions on the hydrogenolysis performance of the catalyst were investigated. The doping of W promoted the selective cleavage of C–C and C-O bonds of xylose, thus improved the yield of EG 1,2-PG. The doping of W can form interactions with Ni and increase the oxygen vacancy concentration of CeO 2 , which have a significant impact on the catalyst activity. When the Ni: W ratio is around 1:1, the catalyst has the best activity, and the total yield of diols can reach about 43.2%.. When xylan was used as the substrate, the total yield of diols can reach to 58.7%. The possible reaction mechanism of xylose hydrogenolysis was also discussed. This work developed a new catalyst system for the directional conversion of xylose to EG and 1,2-PG, which provided a new idea for the design of catalyst to converting lignocellulose, especially carbohydrate into high-value chemicals. Graphical Abstract Ni-W/CeO 2 with different Ni/W ratio are efficient catalysts for hydrogenolysis of xylose to EG and 1,2-PG.
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International Journal of Electrochemical Science
·
2023
·
IF 1.5
Jie Yuan,Hui Zhao,Ruizhuo Ouyang,Yuqing Miao
In this work, nanorod bundles of Ni-Mo-O were synthesized within nickel foam (NF) using a conventional hydrothermal method, which was the further vulcanized to form Ni-Mo-S upon doping sulfur. The NF/Ni-Mo-O and NF/Ni-Mo-S materials were characterized in terms of their morphology, composition and electrochemical properties. NF/Ni-Mo-O showed excellent performance as a supercapacitor. In addition, NF/Ni-Mo-S catalyzed the electrochemical oxidation of glucose in alkaline medium, exhibiting its potential application as a new fuel cell. Their excellent electrochemical performances greatly benefited from the preferred activity of NF/Ni-Mo-O and NF/Ni-Mo-S, efficient electron transfer over the electrode and high conductivity of NF.
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ADVANCED FUNCTIONAL MATERIALS
·
2023
·Vol. 33
·期 44
·2303986
·
IF 19
Xuefei Xu,Habib Ullah,Muhammad Humayun,Linfeng Li,Xia Zhang,Mohamed Bououdina,Damien P. Debecker,Kaifu Huo,Deli Wang,Chundong Wang
Constructing multiple heterogeneous structures allows for improving the electrocatalytic activity of NiO by incorporating multiple active sites. Unfortunately, the poor conductivity of NiO makes efficient charge transfer within the heterogeneous structures difficult, thereby inhibiting the improvement of its intrinsic activity. Herein, F-doped NiO/Ni@C heterogeneous catalyst (F-NiO/Ni@C) is fabricated via a new organic-inorganic hybrid approach, showing both advanced hydrogen evolution reaction (HER) and urea oxidation reaction (UOR) activity. The targeted F-doping increases electron delocalization, and facilitates electron transfer from Ni to NiO at the nano-interfaces. This interphase synergy provides ready-to-use F-NiO active sites, allowing F-NiO/Ni@C to achieve optimum H* adsorption Gibbs free energy for HER and a lower energy barrier for UOR. As a result, the as-configured F-NiO/Ni@C || F-NiO/Ni@C cell requires an ultra-low cell voltage of 1.37 V to achieve 10 mA cm −2 in alkaline media (with 0.3 M urea), outperforming the state-of-the-art benchmark Pt/C|| RuO 2 cell (1.45 V). This study reveals the positive impact of anion doping on interphase synergy and provides useful guidelines for designing monometallic catalysts for UOR as well as hydrogen generation.
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Journal of Materials Chemistry A
·
2023
·Vol. 11
·期 15
·8248-8255
·
IF 11.9
Liang Shen,Wenhao Zhang,Yifei Feng,Jing Xu,Minghui Zhu
Hydrogenation of CO2 to produce high-value chemicals is a response to increasing environmental and energy concerns. The target products of CO2 hydrogenation, methane and CO, are both important energy sources and raw materials for the production of higher hydrocarbons. Therefore, it is very important to understand the mechanism of selectivity control of catalysts. In this work, we aim to elucidate the selectivity regulation of Zn on Ni catalysts, which has been extensively studied in the literature without reaching a consensus. We have prepared a series of catalysts with different Zn content and systematically investigated the relationship between their structural evolution and selectivity. It is found that the introduction of Zn preferentially forms an alloy with Ni and at higher loadings is present as ZnOx, which participates in the strong metal–support interaction (SMSI). The conversion of the active sites into a Ni–Zn alloy hinders further hydrogenation of the adsorbed CO intermediates and makes the catalyst CO-selective. The presence of the Ni–ZnOx interface changes the CO2 activation mechanism from an association pathway to a redox pathway.
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高影响因子
Coatings
·
2023
·Vol. 13
·期 4
·695
·
IF 3.4
Gen Li,Zhixiang Chen,Zhiwen Tan,Ran Tian,Yuantao Zhao,Lianbo Wang,Wenge Li,Yanbo Liu
The current work synthesized Ni-SiC composite coating with different SiC microparticle contents. The role of the SiC microparticle in designing the Ni-SiC composite microstructure was revealed. The SiC microparticle physically interrupted the continuous growth of the underlying columnar Ni grains. The columnar Ni grain between the embedded SiC microparticle grew without disturbance. Only upon SiC microparticles was a new layer starting with refined Ni grains observable. The vertical columnar Ni grains reappeared as the position departed the SiC microparticle upper surface. The increase in the contents of the SiC microparticle led to an increased level of grain refinement and the elimination of the (200) fiber texture. Besides that, the number of V-shaped valleys increased as well. Corrosion testing results show that the corrosion resistance of Ni-SiC composite coating increased with the increased SiC contents, which was mainly due to the optimized microstructure.Keywords:Ni matrix composite;SiC microparticles;deposits growth behavior;grain refinement;corrosion resistance
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JOURNAL OF CATALYSIS
·
2019
·
IF 7.723
Lei Yang,Shiyi Yu,Chong Peng,Xiangchen Fang,Zhenmin Cheng,Zhiming Zhou
A series of nonprecious monometallic Ni/AlSBA-15 and bimetallic Ni M (M = Zn, Ga, Cu, or Fe)/AlSBA-15 catalysts were prepared using a urea precipitation method and applied to the semihydrogenation of phenylacetylene. The catalysts were characterized by various techniques, showing that the Ni particle size of catalyst can be tuned by adjusting the Al content, and NiZn and NiGa supported catalysts exhibited geometric and electronic effects that originated from the bimetallic alloy. Among all the catalysts studied, NiZn 3 /AlSBA-15, with a turnover frequency of 10.89 s −1 comparable to that of precious Pd-based catalysts, presented the highest selectivity to styrene (90.3%) at nearly 100% conversion of phenylacetylene in semibatch operation. This catalyst was further evaluated in a continuous fixed-bed reactor for semihydrogenation of a model C 8 aromatic fraction of pyrolysis gasoline (a mixture of phenylacetylene, styrene, ethylbenzene and xylene), which aimed at assessing its practical application of recovering styrene from pyrolysis gasoline. The results showed that at complete conversion of phenylacetylene, the styrene concentration in the product was always kept at a stable level and higher than its initial concentration over 100 h of time on stream, demonstrating high selectivity and good stability of NiZn 3 /AlSBA-15. Finally, the application of NiZn 3 /AlSBA-15 was extended to other phenylacetylene derivatives.
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IET Renewable Power Generation
·
2019
·Vol. 13
·期 10
·1641-1646
·
IF 3.605
Xiangping Li,Jianguang Zhang,Ningge Xu,Guanyi Chen,Beibei Yan
With the depletion of non-regenerated energy and the increasing awareness of environmental protection, renewable energy developing has become a key subject of research. Hydrogen as a kind of clean energy has aroused much attention. In this study, hydrogen production from bio-oil derived phenolic compound in aqueous phase was studied. Hydrotalcite-derived Ni/Zn/Al catalysts with different metallic compositions were synthesised and screened for aqueous-phase reforming (APR) of phenol. The physiochemical characterisations of hydrotalcite-derived Ni/Zn/Al samples were detected by X-ray powder diffraction (XRD), scanning electron microscope (SEM), fourier transform infrared spectroscopy (FTIR) and N 2 -sorption. In the calcined hydrotalcite-derived Ni 5.3 /Zn 2.7 /Al samples, most of the metal oxides exist in the form of rock solid and wurtzite type phase. In order to optimise the reaction condition of APR of phenol, the impacts of initial phenol concentration, reaction pressure and reaction temperature during the APR of phenol were investigated. It was found that increasing the concentration of phenol could enhance the side reaction and decrease the selectivity of hydrogen, while enhancing the reaction pressure was not favourable for hydrogen production. Moreover, proper reaction temperature was necessary for APR of phenol to produce hydrogen over hydrotalcite-derived Ni/Zn/Al catalysts.
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INORGANIC CHEMISTRY
·
2018
·
IF 4.7
Fan Sun,Zhongnan Guo,Ning Liu,Dan Wu,Jiawei Lin,Erjian Cheng,Tianping Ying,Shiyan Li,Wenxia Yuan
In this work, we report the discovery of a new Ni-based quasi-one-dimensional selenide: Cs0.9Ni3.1Se3. This compound adopts the TlFe3Te3-type structure with space group P63/m, which consists of infinite [Ni3Se3] chains with face-sharing Ni6 octahedra along the c direction. The lattice parameters are calculated as a = 9.26301(4) Å and c = 4.34272(2) Å, with the Ni–Ni distance in the ab plane as 2.582(3) Å, suggesting the formation of a Ni–Ni metallic bond in this compound. Interestingly, it has been found that Cs0.9Ni3.1Se3 is nonstoichiometric, which is different from the other TlFe3Te3-type phases reported so far. Structure refinement shows that the extra Ni atom in the structure may occupy the 2c site, together with Cs atoms. Cs0.9Ni3.1Se3 shows metallic behavior with monotonously decreased resistivity with temperatures from 300 to 0.5 K. Measurements on the magnetic susceptibility display a spin-glass state below 7 K. The specific heat curve gives a Sommerfeld coefficient of 14.6 mJ·K–2·mol–1 and a Debye temperature of 143.6 K. The discovery of this new compound enriches the diversity of low-dimensional materials in a transition-metal-based family and also sheds light on the structure–property relationship of this system.
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高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2018
·
IF 4.229
Bin Li,Baohua Zhang,Qingqing Guan,Shanshuai Chen,Ping Ning
An effective Ni/CeO 2 catalyst prepared by the polyol reduction method for degrading phenol into CH 4 , H 2 and CO 2 in supercritical water (SCW) was developed. About 80% carbon gasification efficiency can be achieved at 525 °C and 60 min with 5 wt% phenol, 0.098 kg/m 3 water density and 0.5 g Ni/CeO 2 /g phenol catalyst, forming CH 4 and H 2 as the main gaseous products. Comparison study indicated that the efficiency of present Ni/CeO 2 catalyst was about 20% higher than that of a commercial catalyst, i.e., Ni/SiO 2 Al 2 O 3 from Sigma-Aldrich with 65 wt%Ni, at a reaction conditions of 500 °C and 30 min. The characterization analyses of BET, TPR, XRD , XPS and TEM indicated that there was a NiCe alloy formed in Ni/CeO 2 , which could be important to enhance the activities of the carbon gasification efficiencies and gas yields. A kinetic modelings were conducted and the results showed that the lnA and the activation energy (Ea) of gasification were 7.1 ± 0.5 and 58.1 ± 3.2 kJ/mol for the gaseous product, and were 2.6 ± 0.9 and Ea is 36.6 ± 5.6 kJ/mol for the char formation , respectively. The present Ni-based-metal Ni/CeO 2 catalyst is cheaper and has a potential application for the gasification to convert phenol into gases fuels in SCW process.
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Materials Research Express
·
2019
·Vol. 6
·期 9
·096433
·
IF 1.449
Baosong Li,Shengsong Du,Tianyong Mei
Ni-Cu/TiN-ZrO2 nanocomposite coating was pulse electrodeposited by incorporation of Cu, TiN and ZrO2 simultaneously in Ni deposits from a citrate bath in the presence of additives. The surface morphology, structural and electrochemical properties of Ni-Cu/TiN-ZrO2 nanocomposite coating were evaluated. Results illustrated that the nanocomposite coating exhibits nodular-like structure with aggregated granules dispersed on its surface. The anti-corrosion performance of Ni-Cu deposits could be reinforced much by incorporation of TiN-ZrO2 nanoparticles. The surface of the coating contains Ni, Cu, Ti, Zr, O and C elements and indicates the formation of the oxide layer. The corrosion resistance of the nanocomposite coating is not only dependent on the current density and duty cycle, but also their combination. The Ni-Cu/TiN-ZrO2 nanocomposite coating electrodeposited at duty cycle of 70% and current density of 4 A dm−2 has the highest anti-corrosion performance. In comparison with duty cycle and current density, the effect of frequency on corrosion resistance is not much.
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