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JOURNAL OF WUHAN UNIVERSITY OF TECHNOLOGY-MATERIALS SCIENCE EDITION · 2021 ·Vol. 36 ·期 2 ·174-182 · IF 0.957

Ceramification of Composites of MgO-Al3O3-SiO2/Boron Phenolic Resin with Different Calcine Time

Shi Minxian,Tang Qingxiu,Fan Shanshan,Dong Chuang,Huang Zhixiong

The ceramifiable polymer composite of MgO-Al 2 O 3 -SiO 2 /boron phenolic resin(MAS/BPF) with 40wt% of inorganic fillers was calcined at 1 200 °C for different time to promote ceramification of ceramifiable composite and improve heat resistance. The effects of different calcine time on the macroscopical morphology, mass loss, phase evolution, microstructure and chemical bond evolution of MAS/BPF composites were characterized by XRD, XPS, and SEM analyses. The experimental results reveal that the increase of calcine time result in the fewer holes, relatively denser and smoother top layer of MAS/BPF composites and protect the interior from deeper decomposition. The final residues of composites are amorphous carbon and C-O-Si-Al-Mg ceramic. And MAS/BPF composites show excellent mass stability, low shrinkage and self-supporting features after 2 h holding compared with BPF composites without 40wt% of inorganic fillers.

研究领域: 材料科学 · 无机化学
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ACS Applied Materials & Interfaces · 2020 · IF 8.758

Low-Temperature Methane Oxidation Triggered by Peroxide Radicals over Noble-Metal-Free MgO Catalyst

Ying-juan Hao,Li-gang Tian,Erhong Duan,Jixing Liu,Tian-yuan Qi,Wei-qi Kong,Xue-han Qi,Xinying Liu,Ying Liu,Jun Zhao,Fa-tang Li

Methane is a greenhouse gas that contributes to global warming. Hence, effectively removing the low concentration (<1000 ppm) of methane in the environment is an issue that deserves research in the field of catalysis. In this study, oxygen–magnesium bivacancies are simultaneously imbedded into MgO by designing an in situ reduction combustion atmosphere for oxygen release and substituting magnesium with carbon to induce the formation of magnesium vacancies. The DFT calculations reveal that the surface electron density of MgO is improved by the oxygen vacancy structure and the substitution of Mg by C in bulk; this accelerates migration of the charge from the material surface to the adsorbed oxygen species, which leads to abundant surface peroxide species that enable activation and oxidation of methane at a low temperature (below 200 °C). This work could provide a concept for developing non-noble or transition metal oxides for low-temperature activation and conversion of alkanes in the thermocatalytic field through reactive oxygen species.

研究领域: 催化化学 · 环境科学 · 材料科学
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MEASUREMENT SCIENCE and TECHNOLOGY · 2025 ·Vol. 36 ·期 3 ·035110 · IF 3.4

Synthesis of highly selective mesoporous MgO nanoparticles for efficient detection of trace isobutyraldehyde

Qianchun Zhang,Chengcheng Wan,Jiumei He,Zhaoru Ban,Shan Tang,Li Jiang,Yanju Chen,Xixi Long

In this study, mesoporous MgO nanoparticles were successfully synthesized using carbon quantum dots as templates and an outstanding cataluminescence sensor system was established based on these nanoparticles. In a particular situation, the constructed sensor demonstrated remarkable linear range was 0.3106–310.6 ppm (R2 = 0.9990) with a low limit of detection of 0.0994 ppm and a signal-to-noise ratio (S/N) of 3. The mesoporous MgO nanoparticle sensor was utilized to analyze the isobutyraldehyde content in real samples. Outstanding recoveries were achieved within range of 83.4%–111%, with the relative standard deviations (n = 7) ranging from 2.0% to 8.2%. Moreover, the 35 d test results showed that the sensor has good stability. Density functional theory and gas chromatography-mass spectrometry were used to research the mechanism of the designed cataluminescence sensor. This work presents a universal methodology for constructing isobutyraldehyde gas sensors with high sensitivity and selectivity, and mesoporous MgO nanoparticles sensors that expand the applications available in the industry and environment analysis.

研究领域: 材料科学 · 环境分析化学
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Journal of Environmental Chemical Engineering · 2021 · IF 5.909

Insights into enhancement of photocatalytic properties of g-C3N4 by local electric field induced by polarization of MgO(111)

Zanling Huang,Xia Zhao,Hong Xia,Fushen Lu,Liangsheng Hu,Paul K. Chu

Photocatalysis has attracted worldwide attention in the fields of energy storage and environmental remediation. However, the solar-to-energy conversion efficiency is still low due to fast charge carrier recombination in the bulk phase of conventional photocatalysts. Herein, a series of photocatalysts including g-C 3 N 4 (GCN), non-polar MgO(110)/GCN composite, MgO(110)+GCN mixture, polar MgO(111)/GCN composite, and MgO(111)+GCN mixture are prepared and their photocatalytic activities are investigated systematically. The polar and non-polar MgO improve the photocatalytic properties of GCN in the following order: MgO(111)+GCN>MgO(110)/GCN>MgO(111)/GCN>MgO(110)+GCN>GCN. Benefiting from charge carrier separation rendered by the local electric field (LEF) induced by MgO(111) polarization, MgO(111) improves the performance of GCN significantly when it is mixed with GCN. However, the enhancement effects are reduced when it is combined with or integrated into GCN as in the MgO(111)/GCN composite, where the traditional heterojunction effect constitutes the main enhancement mechanism. Our study reveals that the photocatalytic enhancement by the LEF effect is superior to that by the traditional heterojunction effect based on polar supporting materials. Our results offer insights into the enhancement mechanism of photocatalysts with polar supporting materials and reveal a simple strategy to optimize photocatalytic processes to exploit solar energy efficiently.

研究领域: 材料科学 · 能源与环境科学
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SOLAR ENERGY MATERIALS AND SOLAR CELLS · 2024 · IF 6.3

Structure-activity relationship between pore morphology and thermochemical energy storage properties based on MgCO3/MgO

Y.X. Xu,C.Y. Zhao

Thermochemical energy storage (TCES) is a pivotal technology for addressing the space-time mismatches in energy supply and demand. MgCO 3 /MgO carrier offers the advantages of high energy density , seasonal storage capability, and abundant nontoxic reserves. However, it is encumbered by poor exothermic activity and kinetic irreversibility . In this study, innovative preparation approaches for MgCO 3 /MgO have been developed, involving the regulation of physical morphology, so as to reveal the structure-activity relationship between pore morphology and TCES properties. The results indicate that SD-cotton-MgO (MgO prepared by structure-directing agent, cotton) could carbonate up to 76.98 %, facilitated by its mesopores that aid in the transport of reactants. SGSC-MgO (MgO prepared by sol-gel self-combustion method) exhibits the fastest reaction rate at the initial stage, with a rate of 593.1 μmol/min/g adsorbent because distributed macropores expose the other nanopores . As for SD-CPM-MgO (MgO prepared by structure-directing agent, carboniferous polysaccharide microsphere), owning to long pore distance of micropores hindering CO 2 diffusion, its kinetics gradually decreases as the CPM size decreases. Porous media with mixed aperture could exhibit strong kinetic performance. Furthermore, the heat storage density and maximum power of SD-cotton-MgO increase as the endothermic temperature rises, achieving a peak energy density of 1385.7 kJ/kg MgCO 3 at 400 °C. Still, its heat release density increases and then decreases with exothermic temperature, reaching 1964.3 kJ/kg MgO at 320 °C. Finally, the cycle stability is contingent on the activation of the chemical modification for the first heat release and antidegradation of the physical structure for subsequent cycles. SD-cotton-MgO doped with Na 0.5 K 0.5 NO 3 maintains at 50 % after 30 cycles, exhibiting no collapse or agglomeration due to its robust porous structure with strong thermal stability and permeability.

研究领域: 材料科学 · 能源存储
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CERAMICS INTERNATIONAL · 2018 · IF 3.057

Template-free synthesis of MgO mesoporous nanofibers with superior adsorption for fluoride and Congo red

Zhichao Yu,Chonghe Xu,Kangkang Yuan,Xinzhu Gan,Haifeng Zhou,Xinqiang Wang,Luyi Zhu,Guanghui Zhang,Dong Xu

MgO mesoporous nanofibers were obtained by a template-free electrospinning method. The unique bumpy-structure was obtained on the surface of nanofibers that could enhance the surface area and provide more active sites for adsorption. The formation mechanism of the bumpy-structure has been investigated. The as-prepared MgO nanofibers with a high surface area of 194.17 m 2 g −1 exhibited excellent adsorption capacities for fluoride of 237.49 mg g −1 . Furthermore, the MgO nanofibers showed selective adsorption for different organic dyes and have superior adsorption capacity for Congo red (4802.27 mg g −1 ). The adsorption processes for both fluoride and Congo red were systematically investigated, which were found to follow the pseudo-second-order kinetic model. By comparison with the reported fabrication routes and adsorption capacities of mesoporous MgO, the synthesis process is simple, controllable and template-free, and the superior adsorption performance provided a potential adsorbent for the removal of fluoride and Congo red in wastewater treatment. The high surface area of the MgO mesoporous nanofibers might also promote its application in basic catalysis and other fields.

CAS / MDL: 25249-54-1 9003-39-8
研究领域: 材料科学 · 环境科学
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CERAMICS INTERNATIONAL · 2025 · IF 5.6

Fabrication and properties of lasing grade Nd:Y2O3 transparent ceramics with ZrO2 and MgO additives

Yongzhi Luo,Bin Wang,Xi Zhang,Bin Kang,Jianguo Deng,Shengquan Yu

Nd:Y 2 O 3 transparent ceramics were fabricated by vacuum pre-sintering and post-hot isostatic pressing with ZrO 2 and MgO as sintering additives. It was found that binary additives not only promoted the densification of Y 2 O 3 ceramics, but also decreased the pre-sintering temperature by at least 150 °C compared with the single addition of ZrO 2 . The best quality sample with 1 at.% ZrO 2 and 0.06 at.% MgO was pre-sintered at 1550 °C and post-HIPed at 1500 °C. The average grain size was approximately 0.96 μm, and the in-line transmittance reached 75.9 % at 400 nm and 81.4 % at 1000 nm. The ceramic also exhibits good optical homogeneity, which is evaluated by the interference stripes with the PV and RMS values of 385.8 nm and 21.3 nm, respectively. Continuous wave laser operation of the sample was demonstrated, and a maximum output power of 1.73 W at 1080.4 nm was achieved with a slope efficiency of 11.3 %.

CAS / MDL: 1314-23-4
研究领域: 材料科学 · 光学工程
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ACS Applied Materials & Interfaces · 2024 · IF 8.3

Highly Concentrated Electrolyte Superlubricants Enhanced by Interfacial Water Competition Around Chemically Active MgO Additives

Hongyu Liang,Shijing Zou,Manqiang Liu,Tianqiang Yin,Xiaojie Xia,Xijun Hua,Yonghong Fu,Yongfeng Bu

The low concentration of water-based lubricants and the high chemical inertness of the additives involved are often regarded as basic norms in the design of liquid lubricants. Herein, a novel liquid superlubricant of an aqueous solution containing a relatively high concentration of salt, lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), is reported for the first time, and the superlubricity stability and load-bearing capacity of the optimized system (MgO0.10/LiTFSI10) are effectively strengthened by the addition of only trace (0.10 wt %) water–chemically active MgO additives. It demonstrates higher applicable loads, lower COF (∼0.004), and stability relative to the base solution. Only a trace amount of MgO additive is needed for the superlubricity, which makes up for the cost and environmental deficiencies of LiTFSI10. The weak interaction region between free water and the outer-layer water of Li+ hydration shells becomes a possible ultralow shear resistance sliding interface; the Mg(OH)2 layer, generated by the reaction of MgO with water, further creates additional weakly interacting interfaces, leading to the formation of an asymmetric contact between the clusters/particles within the hydrodynamic film by moderating the competition between interfacial water and free water, thus achieving high load-bearing macroscopic superlubricity. This study deepens the contribution of electrolyte concentration to ionic hydration and superlubricity due to the low shear slip layer formed by interfacial water competition with water-activated solid additives, providing new insights into the next generation of high load-bearing water-based liquid superlubricity systems.

CAS / MDL: 90076-65-6 7782-42-5
研究领域: 材料科学 · 化学工程
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JOURNAL OF SOL-GEL SCIENCE AND TECHNOLOGY · 2012 ·Vol. 63 ·期 3 ·495-500 · IF 1.632

In situ sol–gel preparation of high transparent fluorinated polyimide/nano-MgO hybrid films

Lu Junwen,Wang Wei,Zhang Aiqing,Tan Fatang,Qiao Xueliang

Hybrid nanocomposite films of magnesium oxide (MgO) in fluorinated polyimide (PI) from 4, 4′-(hexafluoroisopropylidene) diphthalic anhydride (6FDA) and 4, 4′-Diaminodiphenyl ether (ODA) have been successfully fabricated via an in situ sol–gel polymerization technique. The MgO content in hybrid films was varied from 0 to 5 wt%. The hybrid films were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), ultraviolet–visible (UV–Vis) spectroscopy and thermal gravimetric analyses (TGA). The results of FTIR, XRD and FESEM showed that the MgO nanoparticles were well dispersed in the polymer matrix due to the coordination between the carbonyl group of polymers and Mg atom, and the as-prepared hybrid films exhibited excellent optical transparency in the visible region and good UV-shielding properties in the UV region. Although the thermal stability of the hybrid films is slight inferior to pure PI, it is still good for the practical application below the temperature of 300 °C.

CAS / MDL: 2414-98-4
研究领域: 材料科学 · 化学工程
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ENERGY CONVERSION AND MANAGEMENT · 2015 · IF 4.38

Selective cyclohexanol production from the renewable lignin derived phenolic chemicals catalyzed by Ni/MgO

Jinxing Long,Shiyang Shu,Qingyun Wu,Zhengqiu Yuan,Tiejun Wang,Ying Xu,Xinghua Zhang,Qi Zhang,Longlong Ma

Selective production of cyclohexanol from renewable lignin derived phenolic has been presented using the cost-efficient catalyst Ni/MgO which shows excellent catalytic activity in the hydrogenation reaction and dehydroxylation inhibition. Guaiacol, one of the most abundant lignin depolymerization products, was selected as the model compound. The hydrogenation performance of guaiacol was investigated over various catalysts. The effect of the reaction parameters was also studied. The results showed that guaiacol could be efficiently converted to cyclohexanol, which is a highly value-added precursor and additive for bio-fuel that is generally obtained from unsustainable fossil resources. Under the mild condition (160   °C, 3   h and 3   MPa H 2 ), more than 97.74% of guaiacol conversion with 100% cyclohexanol selectivity can be achieved in the presence of 20% Ni/MgO. Intensive catalyst characterization demonstrated that the efficient promotion effect of the base carrier for the Ni active center was responsible for efficient guaiacol conversion and selective cyclohexanol production. Furthermore, the Ni/MgO catalyst showed excellent recyclability, where no significant activity loss was observed even after four runs. Moreover, the reaction pathway and the catalytic mechanism are proposed.

研究领域: 化学工程 · 催化科学 · 可再生能源
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JOURNAL OF IRON AND STEEL RESEARCH INTERNATIONAL · 2025 · IF 3.6

Preparation and microstructure regulation of MgO–CaO–Y2O3 refractories with enhanced slag resistance

Jin Hu-lin,Ma Yan,Wang Zhou-fu,Liu Hao,Dong Yun-jie,Yi Nian,Wang Xi-tang,Deng Cheng-ji,Xia Zhong-feng,Quan Zheng-huang,Zhang Ling,Tong Guang-da,Fu Wei-dong

MgO–CaO refractories have attracted much attention in the field of clean steel due to the ability of their internal CaO to adsorb elements such as S and P in molten steel. However, there are still some problems such as difficult sintering and insufficient corrosion resistance existing in this system. Different contents of Y 2 O 3 were introduced into MgO–CaO system to prepare MgO–CaO–Y 2 O 3 ternary refractories via traditional and induction sintering methods. The influence of microstructural regulation on the slag-resistant properties of the refractories was investigated. The results show that the introduction of Y 2 O 3 in the MgO–CaO refractories prepared via the two sintering methods leads to the grain boundary reconstruction effect. Under the condition of traditional sintering, when a smaller amount of Y 2 O 3 is introduced into the MgO–CaO refractories, Y 2 O 3 is able to activate the lattice, promote sintering, and improve the densification of the refractories. However, when more Y 2 O 3 is introduced, the excess Y 2 O 3 hinders the sintering densification process. Combined with lamellar intergranular phase generated in the refractories, Y 2 O 3 -based solid solution can react with the slag, increase the slag viscosity and inhibit the penetration of the slag into the refractories. Under the condition of induction sintering, the solid solution of yttrium ions in CaO is increased by using the coupling of electromagnetic and thermal fields. Compared with the MgO–CaO refractories with high Y 2 O 3 content prepared by traditional sintering, the induction sintered refractories have higher densification, which further increases the corrosion resistance. The results provide a new path for developing long-life MgO–CaO based refractories.

CAS / MDL: 13494-98-9
研究领域: 材料科学 · 陶瓷 · 冶金 · 耐火材料技术
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SCRIPTA MATERIALIA · 2019 · IF 4.539

Fabrication and densification mechanism of MgO/Graphene composites with LiF as additive

Nan Lu,Gang He,Zengchao Yang,Yong Li,Jiangtao Li

MgO/Graphene composites were prepared by combustion synthesis (CS) followed with spark plasma sintering (SPS) using LiF as sintering additive. The densification mechanism of MgO/Graphene composites doped with LiF was systematically investigated. With incorporating small amount of graphene into MgO , the spectral absorptivity of the composite was improved, whereas the density, hardness and average grain size were decreased. The densification of submicron sized MgO/Graphene ceramics was realized by the balance between sintering promoted by LiF and grain refinement of graphene.

研究领域: 材料科学 · 陶瓷工程
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