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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2022 ·Vol. 33 ·期 26 ·20981-20991 · IF 2.779

Correlation between phase structure and polarization of Mg doped (Ba0.98Li0.02)TiO3 energy storage ceramics

Yan Gui-wei,Liu Qing-qing,Fang Bi-jun,Chen Zhi-hui

Mg doped (Ba 0.98 Li 0.02 )TiO 3 energy storage ceramics with antiferroelectric-like double hysteresis loops were prepared using solid-state reaction method. XRD patterns indicated that tetragonal phase structure of the pure (Ba 0.98 Li 0.02 )TiO 3 ceramic was destroyed and the orthorhombic phase structure appeared with Mg doping. The ratio of orthorhombic/tetragonal phase increased with Mg content increasing, and the value of polarization was in direct proportion to the ratio of orthorhombic/tetragonal phase. The breakdown strength of (Ba 0.98 Li 0.02 )(Mg x Ti 1− x )O 3 ceramics was improved from 60.97 kV/cm at x  = 0 to 103.66 kV/cm at x  = 0.04. The optimum energy storage properties of (Ba 0.98 Li 0.02 )(Mg x Ti 1− x )O 3 ceramics were obtained with energy storage density of 0.76 J/cm 3 at 102.5 kV/cm when x  = 0.04, which is nearly 2.3 times larger than the pure (Ba 0.98 Li 0.02 )TiO 3 ceramic, and the energy storage efficiency was improved from 64 to 87%.

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JOURNAL OF HAZARDOUS MATERIALS · 2021 · IF 10.588

Spontaneous nutrient recovery and disinfection of aquaculture wastewater via Mg–coconut shell carbon composites

Xiongjian Chen,Yanchao Jin,Zijing Zhou,Peiwen Huang,Xiao Chen,Rui Ding,Riyao Chen

Aquaculture wastewater contained large amounts of pathogenic microorganisms , nitrogen (N) and phosphorus (P). In this study, the nutrient recoveries and wastewater disinfection were simultaneously achieved using Mg–coconut shell carbon (Mg–CSC). The composites were prepared by a ball milling method. The hydrogen peroxide (H 2 O 2 ) was in-situ generated by the dissolved oxygen reduction driven by Mg corrosion on the CSC surface, which inactivated the microorganisms . Besides that, Mg corrosion provided sufficient Mg ions and appropriate pH conditions for struvite formation. The results show that 5.4-log E.coli removal was achieved under different conditions. Improving the Mg/CSC ratio and composite dosage could shorten the time required for disinfection. In addition to H 2 O 2 , singlet oxygen played a critical role. Reactive oxygen species destroyed the cellular structure and killed the bacteria. The recoveries of NH 4 + - N NH4+-N and P under certain conditions were about 60% and 91%, respectively. An increased composite dosage could improve the recovery ratio of P. Excessive dosages were not beneficial for removing NH 4 + - N NH4+-N . The characterization result revealed that struvite crystals were the main precipitates on the CSC surface. The Mg–CSC composites also revealed satisfied nutrient recovery and disinfection performances in the real aquaculture wastewater treatment process .

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SEPARATION AND PURIFICATION TECHNOLOGY · 2021 · IF 7.312

Capacitive deionization of NaCl solution with hierarchical porous carbon materials derived from Mg-MOFs

Chun-Ping Li,Ya-Qi Wu,Fei-Yang Zhang,Li-Xin Gao,Da-Quan Zhang,Zhong-Xun An

Carbon materials with suitable pore size distribution, high specific surface area and good wettability are crucial for the capacitive deionization (CDI) electrode. Herein, the Mg-MOF-74 derived carbon (MMCK) is prepared by solvothermal synthesis, carbonization, and potassium hydroxide (KOH) activation method. The MMCK has super hydrophilicity and rich hierarchical porous structure composed of micropores, mesopores and macropores. The capacitive deionization of MMCK is investigated in NaCl aqueous solution. The MMCK has high oxygen doping amount, and has a high electrosorption capacity (16.82 mg·g −1 ) for 500 mg·L −1 NaCl. This indicates that MMCK is novel and potential material for capacitive deionization.

CAS / MDL: 610-92-4
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Journal of Magnesium and Alloys · 2021 · IF 10.088

Catalytic mechanism of in-situ Ni/C co-incorporation for hydrogen absorption of Mg

Bogu Liu,Bao Zhang,Haixiang Huang,Xiaohong Chen,Yujie Lv,Zhongyu Li,Jianguang Yuan,Ying Wu

Ni and carbon materials exhibit remarkable catalysis for the hydriding reaction of Mg. But the underlying mechanism of Ni/C hybrid catalysis is still unclear. In this work, density functional theory (DFT) calculation is applied to investigate the effect of Ni/C co-incorporation on the hydriding reaction of Mg crystal. The morphology and crystal structure of the Ni/C co-incorporated Mg sample show that the co-incorporated structure is credible. The transition state searching calculation suggests that both the incorporations of Ni and C are beneficial for the H 2 dissociation. But Ni atom has a dramatic improvement for H 2 dissociation and makes the H diffusion become limiting step of the hyriding reaction. The Ni d z 2 orbit and H s orbit accept the electrons and combine together compactly, while the Ni d xy orbit is half-occupied. The catalytic effect of Ni on H 2 dissociation can be ascribed to the bridging effect of Ni d xy orbit. The incorporation of C can weaken the over-strong interaction between Ni and H which hindered the H diffusion on Mg(0001). The Ni/C co-incorporated Mg(0001) shows the best performance during hyriding reaction compared with the clean and single incorporated Mg(0001).

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RARE METALS · 2021 ·Vol. 40 ·期 9 ·2538-2551 · IF 4.003

Photothermal-controlled sustainable degradation of protective coating modified Mg alloy using near-infrared light

Han Zhi-Xin,Liu Xiang-Mei,Tan Lei,Li Zhao-Yang,Zheng Yu-Feng,Yeung Kelvin Wai-Kwok,Cui Zhen-Duo,Liang Yan-Qin,Zhu Sheng-Li,Wu Shui-Lin

Abstract Controlling the corrosion rate is critical for practical applications of Mg-based alloys. In this work, we constructed a protective coating of hybrid polycaprolactone (H-PCL)/indocyanine green (ICG) on AZ31 Mg alloy, whose degradation rate was controlled by 808-nm near-infrared (NIR) light irradiation. The corrosion behaviors of H-PCL/ICG coated Mg alloys were systematically investigated by potentiodynamic polarization tests, electrochemical impedance spectroscopy (EIS) and hydrogen evolution experiments. The results disclosed that the H-PCL/ICG composite coating could effectively protect Mg alloy from corroding without NIR light irradiation. In contrast, under 808-nm NIR light irradiation, the corrosion resistance of this composite coating was decreased significantly, i.e., the corrosion current density ( i corr ) increased from (8.81 ± 1.068) × 10 −8 to (1.22 ± 0.545) × 10 −6 A·cm −2 . This is because the component of ICG in the coating was excited to produce heat locally, which triggered the glass transition temperature ( T g ) of H-PCL in the coating, resulting in the motion of the molecular chain segment. Consequently, the electrolytes penetrated the coating and corroded the Mg substrate. In vitro biological experiment indicated that the synthesized coating exhibited good cytocompatibility. Hence, these findings will provide a new strategy for designing novel photoresponsive coatings to remotely adjust the degradation rate of biodegradable metals for biomedical applications. Graphic abstract

CAS / MDL: 3599-32-4
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JOURNAL OF MATERIALS ENGINEERING AND PERFORMANCE · 2021 ·Vol. 30 ·期 2 ·1567-1576 · IF 1.819

Mg(ClO4)2-N,N-Dimethylformamide (Acetonitrile)/NaCl Double Electrolytes for Magnesium–Air Batteries

Ma Jingling,Jia Xingliang,Ma Mingsheng,Zhang Chenfei,Ren Fengzhang,Wang Guangxin

To limit corrosion and retain activity of magnesium anode, magnesium–air batteries with double solutions: 0.5 M Mg(ClO 4 ) 2 - N , N -dimethylformamide (DMF)/0.6 M NaCl-H 2 O, 0.5 M Mg(ClO 4 ) 2 –acetonitrile (AN)/0.6 M NaCl-H 2 O are prepared. Cathodic and anodic reactions proceed in inorganic and organic solutions separately. Discharge performance, discharge morphology, and corrosion behavior of magnesium anode are researched. Results obtained show that organic electrolytes separate anode from the aqueous electrolyte, thus improving anode utilization rate. Due to 0.6 M NaCl solution used in air cathode side, the batteries show higher discharge voltages. A better discharge performance has been observed in double electrolytes at 1 mA·cm −2 discharge. Results of discharge morphology and electrochemical impedance spectroscopy agree well with discharge performance. The discharge mechanism of magnesium anode in different solutions is also discussed.

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MATERIALS TECHNOLOGY · 2020 · IF 1.738

Microstructure and electromagnetic properties of Nd3+substitued Mg-Mn nanocrystalline ferrites via hydrothermal procedure

Huan Yang,Renxin Xu,Yaohui Zhao,Jian Cai

Mg0.2Mn0.8NdxFe2-xO4 (x = 0.000, 0.025, 0.050, 0.075 and 0.010) nano crystalline is synthesized via hydrothermal technique. Single cubic spinel phase is confirmed by XRD and the formation of Mg0.2Mn0.8NdxFe2-xO4 is verified by EDS. The average size of the nanoferrites is examined by TEM image. Nd3+ substituted Mg-Mn nanoferrites exhibit the low saturation magnetization (Ms) and high coercivity (Hc). The ferrite composites present that the resistivity and the magnetic loss are less than 2.8×107 Ω·cm and 0.75 in the range of 2-18 GHz, respectively. The optimized Mg0.2Mn0.8NdxFe2-xO4 (x=0.050) showed the minimum reflection loss of -39.80 dB at 1.4 GHz and effective absorption bandwidth (lower than -10 dB) of 7.58 GHz with a thickness of only 3 mm. The high coercivity, resistivity and excellent wave absorption performance indicate that the addition of Nd3+ contributes to the synthesis of the excellent soft magnetic materials and wave absorbing materials.

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ACS Applied Materials & Interfaces · 2020 · IF 8.758

Superhydrophobic ZIF-8-Based Dual-Layer Coating for Enhanced Corrosion Protection of Mg Alloy

Xingxing Yin,Peng Mu,Qingtao Wang,Jian Li

Magnesium (Mg) and its alloys are regarded as the most promising engineering materials because of their unique property. However, the Mg alloys were easily corroded in humid environments, which restricted their wider applications. Herein, the superhydrophobic ZIF-8/PVDF/LDH (SZPL) double-layered coating was fabricated on Mg alloys via electrodeposition and dip-coating methods, which consisted of the underlying layered double hydroxide (LDH) transition structure and top superhydrophobic zeolitic imidazolate framework-8 (ZIF-8) layer. Besides, the LDH transition structure not only worked as a protection shield but also strengthened the binding force between the substrate and the top superhydrophobic ZIF-8 layer. The top superhydrophobic ZIF-8 layer could serve as an armor on the LDH layer to further prevent the corrosive ions from infiltrating the microporous defects. In addition, the as-prepared SZPL double-layered coating showed robust superhydrophobic and self-cleaning properties, which could block the electrolyte invasion. Furthermore, the electrochemical tests demonstrated that the SZPL coating highly enhanced the corrosion protection ability of Mg alloys. Moreover, the superhydrophobic ZIF-8-based coating could still retain excellent anticorrosion property after immersion in 3.5 wt % NaCl solution for 7 days. The enhanced anticorrosion ability was ascribed to the fact that a synergistic effect of the underlying LDH transition layer hindered the transmission of aggressive ions and the top superhydrophobic ZIF-8-based coating decreased the contact area of the substrate with corrosive solution. Therefore, such coatings offer a new strategy for fabricating excellent anticorrosive coatings with robust superhydrophobicity and self-cleaning performance on metal substrates.

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CATALYSIS LETTERS · 2019 ·Vol. 150 ·期 6 ·1591-1604 · IF 2.372

Ni–Mg–Al Catalysts Effectively Promote Depolymerization of Rice Husk Lignin to Bio-Oil

Du Boyu,Chen Changzhou,Sun Yang,Liu Bingyang,Yang Yingying,Gao Si,Zhang Zhenshu,Wang Xing,Zhou Jinghui

Abstract Catalytic depolymerization of lignin to produce bio-oil, liquid fuels, and aromatic chemicals in high yields is important for a biorefinery to remain competitive. In this study, undoped and Ni-doped catalysts for depolymerization of rice husk lignin (RHL) were developed and analyzed. The results showed that the catalysts had hydrotalcite-like structures with lamellar morphology. With suitable Ni-doping amount, the catalysts had high activity, thus better promoted the depolymerization of RHL. Among all catalysts, the Ni1/4MgAl catalyst could best promote the cleavage of the β-O-4 aryl ether bond in RHL molecule and thus could substantially increase the yields of bio-oil. The depolymerization catalyzed by this catalyst was also found to be temperature-, time-, and solvent-dependent. This study provides information that can be beneficial to the biorefinery industries and may help promote the valorization of lignin. Graphic Abstract

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ACS Sustainable Chemistry & Engineering · 2019 · IF 6.97

Domino Reactions for Biofuel Production from Zymotic Biomass Wastes over Bifunctional Mg-Containing Catalysts

Cai Wu,Chun Shen,Yahui Gong,Jie Wang

The shortage of fossil resources and strict environmental regulations have ignited great efforts in the production of bio-based fuels and chemicals via biorefinery. Herein, considering the strong interaction between Ni and Mg species, we specially designed and prepared Ni/CaMgO and Ni/MgSiO for alkylation and hydrodeoxygenation (HDO) reactions during the upgrading of the acetone–butanol–ethanol (ABE) fermentation mixture. Gratifyingly, the Mg-decorated catalysts exhibited great catalytic performance: a selectivity of 63.9% under a conversion of 94.2% was achieved for C8–C15 ketones and alcohols, which is higher than that over other heterogeneous alkali-based catalysts, and the obtained mixture was completely converted into the corresponding alkanes at 190 °C (H2 pressure: 1 MPa). It is worth noting that jet fuels or gasoline could be efficiently and selectively obtained by facile adjustment of the composition of the ABE fermentation product. Moreover, investigation on the structure–activity correlation confirmed that the outstanding activity of Ni/MgSiO for HDO could be attributed to the synergic catalysis between Ni0 and strong acid sites. The Ni/CaMgO and Ni/MgSiO catalysts reported in this work offer three advantages: selectively upgrading zymotic biomass wastes into biofuels, replacing the expensive noble metal (Pd) by the base metal (Ni), and realizing the HDO process under mild conditions and complying with the principles of “green chemistry”. Overall, this work opens a new possibility for biofuel production, which is conductive to the rational design and implementation of highly active heterogeneous catalysts.

CAS / MDL: 112926-00-8
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Advanced Healthcare Materials · 2024 · IF 10

Citrate Improves Biomimetic Mineralization Induced by Polyelectrolyte–Cation Complexes Using PAsp-Ca&Mg Complexes

Dong-Ni Shen,Yue-Dan Xu,Cheng He,Zi-Huai Zhou,Hai-Hua Zhu,Ying Shi,Meng-Fei Yu,Jian Hu,Bai-Ping Fu

Magnesium ions are highly enriched in early stage of biological mineralization of hard tissues. Paradoxically, hydroxyapatite (HAp) crystallization is inhibited significantly by high concentration of magnesium ions. The mechanism to regulate magnesium-doped biomimetic mineralization of collagen fibrils has never been fully elucidated. Herein, it is revealed that citrate can bioinspire the magnesium-stabilized mineral precursors to generate magnesium-doped biomimetic mineralization as follows: Citrate can enhance the electronegativity of collagen fibrils by its absorption to fibrils via hydrogen bonds. Afterward, electronegative collagen fibrils can attract highly concentrated electropositive polyaspartic acid-Ca&Mg (PAsp-Ca&Mg) complexes followed by phosphate solution via strong electrostatic attraction. Meanwhile, citrate adsorbed in/on fibrils can eliminate mineralization inhibitory effects of magnesium ions by breaking hydration layer surrounding magnesium ions and thus reduce dehydration energy barrier for rapid fulfillment of biomimetic mineralization. The remineralized demineralized dentin with magnesium-doped HAp possesses antibacterial ability, and the mineralization mediums possess excellent biocompatibility via cytotoxicity and oral mucosa irritation tests. This strategy shall shed light on cationic ions-doped biomimetic mineralization with antibacterial ability via modifying collagen fibrils and eliminating mineralization inhibitory effects of some cationic ions, as well as can excite attention to the neglected multiple regulations of small biomolecules, such as citrate, during biomineralization process.

CAS / MDL: 7758-11-4 6132-04-3
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JOURNAL OF MATERIALS SCIENCE · 2016 ·Vol. 51 ·期 17 ·8139-8147 · IF 2.302

ZrC formation and the phase relations in the Si–Zr–Mg–O–C system

Sun W. Z.,Cheng J. G.,Huang Z. K.,Jiang Y.,Wu L. E.,Liu L. M.

When MgO+ZrO 2 were used as a sintering aid to SiC ceramics, it was found that ZrO 2 reacted with SiC and MgO to form ZrC and a magnesium silicate. This reaction may provide a new route to synthesize ZrC or prepare ZrC/SiC composites by reaction sintering using ZrO 2 , SiC, and MgO as starting materials. In the present work, formation process of the ZrC phase in the SiC–MgO–ZrO 2 system was addressed. Subsolidus phase relations at 1550 °C of the SiC–MgO–ZrO 2 system and the related SiC–SiO 2 –ZrC–ZrO 2 –MgO (Si–Zr–Mg–O–C) system were investigated.

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