CHEMICAL ENGINEERING JOURNAL
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2021
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IF 13.273
Rui Ma,Xueqian Yan,Xiaohui Mi,Yaoguo Wu,Jin Qian,Qiuyu Zhang,Guang-Hao Chen
In this study, the Mg-Fe-LDH@biochar composite was firstly fabricated and applied for effectively activation peroxymonosulfate (PMS) for aqueous doxycycline (DOX) degradation. The physiochemical properties of the as-synthesized composite were thoroughly characterized. In the developed Mg-Fe-LDH@biochar/PMS system, the catalytic DOX degradations were evaluated under different conditions. Under the optimal condition (0.75 g/L catalyst loading, 0.75 g/L PMS dosage, pH = 7.0), about 88.76% DOX (35 mg/L) was removed within 120 mins. The results of quenching test and electron paramagnetic resonance (EPR) illustrated that the •OH, SO 4 • - and •O 2 – radicals all contributed to the DOX degradation in the Mg-Fe-LDH@biochar/PMS system, whereas the 1 O 2 -based non-radical degradation played the dominant role in DOX removal. The developed system was almost not adversely affected by the high-strength anions and exhibited high DOX decomposition rates in a wide pH range from 3.0 to 9.0, indicating the great potential in the practical application. The satisfactory reusability of the composite catalyst was demonstrated in the recycling test, with the DOX removal efficiency slightly declined from 90.08 to 84.42% after five runs. Based on the generation of reactive oxidative species and the transformation intermediates identified by HPLC-MS, the possible degradation pathways and reaction mechanism of DOX degradation in Mg-Fe-LDH@biochar/PMS system were proposed.
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CHEMICAL ENGINEERING JOURNAL
·
2019
·
IF 8.355
Lingchao Kong,Yu Tian,Zheng Pang,Xiaohong Huang,Ming Li,Ning Li,Jun Zhang,Wei Zuo,Junjing Li
Phosphate and fluoride are primary culprits of water eutrophication and skeleton fluorosis, respectively, severely threatening the security of aquatic lives and public health. To deal with the aqueous phosphate and fluoride pollution, PC@La nanocomposites were tailor-designed based on low-cost periclase and lanthanum salt via a facile urea hydrothermal method. Results from SEM, XRD, FTIR, XPS analysis revealed the PC@La-1.0 was constructed by Mg-La bimetal carbonated hydroxides with the three-dimensional needle-like nanostructure. Highly effective adsorption capacities for both phosphate (107.34 mg/g) and fluoride (63.11 mg/g) were achieved by PC@La-1.0. The adsorption was pH-dependent, and the optimal pH values for adsorption was 4.0–6.0. Over 80% of initial adsorption capacities remained after four adsorption–desorption cycles, indicating its satisfactory reusability. Superior adsorption selectivity for phosphate and fluoride was proven when co-existing with common ions and organics in solutions and real sewage. Mechanism analysis revealed that the unique structure of Mg-La bimetal carbonate hydroxide structure of PC@La-1.0 promoted an accumulative anion adsorption performance. Mg and La cations on PC@La-1.0 formed strong inner-sphere complexation with target phosphate and fluoride while the internal carbonate and hydroxyl groups contributed to adsorption via ion exchange. This study highlights the novel low-cost method to prepare promising candidates for efficient dephosphorization and defluorination from water.
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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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JOURNAL OF MATERIALS RESEARCH
·
2015
·Vol. 30
·期 10
·1639-1647
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IF 1.647
Xueming Liu,Chunge Niu,Xinping Zhen,Jide Wang,Xintai Su
A phase transfer method was developed to prepare Mg(OH)2 nanosheets and a subsequent adsorption–calcination process was followed to obtain lamellar MgO nanostructures. The as-prepared MgO nanosheets also showed a superior adsorption property of Congo red. Transmission electron microscopy and x-ray diffractometer results indicated that the as-obtained Mg(OH)2 was plate-shaped with a hexagonal crystal structure where MgO possessed a lamellar structure with a cubic phase. The maximum adsorption capacities of Mg(OH)2 and MgO were reached up to 1820 and 2650 mg g−1, respectively. The high adsorption capacity might be related to the particle geometry and large surface area (87.97 m2 g−1 for Mg(OH)2 and 132.31 m2 g−1 for MgO). The adsorbents can be easily regenerated for five times without any significant loss in their adsorption property. The adsorption behaviors of the Mg(OH)2 and MgO adsorbents showed that the adsorption kinetics and isotherms were in good agreement with pseudo-second-order rate equation and Freundlich adsorption model.
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高影响因子
ACS Applied Materials & Interfaces
·
2016
·
IF 7.145
Jing Liu,Bo Zheng,Pei Wang,Xingang Wang,Bin Zhang,Qiuping Shi,Tingfei Xi,Ming Chen,Shaokang Guan
Bioabsorbable magnesium alloys are becoming prominent as temporary functional implants, as they avoid the risks generated by permanent metallic implants such as persistent inflammation and late restenosis. Nevertheless, the overfast corrosion of Mg alloys under physiological conditions hinders their wider application as medical implant materials. Here we investigate a simple one-step process to introduce a cross-linked 3-amino-propyltrimethoxysilane (APTES) silane physical barrier layer on the surface of Mg–Zn–Y–Nd alloys prior to electrostatic spraying with rapamycin-eluting poly(lactic-co-glycolic acid) (PLGA) layer. Surface microstructure was characterized by scanning electron microscope and Fourier transform infrared spectroscopy. Nanoscratch test verified the superior adhesion strength of PLGA coating in the group pretreated with APTES. Electrochemical tests combined with long-term immersion results suggested that the preferable in vitro anticorrosion behavior could be achieved by dense APTES barrier. Cell morphology and proliferation data demonstrated that APTES pretreated group resulted in remarkably preferable compatibility for both human umbilical vein endothelial cells and vascular smooth muscle cells. On the basis of excellent in vitro mechenical property, the animal study on the APTES pretreated Mg–Zn–Y–Nd stent implanted into porcine coronary arteries confirmed benign tissue compatibility as well as re-endothelialization without thrombogenesis or in-stent restenosis at six-month followup.
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PubMed
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2024
·
IF 8.1
Yu Yang,Meng Du,Jiaxin Liang,Qian Xu,Wei Liu,Ang Li
The flow-through electroactive membrane adsorption method has been proved to be a promising strategy to enrich low-concentration phosphate. However, the challenges of selective adsorption of phosphate and poor regeneration restrict its industrial application. Here, this study proposed a novel bimetallic Mg-UiO-66@rGO electrode material through the introduction of Mg(II) into UiO-66, which possessed remarkable adsorption selectivity and optimal reproducibility among the reported electrode materials. The maximum phosphate adsorption capacity of Mg-UiO-66(13)@rGO (Zr/Mg = 3:1) was 62.81 mg⋅g −1 at 3.2 V. Furthermore, it maintained the excellent adsorption properties in the presence of all competitive anions and after 30 times of continuous adsorption–desorption. In actual wastewater, Mg-UiO-66(13)@rGO still represented excellent adsorption kinetics of 0.51 mg⋅(g⋅min) −1 and equilibrium adsorption capacity of 61.2 mg⋅g −1 . The superior selectivity of Mg-UiO-66@rGO was attributed to the establishment of coordinative unsaturated metal sites (CUMSs), thus increasing the adsorption sites. The synergic effect of electric field facilitates the breaking and formation of coordination bonds between charged ions and deeper binding sites, boosting the adsorption–desorption ability. Notably, the structural stability is also a key factor in promoting repeated material regeneration. This study advances electrode material to a new level by introducing CUMSs and bimetallic synergies.
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SEMICONDUCTOR SCIENCE AND TECHNOLOGY
·
2025
·Vol. 40
·期 3
·035006
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IF 2.1
Xingyu Zhang,Lingling Wang,Yawei Wang,Xiangyang Zhao,Rong Fang,Rui Guo,Yue Zhou,Xintong Zhang,Yichun Liu
Modifying the back contact interface plays a key role in improving the efficiency of Cu2ZnSn(S,Se)4 (CZTSSe) solar cells. Aiming at the phase decomposition and carrier recombination issues in the CZTSSe/Mo back contact interface, an ultra-thin Mg(OH)2 intermediate layer was introduced between the Mo substrate and the CZTSSe absorber layer. The Mg(OH)2 intermediate layer effectively suppressed the interface phase decomposition reactions and inhibited the generation of interface secondary phases. Meanwhile, during the high-temperature selenization process, the Mg2+ doped into CZTSSe at the back contact interface, reducing the defects and band offset at the CZTSSe/Mo interface. The performance of the device was improved, with a significant increase in efficiency compared to the control device. This work highlights the modification effect of Mg(OH)2 for improving back contact and also provides an easy-handling method to achieve high-performance CZTSSe solar cells.
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CERAMICS INTERNATIONAL
·
2024
·
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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CHEMOSPHERE
·
2024
·
IF 8.1
Yingchao Li,Shujia Wang,Xiao Fang Ouyang,Zhi Dang,Hua Yin
The simultaneous removal of anionic and cationic heavy metals presents a challenge for adsorbents. In this study, acetate (Ac-) was utilized as the intercalating anion for layered double hydroxide (LDH) to prepare a novel biochar composite adsorbent (Ac-LB) designed for the adsorption of Pb(II), Cu(II), and As(V). By utilizing Ac- as the intercalating anion, the interlayer space of the LDH was enlarged from 0.803 nm to 0.869 nm, exposing more adsorption sites for the LDH and enhancing the affinity for heavy metals. The results of the adsorption experiments showed that the adsorption effect of Ac-LB on heavy metals was significantly improved compared to the original FeMg-LDH modified biochar composites (LB), and the maximum adsorption capacity of Pb(II), Cu(II), and As(V) were 402.70, 68.50, and 21.68 mg/g, respectively. Wastewater simulation tests further confirmed the promising application of Ac-LB for heavy metal adsorption. The analysis of the adsorption mechanism revealed that surface complexation, electrostatic adsorption, and chemical deposition were the main mechanisms of action between heavy metals (Pb(II) and Cu(II)) and Ac-LB. Additionally, Cu(II) ions underwent a homogeneous substitution reaction with Ac-LB. The adsorption process of As(V) by Ac-LB mainly relied on complexation and ion-exchange reactions. Lastly, the modification of the LDH structure by Ac − as an intercalating anion, thereby increasing the affinity for heavy metals, was further illustrated using density-functional theory (DFT) calculations.
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PubMed
高影响因子
POLYMER
·
2024
·
IF 4.1
Xiaoyu Luo,Xiangjun Li,Miaomiao Li,Donghai Ding,Libo Tong
Two-dimensional (2D) nanocomposite coatings and superhydrophobic coatings are applied to retarding corrosion of Magnesium (Mg) and its alloys. However, stability of the delicate micro/nanostructure and corrosion durability are still intractable issues. In this work, a bi-layer superhydrophobic coating with excellent corrosion resistance has been successfully constructed on Mg alloy via a facile spray/spin assisted self-assembly technique. The polyurethane (PU) coating containing well-dispersed hydroxylated hexagonal boron nitride (OH-BN) nanoparticles acts as the barrier layer and “adhesive”, while the superhydrophobic modified h-BN (f-BN) nanoparticles serve as the water-repellent surface. In addition, the modifying agents containing dynamic disulfide bonds provide covalent bonding effect to construct a stable superhydrophobic surface. Hence, the obtained coating presents extreme non-wettability with an impressive static water contact angle (WCA) of 155° as well as possesses outstanding anti-water adhesion, anti-fouling and self-cleaning performance. Meanwhile, the designed coating shows excellent corrosion durability, which the value of |Z| f = 0.01 Hz retains at 9.5 × 10 9 Ω cm 2 , higher than PU coating of two orders of magnitude. The developed coating shows promising potentials as a durable protective material for Mg alloy and other metals and alloys, shedding new lights on developing high-performance corrosion resistance technologies.
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SURFACE & COATINGS TECHNOLOGY
·
2025
·
IF 6.1
Wenyi Qiu,Xinglong Ye,Yan Liu,Bin Lin,Junfeng Chen,Lei Xiao,Chen Wang,Bingshu Wang,Xiping Cui,Linchi Zou
In order to achieve in-situ growth of layered double hydroxides (LDH) film on plasma electrolytic oxidation (PEO) coating of AZ31B magnesium alloy under mild conditions, a facile method was used in this work, that is ethylenediaminetetraacetic acid (EDTA)-assisted growth method. Compared to the conventional hydrothermal method, the fabrication of LDH/PEO composite coating by this method does not require a high temperature and high pressure environment and is not constrained by the size of the reactor. Furthermore, the obtained LDH/PEO composite coating exhibits enhanced corrosion protection, which will be widely applied in corrosion protection field of surface engineering. In this work, an effective strategy to control the dissolution of PEO coating and the growth of LDH film by regulating the concentration of EDTA was proposed, after revealing the growth behavior of LDH on PEO coating during this facile fabrication process. The growth behavior of LDH film can be briefly summarized in three stages: PEO coating dissolution, LDH nucleation, and LDH growth. Interestingly, the growth mechanism of LDH was changed with EDTA assistance. LDH shifted from preferential growth within the micropores of the PEO coating to uniform growth. With the assistance of 0.06 M EDTA, which is optimal, the dissolution of original PEO coating provided a stable and sufficient Mg source for the growth of LDH film, resulting in a dense LDH network structure on the PEO coating. This uniformly grown LDH film could not only seal the inherent defects of the PEO coating but also exhibited the ability to adsorb corrosive anions, which increases the tortuosity and difficulty in penetration of corrosive media, significantly improving the corrosion resistance of the LDH/PEO composite coating.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2024
·
IF 5.8
Wen Wang,Chuyuan Lin,Fenqiang Luo,Renpin Liu,Xiaochuan Chen,Wangyang Wu,Shiting Wei,Fuyu Xiao,Peixun Xiong,Qinghua Chen,Qingrong Qian,Lingxing Zeng
Hybrid magnesium-lithium batteries (MLIBs) are a promising battery system with safety and exceptional reaction kinetics due to the combination of the dendritic-free deposition Mg metal anode and the rapid Li intercalation cathode. The large interchain frame of VO 2 may contribute to the metal-ion diffusion, making it a suitable cathode for MLIBs. However, the development of VO 2 cathodes for MLIBs is restricted by bad structural stability and low electronic conductivity. Herein, MoS 2 with a hexagonal crystal structure is introduced into the tetragonal VO 2 to construct heterostructure interfaces and induce abundant oxygen vacancies (VO 2 /MoS 2 -2), which enhances the structural stability and reaction kinetics. For this reason, the VO 2 /MoS 2 -2 cathode delivers a remarkable capacity (518 mAh g -1 ) and a considerable cycling lifespan (202 mAh g -1 at 1.0 A g -1 over 700 cycles). Even at low temperatures (-15 and -40 °C), VO 2 /MoS 2 -2 delivers 145 and 115 mAh g -1 after 200 and 50 cycles at 0.1 A g -1 , respectively. This strategy of combinatorial design offers a widely applicable method for the cryogenic resistance and cycling durability of magnesium-lithium batteries.
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