INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
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2019
·
IF 3.375
Ting Li,Shuai Ma,Hu Yang,Zhen-liang Xu
Metal organic frameworks (MOFs) containing salt impurity provide a new idea for carbon material design. Presently, Mg–MOF/MgCl2 hybrid polycrystallines with different morphologies are solvothermally synthesized using 1,3,5-benzenetricarboxylic acid (BTC) or 1,4-benzenedicarboxylic acid (BDC) as the ligand, with or without polyethylene terephthalate (PET) inducer, respectively. After calcination, the products look like a flower, bud, cube, or nanosheet. When tested as adsorbent, the maximum methyl orange adsorption capacity reaches 3250 mg/g, the highest reported to date. The reason is attributed to the carbon-covered Mg salt inside the carbonized MOF. When tested as supercapacitor, carbonized MOFs based on BTC ligand show a high specific capacitance (127F/g) but a low rate capability, whereas a lower specific capacitance (121F/g) but a better rate capability (80% retention at 10A/g) are found for carbonized MOFs based on BDC. The reason is due to their different pore structures.
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高影响因子
HYDROMETALLURGY
·
2019
·
IF 3.465
Shuainan Ni,Caibin Wu,Yanliang Wang,Xiangguang Guo,Zeyuan Zhao,Xiaoqi Sun
Softening ammonia sulfate wastewater is one of the vital issues in the rare earth industry. In this article, a novel softening process using [4,4′-isopropylidenebis (phenoxyacetate)] (H 2 IPOAA) for Ca 2+ and Mg 2+ (M 2+ ) is developed. The effect factors, i.e., equilibrium time, pH value of aqueous phase and saponification degree are investigated. The extraction mechanism is proposed to be cation exchange. With a saponification degree of 85%, H 2 IPOAA is successfully used for the precipitation of Ca 2+ and Mg 2+ from ammonia sulfate wastewater within 10 min. The process can form precipitated particles with an average size of 35 μm, which are much larger than the precipitates formed by H 2 C 2 O 4 , Na 2 C 2 O 4 and Na 2 CO 3 . The precipitated particles can be easily separated from the raffinate. In addition, H 2 IPOAA is repeatedly used for five times with a little loss. To a considerable extent, the reuse of H 2 IPOAA contributes to lowering the cost and reducing the pollution. The concentrations of Ca 2+ and Mg 2+ in the raffinate extracted by H 2 IPOAA are up to the MVR standard for wastewater treatment . The economical and efficient softening process meets the need of green chemistry, which is expected to replace traditional industrial processes for water softening based on H 2 C 2 O 4 , Na 2 C 2 O 4 and Na 2 CO 3 .
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JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY
·
2018
·Vol. 94
·期 1
·167-177
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IF 2.587
Xuejuan Cao,Junnan Wei,Huai Liu,Xinyue Lv,Xing Tang,Xianhai Zeng,Yong Sun,Tingzhou Lei,Shijie Liu,Lu Lin
BACKGROUND γ-Valerolactone (GVL) is a versatile biomass-derived platform molecule that could serve as a building block to produce chemicals, materials and fuels, but the production of GVL from biomass via a cost-competitive method is challenging. In this contribution, a robust Cu─Mg oxide was prepared as an efficient bifunctional catalyst for both H 2 production by MeOH reforming and hydrogenation of methyl levulinate (ML) to GVL in MeOH medium. RESULTS Cu 0.87 Mg 0.13 O x prepared by a urea hydrolysis method offered a GVL yield up to 90.6% at 220°C in 4 h without external hydrogen. This catalyst could be reused for at least seven consecutive cycles without loss of its activity. Notably, Cu 0.87 Mg 0.13 O x also provided nearly 70% GVL yield in methanolysis products of cellulose in the presence of humins. Characterization of the catalyst indicates that the incorporation of MgO greatly facilitates the stabilization of Cu + species that possess a better catalytic performance in ML hydrogenation compared with metallic Cu. CONCLUSION This robust Cu 0.87 Mg 0.13 O x could greatly contribute to develop a highly facile and desirable two-step strategy for GVL production from cellulose, through the integration of ML production by methanolysis of cellulose, H 2 formation by MeOH reforming and ML hydrogenation in MeOH medium. © 2018 Society of Chemical Industry
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Materials
·
2018
·Vol. 11
·期 7
·1113
·
IF 2.467
Zhe Wang,Xiaoping Shen,Temeng Qian,Kang Xu,Qingfeng Sun,Chunde Jin
The hydrophilicity and flammability of fiberboards have limited their real-life applications. In this study, a facile strategy for preparing the multifunctional coatings with superhydrophobicity and flame retardancy on medium density fiberboards (MDFs) has been investigated. The superhydrophobic and flame-retardant coating on the MDF surface was obtained by depositing polydimethylsiloxane (PDMS) and 1H, 1H, 2H, 2H-perfluorodecyltrichlorosilane (FDTS)-modified Mg/Al layered double hydroxide (LDH) particles step by step. The as-prepared coating exhibited superhydrophobic properties with a water contact angle (WCA) of ~155° and good self-cleaning properties. Furthermore, the limiting oxygen index (LOI) value of the superhydrophobic MDFs increased by 60.4% as compared to that of the pristine MDFs, showing improved flame retardancy. The peak heat release rate (PHRR) and total heat release (THR) of MDFs decreased after coating with PDMS@FDTS-Mg/Al LDH, suggesting that the superhydrophobic coating decreased the fire growth speed and risk of fire hazard of MDFs. This coating with multiple functions opens a new avenue for the protection and functionalization of MDFs.Keywords:medium density fiberboard;Mg/Al LDH;FDTS;superhydrophobicity;flame retardancy
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PubMed
高影响因子
Journal of Physical Chemistry C
·
2013
·
IF 4.814
Yongfeng Liu,Chao Li,Bo Li,Mingxia Gao,Hongge Pan
The hydrogen storage properties and mechanisms of the Mg(NH2)2–2LiH system with potassium halides (KF, KCl, KBr, and KI) were investigated and discussed. The results show that the KF-added sample exhibits superior hydrogen storage properties as ∼5.0 wt % of hydrogen can be reversibly stored in the 0.08KF-added sample via a two-stage reaction with an onset dehydrogenation temperature of 80 °C. However, hydrogen storage behaviors of the samples with KCl, KBr, and KI remain almost unchanged. The fact that KF can readily react with LiH to convert to KH and LiF due to the favorable thermodynamics during ball milling should be the primary reason for its significant effects, as the presence of KH provides a synergetic thermodynamic and kinetic destabilization in the hydrogen storage reaction of the Mg(NH2)2–2LiH system by declining the activation energy of the first-step dehydrogenation as a catalyst and reducing the desorption enthalpy change of the second step as a reactant. The understanding on the role played by KF sheds light on how to further decrease the operating temperature and enhance the hydrogen storage kinetics of the metal–N–H system.
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RSC Advances
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2014
·Vol. 4
·期 81
·42764-42771
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IF 3.708
Yana Liu,Jinxin Zou,Xiaoqin Zeng,Wenjiang Ding
A Mg–Ti nano-composite has been co-precipitated from a tetrahydrofuran (THF) solution containing anhydrous magnesium chloride (MgCl2), titanium tetrachloride (TiCl4) and lithium naphthalide (LiNp) as the reducing agent. X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning transmission electron microscopy (STEM), and pressure-composition-temperature (PCT) techniques are used to characterize phase components, microstructure and hydrogen sorption properties of the composite. The co-precipitated Mg–Ti nano-composite contains nearly 1.0 wt% of Ti distributed homogeneously on the surface or inside Mg particles having an average particle size of about 50 nm. Orthorhombic γ-MgH2 phases and tetragonal γ-TiH2 phases are obtained when the Mg–Ti nano-composite is hydrogenated at 75 °C. PCT measurements reveal the superior hydrogen absorption property of the Mg–Ti nano-composite: its maximum hydrogen capacity can reach up to 6.2 wt% within 2 h at room temperature under a hydrogen pressure of 3 MPa. The activation energy for hydrogen absorption is determined to be 50.2 kJ mol−1 H2. The hydrogenation and dehydrogenation enthalpies of the nano-composite are calculated to be −73.0 ± 1.8 and 75.8 ± 4.7 kJ mol−1 H2, close to the standard values for Mg (−74.1 ± 2.9 kJ mol−1 H2). The catalytic effects from the co-precipitated Ti and the tetragonal γ-TiH2 formed during the hydrogenation process lead to extremely fast absorption kinetics at room temperature.
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高影响因子
MATERIALS LETTERS
·
2015
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IF 2.489
Xiwei Liu,Jianke Sun,Yinghong Yang,Feiyu Zhou,Zhongjie Pu,Li Li,Yufeng Zheng
The microstructure, mechanical properties , in vitro degradation behavior and hemocompatibility of novel Zn–1Mg–0.1Sr and Zn–1Mg–0.5Sr (wt%) ternary alloys were evaluated with pure Zn as control. The results indicated that Zn–Mg–Sr alloys exhibited much higher yield strength (YS), ultimate tensile strength (UTS), hardness and corrosion rate than those of pure Zn. But their elongation and hemolysis rates were reduced. Furthermore, the hot-rolled Zn–1Mg–0.1Sr alloy presented the superior mechanics performance (196.84±13.20 MPa, 300.08±6.09 MPa, 22.49±2.52%, 104.31±10.18 for YS, UTS, Elongation and hardness, respectively), appropriate corrosion rate (0.15±0.05 mm/year) and excellent hemocompatibility (hematolysis rate of 1.10±0.2% and no signs of thrombogenicity), showing a preferable candidate as the biodegradable implant material .
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JOURNAL OF ALLOYS AND COMPOUNDS
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2017
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IF 3.133
Li-Feng Zhu,Bo-Ping Zhang,Shun Li,Gao-Lei Zhao
The (1- x )Bi 1+ y (Fe 0.96 Mg 0.02 Ti 0.02 )O 3 - x BaTiO 3 (abbreviated as B 1+ y FMT- x BT) system was designed to explore the morphotropic phase boundary (MPB) separating rhombohedral ( R ) and tetragonal ( T ) phases, and the mechanism of performance enhancement. The phase structure of samples was discreetly investigated by X-ray diffraction, and Rietveld refinement results of the XRD data revealed that the B 1+ y FMT- x BT ceramics consist of an R phase at x = 0.24, two R and T phases at 0.26 ≤ x ≤ 0.32, and a single T phase at x = 0.34. Because of the MPB and the improvement of resistivity with adding excess Bi compensation, excellent piezoelectric properties of d 33 = 198 pC/N and k p = 30.9%, as well as high Curie temperature T C = 497 °C were achieved in the B 1+ y FMT- x BT system at x = 0.30 and y = 0.02. Here, the large d 33 = 198 pC/N which is the maximum value for the BF-BT-Bi(Mg,Ti)O 3 system so far, and high T C = 497 °C suggest that Bi(Fe,Mg,Ti)O 3 -BaTiO 3 ceramics have good prospects in high-temperature piezoelectric devices.
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JOURNAL OF WUHAN UNIVERSITY OF TECHNOLOGY-MATERIALS SCIENCE EDITION
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2016
·Vol. 31
·期 6
·1211-1218
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IF 0.4
Zhang Dan,Zhao Guoqing,Yu Jingang,Yan Tao,Zhu Mingyue,Jiao Feipeng
Adsorption of 2, 4, 6-trichlorophenol (TCP) onto the calcined Mg/Al-CO 3 layered double hydroxide (CLDH) was investigated. The prepared Mg/Al-CO 3 layered double hydroxide (LDH) and CLDH were characterized by powder X-ray diffraction (XRD) and thermo gravimetric analyzer-differential scanning calorimeters (TG-DSC). Moreover, 2,4,6-trichlorophenol (TCP) was removed effectively (94.7% of removal percentage in 9 h) under the optimized experimental conditions. The adsorption kinetics data fitted the pseudo-second-order model well. The Freundlich, Langmuir, and Tempkin adsorption models were applied to the experimental equilibrium adsorption data at different temperatures of solution. The adsorption data fitted the Freundlieh adsorption isotherm with good values of the correlation coefficient. A mechanism of the adsorption process is proposed according to the intraparticle diffusion model, which indicates that the overall rate of adsorption can be described as three steps.
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CHEMICAL ENGINEERING JOURNAL
·
2017
·
IF 6.216
Xin Huang,Man Su,Jizhi Zhou,Weikang Shu,Zhifeng Huang,Naiyun Gao,Guangren Qian
Persulfate based advanced oxidation processes have been well investigated, with the generation of radical species via various activation methods. This study reports an activation pathway of peroxydisulfate (S 2 O 8 2− , PDS) without radical production, achieved by the intercalation of PDS into Mg/Al-layered double hydroxide (LDH). Physical characterization indicated that the LDH was intercalated by PDS with the interlayer distance increasing to 0.917 nm. Approximately 93.9% of the phenol was decomposed by a LDH-PDS composite containing 0.4 mmol/g PDS, whilst no removal of phenol was achieved in the control group with PDS. Moreover, sulfate from decay of PDS was likely kept in the layers of LDH for no sulfate leakage in solution was observed. This is in accordance with the occurrence of characteristic peaks assigned for sulfate in FT-IR spectrum of LDH-PDS after reaction. Interestingly, radicals were not recorded by electron spin resonance measurement or radical scavenger tests during the oxidation process. The reactivity of PDS was likely improved by the basic sites on the LDH laminate, which provided OH to activate the O O bond in PDS. Further, the limited space of LDH layers reduce the bond cleavage of intercalated PDS and thus the generation of radicals. Therefore, the results proposed a non-radical reaction between phenol and PDS in the interlayer of LDH and developed a novel activation pathway for PDS in the elimination of organic contaminants.
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APPLIED THERMAL ENGINEERING
·
2024
·
IF 6.1
Lisheng Deng,Shusen lin,Linfa Xiao,Mitsuhiro Kubota,Hongyu Huang,Jun Li,Dezhen Chen
The application of MgO/Mg(OH) 2 in heat storage technology has been limited due to slow hydration rate and easy agglomeration. In this paper, nanoporous carbon particle (NCP) as a carrier was used to prepare NCP/MgO chemical heat storage composite materials by impregnation and calcination methods, respectively. The microstructure characterization, hydration reaction, and simultaneous thermogravimetric analysis experiments were carried out on the prepared composite materials. The results showed that the internal distribution of MgO in the composite material prepared by calcination method was more uniform, and the particle size of MgO was smaller. Under the conditions of 110 ℃ hydration temperature and 57.8 kPa water vapor partial pressure, the hydration conversion ratio of the composite material prepared by calcination method after 120 min of hydration conversion ratio reached 93 %, which was 17.7 % higher than that of the impregnated composite material and 50 % higher than that of pure MgO. Under the comprehensive influence of specific surface area, pore structure, and active component particle size, compared with pure materials and impregnated composite materials, the dehydration rate of the composite material prepared by calcination method at 300 ℃ was twice that of impregnated method and 6 times that of pure MgO, and the heat storage density reached 1039kJ/kg. After 10 cycles, the heat storage density still maintained an initial state of 95.8 %. Compared with pure materials and impregnated composite materials, NCP/MgO composite materials prepared by calcination method had better heat storage performance and higher cyclic stability.
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FATIGUE & FRACTURE OF ENGINEERING MATERIALS & STRUCTURES
·
2024
·Vol. 47
·期 8
·2905-2921
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IF 3.1
Siran Wang,Zhangcheng Yin,Xudong Rong,Haipeng Song,Xudong Yang,Naiqin Zhao
The unsatisfactory fatigue performance of Al foams significantly limits their engineering applications. Meanwhile, the unique pore structure of metal foams makes it still challenging to assess its fatigue. Herein, we report an innovative strategy for preparing carbon nanotubes reinforced Al-Cu-Mg (CNTs/Al-Cu-Mg) composite foams, which exhibit superior compressive strength (16.17 MPa) and fatigue strength (11.17 MPa). Statistics analysis confirms that the fatigue life ( N f ) follows Weibull distribution, and P-S-N curves were obtained to calculate the theoretical stress level required to achieve the expected N f . Moreover, computer vision is utilized to monitor the fatigue deformation process and effectively detect fatigue crack initiation sites. Notably, the accuracy of predicted N f obtained by this method is exceptionally high (98.32%). This work provides a theoretical and practical basis for designing metal foams with superior fatigue properties and offers a promising bottom-up tactic for predicting the N f of metal foams to prevent fatigue failure. Highlights The CNTs/Al-Cu-Mg composite foams possess the superior fatigue strength of 11.17 MPa. The application of computer vision enables the accurate monitoring of FCIS. A novel exploration into the fatigue assessment of metal foams is developed.
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危险品化学品经营许可证（带存储）