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ANALYTICAL CHEMISTRY · 2013 · IF 5.695

Fluorescent Metal–Organic Framework MIL-53(Al) for Highly Selective and Sensitive Detection of Fe3+ in Aqueous Solution

Cheng-Xiong Yang,Hu-Bo Ren,Xiu-Ping Yan

Fluorescent metal–organic frameworks (MOFs) have received great attention in sensing application. Here, we report the exploration of fluorescent MIL-53(Al) for highly selective and sensitive detection of Fe3+ in aqueous solution. The cation exchange between Fe3+ and the framework metal ion Al3+ in MIL-53(Al) led to the quenching of the fluorescence of MIL-53(Al) due to the transformation of strong-fluorescent MIL-53(Al) to weak-fluorescent MIL-53(Fe), allowing highly selective and sensitive detection of Fe3+ in aqueous solution with a linear range of 3–200 μM and a detection limit of 0.9 μM. No interferences from 0.8 M Na+; 0.35 M K+; 11 mM Cu2+; 10 mM Ni2+; 6 mM Ca2+, Pb2+, and Al3+; 5.5 mM Mn2+; 5 mM Co2+ and Cr3+; 4 mM Hg2+, Cd2+, Zn2+, and Mg2+; 3 mM Fe2+; 0.8 M Cl–; 60 mM NO2– and NO3–; 10 mM HPO42–, H2PO4–, SO32–, SO42–, and HCOO–; 8 mM CO32–, HCO3–, and C2O42–; and 5 mM CH3COO– were found for the detection of 150 μM Fe3+. The possible mechanism for the quenching effect of Fe3+ on the fluorescence of MIL-53(Al) was elucidated by inductively coupled plasma-mass spectrometry, X-ray diffraction spectrometry, and Fourier transform infrared spectrometry. The specific cation exchange behavior between Fe3+ and the framework Al3+ along with the excellent stability of MIL-53(Al) allows highly selective and sensitive detection of Fe3+ in aqueous solution. The developed method was applied to the determination of Fe3+ in human urine samples with the quantitative spike recoveries from 98.2% to 106.2%.

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RSC Advances · 2014 ·Vol. 4 ·期 64 ·34008-34013 · IF 3.708

Effect of sintering temperature on the phase structure and electrical properties of Al–N co-doped BaTiO3 piezoceramics

Dan Xu,Weili Li,Lidong Wang,Wei Wang,Wei-Dong Fei

BaTiO3 and 1.5 mol% AlN/BaTiO3 (AlN/BT) piezoceramics were prepared via a conventional solid-state reaction method. The effects of sintering temperature on the phase structure, preferential orientation degree of Al3+–N3− pairs and electrical properties of the ceramics were investigated and analyzed. The AlN/BT ceramic sintered at 1325 °C obtains the optimum piezoelectric properties of d33 = 305 pC N−1, kp = 0.33 and Qm = 140 due to the preferential distribution of Al3+–N3− pairs and suitable sintering temperature. The high temperature stability testing reveals that these AlN-doped BT ceramics are useable at temperatures as high as approximately 115 °C. These properties indicate that this system is a potential high piezoelectric lead-free candidate material to be further studied.

CAS / MDL: 95-16-9
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Analytical Methods · 2015 ·Vol. 8 ·期 1 ·214-221 · IF 1.821

Near infrared fluorescence-magnetic resonance dual-modal imaging with Cy5-labeled, Gd–Al co-doped mesoporous silica nanoparticles

Ai Gao,Dan Zhang,Xue-Bo Yin

To obtain comprehensive information and to compensate the limits of individual modalities in molecular imaging, the research on dual-modal imaging probes (DMIPs) attracts much interest. Here, we report a reliable and facile procedure to prepare near infrared fluorescence (NIRF)-magnetic resonance (MR) DMIPs using Cy5-labeled, Gd–Al co-doped mesoporous silica nanoparticles (MSNs). Amine-modified, Gd–Al co-doped MSNs were first synthesized through one-step co-condensation. A Cy5-NHS ester was then coupled to the amino groups to produce the DMIPs, which were denoted as Gd–Al@MSNs-Cy5. High intensity NIRF and a relaxation rate (17.7 mM−1 s−1) were observed. Featuring the lower background and the deeper penetration depth, the cutting-edge NIRF imaging was achieved. Moreover, the larger surface area of MSNs could be modified with more NIRF probes, Cy5, for improved NIRF. Following the Solomon–Bloembergen–Morgan theory, enhanced MR performance was illustrated by the relaxation rate because MSNs have a porous structure that enables access of water into the interior, and co-doping with Al in the MSNs promotes the doped amount of Gd. The exchange rate of water is much more accelerated through doping Gd and Al since a disordered pore arrangement is found in Gd–Al co-doped MSNs. The DMIPs in saline were injected into mice through the tail vein for imaging and basic pharmacokinetics studies. They were excreted by the stomach and intestine in 3 h, a circulation time long enough for imaging. Thus, Gd–Al@MSNs-Cy5 are attractive for clinical NIRF-MR dual-modal imaging by integrating the biocompatibility of MSNs, the NIRF of Cy5, and the high MR response of Gd.

CAS / MDL: 7446-70-0 12064-62-9
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THERMOCHIMICA ACTA · 2024 · IF 3.1

Effects of Cu(OH)F nanoparticles on the thermal oxidation and ignition characteristics of micron-sized Al powder

Jiaming Liu,Xinwen Ma,Wenhao Wang,Weiduo Fei,Xiandie Zhang,Xiang Ke,Xiang Zhou

In this study, Cu(OH)F nanoparticles are prepared through a simple hydrothermal reaction and their effects on the thermal oxidation and ignition characteristics of micron-sized Al powder (μ-Al) are explored for the first time. Thermal analysis in air atmosphere (50∼1050 °C) shows that compared to raw μ-Al, the normalized weight gain of Al in Al-Cu(OH)F increases by about 36.9%, 64.8%, and 106.3% when the added Cu(OH)F is 1 wt%, 3 wt%, and 5 wt%, respectively. After mixed with NH 4 ClO 4 , electric ignition and open-air combustion tests show shortened ignition delay time (by 42.6%∼63.8%) and increased maximum light intensity (by 48.9%∼117.8%) for Al-Cu(OH)F. The effects of Cu(OH)F result from its decomposition products, namely, HF and CuO. HF reacts with alumina shell to form AlF 3 , which sublimes at high temperature and thus exposes Al core instantly, while CuO can react with Al core to release heat, further facilitating the thermal oxidation and ignition processes.

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APPLIED SURFACE SCIENCE · 2024 · IF 6.3

Efficient preparation of core–shell Al@PFHP@fluoropolymer energetic composites combining corrosion resistance and high energy release properties

Xiandie Zhang,Linfeng Yue,Heng Xu,Haozhe Li,Jiaming Liu,Xiang Zhou,Xiaode Guo

The study employed a two-step synthesis method to prepare Al@PFHP@fluoropolymer energetic composites with a core–shell structure. PFHP and HF acid are used for surface etching and modification of raw Al powder. PFHP bonds to the surface of Al powder, with redundant C-F providing hydrogen bonding sites, driving dissolved PVDF and P(VDF-HFP) polymer chains in the liquid phase to migrate, nucleate, and grow on the surface of the Al powder, and consequently the formation of a continuous shell layer through hydrogen-bonding self-assembly. The Al powder coated with fluoropolymer exhibited strong hydrophobic and corrosion-resistant properties, ensuring long-term storage and environmental adaptability. Compared to mechanically mixed Al@PFHP/fluoropolymer, the Al@PFHP@fluoropolymer composites show significant improvements in thermal reactivity, ignition, and combustion performance. The close integration of fluoropolymer and Al shortens the mass and heat transfer distances during the reaction process. Additionally, the low-boiling-point AlF 3 does not hinder diffusion process in the combustion zone, which is conducive to the alleviation of the reaction sintering phenomenon and the rapid and concentrated release of energy. Therefore, through the dual strategy of using fluorine-containing oxidizers and structure optimization, efficient reaction of Al@PFHP@fluoropolymer is achieved, also promoting efficient combustion of Al powder. The synthesis process of this energetic composite is simple yet yields exceptionally high performance, enabling large-scale production and application potential in military ammunition and rocket propulsion systems.

CAS / MDL: 64-17-5 68-12-2 109-99-9
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TRANSACTIONS OF NONFERROUS METALS SOCIETY OF CHINA · 2024 · IF 4.7

Efficient removal of Al(III) and P507 from high concentration MgCl2 solution based on in-situ reaction strategy

Qiang WANG,Meng WANG,Zong-yu FENG,Yong-qi ZHANG,Xiao-wei HUANG,Xiang-xin XUE

For a highly efficient recycling of a wastewater containing a high concentration of MgCl 2 , Al(III) and P507 were scheduled to be removed in advance. In this study, the in-situ removal of Al(III) and P507 from a high concentration MgCl 2 solution at different pH values and Al/P molar ratios was investigated. The results showed that P507 formed organic complexes of Al x (OH) z + y -P507 at pH of 2.0−4.0. At pH of 4.0−5.0, Al(III) precipitated and transferred into Al(OH) 3 with a flocculent amorphous morphology. Active sites on the Al(OH) 3 surface enhanced the removal efficiency of P507. At pH of 6.0−6.5, Al(III) and Mg(II) formed layered crystalline Al(OH) 3 and MgAl 2 (OH) 8 with small pore channels and fewer active sites, resulting in a reduced removal efficiency of P507. When the Al/P molar ratio exceeded 13 and the pH was between 4.0 and 5.0, the removal rates of both Al(III) and P507 were higher than 98%, while the concentration loss of Mg(II) was only 0.2%−0.9%.

CAS / MDL: 7784-13-6
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JOURNAL OF FOOD COMPOSITION AND ANALYSIS · 2024 · IF 4

Development of Al-MOF based pipette-tip solid-phase extraction approach for detection of fluoroquinolones in animal innards

Shumin Lin,Xiaoyu Zhang,Xiliang Li,Shu-xuan Liang

Residues of fluoroquinolones (FQs) have been identified as a threat to food safety, highlighting the need for effective detection methods in food samples. This study utilized a hydrothermal synthesis method to create Al-based metal-organic framework (Al-MOF) for pipette-tip solid-phase extraction of FQs in food matrices. Coupled with HPLC-FLD, a novel sample pretreatment method for simultaneous detection of three FQs was developed, demonstrating good linearity (1−500 ng/g) with R 2 values ranging from 0.9990 to 0.9998. Limits of detection and quantification were found to be 0.15−0.25 ng/g and 1.0−2.0 ng/g, respectively, with the relative standard deviations below 9.3 %. The extraction method showed promising results in animal liver and kidney samples, with a recovery rate of 75.2−103.6 %. Overall, this simple, rapid, and efficient method offers a valuable approach for analyzing trace levels of FQs in complex matrices.

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FATIGUE & FRACTURE OF ENGINEERING MATERIALS & STRUCTURES · 2024 ·Vol. 47 ·期 8 ·2905-2921 · IF 3.1

Fatigue life assessment of carbon nanotubes reinforced Al-Cu-Mg composite foams via statistics analysis and computer vision

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.

CAS / MDL: 7704-98-5
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JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY · 2025 · IF 2.4

Heterogeneous catalyst of cobalt phthalocyanine tetrasulfonamide loaded on Ca–Al hydrotalcites for oxidative desulfurization of spent sulfidic caustic

Ruiqi Huang,Zhaoyang Lu,Can Xu,Shuaiting Liang,Honglei Yuan,Geshan Zhang,Lihui Jia,Jun Yuan

Background Spent sulfidic caustic (SSC) from petrochemical and other chemical industries usually contains high concentrations of sulfur ion (S 2− ) and caustic soda (NaOH), which requires effective treatment. Here a CoPcSA/CaAl-LDHs catalyst was successfully synthesized by using a facile one-pot approach for loading cobalt phthalocyanine tetrasulfonamide (CoPcSA) on Ca–Al hydrotalcites (CaAl-LDHs). The material characterization included powder X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy and X-ray photoelectron spectroscopy. Results The effect of various parameters such as reaction temperature, catalyst dosage and aeration rate on the catalytic activity was investigated and optimized to be 75 °C, 1.5 mmol L −1 and 2.5 L min −1 , respectively. CoPcSA/CaAl-LDHs shows very high catalytic efficiency for S 2− removal: a 95.0% S 2− removal can be achieved at extremely high concentration of S 2− (24 000 mg L −1 ). In addition, the catalyst exhibits high stability and reusability even after 8 cycles of reuse. Conclusion CoPcSA/CaAl-LDHs exhibits outstanding catalytic activity and stability, showing impressive potential in practical application. © 2025 Society of Chemical Industry (SCI).

CAS / MDL: 3317-67-7
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JOURNAL OF MEMBRANE SCIENCE · 2024 · IF 8.4

High performance Zn–Al LDH modified forward osmosis membrane with antibacterial, anti-membrane fouling, and photocatalytic degradation ability

Yifan Wang,Tingjuan Wang,Xiaowen Wu,Jiancheng Wang,Endong Chang,Zhaohui Huang,Minghao Fang,Xin Min,Shiming Su

Forward osmosis membrane has shown great potential in the fields of seawater desalination and sewage treatment. However, the concentration polarization phenomenon and membrane fouling in the water treatment process greatly reduce the water treatment performance and restrict its application. To address these challenges, we employed a pre-buried seed-in-situ growth method to facilitate the Zn–Al layered double hydroxide (Zn–Al LDH) growth on the thin nanofiber membrane, and use it as the support layer for the preparation of a Zn–Al LDH modified forward osmosis membrane. Studies have shown that the introduction of Zn–Al LDH significantly improves the water treatment efficiency of the forward osmosis membrane (In Al-DS mode, the water flux increased by 87.5 %, up to 50.50 LMH, with a low specific salt flux of 0.13 g L −1 ). It also exhibits exceptional antibacterial, anti-membrane fouling, and photocatalytic degradation properties. This research presents a novel approach for the development of advanced high-efficiency forward osmosis membranes.

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COMPOSITES COMMUNICATIONS · 2024 · IF 6.5

Facile synthesis of NH2-MIL-53(Al)@BiOBr@CQDs ternary heterostructure photocatalyst for degradation of ciprofloxacin in water

Xinyue Yang,Yong Li,Deyun Yue,Rui Li,Haojie Song

The construction of ternary heterojunction photocatalysts can achieve multi-gradient transfer of charges and accurate control the position of photogenerated electrons which has received increasing attention. In this paper, NH 2 -MIL-53(Al)@BiOBr@CQDs-10 % (ABCQDs-10 %) was prepared via a facile hydrothermal and chemical synthesis processes. Three-dimensional serration of NH 2 -MIL-53(Al) as a platform for irregular BiOBr nanosheets, CQDs promote interfacial contact and act as electron transport channels between BiOBr and NH 2 -MIL-53(Al) and constitute Z-type heterojunctions with high redox properties. ABCQDs-10 % shows the best photocatalytic removal efficiency (94.24 %) of CIP, the reaction rate constants (0.045 min −1 ) were 1.2 and 64 times higher than BiOBr and NH 2 -MIL-53(Al), respectively. The excellent degradation performance is attributed to the construction of Z-type heterojunction of NH 2 -MIL-53(Al)@BiOBr@CQDs which improve electron-hole separation and transfer efficiency. The main active species was •O 2 - . The photocatalytic activity of ABCQDs-10 % had not obvious loss after cycle experiments and the crystal structure had no significant changes, means high stable photocatalytic activity.

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Materials Today Communications · 2024 · IF 3.7

Improve mechanical properties and corrosion resistance of Al/Sn heterogeneous joints by ultrasonic-assisted liquid phase diffusion bonding

Pu Zhao,Zhengwei Li,Zhiwu Xu,Xuesong Liu,Jiuchun Yan

How to obtain a high-strength and corrosion resistance of Al/Sn/Al joint has been a longstanding goal for electronics industry. In this work, 6063Al was joined in the air by ultrasonic-assisted liquid phase diffusion bonding using a Sn filler metal . It was performed by applying an uninterrupted ultrasonic vibration at a heating temperature of 360 ℃, final obtaining a 6063Al joint without enriched-Sn. Under the action of ultrasonic vibrating, the breaking of oxide film , the diffusing of Sn, and dissolving of Al alloy occurred in sequence. It resulted in a transition of bonding interface from Sn/Al to an α-Al/α-Al bonding interface embedded a few Mg 2 Sn partials, after depleting Sn by grain boundary diffusion . The joints possessed a high strength coefficient of 86.7% of 6063Al base metal and 161.8% of soldering joint. The joint had a better corrosion resistance that the tensile strength only reduced 35.3% after a corroding of 72 h in 3.5 wt% NaCl solution in comparison with the soldering joints. Finally, the evolution of the interface structure and mechanism of improving corrosion resistance were discussed in detail. It is a promising technology for manufacturing high-reliable Al/Sn heterogeneous joints.

CAS / MDL: 7647-14-5 7732-18-5
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