FOOD CHEMISTRY
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2023
·
IF 8.8
Huilin Li,Jingying Yang,Ran Han,Yueyao Wang,Xintong Han,Shuo Wang,Mingfei Pan
Rapid, sensitive, specific and stable detection of mycotoxin in food remains an extremely crucial issue. Herein, a magnetic-fluorescent immunosensing platform for the detection of zearalenone (ZEN) was proposed. The platform utilized Au nanoparticles (AuNPs) heterogeneous fluorescent metal–organic framework (MIL-53(Al)@AuNPs) labeled with ZEN-bovine serum albumin (ZEN-BSA) as signal probe and ZEN mono-antibodies coupled with magnetic NPs (MNPs-mAbs) as capture probe. Specifically, the heterogenization of AuNPs on the MIL-53(Al) surface improved its biocompatibility, and facilitated the loading of ZEN-BSA conjugates. The MNPs-mAbs could rapidly capture the target ZEN, simplify the immunoassay process and further improve the detection efficiency. The established competitive magnetic-fluorescent immunosensing platform had a wider linear response to ZEN in the range of 0.001–100 ng/mL with a lower limit of detection (LOD) at 0.0035 ng/mL, and could finish the whole detection process within 20 min, showing great potential for rapid and sensitive detection of food contaminants.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2023
·
IF 6.2
Wei Le,Wanjun Zhao,Yanli Zhu,Xin Zeng,Dazhi Liu,Qingjie Jiao
Aluminum (Al)-lithium (Li) alloys are ambitious candidates for application in energetic materials, however, the high reactivity of Al-Li compound and Li in alloys affects their thermal stability, which results in gradually lower active content and diminished performance, impeding their further application in energetics. In this study, the specific content of silicon (Si) was introduced into Al-Li alloy via the centrifugal atomization that allows in-situ assembly of Al , Li, and Si at the single particle level, thus resulting in more stable Al-Li-Si compounds instead of active Al-Li compounds and Li and enhancing their thermal stability. The results show that Al-Li-Si alloy powders are in a high degree of sphericity, which are composed of αAl and AlLiSi. Compared to Al-Li alloys, Al-Li-Si alloys initiate the oxidization at a higher temperature (∼600 ℃) since the existence of more stable Al-Li-Si compounds than Li in Al-Li alloys, which indicates a higher thermal stability. Al-Li-Si alloys also show high heat release and combustion efficiency similar to Al-Li alloys. In the meanwhile, Al-Li-Si alloy-based composites maintain almost the same combustion properties compared to Al-Li/PTFE energetics, along with prolonged combustion duration. Therefore, Al-Li-Si alloy powders are promising candidates for application in energetic materials considering their higher thermal stability and tunable combustion properties.
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Coatings
·
2023
·Vol. 13
·期 7
·1246
·
IF 3.4
Wenjuan Qi,Desheng Ding,Weijie Luo,Weiliang Jin,Qian Kou,Chuntao Ge,Saijun Xiao
The hardness and wear resistance of amorphous Al–Mn alloy coatings can be improved by incorporating ceramic particles into them to extend their application. In this paper, Al–Mn/WC composite coatings have been prepared with electrodeposition in stirred AlCl3–NaCl–KCl–MnCl2molten salts at 180 °C with the addition of WC particles. The effects of stirring speed (400–700 rpm) and cathode current density (15–75 mA/cm2) on the produced Al–Mn/WC composite coatings have been studied. At 600 rpm and 700 rpm, the Al–Mn/WC composite coatings exhibited the best uniform distribution of the embedded WC particles, with the tested microhardness value up to 650 HV0.1, compared with 530 HV0.1of the Al–Mn alloy. Moreover, under various cathode current densities, the best quality of the Al–Mn/WC composite coating was obtained at 55 mA/cm2, with a homogeneous distribution of WC particles and the highest microhardness value (670 HV0.1). It is expected that this method could be extended to be applied for the preparation of aluminum-based and magnesium-based ceramic composite coatings.Keywords:AlCl3–NaCl–KCl–MnCl2molten salts;electrodeposition;WC particles;Al–Mn/WC composite coating
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IONICS
·
2023
·Vol. 29
·期 7
·2853-2864
·
IF 2.8
Wang Wenping,Zhao Zhiyi,Deng Jiayao,Lang Wei,Zhen Lipeng,Lu Huimin
The oxygen reduction reaction of the cathode in an Al-air battery plays a key role in the performance of the entire battery. Generally, Pt and its alloys are recognized as catalysts with high oxygen reduction catalytic performance, but their application is limited by the rare earth content and high cost. In this paper, α-MnO 2 nanotubes are prepared using a hydrothermal method and used as a template. Nano-Ni–Mn bimetallic oxides with different compositions are prepared with different NiO and α-MnO 2 ratios by calcination. The effects of morphology, phase, and Mn 3+ /Mn 4+ and Ni 3+ /Ni 2+ ratios on electrochemical performance and battery discharge performance are analyzed. The results show that the contents of α-MnO 2 and Ni 6 MnO 8 in NM-12 catalyst are low, and the molar ratio of Mn 3+ /Mn 4+ and Ni 3+ /Ni 2+ is high. Also, the specific surface area of NM-12 is relatively high. Finally, the catalyst prepared with a NiO to α-MnO 2 ratio of 1:2 shows better electrochemical catalytic performance and battery discharge performance that is comparable to that obtained for a commercial 20 wt% Pt/C catalyst.
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CHEMICAL ENGINEERING JOURNAL
·
2023
·
IF 15.1
Yachao Xu,Zhong Zhou,Peng Yu,Ying Wang
Synergistically tuning electronic states at the atomic level to facilitate photocatalytic overall water splitting is a challenge. However, elucidation of the role of specific electronic states of Znln 2 S 4 (ZIS) in regulating both the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER) is still scarce, making it difficult to accurately predict the actual photocatalytic performance. Here, the substitution of Zn sites with Al atoms was found to modulate the potential difference of the ZIS surface domain heterojunction structure, and electrons were further transferred to CuS to form a built-in field that promotes charge separation. When Al doping is present on the ZIS surface, ZIS exhibits p-type semiconductor properties, which leads to the formation of p-n junctions within Al-CuS/ZIS itself. Due to the large work function and metallic properties of CuS, and Al-CuS/ZIS as a whole tends to form a Schottky heterojunction, and the two heterojunction structures synergistically promote the migration of photogenerated carriers. In addition, the Al doping changes the electronic states around the ZIS, allowing the Al ZIS to promote the adsorption of O* and H* during OWS. The solar-driven photocatalytic overall water splitting efficiency of Al-CuS/ZIS is as high as 153.6 (HER) and 73.1 (OER) μmol/h g −1 , which is about 10 times that of ZIS. This work opens the possibility to design efficient photocatalytic materials through tunable composition and electronic structure.
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Nanomaterials
·
2023
·Vol. 13
·期 12
·1837
·
IF 5.3
Miaomiao Jin,Zhanxin Song,Wei Liu,Guozhen Wang,Mo Xian
Biological approaches for the synthesis of a hybrid explosive–nanothermite energetic composite have attracted greater scientific attention because of their advantages, including their moderate reactions and the absence of secondary pollution. In this study, a simple technique was developed to fabricate a hybrid explosive–nanothermite energetic composite based on a peptide and a mussel-inspired surface modification. Polydopamine (PDA) was easily imprinted onto the HMX, where it maintained its reactivity and was capable of reacting with a specific peptide used to introduce Al and CuO NPs to the surface of the HMX via specific recognition. The hybrid explosive–nanothermite energetic composites were characterized using differential scanning calorimetry (TG-DSC), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy(XPS), and a fluorescence microscope. A thermal analysis was utilized to investigate the energy-release properties of the materials. The[email protected]@CuO, which benefitted from an enhanced interfacial contact in comparison with the physically mixed sample (HMX-Al-CuO), demonstrated a 41% lower HMX activation energy.Keywords:biological self-assembly;polydopamine;peptide;green preparation;activation energy
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SCIENCE OF THE TOTAL ENVIRONMENT
·
2023
·
IF 9.8
Yong Zhang,Siqi Huang,Bingyu Mei,Lingyi Jia,Jun Liao,Wenkun Zhu
A novel dopamine-supported Mg( Ca )Al layered double hydroxide composite was synthesized by co-precipitation method. The existence of Ca 2+ and dopamine could promote the capture of uranium on the layered double hydroxides. In batch experiments, the composite exhibited good uranium removal performance, including high adsorption capacity (687.3 mg/g), strong anti-interference and good reusability (the removal percentage was still higher than 90 % after five cycles). At low initial uranium concentration, the uranium removal percentage on the composite exceeded 99.7 % and the residual concentration of uranium in the solution was <0.03 mg/L, reaching the limited standard of the World Health Organization. The studies of adsorption kinetics and isotherm indicated that the uranium adsorption behavior on the composite conformed to the pseudo-second-order kinetic and Langmuir isotherm models, suggesting that the process was a monolayer adsorption dominated by chemical adsorption. Furthermore, the high-efficiency uranium adsorption on the Mg( Ca )Al layered double hydroxide was mainly attributed to the strong complexation between the active sites (-OH and -NH 2 ) and uranium, the precipitation of interlayer intercalation ions (CO 3 2− and OH − ) to uranium and the ion exchange of Ca 2+ to uranium. Due to these advantages, the dopamine-supported Mg( Ca )Al layered double hydroxide composite is expected to be used as fine adsorbent to remove uranium from wastewater.
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MATERIALS CHARACTERIZATION
·
2023
·
IF 4.7
Chengyi Xu,Xiaoping Cai,Xinyang Jiao,Khanh Ly Vu,Zhichao Shang,Peizhong Feng
Porous CoAl 3 intermetallics have great catalytic potential. However, its high porosity and controllable preparation are still incipient. In this paper, the effect of isothermal treatment on the near-net formation process of porous CoAl 3 material is studied, and the phase transformation process and diffusion kinetics of the Co/Al diffusion couple in the solid-phase diffusion stage are described. The results show that isothermal treatments in the range of 510–550 °C reduce the exothermic intensity of the thermal explosion (TE) reaction. The holding time of 30 min at 530 °C facilitates the near-net formation of porous CoAl 3 . The isothermal treatment does not affect the phase composition of the final product. Still, it causes changes in the phase and depth of the diffusion, affecting the exothermic strength and skeleton morphology. Based on the phase transition and thermodynamic analysis , the CoAl phase formation is the key to reducing the exothermic intensity. The diffusion kinetics indicates that the low diffusion activation energy of the CoAl phase (Q 1 = 1.66 kJ mol −1 ) is the main reason for the preferential formation. And the exponential kinetic factor of the second diffusion layer (n 2 = 0.75) explains its high diffusion depth.
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CARBOHYDRATE POLYMERS
·
2018
·
IF 5.158
Wenbin Hu,Lingbin Lu,Zhanying Li,Lin Shao
Bulk Al-doped carboxymethyl cellulose aerogels were obtained via a facile slow-gel method and freeze-drying technology. In this method, the cross-linker Al 3+ was released slowly and completely with enough d -(+)-gluconic acid δ -lactone as a sustained-release agent. Depended on controlled releasing of Al 3+ , the reaction speed between Al 3+ and carboxyl groups was controlled and Al 3+ was well-distributed in the aerogels. The coordination type between Al 3+ and carboxymethyl cellulose was the bidentate bridging coordination. By adjusting the amount of Al 3+ and the degree of substitution of carboxymethyl cellulose, interconnected network and closely packed sheet-like structure presented, respectively. According to the nitrogen adsorption-desorption isotherms, the aerogels were a kind of mesoporous material with pore blocking or cavitation. In addition, the aerogels exhibited outstanding weight-bearing capacity and excellent flame retardancy. This work provided a valuable reference for doping metal ions into polysaccharide aerogels and expanding the application fields of aerogels.
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CERAMICS INTERNATIONAL
·
2019
·
IF 3.45
Hang Liu,Shengqiang Song,Andrie M. Garbers-Craig,Zhengliang Xue
Cr 2 O 3 is a well-known corrosion resistant oxide used in refractory applications. However, it can oxidize into toxic and water-soluble Cr(VI) compounds upon reaction with calcium aluminate cement phases in the presence of oxygen, which subsequently causes disposal problems after use. This study describes the extent to which chromium in the spinel Mg(Al,Cr) 2 O 4 phase can be oxidized to Cr(VI) when it reacts with the calcium aluminate cement phases C 12 A 7 , CA, CA 2 and free CaO at 1300 °C in air, using XRD, XPS and leaching tests (TRGS 613 standard) as analytical tools. On reaction with CaO, the Mg(Al,Cr III ) 2 O 4 spinel mainly transformed into hauyne (Ca 4 Al 6 Cr VI O 16 ) and Ca 5 Cr 3 O 12 which contains both Cr(IV) and Cr(VI). The reaction of C 12 A 7 and CA with the spinel phase also resulted in the formation of Ca 4 Al 6 CrO 16 . Conversely, the reaction of Mg(Al,Cr III ) 2 O 4 spinel with CA 2 resulted in the formation of only a trace amount of Cr(VI). Water-soluble Cr(VI) leached in large quantities (>100 mg/L) from samples where the Mg(Al,Cr III ) 2 O 4 reacted with either C 12 A 7 or CA. Almost no Cr(VI) leached from the sample when Mg(Al,Cr III ) 2 O 4 reacted with CaO, using the standard TRGS 613 leach test, but a significant amount of Cr(VI) was released into solution when leached with a HCl solution for 12 h. Both Cr(IV) and Cr(VI) present in the Ca 5 Cr 3 O 12 dissolved into acidic solution. Only a small amount of Cr(VI) leached from the sample that resulted when spinel was reacted with CA 2 , even after a prolonged HCl leach. Cr(III) in spinel Mg(Al,Cr) 2 O 4 is very stable and does not leach in either distilled water or acidic solution.
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JOURNAL OF THE ELECTROCHEMICAL SOCIETY
·
2019
·Vol. 166
·期 2
·D65
·
IF 3.12
Min Li,Ying Li,Zhaowen Wang
The electrochemical reduction of zirconium oxide in a molten salt of 2.4NaF·AlF3 (molar ratio = 2.4) was studied at 1273 K. Cyclic voltammetry results show that Zr(IV) ions are first reduced to an intermediate valence and, then, are co-deposited with aluminum to form an Al-Zr alloy. Potentiostatic electrolysis experiments were carried out at different potentials (−0.95 and −1.25 V) and at 1273 K, and the electrolysis products were characterized using SEM-EDS and XRD. The XRD analysis confirms that a mixture of cryolite molten salt and ZrO2 was electrodeposited at −0.95 V, while aluminum and Al3Zr were electrodeposited at −1.25 V. The SEM analysis shows that the aluminum and Al3Zr were in two different phases.
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POLYHEDRON
·
2019
·
IF 2.284
Ning Tian,Yifang Dai,Qing Liu,Wei Dai
A general synthetic strategy for HS-Fe 3 O 4 @MIL-53(Al) adsorbent has been developed in this work. The composite material exhibits an efficient capture performance for rubidium ion due to sulfhydryl group and magnetic Fe 3 O 4 doped in its porous cavity. The results of X-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, and N 2 adsorption–desorption proved that the HS-Fe 3 O 4 was immobilized in the composite material. High Rb + uptake capacity over the HS-Fe 3 O 4 @MIL-53(Al) is attributed to the exchange of acidic protons between the sulfhydryl group and the Rb + . The pseudo-second-order and Freundlich model could make a good description of the adsorption process. The Rb + sorption selectivity was moderately influenced by any co-ions effect (K + , Na + and Cs + ) due to HS-Fe 3 O 4 doped. These results reveal that our novel composite material might be a promising industrial adsorbent for Rb + capture.
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