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CHEMICAL ENGINEERING JOURNAL · 2023 · IF 15.1

Self-destructive microchip: Support-free energetic film of BiOBr/Al/Bi2O3 nanothermites and its destructive performance

Haifeng Yang,Zhiqiang Qiao,Weimiao Wang,Pengfei Tang,Shuaishuai Man,Xiaodong Li,YuTing Xie,Deyun Tang,Xueming Li,Guangcheng Yang

Private information protection of electronic chips which store large amounts of sensitive data, is a crucial issue in electromechanical systems nowadays. Here, a self-destructive microchip based on an instantaneous thermite reaction is designed to prevent the leakage of electronic information. The device is consisted of a silicon test wafer and an upper energetic film coated by a simple drop-casting technique. A series of Al/BiOX-based nanothermites have been prepared for decreasing the reaction sensitivity, meanwhile optimizing the destruction efficiency of the energetic film system. Among them, Al/Bi 2 O 3 nanothermite containing 30 wt% BiOBr possesses a low sensitivity (45 J), the maximum pressure peak (1.93 MPa) and pressure effect duration due to multiple interactions of the three nano-scale energetic components. Besides, the energetic film prepared by this nanothermite fomula also exhibits a more effective destruction of the device. The high-speed photography results demonstrate that the violent reaction shatters the thick energetic microchip (∼1 mm) within merely 0.5 ms. Importantly, the efficient destruction of energetic microchips shows excellent reproducibility in different working scenes, including Air or Ar atmosphere. It is believed that this self-destructive device with environmentally friendly components and simple but adaptive design can be extensively used in various electric microcomponents.

CAS / MDL: 69-65-8
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CHEMOSPHERE · 2022 · IF 8.943

Micro-electrolysis based nitrate reduction from aqueous solution by CNTs-Al-Cu composite under alkaline environment

Zhiyu Wei,Jie Chen,Hongjin Tong,Mingchao Sun,Jing Tian,Lu Fan

CNTs-Al was prepared by ball milling combined with sintering process and then used for CNTs-Al-Cu synthesis with chemical deposition method. The obtained CNTs-Al-Cu composite was systematically characterized and its NO 3 − -N reduction performance under alkaline condition was also evaluated. As indicated by the reduction batch experiment, 80.2% of NO 3 − -N removal efficiency was obtained in 90 min at pH of 9. The product of the reduction process was dominated by NO 2 − -N, which was further reduced to harmless N 2 . The reusability of CNTs-Al-Cu composite was evaluated, and the experiment results showed that 68.1% of NO 3 − -N removal efficiency was maintained after 3 cycles of regeneration. Finally, based on the characterization results and kinetic analysis, it was concluded that micro-electrolysis was mainly responsible for the removal of NO 3 − -N by CNTs-Al-Cu.

CAS / MDL: 7429-90-5 25322-68-3
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LANGMUIR · 2022 · IF 4.331

Graphdiyne (CnH2n–2)-Based GDY/CuI/MIL-53(Al) S-Scheme Heterojunction for Efficient Hydrogen Evolution

Zhiliang Jin,Xiaohong Li,Teng Li,Youji Li

Graphdiyne (g-CnH2n–2) is a new carbon material composed of sp and sp2 hybrid carbon atoms. Since the synthesis by Li’s team, graphdiyne has been widely studied in other fields because of its excellent properties. In this paper, graphdiyne was synthesized from copper-containing materials and the composite GDY/CuI/MIL-53(Al) S-scheme heterojunction is prepared for photocatalytic cracking of water to produce hydrogen. First, GDY/CuI was prepared by organic synthesis, and then GDY/CuI was anchored on the surface of MIL-53(Al) by in situ ultrasonic stirring. After the continuous optimization of experimental conditions, the final hydrogen evolution rate is much higher than that of MIL-53(Al). This efficient photocatalytic performance can be attributed to the S-scheme heterojunction formed by the unique energy band arrangement. At the same time, the mechanism of charge transfer was demonstrated by in situ irradiation X-ray photoelectron spectroscopy. The strong interaction among the three strongly promotes the separation and transfer of photogenerated electron–hole pairs.

CAS / MDL: 100-21-0
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Coatings · 2023 ·Vol. 13 ·期 7 ·1246 · IF 3.4

Production of Al–Mn/WC Composite Coatings with Electrodeposition in AlCl3–NaCl–KCl–MnCl2 Molten Salts

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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CHEMICAL ENGINEERING JOURNAL · 2023 · IF 15.1

Al-doped CuS/Znln2S4 forming Schottky junction induced electron trap centers for photocatalytic overall water splitting

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.

CAS / MDL: 68-12-2
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NEW JOURNAL OF CHEMISTRY · 2022 ·Vol. 47 ·期 1 ·109-119 · IF 3.925

Removal of uranium from wastewater through Ni–Al-layered double hydroxide@carbon nanotubes functionalized by polyethyleneimine

Debin Ji,Yao Liu,Xuepeng Wang,Zhiqiang Qiao,Jialiang Yang,Ziheng Bai,Shuxia Guan,Zhandong Li,Hongjun Wu,Yongde Yan

Nuclear energy is widely used as an efficient energy. However, the production of a large amount of uranium-containing wastewater is considerably harmful to the environment. Adsorption is a commonly used method for removing uranium ions from water. In this study, carbon nanotubes (CNTs) were first modified with polyethyleneimine (PEI), and then Ni–Al-layered double hydroxide (LDH) was anchored to CNT-PEI (CNT-P) by using the co-precipitation method to obtain CNT-P/LDH (NO3−). The experimental results indicated that the adsorption process was consistent with Langmuir kinetic adsorption and Sips adsorption isotherm models at the pH of 6. The fit result of the Sips adsorption isotherm model indicated that the adsorption capacity of CNT-P/LDH was 646.6 mg g−1. XPS analyses showed that the adsorption of uranium on CNT-P/LDH mainly involved three aspects. Tests were conducted for different salinities, and the results showed a uranium removal rate of >95% at a salinity of 3.5%.

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FUEL · 2022 · IF 8.035

Study of ignition and combustion characteristics of kerosene-based nanofluid fuel containing n-Al/CuO thermite

Xiang Lv,Yi Gao,Yueshuai Cui,Chen Wang,Gangchui Zhang,Fang Wang,Peijin Liu,Wen Ao

The ignition and combustion properties of n -Al/CuO/kerosene nanofluid fuels are examined, with a focus on the formulation effects of the n -Al/CuO nano-thermite. The DSC data shows the addition of CuO facilitates the exothermic process of n -Al particles, which then promote the n -Al/CuO/kerosene droplets to evaporate. There are two exothermic peaks on the DSC curve of n -Al/CuO (5 %) at 249.3 ℃ and 463.8 ℃, respectively. The burning of n -Al/CuO/kerosene droplets consists of four stages: ignition, d 2 -law combustion, vapor flame extinguishment, and agglomerate burning. During the agglomerate burning stage, n -Al/CuO (5 %)/kerosene shows the minimum ignition delay at 0.057 s and the highest emission spectral intensity. Droplet combustion conforms well to the d 2 -law, and the maximum combustion rate is found for n -Al/CuO (20 %)/kerosene, at 1.287 mm 2 s −1 . The particle size of combustion residues is uniform, and the overall appearance smoothens as the CuO content increases. A new nanofluid fuel with better ignition and combustion properties than traditional nanofluid fuels is proposed.

CAS / MDL: 1317-38-0 53363-87-4
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MINERALS ENGINEERING · 2022 · IF 5.479

Improve the durability of lithium adsorbent Li/Al-LDHs by Fe3+ substitution and nanocomposite of FeOOH

Qinglong Luo,Mingzhe Dong,Quan Li,Zhijian Wu,Zhong Liu,Jun Li

The selective extraction of lithium from brine by lithium aluminum layered double hydroxides (Li/Al-LDHs) adsorption is used industrially. To maintain the structural and performance stability of the Li/Al-LDHs adsorbent, the Li/Al-LDHs adsorbent can be doped with some high electron density metals such as Fe(III) and regenerated by dilute Li-containing aqueous solution. In this study, we use Fe(III) doping and FeOOH nanocomposite to stabilize the structure of Li/Al-LDHs. The nanocomposites of Li/Al-LDHs, Fe dopped Li/Al-LDHs (Fe-Li/Al-LDHs), and FeOOH were synthesized by the phase-separated sol–gel method and granulated by using crosslinked alginate polymers. The nanocomposites and granulated nanocomposites were characterized by SEM, TEM, XPS, FT-IR, and XRD analyses. The adsorption–desorption performance of the granulated nanocomposites was evaluated with a single LiCl solution and the brine from Da Qaidam Salt Lake. The isotherms, kinetics, and thermodynamics parameters and Arrhenius parameters of the lithium adsorption of the granulated nanocomposites were obtained. At the 80% mass loading of the nanocomposites in the granulation, the granulated nanocomposites statically adsorbed 9.46 mg/g lithium and dynamically 8.18 mg/g lithium from Da Qaidam Salt Lake brine. The Fe(III) doping and nanocomposite with FeOOH reduced the dissolution of the Li/Al-LDHs in the granulated nanocomposites and did not negatively affect the adsorption capacity of the granulated nanocomposites.

CAS / MDL: 57-13-6 9005-38-3
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RENEWABLE ENERGY · 2022 · IF 8.634

Alloying cobalt in Co–Fe–Al catalyst for achieving the selective conversion of furfural to cyclopentanone

Yuewen Shao,Jie Wu,Zhiyuan Zheng,Mengjiao Fan,Kai Sun,Félix Mérimé Bkangmo Kontchouo,Lijun Zhang,Shu Zhang,Guangzhi Hu,Xun Hu

Production of cyclopentanone (CPO) from biomass-derived furfural is attractive but challenging, as deep hydrogenation or ring-opening of furan ring in furfural over Co-based catalysts hinders the formation of the targeting products. In this study, alloying Co with Fe species in Co–Fe–Al catalysts is proposed for selective conversion of furfural to CPO in water. The formation of CoFe alloy in Co–Fe–Al catalyst weakened the interaction between Co species and the alumina carrier, lowered the adsorption/activation of H 2 , suppressed the formation of especially Brønsted acidic sites, facilitated the electron transfer from Co 0 to Fe species, increased the activation energy for hydrogenation of furfural (from 17.2 kJ mol −1 over Co–Al to 33.4 kJ mol −1 over 1.5Co-1.5Fe-1.0Al), and weakened the adsorption of C C and C–O–C functionalities in furan ring of furfuryl alcohol (FA) on metallic sites. These factors together suppressed deep hydrogenation of furan ring in FA or ring-opening of FA to diols, producing CPO and CPL with total yield of 91.5%, which was attributed to the synergy between hydrogenation and Brønsted acidic sites. In addition, the presence of Fe in Co–Fe–Al catalysts also enhanced the structural stability of Co species, preventing the phase transformation and aggregation of Co species, and rendering the catalyst with superior reusability .

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WATER RESEARCH · 2022 · IF 13.4

Variations in NOM during floc aging: Effect of typical Al-based coagulants and different particle sizes

Junjie Yu,Hui Xu,Dongsheng Wang,Hongyan Sun,Ruyuan Jiao,Yang Liu,Zhiyuan Jin,Shuo Zhang

Most studies on the interaction between coagulation and NOM (natural organic matter) currently focus on pollutant removal and coagulant species distribution, while studies on floc aging are lacking. Investigation onto the effects of floc aging could guide further processes that utilize flocs, such as densadeg sludge recirculation, floc predeposition for ultrafiltration, sludge condensation, and other traditional sludge reflux processes. In this study, flocs generated by Al 13 and AlCl 3 in microparticle- and nanoparticle-containing water were investigated, and the effect of floc aging on NOM was quantified based on several organic matter characterization techniques. Flocs absorb and release organics during aging. The flocs generated from micro-SiO 2 have a significant absorbing effect for LWM-N (low-molecular-weight neutral substances) and protein-like substances, while the absorption of NOM by flocs generated from nano-SiO 2 is insignificant. HS (humic substances) with high aromaticity are released during floc aging. From the molecular perspective, the molecules released during floc aging are those with higher double bond equivalents and higher aromaticity, while the absorbed molecules are those with lower double bond equivalents and lower aromaticity. 2D-COS (two-dimensional correlation spectroscopy) demonstrated that the flocs generated by Al 13 and AlCl 3 had the same organic release patterns but different intensities, while the flocs generated in the micro-SiO 2 and nano-SiO 2 systems had different organics release patterns. Abundant aluminum hydrolysates with low polymerization and amorphous Al(OH) 3 would be produced from AlCl 3 during the coagulation process and then undergo hydroxyl‑bridging reaction and crystallization during floc aging, thus releasing more HS with high aromaticity into the supernatant; in comparison, prehydrolyzed Al 13 produces a more stable floc and releases less HS during aging. The flocs produced by nano-SiO 2 and Al-based coagulants release higher aromaticity HS into the water than those produced by micro-SiO 2 , which may be related to the formation of more highly polymerized degree hydrolysates and nanocrystalline Al(OH) 3 in the nano-SiO 2 system. The flocs generated in water with micro-SiO 2 may contain a large amount of Al-OH and have a loose structure, thus further absorbing NOM, such as protein-like substances and LWM-N. In contrast, the flocs generated from nano-SiO 2 possess abundant adsorbed water and a denser structure; thus, organic matter cannot be absorbed stably.

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OPTICAL MATERIALS · 2022 · IF 3.754

Novel In2S3/Zn–Al LDHs composite as an efficient visible-light-driven photocatalyst for tetracycline degradation

Man Wang,Jun Wang,Mengjun Li,Xinru Wang,Yating Sima,Qiang Wu

Hexagonal Zn–Al hydrotalcite (Zn–Al LDHs) has become a research hotspot in the field of photocatalysis due to efficient photocatalytic performance, low cost and non-toxicity. In this research, In 2 S 3 /Zn–Al LDHs composites were firstly synthesized by one-pot method with InCl 3 and TAA as raw materials. The crystalline structure, surface morphology , chemical composition, together with optical properties of the samples were investigated by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectra (FT-IR), UV–Vis diffuse reflectance spectrometry (DRS), and Photoluminescence spectra (PL). The photocatalytic performance of the composite photocatalyst was investigated by degradation of tetracycline (TC) under visible-light irradiation. The photochemical properties and cyclic stability of the photocatalyst were further explored. Experimental results display that the photocatalytic efficiency of In 2 S 3 /Zn–Al LDHs (1:2) was remarkably superior to that of pure In 2 S 3 and Zn–Al LDHs. In 2 S 3 /Zn–Al LDHs (1:2) composite showed high photocatalytic activity for TC degradation (92.2% within 30 min). The modification of Zn–Al LDHs by In 2 S 3 prompted the separation of photogenerated electron-hole pairs and thus improved the photocatalytic performance. It can be inferred that the efficient photocatalytic performance of In 2 S 3 /Zn–Al LDHs composites could remove many hazardous pollutants in wastewater.

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JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY · 2022 · IF 6.76

Facile microwave-assisted solvothermal synthesis of rod-like aluminum terephthalate [MIL-53(Al)] for CO2 adsorption

Liwei Sun,Meilin Yin,Zhen Li,Shaokun Tang

To alleviate environment issues derived from CO 2 emission, developing effective and economical methods for CO 2 capture has attracted much attention for decades. Metal-organic frameworks possess high porosity and stability, which is favorable to the adsorption of small molecules. Herein, an aluminum-based MOF, aluminum terephthalate [MIL-53(Al)], was synthesized with H 2 O and N , N′ -dimethylformamide as co-solvent via microwave-assisted method for CO 2 adsorption. The parameters including pre-mixing mode, microwave temperature, microwave power and reaction time were varied to study their influences on crystal structure, morphology and CO 2 adsorption capacity of MW-MIL-53(Al). Wherein, MW-MIL-53(Al) prepared with pre-mixing mode of stirring at 130 °C, 200 W and 3 h presents high crystallinity and rod-like morphology. The synthesized MW-MIL-53(Al) possesses relatively high BET surface area (961 m 2 /g), pore volume (0.46 cm 3 /g) and thermal stability (up to 480 °C), and its CO 2 adsorption capacity is 2.16 mmol CO 2 /g adsorbent under 25 °C and 0.1 MPa, which is higher than CS-MIL-53(Al) synthesized via conventional solvothermal method at 130 °C for 48 h.

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