FUEL PROCESSING TECHNOLOGY
·
2025
·
IF 7.7
Jie Yao,Hao Liu,Wei Liu,Jianxin Nie,Shi Yan,Xueyong Guo
Metal fuels are widely used in energetic materials to improve their energy release. Al Si alloy fuel is an aluminum-based alloy fuel, and its slow reaction rate limits its potential application in energy material systems. Herein, Al-Si-Mg AlSi9Mgx alloy fuel had been designed and successfully prepared by gas atomization to achieve excellent reactivity characteristics. The reaction characteristics of the fuel were systematically measured by thermal analysis (TG-DSC), bomb calorimeter, volumetric explosion vessel system and laser ignition measurement. Due to the addition of highly active magnesium, the activation energy of alloy fuel was reduced, and the combustion efficiency was increased to more than 99 %, and the ignition delay time was reduced by 6.7 ms and 33.6 ms respectively. Combustion of potassium perchlorate (KP) mixtures shows that AlSi9Mgx alloy fuels had a faster flame propagation rate, 22.814 mm/s and 42.543 mm/s. The superior reaction properties of AlSi9Mgx alloy fuel are due to the presence of internal solid solution Mg or low melting point alloy compound. This work and design provide a reliable method for optimizing the energy output of alloy fuels.
研究领域:
材料科学
·
能源工程
·
冶金学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
Science China-Chemistry
·
2024
·Vol. 67
·期 7
·2282-2291
·
IF 10.4
Jiao Meichen,Jia Chunmin,Xu Hao,Wu Peng,Zhang Xian-Ming
Ge-containing Lewis acidic zeolites are typically synthesized using a conventional hydrothermal strategy from amorphous silica sources, through a long time- and energy-consuming approach limiting their wide applications. This study reports a rapid synthesis strategy for a series of IWV aluminogermanosilicate zeolites ( T- x -Al ) with a wide range of Si/Ge molar ratios (5–15) by interzeolite transformation of dealuminated FAU (DA-FAU). Notably, Ge-rich IWV could be obtained with crystallization time as short as one day by the equimolecular Si/Ge ratio gel. The effect of synthetic parameters was investigated and the obtained T- x -Al samples were characterized by XRD, SEM, EDS, ICP, 29 Si and 27 Al MAS NMR, FTIR, and N 2 physisorption analyses. Compared with a previously reported IWV germanosilicate (H-3), T- x -Al displayed a better catalytic activity in Baeyer-Villiger (BV) oxidation, attributed to the presence of the active framework Ge sites with the assistance of the extra-framework Al species. The cyclic catalysis tests revealed that the presence of framework Al species contributed to the stability of the T- x -Al . Specifically, T- x -Al , with 14-membered ring (MR) supercages, outperformed the typical 12-MR Sn-beta catalyst in the BV oxidation of large ketone-like 2-admantanone, indicating a promising potential application in the macromolecular catalytic process.
研究领域:
材料科学
·
催化化学
✓ 已验证
产品关联
DOI
高影响因子
Materials Today Communications
·
2025
·
IF 4.5
Zefeng Guo,Jianhua Zhang,Yongke Yan,Guoyu Zhang,Dongdong Liu,Zhipeng Lei,Yuanyuan Li,Lu Li
Achieving both low dielectric loss (tan δ ) and high temperature stability of ceramic capacitors can greatly broaden their potential application. In this study, the effects of Mg and Al co-substitution on the microstructure and dielectric properties of CCTO-based ceramics were investigated in CaCu 3- x Mg x Ti 4- x Al x O 12 ( x = 0, 0.025, 0.050, and 0.075) ceramics prepared by a sol-gel method. XRD analysis shows that the primary crystalline phase of CCTO is formed in all samples, indicating that Mg 2 + and Al 3+ have entered the lattice. SEM results reveal the co-substitution of Mg and Al inhibits the grain growth, leading to an increase in grain boundary density. All co-substituted samples exhibited low tan δ and excellent temperature stability. Notably, CaCu 2.95 Mg 0.05 Ti 3.95 Al 0.05 O 12 ceramics exhibited an extremely low tan δ of 0.007 (at 10 3 Hz) and its dielectric constant maintained excellent stability over a broad temperature spectrum (−125 to 150 °C), meeting the commercial standards for X8P capacitors. The reduction of tan δ is mainly attributed to the inhibition of grain growth in Mg and Al co-substituted samples, which increases grain boundary density and subsequently suppresses the mobility of oxygen vacancies, leading to an increase in grain boundary resistance. Furthermore, the improvement in temperature stability is ascribed to the reduction in the content of oxygen vacancies and the suppression of electron transitions between Ti 4+ and Ti 3+ as well as Cu 2+ and Cu + in Mg and Al co-substituted samples, resulting in an increase in grain boundary activation energy. These novel findings are hoping to contribute to not only the fabrication of new CCTO-based ceramics with extremely low tanδ and excellent temperature stability but also the application of CCTO-based ceramics at a very broad temperature range in electronic devices, new energy vehicles, aerospace, and polar scientific research equipment.
研究领域:
材料科学
·
电子工程
✓ 已验证
产品关联
DOI
高影响因子
APPLIED CATALYSIS A-GENERAL
·
2015
·
IF 3.942
Jian He,Hu Li,Ye-Min Lu,Yan-Xiu Liu,Zhi-Bing Wu,De-Yu Hu,Song Yang
A series of Al–Zr mixed oxides with different molar ratios were prepared by co-precipitation method and utilized to catalyze conversion of ethyl levulinate (EL) to γ -valerolactone (GVL). Those as-prepared catalysts were characterized by XRD, SEM, N 2 adsorption–desorption, XPS, TG, NH 3 -TPD, CO 2 -TPD and pyridine-IR. The introduction of Al into ZrO 2 was demonstrated to enlarge surface areas, as well as increase the number of acid and base sites that were catalytically active for transfer hydrogenation. Effects of Al–Zr molar ratio, calcination temperature, reaction temperature and time, catalyst dosage, and alcohols used as hydrogen donors on the catalytic performance were investigated. A high GVL yield of 83.2% at EL conversion of 95.5% could be achieved at 220 °C in 4 h over Al 7 Zr 3 -300 using 2-propanol as hydrogen donor and solvent. Poisoning experiments verified that acid–base sites played a synergic role in producing GVL from EL. Moreover, the Al–Zr mixed oxide catalyst was able to be reused for several times with a slight loss in its catalytic activity.
研究领域:
催化化学
·
可再生化学
✓ 已验证
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2024
·
IF 5.8
Pei Yang,Shuang Wang,Huihui Liu,Linghui Meng,Yongping Bai,Jinmei He
The development of multifunctional Metastable intermixed composites (MICs) is a highly coveted objective in this field. Inspired by trees, its excellent ability to grasp soil plays an important role in energy conversion. Here, leaf-like PVDF/Al@CNTs (PDC) colloids with an energy conduction network of CNTs were prepared by strong shearing and precipitation in poor solvent. This trinity system achieved synchronous super-hydrophobicity, high safety, and excellent combustion performance. The synergistic effect of CNTs, micro-clusters of PDC and β-PVDF greatly increased the water contact angle (WAC) of the samples, achieving a WAC of 140° when CNTs were added at 3 wt%. The high conductivity and unique CNTs network enable PDC's security and electromagnetic shielding of PDC. Importantly, the sensitivity of the laser ignition and the ignition delay time were tuned. The reaction process of PDC was characterized by DSC-TG-MS, and the main reaction temperature decreases with the addition of CNTs. Moreover, PDC-1 exhibits the highest ignition pressure, energy release, and combustion rate. The combustion process is characterized by simplified simulations, which verify the important role of the unique network of CNTs in PDC for energy conduction during combustion. This work presents a distinctive approach for multifunctional MICs, demonstrating encouraging potential for various applications in energetic materials.
研究领域:
材料科学
·
能源工程
·
表面科学
✓ 已验证
产品关联
DOI
高影响因子
ACS Applied Materials & Interfaces
·
2024
·
IF 8.3
Chengzuo Gong,Gaoxu Han,Jialin Lin,Qiangfeng Zhang,Binbin Wang,Menghao Yang,Zhenghong Huang,Chunxiao Zhang,Weifeng Wei
O3-type layered oxides hold significant promise as the material for cathodes in sodium-ion batteries for their favorable electrochemical properties, while irreversible structural degradation and harmful phase transitions during cyclic operation limit the practical application of these materials. In this work, we proposed a La3+/Al3+ codoping strategy in O3-Na(Ni1/3Mn1/3Fe1/3)O2 cathode materials and found that batteries with the Na (Ni1/3Mn1/3Fe1/3)0.998La0.001Al0.001O2 (NFM-La/Al) cathodes exhibited not only promoted capacity from 135.80 to 170.42 mAh g–1 at 0.2 C but also significantly enhanced cycling stability, with a 10% improvement in capacity retention compared with NFM cathodes after 300 cycles. Particularly, their rate performance was significantly improved as well. XRD and XPS tests indicated that La could expand the c-axis of NFM due to its larger ionic radius and thus significantly increased Na+ ion diffusion efficiency, and in addition, Al doping could effectively increase the content of Ni2+ and Mn4+ and thus greatly alleviated the negative Jahn–Teller effect caused by Mn3+. Moreover, consistent with XRD analyses, DFT calculations further substantiated the effectiveness of the La/Al codoping strategy by demonstrating the detailed atom substitution mechanism in the NFM crystal lattice. The boosted structure stability and Na+ diffusion kinetics may enhance the potential for practical applications of O3-type oxide cathodes.
研究领域:
材料科学
·
电化学
·
能源存储
✓ 已验证
DOI
高影响因子
FUEL
·
2023
·
IF 7.4
Deshi Yang,Jianpeng Huang,Zhipeng Hu,Yuanyuan Miao,Fengqiang Wang,Zhijun Zhang,Yanjun Xie,Shouxin Liu,Qingwen Wang,Charles U. Pittman
Lignin is the most abundant aromatic biopolymer. Thus, preparation of BTX (benzene, toluene and xylenes) by catalytic fast pyrolysis (CFP) of lignin is attractive. Ni-Al mixed metal oxide (MMO) catalysts, derived from pyrolyzing Ni-Al layered double hydroxides (LDH), were prepared for the catalytic fast pyrolysis of lignin. The effects of catalyst Ni/Al ratio, catalyst dosage and pyrolysis temperature on the liquid products were investigated by Py-GC/MS. The Ni 3 Al 3 -MMO produced the best liquid product distribution from lignin at 700 ℃. The selectivity of Ni 3 Al 3 -MMO for aliphatic hydrocarbons and monocyclic aromatic hydrocarbons (MAHs) was 18.0% and 78.2%, respectively. The selectivity to polyaromatic hydrocarbons (PAHs) was 3.8%. No phenols and phenolic derivatives were produced. This is related to the mesoporous catalytic structure (pore size of 14.37 nm), large external surface area (134.74 m 2 /g) and strong acidity (4.92 mmol NH3 /g) of Ni 3 Al 3 -MMO. In addition, a mechanistic study was performed with the lignin model compound (guaiacol) showing that Ni 3 Al 3 -MMO exhibits strong deoxygenation activity for aromatic C–O bond cleavage of lignin.
研究领域:
化学工程
·
生物质能转化
✓ 已验证
产品关联
DOI
高影响因子
POWDER METALLURGY AND METAL CERAMICS
·
2021
·Vol. 59
·期 11
·651-660
·
IF 0.511
Zhangjun Bai,Yuhong Chen,Lu Li,Jiaxin Li,Yuewei Cheng
In this study, Ta–W–Ti–Al multialloys were prepared by spark plasma sintering (SPS) as a new powder metallurgy technology based on discharge activation and thermoplastic deformation process. The oxidation behavior of the as-obtained sintered alloys were investigated under 1000 and 1200°C in air atmosphere. Microstructures and phase compositions of alloys and oxides were analyzed using various analytical methods, such as X-ray diffraction (XRD), scanning electron microscopy (SEM) equipped with energy dispersive spectroscopy (EDS), and backscatter electron microscopy (BSE). The sintered samples possessed relative densities reaching up to 98% with achievable densification. The densities of all specimens with high Ti contents exceeded 100%, suggesting the great impact of Ti addition on liquid-phase precipitation. Intermetallic compounds were formed in Ta–W–Al alloys, and samples with high Ti contents displayed grain boundary phases rich in titanium and oxygen. The addition of Ti and Al effectively improved the oxidation resistance of the resulting alloys. A protective alumina layer was formed after oxidation at 1000°C that made oxidation kinetics of the alloys obeying pseudo-parabolic laws. At the oxidation temperature of 1200°C, Al 2 O 3 reacted with Ta 2 O 5 to form the AlTaO 4 alloy with reduced protective effect. The mass gain in the alloys after oxidation at 1200°C for 4 h was about 7 times higher compared to processing at 1000°C.
研究领域:
材料科学
·
冶金工程
✓ 已验证
DOI
高影响因子
Russian Journal of Physical Chemistry A
·
2023
·Vol. 97
·期 13
·2966-2975
·
IF 0.7
Liu Kun,Zhu TianHan,Li Feng,Wang Jing,Song Hua
A series of Ni/SiO 2 –Al- x catalysts ( x is the initial mass ratio of SiO 2 to Al(NO 3 ) 3 ) with different aluminum contents was prepared by impregnation method using nickel nitrate as the Ni source. The prepared Ni/SiO 2 –Al- x catalysts were characterized by XRD, BET, TPR, TEM, XPS, NH 3 -TPD, and Py-FTIR methods. Taking m -cresol as a model compound, the effects of aluminum content and reaction conditions on the HDO performance were investigated. Results showed that addition of appropriate amount of aluminum can generate acid sites and improve the metal Ni dispersion by increasing the surface area of catalyst. Furthermore, the selectivity to deoxygenated methyl-cyclohexane product over aluminum modified Ni/SiO 2 –Al- x catalysts increased significantly as compared to that of Ni/SiO 2 , which confirmed the importance of aluminum addition on the dehydration of 3-methyl-cyclohexanol to methyl-cyclohexane. Among the prepared Ni/SiO 2 –Al- x catalysts, the Ni/SiO 2 –Al-5 catalyst exhibits the best HDO performance. A 100% m -cresol conversion with the selectivity to MCH of 100% was achieved under the conditions of T = 250°C, p = 2 MPa, t = 75 min with catalyst (mg)/ m -cresol solution = 2.
研究领域:
催化化学
·
能源化学
·
材料化学
·
工业催化
·
绿色化学
✓ 已验证
DOI
高影响因子
ACS Applied Nano Materials
·
2021
·
IF 5.097
Muhammad Amin Padhiar,Minqiang Wang,Yongqiang Ji,Zhi Yang,Yun Zhou,Hengwei Qiu,Hao Wang,Azaz Ali Shah,Arshad Saleem Bhatti
Perovskite nanocrystals (PNCs) are ideal for optical devices due to their adjustable emission band and high photoluminescence. However, blue light-emitting perovskite nanocrystals (PNCs) exhibit poor performance compared to their green and red-emitting PNC counterparts. Herein, we introduce a simple strategy for increasing the stability of blue light-emitting CsPb (Br/Cl)3 PNCs passivated with an Al-doped CdSe layer. This simple strategy successfully achieves highly stable PNCs with photoluminescence (PL) emission ranging from 454 to 460 nm with a full width at half-maximum (FWHM) ranging from 18 to 22 nm; changes in bandgaps are also observed, and the corresponding PLQY values show a significant change after CdSe/Al modification. In addition, CsPb (Br/Cl)3 PNCs with a CdSe layer doped with Al formed on the surface show remarkable stability under ambient conditions, including thermal exposure, water resistance, and ultraviolet (UV) irradiation. A light-emitting diode (LED) device was constructed to demonstrate the feasibility of the approach by combining the optimal CsPb(Br/Cl)3/CdSe/Al PNCs with an existing commercial 365 nm UV chip, resulting in bright blue light emission with CIE color coordinates of (0.16, 0.09). All of the findings suggest that doped CsPb (Br/Cl)3/CdSe/Al PNCs have the potential to be used as color converters in liquid crystal displays (LCDs).
研究领域:
材料科学
·
光学工程
✓ 已验证
DOI
高影响因子
Journal of Environmental Chemical Engineering
·
2025
·
IF 7.2
Yiwei Sun,Xiaoli Wei,Fangcao Liu,Bing Liu,Jiaming Zhao,Yubao Bi,Wenfeng Han
Developing effective techniques to produce and stabilize highly active metastable F-Al-O species in HFCs dehydrofluorination system without being over-fluorinated to Al-F is a major challenge. Herein, we report a new strategy for the formation and stabilization of metastable species. Using NaH 2 PO 4 as a P source, phosphoric acid groups are modified to the surface of Al 2 O 3 leading to the fabrication of AlPO 4 /Al 2 O 3 interface. P and Al 2 O 3 bond to form Al-O-P structure at the interface and stabilize F-Al-O in the dehydrofluorination system. Further studies show that AlPO 4 /Al 2 O 3 interface increase the oxygen vacancy content of catalyst and accelerate the conversion of HFC-152a on the catalyst surface. Meanwhile, AlPO 4 /Al 2 O 3 interface improves the surface acidity of Al 2 O 3 , endue a large number of Lewis weak acid sites, reducing the carbon accumulation of catalyst, and improving the stability of catalyst. The activity test showed that AlPO 4 /Al 2 O 3 interface shows high catalytic performance (74.2 %) and excellent stability (50 h) for 1,1-difluoroethane dehydrogenation compared with Al 2 O 3 (30 % and low stability) without P modification.
研究领域:
化学工程
·
环境科学
·
催化材料
✓ 已验证
产品关联
DOI
高影响因子
Catalysis Science & Technology
·
2014
·Vol. 4
·期 4
·1028-1037
·
IF 4.76
Haiping Li,Quanhua Deng,Jingyi Liu,Wanguo Hou,Na Du,Renjie Zhang,Xutang Tao
Bi2MoO6/Zn–Al layered double hydroxide (LDH) hierarchical heterostructures assembled from Bi2MoO6 hierarchical hollow spheres and Zn–Al LDH nanosheets were synthesized by a low-temperature hydrothermal method. X-ray diffraction, Fourier transform-infrared spectroscopy, thermogravimetric analysis and X-ray photoelectron spectroscopy (XPS) confirmed the formation of the Bi2MoO6/Zn–Al LDH composites. Morphologies were characterized by scanning electron microscopy and transmission electron microscopy (TEM). XPS and high resolution TEM indicated the formation of a Bi2MoO6/Zn–Al LDH heterojunction. Increasing the LDH content from 0 to 27.0 wt.% caused the Brunauer–Emmett–Teller (BET) specific surface area of the composites to gradually increase. The photocatalytic degradation activity for Rhodamine B (RhB) under visible light irradiation exhibited a large enhancement, followed by a decrease, with increasing LDH content. The Bi2MoO6/Zn–Al LDH heterostructure composite with LDH content of 5.5 wt.% showed the highest photocatalytic activity and degraded 99% of RhB in 80 min, while Bi2MoO6 degraded less than 50%. The average photocatalytic efficiency is enhanced by more than 100%. The enhanced photocatalytic activity of the Bi2MoO6/Zn–Al LDH heterostructure photocatalyst was mainly attributed to the efficient separation of photoinduced electrons and holes. Superoxide radicals and holes were the major active species. The Bi2MoO6/Zn–Al LDH heterostructure photocatalyst exhibited excellent stability and reusability. A detailed mechanism for its enhanced photocatalytic activity was discussed in this study. This work provides an effective way to fabricate a series of Bi-based and LDH-containing heterostructure photocatalysts.
研究领域:
材料科学
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子