APPLIED CATALYSIS B-ENVIRONMENTAL
·
2024
·
IF 20.2
Han Xu,Qin Yang,Mingjiao Tian,Yaruo Zhao,Dong Guo,Zeyu Jiang,Yanfei Jian,Yadi Wang,Fan Dang,Chunli Ai,Jialei Wan,Reem Albilali,Chi He
Revealing the mechanism behind active oxygen species in chlorinated volatile organic compounds (CVOC) destruction is crucial but challenging. Herein, we designed a chromium-substituted titanium bimetal catalyst with strengthened element interaction, exhibiting remarkable ability to activate oxygen and destroy intermediates. Encapsulated chromium species triple the electron transfer speed (Cr → TiO 2 ), converting 90 % of vinyl chloride at 244 °C. The constructed Cr 6 + −O−Ti 3+ structure distorts TiO 2 lattice, generating defects that promote oxygen species activation. In-situ technologies and DFT calculations demonstrate that vinyl chloride adsorbed at Cr 6+ =O sites is oxidized by lattice oxygen, forming C O species, while surface oxygen activates in a cyclic process, promoting the *CH 2 CH to *CH 2 CHO and CH 2 CO. The constructed Cr-O-Ti structure breaks the rate-limiting step of *CH 2 CHO to CH 2 CO process, accelerating the formation of *CH 3 CO and further promoting the deep oxidation process (*CHO + *CO). This work presents new findings towards CVOC highly efficient purification, showcasing significant application potential.
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Materials Research Letters
·
2024
·
IF 8.6
Xiaoqi Mao,Lianwen Wang,Guodong Sun,Xuezhe Zhang,Yongqing Fu,Longlong Dong
Breaking trade-off barriers of strength-ductility in Ti alloys and their composites has been a key challenge for their engineering applications. Herein, we developed a new strategy of introducing β-Ti ductile zones in heterostructured (Cu@CNTs/TC4)+TC18 composites, which were synthesized using two-stepped ball milling, spark plasma sintering and hot rolling processes. Such composites are composed of TC18-coarse grain zones (CGZ) and (TiC+α'')-reinforced TC4-fine grain zones (FGZ). They achieve an exceptional high strength and high ductility, which are superior to those of TC4 alloys and homogeneous Cu@CNTs/TC4 composites. Heterogeneous interfacial microstructures of TC4-FGZ/TC18-CGZ play an important role in strengthening and toughening effects. The grain-coordinated deformation between TC18-CG and TC4-FG is also the key reason for achieving an exceptional ductility.
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JOURNAL OF MOLECULAR LIQUIDS
·
2025
·
IF 5.2
Xiupei Yang,Hanyu Yang,Die Deng,Yujie Kang,Yuxiu Fan,Ya Wang
Copper (Cu) nanoparticles have been widely used as catalysts for colorimetric assays. The challenge in developing Cu nanoparticles is to design nanomaterials with high catalytic activity and stability. Herein, a series of NH 2 -MIL-125(Ti)@Cu (Ti-MOF@Cu) composites with enzyme activity were obtained by in situ growth of different proportions of copper on titanium-based metal organic frameworks (Ti-MOFs), among which [email protected] showed the highest enzyme activity. Electron transfer at the interface of Ti-MOF and Cu promoted the decomposition of hydrogen peroxide (H 2 O 2 ) to generate active species under near-neutral conditions, thereby oxidizing colorless TMB to blue oxidized TMB (ox-TMB). On this basis, a sulfide ion (S 2− ) detection method based on a [email protected] colorimetric sensor was constructed, in which the limit of detection (LOD) was 0.16 μM in the linear range of 0.5–30 μM. Furthermore, [email protected] was successfully used for detecting S 2− in water samples. The successful synthesis of Ti-MOF@Cu provides new insights for further study of the enzyme-like activity of copper-based materials, and the constructed facile and sensitive sensor system has broad application prospects.
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CHEMICAL ENGINEERING SCIENCE
·
2024
·
IF 4.1
Yang Xu,Dong Lin,Ze Zong,Qiuming He,Zhe Ma,Xuliang Deng,De Chen,Chaohe Yang,Xiang Feng
Demetalation-metalation method has gained prominence for its higher metal loading, efficiency and shortened synthetic period, particularly in the incorporation of metal atoms with large radii into zeolite framework in recent years. An ammonia-regulated approach has been developed for selectively evolved deep-substituted Ti precursors in dealuminized beta zeolites, which enables a controlled promotion of metalation of Ti atoms. Additionally, this ammonia-regulated approach could also enhance 1-hexene kinetic adsorption by constructing mesopores, which is demonstrated by the lower reaction order of 1-hexene. The synthesized ammonia-regulated N-Ti-beta exhibits rich framework Ti species and a high specific surface area, leading to significantly improved 1-hexene epoxidation performance (conversion of 61%, selectivity of 98%, and a high H 2 O 2 utilization efficiency of 93%). This study not only provides a new strategy to dynamically regulate evolution of Ti precursors by ammonia but also holds promise for advancing related industrial processes in demetalation-metalation methods.
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RSC Advances
·
2024
·Vol. 14
·期 8
·5142-5148
·
IF 3.9
Chunhong Jin,Jingchao Liu,Yilin Yin,Zenghe Li
In wastewater containing heavy metals, Cr(VI) is a potentially toxic metal, mainly derived from production and processing processes such as textile printing, dyeing, ore mining, battery applications, metal cleaning and electroplating. WO3 is widely used in photocatalytic degradation and reduction, and its utilization rate of visible light is high. However, the rapid recombination of photogenerated electron–hole pairs of WO3 limits its use. In this work, the composite material (WxMy) of WO3 and MIL-125 (Ti) was prepared by the ball milling method, and the catalyst was used to photocatalytically reduce Cr(VI). After using W90M10 as a photocatalyst for 50 min, the reduction rate of Cr(VI) can reach 99.2%, and the reduction rate is 2.3 times that of WO3. After 5 cycles of use, the reduction rate can still reach 91.3%. It is mainly due to the formation of a II-type heterojunction between WO3 and MIL-125 (Ti), which promotes the separation of photogenerated electron–hole pairs, thus improving the efficiency of photocatalytic reduction of Cr(VI).
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NANOTECHNOLOGY
·
2024
·Vol. 35
·期 42
·425702
·
IF 2.9
Rui Li,Huilin Hu,Furong Xiong,Xiang Xue,Minqi Wu,Xuan Zuo,Wang Zhang,Xiangliang Pan
Efficient metal–organic frameworks (MOFs) photocatalytic bactericidal catalysts are urgently needed in water purification. Herein, a Fe-MOF (MIL-88B-NH2(V1Fe5) with promoted electron transport was achieved by vanadium (V) ions doping and V/Fe ratio optimization, showing excellent photocatalytic bactericidal activity against E. coli under visible light irradiation (99.92%). The efficient antibacterial mechanism, V as a Ti-like mediator boosting electronic transmission in MIL-88B-NH2(V1Fe5), was revealed by its band structure, transient photocurrent, electrochemical impedance spectroscopy, and scavenger quenching experiments. The enhancement of photocatalytic bactericidal performance of Fe-MOFs by V–ion-doping was confirmed by two other Fe-MOFs, MIL-53-NH2(V1Fe5) and MIL-101-NH2(V1Fe5), with the same metal ions and ligands, both of which have higher performance than the corresponding undoped MOFs. Among them, MIL-88B-NH2(V1Fe5) exhibits the highest photocatalytic bactericidal activity due to its suitable metal clusters ([M(μ3-O)] cluster) and topological structure (three-dimensional rhomboid network structure). This work demonstrated the amplification effect of V ion doping on electron transport in Fe-MOFs photocatalysts.
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CATALYSIS LETTERS
·
2025
·Vol. 155
·期 2
·1-18
·
IF 2.4
Xu Lingling,Pan Xiaomei,Gao Lijing,Wei Ruiping,Li Jihang,Wen Xiu,Li Yuanzhuang,Xiao Guomin
UiO–66–NH 2 (Ti/Zr) modified by Ti metal oxide (TiO 2 ) was used to catalyze the hydrolysis of cellulose to prepare 5-HMF. Under the optimal reaction conditions of H 2 O(NaCl)/THF(1/4 mL), 190 °C, 2 h and 50 mg UNT-3(Ti/Zr) (TiO 2 and UiO–66–NH 2 with mass of 1.5 and 0.1 g, respectively), the yield of 5-hydroxymethylfurfural reached 59.88%. UiO–66–NH 2 (Ti/Zr) nanocomposites with different mass ratios were successfully prepared by simple solvent evaporation method. SEM and TEM have shown that the modified UiO–66–NH 2 (Ti/Zr) are wrapped into sphere by TiO 2 densely attached to the surface of UiO–66–NH 2 , which provides favorable conditions for the uniform dispersion of TiO 2 and coordination of the Lewis acidic site of UiO–66–NH 2 . NH 3 –TPD results confirmed the existence of super-strong, strong, middle and weak acid sites in UiO–66–NH 2 (Ti/Zr), and Py-FTIR confirmed the existence of Brønsted and Lewis acids. After four cycles, the yield of 5-HMF and FUR decreased slightly from 59.88 to 51.89% and 9.11 to 7.66%, respectively, and the yield of 5-HMF could still remain above 50%. The results showed that the modified composite treatment of TiO 2 with rich Lewis acid/base and UiO–66–NH 2 could provide a certain idea for the extensive application of biomass research in the future. Graphic
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2024
·
IF 5.8
Zi-Xuan Jin,Ting-Ting Ma,Yue-Ying Liu,Zhi-Qian Jia,Hong-Wei Tan,Wen-Juan Peng
Ti-based Li-ion sieve (H 2 TiO 3 , HTO), is attractive for adsorbing lithium from salt lakes. Nevertheless, the titanium dissolution and limited adsorption capacity affect the cycling stability and adsorption performance. In this work, an atom engineering technique was employed by doping tungsten (W) into layered HTO via a hydrothermal method. Through experiments and theoretical simulation, it was demonstrated that the doped W in HTO results in expanded interplanar spacing, increased surface adsorption energy, and excellent adsorption performance. The optimized HTO-W exhibits an Ti dissolution rate of 0.73 % (in 2 mol L −1 HCl for 12 h, 5.6 % that of pristine HTO) and adsorption capacity of 43.01 mg g −1 (in 425 mg L −1 LiCl solution at 30 °C, 1.4 times that of undoped HTO). Furthermore, the HTO-W reaches adsorption equilibrium in about 3 h with exceptional selectivity and stability. This work demonstrates an effective enhancement of lithium adsorption by W doping, providing new avenues for developing lithium adsorbents with high performance.
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CERAMICS INTERNATIONAL
·
2025
·
IF 5.6
Liangcai Du,Qianqian Kong,Lichao Gong,Huachen Liu,Song Huang,Yunqi Xie,Zhenhua Yao
High entropy alloys (HEAs) exhibit distinctive core effects and excellent properties, presenting promising prospects for various applications, particularly as potential cermet adhesives. (Ti,W)C-HEA cermets were synthesized using vacuum sintering, employing mechanically alloyed CoCrFeNiTi HEA powder as a binder. The microstructure and mechanical properties of the produced cermets were systematically analyzed, with a particular focus on the effect of the HEA binder on the mechanical properties of the cermets. The findings indicated a decreasing trend in relative density, Rockwell hardness, and transverse rupture strength (TRS) of the cermets. Notably, the CM1 group ((Ti,W)C-30 wt% Co 20 Cr 20 Fe 20 Ni 35 Ti 5 ) demonstrated the most favorable overall properties, with values of 97.0 % for relative density, 83.2 HRA for Rockwell hardness, and 776.6 MPa for TRS. The phase transformation of HEAs at elevated temperatures was meticulously investigated using differential scanning calorimetry (DSC) and heat treatment. Combined with X-ray diffraction (XRD), the phase transformation of Co 20 Cr 20 Fe 20 Ni 25 Ti 15 and Co 20 Cr 20 Fe 20 Ni 15 Ti 25 , heat treated at increasing temperatures, is as follows: FCC + BCC (milled) → FCC + σ (700°C–1100 °C) → FCC (bulk).
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2017
·
IF 3.133
Jing Lin,Zhanyi Cao,Lianshan Sun,Fei Liang,Limin Wang
Ti 1.4 V 0.6 Ni + x LiAlH 4 ( x = 0.5, 1, 1.5, 2, 2.5, wt.%) composites were prepared by ball-milling, and the effects of LiAlH 4 content on structure and electrochemical properties of the composites were investigated systematically. The addition of LiAlH 4 to the Ti 1.4 V 0.6 Ni alloy significantly affected the morphology and size of the composite particles . The electrochemical cycling stability and rate dischargeability of the composite electrodes benefitted from adding some LiAlH 4 ( x = 1), which however deteriorated when the LiAlH 4 content increased further. The positive effect of LiAlH 4 on the electrochemical performance of the studied alloy was caused by suppression of the dissolution of active components of the Ti 1.4 V 0.6 Ni hydrogen storage alloy.
研究领域:
材料科学
·
金属功能材料
·
能源存储
·
电化学
·
氢能技术
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Small
·
2025
·
IF 12.1
Zhengyang Li,Yuting Chen,Zhiyuan Guo,Tong Wang,Qi Fan,Yuhang Zhuang,Chenying Li,Mei Yang,Teng Xu,Yanchen Liu,Zhiyuan Li,Qin Sun,Xiaohui Zhu,Hui Xia
Manganese-based oxide cathodes for sodium-ion batteries face irreversible degradation from Mn 3+ Jahn–Teller distortion and Mn 2+ dissolution, compounded by cyclic strain during (de)sodiation. To address this, a P2-K 0.7 Mn 0.8 Ni 0.1 Ti 0.1 O 2 (KMNT) cathode via dual-regulation is developed: K + pillars expand alkali - metal layers enabling fast Na⁺ diffusion, while Ni/Ti co-doping compresses transition-metal layers to suppress Mn migration and Jahn–Teller effect. Besides, the K + pillars in discharged KMNT enhance Mn─O interactions via electrostatic effects, elevating Mn redox potentials and enabling a high average discharge voltage of ≈2.6 V (vs. Na + /Na). Even at a low potential cut-off of 1.5 V, the KMNT cathode demonstrates a reversible specific capacity of 124 mAh g −1 at 1 C with 98% capacity retention after 200 cycles and retains 83% after 900 cycles at a large current density of 10 C, significantly outperforming conventional Mn-based cathodes. Electrochemical and operando tests confirm the dynamic K + /Na + exchange mechanism and absence of Mn 2+ formation, establishing a new paradigm for stable Mn-rich cathodes.
研究领域:
材料科学
·
电化学
·
储能
·
电池技术
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高影响因子
Journal of Water Process Engineering
·
2025
·
IF 6.7
Min Zhang,Shuhuan Yin,Jia Wen,Bin Zheng,Shaohua Lin,Haixia Wu
With the increasing severity of microplastic (MPs) pollution in aquatic environments, the process of removing MPs from water environments by electrocoagulation (EC) technology has attracted widespread attention. In this study, EC using a dimensionally stable anode (DSA)-coated Ti electrode (RuO₂-IrO₂/Ti) under pulsed current was employed to treat wastewater containing polystyrene (PS) MPs. The effects of factors such as electrolyte concentration, initial solution pH, current density, pulse frequency, and pulse duty cycle on the PS removal efficiency were investigated. The results showed that the maximum PS removal of 94.2 % was achieved with an energy consumption of 5.5 kWh/g. The removal mechanism of PS was elucidated through analyses including scanning electron microscopy-energy dispersive spectroscopy, X-ray photoelectron spectroscopy of electrode, X-ray diffraction, fourier transform infrared, and zeta potential measurement of the flocs. Finally, the article conducts an economic analysis of this technology and provides an outlook on its application prospects. This study confirms that the EC technology using RuO₂-IrO₂/Ti can remove MPs from wastewater effectively, which may provide new insights for the development of MPs removal technologies.
研究领域:
环境科学
·
水处理技术
·
电化学工程
·
环境功能材料
·
污染控制化学
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