APPLIED ORGANOMETALLIC CHEMISTRY
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2021
·Vol. 35
·期 10
·e6342
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IF 4.105
Yue Dai,Tangtong Ju,Hailong Tang,Meiling Wang,Min Wang,Yongqing Ma,Ganhong Zheng
A novel composite of N-doped TiO 2 -quantum dots tightly anchored on graphene (denoted as N-doped TiO 2 -QDs@GP) with superior interfacial contact via C–Ti bond was synthesized via the simple one-pot vapor-thermal method. The as-obtained N-doped TiO 2 -QDs@GP includes TiO 2 QDs with an average size of 3.28 nm uniformly distributed on the surface of GP. The large specific area and superior interfacial contact via C–Ti bond ensured its potential photocatalytic application. Except for the effective interfacial charge transfer achieved via C–Ti chemical bond between TiO 2 QDs and GP, its enhanced visible light absorption and larger oxygen vacancy ratio also make contributions. Electron spin resonance spectra (ESR) were used to study the photocatalytic mechanism, which proved the participation of both superoxide radical (·O 2 − ) and hydroxyl radical (·OH) in the photocatalytic reactions. This work provides a promising one-pot method for constructing intimately contacted N-doped TiO 2 /GP composite with superior interfacial contact via C–Ti bond and excellent photocatalytic activities.
研究领域:
材料科学
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纳米技术
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光催化
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复合材料
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环境化学
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CERAMICS INTERNATIONAL
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2022
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IF 5.532
Kai Lv,Yong Zhu,Lei Wang,Zhang Chen,Zongtao Zhang,Yanfeng Gao
To reduce carcinogenic cobalt content in pigments, a series of near-infrared reflective pigments based on CaAl 12-x-y Co x Ti y O 19 (x = 0–0.5 and y = 0-(x+0.3)) were prepared via solid state reactions. Although the cobalt content in the pigment CaAl 11.7 Co 0.1 Ti 0.2 O 19 is only 0.87% by mass, the resulting pigment still has excellent color properties (64.89, 3.88, −40.30) and near-infrared reflectance (∼70%). The structural information of the obtained pigments were analyzed by XRD refinement, and the results revealed that the doping concentration of titanium relative to cobalt significantly affected the coordination structure of cobalt in hibonite, which in turn apparently influenced the optical properties of the obtained samples. The actual cooling effect of the CaAl 11.7 Co 0.1 Ti 0.2 O 19 coating was tested using a model house and the annual energy consumption was simulated by using EnergyPlus software. For a warm city (Haikou), using this CaAl 11.7 Co 0.1 Ti 0.2 O 19 coating can reduce energy consumption for cooling by 24.75%.
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Materials Advances
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2023
·Vol. 4
·期 3
·940-947
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IF 5
Xiaobing Yang,Junjie Pan,Bingcong Xing,Wenjie Lei,Yingchun Fu,Kejun Cheng
Nowadays, aflatoxin B1 (AFB1) contamination is considered as one of the most common food safety issues for humans and animals. As one of the most advanced oxidation techniques, photocatalytic degradation can break down organic contaminants into nontoxic and harmless materials efficiently. In this paper, we explored the degradation efficiency of AFB1 by ZnIn2S4. To promote the photocatalytic degradation efficiency of AFB1, ZnIn2S4 was coupled with MIL-125(Ti) and then doped with La [this hybrid is denoted as La-ZnIn2S4/MIL-125(Ti)] to effectively convert it via photocatalytic generation of superoxide radicals (˙O2− and ˙OH) and achieve much enhanced photocatalytic performance, which is demonstrated by degrading 97.6% of AFB1. According to the transient photocurrent responses, the doping of La and coupling with MIL-125(Ti) can highly improve the efficient separation of the photoinduced electron–hole pairs on ZnIn2S4, leading to the effective conversion of OH− and O2 into ˙O2− and ˙OH, respectively, during the photodegradation process. This strategy of coupling with MOFs and doping with rare earth elements provides a facile and efficient method for degrading food pollutants produced by aflatoxins.
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ACS Applied Materials & Interfaces
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2022
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IF 10.383
Jianping Yang,Zhonghao Liu,Haoran Zhou,Lei Jia,Anhua Wu,Linwen Jiang
Efficient and stable electromagnetic-wave (EMW) absorption materials have attracted great attention in the field of reducing microwave pollution. Herein, FeCoNiCuTix high-entropy alloys (HEAs) as electromagnetic-wave absorbing materials were prepared by a high-energy ball-milling method. The as-milled HEA powders presented a flaky shape with a high aspect ratio. Impedance matching was efficiently optimized by severe lattice distortion, which was caused by Ti incorporation. The introduced plentiful defects in FeCoNiCuTix HEAs provided abundant polarization sites for dielectric loss. By tuning Ti contents, FeCoNiCuTi0.2 HEAs delivered excellent EMW absorption performances. The maximal reflection loss (RLmax) values reached −47.8 dB at 10.86 GHz as thin as 2.16 mm, and the widest bandwidth was 4.76 GHz (5.97–10.73 GHz). Furthermore, the introduction of Ti enhanced corrosion resistance via increasing the charge transfer resistance of a passivated film. Those characteristics of FeCoNiCuTix HEAs made these materials a practical gigahertz-range EMW absorber. Additionally, our findings provided a facile and tunable strategy for designing EMW absorbing materials, which was aimed at lightweight, highly efficient absorption, and resistance to harsh environments.
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POLYMER
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2022
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IF 4.432
Qisong Lin,Feng Gao,Yongjun Wang,Wangyang Lu,Wenxing Chen
Antimony-free poly(ethylene terephthalate) (PET) has been synthesized through polycondensation of p -phthalic acid and ethylene glycol , and then subjected to a viscosity-increasing process by liquid-state polycondensation (LSP). For both of these processes, a novel environmentally benign ethylene glycol-soluble Ti/Mg bimetal (TM) catalyst has been used. The structure of the TM catalyst has been comprehensively characterized and its catalytic activity in the polycondensation reaction has been evaluated and compared with those of other titanium-based catalysts. The results reveal that the TM catalyst is a chelated complex with high catalytic activity for polycondensation to afford PET without significant side reactions. Indeed, the LSP process catalyzed by TM affords a PET product with high intrinsic viscosity suitable for industrial yarn production (1.08 dL/g) within 60 min, and that exhibits higher thermostability with increasing intrinsic viscosity. Finally, the kinetics of the TM-catalyzed polycondensation has been probed based on the variation of intrinsic viscosity with increasing polycondensation time.
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MATERIALS SCIENCE AND ENGINEERING A-STRUCTURAL MATERIALS PROPERTIES MICROSTRUCTURE AND PROCESSING
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2022
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IF 6.044
Tao Xiang,Peng Du,Weizong Bao,Zeyun Cai,Kun Li,Guoqiang Xie
Grain refinement is perfectly efficient for improving strength , but accompanies by a dramatic loss of ductility. Here we report a bimodal grain size structure design by inducing ultra-high strength TiZrNbTa high entropy alloy (HEA) with nanoscale grain size into pure Ti with coarse grain size to achieve the strength-strain balance by establishing bimodal grain size distribution (BGSD). Through optimizing the TiZrNbTa HEA content, the 60 wt.% TiZrNbTa/Ti titanium matrix composite (TMC) exhibits a yield strength of 1426 ± 30 MPa, ultimate compressive strength of 2133 ± 88 MPa, and an acceptable compressive strain of 22.3% ± 1.8%, respectively. The compressive yield strength of 60 wt.% TiZrNbTa/Ti TMC is 3.6-fold for c.p. Ti (393.0 ± 7.1 MPa). The unusual high strength is attributed to the nanoscale grain size provided by TiZrNbTa HEA, and the acceptable compressive strain is obtained from the co-effect of coarse grain Ti and TiZrNbTa HEA. The excellent mechanical properties of 60 wt.% TiZrNbTa/Ti TMC undoubtedly greatly increase the possibility of its application as an orthopedic implant in the biomedical field.
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MICROPOROUS AND MESOPOROUS MATERIALS
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2022
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IF 5.876
Haoyi Lin,Jiaqi Wang,Boxin Gao,Kaixuan Yang,Guojun Lv,Shixue Qi,Zhiguo Zhu,Hongying Lü
Solvent-free and low-template synthesis of zeolite materials is the future direction of zeolite production, which meets the requirements of green chemistry. Ti-Beta zeolite with opened channel systems of the 3-dimensional 12-membered ring is a promising industrial catalyst in the field of selective oxidations . Herein, nanosized Ti-Beta zeolites were successfully synthesized via interzeolite transformation of siliceous MOR zeolite using sample and commercially available tetraethylammonium hydroxide (TEAOH) as organic structure-directing agents under solvent-free and low-template-content (TEAOH/SiO 2 = 0.2) conditions within a short crystallization time. The crystallization mechanism and Ti coordinated state were thoroughly investigated by numerous characterization techniques. It was found that the hydrothermal synthesis of Ti-Beta-M zeolites obeyed a liquid crystallization mechanism, during which pre-dissolution of the silicon source MOR zeolite was a critical step in achieving successful crystallization. Ti 4+ ions mainly existed in the form of tetrahedrally coordinated states in zeolite framework. Thus Ti-Beta zeolites showed remarkable activity and reusability during the oxidative desulfurization of fuel oil. Moreover, the deactivated mechanism and regenerated method were also studied in detail. This work provides new guidance for solvent-free and low template content synthesis of metallosilicate zeolites.
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ACS Catalysis
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2022
·
IF 13.7
Weiyue Zhao,Bin Chi,Lecheng Liang,Pengfei Yang,Wei Zhang,Xin Ge,Liming Wang,Zhiming Cui,Shijun Liao
Developing advanced electrocatalysts toward the sluggish oxygen reduction reaction (ORR) kinetics is critical to fuel cells but still an enormous challenge at present. Here, we demonstrate a highly active and durable Pt-based ternary catalyst, ordered Pt3Co0.6Ti0.4 intermetallic nanoparticles (∼3 nm) supported on ZIF-8-derived mesoporous carbon (Pt3Co0.6Ti0.4/DMC). The Pt3Co0.6Ti0.4/DMC catalyst exhibits faster ORR kinetics compared to Pt3Co/DMC and commercial Pt/C with minimal activity loss (20.1%) and only 5 mV decay in half-wave potential after 20,000 potential cycles. More importantly, its improved performances have also been proven in the H2/air PEM single cell test. The theoretical calculations reveal that the substitution of Ti for Co induces a strengthened ligand effect and optimizes the surface electronic structure of Pt3Co0.6Ti0.4, resulting in the significantly enhanced ORR activity. This work provides a reliable and promising approach for the development of efficient and robust Pt-based ternary intermetallic electrocatalysts for practical fuel cell applications.
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Food Analytical Methods
·
2022
·Vol. 15
·期 10
·2830-2839
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IF 3.498
Tang Jing,Li Jie,Liu Tianna,Tang Wenjing,Li Nali,Zheng Shengbiao,Guo Jiahao,Song Changchun
Electrochemical determination of tert-butylhydroquinone (TBHQ) is vital to food safety due to negative health effects; however, bare electrode of traditional electrochemical sensors generally has a narrow linear range and low sensitivity, limiting their practical application. Accordingly, the nano-architecture fabricated with N-doped TiO 2 –carbon nano-composites (TiO 2 /NC) is prepared by the thermolysis of NH 2 functionalized MIL-125(Ti) metal–organic frameworks (NH 2 -MIL-125(Ti)). TiO 2 /NC composites are firstly developed as the electrochemical material for electrochemical determination of TBHQ. The TiO 2 /NC composites with a highly porous structure, excellent conductivity and electron transportation, and large surface area show remarkable electrochemical oxidation ability for TBHQ. Under optimal conditions, TiO 2 /NC composite-modified electrode presents a broader linear response to TBHQ concentration of 0.05–100 μM with the detection limit as low as 4 nM (S/N = 3). Finally, the sensor platform is implemented directly to determine TBHQ in edible oil for evaluation of its practical application. TiO 2 /NC composites sensor fabricated perform larger linear range with high sensitivity and anti-interference properties, which can be used as a potential for electrochemical determination of TBHQ.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2022
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IF 5.518
Ming Xiao,Ruixue Li,Jinglin Yin,Junhui Yang,Xinyu Hu,Hongbo Xiao,Wenlei Wang,Ting Yang
The treatment of arsenite pollution in water has always been concerned. Oxidation of high toxic As(III) to relatively low toxic As(V) by efficient photocatalytic oxidation technology is a research hotspot. This paper is focused on the active photocatalyst of TiO 2 @Fe 3 O 4 composites synthesized by a simple hydrothermal method for the efficient photocatalytic oxidation of As(Ⅲ). The successful construction of Ti–O–Fe interface bonds between TiO 2 and Fe 3 O 4 significantly promoted the transfer efficiency of photo-generated carriers, and further rapidly improved the photocatalytic oxidation efficiency of As(Ⅲ). The application results showed that the constructed TiO 2 @Fe 3 O 4 photocatalyst with 0.10 g Fe 3 O 4 (TF-0.10) could complete the transformation from As(Ⅲ) (10,000 μg/L) to As(Ⅴ) within 4 min with a high oxidation ratio of 100% and maintained the good properties with unchanged crystal structure after five cycles. Furthermore, the photocatalytic properties of TiO 2 @Fe 3 O 4 composites were still stable under different pH values. Electron paramagnetic resonance (EPR) consequence displayed that the superoxide radical (‧O 2 — ) and hole (h + ) were the main intermediate product in the arsenic photocatalytic oxidation system, and hydroxyl radical (‧OH) had little effect on this oxidation system. The possible mechanism of As(Ⅲ) photocatalytic conversion was further explored based on the results of the data analysis. Furthermore, this work provides a potential new idea for the practicability of efficient photocatalytic arsenic oxidation.
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JOURNAL OF APPLIED ELECTROCHEMISTRY
·
2021
·Vol. 52
·期 3
·573-581
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IF 2.8
Zhao Ruiyu,Wang Yi Mou,Li Jie,Meng Wenhua,Yang Chunli,Sun Chongxiang,Lan Xuefang
Ni, Ce, and Ta modified Ti/SnO 2 –Sb 2 O 5 –RuO 2 anodes were first prepared by thermal decomposition strategy and applied for Orange G degradation to explore the effect of Ni, Ce, and Ta modification on electrocatalytic property. The Ta modified anode showed the highest ·OH generation capability and the lowest charge transfer resistance among all samples, conducive to electrocatalytic degradation of Orange G. Besides, the Ta modified anode shows more cracks than Ni and Ce modified anodes, which is expected to create more specific surface areas and more exposed active sites for Orange G degradation. The degradation efficiency and the total organic carbon (TOC) removal rate increased in the order Ru < Ru–Ni < Ru–Ce < Ru–Ta, with Ru–Ta showing the highest degradation efficiency of 98.6% and 44.2%, much higher than 79.6% and 27.5% of Ru, respectively.
Graphical abstract
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2021
·
IF 8.128
Dingliang Dai,Jianhao Qiu,Lu Zhang,Hong Ma,Jianfeng Yao
A subtle flower-like MIL-125-NH 2 @BiOI was fabricated by a facile solvothermal method for simultaneously eliminating Cr(VI)/tetracycline mixed pollutants under visible light . The strong interaction between amino in MIL-125-NH 2 and Bi 3+ of BiOI promotes the formation of this unique inlaid structure and enables the favorable contact between MIL-125-NH 2 and BiOI, thus accelerating the transfer of charge carriers. Remarkably, MIL-125-NH 2 @BiOI displays a superior activity compared with that of two monomers for the photocatalytic reduction of Cr(VI) and degradation of tetracycline . More significantly, the photocatalytic efficiency can be further boosted in the coexistence of Cr(VI) and tetracycline , which is 1.8 and 1.6 times that of single Cr(VI) and tetracycline, respectively. The synergistic effect between Cr(VI) reduction and tetracycline oxidative degradation can further facilitate the separation of photo-induced electrons and holes, resulting in the improved efficiencies in the Cr(VI)/tetracycline coexistent environment. This work sheds light on that MOF-based photocatalysts possess huge potential for practical environmental remediation.
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