CHINESE JOURNAL OF CATALYSIS
·
2018
·
IF 3.525
Pengwei Wang,Xin Zhang,Guofeng Zhao,Ye Liu,Yong Lu
Mn 2 O 3 -Na 2 WO 4 /SiO 2 is considered as the most promising catalyst for the oxidative coupling of methane (OCM) process; however, it only has a better catalytic performance over 800 °C. To improve its low-temperature performance, an attempt has been made to modify the Mn 2 O 3 -Na 2 WO 4 /SiO 2 catalyst using TiO 2 , MgO, Ga 2 O 3 , and ZrO 2 . Among the synthesized catalysts, the TiO 2 -modified Mn 2 O 3 -Na 2 WO 4 /SiO 2 catalyst shows markedly improved low-temperature OCM performance, achieving a high CH 4 conversion of ~23% and a good C 2 -C 3 selectivity of ~73% at 700 °C (the catalyst bed temperature), along with promising stability for at least 300 h without signs of deactivation. In comparison with the unmodified Mn 2 O 3 -Na 2 WO 4 /SiO 2 catalyst, the TiO 2 modification results in significant improvement in the low-temperature activity/selectivity, whereas the MgO modification has almost no impact and the Ga 2 O 3 and ZrO 2 modifications have a negative effect. The X-ray diffraction (XRD) and Raman results reveal that the formation of a MnTiO 3 phase and a MnTiO 3 -dominated catalyst surface is crucial for the improvement of the low-temperature activity/selectivity in the OCM process.
研究领域:
化学工程
·
催化科学
✓ 已验证
DOI
高影响因子
ACS Applied Materials & Interfaces
·
2020
·
IF 8.758
Bei Hu,Fushan Geng,Chong Zhao,Bertrand Doumert,Julien Trébosc,Olivier Lafon,Chao Li,Ming Shen,Bingwen Hu
The layered Mn-based oxides (NaxMnO2), which is one of the most promising cathode families for rechargeable sodium-ion batteries, have received considerable attention because of their tunable electrochemical performances and low costs. Herein, a novel P2/O3 intergrown Li-containing Na0.8Li0.27Mn0.68Ti0.05O2 cathode material prepared by Ti-substitution into Mn-site is reported. Benefiting from the synergistic effects of the biphasic composite structure and inactive d0 element substitution, this P2/O3 electrode exhibits high initial charge/discharge capacity and excellent cycling performance. The combination of different characterization techniques including solid-state NMR, electron paramagnetic resonance, X-ray adsorption spectroscopy, and high-resolution transmission electron microscopy gives insights into the local electronic environment, the redox chemistry, and also the microstructure rigidity of these cathode materials upon cycling. On the basis of comprehensive comparison with the Ti-free P2/O3-Na0.8Li0.27Mn0.73O2, the observed improvement on the electrochemical performance is primarily attributed to the mitigation of notorious Mn3+/Mn4+ redox and the enhanced stability of the oxygen charge compensation behavior. From the viewpoint of structure evolution, Ti-substitution restrains the Li+ loss and irreversible structural degradation during cycling. This study provides an in-depth understanding of the electronic and crystal structure evolutions after inactive d0 element substitution and may shed light on the rational design of high-performance P2/O3 biphasic Mn-based layered cathodes.
研究领域:
材料科学
·
电化学
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DOI
高影响因子
KOREAN JOURNAL OF CHEMICAL ENGINEERING
·
2021
·Vol. 38
·期 2
·442-453
·
IF 3.309
Cui Yanhua,Yang Lili,Yan Yan,Wang Zengkai,Zheng Jian,Li Binrong,Feng Yonghai,Li Chunxiang,Meng Minjia
The photocatalytic efficiency of conventional blending photocatalytic membranes suffers a significant reduction due to effective photocatalyst embedded in membrane matrix. Therefore, in this study, inspired by the bioadhesive technology of polydopamine (pDA), a novel Ti doped bismuth oxyiodide (BiOI)-polydopamine (pDA)-coated cellulose acetate (CA) (Ti/BiOI-pDA/CA) photocatalytic nanocomposite membranes were successfully developed for effective removal of tetracycline (TC). The Ti/BiOI-pDA/CA nanocomposite membranes displayed very high photocatalytic activity toward TC (about 98% after 120 min) under visible light irradiation and superior photodegradation kinetics (k=0.03214 min −1 ). The removal rate of Ti/BiOI/-pDA/CA nanocomposite membranes under dynamic cyclic degradation system could be further improved, giving TC removal efficiency of 91% in 60min. Remarkably, the permeate flux, flux recovery ratio (FRR), reversible fouling (Rr), irreversible fouling (Rir) and the total fouling ratio (Rt) revealed the Ti/BiOI-pDA/CA nanocomposite membranes had excellent antifouling performance. In addition, the Ti/BiOI-pDA/CA nanocomposite membranes exhibited excellent stability and reusability. Therefore, this work gives insight into the effective removal of TC wastewater and has a great potential for new generation of high-performance photocatalytic membranes for practical wastewater treatment in the future.
研究领域:
环境科学
·
材料科学
✓ 已验证
DOI
高影响因子
MATERIALS RESEARCH BULLETIN
·
2023
·
IF 5.4
Zhiwei Li,Zhengxiang Bian,Yurong Ren,Zhihui Chen,Jiujun Xu
(1-x)(0.9Ba 1.003 Ti 0.97 Ca 0.03 O 3 –0.1(Bi 0.51 Na 0.47 ) 0.94 Ba 0.06 TiO 3 )-xNa(Nb 0.85 Ta 0.15 )O 3 ( x = 0.03–0.15) ceramics were designed and fabricated through a bidirectional optimization strategy using traditional solid reaction method. The results revealed that the introduction of Na(Nb 0.85 Ta 0.15 )O 3 increased the vacancy concentration at the A site , conducing to improved polarization and reduced grain size. The substitution at the B site disrupted the long-range ordered ferroelectric domains and generated polar nanodomains, leading to enhanced relaxation behavior. The optimum energy storage density of 3.57 J/cm 3 and efficiency of 87.5% were simultaneously achieved under the electric field of 220 kV/cm in the sample with x = 0.09. Moreover, it also exhibits extremely high-power density (∼57 MW/cm 3 ), ultrafast discharge time (∼103 ns), high discharge density (1.35 J/cm 3 ), along with excellent temperature (30‒120 °C) and frequency stability (1‒100 Hz) under the equivalent electric field of 120 kV/cm. This novel design strategy provides theoretical guidance for the development of advanced electrical energy storage devices.
研究领域:
材料科学
·
能源存储
✓ 已验证
DOI
高影响因子
NEW JOURNAL OF CHEMISTRY
·
2021
·Vol. 45
·期 14
·6543-6549
·
IF 3.591
Ziqi Zhang,Xiang Ni,Kaida Yao,Siqi Zhang,Yang Liu,Yueqiu Sun,Xiangzhi Wang,Weimin Huang,Yan Zhang
Titanium has been applied to implants over the last decades due to its excellent biocompatibility and mechanical properties. However, there are still some drawbacks for titanium and its alloys to overcome. Thus, in this study, a novel electrochemical synthesis process has been developed to fabricate TiO2 nanotube array, hydroxyapatite and rare-earth (La3+) doped ZIF-8 nanoparticle composite coating, which can enhance the antibacterial and anti-corrosion property on the premise of minimizing the biocompatibility loss of titanium implants. Compared with traditional processing methods, electrochemical machining is more time-saving, energy-saving and environment-friendly. Thus, it provides an alternative way to produce medical implants.
研究领域:
生物材料学
·
医学工程
·
电化学
✓ 已验证
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2020
·
IF 10.652
Yawen Cai,Yapeng Ma,Jinghua Feng,Mingyu Zhu,Xin Wang,Zhimin Lv,Ming Fang,Xiaoli Tan,Xiangke Wang
The efficient treatment of uranium (U) is an important and challenging issue regarding radioactive wastes management. Adsorbent with high efficacy, low-cost is urgently needed for alleviating the contamination of U-containing wastewaters. To solve these issues, we report a series of phytic acid (PA) modified Zn-Al-Ti layered mixed metal oxides (Zn-Al-Ti LMO@PAs) in this work, which shows the adsorption capacity as high as ∼1486 mg/g and could be easily obtained through a facile post-modification method. The adsorption performance of Zn-Al-Ti LMO@PAs for U(VI) are carefully estimated through batch experiments. With the aid of batch experiments and various characterization techniques, PA in Zn-Al-Ti LMO@PAs is found to make the most contribution for the chelation of U(VI), which favors for the adsorption selectivity and capability. The Zn-Al-Ti LMO@PAs are potential cost-effective adsorbents to remove the U(VI) in wastewaters.
研究领域:
环境科学
·
材料科学
✓ 已验证
DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE
·
2019
·Vol. 55
·期 2
·701-712
·
IF 3.442
Yang Wangyang,Shen Honglie,Min Huihua,Ge Jiawei
In recent years, Ti 3+ self-doped TiO 2 (B-TiO 2 ) exhibits great potential as a photocatalyst. In this work, Ti vapor-assisted annealing is first demonstrated for Ti 3+ doping and improving the visible absorption of TiO 2 . TEM results exhibit the formation of disordered layer, indicating the successful fabricating of B-TiO 2 . The absorption increase in TiO 2 caused by Ti vapor annealing reaches nearly 50% in the visible wavelength range. Benefiting from the absorption increase, the photocatalytic performance of TiO 2 after Ti vapor annealing increases by 60–70%. Surface modification of Ag onto B-TiO 2 is also carried out to further improve its optical property. Ag-modified Ti 3+ self-doped TiO 2 (B-TiO 2 @Ag) exhibits great visible photodegradation behavior to RhB. The RhB degradation rate reaches 97.76% after 60 min of visible light irradiation. Electrochemical performance tests demonstrate that as-prepared TiO 2 @Ag has lower resistance than W-TiO 2 . The results indicate that B-TiO 2 @Ag has great potential in solar photocatalytic degradation of pollutant.
研究领域:
材料科学
·
环境科学
·
化学工程
✓ 已验证
DOI
高影响因子
ENVIRONMENTAL SCIENCE & TECHNOLOGY
·
2019
·
IF 7.149
Huiling Liu,Jinglong Han,Jili Yuan,Chengbin Liu,Dong Wang,Tian Liu,Meijun Liu,Jinming Luo,Aijie Wang,John C. Crittenden
Efficient elimination of antibacterial activity of halogenated antibiotics by dehalogenation pretreatment is desired for a biochemical treatment process. In this study, crystalline cobalt phosphide nanosheet arrays on a Ti plate (C-CoP/Ti) are fabricated by a simple electrodeposition and phosphorization process. The crystalline structure greatly promotes atomic hydrogen (H*) generation. Moreover, the nanosheet arrays can provide abundant active sites and accelerate electron transfer and mass transport. As a result, the dehalogenation rate of florfenicol (FLO, an emerging organic pollutant) on C-CoP/Ti is 11.1, 2.97, and 13.6 times higher than that on amorphous CoP/Ti, Pd/Ti, and bare Ti, respectively. The C-CoP/Ti electrode achieves 97.4% dehalogenation of FLO (20 mg L–1) within 30 min at −1.2 V (vs Ag/AgCl). Nearly 100% of Cl and 20% of F are broken away within 120 min, showing the highest electrocatalytic defluorination efficiency reported so far. Both experimental results and theoretical calculations reveal that the dehalogenation of FLO on C-CoP/Ti is synergistically accomplished via direct reduction of electron transfer and indirect reduction of H*. This study develops a highly efficient non-noble metal electrode material for dehalogenation of halogenated organic compounds.
研究领域:
环境科学
·
材料科学
·
化学
✓ 已验证
DOI
PubMed
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2026
·
IF 6.7
Hao Li,Yao Tang,Zhicai Zhang,Chao Wang,Zhiqiang Hou,Yikan Yang,Jiao Yang,Haikuo Wang
Three-dimensional network-structured titanium matrix composites are promising for elevated-temperature applications, but their performance is often limited by grain coarsening and interfacial instability. In this work, Ti-6Al-4V matrix composites reinforced with in-situ TiB–TiC networks and trace Y 2 O 3 were fabricated by high-pressure high-temperature sintering at 5.5 GPa. The effects of sintering temperature and Y 2 O 3 addition on microstructure evolution, thermal stability, mechanical properties, high-temperature compression behavior, and cyclic oxidation resistance were investigated. At 1600 °C, the reaction between Ti64 and B 4 C led to the formation of a continuous TiB–TiC network along prior particle boundaries. The addition of 0.2 wt% Y 2 O 3 retained the network structure and refined the α–Ti matrix, decreasing the average grain size from 1.16 μm to 0.86 μm. The Y 2 O 3 -containing composite exhibited an ultimate compressive strength of 1771 MPa at room temperature and maintained a hardness of about 484 HV after annealing at 600 °C for 100 h. During high-temperature compression, it achieved a compressive stress of approximately 1098 MPa with 18.1% strain at 600 °C and sustained more than 45% strain at 800 °C without fracture. Cyclic oxidation tests showed that the Y 2 O 3 -containing composite had the lowest mass gain among the tested samples. Cross-sectional observations revealed a thinner oxide scale at 600 °C and retained Y–O-rich particles near the oxide/substrate region, suggesting improved local interfacial stability. These results demonstrate that combining a TiB–TiC network with trace Y 2 O 3 is an effective route to improve the high-temperature performance of Ti64-based composites.
✓ 已验证
产品关联
DOI
高影响因子
Small
·
2026
·
IF 12.1
Yueguang Fang,Chenxi Li,Xinqi Li,Lanling Xiu,Dingwen Xiao,Miao Wang,Lin Sun,Junwei Ye
Titanium-based materials hold great biomedical potential owing to excellent biocompatibility. But titanium diboride (TiB 2 ), an emerging metal boride, is rarely explored for antitumor use, and developing multifunctional TiB 2 -based nanoplatforms with enhanced catalytic activity is urgently needed. Herein, we constructed a nanoplatform (TiB 2 -PEG-DOX) by modifying TiB 2 nanosheets (TiB 2 NSs) with amino polyethylene glycol (NH 2 -PEG-NH 2 ) and loading doxorubicin (DOX) via electrostatic interaction. We first clarified the boron (B)-mediated Ti valence cycle: B regulates Ti electron transfer, promotes Ti 4+ reduction to Ti 2+ , enhancing H 2 O 2 -rich tumor microenvironment Fenton-like reaction to generate cytotoxic •OH for chemodynamic therapy (CDT). Meanwhile, TiB 2 -PEG-DOX shows 53.53% photothermal conversion efficiency under 808 nm near-infrared (NIR) irradiation for efficient photothermal therapy (PTT), and NIR further triggers on-demand DOX release. DOX accumulates at tumor sites via the enhanced permeability and retention (EPR) effect to exert chemotherapy (CT). In vitro, it eliminates 86.32% of HCT-116 colorectal cancer cells via CDT/PTT/CT synergy; in vivo, it achieves nearly complete tumor ablation in mice with excellent biocompatibility. This work provides a high-performance synergistic antitumor platform and establishes a B-modulated metal valence cycling paradigm, paving the way for titanium-based nanomedicines.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Journal of Environmental Chemical Engineering
·
2026
·Vol. 14
·期 2
·121708
·
IF 7.5
Liyang XIN,Jiahao ZHANG,Qian YANG,Liqiang QI
The treatment of high-chloride acidic industrial wastewater, such as that from wet flue gas desulfurization (WFGD) and metallurgical effluents, presents a significant environmental engineering challenge due to the high corrosivity of chloride and its interference with downstream processes. Bismuth oxide (Bi₂O₃)-based precipitation shows promise; however, it is hindered by severe surface passivation caused by BiOCl, which leads to self-limiting reactivity. In this study, we engineered a titanium-doped bismuth oxide (Bi₁₂TiO₂₀) photocatalyst that addresses this limitation through a synergistic mechanism of "adsorption–precipitation–photoregeneration." Under optimal dark conditions (pH = 0.1, [Cl⁻]₀ = 5000 mg/L, for 2 h), Bi₁₂TiO₂₀ achieved a chloride removal efficiency of 96.4 %, significantly exceeding that of pure Bi₂O₃, which was 64.4 %. The introduction of simulated solar irradiation at pH = 1.0 further enhanced the removal efficiency from 54.0 % to 67.2 %, demonstrating effective photo-enhancement. Comprehensive characterization techniques, including X-ray diffraction (XRD), scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS), X-ray photoelectron spectroscopy (XPS), and ultraviolet-visible-near-infrared (UV–Vis–NIR) spectroscopy, combined with kinetic modeling and electron localization function (ELF) calculations, revealed that Ti⁴⁺ serves as both a structural promoter—weakening Bi–O bonds to facilitate Bi³ ⁺ release—and a surface Lewis acid site that activates Cl⁻ adsorption. Importantly, photogenerated holes (h⁺) decompose the BiOCl passivation layer via the reaction BiOCl + 2 h⁺ → Bi³ ⁺ + ½O₂ + Cl₂↑, enabling in-situ regeneration of active interfaces and establishing a sustainable catalytic cycle. This work presents an efficient material for the initial bulk removal of chlorides, while also establishing a novel design paradigm for self-regenerative, energy-efficient water treatment technologies.
✓ 已验证
DOI
高影响因子
CERAMICS INTERNATIONAL
·
2026
·
IF 6
Mengwen Zhang,Fanyu Meng,Xiaoyu Chen,Na Cao,Lei Fan,Shoulei Yang
High-performance ceramic cutting tools require superior hardness and toughness under extreme temperatures; yet conventional sintering methods for Al 2 O 3 -Ti(C,N) composites often suffer from incomplete densification and grain coarsening. In this study, dynamic sinter forging (DSF) with oscillatory pressure amplitudes of 40 ± 40 MPa at 1600 °C is employed to regulate the densification behaviour and microstructural evolution of Al 2 O 3 -Ti(C,N) composites. The composite achieves a relative density above 99.9%, flexural strength of 1111 MPa, and hardness of 24.5 GPa at 15 Hz. A maximum fracture toughness of 5.44 MPa m 1/2 is obtained at 10 Hz. Microstructural observations reveal that moderate-frequency oscillation activate interfacial diffusion and stress-assisted plastic flow, promoting grain-boundary sliding and compact bonding to form a fine-grained and homogeneous structure. These results confirm that frequency-controlled DSF facilitates simultaneous enhancement of strength and toughness, providing a valid route for fabricating high-performance Al 2 O 3 -based cutting ceramics with optimized microstructural designs.
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DOI
高影响因子
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