文献检索

查找使用阿拉丁产品的科研文献

检索与阿拉丁产品相关的同行评审论文、DOI、PubMed 编号、期刊、作者、CAS 号及研究领域。

科研影响力快照

与阿拉丁产品相关的已发表科研成果

在搜索之前,这些指标可帮助访客快速了解产品关联科研的规模与质量。

346,438+ SCI 论文 与阿拉丁产品引用相关
2,295,919.25 总影响因子 匹配文献记录中影响因子的总和
81.20 最高期刊影响因子 匹配期刊中的最高 IF
6.63 平均期刊影响因子 匹配文献的平均 IF

参考指标 指标基于阿拉丁文献引用数据库及期刊影响因子记录。文献关联仅供科研参考,请以原始文献为准。

产品列表

视图 列表 网格

显示第817至828个,产品总数1,103个

设置提升方向
Ti
APPLIED ORGANOMETALLIC CHEMISTRY · 2020 ·Vol. 34 ·期 6 ·e5612 · IF 3.14

Degradation of p-aminophenol wastewater using Ti-Si-Sn-Sb/GAC particle electrodes in a three-dimensional electrochemical oxidation reactor

Na Zhang,Jiaqi Bu,Yong Meng,Jia Wan,Lu Yuan,Xin Peng

In this study, Ti-Si-Sn-Sb/GAC particle electrodes were prepared by sol–gel method. The particle electrodes were characterized by SEM, XRD, EDX, and BET then used to carry out three-dimensional (3D) electrocatalytic oxidation degradation on simulated refractory p-aminophenol (PAP) wastewater. The effects of initial pH, cell voltage, aeration flow rate and initial PAP concentration on degradation experiments were investigated. Under the optimal conditions, the PAP and COD removal rates were 89.45% and 75.17% respectively. In addition, the possible degradation mechanism of PAP was further investigated by UV–Vis and HPLC. Finally, it was found that the Ti-Si-Sn-Sb/GAC particle electrodes with high catalytic activity and excellent stability could significantly improve the PAP wastewater removal efficiency.

CAS / MDL: 123-30-8
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF HAZARDOUS MATERIALS · 2019 · IF 7.65

Enhanced electro-oxidation/peroxone (in situ) process with a Ti-based nickel-antimony doped tin oxide anode for phenol degradation

Chao Qu,Ghulam Sarwar Soomro,Na Ren,Da-wei Liang,Shan-fu Lu,Yan Xiang,Shu-jun Zhang

Recently, a novel proof-of-concept oxygen reduction reaction (ORR) based electro-oxidation (EO) process has been developed, which was accomplished by integrating anodic electrochemical oxidation coupled with an in situ electro-peroxone process, by harnessing the anodic by-product O 3 reacted with ORR cathode generated H 2 O 2 . To further enhance EO coupled in situ electro-peroxone, a nickel and antimony doped tin oxide anodic catalyst layer, namely NATO, was fabricated on Ti mesh to improve anodic oxidation and reinforce the generation of O 3 , thus promoting in situ Electro-peroxone. As a result, O 3 generation rate was enhanced by 12.6%. Complete phenol , as a model organic compound, and 95% of TOC removal were achieved, respectively, during ORR-EO. Through kinetics and instrument analysis, results show that the amount of intermediates accumulated during phenol degradation was much less in this Ti/NATO based ORR-EO system than in a traditional EO system. Moreover, 35.7% of the energy consumption was saved for ORR-EO, owing to its reduced applied voltage and the enhanced in situ electro-peroxone process.

✓ 已验证 产品关联 DOI PubMed 高影响因子
查看原文 查看 PubMed
CATALYSIS LETTERS · 2019 ·Vol. 149 ·期 9 ·2586-2596 · IF 2.372

Preparation of the Hierarchical Ti-Rich TS-1 via TritonX-100-Assisted Synthetic Strategy for the Direct Oxidation of Benzene

Shen Xiaohua,Wang Jingjing,Liu Miaoqing,Li Mengzhe,Lu Jianjun

Abstract A new route to synthesis hierarchical Ti-rich TS-1 with uniform intracrystalline mesopores, uniform crystal size and the higher Ti content has been developed by using the environmental-friendly and cheap surfactant Triton X-100 as the assisted template agent and (NH 4 ) 2 CO 3 as crystallization-mediating agent. In this way, the surface area and pore volume of the resulting materials can be adjusted by the Triton X-100 content. The catalytic properties of the Nano-size hierarchical Ti-rich TS-1 were investigated by hydroxylation of benzene to phenol with H 2 O 2 as oxidizing agent and deionized water as solvent. Due to the combination of hierarchical pores and high titanium content, the hierarchical Ti-rich TS-1 shows improved catalytic activity in the oxidation of benzene. Graphical Abstract

CAS / MDL: 71-43-2 7722-84-1
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF ALLOYS AND COMPOUNDS · 2020 · IF 4.65

Effect of different transition metal fluorides TMFx (TM=Nb, Co, Ti) on hydrogen storage properties of the 3NaBH4-GdF3 system

Tianping Huang,Jianxin Zou,Huabing Liu,Wenjiang Ding

Three kinds of transition metal fluorides TMF x (TM = Nb, Co, Ti) were introduced into the 3NaBH 4 -GdF 3 hydrogen storage system via mechanical milling. Their effects on the hydrogen storage behaviors of 3NaBH 4 -GdF 3 were systematically investigated by means of DSC and volumetric methods. All TMF x exhibited promoting effect on hydrogen desorption properties of 3NaBH 4 -GdF 3 to different degrees, especially when NbF 5 or TiF 3 was added. For example, the hydrogen desorption peak temperature was decreased by 17 °C with doping 3 mol% of NbF 5 . Besides, TiF 3 improved also the hydrogen absorption capacity and reversibility of 3NaBH 4 -GdF 3 . Based on XRD analyses, the role of TMF x on the dehydrogenation and the promoting effect of TiF 3 on the reversibility of 3NaBH 4 -GdF 3 were clarified. This work helped to understand the combination effect of rare earth metal fluoride (GdF 3 ) and transition metal fluorides on the reversible hydrogen storage properties of NaBH 4 .

CAS / MDL: 13765-26-9 16940-66-2
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
MATERIALS SCIENCE AND ENGINEERING A-STRUCTURAL MATERIALS PROPERTIES MICROSTRUCTURE AND PROCESSING · 2018 · IF 3.414

Enhanced compressive strength and tailored microstructure of selective laser melted Ti-46.5Al-2.5Cr-2Nb-0.5Y alloy with different boron addition

Wei Li,Ming Li,Yi Yang,Qingsong Wei,Daosheng Cai,Jie Liu,Chunze Yan,Yusheng Shi

The microstructures and compressive properties of Ti-46.5Al-2.5Cr-2Nb-0.5Y alloy with varied boron (B) addition processed by selective laser melting (SLM) had been systematic studied. With increasing the B content from 0 to 2 wt%, the average grain size of SLM-processed Ti-46.5Al-2.5Cr-2Nb-0.5Y/B composites decreased from 16.64 µm to 5.66 µm, meanwhile, the {0001} texture index and high angle grain boundaries (HAGBs) increased from 10.78 and 87.9% to 22.69 and 94.4%. The phase evolution mechanism of Ti-46.5Al-2.5Cr-2Nb-0.5Y/B composites during the SLM process can be summarized as: firstly, β and B phases precipitated out from the liquid phase, then the β phase transformed to α phase and part of the α phase transferred to γ phase, later, some new phases of TiB 2 and AlB 2 emerged by the diffusion mechanism of B, Ti and Al atoms, and then the β and α phases orderly transformed to B 2 and α 2 , lastly, the γ, B 2 , B, TiB 2 , AlB 2 phases in a range of several hundred nanometers were randomly distributed within the α 2 matrix. Due to the grain refinement strengthening mechanism, the compressive strength and strain of Ti-46.5Al-2.5Cr-2Nb-0.5Y/B parts increased to the maximum of 1610.53 MPa and 5.17%.

✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
APPLIED SURFACE SCIENCE · 2018 · IF 4.439

Investigation on adhesion strength and corrosion resistance of Ti-Zr aminotrimethylene phosphonic acid composite conversion coating on 7A52 aluminum alloy

Qi Liu,Xiaoming Cao,An Du,Ruina Ma,Xiaoran Zhang,Tingting Shi,Yongzhe Fan,Xue Zhao

In this paper, a chromate free conversion coating based on titanium/zirconium salts and aminotrimethylene phosphonic acid (ATMP) was prepared on 7A52 aluminum alloy. The morphology and composition of conversion coating were investigated by test measurements of SEM、EDS、XRD and FT-IR. The adhesion strength between aluminum matrix and subsequent epoxy primer was tested directly. The roughness and wettability of conversion coating were also detected to indirectly characterize the adhesion strength from another side. The electrochemical tests and neutral salt spray tests were also conducted to measure the corrosion resistance of the prepared conversion coating. Results reveal that a uniform and dense conversion coating consisted by metal oxides and other salts is obtained on the surface of 7A52 aluminum alloy. Significantly, the adhesion strength between matrix and epoxy primer increases from 7.97 MPa to 16.23 MPa, which dues to the increase of surface roughness and the improvement of wettability. In addition, the neutral salt spray test time of the conversion coating reaches as long as 120 h. Three orders of magnitudes decrease of current density proves the excellent corrosion resistance of conversion coating, which is also confirmed by electrochemical impedance spectroscopy test. This dues to the barrier property of conversion coating, preventing the corrosive solution to have a direct contact with aluminum matrix. Anyhow, both the adhesion strength and corrosion resistance are greatly reinforced by the existence of conversion coating.

CAS / MDL: 16923-95-8 16919-27-0
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
POWDER TECHNOLOGY · 2018 · IF 3.23

In-situ preparation and formation of TiB/Ti-6Al-4V nanocomposite via laser additive manufacturing: Microstructure evolution and tribological behavior

Chao Cai,Chrupcala Radoslaw,Jinliang Zhang,Qian Yan,Shifeng Wen,Bo Song,Yusheng Shi

In this study, the in-situ synthesized TiB/Ti-6Al-4Vceramic-matrix nanocomposites with greatly enhanced hardness and wear resistant property have been prepared via selective laser melting (SLM) using a simple mixture of microsized Ti-6Al-4V and TiB 2 powders. In order to provide a valuable reference for fabricating TiB/Ti-6Al-4V parts with metallographic features, effects of reinforcement content on microstructure and mechanical properties have been systematically investigated. It is found that during SLM process, the additive particles TiB 2 are totally transformed into need-like nanoscaled TiB phase, and the microstructure of composites is composed of mutual parallel strips architecture with TiB rich in some regions but lean in the other regions. The SLM-producedTiB/Ti-6Al-4 V composites exhibit superior nanohardness of 6.0 GPa, which is much higher than its traditional sintering counterpart. Moreover, the in-site synthesized TiB reinforcement can remarkably improve in the wear resistance properties, the wear loss of TiB-free sample is approximately 2 times than that of the sample with 3 wt% TiB 2 .

CAS / MDL: 12045-63-5
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
ACS Catalysis · 2013 · IF 5.265

Highly Selective Liquid-Phase Oxidation of Cyclohexane to KA Oil over Ti-MWW Catalyst: Evidence of Formation of Oxyl Radicals

Wen-Juan Zhou,Raphael Wischert,Kai Xue,Yu-Ting Zheng,Belén Albela,Laurent Bonneviot,Jean-Marc Clacens,Floryan De Campo,Marc Pera-Titus,Peng Wu

Various types of Ti-containing zeolites, i.e., Ti-MWW, TS-1, Ti-MOR, and Ti-BEA, have been evaluated as candidates for the liquid-phase oxidation of cyclohexane using t-butyl hydroperoxide (TBHP, 7–8 wt %) as model oxidant. Ti-MWW zeolite displayed the highest activity for cyclohexanol and cyclohexanone (KA oil) with an overall selectivity higher than 90% at 80 °C, making this catalyst a candidate of choice for industrial KA oil production by deperoxidation of cyclohexyl hydroperoxide. The effect of the reaction temperature, reaction time, catalyst amount, and catalyst stability on Ti-MWW was surveyed in detail. The Ti-MWW catalyst showed a stable performance and could be recycled at least four times without detectable Ti leaching and loss of structural stability. The active sites for cyclohexane oxidation appeared to be located near external 12-ring cups in the Ti-MWW framework as suggested by a series of position-selective poisoning tests with tripropyl- and triphenylamine, impelling cyclohexane diffusion within the internal 10-ring channels. EPR experiments supported by DFT calculations suggested the coexistence of both Ti(IV)-OO• (peroxyl) and Ti(IV)-O• (oxyl) species generated through bimolecular pathways, implying simultaneously (SiO)3Ti(OOtBu) species and tBuOOH. The catalytic activity was strongly inhibited in the presence of alkenes, leading to the preferential formation of the epoxidation product with no detectable formation of radicals. Notably, this is the first time that oxyl species have been detected particularly with the help of DFT calculations. Predicted differences of g tensors between peroxyl and oxyl species at various hydration levels in the presence of cyclohexane were consistent with the EPR spectra.

CAS / MDL: 110-83-8 286-20-4
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
RSC Advances · 2015 ·Vol. 5 ·期 103 ·84856-84864 · IF 3.84

Electrochemical degradation of perfluorooctanoic acid (PFOA) by Yb-doped Ti/SnO2–Sb/PbO2 anodes and determination of the optimal conditions

Qianchi Ma,Lei Liu,Wei Cui,Ruifeng Li,Tingting Song,Zhaojie Cui

Model aqueous solutions of perfluorooctanoic acid (PFOA, 100 mg L−1) were electro-oxidized in a homemade container. The electrocatalytic behavior and anodic performance of Ti/SnO2–Sb/Yb–PbO2, Ti/SnO2–Sb–PbO2 and Ti/SnO2–Sb–Yb anodes in sodium electrolytes were compared. The SnO2–Sb/Yb–PbO2 anode demonstrated better electrocatalytic performance compared with the SnO2–Sb–PbO2 and SnO2–Sb–Yb electrodes in terms of both degradation and defluorination. Then a systematic experimental study was designed as follows to analyze the influencing factors: initial concentration of PFOA (10 mg L−1 to 200 mg L−1), current density (1 mA cm−2 to 40 mA cm−2), initial pH value (3 to 11) and electrode distance (5 mm to 20 mm). After a 150 min electrolysis, the optimum reaction conditions were obtained and the degradation and defluorination ratios reached 95.11 ± 3.9% and 75.7 ± 2.8%, respectively. Under the optimum conditions, the degradation of PFOA followed pseudo-first-order kinetics (0.0193 min−1) and the degradation half-life was 35.9 min. The produced F− was measured using a fluoride ion selective electrode, whereas the intermediate PFCAs with short-chain lengths were measured using HPLC-MS. A detailed degradation pathway was proposed in this study by analyzing the intermediates and the recovery of fluoride.

CAS / MDL: 422-64-0
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
CHEMICAL ENGINEERING JOURNAL · 2017 · IF 6.216

Synthesis, characterization and adsorptive denitrogenation performance of bimodal mesoporous Ti-HMS/KIL-2 composite: A comparative study on synthetic methodology

Haiyan Song,Jiang-An You,Bin Li,Chunxia Chen,Jie Huang,Jin Zhang

Novel titanosilicate composites with bimodal mesopores using molecular sieves Ti-HMS and Ti-KIL-2 as structural components were successfully synthesized by two-step and dual-template methods in a comparative study. The as-synthesized Ti-HMS/KIL-2 samples were characterized by a series of techniques including X-ray diffraction, UV–vis, N 2 sorption and scanning electronic microscopy, and their performance was tested in adsorptive denitrogenation for model fuel containing pyridine or quinoline. Although Ti-HMS/KIL-2 composites were constructed following the different pathway of self-assembly, most of them obtained coexisting properties and structures of Ti-HMS and Ti-KIL-2, as well as the intact framework Ti in tetrahedral coordination. A key finding is that the mesopores size of Ti-KIL-2 component in the composite can be regulated via the introduction of Ti-HMS precursor or organic template dodecylamine. Especially, the composites of dual-template method presented hierarchical mesopores with obvious bimodal distribution. In addition to constructing the hierarchical structure, introduction of Ti-HMS into Ti-KIL-2 matrix improved the adsorptive denitrogenation performance, which was influenced by the synthetic strategy of Ti-HMS/KIL-2. The target adsorbates achieved the best match with the adjustable pores of Ti-HMS/KIL-2. Therefore, (0.6 D )Ti-HMS/KIL-2 and (0.5 T )Ti-HMS/KIL-2 as the optimized adsorbents obtained remarkable adsorption efficiency respectively for pyridine and quinoline. Essence of the adsorptive denitrogenation process was revealed via the adsorption isotherms and the adsorption thermodynamics. Finally, Ti-HMS/KIL-2 composites achieved the improvement in hydrothermal stability and recyclability during adsorption of pyridine and quinoline, and exhibited the potential of industrial application.

✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY · 2016 ·Vol. 92 ·期 4 ·827-833 · IF 2.738

Electro-generation of NaOH–H2SO4 and simultaneous degradation of Acid orange 7 from Na2SO4-containing wastewater by Ti/IrO2 electrodes

Jinxi Feng,Shenyu Lan,Chunyang Yao,Ya Xiong,Shuanghong Tian

BACKGROUND Electro-generation of NaOH and H 2 SO 4 with organic compound-free Na 2 SO 4 wastewater has been known for many years, but actually, lots of Na 2 SO 4 wastewater contains organic pollutants, such as black liquor, dyeing and sulphonating wastewater etc., therefore, there is a strong demand for investigations on performance and effect of the organic pollutants in electrochemically splitting Na 2 SO 4 into H 2 SO 4 and NaOH from these wastewaters. RESULTS Co-electrolysis of Na 2 SO4 (1.13 mol L −1 ) and AO7 (50 ∼ 500 mg L −1 ) was investigated in a diaphragm cell with IrO 2 -coated Ti electrodes. It was found that the concentrations of the resulting NaOH and H 2 SO 4 could remain at about 0.73 mol L −1 and 0.36 mol L −1 , respectively, although the COD removal was increased from 50.3 mg L −1 to 166.3 mg L −1 with the increase of AO7 concentration, for 120 min. CONCLUSION In a diaphragm cell with IrO 2 -coated Ti electrodes, NaOH and H 2 SO 4 could be effectively generated, and simultaneously, AO7 could also be degraded for the wastewater containing Na 2 SO 4 and AO7. Interestingly, the electro-generation of NaOH and H 2 SO 4 was not significantly affected by the occurrence and degradation of AO7 in the range 0–500 mg L −1 . The phenomenon of constant acid–base yield contributed to the independence of the main acid-generating reactions on the electro-oxidation of AO7. © 2016 Society of Chemical Industry

✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
APPLIED SURFACE SCIENCE · 2024 · IF 6.3

Inkless printing and advanced dynamic information anti-counterfeiting via photochromic system based on solid-state Zr/Ti-MOF@WO3 heterojunctions

Bingbing Cui,Guodong Fu

Given that heterojunction engineering is an effective method for improving the separation efficiency of photoexcited electrons in WO 3 -based photochromic systems, a series of solid-state photochromic Zr/Ti-MOF@WO 3 heterojunctions prepared via a facile hydrothermal strategy, where Zr/Ti-MOF with photosensitivity and chemical stability was selected as template to load WO 3 . Zr/Ti-MOF@WO 3 heterojunctions were verified as nanoparticles filled with thin layer structure and WO 3 was diffused into the Zr/Ti-MOF planar. The appropriate conductive band energies facilitate the transport of photostimulated electrons from Zr/Ti-MOF to WO 3 , resulting in a fast photresponse in color changes (it only takes 1 s). In addition, a carrier for information storage and data dynamic encryption was developed on the basis of the photochromic Zr/Ti-MOF@WO 3 heterojunctions. This work presents a promising way to improve the electron/holes separation efficiency by constructing unique heterojunctions and further explore novel WO 3 -based photochromic systems and broaden their applications in rewritable media and data security.

✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
已复制

文献关联基于可获得的产品、CAS、DOI 及引用记录。收录不代表作者或出版方对阿拉丁产品的背书,请以原始文献为准。