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。

346,364+ SCI 论文 与阿拉丁产品引用相关
2,295,288.15 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。

热门产品

视图 列表 网格

显示第73至84个,产品总数75,974个

设置提升方向
氧
BIORESOURCE TECHNOLOGY · 2024 · IF 9.7

Response of anammox consortia to inhibition from high ferroferric oxide nanoparticles concentration and potential recovery mechanism

Li Zhang,Lixia Yang,Tingjun Dong,Jiachun Yang,Quanhao Dou,Shou-Qing Ni,Yongzhen Peng

The substantial discharge of ferroferric oxide nanoparticles (Fe 3 O 4 NPs) into sewage threatens the survival of functional microorganisms in wastewater treatment. This study elucidated responses of anaerobic ammonium oxidation (anammox) consortia to inhibition from high Fe 3 O 4 NPs concentration and recovery mechanisms. The nitrogen removal efficiency decreased by 20.3 % and recovered after 55 days under 1000 mg/L Fe 3 O 4 NPs concentration. Toxicity was attributed to reactive oxygen species (ROS) production. The excessive ROS damaged membrane integrity, nitrogen metabolism, and DNA synthesis, resulting in the inhibition of anammox bacteria activity. However, recovery mechanisms of anammox consortia activity were activated in response to 1000 mg/L Fe 3 O 4 NPs. The increase of heme oxygenase-1, thioredoxin, and nicotinamide adenine dinucleotide-quinone oxidoreductase genes alleviated oxidative stress. Furthermore, the activation of metabolic processes associated with membrane and DNA repair promoted recovery of anammox bacteria activity. This study provided new insights into NPs contamination and control strategies during anammox process.

CAS / MDL: 1317-61-9
研究领域: 环境科学 · 微生物学
✓ 已验证 产品关联 DOI PubMed 高影响因子
查看原文 查看 PubMed
Energy Technology · 2019 ·Vol. 7 ·期 9 ·1900374 · IF 3.163

Effect of Supports on the Redox Performance of NiFe2O4 in a Chemical Looping Process

Zhong Ma,Dewang Zeng,Shuai Zhang,Rui Xiao

NiFe 2 O 4 oxygen carrier (OC) presents higher oxygen carrying capacity than single metal oxides (NiO and Fe 2 O 3 ). However, the redox ability of NiFe 2 O 4 gets deactivated due to phase segregation. Herein, the investigation of the effect of supports (CeO 2 , CeZrO 2 , and ZrO 2 ) on the phase stability and the redox performance of NiFe 2 O 4 during the chemical looping (CL) process are presented. The structure of NiFe 2 O 4 -based OCs is characterized using different characterization methods. The CL reaction is conducted in a fixed-bed reactor at 900 °C under alternate 5% CO/N 2 and 5% O 2 /N 2 atmospheres. The results indicate that the redox performance and the phase stability of NiFe 2 O 4 -based OCs are significantly affected by the supports. According to experimental results, CeO 2 can improve the oxygen mobility of NiFe 2 O 4 . The CeO 2 –NiFe 2 O 4 OC has the best performance in terms of both recyclability and phase stability during the redox cycles. The results show that CeO 2 –NiFe 2 O 4 can reduce the tendency of Fe segregation due to the high concentration of oxygen vacancies. It can be reduced and reoxidized to the original crystalline phase of NiFe 2 O 4 . Nevertheless, the CeZrO 2 –NiFe 2 O 4 and ZrO 2 –NiFe 2 O 4 OCs have drawbacks related to serious sintering and phase segregation into Fe 2 O 3 .

研究领域: 材料科学 · 化学工程 · 能源化学 · 催化化学 · 无机化学
✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
Science China-Technological Sciences · 2022 ·Vol. 65 ·期 10 ·2317-2324 · IF 3.903

Oxygen-vacancy-rich TiO2 enables highly active and durable water electrolysis of urchin-like RuO2 catalyst

Gao HongMei,Xiao MeiLing,Li GuoQiang,Gao LiQin,Meng QingLei,Luo ZhaoYan,Luo ErGui,Liu ChangPeng,Jin Zhao,Ge JunJie,Xing Wei

The material innovation is prerequisite to accelerating sluggish oxygen evolution reaction (OER) kinetics, thus promoting the realization of hydrogen energy community. Herein, we develop an oxygen-vacancy-rich TiO 2 supported RuO 2 catalyst (RuO 2 @r-TiO 2 ) towards improved OER activity and stability. The oxygen vacancy on TiO 2 not only supplies electrons to produce lower valence Ru, but also provides sufficient anchoring site for the deposition of RuO 2 nanocrystal. Beyond that, it can generate strong electronic interaction between TiO 2 and supported RuO 2 , and thereby tailors the intermediates’ adsorption energy on the RuO 2 surface. As a result, the derived RuO 2 @r-TiO 2 catalyst exhibits superior OER activity and stability with the overpotential of 211 mV at a current density of 10 mA cm −2 and negligible activity degradation after 6 h operation, outperforming the non-oxygen-vacancy counterpart (223.3 mV, 12.75% activity loss) and RuO 2 catalyst (234.6 mV, 42.86% activity loss).

研究领域: 材料科学 · 电化学 · 催化化学 · 能源材料 · 纳米科技 · 物理化学
✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
Journal of Inorganic and Organometallic Polymers and Materials · 2019 ·Vol. 30 ·期 5 ·1553-1565 · IF 1.637

Preparation of Epoxidized Natural Rubbers with Improved Aging Resistance by Covalently Bridging Graphene and Antioxidants

Liu Yong,Wei Ya,Liu Rongjuan,Liang Zhaopeng,Yang Jun,Zhang Ruilong,Zhou Zhiping,Nie Yijing

A new kind of epoxidized natural rubber (ENR) nanocomposites with enhanced aging resistance by the inclusion of a non-migratory anti-aging agent was prepared. The non-migratory anti-aging agent was obtained by immobilizing antioxidant molecules on graphene oxide (GO) surface using a silane coupling agent. In this way, the diffusion of the small-molecule antioxidants is restricted, leading to low loss of antioxidants in rubber service and the improvement of rubber aging resistance. GO, due to its unique two-dimensional planar structure, forms barrier layers inside the composite to prevent gas diffusion, which also contributes to the enhancement in anti-aging properties. In addition, hydrogen bond networks form between ENR chains and GO nanosheets, limiting the movement of the non-migratory anti-aging agents and improve their stability in rubber matrix. Our experimental results demonstrated that the non-migratory anti-aging agents can endow rubbers with better resistance to thermo-oxidative aging than the conventional antioxidants with a same amount.

CAS / MDL: 101-54-2 919-30-2
研究领域: 材料科学 · 高分子化学
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
SENSORS AND ACTUATORS B-CHEMICAL · 2024 · IF 8

Oxygen-defect rich SnO2-based homogenous composites for fast response and recovery hydrogen sensor

Qiaoling Xing,Xujie Chen,Yong Cai,Ming Zhang

As a kind of green energy, hydrogen (H 2 ) has been widely concerned and applied by people. One of the biggest challenges for sensing applications is the quick detection of hydrogen leaks or their release in various conditions, particularly in large electric vehicle batteries. This study successfully constructed a quick response and recovery hydrogen sensor based on the In 2 O 3 -SnO 2 heterojunction. The response and recovery time of the In 2 O 3 -SnO 2 hydrogen sensor is 1.1/1.9 s to 50 ppm H 2 . This is reduced to 11.0 %/9.5 % compared to the SnO 2 hydrogen sensor. This sensor's remarkable gas detecting properties are mainly attributed to the In 2 O 3 -SnO 2 heterojunction creation, crystal structure modification, and increased specific surface area (92.9 m 2 /g). Homogenous In 2 O 3 -SnO 2 nanocomposites contain more oxygen defects, which is the primary factor enhancing the sensor's ability to detect gases. Firstly, indium ions are incorporated in the lattice of SnO 2 results in lattice distortion and enhances the presence of oxygen deficiency in the composites, which plays a pivotal role in achieving rapid response and recovery of the sensor. Secondly, In 2 O 3 -SnO 2 heterostructures promote rapid adsorption of oxygen molecules and target gases by facilitating effective electron mobility on their surface. The quicker response and recovery times of hydrogen sensors based on In 2 O 3 -SnO 2 heterojunctions are observed. This innovative approach to creating fast-responding gas sensors highlights the promise of heterojunction-based hydrogen sensors for real-time H 2 monitoring and opens up new research directions.

CAS / MDL: 207398-97-8
研究领域: 材料科学 · 传感器技术
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
APPLIED SURFACE SCIENCE · 2024 · IF 6.3

Oxygen defect engineering in Pt/CeO2 catalyst for promoted selective oxidation of HMF to FDCA

Fuyuan Qi,Weiping Yang,Lan-Lan Lou,Shuangxi Liu,Kai Yu

Oxygen vacancies play an important role in the oxidation of biomass-derived alcohols and aldehydes using ceria-based catalysts. In this study, a highly oxygen vacancy-defective Pt/H-CeO 2 catalyst was synthesized by a straightforward strategy that involved the control of the addition of ascorbic acid and nitric acid. The addition of ascorbic acid, which acted as a pore-forming agent, promoted the hydrolysis, crystallization, and subsequent growth of Ce precursor salt, resulting in the synthesis of H-CeO 2 with abundant oxygen vacancy defects and a porous thin sheet-like morphology. However, the addition of nitric acid significantly inhibited the generation of oxygen vacancy defects. The obtained H-CeO 2 exhibited significantly increased oxygen vacancy content, active oxygen species, and specific surface area compared with CeO 2 with lower oxygen vacancy defects (L-CeO 2 ). These remarkable features led to enhanced catalytic activity of Pt/H-CeO 2 for the oxidation of 5-hydroxymethylfurfural (HMF) compared with Pt/L-CeO 2 . This can be mainly attributed to the enhanced adsorption and activation of O 2 molecules by abundant oxygen vacancies, allowing more active oxygen species to participate in the dehydrogenation of HMF. This work provides an example of oxygen defect engineering for ceria-based catalysts to boost the catalytic selective oxidation performance.

研究领域: 催化化学 · 材料科学
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
Pharmaceuticals · 2024 ·Vol. 17 ·期 10 ·1257 · IF 4.3

Antioxidant and Pro-Oxidant Properties of Selected Clinically Applied Antibiotics: Therapeutic Insights

Tibor Maliar,Marcela Blažková,Jaroslav Polák,Mária Maliarová,Eva Ürgeová,Jana Viskupičová

Background: The balance between antioxidants and pro-oxidants plays a significant role in the context of oxidative stress, influenced by both physiological and non-physiological factors. Objectives: In this study, 18 prescribed antibiotics (including doxycycline hydrochloride, tigecycline, rifampicin, tebipenem, cefuroxime, cefixime, potassium clavulanate, colistin, ampicillin, amoxicillin, amikacin, nalidixic acid, azithromycin, pipemidic acid trihydrate, pivmecillinam, aztreonam, fosfomycin sodium, and ciprofloxacin) were subjected to simultaneous determination of antioxidant and pro-oxidant potential to assess if pro-oxidant activity is a dominant co-mechanism of antibacterial activity or if any antibiotic exhibits a balanced effect. Methods: This study presents a recently developed approach for the simultaneous assessment of antioxidant and pro-oxidant potential on a single microplate in situ, applied to prescribed antibiotics. Results: Ten antibiotics from eighteen showed lower antioxidant or pro-oxidant potential, while five exhibited only mild potential with DPPH50 values over 0.5 mM. The pro-oxidant antioxidant balance index (PABI) was also calculated to determine whether antioxidant or pro-oxidant activity was dominant for each antibiotic. Surprisingly, three antibiotics—doxycycline hydrochloride, tigecycline, and rifampicin—showed significant measures of both antioxidant and pro-oxidant activities. Especially notable was tebipenem, a broad-spectrum, orally administered carbapenem, showed a positive PABI index ratio, indicating a dominant antioxidant over pro-oxidant effect. Conclusions: These findings could be significant for both therapy, where the antibacterial effect is enhanced by radical scavenging activity, and biotechnology, where substantial pro-oxidant activity might limit microbial viability in cultures and consequently affect yield.

研究领域: 药理学 · 微生物学 · 生物化学
✓ 已验证 DOI PubMed 高影响因子
查看原文 查看 PubMed
RSC Advances · 2017 ·Vol. 7 ·期 81 ·51142-51150 · IF 3.108

An Fe3O4@P4VP@FeCl3 core–shell heterogeneous catalyst for aerobic oxidation of alcohols and benzylic oxidation reaction

Ruilian Li,Jian Zhao,Fengxia Yang,Yingchao Zhang,Daniele Ramella,Yu Peng,Yi Luan

A novel magnetic Fe3O4@P4VP(poly(4-vinylpyridine))@FeCl3 core–shell structure was successfully synthesized. Its Fe3O4@P4VP core was initially prepared via polymerization of 4-vinyl pyridine on the surface of Fe3O4 microspheres. The successful introduction of the FeCl3 moiety as a catalytic active site was achieved through coordination interaction between P4VP and FeCl3. The obtained Fe3O4@P4VP@FeCl3 catalyst was applied in the selective oxidation of alcohols using molecular oxygen as the oxidant. It was shown that a variety of alcohol substrates is tolerated under optimized reaction conditions. Additionally, benzylic oxidation of hydrocarbon compounds was also evaluated using Fe3O4@P4VP@FeCl3 as the catalyst and tBuOOH as the oxidant, achieving high yields and very good selectivities. The heterogeneity of the Fe3O4@P4VP@FeCl3 core–shell catalyst was tested and the initial activity was maintained after five reuses.

研究领域: 化学 · 催化科学
✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
Catalysts · 2023 ·Vol. 13 ·期 7 ·1078 · IF 3.9

Preparation and Photocatalytic CO Oxidation Performance Study of Au/Oxygen-Deficient (Anatase/B-Phase) TiO2 Heterojunction Microspheres

Ze Hong,Jingying Ouyang,Jiaxin Li,Han Zheng,Ying Liu

Multi-heterojunctions are more promising than single heterojunctions in photocatalysis due to the availability of more interfaces between each component. However, photocatalytic activity is highly dependent on the contact mode of individual components. In this work, we assembled gold nanoparticles/oxygen-deficient (anatase/B-phase) TiO2multi-heterojunction microspheres using spray pyrolysis and focused on their contact mode-governed photocatalytic activity. The results reveal that using oxygen-deficient (anatase/B-phase) TiO2microspheres as building blocks could significantly enhance the absorption of visible light and the photocatalytic activity of a gold–TiO2system toward the photocatalytic carbon monoxide oxidation. Furthermore, loading gold nanoparticles onto B-phase TiO2could facilitate a more prominent enhancement of activity than that of pure B-phase TiO2, benefiting from the two-electron reduction of oxygen at the interface of TiO2/Au. Meanwhile, the high crystallinity of B-phase TiO2microspheres allows for a gold loading amount of 1 wt% in the gold/(anatase/B-phase) TiO2system, which is 1.67 times more active than pure B-phase TiO2microspheres, in the photocatalytic oxidation of carbon monoxide to generate carbon dioxide.Keywords:photocatalytic carbon monoxide oxidation;B-phase TiO2;oxygen-deficient;microspheres

研究领域: 材料科学 · 环境科学
✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
SEPARATION AND PURIFICATION TECHNOLOGY · 2025 · IF 9

Stimulating MgO defects exposure by nitrogen doping within activated carbon to enhance H2S catalytic oxidation

Yinghong Luo,Caiyue Zhao,Wanglai Cen,Yanshi Zhang,Guannan Huo,Xiaoya Wang,Hanyue Ma,Yipeng Wang,Daiqi Ye,Junliang Wu

Metal oxide-loaded catalysts are extensively used for room temperature catalytic oxidation of H 2 S due to their strong affinity for H 2 S, but tend to exhibit poor activity due to uneven dispersion. Herein, a series of nitrogen and MgO co-modified activated carbon was synthesized using the co-impregnation method. The desulfurization efficiency of the optimal material exceeded the individual contributions of nitrogen doping and MgO loading by nearly 25 %, achieving a remarkable 742.67 mg/g. This enhancement was partly attributed to the synergistic interaction between electron-rich pyridine N and MgO, promoting oxygen vacancies formation, which favored O 2 activation. Moreover, the substitutional nitrogen defects in MgO induced the formation of adjacent magnesium vacancies, increasing the number of strong basic sites favorable for H 2 S dissociation. The modification strategy adopted in this study is also applicable to commercial activated carbon, providing a feasible approach for developing cost-effective low-temperature technology.

研究领域: 环境科学 · 材料科学
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
ACS Applied Materials & Interfaces · 2024 · IF 8.3

Exploring the Facet-Dependent Structural Evolution of Pt/CeO2 Catalysts Induced by Typical Pretreatments for CO Oxidation

Yao Lv,Aoran Li,Jiajie Ye,Haifeng Wang,Peijun Hu,Kuan-Wen Wang,Yun Guo,Xuan Tang,Sheng Dai

Atomic-scale insights into the interactions between metals and supports play a crucial role in optimizing catalyst design, understanding catalytic mechanisms, and enhancing chemical conversion processes. The effects of oxide support on the dynamic behavior of supported metal species during pretreatments or reactions have been attracting a lot of attention; however, very less systematic integrations are carried out experimentally using real catalysts. In this study, we here utilized facet-controlled CeO2 as examples to explore their influence on the supported Pt species (1.0 wt %) during the reducing and oxidizing pretreatments that are typically applied in heterogeneous catalysts. By employing a combination of microscopy, spectroscopy, and first-principles calculations, it is demonstrated that the exposed crystal facets of CeO2 govern the evolution behavior of supported Pt species under different environmental conditions. This leads to distinct local coordinations and charge states of the Pt species, which directly influence the catalytic reactivity and can be leveraged to control the catalytic performance for CO oxidation reactions.

研究领域: 催化化学 · 材料科学
✓ 已验证 DOI PubMed 高影响因子
查看原文 查看 PubMed
APPLIED SURFACE SCIENCE · 2022 · IF 7.392

Mechanochemical construction of Bi1-xLaxOI solid solution with abundant oxygen vacancies for enhanced photocatalytic oxidation of inorganic/organic arsenic

Zhao Li,Lei Wu,Min Chen,Qiwu Zhang,Shujuan Dai,Tonglin Zhao

Bismuth oxyiodide is one of the bismuth-based semiconductors which exhibits narrow band gaps and excellent visible light response, however modification strategies are usually desired for improving its photocatalytic reactivity. In this context, introduction of valuable components into the interlayer of BiOI is expected to work, considering its typical layered structure. In this case, mechanochemical synthesis of BiOI, with simultaneous introduction of lanthanum into its interlayer to form Bi 1-x La x OI, was conducted for the first time, and arsenic (As(III)) was selected to evaluate the photocatalytic reactivity, demonstrating excellent reaction efficiency for arsenic oxidation under a mild condition. Characterizations confirmed the incorporation of La and the presented well crystalline structure of Bi 1-x La x OI, and revealed its better visible light absorption capacity than raw BiOI. Besides the excellent electronic conductivity of Bi 0.9 La 0.1 OI, photogenerated holes (h + ) and superoxide radical species (· O 2 - ) were characterized by electron spin resonance (ESR) test, to act as predominant reactive groups during the photo-induced oxidation reaction. These findings provided a novel concept for the interlayer decoration of BiOI, and offered an alternative approach to develop its potential application for the removal of hazardous arsenic pollutants.

研究领域: 环境科学 · 材料科学
✓ 已验证 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。