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JOURNAL OF THE ELECTROCHEMICAL SOCIETY · 2022 ·Vol. 169 ·期 12 ·126508 · IF 4.386

Hollow Spherical NiCo2O4 and Gold Nanoparticle Composite for Electrochemical Non-Enzymatic Glucose and H2O2 Sensing

Li Feng,Yan Xu,Wanting Deng,Yadong Wang,Xiaoqin Min,Xiaoyun Lin,Yongnian Ni

A novel electrochemical non-enzymatic sensor for glucose and H2O2 based on metal organic framework (MOF)-derived cobalt-nickel bimetallic oxides (NiCo2O4) and gold nanoparticle (AuNPs) composite modified glassy carbon electrode (GCE) was fabricated in this paper. The structure and morphology of the prepared materials was successfully characterised by X-ray diffraction (XRD), element mapping images and scanning electron microscopy (SEM). Moreover, the electrocatalytic activity for glucose and H2O2 was investigated at the NiCo2O4/AuNPs/GCE using cyclic voltammetry (CV) and amperometric i–t technique. The catalytic currents for glucose and H2O2 are proportional to their concentrations in the range of 0.2 μM–581 μM and 0.5 μM–1774.5 μM, respectively. The corresponding limits of detection (LOD) were calcuated be 0.0081 μM and 0.181 μM for glucose and H2O2. Furthermore, the NiCo2O4/AuNPs/GCE shows excellent stability, reproducibility and anti-interference ability.

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CHEMOSPHERE · 2023 · IF 8.8

Effect and mechanism of norfloxacin removal by guava leaf extract in the ZVI/H2O2 system

Baizhou Lu,Zhanqiang Fang,Pokeung Eric Tsang,Jinhua Wu

To overcome the bottlenecks of the conventional zero-valent iron Fenton-like (ZVI/H 2 O 2 ) process, such as low reagent utilization, low applicable pH, and iron sludge contamination, guava leaf extract (GLE) was used as a green promoter to enhance ZVI/H 2 O 2 process in this study. Compared with the ZVI/H 2 O 2 system, the removal rate and k obs of norfloxacin by the ZVI/H 2 O 2 /GLE system were increased by 33.76% and 2.19 times, respectively. The experimental investigation of the mechanism showed that the attack of reactive oxygen species was the main pathway for the removal of pollutants, and three types of reactive oxygen species ( 1 O 2 , O 2 − ,·OH) generations in the ZVI/H 2 O 2 /GLE system were effectively promoted by the introduction of GLE. The reactivity improvement was mainly due to the decrease of pH. At the same time, the chelation of iron ions by GLE promoted the Fe(III)/Fe(II) cycle on the catalyst surface was also a minor mechanism to improve the reactivity. This study provides a crucial reference for the practical application of guava leaf to promote the ZVI/H 2 O 2 process in environmental pollution control .

CAS / MDL: 5470-11-1 66-71-7
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CHEMOSPHERE · 2023 · IF 8.8

Activated carbon filled in a microporous titanium-foam air diffusion electrode for boosting H2O2 accumulation

Fengxia Deng,Shilin Yang,Baojian Jing,Shan Qiu

In the electro-Fenton process, there still suffers concern of low H 2 O 2 generation caused by inadequate mass transfer of oxygen and low selectivity of oxygen reduction reaction (ORR). To solve it, in this study, various particle sizes (850 μm, 150 μm, and 75 μm) of granular activated carbon filled in a microporous titanium-foam substate was used to develop a gas diffusion electrode (AC@Ti–F GDE). This facile-prepared cathode has seen a 176.15% improvement in H 2 O 2 formation compared to the conventional one. Aside from a much higher oxygen mass transfer by creating gas-liquid-solid three-phase interfaces coupled with much high dissolved oxygen, the filled AC played a significant role in H 2 O 2 accumulation. Among these particle sizes of AC, the one in 850 μm has observed the highest H 2 O 2 accumulation, reaching 1487 μM in 2 h electrolysis. Because there is a balance between chemical nature for H 2 O 2 formation and micropore-dominant porous structure for H 2 O 2 decomposition, resulting in an electron transfer of 2.12 and H 2 O 2 selectivity of 96.79% during ORR. In a word, the facial AC@Ti–F GDE configuration is promising for H 2 O 2 accumulation.

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Materials · 2023 ·Vol. 16 ·期 3 ·1261 · IF 3.4

Electrophoretic Deposition of Co3O4 Particles/Reduced Graphene Oxide Composites for Efficient Non-Enzymatic H2O2 Sensing

Qian Wang,Yuzhe Wang,Guiyong Xiao,Xinde Zhu

In this work, the facile fabrication of Co3O4particles/reduced graphene oxide (Co3O4/rGO) composites on Indium tin oxide (ITO) slide was achieved by an electrophoretic deposition and annealing process. The deposition time and ratio of the precursors were optimized. Structural characterization and chemical composition investigation indicated successful loading of Co3O4particles on graphene sheets. When applied as a non-enzymatic H2O2sensor, Co3O4/rGO showed significant electrocatalytic activity, with a wide linear range (0.1–19.5 mM) and high sensitivity (0.2247 mA mM−1cm−2). The good anti-interference ability, reproducibility, and long-term stability of the constructed sensor were also presented. The application of Co3O4/rGO in real sample analysis was evaluated in human urine sample with satisfactory results, indicating the feasibility of the sensor in physiological and medical applications.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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CHEMOSPHERE · 2023 · IF 8.8

Regeneration of methylene blue-saturated biochar by synergistic effect of H2O2 desorption and peroxymonosulfate degradation

Hao Ding,Gongsong Tong,Jingchun Sun,Jiewei Ouyang,Fangge Zhu,Zhi Zhou,Nan Zhou,Mei’e Zhong

Biochar, as an adsorbent, is widely used for the removal of organic pollutants in water body. Hence, after saturated adsorption, regeneration treatment is required to recover the adsorption performance of biochar. In this study, a biochar (P-GBC) prepared by phosphoric acid activation showed high adsorption capacity for methylene blue (MB) with the maximum adsorption capacity (Q m ) of 599.66 mg/g. Then, regeneration treatments using 4 mM peroxymonosulfate (PMS), 0.2 M hydrogen peroxide (H 2 O 2 ) and their mixture were used to regenerate MB-saturated biochar with regeneration efficiencies of 58.24%, 66.01% and 94.88%, respectively. Combining with degradation and quenching experiments, it is found that synergistic effect of H 2 O 2 desorption and PMS degradation is responsible for the enhancement of regeneration efficiency of P-GBC in H 2 O 2 -PMS system and enables a high mineralization rate of 82.68% for the MB adsorbed on P-GBC. Furthermore, EPR tests indicate that singlet oxygen ( 1 O 2 ) is assigned as the primary activate species for the degradation of MB and XPS analyses confirm that graphite nitrogen and carbonyl on P-GBC are the main active sites for the activation of PMS. Compared with conventional regenerants, H 2 O 2 -PMS system has the advantages of low dosage, high mineralization efficiency, and easy accessibility, and is also effective, sustainable and environmentally friendly for the regeneration of organic pollutants-saturated biochar.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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COLLOIDS AND SURFACES B-BIOINTERFACES · 2022 · IF 5.999

H2O2 self-sufficient nanoplatform based on CeO2 QDs decorated MgO2 nanosheet for amplified chemodynamic therapy

Yuyan Yan,Renlu Han,Huijun Zhang,Pengxin Song,Xiangjun Wei,Yafei Hou,Jiancheng Yu,Keqi Tang

Chemodynamic therapy (CDT), which employs Fenton/Fenton-like agents to decompose hydrogen peroxide (H 2 O 2 ) into toxic hydroxyl radical (•OH) to induce cancer cell apoptosis and necrosis, holds great promise in tumor therapy due to its high selectivity . Nevertheless, its efficiency is impaired by the insufficient intracellular H 2 O 2 concentration and/or the insensitive response of Fenton/Fenton-like agents to the slightly acid tumor microenvironment (pH∼7.0–6.5). Herein, we develop a novel CDT reagent based on CeO 2 quantum dot (QD) decorated MgO 2 nanosheets engineered with cascade reactions to boost the intracellular H 2 O 2 level and high pH-activated (pH = 6.5) characteristic for an enhanced CDT. Under the tumor microenvironment (pH = 6.5), MgO 2 nanosheets that are highly reactive can react with H 2 O to produce nontoxic Mg 2+ and abundant H 2 O 2 , boosting the intracellular H 2 O 2 level. The self-generated H 2 O 2 is subsequently converted into •OH by CeO 2 QD, which is served as a relatively high pH-activated (pH = 6.5) Fenton-like agent. The sufficient intracellular H 2 O 2 supply and sensitive response to the slightly acid tumor sites significantly improve the Fenton reaction, leading to the excellent in vivo CDT results with tumor growth inhibition effect. Our work presents a distinctive paradigm for self-boosting CDT efficacy.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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RSC Advances · 2022 ·Vol. 12 ·期 44 ·28349-28358 · IF 4.036

A colorimetric sensing platform for the determination of H2O2 using 2D–1D MoS2-CNT nanozymes

Xin Zhang,Siqin Wang,Jiahao Dao,Jiajing Guo,Yanfang Gao

A novel colorimetric platform based on nano-composites of two-dimensional (2D) molybdenum disulfide nanosheets (MoS2 NSs) and one-dimensional (1D) carbon nanotubes (CNTs), called 2D–1D MoS2-CNT nanozyme, was fabricated for the selective and sensitive determination of hydrogen peroxide (H2O2) in soda water. The MoS2-CNT nanozyme was synthesized through a one-step solvothermal reduction method. The introduced CNTs could effectively prevent the stacking of MoS2 nanosheets (NSs) and not only expanded the interlayer distance of MoS2 NSs from 0.620 nm to 0.710 nm but also improved their specific surface. Under acidic conditions, the as-prepared 2D–1D MoS2-CNT nanozymes could oxidize the colorless 3,3′,5,5′-tetramethylbenzidine (TMB) to blue-oxidized TMB (oxTMB) in the presence of H2O2, resulting in enhanced peroxidase-like (POD-like) activity. The kinetic study showed that MoS2-CNT nanozyme had stronger catalytic activity than natural horseradish peroxidase (HRP). The linear range for H2O2 colorimetric determination was 5.00–500 μmol L−1 with a limit of detection (LOD) of 1.40 μmol L−1. Furthermore, the established determination method was applied to actual samples and the recoveries of H2O2 spiked in soda water were in the range of 92.3–107%, showing feasibility for the analysis of food.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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ACS Catalysis · 2022 · IF 13.7

In Situ Hydroxylation of a Single-Atom Iron Catalyst for Preferential 1O2 Production from H2O2

Bo Sheng,Chaoyuan Deng,Yangfan Li,Shijie Xie,Zhaohui Wang,Hua Sheng,Jincai Zhao

In Fenton or Fenton-like reactions, ·OH obtained by the reductive activation of H2O2 is regarded as the major reactive oxygen species (ROS); however, the generation of other ROS like O2·– and 1O2 cannot be negligible. Since the degradation capability of a certain ROS would be varied to distinctive pollutants, the regulation of ROS production from H2O2 activation should be applicable for a more targeted pollutant degradation. Herein, a series of carbon nitride (C3N4)-supported Fe catalysts with the state of Fe ranging among single-atom, oxide-cluster, and nanoparticle catalysts were fabricated and their activities in photo-Fenton reactions were evaluated. It was uncovered that the single-atom catalyst favored the generation of O2·– and 1O2 via the oxidative activation of H2O2 and the selectivity of 1O2 toward ·OH dynamically increased with the proceeding of H2O2 activation, while the catalysts with an abundance of oxide clusters exhibited a significantly higher conversion of H2O2 to ·OH. In situ FT-IR studies demonstrated that during the H2O2 activation, the single-atom catalyst underwent a more significant surface hydroxylation than the oxide-cluster catalyst. Such a result was further consolidated by the theoretical calculation that the adsorption energy of surface hydroxyl was remarkably higher on the single-atom catalyst. Thereafter, distinctive from the easy desorption of hydroxyl during the reduction of H2O2 to ·OH in oxide-cluster catalysts, the in situ surface hydroxylation on the single-atom catalyst alters the adsorption mode of H2O2 to a H-bonded structure, which steers the selectivity of ROS generation to a more favored oxidative transformation of H2O2 to O2·–/1O2. This work uncovers the decisive role of surface hydroxyl in regulating ROS generation in a heterogeneous Fenton reaction.

CAS / MDL: 93-05-0 9003-99-0
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ULTRASONICS SONOCHEMISTRY · 2022 · IF 9.336

Effects of ultrasound-assisted H2O2 on the solubilization and antioxidant activity of yeast β-glucan

Xia Ma,Lin Dong,Yan He,Shiwen Chen

Yeast β-glucan (YG) possess an extensive range of biological activities, such as the inhibition of oxidation, but the poor water solubility of macromolecular YG limits its application. In this study, through the combined degradation of ultrasonic waves and H 2 O 2 , and the optimization of the main process parameters for solubilizing YG by response surface methodology (RSM), a new product of YG UH was generated. The molecular weight, structural characteristics and degradation kinetics before and after solubilization were evaluated. The results showed that the optimal solubilization conditions were reaction time: 4 h, ultrasonic power: 3 W/mL, H 2 O 2 concentration: 24 %. Under these conditions, ultrasound-assisted H 2 O 2 increased the solubility (from 13.60 % to 70.00 %) and reduced molecular weight (from 6.73 × 10 6 Da to 1.22 × 10 6 Da). Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR), Congo red (CR), scanning electron microscopy (SEM) revealed that ultrasound-assisted H 2 O 2 increased the conformation's flexibility greatly, without changing the main structure of YG. More importantly, solubilization of YG improved free radical scavenging activity with YG UH exhibiting the highest levels of DPPH and ABTS + free radical scavenging activity. These results revealed that ultrasound-assisted H 2 O 2 degradation could be a suitable way to increase the solubility of YG for producing value-added YG.

CAS / MDL: 7722-84-1
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2022 · IF 24.319

Synergistic effect of triphase interface and fluid control for efficient photosynthesis of residue-free H2O2

Huining Huang,Qitao Zhang,Run Shi,Chenliang Su,Yulin Wang,Jiaqi Zhao,Tierui Zhang

Solar-to-chemical energy conversion is a challenging subject for renewable energy storage. Solar-driven hydrogen peroxide (H 2 O 2 ) synthesis is a sustainable and potentially economic technology. Despite great efforts in catalyst engineering, photocatalytic H 2 O 2 production is usually limited by the sluggish oxygen diffusion and H 2 O 2 decomposition side reactions, leading to poor apparent photocatalytic H 2 O 2 production efficiency. Herein, we developed a fluid triphase system that enables both the efficient interfacial oxygen mass transfer and the inhibited H 2 O 2 decomposition side reactions. Such a synergistic effect endowed a residue-free H 2 O 2 production rate of 6.03 μmol h −1 from pure water and oxygen without using any sacrificial agent or additive, with over 120 h continuous irradiation stability. We further designed a photosynthesis-concentration tandem system to produce high concentration H 2 O 2 (10 mM), which demonstrated an effective water disinfection capability as a representative application.

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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2017 · IF 4.233

Supramolecular gels: using an amide-functionalized imidazolium-based surfactant

Ni Cheng,Qi Kang,Jianhong Xiao,Na Du,Li Yu

Studies on supramolecular gel aggregates via supramolecular interactions are very fascinating and impressive. The interactions of gelator with solvent and inorganic salt can functionalize, activate, or control the properties of supramolecular gels. A lot of work on this area has been done, but all these contributions are only at an early stage. In this work, we tuned the gel formation conditions and properties by using low-molecular-weight gelator (LMWGs), amide-functionalized imidazolium-based surfactant , viz., N-cetyl-N′-acetamido imidazolium bromide ([N-C 16 , N′-CONH 2 -Im]Br), in different solvents and with inorganic salt additives. Under chemical (Cu 2+ /H 2 O 2 ) and physical (temperature) stimuli, gel-sol phase transition occurred in the gel formed from 2 wt% [N-C 16 , N′-CONH 2 -Im]Br in the solvent formamide (FM). Accompanied with increased mechanical strength of the gels, morphology alternation from initial straight stripe-shaped structures to curly belt-like textures was observed in the addition of CuBr 2 . From Small-angle X-ray scattering (SAXS) measurements, bilayer units with interdigitated hydrocarbon tails of the gelator were testified to appear in the gels. Comparative experiments demonstrate that the π-π interaction, H-bonding, and hydrophobic interaction between the gelator molecules are the main driving forces for the gelation . The low-cost gelator, facile preparation, and coordination-driven assembly process make the robust gel a good candidate in various applications, such as material templates and drug deliveries.

研究领域: 化学 · 材料科学
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CATALYSIS TODAY · 2021 · IF 6.766

Molecular characteristics of sulfur compounds in oxidative desulfurization for heavy fuel oil based on APPI FT-ICR MS analysis

Jiyuan Fan,Saumitra Saxena,Chengkun Xiao,Jinlin Mei,Gang Wang,Aiping Chen,Wen Zhang,Haidong Li,Aijun Duan,William L. Roberts

Oxidative desulfurization of model oil and heavy fuel oil (HFO) was investigated under mild conditions using H 2 O 2 as an oxidant and acetonitrile as an extractant. The influence factors in the oxidation and extraction processes were evaluated and optimized. The molecular characteristics of the raw feedstock and the desulfurized oils, and the corresponding extraction phases were systematically analyzed by APPI FT-ICR MS, 1 H NMR, etc. The results showed that the desulfurization rate of dibenzothiophene reached 97.7% after 10 min reaction, while the sulfur removal efficiency of HFO was 30.7% under optimized conditions. The structures of sulfur compounds were described in heteroatom type, carbon number distribution vs unsaturation degree. The detected main sulfur-containing compounds are S 1 , S 2 , S 3 , NS, OS, O 2 S, O 2 S 2 , and O 4 S 2 . Based on the APPI FT-ICR MS results, it can be found that almost all the S 1 species have been transformed into sulfone after the oxidation process. Furthermore, the sulfone of O 2 S 1 and O 4 S 2 species in extraction phases were in double bond equivalent (DBE) range from 9 to 25 and carbon number with ≤ 40. 1 H NMR results showed that the α to aromatic CH 3 combined naphthenic CH-CH 2 group accounted for 73.2% in the extraction phase.

研究领域: 化学工程 · 分析化学 · 环境科学
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