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H2O2
PROCESS SAFETY AND ENVIRONMENTAL PROTECTION · 2023 · IF 7.8

Removal of refractory organic compounds from bio-treated landfill leachate using a Fe0-H2O2-MoS2 process under continuous operation mode

Xiaoqin Zhang,Jing Yang,Yueli Chen,Jia Tang,Aiping Zhang

Fe 0 and MoS 2 can synergistically activate H 2 O 2 to generate free radicals for the removal of refractory organic compounds. This study aims to evaluate the Fe 0 -H 2 O 2 -MoS 2 process for the removal of refractory organic compounds from bio-treated landfill leachate (BTL) under continuous operation mode . The results show that the dosage of H 2 O 2 , Fe 0 and MoS 2 all affect the removal effect of the Fe 0 -H 2 O 2 -MoS 2 process on refractory organics during continuous operation. The removal rates of total organic carbon , absorbance at 254 nm and chroma at an initial pH of 3, [H 2 O 2 ] of 5 mM, Fe 0 of 0.4 g/L, MoS 2 of 0.4 g/L and reaction time of 60 min were 65.83%, 85.11% and 93.14%, respectively. The Fe 0 -H 2 O 2 -MoS 2 process can not only effectively destroy the complex structure of refractory organic compounds in the BTL treatment but also reduce the biological toxicity of BTL to a certain extent. In addition, a high organic removal rate can still be maintained during the long-term dynamic reaction process. Therefore, the Fe 0 -H 2 O 2 -MoS 2 process has excellent performance in removing refractory organic compounds from BTL under continuous operation conditions.

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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2023 · IF 9.9

K–N Bridge-Mediated charge separation in hollow g-C3N4 Frameworks: A bifunctional photocatalysts towards efficient H2 and H2O2 production

Xiaoli Jin,Huiqing Wang,Xiongtao Lv,Qing Lan,Teng Ge,Lin Guo,Xin Li,Hongxian Sun,Chenghua Ding,Yuwei Guo,Haiquan Xie,Liqun Ye

The development of bifunctional photocatalysts for enhancing hydrogen (H 2 ) and hydrogen peroxide (H 2 O 2 ) production from water is essential in addressing environmental and energy issues. However, the practical implementation of photocatalytic technology is still constrained by the inadequate separation of photo-generated charge carriers. Herein, potassium (K) atoms are introduced into the interlayers of graphitic carbon nitride (g-C 3 N 4 ) with a hollow hexagonal structure (K-TCN) and are coordinated with N atoms in adjacent layers. The presence of K–N coordination serves as a layer bridge, facilitating the separation of charge carriers. The hollow hexagonal structure reduces the distance over which photogenerated electrons migrate to the surface, thereby enhancing the reaction kinetics. Consequently, the optimized K-TCN exhibits a dramatically improved photocatalytic H 2 (941.6 μmol g −1 h −1 with platinum (Pt) as the cocatalyst) and H 2 O 2 (347.6 μmol g −1 h −1 ) generation as compared to hollow g-C 3 N 4 (TCN) and bulk g-C 3 N 4 nanosheet (CN) without K–N bridge under visible light irradiation. The unique design holds promising potential for developing highly efficient bifunctional photocatalysts towards producing renewable fuels and value-added chemicals.

CAS / MDL: 461-58-5
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APPLIED SURFACE SCIENCE · 2023 · IF 6.7

The complex heterogeneous Fenton reactivity of transition metal-doped ferrihydrite: Insight from the structural variation and pathway of H2O2 activation

Qingru Xie,Yanping Zhu,Haiyang Xian,Qingze Chen,Chengshuai Liu,Fei Wu,Xiaoliang Liang,Runliang Zhu

Doping transition metal into ferrihydrite (Fh) may significantly affect its structure and Fenton reactivity. The comparative study of Fh and M(II)-Fh (M = Cu, Co, or Mn), for the first time, reveals that doping metal ions can alter the property and content of oxygen vacancy (OVs) and the oxidation potential of Fh, which subsequently affects H 2 O 2 decomposition, HO . generation, and Fenton reactivity of the catalysts. The overall Fenton activity of the samples in decomposing bisphenol A decreases in the order Cu-Fh > Fh > Co-Fh > Mn-Fh. In specific, Cu-Fh is the most efficient catalyst as it has the lowest energy barrier for decomposing H 2 O 2 into HO . at OVs sites and the highest oxidation potential (benefiting the reduction of Fe(III) to Fe(II) by H 2 O 2 ). Our findings show the complex heterogeneous Fenton reactivity of M-Fh, and doping can be an efficient strategy for achieving highly efficient Fenton catalysts.

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ChemNanoMat · 2023 ·Vol. 9 ·期 5 ·e202200569 · IF 3.8

A Colorimetric Paper Sensor Based on Self-assembled Nanocomposite Pd−Pt@hemin-rGO/CNTs-COOH for the Detection of H2O2

Yanyu Li,Xiaoyue Zhang,Jinglin Shen,Wei Qi

Graphical A new type of nanocomposite enzymes has been developed, composed of Pd−Pt nanoparticles, hemin-rGO and CNTs-COOH. The nanocomposites show a high peroxidase-like activity and a linear response toward H 2 O 2 in the range of 0.05–500 μM with a determination limit of 0.01 μM. Based on this, a paper sensor was constructed for H 2 O 2 detection in real samples. Nanocomposite enzymes are attracting intensive attention worldwide. In the present study, a novel colorimetric H 2 O 2 paper sensor was developed based on a new type of nanocomposites composed of Pd−Pt nanoparticles, hemin functionalized reduced graphene oxide (hemin-rGO) and carboxylated carbon nanotubes (CNTs-COOH). The proposed nanocomposites show a high peroxidase-like activity. It provides a sensitive platform showing a linear response toward H 2 O 2 in the range of 0.05–500 μM with a determination limit of 0.01 μM. Based on this, the composites were applied to construct a paper sensor for H 2 O 2 detection in real samples. The cost-effectiveness, simplicity and efficiency of this paper sensor could be developed for “point-of-care” analysis and other related areas.

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CHEMICAL ENGINEERING JOURNAL · 2023 · IF 15.1

Bioinspired Jellyfish-like Carbon/Manganese nanomotors with H2O2 and NIR light Dual-propulsion for enhanced tumor penetration and chemodynamic therapy

Yi Xing,Mengyun Zhou,Xiangmei Liu,Minghang Qiao,Liping Zhou,Tailin Xu,Xueji Zhang,Xin Du

Chemodynamic therapy (CDT), which catalyzes the production of highly toxic reactive oxygen species (ROS), has been widely used in tumor therapy in the past five years. However, most of the current nanomaterials for CDT are difficult to penetrate into the tumor effectively due to the lack of motility, resulting in an unsatisfactory CDT effect. Herein, bioinspired jellyfish-like carbon/manganese nanomotors (JCMNs) are designed to achieve hydrogen peroxide (H 2 O 2 ) and NIR light dual-propulsion for the enhanced CDT therapy. Based on the jellyfish-like asymmetric structure, the manganese component can catalyze H 2 O 2 to generate chemical concentration gradient, propelling JCMNs to dynamically generate ROS in cells by self-diffusiophoresis. In addition, the carbon component of JCMNs can absorb near-infrared (NIR) light to produce a temperature gradient, driving JCMNs to enhance tumor penetration by self-thermophoresis. The combination of chemical and NIR light propulsions significantly improves the efficiency of tumor CDT, revealing that it should be a reasonable strategy to promote the development of nanobiomedicine by endowing nanosystems with propulsion capacity.

CAS / MDL: 7722-84-1
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2023 · IF 22.1

Coral-shaped Mn-CuS with hierarchical pores and crystalline defects for high-efficiency H2O2 production via electrocatalytic two-electron reduction

Ao Zhang,Zhongqing Jiang,Shaoda Zhang,Penghua Lan,Naihua Miao,Weiheng Chen,Ning Huang,Xiaoning Tian,Yangjie Liu,Zhongyu Cai

We report the development of non-noble transition metal sulfide catalysts Mn-CuS-x for high-efficiency and selective H 2 O 2 production. In this study, we synthesized Mn-CuS-x with coral-shaped hierarchical porous structure through one-pot hydrothermal reaction. The Mn-CuS-x possesses large specific surface area with plenty of crystalline defects via heteroatom doping of Mn. The Mn-CuS-x kinetically favored 2e − pathway over 4e − pathway, resulting in high selectivity (>92%) to H 2 O 2 production and high H 2 O 2 concentration (∼24.5 mM at 0.6 V vs. RHE) within 3 h for the optimized Mn-CuS-2 catalysts (synthesized with a molar ratio of 1:3:8 (MnCl 2 ·4 H 2 O: CuCl 2 ·2 H 2 O: C 2 H 5 NS)). The Mn-CuS-2 showed excellent stability, indicating that the Mn-CuS electrocatalysts can simultaneously achieve both high stability and enhanced H 2 O 2 production. Our first-principles calculations further confirmed that the heteroatom Mn doping to CuS thermodynamically makes the 2e – -ORR pathway more favorable. This study provides a green, low-cost, and efficient route to produce H 2 O 2 , which is very promising for generating chemicals and liquid fuels.

CAS / MDL: 13454-94-9
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LWT-FOOD SCIENCE AND TECHNOLOGY · 2023 · IF 6

Effects of TiO2 and H2O2 treatments on the biosynthesis of carotenoids and lipids in oleaginous red yeast Rhodotorula glutinis ZHK

Die Zhao,Chunji Li

Microbial carotenoids and lipids are two groups of versatile biomolecules widely used in the food, fuel, pharmaceutical, and cosmetic industries. Rhodotorula glutinis is one of the best-known oleaginous red yeasts that has the remarkable capability to produce an assortment of valuable carotenoids and lipids. Here, the effects of different concentrations of TiO 2 and H 2 O 2 treatments on carotenoid and lipid production in R. glutinis ZHK were investigated. After 120 h of cultivation, the total amount of carotenoids was significantly increased in the TiO 2 (100 mg/L: 23.165 μg/gdw, 750 mg/L: 19.65 μg/gdw) and H 2 O 2 (5 mM: 21.51 μg/gdw, 10 mM: 118.858 μg/gdw) treatments than the control (6.099 μg/gdw). In contrast, as compared to the control, the relative abundance of total lipids was significantly decreased in the TiO 2 (100 mg/L) and H 2 O 2 (10 mM) treatments, respectively. In response to TiO 2 and H 2 O 2 stresses, the increased carotenoids were probably attributed to the down-regulated lipid biosynthesis flux, while the decreased lipids might be ascribed to the down-regulated fatty acid biosynthesis flux. Our results presented herein not only provide an effective strategy for modulating carotenoid and lipid biosynthesis in R. glutinis ZHK but also reveal the molecular foundation to further enhance their bioproductivity by molecular manipulation.

CAS / MDL: 13463-67-7
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TALANTA · 2023 · IF 6.1

Methyl orange as a novel colorimetric iodide indicator with in situ generation of H2O2 by etching uncoated Ag–Ti3C2 nanohybrids

Peng Jin,Wenlong Tan,Xu Li,Jinsong Fan,Kun Li

Iodine intake remains a major public health concern, as both iodine excess and deficiency are related to adverse effects on health. Therefore, developing simple and economical methods to detect I − is still in great demand. Herein, we constructed a visual I − sensing platform based on the uncoated Ag–Ti 3 C 2 nanohybrids using methyl orange (MO) as a colorimetric indicator . Plasmonic nanostructures are frequently employed in colorimetric analysis , but uncoated Ag nanoparticles (NPs) are unstable because their surface energies are usually high. Considering that Ag NPs can be etched by I − via forming Ag–I bond, we introduce Ag–Ti 3 C 2 nanohybrids because uncoated Ag NPs with immaculate surfaces are more conducive to binding with I − and being etched. Dissolved O 2 molecules adsorbed on Ti 3+ of Ti 3 C 2 MXenes enable the in situ generation of H 2 O 2 by iodine-etching of uncoated Ag–Ti 3 C 2 nanohybrids. ∙OH radicals promote the degradation of MO through a self-driven Fenton-like process, exhibiting the color variation from orange to transparent. Under optimal conditions, the absorbance of MO at 465 nm decreases linearly with the concentration of I − in the range of 0.5–300 μM, with a limit of detection as low as 0.31 μM. This work opens the feasibility of iodine-etching of Ag in developing novel probes for facile colorimetric determination of I − .

CAS / MDL: 7789-24-4
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ANALYTICAL CHEMISTRY · 2022 · IF 8.008

Atomic Dispersion of Zn2+ on N-Doped Carbon Materials: From Non-Activity to High Activity for Catalyzing Luminol-H2O2 Chemiluminescence

Jing Lei,Xiaoqing Sun,Yan Jin,Chunli Xu,Baoxin Li

Fe and Co single-atom catalysts (SACs) have been widely explored in many fields, while Zn SACs are still in their infancy stage. Herein, we unexpectedly found that atomically dispersed Zn2+ on N-doped carbon material (Zn-N-C) exhibited high catalytic activity on luminol-H2O2 chemiluminescence (CL) reaction. The Zn-N-C SACs were readily prepared through simple pyrolyzation of the cheap precursors (dopamine and ZnCl2). The mechanism of Zn SAC-catalyzed CL reaction of luminol-H2O2 was investigated in detail. The activity of Zn SACs originated from the Zn-N sites in the Zn-N-C structure. The monoatomic dispersion makes Zn2+ catalytic performance change from no activity to high activity in luminol-H2O2 CL reaction. This study demonstrated the particularity of the monatomic metal catalyst over the conventional metal ion. This work provides the unprecedented perspective for design of new metal SACs in CL reaction.

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Acta Biomaterialia · 2022 · IF 10.633

H2O2-triggered “off/on signal” nanoparticles target P-selectin for the non-invasive and contrast-enhanced theranostics for arterial thrombosis

Ying Wang,Chuanjiang Jian,Yiqing Long,Xiaowen Xu,Yang Song,Zongning Yin

Pathological coagulation within an injured artery and the subsequent cardiovascular complications, such as stroke and heart attack, greatly threaten human life. Inspired by the biochemical features of acute arterial thrombosis, such as abundant activated platelets and hydrogen peroxide (H 2 O 2 ), we constructed platelet-targeted theranostic nanoparticles (CyBA/PFM NPs) with H 2 O 2 -triggered photoacoustic contrast enhancement and antithrombotic capabilities. CyBA/PFM NPs were designed to target platelet-rich clots via fucoidan segment within the carrier, which could be activated by H 2 O 2 to produce fluorescent “CyOH” molecules, thus turning on the photoacoustic signal. CyBA/PFM NPs showed obvious amplification of fluorescence following incubation with fresh clots, exhibiting efficient scavenging ability of intracellular reactive oxygen species (ROS). In a FeCl 3 -induced mouse model of carotid thrombosis, CyBA/PFM NPs significantly amplified the photoacoustic contrast in thrombogenic tissues, effectively eliminated ROS within the occlusion site, and suppressed the thrombus formation , accompanied by a normalization of the soluble CD40L level. Given their accurate imaging potential, potent antithrombotic activities and acceptable biosafety, CyBA/PFM NPs hold strong potential as nanoscale theranostics for H 2 O 2 -correlated cardiovascular diseases. Statement of significance In this study, we developed a platelet-targeted and H 2 O 2 -triggered nanosystem self-assembled from phenylboronated fucoidan/maltodextrin polymers and responsive near-infrared probes. The fucoidan segment within the carrier could facilitate the specific delivery of the therapeutic polymers and probes to the platelet-rich arterial thrombus. In a mouse model of FeCl 3 -induced arterial thrombosis, the system could be activated by H 2 O 2 to produce fluorescent “CyOH” molecules, thus turning on the photoacoustic signal and specifically imaging thrombosed tissues. Besides, CyBA/PFM NPs significantly effectively eliminated ROS within the occlusion site and suppressed the thrombus formation. Given their theranostic potential and acceptable biosafety, this system has great potential for H 2 O 2 -correlated cardiovascular diseases.

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JOURNAL OF HAZARDOUS MATERIALS · 2023 · IF 13.6

Highly selective electrosynthesis of H2O2 by N, O co-doped graphite nanosheets for efficient electro-Fenton degradation of p-nitrophenol

Fangmin Wu,Jun Nan,Tianzuo Wang,Zhencheng Ge,Bohan Liu,Meng Chen,Xuesong Ye

The activity and selectivity of the cathode towards electrosynthesis of H 2 O 2 are critical for electro-Fenton process. Herein, nickel-foam modified with N, O co-doped graphite nanosheets (NO-GNSs/Ni-F) was developed as a cathode for highly efficient and selective electrosynthesis of H 2 O 2 . Expectedly, the accumulation of H 2 O 2 at pH= 3 reached 494.2 mg L −1 h −1 , with the selectivity toward H 2 O 2 generation reaching 93.0%. The synergistic effect of different oxygen-containing functional groups and N species on the performance and selectivity of H 2 O 2 electrosynthesis was investigated by density functional theory calculations, and the combination of epoxy and graphitic N (EP + N) was identified as the most favorable configuration with the lowest theoretical overpotential for H 2 O 2 generation. Moreover, NO-GNSs/Ni-F was applied in the electro-Fenton process for p-nitrophenol degradation, resulting in 100% removal within 15 min with the kinetic rate constant of 0.446 min −1 and 97.6% mineralization within 6 h. The efficient removal was mainly attributed to the generation of bulk ·OH. Furthermore, NO-GNSs/Ni-F exhibited excellent stability. This work provides a workable option for the enhancement of H 2 O 2 accumulation and the efficient degradation of pollutants in electro-Fenton system.

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SCIENCE OF THE TOTAL ENVIRONMENT · 2023 · IF 9.8

Tungsten disulfide (WS2) is a highly active co-catalyst in Fe(III)/H2O2 Fenton-like reactions for efficient acetaminophen degradation

Dongqin He,Dongli Wang,Hongwei Luo,Yifeng Zeng,Ganning Zeng,Jun Li,Xiangliang Pan

The most important factor that restricts the decomposition of H 2 O 2 in the Fe 3+ /H 2 O 2 reaction is the slow cycling efficiency of reducing Fe 3+ to Fe 2+ . In this study, the addition of tungsten disulfide (WS 2 ) as a co-catalyst achieved a rapid cycling of the reaction rate-limiting step and a significant enhancement of H 2 O 2 decomposition, which resulted in the effective degradation of acetaminophen (APAP). Results show that 99.6% of APAP (5 mg L −1 ) could be degraded by H 2 O 2 /Fe 3+ /WS 2 system within 2.5 min. The conversion of Fe 3+ to Fe 2+ occurred mainly on the surface of WS 2 due to the redox reaction of the exposed W 4+ active sites with Fe 3+ after the unsaturated S atoms were bound to protons. Electron paramagnetic resonance (EPR) and radical quenching experiments evaluated the contribution of hydroxyl radical (•OH) and superoxide radical (O 2 • − ) in the degradation of pollutants. WS 2 showed good recoverability after four cycles of the reaction. This study provides a new perspective to improve the efficiency of Fe 3+ /H 2 O 2 and provides a reference for the involvement of transition metal sulfides in advanced oxidation processes (AOPs).

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