Catalytic Decomposition Of H2O2 Research Articles

Facile Synthesis of Copper Telluride Nanoparticles as a Robust Nanoenzymatic Catalyst for Intrinsic Peroxidase‐Like Activity

AbstractCopper telluride nanoparticles are classified as the family of metal chalcogenides and were synthesized using a simple solvothermal method using a new source of telluride, ditelluride diphenyl. The characterized techniques revealed that the atomic composition of copper tellurides is Cu2Te and particles are spherical. This study is greatly examined by different designed experiments for the proof of the intrinsic peroxidase‐like activity of copper telluride nanoparticles and its effectiveness in a variety of similar structures. Cu2Te nanoparticles can convert peroxidase substrates (TMB and OPD) to colored products in the presence of H2O2. In addition, the as‐prepared nanoparticles have the potential to oxidize DPPH and ABTS substrates. Michaelis–Menten constant KM value for TMB and H2O2 was found to be 12 mM and 0.60 mM for H2O2 and the Vmax value of the Cu2Te was found to be TMB and H2O2 was 2.50×10−7 and 0.82×10−8 MS−1. These data are found to be almost comparable with natural peroxidase HRP and other artificial enzymes reported in the literature. The natural peroxidase‐like activities of Cu2Te nanoparticles originated from the catalytic decomposition of H2O2 into ⋅OH radical, which was confirmed from the ESR spin‐trapping technique and using a fluorescence probe, terephthalic acid.

L-Cysteine-Tuned the Hierarchical Structure Based on Benzimidazole: Synthesis, Characterization, and Application in Ratiometric Electrochemiluminescence Immunoassay.

Efficient and robust electrochemiluminescence (ECL) emitters are crucial for enhancing the ECL immunosensor sensitivity. This study introduces a novel ECL emitter, CoBIM/Cys, featuring a hierarchical core-shell structure. The core of the structure is created through the swift coordination between the sulfhydryl and carboxyl groups of l-cysteine (l-Cys) and cobalt ions (Co2+), while the shell is constructed by sequentially coordinating benzimidazole (BIM) with Co2+. This design yields a greater specific surface area and a more intricate porous structure compared to CoBIM, markedly enhancing mass transfer and luminophore accessibility. Moreover, the l-Cys and Co2+ core introduces Co-S and Co-O catalytic sites, which improve the catalytic decomposition of H2O2, leading to an increased production of hydroperoxyl radicals (OOH•). This mechanism substantially amplifies the ECL performance. Leveraging the competitive interaction between isoluminol and BIM for OOH• during ECL emission, we developed a ratiometric immunosensor for cardiac troponin I (cTnI) detection. This immunosensor demonstrates a remarkably broad detection range (1 pg mL-1 to 10 ng mL-1), a low detection limit (0.4 pg mL-1), and exceptional reproducibility and specificity.

Silver doped anatase nanocomposite: a novel photocatalyst with advanced activity under visible light for waste-water treatment

Anatase is a universal semiconductor photocatalyst; however, its wide band-gap energy limits its entire solar spectrum absorption to only 5%. Anatase could be activated in the visible region via nobel metal deposition. This study reports on the facile synthesis of colloidal mono-dispersed anatase nanoparticles of 5 nm particle size via hydrothermal synthesis. Nobel metals (Silver, Nickel) were deposited on colloidal anatase surface. The photocatalytic activities of Ag–TiO2, and Ni–TiO2 were investigated for the degradation of basic fuchsin dye. Ag–TiO2 nanocomposite demonstrated enhanced adsorption activity in dark, as well as superior photocatalytic. Ag–TiO2 nanocomposite demonstrated enhanced removal efficiency by 70.8% under visible irradiation to virgin anatase. Ag–TiO2 nanocomposite demonstrated enhanced oxygen-lattice with low binding energy using XPS analysis. Ag–TiO2 experienced band gap energy of 2.35 eV compared with 3.2 eV for virgin anatase; this feature could secure enhanced solar absorption. Ag–TiO2 demonstrated excellent photo-degradation efficiency of 88% with 0.3% H2O2 under visible light. Deposited silver could catalyze H2O2 decomposition and could promote free radical generation; Ag–TiO2 nanocomposite is a promising photocatalyst for wastewater treatment applications.

Single Atom Catalysts Remodel Tumor Microenvironment for Augmented Sonodynamic Immunotherapy.

The immunosuppressive tumor microenvironment (TME) is a huge hurdle in immunotherapy. Sono-immunotherapy is a new treatment modality that can reverse immunosuppressive TME, but the sonodynamic effects are compromised by overexpressed glutathione (GSH) and hypoxia in the TME. Herein, this work reports a new sono-immunotherapy strategy using Pdδ+ single atom catalysts to enhance positive sonodynamic responses to the immunosuppressive and sono-suppressive TME. To demonstrate this technique, this work employs rich and reductive Ti vacancies in Ti3-xC2Ty nanosheets to construct the atomically dispersed Pd-C3 single atom catalysts (SAC) with Pd content up to 2.5 wt% (PdSA/Ti3-xC2Ty). Compared with Pd nanoparticle loaded Ti3-xC2Ty, PdSA/Ti3-xC2Ty single-atom enzyme showed augmented sonodynamic effects that are ascribed to SAC facilitated electron-hole separation, rapid depletion of overexpressed GSH by ultrasound (US) excited holes, and catalytic decomposition of endogenous H2O2 for relieving hypoxia. Importantly, the sono-immunotherapy strategy can boost abscopal antitumor immune responses by driving maturation of dendritic cells and polarization of tumor-associated macrophages into the antitumoral M1 phenotype. Bilateral tumor models demonstrate the complete eradication of localized tumors and enhance metastatic regression. Th strategy highlights the potential of single-atom catalysts for robust sono-immunotherapy by remodeling the tumor microenvironment.

Double-enhanced sandwich electrochemiluminescence aptasensor based on g-C3N4–Au-luminol nanocomposites and ZnCuS nanosheets for highly sensitive detection of mucin 1

The traditional luminol electrochemiluminescence (ECL) sensing suffers from low signal response and instability issues. Here, an Au/ZnCuS double-enhanced g-C3N4-supported luminol ECL aptasensor is constructed for the sensitive detection of human mucin 1 (MUC1). In this platform, g-C3N4 of a large specific surface area is beneficial to load more luminol illuminants. Au nanoparticles promote the decomposition of H2O2 coreactants to generate more reactive oxygen (•OH and O2•−) intermediates, while ZnCuS can immobilize the aptamer and simultaneously catalyze H2O2 decomposition, realizing the double-wing signal amplification. Under optimal conditions, this sensor shows a good detection capability within 1.0 × 10−4–1.0 × 103 ng mL−1 and a low detection limit of 5.0 × 10−5 ng mL−1, as well as ideal stability, selectivity, and reproducibility. This double-enhanced aptasensor highlights a new signal-enhancement approach for early biomarker detection.

Enhancing Cu-EDTA decomplexation in a discharge plasma system coupled with nanospace confined iron oxide: Insights into electron transfer and high-valent iron species

Decomplexation of heavy metal-organic complexes dominated by reactive oxygen species (ROS) oxidation had attracted extensive attention. Nanospace confinement is a novel strategy to enhance pollutant removal due to its regulation on ROS transformation and local accelerated dynamics. Herein, nano-confined Fe2O3 catalyst supported by carbon nanotubes (Fe2O3-in-CNTs) was synthesized, and it displayed obvious synergistic effects on decomplexation of Cu-EDTA complex in a non-thermal plasma (NTP) process. Cu-EDTA decomplexation efficiency reached 98.8% within 20 min in the NTP/Fe2O3-in-CNTs system, and the corresponding kinetic constant was 4.5 and 2.5 times as that in single NTP and unconfined systems, respectively. Based on experimental and theoretical results, nanospace confinement induced electron localization around Fe and C atoms and rearrangement of orbital electrons, favoring strongly oxidative FeⅣ formation and catalytic decomposition of H2O2 and O3. Nanospace confinement made Cu-EDTA decomplexation process transform from radical pathway to non-radical pathway. Cu-EDTA decomplexation pathways in the NTP/Fe2O3-in-CNTs were proposed.

Biodegradable CoSnO3 nanozymes modulate pH-responsive graphene quantum dot release for synergistic chemo-sonodynamic-nanocatalytic cancer therapy

Albeit nanozymes are widely applied for nanocatalytic therapy (NCT), the unsatisfactory catalytic activity of nanozymes accompanied by complex tumor microenvironment (TME) greatly pose a barrier to the therapeutic effect of NCT. Moreover, developing a high-efficiency nanozyme with biodegradability is still a huge challenge, which hinders their further clinical translation. Herein, pH-responsive biodegradable CoSnO3 nanocubes are synthesized and employed as sonosensitizers and nanozymes due to their narrow bandgaps (1.6 eV) and Co2+/Sn4+-mediated multi-enzyme activities. After depositing the graphene quantum dot (GQD) topoisomerase inhibitors on CoSnO3 nanocubes, the heterojunction-fabricated GQD/CoSnO3 shows cascaded amplification of ROS generation, which is ascribed to the inhibition of electron-hole pair recombination, Co2+-mediated peroxidase (POD)-mimic catalytic reaction to generate OH, Co3+/Sn4+-mediated depletion of overexpressed GSH, and catalytic decomposition of endogenous H2O2 for providing more O2 for enhanced SDT. More importantly, GQD/CoSnO3 heterojunctions are slowly degraded in the weakly acidic TME, resulting the tumor-specific release of GQDs after completion of SDT, which could induce DNA damage and cell apoptosis for chemotherapy to further enhanced the antitumor efficacy. The synergetic therapeutic efficacy of GQD/CoSnO3 heterojunctions through chemotherapy, SDT, and NCT could realize “three-in-one” multimodal oncotherapy to completely eliminate tumors without recurrence. This work provides a paradigm of exploring pH-responsive biodegradable nanozymes as a drug carrier to realize tumor-specific drug release for enhanced SDT and NCT.

An NIR-II-photoresponsive CoSnO3 nanozyme for mild photothermally augmented nanocatalytic cancer therapy.

The main challenges of nanozyme-based tumor catalytic therapy (NCT) lie in the unsatisfactory catalytic activity accompanied by a complex tumor microenvironment (TME). A few nanozymes have been designed to possess both enzyme-like catalytic activities and photothermal properties; however, the previously reported nanozymes mainly utilize the inefficient and unsafe NIR-I laser, which has a low maximum permissible exposure limit and a limited penetration depth. Herein, we report for the first time an all-in-one strategy to realize mild NIR-II photothermally amplified NCT by synthesizing amorphous CoSnO3 nanocubes with efficient triple enzyme-like catalytic activities and photothermal conversion properties. The presence of Co2+ and Sn4+ endows CoSnO3 nanocubes with the triple enzyme-like catalytic activities, not only achieving enhanced reactive oxygen species (ROS) generation through the Co2+-mediated peroxidase-like catalytic reaction to generate ˙OH and Sn4+-mediated depletion of overexpressed GSH, but also realizing the catalytic decomposition of endogenous H2O2 for relieving tumor hypoxia. More importantly, the obtained CoSnO3 nanocubes with a high photothermal conversion efficiency of 82.1% at 1064 nm could achieve mild hyperthermia (43 °C), which further improves the triple enzyme-like catalytic activities of the CoSnO3 nanozyme. The synergetic therapeutic efficacy of the NIR-II-responsive CoSnO3 nanozyme through mild NIR-II PTT-enhanced NCT could realize all-in-one multimodal tumor therapy to completely eliminate tumors without recurrence. This study will open a new avenue to explore NIR-II-photoresponsive nanozymes for efficient tumor therapy.

PH-responsive iron-loaded carbonaceous nanoparticles for chemodynamic therapy based on the Fenton reaction.

The Fenton reaction-based chemodynamic therapy is a form of cancer therapy, and its efficacy can be significantly improved by promoting catalytic reactions involving iron ions. A system with high catalytic capacity and low biological toxicity that effectively inhibits tumor progression is required for optimal treatment. In this study, iron-loaded carbonaceous nanoparticles (CNPs@Fe) with Fenton catalytic activity were fabricated and applied for the chemodynamic therapy of cancer. The carbonaceous nanoparticles derived from glucose via a caramelization reaction demonstrated high biocompatibility. Besides, aromatic structures in the carbonaceous nanoparticles helped accelerate electron transfer to enhance the catalytic decomposition of H2O2, resulting in the formation of highly reactive hydroxyl radicals (˙OH). At pH 6.0 (representing weak acidity in the tumor microenvironment), the Fenton catalytic activity of CNPs@Fe in the decomposition of H2O2 was 15.3 times higher than that of Fe2+ and 28.3 times higher than that of Fe3O4via a chromogenic reaction. The reasons for the enhancement were revealed by analyzing the chemical composition of carbonaceous nanoparticles using high-resolution mass spectra. The developed Fenton agent also demonstrated significant therapeutic effectiveness and minimal side effects in in vitro and in vivo anticancer studies. This work proposes a novel approach to promote the generation of reactive oxygen species (ROS) for the chemodynamic therapy of cancer.

Enhanced in situ production of Fenton reagent's by nanobubble aeration and sacrificial iron anodes in the electro-Fenton process

Wastewater treatment is currently focused on the development of simple, safe, cost-effective technologies for the complete destruction of persistent organic pollutants. A novel reagent-free electro-Fenton process by integrated nano-bubble aeration and sacrificial iron anode is proposed, which improves mass transferability of large content dissolved oxygen (10.55mgL−1) in the electrolyte and then quickly transported oxygen to the electrode surface. The synergistic effect of nanobubble aeration and sacrificial iron anodes can product a highly efficient hydrogen peroxide (H2O2) (310 mgL−1) and enhanced electrochemically driven reduction of Fe2+ at pH 3.5 and current density 55 mAcm−2. The degradation of phenol (100 mgL−1) with hydroxyl radicals (⋅OH) generated in situ is described by a pseudo first-order kinetics mode and was fast (0.036 min−1), which obtained a remarkable decolorization of over 58.7 % in 60 min. With nanobubble aeration and sacrificial iron anode, the catalytic decomposition of H2O2 to ⋅OH by Fe2+ was more powerful, achieving a cost-effective and green design without reagents.

In Situ Synthesis of Ru/TiO2- x @TiCN Ternary Heterojunctions for Enhanced Sonodynamic and Nanocatalytic Cancer Therapy.

Albeit nanozymes-based tumor catalytic therapy (NCT) relies on endogenous chemical reactions that could achieve tumor microenvironment (TME)-specialized reactive oxygen species (ROS) production, the unsatisfactory catalytic activity of nanozymes accompanied by complex TME poses a barrier to the therapeutic effect of NCT. Herein, a one-step in situ synthesis strategy is reported to construct ternary Ru/TiO2- x @TiCN heterojunctions through oxidative conversion of TiCN nanosheets (NSs) to TiO2- x NSs and reductive deposition of Ru3+ to Ru nanoparticles. The narrow bandgap and existence of heterojunctions enhance the ultrasound-activated ROS generation of Ru/TiO2- x @TiCN because of the accelerated electron transfer and inhibits electron-hole pair recombination. The augmented ROS production efficiency is achieved by Ru/TiO2- x @TiCN with triple enzyme-like activities, which amplifies the ROS levels in a cascade manner through the catalytic decomposition of endogenous H2 O2 to relieve hypoxia and heterojunction-mediated NCT, as well as depletion of overexpressed glutathione. The satisfactory therapeutic effects of Ru/TiO2- x @TiCN heterojunctions are achieved through synergetic sonodynamic therapy and NCT, which achieve the complete elimination of tumors without recurrence. This strategy highlights the potential of in situ synthesis of semiconductor heterojunctions as enhanced sonosensitizers and nanozymes for efficient tumor therapy.

Efficient removal of aromatic pollutants via catalytic wet peroxide oxidation over synthetic anisotropic ilmenite/carbon nanocomposites

As one of the most common ferrous (Fe2+)-containing oxide minerals in the Earth’s crust, ilmenite (FeTiO3) is a potential low-cost heterogeneous Fenton-like catalyst for organic wastewater treatment via catalytic wet peroxide oxidation (CWPO). However, it suffers from low activity and long induction time. Herein anisotropic FeTiO3/C nanocomposite with rich Fe2+ ions on large surface area of 159.0 m2 g−1 (surface Fe/Ti and Fe2+/Fe3+ ratios were respectively 2.1 and 2.0) was prepared via cetyltrimethylammonium (CTA+)-assisted sol-gel synthesis. CTA+ modulated the growth of FeTiO3 nanoparticles with more exposed metallic sites by preferential adsorption on its (104) plane via electrostatic attraction, provided the carbon source and facilitated the generation of more Fe2+ ions at the interface of FeTiO3/C via carbothermal reduction of FeTiO3. FeTiO3/C efficiently catalyzed CWPO removal of six aromatic pollutants with different charges (25 mg L−1 each) at 25 oC and pH 3.0 without an induction period owing to rich Fe2+ content on neutral surface (pHpzc ~3.3)—three dye solutions completely decolorized in 1 h and three antibiotics degraded by >90% in 3 h. Reusability of FeTiO3/C was demonstrated with cationic rhodamine B and anionic orange G dyes in five consecutive runs. Scavenging tests and spin-trapping EPR spectra confirmed the generation of dominant ·OH and minor O2•− species for organic degradation via catalytic decomposition of H2O2 on FeTiO3/C as a heterogeneous Fenton-like catalyst.

Label-Free Imaging of Catalytic H2O2 Decomposition on Single Colloidal Pt Nanoparticles Using Nanofluidic Scattering Microscopy.

Single-particle catalysis aims at determining factors that dictate the nanoparticle activity and selectivity. Existing methods often use fluorescent model reactions at low reactant concentrations, operate at low pressures, or rely on plasmonic enhancement effects. Hence, methods to measure single-nanoparticle activity under technically relevant conditions and without fluorescence or other enhancement mechanisms are still lacking. Here, we introduce nanofluidic scattering microscopy of catalytic reactions on single colloidal nanoparticles trapped inside nanofluidic channels to fill this gap. By detecting minuscule refractive index changes in a liquid flushed trough a nanochannel, we demonstrate that local H2O2 concentration changes in water can be accurately measured. Applying this principle, we analyze the H2O2 concentration profiles adjacent to single colloidal Pt nanoparticles during catalytic H2O2 decomposition into O2 and H2O and derive the particles' individual turnover frequencies from the growth rate of the O2 gas bubbles formed in their respective nanochannel during reaction.

An electrochemical sensor based on FeCo bimetallic single-atom nanozyme for sensitive detection of H2O2

Efficient catalytic decomposition of H2O2 is accompanied by electron transfer through Fe-Nx active sites of hemin in the human body. Inspired by this reaction process, the Fe SAs/Co CNs were successfully synthesized by combined Co atomic sites with nitrogen-carbon doped Fe single-atom active sites (SAs). The synergy between transition metals not only reduces agglomeration during synthesis but also improves its own electrical conductivity due to the interaction between Fe and Co that promotes the formation of graphite surface. Crucially, the synergistic effect of the Co site significantly enhanced the peroxidase activity of the Fe SAs and the reaction rate of the Fenton-like reaction, resulting in an efficient detection of H2O2. Catalytic kinetic calculations and enzymatic kinetic calculations were used to verify the electron transfer rate and catalytic performance of their constructed electrochemical sensing interfaces. The results showed that Fe SAs/Co CNs@GCE showed better detection performance than Fe SAs CNs@GCE. It was applied successfully to detect H2O2 released from cells in real-time as well. The linear detection range of Fe SAs/Co CNs@GCE for H2O2 was 1–16664 μM, and the detection limit was as low as 0.25 μM. Furthermore, an electrochemical sensing chip was constructed using Fe SAs/Co CNs@SPE and the prepared microfluidic channel. The constructed portable FeSAs/Co CNs@SPE had a linear range of 1–400 μM and a detection limit of 0.36 μM and achieved the recovery detection of H2O2 in serum. The electrochemical sensing interfaces constructed based on Fe SAs/Co CNs all have efficient catalytic performance and excellent real-time hydrogen peroxide detection performance, which have practical application potential for human oxidative stress level detection. And it provides a novel approach to the trace detection of bioactive small molecules.

Functional Nanozymes Consisting of Co2+‐ZIF‐67 Metal‐Organic Framework Nanoparticles and Co2+‐ZIF‐67/Polyaniline Conjugates

AbstractCo2+‐ZIF‐67 metal‐organic framework nanoparticles (NMOFs), act as nanozymes catalyzing diverse processes, including peroxidase, oxidase, and catalase activities. Peroxidase activities are reflected by the nanozyme‐catalyzed H2O2 oxidation of dopamine to aminochrome, the H2O2 oxidation of NADH to NAD+, the H2O2‐catalyzed generation of chemiluminescence through oxidation of luminol, and the H2O2‐mediated oxidation of aniline to polyaniline. Oxidase activities of the nanozyme are demonstrated by the Co2+‐ZIF‐67 NMOFs catalyzed aerobic oxidation of dopamine to aminochrome and of NADH to NAD+, and catalase activities of the nanozyme are reflected by the catalytic decomposition of H2O2. Moreover, the Co2+‐ZIF‐67 catalyzed oxidation of aniline to polyaniline (PAN) by H2O2 is accompanied by the coating of NMOFs with PAN to yield a Co2+‐ZIF‐67/PAN hybrid material. Coating the particles in the presence of guest substrates leads to molecular imprinted PAN matrices revealing enhanced ZIF‐67 catalyzed transformations as compared to non‐imprinted PAN matrices. This is demonstrated by imprinting of 2,2′‐azinobis(3‐ethylbenzothiazoline‐6‐sulfonic acid), ABTS2−, in the PAN coating and the 3.3‐fold enhanced catalyzed oxidation of ABTS2− by H2O2, as compared to the non‐imprinted PAN hybrid composite. Moreover, imprinting of L‐/D‐DOPA in the PAN coating of Co2+‐ZIF‐67 NMOFs leads to chiro‐selective H2O2‐guided oxidation of L‐/D‐DOPA to dopachrome by the NMOFs/PAN composite.

Green synthesis of silver nanoparticles using durian rind extract and optical characteristics of surface plasmon resonance-based optical sensor for the detection of hydrogen peroxide

Abstract Silver nanoparticles (AgNPs) have been efficaciously synthesized from AgNO3 via an easy and green method, also called green synthesis, using Mon Thong durian (Durio zibethinus L.) rind extract. The inner shell of durian rind extract was used as an intermediary for the synthesis of AgNPs because the absorption spectra of the AgNP colloid extracted from the inner shell had a higher absorption than that of the outer shell. Additionally, we have found more fructose and glucose – which act as a reducing agent – and protein and carbohydrates – which act as the stabilizer – in a higher amount in the inner shell than the extract from the outer shell. The synthesized AgNPs were mainly spherical in shape and exhibited a relatively narrow size distribution with an average particle diameter of 10.2 ± 0.2 nm. In the reduction of hydrogen peroxide (H2O2), these nanoparticles demonstrate catalytic activity. The degradation of AgNPs, including the catalytic decomposition of H2O2, causes a considerable change in the absorbance strength of the surface plasmon resonance band depending on the H2O2 concentration. Over a broad concentration range of 10−1–10−6 mol·L−1 H2O2, a good sensitivity and a linear response are achieved. This sensor’s quantification limit is found to be 0.9 µmol·L−1 H2O2. Therefore, this optical sensor for the detection of H2O2 can be potentially applied in the determination of color indicators in medical or clinical diagnosis, biochemical analysis, and environmental applications.

Intrinsic peroxidase-like activity of dissolved black carbon released from biochar

Dissolved black carbon (DBC) is an important constituent of the natural organic carbon pool, influencing the global carbon cycling and the fate processes of many pollutants. In this work, we discovered that DBC released from biochar has intrinsic peroxidase-like activity. DBC samples were derived from four biomass stocks, including corn, peanut, rice, and sorghum straws. All DBC samples catalyze H2O2 decomposition into hydroxyl radicals, as determined by the electron paramagnetic resonance and the molecular probe. Similar to enzymes that exhibit saturation kinetics, the steady-state reaction rates follow the Michaelis−Menten equation. The peroxidase-like activity of DBC is controlled by the ping-pong mechanism, as suggested by parallel Lineweaver−Burk plots. Its activity increases with temperature from 10 to 80 °C and has an optimum at pH 5. The peroxidase-like activity of DBC is positively correlated with its aromaticity as aromatics can stabilize the reactive intermediates. The active sites in DBC also involve oxygen-containing groups, as inferred by increased activity after the chemical reduction of carbonyls. The peroxidase-like activity of DBC has significant implications for biogeochemical processing of carbon and potential health and ecological impacts of black carbon. It also highlights the need to advance the understanding of the occurrence and role of organic catalysts in natural systems.

Catalytic Decomposition of H2O2 in the Aqueous Dispersions of the Potassium Polytitanates Produced in Different Conditions of Molten Salt Synthesis.

It is shown that the potassium polytitanate powder (PPT) synthesized at 500 °C via the treatment of powdered TiO2 (rutile) in molten mixtures of KOH and KNO3 is a cheap and effective catalyst of H2O2 chemical decomposition in aqueous solutions. At the same time, the PPT catalytic activity strongly depends on the [TiO2]:[KOH]:[KNO3] weight ratio in the mixture used for the synthesis, increasing with [KNO3] in the order of PPT (30:30:40) < PPT (30:50:20) < PPT (30:70:0). The obtained results are explained by increased [Ti3+] in the PPT structure (XPS data), which is grown in this order from 0 to 4.0 and 21.9 at.%, respectively, due to the reduced oxidation activity of the melt used for PPT synthesis. The mechanism of the autocatalytic process taking place in the PPT-H2O2-H2O system is analyzed. Taking into account the data of FT-IR spectroscopy, it is assumed that the increased catalytic activity of the investigated materials is related to the increased surface concentration of the Ti4+-O(H)-Ti4+ groups, formed from the Ti3+-O(H3O+)-Ti4+ clusters and further transformed into Ti-O-O-H catalytic centers. Some possible applications of the PPT-H2O2-H2O catalytic system, including the oxidation processes of green chemistry and photo-catalysis, are discussed.

Oxygen-induced dual-signal point-of-care testing aptasensor for aflatoxin B1 detection using platinum nanoparticle catalysis in visual fluorometry and gravimetry

Point-of-care testing (POCT) has experienced rapid development owing to its advantages of rapid testing, low cost and strong operability, making it indispensable for analyte detection in outdoor or rural areas. In this study, we propose a novel method for the detection of aflatoxin B1 (AFB1) using a dual-signal readout approach within a unified system. This method employs dual channel modes, namely visual fluorescence and weight measurements, as the signal readouts. Specifically, a pressure-sensitive material is utilized as a visual fluorescent agent, its signal can be quenched in the presence of high oxygen pressure. Additionally, an electronic balance, commonly used for weight measurement, is adopted as another signal device, where the signal is generated through the catalytic decomposition of H2O2 by platinum nanoparticles. The experimental results demonstrate that the proposed device enables accurate AFB1 detection within the concentration range of 1.5–32 μg mL−1, with a detection limit of 0.47 μg mL−1. Moreover, this method has been successfully applied for practical AFB1 detection with satisfactory results. Notably, this study pioneers the use of a pressure-sensitive material as a visual signal in POCT. By addressing the limitations of single-signal readout approaches, our method fulfills requirements of intuitiveness, sensitivity, quantitative analysis and reusability.

Novel Application of MnO2–H2O2 System for Highly Efficient Arsenic Adsorption and Oxidation

A novel manganese dioxide–hydrogen peroxide (MnO2–H2O2) system was developed for effective Arsenic (As) removal. Under the specified conditions of no external mechanical stirring, a trace H2O2 concentration of 0.015 wt%, and a MnO2 concentration of 25 mg/L, high removal efficiency (88%) of As (100 µg/L) was achieved by the MnO2–H2O2 system within 30 min, which differs from conventional adsorption processes that require external mechanical stirring and conventional arsenite (As (III)) oxidation–adsorption processes that require high quantities of oxidants (such as ozone) and specially synthesized adsorbents/catalysts. The high removal efficiency of As (III) by the MnO2–H2O2 system was attributed to the turbulent conditions precipitated by the extensively generated oxygen (O2) from the catalytic decomposition of H2O2, the efficient adsorption of As on the surface of MnO2, and the effective generation of reactive radicals including hydroxyl and superoxide radicals (•OH and •O2−). Moreover, the MnO2 adsorbents before and after As removal were characterized systematically, and the generated radicals were verified using electron spin resonance (ESR). The results showed that the formation of inner-sphere surface complexes by the surface hydroxyl groups of MnO2 particles and As was responsible for the effective As adsorption process, and the oxidation of As (III) to arsenate (As (V)) was achieved via the generated radicals. The influences of representative environmental factors on As removal performance and the application of the MnO2–H2O2 system in river water and ground water were further studied and tested. In conclusion, the MnO2–H2O2 system offers several advantages, including low cost, ease of operation, and strong environmental adaptability, making it highly promising for practical water treatment applications.